Symptom_CUI Symptom_Name Disease_CUI Disease_Name Source C0026821 Cramp C0008626 Congenital chromosomal disease HSDN C0028738 Nystagmus C3805375 Albinism, oculocutaneous, type vi MalaCards C0917801 Sleep disorder insomnia C1561850 Insomnia due to mental disorder UMLS C1963077 Bone pain adverse event C0733682 Hypophosphatemic rickets, x-linked dominant OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0338480 Common migraine HSDN C2984057 Have nausea C1527336 Sjogren's syndrome HSDN C4085222 Nausea C0007786 Brain ischemia HSDN C0036572 Convulsion C0265248 Ruvalcaba syndrome MalaCards C0022346 Yellow skin C0014175 Endometriosis HSDN C1961131 Cough adverse event C0006663 Calcinosis HSDN C4085317 Diarrhea frequency C0005417 Bile duct fistula HSDN C0009806 Constipate C0042781 Visceral myopathy MalaCards|UMLS C1557397 Adverse event associated with pain C0035854 Rosacea HSDN C4084784 Diarrhea C0205788 Histiocytoid hemangioma HSDN C0917816 Deficiency mental C1855788 Ichthyosis with alopecia, eclabion, ectropion, and mental retardation MalaCards C0018784 Deafness sensorineural C3150913 Congenital disorder of glycosylation, type ip MalaCards|HPO C3539896 Pelvic pain occurs with urination C0236969 Substance-related disorders HSDN C0007758 Cerebellar ataxia C1412759 Bckdha gene HSDN C0036572 Convulsion C1849508 Epilepsy, pyridoxine-dependent OrphaNet|UMLS|MalaCards C0002965 Crescendo angina C0007097 Carcinomas HSDN C0031911 Pigment deposition C0031269 Peutz-jeghers syndrome MalaCards C1963137 Hydrocephalus adverse event C0265306 Greig cephalopolysyndactyly syndrome MalaCards|HPO C3829611 Nausea frequency C0026266 Mitral valve insufficiency HSDN C1549543 Administration method - pain C0344479 Spinal cord myelodysplasia HSDN C0028961 Urine output decreased C0010246 Coxsackievirus infections HSDN C0002962 Angina C2936380 Neointima HSDN C3641756 Have diarrhea C1970820 Fabry disease, cardiac variant HPO C0151786 Weakness muscle C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0232461 Increased appetite C0032897 Prader-willi syndrome MalaCards|HPO C0036572 Convulsion C0268425 Alstrom syndrome MalaCards|HPO C0750426 Wbc elevated C3645711 Congenital osteopetrosis MalaCards C0034933 Abnormal reflexes C0006147 Breast fed HSDN C4085549 Dizziness C1090821 Sepsis (invertebrate) HSDN C0349588 Stature short C3160739 Fanconi anemia, complementation group e MalaCards|HPO C0023012 Delay language C3809327 Spinocerebellar ataxia, autosomal recessive 14 MalaCards C0557874 Global developmental delay C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C0012569 Double vision C0032788 Postoperative hemorrhage HSDN C1557397 Adverse event associated with pain C0010481 Cushing syndrome HSDN C4050613 Anxiety C1859252 Cerebrofaciothoracic dysplasia MalaCards C0003126 Smell loss C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease HPO|UMLS C0004604 Pain back C0021841 Intestinal neoplasms HSDN C1961131 Cough adverse event C1175175 Severe acute respiratory syndrome HSDN C1557397 Adverse event associated with pain C0014179 Endometritis HSDN C4084784 Diarrhea C0024138 Lupus erythematosus, discoid HSDN C0235198 Disturbed mental concentration C1850442 Ceroid lipofuscinosis, neuronal, 5 MalaCards C0242936 Center pain C0030422 Extra-adrenal paraganglioma HSDN C0012569 Double vision C0042830 Perception visual HSDN C0003467 Angst C0025268 Multiple endocrine neoplasia type 2a OrphaNet C3898969 Have been vomiting C0341480 Pancreas, cyst, congenital MalaCards C2911645 Weight loss adverse event C0162703 Pain sensitivity HSDN C4084766 Vomiting C0005974 Bone resorption HSDN C0011991 Loose stools C0206754 Neuroendocrine tumors HSDN C4084774 Have weight loss C1306577 Dies patient HSDN C0004093 Asthenia C0020502 Hyperparathyroidism HSDN C3541349 Syncope C0023418 Leukemia HSDN C4084766 Vomiting C1555914 Psychologist - psychotherapy, group HSDN C0013456 Pain ear C0018199 Granuloma, plasma cell HSDN C0009676 Confusion state C0007760 Cerebellar diseases HSDN C0020672 Body temperature decreased C0750394 Wbc low HSDN C0042963 Symptoms vomiting C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C3815497 Cough C0020437 Hypercalcemia HSDN C3274920 Have shortness of breath question C0238990 Acute lower respiratory tract infection MalaCards C4085210 Usual severity pain C0003496 Aortic rupture HSDN C0751495 Seizure focal C0275904 Tuberculosis, central nervous system UMLS C0973461 Dysphasia C3888081 L-2-hydroxyglutaric acidemia MalaCards|HPO C0023014 Developmental disorder language C0949683 Sex chromosome disorders HSDN C0917816 Deficiency mental C1848561 Methylmalonic acidemia with homocystinuria OrphaNet|HPO|MalaCards C0018989 Paresis of one side of body C1847501 Glut1 deficiency syndrome OrphaNet|MalaCards C1579931 Depressed - symptom C2751842 Parkinson disease 14, autosomal recessive MalaCards|HPO C1961131 Cough adverse event C0009241 Cognition disorders HSDN C0043094 Weight gain C1962979 Burn adverse event HSDN C0042024 Urine incontinence C0021799 Interprofessional relations HSDN C0428977 Pulse rate decrease C2940786 Thyroid hormone resistance syndrome HPO C2315100 Pediatric failure to thrive C0043251 Wounds and injuries HSDN C0030486 Extremity paralysis, lower C1963064 Anxiety adverse event HSDN C0010200 Cough symptom C0041234 Chagas disease OrphaNet|MalaCards C0024031 Back pain lower back C0814263 Meditation therapy HSDN C1963063 Anorexia adverse event C0025517 Metabolic diseases HSDN C0036572 Convulsion C0393576 Chorea acanthocytosis syndrome OrphaNet|HSDN|UMLS|HPO|MalaCards C0037763 Spasm C0033975 Psychotic disorders HSDN C0000737 Abdomen pain C3273103 Gallbladder cribriform carcinoma UMLS C0038002 Spleen enlargement C0268312 Progressive intrahepatic cholestasis (disorder) OrphaNet|HPO C0557874 Global developmental delay C3714756 Intellectual disability MalaCards C3541349 Syncope C3501853 Long qt syndrome 1-2 MalaCards C0235153 Sensory hallucination C0276496 Familial alzheimer disease (fad) MalaCards C4085222 Nausea C0021603 Sleep initiation and maintenance disorders HSDN C0036572 Convulsion C0270972 Cornelia de lange syndrome MalaCards|HPO C0042024 Urine incontinence C0497573 Condylomata acuminata in women HSDN C4084802 Usual severity diarrhea C0008519 Ectopic tissue HSDN C4084775 Usual severity weight loss C0011615 Dermatitis, atopic HSDN C0522179 Anxiety death C0003467 Anxiety UMLS C0424755 Fever symptoms C0001511 Tissue adhesions HSDN C0039070 Collapse fleeting C0022658 Kidney diseases HSDN C0013404 Respiratory difficulty C0031046 Pericarditis HSDN C0039070 Collapse fleeting C4023587 Abnormality of cardiovascular system physiology UMLS C3641756 Have diarrhea C0007097 Carcinomas HSDN C3463815 Feel fatigue C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C3146279 Coma C0472377 Basal ganglia hemorrhage HSDN C0241210 Speaking delay C0795949 Galloway mowat syndrome HPO C1963087 Constipation adverse event C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0018991 Paralysis one side of body C0013295 Duodenal ulcer HSDN C2237041 Shox gene with short stature C0342642 Autosomal dominant hypophosphatemic rickets MalaCards|HPO C0497247 Blood pressure elevation C0023195 Lecithin acyltransferase deficiency OrphaNet C0030193 Sense of pain C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C3541349 Syncope C0023903 Liver neoplasms HSDN C4085317 Diarrhea frequency C0011630 Dermatomycoses HSDN C4084773 Bothered by weight gain C0007099 Carcinoma in situ HSDN C4084724 Usual severity constipation C0020598 Hypocalcemia HSDN C4085211 Pain distress question C0013292 Obstruction duodenal HSDN C0349588 Stature short C1850568 Nakajo syndrome MalaCards|HPO C0015672 Decreased energy C0919267 Ovarian neoplasm HSDN C0040034 Thrombocytopenia C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C4085210 Usual severity pain C0016045 Fibroma HSDN C0018808 Murmur C0006288 Bronchopulmonary sequestration HSDN C0034124 Pupillary disorder C0015458 Facial hemiatrophy HSDN C4084773 Bothered by weight gain C0233629 Thinking and speaking disturbances HSDN C0015230 Exanthem C2733483 Masters disease UMLS C0233794 Memory impaired C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C0020672 Body temperature decreased C0018213 Graves disease HSDN C0009792 Consciousness disorder C0025293 Meningitis, listeria HSDN C3809715 Epistaxis recurrent C0040034 Thrombocytopenia UMLS C0262384 Chest pain atypical C0085762 Alcohol abuse UMLS C2936821 Spinal cerebrospinal fluid leak C0027794 Neural tube defects HSDN C1384666 Decreased hearing C0027412 Opioid-related disorders HSDN C0013595 Eczematous dermatitis C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0017181 Gastrointestinal bleed C0019069 Hemophilia a MalaCards C0557874 Global developmental delay C3150801 Combined oxidative phosphorylation deficiency 7 MalaCards|HPO C0034150 Skin purpura C0030326 Panniculitis HSDN C1963281 Vomiting adverse event C0027583 Nematode infections HSDN C0557874 Global developmental delay C2675179 Arginine:glycine amidinotransferase deficiency MalaCards|HPO C0010200 Cough symptom C1963198 Pancreatitis adverse event HSDN C0042024 Urine incontinence C0019555 Hip dislocation, congenital HSDN C0030554 Abnormal sensation C0005695 Bladder neoplasm HSDN C0232466 Feeding difficulty C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0030193 Sense of pain C3714644 Thymus neoplasms HSDN C4085548 Usual severity dizziness C0007570 Celiac disease HSDN C0042940 Disorder of voice C0019693 Hiv infections HSDN C0000737 Abdomen pain C1336008 Small intestinal small cell carcinoma UMLS C0234132 Pyramidal sign C1858114 Huntington disease-like 3 (disorder) MalaCards|UMLS C0344315 Mood depressed C1527168 Bonnevie-ullrich syndrome MalaCards C4084769 Vomiting frequency C0001314 Acute disease HSDN C0005745 Blepharoptosis C0029411 Osteoarthropathy, primary hypertrophic MalaCards|HPO C1579931 Depressed - symptom C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C1963093 Dizziness adverse event C0006736 Body stone HSDN C0035229 Respiratory function impaired C0079541 Holoprosencephaly MalaCards C3641756 Have diarrhea C0152101 Hypoplastic left heart syndrome HSDN C3887638 Failure to thrive in infant C1801959 Histiocytic medullary reticulosis (disorder) MalaCards|HPO C4084766 Vomiting C0037199 Sinusitis HSDN C3539890 Pelvic pain causes awakening at night C0269185 Uterus retroverted HSDN C0242936 Center pain C0008088 Child psychiatry HSDN C0086437 Joint hypermobility C2713392 Phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency HPO C0033377 Caudal displacement C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C0033775 Anal pruritus C1302789 Disorder of perianal skin UMLS C4085210 Usual severity pain C0020514 Hyperprolactinemia HSDN C0012833 Dizzy C0038454 Cerebrovascular accident HSDN C1549543 Administration method - pain C0043540 Zygomatic fracture HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0007785 Cerebral infarction HSDN C0033377 Caudal displacement C1838625 Warburg sjo fledelius syndrome HPO C4084768 Usual severity vomiting C0042035 Urination disorders HSDN C0015230 Exanthem C0220754 Biotinidase deficiency MalaCards|HPO|UMLS C0518090 Frequency of pain question C0027927 Neurosyphilis HSDN C0019572 Hairiness C2700425 Ehlers-danlos syndrome, dermatosparaxis type HPO C4085211 Pain distress question C0007350 Cat disease HSDN C2911647 Weight gain adverse event C1136321 Hiv-associated lipodystrophy syndrome HSDN C0030554 Abnormal sensation C0037937 Spine injury HSDN C0010520 Skin cyanosis C0042138 Uterine neoplasms HSDN C0234146 Absent reflex C1849386 Myoglobinuria, acute recurrent, autosomal recessive MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0029294 Orofaciodigital syndromes MalaCards C1836296 Lower extremity weakness C4225171 Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration UMLS C0020578 Hyperventilate C0023903 Liver neoplasms HSDN C0557874 Global developmental delay C2676766 Osteopetrosis, autosomal recessive 7 MalaCards|HPO C4085211 Pain distress question C2936490 Cardiac arrest, out-of-hospital HSDN C4020887 Photodysphoria C1636149 Macular dystrophy, corneal type 1 HPO C0424755 Fever symptoms C0149778 Soft tissue infections HSDN C0278152 Hemifacial spasms C0042594 Vestibular diseases HSDN C1963087 Constipation adverse event C0035242 Respiratory tract diseases HSDN C4084775 Usual severity weight loss C0041312 Tuberculosis git nos DiseaseOntology|HSDN|MalaCards C0241210 Speaking delay C0751667 Canavan disease, juvenile OrphaNet|HPO C4084784 Diarrhea C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C3463815 Feel fatigue C0679360 Foodborne disease HSDN C0751495 Seizure focal C0014556 Epilepsy, temporal lobe UMLS C0003962 Ascites C0342853 Sialuria OrphaNet|MalaCards C0497406 Over weight C0038395 Streptococcal infections HSDN C2984058 Have pain C0015408 Eye injury HSDN C0020305 Fetal edema C0235833 Congenital diaphragmatic hernia HSDN C0005745 Blepharoptosis C1847800 Waardenburg syndrome type 1 MalaCards|HPO C4085642 Level of joint stiffness C1859709 Kuskokwim disease OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0005417 Bile duct fistula HSDN C4085642 Level of joint stiffness C0152085 Post-dysenteric reactive arthropathy nos MalaCards C4084776 Weight loss C0153653 Malignant tumor of parathyroid gland MalaCards C0000737 Abdomen pain C4085311 Depression - recess HSDN C2032395 Pelvic pain on the left C0520676 Premenstrual dysphoric disorder HSDN C0018777 Deafness, conductive C1857576 Contractures, congenital, torticollis, and malignant hyperthermia MalaCards C4084802 Usual severity diarrhea C1135821 Mortality syndrome, spiking HSDN C4085317 Diarrhea frequency C0010346 Crohn disease MalaCards C0085631 Abnormal excitement C1963138 Hypertension adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1299919 Enteric coccidiosis HSDN C3665347 Vision impaired C0730290 Cone dystrophy MalaCards C0018681 Headache, cephalalgia C0006736 Body stone HSDN C0086565 Liver function abnormal C1720862 Congenital generalized lipodystrophy type 1 MalaCards C0022568 Inflammation corneal C3887525 Keratosis follicularis spinulosa decalvans, x-linked MalaCards C0009806 Constipate C0016658 Fracture bone HSDN C0035021 Fever, famine C0040830 Fever, five-day DiseaseOntology|MalaCards C0085631 Abnormal excitement C0027651 Tumor HSDN C0034933 Abnormal reflexes C0025160 Megacolon HSDN C0917816 Deficiency mental C1859487 Biemond syndrome ii MalaCards C4050613 Anxiety C1857844 Williams-beuren region duplication syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C0036221 Mast-cell sarcoma HSDN C1999266 Depression adverse event C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0750394 Wbc low C0024143 Lupus nephritis MalaCards C0020538 Hbp C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C0036572 Convulsion C1332969 Childhood ganglioglioma UMLS C3463815 Feel fatigue C0018794 Heart block HSDN C0018681 Headache, cephalalgia C0003125 Anorexia nervosa HSDN C0398650 Idiopathic thrombocytopenia purpura C0007097 Carcinomas HSDN C0009806 Constipate C0020676 Hypothyroidism HSDN|UMLS C0018965 Blood urine C1274795 Urban schosser spohn syndrome MalaCards C0007758 Cerebellar ataxia C1848932 Tapetoretinal degeneration with ataxia MalaCards C0850758 Pain pelvic C0206654 Leiomyomatosis HSDN C3815497 Cough C0524688 Pneumonic plague DiseaseOntology|MalaCards C0013404 Respiratory difficulty C1335325 Papillary lung adenocarcinoma UMLS C1963071 Back pain adverse event C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1527344 Dysphonia C1837541 Spinocerebellar ataxia 20 MalaCards C0018524 Hallucinate C0751276 Metachromatic leukodystrophy, juvenile type HPO C4084774 Have weight loss C1854182 Parkinson disease 4, autosomal dominant lewy body (disorder) HPO C0750394 Wbc low C0019097 Hemorrhagic fever, argentinian MalaCards C4084776 Weight loss C0524801 Retinal neoplasms HSDN C0424755 Fever symptoms C0751878 Vasculitis, central nervous system HSDN C3203358 Alveolar hypoventilation C0027404 Narcolepsy HSDN C1963091 Diarrhea adverse event C0007138 Carcinoma, transitional cell HSDN C2236754 Abdominal pain of childhood C2103077 Disorder of jejunum and ileum UMLS C1963087 Constipation adverse event C0268407 Senile cardiac amyloidosis MalaCards C0013421 Dystonia C0023895 Liver diseases HSDN C1971624 Appetite absent C0341480 Pancreas, cyst, congenital MalaCards C4085661 Usual severity nausea C0018824 Heart valve disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0022336 Creutzfeldt-jakob disease HSDN C0151908 Dry skin C1563716 Thyroid dysgenesis HPO C4085317 Diarrhea frequency C0242350 Erectile dysfunction HSDN C1384606 Dyspareunia C0242342 Sheehan syndrome OrphaNet|MalaCards C0011168 Disorder deglutition C3554209 Pontocerebellar hypoplasia, type 8 MalaCards C1971624 Appetite absent C2984289 Melanoma pathway HSDN C0009806 Constipate C0949135 Other constipation UMLS C0206146 Myocardial stunning C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084768 Usual severity vomiting C0024437 Macular degeneration HSDN C1519353 Skin eruption papular C0004943 Behcet syndrome OrphaNet|HPO|MalaCards C0522224 Palsied C0010674 Cystic fibrosis HSDN C0009806 Constipate C0027651 Tumor HSDN|UMLS C0018784 Deafness sensorineural C2675302 Kallmann syndrome 5 MalaCards C0028738 Nystagmus C1843920 Coenzyme q10 deficiency HPO C0007166 Cardiac output decreased C0001430 Adenoma HSDN C1963071 Back pain adverse event C0018934 Hematocolpos HSDN C0018777 Deafness, conductive C0005940 Bone diseases HSDN C0011991 Loose stools C0042900 Vitiligo HSDN C0042963 Symptoms vomiting C0405083 Mild hyperemesis unspecified UMLS C0162298 Stiffness joints C1844887 Catel manzke syndrome OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0003850 Arteriosclerosis HSDN C0578056 Pain of truncal structure C0452160 Lumbago; sciatica UMLS C0150055 Pain chronic C0001807 Aggressive behavior HSDN C1384666 Decreased hearing C0796147 Acrocallosal syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0004161 Athletic injuries HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003864 Arthritis HSDN C4084802 Usual severity diarrhea C0023420 Mouse leukemia l1210 HSDN C1963184 Nystagmus adverse event C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO C0003079 Pupillary inequality C0339289 Injury corneal HSDN C2024893 Cardiovascular surgery result: fatigue C0268251 Gaucher disease, type 3 (disorder) OrphaNet|HPO|MalaCards C0008031 Pain chest C0022658 Kidney diseases HSDN C0013604 Edematous C3249880 Solar erythema HSDN C0005745 Blepharoptosis C1855477 Dahlberg borer newcomer syndrome MalaCards C0035229 Respiratory function impaired C0265220 Pallister-hall syndrome MalaCards C0037316 Not enough sleeping C0008073 Developmental disabilities HSDN C3146279 Coma C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C4084769 Vomiting frequency C1532560 Plasmacytoma - category HSDN C0162834 Hyperpigmentation C1865616 Hemochromatosis, type 2b MalaCards C0032285 Pneum C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C0004134 Dyssynergia C0162672 Merrf syndrome OrphaNet|HPO|MalaCards C3274924 Have been coughing C0040411 Tongue neoplasms HSDN C2029884 Hearing loss by exam C0019163 Hepatitis b HSDN C3665346 Loss sight C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0018784 Deafness sensorineural C0032584 Polyps HSDN C3539895 Pelvic pain occurs with bowel movement C0004936 Mental disorders HSDN C1384666 Decreased hearing C0029422 Osteochondrodysplasias HSDN C0234146 Absent reflex C1854150 Charcot-marie-tooth disease, type 2b2 HPO C0000737 Abdomen pain C0007820 Cerebrovascular disorders HSDN C1963071 Back pain adverse event C0042580 Vesico-ureteral reflux HSDN C0917816 Deficiency mental C3151355 Megalencephalic leukoencephalopathy with subcortical cysts 2a MalaCards|HPO C0221166 Paraparesis C3495801 Granulomatosis with polyangiitis HSDN C4084784 Diarrhea C1333764 Gastric cronkhite canada polyposis MalaCards C4084776 Weight loss C0028738 Nystagmus HSDN C4085222 Nausea C0021295 Infant, premature, diseases HSDN C0151311 Cranial nerve palsy C0268250 Gaucher disease, type 2 (disorder) MalaCards C0019825 Voice hoarseness C0020725 Type ii mucolipidosis MalaCards|HPO C4084725 Usual severity cough C0021818 Intervertebral disk displacement HSDN C1962972 Proteinuria adverse event C0043398 Yellow fever, urban MalaCards C0009806 Constipate C0878683 Pituitary dwarfism type 3 MalaCards C0015672 Decreased energy C1879338 Bereavement, life event HSDN C0234132 Pyramidal sign C2677589 Spinocerebellar ataxia, autosomal recessive 9 MalaCards|HPO C0042928 Paralysis vocal cord C0003469 Anxiety disorders HSDN C0010200 Cough symptom C1336233 Stage iiib squamous cell carcinoma of lung UMLS C0018681 Headache, cephalalgia C0032238 Bornholm disease DiseaseOntology|MalaCards C0030193 Sense of pain C1412084 Abcd1 gene HSDN C0557874 Global developmental delay C2931646 Oculocerebral hypopigmentation syndrome type preus OrphaNet|MalaCards C1963274 Vasculitis adverse event C2873856 Essential cryoglobulinemia MalaCards C4042891 Sleep wake disorders C0004238 Atrial fibrillation HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C1834144 Sick sinus syndrome 2, autosomal dominant MalaCards C4084724 Usual severity constipation C0453996 Tobacco smoking HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038273 Stereotypic movement disorder HSDN C3665347 Vision impaired C4015388 Mccrp2 MalaCards C4085317 Diarrhea frequency C0032965 Pregnancy complications, infectious HSDN C2911647 Weight gain adverse event C0013010 Cerebral lateralization HSDN C1279888 Proteinuria of undiagnosed cause C0021368 Inflammation HSDN C4085211 Pain distress question C0162834 Hyperpigmentation HSDN C4085317 Diarrhea frequency C0042075 Urologic diseases HSDN C0002965 Crescendo angina C0032227 Pleural effusion disorder HSDN C0151786 Weakness muscle C1856058 Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity HPO|UMLS C2919142 Short stature adverse event C2936921 Saccharopine dehydrogenase deficiency MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0026766 Multiple organ failure HSDN C4042891 Sleep wake disorders C0024408 Machado-joseph disease HSDN C0042963 Symptoms vomiting C1510426 Choroid plexus carcinoma, childhood UMLS C1963252 Tremor adverse event C1857662 Coach syndrome MalaCards|HPO C1963071 Back pain adverse event C0085183 Neoplasms, second primary HSDN C0026838 Spasticity muscle C0011334 Dental caries HSDN C0027498 Nausea vomiting C1707400 Classic medulloblastoma MalaCards C0578055 Pain of head and neck region C0522255 Cervical root pain UMLS C0026838 Spasticity muscle C0268540 Hhh syndrome UMLS C0018681 Headache, cephalalgia C1266119 Solitary fibrous tumor HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001122 Acidosis HSDN C0007859 Pain neck C0014859 Esophageal neoplasms HSDN C0013362 Dysarthrias C0271001 Siderosis of eye HSDN C2237041 Shox gene with short stature C3809233 Noonan syndrome 8 MalaCards C4084802 Usual severity diarrhea C0020255 Hydrocephalus HSDN C0037316 Not enough sleeping C0022658 Kidney diseases HSDN C0232466 Feeding difficulty C1850055 Peho syndrome OrphaNet|HPO|MalaCards C0234979 Dysdiadochokinesia C3280977 Spastic ataxia 5, autosomal recessive UMLS C0231528 Muscle pain generalized C0019655 Histoplasmosis MalaCards C0162835 Hypopigmentation C0162635 Angelman syndrome MalaCards|HPO C0004093 Asthenia C0221018 Hereditary sideroblastic anemia HSDN C4085548 Usual severity dizziness C0022865 Obstetric labor complications HSDN C0043094 Weight gain C0012979 Canine disease HSDN C3887873 Hearing loss C0270612 Leukoencephalopathies HSDN C0277959 Hair coarseness C1851710 Lateral meningocele syndrome MalaCards|HPO C4085317 Diarrhea frequency C0014009 Empyema HSDN C2024878 Cardiovascular surgery result: dyspnea C0040124 Thyroglossal duct cyst HSDN C2024878 Cardiovascular surgery result: dyspnea C2240378 Cleft palate on exam HSDN C0497406 Over weight C0034885 Rectal neoplasms HSDN C0022107 Fussiness C1839530 Valproate sensitivity HPO C4084776 Weight loss C0585442 Osteosarcoma of bone HSDN C2029884 Hearing loss by exam C0042018 Urinary calculi HSDN C3887638 Failure to thrive in infant C3280314 Combined malonic and methylmalonic aciduria MalaCards C0027796 Neuralgias C1963137 Hydrocephalus adverse event HSDN C4085222 Nausea C0004692 Balantidiasis MalaCards C0003862 Pain joint C0086922 Purpura rheumatoid OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0752235 Lyme neuroborreliosis DiseaseOntology|HSDN|MalaCards C1557397 Adverse event associated with pain C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C1384666 Decreased hearing C0006131 Branchioma HSDN C1962972 Proteinuria adverse event C0024110 Pulmonary abscess HSDN C0032617 High urine output C0268080 Hypercalcemia, idiopathic, of infancy HPO C0009398 Color vision defects C1860406 Vitreoretinochoroidopathy (disorder) MalaCards|HPO C0011168 Disorder deglutition C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards C2024878 Cardiovascular surgery result: dyspnea C0162820 Dermatitis, allergic contact HSDN C0151786 Weakness muscle C0037304 Skull fracture HSDN C2242996 Tingling C0001418 Adenocarcinoma HSDN C0011168 Disorder deglutition C2931821 Nakamura osame syndrome MalaCards C0013390 Cramps menstrual C0232488 Abdominal colic HSDN C4085210 Usual severity pain C0033999 Pterygium HSDN C4085210 Usual severity pain C1636667 Disorder characterized by eosinophilia HSDN C4085862 Bothered by nausea C0015397 Disorder of eye HSDN C0023012 Delay language C0004352 Autistic disorder HPO C0000727 Abdomen acute C0031542 Phlebitis HSDN C4085210 Usual severity pain C0032708 Disorders of porphyrin metabolism HSDN C0027497 Queasy C0085278 Antiphospholipid syndrome HSDN C0011991 Loose stools C0023895 Liver diseases HSDN C0010200 Cough symptom C0038587 Substance withdrawal syndrome HSDN C2096293 Ent surgical result ear vertigo C3810814 Myocardial infarction ecg assessment HSDN C2984058 Have pain C0038018 Spondylolysis HSDN C0030552 Paralysis partial C0026269 Mitral valve stenosis HSDN C2024878 Cardiovascular surgery result: dyspnea C0042345 Varicosity HSDN C2984057 Have nausea C0032131 Plasmacytoma HSDN C1963071 Back pain adverse event C0032226 Pleural diseases HSDN C0003862 Pain joint C0016663 Pathological fracture HSDN C0030486 Extremity paralysis, lower C0011303 Demyelinating diseases HSDN C0042571 Vertigo subjective C0086957 Naffziger syndrome HSDN C0018772 Deafness C3540662 Congenital amaurosis of retinal origin MalaCards C0031911 Pigment deposition C0334092 Hamartomatous polyp MalaCards C4084769 Vomiting frequency C0040156 Thyrotoxicosis HSDN C0848203 Male pelvic pain C0012979 Canine disease HSDN C0027497 Queasy C0022104 Irritable bowel syndrome HSDN C0878773 Bladder hyperactive C0393571 Multiple system atrophy HSDN C0231218 Malaise generalized C0345905 Intrahepatic cholangiocarcinoma UMLS C3641756 Have diarrhea C1135821 Mortality syndrome, spiking HSDN C4084769 Vomiting frequency C0022602 Actinic keratosis HSDN C4084776 Weight loss C0206743 Rhabdoid tumor OrphaNet|MalaCards C0518090 Frequency of pain question C0016978 Gallbladder neoplasm HSDN C4084766 Vomiting C0011875 Diabetic angiopathies HSDN C0009398 Color vision defects C0393807 Hereditary motor and sensory neuropathy with optic atrophy (disorder) HPO C0030552 Paralysis partial C4048184 Trochlear nerve diseases HSDN C2315100 Pediatric failure to thrive C0796002 Johnson-mcmillin syndrome MalaCards C2911647 Weight gain adverse event C0021845 Intestinal perforation HSDN C0848203 Male pelvic pain C1456865 Ureteral calculi HSDN C4085862 Bothered by nausea C0029823 Other specif.peritonitis nos DiseaseOntology C3163620 Hypotension adverse event C0268293 Corticosterone methyl oxidase type i deficiency HPO C0518090 Frequency of pain question C1963234 Serum sickness adverse event HSDN C0151889 Reflexes tendon increased C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO C4085661 Usual severity nausea C0011875 Diabetic angiopathies HSDN C0700590 Diaphoresis excessive C0079299 Epidermolysis bullosa simplex kobner OrphaNet|HPO C1963180 Neck pain adverse event C0314657 Genetic predisposition HSDN C0233769 Lilliputian hallucination C1720077 Micropsia due to organic disease UMLS C4042891 Sleep wake disorders C1963090 Dehydration adverse event HSDN C1962972 Proteinuria adverse event C0021843 Intestinal obstruction HSDN C0003862 Pain joint C1366464 F9 gene HSDN C0018784 Deafness sensorineural C3553349 Coenzyme q10 deficiency, primary, 6 MalaCards C3829611 Nausea frequency C1963064 Anxiety adverse event HSDN C0036572 Convulsion C0393700 Cryptogenic lennox-gastaut syndrome UMLS C4084725 Usual severity cough C0403447 Chronic kidney insufficiency HSDN C4084774 Have weight loss C0016977 Gall bladder diseases HSDN C0003079 Pupillary inequality C0022079 Iris neoplasms HSDN C0030193 Sense of pain C0016665 Fracture, nos with nonunion HSDN C4084766 Vomiting C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards C3541349 Syncope C0036341 Schizophrenia HSDN C3539895 Pelvic pain occurs with bowel movement C1881674 Medical device emits smoke HSDN C0521815 Vertigo preceded by head injury C0271487 Vertiginous disorder UMLS C0557874 Global developmental delay C3150672 Arthrogryposis, renal dysfunction, and cholestasis 2 MalaCards|HPO C0242936 Center pain C0334409 Leydig cell tumor, benign HSDN C0033377 Caudal displacement C3711158 Metatropic dwarfism, type ii MalaCards C0019825 Voice hoarseness C0018523 Hallervorden-spatz syndrome MalaCards|HPO C0000737 Abdomen pain C0279639 Mucinous adenocarcinoma of the colon UMLS C0004134 Dyssynergia C0002395 Alzheimer's disease HSDN C0006370 Bulimia C0010346 Crohn disease HSDN C3665346 Loss sight C1847197 Vascular malformation, primary intraosseous MalaCards C4084769 Vomiting frequency C0033953 Psychosexual disorders HSDN C0036572 Convulsion C1550639 Specimen type - fistula HSDN C0030794 Pelvis pain C0015732 Fecal incontinence HSDN C0004604 Pain back C0003125 Anorexia nervosa HSDN C0042963 Symptoms vomiting C0020625 Hyponatremia HSDN|UMLS C3887638 Failure to thrive in infant C2675891 Chromosome 1q21.1 duplication syndrome MalaCards C2315100 Pediatric failure to thrive C0008065 Childhood behavior HSDN C4084724 Usual severity constipation C0030521 Parathyroid neoplasms MalaCards C1961131 Cough adverse event C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0035229 Respiratory function impaired C0342720 Adenosylcobalamin synthesis defect MalaCards C0751401 Ophthalmoparesis C0010324 Crigler najjar syndrome, type 1 MalaCards C0522224 Palsied C0030922 Peptic ulcer hemorrhage HSDN C0030193 Sense of pain C0347895 Neuralgia, neuritis or radiculitis nos UMLS C4084767 Bothered by vomiting C0024692 Mandible fracture HSDN C4085317 Diarrhea frequency C0025149 Medulloblastoma HSDN C0015402 Hemorrhage eye C0460136 Barotrauma HSDN C0013395 Indigestion C0014858 Esophageal motility disorders UMLS C4084766 Vomiting C0005695 Bladder neoplasm HSDN C1961131 Cough adverse event C0279628 Adenocarcinoma of esophagus OrphaNet C1963087 Constipation adverse event C0342257 Complications of diabetes mellitus HSDN C0812426 Kidney problem C0403468 Papillary necrosis acute UMLS C0031911 Pigment deposition C0206739 Epithelioid and spindle cell nevus MalaCards C2024893 Cardiovascular surgery result: fatigue C0015618 Families therapy HSDN C0037316 Not enough sleeping C0043251 Wounds and injuries HSDN C1963091 Diarrhea adverse event C1963709 Abetalipoproteinemia (lab finding) HSDN C2911645 Weight loss adverse event C0010418 Cryptosporidiosis DiseaseOntology|HSDN C0018834 Brash C0341106 Eosinophilic esophagitis OrphaNet|MalaCards C1963137 Hydrocephalus adverse event C2931009 Congenital disorder of glycosylation type 2d OrphaNet|HPO|MalaCards C0040034 Thrombocytopenia C0221013 Mastocytosis, systemic OrphaNet|MalaCards C4084727 Cough frequency C0040046 Thrombophlebitis HSDN C0413252 Hypothermia due to exposure C0024115 Lung diseases HSDN C0043094 Weight gain C0018799 Heart diseases HSDN C0030193 Sense of pain C0232944 Secondary dysmenorrhoea UMLS C4084775 Usual severity weight loss C0039981 Thoracic neoplasms HSDN C0015672 Decreased energy C0027127 Myotonia congenita HSDN C2024878 Cardiovascular surgery result: dyspnea C0034074 Infarct pulmonary HSDN C0030193 Sense of pain C0018378 Guillain-barre syndrome HSDN C2919142 Short stature adverse event C1832702 Brachydactyly, type a2 MalaCards|HPO C3641756 Have diarrhea C1334928 Necrotic changes (finding) HSDN C0518090 Frequency of pain question C0036349 Paranoid schizophrenia HSDN C2096293 Ent surgical result ear vertigo C0024535 Malaria, falciparum HSDN C1962972 Proteinuria adverse event C0032964 Pregnancy complications, hematologic HSDN C0009806 Constipate C0020538 Hypertensive disease UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C3714644 Thymus neoplasms OrphaNet|HSDN|MalaCards C3641756 Have diarrhea C0036093 Salivary gland diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0235146 Emotionally high HSDN C0009421 Comatose C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C3815497 Cough C0010823 Cytomegalovirus infections HSDN C0018772 Deafness C0029888 Otitis media purulent HSDN C3665347 Vision impaired C1970848 Phosphoglycerate kinase 1 deficiency MalaCards|HPO C0035229 Respiratory function impaired C0238052 Xanthomatosis, cerebrotendinous MalaCards|HPO C0034151 Hyperglobulinemic purpura C0079294 Epidermolysis bullosa dystrophica HSDN C4084776 Weight loss C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C1962972 Proteinuria adverse event C1290398 Cerebral arterial aneurysm HSDN C2024893 Cardiovascular surgery result: fatigue C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C1963091 Diarrhea adverse event C0271737 Addison's disease due to autoimmunity OrphaNet C1557397 Adverse event associated with pain C0017086 Gangrene HSDN C1963077 Bone pain adverse event C0029401 Osteitis deformans HPO C0020672 Body temperature decreased C0035335 Retinoblastoma HSDN C0038002 Spleen enlargement C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|HPO|MalaCards C1384666 Decreased hearing C2931760 Acrocallosal syndrome, schinzel type MalaCards|HPO C3812171 Bradycardia by ecg finding C1859711 Arthrogryposis multiplex congenita with whistling face MalaCards C3887638 Failure to thrive in infant C0024215 Lymphangiectasis, intestinal MalaCards C0018777 Deafness, conductive C1414899 Gaa gene HSDN C0151889 Reflexes tendon increased C0393559 Troyer syndrome HPO C1963063 Anorexia adverse event C0042076 Urologic neoplasms HSDN C1962972 Proteinuria adverse event C0002453 Amenorrhea HSDN C0015672 Decreased energy C0021841 Intestinal neoplasms HSDN C3539023 Pelvic pain increasing in frequency C0022410 Joint instability HSDN C1961131 Cough adverse event C0025007 Measles DiseaseOntology|HSDN|MalaCards C2029884 Hearing loss by exam C0018939 Hematological disease HSDN C3641755 Have constipation C0717360 Disease lyme vaccine HSDN C3815497 Cough C0021933 Intussusception HSDN C0152227 Tearing excessive C0220620 Gastrointestinal carcinoid tumor MalaCards C0018932 Bright red rectal bleeding C1262481 Eosinophilic gastroenteritis MalaCards C0000737 Abdomen pain C3146250 Stage iii colorectal cancer ajcc v7 UMLS C0020672 Body temperature decreased C0342443 Adrenal cushing's syndrome HSDN C0009421 Comatose C0034885 Rectal neoplasms HSDN C0018681 Headache, cephalalgia C0006849 Oral candidiasis UMLS C3641756 Have diarrhea C1863959 Hyperthyroidism, familial gestational OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0018802 Congestive heart failure HSDN C1069915 Vertigo C0009375 Colonic neoplasms HSDN C0030193 Sense of pain C0018805 Heart injuries HSDN C0013421 Dystonia C3150315 Aicardi-goutieres syndrome 1, autosomal dominant HPO C0015469 Facial paralysis C0026633 Mouth abnormalities HSDN C2700617 Irritation - emotion C0678185 Neonatorum; pemphigus MalaCards C0518090 Frequency of pain question C0700359 Organophosphate poisoning HSDN C2984058 Have pain C3469186 Hemochromatosis, type 1 HSDN C0237326 Defecation pain C2750784 Spastic paraplegia 44, autosomal recessive (disorder) MalaCards|HPO C0037763 Spasm C0033893 Tension headache HSDN C0518090 Frequency of pain question C0242216 Biliary calculi HSDN C2237041 Shox gene with short stature C2745959 Spondyloepiphyseal dysplasia, congenita OrphaNet|HPO C0000737 Abdomen pain C0011265 Presenile dementia HSDN C0242936 Center pain C0038018 Spondylolysis HSDN C4084726 Distress cough C0038661 Suicide HSDN C2237041 Shox gene with short stature C2937419 Chromosome x pentasomy OrphaNet|MalaCards C0018772 Deafness C2911643 Encounter due to family history of osteoporosis HSDN C0234378 Postural tremor C1836148 Supranuclear palsy, progressive, 2 MalaCards|UMLS C0151786 Weakness muscle C0004052 Aspiration of vomitus HSDN C1963093 Dizziness adverse event C0039614 Tetanus HSDN C3829611 Nausea frequency C0205770 Choroid plexus papilloma HPO C1963252 Tremor adverse event C1853578 Neuroferritinopathy MalaCards|HPO C0002622 Amnesias C1960100 Shellfish poisoning HSDN C4084774 Have weight loss C1861329 Spinal canal stenosis HSDN C4085210 Usual severity pain C0039585 Androgen-insensitivity syndrome HSDN C0242936 Center pain C0008519 Ectopic tissue HSDN C0522224 Palsied C0014761 Erythroblastosis, fetal HSDN C0424755 Fever symptoms C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C0004604 Pain back C0038395 Streptococcal infections HSDN C0013604 Edematous C0039006 Swine--diseases HSDN C0026884 Muteness C0033367 Projective techniques HSDN C1963184 Nystagmus adverse event C1853116 Spinocerebellar ataxia, autosomal recessive 8 (disorder) MalaCards|HPO C4084766 Vomiting C0206715 Neoplasms, neuroepithelial HSDN C0024031 Back pain lower back C3463824 Myelodysplastic syndrome HSDN C0023380 Lethargy C0018794 Heart block HSDN C0024031 Back pain lower back C0752130 Spinal cord ischemia HSDN C0028738 Nystagmus C1866504 Photosensitive trichothiodystrophy MalaCards C0003079 Pupillary inequality C0043121 Wernicke encephalopathy HSDN C0851578 Disorder sleep C0004935 Animal ethology HSDN C2237041 Shox gene with short stature C0342731 Deficiency of mevalonate kinase OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C4084723 Constipation C0004933 Behavior modification technique HSDN C0024031 Back pain lower back C0019270 Hernia HSDN C0240715 Perineal lump C2959569 Median raphe cyst of penis UMLS C0700292 Arterial hypoxaemia C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C0424755 Fever symptoms C0025294 Meningococcal meningitis HSDN C0026838 Spasticity muscle C1623041 Breast-fed HSDN C4084788 Have dizziness C0002895 Anemia, sickle cell HSDN C0018784 Deafness sensorineural C1963084 Colitis adverse event HSDN C0008031 Pain chest C0403447 Chronic kidney insufficiency UMLS C0497406 Over weight C0154251 Lipid metabolism disorders HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0019348 Herpes simplex infections HSDN C0332563 Papulae C0019618 Histiocytosis MalaCards C1145670 Failure respiratory C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C4084767 Bothered by vomiting C0026598 Movement perception HSDN C0027066 Myoclonic jerking C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy HPO|UMLS C0413252 Hypothermia due to exposure C0013870 Electroconvulsive shock HSDN C0040034 Thrombocytopenia C1859317 Cataract and cardiomyopathy MalaCards|HPO C1963249 Tinnitus adverse event C0024530 Malaria HSDN C3887638 Failure to thrive in infant C1096902 Infantile sialic acid storage disease HPO C1145670 Failure respiratory C0344679 Atresia; pulmonary vein OrphaNet|MalaCards C2984057 Have nausea C0518449 Control of hip fracture risk HSDN C4084767 Bothered by vomiting C0023434 Chronic lymphocytic leukemia HSDN C0242936 Center pain C0001969 Alcoholic intoxication HSDN C3463815 Feel fatigue C0032229 Pleural neoplasms HSDN C0009421 Comatose C0018099 Gout HSDN C1384666 Decreased hearing C0013261 Duane retraction syndrome MalaCards|HSDN C2911645 Weight loss adverse event C0030305 Pancreatitis HSDN C0349588 Stature short C0221036 Acrodermatitis enteropathica OrphaNet|HPO C4042891 Sleep wake disorders C0015397 Disorder of eye HSDN C0019079 Bloody sputum C0013504 Echinococcosis, hepatic HSDN C4084773 Bothered by weight gain C0008149 Chlamydia infections HSDN C1963252 Tremor adverse event C0003469 Anxiety disorders HSDN C0028961 Urine output decreased C0037286 Skin neoplasms HSDN C0003467 Angst C2931246 Chromosome 17, trisomy 17p11 2 OrphaNet|HPO|MalaCards C0026821 Cramp C0025007 Measles HSDN C4042891 Sleep wake disorders C0205788 Histiocytoid hemangioma HSDN C3898969 Have been vomiting C1960459 Hereditary angioedema with normal c1 esterase inhibitor activity MalaCards C0023015 Language handicap C0018798 Congenital heart defects HSDN C0030193 Sense of pain C1522137 Hypertriglyceridemia result HSDN C0151827 Pain eye C0008698 Maxillary sinusitis chronic HSDN C0151908 Dry skin C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO|UMLS C0557874 Global developmental delay C3809221 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 MalaCards C1557397 Adverse event associated with pain C0003125 Anorexia nervosa HSDN C4084784 Diarrhea C0001430 Adenoma HSDN C4084775 Usual severity weight loss C0031099 Periodontitis HSDN C4084766 Vomiting C1704326 Role - roleclass HSDN C4084788 Have dizziness C0025286 Meningioma HSDN C4084774 Have weight loss C1868594 Perry syndrome OrphaNet|HPO|MalaCards C0011206 Delirium acute C0019196 Hepatitis c HSDN C4085210 Usual severity pain C0033936 Psychoses, alcoholic HSDN C0518090 Frequency of pain question C0030424 Paragonimiasis HSDN C4084769 Vomiting frequency C2931876 Hirschsprung disease 1 MalaCards C0020615 Hypoglycemia nos C0016952 Galactosemias MalaCards C4085211 Pain distress question C0854906 Benign schwannoma MalaCards C2984058 Have pain C1862939 Amyotrophic lateral sclerosis 1 MalaCards C0002962 Angina C0022661 Kidney failure, chronic HSDN C1963252 Tremor adverse event C0022744 Knee injury HSDN C0152459 Striae C1857038 Ehlers-danlos syndrome with platelet dysfunction from fibronectin abnormality MalaCards C0030200 Intractable pain C0877172 Hematoma, epidural, spinal HSDN C0398650 Idiopathic thrombocytopenia purpura C0018378 Guillain-barre syndrome HSDN C0522224 Palsied C0019159 Hepatitis a HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C1865019 Short qt syndrome 2 (disorder) MalaCards C0019572 Hairiness C0006663 Calcinosis HSDN C4084767 Bothered by vomiting C0030319 Panic disorder HSDN C4084774 Have weight loss C1000483 Genus anemia HSDN C2911645 Weight loss adverse event C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C0030552 Paralysis partial C0005745 Blepharoptosis HSDN C1557397 Adverse event associated with pain C3668816 Inflammation of non-human mammary gland HSDN C0024031 Back pain lower back C0042018 Urinary calculi HSDN C4084727 Cough frequency C2981150 Uranostaphyloschisis HSDN C3539892 Pelvic pain in front C0026769 Multiple sclerosis HSDN C0011991 Loose stools C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0231341 Aging premature C1690964 Cataract HSDN C3898969 Have been vomiting C0008924 Cleft lip HSDN C0241165 Skin thickening C0342681 Minimal pigment oculocutaneous albinism MalaCards C0007815 Cerebrospinal fluid rhinorrhoea C0206731 Angiofibroma HSDN C4085210 Usual severity pain C0007781 Intracranial embolism and thrombosis HSDN C4084802 Usual severity diarrhea C0035220 Respiratory distress syndrome, newborn HSDN C0003550 Broca aphasia C4084909 Depression subordinate domain HSDN C4084769 Vomiting frequency C0004277 Tooth attrition HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023869 Lithiasis HSDN C4084726 Distress cough C1956390 Cranial arteritis MalaCards C0003811 Cardiac rhythm disturbance C0006035 Borrelia infections MalaCards C0000737 Abdomen pain C0235833 Congenital diaphragmatic hernia HSDN C0018681 Headache, cephalalgia C1960870 Transformed migraine UMLS C0015468 Face pain C0027531 Neck injury HSDN C3641756 Have diarrhea C0034013 Precocious puberty HSDN C0015300 Ocular proptosis C1861922 Campomelic dysplasia OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0017181 Gastrointestinal hemorrhage HSDN C0020673 Hypothermia (central) (local) C0027659 Neoplasms, experimental HSDN C4085222 Nausea C0242350 Erectile dysfunction HSDN C3641755 Have constipation C0014836 Escherichia coli infections HSDN C0018834 Brash C3806688 Congenital disorder of glycosylation, type iim MalaCards C0460137 Push down or depress C3554605 Mc3dn2 MalaCards C0015468 Face pain C0302148 Blood clot HSDN C3641756 Have diarrhea C1962986 Glaucoma adverse event HSDN C0015230 Exanthem C0085399 Ehrlichiosis DiseaseOntology|MalaCards C4084767 Bothered by vomiting C0021828 Intestinal atresia HSDN C0042025 Urinary incontinence stress C0039231 Tachycardia HSDN C0030552 Paralysis partial C0027873 Neuromyelitis optica HSDN C1961131 Cough adverse event C0032290 Aspiration pneumonia MalaCards C0151908 Dry skin C3493776 Hypothyroidism, congenital, nongoitrous, 1 MalaCards C0002622 Amnesias C1762616 Meningioma, benign, no icd-o subtype HSDN C4084802 Usual severity diarrhea C0018671 Head and neck neoplasms HSDN C0917816 Deficiency mental C0010324 Crigler najjar syndrome, type 1 MalaCards|HPO C0151908 Dry skin C1859468 Bird headed dwarfism montreal type OrphaNet|MalaCards C0851578 Disorder sleep C1527429 Increased blood npn HSDN C0018777 Deafness, conductive C0085437 Meningitis, bacterial HSDN C1000483 Genus anemia C0036202 Sarcoidosis MalaCards C3665346 Loss sight C1853959 Birdshot chorioretinopathy OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0036420 Localized scleroderma HSDN C2700617 Irritation - emotion C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C1548578 Location characteristic id - smoking HSDN C0587050 Lower extremity mass C0346451 Neoplasm of lower limb UMLS C2024878 Cardiovascular surgery result: dyspnea C0032019 Pituitary neoplasms HSDN C0150055 Pain chronic C0027609 Neonatal abstinence syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0006434 Burn injury HSDN C1963252 Tremor adverse event C1854336 Paragangliomas 3 MalaCards C4084767 Bothered by vomiting C0000809 Abortion, habitual HSDN C0700590 Diaphoresis excessive C1836010 Spastic paraplegia, optic atrophy, and neuropathy MalaCards|HPO C4084776 Weight loss C0035412 Rhabdomyosarcoma HSDN C1963091 Diarrhea adverse event C0080178 Spina bifida HSDN C2032395 Pelvic pain on the left C1394494 Cystocele, unspecified HSDN C0162298 Stiffness joints C2931421 Brachytelephalangy characteristic facies kallmann OrphaNet|MalaCards C0035078 Failure kidney C1851347 Familial mediterranean fever, autosomal dominant HPO C0750937 Appendicular ataxia C0024748 Alpha-mannosidosis HPO C0009421 Comatose C1865323 Migraine, familial basilar HPO C1963065 Apnea adverse event C0041327 Tuberculosis, pulmonary HSDN C1963137 Hydrocephalus adverse event C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C1000483 Genus anemia C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C3898969 Have been vomiting C0023418 Leukemia HSDN C0028961 Urine output decreased C4049644 Depression HSDN C1510417 Apraxia of gait C0037926 Compression of spinal cord HSDN C0035229 Respiratory function impaired C0036069 Saldino-noonan syndrome MalaCards C0349588 Stature short C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0004763 Barrett esophagus HSDN C3539023 Pelvic pain increasing in frequency C0026769 Multiple sclerosis HSDN C4085211 Pain distress question C0017525 Giant cell tumors HSDN C0042963 Symptoms vomiting C0278599 Cns tumor, childhood infratentorial ependymoma UMLS C0027796 Neuralgias C0039978 Thoracic diseases HSDN C0221166 Paraparesis C0206663 Neuroectodermal tumor, primitive HSDN C1963249 Tinnitus adverse event C0376527 Neoplasm, skull base HSDN C0028738 Nystagmus C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C3463815 Feel fatigue C0524910 Hepatitis c, chronic MalaCards C0473384 Edema or excessive weight gain in pregnancy without mention of hypertension, delivered with mention of postpartum complication C0269672 Weight gain pregnancy excessive UMLS C0349588 Stature short C1855057 Ataxia-telangiectasia variant v2 HPO C2362324 Pediatric obesity C1285666 Drinking behavior HSDN C0030552 Paralysis partial C3554055 Peroxisome biogenesis disorder 14b MalaCards C0497247 Blood pressure elevation C2609260 Caudal dysplasia syndrome HPO C4084775 Usual severity weight loss C0011603 Dermatitis HSDN C0013604 Edematous C0002726 Amyloidosis HSDN C0030193 Sense of pain C0236736 Cocaine-related disorders HSDN C3463815 Feel fatigue C0005940 Bone diseases HSDN C4085548 Usual severity dizziness C0014836 Escherichia coli infections HSDN C0042024 Urine incontinence C0997768 Glaucoma HSDN C0004134 Dyssynergia C0020179 Huntington disease HSDN C2029884 Hearing loss by exam C0012236 Digeorge syndrome HSDN C1384666 Decreased hearing C0007820 Cerebrovascular disorders HSDN C0009792 Consciousness disorder C0853698 Lymphocytes increased HSDN C0003862 Pain joint C0087031 Juvenile-onset still disease OrphaNet|HPO|MalaCards C0557874 Global developmental delay C2931005 Congenital disorder of glycosylation type 1k OrphaNet|HPO|MalaCards C0233763 Hallucinations visual C2931906 Autosomal dominant diffuse lewy body disease MalaCards C0034151 Hyperglobulinemic purpura C0023530 Leukopenia HSDN C0010038 Corneal opacity disorder C2931390 Anophthalmia, cleft lip-palate, facial anomalies, and cns anomalies and hypothalamic disorder MalaCards C0030552 Paralysis partial C0238096 Embolism, paradoxical HSDN C0013362 Dysarthrias C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C1557397 Adverse event associated with pain C0027401 Narcissism HSDN C0030486 Extremity paralysis, lower C1720777 Functional laterality HSDN C4085862 Bothered by nausea C0019080 Hemorrhage HSDN C2700617 Irritation - emotion C0221036 Acrodermatitis enteropathica HPO C0041657 Consciousness loss C0027773 Nesidioblastosis HSDN C0034933 Abnormal reflexes C0305062 Tetanus toxoids HSDN C3539895 Pelvic pain occurs with bowel movement C0033575 Prostatic diseases HSDN C0007166 Cardiac output decreased C0011265 Presenile dementia HSDN C0018991 Paralysis one side of body C0042138 Uterine neoplasms HSDN C1963093 Dizziness adverse event C1706377 Memory device component HSDN C0020639 Hypoproteinaemia C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C0746674 Muscle weakness generalized C2750537 Myopathy, actin, congenital, with cores HPO C0221752 Rbc urine C3805432 Cob1 MalaCards C1963087 Constipation adverse event C0041296 Tuberculosis HSDN C0015672 Decreased energy C0001726 Affective symptoms HSDN C1384666 Decreased hearing C0339527 Leber congenital amaurosis MalaCards|HSDN|HPO C4085661 Usual severity nausea C0031154 Peritonitis HSDN C0036572 Convulsion C0013261 Duane retraction syndrome MalaCards|HPO C0008031 Pain chest C0750181 Ventricular ectopy bigeminy UMLS C0013404 Respiratory difficulty C0037397 Behavior social HSDN C0042571 Vertigo subjective C1706377 Memory device component HSDN C4085210 Usual severity pain C0020758 Congenital ichthyosis HSDN C0026884 Muteness C1836841 Ceroid lipofuscinosis, neuronal, 9 (disorder) MalaCards C0018784 Deafness sensorineural C0028850 Ocular motility disorders HSDN C0036659 Sensation disorder C0010034 Corneal diseases HSDN C0024031 Back pain lower back C0041188 Pyomyositis, tropical HSDN C3541349 Syncope C0008066 Child behavior disorders HSDN C3814530 Skin vesicle C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C4084723 Constipation C0162283 Nephrogenic diabetes insipidus OrphaNet|HPO C1963091 Diarrhea adverse event C0021568 Bites insect stings HSDN C0518090 Frequency of pain question C0021125 Impulsive behavior HSDN C0035078 Failure kidney C0268381 Primary amyloidosis OrphaNet|MalaCards C4084775 Usual severity weight loss C0153415 Malignant neoplasm of lower third of esophagus MalaCards C2984058 Have pain C0024841 Matrimony, matrimonial HSDN C3665492 Pigmentations C0700501 Congenital nystagmus MalaCards C3829611 Nausea frequency C0024115 Lung diseases HSDN C0000737 Abdomen pain C2987169 Pancreatic serous adenoma UMLS C4084725 Usual severity cough C0027627 Neoplasm metastasis HSDN C4085210 Usual severity pain C0009952 Febrile convulsions HSDN C0004604 Pain back C3178970 Entrapment, pudendal nerve MalaCards C0020673 Hypothermia (central) (local) C0002871 Anemia HSDN C0023530 Leukopenia C3150752 Agammaglobulinemia 4, autosomal recessive HPO C0042963 Symptoms vomiting C1335712 Medulloblastoma recurrent UMLS C2984057 Have nausea C0233629 Thinking and speaking disturbances HSDN C1069915 Vertigo C4050613 Anxiety scale (basc-2) HSDN C0035229 Respiratory function impaired C1276035 Pena-shokeir syndrome type i OrphaNet|HPO|MalaCards C2017083 Medial plantar right forefoot pain C0376524 Branchio-oculo-facial syndrome MalaCards C4085551 Usual severity dry mouth C3276706 Small fiber neuropathy MalaCards C4085211 Pain distress question C0740392 Infarction, middle cerebral artery HSDN C1961131 Cough adverse event C0178282 Hernia of abdominal cavity HSDN C0011570 Monopolar depression C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C2029884 Hearing loss by exam C0001080 Achondroplasia HSDN C1963091 Diarrhea adverse event C0024138 Lupus erythematosus, discoid HSDN C4085210 Usual severity pain C0006325 Bruxism HSDN C0030193 Sense of pain C0041321 Tuberculosis, miliary HSDN C0039070 Collapse fleeting C0039145 Syringomyelia and syringobulbia HSDN C0040822 D tremors C1963067 Atrial fibrillation adverse event HSDN C0027066 Myoclonic jerking C3554226 Pch7 MalaCards C0010200 Cough symptom C0031099 Periodontitis HSDN C0042024 Urine incontinence C0032987 Ectopic pregnancy HSDN C4020887 Photodysphoria C1864877 Csnb, incomplete, autosomal recessive MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C2936631 Complaint, subjective health HSDN C0557874 Global developmental delay C1970269 Choreoathetosis, hypothyroidism, and neonatal respiratory distress HPO C0162298 Stiffness joints C0265279 Kniest dysplasia OrphaNet|HPO|MalaCards C0035232 Diaphragmatic paralysis C0010068 Coronary heart disease HSDN C0398650 Idiopathic thrombocytopenia purpura C0030297 Pancreatic neoplasm HSDN C0020673 Hypothermia (central) (local) C0018809 Heart neoplasm HSDN C0015672 Decreased energy C0023473 Myeloid leukemia, chronic OrphaNet|HPO C0036572 Convulsion C0597109 Nurse's role HSDN C0085593 Chill C0002871 Anemia UMLS C2237041 Shox gene with short stature C0342543 Precocious puberty, central HPO C0010200 Cough symptom C0017178 Gastrointestinal diseases HSDN C4042891 Sleep wake disorders C0027412 Opioid-related disorders HSDN C0242936 Center pain C0018572 Hand, foot and mouth disease HSDN C1000483 Genus anemia C0079683 Herlitz disease MalaCards|HPO C2107732 Consistent heat intolerance C0265331 Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) MalaCards C0751295 Memory loss or impairment C0220669 Familial benign neonatal epilepsy MalaCards|HPO C0424755 Fever symptoms C0013289 Duodenal diseases HSDN C0018991 Paralysis one side of body C0021603 Sleep initiation and maintenance disorders HSDN C0426636 Rectal urgency C1335686 Neuroendocrine neoplasm of rectum MalaCards C0344435 Ventricular fibrillation by ecg finding C3150943 Long qt syndrome 2 MalaCards|HPO C0036572 Convulsion C1333760 Gasserian ganglion meningioma UMLS C0030193 Sense of pain C0338473 Neuroaxonal dystrophies HSDN C1963170 Hypothermia adverse event C0001883 Airway obstruction HSDN C0042963 Symptoms vomiting C0023055 Laryngeal neoplasm HSDN C4084768 Usual severity vomiting C0600041 Infective cystitis HSDN C3541349 Syncope C0027643 Neoplasm recurrence, local HSDN C4084769 Vomiting frequency C0024530 Malaria HSDN C1962972 Proteinuria adverse event C0004935 Animal ethology HSDN C0557874 Global developmental delay C3554609 Mental retardation, autosomal recessive 35 MalaCards C0151786 Weakness muscle C0684743 Malignant neoplasm of muscle HSDN C3463815 Feel fatigue C0018188 Granuloma HSDN C0026826 High muscle tone C0014670 Equinus contracture HSDN C0002962 Angina C0009373 Colonic diseases HSDN C2911647 Weight gain adverse event C0006114 Cerebral edema HSDN C0015672 Decreased energy C3539923 Cdisc adas-cog - orientation summary score HSDN C0040264 Ear ringing sound C0062527 Hepatitis b vaccine HSDN C0043094 Weight gain C0029396 Heterotopic ossification HSDN C0010520 Skin cyanosis C0272104 Stokvis UMLS C0015230 Exanthem C0276286 Onyong-nyong fever MalaCards C0018991 Paralysis one side of body C0344434 Atrial fibrillation ecg HSDN C0241137 Skin pallor C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C4049644 Depression C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C2096293 Ent surgical result ear vertigo C0376527 Neoplasm, skull base HSDN C0518090 Frequency of pain question C3808991 Congenital disorder of deglycosylation MalaCards C0040822 D tremors C0024586 Malignant carcinoid syndrome HSDN C0009421 Comatose C0242342 Sheehan syndrome MalaCards C0018965 Blood urine C0011644 Scleroderma MalaCards C4084766 Vomiting C0268568 Classic maple syrup urine disease HPO C0003469 Anxiety disorder C0022134 Islet cell adenoma MalaCards C0424755 Fever symptoms C0017921 Glycogen storage disease type ii MalaCards|HPO C0004134 Dyssynergia C0024748 Alpha-mannosidosis HSDN C0020538 Hbp C2749485 Nblst1 HPO C0520966 Coordination impaired C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C1963281 Vomiting adverse event C0085278 Antiphospholipid syndrome HSDN C0018681 Headache, cephalalgia C0751587 Cadasil syndrome OrphaNet|HSDN C4084767 Bothered by vomiting C0032914 Pre-eclampsia HSDN C2096293 Ent surgical result ear vertigo C0314657 Genetic predisposition HSDN C0011206 Delirium acute C0037579 Soft tissue neoplasms HSDN C0040034 Thrombocytopenia C1854520 Sebastian syndrome HPO C0024032 Birth weight subnormal C0015625 Fanconi anemia MalaCards|HPO C0013362 Dysarthrias C0086650 Mps iii d HPO C0027066 Myoclonic jerking C0268281 Infantile neuronal ceroid lipofuscinosis OrphaNet|HPO|MalaCards C0030975 Disorders perception C0003469 Anxiety disorders HSDN C4084769 Vomiting frequency C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0036572 Convulsion C0009450 Disease caused by microorganism HSDN C0018681 Headache, cephalalgia C0006277 Bronchitis HSDN C0009792 Consciousness disorder C0032268 Pneumocephalus HSDN C4084726 Distress cough C0262655 Recurrent urinary tract infection HSDN C0007758 Cerebellar ataxia C0268125 Purine-nucleoside phosphorylase deficiency HPO C0011991 Loose stools C0010631 Cystadenocarcinoma HSDN C0151908 Dry skin C0221036 Acrodermatitis enteropathica OrphaNet|HPO C1288081 Inflammatory testicular mass C0029191 Orchitis UMLS C1069915 Vertigo C1263846 Attention deficit hyperactivity disorder HSDN C0007398 Catatonic C0038220 Status epilepticus HSDN C3539895 Pelvic pain occurs with bowel movement C0036864 Sexual relations HSDN C0004604 Pain back C0001807 Aggressive behavior HSDN C0741354 Axillary swelling C2129387 Left axillary swelling UMLS C4084776 Weight loss C0079731 B-cell lymphomas HSDN C3641756 Have diarrhea C0020625 Hyponatremia HSDN C4084767 Bothered by vomiting C0024232 Lymphatic metastasis HSDN C4085222 Nausea C0042594 Vestibular diseases HSDN C4085862 Bothered by nausea C0003175 Anthrax disease MalaCards C0557874 Global developmental delay C0268354 De barsy syndrome HPO C0004604 Pain back C0036202 Sarcoidosis HSDN C1384666 Decreased hearing C0014121 Bacterial endocarditis HSDN C0454644 Delayed language development C0342727 3-@methylglutaconic aciduria, type i OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C1834580 Myoclonus and ataxia MalaCards C3665346 Loss sight C1970840 Leukoencephalopathy with metaphyseal chondrodysplasia MalaCards|UMLS C2237041 Shox gene with short stature C2931093 Osteogenesis imperfecta, type 5 MalaCards C3665347 Vision impaired C0268151 Classical galactosemia MalaCards C3898969 Have been vomiting C0242188 Spider bites HSDN C0009806 Constipate C2350521 Gustatory perception HSDN C0015469 Facial paralysis C1546747 Specimen source codes - polyps HSDN C0015672 Decreased energy C0023467 Leukemia, myelocytic, acute HSDN C0015300 Ocular proptosis C0025284 Meningeal neoplasms MalaCards C0684343 Pseudophakia C0010054 Coronary arteriosclerosis HSDN C0424755 Fever symptoms C0026590 Child mother relationship HSDN C4085211 Pain distress question C0003950 Ascariasis HSDN C1549543 Administration method - pain C0035613 Rift valley fever HSDN C0015230 Exanthem C0263210 Non infectious dermatitis pyoderma faciale UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1963107 Euphoria adverse event HSDN C4042891 Sleep wake disorders C0013504 Echinococcosis, hepatic HSDN C0917801 Sleep disorder insomnia C0033139 Primary insomnia UMLS C0027497 Queasy C4085311 Depression - recess HSDN C4084784 Diarrhea C0340629 Aortic aneurysm without mention of rupture nos HSDN C1000483 Genus anemia C1333088 Colonic hamartomatous polyps MalaCards C4084784 Diarrhea C0037939 Spinal neoplasms HSDN C0085593 Chill C0043541 Zygomycoses HSDN C3887873 Hearing loss C1704972 Genomic orientation HSDN C1963063 Anorexia adverse event C0023904 Liver neoplasms, experimental HSDN C0398650 Idiopathic thrombocytopenia purpura C1842763 Spondyloenchondrodysplasia with immune dysregulation MalaCards|HPO C1145670 Failure respiratory C0546264 Congenital fiber type disproportion HPO C0015230 Exanthem C0040034 Thrombocytopenia UMLS C0009421 Comatose C0012979 Canine disease HSDN C0557874 Global developmental delay C0265268 Adams oliver syndrome HPO C0022346 Yellow skin C0019159 Hepatitis a DiseaseOntology|UMLS|MalaCards C0019079 Bloody sputum C0439840 Reflex motion descriptor HSDN C0037384 Snore C0033975 Psychotic disorders HSDN C0026821 Cramp C4082173 Porencephaly HSDN C0037384 Snore C0003850 Arteriosclerosis HSDN C4084776 Weight loss C0015726 Focused anxiety HSDN C0270777 Cord edema spinal C0037928 Spinal cord diseases UMLS C0040822 D tremors C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0027066 Myoclonic jerking C1846367 Spinocerebellar ataxia 19 HPO C0020455 Hypergammaglobulinemia C0206062 Lung diseases, interstitial HSDN C0011991 Loose stools C0040843 Treponemal disease HSDN C1557397 Adverse event associated with pain C0152814 Epididymal tuberculosis MalaCards C4084769 Vomiting frequency C0033845 Pseudotumor cerebri HSDN C0012833 Dizzy C0019562 Von hippel-lindau syndrome MalaCards|HSDN|HPO C0000737 Abdomen pain C0279610 Wilm's tumor, stromal predominant UMLS C0018991 Paralysis one side of body C0392550 Hemiplegia, infantile UMLS C0242936 Center pain C0011586 Three dimensional vision HSDN C4085661 Usual severity nausea C0751908 Vestibular neuronitis HSDN C0027066 Myoclonic jerking C3538999 Dystonia 23 MalaCards|UMLS C3898969 Have been vomiting C3463824 Myelodysplastic syndrome HSDN C0027498 Nausea vomiting C1739094 Foodborne botulism OrphaNet|MalaCards C0033377 Caudal displacement C0546264 Congenital fiber type disproportion HPO C1963063 Anorexia adverse event C1527429 Increased blood npn HSDN C0234146 Absent reflex C3553354 Coenzyme q10 deficiency, primary, 2 MalaCards C3898969 Have been vomiting C0022658 Kidney diseases HSDN C0036572 Convulsion C3494977 Migrating partial seizures in infancy, intractable UMLS C0020580 Decreased sensation C0009088 Cluster headache HSDN C1557397 Adverse event associated with pain C0037280 Skin diseases, parasitic HSDN C0851578 Disorder sleep C0005686 Urinary bladder diseases HSDN C0020538 Hbp C1527168 Bonnevie-ullrich syndrome MalaCards C0020796 Profoundly mentally retarded C1839332 Rett syndrome, preserved speech variant HPO C4085211 Pain distress question C0016662 Fracture open HSDN C3898969 Have been vomiting C0740392 Infarction, middle cerebral artery HSDN C1856661 Cornea cloudy C1862839 Anterior segment mesenchymal dysgenesis HPO C3887638 Failure to thrive in infant C2931092 Maternally inherited leigh syndrome MalaCards C0850758 Pain pelvic C0042253 Vaginal fistula HSDN C2242996 Tingling C0014457 Eosinophilia HSDN C3641756 Have diarrhea C3661523 Congenital intestinal aganglionosis MalaCards|HPO C4085661 Usual severity nausea C0019069 Hemophilia a HSDN C0031315 Phantom limb pain C0002768 Congenital pain insensitivity HSDN C0004134 Dyssynergia C1706192 Sulfatidosis MalaCards C4042891 Sleep wake disorders C0027809 Neurilemmoma HSDN C3665347 Vision impaired C3887937 Cone dystrophy 5, x-linked MalaCards C0013362 Dysarthrias C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0004134 Dyssynergia C0376527 Neoplasm, skull base HSDN C0015230 Exanthem C0549660 Other skin disorders UMLS C0030193 Sense of pain C2117329 X-ray of toe: polydactyly HSDN C0013421 Dystonia C1832466 Capos syndrome HPO C3887638 Failure to thrive in infant C0268647 Lysinuric protein intolerance MalaCards|HPO C0042963 Symptoms vomiting C0001584 Adolescent psychology HSDN C0413252 Hypothermia due to exposure C1578691 Congenital myxedema MalaCards C0033774 Skin pruritus C0346210 Vulval intraepithelial neoplasia UMLS C1549543 Administration method - pain C1145628 Autonomic nervous system disorders HSDN C4085222 Nausea C1546635 Specimen source codes - fistula HSDN C1963252 Tremor adverse event C0024535 Malaria, falciparum HSDN C4085862 Bothered by nausea C0011615 Dermatitis, atopic HSDN C3539892 Pelvic pain in front C0008519 Ectopic tissue HSDN C0013132 Drooling C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0034067 Pulmonary emphysema HSDN C1279888 Proteinuria of undiagnosed cause C2674045 Urogenital adysplasia HPO C1549543 Administration method - pain C0014145 Yolk sac tumor HSDN C4084776 Weight loss C1261473 Sarcoma HSDN C3163620 Hypotension adverse event C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0152169 Colic renal C1704212 Embolism embolus HSDN C0497406 Over weight C0018213 Graves disease HSDN C4084766 Vomiting C1563706 Nephrogenic diabetes insipidus, type ii HPO C4084768 Usual severity vomiting C1283620 Sucrase-isomaltase deficiency, congenital OrphaNet|MalaCards C2984058 Have pain C0020461 Hyperkalemia HSDN C0013456 Pain ear C0010606 Adenoid cystic carcinoma HSDN C0149651 Clubbing C1868081 Juvenile polyposis coli HPO C0520909 Ponv C0038356 Stomach neoplasms HSDN C0162429 Dietary deficiency C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0009421 Comatose C0039128 Syphilis HSDN C0013362 Dysarthrias C1851708 Encephalopathy, recurrent, of childhood MalaCards C0155552 Hearing loss mixed C1864323 Orofacial cleft 2 MalaCards C0042928 Paralysis vocal cord C0002792 Anaphylaxis HSDN C0042025 Urinary incontinence stress C0004275 Attitude health HSDN C0344306 Intercostal neuralgia C0039978 Thoracic diseases UMLS C0085631 Abnormal excitement C0009450 Disease caused by microorganism HSDN C4085317 Diarrhea frequency C0020502 Hyperparathyroidism HSDN C2984058 Have pain C0005690 Bladder fistula HSDN C1384666 Decreased hearing C0282527 Infantile refsum disease (disorder) OrphaNet|MalaCards C0518090 Frequency of pain question C0005424 Biliary tract diseases HSDN C3539020 Pelvic pain decreasing in frequency C0037369 Smoking HSDN C0020580 Decreased sensation C0029340 Orthomolecular therapy HSDN C0850149 Cough dry C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C2984058 Have pain C0023220 Leg injury HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0007762 Cerebellar neoplasms HSDN C4085210 Usual severity pain C0220981 Metabolic acidosis HSDN C0030193 Sense of pain C1335502 Adenoid cystic carcinoma of prostate UMLS C1557397 Adverse event associated with pain C0041974 Urethral stricture HSDN C0027066 Myoclonic jerking C0026975 Myelitis HSDN C0000737 Abdomen pain C3897535 Stage iic rectal cancer UMLS C4084802 Usual severity diarrhea C1864996 Enteric neuropathy, familial MalaCards C1549543 Administration method - pain C0206663 Neuroectodermal tumor, primitive HSDN C0015672 Decreased energy C0007117 Basal cell carcinoma HSDN C0241165 Skin thickening C2931828 Keratoderma and spastic paralysis MalaCards C1963091 Diarrhea adverse event C0853697 Neutrophil count decreased HSDN C4084784 Diarrhea C0017563 Gingival diseases HSDN C0162298 Stiffness joints C0265514 Dermatofibrosis lenticularis disseminata OrphaNet|UMLS|HPO|MalaCards C0015672 Decreased energy C0009435 Commitment of mentally ill HSDN C0018834 Brash C4014708 Hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies MalaCards C4085862 Bothered by nausea C0042961 Intestinal volvulus HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020523 Immediate hypersensitivity HSDN C0004604 Pain back C0042830 Perception visual HSDN C1963170 Hypothermia adverse event C0750394 Wbc low HSDN C1384666 Decreased hearing C0038525 Subarachnoid hemorrhage HSDN C3463815 Feel fatigue C0032249 Plummer vinson syndrome HSDN C0152169 Colic renal C0034183 Pyelitis unspecified HSDN C0027497 Queasy C0021400 Influenza HSDN C0026838 Spasticity muscle C0023521 Globoid cell leukodystrophy OrphaNet C3898969 Have been vomiting C0997768 Glaucoma HSDN C1963281 Vomiting adverse event C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C2219953 Middle-night awakening and having a cigarette C0393761 Fitful sleep UMLS C2936821 Spinal cerebrospinal fluid leak C0032269 Pneumococcal infections HSDN C0030554 Abnormal sensation C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0241165 Skin thickening C3665732 Metastatic dermatofibrosarcoma protuberans MalaCards C0013404 Respiratory difficulty C0001815 Primary myelofibrosis HSDN C0042963 Symptoms vomiting C0014854 Esophageal diverticulum HSDN C4085210 Usual severity pain C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C4085661 Usual severity nausea C0042514 Tachycardia, ventricular HSDN C1384666 Decreased hearing C0270724 Infantile neuroaxonal dystrophy HPO C0042571 Vertigo subjective C0025284 Meningeal neoplasms HSDN C4084775 Usual severity weight loss C0007124 Noninfiltrating intraductal carcinoma HSDN C0008031 Pain chest C0042035 Urination disorders HSDN C0018524 Hallucinate C0011882 Diabetic neuropathies HSDN C0015672 Decreased energy C0019069 Hemophilia a HSDN C4085211 Pain distress question C0085298 Sudden cardiac death HSDN C3829611 Nausea frequency C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C1963065 Apnea adverse event C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal HPO C1549543 Administration method - pain C0020757 Ichthyoses HSDN C0018772 Deafness C0025472 Mesenteric vascular occlusion HSDN C0086565 Liver function abnormal C0751202 Cystathionine beta-synthase deficiency disease HPO C0019209 Large liver C1843355 Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0206663 Neuroectodermal tumor, primitive MalaCards C0007758 Cerebellar ataxia C0023264 Leigh disease OrphaNet|HPO|MalaCards C0020580 Decreased sensation C3711850 Opticospinal multiple sclerosis MalaCards C2911645 Weight loss adverse event C0008924 Cleft lip HSDN C2984058 Have pain C0040028 Thrombocythemia, essential HSDN C0231835 Respiration rate increased C0242488 Acute lung injury HSDN C0235153 Sensory hallucination C1855369 Maple syrup urine disease, type ia HPO C2024878 Cardiovascular surgery result: dyspnea C0850803 Anaphylaxis (non medication) HSDN C1963281 Vomiting adverse event C0033906 Psychological theories HSDN C4084776 Weight loss C0001418 Adenocarcinoma HSDN C4085211 Pain distress question C0004576 Babesiosis HSDN C3539889 Pelvic pain increasing in severity C0042996 Vulvitis unspecified HSDN C0004941 Behavioral symptoms C0002986 Fabry disease OrphaNet C2203646 Jaundice C0717360 Disease lyme vaccine HSDN C0237849 Skin desquamation C1853354 Peeling skin syndrome, acral type OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0262584 Carcinoma, small cell HSDN C4084767 Bothered by vomiting C0015401 Foreign body in eye HSDN C0004604 Pain back C0004238 Atrial fibrillation HSDN C0036572 Convulsion C0206255 Malaria vaccine HSDN C0004604 Pain back C0302148 Blood clot HSDN C0423823 Nail thinness C0795830 Chromosome 9p deletion syndrome OrphaNet|MalaCards C0034933 Abnormal reflexes C0007930 Chagas cardiomyopathy HSDN C0221170 Stiffness muscle C3714934 Myopathy, myofibrillar, 3 MalaCards C2919142 Short stature adverse event C2931183 Faces syndrome OrphaNet|MalaCards C4085862 Bothered by nausea C0948039 Bacterial gastritis MalaCards C0005745 Blepharoptosis C0796033 Marden-walker syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0242698 Ventricular dysfunction, left HSDN C0041105 Jaw spasm C0026633 Mouth abnormalities HSDN C0751295 Memory loss or impairment C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C0497247 Blood pressure elevation C3887949 Apparent mineralocorticoid excess MalaCards C1962972 Proteinuria adverse event C0034088 Pulmonary valve insufficiency HSDN C0017181 Gastrointestinal bleed C2931916 Midline granulomatosis MalaCards C1963087 Constipation adverse event C1261473 Sarcoma HSDN C0003550 Broca aphasia C0004377 Automatism HSDN C0020538 Hbp C1619700 Renal adysplasia MalaCards|HPO C0041657 Consciousness loss C0007786 Brain ischemia HSDN C0009676 Confusion state C0041755 Adverse reaction to drug HSDN C4084766 Vomiting C0017563 Gingival diseases HSDN C0003910 Articulation disorder C0017510 Gestures HSDN C2242996 Tingling C0022134 Islet cell adenoma MalaCards C4085549 Dizziness C0024236 Lymphedema HSDN C0013604 Edematous C0002453 Amenorrhea HSDN C0002965 Crescendo angina C0036202 Sarcoidosis HSDN C0162834 Hyperpigmentation C1850568 Nakajo syndrome MalaCards|HPO C1963091 Diarrhea adverse event C0085092 Parenting behavior HSDN C0011991 Loose stools C3714580 Hypokalemic periodic paralysis type 1 HSDN C1963237 Insomnia adverse event C0175702 Williams syndrome OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0026650 Movement disorders HSDN C3463815 Feel fatigue C0004106 Astigmatism HSDN C0001327 Laryngitis acute C0085860 Autoimmune syndrome type ii, polyglandular MalaCards C0030552 Paralysis partial C0520720 Cyst nerve root MalaCards C0018681 Headache, cephalalgia C1332285 Anaplastic (malignant) intracranial meningioma UMLS C2315100 Pediatric failure to thrive C1838457 Fanconi anemia, complementation group d1 HPO C0032617 High urine output C0039231 Tachycardia HSDN C0917816 Deficiency mental C3151140 Pontocerebellar hypoplasia, type 2d MalaCards C0027066 Myoclonic jerking C0009952 Febrile convulsions HSDN C4084776 Weight loss C0027626 Neoplasm invasiveness HSDN C4085222 Nausea C0152724 Tuberculosis of intestines and mesenteric glands DiseaseOntology|MalaCards C2315100 Pediatric failure to thrive C0152094 Cellular immunodeficiency with abnormal immunoglobulin deficiency MalaCards C0332573 Macula C0080024 Piebaldism OrphaNet|HPO C0003862 Pain joint C0034628 Radius fracture HSDN C0027796 Neuralgias C1861329 Spinal canal stenosis HSDN C0010200 Cough symptom C0004623 Bacterial infections HSDN C0034151 Hyperglobulinemic purpura C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C1549543 Administration method - pain C0005690 Bladder fistula HSDN C3539895 Pelvic pain occurs with bowel movement C1963088 Cystitis adverse event HSDN C0015676 Mental fatigue C0011551 Depersonalisation HSDN C0349506 Sun sensitivity C1866504 Photosensitive trichothiodystrophy MalaCards|HPO C0040264 Ear ringing sound C0010068 Coronary heart disease HSDN C2984058 Have pain C0020876 Ileal neoplasms HSDN C0025287 Meningitis-like C0041466 Typhoid fever HSDN C1963281 Vomiting adverse event C0020445 Hypercholesterolemia, familial HSDN C2911645 Weight loss adverse event C1522137 Hypertriglyceridemia result HSDN C3898969 Have been vomiting C1527348 Brain hypoxia HSDN C4085642 Level of joint stiffness C3146244 Alcohol related birth defect OrphaNet|MalaCards C0030193 Sense of pain C0393745 Chronic post-traumatic headache UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0001828 Agricultural workers' diseases HSDN C0151889 Reflexes tendon increased C0751435 Hyperphenylalaninaemia MalaCards C0851578 Disorder sleep C3163620 Hypotension adverse event HSDN C4084724 Usual severity constipation C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C0151889 Reflexes tendon increased C0270726 Alexander disease OrphaNet|MalaCards C0036572 Convulsion C0524851 Neurodegenerative disorders HSDN C0917816 Deficiency mental C0339527 Leber congenital amaurosis MalaCards|HPO C0018784 Deafness sensorineural C0007873 Uterine cervical neoplasm HSDN C0241210 Speaking delay C2930913 Chromosome 13q deletion MalaCards C0020673 Hypothermia (central) (local) C0700327 Clinical findings relating to memory HSDN C0206160 Retic count elevated C0001621 Adrenal gland diseases HSDN C0018681 Headache, cephalalgia C3899666 Childhood ependymoblastoma UMLS C0522224 Palsied C2984302 Leishmaniasis infection pathway HSDN C2315100 Pediatric failure to thrive C0014850 Esophageal atresia HSDN C3887638 Failure to thrive in infant C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C0020673 Hypothermia (central) (local) C0010674 Cystic fibrosis HSDN C1963184 Nystagmus adverse event C0344559 Irido-corneo-trabecular dysgenesis (disorder) HPO C3829611 Nausea frequency C0021603 Sleep initiation and maintenance disorders HSDN C1557397 Adverse event associated with pain C0036429 Sclerosis HSDN C0030552 Paralysis partial C0036357 Psychology, schizophrenic HSDN C1963167 Memory impairment adverse event C1853554 Radiation induced meningioma MalaCards C1963170 Hypothermia adverse event C0024305 Lymphoma, non-hodgkin HSDN C4084774 Have weight loss C0042164 Uveitis HSDN C0042755 Virilisation C0027577 Nelson syndrome HSDN C2237041 Shox gene with short stature C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C0036572 Convulsion C0003537 Aphasia MalaCards C2024878 Cardiovascular surgery result: dyspnea C0024225 Inflammation lymphatic HSDN C4084802 Usual severity diarrhea C0037928 Spinal cord diseases HSDN C3665347 Vision impaired C1845446 Corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia HPO C0042798 Vision dim C0410174 Fukuyama type congenital muscular dystrophy MalaCards|HPO C0018681 Headache, cephalalgia C2931842 Diaphyseal dysplasia 1, progressive MalaCards|HPO C0037316 Not enough sleeping C0004161 Athletic injuries HSDN C0009676 Confusion state C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C1963091 Diarrhea adverse event C0019360 Herpes zoster disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0023473 Myeloid leukemia, chronic HSDN C1856661 Cornea cloudy C0033800 Pseudoglioma MalaCards C4085862 Bothered by nausea C1299919 Enteric coccidiosis HSDN C4085317 Diarrhea frequency C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0009806 Constipate C0018378 Guillain-barre syndrome HSDN C3539020 Pelvic pain decreasing in frequency C0033578 Prostatic neoplasms HSDN C3463815 Feel fatigue C0006384 Bundle-branch block HSDN C0344315 Mood depressed C0339534 Usher syndrome type 2 MalaCards|HPO C0349588 Stature short C0406740 Kohlschutter tonz syndrome MalaCards|HPO C0018780 Frequencies hearing high loss C1832379 Deafness, autosomal dominant 7 (disorder) MalaCards C0522224 Palsied C0005591 Avian disease HSDN C3539891 Pelvic pain to the rear C0037313 Sleep HSDN C0413252 Hypothermia due to exposure C0002895 Anemia, sickle cell HSDN C0522224 Palsied C0004352 Autistic disorder HSDN C0040822 D tremors C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0006114 Cerebral edema HSDN C0013395 Indigestion C0086543 Cataract nos HSDN C0004134 Dyssynergia C0037773 Spastic paraplegia, hereditary OrphaNet|HSDN|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0600041 Infective cystitis HSDN C0149793 Transient monocular blindness C0033845 Pseudotumor cerebri HSDN C0025287 Meningitis-like C0042338 Herpesvirus 3, human HSDN C4084788 Have dizziness C1963119 Stomach ulcer adverse event HSDN C0085636 Light sensitivity C0000880 Acanthamoeba keratitis OrphaNet|MalaCards C3539892 Pelvic pain in front C0030455 Parametritis HSDN C0003862 Pain joint C2984299 Asthma pathway HSDN C4085549 Dizziness C0699744 Infection of ear HSDN C0015970 Fever unknown origin C0314657 Genetic predisposition HSDN C0030552 Paralysis partial C0032269 Pneumococcal infections HSDN C0013404 Respiratory difficulty C0007193 Cardiomyopathy, dilated UMLS C0851578 Disorder sleep C0237873 Physiological sexual disorders HSDN C0027497 Queasy C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C0013428 Painful urination C1332563 Bladder signet ring cell adenocarcinoma UMLS C4084802 Usual severity diarrhea C0001430 Adenoma HSDN C0728710 Pupil constriction observed C0016236 Flicker fusion HSDN C1963281 Vomiting adverse event C0017185 Gastrointestinal neoplasms HSDN C0155552 Hearing loss mixed C0026703 Mucopolysaccharidoses HSDN C0042798 Vision dim C0002395 Alzheimer's disease HSDN C0018784 Deafness sensorineural C1859774 Optic nerve hypoplasia and abnormalities of the central nervous system HPO C3641755 Have constipation C0042138 Uterine neoplasms HSDN C0018991 Paralysis one side of body C0038661 Suicide HSDN C0000737 Abdomen pain C1709507 Peritoneal well differentiated papillary mesothelioma UMLS C0024031 Back pain lower back C0242350 Erectile dysfunction HSDN C0086437 Joint hypermobility C4225351 White-sutton syndrome UMLS C0003126 Smell loss C0154725 Oth disorder nervous system UMLS C3641756 Have diarrhea C0024638 Class ii division 2 malocclusion HSDN C0004134 Dyssynergia C0268525 5-oxoprolinase deficiency MalaCards C3539022 Pelvic pain decreasing in severity C0017181 Gastrointestinal hemorrhage HSDN C0242936 Center pain C0036285 Scarlet fever HSDN C0022346 Yellow skin C3244301 Coverage level - family HSDN C2984058 Have pain C1527336 Sjogren's syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0001206 Acromegaly HSDN C4042891 Sleep wake disorders C0024115 Lung diseases HSDN C0454644 Delayed language development C1864923 Northern epilepsy syndrome MalaCards C0232466 Feeding difficulty C2940785 Hypothyroidism, congenital, nongoitrous, 3 MalaCards C0013404 Respiratory difficulty C0001430 Adenoma HSDN C0015300 Ocular proptosis C0432242 Desbuquois syndrome OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C1832817 Klippel-feil deformity, conductive deafness, and absent vagina MalaCards C0033774 Skin pruritus C0570513 Acetaminophen allergy UMLS C4085317 Diarrhea frequency C1546533 Specimen source codes - abscess HSDN C0004134 Dyssynergia C0026975 Myelitis HSDN C1962972 Proteinuria adverse event C3810100 Fanconi renotubular syndrome 3 MalaCards C0026838 Spasticity muscle C0022758 Kap HSDN C0018834 Brash C0041296 Tuberculosis HSDN C0034155 Thrombotic thrombocytopenic purpura C0009375 Colonic neoplasms HSDN C2919142 Short stature adverse event C3151120 Meier-gorlin syndrome 4 MalaCards C2203646 Jaundice C0018802 Congestive heart failure HSDN C0600142 Flash hot C0001418 Adenocarcinoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0030305 Pancreatitis HSDN C1963071 Back pain adverse event C3887650 Adult rickets HSDN C1384666 Decreased hearing C0036357 Psychology, schizophrenic HSDN C1069915 Vertigo C0011265 Presenile dementia HSDN C0151786 Weakness muscle C0812437 Oculo-dento-digital syndrome OrphaNet|HPO|MalaCards C3887638 Failure to thrive in infant C0037268 Skin abnormalities HSDN C4084776 Weight loss C0040185 Tibia fracture HSDN C0518090 Frequency of pain question C2827407 Infectious otitis media HSDN C2203646 Jaundice C0026769 Multiple sclerosis HSDN C2237041 Shox gene with short stature C3714796 Isolated somatotropin deficiency MalaCards C1557397 Adverse event associated with pain C0030297 Pancreatic neoplasm HSDN C0036572 Convulsion C0265287 Acromicric dysplasia HPO C4084775 Usual severity weight loss C1527336 Sjogren's syndrome HSDN C0030193 Sense of pain C0013502 Echinococcosis HSDN C0015230 Exanthem C0406329 Psoriasis palmaris UMLS C0241057 Skin burning sensation C0343068 Familial cold urticaria OrphaNet|HPO|MalaCards C0018772 Deafness C0020461 Hyperkalemia HSDN C0039870 Leanness C0040053 Thrombosis HSDN C0522224 Palsied C0281865 Hip injury HSDN C2911645 Weight loss adverse event C0345904 Malignant neoplasm of liver MalaCards C0026603 Motion sickness C0018802 Congestive heart failure HSDN C1384666 Decreased hearing C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C0040034 Thrombocytopenia C1856447 Bernard soulier syndrome, type b HPO C4042891 Sleep wake disorders C1962979 Burn adverse event HSDN C0557874 Global developmental delay C3151069 Chromosome 17p13.1 deletion syndrome MalaCards C2187990 Unable to perform sex C0022972 Lambert-eaton myasthenic syndrome MalaCards C0424755 Fever symptoms C0002390 Extrinsic allergic alveolitis HSDN C0018772 Deafness C1567744 Alport syndrome, autosomal recessive MalaCards|HPO C1963167 Memory impairment adverse event C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C0162298 Stiffness joints C3711158 Metatropic dwarfism, type ii MalaCards C0034150 Skin purpura C0270611 Brain damage HSDN C3829611 Nausea frequency C0019196 Hepatitis c DiseaseOntology|HSDN|MalaCards C0009421 Comatose C0025294 Meningococcal meningitis HSDN C4085211 Pain distress question C0497552 Congenital neurologic anomalies HSDN C0086439 Activity decreased C1836797 Combined oxidative phosphorylation deficiency 1 MalaCards|HPO C0030232 Color loss C0272118 Warm autoimmune hemolytic anemia OrphaNet|MalaCards C0013362 Dysarthrias C0162309 Adrenoleukodystrophy HSDN C0848203 Male pelvic pain C0010692 Cystitis HSDN C0522224 Palsied C0031347 Pharyngeal neoplasms HSDN C0424755 Fever symptoms C0007642 Cellulitis nos HSDN C0018991 Paralysis one side of body C0026771 Trauma multiple HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0032969 Pregnancy in diabetics HSDN C0030193 Sense of pain C2004491 Cicatrix HSDN C0000727 Abdomen acute C0029408 Degenerative polyarthritis HSDN C1962972 Proteinuria adverse event C0018801 Heart failure HSDN C4085862 Bothered by nausea C0032708 Disorders of porphyrin metabolism HSDN C0264588 Dysphonia spasmodic C3281236 Dystonia 21 MalaCards C4084723 Constipation C0002895 Anemia, sickle cell HSDN C4084724 Usual severity constipation C0019069 Hemophilia a HSDN C0020673 Hypothermia (central) (local) C0233629 Thinking and speaking disturbances HSDN C2984058 Have pain C0305062 Tetanus toxoids HSDN C1963086 Confusion adverse event C1306856 Megaloblastic anemia due to inborn errors of metabolism HPO C0013378 Dysgensia C0024689 Mandibular diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242596 Neoplasm, residual HSDN C4085211 Pain distress question C1527348 Brain hypoxia HSDN C1963090 Dehydration adverse event C1881600 Malignant vipoma MalaCards C0018772 Deafness C0003869 Arthritis, infectious HSDN C0027497 Queasy C1332251 Ampulla of vater squamous cell carcinoma UMLS C2237041 Shox gene with short stature C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0011168 Disorder deglutition C0520719 Spinopontine atrophy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C1546602 Specimen source codes - diverticulum HSDN C0018681 Headache, cephalalgia C1843330 Osteopetrosis, autosomal dominant 1 MalaCards|HPO|UMLS C0019825 Voice hoarseness C0030567 Parkinson disease HSDN C0000737 Abdomen pain C1145670 Respiratory failure HSDN C0018772 Deafness C0023944 Cerebromedullospinal disconnection MalaCards C0032617 High urine output C1579931 Depressed - symptom HSDN C0000737 Abdomen pain C0019100 Severe dengue OrphaNet C4085210 Usual severity pain C0009862 Contraception behavior HSDN C1963087 Constipation adverse event C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C4084768 Usual severity vomiting C0020544 Renal hypertension HSDN C0030552 Paralysis partial C0035358 Retroperitoneal neoplasm HSDN C0030193 Sense of pain C0037268 Skin abnormalities HSDN C4042891 Sleep wake disorders C0525042 Feeding and eating disorders of childhood HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024141 Lupus erythematosus, systemic HSDN C4084784 Diarrhea C0017205 Gaucher disease HSDN C0030193 Sense of pain C0242550 Behavior, risk reduction HSDN C4084768 Usual severity vomiting C2137063 Ent surgical result - speech HSDN C3539896 Pelvic pain occurs with urination C0017638 Glioma HSDN C4085317 Diarrhea frequency C0006075 Bovine virus diarrhea mucosal disease HSDN C2911647 Weight gain adverse event C0034012 Delayed puberty HSDN C2315100 Pediatric failure to thrive C0019096 Hemorrhagic fever, american HSDN C0017181 Gastrointestinal bleed C0376300 Dengue shock syndrome MalaCards C0019209 Large liver C0018203 Chronic granulomatous disease OrphaNet|HPO|MalaCards C1519353 Skin eruption papular C0221011 Malignant atrophic papulosis MalaCards C1999266 Depression adverse event C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0036572 Convulsion C0041328 Renal tuberculosis HSDN C4042891 Sleep wake disorders C0014121 Bacterial endocarditis HSDN C0042928 Paralysis vocal cord C0006434 Burn injury HSDN C0030200 Intractable pain C0009404 Colorectal neoplasms HSDN C4084727 Cough frequency C0041466 Typhoid fever MalaCards C0231791 In toe C1862472 Oculomelic amyoplasia MalaCards C3829611 Nausea frequency C0011609 Drug eruptions HSDN C3539891 Pelvic pain to the rear C0010695 Cystocele HSDN C0557874 Global developmental delay C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0030849 Penile neoplasms HSDN C0086565 Liver function abnormal C2752007 Congenital disorder of glycosylation, type io MalaCards|HPO C0033774 Skin pruritus C1335299 Pancreatic adenosquamous carcinoma UMLS C3539896 Pelvic pain occurs with urination C0001442 Adenosarcoma HSDN C2984058 Have pain C0019034 Hemoglobin sc disease MalaCards|HSDN C2024893 Cardiovascular surgery result: fatigue C0020676 Hypothyroidism HSDN C0426579 Anorexia symptom C0040809 Patient refusal of treatment HSDN C4084784 Diarrhea C0019054 Hemolysis (disorder) HSDN C1963091 Diarrhea adverse event C0039231 Tachycardia HSDN C4084776 Weight loss C0027126 Myotonic dystrophy HSDN C0234376 Tremor action C1864663 Hypomyelination and congenital cataract MalaCards|UMLS C0019209 Large liver C1847720 Glycine n-methyltransferase deficiency MalaCards|HPO C0812426 Kidney problem C0746832 Nephritis interstitial allergic UMLS C0003862 Pain joint C0001144 Acne vulgaris HSDN C2024893 Cardiovascular surgery result: fatigue C0029883 Otitis media with effusion HSDN C0036572 Convulsion C0338503 Septo-optic dysplasia OrphaNet|HSDN|HPO C4085548 Usual severity dizziness C0752322 Epilepsy, partial, sensory HSDN C0018772 Deafness C0041227 Trypanosomiasis HSDN C0026821 Cramp C0012746 Dissociative disorder HSDN C1145670 Failure respiratory C0340427 Familial dilated cardiomyopathy MalaCards C0242936 Center pain C0026918 Mycobacterium infections HSDN C0020505 Excessive eating C0024141 Lupus erythematosus, systemic HSDN C0020450 Hyperemesis gravidarum C0004096 Asthma HSDN C0221752 Rbc urine C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C0242936 Center pain C0001584 Adolescent psychology HSDN C0428977 Pulse rate decrease C2939462 Immunoglobulin deposition disease MalaCards C0022346 Yellow skin C0023817 Hyperlipoproteinemia type i HPO C4084784 Diarrhea C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C1384666 Decreased hearing C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C3494358 Characteristic, prodromal C0027902 Neuropsychological diagnosis HSDN C0151786 Weakness muscle C3814778 Hemolytic index HSDN C4084725 Usual severity cough C0036974 Shock HSDN C2242996 Tingling C0024693 Mandible injury HSDN C1549543 Administration method - pain C1720887 Female urogenital diseases HSDN C0035229 Respiratory function impaired C0344679 Atresia; pulmonary vein OrphaNet|MalaCards C1963065 Apnea adverse event C0015745 Ingestive behavior HSDN C0015469 Facial paralysis C1850569 Nemaline myopathy 2 HPO C0036572 Convulsion C0016663 Pathological fracture HSDN C0038990 Sweats C3808991 Congenital disorder of deglycosylation MalaCards C0037316 Not enough sleeping C0033968 Psychotherapeutic technique HSDN C0022107 Fussiness C0751291 Desmoplastic medulloblastoma MalaCards C2096293 Ent surgical result ear vertigo C0003864 Arthritis HSDN C0018681 Headache, cephalalgia C0018805 Heart injuries HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036986 Shock, traumatic HSDN C0000737 Abdomen pain C2981399 Stage iib colorectal cancer UMLS C4084769 Vomiting frequency C0155866 Inhalational anthrax OrphaNet|MalaCards C0027498 Nausea vomiting C0744297 Gastric outlet obstruction partial UMLS C3539890 Pelvic pain causes awakening at night C0033348 Language program HSDN C0020505 Excessive eating C0520716 Pallidopontonigral degeneration HPO C3887638 Failure to thrive in infant C2931008 Congenital disorder of glycosylation type 2a MalaCards|HPO C1069915 Vertigo C0039590 Testicular neoplasms HSDN C0427068 Legs weakness C1846685 Spastic paraplegia 19, autosomal dominant (disorder) MalaCards C0030193 Sense of pain C0242216 Biliary calculi HSDN C0575081 Abnormal gait C1851481 Erythrokeratodermia with ataxia OrphaNet|HPO C0151786 Weakness muscle C0752235 Lyme neuroborreliosis MalaCards C2024893 Cardiovascular surgery result: fatigue C0233610 Negativism in catatonia HSDN C0013456 Pain ear C0393735 Headache disorders UMLS C0007859 Pain neck C0751955 Brain infarction HSDN C0518090 Frequency of pain question C0011432 Dentin hypersensitivity HSDN C4042891 Sleep wake disorders C0023418 Leukemia HSDN C4085211 Pain distress question C1449861 Micronuclei, chromosome-defective HSDN C0042963 Symptoms vomiting C0338437 Neurocysticercosis HSDN C1549543 Administration method - pain C0038940 Surgical wound dehiscence HSDN C3815497 Cough C0011127 Pressure ulcer HSDN C0026826 High muscle tone C1848144 Woods black norbury syndrome MalaCards C0018926 Emesis bloody C3489413 Lipomatosis, multiple HSDN C4085210 Usual severity pain C0029944 Drug overdose HSDN C3641756 Have diarrhea C0021400 Influenza HSDN C4085549 Dizziness C0034067 Pulmonary emphysema HSDN C2203646 Jaundice C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0036572 Convulsion C0268225 Aspartylglucosaminuria MalaCards|HPO C0040822 D tremors C0919267 Ovarian neoplasm HSDN C1557397 Adverse event associated with pain C0031350 Pharyngitis HSDN C0030193 Sense of pain C0033893 Tension headache UMLS C2203646 Jaundice C0001824 Agranulocytosis HSDN C4084776 Weight loss C0016542 Foreign body HSDN C0040034 Thrombocytopenia C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C4084726 Distress cough C0020523 Immediate hypersensitivity HSDN C1279888 Proteinuria of undiagnosed cause C0034531 Experimental radiation injuries HSDN C3274924 Have been coughing C0742343 Acute chest syndrome DiseaseOntology|HSDN|MalaCards C0009806 Constipate C0035222 Respiratory distress syndrome, adult HSDN C1549543 Administration method - pain C0002895 Anemia, sickle cell OrphaNet|MalaCards C4084768 Usual severity vomiting C1705812 Nci thesaurus role HSDN C0740418 Back pain chronic C0748678 Shoulder pain chronic UMLS C0000731 Abdomen distention C1856159 Urioste martinez-frias syndrome MalaCards C2029884 Hearing loss by exam C2984572 Malaria pathway HSDN C0022346 Yellow skin C0018801 Heart failure HSDN C1145670 Failure respiratory C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C4084776 Weight loss C0020649 Hypotension HSDN C1557397 Adverse event associated with pain C0282612 Prostatic intraepithelial neoplasias HSDN C2364111 Gustatory anesthesia C0037036 Sialorrhea HSDN C2911645 Weight loss adverse event C0010709 Cyst HSDN C0521172 Eschar C3532354 Far eastern spotted fever MalaCards C1963071 Back pain adverse event C1299262 Sarcoma - category (morphologic abnormality) HSDN C0233514 Behavior abnormal C1864923 Northern epilepsy syndrome OrphaNet|MalaCards C0002962 Angina C0031099 Periodontitis HSDN C4085210 Usual severity pain C0006818 Campylobacter infection HSDN C0011991 Loose stools C0018965 Hematuria HSDN C3665347 Vision impaired C0015625 Fanconi anemia MalaCards|HPO C0235153 Sensory hallucination C0751276 Metachromatic leukodystrophy, juvenile type HPO C0023530 Leukopenia C3151785 Anemia, x-linked, without thrombocytopenia HPO C0042798 Vision dim C0020659 Hypothalamic neoplasms HSDN C1827547 Repetitive behavior C3279716 Hypoacetylaspartia MalaCards C4085317 Diarrhea frequency C0041234 Chagas disease OrphaNet|MalaCards C0018834 Brash C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C3509788 Neonatal jaundice due to excessive hemolysis C0495431 Neonatal jaundice due to polycythaemia UMLS C0008031 Pain chest C0042138 Uterine neoplasms HSDN C0030554 Abnormal sensation C1704421 Skin pigmentation disorder HSDN C0033774 Skin pruritus C0406299 Chronic prurigo UMLS C0037763 Spasm C0155877 Allergic asthma UMLS C0497247 Blood pressure elevation C0403443 Renal failure, progressive, with hypertension MalaCards C0015672 Decreased energy C0034365 Q-sort HSDN C0233514 Behavior abnormal C0020074 Hsan type iv OrphaNet|MalaCards C0234533 Seizure generalized C0206307 Canavan disease MalaCards|HPO C0013404 Respiratory difficulty C1859726 Arterial tortuosity syndrome MalaCards C0042940 Disorder of voice C0006437 Burn, inhalation HSDN C2242996 Tingling C3150972 Neuropathy, hereditary sensory, type id MalaCards|HPO C0008031 Pain chest C0022650 Kidney calculi HSDN C4084776 Weight loss C1963211 Pericarditis adverse event HSDN C0018681 Headache, cephalalgia C0265321 Wyburn-mason syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0035369 Retroviridae infections HSDN C0030193 Sense of pain C0037355 Smallpox vaccines HSDN C0010200 Cough symptom C2033294 Papillary squamous cell carcinoma of larynx UMLS C4085211 Pain distress question C0026718 Mucormycosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024959 Maxillary sinusitis HSDN C2096293 Ent surgical result ear vertigo C0034069 Pulmonary fibrosis HSDN C3541349 Syncope C0019054 Hemolysis (disorder) HSDN C4084768 Usual severity vomiting C0041374 Tumor virus infections HSDN C0043094 Weight gain C0013011 Dominance subordination HSDN C1963091 Diarrhea adverse event C0013298 Duodenitis HSDN C0242670 Chronic vegetative state C4085311 Depression - recess HSDN C3463815 Feel fatigue C3887532 Ulceration HSDN C4084773 Bothered by weight gain C0020295 Hydronephrosis HSDN C0746674 Muscle weakness generalized C1704375 Hypophosphatemic rickets MalaCards C0700078 Deep tendon reflex decrease C0268242 Niemann-pick disease, type a MalaCards|HPO C0031315 Phantom limb pain C0149697 Foot injury wound nos HSDN C1963252 Tremor adverse event C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C4084767 Bothered by vomiting C0042331 Migraine variant MalaCards C1963087 Constipation adverse event C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0018991 Paralysis one side of body C0751891 Hemorrhage, hypertensive intracranial HSDN C0036572 Convulsion C0035305 Retinal detachment HSDN C1963281 Vomiting adverse event C3495559 Juvenile arthritis HSDN C0018772 Deafness C0525045 Mood disorders HSDN C1384666 Decreased hearing C0016719 Friedreich ataxia HPO C0040034 Thrombocytopenia C2931167 Maternofetal infection by parvovirus OrphaNet|MalaCards C0151827 Pain eye C0021568 Bites insect stings HSDN C4084769 Vomiting frequency C1962979 Burn adverse event HSDN C0008031 Pain chest C0011860 Diabetes mellitus, non-insulin-dependent HSDN|UMLS C3274924 Have been coughing C0038454 Cerebrovascular accident HSDN C4084788 Have dizziness C0005967 Bone neoplasms HSDN C0278152 Hemifacial spasms C0085541 Epilepsy, frontal lobe HSDN C0038002 Spleen enlargement C0585274 Periodic syndrome HPO C1963090 Dehydration adverse event C0432217 Wolcott-rallison syndrome OrphaNet|HPO C1549543 Administration method - pain C0031762 Photosensitivity disorders HSDN C0024031 Back pain lower back C0027809 Neurilemmoma HSDN C0151825 Ostalgia C0342643 Autosomal recessive hypophosphatemic vitamin d refractory rickets MalaCards C0018681 Headache, cephalalgia C2368011 Periodic headache syndromes in child or adolescent with intractable migraine UMLS C1384666 Decreased hearing C0078981 Arachnoid cysts HSDN C0587050 Lower extremity mass C1534537 Haematoma of leg UMLS C1000483 Genus anemia C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C0426579 Anorexia symptom C3495422 Finding relating to sexuality and sexual activity HSDN C0700078 Deep tendon reflex decrease C2931395 Bulbospinal neuronopathy, x-linked recessive HPO C0042798 Vision dim C0001916 Albinism HSDN C0020672 Body temperature decreased C0027686 Pathologic neovascularization HSDN C0009806 Constipate C2981403 Stage iiic colorectal cancer UMLS C2024878 Cardiovascular surgery result: dyspnea C0867389 Chronic graft-versus-host disease MalaCards C1962972 Proteinuria adverse event C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C4085317 Diarrhea frequency C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C1963184 Nystagmus adverse event C3554605 Mc3dn2 MalaCards C0004134 Dyssynergia C0268569 Intermittent maple syrup urine disease HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0009081 Congenital clubfoot HSDN C0241165 Skin thickening C0267372 Intestinal lymphatic obstruction MalaCards C2984057 Have nausea C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0344315 Mood depressed C0271865 Autoimmune hypoparathyroidism MalaCards C2203646 Jaundice C1857276 Trichohepatoenteric syndrome MalaCards|HPO C0036572 Convulsion C1866927 Smcr HPO C4084774 Have weight loss C0026636 Mouth diseases HSDN C4085210 Usual severity pain C0677838 Grief loss HSDN C1384666 Decreased hearing C0086650 Mps iii d HPO C0035078 Failure kidney C3888104 Glomerulopathy with fibronectin deposits OrphaNet|HPO|MalaCards C0332563 Papulae C0086873 Pseudopelade OrphaNet|MalaCards C0023380 Lethargy C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards|HPO|UMLS C4084784 Diarrhea C0344479 Spinal cord myelodysplasia HSDN C0000737 Abdomen pain C0460137 Push down or depress HSDN C0454644 Delayed language development C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0867389 Chronic graft-versus-host disease MalaCards C1836296 Lower extremity weakness C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO|UMLS C4084775 Usual severity weight loss C0031212 Personality disorders HSDN C0262384 Chest pain atypical C0085610 Sinus bradycardia UMLS C0011991 Loose stools C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C1069915 Vertigo C0000833 Abscess HSDN C4085548 Usual severity dizziness C0038579 Substance abuse, intravenous HSDN C0030552 Paralysis partial C0011630 Dermatomycoses HSDN C4042891 Sleep wake disorders C1456784 Paranoia HSDN C0028738 Nystagmus C0339527 Leber congenital amaurosis OrphaNet|HPO|MalaCards C0037763 Spasm C0032965 Pregnancy complications, infectious HSDN C0018681 Headache, cephalalgia C0262655 Recurrent urinary tract infection HSDN C0000737 Abdomen pain C2983423 Stage iii hepatocellular carcinoma UMLS C4084769 Vomiting frequency C0014547 Epilepsies, partial HSDN C0009421 Comatose C0342273 Transient neonatal diabetes mellitus MalaCards C3815497 Cough C0153416 Malig neop oth spec part oesop MalaCards C0023012 Delay language C3809853 Mental retardation, autosomal recessive 39 MalaCards C0522224 Palsied C0033581 Prostatitis HSDN C1971624 Appetite absent C0236969 Substance-related disorders HSDN C4085222 Nausea C0004364 Autoimmune diseases HSDN C0007398 Catatonic C0006118 Brain neoplasms HSDN C0030193 Sense of pain C0015652 Fascioliasis HSDN C0278152 Hemifacial spasms C0027651 Tumor HSDN C2024878 Cardiovascular surgery result: dyspnea C0040558 Toxoplasmosis HSDN C0037763 Spasm C0038048 Sprains and strains HSDN C4084802 Usual severity diarrhea C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0262384 Chest pain atypical C0747057 Organic heart disease UMLS C0151786 Weakness muscle C0027643 Neoplasm recurrence, local HSDN C1260922 Respiratory abnormality C3554235 Joubert syndrome 20 MalaCards C2024893 Cardiovascular surgery result: fatigue C0004442 Avoidance learning HSDN C0241165 Skin thickening C0206647 Dermatofibrosarcoma MalaCards C0011991 Loose stools C0022650 Kidney calculi HSDN C4085317 Diarrhea frequency C0870082 Hyperkeratosis HSDN C0036572 Convulsion C0010692 Cystitis HSDN C3539893 Pelvic pain occurs with intercourse C0206687 Carcinoma, endometrioid HSDN C0013404 Respiratory difficulty C0036472 Scrub typhus MalaCards C2919142 Short stature adverse event C3809691 Short-rib thoracic dysplasia 8 with or without polydactyly MalaCards C0008031 Pain chest C0080107 Fistula, respiratory tract HSDN C4084773 Bothered by weight gain C2911243 Encounter due to family history of colonic polyps HSDN C0917816 Deficiency mental C1837454 Spinocerebellar ataxia 8 MalaCards C1963091 Diarrhea adverse event C0678202 Granulomatous enteritis MalaCards C4085862 Bothered by nausea C1457883 Aggressive reaction HSDN C4084802 Usual severity diarrhea C0003872 Arthritis, psoriatic HSDN C0015469 Facial paralysis C0005586 Bipolar disorder HSDN C0038990 Sweats C0751919 Acquired neuromyotonia OrphaNet|MalaCards C0042963 Symptoms vomiting C0017185 Gastrointestinal neoplasms HSDN C0027796 Neuralgias C1720983 Channelopathies HSDN C0013604 Edematous C0006110 Brain death HSDN C0018991 Paralysis one side of body C0700095 Central neuroblastoma HSDN C2911647 Weight gain adverse event C0025500 Mesothelioma HSDN C0036572 Convulsion C0342643 Autosomal recessive hypophosphatemic vitamin d refractory rickets MalaCards C4085210 Usual severity pain C0002892 Anemia, pernicious HSDN C1959630 Eye pain adverse event C0677607 Hashimoto disease HSDN C0013404 Respiratory difficulty C0750426 Wbc elevated HSDN C4084726 Distress cough C0030807 Pemphigus, nos HSDN C4085210 Usual severity pain C1541646 Spirituality therapy HSDN C3539022 Pelvic pain decreasing in severity C0036864 Sexual relations HSDN C0221232 Welts C0263610 Sunlight-induced angio-edema-urticaria UMLS C0700590 Diaphoresis excessive C0001080 Achondroplasia OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0013884 Filarial elephantiases HSDN C0035232 Diaphragmatic paralysis C0007222 Cardiovascular diseases HSDN C0085636 Light sensitivity C0238286 Mucolipidosis type iv OrphaNet|UMLS|HPO|MalaCards C0009421 Comatose C1963198 Pancreatitis adverse event HSDN C4084784 Diarrhea C0043046 Wasting syndrome HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3463824 Myelodysplastic syndrome HSDN C3641756 Have diarrhea C3668816 Inflammation of non-human mammary gland HSDN C4084774 Have weight loss C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards|HSDN C0520909 Ponv C0038536 Subcutaneous emphysema HSDN C0151786 Weakness muscle C0020428 Hyperaldosteronism MalaCards C0149793 Transient monocular blindness C1333990 Hereditary nonpolyposis colorectal cancer MalaCards|HPO C0027424 Congestion nasal C0339852 Dermoids nasal MalaCards C0851578 Disorder sleep C0002989 Epithelioid hemangioma of skin HSDN C1962972 Proteinuria adverse event C0344423 Atrial flutter by ecg finding HSDN C4084774 Have weight loss C0004352 Autistic disorder HSDN C1557397 Adverse event associated with pain C0001173 Adult pyloric stenosis HSDN C4042891 Sleep wake disorders C0029456 Osteoporosis HSDN C1963281 Vomiting adverse event C0024788 Green monkey virus disease DiseaseOntology|MalaCards C2911647 Weight gain adverse event C0001430 Adenoma HSDN C4084723 Constipation C0018378 Guillain-barre syndrome HSDN C0271215 Blindness legal C1336537 Supratentorial meningioma MalaCards C3539890 Pelvic pain causes awakening at night C0019065 Hemorrhage intraperitoneal HSDN C0013608 Cardiac edema C0018805 Heart injuries HSDN C0022568 Inflammation corneal C0406704 Rudiger syndrome 1 OrphaNet|HPO C4085222 Nausea C0019080 Hemorrhage HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013363 Dysautonomia HSDN C0518090 Frequency of pain question C1412084 Abcd1 gene HSDN C1963170 Hypothermia adverse event C0795623 Hepatitis a vaccine, inactivated HSDN C0002170 Alopecia disorders C2931654 Pfeiffer kapferer syndrome MalaCards C3829611 Nausea frequency C0002986 Fabry disease MalaCards|HPO C0035232 Diaphragmatic paralysis C0019285 Diaphragmatic hernia traumatic HSDN C0271215 Blindness legal C0033375 Prolactinoma MalaCards|HPO C4084723 Constipation C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C0011991 Loose stools C0037421 Social isolation HSDN C4084767 Bothered by vomiting C0020303 Hydropneumothorax HSDN C3274924 Have been coughing C0025289 Meningitis HSDN C0018772 Deafness C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards|HPO C4085211 Pain distress question C0085433 Acquired joint deformities HSDN C4084773 Bothered by weight gain C0021831 Intestinal diseases HSDN C3829611 Nausea frequency C0034067 Pulmonary emphysema HSDN C2237041 Shox gene with short stature C1855772 Absent corpus callosum cataract immunodeficiency OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0085920 Brachial neuralgia MalaCards C0015230 Exanthem C1535939 Pneumocystis jiroveci pneumonia UMLS C4018871 Abnormality of the respiratory system C0032326 Pneumothorax MalaCards C0018808 Murmur C0004238 Atrial fibrillation HSDN C1963184 Nystagmus adverse event C1859570 Bardet-biedl syndrome 12 HPO C1963093 Dizziness adverse event C1550672 Specimen type - ulcer HSDN C0013404 Respiratory difficulty C0854970 Adenosquamous cell lung carcinoma recurrent UMLS C0030486 Extremity paralysis, lower C0004275 Attitude health HSDN C3887638 Failure to thrive in infant C0220704 Shprintzen syndrome MalaCards|HPO C0032617 High urine output C0022680 Polycystic kidney diseases HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0039538 Teratoma HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0022650 Kidney calculi HSDN C0028738 Nystagmus C1839730 Prieto x-linked mental retardation syndrome MalaCards C3641756 Have diarrhea C1290398 Cerebral arterial aneurysm HSDN C0040822 D tremors C3150756 Chromosome 4q21 deletion syndrome MalaCards C3274924 Have been coughing C0040034 Thrombocytopenia HSDN C0424755 Fever symptoms C0024620 Primary malignant neoplasm of liver MalaCards C0015300 Ocular proptosis C2678503 Axenfeld-rieger syndrome, type 3 MalaCards|HPO C0018772 Deafness C0005744 Blepharophimosis HSDN C2024878 Cardiovascular surgery result: dyspnea C3161104 Adult plch MalaCards C2024893 Cardiovascular surgery result: fatigue C0023890 Liver cirrhosis HSDN C4085862 Bothered by nausea C0002351 Altitude sickness HSDN C0023380 Lethargy C3888013 Hypnoses HSDN C0030486 Extremity paralysis, lower C0238419 Fournier gangrene HSDN C0013428 Painful urination C0025568 Metaplasia HSDN C0030486 Extremity paralysis, lower C0027059 Myocarditis HSDN C0010200 Cough symptom C0241158 Cicatrix skin HSDN C0036396 Sciatica C0004623 Bacterial infections HSDN C0008031 Pain chest C3463824 Myelodysplastic syndrome HSDN C3898969 Have been vomiting C0043515 Zollinger-ellison syndrome HSDN C0026838 Spasticity muscle C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease OrphaNet|HPO C0020578 Hyperventilate C0001973 Alcoholic intoxication, chronic HSDN C4084727 Cough frequency C0036974 Shock HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038220 Status epilepticus HSDN C0025287 Meningitis-like C0155490 Middle ear cholesteatoma HSDN C1279888 Proteinuria of undiagnosed cause C0040128 Thyroid diseases HSDN C4084784 Diarrhea C3888013 Hypnoses HSDN C2203646 Jaundice C0020502 Hyperparathyroidism HSDN C2984057 Have nausea C0025007 Measles HSDN C1961131 Cough adverse event C0040553 Toxocariasis HSDN C3541349 Syncope C0007820 Cerebrovascular disorders HSDN C4084723 Constipation C0007095 Carcinoid tumor HSDN C0015469 Facial paralysis C0796002 Johnson-mcmillin syndrome MalaCards C0860603 Anxiety symptom C3810225 Mental retardation, autosomal recessive 41 MalaCards C3274924 Have been coughing C0340848 Pulmonary venoocclusive disease 2, autosomal recessive HPO C3815497 Cough C0023241 Legionnaires' disease OrphaNet|MalaCards C2237041 Shox gene with short stature C0795942 Fitzsimmons-guilbert syndrome HPO C0019572 Hairiness C0025874 Metrorrhagia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0600564 Self-efficacy HSDN C2037133 Sudden loss of vision in right half of visual field C0018979 Hemianopsia UMLS C0035229 Respiratory function impaired C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C1145628 Autonomic nervous system disorders HSDN C0030552 Paralysis partial C0376175 Bell palsy HSDN C2919142 Short stature adverse event C1839125 Say-meyer syndrome MalaCards C0015469 Facial paralysis C0026266 Mitral valve insufficiency HSDN C3463815 Feel fatigue C0021051 Immunologic deficiency syndromes HSDN C0424755 Fever symptoms C0031212 Personality disorders HSDN C0085636 Light sensitivity C3554610 Cone-rod dystrophy 17 MalaCards|UMLS C0233514 Behavior abnormal C4014531 Epileptic encephalopathy, early infantile, 24 MalaCards C1384666 Decreased hearing C0004623 Bacterial infections HSDN C1549543 Administration method - pain C0002989 Epithelioid hemangioma of skin HSDN C0022346 Yellow skin C0034069 Pulmonary fibrosis HSDN C0002622 Amnesias C0007772 Intracranial arteriovenous malformation HSDN C3665346 Loss sight C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards|HPO C0027796 Neuralgias C0032344 Poisoning aspects HSDN C0036396 Sciatica C0008925 Cleft palate HSDN C0003962 Ascites C2931872 Free sialic acid storage disease OrphaNet|MalaCards C0518090 Frequency of pain question C0085433 Acquired joint deformities HSDN C1963093 Dizziness adverse event C0036974 Shock HSDN C4042891 Sleep wake disorders C0233629 Thinking and speaking disturbances HSDN C3274924 Have been coughing C0019621 Histiocytosis, langerhans-cell HSDN C1279888 Proteinuria of undiagnosed cause C0206247 Amyloid neuropathies HSDN C0270274 Newborn vomiting C0267173 Vomiting in infants and children UMLS C0020673 Hypothermia (central) (local) C0003850 Arteriosclerosis HSDN C2029884 Hearing loss by exam C0034530 Injury radiation HSDN C2024893 Cardiovascular surgery result: fatigue C0021831 Intestinal diseases HSDN C0036572 Convulsion C1852296 Darier disease, acral hemorrhagic type HPO C0015469 Facial paralysis C0013261 Duane retraction syndrome HSDN C0232462 Appetite decrease C0854176 Malignant hepato-biliary neoplasm MalaCards C0008031 Pain chest C0007785 Cerebral infarction HSDN C0270948 Neurogenic muscular atrophy C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C0015469 Facial paralysis C0751878 Vasculitis, central nervous system HSDN C1963252 Tremor adverse event C0860603 Anxiety symptoms HSDN C0020455 Hypergammaglobulinemia C0029185 Orbit tumor HSDN C0037199 Sinus infection C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C0043094 Weight gain C0026857 Musculoskeletal diseases HSDN C0042024 Urine incontinence C0011168 Deglutition disorders HSDN C4084724 Usual severity constipation C0007789 Cerebral palsy HSDN C0030232 Color loss C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C0024031 Back pain lower back C0019326 Ventral hernia HSDN C1557397 Adverse event associated with pain C0079218 Fibromatosis, aggressive HSDN C0015732 Feces incontinence C0011644 Scleroderma OrphaNet|MalaCards C4085661 Usual severity nausea C1847839 Episodic ataxia, type 3 MalaCards C0009792 Consciousness disorder C0751815 Carotid artery, internal, dissection HSDN C0022346 Yellow skin C0022660 Kidney failure, acute UMLS C0013405 Dyspnea, paroxysmal C0149514 Bronchitis acute HSDN C2032396 Pelvic pain on the right C0002989 Epithelioid hemangioma of skin HSDN C0028738 Nystagmus C1853116 Spinocerebellar ataxia, autosomal recessive 8 (disorder) MalaCards|HPO C0018784 Deafness sensorineural C0022758 Kap HSDN C1963249 Tinnitus adverse event C0206721 Inverted papilloma HSDN C0518090 Frequency of pain question C2219717 Menstrual periods stopped for over 6 months HSDN C1384666 Decreased hearing C1837501 Microcephaly, primary autosomal recessive, 5 MalaCards|HPO C1384666 Decreased hearing C1859329 Cardioauditory syndrome of sanchez cascos MalaCards C3539889 Pelvic pain increasing in severity C0029456 Osteoporosis HSDN C0151825 Ostalgia C0015306 Hereditary multiple exostoses OrphaNet|HPO C1963281 Vomiting adverse event C0010692 Cystitis HSDN C3463815 Feel fatigue C0003851 Arteriosclerosis obliterans HSDN C0242936 Center pain C0036421 Systemic scleroderma HSDN C2984058 Have pain C0018805 Heart injuries HSDN C4085661 Usual severity nausea C0022336 Creutzfeldt-jakob disease HSDN C0039870 Leanness C0020459 Hyperinsulinism HSDN C3641755 Have constipation C0042487 Venous thrombosis HSDN C0036572 Convulsion C0032310 Pneumonia, viral HSDN C1510417 Apraxia of gait C0027877 Neuronal ceroid-lipofuscinoses HSDN C4085211 Pain distress question C0014805 Primary erythermalgia HPO C4085317 Diarrhea frequency C0016169 Pathologic fistula HSDN C2237041 Shox gene with short stature C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C1549543 Administration method - pain C0004782 Basal ganglia diseases HSDN C0035078 Failure kidney C3854315 Pseudoprimary hyperaldosteronism MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0025637 Methemoglobinemia HSDN C0018772 Deafness C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0236969 Substance-related disorders HSDN C0008031 Pain chest C0018188 Granuloma HSDN C1963274 Vasculitis adverse event C0019250 Hereditary factor i deficiency disease MalaCards C0234533 Seizure generalized C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C2315100 Pediatric failure to thrive C0006849 Oral candidiasis HSDN C0030200 Intractable pain C0007137 Squamous cell carcinoma HSDN C0232493 Epigastric pain C1833541 Caroli disease isolated MalaCards C0036572 Convulsion C0031069 Familial mediterranean fever OrphaNet|HSDN|HPO C4085317 Diarrhea frequency C0026636 Mouth diseases HSDN C3274924 Have been coughing C1800706 Idiopathic pulmonary fibrosis MalaCards|HSDN C0270274 Newborn vomiting C0852271 Neonatal digestive disorders UMLS C1549543 Administration method - pain C0033324 Prognathism HSDN C0036396 Sciatica C0027095 Myosarcoma HSDN C0013421 Dystonia C2751843 Leukoencephalopathy, cystic, without megalencephaly MalaCards|HPO C0043094 Weight gain C0085096 Peripheral vascular diseases HSDN C0747556 Pharyngitis recurrent C0581381 Recurrent upper respiratory tract infection UMLS C4084723 Constipation C0175702 Williams syndrome OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0014511 Epithelial cyst HSDN C0015468 Face pain C0271355 Abducens nerve paralysis HSDN C0518090 Frequency of pain question C0011609 Drug eruptions HSDN C1384666 Decreased hearing C0175699 Saethre-chotzen syndrome MalaCards|HPO C4085549 Dizziness C0003490 Aortic arch syndrome HSDN C0085636 Light sensitivity C1337030 Xpa gene HPO C0018784 Deafness sensorineural C0014038 Encephalitis HSDN C3815497 Cough C0011603 Dermatitis HSDN C4085210 Usual severity pain C0029883 Otitis media with effusion HSDN C0542476 Forgetful C1843014 Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques HPO C0018772 Deafness C0424688 Small head HSDN C0595939 Stillborn C2673477 Hypophosphatasia, perinatal lethal HPO C0016382 Cutaneous vascular engorgement C3873472 Vulvovaginal gingival syndrome MalaCards C4085317 Diarrhea frequency C0038220 Status epilepticus HSDN C0032227 Effusion pleural C0026764 Multiple myeloma HPO C0002962 Angina C0003838 Arterial occlusive diseases HSDN C0577567 Mass of urogenital structure C0403472 Acquired cyst of kidney with neoplastic change UMLS C3829611 Nausea frequency C0038354 Stomach diseases HSDN C0242936 Center pain C0029396 Heterotopic ossification HSDN C0024032 Birth weight subnormal C1846331 Juvenile-onset dystonia MalaCards|HPO C0033377 Caudal displacement C0265261 Multiple pterygium syndrome HPO C0037763 Spasm C0019163 Hepatitis b HSDN C0009806 Constipate C0585274 Periodic syndrome OrphaNet|HPO C0030552 Paralysis partial C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C1963087 Constipation adverse event C0001144 Acne vulgaris HSDN C0028738 Nystagmus C1845116 Nystagmus 5, infantile periodic alternating MalaCards C0009421 Comatose C0014836 Escherichia coli infections HSDN C2911647 Weight gain adverse event C0014038 Encephalitis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1261473 Sarcoma HSDN C0015970 Fever unknown origin C0242994 Hantavirus infections HSDN C0003460 Anurias C1856143 Hemolytic uremic syndrome, typical MalaCards C0018681 Headache, cephalalgia C0027983 Newcastle disease DiseaseOntology|MalaCards C2034124 Paralysis of right leg only C0030486 Paraplegia UMLS C3887873 Hearing loss C2984291 Glioblastoma multiforme pathway HSDN C4085211 Pain distress question C0008088 Child psychiatry HSDN C0018681 Headache, cephalalgia C0276289 Zika virus infection MalaCards C0037771 Paraparesis spastic C0338437 Neurocysticercosis HSDN C1963087 Constipation adverse event C1962963 Osteoporosis adverse event HSDN C3829611 Nausea frequency C0812393 Cancer patients and suicide and depression HSDN C0151786 Weakness muscle C0011881 Diabetic nephropathy HSDN C1279888 Proteinuria of undiagnosed cause C0268250 Gaucher disease, type 2 (disorder) MalaCards C0016199 Pain flank C0879257 Hereditary papillary renal carcinoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0030783 Pellagra HSDN C0857305 Thrombocytopenia purpura C0347555 Friction blister HSDN C1963086 Confusion adverse event C0022116 Ischemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030100 Oxyuriasis HSDN C0237326 Defecation pain C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards C4085548 Usual severity dizziness C0038395 Streptococcal infections HSDN C4084727 Cough frequency C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0857305 Thrombocytopenia purpura C0036421 Systemic scleroderma HSDN C0007758 Cerebellar ataxia C1859301 Cerebellar hypoplasia with endosteal sclerosis MalaCards C0042928 Paralysis vocal cord C0270611 Brain damage HSDN C0576456 Poor feeding C3280479 Pitt-hopkins-like syndrome 2 MalaCards C4085211 Pain distress question C0014742 Erythema multiforme HSDN C4084768 Usual severity vomiting C0460137 Push down or depress HSDN C2984058 Have pain C0014461 Granuloma eosinophilic HSDN C0522224 Palsied C0011884 Diabetic retinopathy HSDN C0013404 Respiratory difficulty C0004045 Asphyxia neonatorum HSDN C3641755 Have constipation C0004935 Animal ethology HSDN C0035229 Respiratory function impaired C0238027 Botulism, infantile MalaCards C3887638 Failure to thrive in infant C3151113 Meier-gorlin syndrome 3 MalaCards|HPO C4084767 Bothered by vomiting C0034531 Experimental radiation injuries HSDN C4084776 Weight loss C0002792 Anaphylaxis HSDN C2984058 Have pain C0017075 Ganglioneuroma HSDN C0003862 Pain joint C0031090 Periodontal diseases HSDN C2911645 Weight loss adverse event C0004943 Behcet syndrome MalaCards|HSDN|HPO C0018775 Hearing loss bilateral C0002395 Alzheimer's disease HSDN C0234146 Absent reflex C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C3541349 Syncope C2937358 Cerebral hemorrhage HSDN C0700078 Deep tendon reflex decrease C0003708 Arachnitis OrphaNet|MalaCards C1557397 Adverse event associated with pain C0014335 Enteritis HSDN C0004604 Pain back C0023290 Leishmaniasis, visceral HSDN C4084776 Weight loss C0007099 Carcinoma in situ HSDN C0036572 Convulsion C2931241 Primary intestinal lymphangiectasis MalaCards C0349588 Stature short C0796088 Neurofaciodigitorenal syndrome OrphaNet|MalaCards C0005745 Blepharoptosis C1843225 Charcot-marie-tooth disease, axonal, type 2e (disorder) HPO C1963184 Nystagmus adverse event C1855995 L-2-hydroxyglutaric aciduria MalaCards|HPO C0018681 Headache, cephalalgia C3714602 Staphylococcal toxic shock syndrome MalaCards C0002962 Angina C0020615 Hypoglycemia HSDN C4084727 Cough frequency C0020538 Hypertensive disease HSDN C4085211 Pain distress question C1963211 Pericarditis adverse event HSDN C3887638 Failure to thrive in infant C0008925 Cleft palate HSDN C1999266 Depression adverse event C3810230 Neurodegeneration with brain iron accumulation 6 MalaCards C0002962 Angina C0024419 Waldenstrom macroglobulinemia HSDN C0036572 Convulsion C0002438 Amebiasis HSDN C1253937 Pericardial effusion C0267372 Intestinal lymphatic obstruction MalaCards C0009792 Consciousness disorder C0031391 Phencyclidine abuse HSDN C4085317 Diarrhea frequency C0004576 Babesiosis HSDN C1963281 Vomiting adverse event C1563706 Nephrogenic diabetes insipidus, type ii HPO C0030193 Sense of pain C0853986 Lymphocytes decreased HSDN C4042891 Sleep wake disorders C1510586 Autism spectrum disorders HSDN C0521483 Mucous hyperplasia C1290782 Verrucous hyperplasia of oral mucosa UMLS C2984057 Have nausea C0032269 Pneumococcal infections HSDN C0243026 Generalized infection C0221026 X-linked agammaglobulinemia OrphaNet|HPO C0013404 Respiratory difficulty C1710174 Squamous cell lung carcinoma, clear cell variant UMLS C0013404 Respiratory difficulty C0016085 Filariasis HSDN C0042024 Urine incontinence C1849128 Spastic paraplegia 15, autosomal recessive MalaCards|HPO C0025287 Meningitis-like C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C2911645 Weight loss adverse event C0206255 Malaria vaccine HSDN C0231341 Aging premature C0376634 Craniofacial abnormalities HSDN C4084768 Usual severity vomiting C0796003 Juberg-marsidi syndrome HPO C1963087 Constipation adverse event C0271585 Isolated trh deficiency MalaCards C0015469 Facial paralysis C0020473 Hyperlipidemia HSDN C0016199 Pain flank C0206674 Adenoma, villous HSDN C0030193 Sense of pain C0020564 Hypertrophy HSDN C0010200 Cough symptom C1550639 Specimen type - fistula HSDN C0349588 Stature short C0342280 Aredyld OrphaNet|MalaCards C0013604 Edematous C0007282 Carotid stenosis HSDN C0857305 Thrombocytopenia purpura C0004096 Asthma HSDN C4084802 Usual severity diarrhea C0042974 Von willebrand disease HSDN C0002963 Angina variant C0919267 Ovarian neoplasm HSDN C0013404 Respiratory difficulty C0024214 Lymphangiectasis HSDN C2919142 Short stature adverse event C1851996 Dwarfism tall vertebrae OrphaNet|HPO C0042798 Vision dim C0041296 Tuberculosis HSDN C0022568 Inflammation corneal C0079583 Ichthyosiform erythroderma, congenital MalaCards C0022346 Yellow skin C0270958 Kocher-debre-semelaigne syndrome OrphaNet|MalaCards C0424755 Fever symptoms C0016627 Avian influenza DiseaseOntology|HSDN|MalaCards C0015468 Face pain C0399526 Class iii malocclusion HSDN C1963281 Vomiting adverse event C1456865 Ureteral calculi HSDN C0040822 D tremors C0024473 Magnesium deficiency HSDN C0042571 Vertigo subjective C0003507 Aortic valve stenosis HSDN C0013604 Edematous C0014118 Endocarditis HSDN C1963137 Hydrocephalus adverse event C4014742 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 MalaCards C2984057 Have nausea C0043352 Xerostomia HSDN C3641755 Have constipation C0342257 Complications of diabetes mellitus HSDN C0344428 Ventricular tachycardia by ecg finding C3151264 Cardiomyopathy, familial hypertrophic, 17 HPO C2203646 Jaundice C2675184 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C1704272 Benign prostatic hyperplasia HSDN C0020672 Body temperature decreased C0007762 Cerebellar neoplasms HSDN C0030554 Abnormal sensation C0038016 Spondylolisthesis HSDN C0030193 Sense of pain C0026771 Trauma multiple HSDN C0004604 Pain back C1290398 Cerebral arterial aneurysm HSDN C3146279 Coma C0026850 Muscular dystrophy HSDN C0037383 Sneeze C0035243 Respiratory tract infections HSDN C0039070 Collapse fleeting C2678476 Cardiomyopathy, dilated, 1y MalaCards C4084774 Have weight loss C0033968 Psychotherapeutic technique HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027765 Nervous system disorder HSDN C0009792 Consciousness disorder C0007274 Carotid artery thrombosis HSDN C4084775 Usual severity weight loss C0243026 Sepsis HSDN C0004134 Dyssynergia C0266470 Cerebellar hypoplasia OrphaNet C0587051 Lumbar mass C4075816 Neoplasm of lumbar spinal nerve UMLS C0019079 Bloody sputum C0017181 Gastrointestinal hemorrhage HSDN C0000737 Abdomen pain C0854789 Resectable carcinoma of small bowel UMLS C0233794 Memory impaired C1833296 Frontotemporal dementia, chromosome 3-linked HPO C0038002 Spleen enlargement C1849435 Bicarbonate-wasting rta OrphaNet|HPO C0003962 Ascites C3273031 Hnec MalaCards C1963091 Diarrhea adverse event C0037997 Splenic diseases HSDN C0011168 Disorder deglutition C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C2911645 Weight loss adverse event C0014356 Enterocolitis HSDN C0221166 Paraparesis C0085261 Proteus syndrome HSDN C4085642 Level of joint stiffness C0220722 Cerebrooculofacioskeletal syndrome 1 OrphaNet|HPO C0042940 Disorder of voice C0031347 Pharyngeal neoplasms HSDN C0027796 Neuralgias C0042138 Uterine neoplasms HSDN C4084723 Constipation C0020473 Hyperlipidemia HSDN C4085661 Usual severity nausea C3150933 Hyperaldosteronism, familial, type iii MalaCards C0016382 Cutaneous vascular engorgement C0043515 Zollinger-ellison syndrome MalaCards C0020505 Excessive eating C0021670 Insulinoma OrphaNet|HPO|MalaCards C0240419 Tenderness muscle C0036231 Sarcocystosis DiseaseOntology C4084723 Constipation C0242698 Ventricular dysfunction, left HSDN C0020538 Hbp C2931253 Alport syndrome, dominant type MalaCards C0020450 Hyperemesis gravidarum C0011175 Dehydration HSDN C0040822 D tremors C0268151 Classical galactosemia MalaCards|HPO C0019209 Large liver C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C2024878 Cardiovascular surgery result: dyspnea C1857688 Telangiectasia, hereditary hemorrhagic, type 4 MalaCards C0424755 Fever symptoms C0276286 Onyong-nyong fever MalaCards C2242996 Tingling C0031036 Polyarteritis nodosa HSDN C3887873 Hearing loss C0005686 Urinary bladder diseases HSDN C0917816 Deficiency mental C0795887 Chromosome xp21 deletion syndrome MalaCards C0002962 Angina C0018235 Aggrieved HSDN C0917816 Deficiency mental C2751318 Nijmegen breakage syndrome-like disorder MalaCards|HPO C4084784 Diarrhea C0268407 Senile cardiac amyloidosis MalaCards C0008031 Pain chest C0024788 Green monkey virus disease DiseaseOntology|OrphaNet|MalaCards C4084775 Usual severity weight loss C0036117 Salmonella infections HSDN C0042024 Urine incontinence C0342727 3-@methylglutaconic aciduria, type i MalaCards|HPO C4020887 Photodysphoria C0343057 Keratosis pilaris decalvans HPO C0042798 Vision dim C4015424 Retinal dystrophy and obesity MalaCards C4085210 Usual severity pain C0033806 Pseudohypoparathyroidism HSDN C4085862 Bothered by nausea C0024788 Green monkey virus disease DiseaseOntology|MalaCards C0000727 Abdomen acute C0700095 Central neuroblastoma HSDN C0013428 Painful urination C0037930 Spinal cord neoplasms HSDN C0349588 Stature short C3151187 Seckel syndrome 5 MalaCards C0004134 Dyssynergia C3553538 Brown-vialetto-van laere syndrome 2 MalaCards|UMLS C0018772 Deafness C0453996 Tobacco smoking HSDN C0005745 Blepharoptosis C1867440 Multiple pterygium syndrome, autosomal dominant MalaCards|HPO C0231712 Gait waddling C3501858 Muscular dystrophy, limb-girdle, type 1d MalaCards C0009676 Confusion state C0007873 Uterine cervical neoplasm HSDN C1963087 Constipation adverse event C0023176 Lead poisoning MalaCards|HSDN C0242936 Center pain C0005396 Bile duct neoplasms HSDN C0015672 Decreased energy C0001627 Congenital adrenal hyperplasia HSDN C0000737 Abdomen pain C2981379 Stage iib small intestinal cancer UMLS C0015469 Facial paralysis C0700095 Central neuroblastoma HSDN C0028738 Nystagmus C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C0086565 Liver function abnormal C1304456 Congo hemorrhagic fever MalaCards C0036572 Convulsion C0007798 Cerebral ventricle neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001327 Laryngitis acute HSDN C4050613 Anxiety C2675369 Chromosome 22q11.2 microduplication syndrome HPO C4084769 Vomiting frequency C0021051 Immunologic deficiency syndromes HSDN C0036572 Convulsion C0393723 Writing epilepsy UMLS C0018926 Emesis bloody C1000483 Genus anemia HSDN C0015402 Hemorrhage eye C0221269 Pseudolymphoma HSDN C1557397 Adverse event associated with pain C0340629 Aortic aneurysm without mention of rupture nos HSDN C0085636 Light sensitivity C1857569 Corneal endothelial dystrophy 2 MalaCards C0039870 Leanness C0037744 Perceptual spatial orientation HSDN C0878773 Bladder hyperactive C2717837 Drug-induced liver injury, chronic HSDN C0018777 Deafness, conductive C1860789 Leukemia, megakaryoblastic, of down syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0027086 Myoma HSDN C0853698 Lymphocytes increased C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0028738 Nystagmus C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C0948698 Coronary spastic angina C0002963 Angina pectoris, variant UMLS C4084775 Usual severity weight loss C0026848 Myopathy HSDN C0040034 Thrombocytopenia C1846421 Lathosterolosis OrphaNet|HPO|MalaCards C0002624 Amnesia retrograde C0394016 Coma, post-head injury HSDN C3539890 Pelvic pain causes awakening at night C0021831 Intestinal diseases HSDN C4084766 Vomiting C0020445 Hypercholesterolemia, familial HSDN C0270948 Neurogenic muscular atrophy C2931587 Gemignani syndrome OrphaNet|MalaCards C0030552 Paralysis partial C0020225 Hydranencephaly HSDN C0022346 Yellow skin C0037356 Smallpox virus HSDN C4085210 Usual severity pain C0017662 Glomerulonephritis, membranoproliferative HSDN C0039070 Collapse fleeting C0000768 Congenital abnormality HSDN C3539892 Pelvic pain in front C0206680 Mesothelioma, cystic HSDN C0238532 Abdomen scaphoid C0264200 Acquired deformity of the abdomen, nos UMLS C0151827 Pain eye C0015423 Eyelid diseases HSDN C2911647 Weight gain adverse event C0006109 Brain damage, chronic HSDN C3898969 Have been vomiting C0020625 Hyponatremia HSDN C3641756 Have diarrhea C0027662 Multiple endocrine neoplasia HSDN C0009763 Conjunctiva inflammation C3150354 Immunodeficiency, common variable, 2 MalaCards|HPO C0015468 Face pain C0333355 Inflammatory disease of mucous membrane HSDN C0011168 Disorder deglutition C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C0575081 Abnormal gait C0265280 Spondylometaphyseal dysplasia, kozlowski type OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0919267 Ovarian neoplasm HSDN C3163620 Hypotension adverse event C0023788 Whipple disease OrphaNet|MalaCards C4084726 Distress cough C0004153 Atherosclerosis HSDN C0751837 Gait ataxic C0019841 Classical swine fever HSDN C3887638 Failure to thrive in infant C0037315 Sleep apnea syndromes HSDN C4084776 Weight loss C0860549 Refeed syndrome HSDN C0520909 Ponv C0023976 Long qt syndrome HSDN C0011206 Delirium acute C0018801 Heart failure HSDN C0003811 Cardiac rhythm disturbance C0406723 Growth retardation, alopecia, pseudoanodontia and optic atrophy MalaCards C0004134 Dyssynergia C0005695 Bladder neoplasm HSDN C0018932 Bright red rectal bleeding C1868081 Juvenile polyposis coli HPO C0011991 Loose stools C0037322 Active eye movement sleep HSDN C0424755 Fever symptoms C0004275 Attitude health HSDN C4085211 Pain distress question C0030424 Paragonimiasis HSDN C2024878 Cardiovascular surgery result: dyspnea C0024110 Pulmonary abscess HSDN C0018681 Headache, cephalalgia C0009373 Colonic diseases HSDN C4085317 Diarrhea frequency C1258104 Diffuse scleroderma HSDN C0027497 Queasy C1336856 Anaplastic carcinoma of extrahepatic bile duct UMLS C1557397 Adverse event associated with pain C0001349 Acute-phase reaction HSDN C3463815 Feel fatigue C0919267 Ovarian neoplasm HSDN C0015672 Decreased energy C3541306 Plasmodium measurement HSDN C2984057 Have nausea C0162565 Acute intermittent porphyria MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0026946 Mycoses HSDN C0009806 Constipate C0206171 Community acquired infections HSDN C0007815 Cerebrospinal fluid rhinorrhoea C3203727 Pneumorrhachi HSDN C0023380 Lethargy C0271972 Thiamine-responsive megaloblastic anemia MalaCards C2362324 Pediatric obesity C4042784 Feeding and eating disorders HSDN C1260880 Nasal drip C3899651 Childhood nasal cavity carcinoma UMLS C4084774 Have weight loss C0011615 Dermatitis, atopic HSDN C0024031 Back pain lower back C0037369 Smoking HSDN C3665386 Abnormal vision C0010481 Cushing syndrome HPO C0035078 Failure kidney C0002726 Amyloidosis OrphaNet|MalaCards C0002622 Amnesias C0038220 Status epilepticus HSDN C2984057 Have nausea C1704212 Embolism embolus HSDN C0020455 Hypergammaglobulinemia C1279945 Acute interstitial pneumonia MalaCards C0042963 Symptoms vomiting C2028283 History of premature birth HSDN C4084775 Usual severity weight loss C1861172 Venous thromboembolism HSDN C3539895 Pelvic pain occurs with bowel movement C0262655 Recurrent urinary tract infection HSDN C0030552 Paralysis partial C0013473 Eating disorders HSDN C0020672 Body temperature decreased C0018818 Ventricular septal defects HSDN C0027066 Myoclonic jerking C0002395 Alzheimer's disease HSDN C2364111 Gustatory anesthesia C0006849 Oral candidiasis HSDN C0030975 Disorders perception C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0002962 Angina C0549567 Pigmentation disorders HSDN C0150055 Pain chronic C1723764 Chronic prostatitis with chronic pelvic pain syndrome UMLS C2024893 Cardiovascular surgery result: fatigue C0221026 X-linked agammaglobulinemia OrphaNet|HPO C0015799 Feminisation C0016697 Freemartinism HSDN C0454644 Delayed language development C0268553 Hyperlysinemias HPO C0023012 Delay language C1412747 Bbs2 gene HPO C4085222 Nausea C0717360 Disease lyme vaccine HSDN C1145670 Failure respiratory C1861922 Campomelic dysplasia OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0035229 Respiratory function impaired C0796028 Ataxia, fatal x-linked, with deafness and loss of vision OrphaNet|HPO|MalaCards C0027498 Nausea vomiting C0391826 Lhermitte-duclos disease OrphaNet|HPO|MalaCards C0035229 Respiratory function impaired C0024776 Maple syrup urine disease OrphaNet C0151786 Weakness muscle C1704375 Hypophosphatemic rickets OrphaNet|HPO|MalaCards C0004941 Behavioral symptoms C0162531 Hereditary coproporphyria OrphaNet C0041657 Consciousness loss C0030482 Paraepithymia HSDN C0018681 Headache, cephalalgia C1834559 Continuous muscle fiber activity, hereditary HPO C0518090 Frequency of pain question C0028796 Dermatitis, occupational HSDN C0020672 Body temperature decreased C0009240 Cognition HSDN C0015672 Decreased energy C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0018834 Brash C1328479 Pancreatic endocrine carcinoma HSDN C2096293 Ent surgical result ear vertigo C0011551 Depersonalisation HSDN C3829611 Nausea frequency C0024841 Matrimony, matrimonial HSDN C1963087 Constipation adverse event C0009376 Colonic polyps HSDN C0023530 Leukopenia C3810350 Bone marrow failure syndrome 2 MalaCards C0018989 Paresis of one side of body C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C0030975 Disorders perception C0338451 Frontotemporal dementia HSDN C2919142 Short stature adverse event C2931420 Brachydactylous dwarfism mseleni type OrphaNet|MalaCards C0008031 Pain chest C0032226 Pleural diseases HSDN C0575081 Abnormal gait C3537167 Trisomy 21 MalaCards C4084802 Usual severity diarrhea C0002986 Fabry disease MalaCards|HPO C0009792 Consciousness disorder C0428977 Bradycardia HSDN C1557397 Adverse event associated with pain C0005417 Bile duct fistula HSDN C0039070 Collapse fleeting C0003469 Anxiety disorders HSDN C0034933 Abnormal reflexes C0003462 Anus diseases HSDN C0012569 Double vision C2984289 Melanoma pathway HSDN C0037384 Snore C1305740 Overbite HSDN C4085210 Usual severity pain C2188545 Anuria HSDN C0917816 Deficiency mental C3540662 Congenital amaurosis of retinal origin MalaCards C0015970 Fever unknown origin C0236969 Substance-related disorders HSDN C1557397 Adverse event associated with pain C0005818 Blood platelet disorders HSDN C0042571 Vertigo subjective C0036323 Schistosomiasis HSDN C2911647 Weight gain adverse event C0036982 Shock, hemorrhagic HSDN C0518090 Frequency of pain question C0030319 Panic disorder HSDN C0454644 Delayed language development C2930926 Autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes MalaCards C0007758 Cerebellar ataxia C0018553 Hamartoma syndrome, multiple OrphaNet|HPO|MalaCards C0151825 Ostalgia C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy OrphaNet|HPO C0018681 Headache, cephalalgia C0001857 Aids related complex UMLS C0009806 Constipate C1546533 Specimen source codes - abscess HSDN C0020538 Hbp C0752166 Bardet-biedl syndrome OrphaNet|HPO|MalaCards C4084897 Sleep disturbance subordinate domain C1510479 Neuralgic amyotrophy MalaCards|HPO C1963252 Tremor adverse event C0700595 Spinal muscular atrophies of childhood HSDN C0085636 Light sensitivity C1865695 Spondylometaphyseal dysplasia, axial MalaCards C4085222 Nausea C0011265 Presenile dementia HSDN C4084769 Vomiting frequency C0003618 Appetites HSDN C3146279 Coma C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C0521532 Diaphragmatic weakness C0015708 Fazio londe syndrome MalaCards|HPO C1565249 Limitation, mobility C0026847 Spinal muscular atrophy HSDN C2096293 Ent surgical result ear vertigo C2984291 Glioblastoma multiforme pathway HSDN C0043094 Weight gain C0022353 Neonatal jaundice HSDN C0027796 Neuralgias C0019069 Hemophilia a HSDN C0037763 Spasm C0453996 Tobacco smoking HSDN C0036572 Convulsion C0003490 Aortic arch syndrome MalaCards|HSDN C0018784 Deafness sensorineural C0007781 Intracranial embolism and thrombosis HSDN C1549543 Administration method - pain C0014356 Enterocolitis HSDN C1963071 Back pain adverse event C2931038 Pancreatic carcinoma, familial MalaCards C0003862 Pain joint C1848029 Ehlers-danlos syndrome caused by tenascin-x deficiency OrphaNet|HPO|UMLS C0010520 Skin cyanosis C3531896 Fatal congenital nonlysosomal heart glycogenosis MalaCards C4085661 Usual severity nausea C0026961 Mydriasis HSDN C1319540 On examination - left eye preproliferative diabetic retinopathy C0011164 Abnormal degeneration UMLS C4085210 Usual severity pain C0038018 Spondylolysis HSDN C0036396 Sciatica C0018099 Gout HSDN C0018772 Deafness C0012236 Digeorge syndrome OrphaNet|HSDN C3163620 Hypotension adverse event C0001403 Addison disease OrphaNet C0413252 Hypothermia due to exposure C0006285 Bronchopneumonia HSDN C0009676 Confusion state C0002886 Anemia, macrocytic HSDN C0015672 Decreased energy C0855096 Recurrent small lymphocytic lymphoma UMLS C0035229 Respiratory function impaired C1835845 Mitochondrial phosphate carrier deficiency MalaCards|HPO C3274924 Have been coughing C0085092 Parenting behavior HSDN C0151786 Weakness muscle C0041466 Typhoid fever HSDN C0349588 Stature short C0018553 Hamartoma syndrome, multiple MalaCards|HPO C1961131 Cough adverse event C0035235 Respiratory syncytial virus infections MalaCards|HSDN C3887638 Failure to thrive in infant C3810062 Congenital disorder of glycosylation, type iw MalaCards C0042514 Ventricular tachycardia C3808145 Left ventricular noncompaction 9 MalaCards C0242936 Center pain C0019114 Hemosiderosis HSDN C0749851 Upper extremity tingling C0741096 Upper_ext problem UMLS C2911647 Weight gain adverse event C1366535 Avp gene HSDN C1963091 Diarrhea adverse event C0238154 Epidural hematoma HSDN C0454644 Delayed language development C2936346 22q11 deletion syndrome MalaCards C0009792 Consciousness disorder C0729544 Fungal cns infection HSDN C2024893 Cardiovascular surgery result: fatigue C0026530 Morales HSDN C0242936 Center pain C0027721 Lipoid nephrosis HSDN C0002170 Alopecia disorders C0079683 Herlitz disease MalaCards|HPO C4085211 Pain distress question C0080032 Pleural effusion, malignant HSDN C0018784 Deafness sensorineural C0003869 Arthritis, infectious HSDN C1963077 Bone pain adverse event C0410530 Metachondromatosis MalaCards C3898969 Have been vomiting C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C2024893 Cardiovascular surgery result: fatigue C0005396 Bile duct neoplasms HSDN C0019209 Large liver C0268060 Juvenile hemochromatosis MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0016542 Foreign body HSDN C0036572 Convulsion C3809877 Schaaf-yang syndrome MalaCards C3641755 Have constipation C0007193 Cardiomyopathy, dilated HSDN C4084784 Diarrhea C1836706 Hyperthyroidism, nonautoimmune MalaCards C0748546 Scrotum area tender C0741437 Male_repro problem UMLS C0242936 Center pain C0003463 Anus neoplasms HSDN C1384666 Decreased hearing C2931702 Chromosome 14q, terminal duplication OrphaNet|MalaCards C0036572 Convulsion C1845142 Mental retardation, x-linked 91 (disorder) HPO C4084767 Bothered by vomiting C0027873 Neuromyelitis optica HSDN C3829611 Nausea frequency C0029823 Other specif.peritonitis nos DiseaseOntology C0042798 Vision dim C1857277 Donnai-barrow syndrome MalaCards C4084724 Usual severity constipation C0024117 Chronic obstructive airway disease HSDN C4084724 Usual severity constipation C0022650 Kidney calculi HSDN C0033774 Skin pruritus C0024137 Lupus erythematosus, cutaneous OrphaNet|HSDN C0009398 Color vision defects C0007786 Brain ischemia HSDN C2032396 Pelvic pain on the right C2936403 46, xx disorders of sex development HSDN C0035229 Respiratory function impaired C1832661 Anophthalmia and pulmonary hypoplasia MalaCards|HPO C1963091 Diarrhea adverse event C0038273 Stereotypic movement disorder HSDN C0007758 Cerebellar ataxia C0036161 Sandhoff disease OrphaNet|HPO C0022346 Yellow skin C0043515 Zollinger-ellison syndrome MalaCards C0522224 Palsied C0560651 Spinal cord syndrome central HSDN C1963252 Tremor adverse event C3714514 Infection HSDN C4085211 Pain distress question C0001623 Adrenal gland hypofunction HSDN C2984057 Have nausea C0006663 Calcinosis HSDN C4084775 Usual severity weight loss C0153463 Malig neop oth spec pancreas MalaCards C1963091 Diarrhea adverse event C1849236 Severe combined immunodeficiency, atypical HPO C3887638 Failure to thrive in infant C2673377 Mucolipidosis ii alpha/beta (disorder) HPO C3898969 Have been vomiting C1865145 Congenital disorder of glycosylation type 1b MalaCards|HPO C2032395 Pelvic pain on the left C0037856 Spermatic cord torsion HSDN C0151311 Cranial nerve palsy C0796274 Brown-vialetto-van laere syndrome OrphaNet|MalaCards C0030794 Pelvis pain C0007527 Cecal disease HSDN C0751401 Ophthalmoparesis C1864233 Endplate acetylcholinesterase deficiency (disorder) MalaCards|HPO|UMLS C0857305 Thrombocytopenia purpura C1553188 Hemolysis - observation HSDN C0033774 Skin pruritus C1335315 Pancreatic serous cystadenocarcinoma UMLS C2032395 Pelvic pain on the left C0041952 Uerterolithiasis HSDN C0027796 Neuralgias C0008350 Cholelithiasis HSDN C2055125 Temperature reported over 102 degrees fahrenheit C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0000737 Abdomen pain C2347126 Microscopic polyarteritis MalaCards C0003862 Pain joint C0524620 Metabolic syndrome x HSDN C0037199 Sinus infection C1863239 Partial adenosine deaminase deficiency HPO C0851578 Disorder sleep C0266836 Infantile colic HSDN C1963137 Hydrocephalus adverse event C0432209 Dyssegmental dysplasia, rolland-desbuquois type MalaCards C0857305 Thrombocytopenia purpura C0020951 Immune complex diseases HSDN C0270948 Neurogenic muscular atrophy C2745948 Hyalinosis, systemic MalaCards C0020438 Hypercalciuria C3150652 Fanconi renotubular syndrome 2 MalaCards|HPO C0026205 Pupillary constriction C0035934 Rubinstein-taybi syndrome HSDN C1950154 Insomnia homeopathic medication C0027404 Narcolepsy MalaCards C1963063 Anorexia adverse event C0220847 C hepatitis virus HSDN C0237326 Defecation pain C0001403 Addison disease OrphaNet C0242936 Center pain C0950123 Inborn genetic disease HSDN C0026826 High muscle tone C0795959 Gomez lopez hernandez syndrome MalaCards C4084725 Usual severity cough C1962986 Glaucoma adverse event HSDN C0018681 Headache, cephalalgia C0009395 Color perception HSDN C0151889 Reflexes tendon increased C1865409 Amyotrophic lateral sclerosis 4, juvenile MalaCards|HPO C0151889 Reflexes tendon increased C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C0030232 Color loss C0034929 Reflex HSDN C0009398 Color vision defects C0520946 Emotional hypersensitivity HSDN C3463815 Feel fatigue C0020649 Hypotension HSDN C0013604 Edematous C0018188 Granuloma HSDN C0522224 Palsied C0042109 Urticaria HSDN C0522224 Palsied C0007177 Cardiac tamponade HSDN C1963087 Constipation adverse event C0162635 Angelman syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0002957 Anger HSDN C0557874 Global developmental delay C2936826 Fumaric aciduria MalaCards|HPO C1963064 Anxiety adverse event C3280358 Wolfram-like syndrome, autosomal dominant OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0009806 Constipate C2217038 Stage iiib colon cancer UMLS C0043094 Weight gain C0264766 Rheumatic mitral stenosis HSDN C3539893 Pelvic pain occurs with intercourse C0019693 Hiv infections HSDN C0023014 Developmental disorder language C0085094 Head injury closed HSDN C4084775 Usual severity weight loss C0014544 Epilepsy HSDN C3539893 Pelvic pain occurs with intercourse C0018199 Granuloma, plasma cell HSDN C3665386 Abnormal vision C1845050 Pigmentary disorder, reticulate, with systemic manifestations HPO C0007758 Cerebellar ataxia C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C0030552 Paralysis partial C0027092 Myopia HSDN C0018772 Deafness C0038160 Staphylococcal infections HSDN C2024878 Cardiovascular surgery result: dyspnea C0016879 Fusobacterium infections HSDN C4084768 Usual severity vomiting C4014516 Diarrhea 7 MalaCards C2024893 Cardiovascular surgery result: fatigue C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C2237041 Shox gene with short stature C2678223 Mental retardation, x-linked, with panhypopituitarism HPO C1963077 Bone pain adverse event C0342642 Autosomal dominant hypophosphatemic rickets OrphaNet|HPO|MalaCards C0002962 Angina C0040213 Chondropathia tuberosa HSDN C0003469 Anxiety disorder C2931168 Hemangiomas, and cutaneous and intracranial vascular deformations MalaCards C4084784 Diarrhea C0027697 Nephritis HSDN C0013428 Painful urination C0162565 Acute intermittent porphyria MalaCards|HPO|UMLS C0014591 Bleeding nose C1845838 Macrothrombocytopenia, x-linked HPO C3641756 Have diarrhea C0039082 Syndrome HSDN C4084774 Have weight loss C0013386 Dyskinesia, drug-induced HSDN C1963170 Hypothermia adverse event C0242966 Systemic inflammatory response syndrome HSDN C3898969 Have been vomiting C0016171 Fistula of intestine, excluding rectum and anus HSDN C0043094 Weight gain C2937421 Prostatic hyperplasia HSDN C3898969 Have been vomiting C0014849 Esophageal and gastric varices HSDN C0042024 Urine incontinence C1855739 Indifference to pain, congenital, autosomal recessive HPO C2024878 Cardiovascular surgery result: dyspnea C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C1963071 Back pain adverse event C0007789 Cerebral palsy HSDN C0029163 Hemorrhage mouth C1963138 Hypertension adverse event HSDN C2032396 Pelvic pain on the right C0041582 Ulcer HSDN C0023012 Delay language C2674949 Chromosome 3q29 deletion syndrome OrphaNet|MalaCards C1962972 Proteinuria adverse event C0037313 Sleep HSDN C0013362 Dysarthrias C0334123 Histiocytosis, lipoid MalaCards C3539895 Pelvic pain occurs with bowel movement C0004275 Attitude health HSDN C2911647 Weight gain adverse event C0027666 Neoplasms, radiation-induced HSDN C2024893 Cardiovascular surgery result: fatigue C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating HSDN C1579931 Depressed - symptom C0001206 Acromegaly OrphaNet|HPO|MalaCards C0030193 Sense of pain C1333441 Adenoid cystic carcinoma of esophagus UMLS C0575081 Abnormal gait C0856123 Myotonia aggravated OrphaNet C0026838 Spasticity muscle C1855126 3-methylglutaconic aciduria type iv OrphaNet|MalaCards C0234146 Absent reflex C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards C0020672 Body temperature decreased C0020544 Renal hypertension HSDN C1963071 Back pain adverse event C2706915 Language:-:point in time:^patient:- HSDN C0877492 Raw tongue C0017675 Glossitis UMLS C0023380 Lethargy C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO C0085636 Light sensitivity C1138434 Disease, x-linked genetic HSDN C0423735 Tenesmus, urinary vesical C0005686 Urinary bladder diseases UMLS C0344315 Mood depressed C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C1963091 Diarrhea adverse event C1552962 Units of measure - pica HSDN C0042940 Disorder of voice C0029897 Otorhinolaryngologic neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018235 Aggrieved HSDN C0221263 Cafe au lait spot C0037274 Dermatologic disorders HSDN C0018772 Deafness C1306710 Facial asymmetry HSDN C0424755 Fever symptoms C0543697 Mixed cryoglobulinemia OrphaNet|MalaCards C0242936 Center pain C0877792 Sleep disorders, circadian rhythm HSDN C4084766 Vomiting C1856113 Mowat-wilson syndrome MalaCards|HPO C0031911 Pigment deposition C0343115 Skin mastocytoma MalaCards C4085661 Usual severity nausea C0013473 Eating disorders HSDN C2242996 Tingling C0001206 Acromegaly OrphaNet|HSDN|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0085096 Peripheral vascular diseases HSDN C0024312 Lymphocytopenia C2675526 Neutropenia, severe congenital, autosomal recessive 4 HPO C0015672 Decreased energy C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C3539890 Pelvic pain causes awakening at night C0004275 Attitude health HSDN C0030193 Sense of pain C1963120 Gynecomastia adverse event HSDN C0034933 Abnormal reflexes C0034885 Rectal neoplasms HSDN C0043068 Friderichsen-waterhouse syndrome C0041466 Typhoid fever HSDN C0518090 Frequency of pain question C0038531 Subclavian artery stenosis HSDN C0013456 Pain ear C2718092 Acrospiroma HSDN C0036572 Convulsion C0001721 Emotional affect HSDN C0011991 Loose stools C0007570 Celiac disease DiseaseOntology|UMLS C0036572 Convulsion C2751855 Hypomyelination, global cerebral HPO|UMLS C4085862 Bothered by nausea C0014544 Epilepsy HSDN C0026821 Cramp C0238265 Encephalopathy, callosal demyelinating HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017400 Behavioral genetics HSDN C0029163 Hemorrhage mouth C0022361 Jaw cysts HSDN C0237849 Skin desquamation C1260961 Lipoatrophia semicircularis MalaCards C0037315 Breathing disorder during sleeping C0004903 Beckwith-wiedemann syndrome MalaCards C0018681 Headache, cephalalgia C0035127 Cumulative trauma disorders HSDN C0026838 Spasticity muscle C0003493 Aortic diseases HSDN C0270948 Neurogenic muscular atrophy C2930955 Congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy MalaCards C0020615 Hypoglycemia nos C0025267 Multiple endocrine neoplasia type 1 HPO C0851578 Disorder sleep C0042134 Uterine hemorrhage HSDN C4084774 Have weight loss C0007138 Carcinoma, transitional cell HSDN C0010520 Skin cyanosis C0005586 Bipolar disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0037942 Spinal osteophytosis HSDN C4084776 Weight loss C1509147 Histiocytoma HSDN C0030552 Paralysis partial C0010346 Crohn disease HSDN C0001825 Agraphia C0038522 Subacute sclerosing panencephalitis HSDN C0012833 Dizzy C0032962 Pregnancy complications HSDN C4085661 Usual severity nausea C1856401 Etfa deficiencies HPO C0277959 Hair coarseness C2931762 Acrofacial dysostosis, catania type MalaCards C0234132 Pyramidal sign C1854467 Spastic paraplegia 13, autosomal dominant MalaCards|UMLS C0007398 Catatonic C0025235 Melkersson-rosenthal syndrome HSDN C0026838 Spasticity muscle C0029408 Degenerative polyarthritis HSDN C0700590 Diaphoresis excessive C0265334 Pachyonychia congenita OrphaNet|HPO|MalaCards C0037384 Snore C0038454 Cerebrovascular accident HSDN C4084767 Bothered by vomiting C3814778 Hemolytic index HSDN C0015402 Hemorrhage eye C0085270 Orbit pseudotumor HSDN C3665347 Vision impaired C0812437 Oculo-dento-digital syndrome OrphaNet|HPO|MalaCards C4085661 Usual severity nausea C0042331 Migraine variant MalaCards C1963137 Hydrocephalus adverse event C2698658 Orofaciodigital syndrome type 1 MalaCards C0012833 Dizzy C0026771 Trauma multiple HSDN C0040264 Ear ringing sound C0018944 Hematoma HSDN C0424755 Fever symptoms C0153042 Herpetic whitlow DiseaseOntology|MalaCards C0557874 Global developmental delay C1853215 Autosomal recessive frontotemporal pachygyria OrphaNet|MalaCards C0040264 Ear ringing sound C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2203646 Jaundice C0041755 Adverse reaction to drug HSDN C0011991 Loose stools C0497573 Condylomata acuminata in women HSDN C0557874 Global developmental delay C2750748 Chromosome 17p13.3 duplication syndrome OrphaNet|HPO|MalaCards C0575081 Abnormal gait C0334123 Histiocytosis, lipoid MalaCards C1963137 Hydrocephalus adverse event C1857471 Complex of anomalies involving the cranium and brain OrphaNet|MalaCards C2984057 Have nausea C2984299 Asthma pathway HSDN C0003811 Cardiac rhythm disturbance C0751039 Cockayne syndrome, type i HPO C0221232 Welts C0272205 Reactive mastocytosis UMLS C2984057 Have nausea C0017536 Giardiasis DiseaseOntology|HSDN C0026838 Spasticity muscle C2931905 Olivopontocerebellar atrophy 3 MalaCards C0042963 Symptoms vomiting C0000814 Abortion, missed HSDN C4085317 Diarrhea frequency C3541306 Plasmodium measurement HSDN C0271215 Blindness legal C0036202 Sarcoidosis MalaCards|HPO C4084784 Diarrhea C0037926 Compression of spinal cord HSDN C0751837 Gait ataxic C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C3887638 Failure to thrive in infant C1963090 Dehydration adverse event HSDN C4084802 Usual severity diarrhea C0007117 Basal cell carcinoma HSDN C1384666 Decreased hearing C0037304 Skull fracture HSDN C0027497 Queasy C0013292 Obstruction duodenal HSDN C0009806 Constipate C0338503 Septo-optic dysplasia HPO C0035229 Respiratory function impaired C0239849 Harlequin fetus HPO C0000737 Abdomen pain C0003952 Ascaridiasis HSDN C0040034 Thrombocytopenia C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0023530 Leukopenia C1859537 Bare lymphocyte syndrome, type ii, complementation group d HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0022373 Disease, jejunal HSDN C0042571 Vertigo subjective C0524812 Intracranial hypotension HSDN C4084769 Vomiting frequency C0033871 Psychiatric status rating scales HSDN C3641756 Have diarrhea C0205788 Histiocytoid hemangioma HSDN C0243026 Generalized infection C3543867 Collodion fetus MalaCards C0018681 Headache, cephalalgia C0162739 Hellp syndrome HSDN C4085549 Dizziness C1963229 Retinal detachment adverse event HSDN C4084775 Usual severity weight loss C0023903 Liver neoplasms MalaCards C0027769 Tension nervous C0040156 Thyrotoxicosis MalaCards C0015230 Exanthem C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0034124 Pupillary disorder C0011263 Multi-infarct dementia HSDN C4085211 Pain distress question C0022578 Keratoconus HSDN C0518090 Frequency of pain question C0013595 Eczema HSDN C0042420 Vasovagal episode C0007194 Hypertrophic cardiomyopathy HSDN C4084724 Usual severity constipation C0039145 Syringomyelia and syringobulbia HSDN C0860603 Anxiety symptom C1832903 Migraine, sporadic hemiplegic HPO C1963281 Vomiting adverse event C1090821 Sepsis (invertebrate) HSDN C2032395 Pelvic pain on the left C0012979 Canine disease HSDN C0013362 Dysarthrias C1864233 Endplate acetylcholinesterase deficiency (disorder) MalaCards|HPO C0007859 Pain neck C0014474 Ependymoma HSDN C0022346 Yellow skin C0270210 Lucey-driscoll syndrome (disorder) HPO C0025323 Bleeding menstrual heavy C0040015 Thrombasthenia MalaCards|HPO C0018991 Paralysis one side of body C0836924 Thrombocytosis HSDN C1263846 Attention deficit disorder with hyperactivity C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0002963 Angina variant C0024121 Lung neoplasms HSDN C1961131 Cough adverse event C0008628 Chromosome deletion HSDN C0917816 Deficiency mental C1849435 Bicarbonate-wasting rta OrphaNet|HPO C0036396 Sciatica C0034931 Reflex sympathetic dystrophy HSDN C0349588 Stature short C1844887 Catel manzke syndrome OrphaNet|HPO|MalaCards C0009676 Confusion state C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C0151889 Reflexes tendon increased C0282577 Congenital disorders of glycosylation MalaCards C0009421 Comatose C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0857305 Thrombocytopenia purpura C1415369 Gulop gene HSDN C0018808 Murmur C0041409 Turner syndrome, male HSDN C0036572 Convulsion C1863616 Acromelic frontonasal dysostosis MalaCards|HPO|UMLS C0232431 Cold sweat C0001882 Air sickness UMLS C0151786 Weakness muscle C0007795 Diffuse cerebral sclerosis of schilder HSDN C0037383 Sneeze C0005745 Blepharoptosis HSDN C1549543 Administration method - pain C0032226 Pleural diseases HSDN C0424755 Fever symptoms C0021295 Infant, premature, diseases HSDN C0018777 Deafness, conductive C2930867 Inherited congenital bilateral atresia of the external auditory canal, congenital bilateral vertical talus and increased interocular distance MalaCards C0917816 Deficiency mental C0795914 Crome syndrome OrphaNet|MalaCards C1962972 Proteinuria adverse event C0343206 Hypocomplementemic urticarial vasculitis MalaCards C1549543 Administration method - pain C0025209 Melanosis HSDN C0015468 Face pain C0017178 Gastrointestinal diseases HSDN C0008031 Pain chest C2717907 Isolated noncompaction of the ventricular myocardium HSDN C2984058 Have pain C0276926 Schistosoma hematobium infection HSDN C0028961 Urine output decreased C0007097 Carcinomas HSDN C0018991 Paralysis one side of body C0344435 Ventricular fibrillation by ecg finding HSDN C4084725 Usual severity cough C0035435 Rheumatism HSDN C0042384 Vasculitis, nonspecific C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0020673 Hypothermia (central) (local) C1837371 Sudden infant death with dysgenesis of the testes syndrome OrphaNet|HPO|MalaCards C0023015 Language handicap C0037020 Shyness HSDN C0030193 Sense of pain C0008350 Cholelithiasis HSDN C0239376 Lower extremity pain C0684249 Carcinoma of lung UMLS C0039870 Leanness C0007820 Cerebrovascular disorders HSDN C0003862 Pain joint C0043145 Whiplash HSDN C0006370 Bulimia C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0018681 Headache, cephalalgia C0525045 Mood disorders HSDN C0030200 Intractable pain C0027659 Neoplasms, experimental HSDN C0220982 Keto acidosis C3809553 Mitochondrial complex iii deficiency, nuclear type 6 MalaCards C4084788 Have dizziness C0024841 Matrimony, matrimonial HSDN C0030552 Paralysis partial C1864840 Combined oxidative phosphorylation deficiency 3 MalaCards|HPO C0151827 Pain eye C0042487 Venous thrombosis HSDN C0010520 Skin cyanosis C0235833 Congenital diaphragmatic hernia HSDN C3641756 Have diarrhea C0027145 Myxedema HSDN C3641756 Have diarrhea C0020627 Hypopharyngeal neoplasms HSDN C0857305 Thrombocytopenia purpura C0008625 Chromosome aberrations HSDN C0027497 Queasy C0031046 Pericarditis HSDN C0012569 Double vision C0038868 Progressive supranuclear palsy HPO C0020615 Hypoglycemia nos C0024620 Primary malignant neoplasm of liver MalaCards C0018965 Blood urine C0795902 Coloboma, cleft lip-palate and mental retardation syndrome OrphaNet|HPO|MalaCards C1963249 Tinnitus adverse event C1136042 Neuroma, acoustic, bilateral HPO C0023012 Delay language C1853215 Autosomal recessive frontotemporal pachygyria OrphaNet|MalaCards C0040259 Tinea pedis C0006840 Candidiasis HSDN C0022346 Yellow skin C3273069 Bile duct mucinous cystic neoplasm with low grade intraepithelial neoplasia UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0038034 Beurmann disease HSDN C0037383 Sneeze C1999266 Depression adverse event HSDN C0231528 Muscle pain generalized C0549143 Pulmonary renal syndrome MalaCards C0030552 Paralysis partial C0018133 Graft-vs-host disease HSDN C0042024 Urine incontinence C0039231 Tachycardia HSDN C1963184 Nystagmus adverse event C1857682 Combined oxidative phosphorylation deficiency 4 MalaCards|HPO C2911645 Weight loss adverse event C0004659 Bacteriuria HSDN C0022346 Yellow skin C3273032 Lymphoepithelioma-like hepatocellular carcinoma UMLS C2919142 Short stature adverse event C0026363 Mohr-claussen syndrome MalaCards C0460137 Push down or depress C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C1549543 Administration method - pain C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C0038002 Spleen enlargement C0085132 Mucopolysaccharidosis vii OrphaNet|HPO C0231678 Ulnar deviation of the wrists C1862472 Oculomelic amyoplasia MalaCards C0557874 Global developmental delay C1865349 Ethylmalonic encephalopathy HPO C0026838 Spasticity muscle C1852372 Mitochondrial complex iii deficiency (disorder) HPO C4084727 Cough frequency C0867389 Chronic graft-versus-host disease MalaCards C0349588 Stature short C0265493 Cat eye syndrome OrphaNet|MalaCards C1959629 Seizure adverse event C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) MalaCards C0018784 Deafness sensorineural C4014942 Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia MalaCards C0027796 Neuralgias C0024636 Malocclusion HSDN C2984058 Have pain C0004099 Asthma, exercise-induced HSDN C0004134 Dyssynergia C0796222 Mental retardation, x linked 16 MalaCards|HPO C0015469 Facial paralysis C2931811 Chromosome 18, trisomy 18p MalaCards C0005745 Blepharoptosis C3280296 Microcephaly-capillary malformation syndrome MalaCards C0009421 Comatose C0017181 Gastrointestinal hemorrhage HSDN C1069915 Vertigo C0000768 Congenital abnormality HSDN C0004134 Dyssynergia C1849409 Knobloch syndrome HPO C2032395 Pelvic pain on the left C2911643 Encounter due to family history of osteoporosis HSDN C4085210 Usual severity pain C0017152 Gastritis HSDN C4084723 Constipation C0948089 Acute coronary syndrome HSDN C0013595 Eczematous dermatitis C0013575 Ectodermal dysplasia MalaCards C0234146 Absent reflex C0043116 Hmn (hereditary motor neuropathy) proximal type i HPO C0271234 Low vision, both eyes unspec. C0271216 Impairment level of both eyes, nos UMLS C2315100 Pediatric failure to thrive C1968602 Surfactant metabolism dysfunction, pulmonary, 1 MalaCards|HPO C0002622 Amnesias C0349464 Wernicke-korsakoff syndrome HSDN C2984058 Have pain C0015814 Femur head necrosis HSDN C0149793 Transient monocular blindness C0011263 Multi-infarct dementia HSDN C2984058 Have pain C0033839 Pseudorabies HSDN C0011991 Loose stools C0001727 Afferent loop syndrome HSDN C0149651 Clubbing C0345893 Juvenile polyposis syndrome HPO C0085636 Light sensitivity C0037274 Dermatologic disorders HSDN C4084775 Usual severity weight loss C0850803 Anaphylaxis (non medication) HSDN C1963090 Dehydration adverse event C0015624 Fanconi syndrome HPO C0007758 Cerebellar ataxia C0014661 Equine infectious anemia HSDN C0002965 Crescendo angina C0042870 Vitamin d deficiency HSDN C2315100 Pediatric failure to thrive C3809691 Short-rib thoracic dysplasia 8 with or without polydactyly MalaCards C0497247 Blood pressure elevation C0700095 Central neuroblastoma MalaCards C0040822 D tremors C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards|HPO C0035078 Failure kidney C3149841 Polycystic kidney disease 1 HPO C0020580 Decreased sensation C0085648 Synovial cyst HSDN C0027497 Queasy C0023448 Lymphoid leukemia HSDN C1963184 Nystagmus adverse event C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C0027497 Queasy C0600260 Lung diseases, obstructive HSDN C0040264 Ear ringing sound C0002726 Amyloidosis HSDN C0018772 Deafness C0002736 Amyotrophic lateral sclerosis HSDN C1963091 Diarrhea adverse event C1510428 Cerebral abscess HSDN C0234146 Absent reflex C0685838 Gonadal dysgenesis xx type deafness MalaCards|HPO C0522224 Palsied C0042373 Vascular diseases HSDN C0028738 Nystagmus C2680447 Spg45 gene HPO C0015672 Decreased energy C0035222 Respiratory distress syndrome, adult HSDN C0019209 Large liver C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0011991 Loose stools C0003838 Arterial occlusive diseases HSDN C0036572 Convulsion C0023092 Lassa fever MalaCards C0458002 Acquired dysphasias C0454560 Acquired language disorder UMLS C1963177 Muscle pain adverse event C0221055 Paramyotonia congenita (disorder) MalaCards C4085210 Usual severity pain C0162869 Aneurysm, ruptured HSDN C0017181 Gastrointestinal bleed C1848029 Ehlers-danlos syndrome caused by tenascin-x deficiency HPO C0039870 Leanness C0033975 Psychotic disorders HSDN C4084769 Vomiting frequency C1856113 Mowat-wilson syndrome MalaCards|HPO C4085549 Dizziness C3714514 Infection HSDN C0030552 Paralysis partial C0036983 Septic shock HSDN C4020887 Photodysphoria C2750065 Retinitis pigmentosa, juvenile, lrat-related HPO C1963249 Tinnitus adverse event C0002895 Anemia, sickle cell HSDN C0015672 Decreased energy C0035335 Retinoblastoma HSDN C0015468 Face pain C0022661 Kidney failure, chronic HSDN C4084727 Cough frequency C0339946 Pulmonary tularemia DiseaseOntology|MalaCards C0036572 Convulsion C1962979 Burn adverse event HSDN C4084776 Weight loss C0854359 Autoimmune endocrine disease insulin syndrome OrphaNet|MalaCards C0018777 Deafness, conductive C1302282 Chromaffin cell neoplasm MalaCards C4085549 Dizziness C4049644 Depression HSDN C0015672 Decreased energy C0079027 Blood loss, surgical HSDN C0751837 Gait ataxic C1845366 Mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance MalaCards|HPO|UMLS C4084775 Usual severity weight loss C0022661 Kidney failure, chronic HSDN C3641755 Have constipation C1546635 Specimen source codes - fistula HSDN C4085210 Usual severity pain C0014145 Yolk sac tumor HSDN C0030552 Paralysis partial C0040046 Thrombophlebitis HSDN C0917801 Sleep disorder insomnia C0028756 Obesity, morbid UMLS C0019079 Bloody sputum C1336175 Stage iib adenosquamous cell carcinoma of lung UMLS C4084767 Bothered by vomiting C2713347 7-dehydrocholesterol reductase deficiency MalaCards C0033377 Caudal displacement C1838180 Codas syndrome OrphaNet|HPO|MalaCards C0015970 Fever unknown origin C1458155 Mammary neoplasms HSDN C0030193 Sense of pain C0001969 Alcoholic intoxication HSDN C1565249 Limitation, mobility C0029434 Osteogenesis imperfecta HSDN C1959630 Eye pain adverse event C0017601 Glaucomas HSDN C2911647 Weight gain adverse event C0040435 Tooth diseases HSDN C0039070 Collapse fleeting C0042345 Varicosity HSDN C4084774 Have weight loss C3541994 Drug hypersensitivity syndrome OrphaNet|MalaCards C0015230 Exanthem C0392439 Acrodermatitis continua of hallopeau UMLS C0577567 Mass of urogenital structure C0564715 Benign genital neoplasm UMLS C0018681 Headache, cephalalgia C0702221 Tactual discrimination HSDN C2237041 Shox gene with short stature C0268496 Kramer syndrome OrphaNet|MalaCards C0018681 Headache, cephalalgia C0035869 Rotavirus infections HSDN C3274924 Have been coughing C0085232 Diverticulum zenker HSDN C0014591 Bleeding nose C2717750 Platelet alpha-granule deficiency MalaCards C0033377 Caudal displacement C2931928 Mitochondrial cytopathy MalaCards C0036572 Convulsion C3662855 Partial frontal lobe epilepsy UMLS C0241165 Skin thickening C0086431 Hurler-scheie syndrome UMLS C2984058 Have pain C0206704 Carcinoma, large cell HSDN C2096293 Ent surgical result ear vertigo C0796561 Melanoma vaccines HSDN C2029884 Hearing loss by exam C0078981 Arachnoid cysts HSDN C0234471 Conduction aphasia C0033923 Psychomotor function HSDN C0013132 Drooling C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) HPO C0011991 Loose stools C1866495 Bartter syndrome, antenatal type 1 HPO|UMLS C0025222 Black stool C0043194 Wiskott-aldrich syndrome MalaCards C0000737 Abdomen pain C0040128 Thyroid diseases HSDN C0013421 Dystonia C1556061 Electric injuries HSDN C1549543 Administration method - pain C0027658 Neoplasms, germ cell and embryonal HSDN C3274924 Have been coughing C0039978 Thoracic diseases HSDN C1963281 Vomiting adverse event C0024121 Lung neoplasms HSDN C0018784 Deafness sensorineural C0796173 Spondyloperipheral dysplasia short ulna MalaCards|HPO C0031911 Pigment deposition C3541517 Ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant MalaCards C4084742 Bothered by night sweats C0023281 Leishmaniasis OrphaNet|MalaCards C0022107 Fussiness C0268412 Infantile hypophosphatasia MalaCards|HPO C4085211 Pain distress question C0344423 Atrial flutter by ecg finding HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0028796 Dermatitis, occupational HSDN C4085211 Pain distress question C2355609 Mycetoma of foot HSDN C0026826 High muscle tone C0026847 Spinal muscular atrophy HSDN C0007814 Cerebrospinal fluid otorrhea C0018946 Hematoma, subdural HSDN C2237041 Shox gene with short stature C3280355 Chromosome 15q25 deletion syndrome MalaCards C0036572 Convulsion C0027344 Nails, malformed HSDN C1963091 Diarrhea adverse event C0236736 Cocaine-related disorders HSDN C0020538 Hbp C0751039 Cockayne syndrome, type i HPO C3274924 Have been coughing C0009373 Colonic diseases HSDN C3898969 Have been vomiting C0018946 Hematoma, subdural HSDN C0009806 Constipate C0004933 Behavior modification technique HSDN C0030193 Sense of pain C0279697 Epidermoid carcinoma, salivary gland UMLS C1838869 Proximal neurogenic muscle weakness C4015624 Myopathy, vacuolar, with casq1 aggregates MalaCards C0038868 Supranuclear palsy progressive C0087012 Ataxia, spinocerebellar HSDN C0086565 Liver function abnormal C2748941 Glycogen storage disease, type ixa2 HPO C0036572 Convulsion C1836915 Mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature UMLS C0030552 Paralysis partial C0162809 Kallmann syndrome MalaCards|HPO C1963087 Constipation adverse event C0009324 Ulcerative colitis HSDN C1557397 Adverse event associated with pain C0339143 Thyroid associated opthalmopathies HSDN C0332573 Macula C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0024032 Birth weight subnormal C0015934 Fetal growth retardation MalaCards C4085548 Usual severity dizziness C1704436 Peripheral arterial diseases HSDN C3146279 Coma C0001940 Alcohol amnestic disorder HSDN C0012833 Dizzy C0033860 Psoriasis HSDN C0008031 Pain chest C0026785 Munchhausen syndrome HSDN C0015230 Exanthem C0263605 Polymorphous light eruption, diffuse erythematous type UMLS C3898969 Have been vomiting C0009187 Coccidiosis HSDN C4084724 Usual severity constipation C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C4085210 Usual severity pain C0019021 Hemoglobin c disease HSDN C3829611 Nausea frequency C0036202 Sarcoidosis HSDN C0522224 Palsied C0038941 Incisional infection HSDN C0349588 Stature short C1842679 Thai symphalangism syndrome MalaCards C1384666 Decreased hearing C2677515 Otosclerosis 8 (disorder) MalaCards C0040822 D tremors C0026847 Spinal muscular atrophy HSDN C0206160 Retic count elevated C1856143 Hemolytic uremic syndrome, typical MalaCards C1963071 Back pain adverse event C0035358 Retroperitoneal neoplasm HSDN C1963091 Diarrhea adverse event C0023869 Lithiasis HSDN C0042024 Urine incontinence C0032019 Pituitary neoplasms HSDN C0522224 Palsied C1546654 Specimen source codes - granuloma HSDN C4084775 Usual severity weight loss C0032787 Postoperative complications HSDN C2024878 Cardiovascular surgery result: dyspnea C0017638 Glioma HSDN C0011991 Loose stools C0013922 Embolism HSDN C3815497 Cough C0000768 Congenital abnormality HSDN C2919142 Short stature adverse event C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C3541349 Syncope C0009450 Disease caused by microorganism HSDN C3898969 Have been vomiting C3495559 Juvenile arthritis HSDN C0003126 Smell loss C0338503 Septo-optic dysplasia HPO C0020458 Hyperhydrosis C1861457 Progressive encephalomyelitis with rigidity MalaCards C0231528 Muscle pain generalized C3536827 Glycogenosis with glucoaminophosphaturia MalaCards C3829611 Nausea frequency C1260386 Glucocorticoid-remediable aldosteronism HPO C0424755 Fever symptoms C0001618 Tumors of adrenal cortex HSDN C0042940 Disorder of voice C0206636 Chondromatosis HSDN C0237326 Defecation pain C0085655 Polymyositis OrphaNet|MalaCards C4085210 Usual severity pain C0517960 Neurological status: consciousness HSDN C0041667 Low weight C3550904 Epileptic encephalopathy, early infantile, 36 MalaCards C3815497 Cough C0038160 Staphylococcal infections HSDN C3665492 Pigmentations C0030354 Papilloma MalaCards C0184567 Pain acute C0008475 Patella chondromalacia HSDN C0023015 Language handicap C0175754 Agenesis of corpus callosum HSDN C0241210 Speaking delay C0795953 Masa syndrome (disorder) OrphaNet|HPO|MalaCards C0015300 Ocular proptosis C0795940 Filippi syndrome MalaCards|HPO C0518090 Frequency of pain question C0025209 Melanosis HSDN C1549543 Administration method - pain C0039520 Tenosynovitis HSDN C0040034 Thrombocytopenia C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C3551954 Coenzyme q10 deficiency, primary, 1 MalaCards|UMLS C0009460 Communication impairment C0009240 Cognition HSDN C0026838 Spasticity muscle C0021171 Bloch sulzberger syndrome MalaCards|HPO|UMLS C4084726 Distress cough C0023448 Lymphoid leukemia HSDN C0522224 Palsied C0028433 Nose neoplasms HSDN C1962972 Proteinuria adverse event C0004153 Atherosclerosis HSDN C1549543 Administration method - pain C0015404 Eye infections, bacterial HSDN C4084766 Vomiting C0021828 Intestinal atresia HSDN C0557874 Global developmental delay C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C1963091 Diarrhea adverse event C0022373 Disease, jejunal HSDN C0040034 Thrombocytopenia C0342288 Insulin-dependent diabetes mellitus secretory diarrhea syndrome MalaCards|HPO C3649123 Feared medical condition with no diagnosis made C0233403 Physically well but worried UMLS C2364111 Gustatory anesthesia C0025295 Meningitis, pneumococcal HSDN C4084773 Bothered by weight gain C0020541 Hypertension, portal HSDN C0023380 Lethargy C0005866 Bluetongue HSDN C0030486 Extremity paralysis, lower C0025202 Melanoma HSDN C0858971 Ventilation difficult C3203358 Hypoventilation UMLS C3539893 Pelvic pain occurs with intercourse C0014179 Endometritis HSDN C0020673 Hypothermia (central) (local) C0042769 Virus diseases HSDN C0010038 Corneal opacity disorder C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards C0000737 Abdomen pain C0039494 Temporomandibular joint disorders HSDN C0424755 Fever symptoms C0016663 Pathological fracture HSDN C4084727 Cough frequency C0006271 Bronchiolitis MalaCards C1000483 Genus anemia C0268496 Kramer syndrome OrphaNet|MalaCards C1838869 Proximal neurogenic muscle weakness C1834558 Myopathy, centronuclear, autosomal dominant HPO C0019209 Large liver C0220710 Medium-chain acyl-coenzyme a dehydrogenase deficiency HPO C0009806 Constipate C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C0344487 Lateral meningocele MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027051 Myocardial infarction HSDN C0027796 Neuralgias C0029456 Osteoporosis HSDN C0018991 Paralysis one side of body C1962976 Ventricular fibrillation adverse event HSDN C0036572 Convulsion C0007787 Transient ischemic attack HSDN C4084768 Usual severity vomiting C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0018681 Headache, cephalalgia C1866398 Proteus-like syndrome (disorder) MalaCards C0034150 Skin purpura C0041948 Uremia HSDN C2024878 Cardiovascular surgery result: dyspnea C1546847 Entity name part type - family HSDN C1069915 Vertigo C0752160 Hemangioma, cavernous, central nervous system HSDN C0008031 Pain chest C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C1145670 Failure respiratory C2930962 Fried goldberg mundel syndrome OrphaNet C1999266 Depression adverse event C0242526 Gonadal dysgenesis, 45,x MalaCards C0025287 Meningitis-like C0006114 Cerebral edema HSDN C1384666 Decreased hearing C0036202 Sarcoidosis HSDN C0026838 Spasticity muscle C3714514 Infection HSDN C4085210 Usual severity pain C0022610 Kernicterus HSDN C0151786 Weakness muscle C0010267 Cranial nerve neoplasms HSDN C0011206 Delirium acute C0003486 Aortic aneurysm HSDN C0022346 Yellow skin C0013902 Elliptocytosis, hereditary HSDN C0007758 Cerebellar ataxia C0221065 Subacute combined degeneration HSDN C0009460 Communication impairment C0007820 Cerebrovascular disorders HSDN C0026838 Spasticity muscle C2026475 Monoplegic cerebral palsy with spasticity UMLS C0042024 Urine incontinence C1849722 Polyglucosan body disease, adult form OrphaNet|HPO|MalaCards C0030200 Intractable pain C0031511 Pheochromocytoma HSDN C0027497 Queasy C0006145 Breast diseases HSDN C0460137 Push down or depress C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0232466 Feeding difficulty C3276432 Multiple mitochondrial dysfunctions syndrome 1 MalaCards C0497406 Over weight C0021831 Intestinal diseases HSDN C4085317 Diarrhea frequency C0035012 Reiter syndrome OrphaNet|MalaCards C0026838 Spasticity muscle C0268141 Xeroderma pigmentosum, group g HPO C0848203 Male pelvic pain C0009450 Disease caused by microorganism HSDN C0042798 Vision dim C1844777 Cone dystrophy, x-linked, 1 MalaCards|HPO C0042963 Symptoms vomiting C0017574 Gingivitis HSDN C4085317 Diarrhea frequency C0002726 Amyloidosis HSDN C4084784 Diarrhea C0022593 Keratosis HSDN C0022107 Fussiness C0005283 Beta thalassemia OrphaNet C0013404 Respiratory difficulty C0744971 Hiv lymphadenopathy UMLS C0234132 Pyramidal sign C0393590 Fahr's syndrome (disorder) MalaCards|HPO C0003811 Cardiac rhythm disturbance C0878677 Glycogen storage disease type iib MalaCards|HPO C0427008 Stiffness C3539013 Aicardi-goutieres syndrome 6 MalaCards|UMLS C0018784 Deafness sensorineural C0034063 Pulmonary edema HSDN C0009398 Color vision defects C1963064 Anxiety adverse event HSDN C0518090 Frequency of pain question C0008412 Choline deficiency HSDN C4084775 Usual severity weight loss C0029928 Ovarian diseases HSDN C1963137 Hydrocephalus adverse event C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C4085211 Pain distress question C0041601 Ulna fracture HSDN C4084769 Vomiting frequency C0032229 Pleural neoplasms HSDN C4084784 Diarrhea C0149778 Soft tissue infections HSDN C4084724 Usual severity constipation C0080174 Spina bifida occulta HSDN C0577569 Mass of male genital structure C0347179 Ca-in-situ male genital nos UMLS C3815497 Cough C0002736 Amyotrophic lateral sclerosis HSDN C1963091 Diarrhea adverse event C0008519 Ectopic tissue HSDN C0242936 Center pain C0860239 Catheter infections related HSDN C0700078 Deep tendon reflex decrease C0011195 Dejerine-sottas disease (disorder) HPO C0036572 Convulsion C0036503 Sebaceous gland neoplasms HSDN C0009421 Comatose C0007795 Diffuse cerebral sclerosis of schilder HSDN C2029884 Hearing loss by exam C0919267 Ovarian neoplasm HSDN C4085661 Usual severity nausea C0206715 Neoplasms, neuroepithelial HSDN C0042024 Urine incontinence C0024228 Lymphatic diseases HSDN C0242936 Center pain C2350529 Pulmonary aspergillosis HSDN C0085636 Light sensitivity C1842914 Adult-onset vitelliform macular dystrophy MalaCards|HPO|UMLS C4084784 Diarrhea C0037650 Somatoform disorder HSDN C0007859 Pain neck C0085083 Ovarian hyperstimulation syndrome HSDN C4084802 Usual severity diarrhea C3658208 Disbioses HSDN C1557397 Adverse event associated with pain C0036221 Mast-cell sarcoma HSDN C0018772 Deafness C0585442 Osteosarcoma of bone HSDN C3539896 Pelvic pain occurs with urination C0022410 Joint instability HSDN C0018777 Deafness, conductive C1848864 Thoracic dysplasia-hydrocephalus syndrome OrphaNet|MalaCards C0036572 Convulsion C1859312 Camfak syndrome OrphaNet|HPO C3829611 Nausea frequency C0002453 Amenorrhea HSDN C4084725 Usual severity cough C0019829 Hodgkin disease OrphaNet C0150055 Pain chronic C0152054 Therapeutic touch HSDN C0018834 Brash C2936904 Opitz gbbb syndrome, x-linked MalaCards|HPO C0018681 Headache, cephalalgia C0022578 Keratoconus HSDN C0235876 Aggravated depression C0011570 Mental depression UMLS C3887873 Hearing loss C0029401 Osteitis deformans HSDN C4085862 Bothered by nausea C0003507 Aortic valve stenosis HSDN C1963170 Hypothermia adverse event C0026857 Musculoskeletal diseases HSDN C0008031 Pain chest C0348018 Projections HSDN C1963093 Dizziness adverse event C0036439 Scoliosis, unspecified HSDN C2919142 Short stature adverse event C0852654 21-hydroxylase deficiency MalaCards C0033377 Caudal displacement C0796142 Sao paulo mca-mr syndrome MalaCards C0033377 Caudal displacement C0265303 Acrocephalopolysyndactyly type iv OrphaNet|MalaCards C3541349 Syncope C0242698 Ventricular dysfunction, left HSDN C0033377 Caudal displacement C1853623 Fryns-aftimos syndrome MalaCards C0474368 Childbirth pain C0013418 Abnormal labor HSDN C0003862 Pain joint C0031069 Familial mediterranean fever OrphaNet|HPO|UMLS C0018772 Deafness C0432365 Thalidomide embryopathy syndrome MalaCards C0012833 Dizzy C0010068 Coronary heart disease HSDN C3887638 Failure to thrive in infant C0006287 Bronchopulmonary dysplasia HSDN C4084727 Cough frequency C0153416 Malig neop oth spec part oesop MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C0700590 Diaphoresis excessive C1854336 Paragangliomas 3 MalaCards|HPO C4085210 Usual severity pain C0033075 Presbyopia HSDN C0018772 Deafness C0700208 Acquired scoliosis HSDN C1963252 Tremor adverse event C0393571 Multiple system atrophy HSDN C1963281 Vomiting adverse event C0205710 Alpers syndrome (disorder) MalaCards|HPO C0030552 Paralysis partial C1419869 Scnn1b gene HSDN C0023380 Lethargy C2718087 Vitamin k deficiency bleeding HSDN C0004134 Dyssynergia C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C0030193 Sense of pain C0009759 Conjunctival diseases HSDN C0151311 Cranial nerve palsy C0025286 Meningioma MalaCards C0028084 Terrifying dreams C0234458 Dream disorder UMLS C0008031 Pain chest C0271865 Autoimmune hypoparathyroidism MalaCards C4085210 Usual severity pain C0020651 Hypotension, orthostatic HSDN C3274924 Have been coughing C0020538 Hypertensive disease HSDN C4085862 Bothered by nausea C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C1961131 Cough adverse event C3203727 Pneumorrhachi HSDN C1963249 Tinnitus adverse event C0014544 Epilepsy HSDN C0005745 Blepharoptosis C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C0428977 Pulse rate decrease C2751315 Atrial septal defect 6 MalaCards|HPO C0036572 Convulsion C1854988 Molybdenum cofactor deficiency, complementation group a HPO C0011175 Deficient fluid volume C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C1963091 Diarrhea adverse event C0020461 Hyperkalemia HSDN C0000737 Abdomen pain C0850803 Anaphylaxis (non medication) HSDN C1263846 Attention deficit disorder with hyperactivity C1969623 Neurofibromatosis, type 1-like syndrome MalaCards|HPO C0270948 Neurogenic muscular atrophy C1854961 Lisker garcia ramos syndrome MalaCards C0013404 Respiratory difficulty C0854891 Malignant pleural mesothelioma recurrent UMLS C0011168 Disorder deglutition C0796274 Brown-vialetto-van laere syndrome OrphaNet|HPO|MalaCards C2242996 Tingling C0030920 Peptic ulcer HSDN C1963090 Dehydration adverse event C0079583 Ichthyosiform erythroderma, congenital MalaCards C0022346 Yellow skin C0024116 Lung diseases, fungal HSDN C0424755 Fever symptoms C0035592 Infection, rickettsiaceae MalaCards C0015672 Decreased energy C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0557874 Global developmental delay C3280168 Hsn2c MalaCards C0030193 Sense of pain C1510502 Oxyphilic adenoma HSDN C4049602 Hyperactivity C2931246 Chromosome 17, trisomy 17p11 2 MalaCards C0151786 Weakness muscle C0022865 Obstetric labor complications HSDN C0012569 Double vision C0007274 Carotid artery thrombosis HSDN C3463815 Feel fatigue C0237873 Physiological sexual disorders HSDN C0042928 Paralysis vocal cord C0040150 Thyroiditis acute pyogenic HSDN C0030193 Sense of pain C0024693 Mandible injury HSDN C2032396 Pelvic pain on the right C0006118 Brain neoplasms HSDN C0231706 Circling C0027983 Newcastle disease DiseaseOntology|MalaCards C0233794 Memory impaired C0751254 Creutzfeldt-jakob disease, familial MalaCards|HPO C3898969 Have been vomiting C0027686 Pathologic neovascularization HSDN C1963066 Joint pain adverse event C0006309 Brucellosis DiseaseOntology|MalaCards C1963086 Confusion adverse event C3244301 Coverage level - family HSDN C0031911 Pigment deposition C0265325 Turcot syndrome (disorder) MalaCards C0027498 Nausea vomiting C0023896 Alcoholic liver diseases UMLS C0009421 Comatose C0342788 Renal carnitine transport defect MalaCards|HPO C0020649 Blood pressure decreased C0271737 Addison's disease due to autoimmunity OrphaNet C0917816 Deficiency mental C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C0042024 Urine incontinence C0008073 Developmental disabilities HSDN C1000483 Genus anemia C2930815 Acute cerebral gaucher disease MalaCards C2025995 Cellulitis C0022739 Klippel-trenaunay-weber syndrome MalaCards C0018772 Deafness C0001122 Acidosis HSDN C0740426 Tibia pain C0740728 Lower extremity problem UMLS C2919142 Short stature adverse event C0018609 Hartnup disease MalaCards|HPO C4084775 Usual severity weight loss C0041313 Hepatic tuberculosis DiseaseOntology|MalaCards C0030193 Sense of pain C0027436 Nasociliary neuralgia UMLS C4084784 Diarrhea C0024523 Malabsorption syndrome MalaCards C0026826 High muscle tone C3150707 Chromosome 14q11-q22 deletion syndrome MalaCards C4084802 Usual severity diarrhea C0687720 Central diabetes insipidus MalaCards C0349506 Sun sensitivity C0032339 Rothmund-thomson syndrome OrphaNet|HPO|MalaCards C0086437 Joint hypermobility C0016395 Focal dermal hypoplasia MalaCards|HPO|UMLS C0587246 Extremity weakness C1850569 Nemaline myopathy 2 HPO C4084802 Usual severity diarrhea C1705714 Lats1 wt allele HSDN C2024893 Cardiovascular surgery result: fatigue C0023418 Leukemia HSDN C4084774 Have weight loss C1963119 Stomach ulcer adverse event HSDN C0557874 Global developmental delay C1838299 Peroxisome biogenesis disorder, complementation group 14 MalaCards C0015970 Fever unknown origin C0014122 Subacute bacterial endocarditis HSDN C0020458 Hyperhydrosis C1148551 X-linked dyskeratosis congenita MalaCards|HPO C2096293 Ent surgical result ear vertigo C0700208 Acquired scoliosis HSDN C3539022 Pelvic pain decreasing in severity C0016664 Fatigue fracture HSDN C3539020 Pelvic pain decreasing in frequency C0007867 Cervix diseases HSDN C0015970 Fever unknown origin C0038454 Cerebrovascular accident HSDN C1959630 Eye pain adverse event C0008698 Maxillary sinusitis chronic HSDN C0030193 Sense of pain C2355609 Mycetoma of foot HSDN C0018784 Deafness sensorineural C4015436 Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus MalaCards C2128255 Shoulder can be dislocated voluntarily C0432227 Brachyolmia type 3 MalaCards C0042571 Vertigo subjective C0234755 Vertigo, ocular UMLS C0034150 Skin purpura C0010709 Cyst HSDN C0234146 Absent reflex C3280845 Charcot-marie-tooth disease, dominant intermediate e MalaCards C0011570 Monopolar depression C1862939 Amyotrophic lateral sclerosis 1 MalaCards C4084802 Usual severity diarrhea C0013502 Echinococcosis HSDN C3641756 Have diarrhea C0023448 Lymphoid leukemia HSDN C0031911 Pigment deposition C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0413252 Hypothermia due to exposure C0000833 Abscess HSDN C0018524 Hallucinate C0036341 Schizophrenia MalaCards|HPO C1557397 Adverse event associated with pain C0035459 Atrophic rhinitis HSDN C0030193 Sense of pain C0032310 Pneumonia, viral HSDN C4085548 Usual severity dizziness C0003850 Arteriosclerosis HSDN C1279888 Proteinuria of undiagnosed cause C0043397 Yellow fever, jungle MalaCards C0917816 Deficiency mental C1135161 Stage 4s neuroblastoma MalaCards C0012833 Dizzy C1834559 Continuous muscle fiber activity, hereditary HPO C0518090 Frequency of pain question C0242666 Protein s deficiency HSDN C4084774 Have weight loss C0043325 Xanthomatosis HSDN C0018681 Headache, cephalalgia C1334646 Maxillary sinus schneiderian papilloma UMLS C1549543 Administration method - pain C0282687 Hemorrhagic fever, ebola HSDN C1519353 Skin eruption papular C0406555 Elastoderma OrphaNet|MalaCards C4084726 Distress cough C0233629 Thinking and speaking disturbances HSDN C4084767 Bothered by vomiting C0036216 Sarcoma, experimental HSDN C0344434 Atrial fibrillation ecg C3151265 Cardiomyopathy, familial hypertrophic, 18 HPO C4084802 Usual severity diarrhea C0027430 Nasal polyps HSDN C0026821 Cramp C0040046 Thrombophlebitis HSDN C4084775 Usual severity weight loss C0002949 Aneurysm, dissecting HSDN C4042891 Sleep wake disorders C0684314 Adolescent drinking HSDN C0019209 Large liver C0015938 Fetal macrosomia MalaCards|HSDN C4084766 Vomiting C2746068 Congenital idiopathic intestinal pseudoobstruction HPO C2984058 Have pain C0017920 Glycogen storage disease type i HSDN C0018772 Deafness C0085278 Antiphospholipid syndrome HSDN C0028738 Nystagmus C1865981 Friedreich ataxia 2 MalaCards C4049644 Depression C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C1549543 Administration method - pain C0001075 Achlorhydria HSDN C0018681 Headache, cephalalgia C1322286 Thymoma, type c MalaCards C4084725 Usual severity cough C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C1963252 Tremor adverse event C1956346 Coronary artery disease HSDN C4084726 Distress cough C0003949 Asbestosis HSDN C0010038 Corneal opacity disorder C0030804 Pemphigoid, benign mucous membrane MalaCards C4084776 Weight loss C0281508 Desmoplastic small round cell tumor OrphaNet|MalaCards C0917816 Deficiency mental C0265224 Freeman-sheldon syndrome MalaCards|HPO C0241157 Skin pustule C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome OrphaNet|MalaCards C1384666 Decreased hearing C0003873 Rheumatoid arthritis HSDN C0009806 Constipate C0175713 Aicardi's syndrome MalaCards C4084776 Weight loss C3887532 Ulceration HSDN C0547030 Sensory perceptual alteration: visual C3648212 Late effects of nontraumatic intracranial hemorrhage vision disturbances UMLS C0232462 Appetite decrease C0003175 Anthrax disease MalaCards C0018784 Deafness sensorineural C0305062 Tetanus toxoids HSDN C0151908 Dry skin C0282529 Chondrodysplasia punctata, rhizomelic OrphaNet|MalaCards C0042755 Virilisation C0030568 Parkinsonism, postencephalitic HSDN C0349489 Fetal hypoxia C0022661 Kidney failure, chronic HSDN C2128839 Infantile behavior C2220010 Socially inappropriate behavior UMLS C4085211 Pain distress question C0036631 Seminoma HSDN C4085222 Nausea C0007194 Hypertrophic cardiomyopathy HSDN C0007166 Cardiac output decreased C0023467 Leukemia, myelocytic, acute HSDN C0030193 Sense of pain C0000817 Abortion septic HSDN C0026838 Spasticity muscle C0037315 Sleep apnea syndromes HSDN C0023530 Leukopenia C1420653 Tcn2 gene HPO C4084775 Usual severity weight loss C0014170 Endometrial neoplasms HSDN C0024031 Back pain lower back C2984291 Glioblastoma multiforme pathway HSDN C4085211 Pain distress question C0020621 Hypokalemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0302497 Retrobulbar haemorrhage HSDN C1963184 Nystagmus adverse event C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0027497 Queasy C0035066 Renal artery obstruction HSDN C0000737 Abdomen pain C1518736 Ovarian small cell carcinoma, hypercalcemic type UMLS C0007758 Cerebellar ataxia C0036690 Septicemia HSDN C0034150 Skin purpura C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C3641756 Have diarrhea C0878544 Cardiomyopathies HSDN C0518090 Frequency of pain question C0206693 Medullary carcinoma HSDN C0011206 Delirium acute C0038160 Staphylococcal infections HSDN C0028738 Nystagmus C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C4084768 Usual severity vomiting C0011334 Dental caries HSDN C0009806 Constipate C0020473 Hyperlipidemia HSDN C4084774 Have weight loss C0009375 Colonic neoplasms HSDN C4085222 Nausea C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0235153 Sensory hallucination C0751278 Metachromatic leukodystrophy, infant MalaCards|HPO C0242936 Center pain C0010074 Coronary vessel anomalies HSDN C0022346 Yellow skin C2007059 Osteoclast-like giant cell neoplasm of pancreas UMLS C0027066 Myoclonic jerking C0014550 Epilepsies, myoclonic MalaCards|UMLS C0013604 Edematous C0001828 Agricultural workers' diseases HSDN C4084724 Usual severity constipation C0012242 Digestive system disorders HSDN C0018772 Deafness C0038362 Stomatitis HSDN C3887873 Hearing loss C0035923 German measles vaccine HSDN C2984058 Have pain C0752143 Intracranial thrombosis HSDN C0013404 Respiratory difficulty C0011853 Diabetes mellitus, experimental HSDN C4084768 Usual severity vomiting C0206171 Community acquired infections HSDN C0010038 Corneal opacity disorder C2931648 Larsen syndrome, dominant type MalaCards C0518090 Frequency of pain question C0023891 Liver cirrhosis, alcoholic HSDN C4085661 Usual severity nausea C1532560 Plasmacytoma - category HSDN C3829611 Nausea frequency C1456781 Benign melanocytic nevus HSDN C4085211 Pain distress question C0242666 Protein s deficiency HSDN C4085222 Nausea C0033893 Tension headache HSDN C4085211 Pain distress question C0085409 Polyendocrinopathies, autoimmune HSDN C0013604 Edematous C0014121 Bacterial endocarditis HSDN C0232466 Feeding difficulty C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C0022346 Yellow skin C1518871 Pancreatic intraductal papillary mucinous neoplasm with an associated invasive carcinoma UMLS C0020455 Hypergammaglobulinemia C0023524 Leukoencephalopathy, progressive multifocal HSDN C1963252 Tremor adverse event C0393590 Fahr's syndrome (disorder) MalaCards|HPO C4084724 Usual severity constipation C1443900 Inhalational botulism OrphaNet|MalaCards C4085661 Usual severity nausea C3888013 Hypnoses HSDN C0018777 Deafness, conductive C0410539 Craniodiaphyseal dysplasia OrphaNet|HPO|MalaCards C0013604 Edematous C1509147 Histiocytoma HSDN C0013404 Respiratory difficulty C0041466 Typhoid fever HSDN C0030554 Abnormal sensation C0311375 Arsenic poisoning HSDN C4084725 Usual severity cough C0149725 Lower respiratory tract infection MalaCards C2919142 Short stature adverse event C0220722 Cerebrooculofacioskeletal syndrome 1 OrphaNet|HPO C2984058 Have pain C0003125 Anorexia nervosa HSDN C0454644 Delayed language development C0265216 X-linked hydrocephalus syndrome MalaCards C2911645 Weight loss adverse event C0029463 Osteosarcoma HSDN|HPO C0025287 Meningitis-like C0001486 Adenovirus infections HSDN C0349489 Fetal hypoxia C0020649 Hypotension HSDN C2919142 Short stature adverse event C0175694 Smith-lemli-opitz syndrome OrphaNet|HPO|MalaCards C0151686 Growth retardation C1849554 Lymphangiectasia, pulmonary, congenital OrphaNet|MalaCards C0034150 Skin purpura C0036601 Self mutilation HSDN C0042963 Symptoms vomiting C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C4085222 Nausea C0033873 Psychiatry HSDN C4084776 Weight loss C0006663 Calcinosis HSDN C3641756 Have diarrhea C0039128 Syphilis HSDN C0015970 Fever unknown origin C0020458 Hyperhidrosis disorder HSDN C0013404 Respiratory difficulty C0024003 Lordosis HSDN C0018772 Deafness C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0007758 Cerebellar ataxia C1847725 Spinocerebellar ataxia 15 MalaCards|UMLS C0013421 Dystonia C0085292 Stiff-person syndrome HSDN C0027796 Neuralgias C0003864 Arthritis HSDN C1963091 Diarrhea adverse event C0848377 Trauma to the abdomen HSDN C0242936 Center pain C0017536 Giardiasis HSDN C4084773 Bothered by weight gain C0038587 Substance withdrawal syndrome HSDN C0002965 Crescendo angina C0032285 Pneumonia HSDN C0010520 Skin cyanosis C1849813 Glycogen storage disease of heart, lethal congenital MalaCards|HPO C0018681 Headache, cephalalgia C0334299 Carcinoid tumor no icd-o subtype HSDN C0085632 Listlessness C2985524 Rhabdoid tumor predisposition syndrome MalaCards C3146279 Coma C1306856 Megaloblastic anemia due to inborn errors of metabolism MalaCards C2237041 Shox gene with short stature C0796101 Digito-orofacial syndrome viii MalaCards C1963064 Anxiety adverse event C0022134 Islet cell adenoma MalaCards C0023012 Delay language C1848488 Pierre robin syndrome with fetal chondrodysplasia OrphaNet|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0699744 Infection of ear HSDN C1384666 Decreased hearing C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant HPO C0332573 Macula C0263637 Angioma serpiginosum, x-linked MalaCards C0036572 Convulsion C0342765 D-glyceric aciduria HPO C1549543 Administration method - pain C0022650 Kidney calculi HSDN C0020673 Hypothermia (central) (local) C1690964 Cataract HSDN C1963077 Bone pain adverse event C0011608 Dermatitis herpetiformis MalaCards C1963093 Dizziness adverse event C0019562 Von hippel-lindau syndrome HSDN C2911645 Weight loss adverse event C0854176 Malignant hepato-biliary neoplasm MalaCards C0018681 Headache, cephalalgia C4048184 Trochlear nerve diseases HSDN C0018681 Headache, cephalalgia C0017638 Glioma HSDN C0039070 Collapse fleeting C0037286 Skin neoplasms HSDN C0030193 Sense of pain C0005417 Bile duct fistula HSDN C0007758 Cerebellar ataxia C4024961 Metachromatic leukodystrophy variant MalaCards C4084769 Vomiting frequency C0018213 Graves disease HSDN C0522224 Palsied C0036983 Septic shock HSDN C2911647 Weight gain adverse event C0032897 Prader-willi syndrome HSDN C0023530 Leukopenia C3280026 Hermansky-pudlak syndrome 9 MalaCards C4085317 Diarrhea frequency C0004030 Aspergillosis HSDN C1549543 Administration method - pain C0034628 Radius fracture HSDN C0042963 Symptoms vomiting C1623041 Breast-fed HSDN C0026838 Spasticity muscle C0023467 Leukemia, myelocytic, acute HSDN C0518090 Frequency of pain question C0017924 Glycogen storage disease type v HSDN C0036572 Convulsion C0795941 Brachycephaly-deafness-cataract-microstomia-mental retardation syndrome MalaCards|UMLS C1963249 Tinnitus adverse event C1720777 Functional laterality HSDN C0520909 Ponv C0043121 Wernicke encephalopathy HSDN C0020305 Fetal edema C3469186 Hemochromatosis, type 1 HSDN C0015938 Fetal macrosomia C2239176 Liver carcinoma HSDN C0027498 Nausea vomiting C2347126 Microscopic polyarteritis MalaCards C0242936 Center pain C0206743 Rhabdoid tumor HSDN C0013421 Dystonia C0812393 Cancer patients and suicide and depression HSDN C0000737 Abdomen pain C0041582 Ulcer HSDN C0026826 High muscle tone C0796101 Digito-orofacial syndrome viii MalaCards C2984058 Have pain C0024419 Waldenstrom macroglobulinemia HSDN C2911647 Weight gain adverse event C0018891 Animal helminthiases HSDN C4084766 Vomiting C0878544 Cardiomyopathies HSDN C0007398 Catatonic C0038454 Cerebrovascular accident HSDN C0030193 Sense of pain C0017919 Glycogen storage disease HSDN C3163620 Hypotension adverse event C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C4084726 Distress cough C0018798 Congenital heart defects HSDN C0027497 Queasy C1963119 Stomach ulcer adverse event HSDN C0013404 Respiratory difficulty C0012644 Animal disease models HSDN C0557874 Global developmental delay C0432217 Wolcott-rallison syndrome HPO C0009421 Comatose C1832903 Migraine, sporadic hemiplegic HPO C0020903 Illusion C0004077 Social assertiveness HSDN C0011570 Monopolar depression C1856493 Gaucher disease, norrbottnian type HPO C0004134 Dyssynergia C1552262 Nurse practitioner - family HSDN C0007166 Cardiac output decreased C4050613 Anxiety scale (basc-2) HSDN C2919142 Short stature adverse event C0022541 Kearns-sayre syndrome MalaCards C0042024 Urine incontinence C0033923 Psychomotor function HSDN C0004093 Asthenia C0018674 Head trauma HSDN C0232462 Appetite decrease C0268579 Propionic acidemia HPO|UMLS C4085210 Usual severity pain C0033906 Psychological theories HSDN C0151786 Weakness muscle C1522133 High cholesterol level HSDN C2585575 Recurrent abdominal pains C1864996 Enteric neuropathy, familial MalaCards C0458002 Acquired dysphasias C0234482 Aphasia, semantic UMLS C0349588 Stature short C2020284 Stickler syndrome, type 1 MalaCards C0040034 Thrombocytopenia C0272199 Familial hemophagocytic lymphocytosis MalaCards C0003962 Ascites C0017689 Glucagonoma MalaCards C0043094 Weight gain C0018790 Cardiac arrest HSDN C3539896 Pelvic pain occurs with urination C0041582 Ulcer HSDN C3887638 Failure to thrive in infant C0268186 Congenital glucose-galactose malabsorption MalaCards|HPO C0478664 Lymphadenopathy regional C0029307 Oroya fever MalaCards C0151889 Reflexes tendon increased C3502054 Dentoleukoencephalopathy MalaCards C4085210 Usual severity pain C0032578 Polyploidy HSDN C0010038 Corneal opacity disorder C1843512 Brain small vessel disease with hemorrhage MalaCards|HPO C0424755 Fever symptoms C1546747 Specimen source codes - polyps HSDN C2024893 Cardiovascular surgery result: fatigue C3489393 Hiatal hernia HSDN C4085210 Usual severity pain C0751967 Multiple sclerosis, relapsing-remitting HSDN C0022346 Yellow skin C3273034 Moderately differentiated hepatocellular carcinoma UMLS C0518090 Frequency of pain question C0015663 Fasting HSDN C3146279 Coma C1963229 Retinal detachment adverse event HSDN C0027066 Myoclonic jerking C0017178 Gastrointestinal diseases HSDN C0497406 Over weight C0398370 Lipedema HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040553 Toxocariasis HSDN C0241210 Speaking delay C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C0033774 Skin pruritus C0051981 Anti-leprosy vaccine HSDN C0349588 Stature short C1832592 Hernandez fragoso syndrome OrphaNet|MalaCards C0035229 Respiratory function impaired C1835555 Larynx, congenital partial atresia of OrphaNet|MalaCards C0030552 Paralysis partial C1865384 Amyotrophy, monomelic OrphaNet|HPO|MalaCards C1069915 Vertigo C1866039 Episodic ataxia, type 5 MalaCards C0011570 Monopolar depression C0795907 Conotruncal anomaly face syndrome MalaCards C1963091 Diarrhea adverse event C0003872 Arthritis, psoriatic HSDN C3539895 Pelvic pain occurs with bowel movement C0042996 Vulvitis unspecified HSDN C0020672 Body temperature decreased C0032914 Pre-eclampsia HSDN C0018784 Deafness sensorineural C0268344 Ehlers-danlos syndrome 6b OrphaNet|HPO|MalaCards C1961131 Cough adverse event C0524909 Hepatitis b, chronic HSDN C0003079 Pupillary inequality C0042165 Anterior uveitis HSDN C4084767 Bothered by vomiting C0006434 Burn injury HSDN C1961131 Cough adverse event C0018798 Congenital heart defects HSDN C0018777 Deafness, conductive C3889474 Bardet-biedl syndrome 16 MalaCards C4084767 Bothered by vomiting C0006384 Bundle-branch block HSDN C0030193 Sense of pain C1511302 Breast carcinoma with choriocarcinomatous features UMLS C2129644 Red streaking going up right leg C4011454 Cataract 42 MalaCards C0042571 Vertigo subjective C3648168 Late effects of nontraumatic subarachnoid hemorrhage vertigo UMLS C0015676 Mental fatigue C0033871 Psychiatric status rating scales HSDN C0020305 Fetal edema C0011849 Diabetes mellitus HSDN C1963086 Confusion adverse event C0004576 Babesiosis MalaCards C0040822 D tremors C2936741 Syndrome xxyy OrphaNet|MalaCards C4042891 Sleep wake disorders C1690964 Cataract HSDN C0015469 Facial paralysis C0022408 Arthropathy HSDN C0424755 Fever symptoms C0014849 Esophageal and gastric varices HSDN C4085548 Usual severity dizziness C0035229 Respiratory insufficiency HSDN C4084767 Bothered by vomiting C0001125 Acidosis, lactic HSDN C4020887 Photodysphoria C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards|HPO C0020580 Decreased sensation C0041296 Tuberculosis HSDN C0474368 Childbirth pain C0042266 Vaginismus HSDN C0018991 Paralysis one side of body C0005695 Bladder neoplasm HSDN C3887638 Failure to thrive in infant C0574083 3-methylglutaconic aciduria type 2 MalaCards|HPO C0270948 Neurogenic muscular atrophy C3553719 Amyotrophic lateral sclerosis 18 MalaCards C2029884 Hearing loss by exam C0036421 Systemic scleroderma HSDN C0518090 Frequency of pain question C0012752 Distance discrimination HSDN C0151786 Weakness muscle C0162670 Mitochondrial myopathies HPO C4042891 Sleep wake disorders C0022116 Ischemia HSDN C0242936 Center pain C0041107 Trisomy HSDN C4084775 Usual severity weight loss C1866552 Paragangliomas 2 (disorder) MalaCards C0011991 Loose stools C0007177 Cardiac tamponade HSDN C0474368 Childbirth pain C0152177 Trigeminal neuropathy HSDN C0033774 Skin pruritus C0026640 Mouth neoplasms HSDN C4084725 Usual severity cough C0009447 Common variable immunodeficiency HSDN C1963091 Diarrhea adverse event C1423541 Vangl2 gene HSDN C0151786 Weakness muscle C0025007 Measles HSDN C0018784 Deafness sensorineural C0393551 Madras-type motor neurone disease OrphaNet|MalaCards C0005745 Blepharoptosis C0021345 Infectious mononucleosis MalaCards C0018991 Paralysis one side of body C3810814 Myocardial infarction ecg assessment HSDN C3463815 Feel fatigue C0008073 Developmental disabilities HSDN C1963091 Diarrhea adverse event C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0042024 Urine incontinence C1546847 Entity name part type - family HSDN C0042420 Vasovagal episode C1449593 Cataleptic freezing reaction HSDN C0030193 Sense of pain C0018965 Hematuria HSDN C3463815 Feel fatigue C0037116 Silicosis HSDN C0003467 Angst C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C3812171 Bradycardia by ecg finding C0242342 Sheehan syndrome MalaCards C1557397 Adverse event associated with pain C0001314 Acute disease HSDN C0018834 Brash C0008350 Cholelithiasis HSDN C2237041 Shox gene with short stature C4014934 Imd36 MalaCards C0917816 Deficiency mental C2931816 Chromosome 2, monosomy 2q24 OrphaNet|HPO|MalaCards C0085642 Asphyxia reticularis C1075202 Paronychia HSDN C1963184 Nystagmus adverse event C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C1963091 Diarrhea adverse event C0038160 Staphylococcal infections HSDN C4085210 Usual severity pain C0238288 Muscular dystrophy, facioscapulohumeral HSDN C0003079 Pupillary inequality C0010034 Corneal diseases HSDN C0039070 Collapse fleeting C0033873 Psychiatry HSDN C0000727 Abdomen acute C0017658 Glomerulonephritis HSDN C0000731 Abdomen distention C0220744 Multiple gastrointestinal atresias (disorder) MalaCards C2315100 Pediatric failure to thrive C0220704 Shprintzen syndrome MalaCards|HPO C2984058 Have pain C0020640 Inherited factor ii deficiency HSDN C4084775 Usual severity weight loss C0022744 Knee injury HSDN C0039070 Collapse fleeting C3539760 Mok wt allele HSDN C4084773 Bothered by weight gain C0033845 Pseudotumor cerebri HSDN C0040264 Ear ringing sound C0042769 Virus diseases HSDN C4084802 Usual severity diarrhea C1963083 Cholecystitis adverse event HSDN C0151786 Weakness muscle C0029882 Otitis media HSDN C4084788 Have dizziness C0085183 Neoplasms, second primary HSDN C0030552 Paralysis partial C0016169 Pathologic fistula HSDN C1963091 Diarrhea adverse event C0872996 Q fever vaccine HSDN C0040485 Wryneck C1533847 Disorder of skeletal muscle UMLS C1963087 Constipation adverse event C0031873 Pica disease HSDN C1549543 Administration method - pain C0001126 Renal tubular acidosis HSDN C0405584 Intolerance; sucrose C2077988 Intolerance of sucrose-isomaltose UMLS C4084776 Weight loss C0149521 Pancreatitis, chronic HSDN C4084768 Usual severity vomiting C0011269 Dementia, vascular HSDN C0010200 Cough symptom C2239253 Aneurysm of sinus of valsalva MalaCards C2919142 Short stature adverse event C0013080 Down syndrome MalaCards|HPO C0149651 Clubbing C0265999 Congenital; clubnail UMLS C4084784 Diarrhea C0020295 Hydronephrosis HSDN C0024031 Back pain lower back C0022408 Arthropathy HSDN C0018784 Deafness sensorineural C1418479 Pex7 gene HSDN C0454644 Delayed language development C0796237 Mental retardation, x-linked 30 HPO C0029163 Hemorrhage mouth C0006118 Brain neoplasms HSDN C0011991 Loose stools C0027121 Myositis HSDN C0030552 Paralysis partial C0220679 Ehlers-danlos syndrome, autosomal dominant, type unspecified OrphaNet C3815497 Cough C3887645 Job syndrome OrphaNet|HPO C0040264 Ear ringing sound C0008066 Child behavior disorders HSDN C0009806 Constipate C0025312 Meningomyelocele HSDN C0011991 Loose stools C0014511 Epithelial cyst HSDN C0015468 Face pain C0040438 Ectopic tooth eruption HSDN C0007758 Cerebellar ataxia C1849096 Infantile onset spinocerebellar ataxia OrphaNet|HPO|MalaCards C0575081 Abnormal gait C0007795 Diffuse cerebral sclerosis of schilder MalaCards C3887873 Hearing loss C0024748 Alpha-mannosidosis HSDN C0043094 Weight gain C0001883 Airway obstruction HSDN C4085211 Pain distress question C0012752 Distance discrimination HSDN C1961131 Cough adverse event C0264353 Bronchomalacia HSDN C2024893 Cardiovascular surgery result: fatigue C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0026838 Spasticity muscle C0314657 Genetic predisposition HSDN C3887638 Failure to thrive in infant C2930917 Chromosome 14, trisomy mosaic OrphaNet|MalaCards C0006370 Bulimia C0033975 Psychotic disorders HSDN C3829611 Nausea frequency C0520679 Sleep apnea, obstructive HSDN C0002962 Angina C0032229 Pleural neoplasms HSDN C3641756 Have diarrhea C1547046 Kind of quantity - taste HSDN C0270948 Neurogenic muscular atrophy C0221060 Mobius syndrome MalaCards|HPO C3665492 Pigmentations C0391816 Tietz syndrome MalaCards C0037771 Paraparesis spastic C0085209 Bovine spongiform encephalitis HSDN C3539023 Pelvic pain increasing in frequency C0007860 Uterine cervicitis HSDN C2048468 Inability to impregnate C0853662 Oestrogen deficiency OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C1961100 Erectile dysfunction adverse event HSDN C1963091 Diarrhea adverse event C0238027 Botulism, infantile MalaCards C0009398 Color vision defects C1832466 Capos syndrome OrphaNet|HPO C0042798 Vision dim C1856689 Friedreich ataxia 1 HPO C0427068 Legs weakness C1858106 Spastic paraplegia 12, autosomal dominant (disorder) MalaCards|HPO C0152459 Striae C0029442 Osteomalacia HSDN C0557874 Global developmental delay C0342783 Deficiency of butyryl-coa dehydrogenase MalaCards|HPO C0018784 Deafness sensorineural C1706377 Memory device component HSDN C0022346 Yellow skin C2930852 Zellweger leukodystrophy MalaCards C0018681 Headache, cephalalgia C0280787 Adult anaplastic ependymoma UMLS C0240735 Personality change C1858991 Childhood ataxia with central nervous system hypomyelinization MalaCards|HPO|UMLS C1557397 Adverse event associated with pain C0006309 Brucellosis HSDN C4085548 Usual severity dizziness C0004153 Atherosclerosis HSDN C1549543 Administration method - pain C0026703 Mucopolysaccharidoses HSDN C0020580 Decreased sensation C1394891 Intrinsic factor deficiency MalaCards|HPO C0009792 Consciousness disorder C0040053 Thrombosis HSDN C2024878 Cardiovascular surgery result: dyspnea C2239176 Liver carcinoma MalaCards|HSDN C4084775 Usual severity weight loss C0019270 Hernia HSDN C4084766 Vomiting C0024841 Matrimony, matrimonial HSDN C0020578 Hyperventilate C0032914 Pre-eclampsia HSDN C4085317 Diarrhea frequency C0520946 Emotional hypersensitivity HSDN C0233514 Behavior abnormal C1849722 Polyglucosan body disease, adult form OrphaNet|HPO|MalaCards C0034150 Skin purpura C0038000 Spleen rupture HSDN C0004134 Dyssynergia C0795910 Cowchock syndrome MalaCards|HPO C0022408 Disorder joint C1837657 Spondyloepiphyseal dysplasia, omani type MalaCards C1963184 Nystagmus adverse event C1836669 Congenital disorder of glycosylation, type if MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C1962986 Glaucoma adverse event HSDN C0030200 Intractable pain C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3665492 Pigmentations C0027656 Neoplasms, connective tissue MalaCards C0018772 Deafness C1866094 Deafness, autosomal recessive 15 MalaCards|HPO C4085549 Dizziness C0034065 Pulmonary embolism HSDN C1549543 Administration method - pain C0242231 Coronary stenosis HSDN C4085222 Nausea C0013182 Drug allergy HSDN C0349588 Stature short C1836861 Fanconi anemia, complementation group i MalaCards|HPO C0037317 Sleep disturbance C3493776 Hypothyroidism, congenital, nongoitrous, 1 MalaCards C0042571 Vertigo subjective C4084909 Depression subordinate domain HSDN C0018681 Headache, cephalalgia C0600260 Lung diseases, obstructive HSDN C0040460 Dental pain C0011849 Diabetes mellitus HSDN C0042798 Vision dim C1969562 Mental retardation, autosomal dominant 1 HPO C0003962 Ascites C0085404 Poems syndrome MalaCards C3815497 Cough C0036329 Schistosomiasis japonica DiseaseOntology C4084775 Usual severity weight loss C0679360 Foodborne disease HSDN C0030486 Extremity paralysis, lower C3714605 Of pain perception HSDN C1557397 Adverse event associated with pain C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C1961131 Cough adverse event C0014851 Cyst, esophageal HSDN C0007758 Cerebellar ataxia C1970808 Xeroderma pigmentosum b-cockayne syndrome HPO C0750394 Wbc low C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C0027796 Neuralgias C2004491 Cicatrix HSDN C0018681 Headache, cephalalgia C0013336 Dwarfism HSDN C0518090 Frequency of pain question C0162869 Aneurysm, ruptured HSDN C0085636 Light sensitivity C3495589 Jalili syndrome OrphaNet|UMLS|HPO|MalaCards C4085222 Nausea C0042164 Uveitis HSDN C0042940 Disorder of voice C0014541 Epiglottitis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0020550 Hyperthyroidism HSDN C4084767 Bothered by vomiting C2062326 Eosinophilic enteropathy OrphaNet|MalaCards C0023012 Delay language C2931840 Aspartylglucosamidase (aga) deficiency OrphaNet|HPO|MalaCards C3898969 Have been vomiting C1622510 Neurocytoma HSDN C0018834 Brash C2752089 Neuropathy, hereditary sensory and autonomic, type iia HPO C0010200 Cough symptom C1334666 Mediastinal malignant non-seminomatous germ cell neoplasm UMLS C0497406 Over weight C0028768 Obsessive-compulsive disorder HSDN C4048158 Convulsions C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C1961131 Cough adverse event C0018916 Hemangioma HSDN C0013404 Respiratory difficulty C0024421 Macroglossia HSDN C0036572 Convulsion C1861785 Cavernous malformations of cns and retina HPO C0013404 Respiratory difficulty C0023903 Liver neoplasms MalaCards|HSDN C1963087 Constipation adverse event C4049644 Depression HSDN C1000483 Genus anemia C2931371 Umbilical cord ulcer with intestinal atresia MalaCards C0038002 Spleen enlargement C0039373 Tay-sachs disease OrphaNet|MalaCards C0037316 Not enough sleeping C0010598 Cyclothymic disorder HSDN C0751295 Memory loss or impairment C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C0010200 Cough symptom C0024299 Lymphoma HSDN|UMLS C4084775 Usual severity weight loss C1963233 Seroma adverse event HSDN C3641755 Have constipation C1334818 Multicystic mesothelioma of peritoneum MalaCards C1963281 Vomiting adverse event C4084909 Depression subordinate domain HSDN C4085548 Usual severity dizziness C1546533 Specimen source codes - abscess HSDN C0424755 Fever symptoms C0022810 Disease, kyasanur forest MalaCards C0233514 Behavior abnormal C0751278 Metachromatic leukodystrophy, infant MalaCards C0009421 Comatose C0025517 Metabolic diseases HSDN C1962972 Proteinuria adverse event C0017638 Glioma HSDN C0027498 Nausea vomiting C0032339 Rothmund-thomson syndrome MalaCards C0237326 Defecation pain C0796095 Opitz trigonocephaly syndrome MalaCards|HPO C4085549 Dizziness C0002989 Epithelioid hemangioma of skin HSDN C4050613 Anxiety C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0162298 Stiffness joints C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0034933 Abnormal reflexes C0037952 Spinocerebellar degeneration HSDN C1000483 Genus anemia C1837174 Hemophagocytic lymphohistiocytosis, familial, 3 MalaCards|HPO C0030193 Sense of pain C0221074 Depression, postpartum HSDN C4084784 Diarrhea C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C1705812 Nci thesaurus role HSDN C4085210 Usual severity pain C0004589 B. anthracis HSDN C2024878 Cardiovascular surgery result: dyspnea C0460137 Push down or depress HSDN C2237041 Shox gene with short stature C3151120 Meier-gorlin syndrome 4 MalaCards C2237041 Shox gene with short stature C3806742 Colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation MalaCards C0332573 Macula C0855018 Stage iv acral lentiginous melanoma UMLS C2984058 Have pain C0030470 Paranasal sinus neoplasms HSDN C0278125 Crossed extensor reflex C0278122 Consensual reflex UMLS C0234132 Pyramidal sign C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards|HPO C0522224 Palsied C0009651 Conditioning operant HSDN C2187990 Unable to perform sex C0025286 Meningioma MalaCards C0018991 Paralysis one side of body C0027663 Neoplasms, multiple primary HSDN C0036396 Sciatica C0206734 Hemangioblastoma HSDN C3203358 Alveolar hypoventilation C0039978 Thoracic diseases HSDN C1963170 Hypothermia adverse event C0010674 Cystic fibrosis HSDN C0007398 Catatonic C0014549 Tonic-clonic epilepsy HSDN C0013604 Edematous C0016978 Gallbladder neoplasm HSDN C0026826 High muscle tone C0751285 Maple syrup urine disease, thiamine responsive HPO C0013421 Dystonia C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards C0026826 High muscle tone C1848211 Mental retardation with psychosis, pyramidal signs, and macroorchidism MalaCards C1963091 Diarrhea adverse event C0032002 Pituitary diseases HSDN C3815497 Cough C0742343 Acute chest syndrome DiseaseOntology|HSDN|MalaCards C0007398 Catatonic C0033906 Psychological theories HSDN C0042571 Vertigo subjective C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C3815497 Cough C0032231 Pleurisy HSDN C0002965 Crescendo angina C0003490 Aortic arch syndrome HSDN C0030200 Intractable pain C2239176 Liver carcinoma HSDN C0042928 Paralysis vocal cord C0029896 Disease, ent HSDN C1260880 Nasal drip C0280333 Nasal cavity squamous cell carcinoma UMLS C1069915 Vertigo C0013808 Electroconvulsive therapy HSDN C0010200 Cough symptom C0037928 Spinal cord diseases HSDN C3494358 Characteristic, prodromal C4085311 Depression - recess HSDN C0005745 Blepharoptosis C3280231 Chromosome 8q21.11 deletion syndrome MalaCards C0036572 Convulsion C3809522 Infantile liver failure syndrome 1 MalaCards|UMLS C0030552 Paralysis partial C2931928 Mitochondrial cytopathy MalaCards C2029884 Hearing loss by exam C0453996 Tobacco smoking HSDN C0011991 Loose stools C0024620 Primary malignant neoplasm of liver MalaCards C1145670 Failure respiratory C1859407 Bone dysplasia, lethal, holmgren type OrphaNet|MalaCards C0028738 Nystagmus C0339535 Night blindness, congenital stationary MalaCards|HPO C0013595 Eczematous dermatitis C2931746 Sulfocysteinuria HPO C0751495 Seizure focal C0042029 Urinary tract infection UMLS C0036572 Convulsion C0010709 Cyst HSDN C0398650 Idiopathic thrombocytopenia purpura C0836924 Thrombocytosis HSDN C0004134 Dyssynergia C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards C0700590 Diaphoresis excessive C0263628 Tumoral calcinosis MalaCards C3541349 Syncope C0040028 Thrombocythemia, essential MalaCards C1961131 Cough adverse event C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards C0011991 Loose stools C0028796 Dermatitis, occupational HSDN C4084768 Usual severity vomiting C0027819 Neuroblastoma HSDN C0022346 Yellow skin C0021831 Intestinal diseases HSDN C0009398 Color vision defects C0010068 Coronary heart disease HSDN C2984058 Have pain C2936490 Cardiac arrest, out-of-hospital HSDN C4084788 Have dizziness C0007781 Intracranial embolism and thrombosis HSDN C4085549 Dizziness C0001883 Airway obstruction HSDN C0032227 Effusion pleural C2931242 Familial waldmann's disease MalaCards C0085606 Urination urgency C1849140 Spastic ataxia, charlevoix-saguenay type MalaCards|HPO C4085210 Usual severity pain C0043019 Lateral medullary syndrome HSDN C3163620 Hypotension adverse event C3164344 Adult onset autosomal dominant leukodystrophy OrphaNet|HPO C0027066 Myoclonic jerking C0022661 Kidney failure, chronic UMLS C0016382 Cutaneous vascular engorgement C0263313 Pemphigus foliaceus OrphaNet|MalaCards C3641755 Have constipation C0001122 Acidosis HSDN C2024893 Cardiovascular surgery result: fatigue C0700208 Acquired scoliosis HSDN C2237041 Shox gene with short stature C1578691 Congenital myxedema MalaCards C0027498 Nausea vomiting C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C0019209 Large liver C0030328 Panniculitis, nodular nonsuppurative MalaCards C0518090 Frequency of pain question C0007760 Cerebellar diseases HSDN C1961131 Cough adverse event C0004238 Atrial fibrillation HSDN C1279888 Proteinuria of undiagnosed cause C0003496 Aortic rupture HSDN C0231218 Malaise generalized C0861876 Recurrent hepatocellular carcinoma UMLS C0008031 Pain chest C0314657 Genetic predisposition HSDN C0242670 Chronic vegetative state C0001889 Akinetic mutism HSDN C2029884 Hearing loss by exam C0033871 Psychiatric status rating scales HSDN C0277959 Hair coarseness C0406355 Acrokeratosis paraneoplastica of bazex MalaCards C4085862 Bothered by nausea C3839212 Familial hyperaldosteronism type 2 MalaCards C2911647 Weight gain adverse event C0042510 Ventricular fibrillation HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038012 Spondylitis HSDN C1963281 Vomiting adverse event C0020540 Malignant hypertension HSDN C0206160 Retic count elevated C0221018 Hereditary sideroblastic anemia HSDN C0015300 Ocular proptosis C1864825 Frias syndrome MalaCards C0039070 Collapse fleeting C0027902 Neuropsychological diagnosis HSDN C0007642 Cellulitis nos C1853490 22q13.3 deletion syndrome MalaCards|HPO C0576456 Poor feeding C4015186 Monocarboxylate transporter 1 deficiency MalaCards C0026826 High muscle tone C1849700 Hyperphenylalaninemia with primapterinuria MalaCards|HPO C4084723 Constipation C0022660 Kidney failure, acute HSDN C1838869 Proximal neurogenic muscle weakness C0546264 Congenital fiber type disproportion HPO C0026838 Spasticity muscle C1836522 Schindler disease, type ii MalaCards C4085211 Pain distress question C0161410 Accessory nerve injuries HSDN C4084727 Cough frequency C0023448 Lymphoid leukemia HSDN C4085642 Level of joint stiffness C1847593 Epiphyseal dysplasia, multiple, 4 MalaCards C0497406 Over weight C0242383 Age related macular degeneration HSDN C2129379 Right elbow is 'frozen' C0016059 Fibrosis UMLS C0333243 Edema pitting C0018802 Congestive heart failure UMLS C0026821 Cramp C0002170 Alopecia HSDN C0024031 Back pain lower back C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C1963071 Back pain adverse event C0006309 Brucellosis DiseaseOntology|MalaCards C0004134 Dyssynergia C0271829 Pendred's syndrome MalaCards|HPO C3898969 Have been vomiting C0040156 Thyrotoxicosis HSDN C4085548 Usual severity dizziness C0006145 Breast diseases HSDN C2032395 Pelvic pain on the left C0563150 Catastrophization HSDN C0522224 Palsied C0040361 Togaviridae infections HSDN C1959630 Eye pain adverse event C1319688 Blister dose form HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0022568 Keratitis HSDN C3887873 Hearing loss C0033923 Psychomotor function HSDN C0015468 Face pain C2025995 Cellulitis HSDN C0242936 Center pain C0027626 Neoplasm invasiveness HSDN C0018681 Headache, cephalalgia C0524620 Metabolic syndrome x HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020179 Huntington disease HSDN C0085631 Abnormal excitement C0033936 Psychoses, alcoholic HSDN C0007642 Cellulitis nos C0015773 Felty syndrome MalaCards C0232466 Feeding difficulty C4015357 Mental retardation, autosomal dominant 31 MalaCards C2315100 Pediatric failure to thrive C0342731 Deficiency of mevalonate kinase MalaCards C0040822 D tremors C1849700 Hyperphenylalaninemia with primapterinuria MalaCards|HPO C0022346 Yellow skin C0270215 Breast milk jaundice UMLS C0003467 Angst C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0024031 Back pain lower back C0006142 Malignant neoplasm of breast UMLS C0557874 Global developmental delay C1835820 Holoprosencephaly 7 HPO C0030554 Abnormal sensation C0027830 Neurofibroma HSDN C0454644 Delayed language development C4015167 Mental retardation, autosomal dominant 30 MalaCards C0035229 Respiratory function impaired C0265245 Nager syndrome OrphaNet|HPO|MalaCards C2984058 Have pain C0007772 Intracranial arteriovenous malformation HSDN C0039870 Leanness C1000483 Genus anemia HSDN C3665347 Vision impaired C1852267 Optic atrophy 1 and deafness HPO C0018681 Headache, cephalalgia C0011630 Dermatomycoses HSDN C2024893 Cardiovascular surgery result: fatigue C0001546 Adjustment disorders HSDN C0020615 Hypoglycemia nos C0079541 Holoprosencephaly OrphaNet|MalaCards C0476273 Distress respiratory C1334682 Mediastinal teratoma UMLS C0018772 Deafness C0017412 Genital diseases, male HSDN C1963249 Tinnitus adverse event C0004936 Mental disorders HSDN C2032332 Bilateral tmj pain C0039496 Temporomandibular joint dysfunction syndrome UMLS C0037317 Sleep disturbance C0587248 Costello syndrome (disorder) MalaCards C0003811 Cardiac rhythm disturbance C0268579 Propionic acidemia OrphaNet|HPO C0037316 Not enough sleeping C3146297 Study of behavior during childhood HSDN C0009806 Constipate C0003507 Aortic valve stenosis HSDN C0032914 Toxemia C0020217 Hydatidiform mole OrphaNet|MalaCards C0565619 Distress fetal labor C0015930 Fetal distress UMLS C4084775 Usual severity weight loss C0038395 Streptococcal infections HSDN C0039070 Collapse fleeting C0162316 Iron deficiency anemia UMLS C0424755 Fever symptoms C0002694 Amputation traumatic HSDN C3815497 Cough C1866983 Scleroderma, familial progressive MalaCards C4084725 Usual severity cough C3887645 Job syndrome OrphaNet|HPO C0263629 Tumor-like lesions of the skin C0263640 Angiokeratoma of mibelli UMLS C0018991 Paralysis one side of body C0020517 Hypersensitivity HSDN C0016382 Cutaneous vascular engorgement C0030271 Pancoast syndrome HSDN C2919142 Short stature adverse event C0795914 Crome syndrome OrphaNet|MalaCards C3714552 Strength decreased C3250443 Myotonic dystrophy 1 MalaCards|UMLS C4085211 Pain distress question C0162832 Apc HSDN C0242936 Center pain C0019348 Herpes simplex infections HSDN C0023015 Language handicap C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C0270948 Neurogenic muscular atrophy C4015461 Ruijs-aalfs syndrome MalaCards C1279511 Malarial pigment deposition C3665492 Structure showing abnormal deposition of pigment (morphologic abnormality) UMLS C4084768 Usual severity vomiting C0338480 Common migraine HSDN C3274924 Have been coughing C0038354 Stomach diseases HSDN C0015672 Decreased energy C0037304 Skull fracture HSDN C4084769 Vomiting frequency C0037199 Sinusitis HSDN C0043094 Weight gain C0034494 Rabies (disorder) HSDN C1963180 Neck pain adverse event C0023055 Laryngeal neoplasm HSDN C0000737 Abdomen pain C1332262 Anal canal squamous cell carcinoma MalaCards C2108109 Continuous electrocardiogram sinus tachycardia C1866552 Paragangliomas 2 (disorder) MalaCards C3641756 Have diarrhea C1145670 Respiratory failure HSDN C0231791 In toe C1842870 Chromosome 1p36 deletion syndrome MalaCards C0003862 Pain joint C0085253 Adult-onset still disease OrphaNet|MalaCards C3641755 Have constipation C3244301 Coverage level - family HSDN C3463815 Feel fatigue C0023487 Acute promyelocytic leukemia HSDN C0000737 Abdomen pain C0020540 Malignant hypertension UMLS C0000737 Abdomen pain C0033968 Psychotherapeutic technique HSDN C0015230 Exanthem C0343052 Guttate psoriasis UMLS C0030232 Color loss C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|HPO|MalaCards C2203646 Jaundice C3244301 Coverage level - family HSDN C0030193 Sense of pain C0027531 Neck injury HSDN C0030193 Sense of pain C0022366 Jaw, edentulous HSDN C4085642 Level of joint stiffness C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0006277 Bronchitis C1876175 Ataxia-telangiectasia variant MalaCards C0728710 Pupil constriction observed C4014557 Myopathy, tubular aggregate, 2 MalaCards C2911645 Weight loss adverse event C1134719 Invasive ductal breast carcinoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018567 Hand dermatoses HSDN C2984058 Have pain C0206647 Dermatofibrosarcoma HSDN C1549543 Administration method - pain C0023860 Listeriosis HSDN C4084725 Usual severity cough C0012979 Canine disease HSDN C0917816 Deficiency mental C1282843 Lysine intolerance HPO C2984058 Have pain C0002312 Alpha-thalassemia HSDN C4084726 Distress cough C0525045 Mood disorders HSDN C4084725 Usual severity cough C0236969 Substance-related disorders HSDN C2984058 Have pain C0024692 Mandible fracture HSDN C1963063 Anorexia adverse event C0334663 Histiocytic sarcoma HSDN C3829611 Nausea frequency C0020545 Hypertension, renovascular HSDN C0015938 Fetal macrosomia C1415001 Gbe1 gene HSDN C0000727 Abdomen acute C0460137 Push down or depress HSDN C0413252 Hypothermia due to exposure C0751865 Alcohol-induced disorders, nervous system HSDN C0021359 Infertility C0860159 Partial androgen resistance OrphaNet|HPO C0042798 Vision dim C1261128 Progeria-like syndrome MalaCards C0004604 Pain back C0812393 Cancer patients and suicide and depression HSDN C0034150 Skin purpura C1962983 Cataract adverse event HSDN C0231528 Muscle pain generalized C0036391 Schwartz-jampel syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C2931660 Autosomal recessive fructose 1, 6-diphosphatase deficiency MalaCards C4084788 Have dizziness C0000833 Abscess HSDN C3665347 Vision impaired C1832174 Doyne honeycomb retinal dystrophy HPO C0007758 Cerebellar ataxia C0003811 Cardiac arrhythmia HSDN C3539889 Pelvic pain increasing in severity C0206622 Adenomyoma HSDN C0557874 Global developmental delay C1846331 Juvenile-onset dystonia MalaCards C0039070 Collapse fleeting C0013010 Cerebral lateralization HSDN C0557874 Global developmental delay C3553816 Spinocerebellar ataxia, autosomal recessive 13 MalaCards C0542476 Forgetful C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0011981 Diaphragmatic eventration HSDN C0015469 Facial paralysis C0025183 Meige syndrome HSDN C0013421 Dystonia C0040136 Thyroid neoplasm HSDN C0332573 Macula C0855016 Stage ii acral lentiginous melanoma UMLS C0007398 Catatonic C0025309 Meningoencephalitis HSDN C3898969 Have been vomiting C0015927 Intrauterine fetal demise HSDN C1963093 Dizziness adverse event C0009241 Cognition disorders HSDN C4085211 Pain distress question C0026771 Trauma multiple HSDN C3898969 Have been vomiting C0004052 Aspiration of vomitus HSDN C4085862 Bothered by nausea C0035435 Rheumatism HSDN C0030232 Color loss C0022638 Ketosis HSDN C3829611 Nausea frequency C1258215 Ileus HSDN C4084784 Diarrhea C0006663 Calcinosis HSDN C0018772 Deafness C2963140 Arteriovenous fistula in use with two needles HSDN C0344374 Fecal overflow C0015732 Fecal incontinence UMLS C4084774 Have weight loss C1548578 Location characteristic id - smoking HSDN C0000737 Abdomen pain C0024221 Lymphangioma HSDN C4085211 Pain distress question C0152177 Trigeminal neuropathy HSDN C0015469 Facial paralysis C0035066 Renal artery obstruction HSDN C2029884 Hearing loss by exam C0017921 Glycogen storage disease type ii MalaCards C0020672 Body temperature decreased C0031511 Pheochromocytoma HSDN C4085211 Pain distress question C0007894 Cestode infections HSDN C0007758 Cerebellar ataxia C1832903 Migraine, sporadic hemiplegic HPO C0848203 Male pelvic pain C0206622 Adenomyoma HSDN C0043352 Absent salivary secretion C0206138 Crest syndrome MalaCards C0010200 Cough symptom C0037579 Soft tissue neoplasms HSDN C0349588 Stature short C2752074 Alpha-ketoglutarate dehydrogenase deficiency OrphaNet|HPO|MalaCards C2029884 Hearing loss by exam C3539923 Cdisc adas-cog - orientation summary score HSDN C0037763 Spasm C1522133 High cholesterol level HSDN C0015672 Decreased energy C2931242 Familial waldmann's disease MalaCards C0030200 Intractable pain C0162871 Aortic aneurysm, abdominal HSDN C1838869 Proximal neurogenic muscle weakness C1970211 Spinal muscular atrophy, distal, autosomal recessive, 4 MalaCards|HPO C0851578 Disorder sleep C2609414 Acute kidney injury HSDN C2984057 Have nausea C1866552 Paragangliomas 2 (disorder) MalaCards C3815497 Cough C0007787 Transient ischemic attack HSDN C0036659 Sensation disorder C1412124 Acls gene HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C2751898 Ventricular fibrillation, paroxysmal familial, 1 HPO C0040485 Wryneck C0038661 Suicide HSDN C0751460 Flaccid quadriplegia C0034372 Quadriplegia UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0751774 Nocturnal myoclonus syndrome HSDN C0018681 Headache, cephalalgia C0017416 Genital neoplasms, female HSDN C0020578 Hyperventilate C1881674 Medical device emits smoke HSDN C0162835 Hypopigmentation C2930923 N-acetylneuraminic acid storage disease HPO C0042963 Symptoms vomiting C0085693 Acute appendicitis nos (disorder) MalaCards C0231218 Malaise generalized C3273034 Moderately differentiated hepatocellular carcinoma UMLS C1557397 Adverse event associated with pain C1705811 Terminology role entity HSDN C0020673 Hypothermia (central) (local) C0036690 Septicemia HSDN C4084769 Vomiting frequency C0017160 Gastroenteritis DiseaseOntology C0007815 Cerebrospinal fluid rhinorrhoea C0016542 Foreign body HSDN C0398650 Idiopathic thrombocytopenia purpura C0021368 Inflammation HSDN C1279888 Proteinuria of undiagnosed cause C3489393 Hiatal hernia HSDN C0004134 Dyssynergia C1145670 Respiratory failure HSDN C0221752 Rbc urine C0268646 Isolated cystinuria OrphaNet|MalaCards C0011991 Loose stools C0870082 Hyperkeratosis HSDN C1579931 Depressed - symptom C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C2937287 Hematolysis HSDN C4085222 Nausea C0554114 Epstein-barr virus hepatitis MalaCards C4084775 Usual severity weight loss C2347126 Microscopic polyarteritis HSDN C0030554 Abnormal sensation C0037286 Skin neoplasms HSDN C1971624 Appetite absent C0860549 Refeed syndrome HSDN C3665386 Abnormal vision C0268680 Biotin deficiency MalaCards C0413252 Hypothermia due to exposure C0040128 Thyroid diseases HSDN C0011991 Loose stools C0031873 Pica disease HSDN C0234146 Absent reflex C2675527 Myopathy, congenital, compton-north MalaCards|HPO C4085317 Diarrhea frequency C0023223 Leg ulcer HSDN C0043094 Weight gain C0000771 Abnormalities, drug induced HSDN C0848203 Male pelvic pain C0042373 Vascular diseases HSDN C1557397 Adverse event associated with pain C0029944 Drug overdose HSDN C0036659 Sensation disorder C0752287 Sleep disorders, intrinsic HSDN C2881389 Other subjective visual disturbances C0809996 Blindness and vision defects UMLS C4084773 Bothered by weight gain C0002453 Amenorrhea HSDN C2315100 Pediatric failure to thrive C1848578 Methylmalonic aciduria and homocystinuria, cblf type (disorder) OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0038436 Post-traumatic stress disorder HSDN C0497406 Over weight C0001624 Adrenal gland neoplasms HSDN C0004134 Dyssynergia C3244301 Coverage level - family HSDN C0221232 Welts C0263347 Urticaria medicamentosa UMLS C0917816 Deficiency mental C2751651 Chromosome 19q13.11 deletion syndrome OrphaNet|MalaCards C0413252 Hypothermia due to exposure C0242488 Acute lung injury HSDN C4085549 Dizziness C0018081 Gonorrhea HSDN C2237041 Shox gene with short stature C0271972 Thiamine-responsive megaloblastic anemia MalaCards C2919142 Short stature adverse event C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C4084727 Cough frequency C0206138 Crest syndrome MalaCards C1557397 Adverse event associated with pain C0032372 Poliomyelitis, anterior, acute HSDN C0018991 Paralysis one side of body C0014059 Encephalomyelitis, acute disseminated HSDN C1963184 Nystagmus adverse event C1832466 Capos syndrome HPO C0034151 Hyperglobulinemic purpura C0016398 Focal infection, dental HSDN C2875625 Eyelid retraction right lower eyelid C0497217 Other disease of eye UMLS C4084769 Vomiting frequency C0026780 Mumps HSDN C0032617 High urine output C1847013 Nephronophthisis 4 MalaCards|HPO|UMLS C0000737 Abdomen pain C0242184 Hypoxia UMLS C4085661 Usual severity nausea C0948039 Bacterial gastritis MalaCards C0004134 Dyssynergia C0027927 Neurosyphilis HSDN C0242936 Center pain C0037889 Hereditary spherocytosis HSDN C4084766 Vomiting C1847839 Episodic ataxia, type 3 MalaCards C1557397 Adverse event associated with pain C0037221 Situs inversus HSDN C2984058 Have pain C0270857 Epilepsy, reflex HSDN C0042963 Symptoms vomiting C0401160 Chemotherapy induced nausea vomiting UMLS C0271215 Blindness legal C1956390 Cranial arteritis MalaCards C1962957 Flushing adverse event C0149931 Migraine disorders HSDN C1557397 Adverse event associated with pain C0006818 Campylobacter infection HSDN C0020438 Hypercalciuria C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C2240374 Eosinophil count raised HSDN C0242936 Center pain C0014394 Enuresis HSDN C2029884 Hearing loss by exam C0265354 Charge syndrome HSDN C0013604 Edematous C0235833 Congenital diaphragmatic hernia HSDN C1549543 Administration method - pain C0178282 Hernia of abdominal cavity HSDN C4084802 Usual severity diarrhea C0018674 Head trauma HSDN C0851578 Disorder sleep C0517960 Neurological status: consciousness HSDN C0004310 Auditory disorder process C0026613 Motor skills disorders HSDN C2911647 Weight gain adverse event C0030472 Paraneoplastic syndromes HSDN C2032395 Pelvic pain on the left C0206622 Adenomyoma HSDN C0002962 Angina C1258104 Diffuse scleroderma HSDN C0042571 Vertigo subjective C1834559 Continuous muscle fiber activity, hereditary HPO C1000483 Genus anemia C0014084 Enchondromatosis MalaCards|HPO C0004134 Dyssynergia C0268425 Alstrom syndrome HSDN C0004134 Dyssynergia C0004114 Astrocytoma HSDN C3539020 Pelvic pain decreasing in frequency C0010709 Cyst HSDN C0413252 Hypothermia due to exposure C0042514 Tachycardia, ventricular HSDN C1384666 Decreased hearing C1834928 Cloverleaf skull micromelia thoracic dysplasia OrphaNet|HPO|MalaCards C0022346 Yellow skin C0272126 Evans syndrome OrphaNet|MalaCards C4084723 Constipation C0079541 Holoprosencephaly MalaCards C0234378 Postural tremor C0917796 Optic atrophy, hereditary, leber HPO|UMLS C3887873 Hearing loss C0270972 Cornelia de lange syndrome HSDN C0009806 Constipate C3554520 Ufs2 MalaCards|UMLS C4084766 Vomiting C0004933 Behavior modification technique HSDN C2984057 Have nausea C0497327 Dementia HSDN C2024878 Cardiovascular surgery result: dyspnea C0009375 Colonic neoplasms HSDN C3163620 Hypotension adverse event C2678367 Renal tubular dysgenesis with choanal atresia and athelia HPO C4084768 Usual severity vomiting C0023521 Globoid cell leukodystrophy MalaCards|HPO C0013608 Cardiac edema C0043049 Water intoxication HSDN C0009806 Constipate C1839332 Rett syndrome, preserved speech variant HPO C1961131 Cough adverse event C0004153 Atherosclerosis HSDN C1279888 Proteinuria of undiagnosed cause C0019829 Hodgkin disease HSDN C0013604 Edematous C0003860 Arteritis HSDN C0004604 Pain back C0014547 Epilepsies, partial HSDN C0747556 Pharyngitis recurrent C0023241 Legionnaires' disease MalaCards C1000483 Genus anemia C1855869 Autoimmune polyendocrinopathy syndrome, type i, autosomal dominant HPO C0040822 D tremors C0013182 Drug allergy HSDN C3815497 Cough C0014836 Escherichia coli infections HSDN C2911645 Weight loss adverse event C0013336 Dwarfism HSDN C0851578 Disorder sleep C0017185 Gastrointestinal neoplasms HSDN C0013428 Painful urination C3150878 Hyperoxaluria, primary, type iii MalaCards C0917801 Sleep disorder insomnia C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C1963281 Vomiting adverse event C0006736 Body stone HSDN C1963252 Tremor adverse event C0019202 Hepatolenticular degeneration MalaCards|HPO C0030193 Sense of pain C0042140 Uterine prolapse HSDN C0042025 Urinary incontinence stress C0007097 Carcinomas HSDN C0025323 Bleeding menstrual heavy C1264040 Von willebrand disease, type 2 HPO C4084802 Usual severity diarrhea C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0013428 Painful urination C0855187 Stage 0 bladder squamous cell carcinoma UMLS C3665347 Vision impaired C1859316 Cataract-alopecia-sclerodactyly syndrome OrphaNet|MalaCards C0012569 Double vision C1956391 Temporal arteritis MalaCards|HPO C0042571 Vertigo subjective C0751291 Desmoplastic medulloblastoma MalaCards C0086437 Joint hypermobility C2930971 Acroosteolysis dominant type MalaCards C1000483 Genus anemia C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0151740 Intracranial hypertension C0220658 Pfeiffer syndrome MalaCards C0013404 Respiratory difficulty C0001618 Tumors of adrenal cortex HSDN C2029884 Hearing loss by exam C0017638 Glioma HSDN C0020455 Hypergammaglobulinemia C0302148 Blood clot HSDN C2237041 Shox gene with short stature C1863881 Radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation OrphaNet|MalaCards C3898969 Have been vomiting C0026896 Myasthenia gravis HSDN C0034150 Skin purpura C0268381 Primary amyloidosis MalaCards C4084897 Sleep disturbance subordinate domain C2676739 Chromosome 2q32-q33 deletion syndrome MalaCards|HPO C0033774 Skin pruritus C0026948 Mycosis fungoides MalaCards C0152459 Striae C1306214 Acth-secreting pituitary adenoma HPO C4084775 Usual severity weight loss C0023904 Liver neoplasms, experimental HSDN C0349588 Stature short C0268425 Alstrom syndrome OrphaNet|HPO|MalaCards C3665347 Vision impaired C0035613 Rift valley fever MalaCards C0040485 Wryneck C0152438 Sprengel deformity OrphaNet|MalaCards C1963091 Diarrhea adverse event C1836704 Arrhythmogenic right ventricular dysplasia, familial, 7 MalaCards C0231218 Malaise generalized C3899978 Bclc stage c adult hepatocellular carcinoma UMLS C4085661 Usual severity nausea C1962986 Glaucoma adverse event HSDN C1290643 Extrinsic staining of teeth associated with inadequate oral hygiene C0553565 Posteruptive teeth stain. nos UMLS C0004134 Dyssynergia C2930815 Acute cerebral gaucher disease MalaCards C0018775 Hearing loss bilateral C0020757 Ichthyoses HSDN C4084725 Usual severity cough C1956391 Temporal arteritis MalaCards|HPO C0917816 Deficiency mental C2931070 Schofer beetz bohl syndrome OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0033348 Language program HSDN C3539022 Pelvic pain decreasing in severity C0001442 Adenosarcoma HSDN C0011206 Delirium acute C0700327 Clinical findings relating to memory HSDN C0023015 Language handicap C0010709 Cyst HSDN C4084775 Usual severity weight loss C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0162298 Stiffness joints C2931548 Krasnow qazi yermakov syndrome OrphaNet|MalaCards C0013604 Edematous C0751552 Malignant neoplasm of thymus MalaCards C1963137 Hydrocephalus adverse event C0020305 Hydrops fetalis MalaCards C1963137 Hydrocephalus adverse event C1834928 Cloverleaf skull micromelia thoracic dysplasia MalaCards|HPO C1557397 Adverse event associated with pain C0020445 Hypercholesterolemia, familial HSDN C1963071 Back pain adverse event C3178970 Entrapment, pudendal nerve MalaCards C0002622 Amnesias C1963064 Anxiety adverse event HSDN C0012833 Dizzy C0344435 Ventricular fibrillation by ecg finding HSDN C0007758 Cerebellar ataxia C0007222 Cardiovascular diseases HSDN C4085210 Usual severity pain C0024720 Anxiety scale, manifest HSDN C1557397 Adverse event associated with pain C0854906 Benign schwannoma MalaCards C0458087 Pain at anatomical site C1275009 Painful operation scar UMLS C0002170 Alopecia disorders C0795895 Acd-mental retardation syndrome OrphaNet|MalaCards C3463815 Feel fatigue C0162557 Liver failure, acute HSDN C0015672 Decreased energy C0003851 Arteriosclerosis obliterans HSDN C0041105 Jaw spasm C0453996 Tobacco smoking HSDN C2096293 Ent surgical result ear vertigo C0003490 Aortic arch syndrome HSDN C0151603 Edema generalized C0175692 Johanson-blizzard syndrome MalaCards|HPO C4084784 Diarrhea C0013100 Dracontiasis OrphaNet|MalaCards C2700617 Irritation - emotion C1563705 Nephrogenic diabetes insipidus, type i HPO C1263846 Attention deficit disorder with hyperactivity C0032897 Prader-willi syndrome MalaCards|HPO C0022107 Fussiness C0001622 Adrenal gland hyperfunction OrphaNet C0008031 Pain chest C0031090 Periodontal diseases HSDN C0917816 Deficiency mental C4014745 Mental retardation, autosomal recessive 44 MalaCards C0574002 Foot swelling C0022660 Kidney failure, acute UMLS C0042963 Symptoms vomiting C0027625 Circulating neoplastic cells HSDN C1963281 Vomiting adverse event C0011875 Diabetic angiopathies HSDN C0150055 Pain chronic C4060690 Tumor infiltration UMLS C0019825 Voice hoarseness C0005967 Bone neoplasms HSDN C2096293 Ent surgical result ear vertigo C0752140 Intracranial embolism HSDN C0454644 Delayed language development C1332140 Acrofacial dysostosis MalaCards C0022346 Yellow skin C1096401 Jaundice (excl neonatal) UMLS C0005874 Blush C3887525 Keratosis follicularis spinulosa decalvans, x-linked MalaCards C0019572 Hairiness C1839161 Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis MalaCards|HPO C1549543 Administration method - pain C0002351 Altitude sickness HSDN C1384666 Decreased hearing C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0012569 Double vision C1443900 Inhalational botulism OrphaNet|MalaCards C0349588 Stature short C1846142 Hoyeraal-hreidarsson syndrome OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0042341 Varicocele HSDN C4084773 Bothered by weight gain C0009651 Conditioning operant HSDN C4084784 Diarrhea C0015408 Eye injury HSDN C0010200 Cough symptom C0014851 Cyst, esophageal HSDN C0031911 Pigment deposition C3495438 Macular degeneration, age-related, 2 MalaCards C0232466 Feeding difficulty C1848578 Methylmalonic aciduria and homocystinuria, cblf type (disorder) MalaCards C0020673 Hypothermia (central) (local) C0011570 Mental depression HSDN C0020305 Fetal edema C2239176 Liver carcinoma HSDN C2911645 Weight loss adverse event C0032226 Pleural diseases HSDN C4085211 Pain distress question C0008370 Cholestasis HSDN C2242996 Tingling C0021308 Infarction HSDN C0018524 Hallucinate C0042909 Vitreous hemorrhage HSDN C4085210 Usual severity pain C0041956 Ureteral obstruction HSDN C4085210 Usual severity pain C0036974 Shock HSDN C2315100 Pediatric failure to thrive C0162666 Mitochondrial encephalomyopathies HSDN C0042928 Paralysis vocal cord C0007222 Cardiovascular diseases HSDN C1384666 Decreased hearing C1861922 Campomelic dysplasia MalaCards|HPO C0018965 Blood urine C2931788 Atypical hemolytic uremic syndrome OrphaNet|MalaCards C0018772 Deafness C0795822 8 rec syndrome OrphaNet|MalaCards C0151827 Pain eye C0000833 Abscess HSDN C4084723 Constipation C1550672 Specimen type - ulcer HSDN C0013911 Emaciate C0005891 Bodies image HSDN C2919142 Short stature adverse event C1969607 Kallmann syndrome 2 with selective tooth agenesis HPO C1962972 Proteinuria adverse event C2673196 Lipoprotein glomerulopathy MalaCards|HPO C0040034 Thrombocytopenia C1855109 Methylmalonic aciduria cbla type HPO C4085211 Pain distress question C1269683 Major depressive disorder HSDN C3815497 Cough C0267830 Pyogenic liver abscess HSDN C0242936 Center pain C0027708 Nephroblastoma HSDN C1963086 Confusion adverse event C0154723 Migraine with aura HSDN C0009676 Confusion state C0029456 Osteoporosis HSDN C0015300 Ocular proptosis C0221356 Brachycephaly OrphaNet|HPO|MalaCards C0020903 Illusion C0012746 Dissociative disorder HSDN C4085211 Pain distress question C0020476 Hyperlipoproteinemias HSDN C0015230 Exanthem C0024788 Green monkey virus disease MalaCards C0009421 Comatose C0017638 Glioma HSDN C1963281 Vomiting adverse event C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency HPO C0036396 Sciatica C0741036 Pns problem UMLS C4085222 Nausea C0018809 Heart neoplasm HSDN C0011991 Loose stools C0035923 German measles vaccine HSDN C2029884 Hearing loss by exam C0022660 Kidney failure, acute HSDN C0036572 Convulsion C0796113 Nephroblastomatosis, fetal ascites, macrosomia and wilms tumor MalaCards C2984058 Have pain C0311375 Arsenic poisoning HSDN C0011991 Loose stools C0697038 Asclepias tuberosa HSDN C2919142 Short stature adverse event C1859298 Spinocerebellar ataxia, autosomal recessive 2 MalaCards|HPO C3463815 Feel fatigue C0036221 Mast-cell sarcoma OrphaNet|MalaCards C0242936 Center pain C0025303 Meningococcal infections HSDN C0010520 Skin cyanosis C0162819 Skin diseases, vascular HSDN C1961131 Cough adverse event C0014858 Esophageal motility disorders HSDN C0003962 Ascites C3554540 Lymphoproliferative syndrome 2 MalaCards C0020673 Hypothermia (central) (local) C0037930 Spinal cord neoplasms HSDN C0151786 Weakness muscle C0021655 Insulin resistance HSDN C0178417 Anhedonia C0236969 Substance-related disorders HSDN C1557397 Adverse event associated with pain C0241158 Cicatrix skin HSDN C0857305 Thrombocytopenia purpura C2586211 Thrombosis of blood vessel HSDN C0011991 Loose stools C0019202 Hepatolenticular degeneration HSDN C0004134 Dyssynergia C0022976 Animal gait disorder HSDN C3274924 Have been coughing C0018916 Hemangioma HSDN C0000737 Abdomen pain C0079770 Lymphoma, small noncleaved-cell MalaCards|HPO C0151889 Reflexes tendon increased C0037769 West syndrome HPO C0917816 Deficiency mental C1866927 Smcr HPO C0575064 Muscle tender C0036231 Sarcocystosis DiseaseOntology C4084768 Usual severity vomiting C0037926 Compression of spinal cord HSDN C1069915 Vertigo C0014038 Encephalitis HSDN C3641756 Have diarrhea C1522137 Hypertriglyceridemia result HSDN C0332563 Papulae C1959582 Pten hamartoma tumor syndrome OrphaNet|MalaCards C0042024 Urine incontinence C0009324 Ulcerative colitis HSDN C0151786 Weakness muscle C0268386 Amyloid polyneuropathy, swiss type MalaCards C0018772 Deafness C1963084 Colitis adverse event HSDN C0151740 Intracranial hypertension C0025284 Meningeal neoplasms MalaCards C0460137 Push down or depress C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C2911645 Weight loss adverse event C0041956 Ureteral obstruction HSDN C0012833 Dizzy C0017181 Gastrointestinal hemorrhage HSDN C1963184 Nystagmus adverse event C0206247 Amyloid neuropathies MalaCards C2055125 Temperature reported over 102 degrees fahrenheit C0014057 Japanese encephalitis DiseaseOntology|MalaCards C0231528 Muscle pain generalized C1835849 Congenital disorder of glycosylation, type im OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0242647 Mucosa-associated lymphoid tissue lymphoma HSDN C4084769 Vomiting frequency C3149848 Variegate porphyria, homozygous variant HPO C4084769 Vomiting frequency C2945560 Hemolytic HSDN C1963093 Dizziness adverse event C0206504 Tympanic membrane perforation HSDN C0018772 Deafness C0796154 Simpson-golabi-behmel syndrome, type 1 MalaCards C0494475 Seizure generalized tonic clonic C0598392 Lennox syndrome MalaCards C0038990 Sweats C0039263 Takayasu arteritis OrphaNet|HPO|MalaCards C4084784 Diarrhea C0007873 Uterine cervical neoplasm HSDN C0240735 Personality change C4225326 Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 UMLS C0010200 Cough symptom C0042075 Urologic diseases HSDN C3539895 Pelvic pain occurs with bowel movement C1000483 Genus anemia HSDN C1145670 Failure respiratory C0265354 Charge syndrome MalaCards|HPO C0020455 Hypergammaglobulinemia C0015467 Neuralgia facial HSDN C3898969 Have been vomiting C1864996 Enteric neuropathy, familial MalaCards C0751837 Gait ataxic C1858391 Ataxia-telangiectasia-like disorder HPO C0009676 Confusion state C0002940 Aneurysm HSDN C0086437 Joint hypermobility C2749127 Primary ovarian insufficiency, fragile x-associated HPO C0150055 Pain chronic C0814263 Meditation therapy HSDN C0030193 Sense of pain C2698017 Cdisc sdtm marital status terminology HSDN C0424755 Fever symptoms C0026936 Mycoplasma infections HSDN C0018681 Headache, cephalalgia C1090821 Sepsis (invertebrate) HSDN C0042928 Paralysis vocal cord C0040149 Subacute thyroiditis HSDN C0018772 Deafness C0270911 Charcot-marie-tooth disease, type ia (disorder) HPO C0000737 Abdomen pain C0037889 Hereditary spherocytosis HSDN C3641756 Have diarrhea C0036231 Sarcocystosis DiseaseOntology C4084784 Diarrhea C0009404 Colorectal neoplasms HSDN C0040034 Thrombocytopenia C1704429 Hypoalphalipoproteinemia, familial MalaCards C2700617 Irritation - emotion C0001231 Acth syndrome, ectopic MalaCards C4084767 Bothered by vomiting C0001768 Agammaglobulinemia HSDN C0857305 Thrombocytopenia purpura C0040028 Thrombocythemia, essential HSDN C1384666 Decreased hearing C0036974 Shock HSDN C0241157 Skin pustule C0406464 Erosive pustular dermatosis of the scalp OrphaNet|MalaCards C0042963 Symptoms vomiting C0029456 Osteoporosis HSDN C4084726 Distress cough C0751674 Lymphangioleiomyomatosis OrphaNet|HSDN|HPO|MalaCards C0242936 Center pain C0019911 Hookworm infections HSDN C0030552 Paralysis partial C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C3641756 Have diarrhea C0030353 Papilledema HSDN C3887784 Decreased urine output C0340629 Aortic aneurysm without mention of rupture nos HSDN C0030193 Sense of pain C0035592 Infection, rickettsiaceae HSDN C0427068 Legs weakness C1970009 Spastic paraplegia 32, autosomal recessive MalaCards C0030554 Abnormal sensation C0007784 Cerebral hemisphere hemorrhage HSDN C1962972 Proteinuria adverse event C0086543 Cataract nos HSDN C0013404 Respiratory difficulty C0016196 Chest flail HSDN C0518090 Frequency of pain question C0011389 Dental plaque HSDN C0036572 Convulsion C0003496 Aortic rupture HSDN C1963252 Tremor adverse event C0268514 Urocanase deficiency MalaCards|HPO C4042891 Sleep wake disorders C0338430 Limbic encephalitis HSDN C0007758 Cerebellar ataxia C0006112 Brain diseases, metabolic HSDN C0085602 Polydypsia C0205734 Diabetes, autoimmune MalaCards C0184566 Comfort alteration C0740697 Psychosocial problem UMLS C0577564 Mass of lymphoreticular structure C1292778 Chronic myeloproliferative disorder UMLS C4085549 Dizziness C0011551 Depersonalisation HSDN C0027796 Neuralgias C0040185 Tibia fracture HSDN C1962972 Proteinuria adverse event C0031046 Pericarditis HSDN C0000737 Abdomen pain C1332552 Bile duct mucoepidermoid carcinoma UMLS C4084774 Have weight loss C0042510 Ventricular fibrillation HSDN C4085862 Bothered by nausea C0036983 Septic shock HSDN C0917816 Deficiency mental C3553937 Pbd4b MalaCards C0015300 Ocular proptosis C0001193 Apert syndrome OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0041341 Tuberous sclerosis HSDN C0010200 Cough symptom C1527298 Dysentery, bacillary HSDN C2984058 Have pain C0029429 Osteochondrosis HSDN C0015672 Decreased energy C0035920 Rubella HSDN C0349588 Stature short C0033300 Progeria OrphaNet|HPO C4084788 Have dizziness C4048184 Trochlear nerve diseases HSDN C0005745 Blepharoptosis C0796113 Nephroblastomatosis, fetal ascites, macrosomia and wilms tumor MalaCards C1962956 Flatulence adverse event C0037072 Diseases sigmoid HSDN C1963252 Tremor adverse event C0036690 Septicemia HSDN C0010038 Corneal opacity disorder C1855840 Hypoparathyroidism-retardation-dysmorphism syndrome MalaCards|HPO C0015672 Decreased energy C0002438 Amebiasis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003827 Art therapies HSDN C1557397 Adverse event associated with pain C0027540 Necrosis HSDN C0027796 Neuralgias C0040034 Thrombocytopenia HSDN C0026838 Spasticity muscle C1999266 Depression adverse event HSDN C0040264 Ear ringing sound C0004352 Autistic disorder HSDN C0030193 Sense of pain C1962974 Chylothorax adverse event HSDN C3829611 Nausea frequency C0011854 Diabetes mellitus, insulin-dependent HSDN C0085593 Chill C0029307 Oroya fever MalaCards C0013911 Emaciate C0027583 Nematode infections HSDN C3463815 Feel fatigue C0270617 Adhesive arachnoiditis MalaCards C4085548 Usual severity dizziness C0037929 Spinal cord injuries HSDN C3539893 Pelvic pain occurs with intercourse C0040136 Thyroid neoplasm HSDN C4042891 Sleep wake disorders C0022410 Joint instability HSDN C0042571 Vertigo subjective C0014544 Epilepsy HSDN C2911647 Weight gain adverse event C1962976 Ventricular fibrillation adverse event HSDN C0423823 Nail thinness C0265428 9p+ syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C1842982 Focal segmental glomerulosclerosis 3, susceptibility to HPO C0030486 Extremity paralysis, lower C0850803 Anaphylaxis (non medication) HSDN C3641756 Have diarrhea C0162316 Iron deficiency anemia HSDN C3829611 Nausea frequency C0003175 Anthrax disease MalaCards C0242670 Chronic vegetative state C0752140 Intracranial embolism HSDN C0038002 Spleen enlargement C0023786 Mucopolysaccharidosis i OrphaNet C0020615 Hypoglycemia nos C0242343 Panhypopituitarism OrphaNet|HPO|MalaCards C0006370 Bulimia C0014038 Encephalitis HSDN C0278152 Hemifacial spasms C0020255 Hydrocephalus HSDN C4084767 Bothered by vomiting C0005944 Metabolic bone disorder HSDN C0522224 Palsied C0008775 Ciguatera poisoning HSDN C1963184 Nystagmus adverse event C3281192 Infantile cerebellar-retinal degeneration MalaCards C0038002 Spleen enlargement C1849236 Severe combined immunodeficiency, atypical HPO C0232726 Tenesmus, rectal C2981236 Stage iii rectosigmoid cancer ajcc v6 UMLS C0349588 Stature short C1866994 Ulnar-mammary syndrome MalaCards C0086437 Joint hypermobility C2751321 Macrocephaly, alopecia, cutis laxa, and scoliosis OrphaNet|HPO C3829611 Nausea frequency C0023676 Life style HSDN C0011991 Loose stools C0036421 Systemic scleroderma HSDN C0040034 Thrombocytopenia C3280026 Hermansky-pudlak syndrome 9 MalaCards C0028081 Night sweat C0855085 Recurrent hodgkin's nodular sclerosis UMLS C2315100 Pediatric failure to thrive C1832661 Anophthalmia and pulmonary hypoplasia MalaCards C3641756 Have diarrhea C0005694 Bladder neck obstruction HSDN C1384666 Decreased hearing C0032285 Pneumonia HSDN C4084766 Vomiting C0206062 Lung diseases, interstitial HSDN C0749870 Upper motor neuron sign C1263846 Attention deficit hyperactivity disorder MalaCards C0018681 Headache, cephalalgia C0024116 Lung diseases, fungal HSDN C2237041 Shox gene with short stature C0342474 Lipoid congenital adrenal hyperplasia OrphaNet C0575081 Abnormal gait C1853154 Nemaline myopathy 7 HPO C0234376 Tremor action C0268525 5-oxoprolinase deficiency MalaCards C2911647 Weight gain adverse event C1963067 Atrial fibrillation adverse event HSDN C0002962 Angina C0001883 Airway obstruction HSDN C0040264 Ear ringing sound C0150277 Meditations HSDN C0009676 Confusion state C0005695 Bladder neoplasm HSDN C0043094 Weight gain C1963138 Hypertension adverse event HSDN C3898969 Have been vomiting C1269683 Major depressive disorder HSDN C0036572 Convulsion C0035333 Retinitis HSDN C1557397 Adverse event associated with pain C0340464 Heartbeats ectopic HSDN C4084767 Bothered by vomiting C0018923 Hemangiosarcoma HSDN C4042891 Sleep wake disorders C0005591 Avian disease HSDN C0015469 Facial paralysis C0007621 Neoplastic cell transformation HSDN C0018784 Deafness sensorineural C3810212 Joubert syndrome 21 MalaCards C0016382 Cutaneous vascular engorgement C0795944 Fountain syndrome MalaCards C0151786 Weakness muscle C0751865 Alcohol-induced disorders, nervous system HSDN C2984057 Have nausea C0037286 Skin neoplasms HSDN C1963184 Nystagmus adverse event C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C0004310 Auditory disorder process C0007959 Charcot-marie-tooth disease HSDN C0009421 Comatose C0597109 Nurse's role HSDN C3463815 Feel fatigue C3714644 Thymus neoplasms MalaCards C1510417 Apraxia of gait C0002395 Alzheimer's disease HSDN C4085661 Usual severity nausea C0042769 Virus diseases HSDN C1963087 Constipation adverse event C0001580 Adolescent behavior HSDN C3163620 Hypotension adverse event C0342200 Endemic cretinism MalaCards C1963065 Apnea adverse event C1861922 Campomelic dysplasia MalaCards|HPO C0036572 Convulsion C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO|UMLS C1549543 Administration method - pain C0015959 Fetomaternal bleeding HSDN C3812171 Bradycardia by ecg finding C3539003 Neuropathy, hereditary sensory and autonomic, type vi MalaCards C2024878 Cardiovascular surgery result: dyspnea C0022822 Hunchback formed after birth HSDN C2315100 Pediatric failure to thrive C0033300 Progeria OrphaNet|HSDN|HPO C0033774 Skin pruritus C0032914 Pre-eclampsia HSDN C0917816 Deficiency mental C2931705 Chromosome 15, distal trisomy 15q OrphaNet|MalaCards C2911645 Weight loss adverse event C1881674 Medical device emits smoke HSDN C0040034 Thrombocytopenia C0393590 Fahr's syndrome (disorder) OrphaNet|HPO|MalaCards C0003079 Pupillary inequality C0007273 Carotid artery diseases HSDN C0018681 Headache, cephalalgia C0019360 Herpes zoster disease DiseaseOntology|MalaCards C2919142 Short stature adverse event C3806742 Colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation MalaCards C0007758 Cerebellar ataxia C0431401 Gillespie syndrome OrphaNet|HPO|MalaCards C0151786 Weakness muscle C1547046 Kind of quantity - taste HSDN C0009398 Color vision defects C0003467 Anxiety HSDN C0424755 Fever symptoms C0162283 Nephrogenic diabetes insipidus OrphaNet|HPO C0011168 Disorder deglutition C1859807 Amyotrophic lateral sclerosis 2, juvenile (disorder) MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0032966 Complication, neoplastic pregnancy HSDN C0232466 Feeding difficulty C0796080 Buenos aires type mental retardation MalaCards C0018520 Breath odor C0016171 Fistula of intestine, excluding rectum and anus HSDN C2242996 Tingling C0022665 Kidney neoplasm HSDN C4085222 Nausea C0042826 Field visual HSDN C4084766 Vomiting C3714644 Thymus neoplasms HSDN C0031911 Pigment deposition C0391816 Tietz syndrome MalaCards C4085210 Usual severity pain C0010403 Cryoglobulinemia HSDN C0000727 Abdomen acute C0013080 Down syndrome HSDN C0917816 Deficiency mental C3711125 Mitochondrial dna depletion syndrome 8a MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0919267 Ovarian neoplasm HSDN C0149651 Clubbing C0264511 Lymphoid interstitial pneumonia MalaCards C0040485 Wryneck C4023354 Abnormality of central motor function UMLS C0013428 Painful urination C0877015 Pelvic organ prolapse HSDN C0015970 Fever unknown origin C0085423 Gram-negative bacterial infections HSDN C0017672 Pain tongue C0036349 Paranoid schizophrenia HSDN C4084776 Weight loss C0007133 Carcinoma, papillary HSDN C0039070 Collapse fleeting C1556682 Adverse event associated with infection HSDN C1145670 Failure respiratory C0023788 Whipple disease MalaCards C2911645 Weight loss adverse event C0153459 Malignant neoplasm of body of pancreas MalaCards C0018524 Hallucinate C0033348 Language program HSDN C4085210 Usual severity pain C0029396 Heterotopic ossification HSDN C0004134 Dyssynergia C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C1963252 Tremor adverse event C2706915 Language:-:point in time:^patient:- HSDN C0036572 Convulsion C0032580 Adenomatous polyposis coli HSDN C1963281 Vomiting adverse event C0009375 Colonic neoplasms HSDN C0750937 Appendicular ataxia C0752123 Spinocerebellar ataxia type 5 HPO C0399590 Drug-induced xerostomia C0043352 Xerostomia UMLS C0234146 Absent reflex C1836916 Posterior column ataxia with retinitis pigmentosa HPO C0042963 Symptoms vomiting C0428977 Bradycardia HSDN C0020505 Excessive eating C0027651 Tumor HSDN C4084767 Bothered by vomiting C0600104 Obsessive compulsive behavior HSDN C4084768 Usual severity vomiting C0919267 Ovarian neoplasm HSDN C0086437 Joint hypermobility C0796279 Carnevale syndrome MalaCards|HPO C0013604 Edematous C0149678 Epstein-barr virus infections HSDN C0042024 Urine incontinence C0559260 Congenital scoliosis HSDN C0557874 Global developmental delay C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria MalaCards C0030193 Sense of pain C3862454 Piriformis syndrome right-sided UMLS C3641755 Have constipation C0376547 Aromatherapy HSDN C0020538 Hbp C1861457 Progressive encephalomyelitis with rigidity MalaCards C4085210 Usual severity pain C0004239 Atrial flutter HSDN C0030193 Sense of pain C0011311 Dengue fever HSDN C3898969 Have been vomiting C1535939 Pneumocystis jiroveci pneumonia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006109 Brain damage, chronic HSDN C0009676 Confusion state C1963198 Pancreatitis adverse event HSDN C0042024 Urine incontinence C0002736 Amyotrophic lateral sclerosis HSDN C0027796 Neuralgias C0005586 Bipolar disorder HSDN C0027498 Nausea vomiting C0795953 Masa syndrome (disorder) MalaCards C0234979 Dysdiadochokinesia C1836694 Striatal degeneration, autosomal dominant OrphaNet|HPO|UMLS C0034151 Hyperglobulinemic purpura C0035435 Rheumatism HSDN C4084774 Have weight loss C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0042940 Disorder of voice C0037397 Behavior social HSDN C0578055 Pain of head and neck region C0575031 Cervical facet syndrome UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0015424 Eyelid neoplasms HSDN C0917816 Deficiency mental C1838611 Male pseudohermaphroditism-mental retardation syndrome, verloes type MalaCards C0030193 Sense of pain C0011428 Dentigerous cyst HSDN C4085317 Diarrhea frequency C0027412 Opioid-related disorders HSDN C4085210 Usual severity pain C0001969 Alcoholic intoxication HSDN C4084723 Constipation C0023470 Myeloid leukemia HSDN C0025287 Meningitis-like C0024198 Lyme disease HSDN C0018777 Deafness, conductive C3537167 Trisomy 21 MalaCards C0423684 Back pain thoracic C0458115 Segmental dysfunction of thoracic region UMLS C0006370 Bulimia C0030319 Panic disorder HSDN C0026821 Cramp C0036420 Localized scleroderma HSDN C0004604 Pain back C0032344 Poisoning aspects HSDN C0270948 Neurogenic muscular atrophy C4015038 Myasthenic syndrome, congenital, 7, presynaptic MalaCards C0002624 Amnesia retrograde C0036344 Schizophrenia, catatonic HSDN C2911645 Weight loss adverse event C0036946 Sheep--diseases HSDN C0022346 Yellow skin C0236969 Substance-related disorders HSDN C0575081 Abnormal gait C0238357 Hyperkalemic periodic paralysis OrphaNet|HPO C0019079 Bloody sputum C0036400 Scimitar syndrome HSDN C0009421 Comatose C0878544 Cardiomyopathies HSDN C0162298 Stiffness joints C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C1963091 Diarrhea adverse event C0023420 Mouse leukemia l1210 HSDN C2984058 Have pain C0282193 Iron overload HSDN C0011991 Loose stools C0019829 Hodgkin disease HSDN C0743973 Fever high C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C2029884 Hearing loss by exam C0017612 Glaucoma, open-angle HSDN C1384666 Decreased hearing C1428293 Slx4 gene HPO C0024031 Back pain lower back C0158298 Other and unspecified back disorders UMLS C0005779 Clotting C0016952 Galactosemias OrphaNet|MalaCards C0151889 Reflexes tendon increased C0039373 Tay-sachs disease OrphaNet|MalaCards C1962956 Flatulence adverse event C0812393 Cancer patients and suicide and depression HSDN C1962972 Proteinuria adverse event C3665623 Serum albumin level decreased below normal HSDN C0085636 Light sensitivity C2931753 Achromatopsia incomplete, x-linked MalaCards|HPO C4084769 Vomiting frequency C0001584 Adolescent psychology HSDN C0010520 Skin cyanosis C1546847 Entity name part type - family HSDN C0917816 Deficiency mental C3151462 Mental retardation, autosomal recessive 14 MalaCards|HPO C2911645 Weight loss adverse event C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse MalaCards C1963071 Back pain adverse event C0001624 Adrenal gland neoplasms HSDN C0018784 Deafness sensorineural C2316212 Cryopyrin-associated periodic syndromes MalaCards C2315100 Pediatric failure to thrive C0282577 Congenital disorders of glycosylation OrphaNet|MalaCards C3665347 Vision impaired C0024796 Marfan syndrome OrphaNet|MalaCards C2984058 Have pain C1535939 Pneumocystis jiroveci pneumonia HSDN C0033377 Caudal displacement C0393946 Myasthenic myopathy MalaCards C4084775 Usual severity weight loss C0566602 Primary sclerosing cholangitis OrphaNet|HPO|MalaCards C0393764 Excessive daytime sleepiness - normal night sleep C0917799 Hypersomnia UMLS C0042940 Disorder of voice C0040409 Tongue diseases HSDN C2911647 Weight gain adverse event C0035455 Rhinitis HSDN C4084776 Weight loss C0011615 Dermatitis, atopic HSDN C1961131 Cough adverse event C0007787 Transient ischemic attack HSDN C3539896 Pelvic pain occurs with urination C0037072 Diseases sigmoid HSDN C0018772 Deafness C1849432 Renal, genital, and middle ear anomalies OrphaNet|MalaCards C3463815 Feel fatigue C0035220 Respiratory distress syndrome, newborn HSDN C1963252 Tremor adverse event C0008066 Child behavior disorders HSDN C2237041 Shox gene with short stature C1859405 Bowen-conradi syndrome OrphaNet|HPO|MalaCards C0027497 Queasy C0032914 Pre-eclampsia HSDN C2984058 Have pain C0015630 Fantasies HSDN C4084766 Vomiting C0220847 C hepatitis virus HSDN C0035455 Rhinitis C3809684 Ciliary dyskinesia, primary, 26 MalaCards C0043094 Weight gain C0043049 Water intoxication HSDN C0026821 Cramp C1548578 Location characteristic id - smoking HSDN C0028738 Nystagmus C0431401 Gillespie syndrome MalaCards C3496180 Sleep apnea C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C0522224 Palsied C0036117 Salmonella infections HSDN C0270948 Neurogenic muscular atrophy C1848533 Ataxia with vitamin e deficiency HPO C0398650 Idiopathic thrombocytopenia purpura C1866120 Autoimmune lymphoproliferative syndrome, type ib MalaCards|HPO C0751495 Seizure focal C0013384 Dyskinetic syndrome MalaCards C0030193 Sense of pain C0085082 Fungemia HSDN C1557397 Adverse event associated with pain C0016079 Figural aftereffects HSDN C0518090 Frequency of pain question C0600041 Infective cystitis HSDN C4084776 Weight loss C0032310 Pneumonia, viral HSDN C4085549 Dizziness C0040038 Thromboembolism HSDN C1963087 Constipation adverse event C0149573 Structure of posterior inferior cerebellar artery HSDN C0015672 Decreased energy C0006118 Brain neoplasms HSDN C0030193 Sense of pain C0034186 Pyelonephritis HSDN C4084773 Bothered by weight gain C0035126 Reperfusion injury HSDN C0003862 Pain joint C0022116 Ischemia HSDN C1557397 Adverse event associated with pain C0001429 Adenolymphoma HSDN C0015300 Ocular proptosis C0265295 Jansen type metaphyseal chondrodysplasia HPO C0022346 Yellow skin C1548578 Location characteristic id - smoking HSDN C1963252 Tremor adverse event C1968550 Mental retardation, x-linked, syndromic 13 MalaCards|HPO C0013395 Indigestion C0042373 Vascular diseases HSDN C0015970 Fever unknown origin C1253937 Pericardial effusion HSDN C1549543 Administration method - pain C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0426579 Anorexia symptom C0035288 Reticuloendotheliosis, x-linked MalaCards C4084775 Usual severity weight loss C0010356 Cross infection HSDN C0031911 Pigment deposition C0038986 Sweat gland diseases MalaCards C4084766 Vomiting C0428977 Bradycardia HSDN C0242936 Center pain C0010035 Hereditary corneal dystrophy HSDN C0039870 Leanness C0026764 Multiple myeloma HSDN C4084784 Diarrhea C0850803 Anaphylaxis (non medication) HSDN C1549543 Administration method - pain C0206504 Tympanic membrane perforation HSDN C4020887 Photodysphoria C0003076 Aniridia OrphaNet C0004604 Pain back C0013926 Aeroembolism HSDN C4085317 Diarrhea frequency C0345904 Malignant neoplasm of liver MalaCards C0497406 Over weight C0009450 Disease caused by microorganism HSDN C4085661 Usual severity nausea C0007138 Carcinoma, transitional cell HSDN C2919142 Short stature adverse event C2931232 Ventricular extrasystoles perodactyly robin sequence MalaCards C0235031 Neurological complaint C1334386 Leptomeningeal melanoma UMLS C0005745 Blepharoptosis C1850597 Leigh syndrome due to mitochondrial complex ii deficiency HPO C2984058 Have pain C0243010 Viral encephalitis HSDN C1962956 Flatulence adverse event C0034884 Rectal fistula HSDN C1961131 Cough adverse event C4015016 Ciliary dyskinesia, primary, 30 MalaCards C1963091 Diarrhea adverse event C0019069 Hemophilia a HSDN C0424755 Fever symptoms C0002875 Cooley's anemia OrphaNet|HPO C4085222 Nausea C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0004134 Dyssynergia C0014536 Epidural tumor HSDN C4084769 Vomiting frequency C0023267 Fibroid tumor HSDN C2024893 Cardiovascular surgery result: fatigue C0021799 Interprofessional relations HSDN C0241137 Skin pallor C0242528 Azotemia HSDN C2165510 Depression accompanied by sleeping less C0011581 Depressive disorder UMLS C0349588 Stature short C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C4084775 Usual severity weight loss C0019069 Hemophilia a HSDN C0004093 Asthenia C0007131 Non-small cell lung carcinoma HSDN C3539892 Pelvic pain in front C0432264 Axial osteosclerosis MalaCards C0009806 Constipate C0042075 Urologic diseases MalaCards C0013604 Edematous C2911643 Encounter due to family history of osteoporosis HSDN C3829611 Nausea frequency C0020649 Hypotension HSDN C1963281 Vomiting adverse event C0018817 Atrial septal defects HSDN C1963065 Apnea adverse event C0034088 Pulmonary valve insufficiency HSDN C0029163 Hemorrhage mouth C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0040259 Tinea pedis C0016436 Folliculitis HSDN C1963091 Diarrhea adverse event C0041974 Urethral stricture HSDN C0518090 Frequency of pain question C0023761 Lip neoplasms HSDN C0030193 Sense of pain C0042076 Urologic neoplasms HSDN C4084769 Vomiting frequency C2984572 Malaria pathway HSDN C0030552 Paralysis partial C1833508 Carnitine palmitoyltransferase ii deficiency, late-onset OrphaNet|HPO C0020672 Body temperature decreased C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0036572 Convulsion C0043379 Xyy karyotype HSDN C0040822 D tremors C1970198 Mental retardation, autosomal recessive 6 HPO C0023530 Leukopenia C0340951 Erythrogenesis imperfecta MalaCards C0030193 Sense of pain C3273727 Breast solid neuroendocrine carcinoma UMLS C0005779 Clotting C1832826 Aplasia cutis congenita, high myopia, and cone-rod dysfunction MalaCards C0017181 Gastrointestinal bleed C1096116 Acquired haemophilia MalaCards C1963154 Renal failure adverse event C0268646 Isolated cystinuria MalaCards C0020438 Hypercalciuria C0029401 Osteitis deformans HSDN C0027498 Nausea vomiting C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0010200 Cough symptom C0751552 Malignant neoplasm of thymus MalaCards C0003811 Cardiac rhythm disturbance C3711749 Nonsyndromic holoprosencephaly MalaCards C0004604 Pain back C0011616 Contact dermatitis HSDN C0000727 Abdomen acute C0016548 Foreign body migration HSDN C0042510 Fibrillation paroxysmal vent C2751830 Long qt syndrome 12 MalaCards|HPO C0522224 Palsied C0031111 Periostitis HSDN C2984058 Have pain C0001618 Tumors of adrenal cortex HSDN C0241457 Tooth cold sensitivity C0011432 Dentin hypersensitivity UMLS C1313952 Periodic breathing C0810021 Other lower respiratory disease UMLS C3665492 Pigmentations C1266113 Leptomeningeal melanocytoma MalaCards C0020458 Hyperhydrosis C0263628 Tumoral calcinosis MalaCards C0747556 Pharyngitis recurrent C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards C1279888 Proteinuria of undiagnosed cause C0017416 Genital neoplasms, female HSDN C0006370 Bulimia C0162703 Pain sensitivity HSDN C0151786 Weakness muscle C0021845 Intestinal perforation HSDN C0011991 Loose stools C0242698 Ventricular dysfunction, left HSDN C0034933 Abnormal reflexes C0520946 Emotional hypersensitivity HSDN C0270844 Convulsions tonic C3150986 Epileptic encephalopathy, early infantile, 7 MalaCards|UMLS C0026821 Cramp C0027651 Tumor HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C2609414 Acute kidney injury HSDN C0015469 Facial paralysis C1837092 Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency HPO C0019572 Hairiness C1412750 Bbs5 gene HPO C0018991 Paralysis one side of body C0014553 Absence epilepsy HSDN C0015672 Decreased energy C0242992 Multiple chemical sensitivity HSDN C0577569 Mass of male genital structure C0153603 Spermatic cord, malignant tumor UMLS C4084723 Constipation C1845902 Fg syndrome 2 MalaCards|HPO C0015970 Fever unknown origin C0151744 Myocardial ischemia HSDN C0031911 Pigment deposition C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C2700617 Irritation - emotion C0038165 Staphylococcal scalded skin syndrome DiseaseOntology|MalaCards C3898969 Have been vomiting C0037198 Sinus thrombosis, intracranial HSDN C3887873 Hearing loss C0236969 Substance-related disorders HSDN C0151786 Weakness muscle C3151853 Mcleod syndrome with chronic granulomatous disease HPO C0037317 Sleep disturbance C0917799 Hypersomnia UMLS C0518090 Frequency of pain question C0038358 Gastric ulcer HSDN C0033774 Skin pruritus C0346104 Follicular atrophoderma and basal cell epitheliomata MalaCards C0476273 Distress respiratory C1867396 Radial-renal syndrome MalaCards C0042025 Urinary incontinence stress C0033377 Ptosis HSDN C0015672 Decreased energy C0017658 Glomerulonephritis HSDN C0033774 Skin pruritus C0033578 Prostatic neoplasms HSDN C0349588 Stature short C2931302 Familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails OrphaNet|MalaCards C4085211 Pain distress question C0276275 Disease due to parvoviridae HSDN C0009792 Consciousness disorder C0007760 Cerebellar diseases HSDN C1961131 Cough adverse event C0013473 Eating disorders HSDN C0038002 Spleen enlargement C3150730 Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency HPO C4085210 Usual severity pain C0085632 Apathy HSDN C0034150 Skin purpura C4084909 Depression subordinate domain HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0015395 Burn eye HSDN C0040822 D tremors C3541306 Plasmodium measurement HSDN C0242936 Center pain C0006818 Campylobacter infection HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0221752 Rbc urine HSDN C0042571 Vertigo subjective C0700501 Congenital nystagmus HSDN C0023014 Developmental disorder language C0997768 Glaucoma HSDN C3815497 Cough C0022810 Disease, kyasanur forest MalaCards C0085593 Chill C0238015 Autonomic dysreflexia UMLS C0000737 Abdomen pain C4084909 Depression subordinate domain HSDN C0557874 Global developmental delay C0039373 Tay-sachs disease OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C3146222 Idiopathic aortitis MalaCards C0233514 Behavior abnormal C1851708 Encephalopathy, recurrent, of childhood MalaCards C4085317 Diarrhea frequency C0043395 Yellow fever OrphaNet|MalaCards C0518090 Frequency of pain question C0023860 Listeriosis HSDN C0030486 Extremity paralysis, lower C0342613 Danish type familial amyloid cardiomyopathy MalaCards C2203646 Jaundice C0018674 Head trauma HSDN C0019572 Hairiness C1837245 Carney complex variant MalaCards C2242996 Tingling C0021843 Intestinal obstruction HSDN C0013390 Cramps menstrual C0018414 Gynatresia HSDN C4084776 Weight loss C0206624 Hepatoblastoma MalaCards C0027497 Queasy C0032227 Pleural effusion disorder HSDN C0009676 Confusion state C0271865 Autoimmune hypoparathyroidism MalaCards C0010038 Corneal opacity disorder C2931646 Oculocerebral hypopigmentation syndrome type preus MalaCards C0006370 Bulimia C0004364 Autoimmune diseases HSDN C0018681 Headache, cephalalgia C0032285 Pneumonia HSDN|UMLS C1557397 Adverse event associated with pain C0178324 Blood vessel injury HSDN C1260880 Nasal drip C2931822 Nasopharyngeal carcinoma UMLS C0020578 Hyperventilate C0013808 Electroconvulsive therapy HSDN C0008031 Pain chest C0812413 Malignant pleural mesothelioma UMLS C4084766 Vomiting C0021359 Infertility HSDN C4084727 Cough frequency C0017612 Glaucoma, open-angle HSDN C0042963 Symptoms vomiting C2981150 Uranostaphyloschisis HSDN C0040264 Ear ringing sound C1853554 Radiation induced meningioma MalaCards C2203646 Jaundice C0340629 Aortic aneurysm without mention of rupture nos HSDN C0036572 Convulsion C3713418 Ppm-x syndrome MalaCards C3665492 Pigmentations C3888065 Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant MalaCards C2024878 Cardiovascular surgery result: dyspnea C0013295 Duodenal ulcer HSDN C0085636 Light sensitivity C1845407 Cone-rod dystrophy, x-linked, 3 HPO C4084774 Have weight loss C0024116 Lung diseases, fungal HSDN C2911647 Weight gain adverse event C0038160 Staphylococcal infections HSDN C0007859 Pain neck C0032285 Pneumonia HSDN C4084775 Usual severity weight loss C0021051 Immunologic deficiency syndromes HSDN C0393766 Postviral excessive daytime sleepiness C0917799 Hypersomnia UMLS C0242936 Center pain C0917875 Esophageal diverticulosis HSDN C0001825 Agraphia C0011581 Depressive disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0008325 Cholecystitis HSDN C4085210 Usual severity pain C0039971 Thirst HSDN C0151825 Ostalgia C0231644 Chest pain xiphodynia UMLS C0577560 Eye mass C0242078 Retina, angiomatosis UMLS C4085210 Usual severity pain C0043119 Werner syndrome HSDN C3463815 Feel fatigue C0020544 Renal hypertension HSDN C0576456 Poor feeding C1837094 Myasthenic syndrome, congenital, ie MalaCards C0020673 Hypothermia (central) (local) C1963064 Anxiety adverse event HSDN C2237041 Shox gene with short stature C3146244 Alcohol related birth defect OrphaNet|MalaCards C4084768 Usual severity vomiting C0013364 Dysautonomia, familial HPO C2984057 Have nausea C0036421 Systemic scleroderma HSDN C4084802 Usual severity diarrhea C0023220 Leg injury HSDN C2919142 Short stature adverse event C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0016724 Froehlich's syndrome HSDN C2024893 Cardiovascular surgery result: fatigue C0279607 Adult primary hepatocellular carcinoma MalaCards C0151740 Intracranial hypertension C0030044 Acrocephaly OrphaNet|HPO|MalaCards C1384666 Decreased hearing C2931928 Mitochondrial cytopathy MalaCards C2919142 Short stature adverse event C2678480 Chromosome 22q11.2 deletion syndrome, distal OrphaNet|HPO|MalaCards C0035078 Failure kidney C0162671 Melas syndrome MalaCards|HPO C0085631 Abnormal excitement C0002736 Amyotrophic lateral sclerosis MalaCards|HPO C2096293 Ent surgical result ear vertigo C0029401 Osteitis deformans HSDN C3463815 Feel fatigue C0018571 Hand injury HSDN C4084766 Vomiting C0751273 Infantile globoid cell leukodystrophy MalaCards C1963281 Vomiting adverse event C0018790 Cardiac arrest HSDN C0398650 Idiopathic thrombocytopenia purpura C1579931 Depressed - symptom HSDN C0037763 Spasm C0264367 Acute bronchiolitis+bron.spasm UMLS C3815497 Cough C0697038 Asclepias tuberosa HSDN C0242936 Center pain C0007871 Uterine cervical incompetence HSDN C0278152 Hemifacial spasms C0152181 Hypoglossal nerve disease or syndrome HSDN C0851578 Disorder sleep C0032962 Pregnancy complications HSDN C0242936 Center pain C0005891 Bodies image HSDN C0027498 Nausea vomiting C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0032763 Post gastrectomy syndrome HSDN C0015469 Facial paralysis C0038356 Stomach neoplasms HSDN C0850758 Pain pelvic C1552262 Nurse practitioner - family HSDN C0454644 Delayed language development C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate OrphaNet|HPO|MalaCards C4085211 Pain distress question C0027859 Acoustic neuroma HSDN C4084766 Vomiting C0031212 Personality disorders HSDN C0035229 Respiratory function impaired C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0011991 Loose stools C0007766 Intracranial aneurysm HSDN C0332563 Papulae C4015128 Porokeratosis 8, disseminated superficial actinic type MalaCards C3463815 Feel fatigue C0022701 Kinesthesia HSDN C0030975 Disorders perception C0004161 Athletic injuries HSDN C0242936 Center pain C0013292 Obstruction duodenal HSDN C0002965 Crescendo angina C0023676 Life style HSDN C0020455 Hypergammaglobulinemia C0007786 Brain ischemia HSDN C0851578 Disorder sleep C0021832 Intestinal diseases, parasitic HSDN C1963184 Nystagmus adverse event C2931391 Cataract mental retardation anal atresia urinary defects OrphaNet|MalaCards C0000727 Abdomen acute C0036690 Septicemia HSDN C0010520 Skin cyanosis C0013182 Drug allergy HSDN C0000737 Abdomen pain C1266018 Hepatocellular carcinoma, scirrhous UMLS C0011206 Delirium acute C0236811 Chronobiology disorders HSDN C4084766 Vomiting C1720777 Functional laterality HSDN C2203646 Jaundice C0037397 Behavior social HSDN C0522224 Palsied C1706377 Memory device component HSDN C0030193 Sense of pain C0039240 Supraventricular tachycardia HSDN C2919142 Short stature adverse event C4015461 Ruijs-aalfs syndrome MalaCards C3539889 Pelvic pain increasing in severity C0221752 Rbc urine HSDN C0860603 Anxiety symptom C0013384 Dyskinetic syndrome MalaCards C0007642 Cellulitis nos C0022739 Klippel-trenaunay-weber syndrome MalaCards C0018926 Emesis bloody C0020875 Ileal diseases HSDN C0004604 Pain back C0017563 Gingival diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006325 Bruxism HSDN C4084767 Bothered by vomiting C0342869 Deficiency of acetyl-coa acyltransferase (disorder) MalaCards C1963137 Hydrocephalus adverse event C0220704 Shprintzen syndrome MalaCards|HPO C2237041 Shox gene with short stature C1853623 Fryns-aftimos syndrome MalaCards C0036572 Convulsion C1318518 Infantile malignant osteopetrosis MalaCards C0578044 Ear painful C0751466 Phonophobia UMLS C0162429 Dietary deficiency C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0036572 Convulsion C3494904 Lennox-gastaut syndrome, non-intractable UMLS C4085317 Diarrhea frequency C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C0018834 Brash C0751667 Canavan disease, juvenile MalaCards C4084776 Weight loss C0242216 Biliary calculi HSDN C1557397 Adverse event associated with pain C0020162 Humerus fracture HSDN C1971624 Appetite absent C0007570 Celiac disease DiseaseOntology C1963071 Back pain adverse event C0017178 Gastrointestinal diseases HSDN C2911647 Weight gain adverse event C0023176 Lead poisoning HSDN C1963067 Atrial fibrillation adverse event C1834481 Cardiomyopathy, dilated, 1s MalaCards C0184567 Pain acute C0043145 Whiplash HSDN C4084776 Weight loss C0022758 Kap HSDN C4085210 Usual severity pain C0034103 Pulpitis HSDN C4084727 Cough frequency C1963067 Atrial fibrillation adverse event HSDN C0746987 Occipital region tender swollen C0362076 Head problem UMLS C2315100 Pediatric failure to thrive C1837329 Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema MalaCards C4084774 Have weight loss C0001815 Primary myelofibrosis HSDN C2919142 Short stature adverse event C1857553 Hsd11b2, arg208cys HPO C2024878 Cardiovascular surgery result: dyspnea C0206093 Neuroectodermal tumors HSDN C4084768 Usual severity vomiting C1856401 Etfa deficiencies HPO C0398650 Idiopathic thrombocytopenia purpura C1956346 Coronary artery disease HSDN C0002962 Angina C0037299 Skin ulcer HSDN C0015468 Face pain C0700327 Clinical findings relating to memory HSDN C1384666 Decreased hearing C1846576 Deafness, autosomal recessive 33 MalaCards C0003862 Pain joint C0019693 Hiv infections HSDN C0522224 Palsied C0036323 Schistosomiasis HSDN C0027497 Queasy C0019080 Hemorrhage HSDN C3539022 Pelvic pain decreasing in severity C0206680 Mesothelioma, cystic HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0024525 Malacoplakia MalaCards C4020887 Photodysphoria C1841721 Achromatopsia 4 HPO C0018989 Paresis of one side of body C0085762 Alcohol abuse UMLS C2024893 Cardiovascular surgery result: fatigue C0151526 Premature birth HSDN C1145670 Failure respiratory C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0011175 Deficient fluid volume C0687720 Central diabetes insipidus OrphaNet|MalaCards C0018772 Deafness C0037579 Soft tissue neoplasms HSDN C4085642 Level of joint stiffness C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C0009421 Comatose C0268569 Intermittent maple syrup urine disease HPO C0150055 Pain chronic C3714514 Infection HSDN C1549543 Administration method - pain C0405580 Adrenal cortical hypofunction HSDN C2219928 Being quick to take offense C0020517 Hypersensitivity UMLS C0020673 Hypothermia (central) (local) C0004943 Behcet syndrome HSDN C2911645 Weight loss adverse event C0004045 Asphyxia neonatorum HSDN C0424755 Fever symptoms C0040427 Tooth abnormalities HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0025268 Multiple endocrine neoplasia type 2a HSDN C0270948 Neurogenic muscular atrophy C0752166 Bardet-biedl syndrome MalaCards|HPO C0013390 Cramps menstrual C0269185 Uterus retroverted HSDN C3541349 Syncope C0340485 Familial ventricular tachycardia MalaCards C3815497 Cough C0007133 Carcinoma, papillary HSDN C0151889 Reflexes tendon increased C1970808 Xeroderma pigmentosum b-cockayne syndrome HPO C0018681 Headache, cephalalgia C0029877 Ear inflammation HSDN C3829611 Nausea frequency C0026857 Musculoskeletal diseases HSDN C0015469 Facial paralysis C0033860 Psoriasis HSDN C2984057 Have nausea C0043121 Wernicke encephalopathy HSDN C1963281 Vomiting adverse event C0003855 Arteriovenous fistula HSDN C4085211 Pain distress question C0035585 Rickettsia infections HSDN C0026826 High muscle tone C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards C0018991 Paralysis one side of body C0038454 Cerebrovascular accident UMLS C4084788 Have dizziness C0022408 Arthropathy HSDN C2919142 Short stature adverse event C0796137 3c syndrome OrphaNet|HPO|MalaCards C4084727 Cough frequency C1299919 Enteric coccidiosis HSDN C4085642 Level of joint stiffness C0079661 Klein's syndrome OrphaNet|HPO|MalaCards C0030486 Extremity paralysis, lower C3244301 Coverage level - family HSDN C0812426 Kidney problem C0748300 Renal failure chronic contrast induced UMLS C0019209 Large liver C1850568 Nakajo syndrome MalaCards|HPO C3146279 Coma C0026269 Mitral valve stenosis HSDN C2984058 Have pain C0015300 Exophthalmos HSDN C1549543 Administration method - pain C0270857 Epilepsy, reflex HSDN C0013604 Edematous C0276275 Disease due to parvoviridae HSDN C0012833 Dizzy C2239176 Liver carcinoma HSDN C0035229 Respiratory function impaired C1332140 Acrofacial dysostosis MalaCards C0042571 Vertigo subjective C0001807 Aggressive behavior HSDN C0030486 Extremity paralysis, lower C0003811 Cardiac arrhythmia HSDN C1963252 Tremor adverse event C1623041 Breast-fed HSDN C0035078 Failure kidney C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0011644 Scleroderma OrphaNet|MalaCards C0015230 Exanthem C4049638 Cutaneous small vessel vasculitis MalaCards C0242936 Center pain C0015556 Fallopian tube diseases HSDN C4085210 Usual severity pain C0751396 Well differentiated oligodendroglioma HSDN C0013404 Respiratory difficulty C0011334 Dental caries HSDN C4085211 Pain distress question C0917875 Esophageal diverticulosis HSDN C3665386 Abnormal vision C1853959 Birdshot chorioretinopathy OrphaNet|HPO|MalaCards C4084725 Usual severity cough C0019284 Diaphragmatic hernia HSDN C0152027 Sensory function defect C0041228 African trypanosomiasis DiseaseOntology C0015469 Facial paralysis C1852502 Craniometaphyseal dysplasia, autosomal dominant HPO C0424755 Fever symptoms C0043253 Trauma blunt HSDN C4084768 Usual severity vomiting C0020522 Delayed hypersensitivity HSDN C0522224 Palsied C0233315 Premature birth of newborn HSDN C0030193 Sense of pain C0038940 Surgical wound dehiscence HSDN C1557397 Adverse event associated with pain C0751396 Well differentiated oligodendroglioma HSDN C0030552 Paralysis partial C0035410 Rhabdomyolysis MalaCards|HSDN C0030794 Pelvis pain C0040136 Thyroid neoplasm HSDN C0011991 Loose stools C0001726 Affective symptoms HSDN C0231528 Muscle pain generalized C3714580 Hypokalemic periodic paralysis type 1 HSDN C0020438 Hypercalciuria C0268080 Hypercalcemia, idiopathic, of infancy HPO C2203646 Jaundice C0007784 Cerebral hemisphere hemorrhage HSDN C0151786 Weakness muscle C0033968 Psychotherapeutic technique HSDN C4084776 Weight loss C0524909 Hepatitis b, chronic HSDN C4084773 Bothered by weight gain C1134719 Invasive ductal breast carcinoma HSDN C4084776 Weight loss C1861848 Paragangliomas 4 MalaCards C0002962 Angina C3469186 Hemochromatosis, type 1 HSDN C1963137 Hydrocephalus adverse event C2674876 Loeys dietz syndrome, type 1b HPO C0151889 Reflexes tendon increased C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0030353 Papilledema HSDN C0010200 Cough symptom C1708653 Laryngeal lymphoepithelial carcinoma UMLS C0424755 Fever symptoms C0041466 Typhoid fever DiseaseOntology|OrphaNet|MalaCards C0577655 Quadricep weakness C0751713 Inclusion body myopathy, sporadic OrphaNet|MalaCards C0000737 Abdomen pain C2987173 Pancreatic solid serous adenoma UMLS C4085210 Usual severity pain C0039263 Takayasu arteritis HSDN C0010200 Cough symptom C0234435 Syncope cough UMLS C0018524 Hallucinate C0042510 Ventricular fibrillation HSDN C0013421 Dystonia C3463992 Epileptic encephalopathy, early infantile, 1 MalaCards C0000731 Abdomen distention C0341480 Pancreas, cyst, congenital MalaCards C2126013 Belching from excessive swallowing of air C0001707 Aerophagia UMLS C0231712 Gait waddling C1836336 Charcot-marie-tooth disease, type 4h MalaCards|HPO|UMLS C0026826 High muscle tone C0795865 Chromosome 17, trisomy 17p OrphaNet|MalaCards C0042024 Urine incontinence C0003125 Anorexia nervosa HSDN C0015300 Ocular proptosis C0265282 Fibrochondrogenesis OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0040799 Traumatic subcutaneous emphysema HSDN C0026838 Spasticity muscle C0004936 Mental disorders HSDN C0000737 Abdomen pain C1832949 Infundibulopelvic dysgenesis MalaCards C2984057 Have nausea C0015802 Femur fracture HSDN C0036659 Sensation disorder C4049994 Insulin resistance measurement HSDN C4085210 Usual severity pain C0039980 Chest injury HSDN C0151908 Dry skin C1567741 Alport syndrome OrphaNet C4084774 Have weight loss C0085407 Infection by cnidospora, nos HSDN C1963066 Joint pain adverse event C3536983 Familial hypophosphatemic rickets MalaCards C1962972 Proteinuria adverse event C0010823 Cytomegalovirus infections HSDN C4084775 Usual severity weight loss C0342623 Senile systemic amyloidosis MalaCards C0151686 Growth retardation C1846421 Lathosterolosis MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0014849 Esophageal and gastric varices HSDN C0232210 Junctional escape beat C0232208 Rhythm nodal UMLS C1963184 Nystagmus adverse event C3550904 Epileptic encephalopathy, early infantile, 36 MalaCards C0015300 Ocular proptosis C1859148 Chondrodysplasia, blomstrand type OrphaNet|HPO|MalaCards C0013604 Edematous C0086543 Cataract nos HSDN C0028738 Nystagmus C0035921 Congenital rubella syndrome OrphaNet|MalaCards C2096293 Ent surgical result ear vertigo C0038160 Staphylococcal infections HSDN C3887873 Hearing loss C0023702 Injury lightning HSDN C0155502 Vertigo benign positional C4050613 Anxiety scale (basc-2) HSDN C1313921 Urinomas C0035078 Kidney failure HSDN C4084725 Usual severity cough C0220981 Metabolic acidosis HSDN C0039070 Collapse fleeting C0001175 Acquired immunodeficiency syndrome HSDN C0018784 Deafness sensorineural C2931667 Fitzsimmons walson mellor syndrome MalaCards C4085210 Usual severity pain C2004493 Leukemia, b-cell HSDN C0751837 Gait ataxic C0206734 Hemangioblastoma HSDN C0030193 Sense of pain C0272375 Antithrombin iii deficiency HSDN C2984057 Have nausea C0305062 Tetanus toxoids HSDN C4084802 Usual severity diarrhea C0037999 Splenic neoplasms HSDN C0026821 Cramp C0585442 Osteosarcoma of bone HSDN C3641755 Have constipation C0021364 Male infertility HSDN C4085548 Usual severity dizziness C2586211 Thrombosis of blood vessel HSDN C0026826 High muscle tone C0033953 Psychosexual disorders HSDN C4084784 Diarrhea C0027726 Nephrotic syndrome HSDN C4085642 Level of joint stiffness C1850168 Bruck syndrome 1 OrphaNet|HPO|MalaCards C0002963 Angina variant C0006118 Brain neoplasms HSDN C0009676 Confusion state C0003850 Arteriosclerosis HSDN C2911647 Weight gain adverse event C0007789 Cerebral palsy HSDN C0150055 Pain chronic C0037929 Spinal cord injuries HSDN C3463815 Feel fatigue C0037274 Dermatologic disorders HSDN C4084724 Usual severity constipation C0036357 Psychology, schizophrenic HSDN C0221752 Rbc urine C0027708 Nephroblastoma HPO C4085210 Usual severity pain C0027849 Neuroleptic malignant syndrome HSDN C0016199 Pain flank C0279937 Cancer of the renal pelvis and ureter, metastatic UMLS C0851578 Disorder sleep C0013504 Echinococcosis, hepatic HSDN C0030552 Paralysis partial C0751254 Creutzfeldt-jakob disease, familial MalaCards C0151889 Reflexes tendon increased C3150707 Chromosome 14q11-q22 deletion syndrome MalaCards C0008031 Pain chest C0007868 Cervical dysplasia UMLS C4084766 Vomiting C1457883 Aggressive reaction HSDN C4084774 Have weight loss C0080179 Vertebra fracture HSDN C0013421 Dystonia C0752109 Brain diseases, metabolic, inborn HSDN C0042798 Vision dim C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C0002962 Angina C2116082 Finding of thyroid nodule by palpation HSDN C0002170 Alopecia disorders C0432291 Mandibuloacral dysostosis OrphaNet|HPO C0520909 Ponv C0020649 Hypotension HSDN C0018681 Headache, cephalalgia C0431118 Choroid plexus meningioma UMLS C4084727 Cough frequency C0041755 Adverse reaction to drug HSDN C1565249 Limitation, mobility C2370841 Convalescence; treatment HSDN C1384666 Decreased hearing C0019562 Von hippel-lindau syndrome MalaCards|HSDN C0428977 Pulse rate decrease C3810401 Atrial standstill 2 MalaCards C4085210 Usual severity pain C0021843 Intestinal obstruction HSDN C1963281 Vomiting adverse event C0015461 Facial neoplasms HSDN C1557397 Adverse event associated with pain C0026613 Motor skills disorders HSDN C0751409 Upper extremity weakness C0520863 Diastolic dysfunction UMLS C0151827 Pain eye C0035320 Retinal neovascularization HSDN C1961131 Cough adverse event C0028796 Dermatitis, occupational HSDN C4085551 Usual severity dry mouth C0265363 Urethral obstruction sequence MalaCards C4085210 Usual severity pain C0020626 Hypoparathyroidism HSDN C0020455 Hypergammaglobulinemia C0018798 Congenital heart defects HSDN C0587047 Mass of trunk C0156397 Vulval hematoma UMLS C0008031 Pain chest C0011581 Depressive disorder HSDN C0026838 Spasticity muscle C0206245 Amyloid neuropathies, familial MalaCards C3887638 Failure to thrive in infant C1869122 Ehlers-danlos syndrome, progeroid form HPO C0004134 Dyssynergia C0685837 Pure gonadal dysgenesis, 46, xx HPO C1963252 Tremor adverse event C0031485 Phenylketonurias HSDN C0231528 Muscle pain generalized C0340708 Lower extremity deep venous thrombosis UMLS C0151786 Weakness muscle C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0040822 D tremors C2015933 Outcomes otolaryngology hearing HSDN C0030552 Paralysis partial C2931902 Acute brachial neuritis MalaCards C4084725 Usual severity cough C3714644 Thymus neoplasms OrphaNet|MalaCards C4084727 Cough frequency C0026266 Mitral valve insufficiency HSDN C4085642 Level of joint stiffness C0220765 Weaver-like syndrome MalaCards C0018772 Deafness C1548484 Rheumatic fever vaccine HSDN C4085222 Nausea C1963107 Euphoria adverse event HSDN C2237041 Shox gene with short stature C4015513 Myopathy, isolated mitochondrial, autosomal dominant MalaCards C0007758 Cerebellar ataxia C0029294 Orofaciodigital syndromes MalaCards C0015469 Facial paralysis C1853926 Nonaka myopathy MalaCards|HPO C0015672 Decreased energy C0814263 Meditation therapy HSDN C4085661 Usual severity nausea C3839212 Familial hyperaldosteronism type 2 MalaCards C0030193 Sense of pain C0022610 Kernicterus HSDN C0020505 Excessive eating C0376154 Skin callus HSDN C3665347 Vision impaired C0039373 Tay-sachs disease OrphaNet|MalaCards C0237326 Defecation pain C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C0041834 Erythematous condition C0392784 Dermatofibrosarcoma protuberans OrphaNet|HPO|MalaCards C4085222 Nausea C0025281 Meniere disease HSDN C0497406 Over weight C0043046 Wasting syndrome HSDN C4085211 Pain distress question C0007772 Intracranial arteriovenous malformation HSDN C0004941 Behavioral symptoms C0015923 Fetal alcohol syndrome OrphaNet|MalaCards C0013404 Respiratory difficulty C0221757 Alpha 1-antitrypsin deficiency HPO C0151311 Cranial nerve palsy C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C0424755 Fever symptoms C0032580 Adenomatous polyposis coli HSDN C0013395 Indigestion C0022758 Kap HSDN C0518090 Frequency of pain question C0008073 Developmental disabilities HSDN C1963137 Hydrocephalus adverse event C0342543 Precocious puberty, central MalaCards C4084727 Cough frequency C0011853 Diabetes mellitus, experimental HSDN C1963137 Hydrocephalus adverse event C0796137 3c syndrome OrphaNet|HPO|MalaCards C0237326 Defecation pain C1855849 Bartter syndrome, antenatal , type 2 HPO C3641756 Have diarrhea C3495801 Granulomatosis with polyangiitis HSDN C1963091 Diarrhea adverse event C0006145 Breast diseases HSDN C0424755 Fever symptoms C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C0271215 Blindness legal C1838979 Mitochondrial complex i deficiency MalaCards|HPO C1963091 Diarrhea adverse event C0008628 Chromosome deletion HSDN C0026821 Cramp C0079744 Diffuse large b-cell lymphoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0017658 Glomerulonephritis HSDN C0002962 Angina C0007772 Intracranial arteriovenous malformation HSDN C3641756 Have diarrhea C0039336 Gustatory sense HSDN C2096293 Ent surgical result ear vertigo C0017601 Glaucomas HSDN C0557874 Global developmental delay C1850053 Pelizaeus-merzbacher-like disease, autosomal recessive, 2 MalaCards|HPO C0518090 Frequency of pain question C0311277 Obesity, abdominal HSDN C4084776 Weight loss C0021280 Infant nutrition disorder HSDN C0013404 Respiratory difficulty C0032787 Postoperative complications HSDN C4084788 Have dizziness C0034186 Pyelonephritis HSDN C3463815 Feel fatigue C0031511 Pheochromocytoma MalaCards|HSDN C0085636 Light sensitivity C0750929 Arnold-chiari malformation, type i MalaCards|UMLS C2013427 Oral cavity symptoms C0149745 Oral ulcer UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C0153257 Coccidioidomycosis primary pulmonary MalaCards C4084724 Usual severity constipation C0007873 Uterine cervical neoplasm HSDN C0030193 Sense of pain C0206660 Germinoma HSDN C4085210 Usual severity pain C1691215 Penile hypospadias HSDN C2919142 Short stature adverse event C1835172 Congenital hypomelanotic and hypermelanotic macules OrphaNet|MalaCards C3714552 Strength decreased C0410226 Congenital myotonic dystrophy MalaCards C2024878 Cardiovascular surgery result: dyspnea C1861984 Cardiac conduction defect, nonprogressive HPO C0085631 Abnormal excitement C0033046 Premenstrual syndrome HSDN C0019209 Large liver C2675526 Neutropenia, severe congenital, autosomal recessive 4 HPO C2024893 Cardiovascular surgery result: fatigue C1956390 Cranial arteritis MalaCards C0018784 Deafness sensorineural C0559260 Congenital scoliosis HSDN C0424755 Fever symptoms C0242383 Age related macular degeneration HSDN C4049644 Depression C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0003624 Appetitive behavior HSDN C3539889 Pelvic pain increasing in severity C0520946 Emotional hypersensitivity HSDN C4084775 Usual severity weight loss C0020544 Renal hypertension HSDN C0522224 Palsied C0005967 Bone neoplasms HSDN C0860603 Anxiety symptom C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0027498 Nausea vomiting C0268581 Holocarboxylase synthetase deficiency OrphaNet|HPO|MalaCards C0857305 Thrombocytopenia purpura C0006663 Calcinosis HSDN C0851578 Disorder sleep C0007193 Cardiomyopathy, dilated HSDN C1963086 Confusion adverse event C0152054 Therapeutic touch HSDN C4085661 Usual severity nausea C0023530 Leukopenia HSDN C0221752 Rbc urine C0002986 Fabry disease OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0035229 Respiratory insufficiency HSDN C4084723 Constipation C0027663 Neoplasms, multiple primary HSDN C0009398 Color vision defects C0220701 Retinitis pigmentosa 1 MalaCards C4084773 Bothered by weight gain C1553188 Hemolysis - observation HSDN C0013404 Respiratory difficulty C3495422 Finding relating to sexuality and sexual activity HSDN C2024878 Cardiovascular surgery result: dyspnea C0003499 Supravalvular aortic stenosis HSDN C0085636 Light sensitivity C0039132 Cutaneous syphilis HSDN C3539896 Pelvic pain occurs with urination C0751792 Trauma, nervous system HSDN C1963281 Vomiting adverse event C1550639 Specimen type - fistula HSDN C4084768 Usual severity vomiting C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C3463815 Feel fatigue C0524620 Metabolic syndrome x HSDN C0270948 Neurogenic muscular atrophy C0751713 Inclusion body myopathy, sporadic OrphaNet|MalaCards C4020887 Photodysphoria C1837873 Leber congenital amaurosis 9 (disorder) MalaCards|HPO C0000737 Abdomen pain C0023869 Lithiasis HSDN C3887638 Failure to thrive in infant C3244301 Coverage level - family HSDN C1963252 Tremor adverse event C0026764 Multiple myeloma HSDN C2237041 Shox gene with short stature C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C0003469 Anxiety disorder C2931205 Usher syndrome, type 1a MalaCards C0312416 Morning sickness C0035317 Retinal hemorrhage HSDN C3539023 Pelvic pain increasing in frequency C1458155 Mammary neoplasms HSDN C0424755 Fever symptoms C1261473 Sarcoma HSDN C0036572 Convulsion C0278193 Reading epilepsy MalaCards|UMLS C0043094 Weight gain C0600518 Choroidal neovascularization HSDN C0030554 Abnormal sensation C1548578 Location characteristic id - smoking HSDN C0042928 Paralysis vocal cord C3714514 Infection HSDN C0007859 Pain neck C0040997 Trigeminal neuralgia HSDN C1069915 Vertigo C0011616 Contact dermatitis HSDN C0004134 Dyssynergia C0010346 Crohn disease HSDN C3887784 Decreased urine output C0041364 Tumor lysis syndrome HSDN C0151786 Weakness muscle C0877149 Pain patellofemoral syndrome HSDN C2237041 Shox gene with short stature C0032897 Prader-willi syndrome OrphaNet|HPO|MalaCards C0038506 Stutter C0026650 Movement disorders HSDN C0518090 Frequency of pain question C1527298 Dysentery, bacillary HSDN C4085222 Nausea C0078981 Arachnoid cysts HSDN C0013604 Edematous C0024421 Macroglossia HSDN C0917816 Deficiency mental C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO C1384666 Decreased hearing C2931196 Craniofacial dysostosis type 1 MalaCards C0006277 Bronchitis C0340037 Young syndrome MalaCards C0026838 Spasticity muscle C0238015 Autonomic dysreflexia HSDN C4042891 Sleep wake disorders C0011882 Diabetic neuropathies HSDN C0020578 Hyperventilate C1419157 Pygm gene HSDN C0013395 Indigestion C0027686 Pathologic neovascularization HSDN C4084769 Vomiting frequency C0037274 Dermatologic disorders HSDN C0015676 Mental fatigue C0520679 Sleep apnea, obstructive HSDN C0011991 Loose stools C0032964 Pregnancy complications, hematologic HSDN C2911645 Weight loss adverse event C0024116 Lung diseases, fungal HSDN C0036572 Convulsion C0023066 Laryngismus HSDN C3887638 Failure to thrive in infant C0268130 Hereditary orotic aciduria, type 1 MalaCards C0030193 Sense of pain C0019284 Diaphragmatic hernia HSDN C0015468 Face pain C0007462 Causalgia syndrome HSDN C0242936 Center pain C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C0036572 Convulsion C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0476273 Distress respiratory C0025229 Melioidosis DiseaseOntology|MalaCards C0241165 Skin thickening C3891556 Chromosome xq26.3 duplication syndrome MalaCards|UMLS C2242996 Tingling C2937358 Cerebral hemorrhage HSDN C0019079 Bloody sputum C0453996 Tobacco smoking HSDN C4084774 Have weight loss C0205788 Histiocytoid hemangioma HSDN C2237041 Shox gene with short stature C3809431 Microcephaly 11, primary, autosomal recessive MalaCards C4084774 Have weight loss C0003504 Aortic valve insufficiency HSDN C0018681 Headache, cephalalgia C2984291 Glioblastoma multiforme pathway HSDN C3541349 Syncope C0019080 Hemorrhage HSDN C0040485 Wryneck C0878682 Ceruloplasmin deficiency OrphaNet|UMLS|HPO|MalaCards C1962956 Flatulence adverse event C0237873 Physiological sexual disorders HSDN C3541349 Syncope C0949658 Cardiomyopathy, hypertrophic, familial HSDN C0557874 Global developmental delay C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C1963137 Hydrocephalus adverse event C2931219 Dysmorphic facial features and multiple structural abnormalities MalaCards C0011991 Loose stools C1855057 Ataxia-telangiectasia variant v2 HPO C0036572 Convulsion C1522475 Intradermal route of drug administration HSDN C0022346 Yellow skin C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards|UMLS C3641756 Have diarrhea C0021847 Intestinal pseudo-obstruction HSDN C0917816 Deficiency mental C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C0011991 Loose stools C0032460 Polycystic ovary syndrome HSDN C0037763 Spasm C0003850 Arteriosclerosis HSDN C0019209 Large liver C0398738 Leukocyte adhesion deficiency type 1 MalaCards C0024312 Lymphocytopenia C1274233 T-lymphocyte immunodeficiency MalaCards C4084727 Cough frequency C0004610 Bacteremia HSDN C0042514 Ventricular tachycardia C3810138 Arrhythmogenic right ventricular dysplasia, familial, 13 MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0023903 Liver neoplasms HSDN C0041657 Consciousness loss C0524812 Intracranial hypotension HSDN C1557397 Adverse event associated with pain C0035235 Respiratory syncytial virus infections HSDN C4084776 Weight loss C0008728 Churg-strauss syndrome OrphaNet|MalaCards C0034933 Abnormal reflexes C0796561 Melanoma vaccines HSDN C1963091 Diarrhea adverse event C0012819 Diverticular disease of colon HSDN C0026826 High muscle tone C1970253 Phosphoserine aminotransferase deficiency MalaCards|HPO C0349506 Sun sensitivity C2931197 Waaler aarskog syndrome MalaCards C1962972 Proteinuria adverse event C0021933 Intussusception HSDN C3541349 Syncope C0007097 Carcinomas HSDN C0037763 Spasm C0237873 Physiological sexual disorders HSDN C1963281 Vomiting adverse event C0035335 Retinoblastoma HSDN C0151786 Weakness muscle C0011849 Diabetes mellitus HSDN C2984058 Have pain C0040156 Thyrotoxicosis HSDN C0030193 Sense of pain C0031111 Periostitis HSDN C0332573 Macula C0346037 Acral lentiginous malignant melanoma UMLS C0557874 Global developmental delay C0751667 Canavan disease, juvenile MalaCards C4084727 Cough frequency C1546533 Specimen source codes - abscess HSDN C0393588 Dystonias paroxysmal C1842531 Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp MalaCards C0040822 D tremors C0011854 Diabetes mellitus, insulin-dependent HSDN C0033774 Skin pruritus C0031090 Periodontal diseases HSDN C0041657 Consciousness loss C0038160 Staphylococcal infections HSDN C0010520 Skin cyanosis C0018800 Cardiomegaly HSDN C0018784 Deafness sensorineural C1510412 Pseudoaneurysm HSDN C0018784 Deafness sensorineural C0236969 Substance-related disorders HSDN C4084773 Bothered by weight gain C0010418 Cryptosporidiosis HSDN C2024893 Cardiovascular surgery result: fatigue C1962983 Cataract adverse event HSDN C0036572 Convulsion C0015414 Eye neoplasms HSDN C0020505 Excessive eating C1848030 Hypotonia-cystinuria syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C0024620 Primary malignant neoplasm of liver MalaCards C4085222 Nausea C0014544 Epilepsy HSDN C0027796 Neuralgias C0015695 Fatty liver HSDN C0013404 Respiratory difficulty C0030354 Papilloma HSDN C3541349 Syncope C0025281 Meniere disease HSDN C0013421 Dystonia C0013806 Electroplexy shock therapy HSDN C3641755 Have constipation C1963067 Atrial fibrillation adverse event HSDN C0018772 Deafness C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO C0023012 Delay language C0268553 Hyperlysinemias HPO C0013404 Respiratory difficulty C3810212 Joubert syndrome 21 MalaCards|UMLS C0042798 Vision dim C2751812 Optic atrophy 7 (disorder) HPO C1963090 Dehydration adverse event C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO C0020673 Hypothermia (central) (local) C0002895 Anemia, sickle cell HSDN C2024893 Cardiovascular surgery result: fatigue C1090821 Sepsis (invertebrate) HSDN C0036572 Convulsion C0005119 Bereavement HSDN C0750394 Wbc low C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C0000737 Abdomen pain C0002736 Amyotrophic lateral sclerosis HSDN C0037036 Increased salivation C1263846 Attention deficit hyperactivity disorder MalaCards C1384666 Decreased hearing C0004304 Auditory fatigue HSDN C0428977 Pulse rate decrease C1563716 Thyroid dysgenesis HPO C4085210 Usual severity pain C0007140 Carcinosarcoma HSDN C4084723 Constipation C0003838 Arterial occlusive diseases HSDN C0344434 Atrial fibrillation ecg C2678477 Brugada syndrome 4 MalaCards|HPO C4049644 Depression C0002986 Fabry disease MalaCards|HPO C3887873 Hearing loss C0013990 Pathological accumulation of air in tissues HSDN C3665492 Pigmentations C0004114 Astrocytoma MalaCards C0027066 Myoclonic jerking C3280977 Spastic ataxia 5, autosomal recessive UMLS C4042891 Sleep wake disorders C0007786 Brain ischemia HSDN C0036572 Convulsion C1837819 Cerebrofrontofacial syndrome MalaCards C0040822 D tremors C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards|UMLS C0030975 Disorders perception C1457883 Aggressive reaction HSDN C0518090 Frequency of pain question C0006281 Congenital bronchogenic cyst HSDN C3146279 Coma C1855371 Maple syrup urine disease, type ii HPO C0023380 Lethargy C1707400 Classic medulloblastoma MalaCards C0020580 Decreased sensation C0221065 Subacute combined degeneration HSDN C1963281 Vomiting adverse event C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0018772 Deafness C0029408 Degenerative polyarthritis HSDN C0007859 Pain neck C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0041327 Tuberculosis, pulmonary HSDN C0003467 Angst C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C4085211 Pain distress question C0423772 Cutaneous fistula HSDN C4085210 Usual severity pain C0036205 Sarcoidosis, pulmonary HSDN C0848203 Male pelvic pain C0453996 Tobacco smoking HSDN C2315100 Pediatric failure to thrive C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C0018772 Deafness C0002878 Anemia, hemolytic HSDN C0024031 Back pain lower back C0032708 Disorders of porphyrin metabolism HSDN C1549543 Administration method - pain C0016124 Finger injury HSDN C0026838 Spasticity muscle C0029534 Other cerebellar ataxia MalaCards C0344434 Atrial fibrillation ecg C2678484 Long qt syndrome 10 HPO C0542476 Forgetful C0003467 Anxiety UMLS C1963281 Vomiting adverse event C0016483 Food preferences HSDN C0043094 Weight gain C0162871 Aortic aneurysm, abdominal HSDN C0030486 Extremity paralysis, lower C1290398 Cerebral arterial aneurysm HSDN C0019209 Large liver C1291560 Deficiency of glutamate decarboxylase MalaCards|HPO C3463815 Feel fatigue C0549567 Pigmentation disorders HSDN C2911645 Weight loss adverse event C3887662 Intraspinal neoplasm HSDN C0008031 Pain chest C0017653 Glomus tumor HSDN C0234132 Pyramidal sign C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards C0020639 Hypoproteinaemia C1859753 Acc with intestinal lymphangiectasia OrphaNet|MalaCards C1836296 Lower extremity weakness C0027577 Nelson syndrome OrphaNet|MalaCards C0018772 Deafness C0005940 Bone diseases HSDN C4084767 Bothered by vomiting C0028738 Nystagmus HSDN C1549543 Administration method - pain C0036830 Serum sickness HSDN C0026821 Cramp C0020473 Hyperlipidemia HSDN C0027066 Myoclonic jerking C1864723 Pyridoxamine 5-prime-phosphate oxidase deficiency HPO|UMLS C0391860 Diffuse inflammations C0264477 Grain-handler's disease UMLS C0242936 Center pain C1136321 Hiv-associated lipodystrophy syndrome HSDN C2984058 Have pain C0751772 Rem sleep behavior disorder HSDN C0030486 Extremity paralysis, lower C0032964 Pregnancy complications, hematologic HSDN C0460137 Push down or depress C1864112 Huntington disease-like 1 MalaCards|HPO C4085317 Diarrhea frequency C0311375 Arsenic poisoning HSDN C0162298 Stiffness joints C1834674 Bethlem myopathy OrphaNet|HPO|MalaCards C0040034 Thrombocytopenia C1842763 Spondyloenchondrodysplasia with immune dysregulation MalaCards C0013395 Indigestion C1868916 Gastroesophageal burning UMLS C0030232 Color loss C0035334 Retinitis pigmentosa HSDN C0003467 Angst C0544012 Aberfeld's syndrome MalaCards C0018681 Headache, cephalalgia C0027531 Neck injury HSDN C0030193 Sense of pain C1334675 Mediastinal extraskeletal osteosarcoma UMLS C0012833 Dizzy C0270860 Basilar-type migraine UMLS C1971624 Appetite absent C0153463 Malig neop oth spec pancreas MalaCards C2911645 Weight loss adverse event C1334374 Laryngeal neuroendocrine neoplasm MalaCards C3541349 Syncope C0264886 Conduction disorder of the heart MalaCards C0151786 Weakness muscle C0342642 Autosomal dominant hypophosphatemic rickets OrphaNet|HPO|MalaCards C0746674 Muscle weakness generalized C0810058 Other connective tissue disease UMLS C4084727 Cough frequency C0021400 Influenza DiseaseOntology|MalaCards C0030193 Sense of pain C1519207 Sebaceous breast carcinoma UMLS C1963063 Anorexia adverse event C0005967 Bone neoplasms HSDN C4084774 Have weight loss C2931242 Familial waldmann's disease MalaCards C0027498 Nausea vomiting C0745138 Hypertensive urgency UMLS C0036572 Convulsion C1854989 Molybdenum cofactor deficiency, complementation group b HPO C1069915 Vertigo C0006663 Calcinosis HSDN C1963091 Diarrhea adverse event C0039520 Tenosynovitis HSDN C4084724 Usual severity constipation C0033246 Proctitis HSDN C0349588 Stature short C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C4085317 Diarrhea frequency C0029106 Opisthorchiasis DiseaseOntology C1510417 Apraxia of gait C1510428 Cerebral abscess HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032372 Poliomyelitis, anterior, acute HSDN C0025874 Uterine bleeding dysfunctional C0010481 Cushing syndrome OrphaNet|HPO C0002962 Angina C0036429 Sclerosis HSDN C2984058 Have pain C0018128 Graft occlusion, vascular HSDN C0009421 Comatose C0014077 Leukoencephalitis, acute hemorrhagic HSDN C0557874 Global developmental delay C0268131 Omp decarboxylase deficiency MalaCards C0020578 Hyperventilate C0007774 Cerebral arterial diseases HSDN C3887638 Failure to thrive in infant C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency MalaCards C0035078 Failure kidney C0473583 Nevus elasticus MalaCards C0040264 Ear ringing sound C0036974 Shock HSDN C0030554 Abnormal sensation C0007131 Non-small cell lung carcinoma HSDN C2919142 Short stature adverse event C0152416 Congenital web of larynx OrphaNet|MalaCards C0027497 Queasy C3714514 Infection HSDN C1384666 Decreased hearing C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C0020458 Hyperhydrosis C3203358 Hypoventilation MalaCards C0013404 Respiratory difficulty C0007134 Renal cell carcinoma HSDN C2165511 Depression accompanied by sleeping more C0917799 Hypersomnia UMLS C0009792 Consciousness disorder C0034088 Pulmonary valve insufficiency HSDN C0009806 Constipate C0085073 Prosthesis-related infection HSDN C0036659 Sensation disorder C0010054 Coronary arteriosclerosis HSDN C0018926 Emesis bloody C1579931 Depressed - symptom HSDN C3887638 Failure to thrive in infant C0010674 Cystic fibrosis MalaCards|HPO C2700617 Irritation - emotion C0268412 Infantile hypophosphatasia MalaCards|HPO C0332563 Papulae C1860167 Ackerman syndrome MalaCards C4084726 Distress cough C0032319 Pneumopericardium HSDN C0022346 Yellow skin C3241945 Melena due to gastrointestinal hemorrhage HSDN C2936821 Spinal cerebrospinal fluid leak C0028433 Nose neoplasms HSDN C1963063 Anorexia adverse event C3495422 Finding relating to sexuality and sexual activity HSDN C4084776 Weight loss C2984572 Malaria pathway HSDN C0000737 Abdomen pain C1832940 Juvenile polyposis of stomach HPO C0020903 Illusion C0007766 Intracranial aneurysm HSDN C4085210 Usual severity pain C0009442 Common bile duct neoplasms HSDN C2242996 Tingling C0038587 Substance withdrawal syndrome HSDN C0013404 Respiratory difficulty C0149931 Migraine disorders HSDN C0000737 Abdomen pain C1332527 Benign ovarian serous neoplasm UMLS C2984058 Have pain C0012655 Disease susceptibility HSDN C0003811 Cardiac rhythm disturbance C1859967 Agonadism dextrocardia diaphragmatic hernia MalaCards C0085650 Purpura fulminans C0010403 Cryoglobulinemia HSDN C0231218 Malaise generalized C3899977 Bclc stage c hepatocellular carcinoma UMLS C0427068 Legs weakness C0349604 Intracranial meningioma MalaCards C0035078 Failure kidney C1857423 Cystic kidney disease with ventriculomegaly MalaCards|HPO C0020672 Body temperature decreased C0013928 Fat embolism HSDN C0521991 Stress symptom C2957419 Military combat stress reaction UMLS C1546759 Specimen source codes - pustule C3280501 Inflammatory skin and bowel disease, neonatal, 1 MalaCards C0009676 Confusion state C0520946 Emotional hypersensitivity HSDN C0012569 Double vision C0022363 Jaw fracture HSDN C4049644 Depression C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C4084776 Weight loss C0023267 Fibroid tumor HSDN C4085317 Diarrhea frequency C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C0042940 Disorder of voice C0037369 Smoking HSDN C1145670 Failure respiratory C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C1853297 Maturity-onset diabetes of the young, type 8, with exocrine dysfunction UMLS C4084725 Usual severity cough C0023890 Liver cirrhosis HSDN C4085210 Usual severity pain C0028242 Nocardia infections HSDN C2024893 Cardiovascular surgery result: fatigue C0021345 Infectious mononucleosis DiseaseOntology|HSDN C0011570 Monopolar depression C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C4084768 Usual severity vomiting C0751273 Infantile globoid cell leukodystrophy MalaCards C0017565 Gingiva hemorrhage C0268250 Gaucher disease, type 2 (disorder) MalaCards C0700072 Encounter due to stillbirth C1842704 Gaucher disease, perinatal lethal OrphaNet|HPO|MalaCards C4085211 Pain distress question C0025064 Mediastinitis HSDN C4084775 Usual severity weight loss C2931876 Hirschsprung disease 1 MalaCards C3274924 Have been coughing C0036467 Scrofula MalaCards C0221263 Cafe au lait spot C0041341 Tuberous sclerosis HPO C4084775 Usual severity weight loss C2117118 X-ray of toe: deformity contracture HSDN C0009024 Clonus C0268540 Hhh syndrome HPO|UMLS C4050613 Anxiety C0220704 Shprintzen syndrome MalaCards|HPO C0085631 Abnormal excitement C0014859 Esophageal neoplasms HSDN C0242936 Center pain C0025281 Meniere disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0006147 Breast fed HSDN C3641756 Have diarrhea C1705714 Lats1 wt allele HSDN C2919142 Short stature adverse event C2748572 Sesame syndrome HPO C0917816 Deficiency mental C4053775 Pituitary stalk interruption syndrome MalaCards C1557397 Adverse event associated with pain C0206654 Leiomyomatosis HSDN C1963063 Anorexia adverse event C0021280 Infant nutrition disorder HSDN C0426579 Anorexia symptom C0235782 Gallbladder carcinoma OrphaNet C0015469 Facial paralysis C1834014 Oculopharyngodistal myopathy MalaCards C0026821 Cramp C1579931 Depressed - symptom HSDN C1557397 Adverse event associated with pain C0001420 Papillary adenocarcinoma HSDN C0003469 Anxiety disorder C1834570 Myoclonic dystonia HPO C3665347 Vision impaired C0271092 Progressive cone dystrophy (without rod involvement) OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0037299 Skin ulcer HSDN C0151889 Reflexes tendon increased C0795953 Masa syndrome (disorder) OrphaNet|HPO|MalaCards C0015732 Feces incontinence C0238357 Hyperkalemic periodic paralysis HPO C0231528 Muscle pain generalized C0038041 Spotted fevers DiseaseOntology|MalaCards C0150055 Pain chronic C0178282 Hernia of abdominal cavity HSDN C0018784 Deafness sensorineural C0007133 Carcinoma, papillary HSDN C4084775 Usual severity weight loss C0001144 Acne vulgaris HSDN C0426579 Anorexia symptom C1552962 Units of measure - pica HSDN C0013404 Respiratory difficulty C0017181 Gastrointestinal hemorrhage HSDN C1963091 Diarrhea adverse event C0025268 Multiple endocrine neoplasia type 2a OrphaNet C4084727 Cough frequency C0009917 Contracture HSDN C0002170 Alopecia disorders C0796002 Johnson-mcmillin syndrome MalaCards C3539890 Pelvic pain causes awakening at night C0006434 Burn injury HSDN C1963086 Confusion adverse event C0520946 Emotional hypersensitivity HSDN C2984058 Have pain C0041309 Tuberculosis, cutaneous HSDN C0231528 Muscle pain generalized C0086922 Purpura rheumatoid OrphaNet|MalaCards C0015469 Facial paralysis C1290398 Cerebral arterial aneurysm HSDN C3887638 Failure to thrive in infant C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C0010200 Cough symptom C1322286 Thymoma, type c OrphaNet|MalaCards C3463815 Feel fatigue C1334968 Nodular lymphocyte predominant hodgkin lymphoma MalaCards C0011206 Delirium acute C0032019 Pituitary neoplasms HSDN C1961131 Cough adverse event C0023240 Legionellosis OrphaNet|MalaCards C1963087 Constipation adverse event C0853697 Neutrophil count decreased HSDN C1836296 Lower extremity weakness C2828721 Spastic paraplegia 46, autosomal recessive MalaCards|UMLS C0026838 Spasticity muscle C3280977 Spastic ataxia 5, autosomal recessive UMLS C0030552 Paralysis partial C0041330 Tuberculosis, spinal HSDN C4084769 Vomiting frequency C2717979 Tooth wear HSDN C1510456 Wernicke aphasia C3714639 Exit block by ecg finding HSDN C3815497 Cough C0013926 Aeroembolism HSDN C0042963 Symptoms vomiting C0001882 Air sickness UMLS C0018991 Paralysis one side of body C1546602 Specimen source codes - diverticulum HSDN C0339251 Blood pigmentation of cornea C0151571 Lesion corneal UMLS C0020538 Hbp C0032339 Rothmund-thomson syndrome MalaCards C2237041 Shox gene with short stature C3280616 Cranioectodermal dysplasia 4 MalaCards C0016199 Pain flank C1514837 Renal cell carcinoma associated with t(x;17)(p11.2;q25) UMLS C0000737 Abdomen pain C0278698 Childhood hepatoma, group iii UMLS C0085636 Light sensitivity C0339284 Polymorphous corneal dystrophy MalaCards|HPO C1963064 Anxiety adverse event C1864871 Chromosome 17q21.31 deletion syndrome MalaCards C1145670 Failure respiratory C1843633 Myopathy, distal, with early respiratory failure, autosomal dominant MalaCards C0850758 Pain pelvic C0302148 Blood clot HSDN C0030193 Sense of pain C0029899 Otosclerosis HSDN C0000727 Abdomen acute C0012644 Animal disease models HSDN C0003862 Pain joint C2350242 Osteoarthritis, spine HSDN C0032617 High urine output C0393571 Multiple system atrophy HSDN C0413252 Hypothermia due to exposure C0017178 Gastrointestinal diseases HSDN C1557397 Adverse event associated with pain C0342649 Vascular calcification HSDN C0026838 Spasticity muscle C2586211 Thrombosis of blood vessel HSDN C1384666 Decreased hearing C1548777 Specimen reject reason - hemolysis HSDN C0007758 Cerebellar ataxia C1420653 Tcn2 gene HPO C0042571 Vertigo subjective C0006663 Calcinosis HSDN C0022346 Yellow skin C0042487 Venous thrombosis HSDN C0080233 Dental loss C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards C0234146 Absent reflex C1832334 Charcot-marie-tooth disease, type 4d MalaCards|HPO C0023015 Language handicap C0600260 Lung diseases, obstructive HSDN C0085636 Light sensitivity C3888401 Albinism, oculocutaneous, type v MalaCards|UMLS C0700078 Deep tendon reflex decrease C1834304 Amyotrophy, hereditary neuralgic MalaCards|HPO C3829611 Nausea frequency C4085311 Depression - recess HSDN C0030794 Pelvis pain C3495422 Finding relating to sexuality and sexual activity HSDN C1579931 Depressed - symptom C1858496 Advanced sleep-phase syndrome, familial HPO C2237041 Shox gene with short stature C0015624 Fanconi syndrome HPO C3898969 Have been vomiting C0014547 Epilepsies, partial HSDN C1971624 Appetite absent C0013124 Behavior drinking HSDN C2237041 Shox gene with short stature C1853576 Diamond-blackfan anemia with microtia and cleft palate HPO C1504494 Tingling in extremities C0003467 Anxiety UMLS C0015230 Exanthem C0268663 Vit a defic.+ xeroderma UMLS C1963093 Dizziness adverse event C0041296 Tuberculosis HSDN C0424755 Fever symptoms C0008519 Ectopic tissue HSDN C0028738 Nystagmus C0034960 Refsum disease HPO C4084774 Have weight loss C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0036572 Convulsion C0032858 Powassan encephalitis MalaCards C0022346 Yellow skin C0023903 Liver neoplasms MalaCards C0042571 Vertigo subjective C1865323 Migraine, familial basilar HPO C0009806 Constipate C1858517 Spinal muscular atrophy with respiratory distress 1 HPO|UMLS C0426579 Anorexia symptom C0520779 Human ehrlichial infection, sennetsu type MalaCards C0557874 Global developmental delay C2750027 Growth hormone deficiency with pituitary anomalies MalaCards|HPO C1971624 Appetite absent C0040947 Trichostrongyloidiasis HSDN C4084727 Cough frequency C3495801 Granulomatosis with polyangiitis OrphaNet|HSDN|HPO|MalaCards C0011206 Delirium acute C1269683 Major depressive disorder HSDN C4084723 Constipation C3665349 Secondary hypothyroidism OrphaNet|MalaCards C4085222 Nausea C0085183 Neoplasms, second primary HSDN C0040822 D tremors C3542026 Peroxisome biogenesis disorder 5b MalaCards|UMLS C2024893 Cardiovascular surgery result: fatigue C0271815 Postpartum thyroiditis HSDN C0036572 Convulsion C0025293 Meningitis, listeria HSDN C0151686 Growth retardation C2673642 Combined oxidative phosphorylation deficiency 5 MalaCards|HPO C0003467 Angst C0268275 Tay-sachs disease, ab variant MalaCards C2984058 Have pain C0032780 Postmortem changes HSDN C4085549 Dizziness C0271355 Abducens nerve paralysis HSDN C2700617 Irritation - emotion C1420653 Tcn2 gene HPO C2911645 Weight loss adverse event C0042995 Vulvar neoplasms HSDN C2911647 Weight gain adverse event C0344479 Spinal cord myelodysplasia HSDN C0036572 Convulsion C3149814 Retinal dystrophy, early-onset, with pituitary dysfunction HPO C0271215 Blindness legal C1869114 Weill-marchesani syndrome, autosomal recessive HPO C4084802 Usual severity diarrhea C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0013404 Respiratory difficulty C0040156 Thyrotoxicosis HSDN C2237041 Shox gene with short stature C0410539 Craniodiaphyseal dysplasia OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0149514 Bronchitis acute HSDN C4084774 Have weight loss C0002871 Anemia HSDN C1963137 Hydrocephalus adverse event C3536727 Triploidy MalaCards C2984058 Have pain C0030528 Paratyphoid fever HSDN C0039070 Collapse fleeting C0340493 Paroxysmal familial ventricular fibrillation MalaCards C4085661 Usual severity nausea C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0521800 Central cyanosis C0152021 Congenital heart disease UMLS C0013604 Edematous C0001327 Laryngitis acute HSDN C0241137 Skin pallor C1861848 Paragangliomas 4 MalaCards C4084774 Have weight loss C0034063 Pulmonary edema HSDN C3463815 Feel fatigue C0036467 Scrofula MalaCards C4084723 Constipation C0242342 Sheehan syndrome MalaCards C0018784 Deafness sensorineural C2984572 Malaria pathway HSDN C0022107 Fussiness C0268581 Holocarboxylase synthetase deficiency OrphaNet|HPO|MalaCards C0007398 Catatonic C0041327 Tuberculosis, pulmonary HSDN C0018834 Brash C1836522 Schindler disease, type ii MalaCards C0015672 Decreased energy C0015397 Disorder of eye HSDN C0030193 Sense of pain C1299437 Angina recurrent status post coronary stent placement UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0016989 Galvanic skin response HSDN C0023530 Leukopenia C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0030193 Sense of pain C0018235 Aggrieved HSDN C0036396 Sciatica C0004153 Atherosclerosis HSDN C0000737 Abdomen pain C0027627 Neoplasm metastasis HSDN C4084766 Vomiting C0001144 Acne vulgaris HSDN C1527344 Dysphonia C0015458 Facial hemiatrophy HSDN C0344315 Mood depressed C2931205 Usher syndrome, type 1a MalaCards C4085317 Diarrhea frequency C0346407 Pancreatic polypeptide-oma MalaCards C0042025 Urinary incontinence stress C0040038 Thromboembolism HSDN C0030193 Sense of pain C0242172 Pelvic inflammatory disease HSDN C0042940 Disorder of voice C1263846 Attention deficit hyperactivity disorder HSDN C1384666 Decreased hearing C0007621 Neoplastic cell transformation HSDN C0728710 Pupil constriction observed C0078918 Albinism, oculocutaneous HSDN C0022346 Yellow skin C0233629 Thinking and speaking disturbances HSDN C0003910 Articulation disorder C0520679 Sleep apnea, obstructive HSDN C0040485 Wryneck C0027868 Neuromuscular diseases HSDN C1557397 Adverse event associated with pain C1704326 Role - roleclass HSDN C4084774 Have weight loss C0024636 Malocclusion HSDN C0151889 Reflexes tendon increased C1854568 Spastic paraplegia 14, autosomal recessive (disorder) MalaCards C4018871 Abnormality of the respiratory system C0031269 Peutz-jeghers syndrome MalaCards C0349588 Stature short C3150790 Chromosome 6q11-q14 deletion syndrome MalaCards C0013390 Cramps menstrual C0022658 Kidney diseases HSDN C4085317 Diarrhea frequency C0026552 Morphine dependence HSDN C2029884 Hearing loss by exam C0017653 Glomus tumor HSDN C0086565 Liver function abnormal C0748397 Reynolds syndrome MalaCards|HPO C4084723 Constipation C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0015469 Facial paralysis C0004161 Athletic injuries HSDN C0018524 Hallucinate C0023890 Liver cirrhosis HSDN C0036572 Convulsion C4015316 Epileptic encephalopathy, early infantile, 27 MalaCards|UMLS C0002965 Crescendo angina C0009240 Cognition HSDN C4084774 Have weight loss C0014511 Epithelial cyst HSDN C0012569 Double vision C0161398 Neuropathy optic traumatic HSDN C0015970 Fever unknown origin C0031085 Periodontal abscess HSDN C0009806 Constipate C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards|UMLS C0151825 Ostalgia C0279593 B-cell adult acute lymphoblastic leukemia UMLS C0848203 Male pelvic pain C0027765 Nervous system disorder HSDN C1549543 Administration method - pain C0025286 Meningioma HSDN C0151908 Dry skin C4225670 Anhidrosis, familial generalized, with abnormal or absent sweat glands UMLS C0015469 Facial paralysis C0262655 Recurrent urinary tract infection HSDN C0917801 Sleep disorder insomnia C0038454 Cerebrovascular accident UMLS C0024032 Birth weight subnormal C3281289 Trichohepatoenteric syndrome 2 MalaCards C1963071 Back pain adverse event C1261473 Sarcoma HSDN C0085636 Light sensitivity C1846529 Cone-rod dystrophy 10 MalaCards|HPO C0700078 Deep tendon reflex decrease C3151753 Combined oxidative phosphorylation deficiency 6 MalaCards C0000737 Abdomen pain C0042063 Urogenital abnormalities HSDN C0557874 Global developmental delay C0339527 Leber congenital amaurosis MalaCards|HPO C0151315 Neck rigid C0750929 Arnold-chiari malformation, type i MalaCards C0035078 Failure kidney C3280216 Hnfj3 MalaCards C0040034 Thrombocytopenia C2678311 Thrombocytopenia 3 HPO C4018871 Abnormality of the respiratory system C0398621 Hypoplasminogenemia MalaCards|HPO C0013911 Emaciate C1962963 Osteoporosis adverse event HSDN C2911645 Weight loss adverse event C0020598 Hypocalcemia HSDN C0015970 Fever unknown origin C0002797 Bovine anaplasmosis HSDN C0013390 Cramps menstrual C0037072 Diseases sigmoid HSDN C0030200 Intractable pain C0014544 Epilepsy HSDN C0795701 Neck spasm C0741413 Back spasm upper back UMLS C1963252 Tremor adverse event C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C0427055 Face weakness C3808739 Myasthenic syndrome, congenital, 8 UMLS C1319588 On examination - referable retinopathy C0035309 Retinal diseases UMLS C0020673 Hypothermia (central) (local) C0031154 Peritonitis HSDN C0033790 Pseudobulbar palsy C0085541 Epilepsy, frontal lobe HSDN C0020580 Decreased sensation C0013364 Dysautonomia, familial HSDN C1963063 Anorexia adverse event C0040053 Thrombosis HSDN C2911645 Weight loss adverse event C0000771 Abnormalities, drug induced HSDN C0030193 Sense of pain C0039980 Chest injury HSDN C3829611 Nausea frequency C0035412 Rhabdomyosarcoma HSDN C0018681 Headache, cephalalgia C0011586 Three dimensional vision HSDN C0522224 Palsied C0026266 Mitral valve insufficiency HSDN C4084784 Diarrhea C2749484 Neuroblastoma, susceptibility to HPO C4084726 Distress cough C0042373 Vascular diseases HSDN C3539889 Pelvic pain increasing in severity C0796561 Melanoma vaccines HSDN C0001707 Aerophagia C1720922 Respiratory aspiration HSDN C4085317 Diarrhea frequency C4084971 Trachoma HSDN C0080233 Dental loss C0398621 Hypoplasminogenemia MalaCards C1549543 Administration method - pain C0751795 Head injury penetrating HSDN C0518090 Frequency of pain question C0340464 Heartbeats ectopic HSDN C2315100 Pediatric failure to thrive C0043208 Wolman disease HPO C4084726 Distress cough C0039685 Tetralogy of fallot HSDN C0242936 Center pain C0281865 Hip injury HSDN C1579931 Depressed - symptom C1847987 Huntington disease-like 2 MalaCards|HPO C0041105 Jaw spasm C1332140 Acrofacial dysostosis MalaCards C4084775 Usual severity weight loss C0024810 Marijuana smoking HSDN C0349588 Stature short C1275081 Cardio-facio-cutaneous syndrome OrphaNet|HPO C0043094 Weight gain C0041234 Chagas disease HSDN C2029884 Hearing loss by exam C0524801 Retinal neoplasms HSDN C0013421 Dystonia C0023374 Lesch-nyhan syndrome MalaCards|HPO C0004134 Dyssynergia C0021368 Inflammation HSDN C3641755 Have constipation C0001973 Alcoholic intoxication, chronic HSDN C0036572 Convulsion C0422859 Seizure, partial, dysmnesic UMLS C1069915 Vertigo C1956346 Coronary artery disease HSDN C0009421 Comatose C1864952 Hyperinsulinemic hypoglycemia, familial, 5 MalaCards C4084775 Usual severity weight loss C1546602 Specimen source codes - diverticulum HSDN C0497406 Over weight C0030305 Pancreatitis HSDN C0038002 Spleen enlargement C0391826 Lhermitte-duclos disease MalaCards C1963065 Apnea adverse event C0042830 Perception visual HSDN C0424755 Fever symptoms C0018818 Ventricular septal defects HSDN C0003469 Anxiety disorder C2676739 Chromosome 2q32-q33 deletion syndrome MalaCards|HPO C0162835 Hypopigmentation C3495588 Acrocephalopolydactylous dysplasia MalaCards C0026821 Cramp C1862941 Amyotrophic lateral sclerosis, sporadic HPO C0751534 Syncopal episode C4225199 Muscular dystrophy, limb-girdle, type 2x UMLS C0005745 Blepharoptosis C1864649 Myasthenia, limb-girdle, with tubular aggregates HPO C1279888 Proteinuria of undiagnosed cause C0024535 Malaria, falciparum HSDN C0018681 Headache, cephalalgia C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C2911647 Weight gain adverse event C0001314 Acute disease HSDN C4084784 Diarrhea C1857449 Cutaneous photosensitivity and colitis, lethal MalaCards C0557874 Global developmental delay C1832585 Cerebellar ataxia, cayman type HPO C0020505 Excessive eating C3809844 Chromosome 22q13 duplication syndrome MalaCards C0243026 Generalized infection C0038325 Stevens-johnson syndrome HPO C3829611 Nausea frequency C0006145 Breast diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0334299 Carcinoid tumor no icd-o subtype HSDN C0014591 Bleeding nose C1853278 Bleeding disorder due to p2ry12 defect MalaCards|HPO C4085549 Dizziness C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0917816 Deficiency mental C3809160 Shaheen syndrome MalaCards C0000737 Abdomen pain C2030691 Gallbladder hepatoid adenocarcinoma UMLS C0005745 Blepharoptosis C1275081 Cardio-facio-cutaneous syndrome OrphaNet|HPO C0848203 Male pelvic pain C0001261 Actinomycosis HSDN C4084724 Usual severity constipation C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C0015970 Fever unknown origin C0206369 Splenosis HSDN C0240715 Perineal lump C3696981 Paratesticular malignant neoplasm UMLS C4084767 Bothered by vomiting C0003838 Arterial occlusive diseases HSDN C2237041 Shox gene with short stature C1850102 Palant cleft palate syndrome MalaCards C2242996 Tingling C0080179 Vertebra fracture HSDN C0497406 Over weight C0030286 Pancreatic diseases HSDN C1963281 Vomiting adverse event C0005940 Bone diseases HSDN C0015469 Facial paralysis C0270726 Alexander disease OrphaNet|MalaCards C0023015 Language handicap C1269683 Major depressive disorder HSDN C2029884 Hearing loss by exam C1999266 Depression adverse event HSDN C1000483 Genus anemia C0024534 Malaria, cerebral MalaCards C1384666 Decreased hearing C2931426 Orofaciodigital syndrome type1 HPO C0015672 Decreased energy C1963067 Atrial fibrillation adverse event HSDN C1549543 Administration method - pain C0040124 Thyroglossal duct cyst HSDN C2984058 Have pain C3542413 Cdisc adas-cog - comprehension HSDN C0151786 Weakness muscle C3150730 Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency HPO C3463815 Feel fatigue C0524851 Neurodegenerative disorders HSDN C0014534 Epididymitis unspecified C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C0033790 Pseudobulbar palsy C0238052 Xanthomatosis, cerebrotendinous MalaCards|HPO C0030486 Extremity paralysis, lower C4050613 Anxiety scale (basc-2) HSDN C0004941 Behavioral symptoms C1857052 Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia OrphaNet|MalaCards C0476250 Head neck mass C0343643 Facial wart UMLS C0917816 Deficiency mental C3810282 Chromosome 5q12 deletion syndrome MalaCards C4085548 Usual severity dizziness C0005974 Bone resorption HSDN C1999266 Depression adverse event C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0344428 Ventricular tachycardia by ecg finding C1843896 Arrhythmogenic right ventricular dysplasia, familial, 8 HPO C0042798 Vision dim C1834079 Nystagmus 2, congenital, autosomal dominant (disorder) MalaCards C0042571 Vertigo subjective C1963119 Stomach ulcer adverse event HSDN C1279888 Proteinuria of undiagnosed cause C0028738 Nystagmus HSDN C4084774 Have weight loss C0015456 Facial dermatoses HSDN C2984058 Have pain C0038013 Ankylosing spondylitis DiseaseOntology|MalaCards C4084784 Diarrhea C0026865 Mushroom poisoning HSDN C0413252 Hypothermia due to exposure C0795623 Hepatitis a vaccine, inactivated HSDN C0031315 Phantom limb pain C0428953 Ecg infarction myocardial HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C1843738 Long qt syndrome 1, acquired, susceptibility to HPO C0018784 Deafness sensorineural C0020502 Hyperparathyroidism HSDN C0150055 Pain chronic C1384606 Dyspareunia HSDN C0041657 Consciousness loss C0149931 Migraine disorders HSDN C0686347 Dyskinesia tardive C3714760 Drug-induced tardive dyskinesia MalaCards C4084769 Vomiting frequency C0005937 Bone cysts HSDN C4084767 Bothered by vomiting C0997768 Glaucoma HSDN C1549543 Administration method - pain C0003962 Ascites HSDN C3541349 Syncope C0860603 Anxiety symptoms HSDN C0004134 Dyssynergia C0003811 Cardiac arrhythmia HSDN C1557397 Adverse event associated with pain C0600518 Choroidal neovascularization HSDN C0751495 Seizure focal C3279743 Spastic paraplegia 52, autosomal recessive MalaCards C0242936 Center pain C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C1000483 Genus anemia C1858592 Carney triad MalaCards C0041657 Consciousness loss C0021400 Influenza HSDN C4085210 Usual severity pain C0031154 Peritonitis HSDN C0424755 Fever symptoms C0037275 Skin diseases, vesiculobullous HSDN C4084767 Bothered by vomiting C0028433 Nose neoplasms HSDN C0037763 Spasm C0027868 Neuromuscular diseases HSDN C0002962 Angina C1550672 Specimen type - ulcer HSDN C3641756 Have diarrhea C0009376 Colonic polyps HSDN C0013395 Indigestion C3814778 Hemolytic index HSDN C0149793 Transient monocular blindness C0042376 Vascular headaches HSDN C0271215 Blindness legal C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0042928 Paralysis vocal cord C0005604 Trauma birth HSDN C1090821 Sepsis C0085110 Severe combined immunodeficiency OrphaNet|MalaCards C4084767 Bothered by vomiting C0033054 Prenatal exposure delayed effects HSDN C0086565 Liver function abnormal C1261128 Progeria-like syndrome MalaCards C0850758 Pain pelvic C0017181 Gastrointestinal hemorrhage HSDN C2096293 Ent surgical result ear vertigo C0033923 Psychomotor function HSDN C4020887 Photodysphoria C0221036 Acrodermatitis enteropathica OrphaNet|HPO C3463815 Feel fatigue C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C1963091 Diarrhea adverse event C0010346 Crohn disease MalaCards C0034933 Abnormal reflexes C0206157 Myopathies, nemaline HSDN C1000483 Genus anemia C3809522 Infantile liver failure syndrome 1 MalaCards C0013604 Edematous C1856305 Gsd iv, neuromuscular form, childhood MalaCards|HPO C1557397 Adverse event associated with pain C0006107 Concussion HSDN C3274924 Have been coughing C1550639 Specimen type - fistula HSDN C0033377 Caudal displacement C3810212 Joubert syndrome 21 MalaCards C0028738 Nystagmus C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C3898969 Have been vomiting C0032851 Disease poultry HSDN C1971624 Appetite absent C1963067 Atrial fibrillation adverse event HSDN C0332563 Papulae C0024137 Lupus erythematosus, cutaneous OrphaNet C0013404 Respiratory difficulty C0020192 Hyaline membrane disease MalaCards|HSDN C0039070 Collapse fleeting C0017160 Gastroenteritis HSDN C0013421 Dystonia C1956346 Coronary artery disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0221021 Microangiopathic hemolytic anemia MalaCards C3541349 Syncope C4049994 Insulin resistance measurement HSDN C0853945 Oral mucosa blister C1864826 Epidermolysis bullosa, lethal acantholytic OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0024694 Mandibular neoplasms HSDN C0037317 Sleep disturbance C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C1549543 Administration method - pain C0033839 Pseudorabies HSDN C0003862 Pain joint C0034734 Raynaud disease HSDN C0003862 Pain joint C1832998 Epiphyseal dysplasia, multiple, 3 MalaCards C0497247 Blood pressure elevation C4054549 Medullary cystic kidney disease type i MalaCards C0013404 Respiratory difficulty C0034084 Pulmonary infundib.stenosis HSDN C1145670 Failure respiratory C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C0015799 Feminisation C0919267 Ovarian neoplasm HSDN C0000727 Abdomen acute C0009241 Cognition disorders HSDN C3146279 Coma C0038358 Gastric ulcer HSDN C0009398 Color vision defects C2674009 Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma MalaCards|HPO C0009806 Constipate C3897537 Stage iia rectal cancer UMLS C0015230 Exanthem C0571418 Ampicillin allergy UMLS C0030554 Abnormal sensation C0085084 Motor neuron disease HSDN C3463815 Feel fatigue C0002884 Hypochromic anemia HSDN C4084784 Diarrhea C1522137 Hypertriglyceridemia result HSDN C0023014 Developmental disorder language C0242952 Behavior infants HSDN C0686770 Leser-trelat sign C0030472 Paraneoplastic syndromes UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0019021 Hemoglobin c disease HSDN C0038990 Sweats C0031511 Pheochromocytoma MalaCards|HPO C4085317 Diarrhea frequency C0041466 Typhoid fever DiseaseOntology|HSDN|MalaCards C1963281 Vomiting adverse event C0032131 Plasmacytoma HSDN C4085661 Usual severity nausea C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C2911645 Weight loss adverse event C0266836 Infantile colic HSDN C1963091 Diarrhea adverse event C0750394 Wbc low HSDN C0850758 Pain pelvic C1546602 Specimen source codes - diverticulum HSDN C4084784 Diarrhea C2931242 Familial waldmann's disease MalaCards C4084802 Usual severity diarrhea C1257806 Chromosomal instability MalaCards C0009676 Confusion state C0019151 Hepatic encephalopathy HSDN C1963071 Back pain adverse event C0006434 Burn injury HSDN C4084788 Have dizziness C0033871 Psychiatric status rating scales HSDN C4084774 Have weight loss C0032787 Postoperative complications HSDN C4084784 Diarrhea C0020732 Iatrogenic disease HSDN C4084773 Bothered by weight gain C0018939 Hematological disease HSDN C0018784 Deafness sensorineural C2609414 Acute kidney injury HSDN C2911645 Weight loss adverse event C0037361 Olfactory sense HSDN C0011206 Delirium acute C0042830 Perception visual HSDN C2237041 Shox gene with short stature C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C0042963 Symptoms vomiting C2586211 Thrombosis of blood vessel HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0004096 Asthma HSDN C4085317 Diarrhea frequency C0014556 Epilepsy, temporal lobe HSDN C4085211 Pain distress question C0008065 Childhood behavior HSDN C4085222 Nausea C0032285 Pneumonia HSDN C0020672 Body temperature decreased C0376618 Endotoxemia HSDN C0028738 Nystagmus C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C3539896 Pelvic pain occurs with urination C0302148 Blood clot HSDN C4084775 Usual severity weight loss C0086768 Pancreatic cholera OrphaNet|MalaCards C0033774 Skin pruritus C0043251 Wounds and injuries HSDN C4084773 Bothered by weight gain C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C0234979 Dysdiadochokinesia C0007760 Cerebellar diseases UMLS C2911647 Weight gain adverse event C2984330 Chagas disease pathway HSDN C0022346 Yellow skin C0546323 Inferior vena cava membranous obstruction MalaCards C1069915 Vertigo C0796561 Melanoma vaccines HSDN C1963184 Nystagmus adverse event C2750747 Night blindness, congenital stationary, type 1c HPO C0022346 Yellow skin C0268307 Conjugated hyperbilirubinemia MalaCards C4084727 Cough frequency C0004576 Babesiosis OrphaNet|MalaCards C2315100 Pediatric failure to thrive C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C1963137 Hydrocephalus adverse event C1839909 Corpus callosum, partial agenesis of, x-linked HPO C2024893 Cardiovascular surgery result: fatigue C0014461 Granuloma eosinophilic MalaCards C4085548 Usual severity dizziness C0027902 Neuropsychological diagnosis HSDN C4084773 Bothered by weight gain C0026267 Mitral valve prolapse syndrome HSDN C0011175 Deficient fluid volume C0085548 Autosomal recessive polycystic kidney disease HPO C0002622 Amnesias C3811918 Grn-related frontotemporal dementia HSDN C0000737 Abdomen pain C1336861 Undifferentiated pancreatic carcinoma UMLS C0274369 Pain due to any device, implant or graft C2106870 Pain due to renal dialysis device, implant, or graft UMLS C0040485 Wryneck C1138434 Disease, x-linked genetic HSDN C0009763 Conjunctiva inflammation C2718078 Deficiency of uroporphyrinogen iii synthase MalaCards|HPO C0011991 Loose stools C0015695 Fatty liver HSDN C1962972 Proteinuria adverse event C0023976 Long qt syndrome HSDN C2984058 Have pain C0025299 Meningocele HSDN C0917816 Deficiency mental C1848070 Lissencephaly and agenesis of corpus callosum HPO C1963091 Diarrhea adverse event C2674051 Inflammatory bowel disease 11 MalaCards C0019521 Hiccoughs C0279626 Squamous cell carcinoma of esophagus MalaCards C1557397 Adverse event associated with pain C0018571 Hand injury HSDN C0239376 Lower extremity pain C0340708 Lower extremity deep venous thrombosis UMLS C0332563 Papulae C0545044 Acrokeratoelastoidosis of costa OrphaNet|MalaCards C0221166 Paraparesis C0027888 Hereditary motor and sensory neuropathies HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1963235 Sick sinus syndrome adverse event HSDN C2984057 Have nausea C0023743 Linitis plastica HSDN C2911647 Weight gain adverse event C0679360 Foodborne disease HSDN C0019825 Voice hoarseness C0263628 Tumoral calcinosis MalaCards C1963071 Back pain adverse event C0043251 Wounds and injuries HSDN C0027066 Myoclonic jerking C0597109 Nurse's role HSDN C0231528 Muscle pain generalized C0948264 Neuroborreliosis MalaCards C0018777 Deafness, conductive C1956390 Cranial arteritis MalaCards C4084784 Diarrhea C0342793 Malonic aciduria MalaCards|HPO C3541349 Syncope C0009240 Cognition HSDN C0460137 Push down or depress C1568248 Usher syndrome, type iii MalaCards|HPO C0011991 Loose stools C0040809 Patient refusal of treatment HSDN C4084802 Usual severity diarrhea C0006105 Brain abscess HSDN C2911647 Weight gain adverse event C0001969 Alcoholic intoxication HSDN C1384666 Decreased hearing C0016065 Polyostotic fibrous dysplasia HPO C0042928 Paralysis vocal cord C0040053 Thrombosis HSDN C1860844 Sparse, thin hair C0432267 Tricho thiodystrophy disorder MalaCards C0003862 Pain joint C0023804 Lipomatosis, multiple symmetrical OrphaNet|HPO|MalaCards C0030193 Sense of pain C1723764 Chronic prostatitis with chronic pelvic pain syndrome UMLS C0026884 Muteness C3539760 Mok wt allele HSDN C0007758 Cerebellar ataxia C1837454 Spinocerebellar ataxia 8 MalaCards C0012833 Dizzy C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0854723 Retinal dystrophies HSDN C3274924 Have been coughing C0027643 Neoplasm recurrence, local HSDN C3463815 Feel fatigue C0034072 Cor pulmonale HSDN C0016204 Fart C0020701 Somatization disorder HSDN C0242936 Center pain C0752155 Central nervous system vascular malformations HSDN C0012833 Dizzy C0016658 Fracture bone HSDN C2911645 Weight loss adverse event C0038358 Gastric ulcer HSDN C0010200 Cough symptom C0008073 Developmental disabilities HSDN C0033774 Skin pruritus C0017689 Glucagonoma OrphaNet|MalaCards C0040264 Ear ringing sound C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4084802 Usual severity diarrhea C0023223 Leg ulcer HSDN C0518090 Frequency of pain question C0162566 Porphyria cutanea tarda HSDN C2315100 Pediatric failure to thrive C0028860 Oculocerebrorenal syndrome OrphaNet|HSDN|HPO C1963177 Muscle pain adverse event C1306220 Fort bragg fever MalaCards C0030232 Color loss C1838103 Mitochondrial myopathy and sideroblastic anemia HPO C0016199 Pain flank C0007095 Carcinoid tumor HSDN C1963170 Hypothermia adverse event C0021051 Immunologic deficiency syndromes HSDN C0413252 Hypothermia due to exposure C1269683 Major depressive disorder HSDN C0028738 Nystagmus C1862263 Bpes without ovarian failure HPO C0700590 Diaphoresis excessive C0271889 Diencephalic syndrome of infancy OrphaNet|MalaCards C1527344 Dysphonia C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0042963 Symptoms vomiting C4049994 Insulin resistance measurement HSDN C0020672 Body temperature decreased C0021603 Sleep initiation and maintenance disorders HSDN C4084802 Usual severity diarrhea C0018794 Heart block HSDN C0019825 Voice hoarseness C0023075 Laryngostenosis HSDN C1963252 Tremor adverse event C0015745 Ingestive behavior HSDN C4084897 Sleep disturbance subordinate domain C1868570 Char syndrome MalaCards|HPO C0013911 Emaciate C0162651 Gastric outlet obstruction HSDN C0497406 Over weight C0026613 Motor skills disorders HSDN C1856661 Cornea cloudy C2931585 Gaucher-like disease MalaCards C2024893 Cardiovascular surgery result: fatigue C0026266 Mitral valve insufficiency HSDN C4085211 Pain distress question C0235833 Congenital diaphragmatic hernia HSDN C0155002 Vision loss acute C1263864 Blindness and/or vision impairment level UMLS C0751495 Seizure focal C0270847 Benign focal epilepsy, childhood UMLS C0036659 Sensation disorder C0001818 Agoraphobia HSDN C0270948 Neurogenic muscular atrophy C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C1963249 Tinnitus adverse event C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0030486 Extremity paralysis, lower C0020179 Huntington disease HSDN C4084725 Usual severity cough C0524799 Hyperlucent lung HSDN C0036572 Convulsion C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards|HPO|UMLS C0241137 Skin pallor C2751986 Retinitis pigmentosa 42 MalaCards|HPO C1549543 Administration method - pain C0018378 Guillain-barre syndrome HSDN C3146279 Coma C0860603 Anxiety symptoms HSDN C4049644 Depression C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C0234132 Pyramidal sign C1860808 Triosephosphate isomerase deficiency UMLS C0009676 Confusion state C1963064 Anxiety adverse event HSDN C2911645 Weight loss adverse event C0017563 Gingival diseases HSDN C0349588 Stature short C0268312 Progressive intrahepatic cholestasis (disorder) OrphaNet C0040264 Ear ringing sound C1847839 Episodic ataxia, type 3 MalaCards C0004604 Pain back C0238909 Cat scratch MalaCards C4085317 Diarrhea frequency C0018939 Hematological disease HSDN C2024893 Cardiovascular surgery result: fatigue C0008354 Cholera HSDN C0031256 Petechia C0005956 Bone marrow diseases MalaCards C2024878 Cardiovascular surgery result: dyspnea C0034345 Pyruvate dehydrogenase complex deficiency disease MalaCards C0030552 Paralysis partial C0008626 Congenital chromosomal disease HSDN C0577567 Mass of urogenital structure C0178251 Malig neop genitourinary nos UMLS C0013604 Edematous C0029291 Fever, parrot HSDN C1384666 Decreased hearing C0019699 Hiv seropositivity HSDN C1963071 Back pain adverse event C0035222 Respiratory distress syndrome, adult HSDN C0018772 Deafness C0265421 Warkany syndrome MalaCards C0037771 Paraparesis spastic C0339143 Thyroid associated opthalmopathies HSDN C3815497 Cough C0023470 Myeloid leukemia HSDN C0022107 Fussiness C0020074 Hsan type iv OrphaNet|HPO|MalaCards C3829611 Nausea frequency C0021818 Intervertebral disk displacement HSDN C0022346 Yellow skin C1963119 Stomach ulcer adverse event HSDN C0030193 Sense of pain C0206692 Carcinoma, lobular HSDN C2919142 Short stature adverse event C0796004 Kabuki make-up syndrome OrphaNet|HPO|MalaCards C0231712 Gait waddling C1834690 Spinal muscular atrophy, childhood, proximal, autosomal dominant HPO|UMLS C0030193 Sense of pain C0035613 Rift valley fever HSDN C0002962 Angina C0034067 Pulmonary emphysema HSDN C0012833 Dizzy C0041755 Adverse reaction to drug HSDN C0151786 Weakness muscle C0028326 Noonan syndrome OrphaNet|HPO|MalaCards C0557874 Global developmental delay C1869122 Ehlers-danlos syndrome, progeroid form OrphaNet|HPO|MalaCards C4085211 Pain distress question C0017536 Giardiasis HSDN C3887784 Decreased urine output C0162739 Hellp syndrome HSDN C0011175 Deficient fluid volume C3543867 Collodion fetus MalaCards C4084769 Vomiting frequency C0036341 Schizophrenia HSDN C4042891 Sleep wake disorders C0017636 Glioblastoma HSDN C0332573 Macula C2936881 Eosinophilic synovitis MalaCards C4084723 Constipation C0162671 Melas syndrome MalaCards|HPO C0000737 Abdomen pain C0016658 Fracture bone HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0017181 Gastrointestinal hemorrhage HSDN C0027497 Queasy C0043019 Lateral medullary syndrome HSDN C4084768 Usual severity vomiting C0034530 Injury radiation HSDN C0237326 Defecation pain C0585274 Periodic syndrome OrphaNet|HPO C0000737 Abdomen pain C0017205 Gaucher disease OrphaNet|MalaCards C0009806 Constipate C0023176 Lead poisoning MalaCards|HSDN C0427055 Face weakness C0238288 Muscular dystrophy, facioscapulohumeral MalaCards|HPO C0016927 Gag reflex C0023051 Laryngeal diseases HSDN C0011168 Disorder deglutition C1848814 Thymoma, familial MalaCards C0036572 Convulsion C3553637 Hyperphosphatasia with mental retardation syndrome 2 MalaCards C1963252 Tremor adverse event C0011853 Diabetes mellitus, experimental HSDN C4084776 Weight loss C2936350 Plaque, atherosclerotic HSDN C4084802 Usual severity diarrhea C0015745 Ingestive behavior HSDN C0030552 Paralysis partial C0008728 Churg-strauss syndrome HSDN C0042025 Urinary incontinence stress C0002989 Epithelioid hemangioma of skin HSDN C0007758 Cerebellar ataxia C3150801 Combined oxidative phosphorylation deficiency 7 MalaCards|HPO C4084784 Diarrhea C0342443 Adrenal cushing's syndrome HSDN C0010200 Cough symptom C3714509 Nutrition disorders HSDN C4084725 Usual severity cough C1761609 Aspiration pneumonitis MalaCards C0040822 D tremors C1839564 Jensen syndrome MalaCards C4084773 Bothered by weight gain C0027868 Neuromuscular diseases HSDN C0848203 Male pelvic pain C0243001 Abdominal abscess HSDN C0018777 Deafness, conductive C0030421 Paraganglioma HSDN|HPO C0036572 Convulsion C3553597 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome MalaCards C0009676 Confusion state C0007761 Myoclonic cerebellar dyssynergia HSDN C0424755 Fever symptoms C0025007 Measles DiseaseOntology|MalaCards C0009792 Consciousness disorder C0025290 Aseptic meningitis HSDN C1549543 Administration method - pain C0043395 Yellow fever HSDN C1963063 Anorexia adverse event C0038436 Post-traumatic stress disorder HSDN C0042963 Symptoms vomiting C1621920 Intermediate maple syrup urine disease HPO C1384666 Decreased hearing C0038941 Incisional infection HSDN C4085211 Pain distress question C0039585 Androgen-insensitivity syndrome HSDN C3898969 Have been vomiting C0037361 Olfactory sense HSDN C4085211 Pain distress question C0041974 Urethral stricture HSDN C0018777 Deafness, conductive C0206731 Angiofibroma HSDN C0036572 Convulsion C0008479 Chondrosarcoma HSDN C0011991 Loose stools C0036329 Schistosomiasis japonica DiseaseOntology C1549543 Administration method - pain C0869332 Of water deprivation HSDN C0018681 Headache, cephalalgia C0010709 Cyst HSDN C2984058 Have pain C0085693 Acute appendicitis nos (disorder) MalaCards C0023380 Lethargy C1829703 Carnitine palmitoyl transferase 1a deficiency OrphaNet|HPO|UMLS C0162285 Edema eyelid C0009774 Conjunctivitis viral MalaCards C0557874 Global developmental delay C2676739 Chromosome 2q32-q33 deletion syndrome OrphaNet|HPO|MalaCards C0023012 Delay language C0024408 Machado-joseph disease OrphaNet|MalaCards C0009806 Constipate C0012644 Animal disease models HSDN C4085211 Pain distress question C0024537 Malaria, vivax HSDN C3665492 Pigmentations C0151779 Cutaneous melanoma MalaCards C0019079 Bloody sputum C1265997 Large cell carcinoma with rhabdoid phenotype UMLS C0700078 Deep tendon reflex decrease C4015029 Charcot-marie-tooth disease, recessive intermediate d MalaCards C4085211 Pain distress question C0037889 Hereditary spherocytosis HSDN C2142181 Left knee pain C0810055 Other non-traumatic joint disorders UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0030636 Pasteurella infection HSDN C4084767 Bothered by vomiting C0238386 Cronkhite-canada disease MalaCards C0030552 Paralysis partial C0025299 Meningocele HSDN C0026838 Spasticity muscle C2931857 Double cortex MalaCards C4084768 Usual severity vomiting C0035436 Rheumatic fever HSDN C0036572 Convulsion C3536563 Atypical absence seizure, non-intractable UMLS C1961131 Cough adverse event C0001175 Acquired immunodeficiency syndrome HSDN C0004134 Dyssynergia C0032227 Pleural effusion disorder HSDN C4085211 Pain distress question C0005689 Bladder exstrophy HSDN C0557874 Global developmental delay C3151461 Lis4 MalaCards|HPO C0344315 Mood depressed C1851945 Dystonia 1, torsion, autosomal dominant HPO C4050613 Anxiety C0342442 Acth-dependent cushing's syndrome OrphaNet C1549543 Administration method - pain C0002448 Ameloblastoma HSDN C0012833 Dizzy C1963119 Stomach ulcer adverse event HSDN C0151786 Weakness muscle C0039263 Takayasu arteritis OrphaNet|HPO|MalaCards C1527344 Dysphonia C1866552 Paragangliomas 2 (disorder) MalaCards C1963077 Bone pain adverse event C0022739 Klippel-trenaunay-weber syndrome MalaCards C0030193 Sense of pain C0027438 Nasopharynx HSDN C1549543 Administration method - pain C0005424 Biliary tract diseases HSDN C0039070 Collapse fleeting C1334698 Meningothelial cell neoplasm MalaCards C2203646 Jaundice C0032964 Pregnancy complications, hematologic HSDN C0037763 Spasm C0314657 Genetic predisposition HSDN C0917816 Deficiency mental C3150876 Congenital disorder of glycosylation, type iii MalaCards|HPO C0010200 Cough symptom C0032229 Pleural neoplasms HSDN C0042963 Symptoms vomiting C0018809 Heart neoplasm HSDN C0151786 Weakness muscle C0751038 Cockayne syndrome, type ii HPO C0242936 Center pain C0004626 Pneumonia, bacterial HSDN C0003862 Pain joint C0023903 Liver neoplasms HSDN C1384666 Decreased hearing C0238163 Hereditary hyperphosphatasia MalaCards C0036572 Convulsion C1868598 Parietal foramina HPO|UMLS C0425791 Breast skin orange peel texture C0853972 Inflammatory carcinoma of breast stage iv UMLS C0151825 Ostalgia C0011989 Camurati-engelmann syndrome OrphaNet|HPO|MalaCards C0020672 Body temperature decreased C0026946 Mycoses HSDN C0010200 Cough symptom C0037120 Pneumonia, nitrogen dioxide HSDN C0518090 Frequency of pain question C0019069 Hemophilia a HSDN C0022346 Yellow skin C1332251 Ampulla of vater squamous cell carcinoma UMLS C2984058 Have pain C0752140 Intracranial embolism HSDN C0232286 Pain precordial C3203733 Precordial catch UMLS C4042891 Sleep wake disorders C0270327 Bedwetting HSDN C0004941 Behavioral symptoms C0162635 Angelman syndrome OrphaNet|MalaCards C0007758 Cerebellar ataxia C0025521 Inborn errors of metabolism HSDN C0518090 Frequency of pain question C0043324 Juvenile xanthogranuloma HSDN C3641755 Have constipation C0018939 Hematological disease HSDN C0727671 Red cross toothache drops C0038368 Stomatognathic diseases HSDN C1279888 Proteinuria of undiagnosed cause C1623041 Breast-fed HSDN C0030193 Sense of pain C0007789 Cerebral palsy HSDN C4084727 Cough frequency C0013473 Eating disorders HSDN C0241137 Skin pallor C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0022346 Yellow skin C1335256 Pretext stage 2 hepatoblastoma UMLS C2237041 Shox gene with short stature C1864851 Pigmented nodular adrenocortical disease, primary, 2 MalaCards C0424755 Fever symptoms C0003850 Arteriosclerosis HSDN C1963281 Vomiting adverse event C0242216 Biliary calculi HSDN C4084774 Have weight loss C1836327 Rhabdoid tumor predisposition syndrome 1 (disorder) MalaCards C4084769 Vomiting frequency C0043065 Water electrolyte imbalance HSDN C0270948 Neurogenic muscular atrophy C1527383 Morphea MalaCards C2237041 Shox gene with short stature C3805879 Precocious puberty, central, 1 MalaCards C0004134 Dyssynergia C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C1557397 Adverse event associated with pain C0035258 Restless legs syndrome HSDN C0033074 Presbycusis C0036341 Schizophrenia HSDN C0857305 Thrombocytopenia purpura C3541306 Plasmodium measurement HSDN C0037763 Spasm C0037937 Spine injury HSDN C0009460 Communication impairment C1546847 Entity name part type - family HSDN C0011206 Delirium acute C0031117 Peripheral neuropathy HSDN C0007859 Pain neck C0000833 Abscess HSDN C0008031 Pain chest C0239981 Hypoalbuminemia UMLS C2919424 Mass of uterine adnexa C0269178 Broad ligament; cyst UMLS C1963281 Vomiting adverse event C0041952 Uerterolithiasis HSDN C1962972 Proteinuria adverse event C0004114 Astrocytoma HSDN C3146279 Coma C1556682 Adverse event associated with infection HSDN C0027497 Queasy C0302497 Retrobulbar haemorrhage HSDN C3898969 Have been vomiting C0023176 Lead poisoning MalaCards C0007758 Cerebellar ataxia C1862099 Brachydactyly-nystagmus-cerebellar ataxia MalaCards C2032396 Pelvic pain on the right C0233894 Femininity HSDN C1279888 Proteinuria of undiagnosed cause C0878544 Cardiomyopathies HSDN C0086437 Joint hypermobility C3151211 Osteogenesis imperfecta, type x MalaCards|HPO C0023380 Lethargy C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C4085661 Usual severity nausea C0033873 Psychiatry HSDN C4084774 Have weight loss C0016470 Food allergy HSDN C0004134 Dyssynergia C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO|UMLS C0017181 Gastrointestinal bleed C0272317 Hereditary factor ii deficiency disease HPO C0473384 Edema or excessive weight gain in pregnancy without mention of hypertension, delivered with mention of postpartum complication C0341960 Edema pregnancy UMLS C0262384 Chest pain atypical C0003467 Anxiety UMLS C2029884 Hearing loss by exam C0041296 Tuberculosis HSDN C0476273 Distress respiratory C1853576 Diamond-blackfan anemia with microtia and cleft palate HPO C3539891 Pelvic pain to the rear C0242350 Erectile dysfunction HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0015579 Family characteristics HSDN C0027497 Queasy C0206245 Amyloid neuropathies, familial HSDN C0424755 Fever symptoms C0206604 Arterivirus infections HSDN C2984058 Have pain C0006110 Brain death HSDN C0042798 Vision dim C1857821 Leber congenital amaurosis 10 (disorder) MalaCards|HPO C3463815 Feel fatigue C0022972 Lambert-eaton myasthenic syndrome HSDN C0151686 Growth retardation C0029396 Heterotopic ossification MalaCards C0040034 Thrombocytopenia C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C4084788 Have dizziness C0029118 Opportunistic infections HSDN C4084727 Cough frequency C0038160 Staphylococcal infections HSDN C0018681 Headache, cephalalgia C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0030554 Abnormal sensation C0020626 Hypoparathyroidism HSDN C0027498 Nausea vomiting C1290138 Ssc without skin involvement MalaCards C1963087 Constipation adverse event C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0028738 Nystagmus C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C0042420 Vasovagal episode C1956346 Coronary artery disease HSDN C0031911 Pigment deposition C0153413 Malignant neoplasm of upper third of esophagus MalaCards C0009763 Conjunctiva inflammation C3152144 Agammaglobulinemia 1, autosomal recessive HPO C0917816 Deficiency mental C1856969 Epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders MalaCards C2203646 Jaundice C0242383 Age related macular degeneration HSDN C0011991 Loose stools C1837329 Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema MalaCards C3898969 Have been vomiting C0036202 Sarcoidosis HSDN C0004604 Pain back C0009319 Colitis HSDN C0018772 Deafness C0796121 Primrose syndrome MalaCards|HPO C0581394 Lower extremity swelling C0036220 Kaposi sarcoma UMLS C0019209 Large liver C0041234 Chagas disease OrphaNet|MalaCards C3887638 Failure to thrive in infant C1959626 Mevalonic aciduria MalaCards|HPO C1963071 Back pain adverse event C0031149 Peritoneal neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018920 Hemangioma, cavernous HSDN C0040822 D tremors C2677326 Epileptic encephalopathy, early infantile, 4 MalaCards|HPO|UMLS C4084788 Have dizziness C0005424 Biliary tract diseases HSDN C2984058 Have pain C0026766 Multiple organ failure HSDN C0015230 Exanthem C0016632 Fox-fordyce disease UMLS C2984057 Have nausea C1963274 Vasculitis adverse event HSDN C0042025 Urinary incontinence stress C0282488 Interstitial cystitis HSDN C0002965 Crescendo angina C0023890 Liver cirrhosis HSDN C0424755 Fever symptoms C0032987 Ectopic pregnancy HSDN C1963252 Tremor adverse event C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0019209 Large liver C3537440 Cystinosis, infantile nephropathic MalaCards C2242996 Tingling C0022661 Kidney failure, chronic HSDN C0013595 Eczematous dermatitis C1842485 Zinc in breast milk, reduced HPO C0027796 Neuralgias C3850024 Transcranial direct current stimulation HSDN C2911647 Weight gain adverse event C0010346 Crohn disease HSDN C3887873 Hearing loss C0031212 Personality disorders HSDN C1856661 Cornea cloudy C0043459 Zellweger syndrome HPO C4085317 Diarrhea frequency C1253937 Pericardial effusion HSDN C0002962 Angina C0149721 Left ventricular hypertrophy HSDN C2010808 Generalized skin lesions including interior of rectum C0037284 Skin lesion UMLS C0242936 Center pain C0026766 Multiple organ failure HSDN C0015469 Facial paralysis C0035126 Reperfusion injury HSDN C0231218 Malaise generalized C0206698 Cholangiocarcinoma UMLS C0086439 Activity decreased C0027773 Nesidioblastosis HSDN C4085210 Usual severity pain C0085136 Central nervous system neoplasms HSDN C1549543 Administration method - pain C0751772 Rem sleep behavior disorder HSDN C0728710 Pupil constriction observed C0027814 Neuritis, autoimmune, experimental HSDN C0019209 Large liver C0751202 Cystathionine beta-synthase deficiency disease HPO C0234132 Pyramidal sign C1849722 Polyglucosan body disease, adult form OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0024121 Lung neoplasms HSDN C0240735 Personality change C0085209 Bovine spongiform encephalitis MalaCards C0242936 Center pain C0016558 Forensic psychiatri HSDN C0013362 Dysarthrias C0268274 Gangliosidoses, gm2 HSDN C0030486 Extremity paralysis, lower C1962971 Myocarditis adverse event HSDN C4085222 Nausea C2984299 Asthma pathway HSDN C0013421 Dystonia C0037274 Dermatologic disorders HSDN C0424755 Fever symptoms C0554636 Canicola fever MalaCards C0030486 Extremity paralysis, lower C0700594 Radiculopathy HSDN C0022346 Yellow skin C4225242 Dehydrated hereditary stomatocytosis 2 UMLS C4042891 Sleep wake disorders C0004275 Attitude health HSDN C0019209 Large liver C0268312 Progressive intrahepatic cholestasis (disorder) OrphaNet|HPO C0427055 Face weakness C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards|UMLS C1557397 Adverse event associated with pain C0016548 Foreign body migration HSDN C2315100 Pediatric failure to thrive C0340427 Familial dilated cardiomyopathy MalaCards C0019209 Large liver C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C4084773 Bothered by weight gain C0017601 Glaucomas HSDN C0015469 Facial paralysis C0027868 Neuromuscular diseases HSDN C0018989 Paresis of one side of body C0035317 Retinal hemorrhage MalaCards C4084776 Weight loss C0033941 Psychoses, substance-induced HSDN C0040264 Ear ringing sound C2931176 Familial progressive vestibulo-cochlear dysfunction MalaCards C4085211 Pain distress question C0425045 Sudden infant death HSDN C0013404 Respiratory difficulty C0034186 Pyelonephritis HSDN C0917816 Deficiency mental C3805432 Cob1 MalaCards C0018520 Breath odor C0349231 Phobic anxiety disorder HSDN C1963071 Back pain adverse event C1704272 Benign prostatic hyperplasia HSDN C0242936 Center pain C0039131 Syphilis congenital HSDN C1963177 Muscle pain adverse event C4048826 Mud fever MalaCards C0232466 Feeding difficulty C3553529 Combined oxidative phosphorylation deficiency 10 MalaCards C0033377 Caudal displacement C0795941 Brachycephaly-deafness-cataract-microstomia-mental retardation syndrome MalaCards C1963086 Confusion adverse event C0997768 Glaucoma HSDN C1963077 Bone pain adverse event C2749484 Neuroblastoma, susceptibility to HPO C0030552 Paralysis partial C0282606 Myomatous neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042063 Urogenital abnormalities HSDN C4084776 Weight loss C0700327 Clinical findings relating to memory HSDN C0150055 Pain chronic C0393834 Diabetic chronic painful polyneuropathy UMLS C4084784 Diarrhea C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0018520 Breath odor C0004692 Balantidiasis MalaCards C0019209 Large liver C0037661 Somatostatinoma OrphaNet|MalaCards C0020305 Fetal edema C0042063 Urogenital abnormalities HSDN C0015672 Decreased energy C0023281 Leishmaniasis MalaCards C0034151 Hyperglobulinemic purpura C0034069 Pulmonary fibrosis HSDN C3539893 Pelvic pain occurs with intercourse C1956346 Coronary artery disease HSDN C4085211 Pain distress question C0042580 Vesico-ureteral reflux HSDN C0027498 Nausea vomiting C0243026 Sepsis UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0040947 Trichostrongyloidiasis HSDN C1963137 Hydrocephalus adverse event C1096902 Infantile sialic acid storage disease HPO C0018784 Deafness sensorineural C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria MalaCards C0030552 Paralysis partial C0022716 Menkes kinky hair syndrome OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0033860 Psoriasis HSDN C0028738 Nystagmus C1848932 Tapetoretinal degeneration with ataxia MalaCards C2237041 Shox gene with short stature C3554774 Tyshchenko syndrome MalaCards C2219867 Anxiety with excessive sweating C0003467 Anxiety UMLS C1963252 Tremor adverse event C1843264 Dystonia 13, torsion MalaCards C4084769 Vomiting frequency C2717906 Hereditary angioedema type i HPO C3539022 Pelvic pain decreasing in severity C0262655 Recurrent urinary tract infection HSDN C2203646 Jaundice C0392622 Toxic effect of carbon tetrachloride HSDN C3829611 Nausea frequency C0431109 Choroid plexus carcinoma HPO C1963086 Confusion adverse event C0153066 Murray valley encephalitis DiseaseOntology|MalaCards C4085317 Diarrhea frequency C0854795 Resectable hepatic malignant neoplasm MalaCards C0917816 Deficiency mental C0796059 Oculopalatoskeletal syndrome MalaCards C0018991 Paralysis one side of body C1835671 Axonal neuropathy with palmoplantar keratoderma MalaCards C0009676 Confusion state C1968835 Egot gene HSDN C0022346 Yellow skin C3899979 Bclc stage b hepatocellular carcinoma UMLS C0151686 Growth retardation C1859406 Borrone di rocco crovato syndrome MalaCards C4085211 Pain distress question C0015625 Fanconi anemia HSDN C3829611 Nausea frequency C1705811 Terminology role entity HSDN C1279888 Proteinuria of undiagnosed cause C0009241 Cognition disorders HSDN C4085222 Nausea C0242342 Sheehan syndrome OrphaNet|MalaCards C0522224 Palsied C2077203 Recurrent laryngeal nerve injuries HSDN C1263846 Attention deficit disorder with hyperactivity C0154629 Other specified manifestations of hyperkinetic syndrome MalaCards C0010200 Cough symptom C1623041 Breast-fed HSDN C0522224 Palsied C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C3665492 Pigmentations C3887678 Cpnet MalaCards C0012569 Double vision C0043251 Wounds and injuries HSDN C0242936 Center pain C0869332 Of water deprivation HSDN C0013362 Dysarthrias C0751785 Unverricht-lundborg syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0043541 Zygomycoses HSDN C0039239 Tachycardia sinus C0031511 Pheochromocytoma MalaCards C1549543 Administration method - pain C0009081 Congenital clubfoot HSDN C4084802 Usual severity diarrhea C0021847 Intestinal pseudo-obstruction HSDN C0009806 Constipate C3854315 Pseudoprimary hyperaldosteronism MalaCards C2203646 Jaundice C0035066 Renal artery obstruction HSDN C2984058 Have pain C0020625 Hyponatremia HSDN C0010520 Skin cyanosis C0080304 Vascular fistula HSDN C4084723 Constipation C1546847 Entity name part type - family HSDN C0003467 Angst C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C3815497 Cough C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C1963281 Vomiting adverse event C0020544 Renal hypertension HSDN C0012833 Dizzy C0016053 Fibromyalgia HSDN C0036572 Convulsion C0041341 Tuberous sclerosis OrphaNet|HPO C1963091 Diarrhea adverse event C1690964 Cataract HSDN C3815497 Cough C0024525 Malacoplakia MalaCards C2984057 Have nausea C0003507 Aortic valve stenosis HSDN C0349489 Fetal hypoxia C0024115 Lung diseases HSDN C0332563 Papulae C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) OrphaNet|HPO|MalaCards C0005745 Blepharoptosis C3554079 Combined oxidative phosphorylation deficiency 12 MalaCards C0020672 Body temperature decreased C0011854 Diabetes mellitus, insulin-dependent HSDN C0030193 Sense of pain C0016053 Fibromyalgia UMLS C0234979 Dysdiadochokinesia C1963674 Spinocerebellar ataxia 10 MalaCards|HPO|UMLS C0010200 Cough symptom C0162359 Christ-siemens-touraine syndrome OrphaNet|MalaCards C0020458 Hyperhydrosis C1832600 Naxos disease OrphaNet|HPO|MalaCards C0424755 Fever symptoms C0024630 Malingering HSDN C2984058 Have pain C0038862 Inflammation purulent HSDN C1384666 Decreased hearing C1999266 Depression adverse event HSDN C4085211 Pain distress question C3150878 Hyperoxaluria, primary, type iii MalaCards C0002962 Angina C0017185 Gastrointestinal neoplasms HSDN C0027497 Queasy C0019310 Hernia, obturator HSDN C0344315 Mood depressed C0242526 Gonadal dysgenesis, 45,x MalaCards C3887784 Decreased urine output C0812393 Cancer patients and suicide and depression HSDN C4085661 Usual severity nausea C0042164 Uveitis HSDN C0518090 Frequency of pain question C0243001 Abdominal abscess HSDN C0012569 Double vision C0152177 Trigeminal neuropathy HSDN C2984058 Have pain C0002880 Autoimmune hemolytic anemia HSDN C3641756 Have diarrhea C0086647 Mucopolysaccharidosis type iiia HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2020541 Strabismus HSDN C0042963 Symptoms vomiting C0009375 Colonic neoplasms HSDN C1313921 Urinomas C0221752 Rbc urine HSDN C0018772 Deafness C3150756 Chromosome 4q21 deletion syndrome MalaCards C0013428 Painful urination C0860239 Catheter infections related HSDN C0019209 Large liver C1861455 Stomatocytosis i HPO C0034642 Chest crepitation C0085786 Hamman-rich syndrome MalaCards C0018991 Paralysis one side of body C0042018 Urinary calculi HSDN C1963086 Confusion adverse event C0033375 Prolactinoma HSDN C0030552 Paralysis partial C0085436 Meningitis, cryptococcal HSDN C0013421 Dystonia C1843013 Alzheimer disease, familial, type 3 HPO C0151889 Reflexes tendon increased C3489725 Pseudo-torch syndrome OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0011875 Diabetic angiopathies HSDN C2911645 Weight loss adverse event C0597109 Nurse's role HSDN C0041834 Erythematous condition C0024137 Lupus erythematosus, cutaneous OrphaNet C0086437 Joint hypermobility C1834818 Mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones UMLS C0033774 Skin pruritus C0033771 Prurigo UMLS C1963274 Vasculitis adverse event C0004943 Behcet syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0015625 Fanconi anemia HSDN C0013421 Dystonia C0028064 Niemann-pick diseases MalaCards C0002962 Angina C0340629 Aortic aneurysm without mention of rupture nos HSDN C0042928 Paralysis vocal cord C0041310 Endocrine tuberculoses HSDN C0149793 Transient monocular blindness C0751955 Brain infarction HSDN C0040822 D tremors C1563215 Powassan encephalitis virus infection MalaCards C2024878 Cardiovascular surgery result: dyspnea C0031880 Obesity hypoventilation syndrome HSDN C0010200 Cough symptom C1711226 Pulmonary lymphomatoid granulomatosis UMLS C0018520 Breath odor C0006430 Burning mouth syndrome HSDN C0040822 D tremors C0040409 Tongue diseases HSDN C0151818 Opisthotonos C0268119 Combined molybdoflavoprotein enzyme deficiency HPO C4042891 Sleep wake disorders C0175702 Williams syndrome HSDN C0917816 Deficiency mental C3698541 Ohdo syndrome, maat-kievit-brunner type MalaCards C0151786 Weakness muscle C0035053 Spontaneous remission HSDN C4084776 Weight loss C0037354 Smallpox HSDN C3887638 Failure to thrive in infant C0023521 Globoid cell leukodystrophy MalaCards|HPO C2984058 Have pain C0149678 Epstein-barr virus infections HSDN C0000737 Abdomen pain C0346185 Dysgerminoma of ovary UMLS C0030554 Abnormal sensation C0006413 Burkitt lymphoma HSDN C3898969 Have been vomiting C0024228 Lymphatic diseases HSDN C0042963 Symptoms vomiting C0393735 Headache disorders HSDN C1962972 Proteinuria adverse event C0018802 Congestive heart failure HSDN C4084767 Bothered by vomiting C0040136 Thyroid neoplasm HSDN C2919142 Short stature adverse event C0796117 Pitt syndrome MalaCards C3829611 Nausea frequency C3888013 Hypnoses HSDN C3641756 Have diarrhea C0005940 Bone diseases HSDN C4084769 Vomiting frequency C0344434 Atrial fibrillation ecg HSDN C0242936 Center pain C1449861 Micronuclei, chromosome-defective HSDN C0005409 Bilharzial pigment deposition C0549567 Pigmentation disorders UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3539923 Cdisc adas-cog - orientation summary score HSDN C0036572 Convulsion C0018939 Hematological disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0033377 Caudal displacement C0032001 Pituitary apoplexy MalaCards C0013604 Edematous C0032580 Adenomatous polyposis coli HSDN C3827868 Tachycardia by ecg finding C0268474 Hydroxykynureninuria MalaCards|HPO C2984058 Have pain C0029883 Otitis media with effusion HSDN C2024893 Cardiovascular surgery result: fatigue C0036983 Septic shock HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0008728 Churg-strauss syndrome HSDN C0003862 Pain joint C0029436 Bone disease, disappearing HSDN C0239517 Face paresthesia C0362076 Head problem UMLS C0518090 Frequency of pain question C0035795 Fever mountain rocky spotted HSDN C4084775 Usual severity weight loss C0040997 Trigeminal neuralgia HSDN C0002962 Angina C0018915 Hemangioendothelioma HSDN C0038990 Sweats C0175693 Russell-silver syndrome MalaCards C0043094 Weight gain C3495559 Juvenile arthritis HSDN C1069915 Vertigo C0003864 Arthritis HSDN C0270948 Neurogenic muscular atrophy C3150973 Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degeneration and progressive polyneuropathy type) MalaCards|HPO C0242936 Center pain C0018081 Gonorrhea HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0700095 Central neuroblastoma HSDN C2077296 Insomnia due to environmental disturbances C0752289 Environmental sleep disorder UMLS C0349588 Stature short C3540845 Microphthalmia, isolated, with coloboma 8 MalaCards C0036572 Convulsion C0024228 Lymphatic diseases HSDN C0015672 Decreased energy C0007786 Brain ischemia HSDN C0027498 Nausea vomiting C0042111 Urticaria pigmentosa OrphaNet|MalaCards C0424755 Fever symptoms C0026277 Mixed salivary gland tumor HSDN C2984058 Have pain C0024525 Malacoplakia HSDN C0030552 Paralysis partial C0235032 Neurotoxicity syndromes HSDN C0015672 Decreased energy C3814778 Hemolytic index HSDN C0008031 Pain chest C0152171 Idiopathic pulmonary hypertension OrphaNet C1963091 Diarrhea adverse event C0019655 Histoplasmosis HSDN C1384666 Decreased hearing C0008441 Chondroblastoma HSDN C4085211 Pain distress question C0036420 Localized scleroderma HSDN C0031154 Peritonitis, nos C0031069 Familial mediterranean fever HPO C0162298 Stiffness joints C1869114 Weill-marchesani syndrome, autosomal recessive HPO|UMLS C0030486 Extremity paralysis, lower C0032987 Ectopic pregnancy HSDN C0349588 Stature short C1862103 Brachydactyly type c MalaCards|HPO C0005745 Blepharoptosis C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0013362 Dysarthrias C3711370 Spastic paraplegia type 7 MalaCards C0042571 Vertigo subjective C0003490 Aortic arch syndrome HSDN C3815497 Cough C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0007758 Cerebellar ataxia C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards C4084726 Distress cough C4050613 Anxiety scale (basc-2) HSDN C3539023 Pelvic pain increasing in frequency C0684743 Malignant neoplasm of muscle HSDN C1000483 Genus anemia C2749484 Neuroblastoma, susceptibility to HPO C3539891 Pelvic pain to the rear C0011854 Diabetes mellitus, insulin-dependent HSDN C0085636 Light sensitivity C1864900 Retinal cone dystrophy 3a HPO|UMLS C1557397 Adverse event associated with pain C0036920 Sezary syndrome HSDN C0152200 Achromatism C1849792 Achromatopsia 3 MalaCards|HPO C1510456 Wernicke aphasia C0160680 Carotid artery injury HSDN C4085211 Pain distress question C0042487 Venous thrombosis HSDN C2242996 Tingling C1956390 Cranial arteritis MalaCards C0542476 Forgetful C1843013 Alzheimer disease, familial, type 3 HPO C0007166 Cardiac output decreased C1963138 Hypertension adverse event HSDN C0013404 Respiratory difficulty C0020437 Hypercalcemia HSDN C0085636 Light sensitivity C0343057 Keratosis pilaris decalvans HPO C4084724 Usual severity constipation C0026266 Mitral valve insufficiency HSDN C2919142 Short stature adverse event C3554042 Dba11 MalaCards C0036572 Convulsion C0042514 Tachycardia, ventricular HSDN C3665492 Pigmentations C1848410 Xeroderma pigmentosum, variant type MalaCards C4084788 Have dizziness C4049994 Insulin resistance measurement HSDN C0011991 Loose stools C0018213 Graves disease HSDN C4084725 Usual severity cough C0018802 Congestive heart failure HSDN C0344232 Blurred vision C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C0013428 Painful urination C0040553 Toxocariasis HSDN C0398650 Idiopathic thrombocytopenia purpura C1999266 Depression adverse event HSDN C4084768 Usual severity vomiting C0020445 Hypercholesterolemia, familial HSDN C0027066 Myoclonic jerking C0023788 Whipple disease OrphaNet|MalaCards C0036572 Convulsion C0270857 Epilepsy, reflex UMLS C0033377 Caudal displacement C1852406 Cutis gyrata syndrome of beare and stevenson OrphaNet|HPO|MalaCards C0018772 Deafness C0037369 Smoking HSDN C1963087 Constipation adverse event C0011071 Sudden death HSDN C0013404 Respiratory difficulty C0042109 Urticaria HSDN C4084766 Vomiting C0020523 Immediate hypersensitivity HSDN C0018991 Paralysis one side of body C2931029 Nevi flammei, familial multiple HPO C0030193 Sense of pain C0030521 Parathyroid neoplasms HSDN C0032285 Pneum C0086438 Hypogammaglobulinemia OrphaNet|MalaCards C0700590 Diaphoresis excessive C3810072 Palmoplantar keratoderma, nagashima type MalaCards C0002962 Angina C0018809 Heart neoplasm HSDN C4042891 Sleep wake disorders C0001144 Acne vulgaris HSDN C0026821 Cramp C0005424 Biliary tract diseases HSDN C4085211 Pain distress question C0032797 Postpartum hemorrhage HSDN C0020796 Profoundly mentally retarded C3151461 Lis4 MalaCards|HPO C0518090 Frequency of pain question C0006105 Brain abscess HSDN C4084767 Bothered by vomiting C3463824 Myelodysplastic syndrome HSDN C4085862 Bothered by nausea C1963106 Esophagitis adverse event HSDN C3641755 Have constipation C0022758 Kap HSDN C0349489 Fetal hypoxia C0035344 Retinopathy of prematurity HSDN C0344232 Blurred vision C0014805 Primary erythermalgia MalaCards|HPO|UMLS C2984058 Have pain C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0349588 Stature short C0025237 Melnick-needles syndrome MalaCards C0030552 Paralysis partial C0043046 Wasting syndrome HSDN C2315100 Pediatric failure to thrive C0028968 Olivopontocerebellar atrophies HSDN C0030232 Color loss C2676137 Diamond-blackfan anemia 1 MalaCards|HPO C0018965 Blood urine C0272295 Purpura, rheumatica MalaCards C4084724 Usual severity constipation C0268242 Niemann-pick disease, type a MalaCards|HPO C0392699 Dysaesthesia C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C0009806 Constipate C0037019 Shy-drager syndrome HSDN C0018834 Brash C3554209 Pontocerebellar hypoplasia, type 8 MalaCards C0587050 Lower extremity mass C0574043 Foot ganglion UMLS C0028738 Nystagmus C3888001 Hermansky-pudlak syndrome 3 MalaCards C0030193 Sense of pain C0037054 Sickle cell trait MalaCards|HSDN C0013595 Eczematous dermatitis C1864186 Cdags syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0002726 Amyloidosis HSDN C0002170 Alopecia disorders C3151468 Palmoplantar keratoderma and congenital alopecia 1 HPO C3463815 Feel fatigue C2984291 Glioblastoma multiforme pathway HSDN C4084802 Usual severity diarrhea C0342288 Insulin-dependent diabetes mellitus secretory diarrhea syndrome MalaCards|HPO C1963281 Vomiting adverse event C0162532 Variegate porphyria MalaCards|HPO C0036396 Sciatica C0005940 Bone diseases HSDN C0151686 Growth retardation C2931745 Ladda zonana ramer syndrome MalaCards C2911645 Weight loss adverse event C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C2237041 Shox gene with short stature C1968741 Gsd iiic HPO C0043094 Weight gain C0001430 Adenoma HSDN C4085862 Bothered by nausea C0036875 Disorders of sex development HSDN C1963091 Diarrhea adverse event C0011311 Dengue fever MalaCards|HSDN C0040034 Thrombocytopenia C3151785 Anemia, x-linked, without thrombocytopenia HPO C0042963 Symptoms vomiting C0853697 Neutrophil count decreased HSDN C0349588 Stature short C3278138 Fibrochondrogenesis 1 MalaCards C0270948 Neurogenic muscular atrophy C2678061 Scapuloperoneal myopathy, x-linked dominant MalaCards|HPO C0857305 Thrombocytopenia purpura C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4085317 Diarrhea frequency C0023241 Legionnaires' disease MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C4084769 Vomiting frequency C0019054 Hemolysis (disorder) HSDN C3539893 Pelvic pain occurs with intercourse C0033578 Prostatic neoplasms HSDN C0413252 Hypothermia due to exposure C0034531 Experimental radiation injuries HSDN C3641756 Have diarrhea C0206526 Tuberculosis, multidrug-resistant HSDN C0036572 Convulsion C0037578 Soft tissue injury HSDN C0242936 Center pain C0022575 Keratoconjunctivitis sicca HSDN C4085549 Dizziness C2609414 Acute kidney injury HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040948 Trichostrongyliasis HSDN C3665346 Loss sight C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C4084802 Usual severity diarrhea C3714580 Hypokalemic periodic paralysis type 1 HSDN C0349588 Stature short C1961835 Gaucher disease, type 1 MalaCards C0349588 Stature short C0406587 Wrinkly skin syndrome MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C3280845 Charcot-marie-tooth disease, dominant intermediate e MalaCards C4084775 Usual severity weight loss C0013274 Patent ductus arteriosus HSDN C0036572 Convulsion C3150215 Chromosome 6q24-q25 deletion syndrome MalaCards C0036572 Convulsion C0034531 Experimental radiation injuries HSDN C4084788 Have dizziness C0010068 Coronary heart disease HSDN C1384666 Decreased hearing C1962979 Burn adverse event HSDN C0014591 Bleeding nose C3150889 Factor v and factor viii, combined deficiency of, 2 HPO C0497247 Blood pressure elevation C0342881 Familial hypercholesterolemia - homozygous OrphaNet|HPO|MalaCards C0426579 Anorexia symptom C1963106 Esophagitis adverse event HSDN C4084727 Cough frequency C0021831 Intestinal diseases HSDN C0003550 Broca aphasia C0085084 Motor neuron disease HSDN C0040822 D tremors C0020550 Hyperthyroidism HSDN C0016382 Cutaneous vascular engorgement C1866560 Iridogoniodysgenesis, type 1 (disorder) MalaCards C1579931 Depressed - symptom C1834846 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 HPO C0009421 Comatose C0014394 Enuresis HSDN C0022346 Yellow skin C0268353 Cutis laxa, x-linked MalaCards C2237041 Shox gene with short stature C0406727 Orofaciodigital syndrome 4 MalaCards|HPO C4085661 Usual severity nausea C0002736 Amyotrophic lateral sclerosis HSDN C3539892 Pelvic pain in front C0041582 Ulcer HSDN C0576456 Poor feeding C0025517 Metabolic diseases MalaCards C0012833 Dizzy C0003507 Aortic valve stenosis HSDN C1557397 Adverse event associated with pain C0039373 Tay-sachs disease HSDN C2919142 Short stature adverse event C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C0036572 Convulsion C0796202 Wittwer syndrome MalaCards C0040264 Ear ringing sound C0563150 Catastrophization HSDN C4085211 Pain distress question C0024228 Lymphatic diseases HSDN C4085317 Diarrhea frequency C0003125 Anorexia nervosa HSDN C1069915 Vertigo C1136041 Familial acoustic neuroma OrphaNet|HPO C1963180 Neck pain adverse event C0031154 Peritonitis HSDN C1963086 Confusion adverse event C0595888 Phosphate serum decreased HSDN C2237041 Shox gene with short stature C0265354 Charge syndrome MalaCards C0030552 Paralysis partial C0391817 Drug-induced autoim haem anaem OrphaNet|MalaCards C0013404 Respiratory difficulty C0017638 Glioma HSDN C0030193 Sense of pain C3899648 Childhood paranasal sinus carcinoma UMLS C0009421 Comatose C0004377 Automatism HSDN C0013421 Dystonia C2930900 Beta-sarcoglycanopathy MalaCards C0151786 Weakness muscle C0524909 Hepatitis b, chronic HSDN C0000727 Abdomen acute C0878544 Cardiomyopathies HSDN C0221752 Rbc urine C0268389 Amyloidosis, familial visceral MalaCards|HPO C1962972 Proteinuria adverse event C0026363 Mohr-claussen syndrome MalaCards C2188458 Urinary incontinence without sensory awareness of wetness C0042024 Urinary incontinence UMLS C3665347 Vision impaired C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C2752007 Congenital disorder of glycosylation, type io MalaCards C0340288 Angina stable C0021368 Inflammation HSDN C2984057 Have nausea C0018939 Hematological disease HSDN C0349588 Stature short C0265343 Jarcho-levin syndrome OrphaNet|HPO C4084725 Usual severity cough C0919267 Ovarian neoplasm HSDN C0557874 Global developmental delay C1956093 Paris-trousseau thrombocytopenia MalaCards C0040460 Dental pain C0030305 Pancreatitis HSDN C1963164 Lymphopenia adverse event C2936664 Acquired hypogammaglobulinemia MalaCards C4084723 Constipation C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C0009421 Comatose C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0009421 Comatose C1962979 Burn adverse event HSDN C0033776 Pregnancy and pruritus C2103069 Non-infectious skin disorders UMLS C0013404 Respiratory difficulty C0518450 Spinal fractures HSDN C4085661 Usual severity nausea C0007786 Brain ischemia HSDN C0007859 Pain neck C0035302 Retinal artery occlusion HSDN C4084775 Usual severity weight loss C0018790 Cardiac arrest HSDN C0036572 Convulsion C0010276 Craniopharyngioma MalaCards|HPO C0018926 Emesis bloody C0027809 Neurilemmoma HSDN C0751495 Seizure focal C0014118 Endocarditis UMLS C0011991 Loose stools C0034929 Reflex HSDN C0917816 Deficiency mental C1858477 Epilepsy, partial, with variable foci HPO C0232466 Feeding difficulty C0268581 Holocarboxylase synthetase deficiency MalaCards C0039070 Collapse fleeting C0340850 Neurally-mediated syncope UMLS C1090821 Sepsis C2931876 Hirschsprung disease 1 MalaCards C0030552 Paralysis partial C0003493 Aortic diseases HSDN C0026838 Spasticity muscle C0265962 Ichthyosis linearis circumflexa MalaCards C2919142 Short stature adverse event C1833603 Spondyloepiphyseal dysplasia with atlantoaxial instability MalaCards C0241898 Generalized fatigue C1852529 Corticosteroid-binding globulin deficiency MalaCards|UMLS C4084769 Vomiting frequency C0003469 Anxiety disorders HSDN C0001825 Agraphia C0007274 Carotid artery thrombosis HSDN C1963087 Constipation adverse event C0006145 Breast diseases HSDN C4084767 Bothered by vomiting C0017128 Fistula gastric HSDN C0031911 Pigment deposition C4072980 Exudative vitreoretinopathy MalaCards C0018772 Deafness C2677590 Congenital disorder of glycosylation, type in OrphaNet|HPO|MalaCards C0013608 Cardiac edema C0007177 Cardiac tamponade HSDN C0241137 Skin pallor C0162835 Hypopigmentation disorder HSDN C1384666 Decreased hearing C2751651 Chromosome 19q13.11 deletion syndrome MalaCards C4085211 Pain distress question C0021841 Intestinal neoplasms HSDN C4084766 Vomiting C0460137 Push down or depress HSDN C0042024 Urine incontinence C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0018784 Deafness sensorineural C3809522 Infantile liver failure syndrome 1 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0236969 Substance-related disorders HSDN C0002622 Amnesias C1858991 Childhood ataxia with central nervous system hypomyelinization MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1555914 Psychologist - psychotherapy, group HSDN C0009398 Color vision defects C0043251 Wounds and injuries HSDN C2129056 Frequency of urination during night C0028734 Nocturia UMLS C0013604 Edematous C0006109 Brain damage, chronic HSDN C4084788 Have dizziness C0524910 Hepatitis c, chronic HSDN C0030975 Disorders perception C0002871 Anemia HSDN C3898969 Have been vomiting C2984291 Glioblastoma multiforme pathway HSDN C4084776 Weight loss C0012644 Animal disease models HSDN C0018784 Deafness sensorineural C0038160 Staphylococcal infections HSDN C0973461 Dysphasia C0431406 Asymmetric crying face association OrphaNet|HPO C0851578 Disorder sleep C0011609 Drug eruptions HSDN C0042024 Urine incontinence C0019202 Hepatolenticular degeneration HSDN C1963091 Diarrhea adverse event C0001529 Dercum disease MalaCards C4085317 Diarrhea frequency C0015300 Exophthalmos HSDN C0151786 Weakness muscle C0085220 Cerebral amyloid angiopathy HSDN C0460137 Push down or depress C0795953 Masa syndrome (disorder) MalaCards C0242936 Center pain C0020295 Hydronephrosis HSDN C0024031 Back pain lower back C0027746 Nerve degeneration HSDN C1963091 Diarrhea adverse event C0018213 Graves disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0033873 Psychiatry HSDN C0013395 Indigestion C0036677 Sensory threshold HSDN C0042963 Symptoms vomiting C0518450 Spinal fractures HSDN C4084784 Diarrhea C1000587 Pemphigus HSDN C0344435 Ventricular fibrillation by ecg finding C2751830 Long qt syndrome 12 MalaCards|HPO C0451941 Itch scrotum C1290866 Disease of pelvis UMLS C0085632 Listlessness C1858991 Childhood ataxia with central nervous system hypomyelinization MalaCards|UMLS C0042755 Virilisation C4049644 Depression HSDN C0040822 D tremors C0022802 Kuru HSDN C4085222 Nausea C0600564 Self-efficacy HSDN C0007166 Cardiac output decreased C0038454 Cerebrovascular accident HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2931642 Benign symmetrical lipomatosis HSDN C3494358 Characteristic, prodromal C0011570 Mental depression HSDN C0037763 Spasm C0007097 Carcinomas HSDN C3665492 Pigmentations C0265407 Chromosome 4 ring syndrome MalaCards C0349588 Stature short C4015558 Temple syndrome MalaCards C0033774 Skin pruritus C0000833 Abscess HSDN C0024031 Back pain lower back C0018802 Congestive heart failure UMLS C4084802 Usual severity diarrhea C0029445 Bone necrosis HSDN C4084774 Have weight loss C0085632 Apathy HSDN C0030193 Sense of pain C0085409 Polyendocrinopathies, autoimmune HSDN C0042420 Vasovagal episode C0034929 Reflex HSDN C1963087 Constipation adverse event C0423742 Intercourse pain HSDN C1279888 Proteinuria of undiagnosed cause C0033817 Pseudomonas infections HSDN C0030486 Extremity paralysis, lower C0016171 Fistula of intestine, excluding rectum and anus HSDN C1549543 Administration method - pain C0021568 Bites insect stings HSDN C2984058 Have pain C0702094 Agranulocytosis lab result HSDN C0023012 Delay language C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C0019209 Large liver C3489789 Cholestasis, progressive familial intrahepatic, 2 MalaCards C4084766 Vomiting C0342784 Pearson's marrow-pancreas syndrome HPO C0042963 Symptoms vomiting C1704212 Embolism embolus HSDN C0010038 Corneal opacity disorder C0029434 Osteogenesis imperfecta OrphaNet C0018681 Headache, cephalalgia C0026780 Mumps MalaCards C0018777 Deafness, conductive C0027859 Acoustic neuroma HSDN C0476273 Distress respiratory C0345160 Congenital laryngomalacia MalaCards C4085549 Dizziness C0000735 Abdominal neoplasms HSDN C0020673 Hypothermia (central) (local) C0007193 Cardiomyopathy, dilated HSDN C2029884 Hearing loss by exam C0015398 Eye diseases, hereditary HSDN C1279888 Proteinuria of undiagnosed cause C0086922 Purpura rheumatoid MalaCards C0041657 Consciousness loss C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0042024 Urine incontinence C0156409 Atrophic vaginitis HSDN C4084726 Distress cough C0042138 Uterine neoplasms HSDN C4084784 Diarrhea C0019189 Hepatitis, chronic HSDN C1963252 Tremor adverse event C1838192 Spastic paraplegia 6, autosomal dominant (disorder) MalaCards|HPO C4084727 Cough frequency C0024141 Lupus erythematosus, systemic HSDN C0019214 Hepatosplenomegaly C1274233 T-lymphocyte immunodeficiency MalaCards C4085862 Bothered by nausea C3163620 Hypotension adverse event HSDN C0017181 Gastrointestinal bleed C0431406 Asymmetric crying face association HPO C0012569 Double vision C3163843 Chondrosarcoma of bone HSDN C4084802 Usual severity diarrhea C0034929 Reflex HSDN C0151686 Growth retardation C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C0018991 Paralysis one side of body C0011884 Diabetic retinopathy HSDN C0039070 Collapse fleeting C0812341 Latex allergy response UMLS C4084724 Usual severity constipation C0238015 Autonomic dysreflexia HSDN C0015970 Fever unknown origin C0023890 Liver cirrhosis HSDN C0024031 Back pain lower back C1963067 Atrial fibrillation adverse event HSDN C1963063 Anorexia adverse event C0017689 Glucagonoma OrphaNet|MalaCards C0314719 Dry eyes C0155082 Keratoconjunctivitis sicca, not specified as sjogren's UMLS C0162298 Stiffness joints C0342282 Symphalangism-brachydactyly syndrome MalaCards C4084725 Usual severity cough C0079487 Helicobacter infections HSDN C0233844 Awkwardness C1868576 Paroxysmal tonic upgaze, benign childhood, with ataxia MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0014534 Epididymitis HSDN C1963091 Diarrhea adverse event C0027092 Myopia HSDN C2896460 Limb pain right toe C0810058 Other connective tissue disease UMLS C0518090 Frequency of pain question C3163843 Chondrosarcoma of bone HSDN C0851578 Disorder sleep C0001529 Dercum disease MalaCards C0019521 Hiccoughs C0039144 Syringomyelia HSDN C4084775 Usual severity weight loss C0860549 Refeed syndrome HSDN C0035229 Respiratory function impaired C2678367 Renal tubular dysgenesis with choanal atresia and athelia HPO C0009421 Comatose C0032268 Pneumocephalus HSDN C3541349 Syncope C1623041 Breast-fed HSDN C1557397 Adverse event associated with pain C0007785 Cerebral infarction HSDN C0013395 Indigestion C0027726 Nephrotic syndrome HSDN C2911645 Weight loss adverse event C0037356 Smallpox virus HSDN C0011991 Loose stools C0267659 Raw-milk associated diarrhea UMLS C4084725 Usual severity cough C0037939 Spinal neoplasms HSDN C3641756 Have diarrhea C0024116 Lung diseases, fungal HSDN C0027497 Queasy C0011119 Decompression sickness HSDN C3665492 Pigmentations C1261473 Sarcoma MalaCards C0015230 Exanthem C0268323 Familial porphyria cutanea tarda MalaCards C2911647 Weight gain adverse event C0020732 Iatrogenic disease HSDN C4085548 Usual severity dizziness C0042510 Ventricular fibrillation HSDN C0423713 Ilioinguinal nerve neuralgia C0270891 Nerve plexus disorder, nos UMLS C0917816 Deficiency mental C0265265 Aase syndrome MalaCards|HPO C2237041 Shox gene with short stature C3179194 Galns deficiency MalaCards C0035229 Respiratory function impaired C1842025 Glaucoma and sleep apnea OrphaNet|MalaCards C0518090 Frequency of pain question C0002438 Amebiasis HSDN C1963091 Diarrhea adverse event C0014121 Bacterial endocarditis HSDN C3898969 Have been vomiting C0206644 Histiocytoma, benign fibrous HSDN C2237041 Shox gene with short stature C0268418 Deficiency of glycerol kinase OrphaNet|HPO|MalaCards C0030552 Paralysis partial C1839259 Bulbo-spinal atrophy, x-linked HSDN C1963091 Diarrhea adverse event C0002871 Anemia HSDN C2024893 Cardiovascular surgery result: fatigue C0517555 Venous thrombosis after immobility HSDN C4084726 Distress cough C0279626 Squamous cell carcinoma of esophagus OrphaNet|HPO|MalaCards C2984058 Have pain C0032966 Complication, neoplastic pregnancy HSDN C0004604 Pain back C1862092 Brachydactyly-distal symphalangism syndrome MalaCards C0013404 Respiratory difficulty C0035522 Rib fracture HSDN C3714552 Strength decreased C1855849 Bartter syndrome, antenatal , type 2 UMLS C0242936 Center pain C0085094 Head injury closed HSDN C4085211 Pain distress question C0016436 Folliculitis HSDN C0018991 Paralysis one side of body C0024535 Malaria, falciparum HSDN C0034150 Skin purpura C1145670 Respiratory failure HSDN C0237849 Skin desquamation C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C1557397 Adverse event associated with pain C0011269 Dementia, vascular HSDN C2024893 Cardiovascular surgery result: fatigue C0029445 Bone necrosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035455 Rhinitis HSDN C4085211 Pain distress question C0017920 Glycogen storage disease type i HSDN C4084776 Weight loss C0040156 Thyrotoxicosis MalaCards|HSDN C2919142 Short stature adverse event C2678045 Toe syndactyly, telecanthus, and anogenital and renal malformations OrphaNet|HPO C0018681 Headache, cephalalgia C2984302 Leishmaniasis infection pathway HSDN C0003467 Angst C0085209 Bovine spongiform encephalitis MalaCards C0003862 Pain joint C0524909 Hepatitis b, chronic MalaCards C0005745 Blepharoptosis C1739094 Foodborne botulism OrphaNet|MalaCards C1557397 Adverse event associated with pain C0039504 Injuries tendon HSDN C0019209 Large liver C0024748 Alpha-mannosidosis OrphaNet|HPO C0518090 Frequency of pain question C0003723 Arbovirus infections HSDN C2237041 Shox gene with short stature C0796088 Neurofaciodigitorenal syndrome OrphaNet|MalaCards C0234146 Absent reflex C1834339 Myopathy, actin, congenital, with excess of thin myofilaments HPO C0015672 Decreased energy C0041374 Tumor virus infections HSDN C0037763 Spasm C0034065 Pulmonary embolism HSDN C0332606 Facies elfin C0271689 Insulin receptor, defect in HPO C4085549 Dizziness C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C2036542 Stuttering interfering with family interaction C0038506 Stuttering UMLS C1963252 Tremor adverse event C0242287 Isaacs syndrome HPO C0009806 Constipate C1333867 Grade 1 colorectal adenocarcinoma UMLS C0027497 Queasy C3536715 Aa amyloidosis MalaCards C0012569 Double vision C0032533 Polymyalgia rheumatica MalaCards C3898969 Have been vomiting C0026782 Mumps vaccine HSDN C1963137 Hydrocephalus adverse event C2676790 Meckel syndrome, type 6 (disorder) HPO C4085210 Usual severity pain C0235833 Congenital diaphragmatic hernia HSDN C0030193 Sense of pain C0009373 Colonic diseases HSDN C0015230 Exanthem C0854839 Recurrent angioimmunoblastic t-cell lymphoma UMLS C0557874 Global developmental delay C1853623 Fryns-aftimos syndrome MalaCards C0423742 Intercourse pain C0033375 Prolactinoma OrphaNet|HPO|MalaCards C2242996 Tingling C0020626 Hypoparathyroidism HSDN C0015230 Exanthem C0031736 Polymorphous light eruption UMLS C0012833 Dizzy C1527406 Rhizomelic pseudopolyarthritis MalaCards C0000737 Abdomen pain C2931838 Familial hdl deficiency MalaCards C4084775 Usual severity weight loss C0035229 Respiratory insufficiency HSDN C0518090 Frequency of pain question C1368355 Synostosis malformation HSDN C3641756 Have diarrhea C0020517 Hypersensitivity HSDN C0156728 Edema or excessive weight gain in pregnancy no hypertension C0269672 Weight gain pregnancy excessive UMLS C0085636 Light sensitivity C0271270 Oculovestibuloauditory syndrome MalaCards C1963184 Nystagmus adverse event C1135161 Stage 4s neuroblastoma MalaCards C4084767 Bothered by vomiting C0342701 Transcobalamin ii deficiency MalaCards C2029884 Hearing loss by exam C0014065 Congenital cerebral hernia HSDN C4085222 Nausea C0020443 Hypercholesterolemia HSDN C1838869 Proximal neurogenic muscle weakness C0017921 Glycogen storage disease type ii MalaCards|HPO C0030554 Abnormal sensation C0021141 Inappropriate adh syndrome HSDN C0497406 Over weight C0270611 Brain damage HSDN C2362324 Pediatric obesity C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0036572 Convulsion C0020545 Hypertension, renovascular HSDN C0036572 Convulsion C1135161 Stage 4s neuroblastoma MalaCards C0002963 Angina variant C0085404 Poems syndrome HSDN C0278152 Hemifacial spasms C0003469 Anxiety disorders HSDN C3641755 Have constipation C0524910 Hepatitis c, chronic HSDN C4085862 Bothered by nausea C0025427 Mercury poisoning OrphaNet|MalaCards C0013604 Edematous C0002949 Aneurysm, dissecting HSDN C0022346 Yellow skin C0345904 Malignant neoplasm of liver MalaCards C0027498 Nausea vomiting C0264743 Rheumatic fever without heart involvement MalaCards C4084768 Usual severity vomiting C0079631 Interdisciplinary communication HSDN C0026826 High muscle tone C2931416 Fara chlupackova syndrome OrphaNet|HPO C0009806 Constipate C0002395 Alzheimer's disease HSDN C0022346 Yellow skin C0268608 Deficiency of dihydrofolate reductase MalaCards C3641756 Have diarrhea C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C4084774 Have weight loss C0039538 Teratoma HSDN C4085661 Usual severity nausea C0012691 Dislocations HSDN C0239181 Diarrhea intermittent C0153463 Malig neop oth spec pancreas MalaCards C0006370 Bulimia C0525045 Mood disorders HSDN C0036572 Convulsion C0020507 Hyperplasia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0949691 Spondylarthropathies HSDN C0018784 Deafness sensorineural C0006277 Bronchitis HSDN C2315100 Pediatric failure to thrive C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive MalaCards C2911645 Weight loss adverse event C0040046 Thrombophlebitis HSDN C0000737 Abdomen pain C0038354 Stomach diseases UMLS C3539895 Pelvic pain occurs with bowel movement C0019310 Hernia, obturator HSDN C4084776 Weight loss C0206629 Pulmonary blastoma OrphaNet|MalaCards C0085636 Light sensitivity C1854180 Cone-rod dystrophy 8 (disorder) MalaCards C4084802 Usual severity diarrhea C0003838 Arterial occlusive diseases HSDN C0023380 Lethargy C0023092 Lassa fever MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0032966 Complication, neoplastic pregnancy HSDN C4084774 Have weight loss C0030567 Parkinson disease HSDN C2237041 Shox gene with short stature C1849088 Spinocerebellar ataxia with dysmorphism OrphaNet C2919142 Short stature adverse event C3805879 Precocious puberty, central, 1 MalaCards C0917816 Deficiency mental C1845526 Mental retardation, x-linked 46 HPO C4085548 Usual severity dizziness C0037052 Sick sinus syndrome HSDN C0042025 Urinary incontinence stress C0597109 Nurse's role HSDN C0086565 Liver function abnormal C0040560 Toxoplasmosis, congenital MalaCards C0007758 Cerebellar ataxia C3151476 Mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MalaCards|HPO C4084766 Vomiting C1546949 Event consequence - death HSDN C0030193 Sense of pain C2985290 Fetal alcohol spectrum disorders HSDN C1384666 Decreased hearing C0031212 Personality disorders HSDN C1963184 Nystagmus adverse event C1856113 Mowat-wilson syndrome MalaCards C0018784 Deafness sensorineural C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C0015672 Decreased energy C0035613 Rift valley fever OrphaNet|MalaCards C0026838 Spasticity muscle C1963059 Adrenal insufficiency adverse event HSDN C0085128 Cardiac output elevated C0039231 Tachycardia HSDN C1963177 Muscle pain adverse event C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards C0013362 Dysarthrias C1846492 Spinocerebellar ataxia, autosomal recessive 4 MalaCards C0018777 Deafness, conductive C0796012 Krause-kivlin syndrome HPO C0020672 Body temperature decreased C0005974 Bone resorption HSDN C0085631 Abnormal excitement C0032787 Postoperative complications HSDN C0040822 D tremors C1848533 Ataxia with vitamin e deficiency HPO C0557874 Global developmental delay C0796081 Growth mental deficiency syndrome of myhre MalaCards C0240941 Scalp pruritus C0027822 Neurodermatitis UMLS C0014724 Burping C0013473 Eating disorders HSDN C0042571 Vertigo subjective C0155518 Hypoactive labyrinth-bilateral UMLS C2128726 Distal right leg soft tissue swelling C0037580 Soft tissue swelling UMLS C0018681 Headache, cephalalgia C0011168 Deglutition disorders UMLS C0018681 Headache, cephalalgia C0022667 Papillary necrosis HSDN C0858922 Shifting vision C0085635 Photopsia UMLS C0007758 Cerebellar ataxia C0268247 Niemann-pick disease, type d MalaCards|HPO C0030486 Extremity paralysis, lower C0011168 Deglutition disorders HSDN C1549543 Administration method - pain C0036117 Salmonella infections HSDN C0018784 Deafness sensorineural C0024904 Mastoiditis HSDN C0034150 Skin purpura C0018944 Hematoma HSDN C0812426 Kidney problem C0238143 Glomerulonephritis proliferative focal UMLS C0030552 Paralysis partial C0036421 Systemic scleroderma MalaCards C0016382 Cutaneous vascular engorgement C0024137 Lupus erythematosus, cutaneous OrphaNet C1549543 Administration method - pain C0018572 Hand, foot and mouth disease HSDN C0151686 Growth retardation C3536984 Vitamin d-resistant rickets, x-linked MalaCards C1963281 Vomiting adverse event C0268322 Chester-type porphyria HPO C0028738 Nystagmus C0268496 Kramer syndrome OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0032927 Precancerous conditions HSDN C1963065 Apnea adverse event C0009244 Behavioral cognitive therapy HSDN C0497247 Blood pressure elevation C0342200 Endemic cretinism MalaCards C0018681 Headache, cephalalgia C0031485 Phenylketonurias HSDN C0018772 Deafness C1290398 Cerebral arterial aneurysm HSDN C4085222 Nausea C0012147 Dientamoebiases DiseaseOntology C0010520 Skin cyanosis C0018801 Heart failure HSDN C0085636 Light sensitivity C0036472 Scrub typhus OrphaNet|MalaCards C0860645 Bizarre dreams C0234458 Dream disorder UMLS C0001825 Agraphia C0271270 Oculovestibuloauditory syndrome HSDN C0020672 Body temperature decreased C0011630 Dermatomycoses HSDN C0242936 Center pain C1705812 Nci thesaurus role HSDN C4084767 Bothered by vomiting C0033906 Psychological theories HSDN C4085210 Usual severity pain C0023281 Leishmaniasis HSDN C0151686 Growth retardation C0580190 3-phosphoglycerate dehydrogenase deficiency MalaCards C1963091 Diarrhea adverse event C1837028 Severe combined immunodeficiency, autosomal recessive, t cell negative, b cell positive, nk cell positive HPO C0000727 Abdomen acute C0020649 Hypotension HSDN C1145670 Failure respiratory C3280358 Wolfram-like syndrome, autosomal dominant MalaCards|HPO C2911645 Weight loss adverse event C0020255 Hydrocephalus HSDN C1963087 Constipation adverse event C0376547 Aromatherapy HSDN C2237041 Shox gene with short stature C0265220 Pallister-hall syndrome MalaCards|HPO C0427008 Stiffness C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|UMLS C2242578 Tongue dystonia C1414216 Dystonia 6, torsion (disorder) MalaCards|UMLS C0151311 Cranial nerve palsy C0334123 Histiocytosis, lipoid MalaCards C2315100 Pediatric failure to thrive C0154251 Lipid metabolism disorders HSDN C1963281 Vomiting adverse event C0020732 Iatrogenic disease HSDN C0043094 Weight gain C0009373 Colonic diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0039971 Thirst HSDN C1557397 Adverse event associated with pain C0206682 Follicular thyroid carcinoma HSDN C0018926 Emesis bloody C0022661 Kidney failure, chronic HSDN C1069915 Vertigo C0004275 Attitude health HSDN C0242936 Center pain C0000810 Incomplete spontaneous abortion HSDN C4085642 Level of joint stiffness C0015923 Fetal alcohol syndrome OrphaNet|MalaCards C0028738 Nystagmus C0796264 Young-hughes syndrome MalaCards C4085642 Level of joint stiffness C0037231 Sjogren-larsson syndrome MalaCards|HPO C1549543 Administration method - pain C0017536 Giardiasis HSDN C0002170 Alopecia disorders C1863094 Alopecia areata 1 MalaCards C0011991 Loose stools C1290807 Diarrheal disorder UMLS C2919142 Short stature adverse event C1833380 Velofacioskeletal syndrome OrphaNet|MalaCards C0557874 Global developmental delay C0432246 Microcephalic osteodysplastic primordial dwarfism, type ii HPO C1263846 Attention deficit disorder with hyperactivity C0035934 Rubinstein-taybi syndrome OrphaNet|MalaCards C0018989 Paresis of one side of body C0022336 Creutzfeldt-jakob disease MalaCards|HPO|UMLS C4084766 Vomiting C0162671 Melas syndrome HSDN C3898969 Have been vomiting C0151526 Premature birth HSDN C0917816 Deficiency mental C1260899 Anemia, diamond-blackfan HPO C2364082 Hyposmia C3889475 Bardet-biedl syndrome 19 MalaCards|UMLS C0033774 Skin pruritus C3543867 Collodion fetus MalaCards C0424755 Fever symptoms C0036986 Shock, traumatic HSDN C1557397 Adverse event associated with pain C0038017 Congenital spondylolisthesis HSDN C3641756 Have diarrhea C0019294 Hernia, inguinal HSDN C4085210 Usual severity pain C0036271 Scalp dermatoses HSDN C0028738 Nystagmus C1706192 Sulfatidosis MalaCards C0575081 Abnormal gait C3810289 Spastic paraplegia 64, autosomal recessive MalaCards C1963064 Anxiety adverse event C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C0349588 Stature short C1866927 Smcr HPO C0036396 Sciatica C0005967 Bone neoplasms HSDN C0016199 Pain flank C1333405 Eosinophilic variant of chromophobe renal cell carcinoma UMLS C4085210 Usual severity pain C0029184 Orbital fracture HSDN C0700590 Diaphoresis excessive C0014805 Primary erythermalgia MalaCards|HPO C0239134 Cough productive C0746158 Lung lll pneumonia UMLS C1962972 Proteinuria adverse event C0023470 Myeloid leukemia HSDN C2096293 Ent surgical result ear vertigo C1834580 Myoclonus and ataxia MalaCards C0522224 Palsied C0009373 Colonic diseases HSDN C0007758 Cerebellar ataxia C0037769 West syndrome HSDN C4084767 Bothered by vomiting C0206715 Neoplasms, neuroepithelial HSDN C1963087 Constipation adverse event C0162531 Hereditary coproporphyria OrphaNet|HPO C4084775 Usual severity weight loss C0032344 Poisoning aspects HSDN C4084767 Bothered by vomiting C0021361 Female infertility HSDN C3665347 Vision impaired C0022336 Creutzfeldt-jakob disease MalaCards|HPO C4085317 Diarrhea frequency C0149721 Left ventricular hypertrophy HSDN C4085210 Usual severity pain C0019294 Hernia, inguinal HSDN C0557874 Global developmental delay C0795939 Aminopterin syndrome sine aminopterin MalaCards C0023014 Developmental disorder language C0265354 Charge syndrome HSDN C0030193 Sense of pain C0008732 Chylous ascites HSDN C0344315 Mood depressed C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C1961131 Cough adverse event C0026650 Movement disorders HSDN C1962972 Proteinuria adverse event C0149649 Cholesterol embolism HSDN C0040822 D tremors C0003850 Arteriosclerosis HSDN C4042891 Sleep wake disorders C0020541 Hypertension, portal HSDN C0031911 Pigment deposition C0154893 Hereditary choroid dystr. nos MalaCards C0231528 Muscle pain generalized C0079218 Fibromatosis, aggressive OrphaNet|HPO|MalaCards C4085211 Pain distress question C0242596 Neoplasm, residual HSDN C3539890 Pelvic pain causes awakening at night C1550672 Specimen type - ulcer HSDN C0018772 Deafness C0041330 Tuberculosis, spinal HSDN C0151825 Ostalgia C0432282 Dysplasia epiphysealis hemimelica OrphaNet|MalaCards C0151786 Weakness muscle C1856403 Etfb deficiencies HPO C1963137 Hydrocephalus adverse event C3554657 Lissencephaly 5 MalaCards C0424755 Fever symptoms C0007130 Mucinous adenocarcinoma HSDN C0012833 Dizzy C0553860 Viral epidemic vertigo UMLS C0085650 Purpura fulminans C0158570 Vascular anomaly HSDN C3463815 Feel fatigue C0040053 Thrombosis HSDN C0518090 Frequency of pain question C0001622 Adrenal gland hyperfunction HSDN C0018681 Headache, cephalalgia C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0151825 Ostalgia C0024454 Maffucci syndrome OrphaNet|HPO|MalaCards C0009806 Constipate C0497327 Dementia HSDN C0039070 Collapse fleeting C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0018784 Deafness sensorineural C0585442 Osteosarcoma of bone HSDN C0024031 Back pain lower back C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C1963071 Back pain adverse event C0042830 Perception visual HSDN C4084773 Bothered by weight gain C0042134 Uterine hemorrhage HSDN C0241210 Speaking delay C3279839 Mental retardation, autosomal dominant 7 MalaCards C4084768 Usual severity vomiting C0033968 Psychotherapeutic technique HSDN C2984057 Have nausea C0162576 Anisakiasis MalaCards C0007758 Cerebellar ataxia C0013808 Electroconvulsive therapy HSDN C4084769 Vomiting frequency C0005416 Biliary dyskinesia HSDN C4084776 Weight loss C0039971 Thirst HSDN C0033377 Caudal displacement C3810285 Myopathy with extrapyramidal signs MalaCards C0042963 Symptoms vomiting C0020676 Hypothyroidism HSDN C3541349 Syncope C0024141 Lupus erythematosus, systemic HSDN C0018784 Deafness sensorineural C0027439 Nasopharyngeal neoplasms HSDN C2203646 Jaundice C0024437 Macular degeneration HSDN C1549543 Administration method - pain C0013291 Duodenal neoplasms HSDN C0013395 Indigestion C0034194 Pyloric stenosis HSDN C1384666 Decreased hearing C0024530 Malaria HSDN C0851578 Disorder sleep C0018802 Congestive heart failure HSDN C3898969 Have been vomiting C2931187 Nephropathic cystinosis MalaCards C0349588 Stature short C0796068 Oculodigitoesophagoduodenal syndrome OrphaNet C0022346 Yellow skin C0037397 Behavior social HSDN C4084773 Bothered by weight gain C0004626 Pneumonia, bacterial HSDN C0018772 Deafness C0265289 Metaphyseal chondrodysplasia schmid type OrphaNet|HPO|MalaCards C1963063 Anorexia adverse event C0268581 Holocarboxylase synthetase deficiency OrphaNet|HPO|MalaCards C3887784 Decreased urine output C0085083 Ovarian hyperstimulation syndrome HSDN C0015672 Decreased energy C0040558 Toxoplasmosis HSDN C0006370 Bulimia C1706377 Memory device component HSDN C4084776 Weight loss C0947622 Cholecystolithiasis HSDN C0000737 Abdomen pain C0524620 Metabolic syndrome x HSDN C3815497 Cough C0018200 Granuloma, respiratory tract HSDN C0002962 Angina C1548578 Location characteristic id - smoking HSDN C2096293 Ent surgical result ear vertigo C3887678 Cpnet MalaCards C0151786 Weakness muscle C0268573 Valinemia MalaCards C0010520 Skin cyanosis C0025202 Melanoma HSDN C0042571 Vertigo subjective C0997768 Glaucoma HSDN C0020672 Body temperature decreased C0014457 Eosinophilia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0009088 Cluster headache HSDN C0033074 Presbycusis C3160736 Deafness, autosomal dominant 51 MalaCards C0009792 Consciousness disorder C1145670 Respiratory failure HSDN C0007859 Pain neck C2984289 Melanoma pathway HSDN C4085211 Pain distress question C0020635 Hypopituitarism HSDN C2024893 Cardiovascular surgery result: fatigue C0018939 Hematological disease HSDN C4084769 Vomiting frequency C0007193 Cardiomyopathy, dilated HSDN C0012569 Double vision C0024299 Lymphoma HSDN C1963063 Anorexia adverse event C0154246 Urea cycle disorders, inborn HSDN C0000737 Abdomen pain C3826981 Md-ipmn UMLS C1384666 Decreased hearing C0010823 Cytomegalovirus infections HSDN C1963252 Tremor adverse event C2930900 Beta-sarcoglycanopathy MalaCards C0020458 Hyperhydrosis C1302282 Chromaffin cell neoplasm MalaCards C0027497 Queasy C0019693 Hiv infections HSDN C4084727 Cough frequency C0027819 Neuroblastoma HSDN C1384666 Decreased hearing C1832845 Usher syndrome, type id HPO C4084769 Vomiting frequency C0011616 Contact dermatitis HSDN C0026821 Cramp C0024003 Lordosis HSDN C0007859 Pain neck C0018790 Cardiac arrest HSDN C1557397 Adverse event associated with pain C1959600 Obscure african cardiomyopathy HSDN C1557397 Adverse event associated with pain C0030920 Peptic ulcer HSDN C1961131 Cough adverse event C0024899 Mastocytosis MalaCards C0036572 Convulsion C1850056 Peho-like syndrome HPO C0016204 Fart C0007001 Carbohydrate metabolism, inborn errors HSDN C2032396 Pelvic pain on the right C0032966 Complication, neoplastic pregnancy HSDN C1384666 Decreased hearing C0004935 Animal ethology HSDN C4085317 Diarrhea frequency C1527429 Increased blood npn HSDN C2919142 Short stature adverse event C0265265 Aase syndrome MalaCards|HPO C4085317 Diarrhea frequency C0175816 Cold hemagglutinin disease MalaCards C0522224 Palsied C3179088 Injuries, lingual nerve HSDN C0000737 Abdomen pain C0334277 Adenocarcinoma, metastatic UMLS C0043094 Weight gain C1522137 Hypertriglyceridemia result HSDN C0030554 Abnormal sensation C0014511 Epithelial cyst HSDN C3898969 Have been vomiting C0003855 Arteriovenous fistula HSDN C4084776 Weight loss C0035066 Renal artery obstruction HSDN C0010520 Skin cyanosis C1546635 Specimen source codes - fistula HSDN C0000731 Abdomen distention C0265344 Donohue syndrome HPO C4085222 Nausea C0162565 Acute intermittent porphyria MalaCards|HPO C0042024 Urine incontinence C0019294 Hernia, inguinal HSDN C3641756 Have diarrhea C0025267 Multiple endocrine neoplasia type 1 OrphaNet|HPO C1549543 Administration method - pain C0007095 Carcinoid tumor HSDN C0150055 Pain chronic C0302148 Blood clot HSDN C0003862 Pain joint C0027095 Myosarcoma HSDN C1963184 Nystagmus adverse event C0078918 Albinism, oculocutaneous OrphaNet C0234512 Prosopagnosia C0002395 Alzheimer's disease HSDN C2024893 Cardiovascular surgery result: fatigue C0036916 Sexually transmitted diseases HSDN C3887873 Hearing loss C0042075 Urologic diseases HSDN C0242936 Center pain C0242188 Spider bites HSDN C0522224 Palsied C0006261 Bronchial diseases HSDN C4084775 Usual severity weight loss C0004030 Aspergillosis HSDN C0424755 Fever symptoms C0018572 Hand, foot and mouth disease DiseaseOntology|HSDN|MalaCards C1549543 Administration method - pain C0040820 Trematode infections HSDN C0003467 Angst C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C0917801 Sleep disorder insomnia C1561841 Adjustment insomnia UMLS C3887638 Failure to thrive in infant C0151467 Addisonian crisis OrphaNet|MalaCards C0497406 Over weight C1457883 Aggressive reaction HSDN C1963065 Apnea adverse event C0026769 Multiple sclerosis HSDN C1557397 Adverse event associated with pain C0085110 Severe combined immunodeficiency HSDN C0009792 Consciousness disorder C0023903 Liver neoplasms HSDN C0027066 Myoclonic jerking C0026848 Myopathy HSDN|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0549567 Pigmentation disorders HSDN C0917816 Deficiency mental C1833691 Otofaciocervical syndrome OrphaNet|HPO C4084774 Have weight loss C0021280 Infant nutrition disorder HSDN C0019572 Hairiness C0270972 Cornelia de lange syndrome HPO C0019209 Large liver C0311298 Propionic acidemia, type ii OrphaNet|HPO C0497247 Blood pressure elevation C1862170 Brachydactyly with hypertension OrphaNet|HPO|MalaCards C0231712 Gait waddling C1850792 Congenital myasthenic syndrome ib MalaCards|HPO C3274924 Have been coughing C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C4084725 Usual severity cough C1963138 Hypertension adverse event HSDN C0427009 Joint stiffness nec C0427023 Stiff mcp joint nec UMLS C0001707 Aerophagia C3827868 Tachycardia by ecg finding HSDN C0018834 Brash C0279628 Adenocarcinoma of esophagus OrphaNet C0034124 Pupillary disorder C0004106 Astigmatism HSDN C0851578 Disorder sleep C0205788 Histiocytoid hemangioma HSDN C0019572 Hairiness C0013080 Down syndrome HSDN C0242936 Center pain C0305062 Tetanus toxoids HSDN C1963091 Diarrhea adverse event C0026640 Mouth neoplasms HSDN C0018784 Deafness sensorineural C0027663 Neoplasms, multiple primary HSDN C2984057 Have nausea C0812393 Cancer patients and suicide and depression HSDN C0033377 Caudal displacement C4014660 Combined oxidative phosphorylation deficiency 20 MalaCards C0024031 Back pain lower back C0001973 Alcoholic intoxication, chronic HSDN C2203646 Jaundice C0000817 Abortion septic HSDN C1963091 Diarrhea adverse event C0013289 Duodenal diseases HSDN C0030486 Extremity paralysis, lower C0702166 Acne HSDN C0232466 Feeding difficulty C0341106 Eosinophilic esophagitis MalaCards C0039231 Heartbeats increased C0162565 Acute intermittent porphyria MalaCards|HPO C1962972 Proteinuria adverse event C0001824 Agranulocytosis HSDN C4084769 Vomiting frequency C0020437 Hypercalcemia HSDN C4084784 Diarrhea C0011974 Diaper rash HSDN C4084724 Usual severity constipation C0033578 Prostatic neoplasms HSDN C2126054 Rectal sore with bleeding C0267596 Bleeding rectal UMLS C0039070 Collapse fleeting C0005967 Bone neoplasms HSDN C0012569 Double vision C0026764 Multiple myeloma HSDN C0344315 Mood depressed C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards C4084897 Sleep disturbance subordinate domain C2931878 Familial primary biliary cirrhosis MalaCards C0235299 Abdomen ruq pain C0023895 Liver diseases UMLS C4042891 Sleep wake disorders C0024530 Malaria HSDN C0009421 Comatose C0014053 Encephalitis, california DiseaseOntology|MalaCards C3665492 Pigmentations C0007965 Chediak-higashi syndrome MalaCards C2237041 Shox gene with short stature C0393559 Troyer syndrome HPO C0002962 Angina C0035410 Rhabdomyolysis HSDN C0040034 Thrombocytopenia C1327918 Oculootoradial syndrome MalaCards|HPO C4084766 Vomiting C0030353 Papilledema HSDN C0522224 Palsied C0013274 Patent ductus arteriosus HSDN C0002962 Angina C0004943 Behcet syndrome HSDN C0024031 Back pain lower back C3539923 Cdisc adas-cog - orientation summary score HSDN C4084784 Diarrhea C0042995 Vulvar neoplasms HSDN C0015672 Decreased energy C0019542 Higher nervous activity HSDN C0242936 Center pain C0085435 Arthritis, reactive MalaCards|HSDN C0019521 Hiccoughs C0751873 Demyelinating autoimmune diseases, cns HSDN C0000737 Abdomen pain C1514199 Ovarian polyembryoma UMLS C0011991 Loose stools C0030793 Pelvis tumor HSDN C0020455 Hypergammaglobulinemia C0019625 Sinus histiocytosis HSDN C1145670 Failure respiratory C0004031 Aspergillosis, allergic bronchopulmonary MalaCards C3541349 Syncope C0014859 Esophageal neoplasms HSDN C0557874 Global developmental delay C0795830 Chromosome 9p deletion syndrome OrphaNet|MalaCards C3274924 Have been coughing C0524851 Neurodegenerative disorders HSDN C0018991 Paralysis one side of body C0000771 Abnormalities, drug induced HSDN C0023380 Lethargy C0010399 Crying HSDN C2919142 Short stature adverse event C3151302 Chromosome 13q14 deletion syndrome MalaCards C0349588 Stature short C0342488 Mineralocorticoid excess syndrome, apparent MalaCards C0034915 Redness or discharge of eye C0497217 Other disease of eye UMLS C2919142 Short stature adverse event C1442965 Avascular necrosis of the capital femoral epiphysis MalaCards C3827868 Tachycardia by ecg finding C0334419 Pheochromocytoma, malignant MalaCards C2919142 Short stature adverse event C0265376 Fetal methyl mercury syndrome OrphaNet C1836296 Lower extremity weakness C0035410 Rhabdomyolysis MalaCards C0271215 Blindness legal C0266526 Norrie disease OrphaNet|HPO|MalaCards C3641755 Have constipation C0162871 Aortic aneurysm, abdominal HSDN C0007758 Cerebellar ataxia C0795889 Allan-herndon-dudley syndrome (ahds) OrphaNet|HPO|MalaCards C4084788 Have dizziness C0024299 Lymphoma HSDN C4084767 Bothered by vomiting C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C3815497 Cough C0702166 Acne HSDN C0026821 Cramp C1855849 Bartter syndrome, antenatal , type 2 HPO|UMLS C0018991 Paralysis one side of body C1963064 Anxiety adverse event HSDN C0575081 Abnormal gait C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0727671 Red cross toothache drops C0040149 Subacute thyroiditis HSDN C0242936 Center pain C0015459 Face injury HSDN C0030554 Abnormal sensation C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0024031 Back pain lower back C0027794 Neural tube defects HSDN C2911647 Weight gain adverse event C0162526 Aids-related opportunistic infections HSDN C1963281 Vomiting adverse event C0241158 Cicatrix skin HSDN C0349588 Stature short C1527404 Female pseudo-turner syndrome HPO C4085211 Pain distress question C0019337 Heroin dependence HSDN C0004093 Asthenia C0019209 Hepatomegaly HSDN C1384666 Decreased hearing C0023092 Lassa fever MalaCards C1963071 Back pain adverse event C2186740 Reported urticaria HSDN C1836296 Lower extremity weakness C0007137 Squamous cell carcinoma UMLS C4085549 Dizziness C0008066 Child behavior disorders HSDN C0026858 Musculoskeletal pain C1532253 Sedentary lifestyle HSDN C0522224 Palsied C2073625 X-ray of chest: pleural effusion HSDN C0026205 Pupillary constriction C0034951 Refractive errors HSDN C0009460 Communication impairment C0236964 Attention deficit and disruptive behavior disorders HSDN C3146279 Coma C0013473 Eating disorders HSDN C0037317 Sleep disturbance C2675336 Duplication 15q11-q13 syndrome MalaCards C3887638 Failure to thrive in infant C3152144 Agammaglobulinemia 1, autosomal recessive HPO C4084775 Usual severity weight loss C0015927 Intrauterine fetal demise HSDN C4085211 Pain distress question C0007860 Uterine cervicitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0037019 Shy-drager syndrome HSDN C3898969 Have been vomiting C0006663 Calcinosis HSDN C4085210 Usual severity pain C0001857 Aids related complex HSDN C0011175 Deficient fluid volume C2749685 Cystinosis, atypical nephropathic (disorder) HPO C0232209 Contractions junctional premature C0340464 Heartbeats ectopic UMLS C1963063 Anorexia adverse event C0854176 Malignant hepato-biliary neoplasm MalaCards C0018834 Brash C0027651 Tumor HSDN C2911645 Weight loss adverse event C0005424 Biliary tract diseases HSDN C0004941 Behavioral symptoms C0043379 Xyy karyotype OrphaNet C0031911 Pigment deposition C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0241137 Skin pallor C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C0030552 Paralysis partial C0030286 Pancreatic diseases HSDN C0041105 Jaw spasm C0026650 Movement disorders HSDN C0035232 Diaphragmatic paralysis C0039984 Thoracic outlet syndrome HSDN C0015672 Decreased energy C0027626 Neoplasm invasiveness HSDN C2203646 Jaundice C1690964 Cataract HSDN C4084776 Weight loss C1963148 Iron overload adverse event HSDN C0424755 Fever symptoms C0004659 Bacteriuria HSDN C0027066 Myoclonic jerking C0000735 Abdominal neoplasms HSDN C0751295 Memory loss or impairment C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C0184567 Pain acute C0042487 Venous thrombosis HSDN C3898969 Have been vomiting C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C0151786 Weakness muscle C0023903 Liver neoplasms HSDN C0917816 Deficiency mental C3806917 Craniosynostosis 4 MalaCards C0015970 Fever unknown origin C0013902 Elliptocytosis, hereditary HSDN C3641756 Have diarrhea C0020876 Ileal neoplasms HSDN C0162298 Stiffness joints C1835084 Megaduodenum and-or megacystis MalaCards|HPO C0746674 Muscle weakness generalized C4225405 Myasthenic syndrome, congenital, 1b, fast-channel UMLS C4020887 Photodysphoria C2931280 Congenital alopecia, psychomotor retardation, convulsions OrphaNet|HPO|MalaCards C0027066 Myoclonic jerking C0087012 Ataxia, spinocerebellar HSDN C0040822 D tremors C0205711 Pelizaeus-merzbacher disease MalaCards|HPO C0398650 Idiopathic thrombocytopenia purpura C0494491 Mononeuropathies HSDN C0019825 Voice hoarseness C0006849 Oral candidiasis HSDN|UMLS C1384666 Decreased hearing C0406704 Rudiger syndrome 1 MalaCards C1963071 Back pain adverse event C0017601 Glaucomas HSDN C0518090 Frequency of pain question C0000810 Incomplete spontaneous abortion HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011608 Dermatitis herpetiformis HSDN C0349588 Stature short C0268335 Ehlers-danlos syndrome type 1 HPO C0030193 Sense of pain C0015328 Behavior, exploratory HSDN C0151315 Neck rigid C0001175 Acquired immunodeficiency syndrome UMLS C4084766 Vomiting C1963198 Pancreatitis adverse event HSDN C0018784 Deafness sensorineural C0010674 Cystic fibrosis HSDN C0015468 Face pain C0016735 Frontal sinusitis HSDN C1384666 Decreased hearing C0162671 Melas syndrome HSDN C0522224 Palsied C0243026 Sepsis HSDN C4085549 Dizziness C0018939 Hematological disease HSDN C0008031 Pain chest C0559260 Congenital scoliosis HSDN C2237041 Shox gene with short stature C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0019079 Bloody sputum C0854985 Adenocarcinoma of lung, stage i UMLS C0036572 Convulsion C2931008 Congenital disorder of glycosylation type 2a MalaCards|HPO|UMLS C1959630 Eye pain adverse event C0033817 Pseudomonas infections HSDN C1963184 Nystagmus adverse event C0265249 Mietens' syndrome MalaCards C1963071 Back pain adverse event C1962983 Cataract adverse event HSDN C0018772 Deafness C2676285 Bone fragility with contractures, arterial rupture, and deafness HPO C4084776 Weight loss C0031345 Pharyngeal diseases HSDN C3146279 Coma C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0037384 Snore C2984299 Asthma pathway HSDN C4085317 Diarrhea frequency C1565489 Renal insufficiency HSDN C2700617 Irritation - emotion C0265498 48, xxxy syndrome MalaCards C0011124 Libido decreased C2063827 Male hypoactive sexual desire due to physical condition UMLS C0151686 Growth retardation C1838657 Vitamin d hydroxylation-deficient rickets, type 1b HPO C0011168 Disorder deglutition C3537440 Cystinosis, infantile nephropathic MalaCards C0557874 Global developmental delay C2677109 Leukodystrophy, hypomyelinating, 4 MalaCards|HPO C0018681 Headache, cephalalgia C3899644 Childhood protoplasmic astrocytoma UMLS C0002962 Angina C1739395 Takotsubo cardiomyopathy HSDN C0027498 Nausea vomiting C3489856 Cold hypersensitivity MalaCards C1963087 Constipation adverse event C1145670 Respiratory failure HSDN C4084802 Usual severity diarrhea C0002170 Alopecia HSDN C1549543 Administration method - pain C0015732 Fecal incontinence HSDN C0040264 Ear ringing sound C0029401 Osteitis deformans HSDN C2984058 Have pain C0001627 Congenital adrenal hyperplasia HSDN C3641756 Have diarrhea C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0012644 Animal disease models HSDN C2984058 Have pain C0392622 Toxic effect of carbon tetrachloride HSDN C0426579 Anorexia symptom C0010709 Cyst HSDN C4085661 Usual severity nausea C0241158 Cicatrix skin HSDN C4084724 Usual severity constipation C0036202 Sarcoidosis HSDN C0018681 Headache, cephalalgia C0003463 Anus neoplasms HSDN C2096293 Ent surgical result ear vertigo C0023267 Fibroid tumor HSDN C0042571 Vertigo subjective C0062527 Hepatitis b vaccine HSDN C0917816 Deficiency mental C0342194 Thyroid dyshormonogenesis 3 MalaCards|HPO C0011991 Loose stools C0036262 Sarcoptic itch HSDN C1999266 Depression adverse event C0010308 Congenital hypothyroidism OrphaNet C0034150 Skin purpura C0085278 Antiphospholipid syndrome HSDN C4085210 Usual severity pain C0008412 Choline deficiency HSDN C0234132 Pyramidal sign C1850100 Parkinson disease 15, autosomal recessive (disorder) UMLS C0427055 Face weakness C0265234 Branchio-oto-renal syndrome MalaCards|HPO C0026821 Cramp C3552335 Myasthenic syndrome, congenital, 12 UMLS C0018681 Headache, cephalalgia C0022658 Kidney diseases HSDN C0042963 Symptoms vomiting C0015732 Fecal incontinence HSDN C0020903 Illusion C0037274 Dermatologic disorders HSDN C2875629 Eyelid retraction left eye, unspecified eyelid C0497217 Other disease of eye UMLS C0036572 Convulsion C0019557 Hip fx HSDN C0004134 Dyssynergia C0027773 Nesidioblastosis HSDN C0039070 Collapse fleeting C0700327 Clinical findings relating to memory HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023801 Lipomatosis HSDN C0030552 Paralysis partial C3887992 Thyrotropin-releasing hormone deficiency MalaCards C4084723 Constipation C2073625 X-ray of chest: pleural effusion HSDN C0009806 Constipate C0007570 Celiac disease DiseaseOntology|HSDN C2024878 Cardiovascular surgery result: dyspnea C0221348 Hereditary lymphedema and yellow nails OrphaNet|MalaCards C0030552 Paralysis partial C0262593 Injury nerve peripheral HSDN C2911647 Weight gain adverse event C0362046 Prediabetes syndrome HSDN C0151786 Weakness muscle C1962979 Burn adverse event HSDN C3665347 Vision impaired C3150691 Retinitis pigmentosa 54 MalaCards|HPO C0349489 Fetal hypoxia C0007020 Carbon monoxide poisoning HSDN C3539891 Pelvic pain to the rear C0042341 Varicocele HSDN C0424755 Fever symptoms C0018817 Atrial septal defects HSDN C1962972 Proteinuria adverse event C0026918 Mycobacterium infections HSDN C1579931 Depressed - symptom C3280358 Wolfram-like syndrome, autosomal dominant OrphaNet|HPO|MalaCards C0035078 Failure kidney C0037054 Sickle cell trait MalaCards C0018784 Deafness sensorineural C0752160 Hemangioma, cavernous, central nervous system HSDN C2132198 Abnormal blistering of the skin C3554246 Focal facial dermal dysplasia 4 MalaCards C1510417 Apraxia of gait C0393665 Multiple sclerosis, chronic progressive HSDN C0018808 Murmur C0037221 Situs inversus HSDN C0037763 Spasm C0238265 Encephalopathy, callosal demyelinating HSDN C0015469 Facial paralysis C1963198 Pancreatitis adverse event HSDN C0041667 Low weight C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C0542476 Forgetful C1846564 Spastic paraplegia 7, autosomal recessive MalaCards|HPO C2911645 Weight loss adverse event C0152018 Esophageal carcinoma OrphaNet|MalaCards C2919142 Short stature adverse event C3150890 Brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation MalaCards C0000727 Abdomen acute C0597109 Nurse's role HSDN C0184567 Pain acute C0032787 Postoperative complications HSDN C0231528 Muscle pain generalized C1846672 Muscular dystrophy, limb-girdle, type 2i MalaCards|HPO|UMLS C1557397 Adverse event associated with pain C0042594 Vestibular diseases HSDN C4084775 Usual severity weight loss C0003493 Aortic diseases HSDN C0043094 Weight gain C0242339 Dyslipidemias HSDN C0518090 Frequency of pain question C0011848 Diabetes insipidus HSDN C1963064 Anxiety adverse event C3494506 Pseudohypoparathyroidism, type ia HPO C3539889 Pelvic pain increasing in severity C0026769 Multiple sclerosis HSDN C0011991 Loose stools C0023220 Leg injury HSDN C4085211 Pain distress question C0085404 Poems syndrome MalaCards|HSDN C0042571 Vertigo subjective C0035435 Rheumatism HSDN C0012833 Dizzy C0338487 Benign paroxysmal vertigo of childhood UMLS C4085211 Pain distress question C0019202 Hepatolenticular degeneration HSDN C0018681 Headache, cephalalgia C0206743 Rhabdoid tumor OrphaNet|MalaCards C4084723 Constipation C0344490 Sacral agenesis HPO C1549543 Administration method - pain C0029001 Onchocerciasis HSDN C0019079 Bloody sputum C0025062 Mediastinal emphysema HSDN C4049602 Hyperactivity C2750791 Mental retardation, autosomal recessive 13 HPO C4084784 Diarrhea C1546654 Specimen source codes - granuloma HSDN C0015672 Decreased energy C0027663 Neoplasms, multiple primary HSDN C4085317 Diarrhea frequency C0011615 Dermatitis, atopic HSDN C0042755 Virilisation C0001144 Acne vulgaris HSDN C1963249 Tinnitus adverse event C2674004 Von hippel-lindau syndrome, modifiers of HPO C0013362 Dysarthrias C0751120 Benign infantile myoclonic epilepsy MalaCards C4085210 Usual severity pain C4042784 Feeding and eating disorders HSDN C0042024 Urine incontinence C0029408 Degenerative polyarthritis HSDN C1069915 Vertigo C0700501 Congenital nystagmus HSDN C2237041 Shox gene with short stature C3489726 Geleophysic dysplasia MalaCards C0518090 Frequency of pain question C0015456 Facial dermatoses HSDN C1963170 Hypothermia adverse event C0013928 Fat embolism HSDN C4084776 Weight loss C0221026 X-linked agammaglobulinemia HPO C3539895 Pelvic pain occurs with bowel movement C0042253 Vaginal fistula HSDN C0026821 Cramp C2932716 Pseudohypoparathyroidism type 1c HPO C4084784 Diarrhea C0037355 Smallpox vaccines HSDN C1546759 Specimen source codes - pustule C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome OrphaNet|MalaCards C0027497 Queasy C0023176 Lead poisoning HSDN C0020615 Hypoglycemia nos C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C1557397 Adverse event associated with pain C0005398 Cholestasis, extrahepatic HSDN C0233763 Hallucinations visual C0015397 Disorder of eye UMLS C0522224 Palsied C0000735 Abdominal neoplasms HSDN C0004604 Pain back C0220847 C hepatitis virus HSDN C1962972 Proteinuria adverse event C0027868 Neuromuscular diseases HSDN C2700617 Irritation - emotion C0268467 Hyperphenylalaninemia, bh4-deficient, b MalaCards|HPO C0036572 Convulsion C0238052 Xanthomatosis, cerebrotendinous MalaCards|HPO C0018772 Deafness C0027858 Neuroma HSDN C0020538 Hbp C1859570 Bardet-biedl syndrome 12 HPO C2030274 Heavy bleeding between periods C0025874 Metrorrhagia UMLS C0009080 Finger clubbing C0238386 Cronkhite-canada disease MalaCards C2024893 Cardiovascular surgery result: fatigue C0029456 Osteoporosis HSDN C0010200 Cough symptom C0008677 Bronchitis, chronic MalaCards|UMLS C0031911 Pigment deposition C0339527 Leber congenital amaurosis MalaCards C0033377 Caudal displacement C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C4084775 Usual severity weight loss C0085632 Apathy HSDN C4084767 Bothered by vomiting C0948039 Bacterial gastritis MalaCards C4085211 Pain distress question C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0020538 Hbp C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards C0042798 Vision dim C1852429 Cataract, variable zonular pulverulent MalaCards C4084767 Bothered by vomiting C0032285 Pneumonia HSDN C2911645 Weight loss adverse event C0085278 Antiphospholipid syndrome HSDN C1963063 Anorexia adverse event C0014868 Esophagitis HSDN C0022346 Yellow skin C0008350 Cholelithiasis MalaCards|HSDN|HPO|UMLS C0018834 Brash C0795833 Kleefstra syndrome HPO C0542476 Forgetful C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C4085862 Bothered by nausea C0030297 Pancreatic neoplasm HSDN C0030554 Abnormal sensation C1710146 Familial spinal arachnoiditis MalaCards C0018784 Deafness sensorineural C0007959 Charcot-marie-tooth disease HSDN C4084773 Bothered by weight gain C0014868 Esophagitis HSDN C4084784 Diarrhea C0005758 Bulla HSDN C1279888 Proteinuria of undiagnosed cause C0027126 Myotonic dystrophy HSDN C0037317 Sleep disturbance C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0002622 Amnesias C0036974 Shock HSDN C0019209 Large liver C1835912 Aicardi-goutieres syndrome 4 MalaCards|HPO C0019079 Bloody sputum C0854986 Lung adenocarcinoma stage ii UMLS C0042963 Symptoms vomiting C1855652 Fetus small for gestational age HSDN C0034933 Abnormal reflexes C0037769 West syndrome HSDN C1860844 Sparse, thin hair C1836123 Goldberg-shprintzen megacolon syndrome HPO C0349588 Stature short C0796021 Lowry wood syndrome OrphaNet|MalaCards C3539891 Pelvic pain to the rear C0010692 Cystitis HSDN C4084784 Diarrhea C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C4084784 Diarrhea C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C2984058 Have pain C0019114 Hemosiderosis HSDN C4085222 Nausea C0033975 Psychotic disorders HSDN C0413252 Hypothermia due to exposure C0034065 Pulmonary embolism HSDN C3539896 Pelvic pain occurs with urination C2586211 Thrombosis of blood vessel HSDN C1963071 Back pain adverse event C0037369 Smoking HSDN C0000737 Abdomen pain C0085413 Polycystic kidney, autosomal dominant HSDN C0518090 Frequency of pain question C1963235 Sick sinus syndrome adverse event HSDN C3539023 Pelvic pain increasing in frequency C0029436 Bone disease, disappearing HSDN C3641756 Have diarrhea C0034089 Pulmonary valve stenosis HSDN C0036659 Sensation disorder C0016989 Galvanic skin response HSDN C0010200 Cough symptom C0011265 Presenile dementia HSDN C1557397 Adverse event associated with pain C0162871 Aortic aneurysm, abdominal HSDN C4084725 Usual severity cough C1546949 Event consequence - death HSDN C0003079 Pupillary inequality C0020620 Hypohidrosis HSDN C0231218 Malaise generalized C1112459 Non-resectable hepatocellular carcinoma UMLS C1557397 Adverse event associated with pain C0019061 Hemolytic-uremic syndrome HSDN C0027796 Neuralgias C0029408 Degenerative polyarthritis HSDN C4084725 Usual severity cough C0014854 Esophageal diverticulum HSDN C3641755 Have constipation C0302148 Blood clot HSDN C1963137 Hydrocephalus adverse event C3554385 Congenital disorder of glycosylation, type iu MalaCards C1557397 Adverse event associated with pain C0018915 Hemangioendothelioma HSDN C4085317 Diarrhea frequency C0149678 Epstein-barr virus infections HSDN C1557397 Adverse event associated with pain C0030312 Pancytopenia HSDN C0020578 Hyperventilate C0036421 Systemic scleroderma HSDN C0917801 Sleep disorder insomnia C4237471 Unspecified insomnia disorder UMLS C3887638 Failure to thrive in infant C2931007 Congenital disorder of glycosylation type 1x MalaCards|HPO C0026838 Spasticity muscle C0014070 Encephalomyelitis HSDN C0037317 Sleep disturbance C0033138 Primary hypersomnia MalaCards C0030193 Sense of pain C0948089 Acute coronary syndrome HSDN C0018524 Hallucinate C0032285 Pneumonia HSDN C0030193 Sense of pain C0027719 Nephrosclerosis HSDN C0007642 Cellulitis nos C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0700590 Diaphoresis excessive C1851479 Keratoderma palmoplantaris transgrediens OrphaNet C0018681 Headache, cephalalgia C0014057 Japanese encephalitis DiseaseOntology|MalaCards C4085211 Pain distress question C0002950 Aneurysms inflammatory HSDN C0036572 Convulsion C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C4085548 Usual severity dizziness C0040997 Trigeminal neuralgia HSDN C0003862 Pain joint C0024228 Lymphatic diseases HSDN C0008031 Pain chest C0019099 Hemorrhagic fever, crimean MalaCards C2700617 Irritation - emotion C0036391 Schwartz-jampel syndrome MalaCards|HPO C1963170 Hypothermia adverse event C0812393 Cancer patients and suicide and depression HSDN C4084784 Diarrhea C2004491 Cicatrix HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013100 Dracontiasis HSDN C0018681 Headache, cephalalgia C0020540 Malignant hypertension HSDN|UMLS C0476211 Dysfunctions associated with sleep stages C0154565 Non-organic sleep disorder UMLS C0023530 Leukopenia C0272170 Shwachman syndrome OrphaNet|HPO C4084725 Usual severity cough C0025007 Measles DiseaseOntology|HSDN|MalaCards C3665346 Loss sight C1858677 Leber congenital amaurosis 3 (disorder) MalaCards|HPO C0023012 Delay language C0268543 Hyperammonemia, type iii MalaCards C2029884 Hearing loss by exam C0023974 Loneliness HSDN C1963091 Diarrhea adverse event C0038395 Streptococcal infections HSDN C0018772 Deafness C0014848 Esophageal achalasia HSDN C0040034 Thrombocytopenia C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO C3829611 Nausea frequency C0008049 Chicken pox DiseaseOntology|HSDN|MalaCards C0042571 Vertigo subjective C0032285 Pneumonia HSDN C4084766 Vomiting C3812171 Bradycardia by ecg finding HSDN C0518090 Frequency of pain question C0085396 Neisseriaceae infections HSDN C4085862 Bothered by nausea C0032227 Pleural effusion disorder HSDN C0015970 Fever unknown origin C0040558 Toxoplasmosis HSDN C4084784 Diarrhea C0023241 Legionnaires' disease MalaCards C0727671 Red cross toothache drops C0694536 Drug-seeking behavior HSDN C0152020 Atony stomach C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0232466 Feeding difficulty C0555206 Chiari malformation type ii MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0020473 Hyperlipidemia HSDN C3641756 Have diarrhea C0346407 Pancreatic polypeptide-oma MalaCards C0151786 Weakness muscle C1834567 Myoglobinuria, autosomal dominant MalaCards C3641756 Have diarrhea C0042781 Visceral myopathy MalaCards C0085631 Abnormal excitement C0035243 Respiratory tract infections HSDN C0036572 Convulsion C2939465 Deficiency of glucose-6-phosphate dehydrogenase HSDN C2911647 Weight gain adverse event C0028758 Bonding HSDN C0007859 Pain neck C0282333 Relaxation therapies HSDN C0019209 Large liver C1866121 Autoimmune lymphoproliferative syndrome, type i, autosomal recessive HPO C1963249 Tinnitus adverse event C0206638 Giant cell tumor of bone HSDN C0036572 Convulsion C0206727 Nerve sheath tumors HSDN C2919142 Short stature adverse event C0398794 Hypopigmentation-immunodeficiency disease MalaCards C1549543 Administration method - pain C0085648 Synovial cyst HSDN C0034063 Edema lung C0020192 Hyaline membrane disease MalaCards C0460137 Push down or depress C0566602 Primary sclerosing cholangitis MalaCards|HPO C0030193 Sense of pain C1334807 Mucinous carcinoma of breast UMLS C1069915 Vertigo C0013364 Dysautonomia, familial HSDN C4084774 Have weight loss C0585442 Osteosarcoma of bone HSDN C0241210 Speaking delay C1968550 Mental retardation, x-linked, syndromic 13 MalaCards|HPO C0018681 Headache, cephalalgia C0268394 Hereditary cerebral amyloid angiopathy, dutch type OrphaNet|HPO C0013604 Edematous C0014378 Enterovirus infections HSDN C0040034 Thrombocytopenia C0019097 Hemorrhagic fever, argentinian MalaCards C0036572 Convulsion C0232488 Abdominal colic HSDN C0009676 Confusion state C0517960 Neurological status: consciousness HSDN C1384666 Decreased hearing C0599973 Waardenburg anophthalmia syndrome OrphaNet|HPO|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0040028 Thrombocythemia, essential OrphaNet|HPO|MalaCards C0151889 Reflexes tendon increased C0282525 Adrenoleukodystrophy, neonatal OrphaNet|HPO|MalaCards C4049602 Hyperactivity C0175691 Dubowitz syndrome MalaCards C3665346 Loss sight C3179239 Osteopetrosis autosomal dominant type 2 MalaCards C3539890 Pelvic pain causes awakening at night C0037072 Diseases sigmoid HSDN C0033774 Skin pruritus C0263345 Urticaria pigmentosa, diffuse erythrodermic type UMLS C4085210 Usual severity pain C0030482 Paraepithymia HSDN C3539891 Pelvic pain to the rear C0018799 Heart diseases HSDN C0026826 High muscle tone C0752308 Hypoxia-ischemia, brain HSDN C0857305 Thrombocytopenia purpura C0031154 Peritonitis HSDN C0018784 Deafness sensorineural C0006434 Burn injury HSDN C1000483 Genus anemia C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C3539895 Pelvic pain occurs with bowel movement C0030455 Parametritis HSDN C0413252 Hypothermia due to exposure C0344315 Depressed mood HSDN C0015468 Face pain C0040053 Thrombosis HSDN C0013362 Dysarthrias C0752140 Intracranial embolism HSDN C0557874 Global developmental delay C0268548 Hyperargininemia OrphaNet|HPO|MalaCards C0034933 Abnormal reflexes C0877172 Hematoma, epidural, spinal HSDN C0043094 Weight gain C0024143 Lupus nephritis HSDN C0242936 Center pain C0020435 Hyperbilirubinemia, hereditary HSDN C2919142 Short stature adverse event C1859519 Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification MalaCards C0018772 Deafness C0035304 Retinal degeneration HSDN C1963071 Back pain adverse event C0019294 Hernia, inguinal HSDN C0015672 Decreased energy C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0033774 Skin pruritus C0343115 Skin mastocytoma OrphaNet|HSDN|HPO|MalaCards C1963252 Tremor adverse event C0031117 Peripheral neuropathy HSDN C0011206 Delirium acute C0003873 Rheumatoid arthritis HSDN C0424755 Fever symptoms C0242231 Coronary stenosis HSDN C0030552 Paralysis partial C0022744 Knee injury HSDN C0018772 Deafness C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C3714552 Strength decreased C0917713 Becker muscular dystrophy UMLS C0030486 Extremity paralysis, lower C0027659 Neoplasms, experimental HSDN C3898969 Have been vomiting C1704972 Genomic orientation HSDN C0007758 Cerebellar ataxia C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C0036659 Sensation disorder C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1279888 Proteinuria of undiagnosed cause C0006384 Bundle-branch block HSDN C1546759 Specimen source codes - pustule C0035012 Reiter syndrome OrphaNet|MalaCards C2911645 Weight loss adverse event C0235974 Pancreatic carcinoma MalaCards C2029967 Heartburn related to exercise C0796197 Pashayan-pruzansky syndrome MalaCards C0018772 Deafness C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards C0015469 Facial paralysis C0003507 Aortic valve stenosis HSDN C4084776 Weight loss C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C4085317 Diarrhea frequency C0268187 Alpha, alpha-trehalase deficiency MalaCards|HPO C4084802 Usual severity diarrhea C0034013 Precocious puberty HSDN C0031911 Pigment deposition C0009761 Conjunctival neoplasms MalaCards C4085211 Pain distress question C0034628 Radius fracture HSDN C0567522 Nipple discharge - pus C0009450 Disease caused by microorganism UMLS C4084725 Usual severity cough C0011616 Contact dermatitis HSDN C3463815 Feel fatigue C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C2984058 Have pain C0000880 Acanthamoeba keratitis HSDN C0575081 Abnormal gait C1850168 Bruck syndrome 1 MalaCards C0241210 Speaking delay C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C1963252 Tremor adverse event C3827868 Tachycardia by ecg finding HSDN C0012569 Double vision C1306794 Wound botulism OrphaNet|MalaCards C4084776 Weight loss C0334489 Pancreatoblastoma OrphaNet|MalaCards C1963077 Bone pain adverse event C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0036572 Convulsion C0679360 Foodborne disease HSDN C0917816 Deficiency mental C1865285 Megalencephaly cutis marmorata telangiectatica congenita OrphaNet|HPO C4085862 Bothered by nausea C0003467 Anxiety HSDN C0026838 Spasticity muscle C0022661 Kidney failure, chronic HSDN C4085317 Diarrhea frequency C0035258 Restless legs syndrome HSDN C0013604 Edematous C0007762 Cerebellar neoplasms HSDN C0007758 Cerebellar ataxia C1412747 Bbs2 gene HPO C0018772 Deafness C0027902 Neuropsychological diagnosis HSDN C0015672 Decreased energy C1848561 Methylmalonic acidemia with homocystinuria OrphaNet|MalaCards C0231835 Respiration rate increased C0035220 Respiratory distress syndrome, newborn MalaCards C0030193 Sense of pain C0025239 Melorheostosis HSDN C0022346 Yellow skin C0011854 Diabetes mellitus, insulin-dependent HSDN C0009806 Constipate C0029456 Osteoporosis HSDN C0494475 Seizure generalized tonic clonic C0751785 Unverricht-lundborg syndrome HPO C0018834 Brash C0158683 Polycystic liver disease MalaCards|HPO C0018772 Deafness C1969645 Ataxia, spastic, 3, autosomal recessive MalaCards|HPO C0002170 Alopecia disorders C0282102 Chondrodysplasia punctata, x-linked dominant type HPO C4084776 Weight loss C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C0032617 High urine output C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0030193 Sense of pain C0013117 Dreaming HSDN C2203646 Jaundice C0012644 Animal disease models HSDN C1145670 Failure respiratory C1868684 Ear, patella, short stature syndrome MalaCards C2032396 Pelvic pain on the right C0029456 Osteoporosis HSDN C0018681 Headache, cephalalgia C0027809 Neurilemmoma HSDN C1557397 Adverse event associated with pain C0334082 Nevus, epidermal (disorder) OrphaNet C0857305 Thrombocytopenia purpura C0003811 Cardiac arrhythmia HSDN C0349588 Stature short C2931294 Wiedemann grosse dibbern syndrome MalaCards C0018772 Deafness C0206307 Canavan disease OrphaNet|HPO|MalaCards C0426576 Gastrointestinal symptom C0152167 Anal spasms UMLS C0020673 Hypothermia (central) (local) C1963164 Lymphopenia adverse event HSDN C0000737 Abdomen pain C0027868 Neuromuscular diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C0006057 Botulisms HSDN C3494358 Characteristic, prodromal C1458155 Mammary neoplasms HSDN C0010200 Cough symptom C1963083 Cholecystitis adverse event HSDN C4085549 Dizziness C0004935 Animal ethology HSDN C0020673 Hypothermia (central) (local) C0011630 Dermatomycoses HSDN C4084773 Bothered by weight gain C0086543 Cataract nos HSDN C0020578 Hyperventilate C0085417 Epilepsy, complex partial HSDN C0271215 Blindness legal C1848922 Hexosaminidase alpha-subunit deficiency (variant b) OrphaNet|MalaCards C0003862 Pain joint C0020550 Hyperthyroidism HSDN C0003079 Pupillary inequality C0003081 Anisometropia HSDN C0015672 Decreased energy C0080040 Polio post syndrome MalaCards C4042891 Sleep wake disorders C0006147 Breast fed HSDN C4084723 Constipation C0033975 Psychotic disorders HSDN C0000737 Abdomen pain C3273102 Gallbladder cystadenocarcinoma UMLS C2315100 Pediatric failure to thrive C1842563 Heterotopia, periventricular, autosomal recessive HPO C0015672 Decreased energy C0037397 Behavior social HSDN C0242936 Center pain C0008698 Maxillary sinusitis chronic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036216 Sarcoma, experimental HSDN C0917816 Deficiency mental C1257806 Chromosomal instability MalaCards C0413252 Hypothermia due to exposure C1962958 Hematoma adverse event HSDN C0150045 Urinary incontinence urge C0010692 Cystitis HSDN C0003862 Pain joint C0276289 Zika virus infection MalaCards C4085317 Diarrhea frequency C4014233 Immunodeficiency 22 MalaCards C1384666 Decreased hearing C1846421 Lathosterolosis OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1868081 Juvenile polyposis coli HPO C0030193 Sense of pain C1333443 Esophageal basaloid carcinoma UMLS C0022346 Yellow skin C0003467 Anxiety HSDN C2315100 Pediatric failure to thrive C3276276 Mitochondrial complex v (atp synthase) deficiency, nuclear type 1 MalaCards C0152227 Tearing excessive C1274795 Urban schosser spohn syndrome MalaCards C0015230 Exanthem C0014740 Erythema chronicum migrans UMLS C0018681 Headache, cephalalgia C0019034 Hemoglobin sc disease UMLS C0162834 Hyperpigmentation C0162530 Porphyria, erythropoietic HPO C0018808 Murmur C0036400 Scimitar syndrome HSDN C0009398 Color vision defects C0025202 Melanoma HSDN C0011991 Loose stools C0856217 Diarrhea functional (due to spastic colon) UMLS C1069915 Vertigo C0032285 Pneumonia HSDN C0009421 Comatose C0160680 Carotid artery injury HSDN C0349506 Sun sensitivity C0432328 Xeroderma pigmentosum, variant form OrphaNet|HPO|MalaCards C0026961 Pupil dilated C0006057 Botulisms OrphaNet|MalaCards C4084773 Bothered by weight gain C0024530 Malaria HSDN C2242996 Tingling C0030305 Pancreatitis HSDN C0019209 Large liver C0016788 Fucosidase deficiency disease OrphaNet|HPO|MalaCards C0019825 Voice hoarseness C0004903 Beckwith-wiedemann syndrome HSDN C0557874 Global developmental delay C0268255 Farber lipogranulomatosis MalaCards|HPO C4085661 Usual severity nausea C0032326 Pneumothorax HSDN C0010038 Corneal opacity disorder C0175778 Larsen syndrome MalaCards C4084774 Have weight loss C1832386 Diabetes mellitus, transient neonatal, 1 OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0018235 Aggrieved HSDN C0151686 Growth retardation C0013364 Dysautonomia, familial OrphaNet|HPO C0019209 Large liver C2748941 Glycogen storage disease, type ixa2 HPO C1579931 Depressed - symptom C0265216 X-linked hydrocephalus syndrome MalaCards C0575081 Abnormal gait C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0042024 Urine incontinence C0003838 Arterial occlusive diseases HSDN C0040485 Wryneck C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards|UMLS C0151827 Pain eye C0038379 Eye deviation HSDN C0013404 Respiratory difficulty C0042214 Vaccinia HSDN C0151825 Ostalgia C0238402 Pycnodysostosis OrphaNet|HPO|MalaCards C0040822 D tremors C2931125 Feigenbaum bergeron richardson syndrome OrphaNet|MalaCards C0027497 Queasy C0026865 Mushroom poisoning HSDN C0012833 Dizzy C0036974 Shock HSDN C0035232 Diaphragmatic paralysis C0342751 Generalized glycogen storage disease of infants MalaCards C0424755 Fever symptoms C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C0007166 Cardiac output decreased C0011881 Diabetic nephropathy HSDN C0037384 Snore C0037315 Sleep apnea syndromes UMLS C4084726 Distress cough C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C2128817 Single skin crust C0153555 Malignant neoplasm of other specified sites of female breast MalaCards C0018772 Deafness C0040997 Trigeminal neuralgia HSDN C2315100 Pediatric failure to thrive C4040739 3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome MalaCards C0018681 Headache, cephalalgia C0025289 Meningitis UMLS C0018991 Paralysis one side of body C0236969 Substance-related disorders HSDN C2984057 Have nausea C1579931 Depressed - symptom HSDN C0032617 High urine output C1999266 Depression adverse event HSDN C0034155 Thrombotic thrombocytopenic purpura C0042974 Von willebrand disease HSDN C4084784 Diarrhea C0206245 Amyloid neuropathies, familial MalaCards C0085606 Urination urgency C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018213 Graves disease HSDN C1963063 Anorexia adverse event C0436596 On examination - apathetic HSDN C4085211 Pain distress question C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C0004134 Dyssynergia C0008626 Congenital chromosomal disease HSDN C2911645 Weight loss adverse event C0033822 Pseudomyxoma peritonei MalaCards C0042510 Fibrillation paroxysmal vent C1859062 Long qt syndrome 3 HPO C0022346 Yellow skin C0023896 Alcoholic liver diseases HSDN|UMLS C0018772 Deafness C0035435 Rheumatism HSDN C4085210 Usual severity pain C0018567 Hand dermatoses HSDN C2911645 Weight loss adverse event C0006105 Brain abscess HSDN C4085548 Usual severity dizziness C0032285 Pneumonia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1456784 Paranoia HSDN C0036572 Convulsion C0863106 Afebrile seizure UMLS C0020578 Hyperventilate C3280479 Pitt-hopkins-like syndrome 2 MalaCards C3463815 Feel fatigue C0950123 Inborn genetic disease HSDN C0004604 Pain back C0543786 Debre's syndrome MalaCards C0015672 Decreased energy C0271270 Oculovestibuloauditory syndrome DiseaseOntology|MalaCards C0241210 Speaking delay C0032897 Prader-willi syndrome MalaCards|HPO C1963093 Dizziness adverse event C0026650 Movement disorders HSDN C3829611 Nausea frequency C0027643 Neoplasm recurrence, local HSDN C1963064 Anxiety adverse event C1837475 Insulin-like growth factor i deficiency MalaCards C0349588 Stature short C0220687 Kbg syndrome MalaCards|HPO C0037384 Snore C0004238 Atrial fibrillation HSDN C1384666 Decreased hearing C1850552 Nephrosis deafness urinary tract digital malformation MalaCards C2919142 Short stature adverse event C0406740 Kohlschutter tonz syndrome MalaCards|HPO C0018772 Deafness C0242952 Behavior infants HSDN C1963067 Atrial fibrillation adverse event C3151267 Cardiomyopathy, familial hypertrophic, 20 HPO C2911645 Weight loss adverse event C2749485 Nblst1 HPO C0027497 Queasy C0038379 Eye deviation HSDN C3641755 Have constipation C0305062 Tetanus toxoids HSDN C4020887 Photodysphoria C0268506 Albinoidism MalaCards C1963252 Tremor adverse event C0349653 Congenital disorder of glycosylation type 1a MalaCards C1557397 Adverse event associated with pain C0004626 Pneumonia, bacterial HSDN C0033774 Skin pruritus C0030286 Pancreatic diseases HSDN C0270948 Neurogenic muscular atrophy C1865294 Pelvic hypoplasia with lower-limb arthrogryposis OrphaNet|MalaCards C3463815 Feel fatigue C0242992 Multiple chemical sensitivity HSDN C0518090 Frequency of pain question C0040156 Thyrotoxicosis HSDN C0020673 Hypothermia (central) (local) C0007194 Hypertrophic cardiomyopathy HSDN C0040460 Dental pain C0152177 Trigeminal neuropathy HSDN C1963137 Hydrocephalus adverse event C0345217 Cloaca exstrophy MalaCards C0030486 Extremity paralysis, lower C0036220 Kaposi sarcoma HSDN C1963091 Diarrhea adverse event C0205788 Histiocytoid hemangioma HSDN C1000483 Genus anemia C0854795 Resectable hepatic malignant neoplasm MalaCards C0518090 Frequency of pain question C0175702 Williams syndrome HSDN C4084774 Have weight loss C1263846 Attention deficit hyperactivity disorder HSDN C0042025 Urinary incontinence stress C0010674 Cystic fibrosis HSDN C0013911 Emaciate C0030500 Animal parasitic disease HSDN C0030200 Intractable pain C1261473 Sarcoma HSDN C0034124 Pupillary disorder C0751815 Carotid artery, internal, dissection HSDN C0018772 Deafness C1847319 Paraganglioma and gastric stromal sarcoma OrphaNet|HPO|MalaCards C0006277 Bronchitis C2750790 Ciliary dyskinesia, primary, 13 MalaCards C0040034 Thrombocytopenia C0035921 Congenital rubella syndrome OrphaNet|MalaCards C0009080 Finger clubbing C1850568 Nakajo syndrome MalaCards|HPO C1963184 Nystagmus adverse event C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0023267 Fibroid tumor HSDN C0020615 Hypoglycemia nos C0751587 Cadasil syndrome HPO C4085548 Usual severity dizziness C0029443 Osteomyelitis HSDN C0036572 Convulsion C0026229 Mite infestation HSDN C2911645 Weight loss adverse event C0206624 Hepatoblastoma MalaCards C4084774 Have weight loss C0518450 Spinal fractures HSDN C4084766 Vomiting C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C4084767 Bothered by vomiting C0017185 Gastrointestinal neoplasms HSDN C4085661 Usual severity nausea C0035204 Respiration disorders HSDN C0149793 Transient monocular blindness C2936350 Plaque, atherosclerotic HSDN C0036572 Convulsion C4015307 Perrault syndrome 5 MalaCards C0031315 Phantom limb pain C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4085210 Usual severity pain C0005283 Beta thalassemia HSDN C0241137 Skin pallor C0024419 Waldenstrom macroglobulinemia OrphaNet|HPO|MalaCards C0009421 Comatose C0023418 Leukemia HSDN C0232513 Premature tooth loss C1859384 Brachioskeletogenital syndrome OrphaNet C0557874 Global developmental delay C1853118 Severe congenital neutropenia HPO C0019572 Hairiness C1838257 Serpentine fibula polycystic kidney syndrome MalaCards C1557397 Adverse event associated with pain C0751878 Vasculitis, central nervous system HSDN C0026838 Spasticity muscle C0268496 Kramer syndrome OrphaNet|MalaCards C4084774 Have weight loss C3146222 Idiopathic aortitis MalaCards C0013911 Emaciate C0206247 Amyloid neuropathies HSDN C0917816 Deficiency mental C0265354 Charge syndrome OrphaNet|HPO|MalaCards C1279888 Proteinuria of undiagnosed cause C0597109 Nurse's role HSDN C0522224 Palsied C0997768 Glaucoma HSDN C0427055 Face weakness C1334698 Meningothelial cell neoplasm MalaCards C0002622 Amnesias C0029941 Brief psychiatric rating scale HSDN C0018681 Headache, cephalalgia C0346304 Gonadotroph adenoma MalaCards C0018681 Headache, cephalalgia C0004364 Autoimmune diseases HSDN C4084784 Diarrhea C0042138 Uterine neoplasms HSDN C0035229 Respiratory function impaired C2931282 Skeletal dysplasia, san diego type OrphaNet|HPO|MalaCards C0033774 Skin pruritus C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4084774 Have weight loss C2749484 Neuroblastoma, susceptibility to HPO C2911647 Weight gain adverse event C0019693 Hiv infections HSDN C0036572 Convulsion C2752008 Spastic paraplegia-50, autosomal recessive MalaCards|HPO|UMLS C1557397 Adverse event associated with pain C0028758 Bonding HSDN C0042571 Vertigo subjective C0023267 Fibroid tumor HSDN C4085210 Usual severity pain C0033845 Pseudotumor cerebri HSDN C0009676 Confusion state C0014859 Esophageal neoplasms HSDN C0031911 Pigment deposition C2931912 Mende syndrome MalaCards C0012569 Double vision C0003855 Arteriovenous fistula HSDN C1963087 Constipation adverse event C0878683 Pituitary dwarfism type 3 MalaCards C0018772 Deafness C0011615 Dermatitis, atopic HSDN C1860844 Sparse, thin hair C1835492 Tooth agenesis, selective, 4 (disorder) MalaCards C1850830 Exercise-induced muscle pain C0268149 Glycogen storage disease type x MalaCards|HPO C3641756 Have diarrhea C0398623 Thrombophilia HSDN C4084802 Usual severity diarrhea C0344423 Atrial flutter by ecg finding HSDN C3274924 Have been coughing C0018824 Heart valve disease HSDN C0424755 Fever symptoms C0085207 Gestational diabetes HSDN C3887638 Failure to thrive in infant C0549567 Pigmentation disorders HSDN C1963087 Constipation adverse event C1869118 Hypothyroidism, congenital, due to thyroid dysgenesis HPO C1963137 Hydrocephalus adverse event C1849409 Knobloch syndrome OrphaNet|HPO|MalaCards C3541349 Syncope C0262584 Carcinoma, small cell HSDN C0004134 Dyssynergia C0013808 Electroconvulsive therapy HSDN C0242670 Chronic vegetative state C1962963 Osteoporosis adverse event HSDN C1962972 Proteinuria adverse event C0585442 Osteosarcoma of bone HSDN C2919142 Short stature adverse event C0398788 Immunodeficiency syndrome, variable MalaCards|HPO C0152459 Striae C0342442 Acth-dependent cushing's syndrome OrphaNet C0020458 Hyperhydrosis C0023931 Lobstein's disease OrphaNet C0030554 Abnormal sensation C0012644 Animal disease models HSDN C3815497 Cough C0036467 Scrofula MalaCards C0027497 Queasy C0025063 Mediastinal neoplasms HSDN C0002962 Angina C3814778 Hemolytic index HSDN C3641756 Have diarrhea C0239981 Hypoalbuminemia HSDN C0344315 Mood depressed C2930815 Acute cerebral gaucher disease MalaCards C1384666 Decreased hearing C3494419 Deformities, dentofacial HSDN C0522224 Palsied C0029185 Orbit tumor HSDN C0012569 Double vision C0027765 Nervous system disorder HSDN C0002622 Amnesias C0011194 Deja-vu HSDN C0242936 Center pain C0023290 Leishmaniasis, visceral HSDN C1963063 Anorexia adverse event C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0013390 Cramps menstrual C0036341 Schizophrenia HSDN C3887873 Hearing loss C0013336 Dwarfism HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033806 Pseudohypoparathyroidism HSDN C0000737 Abdomen pain C0346170 Benign ovarian serous cystadenoma UMLS C4084775 Usual severity weight loss C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0020455 Hypergammaglobulinemia C0023281 Leishmaniasis OrphaNet|HSDN|MalaCards C1090821 Sepsis C0004368 Autoimmune state MalaCards C0018681 Headache, cephalalgia C0475523 Spinal+epidural anesthesia-inducd headache during pregnancy UMLS C0018926 Emesis bloody C0002726 Amyloidosis HSDN C3815497 Cough C0549472 Pneumonia, cholesterol MalaCards C1963071 Back pain adverse event C0002453 Amenorrhea HSDN C4085548 Usual severity dizziness C0016658 Fracture bone HSDN C0162298 Stiffness joints C1836602 Bruck syndrome 2 OrphaNet|HPO|MalaCards C0013362 Dysarthrias C1876175 Ataxia-telangiectasia variant MalaCards|HPO C4042891 Sleep wake disorders C0271650 Impaired glucose tolerance HSDN C0851578 Disorder sleep C0006107 Concussion HSDN C2024878 Cardiovascular surgery result: dyspnea C0041321 Tuberculosis, miliary HSDN C1963093 Dizziness adverse event C0037313 Sleep HSDN C3887873 Hearing loss C0007117 Basal cell carcinoma HSDN C0277959 Hair coarseness C2931168 Hemangiomas, and cutaneous and intracranial vascular deformations MalaCards C0039870 Leanness C0036239 Satiety HSDN C4084774 Have weight loss C0085271 Self-injurious behavior HSDN C1950154 Insomnia homeopathic medication C0751254 Creutzfeldt-jakob disease, familial MalaCards C0040264 Ear ringing sound C1962963 Osteoporosis adverse event HSDN C0042025 Urinary incontinence stress C0003467 Anxiety HSDN C4084784 Diarrhea C0242350 Erectile dysfunction HSDN C4084773 Bothered by weight gain C0597109 Nurse's role HSDN C0020673 Hypothermia (central) (local) C0014761 Erythroblastosis, fetal HSDN C0022568 Inflammation corneal C1865181 Mandibulofacial dysostosis with macroblepharon and macrostomia MalaCards C0019572 Hairiness C2936862 Bardet-biedl syndrome 1 (disorder) MalaCards C0037199 Sinus infection C1847554 Ciliary dyskinesia, primary, 2 (disorder) MalaCards|HPO C1963137 Hydrocephalus adverse event C1856051 Daish hardman lamont syndrome MalaCards C3887873 Hearing loss C0008924 Cleft lip HSDN C0151786 Weakness muscle C1412084 Abcd1 gene HSDN C0003862 Pain joint C0041466 Typhoid fever OrphaNet|MalaCards C0040822 D tremors C0014060 Encephalitis, st. louis DiseaseOntology|HSDN|MalaCards C0018784 Deafness sensorineural C1970827 Phosphoribosylpyrophosphate synthetase superactivity MalaCards|HPO C0013604 Edematous C0005604 Trauma birth HSDN C4084775 Usual severity weight loss C0687150 Parathyroid gland adenocarcinoma OrphaNet|HPO|MalaCards C0018808 Murmur C4049644 Depression HSDN C0522224 Palsied C0006057 Botulisms MalaCards C4085211 Pain distress question C0036920 Sezary syndrome HSDN C3829611 Nausea frequency C1847839 Episodic ataxia, type 3 MalaCards C1549543 Administration method - pain C0025500 Mesothelioma HSDN C0018524 Hallucinate C2675891 Chromosome 1q21.1 duplication syndrome MalaCards C1963086 Confusion adverse event C0032087 Plant poisoning HSDN C1384666 Decreased hearing C0029342 Orthomyxoviridae infections HSDN C3146279 Coma C0025637 Methemoglobinemia HSDN C0030232 Color loss C0034212 Pyoderma HSDN C4085862 Bothered by nausea C0020517 Hypersensitivity HSDN C0030554 Abnormal sensation C0238154 Epidural hematoma HSDN C0031911 Pigment deposition C0043346 Xeroderma pigmentosum MalaCards C1963091 Diarrhea adverse event C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0917801 Sleep disorder insomnia C3888867 Agrypnia UMLS C1971624 Appetite absent C0238386 Cronkhite-canada disease MalaCards C2024893 Cardiovascular surgery result: fatigue C0018805 Heart injuries HSDN C3641756 Have diarrhea C0409959 Osteoarthritis, knee HSDN C0000737 Abdomen pain C2987170 Pancreatic macrocystic serous cystadenoma UMLS C1279888 Proteinuria of undiagnosed cause C0041956 Ureteral obstruction HSDN C4085210 Usual severity pain C0015556 Fallopian tube diseases HSDN C0575081 Abnormal gait C3888090 Early onset torsion dystonia OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0339959 Pneumonia chlamydial HSDN C2129518 Lower back pain radiating to right groin C1857718 Cataract, posterior polar, 5 MalaCards C0040822 D tremors C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO|UMLS C0520909 Ponv C1963254 Tumor lysis syndrome adverse event HSDN C4084784 Diarrhea C0038220 Status epilepticus HSDN C0014591 Bleeding nose C2931916 Midline granulomatosis MalaCards C4084802 Usual severity diarrhea C1009209 Tinea HSDN C4084726 Distress cough C0003467 Anxiety HSDN C4050613 Anxiety C0393639 Hashimoto's encephalitis MalaCards C0000737 Abdomen pain C1969419 Pancreatitis, chronic, susceptibility to HPO C0013604 Edematous C0008479 Chondrosarcoma HSDN C2896434 Metatarsalgia, left foot C3864027 Bilateral metatarsalgia UMLS C0018989 Paresis of one side of body C1832903 Migraine, sporadic hemiplegic HPO C3665492 Pigmentations C1305256 Angiolipoma, infiltrating MalaCards C1963091 Diarrhea adverse event C0043241 Wound infection HSDN C0018524 Hallucinate C0600104 Obsessive compulsive behavior HSDN C4084768 Usual severity vomiting C0024530 Malaria HSDN C1963091 Diarrhea adverse event C2911243 Encounter due to family history of colonic polyps HSDN C0086437 Joint hypermobility C2674574 Aortic aneurysm, familial thoracic 3 MalaCards|UMLS C0038506 Stutter C1579931 Depressed - symptom HSDN C2024878 Cardiovascular surgery result: dyspnea C0029443 Osteomyelitis HSDN C0036572 Convulsion C4015080 Microcephaly 13, primary, autosomal recessive MalaCards C0030554 Abnormal sensation C0042138 Uterine neoplasms HSDN C4042891 Sleep wake disorders C1168250 Laryngopharyngeal reflux HSDN C0042940 Disorder of voice C0012644 Animal disease models HSDN C3898969 Have been vomiting C1335398 Gastric peutz-jeghers polyp MalaCards C0032617 High urine output C0266463 Lissencephaly HSDN C0042025 Urinary incontinence stress C0037369 Smoking HSDN C0013362 Dysarthrias C0006107 Concussion HSDN C0018784 Deafness sensorineural C0149514 Bronchitis acute HSDN C4084724 Usual severity constipation C0997768 Glaucoma HSDN C0009676 Confusion state C0018946 Hematoma, subdural HSDN C0013404 Respiratory difficulty C0007784 Cerebral hemisphere hemorrhage HSDN C0848203 Male pelvic pain C1548578 Location characteristic id - smoking HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1963274 Vasculitis adverse event HSDN C0020672 Body temperature decreased C0032851 Disease poultry HSDN C0020305 Fetal edema C0024121 Lung neoplasms HSDN C4084724 Usual severity constipation C0017075 Ganglioneuroma HSDN C3815497 Cough C0037051 Behavior illness HSDN C1549543 Administration method - pain C0006107 Concussion HSDN C0000737 Abdomen pain C0013386 Dyskinesia, drug-induced HSDN C1963249 Tinnitus adverse event C3810814 Myocardial infarction ecg assessment HSDN C4085317 Diarrhea frequency C0342859 Harderoporphyria HPO C0242936 Center pain C0014356 Enterocolitis HSDN C2919142 Short stature adverse event C1834969 Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly HPO C1384666 Decreased hearing C2931643 Madokoro ohdo sonoda syndrome MalaCards C0234146 Absent reflex C0393808 Charcot-marie-tooth disease, x-linked, 1 OrphaNet|HPO C0015469 Facial paralysis C0265234 Branchio-oto-renal syndrome MalaCards|HPO C1963087 Constipation adverse event C0039145 Syringomyelia and syringobulbia HSDN C0039231 Heartbeats increased C1868633 Paragangliomas with sensorineural hearing loss HPO C1963252 Tremor adverse event C0010346 Crohn disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2616767 Mycetoma HSDN C4084724 Usual severity constipation C1856113 Mowat-wilson syndrome MalaCards|HPO C2911645 Weight loss adverse event C3489413 Lipomatosis, multiple HSDN C4085661 Usual severity nausea C0003467 Anxiety HSDN C0015468 Face pain C0029456 Osteoporosis HSDN C4084773 Bothered by weight gain C0043168 Whooping cough due to unspecified organism HSDN C1963093 Dizziness adverse event C0006309 Brucellosis HSDN C1549543 Administration method - pain C0024689 Mandibular diseases HSDN C0151767 Liver tenderness of C0267792 Hepatobiliary disease UMLS C0234523 Apraxia, classic C0015347 Extinction HSDN C2911645 Weight loss adverse event C0021359 Infertility HSDN C4084776 Weight loss C0029928 Ovarian diseases HSDN C0518090 Frequency of pain question C0013533 Echovirus infections HSDN C3714552 Strength decreased C0035410 Rhabdomyolysis UMLS C0751837 Gait ataxic C1527336 Sjogren's syndrome HSDN C0750937 Appendicular ataxia C1836395 Spinocerebellar ataxia 26 HPO C0007859 Pain neck C0036341 Schizophrenia HSDN C0018681 Headache, cephalalgia C0027927 Neurosyphilis HSDN C0000737 Abdomen pain C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C0151908 Dry skin C0751435 Hyperphenylalaninaemia MalaCards C1549543 Administration method - pain C0677838 Grief loss HSDN C0036572 Convulsion C0023269 Leiomyosarcoma HSDN C0413252 Hypothermia due to exposure C0033975 Psychotic disorders HSDN C0030193 Sense of pain C1332303 Adenoid cystic carcinoma of anterior tongue UMLS C0518090 Frequency of pain question C0015302 External exotoses HSDN C3898969 Have been vomiting C0021833 Intestinal fistula HSDN C0026826 High muscle tone C2931226 Thompson baraitser syndrome OrphaNet|MalaCards C0278152 Hemifacial spasms C0338480 Common migraine HSDN C0026821 Cramp C0018193 Granuloma, foreign-body HSDN C2032396 Pelvic pain on the right C0205788 Histiocytoid hemangioma HSDN C0018681 Headache, cephalalgia C0018133 Graft-vs-host disease HSDN C0162298 Stiffness joints C0032533 Polymyalgia rheumatica MalaCards C1963252 Tremor adverse event C0024473 Magnesium deficiency HSDN C0033377 Caudal displacement C1844934 Arthrogryposis multiplex congenita, distal, x-linked HPO C2315100 Pediatric failure to thrive C1835849 Congenital disorder of glycosylation, type im MalaCards|HPO C4084723 Constipation C0850803 Anaphylaxis (non medication) HSDN C0009421 Comatose C0024776 Maple syrup urine disease HSDN|HPO C1963087 Constipation adverse event C0034885 Rectal neoplasms HSDN C3887638 Failure to thrive in infant C1963107 Euphoria adverse event HSDN C0241165 Skin thickening C1850155 Torg-winchester syndrome MalaCards|HPO C1384666 Decreased hearing C0265289 Metaphyseal chondrodysplasia schmid type OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0033788 Pseudo-hurler polydystrophy MalaCards C3898969 Have been vomiting C0752165 Angioma, venous, central nervous system HSDN C0036572 Convulsion C1863924 Megalanecephaly polymicrogyria-polydactyly hydrocephalus syndrome OrphaNet|HPO|MalaCards C1963086 Confusion adverse event C0151620 Hypertensive encephalopathy HSDN C0030794 Pelvis pain C0020550 Hyperthyroidism HSDN C1069915 Vertigo C0024115 Lung diseases HSDN C0522224 Palsied C0004626 Pneumonia, bacterial HSDN C0003962 Ascites C1856306 Gsd iv, neuromuscular form, adult, with isolated myopathy HPO C3146279 Coma C0031212 Personality disorders HSDN C0042514 Ventricular tachycardia C1837839 Cardiomyopathy, dilated, 1o MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C1302282 Chromaffin cell neoplasm MalaCards C0497406 Over weight C0011168 Deglutition disorders HSDN C0037384 Snore C0013117 Dreaming HSDN C3815497 Cough C0024899 Mastocytosis MalaCards C0037763 Spasm C0042029 Urinary tract infection HSDN C0038002 Spleen enlargement C2700553 Omenn syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0013182 Drug allergy HSDN C0005779 Clotting C0019156 Hepatic veno-occlusive disease OrphaNet C0030794 Pelvis pain C0242350 Erectile dysfunction HSDN C0917801 Sleep disorder insomnia C0162531 Hereditary coproporphyria HPO C0019825 Voice hoarseness C0009946 Conversion disorder HSDN C4085317 Diarrhea frequency C0241932 X-linked hypogammaglobulinemia HPO C0018681 Headache, cephalalgia C0007138 Carcinoma, transitional cell HSDN C0085636 Light sensitivity C0349606 Central nervous system cysts HSDN C0162429 Dietary deficiency C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C3489393 Hiatal hernia HSDN C0151686 Growth retardation C3809875 Van maldergem syndrome 2 MalaCards C0029163 Hemorrhage mouth C0040434 Discoloration tooth HSDN C1963170 Hypothermia adverse event C0003615 Appendicitis HSDN C0427055 Face weakness C1840404 Hyperostosis cranialis interna MalaCards C0917816 Deficiency mental C0948368 Kaufman-mckusick syndrome MalaCards|HPO C2203646 Jaundice C0032229 Pleural neoplasms HSDN C0085602 Polydypsia C0020437 Hypercalcemia HSDN C1961131 Cough adverse event C0018200 Granuloma, respiratory tract HSDN C0423365 Vitreous inflammatory infiltrate C1563272 Vitreous snowballs UMLS C0270948 Neurogenic muscular atrophy C3888102 Frontotemporal dementia with motor neuron disease MalaCards C0033377 Caudal displacement C0475813 Alpha thalassemia-mental retardation syndrome MalaCards C0520966 Coordination impaired C3888031 Spinocerebellar ataxia 35 MalaCards|UMLS C0159063 Other urination abnormality C0810038 Genitourinary symptoms and ill-defined conditions UMLS C0020672 Body temperature decreased C0009373 Colonic diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0032708 Disorders of porphyrin metabolism OrphaNet|HSDN|MalaCards C1557397 Adverse event associated with pain C0003949 Asbestosis HSDN C4084769 Vomiting frequency C0018273 Growth disorders HSDN C3203358 Alveolar hypoventilation C0021295 Infant, premature, diseases HSDN C0011991 Loose stools C0033054 Prenatal exposure delayed effects HSDN C4084767 Bothered by vomiting C0497327 Dementia HSDN C4085549 Dizziness C0023890 Liver cirrhosis HSDN C3463815 Feel fatigue C1548777 Specimen reject reason - hemolysis HSDN C1963091 Diarrhea adverse event C0037650 Somatoform disorder HSDN C0018784 Deafness sensorineural C1832200 Peroxisome biogenesis disorders HPO C0036572 Convulsion C0162532 Variegate porphyria MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0041948 Uremia HSDN C1963247 Ventricular tachycardia adverse event C2678476 Cardiomyopathy, dilated, 1y MalaCards|HPO C1963252 Tremor adverse event C0268151 Classical galactosemia MalaCards|HPO C1557397 Adverse event associated with pain C0000833 Abscess HSDN C1962972 Proteinuria adverse event C0342337 Insulin resistance syndrome, type b OrphaNet|MalaCards C0542476 Forgetful C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C0000727 Abdomen acute C0034183 Pyelitis unspecified HSDN C0040822 D tremors C1850100 Parkinson disease 15, autosomal recessive (disorder) HPO|UMLS C3641756 Have diarrhea C1834211 Ganglioneuromatosis of the alimentary tract HPO C2024878 Cardiovascular surgery result: dyspnea C0002949 Aneurysm, dissecting HSDN C0557874 Global developmental delay C3280215 Holoprosencephaly 11 MalaCards C0007859 Pain neck C1962986 Glaucoma adverse event HSDN C2911647 Weight gain adverse event C0037322 Active eye movement sleep HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0017536 Giardiasis DiseaseOntology|HSDN C1557397 Adverse event associated with pain C1704275 Pyomyositis HSDN C0233794 Memory impaired C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0030232 Color loss C0031511 Pheochromocytoma MalaCards|HSDN C0036572 Convulsion C1999266 Depression adverse event HSDN C2984058 Have pain C0027707 Nephritis, interstitial HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2984330 Chagas disease pathway HSDN C3815497 Cough C0524799 Hyperlucent lung HSDN C0011206 Delirium acute C0011854 Diabetes mellitus, insulin-dependent HSDN C1557397 Adverse event associated with pain C0161410 Accessory nerve injuries HSDN C0424755 Fever symptoms C1705812 Nci thesaurus role HSDN C2032396 Pelvic pain on the right C0006663 Calcinosis HSDN C4084727 Cough frequency C0031090 Periodontal diseases HSDN C1963091 Diarrhea adverse event C0022729 Klebsiella infections HSDN C1557397 Adverse event associated with pain C0022595 Keratosis follicularis HSDN C3146279 Coma C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C0013362 Dysarthrias C3150169 Frontotemporal lobar degeneration with tdp43 inclusions, tardbp-related HPO C1145670 Failure respiratory C0034960 Refsum disease HPO C0020455 Hypergammaglobulinemia C0263662 Disseminated eosinophilic collagen disease HSDN C0851578 Disorder sleep C2137063 Ent surgical result - speech HSDN C0020450 Hyperemesis gravidarum C0405080 Hyperem.gravid.+metab.dist.nos UMLS C0242936 Center pain C0014547 Epilepsies, partial HSDN C2203646 Jaundice C0034067 Pulmonary emphysema HSDN C4084768 Usual severity vomiting C0078981 Arachnoid cysts HSDN C4084766 Vomiting C1522136 Hypernatremia result HSDN C0019209 Large liver C3151000 Hemorrhagic destruction of the brain, subependymal calcification, and cataracts MalaCards|HPO C0036572 Convulsion C0001723 Affective disorders, psychotic HSDN C0851578 Disorder sleep C0020459 Hyperinsulinism HSDN C0011206 Delirium acute C0040479 Torsades de pointes HSDN C4085548 Usual severity dizziness C0034067 Pulmonary emphysema HSDN C0015672 Decreased energy C3658239 D personality, type HSDN C0039070 Collapse fleeting C0039685 Tetralogy of fallot HSDN C0015938 Fetal macrosomia C0269886 Inversion of uterus HSDN C0009421 Comatose C0014852 Esophageal diseases HSDN C1963274 Vasculitis adverse event C0343101 Wells syndrome MalaCards C2911645 Weight loss adverse event C2911643 Encounter due to family history of osteoporosis HSDN C1963164 Lymphopenia adverse event C1858664 Hemochromatosis, type 3 MalaCards C0234428 Consciousness disturbance C0751666 Canavan disease, infantile MalaCards C2984057 Have nausea C1856401 Etfa deficiencies HPO C4085211 Pain distress question C0011630 Dermatomycoses HSDN C1549543 Administration method - pain C0520720 Cyst nerve root HSDN C0020455 Hypergammaglobulinemia C0027721 Lipoid nephrosis HSDN C0426579 Anorexia symptom C1527406 Rhizomelic pseudopolyarthritis MalaCards C4084725 Usual severity cough C2984289 Melanoma pathway HSDN C0522224 Palsied C0018235 Aggrieved HSDN C0349588 Stature short C0010495 Cutis laxa OrphaNet|MalaCards C0221263 Cafe au lait spot C2931622 Ring chromosome 7 MalaCards C0917816 Deficiency mental C3281235 Baraitser-winter syndrome 2 MalaCards C0030232 Color loss C3150986 Epileptic encephalopathy, early infantile, 7 MalaCards C0028738 Nystagmus C2700405 Waardenburg syndrome, type iie HPO C1963087 Constipation adverse event C0151516 Thyroid hypoplasia OrphaNet|HPO C3539022 Pelvic pain decreasing in severity C0021359 Infertility HSDN C1963170 Hypothermia adverse event C3489413 Lipomatosis, multiple HSDN C3641756 Have diarrhea C0206172 Diabetic foot HSDN C0030193 Sense of pain C1299438 Angina recurrent status post coronary artery bypass graft UMLS C0023380 Lethargy C0014356 Enterocolitis HSDN C4050613 Anxiety C0268631 Succinic semialdehyde dehydrogenase deficiency MalaCards|HPO C0026838 Spasticity muscle C0432328 Xeroderma pigmentosum, variant form MalaCards C1384666 Decreased hearing C1578691 Congenital myxedema MalaCards C0022660 Acute kidney failure C0221021 Microangiopathic hemolytic anemia MalaCards C0024032 Birth weight subnormal C0432267 Tricho thiodystrophy disorder MalaCards|HPO C4085211 Pain distress question C0006110 Brain death HSDN C0033377 Caudal displacement C1837819 Cerebrofrontofacial syndrome MalaCards C3541349 Syncope C1263846 Attention deficit hyperactivity disorder HSDN C1962972 Proteinuria adverse event C1306856 Megaloblastic anemia due to inborn errors of metabolism HPO C4084727 Cough frequency C0022408 Arthropathy HSDN C0577564 Mass of lymphoreticular structure C0346979 Secondary malignant neoplasm of bone marrow UMLS C2911647 Weight gain adverse event C0031511 Pheochromocytoma HSDN C0012833 Dizzy C0477455 Other disorders of vestibular function, unspecified ear UMLS C0017181 Gastrointestinal bleed C0263666 Dermatomyositis, childhood type MalaCards C0042571 Vertigo subjective C0024841 Matrimony, matrimonial HSDN C0000731 Abdomen distention C0266209 Congenital dilatation of colon MalaCards C3539891 Pelvic pain to the rear C0242669 Placenta retained HSDN C0242936 Center pain C0035613 Rift valley fever HSDN C0520909 Ponv C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0242936 Center pain C0024137 Lupus erythematosus, cutaneous HSDN C3463815 Feel fatigue C0020635 Hypopituitarism HSDN C0020455 Hypergammaglobulinemia C3714644 Thymus neoplasms HSDN C4049644 Depression C2932716 Pseudohypoparathyroidism type 1c HPO C0009421 Comatose C0022658 Kidney diseases HSDN C0020305 Fetal edema C0152095 Patau syndrome OrphaNet|MalaCards C0034150 Skin purpura C0034088 Pulmonary valve insufficiency HSDN C0018524 Hallucinate C0010068 Coronary heart disease HSDN C0018784 Deafness sensorineural C1840333 Barakat syndrome HPO C3714552 Strength decreased C3276432 Multiple mitochondrial dysfunctions syndrome 1 MalaCards|UMLS C0151908 Dry skin C1510460 Orofaciodigital syndrome i MalaCards|HPO C4042891 Sleep wake disorders C0238288 Muscular dystrophy, facioscapulohumeral HSDN C0042384 Vasculitis, nonspecific C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0042571 Vertigo subjective C0034069 Pulmonary fibrosis HSDN C1510456 Wernicke aphasia C0032787 Postoperative complications HSDN C0030552 Paralysis partial C0019693 Hiv infections HSDN C0010200 Cough symptom C0034072 Cor pulmonale HSDN C0030193 Sense of pain C0206644 Histiocytoma, benign fibrous HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0038358 Gastric ulcer HSDN C0003862 Pain joint C0206653 Angiomyoma HSDN C0242936 Center pain C0014457 Eosinophilia HSDN C0033774 Skin pruritus C0011311 Dengue fever OrphaNet|HSDN|MalaCards C3641755 Have constipation C0342859 Harderoporphyria HPO C0085636 Light sensitivity C0006035 Borrelia infections MalaCards C0033774 Skin pruritus C0022650 Kidney calculi HSDN C1963091 Diarrhea adverse event C0206247 Amyloid neuropathies MalaCards C0233514 Behavior abnormal C2936346 22q11 deletion syndrome MalaCards C0004941 Behavioral symptoms C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C0018808 Murmur C0009450 Disease caused by microorganism HSDN C1963063 Anorexia adverse event C0004096 Asthma HSDN C0424755 Fever symptoms C4080064 Autosomal dominant hereditary pancreatitis MalaCards C0042571 Vertigo subjective C2984330 Chagas disease pathway HSDN C4084726 Distress cough C0007137 Squamous cell carcinoma HSDN C0030193 Sense of pain C0039082 Syndrome HSDN C1961131 Cough adverse event C1552527 Clinic / center - developmental disabilities HSDN C4084776 Weight loss C0014170 Endometrial neoplasms HSDN C4084784 Diarrhea C0238154 Epidural hematoma HSDN C3539890 Pelvic pain causes awakening at night C0243001 Abdominal abscess HSDN C0557874 Global developmental delay C1863728 Hemophagocytic lymphohistiocytosis, familial, 4 MalaCards|HPO C0019572 Hairiness C0041296 Tuberculosis HSDN C4049644 Depression C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C0030486 Extremity paralysis, lower C0033873 Psychiatry HSDN C0018681 Headache, cephalalgia C1334227 Internal auditory canal meningioma UMLS C0030193 Sense of pain C0041955 Ureteral neoplasms HSDN C3641756 Have diarrhea C0040954 Infection by trichuris trichiura DiseaseOntology|MalaCards C1549543 Administration method - pain C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C1549543 Administration method - pain C0009062 Clostridia infection HSDN C2919142 Short stature adverse event C2748571 Isolated growth hormone deficiency, type ib HPO C0151786 Weakness muscle C0023895 Liver diseases HSDN C0004093 Asthenia C0001621 Adrenal gland diseases HSDN C0013604 Edematous C0027149 Myxoma HSDN C0033774 Skin pruritus C0206654 Leiomyomatosis HSDN C2024878 Cardiovascular surgery result: dyspnea C0010054 Coronary arteriosclerosis HSDN C1963087 Constipation adverse event C1550672 Specimen type - ulcer HSDN C1557397 Adverse event associated with pain C0022568 Keratitis HSDN C1549543 Administration method - pain C0034091 Pulmonary veno-occlusive disease (disorder) HSDN C2911647 Weight gain adverse event C0021799 Interprofessional relations HSDN C3641756 Have diarrhea C0032851 Disease poultry HSDN C0026821 Cramp C0032965 Pregnancy complications, infectious HSDN C0917816 Deficiency mental C0344467 Biemond syndrome MalaCards C0019214 Hepatosplenomegaly C1835916 Aicardi-goutieres syndrome 3 MalaCards|HPO C0086565 Liver function abnormal C2750069 Lipodystrophy, congenital generalized, type 4 OrphaNet|HPO|MalaCards C0013604 Edematous C1623041 Breast-fed HSDN C0007166 Cardiac output decreased C0042510 Ventricular fibrillation HSDN C2237041 Shox gene with short stature C0265316 Neurocutaneous syndromes MalaCards C1963063 Anorexia adverse event C0002986 Fabry disease OrphaNet|HPO|MalaCards C0020673 Hypothermia (central) (local) C0085426 Gram-positive bacterial infections HSDN C0037316 Not enough sleeping C0021831 Intestinal diseases HSDN C0002965 Crescendo angina C0011615 Dermatitis, atopic HSDN C2362324 Pediatric obesity C0033806 Pseudohypoparathyroidism HSDN C2024893 Cardiovascular surgery result: fatigue C0007097 Carcinomas HSDN C1384666 Decreased hearing C1863090 Alopecia, epilepsy, pyorrhea, mental subnormality MalaCards C1963093 Dizziness adverse event C0020619 Hypogonadism HSDN C3898969 Have been vomiting C0009324 Ulcerative colitis HSDN C4084726 Distress cough C0796561 Melanoma vaccines HSDN C4084775 Usual severity weight loss C0020473 Hyperlipidemia HSDN C0024032 Birth weight subnormal C1851402 Exudative vitreoretinopathy 1 MalaCards C3887873 Hearing loss C0026705 Mucopolysaccharidosis ii HSDN C0017672 Pain tongue C0039494 Temporomandibular joint disorders HSDN C0030193 Sense of pain C0035086 Renal osteodystrophy HSDN C3641756 Have diarrhea C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0850758 Pain pelvic C0085096 Peripheral vascular diseases HSDN C1963170 Hypothermia adverse event C0030922 Peptic ulcer hemorrhage HSDN C0018784 Deafness sensorineural C0039128 Syphilis HSDN C2237041 Shox gene with short stature C3891452 Seckel syndrome 8 MalaCards C4085549 Dizziness C0003864 Arthritis HSDN C2984058 Have pain C0037889 Hereditary spherocytosis HSDN C4084725 Usual severity cough C0003962 Ascites HSDN C4084773 Bothered by weight gain C0003864 Arthritis HSDN C0043094 Weight gain C0018671 Head and neck neoplasms HSDN C0024032 Birth weight subnormal C2678415 Hyperphenylalaninemia, bh4-deficient, due to partial pts deficiency HPO C0460137 Push down or depress C1563715 Andersen syndrome HPO C2875626 Eyelid retraction right eye, unspecified eyelid C0015397 Disorder of eye UMLS C0476273 Distress respiratory C1842691 Diaphanospondylodysostosis OrphaNet|HPO|MalaCards C3541349 Syncope C3815186 Ager wt allele HSDN C1279888 Proteinuria of undiagnosed cause C0036946 Sheep--diseases HSDN C0030552 Paralysis partial C0751871 Autoimmune diseases of the nervous system HSDN C0013604 Edematous C0018939 Hematological disease HSDN C3898969 Have been vomiting C1963274 Vasculitis adverse event HSDN C4084723 Constipation C0338503 Septo-optic dysplasia HPO C0010520 Skin cyanosis C0017178 Gastrointestinal diseases HSDN C0013609 Oedema, localised C0235438 Sacral edema UMLS C4084768 Usual severity vomiting C0020732 Iatrogenic disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0021141 Inappropriate adh syndrome HSDN C4049602 Hyperactivity C2713347 7-dehydrocholesterol reductase deficiency MalaCards C0151908 Dry skin C2314896 Familial atypical mole melanoma syndrome OrphaNet|HPO C0000737 Abdomen pain C1848586 Intestinal pseudoobstruction with external ophthalmoplegia MalaCards C0004310 Auditory disorder process C0236969 Substance-related disorders HSDN C4084774 Have weight loss C0038644 Sudden infant death syndrome HSDN C0015970 Fever unknown origin C1963198 Pancreatitis adverse event HSDN C0020578 Hyperventilate C0036986 Shock, traumatic HSDN C0018772 Deafness C0027927 Neurosyphilis HSDN C0812426 Kidney problem C0266292 Congenital anomaly of the kidney UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0036349 Paranoid schizophrenia HSDN C2029884 Hearing loss by exam C0019562 Von hippel-lindau syndrome HSDN C2024893 Cardiovascular surgery result: fatigue C0007131 Non-small cell lung carcinoma HSDN C1963091 Diarrhea adverse event C0020452 Hyperemia HSDN C0042798 Vision dim C0268506 Albinoidism MalaCards C3645888 Urinary incontinence gradual onset C0042024 Urinary incontinence UMLS C0232466 Feeding difficulty C4015447 Combined oxidative phosphorylation deficiency 23 MalaCards C4084769 Vomiting frequency C0037933 Spinal diseases HSDN C0015230 Exanthem C1847319 Paraganglioma and gastric stromal sarcoma MalaCards C4084774 Have weight loss C0040100 Thymoma HSDN C0033774 Skin pruritus C0007131 Non-small cell lung carcinoma HSDN C4084768 Usual severity vomiting C0006147 Breast fed HSDN C0042963 Symptoms vomiting C0405075 Other preg.vomiting unspecif. UMLS C0002622 Amnesias C0002726 Amyloidosis HSDN C3539020 Pelvic pain decreasing in frequency C0026769 Multiple sclerosis HSDN C0004134 Dyssynergia C0023264 Leigh disease OrphaNet|UMLS|HPO|MalaCards C0155502 Vertigo benign positional C0393735 Headache disorders HSDN C1557397 Adverse event associated with pain C0036899 Abstinence sex HSDN C0042963 Symptoms vomiting C0008149 Chlamydia infections HSDN C0030232 Color loss C0023290 Leishmaniasis, visceral HSDN C4085211 Pain distress question C0007117 Basal cell carcinoma HSDN C0003811 Cardiac rhythm disturbance C1858592 Carney triad MalaCards C0557874 Global developmental delay C1853153 Joubert syndrome 6 MalaCards|HPO C0030552 Paralysis partial C0272126 Evans syndrome OrphaNet|MalaCards C0398650 Idiopathic thrombocytopenia purpura C1552262 Nurse practitioner - family HSDN C0151786 Weakness muscle C0017924 Glycogen storage disease type v HPO C0973461 Dysphasia C2717836 Steroid sulfatase deficiency disease MalaCards C1963071 Back pain adverse event C0597109 Nurse's role HSDN C0013395 Indigestion C0027707 Nephritis, interstitial HSDN C4084773 Bothered by weight gain C0004044 Asphyxia HSDN C4085210 Usual severity pain C0002886 Anemia, macrocytic HSDN C3887638 Failure to thrive in infant C0268448 Primary hypomagnesemia (disorder) MalaCards|HPO C1963063 Anorexia adverse event C0023601 Leydig cell tumor HSDN C0007859 Pain neck C0036677 Sensory threshold HSDN C0023012 Delay language C3281138 Chromosome 17q12 deletion syndrome MalaCards C3641756 Have diarrhea C2931189 Neural crest tumor MalaCards C4084802 Usual severity diarrhea C0017574 Gingivitis HSDN C0036572 Convulsion C1845050 Pigmentary disorder, reticulate, with systemic manifestations HPO C0018784 Deafness sensorineural C0024228 Lymphatic diseases HSDN C0010520 Skin cyanosis C0085277 Munchausen by proxy syndrome HSDN C0022660 Acute kidney failure C3536715 Aa amyloidosis MalaCards C0012833 Dizzy C0035302 Retinal artery occlusion HSDN C1549543 Administration method - pain C0032371 Poliomyelitis HSDN C0184567 Pain acute C0521168 Injuries occupational HSDN C1145670 Failure respiratory C0410179 Scleroatonic muscular dystrophy MalaCards C0008031 Pain chest C0006277 Bronchitis UMLS C0018784 Deafness sensorineural C0029396 Heterotopic ossification HSDN C0151786 Weakness muscle C0027439 Nasopharyngeal neoplasms HSDN C0476273 Distress respiratory C1855102 Methylmalonic aciduria cblb type HPO|UMLS C2237041 Shox gene with short stature C2675014 Mullerian aplasia and hyperandrogenism OrphaNet|HPO|MalaCards C1145670 Failure respiratory C2930852 Zellweger leukodystrophy MalaCards C0013604 Edematous C0035258 Restless legs syndrome HSDN C4085210 Usual severity pain C0024809 Marijuana abuse HSDN C2055125 Temperature reported over 102 degrees fahrenheit C0040584 Tracheitis DiseaseOntology C4084775 Usual severity weight loss C0001403 Addison disease OrphaNet|HSDN C0162298 Stiffness joints C4024961 Metachromatic leukodystrophy variant MalaCards C0037317 Sleep disturbance C0268225 Aspartylglucosaminuria MalaCards|HPO C1549543 Administration method - pain C0042384 Vasculitis HSDN C1961131 Cough adverse event C0014236 Endophthalmitis HSDN C4084784 Diarrhea C0079744 Diffuse large b-cell lymphoma HSDN C1069915 Vertigo C0007789 Cerebral palsy HSDN C0424755 Fever symptoms C0024118 Lung disease, parasitic HSDN C0022346 Yellow skin C0004238 Atrial fibrillation HSDN C0587050 Lower extremity mass C0042548 Plantar wart UMLS C4084727 Cough frequency C0019270 Hernia HSDN C4084724 Usual severity constipation C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C2025995 Cellulitis C0006666 Calciphylaxes OrphaNet|MalaCards C0018772 Deafness C1710146 Familial spinal arachnoiditis MalaCards C3463815 Feel fatigue C0034065 Pulmonary embolism HSDN C0344315 Mood depressed C3888138 Monosomy x MalaCards C2911647 Weight gain adverse event C0085298 Sudden cardiac death HSDN C0917816 Deficiency mental C2748572 Sesame syndrome HPO C2029884 Hearing loss by exam C0015663 Fasting HSDN C0000737 Abdomen pain C0007766 Intracranial aneurysm HSDN C0033377 Caudal displacement C2700265 Waardenburg syndrome type 2 HPO C4085211 Pain distress question C0042345 Varicosity HSDN C1963252 Tremor adverse event C1719788 Episodic ataxia type 1 HPO C4084768 Usual severity vomiting C0027947 Neutropenia HSDN C0033774 Skin pruritus C0023645 Lichen planus follicularis OrphaNet|MalaCards C4084774 Have weight loss C0027661 Neoplasms, hormone-dependent HSDN C4085661 Usual severity nausea C0043251 Wounds and injuries HSDN C0423715 Testicular neuralgia C1290837 Disease of trunk UMLS C0026826 High muscle tone C0796222 Mental retardation, x linked 16 MalaCards C0011991 Loose stools C0162557 Liver failure, acute HSDN C0009080 Finger clubbing C1275083 Hereditary sclerosing poikiloderma of weary MalaCards C4084784 Diarrhea C0027430 Nasal polyps HSDN C0018991 Paralysis one side of body C4082173 Porencephaly HSDN C3274924 Have been coughing C0001721 Emotional affect HSDN C0424755 Fever symptoms C0024312 Lymphopenia HSDN C4084784 Diarrhea C0042134 Uterine hemorrhage HSDN C0007758 Cerebellar ataxia C0520679 Sleep apnea, obstructive HSDN C0018524 Hallucinate C0751072 Frontotemporal lobar degeneration MalaCards C0232466 Feeding difficulty C3180937 15q11.2 microdeletion MalaCards C0030193 Sense of pain C1336344 Stage iva laryngeal verrucous carcinoma UMLS C0522224 Palsied C0015814 Femur head necrosis HSDN C0030193 Sense of pain C0600104 Obsessive compulsive behavior HSDN C2024893 Cardiovascular surgery result: fatigue C0038012 Spondylitis HSDN C0015230 Exanthem C0268680 Biotin deficiency MalaCards C0349506 Sun sensitivity C0342861 Uroporphyrinogen decarboxylase deficiency MalaCards C2919142 Short stature adverse event C0796208 Mental retardation, x-linked 3 HPO C3887638 Failure to thrive in infant C0027819 Neuroblastoma MalaCards C0460137 Push down or depress C0342859 Harderoporphyria HPO C0003469 Anxiety disorder C0271865 Autoimmune hypoparathyroidism MalaCards C0036659 Sensation disorder C0221065 Subacute combined degeneration HSDN C1963093 Dizziness adverse event C4049644 Depression HSDN C0007758 Cerebellar ataxia C0268151 Classical galactosemia MalaCards|HPO C0011991 Loose stools C0241932 X-linked hypogammaglobulinemia HPO C0004134 Dyssynergia C0025286 Meningioma MalaCards|HSDN C0037317 Sleep disturbance C0751664 Canavan disease, neonatal OrphaNet|HPO C0013604 Edematous C0002438 Amebiasis HSDN C0042571 Vertigo subjective C0149514 Bronchitis acute HSDN C0013604 Edematous C0013449 Ear neoplasms HSDN C0917816 Deficiency mental C0265373 Fetal trimethadione syndrome OrphaNet|MalaCards C0018681 Headache, cephalalgia C2609414 Acute kidney injury HSDN C3887638 Failure to thrive in infant C1837218 Cleft palate, isolated HSDN C2984058 Have pain C0023786 Mucopolysaccharidosis i HSDN C0027066 Myoclonic jerking C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome MalaCards C0034151 Hyperglobulinemic purpura C0085110 Severe combined immunodeficiency HSDN C4085211 Pain distress question C0221757 Alpha 1-antitrypsin deficiency HSDN C4085862 Bothered by nausea C0035066 Renal artery obstruction HSDN C1963086 Confusion adverse event C2936703 Familial kleine levin syndrome MalaCards C4084774 Have weight loss C0000833 Abscess HSDN C3665386 Abnormal vision C2931588 Gemss syndrome MalaCards C0033774 Skin pruritus C0853697 Neutrophil count decreased HSDN C4084768 Usual severity vomiting C0042164 Uveitis HSDN C0030552 Paralysis partial C0018213 Graves disease HSDN C0036572 Convulsion C1848070 Lissencephaly and agenesis of corpus callosum HPO C0042798 Vision dim C0265253 Stickler syndrome (disorder) OrphaNet C3649804 Change in elimination habits C2017951 Special symptoms or syndromes, not elsewhere classified in medcin UMLS C0152459 Striae C2028283 History of premature birth HSDN C0024031 Back pain lower back C0037199 Sinusitis HSDN C0020672 Body temperature decreased C0010674 Cystic fibrosis HSDN C3898969 Have been vomiting C0085278 Antiphospholipid syndrome HSDN C1963063 Anorexia adverse event C1963106 Esophagitis adverse event HSDN C0030193 Sense of pain C1956418 Torsion abnormality HSDN C0151786 Weakness muscle C0042830 Perception visual HSDN C0016204 Fart C0453996 Tobacco smoking HSDN C1963252 Tremor adverse event C0398746 Gluthathione synthetase deficiency MalaCards C4084774 Have weight loss C3469186 Hemochromatosis, type 1 HSDN C0018681 Headache, cephalalgia C0014511 Epithelial cyst HSDN C0022346 Yellow skin C4048826 Mud fever MalaCards C4084724 Usual severity constipation C2984289 Melanoma pathway HSDN C0030200 Intractable pain C4085311 Depression - recess HSDN C0349588 Stature short C0265514 Dermatofibrosis lenticularis disseminata OrphaNet|HPO|MalaCards C0013604 Edematous C0004610 Bacteremia HSDN C0426579 Anorexia symptom C0085293 Hepatitis e MalaCards C0857305 Thrombocytopenia purpura C0031036 Polyarteritis nodosa HSDN C0427068 Legs weakness C1846046 Spastic paraplegia 16, x-linked (disorder) MalaCards C1279888 Proteinuria of undiagnosed cause C0035801 Diseases rodent HSDN C0392702 Abnormal involuntary movement C1970238 Episodic kinesigenic dyskinesia 2 MalaCards C4085661 Usual severity nausea C3812171 Bradycardia by ecg finding HSDN C0026821 Cramp C0014859 Esophageal neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0032963 Pregnancy complications, cardiovascular HSDN C4084725 Usual severity cough C0043324 Juvenile xanthogranuloma HSDN C3463815 Feel fatigue C0748397 Reynolds syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0014858 Esophageal motility disorders HSDN C0027498 Nausea vomiting C1336537 Supratentorial meningioma MalaCards C0011991 Loose stools C1962986 Glaucoma adverse event HSDN C0242936 Center pain C0947622 Cholecystolithiasis HSDN C3665347 Vision impaired C0795956 Chylomicron retention disease MalaCards|HPO C4084775 Usual severity weight loss C0035869 Rotavirus infections HSDN C1963064 Anxiety adverse event C0220704 Shprintzen syndrome MalaCards|HPO C0030193 Sense of pain C0017924 Glycogen storage disease type v HSDN C3662832 Daytime hypersomnia C0917799 Hypersomnia UMLS C0013362 Dysarthrias C0027126 Myotonic dystrophy HSDN C0424755 Fever symptoms C0085293 Hepatitis e MalaCards C0034151 Hyperglobulinemic purpura C0001768 Agammaglobulinemia HSDN C0700078 Deep tendon reflex decrease C0007959 Charcot-marie-tooth disease HPO C0231218 Malaise generalized C0019360 Herpes zoster disease DiseaseOntology|MalaCards C1263846 Attention deficit disorder with hyperactivity C0152164 Cyclical vomiting syndrome (disorder) MalaCards C4084725 Usual severity cough C0037051 Behavior illness HSDN C0812426 Kidney problem C0748283 Renal cyst complex UMLS C0037383 Sneeze C0002949 Aneurysm, dissecting HSDN C3829611 Nausea frequency C3813607 Infantile gastroesophageal reflux HSDN C3665347 Vision impaired C0877075 Intraosseous angioma MalaCards C0018681 Headache, cephalalgia C0020492 Hyperostosis HSDN C0013604 Edematous C0040136 Thyroid neoplasm HSDN C0003910 Articulation disorder C0399526 Class iii malocclusion HSDN C1069915 Vertigo C0002726 Amyloidosis HSDN C0018777 Deafness, conductive C1261470 Congenital meningocele HSDN C2984058 Have pain C0022672 Acute kidney tubular necrosis HSDN C0018772 Deafness C0041316 Lymph node tuberculosis HSDN C1557397 Adverse event associated with pain C0751792 Trauma, nervous system HSDN C0040822 D tremors C0525045 Mood disorders HSDN C0003460 Anurias C0266313 Allanson pantzar mcleod syndrome MalaCards|HPO C0028738 Nystagmus C0268495 Oculocutaneous albinism type 2 OrphaNet|HPO|MalaCards C0349588 Stature short C1862170 Brachydactyly with hypertension OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0017661 Iga glomerulonephritis HSDN C2984058 Have pain C1963266 Uveitis adverse event HSDN C0015230 Exanthem C0041296 Tuberculosis UMLS C0242936 Center pain C0004031 Aspergillosis, allergic bronchopulmonary HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1306503 Congenital exomphalos HSDN C2911647 Weight gain adverse event C0034494 Rabies (disorder) HSDN C0000737 Abdomen pain C0022650 Kidney calculi HSDN C0018772 Deafness C0005974 Bone resorption HSDN C0027066 Myoclonic jerking C0001418 Adenocarcinoma HSDN C1963063 Anorexia adverse event C0376286 Avitaminosis HSDN C0003862 Pain joint C0027643 Neoplasm recurrence, local HSDN C0010200 Cough symptom C0751674 Lymphangioleiomyomatosis OrphaNet|HSDN|HPO|MalaCards C0010200 Cough symptom C0003493 Aortic diseases HSDN C0012833 Dizzy C0030286 Pancreatic diseases HSDN C0003113 Anomia C0751813 Chronic brain injury HSDN C0575081 Abnormal gait C2931347 Cardiac form of generalized glycogenosis MalaCards C1962956 Flatulence adverse event C0012242 Digestive system disorders HSDN C0012833 Dizzy C0011581 Depressive disorder HSDN C0018784 Deafness sensorineural C1866351 Peroxisome biogenesis disorder, complementation group 11 MalaCards C1963077 Bone pain adverse event C1418399 Pdb1 gene HPO C0018965 Blood urine C2873856 Essential cryoglobulinemia MalaCards C0030196 Limb pain C1860518 Vasculopathy, retinal, with cerebral leukodystrophy MalaCards|HPO C0036572 Convulsion C3494880 Convulsions in the newborn, non-refractory UMLS C0008031 Pain chest C2239253 Aneurysm of sinus of valsalva MalaCards C4085211 Pain distress question C0040961 Tricuspid valve insufficiency HSDN C0033377 Caudal displacement C0751267 Encephalopathy, subacute necrotizing, infantile MalaCards C0241210 Speaking delay C1845543 Mental retardation, x-linked, with epilepsy MalaCards|HPO C2911645 Weight loss adverse event C0751357 Focal myositides MalaCards C4084802 Usual severity diarrhea C0040809 Patient refusal of treatment HSDN C1384666 Decreased hearing C1864825 Frias syndrome MalaCards C4050613 Anxiety C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C0037317 Sleep disturbance C2931817 Chromosome 2q37 deletion syndrome MalaCards|HPO|UMLS C0030554 Abnormal sensation C0030578 Paronychia inflammation HSDN C0004134 Dyssynergia C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C1963137 Hydrocephalus adverse event C0599973 Waardenburg anophthalmia syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0161406 Injury nerve trigeminal HSDN C0042024 Urine incontinence C1846707 Spinocerebellar ataxia 17 MalaCards|HPO C0030193 Sense of pain C0013274 Patent ductus arteriosus HSDN C0349588 Stature short C0265216 X-linked hydrocephalus syndrome MalaCards C4085862 Bothered by nausea C0014121 Bacterial endocarditis HSDN C0043094 Weight gain C0004943 Behcet syndrome HSDN C3463815 Feel fatigue C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0043094 Weight gain C3541306 Plasmodium measurement HSDN C0000737 Abdomen pain C1333085 Colon carcinoma metastatic in the liver UMLS C4085211 Pain distress question C0031190 Persistent fetal circulation syndrome HSDN C0012833 Dizzy C0015414 Eye neoplasms HSDN C0005745 Blepharoptosis C1864825 Frias syndrome MalaCards C4085210 Usual severity pain C0032371 Poliomyelitis HSDN C0036572 Convulsion C1963139 Hypopigmentation adverse event HSDN C0860603 Anxiety symptom C1865926 Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) MalaCards C0333243 Edema pitting C0268382 Amyloid nephropathy MalaCards C0037317 Sleep disturbance C2678194 Mental retardation, x-linked, syndromic, christianson type HPO|UMLS C0020538 Hbp C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C0027796 Neuralgias C0022758 Kap HSDN C4084767 Bothered by vomiting C0085096 Peripheral vascular diseases HSDN C0242936 Center pain C0009763 Conjunctivitis HSDN C1557397 Adverse event associated with pain C0006262 Bronchial fistula HSDN C4085317 Diarrhea frequency C0334533 Arteriovenous hemangioma HSDN C0019572 Hairiness C0265306 Greig cephalopolysyndactyly syndrome MalaCards|HPO C0234146 Absent reflex C0574085 3-methylglutaconic aciduria type 4 MalaCards C0022346 Yellow skin C0038160 Staphylococcal infections HSDN C1961131 Cough adverse event C0038663 Suicide attempt HSDN C0011570 Monopolar depression C0751208 Juvenile huntington disease MalaCards C1962972 Proteinuria adverse event C1864997 Majeed syndrome MalaCards|HPO C0034933 Abnormal reflexes C0033845 Pseudotumor cerebri HSDN C1963064 Anxiety adverse event C0268632 Homocarnosinosis MalaCards C0013428 Painful urination C0024535 Malaria, falciparum HSDN C0012833 Dizzy C0339784 Rubella endocochlear UMLS C0522224 Palsied C0034931 Reflex sympathetic dystrophy HSDN C0019825 Voice hoarseness C0015458 Facial hemiatrophy HSDN C0042928 Paralysis vocal cord C0018800 Cardiomegaly HSDN C0037771 Paraparesis spastic C0220994 Hyperammonemia HSDN C0022346 Yellow skin C2064409 Intrahepatic bile duct cystadenocarcinoma UMLS C1962956 Flatulence adverse event C0020701 Somatization disorder HSDN C0041105 Jaw spasm C1704421 Skin pigmentation disorder HSDN C0004604 Pain back C0009324 Ulcerative colitis HSDN C0020538 Hbp C3854315 Pseudoprimary hyperaldosteronism MalaCards C0231528 Muscle pain generalized C2347126 Microscopic polyarteritis MalaCards C3146279 Coma C0221021 Microangiopathic hemolytic anemia MalaCards C1069915 Vertigo C0033578 Prostatic neoplasms HSDN C0424755 Fever symptoms C0039128 Syphilis HSDN C0004604 Pain back C0001418 Adenocarcinoma HSDN C0013404 Respiratory difficulty C4084909 Depression subordinate domain HSDN C0042963 Symptoms vomiting C2936913 Porphyria, south african type HPO C1549543 Administration method - pain C0242966 Systemic inflammatory response syndrome HSDN C0009806 Constipate C0018790 Cardiac arrest HSDN C0242936 Center pain C0038325 Stevens-johnson syndrome HSDN C3539022 Pelvic pain decreasing in severity C0035358 Retroperitoneal neoplasm HSDN C0042963 Symptoms vomiting C0008350 Cholelithiasis HSDN C0426579 Anorexia symptom C0153459 Malignant neoplasm of body of pancreas MalaCards C0015970 Fever unknown origin C0016397 Focal infection HSDN C2032395 Pelvic pain on the left C0020517 Hypersensitivity HSDN C0032227 Effusion pleural C0085083 Ovarian hyperstimulation syndrome OrphaNet|HPO|MalaCards C4084725 Usual severity cough C0041466 Typhoid fever MalaCards C4085661 Usual severity nausea C0376545 Hematologic neoplasms HSDN C1384666 Decreased hearing C0024314 Lymphoproliferative disorders HSDN C0018784 Deafness sensorineural C1845446 Corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia OrphaNet|HPO C1279888 Proteinuria of undiagnosed cause C0020541 Hypertension, portal HSDN C0577569 Mass of male genital structure C2959569 Median raphe cyst of penis UMLS C0040822 D tremors C1851443 Cerebrooculofacioskeletal syndrome 3 HPO C0231791 In toe C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C1963184 Nystagmus adverse event C1846278 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (disorder) OrphaNet C0030486 Extremity paralysis, lower C4042784 Feeding and eating disorders HSDN C0018681 Headache, cephalalgia C0023283 Leishmaniasis, cutaneous HSDN C0013144 Drowsy C0033922 Psychomotor disorders MalaCards C4084775 Usual severity weight loss C0221036 Acrodermatitis enteropathica HPO C0030486 Extremity paralysis, lower C0038454 Cerebrovascular accident HSDN C4084725 Usual severity cough C0027429 Nasal obstruction present finding HSDN C0018777 Deafness, conductive C0028326 Noonan syndrome HSDN C0026603 Motion sickness C0022758 Kap HSDN C0040264 Ear ringing sound C0042568 Vertebrobasilar insufficiency HSDN C1557397 Adverse event associated with pain C0035204 Respiration disorders HSDN C4084774 Have weight loss C1868649 Panic disorder 1 HSDN C0017181 Gastrointestinal bleed C3495801 Granulomatosis with polyangiitis MalaCards|HPO C0003811 Cardiac rhythm disturbance C0003499 Supravalvular aortic stenosis OrphaNet|HPO C0028738 Nystagmus C0376524 Branchio-oculo-facial syndrome MalaCards|HPO C4085548 Usual severity dizziness C0036341 Schizophrenia HSDN C0015672 Decreased energy C0042510 Ventricular fibrillation HSDN C3541349 Syncope C0305062 Tetanus toxoids HSDN C1549543 Administration method - pain C0242350 Erectile dysfunction HSDN C0000737 Abdomen pain C0005591 Avian disease HSDN C0240715 Perineal lump C0686135 Neoplasm of uncertain behavior of the perineum, nos UMLS C0019209 Large liver C3150802 Myopathy, lactic acidosis, and sideroblastic anemia 2 MalaCards|HPO C0015672 Decreased energy C0162809 Kallmann syndrome HPO C4084725 Usual severity cough C3203727 Pneumorrhachi HSDN C0151786 Weakness muscle C0264766 Rheumatic mitral stenosis HSDN C0018681 Headache, cephalalgia C0029417 Osteoblastoma HSDN C0751837 Gait ataxic C0002880 Autoimmune hemolytic anemia HSDN C0162429 Dietary deficiency C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C0008031 Pain chest C3658239 D personality, type HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0854906 Benign schwannoma MalaCards C0020615 Hypoglycemia nos C1856405 Glutaric aciduria iic HPO C0013604 Edematous C0597109 Nurse's role HSDN C2315100 Pediatric failure to thrive C2749862 Mitochondrial neurogastrointestinal encephalopathy syndrome, rrm2b-related HPO C4085862 Bothered by nausea C0162739 Hellp syndrome HSDN C1963249 Tinnitus adverse event C0597109 Nurse's role HSDN C0424755 Fever symptoms C0005974 Bone resorption HSDN C4084784 Diarrhea C1522057 Acute enteritis of the mouse intestinal tract HSDN C0013456 Pain ear C1333989 Familial meningioma MalaCards C0037317 Sleep disturbance C1578691 Congenital myxedema MalaCards C4084768 Usual severity vomiting C0009404 Colorectal neoplasms HSDN C1963281 Vomiting adverse event C0040799 Traumatic subcutaneous emphysema HSDN C1962972 Proteinuria adverse event C0016658 Fracture bone HSDN C1963091 Diarrhea adverse event C2931002 Congenital disorder of glycosylation type 1h MalaCards C1963274 Vasculitis adverse event C2931916 Midline granulomatosis MalaCards C0042571 Vertigo subjective C0314657 Genetic predisposition HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041312 Tuberculosis git nos HSDN C3641755 Have constipation C0041466 Typhoid fever MalaCards|HSDN C0233565 Bradykinesia C1866770 Spinocerebellar ataxia with rigidity and peripheral neuropathy UMLS C0030232 Color loss C2931850 Aase smith syndrome 2 OrphaNet|HPO|MalaCards C1963063 Anorexia adverse event C0022758 Kap HSDN C3539892 Pelvic pain in front C0027095 Myosarcoma HSDN C0000737 Abdomen pain C3266155 Functional abdominal pain syndrome UMLS C0497406 Over weight C0020523 Immediate hypersensitivity HSDN C3463815 Feel fatigue C0948264 Neuroborreliosis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0027720 Nephrosis HSDN C0018681 Headache, cephalalgia C0025281 Meniere disease HSDN C0038002 Spleen enlargement C0004943 Behcet syndrome MalaCards|HPO C0020578 Hyperventilate C0037397 Behavior social HSDN C0042963 Symptoms vomiting C0038579 Substance abuse, intravenous HSDN C2220035 Persistent bulging of eyes C0015300 Exophthalmos UMLS C3641756 Have diarrhea C0022373 Disease, jejunal HSDN C0012833 Dizzy C0023448 Lymphoid leukemia HSDN C0037383 Sneeze C1306759 Eosinophilic disorder HSDN C2096293 Ent surgical result ear vertigo C0458220 Nervus intermedius neuralgia MalaCards C0027066 Myoclonic jerking C0038356 Stomach neoplasms HSDN C1963091 Diarrhea adverse event C0349231 Phobic anxiety disorder HSDN C0917816 Deficiency mental C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C0018926 Emesis bloody C0236969 Substance-related disorders HSDN C0221752 Rbc urine C0543697 Mixed cryoglobulinemia OrphaNet|MalaCards C2911645 Weight loss adverse event C3273031 Hnec MalaCards C0018808 Murmur C0344423 Atrial flutter by ecg finding HSDN C0023012 Delay language C2673873 Bardet-biedl syndrome 13 HPO C4084784 Diarrhea C0242698 Ventricular dysfunction, left HSDN C1069915 Vertigo C0017563 Gingival diseases HSDN C0036572 Convulsion C0011175 Dehydration HSDN C1557397 Adverse event associated with pain C0010631 Cystadenocarcinoma HSDN C0034150 Skin purpura C0342443 Adrenal cushing's syndrome MalaCards C0232462 Appetite decrease C0345904 Malignant neoplasm of liver MalaCards C0575081 Abnormal gait C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0000737 Abdomen pain C0398625 Protein c deficiency HSDN C3898969 Have been vomiting C0011303 Demyelinating diseases HSDN C0010520 Skin cyanosis C0040124 Thyroglossal duct cyst HSDN C4084766 Vomiting C0024788 Green monkey virus disease DiseaseOntology|MalaCards C2911647 Weight gain adverse event C1135821 Mortality syndrome, spiking HSDN C2984058 Have pain C0010035 Hereditary corneal dystrophy HSDN C0497247 Blood pressure elevation C0346302 Growth hormone-secreting pituitary adenoma HPO C0557874 Global developmental delay C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0026838 Spasticity muscle C0268386 Amyloid polyneuropathy, swiss type MalaCards C0012833 Dizzy C0013370 Amebic colitis HSDN C0018784 Deafness sensorineural C0003469 Anxiety disorders HSDN C2242996 Tingling C0030472 Paraneoplastic syndromes HSDN C0039070 Collapse fleeting C0878544 Cardiomyopathies UMLS C0009421 Comatose C0524910 Hepatitis c, chronic HSDN C3641756 Have diarrhea C0003650 Apudoma HSDN C0518090 Frequency of pain question C0031762 Photosensitivity disorders HSDN C2024893 Cardiovascular surgery result: fatigue C0221023 Cyclic neutropenia OrphaNet|HPO C0851578 Disorder sleep C0517555 Venous thrombosis after immobility HSDN C0042755 Virilisation C0022658 Kidney diseases HSDN C0010200 Cough symptom C0008628 Chromosome deletion HSDN C2984057 Have nausea C4041080 Neurocognitive disorders HSDN C1963247 Ventricular tachycardia adverse event C1969081 Arrhythmogenic right ventricular dysplasia, familial, 12 HPO C1963252 Tremor adverse event C0014060 Encephalitis, st. louis HSDN C4085211 Pain distress question C2827407 Infectious otitis media HSDN C0000727 Abdomen acute C0037054 Sickle cell trait HSDN C0011991 Loose stools C0027726 Nephrotic syndrome HSDN C1963091 Diarrhea adverse event C0007762 Cerebellar neoplasms HSDN C4084802 Usual severity diarrhea C0031142 Peritoneal diseases HSDN C0037771 Paraparesis spastic C0027873 Neuromyelitis optica HSDN C0011206 Delirium acute C0011269 Dementia, vascular HSDN C0013404 Respiratory difficulty C0034065 Pulmonary embolism UMLS C0024032 Birth weight subnormal C3468041 Fanconi anemia, complementation group c MalaCards C0009806 Constipate C0014170 Endometrial neoplasms HSDN C4085549 Dizziness C0019372 Herpesviridae infections HSDN C1963087 Constipation adverse event C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0018681 Headache, cephalalgia C0019080 Hemorrhage HSDN C0002622 Amnesias C2063866 Depressive disorder, treatment-resistant HSDN C0009421 Comatose C0263390 Papular mucinosis HSDN C0027497 Queasy C0027051 Myocardial infarction HSDN C0042928 Paralysis vocal cord C0175702 Williams syndrome MalaCards|HPO C0751495 Seizure focal C0238111 Lennox-gastaut syndrome MalaCards|HPO C4084726 Distress cough C0014175 Endometriosis HSDN C2032396 Pelvic pain on the right C0026857 Musculoskeletal diseases HSDN C0037317 Sleep disturbance C0037320 Night terrors UMLS C0851578 Disorder sleep C1090821 Sepsis (invertebrate) HSDN C0242936 Center pain C0376547 Aromatherapy HSDN C1963086 Confusion adverse event C0028768 Obsessive-compulsive disorder HSDN C0042963 Symptoms vomiting C0238417 Scorpion sting HSDN C4085549 Dizziness C0020179 Huntington disease HSDN C0085602 Polydypsia C0033968 Psychotherapeutic technique HSDN C0031315 Phantom limb pain C0037650 Somatoform disorder HSDN C1549543 Administration method - pain C0039106 Pigmented villonodular synovitis HSDN C0242936 Center pain C0600040 Chronic interstitial cystitis OrphaNet C0036572 Convulsion C0042133 Uterine fibroids HSDN C0030552 Paralysis partial C0035334 Retinitis pigmentosa HSDN C4085661 Usual severity nausea C1962979 Burn adverse event HSDN C2911647 Weight gain adverse event C0027697 Nephritis HSDN C1963281 Vomiting adverse event C0033054 Prenatal exposure delayed effects HSDN C1549543 Administration method - pain C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C1069915 Vertigo C3244301 Coverage level - family HSDN C0036572 Convulsion C0038002 Splenomegaly HSDN C3665346 Loss sight C1840452 Hyaloideoretinal degeneration of wagner HPO C0151786 Weakness muscle C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C4084776 Weight loss C0021400 Influenza HSDN C2024893 Cardiovascular surgery result: fatigue C0687150 Parathyroid gland adenocarcinoma OrphaNet|HPO|MalaCards C4084776 Weight loss C0042131 Uterine diseases HSDN C0560024 Eyelid swelling C0268074 Indian childhood cirrhosis MalaCards C3203358 Alveolar hypoventilation C0234421 Conscious HSDN C0013362 Dysarthrias C3553719 Amyotrophic lateral sclerosis 18 MalaCards C0812426 Kidney problem C0748302 Renal failure chronic hypertension UMLS C1963071 Back pain adverse event C1720777 Functional laterality HSDN C4085862 Bothered by nausea C0042594 Vestibular diseases HSDN C0018681 Headache, cephalalgia C2118142 Dialysis headache UMLS C0221752 Rbc urine C0340992 Cryoglobulinemic; vasculitis OrphaNet|MalaCards C0037384 Snore C0014394 Enuresis HSDN C0011991 Loose stools C0025063 Mediastinal neoplasms HSDN C4085210 Usual severity pain C0033941 Psychoses, substance-induced HSDN C1963170 Hypothermia adverse event C0085073 Prosthesis-related infection HSDN C0002962 Angina C0024790 Paroxysmal nocturnal hemoglobinuria MalaCards|HPO C1963091 Diarrhea adverse event C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C2237041 Shox gene with short stature C1836315 Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia MalaCards C0020538 Hbp C1859728 Coronary sclerosis, medial, of infancy HPO C0026821 Cramp C1963134 Hemorrhoids adverse event HSDN C2919142 Short stature adverse event C3150928 Nf1 microdeletion syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C0239981 Hypoalbuminemia HSDN C2919142 Short stature adverse event C2930971 Acroosteolysis dominant type OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0003431 Antisocial personality disorder HSDN C3641756 Have diarrhea C0024899 Mastocytosis OrphaNet|MalaCards C0036659 Sensation disorder C0019360 Herpes zoster disease HSDN C3887638 Failure to thrive in infant C0282102 Chondrodysplasia punctata, x-linked dominant type HPO C4084726 Distress cough C0007766 Intracranial aneurysm HSDN C4042891 Sleep wake disorders C0042075 Urologic diseases HSDN C0030486 Extremity paralysis, lower C0007131 Non-small cell lung carcinoma HSDN C0723402 Sore throat C0032371 Poliomyelitis MalaCards C0036572 Convulsion C1550672 Specimen type - ulcer HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030354 Papilloma HSDN C0575081 Abnormal gait C0087012 Ataxia, spinocerebellar MalaCards C4084776 Weight loss C0262627 Seroma HSDN C0024031 Back pain lower back C0432264 Axial osteosclerosis MalaCards C3898969 Have been vomiting C0004275 Attitude health HSDN C4084767 Bothered by vomiting C0017416 Genital neoplasms, female HSDN C0010200 Cough symptom C0005940 Bone diseases HSDN C0012833 Dizzy C0032344 Poisoning aspects HSDN C1963086 Confusion adverse event C0004943 Behcet syndrome OrphaNet|HPO|MalaCards C0221752 Rbc urine C0268448 Primary hypomagnesemia (disorder) MalaCards|HPO C0022346 Yellow skin C0026650 Movement disorders HSDN C0497406 Over weight C0080179 Vertebra fracture HSDN C4084725 Usual severity cough C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0221166 Paraparesis C0007350 Cat disease HSDN C0557874 Global developmental delay C3554385 Congenital disorder of glycosylation, type iu MalaCards C1000483 Genus anemia C0206641 Osteochondromatosis MalaCards C1963281 Vomiting adverse event C0268680 Biotin deficiency MalaCards C3665347 Vision impaired C2931291 Familial spastic paraparesis and deafness OrphaNet|MalaCards C3665347 Vision impaired C1852438 Cataract, coppock-like MalaCards|HPO C0036572 Convulsion C0035321 Retinal tear HSDN C2032395 Pelvic pain on the left C0438692 Vaginal discharge symptom HSDN C0009806 Constipate C1275081 Cardio-facio-cutaneous syndrome HPO|UMLS C1963274 Vasculitis adverse event C0001733 Afibrinogenemia HPO C0018777 Deafness, conductive C0175695 Sotos' syndrome OrphaNet|HSDN|HPO|MalaCards C0518090 Frequency of pain question C0014849 Esophageal and gastric varices HSDN C1549543 Administration method - pain C0032964 Pregnancy complications, hematologic HSDN C0151311 Cranial nerve palsy C1854336 Paragangliomas 3 MalaCards C4085661 Usual severity nausea C1265748 Torsion HSDN C0424755 Fever symptoms C0040558 Toxoplasmosis DiseaseOntology|HSDN C2024893 Cardiovascular surgery result: fatigue C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0000727 Abdomen acute C0017160 Gastroenteritis HSDN C2096293 Ent surgical result ear vertigo C0001883 Airway obstruction HSDN C0000737 Abdomen pain C0010346 Crohn disease MalaCards|UMLS C1549543 Administration method - pain C0242550 Behavior, risk reduction HSDN C0020672 Body temperature decreased C1706377 Memory device component HSDN C0036572 Convulsion C3536567 Idiopathic generalized epilepsy, non-intractable UMLS C1963091 Diarrhea adverse event C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0240608 Osler node C0162627 Skin diseases, bacterial UMLS C0497247 Blood pressure elevation C0044707 11 beta hsd HPO C4084726 Distress cough C0018939 Hematological disease HSDN C1963091 Diarrhea adverse event C0007682 Cns disorder HSDN C0242936 Center pain C1136154 Dysfunction, tibialis posterior HSDN C0151889 Reflexes tendon increased C1846278 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (disorder) OrphaNet C3829611 Nausea frequency C0024636 Malocclusion HSDN C0013428 Painful urination C0042063 Urogenital abnormalities HSDN C0004604 Pain back C0014848 Esophageal achalasia HSDN C0424755 Fever symptoms C0036864 Sexual relations HSDN C0037763 Spasm C0013418 Abnormal labor HSDN C0038990 Sweats C0017671 Glomus jugulare tumor HPO C2984058 Have pain C0024689 Mandibular diseases HSDN C0032285 Pneum C2936664 Acquired hypogammaglobulinemia MalaCards C0018772 Deafness C0023220 Leg injury HSDN C0020505 Excessive eating C0022658 Kidney diseases HSDN C0036572 Convulsion C0015944 Fetal membranes, premature rupture HSDN C0428977 Pulse rate decrease C3280692 Mchccd MalaCards C4084802 Usual severity diarrhea C0001580 Adolescent behavior HSDN C3887638 Failure to thrive in infant C3266101 22q11 partial monosomy syndrome HPO C4085211 Pain distress question C0016398 Focal infection, dental HSDN C0034933 Abnormal reflexes C0025312 Meningomyelocele HSDN C1962972 Proteinuria adverse event C3149711 Pheochromocytoma, susceptibility to HPO C4085211 Pain distress question C0018923 Hemangiosarcoma HSDN C0042964 Anticipatory vomiting C0038356 Stomach neoplasms HSDN C4084767 Bothered by vomiting C0027583 Nematode infections HSDN C3815497 Cough C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0221752 Rbc urine C0010691 Cystinuria OrphaNet|MalaCards C0007758 Cerebellar ataxia C0023890 Liver cirrhosis HSDN C0518090 Frequency of pain question C0013295 Duodenal ulcer HSDN C2024878 Cardiovascular surgery result: dyspnea C1956258 Familial thrombotic thrombocytopenic purpura MalaCards C0012569 Double vision C0030305 Pancreatitis HSDN C2919142 Short stature adverse event C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C0010034 Corneal diseases HSDN C0039231 Heartbeats increased C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0015970 Fever unknown origin C0205788 Histiocytoid hemangioma HSDN C0020673 Hypothermia (central) (local) C1547046 Kind of quantity - taste HSDN C0020305 Fetal edema C0019045 Hemoglobinopathies HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0279628 Adenocarcinoma of esophagus OrphaNet C2024878 Cardiovascular surgery result: dyspnea C0085183 Neoplasms, second primary HSDN C0221785 Wrist arthralgia C2674705 Osteolysis, hereditary, of carpal bones with or without nephropathy MalaCards|UMLS C1557397 Adverse event associated with pain C0037942 Spinal osteophytosis HSDN C0751401 Ophthalmoparesis C1837122 Myasthenic syndrome, congenital, fast-channel MalaCards|HPO C0009398 Color vision defects C0003708 Arachnitis HSDN C0030193 Sense of pain C0004576 Babesiosis HSDN C1069915 Vertigo C0018916 Hemangioma HSDN C1963086 Confusion adverse event C0749095 Subdural hematoma chronic HSDN C3815497 Cough C0028242 Nocardia infections HSDN C0149793 Transient monocular blindness C0162533 Porphyrias, hepatic HSDN C0012833 Dizzy C0395925 Hyperactive labyrinth UMLS C0557874 Global developmental delay C3554656 Dyskeratosis congenita, autosomal recessive 5 MalaCards C0003862 Pain joint C1258104 Diffuse scleroderma HSDN C3887784 Decreased urine output C0036690 Septicemia HSDN C4085222 Nausea C0154723 Migraine with aura HSDN C0030193 Sense of pain C0019021 Hemoglobin c disease HSDN C0018926 Emesis bloody C0022374 Jejunal neoplasms HSDN C1963093 Dizziness adverse event C0524910 Hepatitis c, chronic HSDN C0030794 Pelvis pain C2936631 Complaint, subjective health HSDN C0020672 Body temperature decreased C0033817 Pseudomonas infections HSDN C2024878 Cardiovascular surgery result: dyspnea C0043251 Wounds and injuries HSDN C3641756 Have diarrhea C0010034 Corneal diseases HSDN C0043094 Weight gain C2827407 Infectious otitis media HSDN C1384666 Decreased hearing C0751667 Canavan disease, juvenile MalaCards C3274924 Have been coughing C0494491 Mononeuropathies HSDN C2024893 Cardiovascular surgery result: fatigue C0038358 Gastric ulcer HSDN C0040034 Thrombocytopenia C0342731 Deficiency of mevalonate kinase MalaCards C4085862 Bothered by nausea C2945560 Hemolytic HSDN C0020903 Illusion C0036341 Schizophrenia HSDN C3898969 Have been vomiting C0016542 Foreign body HSDN C3665347 Vision impaired C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0009373 Colonic diseases HSDN C0030486 Extremity paralysis, lower C0152276 Granulocytic sarcoma HSDN C0018772 Deafness C0041327 Tuberculosis, pulmonary HSDN C0012569 Double vision C0751291 Desmoplastic medulloblastoma MalaCards C0750937 Appendicular ataxia C1861736 Spinocerebellar ataxia 31 (disorder) HPO C0018784 Deafness sensorineural C0021818 Intervertebral disk displacement HSDN C0027796 Neuralgias C0010068 Coronary heart disease HSDN C0019559 Hip arthralgia C2702825 Compression arthralgia of right pelvis, hip, or femor UMLS C0917816 Deficiency mental C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C0241210 Speaking delay C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards C0018991 Paralysis one side of body C1837218 Cleft palate, isolated HSDN C0413252 Hypothermia due to exposure C0019829 Hodgkin disease HSDN C1963087 Constipation adverse event C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C4084788 Have dizziness C0243026 Sepsis HSDN C0015230 Exanthem C0749684 Trichlormethiazide allergy UMLS C0011206 Delirium acute C0034885 Rectal neoplasms HSDN C0263540 Nail loss C1864826 Epidermolysis bullosa, lethal acantholytic MalaCards|UMLS C3887638 Failure to thrive in infant C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C0005745 Blepharoptosis C1850792 Congenital myasthenic syndrome ib MalaCards|HPO C4085317 Diarrhea frequency C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0020903 Illusion C0086543 Cataract nos HSDN C1963091 Diarrhea adverse event C0012546 Diphtheria HSDN C0497406 Over weight C0007282 Carotid stenosis HSDN C0013362 Dysarthrias C0750929 Arnold-chiari malformation, type i MalaCards C0013604 Edematous C0029422 Osteochondrodysplasias HSDN C0036572 Convulsion C3711390 9q22 deletion syndrome OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0016085 Filariasis HSDN C1963184 Nystagmus adverse event C0268506 Albinoidism MalaCards C2315100 Pediatric failure to thrive C1274233 T-lymphocyte immunodeficiency MalaCards C0015672 Decreased energy C0410422 Chronic multifocal osteomyelitis OrphaNet|MalaCards C0013404 Respiratory difficulty C0001127 Acidosis, respiratory UMLS C0018772 Deafness C1859569 Bardet-biedl syndrome 11 HPO C3541349 Syncope C0038358 Gastric ulcer HSDN C0037771 Paraparesis spastic C0038019 Spondylosis HSDN C0013404 Respiratory difficulty C1709580 Pleural well differentiated papillary mesothelioma UMLS C4084766 Vomiting C0024143 Lupus nephritis HSDN C0013390 Cramps menstrual C4085311 Depression - recess HSDN C2984057 Have nausea C0162871 Aortic aneurysm, abdominal HSDN C0040822 D tremors C1258104 Diffuse scleroderma HSDN C3274924 Have been coughing C0524688 Pneumonic plague DiseaseOntology|MalaCards C0015672 Decreased energy C0264939 Systemic vasculitis HSDN C4084792 Usual severity hair loss C1851970 Dyskeratosis congenita, autosomal dominant MalaCards C2911647 Weight gain adverse event C1963138 Hypertension adverse event HSDN C0011991 Loose stools C0033906 Psychological theories HSDN C3539892 Pelvic pain in front C0085096 Peripheral vascular diseases HSDN C0151889 Reflexes tendon increased C3150998 Spinocerebellar ataxia, autosomal recessive 10 MalaCards|HPO C4084774 Have weight loss C0012644 Animal disease models HSDN C2911647 Weight gain adverse event C0233629 Thinking and speaking disturbances HSDN C0242936 Center pain C0009447 Common variable immunodeficiency HSDN C0030193 Sense of pain C1299440 Angina recurrent status post directional coronary atherectomy UMLS C0009792 Consciousness disorder C0025289 Meningitis HSDN C0003910 Articulation disorder C0085094 Head injury closed HSDN C4085210 Usual severity pain C0040422 Tonsillar neoplasms HSDN C0028738 Nystagmus C3810080 Mental retardation, autosomal recessive 40 MalaCards C4084784 Diarrhea C0011880 Diabetic ketoacidosis HSDN C2984058 Have pain C0030499 Parasitic diseases HSDN C4084802 Usual severity diarrhea C0024117 Chronic obstructive airway disease HSDN C0085593 Chill C0152937 Primary pneumonic plague DiseaseOntology|MalaCards C3203358 Alveolar hypoventilation C2586211 Thrombosis of blood vessel HSDN C0013608 Cardiac edema C0027651 Tumor HSDN C4020887 Photodysphoria C0043397 Yellow fever, jungle MalaCards C1279888 Proteinuria of undiagnosed cause C0085096 Peripheral vascular diseases HSDN C0398650 Idiopathic thrombocytopenia purpura C0919267 Ovarian neoplasm HSDN C0232498 Abdominal tenderness C0267400 Acute haemorrhagic enterocolitis UMLS C0020538 Hbp C0162359 Christ-siemens-touraine syndrome MalaCards|HPO C3829611 Nausea frequency C1306577 Dies patient HSDN C0085593 Chill C0033375 Prolactinoma HSDN C0024031 Back pain lower back C0458225 Lumbar facet syndrome UMLS C0026205 Pupillary constriction C1418479 Pex7 gene HSDN C3641756 Have diarrhea C0025286 Meningioma HSDN C0042963 Symptoms vomiting C0035361 Pneumoretroperitoneum HSDN C2237041 Shox gene with short stature C0004775 Bartter disease OrphaNet|MalaCards C0878709 Cloudy (hemodialysis) (peritoneal) dialysis effluent C0042075 Urologic diseases UMLS C0019079 Bloody sputum C1708653 Laryngeal lymphoepithelial carcinoma UMLS C4084788 Have dizziness C0041582 Ulcer HSDN C0424755 Fever symptoms C0033348 Language program HSDN C0518090 Frequency of pain question C0022602 Actinic keratosis HSDN C3898969 Have been vomiting C0149931 Migraine disorders MalaCards C0007398 Catatonic C0013870 Electroconvulsive shock HSDN C0002962 Angina C2609414 Acute kidney injury HSDN C4085862 Bothered by nausea C0079774 Peripheral t-cell lymphoma HSDN C0236065 Edema mouth C1304478 Lymphedema of lip UMLS C0700078 Deep tendon reflex decrease C0342613 Danish type familial amyloid cardiomyopathy MalaCards C3641756 Have diarrhea C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C0039070 Collapse fleeting C0038579 Substance abuse, intravenous HSDN C0010520 Skin cyanosis C0265808 Cyanotic congenital heart disease UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0524909 Hepatitis b, chronic MalaCards|HSDN C0030552 Paralysis partial C1837454 Spinocerebellar ataxia 8 MalaCards C3815497 Cough C0025007 Measles DiseaseOntology|HSDN|MalaCards C0033377 Caudal displacement C0033922 Psychomotor disorders MalaCards C0030552 Paralysis partial C0009651 Conditioning operant HSDN C0036572 Convulsion C3887532 Ulceration HSDN C4042891 Sleep wake disorders C0033348 Language program HSDN C4084776 Weight loss C3714580 Hypokalemic periodic paralysis type 1 HSDN C3541349 Syncope C0018021 Goiter HSDN C3463815 Feel fatigue C0563150 Catastrophization HSDN C0019079 Bloody sputum C0854993 Lung squamous cell carcinoma stage iii UMLS C4084773 Bothered by weight gain C1136321 Hiv-associated lipodystrophy syndrome HSDN C0008031 Pain chest C0242707 Ventricular dysfunction, right HSDN C0024031 Back pain lower back C0018965 Hematuria HSDN C3887873 Hearing loss C4048196 Beta-mannosidosis HSDN C0231835 Respiration rate increased C0040433 Tooth crowding HSDN C0917816 Deficiency mental C0796237 Mental retardation, x-linked 30 HPO C2919142 Short stature adverse event C2677299 Cerebroretinal microangiopathy with calcifications and cysts (disorder) HPO C4084768 Usual severity vomiting C0032963 Pregnancy complications, cardiovascular HSDN C3539896 Pelvic pain occurs with urination C0432264 Axial osteosclerosis MalaCards C0012569 Double vision C0020517 Hypersensitivity HSDN C4084802 Usual severity diarrhea C0014511 Epithelial cyst HSDN C4084784 Diarrhea C0014761 Erythroblastosis, fetal HSDN C0018784 Deafness sensorineural C0005941 Bone diseases, developmental HSDN C0398650 Idiopathic thrombocytopenia purpura C0023521 Globoid cell leukodystrophy HPO C0020438 Hypercalciuria C2931121 Meier blumberg imahorn syndrome MalaCards C0022346 Yellow skin C0162568 Erythropoietic protoporphyria HSDN C1962972 Proteinuria adverse event C0036982 Shock, hemorrhagic HSDN C0030193 Sense of pain C0729346 Osteochondritis juvenilis HSDN C1860844 Sparse, thin hair C0795940 Filippi syndrome MalaCards|HPO C4085661 Usual severity nausea C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0518090 Frequency of pain question C0017185 Gastrointestinal neoplasms HSDN C2024878 Cardiovascular surgery result: dyspnea C0024421 Macroglossia HSDN C4085549 Dizziness C0028758 Bonding HSDN C0522224 Palsied C0014859 Esophageal neoplasms HSDN C0152459 Striae C0220679 Ehlers-danlos syndrome, autosomal dominant, type unspecified OrphaNet C4085549 Dizziness C0002395 Alzheimer's disease HSDN C0231678 Ulnar deviation of the wrists C0086651 Mucopolysaccharidosis, mps-iv-a HPO|UMLS C1549543 Administration method - pain C0042345 Varicosity HSDN C0018681 Headache, cephalalgia C0036439 Scoliosis, unspecified HSDN C0042571 Vertigo subjective C1962963 Osteoporosis adverse event HSDN C3898969 Have been vomiting C1963229 Retinal detachment adverse event HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004610 Bacteremia HSDN C2984058 Have pain C0032064 Plague HSDN C0009792 Consciousness disorder C1412004 Tumor of the pineal region HSDN C0424755 Fever symptoms C0275982 Campylobacter enteritis MalaCards C0015230 Exanthem C0020517 Hypersensitivity UMLS C4084784 Diarrhea C0000809 Abortion, habitual HSDN C0034155 Thrombotic thrombocytopenic purpura C0040136 Thyroid neoplasm HSDN C4084802 Usual severity diarrhea C2749602 Autoimmune polyendocrinopathy syndrome, type i, with reversible metaphyseal dysplasia HPO C0009806 Constipate C0002940 Aneurysm HSDN C0042420 Vasovagal episode C0004238 Atrial fibrillation HSDN C0020455 Hypergammaglobulinemia C0001973 Alcoholic intoxication, chronic HSDN C1527344 Dysphonia C0013449 Ear neoplasms HSDN C0018772 Deafness C0011854 Diabetes mellitus, insulin-dependent HSDN C2984058 Have pain C0011981 Diaphragmatic eventration HSDN C4085661 Usual severity nausea C0018916 Hemangioma HSDN C0028738 Nystagmus C2931795 Chromosome 11, deletion 11p OrphaNet C0004134 Dyssynergia C3541306 Plasmodium measurement HSDN C4085210 Usual severity pain C0036472 Scrub typhus HSDN C1519353 Skin eruption papular C0406556 Hereditary acrokeratotic poikiloderma of weary OrphaNet|HPO|MalaCards C0085688 Engorgement breast C1449721 Neonatal breast engorgement UMLS C1963065 Apnea adverse event C1955864 Cardiac sinus arrest HSDN C0349588 Stature short C4015409 Ovarian dysgenesis 4 MalaCards C0917816 Deficiency mental C0796202 Wittwer syndrome MalaCards C0030552 Paralysis partial C3280556 Peripheral neuropathy, myopathy, hoarseness, and hearing loss MalaCards C1963093 Dizziness adverse event C0017636 Glioblastoma HSDN C0020673 Hypothermia (central) (local) C0030297 Pancreatic neoplasm HSDN C0349588 Stature short C1846044 Adrenomyodystrophy OrphaNet|MalaCards C1546759 Specimen source codes - pustule C0406464 Erosive pustular dermatosis of the scalp OrphaNet|MalaCards C0003962 Ascites C0854176 Malignant hepato-biliary neoplasm MalaCards C2032395 Pelvic pain on the left C1547940 Specimen source codes - ulcer HSDN C1963093 Dizziness adverse event C0023530 Leukopenia HSDN C0030794 Pelvis pain C0034065 Pulmonary embolism HSDN C4084784 Diarrhea C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0007758 Cerebellar ataxia C0005695 Bladder neoplasm HSDN C0002962 Angina C0020502 Hyperparathyroidism HSDN C0023380 Lethargy C0022716 Menkes kinky hair syndrome HSDN C0242936 Center pain C0042974 Von willebrand disease HSDN C0020538 Hbp C1857554 Hsd11b2, arg213cys HPO C0013395 Indigestion C0000768 Congenital abnormality HSDN C0005745 Blepharoptosis C0796184 Corpus callosum, agenesis of, with facial anomalies and robin sequence MalaCards C0041667 Low weight C2751321 Macrocephaly, alopecia, cutis laxa, and scoliosis HPO C0000737 Abdomen pain C0376670 Pancreatitis, alcoholic UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0005818 Blood platelet disorders HSDN C1963281 Vomiting adverse event C0270611 Brain damage HSDN C2315100 Pediatric failure to thrive C0018523 Hallervorden-spatz syndrome MalaCards C0018991 Paralysis one side of body C0014118 Endocarditis HSDN C0557874 Global developmental delay C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0022758 Kap HSDN C0018772 Deafness C0546952 Congenital facial asymmetry HSDN C0242936 Center pain C0206681 Adenocarcinoma, clear cell HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020097 Htlv-i infections HSDN C1557397 Adverse event associated with pain C0015423 Eyelid diseases HSDN C1384666 Decreased hearing C0220726 Diastrophic dysplasia MalaCards|HPO C4084768 Usual severity vomiting C0024117 Chronic obstructive airway disease HSDN C2919142 Short stature adverse event C2931093 Osteogenesis imperfecta, type 5 MalaCards C0040264 Ear ringing sound C0034067 Pulmonary emphysema HSDN C0476273 Distress respiratory C1334597 Malignant germ cell neoplasm of mediastinum UMLS C0020538 Hbp C1858054 Bardet-biedl syndrome 6 HPO C0027497 Queasy C0013386 Dyskinesia, drug-induced HSDN C0022346 Yellow skin C1332250 Ampulla of vater small cell carcinoma UMLS C0023015 Language handicap C0008924 Cleft lip HSDN C1963087 Constipation adverse event C1412397 Ancr gene HPO C0221752 Rbc urine C1852456 Cryoglobulinemia, familial mixed OrphaNet|MalaCards C3641756 Have diarrhea C0037650 Somatoform disorder HSDN C3829611 Nausea frequency C0349464 Wernicke-korsakoff syndrome HSDN C0522224 Palsied C1739094 Foodborne botulism OrphaNet|MalaCards C4084784 Diarrhea C0016045 Fibroma HSDN C0018772 Deafness C0039685 Tetralogy of fallot HSDN C1971624 Appetite absent C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0012833 Dizzy C0559260 Congenital scoliosis HSDN C0039070 Collapse fleeting C2676723 Jervell and lange-nielsen syndrome 2 (disorder) MalaCards|HPO C3463815 Feel fatigue C1858361 Pyogenic arthritis, pyoderma gangrenosum and acne OrphaNet|HPO|MalaCards C2984058 Have pain C0002902 Anencephaly HSDN C3641756 Have diarrhea C1623041 Breast-fed HSDN C4085317 Diarrhea frequency C0021843 Intestinal obstruction HSDN C1963137 Hydrocephalus adverse event C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia OrphaNet|HPO|MalaCards C0036572 Convulsion C0040038 Thromboembolism HSDN C3539020 Pelvic pain decreasing in frequency C0033046 Premenstrual syndrome HSDN C0349506 Sun sensitivity C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0009806 Constipate C1839884 Leiomyomatosis, esophageal and vulval, with nephropathy UMLS C0042798 Vision dim C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO C0007758 Cerebellar ataxia C2750234 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 MalaCards|UMLS C0497406 Over weight C1999266 Depression adverse event HSDN C0013395 Indigestion C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C4084768 Usual severity vomiting C0042138 Uterine neoplasms HSDN C0002965 Crescendo angina C0033968 Psychotherapeutic technique HSDN C3274924 Have been coughing C0152938 Secondary pneumonic plague DiseaseOntology|MalaCards C0030193 Sense of pain C0027627 Neoplasm metastasis HSDN C0848203 Male pelvic pain C0002871 Anemia HSDN C0038506 Stutter C0030976 Perceptual distortions HSDN C0518090 Frequency of pain question C0041234 Chagas disease HSDN C0020578 Hyperventilate C0162635 Angelman syndrome HSDN C4084768 Usual severity vomiting C0036202 Sarcoidosis HSDN C4084766 Vomiting C0043515 Zollinger-ellison syndrome HSDN C2237041 Shox gene with short stature C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C2350019 Solitary pulmonary nodule HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0232488 Abdominal colic HSDN C0018681 Headache, cephalalgia C0013990 Pathological accumulation of air in tissues HSDN C0007166 Cardiac output decreased C0041296 Tuberculosis HSDN C2203646 Jaundice C0027643 Neoplasm recurrence, local HSDN C0019079 Bloody sputum C0042974 Von willebrand disease HSDN C3898969 Have been vomiting C0017668 Focal glomerulosclerosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0243001 Abdominal abscess HSDN C0013595 Eczematous dermatitis C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C0020615 Hypoglycemia nos C0751285 Maple syrup urine disease, thiamine responsive HPO C0018784 Deafness sensorineural C0376527 Neoplasm, skull base HSDN C0231528 Muscle pain generalized C3495427 Fanconi-bickel syndrome MalaCards C0027498 Nausea vomiting C0752235 Lyme neuroborreliosis MalaCards C0231218 Malaise generalized C0029835 Other specified tularemia nos DiseaseOntology|MalaCards C0026838 Spasticity muscle C0008677 Bronchitis, chronic HSDN C4084768 Usual severity vomiting C0023470 Myeloid leukemia HSDN C4084773 Bothered by weight gain C0001511 Tissue adhesions HSDN C4084776 Weight loss C0004114 Astrocytoma HSDN C4084726 Distress cough C0034362 Q fever DiseaseOntology|MalaCards C0018784 Deafness sensorineural C1859049 Cchs with hirschsprung disease MalaCards|HPO C0042963 Symptoms vomiting C0238386 Cronkhite-canada disease MalaCards C0018965 Blood urine C0268643 Cystinuria type 1 MalaCards C0009806 Constipate C4062691 Hirschprung's disease UMLS C0751295 Memory loss or impairment C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C0043094 Weight gain C0948441 Venoocclusive disease MalaCards C0012833 Dizzy C0037929 Spinal cord injuries HSDN C4084773 Bothered by weight gain C0013010 Cerebral lateralization HSDN C4085317 Diarrhea frequency C3812171 Bradycardia by ecg finding HSDN C4084725 Usual severity cough C0007099 Carcinoma in situ HSDN C0375557 Abdominal or pelvic swelling, mass, or lump, right upper quadrant C0810319 Other and unspecified gastrointestinal disorders UMLS C0242843 Sweating sickness C0040588 Tracheoesophageal fistula HSDN C0413252 Hypothermia due to exposure C0018621 Hay fever HSDN C3539020 Pelvic pain decreasing in frequency C0041311 Tuberculosis, female genital HSDN C0270948 Neurogenic muscular atrophy C1864851 Pigmented nodular adrenocortical disease, primary, 2 MalaCards C3463815 Feel fatigue C0034951 Refractive errors HSDN C3641756 Have diarrhea C0151699 Intracranial hemorrhages HSDN C4084724 Usual severity constipation C0009376 Colonic polyps HSDN C0002962 Angina C0033847 Pseudoxanthoma elasticum MalaCards|HSDN|HPO C0033774 Skin pruritus C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C0042025 Urinary incontinence stress C4049994 Insulin resistance measurement HSDN C0019825 Voice hoarseness C1833699 Osteopoikilosis, isolated MalaCards|HPO C4085211 Pain distress question C0029877 Ear inflammation HSDN C1557397 Adverse event associated with pain C0026703 Mucopolysaccharidoses HSDN C1963086 Confusion adverse event C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C3887638 Failure to thrive in infant C0265224 Freeman-sheldon syndrome OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0001173 Adult pyloric stenosis HSDN C4084767 Bothered by vomiting C0038362 Stomatitis HSDN C0237326 Defecation pain C1848519 Waardenburg syndrome, type 4a OrphaNet|HPO|MalaCards C0030552 Paralysis partial C2350236 Idiopathic interstitial pneumonias HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0206715 Neoplasms, neuroepithelial HSDN C0151786 Weakness muscle C0004153 Atherosclerosis HSDN C0241137 Skin pallor C1838103 Mitochondrial myopathy and sideroblastic anemia HPO C4084784 Diarrhea C0001314 Acute disease HSDN C2984057 Have nausea C0023676 Life style HSDN C1961131 Cough adverse event C0546837 Malignant neoplasm of esophagus OrphaNet|MalaCards C0015469 Facial paralysis C0796200 Wieacker-wolff syndrome MalaCards C0030200 Intractable pain C0796561 Melanoma vaccines HSDN C1963252 Tremor adverse event C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C1304408 Urticarial vasculitis C4087386 Hypocomplementaemic urticarial vasculitis syndrome UMLS C3641755 Have constipation C0039128 Syphilis HSDN C2315100 Pediatric failure to thrive C0265246 Townes syndrome MalaCards|HPO C4085661 Usual severity nausea C0021295 Infant, premature, diseases HSDN C0015672 Decreased energy C0001486 Adenovirus infections HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0007766 Intracranial aneurysm HSDN C0031911 Pigment deposition C1704376 Uterine corpus carcinosarcoma MalaCards C0026838 Spasticity muscle C0023944 Cerebromedullospinal disconnection OrphaNet|MalaCards C0030552 Paralysis partial C0036341 Schizophrenia HSDN C0036572 Convulsion C0268228 Neuraminidase 1 deficiency OrphaNet|HPO C0018989 Paresis of one side of body C0268407 Senile cardiac amyloidosis MalaCards C0242936 Center pain C0040409 Tongue diseases HSDN C0003107 Anogenital pruritus C0810052 Other inflammatory condition of skin UMLS C0557874 Global developmental delay C4015186 Monocarboxylate transporter 1 deficiency MalaCards C0009806 Constipate C3897531 Stage iiia rectal cancer UMLS C0917816 Deficiency mental C0268119 Combined molybdoflavoprotein enzyme deficiency HPO C0013604 Edematous C1266119 Solitary fibrous tumor HSDN C0577564 Mass of lymphoreticular structure C0282609 Bone marrow neoplasms UMLS C0022346 Yellow skin C0947622 Cholecystolithiasis HSDN C3887873 Hearing loss C0262584 Carcinoma, small cell HSDN C3827868 Tachycardia by ecg finding C0752355 Myotonia fluctuans (disorder) MalaCards C0520966 Coordination impaired C0003635 Apraxias UMLS C0018524 Hallucinate C1962976 Ventricular fibrillation adverse event HSDN C0424755 Fever symptoms C0001255 Actinomycetales infections HSDN C0454644 Delayed language development C1858054 Bardet-biedl syndrome 6 HPO C0151908 Dry skin C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO|UMLS C0242936 Center pain C0035317 Retinal hemorrhage HSDN C0010200 Cough symptom C0011175 Dehydration UMLS C0150045 Urinary incontinence urge C0262655 Recurrent urinary tract infection HSDN C4084723 Constipation C0268242 Niemann-pick disease, type a MalaCards|HPO C4084802 Usual severity diarrhea C0026918 Mycobacterium infections HSDN C0151908 Dry skin C0796126 Aicardi-goutieres syndrome 1 MalaCards C0026821 Cramp C1962986 Glaucoma adverse event HSDN C0042798 Vision dim C0393551 Madras-type motor neurone disease MalaCards C2024893 Cardiovascular surgery result: fatigue C2930674 Babesioses, human MalaCards C0028738 Nystagmus C1850599 Leigh syndrome due to mitochondrial complex iv deficiency HPO C0039070 Collapse fleeting C2984299 Asthma pathway HSDN C1260880 Nasal drip C1336408 Paranasal sinus cancer stage ivc UMLS C0242936 Center pain C0677866 Brain stem neoplasms HSDN C0008031 Pain chest C0040582 Trachea neoplasm HSDN C2024878 Cardiovascular surgery result: dyspnea C1962979 Burn adverse event HSDN C0518090 Frequency of pain question C0040028 Thrombocythemia, essential HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0036864 Sexual relations HSDN C0019079 Bloody sputum C0023269 Leiomyosarcoma HSDN C0413252 Hypothermia due to exposure C0021655 Insulin resistance HSDN C0020673 Hypothermia (central) (local) C0038661 Suicide HSDN C0015469 Facial paralysis C0037974 Spirochaetales infections HSDN C0013428 Painful urination C0497572 Female genital herpes HSDN C0015799 Feminisation C0001622 Adrenal gland hyperfunction HSDN C4084769 Vomiting frequency C0080179 Vertebra fracture HSDN C0018772 Deafness C1423541 Vangl2 gene HSDN C0030554 Abnormal sensation C1578691 Congenital myxedema MalaCards C0018681 Headache, cephalalgia C0343376 B; paratyphoid fever DiseaseOntology|MalaCards C2984058 Have pain C0025149 Medulloblastoma HSDN C4084773 Bothered by weight gain C0021845 Intestinal perforation HSDN C4084773 Bothered by weight gain C0013575 Ectodermal dysplasia HSDN C0009806 Constipate C0030297 Pancreatic neoplasm HSDN C2242996 Tingling C0037937 Spine injury HSDN C0000737 Abdomen pain C2242987 Benign mastocytoma MalaCards C0033377 Caudal displacement C1834523 Arthrogryposis, distal, type 2b OrphaNet|HPO|MalaCards C0040485 Wryneck C0037928 Spinal cord diseases HSDN C0037384 Snore C4014419 Xia-gibbs syndrome MalaCards|UMLS C0032617 High urine output C0042075 Urologic diseases HSDN|UMLS C4085862 Bothered by nausea C2936636 Anticipation, psychological HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018418 Gynecomastia HSDN C0007758 Cerebellar ataxia C0023530 Leukopenia HSDN C0036572 Convulsion C0751188 Dural headache post puncture HSDN C3898969 Have been vomiting C0030319 Panic disorder HSDN C4084727 Cough frequency C2911643 Encounter due to family history of osteoporosis HSDN C0013404 Respiratory difficulty C0524688 Pneumonic plague DiseaseOntology|MalaCards C0009763 Conjunctiva inflammation C1848410 Xeroderma pigmentosum, variant type MalaCards|HPO C4084725 Usual severity cough C1266101 Thymic epithelial tumor OrphaNet C0037763 Spasm C0035126 Reperfusion injury HSDN C0162298 Stiffness joints C0013366 Dyschondroplasia OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0027625 Circulating neoplastic cells HSDN C0000727 Abdomen acute C0006434 Burn injury HSDN C0497406 Over weight C0003615 Appendicitis HSDN C0018772 Deafness C0014065 Congenital cerebral hernia HSDN C0020672 Body temperature decreased C0041956 Ureteral obstruction HSDN C4084802 Usual severity diarrhea C0038013 Ankylosing spondylitis HSDN C0013604 Edematous C0035920 Rubella HSDN C0036572 Convulsion C0014457 Eosinophilia HSDN C0011991 Loose stools C0007873 Uterine cervical neoplasm HSDN C0009792 Consciousness disorder C0031941 Pineal gland neoplasm HSDN C0000737 Abdomen pain C0029106 Opisthorchiasis DiseaseOntology C3641756 Have diarrhea C0014852 Esophageal diseases HSDN C3539892 Pelvic pain in front C0003873 Rheumatoid arthritis HSDN C1549543 Administration method - pain C0376545 Hematologic neoplasms HSDN C3641756 Have diarrhea C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C0518090 Frequency of pain question C0018920 Hemangioma, cavernous HSDN C4084724 Usual severity constipation C0032343 Poisoning HSDN C0015672 Decreased energy C0019061 Hemolytic-uremic syndrome HSDN C2919142 Short stature adverse event C1527168 Bonnevie-ullrich syndrome MalaCards C4084723 Constipation C3149848 Variegate porphyria, homozygous variant HPO C0013604 Edematous C0018674 Head trauma HSDN C0857305 Thrombocytopenia purpura C0024121 Lung neoplasms HSDN C3898969 Have been vomiting C0243025 Hantavirus pulmonary syndrome MalaCards C1557397 Adverse event associated with pain C0018133 Graft-vs-host disease HSDN C0027497 Queasy C1299624 Postural orthostatic tachycardia syndrome HSDN C0040264 Ear ringing sound C0751771 Sleep bruxism HSDN C0023012 Delay language C3280799 Cutis laxa, autosomal recessive, type iiib MalaCards C0011991 Loose stools C0011175 Dehydration UMLS C0018772 Deafness C1852542 Cdo syndrome MalaCards C4085548 Usual severity dizziness C0032816 Post-concussion headache HSDN C1971624 Appetite absent C0041351 Tularemia HSDN C0018681 Headache, cephalalgia C0029456 Osteoporosis HSDN C0011991 Loose stools C0162871 Aortic aneurysm, abdominal HSDN C0162298 Stiffness joints C1860464 Congenital ptosis and posterior fusion of lumbosacral vertebrae OrphaNet|MalaCards C1549543 Administration method - pain C0030353 Papilledema HSDN C4042891 Sleep wake disorders C0013295 Duodenal ulcer HSDN C3539890 Pelvic pain causes awakening at night C0007867 Cervix diseases HSDN C0349489 Fetal hypoxia C0233315 Premature birth of newborn HSDN C0026838 Spasticity muscle C0002871 Anemia HSDN C0522224 Palsied C0027932 Neurotic disorders HSDN C0003550 Broca aphasia C0007781 Intracranial embolism and thrombosis HSDN C0042928 Paralysis vocal cord C0029408 Degenerative polyarthritis HSDN C4084725 Usual severity cough C0037579 Soft tissue neoplasms HSDN C2237041 Shox gene with short stature C3554002 Pbd12a MalaCards C0018775 Hearing loss bilateral C0024054 Lown-ganong-levine syndrome HSDN C0030552 Paralysis partial C0035354 Axon reaction HSDN C0011991 Loose stools C0016719 Friedreich ataxia HSDN C0007758 Cerebellar ataxia C0752155 Central nervous system vascular malformations HSDN C4084774 Have weight loss C0020517 Hypersensitivity HSDN C0013404 Respiratory difficulty C0028796 Dermatitis, occupational HSDN C0242936 Center pain C0041309 Tuberculosis, cutaneous HSDN C0030193 Sense of pain C0543820 Erythromelalgia, secondary UMLS C0010200 Cough symptom C0027055 Myocardial reperfusion injury HSDN C0030552 Paralysis partial C0027059 Myocarditis HSDN C1836296 Lower extremity weakness C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C1963252 Tremor adverse event C0033578 Prostatic neoplasms HSDN C0027796 Neuralgias C0003803 Arnold chiari malformation HSDN C0155552 Hearing loss mixed C1546558 Specimen source codes - blister HSDN C1963252 Tremor adverse event C0037369 Smoking HSDN C0000737 Abdomen pain C1332166 Adenocarcinoma of the gastroesophageal junction UMLS C0023012 Delay language C1857802 Morm syndrome HPO C0035229 Respiratory function impaired C0175691 Dubowitz syndrome OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0009952 Febrile convulsions HSDN C0232461 Increased appetite C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0027497 Queasy C0033817 Pseudomonas infections HSDN C0221752 Rbc urine C0268164 Primary hyperoxaluria, type i OrphaNet|HPO C0002962 Angina C0007787 Transient ischemic attack HSDN C4084773 Bothered by weight gain C0032897 Prader-willi syndrome HSDN C2984058 Have pain C0043528 Zoonoses HSDN C4084775 Usual severity weight loss C1552262 Nurse practitioner - family HSDN C0030200 Intractable pain C0033578 Prostatic neoplasms HSDN C3463815 Feel fatigue C0008479 Chondrosarcoma HSDN C0042024 Urine incontinence C0085183 Neoplasms, second primary HSDN C4084766 Vomiting C1963211 Pericarditis adverse event HSDN C0035078 Failure kidney C1841679 Hand foot uterus syndrome HPO C4085661 Usual severity nausea C0033975 Psychotic disorders HSDN C2237041 Shox gene with short stature C2931292 Curatolo cilio pessagno syndrome OrphaNet|MalaCards C0040034 Thrombocytopenia C0019099 Hemorrhagic fever, crimean MalaCards C0020578 Hyperventilate C0034065 Pulmonary embolism HSDN C0027796 Neuralgias C0032019 Pituitary neoplasms HSDN C1069915 Vertigo C0033860 Psoriasis HSDN C0036396 Sciatica C0038013 Ankylosing spondylitis HSDN C0039070 Collapse fleeting C0851578 Sleep disorders UMLS C0034155 Thrombotic thrombocytopenic purpura C0024305 Lymphoma, non-hodgkin HSDN C0006370 Bulimia C4042893 Person centered therapy HSDN C0424755 Fever symptoms C0017589 Farcy DiseaseOntology|MalaCards C1961131 Cough adverse event C0009917 Contracture HSDN C1384666 Decreased hearing C0042029 Urinary tract infection HSDN C4050613 Anxiety C3711850 Opticospinal multiple sclerosis MalaCards C0013404 Respiratory difficulty C0023976 Long qt syndrome HSDN C0424755 Fever symptoms C0021334 Infectious bovine rhinotracheitis HSDN C0037199 Sinus infection C0342200 Endemic cretinism MalaCards C0026826 High muscle tone C0243010 Viral encephalitis HSDN C0231528 Muscle pain generalized C2930674 Babesioses, human MalaCards C1565249 Limitation, mobility C0005944 Metabolic bone disorder HSDN C1527344 Dysphonia C3542413 Cdisc adas-cog - comprehension HSDN C0030554 Abnormal sensation C0007787 Transient ischemic attack HSDN C0013604 Edematous C0043241 Wound infection HSDN C0016199 Pain flank C0013922 Embolism HSDN C3274924 Have been coughing C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0036572 Convulsion C1859878 Alopecia-mental retardation syndrome 1 MalaCards C3887638 Failure to thrive in infant C1855772 Absent corpus callosum cataract immunodeficiency MalaCards|HPO C1963093 Dizziness adverse event C0006434 Burn injury HSDN C0557874 Global developmental delay C2937419 Chromosome x pentasomy OrphaNet|MalaCards C1962956 Flatulence adverse event C0198632 Pneumoperitoneum HSDN C0041657 Consciousness loss C0014547 Epilepsies, partial HSDN C0237326 Defecation pain C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C4084727 Cough frequency C0524851 Neurodegenerative disorders HSDN C0231528 Muscle pain generalized C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0020639 Hypoproteinaemia C0017155 Gastritis, hypertrophic MalaCards C0034933 Abnormal reflexes C0021843 Intestinal obstruction HSDN C2096293 Ent surgical result ear vertigo C0398691 Hyperimmunoglobulinemia d MalaCards|HPO C0231528 Muscle pain generalized C0008049 Chicken pox DiseaseOntology|MalaCards C0030193 Sense of pain C0267397 Alimentary pain due to vascular insufficiency UMLS C0034150 Skin purpura C0030305 Pancreatitis HSDN C0033774 Skin pruritus C0243026 Sepsis HSDN C0013405 Dyspnea, paroxysmal C0010068 Coronary heart disease HSDN C1959630 Eye pain adverse event C0751878 Vasculitis, central nervous system HSDN C0000737 Abdomen pain C0158683 Polycystic liver disease MalaCards|HPO C0003811 Cardiac rhythm disturbance C0034155 Purpura, thrombotic thrombocytopenic MalaCards|HSDN C0917816 Deficiency mental C4014419 Xia-gibbs syndrome MalaCards C0086565 Liver function abnormal C0334299 Carcinoid tumor no icd-o subtype MalaCards C0026884 Muteness C0796070 Microphthalmia, syndromic 7 MalaCards C1549543 Administration method - pain C2116082 Finding of thyroid nodule by palpation HSDN C0917816 Deficiency mental C1855304 Mental retardation, autosomal recessive 1 HPO C4084802 Usual severity diarrhea C0043397 Yellow fever, jungle MalaCards C0424755 Fever symptoms C0276932 Schistosoma; intercalatum DiseaseOntology C1882272 Pain adverse event by ctcae anatomic descriptor C0015959 Fetomaternal bleeding HSDN C4084725 Usual severity cough C0030920 Peptic ulcer HSDN C0015469 Facial paralysis C0042109 Urticaria HSDN C4084725 Usual severity cough C0026764 Multiple myeloma HSDN C0007758 Cerebellar ataxia C0206247 Amyloid neuropathies MalaCards C2984058 Have pain C0011311 Dengue fever HSDN C0085642 Asphyxia reticularis C2267227 Bulimia nervosa HSDN C4042891 Sleep wake disorders C0019372 Herpesviridae infections HSDN C0024031 Back pain lower back C0033860 Psoriasis HSDN C0242936 Center pain C0023761 Lip neoplasms HSDN C0558920 Thigh mass C3164848 Melanocytic naevus of skin of thigh UMLS C3815497 Cough C0032290 Aspiration pneumonia MalaCards C3539890 Pelvic pain causes awakening at night C0010356 Cross infection HSDN C2919142 Short stature adverse event C0029421 Osteochondritis dissecans HPO C1069915 Vertigo C0034183 Pyelitis unspecified HSDN C4084784 Diarrhea C0035613 Rift valley fever OrphaNet|MalaCards C1384666 Decreased hearing C0021051 Immunologic deficiency syndromes HSDN C0085636 Light sensitivity C0004576 Babesiosis MalaCards C4085210 Usual severity pain C0158454 Malunited fracture HSDN C1963252 Tremor adverse event C0221061 Behr syndrome MalaCards C3539891 Pelvic pain to the rear C0037051 Behavior illness HSDN C0037763 Spasm C3539923 Cdisc adas-cog - orientation summary score HSDN C4084727 Cough frequency C0034072 Cor pulmonale HSDN C0018772 Deafness C0035126 Reperfusion injury HSDN C0016512 Pain foot C4038661 Pops - painful os peroneum syndrome UMLS C0349588 Stature short C1849453 Rapadilino syndrome MalaCards|HPO C0026205 Pupillary constriction C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0018681 Headache, cephalalgia C0017412 Genital diseases, male HSDN C4084784 Diarrhea C0020413 Hymenolepiasis DiseaseOntology|HSDN C2315100 Pediatric failure to thrive C0406587 Wrinkly skin syndrome MalaCards|HPO C0030794 Pelvis pain C0019066 Nontraumatic hemoperitoneum HSDN C4084727 Cough frequency C0030286 Pancreatic diseases HSDN C0015672 Decreased energy C0855099 Small lymphocytic lymphoma, stage ii UMLS C0037316 Not enough sleeping C0051981 Anti-leprosy vaccine HSDN C0427055 Face weakness C0025235 Melkersson-rosenthal syndrome OrphaNet|MalaCards C2919142 Short stature adverse event C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0018772 Deafness C0003492 Aortic coarctation HSDN C2919142 Short stature adverse event C4053775 Pituitary stalk interruption syndrome MalaCards C0264611 Apraxia of speech C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C4084727 Cough frequency C0023676 Life style HSDN C0241210 Speaking delay C3665349 Secondary hypothyroidism OrphaNet|MalaCards C4084802 Usual severity diarrhea C0032285 Pneumonia HSDN C0851578 Disorder sleep C0997768 Glaucoma HSDN C1557397 Adverse event associated with pain C0398738 Leukocyte adhesion deficiency type 1 MalaCards C2029884 Hearing loss by exam C2911643 Encounter due to family history of osteoporosis HSDN C2911647 Weight gain adverse event C1285261 Fetal nutrition disorders HSDN C2911647 Weight gain adverse event C0079744 Diffuse large b-cell lymphoma HSDN C4084723 Constipation C0037579 Soft tissue neoplasms HSDN C4084774 Have weight loss C0162526 Aids-related opportunistic infections HSDN C0009421 Comatose C1623041 Breast-fed HSDN C3665347 Vision impaired C0339085 Blepharochalasis, struma, double lip syndrome OrphaNet|MalaCards C0042571 Vertigo subjective C0003469 Anxiety disorders HSDN C0040034 Thrombocytopenia C0340978 May-hegglin anomaly HPO C0030200 Intractable pain C0026552 Morphine dependence HSDN C0728710 Pupil constriction observed C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0036572 Convulsion C4273988 Benign adult familial myoclonic epilepsy UMLS C1384666 Decreased hearing C0001430 Adenoma HSDN C0349588 Stature short C2678051 Mental retardation, x-linked 94 (disorder) MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0038436 Post-traumatic stress disorder HSDN C1971624 Appetite absent C0220847 C hepatitis virus HSDN C0003862 Pain joint C0003469 Anxiety disorders HSDN C0026821 Cramp C0010346 Crohn disease HSDN C4085211 Pain distress question C0023484 Leukemia, plasma cell HSDN C0151786 Weakness muscle C1856305 Gsd iv, neuromuscular form, childhood MalaCards|HPO C3463815 Feel fatigue C0001231 Acth syndrome, ectopic MalaCards C1963091 Diarrhea adverse event C0079744 Diffuse large b-cell lymphoma HSDN C0008031 Pain chest C0016053 Fibromyalgia HSDN C1145670 Failure respiratory C0265282 Fibrochondrogenesis OrphaNet|HPO|MalaCards C4084784 Diarrhea C1423541 Vangl2 gene HSDN C0011991 Loose stools C2749484 Neuroblastoma, susceptibility to HPO C0019209 Large liver C0085110 Severe combined immunodeficiency MalaCards C0040822 D tremors C1859298 Spinocerebellar ataxia, autosomal recessive 2 MalaCards|UMLS C1962972 Proteinuria adverse event C0015397 Disorder of eye HSDN C3898969 Have been vomiting C2717906 Hereditary angioedema type i HPO C0557874 Global developmental delay C0268579 Propionic acidemia OrphaNet|HPO C0012569 Double vision C0236969 Substance-related disorders HSDN C0026858 Musculoskeletal pain C2936631 Complaint, subjective health HSDN C2911647 Weight gain adverse event C2073625 X-ray of chest: pleural effusion HSDN C0030552 Paralysis partial C2752015 Glycogen storage disease xiv MalaCards C0013404 Respiratory difficulty C1336224 Stage iiib large cell carcinoma of lung UMLS C0009676 Confusion state C0751587 Cadasil syndrome OrphaNet|HPO C4085317 Diarrhea frequency C0002895 Anemia, sickle cell HSDN C4084788 Have dizziness C1962986 Glaucoma adverse event HSDN C0024031 Back pain lower back C0018213 Graves disease HSDN C0042024 Urine incontinence C0004352 Autistic disorder HSDN C1963093 Dizziness adverse event C0001973 Alcoholic intoxication, chronic HSDN C4084775 Usual severity weight loss C0007781 Intracranial embolism and thrombosis HSDN C4084725 Usual severity cough C0004114 Astrocytoma HSDN C0018772 Deafness C0574085 3-methylglutaconic aciduria type 4 MalaCards C1962972 Proteinuria adverse event C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C3539890 Pelvic pain causes awakening at night C0206654 Leiomyomatosis HSDN C3539023 Pelvic pain increasing in frequency C2936290 Femoracetabular impingement HSDN C3658248 Enlarged waist elevated triglycerides C0007273 Carotid artery diseases HSDN C0022346 Yellow skin C0042029 Urinary tract infection HSDN C0018784 Deafness sensorineural C0032371 Poliomyelitis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0520909 Ponv C0033578 Prostatic neoplasms HSDN C0030554 Abnormal sensation C0080274 Urinary retention HSDN C0860603 Anxiety symptom C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C2024878 Cardiovascular surgery result: dyspnea C0001418 Adenocarcinoma HSDN C0042420 Vasovagal episode C0003813 Arrhythmia sinus HSDN C4084774 Have weight loss C0029463 Osteosarcoma HSDN|HPO C4084726 Distress cough C0149514 Bronchitis acute MalaCards C4084784 Diarrhea C0002940 Aneurysm HSDN C4084766 Vomiting C0206644 Histiocytoma, benign fibrous HSDN C0013132 Drooling C0086650 Mps iii d HPO C0011991 Loose stools C0085258 Deficiency, yang HSDN C0010200 Cough symptom C0026650 Movement disorders HSDN C0018777 Deafness, conductive C1860787 Down syndrome critical region HPO C4084723 Constipation C0023467 Leukemia, myelocytic, acute HSDN C1384666 Decreased hearing C0019104 Hemorrhagic fevers, viral MalaCards C0036396 Sciatica C0019693 Hiv infections HSDN C4085210 Usual severity pain C0037275 Skin diseases, vesiculobullous HSDN C0039070 Collapse fleeting C1263846 Attention deficit hyperactivity disorder HSDN C0221166 Paraparesis C3888102 Frontotemporal dementia with motor neuron disease MalaCards C0036572 Convulsion C4225421 Linear skin defects with cardiomyopathy and other congenital anomalies UMLS C4084784 Diarrhea C0043528 Zoonoses HSDN C0149745 Ulcer mouth C2931868 Catalase deficiency MalaCards C4084766 Vomiting C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0026821 Cramp C3494506 Pseudohypoparathyroidism, type ia HPO C3539020 Pelvic pain decreasing in frequency C0242350 Erectile dysfunction HSDN C0000737 Abdomen pain C0206634 Liposarcoma, myxoid MalaCards|HPO C1263846 Attention deficit disorder with hyperactivity C3697269 15q24 microdeletion HPO C3539022 Pelvic pain decreasing in severity C0206630 Endometrial stromal sarcoma HSDN C0023012 Delay language C1876161 Ceroid lipofuscinosis, neuronal, 2 MalaCards|HPO C3815497 Cough C0034531 Experimental radiation injuries HSDN C0019214 Hepatosplenomegaly C1416865 Lipa gene HPO C1963252 Tremor adverse event C1556682 Adverse event associated with infection HSDN C0042024 Urine incontinence C0008065 Childhood behavior HSDN C1999266 Depression adverse event C1527406 Rhizomelic pseudopolyarthritis MalaCards C4085661 Usual severity nausea C0025281 Meniere disease HSDN C4084726 Distress cough C0021845 Intestinal perforation HSDN C0018524 Hallucinate C0162671 Melas syndrome OrphaNet|HSDN|HPO|MalaCards C2032396 Pelvic pain on the right C0001261 Actinomycosis HSDN C0037317 Sleep disturbance C1868570 Char syndrome MalaCards|HPO C0011991 Loose stools C0038579 Substance abuse, intravenous HSDN C1963184 Nystagmus adverse event C2751308 Cone dystrophy 4 (disorder) MalaCards|HPO C2984057 Have nausea C0042076 Urologic neoplasms HSDN C0019214 Hepatosplenomegaly C0795878 Monosomy 22 MalaCards C0020505 Excessive eating C0700201 Dyssomnias HSDN C0042024 Urine incontinence C0019151 Hepatic encephalopathy HSDN C0424755 Fever symptoms C0037304 Skull fracture HSDN C0026821 Cramp C0020625 Hyponatremia HSDN C0497247 Blood pressure elevation C1619700 Renal adysplasia MalaCards|HPO C0231218 Malaise generalized C0862967 Recurrent cholangiocarcinoma UMLS C0013421 Dystonia C0003811 Cardiac arrhythmia HSDN C0015469 Facial paralysis C0030305 Pancreatitis HSDN C0041657 Consciousness loss C0018802 Congestive heart failure HSDN C3641756 Have diarrhea C1535939 Pneumocystis jiroveci pneumonia HSDN C0522224 Palsied C0021933 Intussusception HSDN C0406408 Reflex urticaria C0021368 Inflammation UMLS C0002624 Amnesia retrograde C0027531 Neck injury HSDN C0018780 Frequencies hearing high loss C1963138 Hypertension adverse event HSDN C0042024 Urine incontinence C1527231 Adrenomyeloneuropathy MalaCards|HPO C0038002 Spleen enlargement C0034960 Refsum disease OrphaNet|HPO C4084775 Usual severity weight loss C0030805 Bullous pemphigoid OrphaNet|HPO|MalaCards C2029884 Hearing loss by exam C0524851 Neurodegenerative disorders HSDN C0036659 Sensation disorder C0752235 Lyme neuroborreliosis HSDN C0018991 Paralysis one side of body C0027531 Neck injury HSDN C0037771 Paraparesis spastic C3553960 Peroxisome biogenesis disorder 8b MalaCards C0013395 Indigestion C0002895 Anemia, sickle cell HSDN C0009421 Comatose C0007097 Carcinomas HSDN C3641755 Have constipation C0042075 Urologic diseases MalaCards C0000737 Abdomen pain C1963216 Proctitis adverse event HSDN C0034063 Edema lung C0852283 Respiratory distress syndrome MalaCards C0424755 Fever symptoms C0014848 Esophageal achalasia HSDN C0002965 Crescendo angina C0036421 Systemic scleroderma HSDN C0031911 Pigment deposition C0154860 Hereditary retinal dystr. nos MalaCards C1963086 Confusion adverse event C0003469 Anxiety disorders HSDN C3829611 Nausea frequency C0020875 Ileal diseases HSDN C3665492 Pigmentations C0751291 Desmoplastic medulloblastoma MalaCards C0000727 Abdomen acute C0010068 Coronary heart disease HSDN C1549543 Administration method - pain C0021831 Intestinal diseases HSDN C0036396 Sciatica C0033968 Psychotherapeutic technique HSDN C0233794 Memory impaired C1843013 Alzheimer disease, familial, type 3 HPO C1549543 Administration method - pain C0026683 Mucocele HSDN C3665347 Vision impaired C0342681 Minimal pigment oculocutaneous albinism MalaCards C1549543 Administration method - pain C0029440 Osteoma HSDN C0424755 Fever symptoms C0022680 Polycystic kidney diseases HSDN C0007758 Cerebellar ataxia C0035435 Rheumatism HSDN C1963091 Diarrhea adverse event C0878544 Cardiomyopathies HSDN C3829611 Nausea frequency C0085278 Antiphospholipid syndrome HSDN C4085317 Diarrhea frequency C0029927 Ovarian cysts HSDN C0033377 Caudal displacement C0796117 Pitt syndrome MalaCards C0278152 Hemifacial spasms C1306710 Facial asymmetry HSDN C2315100 Pediatric failure to thrive C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0154694 Spastic hemiplegia UMLS C0042798 Vision dim C3495589 Jalili syndrome OrphaNet|HPO|MalaCards C0020580 Decreased sensation C0038531 Subclavian artery stenosis HSDN C2096293 Ent surgical result ear vertigo C0020456 Hyperglycemia HSDN C2203646 Jaundice C1552527 Clinic / center - developmental disabilities HSDN C3641755 Have constipation C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C0557874 Global developmental delay C4015444 Mental retardation, autosomal recessive 47 MalaCards C0023012 Delay language C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0008928 Cleidocranial dysplasia HSDN C0035229 Respiratory function impaired C2930851 Intestinal lipophagic granulomatosis MalaCards C0522224 Palsied C0023281 Leishmaniasis HSDN C0700590 Diaphoresis excessive C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0019542 Higher nervous activity HSDN C0004604 Pain back C0030319 Panic disorder HSDN C4084802 Usual severity diarrhea C0006277 Bronchitis HSDN C1961131 Cough adverse event C0020732 Iatrogenic disease HSDN C4085661 Usual severity nausea C0997768 Glaucoma HSDN C0018681 Headache, cephalalgia C0521665 Chronic mixed headache syndrome UMLS C0522224 Palsied C0268446 Thyrotoxic periodic paralysis OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0034362 Q fever HSDN C0002962 Angina C1527311 Brain edema HSDN C3541349 Syncope C0010054 Coronary arteriosclerosis HSDN C0242670 Chronic vegetative state C0038538 Effusion subdural HSDN C0751327 Hypertonia, neonatal C3553288 Hyperekplexia 3 MalaCards C0497406 Over weight C0008350 Cholelithiasis HSDN C1145670 Failure respiratory C0264743 Rheumatic fever without heart involvement MalaCards C3203358 Alveolar hypoventilation C1458155 Mammary neoplasms HSDN C0013604 Edematous C0008476 Chondromatosis, synovial HSDN C3463815 Feel fatigue C0027743 Nerve compression syndrome HSDN C0917816 Deficiency mental C0271568 Laron syndrome HPO C4085210 Usual severity pain C0017920 Glycogen storage disease type i HSDN C4084766 Vomiting C0037926 Compression of spinal cord HSDN C0018772 Deafness C0391826 Lhermitte-duclos disease MalaCards|HPO C0024031 Back pain lower back C1263846 Attention deficit hyperactivity disorder HSDN C4084784 Diarrhea C0021568 Bites insect stings HSDN C0522224 Palsied C0023119 Lathyrism HSDN C0012569 Double vision C0460136 Barotrauma HSDN C0848332 Abnormal skin spots C0406613 Site-specific disorder of skin UMLS C2237041 Shox gene with short stature C3536983 Familial hypophosphatemic rickets OrphaNet|HPO|MalaCards C0000737 Abdomen pain C4086167 Childhood ovarian mixed germ cell tumor UMLS C0042963 Symptoms vomiting C0027947 Neutropenia HSDN C0860603 Anxiety symptom C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C1963184 Nystagmus adverse event C1857780 Joubert syndrome 5 MalaCards|HPO C1963091 Diarrhea adverse event C0035258 Restless legs syndrome HSDN C0035229 Respiratory function impaired C3280054 Geleophysic dysplasia 2 MalaCards C0518090 Frequency of pain question C0039236 Tachycardia episodic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0025290 Aseptic meningitis HSDN C0020538 Hbp C0281479 Primary systemic amyloidosis MalaCards C1963064 Anxiety adverse event C0025268 Multiple endocrine neoplasia type 2a OrphaNet C1962972 Proteinuria adverse event C0033923 Psychomotor function HSDN C0018772 Deafness C0268233 Galactosialidosis OrphaNet|HPO|MalaCards C0002962 Angina C0032326 Pneumothorax HSDN C0024031 Back pain lower back C0024305 Lymphoma, non-hodgkin HSDN C1963063 Anorexia adverse event C0035613 Rift valley fever MalaCards C1963087 Constipation adverse event C0006663 Calcinosis HSDN C0522224 Palsied C0262584 Carcinoma, small cell HSDN C0026603 Motion sickness C0034929 Reflex HSDN C4085549 Dizziness C0021655 Insulin resistance HSDN C0018834 Brash C0020701 Somatization disorder HSDN C0000737 Abdomen pain C0398597 Histiocytic syndrome HSDN C3665347 Vision impaired C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO C1963252 Tremor adverse event C0029882 Otitis media HSDN C0011168 Disorder deglutition C1843366 Niemann-pick disease, type c2 MalaCards|HPO C1384666 Decreased hearing C0036472 Scrub typhus HSDN C4084724 Usual severity constipation C0020649 Hypotension HSDN C3463815 Feel fatigue C0007760 Cerebellar diseases HSDN C4085222 Nausea C1555914 Psychologist - psychotherapy, group HSDN C0038990 Sweats C0343110 Epidermolytic palmoplantar keratoderma of vorner OrphaNet|HPO C0000737 Abdomen pain C0079504 Hermanski-pudlak syndrome MalaCards|HPO C1963137 Hydrocephalus adverse event C0020256 Congenital hydrocephalus OrphaNet C1069915 Vertigo C0700327 Clinical findings relating to memory HSDN C4084774 Have weight loss C0014863 Esophageal spasm diffuse HSDN C0032617 High urine output C0405580 Adrenal cortical hypofunction HSDN C0042755 Virilisation C0042994 Vulvar diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242350 Erectile dysfunction HSDN C0030193 Sense of pain C1862939 Amyotrophic lateral sclerosis 1 MalaCards C2315100 Pediatric failure to thrive C1401162 Carbohydrate intolerance MalaCards C1963180 Neck pain adverse event C0220847 C hepatitis virus HSDN C0349588 Stature short C0406729 Berlin syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0020523 Immediate hypersensitivity HSDN C0019079 Bloody sputum C0742290 Chest pain char pleuritic UMLS C0011168 Disorder deglutition C2931905 Olivopontocerebellar atrophy 3 MalaCards C2919142 Short stature adverse event C1850625 Native american myopathy MalaCards|HPO C0015469 Facial paralysis C3163620 Hypotension adverse event HSDN C1963137 Hydrocephalus adverse event C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C0476280 Chest pain musculoskeletal C0575032 Thoracic facet syndrome UMLS C3641755 Have constipation C0027819 Neuroblastoma HSDN C1000483 Genus anemia C0406557 Poikiloderma of kindler MalaCards|HPO C0015676 Mental fatigue C0026896 Myasthenia gravis HSDN C0150055 Pain chronic C1458155 Mammary neoplasms HSDN C0009421 Comatose C1269683 Major depressive disorder HSDN C0038868 Supranuclear palsy progressive C0020258 Hydrocephalus, normal pressure HSDN C0013404 Respiratory difficulty C0023381 Letterer-siwe disease MalaCards C2096293 Ent surgical result ear vertigo C0023418 Leukemia HSDN C0518090 Frequency of pain question C0025500 Mesothelioma HSDN C0151908 Dry skin C0011644 Scleroderma OrphaNet|MalaCards C0000737 Abdomen pain C0278713 Wilm's tumor, stage iii UMLS C0151786 Weakness muscle C2350236 Idiopathic interstitial pneumonias HSDN C0018965 Blood urine C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C1963184 Nystagmus adverse event C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C0162298 Stiffness joints C2931338 Chromosome 3, monosomy 3q13 OrphaNet|MalaCards C0022346 Yellow skin C0302280 Adrenogenital syndrome HSDN C0021359 Infertility C2931374 Al awadi teebi farag syndrome OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C1168250 Laryngopharyngeal reflux HSDN C4084774 Have weight loss C0019270 Hernia HSDN C4084767 Bothered by vomiting C3888018 Congenital hyperinsulinism MalaCards C2029884 Hearing loss by exam C1881674 Medical device emits smoke HSDN C4084767 Bothered by vomiting C1000483 Genus anemia HSDN C3539890 Pelvic pain causes awakening at night C0042065 Genitourinary neoplasms HSDN C0740961 Amputation stump pain C0740962 Amputation stump swelling UMLS C0030486 Extremity paralysis, lower C0012979 Canine disease HSDN C0917816 Deficiency mental C1832390 Van maldergem wetzburger verloes syndrome MalaCards|HPO C2096293 Ent surgical result ear vertigo C0161409 Cochlear nerve damage HSDN C3463815 Feel fatigue C0151467 Addisonian crisis OrphaNet|MalaCards C0015672 Decreased energy C0030521 Parathyroid neoplasms MalaCards C2911645 Weight loss adverse event C0012817 Diverticulum HSDN C2315100 Pediatric failure to thrive C0079299 Epidermolysis bullosa simplex kobner HPO C0018991 Paralysis one side of body C0022660 Kidney failure, acute HSDN C3641755 Have constipation C3665624 Serum calcium below normal HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0020456 Hyperglycemia HSDN C0232943 Metromenorrhagia C0595904 Menses irregular with excessive bleeding UMLS C4085211 Pain distress question C0751792 Trauma, nervous system HSDN C0242936 Center pain C0161410 Accessory nerve injuries HSDN C0035078 Failure kidney C2930957 Hantavirosis OrphaNet|MalaCards C0004134 Dyssynergia C0342281 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus OrphaNet|MalaCards C0398650 Idiopathic thrombocytopenia purpura C0517555 Venous thrombosis after immobility HSDN C4084766 Vomiting C0017612 Glaucoma, open-angle HSDN C4042891 Sleep wake disorders C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0042963 Symptoms vomiting C0556346 Binge drinking HSDN C3146279 Coma C1306571 Hepatic insufficiency HSDN C0036572 Convulsion C0023241 Legionnaires' disease HSDN C0026821 Cramp C0679360 Foodborne disease HSDN C0004134 Dyssynergia C0302148 Blood clot HSDN C4084773 Bothered by weight gain C0205788 Histiocytoid hemangioma HSDN C0013395 Indigestion C0014591 Epistaxis UMLS C0034151 Hyperglobulinemic purpura C0002874 Aplastic anemia HSDN C4084788 Have dizziness C0027666 Neoplasms, radiation-induced HSDN C2919142 Short stature adverse event C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C4085661 Usual severity nausea C0151740 Intracranial hypertension HSDN C1963071 Back pain adverse event C0026946 Mycoses HSDN C4085222 Nausea C0001314 Acute disease HSDN C1963237 Insomnia adverse event C2931859 Acquired cjd MalaCards C0019825 Voice hoarseness C0007137 Squamous cell carcinoma HSDN C0018784 Deafness sensorineural C0040053 Thrombosis HSDN C0240735 Personality change C0751208 Juvenile huntington disease MalaCards C0015230 Exanthem C1836284 Epidermolysis bullosa simplex with migratory circinate erythema OrphaNet|HPO C0038002 Spleen enlargement C0043208 Wolman disease OrphaNet|HPO C3665346 Loss sight C1869114 Weill-marchesani syndrome, autosomal recessive MalaCards C0424755 Fever symptoms C0022735 Klinefelter syndrome HSDN C3641756 Have diarrhea C0023794 Lipoidosis HSDN C0022660 Acute kidney failure C1856143 Hemolytic uremic syndrome, typical MalaCards C0002622 Amnesias C0016542 Foreign body HSDN C0003469 Anxiety disorder C2931246 Chromosome 17, trisomy 17p11 2 OrphaNet|HPO|MalaCards C0012833 Dizzy C0026780 Mumps HSDN C4085548 Usual severity dizziness C0236736 Cocaine-related disorders HSDN C4085211 Pain distress question C0520720 Cyst nerve root HSDN C0018834 Brash C0751666 Canavan disease, infantile OrphaNet|HPO|MalaCards C4084784 Diarrhea C0001139 Acinetobacter infection HSDN C0700078 Deep tendon reflex decrease C4014942 Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia MalaCards C4085661 Usual severity nausea C0022890 Labyrinthine disorder HSDN C1963087 Constipation adverse event C0021603 Sleep initiation and maintenance disorders HSDN C1963087 Constipation adverse event C2931294 Wiedemann grosse dibbern syndrome MalaCards C4085211 Pain distress question C0021295 Infant, premature, diseases HSDN C0010200 Cough symptom C0004096 Asthma DiseaseOntology|MalaCards C0022346 Yellow skin C2984330 Chagas disease pathway HSDN C4085210 Usual severity pain C0021841 Intestinal neoplasms HSDN C0038002 Spleen enlargement C0024748 Alpha-mannosidosis OrphaNet|HPO C1963086 Confusion adverse event C4050613 Anxiety scale (basc-2) HSDN C0018784 Deafness sensorineural C0001175 Acquired immunodeficiency syndrome HSDN C0700590 Diaphoresis excessive C0206042 Fatal familial insomnia HPO|UMLS C0860603 Anxiety symptom C0393639 Hashimoto's encephalitis MalaCards C0010200 Cough symptom C0862779 Stage iiia adenosquamous cell carcinoma of lung UMLS C0398650 Idiopathic thrombocytopenia purpura C2937358 Cerebral hemorrhage HSDN C4084784 Diarrhea C0036262 Sarcoptic itch HSDN C1963093 Dizziness adverse event C0036421 Systemic scleroderma HSDN C1549543 Administration method - pain C0022570 Keratitis dentritic HSDN C2984058 Have pain C1456784 Paranoia HSDN C4085211 Pain distress question C0017919 Glycogen storage disease HSDN C1963091 Diarrhea adverse event C0025149 Medulloblastoma HSDN C0018772 Deafness C1837501 Microcephaly, primary autosomal recessive, 5 MalaCards|HPO C4084784 Diarrhea C0206624 Hepatoblastoma MalaCards C4042891 Sleep wake disorders C2984572 Malaria pathway HSDN C2911645 Weight loss adverse event C0436596 On examination - apathetic HSDN C0000737 Abdomen pain C0085183 Neoplasms, second primary HSDN C2237041 Shox gene with short stature C3150940 Chromosome 2q31.1 duplication syndrome MalaCards C0152116 Torticollis spasmodic C0809991 Other hereditary and degenerative nervous system conditions UMLS C0030554 Abnormal sensation C0009241 Cognition disorders HSDN C0042798 Vision dim C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0339143 Thyroid associated opthalmopathies HSDN C1963170 Hypothermia adverse event C0035410 Rhabdomyolysis HSDN C0034155 Thrombotic thrombocytopenic purpura C0011570 Mental depression HSDN C0424755 Fever symptoms C0024232 Lymphatic metastasis HSDN C0042798 Vision dim C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards C0036572 Convulsion C0006147 Breast fed HSDN C3539022 Pelvic pain decreasing in severity C0037397 Behavior social HSDN C0036572 Convulsion C0243050 Cardiovascular abnormalities HSDN C4084767 Bothered by vomiting C0162565 Acute intermittent porphyria MalaCards|HSDN|HPO C0042963 Symptoms vomiting C2746068 Congenital idiopathic intestinal pseudoobstruction HPO|UMLS C1549543 Administration method - pain C0032586 Polyradiculopathy HSDN C2237041 Shox gene with short stature C1832817 Klippel-feil deformity, conductive deafness, and absent vagina OrphaNet|MalaCards C0085636 Light sensitivity C0043395 Yellow fever MalaCards C1963184 Nystagmus adverse event C2749049 Corneal dystrophy, endothelial, x-linked MalaCards C0013604 Edematous C1306577 Dies patient HSDN C0020615 Hypoglycemia nos C0342749 Glycogen storage disease ic MalaCards|HPO C2911645 Weight loss adverse event C0206702 Klatskin tumor MalaCards C1963093 Dizziness adverse event C1968848 Epilepsy, familial mesial temporal lobe MalaCards C1963065 Apnea adverse event C0003467 Anxiety HSDN C0522224 Palsied C0024143 Lupus nephritis HSDN C0023014 Developmental disorder language C0036346 Schizophrenia, childhood HSDN C4084802 Usual severity diarrhea C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0007772 Intracranial arteriovenous malformation HSDN C0231528 Muscle pain generalized C0343208 Essential mixed cryoglobulinemia OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0037274 Dermatologic disorders HSDN C4084774 Have weight loss C0376545 Hematologic neoplasms HSDN C0476300 Suppressed urine secretion C0028961 Oliguria UMLS C4084769 Vomiting frequency C0018571 Hand injury HSDN C4084727 Cough frequency C0027439 Nasopharyngeal neoplasms HSDN C0009460 Communication impairment C0006109 Brain damage, chronic HSDN C0427068 Legs weakness C1855346 Mast syndrome MalaCards|HPO C4084788 Have dizziness C0161409 Cochlear nerve damage HSDN C0030193 Sense of pain C0032966 Complication, neoplastic pregnancy HSDN C0085642 Asphyxia reticularis C0282607 Vascular neoplasms HSDN C2936821 Spinal cerebrospinal fluid leak C0025289 Meningitis HSDN C0000737 Abdomen pain C2004491 Cicatrix HSDN C2315100 Pediatric failure to thrive C0220987 Hereditary orotic aciduria MalaCards C4084775 Usual severity weight loss C0302363 Bang disease MalaCards C0012569 Double vision C0149925 Small cell carcinoma of lung HSDN C4084769 Vomiting frequency C1563215 Powassan encephalitis virus infection MalaCards C3463815 Feel fatigue C0948089 Acute coronary syndrome HSDN C4084724 Usual severity constipation C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C0848332 Abnormal skin spots C0302295 Eruptions UMLS C0858567 Phonation difficulty C1527344 Dysphonia UMLS C4049644 Depression C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C1959629 Seizure adverse event C1838163 Osler-rendu-weber syndrome 2 MalaCards C0518090 Frequency of pain question C1963119 Stomach ulcer adverse event HSDN C4084776 Weight loss C0015328 Behavior, exploratory HSDN C0018681 Headache, cephalalgia C0014118 Endocarditis HSDN C0038002 Spleen enlargement C0349653 Congenital disorder of glycosylation type 1a MalaCards C0241210 Speaking delay C3151462 Mental retardation, autosomal recessive 14 MalaCards C4084769 Vomiting frequency C0282207 Cronkhite-canada syndrome MalaCards C3641756 Have diarrhea C0037930 Spinal cord neoplasms HSDN C4084769 Vomiting frequency C0042345 Varicosity HSDN C4084725 Usual severity cough C3809651 Infantile liver failure syndrome 2 MalaCards C3463815 Feel fatigue C1510412 Pseudoaneurysm HSDN C0012833 Dizzy C1636667 Disorder characterized by eosinophilia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004352 Autistic disorder HSDN C0010200 Cough symptom C0038454 Cerebrovascular accident HSDN C0015970 Fever unknown origin C0919267 Ovarian neoplasm HSDN C1579931 Depressed - symptom C1846707 Spinocerebellar ataxia 17 MalaCards|HPO C0019214 Hepatosplenomegaly C1850126 Osteopetrosis, mild autosomal recessive form MalaCards|HPO C2911645 Weight loss adverse event C1720777 Functional laterality HSDN C1384666 Decreased hearing C0042769 Virus diseases HSDN C4084724 Usual severity constipation C1855923 Hyperphosphatasia with mental retardation MalaCards|HPO C2126180 Anal pain accompanied by bleeding C0019080 Hemorrhage UMLS C0027796 Neuralgias C0002949 Aneurysm, dissecting HSDN C3163620 Hypotension adverse event C0431716 Nephronophthisis - medullary cystic disease MalaCards C1963087 Constipation adverse event C0030567 Parkinson disease MalaCards C0851578 Disorder sleep C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards C0012569 Double vision C0033375 Prolactinoma MalaCards|HSDN|HPO C0039070 Collapse fleeting C0086543 Cataract nos HSDN C0518090 Frequency of pain question C0031099 Periodontitis HSDN C0010200 Cough symptom C0005592 Bird fancier's lung DiseaseOntology|MalaCards C0018777 Deafness, conductive C1275078 Acrocephalopolysyndactyly type 2 HPO C0043094 Weight gain C0042344 Varicose ulcer HSDN C0013390 Cramps menstrual C0013418 Abnormal labor HSDN C0151786 Weakness muscle C0265345 Lymphedema distichiasis syndrome OrphaNet|HPO|MalaCards C0020305 Fetal edema C0242621 Isochromosomes HSDN C0020505 Excessive eating C0011265 Presenile dementia HSDN C3463815 Feel fatigue C0003047 Animal disease HSDN C0016204 Fart C0151744 Myocardial ischemia HSDN C1963087 Constipation adverse event C0796561 Melanoma vaccines HSDN C0746674 Muscle weakness generalized C1854106 Inclusion body myopathy 3, autosomal dominant HPO|UMLS C3815497 Cough C0013473 Eating disorders HSDN C2096293 Ent surgical result ear vertigo C0018799 Heart diseases HSDN C3539889 Pelvic pain increasing in severity C2911643 Encounter due to family history of osteoporosis HSDN C1069915 Vertigo C0026782 Mumps vaccine HSDN C0232513 Premature tooth loss C3549874 Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly MalaCards C0030193 Sense of pain C1299919 Enteric coccidiosis HSDN C0401149 Constipation chronic C1846044 Adrenomyodystrophy MalaCards C0242936 Center pain C0037073 Sigmoid neoplasms HSDN C0040034 Thrombocytopenia C1844663 Islets of langerhans, absence of HPO C4085548 Usual severity dizziness C0001973 Alcoholic intoxication, chronic HSDN C0018681 Headache, cephalalgia C2984330 Chagas disease pathway HSDN C0042571 Vertigo subjective C3554047 Ventricular tachycardia, catecholaminergic polymorphic, 4 MalaCards C0270948 Neurogenic muscular atrophy C1853247 Spastic paraplegia 31, autosomal dominant MalaCards|HPO C2242996 Tingling C0021449 Abuse inhalant HSDN C2919142 Short stature adverse event C2936861 Cortisol 11-beta-ketoreductase deficiency MalaCards C0011570 Monopolar depression C0085209 Bovine spongiform encephalitis MalaCards C0270948 Neurogenic muscular atrophy C3250443 Myotonic dystrophy 1 MalaCards C3641756 Have diarrhea C0206617 Cardiovirus infections HSDN C0221752 Rbc urine C0023195 Lecithin acyltransferase deficiency OrphaNet C1384666 Decreased hearing C0032964 Pregnancy complications, hematologic HSDN C4084767 Bothered by vomiting C0010356 Cross infection HSDN C3203358 Alveolar hypoventilation C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0013395 Indigestion C0015927 Intrauterine fetal demise HSDN C4084723 Constipation C0016470 Food allergy HSDN C1962972 Proteinuria adverse event C0035229 Respiratory insufficiency HSDN C1963086 Confusion adverse event C0037274 Dermatologic disorders HSDN C0042514 Ventricular tachycardia C0264903 Premature ventricular complex multifocal MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0002950 Aneurysms inflammatory HSDN C4085548 Usual severity dizziness C0006434 Burn injury HSDN C0020458 Hyperhydrosis C1720189 Episodic ataxia MalaCards C0013604 Edematous C0242422 Parkinsonian disorders HSDN C2242996 Tingling C0042345 Varicosity HSDN C4084766 Vomiting C0006118 Brain neoplasms HSDN C0008031 Pain chest C0011127 Pressure ulcer HSDN C0040485 Wryneck C4084909 Depression subordinate domain HSDN C1962972 Proteinuria adverse event C0268381 Primary amyloidosis OrphaNet|MalaCards C0039070 Collapse fleeting C0035242 Respiratory tract diseases HSDN C0231528 Muscle pain generalized C0023529 Leukomalacia, periventricular HSDN C0024032 Birth weight subnormal C1859405 Bowen-conradi syndrome MalaCards|HPO C0013604 Edematous C0242172 Pelvic inflammatory disease HSDN C4085211 Pain distress question C0011989 Camurati-engelmann syndrome HSDN C1961131 Cough adverse event C0026769 Multiple sclerosis HSDN C0221752 Rbc urine C0037054 Sickle cell trait MalaCards C0085636 Light sensitivity C2930674 Babesioses, human MalaCards C3815497 Cough C2586211 Thrombosis of blood vessel HSDN C0013362 Dysarthrias C0018523 Hallervorden-spatz syndrome MalaCards|HSDN|HPO C1963184 Nystagmus adverse event C2930798 Alexanders leukodystrophy MalaCards C3641756 Have diarrhea C0020456 Hyperglycemia HSDN C0018784 Deafness sensorineural C0005818 Blood platelet disorders HSDN C4084802 Usual severity diarrhea C0750394 Wbc low HSDN C0522224 Palsied C0521542 Brainstem infarct HSDN C0522224 Palsied C1963119 Stomach ulcer adverse event HSDN C0030193 Sense of pain C0752242 Limitus, hallux HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0428478 Serum triglycerides raised HSDN C1263846 Attention deficit disorder with hyperactivity C0751120 Benign infantile myoclonic epilepsy OrphaNet|MalaCards C0206146 Myocardial stunning C0006110 Brain death HSDN C0237326 Defecation pain C0042781 Visceral myopathy MalaCards C3539892 Pelvic pain in front C0038478 Struma ovarii HSDN C1557397 Adverse event associated with pain C0018566 Congenital hand deformities HSDN C0012833 Dizzy C0020476 Hyperlipoproteinemias HSDN C4085661 Usual severity nausea C0007133 Carcinoma, papillary HSDN C0349588 Stature short C2678039 Mental retardation, x-linked, syndromic 9 MalaCards C1961131 Cough adverse event C1535917 Nipah virus infection MalaCards C4084784 Diarrhea C0162557 Liver failure, acute HSDN C3887873 Hearing loss C0011168 Deglutition disorders HSDN C2130177 Number of weeks into pregnancy when bleeding noted C3163625 Vaginal bleeding during pregnancy UMLS C2242996 Tingling C0037744 Perceptual spatial orientation HSDN C1260880 Nasal drip C0279748 Lymphoepithelioma, nasopharyngeal UMLS C0018965 Blood urine C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C0013404 Respiratory difficulty C4225334 Autoimmune interstitial lung, joint, and kidney disease UMLS C0000727 Abdomen acute C0007193 Cardiomyopathy, dilated HSDN C4084774 Have weight loss C0029295 Oropharyngeal neoplasms HSDN C0036572 Convulsion C0278192 Gustatory partial seizure UMLS C3178766 Nociceptive pain C0043145 Whiplash HSDN C2237041 Shox gene with short stature C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C1961131 Cough adverse event C1836929 Emanuel syndrome MalaCards C2919142 Short stature adverse event C1858079 Osteoarthritis with mild chondrodysplasia HPO C4085317 Diarrhea frequency C1962971 Myocarditis adverse event HSDN C0878773 Bladder hyperactive C0270328 Diurnal enuresis HSDN C2919142 Short stature adverse event C3697269 15q24 microdeletion OrphaNet|HPO C4084775 Usual severity weight loss C0042035 Urination disorders HSDN C0576433 Excessive growth of leg hair C0020555 Hypertrichosis UMLS C0020305 Fetal edema C0085132 Mucopolysaccharidosis vii OrphaNet|HPO C0018772 Deafness C3540852 Rickets, x-linked hypophosphatemic MalaCards|HPO C2315100 Pediatric failure to thrive C0342273 Transient neonatal diabetes mellitus MalaCards C3641756 Have diarrhea C0030524 Paratuberculosis HSDN C0018775 Hearing loss bilateral C1762616 Meningioma, benign, no icd-o subtype HSDN C4084725 Usual severity cough C0007282 Carotid stenosis HSDN C2919142 Short stature adverse event C1868508 Kosenow syndrome MalaCards C0427008 Stiffness C0796126 Aicardi-goutieres syndrome 1 MalaCards C1557397 Adverse event associated with pain C0008372 Intrahepatic cholestasis HSDN C1962972 Proteinuria adverse event C0032708 Disorders of porphyrin metabolism HSDN C4084767 Bothered by vomiting C0014549 Tonic-clonic epilepsy HSDN C3829611 Nausea frequency C0036916 Sexually transmitted diseases HSDN C0013604 Edematous C1550672 Specimen type - ulcer HSDN C0475858 Pruritis generalized C0748035 Pruritus chronic UMLS C0002963 Angina variant C0948089 Acute coronary syndrome HSDN C0013604 Edematous C2240378 Cleft palate on exam HSDN C0018520 Breath odor C0027030 Maggot infection HSDN C0003811 Cardiac rhythm disturbance C2749345 Refsum disease, adult, 1 HPO C4084802 Usual severity diarrhea C0237873 Physiological sexual disorders HSDN C1557397 Adverse event associated with pain C0010633 Cystadenoma HSDN C2984058 Have pain C0042258 Vaginal neoplasms HSDN C4084768 Usual severity vomiting C0003615 Appendicitis DiseaseOntology|HSDN|MalaCards C0000727 Abdomen acute C0001430 Adenoma HSDN C0015676 Mental fatigue C0042830 Perception visual HSDN C1963093 Dizziness adverse event C0022658 Kidney diseases HSDN C1263846 Attention deficit disorder with hyperactivity C0162309 Adrenoleukodystrophy OrphaNet|HPO|MalaCards C0034150 Skin purpura C1856447 Bernard soulier syndrome, type b HPO C1279888 Proteinuria of undiagnosed cause C0019163 Hepatitis b HSDN C4084802 Usual severity diarrhea C3149378 Immunodeficiency, common variable, 1 MalaCards|HPO C2032396 Pelvic pain on the right C0018799 Heart diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0036220 Kaposi sarcoma HSDN C0917816 Deficiency mental C0574085 3-methylglutaconic aciduria type 4 OrphaNet|MalaCards C4084766 Vomiting C2711591 Infection by anisakidae HSDN C0231528 Muscle pain generalized C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0009024 Clonus C3281029 Rigidity and multifocal seizure syndrome, lethal neonatal MalaCards|UMLS C4084802 Usual severity diarrhea C1962983 Cataract adverse event HSDN C0018926 Emesis bloody C0004096 Asthma HSDN C0424755 Fever symptoms C0027743 Nerve compression syndrome HSDN C0349588 Stature short C1852576 Copper deficiency, familial benign OrphaNet|MalaCards C0231807 Dyspnea exertional C0162872 Aortic aneurysm, thoracic MalaCards C0028738 Nystagmus C0175713 Aicardi's syndrome MalaCards C3539893 Pelvic pain occurs with intercourse C0033873 Psychiatry HSDN C0007758 Cerebellar ataxia C0393535 Drug-induced cerebellar ataxia UMLS C4085549 Dizziness C0020476 Hyperlipoproteinemias HSDN C4085549 Dizziness C0036421 Systemic scleroderma HSDN C2911645 Weight loss adverse event C0035358 Retroperitoneal neoplasm HSDN C3541349 Syncope C0026769 Multiple sclerosis HSDN C0013378 Dysgensia C0376175 Bell palsy HSDN C2029884 Hearing loss by exam C0007795 Diffuse cerebral sclerosis of schilder MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1854336 Paragangliomas 3 MalaCards C0030552 Paralysis partial C0032708 Disorders of porphyrin metabolism MalaCards C3641756 Have diarrhea C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C0178417 Anhedonia C2350521 Gustatory perception HSDN C3829611 Nausea frequency C0036690 Septicemia HSDN C0426579 Anorexia symptom C1285666 Drinking behavior HSDN C3641756 Have diarrhea C1504665 Products used to treat diabetic ketoacidosis HSDN C3541349 Syncope C2609414 Acute kidney injury HSDN C0033774 Skin pruritus C1000587 Pemphigus HSDN C0476273 Distress respiratory C0796070 Microphthalmia, syndromic 7 MalaCards C0232466 Feeding difficulty C2675336 Duplication 15q11-q13 syndrome MalaCards C0015672 Decreased energy C0004114 Astrocytoma HSDN C1279888 Proteinuria of undiagnosed cause C0017181 Gastrointestinal hemorrhage HSDN C0015672 Decreased energy C0014849 Esophageal and gastric varices HSDN C0242936 Center pain C0031485 Phenylketonurias HSDN C0018681 Headache, cephalalgia C0393751 Cold stimulus induced headache UMLS C0030193 Sense of pain C0019554 Dislocate hip HSDN C4084726 Distress cough C0549472 Pneumonia, cholesterol MalaCards C4085211 Pain distress question C0014556 Epilepsy, temporal lobe HSDN C4085210 Usual severity pain C0032087 Plant poisoning HSDN C0018784 Deafness sensorineural C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C1557397 Adverse event associated with pain C0015558 Fallopian tube neoplasms HSDN C3539890 Pelvic pain causes awakening at night C0038478 Struma ovarii HSDN C2024893 Cardiovascular surgery result: fatigue C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C0013604 Edematous C0585442 Osteosarcoma of bone HSDN C4085210 Usual severity pain C0024131 Lupus vulgaris HSDN C4085211 Pain distress question C0036202 Sarcoidosis HSDN C0018772 Deafness C3280011 Brittle cornea syndrome 2 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0085396 Neisseriaceae infections HSDN C1557397 Adverse event associated with pain C0017920 Glycogen storage disease type i HSDN C0009421 Comatose C0005967 Bone neoplasms HSDN C0027066 Myoclonic jerking C2931859 Acquired cjd MalaCards C0427055 Face weakness C1833373 Inclusion body myopathy, autosomal recessive MalaCards|HPO C0013604 Edematous C0039520 Tenosynovitis HSDN C2024878 Cardiovascular surgery result: dyspnea C3463992 Epileptic encephalopathy, early infantile, 1 MalaCards C0027497 Queasy C0009450 Disease caused by microorganism HSDN C0018784 Deafness sensorineural C0011581 Depressive disorder HSDN C0003811 Cardiac rhythm disturbance C1864668 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4 MalaCards|HPO C2203646 Jaundice C0265275 Jeune thoracic dystrophy MalaCards C0243026 Generalized infection C0085110 Severe combined immunodeficiency OrphaNet|MalaCards C1579931 Depressed - symptom C0001529 Dercum disease OrphaNet|MalaCards C3815497 Cough C0038940 Surgical wound dehiscence HSDN C4085211 Pain distress question C1299919 Enteric coccidiosis HSDN C0522224 Palsied C0021400 Influenza HSDN C3641756 Have diarrhea C2936917 Infantile polyarteritis MalaCards C0013404 Respiratory difficulty C0152938 Secondary pneumonic plague DiseaseOntology|MalaCards C0151786 Weakness muscle C0035309 Retinal diseases HSDN C0040485 Wryneck C0021400 Influenza HSDN C0234146 Absent reflex C0043459 Zellweger syndrome HPO C0013604 Edematous C1865270 Bartter syndrome, type 4a HPO C0522224 Palsied C0011175 Dehydration HSDN C0033774 Skin pruritus C2984299 Asthma pathway HSDN C1384666 Decreased hearing C0011849 Diabetes mellitus HSDN C0023012 Delay language C0241932 X-linked hypogammaglobulinemia HPO C2237041 Shox gene with short stature C3150803 Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia MalaCards|HPO C2984058 Have pain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0002170 Alopecia disorders C0878684 Short syndrome MalaCards C0019209 Large liver C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0018681 Headache, cephalalgia C0016665 Fracture, nos with nonunion HSDN C4084774 Have weight loss C0033817 Pseudomonas infections HSDN C0030193 Sense of pain C0001118 Acid base imbalance HSDN C0424755 Fever symptoms C0376300 Dengue shock syndrome OrphaNet|MalaCards C2984058 Have pain C0026718 Mucormycosis HSDN C0151889 Reflexes tendon increased C0009207 Cockayne syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0036983 Septic shock HSDN C0011991 Loose stools C0006105 Brain abscess HSDN C4084897 Sleep disturbance subordinate domain C3151140 Pontocerebellar hypoplasia, type 2d HPO C3815497 Cough C0041326 Pleural tuberculosis HSDN C0700072 Encounter due to stillbirth C1859148 Chondrodysplasia, blomstrand type HPO C3541349 Syncope C4015710 Tenorio syndrome MalaCards C0012833 Dizzy C0037274 Dermatologic disorders HSDN C0013604 Edematous C0022602 Actinic keratosis HSDN C2984057 Have nausea C0085111 Ankle injury HSDN C2029884 Hearing loss by exam C1868311 Piebald trait neurologic defects MalaCards C0518090 Frequency of pain question C0869332 Of water deprivation HSDN C0013404 Respiratory difficulty C0460137 Push down or depress HSDN C0027497 Queasy C0206696 Carcinoma, signet ring cell HSDN C0015970 Fever unknown origin C2049812 Infection due to other organisms UMLS C0007814 Cerebrospinal fluid otorrhea C0029440 Osteoma HSDN C2984058 Have pain C0241158 Cicatrix skin HSDN C0151311 Cranial nerve palsy C0036421 Systemic scleroderma MalaCards C1549543 Administration method - pain C0014849 Esophageal and gastric varices HSDN C0011991 Loose stools C0026764 Multiple myeloma HSDN C1860844 Sparse, thin hair C0026363 Mohr-claussen syndrome MalaCards C0008031 Pain chest C0001580 Adolescent behavior HSDN C0028961 Urine output decreased C3888018 Congenital hyperinsulinism HSDN C0020305 Fetal edema C3887662 Intraspinal neoplasm HSDN C0241210 Speaking delay C2677567 Dystonia 16 (disorder) MalaCards|HPO C4084766 Vomiting C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0024032 Birth weight subnormal C1858538 Blepharophimosis with facial and genital anomalies and mental retardation MalaCards C0426579 Anorexia symptom C2370841 Convalescence; treatment HSDN C1549543 Administration method - pain C2936664 Acquired hypogammaglobulinemia HSDN C0917816 Deficiency mental C1846796 Anauxetic dysplasia MalaCards|HPO C0008031 Pain chest C1546654 Specimen source codes - granuloma HSDN C0030193 Sense of pain C0011432 Dentin hypersensitivity HSDN C2984057 Have nausea C0162872 Aortic aneurysm, thoracic HSDN C0037316 Not enough sleeping C0085541 Epilepsy, frontal lobe HSDN C0349588 Stature short C3150970 Noonan syndrome 7 MalaCards|HPO C0042964 Anticipatory vomiting C0018467 Habituation, psychophysiologic HSDN C0004604 Pain back C0000833 Abscess HSDN C4085862 Bothered by nausea C1546654 Specimen source codes - granuloma HSDN C0018991 Paralysis one side of body C0242422 Parkinsonian disorders HSDN C0004134 Dyssynergia C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy HPO|UMLS C4084768 Usual severity vomiting C0403447 Chronic kidney insufficiency HSDN C0232466 Feeding difficulty C0020681 Sleep-related respiratory failure MalaCards C2024878 Cardiovascular surgery result: dyspnea C0002170 Alopecia HSDN C1263846 Attention deficit disorder with hyperactivity C1861129 Takao vcf syndrome HPO C1963091 Diarrhea adverse event C1970712 Multiple endocrine neoplasia, type iv OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C3829611 Nausea frequency C0003493 Aortic diseases HSDN C0016204 Fart C0012242 Digestive system disorders HSDN C2984058 Have pain C1510502 Oxyphilic adenoma HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0751674 Lymphangioleiomyomatosis OrphaNet|HSDN|HPO|MalaCards C0015469 Facial paralysis C1832399 Charcot-marie-tooth disease, type 4b1 MalaCards|HPO C0000727 Abdomen acute C0162533 Porphyrias, hepatic HSDN C3539895 Pelvic pain occurs with bowel movement C0029456 Osteoporosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0018671 Head and neck neoplasms HSDN C1962972 Proteinuria adverse event C0036974 Shock HSDN C0271215 Blindness legal C3495554 Homocarnosinase deficiency MalaCards C0022346 Yellow skin C1336208 Stage iiia carcinoma of liver cells UMLS C4085211 Pain distress question C0020428 Hyperaldosteronism HSDN C0042928 Paralysis vocal cord C1548578 Location characteristic id - smoking HSDN C0004134 Dyssynergia C0152164 Cyclical vomiting syndrome (disorder) MalaCards C0022346 Yellow skin C0027932 Neurotic disorders HSDN C0242936 Center pain C0679360 Foodborne disease HSDN C3641756 Have diarrhea C0162539 Igg deficiency HSDN C1963180 Neck pain adverse event C1881674 Medical device emits smoke HSDN C0013404 Respiratory difficulty C0264342 Bronchitis plastic UMLS C0557874 Global developmental delay C2931010 Congenital disorder of glycosylation type 2e MalaCards C4084776 Weight loss C0036992 Short bowel syndrome HSDN C0020903 Illusion C1522475 Intradermal route of drug administration HSDN C1963170 Hypothermia adverse event C1261473 Sarcoma HSDN C1963137 Hydrocephalus adverse event C0795841 Jacobsen distal 11q deletion syndrome MalaCards C4050613 Anxiety C1868681 Dystonia 12 HPO C4084776 Weight loss C0007137 Squamous cell carcinoma HSDN C0018784 Deafness sensorineural C0007820 Cerebrovascular disorders HSDN C1549543 Administration method - pain C0206711 Pilomatrixoma HSDN C0018772 Deafness C0017205 Gaucher disease MalaCards C1557397 Adverse event associated with pain C0497573 Condylomata acuminata in women HSDN C2911645 Weight loss adverse event C1547044 Kind of quantity - smell HSDN C0004604 Pain back C0013182 Drug allergy HSDN C3887873 Hearing loss C0002871 Anemia HSDN C0000737 Abdomen pain C0041310 Endocrine tuberculoses HSDN C0043144 Wheeze C0004031 Aspergillosis, allergic bronchopulmonary DiseaseOntology|MalaCards C1963170 Hypothermia adverse event C0037933 Spinal diseases HSDN C0009763 Conjunctiva inflammation C2931873 Juvenile cranial arteritis MalaCards C4084773 Bothered by weight gain C0038579 Substance abuse, intravenous HSDN C1145670 Failure respiratory C3809971 Asparagine synthetase deficiency MalaCards C1963065 Apnea adverse event C0860603 Anxiety symptoms HSDN C2032396 Pelvic pain on the right C2936631 Complaint, subjective health HSDN C1962972 Proteinuria adverse event C0005396 Bile duct neoplasms HSDN C0150045 Urinary incontinence urge C0600041 Infective cystitis HSDN C1963093 Dizziness adverse event C0003467 Anxiety HSDN C1963091 Diarrhea adverse event C1135821 Mortality syndrome, spiking HSDN C0234518 Speech slurred C0268226 Type i mucolipidosis OrphaNet|HPO C2073625 X-ray of chest: pleural effusion C0149951 Ovarian fibromata OrphaNet|MalaCards C4084776 Weight loss C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0413252 Hypothermia due to exposure C0026640 Mouth neoplasms HSDN C1557397 Adverse event associated with pain C0021141 Inappropriate adh syndrome HSDN C1963086 Confusion adverse event C1290398 Cerebral arterial aneurysm HSDN C0030193 Sense of pain C0036918 Sexually transmitted diseases, viral HSDN C0013390 Cramps menstrual C1720861 Familial partial lipodystrophy, type 3 MalaCards|HPO C0013604 Edematous C0007196 Restrictive cardiomyopathy HSDN C0035232 Diaphragmatic paralysis C0425045 Sudden infant death HSDN C4084742 Bothered by night sweats C0349535 Carcinoid tumor of intestine MalaCards C3641755 Have constipation C3178970 Entrapment, pudendal nerve MalaCards C0151889 Reflexes tendon increased C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C0019209 Large liver C0342720 Adenosylcobalamin synthesis defect MalaCards C0003467 Angst C2936741 Syndrome xxyy OrphaNet|MalaCards C0917816 Deficiency mental C0013080 Down syndrome OrphaNet|HPO|MalaCards C0034933 Abnormal reflexes C0700208 Acquired scoliosis HSDN C0009806 Constipate C0278474 Stage i colon carcinoma UMLS C0026821 Cramp C0032787 Postoperative complications HSDN C0521654 Motor deficit C2751584 Neurodegeneration due to cerebral folate transport deficiency MalaCards C0085602 Polydypsia C0021125 Impulsive behavior HSDN C0451941 Itch scrotum C1290026 Disease of skin and/or subcutaneous tissue of trunk UMLS C0030193 Sense of pain C0005974 Bone resorption HSDN C4085210 Usual severity pain C0242350 Erectile dysfunction HSDN C4084723 Constipation C1258104 Diffuse scleroderma HSDN C2984058 Have pain C0001349 Acute-phase reaction HSDN C0043068 Friderichsen-waterhouse syndrome C0010481 Cushing syndrome HSDN C2984057 Have nausea C1299624 Postural orthostatic tachycardia syndrome HSDN C0000737 Abdomen pain C0563150 Catastrophization HSDN C0036572 Convulsion C0795887 Chromosome xp21 deletion syndrome MalaCards C0085606 Urination urgency C1849128 Spastic paraplegia 15, autosomal recessive MalaCards|HPO C0149651 Clubbing C0023760 Lip diseases MalaCards C3641756 Have diarrhea C0042214 Vaccinia HSDN C0042024 Urine incontinence C0007097 Carcinomas HSDN C1963091 Diarrhea adverse event C0206698 Cholangiocarcinoma HSDN C0020578 Hyperventilate C0033845 Pseudotumor cerebri HSDN C0520904 Postoperative nausea C0032787 Postoperative complications UMLS C4085210 Usual severity pain C1552527 Clinic / center - developmental disabilities HSDN C0242670 Chronic vegetative state C0151699 Intracranial hemorrhages HSDN C3829611 Nausea frequency C0004610 Bacteremia HSDN C4084773 Bothered by weight gain C0039538 Teratoma HSDN C1963086 Confusion adverse event C1458155 Mammary neoplasms HSDN C4085548 Usual severity dizziness C0007131 Non-small cell lung carcinoma HSDN C0162298 Stiffness joints C0265224 Freeman-sheldon syndrome OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0009730 Spinal meningocele HSDN C0012833 Dizzy C0003469 Anxiety disorders HSDN C0242936 Center pain C0024894 Mastitis HSDN C1557397 Adverse event associated with pain C0029421 Osteochondritis dissecans HSDN C0007166 Cardiac output decreased C0022665 Kidney neoplasm HSDN C4049644 Depression C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C0018932 Bright red rectal bleeding C1832940 Juvenile polyposis of stomach HPO C0575081 Abnormal gait C2931617 Bahemuka brown syndrome MalaCards C0557874 Global developmental delay C1845142 Mental retardation, x-linked 91 (disorder) HPO C0015970 Fever unknown origin C0026769 Multiple sclerosis HSDN C2911645 Weight loss adverse event C0238339 Hereditary pancreatitis HSDN C0042963 Symptoms vomiting C0752181 Central nervous system parasitic infections HSDN C2919142 Short stature adverse event C0008928 Cleidocranial dysplasia OrphaNet|HPO|MalaCards C3665347 Vision impaired C0021345 Infectious mononucleosis MalaCards C0019079 Bloody sputum C0026919 Mycobacterium infections, nontuberculous HSDN C0004604 Pain back C0038013 Ankylosing spondylitis MalaCards C1961131 Cough adverse event C0040558 Toxoplasmosis HSDN C0019079 Bloody sputum C0030297 Pancreatic neoplasm HSDN C0013404 Respiratory difficulty C0001175 Acquired immunodeficiency syndrome HSDN|UMLS C0000737 Abdomen pain C0004352 Autistic disorder HSDN C4084767 Bothered by vomiting C0003463 Anus neoplasms HSDN C3641755 Have constipation C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C0221184 Hemianopsia bitemporal C0010276 Craniopharyngioma OrphaNet|HPO|MalaCards C0206146 Myocardial stunning C1145628 Autonomic nervous system disorders HSDN C0000727 Abdomen acute C0041582 Ulcer HSDN C0476273 Distress respiratory C0700635 Strudwick syndrome HPO C0042571 Vertigo subjective C1832475 Deafness, autosomal dominant 11 MalaCards|HPO C4084768 Usual severity vomiting C0015802 Femur fracture HSDN C0000727 Abdomen acute C0022661 Kidney failure, chronic HSDN C0018772 Deafness C0013386 Dyskinesia, drug-induced HSDN C0010038 Corneal opacity disorder C0265221 Walker-warburg congenital muscular dystrophy MalaCards|HPO C3887638 Failure to thrive in infant C0796004 Kabuki make-up syndrome OrphaNet|HPO|MalaCards C0033377 Caudal displacement C2931119 Mehes syndrome OrphaNet|MalaCards C0557874 Global developmental delay C0268228 Neuraminidase 1 deficiency OrphaNet C3887784 Decreased urine output C0018801 Heart failure HSDN C2032395 Pelvic pain on the left C0018199 Granuloma, plasma cell HSDN C0085636 Light sensitivity C1868569 Patterned dystrophy of retinal pigment epithelium MalaCards|HPO C0003862 Pain joint C0152085 Post-dysenteric reactive arthropathy nos MalaCards C4020887 Photodysphoria C0268138 Xeroderma pigmentosum, complementation group d HPO C2024893 Cardiovascular surgery result: fatigue C1691228 Cystic kidney diseases HSDN C2984058 Have pain C0281865 Hip injury HSDN C0022346 Yellow skin C0034184 Pyelocystitis HSDN C0020672 Body temperature decreased C0085096 Peripheral vascular diseases HSDN C0030193 Sense of pain C0007862 Cervico-brachial neuralgia UMLS C1963090 Dehydration adverse event C1449842 Pseudohypoaldosteronism, type i, autosomal dominant HPO C0027498 Nausea vomiting C0341190 Gastritis drug induced UMLS C3641756 Have diarrhea C0037305 Neoplasm, skull HSDN C0231712 Gait waddling C0013264 Muscular dystrophy, duchenne HPO|UMLS C1963087 Constipation adverse event C2713347 7-dehydrocholesterol reductase deficiency MalaCards C0013362 Dysarthrias C0394006 Dysequilibrium syndrome HPO C0034933 Abnormal reflexes C0039144 Syringomyelia HSDN C1963281 Vomiting adverse event C0016952 Galactosemias MalaCards C1384666 Decreased hearing C1863370 Saethre-chotzen syndrome with eyelid anomalies HPO C0037383 Sneeze C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4085317 Diarrhea frequency C0001314 Acute disease HSDN C0019825 Voice hoarseness C3887992 Thyrotropin-releasing hormone deficiency MalaCards C2315100 Pediatric failure to thrive C0020681 Sleep-related respiratory failure MalaCards C0409557 Rubella arthralgia C0035920 Rubella UMLS C2984058 Have pain C0027822 Neurodermatitis HSDN C1963063 Anorexia adverse event C0017178 Gastrointestinal diseases HSDN C0002962 Angina C2945560 Hemolytic HSDN C0013604 Edematous C0033941 Psychoses, substance-induced HSDN C3541349 Syncope C0036323 Schistosomiasis HSDN C0018524 Hallucinate C0043251 Wounds and injuries HSDN C1963281 Vomiting adverse event C0030330 Panniculitis, peritoneal HSDN C1962972 Proteinuria adverse event C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C0413252 Hypothermia due to exposure C0033054 Prenatal exposure delayed effects HSDN C1963071 Back pain adverse event C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0151686 Growth retardation C3277723 Joubert syndrome 12 MalaCards C0036659 Sensation disorder C0525042 Feeding and eating disorders of childhood HSDN C0027497 Queasy C0007297 Car sickness UMLS C0004134 Dyssynergia C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) MalaCards|HPO C0557874 Global developmental delay C1850106 Raine syndrome MalaCards|HPO C0030552 Paralysis partial C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C0020672 Body temperature decreased C0042769 Virus diseases HSDN C0242936 Center pain C0023860 Listeriosis HSDN C0423718 Thalamic pain C1536114 Central pain syndrome UMLS C0003811 Cardiac rhythm disturbance C0544012 Aberfeld's syndrome MalaCards C0020438 Hypercalciuria C0010674 Cystic fibrosis MalaCards|HPO C0034933 Abnormal reflexes C2911643 Encounter due to family history of osteoporosis HSDN C4084767 Bothered by vomiting C0023441 Leukemia, experimental HSDN C0018991 Paralysis one side of body C2937421 Prostatic hyperplasia HSDN C4085210 Usual severity pain C1656583 Rosacea HSDN C0020673 Hypothermia (central) (local) C1720777 Functional laterality HSDN C4084784 Diarrhea C0013922 Embolism HSDN C2237041 Shox gene with short stature C0017205 Gaucher disease MalaCards C3641756 Have diarrhea C1136033 Cutaneous mastocytosis MalaCards C0151686 Growth retardation C3495488 Axenfeld-rieger syndrome HPO C0221752 Rbc urine C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C0004604 Pain back C0018188 Granuloma HSDN C0184567 Pain acute C0016053 Fibromyalgia HSDN C1961131 Cough adverse event C0026764 Multiple myeloma HSDN C0016199 Pain flank C0282609 Bone marrow neoplasms HSDN C1963087 Constipation adverse event C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C4049644 Depression C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0019572 Hairiness C0269995 Galactorrhea associated with childbirth HSDN C4084802 Usual severity diarrhea C0268322 Chester-type porphyria HPO C0012833 Dizzy C0702166 Acne HSDN C1963281 Vomiting adverse event C0013922 Embolism HSDN C1963170 Hypothermia adverse event C1563716 Thyroid dysgenesis HPO C0016382 Cutaneous vascular engorgement C3891449 Peeling skin syndrome 1 MalaCards C0398650 Idiopathic thrombocytopenia purpura C0751674 Lymphangioleiomyomatosis HSDN C4084725 Usual severity cough C0029463 Osteosarcoma HSDN C3665347 Vision impaired C1856143 Hemolytic uremic syndrome, typical MalaCards C0728710 Pupil constriction observed C1418479 Pex7 gene HSDN C4084776 Weight loss C0006840 Candidiasis HSDN C0518090 Frequency of pain question C0040583 Tracheal stenosis HSDN C1321898 Bloody stool C0265031 Hemorrhoid bleeding UMLS C2911645 Weight loss adverse event C0013295 Duodenal ulcer HSDN C0242936 Center pain C0032586 Polyradiculopathy HSDN C2025995 Cellulitis C4048800 Telomeric 22q13 monosomy syndrome MalaCards C3274924 Have been coughing C0038661 Suicide HSDN C0518090 Frequency of pain question C0001815 Primary myelofibrosis HSDN C3898969 Have been vomiting C0038395 Streptococcal infections HSDN C0007758 Cerebellar ataxia C0035305 Retinal detachment HSDN C0851578 Disorder sleep C0005779 Blood coagulation disorders HSDN C4084726 Distress cough C0748164 Pulmonary nodule multiple HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085083 Ovarian hyperstimulation syndrome HSDN C4084725 Usual severity cough C0007194 Hypertrophic cardiomyopathy HSDN C1963065 Apnea adverse event C0018824 Heart valve disease HSDN C4085210 Usual severity pain C0023374 Lesch-nyhan syndrome HSDN C1549543 Administration method - pain C0242172 Pelvic inflammatory disease HSDN C0026838 Spasticity muscle C1000483 Genus anemia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0019285 Diaphragmatic hernia traumatic HSDN C0007758 Cerebellar ataxia C0221036 Acrodermatitis enteropathica HPO|UMLS C0576456 Poor feeding C0265354 Charge syndrome MalaCards C0010200 Cough symptom C0001261 Actinomycosis HSDN C2219981 Fever recurring every few days C0035021 Relapsing fever UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0453996 Tobacco smoking HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0021390 Inflammatory bowel diseases HSDN C0042420 Vasovagal episode C0003811 Cardiac arrhythmia HSDN C0030554 Abnormal sensation C0001197 Acrodermatitis HSDN C0085593 Chill C1709578 Pleural sarcomatoid mesothelioma UMLS C0007398 Catatonic C2586211 Thrombosis of blood vessel HSDN C4042891 Sleep wake disorders C0021361 Female infertility HSDN C0393903 Leg moving painful toe C1527351 Nerve root disorder UMLS C0004134 Dyssynergia C0001175 Acquired immunodeficiency syndrome HSDN C1963154 Renal failure adverse event C2931783 Amelogenesis imperfecta nephrocalcinosis MalaCards C4085317 Diarrhea frequency C0026683 Mucocele HSDN C1963086 Confusion adverse event C0007784 Cerebral hemisphere hemorrhage HSDN C0007758 Cerebellar ataxia C1859568 Bardet-biedl syndrome 10 HPO C0035229 Respiratory function impaired C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C0413252 Hypothermia due to exposure C0033817 Pseudomonas infections HSDN C0027498 Nausea vomiting C1449844 Pseudohypoaldosteronism, type ii OrphaNet|MalaCards C0011206 Delirium acute C0004935 Animal ethology HSDN C0004604 Pain back C0021364 Male infertility HSDN C0162292 Extraocular palsy C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0036221 Mast-cell sarcoma HSDN C1963065 Apnea adverse event C3665624 Serum calcium below normal HSDN C0037763 Spasm C0079744 Diffuse large b-cell lymphoma HSDN C0020672 Body temperature decreased C0017160 Gastroenteritis HSDN C0026838 Spasticity muscle C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO|UMLS C3665492 Pigmentations C3496549 Male germ cell tumor MalaCards C0426579 Anorexia symptom C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0023014 Developmental disorder language C0242387 Mandibulofacial dysostosis HSDN C0042963 Symptoms vomiting C1335316 Pancreatic microcystic adenoma UMLS C0405495 Breast implant pain C0405486 Disorder of breast implant UMLS C0030193 Sense of pain C0008065 Childhood behavior HSDN C4084776 Weight loss C0041296 Tuberculosis OrphaNet|HPO C1279888 Proteinuria of undiagnosed cause C0001430 Adenoma HSDN C0020673 Hypothermia (central) (local) C0007117 Basal cell carcinoma HSDN C4038703 Spasmodic torticollis due to infection C0009450 Disease caused by microorganism UMLS C0027796 Neuralgias C0007873 Uterine cervical neoplasm HSDN C0237326 Defecation pain C1866495 Bartter syndrome, antenatal type 1 HPO C2984057 Have nausea C3839212 Familial hyperaldosteronism type 2 MalaCards C0232466 Feeding difficulty C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0020458 Hyperhydrosis C2931735 Epidermolytic palmoplantar keratoderma vorner type OrphaNet|HPO|MalaCards C0008031 Pain chest C0694545 Chest pain syndrome UMLS C0426579 Anorexia symptom C1527429 Increased blood npn HSDN C4084776 Weight loss C0346303 Thyrotroph adenoma OrphaNet|MalaCards C0237326 Defecation pain C0221043 Liddle syndrome OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0032964 Pregnancy complications, hematologic HSDN C0020450 Hyperemesis gravidarum C0544565 Hyperemesis gravidarum, moderate UMLS C0015300 Ocular proptosis C0264353 Bronchomalacia MalaCards C3665347 Vision impaired C3553951 Peroxisome biogenesis disorder 7b MalaCards C1963170 Hypothermia adverse event C0038436 Post-traumatic stress disorder HSDN C0020305 Fetal edema C0424688 Small head HSDN C0020538 Hbp C0027341 Nail-patella syndrome MalaCards|HPO C0018777 Deafness, conductive C0314657 Genetic predisposition HSDN C0857305 Thrombocytopenia purpura C0022665 Kidney neoplasm HSDN C0018524 Hallucinate C0037361 Olfactory sense HSDN C0233514 Behavior abnormal C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0016199 Pain flank C0027412 Opioid-related disorders HSDN C4085317 Diarrhea frequency C1261473 Sarcoma HSDN C4085210 Usual severity pain C0008373 Cholesteatoma HSDN C0013428 Painful urination C1546533 Specimen source codes - abscess HSDN C0577569 Mass of male genital structure C0017417 Genital neoplasms, male UMLS C0242936 Center pain C0002170 Alopecia HSDN C0020458 Hyperhydrosis C0039483 Giant cell arteritis MalaCards|HPO C0022346 Yellow skin C1963215 Pneumothorax adverse event HSDN C1963091 Diarrhea adverse event C0005779 Blood coagulation disorders HSDN C0023015 Language handicap C0027765 Nervous system disorder HSDN C0013604 Edematous C0042749 Viremia HSDN C3541349 Syncope C0242231 Coronary stenosis HSDN C0518090 Frequency of pain question C0008354 Cholera HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206696 Carcinoma, signet ring cell HSDN C0277799 Fever intermittent C1864997 Majeed syndrome MalaCards|HPO C2911647 Weight gain adverse event C2911243 Encounter due to family history of colonic polyps HSDN C0004604 Pain back C0021359 Infertility HSDN C0002965 Crescendo angina C0027643 Neoplasm recurrence, local HSDN C4084773 Bothered by weight gain C1547044 Kind of quantity - smell HSDN C0221263 Cafe au lait spot C1837475 Insulin-like growth factor i deficiency MalaCards|HPO C1963249 Tinnitus adverse event C0024305 Lymphoma, non-hodgkin HSDN C0030552 Paralysis partial C0268123 Muscle amp deaminase deficiency MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0039128 Syphilis HSDN C1838869 Proximal neurogenic muscle weakness C2678015 Myopathy, reducing body, x-linked, childhood-onset HPO C0022660 Acute kidney failure C0024534 Malaria, cerebral MalaCards C0747245 Paracervical swelling C0746345 Lymphoma nodular large cell UMLS C1527344 Dysphonia C3554447 Dystonia 25 MalaCards C0155502 Vertigo benign positional C0155490 Middle ear cholesteatoma HSDN C0003862 Pain joint C0036205 Sarcoidosis, pulmonary HSDN C0004310 Auditory disorder process C0020936 Imitative behaviors HSDN C0026821 Cramp C0026850 Muscular dystrophy HSDN C0042963 Symptoms vomiting C0751908 Vestibular neuronitis HSDN C0003862 Pain joint C0007286 Carpal tunnel syndrome HSDN C0023015 Language handicap C4085311 Depression - recess HSDN C0242936 Center pain C0025299 Meningocele HSDN C1384666 Decreased hearing C0020541 Hypertension, portal HSDN C0042798 Vision dim C2350522 Touch perception HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019045 Hemoglobinopathies HSDN C1963071 Back pain adverse event C1881674 Medical device emits smoke HSDN C3829611 Nausea frequency C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0018784 Deafness sensorineural C0007787 Transient ischemic attack HSDN C2911647 Weight gain adverse event C1963106 Esophagitis adverse event HSDN C0013404 Respiratory difficulty C0007124 Noninfiltrating intraductal carcinoma HSDN C1963281 Vomiting adverse event C0021359 Infertility HSDN C3463815 Feel fatigue C0027708 Nephroblastoma HSDN C1963071 Back pain adverse event C0041948 Uremia HSDN C3641756 Have diarrhea C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0029882 Otitis media HSDN C0037316 Not enough sleeping C0015328 Behavior, exploratory HSDN C4084773 Bothered by weight gain C0001430 Adenoma HSDN C0018991 Paralysis one side of body C0039504 Injuries tendon HSDN C0030193 Sense of pain C0036346 Schizophrenia, childhood HSDN C0424755 Fever symptoms C1962971 Myocarditis adverse event HSDN C3539892 Pelvic pain in front C0007867 Cervix diseases HSDN C4084776 Weight loss C0026764 Multiple myeloma HSDN|HPO C0024032 Birth weight subnormal C2750805 Chromosome 5p13 duplication syndrome MalaCards C4085211 Pain distress question C3812171 Bradycardia by ecg finding HSDN C0002170 Alopecia disorders C0023795 Lipoid proteinosis of urbach and wiethe HPO C0036572 Convulsion C2931673 Ceroid lipofuscinosis, neuronal 1, infantile OrphaNet|HPO|MalaCards C0278152 Hemifacial spasms C0206716 Ganglioglioma HSDN C0151786 Weakness muscle C0023241 Legionnaires' disease MalaCards C2029884 Hearing loss by exam C0035801 Diseases rodent HSDN C0004134 Dyssynergia C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C0011570 Monopolar depression C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 HPO C1549543 Administration method - pain C0029944 Drug overdose HSDN C1962972 Proteinuria adverse event C3887532 Ulceration HSDN C1549543 Administration method - pain C0022578 Keratoconus HSDN C0206160 Retic count elevated C0002892 Anemia, pernicious HSDN C4085862 Bothered by nausea C0022890 Labyrinthine disorder HSDN C3274924 Have been coughing C0233629 Thinking and speaking disturbances HSDN C0023015 Language handicap C0026590 Child mother relationship HSDN C2984058 Have pain C0013922 Embolism HSDN C2237041 Shox gene with short stature C1428293 Slx4 gene HPO C2029884 Hearing loss by exam C0024437 Macular degeneration HSDN C0007398 Catatonic C0497327 Dementia HSDN C0026821 Cramp C0024117 Chronic obstructive airway disease HSDN C2242996 Tingling C0003850 Arteriosclerosis HSDN C0013390 Cramps menstrual C1548578 Location characteristic id - smoking HSDN C3244654 Sore throat brand of benzocaine & menthol C0043124 West nile fever MalaCards C4084773 Bothered by weight gain C0029443 Osteomyelitis HSDN C3539893 Pelvic pain occurs with intercourse C0017412 Genital diseases, male HSDN C0003467 Angst C0013384 Dyskinetic syndrome MalaCards C0042940 Disorder of voice C0036357 Psychology, schizophrenic HSDN C2911645 Weight loss adverse event C0852007 Scleroderma and associated disorders OrphaNet C0595939 Stillborn C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards|HPO C0031911 Pigment deposition C0004767 Bartholin cyst MalaCards C0042963 Symptoms vomiting C0003469 Anxiety disorders HSDN C2025995 Cellulitis C0013100 Dracontiasis OrphaNet|MalaCards C4084784 Diarrhea C0026847 Spinal muscular atrophy HSDN C2203646 Jaundice C0796561 Melanoma vaccines HSDN C4085317 Diarrhea frequency C0024899 Mastocytosis OrphaNet|MalaCards C3541349 Syncope C0042109 Urticaria HSDN C2203646 Jaundice C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C0577567 Mass of urogenital structure C1263786 Neoplasm of uterine adnexa UMLS C1963281 Vomiting adverse event C0001580 Adolescent behavior HSDN C0009080 Finger clubbing C0265295 Jansen type metaphyseal chondrodysplasia HPO C1882272 Pain adverse event by ctcae anatomic descriptor C1704212 Embolism embolus HSDN C0151786 Weakness muscle C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards C0026838 Spasticity muscle C4048196 Beta-mannosidosis HSDN C0522224 Palsied C0040997 Trigeminal neuralgia HSDN C2911645 Weight loss adverse event C0007137 Squamous cell carcinoma HSDN C0026205 Pupillary constriction C0014877 Esotropia HSDN C1963091 Diarrhea adverse event C0342859 Harderoporphyria HPO C4084802 Usual severity diarrhea C0039590 Testicular neoplasms HSDN C0030552 Paralysis partial C0027686 Pathologic neovascularization HSDN C0018777 Deafness, conductive C0236969 Substance-related disorders HSDN C1263846 Attention deficit disorder with hyperactivity C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C0853945 Oral mucosa blister C2673610 Jeb-i MalaCards|HPO C0030193 Sense of pain C0311312 External endometriosis UMLS C0018808 Murmur C0020517 Hypersensitivity HSDN C0018926 Emesis bloody C0040588 Tracheoesophageal fistula HSDN C4085211 Pain distress question C0016171 Fistula of intestine, excluding rectum and anus HSDN C2242996 Tingling C0027830 Neurofibroma HSDN C2984057 Have nausea C0000771 Abnormalities, drug induced HSDN C0031256 Petechia C3550789 Thrombocytopenia, x-linked, with or without dyserythropoietic anemia MalaCards C4085210 Usual severity pain C0004099 Asthma, exercise-induced HSDN C2237041 Shox gene with short stature C0265223 Cohen syndrome OrphaNet|HPO C2096293 Ent surgical result ear vertigo C0242287 Isaacs syndrome HPO C1961131 Cough adverse event C0238378 Desquamative interstitial pneumonia MalaCards C0018772 Deafness C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C0013604 Edematous C0948368 Kaufman-mckusick syndrome MalaCards|HPO C0014724 Burping C0034194 Pyloric stenosis HSDN C3887873 Hearing loss C0011875 Diabetic angiopathies HSDN C0036659 Sensation disorder C0038271 Stereotyped behavior HSDN C1963071 Back pain adverse event C0919267 Ovarian neoplasm HSDN C2024893 Cardiovascular surgery result: fatigue C0003869 Arthritis, infectious HSDN C1963093 Dizziness adverse event C2586211 Thrombosis of blood vessel HSDN C1963093 Dizziness adverse event C0033968 Psychotherapeutic technique HSDN C0018784 Deafness sensorineural C3551954 Coenzyme q10 deficiency, primary, 1 MalaCards C1963281 Vomiting adverse event C1306577 Dies patient HSDN C0036572 Convulsion C0004144 Atelectasis HSDN C0522224 Palsied C0020428 Hyperaldosteronism HSDN C1963071 Back pain adverse event C1334410 Localized primitive neuroectodermal tumor MalaCards C0043094 Weight gain C0020443 Hypercholesterolemia HSDN C4084724 Usual severity constipation C0041327 Tuberculosis, pulmonary HSDN C2029884 Hearing loss by exam C0038941 Incisional infection HSDN C0240211 Swelling lips C0600268 Cheilitis granulomatosa MalaCards C0030486 Extremity paralysis, lower C1963266 Uveitis adverse event HSDN C0028738 Nystagmus C3553788 Alternating hemiplegia of childhood 2 MalaCards C2237041 Shox gene with short stature C3150675 Chromosome 15q24 duplication syndrome HPO C1963091 Diarrhea adverse event C0030524 Paratuberculosis HSDN C0042928 Paralysis vocal cord C0752235 Lyme neuroborreliosis HSDN C0013395 Indigestion C1962986 Glaucoma adverse event HSDN C0003811 Cardiac rhythm disturbance C0751038 Cockayne syndrome, type ii HPO C0033377 Caudal displacement C1853120 Noonan syndrome 4 MalaCards|HPO C1963180 Neck pain adverse event C0206725 Subependymal glioma HSDN C1963137 Hydrocephalus adverse event C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome OrphaNet|HPO|MalaCards C0033774 Skin pruritus C0343101 Wells syndrome OrphaNet|MalaCards C0013604 Edematous C0022081 Iritis HSDN C4085862 Bothered by nausea C2937358 Cerebral hemorrhage HSDN C1963184 Nystagmus adverse event C3807567 Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome MalaCards C4085317 Diarrhea frequency C0268543 Hyperammonemia, type iii MalaCards C0013362 Dysarthrias C0751383 Juvenile neuronal ceroid lipofuscinosis MalaCards C3898969 Have been vomiting C0267830 Pyogenic liver abscess HSDN C3714772 Fever recurrent C3553937 Pbd4b MalaCards C0004134 Dyssynergia C0162635 Angelman syndrome OrphaNet|MalaCards C0035021 Fever, famine C0494042 Spirillosis MalaCards C1961131 Cough adverse event C0030305 Pancreatitis HSDN C0036572 Convulsion C0016542 Foreign body HSDN C0027796 Neuralgias C0003486 Aortic aneurysm HSDN C0018520 Breath odor C0038366 Stomatitis, herpetic HSDN C0013404 Respiratory difficulty C1956257 Pulmonary stenosis HSDN C3887638 Failure to thrive in infant C2931816 Chromosome 2, monosomy 2q24 OrphaNet|HPO|MalaCards C0231785 Spasm carpopedal C0039621 Tetany UMLS C0042571 Vertigo subjective C0521784 Otolith disease UMLS C0162298 Stiffness joints C0268543 Hyperammonemia, type iii MalaCards C0022638 Ketosis C2931660 Autosomal recessive fructose 1, 6-diphosphatase deficiency MalaCards C2203646 Jaundice C0014859 Esophageal neoplasms HSDN C0037384 Snore C0019693 Hiv infections HSDN C0019209 Large liver C1855109 Methylmalonic aciduria cbla type HPO C1856661 Cornea cloudy C0238286 Mucolipidosis type iv MalaCards|HPO C0011168 Disorder deglutition C0751603 Autosomal recessive hereditary spastic paraplegia MalaCards C4084769 Vomiting frequency C0035066 Renal artery obstruction HSDN C0018777 Deafness, conductive C1860145 Acrocraniofacial dysostosis OrphaNet|MalaCards C1963281 Vomiting adverse event C0016627 Avian influenza DiseaseOntology|MalaCards C0413252 Hypothermia due to exposure C0043049 Water intoxication HSDN C0027796 Neuralgias C0149521 Pancreatitis, chronic HSDN C0003469 Anxiety disorder C1857844 Williams-beuren region duplication syndrome OrphaNet|MalaCards C0019209 Large liver C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO C0019079 Bloody sputum C0020807 Pulmonary hemosiderosis idiopathic MalaCards|UMLS C1963071 Back pain adverse event C0595812 Fistula route HSDN C3463815 Feel fatigue C0018235 Aggrieved HSDN C3463815 Feel fatigue C0010346 Crohn disease HSDN C0036572 Convulsion C0220650 Metastatic malignant neoplasm to brain UMLS C0003910 Articulation disorder C0013386 Dyskinesia, drug-induced HSDN C4084784 Diarrhea C0024667 Animal mammary neoplasms HSDN C4085211 Pain distress question C0517960 Neurological status: consciousness HSDN C2203646 Jaundice C0856761 Budd-chiari syndrome MalaCards|HPO C3641755 Have constipation C0080179 Vertebra fracture HSDN C0241210 Speaking delay C3810001 Combined oxidative phosphorylation deficiency 18 MalaCards C0019572 Hairiness C1962979 Burn adverse event HSDN C2984058 Have pain C0013505 Cyst, pulmonary hydatid HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1414542 Fbn1 gene HSDN C0020458 Hyperhydrosis C1861848 Paragangliomas 4 MalaCards|HPO C0023012 Delay language C0038868 Progressive supranuclear palsy OrphaNet C0009421 Comatose C0220754 Biotinidase deficiency MalaCards|HPO C1069915 Vertigo C0022665 Kidney neoplasm HSDN C4085548 Usual severity dizziness C2713543 Biofeedback eeg HSDN C0036572 Convulsion C3495022 Atonic seizure, non-intractable UMLS C4084776 Weight loss C0236664 Alcohol-related disorders HSDN C0030554 Abnormal sensation C0034885 Rectal neoplasms HSDN C0042963 Symptoms vomiting C0022865 Obstetric labor complications HSDN C0241210 Speaking delay C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C0009792 Consciousness disorder C0595888 Phosphate serum decreased HSDN C0028738 Nystagmus C1860406 Vitreoretinochoroidopathy (disorder) MalaCards|HPO C0751495 Seizure focal C0009421 Comatose UMLS C3641755 Have constipation C1090821 Sepsis (invertebrate) HSDN C0016382 Cutaneous vascular engorgement C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C0851578 Disorder sleep C0018800 Cardiomegaly HSDN C0011991 Loose stools C0032227 Pleural effusion disorder HSDN C0878773 Bladder hyperactive C1548578 Location characteristic id - smoking HSDN C0042571 Vertigo subjective C3648280 Late effects of cerebral infarction vertigo UMLS C3463815 Feel fatigue C0032227 Pleural effusion disorder HSDN C0030975 Disorders perception C0700327 Clinical findings relating to memory HSDN C4085222 Nausea C1306577 Dies patient HSDN C0035078 Failure kidney C0162283 Nephrogenic diabetes insipidus HPO C1384666 Decreased hearing C0017636 Glioblastoma HSDN C4084726 Distress cough C0021361 Female infertility HSDN C1279888 Proteinuria of undiagnosed cause C0017185 Gastrointestinal neoplasms HSDN C0018989 Paresis of one side of body C0007787 Transient ischemic attack UMLS C0427190 Ataxia, truncal C0398746 Gluthathione synthetase deficiency MalaCards C0027066 Myoclonic jerking C0032285 Pneumonia HSDN C4085211 Pain distress question C0026691 Mucocutaneous lymph node syndrome HSDN C0009806 Constipate C0017658 Glomerulonephritis HSDN C0005874 Blush C1859316 Cataract-alopecia-sclerodactyly syndrome MalaCards C2242996 Tingling C0029456 Osteoporosis HSDN C0008031 Pain chest C0017589 Farcy DiseaseOntology|MalaCards C0042963 Symptoms vomiting C0032858 Powassan encephalitis MalaCards C0018784 Deafness sensorineural C0162834 Hyperpigmentation HSDN C1961131 Cough adverse event C0276108 Chlamydia infection psittaci HSDN C1549543 Administration method - pain C0009186 Coccidioidomycosis HSDN C0917816 Deficiency mental C1855787 Ichthyosis, mental retardation, dwarfism, and renal impairment MalaCards C0151825 Ostalgia C2698306 B acute lymphoblastic leukemia with t(1;19)(q23;p13.3); e2a-pbx1 (tcf3-pbx1) UMLS C0019209 Large liver C0268238 Triglyceride storage disease with ichthyosis MalaCards|HPO C4084723 Constipation C1384606 Dyspareunia HSDN C0028738 Nystagmus C4041558 Cone-rod synaptic disorder, congenital nonprogressive MalaCards C0015672 Decreased energy C1848030 Hypotonia-cystinuria syndrome OrphaNet|HPO|MalaCards C3539889 Pelvic pain increasing in severity C0017416 Genital neoplasms, female HSDN C0036572 Convulsion C0002170 Alopecia HSDN C0242936 Center pain C0398738 Leukocyte adhesion deficiency type 1 MalaCards C0028738 Nystagmus C1623209 Okihiro syndrome MalaCards C1959630 Eye pain adverse event C0302497 Retrobulbar haemorrhage HSDN C0040460 Dental pain C0003864 Arthritis HSDN C1963180 Neck pain adverse event C0037650 Somatoform disorder HSDN C0042571 Vertigo subjective C0700208 Acquired scoliosis HSDN C4084724 Usual severity constipation C1090821 Sepsis (invertebrate) HSDN C4084767 Bothered by vomiting C1299919 Enteric coccidiosis HSDN C2029884 Hearing loss by exam C0016063 Osteitis fibrosa disseminata HSDN C0000737 Abdomen pain C0027743 Nerve compression syndrome HSDN C0917816 Deficiency mental C1970827 Phosphoribosylpyrophosphate synthetase superactivity MalaCards|HPO C0003811 Cardiac rhythm disturbance C2931347 Cardiac form of generalized glycogenosis MalaCards C4084775 Usual severity weight loss C0038186 Reflex, startle HSDN C0038990 Sweats C1275074 Odonto-onycho-dermal dysplasia MalaCards C4084768 Usual severity vomiting C0020443 Hypercholesterolemia HSDN C1963091 Diarrhea adverse event C0004114 Astrocytoma HSDN C0013395 Indigestion C0032019 Pituitary neoplasms HSDN C0016199 Pain flank C0022661 Kidney failure, chronic UMLS C1963252 Tremor adverse event C3554605 Mc3dn2 MalaCards C0917816 Deficiency mental C0544862 Neurocutaneous melanosis OrphaNet C4085548 Usual severity dizziness C0034069 Pulmonary fibrosis HSDN C2984058 Have pain C0007684 Central nervous system infection HSDN C2237041 Shox gene with short stature C2678036 Craniofacioskeletal syndrome MalaCards C2911647 Weight gain adverse event C0027643 Neoplasm recurrence, local HSDN C1069915 Vertigo C0012644 Animal disease models HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0006262 Bronchial fistula HSDN C0011991 Loose stools C0700095 Central neuroblastoma MalaCards|HSDN C1384666 Decreased hearing C0243026 Sepsis HSDN C0042571 Vertigo subjective C0001580 Adolescent behavior HSDN C0022346 Yellow skin C0153458 Pancreas head cancer malignant MalaCards C1963091 Diarrhea adverse event C0003493 Aortic diseases HSDN C2911645 Weight loss adverse event C0030319 Panic disorder HSDN C2919142 Short stature adverse event C1303073 Nicolaides baraitser syndrome MalaCards|HPO C0233514 Behavior abnormal C0796085 Nance-horan syndrome MalaCards|HPO C4085317 Diarrhea frequency C0038160 Staphylococcal infections HSDN C1961131 Cough adverse event C1540912 Hypereosinophilic syndrome HSDN C4084774 Have weight loss C0009651 Conditioning operant HSDN C1549543 Administration method - pain C0085395 Ureaplasma infections HSDN C4084768 Usual severity vomiting C0175683 Citrullinemia HPO C3665492 Pigmentations C0334233 Pleomorphic carcinoma MalaCards C4084725 Usual severity cough C0037120 Pneumonia, nitrogen dioxide HSDN C0349588 Stature short C2675875 Chromosome 2p16.1 p15 deletion syndrome MalaCards C0009398 Color vision defects C0314719 Dryness of eye HSDN C0019209 Large liver C0241954 Jaundice, infectious MalaCards C0018681 Headache, cephalalgia C1332200 Adult diffuse astrocytoma UMLS C0013604 Edematous C0028796 Dermatitis, occupational HSDN C0004134 Dyssynergia C0015458 Facial hemiatrophy MalaCards|UMLS C3463815 Feel fatigue C0017612 Glaucoma, open-angle HSDN C0030552 Paralysis partial C0001973 Alcoholic intoxication, chronic HSDN C4085317 Diarrhea frequency C0027794 Neural tube defects HSDN C0030193 Sense of pain C0025281 Meniere disease HSDN C0036572 Convulsion C3494929 Juvenile absence epilepsy, intractable UMLS C0035232 Diaphragmatic paralysis C0041327 Tuberculosis, pulmonary HSDN C0242936 Center pain C0013502 Echinococcosis HSDN C0009806 Constipate C0205788 Histiocytoid hemangioma HSDN C3146279 Coma C4049644 Depression HSDN C0086437 Joint hypermobility C3280616 Cranioectodermal dysplasia 4 MalaCards C0012833 Dizzy C0014474 Ependymoma HSDN C0027066 Myoclonic jerking C0024299 Lymphoma HSDN C2315100 Pediatric failure to thrive C0795851 14 trisomy mosaicism syndrome OrphaNet|MalaCards C0151686 Growth retardation C0432337 Cutis laxa, recessive, type ii OrphaNet C0424755 Fever symptoms C0206743 Rhabdoid tumor OrphaNet|MalaCards C4085211 Pain distress question C0162869 Aneurysm, ruptured HSDN C3539023 Pelvic pain increasing in frequency C0001442 Adenosarcoma HSDN C0027497 Queasy C0085111 Ankle injury HSDN C0018772 Deafness C0012691 Dislocations HSDN C0027497 Queasy C0270858 Abdominal migraines MalaCards C0162298 Stiffness joints C2931515 Piussan lenaerts mathieu syndrome OrphaNet|MalaCards C1384666 Decreased hearing C1853102 Cerebrooculofacioskeletal syndrome 2 MalaCards|HPO C0013604 Edematous C0030499 Parasitic diseases HSDN C4084766 Vomiting C0268573 Valinemia MalaCards C0026838 Spasticity muscle C2751318 Nijmegen breakage syndrome-like disorder MalaCards|HPO C4084766 Vomiting C0021432 Infratentorial neoplasms HSDN C0035078 Failure kidney C2717836 Steroid sulfatase deficiency disease MalaCards C0011991 Loose stools C0023176 Lead poisoning MalaCards|HSDN C0460137 Push down or depress C0268250 Gaucher disease, type 2 (disorder) MalaCards C3641755 Have constipation C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C1963064 Anxiety adverse event C0001529 Dercum disease OrphaNet|MalaCards C1963091 Diarrhea adverse event C0016397 Focal infection HSDN C2029884 Hearing loss by exam C0314657 Genetic predisposition HSDN C0018965 Blood urine C0206743 Rhabdoid tumor OrphaNet|MalaCards C0020673 Hypothermia (central) (local) C0027746 Nerve degeneration HSDN C0031911 Pigment deposition C3540845 Microphthalmia, isolated, with coloboma 8 MalaCards C0037763 Spasm C1579931 Depressed - symptom HSDN C0040264 Ear ringing sound C0014544 Epilepsy HSDN C4084727 Cough frequency C0027831 Neurofibromatosis 1 HSDN C0878773 Bladder hyperactive C0013363 Dysautonomia HSDN C0232726 Tenesmus, rectal C2981237 Stage iv rectosigmoid cancer ajcc v6 UMLS C0011991 Loose stools C0019348 Herpes simplex infections HSDN C2024893 Cardiovascular surgery result: fatigue C0740277 Bile duct carcinoma OrphaNet|HPO C0002170 Alopecia disorders C0043346 Xeroderma pigmentosum MalaCards|HPO C4085210 Usual severity pain C0236733 Amphetamine-related disorders HSDN C2048468 Inability to impregnate C1857395 De toni-debre-fanconi syndrome HPO C0497406 Over weight C3495422 Finding relating to sexuality and sexual activity HSDN C0000737 Abdomen pain C0013299 Duodenogastric reflux HSDN C0042963 Symptoms vomiting C0333355 Inflammatory disease of mucous membrane HSDN C4084784 Diarrhea C0018800 Cardiomegaly HSDN C0581358 Gastric spasm C0038354 Stomach diseases UMLS C0242670 Chronic vegetative state C0497327 Dementia HSDN C0026821 Cramp C0032238 Bornholm disease HSDN C0018772 Deafness C3266101 22q11 partial monosomy syndrome OrphaNet C1549543 Administration method - pain C0007760 Cerebellar diseases HSDN C0030193 Sense of pain C0031149 Peritoneal neoplasms HSDN C0015469 Facial paralysis C0751941 Glossopharyngeal nerve disease or syndrome HSDN C2984058 Have pain C0013238 Dry eye syndromes HSDN C2984058 Have pain C2117329 X-ray of toe: polydactyly HSDN C0012569 Double vision C0011849 Diabetes mellitus HSDN C0034124 Pupillary disorder C0752294 Sleep arousal disorders HSDN C0018991 Paralysis one side of body C0525045 Mood disorders HSDN C4084767 Bothered by vomiting C0001580 Adolescent behavior HSDN C0018965 Blood urine C0023374 Lesch-nyhan syndrome OrphaNet|HPO|MalaCards C4084766 Vomiting C0339959 Pneumonia chlamydial HSDN C0575081 Abnormal gait C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia HPO C0027498 Nausea vomiting C1833511 Carnitine palmitoyltransferase ii deficiency, infantile OrphaNet|HPO C0018772 Deafness C3888013 Hypnoses HSDN C0015672 Decreased energy C0008313 Cholangitis, sclerosing HSDN C0015938 Fetal macrosomia C0014544 Epilepsy HSDN C4084725 Usual severity cough C0032290 Aspiration pneumonia MalaCards C1963184 Nystagmus adverse event C1836395 Spinocerebellar ataxia 26 HPO C0232466 Feeding difficulty C3502298 Lactic acidosis, fatal infantile MalaCards C0018991 Paralysis one side of body C0038160 Staphylococcal infections HSDN C2129203 Abdominal pain initiated or exacerbated by taking medication C0341201 Drug-induced gi disturbance UMLS C3815497 Cough C0004576 Babesiosis OrphaNet|MalaCards C0241210 Speaking delay C0024408 Machado-joseph disease OrphaNet|MalaCards C0018965 Blood urine C2931360 Weber klippel trenaunay MalaCards C0013608 Cardiac edema C0282492 Sneddon syndrome HSDN C0086437 Joint hypermobility C0796004 Kabuki make-up syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C0042963 Symptoms vomiting C0341106 Eosinophilic esophagitis MalaCards|HSDN|UMLS C0024312 Lymphocytopenia C2931242 Familial waldmann's disease MalaCards C1279888 Proteinuria of undiagnosed cause C0029456 Osteoporosis HSDN C0518090 Frequency of pain question C0520459 Necrotizing enterocolitis HSDN C0027066 Myoclonic jerking C1998254 Myoclonus of tensor tympani muscle UMLS C4084726 Distress cough C0153416 Malig neop oth spec part oesop MalaCards C1549543 Administration method - pain C0752235 Lyme neuroborreliosis HSDN C4084775 Usual severity weight loss C0038579 Substance abuse, intravenous HSDN C0036572 Convulsion C1855861 Glycogen storage disease 0, liver MalaCards|HPO C0041105 Jaw spasm C0043352 Xerostomia HSDN C2315100 Pediatric failure to thrive C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0424755 Fever symptoms C0038271 Stereotyped behavior HSDN C0003811 Cardiac rhythm disturbance C0039235 Tachycardia, ectopic junctional OrphaNet|MalaCards C0036572 Convulsion C0344488 Absence; cerebellum OrphaNet C0009792 Consciousness disorder C0149931 Migraine disorders HSDN C1384666 Decreased hearing C2931291 Familial spastic paraparesis and deafness MalaCards C4084784 Diarrhea C0042133 Uterine fibroids HSDN C1963184 Nystagmus adverse event C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C0023012 Delay language C1845366 Mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance MalaCards|HPO C0036572 Convulsion C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0041834 Erythematous condition C0343055 Generalized pustular psoriasis MalaCards C2911645 Weight loss adverse event C0036357 Psychology, schizophrenic HSDN C0013362 Dysarthrias C0878675 Erdheim-chester disease MalaCards C2203646 Jaundice C0023518 Leukocytosis HSDN C0004604 Pain back C0750242 Vertebra scoliosis UMLS C0004134 Dyssynergia C0085220 Cerebral amyloid angiopathy HSDN C4084766 Vomiting C0000833 Abscess HSDN C4084774 Have weight loss C0017658 Glomerulonephritis HSDN C0018772 Deafness C0007766 Intracranial aneurysm HSDN C0042798 Vision dim C0035304 Retinal degeneration HSDN C3641755 Have constipation C0037997 Splenic diseases HSDN C1963170 Hypothermia adverse event C4085311 Depression - recess HSDN C0013421 Dystonia C1970269 Choreoathetosis, hypothyroidism, and neonatal respiratory distress HPO C4085317 Diarrhea frequency C0239981 Hypoalbuminemia HSDN C2242996 Tingling C0019069 Hemophilia a HSDN C0349588 Stature short C0795818 Chromosome 7 ring syndrome OrphaNet|MalaCards C0231528 Muscle pain generalized C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0003550 Broca aphasia C0033906 Psychological theories HSDN C0013404 Respiratory difficulty C0034929 Reflex HSDN C1963281 Vomiting adverse event C1552262 Nurse practitioner - family HSDN C0027498 Nausea vomiting C0033822 Pseudomyxoma peritonei MalaCards C1557397 Adverse event associated with pain C0034063 Pulmonary edema HSDN C4084768 Usual severity vomiting C2984572 Malaria pathway HSDN C0042755 Virilisation C0011570 Mental depression HSDN C0042963 Symptoms vomiting C0022660 Kidney failure, acute UMLS C0016927 Gag reflex C0037313 Sleep HSDN C4084766 Vomiting C0003950 Ascariasis HSDN C0042571 Vertigo subjective C1866039 Episodic ataxia, type 5 MalaCards C0035229 Respiratory function impaired C1306794 Wound botulism MalaCards C0349506 Sun sensitivity C1833561 Uv-sensitive syndrome HPO C0030552 Paralysis partial C0042170 Uveomeningoencephalitic syndrome HSDN C0518090 Frequency of pain question C0085082 Fungemia HSDN C3641756 Have diarrhea C0456889 Enteropathy-associated t-cell lymphoma HSDN C0012569 Double vision C0033975 Psychotic disorders HSDN C0700078 Deep tendon reflex decrease C1847903 Charcot-marie-tooth neuropathy, dominant intermediate b, with neutropenia HPO C0030193 Sense of pain C1335367 Parotid gland squamous cell carcinoma UMLS C0018784 Deafness sensorineural C0039590 Testicular neoplasms HSDN C4085642 Level of joint stiffness C3683846 Chromosome 17p deletion syndrome MalaCards C0030486 Extremity paralysis, lower C0026598 Movement perception HSDN C0009806 Constipate C0007789 Cerebral palsy HSDN C3539023 Pelvic pain increasing in frequency C0002989 Epithelioid hemangioma of skin HSDN C0036396 Sciatica C0004364 Autoimmune diseases HSDN C2984058 Have pain C0013117 Dreaming HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014571 Epiphyses, slipped HSDN C2237041 Shox gene with short stature C1850040 Pelviscapular dysplasia OrphaNet|HPO|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0018099 Gout HSDN C0027497 Queasy C3812171 Bradycardia by ecg finding HSDN C0042571 Vertigo subjective C1960869 Vertigo as late effect of stroke UMLS C0452143 Flaccid paraplegia C0030486 Paraplegia UMLS C2919142 Short stature adverse event C1852576 Copper deficiency, familial benign OrphaNet|MalaCards C4085222 Nausea C0013922 Embolism HSDN C4084769 Vomiting frequency C0040411 Tongue neoplasms HSDN C1963281 Vomiting adverse event C0011581 Depressive disorder HSDN C1963067 Atrial fibrillation adverse event C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) HPO C0152169 Colic renal C0034359 Cell pus urine HSDN C4084784 Diarrhea C1859407 Bone dysplasia, lethal, holmgren type MalaCards C0917816 Deficiency mental C0265248 Ruvalcaba syndrome OrphaNet|MalaCards C3541349 Syncope C0021361 Female infertility HSDN C2237041 Shox gene with short stature C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C0013528 Echo speech C0004377 Automatism HSDN C0026838 Spasticity muscle C1848410 Xeroderma pigmentosum, variant type MalaCards C0013404 Respiratory difficulty C0242216 Biliary calculi HSDN C0042571 Vertigo subjective C0036357 Psychology, schizophrenic HSDN C0011168 Disorder deglutition C1834339 Myopathy, actin, congenital, with excess of thin myofilaments HPO C0011991 Loose stools C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C3665347 Vision impaired C1510455 Acrocephalosyndactylia MalaCards|HPO C0003469 Anxiety disorder C2675369 Chromosome 22q11.2 microduplication syndrome HPO C2024893 Cardiovascular surgery result: fatigue C0155866 Inhalational anthrax OrphaNet|MalaCards C1963091 Diarrhea adverse event C0038644 Sudden infant death syndrome HSDN C0027497 Queasy C0040479 Torsades de pointes HSDN C0271215 Blindness legal C2677299 Cerebroretinal microangiopathy with calcifications and cysts (disorder) HPO C0010520 Skin cyanosis C0038454 Cerebrovascular accident HSDN C2984058 Have pain C0007130 Mucinous adenocarcinoma HSDN C4084775 Usual severity weight loss C0007453 Cattle disease HSDN C3887638 Failure to thrive in infant C2931187 Nephropathic cystinosis MalaCards C2984058 Have pain C0035436 Rheumatic fever HSDN C0033377 Caudal displacement C0796092 Oculo-cerebro-cutaneous syndrome OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0032249 Plummer vinson syndrome HSDN C0027498 Nausea vomiting C0018553 Hamartoma syndrome, multiple MalaCards C0497247 Blood pressure elevation C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084776 Weight loss C0014858 Esophageal motility disorders HSDN C0027497 Queasy C0011854 Diabetes mellitus, insulin-dependent HSDN C0023530 Leukopenia C3697183 Irak-4 - interleukin-1 receptor-associated kinase 4 deficiency MalaCards C0036659 Sensation disorder C0027902 Neuropsychological diagnosis HSDN C4085661 Usual severity nausea C0018799 Heart diseases HSDN C0019079 Bloody sputum C1336137 Stage ib adenocarcinoma of lung UMLS C4084768 Usual severity vomiting C0037036 Sialorrhea HSDN C2169806 Tic C0039082 Syndrome HSDN C0039070 Collapse fleeting C0007384 Cataplexy HSDN C0162298 Stiffness joints C2931162 Blepharophimosis radioulnar synostosis OrphaNet|MalaCards C2911647 Weight gain adverse event C1704272 Benign prostatic hyperplasia HSDN C0233514 Behavior abnormal C1829703 Carnitine palmitoyl transferase 1a deficiency OrphaNet|HPO C3641755 Have constipation C0334533 Arteriovenous hemangioma HSDN C0003862 Pain joint C0032285 Pneumonia HSDN C0424755 Fever symptoms C2028283 History of premature birth HSDN C1963091 Diarrhea adverse event C0037355 Smallpox vaccines HSDN C4085317 Diarrhea frequency C0032064 Plague HSDN C4084774 Have weight loss C0032344 Poisoning aspects HSDN C0039070 Collapse fleeting C0035828 Romano-ward syndrome MalaCards|HPO|UMLS C0011206 Delirium acute C2137063 Ent surgical result - speech HSDN C4084768 Usual severity vomiting C0033586 Failure, prosthesis HSDN C0036572 Convulsion C0001580 Adolescent behavior HSDN C4085210 Usual severity pain C0027439 Nasopharyngeal neoplasms HSDN C4084768 Usual severity vomiting C0013336 Dwarfism HSDN C2919142 Short stature adverse event C1842082 Vater-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency OrphaNet|MalaCards C0242936 Center pain C0040436 Dental erosion HSDN C4084773 Bothered by weight gain C1555914 Psychologist - psychotherapy, group HSDN C4084769 Vomiting frequency C0242350 Erectile dysfunction HSDN C0151786 Weakness muscle C0040411 Tongue neoplasms HSDN C4084773 Bothered by weight gain C0376550 Astroviridae infection HSDN C0040822 D tremors C2931426 Orofaciodigital syndrome type1 HPO C0030552 Paralysis partial C1865290 Hyperinsulinemic hypoglycemia, familial, 3 MalaCards C0576456 Poor feeding C0520681 Central alveolar hypoventilation syndrome MalaCards C4085862 Bothered by nausea C3150933 Hyperaldosteronism, familial, type iii MalaCards C0349588 Stature short C2678480 Chromosome 22q11.2 deletion syndrome, distal OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0268328 Porphobilinogen synthase deficiency MalaCards C4084773 Bothered by weight gain C0036982 Shock, hemorrhagic HSDN C0015672 Decreased energy C0026691 Mucocutaneous lymph node syndrome OrphaNet|MalaCards C4085317 Diarrhea frequency C0015456 Facial dermatoses HSDN C0031315 Phantom limb pain C0009088 Cluster headache HSDN C0600142 Flash hot C0042133 Uterine fibroids HSDN C4085210 Usual severity pain C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C1579931 Depressed - symptom C1856493 Gaucher disease, norrbottnian type HPO C4049644 Depression C0795907 Conotruncal anomaly face syndrome MalaCards C0020455 Hypergammaglobulinemia C0020758 Congenital ichthyosis HSDN C3539891 Pelvic pain to the rear C0042996 Vulvitis unspecified HSDN C3539896 Pelvic pain occurs with urination C0205788 Histiocytoid hemangioma HSDN C1963063 Anorexia adverse event C0019829 Hodgkin disease OrphaNet C0242936 Center pain C0008928 Cleidocranial dysplasia HSDN C4085317 Diarrhea frequency C0011854 Diabetes mellitus, insulin-dependent HSDN C4084784 Diarrhea C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0234146 Absent reflex C1842983 Charcot-marie-tooth disease, axonal, type 2k MalaCards|HPO C4084784 Diarrhea C0600564 Self-efficacy HSDN C1963252 Tremor adverse event C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0015230 Exanthem C0023646 Lichen planus UMLS C0012569 Double vision C0338078 Non-functioning pituitary gland neoplasm MalaCards C3641756 Have diarrhea C0016663 Pathological fracture HSDN C2184232 Left arm soft tissue swelling C0037580 Soft tissue swelling UMLS C0012569 Double vision C0007760 Cerebellar diseases HSDN C0003467 Angst C2676739 Chromosome 2q32-q33 deletion syndrome MalaCards|HPO C4085549 Dizziness C0027658 Neoplasms, germ cell and embryonal HSDN C1999266 Depression adverse event C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C1963087 Constipation adverse event C0013080 Down syndrome HSDN C4085211 Pain distress question C0265706 Gastroschisis HSDN C0018772 Deafness C0002726 Amyloidosis HSDN C0013395 Indigestion C0919267 Ovarian neoplasm HSDN C0518090 Frequency of pain question C0023443 Hairy cell leukemia HSDN C0042571 Vertigo subjective C0270611 Brain damage HSDN C0013604 Edematous C0004153 Atherosclerosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0004114 Astrocytoma HSDN C0424755 Fever symptoms C3887662 Intraspinal neoplasm HSDN C0009806 Constipate C0024228 Lymphatic diseases HSDN C0036572 Convulsion C0520679 Sleep apnea, obstructive HSDN C3539023 Pelvic pain increasing in frequency C0206630 Endometrial stromal sarcoma HSDN C4084784 Diarrhea C0042018 Urinary calculi HSDN C3887638 Failure to thrive in infant C3151209 Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome HPO C0022107 Fussiness C0265321 Wyburn-mason syndrome MalaCards C3641755 Have constipation C0014544 Epilepsy HSDN C0028961 Urine output decreased C0038819 Siriasis HSDN C0027066 Myoclonic jerking C0019196 Hepatitis c HSDN C0009676 Confusion state C1962986 Glaucoma adverse event HSDN C4084767 Bothered by vomiting C1563705 Nephrogenic diabetes insipidus, type i HPO C0027796 Neuralgias C0158266 Intervertebral disc degeneration HSDN C0027498 Nausea vomiting C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0013404 Respiratory difficulty C0035243 Respiratory tract infections HSDN C0026884 Muteness C0015618 Families therapy HSDN C4085317 Diarrhea frequency C0242550 Behavior, risk reduction HSDN C4084768 Usual severity vomiting C0014869 Peptic esophagitis HSDN C2024893 Cardiovascular surgery result: fatigue C0003486 Aortic aneurysm HSDN C0241137 Skin pallor C0032749 Post-kala-azar dermal leishmaniasis MalaCards C0520909 Ponv C0007097 Carcinomas HSDN C0012833 Dizzy C0155496 Active meniere's-cochleovestib UMLS C4084774 Have weight loss C0003496 Aortic rupture HSDN C1549543 Administration method - pain C0302280 Adrenogenital syndrome HSDN C0009676 Confusion state C2932716 Pseudohypoparathyroidism type 1c HPO C0013608 Cardiac edema C0553980 Endomyocardial fibrosis HSDN C1963065 Apnea adverse event C1552527 Clinic / center - developmental disabilities HSDN C0242936 Center pain C0005604 Trauma birth HSDN C0030552 Paralysis partial C0553586 Cafe-au-lait macules with pulmonary stenosis MalaCards C0036572 Convulsion C0021832 Intestinal diseases, parasitic HSDN C4084727 Cough frequency C0019693 Hiv infections HSDN C0042025 Urinary incontinence stress C0227791 Discharge vaginal HSDN C0878773 Bladder hyperactive C0011581 Depressive disorder HSDN C0040264 Ear ringing sound C2713543 Biofeedback eeg HSDN C0026838 Spasticity muscle C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HSDN|UMLS|HPO|MalaCards C0011991 Loose stools C0267436 Noninfectious diarrhea, nos UMLS C0184567 Pain acute C0042338 Herpesvirus 3, human HSDN C0518090 Frequency of pain question C0037072 Diseases sigmoid HSDN C0041834 Erythematous condition C0162569 Hepatoerythropoietic porphyria MalaCards C4085211 Pain distress question C1414542 Fbn1 gene HSDN C0019209 Large liver C1842704 Gaucher disease, perinatal lethal OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0175683 Citrullinemia HPO C2237041 Shox gene with short stature C1845168 Hypophosphatemic rickets, x-linked recessive MalaCards|HPO C0013428 Painful urination C0855178 Stage iii bladder adenocarcinoma UMLS C3829611 Nausea frequency C0152164 Cyclical vomiting syndrome (disorder) MalaCards C0018784 Deafness sensorineural C0017612 Glaucoma, open-angle HSDN C0917816 Deficiency mental C3887608 Hydrocephalus, nonsyndromic, autosomal recessive 1 MalaCards C4020887 Photodysphoria C1970236 Microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen MalaCards|HPO C1557397 Adverse event associated with pain C0025517 Metabolic diseases HSDN C1963184 Nystagmus adverse event C0265308 Baller-gerold syndrome MalaCards|HPO C0042963 Symptoms vomiting C0007131 Non-small cell lung carcinoma HSDN C4085210 Usual severity pain C0001828 Agricultural workers' diseases HSDN C4085661 Usual severity nausea C0035066 Renal artery obstruction HSDN C0018991 Paralysis one side of body C2931746 Sulfocysteinuria HPO C0036572 Convulsion C2936830 Chromosome 13 duplication OrphaNet|MalaCards C1963071 Back pain adverse event C0153460 Malignant neoplasm of tail of pancreas MalaCards C3898969 Have been vomiting C0339959 Pneumonia chlamydial HSDN C0000737 Abdomen pain C2937421 Prostatic hyperplasia HSDN C4049644 Depression C0032533 Polymyalgia rheumatica MalaCards C0033774 Skin pruritus C0030846 Penile diseases HSDN C2237041 Shox gene with short stature C1961835 Gaucher disease, type 1 MalaCards C1963091 Diarrhea adverse event C0524620 Metabolic syndrome x HSDN C4084776 Weight loss C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0029396 Heterotopic ossification HSDN C0518090 Frequency of pain question C0265706 Gastroschisis HSDN C4084775 Usual severity weight loss C0013595 Eczema HSDN C4084766 Vomiting C0018805 Heart injuries HSDN C0004941 Behavioral symptoms C0205898 Pineoblastoma OrphaNet|MalaCards C0030552 Paralysis partial C2945560 Hemolytic HSDN C0042963 Symptoms vomiting C0025290 Aseptic meningitis HSDN C2024878 Cardiovascular surgery result: dyspnea C1306794 Wound botulism OrphaNet|MalaCards C0030552 Paralysis partial C1968741 Gsd iiic HPO C0039070 Collapse fleeting C1720983 Channelopathies HSDN C0020580 Decreased sensation C0003864 Arthritis HSDN C0028738 Nystagmus C0265428 9p+ syndrome MalaCards C0009421 Comatose C0010276 Craniopharyngioma MalaCards|HPO C0026858 Musculoskeletal pain C1963233 Seroma adverse event HSDN C4084726 Distress cough C0339946 Pulmonary tularemia DiseaseOntology|MalaCards C0004604 Pain back C0030920 Peptic ulcer HSDN C0008031 Pain chest C0027663 Neoplasms, multiple primary HSDN C0039070 Collapse fleeting C0001973 Alcoholic intoxication, chronic HSDN|UMLS C3815497 Cough C3244301 Coverage level - family HSDN C0019521 Hiccoughs C0870956 Neuropsychiatry HSDN C1549543 Administration method - pain C0001427 Adenoiditis, nos MalaCards C0018681 Headache, cephalalgia C3897751 Recurrent childhood gliomatosis cerebri UMLS C4084769 Vomiting frequency C0000833 Abscess HSDN C0013404 Respiratory difficulty C0282548 Leukostasis HSDN C0030193 Sense of pain C1555865 Forensic psychiatry HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1266101 Thymic epithelial tumor OrphaNet C2096293 Ent surgical result ear vertigo C2609414 Acute kidney injury HSDN C0040822 D tremors C0085096 Peripheral vascular diseases HSDN C0019825 Voice hoarseness C1334597 Malignant germ cell neoplasm of mediastinum UMLS C0011991 Loose stools C0014761 Erythroblastosis, fetal HSDN C1963087 Constipation adverse event C1970431 Pitt-hopkins syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0009241 Cognition disorders HSDN C0009676 Confusion state C0020635 Hypopituitarism HSDN C0009421 Comatose C0276379 La crosse encephalitis MalaCards C0015672 Decreased energy C0019097 Hemorrhagic fever, argentinian MalaCards C0020580 Decreased sensation C0003467 Anxiety HSDN C0085631 Abnormal excitement C0017601 Glaucomas HSDN C0344428 Ventricular tachycardia by ecg finding C1834481 Cardiomyopathy, dilated, 1s MalaCards C0020578 Hyperventilate C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0042384 Vasculitis, nonspecific C0043194 Wiskott-aldrich syndrome MalaCards|HPO C0917816 Deficiency mental C2931817 Chromosome 2q37 deletion syndrome OrphaNet|HPO|MalaCards C3539892 Pelvic pain in front C0302148 Blood clot HSDN C0023885 Liver abscess C2239176 Liver carcinoma MalaCards C0221263 Cafe au lait spot C0004114 Astrocytoma HSDN C1549543 Administration method - pain C0243010 Viral encephalitis HSDN C0028961 Urine output decreased C0003486 Aortic aneurysm HSDN C0039070 Collapse fleeting C0967777 Mok protein, human HSDN C0024031 Back pain lower back C1090821 Sepsis (invertebrate) HSDN C4085862 Bothered by nausea C0007222 Cardiovascular diseases HSDN C0000737 Abdomen pain C3899976 Bclc stage d adult hepatocellular carcinoma UMLS C0020580 Decreased sensation C0085119 Foot ulcer HSDN C0015469 Facial paralysis C1865143 Branchiootic syndrome 1 MalaCards C3887873 Hearing loss C0027765 Nervous system disorder HSDN C4085211 Pain distress question C0007774 Cerebral arterial diseases HSDN C0009676 Confusion state C0001418 Adenocarcinoma HSDN C0557874 Global developmental delay C2675859 Diamond-blackfan anemia 5 MalaCards|HPO C4084768 Usual severity vomiting C0852654 21-hydroxylase deficiency MalaCards C0020450 Hyperemesis gravidarum C0021294 Infant, premature UMLS C0241210 Speaking delay C0241932 X-linked hypogammaglobulinemia HPO C4049602 Hyperactivity C1857855 Spastic paraplegia 29, autosomal dominant MalaCards C0042928 Paralysis vocal cord C0344315 Depressed mood HSDN C4085549 Dizziness C0022661 Kidney failure, chronic HSDN C1963090 Dehydration adverse event C0079154 Congenital nonbullous ichthyosiform erythroderma MalaCards C4084724 Usual severity constipation C0020676 Hypothyroidism HSDN C0231528 Muscle pain generalized C0151436 Vasculitis, leukocytoclastic, cutaneous OrphaNet|MalaCards C4085210 Usual severity pain C0399352 Developmental absence of tooth HSDN C0011991 Loose stools C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C1963086 Confusion adverse event C1963067 Atrial fibrillation adverse event HSDN C0344315 Mood depressed C1568248 Usher syndrome, type iii MalaCards|HPO C0233407 Disorient C0014057 Japanese encephalitis DiseaseOntology|MalaCards C0018784 Deafness sensorineural C3150658 Warsaw breakage syndrome MalaCards C4085862 Bothered by nausea C0033893 Tension headache HSDN C0151786 Weakness muscle C1856302 Gsd iv, nonprogressive hepatic HPO C0030552 Paralysis partial C1846170 Mental retardation, x-linked, syndromic 7 OrphaNet|MalaCards C0424755 Fever symptoms C0042214 Vaccinia MalaCards C4084784 Diarrhea C1832322 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive HPO C2919142 Short stature adverse event C2931506 Stern lubinsky durrie syndrome MalaCards C0036572 Convulsion C3150909 D-2-hydroxyglutaric aciduria 2 MalaCards|HPO C0018772 Deafness C0014866 Esophageal stenosis HSDN C0000731 Abdomen distention C2940786 Thyroid hormone resistance syndrome HPO C1963281 Vomiting adverse event C1555914 Psychologist - psychotherapy, group HSDN C0086439 Activity decreased C1419149 Pex2 gene HSDN C0018784 Deafness sensorineural C1853223 Deafness, autosomal recessive 67 MalaCards|HPO C3898969 Have been vomiting C0796561 Melanoma vaccines HSDN C1549543 Administration method - pain C0023220 Leg injury HSDN C4084766 Vomiting C0021051 Immunologic deficiency syndromes HSDN C4084723 Constipation C0008924 Cleft lip HSDN C1963087 Constipation adverse event C0023895 Liver diseases HSDN C2315100 Pediatric failure to thrive C0268547 Argininosuccinic aciduria MalaCards|HPO C1549543 Administration method - pain C0034012 Delayed puberty HSDN C3641756 Have diarrhea C0010606 Adenoid cystic carcinoma HSDN C0151686 Growth retardation C1970431 Pitt-hopkins syndrome MalaCards C0030552 Paralysis partial C2931642 Benign symmetrical lipomatosis HSDN C4084725 Usual severity cough C0024899 Mastocytosis MalaCards C0030486 Extremity paralysis, lower C0020456 Hyperglycemia HSDN C0030486 Extremity paralysis, lower C0016663 Pathological fracture HSDN C0917816 Deficiency mental C0268125 Purine-nucleoside phosphorylase deficiency HPO C0151740 Intracranial hypertension C0205898 Pineoblastoma OrphaNet|MalaCards C0009421 Comatose C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0008031 Pain chest C0033860 Psoriasis HSDN C0042928 Paralysis vocal cord C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C1549543 Administration method - pain C0040436 Dental erosion HSDN C4084784 Diarrhea C0040336 Tobacco use disorder HSDN C4084774 Have weight loss C0025063 Mediastinal neoplasms HSDN C2203646 Jaundice C0346647 Malignant neoplasm of pancreas MalaCards C0878773 Bladder hyperactive C1881674 Medical device emits smoke HSDN C3887873 Hearing loss C1851878 Orofacial cleft 8 MalaCards C1963180 Neck pain adverse event C0039144 Syringomyelia HSDN C0036572 Convulsion C0079744 Diffuse large b-cell lymphoma HSDN C0033377 Caudal displacement C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C2127293 Fainting preceded by seeing an animal C0340849 Fainting simple UMLS C1860844 Sparse, thin hair C0265449 Pallister-killian syndrome OrphaNet|MalaCards C2984058 Have pain C0042018 Urinary calculi HSDN C3539893 Pelvic pain occurs with intercourse C0010068 Coronary heart disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0024031 Back pain lower back C0848377 Trauma to the abdomen HSDN C4085862 Bothered by nausea C0717360 Disease lyme vaccine HSDN C0242936 Center pain C0023487 Acute promyelocytic leukemia HSDN C0042024 Urine incontinence C3463824 Myelodysplastic syndrome HSDN C3887638 Failure to thrive in infant C1859407 Bone dysplasia, lethal, holmgren type MalaCards C1963170 Hypothermia adverse event C0011881 Diabetic nephropathy HSDN C0015970 Fever unknown origin C1253943 Fluid in the chest HSDN C3539023 Pelvic pain increasing in frequency C0020550 Hyperthyroidism HSDN C4084774 Have weight loss C0027659 Neoplasms, experimental HSDN C0013362 Dysarthrias C0206734 Hemangioblastoma HSDN C0518090 Frequency of pain question C0012813 Diverticulitis HSDN C3463815 Feel fatigue C0019061 Hemolytic-uremic syndrome HSDN C0041667 Low weight C0268242 Niemann-pick disease, type a MalaCards C0277799 Fever intermittent C0398691 Hyperimmunoglobulinemia d OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0272203 Indolent systemic mastocytosis OrphaNet|MalaCards C4084773 Bothered by weight gain C1963119 Stomach ulcer adverse event HSDN C1384666 Decreased hearing C0033817 Pseudomonas infections HSDN C0030975 Disorders perception C0014877 Esotropia HSDN C1279888 Proteinuria of undiagnosed cause C4041080 Neurocognitive disorders HSDN C0022346 Yellow skin C0031154 Peritonitis HSDN C4085642 Level of joint stiffness C1844934 Arthrogryposis multiplex congenita, distal, x-linked OrphaNet|HPO C4085661 Usual severity nausea C0162739 Hellp syndrome HSDN C0242936 Center pain C0020476 Hyperlipoproteinemias HSDN C0231528 Muscle pain generalized C1864997 Majeed syndrome OrphaNet|HPO|MalaCards C0020615 Hypoglycemia nos C1846284 Glucocorticoid deficiency 2 MalaCards C1963281 Vomiting adverse event C0024232 Lymphatic metastasis HSDN C2132198 Abnormal blistering of the skin C0026755 Multiple carboxylase deficiency OrphaNet|MalaCards C0040034 Thrombocytopenia C3151443 Dyskeratosis congenita, autosomal dominant 2 MalaCards C1145670 Failure respiratory C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C0030552 Paralysis partial C0085661 Onycholysis HSDN C0011991 Loose stools C0282207 Cronkhite-canada syndrome OrphaNet|UMLS|MalaCards C3539889 Pelvic pain increasing in severity C2706915 Language:-:point in time:^patient:- HSDN C0241210 Speaking delay C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0349588 Stature short C2932714 Pontocerebellar hypoplasia type 2 MalaCards C2919142 Short stature adverse event C1833792 Oslam syndrome OrphaNet|MalaCards C0233844 Awkwardness C0022336 Creutzfeldt-jakob disease MalaCards C2024878 Cardiovascular surgery result: dyspnea C0032064 Plague HSDN C0009398 Color vision defects C0271092 Progressive cone dystrophy (without rod involvement) OrphaNet|HPO|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0014461 Granuloma eosinophilic MalaCards C4085211 Pain distress question C0036918 Sexually transmitted diseases, viral HSDN C0812426 Kidney problem C0022672 Acute kidney tubular necrosis UMLS C0241210 Speaking delay C0010324 Crigler najjar syndrome, type 1 MalaCards|HPO C0026884 Muteness C0011551 Depersonalisation HSDN C0013404 Respiratory difficulty C0080040 Polio post syndrome HSDN C0022346 Yellow skin C1266018 Hepatocellular carcinoma, scirrhous UMLS C0042420 Vasovagal episode C0006384 Bundle-branch block HSDN C0036659 Sensation disorder C0040438 Ectopic tooth eruption HSDN C1963086 Confusion adverse event C0036980 Shock, cardiogenic HSDN C0026826 High muscle tone C1963088 Cystitis adverse event HSDN C4084767 Bothered by vomiting C0022116 Ischemia HSDN C0041667 Low weight C0265252 Coffin-lowry syndrome MalaCards|HPO C1962962 Hyperpigmentation adverse event C0015625 Fanconi anemia MalaCards C0027498 Nausea vomiting C0001403 Addison disease OrphaNet C1557397 Adverse event associated with pain C1656583 Rosacea HSDN C0009676 Confusion state C0012746 Dissociative disorder HSDN C4084773 Bothered by weight gain C0026848 Myopathy HSDN C0034933 Abnormal reflexes C0006818 Campylobacter infection HSDN C0018681 Headache, cephalalgia C3494559 Intractable allergic migraine UMLS C0019825 Voice hoarseness C1855606 Burton syndrome MalaCards C0030975 Disorders perception C0020538 Hypertensive disease HSDN C2919142 Short stature adverse event C4014343 Mental retardation, autosomal recessive 42 MalaCards C0030193 Sense of pain C1552262 Nurse practitioner - family HSDN C4084766 Vomiting C0027625 Circulating neoplastic cells HSDN C0812426 Kidney problem C0749879 Uremia symptomatic UMLS C0015469 Facial paralysis C0007570 Celiac disease HSDN C4084726 Distress cough C1800706 Idiopathic pulmonary fibrosis MalaCards|HSDN C0030552 Paralysis partial C0001733 Afibrinogenemia HSDN C4085317 Diarrhea frequency C0037073 Sigmoid neoplasms HSDN C0033377 Caudal displacement C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C2237041 Shox gene with short stature C0265287 Acromicric dysplasia HPO C0019825 Voice hoarseness C0031347 Pharyngeal neoplasms HSDN C4084766 Vomiting C0033054 Prenatal exposure delayed effects HSDN C1963091 Diarrhea adverse event C0027813 Neuritis HSDN C0152169 Colic renal C0740394 Hyperuricemia HSDN C2315100 Pediatric failure to thrive C1859974 Glucocorticoid deficiency 1 HPO C0018777 Deafness, conductive C0022893 Otitis interna HSDN C0043094 Weight gain C0007762 Cerebellar neoplasms HSDN C4084767 Bothered by vomiting C0023530 Leukopenia HSDN C4084802 Usual severity diarrhea C2937225 Biotin deficiency disease MalaCards C4084768 Usual severity vomiting C0043528 Zoonoses HSDN C0026821 Cramp C0018799 Heart diseases HSDN C3463815 Feel fatigue C0017921 Glycogen storage disease type ii HSDN C0042798 Vision dim C1836603 Foveal hypoplasia and anterior segment dysgenesis HPO C0003811 Cardiac rhythm disturbance C0268060 Juvenile hemochromatosis MalaCards C0018772 Deafness C0029420 Osteochondritis HSDN C0040822 D tremors C1860808 Triosephosphate isomerase deficiency UMLS C2024893 Cardiovascular surgery result: fatigue C0007095 Carcinoid tumor HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0041318 Tuberculosis, meningeal HSDN C4042891 Sleep wake disorders C0005686 Urinary bladder diseases HSDN C0035078 Failure kidney C0023241 Legionnaires' disease MalaCards C0020615 Hypoglycemia nos C1968739 Glycogen storage disease iiia HPO C0349588 Stature short C0265251 Oto-palato-digital syndrome type 1 MalaCards C0023012 Delay language C2675336 Duplication 15q11-q13 syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0007771 Intracranial arteriosclerosis HSDN C4085211 Pain distress question C1262206 Iliotibial band syndrome HSDN C4084773 Bothered by weight gain C0026640 Mouth neoplasms HSDN C0023014 Developmental disorder language C2936346 22q11 deletion syndrome HSDN C0026821 Cramp C0007001 Carbohydrate metabolism, inborn errors HSDN C2128960 Middle-night awakening with a sore throat C0393761 Fitful sleep UMLS C0007398 Catatonic C0018799 Heart diseases HSDN C2984057 Have nausea C0019195 Hepatitis, viral, human HSDN C2237041 Shox gene with short stature C0268225 Aspartylglucosaminuria MalaCards|HPO C1963093 Dizziness adverse event C0086543 Cataract nos HSDN C3887873 Hearing loss C0032962 Pregnancy complications HSDN C0231528 Muscle pain generalized C1565489 Renal insufficiency HSDN C0013604 Edematous C0015732 Fecal incontinence HSDN C2315100 Pediatric failure to thrive C1704421 Skin pigmentation disorder HSDN C2911645 Weight loss adverse event C0018021 Goiter HSDN C0151786 Weakness muscle C4050613 Anxiety scale (basc-2) HSDN C0020672 Body temperature decreased C0043049 Water intoxication HSDN C0040034 Thrombocytopenia C0036202 Sarcoidosis OrphaNet|HPO|MalaCards C0030193 Sense of pain C0042847 Vitamin b 12 deficiency HSDN C4084776 Weight loss C0002016 Aleutian mink disease DiseaseOntology|MalaCards C2911647 Weight gain adverse event C0011884 Diabetic retinopathy HSDN C0011175 Deficient fluid volume C1282908 De vaal's syndrome MalaCards|HPO C2315100 Pediatric failure to thrive C0038644 Sudden infant death syndrome HSDN C0018681 Headache, cephalalgia C0742078 Mass lesion of brain UMLS C1557397 Adverse event associated with pain C1527298 Dysentery, bacillary HSDN C0497247 Blood pressure elevation C0001627 Congenital adrenal hyperplasia OrphaNet C3539022 Pelvic pain decreasing in severity C2936631 Complaint, subjective health HSDN C0557874 Global developmental delay C1859566 Bardet-biedl syndrome 8 MalaCards|HPO C0013604 Edematous C0007570 Celiac disease HSDN C0349588 Stature short C0270972 Cornelia de lange syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0473129 Diarrhea after git surgery C0274311 Complication of treatment, operative procedure UMLS C4085548 Usual severity dizziness C2936631 Complaint, subjective health HSDN C3815497 Cough C0022116 Ischemia HSDN C0012833 Dizzy C0042170 Uveomeningoencephalitic syndrome HSDN C0023380 Lethargy C0268581 Holocarboxylase synthetase deficiency MalaCards|HPO|UMLS C0005745 Blepharoptosis C1867437 Ptosis, strabismus, and ectopic pupils MalaCards C0018524 Hallucinate C0023522 Leukodystrophy, metachromatic MalaCards|HPO C2984058 Have pain C0036917 Sexually transmitted diseases, bacterial HSDN C1962972 Proteinuria adverse event C0029456 Osteoporosis HSDN C0032285 Pneum C0016627 Avian influenza DiseaseOntology|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0036117 Salmonella infections HSDN C0007758 Cerebellar ataxia C1848412 Trichothiodystrophy with sun sensitivity HPO C0011991 Loose stools C1366464 F9 gene HSDN C3539890 Pelvic pain causes awakening at night C0027095 Myosarcoma HSDN C0020455 Hypergammaglobulinemia C0836924 Thrombocytosis HSDN C0042798 Vision dim C3887937 Cone dystrophy 5, x-linked MalaCards C0000737 Abdomen pain C0035229 Respiratory insufficiency HSDN C0857305 Thrombocytopenia purpura C0344315 Depressed mood HSDN C0018524 Hallucinate C0038220 Status epilepticus HSDN C3815497 Cough C0037579 Soft tissue neoplasms HSDN C0020305 Fetal edema C0019284 Diaphragmatic hernia HSDN C0424755 Fever symptoms C0026769 Multiple sclerosis HSDN C4042891 Sleep wake disorders C0011615 Dermatitis, atopic HSDN C4085317 Diarrhea frequency C0008733 Chylothorax HSDN C0018991 Paralysis one side of body C0011071 Sudden death HSDN C0018681 Headache, cephalalgia C0271972 Thiamine-responsive megaloblastic anemia MalaCards C0018772 Deafness C1853566 Genitopatellar syndrome MalaCards|HPO C3541349 Syncope C0282607 Vascular neoplasms HSDN C0239574 Fever low grade C2931854 Allergic bronchopulmonary mycosis MalaCards C3815497 Cough C0018671 Head and neck neoplasms HSDN C4084802 Usual severity diarrhea C0024215 Lymphangiectasis, intestinal OrphaNet|MalaCards C2203646 Jaundice C0022116 Ischemia HSDN C4084773 Bothered by weight gain C0206255 Malaria vaccine HSDN C0036572 Convulsion C0243026 Sepsis HSDN C1962956 Flatulence adverse event C0236969 Substance-related disorders HSDN C0557874 Global developmental delay C0265316 Neurocutaneous syndromes MalaCards C0917816 Deficiency mental C1849929 Pfeiffer palm teller syndrome MalaCards C2315100 Pediatric failure to thrive C0010709 Cyst HSDN C0004604 Pain back C0022976 Animal gait disorder HSDN C0040822 D tremors C0010674 Cystic fibrosis HSDN C0234146 Absent reflex C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C0027497 Queasy C0003864 Arthritis HSDN C0013404 Respiratory difficulty C0155789 Bleeding esophageal varix UMLS C0233514 Behavior abnormal C1860518 Vasculopathy, retinal, with cerebral leukodystrophy OrphaNet|HPO|MalaCards C0039231 Heartbeats increased C2931660 Autosomal recessive fructose 1, 6-diphosphatase deficiency MalaCards C0040460 Dental pain C3810814 Myocardial infarction ecg assessment HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0017658 Glomerulonephritis HSDN C0036572 Convulsion C0149514 Bronchitis acute HSDN C3665346 Loss sight C1850764 Epilepsy, progressive myoclonic 2b HPO C0015469 Facial paralysis C1836460 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 MalaCards|HPO C0043094 Weight gain C0019557 Hip fx HSDN C0012833 Dizzy C0520754 Posttraumatic vertigo, nos UMLS C0013604 Edematous C0025500 Mesothelioma HSDN C0028081 Night sweat C1336487 Stage i hodgkin's disease lymphocyte depletion type above the diaphragm UMLS C4085862 Bothered by nausea C0460137 Push down or depress HSDN C4085222 Nausea C0003838 Arterial occlusive diseases HSDN C4085211 Pain distress question C0029421 Osteochondritis dissecans HSDN C0013604 Edematous C0032650 Baker's cyst HSDN C0270948 Neurogenic muscular atrophy C1856302 Gsd iv, nonprogressive hepatic HPO C4085317 Diarrhea frequency C0037299 Skin ulcer HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0010674 Cystic fibrosis HSDN C0242936 Center pain C0018552 Hamartoma HSDN C1836296 Lower extremity weakness C1847582 Lipodystrophy with congenital cataracts and neurodegeneration HPO C1069915 Vertigo C0271270 Oculovestibuloauditory syndrome MalaCards C1557397 Adverse event associated with pain C1522137 Hypertriglyceridemia result HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024115 Lung diseases HSDN C4085222 Nausea C3541306 Plasmodium measurement HSDN C0027066 Myoclonic jerking C1839130 Dystonia 3, torsion, x-linked HPO|UMLS C0349588 Stature short C1510479 Neuralgic amyotrophy MalaCards|HPO C0002622 Amnesias C1854369 Spinocerebellar ataxia 14 MalaCards C0919596 Fluctuating consciousness C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards|UMLS C0013604 Edematous C0018824 Heart valve disease HSDN C4084766 Vomiting C1546635 Specimen source codes - fistula HSDN C0575081 Abnormal gait C3538999 Dystonia 23 MalaCards C4084774 Have weight loss C0344434 Atrial fibrillation ecg HSDN C4085317 Diarrhea frequency C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C2237041 Shox gene with short stature C0268556 Saccharopinuria MalaCards|HPO C1963064 Anxiety adverse event C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C0040264 Ear ringing sound C0011615 Dermatitis, atopic HSDN C3665347 Vision impaired C1833798 Optic nerve aplasia, bilateral HPO C0009806 Constipate C0009241 Cognition disorders HSDN C0018784 Deafness sensorineural C0043253 Trauma blunt HSDN C0037284 Skin lesion C0156147 Crohn's disease of large bowel MalaCards C0878773 Bladder hyperactive C0004096 Asthma HSDN C0009792 Consciousness disorder C0012746 Dissociative disorder HSDN C4084775 Usual severity weight loss C0033923 Psychomotor function HSDN C0012569 Double vision C0752180 Bacterial cns infection HSDN C0039070 Collapse fleeting C0032019 Pituitary neoplasms HSDN C0860603 Anxiety symptom C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0041657 Consciousness loss C0018843 Heat stroke HSDN C2984058 Have pain C0032984 Pregnancy, abdominal HSDN C0015672 Decreased energy C0001546 Adjustment disorders HSDN C4085862 Bothered by nausea C0021359 Infertility HSDN C1963091 Diarrhea adverse event C0009447 Common variable immunodeficiency HPO C1279888 Proteinuria of undiagnosed cause C0032285 Pneumonia HSDN C0149651 Clubbing C1265981 Fibrosis and/or repair abnormality UMLS C0232943 Metromenorrhagia C0008493 Hydatidiform mole, invasive OrphaNet|MalaCards C0012833 Dizzy C0034494 Rabies (disorder) HSDN C0018777 Deafness, conductive C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C0028738 Nystagmus C0751918 Cockayne pelizaeus merzbacher disease MalaCards C3641755 Have constipation C0014849 Esophageal and gastric varices HSDN C0242936 Center pain C0035335 Retinoblastoma HSDN C0035078 Failure kidney C0342790 Carnitine palmitoyl transferase 2 deficiency OrphaNet C4084775 Usual severity weight loss C0014121 Bacterial endocarditis HSDN C4084767 Bothered by vomiting C0268193 Nadh cytochrome b5 reductase deficiency MalaCards|HPO C0242936 Center pain C0206708 Cervical intraepithelial neoplasia HSDN C0036572 Convulsion C2035047 Partial simple motor epilepsy UMLS C3641755 Have constipation C0040136 Thyroid neoplasm HSDN C0231341 Aging premature C0019693 Hiv infections HSDN C4085211 Pain distress question C0152025 Polyneuropathy HSDN C0034933 Abnormal reflexes C1963235 Sick sinus syndrome adverse event HSDN C0015672 Decreased energy C0017152 Gastritis HSDN C0024031 Back pain lower back C1548578 Location characteristic id - smoking HSDN C0009806 Constipate C0025063 Mediastinal neoplasms HSDN C0018965 Blood urine C0334419 Pheochromocytoma, malignant MalaCards C1768507 Yellow nails C0037284 Skin lesion UMLS C0002622 Amnesias C0302148 Blood clot HSDN C4084776 Weight loss C0032763 Post gastrectomy syndrome HSDN C0018772 Deafness C0037278 Skin diseases, infectious HSDN C0012833 Dizzy C1836544 Schindler disease, type i OrphaNet|HPO|MalaCards C1836296 Lower extremity weakness C0025286 Meningioma MalaCards C4084724 Usual severity constipation C0205788 Histiocytoid hemangioma HSDN C0917816 Deficiency mental C2931919 X-linked infantile spasm syndrome MalaCards|HPO C0518090 Frequency of pain question C0029421 Osteochondritis dissecans HSDN C0030193 Sense of pain C0264693 Coronary insufficiency, acute UMLS C0043094 Weight gain C0006840 Candidiasis HSDN C4085210 Usual severity pain C0085094 Head injury closed HSDN C1963281 Vomiting adverse event C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C1963252 Tremor adverse event C0037019 Shy-drager syndrome HSDN C3898969 Have been vomiting C0085207 Gestational diabetes HSDN C2984058 Have pain C0235146 Emotionally high HSDN C1971624 Appetite absent C0007097 Carcinomas HSDN C0022346 Yellow skin C0023904 Liver neoplasms, experimental HSDN C1557397 Adverse event associated with pain C0018946 Hematoma, subdural HSDN C0037316 Not enough sleeping C0004096 Asthma HSDN C0028961 Urine output decreased C0032914 Pre-eclampsia HSDN C4085211 Pain distress question C0013473 Eating disorders HSDN C0039070 Collapse fleeting C0015674 Chronic fatigue syndrome HSDN C0036572 Convulsion C0022806 Kwashiorkor HSDN C4085317 Diarrhea frequency C4050613 Anxiety scale (basc-2) HSDN C0085636 Light sensitivity C0043121 Wernicke encephalopathy HSDN C0017181 Gastrointestinal bleed C1333088 Colonic hamartomatous polyps MalaCards C4085211 Pain distress question C0039981 Thoracic neoplasms HSDN C4085549 Dizziness C0677866 Brain stem neoplasms HSDN C0016204 Fart C0034895 Rectovaginal fistula HSDN C0027796 Neuralgias C0032962 Pregnancy complications HSDN C1963281 Vomiting adverse event C0008625 Chromosome aberrations HSDN C4084767 Bothered by vomiting C0003618 Appetites HSDN C4085210 Usual severity pain C0376154 Skin callus HSDN C4084775 Usual severity weight loss C0041318 Tuberculosis, meningeal HSDN C2024878 Cardiovascular surgery result: dyspnea C0039730 Thalassemia HSDN C0039870 Leanness C1623041 Breast-fed HSDN C2911645 Weight loss adverse event C0342257 Complications of diabetes mellitus HSDN C1962972 Proteinuria adverse event C0017152 Gastritis HSDN C0018775 Hearing loss bilateral C1963274 Vasculitis adverse event HSDN C3641891 Have itch C0040252 Tinea corporis (disorder) MalaCards C1963281 Vomiting adverse event C0007762 Cerebellar neoplasms HSDN C0018926 Emesis bloody C0027643 Neoplasm recurrence, local HSDN C0040822 D tremors C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0041657 Consciousness loss C0338586 Vertebral artery dissection HSDN C0018772 Deafness C3683846 Chromosome 17p deletion syndrome MalaCards C1963064 Anxiety adverse event C1578691 Congenital myxedema MalaCards C2919142 Short stature adverse event C0265565 Congenital pseudoarthrosis of clavicle MalaCards C0349588 Stature short C0394006 Dysequilibrium syndrome OrphaNet|HPO C0030552 Paralysis partial C1849386 Myoglobinuria, acute recurrent, autosomal recessive MalaCards|HPO C0036572 Convulsion C0334123 Histiocytosis, lipoid MalaCards C0040822 D tremors C0268407 Senile cardiac amyloidosis MalaCards C1963281 Vomiting adverse event C3888018 Congenital hyperinsulinism MalaCards C0040822 D tremors C0036357 Psychology, schizophrenic HSDN C2919142 Short stature adverse event C0265240 Goldenhar syndrome OrphaNet|MalaCards C0028738 Nystagmus C2931644 O'donnell pappas syndrome OrphaNet|HPO|MalaCards C0016382 Cutaneous vascular engorgement C1858302 Ectodermal dysplasia/ skin fragility syndrome OrphaNet|HPO|MalaCards C0011168 Disorder deglutition C3150169 Frontotemporal lobar degeneration with tdp43 inclusions, tardbp-related HPO C0242936 Center pain C0031099 Periodontitis HSDN C0036572 Convulsion C0025517 Metabolic diseases HSDN C4085661 Usual severity nausea C0018802 Congestive heart failure HSDN C4084769 Vomiting frequency C0206171 Community acquired infections HSDN C0557874 Global developmental delay C2749559 Methemoglobinemia, type i HPO C4084766 Vomiting C0178282 Hernia of abdominal cavity HSDN C1962962 Hyperpigmentation adverse event C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C0007384 Cataplexy C1858804 Cerebellar ataxia, deafness, and narcolepsy HPO C0022408 Disorder joint C1384665 Hfe gene HPO C0042940 Disorder of voice C0027531 Neck injury HSDN C4084767 Bothered by vomiting C4015130 Inflammatory skin and bowel disease, neonatal, 2 MalaCards C0424755 Fever symptoms C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0151786 Weakness muscle C0035304 Retinal degeneration HSDN C0018681 Headache, cephalalgia C0020676 Hypothyroidism HSDN C0003962 Ascites C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO C4084769 Vomiting frequency C0750394 Wbc low HSDN C0010200 Cough symptom C0014541 Epiglottitis HSDN C0042963 Symptoms vomiting C0001118 Acid base imbalance HSDN C1963252 Tremor adverse event C0023904 Liver neoplasms, experimental HSDN C4084727 Cough frequency C0016627 Avian influenza DiseaseOntology|MalaCards C0240715 Perineal lump C0154064 Carcinoma in situ of anus UMLS C4085661 Usual severity nausea C0027663 Neoplasms, multiple primary HSDN C2024893 Cardiovascular surgery result: fatigue C1706377 Memory device component HSDN C0007758 Cerebellar ataxia C0025149 Medulloblastoma MalaCards|HSDN C4085210 Usual severity pain C0015923 Fetal alcohol syndrome HSDN C1963071 Back pain adverse event C0002726 Amyloidosis HSDN C0242936 Center pain C1962958 Hematoma adverse event HSDN C4084802 Usual severity diarrhea C0020428 Hyperaldosteronism HSDN C0518090 Frequency of pain question C0042164 Uveitis HSDN C4085222 Nausea C0042830 Perception visual HSDN C0013421 Dystonia C0029125 Optic atrophies, hereditary HSDN C0700590 Diaphoresis excessive C0343110 Epidermolytic palmoplantar keratoderma of vorner OrphaNet|HPO C3815497 Cough C3714509 Nutrition disorders HSDN C0013604 Edematous C0016842 Congenital pectus excavatum HSDN C0030193 Sense of pain C0751967 Multiple sclerosis, relapsing-remitting HSDN C0022346 Yellow skin C3826890 Bd-ipmn UMLS C0027796 Neuralgias C0022661 Kidney failure, chronic HSDN C0042963 Symptoms vomiting C0341560 Cyclical vomiting, psychogenic UMLS C1963086 Confusion adverse event C0007361 Cat-scratch disease HSDN C1557397 Adverse event associated with pain C3658267 Prostatic neoplasms, castration-resistant HSDN C0043094 Weight gain C0020459 Hyperinsulinism HSDN C0521532 Diaphragmatic weakness C0006057 Botulisms MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0024636 Malocclusion HSDN C0018991 Paralysis one side of body C0015397 Disorder of eye HSDN C0018681 Headache, cephalalgia C0011881 Diabetic nephropathy HSDN C0042571 Vertigo subjective C0017636 Glioblastoma HSDN C4084769 Vomiting frequency C1847839 Episodic ataxia, type 3 MalaCards C2029884 Hearing loss by exam C0017168 Gastroesophageal reflux disease HSDN C0015469 Facial paralysis C0017653 Glomus tumor HSDN C0027498 Nausea vomiting C0238027 Botulism, infantile MalaCards C0018772 Deafness C0033054 Prenatal exposure delayed effects HSDN C0000737 Abdomen pain C1333762 Gastric cardia adenocarcinoma UMLS C4084776 Weight loss C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0206160 Retic count elevated C0037856 Spermatic cord torsion HSDN C3463815 Feel fatigue C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C4085549 Dizziness C0025202 Melanoma HSDN C3887638 Failure to thrive in infant C3887877 Deficiency of glycerate kinase MalaCards C0036572 Convulsion C3553788 Alternating hemiplegia of childhood 2 MalaCards|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0003868 Arthritis, gouty HSDN C0233794 Memory impaired C0751603 Autosomal recessive hereditary spastic paraplegia MalaCards C0002962 Angina C0022822 Hunchback formed after birth HSDN C0003550 Broca aphasia C0006114 Cerebral edema HSDN C0497406 Over weight C0035126 Reperfusion injury HSDN C0003469 Anxiety disorder C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C1000483 Genus anemia C0023374 Lesch-nyhan syndrome OrphaNet|HPO|MalaCards C1279888 Proteinuria of undiagnosed cause C0003850 Arteriosclerosis HSDN C0034150 Skin purpura C0017563 Gingival diseases HSDN C0349588 Stature short C1849661 Acrootoocular syndrome MalaCards C3898969 Have been vomiting C2718092 Acrospiroma HSDN C1963087 Constipation adverse event C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0021359 Infertility C0010481 Cushing syndrome OrphaNet|HPO C2203646 Jaundice C1306589 Congenital dyserythropoietic anemia, type ii HPO C2048468 Inability to impregnate C3537440 Cystinosis, infantile nephropathic MalaCards C0024031 Back pain lower back C0043254 Injuries penetrating HSDN C0028081 Night sweat C2347747 Adult classical hodgkin lymphoma UMLS C0242936 Center pain C0001429 Adenolymphoma HSDN C0476273 Distress respiratory C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C0018524 Hallucinate C0037019 Shy-drager syndrome HSDN C0009421 Comatose C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0024032 Birth weight subnormal C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0018784 Deafness sensorineural C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C0002962 Angina C0004610 Bacteremia HSDN C0476273 Distress respiratory C0432336 Cutis laxa, recessive, type i HPO C0023885 Liver abscess C0018203 Chronic granulomatous disease MalaCards|HPO C0030794 Pelvis pain C0037397 Behavior social HSDN C0848203 Male pelvic pain C0037369 Smoking HSDN C1963071 Back pain adverse event C0018799 Heart diseases HSDN C0015230 Exanthem C0406707 Basan syndrome OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0020619 Hypogonadism HSDN C0023015 Language handicap C0001175 Acquired immunodeficiency syndrome HSDN C1963091 Diarrhea adverse event C0026946 Mycoses HSDN C4085862 Bothered by nausea C3536715 Aa amyloidosis MalaCards C0413252 Hypothermia due to exposure C0003864 Arthritis HSDN C0242936 Center pain C0015397 Disorder of eye HSDN C0518090 Frequency of pain question C0018922 Hemangiopericytoma HSDN C0152116 Torticollis spasmodic C1846707 Spinocerebellar ataxia 17 OrphaNet|HPO|MalaCards C0024032 Birth weight subnormal C1833104 Diabetes mellitus, permanent neonatal MalaCards|HPO C0013604 Edematous C3495422 Finding relating to sexuality and sexual activity HSDN C0036572 Convulsion C0282193 Iron overload HSDN C0042571 Vertigo subjective C0003838 Arterial occlusive diseases HSDN C0034150 Skin purpura C2713537 Deficiency of platelet glycoprotein 1b HPO C0007398 Catatonic C0221074 Depression, postpartum HSDN C0240735 Personality change C0338451 Frontotemporal dementia HPO|UMLS C4085317 Diarrhea frequency C0205788 Histiocytoid hemangioma HSDN C1963090 Dehydration adverse event C0162510 Caroli disease HPO C0037384 Snore C0314657 Genetic predisposition HSDN C0042798 Vision dim C0205770 Choroid plexus papilloma HPO C4084802 Usual severity diarrhea C0042075 Urologic diseases HSDN C4084788 Have dizziness C0007222 Cardiovascular diseases HSDN C1963063 Anorexia adverse event C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C0020578 Hyperventilate C0024141 Lupus erythematosus, systemic HSDN C0026826 High muscle tone C0796099 Cleft lip-palate with abnormal thumbs and microcephaly MalaCards C0008031 Pain chest C1708998 Metastatic adrenal gland chromaffin neoplasm UMLS C0043094 Weight gain C0040038 Thromboembolism HSDN C0020615 Hypoglycemia nos C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0021568 Bites insect stings HSDN C4084723 Constipation C0005940 Bone diseases HSDN C4084775 Usual severity weight loss C0235974 Pancreatic carcinoma MalaCards C0232498 Abdominal tenderness C0269051 Acute endomyometritis UMLS C0013404 Respiratory difficulty C0206629 Pulmonary blastoma OrphaNet|HSDN|UMLS|MalaCards C0234376 Tremor action C1843264 Dystonia 13, torsion MalaCards C0040264 Ear ringing sound C4085311 Depression - recess HSDN C0413252 Hypothermia due to exposure C0021400 Influenza HSDN C0013405 Dyspnea, paroxysmal C0020542 Pulmonary hypertension HSDN C2242996 Tingling C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0151786 Weakness muscle C0024305 Lymphoma, non-hodgkin HSDN C1963064 Anxiety adverse event C1568248 Usher syndrome, type iii MalaCards|HPO C0221170 Stiffness muscle C0410207 Tubular aggregate myopathy MalaCards|HPO C0013421 Dystonia C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C4050613 Anxiety C0751383 Juvenile neuronal ceroid lipofuscinosis MalaCards C0020673 Hypothermia (central) (local) C0037315 Sleep apnea syndromes HSDN C1557397 Adverse event associated with pain C0032966 Complication, neoplastic pregnancy HSDN C0003467 Angst C0687720 Central diabetes insipidus OrphaNet|MalaCards C1963065 Apnea adverse event C0010356 Cross infection HSDN C0011991 Loose stools C0020635 Hypopituitarism HSDN C0041834 Erythematous condition C0272295 Purpura, rheumatica MalaCards C4084766 Vomiting C0029134 Optic neuritis HSDN C2984058 Have pain C0030581 Parotid neoplasms HSDN C4085317 Diarrhea frequency C0018794 Heart block HSDN C4084766 Vomiting C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C0231807 Dyspnea exertional C2749559 Methemoglobinemia, type i HPO C0039070 Collapse fleeting C0037313 Sleep HSDN C0027497 Queasy C2004491 Cicatrix HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0085096 Peripheral vascular diseases HSDN C0042798 Vision dim C1843815 Newfoundland rod-cone dystrophy MalaCards|HPO C0270846 Astatic seizure C1858672 Generalized epilepsy with febrile seizures plus, type 1 HPO C1963067 Atrial fibrillation adverse event C4015474 Chronic atrial and intestinal dysrhythmia MalaCards C4084723 Constipation C1335686 Neuroendocrine neoplasm of rectum MalaCards C0019209 Large liver C1855102 Methylmalonic aciduria cblb type HPO C1882272 Pain adverse event by ctcae anatomic descriptor C1963090 Dehydration adverse event HSDN C1963091 Diarrhea adverse event C0018378 Guillain-barre syndrome HSDN C0015672 Decreased energy C0521168 Injuries occupational HSDN C0424755 Fever symptoms C0015328 Behavior, exploratory HSDN C0013604 Edematous C0812393 Cancer patients and suicide and depression HSDN C3665492 Pigmentations C1153706 Endometrial adenocarcinoma MalaCards C2984058 Have pain C0024138 Lupus erythematosus, discoid HSDN C0036572 Convulsion C0796147 Acrocallosal syndrome MalaCards|HSDN|HPO|UMLS C0030554 Abnormal sensation C0036601 Self mutilation HSDN C0151786 Weakness muscle C0751967 Multiple sclerosis, relapsing-remitting HSDN C0013421 Dystonia C0342728 3-methylglutaconic aciduria type 1 MalaCards|HPO C1963184 Nystagmus adverse event C3150925 Spastic ataxia 4, autosomal recessive HPO C0018989 Paresis of one side of body C3697126 Hemiparesis as late effect of cerebrovascular disease UMLS C4084768 Usual severity vomiting C1535939 Pneumocystis jiroveci pneumonia HSDN C0041105 Jaw spasm C0220686 Aase smith syndrome OrphaNet|MalaCards C0030193 Sense of pain C0001327 Laryngitis acute HSDN C0239819 Hand edema C0522035 Upper extremity edema UMLS C1557397 Adverse event associated with pain C0039981 Thoracic neoplasms HSDN C3641756 Have diarrhea C0042111 Urticaria pigmentosa OrphaNet|HSDN|MalaCards C0020615 Hypoglycemia nos C0812437 Oculo-dento-digital syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0497579 Genital herpes male HSDN C0013421 Dystonia C1859598 Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia MalaCards|HPO C4084802 Usual severity diarrhea C0001125 Acidosis, lactic HSDN C1963064 Anxiety adverse event C0268275 Tay-sachs disease, ab variant MalaCards C0030552 Paralysis partial C1853925 Spondyloocular syndrome, autosomal recessive MalaCards|HPO C0522224 Palsied C0917890 Pineocytoma MalaCards C0557874 Global developmental delay C0220987 Hereditary orotic aciduria OrphaNet|HPO|MalaCards C0023014 Developmental disorder language C0014549 Tonic-clonic epilepsy HSDN C2024893 Cardiovascular surgery result: fatigue C2945767 Childhood liver cancer MalaCards C0024031 Back pain lower back C0027708 Nephroblastoma HSDN C0042928 Paralysis vocal cord C0018213 Graves disease HSDN C1963137 Hydrocephalus adverse event C0398621 Hypoplasminogenemia MalaCards|HPO C4084775 Usual severity weight loss C0026850 Muscular dystrophy HSDN C0007758 Cerebellar ataxia C0270715 Degenerative diseases, central nervous system UMLS C0860603 Anxiety symptom C0020428 Hyperaldosteronism MalaCards C0232513 Premature tooth loss C0029401 Osteitis deformans HPO C0349489 Fetal hypoxia C0002395 Alzheimer's disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0011875 Diabetic angiopathies HSDN C0019521 Hiccoughs C0153416 Malig neop oth spec part oesop MalaCards C2315100 Pediatric failure to thrive C1319466 Barber say syndrome OrphaNet|HPO|MalaCards C4084788 Have dizziness C0003490 Aortic arch syndrome HSDN C4085210 Usual severity pain C0037313 Sleep HSDN C0003862 Pain joint C0158458 Hallux abductovalgus HSDN C0013604 Edematous C1266101 Thymic epithelial tumor OrphaNet C0018932 Bright red rectal bleeding C1881600 Malignant vipoma MalaCards C0027497 Queasy C0009021 Clonorchiasis DiseaseOntology C0042024 Urine incontinence C0023267 Fibroid tumor HSDN C4084725 Usual severity cough C0007932 Chagas' disease + no organ inv MalaCards C4084767 Bothered by vomiting C0025222 Melena HSDN C1971624 Appetite absent C2931038 Pancreatic carcinoma, familial MalaCards C0042024 Urine incontinence C0175702 Williams syndrome MalaCards|HPO C0427055 Face weakness C3148763 Muscular dystrophy, limb-girdle, type 1e MalaCards C0019214 Hepatosplenomegaly C1837174 Hemophagocytic lymphohistiocytosis, familial, 3 MalaCards|HPO C0018784 Deafness sensorineural C0005586 Bipolar disorder HSDN C0026603 Motion sickness C0002064 Alkalosis, respiratory HSDN C2984057 Have nausea C0007784 Cerebral hemisphere hemorrhage HSDN C3463815 Feel fatigue C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C0587246 Extremity weakness C2749345 Refsum disease, adult, 1 HPO C0042963 Symptoms vomiting C0034494 Rabies (disorder) HSDN C0013456 Pain ear C0000833 Abscess HSDN C4084768 Usual severity vomiting C0750394 Wbc low HSDN C2315100 Pediatric failure to thrive C0009995 Cor triatriatum HSDN C0030193 Sense of pain C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C3887638 Failure to thrive in infant C1970470 Surfactant metabolism dysfunction, pulmonary, 2 (disorder) MalaCards|HPO C1565249 Limitation, mobility C0001145 Acne keloid HSDN C0007859 Pain neck C0036202 Sarcoidosis HSDN C2984057 Have nausea C0020255 Hydrocephalus HSDN C4085211 Pain distress question C0014511 Epithelial cyst HSDN C0007859 Pain neck C0338480 Common migraine HSDN C4085210 Usual severity pain C0013473 Eating disorders HSDN C1549543 Administration method - pain C0206231 Bone malalignment HSDN C0085631 Abnormal excitement C0011551 Depersonalisation HSDN C0727671 Red cross toothache drops C3810814 Myocardial infarction ecg assessment HSDN C0013421 Dystonia C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C1557397 Adverse event associated with pain C0001080 Achondroplasia HSDN C0018991 Paralysis one side of body C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0010200 Cough symptom C0042373 Vascular diseases HSDN C0036572 Convulsion C0042826 Field visual HSDN C0030193 Sense of pain C0022575 Keratoconjunctivitis sicca HSDN C2315100 Pediatric failure to thrive C0268374 Adult junctional epidermolysis bullosa (disorder) OrphaNet|MalaCards C4084724 Usual severity constipation C0004238 Atrial fibrillation HSDN C0424755 Fever symptoms C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C3665347 Vision impaired C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0242670 Chronic vegetative state C0472377 Basal ganglia hemorrhage HSDN C0004093 Asthenia C3714509 Nutrition disorders HSDN C4084774 Have weight loss C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C1549543 Administration method - pain C0358297 Anthrax vaccines HSDN C0030193 Sense of pain C0085417 Epilepsy, complex partial HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020598 Hypocalcemia HSDN C2875627 Eyelid retraction left upper eyelid C0015397 Disorder of eye UMLS C0015230 Exanthem C0221228 Comedone UMLS C4084724 Usual severity constipation C0344490 Sacral agenesis HPO C0004604 Pain back C0009492 Compartment syndromes HSDN C0036572 Convulsion C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0030554 Abnormal sensation C0751792 Trauma, nervous system HSDN C0000737 Abdomen pain C2987397 Gastric carcinoma with lymphoid stroma UMLS C2919142 Short stature adverse event C0796066 Microcephaly-cervical spine fusion anomalies OrphaNet|MalaCards C0018775 Hearing loss bilateral C0265240 Goldenhar syndrome HSDN C0751495 Seizure focal C3150860 Epilepsy, familial adult myoclonic, 3 UMLS C0042755 Virilisation C0017979 Glycosuria HSDN C0424755 Fever symptoms C0087031 Juvenile-onset still disease OrphaNet|HPO|MalaCards C0497247 Blood pressure elevation C0010481 Cushing syndrome OrphaNet|HPO|MalaCards C0027796 Neuralgias C0037313 Sleep HSDN C1549543 Administration method - pain C0752130 Spinal cord ischemia HSDN C4084727 Cough frequency C0002871 Anemia HSDN C0750426 Wbc elevated C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C0029163 Hemorrhage mouth C0017920 Glycogen storage disease type i HSDN C0013395 Indigestion C0036946 Sheep--diseases HSDN C0030193 Sense of pain C1535939 Pneumocystis jiroveci pneumonia HSDN C0013362 Dysarthrias C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C0426579 Anorexia symptom C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C4085317 Diarrhea frequency C0032320 Peritoneal free air HSDN C2096293 Ent surgical result ear vertigo C0011581 Depressive disorder HSDN C0026826 High muscle tone C1855606 Burton syndrome MalaCards C1962956 Flatulence adverse event C0460137 Push down or depress HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016171 Fistula of intestine, excluding rectum and anus HSDN C0011570 Monopolar depression C0010308 Congenital hypothyroidism OrphaNet C0221776 Pain mouth C4075642 Atypical odontalgia UMLS C0007815 Cerebrospinal fluid rhinorrhoea C0006118 Brain neoplasms HSDN C2911645 Weight loss adverse event C0024530 Malaria HSDN C0027498 Nausea vomiting C0085762 Alcohol abuse UMLS C4084766 Vomiting C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C0033377 Caudal displacement C1864871 Chromosome 17q21.31 deletion syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C1833104 Diabetes mellitus, permanent neonatal OrphaNet|HPO|MalaCards C0349588 Stature short C1863732 Spondyloepimetaphyseal dysplasia with multiple dislocations OrphaNet|HPO|MalaCards C0037317 Sleep disturbance C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C0037763 Spasm C0006434 Burn injury HSDN C1962972 Proteinuria adverse event C0032969 Pregnancy in diabetics HSDN C0043094 Weight gain C0008626 Congenital chromosomal disease HSDN C0010200 Cough symptom C0041316 Lymph node tuberculosis DiseaseOntology|MalaCards C0042384 Vasculitis, nonspecific C0008728 Churg-strauss syndrome OrphaNet|MalaCards C4085661 Usual severity nausea C3813607 Infantile gastroesophageal reflux HSDN C0000727 Abdomen acute C0007820 Cerebrovascular disorders HSDN C1961131 Cough adverse event C0034530 Injury radiation HSDN C0034150 Skin purpura C0013295 Duodenal ulcer HSDN C0027796 Neuralgias C1145670 Respiratory failure HSDN C1963252 Tremor adverse event C1846790 Joubert syndrome 4 (disorder) MalaCards C4085548 Usual severity dizziness C0019080 Hemorrhage HSDN C2911645 Weight loss adverse event C0007273 Carotid artery diseases HSDN C1963180 Neck pain adverse event C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1963137 Hydrocephalus adverse event C3711749 Nonsyndromic holoprosencephaly MalaCards C0022107 Fussiness C2985524 Rhabdoid tumor predisposition syndrome MalaCards C0012569 Double vision C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C0000737 Abdomen pain C2981663 Stage 0 distal bile duct cancer UMLS C0451941 Itch scrotum C3839897 Disorder of skin of scrotum UMLS C0036572 Convulsion C1334227 Internal auditory canal meningioma UMLS C0398650 Idiopathic thrombocytopenia purpura C0398650 Immune thrombocytopenic purpura MalaCards C0159063 Other urination abnormality C0042075 Urologic diseases UMLS C0036572 Convulsion C1868599 Parietal foramina 1 MalaCards|HPO C0578048 Pain of cardiovascular structure C4047600 Pain co-occurrent and due to varicose veins of right leg UMLS C3244654 Sore throat brand of benzocaine & menthol C0276357 Swine influenza MalaCards C1557397 Adverse event associated with pain C0014849 Esophageal and gastric varices HSDN C4085210 Usual severity pain C0019621 Histiocytosis, langerhans-cell HSDN C0262384 Chest pain atypical C0268039 Ketoacidosis alcoholic UMLS C0034933 Abnormal reflexes C0031924 Bumps goose HSDN C4084802 Usual severity diarrhea C0016483 Food preferences HSDN C1549543 Administration method - pain C0001969 Alcoholic intoxication HSDN C1279888 Proteinuria of undiagnosed cause C0032965 Pregnancy complications, infectious HSDN C3641756 Have diarrhea C0014591 Epistaxis HSDN C0454644 Delayed language development C1859298 Spinocerebellar ataxia, autosomal recessive 2 OrphaNet|HPO|MalaCards C0011991 Loose stools C0043241 Wound infection HSDN C0015672 Decreased energy C0040034 Thrombocytopenia HSDN C0009792 Consciousness disorder C0151744 Myocardial ischemia HSDN C2911647 Weight gain adverse event C0040583 Tracheal stenosis HSDN C3244654 Sore throat brand of benzocaine & menthol C0024788 Green monkey virus disease DiseaseOntology|MalaCards C0024032 Birth weight subnormal C1414529 Fancc gene HPO C2984057 Have nausea C0037397 Behavior social HSDN C2073625 X-ray of chest: pleural effusion C0340834 Hennekam lymphangiectasia lymphedema syndrome HPO C4085211 Pain distress question C0080233 Tooth loss HSDN C4084766 Vomiting C0020517 Hypersensitivity HSDN C0751837 Gait ataxic C0008928 Cleidocranial dysplasia HSDN C0016199 Pain flank C0206686 Adrenocortical carcinoma UMLS C4084774 Have weight loss C0013990 Pathological accumulation of air in tissues HSDN C1963274 Vasculitis adverse event C3146222 Idiopathic aortitis MalaCards C4085210 Usual severity pain C0003962 Ascites HSDN C0521532 Diaphragmatic weakness C0751335 Scapuloperoneal form of spinal muscular atrophy MalaCards|HPO C3146279 Coma C0027080 Myoglobinuria HSDN C0038002 Spleen enlargement C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C2242996 Tingling C1260409 Myasthenia gravis without acute exacerbation MalaCards C0023380 Lethargy C0026755 Multiple carboxylase deficiency OrphaNet|MalaCards C1963184 Nystagmus adverse event C1275336 Hashimoto-pritzker syndrome MalaCards|HPO C0015468 Face pain C0563150 Catastrophization HSDN C0030552 Paralysis partial C0026975 Myelitis HSDN C0232461 Increased appetite C0022134 Islet cell adenoma MalaCards C1332836 Cancer fatigue C0009566 Complication UMLS C4042891 Sleep wake disorders C0027439 Nasopharyngeal neoplasms HSDN C3641891 Have itch C0030757 Pediculus capitis infestation DiseaseOntology C0231528 Muscle pain generalized C1456660 Monkeypox virus infections MalaCards C0040264 Ear ringing sound C0019562 Von hippel-lindau syndrome MalaCards|HSDN|HPO C4085317 Diarrhea frequency C0518449 Control of hip fracture risk HSDN C0020538 Hbp C1836705 Pseudohyperkalemia, familial, 2, due to red cell leak OrphaNet|HPO|MalaCards C0149793 Transient monocular blindness C0006035 Borrelia infections MalaCards C0027498 Nausea vomiting C2931618 Gestational trophoblastic disease MalaCards C0034933 Abnormal reflexes C0850803 Anaphylaxis (non medication) HSDN C0037316 Not enough sleeping C0344435 Ventricular fibrillation by ecg finding HSDN C0020672 Body temperature decreased C0233629 Thinking and speaking disturbances HSDN C4084768 Usual severity vomiting C0026269 Mitral valve stenosis HSDN C2315100 Pediatric failure to thrive C0015306 Hereditary multiple exostoses OrphaNet|HPO C4084776 Weight loss C1385938 Acanthocephaliasis MalaCards C4084776 Weight loss C0220981 Metabolic acidosis HSDN C2984058 Have pain C0032964 Pregnancy complications, hematologic HSDN C1963281 Vomiting adverse event C0282207 Cronkhite-canada syndrome MalaCards C0007859 Pain neck C0026769 Multiple sclerosis HSDN C0518090 Frequency of pain question C0079218 Fibromatosis, aggressive HSDN C3539889 Pelvic pain increasing in severity C0010692 Cystitis HSDN C4084769 Vomiting frequency C0004364 Autoimmune diseases HSDN C3641756 Have diarrhea C0033054 Prenatal exposure delayed effects HSDN C1963087 Constipation adverse event C0005686 Urinary bladder diseases HSDN C0015230 Exanthem C1384600 Systemic onset juvenile chronic arthritis OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0018800 Cardiomegaly HSDN C0007758 Cerebellar ataxia C0268568 Classic maple syrup urine disease HPO C4084725 Usual severity cough C0009324 Ulcerative colitis HSDN C0027066 Myoclonic jerking C0019829 Hodgkin disease HSDN C4084773 Bothered by weight gain C0032002 Pituitary diseases HSDN C1279888 Proteinuria of undiagnosed cause C0398641 Epstein syndrome (disorder) HPO C1557397 Adverse event associated with pain C2827407 Infectious otitis media HSDN C1850830 Exercise-induced muscle pain C0795887 Chromosome xp21 deletion syndrome MalaCards C0016382 Cutaneous vascular engorgement C1881600 Malignant vipoma MalaCards|HSDN C4042891 Sleep wake disorders C2020541 Strabismus HSDN C0025323 Bleeding menstrual heavy C3280120 Bleeding disorder, platelet-type, 11 MalaCards C2919142 Short stature adverse event C0080178 Spina bifida OrphaNet C1557397 Adverse event associated with pain C0013312 Dupuytren contracture HSDN C4085211 Pain distress question C1963215 Pneumothorax adverse event HSDN C0263531 Flaking nails C0333606 Dystrophies UMLS C0030193 Sense of pain C0025303 Meningococcal infections HSDN C0004134 Dyssynergia C2931092 Maternally inherited leigh syndrome MalaCards C4084784 Diarrhea C0036674 Sensory deprivation HSDN C0013362 Dysarthrias C0221060 Mobius syndrome MalaCards|HSDN C0013390 Cramps menstrual C0282488 Interstitial cystitis HSDN C4084773 Bothered by weight gain C0032965 Pregnancy complications, infectious HSDN C0851578 Disorder sleep C0011175 Dehydration HSDN C4084775 Usual severity weight loss C3714644 Thymus neoplasms MalaCards|HSDN C4085317 Diarrhea frequency C0032131 Plasmacytoma HSDN C0853698 Lymphocytes increased C3541994 Drug hypersensitivity syndrome OrphaNet|MalaCards C0426579 Anorexia symptom C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0030486 Extremity paralysis, lower C0011849 Diabetes mellitus HSDN C0151786 Weakness muscle C0024636 Malocclusion HSDN C1557397 Adverse event associated with pain C0025521 Inborn errors of metabolism HSDN C0007166 Cardiac output decreased C2936331 Sarcoglycanopathies HSDN C2919142 Short stature adverse event C0796102 Digito-orofacial syndrome ix MalaCards C0019572 Hairiness C0006434 Burn injury HSDN C0085128 Cardiac output elevated C0349464 Wernicke-korsakoff syndrome HSDN C0030218 Palatal paralysis C1290856 Head disorders UMLS C0030193 Sense of pain C0021933 Intussusception HSDN C0349588 Stature short C0497327 Dementia MalaCards C0040485 Wryneck C1962963 Osteoporosis adverse event HSDN C2984057 Have nausea C0035242 Respiratory tract diseases HSDN C0030193 Sense of pain C3668816 Inflammation of non-human mammary gland HSDN C4042891 Sleep wake disorders C0237873 Physiological sexual disorders HSDN C0042798 Vision dim C1855675 Arima syndrome OrphaNet C4084773 Bothered by weight gain C0018891 Animal helminthiases HSDN C1963281 Vomiting adverse event C0017416 Genital neoplasms, female HSDN C3641756 Have diarrhea C0002792 Anaphylaxis HSDN C0018777 Deafness, conductive C0265240 Goldenhar syndrome MalaCards C0009460 Communication impairment C0036346 Schizophrenia, childhood HSDN C2024893 Cardiovascular surgery result: fatigue C1290398 Cerebral arterial aneurysm HSDN C0028961 Urine output decreased C0027651 Tumor HSDN C0018784 Deafness sensorineural C1845546 Fg syndrome 4 (disorder) MalaCards|HPO C0004604 Pain back C1956346 Coronary artery disease HSDN C1963249 Tinnitus adverse event C1854146 Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 HPO C4085211 Pain distress question C0041954 Ureteral diseases and syndromes HSDN C0024031 Back pain lower back C0027765 Nervous system disorder HSDN C0002962 Angina C0007784 Cerebral hemisphere hemorrhage HSDN C0150055 Pain chronic C0018801 Heart failure HSDN C0018784 Deafness sensorineural C0038663 Suicide attempt HSDN C3463815 Feel fatigue C0001418 Adenocarcinoma HSDN C0033774 Skin pruritus C0004238 Atrial fibrillation HSDN C0002622 Amnesias C0008370 Cholestasis HSDN C3539891 Pelvic pain to the rear C0281865 Hip injury HSDN C0038990 Sweats C3539003 Neuropathy, hereditary sensory and autonomic, type vi MalaCards C4084784 Diarrhea C0034494 Rabies (disorder) OrphaNet|HSDN|MalaCards C0042963 Symptoms vomiting C1868690 Hypoadrenocorticism, familial UMLS C0034933 Abnormal reflexes C0078888 Accelerated idioventricular rhythm HSDN C2315100 Pediatric failure to thrive C0004352 Autistic disorder HSDN C0010520 Skin cyanosis C0015480 Disorder factitious HSDN C0040822 D tremors C2931395 Bulbospinal neuronopathy, x-linked recessive HPO C1549543 Administration method - pain C0006262 Bronchial fistula HSDN C0920040 Paresis ulnar nerve C3203709 Peripheral nerve paresis UMLS C4084768 Usual severity vomiting C0003873 Rheumatoid arthritis HSDN C0034150 Skin purpura C0015397 Disorder of eye HSDN C4085211 Pain distress question C0022735 Klinefelter syndrome HSDN C1279888 Proteinuria of undiagnosed cause C1963137 Hydrocephalus adverse event HSDN C4084776 Weight loss C4045991 Perihilar cholangiocarcinoma MalaCards C0019079 Bloody sputum C1868703 Bacterial tracheitis HSDN C1145670 Failure respiratory C0271742 Glucocorticoid deficiency with achalasia HPO C4085222 Nausea C0040136 Thyroid neoplasm HSDN C0003910 Articulation disorder C0751843 Aca infarction HSDN C0004604 Pain back C0029118 Opportunistic infections HSDN C1963063 Anorexia adverse event C2984289 Melanoma pathway HSDN C4049644 Depression C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0040264 Ear ringing sound C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4085317 Diarrhea frequency C0015408 Eye injury HSDN C0030232 Color loss C0007932 Chagas' disease + no organ inv MalaCards C4084767 Bothered by vomiting C0025472 Mesenteric vascular occlusion HSDN C0030193 Sense of pain C1269683 Major depressive disorder HSDN C4085661 Usual severity nausea C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0851578 Disorder sleep C1963083 Cholecystitis adverse event HSDN C2984057 Have nausea C0086543 Cataract nos HSDN C0020305 Fetal edema C0220685 Achondrogenesis type 2 OrphaNet|HPO C4085211 Pain distress question C0025061 Disease of mediastinum HSDN C3887873 Hearing loss C0022521 Kartagener syndrome HSDN C4084768 Usual severity vomiting C0009946 Conversion disorder HSDN C3815497 Cough C0015663 Fasting HSDN C4085317 Diarrhea frequency C0035579 Rickets HSDN C0848203 Male pelvic pain C0033046 Premenstrual syndrome HSDN C0235076 Tongue sluggish C0860556 Tongue movement disturbance UMLS C0002965 Crescendo angina C1963119 Stomach ulcer adverse event HSDN C0009806 Constipate C1962963 Osteoporosis adverse event HSDN C3641756 Have diarrhea C0031762 Photosensitivity disorders HSDN C4084802 Usual severity diarrhea C0034362 Q fever HSDN C0042963 Symptoms vomiting C0022593 Keratosis HSDN C0042024 Urine incontinence C0032962 Pregnancy complications HSDN C0013604 Edematous C0032342 Rhus dermatitis HSDN C0231788 Pronated foot C3809753 Mental retardation, autosomal recessive 38 MalaCards|UMLS C3539896 Pelvic pain occurs with urination C0010068 Coronary heart disease HSDN C0518090 Frequency of pain question C0030849 Penile neoplasms HSDN C0009806 Constipate C4225351 White-sutton syndrome UMLS C0151889 Reflexes tendon increased C2936879 Spastic paraplegia 36, autosomal dominant MalaCards C4085211 Pain distress question C0018128 Graft occlusion, vascular HSDN C3463815 Feel fatigue C1366535 Avp gene HSDN C1000483 Genus anemia C0700095 Central neuroblastoma MalaCards C0039870 Leanness C0033348 Language program HSDN C0085631 Abnormal excitement C0338451 Frontotemporal dementia HSDN C0002965 Crescendo angina C1963138 Hypertension adverse event HSDN C0151686 Growth retardation C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards C0023015 Language handicap C0003467 Anxiety HSDN C4084773 Bothered by weight gain C0024895 Bovine mastitis HSDN C4084767 Bothered by vomiting C0026764 Multiple myeloma HSDN C0476273 Distress respiratory C0265279 Kniest dysplasia MalaCards|HPO|UMLS C0231218 Malaise generalized C0006142 Malignant neoplasm of breast UMLS C2315100 Pediatric failure to thrive C1449842 Pseudohypoaldosteronism, type i, autosomal dominant HPO C1963091 Diarrhea adverse event C2749484 Neuroblastoma, susceptibility to HPO C0151686 Growth retardation C1832362 Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis MalaCards C3887873 Hearing loss C0004935 Animal ethology HSDN C2936821 Spinal cerebrospinal fluid leak C1306214 Acth-secreting pituitary adenoma HSDN C0038002 Spleen enlargement C0272199 Familial hemophagocytic lymphocytosis MalaCards C4085211 Pain distress question C0036330 Schistosomiasis mansoni HSDN C3641756 Have diarrhea C0206624 Hepatoblastoma MalaCards C0009676 Confusion state C0020258 Hydrocephalus, normal pressure HSDN C0030552 Paralysis partial C0410226 Congenital myotonic dystrophy MalaCards C1971624 Appetite absent C0276357 Swine influenza MalaCards C0033774 Skin pruritus C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C4085549 Dizziness C3495422 Finding relating to sexuality and sexual activity HSDN C1963249 Tinnitus adverse event C0085094 Head injury closed HSDN C0018784 Deafness sensorineural C0599973 Waardenburg anophthalmia syndrome MalaCards C1549543 Administration method - pain C0024419 Waldenstrom macroglobulinemia HSDN C0018808 Murmur C0035243 Respiratory tract infections HSDN C0016205 Flatulence, eructation, and gas pain C0810319 Other and unspecified gastrointestinal disorders UMLS C2203646 Jaundice C0009404 Colorectal neoplasms HSDN C0151786 Weakness muscle C0796204 Worster-drought syndrome MalaCards C0003862 Pain joint C0002726 Amyloidosis HSDN C1963167 Memory impairment adverse event C3807295 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant MalaCards C0018681 Headache, cephalalgia C2749562 Nadh-cytochrome b5 reductase deficiency, type ii HPO C0007758 Cerebellar ataxia C1850386 Giant axonal neuropathy 1 HSDN C2911645 Weight loss adverse event C3665624 Serum calcium below normal HSDN C4084784 Diarrhea C0032269 Pneumococcal infections HSDN C2984058 Have pain C0038536 Subcutaneous emphysema HSDN C3641756 Have diarrhea C2004491 Cicatrix HSDN C4084776 Weight loss C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0011880 Diabetic ketoacidosis HSDN C0016382 Cutaneous vascular engorgement C0030783 Pellagra HSDN C1279888 Proteinuria of undiagnosed cause C0037199 Sinusitis HSDN C0020615 Hypoglycemia nos C0268059 Neonatal hemochromatosis OrphaNet|MalaCards C1963170 Hypothermia adverse event C0022408 Arthropathy HSDN C0033377 Caudal displacement C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C2203646 Jaundice C1704272 Benign prostatic hyperplasia HSDN C1971624 Appetite absent C0796561 Melanoma vaccines HSDN C4084776 Weight loss C2931279 Hoepffner dreyer reimers syndrome OrphaNet|MalaCards C1384666 Decreased hearing C1861735 Dementia, familial danish HPO C0013428 Painful urination C0862432 Stage iv bladder urothelial carcinoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0040820 Trematode infections HSDN C2032395 Pelvic pain on the left C3495422 Finding relating to sexuality and sexual activity HSDN C4084775 Usual severity weight loss C0040128 Thyroid diseases HSDN C0040822 D tremors C2930798 Alexanders leukodystrophy MalaCards C4084775 Usual severity weight loss C0220847 C hepatitis virus HSDN C4084725 Usual severity cough C0221757 Alpha 1-antitrypsin deficiency HSDN C0030193 Sense of pain C0036830 Serum sickness HSDN C4084724 Usual severity constipation C0431406 Asymmetric crying face association OrphaNet|HPO C4085862 Bothered by nausea C1705811 Terminology role entity HSDN C0018808 Murmur C0034929 Reflex HSDN C1963087 Constipation adverse event C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C0002962 Angina C2931785 Juvenile dermatomyositis MalaCards C0231712 Gait waddling C3148763 Muscular dystrophy, limb-girdle, type 1e MalaCards|HPO|UMLS C0557874 Global developmental delay C2931008 Congenital disorder of glycosylation type 2a MalaCards C0018681 Headache, cephalalgia C1332962 Childhood cerebral ependymoblastoma UMLS C4084767 Bothered by vomiting C0029458 Osteoporosis, postmenopausal HSDN C0009398 Color vision defects C0812393 Cancer patients and suicide and depression HSDN C0026858 Musculoskeletal pain C0002796 Anaplasmataceae infection HSDN C0031911 Pigment deposition C0021828 Intestinal atresia MalaCards C0036572 Convulsion C0011127 Pressure ulcer HSDN C0033774 Skin pruritus C0013295 Duodenal ulcer HSDN C3887638 Failure to thrive in infant C3543867 Collodion fetus MalaCards C0015672 Decreased energy C0003467 Anxiety UMLS C0155552 Hearing loss mixed C1302808 Myopericytoma HSDN C0242936 Center pain C0022362 Jaw diseases HSDN C3829611 Nausea frequency C0008066 Child behavior disorders HSDN C1963184 Nystagmus adverse event C1841721 Achromatopsia 4 HPO C4085222 Nausea C0025063 Mediastinal neoplasms HSDN C4085210 Usual severity pain C0282488 Interstitial cystitis OrphaNet|MalaCards C0030552 Paralysis partial C0162671 Melas syndrome OrphaNet|HSDN|HPO|MalaCards C0000737 Abdomen pain C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0700078 Deep tendon reflex decrease C1838492 Spinal muscular atrophy, distal, congenital nonprogressive (disorder) HPO C0042025 Urinary incontinence stress C0022408 Arthropathy HSDN C0037763 Spasm C0023066 Laryngismus UMLS C2237041 Shox gene with short stature C1855861 Glycogen storage disease 0, liver MalaCards C0043094 Weight gain C0553580 Ewings sarcoma HSDN C0015469 Facial paralysis C0004352 Autistic disorder HSDN C0042755 Virilisation C0027051 Myocardial infarction HSDN C0085636 Light sensitivity C0432328 Xeroderma pigmentosum, variant form OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0006110 Brain death HSDN C0020615 Hypoglycemia nos C1865145 Congenital disorder of glycosylation type 1b OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0003490 Aortic arch syndrome HSDN C0015938 Fetal macrosomia C0030445 Obstetric paralysis HSDN C1963093 Dizziness adverse event C0016542 Foreign body HSDN C0020538 Hbp C2939462 Immunoglobulin deposition disease MalaCards C0030200 Intractable pain C0919267 Ovarian neoplasm HSDN C0042384 Vasculitis, nonspecific C3463916 Complement factor i (c3 inactivator) deficiency MalaCards C0270948 Neurogenic muscular atrophy C0265339 Borjeson-forssman-lehmann syndrome MalaCards|HPO C0149745 Ulcer mouth C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C0042928 Paralysis vocal cord C0012644 Animal disease models HSDN C4084788 Have dizziness C0029401 Osteitis deformans HSDN C0018681 Headache, cephalalgia C0011875 Diabetic angiopathies HSDN C1963281 Vomiting adverse event C0042870 Vitamin d deficiency HSDN C0030552 Paralysis partial C0238357 Hyperkalemic periodic paralysis HSDN C0242936 Center pain C0030499 Parasitic diseases HSDN C3898969 Have been vomiting C0015934 Fetal growth retardation HSDN C0018681 Headache, cephalalgia C0013274 Patent ductus arteriosus HSDN C1963170 Hypothermia adverse event C0042769 Virus diseases HSDN C2237041 Shox gene with short stature C0878683 Pituitary dwarfism type 3 MalaCards|HPO C4085210 Usual severity pain C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0151786 Weakness muscle C0017409 Herpes zoster oticus HSDN C0221232 Welts C0413246 Latex-induced angio-edema-urticaria UMLS C4085211 Pain distress question C1720983 Channelopathies HSDN C0004134 Dyssynergia C1970180 Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation HPO|UMLS C0011175 Deficient fluid volume C1855116 Methylmalonic aciduria, mut(-) type HPO C0232466 Feeding difficulty C1842466 Uniparental disomy, paternal, chromosome 14 MalaCards C0751265 Learning disability C0795888 Autism, susceptibility to, x-linked 4 MalaCards C4084802 Usual severity diarrhea C0035204 Respiration disorders HSDN C3463815 Feel fatigue C0032966 Complication, neoplastic pregnancy HSDN C0277959 Hair coarseness C0268355 Cutis laxa, autosomal recessive, type iia MalaCards|HPO C0033774 Skin pruritus C0006079 Bowen's disease HSDN C2700617 Irritation - emotion C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C0020672 Body temperature decreased C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084767 Bothered by vomiting C0338480 Common migraine HSDN C0042963 Symptoms vomiting C0037198 Sinus thrombosis, intracranial HSDN C3641756 Have diarrhea C0242216 Biliary calculi HSDN C0242936 Center pain C0271051 Macular retinal edema HSDN C0039070 Collapse fleeting C0018794 Heart block MalaCards C3898969 Have been vomiting C1855109 Methylmalonic aciduria cbla type HPO C1963184 Nystagmus adverse event C4015505 Spinocerebellar ataxia, autosomal recessive 18 MalaCards C1549543 Administration method - pain C0024692 Mandible fracture HSDN C3665347 Vision impaired C0024523 Malabsorption syndrome MalaCards C0424755 Fever symptoms C1299919 Enteric coccidiosis HSDN C0013404 Respiratory difficulty C0276572 Aids with dyspnea UMLS C0042571 Vertigo subjective C0007194 Hypertrophic cardiomyopathy HSDN C0036572 Convulsion C1865974 Hypomagnesemia 1, intestinal MalaCards|HPO|UMLS C0013421 Dystonia C0026267 Mitral valve prolapse syndrome HSDN C0151889 Reflexes tendon increased C1848922 Hexosaminidase alpha-subunit deficiency (variant b) OrphaNet|MalaCards C4085862 Bothered by nausea C0275911 Tuberculosis of intestines MalaCards C1838869 Proximal neurogenic muscle weakness C2750537 Myopathy, actin, congenital, with cores HPO C0000727 Abdomen acute C0220981 Metabolic acidosis HSDN C0023012 Delay language C0795907 Conotruncal anomaly face syndrome MalaCards C4084725 Usual severity cough C0032319 Pneumopericardium HSDN C0018681 Headache, cephalalgia C0004052 Aspiration of vomitus HSDN C0026826 High muscle tone C0080024 Piebaldism HSDN C2919142 Short stature adverse event C3150674 Chromosome 15q24 deletion syndrome MalaCards|HPO C0039070 Collapse fleeting C1841658 Progressive familial heart block, type ii MalaCards|UMLS C4084766 Vomiting C0032371 Poliomyelitis MalaCards|HSDN C0007166 Cardiac output decreased C0035126 Reperfusion injury HSDN C0035229 Respiratory function impaired C1968556 Encephalopathy, neonatal severe, due to mecp2 mutations HPO C1549543 Administration method - pain C0263843 Band iliotibial syndromes HSDN C2984057 Have nausea C3887662 Intraspinal neoplasm HSDN C0039070 Collapse fleeting C0752347 Lewy body disease HSDN C4084724 Usual severity constipation C0020550 Hyperthyroidism HSDN C1961131 Cough adverse event C0585442 Osteosarcoma of bone HSDN C0917816 Deficiency mental C0796282 Cataract-hypertrichosis-mental retardation syndrome OrphaNet|MalaCards C2919142 Short stature adverse event C2931622 Ring chromosome 7 OrphaNet|MalaCards C3641755 Have constipation C0001807 Aggressive behavior HSDN C4084767 Bothered by vomiting C1963266 Uveitis adverse event HSDN C4084773 Bothered by weight gain C0036323 Schistosomiasis HSDN C4084775 Usual severity weight loss C0162534 Prion diseases HSDN C1549543 Administration method - pain C1412004 Tumor of the pineal region HSDN C0022346 Yellow skin C0025521 Inborn errors of metabolism HSDN C0018991 Paralysis one side of body C0003490 Aortic arch syndrome HSDN C0917816 Deficiency mental C1855057 Ataxia-telangiectasia variant v2 HPO C4085548 Usual severity dizziness C0042075 Urologic diseases HSDN C0242936 Center pain C0002514 Amino acid metabolism, inborn errors HSDN C0917816 Deficiency mental C3541340 Pontine tegmental cap dysplasia MalaCards C1549543 Administration method - pain C0012817 Diverticulum HSDN C4084775 Usual severity weight loss C0062527 Hepatitis b vaccine HSDN C0015469 Facial paralysis C4015513 Myopathy, isolated mitochondrial, autosomal dominant MalaCards C2984057 Have nausea C0205788 Histiocytoid hemangioma HSDN C3665346 Loss sight C3150191 Coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities MalaCards|HPO C1963063 Anorexia adverse event C0011581 Depressive disorder HSDN C0003862 Pain joint C0011849 Diabetes mellitus HSDN C3539896 Pelvic pain occurs with urination C0019066 Nontraumatic hemoperitoneum HSDN C0221166 Paraparesis C0220654 Meningeal carcinomatosis HSDN C4084784 Diarrhea C0012242 Digestive system disorders HSDN C0011206 Delirium acute C0007682 Cns disorder HSDN C0013404 Respiratory difficulty C0030824 Allergy to penicillin UMLS C0027498 Nausea vomiting C2936797 Acid cholesteryl ester hydrolase deficiency, type 2 OrphaNet C3887873 Hearing loss C0001580 Adolescent behavior HSDN C0042798 Vision dim C1857779 Senior-loken syndrome 6 MalaCards|HPO C4085210 Usual severity pain C0162637 Strongylida infections HSDN C4084774 Have weight loss C2931638 Chromosome 8, monosomy 8p23 1 MalaCards C2315100 Pediatric failure to thrive C1970470 Surfactant metabolism dysfunction, pulmonary, 2 (disorder) MalaCards|HPO C0241165 Skin thickening C0265311 Leri pleonosteosis syndrome MalaCards C1963093 Dizziness adverse event C0006277 Bronchitis HSDN C0577572 Mass of musculoskeletal structure C2960769 Cholesterin granuloma of mastoid UMLS C0424755 Fever symptoms C0013884 Filarial elephantiases DiseaseOntology|HSDN C0026884 Muteness C0033348 Language program HSDN C0020903 Illusion C0338480 Common migraine HSDN C4042891 Sleep wake disorders C1962963 Osteoporosis adverse event HSDN C0040485 Wryneck C0003803 Arnold chiari malformation HSDN C4084788 Have dizziness C0026764 Multiple myeloma HSDN C1961131 Cough adverse event C0032963 Pregnancy complications, cardiovascular HSDN C0851578 Disorder sleep C0233610 Negativism in catatonia HSDN C0034933 Abnormal reflexes C0038160 Staphylococcal infections HSDN C4084802 Usual severity diarrhea C0036916 Sexually transmitted diseases HSDN C4084724 Usual severity constipation C2673611 Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant HPO C2911645 Weight loss adverse event C0014118 Endocarditis HSDN C4084767 Bothered by vomiting C0018790 Cardiac arrest HSDN C2024878 Cardiovascular surgery result: dyspnea C1457883 Aggressive reaction HSDN C4085317 Diarrhea frequency C1283620 Sucrase-isomaltase deficiency, congenital OrphaNet|HPO|MalaCards C1963170 Hypothermia adverse event C0019348 Herpes simplex infections HSDN C0015672 Decreased energy C0032002 Pituitary diseases HSDN C0423715 Testicular neuralgia C0031121 Neuralgia peripheral UMLS C1549543 Administration method - pain C0006413 Burkitt lymphoma HSDN C0018772 Deafness C0030583 Parotitis HSDN C0039070 Collapse fleeting C0238096 Embolism, paradoxical HSDN C0018524 Hallucinate C0600260 Lung diseases, obstructive HSDN C2984058 Have pain C0238417 Scorpion sting HSDN C0033377 Caudal displacement C1850599 Leigh syndrome due to mitochondrial complex iv deficiency HPO C0150055 Pain chronic C0079631 Interdisciplinary communication HSDN C4084784 Diarrhea C0024788 Green monkey virus disease DiseaseOntology|OrphaNet|MalaCards C2984058 Have pain C0043202 Wolff-parkinson-white syndrome HSDN C0019209 Large liver C0263628 Tumoral calcinosis MalaCards C0020455 Hypergammaglobulinemia C0023434 Chronic lymphocytic leukemia HSDN C1557397 Adverse event associated with pain C1561518 Pleasure - animals raised for recreation HSDN C0011206 Delirium acute C0009952 Febrile convulsions HSDN C4084726 Distress cough C1706004 Anhydrotic ectodermal dysplasias OrphaNet|MalaCards C1557397 Adverse event associated with pain C0275148 Poisoning of animal by plant HSDN C1959630 Eye pain adverse event C3203360 Suppuration HSDN C0036572 Convulsion C0235833 Congenital diaphragmatic hernia HSDN C0241210 Speaking delay C4015558 Temple syndrome MalaCards C0020672 Body temperature decreased C0014121 Bacterial endocarditis HSDN C3829611 Nausea frequency C0521607 Peritoneal fibrosis HSDN C0349588 Stature short C1854470 Mesomelic dysplasia with absent fibulas and triangular tibias OrphaNet|MalaCards C4085642 Level of joint stiffness C0265249 Mietens' syndrome MalaCards C1549543 Administration method - pain C0027877 Neuronal ceroid-lipofuscinoses HSDN C1279888 Proteinuria of undiagnosed cause C0038395 Streptococcal infections HSDN C3539891 Pelvic pain to the rear C0019294 Hernia, inguinal HSDN C1963066 Joint pain adverse event C0494042 Spirillosis MalaCards C0036572 Convulsion C0553730 Calcium pyrophosphate deposition disease MalaCards|HSDN|HPO C0022107 Fussiness C2932716 Pseudohypoparathyroidism type 1c HPO C0020796 Profoundly mentally retarded C2677682 Rett syndrome, zappella variant HPO C0518090 Frequency of pain question C0027658 Neoplasms, germ cell and embryonal HSDN C0015672 Decreased energy C0011127 Pressure ulcer HSDN C0002962 Angina C0003869 Arthritis, infectious HSDN C0032617 High urine output C0002871 Anemia HSDN C1963281 Vomiting adverse event C0013449 Ear neoplasms HSDN C4084775 Usual severity weight loss C0001621 Adrenal gland diseases HSDN C1557397 Adverse event associated with pain C0085083 Ovarian hyperstimulation syndrome HSDN C0016199 Pain flank C1333001 Childhood renal cell carcinoma UMLS C0026884 Muteness C0018920 Hemangioma, cavernous HSDN C2024893 Cardiovascular surgery result: fatigue C0151744 Myocardial ischemia HSDN C0857305 Thrombocytopenia purpura C0032587 Polyradiculoneuropathy HSDN C0557874 Global developmental delay C3553915 Methylmalonic aciduria and homocystinuria, cblj type MalaCards C0031911 Pigment deposition C0024437 Macular degeneration MalaCards C4084774 Have weight loss C0002016 Aleutian mink disease DiseaseOntology|MalaCards C0033377 Caudal displacement C0265205 Robinow syndrome MalaCards C0015672 Decreased energy C1859317 Cataract and cardiomyopathy MalaCards|HPO|UMLS C0557874 Global developmental delay C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C4085211 Pain distress question C0001144 Acne vulgaris HSDN C0518090 Frequency of pain question C0031048 Pericarditis, constrictive HSDN C4085661 Usual severity nausea C0085096 Peripheral vascular diseases HSDN C0022107 Fussiness C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) HPO C4085548 Usual severity dizziness C4084909 Depression subordinate domain HSDN C0011991 Loose stools C3810147 Immunodeficiency 19 MalaCards|UMLS C4085661 Usual severity nausea C0020179 Huntington disease HSDN C0018772 Deafness C4085311 Depression - recess HSDN C0018772 Deafness C1546533 Specimen source codes - abscess HSDN C0002965 Crescendo angina C0014836 Escherichia coli infections HSDN C4084769 Vomiting frequency C0524910 Hepatitis c, chronic MalaCards C0018681 Headache, cephalalgia C0020456 Hyperglycemia HSDN C0030552 Paralysis partial C0013926 Aeroembolism HSDN C0030554 Abnormal sensation C0042373 Vascular diseases HSDN C1971624 Appetite absent C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C0013911 Emaciate C0032002 Pituitary diseases HSDN C0003126 Smell loss C1835793 Kallmann syndrome 2 with cleft lip or palate HPO C3146279 Coma C1550639 Specimen type - fistula HSDN C0027796 Neuralgias C0011581 Depressive disorder HSDN C4085317 Diarrhea frequency C0221752 Rbc urine HSDN C0036572 Convulsion C0042487 Venous thrombosis HSDN C0004134 Dyssynergia C0023788 Whipple disease MalaCards|HSDN C0042571 Vertigo subjective C0036690 Septicemia HSDN C1963281 Vomiting adverse event C0018805 Heart injuries HSDN C4084775 Usual severity weight loss C0003128 Anovulation HSDN C0027497 Queasy C0037929 Spinal cord injuries HSDN C0009806 Constipate C1134719 Invasive ductal breast carcinoma HSDN C0427055 Face weakness C2751831 Myopathy, myofibrillar, bag3-related MalaCards|HPO|UMLS C0151686 Growth retardation C0024215 Lymphangiectasis, intestinal OrphaNet|MalaCards C0413252 Hypothermia due to exposure C0027659 Neoplasms, experimental HSDN C0151786 Weakness muscle C0032914 Pre-eclampsia HSDN C0156317 Genital edema male C0578541 Edema trunk UMLS C0033774 Skin pruritus C0020555 Hypertrichosis HSDN C2032396 Pelvic pain on the right C1546602 Specimen source codes - diverticulum HSDN C4084725 Usual severity cough C0025521 Inborn errors of metabolism HSDN C0013362 Dysarthrias C0085292 Stiff-person syndrome HSDN C0518090 Frequency of pain question C0013806 Electroplexy shock therapy HSDN C0039070 Collapse fleeting C1836438 Familial neurocardiogenic syncope MalaCards|UMLS C0018681 Headache, cephalalgia C0035459 Atrophic rhinitis HSDN C1557397 Adverse event associated with pain C0019114 Hemosiderosis HSDN C4084767 Bothered by vomiting C0009404 Colorectal neoplasms HSDN C4085211 Pain distress question C0878588 Sphincter oddi dysfunction HSDN C3887638 Failure to thrive in infant C0162651 Gastric outlet obstruction HSDN C0037763 Spasm C0396005 Cricopharyngeal spasm UMLS C0042798 Vision dim C0268532 Deficiency of prolidase OrphaNet|HPO|MalaCards C0030193 Sense of pain C0162832 Apc HSDN C4084784 Diarrhea C0010678 Cysticercosis HSDN C0039070 Collapse fleeting C3808145 Left ventricular noncompaction 9 MalaCards C0162834 Hyperpigmentation C0015625 Fanconi anemia MalaCards C1963252 Tremor adverse event C0042514 Tachycardia, ventricular HSDN C1950154 Insomnia homeopathic medication C0022134 Islet cell adenoma MalaCards C0042571 Vertigo subjective C0033845 Pseudotumor cerebri HSDN C0020455 Hypergammaglobulinemia C0016470 Food allergy HSDN C0022107 Fussiness C3151140 Pontocerebellar hypoplasia, type 2d MalaCards|HPO C0000737 Abdomen pain C3827868 Tachycardia by ecg finding HSDN C0031911 Pigment deposition C0004608 Background retinopathy MalaCards C4085211 Pain distress question C0040582 Trachea neoplasm HSDN C3887638 Failure to thrive in infant C0036415 Sclerema neonatorum nos HSDN C4085210 Usual severity pain C0012752 Distance discrimination HSDN C0750937 Appendicular ataxia C1836474 Spinocerebellar ataxia, autosomal recessive 7 MalaCards C1557397 Adverse event associated with pain C0038187 Starvation HSDN C3815497 Cough C0027663 Neoplasms, multiple primary HSDN C4084802 Usual severity diarrhea C0086650 Mps iii d HPO C4085211 Pain distress question C0006281 Congenital bronchogenic cyst HSDN C0020672 Body temperature decreased C0338503 Septo-optic dysplasia HSDN C0020450 Hyperemesis gravidarum C0795623 Hepatitis a vaccine, inactivated HSDN C2919142 Short stature adverse event C0265226 Hecht syndrome (disorder) OrphaNet|HPO C4084774 Have weight loss C1856243 Growth factors, combined defect of OrphaNet|MalaCards C0423714 Genitofemoral nerve neuralgia C0270891 Nerve plexus disorder, nos UMLS C0005745 Blepharoptosis C2931482 Neurofibromatosis-noonan syndrome OrphaNet|HPO|MalaCards C0151889 Reflexes tendon increased C1846564 Spastic paraplegia 7, autosomal recessive MalaCards|HPO C0026838 Spasticity muscle C2750220 Karak syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0152814 Epididymal tuberculosis MalaCards C0027796 Neuralgias C0018920 Hemangioma, cavernous HSDN C2911645 Weight loss adverse event C0001403 Addison disease OrphaNet|HSDN C0150045 Urinary incontinence urge C0406670 Burning vulva HSDN C4085862 Bothered by nausea C0205788 Histiocytoid hemangioma HSDN C0031911 Pigment deposition C0206663 Neuroectodermal tumor, primitive MalaCards C0034933 Abnormal reflexes C0032965 Pregnancy complications, infectious HSDN C0518090 Frequency of pain question C0162651 Gastric outlet obstruction HSDN C2024878 Cardiovascular surgery result: dyspnea C0003850 Arteriosclerosis HSDN C0859879 Other specified abnormality of urination C0042035 Urination disorders UMLS C1963184 Nystagmus adverse event C0376329 New variant creutzfeldt-jakob disease MalaCards C0520966 Coordination impaired C0234144 Dysgraphia UMLS C0009398 Color vision defects C3888009 Macular dystrophy, retinal, 3 MalaCards C0557874 Global developmental delay C1801950 Opitz-g syndrome, type 2 OrphaNet|HPO|MalaCards C0424755 Fever symptoms C0039231 Tachycardia HSDN C0042024 Urine incontinence C4042784 Feeding and eating disorders HSDN C4084788 Have dizziness C0038579 Substance abuse, intravenous HSDN C0015672 Decreased energy C0033860 Psoriasis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030469 Paranasal sinus diseases HSDN C0015469 Facial paralysis C0037933 Spinal diseases HSDN C0042024 Urine incontinence C0002395 Alzheimer's disease HSDN C1549543 Administration method - pain C0002438 Amebiasis HSDN C1963065 Apnea adverse event C0007820 Cerebrovascular disorders HSDN C1549543 Administration method - pain C0021832 Intestinal diseases, parasitic HSDN C1527344 Dysphonia C1720922 Respiratory aspiration HSDN C2242996 Tingling C0031028 Periapical diseases HSDN C4084724 Usual severity constipation C0206171 Community acquired infections HSDN C0476273 Distress respiratory C0748355 Acute respiratory distress UMLS C3274924 Have been coughing C0023786 Mucopolysaccharidosis i OrphaNet C0019209 Large liver C0009714 Hepatic fibrosis, congenital HPO C0036572 Convulsion C1865285 Megalencephaly cutis marmorata telangiectatica congenita HPO|UMLS C0700590 Diaphoresis excessive C1845861 Mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait HPO C0031256 Petechia C1861195 Glanzmann thrombasthenia, autosomal dominant HPO C2984058 Have pain C0080233 Tooth loss HSDN C0013395 Indigestion C0008066 Child behavior disorders HSDN C0850758 Pain pelvic C0563150 Catastrophization HSDN C2919142 Short stature adverse event C1857276 Trichohepatoenteric syndrome MalaCards|HPO C0020455 Hypergammaglobulinemia C0034735 Raynaud phenomenon HSDN C0030193 Sense of pain C3266155 Functional abdominal pain syndrome UMLS C0003862 Pain joint C0032749 Post-kala-azar dermal leishmaniasis MalaCards C0009080 Finger clubbing C1510415 Osteosclerotic myeloma MalaCards C0026826 High muscle tone C0010314 Cri-du-chat syndrome MalaCards C4084723 Constipation C0025162 Megacolon toxic HSDN C3665386 Abnormal vision C0271972 Thiamine-responsive megaloblastic anemia MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0000833 Abscess HSDN C4084768 Usual severity vomiting C0008924 Cleft lip HSDN C0003079 Pupillary inequality C0677866 Brain stem neoplasms HSDN C1963281 Vomiting adverse event C0265673 Congenital kyphosis HSDN C0557874 Global developmental delay C0035934 Rubinstein-taybi syndrome OrphaNet|MalaCards C0037316 Not enough sleeping C0038271 Stereotyped behavior HSDN C0013404 Respiratory difficulty C1963229 Retinal detachment adverse event HSDN C1557397 Adverse event associated with pain C0041601 Ulna fracture HSDN C0851578 Disorder sleep C0019693 Hiv infections HSDN C2919142 Short stature adverse event C4014954 Neutropenia, severe congenital, 6, autosomal recessive MalaCards C0030200 Intractable pain C0016053 Fibromyalgia HSDN C0518090 Frequency of pain question C0040582 Trachea neoplasm HSDN C0001825 Agraphia C0751072 Frontotemporal lobar degeneration HSDN C3887873 Hearing loss C0043168 Whooping cough due to unspecified organism HSDN C2984058 Have pain C0085632 Apathy HSDN C0242936 Center pain C0040948 Trichostrongyliasis HSDN C0184567 Pain acute C0238124 Necrotizing fasciitis HSDN C0018681 Headache, cephalalgia C1963064 Anxiety adverse event HSDN C1963167 Memory impairment adverse event C0024198 Lyme disease MalaCards C0025323 Bleeding menstrual heavy C1856448 Bernard soulier syndrome, type c HPO C0917816 Deficiency mental C2931416 Fara chlupackova syndrome OrphaNet|HPO C2242996 Tingling C0002170 Alopecia HSDN C0003862 Pain joint C0035012 Reiter syndrome OrphaNet|MalaCards C4084788 Have dizziness C0035302 Retinal artery occlusion HSDN C0015300 Ocular proptosis C0027831 Neurofibromatosis 1 OrphaNet C4084767 Bothered by vomiting C0009375 Colonic neoplasms HSDN C0019572 Hairiness C1857588 Amaurosis hypertrichosis MalaCards C0011991 Loose stools C0042514 Tachycardia, ventricular HSDN C0036572 Convulsion C0751918 Cockayne pelizaeus merzbacher disease MalaCards C2237041 Shox gene with short stature C1856899 Cutaneous albinism hermine phenotype OrphaNet|MalaCards C0042798 Vision dim C1833809 Optic atrophy and cataract, autosomal dominant HPO C1565249 Limitation, mobility C0019554 Dislocate hip HSDN C0240715 Perineal lump C0153446 Malignant neoplasm of anus UMLS C0232943 Metromenorrhagia C0008533 Hemophilia b MalaCards C4085211 Pain distress question C0162651 Gastric outlet obstruction HSDN C2911647 Weight gain adverse event C0026269 Mitral valve stenosis HSDN C2984058 Have pain C0037997 Splenic diseases HSDN C4084802 Usual severity diarrhea C0041307 Tuberculosis, bovine HSDN C0030193 Sense of pain C0017671 Glomus jugulare tumor HSDN C2024878 Cardiovascular surgery result: dyspnea C0030290 Fistula pancreatic HSDN C1263846 Attention deficit disorder with hyperactivity C0796022 Lujan fryns syndrome OrphaNet|HPO C0005904 Alteration in body temperature C1866994 Ulnar-mammary syndrome MalaCards C0000737 Abdomen pain C0037299 Skin ulcer HSDN C0349588 Stature short C2931902 Acute brachial neuritis MalaCards C3539892 Pelvic pain in front C0010695 Cystocele HSDN C0015468 Face pain C0037369 Smoking HSDN C0002962 Angina C0011649 Dermoid cyst HSDN C3539892 Pelvic pain in front C0001418 Adenocarcinoma HSDN C0030975 Disorders perception C0004364 Autoimmune diseases HSDN C2315100 Pediatric failure to thrive C3553571 Congenital disorder of glycosylation, type iik MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0206655 Alveolar rhabdomyosarcoma HSDN C0557874 Global developmental delay C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0005745 Blepharoptosis C3150708 Chromosome 16p13.3 duplication syndrome MalaCards C4084768 Usual severity vomiting C0007097 Carcinomas HSDN C1962972 Proteinuria adverse event C0010054 Coronary arteriosclerosis HSDN C0233993 Sexuality related problems C0278103 Fear of coitus UMLS C0917816 Deficiency mental C0795950 Corpus callosum agenesis neuronopathy OrphaNet|HPO|MalaCards C0151311 Cranial nerve palsy C1318518 Infantile malignant osteopetrosis MalaCards|HPO C0036659 Sensation disorder C0039984 Thoracic outlet syndrome HSDN C1963252 Tremor adverse event C0022362 Jaw diseases HSDN C2237041 Shox gene with short stature C2936859 N syndrome MalaCards C0011991 Loose stools C2749602 Autoimmune polyendocrinopathy syndrome, type i, with reversible metaphyseal dysplasia HPO C0557874 Global developmental delay C2749562 Nadh-cytochrome b5 reductase deficiency, type ii HPO C4084802 Usual severity diarrhea C1962958 Hematoma adverse event HSDN C0027796 Neuralgias C0009240 Cognition HSDN C0013404 Respiratory difficulty C0007787 Transient ischemic attack HSDN C3641756 Have diarrhea C0004782 Basal ganglia diseases HSDN C0700078 Deep tendon reflex decrease C1851708 Encephalopathy, recurrent, of childhood MalaCards C0040485 Wryneck C0796279 Carnevale syndrome MalaCards|HPO|UMLS C3641756 Have diarrhea C0002986 Fabry disease MalaCards|HPO C0750937 Appendicular ataxia C0024814 Marinesco-sjogren syndrome MalaCards|HPO C4085548 Usual severity dizziness C0026946 Mycoses HSDN C1279888 Proteinuria of undiagnosed cause C0023267 Fibroid tumor HSDN C0009806 Constipate C1707439 Colorectal mucinous adenocarcinoma UMLS C1963087 Constipation adverse event C0266209 Congenital dilatation of colon MalaCards C4085210 Usual severity pain C0344435 Ventricular fibrillation by ecg finding HSDN C4084776 Weight loss C0027947 Neutropenia HSDN C1838869 Proximal neurogenic muscle weakness C0270969 Zebra body myopathy OrphaNet C0003811 Cardiac rhythm disturbance C0175704 Leopard syndrome OrphaNet|MalaCards C0007815 Cerebrospinal fluid rhinorrhoea C0338575 Sagittal sinus thrombosis HSDN C0085602 Polydypsia C0687720 Central diabetes insipidus OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0010823 Cytomegalovirus infections HSDN C0518090 Frequency of pain question C0752130 Spinal cord ischemia HSDN C0022346 Yellow skin C0009375 Colonic neoplasms HSDN C1999266 Depression adverse event C0012236 Digeorge syndrome MalaCards C0917816 Deficiency mental C3180937 15q11.2 microdeletion MalaCards C1963093 Dizziness adverse event C0546884 Hypovolemia HSDN C0028738 Nystagmus C1856689 Friedreich ataxia 1 HPO C0007859 Pain neck C0004238 Atrial fibrillation HSDN C1963281 Vomiting adverse event C0004044 Asphyxia HSDN C0518090 Frequency of pain question C1656583 Rosacea HSDN C0020673 Hypothermia (central) (local) C0080179 Vertebra fracture HSDN C2242996 Tingling C0152180 Accessory nerve diseases HSDN C0151786 Weakness muscle C0040156 Thyrotoxicosis MalaCards C2024878 Cardiovascular surgery result: dyspnea C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4085211 Pain distress question C1546602 Specimen source codes - diverticulum HSDN C0013404 Respiratory difficulty C0029185 Orbit tumor HSDN C0019209 Large liver C0917715 Hajdu-cheney syndrome HPO C1536086 Eye numbness C0854097 Hypoesthesia eye UMLS C0015970 Fever unknown origin C0019196 Hepatitis c HSDN C4084769 Vomiting frequency C1457883 Aggressive reaction HSDN C1549543 Administration method - pain C0043251 Wounds and injuries HSDN C2984058 Have pain C0027086 Myoma HSDN C2911645 Weight loss adverse event C0004623 Bacterial infections HSDN C0042963 Symptoms vomiting C0026848 Myopathy HSDN C4085317 Diarrhea frequency C0085389 Bacillaceae infection HSDN C1963086 Confusion adverse event C0751865 Alcohol-induced disorders, nervous system HSDN C0030193 Sense of pain C0037019 Shy-drager syndrome HSDN C0751188 Dural headache post puncture C0475524 Headache; spinal and epidural anesthesia-induced, postpartum, puerperal UMLS C0518090 Frequency of pain question C0038034 Beurmann disease HSDN C0150055 Pain chronic C0599412 Lordosis [mating posture] HSDN C0429002 Aberrantly conducted complex C0264886 Conduction disorder of the heart UMLS C3274924 Have been coughing C1704272 Benign prostatic hyperplasia HSDN C0040822 D tremors C0042847 Vitamin b 12 deficiency HSDN C0018772 Deafness C0268250 Gaucher disease, type 2 (disorder) MalaCards C0031911 Pigment deposition C0030297 Pancreatic neoplasm MalaCards C1279888 Proteinuria of undiagnosed cause C4042866 Acute symptom flare HSDN C2024893 Cardiovascular surgery result: fatigue C2586211 Thrombosis of blood vessel HSDN C0019521 Hiccoughs C0030567 Parkinson disease HSDN C0040460 Dental pain C0428953 Ecg infarction myocardial HSDN C0019079 Bloody sputum C1336111 Stage ia adenosquamous cell carcinoma of lung UMLS C0020673 Hypothermia (central) (local) C0009241 Cognition disorders HSDN C4084784 Diarrhea C0004692 Balantidiasis HSDN C3463815 Feel fatigue C2937421 Prostatic hyperplasia HSDN C0037763 Spasm C0040034 Thrombocytopenia HSDN C0460137 Push down or depress C2931082 Familial apoceruloplasmin deficiency MalaCards C0042024 Urine incontinence C1705812 Nci thesaurus role HSDN C0150055 Pain chronic C0314657 Genetic predisposition HSDN C0011991 Loose stools C0585442 Osteosarcoma of bone HSDN C0003469 Anxiety disorder C1847987 Huntington disease-like 2 MalaCards|HPO C0010200 Cough symptom C0032310 Pneumonia, viral HSDN C0151889 Reflexes tendon increased C2931356 Spastic paraplegia type 5a, recessive MalaCards C0022346 Yellow skin C0037933 Spinal diseases HSDN C0085636 Light sensitivity C0079504 Hermanski-pudlak syndrome OrphaNet|HSDN|MalaCards C1519353 Skin eruption papular C0024525 Malacoplakia MalaCards C0151786 Weakness muscle C0282492 Sneddon syndrome OrphaNet|HPO|MalaCards C0012833 Dizzy C0020615 Hypoglycemia UMLS C0042571 Vertigo subjective C0039263 Takayasu arteritis HSDN C0036659 Sensation disorder C1263846 Attention deficit hyperactivity disorder HSDN C0013390 Cramps menstrual C1962979 Burn adverse event HSDN C0030193 Sense of pain C0014179 Endometritis HSDN C0000737 Abdomen pain C0039504 Injuries tendon HSDN C1962972 Proteinuria adverse event C0006818 Campylobacter infection HSDN C1961131 Cough adverse event C0243025 Hantavirus pulmonary syndrome MalaCards C4084766 Vomiting C0033845 Pseudotumor cerebri HSDN C2024893 Cardiovascular surgery result: fatigue C0948089 Acute coronary syndrome HSDN C3641756 Have diarrhea C0024620 Primary malignant neoplasm of liver MalaCards C0424755 Fever symptoms C0025286 Meningioma HSDN C1963091 Diarrhea adverse event C0033906 Psychological theories HSDN C2919142 Short stature adverse event C0033806 Pseudohypoparathyroidism HPO C0542476 Forgetful C2931082 Familial apoceruloplasmin deficiency MalaCards C0557874 Global developmental delay C3891556 Chromosome xq26.3 duplication syndrome MalaCards C0020578 Hyperventilate C0155877 Allergic asthma DiseaseOntology C3539893 Pelvic pain occurs with intercourse C0035358 Retroperitoneal neoplasm HSDN C0027498 Nausea vomiting C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C4085210 Usual severity pain C0030636 Pasteurella infection HSDN C0037317 Sleep disturbance C0338497 Reversed sleep wake cycle UMLS C0036572 Convulsion C0040336 Tobacco use disorder HSDN C3641755 Have constipation C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C1557397 Adverse event associated with pain C0149721 Left ventricular hypertrophy HSDN C4085222 Nausea C0023343 Leprosy HSDN C0039870 Leanness C3541306 Plasmodium measurement HSDN C4084775 Usual severity weight loss C0032533 Polymyalgia rheumatica MalaCards C0018524 Hallucinate C0268569 Intermittent maple syrup urine disease HPO C0278107 Ejaculation pain C0017412 Genital diseases, male UMLS C0547030 Sensory perceptual alteration: visual C3648257 Late effects of nontraumatic intracerebral hemorrhage vision disturbances UMLS C0036396 Sciatica C0042376 Vascular headaches HSDN C2984058 Have pain C0206663 Neuroectodermal tumor, primitive HSDN C3463815 Feel fatigue C0023448 Lymphoid leukemia HSDN C0742665 Colon rectal pain C0742648 Colon rectal fissure UMLS C0015970 Fever unknown origin C0162872 Aortic aneurysm, thoracic HSDN C1961131 Cough adverse event C0085092 Parenting behavior HSDN C0002962 Angina C0023896 Alcoholic liver diseases HSDN C4084766 Vomiting C0085423 Gram-negative bacterial infections HSDN C4084769 Vomiting frequency C2240374 Eosinophil count raised HSDN C1557397 Adverse event associated with pain C0027726 Nephrotic syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0001144 Acne vulgaris HSDN C3829611 Nausea frequency C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C2315100 Pediatric failure to thrive C0917715 Hajdu-cheney syndrome MalaCards|HPO C0020673 Hypothermia (central) (local) C0034040 Puerperal disorders HSDN C3898969 Have been vomiting C0017160 Gastroenteritis DiseaseOntology C0026821 Cramp C0270857 Epilepsy, reflex HSDN C1069915 Vertigo C0031350 Pharyngitis HSDN C0027497 Queasy C1706377 Memory device component HSDN C0023530 Leukopenia C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0042830 Perception visual HSDN C0030552 Paralysis partial C1849322 Sandhoff disease, infantile type HPO C0013604 Edematous C0013238 Dry eye syndromes HSDN C2096293 Ent surgical result ear vertigo C2674766 Myokymia 1 HPO C0042940 Disorder of voice C0033578 Prostatic neoplasms HSDN C0013132 Drooling C3151056 Spastic paraplegia 51, autosomal recessive MalaCards|HPO C0036396 Sciatica C1837218 Cleft palate, isolated HSDN C2203646 Jaundice C0002874 Aplastic anemia HSDN C4085548 Usual severity dizziness C0020179 Huntington disease HSDN C0004093 Asthenia C0032087 Plant poisoning HSDN C4085862 Bothered by nausea C0035242 Respiratory tract diseases HSDN C0700072 Encounter due to stillbirth C2673477 Hypophosphatasia, perinatal lethal HPO C0020672 Body temperature decreased C1762616 Meningioma, benign, no icd-o subtype HSDN C2242996 Tingling C0023895 Liver diseases HSDN C0270948 Neurogenic muscular atrophy C1876175 Ataxia-telangiectasia variant MalaCards C0240735 Personality change C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C0019079 Bloody sputum C0747260 Paratracheal mass UMLS C3463815 Feel fatigue C0405580 Adrenal cortical hypofunction HSDN C4085222 Nausea C0007222 Cardiovascular diseases HSDN C0018681 Headache, cephalalgia C2979888 Fever, australian q MalaCards C1546759 Specimen source codes - pustule C0272295 Purpura, rheumatica MalaCards C0006370 Bulimia C0040428 Abrasion dental HSDN C0042940 Disorder of voice C0018199 Granuloma, plasma cell HSDN C3898969 Have been vomiting C0079631 Interdisciplinary communication HSDN C0009398 Color vision defects C0086543 Cataract nos HSDN C0041657 Consciousness loss C0040127 Thyroid crisis HSDN C0232503 Bleeding umbilical C0473789 Umbilical hemorrhage after birth nos UMLS C1384666 Decreased hearing C1853473 Paget disease of bone 4 MalaCards C3887638 Failure to thrive in infant C1854630 Growth deficiency and mental retardation with facial dysmorphism MalaCards|HPO C3539893 Pelvic pain occurs with intercourse C1299262 Sarcoma - category (morphologic abnormality) HSDN C3665386 Abnormal vision C1837073 Spondylometaphyseal dysplasia with cone-rod dystrophy OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0009241 Cognition disorders HSDN C1963093 Dizziness adverse event C4050613 Anxiety scale (basc-2) HSDN C0518090 Frequency of pain question C0041318 Tuberculosis, meningeal HSDN C2203646 Jaundice C0272118 Warm autoimmune hemolytic anemia MalaCards C0010200 Cough symptom C0027726 Nephrotic syndrome HSDN C2237041 Shox gene with short stature C2931648 Larsen syndrome, dominant type MalaCards|HPO C0424755 Fever symptoms C0027345 Nairobi sheep disease HSDN C0042798 Vision dim C1844671 Dermoids of cornea OrphaNet|MalaCards C4084726 Distress cough C0019196 Hepatitis c HSDN C0518090 Frequency of pain question C1522137 Hypertriglyceridemia result HSDN C3665347 Vision impaired C3502492 Microcephaly with chorioretinopathy, autosomal recessive OrphaNet|HPO|MalaCards C0030975 Disorders perception C1839259 Bulbo-spinal atrophy, x-linked HSDN C0043094 Weight gain C0040558 Toxoplasmosis HSDN C0013604 Edematous C0032965 Pregnancy complications, infectious HSDN C0022346 Yellow skin C3273134 Extrahepatic bile duct cystadenocarcinoma UMLS C0349588 Stature short C1859305 Cerebellar ataxia and hypogonadotropic hypogonadism HPO C0018681 Headache, cephalalgia C0010692 Cystitis HSDN C0030193 Sense of pain C0032780 Postmortem changes HSDN C2984058 Have pain C0039263 Takayasu arteritis HSDN C1145670 Failure respiratory C0268360 Osteogenesis imperfecta, recessive perinatal lethal HPO C4084724 Usual severity constipation C0001580 Adolescent behavior HSDN C1963281 Vomiting adverse event C0023895 Liver diseases HSDN C0518090 Frequency of pain question C0014100 Endarteritis, nos HSDN C0007758 Cerebellar ataxia C0007134 Renal cell carcinoma HSDN C0023222 Lower extremity pain musculoskeletal C0028250 Lower extremity cramp nocturnal UMLS C0242936 Center pain C0007273 Carotid artery diseases HSDN C4085548 Usual severity dizziness C0040128 Thyroid diseases HSDN C0025287 Meningitis-like C0007361 Cat-scratch disease HSDN C0041667 Low weight C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C0857305 Thrombocytopenia purpura C0040100 Thymoma HSDN C4084776 Weight loss C0024894 Mastitis HSDN C1836296 Lower extremity weakness C1853926 Nonaka myopathy OrphaNet|MalaCards C1963184 Nystagmus adverse event C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C4085222 Nausea C0028738 Nystagmus HSDN C1510417 Apraxia of gait C0015806 Femur neck fracture HSDN C0020578 Hyperventilate C1706377 Memory device component HSDN C3887638 Failure to thrive in infant C1865596 Desmosterolosis MalaCards|HPO C0013404 Respiratory difficulty C1720777 Functional laterality HSDN C0413252 Hypothermia due to exposure C0042075 Urologic diseases HSDN C0595939 Stillborn C1842704 Gaucher disease, perinatal lethal OrphaNet|HPO|MalaCards C2107742 Confusion constant C0221560 Chronic confusion UMLS C2024893 Cardiovascular surgery result: fatigue C0025202 Melanoma HSDN C0036572 Convulsion C2750791 Mental retardation, autosomal recessive 13 HPO C0028738 Nystagmus C1842362 Hermansky-pudlak syndrome 2 MalaCards|HPO C4084802 Usual severity diarrhea C0358297 Anthrax vaccines HSDN C0018681 Headache, cephalalgia C1706728 Adrenal gland composite pheochromocytoma UMLS C0424755 Fever symptoms C0037305 Neoplasm, skull HSDN C1963137 Hydrocephalus adverse event C0795825 Chromosome 8, trisomy 8p MalaCards C1963281 Vomiting adverse event C0004161 Athletic injuries HSDN C0004093 Asthenia C0029191 Orchitis HSDN C1962972 Proteinuria adverse event C0013922 Embolism HSDN C1963137 Hydrocephalus adverse event C2931282 Skeletal dysplasia, san diego type MalaCards|HPO C0028738 Nystagmus C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0030552 Paralysis partial C0011881 Diabetic nephropathy HSDN C4084802 Usual severity diarrhea C0033906 Psychological theories HSDN C4084774 Have weight loss C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C0344315 Mood depressed C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C2984057 Have nausea C0342443 Adrenal cushing's syndrome HSDN C0413252 Hypothermia due to exposure C0035126 Reperfusion injury HSDN C0746674 Muscle weakness generalized C1855849 Bartter syndrome, antenatal , type 2 HPO C0263534 Beau's line C0221260 Dystrophia unguium UMLS C2315100 Pediatric failure to thrive C1856302 Gsd iv, nonprogressive hepatic HPO C0013421 Dystonia C0751267 Encephalopathy, subacute necrotizing, infantile MalaCards C0029163 Hemorrhage mouth C0040443 Avulsed tooth HSDN C0011206 Delirium acute C0015745 Ingestive behavior HSDN C0005745 Blepharoptosis C1956391 Temporal arteritis MalaCards|HPO C0278230 Retinal sign, nos C0035309 Retinal diseases UMLS C4084776 Weight loss C0276275 Disease due to parvoviridae HSDN C0518090 Frequency of pain question C0018946 Hematoma, subdural HSDN C0030552 Paralysis partial C1423541 Vangl2 gene HSDN C4084802 Usual severity diarrhea C0043528 Zoonoses HSDN C0349588 Stature short C1442965 Avascular necrosis of the capital femoral epiphysis MalaCards C0424755 Fever symptoms C0007932 Chagas' disease + no organ inv DiseaseOntology|MalaCards C4084767 Bothered by vomiting C0042035 Urination disorders HSDN C1963091 Diarrhea adverse event C0027794 Neural tube defects HSDN C4042891 Sleep wake disorders C0036439 Scoliosis, unspecified HSDN C1557397 Adverse event associated with pain C0028064 Niemann-pick diseases HSDN C0557874 Global developmental delay C0268680 Biotin deficiency MalaCards C0000737 Abdomen pain C0029458 Osteoporosis, postmenopausal HSDN C3829611 Nausea frequency C0004238 Atrial fibrillation HSDN C0497406 Over weight C0079744 Diffuse large b-cell lymphoma HSDN C1963071 Back pain adverse event C0007134 Renal cell carcinoma HSDN C1384666 Decreased hearing C1956391 Temporal arteritis MalaCards C0426579 Anorexia symptom C1721053 Female athlete triad HSDN C0085632 Listlessness C0860660 La belle indifference UMLS C4085548 Usual severity dizziness C0042170 Uveomeningoencephalitic syndrome HSDN C4085862 Bothered by nausea C0007760 Cerebellar diseases HSDN C3641756 Have diarrhea C0016045 Fibroma HSDN C3539895 Pelvic pain occurs with bowel movement C0035358 Retroperitoneal neoplasm HSDN C0030486 Extremity paralysis, lower C0024141 Lupus erythematosus, systemic HSDN C0012833 Dizzy C4049994 Insulin resistance measurement HSDN C3539020 Pelvic pain decreasing in frequency C1881674 Medical device emits smoke HSDN C0033377 Caudal displacement C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C1557397 Adverse event associated with pain C0004030 Aspergillosis HSDN C0026838 Spasticity muscle C0015519 Factor x deficiency HSDN C0424755 Fever symptoms C1963164 Lymphopenia adverse event HSDN C0015468 Face pain C0033578 Prostatic neoplasms HSDN C0231218 Malaise generalized C3899980 Bclc stage b adult hepatocellular carcinoma UMLS C0747556 Pharyngitis recurrent C0015773 Felty syndrome OrphaNet|MalaCards C0349506 Sun sensitivity C0406557 Poikiloderma of kindler OrphaNet|HPO|MalaCards C0013421 Dystonia C3539013 Aicardi-goutieres syndrome 6 MalaCards C0015469 Facial paralysis C0015414 Eye neoplasms HSDN C1557397 Adverse event associated with pain C0038862 Inflammation purulent HSDN C0020672 Body temperature decreased C0017181 Gastrointestinal hemorrhage HSDN C0038868 Supranuclear palsy progressive C0011263 Multi-infarct dementia HSDN C3829611 Nausea frequency C0037929 Spinal cord injuries HSDN C0028738 Nystagmus C1846790 Joubert syndrome 4 (disorder) MalaCards|HPO C3887638 Failure to thrive in infant C0079583 Ichthyosiform erythroderma, congenital MalaCards C4084802 Usual severity diarrhea C0043325 Xanthomatosis HSDN C0020458 Hyperhydrosis C1851480 Greither disease OrphaNet C0042755 Virilisation C0028949 Oligomenorrhea HSDN C1279888 Proteinuria of undiagnosed cause C3665770 Acquired lipoatrophic diabetes MalaCards C0006370 Bulimia C0039336 Gustatory sense HSDN C0041105 Jaw spasm C0079943 Oral fistulas HSDN C2024893 Cardiovascular surgery result: fatigue C0279606 Childhood hepatocellular carcinoma MalaCards C3641756 Have diarrhea C0014556 Epilepsy, temporal lobe HSDN C0009792 Consciousness disorder C0041327 Tuberculosis, pulmonary HSDN C0522224 Palsied C0236736 Cocaine-related disorders HSDN C4085317 Diarrhea frequency C0027858 Neuroma HSDN C0002962 Angina C0040921 Trichomonas infections HSDN C0151311 Cranial nerve palsy C1306794 Wound botulism OrphaNet|MalaCards C0038990 Sweats C0023931 Lobstein's disease OrphaNet C0011991 Loose stools C0221036 Acrodermatitis enteropathica HPO|UMLS C0242936 Center pain C0009353 Colles' fracture HSDN C0518090 Frequency of pain question C0006264 Bronchial neoplasms HSDN C0014591 Bleeding nose C1264040 Von willebrand disease, type 2 HPO C0015799 Feminisation C0237873 Physiological sexual disorders HSDN C0013604 Edematous C0206138 Crest syndrome OrphaNet|MalaCards C0040034 Thrombocytopenia C0043207 Wolfram syndrome HPO C1279888 Proteinuria of undiagnosed cause C0000833 Abscess HSDN C0036572 Convulsion C0015745 Ingestive behavior HSDN C3665347 Vision impaired C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C1963184 Nystagmus adverse event C2751843 Leukoencephalopathy, cystic, without megalencephaly MalaCards|HPO C0018681 Headache, cephalalgia C0015732 Fecal incontinence HSDN C0007814 Cerebrospinal fluid otorrhea C0206717 Olfactory neuroblastoma HSDN C0557874 Global developmental delay C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C0221752 Rbc urine C1832949 Infundibulopelvic dysgenesis MalaCards C0020903 Illusion C1962986 Glaucoma adverse event HSDN C3641756 Have diarrhea C0022593 Keratosis HSDN C2024893 Cardiovascular surgery result: fatigue C0062527 Hepatitis b vaccine HSDN C0242936 Center pain C0085426 Gram-positive bacterial infections HSDN C0018772 Deafness C0015393 Eye abnormalities MalaCards|HSDN C0522224 Palsied C0027708 Nephroblastoma HSDN C0013404 Respiratory difficulty C4225400 Interstitial lung and liver disease UMLS C0460137 Push down or depress C0687720 Central diabetes insipidus OrphaNet|MalaCards C1963065 Apnea adverse event C1548578 Location characteristic id - smoking HSDN C0002962 Angina C0014854 Esophageal diverticulum HSDN C0037316 Not enough sleeping C2984299 Asthma pathway HSDN C3887638 Failure to thrive in infant C1855100 Methylmalonyl-coa epimerase deficiency MalaCards|HPO C0018926 Emesis bloody C2984289 Melanoma pathway HSDN C0013395 Indigestion C0023055 Laryngeal neoplasm HSDN C2911645 Weight loss adverse event C0036341 Schizophrenia HSDN C0035229 Respiratory function impaired C3810384 Nemaline myopathy 9 MalaCards C0277959 Hair coarseness C1860238 Woolly hair, autosomal dominant HPO C0151786 Weakness muscle C0039483 Giant cell arteritis MalaCards|HPO C4085862 Bothered by nausea C0022336 Creutzfeldt-jakob disease HSDN C4085222 Nausea C0035412 Rhabdomyosarcoma HSDN C1069915 Vertigo C0027765 Nervous system disorder HSDN C0018808 Murmur C2239176 Liver carcinoma HSDN C0004134 Dyssynergia C0032344 Poisoning aspects HSDN C0015230 Exanthem C0570211 Insulin adverse reaction humulin UMLS C3539896 Pelvic pain occurs with urination C0032966 Complication, neoplastic pregnancy HSDN C0851578 Disorder sleep C0027627 Neoplasm metastasis HSDN C0033377 Caudal displacement C1863371 Blepharophimosis, epicanthus inversus, and ptosis 3, formerly HPO C0020305 Fetal edema C0265282 Fibrochondrogenesis HPO C1279888 Proteinuria of undiagnosed cause C0018621 Hay fever HSDN C1510417 Apraxia of gait C0338451 Frontotemporal dementia HSDN C0751401 Ophthalmoparesis C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0349588 Stature short C1970414 Osteogenesis imperfecta, type v MalaCards|HPO C0349588 Stature short C2931894 Mucolipidosis 2 OrphaNet|HPO|MalaCards C0812426 Kidney problem C0743163 Dialysis capd infection UMLS C2315100 Pediatric failure to thrive C1857550 11-beta-hydroxysteroid dehydrogenase, type ii HPO C0015672 Decreased energy C0015423 Eyelid diseases HSDN C2107732 Consistent heat intolerance C1862871 Anhidrosis, isolated, with normal sweat glands HPO C0035232 Diaphragmatic paralysis C0268322 Chester-type porphyria HPO C0035078 Failure kidney C0268374 Adult junctional epidermolysis bullosa (disorder) MalaCards C1549543 Administration method - pain C4041080 Neurocognitive disorders HSDN C0010520 Skin cyanosis C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0031911 Pigment deposition C0035309 Retinal diseases MalaCards C0542476 Forgetful C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C0005745 Blepharoptosis C1864668 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4 MalaCards|HPO C0042928 Paralysis vocal cord C2984291 Glioblastoma multiforme pathway HSDN C0426579 Anorexia symptom C0040053 Thrombosis HSDN C1279888 Proteinuria of undiagnosed cause C4049994 Insulin resistance measurement HSDN C0750325 Vomit recurrent C0268543 Hyperammonemia, type iii MalaCards|UMLS C2108109 Continuous electrocardiogram sinus tachycardia C0334419 Pheochromocytoma, malignant MalaCards C0018772 Deafness C3827868 Tachycardia by ecg finding HSDN C4084766 Vomiting C0014121 Bacterial endocarditis HSDN C0011991 Loose stools C0020452 Hyperemia HSDN C0027796 Neuralgias C0032343 Poisoning HSDN C0344434 Atrial fibrillation ecg C3554194 Chtd3 MalaCards C0020649 Blood pressure decreased C0345904 Malignant neoplasm of liver MalaCards C2024878 Cardiovascular surgery result: dyspnea C0022650 Kidney calculi HSDN C0262527 Intermittent abdominal pain C1970712 Multiple endocrine neoplasia, type iv OrphaNet|HPO|MalaCards C0221232 Welts C0406613 Site-specific disorder of skin UMLS C4085211 Pain distress question C0024692 Mandible fracture HSDN C0742310 Chest pain site retrosternal C0002965 Angina, unstable UMLS C0000737 Abdomen pain C0038661 Suicide HSDN C0040034 Thrombocytopenia C0206743 Rhabdoid tumor MalaCards C4084788 Have dizziness C0024530 Malaria HSDN C2242996 Tingling C0001807 Aggressive behavior HSDN C3641755 Have constipation C1546533 Specimen source codes - abscess HSDN C1963086 Confusion adverse event C0020517 Hypersensitivity HSDN C0018524 Hallucinate C0025521 Inborn errors of metabolism HSDN C3887784 Decreased urine output C4085311 Depression - recess HSDN C4084788 Have dizziness C0002438 Amebiasis HSDN C0009806 Constipate C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084723 Constipation C0014849 Esophageal and gastric varices HSDN C2919142 Short stature adverse event C1832661 Anophthalmia and pulmonary hypoplasia MalaCards|HPO C0005745 Blepharoptosis C2931705 Chromosome 15, distal trisomy 15q OrphaNet|MalaCards C0030554 Abnormal sensation C0022972 Lambert-eaton myasthenic syndrome HSDN C0005779 Clotting C2931808 Chromosome 13 ring MalaCards C4084769 Vomiting frequency C0030319 Panic disorder HSDN C0015672 Decreased energy C3850024 Transcranial direct current stimulation HSDN C0349588 Stature short C2676727 Chromosome 1q43 q44 deletion syndrome HPO C0015469 Facial paralysis C0001584 Adolescent psychology HSDN C0009460 Communication impairment C4041080 Neurocognitive disorders HSDN C0035232 Diaphragmatic paralysis C0025063 Mediastinal neoplasms HSDN C1963071 Back pain adverse event C0014848 Esophageal achalasia HSDN C1963137 Hydrocephalus adverse event C0010276 Craniopharyngioma MalaCards|HPO C3463815 Feel fatigue C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0242936 Center pain C3203360 Suppuration HSDN C0036572 Convulsion C0280788 Anaplastic ependymoma UMLS C3898969 Have been vomiting C2945560 Hemolytic HSDN C4084766 Vomiting C0025160 Megacolon HSDN C1963137 Hydrocephalus adverse event C3554246 Focal facial dermal dysplasia 4 MalaCards C0018784 Deafness sensorineural C0040046 Thrombophlebitis HSDN C0518090 Frequency of pain question C0003493 Aortic diseases HSDN C0151786 Weakness muscle C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C4084766 Vomiting C2931002 Congenital disorder of glycosylation type 1h MalaCards C0042928 Paralysis vocal cord C0007097 Carcinomas HSDN C0221752 Rbc urine C1866552 Paragangliomas 2 (disorder) MalaCards C0000727 Abdomen acute C0008519 Ectopic tissue HSDN C0010200 Cough symptom C1962986 Glaucoma adverse event HSDN C3539891 Pelvic pain to the rear C0006663 Calcinosis HSDN C4085211 Pain distress question C0039336 Gustatory sense HSDN C3463815 Feel fatigue C1962976 Ventricular fibrillation adverse event HSDN C0232461 Increased appetite C1857844 Williams-beuren region duplication syndrome MalaCards C1963091 Diarrhea adverse event C0025063 Mediastinal neoplasms HSDN C0015469 Facial paralysis C0752160 Hemangioma, cavernous, central nervous system HSDN C0018772 Deafness C1859329 Cardioauditory syndrome of sanchez cascos MalaCards C0007859 Pain neck C0016548 Foreign body migration HSDN C0035232 Diaphragmatic paralysis C0007097 Carcinomas HSDN C1279888 Proteinuria of undiagnosed cause C0431693 Renal cysts and diabetes syndrome MalaCards|HPO C1963249 Tinnitus adverse event C0521542 Brainstem infarct HSDN C0040822 D tremors C0037286 Skin neoplasms HSDN C4084769 Vomiting frequency C0037036 Sialorrhea HSDN C0030193 Sense of pain C0030215 Palate tumor HSDN C0745880 Lower extremity paresthesia numbness C0745881 Lower extremity paresthesia tingling UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0032371 Poliomyelitis HSDN C3887638 Failure to thrive in infant C2984299 Asthma pathway HSDN C0917816 Deficiency mental C3809278 Epileptic encephalopathy, childhood-onset MalaCards C0019825 Voice hoarseness C1336144 Stage ib small cell carcinoma of lung UMLS C3665492 Pigmentations C0266209 Congenital dilatation of colon MalaCards C0878773 Bladder hyperactive C0040365 Toilet training HSDN C4085210 Usual severity pain C0024286 Lymphogranuloma venereum HSDN C3641756 Have diarrhea C1865145 Congenital disorder of glycosylation type 1b MalaCards|HPO C0562483 Cough persistent C0740767 Resp_tract problem UMLS C1962972 Proteinuria adverse event C0027149 Myxoma HSDN C3274924 Have been coughing C0023343 Leprosy HSDN C0423773 Skin scaly C0079153 Hyperkeratosis, epidermolytic MalaCards|UMLS C0027066 Myoclonic jerking C0152025 Polyneuropathy HSDN C4084784 Diarrhea C0021400 Influenza HSDN C4085661 Usual severity nausea C0043065 Water electrolyte imbalance HSDN C0018681 Headache, cephalalgia C0002989 Epithelioid hemangioma of skin HSDN C0424755 Fever symptoms C0087130 Uncertain HSDN C1959630 Eye pain adverse event C1962986 Glaucoma adverse event HSDN C0564821 Arm pain right C0810058 Other connective tissue disease UMLS C0012569 Double vision C0016659 Close fracture HSDN C2315100 Pediatric failure to thrive C0266015 Congenital digestive system anomalies HSDN C2984058 Have pain C0036202 Sarcoidosis HSDN C0033377 Caudal displacement C1623209 Okihiro syndrome MalaCards C0018784 Deafness sensorineural C0268151 Classical galactosemia MalaCards C0011991 Loose stools C0023267 Fibroid tumor HSDN C0036572 Convulsion C1263960 Diabetic coma HSDN C0036572 Convulsion C1843512 Brain small vessel disease with hemorrhage MalaCards|HPO C3815497 Cough C0151636 Premature ventricular contractions HSDN C1768507 Yellow nails C0334044 Dysplasia UMLS C0751265 Learning disability C0033788 Pseudo-hurler polydystrophy MalaCards C0015672 Decreased energy C0029927 Ovarian cysts HSDN C2984057 Have nausea C0009404 Colorectal neoplasms HSDN C0011206 Delirium acute C0270611 Brain damage HSDN C0005745 Blepharoptosis C0015458 Facial hemiatrophy MalaCards C0004134 Dyssynergia C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C0497406 Over weight C0043251 Wounds and injuries HSDN C3641756 Have diarrhea C0043398 Yellow fever, urban MalaCards C0027066 Myoclonic jerking C0085078 Lysosomal storage diseases HSDN C1557397 Adverse event associated with pain C0013592 Ectropion HSDN C3641756 Have diarrhea C0014121 Bacterial endocarditis HSDN C1962972 Proteinuria adverse event C1134719 Invasive ductal breast carcinoma HSDN C4084784 Diarrhea C0029463 Osteosarcoma HSDN C0027497 Queasy C0032460 Polycystic ovary syndrome HSDN C2315100 Pediatric failure to thrive C1970173 Acyl-coa dehydrogenase family, member 9, deficiency of MalaCards C4084767 Bothered by vomiting C0042345 Varicosity HSDN C0018681 Headache, cephalalgia C0002895 Anemia, sickle cell UMLS C4084784 Diarrhea C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C3541349 Syncope C0016470 Food allergy HSDN C4084769 Vomiting frequency C0013514 Echinostomiasis DiseaseOntology C4084776 Weight loss C1998602 Meals HSDN C0043094 Weight gain C0017162 Gastroenteritis, transmissible, of swine HSDN C3641756 Have diarrhea C0085178 Needle stick injury HSDN C1963071 Back pain adverse event C0023343 Leprosy HSDN C0018991 Paralysis one side of body C0020676 Hypothyroidism HSDN C0038990 Sweats C0021670 Insulinoma OrphaNet|HPO|MalaCards C0004941 Behavioral symptoms C0751122 Infantile severe myoclonic epilepsy OrphaNet|HPO C0002962 Angina C0026946 Mycoses HSDN C0013362 Dysarthrias C0087012 Ataxia, spinocerebellar MalaCards C1263846 Attention deficit disorder with hyperactivity C0265499 49,xxxxy chromosomal anomaly OrphaNet|MalaCards C3463815 Feel fatigue C0023788 Whipple disease OrphaNet|MalaCards C0011168 Disorder deglutition C0015708 Fazio londe syndrome MalaCards|HPO C4085211 Pain distress question C3463897 Hydatidiform mole, recurrent, 1 HSDN C1963167 Memory impairment adverse event C0752235 Lyme neuroborreliosis MalaCards C0234979 Dysdiadochokinesia C1845028 Anemia, sideroblastic, and spinocerebellar ataxia HPO|UMLS C4084774 Have weight loss C0040185 Tibia fracture HSDN C0003862 Pain joint C1836122 Sarcoidosis, early-onset MalaCards C0009763 Conjunctiva inflammation C2752147 Xeroderma pigmentosum, complementation group c HPO C0002962 Angina C0039483 Giant cell arteritis HSDN C0242936 Center pain C0158329 Stenosing tenosynovitis HSDN C0023012 Delay language C0035934 Rubinstein-taybi syndrome HPO C0424755 Fever symptoms C0013922 Embolism HSDN C0151603 Edema generalized C0543697 Mixed cryoglobulinemia MalaCards C0041834 Erythematous condition C0016395 Focal dermal hypoplasia OrphaNet|HPO|MalaCards C1145670 Failure respiratory C2931282 Skeletal dysplasia, san diego type OrphaNet|HPO|MalaCards C0002962 Angina C1546533 Specimen source codes - abscess HSDN C2315100 Pediatric failure to thrive C0497552 Congenital neurologic anomalies HSDN C0013395 Indigestion C0010823 Cytomegalovirus infections HSDN C2984057 Have nausea C0043065 Water electrolyte imbalance HSDN C0026838 Spasticity muscle C0022650 Kidney calculi HSDN C0018681 Headache, cephalalgia C0039590 Testicular neoplasms HSDN C0042963 Symptoms vomiting C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C2984058 Have pain C0004031 Aspergillosis, allergic bronchopulmonary HSDN C0015970 Fever unknown origin C0036202 Sarcoidosis HSDN C1963071 Back pain adverse event C1090821 Sepsis (invertebrate) HSDN C4084784 Diarrhea C1550639 Specimen type - fistula HSDN C0018991 Paralysis one side of body C0016169 Pathologic fistula HSDN C0030193 Sense of pain C0018023 Nodular goiter HSDN C4084768 Usual severity vomiting C0276386 Mosquito-borne viral fever, oropouche MalaCards C3539022 Pelvic pain decreasing in severity C0026769 Multiple sclerosis HSDN C1384666 Decreased hearing C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards|HPO C0026821 Cramp C0034882 Rectal diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0038041 Spotted fevers DiseaseOntology|MalaCards C2984058 Have pain C0019342 Genital herpes HSDN C2984058 Have pain C0038579 Substance abuse, intravenous HSDN C0020673 Hypothermia (central) (local) C0032371 Poliomyelitis HSDN C3146279 Coma C1720777 Functional laterality HSDN C0023380 Lethargy C0749420 Thyroid agenesis HPO C0027497 Queasy C0521607 Peritoneal fibrosis HSDN C0019572 Hairiness C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C1963091 Diarrhea adverse event C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C0018772 Deafness C1556061 Electric injuries HSDN C0085602 Polydypsia C0037421 Social isolation HSDN C1384666 Decreased hearing C0016395 Focal dermal hypoplasia OrphaNet|HPO|MalaCards C0020580 Decreased sensation C0041330 Tuberculosis, spinal HSDN C0007859 Pain neck C0038017 Congenital spondylolisthesis HSDN C3641755 Have constipation C0004238 Atrial fibrillation HSDN C3887873 Hearing loss C1834711 Cerebelloparenchymal disorder vi MalaCards C0426579 Anorexia symptom C0004096 Asthma HSDN C0917816 Deficiency mental C0265211 Marshall-smith syndrome MalaCards|HPO C0019825 Voice hoarseness C0034088 Pulmonary valve insufficiency HSDN C4085211 Pain distress question C0267941 Pancreatitis, acute necrotizing HSDN C3539896 Pelvic pain occurs with urination C0005690 Bladder fistula HSDN C1963093 Dizziness adverse event C0149721 Left ventricular hypertrophy HSDN C0011991 Loose stools C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0233794 Memory impaired C2986550 Pituicytoma MalaCards C2024893 Cardiovascular surgery result: fatigue C0001173 Adult pyloric stenosis HSDN C1279888 Proteinuria of undiagnosed cause C0027765 Nervous system disorder HSDN C0036396 Sciatica C0585051 Acute sciatica UMLS C0557874 Global developmental delay C1842563 Heterotopia, periventricular, autosomal recessive HPO C0034150 Skin purpura C0031069 Familial mediterranean fever HSDN C0015970 Fever unknown origin C0001621 Adrenal gland diseases HSDN C3641756 Have diarrhea C0085073 Prosthesis-related infection HSDN C0233514 Behavior abnormal C3280479 Pitt-hopkins-like syndrome 2 MalaCards C0022346 Yellow skin C0018081 Gonorrhea HSDN C4084727 Cough frequency C0011981 Diaphragmatic eventration HSDN C1963071 Back pain adverse event C0334299 Carcinoid tumor no icd-o subtype HSDN C0026838 Spasticity muscle C0022716 Menkes kinky hair syndrome OrphaNet|HPO|MalaCards C0010200 Cough symptom C0524909 Hepatitis b, chronic HSDN C2317014 Spasm of cervix uteri C2026907 Cervical spasm as antepartum condition UMLS C0002170 Alopecia disorders C0263491 Pili torti OrphaNet|MalaCards C0018991 Paralysis one side of body C3648261 Late effects of nontraumatic intracerebral hemorrhage hemiplegia UMLS C0013405 Dyspnea, paroxysmal C0039231 Tachycardia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0002453 Amenorrhea HSDN C0036572 Convulsion C0234972 Convulsive disorder UMLS C0518090 Frequency of pain question C0023487 Acute promyelocytic leukemia HSDN C0497406 Over weight C0022410 Joint instability HSDN C1304408 Urticarial vasculitis C0151436 Vasculitis, leukocytoclastic, cutaneous UMLS C4085317 Diarrhea frequency C0019569 Hirschsprung disease MalaCards|HSDN|HPO C4085211 Pain distress question C0030319 Panic disorder HSDN C0577567 Mass of urogenital structure C0007855 Cervical polyp UMLS C1963087 Constipation adverse event C0221043 Liddle syndrome OrphaNet|HPO|MalaCards C3898969 Have been vomiting C0020676 Hypothyroidism HSDN C2315100 Pediatric failure to thrive C0345893 Juvenile polyposis syndrome HPO C0042024 Urine incontinence C0022650 Kidney calculi HSDN C0040460 Dental pain C0997768 Glaucoma HSDN C0392678 Impaired swallowing C0006325 Bruxism UMLS C0012833 Dizzy C1145670 Respiratory failure HSDN C0151786 Weakness muscle C0036357 Psychology, schizophrenic HSDN C0015230 Exanthem C1858558 Rheumatoid arthritis, systemic juvenile MalaCards C1557397 Adverse event associated with pain C0701818 Choledocholithiasis HSDN C1963086 Confusion adverse event C0001973 Alcoholic intoxication, chronic HSDN C0085636 Light sensitivity C0003078 Aniseikonia HSDN C3887638 Failure to thrive in infant C3809522 Infantile liver failure syndrome 1 MalaCards C0518090 Frequency of pain question C0018023 Nodular goiter HSDN C0013404 Respiratory difficulty C0742746 Congestive heart failure decompensated UMLS C2984057 Have nausea C0042470 Guanarito haemorrhagic fever MalaCards C0000731 Abdomen distention C0010308 Congenital hypothyroidism OrphaNet|MalaCards C2315100 Pediatric failure to thrive C2931008 Congenital disorder of glycosylation type 2a MalaCards|HPO C0242936 Center pain C0035795 Fever mountain rocky spotted HSDN C1549543 Administration method - pain C0032320 Peritoneal free air HSDN C2984058 Have pain C0242188 Spider bites HSDN C0010200 Cough symptom C0023343 Leprosy HSDN C1963184 Nystagmus adverse event C1866039 Episodic ataxia, type 5 MalaCards C0162285 Edema eyelid C0002726 Amyloidosis OrphaNet|MalaCards C4084773 Bothered by weight gain C0037753 Sparganosis HSDN C0036572 Convulsion C0393691 Epilepsies, occipital lobe UMLS C0349588 Stature short C0086431 Hurler-scheie syndrome OrphaNet|HPO C0012569 Double vision C4085311 Depression - recess HSDN C4085211 Pain distress question C0037859 Spermatocele HSDN C0015468 Face pain C3494422 Retrognathias HSDN C0242936 Center pain C0023051 Laryngeal diseases HSDN C0018926 Emesis bloody C0011570 Mental depression HSDN C0013362 Dysarthrias C0004275 Attitude health HSDN C0020455 Hypergammaglobulinemia C0019618 Histiocytosis HSDN C0085636 Light sensitivity C0600467 Neurogenic inflammation HSDN C0008031 Pain chest C0008370 Cholestasis HSDN C0013404 Respiratory difficulty C1555914 Psychologist - psychotherapy, group HSDN C4084727 Cough frequency C0270611 Brain damage HSDN C1836296 Lower extremity weakness C0011860 Diabetes mellitus, non-insulin-dependent UMLS C2911647 Weight gain adverse event C0015923 Fetal alcohol syndrome HSDN C1963091 Diarrhea adverse event C0001815 Primary myelofibrosis HSDN C0036659 Sensation disorder C0003469 Anxiety disorders HSDN C0009806 Constipate C1963083 Cholecystitis adverse event HSDN C0030794 Pelvis pain C0004275 Attitude health HSDN C0018926 Emesis bloody C0023418 Leukemia HSDN C0030486 Extremity paralysis, lower C0751774 Nocturnal myoclonus syndrome HSDN C0042963 Symptoms vomiting C3272464 Ampulla of vater hepatoid adenocarcinoma UMLS C0011991 Loose stools C1847866 Homozygous 11p15-p14 deletion syndrome UMLS C2237041 Shox gene with short stature C0917990 Acro-osteolysis MalaCards C4084776 Weight loss C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0011991 Loose stools C0023493 Adult t-cell lymphoma/leukemia HSDN C0008031 Pain chest C0025229 Melioidosis DiseaseOntology|MalaCards C1971624 Appetite absent C0008049 Chicken pox DiseaseOntology|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0035793 Rocky mountain spotted fever HSDN C0239779 Grimacing C2677567 Dystonia 16 (disorder) MalaCards|UMLS C1557397 Adverse event associated with pain C0039730 Thalassemia HSDN C1963281 Vomiting adverse event C0003496 Aortic rupture HSDN C0002962 Angina C0027145 Myxedema HSDN C0917816 Deficiency mental C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C0030554 Abnormal sensation C0030305 Pancreatitis HSDN C0022660 Acute kidney failure C0153122 Induced malaria MalaCards C2187990 Unable to perform sex C1527231 Adrenomyeloneuropathy MalaCards|HPO C0018834 Brash C0279626 Squamous cell carcinoma of esophagus MalaCards C3887638 Failure to thrive in infant C0162530 Porphyria, erythropoietic HSDN C1557397 Adverse event associated with pain C1963120 Gynecomastia adverse event HSDN C0233794 Memory impaired C1863090 Alopecia, epilepsy, pyorrhea, mental subnormality OrphaNet|MalaCards C4084802 Usual severity diarrhea C0004239 Atrial flutter HSDN C0041834 Erythematous condition C3665732 Metastatic dermatofibrosarcoma protuberans MalaCards C0011991 Loose stools C0702166 Acne HSDN C1963091 Diarrhea adverse event C0036271 Scalp dermatoses HSDN C0018772 Deafness C0017612 Glaucoma, open-angle HSDN C1963077 Bone pain adverse event C0013366 Dyschondroplasia OrphaNet|HPO|MalaCards C4085549 Dizziness C0040100 Thymoma HSDN C4085548 Usual severity dizziness C0007282 Carotid stenosis HSDN C0860603 Anxiety symptom C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C1963252 Tremor adverse event C2674766 Myokymia 1 HPO C0349588 Stature short C3150926 Anemia, congenital dyserythropoietic, type iv HPO C0026826 High muscle tone C0206157 Myopathies, nemaline HSDN C4042891 Sleep wake disorders C0016724 Froehlich's syndrome HSDN C0015970 Fever unknown origin C0033578 Prostatic neoplasms HSDN C3463815 Feel fatigue C2984572 Malaria pathway HSDN C0023012 Delay language C4048800 Telomeric 22q13 monosomy syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C0014347 Enterobacteriaceae infections HSDN C1963180 Neck pain adverse event C0017601 Glaucomas HSDN C1557397 Adverse event associated with pain C0030521 Parathyroid neoplasms HSDN C0026838 Spasticity muscle C1706192 Sulfatidosis MalaCards C3463815 Feel fatigue C0559260 Congenital scoliosis HSDN C0013404 Respiratory difficulty C0036429 Sclerosis HSDN C0232466 Feeding difficulty C1970482 Potocki-lupski syndrome MalaCards C0001825 Agraphia C0344315 Depressed mood HSDN C0040034 Thrombocytopenia C0398650 Immune thrombocytopenic purpura OrphaNet|HPO|MalaCards C0002758 Anal or rectal pain C0740266 Anal and rectal conditions UMLS C0522224 Palsied C0027666 Neoplasms, radiation-induced HSDN C0427190 Ataxia, truncal C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0011991 Loose stools C0025269 Multiple endocrine neoplasia type 2b HPO|UMLS C1963086 Confusion adverse event C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1847839 Episodic ataxia, type 3 MalaCards C0018681 Headache, cephalalgia C0018671 Head and neck neoplasms HSDN C2919142 Short stature adverse event C2748516 Spondylodysplasia and premature pubarche HPO C0015672 Decreased energy C0037369 Smoking HSDN C0030193 Sense of pain C0037280 Skin diseases, parasitic HSDN C0232857 Psychogenic dysuria C0809986 Other mental conditions UMLS C0857305 Thrombocytopenia purpura C0020676 Hypothyroidism HSDN C2911647 Weight gain adverse event C0003507 Aortic valve stenosis HSDN C0010200 Cough symptom C0276108 Chlamydia infection psittaci HSDN C1384666 Decreased hearing C0026705 Mucopolysaccharidosis ii OrphaNet|HSDN C0018784 Deafness sensorineural C2931125 Feigenbaum bergeron richardson syndrome OrphaNet|MalaCards C0427068 Legs weakness C1853247 Spastic paraplegia 31, autosomal dominant MalaCards|HPO C0027497 Queasy C0520799 Acute radiation syndrome HSDN C1145670 Failure respiratory C1832661 Anophthalmia and pulmonary hypoplasia MalaCards|HPO C4085210 Usual severity pain C0043065 Water electrolyte imbalance HSDN C4084776 Weight loss C0002170 Alopecia HSDN C2919142 Short stature adverse event C1855849 Bartter syndrome, antenatal , type 2 HPO C3539022 Pelvic pain decreasing in severity C0009244 Behavioral cognitive therapy HSDN C0917816 Deficiency mental C0268543 Hyperammonemia, type iii MalaCards C0085631 Abnormal excitement C3714514 Infection HSDN C0040034 Thrombocytopenia C1863728 Hemophagocytic lymphohistiocytosis, familial, 4 MalaCards|HPO C2132198 Abnormal blistering of the skin C0235387 Porphyria type syndrome OrphaNet C0151786 Weakness muscle C3151519 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 MalaCards|HPO C0013395 Indigestion C0017168 Gastroesophageal reflux disease UMLS C0013604 Edematous C0032064 Plague HSDN C0018991 Paralysis one side of body C3648919 Hemiplegia affecting right nondominant side UMLS C0018991 Paralysis one side of body C0007798 Cerebral ventricle neoplasm HSDN C0042798 Vision dim C0001973 Alcoholic intoxication, chronic HSDN C1963184 Nystagmus adverse event C2930852 Zellweger leukodystrophy MalaCards C0242936 Center pain C0042266 Vaginismus HSDN C0242936 Center pain C0016171 Fistula of intestine, excluding rectum and anus HSDN C0349506 Sun sensitivity C0175691 Dubowitz syndrome MalaCards|HPO C1962972 Proteinuria adverse event C2931187 Nephropathic cystinosis MalaCards C0026838 Spasticity muscle C0268543 Hyperammonemia, type iii MalaCards C0015469 Facial paralysis C0016558 Forensic psychiatri HSDN C0037317 Sleep disturbance C0028064 Niemann-pick diseases MalaCards C0019209 Large liver C0037054 Sickle cell trait MalaCards C0026826 High muscle tone C1859468 Bird headed dwarfism montreal type OrphaNet|MalaCards C1145670 Failure respiratory C1867396 Radial-renal syndrome MalaCards C0022346 Yellow skin C1335315 Pancreatic serous cystadenocarcinoma UMLS C0020455 Hypergammaglobulinemia C0035328 Retinal vein occlusion HSDN C0018991 Paralysis one side of body C0878544 Cardiomyopathies HSDN C0332563 Papulae C1136041 Familial acoustic neuroma HPO C0030193 Sense of pain C3896673 Familial nonmedullary thyroid gland carcinoma MalaCards C0011991 Loose stools C0000833 Abscess HSDN C0015230 Exanthem C0346072 Blue rubber bleb nevus syndrome OrphaNet|HPO|MalaCards C4084788 Have dizziness C0520679 Sleep apnea, obstructive HSDN C0005745 Blepharoptosis C0175694 Smith-lemli-opitz syndrome OrphaNet|HPO|MalaCards C0018926 Emesis bloody C0003460 Anurias HSDN C2024878 Cardiovascular surgery result: dyspnea C0002875 Cooley's anemia OrphaNet|HPO C1527344 Dysphonia C2981150 Uranostaphyloschisis HSDN C0850149 Cough dry C0001175 Acquired immunodeficiency syndrome UMLS C0018681 Headache, cephalalgia C0272203 Indolent systemic mastocytosis OrphaNet|MalaCards C0034151 Hyperglobulinemic purpura C0026916 Mycobacterium avium-intracellulare infection HSDN C1963170 Hypothermia adverse event C1837371 Sudden infant death with dysgenesis of the testes syndrome OrphaNet|HPO|MalaCards C0332573 Macula C0399493 Amalgam tattooing UMLS C0037036 Increased salivation C0796222 Mental retardation, x linked 16 MalaCards|HPO C0013404 Respiratory difficulty C0008677 Bronchitis, chronic DiseaseOntology|MalaCards C0232466 Feeding difficulty C3151113 Meier-gorlin syndrome 3 MalaCards|HPO C0013404 Respiratory difficulty C0015397 Disorder of eye HSDN C4084725 Usual severity cough C0008924 Cleft lip HSDN C1557397 Adverse event associated with pain C0019284 Diaphragmatic hernia HSDN C0030232 Color loss C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0018772 Deafness C2931506 Stern lubinsky durrie syndrome MalaCards C3539892 Pelvic pain in front C0019294 Hernia, inguinal HSDN C1963087 Constipation adverse event C0024117 Chronic obstructive airway disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0006663 Calcinosis HSDN C1145670 Failure respiratory C0268338 Ehlers-danlos syndrome, type iv OrphaNet|HPO C0557874 Global developmental delay C0814154 Alcohol-related neurodevelopmental disorder OrphaNet|MalaCards C0151786 Weakness muscle C0268680 Biotin deficiency MalaCards C0036572 Convulsion C0041296 Tuberculosis UMLS C0033377 Caudal displacement C0265226 Hecht syndrome (disorder) HPO C0575081 Abnormal gait C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|HPO|MalaCards C0012833 Dizzy C0002940 Aneurysm HSDN C1565249 Limitation, mobility C0022821 Kyphosis deformity of spine HSDN C0349588 Stature short C1856871 Aarskog-like syndrome OrphaNet|MalaCards C2237041 Shox gene with short stature C1839311 Scott bryant graham syndrome OrphaNet|MalaCards C0024902 Mastodynia C1963064 Anxiety adverse event HSDN C0008031 Pain chest C0038661 Suicide HSDN C0019825 Voice hoarseness C0206765 Connective and soft tissue neoplasm HSDN C1961131 Cough adverse event C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C0013362 Dysarthrias C2750442 Hypermanganesemia with dystonia polycythemia and cirrhosis HPO C1963071 Back pain adverse event C0021890 Intraoperative complications HSDN C2315100 Pediatric failure to thrive C0015923 Fetal alcohol syndrome HSDN C0011991 Loose stools C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C3887638 Failure to thrive in infant C3150344 Hyperhomocysteinemia, thrombotic, cbs-related HPO C4084769 Vomiting frequency C0043241 Wound infection HSDN C0018991 Paralysis one side of body C0009244 Behavioral cognitive therapy HSDN C0151786 Weakness muscle C0751194 Hematoma, spinal subdural HSDN C4085317 Diarrhea frequency C0016978 Gallbladder neoplasm HSDN C0002170 Alopecia disorders C0268425 Alstrom syndrome MalaCards|HPO C2198882 Disturbing or unusual thoughts, feelings, or sensations C0011551 Depersonalisation UMLS C1384666 Decreased hearing C1970479 Branchiootorenal syndrome 2 MalaCards|HPO C1557397 Adverse event associated with pain C0037413 Social dominance HSDN C0040460 Dental pain C0024081 Angina, ludwig HSDN C0522044 Thigh edema C0740728 Lower extremity problem UMLS C0020649 Blood pressure decreased C0852654 21-hydroxylase deficiency MalaCards C3829611 Nausea frequency C0038379 Eye deviation HSDN C0221263 Cafe au lait spot C0025299 Meningocele HSDN C0017181 Gastrointestinal bleed C3179396 Glanzmann thrombasthenia, type a MalaCards C4084725 Usual severity cough C0001122 Acidosis HSDN C0019079 Bloody sputum C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C1963091 Diarrhea adverse event C0004610 Bacteremia HSDN C2984058 Have pain C0030977 Perceptual masking HSDN C4084724 Usual severity constipation C1997362 Non-neurogenic neurogenic bladder MalaCards C0011991 Loose stools C0019693 Hiv infections DiseaseOntology|HSDN|MalaCards C0018681 Headache, cephalalgia C3897748 Recurrent childhood oligoastrocytoma UMLS C1963180 Neck pain adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0015672 Decreased energy C0015461 Facial neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1504665 Products used to treat diabetic ketoacidosis HSDN C0018681 Headache, cephalalgia C0338485 Non-familial hemiplegic migraine UMLS C0557874 Global developmental delay C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C1384666 Decreased hearing C2829267 Deafness, autosomal recessive 88 MalaCards C1961131 Cough adverse event C0011265 Presenile dementia HSDN C0009676 Confusion state C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C0018772 Deafness C3888317 Sialidosis, type 2 OrphaNet C0005779 Clotting C1848214 Heterotopia, periventricular nodular, with frontometaphyseal dysplasia HPO C0751840 Pure alexia C0398625 Protein c deficiency HSDN C0151786 Weakness muscle C0006309 Brucellosis HSDN C0002962 Angina C0033968 Psychotherapeutic technique HSDN C0000737 Abdomen pain C0243001 Abdominal abscess UMLS C1384666 Decreased hearing C0023944 Cerebromedullospinal disconnection MalaCards C1963091 Diarrhea adverse event C0017185 Gastrointestinal neoplasms HSDN C0848203 Male pelvic pain C0600041 Infective cystitis HSDN C0002963 Angina variant C0004096 Asthma HSDN C0007758 Cerebellar ataxia C0268251 Gaucher disease, type 3 (disorder) OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C1864041 Cerebral cavernous malformations 2 HPO C1963180 Neck pain adverse event C0027809 Neurilemmoma HSDN C0040264 Ear ringing sound C1290398 Cerebral arterial aneurysm HSDN C2024878 Cardiovascular surgery result: dyspnea C0040053 Thrombosis HSDN C0151889 Reflexes tendon increased C3554209 Pontocerebellar hypoplasia, type 8 MalaCards C2911647 Weight gain adverse event C0030567 Parkinson disease HSDN C0008031 Pain chest C0002886 Anemia, macrocytic UMLS C0042963 Symptoms vomiting C0015814 Femur head necrosis HSDN C3829611 Nausea frequency C0520946 Emotional hypersensitivity HSDN C0018772 Deafness C0796117 Pitt syndrome MalaCards C2242996 Tingling C0020550 Hyperthyroidism HSDN C0028738 Nystagmus C0029534 Other cerebellar ataxia MalaCards C1961131 Cough adverse event C0243026 Sepsis HSDN C0522224 Palsied C0751792 Trauma, nervous system HSDN C0413252 Hypothermia due to exposure C0039006 Swine--diseases HSDN C0033377 Caudal displacement C1864436 Muenke syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0031154 Peritonitis HSDN C0002622 Amnesias C0022336 Creutzfeldt-jakob disease MalaCards C4084784 Diarrhea C0021345 Infectious mononucleosis HSDN C0015469 Facial paralysis C1858118 Muscular dystrophy, congenital, 1b MalaCards C1963091 Diarrhea adverse event C0597109 Nurse's role HSDN C4084767 Bothered by vomiting C0043019 Lateral medullary syndrome HSDN C0041657 Consciousness loss C0004364 Autoimmune diseases HSDN C0151786 Weakness muscle C0020598 Hypocalcemia HSDN C1384666 Decreased hearing C1836544 Schindler disease, type i OrphaNet|HPO|MalaCards C0013390 Cramps menstrual C0037274 Dermatologic disorders HSDN C0522224 Palsied C0002880 Autoimmune hemolytic anemia HSDN C1963175 Sinus bradycardia adverse event C1833154 Long qt syndrome 4 MalaCards|HPO C0022346 Yellow skin C1335458 Postsurgical stage iii hepatoblastoma UMLS C0030552 Paralysis partial C0085404 Poems syndrome MalaCards|HSDN C0518090 Frequency of pain question C0020557 Hypertriglyceridemia HSDN C4084769 Vomiting frequency C0006267 Bronchiectasis HSDN C0009421 Comatose C0037744 Perceptual spatial orientation HSDN C0013404 Respiratory difficulty C0017178 Gastrointestinal diseases HSDN C0015672 Decreased energy C1552527 Clinic / center - developmental disabilities HSDN C1963063 Anorexia adverse event C0206698 Cholangiocarcinoma HPO C1549543 Administration method - pain C0043241 Wound infection HSDN C0002962 Angina C0024205 Lymphadenitis HSDN C4084773 Bothered by weight gain C0023176 Lead poisoning HSDN C0424755 Fever symptoms C0039981 Thoracic neoplasms HSDN C4085317 Diarrhea frequency C2931788 Atypical hemolytic uremic syndrome MalaCards C0037763 Spasm C0037768 Spasmophilia UMLS C3665386 Abnormal vision C1527406 Rhizomelic pseudopolyarthritis MalaCards C4084802 Usual severity diarrhea C0040843 Treponemal disease HSDN C1963063 Anorexia adverse event C0040948 Trichostrongyliasis HSDN C0030193 Sense of pain C0027708 Nephroblastoma HSDN C1961131 Cough adverse event C0403447 Chronic kidney insufficiency HSDN C4084897 Sleep disturbance subordinate domain C0086649 Mps iii c HPO C1963093 Dizziness adverse event C0206255 Malaria vaccine HSDN C1963281 Vomiting adverse event C0220710 Medium-chain acyl-coenzyme a dehydrogenase deficiency HPO C3463815 Feel fatigue C0014836 Escherichia coli infections HSDN C1384666 Decreased hearing C0029878 Otitis externa HSDN C1962972 Proteinuria adverse event C0001969 Alcoholic intoxication HSDN C1279888 Proteinuria of undiagnosed cause C0740340 Amyloidosis, familial HSDN C0557874 Global developmental delay C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0206754 Neuroendocrine tumors HSDN C0004134 Dyssynergia C0239981 Hypoalbuminemia HSDN C2237041 Shox gene with short stature C2675875 Chromosome 2p16.1 p15 deletion syndrome MalaCards C4042891 Sleep wake disorders C0011609 Drug eruptions HSDN C0344315 Mood depressed C1527406 Rhizomelic pseudopolyarthritis MalaCards C0000737 Abdomen pain C2711591 Infection by anisakidae MalaCards C3463815 Feel fatigue C0029456 Osteoporosis HSDN C0037316 Not enough sleeping C3827868 Tachycardia by ecg finding HSDN C4085317 Diarrhea frequency C0024788 Green monkey virus disease DiseaseOntology|OrphaNet|MalaCards C0042963 Symptoms vomiting C0031090 Periodontal diseases HSDN C0013604 Edematous C0024299 Lymphoma HSDN C1557397 Adverse event associated with pain C1963090 Dehydration adverse event HSDN C0018520 Breath odor C0036341 Schizophrenia HSDN C3274924 Have been coughing C0887976 Chlamydophila infections HSDN C3203358 Alveolar hypoventilation C0023903 Liver neoplasms HSDN C0015300 Ocular proptosis C2931196 Craniofacial dysostosis type 1 MalaCards C0018784 Deafness sensorineural C0004610 Bacteremia HSDN C0003550 Broca aphasia C2984299 Asthma pathway HSDN C1145670 Failure respiratory C2931226 Thompson baraitser syndrome OrphaNet|MalaCards C3146279 Coma C0007222 Cardiovascular diseases HSDN C1963065 Apnea adverse event C1835614 Hereditary hyperexplexia HPO C0013604 Edematous C0007786 Brain ischemia HSDN C0424755 Fever symptoms C0015404 Eye infections, bacterial HSDN C2911645 Weight loss adverse event C0041313 Hepatic tuberculosis DiseaseOntology|MalaCards C2108109 Continuous electrocardiogram sinus tachycardia C0033300 Progeria HPO C0030193 Sense of pain C0343214 Painful arc syndrome UMLS C0036572 Convulsion C3275487 Cerebral-cerebellar-coloboma syndrome, x-linked MalaCards|UMLS C0009806 Constipate C0268381 Primary amyloidosis OrphaNet C1963170 Hypothermia adverse event C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0026838 Spasticity muscle C0042035 Urination disorders HSDN C0242936 Center pain C3150878 Hyperoxaluria, primary, type iii MalaCards C2984057 Have nausea C0243026 Sepsis HSDN C1963091 Diarrhea adverse event C0041234 Chagas disease OrphaNet|MalaCards C3641755 Have constipation C1836522 Schindler disease, type ii MalaCards C3203358 Alveolar hypoventilation C3203358 Hypoventilation MalaCards C2024893 Cardiovascular surgery result: fatigue C0036221 Mast-cell sarcoma OrphaNet|MalaCards C0011570 Monopolar depression C1856492 Gaucher disease, type iiib HPO C1962972 Proteinuria adverse event C0021568 Bites insect stings HSDN C4084769 Vomiting frequency C0032131 Plasmacytoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041234 Chagas disease HSDN C0242670 Chronic vegetative state C0032787 Postoperative complications HSDN C0424755 Fever symptoms C0406645 Amyopathic dermatomyositis MalaCards C1962956 Flatulence adverse event C0162429 Malnutrition HSDN C0004134 Dyssynergia C0393593 Dystonia disorders HSDN C0028084 Terrifying dreams C3887605 Dream anxiety disorders UMLS C0020672 Body temperature decreased C1963083 Cholecystitis adverse event HSDN C0086565 Liver function abnormal C0917713 Becker muscular dystrophy OrphaNet|HPO C1962972 Proteinuria adverse event C0037928 Spinal cord diseases HSDN C1963281 Vomiting adverse event C0428977 Bradycardia HSDN C2362324 Pediatric obesity C0013473 Eating disorders HSDN C1963091 Diarrhea adverse event C0038587 Substance withdrawal syndrome HSDN C2242996 Tingling C0007682 Cns disorder HSDN C1963247 Ventricular tachycardia adverse event C1858379 Arrhythmogenic right ventricular dysplasia, familial, 5 (disorder) HPO C4085317 Diarrhea frequency C0018889 Helminthiasis HSDN C2984057 Have nausea C1548578 Location characteristic id - smoking HSDN C0019209 Large liver C3552634 Lymphoproliferative syndrome 1 MalaCards C0026838 Spasticity muscle C0037047 Sibling HSDN C0151786 Weakness muscle C0220654 Meningeal carcinomatosis HSDN C0013604 Edematous C0002170 Alopecia HSDN C0016927 Gag reflex C0007820 Cerebrovascular disorders HSDN C0024032 Birth weight subnormal C2931557 Chromosome 4 short arm deletion MalaCards C0015672 Decreased energy C1336075 Splenic small lymphocytic lymphoma UMLS C0030193 Sense of pain C0041428 Twin siamese HSDN C0518090 Frequency of pain question C0039747 Thecoma HSDN C0015672 Decreased energy C0343068 Familial cold urticaria OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C1263846 Attention deficit hyperactivity disorder HSDN C0476273 Distress respiratory C0024117 Chronic obstructive airway disease UMLS C0018784 Deafness sensorineural C1853623 Fryns-aftimos syndrome MalaCards C1557397 Adverse event associated with pain C0311389 Nonspecific urethritis HSDN C1527344 Dysphonia C0032787 Postoperative complications HSDN C0037036 Increased salivation C1848211 Mental retardation with psychosis, pyramidal signs, and macroorchidism MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C1970470 Surfactant metabolism dysfunction, pulmonary, 2 (disorder) MalaCards C0016204 Fart C0812393 Cancer patients and suicide and depression HSDN C0035229 Respiratory function impaired C0024899 Mastocytosis MalaCards C3641756 Have diarrhea C0268328 Porphobilinogen synthase deficiency MalaCards C0040822 D tremors C0004135 Ataxia telangiectasia OrphaNet|UMLS|HPO|MalaCards C4084784 Diarrhea C0014170 Endometrial neoplasms HSDN C0557874 Global developmental delay C2930917 Chromosome 14, trisomy mosaic OrphaNet|MalaCards C0011168 Disorder deglutition C1443901 Intestinal botulism OrphaNet|MalaCards C3665346 Loss sight C2931386 Amaurosis congenita of leber, 3 MalaCards C0020672 Body temperature decreased C0014556 Epilepsy, temporal lobe HSDN C0018681 Headache, cephalalgia C0948264 Neuroborreliosis MalaCards C0023222 Lower extremity pain musculoskeletal C0037773 Spastic paraplegia, hereditary UMLS C0042024 Urine incontinence C0006840 Candidiasis HSDN C0024031 Back pain lower back C0017185 Gastrointestinal neoplasms HSDN C0497406 Over weight C0033578 Prostatic neoplasms HSDN C0018926 Emesis bloody C0221018 Hereditary sideroblastic anemia HSDN C0018681 Headache, cephalalgia C0000809 Abortion, habitual HSDN C0917816 Deficiency mental C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C2919142 Short stature adverse event C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C0032339 Rothmund-thomson syndrome OrphaNet|HPO|MalaCards C1971624 Appetite absent C0017601 Glaucomas HSDN C3887638 Failure to thrive in infant C2931850 Aase smith syndrome 2 MalaCards|HPO C0009421 Comatose C0472377 Basal ganglia hemorrhage HSDN C4084776 Weight loss C0033046 Premenstrual syndrome HSDN C0028738 Nystagmus C3165526 Congenital iodine deficiency syndrome MalaCards C4084766 Vomiting C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0011168 Deglutition disorders HSDN C4084802 Usual severity diarrhea C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038017 Congenital spondylolisthesis HSDN C0012833 Dizzy C0024299 Lymphoma HSDN C2984058 Have pain C0019421 Heterosexual behavior HSDN C2911647 Weight gain adverse event C0085271 Self-injurious behavior HSDN C0036572 Convulsion C0271742 Glucocorticoid deficiency with achalasia OrphaNet|HPO C4050613 Anxiety C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0242936 Center pain C0546952 Congenital facial asymmetry HSDN C0231341 Aging premature C0029411 Osteoarthropathy, primary hypertrophic HSDN C3887873 Hearing loss C3813607 Infantile gastroesophageal reflux HSDN C0002962 Angina C0085096 Peripheral vascular diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C0019196 Hepatitis c HSDN C0036659 Sensation disorder C0399526 Class iii malocclusion HSDN C4085862 Bothered by nausea C0019069 Hemophilia a HSDN C0017181 Gastrointestinal bleed C0001733 Afibrinogenemia MalaCards C4084773 Bothered by weight gain C2219717 Menstrual periods stopped for over 6 months HSDN C0027796 Neuralgias C0019310 Hernia, obturator HSDN C4084774 Have weight loss C0270611 Brain damage HSDN C0009676 Confusion state C0749095 Subdural hematoma chronic HSDN C0034124 Pupillary disorder C0019360 Herpes zoster disease HSDN C4085222 Nausea C3495422 Finding relating to sexuality and sexual activity HSDN C4085211 Pain distress question C0700345 Candidiasis, vulvovaginal HSDN C0030193 Sense of pain C0035328 Retinal vein occlusion HSDN C0242936 Center pain C1962974 Chylothorax adverse event HSDN C0344315 Mood depressed C0002875 Cooley's anemia OrphaNet|HPO C0038990 Sweats C3809006 Cardiofaciocutaneous syndrome 3 MalaCards C0518090 Frequency of pain question C0275148 Poisoning of animal by plant HSDN C0206160 Retic count elevated C1836705 Pseudohyperkalemia, familial, 2, due to red cell leak MalaCards|HPO C4085317 Diarrhea frequency C0267941 Pancreatitis, acute necrotizing HSDN C0024032 Birth weight subnormal C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C0009421 Comatose C0016542 Foreign body HSDN C0030554 Abnormal sensation C0022665 Kidney neoplasm HSDN C1961131 Cough adverse event C0023241 Legionnaires' disease OrphaNet|MalaCards C1963086 Confusion adverse event C0029408 Degenerative polyarthritis HSDN C0349588 Stature short C0152096 Complete trisomy 18 syndrome OrphaNet|MalaCards C4084768 Usual severity vomiting C0334092 Hamartomatous polyp MalaCards C0031911 Pigment deposition C0023269 Leiomyosarcoma MalaCards C3539889 Pelvic pain increasing in severity C0041311 Tuberculosis, female genital HSDN C1549543 Administration method - pain C0003723 Arbovirus infections HSDN C1961131 Cough adverse event C0162526 Aids-related opportunistic infections HSDN C0080233 Dental loss C0032339 Rothmund-thomson syndrome MalaCards C0413252 Hypothermia due to exposure C0031212 Personality disorders HSDN C0349588 Stature short C0029455 Osteopoikilosis (disorder) OrphaNet|HPO|MalaCards C4084784 Diarrhea C0039446 Telangiectasis HSDN C4085211 Pain distress question C0020097 Htlv-i infections HSDN C4084773 Bothered by weight gain C0241158 Cicatrix skin HSDN C0242936 Center pain C3714644 Thymus neoplasms HSDN C0344428 Ventricular tachycardia by ecg finding C3150690 Left ventricular noncompaction 5 MalaCards C0034150 Skin purpura C2973529 Leukocytoclastic vasculitis MalaCards C1963137 Hydrocephalus adverse event C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards C1565249 Limitation, mobility C0344434 Atrial fibrillation ecg HSDN C0009676 Confusion state C0268543 Hyperammonemia, type iii MalaCards|HPO C0034150 Skin purpura C0018798 Congenital heart defects HSDN C4085317 Diarrhea frequency C0036216 Sarcoma, experimental HSDN C0013404 Respiratory difficulty C0010823 Cytomegalovirus infections HSDN C2911645 Weight loss adverse event C1262481 Eosinophilic gastroenteritis MalaCards C1962972 Proteinuria adverse event C0877024 Schimke immunoosseous dysplasia OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0042961 Intestinal volvulus HSDN C0013604 Edematous C0752130 Spinal cord ischemia HSDN C0019825 Voice hoarseness C0268543 Hyperammonemia, type iii MalaCards C0030193 Sense of pain C0024904 Mastoiditis HSDN C0004604 Pain back C0034931 Reflex sympathetic dystrophy HSDN C2700617 Irritation - emotion C0010481 Cushing syndrome OrphaNet|MalaCards C2984058 Have pain C1956089 Osteophyte HSDN C1565249 Limitation, mobility C0751813 Chronic brain injury HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006110 Brain death HSDN C0000737 Abdomen pain C1518873 Pancreatic intraductal papillary mucinous neoplasm with high grade dysplasia UMLS C1850830 Exercise-induced muscle pain C1832560 Rippling muscle disease 2 MalaCards|HPO C4085210 Usual severity pain C0002448 Ameloblastoma HSDN C0024031 Back pain lower back C0026769 Multiple sclerosis HSDN C0026838 Spasticity muscle C0021390 Inflammatory bowel diseases HSDN C2984057 Have nausea C0039730 Thalassemia HSDN C1963091 Diarrhea adverse event C1865372 Athabaskan severe combined immunodeficiency HPO C0015672 Decreased energy C1833372 Hypocalciuric hypercalcemia, familial, type iii MalaCards C2984058 Have pain C0030567 Parkinson disease HSDN C0003469 Anxiety disorder C1384514 Conn syndrome MalaCards C0344315 Mood depressed C1843852 Spinocerebellar ataxia with epilepsy HPO C0019079 Bloody sputum C4050613 Anxiety scale (basc-2) HSDN C4084784 Diarrhea C0015397 Disorder of eye HSDN C3539022 Pelvic pain decreasing in severity C2936290 Femoracetabular impingement HSDN C0242936 Center pain C0041311 Tuberculosis, female genital HSDN C2911645 Weight loss adverse event C0018916 Hemangioma HSDN C0018524 Hallucinate C0031511 Pheochromocytoma HSDN C3539891 Pelvic pain to the rear C0007860 Uterine cervicitis HSDN C1961131 Cough adverse event C0024232 Lymphatic metastasis HSDN C3274924 Have been coughing C0018273 Growth disorders HSDN C0231341 Aging premature C0403447 Chronic kidney insufficiency HSDN C0022107 Fussiness C2931919 X-linked infantile spasm syndrome MalaCards C1963067 Atrial fibrillation adverse event C0410226 Congenital myotonic dystrophy MalaCards C0009806 Constipate C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0557874 Global developmental delay C1853102 Cerebrooculofacioskeletal syndrome 2 MalaCards|HPO C1963137 Hydrocephalus adverse event C0796033 Marden-walker syndrome MalaCards C4084769 Vomiting frequency C0162820 Dermatitis, allergic contact HSDN C0023012 Delay language C1837475 Insulin-like growth factor i deficiency MalaCards C4085210 Usual severity pain C0011311 Dengue fever HSDN C0700078 Deep tendon reflex decrease C3281202 Mental retardation, autosomal dominant 13 MalaCards C0557874 Global developmental delay C2931197 Waaler aarskog syndrome MalaCards C0015676 Mental fatigue C0079173 Craniomandibular disorders HSDN C3898969 Have been vomiting C3714509 Nutrition disorders HSDN C0007758 Cerebellar ataxia C0344467 Biemond syndrome MalaCards C4085211 Pain distress question C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C4085211 Pain distress question C0018671 Head and neck neoplasms HSDN C4085661 Usual severity nausea C1963215 Pneumothorax adverse event HSDN C0151686 Growth retardation C0342765 D-glyceric aciduria HPO C0151827 Pain eye C0017653 Glomus tumor HSDN C0030486 Extremity paralysis, lower C1963137 Hydrocephalus adverse event HSDN C0011206 Delirium acute C0042373 Vascular diseases HSDN C0242936 Center pain C0002902 Anencephaly HSDN C0023014 Developmental disorder language C0014544 Epilepsy HSDN C3814530 Skin vesicle C0011608 Dermatitis herpetiformis OrphaNet|MalaCards C0007758 Cerebellar ataxia C0796202 Wittwer syndrome MalaCards C3541349 Syncope C0000768 Congenital abnormality HSDN C0917801 Sleep disorder insomnia C0751254 Creutzfeldt-jakob disease, familial MalaCards C0013604 Edematous C0022650 Kidney calculi HSDN C0018681 Headache, cephalalgia C0040336 Tobacco use disorder HSDN C1963071 Back pain adverse event C0033348 Language program HSDN C0015672 Decreased energy C0314657 Genetic predisposition HSDN C2024893 Cardiovascular surgery result: fatigue C0013720 Ehlers-danlos syndrome HSDN C0221752 Rbc urine C0019034 Hemoglobin sc disease MalaCards C0020615 Hypoglycemia nos C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C3641756 Have diarrhea C0023798 Lipoma HSDN C0917816 Deficiency mental C3150939 Beaulieu-boycott-innes syndrome MalaCards|HPO C0004134 Dyssynergia C1851708 Encephalopathy, recurrent, of childhood MalaCards C0018681 Headache, cephalalgia C3897752 Recurrent childhood glioblastoma UMLS C0040485 Wryneck C0022738 Klippel-feil syndrome HSDN C4085211 Pain distress question C0221056 Adult type dermatomyositis HSDN C4084784 Diarrhea C0009021 Clonorchiasis DiseaseOntology C2984058 Have pain C0018199 Granuloma, plasma cell HSDN C0233514 Behavior abnormal C0271889 Diencephalic syndrome of infancy OrphaNet|MalaCards C1963252 Tremor adverse event C0027051 Myocardial infarction HSDN C0033774 Skin pruritus C0497580 Condylomata acuminata in men HSDN C3163620 Hypotension adverse event C0024899 Mastocytosis MalaCards C2984058 Have pain C0020621 Hypokalemia HSDN C0020450 Hyperemesis gravidarum C0008493 Hydatidiform mole, invasive HSDN C1069915 Vertigo C0085541 Epilepsy, frontal lobe HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0221757 Alpha 1-antitrypsin deficiency HSDN C4084766 Vomiting C0019372 Herpesviridae infections HSDN C0000737 Abdomen pain C2963140 Arteriovenous fistula in use with two needles HSDN C3641756 Have diarrhea C0025289 Meningitis HSDN C0041105 Jaw spasm C0011581 Depressive disorder HSDN C3641756 Have diarrhea C1254288 Anthrax HSDN C1384666 Decreased hearing C0009475 Community mental health service HSDN C0020673 Hypothermia (central) (local) C1269683 Major depressive disorder HSDN C3541349 Syncope C0796561 Melanoma vaccines HSDN C0027066 Myoclonic jerking C0034530 Injury radiation HSDN C4085211 Pain distress question C0005937 Bone cysts HSDN C0036572 Convulsion C2931050 Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies OrphaNet C4255193 Bilateral vestibulopathy C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards C1860844 Sparse, thin hair C1859385 Anodontia-hypotrichosis syndrome MalaCards C4084725 Usual severity cough C0023267 Fibroid tumor HSDN C0085636 Light sensitivity C1962986 Glaucoma adverse event HSDN C0016199 Pain flank C0043253 Trauma blunt HSDN C0030193 Sense of pain C1561518 Pleasure - animals raised for recreation HSDN C1963249 Tinnitus adverse event C0003467 Anxiety HSDN C4084784 Diarrhea C0005745 Blepharoptosis HSDN C1963087 Constipation adverse event C0037274 Dermatologic disorders HSDN C0034933 Abnormal reflexes C0019080 Hemorrhage HSDN C0018772 Deafness C3888337 Deafness, autosomal recessive 96 MalaCards C0011991 Loose stools C0025958 Microcephaly HSDN C1279888 Proteinuria of undiagnosed cause C0029443 Osteomyelitis HSDN C0242936 Center pain C0017924 Glycogen storage disease type v HSDN C0003113 Anomia C0024761 Communication, manual HSDN C0518090 Frequency of pain question C0018671 Head and neck neoplasms HSDN C2919142 Short stature adverse event C2931302 Familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails OrphaNet|MalaCards C0917816 Deficiency mental C2751938 Cerebral palsy, spastic quadriplegic, 1 MalaCards|HPO C1963087 Constipation adverse event C0919267 Ovarian neoplasm HSDN C4084773 Bothered by weight gain C0035358 Retroperitoneal neoplasm HSDN C3463815 Feel fatigue C0700095 Central neuroblastoma HSDN C4085211 Pain distress question C0018944 Hematoma HSDN C0018772 Deafness C0019159 Hepatitis a HSDN C0026826 High muscle tone C0878588 Sphincter oddi dysfunction HSDN C0013378 Dysgensia C0011168 Deglutition disorders HSDN C4084766 Vomiting C0000809 Abortion, habitual HSDN C0013395 Indigestion C0853698 Lymphocytes increased HSDN C0010038 Corneal opacity disorder C0268250 Gaucher disease, type 2 (disorder) MalaCards C0746674 Muscle weakness generalized C1834336 Nemaline myopathy 3 HPO|UMLS C0007398 Catatonic C0007771 Intracranial arteriosclerosis HSDN C1963281 Vomiting adverse event C0015401 Foreign body in eye HSDN C0024031 Back pain lower back C0026764 Multiple myeloma HSDN C0018772 Deafness C0027341 Nail-patella syndrome MalaCards|HPO C4084773 Bothered by weight gain C0021364 Male infertility HSDN C4085549 Dizziness C0007570 Celiac disease HSDN C0040264 Ear ringing sound C1999266 Depression adverse event HSDN C2203646 Jaundice C0270210 Lucey-driscoll syndrome (disorder) HPO C0010200 Cough symptom C0149721 Left ventricular hypertrophy HSDN C0019825 Voice hoarseness C0026269 Mitral valve stenosis HSDN C0013394 Coitus painful C0206680 Mesothelioma, cystic OrphaNet|MalaCards C1549543 Administration method - pain C0079218 Fibromatosis, aggressive HSDN C0000737 Abdomen pain C0029307 Oroya fever MalaCards C0344315 Mood depressed C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0015672 Decreased energy C0023903 Liver neoplasms MalaCards C4042891 Sleep wake disorders C0027073 Myofascial pain syndromes HSDN C4084774 Have weight loss C0011265 Presenile dementia HSDN C0035078 Failure kidney C0079583 Ichthyosiform erythroderma, congenital MalaCards C3539023 Pelvic pain increasing in frequency C0009244 Behavioral cognitive therapy HSDN C0000737 Abdomen pain C0080304 Vascular fistula HSDN C0426396 Dark urine C0085293 Hepatitis e MalaCards C2984057 Have nausea C0679360 Foodborne disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0038160 Staphylococcal infections HSDN C0039870 Leanness C0235461 Androgen excess HSDN C0000737 Abdomen pain C3273136 Intrahepatic bile duct papillary neoplasm with an associated invasive carcinoma UMLS C4084766 Vomiting C0021368 Inflammation HSDN C0008031 Pain chest C1334636 Mature mediastinal teratoma UMLS C0035078 Failure kidney C1867774 Sacral agenesis syndrome HPO C0036572 Convulsion C3150756 Chromosome 4q21 deletion syndrome MalaCards C3541349 Syncope C0014863 Esophageal spasm diffuse HSDN C0151786 Weakness muscle C0001721 Emotional affect HSDN C1279888 Proteinuria of undiagnosed cause C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C1963252 Tremor adverse event C0009324 Ulcerative colitis HSDN C0036572 Convulsion C2675336 Duplication 15q11-q13 syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0008521 Choroid diseases HSDN C4084723 Constipation C0034069 Pulmonary fibrosis HSDN C4084724 Usual severity constipation C0393571 Multiple system atrophy HSDN C3887873 Hearing loss C0002940 Aneurysm HSDN C4084774 Have weight loss C0023860 Listeriosis HSDN C0413252 Hypothermia due to exposure C0037274 Dermatologic disorders HSDN C0040264 Ear ringing sound C0020676 Hypothyroidism HSDN C1549543 Administration method - pain C0013418 Abnormal labor HSDN C3539889 Pelvic pain increasing in severity C0017181 Gastrointestinal hemorrhage HSDN C0037316 Not enough sleeping C0520946 Emotional hypersensitivity HSDN C2315100 Pediatric failure to thrive C2673609 Epidermolysis bullosa inversa dystrophica MalaCards C0004604 Pain back C0013922 Embolism HSDN C0020458 Hyperhydrosis C0346303 Thyrotroph adenoma OrphaNet|MalaCards C0011991 Loose stools C1367460 Lats1 gene HSDN C2984058 Have pain C0008073 Developmental disabilities HSDN C3887638 Failure to thrive in infant C3889576 Euphoria HSDN C0002965 Crescendo angina C0040034 Thrombocytopenia HSDN C4042891 Sleep wake disorders C1963266 Uveitis adverse event HSDN C0242670 Chronic vegetative state C0162869 Aneurysm, ruptured HSDN C1557397 Adverse event associated with pain C1254288 Anthrax HSDN C0018965 Blood urine C0342750 Glycogen storage disease type id MalaCards|HPO C0018784 Deafness sensorineural C1762616 Meningioma, benign, no icd-o subtype HSDN C0030193 Sense of pain C4075706 Post-infectious segmental neuralgia UMLS C4085210 Usual severity pain C3714644 Thymus neoplasms HSDN C0150055 Pain chronic C0001529 Dercum disease MalaCards|UMLS C0314719 Dry eyes C0013238 Dry eye syndromes UMLS C0018965 Blood urine C0878681 Dent's disease OrphaNet C0851578 Disorder sleep C0037397 Behavior social HSDN C1000483 Genus anemia C2675512 Diamond-blackfan anemia 7 MalaCards C0010200 Cough symptom C0025060 Mediastinal cyst HSDN C0028738 Nystagmus C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism OrphaNet|MalaCards C0018681 Headache, cephalalgia C0700367 Ependymoblastoma UMLS C0009676 Confusion state C0014547 Epilepsies, partial HSDN C0011991 Loose stools C0021799 Interprofessional relations HSDN C0013362 Dysarthrias C1969645 Ataxia, spastic, 3, autosomal recessive MalaCards|HPO C1549543 Administration method - pain C0020649 Hypotension HSDN C0018681 Headache, cephalalgia C1367536 Nasopharyngeal angiofibroma UMLS C0557874 Global developmental delay C2751938 Cerebral palsy, spastic quadriplegic, 1 MalaCards|HPO C0002962 Angina C0004626 Pneumonia, bacterial HSDN C0086132 Depression symptom C0011570 Mental depression UMLS C1963086 Confusion adverse event C0041755 Adverse reaction to drug HSDN C0024031 Back pain lower back C0001621 Adrenal gland diseases HSDN C2984058 Have pain C0023176 Lead poisoning HSDN C0557874 Global developmental delay C0034341 Pyruvate carboxylase deficiency disease MalaCards|HPO C0030554 Abnormal sensation C1274879 Port-wine stain with oculocutaneous melanosis OrphaNet|MalaCards C2911647 Weight gain adverse event C0582587 Visual learning HSDN C0030193 Sense of pain C0032580 Adenomatous polyposis coli HSDN C0270948 Neurogenic muscular atrophy C1857339 Deafness, congenital, with vitiligo and achalasia MalaCards C0232466 Feeding difficulty C0342705 Folate malabsorption, hereditary MalaCards C3463815 Feel fatigue C0085278 Antiphospholipid syndrome HSDN C0016382 Cutaneous vascular engorgement C0014548 Epilepsy, generalized HSDN C0026858 Musculoskeletal pain C0037286 Skin neoplasms HSDN C3463815 Feel fatigue C0085096 Peripheral vascular diseases HSDN C0011991 Loose stools C1565489 Renal insufficiency HSDN|UMLS C0026205 Pupillary constriction C0017601 Glaucomas HSDN C0027498 Nausea vomiting C0035436 Rheumatic fever OrphaNet|MalaCards C0033377 Caudal displacement C1838162 Mesomelia-synostoses syndrome MalaCards C4084767 Bothered by vomiting C0025637 Methemoglobinemia HSDN C0008031 Pain chest C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C0036572 Convulsion C0586323 Alcohol withdrawal seizures UMLS C1963281 Vomiting adverse event C0033975 Psychotic disorders HSDN C0028961 Urine output decreased C0040524 Septic toxemia HSDN C0751837 Gait ataxic C1414203 Dws gene HSDN C2237041 Shox gene with short stature C0796272 Brooks syndrome MalaCards C1962972 Proteinuria adverse event C0031511 Pheochromocytoma MalaCards|HSDN|HPO C3274924 Have been coughing C0263662 Disseminated eosinophilic collagen disease HSDN C0151827 Pain eye C0003081 Anisometropia HSDN C4042891 Sleep wake disorders C2347126 Microscopic polyarteritis HSDN C4084767 Bothered by vomiting C0016510 Foot diseases HSDN C3463815 Feel fatigue C0751674 Lymphangioleiomyomatosis MalaCards|HPO C2984058 Have pain C0037361 Olfactory sense HSDN C4020887 Photodysphoria C0162361 Hidrotic ectodermal dysplasia OrphaNet|HPO C0151786 Weakness muscle C0007194 Hypertrophic cardiomyopathy HSDN C3539020 Pelvic pain decreasing in frequency C0010068 Coronary heart disease HSDN C0013390 Cramps menstrual C0406670 Burning vulva HSDN C0015938 Fetal macrosomia C0041107 Trisomy HSDN C0026838 Spasticity muscle C0917796 Optic atrophy, hereditary, leber HSDN C1961131 Cough adverse event C0027831 Neurofibromatosis 1 HSDN C0012569 Double vision C0001418 Adenocarcinoma HSDN C0034150 Skin purpura C0012236 Digeorge syndrome MalaCards|HPO C0038002 Spleen enlargement C1304205 Neutrophilic urticaria MalaCards C0000737 Abdomen pain C0856761 Budd-chiari syndrome OrphaNet|HSDN|HPO|MalaCards C2919142 Short stature adverse event C0023234 Legg-calve-perthes disease OrphaNet|HPO|MalaCards C3641755 Have constipation C0034065 Pulmonary embolism HSDN C2315100 Pediatric failure to thrive C0030779 Pelger-huet anomaly MalaCards|HPO C0036572 Convulsion C0019699 Hiv seropositivity HSDN C0019079 Bloody sputum C0740767 Resp_tract problem UMLS C2096293 Ent surgical result ear vertigo C0013808 Electroconvulsive therapy HSDN C0015300 Ocular proptosis C2940786 Thyroid hormone resistance syndrome HPO C0040264 Ear ringing sound C1881674 Medical device emits smoke HSDN C0231528 Muscle pain generalized C0746883 Febrile neutropenia HSDN C0018991 Paralysis one side of body C0032914 Pre-eclampsia HSDN C0035229 Respiratory function impaired C0158641 Lung, cysts, congenital MalaCards C0042963 Symptoms vomiting C0037361 Olfactory sense HSDN C1963274 Vasculitis adverse event C1304205 Neutrophilic urticaria MalaCards C1549543 Administration method - pain C0206682 Follicular thyroid carcinoma HSDN C0024032 Birth weight subnormal C3280296 Microcephaly-capillary malformation syndrome MalaCards C3665492 Pigmentations C0028945 Oligodendroglioma MalaCards C0413252 Hypothermia due to exposure C1963215 Pneumothorax adverse event HSDN C4085210 Usual severity pain C0004940 Behavioral science HSDN C3815497 Cough C0009240 Cognition HSDN C1963184 Nystagmus adverse event C0393591 Aicardi-goutieres syndrome HPO C2242996 Tingling C0004943 Behcet syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0040124 Thyroglossal duct cyst HSDN C0011175 Deficient fluid volume C3280314 Combined malonic and methylmalonic aciduria MalaCards C0043094 Weight gain C0034088 Pulmonary valve insufficiency HSDN C0022346 Yellow skin C2931787 Intracardiac myxoma MalaCards C0003962 Ascites C3273116 Gallbladder net MalaCards C0023012 Delay language C3150675 Chromosome 15q24 duplication syndrome HPO C0031911 Pigment deposition C0153632 Malig neop oth spec site eye MalaCards C0518090 Frequency of pain question C0003128 Anovulation HSDN C0013404 Respiratory difficulty C1414899 Gaa gene HSDN C0007758 Cerebellar ataxia C0023903 Liver neoplasms HSDN C1260880 Nasal drip C3146259 Stage iv nasopharyngeal carcinoma ajcc v7 UMLS C4049644 Depression C2931859 Acquired cjd MalaCards C4085210 Usual severity pain C0034186 Pyelonephritis HSDN C0033774 Skin pruritus C0041755 Adverse reaction to drug UMLS C0242936 Center pain C0015579 Family characteristics HSDN C0011168 Disorder deglutition C0206138 Crest syndrome OrphaNet|MalaCards C0023012 Delay language C3810200 Short-rib thoracic dysplasia 11 with or without polydactyly MalaCards C2919142 Short stature adverse event C1848864 Thoracic dysplasia-hydrocephalus syndrome OrphaNet|MalaCards C0917816 Deficiency mental C0796279 Carnevale syndrome MalaCards|HPO C0242936 Center pain C0040124 Thyroglossal duct cyst HSDN C0023222 Lower extremity pain musculoskeletal C0011989 Camurati-engelmann syndrome UMLS C0684343 Pseudophakia C0042826 Field visual HSDN C0086437 Joint hypermobility C3698541 Ohdo syndrome, maat-kievit-brunner type MalaCards C0278152 Hemifacial spasms C0085543 Epilepsia partialis continua HSDN C4085211 Pain distress question C0018203 Chronic granulomatous disease HSDN C0041105 Jaw spasm C0010278 Craniosynostosis HSDN C0020673 Hypothermia (central) (local) C0520946 Emotional hypersensitivity HSDN C0042928 Paralysis vocal cord C0031347 Pharyngeal neoplasms HSDN C4084788 Have dizziness C0282507 Heat stress disorders HSDN C0040822 D tremors C0079487 Helicobacter infections HSDN C3641755 Have constipation C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C3641755 Have constipation C1956093 Paris-trousseau thrombocytopenia MalaCards C2032395 Pelvic pain on the left C1000483 Genus anemia HSDN C0030486 Extremity paralysis, lower C0027830 Neurofibroma HSDN C0040822 D tremors C3809824 Parkinson disease 20, early-onset MalaCards|UMLS C1963274 Vasculitis adverse event C0271270 Oculovestibuloauditory syndrome MalaCards C0018991 Paralysis one side of body C0031090 Periodontal diseases HSDN C2237041 Shox gene with short stature C2931643 Madokoro ohdo sonoda syndrome MalaCards C1963087 Constipation adverse event C0037313 Sleep HSDN C0151686 Growth retardation C2675875 Chromosome 2p16.1 p15 deletion syndrome OrphaNet C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0878544 Cardiomyopathies HSDN C4084784 Diarrhea C0025281 Meniere disease HSDN C4085862 Bothered by nausea C0027962 Melanocytic nevus HSDN C4085548 Usual severity dizziness C0003813 Arrhythmia sinus HSDN C0034124 Pupillary disorder C0043253 Trauma blunt HSDN C4084726 Distress cough C0024141 Lupus erythematosus, systemic HSDN C4084769 Vomiting frequency C0042384 Vasculitis HSDN C4084725 Usual severity cough C0206171 Community acquired infections HSDN C3887638 Failure to thrive in infant C0001198 Disease pink HSDN C4084784 Diarrhea C0001815 Primary myelofibrosis HSDN C0039870 Leanness C0036341 Schizophrenia HSDN C0003862 Pain joint C0015806 Femur neck fracture HSDN C0018772 Deafness C0035920 Rubella HSDN C0000737 Abdomen pain C0035439 Rheumatic heart disease HSDN C0424755 Fever symptoms C0243050 Cardiovascular abnormalities HSDN C0011991 Loose stools C0206718 Ganglioneuroblastoma HSDN C0013604 Edematous C0030807 Pemphigus, nos HSDN C0015672 Decreased energy C0085073 Prosthesis-related infection HSDN C0002962 Angina C0035358 Retroperitoneal neoplasm HSDN C0013404 Respiratory difficulty C0206141 Idiopathic hypereosinophilic syndrome HSDN C0015970 Fever unknown origin C0019100 Severe dengue HSDN C0018681 Headache, cephalalgia C3838758 Familial hyperaldosteronism type 3 MalaCards C0027796 Neuralgias C0154743 Neuropathy ulnar HSDN C0349489 Fetal hypoxia C0007222 Cardiovascular diseases HSDN C0022346 Yellow skin C0268314 Cholestasis-edema syndrome, norwegian type OrphaNet|UMLS|MalaCards C0039870 Leanness C0007134 Renal cell carcinoma HSDN C0009806 Constipate C0021361 Female infertility HSDN C1963137 Hydrocephalus adverse event C0206663 Neuroectodermal tumor, primitive MalaCards C0270948 Neurogenic muscular atrophy C3150667 Microcephaly, seizures, and developmental delay MalaCards|HPO C4084773 Bothered by weight gain C3541306 Plasmodium measurement HSDN C0018681 Headache, cephalalgia C3827253 Classical glioblastoma UMLS C0036572 Convulsion C0796022 Lujan fryns syndrome HPO|UMLS C1963274 Vasculitis adverse event C0549143 Pulmonary renal syndrome MalaCards C1963249 Tinnitus adverse event C0037744 Perceptual spatial orientation HSDN C0019825 Voice hoarseness C0022593 Keratosis HSDN C0086565 Liver function abnormal C0242292 Mccune-albright syndrome HPO C0036572 Convulsion C2030274 Heavy bleeding between periods HSDN C0004134 Dyssynergia C2931082 Familial apoceruloplasmin deficiency MalaCards C0851578 Disorder sleep C0030567 Parkinson disease MalaCards C0013604 Edematous C2350350 Ventilator induced lung injury HSDN C4084768 Usual severity vomiting C0018482 Haemophilus infections HSDN C3463815 Feel fatigue C0025284 Meningeal neoplasms HSDN C0151311 Cranial nerve palsy C0265246 Townes syndrome MalaCards|HPO C0020672 Body temperature decreased C0030286 Pancreatic diseases HSDN C2984058 Have pain C2963140 Arteriovenous fistula in use with two needles HSDN C1963252 Tremor adverse event C0009946 Conversion disorder HSDN C3541349 Syncope C0393911 Pure autonomic failure MalaCards|HSDN C3274924 Have been coughing C0041327 Tuberculosis, pulmonary MalaCards C0031911 Pigment deposition C1176475 Ductal carcinoma MalaCards C0000737 Abdomen pain C0278804 Adenocarcinoma of duodenum UMLS C0243026 Generalized infection C0155866 Inhalational anthrax OrphaNet|MalaCards C0413252 Hypothermia due to exposure C0243026 Sepsis HSDN C3641756 Have diarrhea C0037198 Sinus thrombosis, intracranial HSDN C0878773 Bladder hyperactive C1999266 Depression adverse event HSDN C1963170 Hypothermia adverse event C0020659 Hypothalamic neoplasms HSDN C2024878 Cardiovascular surgery result: dyspnea C0340231 Tracheobronchomalacia HSDN C2984057 Have nausea C2240378 Cleft palate on exam HSDN C0027796 Neuralgias C0040456 Tooth impaction HSDN C0039070 Collapse fleeting C0586323 Alcohol withdrawal seizures UMLS C2024893 Cardiovascular surgery result: fatigue C0023827 Liposarcoma MalaCards C0043094 Weight gain C0027902 Neuropsychological diagnosis HSDN C0349588 Stature short C2931588 Gemss syndrome OrphaNet|HPO|MalaCards C0039231 Heartbeats increased C2931689 Dystrophia myotonica 2 MalaCards|HPO C2203646 Jaundice C3501835 Alpha-1-antitrypsin deficiency, autosomal recessive OrphaNet|HPO C1963065 Apnea adverse event C0020488 Hypernatremia HSDN C0151827 Pain eye C0024437 Macular degeneration HSDN C0010200 Cough symptom C0009324 Ulcerative colitis HSDN C0041105 Jaw spasm C0017675 Glossitis HSDN C0036396 Sciatica C0030793 Pelvis tumor HSDN C2237041 Shox gene with short stature C1876175 Ataxia-telangiectasia variant MalaCards|HPO C0023530 Leukopenia C0242380 Endocarditis, atypical, verrucous MalaCards C0009421 Comatose C0010481 Cushing syndrome HSDN C0041105 Jaw spasm C0038395 Streptococcal infections HSDN C1963071 Back pain adverse event C0029464 Osteosclerosis HSDN C0013604 Edematous C0022410 Joint instability HSDN C2029884 Hearing loss by exam C0011875 Diabetic angiopathies HSDN C1963170 Hypothermia adverse event C0014335 Enteritis HSDN C0242936 Center pain C0524851 Neurodegenerative disorders HSDN C0242936 Center pain C0016665 Fracture, nos with nonunion HSDN C3274924 Have been coughing C0700095 Central neuroblastoma HSDN C0015676 Mental fatigue C0812393 Cancer patients and suicide and depression HSDN C4085317 Diarrhea frequency C0027439 Nasopharyngeal neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0751799 Brain hemorrhage, traumatic HSDN C4085317 Diarrhea frequency C0853698 Lymphocytes increased HSDN C1549543 Administration method - pain C0035258 Restless legs syndrome HSDN C1145670 Failure respiratory C3146222 Idiopathic aortitis MalaCards C0231835 Respiration rate increased C0268579 Propionic acidemia HPO C0557874 Global developmental delay C3809006 Cardiofaciocutaneous syndrome 3 MalaCards C0242936 Center pain C0004114 Astrocytoma HSDN C1963154 Renal failure adverse event C3665382 2,8-dihydroxyadenine urolithiasis MalaCards C4084766 Vomiting C0267494 Chilaiditi's syndrome HSDN C4084784 Diarrhea C0032002 Pituitary diseases HSDN C0150045 Urinary incontinence urge C0032787 Postoperative complications HSDN C0010200 Cough symptom C0085167 Granular cell tumor HSDN C1279888 Proteinuria of undiagnosed cause C0038220 Status epilepticus HSDN C0700078 Deep tendon reflex decrease C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C1963281 Vomiting adverse event C0342792 Succinyl-coa:3-oxoacid coa transferase deficiency HPO C0424755 Fever symptoms C0026640 Mouth neoplasms HSDN C0349588 Stature short C2675228 Ciliary dyskinesia, primary, 12 MalaCards|HPO C2362324 Pediatric obesity C2713543 Biofeedback eeg HSDN C0017181 Gastrointestinal bleed C1847319 Paraganglioma and gastric stromal sarcoma OrphaNet|HPO|MalaCards C0026826 High muscle tone C0432217 Wolcott-rallison syndrome HPO C0007758 Cerebellar ataxia C0023240 Legionellosis MalaCards C0024031 Back pain lower back C0030305 Pancreatitis HSDN C0041657 Consciousness loss C0242891 Injuries teeth HSDN C0426579 Anorexia symptom C0151467 Addisonian crisis OrphaNet|MalaCards C3274924 Have been coughing C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C1963281 Vomiting adverse event C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency HPO C4084767 Bothered by vomiting C0020437 Hypercalcemia HSDN C3641755 Have constipation C0007097 Carcinomas HSDN C0270948 Neurogenic muscular atrophy C4015360 Nemaline myopathy 10 MalaCards C0013421 Dystonia C3179455 Niemann-pick disease, type c1 MalaCards|HPO C4084768 Usual severity vomiting C0026936 Mycoplasma infections HSDN C0042798 Vision dim C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0020672 Body temperature decreased C0008354 Cholera HSDN C2025995 Cellulitis C0221026 X-linked agammaglobulinemia OrphaNet|HPO C0000737 Abdomen pain C1318541 Sertoli-leydig cell tumor of intermediate differentiation HSDN C0018524 Hallucinate C0021819 Psychological interview HSDN C0026838 Spasticity muscle C0002792 Anaphylaxis HSDN C1579931 Depressed - symptom C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C4085317 Diarrhea frequency C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C1963252 Tremor adverse event C1839576 Optic atrophy 2 (disorder) MalaCards C1279888 Proteinuria of undiagnosed cause C1619700 Renal adysplasia MalaCards|HPO C0000737 Abdomen pain C0406608 Pelvic lipomatosis UMLS C0037317 Sleep disturbance C0282644 Smith-lemli-opitz syndrome, type ii MalaCards C0018681 Headache, cephalalgia C0019069 Hemophilia a HSDN C0007758 Cerebellar ataxia C0013502 Echinococcosis HSDN C0036572 Convulsion C2004491 Cicatrix HSDN C0271052 Retinal edema, peripheral C0242420 Edema retinal UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0026272 Mixed connective tissue disease HSDN C0020538 Hbp C0268322 Chester-type porphyria HPO C0019521 Hiccoughs C0032290 Aspiration pneumonia HSDN C0020538 Hbp C1833699 Osteopoikilosis, isolated MalaCards C0242936 Center pain C0034012 Delayed puberty HSDN C0043094 Weight gain C0032285 Pneumonia HSDN C0413252 Hypothermia due to exposure C0013928 Fat embolism HSDN C4085317 Diarrhea frequency C0040127 Thyroid crisis HSDN C2024893 Cardiovascular surgery result: fatigue C0011265 Presenile dementia HSDN C0427190 Ataxia, truncal C0024408 Machado-joseph disease MalaCards|HPO|UMLS C1856661 Cornea cloudy C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards C0151786 Weakness muscle C0206366 Ossification of posterior longitudinal ligament HSDN C0009676 Confusion state C0007820 Cerebrovascular disorders HSDN C4084726 Distress cough C0019621 Histiocytosis, langerhans-cell HSDN C0431949 Congenital clicking hip C0265615 Hip deformity congenital nos UMLS C1384666 Decreased hearing C2931557 Chromosome 4 short arm deletion MalaCards C0040822 D tremors C0334123 Histiocytosis, lipoid MalaCards C4084767 Bothered by vomiting C0342443 Adrenal cushing's syndrome HSDN C0004134 Dyssynergia C0036341 Schizophrenia HSDN C2024878 Cardiovascular surgery result: dyspnea C0039128 Syphilis HSDN C0040822 D tremors C3889636 Spinocerebellar ataxia 37 MalaCards C0003910 Articulation disorder C0033199 Proactive inhibition HSDN C1557397 Adverse event associated with pain C0037198 Sinus thrombosis, intracranial HSDN C0013604 Edematous C0017181 Gastrointestinal hemorrhage HSDN C3815497 Cough C0018674 Head trauma HSDN C0557874 Global developmental delay C0265221 Walker-warburg congenital muscular dystrophy MalaCards|HPO C4084766 Vomiting C0000735 Abdominal neoplasms HSDN C0242936 Center pain C0524988 Schnitzler syndrome HSDN C0344315 Mood depressed C3665349 Secondary hypothyroidism OrphaNet C1000483 Genus anemia C1335398 Gastric peutz-jeghers polyp MalaCards C0851578 Disorder sleep C0563150 Catastrophization HSDN C0026821 Cramp C2945560 Hemolytic HSDN C0151686 Growth retardation C2673610 Jeb-i MalaCards C0013390 Cramps menstrual C0023533 Vaginal discharge white HSDN C4085211 Pain distress question C0013922 Embolism HSDN C3887638 Failure to thrive in infant C0432443 Deletion of long arm of chromosome 18 MalaCards C1069915 Vertigo C0346303 Thyrotroph adenoma MalaCards C0027497 Queasy C0043121 Wernicke encephalopathy HSDN C2984058 Have pain C0000821 Threatened abortion HSDN C0235263 Congestion conjunctival C0009774 Conjunctivitis viral MalaCards C2203646 Jaundice C0023794 Lipoidosis HSDN C0231835 Respiration rate increased C0010383 Crowd HSDN C1962972 Proteinuria adverse event C0014761 Erythroblastosis, fetal HSDN C0038990 Sweats C3150809 Ectodermal dysplasia-syndactyly syndrome 2 MalaCards C0030193 Sense of pain C1963211 Pericarditis adverse event HSDN C1963249 Tinnitus adverse event C3244301 Coverage level - family HSDN C2919142 Short stature adverse event C2931889 Oral-facial-digital syndrome, type 2 MalaCards C0042024 Urine incontinence C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0019079 Bloody sputum C0011854 Diabetes mellitus, insulin-dependent HSDN C0015469 Facial paralysis C1853554 Radiation induced meningioma MalaCards C3539891 Pelvic pain to the rear C1961100 Erectile dysfunction adverse event HSDN C0024032 Birth weight subnormal C0342784 Pearson's marrow-pancreas syndrome MalaCards C0522224 Palsied C0039494 Temporomandibular joint disorders HSDN C1963184 Nystagmus adverse event C1833321 Chorioretinal atrophy, progressive bifocal OrphaNet|MalaCards C1549543 Administration method - pain C0585442 Osteosarcoma of bone HSDN C0013404 Respiratory difficulty C0854985 Adenocarcinoma of lung, stage i UMLS C0242936 Center pain C0026718 Mucormycosis HSDN C0413252 Hypothermia due to exposure C0085183 Neoplasms, second primary HSDN C3539893 Pelvic pain occurs with intercourse C0022661 Kidney failure, chronic HSDN C4084802 Usual severity diarrhea C0302280 Adrenogenital syndrome HSDN C0009460 Communication impairment C2713543 Biofeedback eeg HSDN C0349588 Stature short C1275079 Acps iii MalaCards C4084773 Bothered by weight gain C0025521 Inborn errors of metabolism HSDN C0424755 Fever symptoms C1306220 Fort bragg fever MalaCards C0026603 Motion sickness C0003811 Cardiac arrhythmia HSDN C0020580 Decreased sensation C0034885 Rectal neoplasms HSDN C0011206 Delirium acute C1962976 Ventricular fibrillation adverse event HSDN C0018991 Paralysis one side of body C1263846 Attention deficit hyperactivity disorder HSDN C0085636 Light sensitivity C1562894 Thiel-behnke corneal dystrophy MalaCards|HPO C0036659 Sensation disorder C0030445 Obstetric paralysis HSDN C1069915 Vertigo C0034065 Pulmonary embolism HSDN C0030193 Sense of pain C0334552 Malignant giant cell tumor of bone UMLS C0004604 Pain back C0031212 Personality disorders HSDN C4085548 Usual severity dizziness C0011570 Mental depression HSDN C4084788 Have dizziness C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) MalaCards C1963071 Back pain adverse event C0003509 Aortitis, nos HSDN C0013404 Respiratory difficulty C1709570 Pleural biphasic mesothelioma UMLS C4085642 Level of joint stiffness C1835614 Hereditary hyperexplexia MalaCards C1962972 Proteinuria adverse event C0029408 Degenerative polyarthritis HSDN C0018772 Deafness C0024761 Communication, manual HSDN C4085317 Diarrhea frequency C0001418 Adenocarcinoma HSDN C0024031 Back pain lower back C0038941 Incisional infection HSDN C0018681 Headache, cephalalgia C0162869 Aneurysm, ruptured HSDN C0011168 Disorder deglutition C1833373 Inclusion body myopathy, autosomal recessive MalaCards C0009806 Constipate C0039614 Tetanus HSDN C2919142 Short stature adverse event C0043346 Xeroderma pigmentosum MalaCards|HPO C0587047 Mass of trunk C0269220 Cyst vulva UMLS C0270846 Astatic seizure C3810400 Epileptic encephalopathy, early infantile, 19 MalaCards C0151825 Ostalgia C0025239 Melorheostosis MalaCards C0011991 Loose stools C0018944 Hematoma HSDN C0575081 Abnormal gait C3683846 Chromosome 17p deletion syndrome MalaCards C0240859 Rales, basilar C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C4084802 Usual severity diarrhea C2117118 X-ray of toe: deformity contracture HSDN C0020672 Body temperature decreased C1720777 Functional laterality HSDN C0000727 Abdomen acute C0518450 Spinal fractures HSDN C0036572 Convulsion C0010273 Craniofacial dysostosis MalaCards|HPO C0018991 Paralysis one side of body C0027947 Neutropenia HSDN C0746674 Muscle weakness generalized C1846344 Bartter syndrome, type 3, with hypocalciuria HPO C1963137 Hydrocephalus adverse event C2674574 Aortic aneurysm, familial thoracic 3 MalaCards C3665492 Pigmentations C1368295 Malignant basal cell tumor MalaCards C0003811 Cardiac rhythm disturbance C3538999 Dystonia 23 MalaCards C1557397 Adverse event associated with pain C1962976 Ventricular fibrillation adverse event HSDN C0557874 Global developmental delay C4014488 Pontocerebellar hypoplasia, type 2e MalaCards C4085317 Diarrhea frequency C0039336 Gustatory sense HSDN C4085317 Diarrhea frequency C0014179 Endometritis HSDN C0018777 Deafness, conductive C0206586 Endolymphatic hydrops HSDN C0004134 Dyssynergia C1836841 Ceroid lipofuscinosis, neuronal, 9 (disorder) MalaCards|UMLS C2984058 Have pain C0017570 Gingival neoplasms HSDN C0221263 Cafe au lait spot C0009447 Common variable immunodeficiency HSDN C1963091 Diarrhea adverse event C1829813 Malonic acidemia MalaCards C4085549 Dizziness C0024115 Lung diseases HSDN C4085211 Pain distress question C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C4084802 Usual severity diarrhea C3149237 Men1 somatic mutations HPO C0454644 Delayed language development C0270972 Cornelia de lange syndrome HPO C0016199 Pain flank C0032962 Pregnancy complications HSDN C0034124 Pupillary disorder C1963138 Hypertension adverse event HSDN C0241165 Skin thickening C1510415 Osteosclerotic myeloma MalaCards C1384666 Decreased hearing C0021400 Influenza HSDN C0020580 Decreased sensation C0149940 Sciatic neuropathy HSDN C0747556 Pharyngitis recurrent C1304456 Congo hemorrhagic fever MalaCards C0026838 Spasticity muscle C1858804 Cerebellar ataxia, deafness, and narcolepsy HPO C2315100 Pediatric failure to thrive C3810055 Combined oxidative phosphorylation deficiency 19 MalaCards C2242996 Tingling C0009450 Disease caused by microorganism HSDN C0751295 Memory loss or impairment C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C1145670 Failure respiratory C2930798 Alexanders leukodystrophy MalaCards C0007758 Cerebellar ataxia C3887678 Cpnet MalaCards C0000727 Abdomen acute C0009404 Colorectal neoplasms HSDN C2203646 Jaundice C0004943 Behcet syndrome HSDN C0314719 Dry eyes C3665609 Conjunctival xerosis UMLS C0042571 Vertigo subjective C0517555 Venous thrombosis after immobility HSDN C3641756 Have diarrhea C0006818 Campylobacter infection DiseaseOntology C0042755 Virilisation C1963059 Adrenal insufficiency adverse event HSDN C1963091 Diarrhea adverse event C1527429 Increased blood npn HSDN C1963281 Vomiting adverse event C0162565 Acute intermittent porphyria MalaCards|HSDN|HPO C4084784 Diarrhea C0009917 Contracture HSDN C0009676 Confusion state C0011849 Diabetes mellitus HSDN C0221752 Rbc urine C1851986 Dyschondrosteosis and nephritis OrphaNet|MalaCards C1963091 Diarrhea adverse event C0018965 Hematuria HSDN C1384666 Decreased hearing C0311468 Increased bilirubin level (finding) HSDN C0034150 Skin purpura C0035229 Respiratory insufficiency HSDN C3641755 Have constipation C0035412 Rhabdomyosarcoma HSDN C0003467 Angst C0033800 Pseudoglioma MalaCards C2984057 Have nausea C0033871 Psychiatric status rating scales HSDN C0042510 Fibrillation paroxysmal vent C3501852 Long qt syndrome 2/3 MalaCards C3815497 Cough C0038661 Suicide HSDN C2315100 Pediatric failure to thrive C0011981 Diaphragmatic eventration HSDN C0036572 Convulsion C0037354 Smallpox HSDN C4084769 Vomiting frequency C0027809 Neurilemmoma HSDN C0030554 Abnormal sensation C0034494 Rabies (disorder) OrphaNet|MalaCards C4084766 Vomiting C1553188 Hemolysis - observation HSDN C1971624 Appetite absent C1000483 Genus anemia HSDN C4084776 Weight loss C0006434 Burn injury HSDN C0035232 Diaphragmatic paralysis C0027888 Hereditary motor and sensory neuropathies HSDN C4084774 Have weight loss C0872315 Communicable diseases emerging HSDN C0237326 Defecation pain C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0018772 Deafness C0017653 Glomus tumor HSDN C4085661 Usual severity nausea C1546847 Entity name part type - family HSDN C0002622 Amnesias C0042830 Perception visual HSDN C0424755 Fever symptoms C0001883 Airway obstruction HSDN C2911645 Weight loss adverse event C0004275 Attitude health HSDN C0010520 Skin cyanosis C0013927 Embolism, amniotic fluid HSDN C1860844 Sparse, thin hair C1274795 Urban schosser spohn syndrome OrphaNet|MalaCards C0242936 Center pain C0003950 Ascariasis HSDN C0018772 Deafness C0027407 Narcotherapy HSDN C0015672 Decreased energy C3163620 Hypotension adverse event HSDN C0518090 Frequency of pain question C0037413 Social dominance HSDN C0241057 Skin burning sensation C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C3714644 Thymus neoplasms MalaCards|HSDN C0018926 Emesis bloody C0013298 Duodenitis HSDN C0031911 Pigment deposition C0206696 Carcinoma, signet ring cell MalaCards C0042963 Symptoms vomiting C0021603 Sleep initiation and maintenance disorders HSDN C2984058 Have pain C0311389 Nonspecific urethritis HSDN C3539892 Pelvic pain in front C0020550 Hyperthyroidism HSDN C0242936 Center pain C2931384 Moyamoya disease 1 HSDN C4084725 Usual severity cough C0039978 Thoracic diseases HSDN C0043144 Wheeze C0264409 Allergic asthma with stated cause UMLS C0019825 Voice hoarseness C0236969 Substance-related disorders HSDN C3541349 Syncope C0520946 Emotional hypersensitivity HSDN C0518090 Frequency of pain question C2350530 Bronchopulmonary aspergillosis HSDN C0917801 Sleep disorder insomnia C0581874 Late insomnia UMLS C0413252 Hypothermia due to exposure C0026266 Mitral valve insufficiency HSDN C0013404 Respiratory difficulty C2939462 Immunoglobulin deposition disease MalaCards C0009421 Comatose C0032326 Pneumothorax HSDN C3146279 Coma C0021832 Intestinal diseases, parasitic HSDN C2029884 Hearing loss by exam C0262655 Recurrent urinary tract infection HSDN C2984057 Have nausea C0038013 Ankylosing spondylitis HSDN C0151889 Reflexes tendon increased C1835896 Spastic paraplegia 30, autosomal recessive (disorder) MalaCards|HPO C0028738 Nystagmus C1847352 Polymicrogyria, bilateral frontoparietal MalaCards|HPO C0150055 Pain chronic C0262655 Recurrent urinary tract infection HSDN C4084727 Cough frequency C0024525 Malacoplakia MalaCards C3539022 Pelvic pain decreasing in severity C0009373 Colonic diseases HSDN C0030193 Sense of pain C1336300 Stage ii carcinoma of nasal cavity UMLS C0020578 Hyperventilate C0242992 Multiple chemical sensitivity HSDN C0027498 Nausea vomiting C0086181 Intravenous drug abuse UMLS C2984057 Have nausea C0206245 Amyloid neuropathies, familial HSDN C0036572 Convulsion C0280475 Childhood oligodendrogliomas UMLS C0027497 Queasy C0036916 Sexually transmitted diseases HSDN C0015469 Facial paralysis C0039494 Temporomandibular joint disorders HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027947 Neutropenia HSDN C0000727 Abdomen acute C0014852 Esophageal diseases HSDN C0030193 Sense of pain C0027429 Nasal obstruction present finding HSDN C0234428 Consciousness disturbance C2197983 Acute reaction to stress with disturbance of consciousness UMLS C4084724 Usual severity constipation C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C4085211 Pain distress question C0031039 Effusion pericardial HSDN C0036572 Convulsion C1865926 Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) UMLS C2024878 Cardiovascular surgery result: dyspnea C1868684 Ear, patella, short stature syndrome MalaCards C0234146 Absent reflex C0205710 Alpers syndrome (disorder) OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0085437 Meningitis, bacterial HSDN C1069915 Vertigo C0030353 Papilledema HSDN C0023380 Lethargy C0270858 Abdominal migraines MalaCards C0027796 Neuralgias C0038525 Subarachnoid hemorrhage HSDN C4084724 Usual severity constipation C0007095 Carcinoid tumor HSDN C1963249 Tinnitus adverse event C0271270 Oculovestibuloauditory syndrome MalaCards C0019209 Large liver C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0152942 Enteric tularemia nos DiseaseOntology|MalaCards C0413252 Hypothermia due to exposure C0151516 Thyroid hypoplasia HPO C3829611 Nausea frequency C0085293 Hepatitis e MalaCards C4084773 Bothered by weight gain C0001314 Acute disease HSDN C0000737 Abdomen pain C2981380 Stage iiia small intestinal cancer UMLS C0026838 Spasticity muscle C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0011206 Delirium acute C0220847 C hepatitis virus HSDN C0085636 Light sensitivity C1835897 Retinal cone dystrophy 3b MalaCards|HPO|UMLS C0007166 Cardiac output decreased C0162526 Aids-related opportunistic infections HSDN C4085211 Pain distress question C0015652 Fascioliasis HSDN C0020305 Fetal edema C0036868 Sex chromosome aberrations HSDN C0018926 Emesis bloody C0003950 Ascariasis HSDN C4042891 Sleep wake disorders C0001175 Acquired immunodeficiency syndrome HSDN C0042571 Vertigo subjective C0041582 Ulcer HSDN C2919142 Short stature adverse event C1955934 Trichothiodystrophy syndromes MalaCards C1384666 Decreased hearing C3683846 Chromosome 17p deletion syndrome MalaCards C4085211 Pain distress question C0019880 Homocystinuria HSDN C3539896 Pelvic pain occurs with urination C1000483 Genus anemia HSDN C3146279 Coma C1963064 Anxiety adverse event HSDN C0018681 Headache, cephalalgia C0016627 Avian influenza HSDN C0002962 Angina C0025063 Mediastinal neoplasms HSDN C4084723 Constipation C2940785 Hypothyroidism, congenital, nongoitrous, 3 MalaCards C0040485 Wryneck C0302148 Blood clot HSDN C0424755 Fever symptoms C0026229 Mite infestation HSDN C0231218 Malaise generalized C1516490 Cholangiolocellular carcinoma UMLS C0034933 Abnormal reflexes C0234194 Nociception HSDN C0034150 Skin purpura C0282548 Leukostasis HSDN C0233565 Bradykinesia C1839040 Leber optic atrophy and dystonia UMLS C0231218 Malaise generalized C3273134 Extrahepatic bile duct cystadenocarcinoma UMLS C2911645 Weight loss adverse event C0032344 Poisoning aspects HSDN C2242996 Tingling C0027663 Neoplasms, multiple primary HSDN C0022568 Inflammation corneal C0021171 Bloch sulzberger syndrome MalaCards|HPO C0007758 Cerebellar ataxia C0033817 Pseudomonas infections HSDN C1557397 Adverse event associated with pain C0152177 Trigeminal neuropathy HSDN C1963087 Constipation adverse event C0019557 Hip fx HSDN C4085211 Pain distress question C0018081 Gonorrhea HSDN C0030552 Paralysis partial C0751877 Hereditary central nervous system demyelinating diseases HSDN C1963252 Tremor adverse event C1847640 Kufor-rakeb syndrome MalaCards C2315100 Pediatric failure to thrive C0751918 Cockayne pelizaeus merzbacher disease MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0270857 Epilepsy, reflex HSDN C0262527 Intermittent abdominal pain C3809250 Estrogen resistance MalaCards C2984057 Have nausea C0017168 Gastroesophageal reflux disease HSDN C0018681 Headache, cephalalgia C0220847 C hepatitis virus HSDN C0033777 Genital pruritus C1290866 Disease of pelvis UMLS C1549543 Administration method - pain C0235833 Congenital diaphragmatic hernia HSDN C0024031 Back pain lower back C0007273 Carotid artery diseases HSDN C1963071 Back pain adverse event C0011175 Dehydration HSDN C1384666 Decreased hearing C0796279 Carnevale syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C3203360 Suppuration HSDN C0424755 Fever symptoms C0032584 Polyps HSDN C0221170 Stiffness muscle C3810160 Spastic paraplegia 72, autosomal recessive MalaCards|UMLS C0518090 Frequency of pain question C0028431 Acquired nasal deformities HSDN C0234512 Prosopagnosia C0042826 Field visual HSDN C1962972 Proteinuria adverse event C0027059 Myocarditis HSDN C1963252 Tremor adverse event C2015933 Outcomes otolaryngology hearing HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1762616 Meningioma, benign, no icd-o subtype HSDN C0162298 Stiffness joints C1838162 Mesomelia-synostoses syndrome MalaCards C1557397 Adverse event associated with pain C0221391 Melanosis coli HSDN C0426579 Anorexia symptom C0023281 Leishmaniasis MalaCards C1971624 Appetite absent C0036202 Sarcoidosis MalaCards C4084802 Usual severity diarrhea C0043167 Pertussis HSDN C3146279 Coma C3813607 Infantile gastroesophageal reflux HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027902 Neuropsychological diagnosis HSDN C4085661 Usual severity nausea C0270858 Abdominal migraines MalaCards C1069915 Vertigo C0456892 Csf low pressure HSDN C0042571 Vertigo subjective C0022650 Kidney calculi HSDN C0518090 Frequency of pain question C0282193 Iron overload HSDN C0012833 Dizzy C3887532 Ulceration HSDN C0522224 Palsied C0037006 Shoulder fracture HSDN C0151786 Weakness muscle C0023772 Lipid metabolism, inborn errors HSDN C0036659 Sensation disorder C0339527 Leber congenital amaurosis HSDN C0033774 Skin pruritus C1335979 Extrahepatic bile duct small cell nec UMLS C1963184 Nystagmus adverse event C2745959 Spondyloepiphyseal dysplasia, congenita HPO C0013404 Respiratory difficulty C4225360 Epileptic encephalopathy, early infantile, 30 UMLS C1963184 Nystagmus adverse event C0268514 Urocanase deficiency MalaCards|HPO C0242936 Center pain C0517960 Neurological status: consciousness HSDN C3274920 Have shortness of breath question C0004096 Asthma DiseaseOntology|MalaCards C1549543 Administration method - pain C0206721 Inverted papilloma HSDN C0003811 Cardiac rhythm disturbance C4015447 Combined oxidative phosphorylation deficiency 23 MalaCards C0018991 Paralysis one side of body C0009953 Convulsive therapy HSDN C0398650 Idiopathic thrombocytopenia purpura C0677607 Hashimoto disease HSDN C4084775 Usual severity weight loss C0162832 Apc HSDN C1557397 Adverse event associated with pain C3714535 Malocclusion, angle class ii HSDN C4084802 Usual severity diarrhea C0238154 Epidural hematoma HSDN C4084802 Usual severity diarrhea C0334299 Carcinoid tumor no icd-o subtype HSDN C0241210 Speaking delay C3550904 Epileptic encephalopathy, early infantile, 36 MalaCards C0018681 Headache, cephalalgia C0014121 Bacterial endocarditis HSDN C4085548 Usual severity dizziness C0033871 Psychiatric status rating scales HSDN C0242936 Center pain C0017920 Glycogen storage disease type i HSDN C0262527 Intermittent abdominal pain C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C0021359 Infertility C3809634 Ciliary dyskinesia, primary, 24 MalaCards C0030554 Abnormal sensation C0700327 Clinical findings relating to memory HSDN C4084767 Bothered by vomiting C0023487 Acute promyelocytic leukemia HSDN C1971624 Appetite absent C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C3274924 Have been coughing C3714644 Thymus neoplasms OrphaNet|MalaCards C0024031 Back pain lower back C3813607 Infantile gastroesophageal reflux HSDN C3146279 Coma C0029408 Degenerative polyarthritis HSDN C0024031 Back pain lower back C0018552 Hamartoma HSDN C2315100 Pediatric failure to thrive C0003886 Arthrogryposis HSDN C3539889 Pelvic pain increasing in severity C0009375 Colonic neoplasms HSDN C4084788 Have dizziness C1963235 Sick sinus syndrome adverse event HSDN C0018784 Deafness sensorineural C0007570 Celiac disease HSDN C0518090 Frequency of pain question C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C0038990 Sweats C0017075 Ganglioneuroma MalaCards C0151686 Growth retardation C0268581 Holocarboxylase synthetase deficiency OrphaNet|HPO|MalaCards C0034150 Skin purpura C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0019209 Large liver C0086651 Mucopolysaccharidosis, mps-iv-a HPO C4084775 Usual severity weight loss C0001807 Aggressive behavior HSDN C2073625 X-ray of chest: pleural effusion C0265492 Anomaly of chromosome pair ring 22 syndrome MalaCards C3815497 Cough C3179093 Injuries, laryngeal nerve HSDN C0012569 Double vision C2937421 Prostatic hyperplasia HSDN C3815497 Cough C0010340 Critical illness HSDN C1971624 Appetite absent C0030567 Parkinson disease HSDN C0028738 Nystagmus C1568249 Usher syndrome, type ii MalaCards|HPO C0015970 Fever unknown origin C0079731 B-cell lymphomas HSDN C0016382 Cutaneous vascular engorgement C0406557 Poikiloderma of kindler OrphaNet|HPO|MalaCards C0011991 Loose stools C0034362 Q fever HSDN C1963184 Nystagmus adverse event C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards|HPO C0019079 Bloody sputum C0314657 Genetic predisposition HSDN C4084723 Constipation C0033348 Language program HSDN C0026838 Spasticity muscle C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C2242996 Tingling C0162671 Melas syndrome MalaCards|HPO C1549543 Administration method - pain C0041311 Tuberculosis, female genital HSDN C0042024 Urine incontinence C0042258 Vaginal neoplasms HSDN C4085211 Pain distress question C1009209 Tinea HSDN C0000731 Abdomen distention C2931743 Lactate dehydrogenase deficiency type a MalaCards C0038002 Spleen enlargement C0268151 Classical galactosemia MalaCards C2203646 Jaundice C0043410 Pseudotuberculosis HSDN C1549543 Administration method - pain C0013928 Fat embolism HSDN C1963071 Back pain adverse event C3244301 Coverage level - family HSDN C0000737 Abdomen pain C1333860 Grade 2 colorectal adenocarcinoma UMLS C0151827 Pain eye C3814530 Skin vesicle HSDN C0751837 Gait ataxic C0752352 Muscular disorders, atrophic HSDN C0022346 Yellow skin C0042373 Vascular diseases HSDN C0042963 Symptoms vomiting C0014866 Esophageal stenosis HSDN C0038990 Sweats C4053908 Late onset tylosis MalaCards C0015230 Exanthem C0004058 Aspirin allergy UMLS C4085317 Diarrhea frequency C0004589 B. anthracis HSDN C0042571 Vertigo subjective C0085541 Epilepsy, frontal lobe HSDN C0015672 Decreased energy C1299919 Enteric coccidiosis HSDN C1963093 Dizziness adverse event C1565489 Renal insufficiency HSDN C0002962 Angina C0086543 Cataract nos HSDN C0012569 Double vision C0022906 Lacrimal duct obstruction HSDN C0005779 Clotting C0268151 Classical galactosemia MalaCards C3539889 Pelvic pain increasing in severity C0007867 Cervix diseases HSDN C1549543 Administration method - pain C0011389 Dental plaque HSDN C1549543 Administration method - pain C0042063 Urogenital abnormalities HSDN C3541349 Syncope C0037313 Sleep HSDN C4084723 Constipation C2004491 Cicatrix HSDN C0003862 Pain joint C0040034 Thrombocytopenia HSDN C0030193 Sense of pain C0026893 Myalgia and myositis unspecified UMLS C0036572 Convulsion C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C0013421 Dystonia C3809824 Parkinson disease 20, early-onset MalaCards C3641756 Have diarrhea C0023420 Mouse leukemia l1210 HSDN C3829611 Nausea frequency C0032460 Polycystic ovary syndrome HSDN C0008031 Pain chest C0007222 Cardiovascular diseases HSDN|UMLS C0011991 Loose stools C1334297 Delta cell tumor of jejunum UMLS C0030552 Paralysis partial C3888102 Frontotemporal dementia with motor neuron disease MalaCards C0242936 Center pain C0005426 Biliary tract neoplasm HSDN C4084726 Distress cough C0014836 Escherichia coli infections HSDN C3146279 Coma C0038579 Substance abuse, intravenous HSDN C1549543 Administration method - pain C0034884 Rectal fistula HSDN C4084806 Lack of appetite C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C1963087 Constipation adverse event C0027819 Neuroblastoma HSDN C3146279 Coma C0036946 Sheep--diseases HSDN C0042024 Urine incontinence C2931356 Spastic paraplegia type 5a, recessive MalaCards C0349588 Stature short C3151609 Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals HPO C0030552 Paralysis partial C0015480 Disorder factitious HSDN C0020578 Hyperventilate C0022116 Ischemia HSDN C1384666 Decreased hearing C2984572 Malaria pathway HSDN C0009806 Constipate C0854782 Stage ii rectosigmoid cancer UMLS C3641755 Have constipation C0007131 Non-small cell lung carcinoma HSDN C1963087 Constipation adverse event C1704272 Benign prostatic hyperplasia HSDN C0221170 Stiffness muscle C2931743 Lactate dehydrogenase deficiency type a MalaCards|UMLS C0013604 Edematous C0014733 Erysipelas HSDN C0007166 Cardiac output decreased C0520680 Sleep apnea, central HSDN C2203646 Jaundice C0149520 Acute cholecystitis HSDN C0030193 Sense of pain C0010631 Cystadenocarcinoma HSDN C3887638 Failure to thrive in infant C0019209 Hepatomegaly HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0036980 Shock, cardiogenic HSDN C0013404 Respiratory difficulty C0026636 Mouth diseases HSDN C1963091 Diarrhea adverse event C0023493 Adult t-cell lymphoma/leukemia HSDN C2919142 Short stature adverse event C1843042 Craniolenticulosutural dysplasia OrphaNet|HPO|MalaCards C4085222 Nausea C0867389 Chronic graft-versus-host disease MalaCards C1963091 Diarrhea adverse event C0032963 Pregnancy complications, cardiovascular HSDN C0013362 Dysarthrias C0013386 Dyskinesia, drug-induced HSDN C0557874 Global developmental delay C3536827 Glycogenosis with glucoaminophosphaturia MalaCards C0037316 Not enough sleeping C0456511 Paralysis sleep HSDN C0043068 Friderichsen-waterhouse syndrome C0038000 Spleen rupture HSDN C0019572 Hairiness C1857355 Leigh syndrome , french canadian type HPO C0007758 Cerebellar ataxia C1959626 Mevalonic aciduria OrphaNet|HPO|MalaCards C0700292 Arterial hypoxaemia C0032051 Placental insufficiency OrphaNet|MalaCards C0476273 Distress respiratory C1853949 Myasthenia, familial infantile, 1 MalaCards|HPO C0038002 Spleen enlargement C1856245 Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type ii HPO C0027066 Myoclonic jerking C1866282 Ceroid lipofuscinosis, neuronal, 6 MalaCards C0150055 Pain chronic C0003123 Anorexia UMLS C0013404 Respiratory difficulty C3494506 Pseudohypoparathyroidism, type ia HPO C0026821 Cramp C1847759 Muscular dystrophy, congenital, 1c MalaCards|HPO|UMLS C0010038 Corneal opacity disorder C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C1549543 Administration method - pain C0023267 Fibroid tumor HSDN C3641755 Have constipation C4085311 Depression - recess HSDN C4084723 Constipation C1275081 Cardio-facio-cutaneous syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0005683 Urinary bladder calculi (disorder) HSDN C0002965 Crescendo angina C0043251 Wounds and injuries HSDN C0857305 Thrombocytopenia purpura C0023267 Fibroid tumor HSDN C0013421 Dystonia C0004936 Mental disorders HSDN C4085317 Diarrhea frequency C0007873 Uterine cervical neoplasm HSDN C4084768 Usual severity vomiting C0007932 Chagas' disease + no organ inv DiseaseOntology C0028738 Nystagmus C1844776 Cone-rod dystrophy, x-linked, 1 MalaCards|HPO C3274924 Have been coughing C0007137 Squamous cell carcinoma HSDN C2911645 Weight loss adverse event C0062527 Hepatitis b vaccine HSDN C0398650 Idiopathic thrombocytopenia purpura C0017661 Iga glomerulonephritis HSDN C1557397 Adverse event associated with pain C0029396 Heterotopic ossification HSDN C0013604 Edematous C1868703 Bacterial tracheitis HSDN C1961131 Cough adverse event C0220981 Metabolic acidosis HSDN C4084726 Distress cough C0023048 Creeping eruptions HSDN C0026826 High muscle tone C1963134 Hemorrhoids adverse event HSDN C0023380 Lethargy C1318533 Secondary polycythemia OrphaNet|MalaCards C4085211 Pain distress question C0024796 Marfan syndrome HSDN C0027498 Nausea vomiting C2931876 Hirschsprung disease 1 MalaCards C0018991 Paralysis one side of body C0005940 Bone diseases HSDN C0004604 Pain back C2981150 Uranostaphyloschisis HSDN C0518090 Frequency of pain question C0023869 Lithiasis HSDN C0012833 Dizzy C0032343 Poisoning HSDN C0234376 Tremor action C3554519 Cowden syndrome 6 MalaCards C0424755 Fever symptoms C0035242 Respiratory tract diseases HSDN C3887638 Failure to thrive in infant C1838657 Vitamin d hydroxylation-deficient rickets, type 1b HPO C0018808 Murmur C0014544 Epilepsy HSDN C4085549 Dizziness C0029118 Opportunistic infections HSDN C0004134 Dyssynergia C1848922 Hexosaminidase alpha-subunit deficiency (variant b) OrphaNet|MalaCards C3539020 Pelvic pain decreasing in frequency C0037397 Behavior social HSDN C0700072 Encounter due to stillbirth C0265283 Atelosteogenesis, type 1 HPO C0027796 Neuralgias C0151744 Myocardial ischemia HSDN C0030193 Sense of pain C1136321 Hiv-associated lipodystrophy syndrome HSDN C0034933 Abnormal reflexes C0460137 Push down or depress HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006261 Bronchial diseases HSDN C0518090 Frequency of pain question C0028433 Nose neoplasms HSDN C4085661 Usual severity nausea C1299919 Enteric coccidiosis HSDN C0011991 Loose stools C2700553 Omenn syndrome MalaCards|UMLS C1510417 Apraxia of gait C0015423 Eyelid diseases HSDN C0013421 Dystonia C2931092 Maternally inherited leigh syndrome MalaCards C0039870 Leanness C0020557 Hypertriglyceridemia HSDN C0032227 Effusion pleural C0023092 Lassa fever MalaCards C0013604 Edematous C1291329 Transaldolase deficiency OrphaNet|MalaCards C4084773 Bothered by weight gain C0007124 Noninfiltrating intraductal carcinoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0007766 Intracranial aneurysm HSDN C0042024 Urine incontinence C0302148 Blood clot HSDN C2984057 Have nausea C0007117 Basal cell carcinoma HSDN C0037384 Snore C1962963 Osteoporosis adverse event HSDN C0032285 Pneum C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C0016199 Pain flank C2349148 Well differentiated adrenal cortex carcinoma UMLS C0151786 Weakness muscle C0027794 Neural tube defects HSDN C1519353 Skin eruption papular C0281479 Primary systemic amyloidosis MalaCards C0010200 Cough symptom C0003949 Asbestosis HSDN C3146279 Coma C0014544 Epilepsy HSDN C4085317 Diarrhea frequency C0021308 Infarction HSDN C0542476 Forgetful C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C4084776 Weight loss C0001815 Primary myelofibrosis HSDN C0030554 Abnormal sensation C0751549 Neurogenic thoracic outlet syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0010823 Cytomegalovirus infections HSDN C1963064 Anxiety adverse event C2242987 Benign mastocytoma MalaCards C0030554 Abnormal sensation C1384672 Hpt gene HSDN C0848203 Male pelvic pain C0037072 Diseases sigmoid HSDN C0020615 Hypoglycemia nos C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C0020455 Hypergammaglobulinemia C1963138 Hypertension adverse event HSDN C0151786 Weakness muscle C0024121 Lung neoplasms HSDN C0009792 Consciousness disorder C0521542 Brainstem infarct HSDN C0030554 Abnormal sensation C0033923 Psychomotor function HSDN C1557397 Adverse event associated with pain C1136154 Dysfunction, tibialis posterior HSDN C0312416 Morning sickness C0032965 Pregnancy complications, infectious HSDN C1963064 Anxiety adverse event C2936741 Syndrome xxyy OrphaNet|MalaCards C3898969 Have been vomiting C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C1963093 Dizziness adverse event C0022650 Kidney calculi HSDN C0009421 Comatose C0005940 Bone diseases HSDN C4084767 Bothered by vomiting C3714602 Staphylococcal toxic shock syndrome MalaCards C1145670 Failure respiratory C0393814 Hereditary liability to pressure palsies HPO C2984058 Have pain C0011389 Dental plaque HSDN C0020673 Hypothermia (central) (local) C0013922 Embolism HSDN C0026858 Musculoskeletal pain C0011119 Decompression sickness HSDN C0424755 Fever symptoms C0036674 Sensory deprivation HSDN C0007758 Cerebellar ataxia C0268141 Xeroderma pigmentosum, group g HPO C0395923 Multisensory dizziness C0494559 Diseases of inner ear UMLS C0085636 Light sensitivity C0006846 Cutaneous candidiasis HSDN C0184567 Pain acute C0521170 Fracture due to osteoporosis HSDN C0027066 Myoclonic jerking C0032787 Postoperative complications HSDN C0036659 Sensation disorder C0032787 Postoperative complications HSDN C0023014 Developmental disorder language C0004623 Bacterial infections HSDN C0243026 Generalized infection C0400827 Proctitis radiation MalaCards C0008031 Pain chest C0020538 Hypertensive disease HSDN|UMLS C4084768 Usual severity vomiting C0022951 Lactose intolerance HSDN C0010200 Cough symptom C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C2984057 Have nausea C0018801 Heart failure HSDN C0152116 Torticollis spasmodic C1834674 Bethlem myopathy MalaCards|HPO C0036659 Sensation disorder C0022336 Creutzfeldt-jakob disease HSDN C0034933 Abnormal reflexes C1579931 Depressed - symptom HSDN C0004604 Pain back C0002878 Anemia, hemolytic HSDN C4085211 Pain distress question C0085396 Neisseriaceae infections HSDN C0013604 Edematous C0022578 Keratoconus HSDN C3887873 Hearing loss C1855995 L-2-hydroxyglutaric aciduria MalaCards C0013528 Echo speech C0010314 Cri-du-chat syndrome MalaCards C4084724 Usual severity constipation C0020517 Hypersensitivity HSDN C0030193 Sense of pain C0026705 Mucopolysaccharidosis ii HSDN C0013456 Pain ear C0079584 Ichthyosis vulgaris HSDN C0030552 Paralysis partial C0275849 Taboparesis UMLS C0151889 Reflexes tendon increased C0751267 Encephalopathy, subacute necrotizing, infantile MalaCards C0034124 Pupillary disorder C0151699 Intracranial hemorrhages HSDN C4084723 Constipation C0268322 Chester-type porphyria HPO C0018681 Headache, cephalalgia C0011581 Depressive disorder HSDN C4085661 Usual severity nausea C0036983 Septic shock HSDN C0036572 Convulsion C1845450 Cubitus valgus with mental retardation and unusual facies OrphaNet|UMLS|MalaCards C0159055 Swelling, mass and lump of chest C0810299 Other and unspecified lower respiratory disease UMLS C4084773 Bothered by weight gain C0270327 Bedwetting HSDN C0234533 Seizure generalized C2674173 Achondroplasia, severe, with developmental delay and acanthosis nigricans OrphaNet|HPO C0018681 Headache, cephalalgia C0042830 Perception visual HSDN C0018772 Deafness C0795907 Conotruncal anomaly face syndrome OrphaNet C4084773 Bothered by weight gain C0039483 Giant cell arteritis HSDN C0035078 Failure kidney C0027341 Nail-patella syndrome MalaCards|HPO C3496180 Sleep apnea C2930798 Alexanders leukodystrophy MalaCards C0007758 Cerebellar ataxia C0856552 Finger-nose ataxia UMLS C0030200 Intractable pain C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0013390 Cramps menstrual C0034013 Precocious puberty HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2717905 Hereditary angioedema types i and ii HSDN C0018772 Deafness C0018671 Head and neck neoplasms HSDN C1000483 Genus anemia C0032749 Post-kala-azar dermal leishmaniasis MalaCards C3463815 Feel fatigue C1963083 Cholecystitis adverse event HSDN C0000727 Abdomen acute C0039538 Teratoma HSDN C0917816 Deficiency mental C3806403 Continuous spike and waves during slow-wave sleep syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0027127 Myotonia congenita HSDN C0013604 Edematous C0015395 Burn eye HSDN C0575081 Abnormal gait C2931872 Free sialic acid storage disease OrphaNet|MalaCards C1963281 Vomiting adverse event C0600564 Self-efficacy HSDN C4084727 Cough frequency C0007787 Transient ischemic attack HSDN C4085210 Usual severity pain C0036920 Sezary syndrome HSDN C0030193 Sense of pain C3495442 Phantom pain UMLS C1963281 Vomiting adverse event C0002986 Fabry disease MalaCards|HPO C0036572 Convulsion C1860118 Acro fronto facio nasal dysostosis MalaCards C3496180 Sleep apnea C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C0237849 Skin desquamation C3489725 Pseudo-torch syndrome MalaCards C0042571 Vertigo subjective C0343633 Brazilian haemorrhagic fever MalaCards C0349588 Stature short C3151443 Dyskeratosis congenita, autosomal dominant 2 MalaCards C4084774 Have weight loss C0206624 Hepatoblastoma MalaCards C3641756 Have diarrhea C0040127 Thyroid crisis HSDN C0850758 Pain pelvic C0016548 Foreign body migration HSDN C0424755 Fever symptoms C0003467 Anxiety HSDN C1971624 Appetite absent C0004096 Asthma HSDN C0018681 Headache, cephalalgia C0014358 Enterocolitis, pseudomembranous HSDN C0018772 Deafness C2829267 Deafness, autosomal recessive 88 MalaCards C0030193 Sense of pain C0040435 Tooth diseases HSDN C1962972 Proteinuria adverse event C0600518 Choroidal neovascularization HSDN C0018834 Brash C3683846 Chromosome 17p deletion syndrome MalaCards C0020580 Decreased sensation C0010346 Crohn disease HSDN C0024031 Back pain lower back C3495559 Juvenile arthritis HSDN C4084773 Bothered by weight gain C0042875 Vitamin e deficiency HSDN C0022346 Yellow skin C2987191 Pancreatic intraductal papillary mucinous neoplasm, gastric-type UMLS C0007859 Pain neck C0041327 Tuberculosis, pulmonary HSDN C3887873 Hearing loss C0007786 Brain ischemia HSDN C4085642 Level of joint stiffness C0086795 Pfaundler-hurler syndrome HPO C0241210 Speaking delay C1849508 Epilepsy, pyridoxine-dependent MalaCards|HPO C2984057 Have nausea C0013922 Embolism HSDN C3641755 Have constipation C0175713 Aicardi's syndrome MalaCards C2984058 Have pain C0014055 Encephalitis, epidemic HSDN C0015938 Fetal macrosomia C0311468 Increased bilirubin level (finding) HSDN C0004093 Asthenia C0003431 Antisocial personality disorder HSDN C0020672 Body temperature decreased C0003469 Anxiety disorders HSDN C0018834 Brash C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked OrphaNet|HPO C0349588 Stature short C1856797 Estren-dameshek variant of fanconi pancytopenia HPO C0043094 Weight gain C0026946 Mycoses HSDN C0162298 Stiffness joints C0220686 Aase smith syndrome OrphaNet|MalaCards C2032396 Pelvic pain on the right C0206630 Endometrial stromal sarcoma HSDN C2073625 X-ray of chest: pleural effusion C0004943 Behcet syndrome MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0524910 Hepatitis c, chronic MalaCards C0036572 Convulsion C1864871 Chromosome 17q21.31 deletion syndrome OrphaNet|HPO|MalaCards C1963093 Dizziness adverse event C0017181 Gastrointestinal hemorrhage HSDN C0027497 Queasy C0026640 Mouth neoplasms HSDN C0746434 Maxilla pain C0362076 Head problem UMLS C0018681 Headache, cephalalgia C0034494 Rabies (disorder) DiseaseOntology|HSDN|MalaCards C0030193 Sense of pain C0017661 Iga glomerulonephritis HSDN C2237041 Shox gene with short stature C0432252 Osteoporosis with pseudoglioma MalaCards|HPO C0018772 Deafness C0206255 Malaria vaccine HSDN C0018834 Brash C0009374 Colonic disease, functional HSDN C0042798 Vision dim C1840284 Leber congenital amaurosis 11 MalaCards|HPO C0015230 Exanthem C0006849 Oral candidiasis UMLS C2919142 Short stature adverse event C3808988 Fanconi anemia, complementation group q MalaCards C2911645 Weight loss adverse event C0752308 Hypoxia-ischemia, brain HSDN C3887638 Failure to thrive in infant C3810055 Combined oxidative phosphorylation deficiency 19 MalaCards C0085593 Chill C0001175 Acquired immunodeficiency syndrome UMLS C0231807 Dyspnea exertional C1334374 Laryngeal neuroendocrine neoplasm MalaCards C4084773 Bothered by weight gain C2945560 Hemolytic HSDN C4049602 Hyperactivity C0086649 Mps iii c HPO C0018681 Headache, cephalalgia C0338342 Pnet, cerebellar, childhood, recurrent UMLS C0013604 Edematous C0036974 Shock HSDN C4084767 Bothered by vomiting C0036341 Schizophrenia HSDN C4084802 Usual severity diarrhea C0004692 Balantidiasis HSDN C3815497 Cough C0010054 Coronary arteriosclerosis HSDN C2984058 Have pain C0019202 Hepatolenticular degeneration HSDN C0242936 Center pain C0008733 Chylothorax HSDN C0022346 Yellow skin C0002895 Anemia, sickle cell MalaCards|HSDN|HPO|UMLS C3898969 Have been vomiting C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C3541349 Syncope C0042138 Uterine neoplasms HSDN C4084802 Usual severity diarrhea C0003175 Anthrax disease HSDN C0030552 Paralysis partial C1843504 Pontocerebellar hypoplasia type 1 HPO C0344435 Ventricular fibrillation by ecg finding C0268446 Thyrotoxic periodic paralysis MalaCards|HPO C0011168 Disorder deglutition C1837728 Amyotrophic lateral sclerosis 8 (disorder) MalaCards|HPO C2919142 Short stature adverse event C0403553 Renal dysplasia and retinal aplasia (disorder) OrphaNet|HPO C4084766 Vomiting C0027022 Myeloproliferative disease HSDN C0162298 Stiffness joints C3553785 Weill-marchesani syndrome 3 UMLS C0030232 Color loss C0005283 Beta thalassemia OrphaNet|HSDN C0497247 Blood pressure elevation C1306214 Acth-secreting pituitary adenoma HPO C2919142 Short stature adverse event C1842687 Pontocerebellar hypoplasia type 3 (disorder) MalaCards|HPO C0030552 Paralysis partial C3151295 Hypomagnesemia 6, renal MalaCards|HPO C0026826 High muscle tone C0268193 Nadh cytochrome b5 reductase deficiency HPO C2911647 Weight gain adverse event C2698017 Cdisc sdtm marital status terminology HSDN C0013428 Painful urination C0027643 Neoplasm recurrence, local HSDN C4085548 Usual severity dizziness C0021655 Insulin resistance HSDN C0003862 Pain joint C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0241137 Skin pallor C0002875 Cooley's anemia OrphaNet|HPO C0013595 Eczematous dermatitis C1844663 Islets of langerhans, absence of HPO C0575081 Abnormal gait C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C4084773 Bothered by weight gain C0033873 Psychiatry HSDN C0009806 Constipate C0004623 Bacterial infections HSDN C1963090 Dehydration adverse event C0011993 Vipoma OrphaNet|MalaCards C0042940 Disorder of voice C0080040 Polio post syndrome HSDN C4042891 Sleep wake disorders C0006840 Candidiasis HSDN C4084774 Have weight loss C0007137 Squamous cell carcinoma HSDN C4085210 Usual severity pain C0549567 Pigmentation disorders HSDN C0242936 Center pain C2936664 Acquired hypogammaglobulinemia HSDN C0040264 Ear ringing sound C0340629 Aortic aneurysm without mention of rupture nos HSDN C0005745 Blepharoptosis C0238027 Botulism, infantile OrphaNet|MalaCards C0026821 Cramp C0021890 Intraoperative complications HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0032344 Poisoning aspects HSDN C0587047 Mass of trunk C0032266 Emphysema, intestinal UMLS C0005745 Blepharoptosis C1860118 Acro fronto facio nasal dysostosis OrphaNet|MalaCards C1549543 Administration method - pain C1532560 Plasmacytoma - category HSDN C4084776 Weight loss C0006107 Concussion HSDN C0023012 Delay language C0268225 Aspartylglucosaminuria OrphaNet|HPO|MalaCards C0152459 Striae C0268337 Ehlers-danlos syndrome, type 3 (disorder) HPO C0019209 Large liver C1853205 Glycosylphosphatidylinositol deficiency MalaCards|HPO C3641756 Have diarrhea C0270327 Bedwetting HSDN C3463815 Feel fatigue C0003855 Arteriovenous fistula HSDN C0242936 Center pain C3489393 Hiatal hernia HSDN C0557874 Global developmental delay C2675473 Mental retardation, autosomal dominant 5 MalaCards|HPO C0011168 Disorder deglutition C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome MalaCards C0026826 High muscle tone C0752347 Lewy body disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1145628 Autonomic nervous system disorders HSDN C0004310 Auditory disorder process C0005586 Bipolar disorder HSDN C0010200 Cough symptom C0032226 Pleural diseases HSDN C0004134 Dyssynergia C1848813 Thyrocerebral-retinal syndrome MalaCards C1963093 Dizziness adverse event C0205788 Histiocytoid hemangioma HSDN C0587048 Upper extremity mass C0263657 Slap nodules of wrist UMLS C0398650 Idiopathic thrombocytopenia purpura C0003873 Rheumatoid arthritis HSDN C0015469 Facial paralysis C1833373 Inclusion body myopathy, autosomal recessive MalaCards|HPO C0391860 Diffuse inflammations C0544779 Acute diffuse inflammations UMLS C4084774 Have weight loss C0008370 Cholestasis HSDN C0004134 Dyssynergia C2931918 Transketolase defect MalaCards C0206146 Myocardial stunning C0006118 Brain neoplasms HSDN C0036572 Convulsion C0235752 Port-wine stain HSDN|HPO C0277873 Nasal flaring C3150675 Chromosome 15q24 duplication syndrome HPO C3539022 Pelvic pain decreasing in severity C0684743 Malignant neoplasm of muscle HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C0742311 Chest pain site subxiphoid C0741025 Chest problem UMLS C4084775 Usual severity weight loss C0033860 Psoriasis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043325 Xanthomatosis HSDN C2024878 Cardiovascular surgery result: dyspnea C0796274 Brown-vialetto-van laere syndrome HPO C0030193 Sense of pain C3273217 Invasive lobular breast carcinoma, solid variant UMLS C1963252 Tremor adverse event C0034067 Pulmonary emphysema HSDN C0031911 Pigment deposition C1851124 Desmoid disease, hereditary MalaCards C0040264 Ear ringing sound C3810814 Myocardial infarction ecg assessment HSDN C1963077 Bone pain adverse event C0015306 Hereditary multiple exostoses OrphaNet|HPO C0013395 Indigestion C0026848 Myopathy HSDN C0042963 Symptoms vomiting C0162671 Melas syndrome HSDN C3815497 Cough C0032966 Complication, neoplastic pregnancy HSDN C0424755 Fever symptoms C0041948 Uremia HSDN C0036572 Convulsion C0398623 Thrombophilia HSDN C1963184 Nystagmus adverse event C0751273 Infantile globoid cell leukodystrophy MalaCards C0497406 Over weight C0040128 Thyroid diseases HSDN C4084767 Bothered by vomiting C0027643 Neoplasm recurrence, local HSDN C4084802 Usual severity diarrhea C3146297 Study of behavior during childhood HSDN C1963281 Vomiting adverse event C0149931 Migraine disorders MalaCards C3641756 Have diarrhea C0042384 Vasculitis HSDN C0152459 Striae C3553762 Loeys-dietz syndrome 4 MalaCards C1963091 Diarrhea adverse event C0042994 Vulvar diseases HSDN C0086437 Joint hypermobility C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C0015230 Exanthem C0043345 Xeroderma UMLS C0012569 Double vision C0033923 Psychomotor function HSDN C4084764 Shortness of breath C0155883 Chronic obstructive asthma MalaCards C0042024 Urine incontinence C0019829 Hodgkin disease HSDN C0019825 Voice hoarseness C0795864 Smith-magenis syndrome OrphaNet|UMLS|HPO|MalaCards C4084769 Vomiting frequency C0003838 Arterial occlusive diseases HSDN C1963167 Memory impairment adverse event C2960129 Vanishing white matter disease MalaCards C0027066 Myoclonic jerking C0026847 Spinal muscular atrophy HSDN C0266996 Sialectasis C0036093 Salivary gland diseases UMLS C1963184 Nystagmus adverse event C1862099 Brachydactyly-nystagmus-cerebellar ataxia MalaCards C0042798 Vision dim C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C0026838 Spasticity muscle C3151355 Megalencephalic leukoencephalopathy with subcortical cysts 2a MalaCards|HPO|UMLS C0016708 Micturition frequency and polyuria C0028734 Nocturia UMLS C0034155 Thrombotic thrombocytopenic purpura C0007222 Cardiovascular diseases HSDN C2984058 Have pain C0032371 Poliomyelitis HSDN C1962972 Proteinuria adverse event C0376545 Hematologic neoplasms HSDN C4084784 Diarrhea C2937287 Hematolysis HSDN C0232466 Feeding difficulty C2749659 Aicardi-goutieres syndrome 5 (disorder) MalaCards C0349588 Stature short C2931292 Curatolo cilio pessagno syndrome OrphaNet|MalaCards C2126097 Medial right leg soft tissue swelling C0037580 Soft tissue swelling UMLS C4027405 Vulvar redness C0042994 Vulvar diseases UMLS C4042891 Sleep wake disorders C3812141 Linc00914 gene HSDN C0413252 Hypothermia due to exposure C0242231 Coronary stenosis HSDN C0349588 Stature short C4014538 Helsmoortel-van der aa syndrome MalaCards C1959629 Seizure adverse event C1866398 Proteus-like syndrome (disorder) MalaCards C1963281 Vomiting adverse event C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C1962972 Proteinuria adverse event C0752308 Hypoxia-ischemia, brain HSDN C4084726 Distress cough C0023267 Fibroid tumor HSDN C0349588 Stature short C1846949 Brachydactyly, type a1, b MalaCards C0027066 Myoclonic jerking C0022665 Kidney neoplasm HSDN C0851578 Disorder sleep C0022665 Kidney neoplasm HSDN C0233514 Behavior abnormal C2717757 Retinocochleocerebral vasculopathies MalaCards C0011991 Loose stools C0021334 Infectious bovine rhinotracheitis HSDN C4085317 Diarrhea frequency C1546558 Specimen source codes - blister HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043019 Lateral medullary syndrome HSDN C1963170 Hypothermia adverse event C1999266 Depression adverse event HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0006107 Concussion HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0008049 Chicken pox HSDN C0009421 Comatose C0000768 Congenital abnormality HSDN C0011991 Loose stools C0014236 Endophthalmitis HSDN C4084724 Usual severity constipation C0149573 Structure of posterior inferior cerebellar artery HSDN C0018772 Deafness C0265224 Freeman-sheldon syndrome OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C1548578 Location characteristic id - smoking HSDN C0009024 Clonus C1836544 Schindler disease, type i OrphaNet|MalaCards C0017181 Gastrointestinal bleed C0472803 Hypodysfibrinogenemia MalaCards C4085211 Pain distress question C0162790 Harassment sexual HSDN C3641755 Have constipation C1384606 Dyspareunia HSDN C1319543 On examination - right eye diabetic maculopathy C0011164 Abnormal degeneration UMLS C1963087 Constipation adverse event C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0349506 Sun sensitivity C0024138 Lupus erythematosus, discoid MalaCards C0522224 Palsied C0025312 Meningomyelocele HSDN C0009024 Clonus C2677897 Spastic paraplegia 34, x-linked (disorder) MalaCards C0007758 Cerebellar ataxia C0007965 Chediak-higashi syndrome MalaCards|HSDN|HPO C2203646 Jaundice C0010674 Cystic fibrosis HSDN C0030193 Sense of pain C2616767 Mycetoma HSDN C0184567 Pain acute C0037998 Splenic infarction HSDN C3274924 Have been coughing C3161104 Adult plch MalaCards C0026838 Spasticity muscle C0007273 Carotid artery diseases HSDN C0009421 Comatose C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO C0237326 Defecation pain C0268407 Senile cardiac amyloidosis MalaCards C2315100 Pediatric failure to thrive C0795970 Craniofacial digital genital anomalies MalaCards C1963091 Diarrhea adverse event C0018800 Cardiomegaly HSDN C4084766 Vomiting C0220654 Meningeal carcinomatosis HSDN C0269678 Fatigue during pregnancy C0405090 Fatigue during pregnancy - delivered with postnatal comp UMLS C0018681 Headache, cephalalgia C0006114 Cerebral edema HSDN C3887638 Failure to thrive in infant C0004936 Mental disorders HSDN C1279888 Proteinuria of undiagnosed cause C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C1145670 Failure respiratory C0025427 Mercury poisoning OrphaNet|MalaCards C0043094 Weight gain C0031039 Effusion pericardial HSDN C0030193 Sense of pain C0265334 Pachyonychia congenita HSDN C0036572 Convulsion C0023524 Leukoencephalopathy, progressive multifocal HSDN C3829611 Nausea frequency C0023055 Laryngeal neoplasm HSDN C4084776 Weight loss C0020564 Hypertrophy HSDN C0009806 Constipate C0001403 Addison disease OrphaNet C0013604 Edematous C0023176 Lead poisoning HSDN C1963086 Confusion adverse event C0920350 Autoimmune thyroiditis HSDN C1838869 Proximal neurogenic muscle weakness C0221055 Paramyotonia congenita (disorder) MalaCards C0848203 Male pelvic pain C0019693 Hiv infections HSDN C0034124 Pupillary disorder C0037047 Sibling HSDN C3641756 Have diarrhea C0041307 Tuberculosis, bovine HSDN C0086565 Liver function abnormal C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C2024893 Cardiovascular surgery result: fatigue C0011311 Dengue fever HSDN C3539895 Pelvic pain occurs with bowel movement C0037397 Behavior social HSDN C0040822 D tremors C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C2911647 Weight gain adverse event C0702094 Agranulocytosis lab result HSDN C3887638 Failure to thrive in infant C2675463 Chromosome 15q26-qter deletion syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0021361 Female infertility HSDN C2024893 Cardiovascular surgery result: fatigue C0795623 Hepatitis a vaccine, inactivated HSDN C2024893 Cardiovascular surgery result: fatigue C0010346 Crohn disease HSDN C0019079 Bloody sputum C0010054 Coronary arteriosclerosis HSDN|UMLS C0019825 Voice hoarseness C0376527 Neoplasm, skull base HSDN C0018681 Headache, cephalalgia C0022665 Kidney neoplasm HSDN C4084724 Usual severity constipation C0795623 Hepatitis a vaccine, inactivated HSDN C3829611 Nausea frequency C0206062 Lung diseases, interstitial HSDN C0014591 Bleeding nose C0015519 Factor x deficiency MalaCards C3665386 Abnormal vision C3554001 Peroxisome biogenesis disorder 11b MalaCards C1279888 Proteinuria of undiagnosed cause C0017601 Glaucomas HSDN C1963087 Constipation adverse event C0005416 Biliary dyskinesia HSDN C1000483 Genus anemia C0043208 Wolman disease OrphaNet|HPO C0015672 Decreased energy C0001206 Acromegaly OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0017612 Glaucoma, open-angle HSDN C0018784 Deafness sensorineural C3276549 Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy MalaCards C0036572 Convulsion C0036472 Scrub typhus MalaCards C2024878 Cardiovascular surgery result: dyspnea C0263666 Dermatomyositis, childhood type MalaCards C1279888 Proteinuria of undiagnosed cause C0004352 Autistic disorder HSDN C2919142 Short stature adverse event C1859301 Cerebellar hypoplasia with endosteal sclerosis MalaCards C0426579 Anorexia symptom C0042111 Urticaria pigmentosa MalaCards C0039070 Collapse fleeting C0013364 Dysautonomia, familial HSDN C0349588 Stature short C1836437 B-cell immunodeficiency, distal limb anomalies, and urogenital malformations MalaCards C2126061 Right exophthalmos C0015300 Exophthalmos UMLS C0476250 Head neck mass C0267005 Lymphoepithelial mouth cyst UMLS C3887638 Failure to thrive in infant C1857242 Rhizomelic chondrodysplasia punctata, type 2 HPO C1963180 Neck pain adverse event C0001175 Acquired immunodeficiency syndrome HSDN C3641756 Have diarrhea C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C1963086 Confusion adverse event C0019151 Hepatic encephalopathy HSDN C0043094 Weight gain C1553188 Hemolysis - observation HSDN C4084773 Bothered by weight gain C0023448 Lymphoid leukemia HSDN C2237041 Shox gene with short stature C4014954 Neutropenia, severe congenital, 6, autosomal recessive MalaCards C4085862 Bothered by nausea C0041318 Tuberculosis, meningeal HSDN C0015970 Fever unknown origin C0027947 Neutropenia UMLS C0263629 Tumor-like lesions of the skin C0334063 Dyskeratosis follicularis, isolated UMLS C0035078 Failure kidney C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards|HPO C0010038 Corneal opacity disorder C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0277799 Fever intermittent C1304205 Neutrophilic urticaria MalaCards C0857305 Thrombocytopenia purpura C3814530 Skin vesicle HSDN C1963077 Bone pain adverse event C1833372 Hypocalciuric hypercalcemia, familial, type iii MalaCards C4084726 Distress cough C0018024 Goiter, retrosternal HSDN C0973461 Dysphasia C1833473 Dermoid cysts, familial frontonasal MalaCards C1549543 Administration method - pain C0016412 Folic acid deficiency HSDN C0018524 Hallucinate C1112155 Hereditary non-polyposis colorectal cancer syndrome HPO C0349588 Stature short C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards C0034150 Skin purpura C0002884 Hypochromic anemia HSDN C4084784 Diarrhea C0007527 Cecal disease HSDN C0751837 Gait ataxic C0039841 Thiamine deficiency HSDN C4084769 Vomiting frequency C0032226 Pleural diseases HSDN C0012833 Dizzy C1857333 Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia OrphaNet|MalaCards C0151311 Cranial nerve palsy C0023788 Whipple disease MalaCards C2029884 Hearing loss by exam C0023676 Life style HSDN C4084766 Vomiting C2937421 Prostatic hyperplasia HSDN C0241210 Speaking delay C4015141 Mental retardation, autosomal dominant 29 MalaCards C3641756 Have diarrhea C0015300 Exophthalmos HSDN C0030200 Intractable pain C0038454 Cerebrovascular accident HSDN C0027796 Neuralgias C0006663 Calcinosis HSDN C3274924 Have been coughing C0000833 Abscess HSDN C0518090 Frequency of pain question C0036920 Sezary syndrome HSDN C1557397 Adverse event associated with pain C0398623 Thrombophilia HSDN C4085210 Usual severity pain C0014553 Absence epilepsy HSDN C0005745 Blepharoptosis C1969623 Neurofibromatosis, type 1-like syndrome MalaCards|HPO C1963184 Nystagmus adverse event C0751278 Metachromatic leukodystrophy, infant MalaCards C0151786 Weakness muscle C0023055 Laryngeal neoplasm HSDN C0151786 Weakness muscle C0000768 Congenital abnormality HSDN C0019559 Hip arthralgia C1846843 Epiphyseal dysplasia, multiple, 5 MalaCards|HPO|UMLS C1856661 Cornea cloudy C0877024 Schimke immunoosseous dysplasia MalaCards|HPO C0020505 Excessive eating C1846171 Lissencephaly, x-linked, 2 MalaCards C2242996 Tingling C0238386 Cronkhite-canada disease MalaCards C0018808 Murmur C0152417 Congenital stenosis aortic valve MalaCards C0009421 Comatose C1550639 Specimen type - fistula HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C2051831 Pectus excavatum HSDN C0001707 Aerophagia C0009492 Compartment syndromes HSDN C0003862 Pain joint C0264939 Systemic vasculitis HSDN C0034150 Skin purpura C0853697 Neutrophil count decreased HSDN C0011168 Disorder deglutition C3275460 Mental retardation, x-linked, syndromic 17 MalaCards C0030193 Sense of pain C1334708 Metaplastic breast carcinoma UMLS C4085211 Pain distress question C0242188 Spider bites HSDN C1971624 Appetite absent C2930674 Babesioses, human MalaCards C1549543 Administration method - pain C0036601 Self mutilation HSDN C0848203 Male pelvic pain C0242350 Erectile dysfunction HSDN C0497247 Blood pressure elevation C1858592 Carney triad MalaCards C1963091 Diarrhea adverse event C0242216 Biliary calculi HSDN C0033377 Caudal displacement C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C0009421 Comatose C0020598 Hypocalcemia HSDN C0575081 Abnormal gait C3695063 Charcot-marie-tooth disease, type 4b3 MalaCards C1557397 Adverse event associated with pain C0019156 Hepatic veno-occlusive disease HSDN C0042571 Vertigo subjective C1956346 Coronary artery disease HSDN C0232466 Feeding difficulty C1846790 Joubert syndrome 4 (disorder) MalaCards C4084767 Bothered by vomiting C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0086437 Joint hypermobility C3150675 Chromosome 15q24 duplication syndrome HPO C0750937 Appendicular ataxia C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C4085210 Usual severity pain C1000587 Pemphigus HSDN C0005745 Blepharoptosis C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards|HPO C2984058 Have pain C0740392 Infarction, middle cerebral artery HSDN C3463815 Feel fatigue C0019112 Hemorrhoids HSDN C4084788 Have dizziness C0270639 Lateral sinus thrombosis HSDN C3541349 Syncope C0018188 Granuloma HSDN C4084723 Constipation C0517555 Venous thrombosis after immobility HSDN C0040485 Wryneck C0005967 Bone neoplasms HSDN C2984058 Have pain C0040336 Tobacco use disorder HSDN C0033774 Skin pruritus C1332254 Ampulla of vater undifferentiated carcinoma UMLS C0018681 Headache, cephalalgia C1266180 Large cell medulloblastoma UMLS C4084802 Usual severity diarrhea C0007134 Renal cell carcinoma HSDN C4084773 Bothered by weight gain C0018051 Gonadal dysgenesis HSDN C1961131 Cough adverse event C1848814 Thymoma, familial MalaCards C0007758 Cerebellar ataxia C1839566 Charcot-marie-tooth disease, x-linked recessive, 5 MalaCards|HPO C0018777 Deafness, conductive C0029396 Heterotopic ossification HSDN C0518090 Frequency of pain question C0031046 Pericarditis HSDN C0476212 Dysfunctions associated with arousal from sleep C0154565 Non-organic sleep disorder UMLS C0013362 Dysarthrias C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO C0018772 Deafness C0015934 Fetal growth retardation HSDN C4085317 Diarrhea frequency C1264008 Chronic cold agglutinin disease MalaCards C0231712 Gait waddling C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C4085549 Dizziness C0009395 Color perception HSDN C0015402 Hemorrhage eye C0015456 Facial dermatoses HSDN C0454542 Acquired stuttering C0454533 Disorder of fluency UMLS C1962972 Proteinuria adverse event C0027819 Neuroblastoma HSDN C0349588 Stature short C0265339 Borjeson-forssman-lehmann syndrome MalaCards|HPO C2029884 Hearing loss by exam C0003467 Anxiety HSDN C0037315 Breathing disorder during sleeping C3279843 Mosaic variegated aneuploidy syndrome 2 MalaCards C4084802 Usual severity diarrhea C0242422 Parkinsonian disorders HSDN C4084802 Usual severity diarrhea C0268543 Hyperammonemia, type iii MalaCards C0518090 Frequency of pain question C0001197 Acrodermatitis HSDN C1279888 Proteinuria of undiagnosed cause C0334299 Carcinoid tumor no icd-o subtype HSDN C4084784 Diarrhea C0042131 Uterine diseases HSDN C3827868 Tachycardia by ecg finding C0272118 Warm autoimmune hemolytic anemia MalaCards C0018772 Deafness C0035078 Kidney failure HSDN C3463815 Feel fatigue C0022650 Kidney calculi HSDN C0812426 Kidney problem C0748288 Renal decompensation UMLS C4084725 Usual severity cough C1253943 Fluid in the chest HSDN C4084773 Bothered by weight gain C0002726 Amyloidosis HSDN C0030554 Abnormal sensation C0393814 Hereditary liability to pressure palsies OrphaNet|HPO C0029163 Hemorrhage mouth C0036601 Self mutilation HSDN C0020673 Hypothermia (central) (local) C0002940 Aneurysm HSDN C0018991 Paralysis one side of body C0030353 Papilledema HSDN C0009792 Consciousness disorder C0001175 Acquired immunodeficiency syndrome HSDN C0020673 Hypothermia (central) (local) C0010308 Congenital hypothyroidism OrphaNet|MalaCards C0026821 Cramp C0007785 Cerebral infarction HSDN C1279888 Proteinuria of undiagnosed cause C0030354 Papilloma HSDN C0043094 Weight gain C1552262 Nurse practitioner - family HSDN C0013404 Respiratory difficulty C0006145 Breast diseases HSDN C0018772 Deafness C2930815 Acute cerebral gaucher disease MalaCards C0033774 Skin pruritus C0861861 Squamous cell bile duct carcinoma UMLS C0039870 Leanness C0919267 Ovarian neoplasm HSDN C0030554 Abnormal sensation C0040136 Thyroid neoplasm HSDN C0020305 Fetal edema C0008626 Congenital chromosomal disease HSDN C0024032 Birth weight subnormal C0796117 Pitt syndrome MalaCards C0151740 Intracranial hypertension C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0241210 Speaking delay C1858054 Bardet-biedl syndrome 6 HPO C0036572 Convulsion C0751053 Confusion postictal UMLS C0424755 Fever symptoms C0037999 Splenic neoplasms HSDN C0024031 Back pain lower back C0001584 Adolescent psychology HSDN C4084724 Usual severity constipation C3683846 Chromosome 17p deletion syndrome MalaCards C0038002 Spleen enlargement C2749759 Macrothrombocytopenia-stomatocytosis, mediterranean HPO C3463815 Feel fatigue C0032749 Post-kala-azar dermal leishmaniasis MalaCards C0851578 Disorder sleep C0021364 Male infertility HSDN C3539893 Pelvic pain occurs with intercourse C0042253 Vaginal fistula HSDN C0033774 Skin pruritus C1842036 Giant pigmented hairy nevus MalaCards|HPO C2029884 Hearing loss by exam C0040411 Tongue neoplasms HSDN C0022346 Yellow skin C0242723 Parasitemia HSDN C0085631 Abnormal excitement C0037274 Dermatologic disorders HSDN C1963086 Confusion adverse event C2239176 Liver carcinoma HSDN C0424755 Fever symptoms C0035920 Rubella DiseaseOntology|HSDN|MalaCards C3274924 Have been coughing C0751552 Malignant neoplasm of thymus MalaCards C0085593 Chill C0012624 Diskitis HSDN C0030554 Abnormal sensation C0016053 Fibromyalgia HSDN C0518090 Frequency of pain question C0036974 Shock HSDN C4085210 Usual severity pain C0041755 Adverse reaction to drug HSDN C2984058 Have pain C4085635 Appetite quality question HSDN C4085317 Diarrhea frequency C1704436 Peripheral arterial diseases HSDN C0018772 Deafness C3152102 Ush1d/f, cdh23/pcdh15, digenic HPO C0518090 Frequency of pain question C0042341 Varicocele HSDN C0494475 Seizure generalized tonic clonic C1832386 Diabetes mellitus, transient neonatal, 1 MalaCards|HPO C0085636 Light sensitivity C1848410 Xeroderma pigmentosum, variant type OrphaNet|HPO|MalaCards C1145670 Failure respiratory C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C1963065 Apnea adverse event C1855606 Burton syndrome MalaCards C2237041 Shox gene with short stature C1328931 Multiple lentigines MalaCards C0039870 Leanness C0206255 Malaria vaccine HSDN C0242936 Center pain C0020651 Hypotension, orthostatic HSDN C2203646 Jaundice C0009241 Cognition disorders HSDN C1963087 Constipation adverse event C4084909 Depression subordinate domain HSDN C0000737 Abdomen pain C1851347 Familial mediterranean fever, autosomal dominant HPO|UMLS C4085317 Diarrhea frequency C0009326 Collagen diseases HSDN C1260880 Nasal drip C1334647 Maxillary sinus squamous cell carcinoma UMLS C4085549 Dizziness C0043251 Wounds and injuries HSDN C1279888 Proteinuria of undiagnosed cause C0079487 Helicobacter infections HSDN C1549543 Administration method - pain C0013312 Dupuytren contracture HSDN C0009460 Communication impairment C0030567 Parkinson disease HSDN C0002962 Angina C0080274 Urinary retention HSDN C0027497 Queasy C0205770 Choroid plexus papilloma HPO|UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0751908 Vestibular neuronitis HSDN C0018681 Headache, cephalalgia C3665377 Keratinizing epidermoid carcinoma of nasopharynx UMLS C0020580 Decreased sensation C0752181 Central nervous system parasitic infections HSDN C1963091 Diarrhea adverse event C3163620 Hypotension adverse event HSDN C4085222 Nausea C0013080 Down syndrome HSDN C4085211 Pain distress question C0005683 Urinary bladder calculi (disorder) HSDN C0013604 Edematous C1262481 Eosinophilic gastroenteritis MalaCards C0040034 Thrombocytopenia C0376300 Dengue shock syndrome MalaCards C4085862 Bothered by nausea C0003864 Arthritis HSDN C4085661 Usual severity nausea C0268647 Lysinuric protein intolerance MalaCards|HPO C0242936 Center pain C0032797 Postpartum hemorrhage HSDN C0042571 Vertigo subjective C0151699 Intracranial hemorrhages HSDN C3539889 Pelvic pain increasing in severity C0041952 Uerterolithiasis HSDN C0030200 Intractable pain C0041296 Tuberculosis HSDN C0000737 Abdomen pain C2749485 Nblst1 HPO C0018991 Paralysis one side of body C0023530 Leukopenia HSDN C2024893 Cardiovascular surgery result: fatigue C0281479 Primary systemic amyloidosis MalaCards C2984058 Have pain C0206239 Cubital syndrome tunnel HSDN C0007758 Cerebellar ataxia C0751781 Dentatorubral-pallidoluysian atrophy HPO|UMLS C1963093 Dizziness adverse event C0003469 Anxiety disorders HSDN C0221752 Rbc urine C0268382 Amyloid nephropathy MalaCards C4085210 Usual severity pain C0010635 Cystadenoma, mucinous HSDN C4084776 Weight loss C0409988 Focal nodular myositis MalaCards C0037199 Sinus infection C1844376 Granulomatous disease, chronic, x-linked MalaCards C4084727 Cough frequency C1866983 Scleroderma, familial progressive MalaCards C2911645 Weight loss adverse event C0017661 Iga glomerulonephritis HSDN C0020580 Decreased sensation C0007222 Cardiovascular diseases HSDN C0019559 Hip arthralgia C0023518 Leukocytosis UMLS C0013405 Dyspnea, paroxysmal C0009730 Spinal meningocele HSDN C1768507 Yellow nails C0221348 Hereditary lymphedema and yellow nails OrphaNet|UMLS|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0236969 Substance-related disorders HSDN C0022638 Ketosis C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C0857305 Thrombocytopenia purpura C0023448 Lymphoid leukemia HSDN C1313921 Urinomas C0042140 Uterine prolapse HSDN C1963167 Memory impairment adverse event C0022336 Creutzfeldt-jakob disease MalaCards|HPO C4084724 Usual severity constipation C0525042 Feeding and eating disorders of childhood HSDN C4084769 Vomiting frequency C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C0024031 Back pain lower back C0013295 Duodenal ulcer HSDN C0086437 Joint hypermobility C2674127 Loeys dietz syndrome, type 2a (disorder) MalaCards C0085602 Polydypsia C1846979 Senior-loken syndrome 4 MalaCards|HPO|UMLS C4085317 Diarrhea frequency C2062326 Eosinophilic enteropathy OrphaNet|MalaCards C0020673 Hypothermia (central) (local) C0023467 Leukemia, myelocytic, acute HSDN C3898969 Have been vomiting C0000814 Abortion, missed HSDN C4084775 Usual severity weight loss C0085437 Meningitis, bacterial HSDN C4084724 Usual severity constipation C1864996 Enteric neuropathy, familial MalaCards C0003467 Angst C2932716 Pseudohypoparathyroidism type 1c HPO C0004093 Asthenia C0014548 Epilepsy, generalized HSDN C1557397 Adverse event associated with pain C0242659 Female homosexual HSDN C4085661 Usual severity nausea C0003078 Aniseikonia HSDN C1963281 Vomiting adverse event C0342474 Lipoid congenital adrenal hyperplasia OrphaNet C0011206 Delirium acute C0030568 Parkinsonism, postencephalitic HSDN C1961131 Cough adverse event C3541306 Plasmodium measurement HSDN C0085631 Abnormal excitement C0040479 Torsades de pointes HSDN C3641756 Have diarrhea C0042018 Urinary calculi HSDN C0018926 Emesis bloody C0238339 Hereditary pancreatitis HSDN C0009806 Constipate C2937421 Prostatic hyperplasia HSDN C0234376 Tremor action C4225383 Lichtenstein-knorr syndrome UMLS C1963091 Diarrhea adverse event C1261470 Congenital meningocele HSDN C2024893 Cardiovascular surgery result: fatigue C0039614 Tetanus HSDN C0018681 Headache, cephalalgia C0205788 Histiocytoid hemangioma HSDN C0036659 Sensation disorder C0040456 Tooth impaction HSDN C0033774 Skin pruritus C0027962 Melanocytic nevus HSDN C4084725 Usual severity cough C0149931 Migraine disorders HSDN C0005779 Clotting C1838120 Hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities OrphaNet|MalaCards C1962972 Proteinuria adverse event C1456865 Ureteral calculi HSDN C4084767 Bothered by vomiting C1855369 Maple syrup urine disease, type ia HPO C4084773 Bothered by weight gain C0037997 Splenic diseases HSDN C0004134 Dyssynergia C0268251 Gaucher disease, type 3 (disorder) OrphaNet|UMLS|HPO|MalaCards C0017672 Pain tongue C1000483 Genus anemia HSDN C1069915 Vertigo C0018939 Hematological disease HSDN C1963184 Nystagmus adverse event C1837873 Leber congenital amaurosis 9 (disorder) MalaCards|HPO C0000727 Abdomen acute C0162651 Gastric outlet obstruction HSDN C1963281 Vomiting adverse event C1546949 Event consequence - death HSDN C0015970 Fever unknown origin C0007873 Uterine cervical neoplasm HSDN C3463815 Feel fatigue C0021670 Insulinoma MalaCards|HPO C3898969 Have been vomiting C0024841 Matrimony, matrimonial HSDN C0036572 Convulsion C4225333 Hypomagnesemia, seizures, and mental retardation UMLS C0018524 Hallucinate C0543918 Schizophrenia 10 MalaCards C0004134 Dyssynergia C4084841 Joubert syndrome 24 UMLS C0028738 Nystagmus C1274795 Urban schosser spohn syndrome OrphaNet|MalaCards C0151786 Weakness muscle C0035410 Rhabdomyolysis MalaCards C0332573 Macula C0264743 Rheumatic fever without heart involvement MalaCards C0030486 Extremity paralysis, lower C0009450 Disease caused by microorganism HSDN C0015672 Decreased energy C0009782 Connective tissue diseases HSDN C2029884 Hearing loss by exam C0004030 Aspergillosis HSDN C0041657 Consciousness loss C0347766 Skull fracture depressed HSDN C0151786 Weakness muscle C3469605 Pseudohypoaldosteronism, type iid MalaCards C0033377 Caudal displacement C0023264 Leigh disease MalaCards|HPO C0010520 Skin cyanosis C3151421 Cyanosis, transient neonatal MalaCards|HPO|UMLS C0009806 Constipate C0243026 Sepsis HSDN C0018991 Paralysis one side of body C0027708 Nephroblastoma HSDN C1963137 Hydrocephalus adverse event C2931888 Pfeiffer type acrocephalosyndactyly MalaCards C3463815 Feel fatigue C0038441 Stress disorders, traumatic HSDN C3539891 Pelvic pain to the rear C0017416 Genital neoplasms, female HSDN C0009421 Comatose C0030305 Pancreatitis HSDN C0024032 Birth weight subnormal C2674937 Chromosome 10q26 deletion syndrome MalaCards C0242936 Center pain C0006309 Brucellosis HSDN C0011570 Monopolar depression C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C1963170 Hypothermia adverse event C0012691 Dislocations HSDN C2919142 Short stature adverse event C1862178 Cole carpenter syndrome OrphaNet|HPO|MalaCards C2203646 Jaundice C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C3815497 Cough C0085232 Diverticulum zenker HSDN C1963087 Constipation adverse event C3160718 Parkinson disease, late-onset MalaCards|HPO C0150055 Pain chronic C1269683 Major depressive disorder HSDN C3532678 Dizziness due to drug C0277579 Drug-related disorders UMLS C1963091 Diarrhea adverse event C0036982 Shock, hemorrhagic HSDN C0151908 Dry skin C0079588 Ichthyosis, x-linked OrphaNet|HPO|MalaCards C4084784 Diarrhea C0035439 Rheumatic heart disease HSDN C0032617 High urine output C1963059 Adrenal insufficiency adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0034063 Pulmonary edema HSDN C0042798 Vision dim C0012752 Distance discrimination HSDN C1961131 Cough adverse event C2586211 Thrombosis of blood vessel HSDN C2700617 Irritation - emotion C0751434 Classical phenylketonuria MalaCards|HPO C2919142 Short stature adverse event C0036391 Schwartz-jampel syndrome OrphaNet|HPO|MalaCards C0034150 Skin purpura C0005695 Bladder neoplasm HSDN C2984057 Have nausea C0019557 Hip fx HSDN C0424810 Periorbital swelling C0362076 Head problem UMLS C4084774 Have weight loss C0314657 Genetic predisposition HSDN C0020580 Decreased sensation C0027651 Tumor HSDN C1549543 Administration method - pain C0025958 Microcephaly HSDN C4085862 Bothered by nausea C0023860 Listeriosis DiseaseOntology|MalaCards C1963086 Confusion adverse event C3542413 Cdisc adas-cog - comprehension HSDN C4042891 Sleep wake disorders C0030297 Pancreatic neoplasm HSDN C2237041 Shox gene with short stature C0024454 Maffucci syndrome OrphaNet|HPO|MalaCards C3541349 Syncope C0025202 Melanoma HSDN C0026821 Cramp C0020701 Somatization disorder HSDN C0027066 Myoclonic jerking C0005604 Trauma birth HSDN C4084802 Usual severity diarrhea C0795956 Chylomicron retention disease MalaCards|HPO C4084774 Have weight loss C0007787 Transient ischemic attack HSDN C1961131 Cough adverse event C0151636 Premature ventricular contractions HSDN C0003862 Pain joint C0343068 Familial cold urticaria MalaCards|HPO C0018681 Headache, cephalalgia C0026896 Myasthenia gravis HSDN C0015402 Hemorrhage eye C0015523 Factor xi deficiency HSDN C4084725 Usual severity cough C3244301 Coverage level - family HSDN C0557874 Global developmental delay C2752001 Growth retardation, developmental delay, coarse facies, and early death HPO C0424755 Fever symptoms C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C1963281 Vomiting adverse event C0011881 Diabetic nephropathy HSDN C0013378 Dysgensia C0040100 Thymoma HSDN C3887638 Failure to thrive in infant C0037769 West syndrome HSDN C0151825 Ostalgia C0264080 Juvenile osteoporosis OrphaNet|HPO C1557397 Adverse event associated with pain C0015652 Fascioliasis HSDN C0178417 Anhedonia C0812393 Cancer patients and suicide and depression HSDN C1549543 Administration method - pain C0556482 Protection sex HSDN C0018777 Deafness, conductive C0265308 Baller-gerold syndrome MalaCards|HPO C3898969 Have been vomiting C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4042891 Sleep wake disorders C0038525 Subarachnoid hemorrhage HSDN C0282005 Scrotum swelling C0262404 Cerebellar degeneration UMLS C0030486 Extremity paralysis, lower C0007133 Carcinoma, papillary HSDN C4084768 Usual severity vomiting C0022107 Irritable mood HSDN C4084766 Vomiting C0017601 Glaucomas HSDN C0221752 Rbc urine C0263591 Lupus erythematosus drug induced MalaCards C2096293 Ent surgical result ear vertigo C1535917 Nipah virus infection MalaCards C0015672 Decreased energy C0034063 Pulmonary edema HSDN C0242936 Center pain C3889576 Euphoria HSDN C0002962 Angina C2242765 Acquired spondylolisthesis HSDN C2919142 Short stature adverse event C0751918 Cockayne pelizaeus merzbacher disease MalaCards C2984058 Have pain C0038166 Staphylococcal skin infections HSDN C1000483 Genus anemia C1850126 Osteopetrosis, mild autosomal recessive form MalaCards|HPO C0031911 Pigment deposition C3888004 Hermansky-pudlak syndrome 5 MalaCards C0424755 Fever symptoms C0031347 Pharyngeal neoplasms HSDN C1069915 Vertigo C0206255 Malaria vaccine HSDN C0020458 Hyperhydrosis C0545044 Acrokeratoelastoidosis of costa OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0001418 Adenocarcinoma HSDN C1384666 Decreased hearing C0037369 Smoking HSDN C0454644 Delayed language development C0268631 Succinic semialdehyde dehydrogenase deficiency MalaCards|HPO C0030193 Sense of pain C0280331 Supraglottic verrucous carcinoma UMLS C1000483 Genus anemia C0268250 Gaucher disease, type 2 (disorder) MalaCards|HPO C0020673 Hypothermia (central) (local) C0338503 Septo-optic dysplasia HSDN C0522224 Palsied C0025297 Viral meningitis HSDN C0024312 Lymphocytopenia C3810147 Immunodeficiency 19 MalaCards C0018784 Deafness sensorineural C3808953 Nephrotic syndrome, type 8 MalaCards C1962972 Proteinuria adverse event C0018944 Hematoma HSDN C0917816 Deficiency mental C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C0042940 Disorder of voice C0021890 Intraoperative complications HSDN C4084802 Usual severity diarrhea C0013533 Echovirus infections HSDN C0041834 Erythematous condition C2930812 Generalized elastolysis MalaCards C0042798 Vision dim C0087012 Ataxia, spinocerebellar HSDN C0020903 Illusion C0233828 Intuition HSDN C0151786 Weakness muscle C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C4085222 Nausea C0012691 Dislocations HSDN C4084775 Usual severity weight loss C0009241 Cognition disorders HSDN C0270948 Neurogenic muscular atrophy C2931842 Diaphyseal dysplasia 1, progressive MalaCards|HPO C0036572 Convulsion C1857252 2,4-dienoyl-coa reductase deficiency MalaCards|UMLS C1549543 Administration method - pain C0032578 Polyploidy HSDN C0349588 Stature short C3808184 Mental retardation, autosomal dominant 22 MalaCards C2984058 Have pain C0027831 Neurofibromatosis 1 HSDN C0015672 Decreased energy C0001973 Alcoholic intoxication, chronic HSDN C0037763 Spasm C0043145 Whiplash HSDN C0036572 Convulsion C0002994 Angioedema HSDN C0030193 Sense of pain C0035436 Rheumatic fever HSDN C3539896 Pelvic pain occurs with urination C0001418 Adenocarcinoma HSDN C0151818 Opisthotonos C0085292 Stiff-person syndrome MalaCards|UMLS C0015970 Fever unknown origin C0037313 Sleep HSDN C0018681 Headache, cephalalgia C0752287 Sleep disorders, intrinsic HSDN C0040034 Thrombocytopenia C0026205 Miosis disorder MalaCards C3541349 Syncope C0020544 Renal hypertension HSDN C0000737 Abdomen pain C0268307 Conjugated hyperbilirubinemia MalaCards C2203646 Jaundice C0032087 Plant poisoning HSDN C4084767 Bothered by vomiting C0014869 Peptic esophagitis HSDN C4084802 Usual severity diarrhea C1843116 Bile acid synthesis defect, congenital, 1 MalaCards|HPO C0011991 Loose stools C0020649 Hypotension HSDN C0016382 Cutaneous vascular engorgement C2717899 Upper extremity deep vein thrombosis HSDN C0085128 Cardiac output elevated C0002886 Anemia, macrocytic HSDN C0518090 Frequency of pain question C0024131 Lupus vulgaris HSDN C0004941 Behavioral symptoms C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C1963087 Constipation adverse event C0085278 Antiphospholipid syndrome HSDN C2700617 Irritation - emotion C1384514 Conn syndrome MalaCards C2911645 Weight loss adverse event C1866552 Paragangliomas 2 (disorder) MalaCards C2203646 Jaundice C0033923 Psychomotor function HSDN C0015469 Facial paralysis C1837122 Myasthenic syndrome, congenital, fast-channel MalaCards|HPO C3887873 Hearing loss C0038436 Post-traumatic stress disorder HSDN C4084775 Usual severity weight loss C0020517 Hypersensitivity HSDN C0022346 Yellow skin C2983423 Stage iii hepatocellular carcinoma UMLS C0036572 Convulsion C2678415 Hyperphenylalaninemia, bh4-deficient, due to partial pts deficiency HPO C3539890 Pelvic pain causes awakening at night C0432264 Axial osteosclerosis MalaCards C0751495 Seizure focal C3494976 Migrating partial seizures in infancy UMLS C3887638 Failure to thrive in infant C1956093 Paris-trousseau thrombocytopenia MalaCards C3887873 Hearing loss C0032343 Poisoning HSDN C2024893 Cardiovascular surgery result: fatigue C0162526 Aids-related opportunistic infections HSDN C1962972 Proteinuria adverse event C0020479 Hyperlipoproteinemia type iii HSDN C3815497 Cough C0006272 Bronchiolitis obliterans HSDN C0013604 Edematous C0032326 Pneumothorax HSDN C0151786 Weakness muscle C3469606 Pseudohypoaldosteronism, type iie MalaCards C3274924 Have been coughing C0016548 Foreign body migration HSDN C4085317 Diarrhea frequency C0028758 Bonding HSDN C0015732 Feces incontinence C1997362 Non-neurogenic neurogenic bladder MalaCards C0494475 Seizure generalized tonic clonic C1858493 Febrile convulsions, familial, 4 HPO C0239377 Upper extremity pain C0750929 Arnold-chiari malformation, type i MalaCards|UMLS C3898969 Have been vomiting C2981150 Uranostaphyloschisis HSDN C0270948 Neurogenic muscular atrophy C0795910 Cowchock syndrome OrphaNet|HPO|MalaCards C0015970 Fever unknown origin C0016658 Fracture bone HSDN C2919142 Short stature adverse event C2745959 Spondyloepiphyseal dysplasia, congenita OrphaNet|HPO C3641756 Have diarrhea C0018213 Graves disease HSDN C0015402 Hemorrhage eye C0273483 Cranial nerve injury HSDN C1549543 Administration method - pain C0027022 Myeloproliferative disease HSDN C0024312 Lymphocytopenia C0004135 Ataxia telangiectasia OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0919267 Ovarian neoplasm HSDN C1963063 Anorexia adverse event C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C0030193 Sense of pain C1336699 Telangiectatic glomangioma UMLS C0012569 Double vision C1704272 Benign prostatic hyperplasia HSDN C0030193 Sense of pain C3840252 Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma UMLS C0332563 Papulae C1968804 Plasminogen deficiency, type i MalaCards C0085632 Listlessness C1868594 Perry syndrome OrphaNet|UMLS|HPO|MalaCards C0231791 In toe C0175691 Dubowitz syndrome MalaCards|HPO C0577560 Eye mass C0033999 Pterygium UMLS C1145670 Failure respiratory C1862939 Amyotrophic lateral sclerosis 1 MalaCards C0232503 Bleeding umbilical C1290864 Abdominal disorders UMLS C0812426 Kidney problem C0022660 Kidney failure, acute UMLS C0497406 Over weight C1556682 Adverse event associated with infection HSDN C0030193 Sense of pain C0020476 Hyperlipoproteinemias HSDN C3203358 Alveolar hypoventilation C0153064 Encephalomyelitis, western equine HSDN C0022346 Yellow skin C0221757 Alpha 1-antitrypsin deficiency OrphaNet|HPO C1963091 Diarrhea adverse event C0003496 Aortic rupture HSDN C0240735 Personality change C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C1971624 Appetite absent C2609414 Acute kidney injury HSDN C0518090 Frequency of pain question C0021099 Impetigo HSDN C0028738 Nystagmus C1135161 Stage 4s neuroblastoma MalaCards C0237326 Defecation pain C0265498 48, xxxy syndrome OrphaNet|MalaCards C0000737 Abdomen pain C0030446 Paralytic ileus UMLS C0033377 Caudal displacement C0795949 Galloway mowat syndrome HPO C0027796 Neuralgias C0034735 Raynaud phenomenon HSDN C0497247 Blood pressure elevation C0403557 Glomerulopathy with giant fibrillar deposits MalaCards C4042891 Sleep wake disorders C0033873 Psychiatry HSDN C1963091 Diarrhea adverse event C0010606 Adenoid cystic carcinoma HSDN C0022107 Fussiness C0038868 Progressive supranuclear palsy HPO C0020438 Hypercalciuria C1864729 Hyperparathyroidism 3 MalaCards C2984058 Have pain C0031212 Personality disorders HSDN C0264611 Apraxia of speech C2363129 Benign rolandic epilepsy MalaCards C4084773 Bothered by weight gain C0518450 Spinal fractures HSDN C0012833 Dizzy C0029888 Otitis media purulent HSDN C1519353 Skin eruption papular C0349658 Trichoepithelioma MalaCards C0030193 Sense of pain C0003431 Antisocial personality disorder HSDN C0349588 Stature short C3502054 Dentoleukoencephalopathy MalaCards C0030193 Sense of pain C0005891 Bodies image HSDN C0036572 Convulsion C2750798 Polymicrogyria with optic nerve hypoplasia HPO|UMLS C4084897 Sleep disturbance subordinate domain C1848201 Subcortical band heterotopia MalaCards C0022346 Yellow skin C1335257 Pretext stage 3 hepatoblastoma UMLS C0349588 Stature short C3159322 Spondyloepiphyseal dysplasia, maroteaux type OrphaNet|MalaCards C0085631 Abnormal excitement C0011071 Sudden death HSDN C0007758 Cerebellar ataxia C0027947 Neutropenia HSDN C4084802 Usual severity diarrhea C0001314 Acute disease HSDN C0850758 Pain pelvic C0023895 Liver diseases HSDN C3641755 Have constipation C0012979 Canine disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029434 Osteogenesis imperfecta HSDN C4084802 Usual severity diarrhea C0008370 Cholestasis HSDN C0007758 Cerebellar ataxia C0026272 Mixed connective tissue disease HSDN C0349588 Stature short C1851536 Epiphyseal dysplasia, multiple, with myopia and conductive deafness HPO C0011206 Delirium acute C0004623 Bacterial infections HSDN C0700078 Deep tendon reflex decrease C3150416 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 MalaCards|HPO C1549543 Administration method - pain C2984330 Chagas disease pathway HSDN C0020538 Hbp C0013581 Ectopia lentis MalaCards|HPO C0020673 Hypothermia (central) (local) C0016483 Food preferences HSDN C1549543 Administration method - pain C0016436 Folliculitis HSDN C0518090 Frequency of pain question C0004144 Atelectasis HSDN C1963180 Neck pain adverse event C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0085636 Light sensitivity C0265336 Senter syndrome OrphaNet|UMLS|HPO|MalaCards C1963281 Vomiting adverse event C0037274 Dermatologic disorders HSDN C0027498 Nausea vomiting C0011854 Diabetes mellitus, insulin-dependent UMLS C0577572 Mass of musculoskeletal structure C0409780 Villonodular synovitis, hand UMLS C0013428 Painful urination C0042075 Urologic diseases HSDN|UMLS C1963063 Anorexia adverse event C2706915 Language:-:point in time:^patient:- HSDN C0040034 Thrombocytopenia C1845837 Dyserythropoietic anemia with thrombocytopenia MalaCards C1963184 Nystagmus adverse event C0033835 Pseudopseudohypoparathyroidism MalaCards|HPO C0026821 Cramp C0206716 Ganglioglioma HSDN C0003811 Cardiac rhythm disturbance C1956258 Familial thrombotic thrombocytopenic purpura MalaCards C0027497 Queasy C0014121 Bacterial endocarditis HSDN C1963086 Confusion adverse event C1457883 Aggressive reaction HSDN C4085661 Usual severity nausea C3495422 Finding relating to sexuality and sexual activity HSDN C0030552 Paralysis partial C0034885 Rectal neoplasms HSDN C2984058 Have pain C0018567 Hand dermatoses HSDN C0015672 Decreased energy C2930674 Babesioses, human MalaCards C3541349 Syncope C2015933 Outcomes otolaryngology hearing HSDN C4084773 Bothered by weight gain C0007138 Carcinoma, transitional cell HSDN C0349588 Stature short C3554002 Pbd12a MalaCards C3539889 Pelvic pain increasing in severity C0021831 Intestinal diseases HSDN C4084766 Vomiting C0026780 Mumps HSDN C0016382 Cutaneous vascular engorgement C0032339 Rothmund-thomson syndrome OrphaNet|MalaCards C0031911 Pigment deposition C3896578 Familial colorectal cancer type x MalaCards C4084766 Vomiting C0085278 Antiphospholipid syndrome HSDN C4084788 Have dizziness C0040128 Thyroid diseases HSDN C3641756 Have diarrhea C0014394 Enuresis HSDN C0002962 Angina C0040409 Tongue diseases HSDN C1963184 Nystagmus adverse event C0342871 Acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0006663 Calcinosis HSDN C0030975 Disorders perception C0001940 Alcohol amnestic disorder HSDN C3887638 Failure to thrive in infant C0023176 Lead poisoning MalaCards C0034933 Abnormal reflexes C0025183 Meige syndrome HSDN C1963281 Vomiting adverse event C0162671 Melas syndrome HSDN C0018524 Hallucinate C2984289 Melanoma pathway HSDN C3641756 Have diarrhea C0035637 Rinderpest HSDN C1963091 Diarrhea adverse event C0026785 Munchhausen syndrome HSDN C0015672 Decreased energy C1336011 Postgerminal center small lymphocytic lymphoma UMLS C1557397 Adverse event associated with pain C0013806 Electroplexy shock therapy HSDN C0035229 Respiratory function impaired C1842691 Diaphanospondylodysostosis MalaCards|HPO C0018772 Deafness C0086651 Mucopolysaccharidosis, mps-iv-a OrphaNet|HPO|MalaCards C0041667 Low weight C0220765 Weaver-like syndrome MalaCards C1963067 Atrial fibrillation adverse event C3714995 Cardiomyopathy, dilated, 1kk MalaCards C0576456 Poor feeding C3810023 Verheij syndrome MalaCards C2911647 Weight gain adverse event C0518449 Control of hip fracture risk HSDN C0040264 Ear ringing sound C0024141 Lupus erythematosus, systemic HSDN C4084767 Bothered by vomiting C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0221150 Odynophagia C0001175 Acquired immunodeficiency syndrome UMLS C2024893 Cardiovascular surgery result: fatigue C0040053 Thrombosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C1557397 Adverse event associated with pain C0015671 Father HSDN C0030552 Paralysis partial C0041296 Tuberculosis HSDN C0349588 Stature short C1860789 Leukemia, megakaryoblastic, of down syndrome HPO C0917816 Deficiency mental C2931547 Kozlowski-krajewska syndrome OrphaNet|MalaCards C0155502 Vertigo benign positional C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0497406 Over weight C0002871 Anemia HSDN C0030552 Paralysis partial C0268386 Amyloid polyneuropathy, swiss type MalaCards C0007758 Cerebellar ataxia C0162666 Mitochondrial encephalomyopathies HSDN C0424755 Fever symptoms C0013990 Pathological accumulation of air in tissues HSDN C0042571 Vertigo subjective C0035460 Rhinitis, vasomotor HSDN C2029884 Hearing loss by exam C0007873 Uterine cervical neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038463 Strongyloides infection HSDN C4084727 Cough frequency C0028433 Nose neoplasms HSDN C0518090 Frequency of pain question C0003614 Appendiceal neoplasms HSDN C0018834 Brash C0023895 Liver diseases HSDN C0030200 Intractable pain C0262593 Injury nerve peripheral HSDN C4085211 Pain distress question C0282607 Vascular neoplasms HSDN C4084776 Weight loss C0013502 Echinococcosis HSDN C1384666 Decreased hearing C0027697 Nephritis HSDN C0036572 Convulsion C0342443 Adrenal cushing's syndrome HSDN C0184567 Pain acute C0029928 Ovarian diseases HSDN C0034155 Thrombotic thrombocytopenic purpura C0011633 Dermatomyositis HSDN C0518090 Frequency of pain question C1552527 Clinic / center - developmental disabilities HSDN C4085210 Usual severity pain C0021833 Intestinal fistula HSDN C0013395 Indigestion C0019196 Hepatitis c HSDN C0221232 Welts C1304197 Urticaria secondary to infection UMLS C4085222 Nausea C0005940 Bone diseases HSDN C0016382 Cutaneous vascular engorgement C0026948 Mycosis fungoides MalaCards C0012833 Dizzy C0027947 Neutropenia HSDN C0233844 Awkwardness C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C0233514 Behavior abnormal C0162565 Acute intermittent porphyria OrphaNet|MalaCards C2029884 Hearing loss by exam C0023467 Leukemia, myelocytic, acute HSDN C3539023 Pelvic pain increasing in frequency C0009375 Colonic neoplasms HSDN C3887638 Failure to thrive in infant C1706004 Anhydrotic ectodermal dysplasias MalaCards C4084723 Constipation C1739094 Foodborne botulism OrphaNet|MalaCards C0557874 Global developmental delay C1845167 Dent disease 2 MalaCards|HPO C0030232 Color loss C0242342 Sheehan syndrome OrphaNet|MalaCards C0232462 Appetite decrease C2239176 Liver carcinoma MalaCards C4085211 Pain distress question C0001818 Agoraphobia HSDN C0009676 Confusion state C0043251 Wounds and injuries HSDN C0018681 Headache, cephalalgia C1333598 Fap associated medulloblastoma UMLS C0085593 Chill C0006309 Brucellosis HSDN C3887638 Failure to thrive in infant C1849435 Bicarbonate-wasting rta OrphaNet|HPO C0018681 Headache, cephalalgia C1711278 Nasopharyngeal papillary adenocarcinoma UMLS C0004134 Dyssynergia C0014553 Absence epilepsy HSDN C3641755 Have constipation C0085073 Prosthesis-related infection HSDN C0004134 Dyssynergia C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO|UMLS C4085661 Usual severity nausea C0002994 Angioedema HSDN C1549543 Administration method - pain C0011981 Diaphragmatic eventration HSDN C4084775 Usual severity weight loss C0262655 Recurrent urinary tract infection HSDN C3898969 Have been vomiting C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C3146279 Coma C0342257 Complications of diabetes mellitus HSDN C1963137 Hydrocephalus adverse event C1850055 Peho syndrome OrphaNet|HPO|MalaCards C3539896 Pelvic pain occurs with urination C0020517 Hypersensitivity HSDN C2203646 Jaundice C0003492 Aortic coarctation HSDN C1963180 Neck pain adverse event C0752155 Central nervous system vascular malformations HSDN C4084725 Usual severity cough C2937421 Prostatic hyperplasia HSDN C0242670 Chronic vegetative state C0034065 Pulmonary embolism HSDN C2203646 Jaundice C0393591 Aicardi-goutieres syndrome HPO C1963184 Nystagmus adverse event C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C0151825 Ostalgia C1850568 Nakajo syndrome MalaCards|HPO|UMLS C0009806 Constipate C0600260 Lung diseases, obstructive HSDN C2024878 Cardiovascular surgery result: dyspnea C4042784 Feeding and eating disorders HSDN C2911645 Weight loss adverse event C0039538 Teratoma HSDN C2032395 Pelvic pain on the left C0004275 Attitude health HSDN C0018524 Hallucinate C0002871 Anemia HSDN C0013595 Eczematous dermatitis C3661525 Autosomal recessive chronic granulomatous disease MalaCards C0424755 Fever symptoms C0023364 Leptospirosis DiseaseOntology|MalaCards C3539889 Pelvic pain increasing in severity C1550672 Specimen type - ulcer HSDN C3898969 Have been vomiting C0017601 Glaucomas HSDN C4084767 Bothered by vomiting C0019054 Hemolysis (disorder) HSDN C1549543 Administration method - pain C0473583 Nevus elasticus HSDN C3539020 Pelvic pain decreasing in frequency C1456865 Ureteral calculi HSDN C0027497 Queasy C0023343 Leprosy HSDN C0086565 Liver function abnormal C0748400 Rh disease MalaCards C0020507 Abnormal enlargement of an organ or a tissue C3808953 Nephrotic syndrome, type 8 MalaCards C2138385 Craving laundry starch C0031873 Pica disease UMLS C0042024 Urine incontinence C0017636 Glioblastoma HSDN C0024031 Back pain lower back C0040046 Thrombophlebitis HSDN C0424755 Fever symptoms C0085652 Pyoderma gangrenosum OrphaNet|MalaCards C0036572 Convulsion C0023795 Lipoid proteinosis of urbach and wiethe HPO|UMLS C0700078 Deep tendon reflex decrease C1838979 Mitochondrial complex i deficiency MalaCards|HPO C0000737 Abdomen pain C3272465 Ampulla of vater invasive papillary adenocarcinoma UMLS C0021359 Infertility C0272052 Rh deficiency syndrome MalaCards C4085210 Usual severity pain C0085078 Lysosomal storage diseases HSDN C4084723 Constipation C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0030794 Pelvis pain C0282606 Myomatous neoplasm HSDN C1962972 Proteinuria adverse event C0023241 Legionnaires' disease MalaCards C0004604 Pain back C1552262 Nurse practitioner - family HSDN C0004134 Dyssynergia C0085084 Motor neuron disease HSDN C0026821 Cramp C0007760 Cerebellar diseases HSDN C4085317 Diarrhea frequency C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C4084769 Vomiting frequency C0036357 Psychology, schizophrenic HSDN C0040822 D tremors C0006112 Brain diseases, metabolic HSDN C0557874 Global developmental delay C0342871 Acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0231218 Malaise generalized C1335979 Extrahepatic bile duct small cell nec UMLS C3641756 Have diarrhea C1258104 Diffuse scleroderma HSDN C3641755 Have constipation C0268328 Porphobilinogen synthase deficiency MalaCards C0019825 Voice hoarseness C0085653 Pyogenic granuloma HSDN C0018991 Paralysis one side of body C0027666 Neoplasms, radiation-induced HSDN C0036572 Convulsion C1868690 Hypoadrenocorticism, familial UMLS C0018681 Headache, cephalalgia C0038362 Stomatitis HSDN C0020673 Hypothermia (central) (local) C0040128 Thyroid diseases HSDN C2096293 Ent surgical result ear vertigo C0027859 Acoustic neuroma OrphaNet|HPO C0152116 Torticollis spasmodic C1851920 Dopa-responsive dystonia HPO C4085317 Diarrhea frequency C0003864 Arthritis HSDN C4085211 Pain distress question C0016558 Forensic psychiatri HSDN C1384666 Decreased hearing C0011875 Diabetic angiopathies HSDN C0022107 Fussiness C0023521 Globoid cell leukodystrophy OrphaNet C4085210 Usual severity pain C0035854 Rosacea HSDN C1962972 Proteinuria adverse event C2004491 Cicatrix HSDN C2911645 Weight loss adverse event C0236664 Alcohol-related disorders HSDN C0221263 Cafe au lait spot C0002989 Epithelioid hemangioma of skin HSDN C2185938 Loss of interest or pleasure C0178417 Anhedonia UMLS C0151786 Weakness muscle C0162671 Melas syndrome OrphaNet|HPO|MalaCards C3714552 Strength decreased C2677843 Episodic ataxia, type 7 MalaCards|UMLS C0027066 Myoclonic jerking C3151959 Renal tubulopathy, diabetes mellitus, and cerebellar ataxia UMLS C0036572 Convulsion C1720983 Channelopathies HSDN C1705500 Flasher - visual manifestation C0346388 Malignant melanoma of choroid HPO C0344370 Posset C1504321 Infantile spitting up UMLS C0036572 Convulsion C0206138 Crest syndrome MalaCards C3815497 Cough C0700595 Spinal muscular atrophies of childhood HSDN C1962957 Flushing adverse event C0014548 Epilepsy, generalized HSDN C0002962 Angina C0086795 Pfaundler-hurler syndrome HPO C0040259 Tinea pedis C0013182 Drug allergy HSDN C0004604 Pain back C2586211 Thrombosis of blood vessel HSDN C0917816 Deficiency mental C1855243 Metaphyseal acroscyphodysplasia OrphaNet|MalaCards C0015672 Decreased energy C0023241 Legionnaires' disease OrphaNet|MalaCards C0037384 Snore C0029456 Osteoporosis HSDN C0013395 Indigestion C0037199 Sinusitis HSDN C4085222 Nausea C0518450 Spinal fractures HSDN C1579931 Depressed - symptom C1868681 Dystonia 12 HPO C0016382 Cutaneous vascular engorgement C0263428 Burnett schwartz berberian syndrome MalaCards C1549543 Administration method - pain C1705812 Nci thesaurus role HSDN C0033377 Caudal displacement C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C1963281 Vomiting adverse event C0032987 Ectopic pregnancy HSDN C4085642 Level of joint stiffness C0814154 Alcohol-related neurodevelopmental disorder OrphaNet|MalaCards C0013911 Emaciate C0003838 Arterial occlusive diseases HSDN C2032396 Pelvic pain on the right C0005491 Biofeedback HSDN C2024893 Cardiovascular surgery result: fatigue C0034065 Pulmonary embolism HSDN C3665492 Pigmentations C0334444 Spindle cell melanoma MalaCards C0010520 Skin cyanosis C0023418 Leukemia HSDN C0013428 Painful urination C1336450 Stage i bladder urothelial carcinoma UMLS C0747556 Pharyngitis recurrent C0026691 Mucocutaneous lymph node syndrome OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1090821 Sepsis (invertebrate) HSDN C1963064 Anxiety adverse event C0796237 Mental retardation, x-linked 30 HPO C0036572 Convulsion C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards|HPO C1963091 Diarrhea adverse event C0040425 Tonsillitis HSDN C2911647 Weight gain adverse event C0041234 Chagas disease HSDN C0011991 Loose stools C0026266 Mitral valve insufficiency HSDN C0018926 Emesis bloody C0038454 Cerebrovascular accident HSDN C1963091 Diarrhea adverse event C0348018 Projections HSDN C3898969 Have been vomiting C0003838 Arterial occlusive diseases HSDN C0151686 Growth retardation C3553637 Hyperphosphatasia with mental retardation syndrome 2 MalaCards C4085317 Diarrhea frequency C0035358 Retroperitoneal neoplasm HSDN C4084767 Bothered by vomiting C1855116 Methylmalonic aciduria, mut(-) type HPO C0027497 Queasy C0038160 Staphylococcal infections HSDN C0006370 Bulimia C0037361 Olfactory sense HSDN C0151786 Weakness muscle C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards|UMLS C4084784 Diarrhea C0023420 Mouse leukemia l1210 HSDN C4050613 Anxiety C3280358 Wolfram-like syndrome, autosomal dominant OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0268680 Biotin deficiency MalaCards C0000737 Abdomen pain C1005359 Pica pica bird HSDN C0018772 Deafness C0018188 Granuloma HSDN C2984058 Have pain C0003466 Anus, imperforate HSDN C0011991 Loose stools C1846171 Lissencephaly, x-linked, 2 HPO C0030193 Sense of pain C0358297 Anthrax vaccines HSDN C0043094 Weight gain C0241158 Cicatrix skin HSDN C2029884 Hearing loss by exam C1956097 Wolf-hirschhorn syndrome MalaCards C4084768 Usual severity vomiting C0024535 Malaria, falciparum HSDN C1971624 Appetite absent C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C3815497 Cough C0205969 Thymic carcinoma OrphaNet|MalaCards C4084784 Diarrhea C0040558 Toxoplasmosis HSDN C0013421 Dystonia C0010054 Coronary arteriosclerosis HSDN C0018834 Brash C0796003 Juberg-marsidi syndrome HPO C2984058 Have pain C1968835 Egot gene HSDN C0022107 Fussiness C0268255 Farber lipogranulomatosis MalaCards C0013421 Dystonia C1859807 Amyotrophic lateral sclerosis 2, juvenile (disorder) MalaCards|HPO C3665347 Vision impaired C0265962 Ichthyosis linearis circumflexa MalaCards C0015672 Decreased energy C0340951 Erythrogenesis imperfecta MalaCards C4085210 Usual severity pain C0033944 Psychosexual development HSDN C0231835 Respiration rate increased C1968602 Surfactant metabolism dysfunction, pulmonary, 1 MalaCards|HPO C0022346 Yellow skin C0010340 Critical illness HSDN C1557397 Adverse event associated with pain C0002880 Autoimmune hemolytic anemia HSDN C3146279 Coma C0038379 Eye deviation HSDN C4084784 Diarrhea C0027868 Neuromuscular diseases HSDN C2032395 Pelvic pain on the left C0007860 Uterine cervicitis HSDN C4084775 Usual severity weight loss C1561518 Pleasure - animals raised for recreation HSDN C1961131 Cough adverse event C0030286 Pancreatic diseases HSDN C0043094 Weight gain C0019054 Hemolysis (disorder) HSDN C0015469 Facial paralysis C3887662 Intraspinal neoplasm HSDN C0035229 Respiratory function impaired C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards C0010200 Cough symptom C1708765 Lung adenocarcinoma, mixed subtype UMLS C0035229 Respiratory function impaired C1843633 Myopathy, distal, with early respiratory failure, autosomal dominant MalaCards C0085635 Flash light C0220633 Uveal melanoma HPO C0240715 Perineal lump C0559487 Paratesticular tumor UMLS C2919142 Short stature adverse event C0023786 Mucopolysaccharidosis i OrphaNet C0575081 Abnormal gait C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0020505 Excessive eating C0221032 Familial generalized lipodystrophy MalaCards C0011991 Loose stools C2239176 Liver carcinoma MalaCards C3829611 Nausea frequency C0017150 Gastrinoma OrphaNet|MalaCards C0424755 Fever symptoms C3645711 Congenital osteopetrosis MalaCards C2242996 Tingling C3665624 Serum calcium below normal HSDN C0042798 Vision dim C1845407 Cone-rod dystrophy, x-linked, 3 HPO C0036572 Convulsion C3146222 Idiopathic aortitis MalaCards C4084788 Have dizziness C1457883 Aggressive reaction HSDN C0002962 Angina C0019284 Diaphragmatic hernia HSDN C0018772 Deafness C1963282 Wolff-parkinson-white syndrome adverse event HSDN C2024878 Cardiovascular surgery result: dyspnea C0021833 Intestinal fistula HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043541 Zygomycoses HSDN C0010200 Cough symptom C0810021 Other lower respiratory disease UMLS C0019209 Large liver C3887654 Polyarteritis nodosa, childhood-onset MalaCards C0033774 Skin pruritus C3827868 Tachycardia by ecg finding HSDN C1961131 Cough adverse event C1532560 Plasmacytoma - category HSDN C2984058 Have pain C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C0030794 Pelvis pain C1963088 Cystitis adverse event HSDN C4085317 Diarrhea frequency C0206172 Diabetic foot HSDN C1557397 Adverse event associated with pain C0018051 Gonadal dysgenesis HSDN C0007758 Cerebellar ataxia C0439840 Reflex motion descriptor HSDN C2911645 Weight loss adverse event C0023290 Leishmaniasis, visceral DiseaseOntology C3815497 Cough C0028796 Dermatitis, occupational HSDN C3641756 Have diarrhea C0029401 Osteitis deformans HSDN C3898969 Have been vomiting C0016483 Food preferences HSDN C0042571 Vertigo subjective C0027627 Neoplasm metastasis HSDN C0012833 Dizzy C0026782 Mumps vaccine HSDN C0036572 Convulsion C0035435 Rheumatism HSDN C0085632 Listlessness C2717757 Retinocochleocerebral vasculopathies MalaCards C4085661 Usual severity nausea C0015397 Disorder of eye HSDN C0015469 Facial paralysis C1832370 Myopathy, myofibrillar, desmin-related MalaCards|HPO C0018681 Headache, cephalalgia C0034882 Rectal diseases HSDN C0013604 Edematous C1522133 High cholesterol level HSDN C0231807 Dyspnea exertional C0272118 Warm autoimmune hemolytic anemia OrphaNet|MalaCards C0009792 Consciousness disorder C0014557 Epilepsy, post-traumatic HSDN C0042571 Vertigo subjective C0001973 Alcoholic intoxication, chronic HSDN C0151786 Weakness muscle C1449844 Pseudohypoaldosteronism, type ii MalaCards C0035078 Failure kidney C1865794 Rhyns syndrome MalaCards C3146279 Coma C0002792 Anaphylaxis HSDN C1963087 Constipation adverse event C1005359 Pica pica bird HSDN C4085548 Usual severity dizziness C0032914 Pre-eclampsia HSDN C2242996 Tingling C0016658 Fracture bone HSDN C1384666 Decreased hearing C0376175 Bell palsy HSDN C0043094 Weight gain C0020545 Hypertension, renovascular HSDN C2919142 Short stature adverse event C0268238 Triglyceride storage disease with ichthyosis MalaCards C0000737 Abdomen pain C1335398 Gastric peutz-jeghers polyp MalaCards C1963281 Vomiting adverse event C0038000 Spleen rupture HSDN C4085661 Usual severity nausea C0030568 Parkinsonism, postencephalitic HSDN C1000483 Genus anemia C2673610 Jeb-i MalaCards C0020672 Body temperature decreased C0026640 Mouth neoplasms HSDN C0004134 Dyssynergia C0022340 Late-infantile neuronal ceroid lipfuscinosis OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C3714514 Infection HSDN C1963086 Confusion adverse event C2931384 Moyamoya disease 1 HSDN C0751495 Seizure focal C0598392 Lennox syndrome MalaCards C2984057 Have nausea C0036357 Psychology, schizophrenic HSDN C0003469 Anxiety disorder C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C4084767 Bothered by vomiting C0268151 Classical galactosemia MalaCards|HPO C0557874 Global developmental delay C1845408 Contiguous abcd1-dxs1375e deletion syndrome MalaCards|HPO C1971624 Appetite absent C0011989 Camurati-engelmann syndrome MalaCards|HPO C0030193 Sense of pain C0031485 Phenylketonurias HSDN C0034933 Abnormal reflexes C0009197 Cochlear diseases HSDN C0023380 Lethargy C0206687 Carcinoma, endometrioid HSDN C0020458 Hyperhydrosis C2931923 Hyperkeratosis of the palms and soles and esophageal papillomas MalaCards C0020505 Excessive eating C0001726 Affective symptoms HSDN C0036396 Sciatica C0003873 Rheumatoid arthritis HSDN C0027497 Queasy C0003838 Arterial occlusive diseases HSDN C4084724 Usual severity constipation C1548484 Rheumatic fever vaccine HSDN C0241165 Skin thickening C1855477 Dahlberg borer newcomer syndrome OrphaNet|MalaCards C0848203 Male pelvic pain C0206654 Leiomyomatosis HSDN C0518090 Frequency of pain question C0029124 Optic atrophy HSDN C0220982 Keto acidosis C3280314 Combined malonic and methylmalonic aciduria MalaCards C1963137 Hydrocephalus adverse event C2936791 Antley-bixler syndrome, autosomal dominant MalaCards C4085211 Pain distress question C0015556 Fallopian tube diseases HSDN C0002965 Crescendo angina C0012644 Animal disease models HSDN C0030193 Sense of pain C0206694 Mucoepidermoid carcinoma HSDN C0004604 Pain back C0021400 Influenza HSDN C0151786 Weakness muscle C0035436 Rheumatic fever HSDN C0853241 Exacerbation of anxiety C0003467 Anxiety UMLS C4084723 Constipation C0342859 Harderoporphyria HPO C0016382 Cutaneous vascular engorgement C4053908 Late onset tylosis MalaCards C0002792 Anaphylaxis, generalized C0263610 Sunlight-induced angio-edema-urticaria MalaCards C0000737 Abdomen pain C0040127 Thyroid crisis HSDN C0242936 Center pain C0006705 Calcium metabolism disorders HSDN C0240735 Personality change C0020179 Huntington disease MalaCards|HPO|UMLS C0039870 Leanness C0018802 Congestive heart failure HSDN C0020458 Hyperhydrosis C1721006 Keratoderma, palmoplantar, epidermolytic OrphaNet|HPO|MalaCards C0000727 Abdomen acute C2984572 Malaria pathway HSDN C0017181 Gastrointestinal bleed C0546323 Inferior vena cava membranous obstruction MalaCards C0151740 Intracranial hypertension C0175699 Saethre-chotzen syndrome MalaCards|HPO C0018681 Headache, cephalalgia C1136042 Neuroma, acoustic, bilateral HPO C0026884 Muteness C0233610 Negativism in catatonia HSDN C4024607 Exercise-induced leg cramps C3888109 Acromelalgia hereditary MalaCards C0033774 Skin pruritus C1333081 Colloid carcinoma of the pancreas UMLS C0019079 Bloody sputum C1336209 Stage iiia large cell carcinoma of lung UMLS C0013395 Indigestion C0014852 Esophageal diseases HSDN C0039231 Heartbeats increased C1854336 Paragangliomas 3 MalaCards|HPO C0270795 Monopareses C1290877 Extremities disorders UMLS C3887873 Hearing loss C0025292 Haemophilus meningitis HSDN C0036396 Sciatica C0042345 Varicosity HSDN C3146279 Coma C0032326 Pneumothorax HSDN C0013604 Edematous C0032229 Pleural neoplasms HSDN C3641756 Have diarrhea C0001627 Congenital adrenal hyperplasia HSDN C1963252 Tremor adverse event C0004239 Atrial flutter HSDN C0036572 Convulsion C0796154 Simpson-golabi-behmel syndrome, type 1 MalaCards|HPO C0010200 Cough symptom C0031117 Peripheral neuropathy HSDN C3815497 Cough C0236969 Substance-related disorders HSDN C1963091 Diarrhea adverse event C0014849 Esophageal and gastric varices HSDN C3887873 Hearing loss C0026848 Myopathy HSDN C4042891 Sleep wake disorders C0013363 Dysautonomia HSDN C2984058 Have pain C1302808 Myopericytoma HSDN C0587051 Lumbar mass C0684559 Benign neop. lumbar vertebra UMLS C0040264 Ear ringing sound C0037198 Sinus thrombosis, intracranial HSDN C3541349 Syncope C1579931 Depressed - symptom HSDN C2237041 Shox gene with short stature C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0011570 Monopolar depression C1858496 Advanced sleep-phase syndrome, familial HPO C0020538 Hbp C1852456 Cryoglobulinemia, familial mixed MalaCards C0007166 Cardiac output decreased C0001973 Alcoholic intoxication, chronic HSDN C0234132 Pyramidal sign C0085209 Bovine spongiform encephalitis MalaCards C0018777 Deafness, conductive C1962979 Burn adverse event HSDN C0011206 Delirium acute C0037369 Smoking HSDN C0042798 Vision dim C0206178 Cytomegalovirus retinitis HSDN C4084774 Have weight loss C3489413 Lipomatosis, multiple HSDN C0015672 Decreased energy C0032066 Plague vaccines HSDN C3815497 Cough C0001486 Adenovirus infections HSDN C0020615 Hypoglycemia nos C0268600 3-methylcrotonyl coa carboxylase 1 deficiency OrphaNet|HPO|MalaCards C0011991 Loose stools C1833053 Proprotein convertase 1 3 deficiency HPO|UMLS C4084775 Usual severity weight loss C0036118 Salmonella infections, animal HSDN C0011991 Loose stools C0020473 Hyperlipidemia HSDN C3887638 Failure to thrive in infant C1956125 Alagille syndrome 1 HPO C0009792 Consciousness disorder C0003873 Rheumatoid arthritis HSDN C3665346 Loss sight C0039483 Giant cell arteritis MalaCards|HPO C0016382 Cutaneous vascular engorgement C0398368 Lymphatic abnormalities HSDN C2024893 Cardiovascular surgery result: fatigue C0034734 Raynaud disease HSDN C0034150 Skin purpura C0003869 Arthritis, infectious HSDN C2911645 Weight loss adverse event C0406645 Amyopathic dermatomyositis MalaCards C4084897 Sleep disturbance subordinate domain C2931673 Ceroid lipofuscinosis, neuronal 1, infantile MalaCards|HPO C4084774 Have weight loss C0033906 Psychological theories HSDN C1963091 Diarrhea adverse event C0036916 Sexually transmitted diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018916 Hemangioma HSDN C0242936 Center pain C0020119 Human development HSDN C1963137 Hydrocephalus adverse event C1959582 Pten hamartoma tumor syndrome MalaCards C0036572 Convulsion C0026706 Mucopolysaccharidosis iii OrphaNet|MalaCards C2203646 Jaundice C0002892 Anemia, pernicious HSDN C0018772 Deafness C3151476 Mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MalaCards|HPO C0042963 Symptoms vomiting C0002949 Aneurysm, dissecting HSDN C2315100 Pediatric failure to thrive C1956097 Wolf-hirschhorn syndrome OrphaNet|HSDN|HPO|MalaCards C0850758 Pain pelvic C0037051 Behavior illness HSDN C4082202 Sleep quality question C0022336 Creutzfeldt-jakob disease MalaCards C0028738 Nystagmus C3150802 Myopathy, lactic acidosis, and sideroblastic anemia 2 MalaCards|HPO C0575081 Abnormal gait C0268595 Glutaric aciduria, type 1 HPO C0013404 Respiratory difficulty C0001824 Agranulocytosis HSDN C2315100 Pediatric failure to thrive C0432328 Xeroderma pigmentosum, variant form MalaCards C0349506 Sun sensitivity C0751785 Unverricht-lundborg syndrome MalaCards|HPO C4084725 Usual severity cough C0031090 Periodontal diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0033923 Psychomotor function HSDN C0016382 Cutaneous vascular engorgement C0432306 Ichthyosis bullosa of siemens MalaCards C0522224 Palsied C0007133 Carcinoma, papillary HSDN C0013404 Respiratory difficulty C0011854 Diabetes mellitus, insulin-dependent HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0038395 Streptococcal infections HSDN C0009676 Confusion state C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C0005745 Blepharoptosis C2931557 Chromosome 4 short arm deletion MalaCards C0027796 Neuralgias C1258104 Diffuse scleroderma HSDN C4020887 Photodysphoria C1562113 Fleck corneal dystrophy HPO C2911647 Weight gain adverse event C0004623 Bacterial infections HSDN C3665492 Pigmentations C0006118 Brain neoplasms MalaCards C1549543 Administration method - pain C0021841 Intestinal neoplasms HSDN C3539890 Pelvic pain causes awakening at night C1552262 Nurse practitioner - family HSDN C0013421 Dystonia C0003873 Rheumatoid arthritis HSDN C0009806 Constipate C3665349 Secondary hypothyroidism OrphaNet|MalaCards C0424755 Fever symptoms C0037944 Spinal stenosis HSDN C2024893 Cardiovascular surgery result: fatigue C1858361 Pyogenic arthritis, pyoderma gangrenosum and acne OrphaNet|HPO|MalaCards C1279888 Proteinuria of undiagnosed cause C0018799 Heart diseases HSDN C3887873 Hearing loss C0037579 Soft tissue neoplasms HSDN C0518090 Frequency of pain question C0018923 Hemangiosarcoma HSDN C0577572 Mass of musculoskeletal structure C2919808 Cholesterin granuloma of middle ear and mastoid UMLS C0518090 Frequency of pain question C0005690 Bladder fistula HSDN C0240715 Perineal lump C0030849 Penile neoplasms UMLS C1963281 Vomiting adverse event C0029132 Disorder of the optic nerve HSDN C0151786 Weakness muscle C0007286 Carpal tunnel syndrome HSDN C3539889 Pelvic pain increasing in severity C1704436 Peripheral arterial diseases HSDN C0018681 Headache, cephalalgia C0037579 Soft tissue neoplasms HSDN C4042891 Sleep wake disorders C0032914 Pre-eclampsia HSDN C2203646 Jaundice C0013902 Elliptocytosis, hereditary HSDN C1963087 Constipation adverse event C0003873 Rheumatoid arthritis HSDN C1384666 Decreased hearing C3553937 Pbd4b MalaCards C4084763 Frequency of shortness of breath C0004096 Asthma DiseaseOntology|MalaCards C0577569 Mass of male genital structure C0347000 Metastatic malignant neoplasm to male genital organ, nos UMLS C2911647 Weight gain adverse event C1963274 Vasculitis adverse event HSDN C4085211 Pain distress question C0013712 Ego HSDN C0028081 Night sweat C0279540 Hd ld, adult UMLS C2911647 Weight gain adverse event C1962986 Glaucoma adverse event HSDN C0000731 Abdomen distention C1334818 Multicystic mesothelioma of peritoneum MalaCards C2024893 Cardiovascular surgery result: fatigue C1962971 Myocarditis adverse event HSDN C4084725 Usual severity cough C2936664 Acquired hypogammaglobulinemia HSDN C3887873 Hearing loss C1849112 Spastic quadriplegia-retinitis pigmentosa-mental retardation syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0009862 Contraception behavior HSDN C4084784 Diarrhea C0040948 Trichostrongyliasis HSDN C3815497 Cough C0032298 Lipid pneumonia HSDN C3641756 Have diarrhea C0030283 Pancreatic cyst HSDN C1090821 Sepsis C0155866 Inhalational anthrax OrphaNet|MalaCards C0018784 Deafness sensorineural C0009240 Cognition HSDN C4084766 Vomiting C0001584 Adolescent psychology HSDN C0002962 Angina C0018824 Heart valve disease HSDN C1963252 Tremor adverse event C0265499 49,xxxxy chromosomal anomaly MalaCards C0007758 Cerebellar ataxia C2749345 Refsum disease, adult, 1 HPO C2984058 Have pain C0158266 Intervertebral disc degeneration HSDN C1549543 Administration method - pain C0042582 Vesicovaginal fistula HSDN C0019214 Hepatosplenomegaly C0153459 Malignant neoplasm of body of pancreas MalaCards C3829611 Nausea frequency C0041318 Tuberculosis, meningeal HSDN C0015672 Decreased energy C1333044 Cmml-2 UMLS C0020580 Decreased sensation C2350522 Touch perception HSDN C0009676 Confusion state C0026961 Mydriasis HSDN C2032395 Pelvic pain on the left C0040136 Thyroid neoplasm HSDN C2242996 Tingling C0014121 Bacterial endocarditis HSDN C0423773 Skin scaly C1836669 Congenital disorder of glycosylation, type if MalaCards|UMLS C0003550 Broca aphasia C1999266 Depression adverse event HSDN C4085210 Usual severity pain C0035042 Psychology and religion HSDN C0034124 Pupillary disorder C0027651 Tumor HSDN C0020672 Body temperature decreased C2239176 Liver carcinoma HSDN C0013604 Edematous C0039538 Teratoma HSDN C1549543 Administration method - pain C0376547 Aromatherapy HSDN C1145670 Failure respiratory C1836050 Filaminopathy, autosomal dominant MalaCards|HPO C0036572 Convulsion C0040961 Tricuspid valve insufficiency HSDN C0206146 Myocardial stunning C0004096 Asthma HSDN C4084767 Bothered by vomiting C0023176 Lead poisoning MalaCards C0476273 Distress respiratory C0340427 Familial dilated cardiomyopathy MalaCards C0850758 Pain pelvic C0012746 Dissociative disorder HSDN C0518090 Frequency of pain question C0034040 Puerperal disorders HSDN C0086439 Activity decreased C0456892 Csf low pressure HSDN C4084769 Vomiting frequency C0870082 Hyperkeratosis HSDN C0013428 Painful urination C0010153 Corynebacterium infections HSDN C3539892 Pelvic pain in front C1704436 Peripheral arterial diseases HSDN C0040264 Ear ringing sound C1837218 Cleft palate, isolated HSDN C0557874 Global developmental delay C1844887 Catel manzke syndrome MalaCards C0035229 Respiratory function impaired C0011633 Dermatomyositis OrphaNet|MalaCards C0011991 Loose stools C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0745966 Lower leg edema C0577685 Gravitational edema of leg UMLS C4085211 Pain distress question C0037304 Skull fracture HSDN C4084767 Bothered by vomiting C0151526 Premature birth HSDN C1557397 Adverse event associated with pain C0206704 Carcinoma, large cell HSDN C3641756 Have diarrhea C0023343 Leprosy HSDN C0333274 Purulent discharge C0521772 Ear discharge purulent UMLS C0242936 Center pain C0027070 Myoepithelioma HSDN C0242936 Center pain C0149520 Acute cholecystitis HSDN C3829611 Nausea frequency C1321581 Bezoar disorder HSDN C0030193 Sense of pain C0041755 Adverse reaction to drug HSDN C0035232 Diaphragmatic paralysis C0010054 Coronary arteriosclerosis HSDN C0039870 Leanness C0002871 Anemia HSDN C1963137 Hydrocephalus adverse event C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C0221166 Paraparesis C0085084 Motor neuron disease HSDN C1963170 Hypothermia adverse event C1269683 Major depressive disorder HSDN C0030200 Intractable pain C0038160 Staphylococcal infections HSDN C0030193 Sense of pain C0015408 Eye injury HSDN C0020455 Hypergammaglobulinemia C0037299 Skin ulcer HSDN C0034150 Skin purpura C0398625 Protein c deficiency OrphaNet|HPO|MalaCards C0241137 Skin pallor C0267370 Angiodysplasia of colon HSDN C1557397 Adverse event associated with pain C0015959 Fetomaternal bleeding HSDN C1963064 Anxiety adverse event C2936346 22q11 deletion syndrome MalaCards|HPO C0240715 Perineal lump C0742136 Cervical condyloma UMLS C0009806 Constipate C0007784 Cerebral hemisphere hemorrhage HSDN C0349588 Stature short C1866504 Photosensitive trichothiodystrophy MalaCards|HPO C0000737 Abdomen pain C1518871 Pancreatic intraductal papillary mucinous neoplasm with an associated invasive carcinoma UMLS C0030193 Sense of pain C0004763 Barrett esophagus HSDN C3539022 Pelvic pain decreasing in severity C0011854 Diabetes mellitus, insulin-dependent HSDN C0007758 Cerebellar ataxia C0016542 Foreign body HSDN C2984057 Have nausea C0031511 Pheochromocytoma MalaCards C0000737 Abdomen pain C3273019 Early hepatocellular carcinoma UMLS C4084727 Cough frequency C0042133 Uterine fibroids HSDN C4085317 Diarrhea frequency C3463824 Myelodysplastic syndrome HSDN C4085862 Bothered by nausea C0021818 Intervertebral disk displacement HSDN C0851578 Disorder sleep C0525042 Feeding and eating disorders of childhood HSDN C0036572 Convulsion C0016169 Pathologic fistula HSDN C1963242 Stomach pain adverse event C1998095 Epizootic lymphangitis MalaCards C1549543 Administration method - pain C0040948 Trichostrongyliasis HSDN C0012569 Double vision C3887678 Cpnet MalaCards C0037199 Sinus infection C0022521 Kartagener syndrome HPO C0013405 Dyspnea, paroxysmal C0025299 Meningocele HSDN C0004134 Dyssynergia C4014371 Immunodeficiency 23 MalaCards|UMLS C0036572 Convulsion C0001125 Acidosis, lactic HSDN C1963065 Apnea adverse event C0314657 Genetic predisposition HSDN C0009421 Comatose C0677607 Hashimoto disease HSDN C0349489 Fetal hypoxia C0453996 Tobacco smoking HSDN C1963087 Constipation adverse event C0022758 Kap HSDN C1279888 Proteinuria of undiagnosed cause C0795949 Galloway mowat syndrome OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0041188 Pyomyositis, tropical HSDN C0007166 Cardiac output decreased C0041022 Pulmonary valve, stenosis, with patent foramen ovale HSDN C4084768 Usual severity vomiting C0004935 Animal ethology HSDN C4085862 Bothered by nausea C0020179 Huntington disease HSDN C0018524 Hallucinate C1862937 Ftdals1 MalaCards|HPO C0002963 Angina variant C0020538 Hypertensive disease HSDN C4020887 Photodysphoria C0339273 Corneal dystrophy, lattice type 3 MalaCards|HPO C0018784 Deafness sensorineural C0024636 Malocclusion HSDN C0020458 Hyperhydrosis C0011859 Lipoatrophic diabetes mellitus OrphaNet|HPO C2237041 Shox gene with short stature C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C3463815 Feel fatigue C1299919 Enteric coccidiosis HSDN C0751495 Seizure focal C3809624 Epileptic encephalopathy, early infantile, 18 MalaCards|UMLS C2024878 Cardiovascular surgery result: dyspnea C0023518 Leukocytosis HSDN C0026838 Spasticity muscle C1847843 Episodic ataxia, type 4 MalaCards|UMLS C4085210 Usual severity pain C0006060 Boutonneuse fever HSDN C3463815 Feel fatigue C0006118 Brain neoplasms HSDN C0013395 Indigestion C0282550 Persian gulf syndrome HSDN C0860603 Anxiety symptom C0001231 Acth syndrome, ectopic MalaCards C0522224 Palsied C0023473 Myeloid leukemia, chronic HSDN C1963091 Diarrhea adverse event C1269683 Major depressive disorder HSDN C0012569 Double vision C0037286 Skin neoplasms HSDN C0020455 Hypergammaglobulinemia C0242310 Igm heavy chain disease OrphaNet|MalaCards C0018926 Emesis bloody C4085311 Depression - recess HSDN C0019572 Hairiness C2984299 Asthma pathway HSDN C0034933 Abnormal reflexes C0151744 Myocardial ischemia HSDN C4084726 Distress cough C0153413 Malignant neoplasm of upper third of esophagus MalaCards C0015230 Exanthem C0276289 Zika virus infection MalaCards C0424755 Fever symptoms C0268307 Conjugated hyperbilirubinemia MalaCards C0040264 Ear ringing sound C2981150 Uranostaphyloschisis HSDN C0086565 Liver function abnormal C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0231528 Muscle pain generalized C0554636 Canicola fever MalaCards C0036572 Convulsion C3662034 Intractable partial temporal lobe epilepsy with impairment of consciousness UMLS C4042891 Sleep wake disorders C0035220 Respiratory distress syndrome, newborn HSDN C1963167 Memory impairment adverse event C0025286 Meningioma MalaCards C0518090 Frequency of pain question C0206647 Dermatofibrosarcoma HSDN C3641755 Have constipation C0038454 Cerebrovascular accident HSDN C1557397 Adverse event associated with pain C0242973 Ventricular dysfunction HSDN C0020672 Body temperature decreased C0340629 Aortic aneurysm without mention of rupture nos HSDN C0020672 Body temperature decreased C0018801 Heart failure HSDN C2242996 Tingling C1706377 Memory device component HSDN C0700078 Deep tendon reflex decrease C2713319 Arylsulfatase a deficiency MalaCards C0751837 Gait ataxic C0008073 Developmental disabilities HSDN C4084774 Have weight loss C3887532 Ulceration HSDN C2919142 Short stature adverse event C4014294 Desbuquois dysplasia 2 MalaCards C0030552 Paralysis partial C0020162 Humerus fracture HSDN C2024893 Cardiovascular surgery result: fatigue C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0040264 Ear ringing sound C0009240 Cognition HSDN C0013362 Dysarthrias C0153017 Encephalitis varicella HSDN C0030193 Sense of pain C0018566 Congenital hand deformities HSDN C0151827 Pain eye C0018249 Grooming HSDN C0917801 Sleep disorder insomnia C0948264 Neuroborreliosis MalaCards C0038002 Spleen enlargement C0349499 Fetal cytomegalovirus syndrome OrphaNet|MalaCards C1971624 Appetite absent C0020621 Hypokalemia HSDN C0150045 Urinary incontinence urge C0036864 Sexual relations HSDN C0030193 Sense of pain C0524851 Neurodegenerative disorders HSDN C0039070 Collapse fleeting C0474820 Glomerocytoma tympanicum HSDN C3463815 Feel fatigue C0037939 Spinal neoplasms HSDN C0151786 Weakness muscle C0026598 Movement perception HSDN C4084774 Have weight loss C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C4084775 Usual severity weight loss C0001624 Adrenal gland neoplasms HSDN C4085211 Pain distress question C0001768 Agammaglobulinemia HSDN C2984058 Have pain C0006267 Bronchiectasis HSDN C0009676 Confusion state C0040053 Thrombosis HSDN C0039070 Collapse fleeting C0008066 Child behavior disorders HSDN C0558148 Skin yellow C0151907 Discoloration of skin UMLS C3641755 Have constipation C0019159 Hepatitis a HSDN C1962972 Proteinuria adverse event C0034530 Injury radiation HSDN C0015300 Ocular proptosis C0020497 Cortical congenital hyperostosis MalaCards|HPO C0003469 Anxiety disorder C0016667 Fragile x syndrome MalaCards|HPO C0349588 Stature short C1857563 Hsd11b2, tyr299del HPO C1145670 Failure respiratory C3275954 Lacht MalaCards C0040822 D tremors C0001807 Aggressive behavior HSDN C0034933 Abnormal reflexes C1963709 Abetalipoproteinemia (lab finding) HSDN C0030200 Intractable pain C0221752 Rbc urine HSDN C0027796 Neuralgias C0024115 Lung diseases HSDN C0002622 Amnesias C1552262 Nurse practitioner - family HSDN C4084725 Usual severity cough C2706915 Language:-:point in time:^patient:- HSDN C0349588 Stature short C1563706 Nephrogenic diabetes insipidus, type ii HPO C0344232 Blurred vision C2674766 Myokymia 1 HPO C0036572 Convulsion C3551954 Coenzyme q10 deficiency, primary, 1 MalaCards|UMLS C0349588 Stature short C1843042 Craniolenticulosutural dysplasia OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C0042024 Urine incontinence C0014588 Urethral meatus, dorsal OrphaNet|MalaCards C4084784 Diarrhea C0030319 Panic disorder HSDN C4085642 Level of joint stiffness C0152441 Madelung deformity MalaCards C4084774 Have weight loss C0221752 Rbc urine HSDN C0522224 Palsied C1306794 Wound botulism MalaCards C4085317 Diarrhea frequency C0027708 Nephroblastoma HSDN C0027796 Neuralgias C3813607 Infantile gastroesophageal reflux HSDN C0030193 Sense of pain C0393834 Diabetic chronic painful polyneuropathy UMLS C3665386 Abnormal vision C1858677 Leber congenital amaurosis 3 (disorder) MalaCards|HPO C0030486 Extremity paralysis, lower C0013595 Eczema HSDN C0237849 Skin desquamation C0406355 Acrokeratosis paraneoplastica of bazex OrphaNet|MalaCards C0030794 Pelvis pain C0269185 Uterus retroverted HSDN C3539022 Pelvic pain decreasing in severity C0037313 Sleep HSDN C0233565 Bradykinesia C2931859 Acquired cjd MalaCards C1549543 Administration method - pain C0030286 Pancreatic diseases HSDN C0028738 Nystagmus C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C0000737 Abdomen pain C0037199 Sinusitis HSDN C2700617 Irritation - emotion C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C4085549 Dizziness C1258104 Diffuse scleroderma HSDN C1963086 Confusion adverse event C2984289 Melanoma pathway HSDN C0030552 Paralysis partial C0020255 Hydrocephalus HSDN C0003862 Pain joint C2931639 Macrophagic myofasciitis OrphaNet|MalaCards C0013362 Dysarthrias C1290398 Cerebral arterial aneurysm HSDN C0030193 Sense of pain C0344423 Atrial flutter by ecg finding HSDN C0151786 Weakness muscle C0751799 Brain hemorrhage, traumatic HSDN C4084776 Weight loss C0034530 Injury radiation HSDN C0042798 Vision dim C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0022346 Yellow skin C0003855 Arteriovenous fistula HSDN C1963184 Nystagmus adverse event C4015357 Mental retardation, autosomal dominant 31 MalaCards C3687298 Choanal mass C0008298 Polyp in nasopharynx UMLS C0036572 Convulsion C0024215 Lymphangiectasis, intestinal MalaCards C0011168 Disorder deglutition C0023795 Lipoid proteinosis of urbach and wiethe OrphaNet|HPO C0030193 Sense of pain C0042850 Vitamin b deficiency HSDN C0454644 Delayed language development C1968552 Mental retardation, x-linked, with spasticity HPO C1963087 Constipation adverse event C1963083 Cholecystitis adverse event HSDN C4084784 Diarrhea C0023470 Myeloid leukemia HSDN C0332573 Macula C0275746 Pintids UMLS C0008031 Pain chest C0279626 Squamous cell carcinoma of esophagus OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0280135 Germ cell tumor, mixed, ovarian UMLS C0002962 Angina C0011609 Drug eruptions HSDN C4084784 Diarrhea C0006057 Botulisms MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0001173 Adult pyloric stenosis HSDN C4084773 Bothered by weight gain C0016510 Foot diseases HSDN C3829611 Nausea frequency C0034194 Pyloric stenosis HSDN C3641756 Have diarrhea C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0242936 Center pain C0436596 On examination - apathetic HSDN C0036572 Convulsion C0393689 Non-progressive kozhevnikow syndrome UMLS C4085549 Dizziness C0162526 Aids-related opportunistic infections HSDN C0022346 Yellow skin C0268316 Cholestatic jaundice syndrome, acute UMLS C0030486 Extremity paralysis, lower C0018671 Head and neck neoplasms HSDN C0036572 Convulsion C0020459 Hyperinsulinism HSDN C0242936 Center pain C1384665 Hfe gene HSDN C4084776 Weight loss C0037397 Behavior social HSDN C0557874 Global developmental delay C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C1384666 Decreased hearing C2931258 Amaurosis congenita of leber, type 1 MalaCards C0424755 Fever symptoms C0023903 Liver neoplasms MalaCards|HSDN C0015469 Facial paralysis C0013238 Dry eye syndromes HSDN C4049644 Depression C3810230 Neurodegeneration with brain iron accumulation 6 MalaCards C0013421 Dystonia C0037769 West syndrome HSDN|HPO C0010038 Corneal opacity disorder C1859069 Brittle bone disorder OrphaNet C4085548 Usual severity dizziness C2911643 Encounter due to family history of osteoporosis HSDN C0011991 Loose stools C2239112 Blister dosing unit HSDN C0518090 Frequency of pain question C0238190 Inclusion body myositis (disorder) HSDN C0011991 Loose stools C0024668 Mammary neoplasms, experimental HSDN C0151311 Cranial nerve palsy C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0007859 Pain neck C0019080 Hemorrhage HSDN C0030552 Paralysis partial C0016124 Finger injury HSDN C0018834 Brash C0036421 Systemic scleroderma MalaCards|HSDN C0026821 Cramp C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C2237041 Shox gene with short stature C0281890 Laryngeal web OrphaNet|MalaCards C0005745 Blepharoptosis C2931107 Myasthenic syndrome, congenital, postsynaptic slow-channel MalaCards|HPO C0151786 Weakness muscle C3150973 Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degeneration and progressive polyneuropathy type) MalaCards|HPO C3898969 Have been vomiting C0023441 Leukemia, experimental HSDN C0018772 Deafness C0041234 Chagas disease HSDN C0009080 Finger clubbing C0345408 Hereditary clubbing MalaCards C3665492 Pigmentations C0206696 Carcinoma, signet ring cell MalaCards C1384666 Decreased hearing C0268390 Muckle-wells syndrome MalaCards|HPO C0036396 Sciatica C0078981 Arachnoid cysts HSDN C1963086 Confusion adverse event C1563215 Powassan encephalitis virus infection MalaCards C0015230 Exanthem C0494043 Streptobacillosis MalaCards C0427068 Legs weakness C1850808 Miyoshi myopathy MalaCards|HPO C0349588 Stature short C1853623 Fryns-aftimos syndrome MalaCards C0002962 Angina C0001726 Affective symptoms HSDN C0027796 Neuralgias C0013295 Duodenal ulcer HSDN C0012569 Double vision C0003534 Aphakia HSDN C0018524 Hallucinate C0022758 Kap HSDN C0009676 Confusion state C0027663 Neoplasms, multiple primary HSDN C0270948 Neurogenic muscular atrophy C0342281 Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus MalaCards C0178417 Anhedonia C0038551 Stimulation, subliminal HSDN C0917816 Deficiency mental C1855255 Pseudoarylsulfatase a deficiency MalaCards|HPO C1963137 Hydrocephalus adverse event C0085132 Mucopolysaccharidosis vii HPO C0231791 In toe C0220668 Congenital contractural arachnodactyly HPO C0497406 Over weight C4050613 Anxiety scale (basc-2) HSDN C0344306 Intercostal neuralgia C4075694 Intercostal neuralgia as late effect of trauma UMLS C0004134 Dyssynergia C0005967 Bone neoplasms HSDN C4085210 Usual severity pain C0003646 Aptitude HSDN C0027497 Queasy C0206715 Neoplasms, neuroepithelial HSDN C2024893 Cardiovascular surgery result: fatigue C0919267 Ovarian neoplasm HSDN C4084788 Have dizziness C0031212 Personality disorders HSDN C0013604 Edematous C0007117 Basal cell carcinoma HSDN C0000737 Abdomen pain C1962986 Glaucoma adverse event HSDN C0013404 Respiratory difficulty C1319688 Blister dose form HSDN C0917801 Sleep disorder insomnia C0860649 Insomnia due to organic factor UMLS C0036572 Convulsion C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards|UMLS C1279888 Proteinuria of undiagnosed cause C0220847 C hepatitis virus HSDN C0009676 Confusion state C0004153 Atherosclerosis HSDN C3887873 Hearing loss C0037315 Sleep apnea syndromes HSDN C4085211 Pain distress question C0001125 Acidosis, lactic HSDN C0018681 Headache, cephalalgia C1541316 Adult giant cell glioblastoma UMLS C4085210 Usual severity pain C0009443 Common cold HSDN C0040822 D tremors C0012979 Canine disease HSDN C0700078 Deep tendon reflex decrease C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2711266 Infection by anisakis larva MalaCards C4085317 Diarrhea frequency C0342731 Deficiency of mevalonate kinase MalaCards C3641756 Have diarrhea C0039240 Supraventricular tachycardia HSDN C0018772 Deafness C0015457 Expression facial HSDN C0040034 Thrombocytopenia C3160739 Fanconi anemia, complementation group e MalaCards|HPO C0518090 Frequency of pain question C0029877 Ear inflammation HSDN C1963067 Atrial fibrillation adverse event C1970119 Cardiac arrhythmia, ankyrin-b-related MalaCards|HPO C0000737 Abdomen pain C1333951 Helicobacter pylori-related gastric adenocarcinoma UMLS C1565249 Limitation, mobility C0686353 Muscular dystrophies, limb-girdle HSDN C0271215 Blindness legal C1274789 Ligneous conjunctivitis MalaCards|HPO C0349588 Stature short C0751918 Cockayne pelizaeus merzbacher disease MalaCards C4084802 Usual severity diarrhea C3888013 Hypnoses HSDN C4084768 Usual severity vomiting C0018805 Heart injuries HSDN C0013404 Respiratory difficulty C0085129 Bronchial hyperreactivity MalaCards C0024031 Back pain lower back C0013990 Pathological accumulation of air in tissues HSDN C4084776 Weight loss C0153415 Malignant neoplasm of lower third of esophagus MalaCards C3829611 Nausea frequency C0005940 Bone diseases HSDN C0863106 Afebrile convulsion C4015395 Generalized epilepsy with febrile seizures plus, type 9 MalaCards C4085862 Bothered by nausea C0030330 Panniculitis, peritoneal HSDN C4084802 Usual severity diarrhea C0015656 Fasciolopsiasis DiseaseOntology C0013428 Painful urination C1335926 Schistosoma hematobium-related bladder squamous cell carcinoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0018805 Heart injuries HSDN C4085862 Bothered by nausea C0002989 Epithelioid hemangioma of skin HSDN C0030193 Sense of pain C0221290 Chondromyxoid fibroma UMLS C0012833 Dizzy C0035243 Respiratory tract infections HSDN C0232493 Epigastric pain C3178970 Entrapment, pudendal nerve MalaCards C3539889 Pelvic pain increasing in severity C0015558 Fallopian tube neoplasms HSDN C0424755 Fever symptoms C0020522 Delayed hypersensitivity HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013377 Dysgerminoma HSDN C1962972 Proteinuria adverse event C0024668 Mammary neoplasms, experimental HSDN C0012833 Dizzy C0997768 Glaucoma HSDN C0035078 Failure kidney C0019250 Hereditary factor i deficiency disease MalaCards C4084788 Have dizziness C0302148 Blood clot HSDN C4085317 Diarrhea frequency C0009021 Clonorchiasis DiseaseOntology C0019209 Large liver C0039292 Tangier disease MalaCards|HPO C2032395 Pelvic pain on the left C0236969 Substance-related disorders HSDN C4084784 Diarrhea C0025063 Mediastinal neoplasms HSDN C1962972 Proteinuria adverse event C0000833 Abscess HSDN C1963090 Dehydration adverse event C0268080 Hypercalcemia, idiopathic, of infancy HPO C2024893 Cardiovascular surgery result: fatigue C3542413 Cdisc adas-cog - comprehension HSDN C0040264 Ear ringing sound C0013990 Pathological accumulation of air in tissues HSDN C0020578 Hyperventilate C0021400 Influenza HSDN C2024878 Cardiovascular surgery result: dyspnea C0854795 Resectable hepatic malignant neoplasm MalaCards C0035078 Failure kidney C2609260 Caudal dysplasia syndrome HPO C0917816 Deficiency mental C0023014 Language development disorders MalaCards C0036572 Convulsion C1328349 Neuropathy ataxia and retinis pigmentosa MalaCards|HPO|UMLS C0000737 Abdomen pain C1710111 Small intestinal squamous cell carcinoma UMLS C4042891 Sleep wake disorders C0085096 Peripheral vascular diseases HSDN C0030193 Sense of pain C0949691 Spondylarthropathies HSDN C4084788 Have dizziness C0029443 Osteomyelitis HSDN C0242936 Center pain C0162566 Porphyria cutanea tarda HSDN C2984058 Have pain C0009241 Cognition disorders HSDN C0857305 Thrombocytopenia purpura C0011581 Depressive disorder HSDN C2203646 Jaundice C0267878 Mirizzi syndrome HSDN C0013132 Drooling C1859711 Arthrogryposis multiplex congenita with whistling face MalaCards C1565249 Limitation, mobility C3850152 Navigation, spatial HSDN C2984058 Have pain C0017572 Gingival recession HSDN C0042798 Vision dim C1859069 Brittle bone disorder OrphaNet C1999266 Depression adverse event C0035372 Rett syndrome OrphaNet|HPO|MalaCards C0002962 Angina C0997768 Glaucoma HSDN C0015230 Exanthem C0343553 Smallpox without rash UMLS C3898969 Have been vomiting C4085635 Appetite quality question HSDN C0018772 Deafness C0019163 Hepatitis b HSDN C0086769 Panic attack C1302282 Chromaffin cell neoplasm MalaCards C0003862 Pain joint C3898105 Oligoarticular juvenile idiopathic arthritis MalaCards C4084784 Diarrhea C2984572 Malaria pathway HSDN C1963137 Hydrocephalus adverse event C3711162 Metatropic dysplasia type 1 MalaCards C4085211 Pain distress question C0016724 Froehlich's syndrome HSDN C2911645 Weight loss adverse event C0036457 Scrapie HSDN C0007166 Cardiac output decreased C1548578 Location characteristic id - smoking HSDN C1549543 Administration method - pain C0282507 Heat stress disorders HSDN C1384666 Decreased hearing C3813607 Infantile gastroesophageal reflux HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0236792 Asperger syndrome HSDN C1557397 Adverse event associated with pain C0085092 Parenting behavior HSDN C4085210 Usual severity pain C0039747 Thecoma HSDN C0746674 Muscle weakness generalized C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C0013362 Dysarthrias C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C0151786 Weakness muscle C0029089 Ophthalmoplegia MalaCards C0024031 Back pain lower back C0236969 Substance-related disorders HSDN C0037384 Snore C0019829 Hodgkin disease HSDN C3887638 Failure to thrive in infant C4014258 Immunodeficiency, common variable, 11 MalaCards C0559753 Daytime enuresis C0270328 Diurnal enuresis UMLS C2169806 Tic C0019693 Hiv infections HSDN C2984058 Have pain C0018467 Habituation, psychophysiologic HSDN C0042963 Symptoms vomiting C0024776 Maple syrup urine disease HPO|UMLS C1000483 Genus anemia C1836327 Rhabdoid tumor predisposition syndrome 1 (disorder) MalaCards C4085222 Nausea C0344434 Atrial fibrillation ecg HSDN C3146279 Coma C1963274 Vasculitis adverse event HSDN C0086437 Joint hypermobility C0346104 Follicular atrophoderma and basal cell epitheliomata MalaCards C0240715 Perineal lump C2584928 Mature cystic teratoma of testicle UMLS C0518090 Frequency of pain question C0023827 Liposarcoma HSDN C0019209 Large liver C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards|HPO C0026838 Spasticity muscle C0018564 Hand deformities HSDN C0000737 Abdomen pain C0004096 Asthma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C1522137 Hypertriglyceridemia result HSDN C3146279 Coma C0036357 Psychology, schizophrenic HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0021799 Interprofessional relations HSDN C0018991 Paralysis one side of body C1290877 Extremities disorders UMLS C4085661 Usual severity nausea C1855652 Fetus small for gestational age HSDN C0278134 Anesthesias C0521484 Anaesthesia of mucous membrane UMLS C0270948 Neurogenic muscular atrophy C1855606 Burton syndrome MalaCards C0026821 Cramp C1384672 Hpt gene HSDN C0018784 Deafness sensorineural C2931760 Acrocallosal syndrome, schinzel type MalaCards|HPO C3829611 Nausea frequency C2936636 Anticipation, psychological HSDN C0030193 Sense of pain C0206654 Leiomyomatosis HSDN C2919142 Short stature adverse event C0599973 Waardenburg anophthalmia syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0015458 Facial hemiatrophy HSDN C0043068 Friderichsen-waterhouse syndrome C0302148 Blood clot HSDN C0522224 Palsied C0748830 Skull fracture basilar HSDN C0522224 Palsied C0035369 Retroviridae infections HSDN C0085632 Listlessness C0795833 Kleefstra syndrome HPO C0022346 Yellow skin C0241910 Hepatitis, autoimmune UMLS C0013604 Edematous C0012817 Diverticulum HSDN C1549543 Administration method - pain C0023374 Lesch-nyhan syndrome HSDN C4084774 Have weight loss C4041080 Neurocognitive disorders HSDN C4085661 Usual severity nausea C0428953 Ecg infarction myocardial HSDN C0030200 Intractable pain C0009088 Cluster headache HSDN C0232199 Embryocardia C0264886 Conduction disorder of the heart UMLS C4085210 Usual severity pain C0036285 Scarlet fever HSDN C0424755 Fever symptoms C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C3641756 Have diarrhea C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C0029163 Hemorrhage mouth C0031345 Pharyngeal diseases HSDN C0033377 Caudal displacement C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO C0020578 Hyperventilate C0079744 Diffuse large b-cell lymphoma HSDN C0008031 Pain chest C1527336 Sjogren's syndrome HSDN C1963091 Diarrhea adverse event C0019911 Hookworm infections HSDN C0013404 Respiratory difficulty C1516552 Chronic idiopathic myelofibrosis, fibrotic stage UMLS C1263846 Attention deficit disorder with hyperactivity C3280355 Chromosome 15q25 deletion syndrome MalaCards C0344315 Mood depressed C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0023015 Language handicap C0015397 Disorder of eye HSDN C0030193 Sense of pain C0034091 Pulmonary veno-occlusive disease (disorder) HSDN C0020672 Body temperature decreased C0014118 Endocarditis HSDN C0020455 Hypergammaglobulinemia C0041327 Tuberculosis, pulmonary HSDN C4084802 Usual severity diarrhea C0037322 Active eye movement sleep HSDN C0206160 Retic count elevated C3150343 Hemolytic anemia, nonspherocytic, due to hexokinase deficiency HPO C4084788 Have dizziness C1963138 Hypertension adverse event HSDN C0587246 Extremity weakness C1834339 Myopathy, actin, congenital, with excess of thin myofilaments HPO C0042798 Vision dim C0034960 Refsum disease OrphaNet|HPO C4084768 Usual severity vomiting C2748608 Lead poisoning, susceptibility to HPO C0424755 Fever symptoms C0023487 Acute promyelocytic leukemia HSDN C0424755 Fever symptoms C0039685 Tetralogy of fallot HSDN C0011206 Delirium acute C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C4085211 Pain distress question C0005690 Bladder fistula HSDN C1963091 Diarrhea adverse event C1846172 Hydranencephaly and abnormal genitalia HPO C0013604 Edematous C2936917 Infantile polyarteritis MalaCards C0424755 Fever symptoms C0012979 Canine disease HSDN C0013404 Respiratory difficulty C0085073 Prosthesis-related infection HSDN C0005745 Blepharoptosis C3281235 Baraitser-winter syndrome 2 MalaCards C0010520 Skin cyanosis C1962963 Osteoporosis adverse event HSDN C0241210 Speaking delay C0221060 Mobius syndrome MalaCards C0034933 Abnormal reflexes C0011853 Diabetes mellitus, experimental HSDN C0030193 Sense of pain C0014059 Encephalomyelitis, acute disseminated HSDN C0398650 Idiopathic thrombocytopenia purpura C0460137 Push down or depress HSDN C2911647 Weight gain adverse event C0043167 Pertussis HSDN C1963091 Diarrhea adverse event C0001580 Adolescent behavior HSDN C0522224 Palsied C3827868 Tachycardia by ecg finding HSDN C1963087 Constipation adverse event C0005940 Bone diseases HSDN C0700590 Diaphoresis excessive C1302282 Chromaffin cell neoplasm MalaCards C2984058 Have pain C0010246 Coxsackievirus infections HSDN C0042963 Symptoms vomiting C0014761 Erythroblastosis, fetal HSDN C0021359 Infertility C0268060 Juvenile hemochromatosis MalaCards C0026826 High muscle tone C0022716 Menkes kinky hair syndrome OrphaNet|HPO|MalaCards C1510417 Apraxia of gait C0026650 Movement disorders HSDN C0030552 Paralysis partial C0009375 Colonic neoplasms HSDN C3665492 Pigmentations C0004767 Bartholin cyst MalaCards C0270948 Neurogenic muscular atrophy C0410226 Congenital myotonic dystrophy MalaCards C4084766 Vomiting C0003047 Animal disease HSDN C0002962 Angina C0020635 Hypopituitarism HSDN C0149777 Skin abscess C4014954 Neutropenia, severe congenital, 6, autosomal recessive MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0003614 Appendiceal neoplasms HSDN C0030193 Sense of pain C0027726 Nephrotic syndrome HSDN C1549543 Administration method - pain C0004239 Atrial flutter HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018946 Hematoma, subdural HSDN C2237041 Shox gene with short stature C2930978 Richieri costa da silva syndrome MalaCards C0030193 Sense of pain C1175175 Severe acute respiratory syndrome HSDN C0270948 Neurogenic muscular atrophy C2750786 Muscular dystrophy, congenital, due to integrin alpha-7 deficiency HPO C1557397 Adverse event associated with pain C0836924 Thrombocytosis HSDN C0033377 Caudal displacement C1846128 Ptosis, hereditary congenital 2 MalaCards C0010520 Skin cyanosis C0151744 Myocardial ischemia HSDN C4085222 Nausea C0023283 Leishmaniasis, cutaneous HSDN C2036502 Stuttering first noticed by person C0038506 Stuttering UMLS C1384666 Decreased hearing C0008370 Cholestasis HSDN C0002622 Amnesias C0035243 Respiratory tract infections HSDN C0151889 Reflexes tendon increased C0040156 Thyrotoxicosis MalaCards C0020578 Hyperventilate C0038436 Post-traumatic stress disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1963059 Adrenal insufficiency adverse event HSDN C2984058 Have pain C0334531 Mesonephric tumor HSDN C0038002 Spleen enlargement C0342907 Sitosterolemia MalaCards|HPO C0019209 Large liver C0856761 Budd-chiari syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0035801 Diseases rodent HSDN C0454644 Delayed language development C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C3274924 Have been coughing C0549472 Pneumonia, cholesterol MalaCards C1963252 Tremor adverse event C0042769 Virus diseases HSDN C0241157 Skin pustule C0086922 Purpura rheumatoid OrphaNet|MalaCards C4085548 Usual severity dizziness C0001721 Emotional affect HSDN C0426579 Anorexia symptom C0038160 Staphylococcal infections HSDN C4084784 Diarrhea C0020502 Hyperparathyroidism HSDN C3898969 Have been vomiting C0027873 Neuromyelitis optica HSDN C2984058 Have pain C0085298 Sudden cardiac death HSDN C0011206 Delirium acute C0003467 Anxiety HSDN C0030552 Paralysis partial C0162871 Aortic aneurysm, abdominal HSDN C3641756 Have diarrhea C1704421 Skin pigmentation disorder HSDN C1950154 Insomnia homeopathic medication C3178970 Entrapment, pudendal nerve MalaCards C0030193 Sense of pain C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0007758 Cerebellar ataxia C0020179 Huntington disease HSDN C0009806 Constipate C0024299 Lymphoma HSDN C0042571 Vertigo subjective C1836544 Schindler disease, type i OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0339534 Usher syndrome type 2 OrphaNet|HPO|MalaCards C0542476 Forgetful C1112155 Hereditary non-polyposis colorectal cancer syndrome HPO C0234144 Dysgraphia C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0242936 Center pain C0022364 Jaw neoplasms HSDN C0042755 Virilisation C0017075 Ganglioneuroma HSDN C2187990 Unable to perform sex C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0000737 Abdomen pain C1962963 Osteoporosis adverse event HSDN C0221752 Rbc urine C2931916 Midline granulomatosis MalaCards C1000483 Genus anemia C1855868 Polyglandular deficiency syndrome, persian-jewish type HPO C0019572 Hairiness C0796232 Bohring syndrome MalaCards|HPO C0042571 Vertigo subjective C0042029 Urinary tract infection HSDN C2237041 Shox gene with short stature C4015242 Retinal dystrophy, juvenile cataracts, and short stature syndrome MalaCards C0851578 Disorder sleep C0042035 Urination disorders HSDN C0231785 Spasm carpopedal C3715128 Hypocalcemia, autosomal dominant 1 UMLS C0026838 Spasticity muscle C1858114 Huntington disease-like 3 (disorder) MalaCards|UMLS C4084776 Weight loss C0020179 Huntington disease HSDN C0030486 Extremity paralysis, lower C3539923 Cdisc adas-cog - orientation summary score HSDN C0019572 Hairiness C1841972 Glucocorticoid receptor deficiency OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0016658 Fracture bone HSDN C0040259 Tinea pedis C0347555 Friction blister HSDN C0024031 Back pain lower back C1561518 Pleasure - animals raised for recreation HSDN C0018777 Deafness, conductive C0017653 Glomus tumor HSDN C0030193 Sense of pain C0024694 Mandibular neoplasms HSDN C0015469 Facial paralysis C0003873 Rheumatoid arthritis HSDN C0040822 D tremors C0243026 Sepsis HSDN C0018681 Headache, cephalalgia C0009400 Colorado tick fever DiseaseOntology|MalaCards C1963249 Tinnitus adverse event C0079487 Helicobacter infections HSDN C0973461 Dysphasia C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C1565249 Limitation, mobility C0010709 Cyst HSDN C0002622 Amnesias C0752155 Central nervous system vascular malformations HSDN C1963091 Diarrhea adverse event C0024117 Chronic obstructive airway disease HSDN C4084767 Bothered by vomiting C0043246 Laceration HSDN C4084776 Weight loss C0018809 Heart neoplasm HSDN C0015230 Exanthem C0477485 Other psoriasis UMLS C4084726 Distress cough C0035435 Rheumatism HSDN C4085317 Diarrhea frequency C0041948 Uremia HSDN C3887873 Hearing loss C0021051 Immunologic deficiency syndromes HSDN C0034155 Thrombotic thrombocytopenic purpura C0009319 Colitis HSDN C0020672 Body temperature decreased C0848377 Trauma to the abdomen HSDN C0009806 Constipate C0001624 Adrenal gland neoplasms HSDN C4084784 Diarrhea C0004239 Atrial flutter HSDN C0022107 Fussiness C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0857305 Thrombocytopenia purpura C2718087 Vitamin k deficiency bleeding HSDN C0027796 Neuralgias C0035242 Respiratory tract diseases HSDN C4084723 Constipation C0018799 Heart diseases HSDN C0042963 Symptoms vomiting C0012746 Dissociative disorder HSDN C0004604 Pain back C0025063 Mediastinal neoplasms HSDN C0151889 Reflexes tendon increased C1968845 Primary lateral sclerosis, adult, 1 MalaCards C3641756 Have diarrhea C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0039070 Collapse fleeting C0017601 Glaucomas HSDN C3496180 Sleep apnea C0410529 Hypochondroplasia (disorder) MalaCards|HPO C0018524 Hallucinate C0338430 Limbic encephalitis HSDN C0917801 Sleep disorder insomnia C0917799 Hypersomnia UMLS C0454644 Delayed language development C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C0026826 High muscle tone C0265425 9p partial monosomy syndrome OrphaNet|MalaCards C3665492 Pigmentations C0153460 Malignant neoplasm of tail of pancreas MalaCards C0018524 Hallucinate C0023434 Chronic lymphocytic leukemia HSDN C0018772 Deafness C1839566 Charcot-marie-tooth disease, x-linked recessive, 5 OrphaNet|HPO|MalaCards C0020455 Hypergammaglobulinemia C0042161 Uveal diseases HSDN C3146279 Coma C0023891 Liver cirrhosis, alcoholic HSDN C0030794 Pelvis pain C0019693 Hiv infections HSDN C4084724 Usual severity constipation C0025500 Mesothelioma HSDN C0019209 Large liver C0272258 Cryoglobulinemia, primary MalaCards C0162835 Hypopigmentation C0268494 Oculocutaneous albinism type 1 MalaCards C0020458 Hyperhydrosis C1849322 Sandhoff disease, infantile type HPO C4084767 Bothered by vomiting C0949570 Allergies wheat HSDN C1557397 Adverse event associated with pain C0018418 Gynecomastia HSDN C0040460 Dental pain C0009088 Cluster headache HSDN C3887873 Hearing loss C0038525 Subarachnoid hemorrhage HSDN C3463815 Feel fatigue C0029463 Osteosarcoma HSDN C4085317 Diarrhea frequency C0031154 Peritonitis HSDN C2036535 Stuttering improved by getting on stage C0038506 Stuttering UMLS C0036572 Convulsion C0024143 Lupus nephritis MalaCards|HSDN C1963091 Diarrhea adverse event C0020522 Delayed hypersensitivity HSDN C2315100 Pediatric failure to thrive C0162651 Gastric outlet obstruction HSDN C2362324 Pediatric obesity C0085207 Gestational diabetes HSDN C0851578 Disorder sleep C0032787 Postoperative complications HSDN C1384666 Decreased hearing C1853566 Genitopatellar syndrome MalaCards|HPO C0036572 Convulsion C1321575 Rolandic march UMLS C2984058 Have pain C0030318 Panic state HSDN C2911647 Weight gain adverse event C0007785 Cerebral infarction HSDN C3887638 Failure to thrive in infant C0431375 Classical lissencephaly MalaCards C0042420 Vasovagal episode C0085380 Anxiety dental HSDN C0011991 Loose stools C0008066 Child behavior disorders HSDN C3463815 Feel fatigue C0152264 Familial erythrocytosis OrphaNet|HPO C0023015 Language handicap C0015923 Fetal alcohol syndrome HSDN C0035229 Respiratory function impaired C1836602 Bruck syndrome 2 OrphaNet|HPO|MalaCards C1959630 Eye pain adverse event C0011884 Diabetic retinopathy HSDN C0004134 Dyssynergia C0014544 Epilepsy UMLS C0018681 Headache, cephalalgia C0039981 Thoracic neoplasms HSDN C0039870 Leanness C0039336 Gustatory sense HSDN C0030552 Paralysis partial C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C0151889 Reflexes tendon increased C1846367 Spinocerebellar ataxia 19 HPO C4084802 Usual severity diarrhea C0035066 Renal artery obstruction HSDN C2919142 Short stature adverse event C0016788 Fucosidase deficiency disease MalaCards|HPO C0004134 Dyssynergia C1848200 Subcortical band heterotopia, x-linked HPO C0700078 Deep tendon reflex decrease C1849386 Myoglobinuria, acute recurrent, autosomal recessive MalaCards|HPO C1565249 Limitation, mobility C0002694 Amputation traumatic HSDN C0349588 Stature short C3150653 Fanconi anemia, complementation group o MalaCards|HPO C3146279 Coma C0019557 Hip fx HSDN C2096293 Ent surgical result ear vertigo C0677866 Brain stem neoplasms HSDN C0518090 Frequency of pain question C0027721 Lipoid nephrosis HSDN C0270795 Monopareses C4049386 Spastic monoparesis UMLS C0030486 Extremity paralysis, lower C0085073 Prosthesis-related infection HSDN C0015799 Feminisation C0010417 Cryptorchidism HSDN C0206160 Retic count elevated C2749759 Macrothrombocytopenia-stomatocytosis, mediterranean HPO C0018681 Headache, cephalalgia C1377917 Stage i nasopharyngeal carcinoma UMLS C4085661 Usual severity nausea C0302148 Blood clot HSDN C1963086 Confusion adverse event C0032916 Mahaim type pre excitation HSDN C2984058 Have pain C0242350 Erectile dysfunction HSDN C2096293 Ent surgical result ear vertigo C0042029 Urinary tract infection HSDN C0029163 Hemorrhage mouth C0015519 Factor x deficiency HSDN C1557397 Adverse event associated with pain C0002448 Ameloblastoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010267 Cranial nerve neoplasms HSDN C1963184 Nystagmus adverse event C2677500 Oculoauricular syndrome MalaCards|HPO C0015468 Face pain C0152054 Therapeutic touch HSDN C1961131 Cough adverse event C0007137 Squamous cell carcinoma HSDN C3146279 Coma C0342273 Transient neonatal diabetes mellitus MalaCards C1963281 Vomiting adverse event C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C0015672 Decreased energy C0020179 Huntington disease HSDN C0030554 Abnormal sensation C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0040822 D tremors C1000483 Genus anemia HSDN C1963065 Apnea adverse event C1306577 Dies patient HSDN C0522224 Palsied C0022661 Kidney failure, chronic HSDN C3641755 Have constipation C0032927 Precancerous conditions HSDN C3539896 Pelvic pain occurs with urination C0037369 Smoking HSDN C3163620 Hypotension adverse event C0376300 Dengue shock syndrome MalaCards C2984058 Have pain C0024638 Class ii division 2 malocclusion HSDN C4085211 Pain distress question C0237104 Spirituality HSDN C4084724 Usual severity constipation C0002792 Anaphylaxis HSDN C4085317 Diarrhea frequency C0086647 Mucopolysaccharidosis type iiia HPO C1557397 Adverse event associated with pain C0014869 Peptic esophagitis HSDN C3541349 Syncope C0022744 Knee injury HSDN C0008031 Pain chest C0021400 Influenza HSDN C0036572 Convulsion C3539123 Ceroid lipofuscinosis, neuronal, 11 MalaCards|UMLS C0040485 Wryneck C0393735 Headache disorders HSDN C4085211 Pain distress question C0038531 Subclavian artery stenosis HSDN C2911645 Weight loss adverse event C0007787 Transient ischemic attack HSDN C0349588 Stature short C1859519 Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification MalaCards C4084784 Diarrhea C0002063 Alkalosis HSDN C4084726 Distress cough C0206138 Crest syndrome MalaCards C0009806 Constipate C0042812 Acuity visual HSDN C0031911 Pigment deposition C0205824 Liposarcoma, dedifferentiated MalaCards C1961131 Cough adverse event C0262655 Recurrent urinary tract infection HSDN C0018772 Deafness C3277723 Joubert syndrome 12 MalaCards C4084767 Bothered by vomiting C0041952 Uerterolithiasis HSDN C4084769 Vomiting frequency C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C0917816 Deficiency mental C2931426 Orofaciodigital syndrome type1 OrphaNet|HPO C3815497 Cough C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive OrphaNet|MalaCards C2203646 Jaundice C3665349 Secondary hypothyroidism OrphaNet|MalaCards C0004134 Dyssynergia C0026764 Multiple myeloma HSDN C4084766 Vomiting C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C0020450 Hyperemesis gravidarum C0032963 Pregnancy complications, cardiovascular HSDN C1963184 Nystagmus adverse event C1866504 Photosensitive trichothiodystrophy MalaCards C1963170 Hypothermia adverse event C0025202 Melanoma HSDN C0023380 Lethargy C0011268 Senile dementia UMLS C0878773 Bladder hyperactive C0007786 Brain ischemia HSDN C0587246 Extremity weakness C3501891 Mitochondrial dna depletion myopathy, autosomal recessive MalaCards C0023012 Delay language C4015558 Temple syndrome MalaCards C3539895 Pelvic pain occurs with bowel movement C0085222 Psoas muscle abscess HSDN C2984058 Have pain C2186740 Reported urticaria HSDN C0023014 Developmental disorder language C0039474 Temperament HSDN C3665492 Pigmentations C0043346 Xeroderma pigmentosum MalaCards C0023014 Developmental disorder language C4049644 Depression HSDN C0085636 Light sensitivity C0017609 Glaucoma, neovascular OrphaNet|MalaCards C0036572 Convulsion C0574085 3-methylglutaconic aciduria type 4 OrphaNet|MalaCards C3641756 Have diarrhea C0268322 Chester-type porphyria HPO C0012833 Dizzy C0012644 Animal disease models HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0001430 Adenoma HSDN C0033774 Skin pruritus C2980106 Prurigo, mitis UMLS C0151825 Ostalgia C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C0476273 Distress respiratory C0796274 Brown-vialetto-van laere syndrome MalaCards C0004134 Dyssynergia C0265201 De sanctis-cacchione syndrome MalaCards|HPO C0233565 Bradykinesia C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C4084774 Have weight loss C0037417 Identification, social HSDN C1963274 Vasculitis adverse event C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C2242996 Tingling C3714514 Infection HSDN C0019214 Hepatosplenomegaly C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C3887873 Hearing loss C0042769 Virus diseases HSDN C0085650 Purpura fulminans C0023219 Leg dermatoses HSDN C0002170 Alopecia disorders C2931808 Chromosome 13 ring MalaCards C0030486 Extremity paralysis, lower C0022650 Kidney calculi HSDN C3274924 Have been coughing C1565106 Headache disorders, primary HSDN C4085661 Usual severity nausea C0022650 Kidney calculi HSDN C0003126 Smell loss C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C3887638 Failure to thrive in infant C1857555 Hsd11b2, arg337cys HPO C0232462 Appetite decrease C2931842 Diaphyseal dysplasia 1, progressive MalaCards|HPO C4084773 Bothered by weight gain C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C3887638 Failure to thrive in infant C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C4084723 Constipation C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C1849158 Insulin-like growth factor i, resistance to, due to increased binding protein HPO C2984058 Have pain C0023892 Biliary cirrhosis HSDN C0018784 Deafness sensorineural C3889636 Spinocerebellar ataxia 37 MalaCards C1856661 Cornea cloudy C0086652 Mucopolysaccharidosis type ivb HPO C1963063 Anorexia adverse event C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0241210 Speaking delay C2748572 Sesame syndrome HPO C4084773 Bothered by weight gain C2004491 Cicatrix HSDN C1260880 Nasal drip C1336256 Stage iii carcinoma of nasal cavity UMLS C2032395 Pelvic pain on the left C0042063 Urogenital abnormalities HSDN C1971624 Appetite absent C1721053 Female athlete triad HSDN C0018772 Deafness C0036864 Sexual relations HSDN C0019209 Large liver C2718068 Beta-galactosidase deficiency MalaCards C0019572 Hairiness C1412749 Bbs4 gene HPO C0497406 Over weight C0032969 Pregnancy in diabetics HSDN C0030552 Paralysis partial C0037116 Silicosis HSDN C0005874 Blush C0157743 Vibratory urticaria MalaCards C0027796 Neuralgias C0033348 Language program HSDN C0018965 Blood urine C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0344232 Blurred vision C0242287 Isaacs syndrome HPO C0002624 Amnesia retrograde C0002395 Alzheimer's disease HSDN C3539896 Pelvic pain occurs with urination C2936290 Femoracetabular impingement HSDN C2203646 Jaundice C0010481 Cushing syndrome HSDN C0009806 Constipate C1837218 Cleft palate, isolated HSDN C0030193 Sense of pain C1546949 Event consequence - death HSDN C4049602 Hyperactivity C0035934 Rubinstein-taybi syndrome HPO C2237041 Shox gene with short stature C0796016 Microphthalmia, syndromic 1 OrphaNet|HPO|MalaCards C0027424 Congestion nasal C0746757 Nasal congestion chronic UMLS C4084725 Usual severity cough C0702166 Acne HSDN C1557397 Adverse event associated with pain C0221269 Pseudolymphoma HSDN C0018681 Headache, cephalalgia C0027658 Neoplasms, germ cell and embryonal HSDN C2237041 Shox gene with short stature C1835450 Leri pleonosteosis MalaCards C0424755 Fever symptoms C0036439 Scoliosis, unspecified HSDN C0036572 Convulsion C0393671 Benign frontal childhood epilepsy UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0275148 Poisoning of animal by plant HSDN C0013608 Cardiac edema C0008728 Churg-strauss syndrome HSDN C0027796 Neuralgias C1962958 Hematoma adverse event HSDN C0015469 Facial paralysis C1833835 Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency MalaCards C0030975 Disorders perception C0009244 Behavioral cognitive therapy HSDN C0851578 Disorder sleep C0020502 Hyperparathyroidism HSDN C2984058 Have pain C0004239 Atrial flutter HSDN C4085210 Usual severity pain C0152427 Polydactyly HSDN C0037763 Spasm C0007762 Cerebellar neoplasms HSDN C0184567 Pain acute C0019310 Hernia, obturator HSDN C4085210 Usual severity pain C0020162 Humerus fracture HSDN C0029537 Other chest pain C0018799 Heart diseases UMLS C0003113 Anomia C0020936 Imitative behaviors HSDN C0038506 Stutter C0521542 Brainstem infarct HSDN C3539020 Pelvic pain decreasing in frequency C0037072 Diseases sigmoid HSDN C1549543 Administration method - pain C0031030 Periapical periodontitis HSDN C0010200 Cough symptom C1710175 Squamous cell lung carcinoma, papillary variant UMLS C0030193 Sense of pain C0004659 Bacteriuria HSDN C0023380 Lethargy C0001623 Adrenal gland hypofunction HSDN C1963281 Vomiting adverse event C0002895 Anemia, sickle cell HSDN C1999266 Depression adverse event C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C4084775 Usual severity weight loss C0085435 Arthritis, reactive MalaCards C4084725 Usual severity cough C0085092 Parenting behavior HSDN C0035229 Respiratory function impaired C2931347 Cardiac form of generalized glycogenosis MalaCards|HPO C4084773 Bothered by weight gain C0015674 Chronic fatigue syndrome HSDN C0007758 Cerebellar ataxia C0004135 Ataxia telangiectasia OrphaNet|UMLS|HPO|MalaCards C0007758 Cerebellar ataxia C0162672 Merrf syndrome OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C0007137 Squamous cell carcinoma HSDN C0241137 Skin pallor C0152164 Cyclical vomiting syndrome (disorder) MalaCards C4084784 Diarrhea C0032966 Complication, neoplastic pregnancy HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0086543 Cataract nos HSDN C1963093 Dizziness adverse event C0220654 Meningeal carcinomatosis HSDN C0020580 Decreased sensation C1963064 Anxiety adverse event HSDN C4084802 Usual severity diarrhea C0341299 Collagenous sprue HSDN C0242936 Center pain C0033324 Prognathism HSDN C0242936 Center pain C0085693 Acute appendicitis nos (disorder) MalaCards C0277959 Hair coarseness C0265480 20p partial trisomy syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C4084784 Diarrhea C0156147 Crohn's disease of large bowel MalaCards C0018772 Deafness C0031154 Peritonitis HSDN C4085549 Dizziness C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C4084773 Bothered by weight gain C0022660 Kidney failure, acute HSDN C3539896 Pelvic pain occurs with urination C0206654 Leiomyomatosis HSDN C0019572 Hairiness C0020507 Hyperplasia HSDN C4084723 Constipation C0005416 Biliary dyskinesia HSDN C1963137 Hydrocephalus adverse event C1863389 Apert-crouzon disease MalaCards|HPO C0011206 Delirium acute C4013648 Polymicrogyria, bilateral temporooccipital MalaCards C0728710 Pupil constriction observed C0206368 Exfoliation syndrome HSDN C0242936 Center pain C0079173 Craniomandibular disorders HSDN C0522224 Palsied C0262655 Recurrent urinary tract infection HSDN C4084768 Usual severity vomiting C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0231528 Muscle pain generalized C0238190 Inclusion body myositis (disorder) MalaCards C0020455 Hypergammaglobulinemia C0019195 Hepatitis, viral, human HSDN C4084775 Usual severity weight loss C1546747 Specimen source codes - polyps HSDN C0026821 Cramp C0012739 Disseminated intravascular coagulation HSDN C0030486 Extremity paralysis, lower C0030297 Pancreatic neoplasm HSDN C4084723 Constipation C0235387 Porphyria type syndrome OrphaNet C4084726 Distress cough C0036983 Septic shock HSDN C0039870 Leanness C0018889 Helminthiasis HSDN C0007758 Cerebellar ataxia C0011168 Deglutition disorders HSDN C0030193 Sense of pain C0035439 Rheumatic heart disease HSDN C0233565 Bradykinesia C0018523 Hallervorden-spatz syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0002949 Aneurysm, dissecting HSDN C0010200 Cough symptom C0007873 Uterine cervical neoplasm HSDN C2203646 Jaundice C0597109 Nurse's role HSDN C0009421 Comatose C0034069 Pulmonary fibrosis HSDN C1971624 Appetite absent C0153460 Malignant neoplasm of tail of pancreas MalaCards C3815497 Cough C0014869 Peptic esophagitis HSDN C0036572 Convulsion C2677763 Stevenson-carey syndrome UMLS C1279888 Proteinuria of undiagnosed cause C2931916 Midline granulomatosis MalaCards C0017181 Gastrointestinal bleed C0220704 Shprintzen syndrome MalaCards|HPO C0010200 Cough symptom C0027932 Neurotic disorders HSDN C0009421 Comatose C0038436 Post-traumatic stress disorder HSDN C1963091 Diarrhea adverse event C0024314 Lymphoproliferative disorders MalaCards C0575081 Abnormal gait C3539494 Spastic paraplegia 53, autosomal recessive MalaCards C2096293 Ent surgical result ear vertigo C0029888 Otitis media purulent HSDN C1838869 Proximal neurogenic muscle weakness C1833373 Inclusion body myopathy, autosomal recessive MalaCards|HPO C0424755 Fever symptoms C1319688 Blister dose form HSDN C4084788 Have dizziness C0002874 Aplastic anemia HSDN C1963086 Confusion adverse event C0014548 Epilepsy, generalized HSDN C3665347 Vision impaired C1859312 Camfak syndrome OrphaNet|HPO C4084784 Diarrhea C0038356 Stomach neoplasms HSDN C0018681 Headache, cephalalgia C1827983 Migraine variants, intractable UMLS C0009421 Comatose C0042338 Herpesvirus 3, human HSDN C0013456 Pain ear C0041834 Erythema HSDN C0030554 Abnormal sensation C0038525 Subarachnoid hemorrhage HSDN C0917816 Deficiency mental C1845539 Autism, x-linked, susceptibility to, 2 (finding) HPO C3463815 Feel fatigue C0878544 Cardiomyopathies HSDN C0751265 Learning disability C1849348 Richieri costa pereira syndrome MalaCards C0231218 Malaise generalized C2983423 Stage iii hepatocellular carcinoma UMLS C0917816 Deficiency mental C0265210 Weaver syndrome OrphaNet|HPO|MalaCards C0020672 Body temperature decreased C0021400 Influenza HSDN C0857305 Thrombocytopenia purpura C0004623 Bacterial infections HSDN C0018681 Headache, cephalalgia C0022758 Kap HSDN C0242936 Center pain C0151491 Congenital musculoskeletal anomalies HSDN C0424810 Periorbital swelling C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0018989 Paresis of one side of body C0003537 Aphasia UMLS C1963252 Tremor adverse event C0019699 Hiv seropositivity HSDN C0018681 Headache, cephalalgia C0037937 Spine injury HSDN C0234146 Absent reflex C3150897 Charcot-marie-tooth disease, recessive intermediate b HPO C2237041 Shox gene with short stature C3553517 Cornelia de lange syndrome 4 MalaCards C0000737 Abdomen pain C0020676 Hypothyroidism HSDN C1963090 Dehydration adverse event C2931187 Nephropathic cystinosis MalaCards C0240735 Personality change C0236642 Pick disease of the brain HPO|UMLS C3641756 Have diarrhea C0011615 Dermatitis, atopic HSDN C0037317 Sleep disturbance C0268281 Infantile neuronal ceroid lipofuscinosis MalaCards|HPO C4084769 Vomiting frequency C0022890 Labyrinthine disorder HSDN C4085211 Pain distress question C0007098 Walker carcinoma 256 HSDN C3539020 Pelvic pain decreasing in frequency C0453996 Tobacco smoking HSDN C4085210 Usual severity pain C0020635 Hypopituitarism HSDN C0003811 Cardiac rhythm disturbance C0948264 Neuroborreliosis MalaCards C4084723 Constipation C0268579 Propionic acidemia OrphaNet|HPO C1963091 Diarrhea adverse event C2717906 Hereditary angioedema type i HPO C0030552 Paralysis partial C0042345 Varicosity HSDN C2911647 Weight gain adverse event C0162871 Aortic aneurysm, abdominal HSDN C3827868 Tachycardia by ecg finding C1840365 King denborough syndrome HPO C0151205 Periorbital edema C0521464 Edema cutaneous UMLS C0026838 Spasticity muscle C2751842 Parkinson disease 14, autosomal recessive MalaCards|HPO|UMLS C0041105 Jaw spasm C0004669 Bacteroides infections HSDN C2032395 Pelvic pain on the left C0002871 Anemia HSDN C0018681 Headache, cephalalgia C0024117 Chronic obstructive airway disease HSDN C0018681 Headache, cephalalgia C1962979 Burn adverse event HSDN C0018772 Deafness C3850026 Auditory spatial processing HSDN C0427190 Ataxia, truncal C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO|UMLS C4085210 Usual severity pain C0950123 Inborn genetic disease HSDN C1145670 Failure respiratory C1859133 Rhizomelic chondrodysplasia punctata, type 1 HPO C4084766 Vomiting C0003864 Arthritis HSDN C4085661 Usual severity nausea C1690964 Cataract HSDN C0015672 Decreased energy C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0034150 Skin purpura C0019123 Hemothorax HSDN C0150055 Pain chronic C0022661 Kidney failure, chronic HSDN C0020450 Hyperemesis gravidarum C0000768 Congenital abnormality HSDN C0349489 Fetal hypoxia C2984299 Asthma pathway HSDN C0036396 Sciatica C1135841 Zoster sine eruptione HSDN C4084775 Usual severity weight loss C0233629 Thinking and speaking disturbances HSDN C0005745 Blepharoptosis C0155338 Total ophthalmoplegia MalaCards C4084768 Usual severity vomiting C0004275 Attitude health HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042258 Vaginal neoplasms HSDN C0007859 Pain neck C0036864 Sexual relations HSDN C0312416 Morning sickness C0043121 Wernicke encephalopathy HSDN C4084802 Usual severity diarrhea C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C0497247 Blood pressure elevation C1720859 Familial partial lipodystrophy, type 1 OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0011606 Exfoliative dermatitis HSDN C0042024 Urine incontinence C0333641 Atrophic HSDN C0002962 Angina C0221752 Rbc urine HSDN C4085548 Usual severity dizziness C2364172 Adherence to medication regime HSDN C0003469 Anxiety disorder C0751157 Fraxe syndrome MalaCards C0150055 Pain chronic C0038981 Swayback HSDN C3274924 Have been coughing C1547044 Kind of quantity - smell HSDN C4020887 Photodysphoria C1691013 Macular corneal dystrophy, type ii HPO C1999266 Depression adverse event C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C0221166 Paraparesis C0023119 Lathyrism HSDN C1963063 Anorexia adverse event C0030472 Paraneoplastic syndromes HSDN C0018784 Deafness sensorineural C3494506 Pseudohypoparathyroidism, type ia HPO C0039870 Leanness C0024115 Lung diseases HSDN C0040485 Wryneck C0338465 Sandifer syndrome UMLS C0018775 Hearing loss bilateral C0018021 Goiter HSDN C0004134 Dyssynergia C0796045 Ataxia-deafness-retardation syndrome MalaCards C0007758 Cerebellar ataxia C0011860 Diabetes mellitus, non-insulin-dependent HSDN C3541349 Syncope C0162770 Right ventricular hypertrophy HSDN C4084802 Usual severity diarrhea C0023794 Lipoidosis HSDN C4084766 Vomiting C1335398 Gastric peutz-jeghers polyp MalaCards C0011991 Loose stools C0026918 Mycobacterium infections HSDN C2315100 Pediatric failure to thrive C1857558 Hsd11b2, arg279cys HPO C0031911 Pigment deposition C1858562 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 MalaCards C0349588 Stature short C0398788 Immunodeficiency syndrome, variable MalaCards|HPO C4084774 Have weight loss C2931894 Mucolipidosis 2 MalaCards|HPO C1557397 Adverse event associated with pain C0265334 Pachyonychia congenita HSDN C2237041 Shox gene with short stature C1839729 Mental retardation, skeletal dysplasia, and abducens palsy MalaCards C2911647 Weight gain adverse event C1963090 Dehydration adverse event HSDN C0018681 Headache, cephalalgia C0030807 Pemphigus, nos HSDN C3887873 Hearing loss C0018800 Cardiomegaly HSDN C2984058 Have pain C0016719 Friedreich ataxia HSDN C4084768 Usual severity vomiting C0600260 Lung diseases, obstructive HSDN C0231218 Malaise generalized C1710014 Sarcomatoid hepatocellular carcinoma UMLS C3887873 Hearing loss C0853697 Neutrophil count decreased HSDN C2132198 Abnormal blistering of the skin C2673609 Epidermolysis bullosa inversa dystrophica OrphaNet|HPO|MalaCards C0242936 Center pain C0043325 Xanthomatosis HSDN C2919142 Short stature adverse event C3810023 Verheij syndrome MalaCards C0235153 Sensory hallucination C3554605 Mc3dn2 MalaCards C0005409 Bilharzial pigment deposition C0009450 Disease caused by microorganism UMLS C0020580 Decreased sensation C0008775 Ciguatera poisoning HSDN C0016199 Pain flank C1336878 Small cell carcinoma of ureter UMLS C4084725 Usual severity cough C0023786 Mucopolysaccharidosis i OrphaNet C4085210 Usual severity pain C0019342 Genital herpes HSDN C0271215 Blindness legal C0242852 Proliferative vitreoretinopathy MalaCards C4084766 Vomiting C0026936 Mycoplasma infections HSDN C0041657 Consciousness loss C0276226 Herpes encephalitis HSDN C0018784 Deafness sensorineural C0796147 Acrocallosal syndrome MalaCards|HPO C0041657 Consciousness loss C1263960 Diabetic coma HSDN C0020538 Hbp C0342881 Familial hypercholesterolemia - homozygous OrphaNet|HPO|MalaCards C0018926 Emesis bloody C0042487 Venous thrombosis HSDN C4084766 Vomiting C0042384 Vasculitis HSDN C0020673 Hypothermia (central) (local) C1522136 Hypernatremia result HSDN C1557397 Adverse event associated with pain C0018021 Goiter HSDN C0020538 Hbp C1841972 Glucocorticoid receptor deficiency OrphaNet|HPO C0036572 Convulsion C0037926 Compression of spinal cord HSDN C2242996 Tingling C0003708 Arachnitis OrphaNet|HSDN|MalaCards C4085211 Pain distress question C0428977 Bradycardia HSDN C0011991 Loose stools C3272484 Ampulla of vater somatostatin producing net UMLS C0000737 Abdomen pain C2931876 Hirschsprung disease 1 MalaCards C0027796 Neuralgias C0031117 Peripheral neuropathy UMLS C4084767 Bothered by vomiting C1847839 Episodic ataxia, type 3 MalaCards C0027497 Queasy C1963211 Pericarditis adverse event HSDN C0012569 Double vision C0751871 Autoimmune diseases of the nervous system HSDN C1549543 Administration method - pain C0032816 Post-concussion headache HSDN C4084766 Vomiting C1552262 Nurse practitioner - family HSDN C1961131 Cough adverse event C2931916 Midline granulomatosis MalaCards C0042571 Vertigo subjective C0014175 Endometriosis HSDN C0008031 Pain chest C0009421 Comatose UMLS C3463815 Feel fatigue C0011875 Diabetic angiopathies HSDN C1963281 Vomiting adverse event C0029944 Drug overdose HSDN C1535893 Orthostatic intolerance C0019154 Hepatic vein thrombosis HSDN C1549543 Administration method - pain C0037221 Situs inversus HSDN C3146279 Coma C0015745 Ingestive behavior HSDN C4085210 Usual severity pain C0814263 Meditation therapy HSDN C0042963 Symptoms vomiting C0022408 Arthropathy HSDN C0030552 Paralysis partial C0268345 Ehlers-danlos syndrome, arthrochalasia type OrphaNet|HPO C1384666 Decreased hearing C0086647 Mucopolysaccharidosis type iiia MalaCards|HPO C1963091 Diarrhea adverse event C0011616 Contact dermatitis HSDN C0340288 Angina stable C0027149 Myxoma HSDN C0000737 Abdomen pain C0005686 Urinary bladder diseases HSDN C1549543 Administration method - pain C0043202 Wolff-parkinson-white syndrome HSDN C0027498 Nausea vomiting C3661523 Congenital intestinal aganglionosis OrphaNet|HPO|MalaCards C3641755 Have constipation C0026857 Musculoskeletal diseases HSDN C3274924 Have been coughing C0008325 Cholecystitis HSDN C4084774 Have weight loss C0023051 Laryngeal diseases HSDN C3641756 Have diarrhea C0037926 Compression of spinal cord HSDN C1963087 Constipation adverse event C0002792 Anaphylaxis HSDN C2911645 Weight loss adverse event C0024894 Mastitis HSDN C0036659 Sensation disorder C0221759 Brachial plexus neuritis HSDN C2911645 Weight loss adverse event C0153460 Malignant neoplasm of tail of pancreas MalaCards C0000737 Abdomen pain C0035457 Rhinitis, allergic, perennial HSDN C0557874 Global developmental delay C3554449 Mental retardation, autosomal dominant 19 MalaCards C2984058 Have pain C0018051 Gonadal dysgenesis HSDN C2315100 Pediatric failure to thrive C0009375 Colonic neoplasms HSDN C0039070 Collapse fleeting C0020443 Hypercholesterolemia HSDN C4050613 Anxiety C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C2315100 Pediatric failure to thrive C1856306 Gsd iv, neuromuscular form, adult, with isolated myopathy HPO C4084802 Usual severity diarrhea C2984302 Leishmaniasis infection pathway HSDN C2315100 Pediatric failure to thrive C0079294 Epidermolysis bullosa dystrophica MalaCards C0233993 Sexuality related problems C0036903 Sexual aversion UMLS C1069915 Vertigo C0014457 Eosinophilia HSDN C0413252 Hypothermia due to exposure C0035358 Retroperitoneal neoplasm HSDN C0262384 Chest pain atypical C0017168 Gastroesophageal reflux disease UMLS C3274924 Have been coughing C0162359 Christ-siemens-touraine syndrome OrphaNet|MalaCards C4085317 Diarrhea frequency C1134719 Invasive ductal breast carcinoma HSDN C0018777 Deafness, conductive C1848392 Zunich neuroectodermal syndrome HPO C4084769 Vomiting frequency C0023283 Leishmaniasis, cutaneous HSDN C1579931 Depressed - symptom C0687720 Central diabetes insipidus OrphaNet|MalaCards C0043094 Weight gain C0206526 Tuberculosis, multidrug-resistant HSDN C1860844 Sparse, thin hair C1833538 Orofacial cleft 7 MalaCards C1961131 Cough adverse event C0006845 Candidiasis, chronic mucocutaneous MalaCards|HPO C0027497 Queasy C1135841 Zoster sine eruptione HSDN C0042963 Symptoms vomiting C0003811 Cardiac arrhythmia HSDN C1963065 Apnea adverse event C0340427 Familial dilated cardiomyopathy MalaCards C0007166 Cardiac output decreased C0031117 Peripheral neuropathy HSDN C2911647 Weight gain adverse event C0795623 Hepatitis a vaccine, inactivated HSDN C0151786 Weakness muscle C0751360 Becker generalized myotonia HPO C4084784 Diarrhea C0024117 Chronic obstructive airway disease HSDN C0041834 Erythematous condition C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C2936821 Spinal cerebrospinal fluid leak C0007766 Intracranial aneurysm HSDN C0015468 Face pain C0024638 Class ii division 2 malocclusion HSDN C3641891 Have itch C3276706 Small fiber neuropathy MalaCards C3146279 Coma C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C1527311 Brain edema HSDN C0016382 Cutaneous vascular engorgement C0003873 Rheumatoid arthritis HSDN C0009421 Comatose C0003492 Aortic coarctation HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C2350572 Illness behavior HSDN C0234146 Absent reflex C0410203 X-linked centronuclear myopathy OrphaNet|HPO C3641755 Have constipation C2936741 Syndrome xxyy OrphaNet|MalaCards C0007758 Cerebellar ataxia C0268272 Gangliosidosis, generalized gm1, type 2 MalaCards|HPO C4042891 Sleep wake disorders C0029458 Osteoporosis, postmenopausal HSDN C0018681 Headache, cephalalgia C1335448 Meningioma of posterior cranial fossa UMLS C0041657 Consciousness loss C1556682 Adverse event associated with infection HSDN C0034155 Thrombotic thrombocytopenic purpura C0018671 Head and neck neoplasms HSDN C3887873 Hearing loss C2931557 Chromosome 4 short arm deletion MalaCards C0026838 Spasticity muscle C0038160 Staphylococcal infections HSDN C0003550 Broca aphasia C0007786 Brain ischemia HSDN C0242936 Center pain C2939156 Development of sexuality HSDN C2984058 Have pain C0025517 Metabolic diseases HSDN C0041657 Consciousness loss C0032290 Aspiration pneumonia HSDN C0036572 Convulsion C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C0150055 Pain chronic C1541646 Spirituality therapy HSDN C1961131 Cough adverse event C0028242 Nocardia infections HSDN C1963086 Confusion adverse event C0029456 Osteoporosis HSDN C0030193 Sense of pain C0279567 Paget's disease of the breast with invasive ductal carcinoma UMLS C4084767 Bothered by vomiting C0040524 Septic toxemia HSDN C0242936 Center pain C0079731 B-cell lymphomas HSDN C4084724 Usual severity constipation C1578691 Congenital myxedema MalaCards C0151827 Pain eye C1955906 Lymphoma, extranodal nk-t-cell HSDN C0030193 Sense of pain C0008088 Child psychiatry HSDN C0036572 Convulsion C1864171 Peroxisome biogenesis disorder, complementation group 12 MalaCards C3829611 Nausea frequency C1623041 Breast-fed HSDN C0007758 Cerebellar ataxia C1855008 Mitochondrial complex ii deficiency MalaCards|HPO C0151786 Weakness muscle C0162871 Aortic aneurysm, abdominal HSDN C0022346 Yellow skin C1336223 Stage iiib carcinoma of liver cells UMLS C4085222 Nausea C0302148 Blood clot HSDN C0557874 Global developmental delay C0410174 Fukuyama type congenital muscular dystrophy OrphaNet|HPO|MalaCards C0042798 Vision dim C1856973 Encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration MalaCards C0242936 Center pain C0029417 Osteoblastoma HSDN C4084784 Diarrhea C0004114 Astrocytoma HSDN C0233514 Behavior abnormal C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C0018784 Deafness sensorineural C0027643 Neoplasm recurrence, local HSDN C2919142 Short stature adverse event C3279941 Stickler syndrome, type iv MalaCards C0000727 Abdomen acute C0010674 Cystic fibrosis HSDN C3541349 Syncope C0085417 Epilepsy, complex partial HSDN C0015300 Ocular proptosis C2930851 Intestinal lipophagic granulomatosis MalaCards C4085210 Usual severity pain C0524851 Neurodegenerative disorders HSDN C4085211 Pain distress question C0035328 Retinal vein occlusion HSDN C3539892 Pelvic pain in front C0041952 Uerterolithiasis HSDN C2055125 Temperature reported over 102 degrees fahrenheit C1304456 Congo hemorrhagic fever MalaCards C0522224 Palsied C0042454 Velopharyngeal insufficiency HSDN C0028738 Nystagmus C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0030552 Paralysis partial C1263846 Attention deficit hyperactivity disorder HSDN C0036572 Convulsion C1846171 Lissencephaly, x-linked, 2 OrphaNet|HPO|MalaCards C2984058 Have pain C0041333 Tuberculosis genitourinary HSDN C0016199 Pain flank C0043541 Zygomycoses HSDN C2315100 Pediatric failure to thrive C3806634 Deafness, dystonia, and cerebral hypomyelination MalaCards C0038002 Spleen enlargement C0042111 Urticaria pigmentosa MalaCards C1971624 Appetite absent C0038661 Suicide HSDN C0033377 Caudal displacement C1833104 Diabetes mellitus, permanent neonatal MalaCards|HPO C0040822 D tremors C0011265 Presenile dementia HSDN C0270948 Neurogenic muscular atrophy C1849321 Sandhoff disease, juvenile type HPO C0034124 Pupillary disorder C1321926 Injury of third cranial nerve HSDN C0018991 Paralysis one side of body C0032344 Poisoning aspects HSDN C0151740 Intracranial hypertension C0349604 Intracranial meningioma MalaCards C3887873 Hearing loss C0020517 Hypersensitivity HSDN C3494358 Characteristic, prodromal C0679005 Interpersonal skills HSDN C1963281 Vomiting adverse event C0035235 Respiratory syncytial virus infections HSDN C0041657 Consciousness loss C0024115 Lung diseases HSDN C0004604 Pain back C0149514 Bronchitis acute HSDN C3665347 Vision impaired C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0007859 Pain neck C0007856 Cervical rib syndrome HSDN C0024031 Back pain lower back C0007453 Cattle disease HSDN C2911647 Weight gain adverse event C0028432 Nose diseases HSDN C4085211 Pain distress question C0158454 Malunited fracture HSDN C0151786 Weakness muscle C0009319 Colitis HSDN C0037763 Spasm C2945560 Hemolytic HSDN C3539890 Pelvic pain causes awakening at night C0012817 Diverticulum HSDN C2984057 Have nausea C1550639 Specimen type - fistula HSDN C0030193 Sense of pain C4053713 Childhood malignant fibrous histiocytoma of bone UMLS C0232513 Premature tooth loss C1838257 Serpentine fibula polycystic kidney syndrome MalaCards C0003811 Cardiac rhythm disturbance C2750035 Emery-dreifuss muscular dystrophy 3 HPO C0013395 Indigestion C0232488 Abdominal colic HSDN C1962972 Proteinuria adverse event C0016045 Fibroma HSDN C0013421 Dystonia C0027947 Neutropenia HSDN C4084775 Usual severity weight loss C0015461 Facial neoplasms HSDN C0587047 Mass of trunk C0267492 Granuloma of intestine, nos UMLS C0018991 Paralysis one side of body C0029463 Osteosarcoma HSDN C0020450 Hyperemesis gravidarum C0020701 Somatization disorder HSDN C4084802 Usual severity diarrhea C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C0004604 Pain back C0749381 Thoracolumbar spine film UMLS C0031315 Phantom limb pain C0013806 Electroplexy shock therapy HSDN C0026821 Cramp C0009375 Colonic neoplasms HSDN C4084776 Weight loss C0008354 Cholera HSDN C0018681 Headache, cephalalgia C0007130 Mucinous adenocarcinoma HSDN C2024893 Cardiovascular surgery result: fatigue C2711227 Steatohepatitis HSDN C0034150 Skin purpura C0041331 Splenic tuberculoses HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024841 Matrimony, matrimonial HSDN C0015469 Facial paralysis C1263858 Muscular dystrophy congenital, merosin negative OrphaNet|HPO C4084767 Bothered by vomiting C0717360 Disease lyme vaccine HSDN C0013421 Dystonia C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia HPO C4084726 Distress cough C2930851 Intestinal lipophagic granulomatosis MalaCards C4084768 Usual severity vomiting C0018818 Ventricular septal defects HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2364172 Adherence to medication regime HSDN C4085642 Level of joint stiffness C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C0917816 Deficiency mental C0175704 Leopard syndrome MalaCards C0151786 Weakness muscle C1837454 Spinocerebellar ataxia 8 MalaCards C0018681 Headache, cephalalgia C1377919 Stage iv nasopharyngeal carcinoma UMLS C1557397 Adverse event associated with pain C0019655 Histoplasmosis HSDN C0424755 Fever symptoms C0018794 Heart block HSDN C4085211 Pain distress question C0853697 Neutrophil count decreased HSDN C3274924 Have been coughing C0033860 Psoriasis HSDN C0015672 Decreased energy C0024954 Maxillary neoplasms HSDN C0036572 Convulsion C3494973 Benign occipital epilepsy of childhood - late onset, non-intractable UMLS C0014591 Bleeding nose C0265321 Wyburn-mason syndrome MalaCards C4084726 Distress cough C0004031 Aspergillosis, allergic bronchopulmonary DiseaseOntology|OrphaNet|MalaCards C3815497 Cough C0022661 Kidney failure, chronic HSDN C0002962 Angina C0009374 Colonic disease, functional HSDN C3274924 Have been coughing C0021390 Inflammatory bowel diseases HSDN C0000737 Abdomen pain C3495559 Juvenile arthritis OrphaNet C1963170 Hypothermia adverse event C0342200 Endemic cretinism MalaCards C0917816 Deficiency mental C3165526 Congenital iodine deficiency syndrome MalaCards C1963170 Hypothermia adverse event C1962971 Myocarditis adverse event HSDN C3814778 Hemolytic index C0002895 Anemia, sickle cell MalaCards C2364082 Hyposmia C0030567 Parkinson disease MalaCards C0009806 Constipate C0030528 Paratyphoid fever DiseaseOntology|MalaCards C0020615 Hypoglycemia nos C0852654 21-hydroxylase deficiency MalaCards C4084767 Bothered by vomiting C0220754 Biotinidase deficiency MalaCards|HPO C0037036 Increased salivation C0086650 Mps iii d HPO C3539023 Pelvic pain increasing in frequency C0041952 Uerterolithiasis HSDN C0013421 Dystonia C0079541 Holoprosencephaly OrphaNet|MalaCards C1961131 Cough adverse event C0025061 Disease of mediastinum HSDN C4085210 Usual severity pain C0019556 Canine hip dysplasia HSDN C0557874 Global developmental delay C1863881 Radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation OrphaNet|MalaCards C2984058 Have pain C0014132 Endocrine gland neoplasms HSDN C0000737 Abdomen pain C0012979 Canine disease HSDN C0018991 Paralysis one side of body C0027439 Nasopharyngeal neoplasms HSDN C4084727 Cough frequency C0027746 Nerve degeneration HSDN C1963066 Joint pain adverse event C0019163 Hepatitis b DiseaseOntology|MalaCards C0019572 Hairiness C0038478 Struma ovarii HSDN C1384666 Decreased hearing C3150674 Chromosome 15q24 deletion syndrome MalaCards|HPO C4084725 Usual severity cough C0038463 Strongyloides infection HSDN C2024893 Cardiovascular surgery result: fatigue C0011127 Pressure ulcer HSDN C2315100 Pediatric failure to thrive C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency HPO C0036659 Sensation disorder C0006663 Calcinosis HSDN C0700078 Deep tendon reflex decrease C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards C2242996 Tingling C0002726 Amyloidosis HSDN C0013595 Eczematous dermatitis C0343110 Epidermolytic palmoplantar keratoderma of vorner OrphaNet|HPO C0751837 Gait ataxic C1335732 Region 17p13 allelic loss associated medulloblastoma UMLS C0032227 Effusion pleural C1384600 Systemic onset juvenile chronic arthritis MalaCards|HPO C0018772 Deafness C0040715 Chromosomal translocation HSDN C2024878 Cardiovascular surgery result: dyspnea C0016171 Fistula of intestine, excluding rectum and anus HSDN C4085661 Usual severity nausea C0002351 Altitude sickness HSDN C1963164 Lymphopenia adverse event C1969799 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation MalaCards C1557397 Adverse event associated with pain C0022572 Keratoacanthoma HSDN C0151686 Growth retardation C2931374 Al awadi teebi farag syndrome OrphaNet C0042024 Urine incontinence C0023895 Liver diseases HSDN C4085210 Usual severity pain C0233629 Thinking and speaking disturbances HSDN C1962972 Proteinuria adverse event C0342443 Adrenal cushing's syndrome HSDN C4085222 Nausea C0011875 Diabetic angiopathies HSDN C0020578 Hyperventilate C2984572 Malaria pathway HSDN C1557397 Adverse event associated with pain C0024205 Lymphadenitis HSDN C0013362 Dysarthrias C0035410 Rhabdomyolysis MalaCards C0042963 Symptoms vomiting C0017612 Glaucoma, open-angle HSDN C1963086 Confusion adverse event C0028242 Nocardia infections HSDN C0041834 Erythematous condition C0021100 Bullous impetigo OrphaNet|MalaCards C0497247 Blood pressure elevation C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C0349588 Stature short C3279792 Short-rib thoracic dysplasia 7 with or without polydactyly MalaCards C0917816 Deficiency mental C3150998 Spinocerebellar ataxia, autosomal recessive 10 MalaCards|HPO C0027066 Myoclonic jerking C0393624 Palatal-tympanic myoclonus UMLS C0150055 Pain chronic C0038160 Staphylococcal infections HSDN C0398650 Idiopathic thrombocytopenia purpura C0020456 Hyperglycemia HSDN C0003467 Angst C0022134 Islet cell adenoma MalaCards C0011168 Disorder deglutition C0040100 Thymoma OrphaNet|MalaCards C0002170 Alopecia disorders C0023645 Lichen planus follicularis OrphaNet|MalaCards C3641756 Have diarrhea C0019202 Hepatolenticular degeneration HSDN C3887873 Hearing loss C2675512 Diamond-blackfan anemia 7 MalaCards C0043094 Weight gain C0004364 Autoimmune diseases HSDN C0036572 Convulsion C0422855 Epileptic vertigo UMLS C0085636 Light sensitivity C0549567 Pigmentation disorders HSDN C4042891 Sleep wake disorders C3489393 Hiatal hernia HSDN C0424755 Fever symptoms C0019326 Ventral hernia HSDN C0233844 Awkwardness C1864706 Myopathy, distal 3 MalaCards|UMLS C0162835 Hypopigmentation C0036489 Sea-blue histiocyte syndrome MalaCards|HPO C3641756 Have diarrhea C0011881 Diabetic nephropathy HSDN C0011570 Monopolar depression C0012236 Digeorge syndrome MalaCards C0020673 Hypothermia (central) (local) C0025063 Mediastinal neoplasms HSDN C3539890 Pelvic pain causes awakening at night C0037274 Dermatologic disorders HSDN C0009080 Finger clubbing C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C0000727 Abdomen acute C0035436 Rheumatic fever HSDN C4084784 Diarrhea C0035333 Retinitis HSDN C1963281 Vomiting adverse event C0005944 Metabolic bone disorder HSDN C2911645 Weight loss adverse event C0038579 Substance abuse, intravenous HSDN C0262977 Decoloration skin C3665492 Structure showing abnormal deposition of pigment (morphologic abnormality) UMLS C0004134 Dyssynergia C3280977 Spastic ataxia 5, autosomal recessive UMLS C2219809 Generalized muscle wasting C0026846 Muscular atrophy UMLS C0026826 High muscle tone C0406740 Kohlschutter tonz syndrome MalaCards C0036572 Convulsion C0006434 Burn injury HSDN C0007758 Cerebellar ataxia C0032965 Pregnancy complications, infectious HSDN C0018784 Deafness sensorineural C1850553 Nephropathy deafness hyperparathyroidism OrphaNet|MalaCards C1549543 Administration method - pain C0040422 Tonsillar neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014356 Enterocolitis HSDN C0917816 Deficiency mental C3806746 Mental retardation, x-linked 99 MalaCards C0007758 Cerebellar ataxia C0029340 Orthomolecular therapy HSDN C0011991 Loose stools C0029408 Degenerative polyarthritis HSDN C4084784 Diarrhea C0024236 Lymphedema HSDN C2919142 Short stature adverse event C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0004604 Pain back C0003090 Ankylosis HSDN C0010520 Skin cyanosis C1527348 Brain hypoxia HSDN C0575081 Abnormal gait C1832334 Charcot-marie-tooth disease, type 4d MalaCards|HPO C0026884 Muteness C0018674 Head trauma HSDN C3539896 Pelvic pain occurs with urination C0227791 Discharge vaginal HSDN C1963091 Diarrhea adverse event C0022890 Labyrinthine disorder HSDN C0014591 Bleeding nose C1260386 Glucocorticoid-remediable aldosteronism HPO C3641756 Have diarrhea C0022680 Polycystic kidney diseases HSDN C0162835 Hypopigmentation C1847024 Albinism, oculocutaneous, type ib (disorder) OrphaNet|HPO|MalaCards C0008031 Pain chest C0019069 Hemophilia a HSDN C0026838 Spasticity muscle C0398746 Gluthathione synthetase deficiency MalaCards C2242996 Tingling C0043251 Wounds and injuries HSDN C0030794 Pelvis pain C0041952 Uerterolithiasis HSDN C0012833 Dizzy C0747122 Pacemaker ddd UMLS C0034150 Skin purpura C0870082 Hyperkeratosis HSDN C0023380 Lethargy C0334663 Histiocytic sarcoma HSDN C0035078 Failure kidney C3495801 Granulomatosis with polyangiitis MalaCards|HPO C0013362 Dysarthrias C3501858 Muscular dystrophy, limb-girdle, type 1d MalaCards C1527344 Dysphonia C0751336 Distal muscular dystrophies HSDN C0085632 Listlessness C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C0027497 Queasy C0878544 Cardiomyopathies HSDN C0030193 Sense of pain C1335452 Adenoid cystic carcinoma of base of tongue UMLS C2919142 Short stature adverse event C2675229 Ciliary dyskinesia, primary, 11 MalaCards|HPO C0020538 Hbp C2676191 Pituitary adenoma, familial isolated (disorder) HPO C0700078 Deep tendon reflex decrease C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C1557397 Adverse event associated with pain C0022367 Jaw, edentulous, partially HSDN C1961131 Cough adverse event C3809651 Infantile liver failure syndrome 2 MalaCards C0003811 Cardiac rhythm disturbance C0011644 Scleroderma OrphaNet|MalaCards C0040264 Ear ringing sound C0149931 Migraine disorders HSDN C1963281 Vomiting adverse event C0266209 Congenital dilatation of colon MalaCards C2919142 Short stature adverse event C0220769 Fg syndrome MalaCards|HPO C0000727 Abdomen acute C3203359 Rupture HSDN C4085548 Usual severity dizziness C0001418 Adenocarcinoma HSDN C0013428 Painful urination C0020295 Hydronephrosis HSDN C0027497 Queasy C0232488 Abdominal colic HSDN C0151889 Reflexes tendon increased C0751748 Nonketotic hyperglycinemia MalaCards|HPO C4085317 Diarrhea frequency C0007527 Cecal disease HSDN C0150055 Pain chronic C0919267 Ovarian neoplasm HSDN C4084802 Usual severity diarrhea C0019693 Hiv infections DiseaseOntology|HSDN|MalaCards C1962972 Proteinuria adverse event C0018946 Hematoma, subdural HSDN C1963184 Nystagmus adverse event C3697269 15q24 microdeletion HPO C0042963 Symptoms vomiting C0175694 Smith-lemli-opitz syndrome MalaCards|HPO|UMLS C0022346 Yellow skin C0016470 Food allergy HSDN C2919142 Short stature adverse event C0238590 Acrogeria OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0018194 Giant cell granuloma HSDN C2984058 Have pain C0234421 Conscious HSDN C0013604 Edematous C1290398 Cerebral arterial aneurysm HSDN C2984058 Have pain C0019310 Hernia, obturator HSDN C0426579 Anorexia symptom C0333355 Inflammatory disease of mucous membrane HSDN C0018524 Hallucinate C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C3163620 Hypotension adverse event C0345904 Malignant neoplasm of liver MalaCards C1549543 Administration method - pain C0015300 Exophthalmos HSDN C2032395 Pelvic pain on the left C0007137 Squamous cell carcinoma HSDN C0017181 Gastrointestinal bleed C0043398 Yellow fever, urban MalaCards C2029884 Hearing loss by exam C0700327 Clinical findings relating to memory HSDN C0020796 Profoundly mentally retarded C0026705 Mucopolysaccharidosis ii OrphaNet C0030552 Paralysis partial C0009475 Community mental health service HSDN C0000737 Abdomen pain C1547940 Specimen source codes - ulcer HSDN C0557874 Global developmental delay C0220687 Kbg syndrome MalaCards|HPO C0013404 Respiratory difficulty C1708782 Signet ring cell carcinoma of lung UMLS C0587050 Lower extremity mass C0238866 Buttock granuloma UMLS C0520966 Coordination impaired C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0018777 Deafness, conductive C0796117 Pitt syndrome MalaCards C0278114 Paraplegia, cerebral C0030486 Paraplegia UMLS C0042963 Symptoms vomiting C0020579 Hypervitaminosis a HSDN C1963071 Back pain adverse event C0015726 Focused anxiety HSDN C2242996 Tingling C0042338 Herpesvirus 3, human HSDN C3539892 Pelvic pain in front C0002871 Anemia HSDN C4084802 Usual severity diarrhea C0001815 Primary myelofibrosis HSDN C4084767 Bothered by vomiting C0702166 Acne HSDN C0024312 Lymphocytopenia C0023240 Legionellosis MalaCards C0031911 Pigment deposition C1336905 Endometrial endometrioid adenocarcinoma MalaCards C0037763 Spasm C0008626 Congenital chromosomal disease HSDN C0024031 Back pain lower back C0033873 Psychiatry HSDN C0011991 Loose stools C0003851 Arteriosclerosis obliterans HSDN C0027497 Queasy C3839212 Familial hyperaldosteronism type 2 MalaCards C0012569 Double vision C0021890 Intraoperative complications HSDN C0030193 Sense of pain C0344479 Spinal cord myelodysplasia HSDN C0221752 Rbc urine C0027341 Nail-patella syndrome MalaCards|HPO C4084768 Usual severity vomiting C0033953 Psychosexual disorders HSDN C4084784 Diarrhea C0014038 Encephalitis HSDN C1963249 Tinnitus adverse event C0021053 Immune system diseases HSDN C4084724 Usual severity constipation C0025289 Meningitis HSDN C0003113 Anomia C0032787 Postoperative complications HSDN C0423572 Needles pin sensation C0030554 Paresthesia UMLS C4084776 Weight loss C1335686 Neuroendocrine neoplasm of rectum MalaCards C0018681 Headache, cephalalgia C0040427 Tooth abnormalities HSDN C0030193 Sense of pain C0031121 Neuralgia peripheral UMLS C1549543 Administration method - pain C0030470 Paranasal sinus neoplasms HSDN C2132198 Abnormal blistering of the skin C0079294 Epidermolysis bullosa dystrophica OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0014474 Ependymoma HSDN C0151786 Weakness muscle C0751873 Demyelinating autoimmune diseases, cns HSDN C3898969 Have been vomiting C1623041 Breast-fed HSDN C4085642 Level of joint stiffness C0002066 Alkaptonuria OrphaNet|HPO|MalaCards C0028961 Urine output decreased C0026764 Multiple myeloma HSDN C0030193 Sense of pain C0497552 Congenital neurologic anomalies HSDN C0023015 Language handicap C0026598 Movement perception HSDN C3815497 Cough C0018133 Graft-vs-host disease HSDN C0007398 Catatonic C0022336 Creutzfeldt-jakob disease HSDN C4084774 Have weight loss C0038436 Post-traumatic stress disorder HSDN C0036572 Convulsion C0080179 Vertebra fracture HSDN C0011991 Loose stools C0042131 Uterine diseases HSDN C0042798 Vision dim C0027832 Neurofibromatosis 2 HPO C3541349 Syncope C0597109 Nurse's role HSDN C4085211 Pain distress question C0238198 Gastrointestinal stromal tumors HSDN C0332573 Macula C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet C0151603 Edema generalized C0279607 Adult primary hepatocellular carcinoma MalaCards C0018965 Blood urine C0024525 Malacoplakia MalaCards C4085211 Pain distress question C0002895 Anemia, sickle cell OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024841 Matrimony, matrimonial HSDN C2032395 Pelvic pain on the left C0033873 Psychiatry HSDN C4084726 Distress cough C0022810 Disease, kyasanur forest MalaCards C0008031 Pain chest C1709578 Pleural sarcomatoid mesothelioma UMLS C4085661 Usual severity nausea C2827407 Infectious otitis media HSDN C0518090 Frequency of pain question C0020428 Hyperaldosteronism HSDN C0004604 Pain back C0007361 Cat-scratch disease DiseaseOntology|MalaCards C1963252 Tremor adverse event C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards|HPO C0012833 Dizzy C0013808 Electroconvulsive therapy HSDN C1962972 Proteinuria adverse event C1522137 Hypertriglyceridemia result HSDN C0026826 High muscle tone C0424688 Small head HSDN C1963137 Hydrocephalus adverse event C1963137 Hydrocephalus adverse event MalaCards C3887873 Hearing loss C0042373 Vascular diseases HSDN C0036396 Sciatica C0860050 Cotunnius' disease UMLS C1384666 Decreased hearing C1859878 Alopecia-mental retardation syndrome 1 MalaCards C0018681 Headache, cephalalgia C0023470 Myeloid leukemia HSDN C4084768 Usual severity vomiting C0015732 Fecal incontinence HSDN C0011570 Monopolar depression C0041408 Turner syndrome MalaCards C0237326 Defecation pain C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C0086437 Joint hypermobility C2750804 Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities MalaCards|HPO|UMLS C2984057 Have nausea C0456892 Csf low pressure HSDN C0151786 Weakness muscle C0453996 Tobacco smoking HSDN C0086439 Activity decreased C1263858 Muscular dystrophy congenital, merosin negative OrphaNet|HPO C2073625 X-ray of chest: pleural effusion C4012050 Hennekam lymphangiectasia-lymphedema syndrome 1 MalaCards C4084725 Usual severity cough C0007273 Carotid artery diseases HSDN C0034933 Abnormal reflexes C0023343 Leprosy HSDN C0042571 Vertigo subjective C0409959 Osteoarthritis, knee HSDN C0741991 Carpometacarpal pain C0022408 Arthropathy UMLS C4084775 Usual severity weight loss C0017185 Gastrointestinal neoplasms HSDN C1961131 Cough adverse event C0751674 Lymphangioleiomyomatosis OrphaNet|HSDN|HPO|MalaCards C0020580 Decreased sensation C3178970 Entrapment, pudendal nerve MalaCards C0007398 Catatonic C0517960 Neurological status: consciousness HSDN C3887873 Hearing loss C3463824 Myelodysplastic syndrome HSDN C0039070 Collapse fleeting C0004238 Atrial fibrillation UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0887833 Carcinoma, pancreatic ductal HSDN C3541349 Syncope C0012691 Dislocations HSDN C0011991 Loose stools C3495559 Juvenile arthritis HSDN C0035078 Failure kidney C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C4084774 Have weight loss C0243013 Base learn problems HSDN C0013421 Dystonia C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C0013604 Edematous C0013291 Duodenal neoplasms HSDN C3146279 Coma C0021400 Influenza HSDN C0007859 Pain neck C0026764 Multiple myeloma HSDN C0398650 Idiopathic thrombocytopenia purpura C0026848 Myopathy HSDN C3887873 Hearing loss C0014544 Epilepsy HSDN C0015468 Face pain C0037286 Skin neoplasms HSDN C0013421 Dystonia C1510460 Orofaciodigital syndrome i MalaCards|HPO C0042024 Urine incontinence C0812393 Cancer patients and suicide and depression HSDN C1963087 Constipation adverse event C0305062 Tetanus toxoids HSDN C1963091 Diarrhea adverse event C0235387 Porphyria type syndrome OrphaNet C0003126 Smell loss C2700405 Waardenburg syndrome, type iie HPO C1384666 Decreased hearing C0042830 Perception visual HSDN C0042963 Symptoms vomiting C0038160 Staphylococcal infections HSDN C0038002 Spleen enlargement C1275081 Cardio-facio-cutaneous syndrome HPO C0003079 Pupillary inequality C0024954 Maxillary neoplasms HSDN C4085210 Usual severity pain C0038358 Gastric ulcer HSDN C0917816 Deficiency mental C1876203 Frontonasal dysplasia MalaCards|HPO C0030200 Intractable pain C0009240 Cognition HSDN C1963281 Vomiting adverse event C0032371 Poliomyelitis MalaCards|HSDN C0015672 Decreased energy C0035078 Kidney failure HSDN C4085317 Diarrhea frequency C0005659 Bite sting HSDN C4085222 Nausea C0007273 Carotid artery diseases HSDN C1963071 Back pain adverse event C0022116 Ischemia HSDN C4084784 Diarrhea C0014556 Epilepsy, temporal lobe HSDN C0027796 Neuralgias C1704436 Peripheral arterial diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0008479 Chondrosarcoma HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024198 Lyme disease HSDN C1557397 Adverse event associated with pain C0009373 Colonic diseases HSDN C4084788 Have dizziness C0009375 Colonic neoplasms HSDN C2919142 Short stature adverse event C0733682 Hypophosphatemic rickets, x-linked dominant OrphaNet|HPO|MalaCards C4084776 Weight loss C0029463 Osteosarcoma HSDN|HPO C0023012 Delay language C0795949 Galloway mowat syndrome HPO C0004134 Dyssynergia C2984299 Asthma pathway HSDN C3827868 Tachycardia by ecg finding C0016756 Fructose-1,6-diphosphatase deficiency MalaCards|HPO C2984058 Have pain C1522137 Hypertriglyceridemia result HSDN C1963063 Anorexia adverse event C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0039070 Collapse fleeting C0085576 Iron-refractory iron deficiency anemia UMLS C4085210 Usual severity pain C0041955 Ureteral neoplasms HSDN C0004310 Auditory disorder process C1510586 Autism spectrum disorders HSDN C0000737 Abdomen pain C0343115 Skin mastocytoma MalaCards|HPO C0518090 Frequency of pain question C0022680 Polycystic kidney diseases HSDN C3641756 Have diarrhea C0013418 Abnormal labor HSDN C0085636 Light sensitivity C0339527 Leber congenital amaurosis HSDN|HPO C0086437 Joint hypermobility C2931058 Marfan syndrome type 2 MalaCards C0221170 Stiffness muscle C0270959 Myotonia levior HPO C0003862 Pain joint C0036421 Systemic scleroderma OrphaNet|HSDN|MalaCards C0018772 Deafness C0015814 Femur head necrosis HSDN C0022568 Inflammation corneal C1274788 Atopic keratoconjunctivitis OrphaNet|MalaCards C0041834 Erythematous condition C1860167 Ackerman syndrome MalaCards C0042571 Vertigo subjective C0428953 Ecg infarction myocardial HSDN C1963091 Diarrhea adverse event C0751651 Mitochondrial diseases HSDN C4084774 Have weight loss C0027809 Neurilemmoma HSDN C4085211 Pain distress question C0334531 Mesonephric tumor HSDN C0700590 Diaphoresis excessive C0029411 Osteoarthropathy, primary hypertrophic MalaCards|HPO C0518090 Frequency of pain question C0033885 Psychoanalytic interpretation HSDN C0031911 Pigment deposition C0685938 Malignant neoplasm of gastrointestinal tract MalaCards C0007758 Cerebellar ataxia C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria OrphaNet|UMLS|MalaCards C0030193 Sense of pain C0242891 Injuries teeth HSDN C0027497 Queasy C0268322 Chester-type porphyria HPO C0413252 Hypothermia due to exposure C0085426 Gram-positive bacterial infections HSDN C2237041 Shox gene with short stature C2931162 Blepharophimosis radioulnar synostosis OrphaNet|MalaCards C0221232 Welts C0157741 Idiopathic urticaria UMLS C0003126 Smell loss C3808975 Hypogonadotropic hypogonadism 18 with or without anosmia MalaCards C1963180 Neck pain adverse event C0037286 Skin neoplasms HSDN C1836296 Lower extremity weakness C0796019 Spastic paraplegia 23 (disorder) MalaCards|HPO|UMLS C0518090 Frequency of pain question C0013589 Ectromelia HSDN C0521532 Diaphragmatic weakness C1739094 Foodborne botulism MalaCards C0518090 Frequency of pain question C2188545 Anuria HSDN C2242996 Tingling C0206247 Amyloid neuropathies HSDN C0424755 Fever symptoms C0001430 Adenoma HSDN C2242996 Tingling C0002448 Ameloblastoma HSDN C2024893 Cardiovascular surgery result: fatigue C0239981 Hypoalbuminemia MalaCards C0085128 Cardiac output elevated C0020452 Hyperemia HSDN C0027066 Myoclonic jerking C0270851 Benign neonatal epilepsy HSDN C4084776 Weight loss C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0460137 Push down or depress C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C0497247 Blood pressure elevation C3495801 Granulomatosis with polyangiitis MalaCards|HPO C4084788 Have dizziness C0042338 Herpesvirus 3, human HSDN C0019825 Voice hoarseness C1334655 Mediastinal germ cell tumor UMLS C3898969 Have been vomiting C1845892 Hprt deficiency, neurologic variant HPO C0242936 Center pain C0019061 Hemolytic-uremic syndrome HSDN C0518090 Frequency of pain question C2350521 Gustatory perception HSDN C2242996 Tingling C1865856 Neuropathy, hereditary thermosensitive MalaCards C2237041 Shox gene with short stature C0796232 Bohring syndrome MalaCards C2911645 Weight loss adverse event C1321581 Bezoar disorder HSDN C0232466 Feeding difficulty C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C0018932 Bright red rectal bleeding C2062326 Eosinophilic enteropathy MalaCards C0012569 Double vision C4084909 Depression subordinate domain HSDN C0042798 Vision dim C0220701 Retinitis pigmentosa 1 MalaCards C0398650 Idiopathic thrombocytopenia purpura C2239176 Liver carcinoma HSDN C4084774 Have weight loss C2674051 Inflammatory bowel disease 11 MalaCards C0036572 Convulsion C0751208 Juvenile huntington disease MalaCards C1549543 Administration method - pain C0282550 Persian gulf syndrome HSDN C0426579 Anorexia symptom C4050613 Anxiety scale (basc-2) HSDN C0042963 Symptoms vomiting C0005940 Bone diseases HSDN C0018777 Deafness, conductive C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0518090 Frequency of pain question C0030312 Pancytopenia HSDN C0162835 Hypopigmentation C1848410 Xeroderma pigmentosum, variant type OrphaNet|HPO|MalaCards C0030193 Sense of pain C0013295 Duodenal ulcer HSDN C0011991 Loose stools C0042111 Urticaria pigmentosa OrphaNet|HSDN|MalaCards C1963170 Hypothermia adverse event C0001127 Acidosis, respiratory HSDN C0027066 Myoclonic jerking C0393622 Drug; myoclonus UMLS C0036572 Convulsion C3536741 Discordant ventriculoarterial connection HSDN C1145670 Failure respiratory C1721007 Pachyonychia congenita, type 2 (disorder) MalaCards C4084768 Usual severity vomiting C0040053 Thrombosis HSDN C1963086 Confusion adverse event C0003850 Arteriosclerosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0016542 Foreign body HSDN C3898969 Have been vomiting C0043251 Wounds and injuries HSDN C0025287 Meningitis-like C0026976 Myelitis, transverse HSDN C2024878 Cardiovascular surgery result: dyspnea C0014116 Endocardial cushion defects HSDN C0015676 Mental fatigue C0038454 Cerebrovascular accident HSDN C0020538 Hbp C0342200 Endemic cretinism MalaCards C3463815 Feel fatigue C0814263 Meditation therapy HSDN C4085222 Nausea C0005891 Bodies image HSDN C0013404 Respiratory difficulty C2239112 Blister dosing unit HSDN C0003862 Pain joint C0035436 Rheumatic fever OrphaNet|HSDN|MalaCards C3665347 Vision impaired C3495589 Jalili syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C0030305 Pancreatitis HSDN C0043068 Friderichsen-waterhouse syndrome C2586211 Thrombosis of blood vessel HSDN C1963087 Constipation adverse event C3178970 Entrapment, pudendal nerve MalaCards C0026838 Spasticity muscle C3149907 Als13 HPO C3146279 Coma C4042784 Feeding and eating disorders HSDN C3463815 Feel fatigue C0334419 Pheochromocytoma, malignant MalaCards C3665347 Vision impaired C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards|HPO C3641756 Have diarrhea C0162627 Skin diseases, bacterial HSDN C0004604 Pain back C0035439 Rheumatic heart disease HSDN C0011206 Delirium acute C0021799 Interprofessional relations HSDN C4084774 Have weight loss C1321581 Bezoar disorder HSDN C0413252 Hypothermia due to exposure C0460137 Push down or depress HSDN C0917816 Deficiency mental C2931294 Wiedemann grosse dibbern syndrome MalaCards C1384666 Decreased hearing C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084775 Usual severity weight loss C0024232 Lymphatic metastasis HSDN C0009421 Comatose C1704972 Genomic orientation HSDN C0565404 Premature or threatened labor C0022876 Premature obstetric labor UMLS C1836296 Lower extremity weakness C1854568 Spastic paraplegia 14, autosomal recessive (disorder) MalaCards|UMLS C4085548 Usual severity dizziness C1962958 Hematoma adverse event HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0206366 Ossification of posterior longitudinal ligament HSDN C3665347 Vision impaired C3150801 Combined oxidative phosphorylation deficiency 7 MalaCards|HPO C4085317 Diarrhea frequency C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0042850 Vitamin b deficiency HSDN C0030193 Sense of pain C0263866 Lumbago or sciatica due to displacement of intervertebral disc UMLS C0036572 Convulsion C0015395 Burn eye HSDN C0242936 Center pain C0206754 Neuroendocrine tumors HSDN C0002962 Angina C0027765 Nervous system disorder HSDN C1963087 Constipation adverse event C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C1963065 Apnea adverse event C1290398 Cerebral arterial aneurysm HSDN C0332563 Papulae C0268381 Primary amyloidosis MalaCards C0011570 Monopolar depression C0795959 Gomez lopez hernandez syndrome MalaCards C0242936 Center pain C0393571 Multiple system atrophy HSDN C0002962 Angina C1705810 Generic role HSDN C0030552 Paralysis partial C0162672 Merrf syndrome MalaCards|HSDN|HPO C0030193 Sense of pain C0039520 Tenosynovitis HSDN C0022346 Yellow skin C2609268 Low phospholipid-associated cholelithiasis MalaCards C3146279 Coma C0014859 Esophageal neoplasms HSDN C0009421 Comatose C0349464 Wernicke-korsakoff syndrome MalaCards C2984057 Have nausea C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0497406 Over weight C0028758 Bonding HSDN C4084725 Usual severity cough C0348018 Projections HSDN C3146279 Coma C0027439 Nasopharyngeal neoplasms HSDN C0917816 Deficiency mental C3889474 Bardet-biedl syndrome 16 MalaCards C0013404 Respiratory difficulty C4042784 Feeding and eating disorders HSDN C0022346 Yellow skin C0278699 Childhood hepatoma, group iv UMLS C4085317 Diarrhea frequency C0024138 Lupus erythematosus, discoid HSDN C0018775 Hearing loss bilateral C1824925 Deafness, autosomal recessive 70 MalaCards C0019572 Hairiness C1720863 Congenital generalized lipodystrophy type 2 MalaCards|HPO C1856661 Cornea cloudy C1848410 Xeroderma pigmentosum, variant type MalaCards C0009024 Clonus C1836522 Schindler disease, type ii MalaCards C1963071 Back pain adverse event C0014547 Epilepsies, partial HSDN C0030193 Sense of pain C0750394 Wbc low HSDN C0013405 Dyspnea, paroxysmal C0024630 Malingering HSDN C0015970 Fever unknown origin C0025202 Melanoma HSDN C0019079 Bloody sputum C4085311 Depression - recess HSDN C0085650 Purpura fulminans C0038395 Streptococcal infections HSDN C0042940 Disorder of voice C0002736 Amyotrophic lateral sclerosis HSDN C4085211 Pain distress question C0043168 Whooping cough due to unspecified organism HSDN C0036659 Sensation disorder C0021655 Insulin resistance HSDN C0413252 Hypothermia due to exposure C0023798 Lipoma HSDN C0042963 Symptoms vomiting C0001144 Acne vulgaris HSDN C0026838 Spasticity muscle C0002940 Aneurysm HSDN C0042571 Vertigo subjective C0031090 Periodontal diseases HSDN C4084724 Usual severity constipation C0220769 Fg syndrome MalaCards|HPO C0015230 Exanthem C0277367 Allergic skin reaction due to sand fly bite UMLS C2911645 Weight loss adverse event C0014863 Esophageal spasm diffuse HSDN C2315100 Pediatric failure to thrive C3150172 Mtdps8b MalaCards|HPO C1579931 Depressed - symptom C1568249 Usher syndrome, type ii MalaCards|HPO C4084802 Usual severity diarrhea C0015734 Stool impacted HSDN C4084788 Have dizziness C0018799 Heart diseases HSDN C0013362 Dysarthrias C0028738 Nystagmus HSDN C0043094 Weight gain C0042580 Vesico-ureteral reflux HSDN C3665386 Abnormal vision C0220658 Pfeiffer syndrome MalaCards C1549543 Administration method - pain C3714644 Thymus neoplasms HSDN C0012833 Dizzy C3280866 Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) MalaCards C4085211 Pain distress question C0015404 Eye infections, bacterial HSDN C1384666 Decreased hearing C1866649 Steinfeld syndrome MalaCards C1268578 Palatal paresis C0221060 Mobius syndrome MalaCards|UMLS C4084766 Vomiting C0040336 Tobacco use disorder HSDN C4084768 Usual severity vomiting C0043515 Zollinger-ellison syndrome HSDN C3463815 Feel fatigue C0029458 Osteoporosis, postmenopausal HSDN C1963137 Hydrocephalus adverse event C1956093 Paris-trousseau thrombocytopenia MalaCards C0155552 Hearing loss mixed C2931244 Craniometaphyseal dysplasia, autosomal recessive type MalaCards C3146279 Coma C1859974 Glucocorticoid deficiency 1 HPO C4084784 Diarrhea C0031069 Familial mediterranean fever OrphaNet|HPO C0036572 Convulsion C1333630 Foramen magnum meningioma UMLS C0013428 Painful urination C0333596 Deposition of iron HSDN C0040822 D tremors C1866552 Paragangliomas 2 (disorder) MalaCards C0004134 Dyssynergia C0022660 Kidney failure, acute HSDN C0007815 Cerebrospinal fluid rhinorrhoea C1306214 Acth-secreting pituitary adenoma HSDN C2911645 Weight loss adverse event C0031117 Peripheral neuropathy HSDN C4084788 Have dizziness C0014055 Encephalitis, epidemic HSDN C1557397 Adverse event associated with pain C0019195 Hepatitis, viral, human HSDN C2032396 Pelvic pain on the right C0006434 Burn injury HSDN C0008031 Pain chest C0009938 Bruising HSDN C1963071 Back pain adverse event C3495422 Finding relating to sexuality and sexual activity HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0009326 Collagen diseases HSDN C4084775 Usual severity weight loss C0002170 Alopecia HSDN C3541349 Syncope C3812141 Linc00914 gene HSDN C1971624 Appetite absent C1848561 Methylmalonic acidemia with homocystinuria MalaCards C0004134 Dyssynergia C0795889 Allan-herndon-dudley syndrome (ahds) OrphaNet|UMLS|HPO|MalaCards C0020450 Hyperemesis gravidarum C0020625 Hyponatremia HSDN C0013362 Dysarthrias C0751278 Metachromatic leukodystrophy, infant MalaCards|HPO C0016382 Cutaneous vascular engorgement C0580181 Benign lymphocytic infiltration of jessner OrphaNet C4084776 Weight loss C0042075 Urologic diseases HSDN C3494358 Characteristic, prodromal C4084909 Depression subordinate domain HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029421 Osteochondritis dissecans HSDN C0003862 Pain joint C4225189 Microcephaly, congenital cataract, and psoriasiform dermatitis UMLS C2029884 Hearing loss by exam C0000768 Congenital abnormality HSDN C1090821 Sepsis C3661525 Autosomal recessive chronic granulomatous disease MalaCards C2364111 Gustatory anesthesia C0051981 Anti-leprosy vaccine HSDN C3887873 Hearing loss C0796279 Carnevale syndrome MalaCards C0036396 Sciatica C0518450 Spinal fractures HSDN C4085862 Bothered by nausea C2981150 Uranostaphyloschisis HSDN C0008031 Pain chest C2828211 Stage ib pleural mesothelioma UMLS C0015230 Exanthem C0342337 Insulin resistance syndrome, type b MalaCards C0026838 Spasticity muscle C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C4084776 Weight loss C0086438 Hypogammaglobulinemia MalaCards C0038990 Sweats C0271889 Diencephalic syndrome of infancy OrphaNet|MalaCards C4084776 Weight loss C1266101 Thymic epithelial tumor OrphaNet C4084725 Usual severity cough C0032231 Pleurisy HSDN C0040822 D tremors C0268242 Niemann-pick disease, type a MalaCards|HSDN C3274924 Have been coughing C0021831 Intestinal diseases HSDN C2911645 Weight loss adverse event C0027092 Myopia HSDN C0040822 D tremors C0041327 Tuberculosis, pulmonary HSDN C4084725 Usual severity cough C1000587 Pemphigus HSDN C0028738 Nystagmus C0268505 Ocular albinism, type ii OrphaNet|HPO|MalaCards C0041667 Low weight C3714896 Smith-mccort dysplasia 2 MalaCards C0018772 Deafness C0034735 Raynaud phenomenon HSDN C1279888 Proteinuria of undiagnosed cause C0029400 Osteitis HSDN C0424755 Fever symptoms C0039730 Thalassemia HSDN C0018772 Deafness C1855126 3-methylglutaconic aciduria type iv MalaCards C1000483 Genus anemia C1839161 Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis MalaCards C0000737 Abdomen pain C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome MalaCards C0025323 Bleeding menstrual heavy C1282971 Von willebrand disease, type 2b HPO C2169806 Tic C0031350 Pharyngitis HSDN C2911645 Weight loss adverse event C0038463 Strongyloides infection HSDN C0006271 Inflammation of the bronchioles C1858266 Bare lymphocyte syndrome, type i MalaCards|HPO C4085210 Usual severity pain C0024693 Mandible injury HSDN C3463815 Feel fatigue C2919115 Encounter due to bereavement HSDN C4084726 Distress cough C0264353 Bronchomalacia HSDN C4085210 Usual severity pain C0860239 Catheter infections related HSDN C0013404 Respiratory difficulty C0023895 Liver diseases HSDN C0012833 Dizzy C1832600 Naxos disease OrphaNet|HPO|MalaCards C0020438 Hypercalciuria C0008533 Hemophilia b HSDN C0242936 Center pain C0002453 Amenorrhea HSDN C0009792 Consciousness disorder C0011860 Diabetes mellitus, non-insulin-dependent HSDN C1963091 Diarrhea adverse event C0003857 Congenital arteriovenous malformation HSDN C1549543 Administration method - pain C0007867 Cervix diseases HSDN C3146279 Coma C0237873 Physiological sexual disorders HSDN C0027424 Congestion nasal C4015016 Ciliary dyskinesia, primary, 30 MalaCards C1963087 Constipation adverse event C0205788 Histiocytoid hemangioma HSDN C0023012 Delay language C0750927 Apraxia, developmental verbal HPO C4084774 Have weight loss C0040136 Thyroid neoplasm HSDN C1145670 Failure respiratory C0085435 Arthritis, reactive MalaCards C2237041 Shox gene with short stature C1853271 Hypophosphatemic rickets with hypercalciuria, hereditary OrphaNet|HPO C4084768 Usual severity vomiting C0206255 Malaria vaccine HSDN C0034151 Hyperglobulinemic purpura C0010674 Cystic fibrosis HSDN C0000731 Abdomen distention C2746068 Congenital idiopathic intestinal pseudoobstruction MalaCards|HPO C2237041 Shox gene with short stature C1848336 Dent disease 1 HPO C0476273 Distress respiratory C0035934 Rubinstein-taybi syndrome HPO C0012833 Dizzy C0010823 Cytomegalovirus infections HSDN C0042384 Vasculitis, nonspecific C0032533 Polymyalgia rheumatica MalaCards C0578737 Brachial lymphadenopathy C0578735 Axillary lymphadenopathy UMLS C4085317 Diarrhea frequency C0039082 Syndrome HSDN C0751495 Seizure focal C0917800 Epilepsy, myoclonic, infantile UMLS C0009676 Confusion state C0040046 Thrombophlebitis HSDN C0000737 Abdomen pain C2212006 Ovarian small cell carcinoma UMLS C0270948 Neurogenic muscular atrophy C1850746 Carey-fineman-ziter syndrome OrphaNet C4085211 Pain distress question C0037937 Spine injury HSDN C0001825 Agraphia C0338451 Frontotemporal dementia HSDN C0398650 Idiopathic thrombocytopenia purpura C0016542 Foreign body HSDN C0233763 Hallucinations visual C1851958 Lewy body variant of alzheimer disease HPO C4085210 Usual severity pain C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C2242996 Tingling C0004623 Bacterial infections HSDN C0030975 Disorders perception C0013712 Ego HSDN C0012833 Dizzy C0206734 Hemangioblastoma MalaCards C0237326 Defecation pain C0220769 Fg syndrome MalaCards|HPO C0030486 Extremity paralysis, lower C0022738 Klippel-feil syndrome HSDN C4084773 Bothered by weight gain C0040038 Thromboembolism HSDN C1557397 Adverse event associated with pain C0031190 Persistent fetal circulation syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011609 Drug eruptions HSDN C0036572 Convulsion C0268226 Type i mucolipidosis OrphaNet|HPO C1963281 Vomiting adverse event C0021603 Sleep initiation and maintenance disorders HSDN C1963091 Diarrhea adverse event C0025294 Meningococcal meningitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016879 Fusobacterium infections HSDN C1963281 Vomiting adverse event C0043254 Injuries penetrating HSDN C0011991 Loose stools C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C1963091 Diarrhea adverse event C0001125 Acidosis, lactic HSDN C0024312 Lymphocytopenia C0043194 Wiskott-aldrich syndrome OrphaNet|HPO|MalaCards C1384666 Decreased hearing C1527231 Adrenomyeloneuropathy MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0017636 Glioblastoma MalaCards|HSDN C4085642 Level of joint stiffness C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0752235 Lyme neuroborreliosis HSDN C4084784 Diarrhea C1801959 Histiocytic medullary reticulosis (disorder) MalaCards|HPO C1963184 Nystagmus adverse event C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C3898969 Have been vomiting C1563705 Nephrogenic diabetes insipidus, type i HPO C2919142 Short stature adverse event C0796142 Sao paulo mca-mr syndrome MalaCards C0004604 Pain back C0270611 Brain damage HSDN C0013528 Echo speech C0033927 Psychopathology HSDN C4084724 Usual severity constipation C0305062 Tetanus toxoids HSDN C1557397 Adverse event associated with pain C0043048 Experimental water deprivation HSDN C1963087 Constipation adverse event C0003507 Aortic valve stenosis HSDN C2911645 Weight loss adverse event C0033968 Psychotherapeutic technique HSDN C0003862 Pain joint C0018536 Hallux valgus disorder HSDN C0027066 Myoclonic jerking C0751779 Action myoclonus-renal failure syndrome HPO C3146279 Coma C0041374 Tumor virus infections HSDN C1384666 Decreased hearing C1842371 Deafness, autosomal dominant 41 (disorder) MalaCards|HPO C0860603 Anxiety symptom C0001206 Acromegaly OrphaNet|HPO|MalaCards C3146279 Coma C0702166 Acne HSDN C3641755 Have constipation C0009324 Ulcerative colitis HSDN C3274924 Have been coughing C0017416 Genital neoplasms, female HSDN C1971624 Appetite absent C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0043094 Weight gain C1720777 Functional laterality HSDN C3887638 Failure to thrive in infant C2677434 Orofacial cleft 11 MalaCards C0557874 Global developmental delay C1868570 Char syndrome MalaCards|HPO C4085210 Usual severity pain C0948089 Acute coronary syndrome HSDN C4084726 Distress cough C0014850 Esophageal atresia HSDN C0042571 Vertigo subjective C0001818 Agoraphobia HSDN C2032396 Pelvic pain on the right C0034065 Pulmonary embolism HSDN C0035078 Failure kidney C1857388 Cystinuria, type a HPO C0039070 Collapse fleeting C0024841 Matrimony, matrimonial HSDN C0027498 Nausea vomiting C2931916 Midline granulomatosis MalaCards C0020538 Hbp C0282492 Sneddon syndrome OrphaNet|HPO|MalaCards C0013428 Painful urination C1519915 Vaginal adenosquamous carcinoma UMLS C0018772 Deafness C0002880 Autoimmune hemolytic anemia HSDN C0151889 Reflexes tendon increased C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C0018775 Hearing loss bilateral C0041296 Tuberculosis HSDN C4084767 Bothered by vomiting C0018799 Heart diseases HSDN C3463815 Feel fatigue C0035243 Respiratory tract infections HSDN C0024031 Back pain lower back C0029928 Ovarian diseases HSDN C0344428 Ventricular tachycardia by ecg finding C1735340 Multifocal ventricular extrasystoles MalaCards C1384666 Decreased hearing C0265341 Rieger syndrome OrphaNet|HPO C4084784 Diarrhea C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C0026821 Cramp C0002871 Anemia HSDN C0812426 Kidney problem C0848548 Hypertensive nephropathy UMLS C0015970 Fever unknown origin C0023467 Leukemia, myelocytic, acute HSDN C4085661 Usual severity nausea C0016751 Hereditary fructose intolerance syndrome HPO C4084774 Have weight loss C0033805 Pseudohypoaldosteronism HSDN C0042571 Vertigo subjective C3827868 Tachycardia by ecg finding HSDN C4084775 Usual severity weight loss C0025007 Measles HSDN C1963252 Tremor adverse event C2698658 Orofaciodigital syndrome type 1 MalaCards C4085211 Pain distress question C0339289 Injury corneal HSDN C3539896 Pelvic pain occurs with urination C0033038 Ejaculatio praecox HSDN C1963184 Nystagmus adverse event C4041558 Cone-rod synaptic disorder, congenital nonprogressive MalaCards C0231835 Respiration rate increased C0242188 Spider bites HSDN C4084767 Bothered by vomiting C1579931 Depressed - symptom HSDN C1549543 Administration method - pain C1962962 Hyperpigmentation adverse event HSDN C0015672 Decreased energy C0002940 Aneurysm HSDN C0026821 Cramp C1550639 Specimen type - fistula HSDN C4084784 Diarrhea C0162703 Pain sensitivity HSDN C0035078 Failure kidney C1866075 Glomerulopathy with fibronectin deposits 2 (disorder) OrphaNet|HPO|MalaCards C1963071 Back pain adverse event C0038644 Sudden infant death syndrome HSDN C0015469 Facial paralysis C0007274 Carotid artery thrombosis HSDN C4085222 Nausea C0007784 Cerebral hemisphere hemorrhage HSDN C0242936 Center pain C0010701 Phyllodes tumor HSDN C0013604 Edematous C0038525 Subarachnoid hemorrhage HSDN C0242936 Center pain C0040422 Tonsillar neoplasms HSDN C4085317 Diarrhea frequency C0272129 Donath-landsteiner hemolytic anemia MalaCards C0860603 Anxiety symptom C1858501 Spinocerebellar ataxia 12 MalaCards|HPO C3539890 Pelvic pain causes awakening at night C2936290 Femoracetabular impingement HSDN C4084774 Have weight loss C0006277 Bronchitis HSDN C0424755 Fever symptoms C1850635 Atrial myxoma, familial MalaCards C2315100 Pediatric failure to thrive C0006287 Bronchopulmonary dysplasia HSDN C0036572 Convulsion C3808397 Cortical dysplasia, complex, with other brain malformations 1 MalaCards C3539020 Pelvic pain decreasing in frequency C1299262 Sarcoma - category (morphologic abnormality) HSDN C1549543 Administration method - pain C0018805 Heart injuries HSDN C4085211 Pain distress question C0003827 Art therapies HSDN C1260880 Nasal drip C1336434 Paranasal sinus cancer stage iv UMLS C0557874 Global developmental delay C1857780 Joubert syndrome 5 MalaCards C1963184 Nystagmus adverse event C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C2911645 Weight loss adverse event C0033054 Prenatal exposure delayed effects HSDN C0039070 Collapse fleeting C1735340 Multifocal ventricular extrasystoles MalaCards C3665386 Abnormal vision C1848639 Ush1a, formerly HPO C0020673 Hypothermia (central) (local) C0242231 Coronary stenosis HSDN C4084769 Vomiting frequency C0036095 Salivary gland neoplasms HSDN C2919142 Short stature adverse event C0432269 Lenz majewski hyperostotic dwarfism MalaCards|HPO C0009806 Constipate C0001973 Alcoholic intoxication, chronic HSDN C4084776 Weight loss C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|HSDN|MalaCards C4085210 Usual severity pain C0011351 Dental enamel hypoplasia HSDN C0242936 Center pain C0039132 Cutaneous syphilis HSDN C3463815 Feel fatigue C0025268 Multiple endocrine neoplasia type 2a OrphaNet C2911645 Weight loss adverse event C0085655 Polymyositis OrphaNet|MalaCards C1963249 Tinnitus adverse event C0027858 Neuroma HSDN C1527344 Dysphonia C0033968 Psychotherapeutic technique HSDN C0742281 Chest pain angina C0741025 Chest problem UMLS C0013595 Eczematous dermatitis C1956093 Paris-trousseau thrombocytopenia MalaCards C1963091 Diarrhea adverse event C0087130 Uncertain HSDN C0020673 Hypothermia (central) (local) C0034067 Pulmonary emphysema HSDN C1384666 Decreased hearing C0026709 Mucopolysaccharidosis vi OrphaNet|HPO|MalaCards C4084774 Have weight loss C0022665 Kidney neoplasm HSDN C0020580 Decreased sensation C2749345 Refsum disease, adult, 1 HPO C0242936 Center pain C0012817 Diverticulum HSDN C4085317 Diarrhea frequency C0042134 Uterine hemorrhage HSDN C1384666 Decreased hearing C0038379 Eye deviation HSDN C0042963 Symptoms vomiting C0016751 Hereditary fructose intolerance syndrome HSDN|HPO|UMLS C1963065 Apnea adverse event C0004415 Aversion therapy HSDN C2203646 Jaundice C0520946 Emotional hypersensitivity HSDN C0036572 Convulsion C0014836 Escherichia coli infections HSDN C3887638 Failure to thrive in infant C0008066 Child behavior disorders HSDN C0018772 Deafness C0015726 Focused anxiety HSDN C0039070 Collapse fleeting C0242707 Ventricular dysfunction, right HSDN C0036572 Convulsion C0030470 Paranasal sinus neoplasms HSDN C0242936 Center pain C0036875 Disorders of sex development HSDN C1962972 Proteinuria adverse event C1963059 Adrenal insufficiency adverse event HSDN C1963071 Back pain adverse event C0018213 Graves disease HSDN C0004604 Pain back C0040046 Thrombophlebitis HSDN C0007814 Cerebrospinal fluid otorrhea C0020255 Hydrocephalus HSDN C0349506 Sun sensitivity C1868311 Piebald trait neurologic defects OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C2937358 Cerebral hemorrhage HSDN C0012833 Dizzy C0019360 Herpes zoster disease HSDN C0035232 Diaphragmatic paralysis C0030567 Parkinson disease HSDN C4084776 Weight loss C0152018 Esophageal carcinoma OrphaNet|MalaCards C0085631 Abnormal excitement C0702221 Tactual discrimination HSDN C4084767 Bothered by vomiting C0752132 Infarction, pca HSDN C0234132 Pyramidal sign C0206641 Osteochondromatosis HPO C0232466 Feeding difficulty C0520681 Central alveolar hypoventilation syndrome MalaCards C3463815 Feel fatigue C0553604 Myotonic disorders HSDN C4084766 Vomiting C0003496 Aortic rupture HSDN C0040264 Ear ringing sound C0206721 Inverted papilloma HSDN C3665492 Pigmentations C1527349 Ductal breast carcinoma MalaCards C0233514 Behavior abnormal C1846707 Spinocerebellar ataxia 17 OrphaNet|HPO|MalaCards C0036572 Convulsion C0431289 Encephalocele, frontal MalaCards C1384666 Decreased hearing C1414529 Fancc gene HPO C3641756 Have diarrhea C1850406 Navajo neurohepatopathy MalaCards|HPO C0042963 Symptoms vomiting C0007193 Cardiomyopathy, dilated HSDN C2029884 Hearing loss by exam C0037928 Spinal cord diseases HSDN C0237326 Defecation pain C0271585 Isolated trh deficiency MalaCards C0030552 Paralysis partial C0035243 Respiratory tract infections HSDN C2984057 Have nausea C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4085210 Usual severity pain C0028433 Nose neoplasms HSDN C3887638 Failure to thrive in infant C0014851 Cyst, esophageal HSDN C0042571 Vertigo subjective C0853697 Neutrophil count decreased HSDN C0426579 Anorexia symptom C0038587 Substance withdrawal syndrome HSDN C0026821 Cramp C0152109 Juvenile spinal muscular atrophy HPO|UMLS C0018784 Deafness sensorineural C1567743 Alport syndrome, autosomal dominant MalaCards|HPO C0036572 Convulsion C0013575 Ectodermal dysplasia MalaCards|HSDN C0587246 Extremity weakness C1836472 Nemaline myopathy 6 HPO C2237041 Shox gene with short stature C1860615 Hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna OrphaNet|MalaCards C0027498 Nausea vomiting C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C0349588 Stature short C0432252 Osteoporosis with pseudoglioma MalaCards|HPO C0022346 Yellow skin C0043397 Yellow fever, jungle MalaCards C0344315 Mood depressed C0175702 Williams syndrome OrphaNet|HPO|MalaCards C3887873 Hearing loss C0340427 Familial dilated cardiomyopathy MalaCards C2032396 Pelvic pain on the right C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0038002 Spleen enlargement C0024899 Mastocytosis MalaCards C1549543 Administration method - pain C0040409 Tongue diseases HSDN C0349588 Stature short C0432365 Thalidomide embryopathy syndrome OrphaNet|MalaCards C1963091 Diarrhea adverse event C1510412 Pseudoaneurysm HSDN C0018784 Deafness sensorineural C0023308 Lens diseases HSDN C0030975 Disorders perception C0033871 Psychiatric status rating scales HSDN C1384666 Decreased hearing C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C1069915 Vertigo C0024535 Malaria, falciparum HSDN C0150055 Pain chronic C0038587 Substance withdrawal syndrome HSDN C4085548 Usual severity dizziness C0002989 Epithelioid hemangioma of skin HSDN C4085210 Usual severity pain C0018213 Graves disease HSDN C0020673 Hypothermia (central) (local) C0021368 Inflammation HSDN C4085862 Bothered by nausea C0004096 Asthma HSDN C0030552 Paralysis partial C0085209 Bovine spongiform encephalitis MalaCards C3641756 Have diarrhea C0042900 Vitiligo HSDN C0042963 Symptoms vomiting C0265673 Congenital kyphosis HSDN C0012569 Double vision C0476171 Comminuted HSDN C0022346 Yellow skin C0037974 Spirochaetales infections HSDN C3809715 Epistaxis recurrent C1838163 Osler-rendu-weber syndrome 2 MalaCards|HPO C4084802 Usual severity diarrhea C0027947 Neutropenia HSDN C0003079 Pupillary inequality C0043324 Juvenile xanthogranuloma HSDN C3641756 Have diarrhea C1009209 Tinea HSDN C4085210 Usual severity pain C0039520 Tenosynovitis HSDN C0424755 Fever symptoms C0026857 Musculoskeletal diseases HSDN C0042025 Urinary incontinence stress C0020649 Hypotension HSDN C0019079 Bloody sputum C0265908 Congenital atresia of pulmonary artery HSDN C0595939 Stillborn C0268318 Cholestasis of pregnancy MalaCards C0019079 Bloody sputum C0221390 Non-bacterial thrombotic endocarditis HSDN C0006370 Bulimia C0033923 Psychomotor function HSDN C4084802 Usual severity diarrhea C0008350 Cholelithiasis HSDN C0018681 Headache, cephalalgia C0009450 Disease caused by microorganism HSDN C0243026 Generalized infection C1850406 Navajo neurohepatopathy MalaCards C0013390 Cramps menstrual C4084909 Depression subordinate domain HSDN C4085862 Bothered by nausea C0026848 Myopathy HSDN C0232466 Feeding difficulty C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C0040264 Ear ringing sound C0032962 Pregnancy complications HSDN C2911645 Weight loss adverse event C0001807 Aggressive behavior HSDN C3463815 Feel fatigue C0162651 Gastric outlet obstruction HSDN C0518090 Frequency of pain question C0001144 Acne vulgaris HSDN C0020672 Body temperature decreased C0032343 Poisoning HSDN C0020305 Fetal edema C0002880 Autoimmune hemolytic anemia HSDN C0016382 Cutaneous vascular engorgement C0406645 Amyopathic dermatomyositis MalaCards C4085661 Usual severity nausea C0036916 Sexually transmitted diseases HSDN C2984058 Have pain C0036980 Shock, cardiogenic HSDN C0018681 Headache, cephalalgia C0005967 Bone neoplasms HSDN C0013404 Respiratory difficulty C0032914 Pre-eclampsia HSDN C3146279 Coma C0032002 Pituitary diseases HSDN C0036396 Sciatica C0032019 Pituitary neoplasms HSDN C0029163 Hemorrhage mouth C0017205 Gaucher disease HSDN C0085636 Light sensitivity C0836924 Thrombocytosis HSDN C0027066 Myoclonic jerking C0040188 Tic disorder UMLS C0013428 Painful urination C0036916 Sexually transmitted diseases HSDN C0026205 Pupillary constriction C1565107 Disorder, secondary headache HSDN C0237326 Defecation pain C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C0030193 Sense of pain C0008049 Chicken pox HSDN C0085636 Light sensitivity C1837073 Spondylometaphyseal dysplasia with cone-rod dystrophy OrphaNet|HPO C0018681 Headache, cephalalgia C0037929 Spinal cord injuries HSDN C0036572 Convulsion C1706377 Memory device component HSDN C0085631 Abnormal excitement C0003467 Anxiety UMLS C0014591 Bleeding nose C0032463 Polycythemia vera OrphaNet|HPO C1963170 Hypothermia adverse event C0032969 Pregnancy in diabetics HSDN C1963246 Sinus tachycardia adverse event C0334419 Pheochromocytoma, malignant MalaCards C2242996 Tingling C0024950 Maxillary diseases HSDN C1549543 Administration method - pain C3463897 Hydatidiform mole, recurrent, 1 HSDN C0242936 Center pain C0023601 Leydig cell tumor HSDN C1963281 Vomiting adverse event C0239189 Disaccharide intolerance MalaCards C2911647 Weight gain adverse event C0022658 Kidney diseases HSDN C0234146 Absent reflex C1851708 Encephalopathy, recurrent, of childhood MalaCards C0043094 Weight gain C3495801 Granulomatosis with polyangiitis HSDN C0042571 Vertigo subjective C0023890 Liver cirrhosis HSDN C1963063 Anorexia adverse event C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C0042571 Vertigo subjective C4085311 Depression - recess HSDN C3463815 Feel fatigue C0036983 Septic shock HSDN C3494358 Characteristic, prodromal C0428977 Bradycardia HSDN C0028738 Nystagmus C2931753 Achromatopsia incomplete, x-linked MalaCards C3887638 Failure to thrive in infant C0852654 21-hydroxylase deficiency MalaCards C0004134 Dyssynergia C2931928 Mitochondrial cytopathy MalaCards C0013604 Edematous C0027661 Neoplasms, hormone-dependent HSDN C1963090 Dehydration adverse event C3543867 Collodion fetus MalaCards C0036572 Convulsion C0040422 Tonsillar neoplasms HSDN C0036572 Convulsion C3494506 Pseudohypoparathyroidism, type ia UMLS C0000737 Abdomen pain C0008728 Churg-strauss syndrome OrphaNet|HSDN|MalaCards C2203646 Jaundice C2931004 Congenital disorder of glycosylation type 1j MalaCards C3815497 Cough C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C3539890 Pelvic pain causes awakening at night C0520946 Emotional hypersensitivity HSDN C1963137 Hydrocephalus adverse event C1855923 Hyperphosphatasia with mental retardation MalaCards|HPO C2911645 Weight loss adverse event C0030521 Parathyroid neoplasms MalaCards|HSDN C1860844 Sparse, thin hair C1848392 Zunich neuroectodermal syndrome HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0002994 Angioedema HSDN C1963093 Dizziness adverse event C0029883 Otitis media with effusion HSDN C0042963 Symptoms vomiting C0010823 Cytomegalovirus infections HSDN C4085317 Diarrhea frequency C0018852 Heavy chain disease HSDN C0011991 Loose stools C0032965 Pregnancy complications, infectious HSDN C3815497 Cough C0008325 Cholecystitis HSDN C0040822 D tremors C0036946 Sheep--diseases HSDN C4084788 Have dizziness C0262655 Recurrent urinary tract infection HSDN C0011991 Loose stools C0020875 Ileal diseases HSDN C0151786 Weakness muscle C0007131 Non-small cell lung carcinoma HSDN C0151786 Weakness muscle C3151753 Combined oxidative phosphorylation deficiency 6 MalaCards|UMLS C0034150 Skin purpura C2937287 Hematolysis HSDN C2024893 Cardiovascular surgery result: fatigue C1720777 Functional laterality HSDN C1963071 Back pain adverse event C0001144 Acne vulgaris HSDN C4085210 Usual severity pain C1961100 Erectile dysfunction adverse event HSDN C1963170 Hypothermia adverse event C0040128 Thyroid diseases HSDN C0007758 Cerebellar ataxia C0006118 Brain neoplasms HSDN C0013395 Indigestion C0027059 Myocarditis HSDN C0033377 Caudal displacement C0393929 Familial infantile myasthenia MalaCards|HPO C0036572 Convulsion C0018790 Cardiac arrest UMLS C0018772 Deafness C0039730 Thalassemia HSDN C0231835 Respiration rate increased C1855675 Arima syndrome OrphaNet|HPO|MalaCards C0013421 Dystonia C0034345 Pyruvate dehydrogenase complex deficiency disease MalaCards|HPO C3641756 Have diarrhea C0342793 Malonic aciduria MalaCards|HPO C2364111 Gustatory anesthesia C0026636 Mouth diseases HSDN C0349588 Stature short C3554774 Tyshchenko syndrome MalaCards C0000737 Abdomen pain C0004238 Atrial fibrillation HSDN C1961131 Cough adverse event C0043251 Wounds and injuries HSDN C2911647 Weight gain adverse event C0032019 Pituitary neoplasms HSDN C0019572 Hairiness C0032965 Pregnancy complications, infectious HSDN C0012569 Double vision C0020490 Hyperopia HSDN C0042571 Vertigo subjective C0031117 Peripheral neuropathy HSDN C1963087 Constipation adverse event C0039590 Testicular neoplasms HSDN C0027497 Queasy C0020544 Renal hypertension HSDN C1963184 Nystagmus adverse event C3280965 Congenital cataracts, hearing loss, and neurodegeneration MalaCards C4084767 Bothered by vomiting C2240374 Eosinophil count raised HSDN C1963087 Constipation adverse event C0009475 Community mental health service HSDN C0085636 Light sensitivity C0020538 Hypertensive disease HSDN C0542476 Forgetful C2931918 Transketolase defect MalaCards C1579931 Depressed - symptom C0004576 Babesiosis MalaCards C0004134 Dyssynergia C3539123 Ceroid lipofuscinosis, neuronal, 11 MalaCards|UMLS C0007859 Pain neck C0342257 Complications of diabetes mellitus HSDN C0002962 Angina C0035042 Psychology and religion HSDN C1963091 Diarrhea adverse event C0034929 Reflex HSDN C0242936 Center pain C0040765 Transsexualism HSDN C0018681 Headache, cephalalgia C0234240 Allergic; headache UMLS C0162835 Hypopigmentation C1847132 Albinism, oculocutaneous, type i, temperature-sensitive MalaCards|HPO C1963281 Vomiting adverse event C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0917816 Deficiency mental C1864871 Chromosome 17q21.31 deletion syndrome OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0042830 Perception visual HSDN C0016927 Gag reflex C0006112 Brain diseases, metabolic HSDN C0013604 Edematous C0018235 Aggrieved HSDN C1963091 Diarrhea adverse event C0001314 Acute disease HSDN C0013604 Edematous C0023976 Long qt syndrome HSDN C0518090 Frequency of pain question C0032897 Prader-willi syndrome HSDN C0040822 D tremors C0752160 Hemangioma, cavernous, central nervous system HSDN C0455988 Hydrops fetalis non immune C1704423 Milroy disease MalaCards|HPO C1549543 Administration method - pain C2827407 Infectious otitis media HSDN C1963281 Vomiting adverse event C1845892 Hprt deficiency, neurologic variant HPO C0008031 Pain chest C0039538 Teratoma HSDN C2984058 Have pain C1253943 Fluid in the chest HSDN C0042963 Symptoms vomiting C3463824 Myelodysplastic syndrome HSDN C0036572 Convulsion C0023904 Liver neoplasms, experimental HSDN C0518090 Frequency of pain question C0042580 Vesico-ureteral reflux HSDN C1384666 Decreased hearing C0265961 Erythrokeratodermia variabilis HPO C0002965 Crescendo angina C0014170 Endometrial neoplasms HSDN C0008031 Pain chest C0003492 Aortic coarctation HSDN C0005779 Clotting C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0030193 Sense of pain C0700201 Dyssomnias HSDN C0152459 Striae C0005604 Trauma birth HSDN C0424755 Fever symptoms C0687720 Central diabetes insipidus OrphaNet|MalaCards C0026838 Spasticity muscle C2931667 Fitzsimmons walson mellor syndrome MalaCards C0007859 Pain neck C0025289 Meningitis UMLS C0037036 Increased salivation C1846058 Lubs x-linked mental retardation syndrome HPO C0020580 Decreased sensation C0085136 Central nervous system neoplasms HSDN C0015970 Fever unknown origin C0030491 Parapsoriasis HSDN C1962972 Proteinuria adverse event C0020621 Hypokalemia HSDN C1557397 Adverse event associated with pain C0149520 Acute cholecystitis HSDN C0011570 Monopolar depression C3665349 Secondary hypothyroidism OrphaNet C4085661 Usual severity nausea C0023903 Liver neoplasms HSDN C1557397 Adverse event associated with pain C0010701 Phyllodes tumor HSDN C0557874 Global developmental delay C1837884 Larsen-like syndrome MalaCards C0857305 Thrombocytopenia purpura C2937287 Hematolysis HSDN C1557397 Adverse event associated with pain C0006110 Brain death HSDN C0009398 Color vision defects C1999266 Depression adverse event HSDN C0010200 Cough symptom C0027092 Myopia HSDN C0221232 Welts C1290048 Urticaria perstans UMLS C0015970 Fever unknown origin C0033975 Psychotic disorders HSDN C4084725 Usual severity cough C1535939 Pneumocystis jiroveci pneumonia HSDN C4085210 Usual severity pain C0041428 Twin siamese HSDN C0043094 Weight gain C0005944 Metabolic bone disorder HSDN C0036572 Convulsion C1876175 Ataxia-telangiectasia variant MalaCards|HPO C1557397 Adverse event associated with pain C0022610 Kernicterus HSDN C4042891 Sleep wake disorders C0559260 Congenital scoliosis HSDN C3887638 Failure to thrive in infant C0268374 Adult junctional epidermolysis bullosa (disorder) OrphaNet|MalaCards C0042963 Symptoms vomiting C0494039 Gastrointestinal tularaemia MalaCards C1999266 Depression adverse event C2932715 Pseudohypoparathyroidism type 1b MalaCards|HPO C2203646 Jaundice C0021831 Intestinal diseases HSDN C3274924 Have been coughing C0206141 Idiopathic hypereosinophilic syndrome HSDN C0242936 Center pain C1961100 Erectile dysfunction adverse event HSDN C2024878 Cardiovascular surgery result: dyspnea C1579931 Depressed - symptom HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C4049644 Depression HSDN C4084773 Bothered by weight gain C0079744 Diffuse large b-cell lymphoma HSDN C0036572 Convulsion C0022661 Kidney failure, chronic UMLS C2364111 Gustatory anesthesia C0008728 Churg-strauss syndrome HSDN C0917816 Deficiency mental C3808184 Mental retardation, autosomal dominant 22 MalaCards C1963274 Vasculitis adverse event C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C4085210 Usual severity pain C0023798 Lipoma HSDN C1557397 Adverse event associated with pain C0030977 Perceptual masking HSDN C0020458 Hyperhydrosis C3276706 Small fiber neuropathy MalaCards C1963281 Vomiting adverse event C0740392 Infarction, middle cerebral artery HSDN C0033790 Pseudobulbar palsy C0740392 Infarction, middle cerebral artery HSDN C0018681 Headache, cephalalgia C0043528 Zoonoses HSDN C2169806 Tic C1839130 Dystonia 3, torsion, x-linked HSDN C4084788 Have dizziness C0022116 Ischemia HSDN C1279888 Proteinuria of undiagnosed cause C0032344 Poisoning aspects HSDN C3463815 Feel fatigue C0001622 Adrenal gland hyperfunction OrphaNet C1549543 Administration method - pain C0751967 Multiple sclerosis, relapsing-remitting HSDN C0700590 Diaphoresis excessive C1861457 Progressive encephalomyelitis with rigidity MalaCards C3665347 Vision impaired C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C3815497 Cough C0035956 Rupture spontaneous HSDN C0027796 Neuralgias C0011853 Diabetes mellitus, experimental HSDN C1549543 Administration method - pain C2984302 Leishmaniasis infection pathway HSDN C0003079 Pupillary inequality C0751878 Vasculitis, central nervous system HSDN C0042571 Vertigo subjective C0155523 Disorders of the vestibular system and vertiginous syndromes UMLS C0039239 Tachycardia sinus C0011633 Dermatomyositis MalaCards C0009421 Comatose C0024586 Malignant carcinoid syndrome HSDN C0043094 Weight gain C0305062 Tetanus toxoids HSDN C2984058 Have pain C3249881 Infection - suppurative HSDN C4084769 Vomiting frequency C0238386 Cronkhite-canada disease MalaCards C0015469 Facial paralysis C2911643 Encounter due to family history of osteoporosis HSDN C3463815 Feel fatigue C0042018 Urinary calculi HSDN C3898969 Have been vomiting C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C4085210 Usual severity pain C0014013 Empyema, pleural HSDN C0018772 Deafness C1963266 Uveitis adverse event HSDN C0036572 Convulsion C0023264 Leigh disease OrphaNet|HSDN|UMLS|HPO|MalaCards C4020887 Photodysphoria C3887525 Keratosis follicularis spinulosa decalvans, x-linked MalaCards C3539892 Pelvic pain in front C0001580 Adolescent behavior HSDN C0004134 Dyssynergia C1969029 Lissencephaly 3 MalaCards|HPO|UMLS C3829611 Nausea frequency C1269683 Major depressive disorder HSDN C0042798 Vision dim C0268263 Multiple sulfatase deficiency disease OrphaNet|HPO|MalaCards C0013395 Indigestion C3887532 Ulceration HSDN C0518090 Frequency of pain question C0032302 Mycoplasma pneumonia HSDN C0009806 Constipate C0033247 Proctocolitis HSDN C1549543 Administration method - pain C0011630 Dermatomycoses HSDN C1963063 Anorexia adverse event C0997768 Glaucoma HSDN C0042571 Vertigo subjective C0023448 Lymphoid leukemia HSDN C0011991 Loose stools C0004352 Autistic disorder HSDN C4084769 Vomiting frequency C0341480 Pancreas, cyst, congenital MalaCards C3887638 Failure to thrive in infant C0038644 Sudden infant death syndrome HSDN C0002962 Angina C1548484 Rheumatic fever vaccine HSDN C0727671 Red cross toothache drops C0020538 Hypertensive disease HSDN C0700590 Diaphoresis excessive C0746158 Lung lll pneumonia UMLS C0263629 Tumor-like lesions of the skin C0259771 Steatocystoma multiplex UMLS C0036396 Sciatica C0020564 Hypertrophy HSDN C4085210 Usual severity pain C0042267 Vaginitis HSDN C3463815 Feel fatigue C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse MalaCards C0557874 Global developmental delay C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C0086565 Liver function abnormal C0398691 Hyperimmunoglobulinemia d MalaCards C0085636 Light sensitivity C0085859 Polyglandular type i autoimmune syndrome OrphaNet|HPO C0002170 Alopecia disorders C2698658 Orofaciodigital syndrome type 1 MalaCards C3665492 Pigmentations C0750974 Brain tumor, primary MalaCards C4084769 Vomiting frequency C1705812 Nci thesaurus role HSDN C0917816 Deficiency mental C0032897 Prader-willi syndrome OrphaNet|MalaCards C4084768 Usual severity vomiting C0273058 Traumatic intracranial hemorrhage HSDN C3887873 Hearing loss C0021359 Infertility HSDN C4085211 Pain distress question C0007856 Cervical rib syndrome HSDN C0413252 Hypothermia due to exposure C0003615 Appendicitis HSDN C4084774 Have weight loss C0206081 Hyperandrogenism HSDN C0018772 Deafness C0796070 Microphthalmia, syndromic 7 MalaCards|HPO C0085636 Light sensitivity C1852542 Cdo syndrome MalaCards C0019214 Hepatosplenomegaly C1856306 Gsd iv, neuromuscular form, adult, with isolated myopathy HPO C1950154 Insomnia homeopathic medication C3697269 15q24 microdeletion HPO C4084769 Vomiting frequency C0019202 Hepatolenticular degeneration HSDN C0010200 Cough symptom C1708954 Mediastinal germ cell tumor with somatic-type malignancy UMLS C2911645 Weight loss adverse event C0006145 Breast diseases HSDN C0426579 Anorexia symptom C4049644 Depression HSDN C0751840 Pure alexia C0338451 Frontotemporal dementia HSDN C1963071 Back pain adverse event C1704212 Embolism embolus HSDN C4084723 Constipation C0024198 Lyme disease HSDN C4084775 Usual severity weight loss C2609414 Acute kidney injury HSDN C0031911 Pigment deposition C0242383 Age related macular degeneration MalaCards C0878773 Bladder hyperactive C0428953 Ecg infarction myocardial HSDN C0030552 Paralysis partial C0027814 Neuritis, autoimmune, experimental HSDN C0031256 Petechia C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0018991 Paralysis one side of body C0302892 Congenital porencephaly HSDN C2032395 Pelvic pain on the left C0272414 Displaced spleen HSDN C3815497 Cough C2239176 Liver carcinoma HSDN C0013604 Edematous C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084723 Constipation C3463824 Myelodysplastic syndrome HSDN C1963091 Diarrhea adverse event C0029422 Osteochondrodysplasias HSDN C3641756 Have diarrhea C0030922 Peptic ulcer hemorrhage HSDN C0020578 Hyperventilate C0027859 Acoustic neuroma HSDN C0036659 Sensation disorder C0007222 Cardiovascular diseases HSDN C0036659 Sensation disorder C0037369 Smoking HSDN C4085211 Pain distress question C0036205 Sarcoidosis, pulmonary HSDN C0349588 Stature short C0432243 Spondyloepimetaphyseal dysplasia with joint laxity OrphaNet|HPO|MalaCards C0424755 Fever symptoms C0162671 Melas syndrome MalaCards|HPO C0018926 Emesis bloody C0023518 Leukocytosis HSDN C0007758 Cerebellar ataxia C0022658 Kidney diseases HSDN C0020673 Hypothermia (central) (local) C0039841 Thiamine deficiency HSDN C1963090 Dehydration adverse event C1536500 Deficiency of acetyl-coa acetyltransferase MalaCards|HPO C1963064 Anxiety adverse event C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0003862 Pain joint C0282550 Persian gulf syndrome HSDN C0012833 Dizzy C0393534 Paraneoplastic cerebellar degeneration HSDN C4084767 Bothered by vomiting C1527348 Brain hypoxia HSDN C0042928 Paralysis vocal cord C0079541 Holoprosencephaly HSDN C4084784 Diarrhea C0010823 Cytomegalovirus infections HSDN C0427055 Face weakness C1847759 Muscular dystrophy, congenital, 1c MalaCards|HPO|UMLS C4085317 Diarrhea frequency C0021933 Intussusception HSDN C1836296 Lower extremity weakness C2675528 Spastic paraplegia 42, autosomal dominant MalaCards|UMLS C0349588 Stature short C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C1963091 Diarrhea adverse event C0341299 Collagenous sprue HSDN C3815497 Cough C0013274 Patent ductus arteriosus HSDN C0751837 Gait ataxic C0751877 Hereditary central nervous system demyelinating diseases HSDN C0234428 Consciousness disturbance C0917890 Pineocytoma MalaCards C1963167 Memory impairment adverse event C0085209 Bovine spongiform encephalitis MalaCards C0020672 Body temperature decreased C0010356 Cross infection HSDN C3815497 Cough C0017160 Gastroenteritis HSDN C0522224 Palsied C0553604 Myotonic disorders HSDN C1549543 Administration method - pain C3203360 Suppuration HSDN C3463815 Feel fatigue C1837915 Erythrocytosis, familial, 2 MalaCards|HPO C4085211 Pain distress question C0023443 Hairy cell leukemia HSDN C0019209 Large liver C0011859 Lipoatrophic diabetes mellitus OrphaNet|HPO C0036572 Convulsion C0039730 Thalassemia HSDN C4084776 Weight loss C3489413 Lipomatosis, multiple HSDN C0518090 Frequency of pain question C0024894 Mastitis HSDN C0413252 Hypothermia due to exposure C0025521 Inborn errors of metabolism HSDN C0557874 Global developmental delay C1856059 Mthfr deficiency, thermolabile type HPO C3887873 Hearing loss C0008928 Cleidocranial dysplasia HSDN C0013378 Dysgensia C0242891 Injuries teeth HSDN C0036572 Convulsion C0085096 Peripheral vascular diseases HSDN C4084775 Usual severity weight loss C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0751837 Gait ataxic C1860315 Whispering dysphonia, hereditary MalaCards C0020673 Hypothermia (central) (local) C0024117 Chronic obstructive airway disease HSDN C0009792 Consciousness disorder C1540912 Hypereosinophilic syndrome HSDN C0857305 Thrombocytopenia purpura C0011609 Drug eruptions HSDN C0013421 Dystonia C0677607 Hashimoto disease HSDN C0003467 Angst C3495554 Homocarnosinase deficiency MalaCards C1557397 Adverse event associated with pain C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C4085862 Bothered by nausea C0033923 Psychomotor function HSDN C2911645 Weight loss adverse event C0003850 Arteriosclerosis HSDN C0037763 Spasm C0342731 Deficiency of mevalonate kinase HSDN C0038868 Supranuclear palsy progressive C0032787 Postoperative complications HSDN C0015672 Decreased energy C0271934 Congenital dyserythropoietic anemia, type iii OrphaNet C0018784 Deafness sensorineural C0019294 Hernia, inguinal HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0006118 Brain neoplasms HSDN C0011991 Loose stools C2936917 Infantile polyarteritis MalaCards C1971624 Appetite absent C0276386 Mosquito-borne viral fever, oropouche MalaCards C4085641 Level of joint pain C0376300 Dengue shock syndrome MalaCards C0031256 Petechia C1842704 Gaucher disease, perinatal lethal MalaCards|HPO C3887873 Hearing loss C1306577 Dies patient HSDN C0036572 Convulsion C0009062 Clostridia infection HSDN C0085128 Cardiac output elevated C0162557 Liver failure, acute HSDN C0518090 Frequency of pain question C0016412 Folic acid deficiency HSDN C0750426 Wbc elevated C0342731 Deficiency of mevalonate kinase MalaCards C0848203 Male pelvic pain C0000768 Congenital abnormality HSDN C2984057 Have nausea C0011265 Presenile dementia HSDN C0020673 Hypothermia (central) (local) C1449861 Micronuclei, chromosome-defective HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0006145 Breast diseases HSDN C3539020 Pelvic pain decreasing in frequency C0023890 Liver cirrhosis HSDN C1963252 Tremor adverse event C0919267 Ovarian neoplasm HSDN C2315100 Pediatric failure to thrive C0020437 Hypercalcemia HSDN C2984058 Have pain C0036349 Paranoid schizophrenia HSDN C3274924 Have been coughing C0162820 Dermatitis, allergic contact HSDN C0033774 Skin pruritus C0795623 Hepatitis a vaccine, inactivated HSDN C4084727 Cough frequency C1304456 Congo hemorrhagic fever MalaCards C4084723 Constipation C3276706 Small fiber neuropathy MalaCards C0424755 Fever symptoms C3489795 Hyper-ige recurrent infection syndrome, autosomal dominant HPO C0013390 Cramps menstrual C0032787 Postoperative complications HSDN C0027498 Nausea vomiting C0024198 Lyme disease MalaCards C0004604 Pain back C0042769 Virus diseases HSDN C3641755 Have constipation C0152099 Postcholecystectomy syndrome HSDN C3887638 Failure to thrive in infant C1864723 Pyridoxamine 5-prime-phosphate oxidase deficiency HPO C2911647 Weight gain adverse event C0009395 Color perception HSDN C0026838 Spasticity muscle C0036946 Sheep--diseases HSDN C0009806 Constipate C2931294 Wiedemann grosse dibbern syndrome MalaCards C0018991 Paralysis one side of body C0007570 Celiac disease HSDN C0497247 Blood pressure elevation C0342749 Glycogen storage disease ic MalaCards|HPO C0086437 Joint hypermobility C0268345 Ehlers-danlos syndrome, arthrochalasia type HPO C0040264 Ear ringing sound C0002395 Alzheimer's disease HSDN C0460137 Push down or depress C3160718 Parkinson disease, late-onset MalaCards|HPO C4085661 Usual severity nausea C0033860 Psoriasis HSDN C0043144 Wheeze C1319018 Asthmatic bronchitis UMLS C0038506 Stutter C0236792 Asperger syndrome HSDN C3463815 Feel fatigue C0030305 Pancreatitis HSDN C0030193 Sense of pain C0039971 Thirst HSDN C0557874 Global developmental delay C2931745 Ladda zonana ramer syndrome OrphaNet|MalaCards C1963281 Vomiting adverse event C0022593 Keratosis HSDN C1963086 Confusion adverse event C0017181 Gastrointestinal hemorrhage HSDN C0010200 Cough symptom C0013291 Duodenal neoplasms HSDN C0012833 Dizzy C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0851578 Disorder sleep C0029342 Orthomyxoviridae infections HSDN C1961131 Cough adverse event C0314657 Genetic predisposition HSDN C0242936 Center pain C0600518 Choroidal neovascularization HSDN C0022638 Ketosis C0011854 Diabetes mellitus, insulin-dependent MalaCards C0018772 Deafness C0221060 Mobius syndrome MalaCards|HPO C4085642 Level of joint stiffness C2936791 Antley-bixler syndrome, autosomal dominant OrphaNet|HPO|MalaCards C0242936 Center pain C0344423 Atrial flutter by ecg finding HSDN C2315100 Pediatric failure to thrive C0268490 Tyrosinemia, type i MalaCards C0003862 Pain joint C0041327 Tuberculosis, pulmonary HSDN C0007859 Pain neck C0009450 Disease caused by microorganism HSDN C0043068 Friderichsen-waterhouse syndrome C0023364 Leptospirosis HSDN C0042025 Urinary incontinence stress C0037926 Compression of spinal cord HSDN C0018524 Hallucinate C0009088 Cluster headache HSDN C1557397 Adverse event associated with pain C0003868 Arthritis, gouty HSDN C0038002 Spleen enlargement C2673377 Mucolipidosis ii alpha/beta (disorder) HPO C0030552 Paralysis partial C0023241 Legionnaires' disease MalaCards C0700078 Deep tendon reflex decrease C3810326 Spinocerebellar ataxia, autosomal recessive 15 MalaCards C0020578 Hyperventilate C0011854 Diabetes mellitus, insulin-dependent HSDN C3665386 Abnormal vision C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0086565 Liver function abnormal C2931002 Congenital disorder of glycosylation type 1h MalaCards C4085548 Usual severity dizziness C0036690 Septicemia HSDN C0557874 Global developmental delay C3489726 Geleophysic dysplasia MalaCards C1836296 Lower extremity weakness C1864663 Hypomyelination and congenital cataract MalaCards C0042025 Urinary incontinence stress C1546533 Specimen source codes - abscess HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043065 Water electrolyte imbalance HSDN C2024893 Cardiovascular surgery result: fatigue C0042830 Perception visual HSDN C2237041 Shox gene with short stature C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0043019 Lateral medullary syndrome HSDN C1384666 Decreased hearing C1000483 Genus anemia HSDN C3665347 Vision impaired C0024437 Macular degeneration DiseaseOntology|MalaCards C0019209 Large liver C1701938 Associated pulmonary arterial hypertension OrphaNet C1963180 Neck pain adverse event C0021400 Influenza HSDN C0036659 Sensation disorder C0860603 Anxiety symptoms HSDN C4084725 Usual severity cough C1258090 Enzootic pneumonia of pigs HSDN C3463815 Feel fatigue C0013386 Dyskinesia, drug-induced HSDN C0004134 Dyssynergia C0039082 Syndrome HSDN C4085549 Dizziness C0003850 Arteriosclerosis HSDN C0162285 Edema eyelid C0020725 Type ii mucolipidosis MalaCards|HPO C1963170 Hypothermia adverse event C0236969 Substance-related disorders HSDN C1963091 Diarrhea adverse event C0032994 Pregnancy, tubal HSDN C1963137 Hydrocephalus adverse event C4014738 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 MalaCards C1549543 Administration method - pain C0027697 Nephritis HSDN C0010200 Cough symptom C1710500 Type ii pleuropulmonary blastoma UMLS C2080644 Periodic flashing lights peripherally C0085635 Photopsia UMLS C0030975 Disorders perception C0039336 Gustatory sense HSDN C0349588 Stature short C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C4084767 Bothered by vomiting C0013514 Echinostomiasis DiseaseOntology C0151311 Cranial nerve palsy C0017205 Gaucher disease MalaCards C0034155 Thrombotic thrombocytopenic purpura C0010068 Coronary heart disease HSDN C0042024 Urine incontinence C0000833 Abscess HSDN C4085317 Diarrhea frequency C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0028738 Nystagmus C2751780 Retinitis pigmentosa, juvenile, spata7-related HPO C0086437 Joint hypermobility C0878684 Short syndrome MalaCards|HPO|UMLS C0002962 Angina C0033975 Psychotic disorders HSDN C0242936 Center pain C0016436 Folliculitis HSDN C3887638 Failure to thrive in infant C0525043 Attachment disorder reactive HSDN C4084769 Vomiting frequency C0346303 Thyrotroph adenoma OrphaNet|MalaCards C1549543 Administration method - pain C0025303 Meningococcal infections HSDN C0424755 Fever symptoms C0012243 Digestive system neoplasms HSDN C0013604 Edematous C0003892 Neurogenic arthropathy HSDN C0231341 Aging premature C0027746 Nerve degeneration HSDN C4084773 Bothered by weight gain C0027121 Myositis HSDN C0242936 Center pain C1253943 Fluid in the chest HSDN C3829611 Nausea frequency C0007350 Cat disease HSDN C4084723 Constipation C0001122 Acidosis HSDN C4084775 Usual severity weight loss C0026640 Mouth neoplasms HSDN C4084776 Weight loss C0302363 Bang disease MalaCards C1963071 Back pain adverse event C0017416 Genital neoplasms, female HSDN C4085862 Bothered by nausea C0027663 Neoplasms, multiple primary HSDN C0020796 Profoundly mentally retarded C0457133 Muscle eye brain disease MalaCards C0038506 Stutter C0024141 Lupus erythematosus, systemic HSDN C3898969 Have been vomiting C0007137 Squamous cell carcinoma HSDN C0018784 Deafness sensorineural C0003850 Arteriosclerosis HSDN C0023012 Delay language C4014283 Cortical dysplasia, complex, with other brain malformations 6 MalaCards C0018524 Hallucinate C1621920 Intermediate maple syrup urine disease HPO C0011991 Loose stools C0342257 Complications of diabetes mellitus HSDN C0039870 Leanness C0038187 Starvation HSDN C0015672 Decreased energy C0016171 Fistula of intestine, excluding rectum and anus HSDN C4084802 Usual severity diarrhea C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C3641756 Have diarrhea C1858592 Carney triad OrphaNet|MalaCards C1145670 Failure respiratory C0025237 Melnick-needles syndrome MalaCards C0033774 Skin pruritus C0001430 Adenoma HSDN C1557397 Adverse event associated with pain C0036117 Salmonella infections HSDN C0030193 Sense of pain C0031315 Phantom limb pain UMLS C3829611 Nausea frequency C2937358 Cerebral hemorrhage HSDN C2203646 Jaundice C0018800 Cardiomegaly HSDN C0013604 Edematous C1801959 Histiocytic medullary reticulosis (disorder) MalaCards C0009806 Constipate C0268328 Porphobilinogen synthase deficiency MalaCards C3539893 Pelvic pain occurs with intercourse C0037313 Sleep HSDN C0018772 Deafness C0041324 Tuberculosis, osteoarticular HSDN C3463815 Feel fatigue C0271270 Oculovestibuloauditory syndrome DiseaseOntology|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0019693 Hiv infections HSDN C0026838 Spasticity muscle C3713418 Ppm-x syndrome MalaCards C0030975 Disorders perception C0751072 Frontotemporal lobar degeneration HSDN C0004604 Pain back C0035309 Retinal diseases HSDN C0007758 Cerebellar ataxia C0020550 Hyperthyroidism HSDN C0011991 Loose stools C0024810 Marijuana smoking HSDN C0151311 Cranial nerve palsy C0346303 Thyrotroph adenoma MalaCards C0018989 Paresis of one side of body C0375206 Hemiplegia and hemiparesis UMLS C4084773 Bothered by weight gain C1546847 Entity name part type - family HSDN C0004093 Asthenia C0032533 Polymyalgia rheumatica HSDN C0013604 Edematous C0013182 Drug allergy HSDN C0033774 Skin pruritus C0024525 Malacoplakia MalaCards C0575081 Abnormal gait C0268226 Type i mucolipidosis OrphaNet|HPO C0085631 Abnormal excitement C0011854 Diabetes mellitus, insulin-dependent HSDN C4084802 Usual severity diarrhea C0013289 Duodenal diseases HSDN C2919142 Short stature adverse event C2745953 Spondylometaphyseal dysplasia with dentinogenesis imperfecta OrphaNet C4084775 Usual severity weight loss C0006277 Bronchitis HSDN C0151786 Weakness muscle C0162672 Merrf syndrome MalaCards|HSDN|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0032965 Pregnancy complications, infectious HSDN C0020538 Hbp C0032001 Pituitary apoplexy OrphaNet|MalaCards C0162298 Stiffness joints C0026709 Mucopolysaccharidosis vi OrphaNet|UMLS|HPO|MalaCards C2911645 Weight loss adverse event C0035066 Renal artery obstruction HSDN C4085549 Dizziness C0038019 Spondylosis HSDN C3829611 Nausea frequency C0078981 Arachnoid cysts HSDN C3665347 Vision impaired C1423873 Cone-rod dystrophy 9 MalaCards|HPO C0039070 Collapse fleeting C0014170 Endometrial neoplasms HSDN C0036572 Convulsion C0039263 Takayasu arteritis OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C4281086 Intractable abdominal migraine UMLS C0018681 Headache, cephalalgia C0013922 Embolism HSDN C1962972 Proteinuria adverse event C0007273 Carotid artery diseases HSDN C0015672 Decreased energy C0017921 Glycogen storage disease type ii HSDN C0026884 Muteness C0243010 Viral encephalitis HSDN C4084723 Constipation C0007194 Hypertrophic cardiomyopathy HSDN C2984057 Have nausea C0085096 Peripheral vascular diseases HSDN C0424755 Fever symptoms C0019104 Hemorrhagic fevers, viral OrphaNet|HSDN|MalaCards C0023530 Leukopenia C1855109 Methylmalonic aciduria cbla type HPO C0006370 Bulimia C0000833 Abscess HSDN C4084774 Have weight loss C0024788 Green monkey virus disease OrphaNet|MalaCards C0036572 Convulsion C0282577 Congenital disorders of glycosylation OrphaNet|HSDN|MalaCards C0036659 Sensation disorder C0019693 Hiv infections HSDN C1963281 Vomiting adverse event C0010417 Cryptorchidism HSDN C0027497 Queasy C0024841 Matrimony, matrimonial HSDN C2024878 Cardiovascular surgery result: dyspnea C1843418 Niemann-pick disease, type f HPO C0018681 Headache, cephalalgia C0339959 Pneumonia chlamydial MalaCards C3163620 Hypotension adverse event C3714602 Staphylococcal toxic shock syndrome MalaCards C0002622 Amnesias C0023667 Detection, lie HSDN C2242996 Tingling C0011853 Diabetes mellitus, experimental HSDN C0349588 Stature short C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C2984058 Have pain C0042024 Urinary incontinence HSDN C0009806 Constipate C1836544 Schindler disease, type i MalaCards C0040264 Ear ringing sound C0314657 Genetic predisposition HSDN C0039239 Tachycardia sinus C0334419 Pheochromocytoma, malignant MalaCards C3887638 Failure to thrive in infant C0948187 Tracheomalacia HSDN C0010200 Cough symptom C0585442 Osteosarcoma of bone HSDN C1963249 Tinnitus adverse event C0026780 Mumps HSDN C4084802 Usual severity diarrhea C0009326 Collagen diseases HSDN C0700078 Deep tendon reflex decrease C3281192 Infantile cerebellar-retinal degeneration MalaCards C0041834 Erythematous condition C0406645 Amyopathic dermatomyositis MalaCards C3898969 Have been vomiting C0021368 Inflammation HSDN C1963281 Vomiting adverse event C0037926 Compression of spinal cord HSDN C0043068 Friderichsen-waterhouse syndrome C0040560 Toxoplasmosis, congenital HSDN C0007166 Cardiac output decreased C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0002962 Angina C1956257 Pulmonary stenosis HSDN C0009676 Confusion state C0034929 Reflex HSDN C3541349 Syncope C0162526 Aids-related opportunistic infections HSDN C0019825 Voice hoarseness C1708653 Laryngeal lymphoepithelial carcinoma UMLS C0030232 Color loss C0086774 Cold hemoglobinuria MalaCards C0221263 Cafe au lait spot C0700208 Acquired scoliosis HSDN C0038506 Stutter C0236969 Substance-related disorders HSDN C2096293 Ent surgical result ear vertigo C0014836 Escherichia coli infections HSDN C0039070 Collapse fleeting C0008626 Congenital chromosomal disease HSDN C4085222 Nausea C0038013 Ankylosing spondylitis HSDN C3887638 Failure to thrive in infant C2751630 Dursun syndrome HPO C3665346 Loss sight C0242383 Age related macular degeneration MalaCards C4084724 Usual severity constipation C0004352 Autistic disorder HSDN C0016382 Cutaneous vascular engorgement C0025323 Menorrhagia HSDN C0042420 Vasovagal episode C0013363 Dysautonomia HSDN C0007758 Cerebellar ataxia C0854723 Retinal dystrophies HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036601 Self mutilation HSDN C0036572 Convulsion C1318558 Congenital melanocytic nevus HPO C4084768 Usual severity vomiting C0002991 Cutaneous fibrous histiocytoma HSDN C1279888 Proteinuria of undiagnosed cause C0024115 Lung diseases HSDN C3539020 Pelvic pain decreasing in frequency C0017181 Gastrointestinal hemorrhage HSDN C3898969 Have been vomiting C0268621 Hepatic methionine adenosyltransferase deficiency MalaCards C4085549 Dizziness C0022876 Premature obstetric labor HSDN C3463815 Feel fatigue C0751799 Brain hemorrhage, traumatic HSDN C0018681 Headache, cephalalgia C0280381 Lymphoepithelioma of the nasopharynx, stage ii UMLS C2073625 X-ray of chest: pleural effusion C1510415 Osteosclerotic myeloma MalaCards C0011570 Monopolar depression C0751254 Creutzfeldt-jakob disease, familial MalaCards|HPO C0413252 Hypothermia due to exposure C2711227 Steatohepatitis HSDN C0023012 Delay language C1968551 Mental retardation, x-linked 79 MalaCards|HPO C1145670 Failure respiratory C2930957 Hantavirosis OrphaNet|MalaCards C0518090 Frequency of pain question C0014547 Epilepsies, partial HSDN C3146279 Coma C0003469 Anxiety disorders HSDN C0851578 Disorder sleep C0035436 Rheumatic fever HSDN C0221166 Paraparesis C0020621 Hypokalemia HSDN C2024878 Cardiovascular surgery result: dyspnea C0024081 Angina, ludwig HSDN C2911645 Weight loss adverse event C0018790 Cardiac arrest HSDN C0012833 Dizzy C3714509 Nutrition disorders HSDN C1000483 Genus anemia C0031269 Peutz-jeghers syndrome MalaCards|HPO C0151908 Dry skin C0432246 Microcephalic osteodysplastic primordial dwarfism, type ii OrphaNet|HPO C4085549 Dizziness C0032285 Pneumonia HSDN C1961131 Cough adverse event C0032533 Polymyalgia rheumatica MalaCards C4084802 Usual severity diarrhea C0026691 Mucocutaneous lymph node syndrome OrphaNet|HSDN|MalaCards C0234132 Pyramidal sign C1844933 Spinocerebellar ataxia, x-linked 4 MalaCards C1279888 Proteinuria of undiagnosed cause C1258104 Diffuse scleroderma HSDN C0004604 Pain back C0018800 Cardiomegaly HSDN C4085210 Usual severity pain C0038536 Subcutaneous emphysema HSDN C0040264 Ear ringing sound C0011854 Diabetes mellitus, insulin-dependent HSDN C4084775 Usual severity weight loss C1962976 Ventricular fibrillation adverse event HSDN C0751495 Seizure focal C4275141 Adolescent benign focal crisis UMLS C0022408 Disorder joint C1864186 Cdags syndrome MalaCards C0023380 Lethargy C0001327 Laryngitis acute HSDN C1963281 Vomiting adverse event C0006145 Breast diseases HSDN C0042963 Symptoms vomiting C0040336 Tobacco use disorder HSDN C0011991 Loose stools C0347555 Friction blister HSDN C1836296 Lower extremity weakness C1970009 Spastic paraplegia 32, autosomal recessive MalaCards|UMLS C2237041 Shox gene with short stature C1846545 Autoimmune lymphoproliferative syndrome type 2b HPO C0270948 Neurogenic muscular atrophy C1834304 Amyotrophy, hereditary neuralgic MalaCards|HPO C3463815 Feel fatigue C0878675 Erdheim-chester disease OrphaNet|HSDN|MalaCards C1963170 Hypothermia adverse event C0016470 Food allergy HSDN C2984057 Have nausea C0007125 Carcinoma, ehrlich tumor HSDN C0007398 Catatonic C0042847 Vitamin b 12 deficiency HSDN C4084769 Vomiting frequency C2748608 Lead poisoning, susceptibility to HPO C0917816 Deficiency mental C3665333 Keratitis-ichthyosis-deafness syndrome MalaCards|HPO C4085549 Dizziness C0037397 Behavior social HSDN C0020615 Hypoglycemia nos C0345904 Malignant neoplasm of liver MalaCards C0242936 Center pain C0014848 Esophageal achalasia HSDN C4084727 Cough frequency C0041296 Tuberculosis OrphaNet|HPO C0233763 Hallucinations visual C2675191 Polymicrogyria, bilateral occipital HPO C4085317 Diarrhea frequency C1416865 Lipa gene HPO C3665492 Pigmentations C0279763 Adenoacanthoma of the uterus MalaCards C0013604 Edematous C0019625 Sinus histiocytosis HSDN C0011168 Disorder deglutition C1850363 Niemann-pick disease, nova scotian type HPO C0001825 Agraphia C0027651 Tumor HSDN C0007758 Cerebellar ataxia C0270851 Benign neonatal epilepsy HSDN C0011168 Disorder deglutition C0473572 Diffuse palmoplantar keratoderma with esophageal cancer MalaCards C0085593 Chill C0035053 Spontaneous remission HSDN C4085317 Diarrhea frequency C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C0000737 Abdomen pain C0206062 Lung diseases, interstitial HSDN C0242936 Center pain C0556482 Protection sex HSDN C0221166 Paraparesis C0014009 Empyema HSDN C1549543 Administration method - pain C0019101 Hemorrhagic fever with renal syndrome HSDN C2237041 Shox gene with short stature C0162361 Hidrotic ectodermal dysplasia OrphaNet|HPO C4084768 Usual severity vomiting C0029118 Opportunistic infections HSDN C3163620 Hypotension adverse event C0242343 Panhypopituitarism OrphaNet|HPO|MalaCards C3887638 Failure to thrive in infant C0265241 Franceschetti-klein syndrome MalaCards|HPO C0028738 Nystagmus C2931599 Oculocutaneous albinism type 3 OrphaNet|HPO|MalaCards C4085211 Pain distress question C0272375 Antithrombin iii deficiency HSDN C0027066 Myoclonic jerking C0030567 Parkinson disease HSDN C1963180 Neck pain adverse event C0037744 Perceptual spatial orientation HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023374 Lesch-nyhan syndrome HSDN C0015672 Decreased energy C0221406 Pituitary-dependent cushing's disease OrphaNet|HPO C0015230 Exanthem C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C0007758 Cerebellar ataxia C2677590 Congenital disorder of glycosylation, type in MalaCards|HPO C4085211 Pain distress question C0436596 On examination - apathetic HSDN C0018926 Emesis bloody C0206733 Strawberry nevus of skin HSDN C0042963 Symptoms vomiting C0018817 Atrial septal defects HSDN C0000737 Abdomen pain C0024141 Lupus erythematosus, systemic HSDN C0030200 Intractable pain C0262655 Recurrent urinary tract infection HSDN C2919142 Short stature adverse event C0027341 Nail-patella syndrome MalaCards|HPO C3146279 Coma C0010346 Crohn disease HSDN C2237041 Shox gene with short stature C2931685 Cantalamessa baldini ambrosi syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0206704 Carcinoma, large cell HSDN C2984058 Have pain C0040947 Trichostrongyloidiasis HSDN C4084768 Usual severity vomiting C0017658 Glomerulonephritis HSDN C4084775 Usual severity weight loss C0856761 Budd-chiari syndrome MalaCards|HPO C0036572 Convulsion C0751871 Autoimmune diseases of the nervous system HSDN C3463815 Feel fatigue C0017181 Gastrointestinal hemorrhage HSDN C1963065 Apnea adverse event C0015726 Focused anxiety HSDN C0751837 Gait ataxic C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C0007758 Cerebellar ataxia C3151343 Spinocerebellar ataxia 32 MalaCards C0241210 Speaking delay C3495483 Amish brittle hair syndrome MalaCards C0039231 Heartbeats increased C0030422 Extra-adrenal paraganglioma HPO C0424755 Fever symptoms C0013117 Dreaming HSDN C0020673 Hypothermia (central) (local) C2937421 Prostatic hyperplasia HSDN C0242936 Center pain C1510415 Osteosclerotic myeloma MalaCards C0030486 Extremity paralysis, lower C0004364 Autoimmune diseases HSDN C4084767 Bothered by vomiting C0000814 Abortion, missed HSDN C2029884 Hearing loss by exam C0524812 Intracranial hypotension HSDN C1971624 Appetite absent C2984572 Malaria pathway HSDN C4084767 Bothered by vomiting C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C0013404 Respiratory difficulty C3495559 Juvenile arthritis HSDN C0027497 Queasy C0038579 Substance abuse, intravenous HSDN C0030193 Sense of pain C0282687 Hemorrhagic fever, ebola HSDN C3541349 Syncope C0751362 Narcolepsy-cataplexy syndrome MalaCards|HPO C0040822 D tremors C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C0030552 Paralysis partial C0009917 Contracture HSDN C0040485 Wryneck C0031157 Peritonsillar abscess HSDN C3665492 Pigmentations C0751688 Malignant squamous cell neoplasm MalaCards C1519353 Skin eruption papular C1968804 Plasminogen deficiency, type i MalaCards C0557911 Feel bad C1443060 Feeling abnormal UMLS C2024878 Cardiovascular surgery result: dyspnea C0205969 Thymic carcinoma OrphaNet|MalaCards C0016199 Pain flank C0206625 Malignant mixed tumor HSDN C0030193 Sense of pain C0236969 Substance-related disorders HSDN C0011991 Loose stools C0086768 Pancreatic cholera UMLS C1963087 Constipation adverse event C1550639 Specimen type - fistula HSDN C0043094 Weight gain C0040411 Tongue neoplasms HSDN C0518090 Frequency of pain question C0036216 Sarcoma, experimental HSDN C0002170 Alopecia disorders C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C0867389 Chronic graft-versus-host disease MalaCards C2984058 Have pain C0015959 Fetomaternal bleeding HSDN C0007758 Cerebellar ataxia C1269683 Major depressive disorder HSDN C0018991 Paralysis one side of body C0026769 Multiple sclerosis HSDN C0018808 Murmur C0243026 Sepsis HSDN C1963064 Anxiety adverse event C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C0015970 Fever unknown origin C3813607 Infantile gastroesophageal reflux HSDN C3274924 Have been coughing C0018081 Gonorrhea HSDN C4084802 Usual severity diarrhea C0003504 Aortic valve insufficiency HSDN C0878773 Bladder hyperactive C0018801 Heart failure HSDN C1962972 Proteinuria adverse event C0011609 Drug eruptions HSDN C2024893 Cardiovascular surgery result: fatigue C0023364 Leptospirosis HSDN C0917816 Deficiency mental C2931673 Ceroid lipofuscinosis, neuronal 1, infantile MalaCards|HPO C0018991 Paralysis one side of body C0025292 Haemophilus meningitis HSDN C2911645 Weight loss adverse event C0007097 Carcinomas HSDN C0000727 Abdomen acute C0026785 Munchhausen syndrome HSDN C0413252 Hypothermia due to exposure C0034040 Puerperal disorders HSDN C0042963 Symptoms vomiting C0011860 Diabetes mellitus, non-insulin-dependent HSDN|UMLS C0038868 Supranuclear palsy progressive C0021943 Chromosome inversion HSDN C0005745 Blepharoptosis C0265395 Anomaly of chromosome pair ring 1 syndrome OrphaNet|MalaCards C0003469 Anxiety disorder C0220704 Shprintzen syndrome MalaCards|HPO C0034124 Pupillary disorder C0161407 Injury of abducens nerve HSDN C1963093 Dizziness adverse event C0559260 Congenital scoliosis HSDN C1557397 Adverse event associated with pain C0017412 Genital diseases, male HSDN C1963087 Constipation adverse event C0042812 Acuity visual HSDN C0004604 Pain back C2963140 Arteriovenous fistula in use with two needles HSDN C0557874 Global developmental delay C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C0020542 Pulmonary hypertension HSDN C4084773 Bothered by weight gain C0019112 Hemorrhoids HSDN C0036572 Convulsion C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0027627 Neoplasm metastasis HSDN C0030193 Sense of pain C0343265 Algodystrophy of foot UMLS C0030193 Sense of pain C0232945 Dysmenorrhea, mechanical UMLS C4085222 Nausea C1704436 Peripheral arterial diseases HSDN C0149651 Clubbing C1832940 Juvenile polyposis of stomach HPO C0011570 Monopolar depression C0085547 Phenylketonuria, maternal MalaCards|HPO C0007758 Cerebellar ataxia C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C4084768 Usual severity vomiting C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0013595 Eczematous dermatitis C3489795 Hyper-ige recurrent infection syndrome, autosomal dominant OrphaNet|HPO C4084802 Usual severity diarrhea C0026847 Spinal muscular atrophy HSDN C0031911 Pigment deposition C0278803 Adenocarcinoma of small intestine MalaCards C4085210 Usual severity pain C0376670 Pancreatitis, alcoholic HSDN C4084723 Constipation C1579931 Depressed - symptom HSDN C0454644 Delayed language development C0796222 Mental retardation, x linked 16 MalaCards|HPO C1963170 Hypothermia adverse event C0037315 Sleep apnea syndromes HSDN C0234132 Pyramidal sign C0268496 Kramer syndrome OrphaNet|MalaCards C1963063 Anorexia adverse event C0007453 Cattle disease HSDN C0000737 Abdomen pain C1707443 Colorectal undifferentiated carcinoma UMLS C0035078 Failure kidney C1855675 Arima syndrome MalaCards|HPO C0030193 Sense of pain C0040021 Thromboangiitis obliterans MalaCards C4085549 Dizziness C1704436 Peripheral arterial diseases HSDN C0030193 Sense of pain C0867389 Chronic graft-versus-host disease MalaCards C0162275 Ketoaciduria C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C2242996 Tingling C0035127 Cumulative trauma disorders HSDN C0860603 Anxiety symptom C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C0242936 Center pain C0030299 Pancreatic pseudocyst HSDN C0018681 Headache, cephalalgia C3812171 Bradycardia by ecg finding HSDN C0151818 Opisthotonos C1291386 D-glycericacidemia MalaCards|HPO C0424755 Fever symptoms C0554114 Epstein-barr virus hepatitis MalaCards C0011991 Loose stools C0031069 Familial mediterranean fever OrphaNet|HPO C0020578 Hyperventilate C0027804 Fatigue neurosis HSDN C0042024 Urine incontinence C0020437 Hypercalcemia HSDN C0023014 Developmental disorder language C0011581 Depressive disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020119 Human development HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0520720 Cyst nerve root HSDN C4085642 Level of joint stiffness C1867774 Sacral agenesis syndrome OrphaNet|HPO C0027066 Myoclonic jerking C0024141 Lupus erythematosus, systemic HSDN C0026821 Cramp C3665624 Serum calcium below normal HSDN C0232849 Bladder pain C0010692 Cystitis UMLS C4018871 Abnormality of the respiratory system C1849649 Holoprosencephaly polydactyly syndrome MalaCards C0021359 Infertility C0265498 48, xxxy syndrome OrphaNet|MalaCards C0013404 Respiratory difficulty C0024586 Malignant carcinoid syndrome HSDN C1963093 Dizziness adverse event C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards C0030193 Sense of pain C0012644 Animal disease models HSDN C0013405 Dyspnea, paroxysmal C0001883 Airway obstruction HSDN C1069915 Vertigo C0453996 Tobacco smoking HSDN C0019572 Hairiness C0018671 Head and neck neoplasms HSDN C0424755 Fever symptoms C3495801 Granulomatosis with polyangiitis OrphaNet|HSDN|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0024523 Malabsorption syndrome HSDN C1963170 Hypothermia adverse event C0014556 Epilepsy, temporal lobe HSDN C0004604 Pain back C0034088 Pulmonary valve insufficiency HSDN C0851578 Disorder sleep C0270853 Myoclonic epilepsy, juvenile HSDN C4084774 Have weight loss C0042035 Urination disorders HSDN C0042940 Disorder of voice C0751950 Neuromuscular junction diseases HSDN C0018772 Deafness C0041466 Typhoid fever HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1962976 Ventricular fibrillation adverse event HSDN C1963154 Renal failure adverse event C3715199 Renal-hepatic-pancreatic dysplasia 1 MalaCards C0009421 Comatose C0036986 Shock, traumatic HSDN C3641756 Have diarrhea C0037073 Sigmoid neoplasms HSDN C0037316 Not enough sleeping C0002395 Alzheimer's disease HSDN C0424755 Fever symptoms C0241954 Jaundice, infectious MalaCards C0013604 Edematous C0473586 Michelin tire baby syndrome OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C2586211 Thrombosis of blood vessel HSDN C0241210 Speaking delay C0265245 Nager syndrome OrphaNet|HPO|MalaCards C0028738 Nystagmus C2985219 Papillary tumor of the pineal region OrphaNet|MalaCards C0520966 Coordination impaired C0162309 Adrenoleukodystrophy OrphaNet|UMLS|HPO|MalaCards C4084766 Vomiting C0016542 Foreign body HSDN C3665347 Vision impaired C2931008 Congenital disorder of glycosylation type 2a MalaCards C2048468 Inability to impregnate C2676235 Ciliary dyskinesia, primary, 9 HPO C0015672 Decreased energy C0022660 Kidney failure, acute HSDN C0042798 Vision dim C2931074 Cone rod dystrophy amelogenesis imperfecta OrphaNet|HPO|MalaCards C1549543 Administration method - pain C1414542 Fbn1 gene HSDN C0019209 Large liver C1853136 Neutral lipid storage disease with myopathy MalaCards|HPO C0026821 Cramp C0009240 Cognition HSDN C0034150 Skin purpura C0023890 Liver cirrhosis HSDN C1963137 Hydrocephalus adverse event C1849649 Holoprosencephaly polydactyly syndrome OrphaNet|MalaCards C1549543 Administration method - pain C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C0040264 Ear ringing sound C3888210 Deafness, autosomal dominant 58 MalaCards C0018777 Deafness, conductive C0376524 Branchio-oculo-facial syndrome OrphaNet|HPO|MalaCards C4084727 Cough frequency C0004623 Bacterial infections HSDN C0019825 Voice hoarseness C0587248 Costello syndrome (disorder) MalaCards|HPO|UMLS C0018772 Deafness C2363065 Vitamin d-resistant rickets MalaCards C2188220 Unusual behavior C0424295 Hyperactive behavior UMLS C0030486 Extremity paralysis, lower C0019699 Hiv seropositivity HSDN C1579931 Depressed - symptom C1858028 Wolfram syndrome 2 HPO C0234428 Consciousness disturbance C0809994 Coma; stupor; and brain damage UMLS C4085222 Nausea C0051981 Anti-leprosy vaccine HSDN C1971624 Appetite absent C0011570 Mental depression HSDN C0520966 Coordination impaired C1970431 Pitt-hopkins syndrome MalaCards|HPO|UMLS C0006370 Bulimia C0556346 Binge drinking HSDN C0030486 Extremity paralysis, lower C0013295 Duodenal ulcer HSDN C2029884 Hearing loss by exam C0220726 Diastrophic dysplasia MalaCards C0349588 Stature short C0796200 Wieacker-wolff syndrome MalaCards C0860603 Anxiety symptom C0339534 Usher syndrome type 2 MalaCards|HPO C0013604 Edematous C0018789 Cardiac aneurysm HSDN C0476273 Distress respiratory C0006849 Oral candidiasis UMLS C0149793 Transient monocular blindness C0003857 Congenital arteriovenous malformation HSDN C0162834 Hyperpigmentation C1260961 Lipoatrophia semicircularis MalaCards C4085317 Diarrhea frequency C0012814 Colon nos diverticulitis HSDN C2911647 Weight gain adverse event C0206062 Lung diseases, interstitial HSDN C0026838 Spasticity muscle C0795841 Jacobsen distal 11q deletion syndrome MalaCards|UMLS C0038990 Sweats C1861848 Paragangliomas 4 MalaCards|HPO C4084897 Sleep disturbance subordinate domain C0334123 Histiocytosis, lipoid MalaCards C1963184 Nystagmus adverse event C0398794 Hypopigmentation-immunodeficiency disease MalaCards C4084775 Usual severity weight loss C0022876 Premature obstetric labor HSDN C0040034 Thrombocytopenia C1861185 Thrombocytopenia 2 (disorder) MalaCards|HPO C4085549 Dizziness C0013990 Pathological accumulation of air in tissues HSDN C0042025 Urinary incontinence stress C3827868 Tachycardia by ecg finding HSDN C0023015 Language handicap C0036363 Schizotypal personality disorder HSDN C0040822 D tremors C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C0004134 Dyssynergia C1848201 Subcortical band heterotopia HPO C1963091 Diarrhea adverse event C0149721 Left ventricular hypertrophy HSDN C4085317 Diarrhea frequency C1135821 Mortality syndrome, spiking HSDN C0013595 Eczematous dermatitis C0029411 Osteoarthropathy, primary hypertrophic MalaCards|HPO C0231807 Dyspnea exertional C0018802 Congestive heart failure UMLS C0497406 Over weight C0042138 Uterine neoplasms HSDN C0424810 Periorbital swelling C0007932 Chagas' disease + no organ inv MalaCards C0018991 Paralysis one side of body C0032269 Pneumococcal infections HSDN C0012833 Dizzy C4085311 Depression - recess HSDN C2315100 Pediatric failure to thrive C0342720 Adenosylcobalamin synthesis defect MalaCards C2984058 Have pain C0525045 Mood disorders HSDN C4084802 Usual severity diarrhea C0038587 Substance withdrawal syndrome HSDN C0040264 Ear ringing sound C3542996 Mindfulness HSDN C0018834 Brash C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0002963 Angina variant C0460137 Push down or depress HSDN C1549543 Administration method - pain C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C0023380 Lethargy C0011142 Defense mechanism HSDN C0518090 Frequency of pain question C0029139 Optical illusion HSDN C4085210 Usual severity pain C0027401 Narcissism HSDN C0020538 Hbp C0300948 Caudal regression syndrome HPO C0015469 Facial paralysis C1853198 Cold-induced sweating syndrome 2 HPO C3541349 Syncope C0006147 Breast fed HSDN C2242996 Tingling C0007274 Carotid artery thrombosis HSDN C1000483 Genus anemia C0263591 Lupus erythematosus drug induced MalaCards C2919142 Short stature adverse event C4015513 Myopathy, isolated mitochondrial, autosomal dominant MalaCards C4084788 Have dizziness C0018944 Hematoma HSDN C0234533 Seizure generalized C3281202 Mental retardation, autosomal dominant 13 MalaCards C3898969 Have been vomiting C0043168 Whooping cough due to unspecified organism HSDN C0011991 Loose stools C0024282 Lymphocytosis HSDN C0427055 Face weakness C0027859 Acoustic neuroma HPO C0040264 Ear ringing sound C0003864 Arthritis HSDN C3539896 Pelvic pain occurs with urination C0005491 Biofeedback HSDN C4085317 Diarrhea frequency C0025958 Microcephaly HSDN C2315100 Pediatric failure to thrive C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C2984058 Have pain C0032227 Pleural effusion disorder HSDN C0025287 Meningitis-like C0002895 Anemia, sickle cell HSDN C2911645 Weight loss adverse event C0872315 Communicable diseases emerging HSDN C0000737 Abdomen pain C0025345 Menstruation disturbances HSDN C0003862 Pain joint C1847593 Epiphyseal dysplasia, multiple, 4 OrphaNet|UMLS|HPO|MalaCards C1557397 Adverse event associated with pain C3203360 Suppuration HSDN C0036396 Sciatica C2911643 Encounter due to family history of osteoporosis HSDN C0233844 Awkwardness C0221060 Mobius syndrome MalaCards C3815497 Cough C3495801 Granulomatosis with polyangiitis OrphaNet|HSDN|HPO|MalaCards C4084774 Have weight loss C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C4085317 Diarrhea frequency C1510412 Pseudoaneurysm HSDN C0423708 Obturator neuralgia C1290837 Disease of trunk UMLS C4085317 Diarrhea frequency C3150751 Agammaglobulinemia 3, autosomal recessive HPO C2024878 Cardiovascular surgery result: dyspnea C0039978 Thoracic diseases HSDN C0013132 Drooling C0795889 Allan-herndon-dudley syndrome (ahds) MalaCards|HPO C4020887 Photodysphoria C2675066 Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus HPO C4085317 Diarrhea frequency C0020757 Ichthyoses HSDN C0410924 Underfeeding of newborn C0554614 Other perinatal conditions UMLS C4084802 Usual severity diarrhea C1835888 Diarrhea 4, malabsorptive, congenital MalaCards|HPO C4084774 Have weight loss C0006309 Brucellosis HSDN C0036572 Convulsion C0037315 Sleep apnea syndromes HSDN C1963090 Dehydration adverse event C1866495 Bartter syndrome, antenatal type 1 HPO C0040034 Thrombocytopenia C0342701 Transcobalamin ii deficiency OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C0029294 Orofaciodigital syndromes MalaCards C0518090 Frequency of pain question C0027719 Nephrosclerosis HSDN C4084775 Usual severity weight loss C0022665 Kidney neoplasm HSDN C4084767 Bothered by vomiting C0024667 Animal mammary neoplasms HSDN C0518090 Frequency of pain question C0027439 Nasopharyngeal neoplasms HSDN C4085549 Dizziness C0005695 Bladder neoplasm HSDN C4085211 Pain distress question C0034362 Q fever HSDN C0344434 Atrial fibrillation ecg C1970119 Cardiac arrhythmia, ankyrin-b-related MalaCards|HPO C0011991 Loose stools C0341299 Collagenous sprue HSDN C0242936 Center pain C0015302 External exotoses HSDN C1962972 Proteinuria adverse event C1535939 Pneumocystis jiroveci pneumonia HSDN C0271215 Blindness legal C1858991 Childhood ataxia with central nervous system hypomyelinization MalaCards|HPO C0024031 Back pain lower back C0013806 Electroplexy shock therapy HSDN C0011570 Monopolar depression C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C4084776 Weight loss C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C3898969 Have been vomiting C0016627 Avian influenza DiseaseOntology|MalaCards C2315100 Pediatric failure to thrive C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C0037036 Increased salivation C0796028 Ataxia, fatal x-linked, with deafness and loss of vision MalaCards|HPO C4085211 Pain distress question C0006264 Bronchial neoplasms HSDN C3463815 Feel fatigue C0683253 Psychological resilience HSDN C1549543 Administration method - pain C0206681 Adenocarcinoma, clear cell HSDN C0018681 Headache, cephalalgia C0025286 Meningioma MalaCards C1963170 Hypothermia adverse event C0518450 Spinal fractures HSDN C0812426 Kidney problem C0748310 Renal failure non oliguric UMLS C0013604 Edematous C0035441 Rheumatic nodule HSDN C4084775 Usual severity weight loss C0024620 Primary malignant neoplasm of liver MalaCards C0232466 Feeding difficulty C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency HPO C4084784 Diarrhea C0031046 Pericarditis HSDN C2984058 Have pain C0032463 Polycythemia vera HSDN C0042798 Vision dim C3888026 Hermansky-pudlak syndrome 8 MalaCards C1963281 Vomiting adverse event C0019066 Nontraumatic hemoperitoneum HSDN C4084726 Distress cough C0037116 Silicosis HSDN C1557397 Adverse event associated with pain C0026918 Mycobacterium infections HSDN C1557397 Adverse event associated with pain C0024449 Fungal mycetoma HSDN C1557397 Adverse event associated with pain C0919691 Anastomotic leaks HSDN C0036572 Convulsion C4053775 Pituitary stalk interruption syndrome MalaCards C0085636 Light sensitivity C3805375 Albinism, oculocutaneous, type vi MalaCards C0015469 Facial paralysis C3178801 Stroke, lacunar HSDN C0030193 Sense of pain C0012546 Diphtheria HSDN C4084784 Diarrhea C0086543 Cataract nos HSDN C4085211 Pain distress question C0020295 Hydronephrosis HSDN C1999266 Depression adverse event C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C4085210 Usual severity pain C1705811 Terminology role entity HSDN C0015672 Decreased energy C0005119 Bereavement HSDN C0025323 Bleeding menstrual heavy C0272309 Simple bruising MalaCards C0003862 Pain joint C4225334 Autoimmune interstitial lung, joint, and kidney disease UMLS C0522224 Palsied C1442903 Exostoses HSDN C0013404 Respiratory difficulty C0241158 Cicatrix skin HSDN C3898969 Have been vomiting C1857855 Spastic paraplegia 29, autosomal dominant MalaCards C0013390 Cramps menstrual C0011581 Depressive disorder HSDN C0018991 Paralysis one side of body C0013926 Aeroembolism HSDN C3641755 Have constipation C2673611 Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant HPO C4084769 Vomiting frequency C0342701 Transcobalamin ii deficiency MalaCards C4084788 Have dizziness C3827868 Tachycardia by ecg finding HSDN C0009421 Comatose C1423541 Vangl2 gene HSDN C0030486 Extremity paralysis, lower C0025299 Meningocele HSDN C1963237 Insomnia adverse event C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C1963137 Hydrocephalus adverse event C1859526 Beemer ertbruggen syndrome MalaCards C0085606 Urination urgency C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0008031 Pain chest C0679360 Foodborne disease HSDN C0035078 Failure kidney C3809320 Nephronophthisis 16 MalaCards C0427068 Legs weakness C0393559 Troyer syndrome HPO C4084726 Distress cough C0024307 Lymphomatoid granulomatosis HSDN C0424755 Fever symptoms C0014534 Epididymitis HSDN C0042798 Vision dim C2930852 Zellweger leukodystrophy MalaCards C4085222 Nausea C0011127 Pressure ulcer HSDN C0019209 Large liver C0022350 Jaundice, chronic idiopathic MalaCards|HPO C0037317 Sleep disturbance C0040517 Gilles de la tourette syndrome MalaCards|HPO|UMLS C0749830 Upper extremity pain increasing C0741096 Upper_ext problem UMLS C0030193 Sense of pain C2364172 Adherence to medication regime HSDN C4084723 Constipation C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C4084775 Usual severity weight loss C0878675 Erdheim-chester disease OrphaNet|HSDN|MalaCards C0018991 Paralysis one side of body C0702221 Tactual discrimination HSDN C4084768 Usual severity vomiting C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0030193 Sense of pain C0040336 Tobacco use disorder HSDN C1971624 Appetite absent C0023794 Lipoidosis HSDN C0030232 Color loss C0033027 Preleukemia HSDN C0027066 Myoclonic jerking C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C1963071 Back pain adverse event C0029927 Ovarian cysts HSDN C1557397 Adverse event associated with pain C0030767 Grouping peer HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0000786 Spontaneous abortion HSDN C0522224 Palsied C0029463 Osteosarcoma HSDN C4084724 Usual severity constipation C0344434 Atrial fibrillation ecg HSDN C0234132 Pyramidal sign C0022336 Creutzfeldt-jakob disease MalaCards C0026858 Musculoskeletal pain C0221204 Lytic lesion HSDN C0522224 Palsied C1548483 Leishmaniasis vaccine HSDN C3146279 Coma C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0349588 Stature short C0796202 Wittwer syndrome MalaCards C0030193 Sense of pain C2189139 Varicose veins with pain UMLS C1549543 Administration method - pain C0162832 Apc HSDN C0406403 Delayed dermographism C0042109 Urticaria UMLS C4085222 Nausea C0013595 Eczema HSDN C1279888 Proteinuria of undiagnosed cause C2939462 Immunoglobulin deposition disease MalaCards C0221232 Welts C0524988 Schnitzler syndrome UMLS C0018991 Paralysis one side of body C0021308 Infarction HSDN C0030552 Paralysis partial C0028768 Obsessive-compulsive disorder HSDN C0027497 Queasy C0003869 Arthritis, infectious HSDN C0036572 Convulsion C0016053 Fibromyalgia HSDN C0000737 Abdomen pain C0002438 Amebiasis HSDN C4085210 Usual severity pain C2936490 Cardiac arrest, out-of-hospital HSDN C2919142 Short stature adverse event C2931285 Congenital testicular deficiency MalaCards C0476250 Head neck mass C0162375 Cell central giant granulomas UMLS C0027497 Queasy C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0015672 Decreased energy C1962979 Burn adverse event HSDN C1963091 Diarrhea adverse event C0043395 Yellow fever OrphaNet|MalaCards C0030193 Sense of pain C4054114 Recurrent adult undifferentiated high grade pleomorphic sarcoma UMLS C0151786 Weakness muscle C0031212 Personality disorders HSDN C0033790 Pseudobulbar palsy C0577628 Latex allergy HSDN C2024893 Cardiovascular surgery result: fatigue C0175816 Cold hemagglutinin disease OrphaNet|MalaCards C0013390 Cramps menstrual C0014179 Endometritis HSDN C0575081 Abnormal gait C0393590 Fahr's syndrome (disorder) MalaCards|HPO C4085642 Level of joint stiffness C0599973 Waardenburg anophthalmia syndrome OrphaNet|HPO|MalaCards C0020673 Hypothermia (central) (local) C0018021 Goiter HSDN C4084788 Have dizziness C0009373 Colonic diseases HSDN C0004093 Asthenia C0002063 Alkalosis HSDN C0030193 Sense of pain C0004782 Basal ganglia diseases HSDN C3463815 Feel fatigue C0019284 Diaphragmatic hernia HSDN C0041657 Consciousness loss C0878576 Posterior leucoencephalopathy syndrome HSDN C0007758 Cerebellar ataxia C0015398 Eye diseases, hereditary HSDN C1549543 Administration method - pain C0036330 Schistosomiasis mansoni HSDN C1549543 Administration method - pain C0035459 Atrophic rhinitis HSDN C1999266 Depression adverse event C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0038868 Supranuclear palsy progressive C0043020 Wallerian degeneration HSDN C0557874 Global developmental delay C4015253 Mitochondrial complex iii deficiency, nuclear type 9 MalaCards C0040822 D tremors C0033578 Prostatic neoplasms HSDN C0026858 Musculoskeletal pain C0221002 Hyperparathyroidism, primary HSDN C0008031 Pain chest C0401151 Chronic diarrhea UMLS C0020438 Hypercalciuria C0027651 Tumor HSDN C0030554 Abnormal sensation C0034931 Reflex sympathetic dystrophy HSDN C0015469 Facial paralysis C0015456 Facial dermatoses HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0005830 Blood protein disorders HSDN C0234132 Pyramidal sign C0268540 Hhh syndrome HPO|UMLS C1963252 Tremor adverse event C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0241157 Skin pustule C3280501 Inflammatory skin and bowel disease, neonatal, 1 MalaCards C2233630 Bumpy eyelid growth C0015424 Eyelid neoplasms UMLS C0018784 Deafness sensorineural C1970187 Deafness, sensorineural, and male infertility OrphaNet|HPO|MalaCards C0002962 Angina C0243026 Sepsis HSDN C0039070 Collapse fleeting C0004096 Asthma HSDN C3815497 Cough C2931854 Allergic bronchopulmonary mycosis MalaCards C0043094 Weight gain C0042134 Uterine hemorrhage HSDN C1963281 Vomiting adverse event C0205788 Histiocytoid hemangioma HSDN C0040822 D tremors C0037036 Sialorrhea HSDN C0025287 Meningitis-like C0006105 Brain abscess HSDN C0030193 Sense of pain C0005716 Blastomycosis HSDN C0019825 Voice hoarseness C0410204 Myopathy, centronuclear, autosomal recessive HPO C0003862 Pain joint C2347126 Microscopic polyarteritis MalaCards|HSDN C0042571 Vertigo subjective C0020522 Delayed hypersensitivity HSDN C1963281 Vomiting adverse event C0717360 Disease lyme vaccine HSDN C0020673 Hypothermia (central) (local) C0035410 Rhabdomyolysis HSDN C1384666 Decreased hearing C0035934 Rubinstein-taybi syndrome MalaCards|HPO C0015300 Ocular proptosis C1860145 Acrocraniofacial dysostosis OrphaNet|MalaCards C4084724 Usual severity constipation C0238198 Gastrointestinal stromal tumors OrphaNet|HPO|MalaCards C0040264 Ear ringing sound C1136042 Neuroma, acoustic, bilateral HPO C0009792 Consciousness disorder C0026650 Movement disorders HSDN C1963091 Diarrhea adverse event C1865643 Cholestasis, progressive familial intrahepatic 3 HPO C0240715 Perineal lump C1321480 Vulval verrucous carcinoma of Buschke-Lowenstein UMLS C0033774 Skin pruritus C0585442 Osteosarcoma of bone HSDN C0518090 Frequency of pain question C0024286 Lymphogranuloma venereum HSDN C4085211 Pain distress question C0032217 Pleasure pain principle HSDN C0013421 Dystonia C4225379 Lipoyltransferase 1 deficiency UMLS C4085317 Diarrhea frequency C0042018 Urinary calculi HSDN C0022346 Yellow skin C0026865 Mushroom poisoning HSDN C0037316 Not enough sleeping C1962976 Ventricular fibrillation adverse event HSDN C4084768 Usual severity vomiting C0038454 Cerebrovascular accident HSDN C0013604 Edematous C0019326 Ventral hernia HSDN C0750426 Wbc elevated C0037054 Sickle cell trait MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1861848 Paragangliomas 4 MalaCards C0042963 Symptoms vomiting C0268412 Infantile hypophosphatasia MalaCards|HPO|UMLS C0026821 Cramp C1704436 Peripheral arterial diseases HSDN C1963184 Nystagmus adverse event C0555206 Chiari malformation type ii MalaCards C0039070 Collapse fleeting C0021655 Insulin resistance HSDN C2911645 Weight loss adverse event C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C4085549 Dizziness C0023530 Leukopenia HSDN C3539893 Pelvic pain occurs with intercourse C0221752 Rbc urine HSDN C4084802 Usual severity diarrhea C0032019 Pituitary neoplasms HSDN C0015970 Fever unknown origin C0006840 Candidiasis HSDN C0018991 Paralysis one side of body C0752160 Hemangioma, cavernous, central nervous system HSDN C1963086 Confusion adverse event C0025289 Meningitis HSDN C0011991 Loose stools C0035229 Respiratory insufficiency HSDN C0008031 Pain chest C0023092 Lassa fever OrphaNet|MalaCards C0014591 Bleeding nose C0340978 May-hegglin anomaly HPO C4084723 Constipation C0015695 Fatty liver HSDN C0042025 Urinary incontinence stress C0006145 Breast diseases HSDN C3463815 Feel fatigue C0023418 Leukemia HSDN C0030193 Sense of pain C0040441 Broken teeth HSDN C0023015 Language handicap C1969562 Mental retardation, autosomal dominant 1 HPO C0497247 Blood pressure elevation C1859565 Bardet-biedl syndrome 7 HPO C2911647 Weight gain adverse event C0011303 Demyelinating diseases HSDN C0206146 Myocardial stunning C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0027497 Queasy C1509147 Histiocytoma HSDN C0851578 Disorder sleep C0013363 Dysautonomia HSDN C0518090 Frequency of pain question C0024143 Lupus nephritis HSDN C0333240 Acute edema C0398350 Acute cardiac pulmonary edema UMLS C0018772 Deafness C0338508 Optic atrophy, autosomal dominant HSDN C1963281 Vomiting adverse event C0020522 Delayed hypersensitivity HSDN C0020673 Hypothermia (central) (local) C0042214 Vaccinia HSDN C1963086 Confusion adverse event C0022658 Kidney diseases HSDN C0040264 Ear ringing sound C0497327 Dementia HSDN C3887873 Hearing loss C2937358 Cerebral hemorrhage HSDN C4085210 Usual severity pain C0010038 Corneal opacity HSDN C2984058 Have pain C0035372 Rett syndrome HSDN C3887638 Failure to thrive in infant C3489393 Hiatal hernia HSDN C0030193 Sense of pain C0000810 Incomplete spontaneous abortion HSDN C0020672 Body temperature decreased C0007097 Carcinomas HSDN C2911647 Weight gain adverse event C0010674 Cystic fibrosis HSDN C0018784 Deafness sensorineural C0023530 Leukopenia HSDN C3463815 Feel fatigue C0011311 Dengue fever HSDN C0035232 Diaphragmatic paralysis C0268446 Thyrotoxic periodic paralysis MalaCards|HPO C2108113 Continuous electrocardiogram ventricular tachycardia C0340485 Familial ventricular tachycardia MalaCards C3203358 Alveolar hypoventilation C0013473 Eating disorders HSDN C3463815 Feel fatigue C0040100 Thymoma OrphaNet|MalaCards C1963184 Nystagmus adverse event C1865695 Spondylometaphyseal dysplasia, axial MalaCards C4085210 Usual severity pain C0027070 Myoepithelioma HSDN C2984058 Have pain C0872996 Q fever vaccine HSDN C1963180 Neck pain adverse event C0032914 Pre-eclampsia HSDN C0042798 Vision dim C1842836 Congenital disorder of glycosylation, type ii MalaCards|HPO C1069915 Vertigo C2984572 Malaria pathway HSDN C0010200 Cough symptom C0595812 Fistula route HSDN C4085642 Level of joint stiffness C2746068 Congenital idiopathic intestinal pseudoobstruction MalaCards C0026826 High muscle tone C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0162871 Aortic aneurysm, abdominal HSDN C2242996 Tingling C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084767 Bothered by vomiting C0020522 Delayed hypersensitivity HSDN C4085317 Diarrhea frequency C0005396 Bile duct neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006818 Campylobacter infection HSDN C0007166 Cardiac output decreased C2937421 Prostatic hyperplasia HSDN C4084724 Usual severity constipation C0023470 Myeloid leukemia HSDN C3815497 Cough C0262655 Recurrent urinary tract infection HSDN C3241945 Melena due to gastrointestinal hemorrhage C1838163 Osler-rendu-weber syndrome 2 MalaCards|HPO C3541349 Syncope C0031511 Pheochromocytoma HSDN C0424755 Fever symptoms C3541994 Drug hypersensitivity syndrome OrphaNet|MalaCards C4084774 Have weight loss C0018674 Head trauma HSDN C0037763 Spasm C0021308 Infarction HSDN C0034933 Abnormal reflexes C0036946 Sheep--diseases HSDN C4085210 Usual severity pain C0014474 Ependymoma HSDN C0231515 Diffuse spasm C0014863 Esophageal spasm diffuse UMLS C0007758 Cerebellar ataxia C0333641 Atrophic HSDN C0034933 Abnormal reflexes C2984289 Melanoma pathway HSDN C0030554 Abnormal sensation C0151744 Myocardial ischemia HSDN C4049644 Depression C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C0239181 Diarrhea intermittent C0268146 Glucose-6-phosphate transport defect MalaCards C0016204 Fart C0037072 Diseases sigmoid HSDN C0011991 Loose stools C0017185 Gastrointestinal neoplasms HSDN C0853986 Lymphocytes decreased C4014371 Immunodeficiency 23 MalaCards C0751837 Gait ataxic C1333598 Fap associated medulloblastoma UMLS C0018784 Deafness sensorineural C0152026 Retinal vasculitis HSDN C1963091 Diarrhea adverse event C0027430 Nasal polyps HSDN C0162834 Hyperpigmentation C0001403 Addison disease OrphaNet C2024878 Cardiovascular surgery result: dyspnea C0702094 Agranulocytosis lab result HSDN C4085862 Bothered by nausea C0008775 Ciguatera poisoning HSDN C0231528 Muscle pain generalized C4011726 Myopathy, tubular aggregate, 1 MalaCards C0023015 Language handicap C0010674 Cystic fibrosis HSDN C0028738 Nystagmus C1857351 Dandy walker malformation postaxial polydactyly MalaCards C0002965 Crescendo angina C0027686 Pathologic neovascularization HSDN C0013404 Respiratory difficulty C0026769 Multiple sclerosis HSDN C0518090 Frequency of pain question C0080233 Tooth loss HSDN C0349588 Stature short C4015436 Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus MalaCards C0917816 Deficiency mental C3887992 Thyrotropin-releasing hormone deficiency MalaCards C0151740 Intracranial hypertension C2931263 Familial cerebral cavernous malformation OrphaNet|MalaCards C3815497 Cough C0006288 Bronchopulmonary sequestration HSDN C0020615 Hypoglycemia nos C1419156 Pygl gene HPO C0036572 Convulsion C0023364 Leptospirosis HSDN C0043094 Weight gain C0016724 Froehlich's syndrome HSDN C0019209 Large liver C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C1963091 Diarrhea adverse event C0035358 Retroperitoneal neoplasm HSDN C0085606 Urination urgency C1853247 Spastic paraplegia 31, autosomal dominant MalaCards|HPO C2936821 Spinal cerebrospinal fluid leak C1861329 Spinal canal stenosis HSDN C0030193 Sense of pain C0035369 Retroviridae infections HSDN C0151889 Reflexes tendon increased C2931092 Maternally inherited leigh syndrome MalaCards C3815497 Cough C0008728 Churg-strauss syndrome MalaCards C4084802 Usual severity diarrhea C0040425 Tonsillitis HSDN C4084788 Have dizziness C1510412 Pseudoaneurysm HSDN C0575081 Abnormal gait C0029534 Other cerebellar ataxia MalaCards C0011991 Loose stools C0279727 Carcinoma, delta cell, pancreatic UMLS C0018772 Deafness C0039336 Gustatory sense HSDN C0013404 Respiratory difficulty C0007682 Cns disorder HSDN C0231341 Aging premature C0162671 Melas syndrome HSDN C0036572 Convulsion C3889476 Benign familial convulsion MalaCards C0043094 Weight gain C0878544 Cardiomyopathies HSDN C0019209 Large liver C2931895 Pericardial constriction with growth failure OrphaNet|HPO|MalaCards C4085549 Dizziness C0003125 Anorexia nervosa HSDN C2203646 Jaundice C1261473 Sarcoma HSDN C0015468 Face pain C0008090 Child reactive disorder HSDN C0011570 Monopolar depression C3149705 Parkinson disease 1, autosomal dominant lewy body HPO C4085210 Usual severity pain C3203360 Suppuration HSDN C0002962 Angina C0035204 Respiration disorders HSDN C0036572 Convulsion C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C4084802 Usual severity diarrhea C0024525 Malacoplakia MalaCards C4085222 Nausea C0013299 Duodenogastric reflux HSDN C3146279 Coma C0015927 Intrauterine fetal demise HSDN C2911647 Weight gain adverse event C0017563 Gingival diseases HSDN C0221263 Cafe au lait spot C1856796 Estren-dameshek variant of fanconi anemia HPO C3887638 Failure to thrive in infant C0152094 Cellular immunodeficiency with abnormal immunoglobulin deficiency MalaCards C0723402 Sore throat C0024788 Green monkey virus disease DiseaseOntology|MalaCards C0009806 Constipate C0795825 Chromosome 8, trisomy 8p MalaCards C0042963 Symptoms vomiting C0037928 Spinal cord diseases HSDN C0011991 Loose stools C0520773 Colitis helicobacter-associated UMLS C0008031 Pain chest C0340375 Subaortic stenosis HSDN C2911647 Weight gain adverse event C0014175 Endometriosis HSDN C0162298 Stiffness joints C4024957 Proximal spinal muscular atrophy MalaCards C0003811 Cardiac rhythm disturbance C0238357 Hyperkalemic periodic paralysis HPO C4085317 Diarrhea frequency C0950123 Inborn genetic disease HSDN C0557874 Global developmental delay C1864663 Hypomyelination and congenital cataract OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards|HPO C4084774 Have weight loss C0153415 Malignant neoplasm of lower third of esophagus MalaCards C4084784 Diarrhea C1367460 Lats1 gene HSDN C0917816 Deficiency mental C2931296 Yorifuji okuno syndrome OrphaNet|HPO C0231528 Muscle pain generalized C1522133 High cholesterol level HSDN C2919142 Short stature adverse event C0795953 Masa syndrome (disorder) OrphaNet|HPO|MalaCards C1069915 Vertigo C0035460 Rhinitis, vasomotor HSDN C4084802 Usual severity diarrhea C0034040 Puerperal disorders HSDN C4084727 Cough frequency C3203727 Pneumorrhachi HSDN C0026821 Cramp C0042870 Vitamin d deficiency HSDN C0009398 Color vision defects C0497327 Dementia HSDN C3898969 Have been vomiting C2240378 Cleft palate on exam HSDN C0004941 Behavioral symptoms C1842870 Chromosome 1p36 deletion syndrome OrphaNet C2242996 Tingling C0043145 Whiplash HSDN C1549543 Administration method - pain C0026691 Mucocutaneous lymph node syndrome HSDN C0700078 Deep tendon reflex decrease C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0023440 Acute erythroblastic leukemia HSDN C2919142 Short stature adverse event C2750080 Diamond-blackfan anemia 10 MalaCards|HPO C0030552 Paralysis partial C0085388 Intracranial tuberculoma HSDN C1963093 Dizziness adverse event C0013806 Electroplexy shock therapy HSDN C3539892 Pelvic pain in front C0020517 Hypersensitivity HSDN C0015300 Ocular proptosis C1970458 Osteogenesis imperfecta, type viii HPO C4042891 Sleep wake disorders C0233610 Negativism in catatonia HSDN C0032617 High urine output C0022660 Kidney failure, acute UMLS C2237041 Shox gene with short stature C3151126 Meier-gorlin syndrome 5 MalaCards C4084775 Usual severity weight loss C0149514 Bronchitis acute HSDN C0007166 Cardiac output decreased C0238417 Scorpion sting HSDN C0013144 Drowsy C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards C4085661 Usual severity nausea C0524620 Metabolic syndrome x HSDN C0037763 Spasm C0018939 Hematological disease HSDN C0020505 Excessive eating C0338451 Frontotemporal dementia HPO C2984058 Have pain C0038187 Starvation HSDN C0002962 Angina C0238154 Epidural hematoma HSDN C0018926 Emesis bloody C0027651 Tumor HSDN C0242936 Center pain C0002884 Hypochromic anemia HSDN C0155002 Vision loss acute C0001314 Acute disease UMLS C0234146 Absent reflex C0085404 Poems syndrome MalaCards C0027497 Queasy C1963067 Atrial fibrillation adverse event HSDN C2024893 Cardiovascular surgery result: fatigue C0342257 Complications of diabetes mellitus HSDN C2984057 Have nausea C0001403 Addison disease HSDN C4084774 Have weight loss C0019087 Hemorrhagic disorders HSDN C0036572 Convulsion C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0020672 Body temperature decreased C0080179 Vertebra fracture HSDN C3641756 Have diarrhea C0037199 Sinusitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0342443 Adrenal cushing's syndrome HSDN C4084766 Vomiting C1533628 Pseudo-zellweger syndrome MalaCards C1557397 Adverse event associated with pain C0752140 Intracranial embolism HSDN C0424755 Fever symptoms C2963140 Arteriovenous fistula in use with two needles HSDN C1384666 Decreased hearing C1258104 Diffuse scleroderma HSDN C0162834 Hyperpigmentation C1868019 Adenomatous polyposis coli, attenuated HPO C0007758 Cerebellar ataxia C1720864 Sulfatidosis, juvenile, austin type MalaCards|HPO C1963281 Vomiting adverse event C0017152 Gastritis HSDN C0020903 Illusion C0034931 Reflex sympathetic dystrophy HSDN C1962972 Proteinuria adverse event C0006663 Calcinosis HSDN C0349588 Stature short C4015242 Retinal dystrophy, juvenile cataracts, and short stature syndrome MalaCards C1963184 Nystagmus adverse event C0162809 Kallmann syndrome OrphaNet|HPO|MalaCards C0162298 Stiffness joints C0014084 Enchondromatosis OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0030920 Peptic ulcer HSDN C0009421 Comatose C0037198 Sinus thrombosis, intracranial HSDN C0035229 Respiratory function impaired C0796274 Brown-vialetto-van laere syndrome OrphaNet|HPO|MalaCards C0424755 Fever symptoms C0034882 Rectal diseases HSDN C0857305 Thrombocytopenia purpura C0027051 Myocardial infarction HSDN C0034150 Skin purpura C0051981 Anti-leprosy vaccine HSDN C0231218 Malaise generalized C0279067 Angiocentric immunoproliferative lesion grade iii UMLS C4084726 Distress cough C0009447 Common variable immunodeficiency HSDN C0034150 Skin purpura C0003873 Rheumatoid arthritis HSDN C1963086 Confusion adverse event C0004626 Pneumonia, bacterial HSDN C1557397 Adverse event associated with pain C1527311 Brain edema HSDN C0023015 Language handicap C0018674 Head trauma HSDN C0557874 Global developmental delay C3150790 Chromosome 6q11-q14 deletion syndrome MalaCards C3887873 Hearing loss C1546533 Specimen source codes - abscess HSDN C4085211 Pain distress question C0022570 Keratitis dentritic HSDN C2911647 Weight gain adverse event C0021831 Intestinal diseases HSDN C0424755 Fever symptoms C1963198 Pancreatitis adverse event HSDN C4085211 Pain distress question C0042384 Vasculitis HSDN C3887873 Hearing loss C0007137 Squamous cell carcinoma HSDN C0020673 Hypothermia (central) (local) C1384607 Food deprivation HSDN C0009676 Confusion state C0012979 Canine disease HSDN C3665386 Abnormal vision C1864205 Macular degeneration, age-related, 1 MalaCards C0022346 Yellow skin C1458156 Recurrent malignant neoplasm HSDN C4084784 Diarrhea C0028077 Night blindness HSDN C2242996 Tingling C0752235 Lyme neuroborreliosis MalaCards C4085222 Nausea C1963119 Stomach ulcer adverse event HSDN C0009806 Constipate C0376547 Aromatherapy HSDN C4084724 Usual severity constipation C0033247 Proctocolitis HSDN C0003962 Ascites C0343206 Hypocomplementemic urticarial vasculitis MalaCards C3641755 Have constipation C1866927 Smcr HPO C0024031 Back pain lower back C0013808 Electroconvulsive therapy HSDN C0036572 Convulsion C3897747 Recurrent childhood oligodendroglioma UMLS C0575081 Abnormal gait C1970840 Leukoencephalopathy with metaphyseal chondrodysplasia MalaCards C0040822 D tremors C0242350 Erectile dysfunction HSDN C0029163 Hemorrhage mouth C1442903 Exostoses HSDN C0008031 Pain chest C0011882 Diabetic neuropathies UMLS C3665347 Vision impaired C1858677 Leber congenital amaurosis 3 (disorder) MalaCards|HPO C0020458 Hyperhydrosis C0017075 Ganglioneuroma MalaCards C4084726 Distress cough C0031149 Peritoneal neoplasms HSDN C0039070 Collapse fleeting C0031347 Pharyngeal neoplasms HSDN C0240735 Personality change C1847967 Ovarioleukodystrophy MalaCards|HPO C0018772 Deafness C0751667 Canavan disease, juvenile MalaCards C0005745 Blepharoptosis C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C4084767 Bothered by vomiting C0268293 Corticosterone methyl oxidase type i deficiency HPO C0151786 Weakness muscle C3714644 Thymus neoplasms HSDN C2911647 Weight gain adverse event C3244301 Coverage level - family HSDN C4084769 Vomiting frequency C0023817 Hyperlipoproteinemia type i HPO C0424755 Fever symptoms C1858361 Pyogenic arthritis, pyoderma gangrenosum and acne OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0238163 Hereditary hyperphosphatasia MalaCards C2911645 Weight loss adverse event C0221056 Adult type dermatomyositis OrphaNet|HSDN|MalaCards C0004134 Dyssynergia C1862596 Familial hypobetalipoproteinemia MalaCards|UMLS C0015300 Ocular proptosis C2677099 Crouzon syndrome with acanthosis nigricans (disorder) OrphaNet|HPO|MalaCards C1963093 Dizziness adverse event C0014852 Esophageal diseases HSDN C2911647 Weight gain adverse event C0001824 Agranulocytosis HSDN C0152116 Torticollis spasmodic C1843264 Dystonia 13, torsion OrphaNet|MalaCards C0085602 Polydypsia C0011880 Diabetic ketoacidosis UMLS C4085222 Nausea C0025345 Menstruation disturbances HSDN C0240735 Personality change C0282513 Primary progressive aphasia (disorder) HPO C0042963 Symptoms vomiting C0021400 Influenza HSDN C1963091 Diarrhea adverse event C0016952 Galactosemias MalaCards C1384666 Decreased hearing C1275081 Cardio-facio-cutaneous syndrome HPO C3815497 Cough C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0460137 Push down or depress C1439329 Cbs gene HPO C3641756 Have diarrhea C0013990 Pathological accumulation of air in tissues HSDN C1971624 Appetite absent C0025427 Mercury poisoning OrphaNet|MalaCards C4085211 Pain distress question C1510412 Pseudoaneurysm HSDN C0018772 Deafness C0266004 Knuckle pads, leuconychia and sensorineural deafness HPO C3829611 Nausea frequency C0004623 Bacterial infections HSDN C0013604 Edematous C0035243 Respiratory tract infections HSDN C4084768 Usual severity vomiting C0021845 Intestinal perforation HSDN C1963184 Nystagmus adverse event C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0009398 Color vision defects C1547046 Kind of quantity - taste HSDN C3815497 Cough C1720777 Functional laterality HSDN C2029884 Hearing loss by exam C0051981 Anti-leprosy vaccine HSDN C0595939 Stillborn C0392475 Roberts-sc phocomelia syndrome HPO C0037199 Sinus infection C0268125 Purine-nucleoside phosphorylase deficiency HPO C0034150 Skin purpura C0022602 Actinic keratosis HSDN C3463815 Feel fatigue C0038012 Spondylitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003128 Anovulation HSDN C0234784 Reflex gag absent C0015708 Fazio londe syndrome MalaCards C4085661 Usual severity nausea C1546533 Specimen source codes - abscess HSDN C0004134 Dyssynergia C0524910 Hepatitis c, chronic HSDN C3829611 Nausea frequency C1704436 Peripheral arterial diseases HSDN C4085210 Usual severity pain C0040961 Tricuspid valve insufficiency HSDN C4042891 Sleep wake disorders C0013808 Electroconvulsive therapy HSDN C0000737 Abdomen pain C0267797 Acute hepatitis UMLS C0349588 Stature short C1848068 Mental retardation, x linked, with isolated growth hormone deficiency HPO C0007758 Cerebellar ataxia C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C0518090 Frequency of pain question C0022570 Keratitis dentritic HSDN C0003862 Pain joint C2930674 Babesioses, human MalaCards C0242936 Center pain C0023267 Fibroid tumor HSDN C0030486 Extremity paralysis, lower C0700095 Central neuroblastoma HSDN C4085317 Diarrhea frequency C0006264 Bronchial neoplasms HSDN C0557874 Global developmental delay C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C0085631 Abnormal excitement C0243026 Sepsis HSDN C0042963 Symptoms vomiting C0015457 Expression facial HSDN C0152116 Torticollis spasmodic C0521518 Muscle spasms of head and neck UMLS C2024878 Cardiovascular surgery result: dyspnea C1881674 Medical device emits smoke HSDN C0039231 Heartbeats increased C3539003 Neuropathy, hereditary sensory and autonomic, type vi MalaCards C2203646 Jaundice C1843116 Bile acid synthesis defect, congenital, 1 OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C1142166 Brugada syndrome (disorder) HSDN C0034150 Skin purpura C0029456 Osteoporosis HSDN C0018772 Deafness C0011265 Presenile dementia HSDN C0557874 Global developmental delay C2678194 Mental retardation, x-linked, syndromic, christianson type HPO C2024893 Cardiovascular surgery result: fatigue C0032914 Pre-eclampsia HSDN C0008031 Pain chest C0155626 Acute myocardial infarction UMLS C2911645 Weight loss adverse event C0023440 Acute erythroblastic leukemia HSDN C0006370 Bulimia C0086045 Concentration HSDN C2024878 Cardiovascular surgery result: dyspnea C0019557 Hip fx HSDN C0019209 Large liver C0345904 Malignant neoplasm of liver MalaCards C0234512 Prosopagnosia C0935573 Mind theory HSDN C0034124 Pupillary disorder C0022972 Lambert-eaton myasthenic syndrome HSDN C0035229 Respiratory function impaired C0158683 Polycystic liver disease MalaCards|HPO C1963087 Constipation adverse event C0007133 Carcinoma, papillary HSDN C4085210 Usual severity pain C0011175 Dehydration HSDN C0030193 Sense of pain C0013377 Dysgerminoma HSDN C0233565 Bradykinesia C3280133 Parkinson disease 17 MalaCards|UMLS C4084724 Usual severity constipation C0343376 B; paratyphoid fever DiseaseOntology|MalaCards C1557397 Adverse event associated with pain C0221204 Lytic lesion HSDN C4084802 Usual severity diarrhea C0014342 Bluecomb of turkeys HSDN C0010520 Skin cyanosis C2945560 Hemolytic HSDN C0349588 Stature short C3150644 Brachydactyly, type e2 MalaCards|HPO C2919142 Short stature adverse event C3278481 Microcephaly and chorioretinopathy, autosomal recessive, 1 MalaCards C0019825 Voice hoarseness C1096902 Infantile sialic acid storage disease MalaCards C1860844 Sparse, thin hair C0796038 Mcdonough syndrome MalaCards C0157536 Childbed fever C0810050 Other complications of birth; puerperium affecting management of mother UMLS C4084788 Have dizziness C0023055 Laryngeal neoplasm HSDN C3274924 Have been coughing C0027819 Neuroblastoma HSDN C4084724 Usual severity constipation C1963198 Pancreatitis adverse event HSDN C0010520 Skin cyanosis C0027149 Myxoma HSDN C0015676 Mental fatigue C2713543 Biofeedback eeg HSDN C4084723 Constipation C0027149 Myxoma HSDN C3887638 Failure to thrive in infant C0265268 Adams oliver syndrome OrphaNet|HPO|MalaCards C0042940 Disorder of voice C0040136 Thyroid neoplasm HSDN C0727671 Red cross toothache drops C0022362 Jaw diseases HSDN C0795692 Lactate blood increased C0524909 Hepatitis b, chronic HSDN C0023012 Delay language C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0019079 Bloody sputum C0520538 Tracheobronchopathia osteoplastica MalaCards C1963064 Anxiety adverse event C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0003857 Congenital arteriovenous malformation HSDN C0413252 Hypothermia due to exposure C0020255 Hydrocephalus HSDN C0018681 Headache, cephalalgia C2749559 Methemoglobinemia, type i HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0023269 Leiomyosarcoma HSDN C0039070 Collapse fleeting C0036421 Systemic scleroderma HSDN C3887638 Failure to thrive in infant C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0042798 Vision dim C0009363 Congenital ocular coloboma (disorder) HSDN|HPO C0233514 Behavior abnormal C3275495 Kabuk2 MalaCards C0013604 Edematous C0238154 Epidural hematoma HSDN C0036572 Convulsion C0477370 Oth gen epilep + epilep syn UMLS C0009676 Confusion state C0042138 Uterine neoplasms HSDN C0917816 Deficiency mental C1832735 Bindewald ulmer muller syndrome MalaCards C0023380 Lethargy C0270855 Early myoclonic encephalopathy OrphaNet|HPO|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0020676 Hypothyroidism HSDN C2029884 Hearing loss by exam C0424688 Small head HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0002895 Anemia, sickle cell OrphaNet|HPO|MalaCards C4084784 Diarrhea C0019569 Hirschsprung disease MalaCards|HSDN|HPO C0241210 Speaking delay C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C0027497 Queasy C0554114 Epstein-barr virus hepatitis MalaCards C0024031 Back pain lower back C0029422 Osteochondrodysplasias HSDN C0016199 Pain flank C0025568 Metaplasia HSDN C1963065 Apnea adverse event C0812393 Cancer patients and suicide and depression HSDN C1549543 Administration method - pain C1136321 Hiv-associated lipodystrophy syndrome HSDN C0020438 Hypercalciuria C1840403 Parathyroid adenoma, familial OrphaNet C1963281 Vomiting adverse event C0024636 Malocclusion HSDN C0018780 Frequencies hearing high loss C0040427 Tooth abnormalities HSDN C2242996 Tingling C0021670 Insulinoma MalaCards|HPO C4084766 Vomiting C0036118 Salmonella infections, animal HSDN C3539889 Pelvic pain increasing in severity C0042341 Varicocele HSDN C0917816 Deficiency mental C1848201 Subcortical band heterotopia HPO C0700078 Deep tendon reflex decrease C1836485 Charcot-marie-tooth disease, axonal, type 2a2 (disorder) HPO C1963071 Back pain adverse event C0011071 Sudden death HSDN C0003862 Pain joint C0007789 Cerebral palsy HSDN C0029163 Hemorrhage mouth C0003969 Ascorbic acid deficiency HSDN C2315100 Pediatric failure to thrive C2749175 Mineralocorticoid deficiency, isolated HPO C0037763 Spasm C0152156 Dystocia HSDN C0518090 Frequency of pain question C0263843 Band iliotibial syndromes HSDN C0004604 Pain back C0021368 Inflammation HSDN C0013395 Indigestion C1333791 Gastric tubular adenocarcinoma UMLS C1961131 Cough adverse event C3178892 Disease, pelvic floor HSDN C4042891 Sleep wake disorders C0022758 Kap HSDN C0010520 Skin cyanosis C0014544 Epilepsy HSDN C0019079 Bloody sputum C0019080 Hemorrhage UMLS C2032396 Pelvic pain on the right C0010709 Cyst HSDN C0231528 Muscle pain generalized C2936781 Generalized myotonia of thomsen HPO C0020305 Fetal edema C3812171 Bradycardia by ecg finding HSDN C1557397 Adverse event associated with pain C1963059 Adrenal insufficiency adverse event HSDN C0575081 Abnormal gait C1859069 Brittle bone disorder OrphaNet C0032617 High urine output C3245525 Familial renal glucosuria MalaCards C2919142 Short stature adverse event C1859252 Cerebrofaciothoracic dysplasia OrphaNet|HPO|MalaCards C3815497 Cough C1704272 Benign prostatic hyperplasia HSDN C4084766 Vomiting C0853697 Neutrophil count decreased HSDN C1962972 Proteinuria adverse event C0038941 Incisional infection HSDN C0026838 Spasticity muscle C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards|UMLS C4084727 Cough frequency C0001175 Acquired immunodeficiency syndrome HSDN C2984058 Have pain C0037052 Sick sinus syndrome HSDN C1260880 Nasal drip C0740487 Sinus, maxillary, cancer, carcinoma UMLS C0424755 Fever symptoms C0936250 Eczema herpeticum DiseaseOntology|MalaCards C0027497 Queasy C0023283 Leishmaniasis, cutaneous HSDN C0006370 Bulimia C0037051 Behavior illness HSDN C0392678 Impaired swallowing C0011168 Deglutition disorders UMLS C0037036 Increased salivation C0162635 Angelman syndrome MalaCards|HPO C0007758 Cerebellar ataxia C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0018784 Deafness sensorineural C1857572 Corneal dystrophy and perceptive deafness OrphaNet|HPO C2315100 Pediatric failure to thrive C3277723 Joubert syndrome 12 MalaCards C0413252 Hypothermia due to exposure C0005591 Avian disease HSDN C1384666 Decreased hearing C2931254 Alport syndrome, recessive type MalaCards C4085222 Nausea C0024788 Green monkey virus disease DiseaseOntology|MalaCards C0007758 Cerebellar ataxia C2751318 Nijmegen breakage syndrome-like disorder MalaCards|HPO C0000737 Abdomen pain C0019101 Hemorrhagic fever with renal syndrome OrphaNet|MalaCards C0036572 Convulsion C0393697 Epilepsy; grand mal, on awakening UMLS C0428977 Pulse rate decrease C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards|HPO C0010520 Skin cyanosis C0023467 Leukemia, myelocytic, acute HSDN C0086565 Liver function abnormal C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism MalaCards C0497406 Over weight C0007131 Non-small cell lung carcinoma HSDN C0015230 Exanthem C3887645 Job syndrome OrphaNet|HPO C0036572 Convulsion C3150419 Nephronophthisis-like nephropathy 1 MalaCards|HPO C1971624 Appetite absent C0011881 Diabetic nephropathy HSDN C2032396 Pelvic pain on the right C0243001 Abdominal abscess HSDN C1549543 Administration method - pain C0006849 Oral candidiasis HSDN C0018926 Emesis bloody C0158570 Vascular anomaly HSDN C0030554 Abnormal sensation C1112155 Hereditary non-polyposis colorectal cancer syndrome HPO C0030193 Sense of pain C0206752 Alphavirus infections HSDN C0000737 Abdomen pain C0007350 Cat disease HSDN C3898969 Have been vomiting C0021359 Infertility HSDN C0497406 Over weight C0036202 Sarcoidosis HSDN C0853945 Oral mucosa blister C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C0427055 Face weakness C3554478 Osteopetrosis, autosomal recessive 8 MalaCards C0011991 Loose stools C0023092 Lassa fever OrphaNet|MalaCards C0518090 Frequency of pain question C0013505 Cyst, pulmonary hydatid HSDN C0004604 Pain back C0024314 Lymphoproliferative disorders HSDN C0024031 Back pain lower back C0032269 Pneumococcal infections HSDN C0013395 Indigestion C0012979 Canine disease HSDN C0522224 Palsied C0023269 Leiomyosarcoma HSDN C2024893 Cardiovascular surgery result: fatigue C0002792 Anaphylaxis HSDN C4085210 Usual severity pain C0016079 Figural aftereffects HSDN C2919142 Short stature adverse event C2677903 Mental retardation and microcephaly with pontine and cerebellar hypoplasia MalaCards|HPO C2919142 Short stature adverse event C3146244 Alcohol related birth defect OrphaNet|MalaCards C0013604 Edematous C0013292 Obstruction duodenal HSDN C1963087 Constipation adverse event C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C4084768 Usual severity vomiting C0042812 Acuity visual HSDN C0008031 Pain chest C0007570 Celiac disease HSDN C0027498 Nausea vomiting C0795887 Chromosome xp21 deletion syndrome MalaCards C0033377 Caudal displacement C0814154 Alcohol-related neurodevelopmental disorder OrphaNet|MalaCards C0004134 Dyssynergia C1090821 Sepsis (invertebrate) HSDN C1384666 Decreased hearing C0041948 Uremia HSDN C0030193 Sense of pain C0006266 Bronchial spasm HSDN C2984057 Have nausea C0028796 Dermatitis, occupational HSDN C4085211 Pain distress question C0751895 Vasospasm, intracranial HSDN C1557397 Adverse event associated with pain C0017178 Gastrointestinal diseases HSDN C0860603 Anxiety symptom C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C0018772 Deafness C0007787 Transient ischemic attack HSDN C2984058 Have pain C0013182 Drug allergy HSDN C3539893 Pelvic pain occurs with intercourse C2706915 Language:-:point in time:^patient:- HSDN C4085210 Usual severity pain C0376378 Barre lieou syndrome HSDN C3641755 Have constipation C2911243 Encounter due to family history of colonic polyps HSDN C4084775 Usual severity weight loss C0003838 Arterial occlusive diseases HSDN C2911645 Weight loss adverse event C0023895 Liver diseases HSDN C0036572 Convulsion C2677589 Spinocerebellar ataxia, autosomal recessive 9 MalaCards|HPO C0030552 Paralysis partial C1527406 Rhizomelic pseudopolyarthritis MalaCards C4085210 Usual severity pain C1705812 Nci thesaurus role HSDN C4084769 Vomiting frequency C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C4084769 Vomiting frequency C0023441 Leukemia, experimental HSDN C4042891 Sleep wake disorders C0220847 C hepatitis virus HSDN C0013604 Edematous C0032578 Polyploidy HSDN C0011206 Delirium acute C0038941 Incisional infection HSDN C0000737 Abdomen pain C0079027 Blood loss, surgical HSDN C4084784 Diarrhea C3469186 Hemochromatosis, type 1 HSDN C2029884 Hearing loss by exam C0023364 Leptospirosis HSDN C4084767 Bothered by vomiting C0042470 Guanarito haemorrhagic fever MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0002886 Anemia, macrocytic HSDN C1579931 Depressed - symptom C0085209 Bovine spongiform encephalitis MalaCards C0005745 Blepharoptosis C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0242936 Center pain C0011351 Dental enamel hypoplasia HSDN C1963071 Back pain adverse event C0038454 Cerebrovascular accident HSDN C2024893 Cardiovascular surgery result: fatigue C1710146 Familial spinal arachnoiditis MalaCards C2237041 Shox gene with short stature C0796046 Mental retardation-epilepsy-short stature-skeletal dysplasia syndrome OrphaNet|MalaCards C1069915 Vertigo C0262655 Recurrent urinary tract infection HSDN C0037316 Not enough sleeping C0007384 Cataplexy HSDN C0010200 Cough symptom C2931916 Midline granulomatosis MalaCards C1963063 Anorexia adverse event C1458155 Mammary neoplasms HSDN C0857305 Thrombocytopenia purpura C0014544 Epilepsy HSDN C2363731 Oropharyngeal pain C0155825 Sore throat chronic UMLS C4084793 Have hair loss C1148551 X-linked dyskeratosis congenita MalaCards C4085661 Usual severity nausea C0023434 Chronic lymphocytic leukemia HSDN C0086437 Joint hypermobility C1848862 Miller-mckusick-malvaux-syndrome (3m syndrome) HPO C1961131 Cough adverse event C3179093 Injuries, laryngeal nerve HSDN C3898969 Have been vomiting C0031212 Personality disorders HSDN C4084769 Vomiting frequency C0022758 Kap HSDN C0413252 Hypothermia due to exposure C0010068 Coronary heart disease HSDN C0018991 Paralysis one side of body C0751955 Brain infarction HSDN C0020580 Decreased sensation C0025202 Melanoma HSDN C4084726 Distress cough C0343206 Hypocomplementemic urticarial vasculitis MalaCards C4084726 Distress cough C0038187 Starvation HSDN C0009806 Constipate C2713392 Phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency HPO C2024878 Cardiovascular surgery result: dyspnea C0007273 Carotid artery diseases HSDN C4085210 Usual severity pain C0276926 Schistosoma hematobium infection HSDN C1384666 Decreased hearing C3808975 Hypogonadotropic hypogonadism 18 with or without anosmia MalaCards C0243026 Generalized infection C0398738 Leukocyte adhesion deficiency type 1 MalaCards C3665347 Vision impaired C3809877 Schaaf-yang syndrome MalaCards C0009792 Consciousness disorder C0032587 Polyradiculoneuropathy HSDN C0600142 Flash hot C0002395 Alzheimer's disease HSDN C0004604 Pain back C0018571 Hand injury HSDN C0557874 Global developmental delay C3711390 9q22 deletion syndrome OrphaNet|HPO|MalaCards C1961131 Cough adverse event C1864997 Majeed syndrome MalaCards|HPO C0151786 Weakness muscle C0206138 Crest syndrome HSDN C4084784 Diarrhea C0002874 Aplastic anemia HSDN C0018772 Deafness C0024314 Lymphoproliferative disorders HSDN C0015672 Decreased energy C0221043 Liddle syndrome OrphaNet|HPO|MalaCards C0037316 Not enough sleeping C0030508 Parasomnia HSDN C0011991 Loose stools C0220754 Biotinidase deficiency MalaCards|HPO|UMLS C0013604 Edematous C0700095 Central neuroblastoma HSDN C0231835 Respiration rate increased C0023518 Leukocytosis HSDN C3146279 Coma C0007787 Transient ischemic attack HSDN C1963093 Dizziness adverse event C2911643 Encounter due to family history of osteoporosis HSDN C0015469 Facial paralysis C1260409 Myasthenia gravis without acute exacerbation MalaCards C0575081 Abnormal gait C2680446 Spastic paraplegia 43, autosomal recessive MalaCards C0011991 Loose stools C0206624 Hepatoblastoma MalaCards C0575081 Abnormal gait C0268250 Gaucher disease, type 2 (disorder) MalaCards C0036572 Convulsion C1859499 3-methylcrotonyl coa carboxylase 2 deficiency MalaCards|UMLS C0010200 Cough symptom C0025063 Mediastinal neoplasms HSDN C0018991 Paralysis one side of body C0012644 Animal disease models HSDN C0242936 Center pain C0151526 Premature birth HSDN C4085211 Pain distress question C0013806 Electroplexy shock therapy HSDN C1860844 Sparse, thin hair C3150874 Cranioectodermal dysplasia 2 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C1961131 Cough adverse event C0001418 Adenocarcinoma HSDN C0015676 Mental fatigue C0031207 Personal space HSDN C0027796 Neuralgias C0009759 Conjunctival diseases HSDN C1963252 Tremor adverse event C0795623 Hepatitis a vaccine, inactivated HSDN C0282005 Scrotum swelling C0152814 Epididymal tuberculosis MalaCards C0150055 Pain chronic C0041296 Tuberculosis HSDN C4084727 Cough frequency C0037355 Smallpox vaccines HSDN C0027497 Queasy C0021847 Intestinal pseudo-obstruction HSDN C0518090 Frequency of pain question C0014858 Esophageal motility disorders HSDN C4084769 Vomiting frequency C4085635 Appetite quality question HSDN C0242936 Center pain C0032578 Polyploidy HSDN C1963247 Ventricular tachycardia adverse event C1832680 Cardiomyopathy, dilated, 1e MalaCards C0019209 Large liver C0472767 Beta thalassemia intermedia OrphaNet|HPO C0015676 Mental fatigue C0038441 Stress disorders, traumatic HSDN C4085210 Usual severity pain C0004943 Behcet syndrome HSDN C0036572 Convulsion C0001206 Acromegaly HSDN C2029884 Hearing loss by exam C0024117 Chronic obstructive airway disease HSDN C1279888 Proteinuria of undiagnosed cause C3711749 Nonsyndromic holoprosencephaly MalaCards C0006370 Bulimia C4050613 Anxiety scale (basc-2) HSDN C3274924 Have been coughing C0009375 Colonic neoplasms HSDN C1963170 Hypothermia adverse event C0007117 Basal cell carcinoma HSDN C0030486 Extremity paralysis, lower C0004610 Bacteremia HSDN C0013132 Drooling C0035410 Rhabdomyolysis MalaCards C0030552 Paralysis partial C0014547 Epilepsies, partial HSDN C0024031 Back pain lower back C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0495682 Cramp and spasm C0810058 Other connective tissue disease UMLS C0011991 Loose stools C1962983 Cataract adverse event HSDN C0085632 Listlessness C1842704 Gaucher disease, perinatal lethal MalaCards|HPO|UMLS C4084788 Have dizziness C0015464 Facial nerve diseases HSDN C0007758 Cerebellar ataxia C0268138 Xeroderma pigmentosum, complementation group d HPO C0020305 Fetal edema C0268250 Gaucher disease, type 2 (disorder) MalaCards C0009806 Constipate C0037650 Somatoform disorder HSDN C4084767 Bothered by vomiting C0038159 Food poisoning, staphylococcal DiseaseOntology|MalaCards C4085211 Pain distress question C0033968 Psychotherapeutic technique HSDN C0033377 Caudal displacement C1859432 Blepharophimosis with ptosis, syndactyly, and short stature OrphaNet|MalaCards C2984057 Have nausea C3814778 Hemolytic index HSDN C4085317 Diarrhea frequency C1832322 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive HPO C0004134 Dyssynergia C0221061 Behr syndrome OrphaNet|HPO|MalaCards C0151889 Reflexes tendon increased C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0015230 Exanthem C0406234 Inverse pattern atopic dermatitis UMLS C0439029 Deafness symptom C0870387 Blind deaf UMLS C0851578 Disorder sleep C0029132 Disorder of the optic nerve HSDN C0018784 Deafness sensorineural C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C2984058 Have pain C0037019 Shy-drager syndrome HSDN C0085631 Abnormal excitement C0041327 Tuberculosis, pulmonary HSDN C0497406 Over weight C0233315 Premature birth of newborn HSDN C0162285 Edema eyelid C0342200 Endemic cretinism MalaCards C1963184 Nystagmus adverse event C3889636 Spinocerebellar ataxia 37 MalaCards C0917816 Deficiency mental C2931638 Chromosome 8, monosomy 8p23 1 MalaCards C0013604 Edematous C0042826 Field visual HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030767 Grouping peer HSDN C0917816 Deficiency mental C3711390 9q22 deletion syndrome OrphaNet|HPO|MalaCards C0042024 Urine incontinence C0032708 Disorders of porphyrin metabolism HSDN C0033774 Skin pruritus C0042830 Perception visual HSDN C0027066 Myoclonic jerking C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0011991 Loose stools C0004114 Astrocytoma HSDN C4084766 Vomiting C0021833 Intestinal fistula HSDN C4085548 Usual severity dizziness C4048184 Trochlear nerve diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010276 Craniopharyngioma HSDN C0018777 Deafness, conductive C0012979 Canine disease HSDN C3887638 Failure to thrive in infant C0268193 Nadh cytochrome b5 reductase deficiency MalaCards C0018784 Deafness sensorineural C3809216 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 MalaCards C4084776 Weight loss C0020295 Hydronephrosis HSDN C4084775 Usual severity weight loss C0022602 Actinic keratosis HSDN C0518090 Frequency of pain question C0017572 Gingival recession HSDN C0349588 Stature short C0220722 Cerebrooculofacioskeletal syndrome 1 OrphaNet|HPO C0013132 Drooling C3502054 Dentoleukoencephalopathy MalaCards C4085317 Diarrhea frequency C0030500 Animal parasitic disease HSDN C0042963 Symptoms vomiting C1963198 Pancreatitis adverse event HSDN C0036572 Convulsion C3275954 Lacht MalaCards C0851578 Disorder sleep C0520946 Emotional hypersensitivity HSDN C0860603 Anxiety symptom C0016667 Fragile x syndrome MalaCards|HPO C4085210 Usual severity pain C0001206 Acromegaly HSDN C1961131 Cough adverse event C0014854 Esophageal diverticulum HSDN C1963091 Diarrhea adverse event C0033953 Psychosexual disorders HSDN C1260880 Nasal drip C1711278 Nasopharyngeal papillary adenocarcinoma UMLS C4084766 Vomiting C0042035 Urination disorders HSDN C4084725 Usual severity cough C0854421 Hanta viral infections MalaCards C1963252 Tremor adverse event C0752219 Axonal diffuse injury HSDN C0013404 Respiratory difficulty C0854994 Metastatic epidermoid cell carcinoma of lung UMLS C0277967 Adipsia C0013473 Eating disorders UMLS C0034150 Skin purpura C1962979 Burn adverse event HSDN C4085317 Diarrhea frequency C0032787 Postoperative complications HSDN C3887638 Failure to thrive in infant C1855861 Glycogen storage disease 0, liver MalaCards C1963091 Diarrhea adverse event C0040592 Trachoma HSDN C0239182 Diarrhea watery C4015130 Inflammatory skin and bowel disease, neonatal, 2 MalaCards|UMLS C0018991 Paralysis one side of body C0014714 Ergotism HSDN C2024878 Cardiovascular surgery result: dyspnea C1547046 Kind of quantity - taste HSDN C4084724 Usual severity constipation C0036323 Schistosomiasis HSDN C0270948 Neurogenic muscular atrophy C1306214 Acth-secreting pituitary adenoma HPO C0036659 Sensation disorder C1963064 Anxiety adverse event HSDN C0518090 Frequency of pain question C0017574 Gingivitis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007820 Cerebrovascular disorders HSDN C0033774 Skin pruritus C0001145 Acne keloid HSDN C1963281 Vomiting adverse event C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO C0027066 Myoclonic jerking C0019360 Herpes zoster disease HSDN C0398650 Idiopathic thrombocytopenia purpura C0004161 Athletic injuries HSDN C4085210 Usual severity pain C0032227 Pleural effusion disorder HSDN C0575081 Abnormal gait C0175702 Williams syndrome OrphaNet|MalaCards C4084769 Vomiting frequency C0520799 Acute radiation syndrome HSDN C0037383 Sneeze C0460136 Barotrauma HSDN C0557874 Global developmental delay C0265287 Acromicric dysplasia HPO C0151686 Growth retardation C1846265 Microphthalmia, syndromic 2 MalaCards C2242996 Tingling C0027804 Fatigue neurosis HSDN C0728710 Pupil constriction observed C0017601 Glaucomas HSDN C4084766 Vomiting C1135868 Gestational trophoblastic neoplasms HSDN C4084723 Constipation C1548484 Rheumatic fever vaccine HSDN C4085862 Bothered by nausea C0453996 Tobacco smoking HSDN C0151786 Weakness muscle C0149925 Small cell carcinoma of lung HSDN C0027066 Myoclonic jerking C4225258 Epilepsy, progressive myoclonic, 10 UMLS C2203646 Jaundice C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0234144 Dysgraphia C1843891 Spinocerebellar ataxia 21 HPO C0029163 Hemorrhage mouth C0302148 Blood clot HSDN C0009676 Confusion state C0752143 Intracranial thrombosis HSDN C4049644 Depression C3554605 Mc3dn2 MalaCards C0002962 Angina C0518449 Control of hip fracture risk HSDN C1279888 Proteinuria of undiagnosed cause C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0413252 Hypothermia due to exposure C2240374 Eosinophil count raised HSDN C0036572 Convulsion C3542499 Aminoacylase 2 deficiency MalaCards C0002962 Angina C0152417 Congenital stenosis aortic valve MalaCards C0020649 Blood pressure decreased C0024620 Primary malignant neoplasm of liver MalaCards C4084766 Vomiting C0032461 Polycythemia HSDN C4084773 Bothered by weight gain C0003811 Cardiac arrhythmia HSDN C3494358 Characteristic, prodromal C0524851 Neurodegenerative disorders HSDN C1549543 Administration method - pain C0012546 Diphtheria HSDN C1962972 Proteinuria adverse event C0008728 Churg-strauss syndrome MalaCards C0151889 Reflexes tendon increased C1846492 Spinocerebellar ataxia, autosomal recessive 4 MalaCards C0020796 Profoundly mentally retarded C2677109 Leukodystrophy, hypomyelinating, 4 MalaCards|HPO C0003862 Pain joint C1304205 Neutrophilic urticaria MalaCards C0000737 Abdomen pain C1266119 Solitary fibrous tumor HSDN C4084766 Vomiting C0542241 Toxemia bacterial HSDN C0151889 Reflexes tendon increased C2749936 Spastic paraplegia 18, autosomal recessive (disorder) MalaCards|HPO C4084768 Usual severity vomiting C0022821 Kyphosis deformity of spine HSDN C0004134 Dyssynergia C0007134 Renal cell carcinoma HSDN C0149651 Clubbing C1274675 Acquired hippocratic nails UMLS C0036572 Convulsion C0234541 Cry, epileptic UMLS C0010200 Cough symptom C0010414 Infection by cryptococcus neoformans HSDN C1963137 Hydrocephalus adverse event C1510460 Orofaciodigital syndrome i MalaCards|HPO C0009806 Constipate C0000833 Abscess HSDN C1069915 Vertigo C0032268 Pneumocephalus HSDN C4084802 Usual severity diarrhea C0004030 Aspergillosis HSDN C0424755 Fever symptoms C0948264 Neuroborreliosis MalaCards C0231528 Muscle pain generalized C0543697 Mixed cryoglobulinemia OrphaNet|MalaCards C0349506 Sun sensitivity C0009207 Cockayne syndrome OrphaNet|MalaCards C0032617 High urine output C0236969 Substance-related disorders HSDN C1519353 Skin eruption papular C2745948 Hyalinosis, systemic MalaCards C0015469 Facial paralysis C3150415 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 MalaCards|HPO C1961131 Cough adverse event C0010356 Cross infection HSDN C0242936 Center pain C0151699 Intracranial hemorrhages HSDN C4084769 Vomiting frequency C0003486 Aortic aneurysm HSDN C0036572 Convulsion C1555865 Forensic psychiatry HSDN C1260880 Nasal drip C0028432 Nose diseases UMLS C0231835 Respiration rate increased C0018915 Hemangioendothelioma HSDN C0013421 Dystonia C0338473 Neuroaxonal dystrophies HSDN C4085661 Usual severity nausea C0003486 Aortic aneurysm HSDN C3829611 Nausea frequency C0344315 Depressed mood HSDN C2911645 Weight loss adverse event C0029396 Heterotopic ossification HSDN C4085210 Usual severity pain C0041188 Pyomyositis, tropical HSDN C0009460 Communication impairment C0033906 Psychological theories HSDN C0427055 Face weakness C0270952 Muscular dystrophy, oculopharyngeal MalaCards|HPO|UMLS C0085636 Light sensitivity C0342684 Ocular albinism, type i OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0021845 Intestinal perforation HSDN C1268578 Palatal paresis C0853240 Mobius ii syndrome MalaCards C1963184 Nystagmus adverse event C1849088 Spinocerebellar ataxia with dysmorphism OrphaNet C4085642 Level of joint stiffness C1848650 Ulnar hypoplasia with mental retardation MalaCards C3539889 Pelvic pain increasing in severity C1547940 Specimen source codes - ulcer HSDN C0018784 Deafness sensorineural C1866095 Deafness, autosomal dominant 13 MalaCards|HPO C0016199 Pain flank C1272677 Benign mixed epithelial and stromal tumor of kidney UMLS C0040264 Ear ringing sound C0003486 Aortic aneurysm HSDN C0004604 Pain back C2117118 X-ray of toe: deformity contracture HSDN C1961131 Cough adverse event C0016045 Fibroma HSDN C0151686 Growth retardation C0342195 Thyroid dyshormonogenesis 4 MalaCards|HPO C0013404 Respiratory difficulty C0011127 Pressure ulcer HSDN C4085548 Usual severity dizziness C0023267 Fibroid tumor HSDN C0030486 Extremity paralysis, lower C0206366 Ossification of posterior longitudinal ligament HSDN C1963137 Hydrocephalus adverse event C0011265 Presenile dementia MalaCards C0037763 Spasm C0013289 Duodenal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036285 Scarlet fever HSDN C0024031 Back pain lower back C0029410 Osteoarthritis of hip HSDN C0018989 Paresis of one side of body C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C2984058 Have pain C0022882 Infection laboratory HSDN C0027497 Queasy C0012691 Dislocations HSDN C0004604 Pain back C0033968 Psychotherapeutic technique HSDN C0232513 Premature tooth loss C1843042 Craniolenticulosutural dysplasia OrphaNet|HPO|MalaCards C0085636 Light sensitivity C1835865 Cone-rod dystrophy 11 MalaCards|HPO C1557397 Adverse event associated with pain C1704212 Embolism embolus HSDN C0011991 Loose stools C0524909 Hepatitis b, chronic HSDN C0858908 Eyes heavy feeling of C0004095 Asthenopia UMLS C0027796 Neuralgias C0027814 Neuritis, autoimmune, experimental HSDN C4085222 Nausea C0007125 Carcinoma, ehrlich tumor HSDN C0700078 Deep tendon reflex decrease C0007965 Chediak-higashi syndrome MalaCards|HPO|UMLS C0018524 Hallucinate C0020541 Hypertension, portal HSDN C0013390 Cramps menstrual C0008732 Chylous ascites HSDN C0018991 Paralysis one side of body C0020225 Hydranencephaly HSDN C0039870 Leanness C0039006 Swine--diseases HSDN C0018989 Paresis of one side of body C0022661 Kidney failure, chronic UMLS C4084726 Distress cough C0036117 Salmonella infections HSDN C0009806 Constipate C4225274 Au-kline syndrome UMLS C4084775 Usual severity weight loss C0011633 Dermatomyositis OrphaNet|HSDN|MalaCards C0042024 Urine incontinence C0010823 Cytomegalovirus infections HSDN C0424755 Fever symptoms C0276241 Malignant catarrhal fever HSDN C0021359 Infertility C1867858 Prader-willi syndrome chromosome region HPO C0020458 Hyperhydrosis C1850568 Nakajo syndrome MalaCards C1963087 Constipation adverse event C0795841 Jacobsen distal 11q deletion syndrome OrphaNet|HPO|MalaCards C1963086 Confusion adverse event C1263846 Attention deficit hyperactivity disorder HSDN C0041657 Consciousness loss C0037188 Sinoatrial block HSDN C3815497 Cough C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3641756 Have diarrhea C1962974 Chylothorax adverse event HSDN C4084727 Cough frequency C0009240 Cognition HSDN C0011168 Disorder deglutition C2750069 Lipodystrophy, congenital generalized, type 4 OrphaNet|HPO|MalaCards C4049602 Hyperactivity C0431399 Familial aplasia of the vermis MalaCards|HPO C4042891 Sleep wake disorders C0700201 Dyssomnias HSDN C0007758 Cerebellar ataxia C1859567 Bardet-biedl syndrome 9 HPO C0030486 Extremity paralysis, lower C0038395 Streptococcal infections HSDN C4084766 Vomiting C0852654 21-hydroxylase deficiency MalaCards C1999266 Depression adverse event C2936779 Hydroxymethylbilane synthase deficiency MalaCards C1963252 Tremor adverse event C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C3203358 Alveolar hypoventilation C0270932 Neuropathy paraneoplastic HSDN C4084774 Have weight loss C2931785 Juvenile dermatomyositis MalaCards C2919142 Short stature adverse event C3501846 Noonan-like syndrome with loose anagen hair OrphaNet|HPO C0013404 Respiratory difficulty C0854986 Lung adenocarcinoma stage ii UMLS C3539889 Pelvic pain increasing in severity C0037072 Diseases sigmoid HSDN C0009676 Confusion state C1865323 Migraine, familial basilar HPO C0522224 Palsied C0015663 Fasting HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035228 Respiratory hypersensitivity HSDN C1557397 Adverse event associated with pain C0037313 Sleep HSDN C1963093 Dizziness adverse event C2240374 Eosinophil count raised HSDN C0000737 Abdomen pain C0021799 Interprofessional relations HSDN C3641756 Have diarrhea C0024894 Mastitis HSDN C0018834 Brash C1290138 Ssc without skin involvement MalaCards C0000737 Abdomen pain C2987160 Mixed acinar-ductal carcinoma of the pancreas UMLS C3665347 Vision impaired C0346373 Malignant melanoma of iris OrphaNet|HPO C0009421 Comatose C0017636 Glioblastoma HSDN C4085210 Usual severity pain C0854912 Pineal germinoma HSDN C0042571 Vertigo subjective C0018939 Hematological disease HSDN C0011570 Monopolar depression C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C0002962 Angina C0026636 Mouth diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0042900 Vitiligo HSDN C0086437 Joint hypermobility C2930970 Acromesomelic dysplasia hunter-thompson type MalaCards C0015468 Face pain C1830398 Grooming:-:point in time:^patient:- HSDN C0917816 Deficiency mental C4012050 Hennekam lymphangiectasia-lymphedema syndrome 1 MalaCards C4084802 Usual severity diarrhea C0007020 Carbon monoxide poisoning HSDN C2203646 Jaundice C0014347 Enterobacteriaceae infections HSDN C0151827 Pain eye C0017612 Glaucoma, open-angle HSDN C0032617 High urine output C1563706 Nephrogenic diabetes insipidus, type ii HPO|UMLS C4084784 Diarrhea C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0042571 Vertigo subjective C0702221 Tactual discrimination HSDN C2919142 Short stature adverse event C1852513 Coxoauricular syndrome OrphaNet|MalaCards C2032396 Pelvic pain on the right C0033578 Prostatic neoplasms HSDN C0036572 Convulsion C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C0036572 Convulsion C3897742 Recurrent childhood subependymal giant cell astrocytoma UMLS C1961131 Cough adverse event C0037355 Smallpox vaccines HSDN C4084725 Usual severity cough C1956089 Osteophyte HSDN C0042963 Symptoms vomiting C0022665 Kidney neoplasm HSDN C3641756 Have diarrhea C1000587 Pemphigus HSDN C3463815 Feel fatigue C1963084 Colitis adverse event HSDN C0003550 Broca aphasia C0012746 Dissociative disorder HSDN C0036572 Convulsion C0015397 Disorder of eye HSDN C4084769 Vomiting frequency C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0018784 Deafness sensorineural C0034069 Pulmonary fibrosis HSDN C0043094 Weight gain C0007099 Carcinoma in situ HSDN C4084769 Vomiting frequency C0001973 Alcoholic intoxication, chronic HSDN C1263846 Attention deficit disorder with hyperactivity C3150928 Nf1 microdeletion syndrome MalaCards C1557397 Adverse event associated with pain C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0020903 Illusion C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0011570 Monopolar depression C1963674 Spinocerebellar ataxia 10 MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0013274 Patent ductus arteriosus HSDN C0034150 Skin purpura C1999266 Depression adverse event HSDN C4085549 Dizziness C0520679 Sleep apnea, obstructive HSDN C0010200 Cough symptom C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C1384666 Decreased hearing C0796561 Melanoma vaccines HSDN C0032617 High urine output C0024473 Magnesium deficiency HSDN C1549543 Administration method - pain C0032994 Pregnancy, tubal HSDN C0036659 Sensation disorder C0034735 Raynaud phenomenon HSDN C4084776 Weight loss C0032371 Poliomyelitis HSDN C2126105 Medial left leg soft tissue swelling C0037580 Soft tissue swelling UMLS C0004134 Dyssynergia C0017675 Glossitis HSDN C4085548 Usual severity dizziness C0033893 Tension headache HSDN C1565249 Limitation, mobility C0003811 Cardiac arrhythmia HSDN C0424755 Fever symptoms C0018552 Hamartoma HSDN C0424755 Fever symptoms C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C0085128 Cardiac output elevated C0035410 Rhabdomyolysis HSDN C1557397 Adverse event associated with pain C0019322 Umbilical hernia HSDN C0042024 Urine incontinence C2240374 Eosinophil count raised HSDN C1963071 Back pain adverse event C0021359 Infertility HSDN C0020615 Hypoglycemia nos C3554606 Mc3dn3 MalaCards C0030193 Sense of pain C0812470 Abortion, incomplete HSDN C0003862 Pain joint C0037397 Behavior social HSDN C0036572 Convulsion C2931788 Atypical hemolytic uremic syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0042974 Von willebrand disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0162703 Pain sensitivity HSDN C2024878 Cardiovascular surgery result: dyspnea C3494506 Pseudohypoparathyroidism, type ia HPO C0375546 Heart murmur undiagnosed C0810277 Other heart valve disorders UMLS C0015468 Face pain C0039984 Thoracic outlet syndrome HSDN C4084724 Usual severity constipation C0018802 Congestive heart failure HSDN C3541349 Syncope C1963064 Anxiety adverse event HSDN C1963077 Bone pain adverse event C0024454 Maffucci syndrome OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0005967 Bone neoplasms HSDN C0018772 Deafness C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C3829611 Nausea frequency C0026640 Mouth neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010481 Cushing syndrome HSDN C0004604 Pain back C0023860 Listeriosis DiseaseOntology|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0020305 Fetal edema C1253937 Pericardial effusion HSDN C0917816 Deficiency mental C3809853 Mental retardation, autosomal recessive 39 MalaCards C4085222 Nausea C0677866 Brain stem neoplasms HSDN C0424755 Fever symptoms C0040361 Togaviridae infections HSDN C0241700 Voice fatigue C1868594 Perry syndrome MalaCards|HPO C3665492 Pigmentations C1335302 Pancreatic ductal adenocarcinoma MalaCards C2364111 Gustatory anesthesia C0018674 Head trauma HSDN C0013421 Dystonia C2931919 X-linked infantile spasm syndrome MalaCards|HPO C0042963 Symptoms vomiting C0008313 Cholangitis, sclerosing UMLS C4084726 Distress cough C0009917 Contracture HSDN C0018772 Deafness C0024689 Mandibular diseases HSDN C2237041 Shox gene with short stature C2931270 Craniodiaphyseal dysplasia, dominant MalaCards C0007758 Cerebellar ataxia C0005967 Bone neoplasms HSDN C3665492 Pigmentations C0206710 Basal cell neoplasm MalaCards C0150055 Pain chronic C0033873 Psychiatry HSDN C0018772 Deafness C0014236 Endophthalmitis HSDN C0028738 Nystagmus C1859567 Bardet-biedl syndrome 9 HPO C1963249 Tinnitus adverse event C0010346 Crohn disease HSDN C0018991 Paralysis one side of body C0024636 Malocclusion HSDN C0036659 Sensation disorder C0011849 Diabetes mellitus HSDN C3815497 Cough C0014461 Granuloma eosinophilic MalaCards C0042384 Vasculitis, nonspecific C2931873 Juvenile cranial arteritis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0398623 Thrombophilia HSDN C0013395 Indigestion C0848377 Trauma to the abdomen HSDN C0242936 Center pain C0038436 Post-traumatic stress disorder HSDN C0231528 Muscle pain generalized C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C4085549 Dizziness C0018916 Hemangioma HSDN C0018681 Headache, cephalalgia C0017160 Gastroenteritis HSDN C0019825 Voice hoarseness C0919267 Ovarian neoplasm HSDN C4084775 Usual severity weight loss C0016952 Galactosemias MalaCards C0018772 Deafness C2931347 Cardiac form of generalized glycogenosis MalaCards|HPO C0233514 Behavior abnormal C0238286 Mucolipidosis type iv OrphaNet|MalaCards C0426579 Anorexia symptom C0272414 Displaced spleen HSDN C2024893 Cardiovascular surgery result: fatigue C0035127 Cumulative trauma disorders HSDN C0038990 Sweats C0029411 Osteoarthropathy, primary hypertrophic MalaCards|HPO C0028738 Nystagmus C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C3887638 Failure to thrive in infant C0340951 Erythrogenesis imperfecta MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0001815 Primary myelofibrosis HSDN C0424755 Fever symptoms C1861751 Minicore myopathy, moderate, with hand involvement HPO C0036396 Sciatica C0684743 Malignant neoplasm of muscle HSDN C0020578 Hyperventilate C0085682 Hypophosphatemia HSDN C3898969 Have been vomiting C0017152 Gastritis HSDN C2029884 Hearing loss by exam C0016508 Congenital foot deformity HSDN C0398650 Idiopathic thrombocytopenia purpura C0022658 Kidney diseases HSDN C0413252 Hypothermia due to exposure C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0026858 Musculoskeletal pain C1963138 Hypertension adverse event HSDN C4084769 Vomiting frequency C0017638 Glioma HSDN C0349588 Stature short C3891452 Seckel syndrome 8 MalaCards C0018772 Deafness C0033923 Psychomotor function HSDN C0041657 Consciousness loss C0011849 Diabetes mellitus HSDN C3665347 Vision impaired C1857277 Donnai-barrow syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C0015674 Chronic fatigue syndrome HSDN C0018784 Deafness sensorineural C2750090 Charcot-marie-tooth disease, axonal, type 2n MalaCards C4085549 Dizziness C0010068 Coronary heart disease HSDN C0026205 Pupillary constriction C0022073 Iridocyclitis HSDN C0012569 Double vision C1832855 Choreoathetosis/spasticity, episodic MalaCards C0398650 Idiopathic thrombocytopenia purpura C0752143 Intracranial thrombosis HSDN C0034933 Abnormal reflexes C1000483 Genus anemia HSDN C0011570 Monopolar depression C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C0020305 Fetal edema C0206620 Lymphangioma, cystic MalaCards C0221758 Back stiffness C0038013 Ankylosing spondylitis MalaCards C0032617 High urine output C0043352 Xerostomia HSDN C3641755 Have constipation C3887532 Ulceration HSDN C4084773 Bothered by weight gain C0023473 Myeloid leukemia, chronic HSDN C4085222 Nausea C0007760 Cerebellar diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001163 Vestibulocochlear nerve diseases HSDN C1557397 Adverse event associated with pain C0024954 Maxillary neoplasms HSDN C4085548 Usual severity dizziness C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0019209 Large liver C1837028 Severe combined immunodeficiency, autosomal recessive, t cell negative, b cell positive, nk cell positive HPO C0015469 Facial paralysis C1864668 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4 MalaCards|HPO C0086437 Joint hypermobility C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C0004134 Dyssynergia C0001125 Acidosis, lactic HSDN C1527344 Dysphonia C1963138 Hypertension adverse event HSDN C0009806 Constipate C0039980 Chest injury HSDN C0005745 Blepharoptosis C1848912 Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage MalaCards C3665492 Pigmentations C0027830 Neurofibroma MalaCards C0476273 Distress respiratory C1334683 Endodermal sinus neoplasm of mediastinum UMLS C0151786 Weakness muscle C0860603 Anxiety symptoms HSDN C0473240 Dipstix hematuria C1282054 Hematuria of undiagnosed cause UMLS C2911647 Weight gain adverse event C0026640 Mouth neoplasms HSDN C0751495 Seizure focal C0234533 Generalized seizures UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0078981 Arachnoid cysts HSDN C0020615 Hypoglycemia nos C1857355 Leigh syndrome , french canadian type HPO C0007758 Cerebellar ataxia C0687751 Acanthocytosis MalaCards C1549543 Administration method - pain C0031941 Pineal gland neoplasm HSDN C4084775 Usual severity weight loss C0243057 Stomatognathic system abnormalities HSDN C1999266 Depression adverse event C2930815 Acute cerebral gaucher disease MalaCards C1962956 Flatulence adverse event C0034885 Rectal neoplasms HSDN C0004604 Pain back C0004626 Pneumonia, bacterial HSDN C0041657 Consciousness loss C0020649 Hypotension HSDN C0233794 Memory impaired C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0013404 Respiratory difficulty C0041956 Ureteral obstruction HSDN C0349506 Sun sensitivity C0011633 Dermatomyositis MalaCards C0009676 Confusion state C0003873 Rheumatoid arthritis HSDN C2911647 Weight gain adverse event C0032227 Pleural effusion disorder HSDN C0030552 Paralysis partial C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C4084725 Usual severity cough C1401747 Quadrilateral fever MalaCards C0595939 Stillborn C0265274 Achondrogenesis, type ib (disorder) HPO C0030486 Extremity paralysis, lower C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0033860 Psoriasis HSDN C2984057 Have nausea C0020544 Renal hypertension HSDN C0018784 Deafness sensorineural C2931369 Hearing loss and familial salivary gland insensitivity to aldosterone OrphaNet|MalaCards C0522224 Palsied C0035126 Reperfusion injury HSDN C4085862 Bothered by nausea C1302282 Chromaffin cell neoplasm MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0006271 Bronchiolitis HSDN C2237041 Shox gene with short stature C0796003 Juberg-marsidi syndrome HPO C0454644 Delayed language development C1970848 Phosphoglycerate kinase 1 deficiency MalaCards|HPO C0037763 Spasm C3808991 Congenital disorder of deglycosylation MalaCards C0002170 Alopecia disorders C1970140 Aplasia cutis congenita, congenital heart defect, and frontonasal cysts HPO C3146279 Coma C0004161 Athletic injuries HSDN C1963091 Diarrhea adverse event C0006271 Bronchiolitis HSDN C0917816 Deficiency mental C3489787 Pituitary hormone deficiency, combined, 3 MalaCards C0042024 Urine incontinence C0016542 Foreign body HSDN C4084769 Vomiting frequency C0002994 Angioedema HSDN C0030794 Pelvis pain C1552262 Nurse practitioner - family HSDN C0020672 Body temperature decreased C0403447 Chronic kidney insufficiency HSDN C0040264 Ear ringing sound C0349604 Intracranial meningioma MalaCards C1963167 Memory impairment adverse event C2931918 Transketolase defect MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0342649 Vascular calcification HSDN C0034150 Skin purpura C0017567 Gingival hypertrophy HSDN C0241210 Speaking delay C1414025 Dgcr gene HPO C0007166 Cardiac output decreased C0003873 Rheumatoid arthritis HSDN C3463815 Feel fatigue C3463824 Myelodysplastic syndrome HSDN C0042571 Vertigo subjective C0020676 Hypothyroidism HSDN C4084774 Have weight loss C0037944 Spinal stenosis HSDN C0270777 Cord edema spinal C0474992 Edema of thoracic cord UMLS C0750426 Wbc elevated C0023473 Myeloid leukemia, chronic OrphaNet|HPO C0040822 D tremors C0004623 Bacterial infections HSDN C0026826 High muscle tone C2750536 Nemaline myopathy 3, with intranuclear rods HPO C2237041 Shox gene with short stature C0796117 Pitt syndrome MalaCards C0004941 Behavioral symptoms C0814154 Alcohol-related neurodevelopmental disorder OrphaNet|MalaCards C4084724 Usual severity constipation C0024115 Lung diseases HSDN C4084773 Bothered by weight gain C0019699 Hiv seropositivity HSDN C4084784 Diarrhea C0162871 Aortic aneurysm, abdominal HSDN C0006370 Bulimia C2984299 Asthma pathway HSDN C0023380 Lethargy C0001125 Acidosis, lactic HSDN C0042571 Vertigo subjective C0038358 Gastric ulcer HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0037355 Smallpox vaccines HSDN C0030193 Sense of pain C0002989 Epithelioid hemangioma of skin HSDN C4085661 Usual severity nausea C0023220 Leg injury HSDN C0030193 Sense of pain C0266015 Congenital digestive system anomalies HSDN C4085210 Usual severity pain C0037005 Shoulder dislocation HSDN C1557397 Adverse event associated with pain C0027719 Nephrosclerosis HSDN C1963184 Nystagmus adverse event C0268496 Kramer syndrome OrphaNet|MalaCards C1963167 Memory impairment adverse event C1836383 Spinocerebellar ataxia 27 HPO C0030552 Paralysis partial C2609414 Acute kidney injury HSDN C0011991 Loose stools C0014591 Epistaxis HSDN C0043094 Weight gain C0003467 Anxiety HSDN C4085210 Usual severity pain C0019066 Nontraumatic hemoperitoneum HSDN C1384666 Decreased hearing C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C0002871 Anemia HSDN C2919142 Short stature adverse event C1850338 Oculopalatocerebral syndrome MalaCards C3539891 Pelvic pain to the rear C0021831 Intestinal diseases HSDN C0014724 Burping C0009946 Conversion disorder HSDN C4085317 Diarrhea frequency C1829813 Malonic acidemia MalaCards C0237326 Defecation pain C0342191 Familial dyshormonogenetic goiter MalaCards C1963184 Nystagmus adverse event C2931121 Meier blumberg imahorn syndrome OrphaNet|HPO|MalaCards C0003079 Pupillary inequality C0013592 Ectropion HSDN C4084723 Constipation C3241945 Melena due to gastrointestinal hemorrhage HSDN C0018772 Deafness C0035579 Rickets HSDN C1557397 Adverse event associated with pain C0028879 Odontogenic cysts HSDN C3146279 Coma C0025294 Meningococcal meningitis HSDN C0151686 Growth retardation C3150971 Leopard syndrome 3 MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0015672 Decreased energy C1457883 Aggressive reaction HSDN C0009676 Confusion state C3542426 Inferior myocardial infarction by ecg finding HSDN C0010200 Cough symptom C1710173 Squamous cell lung carcinoma, basaloid variant UMLS C0231791 In toe C2713347 7-dehydrocholesterol reductase deficiency MalaCards C0344435 Ventricular fibrillation by ecg finding C2673193 Brugada syndrome 2 MalaCards|HPO C0026205 Pupillary constriction C0040997 Trigeminal neuralgia HSDN C0027796 Neuralgias C0011265 Presenile dementia HSDN C1962972 Proteinuria adverse event C0006264 Bronchial neoplasms HSDN C0557874 Global developmental delay C2749019 Joubert syndrome 10 (disorder) MalaCards C4085210 Usual severity pain C0038644 Sudden infant death syndrome HSDN C0020505 Excessive eating C1269683 Major depressive disorder HSDN C4084766 Vomiting C1009209 Tinea HSDN C0151786 Weakness muscle C2713447 Hyperpotassemia and hypertension, familial MalaCards C0085593 Chill C0744968 Hiv fever UMLS C1963281 Vomiting adverse event C1706377 Memory device component HSDN C0039070 Collapse fleeting C0007282 Carotid stenosis HSDN C1963093 Dizziness adverse event C0004245 Atrioventricular block HSDN C0018772 Deafness C0016169 Pathologic fistula HSDN C0518090 Frequency of pain question C0036285 Scarlet fever HSDN C1557397 Adverse event associated with pain C0017168 Gastroesophageal reflux disease HSDN C4084766 Vomiting C0409959 Osteoarthritis, knee HSDN C1557397 Adverse event associated with pain C0042384 Vasculitis HSDN C0019079 Bloody sputum C0022116 Ischemia HSDN C1557397 Adverse event associated with pain C0031030 Periapical periodontitis HSDN C0030552 Paralysis partial C0268328 Porphobilinogen synthase deficiency MalaCards C0522224 Palsied C1547044 Kind of quantity - smell HSDN C0497406 Over weight C4049644 Depression HSDN C1963091 Diarrhea adverse event C0026896 Myasthenia gravis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013182 Drug allergy HSDN C2919142 Short stature adverse event C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C0007758 Cerebellar ataxia C3150730 Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency HPO C4085210 Usual severity pain C1504665 Products used to treat diabetic ketoacidosis HSDN C0917816 Deficiency mental C1858516 Microcephaly 4, primary, autosomal recessive MalaCards|HPO C1963281 Vomiting adverse event C0023374 Lesch-nyhan syndrome MalaCards|HPO C4085642 Level of joint stiffness C4024957 Proximal spinal muscular atrophy MalaCards C0917816 Deficiency mental C0392475 Roberts-sc phocomelia syndrome OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0268543 Hyperammonemia, type iii MalaCards C1145670 Failure respiratory C1835555 Larynx, congenital partial atresia of OrphaNet|MalaCards C4085210 Usual severity pain C0376547 Aromatherapy HSDN C4084774 Have weight loss C1509147 Histiocytoma HSDN C4085210 Usual severity pain C0009062 Clostridia infection HSDN C3898969 Have been vomiting C2004491 Cicatrix HSDN C0011175 Deficient fluid volume C0022810 Disease, kyasanur forest MalaCards C1145670 Failure respiratory C0021368 Inflammation MalaCards C0040460 Dental pain C0149931 Migraine disorders HSDN C0018772 Deafness C0752180 Bacterial cns infection HSDN C3539889 Pelvic pain increasing in severity C0041582 Ulcer HSDN C0162834 Hyperpigmentation C0008312 Primary biliary cirrhosis OrphaNet|HPO|MalaCards C0013395 Indigestion C0344435 Ventricular fibrillation by ecg finding HSDN C0042024 Urine incontinence C0002792 Anaphylaxis HSDN C2237041 Shox gene with short stature C0020557 Hypertriglyceridemia MalaCards C0700590 Diaphoresis excessive C0017075 Ganglioneuroma MalaCards C0013132 Drooling C3713418 Ppm-x syndrome MalaCards C0013604 Edematous C0042580 Vesico-ureteral reflux HSDN C0022346 Yellow skin C0001144 Acne vulgaris HSDN C4085222 Nausea C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0020505 Excessive eating C0003873 Rheumatoid arthritis HSDN C4084774 Have weight loss C0016045 Fibroma HSDN C3665347 Vision impaired C1850055 Peho syndrome OrphaNet|HPO|MalaCards C3898969 Have been vomiting C0268151 Classical galactosemia MalaCards|HPO C0042755 Virilisation C0025521 Inborn errors of metabolism HSDN C1000483 Genus anemia C0023903 Liver neoplasms MalaCards C0030193 Sense of pain C0005283 Beta thalassemia HSDN C1549543 Administration method - pain C4042784 Feeding and eating disorders HSDN C2237041 Shox gene with short stature C0268338 Ehlers-danlos syndrome, type iv OrphaNet|HPO C3887638 Failure to thrive in infant C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C3827868 Tachycardia by ecg finding HSDN C0013608 Cardiac edema C0020428 Hyperaldosteronism HSDN C2911645 Weight loss adverse event C1510415 Osteosclerotic myeloma MalaCards C0020615 Hypoglycemia nos C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0042798 Vision dim C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C0036572 Convulsion C3887877 Deficiency of glycerate kinase MalaCards C0917816 Deficiency mental C0349655 Congenital disorder of glycosylation, type i-iix MalaCards C4085211 Pain distress question C0002448 Ameloblastoma HSDN C0035232 Diaphragmatic paralysis C0428953 Ecg infarction myocardial HSDN C0034150 Skin purpura C0042880 Vitamin k deficiency HSDN C0393759 Transient insomnia C0154566 Transient disorder of initiating or maintaining sleep UMLS C3898969 Have been vomiting C0085423 Gram-negative bacterial infections HSDN C0011991 Loose stools C1739094 Foodborne botulism OrphaNet|MalaCards C0007398 Catatonic C0014548 Epilepsy, generalized HSDN C0027498 Nausea vomiting C0267797 Acute hepatitis UMLS C3887873 Hearing loss C0812393 Cancer patients and suicide and depression HSDN C4085317 Diarrhea frequency C1956257 Pulmonary stenosis HSDN C0002965 Crescendo angina C0023530 Leukopenia HSDN C4084775 Usual severity weight loss C0079487 Helicobacter infections HSDN C0086565 Liver function abnormal C1837396 Congenital disorder of glycosylation, type ie MalaCards|HPO C4085211 Pain distress question C0036285 Scarlet fever HSDN C0151908 Dry skin C2936859 N syndrome MalaCards C1971624 Appetite absent C0270858 Abdominal migraines MalaCards C0011991 Loose stools C1833275 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0006849 Oral candidiasis HSDN C3274924 Have been coughing C0037397 Behavior social HSDN C4084775 Usual severity weight loss C0000809 Abortion, habitual HSDN C0028738 Nystagmus C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards|HPO C0812426 Kidney problem C0035067 Renal artery stenosis UMLS C3829611 Nausea frequency C0027831 Neurofibromatosis 1 HSDN C0015230 Exanthem C0032285 Pneumonia UMLS C4084767 Bothered by vomiting C2945767 Childhood liver cancer MalaCards C0042963 Symptoms vomiting C1332972 Childhood infratentorial ependymoblastoma UMLS C4084767 Bothered by vomiting C0919267 Ovarian neoplasm HSDN C2919142 Short stature adverse event C3280616 Cranioectodermal dysplasia 4 MalaCards C0233565 Bradykinesia C2750442 Hypermanganesemia with dystonia polycythemia and cirrhosis HPO|UMLS C1549543 Administration method - pain C0004245 Atrioventricular block HSDN C1549543 Administration method - pain C0041107 Trisomy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001969 Alcoholic intoxication HSDN C0013395 Indigestion C0004096 Asthma HSDN C1557397 Adverse event associated with pain C0233315 Premature birth of newborn HSDN C0027497 Queasy C0003493 Aortic diseases HSDN C0085631 Abnormal excitement C2609414 Acute kidney injury HSDN C0018784 Deafness sensorineural C0029896 Disease, ent HSDN C0009806 Constipate C0033975 Psychotic disorders HSDN C0036572 Convulsion C0010246 Coxsackievirus infections HSDN C0003862 Pain joint C1846843 Epiphyseal dysplasia, multiple, 5 OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0022665 Kidney neoplasm HSDN C0013604 Edematous C2937358 Cerebral hemorrhage HSDN C0518090 Frequency of pain question C0003486 Aortic aneurysm HSDN C4084726 Distress cough C0085073 Prosthesis-related infection HSDN C4084723 Constipation C0035934 Rubinstein-taybi syndrome OrphaNet|HPO|MalaCards C0015672 Decreased energy C0032927 Precancerous conditions HSDN C2984057 Have nausea C2945560 Hemolytic HSDN C3539023 Pelvic pain increasing in frequency C0006663 Calcinosis HSDN C3463815 Feel fatigue C0040034 Thrombocytopenia HSDN C0917816 Deficiency mental C1835794 Kallmann syndrome 2 with bimanual synkinesia HPO C0013362 Dysarthrias C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards C1260880 Nasal drip C1333477 Ethmoid sinus squamous cell carcinoma UMLS C0917816 Deficiency mental C3275460 Mental retardation, x-linked, syndromic 17 MalaCards C0009676 Confusion state C0014060 Encephalitis, st. louis DiseaseOntology|MalaCards C4084769 Vomiting frequency C0751161 Udpglucose 4-epimerase deficiency disease MalaCards|HPO C3694918 Difficulty swallowing sudden unexplained change C0011168 Deglutition disorders UMLS C3829611 Nausea frequency C0344434 Atrial fibrillation ecg HSDN C0018772 Deafness C1414017 Deafness, autosomal recessive 25 MalaCards|HPO C0011168 Disorder deglutition C1846582 Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration HPO C0006370 Bulimia C0027051 Myocardial infarction HSDN C1963091 Diarrhea adverse event C0035613 Rift valley fever OrphaNet|MalaCards C4084776 Weight loss C0243057 Stomatognathic system abnormalities HSDN C0522224 Palsied C0008519 Ectopic tissue HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0431109 Choroid plexus carcinoma HPO C0033774 Skin pruritus C0406673 Perineal itch syndrome UMLS C0004604 Pain back C0024530 Malaria HSDN C3812171 Bradycardia by ecg finding C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C0413252 Hypothermia due to exposure C0032965 Pregnancy complications, infectious HSDN C2024893 Cardiovascular surgery result: fatigue C0343755 Hiv wasting syndrome HSDN C4085661 Usual severity nausea C0014121 Bacterial endocarditis HSDN C0151786 Weakness muscle C0342643 Autosomal recessive hypophosphatemic vitamin d refractory rickets MalaCards C0043352 Absent salivary secretion C1836122 Sarcoidosis, early-onset MalaCards C0011991 Loose stools C0011269 Dementia, vascular HSDN C0086565 Liver function abnormal C0795969 Cholestasis-pigmentary retinopathy-cleft palate syndrome MalaCards C0011991 Loose stools C0014859 Esophageal neoplasms HSDN C0018991 Paralysis one side of body C0018024 Goiter, retrosternal HSDN C4085211 Pain distress question C0043254 Injuries penetrating HSDN C2032396 Pelvic pain on the right C1547940 Specimen source codes - ulcer HSDN C3463815 Feel fatigue C0001546 Adjustment disorders HSDN C0012833 Dizzy C0002989 Epithelioid hemangioma of skin HSDN C1961131 Cough adverse event C1455705 Pulmonary histiocytosis x OrphaNet|MalaCards C4084773 Bothered by weight gain C1258104 Diffuse scleroderma HSDN C4084768 Usual severity vomiting C0740392 Infarction, middle cerebral artery HSDN C1962972 Proteinuria adverse event C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C4084727 Cough frequency C0019080 Hemorrhage HSDN C0002622 Amnesias C0001849 Aids dementia complex HSDN C0033377 Caudal displacement C1861178 Thrombocytopenia paris-trousseau type MalaCards C0004093 Asthenia C0040053 Thrombosis HSDN C0576456 Poor feeding C1850055 Peho syndrome MalaCards C4084773 Bothered by weight gain C0017638 Glioma HSDN C0012833 Dizzy C0007781 Intracranial embolism and thrombosis HSDN C0155552 Hearing loss mixed C1855607 Keutel syndrome MalaCards C4084768 Usual severity vomiting C0027121 Myositis HSDN C0043094 Weight gain C0034089 Pulmonary valve stenosis HSDN C3898969 Have been vomiting C0042373 Vascular diseases HSDN C0231791 In toe C1857576 Contractures, congenital, torticollis, and malignant hyperthermia MalaCards C0011991 Loose stools C0856761 Budd-chiari syndrome HSDN C4085661 Usual severity nausea C0027092 Myopia HSDN C0231528 Muscle pain generalized C0268123 Muscle amp deaminase deficiency MalaCards C1963249 Tinnitus adverse event C1999266 Depression adverse event HSDN C3541349 Syncope C0026590 Child mother relationship HSDN C4084726 Distress cough C0006271 Bronchiolitis MalaCards C0018681 Headache, cephalalgia C0026771 Trauma multiple HSDN C0557874 Global developmental delay C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C0016204 Fart C1548578 Location characteristic id - smoking HSDN C0860603 Anxiety symptom C2931859 Acquired cjd MalaCards C0020615 Hypoglycemia nos C1849821 Phosphoenolpyruvate carboxykinase deficiency, mitochondrial HPO C0036396 Sciatica C0034929 Reflex HSDN C1963137 Hydrocephalus adverse event C0026709 Mucopolysaccharidosis vi MalaCards|HPO C0424755 Fever symptoms C1720777 Functional laterality HSDN C0039070 Collapse fleeting C0033817 Pseudomonas infections HSDN C0015672 Decreased energy C0043195 Subsepsis hyperergia syndrome OrphaNet|MalaCards C0206146 Myocardial stunning C0042510 Ventricular fibrillation HSDN C4084766 Vomiting C4049644 Depression HSDN C0036396 Sciatica C2984289 Melanoma pathway HSDN C2911645 Weight loss adverse event C0220981 Metabolic acidosis HSDN C0015230 Exanthem C0343057 Keratosis pilaris decalvans UMLS C0023380 Lethargy C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C2984057 Have nausea C0038362 Stomatitis HSDN C4084774 Have weight loss C0268151 Classical galactosemia OrphaNet|HPO|MalaCards C0460137 Push down or depress C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C0151786 Weakness muscle C0026266 Mitral valve insufficiency HSDN C0039070 Collapse fleeting C0410189 Muscular dystrophy, emery-dreifuss HSDN C0727671 Red cross toothache drops C0236969 Substance-related disorders HSDN C4084776 Weight loss C0376545 Hematologic neoplasms HSDN C4084726 Distress cough C0007099 Carcinoma in situ HSDN C0020672 Body temperature decreased C0000833 Abscess HSDN C4084776 Weight loss C0242698 Ventricular dysfunction, left HSDN C0011991 Loose stools C0022570 Keratitis dentritic HSDN C0007398 Catatonic C0018946 Hematoma, subdural HSDN C2203646 Jaundice C0268314 Cholestasis-edema syndrome, norwegian type OrphaNet|MalaCards C4084769 Vomiting frequency C0027583 Nematode infections HSDN C0004093 Asthenia C0002871 Anemia HSDN C2911647 Weight gain adverse event C0035459 Atrophic rhinitis HSDN C2315100 Pediatric failure to thrive C0001193 Apert syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0334533 Arteriovenous hemangioma HSDN C0877473 Mouth tight C0043352 Xerostomia UMLS C4049602 Hyperactivity C2931247 Chromosome 17, trisomy 17q22 MalaCards C3539896 Pelvic pain occurs with urination C0021831 Intestinal diseases HSDN C1279888 Proteinuria of undiagnosed cause C2931872 Free sialic acid storage disease MalaCards C0009676 Confusion state C2984572 Malaria pathway HSDN C2984058 Have pain C0029443 Osteomyelitis HSDN C1557397 Adverse event associated with pain C0017662 Glomerulonephritis, membranoproliferative HSDN C0860603 Anxiety symptom C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C0010200 Cough symptom C1565106 Headache disorders, primary HSDN C3539896 Pelvic pain occurs with urination C0034888 Rectal prolapse HSDN C0518090 Frequency of pain question C0008475 Patella chondromalacia HSDN C1579931 Depressed - symptom C0398746 Gluthathione synthetase deficiency MalaCards C4084727 Cough frequency C0238990 Acute lower respiratory tract infection MalaCards C3641756 Have diarrhea C0040409 Tongue diseases HSDN C0497247 Blood pressure elevation C0403556 Glomerulopathy, familial lobular MalaCards C1963065 Apnea adverse event C1546533 Specimen source codes - abscess HSDN C1565249 Limitation, mobility C2911643 Encounter due to family history of osteoporosis HSDN C0026838 Spasticity muscle C0428953 Ecg infarction myocardial HSDN C1999266 Depression adverse event C0795953 Masa syndrome (disorder) MalaCards C1963281 Vomiting adverse event C0002726 Amyloidosis HSDN C0085642 Asphyxia reticularis C0040038 Thromboembolism HSDN C0151889 Reflexes tendon increased C2746067 Spinocerebellar ataxia 22 HPO C0030193 Sense of pain C0162566 Porphyria cutanea tarda HSDN C1963281 Vomiting adverse event C0198632 Pneumoperitoneum HSDN C0030552 Paralysis partial C0282607 Vascular neoplasms HSDN C4042891 Sleep wake disorders C1366622 Mok gene HSDN C0042963 Symptoms vomiting C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0015672 Decreased energy C0002871 Anemia UMLS C0522224 Palsied C0011603 Dermatitis HSDN C2242996 Tingling C1510479 Neuralgic amyotrophy OrphaNet|HPO|MalaCards C0221752 Rbc urine C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C1963091 Diarrhea adverse event C0018915 Hemangioendothelioma HSDN C0020580 Decreased sensation C0019693 Hiv infections HSDN C0015469 Facial paralysis C0024221 Lymphangioma HSDN C0015672 Decreased energy C0014121 Bacterial endocarditis HSDN C4084769 Vomiting frequency C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084769 Vomiting frequency C0348018 Projections HSDN C3641756 Have diarrhea C0151467 Addisonian crisis OrphaNet|MalaCards C0231341 Aging premature C0041948 Uremia HSDN C0030552 Paralysis partial C1547046 Kind of quantity - taste HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032788 Postoperative hemorrhage HSDN C0011168 Disorder deglutition C1837122 Myasthenic syndrome, congenital, fast-channel MalaCards|HPO C0036572 Convulsion C3662840 Partial parietal lobe epilepsy UMLS C4084769 Vomiting frequency C2718092 Acrospiroma HSDN C4084773 Bothered by weight gain C0878544 Cardiomyopathies HSDN C4084723 Constipation C3887992 Thyrotropin-releasing hormone deficiency MalaCards C1962972 Proteinuria adverse event C0039614 Tetanus HSDN C0042024 Urine incontinence C0597109 Nurse's role HSDN C0242936 Center pain C0008495 Chorioamnionitis HSDN C0032617 High urine output C0687720 Central diabetes insipidus MalaCards C2024893 Cardiovascular surgery result: fatigue C1854896 Mucolipidosis iii gamma MalaCards C0018991 Paralysis one side of body C0024115 Lung diseases HSDN C0030200 Intractable pain C0006666 Calciphylaxes HSDN C0349588 Stature short C0020725 Type ii mucolipidosis OrphaNet|HPO|MalaCards C3887638 Failure to thrive in infant C1844696 Otopalatodigital syndrome, type ii OrphaNet|HPO|MalaCards C0018524 Hallucinate C0009953 Convulsive therapy HSDN C1963071 Back pain adverse event C2240374 Eosinophil count raised HSDN C0042024 Urine incontinence C1546654 Specimen source codes - granuloma HSDN C0013362 Dysarthrias C2931441 Hereditary spastic paralysis, infantile onset ascending OrphaNet|HPO|MalaCards C0018524 Hallucinate C0518449 Control of hip fracture risk HSDN C0242936 Center pain C0042376 Vascular headaches HSDN C4085549 Dizziness C0006434 Burn injury HSDN C0008031 Pain chest C1710500 Type ii pleuropulmonary blastoma UMLS C0206146 Myocardial stunning C0003811 Cardiac arrhythmia HSDN C4085317 Diarrhea frequency C0595812 Fistula route HSDN C2315100 Pediatric failure to thrive C3472585 Congenital monosaccharide malabsorption MalaCards C3146279 Coma C0014852 Esophageal diseases HSDN C0015672 Decreased energy C0027092 Myopia HSDN C0026826 High muscle tone C0439840 Reflex motion descriptor HSDN C0042571 Vertigo subjective C0022660 Kidney failure, acute HSDN C0035229 Respiratory function impaired C0018522 Hallermann's syndrome MalaCards C4084788 Have dizziness C0028758 Bonding HSDN C0026884 Muteness C0751706 Primary progressive nonfluent aphasia MalaCards|HPO C0242936 Center pain C0221074 Depression, postpartum HSDN C0424755 Fever symptoms C1704326 Role - roleclass HSDN C0424755 Fever symptoms C2931854 Allergic bronchopulmonary mycosis MalaCards C1557397 Adverse event associated with pain C0376545 Hematologic neoplasms HSDN C0476273 Distress respiratory C0035235 Respiratory syncytial virus infections MalaCards C0426579 Anorexia symptom C0751202 Cystathionine beta-synthase deficiency disease HPO C0242936 Center pain C0038463 Strongyloides infection HSDN C0795692 Lactate blood increased C0018801 Heart failure HSDN C0557874 Global developmental delay C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards C0030975 Disorders perception C0524851 Neurodegenerative disorders HSDN C0010200 Cough symptom C0026771 Trauma multiple HSDN C0018772 Deafness C0037305 Neoplasm, skull HSDN C0015672 Decreased energy C1838280 Epiphyseal dysplasia, multiple, 1 MalaCards C2984058 Have pain C1636667 Disorder characterized by eosinophilia HSDN C0018834 Brash C1845235 Heterotopia, periventricular, ehlers-danlos variant OrphaNet|HPO C0557874 Global developmental delay C2931141 Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency MalaCards|HPO C0039070 Collapse fleeting C0242231 Coronary stenosis HSDN C0424755 Fever symptoms C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C3539893 Pelvic pain occurs with intercourse C0243001 Abdominal abscess HSDN C0000737 Abdomen pain C0011881 Diabetic nephropathy HSDN C0009676 Confusion state C0314657 Genetic predisposition HSDN C0009806 Constipate C0403555 Ochoa syndrome OrphaNet|HPO|MalaCards C0016199 Pain flank C1333841 Grade 3 clear cell renal cell carcinoma UMLS C0018520 Breath odor C0021833 Intestinal fistula HSDN C0002622 Amnesias C0036421 Systemic scleroderma HSDN C1557397 Adverse event associated with pain C0860239 Catheter infections related HSDN C1963281 Vomiting adverse event C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO C0030193 Sense of pain C0039585 Androgen-insensitivity syndrome HSDN C0011991 Loose stools C0024198 Lyme disease HSDN C0024902 Mastodynia C0034530 Injury radiation HSDN C0042963 Symptoms vomiting C0025160 Megacolon HSDN C4085862 Bothered by nausea C0015927 Intrauterine fetal demise HSDN C0518090 Frequency of pain question C0035321 Retinal tear HSDN C0853986 Lymphocytes decreased C2936502 Charge syndrome, familial MalaCards C1962972 Proteinuria adverse event C2919796 Glycogen storage disease type ia MalaCards C4084784 Diarrhea C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0426579 Anorexia symptom C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C1963170 Hypothermia adverse event C0014457 Eosinophilia HSDN C0020672 Body temperature decreased C0022638 Ketosis HSDN C0018772 Deafness C0021295 Infant, premature, diseases HSDN C4084784 Diarrhea C0024638 Class ii division 2 malocclusion HSDN C0024032 Birth weight subnormal C0268360 Osteogenesis imperfecta, recessive perinatal lethal HPO C0728710 Pupil constriction observed C2749345 Refsum disease, adult, 1 HPO C0010200 Cough symptom C0867389 Chronic graft-versus-host disease MalaCards C0007398 Catatonic C0010598 Cyclothymic disorder HSDN C0018784 Deafness sensorineural C0027927 Neurosyphilis HSDN C0040822 D tremors C0021670 Insulinoma OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0026850 Muscular dystrophy HSDN C1963281 Vomiting adverse event C1420653 Tcn2 gene HPO C0018772 Deafness C1145628 Autonomic nervous system disorders HSDN C0035232 Diaphragmatic paralysis C1306794 Wound botulism OrphaNet|MalaCards C2242996 Tingling C0011428 Dentigerous cyst HSDN C2984058 Have pain C0027809 Neurilemmoma MalaCards C0085636 Light sensitivity C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C3463815 Feel fatigue C0014121 Bacterial endocarditis HSDN C0024032 Birth weight subnormal C2678312 Three m syndrome 1 HPO C0015938 Fetal macrosomia C1257763 Overnutrition HSDN C3665492 Pigmentations C1832174 Doyne honeycomb retinal dystrophy MalaCards C4084768 Usual severity vomiting C0027625 Circulating neoplastic cells HSDN C1963065 Apnea adverse event C1690964 Cataract HSDN C0242936 Center pain C0751922 Median neuropathy HSDN C0917816 Deficiency mental C0796031 Malouf syndrome HPO C0011991 Loose stools C1546949 Event consequence - death HSDN C4085661 Usual severity nausea C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C4085862 Bothered by nausea C0019243 Angioedemas, hereditary HSDN C4085210 Usual severity pain C0035457 Rhinitis, allergic, perennial HSDN C1963067 Atrial fibrillation adverse event C2678484 Long qt syndrome 10 HPO C0013421 Dystonia C0856066 Dystonia aggravated UMLS C1963063 Anorexia adverse event C0042373 Vascular diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0023283 Leishmaniasis, cutaneous HSDN C0020450 Hyperemesis gravidarum C0860603 Anxiety symptoms HSDN C0013421 Dystonia C1853578 Neuroferritinopathy OrphaNet|HPO|MalaCards C0009421 Comatose C0021400 Influenza HSDN C0454644 Delayed language development C0432255 Geroderma osteodysplastica MalaCards|HPO C0234146 Absent reflex C0795956 Chylomicron retention disease MalaCards|HPO C3815497 Cough C0004364 Autoimmune diseases HSDN C0413252 Hypothermia due to exposure C0007873 Uterine cervical neoplasm HSDN C0013456 Pain ear C0035243 Respiratory tract infections HSDN C0008031 Pain chest C0037286 Skin neoplasms HSDN C0241210 Speaking delay C2936346 22q11 deletion syndrome MalaCards C0027066 Myoclonic jerking C0034885 Rectal neoplasms HSDN C3898969 Have been vomiting C0040411 Tongue neoplasms HSDN C2024878 Cardiovascular surgery result: dyspnea C0279607 Adult primary hepatocellular carcinoma MalaCards C4084776 Weight loss C0004659 Bacteriuria HSDN C0019209 Large liver C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0000737 Abdomen pain C1707406 Clear cell intrahepatic cholangiocarcinoma UMLS C0041657 Consciousness loss C4085311 Depression - recess HSDN C0151889 Reflexes tendon increased C1855008 Mitochondrial complex ii deficiency MalaCards|HPO C3665347 Vision impaired C3280544 Mental retardation, autosomal recessive 25 MalaCards C0037316 Not enough sleeping C0679057 Consolidation memory HSDN C0004093 Asthenia C0023437 Acute basophilic leukemia HSDN C1384666 Decreased hearing C0032343 Poisoning HSDN C0426579 Anorexia symptom C0004943 Behcet syndrome MalaCards|HPO C0234132 Pyramidal sign C0086795 Pfaundler-hurler syndrome HPO C1384666 Decreased hearing C0919267 Ovarian neoplasm HSDN C0009806 Constipate C0029106 Opisthorchiasis DiseaseOntology C0241157 Skin pustule C1858361 Pyogenic arthritis, pyoderma gangrenosum and acne OrphaNet|HPO|MalaCards C0233844 Awkwardness C1866282 Ceroid lipofuscinosis, neuronal, 6 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0701818 Choledocholithiasis HSDN C2126171 Sore on top of mouth C0149745 Oral ulcer UMLS C1963137 Hydrocephalus adverse event C0265863 Dextrocardia, isolated MalaCards C1963087 Constipation adverse event C0017612 Glaucoma, open-angle HSDN C4084766 Vomiting C0011168 Deglutition disorders HSDN C0009806 Constipate C2073625 X-ray of chest: pleural effusion HSDN C1384666 Decreased hearing C2675463 Chromosome 15q26-qter deletion syndrome MalaCards C0013395 Indigestion C0007137 Squamous cell carcinoma HSDN C0242670 Chronic vegetative state C0270726 Alexander disease HSDN C0023380 Lethargy C0016470 Food allergy HSDN C0151798 Liver necrosis C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C0030193 Sense of pain C0334566 Ghost cell odontogenic carcinoma UMLS C1963170 Hypothermia adverse event C0013922 Embolism HSDN C0010520 Skin cyanosis C0024121 Lung neoplasms HSDN C1279888 Proteinuria of undiagnosed cause C0013182 Drug allergy HSDN C0027066 Myoclonic jerking C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards|UMLS C1963071 Back pain adverse event C0026598 Movement perception HSDN C2911645 Weight loss adverse event C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C2237041 Shox gene with short stature C3808414 Perrault syndrome 3 MalaCards C3665347 Vision impaired C2931788 Atypical hemolytic uremic syndrome MalaCards C0000737 Abdomen pain C3272464 Ampulla of vater hepatoid adenocarcinoma UMLS C0009421 Comatose C0025521 Inborn errors of metabolism HSDN C0030193 Sense of pain C0740392 Infarction, middle cerebral artery HSDN C4085317 Diarrhea frequency C0037274 Dermatologic disorders HSDN C4084769 Vomiting frequency C1556682 Adverse event associated with infection HSDN C0557874 Global developmental delay C0242387 Mandibulofacial dysostosis MalaCards|HPO C0151786 Weakness muscle C0162872 Aortic aneurysm, thoracic HSDN C0004941 Behavioral symptoms C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C2237041 Shox gene with short stature C0432291 Mandibuloacral dysostosis MalaCards C3146279 Coma C0038160 Staphylococcal infections HSDN C0030552 Paralysis partial C0004936 Mental disorders HSDN C0018681 Headache, cephalalgia C0027666 Neoplasms, radiation-induced HSDN C0018777 Deafness, conductive C0220742 Bixler christian gorlin syndrome MalaCards C4049644 Depression C0030567 Parkinson disease MalaCards C0009421 Comatose C0006434 Burn injury HSDN C3887638 Failure to thrive in infant C0796095 Opitz trigonocephaly syndrome MalaCards|HPO C0018772 Deafness C0039128 Syphilis HSDN C0002965 Crescendo angina C0041755 Adverse reaction to drug HSDN C0010200 Cough symptom C0043251 Wounds and injuries HSDN C0015970 Fever unknown origin C0007137 Squamous cell carcinoma HSDN C0349588 Stature short C0796123 Cataract-ataxia-deafness-retardation syndrome OrphaNet|MalaCards C0027498 Nausea vomiting C0027873 Neuromyelitis optica MalaCards C0030193 Sense of pain C2350521 Gustatory perception HSDN C0013604 Edematous C0038363 Aphthous stomatitis HSDN C0751495 Seizure focal C0085315 Toxoplasmosis, cerebral UMLS C1963281 Vomiting adverse event C1962979 Burn adverse event HSDN C0030193 Sense of pain C0026618 Dental fluorosis, acquired HSDN C1279888 Proteinuria of undiagnosed cause C0026785 Munchhausen syndrome HSDN C4084897 Sleep disturbance subordinate domain C1835614 Hereditary hyperexplexia MalaCards C0028738 Nystagmus C3150127 Bardet biedl syndrome 15 HPO C0009806 Constipate C0032787 Postoperative complications HSDN C2242996 Tingling C0033578 Prostatic neoplasms HSDN C0023380 Lethargy C0007282 Carotid stenosis HSDN C0231835 Respiration rate increased C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards C0018784 Deafness sensorineural C2750452 Waardenburg syndrome, type 4c MalaCards|HPO C0040264 Ear ringing sound C2717757 Retinocochleocerebral vasculopathies MalaCards C4085211 Pain distress question C0032087 Plant poisoning HSDN C0085642 Asphyxia reticularis C0031117 Peripheral neuropathy HSDN C0542476 Forgetful C0205898 Pineoblastoma OrphaNet|MalaCards C0030193 Sense of pain C0035204 Respiration disorders HSDN C0004134 Dyssynergia C0039373 Tay-sachs disease OrphaNet|MalaCards C0036659 Sensation disorder C0439849 Relationship HSDN C0040034 Thrombocytopenia C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C2237041 Shox gene with short stature C2752015 Glycogen storage disease xiv MalaCards C1145670 Failure respiratory C3809651 Infantile liver failure syndrome 2 MalaCards C1962972 Proteinuria adverse event C0010038 Corneal opacity HSDN C0023380 Lethargy C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|UMLS|HPO|MalaCards C2237041 Shox gene with short stature C1970808 Xeroderma pigmentosum b-cockayne syndrome HPO C0424755 Fever symptoms C0033817 Pseudomonas infections HSDN C2237041 Shox gene with short stature C1850626 Nathalie syndrome OrphaNet|MalaCards C0085602 Polydypsia C0206172 Diabetic foot HSDN C0036572 Convulsion C3494972 Benign occipital epilepsy of childhood - late onset, intractable UMLS C0751837 Gait ataxic C1418654 Plp1 gene HSDN C0413252 Hypothermia due to exposure C0038436 Post-traumatic stress disorder HSDN C0424755 Fever symptoms C0025472 Mesenteric vascular occlusion HSDN C0547030 Sensory perceptual alteration: visual C2189683 Late cva effects: vision disturbances UMLS C3645897 Unable to restrain urination at night and during the day C0042024 Urinary incontinence UMLS C0013604 Edematous C3278138 Fibrochondrogenesis 1 MalaCards C0009421 Comatose C0275148 Poisoning of animal by plant HSDN C4084784 Diarrhea C0024116 Lung diseases, fungal HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0559260 Congenital scoliosis HSDN C0038990 Sweats C0040156 Thyrotoxicosis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0018994 Hemobilia HSDN C0241137 Skin pallor C0027651 Tumor HSDN C4020887 Photodysphoria C1842362 Hermansky-pudlak syndrome 2 MalaCards|HPO C2984057 Have nausea C0013182 Drug allergy HSDN C0151786 Weakness muscle C0032343 Poisoning HSDN C0010038 Corneal opacity disorder C0033788 Pseudo-hurler polydystrophy OrphaNet|MalaCards C0030554 Abnormal sensation C0162671 Melas syndrome MalaCards|HPO C0042798 Vision dim C0035344 Retinopathy of prematurity HSDN C0042571 Vertigo subjective C1268592 Recurrent labyrinthitis syndrome UMLS C0034150 Skin purpura C1556061 Electric injuries HSDN C2315100 Pediatric failure to thrive C0267662 Congenital chloride diarrhea MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0029401 Osteitis deformans HSDN C0020672 Body temperature decreased C0085426 Gram-positive bacterial infections HSDN C0812426 Kidney problem C0748280 Renal cyst chronic UMLS C0018681 Headache, cephalalgia C0280387 Lymphoepithelioma of the nasopharynx, recurrent UMLS C0020455 Hypergammaglobulinemia C0038356 Stomach neoplasms HSDN C0030193 Sense of pain C0694545 Chest pain syndrome UMLS C0041834 Erythematous condition C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0042571 Vertigo subjective C0037369 Smoking HSDN C0036572 Convulsion C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C3827868 Tachycardia by ecg finding C1837014 Atrial fibrillation, familial, 3 MalaCards|HPO C0242936 Center pain C0042847 Vitamin b 12 deficiency HSDN C0033774 Skin pruritus C0175167 Rash acneform HSDN C0242936 Center pain C0158266 Intervertebral disc degeneration HSDN C0034150 Skin purpura C2363755 Acquired protein s deficiency HPO C1963184 Nystagmus adverse event C3809356 Multiple congenital anomalies-hypotonia-seizures syndrome 3 MalaCards C0917816 Deficiency mental C0543533 Hyperlysinemia, type i MalaCards C0036572 Convulsion C0431109 Choroid plexus carcinoma HPO C0012833 Dizzy C0023530 Leukopenia HSDN C0030554 Abnormal sensation C0751911 Paraneoplastic syndromes, nervous system HSDN C4085661 Usual severity nausea C0007099 Carcinoma in situ HSDN C0426579 Anorexia symptom C0024620 Primary malignant neoplasm of liver MalaCards C0271215 Blindness legal C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C0518090 Frequency of pain question C0003708 Arachnitis HSDN C0557874 Global developmental delay C2751195 Epilepsy, benign neonatal, 1, and-or myokymia HPO C3641756 Have diarrhea C0002940 Aneurysm HSDN C0413252 Hypothermia due to exposure C0022665 Kidney neoplasm HSDN C0917816 Deficiency mental C0268151 Classical galactosemia OrphaNet|HPO|MalaCards C0018772 Deafness C0005967 Bone neoplasms HSDN C0018681 Headache, cephalalgia C4029297 Ergotamine induced headache without intractable headache UMLS C4085549 Dizziness C0997768 Glaucoma HSDN C2984057 Have nausea C0020523 Immediate hypersensitivity HSDN C2237041 Shox gene with short stature C0796162 Sonoda syndrome OrphaNet|MalaCards C1963180 Neck pain adverse event C2984289 Melanoma pathway HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0031090 Periodontal diseases HSDN C0042963 Symptoms vomiting C0010074 Coronary vessel anomalies HSDN C0003862 Pain joint C0549143 Pulmonary renal syndrome MalaCards C0000727 Abdomen acute C0039223 Tabes dorsalis HSDN C0023012 Delay language C1414025 Dgcr gene HPO C4085317 Diarrhea frequency C0398791 Nijmegen breakage syndrome MalaCards|HPO C4085549 Dizziness C0037305 Neoplasm, skull HSDN C0263540 Nail loss C1148551 X-linked dyskeratosis congenita MalaCards|UMLS C3665347 Vision impaired C3280392 Edict syndrome MalaCards C0085636 Light sensitivity C0016236 Flicker fusion HSDN C1963091 Diarrhea adverse event C2711227 Steatohepatitis HSDN C0036572 Convulsion C0746536 Mental status altered confusional state acute UMLS C4085222 Nausea C0206715 Neoplasms, neuroepithelial HSDN C0518090 Frequency of pain question C0242172 Pelvic inflammatory disease HSDN C0700078 Deep tendon reflex decrease C1843225 Charcot-marie-tooth disease, axonal, type 2e (disorder) HPO C0035229 Respiratory function impaired C3543825 Ciliary dyskinesia, primary, 18 MalaCards C0518090 Frequency of pain question C1306503 Congenital exomphalos HSDN C4084725 Usual severity cough C0014013 Empyema, pleural DiseaseOntology|HSDN C0270795 Monopareses C0393808 Charcot-marie-tooth disease, x-linked, 1 UMLS C2910386 Tachypnea, not elsewhere classified C0810021 Other lower respiratory disease UMLS C3665492 Pigmentations C0205824 Liposarcoma, dedifferentiated MalaCards C0015672 Decreased energy C0010068 Coronary heart disease HSDN C1963063 Anorexia adverse event C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C1963071 Back pain adverse event C0013394 Coitus painful HSDN C2984058 Have pain C0012752 Distance discrimination HSDN C0036572 Convulsion C1845862 Creatine deficiency, x-linked OrphaNet|UMLS|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0001849 Aids dementia complex HSDN C2911647 Weight gain adverse event C0019163 Hepatitis b HSDN C0042420 Vasovagal episode C1579931 Depressed - symptom HSDN C0033774 Skin pruritus C1288283 Atrophoderma maculatum HSDN C0040264 Ear ringing sound C0018802 Congestive heart failure HSDN C0011206 Delirium acute C0007222 Cardiovascular diseases HSDN C3641756 Have diarrhea C0042164 Uveitis HSDN C0042963 Symptoms vomiting C3273126 Extrahepatic bile duct adenocarcinoma, biliary type UMLS C0013428 Painful urination C1384606 Dyspareunia HSDN C0042963 Symptoms vomiting C0042830 Perception visual HSDN C0031911 Pigment deposition C0153463 Malig neop oth spec pancreas MalaCards C1510456 Wernicke aphasia C0014547 Epilepsies, partial HSDN C0013362 Dysarthrias C1443901 Intestinal botulism OrphaNet|MalaCards C0040485 Wryneck C0270969 Zebra body myopathy OrphaNet|HPO|MalaCards C3146279 Coma C0020701 Somatization disorder HSDN C0575081 Abnormal gait C1300260 Spondylar and nasal alterations with striated metaphyses OrphaNet|MalaCards C0013456 Pain ear C0027858 Neuroma HSDN C0812426 Kidney problem C0020545 Hypertension, renovascular UMLS C0243026 Generalized infection C1864996 Enteric neuropathy, familial MalaCards C0518090 Frequency of pain question C0393571 Multiple system atrophy HSDN C0030193 Sense of pain C0023348 Leprosy, lepromatous HSDN C0349506 Sun sensitivity C2752147 Xeroderma pigmentosum, complementation group c HPO C0040034 Thrombocytopenia C3809031 Neutropenia, severe congenital, 5, autosomal recessive MalaCards C0039070 Collapse fleeting C0018817 Atrial septal defects HSDN C0424755 Fever symptoms C0015726 Focused anxiety HSDN C0242936 Center pain C0014854 Esophageal diverticulum HSDN C2096293 Ent surgical result ear vertigo C0036341 Schizophrenia HSDN C4084784 Diarrhea C0162534 Prion diseases HSDN C0004604 Pain back C0233629 Thinking and speaking disturbances HSDN C0151786 Weakness muscle C0268060 Juvenile hemochromatosis OrphaNet|HPO|MalaCards C3665347 Vision impaired C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO C0040822 D tremors C0041374 Tumor virus infections HSDN C2919142 Short stature adverse event C0795939 Aminopterin syndrome sine aminopterin MalaCards C0015672 Decreased energy C0030499 Parasitic diseases HSDN C0042963 Symptoms vomiting C0011615 Dermatitis, atopic HSDN C0030193 Sense of pain C1708650 Laryngeal basaloid carcinoma UMLS C2919142 Short stature adverse event C1853576 Diamond-blackfan anemia with microtia and cleft palate HPO C4085862 Bothered by nausea C0270611 Brain damage HSDN C0242936 Center pain C0016059 Fibrosis HSDN C1963281 Vomiting adverse event C0020701 Somatization disorder HSDN C0751837 Gait ataxic C1861301 Syringomyelia, isolated UMLS C0022346 Yellow skin C0015802 Femur fracture HSDN C0497247 Blood pressure elevation C1867774 Sacral agenesis syndrome HPO C0015672 Decreased energy C2945560 Hemolytic HSDN C0042940 Disorder of voice C0242387 Mandibulofacial dysostosis HSDN C1549543 Administration method - pain C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C0242936 Center pain C0006264 Bronchial neoplasms HSDN C0557874 Global developmental delay C1836706 Hyperthyroidism, nonautoimmune MalaCards C0028738 Nystagmus C1848533 Ataxia with vitamin e deficiency OrphaNet|HPO C1963063 Anorexia adverse event C0235974 Pancreatic carcinoma MalaCards C0018681 Headache, cephalalgia C0018621 Hay fever HSDN C0497406 Over weight C0023470 Myeloid leukemia HSDN C4084725 Usual severity cough C0003504 Aortic valve insufficiency HSDN C0237326 Defecation pain C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C1069915 Vertigo C0270639 Lateral sinus thrombosis HSDN C4085211 Pain distress question C0242172 Pelvic inflammatory disease HSDN C1963086 Confusion adverse event C0268543 Hyperammonemia, type iii MalaCards|HPO C2029884 Hearing loss by exam C0259779 Fibrous dysplasia HSDN C0036572 Convulsion C3890168 Mental retardation, x-linked 101 MalaCards C0026838 Spasticity muscle C0030286 Pancreatic diseases HSDN C0036572 Convulsion C0023473 Myeloid leukemia, chronic HSDN C4084766 Vomiting C0030330 Panniculitis, peritoneal HSDN C0013604 Edematous C0031024 Suppurative periapical periodontitis HSDN C0026838 Spasticity muscle C2936859 N syndrome OrphaNet|MalaCards C4084726 Distress cough C2930674 Babesioses, human MalaCards C1860844 Sparse, thin hair C3554448 Mental retardation, autosomal dominant 18 MalaCards C1963281 Vomiting adverse event C0027947 Neutropenia HSDN C0024032 Birth weight subnormal C1848862 Miller-mckusick-malvaux-syndrome (3m syndrome) HPO C4042891 Sleep wake disorders C0677838 Grief loss HSDN C0009806 Constipate C0221043 Liddle syndrome OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0015397 Disorder of eye HSDN C0015300 Ocular proptosis C0041409 Turner syndrome, male MalaCards C4085317 Diarrhea frequency C0043254 Injuries penetrating HSDN C0270846 Astatic seizure C1848137 Epilepsy, female-restricted, with mental retardation (disorder) MalaCards|HPO C0030554 Abnormal sensation C0030472 Paraneoplastic syndromes HSDN C0018777 Deafness, conductive C0038987 Sweat gland neoplasms HSDN C0151786 Weakness muscle C0398791 Nijmegen breakage syndrome MalaCards|HPO C0015469 Facial paralysis C0020437 Hypercalcemia HSDN C3898969 Have been vomiting C0004610 Bacteremia HSDN C0036572 Convulsion C0043241 Wound infection HSDN C4084769 Vomiting frequency C0011168 Deglutition disorders HSDN C3829611 Nausea frequency C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C0344428 Ventricular tachycardia by ecg finding C3810138 Arrhythmogenic right ventricular dysplasia, familial, 13 MalaCards C3665346 Loss sight C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0003469 Anxiety disorder C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C0007758 Cerebellar ataxia C3539916 Myoclonus, familial cortical MalaCards C4084724 Usual severity constipation C1394494 Cystocele, unspecified HSDN C4084776 Weight loss C0002989 Epithelioid hemangioma of skin HSDN C0030552 Paralysis partial C0036202 Sarcoidosis HSDN C0024031 Back pain lower back C0029463 Osteosarcoma HSDN C0008031 Pain chest C0795623 Hepatitis a vaccine, inactivated HSDN C0030554 Abnormal sensation C0003851 Arteriosclerosis obliterans HSDN C0151686 Growth retardation C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0030486 Extremity paralysis, lower C0021799 Interprofessional relations HSDN C0004134 Dyssynergia C1837355 Leukodystrophy, hypomyelinating, 2 MalaCards|HPO|UMLS C0020305 Fetal edema C1857663 Yunis varon syndrome MalaCards|HPO C4084776 Weight loss C0027726 Nephrotic syndrome HSDN C0036572 Convulsion C0002992 Angiomatosis HSDN C2024893 Cardiovascular surgery result: fatigue C0030793 Pelvis tumor HSDN C0011206 Delirium acute C0001940 Alcohol amnestic disorder HSDN C4085661 Usual severity nausea C0011615 Dermatitis, atopic HSDN C0035232 Diaphragmatic paralysis C0001126 Renal tubular acidosis HSDN C0010520 Skin cyanosis C0019163 Hepatitis b HSDN C0242936 Center pain C0002986 Fabry disease HSDN C0019521 Hiccoughs C0019284 Diaphragmatic hernia HSDN C0011991 Loose stools C0029422 Osteochondrodysplasias HSDN C4084776 Weight loss C2347126 Microscopic polyarteritis HSDN C0241210 Speaking delay C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C3815497 Cough C0010709 Cyst HSDN C0917816 Deficiency mental C1855126 3-methylglutaconic aciduria type iv OrphaNet|MalaCards C1549543 Administration method - pain C0008370 Cholestasis HSDN C0018772 Deafness C0265246 Townes syndrome OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0030283 Pancreatic cyst HSDN C0494475 Seizure generalized tonic clonic C1969054 Glycogen storage disease 0, muscle MalaCards|HPO C0424755 Fever symptoms C0003490 Aortic arch syndrome MalaCards|HSDN C0013604 Edematous C0041234 Chagas disease OrphaNet|HSDN|MalaCards C0237326 Defecation pain C0037661 Somatostatinoma OrphaNet|MalaCards C0018681 Headache, cephalalgia C3542413 Cdisc adas-cog - comprehension HSDN C0036572 Convulsion C1847501 Glut1 deficiency syndrome OrphaNet|MalaCards C0018681 Headache, cephalalgia C0001175 Acquired immunodeficiency syndrome HSDN|UMLS C4085210 Usual severity pain C0005747 Blepharospasm HSDN C0013421 Dystonia C1857252 2,4-dienoyl-coa reductase deficiency MalaCards C0009676 Confusion state C0085541 Epilepsy, frontal lobe HSDN C1069915 Vertigo C1832475 Deafness, autosomal dominant 11 MalaCards|HPO C0522224 Palsied C0033975 Psychotic disorders HSDN C1963091 Diarrhea adverse event C0008384 Cholesterol ester storage disease OrphaNet|HPO C2029884 Hearing loss by exam C0265240 Goldenhar syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026918 Mycobacterium infections HSDN C0031911 Pigment deposition C0155169 Conjunctival hyperemia MalaCards C0033377 Caudal displacement C1864233 Endplate acetylcholinesterase deficiency (disorder) MalaCards|HPO C2029884 Hearing loss by exam C2698658 Orofaciodigital syndrome type 1 MalaCards C4084723 Constipation C0006118 Brain neoplasms HSDN C1069915 Vertigo C0007134 Renal cell carcinoma HSDN C1963091 Diarrhea adverse event C0027540 Necrosis HSDN C0009806 Constipate C1856113 Mowat-wilson syndrome MalaCards|HPO|UMLS C0012569 Double vision C0220847 C hepatitis virus HSDN C2203646 Jaundice C0850803 Anaphylaxis (non medication) HSDN C0518090 Frequency of pain question C0002940 Aneurysm HSDN C0917816 Deficiency mental C3696898 Autosomal dominant nocturnal frontal lobe epilepsy MalaCards C4084802 Usual severity diarrhea C0015652 Fascioliasis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038016 Spondylolisthesis HSDN C0037316 Not enough sleeping C0007682 Cns disorder HSDN C4084769 Vomiting frequency C0006840 Candidiasis HSDN C3898969 Have been vomiting C0031485 Phenylketonurias HSDN C0001707 Aerophagia C0034067 Pulmonary emphysema HSDN C4049602 Hyperactivity C0041671 Attention deficit disorder MalaCards C3274924 Have been coughing C0011334 Dental caries HSDN C0917816 Deficiency mental C0265962 Ichthyosis linearis circumflexa OrphaNet|HPO|MalaCards C0267373 Bleeding intestine C1333088 Colonic hamartomatous polyps MalaCards C0030193 Sense of pain C0006666 Calciphylaxes HSDN C0042798 Vision dim C0751544 Tangier disease neuropathy MalaCards C3887638 Failure to thrive in infant C2749477 Oculodentodigital dysplasia, autosomal recessive MalaCards|HPO C0020796 Profoundly mentally retarded C0342770 Fumarase deficiency MalaCards|HPO C0039070 Collapse fleeting C0262655 Recurrent urinary tract infection HSDN C0018784 Deafness sensorineural C1858028 Wolfram syndrome 2 MalaCards|HPO C0848203 Male pelvic pain C0009375 Colonic neoplasms HSDN C0600142 Flash hot C0027651 Tumor HSDN C1279888 Proteinuria of undiagnosed cause C0031099 Periodontitis HSDN C0231218 Malaise generalized C1332246 Ampulla of vater clear cell adenocarcinoma UMLS C0700078 Deep tendon reflex decrease C2749345 Refsum disease, adult, 1 HPO C3539893 Pelvic pain occurs with intercourse C1550672 Specimen type - ulcer HSDN C0413252 Hypothermia due to exposure C0008626 Congenital chromosomal disease HSDN C0085631 Abnormal excitement C0268560 Hyperglycinemia, transient neonatal HPO C0085631 Abnormal excitement C0021368 Inflammation HSDN C0000731 Abdomen distention C0948039 Bacterial gastritis MalaCards C0424755 Fever symptoms C0559260 Congenital scoliosis HSDN C4084784 Diarrhea C0206718 Ganglioneuroblastoma HSDN C0030554 Abnormal sensation C1834304 Amyotrophy, hereditary neuralgic MalaCards C0042963 Symptoms vomiting C0023267 Fibroid tumor HSDN C1838869 Proximal neurogenic muscle weakness C1836050 Filaminopathy, autosomal dominant MalaCards|HPO C0019209 Large liver C1856476 Gaucher disease, type iiic MalaCards|HPO C0026858 Musculoskeletal pain C0001828 Agricultural workers' diseases HSDN C0853986 Lymphocytes decreased C0685894 Congenital absence of thymus MalaCards C0018777 Deafness, conductive C0026363 Mohr-claussen syndrome MalaCards C0221752 Rbc urine C0220989 Acquired partial lipodystrophy MalaCards C0010200 Cough symptom C0398370 Lipedema HSDN C0027498 Nausea vomiting C0206719 Central neurocytoma OrphaNet|MalaCards C3641756 Have diarrhea C0016952 Galactosemias MalaCards C0040460 Dental pain C1962986 Glaucoma adverse event HSDN C2029884 Hearing loss by exam C3814778 Hemolytic index HSDN C0742354 Chest wall pain musculoskeletal C0029408 Degenerative polyarthritis UMLS C0746674 Muscle weakness generalized C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO|UMLS C1963077 Bone pain adverse event C1960539 Aromatase deficiency OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0023220 Leg injury HSDN C1557397 Adverse event associated with pain C1852551 Epithelial recurrent erosion dystrophy MalaCards|HPO C0085636 Light sensitivity C0456892 Csf low pressure HSDN C4084773 Bothered by weight gain C0029408 Degenerative polyarthritis HSDN C2984058 Have pain C0012691 Dislocations HSDN C0032285 Pneum C1865370 Severe combined immunodeficiency with sensitivity to ionizing radiation HPO C3641756 Have diarrhea C0021364 Male infertility HSDN C1963252 Tremor adverse event C2931004 Congenital disorder of glycosylation type 1j MalaCards C4084769 Vomiting frequency C0002949 Aneurysm, dissecting HSDN C3641755 Have constipation C1548484 Rheumatic fever vaccine HSDN C0151786 Weakness muscle C2711227 Steatohepatitis HSDN C4084788 Have dizziness C2827407 Infectious otitis media HSDN C4084769 Vomiting frequency C4049994 Insulin resistance measurement HSDN C1557397 Adverse event associated with pain C0005689 Bladder exstrophy HSDN C4084774 Have weight loss C0016658 Fracture bone HSDN C0027066 Myoclonic jerking C0428953 Ecg infarction myocardial HSDN C0018772 Deafness C0220681 Goldenhar syndrome with ipsilateral radial defect MalaCards C2919142 Short stature adverse event C2936502 Charge syndrome, familial MalaCards C0008031 Pain chest C0003504 Aortic valve insufficiency HSDN C0013604 Edematous C0017185 Gastrointestinal neoplasms HSDN C0018681 Headache, cephalalgia C1546747 Specimen source codes - polyps HSDN C0812426 Kidney problem C0746837 Nephropathy incipient UMLS C3815497 Cough C1546533 Specimen source codes - abscess HSDN C0035078 Failure kidney C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C0233514 Behavior abnormal C0087012 Ataxia, spinocerebellar MalaCards C0221752 Rbc urine C0867389 Chronic graft-versus-host disease MalaCards C1557397 Adverse event associated with pain C0162830 Dermatitis, phototoxic HSDN C0022346 Yellow skin C0012817 Diverticulum HSDN C4084767 Bothered by vomiting C0268621 Hepatic methionine adenosyltransferase deficiency MalaCards C0231791 In toe C1855305 Ter haar syndrome MalaCards|HPO C0016204 Fart C1720887 Female urogenital diseases HSDN C0746674 Muscle weakness generalized C1969443 Trifunctional protein deficiency with myopathy and neuropathy HPO C4084767 Bothered by vomiting C0031485 Phenylketonurias HSDN C0026821 Cramp C0015458 Facial hemiatrophy HSDN C0020580 Decreased sensation C0029456 Osteoporosis HSDN C0038002 Spleen enlargement C1842704 Gaucher disease, perinatal lethal OrphaNet|HPO|MalaCards C0042940 Disorder of voice C0040128 Thyroid diseases HSDN C1963137 Hydrocephalus adverse event C1838257 Serpentine fibula polycystic kidney syndrome MalaCards C0019079 Bloody sputum C0020542 Pulmonary hypertension UMLS C0018772 Deafness C0003811 Cardiac arrhythmia HSDN C0497406 Over weight C0026650 Movement disorders HSDN C4084774 Have weight loss C0345904 Malignant neoplasm of liver MalaCards C0042384 Vasculitis, nonspecific C3812646 Drug induced cutaneous vasculitis MalaCards C0004604 Pain back C0702221 Tactual discrimination HSDN C0034933 Abnormal reflexes C0010054 Coronary arteriosclerosis HSDN C0026821 Cramp C0038981 Swayback HSDN C0151908 Dry skin C0151467 Addisonian crisis MalaCards C4084725 Usual severity cough C0872315 Communicable diseases emerging HSDN C0237849 Skin desquamation C1849193 Peeling skin syndrome MalaCards|HPO C4085211 Pain distress question C0022593 Keratosis HSDN C0242936 Center pain C0037199 Sinusitis HSDN C0019079 Bloody sputum C1336184 Stage iib large cell carcinoma of lung UMLS C0085631 Abnormal excitement C0018674 Head trauma HSDN C1565249 Limitation, mobility C0079631 Interdisciplinary communication HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0460137 Push down or depress HSDN C3641756 Have diarrhea C0009326 Collagen diseases HSDN C0042798 Vision dim C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO C0013604 Edematous C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome OrphaNet|MalaCards C0042571 Vertigo subjective C0040128 Thyroid diseases HSDN C0700078 Deep tendon reflex decrease C4014648 Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 MalaCards C0030554 Abnormal sensation C0042338 Herpesvirus 3, human HSDN C0221263 Cafe au lait spot C1838457 Fanconi anemia, complementation group d1 HPO C1557397 Adverse event associated with pain C0019562 Von hippel-lindau syndrome HSDN C2984058 Have pain C0019556 Canine hip dysplasia HSDN C0004134 Dyssynergia C0019187 Hepatitis, alcoholic UMLS C4084766 Vomiting C0497327 Dementia HSDN C2242996 Tingling C0340957 Congenital deficiency of intrinsic factor MalaCards C0026205 Pupillary constriction C0038663 Suicide attempt HSDN C0027066 Myoclonic jerking C1876175 Ataxia-telangiectasia variant MalaCards|HPO C2203646 Jaundice C0153458 Pancreas head cancer malignant MalaCards C1963170 Hypothermia adverse event C0040046 Thrombophlebitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013592 Ectropion HSDN C0743973 Fever high C0019100 Severe dengue DiseaseOntology|MalaCards C0011991 Loose stools C0278061 Abnormal mental state UMLS C1963252 Tremor adverse event C0026552 Morphine dependence HSDN C0042571 Vertigo subjective C0022876 Premature obstetric labor HSDN C0011991 Loose stools C0018021 Goiter HSDN C1549543 Administration method - pain C0152025 Polyneuropathy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019285 Diaphragmatic hernia traumatic HSDN C0751837 Gait ataxic C1552527 Clinic / center - developmental disabilities HSDN C0030193 Sense of pain C0151526 Premature birth HSDN C0042963 Symptoms vomiting C3665493 Snake bites HSDN C0043094 Weight gain C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C4084774 Have weight loss C0013182 Drug allergy HSDN C0851578 Disorder sleep C1623041 Breast-fed HSDN C2880347 Corneal deposits in metabolic disorders, unspecified eye C0497217 Other disease of eye UMLS C0009421 Comatose C0018916 Hemangioma HSDN C0043094 Weight gain C0027947 Neutropenia HSDN C2911645 Weight loss adverse event C0153458 Pancreas head cancer malignant MalaCards C4084774 Have weight loss C0042140 Uterine prolapse HSDN C1549543 Administration method - pain C0085110 Severe combined immunodeficiency HSDN C0398650 Idiopathic thrombocytopenia purpura C0162359 Christ-siemens-touraine syndrome HSDN C0030193 Sense of pain C0280352 Adenoid cystic carcinoma of the oral cavity, stage ii UMLS C0030193 Sense of pain C0264676 Angina, class ii UMLS C0037316 Not enough sleeping C1263846 Attention deficit hyperactivity disorder HSDN C0003862 Pain joint C0477611 Spin osteochondrosis, unsp HSDN C0018965 Blood urine C0281479 Primary systemic amyloidosis MalaCards C0085642 Asphyxia reticularis C0030578 Paronychia inflammation HSDN C0009398 Color vision defects C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4085222 Nausea C1253943 Fluid in the chest HSDN C4085210 Usual severity pain C0221757 Alpha 1-antitrypsin deficiency HSDN C1549543 Administration method - pain C0019061 Hemolytic-uremic syndrome HSDN C3829611 Nausea frequency C0017658 Glomerulonephritis HSDN C0016382 Cutaneous vascular engorgement C0017531 Angiolymphoid hyperplasia HSDN C3665347 Vision impaired C1852759 Papillorenal syndrome OrphaNet|HPO|MalaCards C0917816 Deficiency mental C1837429 Pyruvate dehydrogenase phosphatase deficiency MalaCards|HPO C3898969 Have been vomiting C0032229 Pleural neoplasms HSDN C0020649 Blood pressure decreased C0151467 Addisonian crisis OrphaNet|MalaCards C0013421 Dystonia C0342286 Woodhouse sakati syndrome OrphaNet|HPO|MalaCards C0013395 Indigestion C0812393 Cancer patients and suicide and depression HSDN C0010200 Cough symptom C1336173 Stage iia squamous cell carcinoma of lung UMLS C4084775 Usual severity weight loss C0003857 Congenital arteriovenous malformation HSDN C1963281 Vomiting adverse event C0025222 Melena HSDN C4085210 Usual severity pain C0175702 Williams syndrome HSDN C0030552 Paralysis partial C1420653 Tcn2 gene HPO C4085317 Diarrhea frequency C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C0030193 Sense of pain C0393735 Headache disorders HSDN|UMLS C0037763 Spasm C0038160 Staphylococcal infections HSDN C4084767 Bothered by vomiting C0036231 Sarcocystosis DiseaseOntology C3815497 Cough C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0013404 Respiratory difficulty C0342257 Complications of diabetes mellitus HSDN C2012601 Lymph node swelling in right groin C0578736 Inguinal lymphadenopathy UMLS C0042025 Urinary incontinence stress C0001721 Emotional affect HSDN C2919142 Short stature adverse event C0795917 Alpha-thalassemia mental retardation syndrome, deletion-type OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0020546 Hypertensive crisis UMLS C1963170 Hypothermia adverse event C0014761 Erythroblastosis, fetal HSDN C0034150 Skin purpura C0023895 Liver diseases HSDN C0027497 Queasy C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0013362 Dysarthrias C4014812 Spinocerebellar ataxia 38 MalaCards C3815497 Cough C0019114 Hemosiderosis HSDN C0000737 Abdomen pain C1336309 Ovarian polyembryoma stage ii UMLS C0004134 Dyssynergia C0005745 Blepharoptosis HSDN C1963063 Anorexia adverse event C0002871 Anemia HSDN C1549543 Administration method - pain C0162637 Strongylida infections HSDN C2911645 Weight loss adverse event C0041318 Tuberculosis, meningeal HSDN C0424755 Fever symptoms C0007193 Cardiomyopathy, dilated HSDN C4084768 Usual severity vomiting C0030354 Papilloma HSDN C0454644 Delayed language development C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C0018681 Headache, cephalalgia C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C0027497 Queasy C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C0037763 Spasm C0007682 Cns disorder HSDN C0042571 Vertigo subjective C0242342 Sheehan syndrome MalaCards C4084762 Usual severity shortness of breath C0006277 Bronchitis DiseaseOntology|MalaCards C0043094 Weight gain C0035369 Retroviridae infections HSDN C0042798 Vision dim C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C3274924 Have been coughing C0033348 Language program HSDN C4085210 Usual severity pain C0752143 Intracranial thrombosis HSDN C0009421 Comatose C0024232 Lymphatic metastasis HSDN C0018524 Hallucinate C0003493 Aortic diseases HSDN C3898969 Have been vomiting C0022107 Irritable mood HSDN C0000737 Abdomen pain C1336339 Stage iva hepatocellular carcinoma UMLS C4085210 Usual severity pain C0022575 Keratoconjunctivitis sicca HSDN C0007859 Pain neck C1956346 Coronary artery disease HSDN C0242936 Center pain C0014335 Enteritis HSDN C0010520 Skin cyanosis C2984299 Asthma pathway HSDN C1963184 Nystagmus adverse event C0795914 Crome syndrome OrphaNet|MalaCards C4085222 Nausea C0032851 Disease poultry HSDN C0022346 Yellow skin C2981633 Stage i hilar cholangiocarcinoma UMLS C0020796 Profoundly mentally retarded C1868678 Thanatophoric dysplasia, type i (disorder) OrphaNet|HPO|MalaCards C0010200 Cough symptom C1306577 Dies patient HSDN C4084784 Diarrhea C3814530 Skin vesicle HSDN C4085317 Diarrhea frequency C1261470 Congenital meningocele HSDN C4084723 Constipation C1552962 Units of measure - pica HSDN C0460137 Push down or depress C0001622 Adrenal gland hyperfunction OrphaNet C4084788 Have dizziness C1706377 Memory device component HSDN C4084788 Have dizziness C0005695 Bladder neoplasm HSDN C0030232 Color loss C0004377 Automatism HSDN C0426359 Urinary sign C0152245 Leakage urine UMLS C0026821 Cramp C0410207 Tubular aggregate myopathy MalaCards|HPO C0028738 Nystagmus C0028326 Noonan syndrome MalaCards|HPO C2029884 Hearing loss by exam C0018213 Graves disease HSDN C0242936 Center pain C0302280 Adrenogenital syndrome HSDN C0038002 Spleen enlargement C1720779 Apolipoprotein c-ii deficiency (disorder) HPO C0349588 Stature short C2675860 Diamond-blackfan anemia 4 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0001622 Adrenal gland hyperfunction HSDN C1999266 Depression adverse event C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant HPO C0015230 Exanthem C0221026 X-linked agammaglobulinemia OrphaNet|HPO C2024878 Cardiovascular surgery result: dyspnea C0034084 Pulmonary infundib.stenosis HSDN C0455988 Hydrops fetalis non immune C0268059 Neonatal hemochromatosis MalaCards C0003467 Angst C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C0333410 Deep granuloma annulare C3854000 Granulomatous lesion UMLS C0008031 Pain chest C0037579 Soft tissue neoplasms HSDN C0018681 Headache, cephalalgia C0032788 Postoperative hemorrhage HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0025345 Menstruation disturbances HSDN C0030193 Sense of pain C1511315 Breast inflammatory myofibroblastic tumor UMLS C0015469 Facial paralysis C2931244 Craniometaphyseal dysplasia, autosomal recessive type MalaCards C0040264 Ear ringing sound C0439840 Reflex motion descriptor HSDN C3539896 Pelvic pain occurs with urination C0563150 Catastrophization HSDN C2029884 Hearing loss by exam C0024748 Alpha-mannosidosis HSDN C0036572 Convulsion C1850186 Osteodysplasia, familial, anderson type MalaCards C0018965 Blood urine C1856143 Hemolytic uremic syndrome, typical MalaCards C4084726 Distress cough C0403447 Chronic kidney insufficiency HSDN C0023530 Leukopenia C0268647 Lysinuric protein intolerance MalaCards|HPO C0022346 Yellow skin C0017636 Glioblastoma HSDN C1549543 Administration method - pain C0020545 Hypertension, renovascular HSDN C0349588 Stature short C3150971 Leopard syndrome 3 MalaCards|HPO C0018772 Deafness C0085183 Neoplasms, second primary HSDN C0042928 Paralysis vocal cord C0013743 Eisenmenger complex HSDN C3539890 Pelvic pain causes awakening at night C0005586 Bipolar disorder HSDN C0751837 Gait ataxic C0456892 Csf low pressure HSDN C0042964 Anticipatory vomiting C0007137 Squamous cell carcinoma HSDN C0012569 Double vision C0032965 Pregnancy complications, infectious HSDN C0030486 Extremity paralysis, lower C0013010 Cerebral lateralization HSDN C0042571 Vertigo subjective C0002874 Aplastic anemia HSDN C0264272 Nose discharge, purulent C1290072 Infectious disease of mucous membrane UMLS C3887873 Hearing loss C0025202 Melanoma HSDN C0020672 Body temperature decreased C0007570 Celiac disease HSDN C0000737 Abdomen pain C0009241 Cognition disorders HSDN C3539890 Pelvic pain causes awakening at night C1548578 Location characteristic id - smoking HSDN C0030193 Sense of pain C0279738 Acinic cell tumor, salivary gland UMLS C0040822 D tremors C0265498 48, xxxy syndrome MalaCards C4084726 Distress cough C1720777 Functional laterality HSDN C1090821 Sepsis C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C0038002 Spleen enlargement C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C3815497 Cough C0860603 Anxiety symptoms HSDN C0036572 Convulsion C0027412 Opioid-related disorders HSDN C0030554 Abnormal sensation C0162565 Acute intermittent porphyria OrphaNet|HSDN|HPO|MalaCards C0018777 Deafness, conductive C1833691 Otofaciocervical syndrome OrphaNet|HPO C4084776 Weight loss C0022408 Arthropathy HSDN C1963093 Dizziness adverse event C1556682 Adverse event associated with infection HSDN C1384666 Decreased hearing C1290398 Cerebral arterial aneurysm HSDN C4084776 Weight loss C0023798 Lipoma HSDN C0015300 Ocular proptosis C4014294 Desbuquois dysplasia 2 MalaCards C0007758 Cerebellar ataxia C2676771 Joubert syndrome 8 (disorder) MalaCards C1963281 Vomiting adverse event C1536500 Deficiency of acetyl-coa acetyltransferase MalaCards|HPO C0027497 Queasy C1332552 Bile duct mucoepidermoid carcinoma UMLS C4085211 Pain distress question C1522137 Hypertriglyceridemia result HSDN C0424755 Fever symptoms C2981150 Uranostaphyloschisis HSDN C0518090 Frequency of pain question C1565489 Renal insufficiency HSDN C2132198 Abnormal blistering of the skin C1136033 Cutaneous mastocytosis MalaCards C0019825 Voice hoarseness C0018944 Hematoma HSDN C0024032 Birth weight subnormal C0032051 Placental insufficiency OrphaNet|MalaCards C0042514 Ventricular tachycardia C1969081 Arrhythmogenic right ventricular dysplasia, familial, 12 HPO C1963281 Vomiting adverse event C0007786 Brain ischemia HSDN C3539022 Pelvic pain decreasing in severity C0037929 Spinal cord injuries HSDN C3463815 Feel fatigue C3244301 Coverage level - family HSDN C4084727 Cough frequency C0018273 Growth disorders HSDN C2911645 Weight loss adverse event C0015328 Behavior, exploratory HSDN C1963077 Bone pain adverse event C0029396 Heterotopic ossification MalaCards C4084727 Cough frequency C0032131 Plasmacytoma HSDN C0003862 Pain joint C0003850 Arteriosclerosis HSDN C0242936 Center pain C0027849 Neuroleptic malignant syndrome HSDN C0424755 Fever symptoms C0006107 Concussion HSDN C4085210 Usual severity pain C0035335 Retinoblastoma HSDN C2911645 Weight loss adverse event C0878675 Erdheim-chester disease OrphaNet|HSDN|MalaCards C0022346 Yellow skin C1332253 Ampulla of vater tubulovillous adenoma UMLS C1961131 Cough adverse event C0038940 Surgical wound dehiscence HSDN C0241157 Skin pustule C0406556 Hereditary acrokeratotic poikiloderma of weary OrphaNet|HPO|MalaCards C0242936 Center pain C1963139 Hypopigmentation adverse event HSDN C0333422 Gumma C0276015 Gummatous periostitis of yaws UMLS C0577294 Perianal mass C3266099 Haematoma of perianal region UMLS C0015970 Fever unknown origin C0004030 Aspergillosis HSDN C0036572 Convulsion C1855772 Absent corpus callosum cataract immunodeficiency OrphaNet|UMLS|HPO|MalaCards C4084773 Bothered by weight gain C0026269 Mitral valve stenosis HSDN C0037383 Sneeze C3810814 Myocardial infarction ecg assessment HSDN C0012833 Dizzy C0796561 Melanoma vaccines HSDN C4085210 Usual severity pain C0014072 Experimental autoimmune encephalomyelitis HSDN C0037316 Not enough sleeping C0019159 Hepatitis a HSDN C0344315 Mood depressed C2930798 Alexanders leukodystrophy MalaCards C0004134 Dyssynergia C3150667 Microcephaly, seizures, and developmental delay MalaCards|HPO C0740389 Elbow swelling C3665488 Familial osteochondritis dissecans UMLS C3463815 Feel fatigue C0004442 Avoidance learning HSDN C1000483 Genus anemia C2931087 Achondroplasia and swiss type agammaglobulinemia MalaCards C0023530 Leukopenia C0398794 Hypopigmentation-immunodeficiency disease MalaCards C4085548 Usual severity dizziness C0026771 Trauma multiple HSDN C0018681 Headache, cephalalgia C0393750 External compression headache UMLS C1963091 Diarrhea adverse event C0268416 Enterokinase deficiency MalaCards|HPO C4084724 Usual severity constipation C0030793 Pelvis tumor HSDN C0857305 Thrombocytopenia purpura C2239176 Liver carcinoma HSDN C1963091 Diarrhea adverse event C0241910 Hepatitis, autoimmune HSDN C0042798 Vision dim C3539923 Cdisc adas-cog - orientation summary score HSDN C0012833 Dizzy C0022650 Kidney calculi HSDN C3641756 Have diarrhea C0029106 Opisthorchiasis DiseaseOntology C0518090 Frequency of pain question C0024440 Macular edema, cystoid HSDN C0030193 Sense of pain C0020295 Hydronephrosis HSDN C0019825 Voice hoarseness C1336232 Stage iiib small cell cancer of lung without pleural effusion UMLS C0040034 Thrombocytopenia C0342337 Insulin resistance syndrome, type b MalaCards C0851578 Disorder sleep C0034929 Reflex HSDN C0037383 Sneeze C0043540 Zygomatic fracture HSDN C0023014 Developmental disorder language C0080178 Spina bifida HSDN C1962972 Proteinuria adverse event C0268237 Cytochrome-c oxidase deficiency MalaCards|HPO C2032395 Pelvic pain on the left C0206767 Neoplasms, cystic, mucinous, and serous HSDN C0015672 Decreased energy C0018799 Heart diseases HSDN C0241137 Skin pallor C0023290 Leishmaniasis, visceral HSDN C0019572 Hairiness C0007097 Carcinomas HSDN C1279888 Proteinuria of undiagnosed cause C0039006 Swine--diseases HSDN C0700078 Deep tendon reflex decrease C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C0013595 Eczematous dermatitis C1303073 Nicolaides baraitser syndrome MalaCards|HPO C0860603 Anxiety symptom C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4042891 Sleep wake disorders C0019699 Hiv seropositivity HSDN C1963063 Anorexia adverse event C0022661 Kidney failure, chronic HSDN C4084723 Constipation C0162531 Hereditary coproporphyria OrphaNet|HPO C4084775 Usual severity weight loss C3495422 Finding relating to sexuality and sexual activity HSDN C0557874 Global developmental delay C0271972 Thiamine-responsive megaloblastic anemia MalaCards C0398650 Idiopathic thrombocytopenia purpura C0029456 Osteoporosis HSDN C0752303 Manifestation, urological C0262655 Recurrent urinary tract infection HSDN C0015672 Decreased energy C0041296 Tuberculosis OrphaNet|HPO|UMLS C0155552 Hearing loss mixed C0021355 Infective otitis externa HSDN C0575081 Abnormal gait C0917713 Becker muscular dystrophy OrphaNet C1963281 Vomiting adverse event C0035439 Rheumatic heart disease HSDN C1962972 Proteinuria adverse event C3888013 Hypnoses HSDN C0080274 Retention urinary C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C1557397 Adverse event associated with pain C0013377 Dysgerminoma HSDN C1384666 Decreased hearing C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0522224 Palsied C0018817 Atrial septal defects HSDN C0036572 Convulsion C0268250 Gaucher disease, type 2 (disorder) MalaCards|HPO|UMLS C0398650 Idiopathic thrombocytopenia purpura C0020550 Hyperthyroidism HSDN C0000737 Abdomen pain C0011649 Dermoid cyst HSDN C0020649 Blood pressure decreased C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0454644 Delayed language development C0023014 Language development disorders MalaCards C0917816 Deficiency mental C0580190 3-phosphoglycerate dehydrogenase deficiency MalaCards C0030552 Paralysis partial C0342701 Transcobalamin ii deficiency MalaCards C0000737 Abdomen pain C0024620 Primary malignant neoplasm of liver MalaCards C4085317 Diarrhea frequency C0242488 Acute lung injury HSDN C1963065 Apnea adverse event C0016756 Fructose-1,6-diphosphatase deficiency MalaCards|HPO C4085317 Diarrhea frequency C0020192 Hyaline membrane disease HSDN C4084726 Distress cough C0019069 Hemophilia a HSDN C2984057 Have nausea C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C4084768 Usual severity vomiting C1864498 Renal tubular acidosis, distal, autosomal recessive MalaCards|HPO C1549543 Administration method - pain C0008698 Maxillary sinusitis chronic HSDN C3641756 Have diarrhea C3152144 Agammaglobulinemia 1, autosomal recessive HPO C4085661 Usual severity nausea C1555914 Psychologist - psychotherapy, group HSDN C4084802 Usual severity diarrhea C0162565 Acute intermittent porphyria MalaCards|HPO C4085211 Pain distress question C0340629 Aortic aneurysm without mention of rupture nos HSDN C4042891 Sleep wake disorders C1837218 Cleft palate, isolated HSDN C0004093 Asthenia C0275148 Poisoning of animal by plant HSDN C4085317 Diarrhea frequency C2239112 Blister dosing unit HSDN C0002962 Angina C1867451 Pseudoxanthoma elasticum, heterozygous HPO C0037763 Spasm C0004364 Autoimmune diseases HSDN C4084802 Usual severity diarrhea C0012546 Diphtheria HSDN C0018775 Hearing loss bilateral C0011849 Diabetes mellitus HSDN C0518090 Frequency of pain question C0006266 Bronchial spasm HSDN C0007758 Cerebellar ataxia C0042487 Venous thrombosis HSDN C1549543 Administration method - pain C0022575 Keratoconjunctivitis sicca HSDN C1263846 Attention deficit disorder with hyperactivity C0795888 Autism, susceptibility to, x-linked 4 MalaCards C0030552 Paralysis partial C0001175 Acquired immunodeficiency syndrome HSDN C4084724 Usual severity constipation C1838568 Sacral defect and anterior sacral meningocele HPO C4084774 Have weight loss C0243057 Stomatognathic system abnormalities HSDN C0557874 Global developmental delay C1846648 Microcephaly, amish type (disorder) MalaCards C0085632 Listlessness C1848914 Hexosaminidase a deficiency, adult type HPO C0036572 Convulsion C0340493 Paroxysmal familial ventricular fibrillation MalaCards C0848203 Male pelvic pain C0021831 Intestinal diseases HSDN C4085211 Pain distress question C1879338 Bereavement, life event HSDN C2132198 Abnormal blistering of the skin C1862005 Epidermolytic hyperkeratosis, late-onset HPO C0242936 Center pain C0001314 Acute disease HSDN C0007814 Cerebrospinal fluid otorrhea C0699744 Infection of ear HSDN C0349588 Stature short C1859301 Cerebellar hypoplasia with endosteal sclerosis MalaCards C0344428 Ventricular tachycardia by ecg finding C2751083 Brugada syndrome 8 MalaCards|HPO C3146279 Coma C0001433 Adenoma, acidophil HSDN C0036572 Convulsion C1864887 Cortical dysplasia-focal epilepsy syndrome HPO C0557874 Global developmental delay C0265321 Wyburn-mason syndrome OrphaNet|MalaCards C0242936 Center pain C0017563 Gingival diseases HSDN C2919142 Short stature adverse event C0795944 Fountain syndrome MalaCards C3463815 Feel fatigue C0020507 Hyperplasia HSDN C0232488 Colic C0239189 Disaccharide intolerance MalaCards C0019825 Voice hoarseness C0023804 Lipomatosis, multiple symmetrical HSDN C4085211 Pain distress question C0022610 Kernicterus HSDN C0038990 Sweats C2931542 Shapiro syndrome OrphaNet|MalaCards C0034933 Abnormal reflexes C0030353 Papilledema HSDN C0497406 Over weight C0024437 Macular degeneration HSDN C1963093 Dizziness adverse event C0015806 Femur neck fracture HSDN C0241165 Skin thickening C0151717 Hypertrophy skin UMLS C2237041 Shox gene with short stature C0078982 Arhinencephaly MalaCards C2032395 Pelvic pain on the left C0033348 Language program HSDN C1963071 Back pain adverse event C0007099 Carcinoma in situ HSDN C3539893 Pelvic pain occurs with intercourse C0009244 Behavioral cognitive therapy HSDN C4084766 Vomiting C0026785 Munchhausen syndrome HSDN C0728710 Pupil constriction observed C0026499 Monosomy HSDN C2237041 Shox gene with short stature C3150790 Chromosome 6q11-q14 deletion syndrome MalaCards C0030552 Paralysis partial C0037313 Sleep HSDN C0022346 Yellow skin C0018800 Cardiomegaly HSDN C0424755 Fever symptoms C0027726 Nephrotic syndrome HSDN C0012833 Dizzy C0030297 Pancreatic neoplasm HSDN C0027498 Nausea vomiting C2242987 Benign mastocytoma MalaCards C3541349 Syncope C0079487 Helicobacter infections HSDN C4084802 Usual severity diarrhea C0018916 Hemangioma HSDN C1963086 Confusion adverse event C0006434 Burn injury HSDN C0035229 Respiratory function impaired C0085655 Polymyositis OrphaNet|MalaCards C4085211 Pain distress question C3889576 Euphoria HSDN C0018808 Murmur C0014116 Endocardial cushion defects HSDN C0917816 Deficiency mental C1850320 Oliver syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C1548484 Rheumatic fever vaccine HSDN C0028738 Nystagmus C2930798 Alexanders leukodystrophy MalaCards C1549543 Administration method - pain C0042847 Vitamin b 12 deficiency HSDN C1000483 Genus anemia C0268412 Infantile hypophosphatasia MalaCards|HPO C1384666 Decreased hearing C0016508 Congenital foot deformity HSDN C0344315 Mood depressed C0035372 Rett syndrome OrphaNet|HPO|MalaCards C0020796 Profoundly mentally retarded C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO C0521483 Mucous hyperplasia C0023531 Leukoplakia UMLS C0020672 Body temperature decreased C0015397 Disorder of eye HSDN C1963087 Constipation adverse event C2984291 Glioblastoma multiforme pathway HSDN C0015970 Fever unknown origin C0085077 Sweet syndrome HSDN C0020305 Fetal edema C0035238 Congenital abnormality of respiratory system HSDN C0557874 Global developmental delay C1865644 Plantar lipomatosis, unusual facies, and developmental delay MalaCards|HPO C1504494 Tingling in extremities C0030554 Paresthesia UMLS C1963091 Diarrhea adverse event C0014179 Endometritis HSDN C0010200 Cough symptom C0009240 Cognition HSDN C0007758 Cerebellar ataxia C0001721 Emotional affect HSDN C0030552 Paralysis partial C0796274 Brown-vialetto-van laere syndrome OrphaNet C0037316 Not enough sleeping C0031117 Peripheral neuropathy HSDN C0043094 Weight gain C3888013 Hypnoses HSDN C2911647 Weight gain adverse event C0002453 Amenorrhea HSDN C2984058 Have pain C3150878 Hyperoxaluria, primary, type iii MalaCards C2875361 Other acute postprocedural pain C0154725 Oth disorder nervous system UMLS C0557874 Global developmental delay C1844853 Brachytelephalangic chondrodysplasia punctata HPO C0030193 Sense of pain C0237104 Spirituality HSDN C0015672 Decreased energy C0018789 Cardiac aneurysm HSDN C1279888 Proteinuria of undiagnosed cause C1970820 Fabry disease, cardiac variant HPO C0018772 Deafness C0265354 Charge syndrome OrphaNet|HSDN|HPO|MalaCards C1963091 Diarrhea adverse event C0273486 Cranial nerve x injury HSDN C0242936 Center pain C0333355 Inflammatory disease of mucous membrane HSDN C0015468 Face pain C0034931 Reflex sympathetic dystrophy HSDN C0019209 Large liver C3536715 Aa amyloidosis MalaCards C0040822 D tremors C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C3539891 Pelvic pain to the rear C0027095 Myosarcoma HSDN C0012833 Dizzy C0032816 Post-concussion headache HSDN C0231528 Muscle pain generalized C0035435 Rheumatism HSDN C1963065 Apnea adverse event C1837713 Joubert syndrome 3 MalaCards C0025323 Bleeding menstrual heavy C0010481 Cushing syndrome OrphaNet|HPO C4085210 Usual severity pain C0019065 Hemorrhage intraperitoneal HSDN C0009080 Finger clubbing C0265283 Atelosteogenesis, type 1 MalaCards|HPO C1549543 Administration method - pain C0015456 Facial dermatoses HSDN C1384666 Decreased hearing C0018939 Hematological disease HSDN C4085210 Usual severity pain C0242216 Biliary calculi HSDN C0000737 Abdomen pain C2987193 Pancreatic intraductal papillary mucinous neoplasm, intestinal-type UMLS C0034124 Pupillary disorder C3178956 Artificial intra ocular implant dislocation HSDN C0030193 Sense of pain C0231767 Achillodynia UMLS C0020578 Hyperventilate C0040128 Thyroid diseases HSDN C0030552 Paralysis partial C0700208 Acquired scoliosis HSDN C0026821 Cramp C0302892 Congenital porencephaly HSDN C0018772 Deafness C0027765 Nervous system disorder HSDN C2911645 Weight loss adverse event C0021799 Interprofessional relations HSDN C0426579 Anorexia symptom C0153463 Malig neop oth spec pancreas MalaCards C0040460 Dental pain C0011351 Dental enamel hypoplasia HSDN C0018777 Deafness, conductive C0022658 Kidney diseases HSDN C0973461 Dysphasia C0432268 Osteopathia striata cranial sclerosis MalaCards C4084776 Weight loss C0021071 Immunoproliferative small intestinal disease HSDN C1961131 Cough adverse event C0003838 Arterial occlusive diseases HSDN C0042571 Vertigo subjective C0477457 Vertig syn, dis class elsew UMLS C2237041 Shox gene with short stature C1859487 Biemond syndrome ii MalaCards C0233565 Bradykinesia C1868594 Perry syndrome MalaCards|HPO C0042024 Urine incontinence C1858106 Spastic paraplegia 12, autosomal dominant (disorder) MalaCards|HPO C4085661 Usual severity nausea C0348018 Projections HSDN C0003469 Anxiety disorder C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C0040034 Thrombocytopenia C2751686 Lymphoproliferative syndrome, ebv-associated, autosomal, 1 HPO C0948396 Frequent headache C2931196 Craniofacial dysostosis type 1 MalaCards|UMLS C3641756 Have diarrhea C0517555 Venous thrombosis after immobility HSDN C2315100 Pediatric failure to thrive C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards|HPO C0013604 Edematous C0026896 Myasthenia gravis HSDN C0042024 Urine incontinence C0041971 Tumor urethra HSDN C0018775 Hearing loss bilateral C0029396 Heterotopic ossification HSDN C1963090 Dehydration adverse event C1864498 Renal tubular acidosis, distal, autosomal recessive MalaCards|HPO C3898969 Have been vomiting C0342784 Pearson's marrow-pancreas syndrome HPO C1963086 Confusion adverse event C0032268 Pneumocephalus HSDN C0000727 Abdomen acute C3495422 Finding relating to sexuality and sexual activity HSDN C3898969 Have been vomiting C2706915 Language:-:point in time:^patient:- HSDN C0016382 Cutaneous vascular engorgement C0042109 Urticaria HSDN C0042755 Virilisation C1999266 Depression adverse event HSDN C0151889 Reflexes tendon increased C0752123 Spinocerebellar ataxia type 5 HPO C0028738 Nystagmus C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0018784 Deafness sensorineural C1275078 Acrocephalopolysyndactyly type 2 HPO C0033377 Caudal displacement C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C0042571 Vertigo subjective C0015408 Eye injury HSDN C0027796 Neuralgias C1548578 Location characteristic id - smoking HSDN C0035232 Diaphragmatic paralysis C1556061 Electric injuries HSDN C0426579 Anorexia symptom C0022758 Kap HSDN C0009806 Constipate C0278479 Stage ii colon cancer UMLS C0042963 Symptoms vomiting C3495559 Juvenile arthritis HSDN C4084768 Usual severity vomiting C1269683 Major depressive disorder HSDN C0028738 Nystagmus C1839264 Spastic paraplegia 2, x-linked (disorder) MalaCards|HPO C1557397 Adverse event associated with pain C2051831 Pectus excavatum HSDN C0013404 Respiratory difficulty C0001807 Aggressive behavior HSDN C4084776 Weight loss C0039538 Teratoma HSDN C3463815 Feel fatigue C0019195 Hepatitis, viral, human HSDN C0013911 Emaciate C0013292 Obstruction duodenal HSDN C2032395 Pelvic pain on the left C0007097 Carcinomas HSDN C0030200 Intractable pain C0158322 Calcaneus spur HSDN C0008031 Pain chest C0035435 Rheumatism HSDN C3829611 Nausea frequency C0004935 Animal ethology HSDN C0002962 Angina C0034088 Pulmonary valve insufficiency HSDN C2096293 Ent surgical result ear vertigo C3812171 Bradycardia by ecg finding HSDN C4084769 Vomiting frequency C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0009421 Comatose C0344315 Depressed mood HSDN C0024031 Back pain lower back C0043251 Wounds and injuries HSDN C4084727 Cough frequency C0243026 Sepsis HSDN C0027497 Queasy C0012979 Canine disease HSDN C0015938 Fetal macrosomia C2751824 46, xy disorders of sex development HSDN C0043094 Weight gain C0009782 Connective tissue diseases HSDN C2919142 Short stature adverse event C1704375 Hypophosphatemic rickets OrphaNet|HPO|MalaCards C1384666 Decreased hearing C1959582 Pten hamartoma tumor syndrome MalaCards C3641755 Have constipation C0024299 Lymphoma HSDN C0003862 Pain joint C0030305 Pancreatitis HSDN C3887638 Failure to thrive in infant C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency HPO C0008031 Pain chest C0040028 Thrombocythemia, essential OrphaNet|HPO|MalaCards C3829611 Nausea frequency C0007117 Basal cell carcinoma HSDN C0015672 Decreased energy C0005424 Biliary tract diseases HSDN C0018834 Brash C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C3641756 Have diarrhea C0011854 Diabetes mellitus, insulin-dependent HSDN C4084768 Usual severity vomiting C3280314 Combined malonic and methylmalonic aciduria MalaCards C0042963 Symptoms vomiting C0268151 Classical galactosemia MalaCards|HPO|UMLS C0015970 Fever unknown origin C0038539 Empyema, subdural HSDN C0424755 Fever symptoms C0017636 Glioblastoma HSDN C0042963 Symptoms vomiting C0032269 Pneumococcal infections HSDN C3665492 Pigmentations C0027766 Nervous system neoplasms MalaCards C0235031 Neurological complaint C0584995 Impaired writing UMLS C2362324 Pediatric obesity C4085635 Appetite quality question HSDN C4084723 Constipation C2713347 7-dehydrocholesterol reductase deficiency MalaCards C2919142 Short stature adverse event C0796124 Proud syndrome HPO C0030193 Sense of pain C0022573 Keratoconjunctivitis HSDN C0015938 Fetal macrosomia C0035220 Respiratory distress syndrome, newborn HSDN C4085222 Nausea C4049644 Depression HSDN C2024893 Cardiovascular surgery result: fatigue C1963134 Hemorrhoids adverse event HSDN C0023012 Delay language C2678046 Mental retardation, x-linked, syndromic, turner type OrphaNet|HPO C0015970 Fever unknown origin C1299262 Sarcoma - category (morphologic abnormality) HSDN C4085211 Pain distress question C0235146 Emotionally high HSDN C4084727 Cough frequency C0003486 Aortic aneurysm HSDN C0344434 Atrial fibrillation ecg C3808145 Left ventricular noncompaction 9 MalaCards C1963091 Diarrhea adverse event C4084839 Scabies HSDN C0018681 Headache, cephalalgia C0205770 Choroid plexus papilloma HPO|UMLS C4085317 Diarrhea frequency C0026764 Multiple myeloma HSDN C0518090 Frequency of pain question C0039240 Supraventricular tachycardia HSDN C4085642 Level of joint stiffness C1855305 Ter haar syndrome MalaCards C0018784 Deafness sensorineural C1848488 Pierre robin syndrome with fetal chondrodysplasia HPO C0460137 Push down or depress C0025268 Multiple endocrine neoplasia type 2a OrphaNet C4085317 Diarrhea frequency C0017601 Glaucomas HSDN C1962972 Proteinuria adverse event C2931788 Atypical hemolytic uremic syndrome OrphaNet|MalaCards C2237041 Shox gene with short stature C2931484 Cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation OrphaNet|MalaCards C0011991 Loose stools C0020192 Hyaline membrane disease HSDN C0557874 Global developmental delay C3150987 Epileptic encephalopathy, early infantile, 11 MalaCards|HPO C0018681 Headache, cephalalgia C1565489 Renal insufficiency HSDN C0036572 Convulsion C1321780 Hypomagnesmic tetany MalaCards C1963281 Vomiting adverse event C0010481 Cushing syndrome HSDN C3887638 Failure to thrive in infant C1384672 Hpt gene HSDN C0023015 Language handicap C0349464 Wernicke-korsakoff syndrome HSDN C2911647 Weight gain adverse event C0038013 Ankylosing spondylitis HSDN C0026821 Cramp C1568272 Tendinopathy HSDN C0015468 Face pain C0001580 Adolescent behavior HSDN C0745488 Joint erythematous painful C0023467 Leukemia, myelocytic, acute UMLS C0233565 Bradykinesia C3806722 Parkinsonism with spasticity, x-linked MalaCards|UMLS C1000483 Genus anemia C1260899 Anemia, diamond-blackfan OrphaNet|MalaCards C0151686 Growth retardation C4015344 Peroxisomal fatty acyl-coa reductase 1 disorder MalaCards C0235153 Sensory hallucination C0268631 Succinic semialdehyde dehydrogenase deficiency MalaCards|HPO C1549543 Administration method - pain C0013289 Duodenal diseases HSDN C0042024 Urine incontinence C0036916 Sexually transmitted diseases HSDN C0009806 Constipate C0796561 Melanoma vaccines HSDN C1557397 Adverse event associated with pain C3495801 Granulomatosis with polyangiitis HSDN C0151889 Reflexes tendon increased C4015505 Spinocerebellar ataxia, autosomal recessive 18 MalaCards C0042025 Urinary incontinence stress C0018944 Hematoma HSDN C0035229 Respiratory function impaired C0221759 Brachial plexus neuritis MalaCards|HPO C4084766 Vomiting C0376550 Astroviridae infection HSDN C1971624 Appetite absent C0017536 Giardiasis HSDN C3539896 Pelvic pain occurs with urination C0009373 Colonic diseases HSDN C3539890 Pelvic pain causes awakening at night C0242350 Erectile dysfunction HSDN C4084776 Weight loss C0030653 Behavior, paternal HSDN C0009676 Confusion state C0022336 Creutzfeldt-jakob disease MalaCards|HSDN|HPO C0015469 Facial paralysis C0027809 Neurilemmoma OrphaNet|MalaCards C4084788 Have dizziness C0024630 Malingering HSDN C0009676 Confusion state C0023418 Leukemia HSDN C3539895 Pelvic pain occurs with bowel movement C0004935 Animal ethology HSDN C0012569 Double vision C0007774 Cerebral arterial diseases HSDN C0028081 Night sweat C0001857 Aids related complex UMLS C0030552 Paralysis partial C0032343 Poisoning HSDN C0013404 Respiratory difficulty C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0027497 Queasy C0154723 Migraine with aura HSDN C0235153 Sensory hallucination C0220669 Familial benign neonatal epilepsy MalaCards|HPO C0497247 Blood pressure elevation C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) MalaCards|HPO C0233514 Behavior abnormal C1855995 L-2-hydroxyglutaric aciduria OrphaNet|HPO|MalaCards C4084773 Bothered by weight gain C0002880 Autoimmune hemolytic anemia HSDN C0036572 Convulsion C2673648 Hypomagnesemia 4, renal MalaCards|HPO C0019079 Bloody sputum C0206694 Mucoepidermoid carcinoma HSDN C4084727 Cough frequency C0022758 Kap HSDN C0231835 Respiration rate increased C0852283 Respiratory distress syndrome MalaCards C0518090 Frequency of pain question C0023787 Lipodystrophy HSDN C4084769 Vomiting frequency C2711591 Infection by anisakidae HSDN C3539895 Pelvic pain occurs with bowel movement C0233894 Femininity HSDN C0007814 Cerebrospinal fluid otorrhea C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0853986 Lymphocytes decreased C0024215 Lymphangiectasis, intestinal OrphaNet|MalaCards C0237326 Defecation pain C0043207 Wolfram syndrome MalaCards|HPO C0020578 Hyperventilate C0149931 Migraine disorders HSDN C2919142 Short stature adverse event C0029089 Ophthalmoplegia MalaCards C0878773 Bladder hyperactive C0033923 Psychomotor function HSDN C2911645 Weight loss adverse event C0007570 Celiac disease HSDN C0007758 Cerebellar ataxia C1956391 Temporal arteritis MalaCards|HPO C3641755 Have constipation C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C1557397 Adverse event associated with pain C0556482 Protection sex HSDN C1557397 Adverse event associated with pain C0013589 Ectromelia HSDN C2315100 Pediatric failure to thrive C1844887 Catel manzke syndrome OrphaNet|HPO|MalaCards C0019079 Bloody sputum C0020517 Hypersensitivity HSDN C0349588 Stature short C0026363 Mohr-claussen syndrome MalaCards C4084767 Bothered by vomiting C0014836 Escherichia coli infections HSDN C3829611 Nausea frequency C3541306 Plasmodium measurement HSDN C1963091 Diarrhea adverse event C0008775 Ciguatera poisoning HSDN C0042798 Vision dim C0236969 Substance-related disorders HSDN C4084723 Constipation C0085258 Deficiency, yang HSDN C0004093 Asthenia C1881674 Medical device emits smoke HSDN C0018772 Deafness C0033817 Pseudomonas infections HSDN C1963281 Vomiting adverse event C0042035 Urination disorders HSDN C1963281 Vomiting adverse event C0024141 Lupus erythematosus, systemic HSDN C0231218 Malaise generalized C1336418 Hepatocellular cancer stage iv ajcc v6 UMLS C0454644 Delayed language development C0796215 Mental retardation, x-linked 9 HPO C4085317 Diarrhea frequency C0016952 Galactosemias MalaCards C0024032 Birth weight subnormal C1857555 Hsd11b2, arg337cys HPO C4084726 Distress cough C0036974 Shock HSDN C0035229 Respiratory function impaired C0027877 Neuronal ceroid-lipofuscinoses OrphaNet|MalaCards C4085210 Usual severity pain C0020621 Hypokalemia HSDN C4085210 Usual severity pain C0242188 Spider bites HSDN C1549543 Administration method - pain C0024638 Class ii division 2 malocclusion HSDN C0033774 Skin pruritus C1843116 Bile acid synthesis defect, congenital, 1 MalaCards|HPO C4084766 Vomiting C0155866 Inhalational anthrax OrphaNet|MalaCards C0019209 Large liver C3553607 Mitochondrial pyruvate carrier deficiency MalaCards C0518090 Frequency of pain question C1321581 Bezoar disorder HSDN C0018991 Paralysis one side of body C0025007 Measles HSDN C0424755 Fever symptoms C0085257 Yin deficiency HSDN C3541349 Syncope C0152171 Idiopathic pulmonary hypertension OrphaNet C0034150 Skin purpura C2004487 Vaginal spasm HSDN C3463815 Feel fatigue C2911643 Encounter due to family history of osteoporosis HSDN C0522224 Palsied C0015745 Ingestive behavior HSDN C3829611 Nausea frequency C0007527 Cecal disease HSDN C0027066 Myoclonic jerking C0393702 Myoclonic astatic epilepsy MalaCards|HPO C4084776 Weight loss C0010054 Coronary arteriosclerosis HSDN C1557397 Adverse event associated with pain C0021845 Intestinal perforation HSDN C0349588 Stature short C1846059 Roifman syndrome MalaCards C4084724 Usual severity constipation C0039590 Testicular neoplasms HSDN C0018784 Deafness sensorineural C0020619 Hypogonadism HSDN C4085317 Diarrhea frequency C0038271 Stereotyped behavior HSDN C0036572 Convulsion C1857662 Coach syndrome MalaCards|HPO C0019209 Large liver C0085280 Alagille syndrome OrphaNet C1963093 Dizziness adverse event C0027051 Myocardial infarction HSDN C4085862 Bothered by nausea C0035204 Respiration disorders HSDN C1557397 Adverse event associated with pain C0423772 Cutaneous fistula HSDN C4084726 Distress cough C0867389 Chronic graft-versus-host disease MalaCards C0349588 Stature short C0026760 Multiple epiphyseal dysplasia OrphaNet|MalaCards C0042571 Vertigo subjective C0155519 Labyrinth reactiv.loss-unilat. UMLS C0043068 Friderichsen-waterhouse syndrome C0398625 Protein c deficiency HSDN C4085661 Usual severity nausea C0033054 Prenatal exposure delayed effects HSDN C0232466 Feeding difficulty C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO C0010200 Cough symptom C1708792 Lymphoepithelioma-like lung carcinoma UMLS C2984058 Have pain C0018081 Gonorrhea HSDN C0917816 Deficiency mental C0796033 Marden-walker syndrome MalaCards|HPO C0917816 Deficiency mental C0795822 8 rec syndrome OrphaNet|MalaCards C3146279 Coma C0003492 Aortic coarctation HSDN C4084773 Bothered by weight gain C0011311 Dengue fever HSDN C0002170 Alopecia disorders C0432313 Epidermolysis bullosa simplex with hypodontia OrphaNet|MalaCards C0030200 Intractable pain C0016658 Fracture bone HSDN C0012833 Dizzy C0034088 Pulmonary valve insufficiency HSDN C0018772 Deafness C0021890 Intraoperative complications HSDN C4084774 Have weight loss C0162557 Liver failure, acute HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0860603 Anxiety symptoms HSDN C2919142 Short stature adverse event C1848862 Miller-mckusick-malvaux-syndrome (3m syndrome) OrphaNet|HPO C0016199 Pain flank C0278678 Metastatic renal cell cancer UMLS C1963137 Hydrocephalus adverse event C1854108 Cerebrooculonasal syndrome MalaCards C0009080 Finger clubbing C0085404 Poems syndrome MalaCards C1961131 Cough adverse event C0012546 Diphtheria HSDN C3898969 Have been vomiting C0035222 Respiratory distress syndrome, adult HSDN C4084723 Constipation C0018133 Graft-vs-host disease HSDN C0009806 Constipate C0810319 Other and unspecified gastrointestinal disorders UMLS C3539023 Pelvic pain increasing in frequency C0020517 Hypersensitivity HSDN C4085642 Level of joint stiffness C0282193 Iron overload OrphaNet C2024878 Cardiovascular surgery result: dyspnea C0027051 Myocardial infarction HSDN C0009421 Comatose C0021368 Inflammation HSDN C2024893 Cardiovascular surgery result: fatigue C0029118 Opportunistic infections HSDN C0522224 Palsied C0206648 Myofibromatosis HSDN C0003862 Pain joint C0376620 Pouchitis HSDN C0013395 Indigestion C0018798 Congenital heart defects HSDN C2024878 Cardiovascular surgery result: dyspnea C1414899 Gaa gene HSDN C3887638 Failure to thrive in infant C0026709 Mucopolysaccharidosis vi OrphaNet|MalaCards C0041657 Consciousness loss C0027407 Narcotherapy HSDN C0011991 Loose stools C0424688 Small head HSDN C1860844 Sparse, thin hair C1839321 Scarf syndrome MalaCards C3463815 Feel fatigue C0001624 Adrenal gland neoplasms HSDN C0037036 Increased salivation C1859807 Amyotrophic lateral sclerosis 2, juvenile (disorder) MalaCards|HPO C3815497 Cough C0018944 Hematoma HSDN C0398650 Idiopathic thrombocytopenia purpura C0042373 Vascular diseases HSDN C2911645 Weight loss adverse event C0004364 Autoimmune diseases HSDN C0439029 Deafness symptom C2106542 Combined hearing and vision loss with deafness UMLS C0162298 Stiffness joints C0175700 Multiple synostosis syndrome MalaCards C0277959 Hair coarseness C1848435 Arwh1 MalaCards|HPO C0019209 Large liver C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C0022346 Yellow skin C1962971 Myocarditis adverse event HSDN C0497247 Blood pressure elevation C1861457 Progressive encephalomyelitis with rigidity MalaCards C0013604 Edematous C0085404 Poems syndrome MalaCards|HSDN C1963087 Constipation adverse event C2713392 Phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency HPO C3665347 Vision impaired C0338503 Septo-optic dysplasia OrphaNet|HPO C0917816 Deficiency mental C0035921 Congenital rubella syndrome OrphaNet|MalaCards C1963091 Diarrhea adverse event C1443900 Inhalational botulism OrphaNet|MalaCards C0042963 Symptoms vomiting C0002880 Autoimmune hemolytic anemia HSDN C4084802 Usual severity diarrhea C0238124 Necrotizing fasciitis HSDN C0751401 Ophthalmoparesis C1837092 Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency HPO C0010520 Skin cyanosis C0025063 Mediastinal neoplasms HSDN C2242996 Tingling C0027651 Tumor HSDN C4084773 Bothered by weight gain C0014852 Esophageal diseases HSDN C0349588 Stature short C1845243 Mental retardation, x-linked, syndromic, claes-jensen type OrphaNet|HPO|MalaCards C3665346 Loss sight C0003076 Aniridia OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0241158 Cicatrix skin HSDN C3539893 Pelvic pain occurs with intercourse C0024141 Lupus erythematosus, systemic HSDN C0018681 Headache, cephalalgia C0700208 Acquired scoliosis HSDN C0036572 Convulsion C0265987 Nevus comedonicus MalaCards|HPO C0151825 Ostalgia C4085252 Paget disease of bone 3 UMLS C0234132 Pyramidal sign C0520719 Spinopontine atrophy MalaCards C0557874 Global developmental delay C2752074 Alpha-ketoglutarate dehydrogenase deficiency OrphaNet|HPO|MalaCards C1279888 Proteinuria of undiagnosed cause C2930923 N-acetylneuraminic acid storage disease MalaCards C0015970 Fever unknown origin C0035021 Relapsing fever HSDN C0013604 Edematous C0014170 Endometrial neoplasms HSDN C0013404 Respiratory difficulty C0022116 Ischemia HSDN C0020673 Hypothermia (central) (local) C0033968 Psychotherapeutic technique HSDN C0027066 Myoclonic jerking C1856491 Gaucher disease, type iiia HPO C2315100 Pediatric failure to thrive C0016065 Polyostotic fibrous dysplasia HSDN C3539889 Pelvic pain increasing in severity C0023890 Liver cirrhosis HSDN C4084776 Weight loss C0006818 Campylobacter infection HSDN C0151827 Pain eye C0027858 Neuroma HSDN C0011206 Delirium acute C0022658 Kidney diseases HSDN C1961131 Cough adverse event C0005586 Bipolar disorder HSDN C0036572 Convulsion C1854335 Epilepsy, nocturnal frontal lobe, type 3 MalaCards|HPO C4084725 Usual severity cough C0051981 Anti-leprosy vaccine HSDN C2237041 Shox gene with short stature C0796002 Johnson-mcmillin syndrome MalaCards C0036572 Convulsion C0268630 Hyper-beta-alaninemia MalaCards C3887873 Hearing loss C0314657 Genetic predisposition HSDN C1860844 Sparse, thin hair C1327916 Revesz syndrome (disorder) MalaCards|HPO C4084769 Vomiting frequency C0041374 Tumor virus infections HSDN C3274924 Have been coughing C0004935 Animal ethology HSDN C0268988 Itch penis C0030846 Penile diseases UMLS C0035455 Rhinitis C0042111 Urticaria pigmentosa OrphaNet|MalaCards C2911645 Weight loss adverse event C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0030193 Sense of pain C0024523 Malabsorption syndrome HSDN C0015230 Exanthem C0041834 Erythema UMLS C0036572 Convulsion C3279738 Cerebral palsy, spastic quadriplegic, 5, formerly MalaCards|UMLS C3539891 Pelvic pain to the rear C0025202 Melanoma HSDN C0040485 Wryneck C0810353 Other back pain and disorders UMLS C0018834 Brash C1458155 Mammary neoplasms HSDN C0013604 Edematous C0027746 Nerve degeneration HSDN C0015469 Facial paralysis C1704972 Genomic orientation HSDN C4085317 Diarrhea frequency C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C0042024 Urine incontinence C0393590 Fahr's syndrome (disorder) MalaCards|HPO C0234376 Tremor action C1866398 Proteus-like syndrome (disorder) MalaCards|HPO C0020538 Hbp C0342739 Trimethylaminuria MalaCards|HPO C0030193 Sense of pain C0600041 Infective cystitis HSDN C1963091 Diarrhea adverse event C0028945 Oligodendroglioma HSDN C1279888 Proteinuria of undiagnosed cause C0002792 Anaphylaxis HSDN C1546759 Specimen source codes - pustule C0221036 Acrodermatitis enteropathica OrphaNet|HPO C0427055 Face weakness C3648312 Late effects of cerebral infarction facial weakness UMLS C4084725 Usual severity cough C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0014356 Enterocolitis HSDN C0026838 Spasticity muscle C0013295 Duodenal ulcer HSDN C0518090 Frequency of pain question C0006430 Burning mouth syndrome HSDN C0017565 Gingiva hemorrhage C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C4085862 Bothered by nausea C0038013 Ankylosing spondylitis HSDN C1963091 Diarrhea adverse event C0149778 Soft tissue infections HSDN C0150045 Urinary incontinence urge C2364172 Adherence to medication regime HSDN C0013362 Dysarthrias C0026613 Motor skills disorders HSDN C1963093 Dizziness adverse event C0750929 Arnold-chiari malformation, type i MalaCards C4084768 Usual severity vomiting C0020579 Hypervitaminosis a HSDN C0015672 Decreased energy C2609414 Acute kidney injury HSDN C0332563 Papulae C1851481 Erythrokeratodermia with ataxia OrphaNet|HPO C0037036 Increased salivation C1968551 Mental retardation, x-linked 79 MalaCards|HPO C0042798 Vision dim C3665342 Progressive cone dystrophy MalaCards C0043094 Weight gain C0021390 Inflammatory bowel diseases HSDN C2984058 Have pain C1548485 Rift valley fever vaccine HSDN C0002622 Amnesias C0007820 Cerebrovascular disorders HSDN C0242936 Center pain C0040247 Tinea HSDN C0018772 Deafness C0037315 Sleep apnea syndromes HSDN C2032395 Pelvic pain on the left C0227791 Discharge vaginal HSDN C0012569 Double vision C0750929 Arnold-chiari malformation, type i MalaCards C2024893 Cardiovascular surgery result: fatigue C1879338 Bereavement, life event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007785 Cerebral infarction HSDN C2203646 Jaundice C0041296 Tuberculosis HSDN C0030552 Paralysis partial C0027666 Neoplasms, radiation-induced HSDN C0028961 Urine output decreased C0220981 Metabolic acidosis HSDN C1963066 Joint pain adverse event C3540852 Rickets, x-linked hypophosphatemic MalaCards C1963137 Hydrocephalus adverse event C1853554 Radiation induced meningioma MalaCards C1519353 Skin eruption papular C0024899 Mastocytosis MalaCards C0041105 Jaw spasm C0027095 Myosarcoma HSDN C2203646 Jaundice C0034184 Pyelocystitis HSDN C3496180 Sleep apnea C1096902 Infantile sialic acid storage disease MalaCards C1963281 Vomiting adverse event C0042133 Uterine fibroids HSDN C1961131 Cough adverse event C0001122 Acidosis HSDN C4084776 Weight loss C0011603 Dermatitis HSDN C2024893 Cardiovascular surgery result: fatigue C0033975 Psychotic disorders HSDN C0002965 Crescendo angina C0037286 Skin neoplasms HSDN C0015230 Exanthem C0036285 Scarlet fever UMLS C4084776 Weight loss C0024305 Lymphoma, non-hodgkin HSDN C1557397 Adverse event associated with pain C0085094 Head injury closed HSDN C3898969 Have been vomiting C2748608 Lead poisoning, susceptibility to HPO C1963091 Diarrhea adverse event C0026848 Myopathy HSDN C1963252 Tremor adverse event C0428953 Ecg infarction myocardial HSDN C0037763 Spasm C0003803 Arnold chiari malformation HSDN C0242670 Chronic vegetative state C3245466 Observationvalue - trust HSDN C4084775 Usual severity weight loss C0032131 Plasmacytoma HSDN C0026838 Spasticity muscle C0031117 Peripheral neuropathy HSDN C0004134 Dyssynergia C1845862 Creatine deficiency, x-linked OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0024954 Maxillary neoplasms HSDN C1963170 Hypothermia adverse event C0038587 Substance withdrawal syndrome HSDN C1963091 Diarrhea adverse event C0031142 Peritoneal diseases HSDN C0009676 Confusion state C0270639 Lateral sinus thrombosis HSDN C4084727 Cough frequency C0007273 Carotid artery diseases HSDN C0040485 Wryneck C0013386 Dyskinesia, drug-induced HSDN C2984058 Have pain C0085409 Polyendocrinopathies, autoimmune HSDN C0022107 Fussiness C1836148 Supranuclear palsy, progressive, 2 MalaCards C2984057 Have nausea C0042384 Vasculitis HSDN C0042571 Vertigo subjective C0042594 Vestibular diseases UMLS C0007166 Cardiac output decreased C0002726 Amyloidosis HSDN C0018681 Headache, cephalalgia C1735856 Migraine with typical aura UMLS C4085211 Pain distress question C0271650 Impaired glucose tolerance HSDN C0750394 Wbc low C3266026 Autoimmune polyendocrine syndrome type 4 MalaCards C2984058 Have pain C0037354 Smallpox HSDN C3146279 Coma C0037929 Spinal cord injuries HSDN C1304408 Urticarial vasculitis C0301918 Hypersensitivity reaction mediated by immune complex UMLS C0003811 Cardiac rhythm disturbance C0007932 Chagas' disease + no organ inv MalaCards C0015672 Decreased energy C0008479 Chondrosarcoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011303 Demyelinating diseases HSDN C0518090 Frequency of pain question C0019156 Hepatic veno-occlusive disease HSDN C4084775 Usual severity weight loss C0206172 Diabetic foot HSDN C0151686 Growth retardation C2676137 Diamond-blackfan anemia 1 MalaCards C0349506 Sun sensitivity C1955934 Trichothiodystrophy syndromes MalaCards C0030193 Sense of pain C1879758 Atypical medullary breast carcinoma UMLS C0035078 Failure kidney C1865270 Bartter syndrome, type 4a HPO C3887638 Failure to thrive in infant C1863236 Scid due to ada deficiency, early-onset HPO C0497406 Over weight C0023418 Leukemia HSDN C4084723 Constipation C0003469 Anxiety disorders HSDN C0018681 Headache, cephalalgia C0025063 Mediastinal neoplasms HSDN C0020903 Illusion C0175702 Williams syndrome HSDN C0036572 Convulsion C0024894 Mastitis HSDN C2237041 Shox gene with short stature C0041408 Turner syndrome OrphaNet|MalaCards C0003469 Anxiety disorder C1865926 Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) MalaCards C3829611 Nausea frequency C0014118 Endocarditis HSDN C0043094 Weight gain C0342337 Insulin resistance syndrome, type b MalaCards C0162298 Stiffness joints C2931129 Ellis yale winter syndrome MalaCards C1963184 Nystagmus adverse event C0751664 Canavan disease, neonatal MalaCards C0042024 Urine incontinence C0042338 Herpesvirus 3, human HSDN C0015300 Ocular proptosis C0023787 Lipodystrophy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0003460 Anurias HSDN C2073625 X-ray of chest: pleural effusion C1867396 Radial-renal syndrome MalaCards C0000737 Abdomen pain C0029051 Oophoritis HSDN C0041667 Low weight C1842687 Pontocerebellar hypoplasia type 3 (disorder) MalaCards|HPO C4084802 Usual severity diarrhea C0002880 Autoimmune hemolytic anemia HSDN C4084776 Weight loss C0206634 Liposarcoma, myxoid MalaCards C4085548 Usual severity dizziness C1306759 Eosinophilic disorder HSDN C0018772 Deafness C0036439 Scoliosis, unspecified HSDN C0009806 Constipate C0032927 Precancerous conditions HSDN C0426579 Anorexia symptom C0024141 Lupus erythematosus, systemic HSDN C4085211 Pain distress question C1720830 Painful bladder syndrome OrphaNet|MalaCards C3898969 Have been vomiting C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C0018772 Deafness C0018817 Atrial septal defects HSDN C0240682 Pelvic girdle pain C0015806 Femur neck fracture HSDN C0242936 Center pain C3812171 Bradycardia by ecg finding HSDN C3898969 Have been vomiting C1856401 Etfa deficiencies HPO C0022346 Yellow skin C0021841 Intestinal neoplasms HSDN C0030554 Abnormal sensation C1956390 Cranial arteritis MalaCards C0522224 Palsied C0043121 Wernicke encephalopathy HSDN C0522224 Palsied C0752191 Central nervous system schistosomiasis HSDN C0033377 Caudal displacement C0265241 Franceschetti-klein syndrome MalaCards C0042798 Vision dim C0024523 Malabsorption syndrome MalaCards C0038990 Sweats C1706595 Pachyonychia congenita, jadassohn lewandowsky type MalaCards C4084802 Usual severity diarrhea C0007130 Mucinous adenocarcinoma HSDN C4085549 Dizziness C0035304 Retinal degeneration HSDN C2024893 Cardiovascular surgery result: fatigue C0237873 Physiological sexual disorders HSDN C0013421 Dystonia C0018798 Congenital heart defects HSDN C1962956 Flatulence adverse event C1963138 Hypertension adverse event HSDN C4084775 Usual severity weight loss C0346647 Malignant neoplasm of pancreas MalaCards C0018784 Deafness sensorineural C0034186 Pyelonephritis HSDN C0235162 Difficult sleeping C4225351 White-sutton syndrome UMLS C0750937 Appendicular ataxia C1527231 Adrenomyeloneuropathy MalaCards|HPO C0028738 Nystagmus C1853100 Cerebrooculofacioskeletal syndrome 4 MalaCards|HPO C0009421 Comatose C0751891 Hemorrhage, hypertensive intracranial HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0019099 Hemorrhagic fever, crimean MalaCards C2108113 Continuous electrocardiogram ventricular tachycardia C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards|HPO C0016199 Pain flank C1336314 Stage ii renal pelvis and ureter cancer UMLS C4085211 Pain distress question C0033595 Prostitution HSDN C0028738 Nystagmus C3683483 Autosomal recessive cerebellar ataxia type 1 MalaCards C0028738 Nystagmus C3502492 Microcephaly with chorioretinopathy, autosomal recessive OrphaNet|HPO|MalaCards C0030552 Paralysis partial C1838657 Vitamin d hydroxylation-deficient rickets, type 1b HPO C0413252 Hypothermia due to exposure C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C1549543 Administration method - pain C0151814 Coronary occlusion HSDN C0030486 Extremity paralysis, lower C0006840 Candidiasis HSDN C4042891 Sleep wake disorders C0023473 Myeloid leukemia, chronic HSDN C4084767 Bothered by vomiting C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0751837 Gait ataxic C0016719 Friedreich ataxia HPO C2024893 Cardiovascular surgery result: fatigue C1457883 Aggressive reaction HSDN C0042798 Vision dim C0078917 Albinism, ocular OrphaNet C0850758 Pain pelvic C0001580 Adolescent behavior HSDN C2029884 Hearing loss by exam C1855652 Fetus small for gestational age HSDN C4085317 Diarrhea frequency C0016154 Fish disease HSDN C3887638 Failure to thrive in infant C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0013395 Indigestion C0009375 Colonic neoplasms HSDN C4085317 Diarrhea frequency C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C0018991 Paralysis one side of body C0007097 Carcinomas HSDN C0424755 Fever symptoms C0153065 Eastern equine encephalomyelitis HSDN C0033774 Skin pruritus C1457883 Aggressive reaction HSDN C2203646 Jaundice C0027439 Nasopharyngeal neoplasms HSDN C0000737 Abdomen pain C0278480 Stage iii colon cancer UMLS C0028081 Night sweat C1336297 Stage ii hodgkin's disease lymphocyte depletion type UMLS C0231528 Muscle pain generalized C0009400 Colorado tick fever DiseaseOntology|MalaCards C0003962 Ascites C0040560 Toxoplasmosis, congenital MalaCards C3463815 Feel fatigue C0022658 Kidney diseases HSDN C0028961 Urine output decreased C0344315 Depressed mood HSDN C4084776 Weight loss C0003504 Aortic valve insufficiency HSDN C0151825 Ostalgia C0014084 Enchondromatosis OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0085183 Neoplasms, second primary HSDN C0030193 Sense of pain C0022882 Infection laboratory HSDN C4084773 Bothered by weight gain C0035455 Rhinitis HSDN C0036572 Convulsion C0015732 Fecal incontinence HSDN C0018524 Hallucinate C0041296 Tuberculosis HSDN C4049644 Depression C0342442 Acth-dependent cushing's syndrome OrphaNet C4084766 Vomiting C0012746 Dissociative disorder HSDN C0018784 Deafness sensorineural C0029456 Osteoporosis HSDN C3463815 Feel fatigue C0026760 Multiple epiphyseal dysplasia DiseaseOntology|MalaCards C0026838 Spasticity muscle C0027073 Myofascial pain syndromes HSDN C1549543 Administration method - pain C2350019 Solitary pulmonary nodule HSDN C1962972 Proteinuria adverse event C0017563 Gingival diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0009766 Allergic conjunctivitis HSDN C0424755 Fever symptoms C0276289 Zika virus infection MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0233629 Thinking and speaking disturbances HSDN C0518090 Frequency of pain question C0011253 Delusions HSDN C3274924 Have been coughing C1261473 Sarcoma HSDN C0152227 Tearing excessive C1318020 Stromal keratitis OrphaNet|MalaCards C4084726 Distress cough C0036864 Sexual relations HSDN C0018784 Deafness sensorineural C3665333 Keratitis-ichthyosis-deafness syndrome OrphaNet|HPO|MalaCards C2203646 Jaundice C0003869 Arthritis, infectious HSDN C3887638 Failure to thrive in infant C0011175 Dehydration HSDN C0221166 Paraparesis C0038017 Congenital spondylolisthesis HSDN C1963184 Nystagmus adverse event C0029534 Other cerebellar ataxia MalaCards C0398650 Idiopathic thrombocytopenia purpura C0042338 Herpesvirus 3, human HSDN C2919142 Short stature adverse event C1838162 Mesomelia-synostoses syndrome MalaCards C0035232 Diaphragmatic paralysis C3489393 Hiatal hernia HSDN C0424755 Fever symptoms C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C2911643 Encounter due to family history of osteoporosis HSDN C0036572 Convulsion C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C0000727 Abdomen acute C0019209 Hepatomegaly HSDN C1279888 Proteinuria of undiagnosed cause C0035304 Retinal degeneration HSDN C0231341 Aging premature C0524851 Neurodegenerative disorders HSDN C0518090 Frequency of pain question C0033595 Prostitution HSDN C4084775 Usual severity weight loss C0035126 Reperfusion injury HSDN C0027497 Queasy C0031039 Effusion pericardial HSDN C2911647 Weight gain adverse event C0042109 Urticaria HSDN C0522224 Palsied C0497327 Dementia HSDN C0242936 Center pain C0024419 Waldenstrom macroglobulinemia HSDN C4084766 Vomiting C0518450 Spinal fractures HSDN C2024893 Cardiovascular surgery result: fatigue C0162316 Iron deficiency anemia HSDN C2024878 Cardiovascular surgery result: dyspnea C0019054 Hemolysis (disorder) HSDN C0000731 Abdomen distention C0220685 Achondrogenesis type 2 OrphaNet|HPO C4085642 Level of joint stiffness C0024445 Lipomatosis, familial benign cervical OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0039082 Syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040961 Tricuspid valve insufficiency HSDN C4042891 Sleep wake disorders C0010054 Coronary arteriosclerosis HSDN C0004604 Pain back C1444199 Alkaptonuric ochronosis MalaCards C0010200 Cough symptom C0236969 Substance-related disorders HSDN C2024893 Cardiovascular surgery result: fatigue C2986550 Pituicytoma MalaCards C0000737 Abdomen pain C1333977 Hepatitis b virus-related hepatocellular carcinoma UMLS C0015672 Decreased energy C0027658 Neoplasms, germ cell and embryonal HSDN C3641756 Have diarrhea C0022602 Actinic keratosis HSDN C0241137 Skin pallor C0391817 Drug-induced autoim haem anaem OrphaNet|MalaCards C0002962 Angina C1963282 Wolff-parkinson-white syndrome adverse event HSDN C0018524 Hallucinate C0339534 Usher syndrome type 2 MalaCards|HPO C0043068 Friderichsen-waterhouse syndrome C0040053 Thrombosis HSDN C0031911 Pigment deposition C0334588 Giant cell glioblastoma MalaCards C0018681 Headache, cephalalgia C1334434 Lower clivus meningioma UMLS C4084784 Diarrhea C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0007859 Pain neck C0038941 Incisional infection HSDN C1557397 Adverse event associated with pain C1299919 Enteric coccidiosis HSDN C0016382 Cutaneous vascular engorgement C3693482 Giant cell fibroblastoma MalaCards C4084766 Vomiting C0035361 Pneumoretroperitoneum HSDN C0010038 Corneal opacity disorder C0853240 Mobius ii syndrome OrphaNet|HPO|MalaCards C1963086 Confusion adverse event C1556682 Adverse event associated with infection HSDN C0026826 High muscle tone C2749560 Methemoglobinemia, type ii HPO C3463815 Feel fatigue C0035228 Respiratory hypersensitivity HSDN C0587047 Mass of trunk C0344044 Ascaris peritoneal granuloma UMLS C1565249 Limitation, mobility C0023676 Life style HSDN C3665347 Vision impaired C3809482 Myopia 23, autosomal recessive MalaCards C2024893 Cardiovascular surgery result: fatigue C0080040 Polio post syndrome MalaCards C0427055 Face weakness C0410203 X-linked centronuclear myopathy HPO|UMLS C0034150 Skin purpura C0024421 Macroglossia HSDN C0018784 Deafness sensorineural C0016658 Fracture bone HSDN C2919142 Short stature adverse event C0010314 Cri-du-chat syndrome OrphaNet|HPO|MalaCards C0016382 Cutaneous vascular engorgement C1857449 Cutaneous photosensitivity and colitis, lethal MalaCards C4084768 Usual severity vomiting C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C0557874 Global developmental delay C2674574 Aortic aneurysm, familial thoracic 3 MalaCards C3665346 Loss sight C0268344 Ehlers-danlos syndrome 6b OrphaNet|UMLS|HPO|MalaCards C1557397 Adverse event associated with pain C0022680 Polycystic kidney diseases HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0042514 Tachycardia, ventricular HSDN C0398650 Idiopathic thrombocytopenia purpura C0520946 Emotional hypersensitivity HSDN C0018772 Deafness C0870082 Hyperkeratosis HSDN C4085317 Diarrhea frequency C0013922 Embolism HSDN C2315100 Pediatric failure to thrive C2984299 Asthma pathway HSDN C0019079 Bloody sputum C0023886 Liver abscess, amebic HSDN C2029884 Hearing loss by exam C0026918 Mycobacterium infections HSDN C0039070 Collapse fleeting C1832680 Cardiomyopathy, dilated, 1e MalaCards|HPO|UMLS C0023380 Lethargy C3887523 Very long chain acyl-coa dehydrogenase deficiency UMLS C0013404 Respiratory difficulty C0947622 Cholecystolithiasis HSDN C0234523 Apraxia, classic C0085215 Ovarian failure, premature HSDN C4084723 Constipation C2931294 Wiedemann grosse dibbern syndrome MalaCards C2911647 Weight gain adverse event C0021841 Intestinal neoplasms HSDN C1963252 Tremor adverse event C0034063 Pulmonary edema HSDN C0010038 Corneal opacity disorder C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0036899 Abstinence sex HSDN C0518090 Frequency of pain question C2698017 Cdisc sdtm marital status terminology HSDN C0085593 Chill C0040127 Thyroid crisis HSDN C0242936 Center pain C0008309 Bile duct adenoma HSDN C1069915 Vertigo C1838701 Deafness, autosomal recessive 2 MalaCards|HPO C0042571 Vertigo subjective C0796561 Melanoma vaccines HSDN C0043094 Weight gain C0151699 Intracranial hemorrhages HSDN C3541349 Syncope C1864850 Arrhythmogenic right ventricular dysplasia, familial, 11 HPO C0231528 Muscle pain generalized C0035613 Rift valley fever OrphaNet|MalaCards C0036396 Sciatica C0456892 Csf low pressure HSDN C0030232 Color loss C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0036572 Convulsion C0015671 Father HSDN C0028738 Nystagmus C0271097 Usher syndrome MalaCards C0243026 Generalized infection C3661523 Congenital intestinal aganglionosis MalaCards|HPO C0085593 Chill C0024788 Green monkey virus disease DiseaseOntology|MalaCards C3815497 Cough C0009651 Conditioning operant HSDN C0015672 Decreased energy C0006145 Breast diseases HSDN C0013395 Indigestion C0004623 Bacterial infections HSDN C4049602 Hyperactivity C0043379 Xyy karyotype OrphaNet C0042024 Urine incontinence C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy HPO C0427190 Ataxia, truncal C0010964 Dandy-walker syndrome MalaCards C3665492 Pigmentations C0206663 Neuroectodermal tumor, primitive MalaCards C4082202 Sleep quality question C3150674 Chromosome 15q24 deletion syndrome MalaCards C0424755 Fever symptoms C0014175 Endometriosis HSDN C1557397 Adverse event associated with pain C0032087 Plant poisoning HSDN C4085210 Usual severity pain C0271650 Impaired glucose tolerance HSDN C0040822 D tremors C0010054 Coronary arteriosclerosis HSDN C0473384 Edema or excessive weight gain in pregnancy without mention of hypertension, delivered with mention of postpartum complication C0810337 Other and unspecified complications of pregnancy UMLS C0020538 Hbp C1449844 Pseudohypoaldosteronism, type ii OrphaNet|MalaCards C4084774 Have weight loss C0014848 Esophageal achalasia HSDN C2911647 Weight gain adverse event C0035228 Respiratory hypersensitivity HSDN C4085210 Usual severity pain C0349622 Hemangiopericytoma of meninges HSDN C0406671 Burning scrotum C3839897 Disorder of skin of scrotum UMLS C0030193 Sense of pain C0206180 Ki-1+ anaplastic large cell lymphoma HSDN C1549543 Administration method - pain C0024841 Matrimony, matrimonial HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027726 Nephrotic syndrome HSDN C4084723 Constipation C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C0006370 Bulimia C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C0018784 Deafness sensorineural C0041755 Adverse reaction to drug HSDN C0026838 Spasticity muscle C0241158 Cicatrix skin HSDN C0011206 Delirium acute C0243010 Viral encephalitis HSDN C0454644 Delayed language development C1848413 Trichothiodystrophy, type 1 MalaCards C4085210 Usual severity pain C0036220 Kaposi sarcoma HSDN C0013604 Edematous C3813607 Infantile gastroesophageal reflux HSDN C2919142 Short stature adverse event C3711387 Autosomal recessive primary microcephaly OrphaNet|HPO|MalaCards C0030486 Extremity paralysis, lower C1962986 Glaucoma adverse event HSDN C0002622 Amnesias C0006277 Bronchitis HSDN C3641756 Have diarrhea C0003838 Arterial occlusive diseases HSDN C4084726 Distress cough C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive OrphaNet|MalaCards C4085317 Diarrhea frequency C0038587 Substance withdrawal syndrome HSDN C1963249 Tinnitus adverse event C0020517 Hypersensitivity HSDN C0035232 Diaphragmatic paralysis C3714644 Thymus neoplasms OrphaNet|HSDN|MalaCards C1384666 Decreased hearing C0796092 Oculo-cerebro-cutaneous syndrome MalaCards C0013404 Respiratory difficulty C0030286 Pancreatic diseases HSDN C0008031 Pain chest C0031085 Periodontal abscess HSDN C0026838 Spasticity muscle C0026975 Myelitis HSDN C4085317 Diarrhea frequency C0027430 Nasal polyps HSDN C0018772 Deafness C0242422 Parkinsonian disorders HSDN C1963249 Tinnitus adverse event C0004933 Behavior modification technique HSDN C0042571 Vertigo subjective C0009395 Color perception HSDN C0024031 Back pain lower back C0031149 Peritoneal neoplasms HSDN C0236000 Jaw bone pain C0155943 Arthralgia of temporomandibular joint UMLS C2911645 Weight loss adverse event C0004114 Astrocytoma HSDN C0027796 Neuralgias C0006114 Cerebral edema HSDN C0018784 Deafness sensorineural C0432269 Lenz majewski hyperostotic dwarfism MalaCards|HPO C3274924 Have been coughing C0220981 Metabolic acidosis HSDN C4084775 Usual severity weight loss C0036974 Shock HSDN C0233576 Mannerism C0040953 Trichotillomania UMLS C0184567 Pain acute C0037051 Behavior illness HSDN C0231528 Muscle pain generalized C0302363 Bang disease MalaCards C0030486 Extremity paralysis, lower C0042514 Tachycardia, ventricular HSDN C0522224 Palsied C0016169 Pathologic fistula HSDN C1549543 Administration method - pain C1135957 Narrative HSDN C4084776 Weight loss C0003857 Congenital arteriovenous malformation HSDN C2127523 Left hand atrophy C0333641 Atrophic UMLS C0008031 Pain chest C0019829 Hodgkin disease OrphaNet C0851578 Disorder sleep C0034069 Pulmonary fibrosis HSDN C2108109 Continuous electrocardiogram sinus tachycardia C0406645 Amyopathic dermatomyositis MalaCards C1962956 Flatulence adverse event C0013394 Coitus painful HSDN C0013404 Respiratory difficulty C0155877 Allergic asthma DiseaseOntology C4084726 Distress cough C1540912 Hypereosinophilic syndrome HSDN C1963087 Constipation adverse event C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C0005745 Blepharoptosis C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C0085636 Light sensitivity C2751308 Cone dystrophy 4 (disorder) MalaCards|HPO|UMLS C2315100 Pediatric failure to thrive C0265316 Neurocutaneous syndromes MalaCards C0019079 Bloody sputum C0751878 Vasculitis, central nervous system HSDN C2984058 Have pain C0338480 Common migraine HSDN C1557397 Adverse event associated with pain C0014457 Eosinophilia HSDN C0030193 Sense of pain C0010633 Cystadenoma HSDN C3829611 Nausea frequency C1263846 Attention deficit hyperactivity disorder HSDN C4085222 Nausea C0022658 Kidney diseases HSDN C0007166 Cardiac output decreased C0037313 Sleep HSDN C0086565 Liver function abnormal C0272170 Shwachman syndrome HPO C1963249 Tinnitus adverse event C0038531 Subclavian artery stenosis HSDN C0010520 Skin cyanosis C0032965 Pregnancy complications, infectious HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027859 Acoustic neuroma HSDN C1963252 Tremor adverse event C0752125 Spinocerebellar ataxia type 7 MalaCards|HPO C0030554 Abnormal sensation C0032962 Pregnancy complications HSDN C1263846 Attention deficit disorder with hyperactivity C0079588 Ichthyosis, x-linked OrphaNet|HPO|MalaCards C0009806 Constipate C0022116 Ischemia HSDN C1963091 Diarrhea adverse event C0016053 Fibromyalgia HSDN C0700590 Diaphoresis excessive C0033922 Psychomotor disorders MalaCards C3829611 Nausea frequency C2675211 Episodic ataxia, type 6 (disorder) MalaCards C4084767 Bothered by vomiting C1864996 Enteric neuropathy, familial MalaCards C0030552 Paralysis partial C1857776 3-@methylglutaconic aciduria, type v MalaCards|HPO C1963281 Vomiting adverse event C0314657 Genetic predisposition HSDN C1961131 Cough adverse event C0003850 Arteriosclerosis HSDN C2984057 Have nausea C0007099 Carcinoma in situ HSDN C0036572 Convulsion C0032344 Poisoning aspects HSDN C2911645 Weight loss adverse event C0023885 Liver abscess HSDN C0042798 Vision dim C1849128 Spastic paraplegia 15, autosomal recessive MalaCards|HPO C0026205 Pupillary constriction C0009363 Congenital ocular coloboma (disorder) HSDN C1971624 Appetite absent C2984299 Asthma pathway HSDN C0004604 Pain back C0014457 Eosinophilia HSDN C1963087 Constipation adverse event C1845862 Creatine deficiency, x-linked OrphaNet|HPO|MalaCards C0426579 Anorexia symptom C0037661 Somatostatinoma OrphaNet|MalaCards C0007758 Cerebellar ataxia C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome MalaCards C3829611 Nausea frequency C0409959 Osteoarthritis, knee HSDN C3815497 Cough C0003949 Asbestosis HSDN C0850758 Pain pelvic C0041960 Ureterocele HSDN C1999266 Depression adverse event C0342859 Harderoporphyria HPO C3539020 Pelvic pain decreasing in frequency C1458155 Mammary neoplasms HSDN C0015799 Feminisation C0032578 Polyploidy HSDN C0015230 Exanthem C4076244 Eruption of skin co-occurrent with human immunodeficiency virus infection UMLS C2203646 Jaundice C2188545 Anuria HSDN C1963170 Hypothermia adverse event C0038525 Subarachnoid hemorrhage HSDN C4050613 Anxiety C2936741 Syndrome xxyy OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0039590 Testicular neoplasms HSDN C0086565 Liver function abnormal C0008350 Cholelithiasis MalaCards|HPO C4084776 Weight loss C0024692 Mandible fracture HSDN C0241165 Skin thickening C0271695 Rabson-mendenhall syndrome OrphaNet C0405089 Fatigue+pregnancy - not deliv. C2113881 Pregnancy-induced fatigue as antepartum condition UMLS C4049644 Depression C0041408 Turner syndrome MalaCards C0080233 Dental loss C3279792 Short-rib thoracic dysplasia 7 with or without polydactyly MalaCards C0749343 Thigh pain intermittent C0740728 Lower extremity problem UMLS C1963281 Vomiting adverse event C1963067 Atrial fibrillation adverse event HSDN C0017565 Gingiva hemorrhage C3463916 Complement factor i (c3 inactivator) deficiency MalaCards C4084726 Distress cough C0012546 Diphtheria HSDN C1069915 Vertigo C0004935 Animal ethology HSDN C0234146 Absent reflex C4015635 Charcot-marie-tooth disease, axonal, type 2t MalaCards C0015672 Decreased energy C1527258 Infantile paralysis MalaCards C0026838 Spasticity muscle C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO|UMLS C4085210 Usual severity pain C0015461 Facial neoplasms HSDN C0033377 Caudal displacement C3806742 Colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation MalaCards C0033774 Skin pruritus C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0038506 Stutter C0033944 Psychosexual development HSDN C0040264 Ear ringing sound C0043251 Wounds and injuries HSDN C0020578 Hyperventilate C0012746 Dissociative disorder HSDN C0518090 Frequency of pain question C0206721 Inverted papilloma HSDN C4084725 Usual severity cough C0017178 Gastrointestinal diseases HSDN C0034150 Skin purpura C0037999 Splenic neoplasms HSDN C0013404 Respiratory difficulty C0152108 Suberosis DiseaseOntology C0004134 Dyssynergia C0037274 Dermatologic disorders HSDN C0003862 Pain joint C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome OrphaNet|MalaCards C0812426 Kidney problem C0340608 Renal artery thrombosis UMLS C0426579 Anorexia symptom C0018799 Heart diseases HSDN C0000737 Abdomen pain C0085702 Monocytosis UMLS C0041667 Low weight C3698541 Ohdo syndrome, maat-kievit-brunner type MalaCards C1963093 Dizziness adverse event C0020476 Hyperlipoproteinemias HSDN C3463815 Feel fatigue C0027932 Neurotic disorders HSDN C0178417 Anhedonia C0003469 Anxiety disorders HSDN C0042963 Symptoms vomiting C1579931 Depressed - symptom HSDN C3463815 Feel fatigue C1847319 Paraganglioma and gastric stromal sarcoma MalaCards C0033774 Skin pruritus C0221056 Adult type dermatomyositis OrphaNet|HSDN|MalaCards C0009806 Constipate C1739094 Foodborne botulism OrphaNet|MalaCards C4084775 Usual severity weight loss C0149721 Left ventricular hypertrophy HSDN C4085210 Usual severity pain C0015414 Eye neoplasms HSDN C4084775 Usual severity weight loss C0033054 Prenatal exposure delayed effects HSDN C1962972 Proteinuria adverse event C2930815 Acute cerebral gaucher disease MalaCards C3203358 Alveolar hypoventilation C0027651 Tumor HSDN C2911647 Weight gain adverse event C0014118 Endocarditis HSDN C0036572 Convulsion C4015141 Mental retardation, autosomal dominant 29 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0017672 Pain tongue C0017689 Glucagonoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0021295 Infant, premature, diseases HSDN C4085222 Nausea C0015328 Behavior, exploratory HSDN C0033774 Skin pruritus C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards|UMLS C1963071 Back pain adverse event C0453996 Tobacco smoking HSDN C0518090 Frequency of pain question C0302280 Adrenogenital syndrome HSDN C0011991 Loose stools C0010823 Cytomegalovirus infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026683 Mucocele HSDN C4050613 Anxiety C1853445 Parkinson disease 7, autosomal recessive early-onset MalaCards|HPO C0023380 Lethargy C0268151 Classical galactosemia MalaCards|HPO C0241210 Speaking delay C3495551 Dihydropyrimidinuria MalaCards C2315100 Pediatric failure to thrive C0685894 Congenital absence of thymus MalaCards C0518090 Frequency of pain question C0854912 Pineal germinoma HSDN C0233514 Behavior abnormal C0238111 Lennox-gastaut syndrome OrphaNet|MalaCards C0030193 Sense of pain C0018552 Hamartoma HSDN C0015230 Exanthem C0582412 Bowenoid actinic keratosis UMLS C0018772 Deafness C0796068 Oculodigitoesophagoduodenal syndrome HPO C0022346 Yellow skin C0750426 Wbc elevated HSDN C0011175 Deficient fluid volume C1855849 Bartter syndrome, antenatal , type 2 HPO C1096082 Esophageal discomfort C0860534 Esophageal closed sensation of UMLS C2029884 Hearing loss by exam C0391889 Bony union HSDN C0036572 Convulsion C0205711 Pelizaeus-merzbacher disease OrphaNet|UMLS|HPO|MalaCards C4084802 Usual severity diarrhea C0035228 Respiratory hypersensitivity HSDN C0036572 Convulsion C0027707 Nephritis, interstitial HSDN C0013421 Dystonia C0268595 Glutaric aciduria, type 1 OrphaNet|HPO C0026205 Pupillary constriction C0439840 Reflex motion descriptor HSDN C0231341 Aging premature C0005944 Metabolic bone disorder HSDN C0234979 Dysdiadochokinesia C2750234 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 MalaCards|HPO|UMLS C0013421 Dystonia C0268250 Gaucher disease, type 2 (disorder) OrphaNet|HPO|MalaCards C0002965 Crescendo angina C0026764 Multiple myeloma HSDN C0150055 Pain chronic C0027627 Neoplasm metastasis HSDN C0030486 Extremity paralysis, lower C1704972 Genomic orientation HSDN C4084802 Usual severity diarrhea C0019243 Angioedemas, hereditary HPO C0040034 Thrombocytopenia C0585216 Alpha-thalassemia myelodysplasia syndrome OrphaNet|HPO C0242936 Center pain C0013589 Ectromelia HSDN C0013604 Edematous C0358297 Anthrax vaccines HSDN C2919142 Short stature adverse event C2931484 Cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation OrphaNet|MalaCards C4085642 Level of joint stiffness C1855310 Megaepiphyseal dwarfism MalaCards C0221263 Cafe au lait spot C1257915 Intestinal polyposis HSDN C0700590 Diaphoresis excessive C0023931 Lobstein's disease OrphaNet C0013595 Eczematous dermatitis C1721006 Keratoderma, palmoplantar, epidermolytic OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C1833699 Osteopoikilosis, isolated OrphaNet|HPO|MalaCards C0018772 Deafness C1861516 Cleidocranial dysplasia, forme fruste, with brachydactyly HPO C0009421 Comatose C0517555 Venous thrombosis after immobility HSDN C0241210 Speaking delay C2930926 Autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes MalaCards C0020578 Hyperventilate C0041296 Tuberculosis HSDN C0036396 Sciatica C0439840 Reflex motion descriptor HSDN C0010200 Cough symptom C0854989 Recurrent squamous cell carcinoma of lung UMLS C4084723 Constipation C0038160 Staphylococcal infections HSDN C0040460 Dental pain C0019693 Hiv infections HSDN C0019209 Large liver C0268307 Conjugated hyperbilirubinemia MalaCards C0151786 Weakness muscle C1833508 Carnitine palmitoyltransferase ii deficiency, late-onset OrphaNet|HPO C1963249 Tinnitus adverse event C0022658 Kidney diseases HSDN C1963071 Back pain adverse event C0018081 Gonorrhea HSDN C0518090 Frequency of pain question C0271650 Impaired glucose tolerance HSDN C3274924 Have been coughing C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C4085222 Nausea C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0234132 Pyramidal sign C1864663 Hypomyelination and congenital cataract OrphaNet|UMLS|HPO|MalaCards C0009792 Consciousness disorder C0035042 Psychology and religion HSDN C0242936 Center pain C0013363 Dysautonomia HSDN C0020305 Fetal edema C0542428 Hypochondrogenesis HPO C0020578 Hyperventilate C0013928 Fat embolism HSDN C0234376 Tremor action C3554518 Cowden syndrome 5 MalaCards C0018989 Paresis of one side of body C1856143 Hemolytic uremic syndrome, typical MalaCards C0018991 Paralysis one side of body C0006277 Bronchitis HSDN C0522224 Palsied C4050613 Anxiety scale (basc-2) HSDN C4084776 Weight loss C0008066 Child behavior disorders HSDN C3641756 Have diarrhea C0032343 Poisoning HSDN C0012569 Double vision C0014084 Enchondromatosis HSDN C2315100 Pediatric failure to thrive C2930971 Acroosteolysis dominant type MalaCards|HPO C0009421 Comatose C0220847 C hepatitis virus HSDN C4085210 Usual severity pain C3469186 Hemochromatosis, type 1 HSDN C2029884 Hearing loss by exam C0016788 Fucosidase deficiency disease MalaCards C1384666 Decreased hearing C0796202 Wittwer syndrome MalaCards C0019214 Hepatosplenomegaly C0043208 Wolman disease HPO C1443924 Severe diarrhea C0152945 Anthrax gastrointestinal MalaCards C0026205 Pupillary constriction C0023348 Leprosy, lepromatous HSDN C0243026 Generalized infection C1850407 Navajo familial neurogenic arthropathy MalaCards C3665347 Vision impaired C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C0234979 Dysdiadochokinesia C2931903 Menzel type olivopontocerebellar atrophy MalaCards C0393766 Postviral excessive daytime sleepiness C0042769 Virus diseases UMLS C0242936 Center pain C0234421 Conscious HSDN C3641756 Have diarrhea C0023176 Lead poisoning MalaCards|HSDN C0004134 Dyssynergia C0033817 Pseudomonas infections HSDN C4085661 Usual severity nausea C0013182 Drug allergy HSDN C4085661 Usual severity nausea C0021359 Infertility HSDN C0036572 Convulsion C0477371 Other forms of epilepsy nos UMLS C0413252 Hypothermia due to exposure C0019294 Hernia, inguinal HSDN C3494358 Characteristic, prodromal C1510539 Emotional intelligence HSDN C0010200 Cough symptom C0032965 Pregnancy complications, infectious HSDN C0042963 Symptoms vomiting C0021783 Internal external locus of control HSDN C2984057 Have nausea C0003864 Arthritis HSDN C4084767 Bothered by vomiting C0011269 Dementia, vascular HSDN C4084766 Vomiting C0206671 Eccrine acrospiroma HSDN C2911647 Weight gain adverse event C0027794 Neural tube defects HSDN C0018772 Deafness C0018552 Hamartoma HSDN C0038002 Spleen enlargement C0340834 Hennekam lymphangiectasia lymphedema syndrome MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C3203359 Rupture HSDN C4085548 Usual severity dizziness C0033860 Psoriasis HSDN C0018991 Paralysis one side of body C1550639 Specimen type - fistula HSDN C0031911 Pigment deposition C0152018 Esophageal carcinoma MalaCards C2315100 Pediatric failure to thrive C1853736 Congenital disorder of glycosylation, type iib OrphaNet|HPO|MalaCards C0040034 Thrombocytopenia C0854176 Malignant hepato-biliary neoplasm MalaCards C0557874 Global developmental delay C0393702 Myoclonic astatic epilepsy MalaCards|HPO C0043094 Weight gain C0600564 Self-efficacy HSDN C0030552 Paralysis partial C0268242 Niemann-pick disease, type a MalaCards|HSDN|HPO C2032396 Pelvic pain on the right C0009244 Behavioral cognitive therapy HSDN C0036572 Convulsion C0035921 Congenital rubella syndrome MalaCards C0004134 Dyssynergia C1704299 Hypobetalipoproteinemia, familial, apolipoprotein b MalaCards C1579931 Depressed - symptom C2930674 Babesioses, human MalaCards C1963170 Hypothermia adverse event C0032371 Poliomyelitis HSDN C0030552 Paralysis partial C0206366 Ossification of posterior longitudinal ligament HSDN C0028738 Nystagmus C3809356 Multiple congenital anomalies-hypotonia-seizures syndrome 3 MalaCards C0151786 Weakness muscle C0043255 Stab wound HSDN C0018772 Deafness C0334123 Histiocytosis, lipoid MalaCards C0026858 Musculoskeletal pain C1962963 Osteoporosis adverse event HSDN C3539896 Pelvic pain occurs with urination C0016548 Foreign body migration HSDN C0023380 Lethargy C0206093 Neuroectodermal tumors HSDN C0151889 Reflexes tendon increased C2751938 Cerebral palsy, spastic quadriplegic, 1 MalaCards|HPO C4084725 Usual severity cough C0038013 Ankylosing spondylitis HSDN C1963065 Apnea adverse event C0026896 Myasthenia gravis HSDN C4085661 Usual severity nausea C0001403 Addison disease HSDN C0011168 Disorder deglutition C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO C0332563 Papulae C0151436 Vasculitis, leukocytoclastic, cutaneous OrphaNet|MalaCards C0034933 Abnormal reflexes C0014550 Epilepsies, myoclonic HSDN C0009421 Comatose C0009938 Bruising HSDN C4084784 Diarrhea C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0557874 Global developmental delay C3553788 Alternating hemiplegia of childhood 2 MalaCards C4085211 Pain distress question C0023234 Legg-calve-perthes disease HSDN C2919142 Short stature adverse event C0086431 Hurler-scheie syndrome OrphaNet|HPO C0221263 Cafe au lait spot C0029405 Osteitis fibrosa cystica HSDN C0007758 Cerebellar ataxia C1855255 Pseudoarylsulfatase a deficiency MalaCards|HPO C0242936 Center pain C0033367 Projective techniques HSDN C0032285 Pneum C0342337 Insulin resistance syndrome, type b MalaCards C3641756 Have diarrhea C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards C0522224 Palsied C1963090 Dehydration adverse event HSDN C2024878 Cardiovascular surgery result: dyspnea C0007873 Uterine cervical neoplasm HSDN C4084784 Diarrhea C0030330 Panniculitis, peritoneal HSDN C0020578 Hyperventilate C3541306 Plasmodium measurement HSDN C4084726 Distress cough C0042111 Urticaria pigmentosa MalaCards C0022346 Yellow skin C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C0040485 Wryneck C0029423 Cartilaginous exostosis HSDN C0035078 Failure kidney C3665382 2,8-dihydroxyadenine urolithiasis OrphaNet|MalaCards C0020578 Hyperventilate C0243026 Sepsis HSDN C1963249 Tinnitus adverse event C0750929 Arnold-chiari malformation, type i MalaCards C1860844 Sparse, thin hair C0033300 Progeria OrphaNet|HPO C0413252 Hypothermia due to exposure C1962979 Burn adverse event HSDN C0037317 Sleep disturbance C0751666 Canavan disease, infantile OrphaNet|HPO C3641756 Have diarrhea C0001430 Adenoma HSDN C0231528 Muscle pain generalized C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO|UMLS C1963091 Diarrhea adverse event C0010631 Cystadenocarcinoma HSDN C0030193 Sense of pain C0015671 Father HSDN C0015469 Facial paralysis C0016398 Focal infection, dental HSDN C1963071 Back pain adverse event C0033953 Psychosexual disorders HSDN C0034150 Skin purpura C0021368 Inflammation HSDN C1963087 Constipation adverse event C0001403 Addison disease OrphaNet C0017181 Gastrointestinal bleed C3494187 Factor viii deficiency MalaCards C1963180 Neck pain adverse event C3244301 Coverage level - family HSDN C3815497 Cough C0021818 Intervertebral disk displacement HSDN C4084784 Diarrhea C0016169 Pathologic fistula HSDN C0151825 Ostalgia C0279584 B-cell childhood acute lymphoblastic leukemia UMLS C2984057 Have nausea C1963211 Pericarditis adverse event HSDN C0231218 Malaise generalized C2981627 Stage iva intrahepatic cholangiocarcinoma UMLS C0026838 Spasticity muscle C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0010200 Cough symptom C0019195 Hepatitis, viral, human HSDN C4084726 Distress cough C0020550 Hyperthyroidism HSDN C0018784 Deafness sensorineural C1836027 Deafness, autosomal recessive 23 MalaCards|HPO C3815497 Cough C0040136 Thyroid neoplasm HSDN C0030552 Paralysis partial C0007137 Squamous cell carcinoma HSDN C0037763 Spasm C0497327 Dementia HSDN C1557397 Adverse event associated with pain C0700359 Organophosphate poisoning HSDN C2984058 Have pain C0024131 Lupus vulgaris HSDN C2984058 Have pain C0016085 Filariasis HSDN C0013395 Indigestion C0018802 Congestive heart failure HSDN C1384666 Decreased hearing C0003090 Ankylosis HSDN C0004604 Pain back C0039231 Tachycardia HSDN C1963086 Confusion adverse event C0003467 Anxiety HSDN C4084726 Distress cough C0005592 Bird fancier's lung DiseaseOntology|MalaCards C0476273 Distress respiratory C2931296 Yorifuji okuno syndrome HPO C0349588 Stature short C0175699 Saethre-chotzen syndrome MalaCards|HPO C4084723 Constipation C0265246 Townes syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0036349 Paranoid schizophrenia HSDN C0003550 Broca aphasia C0010054 Coronary arteriosclerosis HSDN C0018524 Hallucinate C0085209 Bovine spongiform encephalitis MalaCards C0242936 Center pain C0033835 Pseudopseudohypoparathyroidism HSDN C0030193 Sense of pain C0042514 Tachycardia, ventricular HSDN C0241137 Skin pallor C0015499 Factor v deficiency HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0008370 Cholestasis HSDN C0028738 Nystagmus C1859570 Bardet-biedl syndrome 12 HPO C0040460 Dental pain C0016398 Focal infection, dental HSDN C0039070 Collapse fleeting C0021670 Insulinoma HSDN C0007758 Cerebellar ataxia C4225236 Spinocerebellar ataxia, autosomal recessive 21 UMLS C0557874 Global developmental delay C2674127 Loeys dietz syndrome, type 2a (disorder) MalaCards C0232943 Metromenorrhagia C0043397 Yellow fever, jungle MalaCards C0011570 Monopolar depression C2930798 Alexanders leukodystrophy MalaCards C0011206 Delirium acute C0037320 Night terrors HSDN C0026821 Cramp C0042830 Perception visual HSDN C4084768 Usual severity vomiting C0017668 Focal glomerulosclerosis HSDN C0026821 Cramp C0040034 Thrombocytopenia HSDN C0018520 Breath odor C0079487 Helicobacter infections HSDN C0149793 Transient monocular blindness C0751019 Carotid circulation transient ischemic attack UMLS C4084727 Cough frequency C0001261 Actinomycosis HSDN C0221232 Welts C0274440 Transfusion reaction, urticarial UMLS C0010520 Skin cyanosis C1963198 Pancreatitis adverse event HSDN C0878773 Bladder hyperactive C0036864 Sexual relations HSDN C4085317 Diarrhea frequency C0001815 Primary myelofibrosis HSDN C1963071 Back pain adverse event C0158683 Polycystic liver disease MalaCards|HPO C4085548 Usual severity dizziness C0021361 Female infertility HSDN C0018784 Deafness sensorineural C0037397 Behavior social HSDN C0013404 Respiratory difficulty C0236969 Substance-related disorders HSDN C0576456 Poor feeding C2931168 Hemangiomas, and cutaneous and intracranial vascular deformations MalaCards C0011991 Loose stools C0013080 Down syndrome HSDN|UMLS C1557397 Adverse event associated with pain C0026691 Mucocutaneous lymph node syndrome HSDN C3641756 Have diarrhea C0018944 Hematoma HSDN C4085211 Pain distress question C0006109 Brain damage, chronic HSDN C0032617 High urine output C0025202 Melanoma HSDN C1963091 Diarrhea adverse event C0035920 Rubella HSDN C0023012 Delay language C3809160 Shaheen syndrome MalaCards C1549543 Administration method - pain C1136154 Dysfunction, tibialis posterior HSDN C0005745 Blepharoptosis C0339085 Blepharochalasis, struma, double lip syndrome OrphaNet|MalaCards C0016199 Pain flank C3495801 Granulomatosis with polyangiitis HSDN C0522347 Ear pressure sensation C0948296 Discomfort ear UMLS C0413252 Hypothermia due to exposure C0006114 Cerebral edema HSDN C1557397 Adverse event associated with pain C1963088 Cystitis adverse event HSDN C0003862 Pain joint C0001430 Adenoma HSDN C0242936 Center pain C0042164 Uveitis HSDN C1963091 Diarrhea adverse event C0027858 Neuroma HSDN C0015469 Facial paralysis C0021841 Intestinal neoplasms HSDN C0242936 Center pain C0011875 Diabetic angiopathies HSDN C4084802 Usual severity diarrhea C0001206 Acromegaly HSDN C0039070 Collapse fleeting C0011265 Presenile dementia HSDN C0013395 Indigestion C0019284 Diaphragmatic hernia HSDN C2315100 Pediatric failure to thrive C0398691 Hyperimmunoglobulinemia d MalaCards C0042963 Symptoms vomiting C0162531 Hereditary coproporphyria HSDN|HPO C0344232 Blurred vision C0342898 Apolipoprotein a-i deficiency OrphaNet|HPO C0034933 Abnormal reflexes C0007771 Intracranial arteriosclerosis HSDN C0015672 Decreased energy C1709578 Pleural sarcomatoid mesothelioma UMLS C0033774 Skin pruritus C0024299 Lymphoma HSDN C0017181 Gastrointestinal bleed C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C1963086 Confusion adverse event C0011581 Depressive disorder HSDN C1963091 Diarrhea adverse event C0342257 Complications of diabetes mellitus HSDN C0039231 Heartbeats increased C0007279 Carotid body paraganglioma HPO C0022346 Yellow skin C0024305 Lymphoma, non-hodgkin HSDN C0030552 Paralysis partial C0027095 Myosarcoma HSDN C0037317 Sleep disturbance C1835614 Hereditary hyperexplexia MalaCards C3641756 Have diarrhea C0585274 Periodic syndrome OrphaNet|HPO C1856661 Cornea cloudy C2931795 Chromosome 11, deletion 11p OrphaNet C0917816 Deficiency mental C2930820 Incontinentia pigmenti, familial male lethal type MalaCards|HPO C0019209 Large liver C2673635 Combined saposin deficiency MalaCards|HPO C2203646 Jaundice C0238339 Hereditary pancreatitis MalaCards|HSDN|HPO C3163620 Hypotension adverse event C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0002170 Alopecia disorders C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C1963091 Diarrhea adverse event C0021364 Male infertility HSDN C3829611 Nausea frequency C0002736 Amyotrophic lateral sclerosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040137 Thyroid nodule HSDN C0012569 Double vision C0033578 Prostatic neoplasms HSDN C4085210 Usual severity pain C0206698 Cholangiocarcinoma HSDN C2919142 Short stature adverse event C2919796 Glycogen storage disease type ia OrphaNet|MalaCards C0020578 Hyperventilate C0006107 Concussion HSDN C0424755 Fever symptoms C0006309 Brucellosis DiseaseOntology|MalaCards C1963137 Hydrocephalus adverse event C2931058 Marfan syndrome type 2 MalaCards C1838869 Proximal neurogenic muscle weakness C0393807 Hereditary motor and sensory neuropathy with optic atrophy (disorder) HPO C4084727 Cough frequency C0005686 Urinary bladder diseases HSDN C4084784 Diarrhea C0239981 Hypoalbuminemia HSDN C0518090 Frequency of pain question C0006849 Oral candidiasis HSDN C4084767 Bothered by vomiting C0151620 Hypertensive encephalopathy HSDN C4084725 Usual severity cough C0040128 Thyroid diseases HSDN C1279888 Proteinuria of undiagnosed cause C0018051 Gonadal dysgenesis HSDN C4085317 Diarrhea frequency C0012739 Disseminated intravascular coagulation HSDN C0036572 Convulsion C0018915 Hemangioendothelioma HSDN C4084802 Usual severity diarrhea C0026896 Myasthenia gravis HSDN C1962956 Flatulence adverse event C0019693 Hiv infections HSDN C0242936 Center pain C0338437 Neurocysticercosis HSDN C1384666 Decreased hearing C2931912 Mende syndrome MalaCards C1557397 Adverse event associated with pain C0752308 Hypoxia-ischemia, brain HSDN C0011991 Loose stools C0014474 Ependymoma HSDN C4085549 Dizziness C0034088 Pulmonary valve insufficiency HSDN C1069915 Vertigo C1556682 Adverse event associated with infection HSDN C0497247 Blood pressure elevation C0040028 Thrombocythemia, essential HPO C0013404 Respiratory difficulty C0030442 Progressive bulbar palsy HSDN C4085210 Usual severity pain C0008370 Cholestasis HSDN C0004604 Pain back C0034929 Reflex HSDN C3815497 Cough C0023786 Mucopolysaccharidosis i OrphaNet C0151798 Liver necrosis C0220620 Gastrointestinal carcinoid tumor MalaCards C0426579 Anorexia symptom C0206624 Hepatoblastoma MalaCards C0085636 Light sensitivity C2931411 Flotch syndrome OrphaNet|MalaCards C0036572 Convulsion C0029001 Onchocerciasis HSDN C0010200 Cough symptom C1708769 Lung clear cell adenocarcinoma UMLS C0150045 Urinary incontinence urge C0001418 Adenocarcinoma HSDN C4085222 Nausea C1720777 Functional laterality HSDN C0020458 Hyperhydrosis C0040156 Thyrotoxicosis MalaCards C3463815 Feel fatigue C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0031256 Petechia C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C3539020 Pelvic pain decreasing in frequency C0037274 Dermatologic disorders HSDN C2203646 Jaundice C0013289 Duodenal diseases HSDN C0013421 Dystonia C0338488 Alternating hemiplegia of childhood HPO C4084784 Diarrhea C0002453 Amenorrhea HSDN C2911647 Weight gain adverse event C1553188 Hemolysis - observation HSDN C0518090 Frequency of pain question C0037859 Spermatocele HSDN C0012833 Dizzy C1579931 Depressed - symptom HSDN C4084921 Usual severity itching C0153246 Tinea manus DiseaseOntology|MalaCards C0009421 Comatose C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C3887873 Hearing loss C3494419 Deformities, dentofacial HSDN C4084774 Have weight loss C0232488 Abdominal colic HSDN C0150045 Urinary incontinence urge C0041974 Urethral stricture HSDN C0004941 Behavioral symptoms C0393576 Chorea acanthocytosis syndrome OrphaNet C0011991 Loose stools C0005779 Blood coagulation disorders HSDN C4084897 Sleep disturbance subordinate domain C0795833 Kleefstra syndrome HPO C0042571 Vertigo subjective C2586211 Thrombosis of blood vessel HSDN C3641756 Have diarrhea C0017150 Gastrinoma OrphaNet|MalaCards C0557874 Global developmental delay C3809483 Sli5 MalaCards C3815497 Cough C0012691 Dislocations HSDN C1963184 Nystagmus adverse event C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0009792 Consciousness disorder C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0151786 Weakness muscle C3850024 Transcranial direct current stimulation HSDN C0020455 Hypergammaglobulinemia C0027051 Myocardial infarction HSDN C1279888 Proteinuria of undiagnosed cause C0011168 Deglutition disorders HSDN C4084725 Usual severity cough C0006277 Bronchitis MalaCards C0035078 Failure kidney C0162510 Caroli disease HPO C0085631 Abnormal excitement C0036349 Paranoid schizophrenia HSDN C0026603 Motion sickness C0033941 Psychoses, substance-induced HSDN C0030552 Paralysis partial C0033968 Psychotherapeutic technique HSDN C0026858 Musculoskeletal pain C0007097 Carcinomas HSDN C0151786 Weakness muscle C0410174 Fukuyama type congenital muscular dystrophy MalaCards|HPO C3146279 Coma C0205710 Alpers syndrome (disorder) OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C0018777 Deafness, conductive C1855433 Mandibulofacial dysostosis, treacher collins type, autosomal recessive MalaCards C0157725 Other spec pruritic conditions C0810052 Other inflammatory condition of skin UMLS C3898969 Have been vomiting C0023817 Hyperlipoproteinemia type i HPO C0011991 Loose stools C0015423 Eyelid diseases HSDN C0460137 Push down or depress C1864851 Pigmented nodular adrenocortical disease, primary, 2 HPO C1549543 Administration method - pain C0015630 Fantasies HSDN C4049644 Depression C3149705 Parkinson disease 1, autosomal dominant lewy body HPO C0241426 Tongue burning sensation C0406669 Psychogenic sensory disturbance of skin UMLS C0011991 Loose stools C0025472 Mesenteric vascular occlusion HSDN C3539892 Pelvic pain in front C0269185 Uterus retroverted HSDN C4085210 Usual severity pain C0020598 Hypocalcemia HSDN C0235046 Paresthesia skin C0030554 Paresthesia UMLS C0332566 Maculopapule C0275755 Achromic and hyperchromic skin lesions of carate UMLS C1963063 Anorexia adverse event C0460137 Push down or depress HSDN C0151686 Growth retardation C0079474 Hallopeau-siemens disease HPO C0030193 Sense of pain C0002886 Anemia, macrocytic HSDN C0917816 Deficiency mental C3810326 Spinocerebellar ataxia, autosomal recessive 15 MalaCards C0860603 Anxiety symptom C1855606 Burton syndrome MalaCards C1962956 Flatulence adverse event C0013369 Dysentery HSDN C2127372 Redness under lateral aspect of right upper eyelid C1862177 Diaphyseal medullary stenosis with malignant fibrous histiocytoma MalaCards C1963091 Diarrhea adverse event C0009326 Collagen diseases HSDN C0518090 Frequency of pain question C0032578 Polyploidy HSDN C0917816 Deficiency mental C1970848 Phosphoglycerate kinase 1 deficiency MalaCards|HPO C3178766 Nociceptive pain C0004361 Autogenic therapy HSDN C3641755 Have constipation C0036690 Septicemia HSDN C0237849 Skin desquamation C2749659 Aicardi-goutieres syndrome 5 (disorder) MalaCards C3641756 Have diarrhea C0008533 Hemophilia b HSDN C4084802 Usual severity diarrhea C0949272 Iieocolitis MalaCards C3274924 Have been coughing C0011127 Pressure ulcer HSDN C3463815 Feel fatigue C0021843 Intestinal obstruction HSDN C0020305 Fetal edema C0034902 Pure red-cell aplasia HSDN C0151603 Edema generalized C0023903 Liver neoplasms MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0019284 Diaphragmatic hernia HSDN C0085636 Light sensitivity C0948264 Neuroborreliosis MalaCards C0027066 Myoclonic jerking C4225289 Epilepsy, progressive myoclonic, 9 UMLS C4084724 Usual severity constipation C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C1963252 Tremor adverse event C0022701 Kinesthesia HSDN C0004134 Dyssynergia C1849088 Spinocerebellar ataxia with dysmorphism UMLS C0030193 Sense of pain C0025286 Meningioma HSDN C2911645 Weight loss adverse event C0030499 Parasitic diseases HSDN C4084727 Cough frequency C0038454 Cerebrovascular accident HSDN C1145670 Failure respiratory C0598226 Harlequin type ichthyosis HPO C0238656 Pain ankle C0018099 Gout UMLS C0020649 Blood pressure decreased C2678367 Renal tubular dysgenesis with choanal atresia and athelia HPO C0019825 Voice hoarseness C1336215 Stage iiia small cell carcinoma of lung UMLS C0019079 Bloody sputum C0242184 Hypoxia UMLS C0013395 Indigestion C0022660 Kidney failure, acute HSDN C0018834 Brash C0175691 Dubowitz syndrome MalaCards C2984058 Have pain C0026918 Mycobacterium infections HSDN C3829611 Nausea frequency C1963211 Pericarditis adverse event HSDN C0522224 Palsied C0001080 Achondroplasia HSDN C0018772 Deafness C0015423 Eyelid diseases HSDN C0454644 Delayed language development C3495554 Homocarnosinase deficiency MalaCards C0004941 Behavioral symptoms C0026705 Mucopolysaccharidosis ii OrphaNet C1384666 Decreased hearing C3539923 Cdisc adas-cog - orientation summary score HSDN C3539023 Pelvic pain increasing in frequency C0006118 Brain neoplasms HSDN C4084784 Diarrhea C0021843 Intestinal obstruction HSDN C0037763 Spasm C0027531 Neck injury HSDN C0013595 Eczematous dermatitis C2678439 Cranioosteoarthropathy HPO C0031911 Pigment deposition C3645711 Congenital osteopetrosis MalaCards C0013395 Indigestion C0524910 Hepatitis c, chronic HSDN C0020796 Profoundly mentally retarded C4012727 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 MalaCards C1069915 Vertigo C1546533 Specimen source codes - abscess HSDN C0030552 Paralysis partial C1852456 Cryoglobulinemia, familial mixed OrphaNet|MalaCards C1962972 Proteinuria adverse event C3495422 Finding relating to sexuality and sexual activity HSDN C0232493 Epigastric pain C0206624 Hepatoblastoma MalaCards C0007859 Pain neck C0019693 Hiv infections HSDN C0011991 Loose stools C0011882 Diabetic neuropathies HSDN C0013595 Eczematous dermatitis C1846545 Autoimmune lymphoproliferative syndrome type 2b HPO C0013395 Indigestion C0024117 Chronic obstructive airway disease HSDN C0030193 Sense of pain C0028768 Obsessive-compulsive disorder HSDN C0030193 Sense of pain C0033941 Psychoses, substance-induced HSDN C3146279 Coma C0008149 Chlamydia infections HSDN C4085862 Bothered by nausea C0020544 Renal hypertension HSDN C0497247 Blood pressure elevation C0002066 Alkaptonuria MalaCards|HPO C0557874 Global developmental delay C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C4084774 Have weight loss C0034531 Experimental radiation injuries HSDN C0015300 Ocular proptosis C2674705 Osteolysis, hereditary, of carpal bones with or without nephropathy OrphaNet|HPO|MalaCards C0015469 Facial paralysis C0270932 Neuropathy paraneoplastic HSDN C4084726 Distress cough C2911643 Encounter due to family history of osteoporosis HSDN C0026826 High muscle tone C3554607 Mitochondrial complex iii deficiency, nuclear type 4 MalaCards C0155066 Visual loss, one eye, unqualif C1263864 Blindness and/or vision impairment level UMLS C0424755 Fever symptoms C0024299 Lymphoma HSDN C0036572 Convulsion C1852372 Mitochondrial complex iii deficiency (disorder) HPO C2024893 Cardiovascular surgery result: fatigue C0043194 Wiskott-aldrich syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0019357 Keratitis, herpetic HSDN C1963091 Diarrhea adverse event C0008049 Chicken pox HSDN C1963091 Diarrhea adverse event C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0020458 Hyperhydrosis C1851479 Keratoderma palmoplantaris transgrediens OrphaNet C0013595 Eczematous dermatitis C0795841 Jacobsen distal 11q deletion syndrome MalaCards|HPO C0003467 Angst C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084725 Usual severity cough C0520757 Delayed emergence from anesthesia HSDN C0034124 Pupillary disorder C0036161 Sandhoff disease HSDN C0013395 Indigestion C0038354 Stomach diseases UMLS C0040822 D tremors C0393590 Fahr's syndrome (disorder) MalaCards|HPO|UMLS C0033377 Caudal displacement C0393591 Aicardi-goutieres syndrome MalaCards|HPO C4085548 Usual severity dizziness C0010709 Cyst HSDN C3665347 Vision impaired C3151061 Retinitis pigmentosa 47 MalaCards|HPO C0002962 Angina C3489393 Hiatal hernia HSDN C1579931 Depressed - symptom C0751435 Hyperphenylalaninaemia MalaCards C0240715 Perineal lump C0156397 Vulval hematoma UMLS C0013362 Dysarthrias C0085541 Epilepsy, frontal lobe HSDN C1557397 Adverse event associated with pain C0042133 Uterine fibroids HSDN C4085210 Usual severity pain C0036918 Sexually transmitted diseases, viral HSDN C0020578 Hyperventilate C0007350 Cat disease HSDN C2984057 Have nausea C0020649 Hypotension HSDN C4084766 Vomiting C0022602 Actinic keratosis HSDN C2911645 Weight loss adverse event C0279626 Squamous cell carcinoma of esophagus MalaCards C4084769 Vomiting frequency C0021361 Female infertility HSDN C0039070 Collapse fleeting C0751815 Carotid artery, internal, dissection HSDN C0522224 Palsied C0812393 Cancer patients and suicide and depression HSDN C1963063 Anorexia adverse event C4084909 Depression subordinate domain HSDN C0002962 Angina C0011334 Dental caries HSDN C1557397 Adverse event associated with pain C0029422 Osteochondrodysplasias HSDN C1999266 Depression adverse event C2931673 Ceroid lipofuscinosis, neuronal 1, infantile MalaCards|HPO C0011206 Delirium acute C0015806 Femur neck fracture HSDN C0242936 Center pain C0010073 Coronary artery vasospasm HSDN C4084727 Cough frequency C0027627 Neoplasm metastasis HSDN C1963077 Bone pain adverse event C1367554 Adamantinoma OrphaNet|MalaCards C0349588 Stature short C0036069 Saldino-noonan syndrome MalaCards C0242936 Center pain C0022366 Jaw, edentulous HSDN C0700200 Presyncope C0007222 Cardiovascular diseases UMLS C4084727 Cough frequency C0007138 Carcinoma, transitional cell HSDN C2203646 Jaundice C1090821 Sepsis (invertebrate) HSDN C0041657 Consciousness loss C3163620 Hypotension adverse event HSDN C0003862 Pain joint C2873856 Essential cryoglobulinemia MalaCards C1557397 Adverse event associated with pain C0002878 Anemia, hemolytic HSDN C1069915 Vertigo C0023343 Leprosy HSDN C0557874 Global developmental delay C0271742 Glucocorticoid deficiency with achalasia HPO C1963184 Nystagmus adverse event C1839264 Spastic paraplegia 2, x-linked (disorder) MalaCards|HPO C0020455 Hypergammaglobulinemia C0152025 Polyneuropathy HSDN C1963063 Anorexia adverse event C1556682 Adverse event associated with infection HSDN C0028961 Urine output decreased C1999266 Depression adverse event HSDN C0857305 Thrombocytopenia purpura C0013295 Duodenal ulcer HSDN C0242936 Center pain C0242422 Parkinsonian disorders HSDN C1549543 Administration method - pain C0009763 Conjunctivitis HSDN C0020305 Fetal edema C0036069 Saldino-noonan syndrome MalaCards C3641756 Have diarrhea C0023676 Life style HSDN C4085317 Diarrhea frequency C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0013362 Dysarthrias C1843366 Niemann-pick disease, type c2 MalaCards|HPO C1963091 Diarrhea adverse event C0268525 5-oxoprolinase deficiency MalaCards|HPO C0020672 Body temperature decreased C0027627 Neoplasm metastasis HSDN C0013390 Cramps menstrual C0453996 Tobacco smoking HSDN C0018772 Deafness C0268425 Alstrom syndrome HSDN C3898969 Have been vomiting C3888018 Congenital hyperinsulinism MalaCards C0020578 Hyperventilate C0036690 Septicemia HSDN C4084784 Diarrhea C0043398 Yellow fever, urban MalaCards C0010200 Cough symptom C1837218 Cleft palate, isolated HSDN C2911645 Weight loss adverse event C0014859 Esophageal neoplasms OrphaNet|HSDN|MalaCards C0424755 Fever symptoms C0439840 Reflex motion descriptor HSDN C0040264 Ear ringing sound C0015302 External exotoses HSDN C0035229 Respiratory function impaired C0085435 Arthritis, reactive MalaCards C0004134 Dyssynergia C0268680 Biotin deficiency MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0085207 Gestational diabetes HSDN C4084802 Usual severity diarrhea C0026771 Trauma multiple HSDN C0030193 Sense of pain C0012739 Disseminated intravascular coagulation HSDN C0000737 Abdomen pain C0027831 Neurofibromatosis 1 HSDN C3887638 Failure to thrive in infant C1859536 Bare lymphocyte syndrome, type ii, complementation group c HPO C0012833 Dizzy C0005424 Biliary tract diseases HSDN C0022346 Yellow skin C3899982 Bclc stage 0 hepatocellular carcinoma UMLS C0019079 Bloody sputum C1708788 Lung typical carcinoid tumor UMLS C0020673 Hypothermia (central) (local) C0003838 Arterial occlusive diseases HSDN C0023380 Lethargy C0009952 Febrile convulsions HSDN C2911647 Weight gain adverse event C0085159 Seasonal affective disorder HSDN C1963177 Muscle pain adverse event C0268238 Triglyceride storage disease with ichthyosis MalaCards C0027497 Queasy C0151744 Myocardial ischemia HSDN C0018681 Headache, cephalalgia C0002949 Aneurysm, dissecting HSDN C0009806 Constipate C0265246 Townes syndrome OrphaNet|HPO|MalaCards C1962972 Proteinuria adverse event C1851347 Familial mediterranean fever, autosomal dominant HPO C1971624 Appetite absent C1552962 Units of measure - pica HSDN C0860603 Anxiety symptom C0268322 Chester-type porphyria HPO C0018784 Deafness sensorineural C3807295 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant MalaCards C0577567 Mass of urogenital structure C0017416 Genital neoplasms, female UMLS C0037036 Increased salivation C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards C1963064 Anxiety adverse event C0027873 Neuromyelitis optica MalaCards C0015672 Decreased energy C0017563 Gingival diseases HSDN C0460137 Push down or depress C1846707 Spinocerebellar ataxia 17 MalaCards|HPO C0015230 Exanthem C1444838 Chronic arthritis of juvenile onset OrphaNet C0043094 Weight gain C0020179 Huntington disease HSDN C0242936 Center pain C0263843 Band iliotibial syndromes HSDN C0020672 Body temperature decreased C2940786 Thyroid hormone resistance syndrome HPO C0002962 Angina C0011882 Diabetic neuropathies HSDN C0027497 Queasy C0036357 Psychology, schizophrenic HSDN C0024031 Back pain lower back C1556682 Adverse event associated with infection HSDN C0018926 Emesis bloody C1258215 Ileus HSDN C0085128 Cardiac output elevated C0037579 Soft tissue neoplasms HSDN C0036572 Convulsion C3494990 Myoclonic seizure, non-intractable UMLS C1963252 Tremor adverse event C0021295 Infant, premature, diseases HSDN C0587242 Pain due to knee joint prosth C1997440 Arthropathy of knee joint UMLS C3815497 Cough C0152937 Primary pneumonic plague DiseaseOntology|MalaCards C0016382 Cutaneous vascular engorgement C0263637 Angioma serpiginosum, x-linked MalaCards C0041657 Consciousness loss C0013928 Fat embolism HSDN C0011206 Delirium acute C0030567 Parkinson disease HSDN C0036659 Sensation disorder C1962986 Glaucoma adverse event HSDN C0005745 Blepharoptosis C2931394 Katsantoni papadakou lagoyanni syndrome OrphaNet|MalaCards C0020450 Hyperemesis gravidarum C0013418 Abnormal labor HSDN C0013362 Dysarthrias C0796205 Spinocerebellar ataxia, x-linked 1 MalaCards C0032617 High urine output C2749685 Cystinosis, atypical nephropathic (disorder) HPO C3274924 Have been coughing C0002994 Angioedema HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0520720 Cyst nerve root HSDN C4042891 Sleep wake disorders C0024141 Lupus erythematosus, systemic HSDN C0030552 Paralysis partial C0020659 Hypothalamic neoplasms HSDN C1962972 Proteinuria adverse event C0037930 Spinal cord neoplasms HSDN C0003811 Cardiac rhythm disturbance C2931029 Nevi flammei, familial multiple HPO C4084774 Have weight loss C1720189 Episodic ataxia MalaCards C0424755 Fever symptoms C0272258 Cryoglobulinemia, primary MalaCards C0020673 Hypothermia (central) (local) C0026850 Muscular dystrophy HSDN C4085211 Pain distress question C1552527 Clinic / center - developmental disabilities HSDN C0042963 Symptoms vomiting C0011175 Dehydration UMLS C2984057 Have nausea C0275148 Poisoning of animal by plant HSDN C0151889 Reflexes tendon increased C1706192 Sulfatidosis MalaCards C2242996 Tingling C0004935 Animal ethology HSDN C4084726 Distress cough C0006118 Brain neoplasms HSDN C3827868 Tachycardia by ecg finding C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C0042798 Vision dim C1850053 Pelizaeus-merzbacher-like disease, autosomal recessive, 2 MalaCards|HPO C0028738 Nystagmus C0079504 Hermanski-pudlak syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C1846058 Lubs x-linked mental retardation syndrome HPO|UMLS C0018808 Murmur C0039231 Tachycardia HSDN C0018775 Hearing loss bilateral C0276226 Herpes encephalitis HSDN C0233514 Behavior abnormal C1527231 Adrenomyeloneuropathy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3249881 Infection - suppurative HSDN C4084762 Usual severity shortness of breath C0155877 Allergic asthma DiseaseOntology C4084774 Have weight loss C1550639 Specimen type - fistula HSDN C1963170 Hypothermia adverse event C0018674 Head trauma HSDN C0026821 Cramp C0032371 Poliomyelitis HSDN C0002965 Crescendo angina C0010340 Critical illness HSDN C0013404 Respiratory difficulty C0009404 Colorectal neoplasms HSDN C0005779 Clotting C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0030486 Extremity paralysis, lower C0001807 Aggressive behavior HSDN C1963281 Vomiting adverse event C0042470 Guanarito haemorrhagic fever MalaCards C4084788 Have dizziness C0026650 Movement disorders HSDN C1963093 Dizziness adverse event C0034530 Injury radiation HSDN C4084784 Diarrhea C1837028 Severe combined immunodeficiency, autosomal recessive, t cell negative, b cell positive, nk cell positive HPO C0036572 Convulsion C1000587 Pemphigus HSDN C0242936 Center pain C0020564 Hypertrophy HSDN C2315100 Pediatric failure to thrive C1861923 Acampomelic campomelic dysplasia MalaCards|HPO C0034124 Pupillary disorder C0039223 Tabes dorsalis HSDN C4085211 Pain distress question C0038940 Surgical wound dehiscence HSDN C0557874 Global developmental delay C1865596 Desmosterolosis MalaCards|HPO C2911647 Weight gain adverse event C0037579 Soft tissue neoplasms HSDN C4084725 Usual severity cough C0021845 Intestinal perforation HSDN C4084727 Cough frequency C0238378 Desquamative interstitial pneumonia MalaCards C0242936 Center pain C0005818 Blood platelet disorders HSDN C1384666 Decreased hearing C1300257 Thanatophoric dysplasia, type 2 OrphaNet|HPO|MalaCards C0030193 Sense of pain C3244301 Coverage level - family HSDN C4085862 Bothered by nausea C0031039 Effusion pericardial HSDN C0018681 Headache, cephalalgia C0334590 Anaplastic oligodendroglioma UMLS C0349588 Stature short C1841696 Macdermot patton williams syndrome MalaCards C2108113 Continuous electrocardiogram ventricular tachycardia C1832680 Cardiomyopathy, dilated, 1e MalaCards C0042798 Vision dim C2677099 Crouzon syndrome with acanthosis nigricans (disorder) MalaCards|HPO C0041667 Low weight C1849157 Insulin-like growth factor i, resistance to MalaCards|HPO C0578055 Pain of head and neck region C0007863 Occipital neuralgia UMLS C4084767 Bothered by vomiting C0021845 Intestinal perforation HSDN C0013604 Edematous C0037286 Skin neoplasms HSDN C0015732 Feces incontinence C1527231 Adrenomyeloneuropathy MalaCards|HPO C0015469 Facial paralysis C1850671 Myosclerosis, autosomal recessive HPO C0009421 Comatose C0009375 Colonic neoplasms HSDN C0004134 Dyssynergia C0007820 Cerebrovascular disorders HSDN C0036572 Convulsion C0280483 Adult anaplastic astrocytoma UMLS C0011991 Loose stools C0000786 Spontaneous abortion HSDN C4085862 Bothered by nausea C0024266 Lymphocytic choriomeningitis DiseaseOntology|MalaCards C0023012 Delay language C3810406 Mental retardation, autosomal dominant 23 MalaCards C0521766 Nystagmus inhibited when fixation removed C0028738 Nystagmus UMLS C0030486 Extremity paralysis, lower C0039006 Swine--diseases HSDN C0231592 Joint crepitance C2015802 Other orthopedic disorders UMLS C1963154 Renal failure adverse event C1857423 Cystic kidney disease with ventriculomegaly MalaCards C1557397 Adverse event associated with pain C0020875 Ileal diseases HSDN C0878773 Bladder hyperactive C0001430 Adenoma HSDN C0011206 Delirium acute C0025202 Melanoma HSDN C3541349 Syncope C0018814 Heart rupture, post-infarction HSDN C0009421 Comatose C0022665 Kidney neoplasm HSDN C0000737 Abdomen pain C0005398 Cholestasis, extrahepatic HSDN C0000737 Abdomen pain C1709869 Rectosigmoid signet ring cell carcinoma UMLS C3163620 Hypotension adverse event C0266313 Allanson pantzar mcleod syndrome MalaCards|HPO C0039070 Collapse fleeting C1261473 Sarcoma HSDN C0037763 Spasm C0007222 Cardiovascular diseases HSDN C0031911 Pigment deposition C1266158 Nonseminomatous germ cell tumor MalaCards C4084768 Usual severity vomiting C4084909 Depression subordinate domain HSDN C0557874 Global developmental delay C1291386 D-glycericacidemia MalaCards|HPO C0206146 Myocardial stunning C0314657 Genetic predisposition HSDN C3808046 Breathing dysregulation C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C2237041 Shox gene with short stature C0265328 Alopecia-epilepsy-oligophrenia syndrome OrphaNet|MalaCards C2029884 Hearing loss by exam C0023702 Injury lightning HSDN C0042571 Vertigo subjective C3151295 Hypomagnesemia 6, renal MalaCards|HPO|UMLS C0234132 Pyramidal sign C2931646 Oculocerebral hypopigmentation syndrome type preus MalaCards C0042571 Vertigo subjective C0338487 Benign paroxysmal vertigo of childhood UMLS C0027066 Myoclonic jerking C0020457 Diabetic nonketotic hyperosmolar coma HSDN C0042798 Vision dim C2931008 Congenital disorder of glycosylation type 2a MalaCards C1999266 Depression adverse event C1956390 Cranial arteritis MalaCards C1557397 Adverse event associated with pain C0009480 Community psychiatry HSDN C0013604 Edematous C0040947 Trichostrongyloidiasis HSDN C0332563 Papulae C0398621 Hypoplasminogenemia MalaCards C0851578 Disorder sleep C1963274 Vasculitis adverse event HSDN C1557397 Adverse event associated with pain C0338437 Neurocysticercosis HSDN C1963249 Tinnitus adverse event C0035302 Retinal artery occlusion HSDN C2984058 Have pain C0034063 Pulmonary edema HSDN C0518090 Frequency of pain question C0085083 Ovarian hyperstimulation syndrome HSDN C0019079 Bloody sputum C1336124 Stage ia small cell carcinoma of lung UMLS C0427068 Legs weakness C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C1856661 Cornea cloudy C1845050 Pigmentary disorder, reticulate, with systemic manifestations HPO C0413252 Hypothermia due to exposure C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0424755 Fever symptoms C0011616 Contact dermatitis HSDN C0040822 D tremors C0344423 Atrial flutter by ecg finding HSDN C0030193 Sense of pain C0017400 Behavioral genetics HSDN C1963071 Back pain adverse event C0030354 Papilloma HSDN C1963252 Tremor adverse event C0700095 Central neuroblastoma HSDN C0848203 Male pelvic pain C0018965 Hematuria HSDN C4084727 Cough frequency C3887662 Intraspinal neoplasm HSDN C0038990 Sweats C1835650 Focal palmoplantar and gingival hyperkeratosis syndrome OrphaNet|MalaCards C4084774 Have weight loss C0015773 Felty syndrome OrphaNet|MalaCards C1145670 Failure respiratory C1842691 Diaphanospondylodysostosis MalaCards|HPO C0086565 Liver function abnormal C3887654 Polyarteritis nodosa, childhood-onset MalaCards C0018772 Deafness C0006105 Brain abscess HSDN C0085636 Light sensitivity C3808786 Albinism, oculocutaneous, type vii MalaCards C3463815 Feel fatigue C2706915 Language:-:point in time:^patient:- HSDN C0018681 Headache, cephalalgia C0343771 Human ehrlichiosis MalaCards C0017565 Gingiva hemorrhage C2700425 Ehlers-danlos syndrome, dermatosparaxis type HPO C0036572 Convulsion C0006845 Candidiasis, chronic mucocutaneous MalaCards|HPO C0030554 Abnormal sensation C2984299 Asthma pathway HSDN C0026821 Cramp C0010823 Cytomegalovirus infections HSDN C0423707 Lateral femoral cutaneous neuralgia C1290878 Disease of thigh UMLS C0010200 Cough symptom C0007137 Squamous cell carcinoma HSDN C1557397 Adverse event associated with pain C0042514 Tachycardia, ventricular HSDN C0004604 Pain back C0522255 Cervical root pain UMLS C0018524 Hallucinate C0036344 Schizophrenia, catatonic HSDN C0023380 Lethargy C0029944 Drug overdose HSDN C0020672 Body temperature decreased C0026769 Multiple sclerosis HSDN C0040822 D tremors C1847640 Kufor-rakeb syndrome MalaCards C3714552 Strength decreased C0747057 Organic heart disease UMLS C0015402 Hemorrhage eye C0038525 Subarachnoid hemorrhage HSDN C1263846 Attention deficit disorder with hyperactivity C0016667 Fragile x syndrome OrphaNet|HPO|MalaCards C0020305 Fetal edema C3489393 Hiatal hernia HSDN C0026838 Spasticity muscle C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C1963137 Hydrocephalus adverse event C3550904 Epileptic encephalopathy, early infantile, 36 MalaCards C0013362 Dysarthrias C1853250 Spinocerebellar ataxia 23 HPO C0018784 Deafness sensorineural C1848638 Usher syndrome, type ib (disorder) HPO C0341865 Headaches menopausal C0393735 Headache disorders UMLS C2237041 Shox gene with short stature C0265326 Bannayan-riley-ruvalcaba syndrome OrphaNet|HPO|MalaCards C0022346 Yellow skin C0013289 Duodenal diseases HSDN C4084727 Cough frequency C1836929 Emanuel syndrome MalaCards C0009460 Communication impairment C0038271 Stereotyped behavior HSDN C0034124 Pupillary disorder C0027743 Nerve compression syndrome HSDN C0497247 Blood pressure elevation C0235387 Porphyria type syndrome OrphaNet C3815497 Cough C0019348 Herpes simplex infections HSDN C0015300 Ocular proptosis C1860042 Antley-bixler syndrome with disordered steroidogenesis MalaCards C0857305 Thrombocytopenia purpura C1963234 Serum sickness adverse event HSDN C4084773 Bothered by weight gain C0012118 Infection by dictyocaulus, nos HSDN C0013428 Painful urination C1512738 Infiltrating bladder urothelial carcinoma, lipid-cell variant UMLS C0026884 Muteness C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards C4084766 Vomiting C0004277 Tooth attrition HSDN C0019214 Hepatosplenomegaly C1849320 Sandhoff disease, adult type HPO C0003467 Angst C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0030193 Sense of pain C0022362 Jaw diseases HSDN C0009398 Color vision defects C0020517 Hypersensitivity HSDN C2024878 Cardiovascular surgery result: dyspnea C0023487 Acute promyelocytic leukemia HSDN C0018681 Headache, cephalalgia C0563150 Catastrophization HSDN C0007758 Cerebellar ataxia C0024535 Malaria, falciparum HSDN C0018772 Deafness C1963198 Pancreatitis adverse event HSDN C0010200 Cough symptom C0854981 Stage iii large cell carcinoma of lung UMLS C4085210 Usual severity pain C0014179 Endometritis HSDN C2911645 Weight loss adverse event C0033805 Pseudohypoaldosteronism HSDN C1963091 Diarrhea adverse event C0020473 Hyperlipidemia HSDN C4085211 Pain distress question C0334082 Nevus, epidermal (disorder) OrphaNet C0018784 Deafness sensorineural C0031069 Familial mediterranean fever HSDN C0518090 Frequency of pain question C1963164 Lymphopenia adverse event HSDN C0267633 Appendiceal colic C0267613 Appendix disease UMLS C0042928 Paralysis vocal cord C0005967 Bone neoplasms HSDN C0424755 Fever symptoms C0007194 Hypertrophic cardiomyopathy HSDN C3541349 Syncope C3150733 Long qt syndrome 13 MalaCards|HPO C3539889 Pelvic pain increasing in severity C0005491 Biofeedback HSDN C0151908 Dry skin C1835492 Tooth agenesis, selective, 4 (disorder) MalaCards C0030232 Color loss C0686721 Babies shaken HSDN C4084767 Bothered by vomiting C0032266 Emphysema, intestinal HSDN C0557874 Global developmental delay C3551019 Choroideremia, deafness, and mental retardation MalaCards C2911645 Weight loss adverse event C0870082 Hyperkeratosis HSDN C0030193 Sense of pain C0010481 Cushing syndrome HSDN C0242670 Chronic vegetative state C0042830 Perception visual HSDN C2242996 Tingling C0034067 Pulmonary emphysema HSDN C2984058 Have pain C0024137 Lupus erythematosus, cutaneous HSDN C4085548 Usual severity dizziness C0597109 Nurse's role HSDN C0030193 Sense of pain C0006285 Bronchopneumonia HSDN C0007758 Cerebellar ataxia C1858583 Hemosiderosis, systemic, due to aceruloplasminemia HPO C0557874 Global developmental delay C2931764 Furlong syndrome MalaCards C0030552 Paralysis partial C0018767 Auditory sense HSDN C0013404 Respiratory difficulty C0019195 Hepatitis, viral, human HSDN C0004134 Dyssynergia C0338473 Neuroaxonal dystrophies HSDN C0020538 Hbp C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency OrphaNet|HPO C4084784 Diarrhea C0026782 Mumps vaccine HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0035435 Rheumatism HSDN C0151786 Weakness muscle C0026269 Mitral valve stenosis HSDN C4084775 Usual severity weight loss C0030330 Panniculitis, peritoneal HSDN C0036572 Convulsion C0016483 Food preferences HSDN C0011991 Loose stools C0009021 Clonorchiasis DiseaseOntology C0042963 Symptoms vomiting C0003615 Appendicitis DiseaseOntology|HSDN|MalaCards C2984058 Have pain C1336753 Thyroid lymphoma MalaCards C0020450 Hyperemesis gravidarum C0009946 Conversion disorder HSDN C0557874 Global developmental delay C1855861 Glycogen storage disease 0, liver MalaCards C1263846 Attention deficit disorder with hyperactivity C0003537 Aphasia MalaCards C0023012 Delay language C2674937 Chromosome 10q26 deletion syndrome MalaCards C0002624 Amnesia retrograde C0020659 Hypothalamic neoplasms HSDN C4085642 Level of joint stiffness C0027341 Nail-patella syndrome OrphaNet|HPO|MalaCards C0031911 Pigment deposition C0035304 Retinal degeneration MalaCards C4084768 Usual severity vomiting C0011616 Contact dermatitis HSDN C0000737 Abdomen pain C0795623 Hepatitis a vaccine, inactivated HSDN C0030552 Paralysis partial C1836544 Schindler disease, type i OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0004275 Attitude health HSDN C0019825 Voice hoarseness C0013423 Dystonia musculorum deformans HSDN C1961131 Cough adverse event C0009651 Conditioning operant HSDN C2911645 Weight loss adverse event C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C4085210 Usual severity pain C0036240 Response, satiety HSDN C2032396 Pelvic pain on the right C0206680 Mesothelioma, cystic HSDN C0019209 Large liver C0221036 Acrodermatitis enteropathica HPO C1963252 Tremor adverse event C0431399 Familial aplasia of the vermis MalaCards C0497247 Blood pressure elevation C3150733 Long qt syndrome 13 MalaCards|HPO C0007758 Cerebellar ataxia C0751038 Cockayne syndrome, type ii HPO C2237041 Shox gene with short stature C3280953 Hypertriglyceridemia, transient infantile MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1962983 Cataract adverse event HSDN C0860603 Anxiety symptom C0393584 Benign hereditary chorea HPO C0024031 Back pain lower back C0549567 Pigmentation disorders HSDN C0013404 Respiratory difficulty C0025345 Menstruation disturbances HSDN C0018772 Deafness C0262655 Recurrent urinary tract infection HSDN C3829611 Nausea frequency C0003467 Anxiety HSDN C0030193 Sense of pain C0002902 Anencephaly HSDN C4084726 Distress cough C1535917 Nipah virus infection MalaCards C1557397 Adverse event associated with pain C0037315 Sleep apnea syndromes HSDN C0042798 Vision dim C0342770 Fumarase deficiency MalaCards|HPO C0522224 Palsied C0018798 Congenital heart defects HSDN C0522224 Palsied C0010346 Crohn disease HSDN C0349588 Stature short C1849158 Insulin-like growth factor i, resistance to, due to increased binding protein HPO C0033377 Caudal displacement C0338078 Non-functioning pituitary gland neoplasm MalaCards C4084766 Vomiting C0025290 Aseptic meningitis HSDN C1549543 Administration method - pain C0024959 Maxillary sinusitis HSDN C0518090 Frequency of pain question C0010038 Corneal opacity HSDN C4084784 Diarrhea C0009440 Common bile duct diseases HSDN C3641756 Have diarrhea C0014848 Esophageal achalasia HSDN C0424755 Fever symptoms C0027092 Myopia HSDN C0042024 Urine incontinence C3146297 Study of behavior during childhood HSDN C0349588 Stature short C1846331 Juvenile-onset dystonia MalaCards C4085317 Diarrhea frequency C0162538 Immunoglobulin a deficiency (disorder) HSDN C0039870 Leanness C0034885 Rectal neoplasms HSDN C3665492 Pigmentations C0155359 Scleral staphyloma MalaCards C3641755 Have constipation C0009241 Cognition disorders HSDN C0015672 Decreased energy C3665349 Secondary hypothyroidism OrphaNet|MalaCards C4084768 Usual severity vomiting C0025281 Meniere disease HSDN C4085222 Nausea C0015927 Intrauterine fetal demise HSDN C2132198 Abnormal blistering of the skin C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C0005745 Blepharoptosis C0265328 Alopecia-epilepsy-oligophrenia syndrome MalaCards C0151786 Weakness muscle C3714514 Infection HSDN C0042963 Symptoms vomiting C0013264 Muscular dystrophy, duchenne HSDN C0015300 Ocular proptosis C0265449 Pallister-killian syndrome MalaCards C3665347 Vision impaired C1969562 Mental retardation, autosomal dominant 1 HPO C0151889 Reflexes tendon increased C1970180 Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation HPO C0497406 Over weight C2827407 Infectious otitis media HSDN C0038002 Spleen enlargement C3280953 Hypertriglyceridemia, transient infantile MalaCards C1963071 Back pain adverse event C1000483 Genus anemia HSDN C1557397 Adverse event associated with pain C0001969 Alcoholic intoxication HSDN C0036572 Convulsion C0278878 Adult glioblastoma UMLS C0018772 Deafness C3489413 Lipomatosis, multiple HSDN C1963281 Vomiting adverse event C0004052 Aspiration of vomitus HSDN C0042963 Symptoms vomiting C0027743 Nerve compression syndrome HSDN C0041834 Erythematous condition C0432328 Xeroderma pigmentosum, variant form MalaCards C4085317 Diarrhea frequency C0038459 Equine strongyle infection HSDN C0557874 Global developmental delay C1414025 Dgcr gene HPO C1836296 Lower extremity weakness C0398746 Gluthathione synthetase deficiency MalaCards C4084768 Usual severity vomiting C0005416 Biliary dyskinesia HSDN C4085661 Usual severity nausea C0038828 Arteriomesenteric duodenal ileus HSDN C0557874 Global developmental delay C0265205 Robinow syndrome MalaCards|HPO C0151908 Dry skin C0553578 Non-bullous ichthyosiform erythroderma MalaCards C4084742 Bothered by night sweats C0032749 Post-kala-azar dermal leishmaniasis MalaCards C0002962 Angina C0009244 Behavioral cognitive therapy HSDN C2010774 Generalized convulsions occurring with high fever C0234533 Generalized seizures UMLS C0042571 Vertigo subjective C0037315 Sleep apnea syndromes HSDN C1963252 Tremor adverse event C1968561 Xeroderma pigmentosum, type g-cockayne syndrome HPO C1000483 Genus anemia C0020630 Hypophosphatasia OrphaNet|MalaCards C0242936 Center pain C0033595 Prostitution HSDN C0033774 Skin pruritus C0345985 Skin neoplasm keratoacanthoma eruptive MalaCards C2919142 Short stature adverse event C1856113 Mowat-wilson syndrome OrphaNet|HPO|MalaCards C0019209 Large liver C1834929 Congenital microgastria and limb reduction defects MalaCards C4084773 Bothered by weight gain C0033289 Family relationship, professional HSDN C0009421 Comatose C0004610 Bacteremia HSDN C3887638 Failure to thrive in infant C0042870 Vitamin d deficiency HSDN C2911645 Weight loss adverse event C0014170 Endometrial neoplasms HSDN C0042571 Vertigo subjective C2984291 Glioblastoma multiforme pathway HSDN C1963087 Constipation adverse event C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C4084769 Vomiting frequency C0021831 Intestinal diseases HSDN C0027066 Myoclonic jerking C0012746 Dissociative disorder HSDN C0026821 Cramp C0019163 Hepatitis b HSDN C0018772 Deafness C0036341 Schizophrenia HSDN C0221263 Cafe au lait spot C3150674 Chromosome 15q24 deletion syndrome HPO C0024031 Back pain lower back C0021799 Interprofessional relations HSDN C2911647 Weight gain adverse event C0021053 Immune system diseases HSDN C1557397 Adverse event associated with pain C0029429 Osteochondrosis HSDN C0344315 Mood depressed C0795953 Masa syndrome (disorder) MalaCards C3539891 Pelvic pain to the rear C0033575 Prostatic diseases HSDN C0007758 Cerebellar ataxia C3887654 Polyarteritis nodosa, childhood-onset MalaCards C0018681 Headache, cephalalgia C1868598 Parietal foramina HPO|UMLS C0028738 Nystagmus C1833321 Chorioretinal atrophy, progressive bifocal OrphaNet|MalaCards C0022346 Yellow skin C0007453 Cattle disease HSDN C0003113 Anomia C0033906 Psychological theories HSDN C0018834 Brash C3151097 Meier-gorlin syndrome 2 MalaCards|HPO C0497406 Over weight C0034013 Precocious puberty HSDN C0020672 Body temperature decreased C0017638 Glioma HSDN C1549543 Administration method - pain C0001849 Aids dementia complex HSDN C0020673 Hypothermia (central) (local) C0000833 Abscess HSDN C0019214 Hepatosplenomegaly C1744558 T-lymphocyte deficiency MalaCards C0031911 Pigment deposition C1333280 Desmoplastic melanoma MalaCards C0020455 Hypergammaglobulinemia C0021368 Inflammation MalaCards C0016204 Fart C0019284 Diaphragmatic hernia HSDN C0600142 Flash hot C0700201 Dyssomnias HSDN C0557874 Global developmental delay C0432255 Geroderma osteodysplastica MalaCards|HPO C2237041 Shox gene with short stature C1834304 Amyotrophy, hereditary neuralgic MalaCards|HPO C0007758 Cerebellar ataxia C0039006 Swine--diseases HSDN C0010200 Cough symptom C0878555 Diffuse panbronchiolitis MalaCards|UMLS C0242936 Center pain C1134719 Invasive ductal breast carcinoma HSDN C0026838 Spasticity muscle C1550672 Specimen type - ulcer HSDN C0035232 Diaphragmatic paralysis C0206157 Myopathies, nemaline HSDN C2919142 Short stature adverse event C0432240 Stuve-wiedemann dysplasia OrphaNet|HPO C2096293 Ent surgical result ear vertigo C1963067 Atrial fibrillation adverse event HSDN C0018681 Headache, cephalalgia C0206719 Central neurocytoma OrphaNet|UMLS|MalaCards C0015672 Decreased energy C0034069 Pulmonary fibrosis HSDN C0000737 Abdomen pain C3273032 Lymphoepithelioma-like hepatocellular carcinoma UMLS C0221166 Paraparesis C0152276 Granulocytic sarcoma HSDN C4084766 Vomiting C0349231 Phobic anxiety disorder HSDN C0002170 Alopecia disorders C2751321 Macrocephaly, alopecia, cutis laxa, and scoliosis HPO C0020455 Hypergammaglobulinemia C0001175 Acquired immunodeficiency syndrome HSDN C2984058 Have pain C0015556 Fallopian tube diseases HSDN C0004093 Asthenia C0486537 Laboratory observation of character HSDN C0001707 Aerophagia C0001173 Adult pyloric stenosis HSDN C0027498 Nausea vomiting C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0033774 Skin pruritus C0861856 Bile duct colloid carcinoma UMLS C4084802 Usual severity diarrhea C0003864 Arthritis HSDN C0349588 Stature short C1865208 Anal atresia, hypospadias, and penoscrotal inversion MalaCards C0231528 Muscle pain generalized C0270958 Kocher-debre-semelaigne syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0029443 Osteomyelitis HSDN C4085642 Level of joint stiffness C1851286 Ectopia lentis isolated OrphaNet|HPO|MalaCards C0011168 Disorder deglutition C1850792 Congenital myasthenic syndrome ib MalaCards C2984058 Have pain C0006285 Bronchopneumonia HSDN C0344315 Mood depressed C0162532 Variegate porphyria MalaCards|HPO C4085317 Diarrhea frequency C0022890 Labyrinthine disorder HSDN C3463815 Feel fatigue C0009375 Colonic neoplasms HSDN C0015672 Decreased energy C0035042 Psychology and religion HSDN C0557874 Global developmental delay C1274789 Ligneous conjunctivitis OrphaNet|HPO|MalaCards C0030200 Intractable pain C0032962 Pregnancy complications HSDN C0004134 Dyssynergia C0555206 Chiari malformation type ii MalaCards|UMLS C2024878 Cardiovascular surgery result: dyspnea C0026948 Mycosis fungoides HSDN C2911645 Weight loss adverse event C1546747 Specimen source codes - polyps HSDN C0018681 Headache, cephalalgia C0040128 Thyroid diseases HSDN C0850758 Pain pelvic C0205788 Histiocytoid hemangioma HSDN C3641756 Have diarrhea C1261473 Sarcoma HSDN C0024031 Back pain lower back C0002878 Anemia, hemolytic HSDN C3898969 Have been vomiting C1959626 Mevalonic aciduria MalaCards|HPO C2032395 Pelvic pain on the left C1704436 Peripheral arterial diseases HSDN C2237041 Shox gene with short stature C2936502 Charge syndrome, familial MalaCards C4084768 Usual severity vomiting C0162666 Mitochondrial encephalomyopathies HSDN C1963154 Renal failure adverse event C0221204 Lytic lesion MalaCards C1963281 Vomiting adverse event C0460137 Push down or depress HSDN C2024878 Cardiovascular surgery result: dyspnea C2239253 Aneurysm of sinus of valsalva MalaCards C0018772 Deafness C0029125 Optic atrophies, hereditary HSDN C0427055 Face weakness C3552335 Myasthenic syndrome, congenital, 12 UMLS C0518090 Frequency of pain question C0002949 Aneurysm, dissecting HSDN C0018772 Deafness C1858840 Deafness, autosomal recessive 20 MalaCards C0018772 Deafness C0010308 Congenital hypothyroidism MalaCards|HSDN C1963281 Vomiting adverse event C0003463 Anus neoplasms HSDN C3665492 Pigmentations C0027155 Myxosarcoma MalaCards C1963065 Apnea adverse event C0035243 Respiratory tract infections HSDN C0010200 Cough symptom C0085183 Neoplasms, second primary HSDN C1549543 Administration method - pain C0028432 Nose diseases HSDN C0917801 Sleep disorder insomnia C1291710 Disturbances of affect UMLS C0270948 Neurogenic muscular atrophy C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0012833 Dizzy C0524620 Metabolic syndrome x HSDN C4084802 Usual severity diarrhea C0027540 Necrosis HSDN C0039870 Leanness C0023890 Liver cirrhosis HSDN C1549543 Administration method - pain C0026277 Mixed salivary gland tumor HSDN C4084724 Usual severity constipation C0221069 Anterior spinal artery syndrome HSDN C0038002 Spleen enlargement C0221036 Acrodermatitis enteropathica HPO C4084784 Diarrhea C0041408 Turner syndrome HSDN C1384666 Decreased hearing C2931246 Chromosome 17, trisomy 17p11 2 MalaCards|HPO C3887873 Hearing loss C0009207 Cockayne syndrome HSDN C3887638 Failure to thrive in infant C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C0013604 Edematous C0042143 Uterine rupture HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3665624 Serum calcium below normal HSDN C0013362 Dysarthrias C1720777 Functional laterality HSDN C1279888 Proteinuria of undiagnosed cause C0013289 Duodenal diseases HSDN C0028643 Sensation loss C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C1000483 Genus anemia C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards C4084776 Weight loss C0007820 Cerebrovascular disorders HSDN C3539022 Pelvic pain decreasing in severity C0001261 Actinomycosis HSDN C0270948 Neurogenic muscular atrophy C2931821 Nakamura osame syndrome MalaCards C0023530 Leukopenia C1135161 Stage 4s neuroblastoma MalaCards C2984058 Have pain C0025295 Meningitis, pneumococcal HSDN C0018772 Deafness C2117411 X-ray of toe: syndactyly HSDN C0242936 Center pain C0011303 Demyelinating diseases HSDN C2919142 Short stature adverse event C2937419 Chromosome x pentasomy OrphaNet|MalaCards C0522224 Palsied C0085433 Acquired joint deformities HSDN C2984058 Have pain C0009353 Colles' fracture HSDN C0030794 Pelvis pain C0796561 Melanoma vaccines HSDN C0042798 Vision dim C0019562 Von hippel-lindau syndrome OrphaNet|HSDN|HPO|MalaCards C0007859 Pain neck C0031154 Peritonitis HSDN C0041657 Consciousness loss C1963067 Atrial fibrillation adverse event HSDN C1962972 Proteinuria adverse event C0013182 Drug allergy HSDN C0022107 Fussiness C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C1069915 Vertigo C0022116 Ischemia HSDN C0026826 High muscle tone C0024748 Alpha-mannosidosis HSDN C0019572 Hairiness C0001623 Adrenal gland hypofunction HSDN C0520587 Vulvovaginal discomfort C0152008 Disorder vulvovaginal UMLS C0349588 Stature short C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism OrphaNet|MalaCards C0019079 Bloody sputum C0032962 Pregnancy complications HSDN C1962956 Flatulence adverse event C0039082 Syndrome HSDN C0013362 Dysarthrias C0796561 Melanoma vaccines HSDN C0037315 Breathing disorder during sleeping C1862940 Amyotrophic lateral sclerosis, autosomal recessive HPO C1963170 Hypothermia adverse event C0042514 Tachycardia, ventricular HSDN C0033377 Caudal displacement C0162809 Kallmann syndrome MalaCards|HPO C1963077 Bone pain adverse event C0917715 Hajdu-cheney syndrome OrphaNet|HPO C4084727 Cough frequency C0014175 Endometriosis HSDN C0232466 Feeding difficulty C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0002965 Crescendo angina C0021053 Immune system diseases HSDN C0018772 Deafness C0029455 Osteopoikilosis (disorder) MalaCards C2911645 Weight loss adverse event C0025284 Meningeal neoplasms HSDN C2096293 Ent surgical result ear vertigo C0032285 Pneumonia HSDN C0026826 High muscle tone C0265428 9p+ syndrome MalaCards C0008031 Pain chest C0010823 Cytomegalovirus infections HSDN C4085549 Dizziness C0020522 Delayed hypersensitivity HSDN C0011991 Loose stools C0023223 Leg ulcer HSDN C0036572 Convulsion C0270831 Seizures, simple partial, special sensory symptoms UMLS C1963087 Constipation adverse event C0020875 Ileal diseases HSDN C3887638 Failure to thrive in infant C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C2024893 Cardiovascular surgery result: fatigue C0040558 Toxoplasmosis HSDN C4085862 Bothered by nausea C0017601 Glaucomas HSDN C0751495 Seizure focal C0393672 Benign psychomotor epilepsy, childhood UMLS C1963091 Diarrhea adverse event C2937287 Hematolysis HSDN C0239134 Cough productive C0694549 Community acquired pneumonia UMLS C4085862 Bothered by nausea C0403447 Chronic kidney insufficiency HSDN C4085661 Usual severity nausea C0795623 Hepatitis a vaccine, inactivated HSDN C0241137 Skin pallor C0007932 Chagas' disease + no organ inv MalaCards C0018681 Headache, cephalalgia C0043398 Yellow fever, urban MalaCards C1963281 Vomiting adverse event C0024117 Chronic obstructive airway disease HSDN C1961131 Cough adverse event C0021845 Intestinal perforation HSDN C4084802 Usual severity diarrhea C0023646 Lichen planus HSDN C3541349 Syncope C0001580 Adolescent behavior HSDN C4085222 Nausea C0027092 Myopia HSDN C0557874 Global developmental delay C3809609 Primary aldosteronism, seizures, and neurologic abnormalities MalaCards C0917816 Deficiency mental C1855081 Microcephaly, primary autosomal recessive, 1 MalaCards|HPO C0040485 Wryneck C1090821 Sepsis (invertebrate) HSDN C3539892 Pelvic pain in front C0010068 Coronary heart disease HSDN C0025222 Black stool C1274795 Urban schosser spohn syndrome MalaCards C3887638 Failure to thrive in infant C1850096 Pancreatic agenesis, congenital MalaCards|HPO C0013395 Indigestion C0236969 Substance-related disorders HSDN C0155552 Hearing loss mixed C0029878 Otitis externa HSDN C1557397 Adverse event associated with pain C0039520 Tenosynovitis HSDN C3641755 Have constipation C0034088 Pulmonary valve insufficiency HSDN C0018524 Hallucinate C0019151 Hepatic encephalopathy HSDN C4084724 Usual severity constipation C0206247 Amyloid neuropathies MalaCards C2919142 Short stature adverse event C0162530 Porphyria, erythropoietic HPO C0013395 Indigestion C0997768 Glaucoma HSDN C0042963 Symptoms vomiting C0342731 Deficiency of mevalonate kinase MalaCards C0085642 Asphyxia reticularis C0162871 Aortic aneurysm, abdominal HSDN C3539023 Pelvic pain increasing in frequency C2911643 Encounter due to family history of osteoporosis HSDN C4084766 Vomiting C0751161 Udpglucose 4-epimerase deficiency disease MalaCards|HPO C1549543 Administration method - pain C0027822 Neurodermatitis HSDN C4084773 Bothered by weight gain C2984330 Chagas disease pathway HSDN C0018681 Headache, cephalalgia C1336379 Stage ivb carcinoma of nasopharynx UMLS C0019086 Hemorrhagic ascites C0302149 Effusions serous UMLS C0027498 Nausea vomiting C0011311 Dengue fever MalaCards C0015672 Decreased energy C0002884 Hypochromic anemia HSDN C0231218 Malaise generalized C3273033 Well differentiated hepatocellular carcinoma UMLS C0271215 Blindness legal C1869115 Weill-marchesani syndrome, autosomal dominant HPO C0019209 Large liver C0342750 Glycogen storage disease type id MalaCards|HPO C0018772 Deafness C0004275 Attitude health HSDN C4084775 Usual severity weight loss C0036323 Schistosomiasis HSDN C4084725 Usual severity cough C0010414 Infection by cryptococcus neoformans HSDN C0162298 Stiffness joints C0024445 Lipomatosis, familial benign cervical OrphaNet|HPO|MalaCards C0009676 Confusion state C0037198 Sinus thrombosis, intracranial HSDN C0162834 Hyperpigmentation C0334082 Nevus, epidermal (disorder) OrphaNet C0424755 Fever symptoms C0035613 Rift valley fever OrphaNet|HSDN|MalaCards C0424755 Fever symptoms C0162557 Liver failure, acute HSDN C4085210 Usual severity pain C0042636 Vibrio infection HSDN C3539893 Pelvic pain occurs with intercourse C0023903 Liver neoplasms HSDN C4084776 Weight loss C0043325 Xanthomatosis HSDN C0038002 Spleen enlargement C0023788 Whipple disease OrphaNet|MalaCards C0242936 Center pain C1963120 Gynecomastia adverse event HSDN C4084723 Constipation C0037205 Sirenomelia HPO C2984058 Have pain C0006309 Brucellosis HSDN C0006370 Bulimia C0015397 Disorder of eye HSDN C0004604 Pain back C1868508 Kosenow syndrome MalaCards C0152116 Torticollis spasmodic C1857495 Cardiocranial syndrome MalaCards C4084774 Have weight loss C0037928 Spinal cord diseases HSDN C0042025 Urinary incontinence stress C0041971 Tumor urethra HSDN C0036572 Convulsion C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C0151686 Growth retardation C0403399 Finnish congenital nephrotic syndrome MalaCards|HPO C4084768 Usual severity vomiting C1855115 Methylmalonic aciduria, mut(0) type HPO C2315100 Pediatric failure to thrive C0795841 Jacobsen distal 11q deletion syndrome MalaCards C1963087 Constipation adverse event C3163620 Hypotension adverse event HSDN C0001707 Aerophagia C0525042 Feeding and eating disorders of childhood HSDN C3539023 Pelvic pain increasing in frequency C0010695 Cystocele HSDN C1549543 Administration method - pain C0033680 Protein-losing enteropathies HSDN C0015970 Fever unknown origin C0029443 Osteomyelitis HSDN C1963091 Diarrhea adverse event C0033700 Infection proteus HSDN C4084774 Have weight loss C0020255 Hydrocephalus HSDN C4042891 Sleep wake disorders C0795864 Smith-magenis syndrome HSDN C0557874 Global developmental delay C2751878 Hadziselimovic syndrome MalaCards C0231218 Malaise generalized C4055244 Childhood lymphomatoid granulomatosis UMLS C0013604 Edematous C1548777 Specimen reject reason - hemolysis HSDN C0018777 Deafness, conductive C2750080 Diamond-blackfan anemia 10 MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C1522133 High cholesterol level HSDN C0036659 Sensation disorder C1547046 Kind of quantity - taste HSDN C4084769 Vomiting frequency C0020676 Hypothyroidism HSDN C4085222 Nausea C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C0577564 Mass of lymphoreticular structure C0006413 Burkitt lymphoma UMLS C2132198 Abnormal blistering of the skin C2930812 Generalized elastolysis MalaCards C0151786 Weakness muscle C2931358 Muscular atrophy, spinal, infantile chronic form HPO C0015300 Ocular proptosis C1275081 Cardio-facio-cutaneous syndrome HPO C2881434 Unqualified visual loss, left eye, normal vision right eye C0015397 Disorder of eye UMLS C2911647 Weight gain adverse event C0042487 Venous thrombosis HSDN C0026858 Musculoskeletal pain C0022744 Knee injury HSDN C0039070 Collapse fleeting C0016045 Fibroma HSDN C3887638 Failure to thrive in infant C3150672 Arthrogryposis, renal dysfunction, and cholestasis 2 MalaCards|HPO C0020305 Fetal edema C0266015 Congenital digestive system anomalies HSDN C0036659 Sensation disorder C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C0242936 Center pain C0040261 Onychomycosis HSDN C2911647 Weight gain adverse event C0020541 Hypertension, portal HSDN C0033774 Skin pruritus C1548578 Location characteristic id - smoking HSDN C0032617 High urine output C0344315 Depressed mood HSDN C0000737 Abdomen pain C0016549 Foreign body reaction HSDN C2029884 Hearing loss by exam C0014121 Bacterial endocarditis HSDN C0016199 Pain flank C0162869 Aneurysm, ruptured HSDN C4084776 Weight loss C0206138 Crest syndrome MalaCards C0037383 Sneeze C0006015 Bordetella infections HSDN C0036396 Sciatica C0238154 Epidural hematoma HSDN C0030552 Paralysis partial C0011581 Depressive disorder HSDN C4085317 Diarrhea frequency C1548777 Specimen reject reason - hemolysis HSDN C3665347 Vision impaired C2931205 Usher syndrome, type 1a MalaCards C2700617 Irritation - emotion C0023521 Globoid cell leukodystrophy OrphaNet C0007758 Cerebellar ataxia C0268425 Alstrom syndrome HSDN C0034151 Hyperglobulinemic purpura C0027121 Myositis HSDN C4085862 Bothered by nausea C0019360 Herpes zoster disease HSDN C0018772 Deafness C0162309 Adrenoleukodystrophy MalaCards|HPO C3898969 Have been vomiting C2984572 Malaria pathway HSDN C4082202 Sleep quality question C0025427 Mercury poisoning OrphaNet|MalaCards C0017181 Gastrointestinal bleed C0543697 Mixed cryoglobulinemia MalaCards C0020538 Hbp C0342649 Vascular calcification MalaCards C0011991 Loose stools C0341268 Disorder of small intestine UMLS C3641755 Have constipation C1836704 Arrhythmogenic right ventricular dysplasia, familial, 7 MalaCards C0522224 Palsied C0010417 Cryptorchidism HSDN C0020455 Hypergammaglobulinemia C0018188 Granuloma HSDN C0023012 Delay language C0268228 Neuraminidase 1 deficiency OrphaNet C1549543 Administration method - pain C0043528 Zoonoses HSDN C0151818 Opisthotonos C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency OrphaNet|HPO|MalaCards C4085549 Dizziness C0031117 Peripheral neuropathy HSDN C0037316 Not enough sleeping C1830398 Grooming:-:point in time:^patient:- HSDN C0019079 Bloody sputum C0012602 Dirofilariasis HSDN C1860844 Sparse, thin hair C0265965 Dyskeratosis congenita OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0270327 Bedwetting HSDN C0020578 Hyperventilate C0021843 Intestinal obstruction HSDN C0030794 Pelvis pain C0034888 Rectal prolapse HSDN C0036572 Convulsion C3714262 Adnfle - autosomal dominant nocturnal frontal lobe epilepsy, non-refractory UMLS C2984057 Have nausea C0035066 Renal artery obstruction HSDN C0013404 Respiratory difficulty C0744098 Food allergy to shrimp UMLS C0042024 Urine incontinence C0393571 Multiple system atrophy HSDN C4084727 Cough frequency C0012644 Animal disease models HSDN C0004310 Auditory disorder process C0751813 Chronic brain injury HSDN C0233993 Sexuality related problems C0233999 Bigamy UMLS C2024893 Cardiovascular surgery result: fatigue C0948480 Coronary restenosis HSDN C1963086 Confusion adverse event C0751799 Brain hemorrhage, traumatic HSDN C0030193 Sense of pain C3838947 Infiltrating micropapillary breast carcinoma UMLS C0332563 Papulae C0347403 Benign cephalic histiocytosis OrphaNet|MalaCards C0036572 Convulsion C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C4085661 Usual severity nausea C3489393 Hiatal hernia HSDN C0015672 Decreased energy C0004763 Barrett esophagus HSDN C0023014 Developmental disorder language C2707011 Behavioral symptoms:-:point in time:^patient:- HSDN C0011991 Loose stools C0020523 Immediate hypersensitivity HSDN C0011206 Delirium acute C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C1860844 Sparse, thin hair C0795895 Acd-mental retardation syndrome OrphaNet|MalaCards C1000483 Genus anemia C1856465 Ghosal hematodiaphyseal dysplasia OrphaNet|HPO C4084769 Vomiting frequency C0016563 Form perception HSDN C0232513 Premature tooth loss C0030360 Papillon-lefevre disease MalaCards|HPO C2029884 Hearing loss by exam C0042075 Urologic diseases HSDN C3541349 Syncope C0004161 Athletic injuries HSDN C2029884 Hearing loss by exam C3280965 Congenital cataracts, hearing loss, and neurodegeneration MalaCards C0020615 Hypoglycemia nos C0024776 Maple syrup urine disease HPO C4084802 Usual severity diarrhea C0023343 Leprosy HSDN C0008031 Pain chest C1961100 Erectile dysfunction adverse event HSDN C0042025 Urinary incontinence stress C0023176 Lead poisoning HSDN C0043094 Weight gain C1962983 Cataract adverse event HSDN C0013604 Edematous C2751312 Bartter syndrome, type 4b HPO C0023012 Delay language C0853240 Mobius ii syndrome MalaCards C3665347 Vision impaired C3888098 Cataract, autosomal recessive congenital 1 MalaCards C0039070 Collapse fleeting C0011849 Diabetes mellitus HSDN C1279888 Proteinuria of undiagnosed cause C0015456 Facial dermatoses HSDN C0206160 Retic count elevated C0002351 Altitude sickness HSDN C0014591 Bleeding nose C0041466 Typhoid fever MalaCards C0018784 Deafness sensorineural C2750325 Oculootodental syndrome MalaCards C0030193 Sense of pain C0014061 Tick-borne encephalitis HSDN C0040822 D tremors C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards|UMLS C0013421 Dystonia C1850363 Niemann-pick disease, nova scotian type HPO C0231623 Femoral neuralgia C0154735 Lumbosacral plexus lesion, nos UMLS C4084725 Usual severity cough C0035956 Rupture spontaneous HSDN C0004604 Pain back C1261473 Sarcoma HSDN C0030200 Intractable pain C0334463 Malignant fibrous histiocytoma HSDN C1963249 Tinnitus adverse event C0700327 Clinical findings relating to memory HSDN C0086437 Joint hypermobility C1850386 Giant axonal neuropathy 1 MalaCards C0015469 Facial paralysis C0314657 Genetic predisposition HSDN C0242936 Center pain C0028431 Acquired nasal deformities HSDN C0003962 Ascites C1881600 Malignant vipoma MalaCards C2237041 Shox gene with short stature C1862103 Brachydactyly type c MalaCards|HPO C0156732 Edema or excessive weight gain in pregnancy nos C0028754 Obesity UMLS C1384666 Decreased hearing C0795864 Smith-magenis syndrome MalaCards|HPO C0015469 Facial paralysis C0007820 Cerebrovascular disorders HSDN C0000737 Abdomen pain C0151467 Addisonian crisis OrphaNet|MalaCards C4084776 Weight loss C0153463 Malig neop oth spec pancreas MalaCards C4084723 Constipation C0000771 Abnormalities, drug induced HSDN C0521763 Nystagmus produced by neck rotation C0028738 Nystagmus UMLS C0427054 Weakness of neck C0410179 Scleroatonic muscular dystrophy MalaCards C0015672 Decreased energy C0013720 Ehlers-danlos syndrome HSDN C3665347 Vision impaired C2316212 Cryopyrin-associated periodic syndromes MalaCards C0027497 Queasy C1332249 Ampulla of vater signet ring cell carcinoma UMLS C3898969 Have been vomiting C0024299 Lymphoma HSDN C0010200 Cough symptom C0520538 Tracheobronchopathia osteoplastica MalaCards C0038990 Sweats C3151476 Mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MalaCards|HPO C0023380 Lethargy C0032285 Pneumonia UMLS C4084767 Bothered by vomiting C0024299 Lymphoma HSDN C0424755 Fever symptoms C0025235 Melkersson-rosenthal syndrome MalaCards C0015672 Decreased energy C0038041 Spotted fevers DiseaseOntology|MalaCards C0003550 Broca aphasia C0003646 Aptitude HSDN C1963071 Back pain adverse event C0008149 Chlamydia infections HSDN C0857305 Thrombocytopenia purpura C3813607 Infantile gastroesophageal reflux HSDN C0027497 Queasy C0039590 Testicular neoplasms HSDN C3146279 Coma C0033923 Psychomotor function HSDN C4084769 Vomiting frequency C0019285 Diaphragmatic hernia traumatic HSDN C0332563 Papulae C4049638 Cutaneous small vessel vasculitis MalaCards C3887873 Hearing loss C0162309 Adrenoleukodystrophy MalaCards C0030552 Paralysis partial C0038016 Spondylolisthesis HSDN C0030794 Pelvis pain C0030455 Parametritis HSDN C0027498 Nausea vomiting C0751291 Desmoplastic medulloblastoma MalaCards C0013362 Dysarthrias C0206652 Cell sarcoma, small HSDN C0237326 Defecation pain C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C0349588 Stature short C1328931 Multiple lentigines MalaCards C0010038 Corneal opacity disorder C0878684 Short syndrome MalaCards C4084776 Weight loss C0013295 Duodenal ulcer HSDN C0742292 Chest pain char typical C0741025 Chest problem UMLS C0518090 Frequency of pain question C0036830 Serum sickness HSDN C3665492 Pigmentations C3463918 Embryonal cell carcinoma MalaCards C0000737 Abdomen pain C0036329 Schistosomiasis japonica DiseaseOntology C0018784 Deafness sensorineural C1832216 Bosley-salih-alorainy syndrome MalaCards|HPO C0497247 Blood pressure elevation C0300948 Caudal regression syndrome HPO C0015672 Decreased energy C0006107 Concussion HSDN C0013456 Pain ear C0038557 Submandibular gland diseases HSDN C0042571 Vertigo subjective C0270639 Lateral sinus thrombosis HSDN C0040485 Wryneck C0036341 Schizophrenia HSDN C4085661 Usual severity nausea C0031039 Effusion pericardial HSDN C0037763 Spasm C0040409 Tongue diseases HSDN C2029884 Hearing loss by exam C0007789 Cerebral palsy HSDN C0406402 Erythema fugax C0343065 Symptomatic dermographism UMLS C0150055 Pain chronic C0037932 Curvature of spine HSDN C4084726 Distress cough C0917875 Esophageal diverticulosis HSDN C0015230 Exanthem C0406353 Goldstein UMLS C0015672 Decreased energy C0549567 Pigmentation disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014461 Granuloma eosinophilic HSDN C0575081 Abnormal gait C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards C0424755 Fever symptoms C0032969 Pregnancy in diabetics HSDN C0557874 Global developmental delay C0034345 Pyruvate dehydrogenase complex deficiency disease OrphaNet|HPO|MalaCards C0013395 Indigestion C1656583 Rosacea HSDN C0264272 Nose discharge, purulent C0555970 Nasal infection UMLS C0518090 Frequency of pain question C0085073 Prosthesis-related infection HSDN C0234518 Speech slurred C1850510 Sialidosis, type i OrphaNet|HPO C3641755 Have constipation C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0030552 Paralysis partial C1881674 Medical device emits smoke HSDN C0019209 Large liver C2751643 Glycogen storage disease ixc MalaCards|HPO C1549543 Administration method - pain C0022593 Keratosis HSDN C4085211 Pain distress question C0023492 Leukemia, t-cell HSDN C4084775 Usual severity weight loss C0027643 Neoplasm recurrence, local HSDN C0877360 Bruxism aggravated C0006325 Bruxism UMLS C2984058 Have pain C0001249 Actinobacillus infections HSDN C0518090 Frequency of pain question C0025294 Meningococcal meningitis HSDN C0033774 Skin pruritus C1555914 Psychologist - psychotherapy, group HSDN C1963252 Tremor adverse event C0017178 Gastrointestinal diseases HSDN C0015468 Face pain C0017563 Gingival diseases HSDN C1279888 Proteinuria of undiagnosed cause C1704212 Embolism embolus HSDN C0018784 Deafness sensorineural C1832187 Deafness, autosomal dominant 12 HPO C4084776 Weight loss C0001349 Acute-phase reaction HSDN C4085210 Usual severity pain C0016879 Fusobacterium infections HSDN C0042024 Urine incontinence C0009375 Colonic neoplasms HSDN C0242936 Center pain C0027531 Neck injury HSDN C3463815 Feel fatigue C0027902 Neuropsychological diagnosis HSDN C0424755 Fever symptoms C0004239 Atrial flutter HSDN C0018681 Headache, cephalalgia C3897756 Recurrent childhood diffuse astrocytoma UMLS C0349588 Stature short C3887992 Thyrotropin-releasing hormone deficiency MalaCards C0023012 Delay language C3806412 Mgcph MalaCards C0015672 Decreased energy C1854896 Mucolipidosis iii gamma MalaCards C0019825 Voice hoarseness C0018024 Goiter, retrosternal HSDN C0151786 Weakness muscle C0342701 Transcobalamin ii deficiency MalaCards C1549543 Administration method - pain C1522137 Hypertriglyceridemia result HSDN C3203358 Alveolar hypoventilation C0032371 Poliomyelitis HSDN C2700617 Irritation - emotion C0520716 Pallidopontonigral degeneration HPO C2911645 Weight loss adverse event C0021818 Intervertebral disk displacement HSDN C3641756 Have diarrhea C0035920 Rubella HSDN C1963091 Diarrhea adverse event C0242634 Diseases primates HSDN C0242670 Chronic vegetative state C0036690 Septicemia HSDN C0027497 Queasy C0001173 Adult pyloric stenosis HSDN C0424755 Fever symptoms C1963215 Pneumothorax adverse event HSDN C1963247 Ventricular tachycardia adverse event C0340493 Paroxysmal familial ventricular fibrillation MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1854107 Hyperaldosteronism, familial, type ii MalaCards C1959630 Eye pain adverse event C0038325 Stevens-johnson syndrome HSDN C1963281 Vomiting adverse event C0023055 Laryngeal neoplasm HSDN C0042963 Symptoms vomiting C0004352 Autistic disorder HSDN C0241210 Speaking delay C0520719 Spinopontine atrophy MalaCards C0002962 Angina C0011127 Pressure ulcer HSDN C4084802 Usual severity diarrhea C0002874 Aplastic anemia HSDN C1963063 Anorexia adverse event C1963067 Atrial fibrillation adverse event HSDN C4085642 Level of joint stiffness C1850568 Nakajo syndrome MalaCards C0004134 Dyssynergia C1837713 Joubert syndrome 3 MalaCards|HPO|UMLS C0013604 Edematous C0014175 Endometriosis HSDN C2237041 Shox gene with short stature C0162283 Nephrogenic diabetes insipidus HPO C0020305 Fetal edema C2117329 X-ray of toe: polydactyly HSDN C4085211 Pain distress question C1546847 Entity name part type - family HSDN C0015469 Facial paralysis C0000833 Abscess HSDN C1145670 Failure respiratory C0008728 Churg-strauss syndrome MalaCards C4085211 Pain distress question C0517555 Venous thrombosis after immobility HSDN C0037316 Not enough sleeping C0011849 Diabetes mellitus HSDN C4084776 Weight loss C0024788 Green monkey virus disease OrphaNet|MalaCards C3641755 Have constipation C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C1963064 Anxiety adverse event C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C4084727 Cough frequency C0812393 Cancer patients and suicide and depression HSDN C4085210 Usual severity pain C0033680 Protein-losing enteropathies HSDN C4084767 Bothered by vomiting C0079731 B-cell lymphomas HSDN C1384606 Dyspareunia C1720830 Painful bladder syndrome OrphaNet|MalaCards C0403568 Pain during inflow of dialysate C1300028 Disorder characterised by pain UMLS C0005745 Blepharoptosis C0796032 Malpuech facial clefting syndrome MalaCards|HPO C3665492 Pigmentations C1527249 Colorectal cancer MalaCards C0042384 Vasculitis, nonspecific C0019250 Hereditary factor i deficiency disease MalaCards C0020615 Hypoglycemia nos C1856403 Etfb deficiencies HPO C0033790 Pseudobulbar palsy C0027149 Myxoma HSDN C0234376 Tremor action C1959582 Pten hamartoma tumor syndrome MalaCards C1999266 Depression adverse event C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 HPO C4085210 Usual severity pain C0043324 Juvenile xanthogranuloma HSDN C0018991 Paralysis one side of body C0238417 Scorpion sting HSDN C0033774 Skin pruritus C0005967 Bone neoplasms HSDN C0030975 Disorders perception C0037047 Sibling HSDN C2126095 Anterior right leg soft tissue swelling C0037580 Soft tissue swelling UMLS C0007758 Cerebellar ataxia C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C3539892 Pelvic pain in front C1550672 Specimen type - ulcer HSDN C0497406 Over weight C0019557 Hip fx HSDN C0015970 Fever unknown origin C0024110 Pulmonary abscess HSDN C4085210 Usual severity pain C0021359 Infertility HSDN C0857305 Thrombocytopenia purpura C0344311 Blister HSDN C0231835 Respiration rate increased C0342784 Pearson's marrow-pancreas syndrome HPO C3146279 Coma C0037313 Sleep HSDN C0241210 Speaking delay C0750927 Apraxia, developmental verbal HPO C0085631 Abnormal excitement C0013363 Dysautonomia HSDN C0917816 Deficiency mental C0796225 Mental retardation, x-linked 19 HPO C0030794 Pelvis pain C2911643 Encounter due to family history of osteoporosis HSDN C0033377 Caudal displacement C1845862 Creatine deficiency, x-linked MalaCards|HPO C0036572 Convulsion C1412397 Ancr gene HPO C3829611 Nausea frequency C0860603 Anxiety symptoms HSDN C0019214 Hepatosplenomegaly C0543669 Neutrophilia, hereditary MalaCards|HPO C0015230 Exanthem C0265962 Ichthyosis linearis circumflexa MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0034186 Pyelonephritis HSDN C0151786 Weakness muscle C0007097 Carcinomas HSDN C0917816 Deficiency mental C1859228 Cerebrohepatorenal syndrome, variant types HPO C1963274 Vasculitis adverse event C1866120 Autoimmune lymphoproliferative syndrome, type ib MalaCards|HPO C0009676 Confusion state C0029408 Degenerative polyarthritis HSDN C4085211 Pain distress question C0034895 Rectovaginal fistula HSDN C1963180 Neck pain adverse event C0019625 Sinus histiocytosis HSDN C4085549 Dizziness C0042170 Uveomeningoencephalitic syndrome HSDN C0037316 Not enough sleeping C0001973 Alcoholic intoxication, chronic HSDN C2203646 Jaundice C0001418 Adenocarcinoma HSDN C0002965 Crescendo angina C0039263 Takayasu arteritis HSDN C0036572 Convulsion C0036421 Systemic scleroderma MalaCards|HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0016510 Foot diseases HSDN C0013595 Eczematous dermatitis C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards C0018784 Deafness sensorineural C0042075 Urologic diseases HSDN C3898969 Have been vomiting C0041956 Ureteral obstruction HSDN C0036572 Convulsion C2750246 Pitt hopkins like syndrome 1 HPO C0150055 Pain chronic C1546847 Entity name part type - family HSDN C3887638 Failure to thrive in infant C3553512 Immunodeficiency, common variable, 8, with autoimmunity MalaCards C0008031 Pain chest C1334439 Adenoid cystic carcinoma of lung UMLS C0018772 Deafness C2937421 Prostatic hyperplasia HSDN C0917816 Deficiency mental C0796125 Pseudoprogeria syndrome MalaCards C0043094 Weight gain C0040196 Tick infestations HSDN C0040822 D tremors C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0013421 Dystonia C0002514 Amino acid metabolism, inborn errors HSDN C0011168 Disorder deglutition C0268247 Niemann-pick disease, type d MalaCards|HPO C1549543 Administration method - pain C0038271 Stereotyped behavior HSDN C3146279 Coma C0014060 Encephalitis, st. louis DiseaseOntology|HSDN|MalaCards C4084724 Usual severity constipation C1859049 Cchs with hirschsprung disease MalaCards|HPO C0028738 Nystagmus C1859301 Cerebellar hypoplasia with endosteal sclerosis MalaCards C0518090 Frequency of pain question C1546847 Entity name part type - family HSDN C0009398 Color vision defects C1412084 Abcd1 gene HSDN C0024031 Back pain lower back C0005944 Metabolic bone disorder HSDN C0013604 Edematous C0023473 Myeloid leukemia, chronic HSDN C1384666 Decreased hearing C1849432 Renal, genital, and middle ear anomalies OrphaNet|MalaCards C4085211 Pain distress question C0035358 Retroperitoneal neoplasm HSDN C1069915 Vertigo C0030319 Panic disorder HSDN C4084767 Bothered by vomiting C0006309 Brucellosis HSDN C3641756 Have diarrhea C0235387 Porphyria type syndrome OrphaNet C2096293 Ent surgical result ear vertigo C0007222 Cardiovascular diseases HSDN C0042963 Symptoms vomiting C0021051 Immunologic deficiency syndromes HSDN C0024031 Back pain lower back C0034067 Pulmonary emphysema HSDN C0242936 Center pain C0870082 Hyperkeratosis HSDN C3898969 Have been vomiting C1547044 Kind of quantity - smell HSDN C3146279 Coma C0038661 Suicide HSDN C0009792 Consciousness disorder C0460137 Push down or depress HSDN C2169806 Tic C0393576 Chorea acanthocytosis syndrome MalaCards|HPO|UMLS C0018775 Hearing loss bilateral C1548578 Location characteristic id - smoking HSDN C0013404 Respiratory difficulty C0264446 Cobaltosis UMLS C0917816 Deficiency mental C1860787 Down syndrome critical region HPO C0042384 Vasculitis, nonspecific C1866120 Autoimmune lymphoproliferative syndrome, type ib MalaCards|HPO C0012569 Double vision C1690964 Cataract HSDN C0460137 Push down or depress C0041408 Turner syndrome MalaCards C4042891 Sleep wake disorders C0039614 Tetanus HSDN C0019079 Bloody sputum C0270611 Brain damage HSDN C4084768 Usual severity vomiting C1548777 Specimen reject reason - hemolysis HSDN C0018681 Headache, cephalalgia C0729544 Fungal cns infection HSDN C2911647 Weight gain adverse event C0037274 Dermatologic disorders HSDN C4084768 Usual severity vomiting C1705714 Lats1 wt allele HSDN C4084726 Distress cough C0004161 Athletic injuries HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035204 Respiration disorders HSDN C0020458 Hyperhydrosis C0242287 Isaacs syndrome OrphaNet|HPO|MalaCards C0349588 Stature short C0265554 Ectrodactyly MalaCards C0522224 Palsied C0042345 Varicosity HSDN C0030193 Sense of pain C0013595 Eczema HSDN C0018681 Headache, cephalalgia C1335658 Radiation-induced intracranial meningioma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0018021 Goiter HSDN C0043094 Weight gain C0302280 Adrenogenital syndrome HSDN C3539023 Pelvic pain increasing in frequency C3244301 Coverage level - family HSDN C0270948 Neurogenic muscular atrophy C1850510 Sialidosis, type i OrphaNet|HPO C4084773 Bothered by weight gain C0152054 Therapeutic touch HSDN C0013595 Eczematous dermatitis C0030779 Pelger-huet anomaly MalaCards|HPO C0518090 Frequency of pain question C0034895 Rectovaginal fistula HSDN C0036572 Convulsion C3536587 Convulsive status epilepticus, refractory UMLS C0022346 Yellow skin C0023798 Lipoma HSDN C0024031 Back pain lower back C0003708 Arachnitis HSDN C0036572 Convulsion C0021308 Infarction HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0031046 Pericarditis HSDN C0036572 Convulsion C1855081 Microcephaly, primary autosomal recessive, 1 MalaCards|HPO C2911645 Weight loss adverse event C0032963 Pregnancy complications, cardiovascular HSDN C1549543 Administration method - pain C0206660 Germinoma HSDN C0242936 Center pain C0018021 Goiter HSDN C1279888 Proteinuria of undiagnosed cause C0023223 Leg ulcer HSDN C0235031 Neurological complaint C0152027 Sensory disorders UMLS C1963065 Apnea adverse event C0020598 Hypocalcemia HSDN C4085548 Usual severity dizziness C0002438 Amebiasis HSDN C4085317 Diarrhea frequency C0031117 Peripheral neuropathy HSDN C0018681 Headache, cephalalgia C0085315 Toxoplasmosis, cerebral UMLS C0026884 Muteness C0004782 Basal ganglia diseases HSDN C0042928 Paralysis vocal cord C0027888 Hereditary motor and sensory neuropathies HSDN C0015230 Exanthem C0748397 Reynolds syndrome OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0032851 Disease poultry HSDN C4085211 Pain distress question C0035801 Diseases rodent HSDN C4085211 Pain distress question C0242350 Erectile dysfunction HSDN C1963087 Constipation adverse event C0011581 Depressive disorder HSDN C4084724 Usual severity constipation C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards C1549543 Administration method - pain C0024693 Mandible injury HSDN C4085317 Diarrhea frequency C1456781 Benign melanocytic nevus HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1321581 Bezoar disorder HSDN C0424755 Fever symptoms C0024115 Lung diseases HSDN C0557874 Global developmental delay C2752008 Spastic paraplegia-50, autosomal recessive MalaCards|HPO C0022346 Yellow skin C0861861 Squamous cell bile duct carcinoma UMLS C0086565 Liver function abnormal C0043195 Subsepsis hyperergia syndrome MalaCards C0012833 Dizzy C0027658 Neoplasms, germ cell and embryonal HSDN C4084774 Have weight loss C0037369 Smoking HSDN C4049644 Depression C1868594 Perry syndrome OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C0027651 Tumor HSDN C0013404 Respiratory difficulty C0002994 Angioedema HSDN C2024878 Cardiovascular surgery result: dyspnea C0079504 Hermanski-pudlak syndrome MalaCards|HSDN C0040485 Wryneck C0027765 Nervous system disorder HSDN C0020505 Excessive eating C0206085 Kleine-levin syndrome MalaCards C1963071 Back pain adverse event C2937287 Hematolysis HSDN C0013604 Edematous C0019699 Hiv seropositivity HSDN C4085210 Usual severity pain C0040149 Subacute thyroiditis HSDN C0011991 Loose stools C0008384 Cholesterol ester storage disease OrphaNet|HPO C0220982 Keto acidosis C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C0086769 Panic attack C1854336 Paragangliomas 3 MalaCards C0030193 Sense of pain C0600518 Choroidal neovascularization HSDN C0027497 Queasy C3273031 Hnec MalaCards C0522224 Palsied C0000786 Spontaneous abortion HSDN C4049644 Depression C1858804 Cerebellar ataxia, deafness, and narcolepsy HPO C0033377 Caudal displacement C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0349588 Stature short C1863370 Saethre-chotzen syndrome with eyelid anomalies HPO C4084723 Constipation C1963215 Pneumothorax adverse event HSDN C0036572 Convulsion C0037579 Soft tissue neoplasms HSDN C0162834 Hyperpigmentation C1838329 Aplasia cutis congenita with epibulbar dermoids MalaCards C0003811 Cardiac rhythm disturbance C0041466 Typhoid fever OrphaNet|MalaCards C0004604 Pain back C0018081 Gonorrhea HSDN C0009806 Constipate C0024305 Lymphoma, non-hodgkin HSDN C0008031 Pain chest C0152018 Esophageal carcinoma OrphaNet|MalaCards C4042891 Sleep wake disorders C0232488 Abdominal colic HSDN C4084727 Cough frequency C1540912 Hypereosinophilic syndrome HSDN C0042571 Vertigo subjective C0007282 Carotid stenosis HSDN C0036396 Sciatica C0038356 Stomach neoplasms HSDN C0042798 Vision dim C0268360 Osteogenesis imperfecta, recessive perinatal lethal OrphaNet C0042963 Symptoms vomiting C1336856 Anaplastic carcinoma of extrahepatic bile duct UMLS C1963249 Tinnitus adverse event C0860603 Anxiety symptoms HSDN C0494475 Seizure generalized tonic clonic C3149074 Seizures, benign familial neonatal, 1 HPO C0013404 Respiratory difficulty C0009450 Disease caused by microorganism HSDN C0015672 Decreased energy C1704981 Hyperparathyroidism-jaw tumor syndrome OrphaNet|HPO C0039070 Collapse fleeting C0428977 Bradycardia UMLS C4084773 Bothered by weight gain C0021228 Variability of individual responses HSDN C2911645 Weight loss adverse event C0029456 Osteoporosis HSDN C4084802 Usual severity diarrhea C0086647 Mucopolysaccharidosis type iiia HPO C0023530 Leukopenia C2751630 Dursun syndrome HPO C3887638 Failure to thrive in infant C2750087 Bile acid malabsorption, primary MalaCards|HPO C0018524 Hallucinate C0033873 Psychiatry HSDN C0424755 Fever symptoms C0012817 Diverticulum HSDN C0042571 Vertigo subjective C0264766 Rheumatic mitral stenosis HSDN C4085210 Usual severity pain C0162832 Apc HSDN C0008031 Pain chest C1881674 Medical device emits smoke HSDN C4084775 Usual severity weight loss C0009917 Contracture HSDN C0040460 Dental pain C0011378 Dental leakage HSDN C0221170 Stiffness muscle C1868619 Paramyotonia congenita without cold paralysis HPO C3665492 Pigmentations C0038986 Sweat gland diseases MalaCards C1549543 Administration method - pain C0024591 Malignant hyperpyrexia due to anesthesia HSDN C4084774 Have weight loss C0013295 Duodenal ulcer HSDN C0018681 Headache, cephalalgia C0242707 Ventricular dysfunction, right HSDN C0234146 Absent reflex C0795910 Cowchock syndrome OrphaNet|HPO|MalaCards C0041834 Erythematous condition C0263313 Pemphigus foliaceus OrphaNet|MalaCards C3274924 Have been coughing C0001580 Adolescent behavior HSDN C0015672 Decreased energy C1866983 Scleroderma, familial progressive MalaCards C1961131 Cough adverse event C1963198 Pancreatitis adverse event HSDN C0002962 Angina C0013182 Drug allergy HSDN C1145670 Failure respiratory C0795814 Chromosome 6 ring syndrome OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C0006277 Bronchitis HSDN C0027497 Queasy C0036983 Septic shock HSDN C0018772 Deafness C1963229 Retinal detachment adverse event HSDN C0151908 Dry skin C0221056 Adult type dermatomyositis OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0032460 Polycystic ovary syndrome HSDN C4085862 Bothered by nausea C0021783 Internal external locus of control HSDN C0002622 Amnesias C0003811 Cardiac arrhythmia HSDN C0242936 Center pain C0030215 Palate tumor HSDN C0221263 Cafe au lait spot C0031511 Pheochromocytoma MalaCards|HSDN|HPO C0030193 Sense of pain C0036095 Salivary gland neoplasms HSDN C1279888 Proteinuria of undiagnosed cause C0221021 Microangiopathic hemolytic anemia MalaCards C0151786 Weakness muscle C3536983 Familial hypophosphatemic rickets HSDN C0002962 Angina C0043253 Trauma blunt HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0002312 Alpha-thalassemia HSDN C2096293 Ent surgical result ear vertigo C0010266 Cranial nerve diseases HSDN C0557874 Global developmental delay C0282512 Landau-kleffner syndrome MalaCards|HPO C0015469 Facial paralysis C0042133 Uterine fibroids HSDN C0857305 Thrombocytopenia purpura C0024228 Lymphatic diseases HSDN C3829611 Nausea frequency C0243026 Sepsis HSDN C0086565 Liver function abnormal C1865643 Cholestasis, progressive familial intrahepatic 3 HPO C4084775 Usual severity weight loss C0005586 Bipolar disorder HSDN C0234376 Tremor action C0391826 Lhermitte-duclos disease MalaCards|HPO C0917816 Deficiency mental C0242387 Mandibulofacial dysostosis MalaCards|HPO C0557874 Global developmental delay C1707400 Classic medulloblastoma MalaCards C0007758 Cerebellar ataxia C1844933 Spinocerebellar ataxia, x-linked 4 MalaCards C2096293 Ent surgical result ear vertigo C0005695 Bladder neoplasm HSDN C0018772 Deafness C0021390 Inflammatory bowel diseases HSDN C1549543 Administration method - pain C0024228 Lymphatic diseases HSDN C0000731 Abdomen distention C0024507 Majewski syndrome MalaCards C4084768 Usual severity vomiting C0344423 Atrial flutter by ecg finding HSDN C4084766 Vomiting C0008925 Cleft palate HSDN C0027796 Neuralgias C0033578 Prostatic neoplasms HSDN C0264272 Nose discharge, purulent C0149778 Soft tissue infections UMLS C0031911 Pigment deposition C3272841 Mutyh-associate polyposis MalaCards C0155344 Spasm of conjugated gaze C0344248 Horizontal spasm of gaze UMLS C0426579 Anorexia symptom C0036946 Sheep--diseases HSDN C1549543 Administration method - pain C0013592 Ectropion HSDN C0015230 Exanthem C0155262 Granulomas orbital UMLS C1384666 Decreased hearing C1833104 Diabetes mellitus, permanent neonatal MalaCards|HPO C0007758 Cerebellar ataxia C2751843 Leukoencephalopathy, cystic, without megalencephaly MalaCards|HPO C4084769 Vomiting frequency C0037928 Spinal cord diseases HSDN C0234132 Pyramidal sign C1866985 Early balding, patella luxation, acromicria, and hypogonadism MalaCards C4085211 Pain distress question C0206696 Carcinoma, signet ring cell HSDN C0020615 Hypoglycemia nos C0005956 Bone marrow diseases MalaCards C1557397 Adverse event associated with pain C0162637 Strongylida infections HSDN C0030554 Abnormal sensation C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C2984057 Have nausea C0232488 Abdominal colic HSDN C0159040 Skin texture changes C0406358 Recurr focal palmar peel UMLS C0413252 Hypothermia due to exposure C0026946 Mycoses HSDN C0007758 Cerebellar ataxia C2717957 Vasoplegia HSDN C4085549 Dizziness C0009241 Cognition disorders HSDN C4084766 Vomiting C0007124 Noninfiltrating intraductal carcinoma HSDN C0575081 Abnormal gait C0394006 Dysequilibrium syndrome OrphaNet|HPO C0018681 Headache, cephalalgia C0034067 Pulmonary emphysema HSDN C0242936 Center pain C0029463 Osteosarcoma OrphaNet|HSDN|HPO C0039870 Leanness C0024121 Lung neoplasms HSDN C3539893 Pelvic pain occurs with intercourse C0027765 Nervous system disorder HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0029184 Orbital fracture HSDN C4084802 Usual severity diarrhea C0018790 Cardiac arrest HSDN C0036572 Convulsion C0796117 Pitt syndrome MalaCards C4085210 Usual severity pain C0030849 Penile neoplasms HSDN C2984057 Have nausea C0010074 Coronary vessel anomalies HSDN C0018772 Deafness C2984572 Malaria pathway HSDN C1963093 Dizziness adverse event C0023895 Liver diseases HSDN C0018834 Brash C0268337 Ehlers-danlos syndrome, type 3 (disorder) HPO C0040485 Wryneck C0024689 Mandibular diseases HSDN C2984058 Have pain C0036879 Education sex HSDN C4085210 Usual severity pain C0027859 Acoustic neuroma HSDN C0013421 Dystonia C0004377 Automatism HSDN C0015672 Decreased energy C1707542 Cutaneous chronic lymphocytic leukemia UMLS C3665492 Pigmentations C0751690 Malignant peripheral nerve sheath tumor MalaCards C1549543 Administration method - pain C0030215 Palate tumor HSDN C4084897 Sleep disturbance subordinate domain C1847501 Glut1 deficiency syndrome MalaCards C4085210 Usual severity pain C1262206 Iliotibial band syndrome HSDN C0234533 Seizure generalized C0398568 Blood group deletion syndrome HPO C0007859 Pain neck C0038018 Spondylolysis HSDN C0007758 Cerebellar ataxia C1853554 Radiation induced meningioma MalaCards C0008031 Pain chest C0025222 Melena HSDN C0015672 Decreased energy C0006849 Oral candidiasis UMLS C4084776 Weight loss C0003838 Arterial occlusive diseases HSDN C1963249 Tinnitus adverse event C0037198 Sinus thrombosis, intracranial HSDN C0030554 Abnormal sensation C0034628 Radius fracture HSDN C0036572 Convulsion C1856974 Pontocerebellar hypoplasia type 4 (disorder) HPO|UMLS C0002624 Amnesia retrograde C1963138 Hypertension adverse event HSDN C0026821 Cramp C0021295 Infant, premature, diseases HSDN C0042963 Symptoms vomiting C0275911 Tuberculosis of intestines MalaCards C1963184 Nystagmus adverse event C3495588 Acrocephalopolydactylous dysplasia MalaCards C3662048 Sensation of burning or prickling of skin C0030554 Paresthesia UMLS C3274924 Have been coughing C4050613 Anxiety scale (basc-2) HSDN C0002963 Angina variant C0149931 Migraine disorders HSDN C0030552 Paralysis partial C0030920 Peptic ulcer HSDN C0027497 Queasy C0008775 Ciguatera poisoning HSDN C0009806 Constipate C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C0413252 Hypothermia due to exposure C0013080 Down syndrome HSDN C0041657 Consciousness loss C0001883 Airway obstruction HSDN C0036572 Convulsion C3554079 Combined oxidative phosphorylation deficiency 12 MalaCards|UMLS C1963063 Anorexia adverse event C0453996 Tobacco smoking HSDN C0000731 Abdomen distention C1292753 Primary effusion lymphoma OrphaNet|MalaCards C0018784 Deafness sensorineural C3203358 Hypoventilation MalaCards C0007758 Cerebellar ataxia C0265219 Miller dieker syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0021308 Infarction HSDN C4084802 Usual severity diarrhea C0035435 Rheumatism HSDN C0020455 Hypergammaglobulinemia C0015519 Factor x deficiency HSDN C2919142 Short stature adverse event C0342731 Deficiency of mevalonate kinase OrphaNet|HPO|MalaCards C0027497 Queasy C0520946 Emotional hypersensitivity HSDN C0028961 Urine output decreased C0042075 Urologic diseases HSDN C0026826 High muscle tone C3713418 Ppm-x syndrome MalaCards C4084766 Vomiting C0019557 Hip fx HSDN C2984058 Have pain C0015302 External exotoses HSDN C4084784 Diarrhea C0005940 Bone diseases HSDN C0497406 Over weight C0024535 Malaria, falciparum HSDN C0003862 Pain joint C0023234 Legg-calve-perthes disease OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0004030 Aspergillosis HSDN C0007758 Cerebellar ataxia C0268525 5-oxoprolinase deficiency MalaCards C3665347 Vision impaired C0265339 Borjeson-forssman-lehmann syndrome MalaCards|HPO C4020887 Photodysphoria C0271092 Progressive cone dystrophy (without rod involvement) OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C0919267 Ovarian neoplasm HSDN C3665492 Pigmentations C1857299 Retinal nonattachment, nonsyndromic congenital MalaCards C3146279 Coma C0011226 Hepatitis d infection DiseaseOntology|MalaCards C4084725 Usual severity cough C0162316 Iron deficiency anemia HSDN C4084768 Usual severity vomiting C0000809 Abortion, habitual HSDN C0008031 Pain chest C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C4084802 Usual severity diarrhea C0032269 Pneumococcal infections HSDN C0233762 Hallucinations auditory C0162531 Hereditary coproporphyria HPO C4084802 Usual severity diarrhea C0039240 Supraventricular tachycardia HSDN C0030193 Sense of pain C1333481 Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone UMLS C0007859 Pain neck C0001418 Adenocarcinoma HSDN C4084723 Constipation C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0013421 Dystonia C1279481 X-linked combined immunodeficiency diseases HSDN C4084767 Bothered by vomiting C2748608 Lead poisoning, susceptibility to HPO C3463815 Feel fatigue C0009395 Color perception HSDN C1963071 Back pain adverse event C0008065 Childhood behavior HSDN C0013604 Edematous C0085119 Foot ulcer HSDN C0007758 Cerebellar ataxia C0271972 Thiamine-responsive megaloblastic anemia MalaCards C4084768 Usual severity vomiting C0085423 Gram-negative bacterial infections HSDN C0020673 Hypothermia (central) (local) C0242966 Systemic inflammatory response syndrome HSDN C0024031 Back pain lower back C0702166 Acne HSDN C1963184 Nystagmus adverse event C1844777 Cone dystrophy, x-linked, 1 MalaCards|HPO C0028081 Night sweat C3273031 Hnec MalaCards C0235153 Sensory hallucination C1568249 Usher syndrome, type ii MalaCards|HPO C0851578 Disorder sleep C0005119 Bereavement HSDN C0008031 Pain chest C1546602 Specimen source codes - diverticulum HSDN C0917801 Sleep disorder insomnia C2936779 Hydroxymethylbilane synthase deficiency MalaCards C3274924 Have been coughing C0004623 Bacterial infections HSDN C2984058 Have pain C0036918 Sexually transmitted diseases, viral HSDN C0015672 Decreased energy C0001144 Acne vulgaris HSDN C0036572 Convulsion C0039373 Tay-sachs disease OrphaNet|UMLS|HPO|MalaCards C2315100 Pediatric failure to thrive C3554079 Combined oxidative phosphorylation deficiency 12 MalaCards C0011570 Monopolar depression C1568248 Usher syndrome, type iii MalaCards|HPO C1579931 Depressed - symptom C0041408 Turner syndrome MalaCards C0042963 Symptoms vomiting C0042076 Urologic neoplasms HSDN C0085631 Abnormal excitement C0013870 Electroconvulsive shock HSDN C2911647 Weight gain adverse event C0206172 Diabetic foot HSDN C0003862 Pain joint C0162531 Hereditary coproporphyria HPO C0012833 Dizzy C0015802 Femur fracture HSDN C0424755 Fever symptoms C0029132 Disorder of the optic nerve HSDN C1549543 Administration method - pain C4084971 Trachoma HSDN C4084802 Usual severity diarrhea C0014571 Epiphyses, slipped HSDN C2199592 Earache of right ear C0810000 Other ear and sense organ disorders UMLS C0851578 Disorder sleep C0016658 Fracture bone HSDN C0349588 Stature short C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0042798 Vision dim C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C1384666 Decreased hearing C0796154 Simpson-golabi-behmel syndrome, type 1 MalaCards C3539889 Pelvic pain increasing in severity C0001261 Actinomycosis HSDN C0497406 Over weight C0002395 Alzheimer's disease HSDN C0030552 Paralysis partial C0016522 Foramen ovale, patent HSDN C3539895 Pelvic pain occurs with bowel movement C0037286 Skin neoplasms HSDN C0015970 Fever unknown origin C0041312 Tuberculosis git nos HSDN C0026838 Spasticity muscle C0017168 Gastroesophageal reflux disease HSDN C0030193 Sense of pain C1443290 Complex regional pain syndrome type ii of lower limb UMLS C0240715 Perineal lump C0042995 Vulvar neoplasms UMLS C0242936 Center pain C0030849 Penile neoplasms HSDN C3898969 Have been vomiting C0268579 Propionic acidemia HPO C1963249 Tinnitus adverse event C0020538 Hypertensive disease HSDN C1963249 Tinnitus adverse event C0032268 Pneumocephalus HSDN C0034933 Abnormal reflexes C0037939 Spinal neoplasms HSDN C0019209 Large liver C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0000737 Abdomen pain C1336223 Stage iiib carcinoma of liver cells UMLS C2024893 Cardiovascular surgery result: fatigue C1704375 Hypophosphatemic rickets OrphaNet|HPO|MalaCards C0085631 Abnormal excitement C3888018 Congenital hyperinsulinism MalaCards C0036572 Convulsion C0013312 Dupuytren contracture HSDN C0036572 Convulsion C0085077 Sweet syndrome MalaCards C0018681 Headache, cephalalgia C0004404 Autosuggestion HSDN C0009676 Confusion state C0010054 Coronary arteriosclerosis HSDN C0000737 Abdomen pain C0038941 Incisional infection HSDN C0005745 Blepharoptosis C1863370 Saethre-chotzen syndrome with eyelid anomalies HPO C0011168 Disorder deglutition C1853566 Genitopatellar syndrome MalaCards|HPO C4085211 Pain distress question C0001349 Acute-phase reaction HSDN C1557397 Adverse event associated with pain C0024021 Loudness perception HSDN C0022346 Yellow skin C2827407 Infectious otitis media HSDN C0018772 Deafness C2677434 Orofacial cleft 11 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0836924 Thrombocytosis HSDN C2114287 Prepubertal vaginal bleeding C0567444 Nonmenstrual bleeding UMLS C4084784 Diarrhea C0042900 Vitiligo HSDN C3274924 Have been coughing C1263846 Attention deficit hyperactivity disorder HSDN C0030554 Abnormal sensation C0037005 Shoulder dislocation HSDN C0030794 Pelvis pain C0269106 Endosalpingiosis UMLS C3665347 Vision impaired C1864670 Neuronal ceroid lipofuscinosis, congenital MalaCards|HPO C4084788 Have dizziness C0036341 Schizophrenia HSDN C4085210 Usual severity pain C0022374 Jejunal neoplasms HSDN C0424755 Fever symptoms C0042995 Vulvar neoplasms HSDN C0038868 Supranuclear palsy progressive C0001889 Akinetic mutism HSDN C0013604 Edematous C0001627 Congenital adrenal hyperplasia HSDN C4084723 Constipation C0020437 Hypercalcemia HSDN C4084727 Cough frequency C0001973 Alcoholic intoxication, chronic HSDN C0036659 Sensation disorder C0024953 Maxilla fracture HSDN C4085862 Bothered by nausea C0036690 Septicemia HSDN C0036572 Convulsion C3897750 Recurrent childhood gliosarcoma UMLS C0042940 Disorder of voice C0006434 Burn injury HSDN C0162298 Stiffness joints C1860042 Antley-bixler syndrome with disordered steroidogenesis MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3812171 Bradycardia by ecg finding HSDN C0011991 Loose stools C1704212 Embolism embolus HSDN C0015230 Exanthem C0571504 Co-trimoxazole allergy UMLS C0454644 Delayed language development C1845366 Mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance MalaCards|HPO C0027796 Neuralgias C2984299 Asthma pathway HSDN C0018991 Paralysis one side of body C0085094 Head injury closed HSDN C4085317 Diarrhea frequency C0238027 Botulism, infantile MalaCards C1557397 Adverse event associated with pain C0007894 Cestode infections HSDN C0041657 Consciousness loss C1552262 Nurse practitioner - family HSDN C1963086 Confusion adverse event C3494506 Pseudohypoparathyroidism, type ia HPO C1962972 Proteinuria adverse event C0021051 Immunologic deficiency syndromes HSDN C4085317 Diarrhea frequency C0014547 Epilepsies, partial HSDN C1962972 Proteinuria adverse event C0040524 Septic toxemia HSDN C1963170 Hypothermia adverse event C0035126 Reperfusion injury HSDN C2029884 Hearing loss by exam C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C1963137 Hydrocephalus adverse event C0265232 Frontonasal dysplasia anomalad MalaCards C4085317 Diarrhea frequency C0005424 Biliary tract diseases HSDN C0033774 Skin pruritus C0003507 Aortic valve stenosis HSDN C0851578 Disorder sleep C0001144 Acne vulgaris HSDN C0917816 Deficiency mental C2931394 Katsantoni papadakou lagoyanni syndrome OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0019114 Hemosiderosis HSDN C1963170 Hypothermia adverse event C0002063 Alkalosis HSDN C0270948 Neurogenic muscular atrophy C1850674 Minicore myopathy with external ophthalmoplegia (disorder) MalaCards|HPO C3539890 Pelvic pain causes awakening at night C0024141 Lupus erythematosus, systemic HSDN C0036572 Convulsion C3494906 Myoclonic absence epilepsy, non-intractable UMLS C0031256 Petechia C0398738 Leukocyte adhesion deficiency type 1 MalaCards C1971624 Appetite absent C3495422 Finding relating to sexuality and sexual activity HSDN C0011991 Loose stools C0019322 Umbilical hernia HSDN C0042963 Symptoms vomiting C0022658 Kidney diseases HSDN C0427055 Face weakness C3809137 Muscular dystrophy, limb-girdle, type 2r MalaCards C0162275 Ketoaciduria C1855102 Methylmalonic aciduria cblb type HPO C4085211 Pain distress question C1306503 Congenital exomphalos HSDN C0232197 Fibrillation C1865864 Amyotrophic lateral sclerosis 5 MalaCards C3714552 Strength decreased C1969443 Trifunctional protein deficiency with myopathy and neuropathy UMLS C0557874 Global developmental delay C0268338 Ehlers-danlos syndrome, type iv OrphaNet|HPO C0018772 Deafness C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0018965 Blood urine C0027341 Nail-patella syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0302363 Bang disease MalaCards C0003811 Cardiac rhythm disturbance C1840378 Brachycephalofrontonasal dysplasia MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0027643 Neoplasm recurrence, local HSDN C4085211 Pain distress question C0009442 Common bile duct neoplasms HSDN C0424755 Fever symptoms C0010674 Cystic fibrosis HSDN C0030554 Abnormal sensation C0023518 Leukocytosis HSDN C1963087 Constipation adverse event C0019069 Hemophilia a HSDN C1961131 Cough adverse event C0011644 Scleroderma OrphaNet|MalaCards C4084726 Distress cough C0027643 Neoplasm recurrence, local HSDN C0151740 Intracranial hypertension C3714644 Thymus neoplasms MalaCards C0851578 Disorder sleep C2015933 Outcomes otolaryngology hearing HSDN C0152169 Colic renal C0001126 Renal tubular acidosis HSDN C0019209 Large liver C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C0013428 Painful urination C0017979 Glycosuria HSDN C4084768 Usual severity vomiting C0043019 Lateral medullary syndrome HSDN C1963252 Tremor adverse event C0795910 Cowchock syndrome MalaCards|HPO C0012569 Double vision C0037369 Smoking HSDN C0002962 Angina C0017926 Glycogen storage disease type vii HSDN C0727671 Red cross toothache drops C0079173 Craniomandibular disorders HSDN C0015230 Exanthem C0268389 Amyloidosis, familial visceral MalaCards|HPO C0344434 Atrial fibrillation ecg C0013481 Ebstein anomaly OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0032226 Pleural diseases HSDN C0007758 Cerebellar ataxia C1858854 Megalencephalic leukoencephalopathy with subcortical cysts HPO C0221184 Hemianopsia bitemporal C1334698 Meningothelial cell neoplasm MalaCards C1961131 Cough adverse event C0037356 Smallpox virus HSDN C0232493 Epigastric pain C2945767 Childhood liver cancer MalaCards C0033774 Skin pruritus C0001721 Emotional affect HSDN C4085661 Usual severity nausea C0010481 Cushing syndrome HSDN C3641755 Have constipation C0003838 Arterial occlusive diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040196 Tick infestations HSDN C0151825 Ostalgia C4085250 Paget disease of bone 6 UMLS C0039231 Heartbeats increased C1837014 Atrial fibrillation, familial, 3 MalaCards|HPO C2132198 Abnormal blistering of the skin C0162569 Hepatoerythropoietic porphyria MalaCards C2700617 Irritation - emotion C0268581 Holocarboxylase synthetase deficiency OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome MalaCards|HPO C0007166 Cardiac output decreased C0003467 Anxiety HSDN C1963077 Bone pain adverse event C0242292 Mccune-albright syndrome OrphaNet|HPO C0035229 Respiratory function impaired C0406645 Amyopathic dermatomyositis MalaCards C4084726 Distress cough C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C4085210 Usual severity pain C0005639 Bisexual behavior HSDN C0333410 Deep granuloma annulare C0553697 Granulomatous inflammation UMLS C3887638 Failure to thrive in infant C0175692 Johanson-blizzard syndrome OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0003723 Arbovirus infections HSDN C0027497 Queasy C0026848 Myopathy HSDN C0028738 Nystagmus C3807567 Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome MalaCards C0013456 Pain ear C0022893 Otitis interna HSDN C0032285 Pneum C1842763 Spondyloenchondrodysplasia with immune dysregulation MalaCards|HPO C0027066 Myoclonic jerking C0206255 Malaria vaccine HSDN C0018681 Headache, cephalalgia C0152264 Familial erythrocytosis OrphaNet|HPO|UMLS C1557397 Adverse event associated with pain C0393735 Headache disorders HSDN C4084773 Bothered by weight gain C0039231 Tachycardia HSDN C0015230 Exanthem C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome MalaCards C0237326 Defecation pain C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C0917816 Deficiency mental C0220742 Bixler christian gorlin syndrome MalaCards C0018808 Murmur C0001973 Alcoholic intoxication, chronic HSDN C0522224 Palsied C0014536 Epidural tumor HSDN C0030552 Paralysis partial C0007222 Cardiovascular diseases HSDN C0242936 Center pain C0043119 Werner syndrome HSDN C4085317 Diarrhea frequency C0037937 Spine injury HSDN C0086565 Liver function abnormal C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C0241210 Speaking delay C2931119 Mehes syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C1739395 Takotsubo cardiomyopathy HSDN C0751265 Learning disability C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards C0233514 Behavior abnormal C1849157 Insulin-like growth factor i, resistance to MalaCards C4085641 Level of joint pain C1845168 Hypophosphatemic rickets, x-linked recessive MalaCards C3665347 Vision impaired C0268365 Marfanoid hypermobility syndrome MalaCards C0085636 Light sensitivity C0265966 Hereditary benign intraepithelial dyskeratosis MalaCards C0234979 Dysdiadochokinesia C4225288 Short stature, microcephaly, and endocrine dysfunction UMLS C0015300 Ocular proptosis C0014461 Granuloma eosinophilic MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2004491 Cicatrix HSDN C2911647 Weight gain adverse event C0242350 Erectile dysfunction HSDN C2984058 Have pain C0042341 Varicocele HSDN C0022408 Disorder joint C1833454 Komuragaeri disease OrphaNet C0043068 Friderichsen-waterhouse syndrome C0020951 Immune complex diseases HSDN C0018681 Headache, cephalalgia C0149514 Bronchitis acute HSDN C0269671 Gestational edema without mention of hypertension C1290849 Disorder characterised by oedema UMLS C0019209 Large liver C1842836 Congenital disorder of glycosylation, type ii MalaCards|HPO C2073625 X-ray of chest: pleural effusion C1849554 Lymphangiectasia, pulmonary, congenital OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0009373 Colonic diseases HSDN C0023530 Leukopenia C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C0015672 Decreased energy C0029882 Otitis media HSDN C0040485 Wryneck C1527306 Spasmus nutans OrphaNet|MalaCards C0005745 Blepharoptosis C1848030 Hypotonia-cystinuria syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0342708 Gamma aminobutyric acid transaminase deficiency MalaCards|HPO C0221752 Rbc urine C0221021 Microangiopathic hemolytic anemia MalaCards C0015469 Facial paralysis C0036205 Sarcoidosis, pulmonary HSDN C4084767 Bothered by vomiting C0020625 Hyponatremia HSDN C0013595 Eczematous dermatitis C0268581 Holocarboxylase synthetase deficiency MalaCards C4084766 Vomiting C0947622 Cholecystolithiasis HSDN C2096293 Ent surgical result ear vertigo C0023530 Leukopenia HSDN C1963184 Nystagmus adverse event C1853925 Spondyloocular syndrome, autosomal recessive MalaCards|HPO C2032395 Pelvic pain on the left C0030455 Parametritis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1510428 Cerebral abscess HSDN C0700590 Diaphoresis excessive C0221032 Familial generalized lipodystrophy OrphaNet|HPO|MalaCards C0037763 Spasm C0016510 Foot diseases HSDN C0030200 Intractable pain C0080179 Vertebra fracture HSDN C0027497 Queasy C0242350 Erectile dysfunction HSDN C1856661 Cornea cloudy C0266526 Norrie disease MalaCards|HPO C0013428 Painful urination C0393911 Pure autonomic failure MalaCards C0398650 Idiopathic thrombocytopenia purpura C0009404 Colorectal neoplasms HSDN C0518090 Frequency of pain question C0026936 Mycoplasma infections HSDN C0162835 Hypopigmentation C1855772 Absent corpus callosum cataract immunodeficiency OrphaNet|HPO|MalaCards C0557874 Global developmental delay C1857252 2,4-dienoyl-coa reductase deficiency MalaCards C0013604 Edematous C0037051 Behavior illness HSDN C0242936 Center pain C1963148 Iron overload adverse event HSDN C0917816 Deficiency mental C0796045 Ataxia-deafness-retardation syndrome MalaCards C3887638 Failure to thrive in infant C0268416 Enterokinase deficiency MalaCards|HPO C3665492 Pigmentations C0268497 Brown oculocutaneous albinism MalaCards C1384666 Decreased hearing C0035920 Rubella HSDN C0018991 Paralysis one side of body C0041327 Tuberculosis, pulmonary HSDN C4085317 Diarrhea frequency C0013364 Dysautonomia, familial HPO C0278152 Hemifacial spasms C0015190 Euthyroid sick syndromes HSDN C4084725 Usual severity cough C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C4084767 Bothered by vomiting C0011603 Dermatitis HSDN C2024893 Cardiovascular surgery result: fatigue C0004935 Animal ethology HSDN C4050613 Anxiety C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0795956 Chylomicron retention disease MalaCards|HPO C0241210 Speaking delay C3553637 Hyperphosphatasia with mental retardation syndrome 2 MalaCards C0557874 Global developmental delay C0220767 Craniofrontonasal dysplasia HPO C4084766 Vomiting C0023470 Myeloid leukemia HSDN C0011991 Loose stools C0013364 Dysautonomia, familial HPO|UMLS C0042928 Paralysis vocal cord C0080178 Spina bifida HSDN C0042940 Disorder of voice C0042830 Perception visual HSDN C4084773 Bothered by weight gain C0007621 Neoplastic cell transformation HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0158328 Trigger finger HSDN C3665346 Loss sight C0339534 Usher syndrome type 2 OrphaNet|HPO|MalaCards C0349588 Stature short C3809233 Noonan syndrome 8 MalaCards C0002962 Angina C0041948 Uremia HSDN C0151786 Weakness muscle C2677843 Episodic ataxia, type 7 MalaCards C0030552 Paralysis partial C0007097 Carcinomas HSDN C0424755 Fever symptoms C0009495 Behavior, competitive HSDN C3541349 Syncope C0037929 Spinal cord injuries HSDN C0151889 Reflexes tendon increased C4012727 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 MalaCards C0085593 Chill C0026946 Mycoses HSDN C0522224 Palsied C0268450 Gitelman syndrome MalaCards|HSDN|HPO C1557397 Adverse event associated with pain C0032797 Postpartum hemorrhage HSDN C2919142 Short stature adverse event C2931928 Mitochondrial cytopathy MalaCards C3641756 Have diarrhea C2350521 Gustatory perception HSDN C0000727 Abdomen acute C0947622 Cholecystolithiasis HSDN C4084723 Constipation C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C1963281 Vomiting adverse event C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C3898969 Have been vomiting C3150679 Eoe2 MalaCards C4085317 Diarrhea frequency C1532560 Plasmacytoma - category HSDN C1963249 Tinnitus adverse event C0007774 Cerebral arterial diseases HSDN C1963086 Confusion adverse event C0004238 Atrial fibrillation HSDN C0039070 Collapse fleeting C0162526 Aids-related opportunistic infections HSDN C3541349 Syncope C4050613 Anxiety scale (basc-2) HSDN C0003862 Pain joint C3540852 Rickets, x-linked hypophosphatemic MalaCards C0428977 Pulse rate decrease C0342623 Senile systemic amyloidosis MalaCards C1963086 Confusion adverse event C0039483 Giant cell arteritis HSDN C0017181 Gastrointestinal bleed C0019099 Hemorrhagic fever, crimean MalaCards C0041657 Consciousness loss C0460137 Push down or depress HSDN C0151786 Weakness muscle C0160680 Carotid artery injury HSDN C3665347 Vision impaired C1846980 Senior-loken syndrome 3 MalaCards C0009792 Consciousness disorder C0497327 Dementia HSDN C0018772 Deafness C0006434 Burn injury HSDN C0026838 Spasticity muscle C1704972 Genomic orientation HSDN C0004134 Dyssynergia C0344488 Absence; cerebellum OrphaNet C4085548 Usual severity dizziness C0036864 Sexual relations HSDN C0262527 Intermittent abdominal pain C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C0917816 Deficiency mental C2678046 Mental retardation, x-linked, syndromic, turner type OrphaNet|HPO C4085210 Usual severity pain C0001768 Agammaglobulinemia HSDN C1963137 Hydrocephalus adverse event C1856052 Game friedman paradice syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C2981150 Uranostaphyloschisis HSDN C0011991 Loose stools C0018824 Heart valve disease HSDN C0011991 Loose stools C0206171 Community acquired infections HSDN C3898969 Have been vomiting C4049994 Insulin resistance measurement HSDN C0234512 Prosopagnosia C0270611 Brain damage HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1412004 Tumor of the pineal region HSDN C0043094 Weight gain C0026850 Muscular dystrophy HSDN C4084769 Vomiting frequency C0029456 Osteoporosis HSDN C0042024 Urine incontinence C0015745 Ingestive behavior HSDN C4084784 Diarrhea C1532560 Plasmacytoma - category HSDN C0011206 Delirium acute C1963067 Atrial fibrillation adverse event HSDN C0020455 Hypergammaglobulinemia C0007134 Renal cell carcinoma HSDN C0002622 Amnesias C1290398 Cerebral arterial aneurysm HSDN C3898969 Have been vomiting C0279606 Childhood hepatocellular carcinoma MalaCards C4084784 Diarrhea C0011633 Dermatomyositis HSDN C2984057 Have nausea C0023055 Laryngeal neoplasm HSDN C0002962 Angina C0009319 Colitis HSDN C0406146 Meningococcal rash C0406680 Systemic diseases affecting skin UMLS C0851578 Disorder sleep C0006277 Bronchitis HSDN C0424755 Fever symptoms C0542241 Toxemia bacterial HSDN C0151908 Dry skin C0265201 De sanctis-cacchione syndrome MalaCards C3274924 Have been coughing C0037939 Spinal neoplasms HSDN C0024031 Back pain lower back C0030922 Peptic ulcer hemorrhage HSDN C3887638 Failure to thrive in infant C0268630 Hyper-beta-alaninemia MalaCards C1963281 Vomiting adverse event C0034531 Experimental radiation injuries HSDN C4084767 Bothered by vomiting C0016989 Galvanic skin response HSDN C1963252 Tremor adverse event C1857355 Leigh syndrome , french canadian type HPO C3641756 Have diarrhea C0032914 Pre-eclampsia HSDN C0013595 Eczematous dermatitis C2750747 Night blindness, congenital stationary, type 1c HPO C0013362 Dysarthrias C0007682 Cns disorder HSDN C0009421 Comatose C0023473 Myeloid leukemia, chronic HSDN C0023012 Delay language C0023014 Language development disorders MalaCards C3815497 Cough C0027819 Neuroblastoma HSDN C1000483 Genus anemia C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards C4084775 Usual severity weight loss C0006663 Calcinosis HSDN C4084802 Usual severity diarrhea C0020295 Hydronephrosis HSDN C0004134 Dyssynergia C0342731 Deficiency of mevalonate kinase OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0015745 Ingestive behavior HSDN C0018784 Deafness sensorineural C3714581 Multicystic dysplastic kidney HSDN C0344315 Mood depressed C0221033 Trisomy x syndrome MalaCards C0020450 Hyperemesis gravidarum C0156697 Hyperemesis gravidarum with metabolic disturbance - deliv UMLS C0018991 Paralysis one side of body C0546952 Congenital facial asymmetry HSDN C0027066 Myoclonic jerking C0276496 Familial alzheimer disease (fad) MalaCards C0231528 Muscle pain generalized C0023892 Biliary cirrhosis HSDN C3463815 Feel fatigue C0021361 Female infertility HSDN C0162323 Arthritis, multiple joint involvement C1836122 Sarcoidosis, early-onset MalaCards C4084767 Bothered by vomiting C0162576 Anisakiasis HSDN C1963065 Apnea adverse event C1837371 Sudden infant death with dysgenesis of the testes syndrome MalaCards|HPO C0557874 Global developmental delay C0011265 Presenile dementia MalaCards C4085210 Usual severity pain C1963139 Hypopigmentation adverse event HSDN C1963281 Vomiting adverse event C0085423 Gram-negative bacterial infections HSDN C0013604 Edematous C0439840 Reflex motion descriptor HSDN C0030554 Abnormal sensation C0206655 Alveolar rhabdomyosarcoma HSDN C0040264 Ear ringing sound C0007222 Cardiovascular diseases HSDN C4084775 Usual severity weight loss C0334533 Arteriovenous hemangioma HSDN C0522224 Palsied C0004775 Bartter disease HSDN C0007758 Cerebellar ataxia C0431399 Familial aplasia of the vermis MalaCards|HPO C1963063 Anorexia adverse event C0149573 Structure of posterior inferior cerebellar artery HSDN C0242670 Chronic vegetative state C0001973 Alcoholic intoxication, chronic HSDN C0015672 Decreased energy C0043346 Xeroderma pigmentosum OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0149778 Soft tissue infections HSDN C2700617 Irritation - emotion C0751435 Hyperphenylalaninaemia MalaCards C3274924 Have been coughing C0030807 Pemphigus, nos HSDN C4084766 Vomiting C0018621 Hay fever HSDN C0022346 Yellow skin C0948441 Venoocclusive disease MalaCards C3541349 Syncope C0042111 Urticaria pigmentosa HSDN C3463815 Feel fatigue C3489413 Lipomatosis, multiple HSDN C4042891 Sleep wake disorders C0006267 Bronchiectasis HSDN C0518090 Frequency of pain question C0041330 Tuberculosis, spinal HSDN C1557397 Adverse event associated with pain C0035795 Fever mountain rocky spotted HSDN C1549543 Administration method - pain C1610547 Production class code - pleasure HSDN C0013604 Edematous C0042594 Vestibular diseases HSDN C2919142 Short stature adverse event C0543816 Cardiocutaneous syndrome MalaCards C0851578 Disorder sleep C0002351 Altitude sickness HSDN C2024893 Cardiovascular surgery result: fatigue C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0023530 Leukopenia C3150751 Agammaglobulinemia 3, autosomal recessive HPO C0026821 Cramp C0007762 Cerebellar neoplasms HSDN C1999266 Depression adverse event C0017689 Glucagonoma MalaCards C0002962 Angina C0037999 Splenic neoplasms HSDN C0027066 Myoclonic jerking C0007350 Cat disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004935 Animal ethology HSDN C0042024 Urine incontinence C0079744 Diffuse large b-cell lymphoma HSDN C0018784 Deafness sensorineural C0034929 Reflex HSDN C4084767 Bothered by vomiting C0020544 Renal hypertension HSDN C0860603 Anxiety symptom C3711850 Opticospinal multiple sclerosis MalaCards C4084784 Diarrhea C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0162834 Hyperpigmentation C2673218 Brain tumor polyposis syndrome 2 (disorder) HPO C2029884 Hearing loss by exam C2931557 Chromosome 4 short arm deletion MalaCards C3496180 Sleep apnea C1862940 Amyotrophic lateral sclerosis, autosomal recessive HPO C1527344 Dysphonia C0023804 Lipomatosis, multiple symmetrical HSDN C0011991 Loose stools C0003504 Aortic valve insufficiency HSDN C1557397 Adverse event associated with pain C0015404 Eye infections, bacterial HSDN C0162835 Hypopigmentation C1865998 Odontotrichoungual-digital-palmar syndrome MalaCards C4084768 Usual severity vomiting C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO C0027498 Nausea vomiting C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C0522224 Palsied C3714644 Thymus neoplasms HSDN C0024902 Mastodynia C0243013 Base learn problems HSDN C0030193 Sense of pain C0751774 Nocturnal myoclonus syndrome HSDN C0031911 Pigment deposition C1333962 Hepatic angiomyolipoma MalaCards C0015402 Hemorrhage eye C0024961 Injuries maxillofacial HSDN C3146279 Coma C0017181 Gastrointestinal hemorrhage HSDN C4084723 Constipation C0040128 Thyroid diseases HSDN C0041834 Erythematous condition C0014805 Primary erythermalgia MalaCards C0332573 Macula C1148551 X-linked dyskeratosis congenita MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0031048 Pericarditis, constrictive HSDN C0013404 Respiratory difficulty C0697038 Asclepias tuberosa HSDN C0009080 Finger clubbing C1838121 Acrocardiofacial syndrome MalaCards C0518090 Frequency of pain question C0010403 Cryoglobulinemia HSDN C0575081 Abnormal gait C1333990 Hereditary nonpolyposis colorectal cancer MalaCards|HPO C0151908 Dry skin C0034960 Refsum disease OrphaNet|HPO C3665492 Pigmentations C0153422 Malig neop less curv stom unsp MalaCards C0004134 Dyssynergia C4015420 Epilepsy, progressive myoclonic 7 MalaCards C3539022 Pelvic pain decreasing in severity C0010068 Coronary heart disease HSDN C0026821 Cramp C0032851 Disease poultry HSDN C0857305 Thrombocytopenia purpura C0010823 Cytomegalovirus infections HSDN C4085211 Pain distress question C0037942 Spinal osteophytosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0002726 Amyloidosis HSDN C0027066 Myoclonic jerking C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO|UMLS C0038506 Stutter C0032787 Postoperative complications HSDN C0007166 Cardiac output decreased C0497327 Dementia HSDN C2024893 Cardiovascular surgery result: fatigue C0035579 Rickets HSDN C0004604 Pain back C0002453 Amenorrhea HSDN C0020505 Excessive eating C0021368 Inflammation HSDN C4085210 Usual severity pain C0085605 Liver failure HSDN C0002962 Angina C0016045 Fibroma HSDN C0151686 Growth retardation C2931280 Congenital alopecia, psychomotor retardation, convulsions OrphaNet C1557397 Adverse event associated with pain C0019348 Herpes simplex infections HSDN C0018834 Brash C0268353 Cutis laxa, x-linked MalaCards C0026826 High muscle tone C1851945 Dystonia 1, torsion, autosomal dominant OrphaNet|HPO|MalaCards C2984057 Have nausea C0036916 Sexually transmitted diseases HSDN C0018784 Deafness sensorineural C0268138 Xeroderma pigmentosum, complementation group d HPO C1963087 Constipation adverse event C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO C2203000 Weak hands and feet C2676767 Cd59 deficiency MalaCards|UMLS C0013421 Dystonia C0700327 Clinical findings relating to memory HSDN C2315100 Pediatric failure to thrive C0020598 Hypocalcemia HSDN C0013395 Indigestion C2711266 Infection by anisakis larva HSDN C0020538 Hbp C3276161 Arterial calcification, generalized, of infancy, 2 MalaCards C0332563 Papulae C0347404 Generalised eruptive histiocytoma MalaCards C0030193 Sense of pain C1000587 Pemphigus HSDN C0344434 Atrial fibrillation ecg C2678476 Cardiomyopathy, dilated, 1y MalaCards C1963170 Hypothermia adverse event C0033860 Psoriasis HSDN C0015938 Fetal macrosomia C0162482 Uterine inversion HSDN C0242936 Center pain C3809899 Episodic pain syndrome, familial, 3 MalaCards C0013362 Dysarthrias C1846582 Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration HPO C0026838 Spasticity muscle C4225170 Leukodystrophy, hypomyelinating, 13 UMLS C0012833 Dizzy C0038160 Staphylococcal infections HSDN C0018772 Deafness C0001126 Renal tubular acidosis HSDN C4084776 Weight loss C0022650 Kidney calculi HSDN C0031911 Pigment deposition C0751396 Well differentiated oligodendroglioma MalaCards C0027497 Queasy C0453996 Tobacco smoking HSDN C0024031 Back pain lower back C0020625 Hyponatremia HSDN C1963071 Back pain adverse event C3539923 Cdisc adas-cog - orientation summary score HSDN C0020580 Decreased sensation C0302148 Blood clot HSDN C2911647 Weight gain adverse event C1269683 Major depressive disorder HSDN C0242936 Center pain C0238417 Scorpion sting HSDN C0009676 Confusion state C2984289 Melanoma pathway HSDN C0007758 Cerebellar ataxia C0271375 Cranial nerve palsy iv trochlear HSDN C0240735 Personality change C0349275 Non-organic enduring personality change UMLS C0011991 Loose stools C1504665 Products used to treat diabetic ketoacidosis HSDN C0003811 Cardiac rhythm disturbance C0795947 Fryns-van den berghe syndrome OrphaNet|MalaCards C0022346 Yellow skin C0040034 Thrombocytopenia HSDN C2183443 Difficulty swallowing accompanied by pain C0011168 Deglutition disorders UMLS C1963252 Tremor adverse event C1837713 Joubert syndrome 3 MalaCards C2237041 Shox gene with short stature C0796206 Atkin syndrome OrphaNet|MalaCards C2984057 Have nausea C0037369 Smoking HSDN C4084802 Usual severity diarrhea C0017658 Glomerulonephritis HSDN C0036572 Convulsion C0038661 Suicide HSDN C2911645 Weight loss adverse event C0032269 Pneumococcal infections HSDN C2024878 Cardiovascular surgery result: dyspnea C0008479 Chondrosarcoma HSDN C1963184 Nystagmus adverse event C3888098 Cataract, autosomal recessive congenital 1 MalaCards C0030193 Sense of pain C0023281 Leishmaniasis HSDN C1963063 Anorexia adverse event C0002351 Altitude sickness HSDN C0010038 Corneal opacity disorder C2931187 Nephropathic cystinosis MalaCards C0231218 Malaise generalized C0392788 Nasal type extranodal nk/t-cell lymphoma UMLS C0026826 High muscle tone C0796123 Cataract-ataxia-deafness-retardation syndrome OrphaNet|MalaCards C4085211 Pain distress question C0024904 Mastoiditis HSDN C0085631 Abnormal excitement C0001175 Acquired immunodeficiency syndrome HSDN C0020305 Fetal edema C3150926 Anemia, congenital dyserythropoietic, type iv HPO C4084768 Usual severity vomiting C0002892 Anemia, pernicious HSDN C0026884 Muteness C1303073 Nicolaides baraitser syndrome MalaCards C0557874 Global developmental delay C2750785 Muscular dystrophy, congenital, lmna-related (disorder) OrphaNet|HPO C0020673 Hypothermia (central) (local) C0008325 Cholecystitis HSDN C0040264 Ear ringing sound C0006325 Bruxism HSDN C1000483 Genus anemia C0079474 Hallopeau-siemens disease HPO C0019209 Large liver C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C0004604 Pain back C0022116 Ischemia HSDN C0030232 Color loss C2750065 Retinitis pigmentosa, juvenile, lrat-related HPO C0575081 Abnormal gait C1835671 Axonal neuropathy with palmoplantar keratoderma MalaCards C0085636 Light sensitivity C0220701 Retinitis pigmentosa 1 MalaCards C1961131 Cough adverse event C0041316 Lymph node tuberculosis DiseaseOntology|MalaCards C1279888 Proteinuria of undiagnosed cause C0008065 Childhood behavior HSDN C4084724 Usual severity constipation C1866294 Ehlers-danlos syndrome, musculocontractural type 1 HPO C3146279 Coma C0036202 Sarcoidosis HSDN C0030552 Paralysis partial C0016057 Fibrosarcoma HSDN C1963252 Tremor adverse event C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0013395 Indigestion C0004610 Bacteremia HSDN C0036572 Convulsion C1303073 Nicolaides baraitser syndrome MalaCards|HPO C0030552 Paralysis partial C0040411 Tongue neoplasms HSDN C3665492 Pigmentations C3541517 Ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant MalaCards C0027796 Neuralgias C0018802 Congestive heart failure HSDN C1557397 Adverse event associated with pain C1546533 Specimen source codes - abscess HSDN C4084775 Usual severity weight loss C0042514 Tachycardia, ventricular HSDN C2919142 Short stature adverse event C1829813 Malonic acidemia MalaCards C1549543 Administration method - pain C0030807 Pemphigus, nos HSDN C0008031 Pain chest C0162869 Aneurysm, ruptured HSDN C0018991 Paralysis one side of body C0595812 Fistula route HSDN C0018524 Hallucinate C0013386 Dyskinesia, drug-induced HSDN C2183755 Diplopia in left eye only C0271190 Diplopia, unilateral UMLS C0043068 Friderichsen-waterhouse syndrome C1334928 Necrotic changes (finding) HSDN C0036572 Convulsion C4225237 Rhizomelic chondrodysplasia punctata, type 5 UMLS C0030552 Paralysis partial C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4084769 Vomiting frequency C0023895 Liver diseases HSDN C0011991 Loose stools C0028945 Oligodendroglioma HSDN C0012833 Dizzy C0024228 Lymphatic diseases HSDN C0085631 Abnormal excitement C0016399 Seizure focal motor HSDN C0008031 Pain chest C4050613 Anxiety scale (basc-2) HSDN C1963281 Vomiting adverse event C1548484 Rheumatic fever vaccine HSDN C0004134 Dyssynergia C0026946 Mycoses HSDN C0012833 Dizzy C0155490 Middle ear cholesteatoma HSDN C0011991 Loose stools C0032966 Complication, neoplastic pregnancy HSDN C0424755 Fever symptoms C0014852 Esophageal diseases HSDN C0018926 Emesis bloody C0021841 Intestinal neoplasms HSDN C3146279 Coma C0220710 Medium-chain acyl-coenzyme a dehydrogenase deficiency HPO C4085661 Usual severity nausea C0266836 Infantile colic HSDN C0151786 Weakness muscle C3280556 Peripheral neuropathy, myopathy, hoarseness, and hearing loss MalaCards C0027796 Neuralgias C0027746 Nerve degeneration HSDN C0015230 Exanthem C0277124 Cutaneous larva migrans by ancylostoma caninum UMLS C2024893 Cardiovascular surgery result: fatigue C0037050 Sick building syndrome HSDN C1546759 Specimen source codes - pustule C0014522 Epidermodysplasia verruciformis OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0002453 Amenorrhea HSDN C0518090 Frequency of pain question C0033847 Pseudoxanthoma elasticum HSDN C1959630 Eye pain adverse event C0018193 Granuloma, foreign-body HSDN C0020305 Fetal edema C0001080 Achondroplasia HSDN C3539020 Pelvic pain decreasing in frequency C0432264 Axial osteosclerosis MalaCards C0007758 Cerebellar ataxia C1527231 Adrenomyeloneuropathy MalaCards C4085661 Usual severity nausea C1720777 Functional laterality HSDN C1963180 Neck pain adverse event C0026769 Multiple sclerosis HSDN C0012569 Double vision C0206717 Olfactory neuroblastoma HSDN C0027498 Nausea vomiting C0022661 Kidney failure, chronic UMLS C2203646 Jaundice C0041324 Tuberculosis, osteoarticular HSDN C0039231 Heartbeats increased C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards C0040485 Wryneck C1860315 Whispering dysphonia, hereditary MalaCards C0026838 Spasticity muscle C0001173 Adult pyloric stenosis HSDN C0034155 Thrombotic thrombocytopenic purpura C0220847 C hepatitis virus HSDN C4084723 Constipation C0039231 Tachycardia HSDN C0007758 Cerebellar ataxia C0677607 Hashimoto disease HSDN C0004134 Dyssynergia C3281192 Infantile cerebellar-retinal degeneration MalaCards|UMLS C0700078 Deep tendon reflex decrease C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C2911645 Weight loss adverse event C2936881 Eosinophilic synovitis MalaCards C4085642 Level of joint stiffness C0029408 Degenerative polyarthritis MalaCards C4084723 Constipation C0036690 Septicemia HSDN C1963170 Hypothermia adverse event C0023434 Chronic lymphocytic leukemia HSDN C0034150 Skin purpura C0038325 Stevens-johnson syndrome HSDN C4084769 Vomiting frequency C0042138 Uterine neoplasms HSDN C0020672 Body temperature decreased C0007131 Non-small cell lung carcinoma HSDN C0518090 Frequency of pain question C0028758 Bonding HSDN C0162298 Stiffness joints C3151446 Nestor-guillermo progeria syndrome MalaCards|HPO|UMLS C0917816 Deficiency mental C1850140 Kaler garrity stern syndrome MalaCards C0393588 Dystonias paroxysmal C0338465 Sandifer syndrome UMLS C1549543 Administration method - pain C0008521 Choroid diseases HSDN C0036572 Convulsion C0270832 Absence, autonomic UMLS C2984057 Have nausea C0027663 Neoplasms, multiple primary HSDN C0413252 Hypothermia due to exposure C0002063 Alkalosis HSDN C0005745 Blepharoptosis C1838625 Warburg sjo fledelius syndrome HPO C0013362 Dysarthrias C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C2126045 Obstipation started suddenly C0221152 Obstipation UMLS C0018772 Deafness C0796232 Bohring syndrome MalaCards|HPO C0027066 Myoclonic jerking C0007959 Charcot-marie-tooth disease HSDN C0162298 Stiffness joints C0026706 Mucopolysaccharidosis iii OrphaNet|MalaCards C0013362 Dysarthrias C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0038506 Stutter C0004361 Autogenic therapy HSDN C0030193 Sense of pain C0276275 Disease due to parvoviridae HSDN C4085211 Pain distress question C0023269 Leiomyosarcoma HSDN C4084802 Usual severity diarrhea C2945560 Hemolytic HSDN C4084788 Have dizziness C0032914 Pre-eclampsia HSDN C0016204 Fart C1384606 Dyspareunia HSDN C0035232 Diaphragmatic paralysis C0520680 Sleep apnea, central HSDN C0037763 Spasm C0520946 Emotional hypersensitivity HSDN C0232466 Feeding difficulty C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C0028738 Nystagmus C1969053 Joubert syndrome 7 MalaCards|HPO C2984058 Have pain C0008074 Child development disorders, pervasive HSDN C1963180 Neck pain adverse event C0006107 Concussion HSDN C0035229 Respiratory function impaired C0271742 Glucocorticoid deficiency with achalasia HPO C4084775 Usual severity weight loss C0020097 Htlv-i infections HSDN C0040822 D tremors C0751039 Cockayne syndrome, type i HPO|UMLS C0000737 Abdomen pain C0032460 Polycystic ovary syndrome HSDN C4049644 Depression C0393639 Hashimoto's encephalitis MalaCards C0013404 Respiratory difficulty C0340231 Tracheobronchomalacia HSDN C0030794 Pelvis pain C1881674 Medical device emits smoke HSDN C1963184 Nystagmus adverse event C2677434 Orofacial cleft 11 MalaCards C1279888 Proteinuria of undiagnosed cause C0019621 Histiocytosis, langerhans-cell HSDN C1963093 Dizziness adverse event C0037937 Spine injury HSDN C4084768 Usual severity vomiting C0152724 Tuberculosis of intestines and mesenteric glands DiseaseOntology|MalaCards C0085636 Light sensitivity C1333359 Ercc5 gene HSDN C0349588 Stature short C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome MalaCards|HPO C0750394 Wbc low C0007965 Chediak-higashi syndrome MalaCards|HPO C0557874 Global developmental delay C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards C2911645 Weight loss adverse event C1963233 Seroma adverse event HSDN C0000737 Abdomen pain C2981402 Stage iiib colorectal cancer UMLS C0030794 Pelvis pain C0001580 Adolescent behavior HSDN C0015469 Facial paralysis C0028432 Nose diseases HSDN C3898969 Have been vomiting C0025281 Meniere disease HSDN C3539890 Pelvic pain causes awakening at night C0007621 Neoplastic cell transformation HSDN C1096250 Gastrointestinal discomfort C0020413 Hymenolepiasis DiseaseOntology C0018784 Deafness sensorineural C0043346 Xeroderma pigmentosum OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C1263846 Attention deficit disorder with hyperactivity C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C2029884 Hearing loss by exam C0022521 Kartagener syndrome HSDN C1963170 Hypothermia adverse event C0026266 Mitral valve insufficiency HSDN C4085210 Usual severity pain C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C3898969 Have been vomiting C0003618 Appetites HSDN C4084774 Have weight loss C0042029 Urinary tract infection HSDN C0231341 Aging premature C0034531 Experimental radiation injuries HSDN C3463815 Feel fatigue C0015745 Ingestive behavior HSDN C0018926 Emesis bloody C0027051 Myocardial infarction HSDN C0018681 Headache, cephalalgia C0796430 Adult choroid plexus tumor UMLS C0086565 Liver function abnormal C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C0036572 Convulsion C0348165 Viral cns infection HSDN C4084788 Have dizziness C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084784 Diarrhea C0025517 Metabolic diseases HSDN C4084725 Usual severity cough C0038160 Staphylococcal infections HSDN C0700078 Deep tendon reflex decrease C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0020672 Body temperature decreased C2936290 Femoracetabular impingement HSDN C0013404 Respiratory difficulty C1963090 Dehydration adverse event HSDN C0030193 Sense of pain C0206239 Cubital syndrome tunnel HSDN C0026838 Spasticity muscle C1290398 Cerebral arterial aneurysm HSDN C0518090 Frequency of pain question C0011649 Dermoid cyst HSDN C0520909 Ponv C0151744 Myocardial ischemia HSDN C0030552 Paralysis partial C0342784 Pearson's marrow-pancreas syndrome HPO C4084769 Vomiting frequency C0003864 Arthritis HSDN C0004134 Dyssynergia C0032787 Postoperative complications HSDN C0020450 Hyperemesis gravidarum C0032969 Pregnancy in diabetics HSDN C0018772 Deafness C0032269 Pneumococcal infections HSDN C0231835 Respiration rate increased C0334533 Arteriovenous hemangioma HSDN C0035021 Fever, famine C0152062 Spirillum minus DiseaseOntology|MalaCards C0013595 Eczematous dermatitis C1856251 Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i HPO C2911645 Weight loss adverse event C3150172 Mtdps8b MalaCards C2984058 Have pain C0340464 Heartbeats ectopic HSDN C0027066 Myoclonic jerking C0017636 Glioblastoma HSDN C2911647 Weight gain adverse event C0013418 Abnormal labor HSDN C0518090 Frequency of pain question C0002895 Anemia, sickle cell OrphaNet|MalaCards C0036572 Convulsion C0018920 Hemangioma, cavernous HSDN C2202732 Vulvar itching or burning C0406670 Burning vulva UMLS C0018772 Deafness C0027947 Neutropenia HSDN C1963237 Insomnia adverse event C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0232466 Feeding difficulty C0795889 Allan-herndon-dudley syndrome (ahds) MalaCards C0027497 Queasy C0026771 Trauma multiple HSDN C0008031 Pain chest C2350572 Illness behavior HSDN C2984058 Have pain C0023492 Leukemia, t-cell HSDN C0043094 Weight gain C3809877 Schaaf-yang syndrome MalaCards C3829611 Nausea frequency C1457883 Aggressive reaction HSDN C0020578 Hyperventilate C0087012 Ataxia, spinocerebellar HSDN C1557397 Adverse event associated with pain C0036220 Kaposi sarcoma HSDN C3539895 Pelvic pain occurs with bowel movement C0017412 Genital diseases, male HSDN C0460137 Push down or depress C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0023380 Lethargy C1847967 Ovarioleukodystrophy MalaCards|HPO C4085210 Usual severity pain C0005818 Blood platelet disorders HSDN C4042891 Sleep wake disorders C0014848 Esophageal achalasia HSDN C0030193 Sense of pain C1720149 Neuralgia associated with aids UMLS C1557397 Adverse event associated with pain C0028796 Dermatitis, occupational HSDN C0232943 Metromenorrhagia C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C1963177 Muscle pain adverse event C0043397 Yellow fever, jungle MalaCards C0039870 Leanness C0860549 Refeed syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0041341 Tuberous sclerosis HSDN C0476273 Distress respiratory C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate MalaCards|HPO C3887638 Failure to thrive in infant C0023418 Leukemia HSDN C4084727 Cough frequency C0001122 Acidosis HSDN C2911645 Weight loss adverse event C0027868 Neuromuscular diseases HSDN C3541349 Syncope C0009995 Cor triatriatum HSDN C4084774 Have weight loss C0268080 Hypercalcemia, idiopathic, of infancy HPO C0030193 Sense of pain C0027831 Neurofibromatosis 1 HSDN C0041657 Consciousness loss C0020459 Hyperinsulinism HSDN C1963184 Nystagmus adverse event C2674009 Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma MalaCards|HPO C0042798 Vision dim C0033923 Psychomotor function HSDN C4084766 Vomiting C1275081 Cardio-facio-cutaneous syndrome HPO C0700078 Deep tendon reflex decrease C3280845 Charcot-marie-tooth disease, dominant intermediate e MalaCards C0013378 Dysgensia C1552962 Units of measure - pica HSDN C3898969 Have been vomiting C0398623 Thrombophilia HSDN C0042025 Urinary incontinence stress C0000768 Congenital abnormality HSDN C1963184 Nystagmus adverse event C1857662 Coach syndrome OrphaNet|HPO|MalaCards C0014118 Inflammation of the heart valve C3542024 Aortic valve disease 2 MalaCards C0151786 Weakness muscle C0008626 Congenital chromosomal disease HSDN C0522224 Palsied C0032002 Pituitary diseases HSDN C4085317 Diarrhea frequency C1863239 Partial adenosine deaminase deficiency HPO C2919142 Short stature adverse event C1849348 Richieri costa pereira syndrome MalaCards|HPO C1971624 Appetite absent C1548578 Location characteristic id - smoking HSDN C0004134 Dyssynergia C1858114 Huntington disease-like 3 (disorder) MalaCards|UMLS C0039070 Collapse fleeting C0040028 Thrombocythemia, essential MalaCards C0015402 Hemorrhage eye C0086543 Cataract nos HSDN C4084766 Vomiting C0001430 Adenoma HSDN C0857305 Thrombocytopenia purpura C0027627 Neoplasm metastasis HSDN C0012569 Double vision C0007781 Intracranial embolism and thrombosis HSDN C3274924 Have been coughing C0006434 Burn injury HSDN C0017181 Gastrointestinal bleed C1414525 Fah gene HPO C4084802 Usual severity diarrhea C0950123 Inborn genetic disease HSDN C4085549 Dizziness C0001144 Acne vulgaris HSDN C2919142 Short stature adverse event C3810012 Rienhoff syndrome MalaCards C0004604 Pain back C1546654 Specimen source codes - granuloma HSDN C4084774 Have weight loss C1861172 Venous thromboembolism HSDN C3274924 Have been coughing C0018800 Cardiomegaly HSDN C4084802 Usual severity diarrhea C0006145 Breast diseases HSDN C1963087 Constipation adverse event C0153653 Malignant tumor of parathyroid gland MalaCards C0004134 Dyssynergia C0021843 Intestinal obstruction HSDN C0013604 Edematous C0017105 Clostridial myonecrosis HSDN C0522224 Palsied C0029456 Osteoporosis HSDN C0042963 Symptoms vomiting C0232600 Self-induced vomiting UMLS C2242996 Tingling C0042035 Urination disorders HSDN C0018784 Deafness sensorineural C0023521 Globoid cell leukodystrophy OrphaNet C1963184 Nystagmus adverse event C0580190 3-phosphoglycerate dehydrogenase deficiency MalaCards C0948288 Conjunctival discharge C0009763 Conjunctivitis UMLS C0018926 Emesis bloody C0014335 Enteritis HSDN C4084802 Usual severity diarrhea C0472813 X-linked agammaglobulinemia with growth hormone deficiency HPO C0030193 Sense of pain C0040428 Abrasion dental HSDN C4084766 Vomiting C0949570 Allergies wheat HSDN C2242996 Tingling C0003838 Arterial occlusive diseases HSDN C4050613 Anxiety C0012236 Digeorge syndrome MalaCards|HPO C1962972 Proteinuria adverse event C0007820 Cerebrovascular disorders HSDN C3274924 Have been coughing C0004364 Autoimmune diseases HSDN C0575081 Abnormal gait C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0025517 Metabolic diseases HSDN C0034150 Skin purpura C0017178 Gastrointestinal diseases HSDN C0151889 Reflexes tendon increased C1857855 Spastic paraplegia 29, autosomal dominant MalaCards C4084784 Diarrhea C0015663 Fasting HSDN C0042963 Symptoms vomiting C1000483 Genus anemia HSDN C0271215 Blindness legal C1527231 Adrenomyeloneuropathy MalaCards|HPO C0042571 Vertigo subjective C0036095 Salivary gland neoplasms HSDN C0026826 High muscle tone C1846142 Hoyeraal-hreidarsson syndrome OrphaNet|HPO|MalaCards C0020455 Hypergammaglobulinemia C0919267 Ovarian neoplasm HSDN C0013604 Edematous C1457883 Aggressive reaction HSDN C2024878 Cardiovascular surgery result: dyspnea C1962958 Hematoma adverse event HSDN C0004134 Dyssynergia C1846574 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy HPO C4085642 Level of joint stiffness C3809490 Chromosome 3q13.31 deletion syndrome MalaCards C3463815 Feel fatigue C0009319 Colitis HSDN C0241210 Speaking delay C0043379 Xyy karyotype OrphaNet C0039070 Collapse fleeting C0019829 Hodgkin disease HSDN C1279888 Proteinuria of undiagnosed cause C0003838 Arterial occlusive diseases HSDN C0015469 Facial paralysis C0009197 Cochlear diseases HSDN C0042963 Symptoms vomiting C0025149 Medulloblastoma HSDN|UMLS C1963281 Vomiting adverse event C0004352 Autistic disorder HSDN C0034150 Skin purpura C0030328 Panniculitis, nodular nonsuppurative HSDN C1963086 Confusion adverse event C0521542 Brainstem infarct HSDN C0413252 Hypothermia due to exposure C0025063 Mediastinal neoplasms HSDN C0812426 Kidney problem C0403414 Acute post-streptococcal glomerulonephritis UMLS C4084897 Sleep disturbance subordinate domain C0268242 Niemann-pick disease, type a MalaCards C3641755 Have constipation C4041080 Neurocognitive disorders HSDN C4084724 Usual severity constipation C1836704 Arrhythmogenic right ventricular dysplasia, familial, 7 MalaCards C0034150 Skin purpura C0031099 Periodontitis HSDN C0086565 Liver function abnormal C0007095 Carcinoid tumor MalaCards C2203646 Jaundice C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0015230 Exanthem C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0011206 Delirium acute C0042847 Vitamin b 12 deficiency HSDN C1838869 Proximal neurogenic muscle weakness C0085655 Polymyositis OrphaNet|MalaCards C4085210 Usual severity pain C0012644 Animal disease models HSDN C0040485 Wryneck C0032962 Pregnancy complications HSDN C2032396 Pelvic pain on the right C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4085317 Diarrhea frequency C0042133 Uterine fibroids HSDN C4084769 Vomiting frequency C0014849 Esophageal and gastric varices HSDN C1384666 Decreased hearing C0020473 Hyperlipidemia HSDN C2024878 Cardiovascular surgery result: dyspnea C0151744 Myocardial ischemia HSDN C0426579 Anorexia symptom C0013291 Duodenal neoplasms HSDN C0009806 Constipate C1527429 Increased blood npn HSDN C3665386 Abnormal vision C0345407 Osteopetrosis, autosomal recessive 3 HPO C0349506 Sun sensitivity C0751039 Cockayne syndrome, type i HPO C4084775 Usual severity weight loss C0040028 Thrombocythemia, essential MalaCards C0917816 Deficiency mental C2749020 Mental retardation, x linked, znf711 related MalaCards|HPO C4084802 Usual severity diarrhea C0079731 B-cell lymphomas HSDN C2919142 Short stature adverse event C2751297 Sthag6 MalaCards|HPO C2237041 Shox gene with short stature C1970109 Aromatase excess syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C1962974 Chylothorax adverse event HSDN C0011991 Loose stools C0019284 Diaphragmatic hernia HSDN C0018777 Deafness, conductive C1857340 Deafness conductive ptosis skeletal anomalies OrphaNet|MalaCards C0036659 Sensation disorder C4048184 Trochlear nerve diseases HSDN C0027796 Neuralgias C1999266 Depression adverse event HSDN C0423742 Intercourse pain C0242342 Sheehan syndrome OrphaNet|MalaCards C0013362 Dysarthrias C0026654 Moyamoya disease HSDN C0241210 Speaking delay C0015393 Eye abnormalities MalaCards C2203646 Jaundice C0003507 Aortic valve stenosis HSDN C0037317 Sleep disturbance C0268365 Marfanoid hypermobility syndrome MalaCards C0027066 Myoclonic jerking C0007785 Cerebral infarction HSDN C4084788 Have dizziness C0009404 Colorectal neoplasms HSDN C2315100 Pediatric failure to thrive C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C0023530 Leukopenia C3469527 Fanconi anemia complementation group g MalaCards C0015672 Decreased energy C3714644 Thymus neoplasms MalaCards C4084725 Usual severity cough C0006840 Candidiasis HSDN C1999266 Depression adverse event C1858501 Spinocerebellar ataxia 12 MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0021655 Insulin resistance HSDN C0015402 Hemorrhage eye C0019099 Hemorrhagic fever, crimean HSDN C0497247 Blood pressure elevation C1444199 Alkaptonuric ochronosis MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0021053 Immune system diseases HSDN C0023380 Lethargy C0041582 Ulcer HSDN C4084775 Usual severity weight loss C0023364 Leptospirosis HSDN C3887638 Failure to thrive in infant C3658208 Disbioses HSDN C2911645 Weight loss adverse event C0003507 Aortic valve stenosis HSDN C4084784 Diarrhea C0014457 Eosinophilia HSDN C1963170 Hypothermia adverse event C0017636 Glioblastoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017920 Glycogen storage disease type i HSDN C0518090 Frequency of pain question C0080032 Pleural effusion, malignant HSDN C0454644 Delayed language development C1832200 Peroxisome biogenesis disorders HPO C0700078 Deep tendon reflex decrease C0020072 Hereditary sensory autonomic neuropathy, type 2 HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0005119 Bereavement HSDN C0424755 Fever symptoms C3495559 Juvenile arthritis OrphaNet C1963252 Tremor adverse event C0037773 Spastic paraplegia, hereditary HSDN C2911647 Weight gain adverse event C0034067 Pulmonary emphysema HSDN C0460137 Push down or depress C0018523 Hallervorden-spatz syndrome MalaCards|HPO C3898969 Have been vomiting C2931002 Congenital disorder of glycosylation type 1h MalaCards C0007166 Cardiac output decreased C0013927 Embolism, amniotic fluid HSDN C0030554 Abnormal sensation C0040409 Tongue diseases HSDN C0018784 Deafness sensorineural C0037274 Dermatologic disorders HSDN C3463815 Feel fatigue C0268381 Primary amyloidosis OrphaNet|MalaCards C0019079 Bloody sputum C0854973 Stage ii adenosquamous cell carcinoma of lung UMLS C2315100 Pediatric failure to thrive C1864723 Pyridoxamine 5-prime-phosphate oxidase deficiency HPO C0013428 Painful urination C0279682 Bladder adenocarcinoma UMLS C0013604 Edematous C0013377 Dysgerminoma HSDN C0024031 Back pain lower back C0262655 Recurrent urinary tract infection HSDN C1963281 Vomiting adverse event C0032268 Pneumocephalus HSDN C0030232 Color loss C1963107 Euphoria adverse event HSDN C2032396 Pelvic pain on the right C0034888 Rectal prolapse HSDN C0018991 Paralysis one side of body C0018995 Hemochromatosis HSDN C0085636 Light sensitivity C0020678 Hypotrichosis HSDN C0019572 Hairiness C0340834 Hennekam lymphangiectasia lymphedema syndrome HPO C0018772 Deafness C0006012 Borderline personality disorder HSDN C0015970 Fever unknown origin C3463824 Myelodysplastic syndrome HSDN C0221184 Hemianopsia bitemporal C1762616 Meningioma, benign, no icd-o subtype MalaCards C0151825 Ostalgia C2239176 Liver carcinoma MalaCards C0012833 Dizzy C0151467 Addisonian crisis MalaCards C4084802 Usual severity diarrhea C0585442 Osteosarcoma of bone HSDN C0242936 Center pain C0021568 Bites insect stings HSDN C0013604 Edematous C0013473 Eating disorders HSDN C2242996 Tingling C0432240 Stuve-wiedemann dysplasia OrphaNet|HPO C1963281 Vomiting adverse event C0080178 Spina bifida HSDN C0015672 Decreased energy C0002989 Epithelioid hemangioma of skin HSDN C2984058 Have pain C0001824 Agranulocytosis HSDN C4084767 Bothered by vomiting C0034530 Injury radiation HSDN C4084788 Have dizziness C0020456 Hyperglycemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040761 Transposition of great vessels HSDN C4085548 Usual severity dizziness C0517555 Venous thrombosis after immobility HSDN C2029884 Hearing loss by exam C0037313 Sleep HSDN C0162298 Stiffness joints C3711162 Metatropic dysplasia type 1 MalaCards C4085210 Usual severity pain C0007774 Cerebral arterial diseases HSDN C4084724 Usual severity constipation C1836544 Schindler disease, type i MalaCards C2911647 Weight gain adverse event C0007787 Transient ischemic attack HSDN C0085128 Cardiac output elevated C0021818 Intervertebral disk displacement HSDN C0349588 Stature short C0796208 Mental retardation, x-linked 3 HPO C1963252 Tremor adverse event C0041466 Typhoid fever MalaCards C0234146 Absent reflex C1844934 Arthrogryposis multiplex congenita, distal, x-linked HPO C0236000 Jaw bone pain C0085096 Peripheral vascular diseases UMLS C0042963 Symptoms vomiting C0238154 Epidural hematoma HSDN C0413252 Hypothermia due to exposure C0015695 Fatty liver HSDN C2911645 Weight loss adverse event C0005940 Bone diseases HSDN C4085549 Dizziness C0002438 Amebiasis HSDN C0151825 Ostalgia C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0003862 Pain joint C0019080 Hemorrhage HSDN C0018775 Hearing loss bilateral C0024121 Lung neoplasms HSDN C0022107 Fussiness C0393706 Early infantile epileptic encephalopathy with suppression bursts MalaCards C0241210 Speaking delay C0023014 Language development disorders MalaCards C0043094 Weight gain C0428977 Bradycardia HSDN C0027498 Nausea vomiting C3463897 Hydatidiform mole, recurrent, 1 MalaCards C0034933 Abnormal reflexes C0014068 Encephalomalacia HSDN C0018784 Deafness sensorineural C0022660 Kidney failure, acute HSDN C2242579 Lingual dystonia C3554447 Dystonia 25 MalaCards C0149793 Transient monocular blindness C0007787 Transient ischemic attack UMLS C0005745 Blepharoptosis C0079541 Holoprosencephaly MalaCards C0037763 Spasm C3495422 Finding relating to sexuality and sexual activity HSDN C0019209 Large liver C3150926 Anemia, congenital dyserythropoietic, type iv HPO C2237041 Shox gene with short stature C1842465 Lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones OrphaNet|MalaCards C0000727 Abdomen acute C0398625 Protein c deficiency HSDN C1962972 Proteinuria adverse event C0016665 Fracture, nos with nonunion HSDN C0518090 Frequency of pain question C0019310 Hernia, obturator HSDN C0413252 Hypothermia due to exposure C0392622 Toxic effect of carbon tetrachloride HSDN C0007758 Cerebellar ataxia C0029125 Optic atrophies, hereditary HSDN C4084769 Vomiting frequency C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C1860844 Sparse, thin hair C4015495 Cerebellofaciodental syndrome MalaCards C0917816 Deficiency mental C3810363 Bosch-boonstra-schaaf optic atrophy syndrome MalaCards C1963184 Nystagmus adverse event C1862263 Bpes without ovarian failure HPO C0851578 Disorder sleep C0042769 Virus diseases HSDN C1963086 Confusion adverse event C0236969 Substance-related disorders HSDN C1961131 Cough adverse event C0221348 Hereditary lymphedema and yellow nails OrphaNet|MalaCards C0151889 Reflexes tendon increased C1847640 Kufor-rakeb syndrome MalaCards|HPO C0007758 Cerebellar ataxia C0406740 Kohlschutter tonz syndrome MalaCards|HPO C4084724 Usual severity constipation C1845862 Creatine deficiency, x-linked OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0024530 Malaria HSDN C0031911 Pigment deposition C0751676 Basal cell cancer MalaCards C1963184 Nystagmus adverse event C1859194 Griscelli syndrome, type 1 OrphaNet|HPO|MalaCards C4085661 Usual severity nausea C3714644 Thymus neoplasms HSDN C0424790 Chill shaking C0030636 Pasteurella infection DiseaseOntology|MalaCards C4084775 Usual severity weight loss C1546847 Entity name part type - family HSDN C0037316 Not enough sleeping C0014550 Epilepsies, myoclonic HSDN C0036572 Convulsion C0340803 Capillary malformation (disorder) HSDN C1971624 Appetite absent C0005967 Bone neoplasms HSDN C1963252 Tremor adverse event C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C1963247 Ventricular tachycardia adverse event C0340485 Familial ventricular tachycardia MalaCards C0036572 Convulsion C1332961 Childhood cerebral diffuse astrocytoma UMLS C0013604 Edematous C0030583 Parotitis HSDN C0237326 Defecation pain C3683846 Chromosome 17p deletion syndrome MalaCards C0019572 Hairiness C0004936 Mental disorders HSDN C0749858 Upper extremity weakness unilateral C0741096 Upper_ext problem UMLS C0019209 Large liver C2677590 Congenital disorder of glycosylation, type in OrphaNet|HPO|MalaCards C2126234 Urinary incontinence before reaching bathroom C0042024 Urinary incontinence UMLS C0151825 Ostalgia C1848336 Dent disease 1 HPO|UMLS C0013362 Dysarthrias C0014548 Epilepsy, generalized HSDN C0027066 Myoclonic jerking C0598392 Lennox syndrome MalaCards C1963091 Diarrhea adverse event C2062326 Eosinophilic enteropathy OrphaNet|MalaCards C0007758 Cerebellar ataxia C0007873 Uterine cervical neoplasm HSDN C0002170 Alopecia disorders C1704421 Skin pigmentation disorder MalaCards C3887784 Decreased urine output C0011175 Dehydration HSDN C0151786 Weakness muscle C0021400 Influenza HSDN C4085862 Bothered by nausea C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0040485 Wryneck C0080178 Spina bifida HSDN C0000737 Abdomen pain C0149721 Left ventricular hypertrophy HSDN C4085862 Bothered by nausea C0007099 Carcinoma in situ HSDN C1999266 Depression adverse event C0017205 Gaucher disease OrphaNet|MalaCards C0032617 High urine output C0042029 Urinary tract infection HSDN C3815497 Cough C3495559 Juvenile arthritis HSDN C0020580 Decreased sensation C0005695 Bladder neoplasm HSDN C0018681 Headache, cephalalgia C0010276 Craniopharyngioma OrphaNet|HPO|MalaCards C3898969 Have been vomiting C0268242 Niemann-pick disease, type a MalaCards|HPO C0036572 Convulsion C3151056 Spastic paraplegia 51, autosomal recessive MalaCards|HPO|UMLS C0009421 Comatose C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C2984058 Have pain C0042974 Von willebrand disease HSDN C1557397 Adverse event associated with pain C0038463 Strongyloides infection HSDN C4085317 Diarrhea frequency C0149573 Structure of posterior inferior cerebellar artery HSDN C0518090 Frequency of pain question C0024636 Malocclusion HSDN C0018772 Deafness C0038013 Ankylosing spondylitis HSDN C0042963 Symptoms vomiting C0016057 Fibrosarcoma HSDN C0026821 Cramp C0021818 Intervertebral disk displacement HSDN C4085661 Usual severity nausea C0002989 Epithelioid hemangioma of skin HSDN C0036572 Convulsion C0032969 Pregnancy in diabetics HSDN C4085210 Usual severity pain C0005745 Blepharoptosis HSDN C4084767 Bothered by vomiting C0029835 Other specified tularemia nos DiseaseOntology|MalaCards C0034933 Abnormal reflexes C1963137 Hydrocephalus adverse event HSDN C2700617 Irritation - emotion C1847987 Huntington disease-like 2 MalaCards|HPO C0017672 Pain tongue C0024409 Machiavellianism HSDN C0013404 Respiratory difficulty C0005891 Bodies image HSDN C1962972 Proteinuria adverse event C0003864 Arthritis HSDN C1565249 Limitation, mobility C0023890 Liver cirrhosis HSDN C4084802 Usual severity diarrhea C3827868 Tachycardia by ecg finding HSDN C0035078 Failure kidney C2931187 Nephropathic cystinosis MalaCards C0007758 Cerebellar ataxia C2931355 Spastic paraplegia 3, autosomal dominant OrphaNet|MalaCards C0019079 Bloody sputum C0010356 Cross infection HSDN C4084774 Have weight loss C0006107 Concussion HSDN C3815497 Cough C0867389 Chronic graft-versus-host disease MalaCards C0036572 Convulsion C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) MalaCards|UMLS C0851578 Disorder sleep C0950123 Inborn genetic disease HSDN C0518090 Frequency of pain question C0013369 Dysentery HSDN C0018681 Headache, cephalalgia C1260386 Glucocorticoid-remediable aldosteronism HPO C1565249 Limitation, mobility C0016542 Foreign body HSDN C0019572 Hairiness C1860215 Acanthosis nigricans with muscle cramps and acral enlargement MalaCards C1546759 Specimen source codes - pustule C0085435 Arthritis, reactive OrphaNet|MalaCards C0747556 Pharyngitis recurrent C0398621 Hypoplasminogenemia MalaCards C4084769 Vomiting frequency C0949570 Allergies wheat HSDN C3898969 Have been vomiting C0030305 Pancreatitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2911243 Encounter due to family history of colonic polyps HSDN C0023380 Lethargy C0014055 Encephalitis, epidemic HSDN C0406407 Cholinergic pruritus C0042109 Urticaria UMLS C0015672 Decreased energy C0600519 Ventricular remodeling HSDN C0349489 Fetal hypoxia C2909036 Twin twin transfusion HSDN C3178766 Nociceptive pain C0006430 Burning mouth syndrome HSDN C0036572 Convulsion C0278186 Atonic seizure, long UMLS C2911647 Weight gain adverse event C0010692 Cystitis HSDN C0917816 Deficiency mental C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C0151786 Weakness muscle C2748910 Rett syndrome, atypical MalaCards C0009080 Finger clubbing C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C1963063 Anorexia adverse event C0031090 Periodontal diseases HSDN C0013404 Respiratory difficulty C0854980 Stage ii large cell carcinoma of lung UMLS C4084776 Weight loss C0011875 Diabetic angiopathies HSDN C1963071 Back pain adverse event C0004238 Atrial fibrillation HSDN C0413252 Hypothermia due to exposure C0032344 Poisoning aspects HSDN C2220008 Baby moving in uterus C0235659 Reduced fetal movement UMLS C0026858 Musculoskeletal pain C0576093 Knee joint valgus deformity HSDN C4085211 Pain distress question C0014055 Encephalitis, epidemic HSDN C4084774 Have weight loss C0334419 Pheochromocytoma, malignant MalaCards C4085317 Diarrhea frequency C0524910 Hepatitis c, chronic HSDN C3815497 Cough C0041316 Lymph node tuberculosis DiseaseOntology|MalaCards C0000737 Abdomen pain C0238909 Cat scratch MalaCards C0019209 Large liver C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0016079 Figural aftereffects HSDN C0033377 Caudal displacement C1855722 Iris coloboma with ptosis, hypertelorism, and mental retardation MalaCards|HPO C0013404 Respiratory difficulty C0032269 Pneumococcal infections HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0037199 Sinusitis HSDN C3665492 Pigmentations C1838702 Retinitis pigmentosa 13 MalaCards C0037199 Sinus infection C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0020305 Fetal edema C0024248 Cyst lymph HSDN C1999266 Depression adverse event C0162531 Hereditary coproporphyria OrphaNet|HPO C0015468 Face pain C0029182 Orbit (eye disorders) HSDN C2911647 Weight gain adverse event C1962979 Burn adverse event HSDN C1549543 Administration method - pain C0028960 Oligospermia HSDN C0043094 Weight gain C0019080 Hemorrhage HSDN C1549543 Administration method - pain C0018021 Goiter HSDN C1838579 Pseudobulbar signs C2752008 Spastic paraplegia-50, autosomal recessive MalaCards|HPO|UMLS C0344306 Intercostal neuralgia C0393897 Intercostal neuropathy UMLS C4084802 Usual severity diarrhea C0033700 Infection proteus HSDN C0020505 Excessive eating C2984299 Asthma pathway HSDN C0007166 Cardiac output decreased C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0557874 Global developmental delay C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C0034150 Skin purpura C1269683 Major depressive disorder HSDN C0042798 Vision dim C1956390 Cranial arteritis MalaCards C4084723 Constipation C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0522224 Palsied C0037944 Spinal stenosis HSDN C0018681 Headache, cephalalgia C0280383 Lymphoepithelioma of the nasopharynx, stage iii UMLS C3887638 Failure to thrive in infant C0432283 Osteoglophonic dwarfism MalaCards|HPO C0030794 Pelvis pain C3178770 Nutcracker syndrome, renal HSDN C0332573 Macula C1868311 Piebald trait neurologic defects OrphaNet|MalaCards C0002962 Angina C0042131 Uterine diseases HSDN C4085317 Diarrhea frequency C1443901 Intestinal botulism OrphaNet|MalaCards C0036572 Convulsion C0042974 Von willebrand disease HSDN C4084726 Distress cough C0026896 Myasthenia gravis HSDN C0349588 Stature short C3714043 Trisomy xq28 OrphaNet|HPO C3898969 Have been vomiting C0035956 Rupture spontaneous HSDN C0036572 Convulsion C3280240 Microcephaly, epilepsy, and diabetes syndrome MalaCards|UMLS C0009806 Constipate C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C1963087 Constipation adverse event C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C1704421 Skin pigmentation disorder HSDN C0028962 Oliguria and anuria nos C0028961 Oliguria UMLS C0002965 Crescendo angina C0342649 Vascular calcification HSDN C1962972 Proteinuria adverse event C0004623 Bacterial infections HSDN C3641756 Have diarrhea C0016667 Fragile x syndrome HSDN C0232466 Feeding difficulty C3281234 Combined oxidative phosphorylation deficiency 9 MalaCards C0020455 Hypergammaglobulinemia C0079335 Aids feline HSDN C0008031 Pain chest C3203102 Idiopathic pulmonary arterial hypertension OrphaNet C1384666 Decreased hearing C0700208 Acquired scoliosis HSDN C4020887 Photodysphoria C0013575 Ectodermal dysplasia MalaCards C0023015 Language handicap C1322286 Thymoma, type c MalaCards C0004134 Dyssynergia C0017168 Gastroesophageal reflux disease HSDN C4084776 Weight loss C0035579 Rickets HSDN C0002622 Amnesias C0002895 Anemia, sickle cell HSDN C0151908 Dry skin C1969056 Leopard syndrome 2 MalaCards|HPO C0019521 Hiccoughs C0153414 Malignant neoplasm of middle third of esophagus MalaCards C3274924 Have been coughing C0546837 Malignant neoplasm of esophagus OrphaNet|MalaCards C0030193 Sense of pain C3273216 Invasive lobular breast carcinoma, pleomorphic variant UMLS C0043094 Weight gain C1568272 Tendinopathy HSDN C0030193 Sense of pain C0011603 Dermatitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C4084723 Constipation C1261473 Sarcoma HSDN C0011991 Loose stools C0037650 Somatoform disorder HSDN C1961131 Cough adverse event C0340848 Pulmonary venoocclusive disease 2, autosomal recessive HPO C1145670 Failure respiratory C0001193 Apert syndrome MalaCards|HPO C0013404 Respiratory difficulty C1548578 Location characteristic id - smoking HSDN C0034150 Skin purpura C2936664 Acquired hypogammaglobulinemia MalaCards C0020673 Hypothermia (central) (local) C0019159 Hepatitis a HSDN C0018772 Deafness C0016395 Focal dermal hypoplasia OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0022593 Keratosis HSDN C0015672 Decreased energy C0029443 Osteomyelitis HSDN C0038002 Spleen enlargement C1861455 Stomatocytosis i HPO C0009792 Consciousness disorder C0011303 Demyelinating diseases HSDN C0241165 Skin thickening C2676191 Pituitary adenoma, familial isolated (disorder) MalaCards C3539891 Pelvic pain to the rear C0021359 Infertility HSDN C0018777 Deafness, conductive C1849661 Acrootoocular syndrome MalaCards C0700590 Diaphoresis excessive C0032533 Polymyalgia rheumatica MalaCards C0424755 Fever symptoms C0040137 Thyroid nodule HSDN C0036659 Sensation disorder C0154743 Neuropathy ulnar HSDN C1963091 Diarrhea adverse event C0031542 Phlebitis HSDN C0242936 Center pain C0026771 Trauma multiple HSDN C1963137 Hydrocephalus adverse event C4015710 Tenorio syndrome MalaCards C0002965 Crescendo angina C0040046 Thrombophlebitis HSDN C0007758 Cerebellar ataxia C0001973 Alcoholic intoxication, chronic HSDN|UMLS C0242936 Center pain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0019079 Bloody sputum C0854979 Stage i large cell carcinoma of lung UMLS C0015970 Fever unknown origin C0085437 Meningitis, bacterial HSDN C0424755 Fever symptoms C3714509 Nutrition disorders HSDN C1279888 Proteinuria of undiagnosed cause C1845285 Martin-probst deafness-mental retardation syndrome MalaCards C0242936 Center pain C0007274 Carotid artery thrombosis HSDN C1963180 Neck pain adverse event C0178842 Sensory feedback HSDN C2315100 Pediatric failure to thrive C0002395 Alzheimer's disease HSDN C0013362 Dysarthrias C0022758 Kap HSDN C2984058 Have pain C1258215 Ileus HSDN C0031911 Pigment deposition C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C1384666 Decreased hearing C1961835 Gaucher disease, type 1 MalaCards C2032396 Pelvic pain on the right C0023903 Liver neoplasms HSDN C0015468 Face pain C0019364 Herpes zoster ophthalmicus HSDN C0034933 Abnormal reflexes C0037286 Skin neoplasms HSDN C1962972 Proteinuria adverse event C0035436 Rheumatic fever HSDN C2984058 Have pain C0010417 Cryptorchidism HSDN C0036572 Convulsion C3152055 D-2-hydroxyglutaric aciduria 1 HPO|UMLS C0012833 Dizzy C0035334 Retinitis pigmentosa HSDN C0038002 Spleen enlargement C2931347 Cardiac form of generalized glycogenosis MalaCards|HPO C0019209 Large liver C0035921 Congenital rubella syndrome OrphaNet|MalaCards C0003862 Pain joint C0034362 Q fever DiseaseOntology|MalaCards C2911647 Weight gain adverse event C0086543 Cataract nos HSDN C0013404 Respiratory difficulty C1862939 Amyotrophic lateral sclerosis 1 MalaCards C4084726 Distress cough C0027686 Pathologic neovascularization HSDN C0518090 Frequency of pain question C0206239 Cubital syndrome tunnel HSDN C2024893 Cardiovascular surgery result: fatigue C0019621 Histiocytosis, langerhans-cell HSDN C2242996 Tingling C0262655 Recurrent urinary tract infection HSDN C0000727 Abdomen acute C0242698 Ventricular dysfunction, left HSDN C0013362 Dysarthrias C3809824 Parkinson disease 20, early-onset MalaCards C4085549 Dizziness C0152054 Therapeutic touch HSDN C0015672 Decreased energy C0162872 Aortic aneurysm, thoracic HSDN C0018834 Brash C0795907 Conotruncal anomaly face syndrome MalaCards|HPO C2242996 Tingling C1458155 Mammary neoplasms HSDN C2984058 Have pain C0002986 Fabry disease HSDN C4084776 Weight loss C0021361 Female infertility HSDN C2919142 Short stature adverse event C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C4085210 Usual severity pain C0035086 Renal osteodystrophy HSDN C0242670 Chronic vegetative state C0020538 Hypertensive disease HSDN C0344315 Mood depressed C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C4084776 Weight loss C0009759 Conjunctival diseases HSDN C0206146 Myocardial stunning C0013806 Electroplexy shock therapy HSDN C1384666 Decreased hearing C1859569 Bardet-biedl syndrome 11 HPO C0242936 Center pain C0016995 Gambling HSDN C0018524 Hallucinate C1090821 Sepsis (invertebrate) HSDN C0241210 Speaking delay C2674937 Chromosome 10q26 deletion syndrome MalaCards C1963184 Nystagmus adverse event C0795950 Corpus callosum agenesis neuronopathy MalaCards|HPO C2032396 Pelvic pain on the right C0206687 Carcinoma, endometrioid HSDN C4085210 Usual severity pain C0041330 Tuberculosis, spinal HSDN C0018772 Deafness C0036202 Sarcoidosis HSDN C0002963 Angina variant C0014852 Esophageal diseases HSDN C4085548 Usual severity dizziness C0453996 Tobacco smoking HSDN C1961131 Cough adverse event C0017601 Glaucomas HSDN C4084768 Usual severity vomiting C0031117 Peripheral neuropathy HSDN C2242996 Tingling C0085084 Motor neuron disease HSDN C4084768 Usual severity vomiting C3814778 Hemolytic index HSDN C4084766 Vomiting C0016751 Hereditary fructose intolerance syndrome HSDN|HPO C4085317 Diarrhea frequency C0162534 Prion diseases HSDN C3463815 Feel fatigue C0027439 Nasopharyngeal neoplasms HSDN C0015672 Decreased energy C0042164 Uveitis HSDN C0878638 Tongue signs C0043459 Zellweger syndrome MalaCards|HPO C1384666 Decreased hearing C0009241 Cognition disorders HSDN C0522224 Palsied C0032285 Pneumonia HSDN C0518090 Frequency of pain question C0276275 Disease due to parvoviridae HSDN C0242936 Center pain C0003486 Aortic aneurysm HSDN C0027497 Queasy C0013595 Eczema HSDN C0033377 Caudal displacement C1834558 Myopathy, centronuclear, autosomal dominant HPO C0034933 Abnormal reflexes C0037930 Spinal cord neoplasms HSDN C1999266 Depression adverse event C1439329 Cbs gene HPO C0018681 Headache, cephalalgia C0028850 Ocular motility disorders HSDN C4085317 Diarrhea frequency C1848590 Vascular hyalinosis MalaCards C0575081 Abnormal gait C3889636 Spinocerebellar ataxia 37 MalaCards C0231835 Respiration rate increased C1761609 Aspiration pneumonitis MalaCards C0041657 Consciousness loss C0024630 Malingering HSDN C0042963 Symptoms vomiting C0024530 Malaria HSDN C4084723 Constipation C0518450 Spinal fractures HSDN C3814530 Skin vesicle C0268374 Adult junctional epidermolysis bullosa (disorder) OrphaNet|MalaCards C3539890 Pelvic pain causes awakening at night C0026769 Multiple sclerosis HSDN C0010200 Cough symptom C1707407 Clear cell carcinoma of lung, large cell type UMLS C1557397 Adverse event associated with pain C0001618 Tumors of adrenal cortex HSDN C0009421 Comatose C0751278 Metachromatic leukodystrophy, infant MalaCards C1963184 Nystagmus adverse event C3809007 Cardiofaciocutaneous syndrome 4 MalaCards C0454644 Delayed language development C0268228 Neuraminidase 1 deficiency OrphaNet C0150055 Pain chronic C0035258 Restless legs syndrome HSDN C0393766 Postviral excessive daytime sleepiness C1285427 Sequelae of disorders classified by disorder-system UMLS C0018681 Headache, cephalalgia C0043124 West nile fever MalaCards C0013421 Dystonia C0006434 Burn injury HSDN C0015672 Decreased energy C0026272 Mixed connective tissue disease OrphaNet|MalaCards C0000727 Abdomen acute C0030330 Panniculitis, peritoneal HSDN C0013390 Cramps menstrual C0007222 Cardiovascular diseases HSDN C4084897 Sleep disturbance subordinate domain C2748910 Rett syndrome, atypical MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0021308 Infarction HSDN C0033774 Skin pruritus C0030920 Peptic ulcer HSDN C0033774 Skin pruritus C0002736 Amyotrophic lateral sclerosis HSDN C0917816 Deficiency mental C0432243 Spondyloepimetaphyseal dysplasia with joint laxity HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0031030 Periapical periodontitis HSDN C0241210 Speaking delay C1845539 Autism, x-linked, susceptibility to, 2 (finding) HPO C0015230 Exanthem C1142528 Exanthema facial UMLS C0024312 Lymphocytopenia C1969799 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation MalaCards C0018808 Murmur C1414899 Gaa gene HSDN C0085631 Abnormal excitement C0032962 Pregnancy complications HSDN C3274924 Have been coughing C0016627 Avian influenza DiseaseOntology|MalaCards C1557397 Adverse event associated with pain C0009186 Coccidioidomycosis HSDN C3887638 Failure to thrive in infant C0268250 Gaucher disease, type 2 (disorder) MalaCards|HPO C0033377 Caudal displacement C1853949 Myasthenia, familial infantile, 1 MalaCards|HPO C0004134 Dyssynergia C0751882 Myasthenic syndromes, congenital HSDN C3641756 Have diarrhea C0010631 Cystadenocarcinoma HSDN C0011991 Loose stools C1266015 Delta cell carcinoma UMLS C0012569 Double vision C0314657 Genetic predisposition HSDN C4085549 Dizziness C0079731 B-cell lymphomas HSDN C0427055 Face weakness C1864668 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4 MalaCards|HPO|UMLS C0151889 Reflexes tendon increased C2931821 Nakamura osame syndrome MalaCards|HPO C0242936 Center pain C0034194 Pyloric stenosis HSDN C2911645 Weight loss adverse event C0520946 Emotional hypersensitivity HSDN C0000737 Abdomen pain C0030567 Parkinson disease HSDN C0018777 Deafness, conductive C2020284 Stickler syndrome, type 1 MalaCards C4085549 Dizziness C0016053 Fibromyalgia HSDN C0030552 Paralysis partial C0035920 Rubella HSDN C0013604 Edematous C0038016 Spondylolisthesis HSDN C1963087 Constipation adverse event C0000771 Abnormalities, drug induced HSDN C1963281 Vomiting adverse event C1135841 Zoster sine eruptione HSDN C1384666 Decreased hearing C0023931 Lobstein's disease HPO C0042963 Symptoms vomiting C0376532 Epilepsy, rolandic HSDN C3146279 Coma C0005591 Avian disease HSDN C0404561 Menopausal concentration lack C0404559 Perimenopausal disorder UMLS C0009806 Constipate C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0518090 Frequency of pain question C0020877 Ileitis HSDN C0027497 Queasy C0034065 Pulmonary embolism HSDN|UMLS C2984057 Have nausea C0035309 Retinal diseases HSDN C4084769 Vomiting frequency C0236969 Substance-related disorders HSDN C1579931 Depressed - symptom C3554605 Mc3dn2 MalaCards C1549543 Administration method - pain C0015670 Child father HSDN C4084766 Vomiting C0030305 Pancreatitis HSDN C1069915 Vertigo C0206504 Tympanic membrane perforation HSDN C0042571 Vertigo subjective C0038454 Cerebrovascular accident HSDN C0030486 Extremity paralysis, lower C0013364 Dysautonomia, familial HSDN C0035229 Respiratory function impaired C1836327 Rhabdoid tumor predisposition syndrome 1 (disorder) MalaCards C0424790 Chill shaking C0243026 Sepsis UMLS C0041834 Erythematous condition C0038325 Stevens-johnson syndrome OrphaNet|HPO C4085210 Usual severity pain C0016995 Gambling HSDN C0557874 Global developmental delay C2674173 Achondroplasia, severe, with developmental delay and acanthosis nigricans HPO C0848203 Male pelvic pain C1261473 Sarcoma HSDN C0237326 Defecation pain C0014805 Primary erythermalgia MalaCards|HPO C0557874 Global developmental delay C1859359 Camptodactyly syndrome, guadalajara type i OrphaNet|MalaCards C0034151 Hyperglobulinemic purpura C0020639 Hypoproteinemia HSDN C0018784 Deafness sensorineural C0079731 B-cell lymphomas HSDN C0011991 Loose stools C1963266 Uveitis adverse event HSDN C0040264 Ear ringing sound C0020538 Hypertensive disease HSDN C0024032 Birth weight subnormal C0796021 Lowry wood syndrome MalaCards C0085606 Urination urgency C3160718 Parkinson disease, late-onset MalaCards|HPO C0003862 Pain joint C0018199 Granuloma, plasma cell HSDN C0036572 Convulsion C0035579 Rickets HSDN C0011991 Loose stools C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0018834 Brash C0016667 Fragile x syndrome OrphaNet|HPO|MalaCards C0009421 Comatose C0749098 Hematoma, subdural, acute HSDN C0424755 Fever symptoms C1510412 Pseudoaneurysm HSDN C0030193 Sense of pain C0025268 Multiple endocrine neoplasia type 2a HSDN C0020673 Hypothermia (central) (local) C3489413 Lipomatosis, multiple HSDN C0557874 Global developmental delay C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards|HPO C0037384 Snore C1579931 Depressed - symptom HSDN C1069915 Vertigo C0152181 Hypoglossal nerve disease or syndrome HSDN C0036572 Convulsion C2609414 Acute kidney injury HSDN C0007398 Catatonic C0011265 Presenile dementia HSDN C0025287 Meningitis-like C0025295 Meningitis, pneumococcal HSDN C0020580 Decreased sensation C0919267 Ovarian neoplasm HSDN C0018991 Paralysis one side of body C0079744 Diffuse large b-cell lymphoma HSDN C1963065 Apnea adverse event C3539760 Mok wt allele HSDN C0018772 Deafness C1527298 Dysentery, bacillary HSDN C3496180 Sleep apnea C0080040 Polio post syndrome DiseaseOntology|MalaCards C3274924 Have been coughing C0032963 Pregnancy complications, cardiovascular HSDN C0041657 Consciousness loss C3244301 Coverage level - family HSDN C0242936 Center pain C0002448 Ameloblastoma HSDN C2984058 Have pain C0031030 Periapical periodontitis HSDN C0011570 Monopolar depression C2931082 Familial apoceruloplasmin deficiency MalaCards C0030193 Sense of pain C0032533 Polymyalgia rheumatica HSDN|UMLS C0033377 Caudal displacement C3146244 Alcohol related birth defect OrphaNet|MalaCards C4084769 Vomiting frequency C0003850 Arteriosclerosis HSDN C0002962 Angina C0038525 Subarachnoid hemorrhage HSDN C0518090 Frequency of pain question C0016989 Galvanic skin response HSDN C0009421 Comatose C0013080 Down syndrome HSDN C0019209 Large liver C3281234 Combined oxidative phosphorylation deficiency 9 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0085395 Ureaplasma infections HSDN C0030552 Paralysis partial C0238386 Cronkhite-canada disease MalaCards C0042798 Vision dim C0016952 Galactosemias MalaCards C3665492 Pigmentations C0023269 Leiomyosarcoma MalaCards C4085211 Pain distress question C0024810 Marijuana smoking HSDN C3898969 Have been vomiting C0008625 Chromosome aberrations HSDN C4085211 Pain distress question C0264134 Hallux limitus HSDN C0149840 Senile tremor C0392702 Abnormal involuntary movement UMLS C1963137 Hydrocephalus adverse event C0333693 Triploidy syndrome MalaCards C0013362 Dysarthrias C0030567 Parkinson disease MalaCards C0917816 Deficiency mental C1970140 Aplasia cutis congenita, congenital heart defect, and frontonasal cysts HPO C0007758 Cerebellar ataxia C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards C3829611 Nausea frequency C3150933 Hyperaldosteronism, familial, type iii MalaCards C0018772 Deafness C0920350 Autoimmune thyroiditis HSDN C0312416 Morning sickness C0236969 Substance-related disorders HSDN C0039870 Leanness C0020936 Imitative behaviors HSDN C0000737 Abdomen pain C3273034 Moderately differentiated hepatocellular carcinoma UMLS C0004134 Dyssynergia C0027947 Neutropenia HSDN C0018681 Headache, cephalalgia C0023448 Lymphoid leukemia HSDN C0020673 Hypothermia (central) (local) C0022661 Kidney failure, chronic HSDN C1961131 Cough adverse event C3495801 Granulomatosis with polyangiitis OrphaNet|HSDN|HPO|MalaCards C2029884 Hearing loss by exam C0015934 Fetal growth retardation HSDN C0020578 Hyperventilate C0020550 Hyperthyroidism HSDN C0002965 Crescendo angina C0004153 Atherosclerosis HSDN C3463815 Feel fatigue C0043253 Trauma blunt HSDN C0018784 Deafness sensorineural C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4084723 Constipation C0006145 Breast diseases HSDN C0039870 Leanness C0020456 Hyperglycemia HSDN C0015672 Decreased energy C1333045 Cmml with eosinophilia UMLS C0557874 Global developmental delay C1833835 Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency MalaCards C0014591 Bleeding nose C0039483 Giant cell arteritis MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0152018 Esophageal carcinoma OrphaNet|MalaCards C0151786 Weakness muscle C3150786 Muscular dystrophy, limb-girdle, type 1h MalaCards C0522224 Palsied C1556682 Adverse event associated with infection HSDN C0030554 Abnormal sensation C0997768 Glaucoma HSDN C3541349 Syncope C0019699 Hiv seropositivity HSDN C4084773 Bothered by weight gain C0020522 Delayed hypersensitivity HSDN C0162834 Hyperpigmentation C0220766 Congenital hypoplasia of adrenal gland HPO C2220048 Bilateral knee joint pain C3862611 Patellofemoral syndrome of bilateral knees UMLS C0240715 Perineal lump C0153602 Malignant tumor of epididymis UMLS C0043094 Weight gain C0585442 Osteosarcoma of bone HSDN C0018834 Brash C0018801 Heart failure HSDN C0851578 Disorder sleep C3888013 Hypnoses HSDN C0013456 Pain ear C0040435 Tooth diseases HSDN C4085317 Diarrhea frequency C0020676 Hypothyroidism HSDN C0848203 Male pelvic pain C0205788 Histiocytoid hemangioma HSDN C0013404 Respiratory difficulty C0016658 Fracture bone HSDN C0424755 Fever symptoms C0012813 Diverticulitis HSDN C0030193 Sense of pain C0021125 Impulsive behavior HSDN C0042571 Vertigo subjective C3163620 Hypotension adverse event HSDN C0030193 Sense of pain C3808991 Congenital disorder of deglycosylation MalaCards C4084784 Diarrhea C0347555 Friction blister HSDN C4084724 Usual severity constipation C0039231 Tachycardia HSDN C0025222 Black stool C0042470 Guanarito haemorrhagic fever MalaCards C4084723 Constipation C0919267 Ovarian neoplasm HSDN C0038002 Spleen enlargement C1850510 Sialidosis, type i OrphaNet|HPO C0085606 Urination urgency C3711370 Spastic paraplegia type 7 MalaCards C4084776 Weight loss C0751552 Malignant neoplasm of thymus MalaCards C0013604 Edematous C0036457 Scrapie HSDN C4084726 Distress cough C0220847 C hepatitis virus HSDN C0016199 Pain flank C1513719 Mucinous tubular and spindle cell carcinoma of the kidney UMLS C0332606 Facies elfin C0265344 Donohue syndrome HPO|UMLS C4050613 Anxiety C0796237 Mental retardation, x-linked 30 HPO C0427068 Legs weakness C1834235 Neurofibromatosis, familial spinal MalaCards|HPO C0033790 Pseudobulbar palsy C0085278 Antiphospholipid syndrome HSDN C0020538 Hbp C2936861 Cortisol 11-beta-ketoreductase deficiency MalaCards C3829611 Nausea frequency C0014544 Epilepsy HSDN C0030193 Sense of pain C0003950 Ascariasis HSDN C0018926 Emesis bloody C0221773 Hyperamylasemia HSDN C0010200 Cough symptom C0040583 Tracheal stenosis HSDN C4084723 Constipation C0009324 Ulcerative colitis HSDN C1963170 Hypothermia adverse event C2711227 Steatohepatitis HSDN C0009763 Conjunctiva inflammation C1968804 Plasminogen deficiency, type i MalaCards|HPO C0015468 Face pain C3714535 Malocclusion, angle class ii HSDN C3641756 Have diarrhea C0043395 Yellow fever OrphaNet|MalaCards C2029884 Hearing loss by exam C0006277 Bronchitis HSDN C0751837 Gait ataxic C0752160 Hemangioma, cavernous, central nervous system HSDN C4084723 Constipation C2931518 Plexosarcoma MalaCards C4085317 Diarrhea frequency C0027662 Multiple endocrine neoplasia HSDN C0043094 Weight gain C0702094 Agranulocytosis lab result HSDN C4042891 Sleep wake disorders C0001889 Akinetic mutism HSDN C0036572 Convulsion C0030977 Perceptual masking HSDN C0424755 Fever symptoms C1720965 Ectodermal dysplasia 3, anhidrotic HSDN C0042025 Urinary incontinence stress C0022665 Kidney neoplasm HSDN C2024878 Cardiovascular surgery result: dyspnea C0017563 Gingival diseases HSDN C0026838 Spasticity muscle C0997768 Glaucoma HSDN C0040264 Ear ringing sound C0458220 Nervus intermedius neuralgia MalaCards C0024031 Back pain lower back C0850803 Anaphylaxis (non medication) HSDN C0036572 Convulsion C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO|UMLS C2024893 Cardiovascular surgery result: fatigue C0014849 Esophageal and gastric varices HSDN C1557397 Adverse event associated with pain C0014347 Enterobacteriaceae infections HSDN C2984058 Have pain C0035258 Restless legs syndrome HSDN C0020673 Hypothermia (central) (local) C1956346 Coronary artery disease HSDN C4085222 Nausea C0040046 Thrombophlebitis HSDN C0030554 Abnormal sensation C0019625 Sinus histiocytosis MalaCards C3815497 Cough C0016627 Avian influenza DiseaseOntology|MalaCards C0018808 Murmur C0265428 9p+ syndrome MalaCards C0424755 Fever symptoms C0002950 Aneurysms inflammatory HSDN C2984058 Have pain C0030482 Paraepithymia HSDN C0497406 Over weight C0062527 Hepatitis b vaccine HSDN C0004134 Dyssynergia C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0012833 Dizzy C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards C4084724 Usual severity constipation C0034530 Injury radiation HSDN C0270777 Cord edema spinal C0474993 Edema of lumbar cord UMLS C2984057 Have nausea C0042594 Vestibular diseases HSDN C1963184 Nystagmus adverse event C0022283 Incontinentia pigmenti achromians MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0022661 Kidney failure, chronic HSDN C0018772 Deafness C4049994 Insulin resistance measurement HSDN C1963184 Nystagmus adverse event C0338488 Alternating hemiplegia of childhood HPO C0030552 Paralysis partial C1306577 Dies patient HSDN C0020578 Hyperventilate C0282333 Relaxation therapies HSDN C0027497 Queasy C1333307 Adenocarcinoma of distal 1/3 of common bile duct UMLS C0413252 Hypothermia due to exposure C1963137 Hydrocephalus adverse event HSDN C1279888 Proteinuria of undiagnosed cause C0002940 Aneurysm HSDN C0011991 Loose stools C0854795 Resectable hepatic malignant neoplasm MalaCards C0332606 Facies elfin C0268080 Hypercalcemia, idiopathic, of infancy HPO C0575081 Abnormal gait C2931125 Feigenbaum bergeron richardson syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0020461 Hyperkalemia HSDN C0013362 Dysarthrias C0027743 Nerve compression syndrome HSDN C0030552 Paralysis partial C2986717 Anti-n-methyl-d-aspartate receptor encephalitis HSDN C0018772 Deafness C3281297 Deafness, autosomal dominant 4b MalaCards C2024893 Cardiovascular surgery result: fatigue C1532253 Sedentary lifestyle HSDN C0040264 Ear ringing sound C0003873 Rheumatoid arthritis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0242770 Bronchiolitis obliterans organizing pneumonia HSDN C0018775 Hearing loss bilateral C0037286 Skin neoplasms HSDN C3815497 Cough C0162316 Iron deficiency anemia HSDN C1963091 Diarrhea adverse event C0241802 Arthritis, venereal MalaCards C3815497 Cough C0035066 Renal artery obstruction HSDN C0012569 Double vision C0919267 Ovarian neoplasm HSDN C3829611 Nausea frequency C0001883 Airway obstruction HSDN C2919142 Short stature adverse event C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C3898969 Have been vomiting C0035309 Retinal diseases HSDN C0012833 Dizzy C0079731 B-cell lymphomas HSDN C0037384 Snore C0243057 Stomatognathic system abnormalities MalaCards C0917816 Deficiency mental C0035372 Rett syndrome MalaCards C0039070 Collapse fleeting C0270857 Epilepsy, reflex HSDN C3539896 Pelvic pain occurs with urination C0409354 Flexion contracture of hip HSDN C2984058 Have pain C0233629 Thinking and speaking disturbances HSDN C2911645 Weight loss adverse event C0524801 Retinal neoplasms HSDN C3898969 Have been vomiting C0001580 Adolescent behavior HSDN C4084725 Usual severity cough C1955864 Cardiac sinus arrest HSDN C1961131 Cough adverse event C0007621 Neoplastic cell transformation HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1269683 Major depressive disorder HSDN C3665492 Pigmentations C0751434 Classical phenylketonuria MalaCards C0018784 Deafness sensorineural C2673759 Deafness, autosomal recessive 1a (disorder) MalaCards|HPO C0013132 Drooling C3150705 Foxg1 syndrome HPO C0424755 Fever symptoms C0030372 Fever, pappataci DiseaseOntology|MalaCards C0428977 Pulse rate decrease C1864910 Glutamine deficiency, congenital MalaCards|HPO C0034150 Skin purpura C0398691 Hyperimmunoglobulinemia d MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0036205 Sarcoidosis, pulmonary HSDN C2315100 Pediatric failure to thrive C0265965 Dyskeratosis congenita MalaCards C0023012 Delay language C1857355 Leigh syndrome , french canadian type HPO C0036572 Convulsion C0019554 Dislocate hip HSDN C0027497 Queasy C0023860 Listeriosis DiseaseOntology|MalaCards C0232466 Feeding difficulty C2931168 Hemangiomas, and cutaneous and intracranial vascular deformations MalaCards C0853986 Lymphocytes decreased C0877024 Schimke immunoosseous dysplasia OrphaNet|HPO|MalaCards C0162298 Stiffness joints C1961835 Gaucher disease, type 1 MalaCards C0030552 Paralysis partial C0034345 Pyruvate dehydrogenase complex deficiency disease HSDN C0030193 Sense of pain C0020875 Ileal diseases HSDN C4085211 Pain distress question C1879737 Aromatherapy and essential oils HSDN C2911647 Weight gain adverse event C3665624 Serum calcium below normal HSDN C0018926 Emesis bloody C0005424 Biliary tract diseases HSDN C0162298 Stiffness joints C1859316 Cataract-alopecia-sclerodactyly syndrome OrphaNet|MalaCards C0027497 Queasy C1522133 High cholesterol level HSDN C0026821 Cramp C0039520 Tenosynovitis HSDN C0349588 Stature short C0795865 Chromosome 17, trisomy 17p OrphaNet|MalaCards C0013395 Indigestion C0017658 Glomerulonephritis HSDN C0002624 Amnesia retrograde C1269683 Major depressive disorder HSDN C0030975 Disorders perception C0238265 Encephalopathy, callosal demyelinating HSDN C0015230 Exanthem C0263584 Fixed drug eruption caused by phenolphthalein UMLS C4084767 Bothered by vomiting C0039494 Temporomandibular joint disorders HSDN C0036572 Convulsion C0398739 Congenital disorder of glycosylation, type 2c MalaCards|UMLS C0015672 Decreased energy C0029458 Osteoporosis, postmenopausal HSDN C1999266 Depression adverse event C1856492 Gaucher disease, type iiib HPO C0522224 Palsied C0936248 Chondroma HSDN C0008031 Pain chest C0018817 Atrial septal defects HSDN C2911647 Weight gain adverse event C2004491 Cicatrix HSDN C0036572 Convulsion C0003615 Appendicitis HSDN C0030193 Sense of pain C0024796 Marfan syndrome HSDN C0037763 Spasm C0268467 Hyperphenylalaninemia, bh4-deficient, b MalaCards|HPO C0042571 Vertigo subjective C1720416 Episodic ataxia type 2 (disorder) MalaCards|HPO|UMLS C0018524 Hallucinate C0003838 Arterial occlusive diseases HSDN C3463815 Feel fatigue C0079731 B-cell lymphomas HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0041296 Tuberculosis HSDN C0042798 Vision dim C1852551 Epithelial recurrent erosion dystrophy MalaCards C0349588 Stature short C0265756 Congenital atresia of larynx OrphaNet|MalaCards C0030552 Paralysis partial C0011570 Mental depression HSDN C0031911 Pigment deposition C0029454 Osteopetrosis MalaCards C0040822 D tremors C0003125 Anorexia nervosa HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0042514 Tachycardia, ventricular HSDN C0010200 Cough symptom C2911643 Encounter due to family history of osteoporosis HSDN C0030486 Extremity paralysis, lower C0037773 Spastic paraplegia, hereditary OrphaNet|MalaCards C3244654 Sore throat brand of benzocaine & menthol C0032371 Poliomyelitis MalaCards C0231218 Malaise generalized C1336369 Stage ivb carcinoma of liver cells UMLS C1963071 Back pain adverse event C1532253 Sedentary lifestyle HSDN C0242936 Center pain C0015663 Fasting HSDN C0029163 Hemorrhage mouth C0025202 Melanoma HSDN C0015230 Exanthem C0021368 Inflammation MalaCards C0027796 Neuralgias C0034530 Injury radiation HSDN C0018681 Headache, cephalalgia C0021051 Immunologic deficiency syndromes HSDN C0011124 Libido decreased C0855242 Disturbance in sexual arousal UMLS C0474368 Childbirth pain C0600564 Self-efficacy HSDN C4085210 Usual severity pain C0026277 Mixed salivary gland tumor HSDN C1962972 Proteinuria adverse event C0013080 Down syndrome HSDN C0237326 Defecation pain C3150705 Foxg1 syndrome HPO C0030193 Sense of pain C0026936 Mycoplasma infections HSDN C0271215 Blindness legal C1848917 Tay-sachs disease, pseudo-ab variant HPO C3854173 Pre-renal acute kidney injury C0268742 Membranoproliferative glomerulonephritis, type i MalaCards C0018991 Paralysis one side of body C0243010 Viral encephalitis HSDN C4084766 Vomiting C0037313 Sleep HSDN C4084727 Cough frequency C0854421 Hanta viral infections MalaCards C0036572 Convulsion C0344479 Spinal cord myelodysplasia HSDN C0015672 Decreased energy C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C0014591 Bleeding nose C0040015 Thrombasthenia MalaCards|HPO C0034150 Skin purpura C0025874 Metrorrhagia HSDN C0026884 Muteness C0036341 Schizophrenia HSDN C0242936 Center pain C0026691 Mucocutaneous lymph node syndrome HSDN C0518090 Frequency of pain question C0282550 Persian gulf syndrome HSDN C0000737 Abdomen pain C0334287 Fibrolamellar hepatocellular carcinoma UMLS C0557874 Global developmental delay C2931006 Congenital disorder of glycosylation type 1l MalaCards C3815497 Cough C0000833 Abscess HSDN C0036572 Convulsion C0700208 Acquired scoliosis HSDN C0242936 Center pain C0033289 Family relationship, professional HSDN C0040034 Thrombocytopenia C0036489 Sea-blue histiocyte syndrome OrphaNet|HPO|MalaCards C0019079 Bloody sputum C1336145 Stage ib squamous cell lung carcinoma UMLS C0751495 Seizure focal C0422855 Epileptic vertigo UMLS C0518090 Frequency of pain question C0031269 Peutz-jeghers syndrome HSDN C3203358 Alveolar hypoventilation C0020538 Hypertensive disease HSDN C0018784 Deafness sensorineural C0015927 Intrauterine fetal demise HSDN C0018681 Headache, cephalalgia C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C0037036 Increased salivation C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C2232697 Mood symptoms C0085633 Mood swings UMLS C0042024 Urine incontinence C0206171 Community acquired infections HSDN C0028738 Nystagmus C3550904 Epileptic encephalopathy, early infantile, 36 MalaCards C0019079 Bloody sputum C3887588 Tracheopathia osteoplastica MalaCards C0030193 Sense of pain C4081911 Neuralgia of right upper limb UMLS C0149651 Clubbing C0152021 Congenital heart disease UMLS C0012833 Dizzy C0002986 Fabry disease MalaCards|HSDN|HPO C1384666 Decreased hearing C2675235 Deafness, autosomal recessive 1b MalaCards|HPO C0030193 Sense of pain C0038013 Ankylosing spondylitis DiseaseOntology|MalaCards C0027066 Myoclonic jerking C0021655 Insulin resistance HSDN C3887873 Hearing loss C0029456 Osteoporosis HSDN C3887638 Failure to thrive in infant C0015668 Fat necrosis HSDN C0042798 Vision dim C0702221 Tactual discrimination HSDN C0005745 Blepharoptosis C3809221 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 MalaCards C0018524 Hallucinate C0025289 Meningitis HSDN C0013456 Pain ear C1300028 Disorder characterised by pain UMLS C1549543 Administration method - pain C0035333 Retinitis HSDN C2237041 Shox gene with short stature C0543514 Glycogen storage disease ixb HPO C0577583 Swelling of body structure C0236003 Mucosal swelling UMLS C0002962 Angina C0014457 Eosinophilia HSDN C2203646 Jaundice C0032269 Pneumococcal infections HSDN C4084766 Vomiting C0305062 Tetanus toxoids HSDN C2024878 Cardiovascular surgery result: dyspnea C0007097 Carcinomas HSDN C2911645 Weight loss adverse event C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0027497 Queasy C0751908 Vestibular neuronitis HSDN C1557397 Adverse event associated with pain C0016724 Froehlich's syndrome HSDN C4085211 Pain distress question C0037354 Smallpox HSDN C0518090 Frequency of pain question C0032227 Pleural effusion disorder HSDN C4085317 Diarrhea frequency C2117118 X-ray of toe: deformity contracture HSDN C0012833 Dizzy C0395937 Structural anomaly of the cochlea and vestibular labyrinth UMLS C0026821 Cramp C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards|UMLS C0015469 Facial paralysis C0520679 Sleep apnea, obstructive HSDN C0917816 Deficiency mental C3151036 Chromosome 1p32-p31 deletion syndrome HPO C0033774 Skin pruritus C1842839 Hypotrichosis 6 MalaCards|HPO C0857305 Thrombocytopenia purpura C0221056 Adult type dermatomyositis HSDN C4085210 Usual severity pain C0029422 Osteochondrodysplasias HSDN C1961131 Cough adverse event C1535939 Pneumocystis jiroveci pneumonia HSDN C0037316 Not enough sleeping C0016989 Galvanic skin response HSDN C0023012 Delay language C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C0751837 Gait ataxic C0035372 Rett syndrome MalaCards|HPO|UMLS C0002622 Amnesias C0038263 Stereognoses HSDN C3898969 Have been vomiting C0005695 Bladder neoplasm HSDN C0037036 Increased salivation C2678415 Hyperphenylalaninemia, bh4-deficient, due to partial pts deficiency HPO C0011991 Loose stools C0024638 Class ii division 2 malocclusion HSDN C0037763 Spasm C0018802 Congestive heart failure HSDN C0036572 Convulsion C1827284 Intractable occipital lobe epilepsy UMLS C0027497 Queasy C0013289 Duodenal diseases HSDN C0242936 Center pain C0020619 Hypogonadism HSDN C1963184 Nystagmus adverse event C0162635 Angelman syndrome MalaCards|HPO C0028738 Nystagmus C1849140 Spastic ataxia, charlevoix-saguenay type MalaCards|HPO C3815497 Cough C2609414 Acute kidney injury HSDN C2984058 Have pain C0023801 Lipomatosis HSDN C4085210 Usual severity pain C0029463 Osteosarcoma OrphaNet|HSDN|HPO C1069915 Vertigo C1956391 Temporal arteritis MalaCards|HPO C0012833 Dizzy C1847843 Episodic ataxia, type 4 MalaCards C3887873 Hearing loss C0002395 Alzheimer's disease HSDN C0349588 Stature short C1860118 Acro fronto facio nasal dysostosis OrphaNet|MalaCards C0018772 Deafness C1854368 Cardiomyopathy, dilated, 1j MalaCards C0036572 Convulsion C0796264 Young-hughes syndrome OrphaNet|MalaCards C0917816 Deficiency mental C2937419 Chromosome x pentasomy OrphaNet|MalaCards C1962972 Proteinuria adverse event C0085298 Sudden cardiac death HSDN C0009421 Comatose C0342728 3-methylglutaconic aciduria type 1 MalaCards|HPO C3641756 Have diarrhea C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C0700078 Deep tendon reflex decrease C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C4084784 Diarrhea C0025061 Disease of mediastinum HSDN C4084769 Vomiting frequency C0431109 Choroid plexus carcinoma HPO C0278155 Taste blindness C0233746 Perceptual disturbance UMLS C4084724 Usual severity constipation C0264743 Rheumatic fever without heart involvement MalaCards C4084769 Vomiting frequency C0311375 Arsenic poisoning HSDN C4084802 Usual severity diarrhea C0038436 Post-traumatic stress disorder HSDN C0221166 Paraparesis C0026707 Mucopolysaccharidosis iv HSDN C0018681 Headache, cephalalgia C0030354 Papilloma HSDN C0428977 Pulse rate decrease C1869118 Hypothyroidism, congenital, due to thyroid dysgenesis HPO C3898969 Have been vomiting C0085693 Acute appendicitis nos (disorder) MalaCards C0041657 Consciousness loss C3714639 Exit block by ecg finding HSDN C4084766 Vomiting C0020303 Hydropneumothorax HSDN C0332573 Macula C1844376 Granulomatous disease, chronic, x-linked MalaCards C1963071 Back pain adverse event C2945560 Hemolytic HSDN C0026821 Cramp C0035435 Rheumatism HSDN C2315100 Pediatric failure to thrive C1849157 Insulin-like growth factor i, resistance to MalaCards C0020580 Decreased sensation C0027765 Nervous system disorder HSDN C0022107 Fussiness C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards|HPO C1963184 Nystagmus adverse event C0025235 Melkersson-rosenthal syndrome MalaCards C3463815 Feel fatigue C2347126 Microscopic polyarteritis HSDN C0018784 Deafness sensorineural C0376524 Branchio-oculo-facial syndrome MalaCards|HPO C0085602 Polydypsia C0043207 Wolfram syndrome OrphaNet|HPO|MalaCards C4084726 Distress cough C0011603 Dermatitis HSDN C3539023 Pelvic pain increasing in frequency C0001580 Adolescent behavior HSDN C0030554 Abnormal sensation C2347126 Microscopic polyarteritis MalaCards C0042940 Disorder of voice C0023343 Leprosy HSDN C0018784 Deafness sensorineural C1856899 Cutaneous albinism hermine phenotype OrphaNet|MalaCards C0522224 Palsied C0020757 Ichthyoses HSDN C0009421 Comatose C0019699 Hiv seropositivity HSDN C3463815 Feel fatigue C0852007 Scleroderma and associated disorders OrphaNet C4085548 Usual severity dizziness C0752143 Intracranial thrombosis HSDN C1963065 Apnea adverse event C0018621 Hay fever HSDN C4084766 Vomiting C0233629 Thinking and speaking disturbances HSDN C0033774 Skin pruritus C0015745 Ingestive behavior HSDN C0013604 Edematous C0021603 Sleep initiation and maintenance disorders HSDN C0234523 Apraxia, classic C0019542 Higher nervous activity HSDN C0020455 Hypergammaglobulinemia C3809031 Neutropenia, severe congenital, 5, autosomal recessive MalaCards C4085210 Usual severity pain C0206633 Angiomyolipoma HSDN C0030193 Sense of pain C3887650 Adult rickets HSDN C0860591 Congestion of lower extremities C0007222 Cardiovascular diseases UMLS C0013404 Respiratory difficulty C0022665 Kidney neoplasm HSDN C0851578 Disorder sleep C0031350 Pharyngitis HSDN C1963091 Diarrhea adverse event C3888013 Hypnoses HSDN C4085549 Dizziness C0017636 Glioblastoma HSDN C0013395 Indigestion C0085681 Hyperphosphatemia (disorder) HSDN C0007814 Cerebrospinal fluid otorrhea C0039145 Syringomyelia and syringobulbia HSDN C2032396 Pelvic pain on the right C0035358 Retroperitoneal neoplasm HSDN C2984058 Have pain C0031069 Familial mediterranean fever HSDN C0037316 Not enough sleeping C0004153 Atherosclerosis HSDN C0002622 Amnesias C0340629 Aortic aneurysm without mention of rupture nos HSDN C3641756 Have diarrhea C3495559 Juvenile arthritis HSDN C0557874 Global developmental delay C0265962 Ichthyosis linearis circumflexa OrphaNet|HPO|MalaCards C0332563 Papulae C1275122 Familial multiple trichoepitheliomata OrphaNet|HPO|MalaCards C0011991 Loose stools C0023241 Legionnaires' disease MalaCards C4084897 Sleep disturbance subordinate domain C0266526 Norrie disease MalaCards|HPO C0522224 Palsied C0015414 Eye neoplasms HSDN C2919142 Short stature adverse event C1845450 Cubitus valgus with mental retardation and unusual facies MalaCards C0423665 Hand joint pain C2105255 Compression arthralgia of hand UMLS C0030193 Sense of pain C0009862 Contraception behavior HSDN C2096293 Ent surgical result ear vertigo C0000768 Congenital abnormality HSDN C0019209 Large liver C0001768 Agammaglobulinemia MalaCards C0038506 Stutter C0019829 Hodgkin disease HSDN C0151908 Dry skin C1863204 Adult syndrome OrphaNet|UMLS|HPO|MalaCards C4085211 Pain distress question C0040443 Avulsed tooth HSDN C2984058 Have pain C0014856 Esophageal fistula HSDN C4084773 Bothered by weight gain C0021799 Interprofessional relations HSDN C4084769 Vomiting frequency C0919267 Ovarian neoplasm HSDN C4084724 Usual severity constipation C0037933 Spinal diseases HSDN C1557397 Adverse event associated with pain C0043251 Wounds and injuries HSDN C2203646 Jaundice C0041313 Hepatic tuberculosis DiseaseOntology|MalaCards C0004134 Dyssynergia C0022802 Kuru HSDN C0003811 Cardiac rhythm disturbance C1837845 Sick sinus syndrome 1, autosomal recessive MalaCards C0413252 Hypothermia due to exposure C0042826 Field visual HSDN C0004134 Dyssynergia C0043388 Bouba HSDN C0460137 Push down or depress C2936741 Syndrome xxyy OrphaNet|MalaCards C0020673 Hypothermia (central) (local) C0011881 Diabetic nephropathy HSDN C0042963 Symptoms vomiting C0033873 Psychiatry HSDN C0023530 Leukopenia C0030779 Pelger-huet anomaly MalaCards|HPO C0036396 Sciatica C0004936 Mental disorders HSDN C0004134 Dyssynergia C2609414 Acute kidney injury HSDN C0005745 Blepharoptosis C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C1069915 Vertigo C0010034 Corneal diseases HSDN C4085211 Pain distress question C2350530 Bronchopulmonary aspergillosis HSDN C1557397 Adverse event associated with pain C0039971 Thirst HSDN C0018784 Deafness sensorineural C0238288 Muscular dystrophy, facioscapulohumeral OrphaNet|HSDN|HPO|MalaCards C1963170 Hypothermia adverse event C0022758 Kap HSDN C0547030 Sensory perceptual alteration: visual C0278652 Cns tumor, childhood craniopharyngioma UMLS C0007758 Cerebellar ataxia C1858114 Huntington disease-like 3 (disorder) MalaCards C0009421 Comatose C0001144 Acne vulgaris HSDN C0042940 Disorder of voice C0015726 Focused anxiety HSDN C2242996 Tingling C0042138 Uterine neoplasms HSDN C0024031 Back pain lower back C0016658 Fracture bone HSDN C0751837 Gait ataxic C3472711 Spinocerebellar ataxia 36 MalaCards|UMLS C0018777 Deafness, conductive C1881674 Medical device emits smoke HSDN C0009806 Constipate C3146254 Stage iii colon cancer ajcc v7 UMLS C2984057 Have nausea C0700327 Clinical findings relating to memory HSDN C0042024 Urine incontinence C0042138 Uterine neoplasms HSDN C0011991 Loose stools C0268151 Classical galactosemia MalaCards|HPO|UMLS C0235045 Paresthesia mucosal C0030554 Paresthesia UMLS C0030552 Paralysis partial C0751799 Brain hemorrhage, traumatic HSDN C0003862 Pain joint C0024137 Lupus erythematosus, cutaneous OrphaNet C0030193 Sense of pain C0035445 Rheumatism and fibrositis unspecified UMLS C1963184 Nystagmus adverse event C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C0520909 Ponv C0002063 Alkalosis HSDN C4084788 Have dizziness C0002878 Anemia, hemolytic HSDN C0007758 Cerebellar ataxia C0041408 Turner syndrome HSDN C0522224 Palsied C0023434 Chronic lymphocytic leukemia HSDN C1963091 Diarrhea adverse event C0035229 Respiratory insufficiency HSDN C4084788 Have dizziness C0009324 Ulcerative colitis HSDN C0917799 Sleeping excessive C0085209 Bovine spongiform encephalitis MalaCards C3815497 Cough C1540912 Hypereosinophilic syndrome HSDN C4085222 Nausea C0036240 Response, satiety HSDN C4020887 Photodysphoria C2751309 Achromatopsia 5 MalaCards|HPO C0030193 Sense of pain C0036631 Seminoma HSDN C0012569 Double vision C0751814 Brain injuries, vascular HSDN C0030193 Sense of pain C0040583 Tracheal stenosis HSDN C1527344 Dysphonia C0031350 Pharyngitis HSDN C3814530 Skin vesicle C3887645 Job syndrome HPO C0012569 Double vision C3809991 Immunodeficiency, common variable, 10 MalaCards C1961131 Cough adverse event C0006272 Bronchiolitis obliterans HSDN C0085602 Polydypsia C3151482 Hypercalciuria, childhood, self-limiting HPO C4084767 Bothered by vomiting C0004048 Breathing HSDN C0028738 Nystagmus C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO C0349588 Stature short C0265326 Bannayan-riley-ruvalcaba syndrome OrphaNet|HPO|MalaCards C1963249 Tinnitus adverse event C0032962 Pregnancy complications HSDN C4084766 Vomiting C0004626 Pneumonia, bacterial HSDN C0024031 Back pain lower back C0033975 Psychotic disorders HSDN C0424755 Fever symptoms C0524910 Hepatitis c, chronic MalaCards|HSDN C0036572 Convulsion C0032229 Pleural neoplasms HSDN C3539891 Pelvic pain to the rear C0262655 Recurrent urinary tract infection HSDN C0233509 Mood hypersomnia C0233501 Physiological disturbances associated with mood UMLS C2032396 Pelvic pain on the right C2350572 Illness behavior HSDN C2984058 Have pain C0008521 Choroid diseases HSDN C0155552 Hearing loss mixed C0347555 Friction blister HSDN C0018681 Headache, cephalalgia C0027430 Nasal polyps HSDN C2024893 Cardiovascular surgery result: fatigue C0085409 Polyendocrinopathies, autoimmune HSDN C0242936 Center pain C0949691 Spondylarthropathies HSDN C0424755 Fever symptoms C2116082 Finding of thyroid nodule by palpation HSDN C0424755 Fever symptoms C0518449 Control of hip fracture risk HSDN C0518090 Frequency of pain question C0241910 Hepatitis, autoimmune HSDN C0008031 Pain chest C1963198 Pancreatitis adverse event HSDN C0751295 Memory loss or impairment C0917890 Pineocytoma OrphaNet|MalaCards C2911645 Weight loss adverse event C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C2032396 Pelvic pain on the right C0019065 Hemorrhage intraperitoneal HSDN C3887638 Failure to thrive in infant C0268542 Ornithine carbamoyltransferase deficiency HPO C0018772 Deafness C0265962 Ichthyosis linearis circumflexa MalaCards C4084768 Usual severity vomiting C0002895 Anemia, sickle cell HSDN C0034150 Skin purpura C0040015 Thrombasthenia MalaCards|HPO C4084724 Usual severity constipation C0038356 Stomach neoplasms HSDN C4085317 Diarrhea frequency C0017150 Gastrinoma OrphaNet|MalaCards C4084784 Diarrhea C0028796 Dermatitis, occupational HSDN C0241136 Skin pain C1275009 Painful operation scar UMLS C0009676 Confusion state C0027643 Neoplasm recurrence, local HSDN C0151889 Reflexes tendon increased C0220701 Retinitis pigmentosa 1 MalaCards C0015469 Facial paralysis C0342783 Deficiency of butyryl-coa dehydrogenase MalaCards|HPO C0004604 Pain back C0020541 Hypertension, portal HSDN C4084766 Vomiting C0026269 Mitral valve stenosis HSDN C0522224 Palsied C0037315 Sleep apnea syndromes HSDN C0041834 Erythematous condition C1855792 Ichthyosiform erythroderma, congenital, nonbullous, 1 MalaCards C4084775 Usual severity weight loss C0003047 Animal disease HSDN C0242936 Center pain C0028840 Ocular hypertension HSDN C0010038 Corneal opacity disorder C3151519 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 MalaCards C4050613 Anxiety C0036391 Schwartz-jampel syndrome MalaCards|HPO C4084775 Usual severity weight loss C0242216 Biliary calculi HSDN C0020615 Hypoglycemia nos C1864952 Hyperinsulinemic hypoglycemia, familial, 5 MalaCards C4084776 Weight loss C0033968 Psychotherapeutic technique HSDN C0040264 Ear ringing sound C0027627 Neoplasm metastasis HSDN C0005745 Blepharoptosis C1849157 Insulin-like growth factor i, resistance to MalaCards C1963091 Diarrhea adverse event C0036330 Schistosomiasis mansoni DiseaseOntology C0037317 Sleep disturbance C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO|UMLS C3641756 Have diarrhea C0003492 Aortic coarctation HSDN C2911645 Weight loss adverse event C0238067 Colitis, collagenous HSDN C0042024 Urine incontinence C3495801 Granulomatosis with polyangiitis HSDN C1963091 Diarrhea adverse event C0795956 Chylomicron retention disease MalaCards|HPO C0007758 Cerebellar ataxia C0023788 Whipple disease MalaCards|HSDN C0000737 Abdomen pain C1866983 Scleroderma, familial progressive MalaCards C4084726 Distress cough C0241158 Cicatrix skin HSDN C0018777 Deafness, conductive C0022521 Kartagener syndrome HSDN|HPO C1962976 Ventricular fibrillation adverse event C1859062 Long qt syndrome 3 HPO C1963242 Stomach pain adverse event C1304456 Congo hemorrhagic fever MalaCards C0009421 Comatose C0024117 Chronic obstructive airway disease HSDN C0042571 Vertigo subjective C3648213 Late effects of nontraumatic intracranial hemorrhage vertigo UMLS C0497406 Over weight C0032463 Polycythemia vera HSDN C0332573 Macula C0334092 Hamartomatous polyp MalaCards C0013604 Edematous C0024638 Class ii division 2 malocclusion HSDN C0015672 Decreased energy C0037997 Splenic diseases HSDN C2362324 Pediatric obesity C0003850 Arteriosclerosis HSDN C1963091 Diarrhea adverse event C0016154 Fish disease HSDN C2315100 Pediatric failure to thrive C0796147 Acrocallosal syndrome MalaCards|HPO C1962972 Proteinuria adverse event C1850331 Oculorenocerebellar syndrome OrphaNet|MalaCards C0242936 Center pain C0080178 Spina bifida HSDN C0151908 Dry skin C2677792 Riddle syndrome MalaCards|HPO|UMLS C0557874 Global developmental delay C3150924 Mental retardation, anterior maxillary protrusion, and strabismus MalaCards|HPO C2984057 Have nausea C0022410 Joint instability HSDN C3665346 Loss sight C0684324 Deficiency of phosphoglycerate kinase MalaCards C0007859 Pain neck C0221204 Lytic lesion HSDN C3539020 Pelvic pain decreasing in frequency C0012979 Canine disease HSDN C0007859 Pain neck C0037286 Skin neoplasms HSDN C0000737 Abdomen pain C1333858 Grade 3 rectal adenocarcinoma UMLS C4049644 Depression C3494506 Pseudohypoparathyroidism, type ia HPO C0518090 Frequency of pain question C0023283 Leishmaniasis, cutaneous HSDN C1549543 Administration method - pain C0043255 Stab wound HSDN C2024893 Cardiovascular surgery result: fatigue C0031090 Periodontal diseases HSDN C1000483 Genus anemia C0039445 Hereditary hemorrhagic telangiectasia HPO C0013404 Respiratory difficulty C0242488 Acute lung injury HSDN C0036572 Convulsion C3489725 Pseudo-torch syndrome OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C1837819 Cerebrofrontofacial syndrome MalaCards C0020673 Hypothermia (central) (local) C0016542 Foreign body HSDN C2315100 Pediatric failure to thrive C1846044 Adrenomyodystrophy OrphaNet|MalaCards C1963065 Apnea adverse event C0029294 Orofaciodigital syndromes HSDN C0035229 Respiratory function impaired C0264743 Rheumatic fever without heart involvement MalaCards C0018772 Deafness C0015732 Fecal incontinence HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0013502 Echinococcosis HSDN C0575081 Abnormal gait C1851945 Dystonia 1, torsion, autosomal dominant OrphaNet|HPO|MalaCards C1963064 Anxiety adverse event C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C4084784 Diarrhea C0023434 Chronic lymphocytic leukemia HSDN C0009763 Conjunctiva inflammation C0406709 Hay-wells syndrome HPO C0043094 Weight gain C0031345 Pharyngeal diseases HSDN C1557397 Adverse event associated with pain C3463897 Hydatidiform mole, recurrent, 1 HSDN C0031315 Phantom limb pain C0042338 Herpesvirus 3, human HSDN C2096293 Ent surgical result ear vertigo C0085094 Head injury closed HSDN C0521663 Chronic progressive paraparesis C1290882 Chronic disease of nervous system UMLS C0086437 Joint hypermobility C4014294 Desbuquois dysplasia 2 MalaCards|UMLS C4084766 Vomiting C0029944 Drug overdose HSDN C0036572 Convulsion C0393701 Symptomatic lennox-gastaut syndrome UMLS C0026838 Spasticity muscle C3553449 Pontocerebellar hypoplasia, type 1b MalaCards|UMLS C0030552 Paralysis partial C3151403 Amyotrophic lateral sclerosis 14 with or without frontotemporal dementia HPO C1963065 Apnea adverse event C0039006 Swine--diseases HSDN C4084788 Have dizziness C0015408 Eye injury HSDN C0002965 Crescendo angina C0022658 Kidney diseases HSDN C0000727 Abdomen acute C0002940 Aneurysm HSDN C0018784 Deafness sensorineural C0016470 Food allergy HSDN C1971624 Appetite absent C0004238 Atrial fibrillation HSDN C2203646 Jaundice C1138434 Disease, x-linked genetic HSDN C2242996 Tingling C1319688 Blister dose form HSDN C4084727 Cough frequency C0398370 Lipedema HSDN C0042798 Vision dim C1841721 Achromatopsia 4 HPO C1263846 Attention deficit disorder with hyperactivity C1859252 Cerebrofaciothoracic dysplasia MalaCards C0018784 Deafness sensorineural C1850627 Keipert syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0040583 Tracheal stenosis HSDN C0010200 Cough symptom C0024214 Lymphangiectasis HSDN C4084723 Constipation C0006663 Calcinosis HSDN C0041105 Jaw spasm C0037304 Skull fracture HSDN C3541349 Syncope C0019159 Hepatitis a HSDN C0036572 Convulsion C0030299 Pancreatic pseudocyst HSDN C0026838 Spasticity muscle C0574084 3-methylglutaconic aciduria type 3 MalaCards|HPO|UMLS C0026884 Muteness C1851708 Encephalopathy, recurrent, of childhood MalaCards C0019079 Bloody sputum C0344315 Depressed mood HSDN C0034124 Pupillary disorder C0035334 Retinitis pigmentosa HSDN C0001707 Aerophagia C0009373 Colonic diseases HSDN C0241137 Skin pallor C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0006309 Brucellosis HSDN C0427055 Face weakness C1853926 Nonaka myopathy MalaCards|HPO C2029884 Hearing loss by exam C0020443 Hypercholesterolemia HSDN C2242996 Tingling C0428953 Ecg infarction myocardial HSDN C1963281 Vomiting adverse event C0022821 Kyphosis deformity of spine HSDN C0008031 Pain chest C0036202 Sarcoidosis OrphaNet|HPO|MalaCards C0030486 Extremity paralysis, lower C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0030193 Sense of pain C0014008 Empty sella syndrome HSDN C1963167 Memory impairment adverse event C1836148 Supranuclear palsy, progressive, 2 MalaCards C0033774 Skin pruritus C1335302 Pancreatic ductal adenocarcinoma UMLS C0020455 Hypergammaglobulinemia C0024121 Lung neoplasms HSDN C0020438 Hypercalciuria C0005283 Beta thalassemia HSDN C4084726 Distress cough C0221390 Non-bacterial thrombotic endocarditis HSDN C0018772 Deafness C0220754 Biotinidase deficiency OrphaNet|HPO|MalaCards C3829611 Nausea frequency C0009088 Cluster headache HSDN C2024878 Cardiovascular surgery result: dyspnea C0042138 Uterine neoplasms HSDN C0018777 Deafness, conductive C1548578 Location characteristic id - smoking HSDN C0151786 Weakness muscle C0004238 Atrial fibrillation HSDN C4084766 Vomiting C0175683 Citrullinemia HPO C0018784 Deafness sensorineural C1845526 Mental retardation, x-linked 46 HPO C3898969 Have been vomiting C0038013 Ankylosing spondylitis HSDN C3887638 Failure to thrive in infant C0268548 Hyperargininemia HSDN C0242936 Center pain C0002880 Autoimmune hemolytic anemia HSDN C0424755 Fever symptoms C0013578 Ectoparasitism HSDN C4085211 Pain distress question C0029443 Osteomyelitis HSDN C0424755 Fever symptoms C0010417 Cryptorchidism HSDN C0242936 Center pain C0027644 Neoplasm regression, spontaneous HSDN C4085549 Dizziness C0085096 Peripheral vascular diseases HSDN C1963063 Anorexia adverse event C0029340 Orthomolecular therapy HSDN C0033377 Caudal displacement C1861835 Cataract, aberrant oral frenula, and growth retardation OrphaNet|MalaCards C0035232 Diaphragmatic paralysis C0600260 Lung diseases, obstructive HSDN C0262527 Intermittent abdominal pain C0334299 Carcinoid tumor no icd-o subtype MalaCards C0600142 Flash hot C0033968 Psychotherapeutic technique HSDN C0178417 Anhedonia C0525043 Attachment disorder reactive HSDN C1263846 Attention deficit disorder with hyperactivity C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C0017565 Gingiva hemorrhage C0011311 Dengue fever MalaCards C0015970 Fever unknown origin C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0917799 Sleeping excessive C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0027497 Queasy C0270639 Lateral sinus thrombosis HSDN C0013604 Edematous C0151620 Hypertensive encephalopathy HSDN C4084775 Usual severity weight loss C0002726 Amyloidosis HSDN C0917816 Deficiency mental C0007965 Chediak-higashi syndrome MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0017178 Gastrointestinal diseases HSDN C0009806 Constipate C2217035 Stage iia colon cancer UMLS C0423823 Nail thinness C1857069 Schopf-schulz-passarge syndrome (disorder) MalaCards|HPO C4084775 Usual severity weight loss C0013808 Electroconvulsive therapy HSDN C1963086 Confusion adverse event C0027686 Pathologic neovascularization HSDN C0010520 Skin cyanosis C0037274 Dermatologic disorders HSDN C0038002 Spleen enlargement C0268131 Omp decarboxylase deficiency MalaCards C0011991 Loose stools C0005686 Urinary bladder diseases HSDN C0520909 Ponv C1963064 Anxiety adverse event HSDN C0020450 Hyperemesis gravidarum C0032962 Pregnancy complications UMLS C0917816 Deficiency mental C2930900 Beta-sarcoglycanopathy MalaCards C0015672 Decreased energy C0032269 Pneumococcal infections HSDN C4085210 Usual severity pain C0041954 Ureteral diseases and syndromes HSDN C2029884 Hearing loss by exam C0036472 Scrub typhus HSDN C0036572 Convulsion C0019080 Hemorrhage HSDN C4084769 Vomiting frequency C3241945 Melena due to gastrointestinal hemorrhage HSDN C4084776 Weight loss C0027661 Neoplasms, hormone-dependent HSDN C0013456 Pain ear C0019284 Diaphragmatic hernia HSDN C0013404 Respiratory difficulty C1332556 Biphasic pulmonary blastoma UMLS C1549543 Administration method - pain C1548484 Rheumatic fever vaccine HSDN C0040034 Thrombocytopenia C3554663 Bleeding disorder, platelet-type, 15 MalaCards C0042963 Symptoms vomiting C0267172 Habit vomiting UMLS C2237041 Shox gene with short stature C0085920 Brachial neuralgia MalaCards C0000737 Abdomen pain C1550672 Specimen type - ulcer HSDN C0041105 Jaw spasm C0008925 Cleft palate HSDN C1963087 Constipation adverse event C0220981 Metabolic acidosis HSDN C1090821 Sepsis C0015773 Felty syndrome MalaCards C0036572 Convulsion C1836797 Combined oxidative phosphorylation deficiency 1 MalaCards|HPO C0086437 Joint hypermobility C1970414 Osteogenesis imperfecta, type v MalaCards|HPO C0017181 Gastrointestinal bleed C0043397 Yellow fever, jungle MalaCards C0557874 Global developmental delay C0175703 Thrombocytopenia-absent radius syndrome MalaCards|HPO C0040822 D tremors C3810285 Myopathy with extrapyramidal signs MalaCards C0413252 Hypothermia due to exposure C0014804 Erythromelalgia MalaCards|HPO C0241210 Speaking delay C3149276 Chromosome 16p12.1 deletion syndrome, 520-kb HPO C0030552 Paralysis partial C0015624 Fanconi syndrome HSDN C4084784 Diarrhea C1856127 Bile acid synthesis defect, congenital, 2 MalaCards|HPO C1963252 Tremor adverse event C0030920 Peptic ulcer HSDN C0234146 Absent reflex C1859198 Charcot-marie-tooth disease, type 4a (disorder) MalaCards|HPO C0007758 Cerebellar ataxia C1850406 Navajo neurohepatopathy MalaCards|HPO C1860844 Sparse, thin hair C0220744 Multiple gastrointestinal atresias (disorder) MalaCards C0013604 Edematous C3469521 Fanconi anemia, complementation group a (disorder) HSDN C0085631 Abnormal excitement C0919267 Ovarian neoplasm HSDN C0917816 Deficiency mental C0796066 Microcephaly-cervical spine fusion anomalies MalaCards C0522224 Palsied C0007282 Carotid stenosis HSDN C2203646 Jaundice C0022665 Kidney neoplasm HSDN C0022660 Acute kidney failure C0026764 Multiple myeloma OrphaNet|HPO C2242996 Tingling C1258666 Myxoid cyst HSDN C3815497 Cough C0276119 Q-fever pneumonia MalaCards C0031911 Pigment deposition C0014170 Endometrial neoplasms MalaCards C0917967 Pupil function anomaly C0751254 Creutzfeldt-jakob disease, familial MalaCards C0375564 Abdominal or pelvic swelling, mass, or lump, other specified site; multiple sites C0810319 Other and unspecified gastrointestinal disorders UMLS C4084775 Usual severity weight loss C3541994 Drug hypersensitivity syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0001818 Agoraphobia HSDN C0427190 Ataxia, truncal C1836395 Spinocerebellar ataxia 26 HPO|UMLS C4084775 Usual severity weight loss C1691228 Cystic kidney diseases HSDN C0009806 Constipate C3711749 Nonsyndromic holoprosencephaly MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0043352 Xerostomia HSDN C0007758 Cerebellar ataxia C0038819 Siriasis HSDN C0497247 Blood pressure elevation C0751039 Cockayne syndrome, type i HPO C0012833 Dizzy C0264766 Rheumatic mitral stenosis HSDN C0600142 Flash hot C0025874 Metrorrhagia HSDN C0600142 Flash hot C0003469 Anxiety disorders HSDN C4085211 Pain distress question C0014059 Encephalomyelitis, acute disseminated HSDN C0034124 Pupillary disorder C0014065 Congenital cerebral hernia HSDN C0018784 Deafness sensorineural C1527429 Increased blood npn HSDN C3898969 Have been vomiting C0025149 Medulloblastoma HSDN C3274924 Have been coughing C0032533 Polymyalgia rheumatica MalaCards C1557397 Adverse event associated with pain C0080233 Tooth loss HSDN C0018681 Headache, cephalalgia C1963067 Atrial fibrillation adverse event HSDN C0018772 Deafness C0752166 Bardet-biedl syndrome MalaCards|HPO C0019209 Large liver C0086649 Mps iii c HPO C0019209 Large liver C1291329 Transaldolase deficiency MalaCards|HPO C0233844 Awkwardness C1850442 Ceroid lipofuscinosis, neuronal, 5 MalaCards|HPO|UMLS C3697716 Acute flaccid paralysis C0032371 Poliomyelitis MalaCards C0013428 Painful urination C1511206 Bladder urachal squamous cell carcinoma UMLS C2919142 Short stature adverse event C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C0027497 Queasy C0035242 Respiratory tract diseases HSDN C3146279 Coma C0795623 Hepatitis a vaccine, inactivated HSDN C0036572 Convulsion C1636667 Disorder characterized by eosinophilia HSDN C0011991 Loose stools C0039231 Tachycardia HSDN C0149793 Transient monocular blindness C0423772 Cutaneous fistula HSDN C0018777 Deafness, conductive C2936904 Opitz gbbb syndrome, x-linked MalaCards C4085317 Diarrhea frequency C0023473 Myeloid leukemia, chronic HSDN C2029884 Hearing loss by exam C0008370 Cholestasis HSDN C0231791 In toe C0796110 Pallister syndrome 1 MalaCards C0007166 Cardiac output decreased C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0018524 Hallucinate C0018801 Heart failure HSDN C0015672 Decreased energy C0018798 Congenital heart defects HSDN C0020458 Hyperhydrosis C1848814 Thymoma, familial MalaCards C0162292 Extraocular palsy C3150172 Mtdps8b MalaCards|HPO C4084726 Distress cough C0004364 Autoimmune diseases HSDN C0850758 Pain pelvic C0030455 Parametritis HSDN C0018991 Paralysis one side of body C0030297 Pancreatic neoplasm HSDN C0019214 Hepatosplenomegaly C0036330 Schistosomiasis mansoni DiseaseOntology C0019825 Voice hoarseness C0027743 Nerve compression syndrome HSDN C4085211 Pain distress question C0334409 Leydig cell tumor, benign HSDN C2032396 Pelvic pain on the right C0000768 Congenital abnormality HSDN C0332573 Macula C0406775 Symmetrical dyschromatosis of extremities OrphaNet|HPO|MalaCards C0020305 Fetal edema C0029422 Osteochondrodysplasias HSDN C0018772 Deafness C0042018 Urinary calculi HSDN C0000727 Abdomen acute C0036916 Sexually transmitted diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1963215 Pneumothorax adverse event HSDN C0034151 Hyperglobulinemic purpura C0024305 Lymphoma, non-hodgkin HSDN C0575081 Abnormal gait C1855606 Burton syndrome MalaCards C0011991 Loose stools C2931189 Neural crest tumor MalaCards C0018772 Deafness C0009395 Color perception HSDN C2024893 Cardiovascular surgery result: fatigue C0029463 Osteosarcoma HSDN C0030975 Disorders perception C0013502 Echinococcosis HSDN C0042928 Paralysis vocal cord C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0003962 Ascites C0033822 Pseudomyxoma peritonei OrphaNet|MalaCards C4084784 Diarrhea C0032344 Poisoning aspects HSDN C4084724 Usual severity constipation C0878683 Pituitary dwarfism type 3 MalaCards C4084897 Sleep disturbance subordinate domain C0751362 Narcolepsy-cataplexy syndrome OrphaNet|MalaCards C0018775 Hearing loss bilateral C0005941 Bone diseases, developmental HSDN C0018681 Headache, cephalalgia C2717757 Retinocochleocerebral vasculopathies MalaCards C0010200 Cough symptom C0032285 Pneumonia UMLS C0013404 Respiratory difficulty C0019625 Sinus histiocytosis HSDN C1549543 Administration method - pain C0014550 Epilepsies, myoclonic HSDN C4042891 Sleep wake disorders C0014175 Endometriosis HSDN C4084766 Vomiting C0033885 Psychoanalytic interpretation HSDN C0019209 Large liver C0220748 Cartilage-hair hypoplasia MalaCards|HPO C0026838 Spasticity muscle C3280378 Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia UMLS C0851578 Disorder sleep C0001973 Alcoholic intoxication, chronic HSDN C2242996 Tingling C0037397 Behavior social HSDN C0014724 Burping C0022104 Irritable bowel syndrome HSDN C0349588 Stature short C1835494 Laryngeal web, familial OrphaNet|MalaCards C0151889 Reflexes tendon increased C3807567 Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome MalaCards C0042024 Urine incontinence C1333989 Familial meningioma MalaCards C3641756 Have diarrhea C0032045 Placenta disorders HSDN C0040460 Dental pain C0008065 Childhood behavior HSDN C0002965 Crescendo angina C0149649 Cholesterol embolism HSDN C0018772 Deafness C1847800 Waardenburg syndrome type 1 OrphaNet C0232466 Feeding difficulty C1859499 3-methylcrotonyl coa carboxylase 2 deficiency MalaCards C0020615 Hypoglycemia nos C0017925 Glycogen storage disease type vi OrphaNet|HPO|MalaCards C0159051 Shock without mention of trauma nos C0020683 Hypovolemic shock UMLS C0036572 Convulsion C3280153 Mental retardation, autosomal recessive 17 MalaCards C4085548 Usual severity dizziness C0006818 Campylobacter infection HSDN C0020672 Body temperature decreased C0023441 Leukemia, experimental HSDN C2237041 Shox gene with short stature C1862472 Oculomelic amyoplasia MalaCards|HPO C0030975 Disorders perception C0003467 Anxiety HSDN C0018772 Deafness C0025517 Metabolic diseases HSDN C0019825 Voice hoarseness C1334683 Endodermal sinus neoplasm of mediastinum UMLS C1384666 Decreased hearing C1832386 Diabetes mellitus, transient neonatal, 1 MalaCards|HPO C0013604 Edematous C0206171 Community acquired infections HSDN C0034150 Skin purpura C0016542 Foreign body HSDN C0013595 Eczematous dermatitis C1262481 Eosinophilic gastroenteritis MalaCards C0036572 Convulsion C0029139 Optical illusion HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017412 Genital diseases, male HSDN C0018524 Hallucinate C2931205 Usher syndrome, type 1a MalaCards C4085210 Usual severity pain C0002888 Anemia, megaloblastic HSDN C4085317 Diarrhea frequency C0007124 Noninfiltrating intraductal carcinoma HSDN C2984058 Have pain C0014013 Empyema, pleural HSDN C0028738 Nystagmus C3554209 Pontocerebellar hypoplasia, type 8 MalaCards C3463815 Feel fatigue C0033885 Psychoanalytic interpretation HSDN C2984058 Have pain C0023443 Hairy cell leukemia HSDN C2911645 Weight loss adverse event C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C3494358 Characteristic, prodromal C0428953 Ecg infarction myocardial HSDN C4084767 Bothered by vomiting C0006118 Brain neoplasms HSDN C0042798 Vision dim C0026709 Mucopolysaccharidosis vi MalaCards C1579931 Depressed - symptom C0566602 Primary sclerosing cholangitis MalaCards|HPO C0476273 Distress respiratory C1268935 Congenital thrombotic thrombocytopenic purpura HPO C4084724 Usual severity constipation C0035436 Rheumatic fever MalaCards|HSDN C0013362 Dysarthrias C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C0234533 Seizure generalized C3542499 Aminoacylase 2 deficiency MalaCards C1963087 Constipation adverse event C0027059 Myocarditis HSDN C2024878 Cardiovascular surgery result: dyspnea C0040185 Tibia fracture HSDN C1963281 Vomiting adverse event C0017160 Gastroenteritis DiseaseOntology C0018772 Deafness C0175699 Saethre-chotzen syndrome MalaCards|HPO C4049602 Hyperactivity C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C0576456 Poor feeding C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0035229 Respiratory function impaired C1854380 Nemaline myopathy 5 HPO C0518090 Frequency of pain question C3714644 Thymus neoplasms HSDN C0013404 Respiratory difficulty C0038661 Suicide HSDN C2096293 Ent surgical result ear vertigo C0036974 Shock HSDN C0042928 Paralysis vocal cord C1854336 Paragangliomas 3 MalaCards|HPO C4084768 Usual severity vomiting C0007194 Hypertrophic cardiomyopathy HSDN C4085210 Usual severity pain C0020640 Inherited factor ii deficiency HSDN C0349588 Stature short C0086652 Mucopolysaccharidosis type ivb MalaCards C0022346 Yellow skin C0262584 Carcinoma, small cell HSDN C2237041 Shox gene with short stature C0403548 Salcedo syndrome MalaCards C0086437 Joint hypermobility C0268353 Cutis laxa, x-linked MalaCards|HPO|UMLS C0030193 Sense of pain C0544796 Myositides, proliferative UMLS C4084766 Vomiting C0403447 Chronic kidney insufficiency HSDN C3146279 Coma C0022116 Ischemia HSDN C0917816 Deficiency mental C0271585 Isolated trh deficiency MalaCards C0086437 Joint hypermobility C1851801 Eds viib HPO C0013404 Respiratory difficulty C0997768 Glaucoma HSDN C3641755 Have constipation C1579931 Depressed - symptom HSDN C0151786 Weakness muscle C0342788 Renal carnitine transport defect OrphaNet|UMLS|HPO|MalaCards C0004134 Dyssynergia C1855565 Pyruvate dehydrogenase e2 deficiency MalaCards|HPO|UMLS C0086565 Liver function abnormal C0016952 Galactosemias MalaCards C0749870 Upper motor neuron sign C1968845 Primary lateral sclerosis, adult, 1 MalaCards|UMLS C0002965 Crescendo angina C0340464 Heartbeats ectopic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0556482 Protection sex HSDN C0014591 Bleeding nose C3888004 Hermansky-pudlak syndrome 5 MalaCards C3274924 Have been coughing C0011853 Diabetes mellitus, experimental HSDN C4084769 Vomiting frequency C0556346 Binge drinking HSDN C0349588 Stature short C2931876 Hirschsprung disease 1 MalaCards C0231218 Malaise generalized C2983424 Stage iv hepatocellular carcinoma UMLS C0042571 Vertigo subjective C0038160 Staphylococcal infections HSDN C0027066 Myoclonic jerking C0024115 Lung diseases HSDN C4042891 Sleep wake disorders C0517960 Neurological status: consciousness HSDN C0917816 Deficiency mental C4015261 Polyendocrine-polyneuropathy syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C1850553 Nephropathy deafness hyperparathyroidism OrphaNet|MalaCards C4084723 Constipation C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0004275 Attitude health HSDN C4084726 Distress cough C0001261 Actinomycosis HSDN C3898969 Have been vomiting C0024117 Chronic obstructive airway disease HSDN C0015672 Decreased energy C0001231 Acth syndrome, ectopic MalaCards C1069915 Vertigo C0001883 Airway obstruction HSDN C0024031 Back pain lower back C0717360 Disease lyme vaccine HSDN C0406569 Extensive congenital erosions, vesicles and reticulate scarring C0242354 Disorder birth UMLS C0038002 Spleen enlargement C0206141 Idiopathic hypereosinophilic syndrome HPO C1090821 Sepsis C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0030193 Sense of pain C1275235 Parosteal nodular fasciitis UMLS C0004134 Dyssynergia C4014531 Epileptic encephalopathy, early infantile, 24 MalaCards C1963281 Vomiting adverse event C0000833 Abscess HSDN C4084774 Have weight loss C0679360 Foodborne disease HSDN C0011991 Loose stools C0002874 Aplastic anemia HSDN C0751837 Gait ataxic C0752155 Central nervous system vascular malformations HSDN C2107732 Consistent heat intolerance C4048800 Telomeric 22q13 monosomy syndrome MalaCards C4084768 Usual severity vomiting C3541306 Plasmodium measurement HSDN C3539895 Pelvic pain occurs with bowel movement C0033038 Ejaculatio praecox HSDN C0557874 Global developmental delay C1306856 Megaloblastic anemia due to inborn errors of metabolism MalaCards C0000737 Abdomen pain C0038644 Sudden infant death syndrome HSDN C0086439 Activity decreased C0524851 Neurodegenerative disorders HSDN C0040259 Tinea pedis C0453996 Tobacco smoking HSDN C0228505 Nodules C0085568 Buruli ulcer DiseaseOntology|MalaCards C0231218 Malaise generalized C1709568 Pleomorphic hepatocellular carcinoma UMLS C0018991 Paralysis one side of body C0036690 Septicemia HSDN C1963170 Hypothermia adverse event C0086543 Cataract nos HSDN C0242936 Center pain C0857007 Hyperbilirubinemia, neonatal HSDN C2911645 Weight loss adverse event C0026640 Mouth neoplasms HSDN C0917816 Deficiency mental C3280897 Joubert syndrome 15 MalaCards C3641755 Have constipation C0031212 Personality disorders HSDN C0018834 Brash C1862683 Townes brocks branchiootorenal like syndrome HPO C0008031 Pain chest C0017185 Gastrointestinal neoplasms HSDN C1384666 Decreased hearing C1568249 Usher syndrome, type ii HPO C0036572 Convulsion C2073625 X-ray of chest: pleural effusion HSDN C3463815 Feel fatigue C0033975 Psychotic disorders HSDN C0022346 Yellow skin C0861859 Bile duct signet ring cell carcinoma UMLS C4085211 Pain distress question C3714644 Thymus neoplasms HSDN C0030193 Sense of pain C0006107 Concussion HSDN C0020458 Hyperhydrosis C0003490 Aortic arch syndrome MalaCards C0030193 Sense of pain C0023283 Leishmaniasis, cutaneous HSDN C4085211 Pain distress question C0042850 Vitamin b deficiency HSDN C4042891 Sleep wake disorders C0035439 Rheumatic heart disease HSDN C0030193 Sense of pain C0019154 Hepatic vein thrombosis HSDN C0036396 Sciatica C0006118 Brain neoplasms HSDN C0028961 Urine output decreased C1366535 Avp gene HSDN C4084802 Usual severity diarrhea C0344435 Ventricular fibrillation by ecg finding HSDN C4085210 Usual severity pain C0020480 Hyperlipoproteinemia type iv HSDN C0424755 Fever symptoms C0376538 Blue-ear pig disease HSDN C3665347 Vision impaired C1853959 Birdshot chorioretinopathy OrphaNet|HPO|MalaCards C1963086 Confusion adverse event C2932716 Pseudohypoparathyroidism type 1c HPO C0043094 Weight gain C0042214 Vaccinia HSDN C1145670 Failure respiratory C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet C1384666 Decreased hearing C0018674 Head trauma HSDN C0235153 Sensory hallucination C0024776 Maple syrup urine disease HPO C1384666 Decreased hearing C0027627 Neoplasm metastasis HSDN C1963184 Nystagmus adverse event C1846564 Spastic paraplegia 7, autosomal recessive MalaCards|HPO C0848203 Male pelvic pain C0017416 Genital neoplasms, female HSDN C0030554 Abnormal sensation C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C2931007 Congenital disorder of glycosylation type 1x MalaCards|HPO C0009676 Confusion state C0004626 Pneumonia, bacterial HSDN C0043094 Weight gain C0018798 Congenital heart defects HSDN C2984058 Have pain C0362046 Prediabetes syndrome HSDN C1963091 Diarrhea adverse event C0264766 Rheumatic mitral stenosis HSDN C0413252 Hypothermia due to exposure C0025286 Meningioma HSDN C0036396 Sciatica C0005937 Bone cysts HSDN C1999266 Depression adverse event C0023788 Whipple disease OrphaNet|MalaCards C0237326 Defecation pain C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C0006430 Burning mouth syndrome HSDN C0015672 Decreased energy C0238386 Cronkhite-canada disease MalaCards C4084724 Usual severity constipation C0017181 Gastrointestinal hemorrhage HSDN C0152116 Torticollis spasmodic C0796279 Carnevale syndrome MalaCards|HPO C0018772 Deafness C0004933 Behavior modification technique HSDN C0038002 Spleen enlargement C2930674 Babesioses, human MalaCards C1527344 Dysphonia C1266119 Solitary fibrous tumor HSDN C0020538 Hbp C0013364 Dysautonomia, familial OrphaNet|HPO C0349588 Stature short C0265961 Erythrokeratodermia variabilis OrphaNet|HPO C0002962 Angina C2364172 Adherence to medication regime HSDN C4085210 Usual severity pain C0035795 Fever mountain rocky spotted HSDN C2984058 Have pain C0027962 Melanocytic nevus HSDN C1963063 Anorexia adverse event C0086922 Purpura rheumatoid OrphaNet|MalaCards C4084768 Usual severity vomiting C1555914 Psychologist - psychotherapy, group HSDN C0424755 Fever symptoms C0041324 Tuberculosis, osteoarticular HSDN C0034063 Edema lung C0085083 Ovarian hyperstimulation syndrome MalaCards|HPO C0027066 Myoclonic jerking C0677050 Manganese poisoning HSDN C2984057 Have nausea C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0041657 Consciousness loss C0265321 Wyburn-mason syndrome MalaCards C1963246 Sinus tachycardia adverse event C0011633 Dermatomyositis MalaCards C0030486 Extremity paralysis, lower C0032965 Pregnancy complications, infectious HSDN C3898969 Have been vomiting C1306759 Eosinophilic disorder HSDN C0085593 Chill C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0242936 Center pain C0025472 Mesenteric vascular occlusion HSDN C0000727 Abdomen acute C0007134 Renal cell carcinoma HSDN C1557397 Adverse event associated with pain C0006267 Bronchiectasis HSDN C4084724 Usual severity constipation C0004933 Behavior modification technique HSDN C0019079 Bloody sputum C0025202 Melanoma HSDN C0241137 Skin pallor C0265425 9p partial monosomy syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0005956 Bone marrow diseases HSDN C0391860 Diffuse inflammations C2231215 Nephrotic syndrome with interstitial diffuse nephritis UMLS C1963087 Constipation adverse event C0041582 Ulcer HSDN C1557397 Adverse event associated with pain C0517960 Neurological status: consciousness HSDN C0587246 Extremity weakness C1300202 Diaphyseal medullary stenosis with bone malignancy MalaCards C2984058 Have pain C0028432 Nose diseases HSDN C0007758 Cerebellar ataxia C0751039 Cockayne syndrome, type i HPO C0030794 Pelvis pain C0033348 Language program HSDN C2242996 Tingling C0238357 Hyperkalemic periodic paralysis HPO C4084725 Usual severity cough C0028796 Dermatitis, occupational HSDN C4084784 Diarrhea C0023794 Lipoidosis HSDN C4049644 Depression C0010308 Congenital hypothyroidism OrphaNet C0036572 Convulsion C1963674 Spinocerebellar ataxia 10 MalaCards|HPO|UMLS C0026838 Spasticity muscle C1855255 Pseudoarylsulfatase a deficiency MalaCards C0004941 Behavioral symptoms C1855675 Arima syndrome OrphaNet C1546759 Specimen source codes - pustule C0030360 Papillon-lefevre disease OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0015579 Family characteristics HSDN C4084727 Cough frequency C0013274 Patent ductus arteriosus HSDN C0518090 Frequency of pain question C1861964 Callosities, hereditary painful OrphaNet|MalaCards C0973461 Dysphasia C3806402 Epilepsy, focal, with speech disorder and with or without mental retardation MalaCards C1384666 Decreased hearing C0040560 Toxoplasmosis, congenital MalaCards C3146279 Coma C0031511 Pheochromocytoma HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0009375 Colonic neoplasms HSDN C0002622 Amnesias C0027932 Neurotic disorders HSDN C0013362 Dysarthrias C0033348 Language program HSDN C3494358 Characteristic, prodromal C0009244 Behavioral cognitive therapy HSDN C0018991 Paralysis one side of body C0007453 Cattle disease HSDN C0038002 Spleen enlargement C3150315 Aicardi-goutieres syndrome 1, autosomal dominant HPO C0030193 Sense of pain C0030186 Paget disease extramammary HSDN C0010520 Skin cyanosis C1956346 Coronary artery disease HSDN C0003467 Angst C1864112 Huntington disease-like 1 MalaCards|HPO C0030200 Intractable pain C0314657 Genetic predisposition HSDN C0018777 Deafness, conductive C0175702 Williams syndrome HSDN C4084802 Usual severity diarrhea C0023440 Acute erythroblastic leukemia HSDN C0426579 Anorexia symptom C1333764 Gastric cronkhite canada polyposis MalaCards C0522224 Palsied C0043528 Zoonoses HSDN C0024312 Lymphocytopenia C1860168 Achondroplasia, so-called, and severe combined immunodeficiency OrphaNet|MalaCards C0007758 Cerebellar ataxia C2750784 Spastic paraplegia 44, autosomal recessive (disorder) MalaCards|UMLS C3898969 Have been vomiting C0027794 Neural tube defects HSDN C0039870 Leanness C0009244 Behavioral cognitive therapy HSDN C0011991 Loose stools C0007124 Noninfiltrating intraductal carcinoma HSDN C0033774 Skin pruritus C0221391 Melanosis coli HSDN C3815497 Cough C0007570 Celiac disease HSDN C2024893 Cardiovascular surgery result: fatigue C0031511 Pheochromocytoma MalaCards|HSDN C0039070 Collapse fleeting C0023895 Liver diseases HSDN C1963249 Tinnitus adverse event C0011854 Diabetes mellitus, insulin-dependent HSDN C4085210 Usual severity pain C0006281 Congenital bronchogenic cyst HSDN C0030486 Extremity paralysis, lower C0405580 Adrenal cortical hypofunction HSDN C1557397 Adverse event associated with pain C0497580 Condylomata acuminata in men HSDN C4085211 Pain distress question C0001726 Affective symptoms HSDN C4084802 Usual severity diarrhea C0282207 Cronkhite-canada syndrome OrphaNet|MalaCards C0015469 Facial paralysis C0005941 Bone diseases, developmental HSDN C3887873 Hearing loss C0268233 Galactosialidosis MalaCards C0030193 Sense of pain C0206711 Pilomatrixoma HSDN C0151786 Weakness muscle C3553449 Pontocerebellar hypoplasia, type 1b MalaCards|UMLS C1963091 Diarrhea adverse event C0019189 Hepatitis, chronic HSDN C4085210 Usual severity pain C1852551 Epithelial recurrent erosion dystrophy MalaCards|HPO C0011991 Loose stools C0027643 Neoplasm recurrence, local HSDN C2911647 Weight gain adverse event C0011265 Presenile dementia HSDN C0034933 Abnormal reflexes C0000744 Abetalipoproteinemia HSDN C0018784 Deafness sensorineural C0406817 Collagenoma, familial cutaneous MalaCards C4085317 Diarrhea frequency C2939465 Deficiency of glucose-6-phosphate dehydrogenase HSDN C3463815 Feel fatigue C0035222 Respiratory distress syndrome, adult HSDN C0004093 Asthenia C0041310 Endocrine tuberculoses HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C3827868 Tachycardia by ecg finding C1858592 Carney triad OrphaNet|MalaCards C0004604 Pain back C0041948 Uremia HSDN C0008031 Pain chest C0748164 Pulmonary nodule multiple HSDN C0700078 Deep tendon reflex decrease C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C0016382 Cutaneous vascular engorgement C0020452 Hyperemia HSDN C2169806 Tic C0014550 Epilepsies, myoclonic HSDN C0518090 Frequency of pain question C0030469 Paranasal sinus diseases HSDN C0009676 Confusion state C0043049 Water intoxication HSDN C1384666 Decreased hearing C3502298 Lactic acidosis, fatal infantile MalaCards C0003862 Pain joint C0439840 Reflex motion descriptor HSDN C0003469 Anxiety disorder C0027873 Neuromyelitis optica MalaCards C4085548 Usual severity dizziness C0677866 Brain stem neoplasms HSDN C4085211 Pain distress question C0001849 Aids dementia complex HSDN C3815497 Cough C0085655 Polymyositis OrphaNet|MalaCards C1962957 Flushing adverse event C0025322 Premature menopause HSDN C0042024 Urine incontinence C1548484 Rheumatic fever vaccine HSDN C4084773 Bothered by weight gain C0040425 Tonsillitis HSDN C0000737 Abdomen pain C2217037 Stage iiia colon cancer UMLS C0020673 Hypothermia (central) (local) C0031212 Personality disorders HSDN C1961131 Cough adverse event C0036231 Sarcocystosis DiseaseOntology C1090821 Sepsis C0086438 Hypogammaglobulinemia MalaCards C0042571 Vertigo subjective C0013370 Amebic colitis HSDN C0010200 Cough symptom C1334969 Nodular lymphoid hyperplasia of lung UMLS C4084774 Have weight loss C0410422 Chronic multifocal osteomyelitis OrphaNet|MalaCards C0262384 Chest pain atypical C0022660 Kidney failure, acute UMLS C2138220 Cough quality C0043168 Whooping cough due to unspecified organism UMLS C1963170 Hypothermia adverse event C0030286 Pancreatic diseases HSDN C3829611 Nausea frequency C0016751 Hereditary fructose intolerance syndrome HPO C0042798 Vision dim C1857572 Corneal dystrophy and perceptive deafness OrphaNet|HPO C1069915 Vertigo C0018802 Congestive heart failure HSDN C1963137 Hydrocephalus adverse event C0812437 Oculo-dento-digital syndrome MalaCards|HPO C3274924 Have been coughing C0027686 Pathologic neovascularization HSDN C0020450 Hyperemesis gravidarum C2047432 Hyperemesis gravidarum as antepartum condition UMLS C4085210 Usual severity pain C0023702 Injury lightning HSDN C0030193 Sense of pain C0013010 Cerebral lateralization HSDN C1963071 Back pain adverse event C0004936 Mental disorders HSDN C4084727 Cough frequency C0035956 Rupture spontaneous HSDN C4084768 Usual severity vomiting C0206644 Histiocytoma, benign fibrous HSDN C0012569 Double vision C0032587 Polyradiculoneuropathy HSDN C0237326 Defecation pain C0010308 Congenital hypothyroidism OrphaNet|MalaCards C0026821 Cramp C0161408 Cranial nerve vii injuries HSDN C0497406 Over weight C0038454 Cerebrovascular accident HSDN C0232466 Feeding difficulty C1853490 22q13.3 deletion syndrome OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0085426 Gram-positive bacterial infections HSDN C3463815 Feel fatigue C0949690 Spondylarthritis HSDN C0518090 Frequency of pain question C0019101 Hemorrhagic fever with renal syndrome HSDN C0009398 Color vision defects C0302148 Blood clot HSDN C0850758 Pain pelvic C1261473 Sarcoma HSDN C0426579 Anorexia symptom C0206698 Cholangiocarcinoma HPO C0018784 Deafness sensorineural C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C4084725 Usual severity cough C3463824 Myelodysplastic syndrome HSDN C0344434 Atrial fibrillation ecg C1969099 Atrial fibrillation, familial, 5 MalaCards C0043094 Weight gain C0033968 Psychotherapeutic technique HSDN C0028738 Nystagmus C1848552 Methylmalonic aciduria and homocystinuria, cbld type MalaCards|HPO C3494358 Characteristic, prodromal C0812393 Cancer patients and suicide and depression HSDN C0349588 Stature short C0027831 Neurofibromatosis 1 HPO C0085128 Cardiac output elevated C0010340 Critical illness HSDN C0009421 Comatose C0032371 Poliomyelitis HSDN C0349588 Stature short C1848413 Trichothiodystrophy, type 1 MalaCards C0015672 Decreased energy C3542413 Cdisc adas-cog - comprehension HSDN C4084768 Usual severity vomiting C0035439 Rheumatic heart disease HSDN C4085211 Pain distress question C0271051 Macular retinal edema HSDN C0009806 Constipate C0040053 Thrombosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0002940 Aneurysm HSDN C3641756 Have diarrhea C1416865 Lipa gene HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0037999 Splenic neoplasms HSDN C0000737 Abdomen pain C0268314 Cholestasis-edema syndrome, norwegian type OrphaNet|MalaCards C0037763 Spasm C0011265 Presenile dementia HSDN C0034150 Skin purpura C0023903 Liver neoplasms HSDN C0010200 Cough symptom C0011884 Diabetic retinopathy HSDN C0042024 Urine incontinence C1855255 Pseudoarylsulfatase a deficiency MalaCards|HPO C0013362 Dysarthrias C0795889 Allan-herndon-dudley syndrome (ahds) MalaCards|HPO C4084723 Constipation C0007138 Carcinoma, transitional cell HSDN C0427055 Face weakness C0270968 Limb-girdle muscular dystrophy type 2h MalaCards|HPO|UMLS C0424755 Fever symptoms C0221390 Non-bacterial thrombotic endocarditis HSDN C0020538 Hbp C2930798 Alexanders leukodystrophy MalaCards C2911645 Weight loss adverse event C0023220 Leg injury HSDN C0030794 Pelvis pain C0027095 Myosarcoma HSDN C0033774 Skin pruritus C0019360 Herpes zoster disease DiseaseOntology|HSDN|MalaCards C3898969 Have been vomiting C3149848 Variegate porphyria, homozygous variant HPO C3541349 Syncope C0003850 Arteriosclerosis HSDN C0036572 Convulsion C0342737 3-hydroxyisobutyric aciduria MalaCards C0018681 Headache, cephalalgia C0041582 Ulcer HSDN C0746674 Muscle weakness generalized C0221021 Microangiopathic hemolytic anemia MalaCards C4042891 Sleep wake disorders C0010346 Crohn disease HSDN C0424810 Periorbital swelling C0340834 Hennekam lymphangiectasia lymphedema syndrome HPO C1963087 Constipation adverse event C0020255 Hydrocephalus HSDN C4085862 Bothered by nausea C0011303 Demyelinating diseases HSDN C2919142 Short stature adverse event C1850568 Nakajo syndrome MalaCards|HPO C0013404 Respiratory difficulty C1319853 Asthma, aspirin-induced HSDN C0349588 Stature short C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0020538 Hbp C3839866 Familial cerebral saccular aneurysm MalaCards C0242936 Center pain C0042214 Vaccinia HSDN C0026838 Spasticity muscle C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C0042928 Paralysis vocal cord C0037744 Perceptual spatial orientation HSDN C0030193 Sense of pain C1861172 Venous thromboembolism HSDN C0012833 Dizzy C0027859 Acoustic neuroma OrphaNet|HPO C1557397 Adverse event associated with pain C0752155 Central nervous system vascular malformations HSDN C0150055 Pain chronic C0699828 Serotonergic syndrome HSDN C3539890 Pelvic pain causes awakening at night C0042373 Vascular diseases HSDN C0019572 Hairiness C2748516 Spondylodysplasia and premature pubarche HPO C0270948 Neurogenic muscular atrophy C1850626 Nathalie syndrome MalaCards C4085222 Nausea C0004030 Aspergillosis HSDN C0018784 Deafness sensorineural C3553932 Deafness, autosomal recessive 98 MalaCards C0026838 Spasticity muscle C2930798 Alexanders leukodystrophy MalaCards C3641756 Have diarrhea C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0000737 Abdomen pain C0025517 Metabolic diseases HSDN C0026838 Spasticity muscle C1859093 Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0019114 Hemosiderosis HSDN C4084773 Bothered by weight gain C0018809 Heart neoplasm HSDN C0162834 Hyperpigmentation C1837756 Mandibuloacral dysplasia with type b lipodystrophy OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|HPO|MalaCards C0040822 D tremors C0751803 Brain stem hemorrhage, post traumatic HSDN C0030193 Sense of pain C0002949 Aneurysm, dissecting HSDN C1000483 Genus anemia C0472777 Hemoglobin e/beta thalassemia disease OrphaNet|HPO|MalaCards C0221263 Cafe au lait spot C0033785 Pseudarthrosis HSDN C3829611 Nausea frequency C0009404 Colorectal neoplasms HSDN C1997249 Neuralgia, pudendal C0043253 Trauma blunt HSDN C3641756 Have diarrhea C0595812 Fistula route HSDN C4082202 Sleep quality question C0024198 Lyme disease MalaCards C0413252 Hypothermia due to exposure C0013182 Drug allergy HSDN C1963065 Apnea adverse event C0020517 Hypersensitivity HSDN C4084766 Vomiting C0035956 Rupture spontaneous HSDN C4085548 Usual severity dizziness C0038358 Gastric ulcer HSDN C0034155 Thrombotic thrombocytopenic purpura C2931384 Moyamoya disease 1 HSDN C0242936 Center pain C0035078 Kidney failure HSDN C1963184 Nystagmus adverse event C3553960 Peroxisome biogenesis disorder 8b MalaCards C4084774 Have weight loss C0002792 Anaphylaxis HSDN C4085548 Usual severity dizziness C0004610 Bacteremia HSDN C0041105 Jaw spasm C1854540 Carney complex, type 2 MalaCards C0043094 Weight gain C0037274 Dermatologic disorders HSDN C0030794 Pelvis pain C1704376 Uterine corpus carcinosarcoma UMLS C4084768 Usual severity vomiting C0270726 Alexander disease HSDN C0497406 Over weight C0020443 Hypercholesterolemia HSDN C0851578 Disorder sleep C0028968 Olivopontocerebellar atrophies HSDN C4084762 Usual severity shortness of breath C0238990 Acute lower respiratory tract infection MalaCards C0019209 Large liver C1858328 Bile acid synthesis defect, congenital, 4 MalaCards|HPO C0036572 Convulsion C0917890 Pineocytoma MalaCards C1963087 Constipation adverse event C0004936 Mental disorders HSDN C0033774 Skin pruritus C0041234 Chagas disease HSDN C4084775 Usual severity weight loss C0153413 Malignant neoplasm of upper third of esophagus MalaCards C0003811 Cardiac rhythm disturbance C3809198 Pulmonary hypertension, primary, 4 MalaCards C0037036 Increased salivation C2931142 Dysharmonic skeletal maturation muscular fibre disproportion MalaCards C0000737 Abdomen pain C0022423 Judgement HSDN C1961131 Cough adverse event C0524688 Pneumonic plague DiseaseOntology|MalaCards C1963252 Tremor adverse event C0013080 Down syndrome HSDN C2984058 Have pain C0270327 Bedwetting HSDN C0030975 Disorders perception C0004153 Atherosclerosis HSDN C0010520 Skin cyanosis C0264303 Laryngomalacia HSDN C0002170 Alopecia disorders C0026363 Mohr-claussen syndrome MalaCards C4049644 Depression C0342739 Trimethylaminuria MalaCards|HPO C0151740 Intracranial hypertension C1834711 Cerebelloparenchymal disorder vi MalaCards C0150055 Pain chronic C0149931 Migraine disorders HSDN C4084774 Have weight loss C0020507 Hyperplasia HSDN C2919142 Short stature adverse event C1839874 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis HPO C0013404 Respiratory difficulty C0162871 Aortic aneurysm, abdominal HSDN C3641755 Have constipation C2936913 Porphyria, south african type HPO C0013604 Edematous C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome MalaCards C3463815 Feel fatigue C0041228 African trypanosomiasis HSDN C4084774 Have weight loss C0006105 Brain abscess HSDN C3898969 Have been vomiting C0013870 Electroconvulsive shock HSDN C1069915 Vertigo C0020649 Hypotension HSDN C3665492 Pigmentations C1706004 Anhydrotic ectodermal dysplasias MalaCards C0030552 Paralysis partial C0678236 Rare diseases HSDN C1260880 Nasal drip C1336264 Paranasal sinus cancer stage iii UMLS C3887873 Hearing loss C0796561 Melanoma vaccines HSDN C0497247 Blood pressure elevation C1851286 Ectopia lentis isolated MalaCards|HPO C4084768 Usual severity vomiting C0026848 Myopathy HSDN C0028738 Nystagmus C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C2984058 Have pain C0032788 Postoperative hemorrhage HSDN C1963086 Confusion adverse event C0015480 Disorder factitious HSDN C0037383 Sneeze C4048184 Trochlear nerve diseases HSDN C2919142 Short stature adverse event C1844853 Brachytelephalangic chondrodysplasia punctata HPO C0015672 Decreased energy C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0040822 D tremors C0021361 Female infertility HSDN C0019825 Voice hoarseness C1334636 Mature mediastinal teratoma UMLS C0015230 Exanthem C0477488 O spcf papulosquamous disor UMLS C0020505 Excessive eating C3151303 Obesity, hyperphagia, and developmental delay MalaCards|HPO C1963170 Hypothermia adverse event C0003486 Aortic aneurysm HSDN C0042024 Urine incontinence C1863704 Spastic paraplegia 8, autosomal dominant MalaCards|HPO C4084767 Bothered by vomiting C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4084802 Usual severity diarrhea C1963064 Anxiety adverse event HSDN C0013604 Edematous C0018482 Haemophilus infections HSDN C2984058 Have pain C0041834 Erythema HSDN C0033377 Caudal displacement C1862264 Bpes with duane retraction syndrome HPO C0040822 D tremors C1865818 Dystonia 7, torsion (disorder) UMLS C0009792 Consciousness disorder C0752347 Lewy body disease HSDN C4085211 Pain distress question C1962974 Chylothorax adverse event HSDN C0040259 Tinea pedis C0032787 Postoperative complications HSDN C1527344 Dysphonia C0023052 Laryngeal edema HSDN C4085317 Diarrhea frequency C0023092 Lassa fever OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0041974 Urethral stricture HSDN C4084776 Weight loss C0032227 Pleural effusion disorder HSDN C0522224 Palsied C0700327 Clinical findings relating to memory HSDN C0003550 Broca aphasia C0011581 Depressive disorder HSDN C0000737 Abdomen pain C0342859 Harderoporphyria HPO C4084775 Usual severity weight loss C0276275 Disease due to parvoviridae HSDN C0015230 Exanthem C0086922 Purpura rheumatoid OrphaNet|MalaCards C4084723 Constipation C0022665 Kidney neoplasm HSDN C0518090 Frequency of pain question C0034088 Pulmonary valve insufficiency HSDN C0034155 Thrombotic thrombocytopenic purpura C0002871 Anemia HSDN C0013421 Dystonia C0018565 Acquired deformity of hand, nos HSDN C0476273 Distress respiratory C2750080 Diamond-blackfan anemia 10 MalaCards|HPO C0270948 Neurogenic muscular atrophy C1510479 Neuralgic amyotrophy MalaCards C0013404 Respiratory difficulty C1336163 Stage iia adenocarcinoma of lung UMLS C0030552 Paralysis partial C0007286 Carpal tunnel syndrome HSDN C4084776 Weight loss C0042018 Urinary calculi HSDN C0242936 Center pain C0267941 Pancreatitis, acute necrotizing HSDN C0010520 Skin cyanosis C0022116 Ischemia HSDN C0036572 Convulsion C0026363 Mohr-claussen syndrome MalaCards C0018681 Headache, cephalalgia C0854912 Pineal germinoma HSDN C2024893 Cardiovascular surgery result: fatigue C0032001 Pituitary apoplexy MalaCards C1963249 Tinnitus adverse event C0439840 Reflex motion descriptor HSDN C3463815 Feel fatigue C1548578 Location characteristic id - smoking HSDN C1963064 Anxiety adverse event C3810225 Mental retardation, autosomal recessive 41 MalaCards C0004134 Dyssynergia C4014676 Ataxia-telangiectasia-like disorder 2 UMLS C3887873 Hearing loss C0000833 Abscess HSDN C0026603 Motion sickness C0036494 Mal de mer MalaCards C4084724 Usual severity constipation C0027663 Neoplasms, multiple primary HSDN C4084788 Have dizziness C0005974 Bone resorption HSDN C3463815 Feel fatigue C0024620 Primary malignant neoplasm of liver MalaCards C2984058 Have pain C0016659 Close fracture HSDN C3887873 Hearing loss C0036439 Scoliosis, unspecified HSDN C4020887 Photodysphoria C0271270 Oculovestibuloauditory syndrome MalaCards C0518090 Frequency of pain question C0027697 Nephritis HSDN C4084774 Have weight loss C1134719 Invasive ductal breast carcinoma HSDN C0019079 Bloody sputum C0243026 Sepsis HSDN C3641756 Have diarrhea C0029408 Degenerative polyarthritis HSDN C0151786 Weakness muscle C0010674 Cystic fibrosis HSDN C4084773 Bothered by weight gain C0018799 Heart diseases HSDN C0026858 Musculoskeletal pain C0158484 Acquired genu valgum HSDN C1959630 Eye pain adverse event C0014059 Encephalomyelitis, acute disseminated HSDN C4084784 Diarrhea C0000768 Congenital abnormality HSDN C3146279 Coma C0242342 Sheehan syndrome MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0020255 Hydrocephalus HSDN C0042571 Vertigo subjective C0037397 Behavior social HSDN C0042025 Urinary incontinence stress C0005967 Bone neoplasms HSDN C0002622 Amnesias C0039336 Gustatory sense HSDN C0018681 Headache, cephalalgia C0032987 Ectopic pregnancy HSDN C0024032 Birth weight subnormal C1836706 Hyperthyroidism, nonautoimmune MalaCards|HPO C0003811 Cardiac rhythm disturbance C0043194 Wiskott-aldrich syndrome OrphaNet|MalaCards C0003467 Angst C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0233514 Behavior abnormal C0002986 Fabry disease OrphaNet|MalaCards C3641756 Have diarrhea C0026552 Morphine dependence HSDN C0018681 Headache, cephalalgia C0008325 Cholecystitis HSDN C1963170 Hypothermia adverse event C0036202 Sarcoidosis MalaCards|HSDN|HPO C4084802 Usual severity diarrhea C0948089 Acute coronary syndrome HSDN C4084784 Diarrhea C1846171 Lissencephaly, x-linked, 2 HPO C0018681 Headache, cephalalgia C2984108 Nasopharyngeal carcinoma by ajcc v7 stage UMLS C1304408 Urticarial vasculitis C1304204 Urticarial vasculitis with monoclonal igm component, schnitzler UMLS C0018784 Deafness sensorineural C0340427 Familial dilated cardiomyopathy MalaCards|HPO C0239888 Headache recurrent C0002895 Anemia, sickle cell UMLS C1549543 Administration method - pain C0041330 Tuberculosis, spinal HSDN C0040822 D tremors C0521542 Brainstem infarct HSDN C3641756 Have diarrhea C0037322 Active eye movement sleep HSDN C0034151 Hyperglobulinemic purpura C0853697 Neutrophil count decreased HSDN C0018681 Headache, cephalalgia C3463824 Myelodysplastic syndrome HSDN C0413252 Hypothermia due to exposure C0013990 Pathological accumulation of air in tissues HSDN C0004134 Dyssynergia C3180937 15q11.2 microdeletion MalaCards|UMLS C4085222 Nausea C0009241 Cognition disorders HSDN C0424755 Fever symptoms C0042470 Guanarito haemorrhagic fever MalaCards C1000483 Genus anemia C2751310 Hyperuricemic nephropathy, familial juvenile 2 HPO C2911645 Weight loss adverse event C0027708 Nephroblastoma HSDN|HPO C0030554 Abnormal sensation C0001175 Acquired immunodeficiency syndrome HSDN C2024878 Cardiovascular surgery result: dyspnea C1443900 Inhalational botulism OrphaNet|MalaCards C4085211 Pain distress question C0026766 Multiple organ failure HSDN C1279888 Proteinuria of undiagnosed cause C0272258 Cryoglobulinemia, primary MalaCards C0036572 Convulsion C1263846 Attention deficit hyperactivity disorder HSDN C0020615 Hypoglycemia nos C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C0026838 Spasticity muscle C1136249 Mental retardation, x-linked HSDN C2911647 Weight gain adverse event C0030500 Animal parasitic disease HSDN C0015676 Mental fatigue C0006109 Brain damage, chronic HSDN C4042891 Sleep wake disorders C0002871 Anemia HSDN C2911645 Weight loss adverse event C3469186 Hemochromatosis, type 1 HSDN C0010038 Corneal opacity disorder C0086652 Mucopolysaccharidosis type ivb MalaCards C0003469 Anxiety disorder C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C1963249 Tinnitus adverse event C1962963 Osteoporosis adverse event HSDN C4085210 Usual severity pain C0013238 Dry eye syndromes HSDN C4085862 Bothered by nausea C0002994 Angioedema HSDN C0034155 Thrombotic thrombocytopenic purpura C0344315 Depressed mood HSDN C0030193 Sense of pain C0014536 Epidural tumor HSDN C0013421 Dystonia C1837355 Leukodystrophy, hypomyelinating, 2 MalaCards|HPO C0851578 Disorder sleep C1458155 Mammary neoplasms HSDN C2029884 Hearing loss by exam C0018674 Head trauma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0034884 Rectal fistula HSDN C0271215 Blindness legal C1849322 Sandhoff disease, infantile type HPO C0013395 Indigestion C0003855 Arteriovenous fistula HSDN C0030552 Paralysis partial C0003873 Rheumatoid arthritis HSDN C0013404 Respiratory difficulty C0026272 Mixed connective tissue disease OrphaNet|HSDN|MalaCards C4084774 Have weight loss C0008066 Child behavior disorders HSDN C0042798 Vision dim C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C0728710 Pupil constriction observed C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C0850758 Pain pelvic C0006434 Burn injury HSDN C0013428 Painful urination C1511189 Bladder hepatoid adenocarcinoma UMLS C0035078 Failure kidney C1857395 De toni-debre-fanconi syndrome HPO C1549543 Administration method - pain C0015814 Femur head necrosis HSDN C0004941 Behavioral symptoms C0751383 Juvenile neuronal ceroid lipofuscinosis OrphaNet|MalaCards C4084768 Usual severity vomiting C1963274 Vasculitis adverse event HSDN C0020672 Body temperature decreased C0007020 Carbon monoxide poisoning HSDN C0460137 Push down or depress C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C3539896 Pelvic pain occurs with urination C0040053 Thrombosis HSDN C3539020 Pelvic pain decreasing in frequency C0684743 Malignant neoplasm of muscle HSDN C4084776 Weight loss C0027439 Nasopharyngeal neoplasms HSDN C4084768 Usual severity vomiting C0033906 Psychological theories HSDN C0497406 Over weight C0006625 Cachexia HSDN C2984058 Have pain C0017412 Genital diseases, male HSDN C4084767 Bothered by vomiting C0314657 Genetic predisposition HSDN C1963184 Nystagmus adverse event C1838652 Split-hand/foot malformation 3 MalaCards C0271215 Blindness legal C0271270 Oculovestibuloauditory syndrome MalaCards C0013362 Dysarthrias C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C4085548 Usual severity dizziness C0344435 Ventricular fibrillation by ecg finding HSDN C0020615 Hypoglycemia nos C4040739 3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome MalaCards C0520909 Ponv C0015663 Fasting HSDN C0041834 Erythematous condition C1862892 Hereditary angioedema type ii HPO C0016382 Cutaneous vascular engorgement C0007192 Cardiomyopathy, alcoholic HSDN C2919142 Short stature adverse event C2931070 Schofer beetz bohl syndrome OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0237873 Physiological sexual disorders HSDN C0004134 Dyssynergia C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C1850106 Raine syndrome MalaCards C4085862 Bothered by nausea C0595812 Fistula route HSDN C3829611 Nausea frequency C0026896 Myasthenia gravis HSDN C0233514 Behavior abnormal C0270972 Cornelia de lange syndrome HPO C4085211 Pain distress question C0033941 Psychoses, substance-induced HSDN C2237041 Shox gene with short stature C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0018418 Gynecomastia HSDN C0857305 Thrombocytopenia purpura C1956346 Coronary artery disease HSDN C1557397 Adverse event associated with pain C0025037 Meckel diverticulum HSDN C0037763 Spasm C0264408 Childhood asthma UMLS C0557874 Global developmental delay C3809005 Cardiofaciocutaneous syndrome 2 MalaCards C3496180 Sleep apnea C0029454 Osteopetrosis MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037397 Behavior social HSDN C0042928 Paralysis vocal cord C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C2911645 Weight loss adverse event C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C0026826 High muscle tone C2751067 Parkinsonism-dystonia, infantile MalaCards|HPO C3887638 Failure to thrive in infant C0037466 Socioenvironmental therapy HSDN C4084775 Usual severity weight loss C0268080 Hypercalcemia, idiopathic, of infancy HPO C3641755 Have constipation C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0518090 Frequency of pain question C0038012 Spondylitis HSDN C1253937 Pericardial effusion C2931242 Familial waldmann's disease MalaCards C0043352 Absent salivary secretion C1535942 Autoimmune polyglandular syndrome type iii MalaCards C0019825 Voice hoarseness C0002950 Aneurysms inflammatory HSDN C4084768 Usual severity vomiting C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0038506 Stutter C0040369 Economy token HSDN C0040460 Dental pain C0024121 Lung neoplasms HSDN C0018520 Breath odor C0040456 Tooth impaction HSDN C0013604 Edematous C0009442 Common bile duct neoplasms HSDN C0013604 Edematous C0015645 Fasciitis HSDN C2024893 Cardiovascular surgery result: fatigue C0015300 Exophthalmos HSDN C0004604 Pain back C0020473 Hyperlipidemia HSDN C0151786 Weakness muscle C0024282 Lymphocytosis HSDN C0018784 Deafness sensorineural C2984291 Glioblastoma multiforme pathway HSDN C0497406 Over weight C2239176 Liver carcinoma HSDN C0004134 Dyssynergia C0270724 Infantile neuroaxonal dystrophy HPO|UMLS C0004134 Dyssynergia C0040053 Thrombosis HSDN C0032914 Toxemia C0455988 Hydrops fetalis, non-immune MalaCards C0019079 Bloody sputum C1336271 Stage iii small cell carcinoma of lung UMLS C0030486 Extremity paralysis, lower C0007273 Carotid artery diseases HSDN C0206160 Retic count elevated C0268202 Beta-sitosterolemia MalaCards C0024031 Back pain lower back C1962963 Osteoporosis adverse event HSDN C1963091 Diarrhea adverse event C1962983 Cataract adverse event HSDN C4084768 Usual severity vomiting C0032319 Pneumopericardium HSDN C4085552 Dry mouth C0033770 Prune belly syndrome MalaCards C4085222 Nausea C0013473 Eating disorders HSDN C0010200 Cough symptom C0006114 Cerebral edema HSDN C0030193 Sense of pain C0010034 Corneal diseases HSDN C0028738 Nystagmus C4014856 Cone-rod dystrophy 20 MalaCards C2880345 Corneal deposits in metabolic disorders, left eye C0015397 Disorder of eye UMLS C0019079 Bloody sputum C0018944 Hematoma HSDN C0013404 Respiratory difficulty C0005758 Bulla HSDN C4084774 Have weight loss C2984302 Leishmaniasis infection pathway HSDN C0460137 Push down or depress C0023788 Whipple disease OrphaNet|MalaCards C0027498 Nausea vomiting C1136033 Cutaneous mastocytosis MalaCards C0518090 Frequency of pain question C0003872 Arthritis, psoriatic HSDN C0518090 Frequency of pain question C0399526 Class iii malocclusion HSDN C0033774 Skin pruritus C0023968 Loiasis HSDN C4084802 Usual severity diarrhea C0039538 Teratoma HSDN C0015799 Feminisation C1458155 Mammary neoplasms HSDN C0004134 Dyssynergia C0035053 Spontaneous remission HSDN C1963067 Atrial fibrillation adverse event C2678476 Cardiomyopathy, dilated, 1y MalaCards C4085211 Pain distress question C0013505 Cyst, pulmonary hydatid HSDN C0009806 Constipate C3897082 Stage iva colon cancer UMLS C0013604 Edematous C0006267 Bronchiectasis HSDN C0424755 Fever symptoms C0311389 Nonspecific urethritis HSDN C0042571 Vertigo subjective C0155516 Hyperactive labyrinth-bilat. UMLS C4084802 Usual severity diarrhea C0027858 Neuroma HSDN C4084784 Diarrhea C0042076 Urologic neoplasms HSDN C0036572 Convulsion C0677838 Grief loss HSDN C0036572 Convulsion C3553929 Peroxisome biogenesis disorder 3a (zellweger) MalaCards C0018772 Deafness C0007682 Cns disorder HSDN C0231690 Staggering gait C0392702 Abnormal involuntary movement UMLS C1549543 Administration method - pain C0041960 Ureterocele HSDN C0232466 Feeding difficulty C3280479 Pitt-hopkins-like syndrome 2 MalaCards C0018991 Paralysis one side of body C0004114 Astrocytoma HSDN C0518090 Frequency of pain question C0014055 Encephalitis, epidemic HSDN C0020903 Illusion C2326002 Infradentale HSDN C0027497 Queasy C2963140 Arteriovenous fistula in use with two needles HSDN C0030193 Sense of pain C0036271 Scalp dermatoses HSDN C0424755 Fever symptoms C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C4085661 Usual severity nausea C0001175 Acquired immunodeficiency syndrome HSDN C0011991 Loose stools C0024523 Malabsorption syndrome MalaCards C0040259 Tinea pedis C2984299 Asthma pathway HSDN C1384666 Decreased hearing C2676285 Bone fragility with contractures, arterial rupture, and deafness HPO C0425791 Breast skin orange peel texture C0278601 Inflammatory breast carcinoma UMLS C0013395 Indigestion C1334809 Mucinous adenocarcinoma of stomach UMLS C3665346 Loss sight C0265301 Sclerosteosis HPO|UMLS C4085548 Usual severity dizziness C0036095 Salivary gland neoplasms HSDN C0040485 Wryneck C4023011 Abnormal craniofacial muscle tone UMLS C1549543 Administration method - pain C1963266 Uveitis adverse event HSDN C1519353 Skin eruption papular C0023645 Lichen planus follicularis OrphaNet|MalaCards C0850758 Pain pelvic C0011854 Diabetes mellitus, insulin-dependent HSDN C1557397 Adverse event associated with pain C0039786 Therapeutic communities HSDN C1963091 Diarrhea adverse event C0008073 Developmental disabilities HSDN C1836296 Lower extremity weakness C1333989 Familial meningioma MalaCards C4042891 Sleep wake disorders C0023434 Chronic lymphocytic leukemia HSDN C0005904 Alteration in body temperature C0005283 Beta thalassemia OrphaNet C0004134 Dyssynergia C0268608 Deficiency of dihydrofolate reductase MalaCards C2700617 Irritation - emotion C0393706 Early infantile epileptic encephalopathy with suppression bursts MalaCards C1963252 Tremor adverse event C0018671 Head and neck neoplasms HSDN C1971624 Appetite absent C0018018 Goat disease HSDN C1963274 Vasculitis adverse event C2936664 Acquired hypogammaglobulinemia MalaCards C2984057 Have nausea C1962963 Osteoporosis adverse event HSDN C0026821 Cramp C0019693 Hiv infections HSDN C0026826 High muscle tone C0796272 Brooks syndrome MalaCards C2911647 Weight gain adverse event C0005604 Trauma birth HSDN C0030552 Paralysis partial C0006147 Breast fed HSDN C0030554 Abnormal sensation C0033817 Pseudomonas infections HSDN C0011570 Monopolar depression C1864112 Huntington disease-like 1 MalaCards|HPO C3463815 Feel fatigue C1145628 Autonomic nervous system disorders HSDN C0011991 Loose stools C0272129 Donath-landsteiner hemolytic anemia MalaCards C0019572 Hairiness C0010709 Cyst HSDN C4084774 Have weight loss C0266836 Infantile colic HSDN C1962972 Proteinuria adverse event C0023473 Myeloid leukemia, chronic HSDN C0010200 Cough symptom C0037930 Spinal cord neoplasms HSDN C0003862 Pain joint C0043352 Xerostomia HSDN C0011991 Loose stools C1836330 Erythrokeratodermia variabilis 3 (disorder) HPO|UMLS C0522224 Palsied C0002395 Alzheimer's disease HSDN C0020673 Hypothermia (central) (local) C1623041 Breast-fed HSDN C2024878 Cardiovascular surgery result: dyspnea C0005891 Bodies image HSDN C0727671 Red cross toothache drops C0011351 Dental enamel hypoplasia HSDN C4085317 Diarrhea frequency C0040948 Trichostrongyliasis HSDN C1549543 Administration method - pain C0032290 Aspiration pneumonia HSDN C4084724 Usual severity constipation C1963083 Cholecystitis adverse event HSDN C3541349 Syncope C0040761 Transposition of great vessels HSDN C0042798 Vision dim C0033788 Pseudo-hurler polydystrophy OrphaNet|MalaCards C0015672 Decreased energy C0026857 Musculoskeletal diseases HSDN C0349588 Stature short C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0024116 Lung diseases, fungal HSDN C1963281 Vomiting adverse event C0342443 Adrenal cushing's syndrome HSDN C3641756 Have diarrhea C0027932 Neurotic disorders HSDN C0917816 Deficiency mental C4015323 Leukodystrophy, hypomyelinating, 9 MalaCards C0031256 Petechia C0543697 Mixed cryoglobulinemia OrphaNet|MalaCards C0015672 Decreased energy C0023479 Acute myelomonocytic leukemia UMLS C0040034 Thrombocytopenia C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C4084768 Usual severity vomiting C0012691 Dislocations HSDN C0040485 Wryneck C0004364 Autoimmune diseases HSDN C0018777 Deafness, conductive C1876185 Dysgnathia complex MalaCards|HPO C4084767 Bothered by vomiting C0085094 Head injury closed HSDN C3146279 Coma C0037274 Dermatologic disorders HSDN C3274924 Have been coughing C0014869 Peptic esophagitis HSDN C4085211 Pain distress question C0039730 Thalassemia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1704436 Peripheral arterial diseases HSDN C0015230 Exanthem C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C4084802 Usual severity diarrhea C0010038 Corneal opacity HSDN C4084784 Diarrhea C0221036 Acrodermatitis enteropathica HPO C0015970 Fever unknown origin C0012813 Diverticulitis HSDN C1963063 Anorexia adverse event C0003873 Rheumatoid arthritis HSDN C1069915 Vertigo C0022738 Klippel-feil syndrome HSDN C1963091 Diarrhea adverse event C0206692 Carcinoma, lobular HSDN C0011991 Loose stools C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C2911645 Weight loss adverse event C2931894 Mucolipidosis 2 MalaCards|HPO C3641756 Have diarrhea C0022758 Kap HSDN C2203646 Jaundice C0342191 Familial dyshormonogenetic goiter MalaCards C0015230 Exanthem C0348980 Measles complic by meningitis UMLS C1963170 Hypothermia adverse event C0012979 Canine disease HSDN C0038002 Spleen enlargement C0268060 Juvenile hemochromatosis MalaCards C0018772 Deafness C0019195 Hepatitis, viral, human HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C3541349 Syncope C0155843 Retropharyngeal abscess HSDN C4084802 Usual severity diarrhea C0018889 Helminthiasis HSDN C0812426 Kidney problem C0266294 Unilateral agenesis of kidney UMLS C0018989 Paresis of one side of body C0013362 Dysarthria UMLS C4084774 Have weight loss C0262627 Seroma HSDN C0015468 Face pain C0011853 Diabetes mellitus, experimental HSDN C0007758 Cerebellar ataxia C2936862 Bardet-biedl syndrome 1 (disorder) MalaCards C0015230 Exanthem C0040100 Thymoma MalaCards C4084768 Usual severity vomiting C0079744 Diffuse large b-cell lymphoma HSDN C0020903 Illusion C1962983 Cataract adverse event HSDN C0018772 Deafness C3554163 Deafness, autosomal recessive 18b MalaCards C3541349 Syncope C0270611 Brain damage HSDN C2242996 Tingling C0458219 Complex regional pain syndromes HSDN C0018784 Deafness sensorineural C0027743 Nerve compression syndrome HSDN C2203646 Jaundice C0017636 Glioblastoma HSDN C4084776 Weight loss C0279607 Adult primary hepatocellular carcinoma MalaCards C2029884 Hearing loss by exam C0024141 Lupus erythematosus, systemic HSDN C1510456 Wernicke aphasia C0497327 Dementia HSDN C0009676 Confusion state C0025290 Aseptic meningitis HSDN C3665347 Vision impaired C1847024 Albinism, oculocutaneous, type ib (disorder) OrphaNet|HPO|MalaCards C0002962 Angina C1959582 Pten hamartoma tumor syndrome MalaCards C0270948 Neurogenic muscular atrophy C0410203 X-linked centronuclear myopathy OrphaNet|HPO C1549543 Administration method - pain C0028796 Dermatitis, occupational HSDN C3539023 Pelvic pain increasing in frequency C1961100 Erectile dysfunction adverse event HSDN C0221161 Breathing shallow C2677109 Leukodystrophy, hypomyelinating, 4 MalaCards|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0020626 Hypoparathyroidism HSDN C0013362 Dysarthrias C3148763 Muscular dystrophy, limb-girdle, type 1e MalaCards C3887638 Failure to thrive in infant C0266526 Norrie disease MalaCards|HPO C4042891 Sleep wake disorders C0022104 Irritable bowel syndrome HSDN C0042928 Paralysis vocal cord C0016542 Foreign body HSDN C3539889 Pelvic pain increasing in severity C1394494 Cystocele, unspecified HSDN C3829611 Nausea frequency C0037744 Perceptual spatial orientation HSDN C4084723 Constipation C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0009324 Ulcerative colitis HSDN C0039070 Collapse fleeting C0041948 Uremia HSDN C0162298 Stiffness joints C0266833 Visceral myopathy, familial MalaCards|HPO C0812426 Kidney problem C0748301 Renal failure chronic diabetes UMLS C3815497 Cough C0024788 Green monkey virus disease OrphaNet|MalaCards C0022346 Yellow skin C0002874 Aplastic anemia HSDN C1963091 Diarrhea adverse event C0027121 Myositis HSDN C0004134 Dyssynergia C0027877 Neuronal ceroid-lipofuscinoses MalaCards C1145670 Failure respiratory C2931902 Acute brachial neuritis MalaCards C0016382 Cutaneous vascular engorgement C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C2984057 Have nausea C0024305 Lymphoma, non-hodgkin HSDN C0035078 Failure kidney C0268448 Primary hypomagnesemia (disorder) MalaCards C0007758 Cerebellar ataxia C0002736 Amyotrophic lateral sclerosis HSDN C1549543 Administration method - pain C0000810 Incomplete spontaneous abortion HSDN C4084723 Constipation C0027651 Tumor HSDN C0040485 Wryneck C0015458 Facial hemiatrophy HSDN C0522224 Palsied C3489413 Lipomatosis, multiple HSDN C0002622 Amnesias C0751865 Alcohol-induced disorders, nervous system HSDN C4084725 Usual severity cough C2586211 Thrombosis of blood vessel HSDN C0233565 Bradykinesia C1846862 Parkinson disease 8 (disorder) UMLS C4085222 Nausea C0002940 Aneurysm HSDN C2032395 Pelvic pain on the left C0243001 Abdominal abscess HSDN C0270777 Cord edema spinal C0474991 Edema of cervical cord UMLS C0497247 Blood pressure elevation C0281479 Primary systemic amyloidosis MalaCards C3539890 Pelvic pain causes awakening at night C0017181 Gastrointestinal hemorrhage HSDN C0027497 Queasy C1837218 Cleft palate, isolated HSDN C3146279 Coma C1855116 Methylmalonic aciduria, mut(-) type HPO C0398650 Idiopathic thrombocytopenia purpura C0032001 Pituitary apoplexy HSDN C4084784 Diarrhea C0007117 Basal cell carcinoma HSDN C4085642 Level of joint stiffness C1862472 Oculomelic amyoplasia OrphaNet|HPO|MalaCards C0036572 Convulsion C0268242 Niemann-pick disease, type a MalaCards C4084767 Bothered by vomiting C1555914 Psychologist - psychotherapy, group HSDN C4084774 Have weight loss C0017638 Glioma HSDN C0018772 Deafness C0010964 Dandy-walker syndrome HSDN C0745977 Lower leg swelling C0740728 Lower extremity problem UMLS C0522224 Palsied C0018809 Heart neoplasm HSDN C2911645 Weight loss adverse event C0040100 Thymoma HSDN C0042023 Urination frequency C3178970 Entrapment, pudendal nerve MalaCards C0040485 Wryneck C0344315 Depressed mood HSDN C0151686 Growth retardation C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards C4082202 Sleep quality question C0006035 Borrelia infections MalaCards C4084773 Bothered by weight gain C0040411 Tongue neoplasms HSDN C0042798 Vision dim C0393665 Multiple sclerosis, chronic progressive HSDN C0151786 Weakness muscle C0751871 Autoimmune diseases of the nervous system HSDN C0003862 Pain joint C0085433 Acquired joint deformities HSDN C4085222 Nausea C1962983 Cataract adverse event HSDN C0349588 Stature short C0796142 Sao paulo mca-mr syndrome MalaCards C0018965 Blood urine C2347126 Microscopic polyarteritis MalaCards C0271215 Blindness legal C0030804 Pemphigoid, benign mucous membrane MalaCards C0026838 Spasticity muscle C1962958 Hematoma adverse event HSDN C0022346 Yellow skin C0007784 Cerebral hemisphere hemorrhage HSDN C3887638 Failure to thrive in infant C0265965 Dyskeratosis congenita MalaCards C0030552 Paralysis partial C0085111 Ankle injury HSDN C0030554 Abnormal sensation C0007222 Cardiovascular diseases HSDN C1279888 Proteinuria of undiagnosed cause C0038525 Subarachnoid hemorrhage HSDN C0037383 Sneeze C0036969 Pasteurellosis, pneumonic HSDN C4084726 Distress cough C0001721 Emotional affect HSDN C4085211 Pain distress question C0747533 Peroneal neuropathy HSDN C0042963 Symptoms vomiting C0001125 Acidosis, lactic HSDN C1963170 Hypothermia adverse event C0036690 Septicemia HSDN C0522224 Palsied C0003615 Appendicitis HSDN C0413252 Hypothermia due to exposure C0008354 Cholera HSDN C1963180 Neck pain adverse event C0014474 Ependymoma HSDN C0036572 Convulsion C0729544 Fungal cns infection HSDN C0030193 Sense of pain C1704326 Role - roleclass HSDN C4085317 Diarrhea frequency C2945560 Hemolytic HSDN C0575081 Abnormal gait C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0017150 Gastrinoma OrphaNet|MalaCards C0011991 Loose stools C0600104 Obsessive compulsive behavior HSDN C0035078 Failure kidney C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0011991 Loose stools C0004782 Basal ganglia diseases HSDN C0042571 Vertigo subjective C0030581 Parotid neoplasms HSDN C0015402 Hemorrhage eye C0043167 Pertussis HSDN C0018681 Headache, cephalalgia C0036472 Scrub typhus DiseaseOntology|OrphaNet|MalaCards C0035078 Failure kidney C0038325 Stevens-johnson syndrome HPO C4085211 Pain distress question C0699744 Infection of ear HSDN C0019079 Bloody sputum C0020538 Hypertensive disease HSDN C0020305 Fetal edema C2936830 Chromosome 13 duplication OrphaNet|MalaCards C0851578 Disorder sleep C3180937 15q11.2 microdeletion MalaCards C1963249 Tinnitus adverse event C0206719 Central neurocytoma MalaCards C0036572 Convulsion C0011884 Diabetic retinopathy HSDN C0013456 Pain ear C0023051 Laryngeal diseases HSDN C0233844 Awkwardness C0085209 Bovine spongiform encephalitis MalaCards C1549543 Administration method - pain C0041318 Tuberculosis, meningeal HSDN C1963065 Apnea adverse event C0040583 Tracheal stenosis HSDN C2024893 Cardiovascular surgery result: fatigue C0018273 Growth disorders HSDN C0007758 Cerebellar ataxia C0015310 Exotropia HSDN C0344315 Mood depressed C0393590 Fahr's syndrome (disorder) MalaCards|HPO C4042891 Sleep wake disorders C0236733 Amphetamine-related disorders HSDN C2237041 Shox gene with short stature C0265339 Borjeson-forssman-lehmann syndrome MalaCards|HPO C0035229 Respiratory function impaired C0220726 Diastrophic dysplasia OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0677838 Grief loss HSDN C0349588 Stature short C1956147 Microlissencephaly MalaCards C2132198 Abnormal blistering of the skin C1846142 Hoyeraal-hreidarsson syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0015456 Facial dermatoses HSDN C1384666 Decreased hearing C0460137 Push down or depress HSDN C2237041 Shox gene with short stature C0796099 Cleft lip-palate with abnormal thumbs and microcephaly MalaCards C0812426 Kidney problem C0744421 Immune-complex glomerulonephritis UMLS C0030193 Sense of pain C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C4084725 Usual severity cough C0950123 Inborn genetic disease HSDN C0023530 Leukopenia C1304456 Congo hemorrhagic fever MalaCards C4084784 Diarrhea C0029342 Orthomyxoviridae infections HSDN C4085317 Diarrhea frequency C0026640 Mouth neoplasms HSDN C0035021 Fever, famine C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency MalaCards C0038002 Spleen enlargement C0795969 Cholestasis-pigmentary retinopathy-cleft palate syndrome MalaCards C0278152 Hemifacial spasms C0024796 Marfan syndrome HSDN C4084767 Bothered by vomiting C0022650 Kidney calculi HSDN C1962972 Proteinuria adverse event C0403443 Renal failure, progressive, with hypertension MalaCards C0162298 Stiffness joints C1849929 Pfeiffer palm teller syndrome MalaCards C0018681 Headache, cephalalgia C1332961 Childhood cerebral diffuse astrocytoma UMLS C3641756 Have diarrhea C1866495 Bartter syndrome, antenatal type 1 HPO C0917816 Deficiency mental C1841696 Macdermot patton williams syndrome MalaCards C0151786 Weakness muscle C0011989 Camurati-engelmann syndrome OrphaNet|HSDN|HPO|MalaCards C0030193 Sense of pain C1273017 Tibial adamantinoma UMLS C0026821 Cramp C1850718 Myopathy with exercise intolerance, swedish type MalaCards|HPO|UMLS C1962972 Proteinuria adverse event C0003962 Ascites HSDN C4085862 Bothered by nausea C0008925 Cleft palate HSDN C2919142 Short stature adverse event C0018036 Hypertension, goldblatt OrphaNet C0011991 Loose stools C0038941 Incisional infection HSDN C0009421 Comatose C0038579 Substance abuse, intravenous HSDN C0020615 Hypoglycemia nos C1859995 Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency HPO C1963077 Bone pain adverse event C0206624 Hepatoblastoma MalaCards C0426579 Anorexia symptom C1263846 Attention deficit hyperactivity disorder HSDN C0030552 Paralysis partial C1621958 Glioblastoma multiforme MalaCards C3539891 Pelvic pain to the rear C0017181 Gastrointestinal hemorrhage HSDN C2984058 Have pain C0018889 Helminthiasis HSDN C0002170 Alopecia disorders C0085860 Autoimmune syndrome type ii, polyglandular OrphaNet|MalaCards C4085222 Nausea C0022951 Lactose intolerance HSDN C1963077 Bone pain adverse event C0432292 Familial expansile osteolysis HPO C3665492 Pigmentations C0008521 Choroid diseases MalaCards C0009806 Constipate C1838568 Sacral defect and anterior sacral meningocele HPO C0038990 Sweats C0878675 Erdheim-chester disease OrphaNet|MalaCards C4085222 Nausea C1411077 Ragpicker's disease MalaCards C1557397 Adverse event associated with pain C0085392 Bacteroidaceae infection HSDN C0162298 Stiffness joints C1850568 Nakajo syndrome MalaCards C0497406 Over weight C0042338 Herpesvirus 3, human HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0022650 Kidney calculi HSDN C1549543 Administration method - pain C0010267 Cranial nerve neoplasms HSDN C0008031 Pain chest C0020676 Hypothyroidism HSDN C0518090 Frequency of pain question C0002886 Anemia, macrocytic HSDN C4084768 Usual severity vomiting C0043254 Injuries penetrating HSDN C0021359 Infertility C1855859 Hypogonadism-cataract syndrome MalaCards C0037763 Spasm C0585442 Osteosarcoma of bone HSDN C0151686 Growth retardation C1418533 Phka2 gene HPO C0023014 Developmental disorder language C0023529 Leukomalacia, periventricular HSDN C4084727 Cough frequency C0549143 Pulmonary renal syndrome MalaCards C4084723 Constipation C0268386 Amyloid polyneuropathy, swiss type MalaCards C0151889 Reflexes tendon increased C0002736 Amyotrophic lateral sclerosis MalaCards C0027497 Queasy C0026896 Myasthenia gravis HSDN C4084767 Bothered by vomiting C0020621 Hypokalemia HSDN C0024031 Back pain lower back C2911643 Encounter due to family history of osteoporosis HSDN C2237041 Shox gene with short stature C1414025 Dgcr gene HPO C0424755 Fever symptoms C0040185 Tibia fracture HSDN C0497406 Over weight C0008626 Congenital chromosomal disease HSDN C0016199 Pain flank C0279702 Conventional (clear cell) renal cell carcinoma UMLS C4084802 Usual severity diarrhea C0018621 Hay fever HSDN C0030193 Sense of pain C0205930 Algoneurodystrophy UMLS C0027796 Neuralgias C0008325 Cholecystitis HSDN C0242936 Center pain C0034040 Puerperal disorders HSDN C0018524 Hallucinate C1963198 Pancreatitis adverse event HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1299624 Postural orthostatic tachycardia syndrome HSDN C0151786 Weakness muscle C0033873 Psychiatry HSDN C0035229 Respiratory function impaired C0019101 Hemorrhagic fever with renal syndrome OrphaNet|MalaCards C0018926 Emesis bloody C0007222 Cardiovascular diseases HSDN C0015672 Decreased energy C0039483 Giant cell arteritis OrphaNet|HSDN|HPO|MalaCards C0004134 Dyssynergia C0011854 Diabetes mellitus, insulin-dependent HSDN C4084802 Usual severity diarrhea C1801959 Histiocytic medullary reticulosis (disorder) MalaCards|HPO C2984058 Have pain C0041408 Turner syndrome HSDN C3887638 Failure to thrive in infant C1833104 Diabetes mellitus, permanent neonatal OrphaNet|HPO|MalaCards C0007642 Cellulitis nos C3489795 Hyper-ige recurrent infection syndrome, autosomal dominant HPO C0349588 Stature short C3151218 Osteogenesis imperfecta, type xi MalaCards|HPO C0020305 Fetal edema C0023569 Levocardia HSDN C2911647 Weight gain adverse event C0026896 Myasthenia gravis HSDN C0028738 Nystagmus C0024814 Marinesco-sjogren syndrome MalaCards|HPO C0020673 Hypothermia (central) (local) C0023441 Leukemia, experimental HSDN C0000727 Abdomen acute C0006109 Brain damage, chronic HSDN C1557397 Adverse event associated with pain C0020433 Hyperbilirubinemia HSDN C0000727 Abdomen acute C0035358 Retroperitoneal neoplasm HSDN C4085211 Pain distress question C0025286 Meningioma HSDN C0019079 Bloody sputum C0032310 Pneumonia, viral HSDN C0024032 Birth weight subnormal C0010314 Cri-du-chat syndrome MalaCards C1962972 Proteinuria adverse event C0037274 Dermatologic disorders HSDN C0232493 Epigastric pain C0279607 Adult primary hepatocellular carcinoma MalaCards C0015469 Facial paralysis C0006145 Breast diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1696469 Shin splints HSDN C1963249 Tinnitus adverse event C0043251 Wounds and injuries HSDN C0427055 Face weakness C0432262 Dysosteosclerosis MalaCards C3641756 Have diarrhea C0038459 Equine strongyle infection HSDN C0039070 Collapse fleeting C2609414 Acute kidney injury HSDN C0018989 Paresis of one side of body C0856636 Hemiparesis transient UMLS C0278152 Hemifacial spasms C1334698 Meningothelial cell neoplasm MalaCards C0003811 Cardiac rhythm disturbance C2749346 Refsum disease, adult, 2 HPO C1279888 Proteinuria of undiagnosed cause C0009450 Disease caused by microorganism HSDN C2203646 Jaundice C2930674 Babesioses, human MalaCards C0015672 Decreased energy C0039504 Injuries tendon HSDN C0860603 Anxiety symptom C0342200 Endemic cretinism MalaCards C0011991 Loose stools C0042063 Urogenital abnormalities HSDN C0015230 Exanthem C1274329 Exanthema subitum due to human herpesvirus 7 UMLS C0151603 Edema generalized C0085083 Ovarian hyperstimulation syndrome MalaCards|HPO C3641756 Have diarrhea C0341299 Collagenous sprue HSDN C3463815 Feel fatigue C0038661 Suicide HSDN C0015672 Decreased energy C0036864 Sexual relations HSDN C1963065 Apnea adverse event C0020625 Hyponatremia HSDN C3146279 Coma C0023890 Liver cirrhosis HSDN C1608971 Optic nerve pallor C1836861 Fanconi anemia, complementation group i MalaCards C0000737 Abdomen pain C1336456 Stage i hepatocellular carcinoma UMLS C4085211 Pain distress question C0002886 Anemia, macrocytic HSDN C1963180 Neck pain adverse event C0022758 Kap HSDN C0020673 Hypothermia (central) (local) C0002395 Alzheimer's disease HSDN C1962972 Proteinuria adverse event C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C0344428 Ventricular tachycardia by ecg finding C2678476 Cardiomyopathy, dilated, 1y MalaCards|HPO C4084776 Weight loss C1856243 Growth factors, combined defect of OrphaNet|MalaCards C4085549 Dizziness C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C0424755 Fever symptoms C0034530 Injury radiation HSDN C0231528 Muscle pain generalized C0030328 Panniculitis, nodular nonsuppurative OrphaNet|MalaCards C0239574 Fever low grade C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C4085222 Nausea C3838758 Familial hyperaldosteronism type 3 MalaCards C0014089 Functional encopresis C0034882 Rectal diseases HSDN C4084788 Have dizziness C0002351 Altitude sickness HSDN C4085317 Diarrhea frequency C1865643 Cholestasis, progressive familial intrahepatic 3 HPO C4084774 Have weight loss C0018889 Helminthiasis HSDN C0042963 Symptoms vomiting C0035305 Retinal detachment HSDN C0917816 Deficiency mental C2930953 Halal setton wang syndrome OrphaNet|MalaCards C3539892 Pelvic pain in front C0009450 Disease caused by microorganism HSDN C0030554 Abnormal sensation C0334533 Arteriovenous hemangioma HSDN C2315100 Pediatric failure to thrive C1850406 Navajo neurohepatopathy MalaCards|HPO C0009398 Color vision defects C1843815 Newfoundland rod-cone dystrophy MalaCards|HPO C0007758 Cerebellar ataxia C1720189 Episodic ataxia UMLS C0019572 Hairiness C0917715 Hajdu-cheney syndrome MalaCards|HPO C0522224 Palsied C0027441 Nasopharyngitis HSDN C2984058 Have pain C0085166 Bacterial vaginosis HSDN C4084776 Weight loss C2242703 Cardio-renal syndrome HSDN C3641755 Have constipation C1578691 Congenital myxedema MalaCards C0262527 Intermittent abdominal pain C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C1962972 Proteinuria adverse event C0002985 Angiokeratoma HSDN C1961131 Cough adverse event C0036202 Sarcoidosis OrphaNet|HSDN|HPO|MalaCards C0232943 Metromenorrhagia C2979982 Vaginal hemorrhage UMLS C0742292 Chest pain char typical C0002965 Angina, unstable UMLS C0009421 Comatose C1863844 Adult-onset citrullinemia type 2 HPO C0086565 Liver function abnormal C0038325 Stevens-johnson syndrome HPO C0022346 Yellow skin C0005283 Beta thalassemia HSDN C1963091 Diarrhea adverse event C0013364 Dysautonomia, familial HPO C0027066 Myoclonic jerking C0333641 Atrophic HSDN C3665492 Pigmentations C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0026838 Spasticity muscle C0003507 Aortic valve stenosis HSDN C0576456 Poor feeding C1845862 Creatine deficiency, x-linked MalaCards C0012833 Dizzy C0035309 Retinal diseases HSDN C0000737 Abdomen pain C0026266 Mitral valve insufficiency HSDN C0023530 Leukopenia C1856796 Estren-dameshek variant of fanconi anemia HPO C0004310 Auditory disorder process C0751955 Brain infarction HSDN C0036659 Sensation disorder C0032962 Pregnancy complications HSDN C0015732 Feces incontinence C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C0042571 Vertigo subjective C0018798 Congenital heart defects HSDN C0030486 Extremity paralysis, lower C0024228 Lymphatic diseases HSDN C0042024 Urine incontinence C0031154 Peritonitis HSDN C0030193 Sense of pain C0149875 Primary dysmenorrhea UMLS C2024893 Cardiovascular surgery result: fatigue C0153653 Malignant tumor of parathyroid gland MalaCards C0040822 D tremors C2026458 Cerebral degenerations, extrapyramidal and movement disorders UMLS C0039231 Heartbeats increased C1861457 Progressive encephalomyelitis with rigidity MalaCards C3641756 Have diarrhea C0032963 Pregnancy complications, cardiovascular HSDN C0332573 Macula C0855015 Stage i acral lentiginous melanoma UMLS C0332573 Macula C0263343 Urticaria pigmentosa, multiple nodules or plaques UMLS C4084767 Bothered by vomiting C1838979 Mitochondrial complex i deficiency MalaCards|HPO C0027497 Queasy C1000483 Genus anemia HSDN C0042420 Vasovagal episode C0344434 Atrial fibrillation ecg HSDN C0042024 Urine incontinence C1457883 Aggressive reaction HSDN C4084775 Usual severity weight loss C0019061 Hemolytic-uremic syndrome HSDN C1384666 Decreased hearing C1866927 Smcr HPO C0242936 Center pain C0002895 Anemia, sickle cell OrphaNet|MalaCards C1557397 Adverse event associated with pain C0007798 Cerebral ventricle neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0750394 Wbc low HSDN C0917816 Deficiency mental C0029454 Osteopetrosis MalaCards C0522224 Palsied C0019699 Hiv seropositivity HSDN C1557397 Adverse event associated with pain C0008049 Chicken pox HSDN C0151786 Weakness muscle C0344315 Depressed mood HSDN C2029884 Hearing loss by exam C0027666 Neoplasms, radiation-induced HSDN C2919142 Short stature adverse event C2675897 1q21.1 contiguous gene deletion OrphaNet|MalaCards C4084776 Weight loss C0018889 Helminthiasis HSDN C0242936 Center pain C1366535 Avp gene HSDN C0042963 Symptoms vomiting C0023896 Alcoholic liver diseases UMLS C2024878 Cardiovascular surgery result: dyspnea C1848814 Thymoma, familial MalaCards C0151827 Pain eye C2020541 Strabismus HSDN C0232943 Metromenorrhagia C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C0030193 Sense of pain C1367554 Adamantinoma UMLS C4085210 Usual severity pain C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C2032395 Pelvic pain on the left C0001418 Adenocarcinoma HSDN C4084769 Vomiting frequency C0006434 Burn injury HSDN C4084723 Constipation C1847319 Paraganglioma and gastric stromal sarcoma MalaCards C1456822 Lower extremity pain walking C1859372 Calcification of joints and arteries MalaCards C1963184 Nystagmus adverse event C0520719 Spinopontine atrophy MalaCards C0028738 Nystagmus C0796272 Brooks syndrome MalaCards C3815497 Cough C0019069 Hemophilia a HSDN C0917816 Deficiency mental C1855923 Hyperphosphatasia with mental retardation MalaCards|HPO C2237041 Shox gene with short stature C1563705 Nephrogenic diabetes insipidus, type i HPO C0860603 Anxiety symptom C0033800 Pseudoglioma MalaCards C0011991 Loose stools C0243026 Sepsis UMLS C0003469 Anxiety disorder C0221033 Trisomy x syndrome MalaCards C3146279 Coma C3812171 Bradycardia by ecg finding HSDN C1971624 Appetite absent C0268412 Infantile hypophosphatasia MalaCards|HPO C0151889 Reflexes tendon increased C0796204 Worster-drought syndrome OrphaNet|MalaCards C0018834 Brash C3542499 Aminoacylase 2 deficiency OrphaNet|MalaCards C0000737 Abdomen pain C0010074 Coronary vessel anomalies HSDN C3539889 Pelvic pain increasing in severity C0042029 Urinary tract infection HSDN C0344434 Atrial fibrillation ecg C3553409 Cardiomyopathy, dilated, 2b MalaCards C2984058 Have pain C1963068 Atrial flutter adverse event HSDN C0013404 Respiratory difficulty C0011168 Deglutition disorders UMLS C0030552 Paralysis partial C0002880 Autoimmune hemolytic anemia OrphaNet C0030486 Extremity paralysis, lower C0002726 Amyloidosis HSDN C4084802 Usual severity diarrhea C0275524 Coinfection HSDN C2024893 Cardiovascular surgery result: fatigue C1837218 Cleft palate, isolated HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1366535 Avp gene HSDN C0018772 Deafness C0023264 Leigh disease HSDN C0013404 Respiratory difficulty C0004623 Bacterial infections HSDN C1384666 Decreased hearing C0270972 Cornelia de lange syndrome HSDN C1069915 Vertigo C1963229 Retinal detachment adverse event HSDN C0085632 Listlessness C1843891 Spinocerebellar ataxia 21 HPO|UMLS C0042024 Urine incontinence C0006434 Burn injury HSDN C4049602 Hyperactivity C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0000727 Abdomen acute C0042384 Vasculitis HSDN C2984057 Have nausea C0220847 C hepatitis virus HSDN C0424755 Fever symptoms C0030567 Parkinson disease HSDN C0035078 Failure kidney C0020579 Hypervitaminosis a MalaCards C0030193 Sense of pain C0009782 Connective tissue diseases HSDN C1549543 Administration method - pain C0037322 Active eye movement sleep HSDN C0522224 Palsied C0038587 Substance withdrawal syndrome HSDN C3641755 Have constipation C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0015672 Decreased energy C2073625 X-ray of chest: pleural effusion HSDN C0151786 Weakness muscle C1260386 Glucocorticoid-remediable aldosteronism HPO C3541349 Syncope C3814778 Hemolytic index HSDN C3898969 Have been vomiting C0020541 Hypertension, portal HSDN C4084776 Weight loss C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C3641756 Have diarrhea C0024117 Chronic obstructive airway disease HSDN C0476273 Distress respiratory C0349663 Immature malignant teratoma of mediastinum UMLS C0700078 Deep tendon reflex decrease C0221759 Brachial plexus neuritis MalaCards C1549543 Administration method - pain C0752140 Intracranial embolism HSDN C0017181 Gastrointestinal bleed C0085655 Polymyositis MalaCards C0002962 Angina C0023267 Fibroid tumor HSDN C0021359 Infertility C1865614 Hemochromatosis, type 2a MalaCards C0013362 Dysarthrias C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C0012833 Dizzy C1881674 Medical device emits smoke HSDN C0015672 Decreased energy C0009763 Conjunctivitis HSDN C4084784 Diarrhea C0162869 Aneurysm, ruptured HSDN C2911645 Weight loss adverse event C0022134 Islet cell adenoma HSDN C3641755 Have constipation C0001403 Addison disease OrphaNet C0002962 Angina C0016663 Pathological fracture HSDN C0231341 Aging premature C0085215 Ovarian failure, premature HSDN C0557874 Global developmental delay C1135161 Stage 4s neuroblastoma MalaCards C2700617 Irritation - emotion C3887678 Cpnet MalaCards C0349588 Stature short C0001768 Agammaglobulinemia MalaCards C1279888 Proteinuria of undiagnosed cause C0011071 Sudden death HSDN C2128817 Single skin crust C0346153 Breast cancer, familial MalaCards C1962972 Proteinuria adverse event C1845285 Martin-probst deafness-mental retardation syndrome MalaCards C3539020 Pelvic pain decreasing in frequency C0026857 Musculoskeletal diseases HSDN C1963087 Constipation adverse event C0338503 Septo-optic dysplasia HPO C0151889 Reflexes tendon increased C2931667 Fitzsimmons walson mellor syndrome MalaCards C0851578 Disorder sleep C0038273 Stereotypic movement disorder HSDN C0008031 Pain chest C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C3815497 Cough C0007194 Hypertrophic cardiomyopathy HSDN C3887638 Failure to thrive in infant C1855102 Methylmalonic aciduria cblb type HPO C0424755 Fever symptoms C0008049 Chicken pox DiseaseOntology|HSDN|MalaCards C0015938 Fetal macrosomia C0032787 Postoperative complications HSDN C0036396 Sciatica C0936248 Chondroma HSDN C0020673 Hypothermia (central) (local) C0011882 Diabetic neuropathies HSDN C0000737 Abdomen pain C3897528 Stage iiib rectal cancer UMLS C0036572 Convulsion C0220765 Weaver-like syndrome MalaCards|HPO C0349588 Stature short C2931811 Chromosome 18, trisomy 18p MalaCards C0040485 Wryneck C0040124 Thyroglossal duct cyst HSDN C4084784 Diarrhea C0040954 Infection by trichuris trichiura DiseaseOntology|MalaCards C0042928 Paralysis vocal cord C0027813 Neuritis HSDN C0271215 Blindness legal C0398621 Hypoplasminogenemia MalaCards C0013404 Respiratory difficulty C0003496 Aortic rupture HSDN C1963091 Diarrhea adverse event C0007194 Hypertrophic cardiomyopathy HSDN C2237041 Shox gene with short stature C2931547 Kozlowski-krajewska syndrome OrphaNet|MalaCards C0013604 Edematous C0020492 Hyperostosis HSDN C4085210 Usual severity pain C0032984 Pregnancy, abdominal HSDN C0030193 Sense of pain C0016236 Flicker fusion HSDN C0086565 Liver function abnormal C1510460 Orofaciodigital syndrome i MalaCards|HPO C0011991 Loose stools C1385938 Acanthocephaliasis MalaCards C0007758 Cerebellar ataxia C3888317 Sialidosis, type 2 OrphaNet C3665347 Vision impaired C0023931 Lobstein's disease OrphaNet C2024893 Cardiovascular surgery result: fatigue C0243026 Sepsis HSDN C0013604 Edematous C0027962 Melanocytic nevus HSDN C0036572 Convulsion C0011854 Diabetes mellitus, insulin-dependent UMLS C3146279 Coma C0026266 Mitral valve insufficiency HSDN C3714552 Strength decreased C0162565 Acute intermittent porphyria MalaCards|UMLS C4084784 Diarrhea C0042880 Vitamin k deficiency HSDN C0424755 Fever symptoms C0020473 Hyperlipidemia HSDN C0007859 Pain neck C0206734 Hemangioblastoma HSDN C0349588 Stature short C1838280 Epiphyseal dysplasia, multiple, 1 MalaCards C0027497 Queasy C1333308 Carcinoma of distal biliary tract UMLS C4084802 Usual severity diarrhea C0031212 Personality disorders HSDN C0018784 Deafness sensorineural C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0851578 Disorder sleep C0010346 Crohn disease HSDN C0042571 Vertigo subjective C2973725 Pulmonary arterial hypertension OrphaNet C2024893 Cardiovascular surgery result: fatigue C0035335 Retinoblastoma HSDN C0015402 Hemorrhage eye C0043168 Whooping cough due to unspecified organism HSDN C0042963 Symptoms vomiting C2987190 Pancreatic intraductal tubulopapillary neoplasm with an associated invasive carcinoma UMLS C3463815 Feel fatigue C0039240 Supraventricular tachycardia HSDN C0233565 Bradykinesia C0007965 Chediak-higashi syndrome MalaCards|HPO C0341865 Headaches menopausal C0404559 Perimenopausal disorder UMLS C4084802 Usual severity diarrhea C3280314 Combined malonic and methylmalonic aciduria MalaCards C2911645 Weight loss adverse event C0008370 Cholestasis HSDN C0151825 Ostalgia C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0268576 Hyperleucinemia OrphaNet C3539895 Pelvic pain occurs with bowel movement C0007867 Cervix diseases HSDN C0007758 Cerebellar ataxia C0008049 Chicken pox HSDN C0028738 Nystagmus C3150674 Chromosome 15q24 deletion syndrome MalaCards|HPO C0036572 Convulsion C0752322 Epilepsy, partial, sensory HSDN C0018681 Headache, cephalalgia C0018790 Cardiac arrest HSDN C0237326 Defecation pain C1836544 Schindler disease, type i MalaCards C0018772 Deafness C3554518 Cowden syndrome 5 MalaCards C0000737 Abdomen pain C0025162 Megacolon toxic HSDN C0022408 Disorder joint C0856830 Calcium pyrophosphate arthropathy MalaCards|HPO C0042798 Vision dim C1833798 Optic nerve aplasia, bilateral HPO C4085661 Usual severity nausea C0020542 Pulmonary hypertension HSDN C4084776 Weight loss C0016978 Gallbladder neoplasm HSDN C0278152 Hemifacial spasms C0007772 Intracranial arteriovenous malformation HSDN C0600142 Flash hot C0004936 Mental disorders HSDN C4085661 Usual severity nausea C0013990 Pathological accumulation of air in tissues HSDN C4049644 Depression C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C2029884 Hearing loss by exam C0011168 Deglutition disorders HSDN C0015469 Facial paralysis C1864649 Myasthenia, limb-girdle, with tubular aggregates HPO C0030193 Sense of pain C0009946 Conversion disorder HSDN C0149651 Clubbing C0795878 Monosomy 22 MalaCards C2237041 Shox gene with short stature C3502054 Dentoleukoencephalopathy MalaCards C1962972 Proteinuria adverse event C0007222 Cardiovascular diseases HSDN C0018784 Deafness sensorineural C0016542 Foreign body HSDN C4084775 Usual severity weight loss C1366464 F9 gene HSDN C4085211 Pain distress question C0085129 Bronchial hyperreactivity HSDN C0036572 Convulsion C1963119 Stomach ulcer adverse event HSDN C2700617 Irritation - emotion C0342705 Folate malabsorption, hereditary MalaCards|HPO C2169806 Tic C2316212 Cryopyrin-associated periodic syndromes HSDN C0398650 Idiopathic thrombocytopenia purpura C0035229 Respiratory insufficiency HSDN C4084767 Bothered by vomiting C0007125 Carcinoma, ehrlich tumor HSDN C1963063 Anorexia adverse event C1552962 Units of measure - pica HSDN C3641756 Have diarrhea C0398691 Hyperimmunoglobulinemia d OrphaNet|HPO|MalaCards C0009676 Confusion state C0038395 Streptococcal infections HSDN C0009460 Communication impairment C0009244 Behavioral cognitive therapy HSDN C0036572 Convulsion C0035357 Retroperitoneal fibrosis HSDN C0007398 Catatonic C0019196 Hepatitis c HSDN C4085317 Diarrhea frequency C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C3146279 Coma C1855369 Maple syrup urine disease, type ia HPO C0039070 Collapse fleeting C0206586 Endolymphatic hydrops HSDN C4084727 Cough frequency C0027686 Pathologic neovascularization HSDN C0002170 Alopecia disorders C0795959 Gomez lopez hernandez syndrome OrphaNet|MalaCards C4084724 Usual severity constipation C0024299 Lymphoma HSDN C3898969 Have been vomiting C0042470 Guanarito haemorrhagic fever MalaCards C4084769 Vomiting frequency C0004161 Athletic injuries HSDN C0518090 Frequency of pain question C0038166 Staphylococcal skin infections HSDN C0026838 Spasticity muscle C0036421 Systemic scleroderma HSDN C0004134 Dyssynergia C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C1384666 Decreased hearing C1546949 Event consequence - death HSDN C2984058 Have pain C0036240 Response, satiety HSDN C4085317 Diarrhea frequency C0001144 Acne vulgaris HSDN C0030552 Paralysis partial C0752181 Central nervous system parasitic infections HSDN C0015970 Fever unknown origin C0860239 Catheter infections related HSDN C0000731 Abdomen distention C0021847 Intestinal pseudo-obstruction MalaCards C0015469 Facial paralysis C0006264 Bronchial neoplasms HSDN C0454542 Acquired stuttering C0038131 Stammer UMLS C2984057 Have nausea C1854107 Hyperaldosteronism, familial, type ii MalaCards C4084723 Constipation C0004275 Attitude health HSDN C0002170 Alopecia disorders C1535942 Autoimmune polyglandular syndrome type iii MalaCards C0035229 Respiratory function impaired C3278138 Fibrochondrogenesis 1 MalaCards C0018772 Deafness C0003486 Aortic aneurysm HSDN C3539020 Pelvic pain decreasing in frequency C0008519 Ectopic tissue HSDN C4054476 Monogenic obesity C0028754 Obesity UMLS C0030794 Pelvis pain C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0019825 Voice hoarseness C0012691 Dislocations HSDN C0026858 Musculoskeletal pain C0574960 Sacroiliitis HSDN C0030193 Sense of pain C0038002 Splenomegaly HSDN C0036572 Convulsion C1332865 Cavernous sinus meningioma UMLS C0004604 Pain back C0023418 Leukemia HSDN C0242936 Center pain C1962976 Ventricular fibrillation adverse event HSDN C0427055 Face weakness C1848030 Hypotonia-cystinuria syndrome MalaCards C4084897 Sleep disturbance subordinate domain C0751666 Canavan disease, infantile OrphaNet|HPO C4084768 Usual severity vomiting C0025222 Melena HSDN C0518090 Frequency of pain question C0033785 Pseudarthrosis HSDN C2984058 Have pain C0033054 Prenatal exposure delayed effects HSDN C1279888 Proteinuria of undiagnosed cause C0005659 Bite sting HSDN C0039870 Leanness C0019069 Hemophilia a HSDN C1856661 Cornea cloudy C0079588 Ichthyosis, x-linked OrphaNet|HPO|MalaCards C0242936 Center pain C0021125 Impulsive behavior HSDN C2984058 Have pain C0013537 Eclampsia HSDN C0000737 Abdomen pain C0278545 Stage iii rectal cancer ajcc v6 UMLS C0018681 Headache, cephalalgia C2673198 Familial cold autoinflammatory syndrome 2 MalaCards|HPO C3274924 Have been coughing C0012644 Animal disease models HSDN C0427055 Face weakness C0036202 Sarcoidosis MalaCards|HPO C1860844 Sparse, thin hair C1860823 Trichorhinophalangeal syndrome, type iii MalaCards|HPO C0040264 Ear ringing sound C0037313 Sleep HSDN C0020580 Decreased sensation C2242765 Acquired spondylolisthesis HSDN C0030486 Extremity paralysis, lower C1552262 Nurse practitioner - family HSDN C4084784 Diarrhea C0015927 Intrauterine fetal demise HSDN C1963281 Vomiting adverse event C0035435 Rheumatism HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014118 Endocarditis HSDN C0375570 Epigastric abdominal rigidity C0810319 Other and unspecified gastrointestinal disorders UMLS C0013362 Dysarthrias C1839028 Mitochondrial myopathy with diabetes MalaCards C3815497 Cough C0014859 Esophageal neoplasms OrphaNet|HSDN|MalaCards C0162298 Stiffness joints C3280054 Geleophysic dysplasia 2 MalaCards|UMLS C1557397 Adverse event associated with pain C0018924 Hemarthrosis HSDN C0184567 Pain acute C0021368 Inflammation HSDN C0018991 Paralysis one side of body C0006840 Candidiasis HSDN C0027796 Neuralgias C0018133 Graft-vs-host disease HSDN C0234132 Pyramidal sign C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards|UMLS C0002965 Crescendo angina C0009404 Colorectal neoplasms HSDN C0917816 Deficiency mental C0432242 Desbuquois syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C1867858 Prader-willi syndrome chromosome region HPO C0151786 Weakness muscle C0276226 Herpes encephalitis HSDN C4085210 Usual severity pain C0242658 Homosexuality male HSDN C0577567 Mass of urogenital structure C0269177 Polyp of broad ligament UMLS C0270948 Neurogenic muscular atrophy C0021368 Inflammation MalaCards C1557397 Adverse event associated with pain C2364172 Adherence to medication regime HSDN C3665347 Vision impaired C0687751 Acanthocytosis MalaCards C0042964 Anticipatory vomiting C0001546 Adjustment disorders HSDN C0497406 Over weight C0030297 Pancreatic neoplasm HSDN C0037199 Sinus infection C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive OrphaNet|MalaCards C4084723 Constipation C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0018784 Deafness sensorineural C1861481 Stickler syndrome, type 3 OrphaNet|HPO C0917816 Deficiency mental C3495588 Acrocephalopolydactylous dysplasia MalaCards C0231528 Muscle pain generalized C1861451 Stormorken syndrome MalaCards|UMLS C0028738 Nystagmus C2931356 Spastic paraplegia type 5a, recessive MalaCards C0848203 Male pelvic pain C3244301 Coverage level - family HSDN C0917816 Deficiency mental C3898580 Loeys-dietz syndrome type 2 MalaCards C0036572 Convulsion C0035126 Reperfusion injury HSDN C0029163 Hemorrhage mouth C0006436 Burning electric HSDN C0018772 Deafness C0751918 Cockayne pelizaeus merzbacher disease MalaCards C3541349 Syncope C0101725 Receptor for advanced glycation endproducts HSDN C0036572 Convulsion C0035334 Retinitis pigmentosa HSDN C0458090 Ureteric neuromuscular incoordination C0403608 Ureter UMLS C0036572 Convulsion C0035066 Renal artery obstruction HSDN C4084726 Distress cough C0011849 Diabetes mellitus HSDN C0429955 Bowels: occasional accident C0015732 Fecal incontinence UMLS C1963065 Apnea adverse event C0014850 Esophageal atresia HSDN C0015469 Facial paralysis C0026782 Mumps vaccine HSDN C3641755 Have constipation C0043251 Wounds and injuries HSDN C0003550 Broca aphasia C0004936 Mental disorders HSDN C1838869 Proximal neurogenic muscle weakness C0878677 Glycogen storage disease type iib MalaCards|HPO C3641756 Have diarrhea C0042133 Uterine fibroids HSDN C0242936 Center pain C0012746 Dissociative disorder HSDN C0009676 Confusion state C1532265 Encephalitis caused by siberian tick-borne encephalitis virus MalaCards C0518090 Frequency of pain question C0009081 Congenital clubfoot HSDN C0019825 Voice hoarseness C1334680 Mediastinal seminoma UMLS C0518090 Frequency of pain question C0040425 Tonsillitis HSDN C0917816 Deficiency mental C4012146 Desbuquois dysplasia 1 MalaCards C4085317 Diarrhea frequency C1857276 Trichohepatoenteric syndrome MalaCards|HPO C0700590 Diaphoresis excessive C1832409 Crisponi syndrome OrphaNet|HPO C0011991 Loose stools C0035091 Renal tubular transport, inborn errors HSDN C0151908 Dry skin C0265331 Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) MalaCards C0574002 Foot swelling C4015019 Neu-laxova syndrome 2 MalaCards|UMLS C0812426 Kidney problem C0747237 Papillary ductal stenosis UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0014550 Epilepsies, myoclonic HSDN C1549543 Administration method - pain C0026782 Mumps vaccine HSDN C1963091 Diarrhea adverse event C0020507 Hyperplasia HSDN C1963252 Tremor adverse event C0039082 Syndrome HSDN C1963252 Tremor adverse event C0027659 Neoplasms, experimental HSDN C0015230 Exanthem C1304060 Prurigo pattern atopic dermatitis UMLS C0014724 Burping C0276226 Herpes encephalitis HSDN C1557397 Adverse event associated with pain C4084971 Trachoma HSDN C0518090 Frequency of pain question C0034041 Puerperal infection HSDN C0031911 Pigment deposition C0456487 Peutz jeghers polyp MalaCards C1263846 Attention deficit disorder with hyperactivity C1844569 Faciogenital dysplasia with attention deficit-hyperactivity disorder HPO C0031911 Pigment deposition C1332356 Autonomic nervous system neoplasm MalaCards C0019079 Bloody sputum C0043255 Stab wound HSDN C0349506 Sun sensitivity C0432267 Tricho thiodystrophy disorder MalaCards|HPO C4084767 Bothered by vomiting C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3898969 Have been vomiting C0085096 Peripheral vascular diseases HSDN C4085661 Usual severity nausea C0019360 Herpes zoster disease HSDN C2919142 Short stature adverse event C1851879 Cleft lip with or without cleft palate, nonsyndromic, 8 HPO C0547030 Sensory perceptual alteration: visual C0348574 Visual disturbances in diseases classified elsewhere UMLS C0015469 Facial paralysis C1145670 Respiratory failure HSDN C2024878 Cardiovascular surgery result: dyspnea C1963229 Retinal detachment adverse event HSDN C0241137 Skin pallor C3541306 Plasmodium measurement HSDN C1962972 Proteinuria adverse event C0041956 Ureteral obstruction HSDN C0002962 Angina C0006261 Bronchial diseases HSDN C3539893 Pelvic pain occurs with intercourse C0021359 Infertility HSDN C0012833 Dizzy C0037369 Smoking HSDN C2984058 Have pain C2004493 Leukemia, b-cell HSDN C0013604 Edematous C0004442 Avoidance learning HSDN C0020672 Body temperature decreased C0033923 Psychomotor function HSDN C1963281 Vomiting adverse event C3814778 Hemolytic index HSDN C0015468 Face pain C0006434 Burn injury HSDN C0012569 Double vision C0008441 Chondroblastoma HSDN C0015672 Decreased energy C0031154 Peritonitis HSDN C0011168 Disorder deglutition C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C2024893 Cardiovascular surgery result: fatigue C0342442 Acth-dependent cushing's syndrome OrphaNet C0231712 Gait waddling C4015597 Myasthenic syndrome, congenital, 14 UMLS C4085548 Usual severity dizziness C0271355 Abducens nerve paralysis HSDN C0575081 Abnormal gait C0221060 Mobius syndrome MalaCards C0917816 Deficiency mental C0001193 Apert syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C0020627 Hypopharyngeal neoplasms HSDN C4085661 Usual severity nausea C0520679 Sleep apnea, obstructive HSDN C0018524 Hallucinate C0004442 Avoidance learning HSDN C1384666 Decreased hearing C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C1384666 Decreased hearing C0997768 Glaucoma HSDN C0151889 Reflexes tendon increased C0795949 Galloway mowat syndrome HPO C3815497 Cough C0023240 Legionellosis OrphaNet|MalaCards C1069915 Vertigo C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0019209 Large liver C1720861 Familial partial lipodystrophy, type 3 OrphaNet|HPO|MalaCards C3539896 Pelvic pain occurs with urination C0453996 Tobacco smoking HSDN C2911645 Weight loss adverse event C0473876 Cryptogenic tularaemia MalaCards C0349588 Stature short C2930900 Beta-sarcoglycanopathy MalaCards C0349506 Sun sensitivity C0162566 Porphyria cutanea tarda OrphaNet|MalaCards C0003862 Pain joint C0003838 Arterial occlusive diseases HSDN C4084727 Cough frequency C0016169 Pathologic fistula HSDN C1963071 Back pain adverse event C0206663 Neuroectodermal tumor, primitive MalaCards|HSDN C0033377 Caudal displacement C2748801 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement HPO C2203646 Jaundice C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0086437 Joint hypermobility C0220748 Cartilage-hair hypoplasia MalaCards|HPO C0000727 Abdomen acute C1962979 Burn adverse event HSDN C0000737 Abdomen pain C0040953 Trichotillomania HSDN C2911647 Weight gain adverse event C0036118 Salmonella infections, animal HSDN C0008031 Pain chest C0018813 Myocardial rupture HSDN C4084768 Usual severity vomiting C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C0030554 Abnormal sensation C1962963 Osteoporosis adverse event HSDN C0728710 Pupil constriction observed C0007350 Cat disease HSDN C0018784 Deafness sensorineural C1842124 Branchiootic syndrome 3 (disorder) HPO C1963087 Constipation adverse event C0027947 Neutropenia HSDN C0151908 Dry skin C0751434 Classical phenylketonuria MalaCards|HPO|UMLS C4085211 Pain distress question C0033117 Priapism HSDN C0700590 Diaphoresis excessive C1848947 Cold-induced sweating syndrome 1 HPO C4084767 Bothered by vomiting C0004052 Aspiration of vomitus HSDN C1963281 Vomiting adverse event C1864499 Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss HPO C2024893 Cardiovascular surgery result: fatigue C0019348 Herpes simplex infections HSDN C0004604 Pain back C0015726 Focused anxiety HSDN C1963154 Renal failure adverse event C1622345 Meretoja syndrome MalaCards C0009398 Color vision defects C0026850 Muscular dystrophy HSDN C1963071 Back pain adverse event C0016124 Finger injury HSDN C0018784 Deafness sensorineural C2239176 Liver carcinoma HSDN C1961131 Cough adverse event C2937358 Cerebral hemorrhage HSDN C0019572 Hairiness C2607929 Carney complex, type 1 OrphaNet|HPO|MalaCards C0031911 Pigment deposition C0349538 Anus; melanoma MalaCards C0010200 Cough symptom C0152018 Esophageal carcinoma OrphaNet|MalaCards C4085317 Diarrhea frequency C0018482 Haemophilus infections HSDN C0013528 Echo speech C0036602 Self stimulation HSDN C0162298 Stiffness joints C0018995 Hemochromatosis OrphaNet C0242936 Center pain C0024198 Lyme disease HSDN C1963065 Apnea adverse event C0036341 Schizophrenia HSDN C3641755 Have constipation C0007134 Renal cell carcinoma HSDN C0030193 Sense of pain C0162651 Gastric outlet obstruction HSDN C1557397 Adverse event associated with pain C0022353 Neonatal jaundice HSDN C2024893 Cardiovascular surgery result: fatigue C0020473 Hyperlipidemia HSDN C4085548 Usual severity dizziness C0032371 Poliomyelitis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome OrphaNet|MalaCards C3146279 Coma C0027643 Neoplasm recurrence, local HSDN C0575081 Abnormal gait C3536983 Familial hypophosphatemic rickets OrphaNet|HPO C1963077 Bone pain adverse event C0026764 Multiple myeloma OrphaNet|HPO C2203646 Jaundice C0027659 Neoplasms, experimental HSDN C1963091 Diarrhea adverse event C0019284 Diaphragmatic hernia HSDN C0700590 Diaphoresis excessive C1720189 Episodic ataxia MalaCards C0231218 Malaise generalized C1336456 Stage i hepatocellular carcinoma UMLS C4085210 Usual severity pain C0243013 Base learn problems HSDN C0027497 Queasy C1423541 Vangl2 gene HSDN C0005745 Blepharoptosis C1276035 Pena-shokeir syndrome type i MalaCards|HPO C3887638 Failure to thrive in infant C2931042 Hawkinsinuria OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C0007527 Cecal disease HSDN C4082202 Sleep quality question C0041466 Typhoid fever OrphaNet|MalaCards C4084774 Have weight loss C0018916 Hemangioma HSDN C1963091 Diarrhea adverse event C0009404 Colorectal neoplasms HSDN C0003910 Articulation disorder C0007760 Cerebellar diseases HSDN C0030486 Extremity paralysis, lower C0033975 Psychotic disorders HSDN C0020903 Illusion C4084909 Depression subordinate domain HSDN C0009421 Comatose C0020649 Hypotension HSDN C1279888 Proteinuria of undiagnosed cause C0162526 Aids-related opportunistic infections HSDN C0043094 Weight gain C0024115 Lung diseases HSDN C0000737 Abdomen pain C0235782 Gallbladder carcinoma OrphaNet C0013404 Respiratory difficulty C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0151889 Reflexes tendon increased C2931905 Olivopontocerebellar atrophy 3 MalaCards C1549543 Administration method - pain C0034494 Rabies (disorder) HSDN C0009421 Comatose C0497327 Dementia HSDN C0023014 Developmental disorder language C3813607 Infantile gastroesophageal reflux HSDN C0036572 Convulsion C0019322 Umbilical hernia HSDN C0025287 Meningitis-like C2015799 Other disease of neurological system UMLS C0015469 Facial paralysis C1456781 Benign melanocytic nevus HSDN C0018772 Deafness C0016065 Polyostotic fibrous dysplasia HPO C0231528 Muscle pain generalized C0010246 Coxsackievirus infections HSDN C0349588 Stature short C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C0241165 Skin thickening C2930971 Acroosteolysis dominant type MalaCards|HPO C0151786 Weakness muscle C0751549 Neurogenic thoracic outlet syndrome MalaCards C1000483 Genus anemia C0265265 Aase syndrome MalaCards C1535893 Orthostatic intolerance C0856761 Budd-chiari syndrome HSDN C0023015 Language handicap C0016952 Galactosemias HSDN C3539022 Pelvic pain decreasing in severity C0014179 Endometritis HSDN C0007758 Cerebellar ataxia C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0518090 Frequency of pain question C0702094 Agranulocytosis lab result HSDN C0040822 D tremors C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C4084774 Have weight loss C0004030 Aspergillosis HSDN C0030193 Sense of pain C0013592 Ectropion HSDN C1963093 Dizziness adverse event C3813607 Infantile gastroesophageal reflux HSDN C0018780 Frequencies hearing high loss C0022890 Labyrinthine disorder HSDN C4084773 Bothered by weight gain C0038354 Stomach diseases HSDN C0518090 Frequency of pain question C0027030 Maggot infection HSDN C0024312 Lymphocytopenia C1275050 Eosinophilia-myalgia syndrome from tryptophan OrphaNet|MalaCards C0030552 Paralysis partial C1865856 Neuropathy, hereditary thermosensitive MalaCards C0033774 Skin pruritus C0042826 Field visual HSDN C4084776 Weight loss C0085423 Gram-negative bacterial infections HSDN C0424755 Fever symptoms C3658261 Chemotherapy induced febrile neutropenia HSDN C4084897 Sleep disturbance subordinate domain C1970270 Choreoathetosis and congenital hypothyroidism HPO C2984058 Have pain C0221391 Melanosis coli HSDN C1963065 Apnea adverse event C0030305 Pancreatitis HSDN C0015672 Decreased energy C2827407 Infectious otitis media HSDN C0426579 Anorexia symptom C1962986 Glaucoma adverse event HSDN C4084766 Vomiting C0870082 Hyperkeratosis HSDN C1565249 Limitation, mobility C0597109 Nurse's role HSDN C0034124 Pupillary disorder C0153017 Encephalitis varicella HSDN C0917816 Deficiency mental C0268547 Argininosuccinic aciduria OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0037997 Splenic diseases HSDN C0917816 Deficiency mental C3809875 Van maldergem syndrome 2 MalaCards C0233844 Awkwardness C3151619 Ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation UMLS C4084784 Diarrhea C0029458 Osteoporosis, postmenopausal HSDN C0042963 Symptoms vomiting C0043065 Water electrolyte imbalance HSDN C0002962 Angina C0019326 Ventral hernia HSDN C0030193 Sense of pain C0393737 Episodic tension-type headache nos UMLS C0006370 Bulimia C0009240 Cognition HSDN C2025995 Cellulitis C0343101 Wells syndrome OrphaNet|MalaCards C1838869 Proximal neurogenic muscle weakness C1847759 Muscular dystrophy, congenital, 1c MalaCards|HPO C1962962 Hyperpigmentation adverse event C2677099 Crouzon syndrome with acanthosis nigricans (disorder) MalaCards C0349588 Stature short C1837884 Larsen-like syndrome MalaCards C0235153 Sensory hallucination C0023522 Leukodystrophy, metachromatic MalaCards|HPO C0013604 Edematous C0007453 Cattle disease HSDN C0349588 Stature short C1857276 Trichohepatoenteric syndrome MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0021655 Insulin resistance HSDN C0028738 Nystagmus C2676788 Joubert syndrome 9 (disorder) MalaCards|HPO C0151311 Cranial nerve palsy C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0151686 Growth retardation C2940786 Thyroid hormone resistance syndrome HPO C1856661 Cornea cloudy C3280231 Chromosome 8q21.11 deletion syndrome MalaCards C0020673 Hypothermia (central) (local) C0032851 Disease poultry HSDN C3539023 Pelvic pain increasing in frequency C0037072 Diseases sigmoid HSDN C4084776 Weight loss C0022423 Judgement HSDN C3539896 Pelvic pain occurs with urination C0026769 Multiple sclerosis HSDN C0270948 Neurogenic muscular atrophy C1837092 Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency HPO C1963170 Hypothermia adverse event C0010709 Cyst HSDN C0015300 Ocular proptosis C0271689 Insulin receptor, defect in HPO C0007758 Cerebellar ataxia C1851708 Encephalopathy, recurrent, of childhood MalaCards C4085222 Nausea C1955864 Cardiac sinus arrest HSDN C0349588 Stature short C0432233 Trichorhinophalangeal dysplasia type i MalaCards|HPO C2029884 Hearing loss by exam C0024636 Malocclusion HSDN C0344434 Atrial fibrillation ecg C1860752 Cardiomyopathy, familial hypertrophic, 7 HPO C0040822 D tremors C0036421 Systemic scleroderma HSDN C0013604 Edematous C0002736 Amyotrophic lateral sclerosis HSDN C2029884 Hearing loss by exam C1527231 Adrenomyeloneuropathy MalaCards C0271215 Blindness legal C1851402 Exudative vitreoretinopathy 1 MalaCards|HPO C0009806 Constipate C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant OrphaNet|HPO C2029884 Hearing loss by exam C0009244 Behavioral cognitive therapy HSDN C4084802 Usual severity diarrhea C2936917 Infantile polyarteritis MalaCards C2911645 Weight loss adverse event C0262627 Seroma HSDN C0851578 Disorder sleep C0017612 Glaucoma, open-angle HSDN C0024031 Back pain lower back C1552052 Religious affiliation - meditation HSDN C4084775 Usual severity weight loss C0039231 Tachycardia HSDN C3463815 Feel fatigue C0221074 Depression, postpartum HSDN C0007758 Cerebellar ataxia C1327916 Revesz syndrome (disorder) MalaCards|HPO C4084767 Bothered by vomiting C0001144 Acne vulgaris HSDN C4085210 Usual severity pain C0042514 Tachycardia, ventricular HSDN C0043144 Wheeze C0264414 Intrinsic asthma - no status UMLS C0413252 Hypothermia due to exposure C1963090 Dehydration adverse event HSDN C0151827 Pain eye C0035309 Retinal diseases HSDN C2911645 Weight loss adverse event C2239176 Liver carcinoma MalaCards C3815497 Cough C0027726 Nephrotic syndrome HSDN C1963093 Dizziness adverse event C0022665 Kidney neoplasm HSDN C4084784 Diarrhea C2931189 Neural crest tumor MalaCards C0026838 Spasticity muscle C0019699 Hiv seropositivity HSDN C0013144 Drowsy C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0013404 Respiratory difficulty C0812413 Malignant pleural mesothelioma UMLS C0392674 Exhausted C1861513 Cluster headache, familial UMLS C0043094 Weight gain C0011616 Contact dermatitis HSDN C0009763 Conjunctiva inflammation C0079474 Hallopeau-siemens disease HPO C0344428 Ventricular tachycardia by ecg finding C1969081 Arrhythmogenic right ventricular dysplasia, familial, 12 HPO C0036659 Sensation disorder C0032851 Disease poultry HSDN C0518090 Frequency of pain question C0158570 Vascular anomaly HSDN C0016382 Cutaneous vascular engorgement C0022661 Kidney failure, chronic HSDN C0848641 Lip rash C0007971 Cheilitis UMLS C0349588 Stature short C0265287 Acromicric dysplasia HPO C3641756 Have diarrhea C0030790 Pelvis infection HSDN C0003862 Pain joint C0156409 Atrophic vaginitis HSDN C2911645 Weight loss adverse event C0017181 Gastrointestinal hemorrhage HSDN C4084776 Weight loss C0205788 Histiocytoid hemangioma HSDN C2203646 Jaundice C2239176 Liver carcinoma MalaCards C0162298 Stiffness joints C0026272 Mixed connective tissue disease MalaCards C0022346 Yellow skin C0220847 C hepatitis virus HSDN C2242996 Tingling C0024473 Magnesium deficiency HSDN C0000737 Abdomen pain C0019360 Herpes zoster disease HSDN C0031911 Pigment deposition C0153416 Malig neop oth spec part oesop MalaCards C0006370 Bulimia C0032019 Pituitary neoplasms HSDN C0221166 Paraparesis C0334533 Arteriovenous hemangioma HSDN C4084768 Usual severity vomiting C1866495 Bartter syndrome, antenatal type 1 HPO C0243026 Generalized infection C1832241 Agammaglobulinemia due to early prob cell defect MalaCards|HPO C0009792 Consciousness disorder C1962958 Hematoma adverse event HSDN C0030552 Paralysis partial C0024198 Lyme disease MalaCards C1510456 Wernicke aphasia C0042830 Perception visual HSDN C4085211 Pain distress question C0036220 Kaposi sarcoma HSDN C0917816 Deficiency mental C1842534 Dystonia 18 (disorder) OrphaNet C0027498 Nausea vomiting C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C2203646 Jaundice C0017601 Glaucomas HSDN C0010520 Skin cyanosis C0004096 Asthma HSDN C4084768 Usual severity vomiting C0948089 Acute coronary syndrome HSDN C4025811 Anemic pallor C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C0522224 Palsied C0016537 Forearm injury HSDN C4084726 Distress cough C0007273 Carotid artery diseases HSDN C4084784 Diarrhea C1963266 Uveitis adverse event HSDN C0027796 Neuralgias C0477611 Spin osteochondrosis, unsp HSDN C4085317 Diarrhea frequency C0035637 Rinderpest HSDN C1962956 Flatulence adverse event C0034895 Rectovaginal fistula HSDN C0013421 Dystonia C0008625 Chromosome aberrations HSDN C3641756 Have diarrhea C0011311 Dengue fever MalaCards|HSDN C4084768 Usual severity vomiting C0031069 Familial mediterranean fever HSDN C1557397 Adverse event associated with pain C0040100 Thymoma HSDN C4084774 Have weight loss C1532560 Plasmacytoma - category HSDN C0008031 Pain chest C0016658 Fracture bone HSDN C1963091 Diarrhea adverse event C1367460 Lats1 gene HSDN C0030486 Extremity paralysis, lower C0004933 Behavior modification technique HSDN C4085317 Diarrhea frequency C0029877 Ear inflammation HSDN C3815497 Cough C0243025 Hantavirus pulmonary syndrome MalaCards C0030193 Sense of pain C0014901 Aesthetic HSDN C3641756 Have diarrhea C0034929 Reflex HSDN C0041667 Low weight C3554385 Congenital disorder of glycosylation, type iu MalaCards C2024878 Cardiovascular surgery result: dyspnea C0041466 Typhoid fever HSDN C0007758 Cerebellar ataxia C0270749 Marie cerebellar ataxia UMLS C0020672 Body temperature decreased C0035410 Rhabdomyolysis HSDN C3887638 Failure to thrive in infant C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C4085210 Usual severity pain C0041318 Tuberculosis, meningeal HSDN C0518090 Frequency of pain question C0040149 Subacute thyroiditis HSDN C3815497 Cough C0017178 Gastrointestinal diseases HSDN C0020673 Hypothermia (central) (local) C0016470 Food allergy HSDN C0007758 Cerebellar ataxia C3554607 Mitochondrial complex iii deficiency, nuclear type 4 MalaCards C1963086 Confusion adverse event C0085436 Meningitis, cryptococcal HSDN C0520966 Coordination impaired C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards|UMLS C1963252 Tremor adverse event C0019829 Hodgkin disease HSDN C2362324 Pediatric obesity C0027651 Tumor HSDN C0005745 Blepharoptosis C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0524910 Hepatitis c, chronic MalaCards C0026884 Muteness C0009241 Cognition disorders HSDN C0152169 Colic renal C0018099 Gout HSDN C0426579 Anorexia symptom C0023794 Lipoidosis HSDN C0013362 Dysarthrias C1865864 Amyotrophic lateral sclerosis 5 MalaCards|HPO C0270948 Neurogenic muscular atrophy C4015643 Combined oxidative phosphorylation deficiency 24 MalaCards C1959630 Eye pain adverse event C0015405 Fungal eye infections HSDN C0557874 Global developmental delay C3554226 Pch7 MalaCards C0018681 Headache, cephalalgia C0453996 Tobacco smoking HSDN C0011168 Disorder deglutition C0220756 Niemann-pick disease, type c OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0151526 Premature birth HSDN C0010520 Skin cyanosis C0018824 Heart valve disease HSDN C1549543 Administration method - pain C0024116 Lung diseases, fungal HSDN C0030193 Sense of pain C0018553 Hamartoma syndrome, multiple HSDN C0564823 Leg pain right C0810058 Other connective tissue disease UMLS C1961131 Cough adverse event C0007784 Cerebral hemisphere hemorrhage HSDN C2315100 Pediatric failure to thrive C3280296 Microcephaly-capillary malformation syndrome MalaCards C0086565 Liver function abnormal C1418533 Phka2 gene HPO C0030193 Sense of pain C0024959 Maxillary sinusitis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003467 Anxiety HSDN C0018681 Headache, cephalalgia C1142083 Embolia cutis medicamentosa HSDN C1963252 Tremor adverse event C0043251 Wounds and injuries HSDN C0424755 Fever symptoms C0021655 Insulin resistance HSDN C0241137 Skin pallor C0206603 Circoviridae infection HSDN C4085548 Usual severity dizziness C0004936 Mental disorders HSDN C0518090 Frequency of pain question C0001163 Vestibulocochlear nerve diseases HSDN C0020505 Excessive eating C0033973 Rational-emotive psychotherapy HSDN C0011168 Disorder deglutition C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) HPO C4084802 Usual severity diarrhea C0029463 Osteosarcoma HSDN C0850758 Pain pelvic C0004935 Animal ethology HSDN C2237041 Shox gene with short stature C2678045 Toe syndactyly, telecanthus, and anogenital and renal malformations OrphaNet|HPO C3898969 Have been vomiting C1456865 Ureteral calculi HSDN C4085211 Pain distress question C0029888 Otitis media purulent HSDN C0015676 Mental fatigue C2698559 Breakfast HSDN C0040034 Thrombocytopenia C0162530 Porphyria, erythropoietic HPO C0013604 Edematous C0035344 Retinopathy of prematurity HSDN C0557874 Global developmental delay C4014419 Xia-gibbs syndrome MalaCards C4084724 Usual severity constipation C0008628 Chromosome deletion HSDN C4084802 Usual severity diarrhea C2748662 Mitchell-riley syndrome MalaCards C4084766 Vomiting C0037274 Dermatologic disorders HSDN C1963086 Confusion adverse event C0025427 Mercury poisoning OrphaNet|MalaCards C0018834 Brash C1835664 Tylosis with esophageal cancer MalaCards C2024878 Cardiovascular surgery result: dyspnea C2717899 Upper extremity deep vein thrombosis HSDN C0003079 Pupillary inequality C0206368 Exfoliation syndrome MalaCards C4084768 Usual severity vomiting C0011603 Dermatitis HSDN C0020580 Decreased sensation C0003838 Arterial occlusive diseases HSDN C0027066 Myoclonic jerking C0027746 Nerve degeneration HSDN C0018681 Headache, cephalalgia C0280783 Juvenile pilocytic astrocytoma UMLS C0015469 Facial paralysis C0796274 Brown-vialetto-van laere syndrome OrphaNet|HPO|MalaCards C4084784 Diarrhea C0035435 Rheumatism HSDN C1557397 Adverse event associated with pain C0151740 Intracranial hypertension HSDN C0851578 Disorder sleep C0011603 Dermatitis HSDN C0011991 Loose stools C0031347 Pharyngeal neoplasms HSDN C0027498 Nausea vomiting C1868679 Griscelli syndrome, type 2 MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0013404 Respiratory difficulty C0013405 Dyspnea, paroxysmal UMLS C2984058 Have pain C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C0020580 Decreased sensation C0019348 Herpes simplex infections HSDN C0030193 Sense of pain C0280329 Glottic verrucous carcinoma UMLS C0043094 Weight gain C0034069 Pulmonary fibrosis HSDN C3815497 Cough C3809651 Infantile liver failure syndrome 2 MalaCards C0237326 Defecation pain C2717876 Aciduria, propionic OrphaNet|HPO C0042024 Urine incontinence C1556682 Adverse event associated with infection HSDN C1549543 Administration method - pain C0546952 Congenital facial asymmetry HSDN C0085636 Light sensitivity C1859439 Mopd iii UMLS C0234146 Absent reflex C1854154 Charcot-marie-tooth disease, type 2b1 HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0003125 Anorexia nervosa HSDN C0027796 Neuralgias C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0013604 Edematous C0016781 Fuchs endothelial dystrophy HSDN C4085211 Pain distress question C0032372 Poliomyelitis, anterior, acute HSDN C4049644 Depression C2936346 22q11 deletion syndrome MalaCards C1962972 Proteinuria adverse event C1860518 Vasculopathy, retinal, with cerebral leukodystrophy MalaCards|HPO C0002622 Amnesias C3850035 Decision making, intertemporal HSDN C0013604 Edematous C0029118 Opportunistic infections HSDN C0009806 Constipate C0036983 Septic shock HSDN C2911647 Weight gain adverse event C0002792 Anaphylaxis HSDN C1963281 Vomiting adverse event C0018567 Hand dermatoses HSDN C0033790 Pseudobulbar palsy C0276226 Herpes encephalitis HSDN C4084768 Usual severity vomiting C1420653 Tcn2 gene HPO C0010200 Cough symptom C0020541 Hypertension, portal HSDN C3814530 Skin vesicle C0867389 Chronic graft-versus-host disease MalaCards C0030193 Sense of pain C0014009 Empyema HSDN C0035229 Respiratory function impaired C0008728 Churg-strauss syndrome MalaCards C3539896 Pelvic pain occurs with urination C0027765 Nervous system disorder HSDN C0000737 Abdomen pain C1145628 Autonomic nervous system disorders HSDN C1962972 Proteinuria adverse event C0242231 Coronary stenosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0220981 Metabolic acidosis HSDN C1963065 Apnea adverse event C0000786 Spontaneous abortion HSDN C4085317 Diarrhea frequency C0008325 Cholecystitis HSDN C0424755 Fever symptoms C0018621 Hay fever HSDN C1963065 Apnea adverse event C1969084 Pontocerebellar hypoplasia type 6 MalaCards|HPO C3463815 Feel fatigue C0016563 Form perception HSDN C0018777 Deafness, conductive C1956097 Wolf-hirschhorn syndrome MalaCards|HPO C4085211 Pain distress question C0001163 Vestibulocochlear nerve diseases HSDN C0009676 Confusion state C0036349 Paranoid schizophrenia HSDN C0011991 Loose stools C0026636 Mouth diseases HSDN C0013362 Dysarthrias C3553948 Peroxisome biogenesis disorder 6b MalaCards C0030200 Intractable pain C0024299 Lymphoma HSDN C2911645 Weight loss adverse event C1299262 Sarcoma - category (morphologic abnormality) HSDN C0036572 Convulsion C0268193 Nadh cytochrome b5 reductase deficiency MalaCards|HPO|UMLS C0231712 Gait waddling C1865233 Muscular dystrophy, congenital, megaconial type MalaCards|HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0014848 Esophageal achalasia HSDN C0015672 Decreased energy C0079504 Hermanski-pudlak syndrome MalaCards C0027497 Queasy C0002989 Epithelioid hemangioma of skin HSDN C0018965 Blood urine C1832949 Infundibulopelvic dysgenesis MalaCards C0349489 Fetal hypoxia C0236969 Substance-related disorders HSDN C0398650 Idiopathic thrombocytopenia purpura C0037274 Dermatologic disorders HSDN C4084769 Vomiting frequency C1367460 Lats1 gene HSDN C0015672 Decreased energy C0027659 Neoplasms, experimental HSDN C0015970 Fever unknown origin C0031039 Effusion pericardial HSDN C4084763 Frequency of shortness of breath C0155877 Allergic asthma DiseaseOntology C0042963 Symptoms vomiting C3241945 Melena due to gastrointestinal hemorrhage HSDN C0030193 Sense of pain C0040381 Syndrome tolosa-hunt UMLS C2315100 Pediatric failure to thrive C1850597 Leigh syndrome due to mitochondrial complex ii deficiency HPO C2237041 Shox gene with short stature C0432227 Brachyolmia type 3 OrphaNet|HPO|MalaCards C3274924 Have been coughing C0013295 Duodenal ulcer HSDN C2984058 Have pain C0085605 Liver failure HSDN C0027497 Queasy C0600564 Self-efficacy HSDN C2911645 Weight loss adverse event C4050613 Anxiety scale (basc-2) HSDN C0042024 Urine incontinence C0036879 Education sex HSDN C0034151 Hyperglobulinemic purpura C0014457 Eosinophilia HSDN C4084723 Constipation C2931939 Idiopathic orthostatic hypotension MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0206663 Neuroectodermal tumor, primitive HSDN C0025323 Bleeding menstrual heavy C3150889 Factor v and factor viii, combined deficiency of, 2 HPO C0003862 Pain joint C0022665 Kidney neoplasm HSDN C0003811 Cardiac rhythm disturbance C2020284 Stickler syndrome, type 1 MalaCards C0040822 D tremors C1839576 Optic atrophy 2 (disorder) MalaCards C0015672 Decreased energy C0032343 Poisoning HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0042470 Guanarito haemorrhagic fever MalaCards C1963087 Constipation adverse event C3661523 Congenital intestinal aganglionosis OrphaNet|HPO|MalaCards C0086565 Liver function abnormal C1864668 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4 MalaCards|HPO C0237326 Defecation pain C0342859 Harderoporphyria HPO C0269268 Breast hardness C0332534 Induration UMLS C0000737 Abdomen pain C0009319 Colitis UMLS C0033774 Skin pruritus C0028796 Dermatitis, occupational UMLS C0241137 Skin pallor C0020532 Hypersplenism HSDN C2024878 Cardiovascular surgery result: dyspnea C0001231 Acth syndrome, ectopic HSDN C0040460 Dental pain C0043049 Water intoxication HSDN C0009806 Constipate C0032586 Polyradiculopathy HSDN C4085642 Level of joint stiffness C2931338 Chromosome 3, monosomy 3q13 OrphaNet|MalaCards C0237326 Defecation pain C1832370 Myopathy, myofibrillar, desmin-related MalaCards|HPO C1963071 Back pain adverse event C0003486 Aortic aneurysm HSDN C0030486 Extremity paralysis, lower C0020255 Hydrocephalus HSDN C2242996 Tingling C0717360 Disease lyme vaccine HSDN C4049644 Depression C0271097 Usher syndrome MalaCards C0522224 Palsied C0042830 Perception visual HSDN C2237041 Shox gene with short stature C3151211 Osteogenesis imperfecta, type x MalaCards|HPO C3641755 Have constipation C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C0014591 Bleeding nose C1956390 Cranial arteritis MalaCards C0012569 Double vision C0004106 Astigmatism HSDN C0037316 Not enough sleeping C1457883 Aggressive reaction HSDN C0006370 Bulimia C0525043 Attachment disorder reactive HSDN C0020673 Hypothermia (central) (local) C0018944 Hematoma HSDN C1963249 Tinnitus adverse event C0024121 Lung neoplasms HSDN C2984057 Have nausea C0019054 Hemolysis (disorder) HSDN C0221752 Rbc urine C0268250 Gaucher disease, type 2 (disorder) MalaCards C0018784 Deafness sensorineural C0011881 Diabetic nephropathy HSDN C0042798 Vision dim C0338503 Septo-optic dysplasia OrphaNet|HPO C0037316 Not enough sleeping C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C2032396 Pelvic pain on the right C0037397 Behavior social HSDN C2984058 Have pain C0007129 Merkel cell carcinoma MalaCards|HSDN C3541349 Syncope C1546654 Specimen source codes - granuloma HSDN C0020458 Hyperhydrosis C0001206 Acromegaly OrphaNet|HPO|MalaCards C0038002 Spleen enlargement C0035921 Congenital rubella syndrome OrphaNet|MalaCards C3463815 Feel fatigue C0206172 Diabetic foot HSDN C0005779 Clotting C3809522 Infantile liver failure syndrome 1 MalaCards C2024893 Cardiovascular surgery result: fatigue C2240378 Cleft palate on exam HSDN C1565249 Limitation, mobility C0242699 Bone demineralization, pathologic HSDN C0030193 Sense of pain C0025364 Mental status schedule HSDN C0398650 Idiopathic thrombocytopenia purpura C0027643 Neoplasm recurrence, local HSDN C0030975 Disorders perception C0205788 Histiocytoid hemangioma HSDN C0155344 Spasm of conjugated gaze C0497217 Other disease of eye UMLS C1963184 Nystagmus adverse event C0022336 Creutzfeldt-jakob disease MalaCards C4042891 Sleep wake disorders C2609414 Acute kidney injury HSDN C0020673 Hypothermia (central) (local) C0022758 Kap HSDN C0040259 Tinea pedis C3814530 Skin vesicle HSDN C2984057 Have nausea C0236969 Substance-related disorders HSDN C1963281 Vomiting adverse event C0029410 Osteoarthritis of hip HSDN C0162298 Stiffness joints C0039743 Thanatophoric dysplasia MalaCards C2032395 Pelvic pain on the left C0029436 Bone disease, disappearing HSDN C0242936 Center pain C0037397 Behavior social HSDN C0349588 Stature short C1859312 Camfak syndrome OrphaNet|HPO C2024878 Cardiovascular surgery result: dyspnea C0007350 Cat disease HSDN C0039231 Heartbeats increased C0085292 Stiff-person syndrome MalaCards C1557397 Adverse event associated with pain C0037073 Sigmoid neoplasms HSDN C4085222 Nausea C0679360 Foodborne disease HSDN C0023380 Lethargy C0268680 Biotin deficiency MalaCards C0037384 Snore C0040444 Migration, tooth HSDN C0427202 Atony, muscular C0152015 Bladder; inertia UMLS C0020672 Body temperature decreased C0007873 Uterine cervical neoplasm HSDN C0237326 Defecation pain C1864996 Enteric neuropathy, familial MalaCards C0031911 Pigment deposition C0751075 Cancer of digestive system MalaCards C0917816 Deficiency mental C0175695 Sotos' syndrome OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0268410 Acid phosphatase deficiency HPO C3463815 Feel fatigue C0036421 Systemic scleroderma OrphaNet|MalaCards C1963180 Neck pain adverse event C1546847 Entity name part type - family HSDN C1557397 Adverse event associated with pain C1547044 Kind of quantity - smell HSDN C0454644 Delayed language development C3150941 Rubinstein-taybi syndrome 2 MalaCards|HPO C0851578 Disorder sleep C0020544 Renal hypertension HSDN C0010200 Cough symptom C0007621 Neoplastic cell transformation HSDN C1963093 Dizziness adverse event C3495422 Finding relating to sexuality and sexual activity HSDN C0018784 Deafness sensorineural C1832390 Van maldergem wetzburger verloes syndrome MalaCards|HPO C0024031 Back pain lower back C0021843 Intestinal obstruction HSDN C0948992 Lower extremity paresthesia C0011860 Diabetes mellitus, non-insulin-dependent UMLS C4084802 Usual severity diarrhea C1420653 Tcn2 gene HPO C0018681 Headache, cephalalgia C0014347 Enterobacteriaceae infections HSDN C0020450 Hyperemesis gravidarum C0019285 Diaphragmatic hernia traumatic HSDN C0020673 Hypothermia (central) (local) C0027051 Myocardial infarction HSDN C0011206 Delirium acute C0019348 Herpes simplex infections HSDN C0036572 Convulsion C1504665 Products used to treat diabetic ketoacidosis HSDN C0262977 Decoloration skin C1704421 Skin pigmentation disorder UMLS C0242936 Center pain C0014061 Tick-borne encephalitis HSDN C2984058 Have pain C0042961 Intestinal volvulus HSDN C2315100 Pediatric failure to thrive C0151467 Addisonian crisis OrphaNet|MalaCards C0042024 Urine incontinence C0029928 Ovarian diseases HSDN C0011991 Loose stools C1843116 Bile acid synthesis defect, congenital, 1 MalaCards|HPO|UMLS C2362324 Pediatric obesity C0473527 Hypoalphalipoproteinemias HSDN C1557397 Adverse event associated with pain C2188545 Anuria HSDN C0270948 Neurogenic muscular atrophy C2677682 Rett syndrome, zappella variant HPO C0424755 Fever symptoms C0263662 Disseminated eosinophilic collagen disease HSDN C0019214 Hepatosplenomegaly C0745744 End stage liver disease UMLS C0020305 Fetal edema C0428953 Ecg infarction myocardial HSDN C0812426 Kidney problem C0748304 Renal failure chronic requiring dialysis UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0011603 Dermatitis HSDN C2957106 Headache severe C0021400 Influenza DiseaseOntology|MalaCards C1145670 Failure respiratory C0282577 Congenital disorders of glycosylation MalaCards C2024893 Cardiovascular surgery result: fatigue C0038441 Stress disorders, traumatic HSDN C2984058 Have pain C0010418 Cryptosporidiosis HSDN C3541349 Syncope C0012628 Discrete subaortic stenosis HSDN C3641756 Have diarrhea C0029877 Ear inflammation HSDN C0040264 Ear ringing sound C1552052 Religious affiliation - meditation HSDN C0042798 Vision dim C0042162 Uveal neoplasms HSDN C3815497 Cough C1527311 Brain edema HSDN C3887638 Failure to thrive in infant C1865639 Gracile bone dysplasia MalaCards|HPO C0006370 Bulimia C0028765 Behavior obsessive HSDN C0018524 Hallucinate C0162526 Aids-related opportunistic infections HSDN C0221232 Welts C0398776 Hereditary c1 esterase inhibitor deficiency - dysfunctional factor UMLS C0812426 Kidney problem C0078911 Aids-associated nephropathy UMLS C0085636 Light sensitivity C1415024 Opn1mw gene HPO C0020450 Hyperemesis gravidarum C1135956 Maternal fetal relations HSDN C0332563 Papulae C0014522 Epidermodysplasia verruciformis OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0997768 Glaucoma HSDN C0013390 Cramps menstrual C0041296 Tuberculosis HSDN C2984058 Have pain C0206693 Medullary carcinoma HSDN C1260880 Nasal drip C1333472 Adenocarcinoma of ethmoid sinus UMLS C3539890 Pelvic pain causes awakening at night C0040136 Thyroid neoplasm HSDN C0040034 Thrombocytopenia C1851970 Dyskeratosis congenita, autosomal dominant MalaCards|HPO C3274924 Have been coughing C0010823 Cytomegalovirus infections HSDN C0013604 Edematous C0409959 Osteoarthritis, knee HSDN C0221170 Stiffness muscle C1860157 Elejalde disease MalaCards C4085210 Usual severity pain C0032310 Pneumonia, viral HSDN C0015672 Decreased energy C1516552 Chronic idiopathic myelofibrosis, fibrotic stage UMLS C2127292 Fainting preceded by seeing blood C0340849 Fainting simple UMLS C3829611 Nausea frequency C0033893 Tension headache HSDN C0018834 Brash C3281084 Congenital disorder of glycosylation, type ir MalaCards C0007166 Cardiac output decreased C1963067 Atrial fibrillation adverse event HSDN C1443924 Severe diarrhea C1384687 Ancylostomiasis due to ancylostoma duodenale MalaCards C1962972 Proteinuria adverse event C0027765 Nervous system disorder HSDN C0427068 Legs weakness C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C0000737 Abdomen pain C1518749 Ovarian yolk sac tumor, polyvesicular vitelline pattern UMLS C0700590 Diaphoresis excessive C3714644 Thymus neoplasms MalaCards C0015672 Decreased energy C0040046 Thrombophlebitis HSDN C3829611 Nausea frequency C0024530 Malaria HSDN C0851578 Disorder sleep C0025303 Meningococcal infections HSDN C0042963 Symptoms vomiting C0017160 Gastroenteritis DiseaseOntology C0917816 Deficiency mental C0026654 Moyamoya disease OrphaNet|HPO C3641755 Have constipation C1000483 Genus anemia HSDN C4084802 Usual severity diarrhea C0276357 Swine influenza MalaCards C0034151 Hyperglobulinemic purpura C0038002 Splenomegaly HSDN C0004134 Dyssynergia C0023240 Legionellosis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0041972 Urethral obstruction HSDN C0011991 Loose stools C0032344 Poisoning aspects HSDN C0039870 Leanness C0010356 Cross infection HSDN C2029884 Hearing loss by exam C0005779 Blood coagulation disorders HSDN C1963281 Vomiting adverse event C0027819 Neuroblastoma HSDN C4084769 Vomiting frequency C0027661 Neoplasms, hormone-dependent HSDN C0027498 Nausea vomiting C1881600 Malignant vipoma MalaCards C4085210 Usual severity pain C0024796 Marfan syndrome HSDN C4085210 Usual severity pain C0001349 Acute-phase reaction HSDN C0033774 Skin pruritus C0009375 Colonic neoplasms HSDN C0033774 Skin pruritus C0010674 Cystic fibrosis HSDN C3146279 Coma C0024115 Lung diseases HSDN C0004604 Pain back C0019069 Hemophilia a HSDN C0426579 Anorexia symptom C1335686 Neuroendocrine neoplasm of rectum MalaCards C2911645 Weight loss adverse event C1322286 Thymoma, type c MalaCards C1963170 Hypothermia adverse event C0268353 Cutis laxa, x-linked MalaCards C1557397 Adverse event associated with pain C0034362 Q fever HSDN C1963281 Vomiting adverse event C0035222 Respiratory distress syndrome, adult HSDN C0018991 Paralysis one side of body C0041582 Ulcer HSDN C0004134 Dyssynergia C4014660 Combined oxidative phosphorylation deficiency 20 MalaCards C0013604 Edematous C0032827 Potassium deficiency HSDN C0009763 Conjunctiva inflammation C1858723 Poikiloderma with neutropenia MalaCards|HPO C1963063 Anorexia adverse event C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C2919142 Short stature adverse event C0796189 Prader-willi habitus-osteopenia-camptodactyly syndrome OrphaNet|MalaCards C1963249 Tinnitus adverse event C0029456 Osteoporosis HSDN C1557397 Adverse event associated with pain C0041316 Lymph node tuberculosis HSDN C0151205 Periorbital edema C4225184 Generalized lymphatic dysplasia of fotiou UMLS C1962972 Proteinuria adverse event C0344434 Atrial fibrillation ecg HSDN C0037771 Paraparesis spastic C0039841 Thiamine deficiency HSDN C0011991 Loose stools C0014866 Esophageal stenosis HSDN C3641755 Have constipation C0036864 Sexual relations HSDN C0700078 Deep tendon reflex decrease C0751918 Cockayne pelizaeus merzbacher disease MalaCards C3641755 Have constipation C0749420 Thyroid agenesis HPO C0848203 Male pelvic pain C0026857 Musculoskeletal diseases HSDN C3641755 Have constipation C0039614 Tetanus HSDN C0027497 Queasy C0276786 Human balantidiasis MalaCards C0086437 Joint hypermobility C0231586 Disorder, joint function UMLS C0557874 Global developmental delay C1857977 Microhydranencephaly MalaCards|HPO C0020505 Excessive eating C0010276 Craniopharyngioma MalaCards|HPO C0036572 Convulsion C2931542 Shapiro syndrome OrphaNet|MalaCards C0812426 Kidney problem C0748316 Renal insufficiency duration unknown UMLS C0027498 Nausea vomiting C0026691 Mucocutaneous lymph node syndrome MalaCards C3463815 Feel fatigue C1384514 Conn syndrome MalaCards C0231270 Fever factitious C0015480 Disorder factitious UMLS C4084767 Bothered by vomiting C0037933 Spinal diseases HSDN C0013911 Emaciate C0264766 Rheumatic mitral stenosis HSDN C0037316 Not enough sleeping C1548578 Location characteristic id - smoking HSDN C0008031 Pain chest C0153416 Malig neop oth spec part oesop MalaCards C1963091 Diarrhea adverse event C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0917816 Deficiency mental C0338503 Septo-optic dysplasia HPO C0012833 Dizzy C0019069 Hemophilia a HSDN C1963087 Constipation adverse event C0080179 Vertebra fracture HSDN C0007758 Cerebellar ataxia C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C4084802 Usual severity diarrhea C0264766 Rheumatic mitral stenosis HSDN C1549543 Administration method - pain C1254288 Anthrax HSDN C1557397 Adverse event associated with pain C0019522 Adenoma, sweat gland HSDN C1279888 Proteinuria of undiagnosed cause C0950123 Inborn genetic disease HSDN C0042571 Vertigo subjective C1963067 Atrial fibrillation adverse event HSDN C1279888 Proteinuria of undiagnosed cause C1384665 Hfe gene HSDN C3463815 Feel fatigue C0062527 Hepatitis b vaccine HSDN C0155552 Hearing loss mixed C2239112 Blister dosing unit HSDN C0085602 Polydypsia C0343068 Familial cold urticaria MalaCards|HPO C4085211 Pain distress question C0019569 Hirschsprung disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0021831 Intestinal diseases HSDN C0004604 Pain back C0021833 Intestinal fistula HSDN C0030193 Sense of pain C0030318 Panic state HSDN C0700072 Encounter due to stillbirth C0268412 Infantile hypophosphatasia HPO C0020672 Body temperature decreased C0016658 Fracture bone HSDN C4084768 Usual severity vomiting C1855371 Maple syrup urine disease, type ii HPO C0030193 Sense of pain C0029001 Onchocerciasis HSDN C2984058 Have pain C0030849 Penile neoplasms HSDN C1963086 Confusion adverse event C0342859 Harderoporphyria HPO C0812426 Kidney problem C0085548 Autosomal recessive polycystic kidney disease UMLS C0023012 Delay language C0473586 Michelin tire baby syndrome MalaCards|HPO C0042420 Vasovagal episode C0344315 Depressed mood HSDN C0017181 Gastrointestinal bleed C0024899 Mastocytosis MalaCards C4084773 Bothered by weight gain C0019693 Hiv infections HSDN C4042891 Sleep wake disorders C0282550 Persian gulf syndrome HSDN C0020639 Hypoproteinaemia C2931242 Familial waldmann's disease MalaCards C3463815 Feel fatigue C1556682 Adverse event associated with infection HSDN C1971624 Appetite absent C0033923 Psychomotor function HSDN C0015672 Decreased energy C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C3641895 Have dry mouth C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive MalaCards C0030193 Sense of pain C0001622 Adrenal gland hyperfunction HSDN C0558193 Extremity stiffness C1853100 Cerebrooculofacioskeletal syndrome 4 MalaCards|UMLS C0009460 Communication impairment C0016667 Fragile x syndrome HSDN C1384666 Decreased hearing C0262655 Recurrent urinary tract infection HSDN C0518090 Frequency of pain question C0596775 Behavior information seeking HSDN C3665492 Pigmentations C1334956 Neuroepithelial, perineurial, and schwann cell neoplasm MalaCards C0587246 Extremity weakness C1834336 Nemaline myopathy 3 HPO C0151686 Growth retardation C0431375 Classical lissencephaly MalaCards C0018681 Headache, cephalalgia C0751799 Brain hemorrhage, traumatic HSDN C0018681 Headache, cephalalgia C1333476 Ethmoid sinus schneiderian papilloma UMLS C0030193 Sense of pain C0085078 Lysosomal storage diseases HSDN C2096293 Ent surgical result ear vertigo C0453996 Tobacco smoking HSDN C0039070 Collapse fleeting C1970298 Progressive familial heart block, type ib MalaCards|HPO|UMLS C0518090 Frequency of pain question C0751955 Brain infarction HSDN C0000727 Abdomen acute C0033975 Psychotic disorders HSDN C0000737 Abdomen pain C0343208 Essential mixed cryoglobulinemia OrphaNet|MalaCards C0042024 Urine incontinence C0002949 Aneurysm, dissecting HSDN C3898969 Have been vomiting C0018273 Growth disorders HSDN C4084788 Have dizziness C1962963 Osteoporosis adverse event HSDN C0235153 Sensory hallucination C0268193 Nadh cytochrome b5 reductase deficiency HPO C0020673 Hypothermia (central) (local) C0022876 Premature obstetric labor HSDN C4084766 Vomiting C0035235 Respiratory syncytial virus infections HSDN C1963252 Tremor adverse event C0018790 Cardiac arrest HSDN C0413252 Hypothermia due to exposure C0011175 Dehydration HSDN C2203646 Jaundice C0149521 Pancreatitis, chronic MalaCards|HSDN C0005745 Blepharoptosis C3146244 Alcohol related birth defect OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0031111 Periostitis HSDN C4085642 Level of joint stiffness C1444838 Chronic arthritis of juvenile onset OrphaNet C0026821 Cramp C0011849 Diabetes mellitus HSDN C0857305 Thrombocytopenia purpura C0018915 Hemangioendothelioma HSDN C4084802 Usual severity diarrhea C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0004604 Pain back C0023801 Lipomatosis HSDN C1549543 Administration method - pain C0242891 Injuries teeth HSDN C2237041 Shox gene with short stature C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C0015402 Hemorrhage eye C0038940 Surgical wound dehiscence HSDN C0042963 Symptoms vomiting C0796561 Melanoma vaccines HSDN C0002962 Angina C0033817 Pseudomonas infections HSDN C0038506 Stutter C0010674 Cystic fibrosis HSDN C1384666 Decreased hearing C0149721 Left ventricular hypertrophy HSDN C4084774 Have weight loss C0031090 Periodontal diseases HSDN C0013456 Pain ear C0334299 Carcinoid tumor no icd-o subtype HSDN C0042571 Vertigo subjective C0027765 Nervous system disorder HSDN C0020672 Body temperature decreased C1261473 Sarcoma HSDN C4084774 Have weight loss C0038587 Substance withdrawal syndrome HSDN C0030554 Abnormal sensation C0221759 Brachial plexus neuritis OrphaNet|HPO|MalaCards C0151889 Reflexes tendon increased C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome OrphaNet|HPO|MalaCards C0003862 Pain joint C1956391 Temporal arteritis MalaCards|HPO C0003467 Angst C0162671 Melas syndrome OrphaNet|HPO|MalaCards C2984057 Have nausea C0275911 Tuberculosis of intestines MalaCards C3641756 Have diarrhea C0034040 Puerperal disorders HSDN C0024031 Back pain lower back C0020523 Immediate hypersensitivity HSDN C0040034 Thrombocytopenia C3554478 Osteopetrosis, autosomal recessive 8 MalaCards C0024031 Back pain lower back C1546847 Entity name part type - family HSDN C4085862 Bothered by nausea C0018800 Cardiomegaly HSDN C3898969 Have been vomiting C0011253 Delusions HSDN C0917816 Deficiency mental C1839736 Wilson-turner x-linked mental retardation syndrome HPO C1963093 Dizziness adverse event C0018213 Graves disease HSDN C3641755 Have constipation C1457883 Aggressive reaction HSDN C4084767 Bothered by vomiting C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C1963093 Dizziness adverse event C0018802 Congestive heart failure HSDN C4085210 Usual severity pain C0006430 Burning mouth syndrome HSDN C0003962 Ascites C0015656 Fasciolopsiasis DiseaseOntology C2024878 Cardiovascular surgery result: dyspnea C0035305 Retinal detachment HSDN C0036572 Convulsion C0010308 Congenital hypothyroidism HSDN C0030193 Sense of pain C0017154 Gastritis, atrophic HSDN C4084784 Diarrhea C0040046 Thrombophlebitis HSDN C4085210 Usual severity pain C0162700 Tick-borne diseases HSDN C2237041 Shox gene with short stature C2930866 Ramos arroyo clark syndrome MalaCards C0030486 Extremity paralysis, lower C0005891 Bodies image HSDN C0242936 Center pain C0237935 Trust HSDN C4084768 Usual severity vomiting C0039614 Tetanus HSDN C1961131 Cough adverse event C0700095 Central neuroblastoma HSDN C4042891 Sleep wake disorders C0596170 Binge eating disorder HSDN C0037316 Not enough sleeping C0005779 Blood coagulation disorders HSDN C1549543 Administration method - pain C0027126 Myotonic dystrophy HSDN C0036572 Convulsion C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0036572 Convulsion C0027873 Neuromyelitis optica MalaCards C1384666 Decreased hearing C0024534 Malaria, cerebral HSDN C3541349 Syncope C1836906 Arrhythmogenic right ventricular dysplasia, familial, 9 HPO C0234146 Absent reflex C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating MalaCards C4042891 Sleep wake disorders C0014549 Tonic-clonic epilepsy HSDN C0000737 Abdomen pain C0079293 Epidermolysis bullosa acquisita MalaCards C0010200 Cough symptom C0041318 Tuberculosis, meningeal HSDN C0009792 Consciousness disorder C0751741 Putamen hemorrhage HSDN C0973461 Dysphasia C0265249 Mietens' syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0016548 Foreign body migration HSDN C0424755 Fever symptoms C0019557 Hip fx HSDN C0004604 Pain back C0020615 Hypoglycemia HSDN C0010200 Cough symptom C0006277 Bronchitis MalaCards C4084723 Constipation C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C3274924 Have been coughing C0151744 Myocardial ischemia HSDN C0234132 Pyramidal sign C3809454 Hypotonia, infantile, with psychomotor retardation and characteristic facies 1 UMLS C0231528 Muscle pain generalized C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards|UMLS C2032395 Pelvic pain on the left C1546847 Entity name part type - family HSDN C0033377 Caudal displacement C0270972 Cornelia de lange syndrome OrphaNet|HPO|MalaCards C0038002 Spleen enlargement C0221013 Mastocytosis, systemic MalaCards C0007398 Catatonic C4042893 Person centered therapy HSDN C0030193 Sense of pain C0585474 Ewing's sarcoma of bone UMLS C3815497 Cough C0009187 Coccidiosis HSDN C0042963 Symptoms vomiting C0020621 Hypokalemia HSDN C0184567 Pain acute C1956346 Coronary artery disease HSDN C4084727 Cough frequency C0037361 Olfactory sense HSDN C0557874 Global developmental delay C3553449 Pontocerebellar hypoplasia, type 1b MalaCards C0000737 Abdomen pain C1882229 Ovarian thecoma MalaCards C0018681 Headache, cephalalgia C3665358 Galactorrhea HSDN C0036572 Convulsion C0039981 Thoracic neoplasms HSDN C1557397 Adverse event associated with pain C1175175 Severe acute respiratory syndrome HSDN C0349588 Stature short C0020557 Hypertriglyceridemia MalaCards C0013404 Respiratory difficulty C0026850 Muscular dystrophy HSDN C4084802 Usual severity diarrhea C0033626 Protein deficiency HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0021890 Intraoperative complications HSDN C0034150 Skin purpura C0007766 Intracranial aneurysm HSDN C3641756 Have diarrhea C0002989 Epithelioid hemangioma of skin HSDN C0812426 Kidney problem C0748199 Recurrent pyelonephritis UMLS C4085548 Usual severity dizziness C0271375 Cranial nerve palsy iv trochlear HSDN C1962957 Flushing adverse event C0079154 Congenital nonbullous ichthyosiform erythroderma HSDN C4084727 Cough frequency C0030305 Pancreatitis HSDN C3641756 Have diarrhea C0403447 Chronic kidney insufficiency HSDN C0271215 Blindness legal C0268342 Ehlers-danlos syndrome type 6 HPO C4085210 Usual severity pain C0037997 Splenic diseases HSDN C0242936 Center pain C0023891 Liver cirrhosis, alcoholic HSDN C0043094 Weight gain C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0027066 Myoclonic jerking C0002063 Alkalosis HSDN C0278152 Hemifacial spasms C0025284 Meningeal neoplasms MalaCards|HSDN C0497406 Over weight C0032584 Polyps HSDN C3887873 Hearing loss C3814778 Hemolytic index HSDN C1549543 Administration method - pain C0860239 Catheter infections related HSDN C0036572 Convulsion C0031350 Pharyngitis HSDN C1384666 Decreased hearing C0518449 Control of hip fracture risk HSDN C0557874 Global developmental delay C0265499 49,xxxxy chromosomal anomaly OrphaNet|MalaCards C0030193 Sense of pain C0036117 Salmonella infections HSDN C0518090 Frequency of pain question C0008732 Chylous ascites HSDN C4084802 Usual severity diarrhea C0007762 Cerebellar neoplasms HSDN C0221263 Cafe au lait spot C0238198 Gastrointestinal stromal tumors HSDN C1549543 Administration method - pain C0035229 Respiratory insufficiency HSDN C0003126 Smell loss C1563720 Kallmann syndrome 2 (disorder) MalaCards|HPO C3887873 Hearing loss C0022665 Kidney neoplasm HSDN C1962972 Proteinuria adverse event C0024115 Lung diseases HSDN C0151786 Weakness muscle C2963140 Arteriovenous fistula in use with two needles HSDN C0036572 Convulsion C0472352 Other specified generalized non-convulsive epilepsy UMLS C4084727 Cough frequency C0038661 Suicide HSDN C0460137 Push down or depress C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards C0009806 Constipate C0022650 Kidney calculi HSDN C4085210 Usual severity pain C0242966 Systemic inflammatory response syndrome HSDN C0015672 Decreased energy C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0234146 Absent reflex C3888087 Charcot-marie-tooth disease, type 2i MalaCards C0033774 Skin pruritus C3276706 Small fiber neuropathy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0038271 Stereotyped behavior HSDN C0917816 Deficiency mental C0003537 Aphasia MalaCards C0042963 Symptoms vomiting C0597109 Nurse's role HSDN C0020538 Hbp C1720860 Familial partial lipodystrophy, type 2 HPO C0013362 Dysarthrias C1868594 Perry syndrome MalaCards|HPO C0019209 Large liver C0158683 Polycystic liver disease OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C2936779 Hydroxymethylbilane synthase deficiency MalaCards C3665346 Loss sight C1956390 Cranial arteritis MalaCards C2237041 Shox gene with short stature C1837229 Muscular dystrophy, congenital, type 1d MalaCards|HPO C3665492 Pigmentations C0036631 Seminoma MalaCards C0018777 Deafness, conductive C0795825 Chromosome 8, trisomy 8p MalaCards C2984058 Have pain C0393571 Multiple system atrophy HSDN C0042963 Symptoms vomiting C0002514 Amino acid metabolism, inborn errors HSDN C4085642 Level of joint stiffness C1850865 Muscular dystrophy, congenital, producing arthrogryposis OrphaNet C0013394 Coitus painful C0006845 Candidiasis, chronic mucocutaneous OrphaNet|HPO|MalaCards C4082202 Sleep quality question C0752235 Lyme neuroborreliosis MalaCards C4084775 Usual severity weight loss C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C3463815 Feel fatigue C0007273 Carotid artery diseases HSDN C3665347 Vision impaired C0040560 Toxoplasmosis, congenital MalaCards C4085211 Pain distress question C1963088 Cystitis adverse event HSDN C4084776 Weight loss C0007453 Cattle disease HSDN C0349588 Stature short C2931232 Ventricular extrasystoles perodactyly robin sequence MalaCards C0575081 Abnormal gait C1845862 Creatine deficiency, x-linked MalaCards|HPO C3641756 Have diarrhea C0006057 Botulisms MalaCards C0018681 Headache, cephalalgia C2985220 Anaplastic medulloblastoma UMLS C0019079 Bloody sputum C0038358 Gastric ulcer HSDN C0004134 Dyssynergia C0019562 Von hippel-lindau syndrome OrphaNet|HPO|MalaCards C3539896 Pelvic pain occurs with urination C3244301 Coverage level - family HSDN C0013395 Indigestion C1333785 Gastric papillary adenocarcinoma UMLS C0041105 Jaw spasm C0031900 Pierre robin syndrome HSDN C0018777 Deafness, conductive C0007097 Carcinomas HSDN C0344315 Mood depressed C2931859 Acquired cjd MalaCards C0020455 Hypergammaglobulinemia C0011860 Diabetes mellitus, non-insulin-dependent HSDN C2203646 Jaundice C0005411 Biliary atresia MalaCards C1279888 Proteinuria of undiagnosed cause C1000483 Genus anemia HSDN C1549543 Administration method - pain C0027794 Neural tube defects HSDN C0004093 Asthenia C0282504 Environmental allergies HSDN C4085661 Usual severity nausea C0024115 Lung diseases HSDN C1962972 Proteinuria adverse event C0453996 Tobacco smoking HSDN C0004134 Dyssynergia C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C2237041 Shox gene with short stature C2675857 Holoprosencephaly 10 MalaCards C1557397 Adverse event associated with pain C0700345 Candidiasis, vulvovaginal HSDN C0151786 Weakness muscle C0268689 Vitamin d-dependent rickets, type 1 UMLS C4084776 Weight loss C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C3829611 Nausea frequency C0024198 Lyme disease HSDN C0413252 Hypothermia due to exposure C0024530 Malaria HSDN C0009792 Consciousness disorder C0275904 Tuberculosis, central nervous system HSDN C4084802 Usual severity diarrhea C0017601 Glaucomas HSDN C2024893 Cardiovascular surgery result: fatigue C0027126 Myotonic dystrophy HSDN C0151786 Weakness muscle C0003507 Aortic valve stenosis HSDN C0039870 Leanness C0600104 Obsessive compulsive behavior HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013124 Behavior drinking HSDN C3541349 Syncope C0003962 Ascites HSDN C0013404 Respiratory difficulty C0162770 Right ventricular hypertrophy HSDN C1963170 Hypothermia adverse event C1963215 Pneumothorax adverse event HSDN C3539020 Pelvic pain decreasing in frequency C0012746 Dissociative disorder HSDN C1963065 Apnea adverse event C1876185 Dysgnathia complex MalaCards C4084788 Have dizziness C0023470 Myeloid leukemia HSDN C0034155 Thrombotic thrombocytopenic purpura C0002063 Alkalosis HSDN C0026838 Spasticity muscle C0007453 Cattle disease HSDN C0751295 Memory loss or impairment C0038525 Subarachnoid hemorrhage UMLS C0000737 Abdomen pain C0009244 Behavioral cognitive therapy HSDN C3539891 Pelvic pain to the rear C0010068 Coronary heart disease HSDN C0162285 Edema eyelid C1843004 Hypotrichosis-lymphedema-telangiectasia syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0004364 Autoimmune diseases HSDN C0349588 Stature short C0271972 Thiamine-responsive megaloblastic anemia MalaCards C2919142 Short stature adverse event C1865639 Gracile bone dysplasia MalaCards|HPO C1961131 Cough adverse event C0339946 Pulmonary tularemia DiseaseOntology|MalaCards C4085222 Nausea C0003615 Appendicitis DiseaseOntology|HSDN|MalaCards C0424755 Fever symptoms C0267841 Acalculous cholecystitis HSDN C0151889 Reflexes tendon increased C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0349588 Stature short C3279716 Hypoacetylaspartia MalaCards C0010200 Cough symptom C0007453 Cattle disease HSDN C4084724 Usual severity constipation C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0919694 Ruminations nec C3272111 Merycism UMLS C0018681 Headache, cephalalgia C0018273 Growth disorders HSDN C1963091 Diarrhea adverse event C0043349 Xerophthalmia HSDN C1963063 Anorexia adverse event C0003864 Arthritis HSDN C2024893 Cardiovascular surgery result: fatigue C1522133 High cholesterol level HSDN C0020538 Hbp C0342750 Glycogen storage disease type id MalaCards|HPO C0522224 Palsied C0041601 Ulna fracture HSDN C0234146 Absent reflex C1837015 Ataxia, sensory, autosomal dominant MalaCards|HPO C0002963 Angina variant C0428977 Bradycardia HSDN C0018681 Headache, cephalalgia C0021400 Influenza HSDN C0008031 Pain chest C0152054 Therapeutic touch HSDN C0034124 Pupillary disorder C0038379 Eye deviation HSDN C3887638 Failure to thrive in infant C0265493 Cat eye syndrome MalaCards C0009806 Constipate C0007131 Non-small cell lung carcinoma HSDN C2024893 Cardiovascular surgery result: fatigue C0268450 Gitelman syndrome HSDN C2911647 Weight gain adverse event C0031345 Pharyngeal diseases HSDN C2919142 Short stature adverse event C1850343 Mosaic variegated aneuploidy syndrome OrphaNet|HPO|MalaCards C0002962 Angina C0872996 Q fever vaccine HSDN C0030486 Extremity paralysis, lower C0001883 Airway obstruction HSDN C4084802 Usual severity diarrhea C0268187 Alpha, alpha-trehalase deficiency MalaCards|HPO C1963281 Vomiting adverse event C0038159 Food poisoning, staphylococcal DiseaseOntology|MalaCards C2024893 Cardiovascular surgery result: fatigue C1862939 Amyotrophic lateral sclerosis 1 MalaCards C0030193 Sense of pain C0010692 Cystitis HSDN C4084773 Bothered by weight gain C1704272 Benign prostatic hyperplasia HSDN C0012833 Dizzy C3279664 Emberger syndrome MalaCards C0008031 Pain chest C0017500 Gestalt theories HSDN C0010200 Cough symptom C0007787 Transient ischemic attack HSDN C0042571 Vertigo subjective C0011854 Diabetes mellitus, insulin-dependent HSDN C1963252 Tremor adverse event C0034929 Reflex HSDN C4084802 Usual severity diarrhea C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0003862 Pain joint C1852456 Cryoglobulinemia, familial mixed OrphaNet|MalaCards C1145670 Failure respiratory C0265915 Congenital stenosis, pulmonary veins OrphaNet|MalaCards C0030552 Paralysis partial C3813553 Notch3 wt allele HSDN C4084768 Usual severity vomiting C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0030552 Paralysis partial C3279722 Myopathy, distal, 4 MalaCards C0150055 Pain chronic C0018674 Head trauma HSDN C0011206 Delirium acute C0206083 Myelinoclasis, central pontine HSDN C0018681 Headache, cephalalgia C0040809 Patient refusal of treatment HSDN C3539020 Pelvic pain decreasing in frequency C0033038 Ejaculatio praecox HSDN C0007859 Pain neck C0004153 Atherosclerosis HSDN C4084727 Cough frequency C0032298 Lipid pneumonia HSDN C0031256 Petechia C0376300 Dengue shock syndrome MalaCards C0000737 Abdomen pain C0279609 Blastema predominant wilms' tumor UMLS C0042420 Vasovagal episode C0439840 Reflex motion descriptor HSDN C4084775 Usual severity weight loss C0008533 Hemophilia b HSDN C0034150 Skin purpura C0030312 Pancytopenia HSDN C0012833 Dizzy C0338078 Non-functioning pituitary gland neoplasm MalaCards C0085593 Chill C0019103 Omsk haemorrhagic fever MalaCards C1963071 Back pain adverse event C3714509 Nutrition disorders HSDN C0019080 Bleed_nos problem C3160739 Fanconi anemia, complementation group e MalaCards C0018681 Headache, cephalalgia C0155862 Streptococcal pneumonia HSDN C0018524 Hallucinate C0029838 Other specified types of schizophrenia MalaCards C4084767 Bothered by vomiting C0032969 Pregnancy in diabetics HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004442 Avoidance learning HSDN C0454644 Delayed language development C2750234 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 MalaCards|HPO C1557397 Adverse event associated with pain C0028768 Obsessive-compulsive disorder HSDN C3665347 Vision impaired C0342770 Fumarase deficiency MalaCards|HPO C4084768 Usual severity vomiting C0034065 Pulmonary embolism HSDN C2029884 Hearing loss by exam C1861391 Symphalangism with multiple anomalies of hands and feet MalaCards C0015970 Fever unknown origin C0035357 Retroperitoneal fibrosis HSDN C4084724 Usual severity constipation C0043352 Xerostomia HSDN C0522224 Palsied C0031212 Personality disorders HSDN C4084784 Diarrhea C0002171 Alopecia areata HSDN C2984058 Have pain C3665624 Serum calcium below normal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162869 Aneurysm, ruptured HSDN C3146279 Coma C0002736 Amyotrophic lateral sclerosis HSDN C4085661 Usual severity nausea C0011616 Contact dermatitis HSDN C0026821 Cramp C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C0522224 Palsied C0850803 Anaphylaxis (non medication) HSDN C1549543 Administration method - pain C0334409 Leydig cell tumor, benign HSDN C0518090 Frequency of pain question C0014347 Enterobacteriaceae infections HSDN C0015732 Feces incontinence C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0221423 Ailment C0521839 Influenza-like illness UMLS C0700078 Deep tendon reflex decrease C0393547 Bulbospinal neuronopathy OrphaNet|HPO C1579931 Depressed - symptom C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C3815497 Cough C0021400 Influenza DiseaseOntology|MalaCards C0917816 Deficiency mental C2752047 Occipital atretic cephalocele, unusual facies, and large feet MalaCards C2024893 Cardiovascular surgery result: fatigue C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C4085211 Pain distress question C0039082 Syndrome HSDN C1145670 Failure respiratory C0795947 Fryns-van den berghe syndrome OrphaNet|MalaCards C1384666 Decreased hearing C1853490 22q13.3 deletion syndrome MalaCards|HPO C0003550 Broca aphasia C4049644 Depression HSDN C0151686 Growth retardation C1857495 Cardiocranial syndrome MalaCards C2315100 Pediatric failure to thrive C0265227 Schinzel-giedion syndrome HPO C2096293 Ent surgical result ear vertigo C0027765 Nervous system disorder HSDN C0020538 Hbp C0033845 Pseudotumor cerebri MalaCards C0034933 Abnormal reflexes C0036864 Sexual relations HSDN C1963077 Bone pain adverse event C1864997 Majeed syndrome OrphaNet|HPO|MalaCards C0085631 Abnormal excitement C3810814 Myocardial infarction ecg assessment HSDN C0011168 Disorder deglutition C2931395 Bulbospinal neuronopathy, x-linked recessive HPO C2984058 Have pain C0019337 Heroin dependence HSDN C0026826 High muscle tone C0238015 Autonomic dysreflexia HSDN C1963249 Tinnitus adverse event C0042568 Vertebrobasilar insufficiency HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085110 Severe combined immunodeficiency HSDN C0037315 Breathing disorder during sleeping C1846171 Lissencephaly, x-linked, 2 MalaCards C0003862 Pain joint C0033923 Psychomotor function HSDN C4084723 Constipation C1275808 Congenital central hypoventilation MalaCards|HPO C2911647 Weight gain adverse event C0023530 Leukopenia HSDN C0026838 Spasticity muscle C2931092 Maternally inherited leigh syndrome MalaCards C0000727 Abdomen acute C3163620 Hypotension adverse event HSDN C0009806 Constipate C0008625 Chromosome aberrations HSDN C0008031 Pain chest C1399352 Hemicrania, paroxysmal HSDN C0007758 Cerebellar ataxia C0016508 Congenital foot deformity HSDN C4084767 Bothered by vomiting C0162820 Dermatitis, allergic contact HSDN C2984058 Have pain C0027126 Myotonic dystrophy HSDN C0270948 Neurogenic muscular atrophy C0025239 Melorheostosis MalaCards C0000727 Abdomen acute C0850803 Anaphylaxis (non medication) HSDN C1963281 Vomiting adverse event C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C0013404 Respiratory difficulty C1145670 Respiratory failure UMLS C3463815 Feel fatigue C0017160 Gastroenteritis HSDN C0023012 Delay language C0265210 Weaver syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0001403 Addison disease OrphaNet C3641756 Have diarrhea C2937287 Hematolysis HSDN C2911645 Weight loss adverse event C0546323 Inferior vena cava membranous obstruction MalaCards C4085548 Usual severity dizziness C0011615 Dermatitis, atopic HSDN C0232493 Epigastric pain C0002871 Anemia UMLS C0700078 Deep tendon reflex decrease C3554129 Combined oxidative phosphorylation deficiency 13 MalaCards C4084802 Usual severity diarrhea C0236736 Cocaine-related disorders HSDN C4085661 Usual severity nausea C0042594 Vestibular diseases HSDN C0013404 Respiratory difficulty C1336184 Stage iib large cell carcinoma of lung UMLS C0018772 Deafness C0161409 Cochlear nerve damage HSDN C1963274 Vasculitis adverse event C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C0018784 Deafness sensorineural C1863561 Deafness, autosomal recessive 16 MalaCards|HPO C2032395 Pelvic pain on the left C0019066 Nontraumatic hemoperitoneum HSDN C0007758 Cerebellar ataxia C0497327 Dementia MalaCards C0011991 Loose stools C0035066 Renal artery obstruction HSDN C0000737 Abdomen pain C0003855 Arteriovenous fistula HSDN C0917816 Deficiency mental C2674127 Loeys dietz syndrome, type 2a (disorder) MalaCards C1962972 Proteinuria adverse event C0023968 Loiasis HSDN C0000737 Abdomen pain C0272295 Purpura, rheumatica MalaCards C3146279 Coma C0007795 Diffuse cerebral sclerosis of schilder HSDN C0030200 Intractable pain C0031118 Peripheral nervous system neoplasms HSDN C3274924 Have been coughing C2931854 Allergic bronchopulmonary mycosis MalaCards C0085602 Polydypsia C0153653 Malignant tumor of parathyroid gland MalaCards C1549543 Administration method - pain C0024636 Malocclusion HSDN C3665492 Pigmentations C0153459 Malignant neoplasm of body of pancreas MalaCards C2096293 Ent surgical result ear vertigo C0009240 Cognition HSDN C0036572 Convulsion C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO|UMLS C3641756 Have diarrhea C1704436 Peripheral arterial diseases HSDN C0004604 Pain back C0035956 Rupture spontaneous HSDN C0026858 Musculoskeletal pain C0029456 Osteoporosis HSDN C4084723 Constipation C0023890 Liver cirrhosis HSDN C0023012 Delay language C2363129 Benign rolandic epilepsy MalaCards C0026884 Muteness C0236642 Pick disease of the brain HSDN C3539020 Pelvic pain decreasing in frequency C0042029 Urinary tract infection HSDN C0041657 Consciousness loss C0017601 Glaucomas HSDN C0037316 Not enough sleeping C0221074 Depression, postpartum HSDN C4084769 Vomiting frequency C1546533 Specimen source codes - abscess HSDN C1279888 Proteinuria of undiagnosed cause C0013922 Embolism HSDN C4084788 Have dizziness C1546847 Entity name part type - family HSDN C0015672 Decreased energy C0034067 Pulmonary emphysema HSDN C0155047 Visual loss, both eyes unqual. C1263864 Blindness and/or vision impairment level UMLS C0034150 Skin purpura C0036864 Sexual relations HSDN C0018681 Headache, cephalalgia C0019569 Hirschsprung disease HSDN C0042963 Symptoms vomiting C0008775 Ciguatera poisoning HSDN C0522224 Palsied C0026598 Movement perception HSDN C0016382 Cutaneous vascular engorgement C4053907 Early onset tylosis MalaCards C2024893 Cardiovascular surgery result: fatigue C0595812 Fistula route HSDN C0018772 Deafness C0036875 Disorders of sex development HSDN C2919142 Short stature adverse event C0265291 Kenny-caffey syndrome MalaCards|HPO C0023012 Delay language C1412749 Bbs4 gene HPO C1961131 Cough adverse event C1762616 Meningioma, benign, no icd-o subtype HSDN C0042963 Symptoms vomiting C0003873 Rheumatoid arthritis HSDN C4084723 Constipation C0314657 Genetic predisposition HSDN C0013604 Edematous C0008066 Child behavior disorders HSDN C0349588 Stature short C1833699 Osteopoikilosis, isolated OrphaNet|HPO|MalaCards C0027498 Nausea vomiting C1866398 Proteus-like syndrome (disorder) MalaCards C0036572 Convulsion C3897752 Recurrent childhood glioblastoma UMLS C0042963 Symptoms vomiting C0405081 Mild hyperemesis-not delivered UMLS C4084788 Have dizziness C0037313 Sleep HSDN C0018784 Deafness sensorineural C0037315 Sleep apnea syndromes HSDN C4084784 Diarrhea C0037929 Spinal cord injuries HSDN C0231712 Gait waddling C0393946 Myasthenic myopathy MalaCards C0151786 Weakness muscle C0006109 Brain damage, chronic HSDN C3898969 Have been vomiting C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C0917816 Deficiency mental C0391826 Lhermitte-duclos disease MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0009763 Conjunctivitis HSDN C0013404 Respiratory difficulty C1546558 Specimen source codes - blister HSDN C0235267 Eye redness C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C0018681 Headache, cephalalgia C0458101 Cervicogenic headache UMLS C2911647 Weight gain adverse event C0007121 Bronchogenic carcinoma HSDN C1963249 Tinnitus adverse event C0025284 Meningeal neoplasms MalaCards|HSDN C0040460 Dental pain C0022362 Jaw diseases HSDN C0853945 Oral mucosa blister C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0016978 Gallbladder neoplasm HSDN C0018772 Deafness C1853490 22q13.3 deletion syndrome MalaCards|HPO C3641756 Have diarrhea C0206255 Malaria vaccine HSDN C0024031 Back pain lower back C0038539 Empyema, subdural HSDN C0497406 Over weight C0007873 Uterine cervical neoplasm HSDN C4085642 Level of joint stiffness C2931421 Brachytelephalangy characteristic facies kallmann OrphaNet|MalaCards C0557874 Global developmental delay C0268151 Classical galactosemia MalaCards C3829611 Nausea frequency C0007273 Carotid artery diseases HSDN C0018834 Brash C3280479 Pitt-hopkins-like syndrome 2 MalaCards C0151786 Weakness muscle C0023418 Leukemia HSDN C0009806 Constipate C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0241210 Speaking delay C3809872 Periventricular nodular heterotopia 6 MalaCards C0020673 Hypothermia (central) (local) C0038356 Stomach neoplasms HSDN C0030193 Sense of pain C0033845 Pseudotumor cerebri HSDN C0851578 Disorder sleep C0021125 Impulsive behavior HSDN C1963087 Constipation adverse event C0013502 Echinococcosis HSDN C0036572 Convulsion C2931646 Oculocerebral hypopigmentation syndrome type preus OrphaNet|MalaCards C0150055 Pain chronic C0042373 Vascular diseases HSDN C3829611 Nausea frequency C0007137 Squamous cell carcinoma HSDN C4084727 Cough frequency C0151744 Myocardial ischemia HSDN C1963091 Diarrhea adverse event C1801959 Histiocytic medullary reticulosis (disorder) MalaCards|HPO C4085211 Pain distress question C0025037 Meckel diverticulum HSDN C0003862 Pain joint C1304456 Congo hemorrhagic fever MalaCards C0041667 Low weight C1836861 Fanconi anemia, complementation group i MalaCards C0023530 Leukopenia C3151444 Dyskeratosis congenita, autosomal recessive, 4 MalaCards C1963177 Muscle pain adverse event C0268149 Glycogen storage disease type x MalaCards C4085317 Diarrhea frequency C0162820 Dermatitis, allergic contact HSDN C0042024 Urine incontinence C0037313 Sleep HSDN C0557874 Global developmental delay C4014742 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 MalaCards C0020505 Excessive eating C0025202 Melanoma HSDN C0151786 Weakness muscle C2939419 Cancer metastatic UMLS C0015938 Fetal macrosomia C0007222 Cardiovascular diseases HSDN C0011991 Loose stools C0398623 Thrombophilia HSDN C0518090 Frequency of pain question C0002453 Amenorrhea HSDN C0233794 Memory impaired C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0009398 Color vision defects C0039336 Gustatory sense HSDN C4084802 Usual severity diarrhea C0037356 Smallpox virus HSDN C0151786 Weakness muscle C0007965 Chediak-higashi syndrome MalaCards|UMLS C0751495 Seizure focal C1858673 Generalized epilepsy with febrile seizures plus, type 2 UMLS C0042940 Disorder of voice C0001175 Acquired immunodeficiency syndrome HSDN C0032617 High urine output C1302808 Myopericytoma HSDN C0020305 Fetal edema C1963162 Lymphocele adverse event HSDN C0010200 Cough symptom C0017612 Glaucoma, open-angle HSDN C0020455 Hypergammaglobulinemia C0086438 Hypogammaglobulinemia MalaCards C2237041 Shox gene with short stature C1834880 Dominantly inherited bone dysplasia with severe eye involvement MalaCards C4084773 Bothered by weight gain C0006434 Burn injury HSDN C4084788 Have dizziness C0752322 Epilepsy, partial, sensory HSDN C0413252 Hypothermia due to exposure C0034067 Pulmonary emphysema HSDN C0151786 Weakness muscle C0086922 Purpura rheumatoid MalaCards C1963071 Back pain adverse event C0017563 Gingival diseases HSDN C0011168 Disorder deglutition C0238190 Inclusion body myositis (disorder) MalaCards C0022568 Inflammation corneal C0265201 De sanctis-cacchione syndrome MalaCards|HPO C0007398 Catatonic C0001726 Affective symptoms HSDN C0277959 Hair coarseness C0344487 Lateral meningocele MalaCards C4085211 Pain distress question C0037397 Behavior social HSDN C0030552 Paralysis partial C0037579 Soft tissue neoplasms HSDN C0151786 Weakness muscle C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0020580 Decreased sensation C0024958 Maxillary sinus neoplasms HSDN C0240715 Perineal lump C0346791 Melanoma; perineum UMLS C4084776 Weight loss C0026948 Mycosis fungoides HSDN C0009806 Constipate C1836522 Schindler disease, type ii MalaCards C0002622 Amnesias C0009426 Combat disorders HSDN C0005745 Blepharoptosis C1837819 Cerebrofrontofacial syndrome MalaCards C1962957 Flushing adverse event C0001231 Acth syndrome, ectopic HSDN C0221170 Stiffness muscle C0406612 Encephalocraniocutaneous lipomatosis OrphaNet|MalaCards C2237041 Shox gene with short stature C1844853 Brachytelephalangic chondrodysplasia punctata HPO C4085862 Bothered by nausea C0027809 Neurilemmoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018467 Habituation, psychophysiologic HSDN C2096293 Ent surgical result ear vertigo C0018800 Cardiomegaly HSDN C2126985 Binocular epiphora C0152227 Excessive tearing UMLS C4084725 Usual severity cough C0085167 Granular cell tumor HSDN C0542476 Forgetful C1843015 Alzheimer disease, familial, 3, with spastic paraparesis and apraxia HPO C1549543 Administration method - pain C0018816 Heart septal defects HSDN C0020538 Hbp C0001206 Acromegaly OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0040948 Trichostrongyliasis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0005586 Bipolar disorder HSDN C0851578 Disorder sleep C0002871 Anemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027721 Lipoid nephrosis HSDN C1557397 Adverse event associated with pain C0032708 Disorders of porphyrin metabolism HSDN C0018772 Deafness C0001584 Adolescent psychology HSDN C0030200 Intractable pain C0017168 Gastroesophageal reflux disease HSDN C0004134 Dyssynergia C0085096 Peripheral vascular diseases HSDN C0002962 Angina C0002986 Fabry disease MalaCards|HPO C0743317 Dysphagia chronic C0011168 Deglutition disorders UMLS C3178766 Nociceptive pain C0600467 Neurogenic inflammation HSDN C4085862 Bothered by nausea C0043065 Water electrolyte imbalance HSDN C2919142 Short stature adverse event C0271695 Rabson-mendenhall syndrome OrphaNet|HPO C0751495 Seizure focal C1263858 Muscular dystrophy congenital, merosin negative HPO C3641755 Have constipation C0008924 Cleft lip HSDN C0002963 Angina variant C0008728 Churg-strauss syndrome HSDN C4084768 Usual severity vomiting C0700327 Clinical findings relating to memory HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0022658 Kidney diseases HSDN C3887638 Failure to thrive in infant C0242621 Isochromosomes HSDN C4085222 Nausea C1299624 Postural orthostatic tachycardia syndrome HSDN C0026838 Spasticity muscle C0020179 Huntington disease OrphaNet|HPO|MalaCards C1384666 Decreased hearing C0035923 German measles vaccine HSDN C0026858 Musculoskeletal pain C0205906 Sex bias HSDN C0018777 Deafness, conductive C0020534 Orbital separation excessive HSDN C4085317 Diarrhea frequency C0037072 Diseases sigmoid HSDN C1971624 Appetite absent C1535917 Nipah virus infection MalaCards C1549543 Administration method - pain C1862939 Amyotrophic lateral sclerosis 1 MalaCards C0013404 Respiratory difficulty C3501858 Muscular dystrophy, limb-girdle, type 1d MalaCards C0012833 Dizzy C0029883 Otitis media with effusion HSDN C2984058 Have pain C0021345 Infectious mononucleosis HSDN C0270948 Neurogenic muscular atrophy C1837094 Myasthenic syndrome, congenital, ie MalaCards|HPO C3641755 Have constipation C0033975 Psychotic disorders HSDN C0011991 Loose stools C0027819 Neuroblastoma MalaCards|HSDN C0013604 Edematous C0027627 Neoplasm metastasis HSDN C0150045 Urinary incontinence urge C0085392 Bacteroidaceae infection HSDN C1963063 Anorexia adverse event C0038941 Incisional infection HSDN C0036572 Convulsion C1541316 Adult giant cell glioblastoma UMLS C4042891 Sleep wake disorders C0011603 Dermatitis HSDN C0030193 Sense of pain C1333473 Adenoid cystic carcinoma of ethmoid sinus UMLS C1963064 Anxiety adverse event C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C0036572 Convulsion C0037006 Shoulder fracture HSDN C1384666 Decreased hearing C0001584 Adolescent psychology HSDN C0037317 Sleep disturbance C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO|UMLS C0917816 Deficiency mental C0015938 Fetal macrosomia MalaCards C1557397 Adverse event associated with pain C0021568 Bites insect stings HSDN C2024893 Cardiovascular surgery result: fatigue C0032269 Pneumococcal infections HSDN C0013604 Edematous C0016053 Fibromyalgia HSDN C0038002 Spleen enlargement C0036221 Mast-cell sarcoma OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C0015695 Fatty liver HSDN C2984057 Have nausea C0037274 Dermatologic disorders HSDN C0013421 Dystonia C0035372 Rett syndrome OrphaNet|HSDN|HPO|MalaCards C1962956 Flatulence adverse event C0007453 Cattle disease HSDN C0042963 Symptoms vomiting C0037926 Compression of spinal cord HSDN C0557874 Global developmental delay C1837819 Cerebrofrontofacial syndrome MalaCards C4084727 Cough frequency C0001430 Adenoma HSDN C1145670 Failure respiratory C0342720 Adenosylcobalamin synthesis defect MalaCards C4085211 Pain distress question C0751931 Femoral lesion nerve HSDN C2984058 Have pain C0030271 Pancoast syndrome HSDN C0032617 High urine output C0810038 Genitourinary symptoms and ill-defined conditions UMLS C2032395 Pelvic pain on the left C0009373 Colonic diseases HSDN C3898969 Have been vomiting C0019310 Hernia, obturator HSDN C0036572 Convulsion C3149750 Mitochondrial dna depletion syndrome 2 (myopathic type) MalaCards|HPO C0518090 Frequency of pain question C0600040 Chronic interstitial cystitis OrphaNet C0542476 Forgetful C2702698 Forgetting names UMLS C0042798 Vision dim C0035320 Retinal neovascularization HSDN C0518090 Frequency of pain question C0013502 Echinococcosis HSDN C0030554 Abnormal sensation C1836544 Schindler disease, type i MalaCards|HPO C3887873 Hearing loss C0026946 Mycoses HSDN C3463815 Feel fatigue C1866552 Paragangliomas 2 (disorder) MalaCards C0036572 Convulsion C3502492 Microcephaly with chorioretinopathy, autosomal recessive OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0011849 Diabetes mellitus HSDN C0426579 Anorexia symptom C1556682 Adverse event associated with infection HSDN C0015230 Exanthem C1827808 Viral exanthem due to chicken pox UMLS C0018524 Hallucinate C0001418 Adenocarcinoma HSDN C0424755 Fever symptoms C0345904 Malignant neoplasm of liver MalaCards C2911647 Weight gain adverse event C0026848 Myopathy HSDN C3665346 Loss sight C0809996 Blindness and vision defects UMLS C2203646 Jaundice C0023904 Liver neoplasms, experimental HSDN C1963252 Tremor adverse event C0344423 Atrial flutter by ecg finding HSDN C4084802 Usual severity diarrhea C2931402 Lubani al saleh teebi syndrome OrphaNet|MalaCards C0040485 Wryneck C0037051 Behavior illness HSDN C0007384 Cataplexy C1850363 Niemann-pick disease, nova scotian type HPO C4085222 Nausea C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C3815497 Cough C0007138 Carcinoma, transitional cell HSDN C1963281 Vomiting adverse event C0023283 Leishmaniasis, cutaneous HSDN C4084726 Distress cough C0027439 Nasopharyngeal neoplasms HSDN C4085211 Pain distress question C0029124 Optic atrophy HSDN C4084769 Vomiting frequency C0042830 Perception visual HSDN C4084802 Usual severity diarrhea C0017416 Genital neoplasms, female HSDN C0042963 Symptoms vomiting C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C0518090 Frequency of pain question C0028432 Nose diseases HSDN C1963065 Apnea adverse event C0036323 Schistosomiasis HSDN C0030193 Sense of pain C0037221 Situs inversus HSDN C3898969 Have been vomiting C0041952 Uerterolithiasis HSDN C4085549 Dizziness C0001580 Adolescent behavior HSDN C3541349 Syncope C1704972 Genomic orientation HSDN C0021368 Inflammation C1850406 Navajo neurohepatopathy MalaCards C0577567 Mass of urogenital structure C0037859 Spermatocele UMLS C1963093 Dizziness adverse event C0600260 Lung diseases, obstructive HSDN C2911647 Weight gain adverse event C0600518 Choroidal neovascularization HSDN C0013362 Dysarthrias C0011849 Diabetes mellitus HSDN C4050613 Anxiety C0206667 Adrenal cortical adenoma MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4085211 Pain distress question C0023787 Lipodystrophy HSDN C2984058 Have pain C0022904 Lacrimal apparatus diseases HSDN C4085210 Usual severity pain C3896673 Familial nonmedullary thyroid gland carcinoma MalaCards C1963087 Constipation adverse event C0003493 Aortic diseases HSDN C0018784 Deafness sensorineural C0751878 Vasculitis, central nervous system HSDN C0012833 Dizzy C0677866 Brain stem neoplasms HSDN C0015469 Facial paralysis C0018790 Cardiac arrest HSDN C0011206 Delirium acute C0340629 Aortic aneurysm without mention of rupture nos HSDN C0007758 Cerebellar ataxia C0011265 Presenile dementia MalaCards C4085222 Nausea C0162651 Gastric outlet obstruction HSDN C4085862 Bothered by nausea C0700095 Central neuroblastoma HSDN C4084769 Vomiting frequency C0033586 Failure, prosthesis HSDN C0030200 Intractable pain C0007222 Cardiovascular diseases HSDN C3898969 Have been vomiting C0431109 Choroid plexus carcinoma HPO C4084769 Vomiting frequency C0268547 Argininosuccinic aciduria MalaCards|HPO C0233565 Bradykinesia C3809811 Parkinson disease 19, juvenile-onset UMLS C0522224 Palsied C0018794 Heart block HSDN C4084802 Usual severity diarrhea C0037930 Spinal cord neoplasms HSDN C0000737 Abdomen pain C0750426 Wbc elevated HSDN C0023015 Language handicap C3146297 Study of behavior during childhood HSDN C0015672 Decreased energy C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C1000483 Genus anemia C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C4084788 Have dizziness C0009450 Disease caused by microorganism HSDN C0022346 Yellow skin C0016154 Fish disease HSDN C4084723 Constipation C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards C4084775 Usual severity weight loss C2698559 Breakfast HSDN C4084802 Usual severity diarrhea C0017205 Gaucher disease HSDN C1971624 Appetite absent C0035243 Respiratory tract infections HSDN C2237041 Shox gene with short stature C1859965 Alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus MalaCards C3887638 Failure to thrive in infant C0795917 Alpha-thalassemia mental retardation syndrome, deletion-type OrphaNet|HPO|MalaCards C3539895 Pelvic pain occurs with bowel movement C2984291 Glioblastoma multiforme pathway HSDN C0031911 Pigment deposition C0684743 Malignant neoplasm of muscle MalaCards C0027066 Myoclonic jerking C3539916 Myoclonus, familial cortical MalaCards C3641755 Have constipation C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C1720777 Functional laterality HSDN C4084775 Usual severity weight loss C0854795 Resectable hepatic malignant neoplasm MalaCards C1963091 Diarrhea adverse event C0850803 Anaphylaxis (non medication) HSDN C0020458 Hyperhydrosis C4053907 Early onset tylosis MalaCards C2911647 Weight gain adverse event C0019337 Heroin dependence HSDN C0015970 Fever unknown origin C0018482 Haemophilus infections HSDN C0234146 Absent reflex C0011195 Dejerine-sottas disease (disorder) HPO C4084725 Usual severity cough C0149514 Bronchitis acute MalaCards C4085549 Dizziness C1579931 Depressed - symptom HSDN C4085211 Pain distress question C0010246 Coxsackievirus infections HSDN C0028738 Nystagmus C1861829 Cataract microcornea syndrome MalaCards|HPO C0015300 Ocular proptosis C2020284 Stickler syndrome, type 1 OrphaNet|HPO|MalaCards C0027066 Myoclonic jerking C0030568 Parkinsonism, postencephalitic HSDN C0012833 Dizzy C0033873 Psychiatry HSDN C2911647 Weight gain adverse event C0027902 Neuropsychological diagnosis HSDN C0398650 Idiopathic thrombocytopenia purpura C0042487 Venous thrombosis HSDN C0750426 Wbc elevated C0085253 Adult-onset still disease OrphaNet|MalaCards C0242936 Center pain C3827868 Tachycardia by ecg finding HSDN C0020578 Hyperventilate C0035400 Reyes syndrome HSDN C4084766 Vomiting C0342859 Harderoporphyria HPO C0042024 Urine incontinence C1963106 Esophagitis adverse event HSDN C0451941 Itch scrotum C0459151 Disorder of soft tissue of trunk UMLS C0040460 Dental pain C0236969 Substance-related disorders HSDN C0007814 Cerebrospinal fluid otorrhea C0039144 Syringomyelia HSDN C0003862 Pain joint C1837218 Cleft palate, isolated HSDN C0030554 Abnormal sensation C0003838 Arterial occlusive diseases HSDN C3641756 Have diarrhea C2931402 Lubani al saleh teebi syndrome OrphaNet|MalaCards C3274924 Have been coughing C0021799 Interprofessional relations HSDN C2984057 Have nausea C0022758 Kap HSDN C0030193 Sense of pain C0043324 Juvenile xanthogranuloma HSDN C4084727 Cough frequency C1963084 Colitis adverse event HSDN C0036572 Convulsion C1553188 Hemolysis - observation HSDN C0040460 Dental pain C0010054 Coronary arteriosclerosis HSDN C1963180 Neck pain adverse event C0016548 Foreign body migration HSDN C4085549 Dizziness C0017601 Glaucomas HSDN C0027066 Myoclonic jerking C1850055 Peho syndrome MalaCards C0037763 Spasm C0020443 Hypercholesterolemia HSDN C1962972 Proteinuria adverse event C0032584 Polyps HSDN C0013404 Respiratory difficulty C0014860 Perforation esophagus HSDN C4085211 Pain distress question C0236792 Asperger syndrome HSDN C0000737 Abdomen pain C0005690 Bladder fistula HSDN C1279888 Proteinuria of undiagnosed cause C0027412 Opioid-related disorders HSDN C0242936 Center pain C0162869 Aneurysm, ruptured HSDN C4084725 Usual severity cough C0030297 Pancreatic neoplasm HSDN C0018784 Deafness sensorineural C0019569 Hirschsprung disease MalaCards|HPO C3887873 Hearing loss C0007453 Cattle disease HSDN C0232466 Feeding difficulty C0751885 Myasthenic syndromes, congenital, slow channel MalaCards|HPO C0518090 Frequency of pain question C0002351 Altitude sickness HSDN C0010520 Skin cyanosis C0024299 Lymphoma HSDN C1962962 Hyperpigmentation adverse event C1276127 Sporadic porphyria cutanea tarda MalaCards C0012569 Double vision C0270932 Neuropathy paraneoplastic HSDN C0038002 Spleen enlargement C1720860 Familial partial lipodystrophy, type 2 HPO C0015402 Hemorrhage eye C0020302 Hydrophthalmos HSDN C0262384 Chest pain atypical C0011581 Depressive disorder UMLS C0151825 Ostalgia C0006142 Malignant neoplasm of breast UMLS C0042510 Fibrillation paroxysmal vent C2673193 Brugada syndrome 2 MalaCards|HPO C0085631 Abnormal excitement C0276496 Familial alzheimer disease (fad) MalaCards C0399593 Parotid sialectasia C0012359 Pathological dilatation UMLS C2203646 Jaundice C0314657 Genetic predisposition HSDN C0542476 Forgetful C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0018681 Headache, cephalalgia C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0018784 Deafness sensorineural C0003855 Arteriovenous fistula HSDN C4084769 Vomiting frequency C0026782 Mumps vaccine HSDN C0018991 Paralysis one side of body C0338586 Vertebral artery dissection HSDN C0018784 Deafness sensorineural C0282644 Smith-lemli-opitz syndrome, type ii MalaCards C0020305 Fetal edema C0268228 Neuraminidase 1 deficiency OrphaNet|HPO C0018784 Deafness sensorineural C1832812 Cataracts, congenital, with sensorineural deafness, down syndrome-like facial appearance, short stature, and mental retardation HPO C0037317 Sleep disturbance C2931902 Acute brachial neuritis MalaCards C0038002 Spleen enlargement C1704429 Hypoalphalipoproteinemia, familial OrphaNet|HPO|MalaCards C0151908 Dry skin C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards C2919142 Short stature adverse event C2363065 Vitamin d-resistant rickets OrphaNet|MalaCards C0155552 Hearing loss mixed C1956418 Torsion abnormality HSDN C4085222 Nausea C0001403 Addison disease HSDN C1963137 Hydrocephalus adverse event C1332140 Acrofacial dysostosis MalaCards C4084788 Have dizziness C0752160 Hemangioma, cavernous, central nervous system HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033677 Protein-energy malnutrition HSDN C0012833 Dizzy C0271488 Active meniere's disease, nos UMLS C0023014 Developmental disorder language C0700639 Pyloric stenosis, hypertrophic HSDN C0018681 Headache, cephalalgia C0702166 Acne HSDN C0033774 Skin pruritus C0037274 Dermatologic disorders UMLS C1384666 Decreased hearing C2931649 Larsen syndrome, recessive type MalaCards C0231218 Malaise generalized C0854836 Angiocentric lymphoma stage ii UMLS C3539896 Pelvic pain occurs with urination C0007621 Neoplastic cell transformation HSDN C0015300 Ocular proptosis C0265344 Donohue syndrome OrphaNet|HPO C0036572 Convulsion C0009088 Cluster headache HSDN C2237041 Shox gene with short stature C1849193 Peeling skin syndrome MalaCards|HPO C0012833 Dizzy C0039590 Testicular neoplasms HSDN C4084776 Weight loss C0037929 Spinal cord injuries HSDN C0015230 Exanthem C0406314 Psoriasis geographica UMLS C0040034 Thrombocytopenia C0398691 Hyperimmunoglobulinemia d MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0003469 Anxiety disorders HSDN C4084784 Diarrhea C0947622 Cholecystolithiasis HSDN C3887638 Failure to thrive in infant C0268417 Pancreatic trypsinogen deficiency MalaCards C2984057 Have nausea C0032087 Plant poisoning HSDN C0851578 Disorder sleep C0033922 Psychomotor disorders MalaCards C4085211 Pain distress question C0029184 Orbital fracture HSDN C0002962 Angina C0265326 Bannayan-riley-ruvalcaba syndrome MalaCards|HPO C0040822 D tremors C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant OrphaNet|HPO C0474368 Childbirth pain C3542996 Mindfulness HSDN C4049602 Hyperactivity C0796241 Mental retardation, x linked 34 (disorder) HPO C0518090 Frequency of pain question C1963084 Colitis adverse event HSDN C4084773 Bothered by weight gain C0024841 Matrimony, matrimonial HSDN C0812426 Kidney problem C0035078 Kidney failure UMLS C4042891 Sleep wake disorders C0019080 Hemorrhage HSDN C0024032 Birth weight subnormal C0008626 Congenital chromosomal disease MalaCards C3815497 Cough C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0020305 Fetal edema C0003873 Rheumatoid arthritis HSDN C0349588 Stature short C1832162 Hypotrichosis, congenital, with juvenile macular dystrophy OrphaNet|HPO|MalaCards C0010038 Corneal opacity disorder C0270612 Leukoencephalopathies MalaCards C1963170 Hypothermia adverse event C0025284 Meningeal neoplasms HSDN C0020672 Body temperature decreased C0034067 Pulmonary emphysema HSDN C0018681 Headache, cephalalgia C0752182 Central nervous system protozoal infections HSDN C0497247 Blood pressure elevation C2931253 Alport syndrome, dominant type MalaCards C0003962 Ascites C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C4084774 Have weight loss C1253937 Pericardial effusion HSDN C2984057 Have nausea C0009088 Cluster headache HSDN C1069915 Vertigo C0812393 Cancer patients and suicide and depression HSDN C4084784 Diarrhea C0024810 Marijuana smoking HSDN C1557397 Adverse event associated with pain C1691228 Cystic kidney diseases HSDN C0018989 Paresis of one side of body C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0036572 Convulsion C0268529 Proline dehydrogenase deficiency MalaCards|HPO|UMLS C2984058 Have pain C0019364 Herpes zoster ophthalmicus HSDN C4050613 Anxiety C0342200 Endemic cretinism MalaCards C0022346 Yellow skin C0002871 Anemia UMLS C1963071 Back pain adverse event C0025284 Meningeal neoplasms MalaCards C4020887 Photodysphoria C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0026838 Spasticity muscle C2936910 Cross-mckusick-breen syndrome OrphaNet|MalaCards C4084784 Diarrhea C0574960 Sacroiliitis HSDN C0020672 Body temperature decreased C0016542 Foreign body HSDN C4084784 Diarrhea C0302280 Adrenogenital syndrome HSDN C3541349 Syncope C0029463 Osteosarcoma HSDN C4084723 Constipation C0036341 Schizophrenia HSDN C2919142 Short stature adverse event C1835009 Mesomelic dysplasia, kantaputra type OrphaNet|MalaCards C0024032 Birth weight subnormal C0175692 Johanson-blizzard syndrome MalaCards|HPO C0013404 Respiratory difficulty C2350019 Solitary pulmonary nodule HSDN C0018777 Deafness, conductive C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0007134 Renal cell carcinoma HSDN C1961131 Cough adverse event C0080107 Fistula, respiratory tract HSDN C3539023 Pelvic pain increasing in frequency C0019066 Nontraumatic hemoperitoneum HSDN C0015970 Fever unknown origin C0019104 Hemorrhagic fevers, viral HSDN C2315100 Pediatric failure to thrive C1969084 Pontocerebellar hypoplasia type 6 MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0079731 B-cell lymphomas HSDN C0013362 Dysarthrias C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C0040264 Ear ringing sound C0007137 Squamous cell carcinoma HSDN C0042025 Urinary incontinence stress C0038661 Suicide HSDN C3641756 Have diarrhea C0007762 Cerebellar neoplasms HSDN C4085210 Usual severity pain C0037305 Neoplasm, skull HSDN C0015469 Facial paralysis C0038395 Streptococcal infections HSDN C0013404 Respiratory difficulty C0085179 Eosinophilia-myalgia syndrome HSDN C3539022 Pelvic pain decreasing in severity C0007527 Cecal disease HSDN C0151786 Weakness muscle C0024228 Lymphatic diseases HSDN C4084773 Bothered by weight gain C3495801 Granulomatosis with polyangiitis HSDN C3815497 Cough C0019655 Histoplasmosis HSDN C0751837 Gait ataxic C0393665 Multiple sclerosis, chronic progressive HSDN C0028961 Urine output decreased C0036980 Shock, cardiogenic HSDN C2024893 Cardiovascular surgery result: fatigue C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0027497 Queasy C0011127 Pressure ulcer HSDN C0011168 Disorder deglutition C1864996 Enteric neuropathy, familial MalaCards C0020672 Body temperature decreased C0796561 Melanoma vaccines HSDN C1962972 Proteinuria adverse event C0029294 Orofaciodigital syndromes MalaCards C0413252 Hypothermia due to exposure C0342200 Endemic cretinism MalaCards C1961131 Cough adverse event C0027746 Nerve degeneration HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020640 Inherited factor ii deficiency HSDN C0003469 Anxiety disorder C0270972 Cornelia de lange syndrome OrphaNet|HPO|MalaCards C0557874 Global developmental delay C1849088 Spinocerebellar ataxia with dysmorphism OrphaNet C0031911 Pigment deposition C1305256 Angiolipoma, infiltrating MalaCards C4085661 Usual severity nausea C0004933 Behavior modification technique HSDN C3463815 Feel fatigue C1547046 Kind of quantity - taste HSDN C0557874 Global developmental delay C1832588 Chromosome 11p11.2 deletion syndrome OrphaNet|HPO|MalaCards C0424810 Periorbital swelling C4012050 Hennekam lymphangiectasia-lymphedema syndrome 1 MalaCards C0427055 Face weakness C0410179 Scleroatonic muscular dystrophy MalaCards|HPO C0009806 Constipate C0019360 Herpes zoster disease HSDN C4085210 Usual severity pain C0162872 Aortic aneurysm, thoracic HSDN C4084726 Distress cough C0524909 Hepatitis b, chronic HSDN C4084802 Usual severity diarrhea C0006625 Cachexia HSDN C0036572 Convulsion C0004352 Autistic disorder HSDN|HPO C3146279 Coma C1556061 Electric injuries HSDN C0016199 Pain flank C0085096 Peripheral vascular diseases HSDN C0150055 Pain chronic C0024299 Lymphoma HSDN C0003910 Articulation disorder C0152181 Hypoglossal nerve disease or syndrome HSDN C1961131 Cough adverse event C0030424 Paragonimiasis HSDN C0151740 Intracranial hypertension C0023788 Whipple disease MalaCards C0037383 Sneeze C0271375 Cranial nerve palsy iv trochlear HSDN C0575081 Abnormal gait C0018523 Hallervorden-spatz syndrome OrphaNet|HPO|MalaCards C0007859 Pain neck C0206642 Parosteal osteosarcoma HSDN C3463815 Feel fatigue C0027663 Neoplasms, multiple primary HSDN C0332563 Papulae C0852007 Scleroderma and associated disorders OrphaNet C0151908 Dry skin C0162359 Christ-siemens-touraine syndrome OrphaNet|UMLS|HPO|MalaCards C4085222 Nausea C0002878 Anemia, hemolytic HSDN C1549543 Administration method - pain C0007020 Carbon monoxide poisoning HSDN C1579931 Depressed - symptom C0017205 Gaucher disease OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0033871 Psychiatric status rating scales HSDN C0018772 Deafness C1555914 Psychologist - psychotherapy, group HSDN C0234992 Dyskinesia acute C0013384 Dyskinetic syndrome UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0518449 Control of hip fracture risk HSDN C0007166 Cardiac output decreased C0460137 Push down or depress HSDN C0349588 Stature short C1851412 Extrasystoles, multiform ventricular, with short stature, hyperpigmentation and microcephaly OrphaNet|MalaCards C3539892 Pelvic pain in front C0006118 Brain neoplasms HSDN C0427190 Ataxia, truncal C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C1565249 Limitation, mobility C0009940 Convalescence HSDN C1963249 Tinnitus adverse event C0007279 Carotid body paraganglioma HSDN C0005745 Blepharoptosis C0796274 Brown-vialetto-van laere syndrome OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0005745 Blepharoptosis HSDN C0018772 Deafness C0460137 Push down or depress HSDN C0278152 Hemifacial spasms C0752155 Central nervous system vascular malformations HSDN C0424755 Fever symptoms C0085096 Peripheral vascular diseases HSDN C3898969 Have been vomiting C0001807 Aggressive behavior HSDN C4085661 Usual severity nausea C0600564 Self-efficacy HSDN C1963093 Dizziness adverse event C0027531 Neck injury HSDN C0043144 Wheeze C1260881 Allergic bronchitis UMLS C0522224 Palsied C0001173 Adult pyloric stenosis HSDN C0020796 Profoundly mentally retarded C3150413 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 MalaCards|HPO C0398650 Idiopathic thrombocytopenia purpura C1863236 Scid due to ada deficiency, early-onset HPO C0009398 Color vision defects C1706377 Memory device component HSDN C0019572 Hairiness C1623041 Breast-fed HSDN C0030975 Disorders perception C0015674 Chronic fatigue syndrome HSDN C4084769 Vomiting frequency C3539923 Cdisc adas-cog - orientation summary score HSDN C0004604 Pain back C0039614 Tetanus HSDN C0015469 Facial paralysis C1962979 Burn adverse event HSDN C2919142 Short stature adverse event C1848410 Xeroderma pigmentosum, variant type MalaCards C1557397 Adverse event associated with pain C0019151 Hepatic encephalopathy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0521585 Gastrointestinal mucositis HSDN C0037317 Sleep disturbance C0175693 Russell-silver syndrome MalaCards C3898969 Have been vomiting C0276386 Mosquito-borne viral fever, oropouche MalaCards C2126412 Pain in left forearm C0810058 Other connective tissue disease UMLS C0150055 Pain chronic C0520946 Emotional hypersensitivity HSDN C0151786 Weakness muscle C0021141 Inappropriate adh syndrome HSDN C0178417 Anhedonia C0525045 Mood disorders HSDN C0038990 Sweats C0079299 Epidermolysis bullosa simplex kobner OrphaNet|HPO C0263629 Tumor-like lesions of the skin C0221269 Pseudolymphoma UMLS C2984058 Have pain C0016879 Fusobacterium infections HSDN C0150055 Pain chronic C0002395 Alzheimer's disease HSDN C0027497 Queasy C0031511 Pheochromocytoma MalaCards C0020673 Hypothermia (central) (local) C1412124 Acls gene HSDN C2128731 Mid left leg soft tissue swelling C0037580 Soft tissue swelling UMLS C2024878 Cardiovascular surgery result: dyspnea C3813607 Infantile gastroesophageal reflux HSDN C0030193 Sense of pain C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C3539889 Pelvic pain increasing in severity C0034888 Rectal prolapse HSDN C1579931 Depressed - symptom C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C0003467 Angst C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0221752 Rbc urine C1857389 Cystinuria, type b MalaCards C4084776 Weight loss C0080179 Vertebra fracture HSDN C0850758 Pain pelvic C0010356 Cross infection HSDN C0011991 Loose stools C0036231 Sarcocystosis DiseaseOntology C3641755 Have constipation C0007133 Carcinoma, papillary HSDN C0518090 Frequency of pain question C0028879 Odontogenic cysts HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0751967 Multiple sclerosis, relapsing-remitting HSDN C0011991 Loose stools C2242987 Benign mastocytoma MalaCards C0022346 Yellow skin C0007112 Adenocarcinoma of prostate UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0030583 Parotitis HSDN C3887873 Hearing loss C0026769 Multiple sclerosis HSDN C1279888 Proteinuria of undiagnosed cause C0007682 Cns disorder HSDN C0030193 Sense of pain C0423738 Levator syndrome UMLS C4084773 Bothered by weight gain C0027697 Nephritis HSDN C0008031 Pain chest C0035956 Rupture spontaneous HSDN C4084784 Diarrhea C2711227 Steatohepatitis HSDN C0018991 Paralysis one side of body C0220981 Metabolic acidosis HSDN C1963087 Constipation adverse event C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C1384666 Decreased hearing C0850803 Anaphylaxis (non medication) HSDN C0042928 Paralysis vocal cord C0751799 Brain hemorrhage, traumatic HSDN C0085593 Chill C0473876 Cryptogenic tularaemia MalaCards C4084769 Vomiting frequency C1522133 High cholesterol level HSDN C0151825 Ostalgia C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C4085661 Usual severity nausea C0011849 Diabetes mellitus HSDN C0036572 Convulsion C0004782 Basal ganglia diseases HSDN C0011991 Loose stools C0007798 Cerebral ventricle neoplasm HSDN C0242936 Center pain C1963215 Pneumothorax adverse event HSDN C4084767 Bothered by vomiting C2706915 Language:-:point in time:^patient:- HSDN C4084769 Vomiting frequency C0022593 Keratosis HSDN C0043094 Weight gain C0033839 Pseudorabies HSDN C0038002 Spleen enlargement C1856492 Gaucher disease, type iiib HPO C3812171 Bradycardia by ecg finding C1563716 Thyroid dysgenesis HPO C0004604 Pain back C0034065 Pulmonary embolism HSDN C0040034 Thrombocytopenia C0206624 Hepatoblastoma MalaCards C1963252 Tremor adverse event C0024117 Chronic obstructive airway disease HSDN C0030552 Paralysis partial C0007771 Intracranial arteriosclerosis HSDN C1279888 Proteinuria of undiagnosed cause C1253943 Fluid in the chest HSDN C4085317 Diarrhea frequency C0001139 Acinetobacter infection HSDN C0002965 Crescendo angina C2240374 Eosinophil count raised HSDN C1557397 Adverse event associated with pain C0030925 Peptic ulcer with penetration HSDN C0027796 Neuralgias C0037369 Smoking HSDN C2315100 Pediatric failure to thrive C3151482 Hypercalciuria, childhood, self-limiting HPO C3146279 Coma C0006663 Calcinosis HSDN C1868756 Corneal leucoma C1265876 Opacities UMLS C0241210 Speaking delay C0268151 Classical galactosemia MalaCards C0030193 Sense of pain C0030354 Papilloma HSDN C0042571 Vertigo subjective C0242698 Ventricular dysfunction, left HSDN C0019572 Hairiness C2030274 Heavy bleeding between periods HSDN C0917816 Deficiency mental C1845672 Mental retardation, x-linked 63 HPO C0018989 Paresis of one side of body C0162309 Adrenoleukodystrophy OrphaNet|MalaCards C3887638 Failure to thrive in infant C0020621 Hypokalemia HSDN C0019825 Voice hoarseness C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C2911645 Weight loss adverse event C0023051 Laryngeal diseases HSDN C2911645 Weight loss adverse event C0036983 Septic shock HSDN C2187990 Unable to perform sex C0268407 Senile cardiac amyloidosis MalaCards C0424755 Fever symptoms C0001752 African swine fever HSDN C1557397 Adverse event associated with pain C1136321 Hiv-associated lipodystrophy syndrome HSDN C4085548 Usual severity dizziness C0009946 Conversion disorder HSDN C3665492 Pigmentations C1864205 Macular degeneration, age-related, 1 MalaCards C0242936 Center pain C0008732 Chylous ascites HSDN C0518090 Frequency of pain question C0023524 Leukoencephalopathy, progressive multifocal HSDN C4084774 Have weight loss C0062527 Hepatitis b vaccine HSDN C0036572 Convulsion C0019625 Sinus histiocytosis MalaCards C1000483 Genus anemia C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0041952 Uerterolithiasis HSDN C0015230 Exanthem C0035865 Disease rivers ross MalaCards C1384666 Decreased hearing C0022865 Obstetric labor complications HSDN C0019079 Bloody sputum C1708781 Lung sarcomatoid carcinoma UMLS C4084768 Usual severity vomiting C0003850 Arteriosclerosis HSDN C0007166 Cardiac output decreased C0013274 Patent ductus arteriosus HSDN C4084723 Constipation C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C2029884 Hearing loss by exam C0032963 Pregnancy complications, cardiovascular HSDN C0036572 Convulsion C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C0036572 Convulsion C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C2919142 Short stature adverse event C4014435 Mental retardation, autosomal dominant 26 MalaCards C4085317 Diarrhea frequency C1962976 Ventricular fibrillation adverse event HSDN C3539893 Pelvic pain occurs with intercourse C0017181 Gastrointestinal hemorrhage HSDN C0454644 Delayed language development C1857802 Morm syndrome HPO C1963252 Tremor adverse event C0020443 Hypercholesterolemia HSDN C0003862 Pain joint C0017181 Gastrointestinal hemorrhage HSDN C0026838 Spasticity muscle C3150171 Ftld-tdp, tardbp-related HPO C1963091 Diarrhea adverse event C0019195 Hepatitis, viral, human HSDN C3539890 Pelvic pain causes awakening at night C0019553 Contracture hips HSDN C1962972 Proteinuria adverse event C0000735 Abdominal neoplasms HSDN C0013404 Respiratory difficulty C0027932 Neurotic disorders HSDN C0015469 Facial paralysis C0037036 Sialorrhea HSDN C0522224 Palsied C0020649 Hypotension HSDN C4085210 Usual severity pain C0919691 Anastomotic leaks HSDN C1962972 Proteinuria adverse event C0009241 Cognition disorders HSDN C4085549 Dizziness C0000833 Abscess HSDN C3815497 Cough C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0030486 Extremity paralysis, lower C0000771 Abnormalities, drug induced HSDN C0030486 Extremity paralysis, lower C0524620 Metabolic syndrome x HSDN C0518090 Frequency of pain question C0038017 Congenital spondylolisthesis HSDN C0013421 Dystonia C0699828 Serotonergic syndrome HSDN C4084723 Constipation C0003493 Aortic diseases HSDN C0474368 Childbirth pain C0004361 Autogenic therapy HSDN C0022346 Yellow skin C0005411 Biliary atresia MalaCards|UMLS C0040822 D tremors C1961100 Erectile dysfunction adverse event HSDN C2203646 Jaundice C0086543 Cataract nos HSDN C0038506 Stutter C0016989 Galvanic skin response HSDN C4085862 Bothered by nausea C1866552 Paragangliomas 2 (disorder) MalaCards C0022638 Ketosis C0342337 Insulin resistance syndrome, type b MalaCards C0151786 Weakness muscle C0497552 Congenital neurologic anomalies HSDN C0036396 Sciatica C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4085661 Usual severity nausea C0079774 Peripheral t-cell lymphoma HSDN C1557397 Adverse event associated with pain C1963139 Hypopigmentation adverse event HSDN C0018681 Headache, cephalalgia C0007863 Occipital neuralgia UMLS C1384666 Decreased hearing C0007786 Brain ischemia HSDN C0027796 Neuralgias C0848377 Trauma to the abdomen HSDN C0557874 Global developmental delay C2931370 Bilateral ulnar hypoplasia and mental retardation MalaCards C0019079 Bloody sputum C0003490 Aortic arch syndrome MalaCards|HSDN C0424755 Fever symptoms C0040820 Trematode infections HSDN C4084788 Have dizziness C0039614 Tetanus HSDN C0018772 Deafness C0009917 Contracture HSDN C0010520 Skin cyanosis C0026764 Multiple myeloma HSDN C4085317 Diarrhea frequency C3814530 Skin vesicle HSDN C1000483 Genus anemia C1859407 Bone dysplasia, lethal, holmgren type MalaCards C0234428 Consciousness disturbance C0011206 Delirium UMLS C0005745 Blepharoptosis C3266898 Waardenburg syndrome MalaCards C0151315 Neck rigid C0152998 Acute nonparalytic poliomyelitis, poliovirus, unspecified type DiseaseOntology|MalaCards C3665346 Loss sight C1837713 Joubert syndrome 3 MalaCards C4085211 Pain distress question C0024899 Mastocytosis HSDN C1971624 Appetite absent C0001175 Acquired immunodeficiency syndrome HSDN C3641756 Have diarrhea C0007193 Cardiomyopathy, dilated HSDN C0000731 Abdomen distention C3661523 Congenital intestinal aganglionosis MalaCards C1963071 Back pain adverse event C1269683 Major depressive disorder HSDN C0042024 Urine incontinence C0019080 Hemorrhage HSDN C1963137 Hydrocephalus adverse event C1859487 Biemond syndrome ii MalaCards C4084723 Constipation C3244301 Coverage level - family HSDN C4084769 Vomiting frequency C3714644 Thymus neoplasms HSDN C0030193 Sense of pain C1253943 Fluid in the chest HSDN C4084726 Distress cough C1000483 Genus anemia HSDN C0000737 Abdomen pain C0004659 Bacteriuria HSDN C0727671 Red cross toothache drops C0406810 Carney complex HSDN C0013144 Drowsy C0014054 Biundulant milk fever DiseaseOntology|MalaCards C0018784 Deafness sensorineural C2751320 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay MalaCards|HPO C0518090 Frequency of pain question C4041080 Neurocognitive disorders HSDN C2203646 Jaundice C0034885 Rectal neoplasms HSDN C4084767 Bothered by vomiting C0027659 Neoplasms, experimental HSDN C4084769 Vomiting frequency C0018021 Goiter HSDN C4084775 Usual severity weight loss C0042251 Vaginal diseases HSDN C1145670 Failure respiratory C0175691 Dubowitz syndrome OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0439840 Reflex motion descriptor HSDN C2024893 Cardiovascular surgery result: fatigue C0002880 Autoimmune hemolytic anemia OrphaNet C1557397 Adverse event associated with pain C0014009 Empyema HSDN C3274924 Have been coughing C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084726 Distress cough C0036329 Schistosomiasis japonica DiseaseOntology C0522224 Palsied C0149514 Bronchitis acute HSDN C4084776 Weight loss C0039231 Tachycardia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0007097 Carcinomas HSDN C1962972 Proteinuria adverse event C0848548 Hypertensive nephropathy MalaCards C0022346 Yellow skin C0032787 Postoperative complications HSDN C0009792 Consciousness disorder C0004377 Automatism HSDN C4085210 Usual severity pain C1963090 Dehydration adverse event HSDN C0037036 Increased salivation C0796237 Mental retardation, x-linked 30 HPO C0000737 Abdomen pain C0007134 Renal cell carcinoma HSDN C4084784 Diarrhea C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards C0344232 Blurred vision C1719788 Episodic ataxia type 1 HPO C0585542 Bppv - benign paroxysmal positional vertigo nystagmus C1290841 Acute disease of nervous system UMLS C0427202 Atony, muscular C0267175 Nondiabetic gastroparesis UMLS C2984058 Have pain C0035412 Rhabdomyosarcoma HSDN C0424755 Fever symptoms C0010043 Corneal ulcer HSDN C1961131 Cough adverse event C1761609 Aspiration pneumonitis MalaCards C0020455 Hypergammaglobulinemia C1540912 Hypereosinophilic syndrome HSDN C0030552 Paralysis partial C2963140 Arteriovenous fistula in use with two needles HSDN C4049644 Depression C3160718 Parkinson disease, late-onset MalaCards|HPO C1962972 Proteinuria adverse event C0392525 Nephrolithiasis HSDN C4084725 Usual severity cough C0149721 Left ventricular hypertrophy HSDN C3641756 Have diarrhea C0025345 Menstruation disturbances HSDN C2203646 Jaundice C0013922 Embolism HSDN C0015970 Fever unknown origin C0030328 Panniculitis, nodular nonsuppurative HSDN C1384666 Decreased hearing C0035801 Diseases rodent HSDN C1145670 Failure respiratory C0035436 Rheumatic fever MalaCards C0476250 Head neck mass C1563142 Hamartoma of retina UMLS C1963281 Vomiting adverse event C0033871 Psychiatric status rating scales HSDN C4084774 Have weight loss C0027819 Neuroblastoma MalaCards|HSDN C4085862 Bothered by nausea C1135841 Zoster sine eruptione HSDN C1260880 Nasal drip C3897737 Recurrent inverted schneiderian papilloma UMLS C4084784 Diarrhea C1837329 Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema MalaCards C0003467 Angst C0751435 Hyperphenylalaninaemia MalaCards C4084774 Have weight loss C0009917 Contracture HSDN C0004134 Dyssynergia C1859570 Bardet-biedl syndrome 12 HPO C0015676 Mental fatigue C0021432 Infratentorial neoplasms HSDN C0518090 Frequency of pain question C0024899 Mastocytosis HSDN C0013404 Respiratory difficulty C2186740 Reported urticaria HSDN C4020887 Photodysphoria C1274795 Urban schosser spohn syndrome OrphaNet|MalaCards C3274924 Have been coughing C0022408 Arthropathy HSDN C4084767 Bothered by vomiting C0038013 Ankylosing spondylitis HSDN C0522224 Palsied C0009241 Cognition disorders HSDN C2984058 Have pain C0812470 Abortion, incomplete HSDN C0030193 Sense of pain C0877792 Sleep disorders, circadian rhythm HSDN C1963093 Dizziness adverse event C1956346 Coronary artery disease HSDN C4084774 Have weight loss C0036439 Scoliosis, unspecified HSDN C0018524 Hallucinate C2349049 Unit of infective dose HSDN C0040460 Dental pain C1999266 Depression adverse event HSDN C4085317 Diarrhea frequency C0006277 Bronchitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030186 Paget disease extramammary HSDN C0015230 Exanthem C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C3814778 Hemolytic index HSDN C3541349 Syncope C0026771 Trauma multiple HSDN C1549543 Administration method - pain C0036421 Systemic scleroderma HSDN C3274924 Have been coughing C0236969 Substance-related disorders HSDN C0036572 Convulsion C0600041 Infective cystitis HSDN C0013395 Indigestion C1550672 Specimen type - ulcer HSDN C0039870 Leanness C0009404 Colorectal neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0036202 Sarcoidosis OrphaNet|HSDN|HPO|MalaCards C4084775 Usual severity weight loss C0031350 Pharyngitis HSDN C3887784 Decreased urine output C0031190 Persistent fetal circulation syndrome HSDN C0332563 Papulae C0281479 Primary systemic amyloidosis MalaCards C0042798 Vision dim C0012979 Canine disease HSDN C0003467 Angst C0796237 Mental retardation, x-linked 30 HPO C0027497 Queasy C0002736 Amyotrophic lateral sclerosis HSDN C0231218 Malaise generalized C0849867 Disease;generalised UMLS C3463815 Feel fatigue C3888018 Congenital hyperinsulinism MalaCards C0013604 Edematous C0242216 Biliary calculi HSDN C0917816 Deficiency mental C0265961 Erythrokeratodermia variabilis HPO C0009080 Finger clubbing C1279945 Acute interstitial pneumonia MalaCards C0015732 Feces incontinence C0342623 Senile systemic amyloidosis MalaCards C1290644 Extrinsic staining of teeth associated with oral habits C0553565 Posteruptive teeth stain. nos UMLS C0012569 Double vision C1720416 Episodic ataxia type 2 (disorder) MalaCards|HPO C0232461 Increased appetite C3809844 Chromosome 22q13 duplication syndrome MalaCards C4084774 Have weight loss C0018099 Gout HSDN C0007758 Cerebellar ataxia C0029456 Osteoporosis HSDN C1971624 Appetite absent C0085399 Ehrlichiosis HSDN C4084724 Usual severity constipation C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0239591 Finger paresthesia C0030554 Paresthesia UMLS C0043094 Weight gain C0497327 Dementia HSDN C2911647 Weight gain adverse event C0036239 Satiety HSDN C4084774 Have weight loss C1848814 Thymoma, familial MalaCards C2055364 Temporary loss of urinary control with physical exercise C0042024 Urinary incontinence UMLS C0003811 Cardiac rhythm disturbance C0085298 Sudden cardiac death MalaCards C0152459 Striae C0233315 Premature birth of newborn HSDN C0518090 Frequency of pain question C0039263 Takayasu arteritis HSDN C4084788 Have dizziness C0919267 Ovarian neoplasm HSDN C0011206 Delirium acute C1090821 Sepsis (invertebrate) HSDN C0020450 Hyperemesis gravidarum C0018801 Heart failure HSDN C0150055 Pain chronic C0700327 Clinical findings relating to memory HSDN C4084726 Distress cough C0206703 Carcinoma, giant cell HSDN C0013395 Indigestion C0037933 Spinal diseases HSDN C0518090 Frequency of pain question C0085409 Polyendocrinopathies, autoimmune HSDN C2911645 Weight loss adverse event C0011303 Demyelinating diseases HSDN C4084767 Bothered by vomiting C0007099 Carcinoma in situ HSDN C0042798 Vision dim C1527406 Rhizomelic pseudopolyarthritis MalaCards C0151786 Weakness muscle C1833373 Inclusion body myopathy, autosomal recessive MalaCards C4084774 Have weight loss C0006840 Candidiasis HSDN C0040460 Dental pain C0037369 Smoking HSDN C0018681 Headache, cephalalgia C1861451 Stormorken syndrome MalaCards|UMLS C0010520 Skin cyanosis C0039445 Hereditary hemorrhagic telangiectasia HPO|UMLS C2919142 Short stature adverse event C0036996 Short rib-polydactyly syndrome MalaCards C0030193 Sense of pain C0263894 Paralytic sciatica UMLS C0007758 Cerebellar ataxia C0042029 Urinary tract infection HSDN C2096293 Ent surgical result ear vertigo C0264766 Rheumatic mitral stenosis HSDN C3887638 Failure to thrive in infant C0205710 Alpers syndrome (disorder) MalaCards|HPO C0042024 Urine incontinence C1836916 Posterior column ataxia with retinitis pigmentosa HPO C4085211 Pain distress question C0013502 Echinococcosis HSDN C0030193 Sense of pain C0752143 Intracranial thrombosis HSDN C4084784 Diarrhea C0042994 Vulvar diseases HSDN C4085211 Pain distress question C0003868 Arthritis, gouty HSDN C0036572 Convulsion C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C0162323 Arthritis, multiple joint involvement C0036202 Sarcoidosis MalaCards C2024878 Cardiovascular surgery result: dyspnea C0206063 Radiation pneumonitis HSDN C4084726 Distress cough C0017160 Gastroenteritis HSDN C0013404 Respiratory difficulty C0004935 Animal ethology HSDN C0518090 Frequency of pain question C0001422 Adenofibroma HSDN C0042510 Fibrillation paroxysmal vent C3501851 Long qt syndrome 2-5 MalaCards C0542476 Forgetful C0022336 Creutzfeldt-jakob disease MalaCards|HPO C0018784 Deafness sensorineural C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C3887638 Failure to thrive in infant C1857563 Hsd11b2, tyr299del HPO C0036572 Convulsion C1861129 Takao vcf syndrome HPO C0016382 Cutaneous vascular engorgement C0010495 Cutis laxa MalaCards C3665347 Vision impaired C0008029 Cherubism MalaCards|HPO C3887638 Failure to thrive in infant C3150921 Microcephaly, postnatal progressive, with seizures and brain atrophy HPO C3539891 Pelvic pain to the rear C0023895 Liver diseases HSDN C0018784 Deafness sensorineural C0268238 Triglyceride storage disease with ichthyosis MalaCards|HPO C0040822 D tremors C0003869 Arthritis, infectious HSDN C1963063 Anorexia adverse event C0041313 Hepatic tuberculosis DiseaseOntology|MalaCards C3887638 Failure to thrive in infant C1563706 Nephrogenic diabetes insipidus, type ii HPO C4042891 Sleep wake disorders C0017638 Glioma HSDN C1557397 Adverse event associated with pain C0004044 Asphyxia HSDN C0002624 Amnesia retrograde C4085311 Depression - recess HSDN C0004134 Dyssynergia C0022665 Kidney neoplasm HSDN C0242936 Center pain C0206504 Tympanic membrane perforation HSDN C2315100 Pediatric failure to thrive C0425045 Sudden infant death HSDN C0000737 Abdomen pain C1963274 Vasculitis adverse event HSDN C0018784 Deafness sensorineural C2608080 Renal hypoplasia, isolated (disorder) HPO C4084774 Have weight loss C0020598 Hypocalcemia HSDN C0016382 Cutaneous vascular engorgement C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0150045 Urinary incontinence urge C0004659 Bacteriuria HSDN C3203358 Alveolar hypoventilation C0022665 Kidney neoplasm HSDN C0013604 Edematous C0015927 Intrauterine fetal demise HSDN C4085210 Usual severity pain C0014356 Enterocolitis HSDN C2919142 Short stature adverse event C0086438 Hypogammaglobulinemia MalaCards C4084784 Diarrhea C0023240 Legionellosis MalaCards C0497406 Over weight C0344434 Atrial fibrillation ecg HSDN C0085642 Asphyxia reticularis C0030489 Paraproteinemias HSDN C0030193 Sense of pain C0033117 Priapism HSDN C4084767 Bothered by vomiting C0023473 Myeloid leukemia, chronic HSDN C3463815 Feel fatigue C0035127 Cumulative trauma disorders HSDN C0018808 Murmur C0007095 Carcinoid tumor MalaCards C4084773 Bothered by weight gain C0006277 Bronchitis HSDN C0018681 Headache, cephalalgia C0036323 Schistosomiasis HSDN C0494475 Seizure generalized tonic clonic C1846648 Microcephaly, amish type (disorder) MalaCards|HPO C0040485 Wryneck C0856068 Torticollis aggravated UMLS C3887873 Hearing loss C0001969 Alcoholic intoxication HSDN C0036572 Convulsion C3809420 Cortical dysplasia, complex, with other brain malformations 4 MalaCards|UMLS C0019209 Large liver C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards C4085222 Nausea C0018794 Heart block HSDN C1279888 Proteinuria of undiagnosed cause C1850510 Sialidosis, type i HPO C0041657 Consciousness loss C0025427 Mercury poisoning OrphaNet|MalaCards C0019209 Large liver C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|HPO|MalaCards C0039870 Leanness C0004238 Atrial fibrillation HSDN C0332563 Papulae C1866398 Proteus-like syndrome (disorder) MalaCards C1961131 Cough adverse event C0038356 Stomach neoplasms HSDN C0024032 Birth weight subnormal C0432442 Chromosome 18p deletion syndrome MalaCards C0015672 Decreased energy C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0751837 Gait ataxic C1856689 Friedreich ataxia 1 HPO C0011991 Loose stools C0221056 Adult type dermatomyositis HSDN C0011570 Monopolar depression C0795953 Masa syndrome (disorder) MalaCards C3873425 Autoimmune xerostomia C0043352 Xerostomia UMLS C0024031 Back pain lower back C0007130 Mucinous adenocarcinoma HSDN C0012833 Dizzy C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C0041657 Consciousness loss C0011253 Delusions HSDN C0018784 Deafness sensorineural C0016719 Friedreich ataxia HSDN C4084774 Have weight loss C0004935 Animal ethology HSDN C2919142 Short stature adverse event C0265336 Senter syndrome MalaCards|HPO C1549543 Administration method - pain C0005935 Bone conduction HSDN C3146279 Coma C0042338 Herpesvirus 3, human HSDN C0012833 Dizzy C1134719 Invasive ductal breast carcinoma HSDN C1963252 Tremor adverse event C1962983 Cataract adverse event HSDN C1313921 Urinomas C0042021 Urinary fistula HSDN C3146279 Coma C0020473 Hyperlipidemia HSDN C4084773 Bothered by weight gain C0040136 Thyroid neoplasm HSDN C0086437 Joint hypermobility C3151218 Osteogenesis imperfecta, type xi MalaCards|UMLS C4084724 Usual severity constipation C0079744 Diffuse large b-cell lymphoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1962962 Hyperpigmentation adverse event HSDN C4084727 Cough frequency C0009651 Conditioning operant HSDN C4085211 Pain distress question C0001422 Adenofibroma HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0023176 Lead poisoning HSDN C0027497 Queasy C0024636 Malocclusion HSDN C4049644 Depression C0268322 Chester-type porphyria HPO C0013362 Dysarthrias C1847967 Ovarioleukodystrophy MalaCards|HPO C4084767 Bothered by vomiting C0085277 Munchausen by proxy syndrome HSDN C2984058 Have pain C0035321 Retinal tear HSDN C0015672 Decreased energy C1306794 Wound botulism MalaCards C0812426 Kidney problem C0520575 Acute pyelonephritis UMLS C0007758 Cerebellar ataxia C1366535 Avp gene HSDN C4084726 Distress cough C0950123 Inborn genetic disease HSDN C0035232 Diaphragmatic paralysis C1839259 Bulbo-spinal atrophy, x-linked HSDN C0241210 Speaking delay C1857355 Leigh syndrome , french canadian type HPO C0009806 Constipate C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0019621 Histiocytosis, langerhans-cell HSDN C0036572 Convulsion C1835819 Pituitary anomalies with holoprosencephaly-like features (disorder) HPO|UMLS C1963281 Vomiting adverse event C0398623 Thrombophilia HSDN C0000727 Abdomen acute C0023290 Leishmaniasis, visceral HSDN C3815497 Cough C0037354 Smallpox HSDN C4084766 Vomiting C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0038506 Stutter C0677614 Encounter due to convalescence HSDN C0005745 Blepharoptosis C4015167 Mental retardation, autosomal dominant 30 MalaCards C1384666 Decreased hearing C3554159 Deafness, autosomal recessive 84b MalaCards C4085211 Pain distress question C0029423 Cartilaginous exostosis HSDN C0042571 Vertigo subjective C0032209 Platybasia HSDN C4084726 Distress cough C0003811 Cardiac arrhythmia HSDN C0162298 Stiffness joints C0410189 Muscular dystrophy, emery-dreifuss OrphaNet|MalaCards C0151686 Growth retardation C1955934 Trichothiodystrophy syndromes MalaCards C0242936 Center pain C0032227 Pleural effusion disorder HSDN C0034933 Abnormal reflexes C0004153 Atherosclerosis HSDN C4084726 Distress cough C1619738 Immune reconstitution inflammatory syndrome HSDN C0020578 Hyperventilate C0007789 Cerebral palsy HSDN C0241157 Skin pustule C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C4085549 Dizziness C0023267 Fibroid tumor HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043255 Stab wound HSDN C0043094 Weight gain C0038579 Substance abuse, intravenous HSDN C0020505 Excessive eating C0024919 Behavior, maternal HSDN C0023014 Developmental disorder language C0024748 Alpha-mannosidosis HSDN C0018777 Deafness, conductive C0432292 Familial expansile osteolysis HPO C0018681 Headache, cephalalgia C0039984 Thoracic outlet syndrome HSDN C0085593 Chill C1962962 Hyperpigmentation adverse event HSDN C1963091 Diarrhea adverse event C0007932 Chagas' disease + no organ inv DiseaseOntology|MalaCards C1971624 Appetite absent C3273116 Gallbladder net MalaCards C0018834 Brash C0011581 Depressive disorder HSDN C0004941 Behavioral symptoms C0796081 Growth mental deficiency syndrome of myhre MalaCards C0027497 Queasy C0004096 Asthma HSDN C0426579 Anorexia symptom C0221036 Acrodermatitis enteropathica HPO C0344315 Mood depressed C3494506 Pseudohypoparathyroidism, type ia HPO C2984058 Have pain C0019522 Adenoma, sweat gland HSDN C0018681 Headache, cephalalgia C1858592 Carney triad MalaCards C0000737 Abdomen pain C1546847 Entity name part type - family HSDN C0015230 Exanthem C0263324 Erythema neonatorum UMLS C0162298 Stiffness joints C1859405 Bowen-conradi syndrome OrphaNet|HPO|MalaCards C0040259 Tinea pedis C0011603 Dermatitis HSDN C3146279 Coma C0033873 Psychiatry HSDN C0028738 Nystagmus C2931391 Cataract mental retardation anal atresia urinary defects OrphaNet|MalaCards C0025222 Black stool C1335686 Neuroendocrine neoplasm of rectum MalaCards C2984057 Have nausea C2937287 Hematolysis HSDN C0020649 Blood pressure decreased C2242987 Benign mastocytoma MalaCards C0393588 Dystonias paroxysmal C1970238 Episodic kinesigenic dyskinesia 2 MalaCards|UMLS C0424853 Finger mass C0409781 Villonodular synovitis of distal interphalangeal joint of finger UMLS C0018784 Deafness sensorineural C0006118 Brain neoplasms HSDN C0013404 Respiratory difficulty C0155883 Chronic obstructive asthma MalaCards C0015672 Decreased energy C0023364 Leptospirosis HSDN C0012833 Dizzy C0006277 Bronchitis HSDN C0575081 Abnormal gait C0017083 Gangliosidoses MalaCards C0085688 Engorgement breast C0157645 Engorgement of breasts associated with childbirth, delivered, with mention of postpartum complication UMLS C0575081 Abnormal gait C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C3665492 Pigmentations C0004779 Basal cell nevus syndrome MalaCards C2984057 Have nausea C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0019572 Hairiness C0030584 Parovarian cyst HSDN C3887784 Decreased urine output C0040524 Septic toxemia HSDN C0004941 Behavioral symptoms C3149276 Chromosome 16p12.1 deletion syndrome, 520-kb HPO C1000483 Genus anemia C2931646 Oculocerebral hypopigmentation syndrome type preus MalaCards C1971624 Appetite absent C0021280 Infant nutrition disorder HSDN C0031911 Pigment deposition C0152013 Adenocarcinoma of lung (disorder) MalaCards C0013404 Respiratory difficulty C1292753 Primary effusion lymphoma OrphaNet|HSDN|MalaCards C1963281 Vomiting adverse event C3812171 Bradycardia by ecg finding HSDN C0003079 Pupillary inequality C0010267 Cranial nerve neoplasms HSDN C2919142 Short stature adverse event C0796094 Blepharophimosis syndrome ohdo type MalaCards C0020672 Body temperature decreased C0032019 Pituitary neoplasms HSDN C0150055 Pain chronic C0009241 Cognition disorders HSDN C1963249 Tinnitus adverse event C0017638 Glioma HSDN C3887873 Hearing loss C0009324 Ulcerative colitis HSDN C0221263 Cafe au lait spot C3698541 Ohdo syndrome, maat-kievit-brunner type MalaCards C0035232 Diaphragmatic paralysis C0236969 Substance-related disorders HSDN C2126169 Sore on right side of mouth C0149745 Oral ulcer UMLS C0018772 Deafness C0259779 Fibrous dysplasia HSDN C0700072 Encounter due to stillbirth C0025237 Melnick-needles syndrome HPO C1963137 Hydrocephalus adverse event C3266101 22q11 partial monosomy syndrome HPO C0149840 Senile tremor C2026458 Cerebral degenerations, extrapyramidal and movement disorders UMLS C0497406 Over weight C0004161 Athletic injuries HSDN C4085211 Pain distress question C0242996 Learning, maze HSDN C0017181 Gastrointestinal bleed C1861194 Thrombasthenia-thrombocytopenia, hereditary MalaCards|HPO C1963237 Insomnia adverse event C0085209 Bovine spongiform encephalitis MalaCards C3829611 Nausea frequency C0022408 Arthropathy HSDN C1962972 Proteinuria adverse event C0002989 Epithelioid hemangioma of skin HSDN C0036659 Sensation disorder C0021368 Inflammation HSDN C1527344 Dysphonia C0040583 Tracheal stenosis HSDN C0349588 Stature short C1850040 Pelviscapular dysplasia OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0012561 Broad tapeworm infection DiseaseOntology|HSDN C0151908 Dry skin C0001529 Dercum disease MalaCards C4084725 Usual severity cough C1527406 Rhizomelic pseudopolyarthritis MalaCards C0000737 Abdomen pain C0001807 Aggressive behavior HSDN C2015928 Outcomes otolaryngology ear pain C1853554 Radiation induced meningioma MalaCards C0007758 Cerebellar ataxia C1843920 Coenzyme q10 deficiency HPO C0020438 Hypercalciuria C0036202 Sarcoidosis MalaCards|HSDN|HPO C4084725 Usual severity cough C1527298 Dysentery, bacillary HSDN C4085549 Dizziness C0027531 Neck injury HSDN C0012833 Dizzy C0024904 Mastoiditis HSDN C0020673 Hypothermia (central) (local) C0007570 Celiac disease HSDN C0020672 Body temperature decreased C2931542 Shapiro syndrome OrphaNet|MalaCards C4085317 Diarrhea frequency C1510428 Cerebral abscess HSDN C0026821 Cramp C0027055 Myocardial reperfusion injury HSDN C0042928 Paralysis vocal cord C0011581 Depressive disorder HSDN C0036572 Convulsion C4014354 Pontocerebellar hypoplasia, type 9 MalaCards|UMLS C0018772 Deafness C0035412 Rhabdomyosarcoma HSDN C2919142 Short stature adverse event C2931247 Chromosome 17, trisomy 17q22 OrphaNet|MalaCards C4085210 Usual severity pain C0043255 Stab wound HSDN C0020672 Body temperature decreased C1547046 Kind of quantity - taste HSDN C0917816 Deficiency mental C1839320 Childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness MalaCards C0018524 Hallucinate C0282513 Primary progressive aphasia (disorder) HPO C2315100 Pediatric failure to thrive C0265241 Franceschetti-klein syndrome MalaCards|HPO C1963091 Diarrhea adverse event C1420653 Tcn2 gene HPO C0042256 Vaginal pruritus C0459146 Disorder of soft tissue of body cavity UMLS C0036572 Convulsion C0795832 9p tetrasomy MalaCards C0015468 Face pain C0019196 Hepatitis c HSDN C1963065 Apnea adverse event C1968556 Encephalopathy, neonatal severe, due to mecp2 mutations HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1456781 Benign melanocytic nevus HSDN C0018784 Deafness sensorineural C0032131 Plasmacytoma HSDN C0424810 Periorbital swelling C0025235 Melkersson-rosenthal syndrome OrphaNet|MalaCards C0036572 Convulsion C0008628 Chromosome deletion MalaCards|HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0016057 Fibrosarcoma HSDN C4084767 Bothered by vomiting C0042076 Urologic neoplasms HSDN C0233794 Memory impaired C2931859 Acquired cjd MalaCards C0020672 Body temperature decreased C0242488 Acute lung injury HSDN C0018772 Deafness C0008628 Chromosome deletion MalaCards|HSDN C1963093 Dizziness adverse event C0007786 Brain ischemia HSDN C0027498 Nausea vomiting C0030521 Parathyroid neoplasms MalaCards C2237041 Shox gene with short stature C1845285 Martin-probst deafness-mental retardation syndrome OrphaNet|MalaCards C0030552 Paralysis partial C0282207 Cronkhite-canada syndrome MalaCards C4084776 Weight loss C1866552 Paragangliomas 2 (disorder) MalaCards C4084725 Usual severity cough C1849554 Lymphangiectasia, pulmonary, congenital OrphaNet|MalaCards C1962976 Ventricular fibrillation adverse event C1838527 Long qt syndrome 3, acquired, susceptibility to HPO C0476273 Distress respiratory C3553607 Mitochondrial pyruvate carrier deficiency MalaCards C2096293 Ent surgical result ear vertigo C0033845 Pseudotumor cerebri HSDN C0037316 Not enough sleeping C0270857 Epilepsy, reflex HSDN C0233763 Hallucinations visual C4013648 Polymicrogyria, bilateral temporooccipital MalaCards|UMLS C0000737 Abdomen pain C0042830 Perception visual HSDN C0026838 Spasticity muscle C3150315 Aicardi-goutieres syndrome 1, autosomal dominant HPO C0234146 Absent reflex C0265221 Walker-warburg congenital muscular dystrophy MalaCards C0003862 Pain joint C0023418 Leukemia HSDN C4084769 Vomiting frequency C0027022 Myeloproliferative disease HSDN C1963184 Nystagmus adverse event C3554321 Basal ganglia calcification, idiopathic, 4 MalaCards C2919142 Short stature adverse event C1304205 Neutrophilic urticaria MalaCards C0034933 Abnormal reflexes C0016989 Galvanic skin response HSDN C0018991 Paralysis one side of body C0029443 Osteomyelitis HSDN C0242936 Center pain C0152427 Polydactyly HSDN C3641756 Have diarrhea C0524620 Metabolic syndrome x HSDN C2315100 Pediatric failure to thrive C3151867 Chtd1 MalaCards|HPO C0751495 Seizure focal C1853554 Radiation induced meningioma MalaCards C0518090 Frequency of pain question C0037199 Sinusitis HSDN C0007758 Cerebellar ataxia C1847640 Kufor-rakeb syndrome MalaCards C4084802 Usual severity diarrhea C0836924 Thrombocytosis HSDN C2919142 Short stature adverse event C3887992 Thyrotropin-releasing hormone deficiency MalaCards C0007758 Cerebellar ataxia C1861736 Spinocerebellar ataxia 31 (disorder) HPO C2919142 Short stature adverse event C3554594 Steel syndrome MalaCards C4084725 Usual severity cough C2239176 Liver carcinoma HSDN C0020673 Hypothermia (central) (local) C0008058 Chilblains HSDN C0242936 Center pain C0041755 Adverse reaction to drug HSDN C0427068 Legs weakness C3888208 Spastic paraplegia 41, autosomal dominant MalaCards C0042571 Vertigo subjective C0040034 Thrombocytopenia HSDN C1963180 Neck pain adverse event C0003838 Arterial occlusive diseases HSDN C0027497 Queasy C0030568 Parkinsonism, postencephalitic HSDN C4084766 Vomiting C0026769 Multiple sclerosis HSDN C0851578 Disorder sleep C0243026 Sepsis HSDN C0423693 Child growing pains C2015802 Other orthopedic disorders UMLS C0043094 Weight gain C0206603 Circoviridae infection HSDN C0034150 Skin purpura C0020981 Angioimmunoblastic lymphadenopathy HSDN C0037763 Spasm C0039841 Thiamine deficiency HSDN C0018991 Paralysis one side of body C0338488 Alternating hemiplegia of childhood UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0014536 Epidural tumor HSDN C0003079 Pupillary inequality C0019114 Hemosiderosis HSDN C4084723 Constipation C0023176 Lead poisoning MalaCards|HSDN C1549543 Administration method - pain C2911243 Encounter due to family history of colonic polyps HSDN C0150055 Pain chronic C0162429 Malnutrition UMLS C0023530 Leukopenia C0221023 Cyclic neutropenia OrphaNet|HPO C0030552 Paralysis partial C0406810 Carney complex HSDN C0010200 Cough symptom C0042487 Venous thrombosis HSDN C0547030 Sensory perceptual alteration: visual C0431128 Papillary craniopharyngioma UMLS C0018772 Deafness C0796059 Oculopalatoskeletal syndrome MalaCards C0521532 Diaphragmatic weakness C0340427 Familial dilated cardiomyopathy MalaCards C4084768 Usual severity vomiting C0001973 Alcoholic intoxication, chronic HSDN C1069915 Vertigo C0020502 Hyperparathyroidism HSDN C0011991 Loose stools C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C1145670 Failure respiratory C0035372 Rett syndrome OrphaNet|HPO|MalaCards C0003113 Anomia C0007781 Intracranial embolism and thrombosis HSDN C0002962 Angina C0005940 Bone diseases HSDN C0231218 Malaise generalized C1519184 Intrahepatic cholangiocarcinoma with extensive sarcomatous changes UMLS C0017181 Gastrointestinal bleed C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C4085211 Pain distress question C4041080 Neurocognitive disorders HSDN C3463815 Feel fatigue C0018567 Hand dermatoses HSDN C3494358 Characteristic, prodromal C0025235 Melkersson-rosenthal syndrome HSDN C2237041 Shox gene with short stature C0796038 Mcdonough syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0085426 Gram-positive bacterial infections HSDN C3544135 Genital paraesthesia C1142014 Paraesthesia of genital female UMLS C4085210 Usual severity pain C0019326 Ventral hernia HSDN C0542476 Forgetful C0220669 Familial benign neonatal epilepsy MalaCards|HPO C0026884 Muteness C1853578 Neuroferritinopathy MalaCards|HPO C1963091 Diarrhea adverse event C1962958 Hematoma adverse event HSDN C0398650 Idiopathic thrombocytopenia purpura C0011854 Diabetes mellitus, insulin-dependent HSDN C0042420 Vasovagal episode C0033578 Prostatic neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0311375 Arsenic poisoning HSDN C4084727 Cough frequency C0009375 Colonic neoplasms HSDN C0022660 Acute kidney failure C1849386 Myoglobinuria, acute recurrent, autosomal recessive MalaCards|HPO C0750937 Appendicular ataxia C3280226 Spinocerebellar ataxia, autosomal recessive 11 MalaCards C0036572 Convulsion C1291463 Deficiency of phosphoserine phosphatase MalaCards|HPO|UMLS C0018777 Deafness, conductive C1138434 Disease, x-linked genetic HSDN C1963281 Vomiting adverse event C0010399 Crying HSDN C0043094 Weight gain C2219717 Menstrual periods stopped for over 6 months HSDN C0150055 Pain chronic C0011581 Depressive disorder HSDN C0013608 Cardiac edema C0018800 Cardiomegaly HSDN C0522224 Palsied C0038981 Swayback HSDN C0030486 Extremity paralysis, lower C0497327 Dementia HSDN C0011991 Loose stools C0035412 Rhabdomyosarcoma HSDN C4084775 Usual severity weight loss C2936350 Plaque, atherosclerotic HSDN C1557397 Adverse event associated with pain C0040765 Transsexualism HSDN C4085210 Usual severity pain C0020557 Hypertriglyceridemia HSDN C0349588 Stature short C1861196 Thoracopelvic dysostosis MalaCards C0234512 Prosopagnosia C0004352 Autistic disorder HSDN C3887638 Failure to thrive in infant C0014356 Enterocolitis MalaCards|HSDN C0557874 Global developmental delay C3889474 Bardet-biedl syndrome 16 MalaCards C0518090 Frequency of pain question C0034194 Pyloric stenosis HSDN C0917816 Deficiency mental C2931323 Heart-hand syndrome 2 MalaCards C0019825 Voice hoarseness C0242287 Isaacs syndrome HSDN C0030193 Sense of pain C0009353 Colles' fracture HSDN C0577567 Mass of urogenital structure C0042995 Vulvar neoplasms UMLS C0557874 Global developmental delay C3714980 Bardet-biedl syndrome 17 MalaCards C1963087 Constipation adverse event C0005586 Bipolar disorder HSDN C0019825 Voice hoarseness C0271585 Isolated trh deficiency MalaCards C0028738 Nystagmus C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C1549543 Administration method - pain C0029463 Osteosarcoma OrphaNet|HSDN|HPO C2984057 Have nausea C0041318 Tuberculosis, meningeal HSDN C4084774 Have weight loss C0026755 Multiple carboxylase deficiency OrphaNet|MalaCards C4085549 Dizziness C0517555 Venous thrombosis after immobility HSDN C0010200 Cough symptom C2930674 Babesioses, human MalaCards C0085631 Abnormal excitement C0006147 Breast fed HSDN C3829611 Nausea frequency C0035229 Respiratory insufficiency HSDN C0027796 Neuralgias C0011854 Diabetes mellitus, insulin-dependent HSDN C0004604 Pain back C0004936 Mental disorders HSDN C3539893 Pelvic pain occurs with intercourse C0282606 Myomatous neoplasm HSDN C2984058 Have pain C0035923 German measles vaccine HSDN C0036396 Sciatica C1962979 Burn adverse event HSDN C2919142 Short stature adverse event C1836673 Branchiogenic-deafness syndrome OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013289 Duodenal diseases HSDN C1963281 Vomiting adverse event C0042164 Uveitis HSDN C4084774 Have weight loss C0029001 Onchocerciasis HSDN C2700617 Irritation - emotion C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C0557874 Global developmental delay C0796113 Nephroblastomatosis, fetal ascites, macrosomia and wilms tumor MalaCards|HPO C3463815 Feel fatigue C1841972 Glucocorticoid receptor deficiency OrphaNet|HPO C4084766 Vomiting C3163620 Hypotension adverse event HSDN C0015230 Exanthem C0276181 Flat-type smallpox UMLS C2015928 Outcomes otolaryngology ear pain C1336537 Supratentorial meningioma MalaCards C4085211 Pain distress question C0028064 Niemann-pick diseases HSDN C0042940 Disorder of voice C0007137 Squamous cell carcinoma HSDN C1963170 Hypothermia adverse event C0085183 Neoplasms, second primary HSDN C0016199 Pain flank C0030793 Pelvis tumor HSDN C2911647 Weight gain adverse event C0010356 Cross infection HSDN C0013362 Dysarthrias C3280226 Spinocerebellar ataxia, autosomal recessive 11 MalaCards C4085549 Dizziness C0024904 Mastoiditis HSDN C0030200 Intractable pain C0007786 Brain ischemia HSDN C1963071 Back pain adverse event C3814778 Hemolytic index HSDN C0576456 Poor feeding C1970253 Phosphoserine aminotransferase deficiency MalaCards C4085317 Diarrhea frequency C0029001 Onchocerciasis HSDN C1519353 Skin eruption papular C1866398 Proteus-like syndrome (disorder) MalaCards C1971624 Appetite absent C2586211 Thrombosis of blood vessel HSDN C0013362 Dysarthrias C0853240 Mobius ii syndrome MalaCards C0010038 Corneal opacity disorder C0268226 Type i mucolipidosis OrphaNet|HPO C0020578 Hyperventilate C0013926 Aeroembolism HSDN C0005745 Blepharoptosis C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C3203358 Alveolar hypoventilation C0033845 Pseudotumor cerebri HSDN C2919142 Short stature adverse event C2749685 Cystinosis, atypical nephropathic (disorder) HPO C3898969 Have been vomiting C1845862 Creatine deficiency, x-linked MalaCards|HPO C0006370 Bulimia C0020524 Disorders of excessive somnolence HSDN C0028738 Nystagmus C0549567 Pigmentation disorders MalaCards C0018681 Headache, cephalalgia C3495422 Finding relating to sexuality and sexual activity HSDN C0038002 Spleen enlargement C3888244 Aicardi-goutieres syndrome 7 MalaCards C0028738 Nystagmus C1862261 Bpes, type ii HPO C0036572 Convulsion C2930900 Beta-sarcoglycanopathy MalaCards C2919142 Short stature adverse event C2676231 Skeletal defects, genital hypoplasia, and mental retardation HPO C0917816 Deficiency mental C2745996 Fitzsimmons syndrome OrphaNet|MalaCards C0030193 Sense of pain C1546602 Specimen source codes - diverticulum HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0024081 Angina, ludwig HSDN C1963252 Tremor adverse event C0036868 Sex chromosome aberrations HSDN C1549543 Administration method - pain C0950123 Inborn genetic disease HSDN C0013421 Dystonia C0007137 Squamous cell carcinoma HSDN C0424755 Fever symptoms C0030920 Peptic ulcer HSDN C4049602 Hyperactivity C1848488 Pierre robin syndrome with fetal chondrodysplasia OrphaNet C4085210 Usual severity pain C0085270 Orbit pseudotumor HSDN C4084802 Usual severity diarrhea C0020564 Hypertrophy HSDN C0022346 Yellow skin C0024141 Lupus erythematosus, systemic HSDN C0042963 Symptoms vomiting C0038536 Subcutaneous emphysema HSDN C0000737 Abdomen pain C1335183 Ovarian surface papilloma UMLS C0002962 Angina C0011884 Diabetic retinopathy HSDN C1963281 Vomiting adverse event C0001807 Aggressive behavior HSDN C0398650 Idiopathic thrombocytopenia purpura C0023892 Biliary cirrhosis HSDN C0034933 Abnormal reflexes C0011265 Presenile dementia HSDN C0018784 Deafness sensorineural C2937225 Biotin deficiency disease MalaCards C0013421 Dystonia C1855033 Mitochondrial myopathy with lactic acidosis MalaCards|HPO C0015300 Ocular proptosis C0040156 Thyrotoxicosis MalaCards C0263355 Scarlatiniform rash C0037274 Dermatologic disorders UMLS C0497247 Blood pressure elevation C2676191 Pituitary adenoma, familial isolated (disorder) HPO C1963093 Dizziness adverse event C0003125 Anorexia nervosa HSDN C0004604 Pain back C1556682 Adverse event associated with infection HSDN C1963180 Neck pain adverse event C0085094 Head injury closed HSDN C0026838 Spasticity muscle C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards C2984058 Have pain C0036093 Salivary gland diseases HSDN C2984058 Have pain C0005716 Blastomycosis HSDN C2984058 Have pain C0019372 Herpesviridae infections HSDN C0033774 Skin pruritus C1852297 Darier disease, segmental HPO C2029884 Hearing loss by exam C1857663 Yunis varon syndrome MalaCards C1557397 Adverse event associated with pain C1334928 Necrotic changes (finding) HSDN C0013395 Indigestion C0349530 Early gastric cancer UMLS C1279888 Proteinuria of undiagnosed cause C0039981 Thoracic neoplasms HSDN C0022346 Yellow skin C0243026 Sepsis HSDN C0036572 Convulsion C3280970 Porencephaly 2 MalaCards|UMLS C1549543 Administration method - pain C1704421 Skin pigmentation disorder HSDN C1963091 Diarrhea adverse event C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0030552 Paralysis partial C2930812 Generalized elastolysis MalaCards C0015230 Exanthem C0153062 Viral exanthem UMLS C1384666 Decreased hearing C0795822 8 rec syndrome OrphaNet|MalaCards C0019209 Large liver C0751161 Udpglucose 4-epimerase deficiency disease OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0520799 Acute radiation syndrome HSDN C0036572 Convulsion C1864651 Gaucher disease, atypical, due to saposin c deficiency HPO C0002170 Alopecia disorders C1303073 Nicolaides baraitser syndrome MalaCards C0020673 Hypothermia (central) (local) C0042018 Urinary calculi HSDN C0042963 Symptoms vomiting C0023518 Leukocytosis UMLS C0000737 Abdomen pain C1333761 Gastric adenosquamous carcinoma UMLS C0413252 Hypothermia due to exposure C1962983 Cataract adverse event HSDN C0017565 Gingiva hemorrhage C0043194 Wiskott-aldrich syndrome MalaCards|HPO C4084775 Usual severity weight loss C0270611 Brain damage HSDN C0024031 Back pain lower back C0023473 Myeloid leukemia, chronic HSDN C4085548 Usual severity dizziness C2609414 Acute kidney injury HSDN C0231341 Aging premature C0042900 Vitiligo HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3489393 Hiatal hernia HSDN C0575081 Abnormal gait C0205713 Roussy-levy syndrome (disorder) OrphaNet|HPO C0015469 Facial paralysis C0812393 Cancer patients and suicide and depression HSDN C0007758 Cerebellar ataxia C0011269 Dementia, vascular HSDN C2984058 Have pain C0032226 Pleural diseases HSDN C0037316 Not enough sleeping C2698559 Breakfast HSDN C2029884 Hearing loss by exam C0021368 Inflammation HSDN C1000483 Genus anemia C0268131 Omp decarboxylase deficiency MalaCards C4084768 Usual severity vomiting C0033873 Psychiatry HSDN C0015672 Decreased energy C1881674 Medical device emits smoke HSDN C2984057 Have nausea C0027873 Neuromyelitis optica MalaCards|HSDN C0011991 Loose stools C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C0019079 Bloody sputum C0011581 Depressive disorder HSDN C0042963 Symptoms vomiting C0042812 Acuity visual HSDN C0085593 Chill C0085082 Fungemia HSDN C0012833 Dizzy C0456892 Csf low pressure HSDN C0018772 Deafness C0043251 Wounds and injuries HSDN C0424755 Fever symptoms C0037933 Spinal diseases HSDN C0030552 Paralysis partial C0031154 Peritonitis HSDN C0040034 Thrombocytopenia C1847827 Lig4 syndrome MalaCards C0851578 Disorder sleep C0518449 Control of hip fracture risk HSDN C0019209 Large liver C0281508 Desmoplastic small round cell tumor OrphaNet|HPO|MalaCards C0010200 Cough symptom C0005695 Bladder neoplasm HSDN C0042963 Symptoms vomiting C0020522 Delayed hypersensitivity HSDN C0018772 Deafness C0018213 Graves disease HSDN C4084726 Distress cough C0011644 Scleroderma OrphaNet|MalaCards C0242936 Center pain C1879338 Bereavement, life event HSDN C3539896 Pelvic pain occurs with urination C1552262 Nurse practitioner - family HSDN C0026858 Musculoskeletal pain C0206752 Alphavirus infections HSDN C1963086 Confusion adverse event C0002063 Alkalosis HSDN C0150055 Pain chronic C0520719 Spinopontine atrophy MalaCards C0012766 Skin sensation disturbance C0152027 Sensory disorders UMLS C0424755 Fever symptoms C0007138 Carcinoma, transitional cell HSDN C0021359 Infertility C0342442 Acth-dependent cushing's syndrome OrphaNet C0038990 Sweats C0001080 Achondroplasia OrphaNet|HPO|MalaCards C0015970 Fever unknown origin C0023895 Liver diseases HSDN C2315100 Pediatric failure to thrive C3281234 Combined oxidative phosphorylation deficiency 9 MalaCards C0030193 Sense of pain C0020626 Hypoparathyroidism HSDN C0037771 Paraparesis spastic C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO|UMLS C1263846 Attention deficit disorder with hyperactivity C2720163 Placental steroid sulfatase deficiency OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C0023380 Lethargy C0751955 Brain infarction HSDN C0027497 Queasy C2981150 Uranostaphyloschisis HSDN C4084774 Have weight loss C0162624 Enoplida infection HSDN C0003862 Pain joint C0268202 Beta-sitosterolemia MalaCards C4084788 Have dizziness C0017612 Glaucoma, open-angle HSDN C4084769 Vomiting frequency C0022107 Irritable mood HSDN C0020438 Hypercalciuria C0032371 Poliomyelitis HSDN C0587047 Mass of trunk C0236048 Polyposis, gastric UMLS C4085862 Bothered by nausea C0010340 Critical illness HSDN C0018932 Bright red rectal bleeding C0017150 Gastrinoma MalaCards C2132198 Abnormal blistering of the skin C1851573 Transient bullous dermolysis of the newborn OrphaNet|HPO C1963071 Back pain adverse event C0009946 Conversion disorder HSDN C4084774 Have weight loss C0243026 Sepsis HSDN C0577567 Mass of urogenital structure C0269188 Uterine cyst UMLS C0042384 Vasculitis, nonspecific C0039263 Takayasu arteritis OrphaNet|HPO|MalaCards C2039130 Bottom of tongue swollen C0236068 Tongue swelling UMLS C0030486 Extremity paralysis, lower C0037116 Silicosis HSDN C1527344 Dysphonia C2239136 Laryngocele HSDN C0012569 Double vision C0001163 Vestibulocochlear nerve diseases HSDN C0522224 Palsied C0019555 Hip dislocation, congenital HSDN C0013421 Dystonia C0042514 Tachycardia, ventricular HSDN C3641756 Have diarrhea C0032131 Plasmacytoma HSDN C0005745 Blepharoptosis C0010273 Craniofacial dysostosis MalaCards C0018681 Headache, cephalalgia C0086957 Naffziger syndrome HSDN C3815497 Cough C0010356 Cross infection HSDN C0235053 Pricking skin sensation C0030554 Paresthesia UMLS C3665347 Vision impaired C1867300 Retinitis pigmentosa 9 MalaCards C1961131 Cough adverse event C0022660 Kidney failure, acute HSDN C2024878 Cardiovascular surgery result: dyspnea C3280574 Surfactant metabolism dysfunction, pulmonary, 5 MalaCards C1549543 Administration method - pain C0019270 Hernia HSDN C0857305 Thrombocytopenia purpura C0036220 Kaposi sarcoma HSDN C0036572 Convulsion C2020541 Strabismus HSDN C0039231 Heartbeats increased C1865018 Short qt syndrome 3 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0001621 Adrenal gland diseases HSDN C0035229 Respiratory function impaired C1721007 Pachyonychia congenita, type 2 (disorder) MalaCards C0460137 Push down or depress C2931859 Acquired cjd MalaCards C0022660 Acute kidney failure C1720821 Membranoproliferative glomerulonephritis, type iii MalaCards C0878773 Bladder hyperactive C1962986 Glaucoma adverse event HSDN C0002962 Angina C0023798 Lipoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0039483 Giant cell arteritis HSDN C1963086 Confusion adverse event C0041327 Tuberculosis, pulmonary HSDN C0009421 Comatose C0020473 Hyperlipidemia HSDN C0086565 Liver function abnormal C2698658 Orofaciodigital syndrome type 1 MalaCards C0333262 Vesicles C1857449 Cutaneous photosensitivity and colitis, lethal MalaCards C1963077 Bone pain adverse event C0029454 Osteopetrosis OrphaNet|MalaCards C0036572 Convulsion C0027149 Myxoma HSDN C0522179 Anxiety death C0150063 Feeling powerless UMLS C2362324 Pediatric obesity C0001614 Adrenal cortex diseases HSDN C0020578 Hyperventilate C0086543 Cataract nos HSDN C0917816 Deficiency mental C2675336 Duplication 15q11-q13 syndrome OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0003490 Aortic arch syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C1838163 Osler-rendu-weber syndrome 2 MalaCards|HPO C0013404 Respiratory difficulty C0221759 Brachial plexus neuritis HSDN C1963093 Dizziness adverse event C0162526 Aids-related opportunistic infections HSDN C4085211 Pain distress question C2607914 Allergic rhinitis (disorder) HSDN C0018834 Brash C0428953 Ecg infarction myocardial HSDN C0033377 Caudal displacement C0751552 Malignant neoplasm of thymus MalaCards C0557874 Global developmental delay C3539013 Aicardi-goutieres syndrome 6 MalaCards C0398650 Idiopathic thrombocytopenia purpura C0796004 Kabuki make-up syndrome MalaCards|HPO C0751495 Seizure focal C0278202 Seizure, partial, illusions, hallucinations UMLS C0018926 Emesis bloody C0023269 Leiomyosarcoma HSDN C0034933 Abnormal reflexes C0033941 Psychoses, substance-induced HSDN C4085661 Usual severity nausea C1881674 Medical device emits smoke HSDN C0020455 Hypergammaglobulinemia C0035369 Retroviridae infections HSDN C0033774 Skin pruritus C1275968 Senile asteatotic eczema UMLS C0007815 Cerebrospinal fluid rhinorrhoea C0024958 Maxillary sinus neoplasms HSDN C0006370 Bulimia C0016658 Fracture bone HSDN C3641755 Have constipation C1527336 Sjogren's syndrome HSDN C0742308 Chest pain site right_lower_thorax C0741025 Chest problem UMLS C4085211 Pain distress question C0206743 Rhabdoid tumor HSDN C0018772 Deafness C1138434 Disease, x-linked genetic HSDN C0042963 Symptoms vomiting C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0012569 Double vision C2936781 Generalized myotonia of thomsen HSDN C1963184 Nystagmus adverse event C3888081 L-2-hydroxyglutaric acidemia MalaCards C0340288 Angina stable C0004153 Atherosclerosis HSDN C0043094 Weight gain C3495422 Finding relating to sexuality and sexual activity HSDN C0398650 Idiopathic thrombocytopenia purpura C0041296 Tuberculosis HSDN C0030554 Abnormal sensation C0027663 Neoplasms, multiple primary HSDN C0004604 Pain back C1258104 Diffuse scleroderma HSDN C0013595 Eczematous dermatitis C1863204 Adult syndrome MalaCards|HPO C1549543 Administration method - pain C0030790 Pelvis infection HSDN C0454644 Delayed language development C1845902 Fg syndrome 2 MalaCards|HPO C0010520 Skin cyanosis C0021361 Female infertility HSDN C1549543 Administration method - pain C0007781 Intracranial embolism and thrombosis HSDN C2364111 Gustatory anesthesia C2827407 Infectious otitis media HSDN C0600142 Flash hot C1963138 Hypertension adverse event HSDN C3203358 Alveolar hypoventilation C1548578 Location characteristic id - smoking HSDN C0012569 Double vision C0011854 Diabetes mellitus, insulin-dependent HSDN C0027497 Queasy C0042961 Intestinal volvulus HSDN C0013604 Edematous C0026946 Mycoses HSDN C0032617 High urine output C0032001 Pituitary apoplexy HSDN C3539891 Pelvic pain to the rear C0563150 Catastrophization HSDN C1963091 Diarrhea adverse event C1532560 Plasmacytoma - category HSDN C1963252 Tremor adverse event C1457883 Aggressive reaction HSDN C0030794 Pelvis pain C0206630 Endometrial stromal sarcoma HSDN C0231341 Aging premature C0424688 Small head HSDN C0857305 Thrombocytopenia purpura C0029408 Degenerative polyarthritis HSDN C0454644 Delayed language development C0796249 Mental retardation, x linked 47 HPO C0012833 Dizzy C0271487 Vertiginous disorder UMLS C0151786 Weakness muscle C0035923 German measles vaccine HSDN C0085642 Asphyxia reticularis C0036202 Sarcoidosis HSDN C3641755 Have constipation C2931518 Plexosarcoma MalaCards C0917816 Deficiency mental C1865349 Ethylmalonic encephalopathy HPO C0033774 Skin pruritus C1963139 Hypopigmentation adverse event HSDN C0036572 Convulsion C0002453 Amenorrhea HSDN C0349588 Stature short C2700425 Ehlers-danlos syndrome, dermatosparaxis type HPO C0018681 Headache, cephalalgia C0041228 African trypanosomiasis DiseaseOntology C0030552 Paralysis partial C0004275 Attitude health HSDN C0850149 Cough dry C1535939 Pneumocystis jiroveci pneumonia DiseaseOntology|MalaCards C0234146 Absent reflex C4014648 Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 MalaCards C0033377 Caudal displacement C1857780 Joubert syndrome 5 MalaCards C4085211 Pain distress question C0024116 Lung diseases, fungal HSDN C3463815 Feel fatigue C0152998 Acute nonparalytic poliomyelitis, poliovirus, unspecified type DiseaseOntology|MalaCards C0013404 Respiratory difficulty C1263846 Attention deficit hyperactivity disorder HSDN C0242936 Center pain C0265706 Gastroschisis HSDN C1557397 Adverse event associated with pain C2021655 Transvaginal ultrasound: anencephaly of fetus HSDN C0013604 Edematous C0010692 Cystitis HSDN C0349588 Stature short C0268341 Ehlers-danlos syndrome type 5 OrphaNet|MalaCards C4050613 Anxiety C3683846 Chromosome 17p deletion syndrome MalaCards C0085602 Polydypsia C0268450 Gitelman syndrome MalaCards|HPO|UMLS C0242936 Center pain C0031154 Peritonitis HSDN C0917816 Deficiency mental C1846046 Spastic paraplegia 16, x-linked (disorder) MalaCards C4084725 Usual severity cough C3541994 Drug hypersensitivity syndrome MalaCards C4084774 Have weight loss C0032226 Pleural diseases HSDN C0030193 Sense of pain C0158266 Intervertebral disc degeneration HSDN C0014089 Functional encopresis C1552262 Nurse practitioner - family HSDN C2024878 Cardiovascular surgery result: dyspnea C0036421 Systemic scleroderma MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0263843 Band iliotibial syndromes HSDN C0037763 Spasm C0004096 Asthma HSDN|UMLS C0006370 Bulimia C0022661 Kidney failure, chronic HSDN C4085210 Usual severity pain C0026936 Mycoplasma infections HSDN C0162835 Hypopigmentation C1096902 Infantile sialic acid storage disease HPO C2911645 Weight loss adverse event C0410422 Chronic multifocal osteomyelitis OrphaNet|MalaCards C4085317 Diarrhea frequency C0031149 Peritoneal neoplasms HSDN C4084784 Diarrhea C0011854 Diabetes mellitus, insulin-dependent HSDN C0037036 Increased salivation C0796003 Juberg-marsidi syndrome HPO C0000727 Abdomen acute C0038454 Cerebrovascular accident HSDN C4084727 Cough frequency C0037120 Pneumonia, nitrogen dioxide HSDN C0004134 Dyssynergia C0029340 Orthomolecular therapy HSDN C0018772 Deafness C1962976 Ventricular fibrillation adverse event HSDN C1963071 Back pain adverse event C0025500 Mesothelioma HSDN C0032781 Postnasal drip C0035243 Respiratory tract infections UMLS C0004604 Pain back C1704275 Pyomyositis HSDN C0020578 Hyperventilate C0008625 Chromosome aberrations HSDN C2315100 Pediatric failure to thrive C1848410 Xeroderma pigmentosum, variant type MalaCards C0851578 Disorder sleep C0950124 Papillomavirus infections HSDN C4085211 Pain distress question C1548484 Rheumatic fever vaccine HSDN C0000737 Abdomen pain C0016751 Hereditary fructose intolerance syndrome HPO|UMLS C2919142 Short stature adverse event C0342642 Autosomal dominant hypophosphatemic rickets MalaCards|HPO C0557874 Global developmental delay C3151036 Chromosome 1p32-p31 deletion syndrome HPO C2919142 Short stature adverse event C1867443 Distinctive craniofacial features with pterygia and mental retardation OrphaNet|MalaCards C0344315 Mood depressed C2931082 Familial apoceruloplasmin deficiency MalaCards C3641756 Have diarrhea C0007798 Cerebral ventricle neoplasm HSDN C0242936 Center pain C0333641 Atrophic HSDN C0038506 Stutter C0020517 Hypersensitivity HSDN C0004604 Pain back C1334698 Meningothelial cell neoplasm MalaCards C0018681 Headache, cephalalgia C0035305 Retinal detachment HSDN C0011991 Loose stools C0006285 Bronchopneumonia HSDN C3539895 Pelvic pain occurs with bowel movement C0017416 Genital neoplasms, female HSDN C0027497 Queasy C1302282 Chromaffin cell neoplasm MalaCards C0030486 Extremity paralysis, lower C0009375 Colonic neoplasms HSDN C1069915 Vertigo C2674766 Myokymia 1 HPO C3812171 Bradycardia by ecg finding C3697638 Familial short qt syndrome MalaCards C0015469 Facial paralysis C0032584 Polyps HSDN C0152459 Striae C1546558 Specimen source codes - blister HSDN C0039870 Leanness C0852795 Increased insulin level HSDN C2203646 Jaundice C0848377 Trauma to the abdomen HSDN C0030552 Paralysis partial C0700327 Clinical findings relating to memory HSDN C0349588 Stature short C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C3815497 Cough C0007820 Cerebrovascular disorders HSDN C2096293 Ent surgical result ear vertigo C0020550 Hyperthyroidism HSDN C0424755 Fever symptoms C0043541 Zygomycoses HSDN C0013421 Dystonia C0018188 Granuloma HSDN C2984057 Have nausea C0034088 Pulmonary valve insufficiency HSDN C0034150 Skin purpura C0014527 Epidermolysis bullosa HSDN C0036572 Convulsion C0234974 Simple partial seizures UMLS C0015469 Facial paralysis C0027746 Nerve degeneration HSDN C4084775 Usual severity weight loss C0011630 Dermatomycoses HSDN C0242936 Center pain C0023443 Hairy cell leukemia HSDN C2242996 Tingling C0007820 Cerebrovascular disorders HSDN C0518090 Frequency of pain question C0024116 Lung diseases, fungal HSDN C1963252 Tremor adverse event C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0848203 Male pelvic pain C0033038 Ejaculatio praecox HSDN C0042514 Ventricular tachycardia C3151463 Cpvt3 MalaCards|HPO C0151786 Weakness muscle C0028768 Obsessive-compulsive disorder HSDN C4084769 Vomiting frequency C3146297 Study of behavior during childhood HSDN C1963065 Apnea adverse event C0544012 Aberfeld's syndrome MalaCards C4084775 Usual severity weight loss C0017412 Genital diseases, male HSDN C0030193 Sense of pain C0003490 Aortic arch syndrome HSDN C3541349 Syncope C0004352 Autistic disorder HSDN C0031911 Pigment deposition C0149782 Squamous cell carcinoma of lung MalaCards C2024878 Cardiovascular surgery result: dyspnea C0036095 Salivary gland neoplasms HSDN C4084725 Usual severity cough C0878544 Cardiomyopathies HSDN C2024893 Cardiovascular surgery result: fatigue C0035436 Rheumatic fever OrphaNet|HSDN|MalaCards C0015469 Facial paralysis C0019829 Hodgkin disease HSDN C0005745 Blepharoptosis C2931226 Thompson baraitser syndrome OrphaNet|MalaCards C0035229 Respiratory function impaired C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards C0030554 Abnormal sensation C0347555 Friction blister HSDN C0018784 Deafness sensorineural C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards|HPO C1963249 Tinnitus adverse event C0031118 Peripheral nervous system neoplasms HSDN C0850758 Pain pelvic C0520946 Emotional hypersensitivity HSDN C0424755 Fever symptoms C1868653 Pancreatitis, calcific HPO C0020538 Hbp C3887949 Apparent mineralocorticoid excess MalaCards C0241137 Skin pallor C0206733 Strawberry nevus of skin HSDN C4084767 Bothered by vomiting C0270639 Lateral sinus thrombosis HSDN C2315100 Pediatric failure to thrive C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C3813607 Infantile gastroesophageal reflux HSDN C0015230 Exanthem C0483368 Human anaplasmosis due to anaplasma phagocytophilum MalaCards C0231341 Aging premature C0005941 Bone diseases, developmental HSDN C2237041 Shox gene with short stature C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C1963281 Vomiting adverse event C0033845 Pseudotumor cerebri HSDN C1527344 Dysphonia C0205770 Choroid plexus papilloma HSDN C0848203 Male pelvic pain C0012746 Dissociative disorder HSDN C1963065 Apnea adverse event C0344315 Depressed mood HSDN C0237326 Defecation pain C2931876 Hirschsprung disease 1 MalaCards C2024878 Cardiovascular surgery result: dyspnea C1135191 Heart failure, systolic HSDN C0242936 Center pain C0022423 Judgement HSDN C0031911 Pigment deposition C1835398 Li-fraumeni syndrome 1 MalaCards C0009806 Constipate C1552262 Nurse practitioner - family HSDN C0013604 Edematous C2673642 Combined oxidative phosphorylation deficiency 5 MalaCards|HPO C4084774 Have weight loss C0018523 Hallervorden-spatz syndrome OrphaNet|MalaCards C0009763 Conjunctiva inflammation C0271270 Oculovestibuloauditory syndrome MalaCards C0013404 Respiratory difficulty C0038220 Status epilepticus HSDN C0878638 Tongue signs C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0019521 Hiccoughs C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C4084784 Diarrhea C0268386 Amyloid polyneuropathy, swiss type MalaCards C0917816 Deficiency mental C0796055 Mercaptolactate-cysteine disulfiduria OrphaNet|MalaCards C0349588 Stature short C0085132 Mucopolysaccharidosis vii HPO C4084784 Diarrhea C0018790 Cardiac arrest HSDN C1069915 Vertigo C1690964 Cataract HSDN C0030193 Sense of pain C0855010 Recurrent neuroepithelioma of bone UMLS C0848203 Male pelvic pain C0037397 Behavior social HSDN C0349588 Stature short C1300260 Spondylar and nasal alterations with striated metaphyses OrphaNet|MalaCards C2984057 Have nausea C0149931 Migraine disorders MalaCards C1962972 Proteinuria adverse event C0221204 Lytic lesion MalaCards C1963091 Diarrhea adverse event C0035637 Rinderpest HSDN C3506134 Cardiac defibrillator 'going off' C0340933 Icd malfunction UMLS C0017672 Pain tongue C0002871 Anemia HSDN C0024031 Back pain lower back C0002895 Anemia, sickle cell HSDN C4084802 Usual severity diarrhea C0025162 Megacolon toxic HSDN C0557874 Global developmental delay C4015447 Combined oxidative phosphorylation deficiency 23 MalaCards C4084766 Vomiting C1527348 Brain hypoxia HSDN C0018772 Deafness C0029182 Orbit (eye disorders) HSDN C0162834 Hyperpigmentation C1848410 Xeroderma pigmentosum, variant type OrphaNet|MalaCards C0011991 Loose stools C0008325 Cholecystitis HSDN C0018524 Hallucinate C0018802 Congestive heart failure HSDN C1963137 Hydrocephalus adverse event C0431289 Encephalocele, frontal OrphaNet|MalaCards C4085549 Dizziness C0029877 Ear inflammation HSDN C4085661 Usual severity nausea C0012147 Dientamoebiases DiseaseOntology C0234146 Absent reflex C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0002878 Anemia, hemolytic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0596263 Carcinogenesis HSDN C2315100 Pediatric failure to thrive C0342701 Transcobalamin ii deficiency MalaCards C2029884 Hearing loss by exam C0027765 Nervous system disorder HSDN C0151686 Growth retardation C0265329 Organoid nevus phakomatosis HPO C0030193 Sense of pain C0041408 Turner syndrome HSDN C4085211 Pain distress question C0085166 Bacterial vaginosis HSDN C0018784 Deafness sensorineural C3809875 Van maldergem syndrome 2 MalaCards C4084774 Have weight loss C0850803 Anaphylaxis (non medication) HSDN C0497406 Over weight C0015726 Focused anxiety HSDN C1549543 Administration method - pain C0023493 Adult t-cell lymphoma/leukemia HSDN C0917816 Deficiency mental C3150416 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 MalaCards|HPO C0026821 Cramp C0338503 Septo-optic dysplasia HSDN C4084766 Vomiting C0268322 Chester-type porphyria HPO C0013404 Respiratory difficulty C3814530 Skin vesicle HSDN C0030193 Sense of pain C0206696 Carcinoma, signet ring cell HSDN C3829611 Nausea frequency C1956418 Torsion abnormality HSDN C0039070 Collapse fleeting C0008073 Developmental disabilities HSDN C0751295 Memory loss or impairment C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy OrphaNet|HPO C0162835 Hypopigmentation C1857854 Proopiomelanocortin deficiency OrphaNet|HPO C0038002 Spleen enlargement C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C0026205 Pupillary constriction C1458155 Mammary neoplasms HSDN C0034933 Abnormal reflexes C0029456 Osteoporosis HSDN C0017672 Pain tongue C0011330 Dental calculus HSDN C0232466 Feeding difficulty C2931001 Congenital disorder of glycosylation type 1g MalaCards C2242996 Tingling C0008728 Churg-strauss syndrome HSDN C0162298 Stiffness joints C0432239 Kyphomelic dysplasia OrphaNet|MalaCards C1557397 Adverse event associated with pain C0027849 Neuroleptic malignant syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038536 Subcutaneous emphysema HSDN C0017181 Gastrointestinal bleed C2347126 Microscopic polyarteritis MalaCards C4049602 Hyperactivity C0268553 Hyperlysinemias HPO C0000737 Abdomen pain C0206632 Angiolipoma HSDN C1963093 Dizziness adverse event C0032962 Pregnancy complications HSDN C3887873 Hearing loss C3280296 Microcephaly-capillary malformation syndrome MalaCards C0028961 Urine output decreased C3541994 Drug hypersensitivity syndrome HSDN C0221752 Rbc urine C0002895 Anemia, sickle cell MalaCards|HPO C4084768 Usual severity vomiting C0031046 Pericarditis HSDN C0239574 Fever low grade C0004031 Aspergillosis, allergic bronchopulmonary OrphaNet|MalaCards C0522224 Palsied C1456781 Benign melanocytic nevus HSDN C4084784 Diarrhea C0006261 Bronchial diseases HSDN C0003862 Pain joint C0035613 Rift valley fever OrphaNet|MalaCards C0151889 Reflexes tendon increased C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0023012 Delay language C0410174 Fukuyama type congenital muscular dystrophy OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C3854315 Pseudoprimary hyperaldosteronism MalaCards C0003862 Pain joint C0043397 Yellow fever, jungle MalaCards C0424755 Fever symptoms C0023051 Laryngeal diseases HSDN C2700617 Irritation - emotion C1707400 Classic medulloblastoma MalaCards C0040264 Ear ringing sound C0030297 Pancreatic neoplasm HSDN C0042571 Vertigo subjective C0006818 Campylobacter infection HSDN C0520909 Ponv C0022758 Kap HSDN C0042755 Virilisation C0019693 Hiv infections HSDN C0018784 Deafness sensorineural C1858280 Charcot-marie-tooth neuropathy, type 4b2, with early-onset glaucoma HPO C0011175 Deficient fluid volume C0268621 Hepatic methionine adenosyltransferase deficiency MalaCards C4084724 Usual severity constipation C0007193 Cardiomyopathy, dilated HSDN C2911645 Weight loss adverse event C2609414 Acute kidney injury HSDN C0034155 Thrombotic thrombocytopenic purpura C1963084 Colitis adverse event HSDN C0557874 Global developmental delay C3809853 Mental retardation, autosomal recessive 39 MalaCards C1962972 Proteinuria adverse event C0012644 Animal disease models HSDN C1963087 Constipation adverse event C1962958 Hematoma adverse event HSDN C0013421 Dystonia C0220756 Niemann-pick disease, type c OrphaNet|HSDN|HPO|MalaCards C1260880 Nasal drip C0347095 Carcinoma in situ of nasal cavity, nos UMLS C0012833 Dizzy C0014457 Eosinophilia HSDN C0038506 Stutter C0037369 Smoking HSDN C1963091 Diarrhea adverse event C0025269 Multiple endocrine neoplasia type 2b HPO C3463815 Feel fatigue C0006413 Burkitt lymphoma HSDN C4084768 Usual severity vomiting C2586211 Thrombosis of blood vessel HSDN C4085548 Usual severity dizziness C0036439 Scoliosis, unspecified HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006262 Bronchial fistula HSDN C2364111 Gustatory anesthesia C0007785 Cerebral infarction HSDN C0349588 Stature short C0795917 Alpha-thalassemia mental retardation syndrome, deletion-type OrphaNet|HPO|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1866983 Scleroderma, familial progressive MalaCards C4084775 Usual severity weight loss C2674051 Inflammatory bowel disease 11 MalaCards C0033377 Caudal displacement C1096902 Infantile sialic acid storage disease HPO C4084802 Usual severity diarrhea C2239112 Blister dosing unit HSDN C0036396 Sciatica C0024530 Malaria HSDN C2029884 Hearing loss by exam C0029342 Orthomyxoviridae infections HSDN C0030200 Intractable pain C0034067 Pulmonary emphysema HSDN C2984057 Have nausea C0016542 Foreign body HSDN C0151686 Growth retardation C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency OrphaNet C0024031 Back pain lower back C1258666 Myxoid cyst HSDN C4084784 Diarrhea C0376300 Dengue shock syndrome MalaCards C2032395 Pelvic pain on the left C0023890 Liver cirrhosis HSDN C1963252 Tremor adverse event C0040136 Thyroid neoplasm HSDN C2911647 Weight gain adverse event C0016995 Gambling HSDN C4084776 Weight loss C0040715 Chromosomal translocation HSDN C4084727 Cough frequency C0950123 Inborn genetic disease HSDN C0033377 Caudal displacement C1785148 Rapp-hodgkin syndrome HPO C0037771 Paraparesis spastic C1856493 Gaucher disease, norrbottnian type HPO C0030552 Paralysis partial C0032285 Pneumonia HSDN C4085661 Usual severity nausea C0027819 Neuroblastoma HSDN C0162298 Stiffness joints C1854896 Mucolipidosis iii gamma MalaCards|HPO C4084775 Usual severity weight loss C0520946 Emotional hypersensitivity HSDN C2919142 Short stature adverse event C1563720 Kallmann syndrome 2 (disorder) MalaCards|HPO C0018772 Deafness C0026764 Multiple myeloma HSDN C4084784 Diarrhea C2137063 Ent surgical result - speech HSDN C0030794 Pelvis pain C0032966 Complication, neoplastic pregnancy HSDN C2911645 Weight loss adverse event C0023267 Fibroid tumor HSDN C0917816 Deficiency mental C2930923 N-acetylneuraminic acid storage disease MalaCards C0332573 Macula C0265336 Senter syndrome OrphaNet|HPO|MalaCards C0002963 Angina variant C0040156 Thyrotoxicosis HSDN C3665347 Vision impaired C1857618 Achromatopsia 2 MalaCards C0008031 Pain chest C0009375 Colonic neoplasms HSDN C2919142 Short stature adverse event C1834304 Amyotrophy, hereditary neuralgic MalaCards|HPO C0028738 Nystagmus C0265223 Cohen syndrome HPO C0522224 Palsied C0020522 Delayed hypersensitivity HSDN C4085222 Nausea C0026266 Mitral valve insufficiency HSDN C0344315 Mood depressed C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C0031911 Pigment deposition C1857299 Retinal nonattachment, nonsyndromic congenital MalaCards C0026821 Cramp C0036341 Schizophrenia HSDN C0242936 Center pain C0015328 Behavior, exploratory HSDN C0497406 Over weight C0030920 Peptic ulcer HSDN C1963091 Diarrhea adverse event C0003125 Anorexia nervosa HSDN C0020672 Body temperature decreased C0008350 Cholelithiasis HSDN C0002962 Angina C0453996 Tobacco smoking HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1866552 Paragangliomas 2 (disorder) MalaCards C2919142 Short stature adverse event C3809233 Noonan syndrome 8 MalaCards C4085661 Usual severity nausea C0524910 Hepatitis c, chronic MalaCards C1962962 Hyperpigmentation adverse event C1867968 Porphyria cutanea tarda, type i MalaCards C1145670 Failure respiratory C1510455 Acrocephalosyndactylia MalaCards|HPO C0016199 Pain flank C0678051 Adrenocortical carcinoma, stage ii UMLS C2114321 Labor pains preterm C0022876 Premature obstetric labor UMLS C3641756 Have diarrhea C0014179 Endometritis HSDN C4084776 Weight loss C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C0013404 Respiratory difficulty C0031154 Peritonitis HSDN C0000727 Abdomen acute C0010346 Crohn disease HSDN C0026838 Spasticity muscle C0220756 Niemann-pick disease, type c MalaCards|HPO C0018808 Murmur C0039980 Chest injury HSDN C1962972 Proteinuria adverse event C2219717 Menstrual periods stopped for over 6 months HSDN C0007758 Cerebellar ataxia C0078918 Albinism, oculocutaneous HSDN C4085210 Usual severity pain C0015814 Femur head necrosis HSDN C4084776 Weight loss C0162869 Aneurysm, ruptured HSDN C1557397 Adverse event associated with pain C0680727 Mediation HSDN C4084727 Cough frequency C0887976 Chlamydophila infections HSDN C1963137 Hydrocephalus adverse event C0270726 Alexander disease MalaCards|HPO C3898969 Have been vomiting C0038463 Strongyloides infection HSDN C0012833 Dizzy C0013990 Pathological accumulation of air in tissues HSDN C0003862 Pain joint C1866983 Scleroderma, familial progressive MalaCards C4085661 Usual severity nausea C0014836 Escherichia coli infections HSDN C0036396 Sciatica C0023895 Liver diseases HSDN C4084802 Usual severity diarrhea C0014457 Eosinophilia HSDN C2024878 Cardiovascular surgery result: dyspnea C2586211 Thrombosis of blood vessel HSDN C0013390 Cramps menstrual C1706377 Memory device component HSDN C0004941 Behavioral symptoms C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet C4084775 Usual severity weight loss C0009938 Bruising HSDN C1963180 Neck pain adverse event C0039145 Syringomyelia and syringobulbia HSDN C0034124 Pupillary disorder C0014306 Enophthalmos HSDN C0034155 Thrombotic thrombocytopenic purpura C0311468 Increased bilirubin level (finding) HSDN C2911645 Weight loss adverse event C3541994 Drug hypersensitivity syndrome OrphaNet|MalaCards C0010200 Cough symptom C0264456 Copper fever UMLS C4084769 Vomiting frequency C0032066 Plague vaccines HSDN C1527344 Dysphonia C0018523 Hallervorden-spatz syndrome MalaCards|HPO C4085549 Dizziness C0021400 Influenza HSDN C0042963 Symptoms vomiting C0007766 Intracranial aneurysm HSDN C0086437 Joint hypermobility C1834211 Ganglioneuromatosis of the alimentary tract HPO C0026205 Pupillary constriction C0078918 Albinism, oculocutaneous HSDN C4085862 Bothered by nausea C0344315 Depressed mood HSDN C0221752 Rbc urine C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C0413252 Hypothermia due to exposure C0010054 Coronary arteriosclerosis HSDN C0013421 Dystonia C0919524 Atm gene HPO C0349588 Stature short C0340427 Familial dilated cardiomyopathy MalaCards C3146279 Coma C0019195 Hepatitis, viral, human HSDN C2911647 Weight gain adverse event C0702166 Acne HSDN C3812171 Bradycardia by ecg finding C1832411 Ectodermal dysplasia, hidrotic, christianson-fourie type MalaCards C3641756 Have diarrhea C0006114 Cerebral edema HSDN C0015672 Decreased energy C0032851 Disease poultry HSDN C4084724 Usual severity constipation C0039006 Swine--diseases HSDN C4084725 Usual severity cough C0041318 Tuberculosis, meningeal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042961 Intestinal volvulus HSDN C0851578 Disorder sleep C0314657 Genetic predisposition HSDN C2242996 Tingling C2932716 Pseudohypoparathyroidism type 1c HPO C1549543 Administration method - pain C0016470 Food allergy HSDN C0518090 Frequency of pain question C0009021 Clonorchiasis HSDN C0000737 Abdomen pain C0027708 Nephroblastoma OrphaNet|HPO|UMLS C0004134 Dyssynergia C1838979 Mitochondrial complex i deficiency MalaCards|HPO|UMLS C0162298 Stiffness joints C1847593 Epiphyseal dysplasia, multiple, 4 MalaCards C0040822 D tremors C3554398 Spinal muscular atrophy, jokela type MalaCards C0020458 Hyperhydrosis C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C4084767 Bothered by vomiting C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0242936 Center pain C0036974 Shock HSDN C1836296 Lower extremity weakness C1843315 Neuronopathy, distal hereditary motor, type viib HPO C0042755 Virilisation C0852654 21-hydroxylase deficiency MalaCards C0042514 Ventricular tachycardia C3150754 Glycogen storage disease xv MalaCards C1963281 Vomiting adverse event C0019065 Hemorrhage intraperitoneal HSDN C0002624 Amnesia retrograde C0011253 Delusions HSDN C0038868 Supranuclear palsy progressive C0037369 Smoking HSDN C0237326 Defecation pain C0238198 Gastrointestinal stromal tumors OrphaNet|HPO|MalaCards C0557874 Global developmental delay C1833104 Diabetes mellitus, permanent neonatal OrphaNet|HPO|MalaCards C0427055 Face weakness C2936502 Charge syndrome, familial MalaCards C0023380 Lethargy C0393735 Headache disorders HSDN C1963071 Back pain adverse event C1384606 Dyspareunia HSDN C0000727 Abdomen acute C0267941 Pancreatitis, acute necrotizing HSDN C0751495 Seizure focal C0393677 Benign occipital epilepsy of childhood - late onset variant UMLS C0020796 Profoundly mentally retarded C2750798 Polymicrogyria with optic nerve hypoplasia HPO C4084767 Bothered by vomiting C0026782 Mumps vaccine HSDN C4085210 Usual severity pain C0027708 Nephroblastoma HSDN C3665492 Pigmentations C0019569 Hirschsprung disease MalaCards C0240211 Swelling lips C0025235 Melkersson-rosenthal syndrome MalaCards|UMLS C0427055 Face weakness C1839259 Bulbo-spinal atrophy, x-linked UMLS C0012569 Double vision C0002940 Aneurysm HSDN C0013395 Indigestion C0007621 Neoplastic cell transformation HSDN C0557874 Global developmental delay C1832916 Timothy syndrome MalaCards C2315100 Pediatric failure to thrive C0035078 Kidney failure MalaCards C0011206 Delirium acute C0001546 Adjustment disorders HSDN C4084769 Vomiting frequency C0009324 Ulcerative colitis HSDN C2700617 Irritation - emotion C0268560 Hyperglycinemia, transient neonatal HPO C1549543 Administration method - pain C0037413 Social dominance HSDN C2984058 Have pain C0206698 Cholangiocarcinoma HSDN C0151786 Weakness muscle C0221043 Liddle syndrome OrphaNet|HSDN|HPO|MalaCards C0013911 Emaciate C0038463 Strongyloides infection HSDN C3665492 Pigmentations C0152255 Pinguecula MalaCards C3463815 Feel fatigue C3146222 Idiopathic aortitis MalaCards C0042571 Vertigo subjective C0006434 Burn injury HSDN C0424755 Fever symptoms C0015807 Femoral neoplasm HSDN C0018681 Headache, cephalalgia C2973787 Coxiella burnetii infection MalaCards C0026838 Spasticity muscle C0001175 Acquired immunodeficiency syndrome HSDN C0026838 Spasticity muscle C3714509 Nutrition disorders HSDN C2315100 Pediatric failure to thrive C2985290 Fetal alcohol spectrum disorders HSDN C0007758 Cerebellar ataxia C0751955 Brain infarction HSDN C0040485 Wryneck C0012979 Canine disease HSDN C0015469 Facial paralysis C0007133 Carcinoma, papillary HSDN C4084766 Vomiting C0011581 Depressive disorder HSDN C0030193 Sense of pain C0040517 Gilles de la tourette syndrome HSDN C0018681 Headache, cephalalgia C0026946 Mycoses HSDN C0011991 Loose stools C0031149 Peritoneal neoplasms HSDN C0026838 Spasticity muscle C0041327 Tuberculosis, pulmonary HSDN C3665386 Abnormal vision C3711850 Opticospinal multiple sclerosis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0002382 Alveolar bone loss HSDN C0037317 Sleep disturbance C0175694 Smith-lemli-opitz syndrome OrphaNet|MalaCards C2911645 Weight loss adverse event C0013504 Echinococcosis, hepatic HSDN C1963063 Anorexia adverse event C0017536 Giardiasis HSDN C4085549 Dizziness C0029888 Otitis media purulent HSDN C0012833 Dizzy C0338437 Neurocysticercosis HSDN C0242936 Center pain C0030472 Paraneoplastic syndromes HSDN C4084769 Vomiting frequency C1527348 Brain hypoxia HSDN C0019572 Hairiness C0032708 Disorders of porphyrin metabolism HSDN C0851578 Disorder sleep C0023066 Laryngismus HSDN C2024893 Cardiovascular surgery result: fatigue C0021841 Intestinal neoplasms HSDN C0015230 Exanthem C0406319 Sebopsoriasis UMLS C4084774 Have weight loss C0022660 Kidney failure, acute HSDN C0019080 Bleed_nos problem C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C1963091 Diarrhea adverse event C1865145 Congenital disorder of glycosylation type 1b MalaCards|HPO C4084768 Usual severity vomiting C0025007 Measles HSDN C0015468 Face pain C0236969 Substance-related disorders HSDN C0020672 Body temperature decreased C2586211 Thrombosis of blood vessel HSDN C0020615 Hypoglycemia nos C2936915 Amylo-1,6-glucosidase deficiency OrphaNet|HPO C0036572 Convulsion C0152054 Therapeutic touch HSDN C0008031 Pain chest C1334409 Localized adrenal gland pheochromocytoma UMLS C0007166 Cardiac output decreased C0024121 Lung neoplasms HSDN C0028738 Nystagmus C0003076 Aniridia OrphaNet|HPO|MalaCards C0406407 Cholinergic pruritus C0009450 Disease caused by microorganism UMLS C2203646 Jaundice C0011265 Presenile dementia HSDN C0034063 Edema lung C1849813 Glycogen storage disease of heart, lethal congenital MalaCards|HPO C4084776 Weight loss C1546654 Specimen source codes - granuloma HSDN C0000727 Abdomen acute C0018133 Graft-vs-host disease HSDN C0036572 Convulsion C1846172 Hydranencephaly and abnormal genitalia HPO C0019079 Bloody sputum C0038454 Cerebrovascular accident HSDN C0018784 Deafness sensorineural C1835922 Aminoacylase 1 deficiency MalaCards|HPO C0036572 Convulsion C0702221 Tactual discrimination HSDN C1962972 Proteinuria adverse event C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C4084726 Distress cough C0001418 Adenocarcinoma HSDN C0042024 Urine incontinence C0020635 Hypopituitarism HSDN C0349588 Stature short C2675014 Mullerian aplasia and hyperandrogenism OrphaNet|HPO|MalaCards C0038002 Spleen enlargement C0032463 Polycythemia vera OrphaNet|HPO C0026884 Muteness C3266898 Waardenburg syndrome HSDN C0018681 Headache, cephalalgia C0008043 Chiari-frommel syndrome HSDN C1962972 Proteinuria adverse event C2364172 Adherence to medication regime HSDN C0751837 Gait ataxic C1846492 Spinocerebellar ataxia, autosomal recessive 4 MalaCards|UMLS C1971624 Appetite absent C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C4084776 Weight loss C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C1971624 Appetite absent C0460137 Push down or depress HSDN C1963177 Muscle pain adverse event C0080040 Polio post syndrome DiseaseOntology|MalaCards C0010200 Cough symptom C0345960 Giant cell carcinoma of lung UMLS C0027497 Queasy C0021359 Infertility HSDN C0013456 Pain ear C0036095 Salivary gland neoplasms HSDN C0085631 Abnormal excitement C1836706 Hyperthyroidism, nonautoimmune MalaCards C0019079 Bloody sputum C0027697 Nephritis HSDN C0013604 Edematous C0348018 Projections HSDN C0557874 Global developmental delay C0343560 Congenital varicella syndrome MalaCards C4085549 Dizziness C0036690 Septicemia HSDN C0000737 Abdomen pain C1708717 Localized resectable adult hepatocellular carcinoma UMLS C0028081 Night sweat C0014118 Endocarditis UMLS C1971624 Appetite absent C0024115 Lung diseases HSDN C0030552 Paralysis partial C0062527 Hepatitis b vaccine HSDN C4085210 Usual severity pain C0006433 Burnout, professional HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1963106 Esophagitis adverse event HSDN C0030193 Sense of pain C0014866 Esophageal stenosis HSDN C3898969 Have been vomiting C0751161 Udpglucose 4-epimerase deficiency disease MalaCards|HPO C4085222 Nausea C0020473 Hyperlipidemia HSDN C1557397 Adverse event associated with pain C0007279 Carotid body paraganglioma HSDN C4084776 Weight loss C0036330 Schistosomiasis mansoni HSDN C0013362 Dysarthrias C1837541 Spinocerebellar ataxia 20 MalaCards C0030193 Sense of pain C0040997 Trigeminal neuralgia UMLS C4085211 Pain distress question C0027401 Narcissism HSDN C3809715 Epistaxis recurrent C0039445 Hereditary hemorrhagic telangiectasia HPO C0043094 Weight gain C0032310 Pneumonia, viral HSDN C0242936 Center pain C0003723 Arbovirus infections HSDN C0036659 Sensation disorder C0409959 Osteoarthritis, knee HSDN C3146279 Coma C0460137 Push down or depress HSDN C0013404 Respiratory difficulty C4041080 Neurocognitive disorders HSDN C0424755 Fever symptoms C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3641756 Have diarrhea C3809369 Paroxysmal nocturnal hemoglobinuria 2 MalaCards C3641756 Have diarrhea C0022353 Neonatal jaundice HSDN C1962962 Hyperpigmentation adverse event C1851412 Extrasystoles, multiform ventricular, with short stature, hyperpigmentation and microcephaly MalaCards C0878707 Precipitous drop in hematocrit C2729121 Precipitous drop in hemoglobin UMLS C1963249 Tinnitus adverse event C0032963 Pregnancy complications, cardiovascular HSDN C0002962 Angina C0029401 Osteitis deformans HSDN C4085210 Usual severity pain C0026782 Mumps vaccine HSDN C0015672 Decreased energy C0026636 Mouth diseases HSDN C4084724 Usual severity constipation C0025063 Mediastinal neoplasms HSDN C3887873 Hearing loss C0007873 Uterine cervical neoplasm HSDN C4085317 Diarrhea frequency C0040046 Thrombophlebitis HSDN C0003862 Pain joint C0004576 Babesiosis OrphaNet|MalaCards C0020672 Body temperature decreased C0034063 Pulmonary edema HSDN C0242936 Center pain C0019624 Histiocytosis, non-langerhans-cell HSDN C0011991 Loose stools C0018915 Hemangioendothelioma HSDN C0034933 Abnormal reflexes C0033300 Progeria HSDN C0413252 Hypothermia due to exposure C0014859 Esophageal neoplasms HSDN C4084775 Usual severity weight loss C0023530 Leukopenia HSDN C0231528 Muscle pain generalized C0342769 Deficiency dehydrogenase lactate MalaCards C1961131 Cough adverse event C0011875 Diabetic angiopathies HSDN C4085862 Bothered by nausea C0700327 Clinical findings relating to memory HSDN C0030193 Sense of pain C0264681 Angina pectoris syncope anginosa UMLS C0476273 Distress respiratory C0153122 Induced malaria MalaCards C0851578 Disorder sleep C0023220 Leg injury HSDN C1999266 Depression adverse event C0085547 Phenylketonuria, maternal MalaCards|HPO C0578056 Pain of truncal structure C0458225 Lumbar facet syndrome UMLS C3539892 Pelvic pain in front C0242350 Erectile dysfunction HSDN C4085210 Usual severity pain C1836485 Charcot-marie-tooth disease, axonal, type 2a2 (disorder) HPO C4084727 Cough frequency C0220847 C hepatitis virus HSDN C4085210 Usual severity pain C0003827 Art therapies HSDN C0239376 Lower extremity pain C1304205 Neutrophilic urticaria MalaCards C0012833 Dizzy C0376527 Neoplasm, skull base HSDN C4084774 Have weight loss C0238339 Hereditary pancreatitis HSDN C3641756 Have diarrhea C0009021 Clonorchiasis DiseaseOntology C2911647 Weight gain adverse event C0009782 Connective tissue diseases HSDN C0004604 Pain back C0241158 Cicatrix skin HSDN C0036572 Convulsion C0032914 Pre-eclampsia HSDN C0042798 Vision dim C0026598 Movement perception HSDN C4084725 Usual severity cough C0037928 Spinal cord diseases HSDN C0151315 Neck rigid C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0522224 Palsied C0878544 Cardiomyopathies HSDN C2237041 Shox gene with short stature C1853566 Genitopatellar syndrome MalaCards|HPO C0015230 Exanthem C0011311 Dengue fever DiseaseOntology|OrphaNet|MalaCards C0030232 Color loss C0175816 Cold hemagglutinin disease OrphaNet|MalaCards C0002962 Angina C0022568 Keratitis HSDN C0042024 Urine incontinence C0014556 Epilepsy, temporal lobe HSDN C0426579 Anorexia symptom C0022116 Ischemia HSDN C1279888 Proteinuria of undiagnosed cause C0005424 Biliary tract diseases HSDN C0019209 Large liver C1855396 Alpha mannosidosis, type ii HPO C1963249 Tinnitus adverse event C1568248 Usher syndrome, type iii MalaCards C0035078 Failure kidney C0033770 Prune belly syndrome OrphaNet|HPO|MalaCards C1963252 Tremor adverse event C0031149 Peritoneal neoplasms HSDN C4084766 Vomiting C1705810 Generic role HSDN C2362324 Pediatric obesity C0039474 Temperament HSDN C1557397 Adverse event associated with pain C0030482 Paraepithymia HSDN C3641756 Have diarrhea C0085435 Arthritis, reactive OrphaNet|MalaCards C4084774 Have weight loss C0751955 Brain infarction HSDN C4085317 Diarrhea frequency C0038663 Suicide attempt HSDN C0518090 Frequency of pain question C0027401 Narcissism HSDN C0001825 Agraphia C0017636 Glioblastoma HSDN C0010200 Cough symptom C1708650 Laryngeal basaloid carcinoma UMLS C0023530 Leukopenia C0079504 Hermanski-pudlak syndrome OrphaNet|MalaCards C1963087 Constipation adverse event C0749420 Thyroid agenesis HPO C0240715 Perineal lump C0267560 Sentinel tag UMLS C0162834 Hyperpigmentation C0162569 Hepatoerythropoietic porphyria MalaCards C0013604 Edematous C0264005 Fasciitis, eosinophilic OrphaNet|MalaCards C4084773 Bothered by weight gain C0041374 Tumor virus infections HSDN C0013404 Respiratory difficulty C1527336 Sjogren's syndrome HSDN C0042940 Disorder of voice C0051981 Anti-leprosy vaccine HSDN C4084726 Distress cough C1546847 Entity name part type - family HSDN C1963281 Vomiting adverse event C0039128 Syphilis HSDN C0085636 Light sensitivity C0242852 Proliferative vitreoretinopathy HSDN C2165509 Depression accompanied by eating more C0011581 Depressive disorder UMLS C2203646 Jaundice C0010034 Corneal diseases HSDN C1557397 Adverse event associated with pain C0038018 Spondylolysis HSDN C0011991 Loose stools C0025286 Meningioma HSDN C0557874 Global developmental delay C0268547 Argininosuccinic aciduria MalaCards|HPO C0518090 Frequency of pain question C0036039 Sadism HSDN C0036572 Convulsion C0553580 Ewings sarcoma HSDN C0234132 Pyramidal sign C1836295 Spastic paraplegia 28, autosomal recessive (disorder) MalaCards|UMLS C4085317 Diarrhea frequency C0018995 Hemochromatosis HSDN C0240735 Personality change C1868594 Perry syndrome MalaCards|HPO C0151686 Growth retardation C1313961 Trichorrhexis nodosa syndrome MalaCards C0522224 Palsied C0022593 Keratosis HSDN C2919142 Short stature adverse event C3151113 Meier-gorlin syndrome 3 MalaCards C0878752 Abnormal loss of weight and underweight C0497409 Other nutritional; endocrine; and metabolic disorders UMLS C1963086 Confusion adverse event C0011551 Depersonalisation HSDN C1279888 Proteinuria of undiagnosed cause C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0011168 Disorder deglutition C2931107 Myasthenic syndrome, congenital, postsynaptic slow-channel MalaCards|HPO C0424755 Fever symptoms C0009373 Colonic diseases HSDN C2984058 Have pain C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C0349588 Stature short C1832648 Hypoparathyroidism familial isolated OrphaNet|MalaCards C0040034 Thrombocytopenia C0032749 Post-kala-azar dermal leishmaniasis MalaCards C0015230 Exanthem C0018572 Hand, foot and mouth disease UMLS C0270948 Neurogenic muscular atrophy C1848029 Ehlers-danlos syndrome caused by tenascin-x deficiency OrphaNet|HPO C4049644 Depression C2930674 Babesioses, human MalaCards C0018991 Paralysis one side of body C0008370 Cholestasis HSDN C0857119 Hesitancy/poor urinary stream C0152032 Hesitancy urination UMLS C0020438 Hypercalciuria C0006663 Calcinosis HSDN C0018681 Headache, cephalalgia C0034885 Rectal neoplasms HSDN C0476273 Distress respiratory C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal HPO|UMLS C2203646 Jaundice C2931132 Crigler najjar syndrome, type 2 MalaCards C0314719 Dry eyes C0856141 Dry eyes aggravated UMLS C2096293 Ent surgical result ear vertigo C0013806 Electroplexy shock therapy HSDN C0022346 Yellow skin C0006434 Burn injury HSDN C0020903 Illusion C0524528 Pervasive development disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036117 Salmonella infections HSDN C2919142 Short stature adverse event C0022441 Juvenile osteochondrosis of hip MalaCards C0575081 Abnormal gait C0238286 Mucolipidosis type iv OrphaNet|HPO|MalaCards C0700078 Deep tendon reflex decrease C1837552 Charcot-marie-tooth disease, axonal, type 2l (disorder) MalaCards|HPO C0022346 Yellow skin C0029118 Opportunistic infections HSDN C0000727 Abdomen acute C3489393 Hiatal hernia HSDN C0026858 Musculoskeletal pain C3887650 Adult rickets HSDN C0012833 Dizzy C0395947 Autoimmune disorder ear inner UMLS C0575081 Abnormal gait C1855128 Methylcobalamin deficiency, cblg type MalaCards|HPO C0029163 Hemorrhage mouth C0011406 Dental pulp exposure HSDN C0007166 Cardiac output decreased C0011570 Mental depression HSDN C0030193 Sense of pain C0004144 Atelectasis HSDN C0233773 Hallucinations hypnogogic C0751362 Narcolepsy-cataplexy syndrome MalaCards C0413252 Hypothermia due to exposure C4084909 Depression subordinate domain HSDN C0242936 Center pain C0022353 Neonatal jaundice HSDN C3898969 Have been vomiting C0019285 Diaphragmatic hernia traumatic HSDN C0018834 Brash C0796117 Pitt syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0029400 Osteitis HSDN C0009676 Confusion state C1457883 Aggressive reaction HSDN C4084776 Weight loss C0342257 Complications of diabetes mellitus HSDN C0020538 Hbp C3665770 Acquired lipoatrophic diabetes MalaCards C1963249 Tinnitus adverse event C3850024 Transcranial direct current stimulation HSDN C3541349 Syncope C0033817 Pseudomonas infections HSDN C0040034 Thrombocytopenia C0549463 X-linked lymphoproliferative disorder MalaCards C1557397 Adverse event associated with pain C0032994 Pregnancy, tubal HSDN C0030552 Paralysis partial C0595812 Fistula route HSDN C4084774 Have weight loss C0033054 Prenatal exposure delayed effects HSDN C0917816 Deficiency mental C4014343 Mental retardation, autosomal recessive 42 MalaCards C0917816 Deficiency mental C0410539 Craniodiaphyseal dysplasia OrphaNet|HPO|MalaCards C3203358 Alveolar hypoventilation C0030330 Panniculitis, peritoneal HSDN C1963091 Diarrhea adverse event C0029182 Orbit (eye disorders) HSDN C0349588 Stature short C3537440 Cystinosis, infantile nephropathic MalaCards C1510417 Apraxia of gait C0009241 Cognition disorders HSDN C4084767 Bothered by vomiting C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C2984058 Have pain C0001429 Adenolymphoma HSDN C0019825 Voice hoarseness C0030442 Progressive bulbar palsy HSDN C4084802 Usual severity diarrhea C0002726 Amyloidosis HSDN C0018808 Murmur C0023569 Levocardia HSDN C0023015 Language handicap C0265499 49,xxxxy chromosomal anomaly OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0566602 Primary sclerosing cholangitis MalaCards|HPO C0015970 Fever unknown origin C0039483 Giant cell arteritis HSDN C0018784 Deafness sensorineural C0025284 Meningeal neoplasms HSDN C3274924 Have been coughing C0019557 Hip fx HSDN C0027498 Nausea vomiting C1290613 Disease of upper gastrointestinal tract UMLS C0011991 Loose stools C0268225 Aspartylglucosaminuria MalaCards|HPO|UMLS C0030193 Sense of pain C0001828 Agricultural workers' diseases HSDN C0518090 Frequency of pain question C0151814 Coronary occlusion HSDN C0032617 High urine output C0205734 Diabetes, autoimmune MalaCards C0030554 Abnormal sensation C0011854 Diabetes mellitus, insulin-dependent HSDN C1963086 Confusion adverse event C0085209 Bovine spongiform encephalitis MalaCards C0853986 Lymphocytes decreased C1860168 Achondroplasia, so-called, and severe combined immunodeficiency OrphaNet|MalaCards C0542476 Forgetful C1836383 Spinocerebellar ataxia 27 HPO C4084725 Usual severity cough C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive OrphaNet|MalaCards C0013604 Edematous C0024535 Malaria, falciparum HSDN C0020580 Decreased sensation C0546952 Congenital facial asymmetry HSDN C4084773 Bothered by weight gain C0015923 Fetal alcohol syndrome HSDN C0022346 Yellow skin C0019372 Herpesviridae infections HSDN C4084773 Bothered by weight gain C0030767 Grouping peer HSDN C0011168 Disorder deglutition C2931347 Cardiac form of generalized glycogenosis MalaCards C4084775 Usual severity weight loss C0264005 Fasciitis, eosinophilic MalaCards C1860844 Sparse, thin hair C3281289 Trichohepatoenteric syndrome 2 MalaCards|UMLS C1557397 Adverse event associated with pain C0678236 Rare diseases HSDN C0232466 Feeding difficulty C0796200 Wieacker-wolff syndrome MalaCards C0264272 Nose discharge, purulent C0021368 Inflammation UMLS C0043094 Weight gain C1963064 Anxiety adverse event HSDN C0030552 Paralysis partial C0039984 Thoracic outlet syndrome OrphaNet|HSDN|MalaCards C0015402 Hemorrhage eye C0751795 Head injury penetrating HSDN C0151786 Weakness muscle C1384514 Conn syndrome MalaCards C0518090 Frequency of pain question C0011606 Exfoliative dermatitis HSDN C3641755 Have constipation C0012359 Pathological dilatation HSDN C2984057 Have nausea C3809609 Primary aldosteronism, seizures, and neurologic abnormalities MalaCards C0027066 Myoclonic jerking C0030463 Paramyoclonus multiplex UMLS C1962972 Proteinuria adverse event C0001768 Agammaglobulinemia HSDN C0018772 Deafness C0162429 Malnutrition HSDN C0032285 Pneum C3554686 Immunodeficiency 11 MalaCards C0037317 Sleep disturbance C2930798 Alexanders leukodystrophy MalaCards C0018991 Paralysis one side of body C0034530 Injury radiation HSDN C0023015 Language handicap C0008096 Children exceptional HSDN C4085317 Diarrhea frequency C0019202 Hepatolenticular degeneration HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011854 Diabetes mellitus, insulin-dependent HSDN C1963184 Nystagmus adverse event C2936741 Syndrome xxyy MalaCards C0009080 Finger clubbing C0264511 Lymphoid interstitial pneumonia MalaCards C0270948 Neurogenic muscular atrophy C3151403 Amyotrophic lateral sclerosis 14 with or without frontotemporal dementia HPO C4042891 Sleep wake disorders C0022865 Obstetric labor complications HSDN C1145670 Failure respiratory C2931854 Allergic bronchopulmonary mycosis MalaCards C1963071 Back pain adverse event C0001175 Acquired immunodeficiency syndrome HSDN C4084784 Diarrhea C1962974 Chylothorax adverse event HSDN C0018784 Deafness sensorineural C0010308 Congenital hypothyroidism HSDN C0162834 Hyperpigmentation C0036489 Sea-blue histiocyte syndrome MalaCards|HPO C0030554 Abnormal sensation C1260409 Myasthenia gravis without acute exacerbation MalaCards C4084775 Usual severity weight loss C1555914 Psychologist - psychotherapy, group HSDN C3829611 Nausea frequency C0027765 Nervous system disorder HSDN C4085317 Diarrhea frequency C2364172 Adherence to medication regime HSDN C0033377 Caudal displacement C1852267 Optic atrophy 1 and deafness HPO C0700590 Diaphoresis excessive C3146222 Idiopathic aortitis MalaCards C0557874 Global developmental delay C0338503 Septo-optic dysplasia MalaCards|HPO C3494358 Characteristic, prodromal C0742343 Acute chest syndrome HSDN C4085210 Usual severity pain C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C1963091 Diarrhea adverse event C0021053 Immune system diseases HSDN C4084775 Usual severity weight loss C0020522 Delayed hypersensitivity HSDN C0234132 Pyramidal sign C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0015468 Face pain C0038160 Staphylococcal infections HSDN C0018784 Deafness sensorineural C3806702 Charcot-marie-tooth disease, x-linked dominant, 6 MalaCards C0151889 Reflexes tendon increased C1857568 Cortical blindness, retardation, and postaxial polydactyly OrphaNet|MalaCards C0018681 Headache, cephalalgia C2945560 Hemolytic HSDN C0009421 Comatose C0027643 Neoplasm recurrence, local HSDN C0042940 Disorder of voice C0011265 Presenile dementia HSDN C0234376 Tremor action C3887678 Cpnet MalaCards C0002622 Amnesias C0011570 Mental depression HSDN C0011991 Loose stools C0032987 Ectopic pregnancy HSDN C0038990 Sweats C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0022346 Yellow skin C0001175 Acquired immunodeficiency syndrome HSDN|UMLS C0151786 Weakness muscle C2930812 Generalized elastolysis MalaCards C4084774 Have weight loss C0919691 Anastomotic leaks HSDN C0018834 Brash C4049644 Depression HSDN C3665386 Abnormal vision C0220633 Uveal melanoma OrphaNet|HPO C0011570 Monopolar depression C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C0027796 Neuralgias C0002871 Anemia HSDN C0237326 Defecation pain C0268322 Chester-type porphyria HPO C0013604 Edematous C0341106 Eosinophilic esophagitis OrphaNet|MalaCards C1962956 Flatulence adverse event C0344315 Depressed mood HSDN C0850758 Pain pelvic C0038160 Staphylococcal infections HSDN C0019079 Bloody sputum C0162316 Iron deficiency anemia HSDN C1069915 Vertigo C1836438 Familial neurocardiogenic syncope MalaCards C0013528 Echo speech C1704770 Nci thesaurus association HSDN C3898969 Have been vomiting C0003047 Animal disease HSDN C0013604 Edematous C0015814 Femur head necrosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0518450 Spinal fractures HSDN C0020450 Hyperemesis gravidarum C0008925 Cleft palate HSDN C0241237 Standing difficulty C0342646 Vitamin d-dependent rickets, type 2a HPO|UMLS C0013604 Edematous C3714509 Nutrition disorders HSDN C0002962 Angina C0029408 Degenerative polyarthritis HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0497327 Dementia HSDN C0231341 Aging premature C0016325 Fluoride intoxication HSDN C4085548 Usual severity dizziness C3827868 Tachycardia by ecg finding HSDN C4084767 Bothered by vomiting C0007001 Carbohydrate metabolism, inborn errors HSDN C0037763 Spasm C0032851 Disease poultry HSDN C0036572 Convulsion C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0000737 Abdomen pain C0008384 Cholesterol ester storage disease HSDN C0030554 Abnormal sensation C0038436 Post-traumatic stress disorder HSDN C0577294 Perianal mass C0267560 Sentinel tag UMLS C0518090 Frequency of pain question C0007774 Cerebral arterial diseases HSDN C0151786 Weakness muscle C0268242 Niemann-pick disease, type a MalaCards|HSDN|HPO|UMLS C0518090 Frequency of pain question C1254288 Anthrax HSDN C0518090 Frequency of pain question C0043395 Yellow fever HSDN C0019825 Voice hoarseness C1266119 Solitary fibrous tumor HSDN C4084784 Diarrhea C0836924 Thrombocytosis HSDN C2219946 Sleep terrors with poor dream recall C0037320 Night terrors UMLS C0270948 Neurogenic muscular atrophy C0268365 Marfanoid hypermobility syndrome MalaCards C3494358 Characteristic, prodromal C0871740 Face perception HSDN C1961131 Cough adverse event C0020523 Immediate hypersensitivity HSDN C0018991 Paralysis one side of body C0702094 Agranulocytosis lab result HSDN C0398650 Idiopathic thrombocytopenia purpura C0042138 Uterine neoplasms HSDN C1860844 Sparse, thin hair C0079583 Ichthyosiform erythroderma, congenital MalaCards C0018991 Paralysis one side of body C3887532 Ulceration HSDN C0150055 Pain chronic C0027651 Tumor HSDN C0000737 Abdomen pain C0036864 Sexual relations HSDN C4085211 Pain distress question C0036429 Sclerosis HSDN C0150055 Pain chronic C0014836 Escherichia coli infections HSDN C2911645 Weight loss adverse event C0003496 Aortic rupture HSDN C0010200 Cough symptom C1334680 Mediastinal seminoma UMLS C0018681 Headache, cephalalgia C1548578 Location characteristic id - smoking HSDN C0243026 Generalized infection C0221023 Cyclic neutropenia OrphaNet|HPO C0026603 Motion sickness C0007297 Car sickness MalaCards C0042571 Vertigo subjective C0395941 Cochlear dysplasia mondini defect UMLS C0030193 Sense of pain C1301339 Extraovarian endometriosis UMLS C0013362 Dysarthrias C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C3887873 Hearing loss C0006131 Branchioma HSDN C1963091 Diarrhea adverse event C0697038 Asclepias tuberosa HSDN C0700078 Deep tendon reflex decrease C2750798 Polymicrogyria with optic nerve hypoplasia HPO C0002962 Angina C0012739 Disseminated intravascular coagulation HSDN C0007758 Cerebellar ataxia C1858804 Cerebellar ataxia, deafness, and narcolepsy HPO C0002962 Angina C0014743 Erythema nodosum HSDN C1963071 Back pain adverse event C0017658 Glomerulonephritis HSDN C1963091 Diarrhea adverse event C0014547 Epilepsies, partial HSDN C1557397 Adverse event associated with pain C0008732 Chylous ascites HSDN C3665492 Pigmentations C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0030486 Extremity paralysis, lower C0019625 Sinus histiocytosis MalaCards|HSDN C0037384 Snore C1999266 Depression adverse event HSDN C1963091 Diarrhea adverse event C0020542 Pulmonary hypertension HSDN C1263846 Attention deficit disorder with hyperactivity C0034013 Precocious puberty MalaCards C0344435 Ventricular fibrillation by ecg finding C1142166 Brugada syndrome (disorder) HPO C2024878 Cardiovascular surgery result: dyspnea C3151264 Cardiomyopathy, familial hypertrophic, 17 HPO C0018681 Headache, cephalalgia C0016045 Fibroma HSDN C0264588 Dysphonia spasmodic C1837541 Spinocerebellar ataxia 20 MalaCards C0460137 Push down or depress C0265216 X-linked hydrocephalus syndrome MalaCards C0018991 Paralysis one side of body C0027927 Neurosyphilis HSDN C0038506 Stutter C3494322 Narrative therapy HSDN C0242936 Center pain C0031142 Peritoneal diseases HSDN C0263629 Tumor-like lesions of the skin C0349502 Cutaneous dermoid cyst UMLS C3829611 Nausea frequency C0020542 Pulmonary hypertension HSDN C0030193 Sense of pain C1332982 Childhood mesenchymal chondrosarcoma UMLS C0795692 Lactate blood increased C0220981 Metabolic acidosis HSDN C0020673 Hypothermia (central) (local) C0597109 Nurse's role HSDN C0036572 Convulsion C0438418 Visual reflex epilepsy UMLS C0151889 Reflexes tendon increased C2674766 Myokymia 1 HPO C4084776 Weight loss C0473876 Cryptogenic tularaemia MalaCards C0026838 Spasticity muscle C1848412 Trichothiodystrophy with sun sensitivity HPO C0042571 Vertigo subjective C0038395 Streptococcal infections HSDN C0035232 Diaphragmatic paralysis C0697038 Asclepias tuberosa HSDN C0028738 Nystagmus C1859194 Griscelli syndrome, type 1 OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C3813607 Infantile gastroesophageal reflux HSDN C0043094 Weight gain C0011168 Deglutition disorders HSDN C0042024 Urine incontinence C0032966 Complication, neoplastic pregnancy HSDN C4042891 Sleep wake disorders C0016658 Fracture bone HSDN C0040822 D tremors C0037773 Spastic paraplegia, hereditary HSDN C1557397 Adverse event associated with pain C0005424 Biliary tract diseases HSDN C3829611 Nausea frequency C0848377 Trauma to the abdomen HSDN C4084802 Usual severity diarrhea C0015671 Father HSDN C0031911 Pigment deposition C1832661 Anophthalmia and pulmonary hypoplasia MalaCards C0015970 Fever unknown origin C0004669 Bacteroides infections HSDN C1963091 Diarrhea adverse event C0018939 Hematological disease HSDN C0037763 Spasm C0595812 Fistula route HSDN C0015469 Facial paralysis C0039128 Syphilis HSDN C0476478 Demoralisation and apathy C0003469 Anxiety disorders UMLS C2141922 Pain in left hip C0810350 Non-traumatic joint disorders UMLS C0033774 Skin pruritus C0021295 Infant, premature, diseases HSDN C3815497 Cough C0268243 Niemann-pick disease, type b HSDN C0042963 Symptoms vomiting C3495422 Finding relating to sexuality and sexual activity HSDN C0016927 Gag reflex C0517960 Neurological status: consciousness HSDN C4084766 Vomiting C1367460 Lats1 gene HSDN C4084784 Diarrhea C0993582 Arthritis, experimental HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0018939 Hematological disease HSDN C0018780 Frequencies hearing high loss C2675236 Deafness, autosomal dominant 2b MalaCards|HPO C0000727 Abdomen acute C0151744 Myocardial ischemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0030552 Paralysis partial C0268238 Triglyceride storage disease with ichthyosis MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0005940 Bone diseases HSDN C0013604 Edematous C0023892 Biliary cirrhosis HSDN C0018772 Deafness C3711158 Metatropic dwarfism, type ii MalaCards C4084769 Vomiting frequency C0342793 Malonic aciduria MalaCards|HPO C0332573 Macula C1333088 Colonic hamartomatous polyps MalaCards C1963137 Hydrocephalus adverse event C2931764 Furlong syndrome MalaCards C0015468 Face pain C0027859 Acoustic neuroma HSDN C2919142 Short stature adverse event C4014479 Culler-jones syndrome MalaCards C0031911 Pigment deposition C1883486 Uterine corpus cancer MalaCards C0231529 Pain tendon C0920065 Achilles tendon pain UMLS C1279888 Proteinuria of undiagnosed cause C0039082 Syndrome HSDN C4084767 Bothered by vomiting C0020428 Hyperaldosteronism HSDN C0032617 High urine output C0080274 Urinary retention HSDN C1963091 Diarrhea adverse event C0027412 Opioid-related disorders HSDN C0917801 Sleep disorder insomnia C0393760 Trouble falling asleep UMLS C2919142 Short stature adverse event C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C0424755 Fever symptoms C0002514 Amino acid metabolism, inborn errors HSDN C0036572 Convulsion C0026946 Mycoses HSDN C0234253 Rest pain C2104679 Monckeberg's arteriosclerosis with rest pain UMLS C2919142 Short stature adverse event C1845167 Dent disease 2 MalaCards|HPO C1962972 Proteinuria adverse event C0017185 Gastrointestinal neoplasms HSDN C1069915 Vertigo C1527336 Sjogren's syndrome HSDN C1963065 Apnea adverse event C0035353 Retrognathia HSDN C0270846 Astatic seizure C1969810 Febrile convulsions, familial, 8 HPO C1999266 Depression adverse event C1868596 Atypical parkinson disease HPO C0010200 Cough symptom C0032131 Plasmacytoma HSDN C0518090 Frequency of pain question C0867389 Chronic graft-versus-host disease MalaCards C2936821 Spinal cerebrospinal fluid leak C0028850 Ocular motility disorders HSDN C0151786 Weakness muscle C0002736 Amyotrophic lateral sclerosis MalaCards C0020672 Body temperature decreased C0018809 Heart neoplasm HSDN C0013144 Drowsy C1837454 Spinocerebellar ataxia 8 MalaCards C0427068 Legs weakness C1839264 Spastic paraplegia 2, x-linked (disorder) MalaCards|HPO C2132198 Abnormal blistering of the skin C0010495 Cutis laxa MalaCards C0086565 Liver function abnormal C3150802 Myopathy, lactic acidosis, and sideroblastic anemia 2 MalaCards|HPO C0039070 Collapse fleeting C1552262 Nurse practitioner - family HSDN C0040485 Wryneck C0040136 Thyroid neoplasm HSDN C0030554 Abnormal sensation C1856058 Homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity HPO C1850830 Exercise-induced muscle pain C1850674 Minicore myopathy with external ophthalmoplegia (disorder) MalaCards|HPO|UMLS C0042963 Symptoms vomiting C2240374 Eosinophil count raised HSDN C3829611 Nausea frequency C0036864 Sexual relations HSDN C3274924 Have been coughing C0206138 Crest syndrome MalaCards C4084769 Vomiting frequency C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0221232 Welts C1304182 Allergic angio-oedema due to ingested food UMLS C0027796 Neuralgias C0040457 Tooth, supernumerary HSDN C4085549 Dizziness C0027663 Neoplasms, multiple primary HSDN C0241210 Speaking delay C3150675 Chromosome 15q24 duplication syndrome HPO C0424755 Fever symptoms C0003507 Aortic valve stenosis HSDN C0036572 Convulsion C0524910 Hepatitis c, chronic HSDN C1962972 Proteinuria adverse event C0008065 Childhood behavior HSDN C0042963 Symptoms vomiting C0341480 Pancreas, cyst, congenital MalaCards C0003113 Anomia C1963107 Euphoria adverse event HSDN C0027796 Neuralgias C0022865 Obstetric labor complications HSDN C4084723 Constipation C3827868 Tachycardia by ecg finding HSDN C2984058 Have pain C0023891 Liver cirrhosis, alcoholic HSDN C1963180 Neck pain adverse event C0022661 Kidney failure, chronic HSDN C4084767 Bothered by vomiting C0014547 Epilepsies, partial HSDN C2984058 Have pain C0008698 Maxillary sinusitis chronic HSDN C2881383 Sudden visual loss, right eye C0809996 Blindness and vision defects UMLS C0085642 Asphyxia reticularis C2347126 Microscopic polyarteritis HSDN C0497406 Over weight C0851578 Sleep disorders UMLS C0557874 Global developmental delay C1834877 Holoprosencephaly 2 (disorder) HPO C0015300 Ocular proptosis C0795889 Allan-herndon-dudley syndrome (ahds) MalaCards|HPO C4084769 Vomiting frequency C0043515 Zollinger-ellison syndrome HSDN C0232466 Feeding difficulty C3554004 Pbd13a MalaCards C0587047 Mass of trunk C0026684 Mucocele of appendix UMLS C0013604 Edematous C1961100 Erectile dysfunction adverse event HSDN C0035229 Respiratory function impaired C0020807 Pulmonary hemosiderosis idiopathic MalaCards C0007758 Cerebellar ataxia C1720983 Channelopathies HSDN C4084766 Vomiting C0033906 Psychological theories HSDN C0522224 Palsied C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162836 Hidradenitis suppurativa HSDN C4085210 Usual severity pain C0036421 Systemic scleroderma HSDN C0162834 Hyperpigmentation C1510415 Osteosclerotic myeloma MalaCards C0349588 Stature short C0265376 Fetal methyl mercury syndrome OrphaNet C2242996 Tingling C0016053 Fibromyalgia HSDN C0030552 Paralysis partial C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C2911645 Weight loss adverse event C0376545 Hematologic neoplasms HSDN C4085210 Usual severity pain C0206488 Peer review, health care HSDN C0018772 Deafness C0011142 Defense mechanism HSDN C4084767 Bothered by vomiting C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C0233794 Memory impaired C2931918 Transketolase defect MalaCards C0018772 Deafness C1864002 Gracile syndrome (disorder) OrphaNet|HPO|MalaCards C4085211 Pain distress question C1253943 Fluid in the chest HSDN C0004134 Dyssynergia C0033860 Psoriasis HSDN C1963170 Hypothermia adverse event C0796561 Melanoma vaccines HSDN C0042798 Vision dim C1867451 Pseudoxanthoma elasticum, heterozygous HPO C1961131 Cough adverse event C0206171 Community acquired infections HSDN C0518090 Frequency of pain question C0282687 Hemorrhagic fever, ebola HSDN C3887638 Failure to thrive in infant C0018818 Ventricular septal defects HSDN C0013404 Respiratory difficulty C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C4085211 Pain distress question C0028433 Nose neoplasms HSDN C1963170 Hypothermia adverse event C3541306 Plasmodium measurement HSDN C1279888 Proteinuria of undiagnosed cause C0036117 Salmonella infections HSDN C0410919 Foetal bradycardia C0428977 Bradycardia UMLS C0018772 Deafness C0031900 Pierre robin syndrome HSDN C0518090 Frequency of pain question C0033806 Pseudohypoparathyroidism HSDN C0025287 Meningitis-like C0025149 Medulloblastoma HSDN C4084725 Usual severity cough C0011581 Depressive disorder HSDN C0013395 Indigestion C0008350 Cholelithiasis HSDN C0004093 Asthenia C0013364 Dysautonomia, familial HSDN C0042963 Symptoms vomiting C0035801 Diseases rodent HSDN C4084784 Diarrhea C0267662 Congenital chloride diarrhea MalaCards|HPO C4085211 Pain distress question C0023524 Leukoencephalopathy, progressive multifocal HSDN C4084726 Distress cough C2242987 Benign mastocytoma MalaCards C0031911 Pigment deposition C0004135 Ataxia telangiectasia MalaCards C4085549 Dizziness C0042338 Herpesvirus 3, human HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0042138 Uterine neoplasms HSDN C0023380 Lethargy C1848553 Homocystinuria, cbld type, variant 1 HPO C0018784 Deafness sensorineural C1333359 Ercc5 gene HSDN C1963086 Confusion adverse event C0012979 Canine disease HSDN C2024893 Cardiovascular surgery result: fatigue C0019112 Hemorrhoids HSDN C0028081 Night sweat C0023281 Leishmaniasis OrphaNet|MalaCards C3641756 Have diarrhea C0040034 Thrombocytopenia HSDN C0037771 Paraparesis spastic C0752160 Hemangioma, cavernous, central nervous system HSDN C0035229 Respiratory function impaired C0024507 Majewski syndrome MalaCards C0015468 Face pain C0031099 Periodontitis HSDN C2237041 Shox gene with short stature C2751608 Pituitary hormone deficiency, combined, 1 MalaCards|HPO C0242936 Center pain C0020258 Hydrocephalus, normal pressure HSDN C0035078 Failure kidney C0403557 Glomerulopathy with giant fibrillar deposits MalaCards C4255193 Bilateral vestibulopathy C3149566 Deafness, autosomal dominant, without vestibular involvement HPO C2700617 Irritation - emotion C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0042025 Urinary incontinence stress C0520946 Emotional hypersensitivity HSDN C1000483 Genus anemia C0028860 Oculocerebrorenal syndrome HPO C4085642 Level of joint stiffness C1838625 Warburg sjo fledelius syndrome OrphaNet|HPO C0476273 Distress respiratory C1852406 Cutis gyrata syndrome of beare and stevenson OrphaNet|UMLS|HPO|MalaCards C0027796 Neuralgias C1704272 Benign prostatic hyperplasia HSDN C0003862 Pain joint C1961835 Gaucher disease, type 1 MalaCards C0030552 Paralysis partial C2931842 Diaphyseal dysplasia 1, progressive MalaCards|HPO C4084802 Usual severity diarrhea C0013418 Abnormal labor HSDN C3665347 Vision impaired C1850994 Foveal hypoplasia with anterior segment anomalies HPO C4084723 Constipation C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C0023014 Developmental disorder language C0030567 Parkinson disease HSDN C4084775 Usual severity weight loss C1861848 Paragangliomas 4 MalaCards C4084767 Bothered by vomiting C0162872 Aortic aneurysm, thoracic HSDN C0751093 Dystonia, limb C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO|UMLS C0221263 Cafe au lait spot C0016064 Fibrous dysplasia, monostotic HSDN C0024312 Lymphocytopenia C2931087 Achondroplasia and swiss type agammaglobulinemia OrphaNet|MalaCards C3463815 Feel fatigue C0001144 Acne vulgaris HSDN C0751837 Gait ataxic C4012790 Ataxia-telangiectasia-like disorder 1 UMLS C0026838 Spasticity muscle C2931828 Keratoderma and spastic paralysis MalaCards C0000737 Abdomen pain C0524909 Hepatitis b, chronic MalaCards|HSDN C0018926 Emesis bloody C0011168 Deglutition disorders HSDN C4084723 Constipation C0024668 Mammary neoplasms, experimental HSDN C3274924 Have been coughing C0524910 Hepatitis c, chronic HSDN C4085210 Usual severity pain C0836924 Thrombocytosis HSDN C1961131 Cough adverse event C0032227 Pleural effusion disorder HSDN C0018772 Deafness C0042373 Vascular diseases HSDN C2911645 Weight loss adverse event C0566602 Primary sclerosing cholangitis OrphaNet|HPO|MalaCards C0036572 Convulsion C3536561 Benign rolandic epilepsy, non-refractory UMLS C0007859 Pain neck C0032586 Polyradiculopathy HSDN C0036659 Sensation disorder C0003873 Rheumatoid arthritis HSDN C2919142 Short stature adverse event C0033300 Progeria OrphaNet|HPO C1384666 Decreased hearing C0812393 Cancer patients and suicide and depression HSDN C4085211 Pain distress question C0282687 Hemorrhagic fever, ebola HSDN C1963065 Apnea adverse event C2609414 Acute kidney injury HSDN C0042963 Symptoms vomiting C0033054 Prenatal exposure delayed effects HSDN C3146279 Coma C0020732 Iatrogenic disease HSDN C1549543 Administration method - pain C0041234 Chagas disease HSDN C2984057 Have nausea C2711266 Infection by anisakis larva MalaCards C0007758 Cerebellar ataxia C0268237 Cytochrome-c oxidase deficiency MalaCards|HSDN|HPO C4084767 Bothered by vomiting C0003469 Anxiety disorders HSDN C0034124 Pupillary disorder C0008297 Choanal atresia HSDN C0040264 Ear ringing sound C0011581 Depressive disorder HSDN C4085211 Pain distress question C0012691 Dislocations HSDN C3541349 Syncope C0026640 Mouth neoplasms HSDN C0015230 Exanthem C0030807 Pemphigus, nos UMLS C0030193 Sense of pain C0016483 Food preferences HSDN C0037763 Spasm C0423738 Levator syndrome UMLS C4084775 Usual severity weight loss C0001430 Adenoma HSDN C3641756 Have diarrhea C0005891 Bodies image HSDN C4084769 Vomiting frequency C1855115 Methylmalonic aciduria, mut(0) type HPO C3641755 Have constipation C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0206146 Myocardial stunning C0003850 Arteriosclerosis HSDN C0004134 Dyssynergia C1963138 Hypertension adverse event HSDN C4084768 Usual severity vomiting C0348018 Projections HSDN C0009676 Confusion state C0025284 Meningeal neoplasms HSDN C1579931 Depressed - symptom C1856492 Gaucher disease, type iiib HPO C1963184 Nystagmus adverse event C1866636 Charcot-marie-tooth disease, type 4c MalaCards|HPO C1069915 Vertigo C3541306 Plasmodium measurement HSDN C0040822 D tremors C2827407 Infectious otitis media HSDN C4085661 Usual severity nausea C0036974 Shock HSDN C1961131 Cough adverse event C0011849 Diabetes mellitus HSDN C0917816 Deficiency mental C0268611 Arakawa syndrome 2 MalaCards C4084727 Cough frequency C0162316 Iron deficiency anemia HSDN C0234146 Absent reflex C1833219 Charcot-marie-tooth disease, axonal, type 2b (disorder) HPO C4084726 Distress cough C0038325 Stevens-johnson syndrome HPO C4084802 Usual severity diarrhea C0039336 Gustatory sense HSDN C4084723 Constipation C0001580 Adolescent behavior HSDN C1384666 Decreased hearing C0008625 Chromosome aberrations HSDN C0036572 Convulsion C0023067 Laryngitis HSDN C0020672 Body temperature decreased C0025284 Meningeal neoplasms HSDN C0024031 Back pain lower back C0032227 Pleural effusion disorder HSDN C0151908 Dry skin C1860224 Ablepharon-macrostomia syndrome OrphaNet|UMLS|HPO|MalaCards C0043094 Weight gain C0023267 Fibroid tumor HSDN C0037763 Spasm C0017181 Gastrointestinal hemorrhage HSDN C0178417 Anhedonia C0149940 Sciatic neuropathy HSDN C0004093 Asthenia C0027821 Syndrome effort UMLS C4084764 Shortness of breath C0155877 Allergic asthma DiseaseOntology C0454644 Delayed language development C0795832 9p tetrasomy OrphaNet|MalaCards C0851578 Disorder sleep C0006430 Burning mouth syndrome HSDN C0030193 Sense of pain C1962976 Ventricular fibrillation adverse event HSDN C0030552 Paralysis partial C1962971 Myocarditis adverse event HSDN C4085317 Diarrhea frequency C1546635 Specimen source codes - fistula HSDN C0030218 Palatal paralysis C0270788 Paralytic syndrome UMLS C0012833 Dizzy C0031090 Periodontal diseases HSDN C0013362 Dysarthrias C1849128 Spastic paraplegia 15, autosomal recessive MalaCards|HPO C2228534 Excessive weight gain during second pregnancy C0269672 Weight gain pregnancy excessive UMLS C4085211 Pain distress question C0004030 Aspergillosis HSDN C4085211 Pain distress question C0014008 Empty sella syndrome HSDN C0349588 Stature short C0220743 Childhood hypophosphatasia (disorder) MalaCards|HPO C1565249 Limitation, mobility C0011269 Dementia, vascular HSDN C1557397 Adverse event associated with pain C0020876 Ileal neoplasms HSDN C1557397 Adverse event associated with pain C0017924 Glycogen storage disease type v HSDN C1145670 Failure respiratory C0039263 Takayasu arteritis MalaCards C3539892 Pelvic pain in front C0002989 Epithelioid hemangioma of skin HSDN C4084724 Usual severity constipation C0027059 Myocarditis HSDN C1527344 Dysphonia C0242287 Isaacs syndrome HSDN C1557397 Adverse event associated with pain C0029899 Otosclerosis HSDN C4084725 Usual severity cough C0038940 Surgical wound dehiscence HSDN C0000727 Abdomen acute C0027051 Myocardial infarction HSDN C0011991 Loose stools C0235387 Porphyria type syndrome OrphaNet C4084788 Have dizziness C0037369 Smoking HSDN C1962972 Proteinuria adverse event C0000771 Abnormalities, drug induced HSDN C3539020 Pelvic pain decreasing in frequency C0020517 Hypersensitivity HSDN C3539889 Pelvic pain increasing in severity C0007860 Uterine cervicitis HSDN C0020455 Hypergammaglobulinemia C2674723 Ras-associated autoimmune leukoproliferative disorder MalaCards C0973461 Dysphasia C0079588 Ichthyosis, x-linked MalaCards C3539893 Pelvic pain occurs with intercourse C0041954 Ureteral diseases and syndromes HSDN C4084774 Have weight loss C0266209 Congenital dilatation of colon MalaCards C2911645 Weight loss adverse event C0024620 Primary malignant neoplasm of liver MalaCards C2096293 Ent surgical result ear vertigo C0007134 Renal cell carcinoma HSDN C1557397 Adverse event associated with pain C1262206 Iliotibial band syndrome HSDN C2984058 Have pain C1334928 Necrotic changes (finding) HSDN C2984058 Have pain C3203360 Suppuration HSDN C4084784 Diarrhea C0275524 Coinfection HSDN C1963087 Constipation adverse event C0004933 Behavior modification technique HSDN C0011991 Loose stools C0043046 Wasting syndrome HSDN C0022346 Yellow skin C0238339 Hereditary pancreatitis MalaCards|HSDN|HPO C4084776 Weight loss C1956346 Coronary artery disease HSDN C4084776 Weight loss C0018939 Hematological disease HSDN C0020458 Hyperhydrosis C0025221 Meleda disease OrphaNet|HPO C0151786 Weakness muscle C0014175 Endometriosis HSDN C1963087 Constipation adverse event C1839332 Rett syndrome, preserved speech variant HPO C0026838 Spasticity muscle C0009450 Disease caused by microorganism HSDN C0013395 Indigestion C0027809 Neurilemmoma HSDN C0042024 Urine incontinence C0014457 Eosinophilia HSDN C0026821 Cramp C0040053 Thrombosis HSDN C0476273 Distress respiratory C1855109 Methylmalonic aciduria cbla type HPO|UMLS C0006370 Bulimia C0085092 Parenting behavior HSDN C0587050 Lower extremity mass C0730193 Villonodular synovitis of lower limb UMLS C0424755 Fever symptoms C0035220 Respiratory distress syndrome, newborn HSDN C0030193 Sense of pain C0477379 Drug-induced headache, nec in snomedct UMLS C4085222 Nausea C2937358 Cerebral hemorrhage HSDN C1384666 Decreased hearing C0009395 Color perception HSDN C0018808 Murmur C0030567 Parkinson disease HSDN C0026961 Pupil dilated C0032001 Pituitary apoplexy MalaCards C0152116 Torticollis spasmodic C0410179 Scleroatonic muscular dystrophy MalaCards|HPO C0011168 Disorder deglutition C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C0028738 Nystagmus C2931008 Congenital disorder of glycosylation type 2a MalaCards C1962972 Proteinuria adverse event C0026936 Mycoplasma infections HSDN C0015672 Decreased energy C0038454 Cerebrovascular accident HSDN C0030554 Abnormal sensation C0039082 Syndrome HSDN C0018777 Deafness, conductive C0265251 Oto-palato-digital syndrome type 1 MalaCards C0002622 Amnesias C0041327 Tuberculosis, pulmonary HSDN C0518090 Frequency of pain question C0032372 Poliomyelitis, anterior, acute HSDN C0018989 Paresis of one side of body C1849722 Polyglucosan body disease, adult form OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C3711381 Hereditary diffuse leukoencephalopathy with spheroids UMLS C0522224 Palsied C1861329 Spinal canal stenosis HSDN C0042940 Disorder of voice C0003469 Anxiety disorders HSDN C0026838 Spasticity muscle C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0011127 Pressure ulcer HSDN C3898969 Have been vomiting C0037033 Necrotizing sialometaplasia HSDN C0004134 Dyssynergia C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO|UMLS C0151786 Weakness muscle C0543697 Mixed cryoglobulinemia OrphaNet|MalaCards C3665346 Loss sight C1846265 Microphthalmia, syndromic 2 MalaCards|HPO|UMLS C0020450 Hyperemesis gravidarum C0405075 Other preg.vomiting unspecif. UMLS C4084897 Sleep disturbance subordinate domain C0086647 Mucopolysaccharidosis type iiia MalaCards|HPO C4020887 Photodysphoria C1835897 Retinal cone dystrophy 3b MalaCards|HPO C0004134 Dyssynergia C0023448 Lymphoid leukemia HSDN C0029163 Hemorrhage mouth C0041296 Tuberculosis HSDN C4084725 Usual severity cough C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards C4084784 Diarrhea C0041234 Chagas disease OrphaNet|MalaCards C0018834 Brash C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C0424755 Fever symptoms C3536741 Discordant ventriculoarterial connection HSDN C1963091 Diarrhea adverse event C0015300 Exophthalmos HSDN C0017181 Gastrointestinal bleed C2931785 Juvenile dermatomyositis MalaCards C0000737 Abdomen pain C1335299 Pancreatic adenosquamous carcinoma UMLS C0005745 Blepharoptosis C0175703 Thrombocytopenia-absent radius syndrome MalaCards|HPO C0497247 Blood pressure elevation C3810324 Morbid obesity and spermatogenic failure MalaCards C2242996 Tingling C0268337 Ehlers-danlos syndrome, type 3 (disorder) HPO C1549543 Administration method - pain C0270327 Bedwetting HSDN C0018784 Deafness sensorineural C0162526 Aids-related opportunistic infections HSDN C1963184 Nystagmus adverse event C1859301 Cerebellar hypoplasia with endosteal sclerosis MalaCards C3665492 Pigmentations C0268425 Alstrom syndrome MalaCards C4084774 Have weight loss C0233629 Thinking and speaking disturbances HSDN C2984058 Have pain C0162835 Hypopigmentation disorder HSDN C0018777 Deafness, conductive C0206733 Strawberry nevus of skin HSDN C2919142 Short stature adverse event C0265312 Brachydactyly syndrome type e OrphaNet|HPO C1963184 Nystagmus adverse event C0268494 Oculocutaneous albinism type 1 MalaCards|HPO C0010520 Skin cyanosis C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards C0033790 Pseudobulbar palsy C0677866 Brain stem neoplasms HSDN C4084766 Vomiting C4085635 Appetite quality question HSDN C0005745 Blepharoptosis C3809233 Noonan syndrome 8 MalaCards C4085210 Usual severity pain C0027429 Nasal obstruction present finding HSDN C4085862 Bothered by nausea C0009062 Clostridia infection HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0349788 Arrhythmogenic right ventricular dysplasia HSDN C0005779 Clotting C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0557874 Global developmental delay C1853736 Congenital disorder of glycosylation, type iib MalaCards|HPO C1963281 Vomiting adverse event C0011303 Demyelinating diseases HSDN C4085211 Pain distress question C0024862 Masochism HSDN C0600142 Flash hot C0003467 Anxiety HSDN C0038990 Sweats C0022134 Islet cell adenoma MalaCards C0037317 Sleep disturbance C1392622 Chronic motor tics HPO C4084723 Constipation C0017075 Ganglioneuroma HSDN C0004604 Pain back C0001314 Acute disease HSDN C4084788 Have dizziness C1999266 Depression adverse event HSDN C3887873 Hearing loss C0019294 Hernia, inguinal HSDN C4084766 Vomiting C0029184 Orbital fracture HSDN C3541349 Syncope C0033923 Psychomotor function HSDN C0026826 High muscle tone C4014347 Pontocerebellar hypoplasia, type 10 MalaCards C0013421 Dystonia C0014055 Encephalitis, epidemic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242647 Mucosa-associated lymphoid tissue lymphoma HSDN C3641756 Have diarrhea C0006625 Cachexia HSDN C0151603 Edema generalized C0206624 Hepatoblastoma MalaCards C0034151 Hyperglobulinemic purpura C0023787 Lipodystrophy HSDN C0020649 Blood pressure decreased C1839780 Fragile x tremor/ataxia syndrome MalaCards|HPO C4085317 Diarrhea frequency C0008370 Cholestasis HSDN C0242936 Center pain C0033906 Psychological theories HSDN C2315100 Pediatric failure to thrive C1865373 Severe combined immunodeficiency, partial HPO C0162298 Stiffness joints C1956390 Cranial arteritis MalaCards C0042024 Urine incontinence C0011609 Drug eruptions HSDN C4084775 Usual severity weight loss C0012644 Animal disease models HSDN C0042024 Urine incontinence C0004623 Bacterial infections HSDN C4085661 Usual severity nausea C0021603 Sleep initiation and maintenance disorders HSDN C1963064 Anxiety adverse event C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C4084776 Weight loss C0271737 Addison's disease due to autoimmunity OrphaNet C3829611 Nausea frequency C0038356 Stomach neoplasms HSDN C0751401 Ophthalmoparesis C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C0019079 Bloody sputum C0746102 Chronic lung disease UMLS C0023380 Lethargy C0282193 Iron overload HSDN C3887784 Decreased urine output C0016724 Froehlich's syndrome HSDN C0587047 Mass of trunk C0342095 Breast hematoma UMLS C0018681 Headache, cephalalgia C0015347 Extinction HSDN C4085548 Usual severity dizziness C0034530 Injury radiation HSDN C0494475 Seizure generalized tonic clonic C0238111 Lennox-gastaut syndrome OrphaNet|HPO|MalaCards C2242996 Tingling C0018790 Cardiac arrest HSDN C4085317 Diarrhea frequency C1269683 Major depressive disorder HSDN C3146279 Coma C1859499 3-methylcrotonyl coa carboxylase 2 deficiency MalaCards C0004093 Asthenia C0006057 Botulisms HSDN C0018834 Brash C0175694 Smith-lemli-opitz syndrome OrphaNet|HPO|MalaCards C3815497 Cough C0270611 Brain damage HSDN C0039070 Collapse fleeting C0010054 Coronary arteriosclerosis HSDN|UMLS C0020796 Profoundly mentally retarded C3540845 Microphthalmia, isolated, with coloboma 8 MalaCards C0151908 Dry skin C3543867 Collodion fetus MalaCards C4084775 Usual severity weight loss C0011644 Scleroderma OrphaNet C0424755 Fever symptoms C0038454 Cerebrovascular accident HSDN C0007758 Cerebellar ataxia C3553264 Joubert syndrome 17 MalaCards C3665347 Vision impaired C2931789 Ausems wittebol-post hennekam syndrome OrphaNet|MalaCards C0033377 Caudal displacement C1852750 Coloboma, uveal, with cleft lip and palate and mental retardation HPO C0001825 Agraphia C0013537 Eclampsia HSDN C0014724 Burping C0038355 Diverticula stomach HSDN C0043094 Weight gain C0042384 Vasculitis HSDN C2048468 Inability to impregnate C1960540 Placental aromatase deficiency MalaCards C0017181 Gastrointestinal bleed C0034152 Henoch-schoenlein purpura MalaCards C4084769 Vomiting frequency C0004623 Bacterial infections HSDN C0042755 Virilisation C0030297 Pancreatic neoplasm HSDN C0035078 Failure kidney C1304205 Neutrophilic urticaria MalaCards C0518090 Frequency of pain question C2021655 Transvaginal ultrasound: anencephaly of fetus HSDN C0040264 Ear ringing sound C0242350 Erectile dysfunction HSDN C4084768 Usual severity vomiting C0268542 Ornithine carbamoyltransferase deficiency HSDN|HPO C1963137 Hydrocephalus adverse event C0410203 X-linked centronuclear myopathy HPO C1549543 Administration method - pain C0311389 Nonspecific urethritis HSDN C3887638 Failure to thrive in infant C2931246 Chromosome 17, trisomy 17p11 2 OrphaNet|HPO|MalaCards C0009806 Constipate C0149573 Structure of posterior inferior cerebellar artery HSDN C4084802 Usual severity diarrhea C0025268 Multiple endocrine neoplasia type 2a OrphaNet C1557397 Adverse event associated with pain C0311375 Arsenic poisoning HSDN C0011206 Delirium acute C0041755 Adverse reaction to drug HSDN C0557874 Global developmental delay C2931070 Schofer beetz bohl syndrome OrphaNet|MalaCards C0018524 Hallucinate C0205788 Histiocytoid hemangioma HSDN C0023012 Delay language C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO C1527344 Dysphonia C0032131 Plasmacytoma HSDN C3898969 Have been vomiting C0004030 Aspergillosis HSDN C0006370 Bulimia C3813607 Infantile gastroesophageal reflux HSDN C4084725 Usual severity cough C1258104 Diffuse scleroderma HSDN C2911645 Weight loss adverse event C0022658 Kidney diseases HSDN C0155552 Hearing loss mixed C1852502 Craniometaphyseal dysplasia, autosomal dominant HPO C0042963 Symptoms vomiting C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C0034933 Abnormal reflexes C0015423 Eyelid diseases HSDN C0003862 Pain joint C0032962 Pregnancy complications HSDN C0151786 Weakness muscle C1851801 Eds viib OrphaNet|HPO C0026838 Spasticity muscle C1857662 Coach syndrome MalaCards|HPO C0151786 Weakness muscle C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C1963170 Hypothermia adverse event C1864912 2-methylbutyryl-coa dehydrogenase deficiency HPO C1557397 Adverse event associated with pain C0242422 Parkinsonian disorders HSDN C0004134 Dyssynergia C1636667 Disorder characterized by eosinophilia HSDN C3539891 Pelvic pain to the rear C2911643 Encounter due to family history of osteoporosis HSDN C0018926 Emesis bloody C0812393 Cancer patients and suicide and depression HSDN C1856661 Cornea cloudy C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards|HPO C0812426 Kidney problem C0302810 Uremia syndrome UMLS C0018991 Paralysis one side of body C2364172 Adherence to medication regime HSDN C1963237 Insomnia adverse event C0040021 Thromboangiitis obliterans MalaCards C1145670 Failure respiratory C0010495 Cutis laxa MalaCards C1579931 Depressed - symptom C0268281 Infantile neuronal ceroid lipofuscinosis MalaCards|HPO C0039231 Heartbeats increased C0025427 Mercury poisoning OrphaNet|MalaCards C1963249 Tinnitus adverse event C0393807 Hereditary motor and sensory neuropathy with optic atrophy (disorder) HPO C4085548 Usual severity dizziness C0002395 Alzheimer's disease HSDN C4084769 Vomiting frequency C1135868 Gestational trophoblastic neoplasms HSDN C4084773 Bothered by weight gain C1956346 Coronary artery disease HSDN C3539022 Pelvic pain decreasing in severity C0314657 Genetic predisposition HSDN C1963281 Vomiting adverse event C0004933 Behavior modification technique HSDN C0018772 Deafness C3812171 Bradycardia by ecg finding HSDN C0085636 Light sensitivity C0006107 Concussion HSDN C0030193 Sense of pain C1706790 Peripheral ameloblastic carcinoma UMLS C0037316 Not enough sleeping C0008066 Child behavior disorders HSDN C1961131 Cough adverse event C0042138 Uterine neoplasms HSDN C0019214 Hepatosplenomegaly C1860157 Elejalde disease OrphaNet|MalaCards C1549543 Administration method - pain C1510502 Oxyphilic adenoma HSDN C3641756 Have diarrhea C0039981 Thoracic neoplasms HSDN C1838869 Proximal neurogenic muscle weakness C1832998 Epiphyseal dysplasia, multiple, 3 MalaCards|HPO C0003862 Pain joint C0085920 Brachial neuralgia MalaCards C2911647 Weight gain adverse event C0152156 Dystocia HSDN C4085317 Diarrhea frequency C0007784 Cerebral hemisphere hemorrhage HSDN C3641755 Have constipation C0342191 Familial dyshormonogenetic goiter MalaCards C2315100 Pediatric failure to thrive C1846142 Hoyeraal-hreidarsson syndrome OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0024228 Lymphatic diseases HSDN C1971624 Appetite absent C0271972 Thiamine-responsive megaloblastic anemia MalaCards C0024031 Back pain lower back C1962979 Burn adverse event HSDN C1384666 Decreased hearing C3501846 Noonan-like syndrome with loose anagen hair HPO C0557874 Global developmental delay C4015505 Spinocerebellar ataxia, autosomal recessive 18 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0033860 Psoriasis HSDN C0917816 Deficiency mental C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C3898969 Have been vomiting C2028283 History of premature birth HSDN C2203646 Jaundice C0024537 Malaria, vivax HSDN C1279888 Proteinuria of undiagnosed cause C3536715 Aa amyloidosis MalaCards C0600142 Flash hot C1384606 Dyspareunia HSDN C0575081 Abnormal gait C1858479 Spastic paraplegia 11, autosomal recessive OrphaNet|HPO|MalaCards C0007166 Cardiac output decreased C2963140 Arteriovenous fistula in use with two needles HSDN C0015672 Decreased energy C0021361 Female infertility HSDN C1963071 Back pain adverse event C0013473 Eating disorders HSDN C4085548 Usual severity dizziness C0025286 Meningioma HSDN C1963067 Atrial fibrillation adverse event C3697638 Familial short qt syndrome MalaCards C0020672 Body temperature decreased C0022658 Kidney diseases HSDN C0013421 Dystonia C1864840 Combined oxidative phosphorylation deficiency 3 MalaCards|HPO C0917816 Deficiency mental C0268496 Kramer syndrome OrphaNet|MalaCards C2984058 Have pain C0009953 Convulsive therapy HSDN C3887638 Failure to thrive in infant C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0344434 Atrial fibrillation ecg C1858725 Noncompaction of left ventricular myocardium, familial isolated, autosomal dominant 1 HPO C0027497 Queasy C1332246 Ampulla of vater clear cell adenocarcinoma UMLS C0152459 Striae C0017662 Glomerulonephritis, membranoproliferative HSDN C0015672 Decreased energy C1962983 Cataract adverse event HSDN C0018681 Headache, cephalalgia C0085605 Liver failure HSDN C2242996 Tingling C0021368 Inflammation HSDN C0349506 Sun sensitivity C1306229 Dyschromatosis universalis OrphaNet|HPO|MalaCards C0027066 Myoclonic jerking C0025063 Mediastinal neoplasms HSDN C4084726 Distress cough C0007453 Cattle disease HSDN C0015672 Decreased energy C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C4084767 Bothered by vomiting C0162532 Variegate porphyria MalaCards|HPO C4084784 Diarrhea C0020615 Hypoglycemia HSDN C0577567 Mass of urogenital structure C0269220 Cyst vulva UMLS C0426579 Anorexia symptom C0997768 Glaucoma HSDN C4084774 Have weight loss C0235974 Pancreatic carcinoma MalaCards C0522224 Palsied C0993582 Arthritis, experimental HSDN C0022346 Yellow skin C0017551 Gilbert disease (disorder) MalaCards C1963170 Hypothermia adverse event C0002874 Aplastic anemia HSDN C0013604 Edematous C0002874 Aplastic anemia HSDN C0013362 Dysarthrias C1850386 Giant axonal neuropathy 1 HPO C0234132 Pyramidal sign C1833296 Frontotemporal dementia, chromosome 3-linked UMLS C1963091 Diarrhea adverse event C1844663 Islets of langerhans, absence of HPO C0557874 Global developmental delay C0795851 14 trisomy mosaicism syndrome OrphaNet|MalaCards C0851578 Disorder sleep C0038644 Sudden infant death syndrome HSDN C2919142 Short stature adverse event C1857339 Deafness, congenital, with vitiligo and achalasia MalaCards C4085210 Usual severity pain C0032131 Plasmacytoma HSDN C1557397 Adverse event associated with pain C0035579 Rickets HSDN C0042963 Symptoms vomiting C1960459 Hereditary angioedema with normal c1 esterase inhibitor activity MalaCards C4042891 Sleep wake disorders C0243026 Sepsis HSDN C3539896 Pelvic pain occurs with urination C0019294 Hernia, inguinal HSDN C2984058 Have pain C0001163 Vestibulocochlear nerve diseases HSDN C4084802 Usual severity diarrhea C0007784 Cerebral hemisphere hemorrhage HSDN C4084774 Have weight loss C0014170 Endometrial neoplasms HSDN C3274924 Have been coughing C0796561 Melanoma vaccines HSDN C0595939 Stillborn C1856016 Hydrolethalus syndrome 1 HPO C2911645 Weight loss adverse event C0015726 Focused anxiety HSDN C3887873 Hearing loss C0035920 Rubella HSDN C1963093 Dizziness adverse event C0007131 Non-small cell lung carcinoma HSDN C0013404 Respiratory difficulty C0002949 Aneurysm, dissecting HSDN C3541349 Syncope C1999266 Depression adverse event HSDN C0263540 Nail loss C4014722 Sting-associated vasculopathy, infantile-onset MalaCards|UMLS C0004604 Pain back C0025149 Medulloblastoma MalaCards C0002963 Angina variant C0023903 Liver neoplasms HSDN C0007758 Cerebellar ataxia C0006109 Brain damage, chronic HSDN C4084775 Usual severity weight loss C0031345 Pharyngeal diseases HSDN C0030552 Paralysis partial C1856401 Etfa deficiencies HPO C1963091 Diarrhea adverse event C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C0014544 Epilepsy HSDN C2984057 Have nausea C0029443 Osteomyelitis HSDN C0010520 Skin cyanosis C0021449 Abuse inhalant HSDN C2237041 Shox gene with short stature C1834928 Cloverleaf skull micromelia thoracic dysplasia OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0027643 Neoplasm recurrence, local HSDN C0015672 Decreased energy C2347126 Microscopic polyarteritis HSDN C4085661 Usual severity nausea C0038160 Staphylococcal infections HSDN C0231218 Malaise generalized C3273126 Extrahepatic bile duct adenocarcinoma, biliary type UMLS C0036572 Convulsion C4014708 Hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies MalaCards|UMLS C3898969 Have been vomiting C1705810 Generic role HSDN C0013404 Respiratory difficulty C0000786 Spontaneous abortion HSDN C1963063 Anorexia adverse event C0153460 Malignant neoplasm of tail of pancreas MalaCards C0026821 Cramp C0009081 Congenital clubfoot HSDN C0002622 Amnesias C0008066 Child behavior disorders HSDN C3641755 Have constipation C0079487 Helicobacter infections HSDN C0557874 Global developmental delay C1860224 Ablepharon-macrostomia syndrome OrphaNet|HPO|MalaCards C0018772 Deafness C0026266 Mitral valve insufficiency HSDN C0011991 Loose stools C0011880 Diabetic ketoacidosis HSDN C0221151 Vomit projectile C0038354 Stomach diseases UMLS C2187990 Unable to perform sex C0268386 Amyloid polyneuropathy, swiss type MalaCards C0030554 Abnormal sensation C0042485 Venous insufficiency HSDN C1557397 Adverse event associated with pain C1547046 Kind of quantity - taste HSDN C3665492 Pigmentations C0030297 Pancreatic neoplasm MalaCards C0023014 Developmental disorder language C0597109 Nurse's role HSDN C4084802 Usual severity diarrhea C0039446 Telangiectasis HSDN C0542476 Forgetful C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C0013604 Edematous C2051831 Pectus excavatum HSDN C0002170 Alopecia disorders C0026948 Mycosis fungoides MalaCards C0349588 Stature short C0265253 Stickler syndrome (disorder) MalaCards C0518090 Frequency of pain question C0037221 Situs inversus HSDN C0040822 D tremors C0018916 Hemangioma HSDN C0026838 Spasticity muscle C2677299 Cerebroretinal microangiopathy with calcifications and cysts (disorder) HPO|UMLS C0042571 Vertigo subjective C0020538 Hypertensive disease HSDN C4084774 Have weight loss C0021845 Intestinal perforation HSDN C1963065 Apnea adverse event C0004096 Asthma HSDN C1963071 Back pain adverse event C0001122 Acidosis HSDN C0557874 Global developmental delay C1856057 Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type HPO C1962956 Flatulence adverse event C0025160 Megacolon HSDN C0018520 Breath odor C0004936 Mental disorders HSDN C2984057 Have nausea C0004623 Bacterial infections HSDN C0042571 Vertigo subjective C0022408 Arthropathy HSDN C4085211 Pain distress question C0026916 Mycobacterium avium-intracellulare infection HSDN C0877484 Soreness corner mouth C0221237 Angular cheilitis UMLS C0240715 Perineal lump C1274820 Penile sclerosing lipogranuloma UMLS C0231807 Dyspnea exertional C3554599 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 MalaCards|UMLS C0004941 Behavioral symptoms C1846707 Spinocerebellar ataxia 17 OrphaNet|HPO|MalaCards C0026821 Cramp C1846672 Muscular dystrophy, limb-girdle, type 2i MalaCards|HPO|UMLS C4084767 Bothered by vomiting C2711266 Infection by anisakis larva HSDN C1557397 Adverse event associated with pain C0376527 Neoplasm, skull base HSDN C1963071 Back pain adverse event C0014236 Endophthalmitis HSDN C0745924 Lower extremity tender C0007642 Cellulitis nos UMLS C0020505 Excessive eating C0006434 Burn injury HSDN C1279888 Proteinuria of undiagnosed cause C0023806 Lipomucopolysaccharidosis HPO C0424755 Fever symptoms C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0013395 Indigestion C0022665 Kidney neoplasm HSDN C0003910 Articulation disorder C0002736 Amyotrophic lateral sclerosis HSDN C0018524 Hallucinate C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0221263 Cafe au lait spot C3469528 Fanconi anemia, complementation group l MalaCards C0024032 Birth weight subnormal C1276035 Pena-shokeir syndrome type i MalaCards|HPO C0009676 Confusion state C0038525 Subarachnoid hemorrhage HSDN C4085210 Usual severity pain C0039786 Therapeutic communities HSDN C2984058 Have pain C0024143 Lupus nephritis HSDN C0018784 Deafness sensorineural C0014852 Esophageal diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0085278 Antiphospholipid syndrome HSDN C1549543 Administration method - pain C0042258 Vaginal neoplasms HSDN C1963071 Back pain adverse event C0042109 Urticaria HSDN C0003811 Cardiac rhythm disturbance C0013264 Muscular dystrophy, duchenne HPO C2984058 Have pain C0751795 Head injury penetrating HSDN C0015970 Fever unknown origin C0023269 Leiomyosarcoma HSDN C0349588 Stature short C2936831 10q partial trisomy OrphaNet|MalaCards C0018965 Blood urine C1857342 Deafness, cochlear, with myopia and intellectual impairment HPO C0043094 Weight gain C0014175 Endometriosis HSDN C0577567 Mass of urogenital structure C0268800 Simple renal cyst UMLS C0030486 Extremity paralysis, lower C0023281 Leishmaniasis HSDN C1963281 Vomiting adverse event C0037929 Spinal cord injuries HSDN C0036572 Convulsion C0751124 Epilepsy, absence, atypical UMLS C4084725 Usual severity cough C1720777 Functional laterality HSDN C0349588 Stature short C2931286 Mosaic variegated aneuplody microcephaly syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C0473586 Michelin tire baby syndrome MalaCards|HPO C0041105 Jaw spasm C0015459 Face injury HSDN C0030193 Sense of pain C0015414 Eye neoplasms HSDN C0860603 Anxiety symptom C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0028738 Nystagmus C0013581 Ectopia lentis MalaCards|HPO C4085549 Dizziness C0022658 Kidney diseases HSDN C0042024 Urine incontinence C0029456 Osteoporosis HSDN C0020450 Hyperemesis gravidarum C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0013604 Edematous C0349426 Ferrochelatase deficiency HPO C0086565 Liver function abnormal C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C0242936 Center pain C0020951 Immune complex diseases HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0279626 Squamous cell carcinoma of esophagus OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0016522 Foramen ovale, patent HSDN C4084766 Vomiting C0013364 Dysautonomia, familial HPO C2984058 Have pain C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C3665347 Vision impaired C2931753 Achromatopsia incomplete, x-linked MalaCards|HPO C3274924 Have been coughing C0018799 Heart diseases HSDN C0036572 Convulsion C0848377 Trauma to the abdomen HSDN C0030200 Intractable pain C0001418 Adenocarcinoma HSDN C4085222 Nausea C0524909 Hepatitis b, chronic MalaCards|HSDN C0042571 Vertigo subjective C1735340 Multifocal ventricular extrasystoles MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0022882 Infection laboratory HSDN C1557397 Adverse event associated with pain C0238015 Autonomic dysreflexia HSDN C4085210 Usual severity pain C0019034 Hemoglobin sc disease MalaCards|HSDN C4020887 Photodysphoria C0268495 Oculocutaneous albinism type 2 OrphaNet|HPO|MalaCards C0015469 Facial paralysis C0585442 Osteosarcoma of bone HSDN C0030975 Disorders perception C0020550 Hyperthyroidism HSDN C0041105 Jaw spasm C0035624 Mortis rigor HSDN C4084725 Usual severity cough C0019069 Hemophilia a HSDN C1145670 Failure respiratory C0265274 Achondrogenesis, type ib (disorder) HPO C0036572 Convulsion C0553754 Fit (in known epileptic) nos UMLS C0034155 Thrombotic thrombocytopenic purpura C0024299 Lymphoma HSDN C4085549 Dizziness C0025286 Meningioma HSDN C0036572 Convulsion C4225337 Epileptic encephalopathy, early infantile, 33 UMLS C0042025 Urinary incontinence stress C0860603 Anxiety symptoms HSDN C0037763 Spasm C0023418 Leukemia HSDN C4084725 Usual severity cough C1136033 Cutaneous mastocytosis MalaCards C3539020 Pelvic pain decreasing in frequency C0007860 Uterine cervicitis HSDN C4084766 Vomiting C0282333 Relaxation therapies HSDN C2203646 Jaundice C0039614 Tetanus HSDN C0850758 Pain pelvic C0037397 Behavior social HSDN C0349588 Stature short C1866495 Bartter syndrome, antenatal type 1 HPO C2237041 Shox gene with short stature C1865695 Spondylometaphyseal dysplasia, axial OrphaNet|MalaCards C0812426 Kidney problem C0085697 Chronic pyelonephritis UMLS C0026838 Spasticity muscle C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0497406 Over weight C0000768 Congenital abnormality HSDN C0030552 Paralysis partial C0026764 Multiple myeloma HSDN C0030193 Sense of pain C0016059 Fibrosis HSDN C0030486 Extremity paralysis, lower C0038525 Subarachnoid hemorrhage HSDN C0003862 Pain joint C0024145 Chilblain lupus 1 HPO C2203646 Jaundice C0002875 Cooley's anemia OrphaNet|HPO C1557397 Adverse event associated with pain C0006109 Brain damage, chronic HSDN C1963063 Anorexia adverse event C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C2024878 Cardiovascular surgery result: dyspnea C0003838 Arterial occlusive diseases HSDN C0033774 Skin pruritus C0302148 Blood clot HSDN C0004604 Pain back C0007134 Renal cell carcinoma HSDN C0015469 Facial paralysis C0035801 Diseases rodent HSDN C0015468 Face pain C0005491 Biofeedback HSDN C0036572 Convulsion C4078861 Non ketotic hyperglycinemia syndrome MalaCards C0018784 Deafness sensorineural C0079631 Interdisciplinary communication HSDN C3274924 Have been coughing C0238990 Acute lower respiratory tract infection MalaCards C2984058 Have pain C0041312 Tuberculosis git nos HSDN C0036396 Sciatica C0477611 Spin osteochondrosis, unsp HSDN C0023012 Delay language C0432442 Chromosome 18p deletion syndrome MalaCards C0019825 Voice hoarseness C0334405 Well differentiated ovarian sertoli-leydig cell tumor UMLS C0162835 Hypopigmentation C0334082 Nevus, epidermal (disorder) OrphaNet C0042755 Virilisation C0001206 Acromegaly HSDN C4085317 Diarrhea frequency C0040954 Infection by trichuris trichiura DiseaseOntology|MalaCards C0242936 Center pain C0031350 Pharyngitis HSDN C0019079 Bloody sputum C1332463 Basaloid large cell lung carcinoma UMLS C2919142 Short stature adverse event C3537440 Cystinosis, infantile nephropathic MalaCards C0277959 Hair coarseness C0028326 Noonan syndrome OrphaNet|HPO|MalaCards C4085549 Dizziness C0004623 Bacterial infections HSDN C0018784 Deafness sensorineural C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C4085211 Pain distress question C0029440 Osteoma HSDN C0013404 Respiratory difficulty C1306759 Eosinophilic disorder HSDN C4084784 Diarrhea C0007120 Bronchioloalveolar adenocarcinoma HSDN C3887638 Failure to thrive in infant C0037279 Skin diseases, metabolic HSDN C0151908 Dry skin C0796055 Mercaptolactate-cysteine disulfiduria OrphaNet|MalaCards C2911645 Weight loss adverse event C0017155 Gastritis, hypertrophic HSDN C0026838 Spasticity muscle C3808397 Cortical dysplasia, complex, with other brain malformations 1 MalaCards|UMLS C0004941 Behavioral symptoms C0282492 Sneddon syndrome OrphaNet|HPO|MalaCards C0016708 Micturition frequency and polyuria C0810038 Genitourinary symptoms and ill-defined conditions UMLS C0424755 Fever symptoms C1855652 Fetus small for gestational age HSDN C0033377 Caudal displacement C2931394 Katsantoni papadakou lagoyanni syndrome OrphaNet|MalaCards C4085210 Usual severity pain C1258666 Myxoid cyst HSDN C0241210 Speaking delay C2749022 Chromosome xp11.23-p11.22 duplication syndrome OrphaNet|HPO|MalaCards C0027497 Queasy C0011570 Mental depression HSDN C2315100 Pediatric failure to thrive C0020676 Hypothyroidism HSDN C0005745 Blepharoptosis C1837092 Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency HPO C0237326 Defecation pain C1836437 B-cell immunodeficiency, distal limb anomalies, and urogenital malformations MalaCards C1549543 Administration method - pain C0019151 Hepatic encephalopathy HSDN C0000737 Abdomen pain C1333308 Carcinoma of distal biliary tract UMLS C3829611 Nausea frequency C0010823 Cytomegalovirus infections HSDN C0016382 Cutaneous vascular engorgement C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0424755 Fever symptoms C0017181 Gastrointestinal hemorrhage HSDN C0036572 Convulsion C0032578 Polyploidy HSDN C0018784 Deafness sensorineural C1832215 Athabaskan brainstem dysgenesis MalaCards|HPO C0000737 Abdomen pain C0162316 Iron deficiency anemia HSDN C0007758 Cerebellar ataxia C0162532 Variegate porphyria HSDN C0851578 Disorder sleep C0024115 Lung diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0042932 Animal vocalizations HSDN C4084769 Vomiting frequency C2706915 Language:-:point in time:^patient:- HSDN C1397014 Imbalance C4225158 Spinocerebellar ataxia 41 UMLS C2364111 Gustatory anesthesia C0021645 Coma insulin HSDN C2237041 Shox gene with short stature C1859312 Camfak syndrome OrphaNet|HPO C0018681 Headache, cephalalgia C0007453 Cattle disease HSDN C1963237 Insomnia adverse event C3150674 Chromosome 15q24 deletion syndrome MalaCards C0040822 D tremors C0264797 Dilated cardiomyopathy secondary to viral myocarditis UMLS C0151889 Reflexes tendon increased C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C0037384 Snore C3891556 Chromosome xq26.3 duplication syndrome MalaCards|UMLS C0413252 Hypothermia due to exposure C1704436 Peripheral arterial diseases HSDN C4025811 Anemic pallor C0015625 Fanconi anemia MalaCards|HPO C0023015 Language handicap C1510586 Autism spectrum disorders HSDN C0002622 Amnesias C1556061 Electric injuries HSDN C3463815 Feel fatigue C0037275 Skin diseases, vesiculobullous HSDN C0020672 Body temperature decreased C0010308 Congenital hypothyroidism OrphaNet|MalaCards C4084784 Diarrhea C0024299 Lymphoma HSDN C2936821 Spinal cerebrospinal fluid leak C2937358 Cerebral hemorrhage HSDN C2315100 Pediatric failure to thrive C1257806 Chromosomal instability MalaCards C3463815 Feel fatigue C0038220 Status epilepticus HSDN C0017565 Gingiva hemorrhage C0877075 Intraosseous angioma MalaCards C0262527 Intermittent abdominal pain C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C0020615 Hypoglycemia nos C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C4085862 Bothered by nausea C0022951 Lactose intolerance HSDN C2096293 Ent surgical result ear vertigo C0043251 Wounds and injuries HSDN C0002963 Angina variant C0340464 Heartbeats ectopic HSDN C3670462 Pustular dermatitis C3875321 Inflammatory dermatosis UMLS C0015469 Facial paralysis C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards C2029884 Hearing loss by exam C0002895 Anemia, sickle cell HSDN C0028738 Nystagmus C1849437 Mainzer-saldino disease MalaCards|HPO C0270948 Neurogenic muscular atrophy C3810289 Spastic paraplegia 64, autosomal recessive MalaCards C0004604 Pain back C1707400 Classic medulloblastoma MalaCards C4085211 Pain distress question C0007279 Carotid body paraganglioma HSDN C0015672 Decreased energy C1334968 Nodular lymphocyte predominant hodgkin lymphoma MalaCards C3539896 Pelvic pain occurs with urination C0029400 Osteitis HSDN C0034124 Pupillary disorder C0004114 Astrocytoma HSDN C0042571 Vertigo subjective C0017612 Glaucoma, open-angle HSDN C0497247 Blood pressure elevation C1852456 Cryoglobulinemia, familial mixed MalaCards C4084773 Bothered by weight gain C0039685 Tetralogy of fallot HSDN C3898969 Have been vomiting C0026780 Mumps HSDN C0851578 Disorder sleep C0005283 Beta thalassemia HSDN C0155552 Hearing loss mixed C1550639 Specimen type - fistula HSDN C1263846 Attention deficit disorder with hyperactivity C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0007786 Brain ischemia HSDN C3146279 Coma C0878576 Posterior leucoencephalopathy syndrome HSDN C1963281 Vomiting adverse event C0001175 Acquired immunodeficiency syndrome HSDN C0235153 Sensory hallucination C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C4085211 Pain distress question C2240374 Eosinophil count raised HSDN C0020450 Hyperemesis gravidarum C0156694 Mild hyperemesis gravidarum, antepartum condition or complication UMLS C0042571 Vertigo subjective C1579931 Depressed - symptom HSDN C0019209 Large liver C0268151 Classical galactosemia MalaCards|HPO C0018772 Deafness C0021831 Intestinal diseases HSDN C0007758 Cerebellar ataxia C1412750 Bbs5 gene HPO C0004134 Dyssynergia C1834559 Continuous muscle fiber activity, hereditary OrphaNet|HPO C0151686 Growth retardation C3854181 Nevus sebaceous HPO C1557397 Adverse event associated with pain C0729346 Osteochondritis juvenilis HSDN C1963071 Back pain adverse event C0007873 Uterine cervical neoplasm HSDN C0241165 Skin thickening C1274216 Punctate palmoplantar keratoderma OrphaNet C4042891 Sleep wake disorders C0003811 Cardiac arrhythmia HSDN C0042963 Symptoms vomiting C1304456 Congo hemorrhagic fever MalaCards C0030552 Paralysis partial C3151853 Mcleod syndrome with chronic granulomatous disease HPO C0036572 Convulsion C0022578 Keratoconus HSDN C0015672 Decreased energy C0007820 Cerebrovascular disorders HSDN C0018808 Murmur C0039263 Takayasu arteritis HSDN C0018681 Headache, cephalalgia C0011119 Decompression sickness HSDN C1384666 Decreased hearing C0014859 Esophageal neoplasms HSDN C0424755 Fever symptoms C0027794 Neural tube defects HSDN C4084724 Usual severity constipation C0011570 Mental depression HSDN C4085862 Bothered by nausea C0032963 Pregnancy complications, cardiovascular HSDN C0031911 Pigment deposition C0546837 Malignant neoplasm of esophagus MalaCards C0231218 Malaise generalized C0018572 Hand, foot and mouth disease DiseaseOntology|MalaCards C0003811 Cardiac rhythm disturbance C1833607 Hydrocephalus, endocardial fibroelastosis, and cataracts OrphaNet|MalaCards C3887873 Hearing loss C0017653 Glomus tumor HSDN C0039070 Collapse fleeting C0043251 Wounds and injuries HSDN C0015300 Ocular proptosis C1847197 Vascular malformation, primary intraosseous MalaCards C4084769 Vomiting frequency C0020522 Delayed hypersensitivity HSDN C4085210 Usual severity pain C0030793 Pelvis tumor HSDN C3146279 Coma C0001175 Acquired immunodeficiency syndrome HSDN C0151686 Growth retardation C3711387 Autosomal recessive primary microcephaly OrphaNet C2073625 X-ray of chest: pleural effusion C0149521 Pancreatitis, chronic MalaCards C0150055 Pain chronic C0001624 Adrenal gland neoplasms HSDN C1384666 Decreased hearing C2931452 Hirschsprung disease, deafness and polydactyly MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0022367 Jaw, edentulous, partially HSDN C0013421 Dystonia C0001430 Adenoma HSDN C4084769 Vomiting frequency C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0375572 Abdominal rigidity, other specified site; multiple sites C0810319 Other and unspecified gastrointestinal disorders UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0010633 Cystadenoma HSDN C0221752 Rbc urine C0342749 Glycogen storage disease ic MalaCards|HPO C4084727 Cough frequency C0038436 Post-traumatic stress disorder HSDN C4084766 Vomiting C0029132 Disorder of the optic nerve HSDN C4085317 Diarrhea frequency C2984572 Malaria pathway HSDN C2237041 Shox gene with short stature C0026760 Multiple epiphyseal dysplasia OrphaNet|MalaCards C0015672 Decreased energy C0027804 Fatigue neurosis UMLS C0013604 Edematous C0008698 Maxillary sinusitis chronic HSDN C4085222 Nausea C0043124 West nile fever MalaCards C0011991 Loose stools C0042075 Urologic diseases HSDN C0557874 Global developmental delay C3280866 Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) MalaCards C0036572 Convulsion C1275084 Angioma hereditary neurocutaneous OrphaNet C0271215 Blindness legal C2677434 Orofacial cleft 11 MalaCards C1963093 Dizziness adverse event C0079487 Helicobacter infections HSDN C4085661 Usual severity nausea C0019285 Diaphragmatic hernia traumatic HSDN C0034933 Abnormal reflexes C0034882 Rectal diseases HSDN C4084784 Diarrhea C0349231 Phobic anxiety disorder HSDN C0233514 Behavior abnormal C3683846 Chromosome 17p deletion syndrome MalaCards C2029884 Hearing loss by exam C2937358 Cerebral hemorrhage HSDN C0009676 Confusion state C0007020 Carbon monoxide poisoning HSDN C1961131 Cough adverse event C0013080 Down syndrome HSDN C0012569 Double vision C0206255 Malaria vaccine HSDN C0518090 Frequency of pain question C0007279 Carotid body paraganglioma HSDN C0026603 Motion sickness C0027651 Tumor HSDN C2032396 Pelvic pain on the right C0206654 Leiomyomatosis HSDN C0152116 Torticollis spasmodic C0270969 Zebra body myopathy OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0023801 Lipomatosis HSDN C4085317 Diarrhea frequency C0007273 Carotid artery diseases HSDN C0042963 Symptoms vomiting C0004052 Aspiration of vomitus HSDN C3829611 Nausea frequency C0039483 Giant cell arteritis HSDN C0018991 Paralysis one side of body C0035243 Respiratory tract infections HSDN C0009421 Comatose C0038395 Streptococcal infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017075 Ganglioneuroma HSDN C3541349 Syncope C0011615 Dermatitis, atopic HSDN C1565249 Limitation, mobility C0038016 Spondylolisthesis HSDN C4085210 Usual severity pain C0020497 Cortical congenital hyperostosis HSDN C0035455 Rhinitis C0013575 Ectodermal dysplasia MalaCards C0085631 Abnormal excitement C0037646 Psychiatric somatic therapy HSDN C3274924 Have been coughing C3540844 Ciliary dyskinesia, primary, 20 MalaCards C0022346 Yellow skin C0037054 Sickle cell trait MalaCards C4084769 Vomiting frequency C0001721 Emotional affect HSDN C4084769 Vomiting frequency C0947622 Cholecystolithiasis HSDN C0023014 Developmental disorder language C0022758 Kap HSDN C2911645 Weight loss adverse event C0268080 Hypercalcemia, idiopathic, of infancy HPO C0857305 Thrombocytopenia purpura C0010346 Crohn disease HSDN C0221232 Welts C0413236 Acquired c1 esterase inhibitor deficiency UMLS C0018524 Hallucinate C0017152 Gastritis HSDN C3641756 Have diarrhea C0006663 Calcinosis HSDN C3665346 Loss sight C2020284 Stickler syndrome, type 1 MalaCards|HPO C0020672 Body temperature decreased C0005891 Bodies image HSDN C1963252 Tremor adverse event C1962963 Osteoporosis adverse event HSDN C0003862 Pain joint C0037286 Skin neoplasms HSDN C0232466 Feeding difficulty C3809216 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 MalaCards C0002962 Angina C0221391 Melanosis coli HSDN C1963066 Joint pain adverse event C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0003862 Pain joint C0037578 Soft tissue injury HSDN C1963249 Tinnitus adverse event C0151740 Intracranial hypertension HSDN C4084775 Usual severity weight loss C0037047 Sibling HSDN C0016199 Pain flank C0034065 Pulmonary embolism HSDN C0020458 Hyperhydrosis C0878675 Erdheim-chester disease OrphaNet|MalaCards C4084726 Distress cough C0038663 Suicide attempt HSDN C0013428 Painful urination C1519927 Vaginal non-keratinizing squamous cell carcinoma UMLS C0039070 Collapse fleeting C0004936 Mental disorders HSDN C0019825 Voice hoarseness C0010068 Coronary heart disease HSDN C0221263 Cafe au lait spot C0025267 Multiple endocrine neoplasia type 1 HSDN|HPO C0011991 Loose stools C0027022 Myeloproliferative disease HSDN C0151311 Cranial nerve palsy C0024454 Maffucci syndrome MalaCards|HPO C4084727 Cough frequency C1527407 Eosinophilic pneumonia DiseaseOntology C0024031 Back pain lower back C0034040 Puerperal disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0178324 Blood vessel injury HSDN C4085211 Pain distress question C0009187 Coccidiosis HSDN C0030552 Paralysis partial C0024534 Malaria, cerebral HSDN C1963071 Back pain adverse event C0018273 Growth disorders HSDN C0027497 Queasy C0020456 Hyperglycemia HSDN C2911645 Weight loss adverse event C0006840 Candidiasis HSDN C2364111 Gustatory anesthesia C0029888 Otitis media purulent HSDN C0023012 Delay language C1968552 Mental retardation, x-linked, with spasticity HPO C0518090 Frequency of pain question C0013537 Eclampsia HSDN C0312416 Morning sickness C0042134 Uterine hemorrhage HSDN C2984058 Have pain C0019285 Diaphragmatic hernia traumatic HSDN C3665347 Vision impaired C1863198 Albinism, ocular, with sensorineural deafness (disorder) HPO C0013404 Respiratory difficulty C0035229 Respiratory insufficiency UMLS C3814874 Loss of appetite question C0152945 Anthrax gastrointestinal MalaCards C0011991 Loose stools C0010074 Coronary vessel anomalies HSDN C4050613 Anxiety C0001529 Dercum disease OrphaNet|MalaCards C4084725 Usual severity cough C0023473 Myeloid leukemia, chronic HSDN C0030193 Sense of pain C0269099 Essential vulvodynia UMLS C0151686 Growth retardation C0265341 Rieger syndrome HPO C0853986 Lymphocytes decreased C0340834 Hennekam lymphangiectasia lymphedema syndrome MalaCards C2032395 Pelvic pain on the left C0040053 Thrombosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085315 Toxoplasmosis, cerebral HSDN C0018681 Headache, cephalalgia C0162637 Strongylida infections HSDN C0020458 Hyperhydrosis C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C3665492 Pigmentations C0334092 Hamartomatous polyp MalaCards C0023012 Delay language C0342803 Dihydropyrimidinase deficiency HPO C0027497 Queasy C0340629 Aortic aneurysm without mention of rupture nos HSDN C0349506 Sun sensitivity C3551173 Uv-sensitive syndrome 1 MalaCards C4085210 Usual severity pain C2267227 Bulimia nervosa HSDN C2984058 Have pain C0039240 Supraventricular tachycardia HSDN C0454644 Delayed language development C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C0015300 Ocular proptosis C1334698 Meningothelial cell neoplasm MalaCards C0018784 Deafness sensorineural C0035435 Rheumatism HSDN C3539891 Pelvic pain to the rear C0008519 Ectopic tissue HSDN C0003862 Pain joint C0221013 Mastocytosis, systemic MalaCards C3274924 Have been coughing C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C0036572 Convulsion C0393703 Myoclonic absence epilepsy UMLS C0557874 Global developmental delay C2931817 Chromosome 2q37 deletion syndrome OrphaNet|HPO|MalaCards C0042928 Paralysis vocal cord C4085311 Depression - recess HSDN C0015672 Decreased energy C0032229 Pleural neoplasms HSDN C0000731 Abdomen distention C0024620 Primary malignant neoplasm of liver MalaCards C0042755 Virilisation C0000786 Spontaneous abortion HSDN C0027497 Queasy C0040046 Thrombophlebitis HSDN C0019209 Large liver C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0151740 Intracranial hypertension HSDN C0518090 Frequency of pain question C0011405 Pulp disorder HSDN C0011991 Loose stools C0578159 Antibiotic-associated diarrhea UMLS C1963093 Dizziness adverse event C0014121 Bacterial endocarditis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030805 Bullous pemphigoid HSDN C0028738 Nystagmus C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C4084802 Usual severity diarrhea C0010674 Cystic fibrosis HSDN C4084725 Usual severity cough C0033036 Atrial premature complexes HSDN C0019825 Voice hoarseness C0018199 Granuloma, plasma cell HSDN C0917816 Deficiency mental C2674876 Loeys dietz syndrome, type 1b HPO C0038002 Spleen enlargement C0455988 Hydrops fetalis, non-immune MalaCards C0042571 Vertigo subjective C0020619 Hypogonadism HSDN C0010200 Cough symptom C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2024893 Cardiovascular surgery result: fatigue C1962963 Osteoporosis adverse event HSDN C4084725 Usual severity cough C1762616 Meningioma, benign, no icd-o subtype HSDN C0042514 Ventricular tachycardia C0340485 Familial ventricular tachycardia MalaCards C0011991 Loose stools C0006818 Campylobacter infection DiseaseOntology C0043094 Weight gain C0040185 Tibia fracture HSDN C0270948 Neurogenic muscular atrophy C1860808 Triosephosphate isomerase deficiency OrphaNet|HPO C0151908 Dry skin C1866504 Photosensitive trichothiodystrophy MalaCards|UMLS C0008031 Pain chest C0007786 Brain ischemia HSDN C0427055 Face weakness C0796274 Brown-vialetto-van laere syndrome OrphaNet|UMLS|HPO|MalaCards C0002962 Angina C0019360 Herpes zoster disease HSDN C0030486 Extremity paralysis, lower C0005586 Bipolar disorder HSDN C0020673 Hypothermia (central) (local) C0001125 Acidosis, lactic HSDN C0020455 Hypergammaglobulinemia C0038166 Staphylococcal skin infections HSDN C1963252 Tremor adverse event C0003864 Arthritis HSDN C0027498 Nausea vomiting C3469606 Pseudohypoaldosteronism, type iie MalaCards C0007398 Catatonic C1555865 Forensic psychiatry HSDN C4085548 Usual severity dizziness C0024630 Malingering HSDN C4084766 Vomiting C0026782 Mumps vaccine HSDN C0023012 Delay language C3665349 Secondary hypothyroidism OrphaNet|MalaCards C0424755 Fever symptoms C0018789 Cardiac aneurysm HSDN C2242996 Tingling C0023827 Liposarcoma MalaCards C0020458 Hyperhydrosis C0268360 Osteogenesis imperfecta, recessive perinatal lethal OrphaNet C0020649 Blood pressure decreased C1849813 Glycogen storage disease of heart, lethal congenital MalaCards|HPO C0018777 Deafness, conductive C0001418 Adenocarcinoma HSDN C0000727 Abdomen acute C0011882 Diabetic neuropathies HSDN C0036572 Convulsion C1527336 Sjogren's syndrome HSDN C0030975 Disorders perception C0751772 Rem sleep behavior disorder HSDN C4085210 Usual severity pain C0270857 Epilepsy, reflex HSDN C1000483 Genus anemia C0345407 Osteopetrosis, autosomal recessive 3 HPO C0030486 Extremity paralysis, lower C0007760 Cerebellar diseases HSDN C0042963 Symptoms vomiting C0036875 Disorders of sex development HSDN C0022346 Yellow skin C4225155 Anemia, sideroblastic, 3, pyridoxine-refractory UMLS C4085317 Diarrhea frequency C0034040 Puerperal disorders HSDN C4084766 Vomiting C0002871 Anemia HSDN C3641756 Have diarrhea C1865371 Severe combined immunodeficiency, athabaskan-type HPO C0019209 Large liver C0268146 Glucose-6-phosphate transport defect MalaCards|HPO C0413252 Hypothermia due to exposure C3489413 Lipomatosis, multiple HSDN C4084768 Usual severity vomiting C0022865 Obstetric labor complications HSDN C2024893 Cardiovascular surgery result: fatigue C0008313 Cholangitis, sclerosing HSDN C0042963 Symptoms vomiting C3812171 Bradycardia by ecg finding HSDN C0026821 Cramp C3495422 Finding relating to sexuality and sexual activity HSDN C0013456 Pain ear C0038994 Gustatory sweating HSDN C0085631 Abnormal excitement C1861513 Cluster headache, familial UMLS C0010520 Skin cyanosis C3163620 Hypotension adverse event HSDN C4084784 Diarrhea C0020459 Hyperinsulinism HSDN C0150055 Pain chronic C0035126 Reperfusion injury HSDN C0917816 Deficiency mental C4014864 Mental retardation, autosomal recessive 45 MalaCards C0015672 Decreased energy C0752287 Sleep disorders, intrinsic HSDN C3274920 Have shortness of breath question C0149725 Lower respiratory tract infection MalaCards C0022346 Yellow skin C0040136 Thyroid neoplasm HSDN C0027066 Myoclonic jerking C0039145 Syringomyelia and syringobulbia HSDN C4085210 Usual severity pain C0040820 Trematode infections HSDN C2242996 Tingling C0040028 Thrombocythemia, essential OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0151491 Congenital musculoskeletal anomalies HSDN C2919142 Short stature adverse event C1860145 Acrocraniofacial dysostosis OrphaNet|MalaCards C3641756 Have diarrhea C0013595 Eczema HSDN C2911647 Weight gain adverse event C3812171 Bradycardia by ecg finding HSDN C0917816 Deficiency mental C3698507 Porencephaly, post-traumatic MalaCards C0011991 Loose stools C0742909 Cryptococcal infection disseminated UMLS C1145670 Failure respiratory C0796176 Stuve-wiedemann syndrome HPO C0020615 Hypoglycemia nos C1415614 Hmgcl gene HPO C0042571 Vertigo subjective C0395920 Migrainous vertigo UMLS C2315100 Pediatric failure to thrive C0268130 Hereditary orotic aciduria, type 1 MalaCards C4085548 Usual severity dizziness C1412004 Tumor of the pineal region HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007762 Cerebellar neoplasms HSDN C4085317 Diarrhea frequency C1705714 Lats1 wt allele HSDN C0413252 Hypothermia due to exposure C0031511 Pheochromocytoma HSDN C0004134 Dyssynergia C0024814 Marinesco-sjogren syndrome MalaCards C0263629 Tumor-like lesions of the skin C0333988 Hyperplasia pseudoepitheliomatous UMLS C0557874 Global developmental delay C0282577 Congenital disorders of glycosylation OrphaNet|MalaCards C1963281 Vomiting adverse event C0556346 Binge drinking HSDN C4085642 Level of joint stiffness C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0242936 Center pain C0039504 Injuries tendon HSDN C2984057 Have nausea C0795623 Hepatitis a vaccine, inactivated HSDN C0751837 Gait ataxic C0006112 Brain diseases, metabolic HSDN C1268593 Metabolic presbycusis C0033074 Presbycusis UMLS C0424755 Fever symptoms C0010481 Cushing syndrome HSDN C1549543 Administration method - pain C0005416 Biliary dyskinesia HSDN C2032396 Pelvic pain on the right C0037369 Smoking HSDN C3539896 Pelvic pain occurs with urination C3178770 Nutcracker syndrome, renal HSDN C0700078 Deep tendon reflex decrease C0268138 Xeroderma pigmentosum, complementation group d HPO C0015672 Decreased energy C1366535 Avp gene HSDN C0041657 Consciousness loss C2239176 Liver carcinoma HSDN C0232493 Epigastric pain C0743583 Esophageal reflux dyspepsia UMLS C4085549 Dizziness C0033941 Psychoses, substance-induced HSDN C1962972 Proteinuria adverse event C0027092 Myopia HSDN C3887873 Hearing loss C0700327 Clinical findings relating to memory HSDN C0018524 Hallucinate C0751757 Hypersomnolence, idiopathic HSDN C0015672 Decreased energy C0267797 Acute hepatitis UMLS C0038506 Stutter C0017510 Gestures HSDN C1963086 Confusion adverse event C0012746 Dissociative disorder HSDN C1860844 Sparse, thin hair C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C4084776 Weight loss C0022116 Ischemia HSDN C0013421 Dystonia C0743332 Focal dystonia UMLS C3539890 Pelvic pain causes awakening at night C0684743 Malignant neoplasm of muscle HSDN C0018772 Deafness C0024117 Chronic obstructive airway disease HSDN C0033774 Skin pruritus C1865643 Cholestasis, progressive familial intrahepatic 3 HPO|UMLS C0162298 Stiffness joints C0220722 Cerebrooculofacioskeletal syndrome 1 OrphaNet|HPO C0016382 Cutaneous vascular engorgement C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C0349588 Stature short C1834759 Momo syndrome MalaCards C0033377 Caudal displacement C4012727 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 MalaCards C0004310 Auditory disorder process C0036939 Shared paranoid disorder HSDN C4084724 Usual severity constipation C0037369 Smoking HSDN C0004134 Dyssynergia C0221036 Acrodermatitis enteropathica HPO C0016382 Cutaneous vascular engorgement C0149931 Migraine disorders HSDN C0037315 Breathing disorder during sleeping C0342853 Sialuria OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0009450 Disease caused by microorganism HSDN C0152169 Colic renal C0003496 Aortic rupture HSDN C4084802 Usual severity diarrhea C0040588 Tracheoesophageal fistula HSDN C0032617 High urine output C0030521 Parathyroid neoplasms HSDN C0018991 Paralysis one side of body C1955869 Malformations of cortical development HSDN C4085641 Level of joint pain C0033788 Pseudo-hurler polydystrophy MalaCards C0878773 Bladder hyperactive C0234421 Conscious HSDN C4042891 Sleep wake disorders C0011881 Diabetic nephropathy HSDN C0030486 Extremity paralysis, lower C0024115 Lung diseases HSDN C4084724 Usual severity constipation C0008925 Cleft palate HSDN C4085210 Usual severity pain C0221391 Melanosis coli HSDN C0518090 Frequency of pain question C0027343 Toenail ingrown HSDN C0557874 Global developmental delay C2931515 Piussan lenaerts mathieu syndrome MalaCards C1963093 Dizziness adverse event C0236736 Cocaine-related disorders HSDN C0013604 Edematous C1963090 Dehydration adverse event HSDN C0424755 Fever symptoms C1527258 Infantile paralysis MalaCards C0004604 Pain back C0406608 Pelvic lipomatosis UMLS C3146279 Coma C0019360 Herpes zoster disease HSDN C0151825 Ostalgia C2931189 Neural crest tumor MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C2021655 Transvaginal ultrasound: anencephaly of fetus HSDN C1963281 Vomiting adverse event C0037397 Behavior social HSDN C0013421 Dystonia C0162666 Mitochondrial encephalomyopathies HSDN C0018772 Deafness C0008096 Children exceptional HSDN C0001707 Aerophagia C0035372 Rett syndrome HSDN C3203358 Alveolar hypoventilation C0014548 Epilepsy, generalized HSDN C0009080 Finger clubbing C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0557874 Global developmental delay C0795845 Chromosome 12, 12p trisomy OrphaNet|MalaCards C0085593 Chill C0571311 Quinine allergy UMLS C4084773 Bothered by weight gain C0011603 Dermatitis HSDN C4085549 Dizziness C0017181 Gastrointestinal hemorrhage HSDN C2911645 Weight loss adverse event C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C1145670 Failure respiratory C0265251 Oto-palato-digital syndrome type 1 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2937421 Prostatic hyperplasia HSDN C4084802 Usual severity diarrhea C0028796 Dermatitis, occupational HSDN C0221263 Cafe au lait spot C0751774 Nocturnal myoclonus syndrome HSDN C0013362 Dysarthrias C0796092 Oculo-cerebro-cutaneous syndrome MalaCards C0003862 Pain joint C0585274 Periodic syndrome OrphaNet|HPO C3146279 Coma C0037397 Behavior social HSDN C3539890 Pelvic pain causes awakening at night C3244301 Coverage level - family HSDN C2984058 Have pain C0042162 Uveal neoplasms HSDN C0018784 Deafness sensorineural C0010346 Crohn disease HSDN C0030193 Sense of pain C0020640 Inherited factor ii deficiency HSDN C0026821 Cramp C0027121 Myositis HSDN C0036572 Convulsion C0022729 Klebsiella infections HSDN C4084788 Have dizziness C0037019 Shy-drager syndrome HSDN C0024031 Back pain lower back C0812393 Cancer patients and suicide and depression HSDN C0020672 Body temperature decreased C0020461 Hyperkalemia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0025229 Melioidosis DiseaseOntology|MalaCards C4084776 Weight loss C0037356 Smallpox virus HSDN C2237041 Shox gene with short stature C1850168 Bruck syndrome 1 OrphaNet|HPO|MalaCards C4085211 Pain distress question C3160917 Bladder pain syndrome OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0023055 Laryngeal neoplasm HSDN C0595939 Stillborn C1848599 Vacterl association with hydrocephalus HPO C0015300 Ocular proptosis C3280215 Holoprosencephaly 11 MalaCards C3898969 Have been vomiting C0011603 Dermatitis HSDN C4084784 Diarrhea C0029443 Osteomyelitis HSDN C0005745 Blepharoptosis C0265301 Sclerosteosis OrphaNet|HPO|MalaCards C0455880 Urinary stream decreased force C0152032 Hesitancy urination UMLS C2911645 Weight loss adverse event C0014511 Epithelial cyst HSDN C1962972 Proteinuria adverse event C1963137 Hydrocephalus adverse event HSDN C1963087 Constipation adverse event C0393911 Pure autonomic failure MalaCards C0030486 Extremity paralysis, lower C0028768 Obsessive-compulsive disorder HSDN C0043094 Weight gain C0036202 Sarcoidosis HSDN C0031911 Pigment deposition C0042170 Uveomeningoencephalitic syndrome MalaCards C1963184 Nystagmus adverse event C1845069 Albinism, ocular, with late-onset sensorineural deafness (disorder) OrphaNet C0476232 Jaundice, unspecified, not of newborn C0810314 Other and unspecified liver disorders UMLS C0015469 Facial paralysis C2931107 Myasthenic syndrome, congenital, postsynaptic slow-channel MalaCards C0020305 Fetal edema C1865270 Bartter syndrome, type 4a HPO C4084766 Vomiting C0042514 Tachycardia, ventricular HSDN C4084766 Vomiting C0023890 Liver cirrhosis HSDN C1549543 Administration method - pain C0024440 Macular edema, cystoid HSDN C0518090 Frequency of pain question C0004245 Atrioventricular block HSDN C2024878 Cardiovascular surgery result: dyspnea C0697038 Asclepias tuberosa HSDN C0003469 Anxiety disorder C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C4084769 Vomiting frequency C0023066 Laryngismus HSDN C0016199 Pain flank C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C1838869 Proximal neurogenic muscle weakness C2750536 Nemaline myopathy 3, with intranuclear rods HPO C4085317 Diarrhea frequency C0267662 Congenital chloride diarrhea MalaCards|HPO C4085222 Nausea C0031511 Pheochromocytoma MalaCards C0040264 Ear ringing sound C2911643 Encounter due to family history of osteoporosis HSDN C4084788 Have dizziness C0011849 Diabetes mellitus HSDN C4020887 Photodysphoria C2931258 Amaurosis congenita of leber, type 1 MalaCards|HPO C0008031 Pain chest C0040034 Thrombocytopenia HSDN|UMLS C4085210 Usual severity pain C0024314 Lymphoproliferative disorders HSDN C0152116 Torticollis spasmodic C1851945 Dystonia 1, torsion, autosomal dominant HPO C3641755 Have constipation C1563706 Nephrogenic diabetes insipidus, type ii HPO C0036572 Convulsion C0036323 Schistosomiasis HSDN C3539892 Pelvic pain in front C0007097 Carcinomas HSDN C3887873 Hearing loss C0018916 Hemangioma HSDN C0242936 Center pain C0032460 Polycystic ovary syndrome HSDN C3539892 Pelvic pain in front C0023903 Liver neoplasms HSDN C4084727 Cough frequency C0011334 Dental caries HSDN C4084776 Weight loss C0026590 Child mother relationship HSDN C4084802 Usual severity diarrhea C0040558 Toxoplasmosis HSDN C0413252 Hypothermia due to exposure C0041022 Pulmonary valve, stenosis, with patent foramen ovale HSDN C1961131 Cough adverse event C0033860 Psoriasis HSDN C0013395 Indigestion C0032285 Pneumonia HSDN C4084723 Constipation C0018934 Hematocolpos HSDN C0241165 Skin thickening C0032027 Pityriasis rubra pilaris OrphaNet|MalaCards C4084774 Have weight loss C0206702 Klatskin tumor MalaCards C0040822 D tremors C1854336 Paragangliomas 3 MalaCards C0016382 Cutaneous vascular engorgement C0017150 Gastrinoma MalaCards C0028738 Nystagmus C1846980 Senior-loken syndrome 3 MalaCards C0040460 Dental pain C4084909 Depression subordinate domain HSDN C0020672 Body temperature decreased C0546884 Hypovolemia HSDN C4084723 Constipation C0007873 Uterine cervical neoplasm HSDN C0522224 Palsied C0013295 Duodenal ulcer HSDN C0013604 Edematous C0011127 Pressure ulcer HSDN C0026821 Cramp C0004153 Atherosclerosis HSDN C4085661 Usual severity nausea C0016658 Fracture bone HSDN C3812171 Bradycardia by ecg finding C3553374 Coenzyme q10 deficiency, primary, 5 MalaCards C2242996 Tingling C0158360 Fibromatosis plantar OrphaNet|MalaCards C4084776 Weight loss C0008350 Cholelithiasis HSDN C3665347 Vision impaired C0009363 Congenital ocular coloboma (disorder) HPO C4084769 Vomiting frequency C0037397 Behavior social HSDN C0027066 Myoclonic jerking C3244301 Coverage level - family HSDN C4085317 Diarrhea frequency C0023343 Leprosy HSDN C0270948 Neurogenic muscular atrophy C1861751 Minicore myopathy, moderate, with hand involvement HPO C0036572 Convulsion C3887517 Childhood brain stem gliosarcoma UMLS C0522224 Palsied C0036216 Sarcoma, experimental HSDN C0231807 Dyspnea exertional C0152417 Congenital stenosis aortic valve MalaCards C2203646 Jaundice C0032963 Pregnancy complications, cardiovascular HSDN C0029163 Hemorrhage mouth C0002448 Ameloblastoma HSDN C1971624 Appetite absent C0009450 Disease caused by microorganism HSDN C3463815 Feel fatigue C0013274 Patent ductus arteriosus HSDN C0023014 Developmental disorder language C0033923 Psychomotor function HSDN C4085210 Usual severity pain C0006105 Brain abscess HSDN C0042940 Disorder of voice C0010709 Cyst HSDN C0030554 Abnormal sensation C0004623 Bacterial infections HSDN C0040822 D tremors C1968550 Mental retardation, x-linked, syndromic 13 MalaCards|HPO|UMLS C2029884 Hearing loss by exam C0270612 Leukoencephalopathies HSDN C1963093 Dizziness adverse event C0015745 Ingestive behavior HSDN C0232466 Feeding difficulty C2751651 Chromosome 19q13.11 deletion syndrome OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0023676 Life style HSDN C0518090 Frequency of pain question C0027667 Cancer origin unknown HSDN C0349588 Stature short C0796004 Kabuki make-up syndrome OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0266209 Congenital dilatation of colon MalaCards C2911645 Weight loss adverse event C2931854 Allergic bronchopulmonary mycosis MalaCards C3274924 Have been coughing C0007787 Transient ischemic attack HSDN C0151686 Growth retardation C0152096 Complete trisomy 18 syndrome OrphaNet C0033774 Skin pruritus C0334655 T-zone; lymphoma UMLS C1963077 Bone pain adverse event C0853662 Oestrogen deficiency OrphaNet|HPO|MalaCards C0028738 Nystagmus C0342731 Deficiency of mevalonate kinase MalaCards C3463815 Feel fatigue C0040128 Thyroid diseases HSDN C4085661 Usual severity nausea C0051981 Anti-leprosy vaccine HSDN C0018681 Headache, cephalalgia C1332279 Anaplastic brain stem astrocytoma UMLS C1963071 Back pain adverse event C0035412 Rhabdomyosarcoma HSDN C0009676 Confusion state C0032001 Pituitary apoplexy MalaCards|HSDN C4084802 Usual severity diarrhea C0398788 Immunodeficiency syndrome, variable MalaCards|HPO C0030193 Sense of pain C0041971 Tumor urethra HSDN C4085661 Usual severity nausea C0032269 Pneumococcal infections HSDN C4084727 Cough frequency C1000587 Pemphigus HSDN C3887638 Failure to thrive in infant C0001193 Apert syndrome HSDN C0019214 Hepatosplenomegaly C1864651 Gaucher disease, atypical, due to saposin c deficiency HPO C0151786 Weakness muscle C0027092 Myopia HSDN C4084768 Usual severity vomiting C0033348 Language program HSDN C1963065 Apnea adverse event C0024141 Lupus erythematosus, systemic HSDN C0917816 Deficiency mental C0016788 Fucosidase deficiency disease MalaCards|HPO C0424755 Fever symptoms C1704421 Skin pigmentation disorder HSDN C0812426 Kidney problem C0744422 Glomerulonephritis proliferative diffuse UMLS C2911647 Weight gain adverse event C0039483 Giant cell arteritis HSDN C0013404 Respiratory difficulty C0000735 Abdominal neoplasms HSDN C0028738 Nystagmus C3502054 Dentoleukoencephalopathy MalaCards C0018784 Deafness sensorineural C0032962 Pregnancy complications HSDN C0003862 Pain joint C1710146 Familial spinal arachnoiditis MalaCards C4085222 Nausea C2020541 Strabismus HSDN C0012569 Double vision C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C3887873 Hearing loss C0017612 Glaucoma, open-angle HSDN C0013604 Edematous C1548484 Rheumatic fever vaccine HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0019054 Hemolysis (disorder) HSDN C0151786 Weakness muscle C0085404 Poems syndrome MalaCards|HSDN C0012833 Dizzy C0393735 Headache disorders HSDN C1549543 Administration method - pain C0007785 Cerebral infarction HSDN C0011991 Loose stools C0282687 Hemorrhagic fever, ebola DiseaseOntology|OrphaNet|MalaCards C0751265 Learning disability C2936346 22q11 deletion syndrome MalaCards C2911647 Weight gain adverse event C0003493 Aortic diseases HSDN C1959630 Eye pain adverse event C0018249 Grooming HSDN C1549543 Administration method - pain C0238461 Anaplastic thyroid carcinoma OrphaNet C0231218 Malaise generalized C3897124 Bclc stage a hepatocellular carcinoma UMLS C0042963 Symptoms vomiting C0029835 Other specified tularemia nos DiseaseOntology|MalaCards C3665492 Pigmentations C0346202 Cervical adenosquamous carcinoma MalaCards C0750426 Wbc elevated C2700553 Omenn syndrome OrphaNet|MalaCards C0013421 Dystonia C3489724 Aicardi-goutieres syndrome 2 MalaCards C0860603 Anxiety symptom C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C0426579 Anorexia symptom C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0003493 Aortic diseases HSDN C0557874 Global developmental delay C4014538 Helsmoortel-van der aa syndrome MalaCards C4085317 Diarrhea frequency C0836924 Thrombocytosis HSDN C1963184 Nystagmus adverse event C0268425 Alstrom syndrome OrphaNet|HPO|MalaCards C0032227 Effusion pleural C2931146 Radio renal syndrome MalaCards C0237326 Defecation pain C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0013604 Edematous C0268382 Amyloid nephropathy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0860239 Catheter infections related HSDN C0018834 Brash C1868684 Ear, patella, short stature syndrome MalaCards|HPO C4085211 Pain distress question C0013298 Duodenitis HSDN C0003862 Pain joint C1142083 Embolia cutis medicamentosa HSDN C1963063 Anorexia adverse event C1263846 Attention deficit hyperactivity disorder HSDN C0005745 Blepharoptosis C0270952 Muscular dystrophy, oculopharyngeal OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0040028 Thrombocythemia, essential HSDN C0018926 Emesis bloody C0019100 Severe dengue HSDN C1963071 Back pain adverse event C0001418 Adenocarcinoma HSDN C0424853 Finger mass C1290415 Neoplasm of blood vessel of finger UMLS C0042024 Urine incontinence C1555914 Psychologist - psychotherapy, group HSDN C1384666 Decreased hearing C0004030 Aspergillosis HSDN C4084774 Have weight loss C1962958 Hematoma adverse event HSDN C0007758 Cerebellar ataxia C0013384 Dyskinetic syndrome MalaCards C1963091 Diarrhea adverse event C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C3541349 Syncope C0001418 Adenocarcinoma HSDN C3641756 Have diarrhea C0025269 Multiple endocrine neoplasia type 2b HPO C0023380 Lethargy C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084766 Vomiting C0018552 Hamartoma HSDN C0011991 Loose stools C0267664 Chronic diarrhea of unknown origin UMLS C0026838 Spasticity muscle C0001623 Adrenal gland hypofunction HSDN C4084769 Vomiting frequency C0032266 Emphysema, intestinal HSDN C4085317 Diarrhea frequency C0024638 Class ii division 2 malocclusion HSDN C3641891 Have itch C0546826 Dermatophytosis body DiseaseOntology|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C0013362 Dysarthrias C0039483 Giant cell arteritis HSDN C3888418 Abdominal pain, colicky C0006818 Campylobacter infection MalaCards C4084774 Have weight loss C0001144 Acne vulgaris HSDN C4085317 Diarrhea frequency C0700095 Central neuroblastoma MalaCards|HSDN C0000737 Abdomen pain C0079840 Milk allergy HSDN C2984057 Have nausea C2911643 Encounter due to family history of osteoporosis HSDN C0413252 Hypothermia due to exposure C0019069 Hemophilia a HSDN C0013604 Edematous C0085605 Liver failure HSDN C1961131 Cough adverse event C1962986 Glaucoma adverse event HSDN C1962972 Proteinuria adverse event C0002871 Anemia HSDN C0030552 Paralysis partial C0020542 Pulmonary hypertension HSDN C0271185 Metamorphopsia C2745945 Juvenile-onset vitelliform macular dystrophy OrphaNet|HPO|MalaCards C0032617 High urine output C3665624 Serum calcium below normal HSDN C0242936 Center pain C0030790 Pelvis infection HSDN C4084784 Diarrhea C0026896 Myasthenia gravis HSDN C0086437 Joint hypermobility C2936739 Hyper-immunoglobulin e syndrome, autosomal dominant HPO C1384666 Decreased hearing C0263491 Pili torti MalaCards C0406408 Reflex urticaria C0343065 Symptomatic dermographism UMLS C4084769 Vomiting frequency C1555914 Psychologist - psychotherapy, group HSDN C0018681 Headache, cephalalgia C1842852 Epilepsy, myoclonic, benign adult familial, type 2 MalaCards C0018965 Blood urine C0403445 Fechtner syndrome (disorder) HPO C0018784 Deafness sensorineural C0015726 Focused anxiety HSDN C3714552 Strength decreased C0238386 Cronkhite-canada disease MalaCards C0151786 Weakness muscle C0018946 Hematoma, subdural HSDN C0332563 Papulae C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0038987 Sweat gland neoplasms HSDN C0522224 Palsied C0018790 Cardiac arrest HSDN C1963184 Nystagmus adverse event C0270972 Cornelia de lange syndrome MalaCards|HPO C0242936 Center pain C1306759 Eosinophilic disorder HSDN C0011991 Loose stools C4014233 Immunodeficiency 22 MalaCards|UMLS C0162285 Edema eyelid C0238288 Muscular dystrophy, facioscapulohumeral OrphaNet|HPO|MalaCards C3539893 Pelvic pain occurs with intercourse C0025202 Melanoma HSDN C4085317 Diarrhea frequency C0206682 Follicular thyroid carcinoma HSDN C4084784 Diarrhea C0014866 Esophageal stenosis HSDN C0242936 Center pain C0035436 Rheumatic fever HSDN C0851578 Disorder sleep C0039504 Injuries tendon HSDN C0018681 Headache, cephalalgia C0034069 Pulmonary fibrosis HSDN C4085210 Usual severity pain C0751895 Vasospasm, intracranial HSDN C0042963 Symptoms vomiting C0861856 Bile duct colloid carcinoma UMLS C3641755 Have constipation C0032962 Pregnancy complications HSDN C4085317 Diarrhea frequency C0152101 Hypoplastic left heart syndrome HSDN C0042024 Urine incontinence C0007784 Cerebral hemisphere hemorrhage HSDN C0043094 Weight gain C0004238 Atrial fibrillation HSDN C0812426 Kidney problem C0748334 Renal tubular acidosis congenital UMLS C4084769 Vomiting frequency C0039614 Tetanus HSDN C0000737 Abdomen pain C1306577 Dies patient HSDN C0184567 Pain acute C1719389 Acute pain due to trauma UMLS C4085211 Pain distress question C0003504 Aortic valve insufficiency HSDN C0027066 Myoclonic jerking C0027051 Myocardial infarction HSDN C0034155 Thrombotic thrombocytopenic purpura C3541306 Plasmodium measurement HSDN C0522224 Palsied C0018800 Cardiomegaly HSDN C2911647 Weight gain adverse event C0033873 Psychiatry HSDN C0152020 Atony stomach C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C2895041 Pain in right elbow C0810350 Non-traumatic joint disorders UMLS C1557397 Adverse event associated with pain C0006271 Bronchiolitis HSDN C0220982 Keto acidosis C0011854 Diabetes mellitus, insulin-dependent MalaCards C0040822 D tremors C0393614 Isolated vocal tremor UMLS C0426579 Anorexia symptom C0000768 Congenital abnormality HSDN C0015970 Fever unknown origin C0006105 Brain abscess HSDN C0033774 Skin pruritus C1561518 Pleasure - animals raised for recreation HSDN C0002622 Amnesias C2984289 Melanoma pathway HSDN C0723402 Sore throat C0276357 Swine influenza MalaCards C4085317 Diarrhea frequency C0022568 Keratitis HSDN C0019572 Hairiness C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards|HPO C0036572 Convulsion C0149871 Deep vein thrombosis UMLS C0042798 Vision dim C1112155 Hereditary non-polyposis colorectal cancer syndrome HPO C4084726 Distress cough C0011881 Diabetic nephropathy HSDN C0518090 Frequency of pain question C0033367 Projective techniques HSDN C0018926 Emesis bloody C0005695 Bladder neoplasm HSDN C0027498 Nausea vomiting C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C4084724 Usual severity constipation C0042781 Visceral myopathy MalaCards C0151786 Weakness muscle C0017927 Glycogen storage disease type viii HSDN C1384666 Decreased hearing C3888210 Deafness, autosomal dominant 58 MalaCards C0013404 Respiratory difficulty C0079504 Hermanski-pudlak syndrome MalaCards|HSDN C0033778 Vulvar pruritus C0810052 Other inflammatory condition of skin UMLS C0085631 Abnormal excitement C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO C1069915 Vertigo C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards C0011991 Loose stools C0349231 Phobic anxiety disorder HSDN C0036572 Convulsion C2919115 Encounter due to bereavement HSDN C0026838 Spasticity muscle C1838625 Warburg sjo fledelius syndrome OrphaNet|HPO C0024031 Back pain lower back C0162871 Aortic aneurysm, abdominal HSDN C0036572 Convulsion C1848211 Mental retardation with psychosis, pyramidal signs, and macroorchidism MalaCards|HPO C0018681 Headache, cephalalgia C0008350 Cholelithiasis HSDN C2911645 Weight loss adverse event C0015773 Felty syndrome OrphaNet|MalaCards C4085317 Diarrhea frequency C0242216 Biliary calculi HSDN C4085211 Pain distress question C0014009 Empyema HSDN C0030554 Abnormal sensation C0001529 Dercum disease MalaCards C2984058 Have pain C0037313 Sleep HSDN C0037284 Skin lesion C0003177 Cutaneous anthrax MalaCards C0917816 Deficiency mental C1837819 Cerebrofrontofacial syndrome MalaCards|HPO C0013395 Indigestion C0031149 Peritoneal neoplasms HSDN C0011991 Loose stools C0000771 Abnormalities, drug induced HSDN C0557874 Global developmental delay C2677903 Mental retardation and microcephaly with pontine and cerebellar hypoplasia MalaCards|HPO C0030554 Abnormal sensation C0009324 Ulcerative colitis HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0085389 Bacillaceae infection HSDN C0020580 Decreased sensation C0030567 Parkinson disease HSDN C2919142 Short stature adverse event C1869115 Weill-marchesani syndrome, autosomal dominant OrphaNet|HPO|MalaCards C4084776 Weight loss C0007781 Intracranial embolism and thrombosis HSDN C0007758 Cerebellar ataxia C0027404 Narcolepsy HSDN C0013604 Edematous C0029001 Onchocerciasis HSDN C0007398 Catatonic C2986768 Injected dose HSDN C4084725 Usual severity cough C0037354 Smallpox HSDN C0015230 Exanthem C0574733 Rash rubelliform UMLS C0010520 Skin cyanosis C0020649 Hypotension HSDN C1961131 Cough adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C1963093 Dizziness adverse event C0262584 Carcinoma, small cell HSDN C1963063 Anorexia adverse event C0033348 Language program HSDN C0013421 Dystonia C0751278 Metachromatic leukodystrophy, infant MalaCards|HPO C2984057 Have nausea C0017150 Gastrinoma OrphaNet|MalaCards C0085602 Polydypsia C3665624 Serum calcium below normal HSDN C0024031 Back pain lower back C0009375 Colonic neoplasms HSDN C0040485 Wryneck C0003873 Rheumatoid arthritis HSDN C2032395 Pelvic pain on the left C0242350 Erectile dysfunction HSDN C0036572 Convulsion C0393688 Epilepsy, opercular UMLS C0151889 Reflexes tendon increased C1849732 Polydactyly, postaxial, with dental and vertebral anomalies OrphaNet|MalaCards C0392699 Dysaesthesia C0752355 Myotonia fluctuans (disorder) HPO C3541349 Syncope C0004044 Asphyxia HSDN C4084766 Vomiting C0029928 Ovarian diseases HSDN C0027497 Queasy C0162576 Anisakiasis MalaCards C4084774 Have weight loss C0024692 Mandible fracture HSDN C4085549 Dizziness C0041327 Tuberculosis, pulmonary HSDN C0085636 Light sensitivity C0206725 Subependymal glioma HSDN C2203646 Jaundice C0085423 Gram-negative bacterial infections HSDN C0242936 Center pain C0025064 Mediastinitis HSDN C0030193 Sense of pain C0013537 Eclampsia HSDN C1557397 Adverse event associated with pain C1541646 Spirituality therapy HSDN C0151827 Pain eye C0018193 Granuloma, foreign-body HSDN C4084775 Usual severity weight loss C0035613 Rift valley fever MalaCards C4084769 Vomiting frequency C0007194 Hypertrophic cardiomyopathy HSDN C0033377 Caudal displacement C0265372 Fetal hydantoin syndrome OrphaNet|MalaCards C1963093 Dizziness adverse event C0010034 Corneal diseases HSDN C0018772 Deafness C0013595 Eczema HSDN C0413252 Hypothermia due to exposure C1636667 Disorder characterized by eosinophilia HSDN C2037210 Flushing several times a day C0041834 Erythema UMLS C1962976 Ventricular fibrillation adverse event C2678485 Long qt syndrome 9 (disorder) MalaCards C0036572 Convulsion C1719638 Recurrent convulsions nos UMLS C0231835 Respiration rate increased C1970470 Surfactant metabolism dysfunction, pulmonary, 2 (disorder) MalaCards|HPO C2237041 Shox gene with short stature C0265449 Pallister-killian syndrome OrphaNet|MalaCards C0015468 Face pain C0220847 C hepatitis virus HSDN C1962972 Proteinuria adverse event C0020255 Hydrocephalus HSDN C0007859 Pain neck C0017601 Glaucomas HSDN C0006370 Bulimia C0870371 Crave HSDN C1510417 Apraxia of gait C0026613 Motor skills disorders HSDN C4084773 Bothered by weight gain C0023892 Biliary cirrhosis HSDN C0518090 Frequency of pain question C0014009 Empyema HSDN C0751706 Aphasia, progressive nonfluent C0497327 Dementia HSDN C1963091 Diarrhea adverse event C0085096 Peripheral vascular diseases HSDN C0853986 Lymphocytes decreased C1282908 De vaal's syndrome MalaCards C0018681 Headache, cephalalgia C0001433 Adenoma, acidophil HSDN C0028081 Night sweat C0854810 Recurrent hodgkin's disease lymphocyte depletion type UMLS C4085211 Pain distress question C0017075 Ganglioneuroma HSDN C4084784 Diarrhea C0026848 Myopathy HSDN C0042571 Vertigo subjective C0155499 Meniere's disease in remission UMLS C0003862 Pain joint C0004943 Behcet syndrome OrphaNet|HSDN|HPO|MalaCards C0042963 Symptoms vomiting C0016169 Pathologic fistula HSDN C4085549 Dizziness C0013295 Duodenal ulcer HSDN C1549543 Administration method - pain C0015923 Fetal alcohol syndrome HSDN C0009398 Color vision defects C0005695 Bladder neoplasm HSDN C0026821 Cramp C0015397 Disorder of eye HSDN C2919142 Short stature adverse event C0086652 Mucopolysaccharidosis type ivb MalaCards C0032617 High urine output C0022667 Papillary necrosis HSDN C0028738 Nystagmus C2676042 Skin-hair-eye pigmentation, variation in, 4 HPO C3463815 Feel fatigue C0027831 Neurofibromatosis 1 HSDN C0036659 Sensation disorder C0036674 Sensory deprivation HSDN C0026826 High muscle tone C0027868 Neuromuscular diseases HSDN C0007758 Cerebellar ataxia C0035302 Retinal artery occlusion HSDN C0036572 Convulsion C0005941 Bone diseases, developmental HSDN C0150055 Pain chronic C1963198 Pancreatitis adverse event HSDN C0018772 Deafness C0031090 Periodontal diseases HSDN C0454644 Delayed language development C0751667 Canavan disease, juvenile OrphaNet|HPO C0003862 Pain joint C0004238 Atrial fibrillation HSDN C2911645 Weight loss adverse event C0000833 Abscess HSDN C2029884 Hearing loss by exam C0042384 Vasculitis HSDN C4085210 Usual severity pain C1449861 Micronuclei, chromosome-defective HSDN C0024031 Back pain lower back C0302148 Blood clot HSDN C0012569 Double vision C1963067 Atrial fibrillation adverse event HSDN C0015468 Face pain C0018249 Grooming HSDN C0522224 Palsied C0007097 Carcinomas HSDN C4085661 Usual severity nausea C0039128 Syphilis HSDN C4084766 Vomiting C0023473 Myeloid leukemia, chronic HSDN C0037383 Sneeze C0009766 Allergic conjunctivitis HSDN C1549543 Administration method - pain C0162871 Aortic aneurysm, abdominal HSDN C0042025 Urinary incontinence stress C0037315 Sleep apnea syndromes HSDN C0013604 Edematous C0026771 Trauma multiple HSDN C2984058 Have pain C0266929 Chronic periodontitis HSDN C3829611 Nausea frequency C0003615 Appendicitis DiseaseOntology|HSDN|MalaCards C0037316 Not enough sleeping C0022661 Kidney failure, chronic HSDN C4084724 Usual severity constipation C0338503 Septo-optic dysplasia HPO C0424755 Fever symptoms C0024788 Green monkey virus disease DiseaseOntology|HSDN|OrphaNet|MalaCards C4082202 Sleep quality question C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0004604 Pain back C0007133 Carcinoma, papillary HSDN C4084784 Diarrhea C0027121 Myositis HSDN C0010200 Cough symptom C0007762 Cerebellar neoplasms HSDN C2911645 Weight loss adverse event C0007138 Carcinoma, transitional cell HSDN C0427055 Face weakness C1864649 Myasthenia, limb-girdle, with tubular aggregates HPO C0242936 Center pain C0751772 Rem sleep behavior disorder HSDN C4084767 Bothered by vomiting C0600564 Self-efficacy HSDN C0917816 Deficiency mental C0268136 Xeroderma pigmentosum, group b HPO C3898969 Have been vomiting C0005779 Blood coagulation disorders HSDN C0033377 Caudal displacement C0008628 Chromosome deletion MalaCards C3539895 Pelvic pain occurs with bowel movement C0302148 Blood clot HSDN C0751837 Gait ataxic C0333596 Deposition of iron HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037937 Spine injury HSDN C0042963 Symptoms vomiting C0162871 Aortic aneurysm, abdominal HSDN C3641756 Have diarrhea C0035579 Rickets HSDN C1971624 Appetite absent C0238027 Botulism, infantile OrphaNet|MalaCards C0349588 Stature short C1841854 Gms syndrome OrphaNet|MalaCards C0015300 Ocular proptosis C1857663 Yunis varon syndrome MalaCards|HPO C0031911 Pigment deposition C1313983 Conjunctivitis, catarrhal, acute MalaCards C0009806 Constipate C0008074 Child development disorders, pervasive HSDN C1963087 Constipation adverse event C0020598 Hypocalcemia HSDN C0008031 Pain chest C0002895 Anemia, sickle cell OrphaNet|UMLS|HPO|MalaCards C0019214 Hepatosplenomegaly C0020564 Hypertrophy UMLS C4085211 Pain distress question C1547044 Kind of quantity - smell HSDN C0030193 Sense of pain C1968835 Egot gene HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0039980 Chest injury HSDN C4084723 Constipation C0020681 Sleep-related respiratory failure MalaCards C0040264 Ear ringing sound C0011265 Presenile dementia HSDN C0013604 Edematous C0085648 Synovial cyst HSDN C0036572 Convulsion C0796095 Opitz trigonocephaly syndrome OrphaNet|UMLS|HPO|MalaCards C4084776 Weight loss C0032285 Pneumonia HSDN C2984057 Have nausea C0700095 Central neuroblastoma HSDN C0037316 Not enough sleeping C0018916 Hemangioma HSDN C1971624 Appetite absent C1830398 Grooming:-:point in time:^patient:- HSDN C2700617 Irritation - emotion C0001622 Adrenal gland hyperfunction OrphaNet C1963091 Diarrhea adverse event C0024810 Marijuana smoking HSDN C0036572 Convulsion C0856830 Calcium pyrophosphate arthropathy MalaCards|HPO C3898969 Have been vomiting C0024667 Animal mammary neoplasms HSDN C0917816 Deficiency mental C3888209 Spastic paraplegia 45, autosomal recessive MalaCards C0003862 Pain joint C0021368 Inflammation MalaCards C1963063 Anorexia adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C3463815 Feel fatigue C1546847 Entity name part type - family HSDN C0013404 Respiratory difficulty C0038663 Suicide attempt HSDN C4084784 Diarrhea C3149378 Immunodeficiency, common variable, 1 MalaCards|HPO C0036572 Convulsion C0040435 Tooth diseases HSDN C3274924 Have been coughing C0036329 Schistosomiasis japonica DiseaseOntology C0022346 Yellow skin C1335305 Intraductal papillary-mucinous neoplasm of pancreas with moderate dysplasia UMLS C0015469 Facial paralysis C0013990 Pathological accumulation of air in tissues HSDN C4085211 Pain distress question C0017668 Focal glomerulosclerosis HSDN C3815497 Cough C0016045 Fibroma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242891 Injuries teeth HSDN C4084766 Vomiting C0033975 Psychotic disorders HSDN C4085211 Pain distress question C0017417 Genital neoplasms, male HSDN C4085661 Usual severity nausea C0020649 Hypotension HSDN C0917816 Deficiency mental C2678051 Mental retardation, x-linked 94 (disorder) MalaCards|HPO C4085548 Usual severity dizziness C0019163 Hepatitis b HSDN C0349588 Stature short C3275495 Kabuk2 MalaCards C2984058 Have pain C0029454 Osteopetrosis HSDN C0018772 Deafness C0026363 Mohr-claussen syndrome MalaCards C0151786 Weakness muscle C0026764 Multiple myeloma HSDN C0034150 Skin purpura C0041466 Typhoid fever HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C3808145 Left ventricular noncompaction 9 MalaCards C0042940 Disorder of voice C0206706 Verrucous carcinoma HSDN C0085593 Chill C0494039 Gastrointestinal tularaemia MalaCards C2911645 Weight loss adverse event C0016514 Foot-and-mouth disease HSDN C1963063 Anorexia adverse event C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0018808 Murmur C0031048 Pericarditis, constrictive HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0021603 Sleep initiation and maintenance disorders HSDN C0018834 Brash C1956097 Wolf-hirschhorn syndrome MalaCards|HPO C0010200 Cough symptom C1332511 Benign germ cell neoplasm of mediastinum UMLS C0008031 Pain chest C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0036572 Convulsion C1855849 Bartter syndrome, antenatal , type 2 HPO|UMLS C0027066 Myoclonic jerking C0752121 Spinocerebellar ataxia type 2 MalaCards|HPO|UMLS C0040822 D tremors C0221061 Behr syndrome MalaCards C2237041 Shox gene with short stature C1858032 Cortical defects, wormian bones, and dentinogenesis imperfecta OrphaNet|MalaCards C0042963 Symptoms vomiting C0242134 Train sickness UMLS C0033377 Caudal displacement C0265279 Kniest dysplasia MalaCards|HPO C4084723 Constipation C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2096293 Ent surgical result ear vertigo C0007781 Intracranial embolism and thrombosis HSDN C0917816 Deficiency mental C0265343 Jarcho-levin syndrome HPO C1963249 Tinnitus adverse event C0014038 Encephalitis HSDN C0518090 Frequency of pain question C0037974 Spirochaetales infections HSDN C4085210 Usual severity pain C0265334 Pachyonychia congenita HSDN C0013604 Edematous C0038941 Incisional infection HSDN C4085211 Pain distress question C0015558 Fallopian tube neoplasms HSDN C0269268 Breast hardness C0156318 Fibrosis breast UMLS C0851578 Disorder sleep C0031090 Periodontal diseases HSDN C4084766 Vomiting C0008073 Developmental disabilities HSDN C0231218 Malaise generalized C1709574 Pleural epithelioid mesothelioma UMLS C0242936 Center pain C0001403 Addison disease HSDN C4085210 Usual severity pain C0036875 Disorders of sex development HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1963107 Euphoria adverse event HSDN C0242936 Center pain C0035229 Respiratory insufficiency HSDN C1263846 Attention deficit disorder with hyperactivity C3266843 47, xyy syndrome OrphaNet C0007758 Cerebellar ataxia C0035229 Respiratory insufficiency HSDN C0019079 Bloody sputum C1509147 Histiocytoma HSDN C0242936 Center pain C0027439 Nasopharyngeal neoplasms HSDN C4020887 Photodysphoria C0004576 Babesiosis MalaCards C0040822 D tremors C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO|UMLS C4084788 Have dizziness C0008370 Cholestasis HSDN C2036478 Stuttering accompanied by hand movements C0038506 Stuttering UMLS C0013395 Indigestion C0008325 Cholecystitis HSDN C0036659 Sensation disorder C3887662 Intraspinal neoplasm HSDN C3641756 Have diarrhea C1956257 Pulmonary stenosis HSDN C3463815 Feel fatigue C0221056 Adult type dermatomyositis OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1963068 Atrial flutter adverse event HSDN C0034933 Abnormal reflexes C0001175 Acquired immunodeficiency syndrome HSDN C0344315 Mood depressed C3810230 Neurodegeneration with brain iron accumulation 6 MalaCards C0018991 Paralysis one side of body C0011860 Diabetes mellitus, non-insulin-dependent HSDN C3539022 Pelvic pain decreasing in severity C0282606 Myomatous neoplasm HSDN C0242936 Center pain C0161406 Injury nerve trigeminal HSDN C0036572 Convulsion C0022797 Adult neuronal ceroid lipofuscinosis UMLS C0557874 Global developmental delay C4015167 Mental retardation, autosomal dominant 30 MalaCards C0009806 Constipate C0162671 Melas syndrome MalaCards|HPO C0023014 Developmental disorder language C0752287 Sleep disorders, intrinsic HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0028738 Nystagmus HSDN C0020578 Hyperventilate C0039231 Tachycardia HSDN C2203646 Jaundice C0017181 Gastrointestinal hemorrhage HSDN C4084726 Distress cough C0009240 Cognition HSDN C0557874 Global developmental delay C1842836 Congenital disorder of glycosylation, type ii MalaCards|HPO C0851578 Disorder sleep C0007771 Intracranial arteriosclerosis HSDN C0727671 Red cross toothache drops C0016398 Focal infection, dental HSDN C1557397 Adverse event associated with pain C0030283 Pancreatic cyst HSDN C0242936 Center pain C0005716 Blastomycosis HSDN C4084769 Vomiting frequency C0032969 Pregnancy in diabetics HSDN C0037763 Spasm C0014553 Absence epilepsy HSDN C4085862 Bothered by nausea C0010074 Coronary vessel anomalies HSDN C0007758 Cerebellar ataxia C1504306 Anodontia genus HSDN C0019825 Voice hoarseness C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0023380 Lethargy C0036474 Scurvy HSDN C3539892 Pelvic pain in front C0005491 Biofeedback HSDN C1963065 Apnea adverse event C0004842 Battered child syndrome HSDN C0042024 Urine incontinence C0016053 Fibromyalgia HSDN C1963167 Memory impairment adverse event C2931917 Alcoholic encephalopathy MalaCards C4085222 Nausea C0001418 Adenocarcinoma HSDN C3815497 Cough C0524851 Neurodegenerative disorders HSDN C0020455 Hypergammaglobulinemia C0042109 Urticaria HSDN C3539891 Pelvic pain to the rear C1963088 Cystitis adverse event HSDN C4085317 Diarrhea frequency C0009404 Colorectal neoplasms HSDN C3641756 Have diarrhea C0000786 Spontaneous abortion HSDN C0086565 Liver function abnormal C0235974 Pancreatic carcinoma MalaCards C1145670 Failure respiratory C0042111 Urticaria pigmentosa MalaCards C0037199 Sinus infection C3809706 Ciliary dyskinesia, primary, 28 MalaCards C4084773 Bothered by weight gain C0019372 Herpesviridae infections HSDN C2029884 Hearing loss by exam C4084909 Depression subordinate domain HSDN C4085210 Usual severity pain C0149925 Small cell carcinoma of lung HSDN C0241137 Skin pallor C0041188 Pyomyositis, tropical HSDN C1963090 Dehydration adverse event C0268621 Hepatic methionine adenosyltransferase deficiency MalaCards C0013428 Painful urination C1321581 Bezoar disorder HSDN C1961131 Cough adverse event C3244301 Coverage level - family HSDN C2984058 Have pain C0024796 Marfan syndrome HSDN C0423742 Intercourse pain C0282488 Interstitial cystitis OrphaNet|MalaCards C0518090 Frequency of pain question C0032290 Aspiration pneumonia HSDN C0917816 Deficiency mental C0221061 Behr syndrome OrphaNet|HPO|MalaCards C0022346 Yellow skin C0035228 Respiratory hypersensitivity HSDN C0009421 Comatose C0017168 Gastroesophageal reflux disease HSDN C4084768 Usual severity vomiting C1704212 Embolism embolus HSDN C0025287 Meningitis-like C0036114 Enteritis salmonella HSDN C0018784 Deafness sensorineural C0085094 Head injury closed HSDN C2984058 Have pain C0423772 Cutaneous fistula HSDN C0009806 Constipate C0024115 Lung diseases HSDN C0037384 Snore C0032897 Prader-willi syndrome HSDN C0007758 Cerebellar ataxia C3810212 Joubert syndrome 21 MalaCards|UMLS C0041657 Consciousness loss C0085437 Meningitis, bacterial HSDN C0012569 Double vision C0453996 Tobacco smoking HSDN C0518090 Frequency of pain question C0085298 Sudden cardiac death HSDN C0030486 Extremity paralysis, lower C0010054 Coronary arteriosclerosis HSDN C0018784 Deafness sensorineural C0270639 Lateral sinus thrombosis HSDN C0042024 Urine incontinence C0549567 Pigmentation disorders HSDN C0020672 Body temperature decreased C0033968 Psychotherapeutic technique HSDN C4084784 Diarrhea C0085412 Encephalitozoonosis HSDN C0030486 Extremity paralysis, lower C0023418 Leukemia HSDN C0242936 Center pain C1696469 Shin splints HSDN C3641756 Have diarrhea C0080178 Spina bifida HSDN C2984057 Have nausea C0860603 Anxiety symptoms HSDN C0151786 Weakness muscle C0032787 Postoperative complications HSDN C0030554 Abnormal sensation C0002726 Amyloidosis HSDN C0851578 Disorder sleep C0025284 Meningeal neoplasms HSDN C0085593 Chill C0854890 Localized pleural malignant mesothelioma UMLS C0162275 Ketoaciduria C1855101 Methylmalonyl-coa epimerase deficiency with sepiapterin reductase deficiency HPO C0036572 Convulsion C1306880 Simple partial onset of seizure with automatisms UMLS C0040034 Thrombocytopenia C1842090 Platelet glycoprotein iv deficiency MalaCards|HPO C0004134 Dyssynergia C0700327 Clinical findings relating to memory HSDN C0027066 Myoclonic jerking C0751774 Nocturnal myoclonus syndrome HSDN C0917816 Deficiency mental C1860786 Down syndrome chromosome region HPO C0036572 Convulsion C1512194 Gliomatosis cerebri type ii UMLS C2029884 Hearing loss by exam C0022665 Kidney neoplasm HSDN C0037763 Spasm C1636667 Disorder characterized by eosinophilia HSDN C0013604 Edematous C0011311 Dengue fever HSDN C0020672 Body temperature decreased C0242698 Ventricular dysfunction, left HSDN C0151686 Growth retardation C1854989 Molybdenum cofactor deficiency, complementation group b HPO C0684343 Pseudophakia C0011854 Diabetes mellitus, insulin-dependent HSDN C3829611 Nausea frequency C0016169 Pathologic fistula HSDN C0020538 Hbp C1859567 Bardet-biedl syndrome 9 HPO C4084775 Usual severity weight loss C0009475 Community mental health service HSDN C0231528 Muscle pain generalized C0026205 Miosis disorder MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0023220 Leg injury HSDN C3463815 Feel fatigue C2316212 Cryopyrin-associated periodic syndromes MalaCards C0027497 Queasy C0001882 Air sickness UMLS C0018681 Headache, cephalalgia C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0033377 Caudal displacement C2931183 Faces syndrome OrphaNet|MalaCards C1963093 Dizziness adverse event C0039538 Teratoma HSDN C0262527 Intermittent abdominal pain C1848793 Tiglic acidemia MalaCards C0013395 Indigestion C0006285 Bronchopneumonia HSDN C2911645 Weight loss adverse event C1998602 Meals HSDN C4085222 Nausea C0042769 Virus diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0007959 Charcot-marie-tooth disease HSDN C0398650 Idiopathic thrombocytopenia purpura C0026782 Mumps vaccine HSDN C4084769 Vomiting frequency C0018817 Atrial septal defects HSDN C2919142 Short stature adverse event C1856728 Fuhrmann syndrome HPO C0016382 Cutaneous vascular engorgement C0162569 Hepatoerythropoietic porphyria MalaCards C4085862 Bothered by nausea C0011616 Contact dermatitis HSDN C0233794 Memory impaired C0024198 Lyme disease MalaCards C0010200 Cough symptom C0264423 Asthma, occupational HSDN C1963091 Diarrhea adverse event C0398691 Hyperimmunoglobulinemia d OrphaNet|HPO|MalaCards C0150055 Pain chronic C0458219 Complex regional pain syndromes UMLS C1963091 Diarrhea adverse event C0687720 Central diabetes insipidus MalaCards C0003550 Broca aphasia C0751706 Primary progressive nonfluent aphasia MalaCards|HPO C0150055 Pain chronic C1552262 Nurse practitioner - family HSDN C0242936 Center pain C0009862 Contraception behavior HSDN C4042891 Sleep wake disorders C0032897 Prader-willi syndrome HSDN C0010200 Cough symptom C0267830 Pyogenic liver abscess HSDN C0007859 Pain neck C0029423 Cartilaginous exostosis HSDN C0037036 Increased salivation C2750247 Polymicrogyria, asymmetric HPO C0037316 Not enough sleeping C0453996 Tobacco smoking HSDN C0036572 Convulsion C1263882 C-p angle meningioma UMLS C1549543 Administration method - pain C0027627 Neoplasm metastasis HSDN C0426579 Anorexia symptom C0001418 Adenocarcinoma HSDN C0036572 Convulsion C0265328 Alopecia-epilepsy-oligophrenia syndrome OrphaNet|UMLS|MalaCards C0036572 Convulsion C0009241 Cognition disorders HSDN C0151786 Weakness muscle C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards C0013395 Indigestion C0520676 Premenstrual dysphoric disorder HSDN C0036572 Convulsion C0007795 Diffuse cerebral sclerosis of schilder MalaCards C3463815 Feel fatigue C0031149 Peritoneal neoplasms HSDN C1963091 Diarrhea adverse event C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C4084727 Cough frequency C0149931 Migraine disorders HSDN C0022346 Yellow skin C0004576 Babesiosis OrphaNet|HSDN|MalaCards C0042025 Urinary incontinence stress C3714514 Infection HSDN C0086565 Liver function abnormal C0342871 Acyl-coa oxidase deficiency MalaCards C0007398 Catatonic C1867772 Catatonia of kraepelin MalaCards C4085548 Usual severity dizziness C0023343 Leprosy HSDN C0013456 Pain ear C0030581 Parotid neoplasms HSDN C0018681 Headache, cephalalgia C0023092 Lassa fever OrphaNet|MalaCards C0018681 Headache, cephalalgia C0017181 Gastrointestinal hemorrhage HSDN C0018681 Headache, cephalalgia C2368013 Periodic headache syndromes in child or adolescent with intractable migraine and status migrainosus UMLS C4085222 Nausea C1552262 Nurse practitioner - family HSDN C0016204 Fart C0005750 Blind loop syndrome HSDN C0000737 Abdomen pain C1333082 Adenosquamous carcinoma of colon UMLS C2984058 Have pain C1963059 Adrenal insufficiency adverse event HSDN C4084776 Weight loss C0024215 Lymphangiectasis, intestinal MalaCards|HSDN C0349506 Sun sensitivity C1847827 Lig4 syndrome OrphaNet|HPO|MalaCards C0085636 Light sensitivity C0039792 Psychotherapeutic interaction HSDN C3829611 Nausea frequency C0032914 Pre-eclampsia HSDN C0497247 Blood pressure elevation C0162359 Christ-siemens-touraine syndrome MalaCards|HPO C2203646 Jaundice C0022350 Jaundice, chronic idiopathic OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0042594 Vestibular diseases HSDN C0020672 Body temperature decreased C0241158 Cicatrix skin HSDN C0034933 Abnormal reflexes C0004377 Automatism HSDN C0030552 Paralysis partial C0018809 Heart neoplasm HSDN C0007859 Pain neck C0019069 Hemophilia a HSDN C3539892 Pelvic pain in front C0022865 Obstetric labor complications HSDN C0577569 Mass of male genital structure C0582498 Cyst of embryonic remnant-male UMLS C4084776 Weight loss C0026918 Mycobacterium infections HSDN C0522224 Palsied C0040517 Gilles de la tourette syndrome HSDN C4084727 Cough frequency C0032969 Pregnancy in diabetics HSDN C0522039 Wrist edema C0522035 Upper extremity edema UMLS C4085210 Usual severity pain C0032269 Pneumococcal infections HSDN C0262527 Intermittent abdominal pain C0007095 Carcinoid tumor MalaCards C0030193 Sense of pain C0311375 Arsenic poisoning HSDN C4084788 Have dizziness C0031350 Pharyngitis HSDN C0018681 Headache, cephalalgia C1868934 Hemicephalalgia UMLS C0013595 Eczematous dermatitis C3280231 Chromosome 8q21.11 deletion syndrome MalaCards C1963184 Nystagmus adverse event C3280766 Joubert syndrome 14 MalaCards C0013390 Cramps menstrual C0152156 Dystocia HSDN C0004134 Dyssynergia C2586211 Thrombosis of blood vessel HSDN C4084769 Vomiting frequency C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0038354 Stomach diseases HSDN C0040264 Ear ringing sound C0338586 Vertebral artery dissection HSDN C2984057 Have nausea C0027962 Melanocytic nevus HSDN C0036572 Convulsion C0520681 Central alveolar hypoventilation syndrome MalaCards C0002965 Crescendo angina C0236969 Substance-related disorders HSDN C0040485 Wryneck C3554447 Dystonia 25 MalaCards|UMLS C4255193 Bilateral vestibulopathy C2931205 Usher syndrome, type 1a MalaCards C1557397 Adverse event associated with pain C0022362 Jaw diseases HSDN C0857305 Thrombocytopenia purpura C0002884 Hypochromic anemia HSDN C0242936 Center pain C0024473 Magnesium deficiency HSDN C0036572 Convulsion C0242647 Mucosa-associated lymphoid tissue lymphoma HSDN C1963281 Vomiting adverse event C0026266 Mitral valve insufficiency HSDN C0015230 Exanthem C0919833 Ross river virus infection MalaCards C0042798 Vision dim C3502492 Microcephaly with chorioretinopathy, autosomal recessive OrphaNet|HPO|MalaCards C0011206 Delirium acute C0342257 Complications of diabetes mellitus HSDN C1963087 Constipation adverse event C0948089 Acute coronary syndrome HSDN C3641756 Have diarrhea C0019372 Herpesviridae infections HSDN C4042891 Sleep wake disorders C0011263 Multi-infarct dementia HSDN C0221263 Cafe au lait spot C1136043 Acoustic schwannoma, bilateral HPO C2984057 Have nausea C0022408 Arthropathy HSDN C2911645 Weight loss adverse event C1136321 Hiv-associated lipodystrophy syndrome HSDN C0150055 Pain chronic C0038454 Cerebrovascular accident HSDN C0242936 Center pain C0032302 Mycoplasma pneumonia HSDN C2242996 Tingling C0338586 Vertebral artery dissection HSDN C0018524 Hallucinate C1962958 Hematoma adverse event HSDN C0041834 Erythematous condition C1721006 Keratoderma, palmoplantar, epidermolytic OrphaNet|HPO|MalaCards C0036572 Convulsion C0025286 Meningioma MalaCards C0034155 Thrombotic thrombocytopenic purpura C0005956 Bone marrow diseases HSDN C2919142 Short stature adverse event C0272170 Shwachman syndrome OrphaNet|HPO C1549543 Administration method - pain C0398623 Thrombophilia HSDN C0030552 Paralysis partial C1853396 Primary lateral sclerosis juvenile OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0002940 Aneurysm HSDN C4084724 Usual severity constipation C2004491 Cicatrix HSDN C1963071 Back pain adverse event C0014852 Esophageal diseases HSDN C0030552 Paralysis partial C1862940 Amyotrophic lateral sclerosis, autosomal recessive HPO C0152116 Torticollis spasmodic C0810266 Hereditary and degenerative nervous system conditions UMLS C3898969 Have been vomiting C0002940 Aneurysm HSDN C1963281 Vomiting adverse event C0016053 Fibromyalgia HSDN C3829611 Nausea frequency C0037369 Smoking HSDN C0518090 Frequency of pain question C0035592 Infection, rickettsiaceae HSDN C0007859 Pain neck C0030271 Pancoast syndrome HSDN C0036572 Convulsion C0040185 Tibia fracture HSDN C1557397 Adverse event associated with pain C0008370 Cholestasis HSDN C0018777 Deafness, conductive C0031511 Pheochromocytoma MalaCards C0575081 Abnormal gait C2931291 Familial spastic paraparesis and deafness OrphaNet|MalaCards C1963087 Constipation adverse event C0007138 Carcinoma, transitional cell HSDN C0036572 Convulsion C2931859 Acquired cjd MalaCards C0020649 Blood pressure decreased C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0858893 Discomfort around orbit C0948595 Ocular discomfort UMLS C3539892 Pelvic pain in front C1548578 Location characteristic id - smoking HSDN C4085642 Level of joint stiffness C2713321 Alpha-l-iduronidase deficiency OrphaNet C0020450 Hyperemesis gravidarum C0003873 Rheumatoid arthritis HSDN C1557397 Adverse event associated with pain C0003175 Anthrax disease HSDN C0013144 Drowsy C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C0015469 Facial paralysis C4042784 Feeding and eating disorders HSDN C1963087 Constipation adverse event C0009241 Cognition disorders HSDN C0030193 Sense of pain C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C0037317 Sleep disturbance C0162809 Kallmann syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0151740 Intracranial hypertension HSDN C0011168 Disorder deglutition C1834673 Facioscapulohumeral muscular dystrophy 1a MalaCards|HPO C0349588 Stature short C1859774 Optic nerve hypoplasia and abnormalities of the central nervous system HPO C0009676 Confusion state C0025295 Meningitis, pneumococcal HSDN C0850758 Pain pelvic C1547940 Specimen source codes - ulcer HSDN C1145670 Failure respiratory C1306794 Wound botulism MalaCards C3815497 Cough C0015745 Ingestive behavior HSDN C0036572 Convulsion C0342770 Fumarase deficiency MalaCards|UMLS C1963086 Confusion adverse event C3714514 Infection HSDN C0004604 Pain back C0162703 Pain sensitivity HSDN C0242936 Center pain C2350019 Solitary pulmonary nodule HSDN C3641755 Have constipation C3888013 Hypnoses HSDN C0037763 Spasm C0004095 Asthenopia HSDN C0743973 Fever high C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C4084773 Bothered by weight gain C0242350 Erectile dysfunction HSDN C0009676 Confusion state C0015630 Fantasies HSDN C1069915 Vertigo C0004153 Atherosclerosis HSDN C2025995 Cellulitis C0264005 Fasciitis, eosinophilic OrphaNet|MalaCards C4084769 Vomiting frequency C3280314 Combined malonic and methylmalonic aciduria MalaCards C0015672 Decreased energy C0852711 Sickle cell dactylitis HSDN C3665346 Loss sight C1844671 Dermoids of cornea MalaCards C4084769 Vomiting frequency C0025037 Meckel diverticulum HSDN C0007758 Cerebellar ataxia C0085209 Bovine spongiform encephalitis HSDN C2237041 Shox gene with short stature C1832594 Verloes bourguignon syndrome MalaCards|HPO C0016199 Pain flank C0034359 Cell pus urine HSDN C0030232 Color loss C1005359 Pica pica bird HSDN C4084802 Usual severity diarrhea C0013922 Embolism HSDN C0151889 Reflexes tendon increased C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C0040485 Wryneck C0009081 Congenital clubfoot HSDN C0917816 Deficiency mental C0268576 Hyperleucinemia OrphaNet C0023014 Developmental disorder language C0812393 Cancer patients and suicide and depression HSDN C0013132 Drooling C1968551 Mental retardation, x-linked 79 MalaCards|HPO C0424755 Fever symptoms C0015480 Disorder factitious HSDN C0012833 Dizzy C0042018 Urinary calculi HSDN C1549543 Administration method - pain C0039981 Thoracic neoplasms HSDN C0020580 Decreased sensation C0004096 Asthma HSDN C0015402 Hemorrhage eye C0031542 Phlebitis HSDN C0034933 Abnormal reflexes C1963088 Cystitis adverse event HSDN C0009763 Conjunctiva inflammation C0268390 Muckle-wells syndrome OrphaNet|HPO|MalaCards C0917816 Deficiency mental C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C4084725 Usual severity cough C3495801 Granulomatosis with polyangiitis OrphaNet|HSDN|HPO|MalaCards C4085317 Diarrhea frequency C0016667 Fragile x syndrome HSDN C2024878 Cardiovascular surgery result: dyspnea C0022790 Krukenberg tumor HSDN C3274924 Have been coughing C2973787 Coxiella burnetii infection MalaCards C4084784 Diarrhea C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C0004134 Dyssynergia C1136249 Mental retardation, x-linked HSDN C0018772 Deafness C0005941 Bone diseases, developmental HSDN C2237041 Shox gene with short stature C0008928 Cleidocranial dysplasia OrphaNet|HPO|MalaCards C0011991 Loose stools C0041234 Chagas disease OrphaNet|MalaCards C3665347 Vision impaired C2931803 Deletion 11p13 OrphaNet|HPO C2984058 Have pain C0006736 Body stone HSDN C0023380 Lethargy C3888018 Congenital hyperinsulinism MalaCards C1313921 Urinomas C0007130 Mucinous adenocarcinoma HSDN C0000737 Abdomen pain C0020615 Hypoglycemia HSDN C0277959 Hair coarseness C2698658 Orofaciodigital syndrome type 1 MalaCards C0242936 Center pain C0042076 Urologic neoplasms HSDN C4084766 Vomiting C0013274 Patent ductus arteriosus HSDN C1549543 Administration method - pain C0006384 Bundle-branch block HSDN C4084769 Vomiting frequency C1956346 Coronary artery disease HSDN C0009080 Finger clubbing C0021368 Inflammation MalaCards C0040485 Wryneck C0038454 Cerebrovascular accident HSDN C3898969 Have been vomiting C0016510 Foot diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3469186 Hemochromatosis, type 1 HSDN C1565249 Limitation, mobility C0026613 Motor skills disorders HSDN C0000737 Abdomen pain C2981665 Stage ib distal bile duct cancer UMLS C0015938 Fetal macrosomia C0040053 Thrombosis HSDN C1963071 Back pain adverse event C0033817 Pseudomonas infections HSDN C3539020 Pelvic pain decreasing in frequency C0023903 Liver neoplasms HSDN C0454644 Delayed language development C2931294 Wiedemann grosse dibbern syndrome MalaCards C1549543 Administration method - pain C0037937 Spine injury HSDN C0020649 Blood pressure decreased C0265836 Congenital tricuspid valve stenosis MalaCards C4084769 Vomiting frequency C0006309 Brucellosis HSDN C1549543 Administration method - pain C0030421 Paraganglioma HSDN C3814874 Loss of appetite question C0043398 Yellow fever, urban MalaCards C0518090 Frequency of pain question C0040765 Transsexualism HSDN C4085317 Diarrhea frequency C0206603 Circoviridae infection HSDN C0000737 Abdomen pain C0717360 Disease lyme vaccine HSDN C1963184 Nystagmus adverse event C0265223 Cohen syndrome HPO C0030552 Paralysis partial C0014549 Tonic-clonic epilepsy HSDN C1963093 Dizziness adverse event C0017563 Gingival diseases HSDN C0030193 Sense of pain C0025517 Metabolic diseases HSDN C3887638 Failure to thrive in infant C0043208 Wolman disease HPO C4084724 Usual severity constipation C1739094 Foodborne botulism OrphaNet|MalaCards C0206146 Myocardial stunning C0021890 Intraoperative complications HSDN C1579931 Depressed - symptom C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 HPO C0518090 Frequency of pain question C0004589 B. anthracis HSDN C0151827 Pain eye C1423541 Vangl2 gene HSDN C0013362 Dysarthrias C0007766 Intracranial aneurysm HSDN C4085222 Nausea C0036239 Satiety HSDN C0497406 Over weight C0037315 Sleep apnea syndromes HSDN C0043094 Weight gain C0017601 Glaucomas HSDN C0013378 Dysgensia C0021890 Intraoperative complications HSDN C0027497 Queasy C0002871 Anemia HSDN C2029884 Hearing loss by exam C1299262 Sarcoma - category (morphologic abnormality) HSDN C0004134 Dyssynergia C0020538 Hypertensive disease HSDN C0041657 Consciousness loss C0010054 Coronary arteriosclerosis HSDN C0004093 Asthenia C0036341 Schizophrenia HSDN C1549543 Administration method - pain C0041971 Tumor urethra HSDN C0036572 Convulsion C1959620 Dihydropyrimidine dehydrogenase deficiency MalaCards|HPO|UMLS C0005745 Blepharoptosis C1840378 Brachycephalofrontonasal dysplasia OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0268141 Xeroderma pigmentosum, group g HPO C4084766 Vomiting C0016658 Fracture bone HSDN C4084725 Usual severity cough C0013808 Electroconvulsive therapy HSDN C2984057 Have nausea C0011615 Dermatitis, atopic HSDN C1963093 Dizziness adverse event C0040997 Trigeminal neuralgia HSDN C0150055 Pain chronic C0019693 Hiv infections HSDN C1963093 Dizziness adverse event C0474820 Glomerocytoma tympanicum HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037744 Perceptual spatial orientation HSDN C0026838 Spasticity muscle C0270855 Early myoclonic encephalopathy MalaCards|HPO|UMLS C0030193 Sense of pain C0000833 Abscess HSDN C0235153 Sensory hallucination C1621920 Intermediate maple syrup urine disease HPO C0030552 Paralysis partial C0018799 Heart diseases HSDN C4042891 Sleep wake disorders C0018235 Aggrieved HSDN C0033774 Skin pruritus C3272461 Ampulla of vater pancreatobiliary type adenocarcinoma UMLS C2203646 Jaundice C0023869 Lithiasis HSDN C0752210 Paroxysmal dyskinesia C1970238 Episodic kinesigenic dyskinesia 2 MalaCards C3887873 Hearing loss C0023051 Laryngeal diseases HSDN C0011206 Delirium acute C0016542 Foreign body HSDN C0022568 Inflammation corneal C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C0004134 Dyssynergia C1849085 Mousa al din al nassar syndrome OrphaNet|MalaCards C0009806 Constipate C0037397 Behavior social HSDN C1963087 Constipation adverse event C0017658 Glomerulonephritis HSDN C2984058 Have pain C1720983 Channelopathies HSDN C0023380 Lethargy C0342788 Renal carnitine transport defect MalaCards|HPO C1963184 Nystagmus adverse event C3809221 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 MalaCards C4085661 Usual severity nausea C0034065 Pulmonary embolism HSDN C0018991 Paralysis one side of body C2675211 Episodic ataxia, type 6 (disorder) MalaCards|HPO C0234523 Apraxia, classic C0175702 Williams syndrome HSDN C0023012 Delay language C3150803 Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia MalaCards|HPO C4084776 Weight loss C1854336 Paragangliomas 3 MalaCards C0018772 Deafness C0496842 Malignant neoplasm of pituitary gland MalaCards C0242936 Center pain C0020433 Hyperbilirubinemia HSDN C1963170 Hypothermia adverse event C0860603 Anxiety symptoms HSDN C0042024 Urine incontinence C0043253 Trauma blunt HSDN C1384666 Decreased hearing C1836522 Schindler disease, type ii OrphaNet|HPO|MalaCards C0043094 Weight gain C0020445 Hypercholesterolemia, familial HSDN C2132198 Abnormal blistering of the skin C0406355 Acrokeratosis paraneoplastica of bazex OrphaNet|MalaCards C0013421 Dystonia C0016510 Foot diseases HSDN C2984057 Have nausea C1962979 Burn adverse event HSDN C3274924 Have been coughing C0005779 Blood coagulation disorders HSDN C0518090 Frequency of pain question C0006261 Bronchial diseases HSDN C0040822 D tremors C1547046 Kind of quantity - taste HSDN C0007859 Pain neck C0032019 Pituitary neoplasms HSDN C0034124 Pupillary disorder C0917796 Optic atrophy, hereditary, leber HSDN C0030193 Sense of pain C0855009 Peripheral neuroepithelioma of bone UMLS C0241210 Speaking delay C0268228 Neuraminidase 1 deficiency OrphaNet C4085211 Pain distress question C0040765 Transsexualism HSDN C3815497 Cough C0037930 Spinal cord neoplasms HSDN C3815497 Cough C1455705 Pulmonary histiocytosis x OrphaNet|MalaCards C0020903 Illusion C0030974 Perceptual defense HSDN C0221263 Cafe au lait spot C0175692 Johanson-blizzard syndrome MalaCards|HPO C2237041 Shox gene with short stature C0035934 Rubinstein-taybi syndrome OrphaNet|HPO|MalaCards C0003862 Pain joint C0079173 Craniomandibular disorders HSDN C0008031 Pain chest C1709574 Pleural epithelioid mesothelioma UMLS C4085210 Usual severity pain C0011303 Demyelinating diseases HSDN C0018784 Deafness sensorineural C1861736 Spinocerebellar ataxia 31 (disorder) HPO C4084773 Bothered by weight gain C3714644 Thymus neoplasms HSDN C0030193 Sense of pain C0086957 Naffziger syndrome HSDN C0005745 Blepharoptosis C0795841 Jacobsen distal 11q deletion syndrome OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1956125 Alagille syndrome 1 HPO C0015469 Facial paralysis C0262593 Injury nerve peripheral HSDN C0017181 Gastrointestinal bleed C0242584 Autoimmune thrombocytopenia MalaCards C0277873 Nasal flaring C1866958 Laryngeal and pharyngeal hypoplasia with omphalocele MalaCards|UMLS C1384666 Decreased hearing C0017638 Glioma HSDN C4085317 Diarrhea frequency C0022650 Kidney calculi HSDN C2984058 Have pain C0017154 Gastritis, atrophic HSDN C0242936 Center pain C0024959 Maxillary sinusitis HSDN C0542476 Forgetful C1843792 Frontotemporal lobar degeneration with tdp43 inclusions, grn-related HPO C0000737 Abdomen pain C1333856 Grade 3 colorectal adenocarcinoma UMLS C4084724 Usual severity constipation C0039082 Syndrome HSDN C0751840 Pure alexia C0338437 Neurocysticercosis HSDN C0013604 Edematous C0013502 Echinococcosis HSDN C0043094 Weight gain C0016510 Foot diseases HSDN C0086439 Activity decreased C0085292 Stiff-person syndrome HSDN C0020673 Hypothermia (central) (local) C0006434 Burn injury HSDN C0973461 Dysphasia C1851708 Encephalopathy, recurrent, of childhood MalaCards C0424755 Fever symptoms C0015745 Ingestive behavior HSDN C4084726 Distress cough C3179093 Injuries, laryngeal nerve HSDN C1279888 Proteinuria of undiagnosed cause C1510460 Orofaciodigital syndrome i MalaCards|HPO C3815497 Cough C0020538 Hypertensive disease HSDN C4042834 Compassion fatigue C0033873 Psychiatry HSDN C0017181 Gastrointestinal bleed C1304456 Congo hemorrhagic fever MalaCards C0522224 Palsied C0007286 Carpal tunnel syndrome HSDN C0520909 Ponv C0007820 Cerebrovascular disorders HSDN C4084727 Cough frequency C0031903 Pigeon breeder's lung MalaCards C3146279 Coma C0017178 Gastrointestinal diseases HSDN C0011175 Deficient fluid volume C0015624 Fanconi syndrome HPO C2237041 Shox gene with short stature C2930812 Generalized elastolysis MalaCards C4084784 Diarrhea C0022758 Kap HSDN C0027498 Nausea vomiting C0265216 X-linked hydrocephalus syndrome MalaCards C3641755 Have constipation C0000768 Congenital abnormality HSDN C0023012 Delay language C1842676 Spinocerebellar ataxia, autosomal recessive 6 (disorder) MalaCards C0162834 Hyperpigmentation C0271742 Glucocorticoid deficiency with achalasia HPO C4085862 Bothered by nausea C0008073 Developmental disabilities HSDN C0043094 Weight gain C0242350 Erectile dysfunction HSDN C0151786 Weakness muscle C0153653 Malignant tumor of parathyroid gland MalaCards C0557874 Global developmental delay C0023014 Language development disorders MalaCards C0026838 Spasticity muscle C4040739 3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome MalaCards C4084776 Weight loss C0019087 Hemorrhagic disorders HSDN C0424755 Fever symptoms C0262593 Injury nerve peripheral HSDN C0037763 Spasm C0011854 Diabetes mellitus, insulin-dependent HSDN C0151889 Reflexes tendon increased C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C4084767 Bothered by vomiting C0018946 Hematoma, subdural HSDN C0004604 Pain back C1000483 Genus anemia HSDN C0151798 Liver necrosis C0279606 Childhood hepatocellular carcinoma MalaCards C0019572 Hairiness C1850155 Torg-winchester syndrome MalaCards|HPO C0426579 Anorexia symptom C0153460 Malignant neoplasm of tail of pancreas MalaCards C0015672 Decreased energy C2937421 Prostatic hyperplasia HSDN C0948992 Lower extremity paresthesia C0740728 Lower extremity problem UMLS C0522224 Palsied C0001432 Adenoma, chromophobe HSDN C0020438 Hypercalciuria C3150933 Hyperaldosteronism, familial, type iii MalaCards|HPO C0039070 Collapse fleeting C0376532 Epilepsy, rolandic HSDN C0020580 Decreased sensation C0033975 Psychotic disorders HSDN C0751093 Dystonia, limb C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) UMLS C4084802 Usual severity diarrhea C0032002 Pituitary diseases HSDN C0751188 Dural headache post puncture C0475523 Spinal+epidural anesthesia-inducd headache during pregnancy UMLS C3641755 Have constipation C1335686 Neuroendocrine neoplasm of rectum MalaCards C0018784 Deafness sensorineural C0033800 Pseudoglioma MalaCards C0002170 Alopecia disorders C0085110 Severe combined immunodeficiency OrphaNet|MalaCards C4084724 Usual severity constipation C1704272 Benign prostatic hyperplasia HSDN C2315100 Pediatric failure to thrive C1846421 Lathosterolosis OrphaNet|HPO|MalaCards C0033377 Caudal displacement C1527406 Rhizomelic pseudopolyarthritis MalaCards C0522224 Palsied C0032851 Disease poultry HSDN C0151889 Reflexes tendon increased C0574080 Guanidinoacetate methyltransferase deficiency MalaCards|HPO C2032396 Pelvic pain on the right C0041960 Ureterocele HSDN C0424755 Fever symptoms C0015408 Eye injury HSDN C2919142 Short stature adverse event C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C0026205 Pupillary constriction C1962986 Glaucoma adverse event HSDN C4085317 Diarrhea frequency C0030319 Panic disorder HSDN C0037771 Paraparesis spastic C0020255 Hydrocephalus HSDN C4084775 Usual severity weight loss C0334299 Carcinoid tumor no icd-o subtype HSDN C4084724 Usual severity constipation C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0812426 Kidney problem C0595916 Renal toxicity UMLS C0007758 Cerebellar ataxia C0020607 Hypodermyiases HSDN C4085210 Usual severity pain C0024899 Mastocytosis HSDN C0557874 Global developmental delay C1864436 Muenke syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0037274 Dermatologic disorders HSDN C0008031 Pain chest C0021831 Intestinal diseases HSDN C0030193 Sense of pain C0206637 Chondrosarcoma, mesenchymal UMLS C0151786 Weakness muscle C0011884 Diabetic retinopathy HSDN C0015970 Fever unknown origin C0002390 Extrinsic allergic alveolitis HSDN C4085210 Usual severity pain C0038016 Spondylolisthesis HSDN C0018808 Murmur C0040761 Transposition of great vessels HSDN C0018681 Headache, cephalalgia C1136043 Acoustic schwannoma, bilateral HPO C0426579 Anorexia symptom C1535917 Nipah virus infection MalaCards C4084897 Sleep disturbance subordinate domain C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C0518090 Frequency of pain question C0009782 Connective tissue diseases HSDN C0024031 Back pain lower back C0039128 Syphilis HSDN C0162298 Stiffness joints C0751918 Cockayne pelizaeus merzbacher disease MalaCards C3815497 Cough C0684249 Carcinoma of lung DiseaseOntology C0042940 Disorder of voice C0029295 Oropharyngeal neoplasms HSDN C0011991 Loose stools C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0011991 Loose stools C2004491 Cicatrix HSDN C3146279 Coma C0035126 Reperfusion injury HSDN C0019079 Bloody sputum C0037313 Sleep HSDN C0008031 Pain chest C0014866 Esophageal stenosis HSDN C0151889 Reflexes tendon increased C1539956 Tgm6 gene HPO C0000737 Abdomen pain C1513718 Mucin-producing intrahepatic cholangiocarcinoma UMLS C0426579 Anorexia symptom C1334968 Nodular lymphocyte predominant hodgkin lymphoma MalaCards C0013362 Dysarthrias C1846564 Spastic paraplegia 7, autosomal recessive MalaCards|HPO C0454644 Delayed language development C3266843 47, xyy syndrome OrphaNet C4085548 Usual severity dizziness C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C0242936 Center pain C0015625 Fanconi anemia HSDN C0030193 Sense of pain C0343266 Algodystrophy of knee UMLS C1963184 Nystagmus adverse event C1848554 Methylmalonic aciduria, cbld type, variant 2 HPO C0036572 Convulsion C0027773 Nesidioblastosis HSDN C0040485 Wryneck C0015464 Facial nerve diseases HSDN C0020505 Excessive eating C0860549 Refeed syndrome HSDN C4084766 Vomiting C1839530 Valproate sensitivity HPO C0020455 Hypergammaglobulinemia C0027707 Nephritis, interstitial HSDN C0015230 Exanthem C0040262 Tinea versicolor UMLS C4084724 Usual severity constipation C0036677 Sensory threshold HSDN C1963091 Diarrhea adverse event C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0018777 Deafness, conductive C0029899 Otosclerosis MalaCards C4085661 Usual severity nausea C0037929 Spinal cord injuries HSDN C0152227 Tearing excessive C0334299 Carcinoid tumor no icd-o subtype MalaCards C0000727 Abdomen acute C0542241 Toxemia bacterial HSDN C1963091 Diarrhea adverse event C0029443 Osteomyelitis HSDN C0000737 Abdomen pain C0751544 Tangier disease neuropathy MalaCards C2024878 Cardiovascular surgery result: dyspnea C1563716 Thyroid dysgenesis HSDN C1549543 Administration method - pain C0018946 Hematoma, subdural HSDN C0013404 Respiratory difficulty C0018800 Cardiomegaly HSDN C4084775 Usual severity weight loss C0009373 Colonic diseases HSDN C0574992 Finger joint laxity C1855175 Metaphyseal dysostosis, mental retardation, and conductive deafness MalaCards|UMLS C0018784 Deafness sensorineural C2930866 Ramos arroyo clark syndrome MalaCards C0042384 Vasculitis, nonspecific C0406817 Collagenoma, familial cutaneous MalaCards C0242936 Center pain C1509147 Histiocytoma HSDN C0018772 Deafness C0033595 Prostitution HSDN C2911647 Weight gain adverse event C0027627 Neoplasm metastasis HSDN C1549543 Administration method - pain C0014556 Epilepsy, temporal lobe HSDN C1836296 Lower extremity weakness C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO|UMLS C4084784 Diarrhea C2242987 Benign mastocytoma MalaCards C0030486 Extremity paralysis, lower C0860603 Anxiety symptoms HSDN C0042571 Vertigo subjective C0086543 Cataract nos HSDN C1963154 Renal failure adverse event C0268425 Alstrom syndrome MalaCards C0026821 Cramp C1553188 Hemolysis - observation HSDN C0151786 Weakness muscle C0009373 Colonic diseases HSDN C0028738 Nystagmus C2931074 Cone rod dystrophy amelogenesis imperfecta OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C0265449 Pallister-killian syndrome OrphaNet|MalaCards C0009676 Confusion state C0751815 Carotid artery, internal, dissection HSDN C0037763 Spasm C0017601 Glaucomas HSDN C0003862 Pain joint C2749759 Macrothrombocytopenia-stomatocytosis, mediterranean HPO C0424755 Fever symptoms C0023283 Leishmaniasis, cutaneous HSDN C0033774 Skin pruritus C0040558 Toxoplasmosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206681 Adenocarcinoma, clear cell HSDN C3641756 Have diarrhea C0026269 Mitral valve stenosis HSDN C0003550 Broca aphasia C0236969 Substance-related disorders HSDN C0426579 Anorexia symptom C0220847 C hepatitis virus HSDN C4084769 Vomiting frequency C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0026636 Mouth diseases HSDN C1963093 Dizziness adverse event C0003850 Arteriosclerosis HSDN C3808046 Breathing dysregulation C0020681 Sleep-related respiratory failure MalaCards C0577567 Mass of urogenital structure C0473229 Perirenal and periureteric post-transplant lymphocele UMLS C2242996 Tingling C0027819 Neuroblastoma HSDN C0030794 Pelvis pain C2586211 Thrombosis of blood vessel HSDN C0497406 Over weight C0024115 Lung diseases HSDN C3146279 Coma C0038819 Siriasis HSDN C4084802 Usual severity diarrhea C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C3898969 Have been vomiting C1970820 Fabry disease, cardiac variant HPO C4085210 Usual severity pain C0003860 Arteritis HSDN C0037771 Paraparesis spastic C0086795 Pfaundler-hurler syndrome HPO C0349489 Fetal hypoxia C0015959 Fetomaternal bleeding HSDN C0522224 Palsied C0040412 Fissured tongue HSDN C1963063 Anorexia adverse event C0032914 Pre-eclampsia HSDN C0151889 Reflexes tendon increased C1862441 Ataxia, spastic, with congenital miosis OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0034929 Reflex HSDN C0000737 Abdomen pain C0033873 Psychiatry HSDN C0034151 Hyperglobulinemic purpura C0009326 Collagen diseases HSDN C0000727 Abdomen acute C0043410 Pseudotuberculosis HSDN C2237041 Shox gene with short stature C1842082 Vater-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency OrphaNet|MalaCards C4084769 Vomiting frequency C0037313 Sleep HSDN C0221752 Rbc urine C0022739 Klippel-trenaunay-weber syndrome MalaCards C0015230 Exanthem C0276244 Equine coital exanthema UMLS C2237041 Shox gene with short stature C2930900 Beta-sarcoglycanopathy MalaCards C4084768 Usual severity vomiting C0036095 Salivary gland neoplasms HSDN C2237041 Shox gene with short stature C0268140 Xeroderma pigmentosum, group f HPO C4085317 Diarrhea frequency C0023364 Leptospirosis HSDN C0231471 Posture abnormality C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO C0917816 Deficiency mental C2713347 7-dehydrocholesterol reductase deficiency OrphaNet|HPO|MalaCards C0015230 Exanthem C0275747 Erythematous plaques of carate UMLS C4085549 Dizziness C0002726 Amyloidosis HSDN C3665346 Loss sight C1846980 Senior-loken syndrome 3 MalaCards C3463815 Feel fatigue C0334511 Pleural solitary fibrous tumor HSDN C4084774 Have weight loss C0001584 Adolescent psychology HSDN C1263846 Attention deficit disorder with hyperactivity C0544012 Aberfeld's syndrome MalaCards C2984057 Have nausea C1258215 Ileus HSDN C0042798 Vision dim C0023521 Globoid cell leukodystrophy OrphaNet C3463815 Feel fatigue C0000833 Abscess HSDN C0522224 Palsied C0028758 Bonding HSDN C1959630 Eye pain adverse event C2616767 Mycetoma HSDN C0234144 Dysgraphia C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0033774 Skin pruritus C0001418 Adenocarcinoma HSDN C0023012 Delay language C3150923 Mental retardation with language impairment and autistic features HPO C0042571 Vertigo subjective C1857333 Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia OrphaNet|MalaCards C4084766 Vomiting C0043168 Whooping cough due to unspecified organism HSDN C0004134 Dyssynergia C2678048 Spinocerebellar ataxia, x-linked 5 MalaCards|UMLS C0042928 Paralysis vocal cord C0040587 Mounier kuhn syndrome HSDN C0015672 Decreased energy C3150750 Agammaglobulinemia 2, autosomal recessive MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0948039 Bacterial gastritis MalaCards C2984058 Have pain C0028431 Acquired nasal deformities HSDN C0413252 Hypothermia due to exposure C0039128 Syphilis HSDN C1962956 Flatulence adverse event C0020538 Hypertensive disease HSDN C1962972 Proteinuria adverse event C0241158 Cicatrix skin HSDN C0233514 Behavior abnormal C0024748 Alpha-mannosidosis OrphaNet C0012833 Dizzy C3827868 Tachycardia by ecg finding HSDN C1963249 Tinnitus adverse event C1845095 Deafness, x-linked 5 (disorder) MalaCards|HPO C4084784 Diarrhea C0035923 German measles vaccine HSDN C0016199 Pain flank C0678053 Adrenocortical carcinoma, metastatic UMLS C0023015 Language handicap C0002989 Epithelioid hemangioma of skin HSDN C4085210 Usual severity pain C0477611 Spin osteochondrosis, unsp HSDN C0040485 Wryneck C0027643 Neoplasm recurrence, local HSDN C0000737 Abdomen pain C0005779 Blood coagulation disorders HSDN C0036572 Convulsion C0039128 Syphilis HSDN C0011991 Loose stools C0034888 Rectal prolapse HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010635 Cystadenoma, mucinous HSDN C0009806 Constipate C0033578 Prostatic neoplasms HSDN C4084802 Usual severity diarrhea C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C0156317 Genital edema male C0554315 Other male genital dis. nos UMLS C0497247 Blood pressure elevation C0029455 Osteopoikilosis (disorder) MalaCards C1384666 Decreased hearing C0161408 Cranial nerve vii injuries HSDN C0518090 Frequency of pain question C0042995 Vulvar neoplasms HSDN C2919142 Short stature adverse event C0917715 Hajdu-cheney syndrome OrphaNet|HPO|MalaCards C3898969 Have been vomiting C0026598 Movement perception HSDN C2984057 Have nausea C0270858 Abdominal migraines MalaCards C1263846 Attention deficit disorder with hyperactivity C0398791 Nijmegen breakage syndrome OrphaNet|HPO|MalaCards C0151827 Pain eye C0043121 Wernicke encephalopathy HSDN C0011991 Loose stools C0016667 Fragile x syndrome HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0022116 Ischemia HSDN C2315100 Pediatric failure to thrive C1849236 Severe combined immunodeficiency, atypical HPO C0030552 Paralysis partial C0270707 Kluver-bucy syndrome HSDN C3829611 Nausea frequency C0029882 Otitis media HSDN C0015300 Ocular proptosis C1851710 Lateral meningocele syndrome MalaCards C2096293 Ent surgical result ear vertigo C0025149 Medulloblastoma MalaCards C0002962 Angina C0017601 Glaucomas HSDN C2984058 Have pain C0003794 Arm injury HSDN C0030193 Sense of pain C0023794 Lipoidosis HSDN C3203358 Alveolar hypoventilation C2984299 Asthma pathway HSDN C0018681 Headache, cephalalgia C0042510 Ventricular fibrillation HSDN C0427055 Face weakness C1851399 Facial palsy, familial recurrent peripheral MalaCards C0020673 Hypothermia (central) (local) C0007789 Cerebral palsy HSDN C0518090 Frequency of pain question C0019066 Nontraumatic hemoperitoneum HSDN C0030232 Color loss C3151519 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 MalaCards|HPO C4084725 Usual severity cough C0518449 Control of hip fracture risk HSDN C0241137 Skin pallor C0265428 9p+ syndrome MalaCards C0002962 Angina C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0149793 Transient monocular blindness C2930957 Hantavirosis MalaCards C0000737 Abdomen pain C0006114 Cerebral edema HSDN C0038002 Spleen enlargement C0014356 Enterocolitis MalaCards C0009676 Confusion state C2931384 Moyamoya disease 1 HSDN C0015469 Facial paralysis C0041327 Tuberculosis, pulmonary HSDN C4084802 Usual severity diarrhea C1552962 Units of measure - pica HSDN C0151827 Pain eye C0030469 Paranasal sinus diseases HSDN C0004134 Dyssynergia C4225355 Spinocerebellar ataxia, autosomal recessive 20 UMLS C4084788 Have dizziness C0016470 Food allergy HSDN C0015230 Exanthem C0037274 Dermatologic disorders UMLS C4084784 Diarrhea C0020522 Delayed hypersensitivity HSDN C0242936 Center pain C1135957 Narrative HSDN C0028738 Nystagmus C0265235 Marshall syndrome MalaCards|HPO C4084788 Have dizziness C0037305 Neoplasm, skull HSDN C1069915 Vertigo C0017638 Glioma HSDN C0234146 Absent reflex C0520720 Cyst nerve root MalaCards C0424755 Fever symptoms C0010278 Craniosynostosis HSDN C3641755 Have constipation C0034040 Puerperal disorders HSDN C0344315 Mood depressed C0017689 Glucagonoma MalaCards C0018524 Hallucinate C0017612 Glaucoma, open-angle HSDN C1962972 Proteinuria adverse event C0003467 Anxiety HSDN C0015402 Hemorrhage eye C3853779 Neonatal alloimmune thrombocytopenia HSDN C0007758 Cerebellar ataxia C0004610 Bacteremia HSDN C0006370 Bulimia C0033046 Premenstrual syndrome HSDN C4085548 Usual severity dizziness C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C0030554 Abnormal sensation C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0018524 Hallucinate C3541306 Plasmodium measurement HSDN C0003550 Broca aphasia C0003827 Art therapies HSDN C0008031 Pain chest C1850635 Atrial myxoma, familial MalaCards C0019079 Bloody sputum C2930957 Hantavirosis MalaCards C4084776 Weight loss C0525042 Feeding and eating disorders of childhood HSDN C0015672 Decreased energy C0018099 Gout HSDN C0019079 Bloody sputum C0023055 Laryngeal neoplasm HSDN C0028738 Nystagmus C1845407 Cone-rod dystrophy, x-linked, 3 HPO C0026858 Musculoskeletal pain C0009244 Behavioral cognitive therapy HSDN C1963281 Vomiting adverse event C0019270 Hernia HSDN C0030193 Sense of pain C1527311 Brain edema HSDN C1963091 Diarrhea adverse event C0011389 Dental plaque HSDN C3274924 Have been coughing C0243026 Sepsis HSDN C0151798 Liver necrosis C0024586 Malignant carcinoid syndrome MalaCards C0395923 Multisensory dizziness C0271487 Vertiginous disorder UMLS C4085549 Dizziness C0344315 Depressed mood HSDN C0243026 Generalized infection C1801959 Histiocytic medullary reticulosis (disorder) MalaCards C0035078 Failure kidney C1628319 Lattice corneal dystrophy type ii MalaCards|HPO C3665492 Pigmentations C2713443 Familial intestinal polyposis MalaCards C0030552 Paralysis partial C2240378 Cleft palate on exam HSDN C3274924 Have been coughing C1706004 Anhydrotic ectodermal dysplasias OrphaNet|MalaCards C0038506 Stutter C2936636 Anticipation, psychological HSDN C0011991 Loose stools C0009377 Colon nos pseudo obstruction HSDN C3815497 Cough C0016658 Fracture bone HSDN C4084767 Bothered by vomiting C0031212 Personality disorders HSDN C2984058 Have pain C0011880 Diabetic ketoacidosis HSDN C0042963 Symptoms vomiting C0042164 Uveitis HSDN C4084776 Weight loss C0010606 Adenoid cystic carcinoma HSDN C0850758 Pain pelvic C0002871 Anemia HSDN C2029884 Hearing loss by exam C1552262 Nurse practitioner - family HSDN C0018926 Emesis bloody C0025064 Mediastinitis HSDN C0521634 Female genital itching C3838725 Disorder of female perineum UMLS C4084788 Have dizziness C0016053 Fibromyalgia HSDN C0011991 Loose stools C0035222 Respiratory distress syndrome, adult HSDN C0221166 Paraparesis C0041295 Tuberculoma HSDN C0035229 Respiratory function impaired C0206743 Rhabdoid tumor OrphaNet|MalaCards C2984058 Have pain C1552262 Nurse practitioner - family HSDN C1962972 Proteinuria adverse event C0027743 Nerve compression syndrome HSDN C4084766 Vomiting C0919267 Ovarian neoplasm HSDN C0751837 Gait ataxic C4225289 Epilepsy, progressive myoclonic, 9 UMLS C4084784 Diarrhea C0032897 Prader-willi syndrome HSDN C0013421 Dystonia C0751870 Heredodegenerative disorders, nervous system HSDN C0086439 Activity decreased C0410203 X-linked centronuclear myopathy HPO C0022346 Yellow skin C0025637 Methemoglobinemia HSDN C0557874 Global developmental delay C1846816 Congenital disorder of glycosylation, type iiid MalaCards|HPO C2984058 Have pain C0238190 Inclusion body myositis (disorder) HSDN C0005745 Blepharoptosis C1850746 Carey-fineman-ziter syndrome OrphaNet C0522224 Palsied C0034628 Radius fracture HSDN C1963170 Hypothermia adverse event C1956346 Coronary artery disease HSDN C4085548 Usual severity dizziness C0009375 Colonic neoplasms HSDN C0150055 Pain chronic C0004096 Asthma HSDN C1963065 Apnea adverse event C0017181 Gastrointestinal hemorrhage HSDN C4084897 Sleep disturbance subordinate domain C2931857 Double cortex MalaCards C4084788 Have dizziness C0027686 Pathologic neovascularization HSDN C2024878 Cardiovascular surgery result: dyspnea C0027819 Neuroblastoma HSDN C4042891 Sleep wake disorders C0004610 Bacteremia HSDN C1963071 Back pain adverse event C0035410 Rhabdomyolysis HSDN C3539895 Pelvic pain occurs with bowel movement C0023895 Liver diseases HSDN C4085211 Pain distress question C0243010 Viral encephalitis HSDN C0917816 Deficiency mental C2936786 Aqueductal stenosis MalaCards C0727671 Red cross toothache drops C0040427 Tooth abnormalities HSDN C0426579 Anorexia symptom C0023903 Liver neoplasms MalaCards C0851578 Disorder sleep C0008625 Chromosome aberrations HSDN C1384666 Decreased hearing C1842687 Pontocerebellar hypoplasia type 3 (disorder) MalaCards|HPO C4084767 Bothered by vomiting C0001118 Acid base imbalance HSDN C0015469 Facial paralysis C1962986 Glaucoma adverse event HSDN C4084784 Diarrhea C1962958 Hematoma adverse event HSDN C0151786 Weakness muscle C0011127 Pressure ulcer HSDN C4085210 Usual severity pain C0751931 Femoral lesion nerve HSDN C2073625 X-ray of chest: pleural effusion C1969419 Pancreatitis, chronic, susceptibility to HPO C3665346 Loss sight C1849437 Mainzer-saldino disease MalaCards|HPO|UMLS C4084769 Vomiting frequency C0269291 Pregnancy heterotopic HSDN C0751495 Seizure focal C0220669 Familial benign neonatal epilepsy MalaCards|UMLS C3641755 Have constipation C0004623 Bacterial infections HSDN C0027796 Neuralgias C0007682 Cns disorder HSDN C4084774 Have weight loss C0041312 Tuberculosis git nos DiseaseOntology|HSDN|MalaCards C3274924 Have been coughing C0025284 Meningeal neoplasms HSDN C0086565 Liver function abnormal C0205710 Alpers syndrome (disorder) MalaCards|HPO C0003962 Ascites C0206624 Hepatoblastoma MalaCards C4084776 Weight loss C0027743 Nerve compression syndrome HSDN C0007398 Catatonic C0030568 Parkinsonism, postencephalitic HSDN C0042963 Symptoms vomiting C0149931 Migraine disorders MalaCards C2919142 Short stature adverse event C2675861 Lipodystrophy, congenital generalized, type 3 MalaCards|HPO C0016199 Pain flank C0877172 Hematoma, epidural, spinal HSDN C0008031 Pain chest C0039590 Testicular neoplasms HSDN C1963065 Apnea adverse event C0700639 Pyloric stenosis, hypertrophic HSDN C3887638 Failure to thrive in infant C4078861 Non ketotic hyperglycinemia syndrome MalaCards C0007758 Cerebellar ataxia C1836287 Cerebrorenodigital syndrome with limb malformations and triradiate acetabula OrphaNet|MalaCards C0542476 Forgetful C0878682 Ceruloplasmin deficiency MalaCards|HPO C4084768 Usual severity vomiting C0014549 Tonic-clonic epilepsy HSDN C0018784 Deafness sensorineural C1291386 D-glycericacidemia MalaCards|HPO C4085211 Pain distress question C0178282 Hernia of abdominal cavity HSDN C4085862 Bothered by nausea C1856401 Etfa deficiencies HPO C4084774 Have weight loss C0037361 Olfactory sense HSDN C0027497 Queasy C0393735 Headache disorders HSDN C0027497 Queasy C0015934 Fetal growth retardation HSDN C0014089 Functional encopresis C0001726 Affective symptoms HSDN C0027066 Myoclonic jerking C1846492 Spinocerebellar ataxia, autosomal recessive 4 MalaCards|UMLS C1565249 Limitation, mobility C0011854 Diabetes mellitus, insulin-dependent HSDN C0030486 Extremity paralysis, lower C0007786 Brain ischemia HSDN C0003811 Cardiac rhythm disturbance C0036421 Systemic scleroderma MalaCards C2984058 Have pain C1704421 Skin pigmentation disorder HSDN C4084769 Vomiting frequency C0032319 Pneumopericardium HSDN C0036572 Convulsion C0024961 Injuries maxillofacial HSDN C0037384 Snore C0010068 Coronary heart disease HSDN C0241137 Skin pallor C0795830 Chromosome 9p deletion syndrome MalaCards C0518090 Frequency of pain question C0042850 Vitamin b deficiency HSDN C0042963 Symptoms vomiting C0029118 Opportunistic infections HSDN C1971624 Appetite absent C0036601 Self mutilation HSDN C0010200 Cough symptom C0001721 Emotional affect HSDN C0042798 Vision dim C0022336 Creutzfeldt-jakob disease MalaCards|HPO C4085210 Usual severity pain C0029417 Osteoblastoma HSDN C3541349 Syncope C0019372 Herpesviridae infections HSDN C0242936 Center pain C0015806 Femur neck fracture HSDN C4084802 Usual severity diarrhea C0035358 Retroperitoneal neoplasm HSDN C0030552 Paralysis partial C0432215 Progressive pseudorheumatoid dysplasia HPO C2032395 Pelvic pain on the left C0037313 Sleep HSDN C0036572 Convulsion C0265306 Greig cephalopolysyndactyly syndrome MalaCards|HPO C3665492 Pigmentations C0279680 Transitional cell carcinoma of bladder MalaCards C0022346 Yellow skin C0019158 Hepatitis UMLS C3887873 Hearing loss C1269683 Major depressive disorder HSDN C4084767 Bothered by vomiting C0011265 Presenile dementia HSDN C1836296 Lower extremity weakness C1853251 Spastic paraplegia 33, autosomal dominant MalaCards|HPO|UMLS C0032617 High urine output C0010481 Cushing syndrome HSDN C3815497 Cough C0002989 Epithelioid hemangioma of skin HSDN C0497406 Over weight C0005695 Bladder neoplasm HSDN C0235299 Abdomen ruq pain C0740613 Abdomen ruq mass UMLS C2024893 Cardiovascular surgery result: fatigue C0013595 Eczema HSDN C0015469 Facial paralysis C1969106 Osteopetrosis, autosomal recessive 4 MalaCards|HPO C0751837 Gait ataxic C0521542 Brainstem infarct HSDN C0030193 Sense of pain C0007774 Cerebral arterial diseases HSDN C1963063 Anorexia adverse event C0036946 Sheep--diseases HSDN C3274924 Have been coughing C0035956 Rupture spontaneous HSDN C0012569 Double vision C0460137 Push down or depress HSDN C1963180 Neck pain adverse event C1546533 Specimen source codes - abscess HSDN C0152116 Torticollis spasmodic C3538999 Dystonia 23 MalaCards C0242936 Center pain C0041328 Renal tuberculosis HSDN C0004134 Dyssynergia C0027051 Myocardial infarction HSDN C0242936 Center pain C1328252 Mucocutaneous leishmaniasis HSDN C3539891 Pelvic pain to the rear C0016548 Foreign body migration HSDN C1963184 Nystagmus adverse event C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C0013395 Indigestion C0022661 Kidney failure, chronic HSDN C3203358 Alveolar hypoventilation C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0040822 D tremors C4225305 Leukodystrophy, hypomyelinating, 11 UMLS C2911645 Weight loss adverse event C0002170 Alopecia HSDN C4084776 Weight loss C0003469 Anxiety disorders HSDN C3539020 Pelvic pain decreasing in frequency C0038941 Incisional infection HSDN C1963064 Anxiety adverse event C0035934 Rubinstein-taybi syndrome OrphaNet|MalaCards C3641756 Have diarrhea C0241158 Cicatrix skin HSDN C0039070 Collapse fleeting C0034372 Quadriplegia UMLS C2024893 Cardiovascular surgery result: fatigue C0023798 Lipoma HSDN C4084784 Diarrhea C0006271 Bronchiolitis HSDN C3898969 Have been vomiting C0039980 Chest injury HSDN C0026826 High muscle tone C0268581 Holocarboxylase synthetase deficiency MalaCards|HPO C4085661 Usual severity nausea C0033046 Premenstrual syndrome HSDN C1963170 Hypothermia adverse event C0027809 Neurilemmoma HSDN C1963091 Diarrhea adverse event C2242987 Benign mastocytoma MalaCards C0042571 Vertigo subjective C0022701 Kinesthesia HSDN C0009806 Constipate C3495422 Finding relating to sexuality and sexual activity HSDN C2029884 Hearing loss by exam C0026636 Mouth diseases HSDN C1963087 Constipation adverse event C1848519 Waardenburg syndrome, type 4a OrphaNet|HPO|MalaCards C3539023 Pelvic pain increasing in frequency C0018199 Granuloma, plasma cell HSDN C2024878 Cardiovascular surgery result: dyspnea C0041956 Ureteral obstruction HSDN C4084726 Distress cough C0025060 Mediastinal cyst HSDN C4085210 Usual severity pain C0023269 Leiomyosarcoma HSDN C2984058 Have pain C0022423 Judgement HSDN C2237041 Shox gene with short stature C1851996 Dwarfism tall vertebrae OrphaNet|HPO C0002962 Angina C0031036 Polyarteritis nodosa HSDN C0426579 Anorexia symptom C0036224 Sarcoma, yoshida HSDN C0015402 Hemorrhage eye C0162869 Aneurysm, ruptured HSDN C1961131 Cough adverse event C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0917816 Deficiency mental C0036391 Schwartz-jampel syndrome OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0559260 Congenital scoliosis HSDN C0023012 Delay language C2751651 Chromosome 19q13.11 deletion syndrome OrphaNet|MalaCards C0600142 Flash hot C1552052 Religious affiliation - meditation HSDN C0008031 Pain chest C1851124 Desmoid disease, hereditary MalaCards C1971624 Appetite absent C0040136 Thyroid neoplasm HSDN C0751837 Gait ataxic C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0085636 Light sensitivity C1857395 De toni-debre-fanconi syndrome HSDN|HPO C1963281 Vomiting adverse event C1856401 Etfa deficiencies HPO C0036572 Convulsion C0034068 Pulmonary eosinophilia HSDN C0027796 Neuralgias C0017181 Gastrointestinal hemorrhage HSDN C0036572 Convulsion C0001529 Dercum disease MalaCards C0018991 Paralysis one side of body C0020255 Hydrocephalus HSDN C4020887 Photodysphoria C0035334 Retinitis pigmentosa OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0012691 Dislocations HSDN C0028081 Night sweat C0334630 Hodgk,nod scl,lymph depletn UMLS C1069915 Vertigo C0018800 Cardiomegaly HSDN C3641756 Have diarrhea C1257915 Intestinal polyposis HSDN C4085317 Diarrhea frequency C0023886 Liver abscess, amebic HSDN C2984058 Have pain C0038363 Aphthous stomatitis HSDN C0010520 Skin cyanosis C0175704 Leopard syndrome HSDN C0917801 Sleep disorder insomnia C1960036 Psychophysiologic insomnia UMLS C0013421 Dystonia C0859897 Cord dysfunction vocal HSDN C0000737 Abdomen pain C0039231 Tachycardia HSDN|UMLS C4049644 Depression C0023788 Whipple disease OrphaNet|MalaCards C0151786 Weakness muscle C0016719 Friedreich ataxia OrphaNet|HPO C0009421 Comatose C0034065 Pulmonary embolism HSDN C4084767 Bothered by vomiting C1855109 Methylmalonic aciduria cbla type HPO C0497247 Blood pressure elevation C1836327 Rhabdoid tumor predisposition syndrome 1 (disorder) MalaCards C4042891 Sleep wake disorders C0997768 Glaucoma HSDN C0242936 Center pain C1555865 Forensic psychiatry HSDN C2984058 Have pain C0041601 Ulna fracture HSDN C4084775 Usual severity weight loss C0018809 Heart neoplasm HSDN C0152169 Colic renal C0013922 Embolism HSDN C1069915 Vertigo C0037369 Smoking HSDN C0042798 Vision dim C0268494 Oculocutaneous albinism type 1 MalaCards|HPO C4084773 Bothered by weight gain C1962986 Glaucoma adverse event HSDN C0010520 Skin cyanosis C0007137 Squamous cell carcinoma HSDN C0042571 Vertigo subjective C0040046 Thrombophlebitis HSDN C0427055 Face weakness C4014814 Myopathy, centronuclear, 5 UMLS C0000737 Abdomen pain C1335315 Pancreatic serous cystadenocarcinoma UMLS C0018777 Deafness, conductive C0027858 Neuroma HSDN C0043094 Weight gain C0014866 Esophageal stenosis HSDN C0033377 Caudal displacement C0265248 Ruvalcaba syndrome OrphaNet|MalaCards C4085661 Usual severity nausea C0010340 Critical illness HSDN C0002962 Angina C0021228 Variability of individual responses HSDN C0349588 Stature short C0920349 Sponastrime MalaCards C0015672 Decreased energy C0017168 Gastroesophageal reflux disease HSDN C0026838 Spasticity muscle C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4085317 Diarrhea frequency C0015393 Eye abnormalities HSDN C0018784 Deafness sensorineural C1863752 Enlarged vestibular aqueduct HPO C4084776 Weight loss C2931638 Chromosome 8, monosomy 8p23 1 MalaCards C2984058 Have pain C0016724 Froehlich's syndrome HSDN C0026884 Muteness C0039792 Psychotherapeutic interaction HSDN C2024878 Cardiovascular surgery result: dyspnea C0029463 Osteosarcoma HSDN C0917816 Deficiency mental C2674937 Chromosome 10q26 deletion syndrome MalaCards C0027066 Myoclonic jerking C1843015 Alzheimer disease, familial, 3, with spastic paraparesis and apraxia HPO C4084766 Vomiting C3665596 Warts HSDN C0027796 Neuralgias C0020255 Hydrocephalus HSDN C3829611 Nausea frequency C3814778 Hemolytic index HSDN C1963281 Vomiting adverse event C0033968 Psychotherapeutic technique HSDN C2984058 Have pain C0877149 Pain patellofemoral syndrome HSDN C0028961 Urine output decreased C0019021 Hemoglobin c disease HSDN C0522224 Palsied C0162871 Aortic aneurysm, abdominal HSDN C1963281 Vomiting adverse event C0027022 Myeloproliferative disease HSDN C0030193 Sense of pain C0198632 Pneumoperitoneum HSDN C0037763 Spasm C0017185 Gastrointestinal neoplasms HSDN C0036572 Convulsion C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO|UMLS C4085862 Bothered by nausea C0520679 Sleep apnea, obstructive HSDN C0013404 Respiratory difficulty C2609414 Acute kidney injury HSDN C0557874 Global developmental delay C3150939 Beaulieu-boycott-innes syndrome MalaCards|HPO C4085661 Usual severity nausea C0342443 Adrenal cushing's syndrome HSDN C2315100 Pediatric failure to thrive C2931242 Familial waldmann's disease MalaCards C2029884 Hearing loss by exam C0008924 Cleft lip HSDN C1557397 Adverse event associated with pain C0030922 Peptic ulcer hemorrhage HSDN C1963093 Dizziness adverse event C0242698 Ventricular dysfunction, left HSDN C0917816 Deficiency mental C0268126 Adenylosuccinate lyase deficiency (disorder) OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C0018036 Hypertension, goldblatt OrphaNet C0007758 Cerebellar ataxia C1412749 Bbs4 gene HPO C2024893 Cardiovascular surgery result: fatigue C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C1838869 Proximal neurogenic muscle weakness C0553604 Myotonic disorders MalaCards C2315100 Pediatric failure to thrive C0037769 West syndrome HSDN C4085317 Diarrhea frequency C0032019 Pituitary neoplasms HSDN C0040034 Thrombocytopenia C3151209 Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome HPO C4085211 Pain distress question C3146297 Study of behavior during childhood HSDN C3887638 Failure to thrive in infant C3472585 Congenital monosaccharide malabsorption MalaCards C0018772 Deafness C0032371 Poliomyelitis HSDN C4020887 Photodysphoria C0017609 Glaucoma, neovascular OrphaNet|MalaCards C4085549 Dizziness C0340493 Paroxysmal familial ventricular fibrillation MalaCards C4085210 Usual severity pain C0017154 Gastritis, atrophic HSDN C2024878 Cardiovascular surgery result: dyspnea C0271865 Autoimmune hypoparathyroidism MalaCards C2984058 Have pain C0553980 Endomyocardial fibrosis HSDN C0010520 Skin cyanosis C0023569 Levocardia HSDN C0036659 Sensation disorder C0022104 Irritable bowel syndrome HSDN C1549543 Administration method - pain C0005119 Bereavement HSDN C0035078 Failure kidney C0033847 Pseudoxanthoma elasticum MalaCards|HPO C0424755 Fever symptoms C0206701 Cystadenocarcinoma, serous HSDN C0036572 Convulsion C0013364 Dysautonomia, familial HPO C0026838 Spasticity muscle C0262655 Recurrent urinary tract infection HSDN C3665347 Vision impaired C0339510 Vitelliform macular dystrophy OrphaNet|HPO|MalaCards C0009806 Constipate C2981398 Stage iia colorectal cancer UMLS C0036396 Sciatica C0085222 Psoas muscle abscess HSDN C2237041 Shox gene with short stature C2750732 Noonan syndrome 6 MalaCards|HPO C4084726 Distress cough C0494491 Mononeuropathies HSDN C0151740 Intracranial hypertension C0010273 Craniofacial dysostosis MalaCards C1963093 Dizziness adverse event C3554047 Ventricular tachycardia, catecholaminergic polymorphic, 4 MalaCards C1963180 Neck pain adverse event C3813607 Infantile gastroesophageal reflux HSDN C0850758 Pain pelvic C0438692 Vaginal discharge symptom HSDN C0270948 Neurogenic muscular atrophy C0271689 Insulin receptor, defect in HPO C0033774 Skin pruritus C0005398 Cholestasis, extrahepatic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242550 Behavior, risk reduction HSDN C0018784 Deafness sensorineural C0013182 Drug allergy HSDN C0011175 Deficient fluid volume C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0234518 Speech slurred C0242287 Isaacs syndrome HPO C4084775 Usual severity weight loss C2749485 Nblst1 HPO C0034155 Thrombotic thrombocytopenic purpura C0035305 Retinal detachment HSDN C3887873 Hearing loss C0796121 Primrose syndrome MalaCards C4084784 Diarrhea C0268312 Progressive intrahepatic cholestasis (disorder) HPO C0917816 Deficiency mental C3150999 Chromosome 7q11.23 deletion syndrome, distal, 1.2-mb MalaCards C0270948 Neurogenic muscular atrophy C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C0018681 Headache, cephalalgia C0162871 Aortic aneurysm, abdominal HSDN C2096293 Ent surgical result ear vertigo C0022665 Kidney neoplasm HSDN C4084773 Bothered by weight gain C0037929 Spinal cord injuries HSDN C1963091 Diarrhea adverse event C0018923 Hemangiosarcoma HSDN C0000727 Abdomen acute C0206633 Angiomyolipoma HSDN C0036572 Convulsion C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C4085210 Usual severity pain C1412004 Tumor of the pineal region HSDN C0013604 Edematous C0162425 Intent HSDN C0018926 Emesis bloody C0013292 Obstruction duodenal HSDN C1557397 Adverse event associated with pain C0162429 Malnutrition HSDN C1962957 Flushing adverse event C0025063 Mediastinal neoplasms HSDN C0038868 Supranuclear palsy progressive C0027849 Neuroleptic malignant syndrome HSDN C1860844 Sparse, thin hair C1837756 Mandibuloacral dysplasia with type b lipodystrophy MalaCards|HPO C4085210 Usual severity pain C0005935 Bone conduction HSDN C0426579 Anorexia symptom C0017689 Glucagonoma OrphaNet|MalaCards C0575081 Abnormal gait C0019562 Von hippel-lindau syndrome OrphaNet|HPO|MalaCards C1963180 Neck pain adverse event C0003872 Arthritis, psoriatic HSDN C0030193 Sense of pain C0042063 Urogenital abnormalities HSDN C0037763 Spasm C0004936 Mental disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0276926 Schistosoma hematobium infection HSDN C1557397 Adverse event associated with pain C0041960 Ureterocele HSDN C0018772 Deafness C0236736 Cocaine-related disorders HSDN C1963093 Dizziness adverse event C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) MalaCards C0270948 Neurogenic muscular atrophy C1850568 Nakajo syndrome MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0004099 Asthma, exercise-induced HSDN C2237041 Shox gene with short stature C3179239 Osteopetrosis autosomal dominant type 2 OrphaNet|HPO|MalaCards C0018772 Deafness C0796147 Acrocallosal syndrome MalaCards|HPO C3641756 Have diarrhea C0086543 Cataract nos HSDN C4084784 Diarrhea C3280314 Combined malonic and methylmalonic aciduria MalaCards C0024031 Back pain lower back C0078981 Arachnoid cysts HSDN C0004604 Pain back C1997249 Neuralgia, pudendal MalaCards C4084775 Usual severity weight loss C0007570 Celiac disease HSDN C0151889 Reflexes tendon increased C1843504 Pontocerebellar hypoplasia type 1 HPO C0020672 Body temperature decreased C0004275 Attitude health HSDN C0012833 Dizzy C0395918 Cochlear meniere syndrome UMLS C4084775 Usual severity weight loss C1145670 Respiratory failure HSDN C1963184 Nystagmus adverse event C0751267 Encephalopathy, subacute necrotizing, infantile OrphaNet|MalaCards C0015230 Exanthem C0406337 Psoriasis circinata UMLS C4085211 Pain distress question C0027927 Neurosyphilis HSDN C0030193 Sense of pain C0016719 Friedreich ataxia HSDN C1963063 Anorexia adverse event C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0007350 Cat disease HSDN C0727671 Red cross toothache drops C0027073 Myofascial pain syndromes HSDN C0424755 Fever symptoms C0037650 Somatoform disorder HSDN C0004134 Dyssynergia C1000483 Genus anemia HSDN C4085548 Usual severity dizziness C0305062 Tetanus toxoids HSDN C3887873 Hearing loss C2586211 Thrombosis of blood vessel HSDN C3146279 Coma C0011884 Diabetic retinopathy HSDN C4084773 Bothered by weight gain C0021053 Immune system diseases HSDN C0040822 D tremors C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0851578 Disorder sleep C0795623 Hepatitis a vaccine, inactivated HSDN C1557397 Adverse event associated with pain C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C0030193 Sense of pain C0020951 Immune complex diseases HSDN C0085128 Cardiac output elevated C3827868 Tachycardia by ecg finding HSDN C0857305 Thrombocytopenia purpura C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C3463815 Feel fatigue C0027658 Neoplasms, germ cell and embryonal HSDN C0026826 High muscle tone C0023521 Globoid cell leukodystrophy HSDN|HPO C3829611 Nausea frequency C0003469 Anxiety disorders HSDN C2919142 Short stature adverse event C3279792 Short-rib thoracic dysplasia 7 with or without polydactyly MalaCards C0036572 Convulsion C0086543 Cataract nos HSDN C0043094 Weight gain C0033860 Psoriasis HSDN C2984058 Have pain C0006261 Bronchial diseases HSDN C0008031 Pain chest C0023895 Liver diseases HSDN C0085636 Light sensitivity C0268495 Oculocutaneous albinism type 2 OrphaNet|HPO|MalaCards C4084774 Have weight loss C0949272 Iieocolitis MalaCards C0030554 Abnormal sensation C0009730 Spinal meningocele HSDN C0042963 Symptoms vomiting C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO|UMLS C4084773 Bothered by weight gain C1135956 Maternal fetal relations HSDN C1963087 Constipation adverse event C0003850 Arteriosclerosis HSDN C0029163 Hemorrhage mouth C0001418 Adenocarcinoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011071 Sudden death HSDN C2911647 Weight gain adverse event C0700327 Clinical findings relating to memory HSDN C0020672 Body temperature decreased C0004352 Autistic disorder HSDN C0019521 Hiccoughs C3494405 Maternal death HSDN C0424755 Fever symptoms C0033923 Psychomotor function HSDN C0234512 Prosopagnosia C0005891 Bodies image HSDN C1384666 Decreased hearing C0236736 Cocaine-related disorders HSDN C0040822 D tremors C0038395 Streptococcal infections HSDN C0020672 Body temperature decreased C0264766 Rheumatic mitral stenosis HSDN C0026821 Cramp C0041341 Tuberous sclerosis HSDN C3539890 Pelvic pain causes awakening at night C0600041 Infective cystitis HSDN C0031911 Pigment deposition C3496549 Male germ cell tumor MalaCards C0008031 Pain chest C0020741 Ibuprofen allergy UMLS C0017565 Gingiva hemorrhage C1414497 F10 gene HPO C4085211 Pain distress question C0428478 Serum triglycerides raised HSDN C0020672 Body temperature decreased C0003864 Arthritis HSDN C0426579 Anorexia symptom C0346647 Malignant neoplasm of pancreas MalaCards C4084774 Have weight loss C0006264 Bronchial neoplasms HSDN C1963252 Tremor adverse event C0041755 Adverse reaction to drug HSDN C0010200 Cough symptom C0022107 Irritable mood HSDN C0018681 Headache, cephalalgia C0009324 Ulcerative colitis HSDN C0043094 Weight gain C0030807 Pemphigus, nos HSDN C2024878 Cardiovascular surgery result: dyspnea C0007570 Celiac disease HSDN C0034150 Skin purpura C0432222 Spondyloenchondrodysplasia MalaCards C0028738 Nystagmus C0431399 Familial aplasia of the vermis MalaCards C3146279 Coma C0001364 Massive hepatic necrosis HSDN C1963180 Neck pain adverse event C0521542 Brainstem infarct HSDN C0036572 Convulsion C0265498 48, xxxy syndrome MalaCards C1963093 Dizziness adverse event C0026780 Mumps HSDN C0018681 Headache, cephalalgia C0475073 Subarachnoid hemorrhage traumatic HSDN C3463815 Feel fatigue C0035309 Retinal diseases HSDN C0242936 Center pain C0022374 Jejunal neoplasms HSDN C0000727 Abdomen acute C0008728 Churg-strauss syndrome HSDN C1384666 Decreased hearing C0013990 Pathological accumulation of air in tissues HSDN C2203646 Jaundice C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0241165 Skin thickening C0852007 Scleroderma and associated disorders OrphaNet C0011570 Monopolar depression C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C1963249 Tinnitus adverse event C0001418 Adenocarcinoma HSDN C3898969 Have been vomiting C0003850 Arteriosclerosis HSDN C0030554 Abnormal sensation C0342700 Cobalamin pseudodeficiency due to transcobalamin deficiency MalaCards C4085210 Usual severity pain C0242788 Breast neoplasms, male HSDN C0349588 Stature short C2675229 Ciliary dyskinesia, primary, 11 MalaCards|HPO C1963184 Nystagmus adverse event C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C1961131 Cough adverse event C0024198 Lyme disease HSDN C3641756 Have diarrhea C0038356 Stomach neoplasms HSDN C0037199 Sinus infection C0919524 Atm gene HPO C1279888 Proteinuria of undiagnosed cause C2931426 Orofaciodigital syndrome type1 HPO C0030486 Extremity paralysis, lower C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0012833 Dizzy C0037933 Spinal diseases HSDN C0004134 Dyssynergia C0037369 Smoking HSDN C1963252 Tremor adverse event C3489725 Pseudo-torch syndrome MalaCards C4084784 Diarrhea C0021308 Infarction HSDN C2984058 Have pain C0001828 Agricultural workers' diseases HSDN C0030193 Sense of pain C0027794 Neural tube defects HSDN C0035229 Respiratory function impaired C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards C3539890 Pelvic pain causes awakening at night C0206687 Carcinoma, endometrioid HSDN C2875625 Eyelid retraction right lower eyelid C0015397 Disorder of eye UMLS C0751837 Gait ataxic C2931325 Chromosome 22 ring MalaCards C3539022 Pelvic pain decreasing in severity C0002989 Epithelioid hemangioma of skin HSDN C0034124 Pupillary disorder C0206247 Amyloid neuropathies HSDN C1557397 Adverse event associated with pain C0023798 Lipoma HSDN C1557397 Adverse event associated with pain C0035321 Retinal tear HSDN C0014089 Functional encopresis C0021783 Internal external locus of control HSDN C0042571 Vertigo subjective C0024141 Lupus erythematosus, systemic HSDN C0011206 Delirium acute C0030297 Pancreatic neoplasm HSDN C0013404 Respiratory difficulty C0029412 Hypertrophic pulmonary osteoarthropathy HSDN C3714552 Strength decreased C0349653 Congenital disorder of glycosylation type 1a MalaCards|UMLS C0151786 Weakness muscle C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C0085636 Light sensitivity C0870082 Hyperkeratosis HSDN C1963184 Nystagmus adverse event C2931872 Free sialic acid storage disease OrphaNet|MalaCards C4084784 Diarrhea C1546635 Specimen source codes - fistula HSDN C1557397 Adverse event associated with pain C0002949 Aneurysm, dissecting HSDN C2142181 Left knee pain C0810350 Non-traumatic joint disorders UMLS C0036659 Sensation disorder C0037952 Spinocerebellar degeneration HSDN C0424755 Fever symptoms C0282607 Vascular neoplasms HSDN C1557397 Adverse event associated with pain C0018553 Hamartoma syndrome, multiple HSDN C0042963 Symptoms vomiting C0033871 Psychiatric status rating scales HSDN C1963281 Vomiting adverse event C2713347 7-dehydrocholesterol reductase deficiency MalaCards C4085317 Diarrhea frequency C0025521 Inborn errors of metabolism HSDN C0043094 Weight gain C3489413 Lipomatosis, multiple HSDN C1963066 Joint pain adverse event C1854896 Mucolipidosis iii gamma MalaCards C0040822 D tremors C0393613 Isolated facial tremor UMLS C0151889 Reflexes tendon increased C3810080 Mental retardation, autosomal recessive 40 MalaCards C1963252 Tremor adverse event C1850100 Parkinson disease 15, autosomal recessive (disorder) HPO C4084776 Weight loss C0027092 Myopia HSDN C0004604 Pain back C0014358 Enterocolitis, pseudomembranous HSDN C1557397 Adverse event associated with pain C0032371 Poliomyelitis HSDN C1963252 Tremor adverse event C0024586 Malignant carcinoid syndrome HSDN C3665347 Vision impaired C0007965 Chediak-higashi syndrome MalaCards|HPO C0018777 Deafness, conductive C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0023380 Lethargy C0041318 Tuberculosis, meningeal HSDN C0015672 Decreased energy C0483368 Human anaplasmosis due to anaplasma phagocytophilum MalaCards C2237041 Shox gene with short stature C2745953 Spondylometaphyseal dysplasia with dentinogenesis imperfecta OrphaNet C0151786 Weakness muscle C1970173 Acyl-coa dehydrogenase family, member 9, deficiency of MalaCards|HPO|UMLS C0242936 Center pain C0022078 Iris diseases HSDN C2984058 Have pain C0042485 Venous insufficiency HSDN C2024878 Cardiovascular surgery result: dyspnea C1290398 Cerebral arterial aneurysm HSDN C0036572 Convulsion C0273058 Traumatic intracranial hemorrhage HSDN C3898969 Have been vomiting C0020517 Hypersensitivity HSDN C2911647 Weight gain adverse event C1145670 Respiratory failure HSDN C4084767 Bothered by vomiting C2711591 Infection by anisakidae HSDN C0013404 Respiratory difficulty C0149725 Lower respiratory tract infection MalaCards C4084724 Usual severity constipation C0018794 Heart block HSDN C4085548 Usual severity dizziness C0018802 Congestive heart failure HSDN C0015970 Fever unknown origin C0019829 Hodgkin disease HSDN C0018991 Paralysis one side of body C0025517 Metabolic diseases HSDN C4084776 Weight loss C0015579 Family characteristics HSDN C0017672 Pain tongue C0010266 Cranial nerve diseases HSDN C0349588 Stature short C1857844 Williams-beuren region duplication syndrome MalaCards C0518090 Frequency of pain question C0024232 Lymphatic metastasis HSDN C3641755 Have constipation C0035242 Respiratory tract diseases HSDN C0015469 Facial paralysis C1546533 Specimen source codes - abscess HSDN C0018681 Headache, cephalalgia C0342257 Complications of diabetes mellitus HSDN C0013595 Eczematous dermatitis C0152094 Cellular immunodeficiency with abnormal immunoglobulin deficiency MalaCards C0151786 Weakness muscle C1261473 Sarcoma HSDN C0263540 Nail loss C0079683 Herlitz disease MalaCards|UMLS C0221150 Odynophagia C0268040 Ketoacidosis starvation UMLS C0013604 Edematous C0003152 Anterior tibial syndrome HSDN C1963170 Hypothermia adverse event C0000768 Congenital abnormality HSDN C0035229 Respiratory function impaired C1836448 Nemaline myopathy 1 HPO C3898969 Have been vomiting C0750394 Wbc low HSDN C3274924 Have been coughing C0026769 Multiple sclerosis HSDN C0028738 Nystagmus C2931258 Amaurosis congenita of leber, type 1 MalaCards|HPO C0030552 Paralysis partial C0002871 Anemia HSDN C0015970 Fever unknown origin C0007222 Cardiovascular diseases HSDN C3463815 Feel fatigue C1527311 Brain edema HSDN C4085222 Nausea C0027121 Myositis HSDN C0857305 Thrombocytopenia purpura C0022661 Kidney failure, chronic HSDN C2242996 Tingling C0025286 Meningioma HSDN C0085642 Asphyxia reticularis C0037268 Skin abnormalities HSDN C0038002 Spleen enlargement C0004576 Babesiosis OrphaNet|MalaCards C4084768 Usual severity vomiting C1962963 Osteoporosis adverse event HSDN C3539895 Pelvic pain occurs with bowel movement C0009240 Cognition HSDN C0010038 Corneal opacity disorder C4049701 Nephrotic syndrome - frequently relapsing MalaCards C4084788 Have dizziness C0037274 Dermatologic disorders HSDN C1510456 Wernicke aphasia C0026118 Situational therapy HSDN C0036572 Convulsion C0751156 Fraxa syndrome MalaCards|HPO C0009460 Communication impairment C0001973 Alcoholic intoxication, chronic HSDN C0015230 Exanthem C3714644 Thymus neoplasms MalaCards C0022638 Ketosis C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0151786 Weakness muscle C2004491 Cicatrix HSDN C2024893 Cardiovascular surgery result: fatigue C1854336 Paragangliomas 3 MalaCards C4085211 Pain distress question C0025472 Mesenteric vascular occlusion HSDN C4085862 Bothered by nausea C0017160 Gastroenteritis DiseaseOntology|HSDN C0575081 Abnormal gait C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria OrphaNet|MalaCards C0027497 Queasy C0018794 Heart block HSDN C3274924 Have been coughing C2936739 Hyper-immunoglobulin e syndrome, autosomal dominant OrphaNet|HPO C4084773 Bothered by weight gain C0559260 Congenital scoliosis HSDN C0917816 Deficiency mental C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0518090 Frequency of pain question C1704421 Skin pigmentation disorder HSDN C1557397 Adverse event associated with pain C0206696 Carcinoma, signet ring cell HSDN C0018991 Paralysis one side of body C2240378 Cleft palate on exam HSDN C4084727 Cough frequency C0343528 Legionella pneumophila; infection, nonpneumonic OrphaNet|MalaCards C0036572 Convulsion C3279627 Epilepsy, progressive myoclonic, 6 UMLS C0007758 Cerebellar ataxia C1970431 Pitt-hopkins syndrome MalaCards C4084776 Weight loss C0005396 Bile duct neoplasms HSDN C0518090 Frequency of pain question C0019624 Histiocytosis, non-langerhans-cell HSDN C0151827 Pain eye C0162566 Porphyria cutanea tarda HSDN C0000737 Abdomen pain C3714644 Thymus neoplasms HSDN C4084784 Diarrhea C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0036572 Convulsion C0242231 Coronary stenosis HSDN C2911647 Weight gain adverse event C0019196 Hepatitis c HSDN C0038990 Sweats C2930793 Achondroplastic dwarfism MalaCards C2203646 Jaundice C1881674 Medical device emits smoke HSDN C1963087 Constipation adverse event C0018674 Head trauma HSDN C4085210 Usual severity pain C1963084 Colitis adverse event HSDN C0038002 Spleen enlargement C0432219 Opsismodysplasia MalaCards|HPO C0009806 Constipate C0036677 Sensory threshold HSDN C0497406 Over weight C0013295 Duodenal ulcer HSDN C2024878 Cardiovascular surgery result: dyspnea C0021799 Interprofessional relations HSDN C4084768 Usual severity vomiting C0040425 Tonsillitis HSDN C0473235 Hematuria painless C0042075 Urologic diseases UMLS C3887873 Hearing loss C2020541 Strabismus HSDN C0005745 Blepharoptosis C1834558 Myopathy, centronuclear, autosomal dominant HPO C0518090 Frequency of pain question C0162872 Aortic aneurysm, thoracic HSDN C2315100 Pediatric failure to thrive C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0036396 Sciatica C0040136 Thyroid neoplasm HSDN C0037771 Paraparesis spastic C0162872 Aortic aneurysm, thoracic HSDN C0700078 Deep tendon reflex decrease C1706192 Sulfatidosis MalaCards C0242936 Center pain C0001420 Papillary adenocarcinoma HSDN C0242936 Center pain C3160917 Bladder pain syndrome OrphaNet|MalaCards C2032396 Pelvic pain on the right C0041954 Ureteral diseases and syndromes HSDN C0035078 Failure kidney C0085413 Polycystic kidney, autosomal dominant HPO C3203358 Alveolar hypoventilation C1366535 Avp gene HSDN C0003862 Pain joint C0032463 Polycythemia vera OrphaNet|HPO C0022660 Acute kidney failure C0342701 Transcobalamin ii deficiency OrphaNet|HPO|MalaCards C0036572 Convulsion C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C2919142 Short stature adverse event C3281235 Baraitser-winter syndrome 2 MalaCards C0018772 Deafness C0004352 Autistic disorder HSDN C2984058 Have pain C1879737 Aromatherapy and essential oils HSDN C0018681 Headache, cephalalgia C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C0010200 Cough symptom C0022665 Kidney neoplasm HSDN C4085222 Nausea C0700095 Central neuroblastoma HSDN C2237041 Shox gene with short stature C0175693 Russell-silver syndrome OrphaNet|MalaCards C0002622 Amnesias C0205788 Histiocytoid hemangioma HSDN C0476250 Head neck mass C1282205 Eyelid hemangiomas UMLS C0026838 Spasticity muscle C0575059 Spastic tetraparesis UMLS C0030193 Sense of pain C0029132 Disorder of the optic nerve HSDN C0007758 Cerebellar ataxia C0023467 Leukemia, myelocytic, acute HSDN C0857305 Thrombocytopenia purpura C0026780 Mumps HSDN C2126172 Sore on floor of mouth C0149745 Oral ulcer UMLS C0025323 Bleeding menstrual heavy C0272327 Hereditary factor x deficiency disease MalaCards C4084784 Diarrhea C0040947 Trichostrongyloidiasis HSDN C1963071 Back pain adverse event C0019270 Hernia HSDN C0917816 Deficiency mental C1858479 Spastic paraplegia 11, autosomal recessive OrphaNet|HPO|MalaCards C0427055 Face weakness C1839028 Mitochondrial myopathy with diabetes MalaCards|UMLS C1860844 Sparse, thin hair C0265336 Senter syndrome OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0036346 Schizophrenia, childhood HSDN C4084727 Cough frequency C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084788 Have dizziness C0062527 Hepatitis b vaccine HSDN C0155552 Hearing loss mixed C0022739 Klippel-trenaunay-weber syndrome HSDN C0030193 Sense of pain C0019101 Hemorrhagic fever with renal syndrome HSDN C4084897 Sleep disturbance subordinate domain C0270972 Cornelia de lange syndrome OrphaNet|HPO|MalaCards C4084727 Cough frequency C0030297 Pancreatic neoplasm HSDN C0018772 Deafness C1510428 Cerebral abscess HSDN C0038868 Supranuclear palsy progressive C0020538 Hypertensive disease HSDN C0030193 Sense of pain C0037275 Skin diseases, vesiculobullous HSDN C4042891 Sleep wake disorders C0015423 Eyelid diseases HSDN C3641756 Have diarrhea C2931542 Shapiro syndrome MalaCards C4084775 Usual severity weight loss C0017155 Gastritis, hypertrophic HSDN C0221232 Welts C0344183 Exercise anaphylaxis UMLS C4085211 Pain distress question C0358297 Anthrax vaccines HSDN C0007758 Cerebellar ataxia C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0003962 Ascites C0546323 Inferior vena cava membranous obstruction MalaCards C2187990 Unable to perform sex C1858664 Hemochromatosis, type 3 MalaCards C0015230 Exanthem C0011168 Deglutition disorders UMLS C4085211 Pain distress question C0162316 Iron deficiency anemia HSDN C0577659 Axillary pain C0741025 Chest problem UMLS C0018772 Deafness C0019284 Diaphragmatic hernia HSDN C4084768 Usual severity vomiting C0398691 Hyperimmunoglobulinemia d MalaCards|HPO C2984057 Have nausea C0020435 Hyperbilirubinemia, hereditary HSDN C4085862 Bothered by nausea C0015457 Expression facial HSDN C0015230 Exanthem C0406330 Psoriasis plantaris UMLS C0004604 Pain back C1546602 Specimen source codes - diverticulum HSDN C3665347 Vision impaired C0085209 Bovine spongiform encephalitis MalaCards C0030554 Abnormal sensation C0206734 Hemangioblastoma HSDN C4085211 Pain distress question C0003872 Arthritis, psoriatic HSDN C0019079 Bloody sputum C0014013 Empyema, pleural HSDN C3539890 Pelvic pain causes awakening at night C0001580 Adolescent behavior HSDN C4049644 Depression C0004576 Babesiosis MalaCards C4042891 Sleep wake disorders C0549567 Pigmentation disorders HSDN C4084773 Bothered by weight gain C0282616 Aids enteropathy HSDN C1000483 Genus anemia C0221026 X-linked agammaglobulinemia HPO C0557874 Global developmental delay C4014371 Immunodeficiency 23 MalaCards C4084726 Distress cough C0016548 Foreign body migration HSDN C0424755 Fever symptoms C0597109 Nurse's role HSDN C2237041 Shox gene with short stature C2932714 Pontocerebellar hypoplasia type 2 MalaCards C0042940 Disorder of voice C0393593 Dystonia disorders HSDN C0026821 Cramp C0023264 Leigh disease HSDN C4084774 Have weight loss C1704275 Pyomyositis OrphaNet|MalaCards C3641756 Have diarrhea C0043168 Whooping cough due to unspecified organism HSDN C4084727 Cough frequency C0012691 Dislocations HSDN C0427068 Legs weakness C0027577 Nelson syndrome OrphaNet|MalaCards C4084773 Bothered by weight gain C2186740 Reported urticaria HSDN C0242936 Center pain C0001623 Adrenal gland hypofunction HSDN C0011991 Loose stools C0023903 Liver neoplasms MalaCards C0000737 Abdomen pain C0854932 Stage ii ovarian dysgerminoma UMLS C0231712 Gait waddling C2745959 Spondyloepiphyseal dysplasia, congenita MalaCards|HPO|UMLS C0004134 Dyssynergia C0021295 Infant, premature, diseases HSDN C1963093 Dizziness adverse event C0520679 Sleep apnea, obstructive HSDN C0011991 Loose stools C0041408 Turner syndrome HSDN C2237041 Shox gene with short stature C1860788 Transient myeloproliferative disorder of down syndrome HPO C0009676 Confusion state C0032087 Plant poisoning HSDN C0518090 Frequency of pain question C0000821 Threatened abortion HSDN C2024878 Cardiovascular surgery result: dyspnea C1112486 Aggressive systemic mastocytosis MalaCards C4084784 Diarrhea C0021070 Immunoproliferative disease HSDN C0221263 Cafe au lait spot C0004941 Behavioral symptoms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014059 Encephalomyelitis, acute disseminated HSDN C0036572 Convulsion C1527298 Dysentery, bacillary HSDN C4084768 Usual severity vomiting C0010054 Coronary arteriosclerosis HSDN C0426579 Anorexia symptom C0314657 Genetic predisposition HSDN C2911645 Weight loss adverse event C0015625 Fanconi anemia MalaCards|HPO C0424755 Fever symptoms C0020452 Hyperemia HSDN C0427055 Face weakness C3501858 Muscular dystrophy, limb-girdle, type 1d MalaCards C0036572 Convulsion C0004239 Atrial flutter HSDN C0041834 Erythematous condition C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C4084774 Have weight loss C0011633 Dermatomyositis OrphaNet|HSDN|MalaCards C0034155 Thrombotic thrombocytopenic purpura C0026654 Moyamoya disease HSDN C0000727 Abdomen acute C0026269 Mitral valve stenosis HSDN C0018681 Headache, cephalalgia C0085298 Sudden cardiac death HSDN C0042514 Ventricular tachycardia C3151204 Cardiomyopathy, familial hypertrophic, 16 HPO C0010200 Cough symptom C1455705 Pulmonary histiocytosis x OrphaNet|MalaCards C0162298 Stiffness joints C2931323 Heart-hand syndrome 2 OrphaNet|MalaCards C0007758 Cerebellar ataxia C0268281 Infantile neuronal ceroid lipofuscinosis OrphaNet|HPO|MalaCards C0086565 Liver function abnormal C0346647 Malignant neoplasm of pancreas MalaCards C0030193 Sense of pain C0085215 Ovarian failure, premature HSDN C0020538 Hbp C1510460 Orofaciodigital syndrome i MalaCards|HPO C0030193 Sense of pain C0392784 Dermatofibrosarcoma protuberans HSDN C0521628 Genital itching male C0017412 Genital diseases, male UMLS C4084776 Weight loss C0007784 Cerebral hemisphere hemorrhage HSDN C0038002 Spleen enlargement C1858558 Rheumatoid arthritis, systemic juvenile MalaCards C0349506 Sun sensitivity C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C2984058 Have pain C3668816 Inflammation of non-human mammary gland HSDN C0030794 Pelvis pain C0037286 Skin neoplasms HSDN C0812426 Kidney problem C0035085 Kidney, infarction UMLS C0162834 Hyperpigmentation C2931366 Congenital deformity of the thumb and congenital alopecia MalaCards C2911647 Weight gain adverse event C0020522 Delayed hypersensitivity HSDN C0016204 Fart C0079487 Helicobacter infections HSDN C0027066 Myoclonic jerking C2746067 Spinocerebellar ataxia 22 HPO C0033774 Skin pruritus C1852296 Darier disease, acral hemorrhagic type HPO C0007758 Cerebellar ataxia C0041466 Typhoid fever OrphaNet|MalaCards C1384666 Decreased hearing C1856476 Gaucher disease, type iiic OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0040411 Tongue neoplasms HSDN C0036572 Convulsion C0268680 Biotin deficiency MalaCards C0039070 Collapse fleeting C0022744 Knee injury HSDN C0004604 Pain back C0043254 Injuries penetrating HSDN C4085549 Dizziness C0040997 Trigeminal neuralgia HSDN C0011206 Delirium acute C0752332 Lupus vasculitis, central nervous system HSDN C0011991 Loose stools C0035457 Rhinitis, allergic, perennial HSDN C0518090 Frequency of pain question C0041408 Turner syndrome HSDN C0042963 Symptoms vomiting C0014858 Esophageal motility disorders UMLS C0018524 Hallucinate C0025286 Meningioma HSDN C0011991 Loose stools C0342701 Transcobalamin ii deficiency MalaCards|UMLS C4084897 Sleep disturbance subordinate domain C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C0019209 Large liver C1865614 Hemochromatosis, type 2a MalaCards|HPO C0027796 Neuralgias C0038358 Gastric ulcer HSDN C0011168 Disorder deglutition C3501858 Muscular dystrophy, limb-girdle, type 1d MalaCards C0277986 Edema gum C0542571 Facial edema UMLS C0241210 Speaking delay C3810406 Mental retardation, autosomal dominant 23 MalaCards C0020505 Excessive eating C1704373 Compulsive personality disorder HSDN C0007642 Cellulitis nos C0264005 Fasciitis, eosinophilic OrphaNet|MalaCards C4050613 Anxiety C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0018524 Hallucinate C0011884 Diabetic retinopathy HSDN C4084769 Vomiting frequency C0003047 Animal disease HSDN C0029163 Hemorrhage mouth C2984289 Melanoma pathway HSDN C1963087 Constipation adverse event C0040053 Thrombosis HSDN C0004134 Dyssynergia C2930997 Congenital disorder of glycosylation type 1c MalaCards|UMLS C1963077 Bone pain adverse event C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C4085317 Diarrhea frequency C0042870 Vitamin d deficiency HSDN C4084802 Usual severity diarrhea C1832370 Myopathy, myofibrillar, desmin-related MalaCards|HPO C2984058 Have pain C0035066 Renal artery obstruction HSDN C0008031 Pain chest C1881712 Medical device material rupture HSDN C2242996 Tingling C0158454 Malunited fracture HSDN C4084775 Usual severity weight loss C2240378 Cleft palate on exam HSDN C0015970 Fever unknown origin C3495422 Finding relating to sexuality and sexual activity HSDN C1557397 Adverse event associated with pain C1414542 Fbn1 gene HSDN C0151311 Cranial nerve palsy C0544862 Neurocutaneous melanosis HPO C4042891 Sleep wake disorders C0032969 Pregnancy in diabetics HSDN C1963091 Diarrhea adverse event C3149378 Immunodeficiency, common variable, 1 MalaCards|HPO C2242996 Tingling C0036202 Sarcoidosis HSDN C4085210 Usual severity pain C0162830 Dermatitis, phototoxic HSDN C3665346 Loss sight C0342287 Thiamine responsive megaloblastic anemia syndrome MalaCards|HPO C1963274 Vasculitis adverse event C0340992 Cryoglobulinemic; vasculitis OrphaNet|MalaCards C0026838 Spasticity muscle C1969645 Ataxia, spastic, 3, autosomal recessive MalaCards|HPO|UMLS C0013456 Pain ear C0018671 Head and neck neoplasms HSDN C0034155 Thrombotic thrombocytopenic purpura C0007820 Cerebrovascular disorders HSDN C0522224 Palsied C0409354 Flexion contracture of hip HSDN C0042963 Symptoms vomiting C1009209 Tinea HSDN C0020305 Fetal edema C0265274 Achondrogenesis, type ib (disorder) OrphaNet|HPO C1069915 Vertigo C1457883 Aggressive reaction HSDN C4084774 Have weight loss C0008149 Chlamydia infections HSDN C0557874 Global developmental delay C3179455 Niemann-pick disease, type c1 MalaCards|HPO C0262384 Chest pain atypical C0018799 Heart diseases UMLS C2029884 Hearing loss by exam C0001969 Alcoholic intoxication HSDN C0008031 Pain chest C2004491 Cicatrix HSDN C4085317 Diarrhea frequency C0029295 Oropharyngeal neoplasms HSDN C0018772 Deafness C2936862 Bardet-biedl syndrome 1 (disorder) MalaCards C0151686 Growth retardation C1851443 Cerebrooculofacioskeletal syndrome 3 HPO C0033774 Skin pruritus C0034929 Reflex HSDN C0023012 Delay language C3495551 Dihydropyrimidinuria MalaCards C0027796 Neuralgias C0154723 Migraine with aura HSDN C4085548 Usual severity dizziness C0038160 Staphylococcal infections HSDN C1313921 Urinomas C0005695 Bladder neoplasm HSDN C1963137 Hydrocephalus adverse event C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy HPO C0398650 Idiopathic thrombocytopenia purpura C0025202 Melanoma HSDN C0332573 Macula C0432362 Tuberous sclerosis, ash leaf spot UMLS C0010520 Skin cyanosis C0002878 Anemia, hemolytic HSDN C3641755 Have constipation C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO C0232466 Feeding difficulty C1850674 Minicore myopathy with external ophthalmoplegia (disorder) MalaCards C4085317 Diarrhea frequency C0026865 Mushroom poisoning HSDN C0239385 Extremity paresthesia C0030554 Paresthesia UMLS C0917816 Deficiency mental C1845892 Hprt deficiency, neurologic variant HPO C2237041 Shox gene with short stature C2675861 Lipodystrophy, congenital generalized, type 3 MalaCards|HPO C0242936 Center pain C0008370 Cholestasis HSDN C3641756 Have diarrhea C0042487 Venous thrombosis HSDN C1549543 Administration method - pain C0008325 Cholecystitis HSDN C4085211 Pain distress question C0041408 Turner syndrome HSDN C3827868 Tachycardia by ecg finding C1857338 Deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy MalaCards C0015469 Facial paralysis C1858717 Facial paresis, hereditary, congenital MalaCards C0015672 Decreased energy C0027726 Nephrotic syndrome HSDN C1510417 Apraxia of gait C0236642 Pick disease of the brain HSDN C1963065 Apnea adverse event C1414203 Dws gene HSDN C0036572 Convulsion C0015423 Eyelid diseases HSDN C3641756 Have diarrhea C0030299 Pancreatic pseudocyst HSDN C4084723 Constipation C0162565 Acute intermittent porphyria OrphaNet|HSDN|HPO|MalaCards C0020673 Hypothermia (central) (local) C0036984 Shock, surgical HSDN C1963087 Constipation adverse event C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards C1384666 Decreased hearing C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C2911645 Weight loss adverse event C0003869 Arthritis, infectious HSDN C0518090 Frequency of pain question C0039373 Tay-sachs disease HSDN C0020672 Body temperature decreased C1962971 Myocarditis adverse event HSDN C0030200 Intractable pain C0560651 Spinal cord syndrome central HSDN C0497406 Over weight C0019829 Hodgkin disease HSDN C4085211 Pain distress question C0027121 Myositis HSDN C0151889 Reflexes tendon increased C0796126 Aicardi-goutieres syndrome 1 MalaCards C0003079 Pupillary inequality C1290398 Cerebral arterial aneurysm HSDN C0878773 Bladder hyperactive C0003811 Cardiac arrhythmia HSDN C0030193 Sense of pain C0033075 Presbyopia HSDN C0004134 Dyssynergia C0014836 Escherichia coli infections HSDN C0023380 Lethargy C0342720 Adenosylcobalamin synthesis defect MalaCards C0019214 Hepatosplenomegaly C1856303 Gsd iv, neuromuscular form, fatal perinatal HPO C4085549 Dizziness C0006309 Brucellosis HSDN C0085636 Light sensitivity C0085409 Polyendocrinopathies, autoimmune HSDN C1263846 Attention deficit disorder with hyperactivity C0175691 Dubowitz syndrome OrphaNet|HPO|MalaCards C1145670 Failure respiratory C0019101 Hemorrhagic fever with renal syndrome OrphaNet|MalaCards C0242936 Center pain C0002940 Aneurysm HSDN C2048468 Inability to impregnate C0403812 Male infertility with large-headed, multiflagellar, polyploid spermatozoa MalaCards|HPO C0030552 Paralysis partial C0042133 Uterine fibroids HSDN C0042963 Symptoms vomiting C0342873 Glutaric aciduria iii MalaCards|HPO|UMLS C0424755 Fever symptoms C0038379 Eye deviation HSDN C0042024 Urine incontinence C0022758 Kap HSDN C0011991 Loose stools C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C0850758 Pain pelvic C0432264 Axial osteosclerosis MalaCards C2984058 Have pain C0027540 Necrosis HSDN C3641755 Have constipation C0025289 Meningitis HSDN C0018681 Headache, cephalalgia C0013124 Behavior drinking HSDN C0398650 Idiopathic thrombocytopenia purpura C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084788 Have dizziness C0018081 Gonorrhea HSDN C0035229 Respiratory function impaired C0036391 Schwartz-jampel syndrome MalaCards|HPO C0241700 Voice fatigue C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C4084769 Vomiting frequency C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO C0036572 Convulsion C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C1856661 Cornea cloudy C0406556 Hereditary acrokeratotic poikiloderma of weary MalaCards|HPO C0009398 Color vision defects C2750720 Cone-rod dystrophy 13 MalaCards|HPO C2984058 Have pain C0022593 Keratosis HSDN C0424755 Fever symptoms C0035066 Renal artery obstruction HSDN C1384666 Decreased hearing C0086652 Mucopolysaccharidosis type ivb MalaCards|HPO C0019572 Hairiness C1859568 Bardet-biedl syndrome 10 HPO C2911645 Weight loss adverse event C0017636 Glioblastoma HSDN C0039070 Collapse fleeting C0003864 Arthritis HSDN C0030554 Abnormal sensation C0002986 Fabry disease MalaCards|HPO C4085211 Pain distress question C0023267 Fibroid tumor HSDN C4084775 Usual severity weight loss C1546635 Specimen source codes - fistula HSDN C2362324 Pediatric obesity C0036239 Satiety HSDN C0750426 Wbc elevated C3279664 Emberger syndrome MalaCards C4085862 Bothered by nausea C0521607 Peritoneal fibrosis HSDN C1963086 Confusion adverse event C0221021 Microangiopathic hemolytic anemia MalaCards C0030552 Paralysis partial C0206641 Osteochondromatosis OrphaNet|HPO C0024031 Back pain lower back C2931642 Benign symmetrical lipomatosis HSDN C0033377 Caudal displacement C1855675 Arima syndrome OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0026771 Trauma multiple HSDN C0242936 Center pain C0001486 Adenovirus infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0009952 Febrile convulsions HSDN C0151786 Weakness muscle C4039473 3-methylglutaconic aciduria type 5 MalaCards C0009421 Comatose C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C4085211 Pain distress question C0521585 Gastrointestinal mucositis HSDN C0008031 Pain chest C0007133 Carcinoma, papillary HSDN C1963281 Vomiting adverse event C0235833 Congenital diaphragmatic hernia HSDN C0000737 Abdomen pain C1333979 Hepatitis virus-related hepatocellular carcinoma UMLS C0037771 Paraparesis spastic C4225250 Spastic paraplegia 75, autosomal recessive UMLS C0026821 Cramp C0206708 Cervical intraepithelial neoplasia HSDN C4085211 Pain distress question C0007868 Cervical dysplasia HSDN C0042025 Urinary incontinence stress C0041956 Ureteral obstruction HSDN C0085636 Light sensitivity C0035333 Retinitis HSDN C0013404 Respiratory difficulty C0036323 Schistosomiasis HSDN C4084776 Weight loss C0856761 Budd-chiari syndrome MalaCards|HPO C4084776 Weight loss C0268151 Classical galactosemia OrphaNet|HPO|MalaCards C0848203 Male pelvic pain C0019294 Hernia, inguinal HSDN C2911645 Weight loss adverse event C0085632 Apathy HSDN C3641756 Have diarrhea C0012546 Diphtheria HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0242707 Ventricular dysfunction, right HSDN C0030193 Sense of pain C0017152 Gastritis HSDN C0030193 Sense of pain C0024131 Lupus vulgaris HSDN C2919142 Short stature adverse event C0342488 Mineralocorticoid excess syndrome, apparent MalaCards C0010200 Cough symptom C0152264 Familial erythrocytosis HPO C0036572 Convulsion C0796135 Renpenning syndrome 1 HPO C0013421 Dystonia C0043251 Wounds and injuries HSDN C4084766 Vomiting C0014854 Esophageal diverticulum HSDN C4085552 Dry mouth C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0030193 Sense of pain C0025297 Viral meningitis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0030286 Pancreatic diseases HSDN C0030552 Paralysis partial C0037933 Spinal diseases HSDN C0332606 Facies elfin C1867023 Cleft palate large ears small head OrphaNet|MalaCards C0152020 Atony stomach C1864668 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4 MalaCards C2203646 Jaundice C0037274 Dermatologic disorders HSDN C0041657 Consciousness loss C0014556 Epilepsy, temporal lobe HSDN C0497406 Over weight C0036439 Scoliosis, unspecified HSDN C1963252 Tremor adverse event C0017636 Glioblastoma HSDN C0012833 Dizzy C0042487 Venous thrombosis HSDN C4085211 Pain distress question C0032002 Pituitary diseases HSDN C2237041 Shox gene with short stature C1857553 Hsd11b2, arg208cys HPO C4084784 Diarrhea C1963064 Anxiety adverse event HSDN C3274924 Have been coughing C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C2132198 Abnormal blistering of the skin C1148551 X-linked dyskeratosis congenita MalaCards C4084769 Vomiting frequency C0015408 Eye injury HSDN C4084788 Have dizziness C0151699 Intracranial hemorrhages HSDN C4084784 Diarrhea C0242550 Behavior, risk reduction HSDN C4085210 Usual severity pain C1254288 Anthrax HSDN C1963249 Tinnitus adverse event C2586211 Thrombosis of blood vessel HSDN C0040264 Ear ringing sound C0453996 Tobacco smoking HSDN C0000737 Abdomen pain C3463824 Myelodysplastic syndrome HSDN C0027066 Myoclonic jerking C0268560 Hyperglycinemia, transient neonatal HPO C0012833 Dizzy C0027831 Neurofibromatosis 1 HSDN C2024878 Cardiovascular surgery result: dyspnea C0003469 Anxiety disorders HSDN C3146279 Coma C0021053 Immune system diseases HSDN C0027497 Queasy C1963064 Anxiety adverse event HSDN C0035229 Respiratory function impaired C1838979 Mitochondrial complex i deficiency MalaCards C4084774 Have weight loss C0206172 Diabetic foot HSDN C1963093 Dizziness adverse event C0002871 Anemia HSDN C0856127 Micturition disorder aggravated C0042035 Urination disorders UMLS C4084768 Usual severity vomiting C1963198 Pancreatitis adverse event HSDN C0042798 Vision dim C0221060 Mobius syndrome MalaCards|HPO C3665386 Abnormal vision C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards C0851578 Disorder sleep C0270327 Bedwetting HSDN C2242996 Tingling C2931902 Acute brachial neuritis MalaCards C0002962 Angina C0406817 Collagenoma, familial cutaneous MalaCards C0015970 Fever unknown origin C0025469 Mesenteric adenitis HSDN C4084775 Usual severity weight loss C0241158 Cicatrix skin HSDN C4085210 Usual severity pain C0010276 Craniopharyngioma HSDN C0019825 Voice hoarseness C1866552 Paragangliomas 2 (disorder) MalaCards C0042571 Vertigo subjective C0038356 Stomach neoplasms HSDN C0033774 Skin pruritus C0570374 Niacin adverse reaction UMLS C0013604 Edematous C0596263 Carcinogenesis HSDN C0240715 Perineal lump C0574913 Perineal warts UMLS C0015672 Decreased energy C1263846 Attention deficit hyperactivity disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C4084971 Trachoma HSDN C3641756 Have diarrhea C0241802 Arthritis, venereal MalaCards C4084726 Distress cough C0854421 Hanta viral infections MalaCards C0041657 Consciousness loss C0007682 Cns disorder HSDN C1963184 Nystagmus adverse event C1857588 Amaurosis hypertrichosis OrphaNet|HPO|MalaCards C4084725 Usual severity cough C0033968 Psychotherapeutic technique HSDN C1963093 Dizziness adverse event C0085183 Neoplasms, second primary HSDN C4084784 Diarrhea C0040809 Patient refusal of treatment HSDN C4084723 Constipation C0017638 Glioma HSDN C0009460 Communication impairment C0751865 Alcohol-induced disorders, nervous system HSDN C0587058 Upper extremity paresthesia C0741096 Upper_ext problem UMLS C0030552 Paralysis partial C0268228 Neuraminidase 1 deficiency HPO C4085317 Diarrhea frequency C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C3463815 Feel fatigue C0162526 Aids-related opportunistic infections HSDN C2911647 Weight gain adverse event C0021364 Male infertility HSDN C0557874 Global developmental delay C0796099 Cleft lip-palate with abnormal thumbs and microcephaly MalaCards C4085317 Diarrhea frequency C0027670 Neoplastic endocrine-like syndromes HSDN C0030552 Paralysis partial C3536983 Familial hypophosphatemic rickets HSDN C1963170 Hypothermia adverse event C0018809 Heart neoplasm HSDN C0270948 Neurogenic muscular atrophy C0795865 Chromosome 17, trisomy 17p MalaCards C3203358 Alveolar hypoventilation C0039538 Teratoma HSDN C4084784 Diarrhea C0079731 B-cell lymphomas HSDN C4084788 Have dizziness C0036690 Septicemia HSDN C0751837 Gait ataxic C0035410 Rhabdomyolysis MalaCards C1549543 Administration method - pain C0206696 Carcinoma, signet ring cell HSDN C0795692 Lactate blood increased C0518449 Control of hip fracture risk HSDN C3898969 Have been vomiting C1449842 Pseudohypoaldosteronism, type i, autosomal dominant HPO C4084723 Constipation C1833661 Paroxysmal extreme pain disorder OrphaNet|HPO|MalaCards C0024032 Birth weight subnormal C1866505 Ichthyosis, congenital, with trichothiodystrophy HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0266836 Infantile colic HSDN C0011991 Loose stools C0042870 Vitamin d deficiency HSDN C0917816 Deficiency mental C3495483 Amish brittle hair syndrome MalaCards C0025287 Meningitis-like C0041473 Camp fever HSDN C0009792 Consciousness disorder C0020258 Hydrocephalus, normal pressure HSDN C1549543 Administration method - pain C0022367 Jaw, edentulous, partially HSDN C4084773 Bothered by weight gain C0031039 Effusion pericardial HSDN C0028738 Nystagmus C1275336 Hashimoto-pritzker syndrome MalaCards|HPO C0030193 Sense of pain C4076283 Neuralgia co-occurrent with human immunodeficiency virus infection UMLS C0038002 Spleen enlargement C0036472 Scrub typhus DiseaseOntology|MalaCards C1549543 Administration method - pain C3668816 Inflammation of non-human mammary gland HSDN C0424755 Fever symptoms C0003496 Aortic rupture HSDN C0007758 Cerebellar ataxia C1258104 Diffuse scleroderma HSDN C0013404 Respiratory difficulty C0700095 Central neuroblastoma HSDN C2911647 Weight gain adverse event C0022660 Kidney failure, acute HSDN C3274924 Have been coughing C0006271 Bronchiolitis MalaCards C2237041 Shox gene with short stature C0033788 Pseudo-hurler polydystrophy OrphaNet|HPO|MalaCards C2203646 Jaundice C0033348 Language program HSDN C0004604 Pain back C1334410 Localized primitive neuroectodermal tumor MalaCards C0242936 Center pain C0242891 Injuries teeth HSDN C0018524 Hallucinate C0036421 Systemic scleroderma HSDN C4084773 Bothered by weight gain C3888013 Hypnoses HSDN C1962972 Proteinuria adverse event C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome MalaCards|HPO C3887784 Decreased urine output C0038819 Siriasis HSDN C0086439 Activity decreased C0023903 Liver neoplasms HSDN C1549543 Administration method - pain C0032310 Pneumonia, viral HSDN C1963086 Confusion adverse event C0085094 Head injury closed HSDN C0009763 Conjunctiva inflammation C0038325 Stevens-johnson syndrome HPO C3274924 Have been coughing C0003467 Anxiety HSDN C1962972 Proteinuria adverse event C0314657 Genetic predisposition HSDN C0751495 Seizure focal C0234978 Epilepsy, jacksonian UMLS C3898969 Have been vomiting C0270858 Abdominal migraines MalaCards C0036572 Convulsion C1858854 Megalencephalic leukoencephalopathy with subcortical cysts HPO|UMLS C0040264 Ear ringing sound C0460137 Push down or depress HSDN C1860844 Sparse, thin hair C0543816 Cardiocutaneous syndrome MalaCards C2984058 Have pain C0017086 Gangrene HSDN C2919142 Short stature adverse event C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0027438 Nasopharynx HSDN C0036572 Convulsion C1970095 Cleft palate, isolated, and mental retardation HPO C4085862 Bothered by nausea C0428977 Bradycardia HSDN C2911645 Weight loss adverse event C0018671 Head and neck neoplasms HSDN C4084773 Bothered by weight gain C0035309 Retinal diseases HSDN C4085210 Usual severity pain C0014378 Enterovirus infections HSDN C0030554 Abnormal sensation C2936779 Hydroxymethylbilane synthase deficiency MalaCards C1549543 Administration method - pain C1827268 Keratoacanthoma of eyelid HSDN C4084768 Usual severity vomiting C0013295 Duodenal ulcer HSDN C2024878 Cardiovascular surgery result: dyspnea C0302148 Blood clot HSDN C2315100 Pediatric failure to thrive C3150707 Chromosome 14q11-q22 deletion syndrome MalaCards C4085661 Usual severity nausea C0878544 Cardiomyopathies HSDN C1527344 Dysphonia C0040588 Tracheoesophageal fistula HSDN C1384666 Decreased hearing C0431406 Asymmetric crying face association OrphaNet C0033774 Skin pruritus C0020541 Hypertension, portal HSDN C0027796 Neuralgias C0796561 Melanoma vaccines HSDN C0086565 Liver function abnormal C3489725 Pseudo-torch syndrome MalaCards C0018834 Brash C1258104 Diffuse scleroderma HSDN C0427068 Legs weakness C1847823 Charcot-marie-tooth disease, axonal, type 2f OrphaNet|HPO|MalaCards C4085211 Pain distress question C0021846 Intestinal polyps HSDN C3898969 Have been vomiting C0003950 Ascariasis HSDN C0036572 Convulsion C0043325 Xanthomatosis HSDN C0035078 Failure kidney C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0812426 Kidney problem C2364010 Nephritis chronic UMLS C1963091 Diarrhea adverse event C0037926 Compression of spinal cord HSDN C0035229 Respiratory function impaired C3553374 Coenzyme q10 deficiency, primary, 5 MalaCards C0005779 Clotting C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C4084773 Bothered by weight gain C0162871 Aortic aneurysm, abdominal HSDN C4042891 Sleep wake disorders C0018099 Gout HSDN C1384666 Decreased hearing C1834712 Cerebellar granule cell hypertrophy and megalencephaly HPO C3829611 Nausea frequency C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C1963087 Constipation adverse event C0042138 Uterine neoplasms HSDN C1145670 Failure respiratory C0271829 Pendred's syndrome MalaCards|HPO C1963091 Diarrhea adverse event C0003838 Arterial occlusive diseases HSDN C4085211 Pain distress question C0029118 Opportunistic infections HSDN C0010200 Cough symptom C0149931 Migraine disorders HSDN C4085222 Nausea C0009450 Disease caused by microorganism HSDN C0033774 Skin pruritus C2608083 Cholestasis, benign recurrent intrahepatic 2 MalaCards|HPO C0016382 Cutaneous vascular engorgement C3665333 Keratitis-ichthyosis-deafness syndrome OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C2677613 Chromosome 15q13.3 microdeletion syndrome HPO C4084784 Diarrhea C0029401 Osteitis deformans HSDN C0497406 Over weight C1546949 Event consequence - death HSDN C0036572 Convulsion C1847874 Phace association MalaCards|UMLS C4084767 Bothered by vomiting C0031046 Pericarditis HSDN C1963170 Hypothermia adverse event C0018824 Heart valve disease HSDN C0023014 Developmental disorder language C0005941 Bone diseases, developmental HSDN C4084776 Weight loss C0011649 Dermoid cyst HSDN C0018991 Paralysis one side of body C0007282 Carotid stenosis HSDN C4084802 Usual severity diarrhea C2749485 Nblst1 HPO C0020672 Body temperature decreased C0011606 Exfoliative dermatitis HSDN C3814874 Loss of appetite question C0007932 Chagas' disease + no organ inv DiseaseOntology C4084726 Distress cough C0220981 Metabolic acidosis HSDN C0391860 Diffuse inflammations C0021368 Inflammation UMLS C4084802 Usual severity diarrhea C3150752 Agammaglobulinemia 4, autosomal recessive HPO C0013395 Indigestion C0020456 Hyperglycemia HSDN C2242996 Tingling C1963198 Pancreatitis adverse event HSDN C4084802 Usual severity diarrhea C0040034 Thrombocytopenia HSDN C4084767 Bothered by vomiting C0268543 Hyperammonemia, type iii MalaCards|HPO C0031911 Pigment deposition C0030354 Papilloma MalaCards C1963086 Confusion adverse event C0024530 Malaria HSDN C0003550 Broca aphasia C1527311 Brain edema HSDN C0042571 Vertigo subjective C1701938 Associated pulmonary arterial hypertension OrphaNet C0007758 Cerebellar ataxia C0042138 Uterine neoplasms HSDN C0413252 Hypothermia due to exposure C0007125 Carcinoma, ehrlich tumor HSDN C4085548 Usual severity dizziness C1962976 Ventricular fibrillation adverse event HSDN C2203646 Jaundice C0002792 Anaphylaxis HSDN C0005745 Blepharoptosis C0175704 Leopard syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C1961100 Erectile dysfunction adverse event HSDN C0521592 Mouth numbing C0026636 Mouth diseases UMLS C3658248 Enlarged waist elevated triglycerides C0011849 Diabetes mellitus HSDN C4084776 Weight loss C0011334 Dental caries HSDN C0018524 Hallucinate C0032227 Pleural effusion disorder HSDN C4084726 Distress cough C0005686 Urinary bladder diseases HSDN C0009676 Confusion state C1456784 Paranoia HSDN C0424755 Fever symptoms C4050613 Anxiety scale (basc-2) HSDN C0003113 Anomia C0007772 Intracranial arteriovenous malformation HSDN C0040264 Ear ringing sound C1552262 Nurse practitioner - family HSDN C4084802 Usual severity diarrhea C0236664 Alcohol-related disorders HSDN C0022346 Yellow skin C1335302 Pancreatic ductal adenocarcinoma UMLS C0423715 Testicular neuralgia C3661942 Genitofemoral neuropathy UMLS C0012833 Dizzy C0271375 Cranial nerve palsy iv trochlear HSDN C0040259 Tinea pedis C0376547 Aromatherapy HSDN C0242936 Center pain C0036346 Schizophrenia, childhood HSDN C0011991 Loose stools C0334282 Alpha-cell tumor, malignant UMLS C0026821 Cramp C1556061 Electric injuries HSDN C1565249 Limitation, mobility C0574960 Sacroiliitis HSDN C0027796 Neuralgias C0020676 Hypothyroidism HSDN C0424755 Fever symptoms C0030807 Pemphigus, nos HSDN C4084784 Diarrhea C1855849 Bartter syndrome, antenatal , type 2 HPO C2919142 Short stature adverse event C2931803 Deletion 11p13 OrphaNet|HPO C1961131 Cough adverse event C0023788 Whipple disease MalaCards C0000737 Abdomen pain C1335305 Intraductal papillary-mucinous neoplasm of pancreas with moderate dysplasia UMLS C0518090 Frequency of pain question C0001623 Adrenal gland hypofunction HSDN C2984057 Have nausea C0026848 Myopathy HSDN C0034124 Pupillary disorder C0152177 Trigeminal neuropathy HSDN C0013404 Respiratory difficulty C0029456 Osteoporosis HSDN C0542476 Forgetful C0006035 Borrelia infections MalaCards C0039070 Collapse fleeting C2004491 Cicatrix HSDN C1384666 Decreased hearing C0524801 Retinal neoplasms HSDN C0518090 Frequency of pain question C0010414 Infection by cryptococcus neoformans HSDN C1384666 Decreased hearing C0391826 Lhermitte-duclos disease MalaCards|HPO C4084776 Weight loss C0024232 Lymphatic metastasis HSDN C0018784 Deafness sensorineural C0025958 Microcephaly HSDN C0233794 Memory impaired C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C0029163 Hemorrhage mouth C0002874 Aplastic anemia HSDN C0020578 Hyperventilate C1690964 Cataract HSDN C4085222 Nausea C0043528 Zoonoses HSDN C0042571 Vertigo subjective C4049644 Depression HSDN C0023012 Delay language C0003537 Aphasia MalaCards C0162429 Dietary deficiency C2675184 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis MalaCards|HPO C0018991 Paralysis one side of body C0029124 Optic atrophy HSDN C4084724 Usual severity constipation C0012817 Diverticulum HSDN C0575081 Abnormal gait C1876175 Ataxia-telangiectasia variant MalaCards C0030794 Pelvis pain C0007867 Cervix diseases HSDN C1557397 Adverse event associated with pain C1861172 Venous thromboembolism HSDN C4085548 Usual severity dizziness C0015408 Eye injury HSDN C0013362 Dysarthrias C2931246 Chromosome 17, trisomy 17p11 2 OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0023891 Liver cirrhosis, alcoholic HSDN C4084776 Weight loss C0596263 Carcinogenesis HSDN C2984058 Have pain C0085215 Ovarian failure, premature HSDN C0011991 Loose stools C0011311 Dengue fever MalaCards|HSDN C2911645 Weight loss adverse event C0016977 Gall bladder diseases HSDN C0009806 Constipate C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0034155 Thrombotic thrombocytopenic purpura C0752299 Sleep wake transition disorders HSDN C2024878 Cardiovascular surgery result: dyspnea C0796070 Microphthalmia, syndromic 7 MalaCards C0010200 Cough symptom C0040053 Thrombosis HSDN C1313921 Urinomas C0003962 Ascites HSDN C0015672 Decreased energy C0268450 Gitelman syndrome HSDN C0009421 Comatose C0024198 Lyme disease HSDN C0036572 Convulsion C1762616 Meningioma, benign, no icd-o subtype MalaCards C0917816 Deficiency mental C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C0030554 Abnormal sensation C0007097 Carcinomas HSDN C0000727 Abdomen acute C0600260 Lung diseases, obstructive HSDN C0020305 Fetal edema C0334123 Histiocytosis, lipoid MalaCards C2237041 Shox gene with short stature C0041409 Turner syndrome, male MalaCards|HPO C4084775 Usual severity weight loss C0004352 Autistic disorder HSDN C0043094 Weight gain C0342543 Precocious puberty, central OrphaNet|MalaCards C0011991 Loose stools C0040128 Thyroid diseases HSDN C4085211 Pain distress question C0311277 Obesity, abdominal HSDN C0015970 Fever unknown origin C0085399 Ehrlichiosis HSDN C0031256 Petechia C0393591 Aicardi-goutieres syndrome HPO C2024878 Cardiovascular surgery result: dyspnea C0030920 Peptic ulcer HSDN C0036572 Convulsion C0079588 Ichthyosis, x-linked MalaCards C0085688 Engorgement breast C0405323 Breast engorgement in pregnancy, the puerperium or lactation - delivered with postnatal complication UMLS C2029884 Hearing loss by exam C0011989 Camurati-engelmann syndrome HSDN C4084769 Vomiting frequency C0038941 Incisional infection HSDN C4084773 Bothered by weight gain C0795623 Hepatitis a vaccine, inactivated HSDN C0013604 Edematous C0019189 Hepatitis, chronic HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0016196 Chest flail HSDN C3815497 Cough C0206628 Mesoblastic nephroma HSDN C3815497 Cough C0020732 Iatrogenic disease HSDN C0005745 Blepharoptosis C0162671 Melas syndrome OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0007193 Cardiomyopathy, dilated HSDN C3641756 Have diarrhea C0032966 Complication, neoplastic pregnancy HSDN C0700078 Deep tendon reflex decrease C1834659 Muscular dystrophy, limb-girdle, type 1a MalaCards|HPO C0518090 Frequency of pain question C0035066 Renal artery obstruction HSDN C1963184 Nystagmus adverse event C0345382 Gorlin chaudhry moss syndrome OrphaNet C3854173 Pre-renal acute kidney injury C1834567 Myoglobinuria, autosomal dominant MalaCards C2132198 Abnormal blistering of the skin C0268323 Familial porphyria cutanea tarda MalaCards C4085211 Pain distress question C0010414 Infection by cryptococcus neoformans HSDN C0036396 Sciatica C0007222 Cardiovascular diseases HSDN C0237326 Defecation pain C4060572 Chronic functional constipation UMLS C4084775 Usual severity weight loss C0038525 Subarachnoid hemorrhage HSDN C2984058 Have pain C0008373 Cholesteatoma HSDN C1384666 Decreased hearing C0079731 B-cell lymphomas HSDN C0030552 Paralysis partial C0023522 Leukodystrophy, metachromatic OrphaNet|MalaCards C0027796 Neuralgias C0026769 Multiple sclerosis HSDN C0027796 Neuralgias C0003794 Arm injury HSDN C0042963 Symptoms vomiting C0220654 Meningeal carcinomatosis HSDN C0002170 Alopecia disorders C0040100 Thymoma MalaCards C2032395 Pelvic pain on the left C0205788 Histiocytoid hemangioma HSDN C3665492 Pigmentations C0220624 Adult brain tumor MalaCards C0151786 Weakness muscle C0393571 Multiple system atrophy HSDN C0019209 Large liver C0086647 Mucopolysaccharidosis type iiia MalaCards|HPO C4084769 Vomiting frequency C0033778 Vulvar pruritus HSDN C0234132 Pyramidal sign C1837454 Spinocerebellar ataxia 8 MalaCards|HPO|UMLS C0242936 Center pain C1704436 Peripheral arterial diseases HSDN C0036659 Sensation disorder C0007097 Carcinomas HSDN C0042024 Urine incontinence C0038941 Incisional infection HSDN C0034124 Pupillary disorder C0042164 Uveitis HSDN C4084788 Have dizziness C0009240 Cognition HSDN C3641756 Have diarrhea C2945560 Hemolytic HSDN C0242936 Center pain C0038644 Sudden infant death syndrome HSDN C0424755 Fever symptoms C3808991 Congenital disorder of deglycosylation MalaCards C0027796 Neuralgias C0043253 Trauma blunt HSDN C4085549 Dizziness C0013806 Electroplexy shock therapy HSDN C0746674 Muscle weakness generalized C1836448 Nemaline myopathy 1 HPO C0007758 Cerebellar ataxia C0015397 Disorder of eye HSDN C4042891 Sleep wake disorders C0795623 Hepatitis a vaccine, inactivated HSDN C0017181 Gastrointestinal bleed C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0015676 Mental fatigue C0037051 Behavior illness HSDN C2242996 Tingling C0206727 Nerve sheath tumors HSDN C0042928 Paralysis vocal cord C0037369 Smoking HSDN C0022346 Yellow skin C0042216 Poxvirus officinalis HSDN C2096293 Ent surgical result ear vertigo C1546847 Entity name part type - family HSDN C1279888 Proteinuria of undiagnosed cause C4050613 Anxiety scale (basc-2) HSDN C0027796 Neuralgias C0025202 Melanoma HSDN C3539022 Pelvic pain decreasing in severity C0012979 Canine disease HSDN C0025287 Meningitis-like C1510428 Cerebral abscess HSDN C0033774 Skin pruritus C1335042 Non-neoplastic cutaneous disorder UMLS C0042928 Paralysis vocal cord C0002940 Aneurysm HSDN C0013404 Respiratory difficulty C0854973 Stage ii adenosquamous cell carcinoma of lung UMLS C2919142 Short stature adverse event C0431350 Primary microcephaly MalaCards C0000737 Abdomen pain C0015397 Disorder of eye HSDN C0851578 Disorder sleep C0853697 Neutrophil count decreased HSDN C0518090 Frequency of pain question C0000880 Acanthamoeba keratitis HSDN C1963063 Anorexia adverse event C0235387 Porphyria type syndrome OrphaNet C0023530 Leukopenia C0268579 Propionic acidemia HPO C0000737 Abdomen pain C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C0019825 Voice hoarseness C0027344 Nails, malformed HSDN C0011991 Loose stools C0038459 Equine strongyle infection HSDN C0017181 Gastrointestinal bleed C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C4084769 Vomiting frequency C0022423 Judgement HSDN C0042024 Urine incontinence C0017638 Glioma HSDN C4085642 Level of joint stiffness C0032533 Polymyalgia rheumatica MalaCards C0235153 Sensory hallucination C2936779 Hydroxymethylbilane synthase deficiency MalaCards C1384666 Decreased hearing C0012979 Canine disease HSDN C0013404 Respiratory difficulty C0011603 Dermatitis HSDN C2911647 Weight gain adverse event C0002514 Amino acid metabolism, inborn errors HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019187 Hepatitis, alcoholic HSDN C3539889 Pelvic pain increasing in severity C0020517 Hypersensitivity HSDN C2984057 Have nausea C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0010200 Cough symptom C0852007 Scleroderma and associated disorders OrphaNet C4084802 Usual severity diarrhea C4084839 Scabies HSDN C0028738 Nystagmus C0338503 Septo-optic dysplasia OrphaNet|HPO C0004134 Dyssynergia C0027663 Neoplasms, multiple primary HSDN C0015672 Decreased energy C0004045 Asphyxia neonatorum HSDN C0917816 Deficiency mental C2675179 Arginine:glycine amidinotransferase deficiency MalaCards|HPO C3541349 Syncope C0007222 Cardiovascular diseases HSDN C0151311 Cranial nerve palsy C0017671 Glomus jugulare tumor HPO C3815497 Cough C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C2936821 Spinal cerebrospinal fluid leak C0004601 Back injury HSDN C0518090 Frequency of pain question C0079173 Craniomandibular disorders HSDN C0037763 Spasm C0037199 Sinusitis HSDN C1963137 Hydrocephalus adverse event C1846357 Meckel syndrome type 3 HPO C2919142 Short stature adverse event C3469605 Pseudohypoaldosteronism, type iid MalaCards C0013608 Cardiac edema C0600519 Ventricular remodeling HSDN C3539889 Pelvic pain increasing in severity C0563150 Catastrophization HSDN C0575081 Abnormal gait C0752353 Atrophy, muscular, spinobulbar OrphaNet|HPO C0018780 Frequencies hearing high loss C0175702 Williams syndrome HSDN C0030200 Intractable pain C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0518090 Frequency of pain question C0206620 Lymphangioma, cystic HSDN C0424755 Fever symptoms C0276119 Q-fever pneumonia MalaCards C3898969 Have been vomiting C0022729 Klebsiella infections HSDN C4084767 Bothered by vomiting C0339959 Pneumonia chlamydial HSDN C3898969 Have been vomiting C1135868 Gestational trophoblastic neoplasms HSDN C4084726 Distress cough C0032131 Plasmacytoma HSDN C4084766 Vomiting C0043253 Trauma blunt HSDN C0036572 Convulsion C3890167 Mental retardation, x-linked 100 MalaCards|UMLS C0221150 Odynophagia C0006849 Oral candidiasis UMLS C1961131 Cough adverse event C0017107 Gas poison HSDN C0030193 Sense of pain C0853971 Inflammatory carcinoma of breast stage iii UMLS C1961131 Cough adverse event C0020437 Hypercalcemia HSDN C2237041 Shox gene with short stature C0342284 Bangstad syndrome OrphaNet|MalaCards C0038506 Stutter C0033906 Psychological theories HSDN C1090821 Sepsis C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0032326 Pneumothorax HSDN C0018681 Headache, cephalalgia C0031099 Periodontitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0023798 Lipoma HSDN C0917816 Deficiency mental C0268364 Marfanoid mental retardation syndrome MalaCards C4084767 Bothered by vomiting C0022821 Kyphosis deformity of spine HSDN C4085317 Diarrhea frequency C0018273 Growth disorders HSDN C0002963 Angina variant C0242698 Ventricular dysfunction, left HSDN C3641756 Have diarrhea C1837028 Severe combined immunodeficiency, autosomal recessive, t cell negative, b cell positive, nk cell positive HPO C2016108 Overreaction to real or imagined slights or failures C0020517 Hypersensitivity UMLS C1963170 Hypothermia adverse event C0039128 Syphilis HSDN C0150055 Pain chronic C0040136 Thyroid neoplasm HSDN C0041667 Low weight C1849158 Insulin-like growth factor i, resistance to, due to increased binding protein HPO C0853945 Oral mucosa blister C1851573 Transient bullous dermolysis of the newborn OrphaNet|HPO C0013404 Respiratory difficulty C1879591 Lung adenocarcinoma with mixed bronchioloalveolar and invasive components UMLS C4085211 Pain distress question C0206681 Adenocarcinoma, clear cell HSDN C0241137 Skin pallor C0019050 Hemoglobinuria, paroxysmal MalaCards C0015402 Hemorrhage eye C0042161 Uveal diseases HSDN C0043094 Weight gain C0003969 Ascorbic acid deficiency HSDN C4084769 Vomiting frequency C0038013 Ankylosing spondylitis HSDN C0518090 Frequency of pain question C0024473 Magnesium deficiency HSDN C0003469 Anxiety disorder C0012236 Digeorge syndrome MalaCards|HPO C0042963 Symptoms vomiting C0035309 Retinal diseases HSDN C3887638 Failure to thrive in infant C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C0031911 Pigment deposition C0750935 Astrocytoma, cerebral MalaCards C0011991 Loose stools C0267658 Diarrhea caused by alcohol intake UMLS C3641756 Have diarrhea C0398788 Immunodeficiency syndrome, variable MalaCards|HPO C2242996 Tingling C0007222 Cardiovascular diseases HSDN C0349489 Fetal hypoxia C0162494 Pregnancy complications, parasitic HSDN C0027497 Queasy C0020523 Immediate hypersensitivity HSDN C0041834 Erythematous condition C0343056 Acute generalized pustular psoriasis MalaCards C0030975 Disorders perception C0233629 Thinking and speaking disturbances HSDN C0011168 Disorder deglutition C0079136 Cockayne-touraine disease MalaCards C4084769 Vomiting frequency C0265673 Congenital kyphosis HSDN C0030794 Pelvis pain C0458219 Complex regional pain syndromes HSDN C0424755 Fever symptoms C0549160 North asian tick fever nos DiseaseOntology|MalaCards C0034150 Skin purpura C0398597 Histiocytic syndrome HSDN C2203646 Jaundice C1304456 Congo hemorrhagic fever MalaCards C0234428 Consciousness disturbance C0009792 Consciousness disorder UMLS C0030193 Sense of pain C0035793 Rocky mountain spotted fever HSDN C2315100 Pediatric failure to thrive C1855101 Methylmalonyl-coa epimerase deficiency with sepiapterin reductase deficiency HPO C0040034 Thrombocytopenia C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards C0030232 Color loss C0014356 Enterocolitis HSDN C0015672 Decreased energy C0031099 Periodontitis HSDN C4085210 Usual severity pain C0010633 Cystadenoma HSDN C2237041 Shox gene with short stature C3891449 Peeling skin syndrome 1 MalaCards C0241137 Skin pallor C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C0036572 Convulsion C0334582 Fibrillary astrocytoma UMLS C2911647 Weight gain adverse event C0018802 Congestive heart failure HSDN C0042024 Urine incontinence C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C4085862 Bothered by nausea C0022373 Disease, jejunal HSDN C1963093 Dizziness adverse event C1962958 Hematoma adverse event HSDN C0016199 Pain flank C1266043 Sarcomatoid renal cell carcinoma UMLS C0518090 Frequency of pain question C0017178 Gastrointestinal diseases HSDN C4084776 Weight loss C0042035 Urination disorders HSDN C4084774 Have weight loss C0038941 Incisional infection HSDN C0917816 Deficiency mental C3553637 Hyperphosphatasia with mental retardation syndrome 2 MalaCards C0242936 Center pain C2827407 Infectious otitis media HSDN C0042963 Symptoms vomiting C2981667 Stage iib distal bile duct cancer UMLS C0022346 Yellow skin C3810185 Anemia, congenital dyserythropoietic, type ib UMLS C0001707 Aerophagia C0027651 Tumor HSDN C0033774 Skin pruritus C0748226 Radial neuropathy HSDN C0002962 Angina C0001721 Emotional affect HSDN C0023014 Developmental disorder language C0023055 Laryngeal neoplasm HSDN C4084726 Distress cough C0268250 Gaucher disease, type 2 (disorder) OrphaNet|HPO|MalaCards C0344315 Mood depressed C0025268 Multiple endocrine neoplasia type 2a OrphaNet C4084784 Diarrhea C0086438 Hypogammaglobulinemia OrphaNet|MalaCards C4085211 Pain distress question C0009081 Congenital clubfoot HSDN C3463815 Feel fatigue C0042373 Vascular diseases HSDN C4084775 Usual severity weight loss C0001418 Adenocarcinoma HSDN C0018777 Deafness, conductive C1550639 Specimen type - fistula HSDN C0020455 Hypergammaglobulinemia C1458155 Mammary neoplasms HSDN C2919142 Short stature adverse event C1859359 Camptodactyly syndrome, guadalajara type i OrphaNet|MalaCards C2984057 Have nausea C0037929 Spinal cord injuries HSDN C0042571 Vertigo subjective C0029118 Opportunistic infections HSDN C0522224 Palsied C0008354 Cholera HSDN C0332573 Macula C0282687 Hemorrhagic fever, ebola MalaCards C0015970 Fever unknown origin C0030567 Parkinson disease HSDN C4084776 Weight loss C0242287 Isaacs syndrome OrphaNet|MalaCards C0011991 Loose stools C0085178 Needle stick injury HSDN C2911647 Weight gain adverse event C0034885 Rectal neoplasms HSDN C3814778 Hemolytic index C0037054 Sickle cell trait MalaCards C0030193 Sense of pain C0007462 Causalgia syndrome UMLS C0270948 Neurogenic muscular atrophy C1850625 Native american myopathy MalaCards|HPO C4085862 Bothered by nausea C0018794 Heart block HSDN C0426579 Anorexia symptom C0018790 Cardiac arrest HSDN C0007758 Cerebellar ataxia C1412084 Abcd1 gene HSDN C0019572 Hairiness C0796124 Proud syndrome HPO C4084776 Weight loss C0221036 Acrodermatitis enteropathica HPO C0151786 Weakness muscle C0004114 Astrocytoma HSDN C1279888 Proteinuria of undiagnosed cause C0403556 Glomerulopathy, familial lobular MalaCards C0009806 Constipate C0400839 Ulcer rectal UMLS C0018681 Headache, cephalalgia C0018824 Heart valve disease HSDN C0019572 Hairiness C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0518090 Frequency of pain question C0019114 Hemosiderosis HSDN C0270844 Convulsions tonic C0270855 Early myoclonic encephalopathy MalaCards C0234428 Consciousness disturbance C0206667 Adrenal cortical adenoma MalaCards C0242936 Center pain C0003615 Appendicitis MalaCards C4084724 Usual severity constipation C4041080 Neurocognitive disorders HSDN C1557397 Adverse event associated with pain C0302182 Trabecular adenocarcinoma MalaCards C0000737 Abdomen pain C1853297 Maturity-onset diabetes of the young, type 8, with exocrine dysfunction HPO|UMLS C0241210 Speaking delay C3150925 Spastic ataxia 4, autosomal recessive HPO C4084766 Vomiting C0033953 Psychosexual disorders HSDN C4042891 Sleep wake disorders C0005695 Bladder neoplasm HSDN C3829611 Nausea frequency C0007125 Carcinoma, ehrlich tumor HSDN C1963281 Vomiting adverse event C0020621 Hypokalemia HSDN C2919142 Short stature adverse event C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards|HPO C0030193 Sense of pain C0038354 Stomach diseases HSDN C0018524 Hallucinate C0029882 Otitis media HSDN C0151786 Weakness muscle C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0040460 Dental pain C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0030193 Sense of pain C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C2911645 Weight loss adverse event C0042131 Uterine diseases HSDN C1963091 Diarrhea adverse event C0037199 Sinusitis HSDN C2126170 Sore on left side of mouth C0149745 Oral ulcer UMLS C0024032 Birth weight subnormal C1839125 Say-meyer syndrome MalaCards C0234512 Prosopagnosia C0752347 Lewy body disease HSDN C0031911 Pigment deposition C0079218 Fibromatosis, aggressive MalaCards C4084767 Bothered by vomiting C0018273 Growth disorders HSDN C4084727 Cough frequency C0036341 Schizophrenia HSDN C3854481 Vomiting, infantile C0014356 Enterocolitis MalaCards C0152459 Striae C0011609 Drug eruptions HSDN C4084726 Distress cough C0001969 Alcoholic intoxication HSDN C4084723 Constipation C0270726 Alexander disease OrphaNet|MalaCards C0231835 Respiration rate increased C2937225 Biotin deficiency disease MalaCards C3665347 Vision impaired C2936826 Fumaric aciduria MalaCards|HPO C0557874 Global developmental delay C0795940 Filippi syndrome MalaCards C0018772 Deafness C0014118 Endocarditis HSDN C0020505 Excessive eating C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0577567 Mass of urogenital structure C0156397 Vulval hematoma UMLS C1557397 Adverse event associated with pain C0085271 Self-injurious behavior HSDN C1963071 Back pain adverse event C0018188 Granuloma HSDN C1279888 Proteinuria of undiagnosed cause C0019159 Hepatitis a HSDN C0035078 Failure kidney C1527406 Rhizomelic pseudopolyarthritis MalaCards C3887638 Failure to thrive in infant C1855849 Bartter syndrome, antenatal , type 2 HPO C0042510 Fibrillation paroxysmal vent C3501836 Long qt syndrome 3-6 MalaCards C0018772 Deafness C3489393 Hiatal hernia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024694 Mandibular neoplasms HSDN C0454644 Delayed language development C3151462 Mental retardation, autosomal recessive 14 MalaCards C4084774 Have weight loss C0009241 Cognition disorders HSDN C0557874 Global developmental delay C0035078 Kidney failure MalaCards C0424755 Fever symptoms C0018946 Hematoma, subdural HSDN C0151889 Reflexes tendon increased C1842836 Congenital disorder of glycosylation, type ii MalaCards|HPO C0011991 Loose stools C0015734 Stool impacted HSDN C0917816 Deficiency mental C0795949 Galloway mowat syndrome HPO C0460137 Push down or depress C0162532 Variegate porphyria MalaCards|HPO C0518090 Frequency of pain question C0033117 Priapism HSDN C0035229 Respiratory function impaired C1857492 Craniosynostosis with fibular aplasia OrphaNet|MalaCards C4084802 Usual severity diarrhea C0038160 Staphylococcal infections HSDN C0751093 Dystonia, limb C1414216 Dystonia 6, torsion (disorder) MalaCards|HPO C1963087 Constipation adverse event C0036983 Septic shock HSDN C0587246 Extremity weakness C0026896 Myasthenia gravis MalaCards C0019209 Large liver C1881600 Malignant vipoma MalaCards C0032617 High urine output C0026865 Mushroom poisoning HSDN C1579931 Depressed - symptom C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0020627 Hypopharyngeal neoplasms HSDN C4084802 Usual severity diarrhea C0007177 Cardiac tamponade HSDN C4084727 Cough frequency C0014859 Esophageal neoplasms OrphaNet|HSDN|MalaCards C0233794 Memory impaired C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy OrphaNet|HPO C0036572 Convulsion C0393728 Decision making epilepsy UMLS C4084769 Vomiting frequency C0027643 Neoplasm recurrence, local HSDN C0518090 Frequency of pain question C0043515 Zollinger-ellison syndrome HSDN C0026826 High muscle tone C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C3887638 Failure to thrive in infant C0268285 Adrenal hyperplasia, congenital, type 5 HPO C0034933 Abnormal reflexes C0001418 Adenocarcinoma HSDN C0333422 Gumma C0276007 Gummata and ulcers of yaws UMLS C0007398 Catatonic C0027927 Neurosyphilis HSDN C3887638 Failure to thrive in infant C1858328 Bile acid synthesis defect, congenital, 4 MalaCards|HPO C0034933 Abnormal reflexes C0027927 Neurosyphilis HSDN C0020649 Blood pressure decreased C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C1963086 Confusion adverse event C0038663 Suicide attempt HSDN C1549543 Administration method - pain C0019421 Heterosexual behavior HSDN C0019209 Large liver C0026948 Mycosis fungoides MalaCards C0030554 Abnormal sensation C0013990 Pathological accumulation of air in tissues HSDN C0038002 Spleen enlargement C3279664 Emberger syndrome MalaCards C0042571 Vertigo subjective C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C0009421 Comatose C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C2984058 Have pain C0029434 Osteogenesis imperfecta HSDN C0003862 Pain joint C0019069 Hemophilia a MalaCards C0086437 Joint hypermobility C1833603 Spondyloepiphyseal dysplasia with atlantoaxial instability MalaCards C0018524 Hallucinate C1963229 Retinal detachment adverse event HSDN C4085548 Usual severity dizziness C0152054 Therapeutic touch HSDN C0009421 Comatose C0268418 Deficiency of glycerol kinase MalaCards|HPO C0020578 Hyperventilate C0014549 Tonic-clonic epilepsy HSDN C0030554 Abnormal sensation C0038356 Stomach neoplasms HSDN C1963252 Tremor adverse event C0677866 Brain stem neoplasms HSDN C0020458 Hyperhydrosis C0040021 Thromboangiitis obliterans MalaCards C4085211 Pain distress question C0021345 Infectious mononucleosis HSDN C0497406 Over weight C0559260 Congenital scoliosis HSDN C0424755 Fever symptoms C0032964 Pregnancy complications, hematologic HSDN C2984058 Have pain C0019021 Hemoglobin c disease HSDN C4084769 Vomiting frequency C0024117 Chronic obstructive airway disease HSDN C1971624 Appetite absent C0043121 Wernicke encephalopathy HSDN C4084788 Have dizziness C0032371 Poliomyelitis HSDN C1963071 Back pain adverse event C1546654 Specimen source codes - granuloma HSDN C0017181 Gastrointestinal bleed C1260903 Dysfibrinogenemia MalaCards C0151889 Reflexes tendon increased C3888031 Spinocerebellar ataxia 35 MalaCards C0233565 Bradykinesia C0376329 New variant creutzfeldt-jakob disease MalaCards C0042963 Symptoms vomiting C1636667 Disorder characterized by eosinophilia HSDN C2024893 Cardiovascular surgery result: fatigue C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C0015469 Facial paralysis C0017636 Glioblastoma HSDN C0002962 Angina C0010034 Corneal diseases HSDN C0012833 Dizzy C0004933 Behavior modification technique HSDN C1962976 Ventricular fibrillation adverse event C1843738 Long qt syndrome 1, acquired, susceptibility to HPO C0018772 Deafness C1854698 Multiple carboxylase deficiency, juvenile-onset OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0018843 Heat stroke HSDN C1549543 Administration method - pain C0043124 West nile fever HSDN C0027796 Neuralgias C0030271 Pancoast syndrome HSDN C0031911 Pigment deposition C0007137 Squamous cell carcinoma MalaCards C0025287 Meningitis-like C0006818 Campylobacter infection HSDN C1549543 Administration method - pain C1412084 Abcd1 gene HSDN C0040822 D tremors C0031117 Peripheral neuropathy HSDN C2984058 Have pain C0040435 Tooth diseases HSDN C4085211 Pain distress question C1412004 Tumor of the pineal region HSDN C0026821 Cramp C1847896 Charcot-marie-tooth disease, dominant intermediate a MalaCards|UMLS C0030193 Sense of pain C0149678 Epstein-barr virus infections HSDN C0020578 Hyperventilate C0005491 Biofeedback HSDN C0030486 Extremity paralysis, lower C0035801 Diseases rodent HSDN C0030214 Myoclonus palatal C0151532 Disorder brain stem UMLS C0039070 Collapse fleeting C1336537 Supratentorial meningioma MalaCards C0577560 Eye mass C0266561 Congenital cyst of posterior segment of eye UMLS C1963091 Diarrhea adverse event C0038271 Stereotyped behavior HSDN C0151889 Reflexes tendon increased C0036161 Sandhoff disease HPO C0015469 Facial paralysis C0027932 Neurotic disorders HSDN C3641755 Have constipation C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C0015469 Facial paralysis C0162820 Dermatitis, allergic contact HSDN C4084774 Have weight loss C1691228 Cystic kidney diseases HSDN C0015672 Decreased energy C0007932 Chagas' disease + no organ inv DiseaseOntology C0231528 Muscle pain generalized C0039984 Thoracic outlet syndrome OrphaNet|MalaCards C0011168 Disorder deglutition C2678415 Hyperphenylalaninemia, bh4-deficient, due to partial pts deficiency HPO C0042940 Disorder of voice C0003467 Anxiety HSDN C2984058 Have pain C0043253 Trauma blunt HSDN C0015672 Decreased energy C2936881 Eosinophilic synovitis MalaCards C2315100 Pediatric failure to thrive C0019343 Pemphigoid gestationis OrphaNet|MalaCards C4085210 Usual severity pain C0028431 Acquired nasal deformities HSDN C1963281 Vomiting adverse event C0008074 Child development disorders, pervasive HSDN C0024031 Back pain lower back C0009240 Cognition HSDN C2242996 Tingling C0014859 Esophageal neoplasms HSDN C0013378 Dysgensia C0007117 Basal cell carcinoma HSDN C0020615 Hypoglycemia nos C1864948 Hyperinsulinemic hypoglycemia, familial, 4 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0032285 Pneumonia HSDN C0040034 Thrombocytopenia C3645711 Congenital osteopetrosis MalaCards C0018808 Murmur C0014859 Esophageal neoplasms HSDN C1963281 Vomiting adverse event C0022758 Kap HSDN C2919142 Short stature adverse event C3553571 Congenital disorder of glycosylation, type iik MalaCards C4084766 Vomiting C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C1963137 Hydrocephalus adverse event C1866130 Rhombencephalosynapsis OrphaNet|MalaCards C0018681 Headache, cephalalgia C2112207 Post-endarterectomy headache UMLS C0020673 Hypothermia (central) (local) C1579931 Depressed - symptom HSDN C0030552 Paralysis partial C0011644 Scleroderma OrphaNet|MalaCards C0015672 Decreased energy C0001623 Adrenal gland hypofunction HSDN C0751295 Memory loss or impairment C0004943 Behcet syndrome MalaCards|HPO C1963281 Vomiting adverse event C0038587 Substance withdrawal syndrome HSDN C0151786 Weakness muscle C0014061 Tick-borne encephalitis HSDN C0010038 Corneal opacity disorder C1852555 Corneal endothelial dystrophy 1, autosomal dominant MalaCards C4020887 Photodysphoria C2931795 Chromosome 11, deletion 11p OrphaNet C2237041 Shox gene with short stature C2931008 Congenital disorder of glycosylation type 2a MalaCards|HPO C0009806 Constipate C0018934 Hematocolpos HSDN C0030552 Paralysis partial C0149931 Migraine disorders HSDN C2984058 Have pain C0010308 Congenital hypothyroidism HSDN C0860603 Anxiety symptom C0085292 Stiff-person syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0003950 Ascariasis HSDN C3539895 Pelvic pain occurs with bowel movement C0314657 Genetic predisposition HSDN C0030232 Color loss C0272126 Evans syndrome OrphaNet|MalaCards C0009460 Communication impairment C0018674 Head trauma HSDN C0917816 Deficiency mental C2931391 Cataract mental retardation anal atresia urinary defects OrphaNet|MalaCards C4085211 Pain distress question C0027962 Melanocytic nevus HSDN C4085862 Bothered by nausea C2020541 Strabismus HSDN C4084723 Constipation C0038478 Struma ovarii HSDN C0036572 Convulsion C4040739 3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome MalaCards C1962956 Flatulence adverse event C0023903 Liver neoplasms HSDN C0080233 Dental loss C0406715 Fried tooth and nail syndrome MalaCards C0002962 Angina C1704212 Embolism embolus HSDN C3539895 Pelvic pain occurs with bowel movement C0025202 Melanoma HSDN C1557397 Adverse event associated with pain C0023465 Acute monocytic leukemia HSDN C0027796 Neuralgias C0040435 Tooth diseases HSDN C0040259 Tinea pedis C0275522 Infection subclinical HSDN C0344435 Ventricular fibrillation by ecg finding C2748542 Cardiac conduction defect, nonspecific (disorder) HPO C3887638 Failure to thrive in infant C0795956 Chylomicron retention disease OrphaNet|HPO|MalaCards C0878773 Bladder hyperactive C0460137 Push down or depress HSDN C0042025 Urinary incontinence stress C0003469 Anxiety disorders HSDN C0028738 Nystagmus C3887937 Cone dystrophy 5, x-linked MalaCards C1963170 Hypothermia adverse event C0038395 Streptococcal infections HSDN C4084725 Usual severity cough C0032227 Pleural effusion disorder HSDN C3274924 Have been coughing C2937421 Prostatic hyperplasia HSDN C0221263 Cafe au lait spot C0015397 Disorder of eye HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0021847 Intestinal pseudo-obstruction HSDN C3463815 Feel fatigue C0033046 Premenstrual syndrome HSDN C0018777 Deafness, conductive C0406727 Orofaciodigital syndrome 4 MalaCards C3665386 Abnormal vision C0265301 Sclerosteosis HPO C0030193 Sense of pain C0030569 Secondary parkinson disease HSDN C0023015 Language handicap C3281137 Chromosome 17q12 duplication syndrome MalaCards C3887638 Failure to thrive in infant C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C0009676 Confusion state C0001726 Affective symptoms HSDN C1963281 Vomiting adverse event C0019151 Hepatic encephalopathy HSDN C0037036 Increased salivation C3151056 Spastic paraplegia 51, autosomal recessive MalaCards|HPO C1963091 Diarrhea adverse event C0038941 Incisional infection HSDN C0030552 Paralysis partial C1090821 Sepsis (invertebrate) HSDN C0495462 Neonatal difficulty in feeding at breast C0554614 Other perinatal conditions UMLS C0017672 Pain tongue C0039336 Gustatory sense HSDN C1557397 Adverse event associated with pain C0027661 Neoplasms, hormone-dependent HSDN C0041657 Consciousness loss C0003811 Cardiac arrhythmia HSDN C2024893 Cardiovascular surgery result: fatigue C1962976 Ventricular fibrillation adverse event HSDN C4084897 Sleep disturbance subordinate domain C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C1963091 Diarrhea adverse event C0021361 Female infertility HSDN C0007859 Pain neck C0033968 Psychotherapeutic technique HSDN C0235162 Difficult sleeping C1836706 Hyperthyroidism, nonautoimmune UMLS C2096293 Ent surgical result ear vertigo C0037188 Sinoatrial block HSDN C0011168 Disorder deglutition C1853723 Myopathy, distal 2 MalaCards|HPO C0042025 Urinary incontinence stress C0013080 Down syndrome HSDN C1565249 Limitation, mobility C0748540 Scleroderma, limited HSDN C4085658 Usual severity lack of appetite C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C0030193 Sense of pain C0035066 Renal artery obstruction HSDN C3539892 Pelvic pain in front C0026857 Musculoskeletal diseases HSDN C0151908 Dry skin C0162809 Kallmann syndrome HPO C4085210 Usual severity pain C0036986 Shock, traumatic HSDN C0375562 Abdominal or pelvic swelling, mass, or lump, epigastric C0810319 Other and unspecified gastrointestinal disorders UMLS C0026838 Spasticity muscle C1835614 Hereditary hyperexplexia MalaCards C4085211 Pain distress question C0158570 Vascular anomaly HSDN C0476273 Distress respiratory C1970456 Surfactant metabolism dysfunction, pulmonary, 3 MalaCards|HPO C3887873 Hearing loss C0040427 Tooth abnormalities HSDN C0332573 Macula C0018553 Hamartoma syndrome, multiple OrphaNet|HPO|MalaCards C0426579 Anorexia symptom C0334409 Leydig cell tumor, benign HSDN C0857305 Thrombocytopenia purpura C0007621 Neoplastic cell transformation HSDN C1557397 Adverse event associated with pain C0027794 Neural tube defects HSDN C0424755 Fever symptoms C0031117 Peripheral neuropathy HSDN C0522224 Palsied C1258666 Myxoid cyst HSDN C3887638 Failure to thrive in infant C0345893 Juvenile polyposis syndrome HPO C2024878 Cardiovascular surgery result: dyspnea C0018800 Cardiomegaly HSDN C1963064 Anxiety adverse event C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0009080 Finger clubbing C1838163 Osler-rendu-weber syndrome 2 MalaCards|HPO C0026826 High muscle tone C0220669 Familial benign neonatal epilepsy OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0042487 Venous thrombosis HSDN C4084725 Usual severity cough C0029408 Degenerative polyarthritis HSDN C0086565 Liver function abnormal C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C4084774 Have weight loss C0279607 Adult primary hepatocellular carcinoma MalaCards C0007758 Cerebellar ataxia C0752166 Bardet-biedl syndrome HPO C0151827 Pain eye C0268483 Tyrosinemias HSDN C4085222 Nausea C0009319 Colitis HSDN C0242936 Center pain C0037322 Active eye movement sleep HSDN C0028738 Nystagmus C3809221 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 MalaCards C0002170 Alopecia disorders C1857069 Schopf-schulz-passarge syndrome (disorder) OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0406740 Kohlschutter tonz syndrome OrphaNet|UMLS|HPO|MalaCards C0015672 Decreased energy C0003486 Aortic aneurysm HSDN C0009806 Constipate C2240378 Cleft palate on exam HSDN C0018524 Hallucinate C0439840 Reflex motion descriptor HSDN C0231807 Dyspnea exertional C1850635 Atrial myxoma, familial MalaCards C3539022 Pelvic pain decreasing in severity C2706915 Language:-:point in time:^patient:- HSDN C0497247 Blood pressure elevation C0031190 Persistent fetal circulation syndrome HPO C1963249 Tinnitus adverse event C0001430 Adenoma HSDN C0349588 Stature short C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C4084727 Cough frequency C0011616 Contact dermatitis HSDN C0014591 Bleeding nose C3279756 Hermansky-pudlak syndrome 7 MalaCards C0149651 Clubbing C0282207 Cronkhite-canada syndrome MalaCards C0424755 Fever symptoms C0020758 Congenital ichthyosis HSDN C0012569 Double vision C0003873 Rheumatoid arthritis HSDN C2237041 Shox gene with short stature C0079588 Ichthyosis, x-linked MalaCards C0040822 D tremors C0019202 Hepatolenticular degeneration MalaCards|HPO|UMLS C0022346 Yellow skin C2706915 Language:-:point in time:^patient:- HSDN C4084784 Diarrhea C0019294 Hernia, inguinal HSDN C4085211 Pain distress question C0024143 Lupus nephritis HSDN C0012766 Skin sensation disturbance C0030554 Paresthesia UMLS C0013404 Respiratory difficulty C2350530 Bronchopulmonary aspergillosis HSDN C0023014 Developmental disorder language C0037286 Skin neoplasms HSDN C0751495 Seizure focal C0085543 Epilepsia partialis continua UMLS C1963281 Vomiting adverse event C1704212 Embolism embolus HSDN C1384666 Decreased hearing C0796095 Opitz trigonocephaly syndrome MalaCards C0020505 Excessive eating C0022661 Kidney failure, chronic HSDN C0424755 Fever symptoms C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards|HPO C0027497 Queasy C0861861 Squamous cell bile duct carcinoma UMLS C0011991 Loose stools C0997768 Glaucoma HSDN C3274924 Have been coughing C0023092 Lassa fever OrphaNet|MalaCards C0018524 Hallucinate C0023467 Leukemia, myelocytic, acute HSDN C0012833 Dizzy C0017160 Gastroenteritis HSDN C2984057 Have nausea C0038354 Stomach diseases HSDN C0162285 Edema eyelid C4048800 Telomeric 22q13 monosomy syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C0950122 Frasier syndrome MalaCards C0023380 Lethargy C0011263 Multi-infarct dementia UMLS C4049602 Hyperactivity C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO C2032151 Bilateral leg pain C4047626 Pain co-occurrent and due to varicose veins of bilateral legs UMLS C0557874 Global developmental delay C0220742 Bixler christian gorlin syndrome MalaCards C0700078 Deep tendon reflex decrease C1853710 Hereditary motor and sensory neuropathy, type iic (disorder) MalaCards|HPO C1963065 Apnea adverse event C0878544 Cardiomyopathies HSDN C0013421 Dystonia C0795949 Galloway mowat syndrome HPO C0035229 Respiratory function impaired C0039263 Takayasu arteritis MalaCards C1557397 Adverse event associated with pain C0026683 Mucocele HSDN C0234132 Pyramidal sign C2677565 Amyotrophic lateral sclerosis 10 (disorder) UMLS C0853986 Lymphocytes decreased C0009447 Common variable immunodeficiency OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C3812171 Bradycardia by ecg finding HSDN C0022346 Yellow skin C0021361 Female infertility HSDN C0020305 Fetal edema C0019693 Hiv infections HSDN C2024893 Cardiovascular surgery result: fatigue C0027092 Myopia HSDN C0011991 Loose stools C0014394 Enuresis HSDN C0030193 Sense of pain C2711099 Chronic pain, psychogenic UMLS C0004134 Dyssynergia C0011168 Deglutition disorders HSDN C0015672 Decreased energy C0034734 Raynaud disease HSDN C0018772 Deafness C0022610 Kernicterus HSDN C0005745 Blepharoptosis C1834523 Arthrogryposis, distal, type 2b OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0009782 Connective tissue diseases HSDN C4084802 Usual severity diarrhea C0149931 Migraine disorders HSDN C1963170 Hypothermia adverse event C1704272 Benign prostatic hyperplasia HSDN C0007758 Cerebellar ataxia C0027819 Neuroblastoma MalaCards|HSDN C2024878 Cardiovascular surgery result: dyspnea C0032290 Aspiration pneumonia HSDN C0010200 Cough symptom C0796561 Melanoma vaccines HSDN C2242996 Tingling C2239112 Blister dosing unit HSDN C3898969 Have been vomiting C0030330 Panniculitis, peritoneal HSDN C4084776 Weight loss C1321581 Bezoar disorder HSDN C0040264 Ear ringing sound C0024305 Lymphoma, non-hodgkin HSDN C0917816 Deficiency mental C1852750 Coloboma, uveal, with cleft lip and palate and mental retardation HPO C4020887 Photodysphoria C1275074 Odonto-onycho-dermal dysplasia MalaCards C0018772 Deafness C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C0019572 Hairiness C1720862 Congenital generalized lipodystrophy type 1 MalaCards|HPO C0234533 Seizure generalized C3151853 Mcleod syndrome with chronic granulomatous disease HPO C2096293 Ent surgical result ear vertigo C0008350 Cholelithiasis HSDN C0184567 Pain acute C0524528 Pervasive development disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0040962 Tricuspid valve prolapse HSDN C0020538 Hbp C3839212 Familial hyperaldosteronism type 2 MalaCards C0151205 Periorbital edema C1720864 Sulfatidosis, juvenile, austin type MalaCards|HPO C1963184 Nystagmus adverse event C0751039 Cockayne syndrome, type i HPO C0151740 Intracranial hypertension C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0035435 Rheumatism HSDN C4085642 Level of joint stiffness C1968748 Gangliosidosis, generalized gm1, type i, with cardiac involvement HPO C4084768 Usual severity vomiting C1510412 Pseudoaneurysm HSDN C0038990 Sweats C1851479 Keratoderma palmoplantaris transgrediens OrphaNet C0009676 Confusion state C1000483 Genus anemia HSDN C0030193 Sense of pain C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0728710 Pupil constriction observed C0015310 Exotropia HSDN C1963137 Hydrocephalus adverse event C0023788 Whipple disease MalaCards C1961131 Cough adverse event C0149514 Bronchitis acute MalaCards C1963184 Nystagmus adverse event C0041409 Turner syndrome, male MalaCards C0026826 High muscle tone C0021295 Infant, premature, diseases HSDN C0851578 Disorder sleep C0009651 Conditioning operant HSDN C1260880 Nasal drip C1707964 Exophytic schneiderian papilloma UMLS C2029884 Hearing loss by exam C1962963 Osteoporosis adverse event HSDN C0015672 Decreased energy C0015300 Exophthalmos HSDN C3274924 Have been coughing C1304456 Congo hemorrhagic fever MalaCards C0000731 Abdomen distention C1867774 Sacral agenesis syndrome HPO C4085661 Usual severity nausea C0023798 Lipoma HSDN C4085549 Dizziness C0014836 Escherichia coli infections HSDN C1963091 Diarrhea adverse event C0037929 Spinal cord injuries HSDN C2030274 Heavy bleeding between periods C1882229 Ovarian thecoma MalaCards C0033774 Skin pruritus C0242188 Spider bites HSDN C4085317 Diarrhea frequency C0031142 Peritoneal diseases HSDN C4085211 Pain distress question C0025490 Mesonephroma HSDN C1549543 Administration method - pain C0014100 Endarteritis, nos HSDN C3887638 Failure to thrive in infant C2675184 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis MalaCards|HPO C0234523 Apraxia, classic C0042830 Perception visual HSDN C2187990 Unable to perform sex C0349604 Intracranial meningioma MalaCards C0022346 Yellow skin C1860808 Triosephosphate isomerase deficiency UMLS C4084775 Usual severity weight loss C1956390 Cranial arteritis MalaCards C1557397 Adverse event associated with pain C1253937 Pericardial effusion HSDN C3463815 Feel fatigue C3542413 Cdisc adas-cog - comprehension HSDN C2096293 Ent surgical result ear vertigo C0011849 Diabetes mellitus HSDN C1145670 Failure respiratory C1739094 Foodborne botulism MalaCards C2984058 Have pain C0034012 Delayed puberty HSDN C0027498 Nausea vomiting C0023827 Liposarcoma MalaCards C0162298 Stiffness joints C0344490 Sacral agenesis OrphaNet|HPO C4084784 Diarrhea C0037354 Smallpox HSDN C1963281 Vomiting adverse event C3714514 Infection HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017661 Iga glomerulonephritis HSDN C0003862 Pain joint C0011644 Scleroderma OrphaNet|MalaCards C0042963 Symptoms vomiting C0011981 Diaphragmatic eventration HSDN C0575081 Abnormal gait C1968746 Gangliosidosis, generalized gm1, late-infantile type HPO C0036572 Convulsion C1853623 Fryns-aftimos syndrome MalaCards C0424755 Fever symptoms C0005659 Bite sting HSDN C0917816 Deficiency mental C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0030552 Paralysis partial C0020517 Hypersensitivity HSDN C0150055 Pain chronic C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C3463815 Feel fatigue C2963140 Arteriovenous fistula in use with two needles HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0080233 Tooth loss HSDN C0037036 Increased salivation C3280479 Pitt-hopkins-like syndrome 2 MalaCards C0023015 Language handicap C0394016 Coma, post-head injury HSDN C4085317 Diarrhea frequency C3150207 Agammaglobulinemia 6, autosomal recessive HPO C0002965 Crescendo angina C0013295 Duodenal ulcer HSDN C0242936 Center pain C0038862 Inflammation purulent HSDN C0015732 Feces incontinence C2678194 Mental retardation, x-linked, syndromic, christianson type HPO C0151740 Intracranial hypertension C0025149 Medulloblastoma MalaCards C1519353 Skin eruption papular C1833030 Palmoplantar keratoderma, nonepidermolytic OrphaNet|HPO|MalaCards C0155552 Hearing loss mixed C0024021 Loudness perception HSDN C0522224 Palsied C0040411 Tongue neoplasms HSDN C0033774 Skin pruritus C0032463 Polycythemia vera HPO C0020458 Hyperhydrosis C0206042 Fatal familial insomnia HPO C0009421 Comatose C0038356 Stomach neoplasms HSDN C2700617 Irritation - emotion C3280766 Joubert syndrome 14 MalaCards C0042571 Vertigo subjective C0305062 Tetanus toxoids HSDN C0037036 Increased salivation C3713418 Ppm-x syndrome MalaCards C0151908 Dry skin C0796093 Odontoonychodermal dysplasia MalaCards|HPO C0009806 Constipate C3146252 Stage ii colorectal cancer ajcc v7 UMLS C2984058 Have pain C0018816 Heart septal defects HSDN C3539892 Pelvic pain in front C0042063 Urogenital abnormalities HSDN C0917816 Deficiency mental C0032339 Rothmund-thomson syndrome MalaCards|HPO C0018524 Hallucinate C1548578 Location characteristic id - smoking HSDN C1962972 Proteinuria adverse event C0020523 Immediate hypersensitivity HSDN C0003550 Broca aphasia C0014549 Tonic-clonic epilepsy HSDN C2911645 Weight loss adverse event C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C1963170 Hypothermia adverse event C0041755 Adverse reaction to drug HSDN C0019079 Bloody sputum C0018915 Hemangioendothelioma HSDN C0007758 Cerebellar ataxia C1838570 Ceroid lipofuscinosis, neuronal, 8 MalaCards|HPO C0020578 Hyperventilate C0425045 Sudden infant death HSDN C3665347 Vision impaired C0022797 Adult neuronal ceroid lipofuscinosis MalaCards C2024878 Cardiovascular surgery result: dyspnea C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0010200 Cough symptom C0014854 Esophageal diverticulum HSDN C1963091 Diarrhea adverse event C0007125 Carcinoma, ehrlich tumor HSDN C4085317 Diarrhea frequency C0027686 Pathologic neovascularization HSDN C1557397 Adverse event associated with pain C0001849 Aids dementia complex HSDN C2984057 Have nausea C0039590 Testicular neoplasms HSDN C3898969 Have been vomiting C0024143 Lupus nephritis HSDN C4084774 Have weight loss C0024299 Lymphoma HSDN C0278134 Anesthesias C0162309 Adrenoleukodystrophy MalaCards|UMLS C4084773 Bothered by weight gain C0029445 Bone necrosis HSDN C3539892 Pelvic pain in front C0206630 Endometrial stromal sarcoma HSDN C1963249 Tinnitus adverse event C0042138 Uterine neoplasms HSDN C0018681 Headache, cephalalgia C0205833 Medullomyoblastoma UMLS C4085661 Usual severity nausea C0015457 Expression facial HSDN C0022346 Yellow skin C0281361 Adenocarcinoma of pancreas UMLS C0030486 Extremity paralysis, lower C0038661 Suicide HSDN C0011991 Loose stools C0086650 Mps iii d HPO|UMLS C1999266 Depression adverse event C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C3665347 Vision impaired C1838644 Stargardt disease 3 MalaCards C0031911 Pigment deposition C0023827 Liposarcoma MalaCards C1963252 Tremor adverse event C1302282 Chromaffin cell neoplasm MalaCards C0011991 Loose stools C0030521 Parathyroid neoplasms HSDN C0036572 Convulsion C2931727 Chromosome 10 ring OrphaNet|MalaCards C0424755 Fever symptoms C0205788 Histiocytoid hemangioma HSDN C0237849 Skin desquamation C0026948 Mycosis fungoides MalaCards C3665386 Abnormal vision C1970848 Phosphoglycerate kinase 1 deficiency MalaCards|HPO C1971624 Appetite absent C0035435 Rheumatism HSDN C2096293 Ent surgical result ear vertigo C0030567 Parkinson disease HSDN C0017181 Gastrointestinal bleed C0398641 Epstein syndrome (disorder) HPO C4085661 Usual severity nausea C1961100 Erectile dysfunction adverse event HSDN C0003079 Pupillary inequality C1565107 Disorder, secondary headache HSDN C2315100 Pediatric failure to thrive C0268242 Niemann-pick disease, type a MalaCards|HPO C1384666 Decreased hearing C0002986 Fabry disease OrphaNet|HSDN|MalaCards C4084774 Have weight loss C0032914 Pre-eclampsia HSDN C4084775 Usual severity weight loss C0021890 Intraoperative complications HSDN C4084774 Have weight loss C0024894 Mastitis HSDN C0036572 Convulsion C0751254 Creutzfeldt-jakob disease, familial MalaCards C0013604 Edematous C0001624 Adrenal gland neoplasms HSDN C1557397 Adverse event associated with pain C0032326 Pneumothorax HSDN C0005745 Blepharoptosis C1862264 Bpes with duane retraction syndrome HPO C1963252 Tremor adverse event C2745996 Fitzsimmons syndrome MalaCards C4085211 Pain distress question C1145670 Respiratory failure HSDN C0454644 Delayed language development C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C3641756 Have diarrhea C0004589 B. anthracis HSDN C0851578 Disorder sleep C0162429 Malnutrition HSDN C0020673 Hypothermia (central) (local) C1334928 Necrotic changes (finding) HSDN C1557397 Adverse event associated with pain C0014055 Encephalitis, epidemic HSDN C0270790 Quadriparesis C0812437 Oculo-dento-digital syndrome MalaCards|HPO|UMLS C1963091 Diarrhea adverse event C0032045 Placenta disorders HSDN C3815497 Cough C0018024 Goiter, retrosternal HSDN C2032396 Pelvic pain on the right C0010692 Cystitis HSDN C3641756 Have diarrhea C3150751 Agammaglobulinemia 3, autosomal recessive HPO C0518090 Frequency of pain question C0085315 Toxoplasmosis, cerebral HSDN C0917816 Deficiency mental C0221356 Brachycephaly MalaCards|HPO C1549543 Administration method - pain C0037859 Spermatocele HSDN C0242936 Center pain C0017417 Genital neoplasms, male HSDN C0151603 Edema generalized C0272258 Cryoglobulinemia, primary MalaCards C4085317 Diarrhea frequency C0585274 Periodic syndrome OrphaNet|HPO C3539896 Pelvic pain occurs with urination C0019310 Hernia, obturator HSDN C4084774 Have weight loss C0700208 Acquired scoliosis HSDN C0151825 Ostalgia C1292769 Precursor b-cell lymphoblastic leukemia UMLS C0042510 Fibrillation paroxysmal vent C2748542 Cardiac conduction defect, nonspecific (disorder) HPO C1963249 Tinnitus adverse event C0086543 Cataract nos HSDN C4084773 Bothered by weight gain C0017661 Iga glomerulonephritis HSDN C2315100 Pediatric failure to thrive C3150801 Combined oxidative phosphorylation deficiency 7 MalaCards|HPO C4084767 Bothered by vomiting C0021831 Intestinal diseases HSDN C1069915 Vertigo C0042029 Urinary tract infection HSDN C0917816 Deficiency mental C2673375 Mucolipidosis iii alpha beta, atypical HPO C0015300 Ocular proptosis C0265374 Warfarin syndrome MalaCards C2984058 Have pain C0006109 Brain damage, chronic HSDN C0242936 Center pain C0029001 Onchocerciasis HSDN C3539022 Pelvic pain decreasing in severity C0001418 Adenocarcinoma HSDN C0018681 Headache, cephalalgia C0011882 Diabetic neuropathies HSDN C0476250 Head neck mass C0339136 Cyst; lacrimal apparatus UMLS C3665386 Abnormal vision C0032533 Polymyalgia rheumatica MalaCards C0033377 Caudal displacement C1832812 Cataracts, congenital, with sensorineural deafness, down syndrome-like facial appearance, short stature, and mental retardation HPO C0030552 Paralysis partial C1855255 Pseudoarylsulfatase a deficiency MalaCards C0027796 Neuralgias C0038436 Post-traumatic stress disorder HSDN C0039070 Collapse fleeting C0026946 Mycoses HSDN C3641756 Have diarrhea C0014761 Erythroblastosis, fetal HSDN C0085636 Light sensitivity C0026654 Moyamoya disease HSDN C0086565 Liver function abnormal C1855861 Glycogen storage disease 0, liver MalaCards C4084788 Have dizziness C1414203 Dws gene HSDN C4084776 Weight loss C0003507 Aortic valve stenosis HSDN C0424755 Fever symptoms C3554540 Lymphoproliferative syndrome 2 MalaCards C0018681 Headache, cephalalgia C0017636 Glioblastoma MalaCards|HSDN|UMLS C0242936 Center pain C0006433 Burnout, professional HSDN C0003811 Cardiac rhythm disturbance C2676137 Diamond-blackfan anemia 1 MalaCards C0023380 Lethargy C1547940 Specimen source codes - ulcer HSDN C3665347 Vision impaired C2020284 Stickler syndrome, type 1 MalaCards|HPO C0013604 Edematous C1719313 Hereditary amyloid nephropathy MalaCards C0085642 Asphyxia reticularis C0344311 Blister HSDN C1549543 Administration method - pain C0036920 Sezary syndrome HSDN C0008031 Pain chest C2706915 Language:-:point in time:^patient:- HSDN C0000727 Abdomen acute C0242188 Spider bites HSDN C0522224 Palsied C0009244 Behavioral cognitive therapy HSDN C0518090 Frequency of pain question C0014805 Primary erythermalgia HPO C3641756 Have diarrhea C0007138 Carcinoma, transitional cell HSDN C0043094 Weight gain C0029408 Degenerative polyarthritis HSDN C0018784 Deafness sensorineural C0027902 Neuropsychological diagnosis HSDN C4084768 Usual severity vomiting C0021831 Intestinal diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C0002895 Anemia, sickle cell HSDN C4084769 Vomiting frequency C0029928 Ovarian diseases HSDN C3539889 Pelvic pain increasing in severity C0038160 Staphylococcal infections HSDN C1963086 Confusion adverse event C1623041 Breast-fed HSDN C4085222 Nausea C0018671 Head and neck neoplasms HSDN C0022638 Ketosis C1848793 Tiglic acidemia MalaCards C0040485 Wryneck C0518450 Spinal fractures HSDN C4084767 Bothered by vomiting C0032987 Ectopic pregnancy HSDN C4085210 Usual severity pain C0015558 Fallopian tube neoplasms HSDN C2237041 Shox gene with short stature C0044707 11 beta hsd HPO C1549543 Administration method - pain C0237935 Trust HSDN C0015970 Fever unknown origin C0149678 Epstein-barr virus infections HSDN C0518090 Frequency of pain question C0027070 Myoepithelioma HSDN C4085317 Diarrhea frequency C0001125 Acidosis, lactic HSDN C0085636 Light sensitivity C0017601 Glaucomas HSDN C0013362 Dysarthrias C0016952 Galactosemias MalaCards C0040822 D tremors C0027849 Neuroleptic malignant syndrome HSDN C4084775 Usual severity weight loss C0014474 Ependymoma HSDN C1860844 Sparse, thin hair C2931026 Choroidal atrophy alopecia OrphaNet|MalaCards C0015469 Facial paralysis C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C1557397 Adverse event associated with pain C0001144 Acne vulgaris HSDN C0042963 Symptoms vomiting C0019151 Hepatic encephalopathy HSDN C2919142 Short stature adverse event C0342284 Bangstad syndrome OrphaNet|MalaCards C1999266 Depression adverse event C2931859 Acquired cjd MalaCards C0036572 Convulsion C0025037 Meckel diverticulum HSDN C0030193 Sense of pain C0002991 Cutaneous fibrous histiocytoma HSDN C0019825 Voice hoarseness C0011581 Depressive disorder HSDN C0151825 Ostalgia C0029454 Osteopetrosis OrphaNet|MalaCards C2315100 Pediatric failure to thrive C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards C0038002 Spleen enlargement C0023473 Myeloid leukemia, chronic OrphaNet|HPO C4085317 Diarrhea frequency C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C4085661 Usual severity nausea C0302497 Retrobulbar haemorrhage HSDN C0034150 Skin purpura C0151436 Vasculitis, leukocytoclastic, cutaneous OrphaNet|MalaCards C4084774 Have weight loss C0023904 Liver neoplasms, experimental HSDN C0242936 Center pain C0003466 Anus, imperforate HSDN C0030193 Sense of pain C0023465 Acute monocytic leukemia HSDN C0030486 Extremity paralysis, lower C0003855 Arteriovenous fistula HSDN C0003467 Angst C0271097 Usher syndrome MalaCards C0518090 Frequency of pain question C0039483 Giant cell arteritis HSDN C0027497 Queasy C0018621 Hay fever HSDN C0008031 Pain chest C1704272 Benign prostatic hyperplasia HSDN C0851578 Disorder sleep C0023434 Chronic lymphocytic leukemia HSDN C0020672 Body temperature decreased C0042826 Field visual HSDN C1557397 Adverse event associated with pain C0020097 Htlv-i infections HSDN C4085317 Diarrhea frequency C0004275 Attitude health HSDN C1557397 Adverse event associated with pain C0040137 Thyroid nodule HSDN C0234253 Rest pain C3650235 Atherosclerosis of an autologous bypass graft of extremities with rest pain UMLS C2096293 Ent surgical result ear vertigo C0032463 Polycythemia vera OrphaNet|HPO C2029884 Hearing loss by exam C0001126 Renal tubular acidosis HSDN C0038990 Sweats C0005859 Bloom syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0085435 Arthritis, reactive MalaCards|HSDN C4084774 Have weight loss C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0018681 Headache, cephalalgia C3662853 Allergic migraine UMLS C4084725 Usual severity cough C1963083 Cholecystitis adverse event HSDN C0557874 Global developmental delay C0917800 Epilepsy, myoclonic, infantile OrphaNet|MalaCards C0015469 Facial paralysis C0024299 Lymphoma HSDN C0086565 Liver function abnormal C2931004 Congenital disorder of glycosylation type 1j MalaCards C0242936 Center pain C0041834 Erythema HSDN C3815497 Cough C0003873 Rheumatoid arthritis HSDN C0018681 Headache, cephalalgia C0038941 Incisional infection HSDN C0028738 Nystagmus C2677500 Oculoauricular syndrome MalaCards|HPO C0042963 Symptoms vomiting C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0009676 Confusion state C1623041 Breast-fed HSDN C0030193 Sense of pain C1334277 Infiltrating ductal and lobular carcinoma UMLS C0042928 Paralysis vocal cord C0016548 Foreign body migration HSDN C4084802 Usual severity diarrhea C0018824 Heart valve disease HSDN C2984058 Have pain C0004030 Aspergillosis HSDN C0522224 Palsied C0039841 Thiamine deficiency HSDN C0522224 Palsied C0027819 Neuroblastoma HSDN C2132198 Abnormal blistering of the skin C0030805 Bullous pemphigoid OrphaNet|HPO|MalaCards C0023014 Developmental disorder language C2117329 X-ray of toe: polydactyly HSDN C0022346 Yellow skin C1333308 Carcinoma of distal biliary tract UMLS C4085210 Usual severity pain C0019156 Hepatic veno-occlusive disease HSDN C0184567 Pain acute C0009492 Compartment syndromes HSDN C0030486 Extremity paralysis, lower C0002395 Alzheimer's disease HSDN C0235299 Abdomen ruq pain C0008350 Cholelithiasis UMLS C0518090 Frequency of pain question C3150878 Hyperoxaluria, primary, type iii MalaCards C3539022 Pelvic pain decreasing in severity C1552262 Nurse practitioner - family HSDN C0009806 Constipate C0021364 Male infertility HSDN C0221166 Paraparesis C2697932 Loeys-dietz syndrome HSDN C0151818 Opisthotonos C0555206 Chiari malformation type ii MalaCards|UMLS C0007814 Cerebrospinal fluid otorrhea C0085388 Intracranial tuberculoma HSDN C0018772 Deafness C2751630 Dursun syndrome HPO C0018989 Paresis of one side of body C0268386 Amyloid polyneuropathy, swiss type MalaCards C0013604 Edematous C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0349588 Stature short C1853271 Hypophosphatemic rickets with hypercalciuria, hereditary OrphaNet|HPO C0013362 Dysarthrias C0004135 Ataxia telangiectasia OrphaNet|HSDN|HPO|MalaCards C3815497 Cough C2073625 X-ray of chest: pleural effusion HSDN C1999266 Depression adverse event C0020179 Huntington disease MalaCards|HPO C0042024 Urine incontinence C2931355 Spastic paraplegia 3, autosomal dominant HPO C3274924 Have been coughing C0033873 Psychiatry HSDN C0454644 Delayed language development C1859568 Bardet-biedl syndrome 10 HPO C4084776 Weight loss C0004442 Avoidance learning HSDN C0030554 Abnormal sensation C0752235 Lyme neuroborreliosis MalaCards C4085661 Usual severity nausea C0009450 Disease caused by microorganism HSDN C0424755 Fever symptoms C0011334 Dental caries HSDN C0000737 Abdomen pain C1336261 Ovarian embryonal carcinoma, stage iii UMLS C0037315 Breathing disorder during sleeping C3891556 Chromosome xq26.3 duplication syndrome MalaCards C0030193 Sense of pain C0235146 Emotionally high HSDN C1963087 Constipation adverse event C0233629 Thinking and speaking disturbances HSDN C0018524 Hallucinate C1962979 Burn adverse event HSDN C2130135 Midback pain present upon awakening C3805412 Cataract 41 MalaCards C0003811 Cardiac rhythm disturbance C0079541 Holoprosencephaly MalaCards C4084767 Bothered by vomiting C0035956 Rupture spontaneous HSDN C3898969 Have been vomiting C0037116 Silicosis HSDN C0151798 Liver necrosis C0349535 Carcinoid tumor of intestine MalaCards C4084802 Usual severity diarrhea C0020502 Hyperparathyroidism HSDN C0043068 Friderichsen-waterhouse syndrome C0036982 Shock, hemorrhagic HSDN C1549543 Administration method - pain C0750394 Wbc low HSDN C0000737 Abdomen pain C0085605 Liver failure HSDN C0022346 Yellow skin C0042345 Varicosity HSDN C0013405 Dyspnea, paroxysmal C0006384 Bundle-branch block HSDN C3463815 Feel fatigue C0029396 Heterotopic ossification HSDN C2024878 Cardiovascular surgery result: dyspnea C0042216 Poxvirus officinalis HSDN C4084774 Have weight loss C0001807 Aggressive behavior HSDN C0547030 Sensory perceptual alteration: visual C2986550 Pituicytoma UMLS C0000731 Abdomen distention C2239176 Liver carcinoma MalaCards C0234428 Consciousness disturbance C3146222 Idiopathic aortitis MalaCards C2919142 Short stature adverse event C1867858 Prader-willi syndrome chromosome region HPO C0018524 Hallucinate C0020517 Hypersensitivity HSDN C4084776 Weight loss C0004161 Athletic injuries HSDN C0037317 Sleep disturbance C1970431 Pitt-hopkins syndrome MalaCards C0036572 Convulsion C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards|HPO|UMLS C1069915 Vertigo C0024841 Matrimony, matrimonial HSDN C4085642 Level of joint stiffness C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C0812426 Kidney problem C0027709 Nephrocalcinosis UMLS C0002962 Angina C0040100 Thymoma HSDN C0015469 Facial paralysis C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084767 Bothered by vomiting C0022951 Lactose intolerance HSDN C0009398 Color vision defects C0162809 Kallmann syndrome MalaCards|HPO C2203646 Jaundice C1963119 Stomach ulcer adverse event HSDN C0018772 Deafness C1414529 Fancc gene HPO C0231528 Muscle pain generalized C0004576 Babesiosis OrphaNet|MalaCards C1963281 Vomiting adverse event C0032229 Pleural neoplasms HSDN C3898969 Have been vomiting C1548777 Specimen reject reason - hemolysis HSDN C3898969 Have been vomiting C0020303 Hydropneumothorax HSDN C1963091 Diarrhea adverse event C0424688 Small head HSDN C0086439 Activity decreased C0338430 Limbic encephalitis HSDN C0086437 Joint hypermobility C3809875 Van maldergem syndrome 2 MalaCards|UMLS C0040485 Wryneck C0426784 Rheumatoid; torticollis UMLS C2032395 Pelvic pain on the left C0520720 Cyst nerve root HSDN C2919142 Short stature adverse event C1844696 Otopalatodigital syndrome, type ii MalaCards|HPO C0013604 Edematous C0014038 Encephalitis HSDN C4085548 Usual severity dizziness C0002895 Anemia, sickle cell HSDN C3641756 Have diarrhea C1384607 Food deprivation HSDN C1527344 Dysphonia C0017409 Herpes zoster oticus HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014511 Epithelial cyst HSDN C4085210 Usual severity pain C0024221 Lymphangioma HSDN C2984058 Have pain C0034194 Pyloric stenosis HSDN C4085862 Bothered by nausea C2937287 Hematolysis HSDN C0030193 Sense of pain C3661932 Angina associated with type 2 diabetes mellitus UMLS C4042891 Sleep wake disorders C0014548 Epilepsy, generalized HSDN C1279888 Proteinuria of undiagnosed cause C3496337 Idiopathic nephrotic syndrome MalaCards C0424755 Fever symptoms C0019103 Omsk haemorrhagic fever MalaCards C0085631 Abnormal excitement C0751748 Nonketotic hyperglycinemia MalaCards|HPO C4084769 Vomiting frequency C0264766 Rheumatic mitral stenosis HSDN C0577567 Mass of urogenital structure C1828115 Cancer of ovary, stage 3 UMLS C0019825 Voice hoarseness C0033348 Language program HSDN C0036572 Convulsion C1858114 Huntington disease-like 3 (disorder) MalaCards|UMLS C0040822 D tremors C1857093 Dystonia 2, torsion, autosomal recessive (disorder) MalaCards|HPO|UMLS C0000737 Abdomen pain C0027765 Nervous system disorder HSDN C4085862 Bothered by nausea C1321581 Bezoar disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0010674 Cystic fibrosis HSDN C0155502 Vertigo benign positional C0037313 Sleep HSDN C4084897 Sleep disturbance subordinate domain C1970269 Choreoathetosis, hypothyroidism, and neonatal respiratory distress HPO C0237326 Defecation pain C0035436 Rheumatic fever MalaCards C0018681 Headache, cephalalgia C0020649 Hypotension HSDN C0034933 Abnormal reflexes C0344315 Depressed mood HSDN C0018777 Deafness, conductive C1861848 Paragangliomas 4 MalaCards C1145670 Failure respiratory C0005283 Beta thalassemia OrphaNet C0009806 Constipate C0013985 Emotional disturbances UMLS C3641755 Have constipation C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C1510456 Wernicke aphasia C0036356 Schizophrenics--language HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006157 Breech presentation HSDN C3539896 Pelvic pain occurs with urination C3495422 Finding relating to sexuality and sexual activity HSDN C0013362 Dysarthrias C0040411 Tongue neoplasms HSDN C4085210 Usual severity pain C0030521 Parathyroid neoplasms HSDN C1549543 Administration method - pain C0033999 Pterygium HSDN C3463815 Feel fatigue C0002895 Anemia, sickle cell HSDN C0857305 Thrombocytopenia purpura C0340629 Aortic aneurysm without mention of rupture nos HSDN C0221232 Welts C1304199 Angio-oedema of eyelids UMLS C0013362 Dysarthrias C3150171 Ftld-tdp, tardbp-related HPO C0015469 Facial paralysis C0003864 Arthritis HSDN C0036572 Convulsion C3887898 Infantile spasm UMLS C0030193 Sense of pain C0010418 Cryptosporidiosis HSDN C4084727 Cough frequency C0014858 Esophageal motility disorders HSDN C2315100 Pediatric failure to thrive C0001768 Agammaglobulinemia OrphaNet|MalaCards C0027497 Queasy C0007133 Carcinoma, papillary HSDN C0032617 High urine output C0035579 Rickets HSDN C4084723 Constipation C2751067 Parkinsonism-dystonia, infantile MalaCards|HPO C0851578 Disorder sleep C1847501 Glut1 deficiency syndrome MalaCards C3641891 Have itch C0041228 African trypanosomiasis DiseaseOntology C1961131 Cough adverse event C0497327 Dementia HSDN C2362324 Pediatric obesity C0015579 Family characteristics HSDN C2911645 Weight loss adverse event C0018799 Heart diseases HSDN C1963281 Vomiting adverse event C0011334 Dental caries HSDN C0023530 Leukopenia C2931418 Bare lymphocyte syndrome 2 HPO C3463815 Feel fatigue C1859317 Cataract and cardiomyopathy MalaCards|HPO C0013404 Respiratory difficulty C0029601 Other respiratory abnormalities UMLS C0018772 Deafness C0003962 Ascites HSDN C0036572 Convulsion C3899659 Childhood giant cell glioblastoma UMLS C2919142 Short stature adverse event C0265497 Chromosome xxxxx syndrome OrphaNet|MalaCards C0036572 Convulsion C0009395 Color perception HSDN C0019079 Bloody sputum C1336162 Stage iia large cell carcinoma of lung UMLS C0424755 Fever symptoms C0334533 Arteriovenous hemangioma HSDN C4084769 Vomiting frequency C0004044 Asphyxia HSDN C4084723 Constipation C0007137 Squamous cell carcinoma HSDN C0030552 Paralysis partial C1962976 Ventricular fibrillation adverse event HSDN C0020578 Hyperventilate C3813607 Infantile gastroesophageal reflux HSDN C4084723 Constipation C1546533 Specimen source codes - abscess HSDN C3146279 Coma C0021603 Sleep initiation and maintenance disorders HSDN C4049602 Hyperactivity C2931817 Chromosome 2q37 deletion syndrome MalaCards C4085317 Diarrhea frequency C0042131 Uterine diseases HSDN C0004941 Behavioral symptoms C0268631 Succinic semialdehyde dehydrogenase deficiency OrphaNet|HPO|MalaCards C0242936 Center pain C0403447 Chronic kidney insufficiency HSDN C3274924 Have been coughing C1552527 Clinic / center - developmental disabilities HSDN C0007758 Cerebellar ataxia C1859965 Alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus MalaCards C0020673 Hypothermia (central) (local) C0042487 Venous thrombosis HSDN C0036659 Sensation disorder C0038273 Stereotypic movement disorder HSDN C0030554 Abnormal sensation C0024141 Lupus erythematosus, systemic HSDN C0018681 Headache, cephalalgia C1334685 Medulloblastoma with leptomeningeal spread UMLS C3641756 Have diarrhea C1848590 Vascular hyalinosis MalaCards C0043094 Weight gain C1691215 Penile hypospadias HSDN C0034933 Abnormal reflexes C1999266 Depression adverse event HSDN C0002962 Angina C0026918 Mycobacterium infections HSDN C0030486 Extremity paralysis, lower C0022423 Judgement HSDN C0031911 Pigment deposition C0035334 Retinitis pigmentosa MalaCards C0027066 Myoclonic jerking C0342765 D-glyceric aciduria HPO|UMLS C0042928 Paralysis vocal cord C0037397 Behavior social HSDN C0037763 Spasm C0997768 Glaucoma HSDN C0233514 Behavior abnormal C0033800 Pseudoglioma MalaCards C4084776 Weight loss C0009475 Community mental health service HSDN C2911645 Weight loss adverse event C0042138 Uterine neoplasms HSDN C0007758 Cerebellar ataxia C0017675 Glossitis HSDN C0018834 Brash C1096660 Ehlers-danlos syndrome type ix MalaCards C0454644 Delayed language development C3550904 Epileptic encephalopathy, early infantile, 36 MalaCards C0013604 Edematous C2937287 Hematolysis HSDN C0236078 Scrotum pain C1997249 Neuralgia, pudendal MalaCards C0221752 Rbc urine C0268743 Membranoproliferative glomerulonephritis, type ii MalaCards C0019572 Hairiness C0011860 Diabetes mellitus, non-insulin-dependent HSDN C3829611 Nausea frequency C0021295 Infant, premature, diseases HSDN C4085548 Usual severity dizziness C0025284 Meningeal neoplasms HSDN C0004134 Dyssynergia C0206245 Amyloid neuropathies, familial MalaCards C0003469 Anxiety disorder C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C0035232 Diaphragmatic paralysis C0032827 Potassium deficiency HSDN C0002962 Angina C0006849 Oral candidiasis HSDN C4085661 Usual severity nausea C0023055 Laryngeal neoplasm HSDN C0013604 Edematous C0020456 Hyperglycemia HSDN C0020305 Fetal edema C0268226 Type i mucolipidosis HPO C3829611 Nausea frequency C0033873 Psychiatry HSDN C2203646 Jaundice C0872996 Q fever vaccine HSDN C0006370 Bulimia C0014544 Epilepsy HSDN C4085661 Usual severity nausea C0003507 Aortic valve stenosis HSDN C0002622 Amnesias C0009395 Color perception HSDN C2984057 Have nausea C0030807 Pemphigus, nos HSDN C0015230 Exanthem C0406754 Keratosis pilaris with ichthyosis and deafness UMLS C0042024 Urine incontinence C0030849 Penile neoplasms HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0031212 Personality disorders HSDN C2029884 Hearing loss by exam C0027947 Neutropenia HSDN C3898969 Have been vomiting C0003811 Cardiac arrhythmia HSDN C0018772 Deafness C0027697 Nephritis HSDN C0497406 Over weight C0004626 Pneumonia, bacterial HSDN C2911645 Weight loss adverse event C0001624 Adrenal gland neoplasms HSDN C0010520 Skin cyanosis C0001973 Alcoholic intoxication, chronic HSDN C0018772 Deafness C1859565 Bardet-biedl syndrome 7 HPO C0424755 Fever symptoms C0010246 Coxsackievirus infections HSDN C4084784 Diarrhea C0032320 Peritoneal free air HSDN C0038506 Stutter C0282512 Landau-kleffner syndrome HSDN C0424755 Fever symptoms C1963068 Atrial flutter adverse event HSDN C0042024 Urine incontinence C2984291 Glioblastoma multiforme pathway HSDN C0020580 Decreased sensation C0038016 Spondylolisthesis HSDN C0018681 Headache, cephalalgia C0001624 Adrenal gland neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085082 Fungemia HSDN C4084784 Diarrhea C0039614 Tetanus HSDN C0036572 Convulsion C0270841 Simple partial seizures evolving to complex partial seizures, then to generalized tonic-clonic seizures UMLS C0086437 Joint hypermobility C0022716 Menkes kinky hair syndrome MalaCards|HPO|UMLS C4050613 Anxiety C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C2984058 Have pain C0162834 Hyperpigmentation HSDN C2919142 Short stature adverse event C0162283 Nephrogenic diabetes insipidus HPO C0009421 Comatose C0014544 Epilepsy HSDN C3641756 Have diarrhea C0020615 Hypoglycemia HSDN C0000737 Abdomen pain C1546635 Specimen source codes - fistula HSDN C0013404 Respiratory difficulty C1290398 Cerebral arterial aneurysm HSDN C2984058 Have pain C0041318 Tuberculosis, meningeal HSDN C4085661 Usual severity nausea C1962983 Cataract adverse event HSDN C4084775 Usual severity weight loss C0016542 Foreign body HSDN C0018524 Hallucinate C0011854 Diabetes mellitus, insulin-dependent HSDN C3829611 Nausea frequency C1546635 Specimen source codes - fistula HSDN C0013604 Edematous C0007099 Carcinoma in situ HSDN C0036572 Convulsion C1332288 Anaplastic secondary supratentorial astrocytoma UMLS C0020673 Hypothermia (central) (local) C0007097 Carcinomas HSDN C0042963 Symptoms vomiting C1963088 Cystitis adverse event HSDN C0015469 Facial paralysis C0014544 Epilepsy HSDN C4050613 Anxiety C2931168 Hemangiomas, and cutaneous and intracranial vascular deformations MalaCards C4042891 Sleep wake disorders C0795841 Jacobsen distal 11q deletion syndrome HSDN C0013362 Dysarthrias C3553816 Spinocerebellar ataxia, autosomal recessive 13 MalaCards C3887873 Hearing loss C0262655 Recurrent urinary tract infection HSDN C2911647 Weight gain adverse event C0018809 Heart neoplasm HSDN C0004604 Pain back C0425045 Sudden infant death HSDN C0030552 Paralysis partial C0220998 Hypothalamic hypothyroidism MalaCards C0221170 Stiffness muscle C4011726 Myopathy, tubular aggregate, 1 MalaCards|UMLS C0030794 Pelvis pain C0018965 Hematuria HSDN C3539895 Pelvic pain occurs with bowel movement C0026769 Multiple sclerosis HSDN C0019572 Hairiness C0003469 Anxiety disorders HSDN C4084784 Diarrhea C1961100 Erectile dysfunction adverse event HSDN C0009792 Consciousness disorder C0751739 Basal ganglia cerebrovascular disease HSDN C0040264 Ear ringing sound C0007771 Intracranial arteriosclerosis HSDN C0020649 Blood pressure decreased C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0013395 Indigestion C0021847 Intestinal pseudo-obstruction HSDN C0424755 Fever symptoms C0009187 Coccidiosis HSDN C0004604 Pain back C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia HPO|UMLS C0231218 Malaise generalized C0085762 Alcohol abuse UMLS C1549543 Administration method - pain C0014901 Aesthetic HSDN C0023015 Language handicap C0342257 Complications of diabetes mellitus HSDN C0040264 Ear ringing sound C0024121 Lung neoplasms HSDN C0003962 Ascites C1563715 Andersen syndrome OrphaNet|MalaCards C0020903 Illusion C0344315 Depressed mood HSDN C2984058 Have pain C0027873 Neuromyelitis optica HSDN C3539020 Pelvic pain decreasing in frequency C0242669 Placenta retained HSDN C0000737 Abdomen pain C1266087 Acinar cell cystadenocarcinoma UMLS C0018772 Deafness C1838329 Aplasia cutis congenita with epibulbar dermoids MalaCards C3641755 Have constipation C0022661 Kidney failure, chronic HSDN C0426579 Anorexia symptom C0009940 Convalescence HSDN C0013421 Dystonia C0012746 Dissociative disorder HSDN C0036572 Convulsion C0016751 Hereditary fructose intolerance syndrome HPO|UMLS C0557874 Global developmental delay C2675875 Chromosome 2p16.1 p15 deletion syndrome OrphaNet|MalaCards C0022346 Yellow skin C0162869 Aneurysm, ruptured HSDN C4084726 Distress cough C0007133 Carcinoma, papillary HSDN C0151786 Weakness muscle C2137063 Ent surgical result - speech HSDN C0424755 Fever symptoms C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C0424755 Fever symptoms C0033860 Psoriasis HSDN C1384666 Decreased hearing C1096527 Mosaic trisomy 8 syndrome MalaCards C0035232 Diaphragmatic paralysis C0752090 Autoimmune disease models, nervous system HSDN C0242936 Center pain C0040411 Tongue neoplasms HSDN C0233565 Bradykinesia C1847987 Huntington disease-like 2 MalaCards|HPO|UMLS C4084727 Cough frequency C0043251 Wounds and injuries HSDN C0009421 Comatose C1963137 Hydrocephalus adverse event HSDN C0242936 Center pain C0003646 Aptitude HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0948089 Acute coronary syndrome HSDN C0233514 Behavior abnormal C0220765 Weaver-like syndrome MalaCards|HPO C0030232 Color loss C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C1069915 Vertigo C0005586 Bipolar disorder HSDN C1963249 Tinnitus adverse event C0021400 Influenza HSDN C0476250 Head neck mass C0742078 Mass lesion of brain UMLS C0427055 Face weakness C0221054 Welander distal myopathy HPO C0022346 Yellow skin C0042035 Urination disorders HSDN C0037316 Not enough sleeping C3714514 Infection HSDN C0043094 Weight gain C0040997 Trigeminal neuralgia HSDN C0020538 Hbp C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards|HPO C4085222 Nausea C0043352 Xerostomia HSDN C0234523 Apraxia, classic C0030567 Parkinson disease HSDN C0460137 Push down or depress C3150344 Hyperhomocysteinemia, thrombotic, cbs-related HPO C0013404 Respiratory difficulty C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C0018991 Paralysis one side of body C2984299 Asthma pathway HSDN C2984057 Have nausea C0013473 Eating disorders HSDN C0557874 Global developmental delay C1968550 Mental retardation, x-linked, syndromic 13 MalaCards|HPO C0008031 Pain chest C0220981 Metabolic acidosis HSDN C4084775 Usual severity weight loss C0027794 Neural tube defects HSDN C2024893 Cardiovascular surgery result: fatigue C1963067 Atrial fibrillation adverse event HSDN C2024893 Cardiovascular surgery result: fatigue C0036357 Psychology, schizophrenic HSDN C4085211 Pain distress question C0026918 Mycobacterium infections HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0679360 Foodborne disease HSDN C0007758 Cerebellar ataxia C0265673 Congenital kyphosis HSDN C4084775 Usual severity weight loss C0033873 Psychiatry HSDN C1961131 Cough adverse event C0153413 Malignant neoplasm of upper third of esophagus MalaCards C2711646 Alexia and agraphia present C0001825 Agraphia UMLS C4085317 Diarrhea frequency C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0010200 Cough symptom C0153414 Malignant neoplasm of middle third of esophagus MalaCards C1860844 Sparse, thin hair C0432233 Trichorhinophalangeal dysplasia type i MalaCards|HPO|UMLS C1549543 Administration method - pain C0747533 Peroneal neuropathy HSDN C4085222 Nausea C0037313 Sleep HSDN C3274924 Have been coughing C0917875 Esophageal diverticulosis HSDN C3539891 Pelvic pain to the rear C0003873 Rheumatoid arthritis HSDN C4085862 Bothered by nausea C1963266 Uveitis adverse event HSDN C0042963 Symptoms vomiting C0021228 Variability of individual responses HSDN C0042024 Urine incontinence C0019699 Hiv seropositivity HSDN C0040485 Wryneck C3554415 Arthrogryposis, distal, type 5d MalaCards|UMLS C4085317 Diarrhea frequency C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C4084767 Bothered by vomiting C1835888 Diarrhea 4, malabsorptive, congenital MalaCards|HPO C0012569 Double vision C1334410 Localized primitive neuroectodermal tumor MalaCards C1963086 Confusion adverse event C0276496 Familial alzheimer disease (fad) MalaCards C4084784 Diarrhea C0023364 Leptospirosis HSDN C0036572 Convulsion C1333764 Gastric cronkhite canada polyposis MalaCards C4085548 Usual severity dizziness C0017160 Gastroenteritis HSDN C0013421 Dystonia C0040185 Tibia fracture HSDN C4085222 Nausea C0037929 Spinal cord injuries HSDN C0030486 Extremity paralysis, lower C0282607 Vascular neoplasms HSDN C0011168 Disorder deglutition C3714644 Thymus neoplasms MalaCards C0042024 Urine incontinence C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C4084725 Usual severity cough C0524909 Hepatitis b, chronic HSDN C1860844 Sparse, thin hair C0751038 Cockayne syndrome, type ii HPO C0162835 Hypopigmentation C0079504 Hermanski-pudlak syndrome OrphaNet|MalaCards C0009421 Comatose C0026766 Multiple organ failure HSDN C4084724 Usual severity constipation C0517555 Venous thrombosis after immobility HSDN C0232462 Appetite decrease C1385938 Acanthocephaliasis MalaCards C0426579 Anorexia symptom C2930674 Babesioses, human MalaCards C0162298 Stiffness joints C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0001849 Aids dementia complex HSDN C4084775 Usual severity weight loss C0039971 Thirst HSDN C1549543 Administration method - pain C0020097 Htlv-i infections HSDN C0086565 Liver function abnormal C1970173 Acyl-coa dehydrogenase family, member 9, deficiency of MalaCards|HPO C0023014 Developmental disorder language C0035243 Respiratory tract infections HSDN C0003811 Cardiac rhythm disturbance C1837014 Atrial fibrillation, familial, 3 MalaCards C4085211 Pain distress question C0546952 Congenital facial asymmetry HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019087 Hemorrhagic disorders HSDN C1961131 Cough adverse event C0001973 Alcoholic intoxication, chronic HSDN C0030193 Sense of pain C2187547 Retroperitoneal leiomyosarcoma UMLS C0039870 Leanness C0080233 Tooth loss HSDN C0013421 Dystonia C0042830 Perception visual HSDN C0043094 Weight gain C0233629 Thinking and speaking disturbances HSDN C3641755 Have constipation C0025269 Multiple endocrine neoplasia type 2b HSDN|HPO C0004604 Pain back C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0037763 Spasm C0013473 Eating disorders HSDN C3714552 Strength decreased C2931347 Cardiac form of generalized glycogenosis MalaCards C0262527 Intermittent abdominal pain C1849322 Sandhoff disease, infantile type HPO C2029884 Hearing loss by exam C0007134 Renal cell carcinoma HSDN C3641756 Have diarrhea C0018021 Goiter HSDN C0036572 Convulsion C0162672 Merrf syndrome MalaCards|HPO|UMLS C0036572 Convulsion C0029445 Bone necrosis HSDN C0700072 Encounter due to stillbirth C1968603 Osteopetrosis, autosomal recessive 5 HPO C0270790 Quadriparesis C1842563 Heterotopia, periventricular, autosomal recessive HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C3658267 Prostatic neoplasms, castration-resistant HSDN C0030552 Paralysis partial C0009319 Colitis HSDN C0015300 Ocular proptosis C0011989 Camurati-engelmann syndrome MalaCards|HPO C4085211 Pain distress question C0041755 Adverse reaction to drug HSDN C0019825 Voice hoarseness C0005716 Blastomycosis HSDN C2984057 Have nausea C0349464 Wernicke-korsakoff syndrome HSDN C0003113 Anomia C1704972 Genomic orientation HSDN C0002622 Amnesias C0149931 Migraine disorders HSDN C4084802 Usual severity diarrhea C0206247 Amyloid neuropathies MalaCards C0036572 Convulsion C0162309 Adrenoleukodystrophy MalaCards|HPO|UMLS C0020305 Fetal edema C0021828 Intestinal atresia HSDN C0007758 Cerebellar ataxia C1848519 Waardenburg syndrome, type 4a MalaCards|HPO C0000737 Abdomen pain C0014852 Esophageal diseases HSDN C3274924 Have been coughing C0009651 Conditioning operant HSDN C0221752 Rbc urine C1854336 Paragangliomas 3 MalaCards C0151889 Reflexes tendon increased C0751434 Classical phenylketonuria MalaCards|HPO C2911647 Weight gain adverse event C0042875 Vitamin e deficiency HSDN C3898969 Have been vomiting C2586211 Thrombosis of blood vessel HSDN C1557397 Adverse event associated with pain C1504665 Products used to treat diabetic ketoacidosis HSDN C0034150 Skin purpura C0004352 Autistic disorder HSDN C4084725 Usual severity cough C0014118 Endocarditis HSDN C2984058 Have pain C0033845 Pseudotumor cerebri HSDN C4085211 Pain distress question C0001621 Adrenal gland diseases HSDN C0041105 Jaw spasm C0027531 Neck injury HSDN C3641756 Have diarrhea C0000771 Abnormalities, drug induced HSDN C0015468 Face pain C0015461 Facial neoplasms HSDN C0025287 Meningitis-like C0024299 Lymphoma HSDN C4084802 Usual severity diarrhea C0036330 Schistosomiasis mansoni DiseaseOntology C3887638 Failure to thrive in infant C1865373 Severe combined immunodeficiency, partial HPO C0012833 Dizzy C0474820 Glomerocytoma tympanicum HSDN C0030193 Sense of pain C0007781 Intracranial embolism and thrombosis HSDN C4042891 Sleep wake disorders C0026769 Multiple sclerosis HSDN C1963093 Dizziness adverse event C0039239 Sinus tachycardia HSDN C0851578 Disorder sleep C0009946 Conversion disorder HSDN C1963091 Diarrhea adverse event C0026636 Mouth diseases HSDN C1549543 Administration method - pain C0041188 Pyomyositis, tropical HSDN C0041834 Erythematous condition C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C4084726 Distress cough C0020676 Hypothyroidism HSDN C2029884 Hearing loss by exam C2586211 Thrombosis of blood vessel HSDN C0013362 Dysarthrias C3553661 Cerebellar ataxia, nonprogressive, with mental retardation MalaCards C0413252 Hypothermia due to exposure C2239176 Liver carcinoma HSDN C0850758 Pain pelvic C0034065 Pulmonary embolism HSDN C2911645 Weight loss adverse event C0162871 Aortic aneurysm, abdominal HSDN C4084727 Cough frequency C0344434 Atrial fibrillation ecg HSDN C0581394 Lower extremity swelling C0149871 Deep vein thrombosis UMLS C0221263 Cafe au lait spot C0342543 Precocious puberty, central MalaCards C0237326 Defecation pain C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0011991 Loose stools C0004161 Athletic injuries HSDN C3815497 Cough C0026857 Musculoskeletal diseases HSDN C1963184 Nystagmus adverse event C1866425 Yemenite deaf-blind hypopigmentation syndrome MalaCards C0518090 Frequency of pain question C0023281 Leishmaniasis HSDN C0027497 Queasy C0278599 Cns tumor, childhood infratentorial ependymoma UMLS C3541349 Syncope C0085096 Peripheral vascular diseases HSDN C0004134 Dyssynergia C4049644 Depression HSDN C4084769 Vomiting frequency C0314657 Genetic predisposition HSDN C0518090 Frequency of pain question C0013928 Fat embolism HSDN C4084726 Distress cough C0021841 Intestinal neoplasms HSDN C1145670 Failure respiratory C0220748 Cartilage-hair hypoplasia OrphaNet|HPO|MalaCards C0003113 Anomia C0011551 Depersonalisation HSDN C2911647 Weight gain adverse event C0011071 Sudden death HSDN C4084768 Usual severity vomiting C0162871 Aortic aneurysm, abdominal HSDN C0026858 Musculoskeletal pain C0684743 Malignant neoplasm of muscle HSDN C0043094 Weight gain C0021841 Intestinal neoplasms HSDN C3815497 Cough C0751552 Malignant neoplasm of thymus MalaCards C1963087 Constipation adverse event C3150705 Foxg1 syndrome HPO C4084767 Bothered by vomiting C0042214 Vaccinia HSDN C4085548 Usual severity dizziness C0014511 Epithelial cyst HSDN C4085661 Usual severity nausea C0040479 Torsades de pointes HSDN C0027066 Myoclonic jerking C0003469 Anxiety disorders HSDN C2032396 Pelvic pain on the right C0022410 Joint instability HSDN C4085210 Usual severity pain C0949691 Spondylarthropathies HSDN C0039070 Collapse fleeting C0026590 Child mother relationship HSDN C1549543 Administration method - pain C0752143 Intracranial thrombosis HSDN C0011991 Loose stools C0040046 Thrombophlebitis HSDN C0000737 Abdomen pain C1167736 Small intestine cancer stage ii UMLS C3539895 Pelvic pain occurs with bowel movement C0014179 Endometritis HSDN C0151786 Weakness muscle C0458219 Complex regional pain syndromes HSDN C1519353 Skin eruption papular C0580181 Benign lymphocytic infiltration of jessner OrphaNet C4084727 Cough frequency C0034088 Pulmonary valve insufficiency HSDN C2187990 Unable to perform sex C0032001 Pituitary apoplexy OrphaNet|MalaCards C0026821 Cramp C0460137 Push down or depress HSDN C0522224 Palsied C0003873 Rheumatoid arthritis HSDN C3641756 Have diarrhea C0004933 Behavior modification technique HSDN C0398650 Idiopathic thrombocytopenia purpura C0011570 Mental depression HSDN C0036572 Convulsion C3275471 Mental retardation, x-linked, syndromic, chudley-schwartz type MalaCards|UMLS C0349588 Stature short C2931247 Chromosome 17, trisomy 17q22 OrphaNet|MalaCards C1963252 Tremor adverse event C0037397 Behavior social HSDN C4084768 Usual severity vomiting C1416865 Lipa gene HPO C0022346 Yellow skin C0019163 Hepatitis b DiseaseOntology|MalaCards C0036572 Convulsion C1266184 Atypical teratoid/rhabdoid tumor MalaCards C0242936 Center pain C1561518 Pleasure - animals raised for recreation HSDN C0023380 Lethargy C0268060 Juvenile hemochromatosis OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0344434 Atrial fibrillation ecg HSDN C4084766 Vomiting C0268525 5-oxoprolinase deficiency MalaCards|HPO C1971624 Appetite absent C0001349 Acute-phase reaction HSDN C4084767 Bothered by vomiting C0025202 Melanoma HSDN C0242936 Center pain C0013312 Dupuytren contracture HSDN C3829611 Nausea frequency C0853697 Neutrophil count decreased HSDN C1963137 Hydrocephalus adverse event C1864436 Muenke syndrome MalaCards|HPO C0015402 Hemorrhage eye C0085399 Ehrlichiosis HSDN C0011991 Loose stools C1522133 High cholesterol level HSDN C0522224 Palsied C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C1546847 Entity name part type - family HSDN C2242996 Tingling C1274879 Port-wine stain with oculocutaneous melanosis OrphaNet|MalaCards C2237041 Shox gene with short stature C0018553 Hamartoma syndrome, multiple MalaCards|HPO C0019209 Large liver C2931585 Gaucher-like disease MalaCards C0013362 Dysarthrias C0011854 Diabetes mellitus, insulin-dependent HSDN C0011168 Disorder deglutition C0018854 Gamma-chain disease MalaCards C0013604 Edematous C0034152 Henoch-schoenlein purpura MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1290398 Cerebral arterial aneurysm HSDN C2096293 Ent surgical result ear vertigo C0013080 Down syndrome HSDN C0557874 Global developmental delay C0342708 Gamma aminobutyric acid transaminase deficiency MalaCards|HPO C0576456 Poor feeding C3810055 Combined oxidative phosphorylation deficiency 19 MalaCards C0557874 Global developmental delay C0018523 Hallervorden-spatz syndrome MalaCards|HPO C4084768 Usual severity vomiting C0023176 Lead poisoning MalaCards C0917816 Deficiency mental C0085576 Iron-refractory iron deficiency anemia OrphaNet|HPO|MalaCards C0005779 Clotting C2931008 Congenital disorder of glycosylation type 2a MalaCards C1963274 Vasculitis adverse event C4049638 Cutaneous small vessel vasculitis MalaCards C1963063 Anorexia adverse event C0162283 Nephrogenic diabetes insipidus OrphaNet|HPO C4084723 Constipation C0525042 Feeding and eating disorders of childhood HSDN C4084727 Cough frequency C0007570 Celiac disease HSDN C0232466 Feeding difficulty C0175702 Williams syndrome MalaCards C3641756 Have diarrhea C0238124 Necrotizing fasciitis HSDN C0040460 Dental pain C0011581 Depressive disorder HSDN C3463815 Feel fatigue C0023890 Liver cirrhosis HSDN C3641755 Have constipation C0041582 Ulcer HSDN C1963091 Diarrhea adverse event C0524909 Hepatitis b, chronic HSDN C0025287 Meningitis-like C0023518 Leukocytosis UMLS C0027497 Queasy C0677866 Brain stem neoplasms HSDN C0018772 Deafness C0162316 Iron deficiency anemia HSDN C0085593 Chill C0746158 Lung lll pneumonia UMLS C0022346 Yellow skin C1090821 Sepsis (invertebrate) HSDN C0026821 Cramp C0022665 Kidney neoplasm HSDN C4084766 Vomiting C2937287 Hematolysis HSDN C0027796 Neuralgias C0039336 Gustatory sense HSDN C2096293 Ent surgical result ear vertigo C0003469 Anxiety disorders HSDN C0242936 Center pain C0596263 Carcinogenesis HSDN C1963090 Dehydration adverse event C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C4084776 Weight loss C0018799 Heart diseases HSDN C4084775 Usual severity weight loss C0020732 Iatrogenic disease HSDN C0034933 Abnormal reflexes C0009088 Cluster headache HSDN C1279888 Proteinuria of undiagnosed cause C0014761 Erythroblastosis, fetal HSDN C0221166 Paraparesis C0021308 Infarction HSDN C0750426 Wbc elevated C1959626 Mevalonic aciduria MalaCards|HPO C0040822 D tremors C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0005745 Blepharoptosis C0796202 Wittwer syndrome MalaCards C0022346 Yellow skin C1962983 Cataract adverse event HSDN C0009398 Color vision defects C0007785 Cerebral infarction HSDN C0522224 Palsied C0023760 Lip diseases HSDN C4085222 Nausea C0035309 Retinal diseases HSDN C0018681 Headache, cephalalgia C0432272 Van buchem disease MalaCards|HPO C1963281 Vomiting adverse event C2711266 Infection by anisakis larva HSDN C0015468 Face pain C0042769 Virus diseases HSDN C3541349 Syncope C1963215 Pneumothorax adverse event HSDN C0018775 Hearing loss bilateral C0029896 Disease, ent HSDN C0019521 Hiccoughs C0162526 Aids-related opportunistic infections HSDN C0002622 Amnesias C0003486 Aortic aneurysm HSDN C0231528 Muscle pain generalized C0085399 Ehrlichiosis DiseaseOntology|MalaCards C1963091 Diarrhea adverse event C0027660 Neoplasms, glandular and epithelial HSDN C4084775 Usual severity weight loss C0034929 Reflex HSDN C0518090 Frequency of pain question C0037005 Shoulder dislocation HSDN C0036572 Convulsion C2750805 Chromosome 5p13 duplication syndrome MalaCards C4084769 Vomiting frequency C0151526 Premature birth HSDN C1557397 Adverse event associated with pain C0033999 Pterygium HSDN C4084769 Vomiting frequency C0268568 Classic maple syrup urine disease HPO C0030552 Paralysis partial C2675528 Spastic paraplegia 42, autosomal dominant MalaCards|HPO C0018681 Headache, cephalalgia C0039236 Tachycardia episodic HSDN C0020672 Body temperature decreased C0037933 Spinal diseases HSDN C0018772 Deafness C0025345 Menstruation disturbances HSDN C1145670 Failure respiratory C0011633 Dermatomyositis OrphaNet|MalaCards C4085211 Pain distress question C0005398 Cholestasis, extrahepatic HSDN C0002622 Amnesias C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C2984058 Have pain C0026654 Moyamoya disease HSDN C0020672 Body temperature decreased C0005586 Bipolar disorder HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0007570 Celiac disease HSDN C1510456 Wernicke aphasia C0002395 Alzheimer's disease HSDN C0013362 Dysarthrias C2931356 Spastic paraplegia type 5a, recessive MalaCards C2024893 Cardiovascular surgery result: fatigue C0677838 Grief loss HSDN C0518090 Frequency of pain question C0029001 Onchocerciasis HSDN C0019209 Large liver C0011989 Camurati-engelmann syndrome MalaCards|HPO C0042571 Vertigo subjective C0597109 Nurse's role HSDN C1962956 Flatulence adverse event C1384606 Dyspareunia HSDN C0042571 Vertigo subjective C0032343 Poisoning HSDN C0030552 Paralysis partial C4084909 Depression subordinate domain HSDN C0022346 Yellow skin C3151147 Bile acid synthesis defect, congenital, 3 OrphaNet|UMLS|HPO|MalaCards C0020673 Hypothermia (central) (local) C0524851 Neurodegenerative disorders HSDN C2024893 Cardiovascular surgery result: fatigue C0026771 Trauma multiple HSDN C0522224 Palsied C0042932 Animal vocalizations HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0011644 Scleroderma OrphaNet|MalaCards C0013604 Edematous C0036421 Systemic scleroderma OrphaNet|MalaCards C0030193 Sense of pain C1333162 Cranial nodular fasciitis UMLS C1145670 Failure respiratory C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0232466 Feeding difficulty C1868619 Paramyotonia congenita without cold paralysis HPO C0010520 Skin cyanosis C0002792 Anaphylaxis HSDN C4085210 Usual severity pain C0031212 Personality disorders HSDN C0015672 Decreased energy C0032064 Plague HSDN C1000483 Genus anemia C0265965 Dyskeratosis congenita OrphaNet|HPO|MalaCards C3665386 Abnormal vision C0043324 Juvenile xanthogranuloma MalaCards C4084769 Vomiting frequency C1962986 Glaucoma adverse event HSDN C0015672 Decreased energy C1709574 Pleural epithelioid mesothelioma UMLS C3887784 Decreased urine output C4084909 Depression subordinate domain HSDN C0014591 Bleeding nose C0272317 Hereditary factor ii deficiency disease HPO C0025323 Bleeding menstrual heavy C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C3463815 Feel fatigue C0041582 Ulcer HSDN C4085222 Nausea C0011570 Mental depression HSDN C1963091 Diarrhea adverse event C0362046 Prediabetes syndrome HSDN C0004134 Dyssynergia C0040188 Tic disorder HSDN C3539889 Pelvic pain increasing in severity C0041954 Ureteral diseases and syndromes HSDN C0019572 Hairiness C1412747 Bbs2 gene HPO C0007398 Catatonic C0020787 Idaho HSDN C2919142 Short stature adverse event C0268390 Muckle-wells syndrome MalaCards|HPO C0234523 Apraxia, classic C0242422 Parkinsonian disorders HSDN C4084776 Weight loss C0020445 Hypercholesterolemia, familial HSDN C3887873 Hearing loss C0007621 Neoplastic cell transformation HSDN C3665347 Vision impaired C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C0270261 Edema newborn C0456071 Perinatal skin disorder nos UMLS C0018784 Deafness sensorineural C1568248 Usher syndrome, type iii OrphaNet|HPO|MalaCards C0151786 Weakness muscle C3665624 Serum calcium below normal HSDN C4085317 Diarrhea frequency C0027666 Neoplasms, radiation-induced HSDN C0042024 Urine incontinence C1962986 Glaucoma adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0221269 Pseudolymphoma HSDN C3665347 Vision impaired C3164344 Adult onset autosomal dominant leukodystrophy HPO C0030552 Paralysis partial C0039516 Tennis elbow HSDN C2984058 Have pain C0042850 Vitamin b deficiency HSDN C0037384 Snore C1963064 Anxiety adverse event HSDN C0151311 Cranial nerve palsy C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome MalaCards C0042963 Symptoms vomiting C0024636 Malocclusion HSDN C4084788 Have dizziness C0022738 Klippel-feil syndrome HSDN C0036572 Convulsion C1136249 Mental retardation, x-linked HSDN|HPO C1557397 Adverse event associated with pain C0038940 Surgical wound dehiscence HSDN C0000737 Abdomen pain C4086168 Childhood ovarian non-germinomatous germ cell tumor UMLS C0270948 Neurogenic muscular atrophy C1276035 Pena-shokeir syndrome type i MalaCards C3541349 Syncope C2930902 Bidirectional tachycardia MalaCards C0036572 Convulsion C0019195 Hepatitis, viral, human HSDN C0460137 Push down or depress C3888138 Monosomy x MalaCards C3815497 Cough C0037397 Behavior social HSDN C1963249 Tinnitus adverse event C0006325 Bruxism HSDN C0751460 Flaccid quadriplegia C0796028 Ataxia, fatal x-linked, with deafness and loss of vision MalaCards|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0006060 Boutonneuse fever HSDN C0497406 Over weight C2586211 Thrombosis of blood vessel HSDN C0042928 Paralysis vocal cord C0038454 Cerebrovascular accident HSDN C1069915 Vertigo C0024530 Malaria HSDN C0152227 Tearing excessive C1857144 Dyskeratosis congenita, autosomal recessive 1 MalaCards|HPO C0015402 Hemorrhage eye C0015503 Factor vii deficiency HSDN C1963281 Vomiting adverse event C0030305 Pancreatitis HSDN C0151686 Growth retardation C1839320 Childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness MalaCards C0518090 Frequency of pain question C0042384 Vasculitis HSDN C0031911 Pigment deposition C0278878 Adult glioblastoma MalaCards C1963252 Tremor adverse event C1853250 Spinocerebellar ataxia 23 HPO C3541349 Syncope C0003615 Appendicitis HSDN C2984057 Have nausea C2711591 Infection by anisakidae MalaCards C0020672 Body temperature decreased C0025521 Inborn errors of metabolism HSDN C4084766 Vomiting C0039730 Thalassemia HSDN C0004093 Asthenia C0027813 Neuritis HSDN C0151686 Growth retardation C0268680 Biotin deficiency MalaCards C0011206 Delirium acute C0040046 Thrombophlebitis HSDN C0162285 Edema eyelid C0751552 Malignant neoplasm of thymus MalaCards C3641756 Have diarrhea C1550639 Specimen type - fistula HSDN C1963093 Dizziness adverse event C0038019 Spondylosis HSDN C0149793 Transient monocular blindness C0022078 Iris diseases HSDN C2984057 Have nausea C0276786 Human balantidiasis MalaCards C0024902 Mastodynia C0020507 Hyperplasia HSDN C0878753 Unspecified lack of expected normal physiological development in childhood C0497409 Other nutritional; endocrine; and metabolic disorders UMLS C1963170 Hypothermia adverse event C0007873 Uterine cervical neoplasm HSDN C0034933 Abnormal reflexes C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C1963170 Hypothermia adverse event C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C3898969 Have been vomiting C0007193 Cardiomyopathy, dilated HSDN C4085548 Usual severity dizziness C0162526 Aids-related opportunistic infections HSDN C0023012 Delay language C1859570 Bardet-biedl syndrome 12 HPO C0020455 Hypergammaglobulinemia C0034069 Pulmonary fibrosis HSDN C1963180 Neck pain adverse event C0024081 Angina, ludwig HSDN C1963252 Tremor adverse event C0023473 Myeloid leukemia, chronic HSDN C4084769 Vomiting frequency C0175683 Citrullinemia HPO C2024893 Cardiovascular surgery result: fatigue C0035228 Respiratory hypersensitivity HSDN C1971624 Appetite absent C0235782 Gallbladder carcinoma OrphaNet C1963086 Confusion adverse event C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C1962972 Proteinuria adverse event C0023269 Leiomyosarcoma HSDN C3658248 Enlarged waist elevated triglycerides C0010054 Coronary arteriosclerosis HSDN C0026838 Spasticity muscle C1845892 Hprt deficiency, neurologic variant HPO C0010520 Skin cyanosis C0013069 Double outlet right ventricle HSDN C4085862 Bothered by nausea C0012979 Canine disease HSDN C0024031 Back pain lower back C1963198 Pancreatitis adverse event HSDN C4085210 Usual severity pain C0001422 Adenofibroma HSDN C3898969 Have been vomiting C0034065 Pulmonary embolism HSDN C0427055 Face weakness C1969106 Osteopetrosis, autosomal recessive 4 MalaCards|HPO C1579931 Depressed - symptom C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C0265279 Kniest dysplasia MalaCards|HPO C0030552 Paralysis partial C3536984 Vitamin d-resistant rickets, x-linked HSDN C1557397 Adverse event associated with pain C0032319 Pneumopericardium HSDN C0686770 Leser-trelat sign C1275160 Eruptive basal cell papillomata UMLS C3463815 Feel fatigue C0033873 Psychiatry HSDN C4084775 Usual severity weight loss C0024419 Waldenstrom macroglobulinemia HSDN C0028738 Nystagmus C0600268 Cheilitis granulomatosa MalaCards C4084802 Usual severity diarrhea C0398623 Thrombophilia HSDN C4085210 Usual severity pain C0150277 Meditations HSDN C4084725 Usual severity cough C1263846 Attention deficit hyperactivity disorder HSDN C0221166 Paraparesis C0020097 Htlv-i infections HSDN C2911647 Weight gain adverse event C0019112 Hemorrhoids HSDN C1145670 Failure respiratory C2931468 Cystic hamartomata of lung and kidney OrphaNet|MalaCards C0026838 Spasticity muscle C0003469 Anxiety disorders HSDN C0851578 Disorder sleep C0021933 Intussusception HSDN C1557397 Adverse event associated with pain C3714644 Thymus neoplasms HSDN C0042571 Vertigo subjective C0474820 Glomerocytoma tympanicum HSDN C0020305 Fetal edema C3469521 Fanconi anemia, complementation group a (disorder) HSDN C0424755 Fever symptoms C0032241 Pleuropneumonia HSDN C2032395 Pelvic pain on the left C1962979 Burn adverse event HSDN C0030486 Extremity paralysis, lower C0019553 Contracture hips HSDN C4084767 Bothered by vomiting C0596170 Binge eating disorder HSDN C0851578 Disorder sleep C0043145 Whiplash HSDN C4084767 Bothered by vomiting C0025500 Mesothelioma HSDN C4085862 Bothered by nausea C0037286 Skin neoplasms HSDN C0025287 Meningitis-like C0006118 Brain neoplasms HSDN C0020455 Hypergammaglobulinemia C0036421 Systemic scleroderma HSDN C4042891 Sleep wake disorders C0029882 Otitis media HSDN C0026884 Muteness C0007771 Intracranial arteriosclerosis HSDN C1961131 Cough adverse event C0011884 Diabetic retinopathy HSDN C0424755 Fever symptoms C0021364 Male infertility HSDN C0271215 Blindness legal C0004943 Behcet syndrome MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C1961835 Gaucher disease, type 1 MalaCards C4084767 Bothered by vomiting C0013926 Aeroembolism HSDN C0018681 Headache, cephalalgia C0024205 Lymphadenitis HSDN C0011991 Loose stools C0030330 Panniculitis, peritoneal HSDN C0027066 Myoclonic jerking C0162672 Merrf syndrome MalaCards|HPO C0497406 Over weight C0038160 Staphylococcal infections HSDN C0023014 Developmental disorder language C0002871 Anemia HSDN C0018772 Deafness C2186740 Reported urticaria HSDN C3539023 Pelvic pain increasing in frequency C0019693 Hiv infections HSDN C0015230 Exanthem C0037169 Sindbis fever UMLS C1961131 Cough adverse event C0041234 Chagas disease OrphaNet|MalaCards C0020305 Fetal edema C1291329 Transaldolase deficiency OrphaNet|HPO|MalaCards C0042798 Vision dim C0015300 Exophthalmos HSDN C2029884 Hearing loss by exam C0796202 Wittwer syndrome MalaCards C0349588 Stature short C1839729 Mental retardation, skeletal dysplasia, and abducens palsy MalaCards C4084776 Weight loss C0546837 Malignant neoplasm of esophagus OrphaNet|MalaCards C0027498 Nausea vomiting C1527226 Crst syndrome MalaCards C1963093 Dizziness adverse event C0024305 Lymphoma, non-hodgkin HSDN C1963170 Hypothermia adverse event C0024530 Malaria HSDN C0149793 Transient monocular blindness C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C3665492 Pigmentations C0339527 Leber congenital amaurosis MalaCards C0033774 Skin pruritus C0042373 Vascular diseases HSDN C2984058 Have pain C0041107 Trisomy HSDN C0042963 Symptoms vomiting C0017416 Genital neoplasms, female HSDN C0242936 Center pain C2004487 Vaginal spasm HSDN C0391860 Diffuse inflammations C0860257 Nongranulomatous ulcerative jejunoileitis UMLS C0476250 Head neck mass C0398684 Orofacial sarcoid UMLS C4085210 Usual severity pain C0013124 Behavior drinking HSDN C0349506 Sun sensitivity C0432254 Singleton merten syndrome HPO C4085210 Usual severity pain C0022364 Jaw neoplasms HSDN C0851578 Disorder sleep C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C3539890 Pelvic pain causes awakening at night C0227791 Discharge vaginal HSDN C0700078 Deep tendon reflex decrease C0751335 Scapuloperoneal form of spinal muscular atrophy MalaCards|HPO C0027796 Neuralgias C0019829 Hodgkin disease HSDN C0237326 Defecation pain C3281084 Congenital disorder of glycosylation, type ir MalaCards C0151786 Weakness muscle C0040046 Thrombophlebitis HSDN C0018681 Headache, cephalalgia C0027819 Neuroblastoma HSDN C0007859 Pain neck C0027663 Neoplasms, multiple primary HSDN C0015672 Decreased energy C0031350 Pharyngitis HSDN C0015672 Decreased energy C1552262 Nurse practitioner - family HSDN C0026821 Cramp C0013418 Abnormal labor HSDN C4085862 Bothered by nausea C0012147 Dientamoebiases DiseaseOntology C1882272 Pain adverse event by ctcae anatomic descriptor C0028064 Niemann-pick diseases HSDN C2237041 Shox gene with short stature C3150652 Fanconi renotubular syndrome 2 MalaCards|HPO C1850830 Exercise-induced muscle pain C3714933 Myopathy due to myoadenylate deaminase deficiency MalaCards C0020903 Illusion C4085311 Depression - recess HSDN C3641756 Have diarrhea C0032587 Polyradiculoneuropathy HSDN C2132198 Abnormal blistering of the skin C0406357 Skin peeling disorder OrphaNet C0948431 Partial conductive deafness C0018777 Conductive hearing loss UMLS C0019079 Bloody sputum C1336185 Stage iib adenocarcinoma of lung UMLS C3665347 Vision impaired C1274789 Ligneous conjunctivitis MalaCards C0015469 Facial paralysis C0034088 Pulmonary valve insufficiency HSDN C0015300 Ocular proptosis C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards|HPO C1963281 Vomiting adverse event C0013080 Down syndrome HSDN C0036572 Convulsion C0051981 Anti-leprosy vaccine HSDN C1527344 Dysphonia C0270726 Alexander disease OrphaNet|MalaCards C0518090 Frequency of pain question C0521170 Fracture due to osteoporosis HSDN C0013456 Pain ear C1384671 Mros gene HSDN C0015672 Decreased energy C1333043 Chronic myelomonocytic leukemia-1 UMLS C4085222 Nausea C1861848 Paragangliomas 4 MalaCards C0040822 D tremors C0037397 Behavior social HSDN C0018926 Emesis bloody C0012819 Diverticular disease of colon HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0022363 Jaw fracture HSDN C1279888 Proteinuria of undiagnosed cause C1860518 Vasculopathy, retinal, with cerebral leukodystrophy MalaCards|HPO C0427190 Ataxia, truncal C0394006 Dysequilibrium syndrome HPO|UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1509147 Histiocytoma HSDN C4084769 Vomiting frequency C1962963 Osteoporosis adverse event HSDN C0019079 Bloody sputum C0854970 Adenosquamous cell lung carcinoma recurrent UMLS C0020455 Hypergammaglobulinemia C0037278 Skin diseases, infectious HSDN C0011991 Loose stools C3489393 Hiatal hernia HSDN C0036572 Convulsion C2936779 Hydroxymethylbilane synthase deficiency MalaCards C3146279 Coma C0024198 Lyme disease HSDN C2984057 Have nausea C0032708 Disorders of porphyrin metabolism HSDN C0003469 Anxiety disorder C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0027497 Queasy C0000771 Abnormalities, drug induced HSDN C0019521 Hiccoughs C0032787 Postoperative complications HSDN C0007166 Cardiac output decreased C0018814 Heart rupture, post-infarction HSDN C4085211 Pain distress question C0036211 Sarcoma 180 HSDN C0242936 Center pain C1527348 Brain hypoxia HSDN C0036572 Convulsion C2749862 Mitochondrial neurogastrointestinal encephalopathy syndrome, rrm2b-related HPO C2984058 Have pain C0039786 Therapeutic communities HSDN C3815497 Cough C0520538 Tracheobronchopathia osteoplastica MalaCards C0231528 Muscle pain generalized C0020538 Hypertensive disease HSDN C1963249 Tinnitus adverse event C0751771 Sleep bruxism HSDN C0009676 Confusion state C0007766 Intracranial aneurysm HSDN C0857305 Thrombocytopenia purpura C0276275 Disease due to parvoviridae HSDN C3898969 Have been vomiting C4084909 Depression subordinate domain HSDN C1549543 Administration method - pain C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C0851578 Disorder sleep C0015579 Family characteristics HSDN C1963180 Neck pain adverse event C0032285 Pneumonia HSDN C0030486 Extremity paralysis, lower C0011875 Diabetic angiopathies HSDN C1963177 Muscle pain adverse event C0554636 Canicola fever MalaCards C3815497 Cough C0042075 Urologic diseases HSDN C3539895 Pelvic pain occurs with bowel movement C0563150 Catastrophization HSDN C0013404 Respiratory difficulty C0439840 Reflex motion descriptor HSDN C0036572 Convulsion C0270846 Epileptic drop attack UMLS C1557397 Adverse event associated with pain C0008523 Neoplasm choroid HSDN C1963090 Dehydration adverse event C2749175 Mineralocorticoid deficiency, isolated HPO C0032617 High urine output C0041327 Tuberculosis, pulmonary HSDN C1963281 Vomiting adverse event C0000809 Abortion, habitual HSDN C0242670 Chronic vegetative state C0014544 Epilepsy HSDN C3898969 Have been vomiting C0019202 Hepatolenticular degeneration HSDN C4084768 Usual severity vomiting C0040156 Thyrotoxicosis HSDN C3665492 Pigmentations C0349538 Anus; melanoma MalaCards C0028961 Urine output decreased C2909036 Twin twin transfusion HSDN C3827868 Tachycardia by ecg finding C0221055 Paramyotonia congenita (disorder) MalaCards C0005745 Blepharoptosis C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C0149793 Transient monocular blindness C0338437 Neurocysticercosis HSDN C0035229 Respiratory function impaired C2930798 Alexanders leukodystrophy MalaCards C0036572 Convulsion C0269660 Eclampsia added to pre-existing hypertension UMLS C0221232 Welts C0149526 Urticaria, allergic UMLS C0018772 Deafness C3494419 Deformities, dentofacial HSDN C4084727 Cough frequency C0003949 Asbestosis HSDN C0012833 Dizzy C0155515 Hyperactive labyrinth-unilat. UMLS C0042928 Paralysis vocal cord C2984289 Melanoma pathway HSDN C0027497 Queasy C0020517 Hypersensitivity HSDN C2220057 Fainting preceded C0340854 Situational syncope UMLS C0042928 Paralysis vocal cord C0036946 Sheep--diseases HSDN C1557397 Adverse event associated with pain C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0027498 Nausea vomiting C0007570 Celiac disease DiseaseOntology C0013404 Respiratory difficulty C0020502 Hyperparathyroidism HSDN C0018784 Deafness sensorineural C0023051 Laryngeal diseases HSDN C0036572 Convulsion C1844873 Charcot-marie-tooth disease, x-linked recessive, 2 (disorder) OrphaNet C0030552 Paralysis partial C0085433 Acquired joint deformities HSDN C4049602 Hyperactivity C2750246 Pitt hopkins like syndrome 1 HPO C0036572 Convulsion C0011644 Scleroderma MalaCards C4084767 Bothered by vomiting C0019699 Hiv seropositivity HSDN C0406146 Meningococcal rash C0025303 Meningococcal infections UMLS C2919142 Short stature adverse event C1327915 Congenital amegakaryocytic thrombocytopenia OrphaNet|HPO C4084788 Have dizziness C0027831 Neurofibromatosis 1 HSDN C2096293 Ent surgical result ear vertigo C0017638 Glioma HSDN C0518090 Frequency of pain question C0162790 Harassment sexual HSDN C0030200 Intractable pain C0037744 Perceptual spatial orientation HSDN C0221166 Paraparesis C1504464 Endoleak HSDN C0424755 Fever symptoms C0019097 Hemorrhagic fever, argentinian MalaCards C4084723 Constipation C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C2096293 Ent surgical result ear vertigo C0019360 Herpes zoster disease HSDN C4084723 Constipation C0009475 Community mental health service HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042568 Vertebrobasilar insufficiency HSDN C0036659 Sensation disorder C0000833 Abscess HSDN C4084727 Cough frequency C0276119 Q-fever pneumonia MalaCards C4084726 Distress cough C0008677 Bronchitis, chronic MalaCards C2106658 Complaint of seasonal allergic reaction C0018621 Hay fever UMLS C0028738 Nystagmus C1850386 Giant axonal neuropathy 1 HPO C1579931 Depressed - symptom C0002875 Cooley's anemia OrphaNet|HPO C0349489 Fetal hypoxia C0033975 Psychotic disorders HSDN C4085317 Diarrhea frequency C0037928 Spinal cord diseases HSDN C0040822 D tremors C0026363 Mohr-claussen syndrome MalaCards C0007758 Cerebellar ataxia C0020102 Htlv-ii infections HSDN C0234132 Pyramidal sign C1843807 Basal ganglia disease, biotin-responsive MalaCards|UMLS C1384666 Decreased hearing C3275508 Multiple congenital anomalies-hypotonia-seizures syndrome 2 MalaCards C0151686 Growth retardation C2931524 Seemanova-lesny syndrome OrphaNet C0851578 Disorder sleep C0018817 Atrial septal defects HSDN C0035078 Failure kidney C0015625 Fanconi anemia MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0022373 Disease, jejunal HSDN C0023530 Leukopenia C2675860 Diamond-blackfan anemia 4 MalaCards C0015672 Decreased energy C0033375 Prolactinoma OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0079744 Diffuse large b-cell lymphoma HSDN C0015672 Decreased energy C2931518 Plexosarcoma MalaCards C0231807 Dyspnea exertional C2749560 Methemoglobinemia, type ii HPO C2984058 Have pain C0011989 Camurati-engelmann syndrome HSDN C0004134 Dyssynergia C0033922 Psychomotor disorders MalaCards C0036572 Convulsion C3278384 Hypoinsulinemic hypoglycemia with hemihypertrophy MalaCards C4085210 Usual severity pain C2073625 X-ray of chest: pleural effusion HSDN C1263846 Attention deficit disorder with hyperactivity C1848488 Pierre robin syndrome with fetal chondrodysplasia OrphaNet|HPO C0040264 Ear ringing sound C0017601 Glaucomas HSDN C3898969 Have been vomiting C0042134 Uterine hemorrhage HSDN C0151686 Growth retardation C0024748 Alpha-mannosidosis HPO C0004604 Pain back C0018799 Heart diseases HSDN C0028738 Nystagmus C2936741 Syndrome xxyy MalaCards C0424755 Fever symptoms C0221056 Adult type dermatomyositis MalaCards C3898969 Have been vomiting C0002514 Amino acid metabolism, inborn errors HSDN C0848203 Male pelvic pain C0025202 Melanoma HSDN C0424755 Fever symptoms C0010414 Infection by cryptococcus neoformans HSDN C4085642 Level of joint stiffness C2931548 Krasnow qazi yermakov syndrome OrphaNet|MalaCards C4084802 Usual severity diarrhea C0023448 Lymphoid leukemia HSDN C0085631 Abnormal excitement C1956346 Coronary artery disease HSDN C0542476 Forgetful C0038868 Progressive supranuclear palsy OrphaNet|HPO|UMLS C0085688 Engorgement breast C0405322 Breast engorgement in pregnancy, the puerperium or lactation with antenatal complication UMLS C0020458 Hyperhydrosis C3539003 Neuropathy, hereditary sensory and autonomic, type vi MalaCards C1557397 Adverse event associated with pain C0041313 Hepatic tuberculosis HSDN C0036572 Convulsion C0009324 Ulcerative colitis HSDN C0917816 Deficiency mental C0795878 Monosomy 22 MalaCards C1963071 Back pain adverse event C0037199 Sinusitis HSDN C0004604 Pain back C1090821 Sepsis (invertebrate) HSDN C0033774 Skin pruritus C0040136 Thyroid neoplasm HSDN C1963091 Diarrhea adverse event C0152156 Dystocia HSDN C0020672 Body temperature decreased C0151516 Thyroid hypoplasia HPO C0036572 Convulsion C1835905 Epilepsy, nocturnal frontal lobe, type 4 HPO C3641756 Have diarrhea C0027868 Neuromuscular diseases HSDN C0043094 Weight gain C0007193 Cardiomyopathy, dilated HSDN C0028738 Nystagmus C1858677 Leber congenital amaurosis 3 (disorder) MalaCards|HPO C0015672 Decreased energy C0151516 Thyroid hypoplasia OrphaNet|HPO C1557397 Adverse event associated with pain C0040124 Thyroglossal duct cyst HSDN C0020538 Hbp C1859564 Bardet-biedl syndrome 3 HPO C3541349 Syncope C0340629 Aortic aneurysm without mention of rupture nos HSDN C0232466 Feeding difficulty C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C3539020 Pelvic pain decreasing in frequency C0037051 Behavior illness HSDN C4085211 Pain distress question C0008412 Choline deficiency HSDN C0007758 Cerebellar ataxia C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C0036659 Sensation disorder C0007820 Cerebrovascular disorders HSDN C0030193 Sense of pain C0391976 Pain disorder UMLS C0040822 D tremors C1268935 Congenital thrombotic thrombocytopenic purpura HPO|UMLS C2029884 Hearing loss by exam C2609414 Acute kidney injury HSDN C0271215 Blindness legal C0457133 Muscle eye brain disease MalaCards C0037317 Sleep disturbance C0751362 Narcolepsy-cataplexy syndrome OrphaNet|MalaCards C4085661 Usual severity nausea C0242383 Age related macular degeneration HSDN C0015672 Decreased energy C1443900 Inhalational botulism OrphaNet|MalaCards C2911645 Weight loss adverse event C0684274 Self regulation HSDN C3641756 Have diarrhea C0085092 Parenting behavior HSDN C0917816 Deficiency mental C1863557 Young simpson syndrome HPO C3662844 Nocturia associated with benign prostatic hypertrophy C0028734 Nocturia UMLS C4084775 Usual severity weight loss C0024301 Lymphoma, follicular OrphaNet|HSDN|HPO|MalaCards C0030552 Paralysis partial C0022661 Kidney failure, chronic HSDN C3539891 Pelvic pain to the rear C0796561 Melanoma vaccines HSDN C0019572 Hairiness C0006160 Brenner tumor HSDN C3539890 Pelvic pain causes awakening at night C1299262 Sarcoma - category (morphologic abnormality) HSDN C4084766 Vomiting C1963068 Atrial flutter adverse event HSDN C0013404 Respiratory difficulty C0085278 Antiphospholipid syndrome HSDN C0428977 Pulse rate decrease C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards|HPO C0242936 Center pain C0034895 Rectovaginal fistula HSDN C1557397 Adverse event associated with pain C1962974 Chylothorax adverse event HSDN C0009421 Comatose C0031212 Personality disorders HSDN C2024893 Cardiovascular surgery result: fatigue C0302148 Blood clot HSDN C4084726 Distress cough C0041316 Lymph node tuberculosis DiseaseOntology|MalaCards C2919142 Short stature adverse event C2677682 Rett syndrome, zappella variant HPO C0023530 Leukopenia C3266027 Autoimmune polyendocrine syndrome type 3 MalaCards C0518090 Frequency of pain question C0014901 Aesthetic HSDN C0151889 Reflexes tendon increased C0796066 Microcephaly-cervical spine fusion anomalies OrphaNet|MalaCards C0700078 Deep tendon reflex decrease C1845359 Spinal muscular atrophy, distal, x-linked 3 MalaCards|HPO C4084723 Constipation C0431406 Asymmetric crying face association OrphaNet|HPO C4084802 Usual severity diarrhea C0020625 Hyponatremia HSDN C0036572 Convulsion C0033586 Failure, prosthesis HSDN C0033774 Skin pruritus C1335968 Vulvar intraepithelial neoplasia, differentiated type UMLS C0035078 Failure kidney C2347126 Microscopic polyarteritis MalaCards C0013362 Dysarthrias C1858680 Familial encephalopathy with neuroserpin inclusion bodies MalaCards|HPO C3887873 Hearing loss C0025284 Meningeal neoplasms HSDN C0010200 Cough symptom C1336082 Thymic squamous cell carcinoma UMLS C0002962 Angina C0020476 Hyperlipoproteinemias HSDN C0000737 Abdomen pain C0035228 Respiratory hypersensitivity HSDN C0034150 Skin purpura C0026636 Mouth diseases HSDN C4084773 Bothered by weight gain C0004623 Bacterial infections HSDN C4085548 Usual severity dizziness C0029877 Ear inflammation HSDN C0042963 Symptoms vomiting C1332251 Ampulla of vater squamous cell carcinoma UMLS C0011991 Loose stools C0023443 Hairy cell leukemia HSDN C1549543 Administration method - pain C0702166 Acne HSDN C0413252 Hypothermia due to exposure C0010709 Cyst HSDN C1557397 Adverse event associated with pain C0016124 Finger injury HSDN C4084725 Usual severity cough C0034531 Experimental radiation injuries HSDN C0026838 Spasticity muscle C0242188 Spider bites HSDN C4049644 Depression C0751435 Hyperphenylalaninaemia MalaCards C1000483 Genus anemia C0432313 Epidermolysis bullosa simplex with hypodontia MalaCards C0008031 Pain chest C0153414 Malignant neoplasm of middle third of esophagus MalaCards C4085549 Dizziness C0000771 Abnormalities, drug induced HSDN C4084725 Usual severity cough C0012546 Diphtheria HSDN C0008031 Pain chest C1706728 Adrenal gland composite pheochromocytoma UMLS C0003811 Cardiac rhythm disturbance C1856186 Deafness enamel hypoplasia nail defects MalaCards C3641756 Have diarrhea C0949272 Iieocolitis MalaCards C0149793 Transient monocular blindness C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C3815497 Cough C0038187 Starvation HSDN C2919142 Short stature adverse event C2931811 Chromosome 18, trisomy 18p MalaCards C3539023 Pelvic pain increasing in frequency C0004275 Attitude health HSDN C0030193 Sense of pain C0026718 Mucormycosis HSDN C3539022 Pelvic pain decreasing in severity C2911643 Encounter due to family history of osteoporosis HSDN C0028738 Nystagmus C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy HPO C0020458 Hyperhydrosis C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C0023014 Developmental disorder language C0032787 Postoperative complications HSDN C0000737 Abdomen pain C0006109 Brain damage, chronic HSDN C1963091 Diarrhea adverse event C0024899 Mastocytosis OrphaNet|MalaCards C0878638 Tongue signs C2931750 Cleft lip-palate with characteristic facies, intestinal malrotation, and lethal congenital heart disease MalaCards C0851578 Disorder sleep C0305062 Tetanus toxoids HSDN C3641755 Have constipation C0003864 Arthritis HSDN C0007758 Cerebellar ataxia C0997768 Glaucoma HSDN C3539896 Pelvic pain occurs with urination C0012979 Canine disease HSDN C0427068 Legs weakness C2931276 Spastic paraplegia 17 HPO C0003467 Angst C0266526 Norrie disease OrphaNet|HPO|MalaCards C0027796 Neuralgias C1546533 Specimen source codes - abscess HSDN C1279888 Proteinuria of undiagnosed cause C0035229 Respiratory insufficiency HSDN C0518090 Frequency of pain question C0037198 Sinus thrombosis, intracranial HSDN C4084784 Diarrhea C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C0917816 Deficiency mental C1866174 Phosphoglycerate dehydrogenase deficiency MalaCards|HPO C3163620 Hypotension adverse event C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C1962972 Proteinuria adverse event C3146297 Study of behavior during childhood HSDN C0007398 Catatonic C0030297 Pancreatic neoplasm HSDN C0036572 Convulsion C0175683 Citrullinemia HSDN|HPO|UMLS C1549543 Administration method - pain C0037023 Sialadenitis HSDN C4042891 Sleep wake disorders C0017185 Gastrointestinal neoplasms HSDN C1279888 Proteinuria of undiagnosed cause C0001969 Alcoholic intoxication HSDN C0018777 Deafness, conductive C0016549 Foreign body reaction HSDN C1963086 Confusion adverse event C0752332 Lupus vasculitis, central nervous system HSDN C0020649 Blood pressure decreased C2919861 Medullary cystic kidney disease type 1 MalaCards C0015672 Decreased energy C0032463 Polycythemia vera OrphaNet|HPO C0036572 Convulsion C0220669 Familial benign neonatal epilepsy OrphaNet|UMLS|HPO|MalaCards C0026838 Spasticity muscle C1847501 Glut1 deficiency syndrome OrphaNet|UMLS|MalaCards C4085211 Pain distress question C0024638 Class ii division 2 malocclusion HSDN C0427068 Legs weakness C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C0018772 Deafness C0041954 Ureteral diseases and syndromes HSDN C0232466 Feeding difficulty C0268250 Gaucher disease, type 2 (disorder) MalaCards|HPO C0009806 Constipate C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0036572 Convulsion C3715128 Hypocalcemia, autosomal dominant 1 UMLS C3898969 Have been vomiting C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C0424755 Fever symptoms C0347555 Friction blister HSDN C0152020 Atony stomach C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards C4084784 Diarrhea C1834211 Ganglioneuromatosis of the alimentary tract HPO C3146279 Coma C0026528 Moral code HSDN C1963164 Lymphopenia adverse event C1860168 Achondroplasia, so-called, and severe combined immunodeficiency OrphaNet|MalaCards C0018784 Deafness sensorineural C3887877 Deficiency of glycerate kinase MalaCards C3898969 Have been vomiting C0220710 Medium-chain acyl-coenzyme a dehydrogenase deficiency HPO C1384666 Decreased hearing C0029294 Orofaciodigital syndromes MalaCards|HSDN C0234146 Absent reflex C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C0042023 Urination frequency C0398791 Nijmegen breakage syndrome OrphaNet|HPO|MalaCards C0027066 Myoclonic jerking C0007761 Myoclonic cerebellar dyssynergia UMLS C2024893 Cardiovascular surgery result: fatigue C1552527 Clinic / center - developmental disabilities HSDN C0026838 Spasticity muscle C0005940 Bone diseases HSDN C0030193 Sense of pain C1709663 Pioscc UMLS C4084724 Usual severity constipation C0014836 Escherichia coli infections HSDN C0042024 Urine incontinence C0036161 Sandhoff disease HPO C0020672 Body temperature decreased C0039841 Thiamine deficiency HSDN C2315100 Pediatric failure to thrive C1859534 Bare lymphocyte syndrome, type ii, complementation group a HPO C4085211 Pain distress question C0003892 Neurogenic arthropathy HSDN C1963077 Bone pain adverse event C0524988 Schnitzler syndrome OrphaNet|MalaCards C0030193 Sense of pain C0021141 Inappropriate adh syndrome HSDN C0024031 Back pain lower back C0452160 Lumbago; sciatica UMLS C1963071 Back pain adverse event C0019196 Hepatitis c HSDN C0022107 Fussiness C0020497 Cortical congenital hyperostosis DiseaseOntology|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0008775 Ciguatera poisoning HSDN C0018991 Paralysis one side of body C0043097 Perception, weight HSDN C1549543 Administration method - pain C0035235 Respiratory syncytial virus infections HSDN C4084775 Usual severity weight loss C0031046 Pericarditis HSDN C0013395 Indigestion C1527298 Dysentery, bacillary HSDN C0009676 Confusion state C2239176 Liver carcinoma HSDN C0150055 Pain chronic C1956346 Coronary artery disease HSDN C3641756 Have diarrhea C0398689 Hyper-igm immunodeficiency syndrome, type 1 HPO C3815497 Cough C0085183 Neoplasms, second primary HSDN C4084773 Bothered by weight gain C0011303 Demyelinating diseases HSDN C2024893 Cardiovascular surgery result: fatigue C3814778 Hemolytic index HSDN C4084727 Cough frequency C1565106 Headache disorders, primary HSDN C0151786 Weakness muscle C0086543 Cataract nos HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023798 Lipoma HSDN C1557397 Adverse event associated with pain C0037305 Neoplasm, skull HSDN C0231218 Malaise generalized C2981637 Stage iva hilar cholangiocarcinoma UMLS C3463815 Feel fatigue C0751552 Malignant neoplasm of thymus MalaCards C3665492 Pigmentations C1836841 Ceroid lipofuscinosis, neuronal, 9 (disorder) MalaCards C1557397 Adverse event associated with pain C0005974 Bone resorption HSDN C0030552 Paralysis partial C0017926 Glycogen storage disease type vii OrphaNet|HPO|MalaCards C4084773 Bothered by weight gain C0035229 Respiratory insufficiency HSDN C0235153 Sensory hallucination C3888102 Frontotemporal dementia with motor neuron disease MalaCards C0020673 Hypothermia (central) (local) C0009375 Colonic neoplasms HSDN C0234378 Postural tremor C1853445 Parkinson disease 7, autosomal recessive early-onset MalaCards|HPO|UMLS C3887638 Failure to thrive in infant C1853736 Congenital disorder of glycosylation, type iib OrphaNet|HPO|MalaCards C3146279 Coma C0085437 Meningitis, bacterial HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001486 Adenovirus infections HSDN C2096293 Ent surgical result ear vertigo C0009450 Disease caused by microorganism HSDN C0427055 Face weakness C1843225 Charcot-marie-tooth disease, axonal, type 2e (disorder) HPO C0344428 Ventricular tachycardia by ecg finding C2677491 Cardiomyopathy, familial hypertrophic, 12 HPO C0018772 Deafness C0023521 Globoid cell leukodystrophy OrphaNet|HPO|MalaCards C0011991 Loose stools C0034089 Pulmonary valve stenosis HSDN C0020796 Profoundly mentally retarded C2752007 Congenital disorder of glycosylation, type io MalaCards C4084773 Bothered by weight gain C0010674 Cystic fibrosis HSDN C4085317 Diarrhea frequency C1136033 Cutaneous mastocytosis MalaCards C0600142 Flash hot C2030274 Heavy bleeding between periods HSDN C0009024 Clonus C1843569 Spastic paraplegia 24, autosomal recessive (disorder) MalaCards|UMLS C0002170 Alopecia disorders C0263428 Burnett schwartz berberian syndrome MalaCards C1963137 Hydrocephalus adverse event C1848600 Vater association with hydrocephalus HPO C0020673 Hypothermia (central) (local) C0038525 Subarachnoid hemorrhage HSDN C0587048 Upper extremity mass C1290130 Melanocytic naevus of upper limb UMLS C0042571 Vertigo subjective C0042133 Uterine fibroids HSDN C0242936 Center pain C0023787 Lipodystrophy HSDN C4084774 Have weight loss C0007762 Cerebellar neoplasms HSDN C1963154 Renal failure adverse event C1848561 Methylmalonic acidemia with homocystinuria MalaCards C4085222 Nausea C0039730 Thalassemia HSDN C4085317 Diarrhea frequency C0162627 Skin diseases, bacterial HSDN C4084897 Sleep disturbance subordinate domain C0268365 Marfanoid hypermobility syndrome MalaCards C0427055 Face weakness C4082296 Facial nerve paresis UMLS C0242936 Center pain C0040559 Toxoplasmosis in animals HSDN C0041834 Erythematous condition C0392436 Pemphigus, benign MalaCards C4025720 Pseudobulbar behavioral symptoms C1859807 Amyotrophic lateral sclerosis 2, juvenile (disorder) MalaCards|HPO C0349506 Sun sensitivity C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C0042755 Virilisation C0334695 Endometrial stromal tumors HSDN C0013428 Painful urination C1334281 Infiltrating bladder urothelial carcinoma UMLS C0007758 Cerebellar ataxia C0085388 Intracranial tuberculoma HSDN C0039870 Leanness C0236969 Substance-related disorders HSDN C0042963 Symptoms vomiting C1550639 Specimen type - fistula HSDN C1963063 Anorexia adverse event C0221036 Acrodermatitis enteropathica HPO C0576456 Poor feeding C1832390 Van maldergem wetzburger verloes syndrome MalaCards C0234428 Consciousness disturbance C3542499 Aminoacylase 2 deficiency OrphaNet|MalaCards C0086439 Activity decreased C0020538 Hypertensive disease HSDN C0009806 Constipate C0040034 Thrombocytopenia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004692 Balantidiasis MalaCards C1549543 Administration method - pain C0085315 Toxoplasmosis, cerebral HSDN C3539895 Pelvic pain occurs with bowel movement C2936403 46, xx disorders of sex development HSDN C0349506 Sun sensitivity C0032897 Prader-willi syndrome MalaCards|HPO C0010520 Skin cyanosis C0034050 Pulmonary alveolar proteinosis HSDN C1963184 Nystagmus adverse event C1855008 Mitochondrial complex ii deficiency MalaCards|HPO C4085317 Diarrhea frequency C0002986 Fabry disease MalaCards|HPO C0029163 Hemorrhage mouth C0007971 Cheilitis HSDN C0002624 Amnesia retrograde C0546983 Post-concussion syndrome HSDN C0009676 Confusion state C0233629 Thinking and speaking disturbances HSDN C0557874 Global developmental delay C3554657 Lissencephaly 5 MalaCards C3539020 Pelvic pain decreasing in frequency C0206630 Endometrial stromal sarcoma HSDN C0015672 Decreased energy C0432328 Xeroderma pigmentosum, variant form MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0035358 Retroperitoneal neoplasm HSDN C0033774 Skin pruritus C0001197 Acrodermatitis HSDN C3541349 Syncope C0035828 Romano-ward syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0010276 Craniopharyngioma HSDN C3641756 Have diarrhea C0040558 Toxoplasmosis HSDN C0018772 Deafness C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) MalaCards C0239376 Lower extremity pain C0749242 Systolic murmur new onset UMLS C0011991 Loose stools C0021603 Sleep initiation and maintenance disorders HSDN C0497406 Over weight C0005283 Beta thalassemia HSDN C0036572 Convulsion C0035228 Respiratory hypersensitivity HSDN C4084723 Constipation C0003507 Aortic valve stenosis HSDN C1963281 Vomiting adverse event C0031212 Personality disorders HSDN C0007758 Cerebellar ataxia C1968561 Xeroderma pigmentosum, type g-cockayne syndrome HPO C0018681 Headache, cephalalgia C0221021 Microangiopathic hemolytic anemia MalaCards C0027066 Myoclonic jerking C1263846 Attention deficit hyperactivity disorder HSDN C0000737 Abdomen pain C0018920 Hemangioma, cavernous HSDN C2203646 Jaundice C1704421 Skin pigmentation disorder HSDN C0030193 Sense of pain C0037974 Spirochaetales infections HSDN C0016382 Cutaneous vascular engorgement C0014859 Esophageal neoplasms HSDN C1384666 Decreased hearing C0040034 Thrombocytopenia HSDN C2203646 Jaundice C0033975 Psychotic disorders HSDN C0240859 Rales, basilar C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C0413252 Hypothermia due to exposure C0038661 Suicide HSDN C0242670 Chronic vegetative state C0018674 Head trauma HSDN C3887873 Hearing loss C0022658 Kidney diseases HSDN C0557874 Global developmental delay C0751161 Udpglucose 4-epimerase deficiency disease OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C1963119 Stomach ulcer adverse event HSDN C0012833 Dizzy C0019163 Hepatitis b HSDN C4085317 Diarrhea frequency C0027932 Neurotic disorders HSDN C1963252 Tremor adverse event C0178842 Sensory feedback HSDN C0242936 Center pain C0043019 Lateral medullary syndrome HSDN C4084768 Usual severity vomiting C0039128 Syphilis HSDN C0010200 Cough symptom C0003486 Aortic aneurysm HSDN C0042928 Paralysis vocal cord C0015397 Disorder of eye HSDN C0043094 Weight gain C0020651 Hypotension, orthostatic HSDN C0007758 Cerebellar ataxia C0009363 Congenital ocular coloboma (disorder) HSDN C0040264 Ear ringing sound C0038538 Effusion subdural HSDN C4085317 Diarrhea frequency C0585442 Osteosarcoma of bone HSDN C0042928 Paralysis vocal cord C0007121 Bronchogenic carcinoma HSDN C1557397 Adverse event associated with pain C1963266 Uveitis adverse event HSDN C1963091 Diarrhea adverse event C0518449 Control of hip fracture risk HSDN C0028738 Nystagmus C1704421 Skin pigmentation disorder MalaCards C4084773 Bothered by weight gain C1636667 Disorder characterized by eosinophilia HSDN C0015672 Decreased energy C0085257 Yin deficiency HSDN C4085222 Nausea C0041466 Typhoid fever HSDN C0034933 Abnormal reflexes C0010267 Cranial nerve neoplasms HSDN C1963071 Back pain adverse event C0001314 Acute disease HSDN C0042963 Symptoms vomiting C0007762 Cerebellar neoplasms HSDN C1963064 Anxiety adverse event C0342859 Harderoporphyria HPO C4050613 Anxiety C0751435 Hyperphenylalaninaemia MalaCards C0020458 Hyperhydrosis C3714948 Pachyonychia congenita 3 MalaCards C0023015 Language handicap C1621958 Glioblastoma multiforme MalaCards C0039070 Collapse fleeting C0011168 Deglutition disorders UMLS C0013132 Drooling C1859807 Amyotrophic lateral sclerosis 2, juvenile (disorder) MalaCards|HPO C0521161 Vasculitic eruption C0302295 Eruptions UMLS C0018784 Deafness sensorineural C1837640 Deafness, autosomal dominant 28 MalaCards|HPO C1384666 Decreased hearing C3542499 Aminoacylase 2 deficiency OrphaNet|MalaCards C0042024 Urine incontinence C0403555 Ochoa syndrome OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0032319 Pneumopericardium HSDN C1557397 Adverse event associated with pain C0019554 Dislocate hip HSDN C1090821 Sepsis C0079218 Fibromatosis, aggressive MalaCards|HPO C4084723 Constipation C0162820 Dermatitis, allergic contact HSDN C0022346 Yellow skin C0856761 Budd-chiari syndrome MalaCards|HPO C0018784 Deafness sensorineural C3151230 Deafness, autosomal recessive 61 MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0008925 Cleft palate HSDN C4085210 Usual severity pain C0022116 Ischemia HSDN C0850758 Pain pelvic C0014179 Endometritis HSDN C0155344 Spasm of conjugated gaze C0015397 Disorder of eye UMLS C4084723 Constipation C1848519 Waardenburg syndrome, type 4a OrphaNet|HPO|MalaCards C0426579 Anorexia symptom C0009450 Disease caused by microorganism HSDN C4084773 Bothered by weight gain C0014175 Endometriosis HSDN C0020458 Hyperhydrosis C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C3203358 Alveolar hypoventilation C0751941 Glossopharyngeal nerve disease or syndrome HSDN C3641756 Have diarrhea C1319688 Blister dose form HSDN C2984058 Have pain C0019348 Herpes simplex infections HSDN C2242996 Tingling C0043019 Lateral medullary syndrome HSDN C0036659 Sensation disorder C0017601 Glaucomas HSDN C0349588 Stature short C0265303 Acrocephalopolysyndactyly type iv MalaCards C1963177 Muscle pain adverse event C2931689 Dystrophia myotonica 2 MalaCards C0241210 Speaking delay C1839736 Wilson-turner x-linked mental retardation syndrome HPO C0042963 Symptoms vomiting C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C2106654 History of allergic reaction C0851444 Allergic conditions UMLS C3887638 Failure to thrive in infant C0016952 Galactosemias MalaCards|HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1963119 Stomach ulcer adverse event HSDN C0151686 Growth retardation C2751651 Chromosome 19q13.11 deletion syndrome OrphaNet C0002170 Alopecia disorders C2931059 Marie unna congenital hypotrichosis OrphaNet|HPO|MalaCards C1579931 Depressed - symptom C1527168 Bonnevie-ullrich syndrome MalaCards C0013404 Respiratory difficulty C0009373 Colonic diseases HSDN C0034933 Abnormal reflexes C0011570 Mental depression HSDN C0235031 Neurological complaint C0028738 Nystagmus UMLS C3641756 Have diarrhea C3553270 Diarrhea 6 MalaCards C0027066 Myoclonic jerking C1414216 Dystonia 6, torsion (disorder) MalaCards|HPO C1963252 Tremor adverse event C0699828 Serotonergic syndrome HSDN C0019209 Large liver C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C0030193 Sense of pain C0043251 Wounds and injuries HSDN C0007758 Cerebellar ataxia C2240374 Eosinophil count raised HSDN C4085862 Bothered by nausea C0878544 Cardiomyopathies HSDN C4085317 Diarrhea frequency C0162703 Pain sensitivity HSDN C4084774 Have weight loss C0023903 Liver neoplasms MalaCards C0522224 Palsied C0600041 Infective cystitis HSDN C0030193 Sense of pain C0040425 Tonsillitis HSDN C0010200 Cough symptom C0012691 Dislocations HSDN C2984058 Have pain C0702166 Acne HSDN C2984058 Have pain C0035801 Diseases rodent HSDN C1963249 Tinnitus adverse event C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0018772 Deafness C0029294 Orofaciodigital syndromes MalaCards|HSDN C1963281 Vomiting adverse event C0034067 Pulmonary emphysema HSDN C0027497 Queasy C0032131 Plasmacytoma HSDN C0009421 Comatose C0032787 Postoperative complications HSDN C0015300 Ocular proptosis C0796117 Pitt syndrome MalaCards C1963170 Hypothermia adverse event C0027746 Nerve degeneration HSDN C4084784 Diarrhea C0007867 Cervix diseases HSDN C4084788 Have dizziness C0030286 Pancreatic diseases HSDN C0027066 Myoclonic jerking C4050613 Anxiety scale (basc-2) HSDN C2029884 Hearing loss by exam C0546952 Congenital facial asymmetry HSDN C0022107 Fussiness C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0019209 Large liver C1306856 Megaloblastic anemia due to inborn errors of metabolism MalaCards C0011991 Loose stools C0026785 Munchhausen syndrome HSDN C2911645 Weight loss adverse event C0020443 Hypercholesterolemia HSDN C0344315 Mood depressed C0271097 Usher syndrome MalaCards C0028961 Urine output decreased C0021295 Infant, premature, diseases HSDN C0237326 Defecation pain C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C3641756 Have diarrhea C0026919 Mycobacterium infections, nontuberculous HSDN C2700617 Irritation - emotion C2936917 Infantile polyarteritis MalaCards C2237041 Shox gene with short stature C0013338 Pituitary dwarfism OrphaNet|MalaCards C0522224 Palsied C0030421 Paraganglioma HSDN C3665347 Vision impaired C1859069 Brittle bone disorder OrphaNet C4085222 Nausea C2586211 Thrombosis of blood vessel HSDN C0042963 Symptoms vomiting C3280378 Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia UMLS C3274924 Have been coughing C0017160 Gastroenteritis HSDN C0344428 Ventricular tachycardia by ecg finding C1857777 Arrhythmogenic right ventricular dysplasia, familial, 10 HPO C0013604 Edematous C0947622 Cholecystolithiasis HSDN C0004134 Dyssynergia C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0030193 Sense of pain C0018818 Ventricular septal defects HSDN C0151786 Weakness muscle C0035354 Axon reaction HSDN C1963067 Atrial fibrillation adverse event C4015368 Aortic aneurysm, familial thoracic 9 MalaCards C1971624 Appetite absent C0040436 Dental erosion HSDN C4084776 Weight loss C0042769 Virus diseases HSDN C0015672 Decreased energy C0037933 Spinal diseases HSDN C3274924 Have been coughing C0038356 Stomach neoplasms HSDN C0150055 Pain chronic C1963138 Hypertension adverse event HSDN C0027497 Queasy C0014849 Esophageal and gastric varices HSDN C1963071 Back pain adverse event C0031511 Pheochromocytoma HSDN C0221166 Paraparesis C0085136 Central nervous system neoplasms HSDN C0022346 Yellow skin C0010308 Congenital hypothyroidism HSDN C0812426 Kidney problem C0748315 Renal failure chronic progressive UMLS C0023380 Lethargy C0038874 Supratentorial neoplasms HSDN C0030975 Disorders perception C0003646 Aptitude HSDN C1963066 Joint pain adverse event C0085293 Hepatitis e MalaCards C0851578 Disorder sleep C0037928 Spinal cord diseases HSDN C0030794 Pelvis pain C1000483 Genus anemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018194 Giant cell granuloma HSDN C3665347 Vision impaired C0265240 Goldenhar syndrome MalaCards C0009024 Clonus C1850395 Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive HPO|UMLS C2024878 Cardiovascular surgery result: dyspnea C0024214 Lymphangiectasis HSDN C0028738 Nystagmus C0795832 9p tetrasomy MalaCards C4084773 Bothered by weight gain C0030500 Animal parasitic disease HSDN C0000737 Abdomen pain C0027666 Neoplasms, radiation-induced HSDN C0013404 Respiratory difficulty C0017168 Gastroesophageal reflux disease HSDN C2984058 Have pain C0024894 Mastitis HSDN C0005779 Clotting C0349499 Fetal cytomegalovirus syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0027794 Neural tube defects HSDN C3641756 Have diarrhea C0025309 Meningoencephalitis HSDN C3463815 Feel fatigue C0013990 Pathological accumulation of air in tissues HSDN C4084773 Bothered by weight gain C0018621 Hay fever HSDN C4085317 Diarrhea frequency C0750394 Wbc low HSDN C1260880 Nasal drip C1334920 Adenocarcinoma of nasal cavity UMLS C0013595 Eczematous dermatitis C2936739 Hyper-immunoglobulin e syndrome, autosomal dominant OrphaNet|HPO C2984058 Have pain C2936350 Plaque, atherosclerotic HSDN C0009806 Constipate C0005967 Bone neoplasms HSDN C4085211 Pain distress question C0002949 Aneurysm, dissecting HSDN C4085210 Usual severity pain C0021295 Infant, premature, diseases HSDN C1963086 Confusion adverse event C0021361 Female infertility HSDN C0041657 Consciousness loss C0009426 Combat disorders HSDN C4084775 Usual severity weight loss C3887532 Ulceration HSDN C2700617 Irritation - emotion C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C1963184 Nystagmus adverse event C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C4085210 Usual severity pain C0033839 Pseudorabies HSDN C4085210 Usual severity pain C0013575 Ectodermal dysplasia HSDN C0011991 Loose stools C2937287 Hematolysis HSDN C1963086 Confusion adverse event C0033903 Psychologic technic HSDN C1384666 Decreased hearing C3830518 Diabetic embryopathy MalaCards C0684343 Pseudophakia C0037286 Skin neoplasms HSDN C0018681 Headache, cephalalgia C0393745 Chronic post-traumatic headache UMLS C0005745 Blepharoptosis C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C1963184 Nystagmus adverse event C0035921 Congenital rubella syndrome OrphaNet|MalaCards C4084788 Have dizziness C0026780 Mumps HSDN C4084769 Vomiting frequency C0795623 Hepatitis a vaccine, inactivated HSDN C1549543 Administration method - pain C0010606 Adenoid cystic carcinoma HSDN C0003862 Pain joint C0021890 Intraoperative complications HSDN C4049644 Depression C0268250 Gaucher disease, type 2 (disorder) MalaCards C0547030 Sensory perceptual alteration: visual C0028850 Ocular motility disorders UMLS C0036572 Convulsion C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0019825 Voice hoarseness C0751336 Distal muscular dystrophies HSDN C0151786 Weakness muscle C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C0030193 Sense of pain C0036240 Response, satiety HSDN C0042571 Vertigo subjective C1263846 Attention deficit hyperactivity disorder HSDN C4084726 Distress cough C1527407 Eosinophilic pneumonia DiseaseOntology C0037384 Snore C3495422 Finding relating to sexuality and sexual activity HSDN C1963281 Vomiting adverse event C0019069 Hemophilia a HSDN C4084773 Bothered by weight gain C0027686 Pathologic neovascularization HSDN C0040034 Thrombocytopenia C0024530 Malaria OrphaNet|MalaCards C3274924 Have been coughing C0026650 Movement disorders HSDN C4085210 Usual severity pain C2827407 Infectious otitis media HSDN C4085862 Bothered by nausea C0007125 Carcinoma, ehrlich tumor HSDN C0151798 Liver necrosis C0854795 Resectable hepatic malignant neoplasm MalaCards C0042024 Urine incontinence C0015802 Femur fracture HSDN C0003862 Pain joint C0043346 Xeroderma pigmentosum OrphaNet|HPO|MalaCards C0036572 Convulsion C0006840 Candidiasis HSDN C0243026 Generalized infection C1851124 Desmoid disease, hereditary MalaCards C3203358 Alveolar hypoventilation C0860549 Refeed syndrome HSDN C4084775 Usual severity weight loss C0598402 Animal migration HSDN C3887638 Failure to thrive in infant C0242387 Mandibulofacial dysostosis MalaCards|HPO C0557874 Global developmental delay C1865134 Spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation OrphaNet|MalaCards C3665346 Loss sight C2751780 Retinitis pigmentosa, juvenile, spata7-related HPO C0040264 Ear ringing sound C0022116 Ischemia HSDN C1279888 Proteinuria of undiagnosed cause C0268146 Glucose-6-phosphate transport defect MalaCards|HPO C3641756 Have diarrhea C0038395 Streptococcal infections HSDN C1557397 Adverse event associated with pain C0039240 Supraventricular tachycardia HSDN C4085661 Usual severity nausea C0027051 Myocardial infarction HSDN C0027497 Queasy C0597916 Heuristic HSDN C0085636 Light sensitivity C0035012 Reiter syndrome MalaCards C0004134 Dyssynergia C2677590 Congenital disorder of glycosylation, type in MalaCards|HPO|UMLS C0011991 Loose stools C0560694 Bottles per feed HSDN C0013395 Indigestion C0018188 Granuloma HSDN C0017181 Gastrointestinal bleed C0023092 Lassa fever MalaCards C0034155 Thrombotic thrombocytopenic purpura C0017662 Glomerulonephritis, membranoproliferative HSDN C0009398 Color vision defects C0155305 Optic neuropathy, ischemic HSDN C3898969 Have been vomiting C0018805 Heart injuries HSDN C0242936 Center pain C0013291 Duodenal neoplasms HSDN C1962972 Proteinuria adverse event C1856143 Hemolytic uremic syndrome, typical MalaCards C0042571 Vertigo subjective C0004623 Bacterial infections HSDN C3898969 Have been vomiting C0023676 Life style HSDN C0013604 Edematous C0023467 Leukemia, myelocytic, acute HSDN C1557397 Adverse event associated with pain C0022366 Jaw, edentulous HSDN C1971624 Appetite absent C1005359 Pica pica bird HSDN C3541349 Syncope C0026127 Military psychiatry HSDN C4084802 Usual severity diarrhea C0268151 Classical galactosemia MalaCards|HPO C0013395 Indigestion C0040053 Thrombosis HSDN C0424755 Fever symptoms C0029124 Optic atrophy HSDN C0851578 Disorder sleep C3542413 Cdisc adas-cog - comprehension HSDN C0009421 Comatose C1720777 Functional laterality HSDN C1963091 Diarrhea adverse event C2219717 Menstrual periods stopped for over 6 months HSDN C2911645 Weight loss adverse event C0024301 Lymphoma, follicular OrphaNet|HSDN|HPO|MalaCards C0017565 Gingiva hemorrhage C0017205 Gaucher disease MalaCards C0009460 Communication impairment C2981150 Uranostaphyloschisis HSDN C2984057 Have nausea C0018944 Hematoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0742343 Acute chest syndrome HSDN C0009080 Finger clubbing C1333764 Gastric cronkhite canada polyposis MalaCards C0398650 Idiopathic thrombocytopenia purpura C0079027 Blood loss, surgical HSDN C0015672 Decreased energy C0013808 Electroconvulsive therapy HSDN C1962972 Proteinuria adverse event C0003873 Rheumatoid arthritis HSDN C3887638 Failure to thrive in infant C0175694 Smith-lemli-opitz syndrome MalaCards|HSDN|HPO C1963091 Diarrhea adverse event C0031762 Photosensitivity disorders HSDN C0917816 Deficiency mental C0795865 Chromosome 17, trisomy 17p OrphaNet|MalaCards C0009806 Constipate C0011175 Dehydration UMLS C0030486 Extremity paralysis, lower C0162678 Neurofibromatoses HSDN C2032396 Pelvic pain on the right C0409354 Flexion contracture of hip HSDN C0020639 Hypoproteinaemia C0175692 Johanson-blizzard syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C0010314 Cri-du-chat syndrome OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C2350521 Gustatory perception HSDN C3665386 Abnormal vision C1869114 Weill-marchesani syndrome, autosomal recessive MalaCards C3887873 Hearing loss C0042830 Perception visual HSDN C0030193 Sense of pain C0269051 Acute endomyometritis UMLS C1963091 Diarrhea adverse event C0038459 Equine strongyle infection HSDN C4084776 Weight loss C0038186 Reflex, startle HSDN C0041834 Erythematous condition C1970712 Multiple endocrine neoplasia, type iv MalaCards|HPO C1557397 Adverse event associated with pain C0041234 Chagas disease HSDN C0013378 Dysgensia C0017409 Herpes zoster oticus HSDN C2219924 Feeling persecuted, expecting trickery C0747249 Paranoid ideation UMLS C1384666 Decreased hearing C1865366 Deafness, autosomal dominant 15 MalaCards|HPO C4084726 Distress cough C1963083 Cholecystitis adverse event HSDN C0015230 Exanthem C0023518 Leukocytosis UMLS C0042571 Vertigo subjective C2984572 Malaria pathway HSDN C4085549 Dizziness C1735340 Multifocal ventricular extrasystoles MalaCards C0023012 Delay language C2750082 Deafness, autosomal recessive 79 MalaCards|HPO C0019825 Voice hoarseness C1414216 Dystonia 6, torsion (disorder) MalaCards C1963184 Nystagmus adverse event C3279775 Multiple congenital anomalies-hypotonia-seizures syndrome 1 MalaCards C4084788 Have dizziness C0677866 Brain stem neoplasms HSDN C0241137 Skin pallor C0027822 Neurodermatitis HSDN C0015672 Decreased energy C0023676 Life style HSDN C1963274 Vasculitis adverse event C0040021 Thromboangiitis obliterans OrphaNet|MalaCards C1527344 Dysphonia C0085653 Pyogenic granuloma HSDN C0005745 Blepharoptosis C0026691 Mucocutaneous lymph node syndrome MalaCards C1963087 Constipation adverse event C3887532 Ulceration HSDN C4084774 Have weight loss C0011875 Diabetic angiopathies HSDN C0018834 Brash C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C0242936 Center pain C0015401 Foreign body in eye HSDN C1963091 Diarrhea adverse event C0018809 Heart neoplasm HSDN C0007859 Pain neck C0010068 Coronary heart disease HSDN C4084726 Distress cough C3714509 Nutrition disorders HSDN C0033774 Skin pruritus C0013100 Dracontiasis OrphaNet|MalaCards C0085631 Abnormal excitement C0022387 Jervell-lange nielsen syndrome HSDN C0151311 Cranial nerve palsy C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0240444 Nail thickening C3280501 Inflammatory skin and bowel disease, neonatal, 1 MalaCards|UMLS C0020580 Decreased sensation C0004935 Animal ethology HSDN C3887638 Failure to thrive in infant C3151444 Dyskeratosis congenita, autosomal recessive, 4 MalaCards C0018772 Deafness C0002874 Aplastic anemia HSDN C1961131 Cough adverse event C2004491 Cicatrix HSDN C0231835 Respiration rate increased C1857355 Leigh syndrome , french canadian type HPO C4084727 Cough frequency C0021368 Inflammation HSDN C4084725 Usual severity cough C0238378 Desquamative interstitial pneumonia MalaCards C2362324 Pediatric obesity C0010276 Craniopharyngioma HSDN C0004134 Dyssynergia C0030318 Panic state HSDN C0398650 Idiopathic thrombocytopenia purpura C0014859 Esophageal neoplasms HSDN C1963063 Anorexia adverse event C0085682 Hypophosphatemia HSDN C0522224 Palsied C0038454 Cerebrovascular accident HSDN C2029884 Hearing loss by exam C1963064 Anxiety adverse event HSDN C0027497 Queasy C0015397 Disorder of eye HSDN C2096293 Ent surgical result ear vertigo C0151467 Addisonian crisis MalaCards C4084766 Vomiting C0023521 Globoid cell leukodystrophy MalaCards|HPO C0162298 Stiffness joints C0265260 Chondrodysplasia, grebe type OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0268080 Hypercalcemia, idiopathic, of infancy HPO C4084769 Vomiting frequency C0028432 Nose diseases HSDN C3815497 Cough C0036341 Schizophrenia HSDN C0231528 Muscle pain generalized C2931826 Potassium aggravated myotonia OrphaNet|HPO|UMLS C1384666 Decreased hearing C0752180 Bacterial cns infection HSDN C0033774 Skin pruritus C1335303 Pancreatic foamy gland adenocarcinoma UMLS C1963091 Diarrhea adverse event C0014852 Esophageal diseases HSDN C2984058 Have pain C0024810 Marijuana smoking HSDN C3463815 Feel fatigue C0343068 Familial cold urticaria OrphaNet|HPO|MalaCards C0013421 Dystonia C0004935 Animal ethology HSDN C3641755 Have constipation C0032371 Poliomyelitis HSDN C0237326 Defecation pain C2931294 Wiedemann grosse dibbern syndrome MalaCards C1962972 Proteinuria adverse event C0018213 Graves disease HSDN C0018965 Blood urine C1421354 Umps gene HPO C4084724 Usual severity constipation C1000483 Genus anemia HSDN C0030486 Extremity paralysis, lower C0027902 Neuropsychological diagnosis HSDN C2984058 Have pain C0302280 Adrenogenital syndrome HSDN C4085661 Usual severity nausea C0085111 Ankle injury HSDN C0581358 Gastric spasm C0026848 Myopathy UMLS C3887638 Failure to thrive in infant C1856306 Gsd iv, neuromuscular form, adult, with isolated myopathy HPO C2096293 Ent surgical result ear vertigo C0006145 Breast diseases HSDN C1963281 Vomiting adverse event C1962958 Hematoma adverse event HSDN C0036572 Convulsion C0022283 Incontinentia pigmenti achromians OrphaNet|UMLS|HPO|MalaCards C4085862 Bothered by nausea C0013990 Pathological accumulation of air in tissues HSDN C4085317 Diarrhea frequency C0029401 Osteitis deformans HSDN C0424755 Fever symptoms C0018798 Congenital heart defects HSDN C0042024 Urine incontinence C0038395 Streptococcal infections HSDN C0042963 Symptoms vomiting C0376547 Aromatherapy HSDN C0851578 Disorder sleep C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0030552 Paralysis partial C2911643 Encounter due to family history of osteoporosis HSDN C4084774 Have weight loss C2117118 X-ray of toe: deformity contracture HSDN C0002962 Angina C0085129 Bronchial hyperreactivity HSDN C4084802 Usual severity diarrhea C0085258 Deficiency, yang HSDN C0018772 Deafness C3542499 Aminoacylase 2 deficiency OrphaNet|MalaCards C0518090 Frequency of pain question C0012746 Dissociative disorder HSDN C0019825 Voice hoarseness C1721007 Pachyonychia congenita, type 2 (disorder) HPO|UMLS C0745966 Lower leg edema C4039900 Venous stasis ulcer co-occurrent with edema of lower leg UMLS C0497247 Blood pressure elevation C0431716 Nephronophthisis - medullary cystic disease MalaCards C2362324 Pediatric obesity C0149887 Slipped capital femoral epiphyses HSDN C0151786 Weakness muscle C2931482 Neurofibromatosis-noonan syndrome MalaCards|HPO C3815497 Cough C0887976 Chlamydophila infections HSDN C0028738 Nystagmus C1855995 L-2-hydroxyglutaric aciduria MalaCards|HPO C0231341 Aging premature C0339527 Leber congenital amaurosis HSDN C0917816 Deficiency mental C2931058 Marfan syndrome type 2 MalaCards C0020673 Hypothermia (central) (local) C0919267 Ovarian neoplasm HSDN C0015970 Fever unknown origin C0013182 Drug allergy HSDN C0020673 Hypothermia (central) (local) C0018802 Congestive heart failure HSDN C2242996 Tingling C0206734 Hemangioblastoma HSDN C4084802 Usual severity diarrhea C0017150 Gastrinoma OrphaNet|MalaCards C0030193 Sense of pain C1656583 Rosacea HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001314 Acute disease HSDN C0013421 Dystonia C0206255 Malaria vaccine HSDN C1963071 Back pain adverse event C0006413 Burkitt lymphoma HSDN C1279888 Proteinuria of undiagnosed cause C0010481 Cushing syndrome HSDN C3274924 Have been coughing C0007282 Carotid stenosis HSDN C0040822 D tremors C0036868 Sex chromosome aberrations HSDN C0750426 Wbc elevated C2930812 Generalized elastolysis MalaCards C1961131 Cough adverse event C1956391 Temporal arteritis MalaCards|HPO C0026858 Musculoskeletal pain C0036231 Sarcocystosis HSDN C4084774 Have weight loss C0017416 Genital neoplasms, female HSDN C0234132 Pyramidal sign C4225393 3-methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia UMLS C0349489 Fetal hypoxia C0037369 Smoking HSDN C2242996 Tingling C0014511 Epithelial cyst HSDN C0003862 Pain joint C0012979 Canine disease HSDN C4085661 Usual severity nausea C0428977 Bradycardia HSDN C0042963 Symptoms vomiting C0079744 Diffuse large b-cell lymphoma HSDN C4085210 Usual severity pain C1963059 Adrenal insufficiency adverse event HSDN C4085210 Usual severity pain C0037942 Spinal osteophytosis HSDN C2919142 Short stature adverse event C0432262 Dysosteosclerosis OrphaNet|HPO|MalaCards C4084784 Diarrhea C0036093 Salivary gland diseases HSDN C2984057 Have nausea C0152164 Cyclical vomiting syndrome (disorder) MalaCards C1279888 Proteinuria of undiagnosed cause C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C0020505 Excessive eating C1881674 Medical device emits smoke HSDN C0151827 Pain eye C0015414 Eye neoplasms HSDN C0243026 Generalized infection C2700553 Omenn syndrome MalaCards|HPO C0033377 Caudal displacement C0432336 Cutis laxa, recessive, type i OrphaNet|HPO C0016199 Pain flank C3272295 Renal cell carcinoma associated with neuroblastoma UMLS C0027066 Myoclonic jerking C1090821 Sepsis (invertebrate) HSDN C4085642 Level of joint stiffness C1837073 Spondylometaphyseal dysplasia with cone-rod dystrophy HPO C0004604 Pain back C0010054 Coronary arteriosclerosis HSDN C0023530 Leukopenia C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C0013404 Respiratory difficulty C0599412 Lordosis [mating posture] HSDN C0040259 Tinea pedis C0036262 Sarcoptic itch HSDN C0018681 Headache, cephalalgia C1548777 Specimen reject reason - hemolysis HSDN C0042963 Symptoms vomiting C0426616 Vomiting blood - fresh UMLS C2242996 Tingling C0268328 Porphobilinogen synthase deficiency MalaCards|HPO C0004604 Pain back C0497327 Dementia HSDN C0151786 Weakness muscle C1856059 Mthfr deficiency, thermolabile type HPO C0428977 Pulse rate decrease C3553374 Coenzyme q10 deficiency, primary, 5 MalaCards C0020672 Body temperature decreased C0020522 Delayed hypersensitivity HSDN C0015970 Fever unknown origin C0428953 Ecg infarction myocardial HSDN C2029884 Hearing loss by exam C0032371 Poliomyelitis HSDN C1963184 Nystagmus adverse event C1864872 Spondyloepimetaphyseal dysplasia, genevieve type MalaCards|HPO C0037317 Sleep disturbance C1847501 Glut1 deficiency syndrome MalaCards|UMLS C4084775 Usual severity weight loss C0004031 Aspergillosis, allergic bronchopulmonary OrphaNet|MalaCards C0018991 Paralysis one side of body C1000483 Genus anemia HSDN C4085862 Bothered by nausea C1881674 Medical device emits smoke HSDN C1549543 Administration method - pain C0040028 Thrombocythemia, essential HSDN C0235153 Sensory hallucination C0796022 Lujan fryns syndrome HPO C0019079 Bloody sputum C0002736 Amyotrophic lateral sclerosis HSDN C0033377 Caudal displacement C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C3641755 Have constipation C1546847 Entity name part type - family HSDN C0005745 Blepharoptosis C4012727 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 MalaCards C0003811 Cardiac rhythm disturbance C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C4084726 Distress cough C0004623 Bacterial infections HSDN C0727671 Red cross toothache drops C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084775 Usual severity weight loss C0029295 Oropharyngeal neoplasms HSDN C4084768 Usual severity vomiting C0002871 Anemia HSDN C0424755 Fever symptoms C0038358 Gastric ulcer HSDN C0040822 D tremors C0043251 Wounds and injuries HSDN C1961131 Cough adverse event C1565489 Renal insufficiency HSDN C0037763 Spasm C0001418 Adenocarcinoma HSDN C4084784 Diarrhea C0030793 Pelvis tumor HSDN C4084784 Diarrhea C0027813 Neuritis HSDN C0035078 Failure kidney C0403529 Anti-glomerular basement membrane disease MalaCards C0242936 Center pain C0751895 Vasospasm, intracranial HSDN C3898969 Have been vomiting C0042781 Visceral myopathy MalaCards C3146279 Coma C0035613 Rift valley fever MalaCards C3887873 Hearing loss C1510455 Acrocephalosyndactylia MalaCards|HSDN C0019209 Large liver C0268425 Alstrom syndrome MalaCards|HPO C0009676 Confusion state C0027051 Myocardial infarction HSDN C2984058 Have pain C0019911 Hookworm infections HSDN C4084788 Have dizziness C0376527 Neoplasm, skull base HSDN C1856661 Cornea cloudy C0086651 Mucopolysaccharidosis, mps-iv-a HPO C0011206 Delirium acute C0014068 Encephalomalacia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0080032 Pleural effusion, malignant HSDN C0005745 Blepharoptosis C0085261 Proteus syndrome HPO C0151686 Growth retardation C0043208 Wolman disease OrphaNet|HPO C4085661 Usual severity nausea C0023343 Leprosy HSDN C3641756 Have diarrhea C0007095 Carcinoid tumor HSDN C1963065 Apnea adverse event C0004933 Behavior modification technique HSDN C4085211 Pain distress question C0014356 Enterocolitis HSDN C0000737 Abdomen pain C1306503 Congenital exomphalos HSDN C0557874 Global developmental delay C0795942 Fitzsimmons-guilbert syndrome HPO C0030193 Sense of pain C1335355 Adenoid cystic carcinoma of parotid UMLS C0030975 Disorders perception C0007097 Carcinomas HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C2751830 Long qt syndrome 12 MalaCards|HPO C0009676 Confusion state C0000768 Congenital abnormality HSDN C0033774 Skin pruritus C0024636 Malocclusion HSDN C0030193 Sense of pain C0022079 Iris neoplasms HSDN C0424755 Fever symptoms C3146297 Study of behavior during childhood HSDN C0018681 Headache, cephalalgia C0007771 Intracranial arteriosclerosis HSDN C4084767 Bothered by vomiting C0947622 Cholecystolithiasis HSDN C0020580 Decreased sensation C0333157 Colloid cysts HSDN C3887784 Decreased urine output C0020192 Hyaline membrane disease HSDN C1963281 Vomiting adverse event C0014121 Bacterial endocarditis HSDN C3641755 Have constipation C1838569 Caudal dysgenesis syndrome HPO C0003811 Cardiac rhythm disturbance C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal OrphaNet|HPO C0040822 D tremors C3813607 Infantile gastroesophageal reflux HSDN C4084776 Weight loss C0036467 Scrofula MalaCards C4085661 Usual severity nausea C0017536 Giardiasis DiseaseOntology|HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0030486 Extremity paralysis, lower C0003962 Ascites HSDN C0232466 Feeding difficulty C0079683 Herlitz disease OrphaNet|HPO|MalaCards C0031911 Pigment deposition C2713442 Polyposis, adenomatous intestinal MalaCards C0030200 Intractable pain C0029443 Osteomyelitis HSDN C0003862 Pain joint C0003507 Aortic valve stenosis HSDN C0151786 Weakness muscle C0796274 Brown-vialetto-van laere syndrome OrphaNet C0004604 Pain back C0016977 Gall bladder diseases HSDN C0518090 Frequency of pain question C0042847 Vitamin b 12 deficiency HSDN C0086565 Liver function abnormal C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0020672 Body temperature decreased C0007789 Cerebral palsy HSDN C4085211 Pain distress question C0024419 Waldenstrom macroglobulinemia HSDN C0010520 Skin cyanosis C0040580 Tracheal diseases HSDN C0848203 Male pelvic pain C0042029 Urinary tract infection HSDN C0023012 Delay language C1845243 Mental retardation, x-linked, syndromic, claes-jensen type OrphaNet|HPO|MalaCards C0344315 Mood depressed C0017205 Gaucher disease OrphaNet|MalaCards C4085210 Usual severity pain C0848558 Hypospadias HSDN C0002962 Angina C0850803 Anaphylaxis (non medication) HSDN C0043094 Weight gain C0001175 Acquired immunodeficiency syndrome HSDN C0018926 Emesis bloody C1552262 Nurse practitioner - family HSDN C0000737 Abdomen pain C0032285 Pneumonia HSDN|UMLS C2911647 Weight gain adverse event C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084774 Have weight loss C0030297 Pancreatic neoplasm MalaCards|HSDN C4084725 Usual severity cough C0178282 Hernia of abdominal cavity HSDN C0151786 Weakness muscle C0751870 Heredodegenerative disorders, nervous system HSDN C0015672 Decreased energy C0000833 Abscess HSDN C1549543 Administration method - pain C1963139 Hypopigmentation adverse event HSDN C0042024 Urine incontinence C0005586 Bipolar disorder HSDN C0242936 Center pain C0948089 Acute coronary syndrome HSDN C1000483 Genus anemia C0023788 Whipple disease MalaCards C3178766 Nociceptive pain C0012644 Animal disease models HSDN C0040264 Ear ringing sound C0151740 Intracranial hypertension HSDN C1963167 Memory impairment adverse event C0917890 Pineocytoma OrphaNet|MalaCards C3829611 Nausea frequency C0016483 Food preferences HSDN C3463815 Feel fatigue C0018021 Goiter HSDN C2237041 Shox gene with short stature C2931811 Chromosome 18, trisomy 18p MalaCards C0022107 Fussiness C3501891 Mitochondrial dna depletion myopathy, autosomal recessive MalaCards C0026838 Spasticity muscle C1263846 Attention deficit hyperactivity disorder MalaCards|HSDN C4084775 Usual severity weight loss C0013386 Dyskinesia, drug-induced HSDN C1963071 Back pain adverse event C0003469 Anxiety disorders HSDN C1963091 Diarrhea adverse event C1306794 Wound botulism MalaCards C0018681 Headache, cephalalgia C3897121 Recurrent childhood protoplasmic astrocytoma UMLS C0426579 Anorexia symptom C0860603 Anxiety symptoms HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0015409 Eye injuries penetrating HSDN C3541349 Syncope C0004275 Attitude health HSDN C1963086 Confusion adverse event C0023524 Leukoencephalopathy, progressive multifocal HSDN C3539891 Pelvic pain to the rear C0006118 Brain neoplasms HSDN C0032227 Effusion pleural C2931241 Primary intestinal lymphangiectasis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0029422 Osteochondrodysplasias HSDN C4085211 Pain distress question C0033785 Pseudarthrosis HSDN C0270948 Neurogenic muscular atrophy C1863924 Megalanecephaly polymicrogyria-polydactyly hydrocephalus syndrome MalaCards|HPO C0007166 Cardiac output decreased C0042512 Ventricular outflow obstruction HSDN C3714552 Strength decreased C0023518 Leukocytosis UMLS C0015469 Facial paralysis C0041582 Ulcer HSDN C1142068 Arcus lipoides C0344532 Congenital anterior embryotoxon UMLS C0018775 Hearing loss bilateral C0029124 Optic atrophy HSDN C0232466 Feeding difficulty C0852654 21-hydroxylase deficiency MalaCards C0013421 Dystonia C0008626 Congenital chromosomal disease HSDN C0037771 Paraparesis spastic C0751871 Autoimmune diseases of the nervous system HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1956418 Torsion abnormality HSDN C0013604 Edematous C0343101 Wells syndrome OrphaNet|MalaCards C0600142 Flash hot C0043251 Wounds and injuries HSDN C0518090 Frequency of pain question C1414542 Fbn1 gene HSDN C0424755 Fever symptoms C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0349489 Fetal hypoxia C1552527 Clinic / center - developmental disabilities HSDN C0010520 Skin cyanosis C0042485 Venous insufficiency HSDN C0026826 High muscle tone C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0751295 Memory loss or impairment C2931082 Familial apoceruloplasmin deficiency MalaCards C1963087 Constipation adverse event C2609414 Acute kidney injury HSDN C0024282 Lymphocytosis C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0007758 Cerebellar ataxia C0004935 Animal ethology HSDN C0004093 Asthenia C1000483 Genus anemia HSDN C0042025 Urinary incontinence stress C0041948 Uremia HSDN C0013604 Edematous C0007772 Intracranial arteriovenous malformation HSDN C0026838 Spasticity muscle C0037036 Sialorrhea HSDN C0033774 Skin pruritus C0020981 Angioimmunoblastic lymphadenopathy HSDN C4084802 Usual severity diarrhea C0221204 Lytic lesion HSDN C3539023 Pelvic pain increasing in frequency C0004935 Animal ethology HSDN C0018524 Hallucinate C0041466 Typhoid fever HSDN C1963087 Constipation adverse event C3244301 Coverage level - family HSDN C1384666 Decreased hearing C3280402 Sclerosteosis 2 MalaCards C2911647 Weight gain adverse event C0015674 Chronic fatigue syndrome HSDN C4084802 Usual severity diarrhea C1522133 High cholesterol level HSDN C1000483 Genus anemia C2931838 Familial hdl deficiency MalaCards C0024031 Back pain lower back C0023364 Leptospirosis HSDN C4084784 Diarrhea C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0042024 Urine incontinence C0017181 Gastrointestinal hemorrhage HSDN C0009806 Constipate C4225203 Hypotonia, infantile, with psychomotor retardation and characteristic facies 2 UMLS C3665347 Vision impaired C1867451 Pseudoxanthoma elasticum, heterozygous HPO C1962972 Proteinuria adverse event C0038354 Stomach diseases HSDN C0040822 D tremors C3554605 Mc3dn2 MalaCards|UMLS C1963184 Nystagmus adverse event C1959626 Mevalonic aciduria MalaCards|HPO C0413252 Hypothermia due to exposure C1762616 Meningioma, benign, no icd-o subtype HSDN C4084897 Sleep disturbance subordinate domain C3151069 Chromosome 17p13.1 deletion syndrome MalaCards C4084774 Have weight loss C0001624 Adrenal gland neoplasms HSDN C1557397 Adverse event associated with pain C0041341 Tuberous sclerosis HSDN C0018772 Deafness C2931669 Chromosome 8, mosaic trisomy MalaCards C2029884 Hearing loss by exam C0597109 Nurse's role HSDN C2024893 Cardiovascular surgery result: fatigue C2028283 History of premature birth HSDN C0522224 Palsied C0008065 Childhood behavior HSDN C0030552 Paralysis partial C0398689 Hyper-igm immunodeficiency syndrome, type 1 HSDN C0020578 Hyperventilate C0008370 Cholestasis HSDN C4084897 Sleep disturbance subordinate domain C1855772 Absent corpus callosum cataract immunodeficiency MalaCards|HPO C1549543 Administration method - pain C0005591 Avian disease HSDN C1963281 Vomiting adverse event C0035066 Renal artery obstruction HSDN C0024031 Back pain lower back C0039336 Gustatory sense HSDN C0033774 Skin pruritus C4085311 Depression - recess HSDN C1000483 Genus anemia C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C0522224 Palsied C0018946 Hematoma, subdural HSDN C0917816 Deficiency mental C1968748 Gangliosidosis, generalized gm1, type i, with cardiac involvement HPO C0036572 Convulsion C0019880 Homocystinuria HSDN C0242936 Center pain C0014065 Congenital cerebral hernia HSDN C4085317 Diarrhea frequency C4014516 Diarrhea 7 MalaCards C0027066 Myoclonic jerking C0016658 Fracture bone HSDN C3641756 Have diarrhea C0002453 Amenorrhea HSDN C0009806 Constipate C0014836 Escherichia coli infections HSDN C0020615 Hypoglycemia nos C2931660 Autosomal recessive fructose 1, 6-diphosphatase deficiency MalaCards C0086439 Activity decreased C3149705 Parkinson disease 1, autosomal dominant lewy body HPO C1963249 Tinnitus adverse event C0016658 Fracture bone HSDN C1963249 Tinnitus adverse event C0265321 Wyburn-mason syndrome MalaCards C0013604 Edematous C0007621 Neoplastic cell transformation HSDN C1557397 Adverse event associated with pain C0013712 Ego HSDN C0023012 Delay language C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C4084726 Distress cough C0018674 Head trauma HSDN C0000737 Abdomen pain C1258104 Diffuse scleroderma HSDN C2911645 Weight loss adverse event C0036323 Schistosomiasis HSDN C0263629 Tumor-like lesions of the skin C0263642 Skin vegetations, nos UMLS C0013421 Dystonia C0018944 Hematoma HSDN C0018520 Breath odor C0038454 Cerebrovascular accident HSDN C0042963 Symptoms vomiting C0018944 Hematoma HSDN C0178417 Anhedonia C2713543 Biofeedback eeg HSDN C0042024 Urine incontinence C3888013 Hypnoses HSDN C4084775 Usual severity weight loss C0024198 Lyme disease HSDN C0042963 Symptoms vomiting C0011581 Depressive disorder HSDN C3641755 Have constipation C1855923 Hyperphosphatasia with mental retardation MalaCards|HPO C2937287 Hematolysis C0002895 Anemia, sickle cell MalaCards C4049644 Depression C0038868 Progressive supranuclear palsy OrphaNet C2024893 Cardiovascular surgery result: fatigue C0003490 Aortic arch syndrome MalaCards C0497247 Blood pressure elevation C0268335 Ehlers-danlos syndrome type 1 MalaCards|HPO C0043068 Friderichsen-waterhouse syndrome C0008049 Chicken pox HSDN C4085210 Usual severity pain C0027149 Myxoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0973461 Dysphasia C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked OrphaNet|HPO C4084769 Vomiting frequency C0011875 Diabetic angiopathies HSDN C0036572 Convulsion C2676759 Thrombophilia due to protein c deficiency, autosomal recessive MalaCards|HPO|UMLS C1963071 Back pain adverse event C0021361 Female infertility HSDN C4084725 Usual severity cough C0702221 Tactual discrimination HSDN C0022346 Yellow skin C0279661 Acinar cell carcinoma of pancreas UMLS C0018681 Headache, cephalalgia C1275668 Melanotic medulloblastoma UMLS C4084784 Diarrhea C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0013604 Edematous C0043124 West nile fever HSDN C2024893 Cardiovascular surgery result: fatigue C0717360 Disease lyme vaccine HSDN C0000786 Abortion spontaneous C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0030297 Pancreatic neoplasm HSDN C0018681 Headache, cephalalgia C0021368 Inflammation HSDN C0019214 Hepatosplenomegaly C0153458 Pancreas head cancer malignant MalaCards C4085211 Pain distress question C0024138 Lupus erythematosus, discoid HSDN C1557397 Adverse event associated with pain C0042582 Vesicovaginal fistula HSDN C3641756 Have diarrhea C0032320 Peritoneal free air HSDN C0030193 Sense of pain C0015409 Eye injuries penetrating HSDN C1549543 Administration method - pain C0030424 Paragonimiasis HSDN C1963071 Back pain adverse event C0019348 Herpes simplex infections HSDN C0242936 Center pain C0006413 Burkitt lymphoma HSDN C0242936 Center pain C0002957 Anger HSDN C0026826 High muscle tone C0024814 Marinesco-sjogren syndrome MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C3495559 Juvenile arthritis HSDN C1557397 Adverse event associated with pain C0017570 Gingival neoplasms HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0037274 Dermatologic disorders HSDN C0009806 Constipate C0242350 Erectile dysfunction HSDN C4084776 Weight loss C0030297 Pancreatic neoplasm MalaCards|HSDN C4084726 Distress cough C0009404 Colorectal neoplasms HSDN C0018772 Deafness C0005591 Avian disease HSDN C2911645 Weight loss adverse event C0017150 Gastrinoma OrphaNet|MalaCards C0151686 Growth retardation C0242343 Panhypopituitarism OrphaNet C4085862 Bothered by nausea C1962963 Osteoporosis adverse event HSDN C0009806 Constipate C0278544 Stage ii rectal cancer UMLS C0349588 Stature short C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0232857 Psychogenic dysuria C0810265 Other and unspecified mental conditions UMLS C3641755 Have constipation C0023467 Leukemia, myelocytic, acute HSDN C0018784 Deafness sensorineural C1962958 Hematoma adverse event HSDN C0344428 Ventricular tachycardia by ecg finding C3150754 Glycogen storage disease xv MalaCards C0035232 Diaphragmatic paralysis C0007137 Squamous cell carcinoma HSDN C0520966 Coordination impaired C1865981 Friedreich ataxia 2 MalaCards C0851578 Disorder sleep C1962986 Glaucoma adverse event HSDN C0020578 Hyperventilate C0268680 Biotin deficiency MalaCards C4084784 Diarrhea C2350019 Solitary pulmonary nodule HSDN C4085317 Diarrhea frequency C0018916 Hemangioma HSDN C0398650 Idiopathic thrombocytopenia purpura C0398623 Thrombophilia HSDN C4084774 Have weight loss C0018799 Heart diseases HSDN C0857305 Thrombocytopenia purpura C0796561 Melanoma vaccines HSDN C0151786 Weakness muscle C0023473 Myeloid leukemia, chronic HSDN C0010200 Cough symptom C0023890 Liver cirrhosis HSDN C0011168 Disorder deglutition C1336753 Thyroid lymphoma MalaCards C0013404 Respiratory difficulty C0011615 Dermatitis, atopic HSDN C0000727 Abdomen acute C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0349588 Stature short C0220666 Arthrogryposis multiplex congenita, distal, type iia MalaCards|HPO C2242996 Tingling C0012691 Dislocations HSDN C0011991 Loose stools C0020097 Htlv-i infections HSDN C1962972 Proteinuria adverse event C0025007 Measles HSDN C0013362 Dysarthrias C2984289 Melanoma pathway HSDN C0013604 Edematous C0040715 Chromosomal translocation HSDN C0020673 Hypothermia (central) (local) C0151516 Thyroid hypoplasia HPO C0522224 Palsied C0032227 Pleural effusion disorder HSDN C0086565 Liver function abnormal C0220710 Medium-chain acyl-coenzyme a dehydrogenase deficiency HPO C0041657 Consciousness loss C0011854 Diabetes mellitus, insulin-dependent HSDN C0005745 Blepharoptosis C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0007758 Cerebellar ataxia C0022821 Kyphosis deformity of spine HSDN C1963281 Vomiting adverse event C0034530 Injury radiation HSDN C4085211 Pain distress question C0002382 Alveolar bone loss HSDN C0151786 Weakness muscle C0015625 Fanconi anemia HSDN C0026838 Spasticity muscle C3714897 Spastic paraplegia 57, autosomal recessive MalaCards C0085650 Purpura fulminans C0006666 Calciphylaxes HSDN C4084773 Bothered by weight gain C0007121 Bronchogenic carcinoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003493 Aortic diseases HSDN C4085222 Nausea C0002726 Amyloidosis HSDN C0002962 Angina C1762616 Meningioma, benign, no icd-o subtype HSDN C0013390 Cramps menstrual C0037369 Smoking HSDN C0413252 Hypothermia due to exposure C0038525 Subarachnoid hemorrhage HSDN C2032396 Pelvic pain on the right C0020550 Hyperthyroidism HSDN C3714552 Strength decreased C0282207 Cronkhite-canada syndrome MalaCards|UMLS C0150055 Pain chronic C0013720 Ehlers-danlos syndrome HSDN C4084802 Usual severity diarrhea C2931788 Atypical hemolytic uremic syndrome MalaCards C0518090 Frequency of pain question C0026764 Multiple myeloma HSDN C2237041 Shox gene with short stature C0432443 Deletion of long arm of chromosome 18 OrphaNet|MalaCards C4084802 Usual severity diarrhea C1844663 Islets of langerhans, absence of HPO C0520909 Ponv C0020538 Hypertensive disease HSDN C0149793 Transient monocular blindness C0160680 Carotid artery injury HSDN C4085862 Bothered by nausea C0031511 Pheochromocytoma MalaCards C0242936 Center pain C0018203 Chronic granulomatous disease HSDN C0522224 Palsied C0002170 Alopecia HSDN C0015469 Facial paralysis C0042138 Uterine neoplasms HSDN C0015468 Face pain C0314657 Genetic predisposition HSDN C0917816 Deficiency mental C0796195 Waisman syndrome OrphaNet|HPO|MalaCards C0020903 Illusion C3542413 Cdisc adas-cog - comprehension HSDN C0030554 Abnormal sensation C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C3539891 Pelvic pain to the rear C0014179 Endometritis HSDN C1963281 Vomiting adverse event C0268293 Corticosterone methyl oxidase type i deficiency HPO C1384666 Decreased hearing C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C1963281 Vomiting adverse event C0036690 Septicemia HSDN C0036572 Convulsion C0003492 Aortic coarctation HSDN C0036572 Convulsion C1853205 Glycosylphosphatidylinositol deficiency MalaCards|HPO C0018681 Headache, cephalalgia C0004576 Babesiosis OrphaNet|MalaCards C0155502 Vertigo benign positional C0023702 Injury lightning HSDN C0018772 Deafness C2674706 Osteopenic nonfracture syndrome HPO C0030193 Sense of pain C0031941 Pineal gland neoplasm HSDN C0020580 Decreased sensation C0017409 Herpes zoster oticus HSDN C0042963 Symptoms vomiting C0008625 Chromosome aberrations HSDN C0002965 Crescendo angina C0344315 Depressed mood HSDN C3714552 Strength decreased C0017921 Glycogen storage disease type ii MalaCards|UMLS C3829611 Nausea frequency C0037937 Spine injury HSDN C3541349 Syncope C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards|HPO C0033774 Skin pruritus C0035436 Rheumatic fever HSDN C0042928 Paralysis vocal cord C1720922 Respiratory aspiration HSDN C3539891 Pelvic pain to the rear C1456865 Ureteral calculi HSDN C1963091 Diarrhea adverse event C0600564 Self-efficacy HSDN C0477491 Other urticaria C0042109 Urticaria UMLS C0005904 Alteration in body temperature C0020681 Sleep-related respiratory failure MalaCards C3641756 Have diarrhea C1420653 Tcn2 gene HPO C0013362 Dysarthrias C0206245 Amyloid neuropathies, familial MalaCards C0030552 Paralysis partial C0919267 Ovarian neoplasm HSDN C0022638 Ketosis C1833102 Diabetes mellitus, permanent neonatal, with neurologic features HPO C3539023 Pelvic pain increasing in frequency C0302148 Blood clot HSDN C0848203 Male pelvic pain C0032966 Complication, neoplastic pregnancy HSDN C0030193 Sense of pain C0086666 Preinfarction syndrome UMLS C1856661 Cornea cloudy C1849718 Popliteal pterygium syndrome, lethal type HPO C4085317 Diarrhea frequency C0036674 Sensory deprivation HSDN C0023015 Language handicap C0085541 Epilepsy, frontal lobe HSDN C3178766 Nociceptive pain C0004935 Animal ethology HSDN C1963281 Vomiting adverse event C0000814 Abortion, missed HSDN C0018991 Paralysis one side of body C3553788 Alternating hemiplegia of childhood 2 MalaCards C4084774 Have weight loss C0553580 Ewings sarcoma HSDN C0035229 Respiratory function impaired C2931047 Hecht scott syndrome OrphaNet C0233514 Behavior abnormal C1866983 Scleroderma, familial progressive MalaCards C2242996 Tingling C0033817 Pseudomonas infections HSDN C1579931 Depressed - symptom C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0016382 Cutaneous vascular engorgement C0220679 Ehlers-danlos syndrome, autosomal dominant, type unspecified OrphaNet C0750937 Appendicular ataxia C0007795 Diffuse cerebral sclerosis of schilder MalaCards C4085222 Nausea C0521607 Peritoneal fibrosis HSDN C1963281 Vomiting adverse event C3463824 Myelodysplastic syndrome HSDN C0020672 Body temperature decreased C0014544 Epilepsy HSDN C1962972 Proteinuria adverse event C0042487 Venous thrombosis HSDN C4084723 Constipation C0017612 Glaucoma, open-angle HSDN C0030552 Paralysis partial C0037304 Skull fracture HSDN C4085317 Diarrhea frequency C0040336 Tobacco use disorder HSDN C2096293 Ent surgical result ear vertigo C1552262 Nurse practitioner - family HSDN C2362324 Pediatric obesity C0032897 Prader-willi syndrome HSDN C2029884 Hearing loss by exam C0029878 Otitis externa HSDN C0242936 Center pain C0085084 Motor neuron disease HSDN C0349588 Stature short C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C2032396 Pelvic pain on the right C0038941 Incisional infection HSDN C0026821 Cramp C0037397 Behavior social HSDN C1549543 Administration method - pain C0011586 Three dimensional vision HSDN C0023012 Delay language C1860224 Ablepharon-macrostomia syndrome OrphaNet|HPO|MalaCards C4085661 Usual severity nausea C0036240 Response, satiety HSDN C0518090 Frequency of pain question C0679360 Foodborne disease HSDN C0036572 Convulsion C0003962 Ascites HSDN C0034150 Skin purpura C0014544 Epilepsy HSDN C3203358 Alveolar hypoventilation C4042784 Feeding and eating disorders HSDN C1963091 Diarrhea adverse event C0031149 Peritoneal neoplasms HSDN C0003862 Pain joint C0036864 Sexual relations HSDN C0085636 Light sensitivity C1864446 Retinitis pigmentosa 25 MalaCards C0018965 Blood urine C0039445 Hereditary hemorrhagic telangiectasia MalaCards|HPO C0040822 D tremors C0268386 Amyloid polyneuropathy, swiss type MalaCards C0040485 Wryneck C0019880 Homocystinuria HSDN C4085211 Pain distress question C0004626 Pneumonia, bacterial HSDN C0520909 Ponv C0007131 Non-small cell lung carcinoma HSDN C4085222 Nausea C0040479 Torsades de pointes HSDN C0030193 Sense of pain C0002438 Amebiasis HSDN C0033377 Caudal displacement C1876203 Frontonasal dysplasia MalaCards|HPO C2032395 Pelvic pain on the left C0016664 Fatigue fracture HSDN C0020796 Profoundly mentally retarded C2749019 Joubert syndrome 10 (disorder) MalaCards C0019825 Voice hoarseness C1302282 Chromaffin cell neoplasm MalaCards C4084774 Have weight loss C2931189 Neural crest tumor MalaCards C0030193 Sense of pain C0019156 Hepatic veno-occlusive disease HSDN C1565249 Limitation, mobility C0007959 Charcot-marie-tooth disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0042111 Urticaria pigmentosa OrphaNet|MalaCards C0684343 Pseudophakia C0010038 Corneal opacity HSDN C0727671 Red cross toothache drops C0027051 Myocardial infarction HSDN C0034150 Skin purpura C0006663 Calcinosis HSDN C3898969 Have been vomiting C0042331 Migraine variant MalaCards C4084723 Constipation C0026650 Movement disorders HSDN C3887638 Failure to thrive in infant C0432328 Xeroderma pigmentosum, variant form MalaCards C0036396 Sciatica C0752191 Central nervous system schistosomiasis HSDN C0848203 Male pelvic pain C0004935 Animal ethology HSDN C2984058 Have pain C0001327 Laryngitis acute HSDN C0012569 Double vision C0030297 Pancreatic neoplasm HSDN C0010520 Skin cyanosis C3244301 Coverage level - family HSDN C1527344 Dysphonia C0472522 Laryngoceles HSDN C0151889 Reflexes tendon increased C1835614 Hereditary hyperexplexia MalaCards C0424755 Fever symptoms C0002171 Alopecia areata HSDN C0007859 Pain neck C0042170 Uveomeningoencephalitic syndrome HSDN C0917816 Deficiency mental C0265221 Walker-warburg congenital muscular dystrophy MalaCards C0042571 Vertigo subjective C0026946 Mycoses HSDN C0000737 Abdomen pain C0242137 Typhus, tick MalaCards C0242936 Center pain C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C1549543 Administration method - pain C0013712 Ego HSDN C2024893 Cardiovascular surgery result: fatigue C0026272 Mixed connective tissue disease OrphaNet|MalaCards C4085222 Nausea C0013292 Obstruction duodenal HSDN C0031911 Pigment deposition C1832174 Doyne honeycomb retinal dystrophy MalaCards C1962972 Proteinuria adverse event C0011882 Diabetic neuropathies HSDN C0020578 Hyperventilate C0009241 Cognition disorders HSDN C4085317 Diarrhea frequency C1963211 Pericarditis adverse event HSDN C2700617 Irritation - emotion C0751291 Desmoplastic medulloblastoma MalaCards C1961131 Cough adverse event C0887976 Chlamydophila infections HSDN C2024878 Cardiovascular surgery result: dyspnea C0031046 Pericarditis HSDN C0013604 Edematous C0014527 Epidermolysis bullosa HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C4050613 Anxiety scale (basc-2) HSDN C0018772 Deafness C1414203 Dws gene HSDN C2024893 Cardiovascular surgery result: fatigue C2015933 Outcomes otolaryngology hearing HSDN C0522224 Palsied C0006840 Candidiasis HSDN C0027066 Myoclonic jerking C0031762 Photosensitivity disorders HSDN C0036572 Convulsion C0270823 Petit mal status UMLS C4085642 Level of joint stiffness C0175700 Multiple synostosis syndrome MalaCards C0030193 Sense of pain C0018418 Gynecomastia HSDN C3539889 Pelvic pain increasing in severity C0024141 Lupus erythematosus, systemic HSDN C0000737 Abdomen pain C1333307 Adenocarcinoma of distal 1/3 of common bile duct UMLS C0497247 Blood pressure elevation C0877024 Schimke immunoosseous dysplasia MalaCards|HPO C4084724 Usual severity constipation C2981150 Uranostaphyloschisis HSDN C4042891 Sleep wake disorders C0021799 Interprofessional relations HSDN C3146279 Coma C0220754 Biotinidase deficiency MalaCards|HPO C4084766 Vomiting C2931876 Hirschsprung disease 1 MalaCards C0040822 D tremors C1843884 Spinocerebellar ataxia 18 UMLS C4084769 Vomiting frequency C1704212 Embolism embolus HSDN C0019209 Large liver C0268540 Hhh syndrome HPO C4085210 Usual severity pain C0009763 Conjunctivitis HSDN C0860603 Anxiety symptom C3554605 Mc3dn2 MalaCards C0006370 Bulimia C0043097 Perception, weight HSDN C3898969 Have been vomiting C0031069 Familial mediterranean fever HSDN C1963071 Back pain adverse event C0015814 Femur head necrosis HSDN C3887638 Failure to thrive in infant C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011570 Mental depression HSDN C4084774 Have weight loss C0034885 Rectal neoplasms HSDN C0033774 Skin pruritus C1335317 Pancreatic signet ring cell carcinoma UMLS C0017181 Gastrointestinal bleed C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C4085548 Usual severity dizziness C0010674 Cystic fibrosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0269185 Uterus retroverted HSDN C0000731 Abdomen distention C1531773 Currarino triad MalaCards|HPO C0005745 Blepharoptosis C4015552 Fibrosis of extraocular muscles, congenital, 5 MalaCards C0015672 Decreased energy C0037579 Soft tissue neoplasms HSDN C0497247 Blood pressure elevation C3888104 Glomerulopathy with fibronectin deposits OrphaNet|HPO|MalaCards C0920505 Emotional shock C0700613 Anxiety state UMLS C0009398 Color vision defects C0024305 Lymphoma, non-hodgkin HSDN C0023380 Lethargy C1579931 Depressed - symptom HSDN C2911645 Weight loss adverse event C1963083 Cholecystitis adverse event HSDN C1279888 Proteinuria of undiagnosed cause C3495422 Finding relating to sexuality and sexual activity HSDN C0025287 Meningitis-like C0007785 Cerebral infarction HSDN C0349588 Stature short C0268647 Lysinuric protein intolerance MalaCards|HPO C0151889 Reflexes tendon increased C1838281 Fryns macrocephaly OrphaNet|MalaCards C0043094 Weight gain C1000587 Pemphigus HSDN C3274924 Have been coughing C0037930 Spinal cord neoplasms HSDN C1557397 Adverse event associated with pain C0009081 Congenital clubfoot HSDN C0009806 Constipate C0042338 Herpesvirus 3, human HSDN C0030552 Paralysis partial C1833373 Inclusion body myopathy, autosomal recessive MalaCards C0010200 Cough symptom C0006840 Candidiasis HSDN C0030193 Sense of pain C0860580 Medullary carcinoma of breast UMLS C0028738 Nystagmus C4014347 Pontocerebellar hypoplasia, type 10 MalaCards C0026838 Spasticity muscle C2677682 Rett syndrome, zappella variant HPO C2984058 Have pain C0023267 Fibroid tumor HSDN C0027497 Queasy C0267204 Drug-induced nausea and vomiting, nos UMLS C0018965 Blood urine C0019034 Hemoglobin sc disease MalaCards C0424755 Fever symptoms C0344311 Blister HSDN C4084767 Bothered by vomiting C0268573 Valinemia MalaCards C0231528 Muscle pain generalized C2930900 Beta-sarcoglycanopathy MalaCards C1565249 Limitation, mobility C0037051 Behavior illness HSDN C4084775 Usual severity weight loss C0010418 Cryptosporidiosis DiseaseOntology|HSDN C4085862 Bothered by nausea C0005779 Blood coagulation disorders HSDN C4085661 Usual severity nausea C0025345 Menstruation disturbances HSDN C0002962 Angina C0037304 Skull fracture HSDN C0234512 Prosopagnosia C0038551 Stimulation, subliminal HSDN C0004604 Pain back C0007095 Carcinoid tumor HSDN C3496180 Sleep apnea C0002736 Amyotrophic lateral sclerosis MalaCards C4084773 Bothered by weight gain C0027902 Neuropsychological diagnosis HSDN C0010200 Cough symptom C0037355 Smallpox vaccines HSDN C4085548 Usual severity dizziness C0007789 Cerebral palsy HSDN C0030193 Sense of pain C0349622 Hemangiopericytoma of meninges HSDN C4085661 Usual severity nausea C0205770 Choroid plexus papilloma HPO C0009398 Color vision defects C1423541 Vangl2 gene HSDN C0018772 Deafness C0003850 Arteriosclerosis HSDN C0242936 Center pain C0235833 Congenital diaphragmatic hernia HSDN C0009806 Constipate C0220769 Fg syndrome MalaCards|HPO|UMLS C0151889 Reflexes tendon increased C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C0013362 Dysarthrias C1969796 Ataxia, spastic, 2, autosomal recessive (disorder) MalaCards|HPO C4084725 Usual severity cough C1090821 Sepsis (invertebrate) HSDN C4085317 Diarrhea frequency C0024215 Lymphangiectasis, intestinal OrphaNet|MalaCards C0013604 Edematous C0020540 Malignant hypertension HSDN C4085317 Diarrhea frequency C0005941 Bone diseases, developmental HSDN C0036572 Convulsion C3495023 Epilepsia partialis continua, non-refractory UMLS C4084768 Usual severity vomiting C0018567 Hand dermatoses HSDN C0746674 Muscle weakness generalized C2931347 Cardiac form of generalized glycogenosis MalaCards C1549543 Administration method - pain C1956089 Osteophyte HSDN C0042571 Vertigo subjective C0013806 Electroplexy shock therapy HSDN C0023012 Delay language C3150928 Nf1 microdeletion syndrome MalaCards|HPO C0241137 Skin pallor C0748400 Rh disease MalaCards C1961131 Cough adverse event C0003469 Anxiety disorders HSDN C0030554 Abnormal sensation C3888109 Acromelalgia hereditary MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0037774 Spatial behavior HSDN C3829611 Nausea frequency C0019054 Hemolysis (disorder) HSDN C1557397 Adverse event associated with pain C0206681 Adenocarcinoma, clear cell HSDN C4085548 Usual severity dizziness C0042373 Vascular diseases HSDN C4084776 Weight loss C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C1963249 Tinnitus adverse event C3542996 Mindfulness HSDN C0028738 Nystagmus C0266526 Norrie disease OrphaNet|HPO|MalaCards C4084725 Usual severity cough C0012691 Dislocations HSDN C2984058 Have pain C0003614 Appendiceal neoplasms HSDN C0000727 Abdomen acute C1963119 Stomach ulcer adverse event HSDN C0264611 Apraxia of speech C0016952 Galactosemias MalaCards C0518090 Frequency of pain question C0041325 Peritonitis, tuberculous MalaCards|HSDN C4084723 Constipation C0004623 Bacterial infections HSDN C0036572 Convulsion C0086922 Purpura rheumatoid MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2984572 Malaria pathway HSDN C0011991 Loose stools C0018790 Cardiac arrest HSDN C2911645 Weight loss adverse event C0038186 Reflex, startle HSDN C2024893 Cardiovascular surgery result: fatigue C1304456 Congo hemorrhagic fever MalaCards C0000737 Abdomen pain C0022410 Joint instability HSDN C0011168 Disorder deglutition C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C3541349 Syncope C0013295 Duodenal ulcer HSDN C2315100 Pediatric failure to thrive C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C4084723 Constipation C0020598 Hypocalcemia HSDN C0020455 Hypergammaglobulinemia C1850568 Nakajo syndrome MalaCards|HPO C0026826 High muscle tone C0026769 Multiple sclerosis HSDN C0013362 Dysarthrias C3554690 Ataxia-oculomotor apraxia 3 MalaCards C3463815 Feel fatigue C0162316 Iron deficiency anemia HSDN C2237041 Shox gene with short stature C0265962 Ichthyosis linearis circumflexa MalaCards|HPO C4085549 Dizziness C0524620 Metabolic syndrome x HSDN C3898969 Have been vomiting C0022758 Kap HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007273 Carotid artery diseases HSDN C0242936 Center pain C0001627 Congenital adrenal hyperplasia HSDN C0018932 Bright red rectal bleeding C1335686 Neuroendocrine neoplasm of rectum MalaCards C1963093 Dizziness adverse event C0305062 Tetanus toxoids HSDN C0920033 Cardiopulmonary insufficiency C1444565 Cardiorespiratory failure UMLS C0019079 Bloody sputum C1708769 Lung clear cell adenocarcinoma UMLS C0024031 Back pain lower back C1704421 Skin pigmentation disorder HSDN C1963184 Nystagmus adverse event C1275081 Cardio-facio-cutaneous syndrome OrphaNet|HPO C0030193 Sense of pain C0014356 Enterocolitis HSDN C0012833 Dizzy C0010709 Cyst HSDN C0016199 Pain flank C0006288 Bronchopulmonary sequestration HSDN C1384666 Decreased hearing C0010273 Craniofacial dysostosis MalaCards|HSDN|HPO C2024893 Cardiovascular surgery result: fatigue C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0020649 Blood pressure decreased C0032001 Pituitary apoplexy OrphaNet|MalaCards C2911647 Weight gain adverse event C0024841 Matrimony, matrimonial HSDN C0018772 Deafness C0034088 Pulmonary valve insufficiency HSDN C0026838 Spasticity muscle C0008058 Chilblains HSDN C0013595 Eczematous dermatitis C0032027 Pityriasis rubra pilaris MalaCards|HPO C0917816 Deficiency mental C0010276 Craniopharyngioma MalaCards|HPO C0008031 Pain chest C0003811 Cardiac arrhythmia HSDN C4084727 Cough frequency C0008925 Cleft palate HSDN C1963281 Vomiting adverse event C1837218 Cleft palate, isolated HSDN C3274924 Have been coughing C0027627 Neoplasm metastasis HSDN C0454644 Delayed language development C3495551 Dihydropyrimidinuria MalaCards C0018926 Emesis bloody C0085411 Angiodysplasia HSDN C1963184 Nystagmus adverse event C0751603 Autosomal recessive hereditary spastic paraplegia MalaCards C3274924 Have been coughing C1457883 Aggressive reaction HSDN C0017672 Pain tongue C0006840 Candidiasis HSDN C1549543 Administration method - pain C0206633 Angiomyolipoma HSDN C0009806 Constipate C0677948 Stage ii colorectal cancer UMLS C4084788 Have dizziness C0343633 Brazilian haemorrhagic fever MalaCards C0042024 Urine incontinence C1527348 Brain hypoxia HSDN C0497406 Over weight C0012691 Dislocations HSDN C0027066 Myoclonic jerking C0034341 Pyruvate carboxylase deficiency disease HSDN C0030193 Sense of pain C0013808 Electroconvulsive therapy HSDN C0007758 Cerebellar ataxia C1568249 Usher syndrome, type ii MalaCards|HPO C4049602 Hyperactivity C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0032617 High urine output C2909036 Twin twin transfusion HSDN C0036572 Convulsion C2349436 Migraine triggered seizures UMLS C4042891 Sleep wake disorders C0039231 Tachycardia HSDN C0085631 Abnormal excitement C0236969 Substance-related disorders HSDN C4084725 Usual severity cough C0205788 Histiocytoid hemangioma HSDN C0013595 Eczematous dermatitis C0020757 Ichthyoses MalaCards C1557397 Adverse event associated with pain C0024720 Anxiety scale, manifest HSDN C0036572 Convulsion C0268263 Multiple sulfatase deficiency disease OrphaNet|HPO|MalaCards C0237326 Defecation pain C3203358 Hypoventilation MalaCards C4084769 Vomiting frequency C0018799 Heart diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085399 Ehrlichiosis HSDN C1963065 Apnea adverse event C3810814 Myocardial infarction ecg assessment HSDN C0030552 Paralysis partial C1862937 Ftdals1 MalaCards|HPO C0424755 Fever symptoms C0008350 Cholelithiasis HSDN C0018681 Headache, cephalalgia C0477374 Other specified headache syndromes UMLS C0030193 Sense of pain C1511304 Breast carcinoma with osteoclastic giant cells UMLS C0013404 Respiratory difficulty C0175704 Leopard syndrome HSDN C0040822 D tremors C0039082 Syndrome HSDN C0423719 Central post stroke pain C1536114 Central pain syndrome UMLS C0030552 Paralysis partial C0001807 Aggressive behavior HSDN C0030486 Extremity paralysis, lower C0520679 Sleep apnea, obstructive HSDN C1963252 Tremor adverse event C1546847 Entity name part type - family HSDN C2024893 Cardiovascular surgery result: fatigue C0014556 Epilepsy, temporal lobe HSDN C0518090 Frequency of pain question C0016124 Finger injury HSDN C1384666 Decreased hearing C0016037 Fibrodysplasia ossificans progressiva OrphaNet|HPO|MalaCards C4084725 Usual severity cough C2981150 Uranostaphyloschisis HSDN C4085210 Usual severity pain C0178324 Blood vessel injury HSDN C0557874 Global developmental delay C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO C4084897 Sleep disturbance subordinate domain C3151781 Ck syndrome MalaCards|HPO C0036572 Convulsion C2678263 Methylmalonic acidemia, cblh type, formerly HPO C0857305 Thrombocytopenia purpura C0017665 Membranous glomerulonephritis HSDN C4084768 Usual severity vomiting C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C4085548 Usual severity dizziness C0205788 Histiocytoid hemangioma HSDN C0427055 Face weakness C0393551 Madras-type motor neurone disease MalaCards C0086437 Joint hypermobility C0795887 Chromosome xp21 deletion syndrome MalaCards C0011175 Deficient fluid volume C0852654 21-hydroxylase deficiency MalaCards C4084776 Weight loss C0848377 Trauma to the abdomen HSDN C1838869 Proximal neurogenic muscle weakness C0036202 Sarcoidosis MalaCards|HPO C4084725 Usual severity cough C0023048 Creeping eruptions HSDN C0042024 Urine incontinence C0032584 Polyps HSDN C0020458 Hyperhydrosis C0795878 Monosomy 22 MalaCards C0028961 Urine output decreased C2936209 Conducted energy weapon injuries HSDN C1557397 Adverse event associated with pain C0311277 Obesity, abdominal HSDN C0152227 Tearing excessive C1852555 Corneal endothelial dystrophy 1, autosomal dominant MalaCards C2911645 Weight loss adverse event C0011265 Presenile dementia HSDN C0026826 High muscle tone C0026034 Microstomia HSDN C0009806 Constipate C1333865 Grade 2 rectal adenocarcinoma UMLS C0019079 Bloody sputum C0039263 Takayasu arteritis MalaCards|HPO C0031911 Pigment deposition C0162834 Hyperpigmentation MalaCards C4085210 Usual severity pain C0001627 Congenital adrenal hyperplasia HSDN C0000737 Abdomen pain C0854783 Stage iii rectosigmoid cancer UMLS C0152459 Striae C0001618 Tumors of adrenal cortex HSDN C0857305 Thrombocytopenia purpura C0006434 Burn injury HSDN C0151786 Weakness muscle C0033817 Pseudomonas infections HSDN C2984057 Have nausea C1546635 Specimen source codes - fistula HSDN C4085317 Diarrhea frequency C0039240 Supraventricular tachycardia HSDN C3898969 Have been vomiting C0031039 Effusion pericardial HSDN C2919142 Short stature adverse event C3888212 Seckel syndrome 4 MalaCards C0013528 Echo speech C1851708 Encephalopathy, recurrent, of childhood MalaCards C0042963 Symptoms vomiting C1845862 Creatine deficiency, x-linked MalaCards|HPO|UMLS C3463815 Feel fatigue C0085404 Poems syndrome MalaCards C0242936 Center pain C0033680 Protein-losing enteropathies HSDN C0024031 Back pain lower back C0238156 Hematoma, subdural, intracranial HSDN C0151908 Dry skin C0263465 Asteatosis cutis UMLS C0557874 Global developmental delay C0342731 Deficiency of mevalonate kinase OrphaNet|HPO|MalaCards C0031911 Pigment deposition C0496836 Malignant tumor of eye MalaCards C4084776 Weight loss C1547044 Kind of quantity - smell HSDN C4084725 Usual severity cough C0006118 Brain neoplasms HSDN C4084784 Diarrhea C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C0018524 Hallucinate C0015397 Disorder of eye HSDN C2911647 Weight gain adverse event C0007193 Cardiomyopathy, dilated HSDN C0398650 Idiopathic thrombocytopenia purpura C0032788 Postoperative hemorrhage HSDN C3146279 Coma C3810814 Myocardial infarction ecg assessment HSDN C0030554 Abnormal sensation C0458219 Complex regional pain syndromes HSDN C0004604 Pain back C0026975 Myelitis HSDN C0850758 Pain pelvic C1458155 Mammary neoplasms HSDN C2919142 Short stature adverse event C2020284 Stickler syndrome, type 1 MalaCards C0043068 Friderichsen-waterhouse syndrome C0032308 Staphylococcal pneumonia HSDN C0234146 Absent reflex C3151753 Combined oxidative phosphorylation deficiency 6 MalaCards C0022408 Disorder joint C1866985 Early balding, patella luxation, acromicria, and hypogonadism MalaCards C0039070 Collapse fleeting C0950124 Papillomavirus infections HSDN C0007758 Cerebellar ataxia C0751383 Juvenile neuronal ceroid lipofuscinosis OrphaNet|MalaCards C0018784 Deafness sensorineural C1857333 Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia OrphaNet|MalaCards C0042928 Paralysis vocal cord C0032965 Pregnancy complications, infectious HSDN C0024031 Back pain lower back C0009404 Colorectal neoplasms HSDN C0042963 Symptoms vomiting C0700327 Clinical findings relating to memory HSDN C0039870 Leanness C0033968 Psychotherapeutic technique HSDN C0231528 Muscle pain generalized C0270959 Myotonia levior HPO C0002962 Angina C0033586 Failure, prosthesis HSDN C1579931 Depressed - symptom C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0018946 Hematoma, subdural HSDN C0086437 Joint hypermobility C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0018681 Headache, cephalalgia C0042514 Tachycardia, ventricular HSDN C0151786 Weakness muscle C0039292 Tangier disease HSDN C0557874 Global developmental delay C0266484 Schizencephaly OrphaNet|HPO|MalaCards C0728710 Pupil constriction observed C0040997 Trigeminal neuralgia HSDN C1963180 Neck pain adverse event C0005937 Bone cysts HSDN C0033774 Skin pruritus C0062527 Hepatitis b vaccine HSDN C1963184 Nystagmus adverse event C0266526 Norrie disease OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0020488 Hypernatremia HSDN C4084776 Weight loss C0018800 Cardiomegaly HSDN C0030193 Sense of pain C0423705 Other specified trigeminal neuralgia UMLS C0007758 Cerebellar ataxia C0206734 Hemangioblastoma HSDN C0014089 Functional encopresis C0013336 Dwarfism HSDN C1579931 Depressed - symptom C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C2911647 Weight gain adverse event C0017638 Glioma HSDN C0007758 Cerebellar ataxia C0239981 Hypoalbuminemia HSDN C0013404 Respiratory difficulty C0079631 Interdisciplinary communication HSDN C0013604 Edematous C0021361 Female infertility HSDN C1263846 Attention deficit disorder with hyperactivity C0342853 Sialuria OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0001726 Affective symptoms HSDN C0013404 Respiratory difficulty C0007785 Cerebral infarction HSDN C0042571 Vertigo subjective C0403447 Chronic kidney insufficiency HSDN C1836296 Lower extremity weakness C3711370 Spastic paraplegia type 7 MalaCards C0040822 D tremors C0700595 Spinal muscular atrophies of childhood HSDN C0221166 Paraparesis C0085762 Alcohol abuse UMLS C1963093 Dizziness adverse event C0013080 Down syndrome HSDN C0151786 Weakness muscle C0752181 Central nervous system parasitic infections HSDN C1963093 Dizziness adverse event C1527336 Sjogren's syndrome HSDN C0011991 Loose stools C0553580 Ewings sarcoma HSDN C1519353 Skin eruption papular C1959582 Pten hamartoma tumor syndrome OrphaNet|MalaCards C4085210 Usual severity pain C1253943 Fluid in the chest HSDN C1145670 Failure respiratory C2930851 Intestinal lipophagic granulomatosis MalaCards C4085211 Pain distress question C0009952 Febrile convulsions HSDN C2242996 Tingling C0018920 Hemangioma, cavernous HSDN C0151889 Reflexes tendon increased C3711370 Spastic paraplegia type 7 MalaCards C4084776 Weight loss C2984302 Leishmaniasis infection pathway HSDN C0034155 Thrombotic thrombocytopenic purpura C0014544 Epilepsy HSDN C4084802 Usual severity diarrhea C0042870 Vitamin d deficiency HSDN C4085661 Usual severity nausea C0456892 Csf low pressure HSDN C0036572 Convulsion C0026590 Child mother relationship HSDN C2911645 Weight loss adverse event C0034531 Experimental radiation injuries HSDN C0018808 Murmur C0035229 Respiratory insufficiency HSDN C4084788 Have dizziness C0338480 Common migraine HSDN C1557397 Adverse event associated with pain C0035585 Rickettsia infections HSDN C3815497 Cough C0018273 Growth disorders HSDN C0018772 Deafness C0016045 Fibroma HSDN C0000737 Abdomen pain C0278696 Childhood hepatoma, group i UMLS C4084776 Weight loss C0008325 Cholecystitis HSDN C2203646 Jaundice C0013502 Echinococcosis HSDN C0857305 Thrombocytopenia purpura C0016397 Focal infection HSDN C0020580 Decreased sensation C0751799 Brain hemorrhage, traumatic HSDN C0413252 Hypothermia due to exposure C0036439 Scoliosis, unspecified HSDN C1961131 Cough adverse event C0018939 Hematological disease HSDN C1963071 Back pain adverse event C0013922 Embolism HSDN C3539020 Pelvic pain decreasing in frequency C0016548 Foreign body migration HSDN C0040485 Wryneck C3538999 Dystonia 23 MalaCards|UMLS C0151686 Growth retardation C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C1962972 Proteinuria adverse event C0014118 Endocarditis HSDN C0007166 Cardiac output decreased C0004623 Bacterial infections HSDN C4084775 Usual severity weight loss C1136321 Hiv-associated lipodystrophy syndrome HSDN C0020305 Fetal edema C0004775 Bartter disease HSDN C0151686 Growth retardation C3469542 Fanconi anemia, complementation group p MalaCards C0009806 Constipate C0005686 Urinary bladder diseases HSDN C0024031 Back pain lower back C0006145 Breast diseases HSDN C4084773 Bothered by weight gain C0035459 Atrophic rhinitis HSDN C3539895 Pelvic pain occurs with bowel movement C0007527 Cecal disease HSDN C4084776 Weight loss C0035228 Respiratory hypersensitivity HSDN C0015469 Facial paralysis C1333989 Familial meningioma MalaCards C4084769 Vomiting frequency C0004048 Breathing HSDN C0242936 Center pain C0019557 Hip fx HSDN C2911645 Weight loss adverse event C0013502 Echinococcosis HSDN C4085211 Pain distress question C0039131 Syphilis congenital HSDN C0040485 Wryneck C0020498 Ankylosing hyperostosis vertebral HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003492 Aortic coarctation HSDN C3541349 Syncope C0017636 Glioblastoma HSDN C0557874 Global developmental delay C4015242 Retinal dystrophy, juvenile cataracts, and short stature syndrome MalaCards C1961131 Cough adverse event C0151744 Myocardial ischemia HSDN C0018926 Emesis bloody C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0812426 Kidney problem C0748331 Renal transplant graft failure UMLS C2712367 Other speech disturbances C0013362 Dysarthria UMLS C0030552 Paralysis partial C0003504 Aortic valve insufficiency HSDN C0033774 Skin pruritus C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C3829611 Nausea frequency C0086543 Cataract nos HSDN C3539023 Pelvic pain increasing in frequency C0007097 Carcinomas HSDN C0857305 Thrombocytopenia purpura C0035053 Spontaneous remission HSDN C2911647 Weight gain adverse event C0264766 Rheumatic mitral stenosis HSDN C0041834 Erythematous condition C1260961 Lipoatrophia semicircularis MalaCards C2024893 Cardiovascular surgery result: fatigue C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C0018772 Deafness C0007097 Carcinomas HSDN C0020903 Illusion C0600564 Self-efficacy HSDN C2984058 Have pain C0029440 Osteoma HSDN C0007758 Cerebellar ataxia C1963138 Hypertension adverse event HSDN C4084784 Diarrhea C0038436 Post-traumatic stress disorder HSDN C1963184 Nystagmus adverse event C0339527 Leber congenital amaurosis OrphaNet|HPO|MalaCards C0019079 Bloody sputum C0004044 Asphyxia HSDN C2315100 Pediatric failure to thrive C0796004 Kabuki make-up syndrome OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0024299 Lymphoma HSDN C1963281 Vomiting adverse event C0595812 Fistula route HSDN C0009676 Confusion state C0024115 Lung diseases HSDN C0013404 Respiratory difficulty C1970470 Surfactant metabolism dysfunction, pulmonary, 2 (disorder) MalaCards|UMLS C0349588 Stature short C3810012 Rienhoff syndrome MalaCards C0233514 Behavior abnormal C0020497 Cortical congenital hyperostosis OrphaNet|HPO|MalaCards C0013604 Edematous C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2114287 Prepubertal vaginal bleeding C2979982 Vaginal hemorrhage UMLS C0036572 Convulsion C1336536 Supratentorial glioblastoma UMLS C2957106 Headache severe C0014078 Venezuelan equine encephalomyelitis DiseaseOntology|MalaCards C0010520 Skin cyanosis C1522133 High cholesterol level HSDN C1963170 Hypothermia adverse event C0023467 Leukemia, myelocytic, acute HSDN C4084766 Vomiting C0016510 Foot diseases HSDN C0013421 Dystonia C0022701 Kinesthesia HSDN C3815497 Cough C0748164 Pulmonary nodule multiple HSDN C0349588 Stature short C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C4085211 Pain distress question C0011606 Exfoliative dermatitis HSDN C1565249 Limitation, mobility C3887662 Intraspinal neoplasm HSDN C2315100 Pediatric failure to thrive C0270726 Alexander disease OrphaNet|HSDN|MalaCards C1963091 Diarrhea adverse event C0039614 Tetanus HSDN C0242936 Center pain C0151740 Intracranial hypertension HSDN C1962972 Proteinuria adverse event C0032965 Pregnancy complications, infectious HSDN C0014591 Bleeding nose C1527406 Rhizomelic pseudopolyarthritis MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0585442 Osteosarcoma of bone HSDN C2024893 Cardiovascular surgery result: fatigue C3714644 Thymus neoplasms MalaCards C0497247 Blood pressure elevation C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0270948 Neurogenic muscular atrophy C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0020455 Hypergammaglobulinemia C0085436 Meningitis, cryptococcal HSDN C2911645 Weight loss adverse event C0040456 Tooth impaction HSDN C2911647 Weight gain adverse event C1285666 Drinking behavior HSDN C0032227 Effusion pleural C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C1549543 Administration method - pain C0027859 Acoustic neuroma HSDN C0011991 Loose stools C0872315 Communicable diseases emerging HSDN C0242936 Center pain C0027697 Nephritis HSDN C0030552 Paralysis partial C1856306 Gsd iv, neuromuscular form, adult, with isolated myopathy HPO C0008031 Pain chest C1709572 Pleural desmoplastic mesothelioma UMLS C0026838 Spasticity muscle C0016719 Friedreich ataxia HPO C0000737 Abdomen pain C0997768 Glaucoma HSDN C0007859 Pain neck C0314657 Genetic predisposition HSDN C1961131 Cough adverse event C0021368 Inflammation HSDN C0206146 Myocardial stunning C0007194 Hypertrophic cardiomyopathy HSDN C0018965 Blood urine C2930815 Acute cerebral gaucher disease MalaCards C0018991 Paralysis one side of body C0006309 Brucellosis HSDN C0020649 Blood pressure decreased C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C0518090 Frequency of pain question C0085632 Apathy HSDN C0030193 Sense of pain C1333936 Adenoid cystic carcinoma of hard palate UMLS C0015672 Decreased energy C1334928 Necrotic changes (finding) HSDN C4084724 Usual severity constipation C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0234428 Consciousness disturbance C0039263 Takayasu arteritis MalaCards|HPO C0518090 Frequency of pain question C2939156 Development of sexuality HSDN C0020903 Illusion C0006109 Brain damage, chronic HSDN C1963252 Tremor adverse event C0085094 Head injury closed HSDN C0557874 Global developmental delay C2751320 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay MalaCards|HPO C0018965 Blood urine C1961835 Gaucher disease, type 1 MalaCards|HPO C0042940 Disorder of voice C0012746 Dissociative disorder HSDN C0042928 Paralysis vocal cord C0014866 Esophageal stenosis HSDN C0085649 Edema extremities C0085083 Ovarian hyperstimulation syndrome MalaCards|HPO C0237326 Defecation pain C0206247 Amyloid neuropathies MalaCards C4084773 Bothered by weight gain C0011848 Diabetes insipidus HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1546654 Specimen source codes - granuloma HSDN C3665492 Pigmentations C3645711 Congenital osteopetrosis MalaCards C2032396 Pelvic pain on the right C0022865 Obstetric labor complications HSDN C0035232 Diaphragmatic paralysis C2748608 Lead poisoning, susceptibility to HPO C0010200 Cough symptom C0919267 Ovarian neoplasm HSDN C0029163 Hemorrhage mouth C1962954 Cheilitis adverse event HSDN C0460137 Push down or depress C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C3815497 Cough C0878555 Diffuse panbronchiolitis MalaCards C0007166 Cardiac output decreased C0038356 Stomach neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0005426 Biliary tract neoplasm HSDN C0242936 Center pain C0030583 Parotitis HSDN C0019572 Hairiness C0019080 Hemorrhage HSDN C0857305 Thrombocytopenia purpura C0024232 Lymphatic metastasis HSDN C0013421 Dystonia C0036341 Schizophrenia HSDN C0278147 Nerve root pain C0003708 Arachnitis MalaCards C0242936 Center pain C0023281 Leishmaniasis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085404 Poems syndrome MalaCards|HSDN C0027066 Myoclonic jerking C2677590 Congenital disorder of glycosylation, type in MalaCards|HPO|UMLS C2315100 Pediatric failure to thrive C4015062 Combined oxidative phosphorylation deficiency 22 MalaCards C4085549 Dizziness C0021361 Female infertility HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0031154 Peritonitis HSDN C3815497 Cough C3489393 Hiatal hernia HSDN C0349588 Stature short C1832439 Mievis verellen-dumoulin syndrome OrphaNet|MalaCards C1963091 Diarrhea adverse event C0034088 Pulmonary valve insufficiency HSDN C4084784 Diarrhea C0518449 Control of hip fracture risk HSDN C0018772 Deafness C0032787 Postoperative complications HSDN C0034150 Skin purpura C0008533 Hemophilia b HSDN C0042963 Symptoms vomiting C1962983 Cataract adverse event HSDN C0040264 Ear ringing sound C0038186 Reflex, startle HSDN C4085210 Usual severity pain C0001622 Adrenal gland hyperfunction HSDN C1963091 Diarrhea adverse event C0041954 Ureteral diseases and syndromes HSDN C0043094 Weight gain C0001726 Affective symptoms HSDN C0003862 Pain joint C0023281 Leishmaniasis OrphaNet|MalaCards C1963091 Diarrhea adverse event C0025281 Meniere disease HSDN C0004604 Pain back C0009241 Cognition disorders HSDN C4085549 Dizziness C2240374 Eosinophil count raised HSDN C0036396 Sciatica C0919267 Ovarian neoplasm HSDN C0012833 Dizzy C0014836 Escherichia coli infections HSDN C0030193 Sense of pain C0041341 Tuberous sclerosis HSDN C1963093 Dizziness adverse event C0024530 Malaria HSDN C1549543 Administration method - pain C0039130 Cardiovascular syphilis HSDN C0033377 Caudal displacement C1276035 Pena-shokeir syndrome type i MalaCards|HPO C4085548 Usual severity dizziness C0038661 Suicide HSDN C4049644 Depression C1847987 Huntington disease-like 2 MalaCards|HPO C4085211 Pain distress question C2963140 Arteriovenous fistula in use with two needles HSDN C0231835 Respiration rate increased C0001255 Actinomycetales infections HSDN C4084769 Vomiting frequency C0035305 Retinal detachment HSDN C3539020 Pelvic pain decreasing in frequency C0042341 Varicocele HSDN C0042963 Symptoms vomiting C0276357 Swine influenza MalaCards C1557397 Adverse event associated with pain C0041312 Tuberculosis git nos HSDN C2203646 Jaundice C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C0522224 Palsied C0014053 Encephalitis, california DiseaseOntology|MalaCards C0007758 Cerebellar ataxia C0268228 Neuraminidase 1 deficiency OrphaNet C4084774 Have weight loss C1546747 Specimen source codes - polyps HSDN C0011991 Loose stools C1548484 Rheumatic fever vaccine HSDN C4084802 Usual severity diarrhea C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C4084724 Usual severity constipation C1962963 Osteoporosis adverse event HSDN C0042928 Paralysis vocal cord C0020615 Hypoglycemia HSDN C0015970 Fever unknown origin C0014836 Escherichia coli infections HSDN C0009806 Constipate C2217039 Stage iiic colon cancer UMLS C2911647 Weight gain adverse event C0043049 Water intoxication HSDN C0518090 Frequency of pain question C0018552 Hamartoma HSDN C0015469 Facial paralysis C0037286 Skin neoplasms HSDN C0085631 Abnormal excitement C1832884 Hemiplegic migraine, familial type 1 MalaCards|HPO C0018772 Deafness C0018805 Heart injuries HSDN C0034155 Thrombotic thrombocytopenic purpura C1963229 Retinal detachment adverse event HSDN C4084769 Vomiting frequency C0221074 Depression, postpartum HSDN C4085210 Usual severity pain C0036631 Seminoma HSDN C0028961 Urine output decreased C0869332 Of water deprivation HSDN C0011991 Loose stools C1857231 Lactase persistence HPO C0151786 Weakness muscle C1423541 Vangl2 gene HSDN C3887638 Failure to thrive in infant C2931653 Petty laxova wiedemann syndrome OrphaNet C0015672 Decreased energy C1553188 Hemolysis - observation HSDN C4084775 Usual severity weight loss C0011581 Depressive disorder HSDN C0026821 Cramp C0015624 Fanconi syndrome HPO C4085317 Diarrhea frequency C0011633 Dermatomyositis HSDN C0020673 Hypothermia (central) (local) C0032343 Poisoning HSDN C4084802 Usual severity diarrhea C1145670 Respiratory failure HSDN C4084767 Bothered by vomiting C1548484 Rheumatic fever vaccine HSDN C1962972 Proteinuria adverse event C0022104 Irritable bowel syndrome HSDN C1260880 Nasal drip C0280381 Lymphoepithelioma of the nasopharynx, stage ii UMLS C1579931 Depressed - symptom C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0427190 Ataxia, truncal C3150998 Spinocerebellar ataxia, autosomal recessive 10 MalaCards|HPO|UMLS C4084776 Weight loss C0027583 Nematode infections HSDN C4084784 Diarrhea C0041954 Ureteral diseases and syndromes HSDN C4084725 Usual severity cough C1704272 Benign prostatic hyperplasia HSDN C0020672 Body temperature decreased C0004943 Behcet syndrome HSDN C0013404 Respiratory difficulty C0042138 Uterine neoplasms HSDN C1962972 Proteinuria adverse event C0026850 Muscular dystrophy HSDN C0271215 Blindness legal C1832162 Hypotrichosis, congenital, with juvenile macular dystrophy OrphaNet|HPO|MalaCards C0267373 Bleeding intestine C1384687 Ancylostomiasis due to ancylostoma duodenale MalaCards C2024878 Cardiovascular surgery result: dyspnea C0004763 Barrett esophagus HSDN C3541349 Syncope C0021655 Insulin resistance HSDN C0241210 Speaking delay C0022340 Late-infantile neuronal ceroid lipfuscinosis MalaCards|HPO C0518090 Frequency of pain question C3668816 Inflammation of non-human mammary gland HSDN C0023380 Lethargy C0085409 Polyendocrinopathies, autoimmune HSDN C0497247 Blood pressure elevation C3149695 Melorheostosis with osteopoikilosis MalaCards|HPO C0013404 Respiratory difficulty C1336130 Stage ib adenosquamous cell carcinoma of lung UMLS C0557874 Global developmental delay C3810023 Verheij syndrome MalaCards C0242843 Sweating sickness C0003175 Anthrax disease HSDN C4085211 Pain distress question C0032763 Post gastrectomy syndrome HSDN C1963065 Apnea adverse event C0003507 Aortic valve stenosis HSDN C0004941 Behavioral symptoms C1850627 Keipert syndrome MalaCards C3539889 Pelvic pain increasing in severity C0314657 Genetic predisposition HSDN C2936821 Spinal cerebrospinal fluid leak C0037944 Spinal stenosis HSDN C0018681 Headache, cephalalgia C0026948 Mycosis fungoides HSDN C0020305 Fetal edema C1856305 Gsd iv, neuromuscular form, childhood MalaCards|HPO C2911647 Weight gain adverse event C0040046 Thrombophlebitis HSDN C0151786 Weakness muscle C0272126 Evans syndrome OrphaNet|MalaCards C1961131 Cough adverse event C2936664 Acquired hypogammaglobulinemia HSDN C0004604 Pain back C0023176 Lead poisoning HSDN C3641755 Have constipation C0019080 Hemorrhage HSDN C0398650 Idiopathic thrombocytopenia purpura C0272126 Evans syndrome MalaCards C0022346 Yellow skin C0001418 Adenocarcinoma HSDN C0026821 Cramp C0009404 Colorectal neoplasms HSDN C3898969 Have been vomiting C0015457 Expression facial HSDN C0041657 Consciousness loss C1145670 Respiratory failure HSDN C0020673 Hypothermia (central) (local) C0518450 Spinal fractures HSDN C1838869 Proximal neurogenic muscle weakness C1862372 Atypical osteomalacia involving the axial skeleton MalaCards C0426579 Anorexia symptom C0149573 Structure of posterior inferior cerebellar artery HSDN C0557874 Global developmental delay C2931009 Congenital disorder of glycosylation type 2d MalaCards C0026838 Spasticity muscle C1848922 Hexosaminidase alpha-subunit deficiency (variant b) OrphaNet|MalaCards C0000737 Abdomen pain C0028738 Nystagmus HSDN C0009398 Color vision defects C0019080 Hemorrhage HSDN C2911647 Weight gain adverse event C0008066 Child behavior disorders HSDN C1963091 Diarrhea adverse event C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C1963064 Anxiety adverse event C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C0003811 Cardiac rhythm disturbance C1836704 Arrhythmogenic right ventricular dysplasia, familial, 7 MalaCards C2315100 Pediatric failure to thrive C0687720 Central diabetes insipidus OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0751837 Gait ataxic C0524812 Intracranial hypotension HSDN C0013604 Edematous C0008533 Hemophilia b HSDN C0010200 Cough symptom C1879591 Lung adenocarcinoma with mixed bronchioloalveolar and invasive components UMLS C4084767 Bothered by vomiting C0027809 Neurilemmoma HSDN C1557397 Adverse event associated with pain C0205788 Histiocytoid hemangioma HSDN C0151686 Growth retardation C1997910 Citrin deficiency MalaCards C0460137 Push down or depress C1834570 Myoclonic dystonia HPO C4084727 Cough frequency C0009324 Ulcerative colitis HSDN C0150055 Pain chronic C0152177 Trigeminal neuropathy HSDN C4084769 Vomiting frequency C3812171 Bradycardia by ecg finding HSDN C0042928 Paralysis vocal cord C0032962 Pregnancy complications HSDN C3641756 Have diarrhea C0014118 Endocarditis HSDN C0027066 Myoclonic jerking C1960676 Non-epileptic myoclonus UMLS C4084724 Usual severity constipation C2931294 Wiedemann grosse dibbern syndrome MalaCards C4084776 Weight loss C0020619 Hypogonadism HSDN C0015672 Decreased energy C1709570 Pleural biphasic mesothelioma UMLS C3665386 Abnormal vision C0265303 Acrocephalopolysyndactyly type iv MalaCards C0413252 Hypothermia due to exposure C0038587 Substance withdrawal syndrome HSDN C0026838 Spasticity muscle C0035435 Rheumatism HSDN C0241157 Skin pustule C1864997 Majeed syndrome OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C3489787 Pituitary hormone deficiency, combined, 3 MalaCards C4084766 Vomiting C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0020505 Excessive eating C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0042963 Symptoms vomiting C0752165 Angioma, venous, central nervous system HSDN C2024878 Cardiovascular surgery result: dyspnea C0023869 Lithiasis HSDN C2203646 Jaundice C0745744 End stage liver disease HSDN C0518090 Frequency of pain question C0018818 Ventricular septal defects HSDN C0015672 Decreased energy C0205788 Histiocytoid hemangioma HSDN C0037763 Spasm C0016507 Acquired foot deformities HSDN C4085210 Usual severity pain C0039336 Gustatory sense HSDN C3829611 Nausea frequency C0013080 Down syndrome HSDN C0022346 Yellow skin C0037047 Sibling HSDN C1549543 Administration method - pain C0014461 Granuloma eosinophilic HSDN C1279888 Proteinuria of undiagnosed cause C0034088 Pulmonary valve insufficiency HSDN C0013911 Emaciate C0014335 Enteritis HSDN C2919142 Short stature adverse event C3537167 Trisomy 21 MalaCards C0024031 Back pain lower back C0023470 Myeloid leukemia HSDN C0917816 Deficiency mental C0432267 Tricho thiodystrophy disorder MalaCards|HPO C1069915 Vertigo C0393735 Headache disorders HSDN C0020672 Body temperature decreased C2240374 Eosinophil count raised HSDN C1557397 Adverse event associated with pain C0024958 Maxillary sinus neoplasms HSDN C2202716 Vomit containing worms C0018889 Helminthiasis UMLS C1856661 Cornea cloudy C0085859 Polyglandular type i autoimmune syndrome OrphaNet|HPO C0239376 Lower extremity pain C0002895 Anemia, sickle cell UMLS C3641755 Have constipation C0006264 Bronchial neoplasms HSDN C4085211 Pain distress question C0040028 Thrombocythemia, essential HSDN C1961131 Cough adverse event C0011881 Diabetic nephropathy HSDN C2364111 Gustatory anesthesia C0271355 Abducens nerve paralysis HSDN C0460137 Push down or depress C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0497247 Blood pressure elevation C0019101 Hemorrhagic fever with renal syndrome MalaCards C0019079 Bloody sputum C0748214 Pyriform sinus cancer squamous cell UMLS C0005874 Blush C1852146 Dermodistortive urticaria MalaCards|HPO C0007758 Cerebellar ataxia C0860603 Anxiety symptoms HSDN C1557397 Adverse event associated with pain C0031094 Periodontal pocket HSDN C1963091 Diarrhea adverse event C0042512 Ventricular outflow obstruction HSDN C0005758 Blister C1868193 Pneumothorax, primary spontaneous MalaCards C2700617 Irritation - emotion C0268548 Hyperargininemia MalaCards|HPO C4084768 Usual severity vomiting C0013870 Electroconvulsive shock HSDN C0848203 Male pelvic pain C0409354 Flexion contracture of hip HSDN C4042891 Sleep wake disorders C0079487 Helicobacter infections HSDN C4084726 Distress cough C0524910 Hepatitis c, chronic HSDN C0018681 Headache, cephalalgia C0020538 Hypertensive disease HSDN|UMLS C4084768 Usual severity vomiting C0018571 Hand injury HSDN C0023012 Delay language C0265326 Bannayan-riley-ruvalcaba syndrome MalaCards|HPO C4085211 Pain distress question C0028758 Bonding HSDN C0000731 Abdomen distention C0542428 Hypochondrogenesis HPO C3898969 Have been vomiting C0021053 Immune system diseases HSDN C0018991 Paralysis one side of body C1962979 Burn adverse event HSDN C0151825 Ostalgia C2697636 Hyperdiploid b acute lymphoblastic leukemia UMLS C0004604 Pain back C0007820 Cerebrovascular disorders HSDN C0857305 Thrombocytopenia purpura C0014457 Eosinophilia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0005417 Bile duct fistula HSDN C2024893 Cardiovascular surgery result: fatigue C0021833 Intestinal fistula HSDN C0221232 Welts C0920175 Allergic angio-oedema UMLS C1145670 Failure respiratory C2751831 Myopathy, myofibrillar, bag3-related MalaCards|HPO C0151686 Growth retardation C2750081 Diamond-blackfan anemia 9 MalaCards C0497406 Over weight C0700201 Dyssomnias HSDN C3829611 Nausea frequency C0018213 Graves disease HSDN C0518090 Frequency of pain question C0031030 Periapical periodontitis HSDN C0151786 Weakness muscle C0018133 Graft-vs-host disease HSDN C0027497 Queasy C1299919 Enteric coccidiosis HSDN C0518090 Frequency of pain question C0206180 Ki-1+ anaplastic large cell lymphoma HSDN C0036572 Convulsion C0085860 Autoimmune syndrome type ii, polyglandular MalaCards C4084776 Weight loss C0040997 Trigeminal neuralgia HSDN C0007758 Cerebellar ataxia C0024530 Malaria HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C1857777 Arrhythmogenic right ventricular dysplasia, familial, 10 HPO C0575081 Abnormal gait C0432225 Metaphyseal chondrodysplasia spahr type OrphaNet|HPO|MalaCards C0013608 Cardiac edema C1135191 Heart failure, systolic HSDN C0221150 Odynophagia C0740897 Alkalosis metabolic hypochloremic volume contraction UMLS C0023380 Lethargy C0262655 Recurrent urinary tract infection HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0038828 Arteriomesenteric duodenal ileus HSDN C0002965 Crescendo angina C0022758 Kap HSDN C1557397 Adverse event associated with pain C0024523 Malabsorption syndrome HSDN C1999266 Depression adverse event C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C0013608 Cardiac edema C0003962 Ascites HSDN C0011991 Loose stools C1863959 Hyperthyroidism, familial gestational OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0007570 Celiac disease DiseaseOntology C0030794 Pelvis pain C0206687 Carcinoma, endometrioid HSDN C0009421 Comatose C0751285 Maple syrup urine disease, thiamine responsive HPO C0023380 Lethargy C0206695 Carcinoma, neuroendocrine HSDN C4085210 Usual severity pain C0015458 Facial hemiatrophy HSDN C0344434 Atrial fibrillation ecg C1833236 Cardiomyopathy, familial hypertrophic, 6 (disorder) HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1556682 Adverse event associated with infection HSDN C0413252 Hypothermia due to exposure C0085111 Ankle injury HSDN C0037316 Not enough sleeping C0035229 Respiratory insufficiency HSDN C0041657 Consciousness loss C0344435 Ventricular fibrillation by ecg finding HSDN C0013404 Respiratory difficulty C0524620 Metabolic syndrome x HSDN C1549543 Administration method - pain C0020514 Hyperprolactinemia HSDN C0023015 Language handicap C0038220 Status epilepticus HSDN C2984057 Have nausea C0001173 Adult pyloric stenosis HSDN C0151686 Growth retardation C3553915 Methylmalonic aciduria and homocystinuria, cblj type MalaCards C2911645 Weight loss adverse event C0009373 Colonic diseases HSDN C0000727 Abdomen acute C0003811 Cardiac arrhythmia HSDN C2024893 Cardiovascular surgery result: fatigue C0950124 Papillomavirus infections HSDN C0010038 Corneal opacity disorder C1844671 Dermoids of cornea OrphaNet|MalaCards C0018784 Deafness sensorineural C0023448 Lymphoid leukemia HSDN C0035078 Failure kidney C0036421 Systemic scleroderma MalaCards C0002170 Alopecia disorders C0877265 Trichophyton infection MalaCards C0039870 Leanness C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084784 Diarrhea C0034063 Pulmonary edema HSDN C0030554 Abnormal sensation C0030783 Pellagra HSDN C0042571 Vertigo subjective C0004238 Atrial fibrillation HSDN C2919142 Short stature adverse event C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C0518090 Frequency of pain question C0018889 Helminthiasis HSDN C4084775 Usual severity weight loss C0015579 Family characteristics HSDN C0018784 Deafness sensorineural C2586211 Thrombosis of blood vessel HSDN C0349588 Stature short C2930995 Dyschromatosis universalis hereditaria MalaCards C0851578 Disorder sleep C0005891 Bodies image HSDN C1549543 Administration method - pain C0020502 Hyperparathyroidism HSDN C2984058 Have pain C0015459 Face injury HSDN C0035078 Failure kidney C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084776 Weight loss C2749484 Neuroblastoma, susceptibility to HPO C0036572 Convulsion C1864912 2-methylbutyryl-coa dehydrogenase deficiency HPO|UMLS C1963086 Confusion adverse event C0151744 Myocardial ischemia HSDN C4084784 Diarrhea C3541306 Plasmodium measurement HSDN C0007758 Cerebellar ataxia C1956097 Wolf-hirschhorn syndrome OrphaNet|HPO|MalaCards C0004134 Dyssynergia C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C0024312 Lymphocytopenia C0272167 Reticular dysgenesis MalaCards|HPO C2984058 Have pain C0020458 Hyperhidrosis disorder HSDN C0022346 Yellow skin C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C4084769 Vomiting frequency C0043528 Zoonoses HSDN C1963091 Diarrhea adverse event C0035204 Respiration disorders HSDN C0013604 Edematous C0024116 Lung diseases, fungal HSDN C3146279 Coma C0242698 Ventricular dysfunction, left HSDN C4084768 Usual severity vomiting C0003855 Arteriovenous fistula HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018051 Gonadal dysgenesis HSDN C4084727 Cough frequency C0037579 Soft tissue neoplasms HSDN C0040460 Dental pain C0040438 Ectopic tooth eruption HSDN C0036572 Convulsion C4022811 Abnormality of nervous system physiology UMLS C0232466 Feeding difficulty C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0424755 Fever symptoms C0018571 Hand injury HSDN C0035229 Respiratory function impaired C1838120 Hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities OrphaNet|MalaCards C0034155 Thrombotic thrombocytopenic purpura C0032787 Postoperative complications HSDN C0151908 Dry skin C2700553 Omenn syndrome OrphaNet|HPO|MalaCards C0085636 Light sensitivity C1851841 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 1 OrphaNet|HPO|UMLS C0005745 Blepharoptosis C0039483 Giant cell arteritis MalaCards|HPO C4085317 Diarrhea frequency C0032587 Polyradiculoneuropathy HSDN C1557397 Adverse event associated with pain C0020640 Inherited factor ii deficiency HSDN C4084724 Usual severity constipation C0520681 Central alveolar hypoventilation syndrome MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0035222 Respiratory distress syndrome, adult HSDN C0030193 Sense of pain C0033785 Pseudarthrosis HSDN C0024031 Back pain lower back C0796561 Melanoma vaccines HSDN C0037763 Spasm C1556061 Electric injuries HSDN C0004134 Dyssynergia C0004623 Bacterial infections HSDN C0013404 Respiratory difficulty C0002880 Autoimmune hemolytic anemia OrphaNet C0011991 Loose stools C0035235 Respiratory syncytial virus infections HSDN C2096293 Ent surgical result ear vertigo C0004933 Behavior modification technique HSDN C1963281 Vomiting adverse event C0029443 Osteomyelitis HSDN C0004604 Pain back C0026946 Mycoses HSDN C2242996 Tingling C0038017 Congenital spondylolisthesis HSDN C0156728 Edema or excessive weight gain in pregnancy no hypertension C0341960 Edema pregnancy UMLS C0018775 Hearing loss bilateral C0025958 Microcephaly HSDN C0242936 Center pain C0006157 Breech presentation HSDN C4084727 Cough frequency C0019621 Histiocytosis, langerhans-cell HSDN C0027497 Queasy C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN C0020615 Hypoglycemia nos C0268147 Glycogen storage disease, type ix OrphaNet C0013421 Dystonia C1690964 Cataract HSDN C0151786 Weakness muscle C0032964 Pregnancy complications, hematologic HSDN C2032396 Pelvic pain on the right C0037274 Dermatologic disorders HSDN C0020580 Decreased sensation C0015456 Facial dermatoses HSDN C0851578 Disorder sleep C0022661 Kidney failure, chronic HSDN C0454644 Delayed language development C1842676 Spinocerebellar ataxia, autosomal recessive 6 (disorder) MalaCards C0152029 Sinus congestion C0030469 Paranasal sinus diseases UMLS C0231712 Gait waddling C0795936 Eastman-bixler syndrome MalaCards|UMLS C3887638 Failure to thrive in infant C1857854 Proopiomelanocortin deficiency HPO C1963091 Diarrhea adverse event C0236733 Amphetamine-related disorders HSDN C0085636 Light sensitivity C0024437 Macular degeneration HSDN C0027796 Neuralgias C0018809 Heart neoplasm HSDN C0018681 Headache, cephalalgia C1838568 Sacral defect and anterior sacral meningocele HPO|UMLS C0018777 Deafness, conductive C0265242 Otocephaly MalaCards|HPO C4084727 Cough frequency C0003493 Aortic diseases HSDN C0015672 Decreased energy C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0030975 Disorders perception C0022698 Kinesics HSDN C0010520 Skin cyanosis C0034929 Reflex HSDN C1963281 Vomiting adverse event C0015414 Eye neoplasms HSDN C4084767 Bothered by vomiting C0004238 Atrial fibrillation HSDN C0020455 Hypergammaglobulinemia C0020639 Hypoproteinemia HSDN C4084784 Diarrhea C0334533 Arteriovenous hemangioma HSDN C0042964 Anticipatory vomiting C0009404 Colorectal neoplasms HSDN C0234132 Pyramidal sign C0022797 Adult neuronal ceroid lipofuscinosis OrphaNet|MalaCards C0243026 Generalized infection C0266209 Congenital dilatation of colon MalaCards C2032396 Pelvic pain on the right C0002871 Anemia HSDN C0413252 Hypothermia due to exposure C0268353 Cutis laxa, x-linked MalaCards C4085661 Usual severity nausea C0393735 Headache disorders HSDN C0011570 Monopolar depression C1862937 Ftdals1 MalaCards|HPO C0042798 Vision dim C2751308 Cone dystrophy 4 (disorder) MalaCards|HPO C4084784 Diarrhea C0206255 Malaria vaccine HSDN C3887784 Decreased urine output C0043398 Yellow fever, urban MalaCards C4084723 Constipation C3163620 Hypotension adverse event HSDN C0009763 Conjunctiva inflammation C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0019214 Hepatosplenomegaly C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C0518090 Frequency of pain question C1720983 Channelopathies HSDN C0036572 Convulsion C1832588 Chromosome 11p11.2 deletion syndrome OrphaNet|HPO|MalaCards C0019572 Hairiness C0086650 Mps iii d HPO C0013428 Painful urination C0041960 Ureterocele HSDN C0035078 Failure kidney C0019156 Hepatic veno-occlusive disease OrphaNet|MalaCards C0013404 Respiratory difficulty C0152171 Idiopathic pulmonary hypertension OrphaNet|HPO C0460137 Push down or depress C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0349588 Stature short C0265311 Leri pleonosteosis syndrome MalaCards C0340288 Angina stable C0011813 Dextrocardia HSDN C0424755 Fever symptoms C0018273 Growth disorders HSDN C0027066 Myoclonic jerking C0022116 Ischemia HSDN C0028738 Nystagmus C0023264 Leigh disease OrphaNet|HPO|MalaCards C0917816 Deficiency mental C1851101 Laurin-sandrow syndrome, segmental MalaCards C4084776 Weight loss C0085096 Peripheral vascular diseases HSDN C0413252 Hypothermia due to exposure C1384607 Food deprivation HSDN C0005745 Blepharoptosis C0796088 Neurofaciodigitorenal syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C0014008 Empty sella syndrome HSDN C0009421 Comatose C0027627 Neoplasm metastasis HSDN C0019825 Voice hoarseness C1334651 Choriocarcinoma of mediastinum UMLS C4084784 Diarrhea C2937358 Cerebral hemorrhage HSDN C1961131 Cough adverse event C0153414 Malignant neoplasm of middle third of esophagus MalaCards C0004134 Dyssynergia C1258104 Diffuse scleroderma HSDN C1963091 Diarrhea adverse event C0520946 Emotional hypersensitivity HSDN C4084788 Have dizziness C0039239 Sinus tachycardia HSDN C0522224 Palsied C0040053 Thrombosis HSDN C4085642 Level of joint stiffness C1706192 Sulfatidosis MalaCards C1963281 Vomiting adverse event C1623041 Breast-fed HSDN C4084769 Vomiting frequency C0030330 Panniculitis, peritoneal HSDN C0011991 Loose stools C0007932 Chagas' disease + no organ inv DiseaseOntology|MalaCards C0042024 Urine incontinence C1997362 Non-neurogenic neurogenic bladder MalaCards C4084725 Usual severity cough C0004623 Bacterial infections HSDN C0751495 Seizure focal C2751778 Generalized epilepsy with febrile seizures plus, 7 HPO|UMLS C4085862 Bothered by nausea C0003078 Aniseikonia HSDN C0030486 Extremity paralysis, lower C0017563 Gingival diseases HSDN C0221166 Paraparesis C1458155 Mammary neoplasms HSDN C3641756 Have diarrhea C0018800 Cardiomegaly HSDN C0242936 Center pain C0178282 Hernia of abdominal cavity HSDN C2984057 Have nausea C1532560 Plasmacytoma - category HSDN C0151825 Ostalgia C4038661 Pops - painful os peroneum syndrome UMLS C1291078 Epigastric discomfort C0743320 Dysphagia solid UMLS C0020580 Decreased sensation C0037933 Spinal diseases HSDN C3665492 Pigmentations C0152013 Adenocarcinoma of lung (disorder) MalaCards C0021359 Infertility C0221406 Pituitary-dependent cushing's disease OrphaNet|HPO C0033377 Caudal displacement C1862263 Bpes without ovarian failure HPO C0424755 Fever symptoms C0009376 Colonic polyps HSDN C0851578 Disorder sleep C1956346 Coronary artery disease HSDN C4084725 Usual severity cough C0263666 Dermatomyositis, childhood type MalaCards C0036572 Convulsion C0036690 Septicemia HSDN C0349588 Stature short C2713321 Alpha-l-iduronidase deficiency OrphaNet C2926613 Chest pain:finding:point in time:^patient:ordinal C0040136 Thyroid neoplasm HSDN C0040822 D tremors C0997768 Glaucoma HSDN C0242936 Center pain C0014866 Esophageal stenosis HSDN C0009806 Constipate C0423742 Intercourse pain HSDN C0018524 Hallucinate C1833473 Dermoid cysts, familial frontonasal MalaCards C1069915 Vertigo C0524812 Intracranial hypotension HSDN C2237041 Shox gene with short stature C2675229 Ciliary dyskinesia, primary, 11 MalaCards|HPO C2237041 Shox gene with short stature C1837830 Ulnar-fibular ray defect and brachydactyly OrphaNet|MalaCards C1557397 Adverse event associated with pain C0017400 Behavioral genetics HSDN C0151786 Weakness muscle C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0035066 Renal artery obstruction HSDN C0037384 Snore C0011849 Diabetes mellitus HSDN C1557397 Adverse event associated with pain C0027645 Neoplasm seeding HSDN C0018772 Deafness C0002994 Angioedema HSDN C0009806 Constipate C0268322 Chester-type porphyria HPO C0018991 Paralysis one side of body C0038874 Supratentorial neoplasms HSDN C0018772 Deafness C0268363 Osteogenesis imperfecta type iv (disorder) MalaCards|HPO C4085210 Usual severity pain C0398623 Thrombophilia HSDN C0344315 Mood depressed C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C0040822 D tremors C0032914 Pre-eclampsia HSDN C0427008 Stiffness C4225273 Spondyloepiphyseal dysplasia, stanescu type UMLS C0878773 Bladder hyperactive C3554520 Ufs2 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0043528 Zoonoses HSDN C0018808 Murmur C0003493 Aortic diseases HSDN C0018784 Deafness sensorineural C0014457 Eosinophilia HSDN C1579931 Depressed - symptom C1868596 Atypical parkinson disease HPO C0034124 Pupillary disorder C0011854 Diabetes mellitus, insulin-dependent HSDN C0152116 Torticollis spasmodic C1709838 Rare non-neoplastic disorder UMLS C4084724 Usual severity constipation C1136249 Mental retardation, x-linked HSDN C1963184 Nystagmus adverse event C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C4084769 Vomiting frequency C0035400 Reyes syndrome HSDN C0040822 D tremors C0042487 Venous thrombosis HSDN C2237041 Shox gene with short stature C1856113 Mowat-wilson syndrome OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0810269 Headache other UMLS C3539022 Pelvic pain decreasing in severity C0007621 Neoplastic cell transformation HSDN C0013421 Dystonia C0268273 Gangliosidosis, generalized gm1, type 3 MalaCards|HPO C0036572 Convulsion C0278187 Akinetic seizure without atonia UMLS C0027066 Myoclonic jerking C0040517 Gilles de la tourette syndrome HSDN C0002962 Angina C0041755 Adverse reaction to drug HSDN C4084788 Have dizziness C0004153 Atherosclerosis HSDN C0018784 Deafness sensorineural C0031154 Peritonitis HSDN C4042891 Sleep wake disorders C0018621 Hay fever HSDN C1963091 Diarrhea adverse event C0032343 Poisoning HSDN C4084776 Weight loss C1334818 Multicystic mesothelioma of peritoneum MalaCards C3539020 Pelvic pain decreasing in frequency C0021359 Infertility HSDN C0009676 Confusion state C1963138 Hypertension adverse event HSDN C0000737 Abdomen pain C0003838 Arterial occlusive diseases HSDN C0014724 Burping C0021831 Intestinal diseases HSDN C0038002 Spleen enlargement C0398367 Histiocytic necrotizing lymphadenitis MalaCards C1557397 Adverse event associated with pain C0043254 Injuries penetrating HSDN C0034150 Skin purpura C0344434 Atrial fibrillation ecg HSDN C4050613 Anxiety C0013384 Dyskinetic syndrome MalaCards C0460137 Push down or depress C3149705 Parkinson disease 1, autosomal dominant lewy body HPO C4085548 Usual severity dizziness C1552262 Nurse practitioner - family HSDN C0039870 Leanness C0162425 Intent HSDN C4085210 Usual severity pain C1963107 Euphoria adverse event HSDN C4085317 Diarrhea frequency C0027868 Neuromuscular diseases HSDN C0013428 Painful urination C1511203 Bladder tubulo-cystic clear cell adenocarcinoma UMLS C0037771 Paraparesis spastic C0751587 Cadasil syndrome HSDN C0004134 Dyssynergia C1864669 Neuronal ceroid lipofuscinosis due to cathepsin d deficiency MalaCards|HPO|UMLS C1962957 Flushing adverse event C0014859 Esophageal neoplasms HSDN C0040822 D tremors C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C0037763 Spasm C1319018 Asthmatic bronchitis UMLS C0020538 Hbp C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0231218 Malaise generalized C1336223 Stage iiib carcinoma of liver cells UMLS C2024893 Cardiovascular surgery result: fatigue C0015397 Disorder of eye HSDN C2187990 Unable to perform sex C0007795 Diffuse cerebral sclerosis of schilder MalaCards C3146279 Coma C0003615 Appendicitis HSDN C1963249 Tinnitus adverse event C1962958 Hematoma adverse event HSDN C2073625 X-ray of chest: pleural effusion C0024215 Lymphangiectasis, intestinal MalaCards C3641756 Have diarrhea C0020413 Hymenolepiasis DiseaseOntology|HSDN C1963281 Vomiting adverse event C0018824 Heart valve disease HSDN C4085317 Diarrhea frequency C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C4085211 Pain distress question C0015300 Exophthalmos HSDN C3829611 Nausea frequency C0524909 Hepatitis b, chronic MalaCards|HSDN C0024032 Birth weight subnormal C0751038 Cockayne syndrome, type ii HPO C3274924 Have been coughing C0005940 Bone diseases HSDN C0043094 Weight gain C0026636 Mouth diseases HSDN C0857305 Thrombocytopenia purpura C0035229 Respiratory insufficiency HSDN C0750937 Appendicular ataxia C4014261 Spinocerebellar ataxia, autosomal recessive 16 MalaCards C1963087 Constipation adverse event C0021364 Male infertility HSDN C0026838 Spasticity muscle C0035309 Retinal diseases HSDN C0036572 Convulsion C0600091 Identifiers HSDN C1963063 Anorexia adverse event C0041296 Tuberculosis HSDN C1963281 Vomiting adverse event C0270726 Alexander disease HSDN C2029884 Hearing loss by exam C0036974 Shock HSDN C0000727 Abdomen acute C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4084723 Constipation C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C0151786 Weakness muscle C1269683 Major depressive disorder HSDN C2203646 Jaundice C0022423 Judgement HSDN C4085661 Usual severity nausea C2911643 Encounter due to family history of osteoporosis HSDN C1549543 Administration method - pain C0029139 Optical illusion HSDN C0007166 Cardiac output decreased C3812171 Bradycardia by ecg finding HSDN C0018775 Hearing loss bilateral C0453996 Tobacco smoking HSDN C2984058 Have pain C0917875 Esophageal diverticulosis HSDN C1961131 Cough adverse event C0549143 Pulmonary renal syndrome MalaCards C0040485 Wryneck C0004106 Astigmatism HSDN C0427055 Face weakness C2931811 Chromosome 18, trisomy 18p MalaCards C0023222 Lower extremity pain musculoskeletal C0231767 Achillodynia UMLS C2984058 Have pain C0043324 Juvenile xanthogranuloma HSDN C0033774 Skin pruritus C1546847 Entity name part type - family HSDN C4084774 Have weight loss C0010678 Cysticercosis HSDN C0009792 Consciousness disorder C0019624 Histiocytosis, non-langerhans-cell HSDN C3815497 Cough C0019557 Hip fx HSDN C0026858 Musculoskeletal pain C0022104 Irritable bowel syndrome HSDN C4084767 Bothered by vomiting C0037313 Sleep HSDN C4085211 Pain distress question C0033680 Protein-losing enteropathies HSDN C0015970 Fever unknown origin C0018801 Heart failure HSDN C0042798 Vision dim C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C0003467 Angst C0010481 Cushing syndrome OrphaNet|HPO|MalaCards C1527344 Dysphonia C2240378 Cleft palate on exam HSDN C2984057 Have nausea C0039483 Giant cell arteritis HSDN C0036572 Convulsion C0265268 Adams oliver syndrome MalaCards|HPO|UMLS C4084767 Bothered by vomiting C0023283 Leishmaniasis, cutaneous HSDN C4084784 Diarrhea C0003125 Anorexia nervosa HSDN C4085661 Usual severity nausea C0019693 Hiv infections HSDN C4084774 Have weight loss C0005940 Bone diseases HSDN C0042798 Vision dim C0205710 Alpers syndrome (disorder) MalaCards C4085317 Diarrhea frequency C0035229 Respiratory insufficiency HSDN C4084773 Bothered by weight gain C0302280 Adrenogenital syndrome HSDN C2984058 Have pain C0003872 Arthritis, psoriatic HSDN C0085128 Cardiac output elevated C1145628 Autonomic nervous system disorders HSDN C0026838 Spasticity muscle C1835671 Axonal neuropathy with palmoplantar keratoderma MalaCards C2362324 Pediatric obesity C0020655 Hypothalamic diseases HSDN C4084725 Usual severity cough C1306577 Dies patient HSDN C0011206 Delirium acute C0010346 Crohn disease HSDN C0917816 Deficiency mental C1859844 Leber congenital amaurosis, type ii (disorder) MalaCards|HPO C0023012 Delay language C0220704 Shprintzen syndrome MalaCards C0036572 Convulsion C1510460 Orofaciodigital syndrome i OrphaNet|UMLS|HPO|MalaCards C0151311 Cranial nerve palsy C1304205 Neutrophilic urticaria MalaCards C0023380 Lethargy C0268569 Intermittent maple syrup urine disease HPO C2024893 Cardiovascular surgery result: fatigue C0037274 Dermatologic disorders HSDN C1069915 Vertigo C0001721 Emotional affect HSDN C2984057 Have nausea C1704326 Role - roleclass HSDN C0020673 Hypothermia (central) (local) C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C2237041 Shox gene with short stature C1845892 Hprt deficiency, neurologic variant HPO C0036572 Convulsion C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C0011206 Delirium acute C0006895 Capgras syndrome HSDN C4084802 Usual severity diarrhea C0032310 Pneumonia, viral HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0005974 Bone resorption HSDN C1962972 Proteinuria adverse event C0030521 Parathyroid neoplasms HSDN C0018772 Deafness C1852718 Branchiootic syndrome 2 MalaCards C0518090 Frequency of pain question C0016045 Fibroma HSDN C0010038 Corneal opacity disorder C0751544 Tangier disease neuropathy MalaCards C0030200 Intractable pain C0025202 Melanoma HSDN C0030552 Paralysis partial C0751850 Heavy metal poisoning, nervous system HSDN C0522224 Palsied C0007570 Celiac disease HSDN C3641755 Have constipation C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C0004604 Pain back C0024232 Lymphatic metastasis HSDN C0033774 Skin pruritus C0011615 Dermatitis, atopic UMLS C2096293 Ent surgical result ear vertigo C0034530 Injury radiation HSDN C0042571 Vertigo subjective C0035126 Reperfusion injury HSDN C0022346 Yellow skin C1333307 Adenocarcinoma of distal 1/3 of common bile duct UMLS C0024031 Back pain lower back C0236736 Cocaine-related disorders HSDN C0727671 Red cross toothache drops C0040445 Tooth mobility HSDN C1963281 Vomiting adverse event C4085311 Depression - recess HSDN C4085317 Diarrhea frequency C0086649 Mps iii c HPO C0042940 Disorder of voice C0027643 Neoplasm recurrence, local HSDN C0026884 Muteness C0152179 Disease vagus nerve HSDN C4085548 Usual severity dizziness C2984299 Asthma pathway HSDN C0015672 Decreased energy C0151744 Myocardial ischemia HSDN C2203646 Jaundice C0854795 Resectable hepatic malignant neoplasm MalaCards C3463815 Feel fatigue C0027127 Myotonia congenita HSDN C1549543 Administration method - pain C0752308 Hypoxia-ischemia, brain HSDN C0375212 Spastic hemiplegia, affecting nondominant side C0154694 Spastic hemiplegia UMLS C0012833 Dizzy C0750929 Arnold-chiari malformation, type i MalaCards|UMLS C0036572 Convulsion C4015420 Epilepsy, progressive myoclonic 7 MalaCards C1963170 Hypothermia adverse event C0038187 Starvation HSDN C1963091 Diarrhea adverse event C0023176 Lead poisoning MalaCards|HSDN C0023015 Language handicap C0003646 Aptitude HSDN C1145670 Failure respiratory C3554235 Joubert syndrome 20 MalaCards C0027497 Queasy C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084726 Distress cough C0342443 Adrenal cushing's syndrome HSDN C4084774 Have weight loss C0340629 Aortic aneurysm without mention of rupture nos HSDN C4085211 Pain distress question C0001824 Agranulocytosis HSDN C1963091 Diarrhea adverse event C0036202 Sarcoidosis HSDN C4084723 Constipation C0342257 Complications of diabetes mellitus HSDN C0151825 Ostalgia C0263628 Tumoral calcinosis OrphaNet|MalaCards C0015230 Exanthem C0406240 Light-sensitive atopic eczema UMLS C4085222 Nausea C0001430 Adenoma HSDN C4084725 Usual severity cough C0007621 Neoplastic cell transformation HSDN C1549543 Administration method - pain C1636667 Disorder characterized by eosinophilia HSDN C0025287 Meningitis-like C0276226 Herpes encephalitis HSDN C0027796 Neuralgias C0162871 Aortic aneurysm, abdominal HSDN C4084775 Usual severity weight loss C0018802 Congestive heart failure HSDN C1549543 Administration method - pain C0022568 Keratitis HSDN C4084784 Diarrhea C3149237 Men1 somatic mutations HPO C1145670 Failure respiratory C0265241 Franceschetti-klein syndrome MalaCards|HPO C0424755 Fever symptoms C0001969 Alcoholic intoxication HSDN C0010200 Cough symptom C0039685 Tetralogy of fallot HSDN C0015230 Exanthem C1304205 Neutrophilic urticaria MalaCards C4084802 Usual severity diarrhea C0037397 Behavior social HSDN C2984058 Have pain C0017417 Genital neoplasms, male HSDN C0085636 Light sensitivity C0268138 Xeroderma pigmentosum, complementation group d HPO|UMLS C0020672 Body temperature decreased C0268353 Cutis laxa, x-linked MalaCards C0015230 Exanthem C4047486 Herpes zoster of skin of neck UMLS C3887638 Failure to thrive in infant C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C1963063 Anorexia adverse event C0024899 Mastocytosis MalaCards C0851578 Disorder sleep C0021361 Female infertility HSDN C0398650 Idiopathic thrombocytopenia purpura C0019066 Nontraumatic hemoperitoneum HSDN C1384666 Decreased hearing C0041296 Tuberculosis HSDN C0009398 Color vision defects C1419610 Rp23 gene MalaCards|HPO C4085211 Pain distress question C2984330 Chagas disease pathway HSDN C0011991 Loose stools C0473132 Diarrhea toddler UMLS C0178417 Anhedonia C0038436 Post-traumatic stress disorder HSDN C0011991 Loose stools C0024530 Malaria HSDN C0016382 Cutaneous vascular engorgement C2931735 Epidermolytic palmoplantar keratoderma vorner type OrphaNet|HPO|MalaCards C1963252 Tremor adverse event C0007117 Basal cell carcinoma HSDN C4084802 Usual severity diarrhea C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0036572 Convulsion C0795970 Craniofacial digital genital anomalies MalaCards C0011991 Loose stools C0042338 Herpesvirus 3, human HSDN C3541349 Syncope C0018817 Atrial septal defects HSDN C3887873 Hearing loss C1527231 Adrenomyeloneuropathy MalaCards C0015672 Decreased energy C0241158 Cicatrix skin HSDN C0030794 Pelvis pain C0010356 Cross infection HSDN C0577567 Mass of urogenital structure C0042076 Urologic neoplasms UMLS C0027796 Neuralgias C0017409 Herpes zoster oticus UMLS C0018926 Emesis bloody C0030297 Pancreatic neoplasm HSDN C0234376 Tremor action C1859093 Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism MalaCards|HPO|UMLS C4085317 Diarrhea frequency C0002874 Aplastic anemia HSDN C0917816 Deficiency mental C1846389 Cortical dysplasia of taylor with balloon cells HPO C0027796 Neuralgias C3714514 Infection HSDN C0011991 Loose stools C0151718 Hypocholesterolemia UMLS C0917816 Deficiency mental C1853925 Spondyloocular syndrome, autosomal recessive MalaCards|HPO C3641756 Have diarrhea C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C1963281 Vomiting adverse event C1269683 Major depressive disorder HSDN C2237041 Shox gene with short stature C2931597 Macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance MalaCards C0086439 Activity decreased C0035410 Rhabdomyolysis HSDN C0018772 Deafness C3165526 Congenital iodine deficiency syndrome MalaCards C0848203 Male pelvic pain C0520946 Emotional hypersensitivity HSDN C0024031 Back pain lower back C0004442 Avoidance learning HSDN C0026838 Spasticity muscle C0040128 Thyroid diseases HSDN C0020450 Hyperemesis gravidarum C0013363 Dysautonomia HSDN C0043094 Weight gain C0015652 Fascioliasis HSDN C3463815 Feel fatigue C0002880 Autoimmune hemolytic anemia OrphaNet C0004604 Pain back C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0009421 Comatose C0026636 Mouth diseases HSDN C0004134 Dyssynergia C0349604 Intracranial meningioma MalaCards C0003550 Broca aphasia C0024149 Luria-nebraska neuropsychological battery HSDN C0750426 Wbc elevated C1834582 Myeloproliferative syndrome, transient MalaCards C0000737 Abdomen pain C0242996 Learning, maze HSDN C0020578 Hyperventilate C0034088 Pulmonary valve insufficiency HSDN C0016382 Cutaneous vascular engorgement C0342861 Uroporphyrinogen decarboxylase deficiency MalaCards C0518090 Frequency of pain question C0001824 Agranulocytosis HSDN C0751265 Learning disability C0012236 Digeorge syndrome MalaCards C0018772 Deafness C0007350 Cat disease HSDN C0518090 Frequency of pain question C0423772 Cutaneous fistula HSDN C0020615 Hypoglycemia nos C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards|HPO C0004134 Dyssynergia C0024003 Lordosis HSDN C0041657 Consciousness loss C0007781 Intracranial embolism and thrombosis HSDN C0015676 Mental fatigue C1968835 Egot gene HSDN C0009806 Constipate C2586211 Thrombosis of blood vessel HSDN C0002170 Alopecia disorders C0342286 Woodhouse sakati syndrome OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C3151857 Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism MalaCards C0033774 Skin pruritus C0031511 Pheochromocytoma HSDN C0018524 Hallucinate C0085541 Epilepsy, frontal lobe HSDN C4085210 Usual severity pain C0017086 Gangrene HSDN C0018808 Murmur C0026691 Mucocutaneous lymph node syndrome HSDN C0850758 Pain pelvic C0010068 Coronary heart disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0014013 Empyema, pleural DiseaseOntology|HSDN C0522224 Palsied C0085094 Head injury closed HSDN C0007758 Cerebellar ataxia C4014621 Eiee25 MalaCards C0018681 Headache, cephalalgia C0027643 Neoplasm recurrence, local HSDN C3641756 Have diarrhea C0007682 Cns disorder HSDN C4084776 Weight loss C0473572 Diffuse palmoplantar keratoderma with esophageal cancer MalaCards C0019521 Hiccoughs C0025060 Mediastinal cyst HSDN C4084897 Sleep disturbance subordinate domain C0028064 Niemann-pick diseases MalaCards C1279888 Proteinuria of undiagnosed cause C0342750 Glycogen storage disease type id MalaCards|HPO C4084775 Usual severity weight loss C0007095 Carcinoid tumor HSDN C0042798 Vision dim C1852020 Malattia leventinese HPO C4084724 Usual severity constipation C0004275 Attitude health HSDN C0018681 Headache, cephalalgia C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C0018784 Deafness sensorineural C1275808 Congenital central hypoventilation MalaCards C0004941 Behavioral symptoms C0242526 Gonadal dysgenesis, 45,x OrphaNet C0015300 Ocular proptosis C0265308 Baller-gerold syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0015630 Fantasies HSDN C0857223 Esophagus sore C0014868 Esophagitis UMLS C0037317 Sleep disturbance C0270726 Alexander disease OrphaNet|MalaCards C0026838 Spasticity muscle C0034530 Injury radiation HSDN C0011991 Loose stools C4084839 Scabies HSDN C0013404 Respiratory difficulty C1963067 Atrial fibrillation adverse event HSDN C3665347 Vision impaired C0398621 Hypoplasminogenemia MalaCards C1963249 Tinnitus adverse event C1690964 Cataract HSDN C0015672 Decreased energy C0011848 Diabetes insipidus HSDN C4085211 Pain distress question C0014179 Endometritis HSDN C0018989 Paresis of one side of body C1846386 Focal cortical dysplasia of taylor, type iia HPO C0426579 Anorexia symptom C0030528 Paratyphoid fever DiseaseOntology|MalaCards C0010038 Corneal opacity disorder C1857572 Corneal dystrophy and perceptive deafness OrphaNet|HPO C0557874 Global developmental delay C3280314 Combined malonic and methylmalonic aciduria MalaCards C0026825 Flaccidity muscle C1306794 Wound botulism MalaCards C0030486 Extremity paralysis, lower C1000483 Genus anemia HSDN C1963087 Constipation adverse event C0038358 Gastric ulcer HSDN C0020580 Decreased sensation C1261470 Congenital meningocele HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C3887638 Failure to thrive in infant C3809233 Noonan syndrome 8 MalaCards C0013604 Edematous C0027831 Neurofibromatosis 1 HSDN C0413252 Hypothermia due to exposure C0024117 Chronic obstructive airway disease HSDN C0152459 Striae C0020428 Hyperaldosteronism MalaCards C0011991 Loose stools C0699744 Infection of ear HSDN C0010038 Corneal opacity disorder C1860224 Ablepharon-macrostomia syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0027868 Neuromuscular diseases HSDN C0026821 Cramp C0040409 Tongue diseases HSDN C0040485 Wryneck C0042797 Monocular vision HSDN C2237041 Shox gene with short stature C0268312 Progressive intrahepatic cholestasis (disorder) OrphaNet C0456073 Neonatal facial petechiae C1290857 Disorder of face UMLS C0042571 Vertigo subjective C0456750 Nystagmus, positional, central type UMLS C4084766 Vomiting C0038000 Spleen rupture HSDN C0042798 Vision dim C4014538 Helsmoortel-van der aa syndrome MalaCards C0152169 Colic renal C1956418 Torsion abnormality HSDN C0234132 Pyramidal sign C0086431 Hurler-scheie syndrome OrphaNet|HPO C0242936 Center pain C0008065 Childhood behavior HSDN C4084775 Usual severity weight loss C0019154 Hepatic vein thrombosis MalaCards|HPO C0575081 Abnormal gait C1838280 Epiphyseal dysplasia, multiple, 1 OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C0009450 Disease caused by microorganism HSDN C3641755 Have constipation C0018674 Head trauma HSDN C0042928 Paralysis vocal cord C1546747 Specimen source codes - polyps HSDN C0424755 Fever symptoms C0030283 Pancreatic cyst HSDN C1963065 Apnea adverse event C0032787 Postoperative complications HSDN C0017181 Gastrointestinal bleed C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C0349588 Stature short C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C0016053 Fibromyalgia HSDN C2096293 Ent surgical result ear vertigo C0035078 Kidney failure HSDN C3887638 Failure to thrive in infant C0206733 Strawberry nevus of skin HSDN C1963281 Vomiting adverse event C1864996 Enteric neuropathy, familial MalaCards C0042024 Urine incontinence C0021783 Internal external locus of control HSDN C0080274 Retention urinary C0011989 Camurati-engelmann syndrome MalaCards|HPO C1962972 Proteinuria adverse event C0019621 Histiocytosis, langerhans-cell HSDN C3274924 Have been coughing C0025521 Inborn errors of metabolism HSDN C0018784 Deafness sensorineural C3463824 Myelodysplastic syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032002 Pituitary diseases HSDN C1963065 Apnea adverse event C0038186 Reflex, startle HSDN C0013604 Edematous C0035127 Cumulative trauma disorders HSDN C0034933 Abnormal reflexes C2937358 Cerebral hemorrhage HSDN C2911645 Weight loss adverse event C0220847 C hepatitis virus HSDN C0013604 Edematous C0043325 Xanthomatosis HSDN C3463815 Feel fatigue C0001430 Adenoma HSDN C4085862 Bothered by nausea C1999266 Depression adverse event HSDN C0270844 Convulsions tonic C0393706 Early infantile epileptic encephalopathy with suppression bursts MalaCards C0015672 Decreased energy C0043352 Xerostomia HSDN C0151786 Weakness muscle C1961100 Erectile dysfunction adverse event HSDN C0518090 Frequency of pain question C2931642 Benign symmetrical lipomatosis HSDN C0030193 Sense of pain C0033054 Prenatal exposure delayed effects HSDN C0085636 Light sensitivity C1857618 Achromatopsia 2 MalaCards|HPO|UMLS C3641755 Have constipation C1275808 Congenital central hypoventilation MalaCards|HPO C0240991 Sensory ataxia C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO|UMLS C0004134 Dyssynergia C0003803 Arnold chiari malformation MalaCards|HSDN C0162298 Stiffness joints C0029420 Osteochondritis MalaCards C0268988 Itch penis C1302834 Disorder of skin of trunk UMLS C0042024 Urine incontinence C0013274 Patent ductus arteriosus HSDN C1963071 Back pain adverse event C0034088 Pulmonary valve insufficiency HSDN C1557397 Adverse event associated with pain C0018805 Heart injuries HSDN C4084725 Usual severity cough C2609059 Antisynthetase syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0036494 Mal de mer UMLS C1963164 Lymphopenia adverse event C3809383 Immunodeficiency 8 MalaCards C2984058 Have pain C0040896 Trichinellosis HSDN C0010200 Cough symptom C0019196 Hepatitis c HSDN C0015672 Decreased energy C0006114 Cerebral edema HSDN C1963065 Apnea adverse event C1865295 Auriculo-condylar syndrome MalaCards|HPO C4084723 Constipation C0220847 C hepatitis virus HSDN C0030193 Sense of pain C0025299 Meningocele HSDN C0033774 Skin pruritus C2987483 Stage 0 vulvar cancer UMLS C0030554 Abnormal sensation C3150972 Neuropathy, hereditary sensory, type id MalaCards|HPO C0018777 Deafness, conductive C0265554 Ectrodactyly MalaCards C1549543 Administration method - pain C0023348 Leprosy, lepromatous HSDN C1384666 Decreased hearing C1846056 Abidi x-linked mental retardation syndrome OrphaNet|MalaCards C0002170 Alopecia disorders C3494489 Autoimmune polyendocrinopathy syndrome, type 1 HPO C4085317 Diarrhea frequency C2936797 Acid cholesteryl ester hydrolase deficiency, type 2 OrphaNet C0151686 Growth retardation C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO C0009676 Confusion state C0030783 Pellagra HSDN C0009806 Constipate C0238198 Gastrointestinal stromal tumors OrphaNet|HPO|MalaCards C0013421 Dystonia C2750442 Hypermanganesemia with dystonia polycythemia and cirrhosis HPO C3463815 Feel fatigue C0027819 Neuroblastoma HSDN C0023014 Developmental disorder language C0040369 Economy token HSDN C0013604 Edematous C1850055 Peho syndrome MalaCards|HPO C0036572 Convulsion C4041080 Neurocognitive disorders HSDN C0009024 Clonus C2676466 Pontocerebellar hypoplasia type 2b HPO|UMLS C0042571 Vertigo subjective C1258104 Diffuse scleroderma HSDN C2911647 Weight gain adverse event C0003811 Cardiac arrhythmia HSDN C1999266 Depression adverse event C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C0019572 Hairiness C4012050 Hennekam lymphangiectasia-lymphedema syndrome 1 MalaCards C3714552 Strength decreased C2939420 Metastatic neoplasm UMLS C0018784 Deafness sensorineural C0031149 Peritoneal neoplasms HSDN C4042891 Sleep wake disorders C0262584 Carcinoma, small cell HSDN C0026838 Spasticity muscle C0023374 Lesch-nyhan syndrome OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0018789 Cardiac aneurysm HSDN C0020580 Decreased sensation C0003873 Rheumatoid arthritis HSDN C0917816 Deficiency mental C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0454644 Delayed language development C2931338 Chromosome 3, monosomy 3q13 MalaCards C0497247 Blood pressure elevation C0220679 Ehlers-danlos syndrome, autosomal dominant, type unspecified OrphaNet C0037284 Skin lesion C0043388 Bouba DiseaseOntology|MalaCards C0851578 Disorder sleep C0016542 Foreign body HSDN C0150045 Urinary incontinence urge C0034183 Pyelitis unspecified HSDN C0030193 Sense of pain C0032461 Polycythemia HSDN C1963071 Back pain adverse event C0270611 Brain damage HSDN C0003962 Ascites C0086768 Pancreatic cholera MalaCards C3539893 Pelvic pain occurs with intercourse C0600041 Infective cystitis HSDN C2024893 Cardiovascular surgery result: fatigue C0003507 Aortic valve stenosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017510 Gestures HSDN C0004941 Behavioral symptoms C3146244 Alcohol related birth defect OrphaNet|MalaCards C0413252 Hypothermia due to exposure C1457883 Aggressive reaction HSDN C0018808 Murmur C3714514 Infection HSDN C0151786 Weakness muscle C0270932 Neuropathy paraneoplastic HSDN C0085636 Light sensitivity C1832976 Cone-rod dystrophy 5 MalaCards|HPO C0011206 Delirium acute C2239176 Liver carcinoma HSDN C0034933 Abnormal reflexes C0009324 Ulcerative colitis HSDN C2315100 Pediatric failure to thrive C3711125 Mitochondrial dna depletion syndrome 8a MalaCards C0000737 Abdomen pain C0524851 Neurodegenerative disorders HSDN C0027497 Queasy C0008066 Child behavior disorders HSDN C0027497 Queasy C0018188 Granuloma HSDN C3898969 Have been vomiting C0206715 Neoplasms, neuroepithelial HSDN C3274924 Have been coughing C0020437 Hypercalcemia HSDN C1549543 Administration method - pain C0010633 Cystadenoma HSDN C0030193 Sense of pain C1879737 Aromatherapy and essential oils HSDN C0151889 Reflexes tendon increased C0023806 Lipomucopolysaccharidosis HPO C0020615 Hypoglycemia nos C1850406 Navajo neurohepatopathy MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0024141 Lupus erythematosus, systemic HSDN C3887873 Hearing loss C0023269 Leiomyosarcoma HSDN C0042024 Urine incontinence C0221392 Vaginitis atropic HSDN C0009421 Comatose C0013295 Duodenal ulcer HSDN C0270948 Neurogenic muscular atrophy C0017923 Glycogen storage disease type iv MalaCards|HPO C0042928 Paralysis vocal cord C0751792 Trauma, nervous system HSDN C0008031 Pain chest C0041188 Pyomyositis, tropical HSDN C0037316 Not enough sleeping C0018790 Cardiac arrest HSDN C1963091 Diarrhea adverse event C0221204 Lytic lesion HSDN C2029884 Hearing loss by exam C0032019 Pituitary neoplasms HSDN C4049644 Depression C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C4084802 Usual severity diarrhea C0043349 Xerophthalmia HSDN C0020672 Body temperature decreased C0019069 Hemophilia a HSDN C0036572 Convulsion C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards|HPO|UMLS C4085210 Usual severity pain C0038017 Congenital spondylolisthesis HSDN C0035232 Diaphragmatic paralysis C0221056 Adult type dermatomyositis HSDN C0011991 Loose stools C0342288 Insulin-dependent diabetes mellitus secretory diarrhea syndrome MalaCards|HPO C2984057 Have nausea C0038454 Cerebrovascular accident HSDN C1963252 Tremor adverse event C0751254 Creutzfeldt-jakob disease, familial MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0001175 Acquired immunodeficiency syndrome HSDN C2242996 Tingling C0042769 Virus diseases HSDN C3887638 Failure to thrive in infant C1840437 Isolated hyperchlorhidrosis HPO C0018784 Deafness sensorineural C0011854 Diabetes mellitus, insulin-dependent HSDN C0011991 Loose stools C0030312 Pancytopenia UMLS C4084774 Have weight loss C0027947 Neutropenia HSDN C0018991 Paralysis one side of body C0036421 Systemic scleroderma HSDN C0237326 Defecation pain C1855923 Hyperphosphatasia with mental retardation MalaCards|HPO C4084769 Vomiting frequency C0020443 Hypercholesterolemia HSDN C3898969 Have been vomiting C0028738 Nystagmus HSDN C1963065 Apnea adverse event C0033817 Pseudomonas infections HSDN C4085661 Usual severity nausea C0043352 Xerostomia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1547046 Kind of quantity - taste HSDN C0917816 Deficiency mental C2752048 Gabrielli syndrome MalaCards C0007815 Cerebrospinal fluid rhinorrhoea C0022661 Kidney failure, chronic HSDN C0020305 Fetal edema C1135956 Maternal fetal relations HSDN C4085210 Usual severity pain C1963119 Stomach ulcer adverse event HSDN C0231528 Muscle pain generalized C0242188 Spider bites HSDN C0349588 Stature short C1853100 Cerebrooculofacioskeletal syndrome 4 MalaCards|HPO C0349588 Stature short C1845861 Mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait OrphaNet|HPO C0030552 Paralysis partial C0393799 Miller fisher syndrome HSDN C0030554 Abnormal sensation C0037299 Skin ulcer HSDN C0241137 Skin pallor C1832592 Hernandez fragoso syndrome OrphaNet|MalaCards C4085661 Usual severity nausea C0007194 Hypertrophic cardiomyopathy HSDN C4084768 Usual severity vomiting C0001175 Acquired immunodeficiency syndrome HSDN C0031911 Pigment deposition C0015414 Eye neoplasms MalaCards C0162292 Extraocular palsy C1834673 Facioscapulohumeral muscular dystrophy 1a MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0085605 Liver failure HSDN C0162298 Stiffness joints C0085435 Arthritis, reactive OrphaNet|MalaCards C1557397 Adverse event associated with pain C0006060 Boutonneuse fever HSDN C0011991 Loose stools C0275983 Bovine coronoviral diarrhea UMLS C0018681 Headache, cephalalgia C0035302 Retinal artery occlusion HSDN C0917816 Deficiency mental C1306862 Atrophy blanche MalaCards C2237041 Shox gene with short stature C1850627 Keipert syndrome MalaCards C4084723 Constipation C0020255 Hydrocephalus HSDN C0002170 Alopecia disorders C1956390 Cranial arteritis MalaCards C0015468 Face pain C2239176 Liver carcinoma HSDN C0022346 Yellow skin C2931878 Familial primary biliary cirrhosis MalaCards C0011991 Loose stools C0162703 Pain sensitivity HSDN C0018808 Murmur C2984299 Asthma pathway HSDN C0242936 Center pain C0032326 Pneumothorax HSDN C4084776 Weight loss C0033871 Psychiatric status rating scales HSDN C3541349 Syncope C0002792 Anaphylaxis HSDN C0235153 Sensory hallucination C0022336 Creutzfeldt-jakob disease MalaCards|HPO C4084724 Usual severity constipation C0027746 Nerve degeneration HSDN C0013604 Edematous C0853697 Neutrophil count decreased HSDN C1557397 Adverse event associated with pain C0025500 Mesothelioma HSDN C2096293 Ent surgical result ear vertigo C0003708 Arachnitis HSDN C1963065 Apnea adverse event C0010340 Critical illness HSDN C1961131 Cough adverse event C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C0241137 Skin pallor C0020305 Hydrops fetalis MalaCards C0042571 Vertigo subjective C0007137 Squamous cell carcinoma HSDN C0009792 Consciousness disorder C0035204 Respiration disorders HSDN C0851578 Disorder sleep C0795841 Jacobsen distal 11q deletion syndrome HSDN C0020673 Hypothermia (central) (local) C1578691 Congenital myxedema MalaCards C4084784 Diarrhea C0003492 Aortic coarctation HSDN C0424755 Fever symptoms C0024301 Lymphoma, follicular OrphaNet|HPO|MalaCards C0007166 Cardiac output decreased C0003486 Aortic aneurysm HSDN C0518090 Frequency of pain question C0016558 Forensic psychiatri HSDN C0424755 Fever symptoms C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0030193 Sense of pain C1961100 Erectile dysfunction adverse event HSDN C0042025 Urinary incontinence stress C0006663 Calcinosis HSDN C0022107 Fussiness C0342646 Vitamin d-dependent rickets, type 2a HPO C0011991 Loose stools C3163620 Hypotension adverse event HSDN C3665347 Vision impaired C0795873 Aldred syndrome MalaCards C0917801 Sleep disorder insomnia C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C0010038 Corneal opacity disorder C0023786 Mucopolysaccharidosis i OrphaNet C1963091 Diarrhea adverse event C0006309 Brucellosis HSDN C2024878 Cardiovascular surgery result: dyspnea C2609414 Acute kidney injury HSDN C1860844 Sparse, thin hair C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C0036572 Convulsion C0018235 Aggrieved HSDN C2984058 Have pain C0877792 Sleep disorders, circadian rhythm HSDN C0234376 Tremor action C3280692 Mchccd MalaCards|UMLS C0009421 Comatose C0038160 Staphylococcal infections HSDN C2984057 Have nausea C0035222 Respiratory distress syndrome, adult HSDN C1279888 Proteinuria of undiagnosed cause C0037313 Sleep HSDN C0030193 Sense of pain C0018916 Hemangioma HSDN C4085317 Diarrhea frequency C0031542 Phlebitis HSDN C3539023 Pelvic pain increasing in frequency C0205788 Histiocytoid hemangioma HSDN C3539020 Pelvic pain decreasing in frequency C1547940 Specimen source codes - ulcer HSDN C0349588 Stature short C0685837 Pure gonadal dysgenesis, 46, xx HPO C0012833 Dizzy C0152181 Hypoglossal nerve disease or syndrome HSDN C0234979 Dysdiadochokinesia C0853240 Mobius ii syndrome MalaCards C0007859 Pain neck C0221069 Anterior spinal artery syndrome HSDN C0018991 Paralysis one side of body C0021053 Immune system diseases HSDN C0018777 Deafness, conductive C0460136 Barotrauma HSDN C2984058 Have pain C0242666 Protein s deficiency HSDN C0011991 Loose stools C0206682 Follicular thyroid carcinoma HSDN C1963180 Neck pain adverse event C0029410 Osteoarthritis of hip HSDN C1963064 Anxiety adverse event C1859252 Cerebrofaciothoracic dysplasia MalaCards C0010520 Skin cyanosis C1263992 Toxic methemoglobinemia with cyanosis UMLS C4084768 Usual severity vomiting C1145628 Autonomic nervous system disorders HSDN C4085210 Usual severity pain C0005426 Biliary tract neoplasm HSDN C0033377 Caudal displacement C0040100 Thymoma OrphaNet|MalaCards C0018681 Headache, cephalalgia C0035222 Respiratory distress syndrome, adult HSDN C0349588 Stature short C2675511 Diamond-blackfan anemia 8 MalaCards C4085210 Usual severity pain C0020452 Hyperemia HSDN C3898969 Have been vomiting C1563215 Powassan encephalitis virus infection MalaCards C2203646 Jaundice C0032966 Complication, neoplastic pregnancy HSDN C0000737 Abdomen pain C0011854 Diabetes mellitus, insulin-dependent HSDN|UMLS C2237041 Shox gene with short stature C0472813 X-linked agammaglobulinemia with growth hormone deficiency HPO C0031911 Pigment deposition C2713443 Familial intestinal polyposis MalaCards C0026821 Cramp C0016506 Foot deformities HSDN C4084773 Bothered by weight gain C0018674 Head trauma HSDN C0030193 Sense of pain C0033906 Psychological theories HSDN C0013528 Echo speech C0795940 Filippi syndrome MalaCards C0003469 Anxiety disorder C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C0015676 Mental fatigue C4084909 Depression subordinate domain HSDN C0012833 Dizzy C0271490 Diffuse labyrinthitis UMLS C0151740 Intracranial hypertension C0751291 Desmoplastic medulloblastoma MalaCards C0015469 Facial paralysis C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C4085211 Pain distress question C0021125 Impulsive behavior HSDN C0454644 Delayed language development C0553586 Cafe-au-lait macules with pulmonary stenosis MalaCards C3463815 Feel fatigue C0027051 Myocardial infarction HSDN C0011991 Loose stools C2350521 Gustatory perception HSDN C4084766 Vomiting C0004623 Bacterial infections HSDN C0011206 Delirium acute C0019151 Hepatic encephalopathy HSDN C0241210 Speaking delay C2750082 Deafness, autosomal recessive 79 MalaCards|HPO C0917816 Deficiency mental C0019569 Hirschsprung disease MalaCards|HPO C1963164 Lymphopenia adverse event C1851970 Dyskeratosis congenita, autosomal dominant MalaCards|HPO C0039070 Collapse fleeting C0340485 Familial ventricular tachycardia MalaCards C0035232 Diaphragmatic paralysis C0011633 Dermatomyositis HSDN C4084776 Weight loss C0687720 Central diabetes insipidus OrphaNet|MalaCards C4085210 Usual severity pain C0024961 Injuries maxillofacial HSDN C3815497 Cough C0013808 Electroconvulsive therapy HSDN C0007859 Pain neck C0029443 Osteomyelitis HSDN C1999266 Depression adverse event C0339534 Usher syndrome type 2 MalaCards|HPO C1963087 Constipation adverse event C0271737 Addison's disease due to autoimmunity OrphaNet C0156405 Bleeding ovulation C0019080 Hemorrhage UMLS C2242996 Tingling C0750426 Wbc elevated HSDN C0018681 Headache, cephalalgia C0035369 Retroviridae infections HSDN C0241210 Speaking delay C0268632 Homocarnosinosis MalaCards C0850758 Pain pelvic C3244301 Coverage level - family HSDN C0007859 Pain neck C0004623 Bacterial infections HSDN C0018991 Paralysis one side of body C0029396 Heterotopic ossification HSDN C0424755 Fever symptoms C0751396 Well differentiated oligodendroglioma HSDN C1959630 Eye pain adverse event C0015395 Burn eye HSDN C1963249 Tinnitus adverse event C0036341 Schizophrenia HSDN C0027066 Myoclonic jerking C0042830 Perception visual HSDN C1963091 Diarrhea adverse event C1858592 Carney triad OrphaNet|MalaCards C0002622 Amnesias C0020676 Hypothyroidism HSDN C0000737 Abdomen pain C0005695 Bladder neoplasm HSDN C2911645 Weight loss adverse event C0243057 Stomatognathic system abnormalities HSDN C2984058 Have pain C0238198 Gastrointestinal stromal tumors HSDN C0037316 Not enough sleeping C0042510 Ventricular fibrillation HSDN C0018784 Deafness sensorineural C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1834929 Congenital microgastria and limb reduction defects MalaCards C0019079 Bloody sputum C0020951 Immune complex diseases HSDN C4085210 Usual severity pain C0009353 Colles' fracture HSDN C0030193 Sense of pain C0158570 Vascular anomaly HSDN C0560024 Eyelid swelling C2673377 Mucolipidosis ii alpha/beta (disorder) UMLS C3898969 Have been vomiting C2984289 Melanoma pathway HSDN C4085211 Pain distress question C0340464 Heartbeats ectopic HSDN C4085548 Usual severity dizziness C0027658 Neoplasms, germ cell and embryonal HSDN C0857305 Thrombocytopenia purpura C2937421 Prostatic hyperplasia HSDN C0751837 Gait ataxic C2748910 Rett syndrome, atypical MalaCards|HPO C0035232 Diaphragmatic paralysis C0019693 Hiv infections HSDN C0020538 Hbp C0206743 Rhabdoid tumor OrphaNet|MalaCards C4084897 Sleep disturbance subordinate domain C1868594 Perry syndrome OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0162539 Igg deficiency HSDN C0000737 Abdomen pain C0861859 Bile duct signet ring cell carcinoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0001420 Papillary adenocarcinoma HSDN C0344232 Blurred vision C1704429 Hypoalphalipoproteinemia, familial OrphaNet|HPO C4084726 Distress cough C0038941 Incisional infection HSDN C0023012 Delay language C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0270958 Kocher-debre-semelaigne syndrome OrphaNet|MalaCards C0018965 Blood urine C0023241 Legionnaires' disease MalaCards C1963091 Diarrhea adverse event C0038356 Stomach neoplasms HSDN C0221752 Rbc urine C0036421 Systemic scleroderma MalaCards C0232493 Epigastric pain C0279606 Childhood hepatocellular carcinoma MalaCards C4085210 Usual severity pain C0242422 Parkinsonian disorders HSDN C3829611 Nausea frequency C0033975 Psychotic disorders HSDN C2919142 Short stature adverse event C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C0040822 D tremors C0008925 Cleft palate HSDN C0522224 Palsied C1443900 Inhalational botulism OrphaNet|MalaCards C0027066 Myoclonic jerking C1535917 Nipah virus infection MalaCards C3829611 Nausea frequency C0012691 Dislocations HSDN C4084775 Usual severity weight loss C0009375 Colonic neoplasms HSDN C4084766 Vomiting C0032319 Pneumopericardium HSDN C0020578 Hyperventilate C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C1000483 Genus anemia C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C4020887 Photodysphoria C0037231 Sjogren-larsson syndrome OrphaNet|HPO|MalaCards C0009421 Comatose C0029185 Orbit tumor HSDN C4084775 Usual severity weight loss C0022729 Klebsiella infections HSDN C0878773 Bladder hyperactive C0023890 Liver cirrhosis HSDN C4084767 Bothered by vomiting C0032460 Polycystic ovary syndrome HSDN C4085549 Dizziness C0038661 Suicide HSDN C2024878 Cardiovascular surgery result: dyspnea C0085404 Poems syndrome HSDN C4084784 Diarrhea C0013504 Echinococcosis, hepatic HSDN C2984058 Have pain C0008325 Cholecystitis HSDN C4085317 Diarrhea frequency C0014591 Epistaxis HSDN C1263846 Attention deficit disorder with hyperactivity C1527168 Bonnevie-ullrich syndrome MalaCards C0040822 D tremors C0038868 Progressive supranuclear palsy HPO C4084775 Usual severity weight loss C0015934 Fetal growth retardation HSDN C1860844 Sparse, thin hair C0265339 Borjeson-forssman-lehmann syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0003949 Asbestosis HSDN C0036572 Convulsion C3151857 Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism MalaCards C1069915 Vertigo C0025427 Mercury poisoning HSDN C0424755 Fever symptoms C0086543 Cataract nos HSDN C4084766 Vomiting C1856405 Glutaric aciduria iic HPO C1384666 Decreased hearing C4084909 Depression subordinate domain HSDN C0032227 Effusion pleural C0024301 Lymphoma, follicular MalaCards|HPO C0004134 Dyssynergia C3553264 Joubert syndrome 17 MalaCards|UMLS C0000727 Abdomen acute C0014714 Ergotism HSDN C0011206 Delirium acute C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C1549543 Administration method - pain C3489413 Lipomatosis, multiple HSDN C0004604 Pain back C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C3539892 Pelvic pain in front C0005690 Bladder fistula HSDN C2203646 Jaundice C2673914 Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive MalaCards C2024893 Cardiovascular surgery result: fatigue C0017086 Gangrene HSDN C4084768 Usual severity vomiting C0004277 Tooth attrition HSDN C0015672 Decreased energy C1327920 Childhood chronic myelogenous leukemia UMLS C0085631 Abnormal excitement C1845243 Mental retardation, x-linked, syndromic, claes-jensen type MalaCards|HPO C0020639 Hypoproteinaemia C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C3539889 Pelvic pain increasing in severity C0016664 Fatigue fracture HSDN C2984058 Have pain C0018965 Hematuria HSDN C0392699 Dysaesthesia C3489856 Cold hypersensitivity MalaCards C0004604 Pain back C0206698 Cholangiocarcinoma HSDN C0007859 Pain neck C0012644 Animal disease models HSDN C0023014 Developmental disorder language C0004941 Behavioral symptoms HSDN C0085642 Asphyxia reticularis C0004782 Basal ganglia diseases HSDN C0034155 Thrombotic thrombocytopenic purpura C1963234 Serum sickness adverse event HSDN C4084726 Distress cough C0007222 Cardiovascular diseases HSDN C0023012 Delay language C1850985 Fragile site 16p12 HPO C0018772 Deafness C0020295 Hydronephrosis HSDN C0013404 Respiratory difficulty C0023220 Leg injury HSDN C3541349 Syncope C1867904 Long qt syndrome 5 MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0005424 Biliary tract diseases HSDN C0026821 Cramp C0016052 Fibromuscular dysplasia HSDN C1279888 Proteinuria of undiagnosed cause C1856143 Hemolytic uremic syndrome, typical MalaCards C0427190 Ataxia, truncal C1847352 Polymicrogyria, bilateral frontoparietal MalaCards|HPO|UMLS C2984057 Have nausea C0035229 Respiratory insufficiency HSDN C4084769 Vomiting frequency C0032285 Pneumonia HSDN C0007758 Cerebellar ataxia C1859566 Bardet-biedl syndrome 8 HPO C1963066 Joint pain adverse event C1845168 Hypophosphatemic rickets, x-linked recessive MalaCards C0005745 Blepharoptosis C0205969 Thymic carcinoma MalaCards C1963077 Bone pain adverse event C2363065 Vitamin d-resistant rickets MalaCards C0041834 Erythematous condition C2347126 Microscopic polyarteritis MalaCards C4084769 Vomiting frequency C0011860 Diabetes mellitus, non-insulin-dependent HSDN C3641755 Have constipation C0011570 Mental depression HSDN C1549543 Administration method - pain C0175754 Agenesis of corpus callosum HSDN C3641756 Have diarrhea C1963198 Pancreatitis adverse event HSDN C0011991 Loose stools C0019569 Hirschsprung disease MalaCards|HSDN|HPO C0013362 Dysarthrias C1839264 Spastic paraplegia 2, x-linked (disorder) MalaCards|HPO C1963093 Dizziness adverse event C0037952 Spinocerebellar degeneration HSDN C2237041 Shox gene with short stature C1846170 Mental retardation, x-linked, syndromic 7 OrphaNet|MalaCards C0040264 Ear ringing sound C1333989 Familial meningioma MalaCards C0241157 Skin pustule C0085435 Arthritis, reactive OrphaNet|MalaCards C0237326 Defecation pain C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C4084727 Cough frequency C0024788 Green monkey virus disease OrphaNet|MalaCards C0038002 Spleen enlargement C0021368 Inflammation MalaCards C0234146 Absent reflex C4013360 Giant axonal neuropathy 2, autosomal dominant MalaCards C3815497 Cough C0006271 Bronchiolitis MalaCards C0013395 Indigestion C1962958 Hematoma adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0677838 Grief loss HSDN C0002962 Angina C0011881 Diabetic nephropathy HSDN C4085211 Pain distress question C0040422 Tonsillar neoplasms HSDN C4084768 Usual severity vomiting C1879737 Aromatherapy and essential oils HSDN C0019825 Voice hoarseness C0026705 Mucopolysaccharidosis ii UMLS C0039070 Collapse fleeting C0030305 Pancreatitis HSDN C0042963 Symptoms vomiting C0012561 Broad tapeworm infection DiseaseOntology C0240715 Perineal lump C0341850 Vulval warts UMLS C4085661 Usual severity nausea C0007117 Basal cell carcinoma HSDN C3541349 Syncope C0014170 Endometrial neoplasms HSDN C0038002 Spleen enlargement C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards|HPO C0040264 Ear ringing sound C0002986 Fabry disease HSDN C0042571 Vertigo subjective C0032463 Polycythemia vera OrphaNet|HPO C0039070 Collapse fleeting C0024299 Lymphoma HSDN C1963170 Hypothermia adverse event C2940786 Thyroid hormone resistance syndrome HPO C0030193 Sense of pain C0003827 Art therapies HSDN C0039070 Collapse fleeting C0034634 Rage HSDN C0007758 Cerebellar ataxia C0003467 Anxiety HSDN C0030552 Paralysis partial C0751039 Cockayne syndrome, type i HPO C0151740 Intracranial hypertension C0004943 Behcet syndrome MalaCards|HPO C0000727 Abdomen acute C1527336 Sjogren's syndrome HSDN C1557397 Adverse event associated with pain C0022336 Creutzfeldt-jakob disease HSDN C0030486 Extremity paralysis, lower C0004623 Bacterial infections HSDN C0037763 Spasm C0032371 Poliomyelitis MalaCards|HSDN C0024031 Back pain lower back C0000768 Congenital abnormality HSDN C0015938 Fetal macrosomia C0015927 Intrauterine fetal demise HSDN C0022346 Yellow skin C4049994 Insulin resistance measurement HSDN C0026838 Spasticity muscle C0032962 Pregnancy complications HSDN C0151311 Cranial nerve palsy C1847319 Paraganglioma and gastric stromal sarcoma OrphaNet|HPO|MalaCards C0035229 Respiratory function impaired C0221056 Adult type dermatomyositis OrphaNet|MalaCards C0011991 Loose stools C0010034 Corneal diseases HSDN C3898969 Have been vomiting C0025222 Melena HSDN C3887784 Decreased urine output C1090821 Sepsis (invertebrate) HSDN C4085222 Nausea C0017601 Glaucomas HSDN C3829611 Nausea frequency C0038395 Streptococcal infections HSDN C0007758 Cerebellar ataxia C1306856 Megaloblastic anemia due to inborn errors of metabolism MalaCards C4085211 Pain distress question C0018199 Granuloma, plasma cell HSDN C0036572 Convulsion C0747057 Organic heart disease UMLS C0151205 Periorbital edema C0812341 Latex allergy response UMLS C4084802 Usual severity diarrhea C0025521 Inborn errors of metabolism HSDN C0033774 Skin pruritus C0019069 Hemophilia a HSDN C4084802 Usual severity diarrhea C0206611 Pestivirus infections HSDN C4084723 Constipation C0012644 Animal disease models HSDN C1963087 Constipation adverse event C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0028738 Nystagmus C0039483 Giant cell arteritis MalaCards|HPO C0231528 Muscle pain generalized C1304456 Congo hemorrhagic fever MalaCards C0151786 Weakness muscle C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C4085549 Dizziness C0013010 Cerebral lateralization HSDN C1971624 Appetite absent C0345904 Malignant neoplasm of liver MalaCards C0036572 Convulsion C0342345 Hypoparathyroidism - autosomal dominant MalaCards|HPO C0750394 Wbc low C3810350 Bone marrow failure syndrome 2 MalaCards C2012641 Growth on left sclera C0036412 Sclera UMLS C0018926 Emesis bloody C0700639 Pyloric stenosis, hypertrophic HSDN C0011206 Delirium acute C0344435 Ventricular fibrillation by ecg finding HSDN C3463815 Feel fatigue C2219717 Menstrual periods stopped for over 6 months HSDN C0030552 Paralysis partial C1844865 Charcot-marie-tooth disease, x-linked recessive, 3 (disorder) OrphaNet C0002962 Angina C0878544 Cardiomyopathies HSDN C1962956 Flatulence adverse event C0036239 Satiety HSDN C0030552 Paralysis partial C0024305 Lymphoma, non-hodgkin HSDN C0018681 Headache, cephalalgia C0023267 Fibroid tumor HSDN C0036572 Convulsion C0020875 Ileal diseases HSDN C1549543 Administration method - pain C0038833 Superior vena cava syndrome HSDN C0037763 Spasm C0343312 Tetanus neonatorum nos DiseaseOntology|MalaCards C0973461 Dysphasia C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0518090 Frequency of pain question C0008065 Childhood behavior HSDN C4084788 Have dizziness C0021799 Interprofessional relations HSDN C0522224 Palsied C1527336 Sjogren's syndrome HSDN C0027066 Myoclonic jerking C0023772 Lipid metabolism, inborn errors HSDN C3146279 Coma C0026857 Musculoskeletal diseases HSDN C0262384 Chest pain atypical C0029408 Degenerative polyarthritis UMLS C4018871 Abnormality of the respiratory system C1862082 Brachymorphism-onychodysplasia-dysphalangism syndrome MalaCards C2045681 Change in urinary habits C0085606 Urgency of micturition UMLS C0018524 Hallucinate C0018799 Heart diseases HSDN C0004604 Pain back C1304456 Congo hemorrhagic fever MalaCards C1836296 Lower extremity weakness C0038454 Cerebrovascular accident UMLS C0000737 Abdomen pain C0276609 Acute type b viral hepatitis UMLS C0043094 Weight gain C0018133 Graft-vs-host disease HSDN C0022346 Yellow skin C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084775 Usual severity weight loss C0162557 Liver failure, acute HSDN C4084773 Bothered by weight gain C0037744 Perceptual spatial orientation HSDN C2024893 Cardiovascular surgery result: fatigue C0025500 Mesothelioma HSDN C0424755 Fever symptoms C0014170 Endometrial neoplasms HSDN C0002622 Amnesias C0015726 Focused anxiety HSDN C4084723 Constipation C0265499 49,xxxxy chromosomal anomaly OrphaNet|MalaCards C4085317 Diarrhea frequency C0268647 Lysinuric protein intolerance MalaCards|HPO C4084766 Vomiting C0600041 Infective cystitis HSDN C1963091 Diarrhea adverse event C0004576 Babesiosis HSDN C1962972 Proteinuria adverse event C0162316 Iron deficiency anemia HSDN C0233565 Bradykinesia C2751842 Parkinson disease 14, autosomal recessive MalaCards|HPO|UMLS C1705500 Flasher - visual manifestation C0220633 Uveal melanoma HPO C4084769 Vomiting frequency C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0003862 Pain joint C2936881 Eosinophilic synovitis MalaCards C4084725 Usual severity cough C0040553 Toxocariasis HSDN C0518090 Frequency of pain question C0342443 Adrenal cushing's syndrome HSDN C0030193 Sense of pain C0014571 Epiphyses, slipped HSDN C4084774 Have weight loss C0015579 Family characteristics HSDN C0023530 Leukopenia C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C4084724 Usual severity constipation C0019326 Ventral hernia HSDN C0018775 Hearing loss bilateral C1418479 Pex7 gene HSDN C0013456 Pain ear C0031345 Pharyngeal diseases HSDN C1963091 Diarrhea adverse event C0040558 Toxoplasmosis HSDN C4084775 Usual severity weight loss C0013080 Down syndrome HSDN C2984057 Have nausea C0033873 Psychiatry HSDN C0240735 Personality change C1843014 Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques HPO C0013362 Dysarthrias C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO C4084773 Bothered by weight gain C0035042 Psychology and religion HSDN C0036572 Convulsion C0033970 Time limited psychotherapy HSDN C1963086 Confusion adverse event C0021229 Individuation HSDN C0010200 Cough symptom C0085092 Parenting behavior HSDN C0034150 Skin purpura C0007873 Uterine cervical neoplasm HSDN C0036572 Convulsion C0020490 Hyperopia HSDN C0027796 Neuralgias C0030305 Pancreatitis HSDN C0013362 Dysarthrias C2931082 Familial apoceruloplasmin deficiency MalaCards C2984058 Have pain C0038016 Spondylolisthesis HSDN C0043094 Weight gain C0043097 Perception, weight HSDN C1557397 Adverse event associated with pain C0013502 Echinococcosis HSDN C1069915 Vertigo C0162872 Aortic aneurysm, thoracic HSDN C4084802 Usual severity diarrhea C0038579 Substance abuse, intravenous HSDN C0917816 Deficiency mental C0796121 Primrose syndrome OrphaNet|HPO|MalaCards C1000483 Genus anemia C0272005 Hemoglobin bart's hydrops syndrome MalaCards C1963091 Diarrhea adverse event C0009917 Contracture HSDN C4084802 Usual severity diarrhea C0024620 Primary malignant neoplasm of liver MalaCards C0004134 Dyssynergia C0035309 Retinal diseases HSDN C0036572 Convulsion C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0000737 Abdomen pain C0014869 Peptic esophagitis HSDN C1860844 Sparse, thin hair C3280799 Cutis laxa, autosomal recessive, type iiib MalaCards C0013362 Dysarthrias C0037061 Siderosis HSDN C4084774 Have weight loss C0026946 Mycoses HSDN C0022346 Yellow skin C0023343 Leprosy HSDN C3539896 Pelvic pain occurs with urination C0024121 Lung neoplasms HSDN C0018991 Paralysis one side of body C0042830 Perception visual HSDN C2919142 Short stature adverse event C0685837 Pure gonadal dysgenesis, 46, xx HPO C4084724 Usual severity constipation C0024141 Lupus erythematosus, systemic HSDN C0042571 Vertigo subjective C0027902 Neuropsychological diagnosis HSDN C4084766 Vomiting C0026266 Mitral valve insufficiency HSDN C3829611 Nausea frequency C1546847 Entity name part type - family HSDN C0030193 Sense of pain C1306577 Dies patient HSDN C0020578 Hyperventilate C0017168 Gastroesophageal reflux disease HSDN C0042928 Paralysis vocal cord C0008479 Chondrosarcoma HSDN C1549543 Administration method - pain C0041601 Ulna fracture HSDN C1838869 Proximal neurogenic muscle weakness C1854058 Spinal muscular atrophy, late-onset, finkel type MalaCards|HPO C0004134 Dyssynergia C1849437 Mainzer-saldino disease MalaCards|HPO C1963281 Vomiting adverse event C0021400 Influenza HSDN C0206160 Retic count elevated C3151421 Cyanosis, transient neonatal MalaCards|HPO C0011991 Loose stools C0040948 Trichostrongyliasis HSDN C3539889 Pelvic pain increasing in severity C0009324 Ulcerative colitis HSDN C3898969 Have been vomiting C1522133 High cholesterol level HSDN C0025287 Meningitis-like C0967777 Mok protein, human HSDN C1557397 Adverse event associated with pain C0019034 Hemoglobin sc disease MalaCards|HSDN C0030193 Sense of pain C0015423 Eyelid diseases HSDN C0428977 Pulse rate decrease C0151516 Thyroid hypoplasia HPO C4084774 Have weight loss C0153458 Pancreas head cancer malignant MalaCards C3641756 Have diarrhea C0002871 Anemia HSDN C0015672 Decreased energy C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C0152116 Torticollis spasmodic C1527306 Spasmus nutans OrphaNet|MalaCards C2128592 Both feet turn out while walking C0020497 Cortical congenital hyperostosis MalaCards C3539023 Pelvic pain increasing in frequency C0242350 Erectile dysfunction HSDN C0018965 Blood urine C2212594 Small cell carcinoma of bladder MalaCards C0521764 Nystagmus enhanced when fixation removed C0015397 Disorder of eye UMLS C4085661 Usual severity nausea C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0009806 Constipate C0035435 Rheumatism HSDN C0002962 Angina C0021818 Intervertebral disk displacement HSDN C0040822 D tremors C0268140 Xeroderma pigmentosum, group f HPO C0018784 Deafness sensorineural C0039336 Gustatory sense HSDN C0497406 Over weight C0015663 Fasting HSDN C0013404 Respiratory difficulty C0702166 Acne HSDN C3463815 Feel fatigue C0013806 Electroplexy shock therapy HSDN C0039070 Collapse fleeting C0268243 Niemann-pick disease, type b HSDN C4084774 Have weight loss C0017661 Iga glomerulonephritis HSDN C3829611 Nausea frequency C0022104 Irritable bowel syndrome HSDN C4084776 Weight loss C0022680 Polycystic kidney diseases HSDN C3146279 Coma C0033975 Psychotic disorders HSDN C1557397 Adverse event associated with pain C0018552 Hamartoma HSDN C4084776 Weight loss C0008497 Choriocarcinoma HSDN C2317014 Spasm of cervix uteri C2026908 Cervical spasm with baby delivered UMLS C1963281 Vomiting adverse event C0019348 Herpes simplex infections HSDN C0020458 Hyperhydrosis C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C3641755 Have constipation C0403555 Ochoa syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0398623 Thrombophilia HSDN C0018772 Deafness C0079583 Ichthyosiform erythroderma, congenital MalaCards|HSDN C0085631 Abnormal excitement C0796249 Mental retardation, x linked 47 HPO C0040822 D tremors C2678415 Hyperphenylalaninemia, bh4-deficient, due to partial pts deficiency HPO C4085549 Dizziness C0042029 Urinary tract infection HSDN C0242936 Center pain C0030528 Paratyphoid fever HSDN C3815497 Cough C0032962 Pregnancy complications HSDN C4084768 Usual severity vomiting C0024228 Lymphatic diseases HSDN C0042571 Vertigo subjective C0342257 Complications of diabetes mellitus HSDN C0424755 Fever symptoms C0034194 Pyloric stenosis HSDN C0030486 Extremity paralysis, lower C0019163 Hepatitis b HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0344435 Ventricular fibrillation by ecg finding HSDN C0009792 Consciousness disorder C0006118 Brain neoplasms HSDN C0036572 Convulsion C2751584 Neurodegeneration due to cerebral folate transport deficiency MalaCards|HPO|UMLS C0003862 Pain joint C0004760 Air pressure-related disorder HSDN C0085593 Chill C0041834 Erythema HSDN C1384666 Decreased hearing C0027092 Myopia HSDN C4084802 Usual severity diarrhea C0011848 Diabetes insipidus HSDN C0151786 Weakness muscle C0751254 Creutzfeldt-jakob disease, familial MalaCards C1263846 Attention deficit disorder with hyperactivity C2931338 Chromosome 3, monosomy 3q13 MalaCards C1963093 Dizziness adverse event C0009373 Colonic diseases HSDN C0026838 Spasticity muscle C0796254 Dandy-walker malformation with mental retardation, basal ganglia disease, and seizures UMLS C4084726 Distress cough C0149931 Migraine disorders HSDN C2984058 Have pain C0018944 Hematoma HSDN C4084723 Constipation C0042812 Acuity visual HSDN C0013604 Edematous C1963282 Wolff-parkinson-white syndrome adverse event HSDN C1962972 Proteinuria adverse event C0019196 Hepatitis c HSDN C0010200 Cough symptom C0162316 Iron deficiency anemia HSDN C0020305 Fetal edema C0020639 Hypoproteinemia HSDN C1000483 Genus anemia C0268237 Cytochrome-c oxidase deficiency MalaCards|HPO C1962972 Proteinuria adverse event C3553774 Interstitial nephritis, karyomegalic MalaCards C0040822 D tremors C0007786 Brain ischemia HSDN C2024893 Cardiovascular surgery result: fatigue C0520946 Emotional hypersensitivity HSDN C2315100 Pediatric failure to thrive C0265201 De sanctis-cacchione syndrome MalaCards C0518090 Frequency of pain question C0038002 Splenomegaly HSDN C0040485 Wryneck C0006157 Breech presentation HSDN C2919142 Short stature adverse event C3149814 Retinal dystrophy, early-onset, with pituitary dysfunction HPO C2237041 Shox gene with short stature C0268547 Argininosuccinic aciduria OrphaNet|HPO|MalaCards C0011206 Delirium acute C0037274 Dermatologic disorders HSDN C0917816 Deficiency mental C0008628 Chromosome deletion MalaCards C0333240 Acute edema C0340102 Toxic pulmonary edema UMLS C0030200 Intractable pain C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084788 Have dizziness C2930902 Bidirectional tachycardia MalaCards C0042571 Vertigo subjective C0027809 Neurilemmoma OrphaNet|MalaCards C1260880 Nasal drip C1709153 Nasopharyngeal differentiated carcinoma UMLS C1963184 Nystagmus adverse event C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C0034150 Skin purpura C0242666 Protein s deficiency HSDN C0234376 Tremor action C1707400 Classic medulloblastoma MalaCards C1963252 Tremor adverse event C4041080 Neurocognitive disorders HSDN C0026838 Spasticity muscle C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO|UMLS C0018772 Deafness C0037116 Silicosis HSDN C2029884 Hearing loss by exam C0002989 Epithelioid hemangioma of skin HSDN C0036572 Convulsion C0699828 Serotonergic syndrome HSDN C0013390 Cramps menstrual C0227791 Discharge vaginal HSDN C0033377 Caudal displacement C0339085 Blepharochalasis, struma, double lip syndrome OrphaNet|MalaCards C0038506 Stutter C2939156 Development of sexuality HSDN C0241137 Skin pallor C0031873 Pica disease HSDN C2984058 Have pain C0029422 Osteochondrodysplasias HSDN C2024878 Cardiovascular surgery result: dyspnea C0004045 Asphyxia neonatorum HSDN C0003862 Pain joint C0036310 Scheuermann's disease HSDN C1549543 Administration method - pain C0032708 Disorders of porphyrin metabolism HSDN C0242936 Center pain C2004491 Cicatrix HSDN C0025287 Meningitis-like C3495559 Juvenile arthritis HSDN C1384666 Decreased hearing C2931390 Anophthalmia, cleft lip-palate, facial anomalies, and cns anomalies and hypothalamic disorder MalaCards C0019825 Voice hoarseness C1839130 Dystonia 3, torsion, x-linked HSDN C0018834 Brash C0012746 Dissociative disorder HSDN C0011206 Delirium acute C0037646 Psychiatric somatic therapy HSDN C0012833 Dizzy C1706377 Memory device component HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C3665347 Vision impaired C1970840 Leukoencephalopathy with metaphyseal chondrodysplasia MalaCards C4085211 Pain distress question C0399352 Developmental absence of tooth HSDN C2032395 Pelvic pain on the left C0042996 Vulvitis unspecified HSDN C4085211 Pain distress question C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C1963137 Hydrocephalus adverse event C0238402 Pycnodysostosis MalaCards|HPO C1000483 Genus anemia C2919861 Medullary cystic kidney disease type 1 MalaCards C0004941 Behavioral symptoms C0268642 Histidinuria renal tubular defect MalaCards C0026838 Spasticity muscle C0406612 Encephalocraniocutaneous lipomatosis OrphaNet|MalaCards C0041834 Erythematous condition C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards C1145670 Failure respiratory C0024419 Waldenstrom macroglobulinemia OrphaNet|HPO|MalaCards C0011991 Loose stools C2937225 Biotin deficiency disease MalaCards C0000737 Abdomen pain C2936913 Porphyria, south african type HPO C4085210 Usual severity pain C0158328 Trigger finger HSDN C2911647 Weight gain adverse event C0030767 Grouping peer HSDN C1962972 Proteinuria adverse event C0033680 Protein-losing enteropathies HSDN C0005745 Blepharoptosis C0162809 Kallmann syndrome MalaCards|HPO C0005745 Blepharoptosis C1837094 Myasthenic syndrome, congenital, ie MalaCards|HPO C0030552 Paralysis partial C0018674 Head trauma HSDN C4084723 Constipation C1552262 Nurse practitioner - family HSDN C3274924 Have been coughing C0005592 Bird fancier's lung DiseaseOntology|MalaCards C0033774 Skin pruritus C0600467 Neurogenic inflammation HSDN C4084724 Usual severity constipation C0002878 Anemia, hemolytic HSDN C0013395 Indigestion C0001418 Adenocarcinoma HSDN C0241165 Skin thickening C2931241 Primary intestinal lymphangiectasis MalaCards C0015970 Fever unknown origin C0030528 Paratyphoid fever HSDN C1549543 Administration method - pain C0040261 Onychomycosis HSDN C0042798 Vision dim C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0702221 Tactual discrimination HSDN C0036396 Sciatica C0002871 Anemia HSDN C0015672 Decreased energy C0015927 Intrauterine fetal demise HSDN C0041657 Consciousness loss C1963138 Hypertension adverse event HSDN C4084788 Have dizziness C0035242 Respiratory tract diseases HSDN C0040460 Dental pain C0014544 Epilepsy HSDN C0037199 Sinus infection C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards C4085661 Usual severity nausea C0206245 Amyloid neuropathies, familial HSDN C0242936 Center pain C0019326 Ventral hernia HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C2930902 Bidirectional tachycardia MalaCards C0009806 Constipate C0013364 Dysautonomia, familial HPO|UMLS C1860844 Sparse, thin hair C1866182 Penttinen-aula syndrome MalaCards|HPO C4084725 Usual severity cough C0021368 Inflammation HSDN C0024031 Back pain lower back C0022744 Knee injury HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042162 Uveal neoplasms HSDN C0010520 Skin cyanosis C1553188 Hemolysis - observation HSDN C4085548 Usual severity dizziness C0024141 Lupus erythematosus, systemic HSDN C0012833 Dizzy C0018800 Cardiomegaly HSDN C0034150 Skin purpura C0035021 Relapsing fever HSDN C0004134 Dyssynergia C3553960 Peroxisome biogenesis disorder 8b MalaCards C3887873 Hearing loss C0037928 Spinal cord diseases HSDN C0027497 Queasy C0034088 Pulmonary valve insufficiency HSDN C0042571 Vertigo subjective C0018799 Heart diseases HSDN C0031911 Pigment deposition C1321683 Melanoacanthoma MalaCards C0349683 Body positional nystagmus C0015397 Disorder of eye UMLS C1384666 Decreased hearing C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards C1549543 Administration method - pain C0376670 Pancreatitis, alcoholic HSDN C0036572 Convulsion C1856059 Mthfr deficiency, thermolabile type HPO C2984058 Have pain C1366464 F9 gene HSDN C0023012 Delay language C3888317 Sialidosis, type 2 OrphaNet C1963281 Vomiting adverse event C0019569 Hirschsprung disease MalaCards|HSDN C1384666 Decreased hearing C0265239 Wildervanck's syndrome MalaCards C2984057 Have nausea C0008924 Cleft lip HSDN C0086437 Joint hypermobility C1850168 Bruck syndrome 1 MalaCards|HPO C1557397 Adverse event associated with pain C0155862 Streptococcal pneumonia HSDN C1549543 Administration method - pain C0021099 Impetigo HSDN C4084788 Have dizziness C0041327 Tuberculosis, pulmonary HSDN C4084726 Distress cough C0040100 Thymoma OrphaNet|MalaCards C0007758 Cerebellar ataxia C1852267 Optic atrophy 1 and deafness HPO C0018681 Headache, cephalalgia C0334588 Giant cell glioblastoma UMLS C0034151 Hyperglobulinemic purpura C0241910 Hepatitis, autoimmune HSDN C0027497 Queasy C1705810 Generic role HSDN C1527344 Dysphonia C1334374 Laryngeal neuroendocrine neoplasm MalaCards C2911645 Weight loss adverse event C0027697 Nephritis HSDN C0518090 Frequency of pain question C0042018 Urinary calculi HSDN C1963091 Diarrhea adverse event C0086649 Mps iii c HPO C0026838 Spasticity muscle C4084841 Joubert syndrome 24 UMLS C0036572 Convulsion C0037275 Skin diseases, vesiculobullous HSDN C0007758 Cerebellar ataxia C1145628 Autonomic nervous system disorders HSDN C4084766 Vomiting C1866495 Bartter syndrome, antenatal type 1 HPO C4084784 Diarrhea C0040588 Tracheoesophageal fistula HSDN C0005745 Blepharoptosis C4014660 Combined oxidative phosphorylation deficiency 20 MalaCards C2024893 Cardiovascular surgery result: fatigue C0013274 Patent ductus arteriosus HSDN C0020455 Hypergammaglobulinemia C0151744 Myocardial ischemia HSDN C0040822 D tremors C0031511 Pheochromocytoma MalaCards|HSDN|UMLS C3887873 Hearing loss C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C0036572 Convulsion C0268631 Succinic semialdehyde dehydrogenase deficiency MalaCards|UMLS C4085549 Dizziness C2930902 Bidirectional tachycardia MalaCards C1384666 Decreased hearing C1327918 Oculootoradial syndrome MalaCards|HPO C0011991 Loose stools C0038160 Staphylococcal infections HSDN C0027066 Myoclonic jerking C0033348 Language program HSDN C0037383 Sneeze C0011570 Mental depression HSDN C0018991 Paralysis one side of body C0018801 Heart failure HSDN C0040264 Ear ringing sound C1568249 Usher syndrome, type ii MalaCards C2024893 Cardiovascular surgery result: fatigue C0032787 Postoperative complications HSDN C4085210 Usual severity pain C0021390 Inflammatory bowel diseases HSDN C0020458 Hyperhydrosis C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0002991 Cutaneous fibrous histiocytoma HSDN C0037317 Sleep disturbance C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0038868 Supranuclear palsy progressive C0042594 Vestibular diseases HSDN C4085211 Pain distress question C0003857 Congenital arteriovenous malformation HSDN C3463815 Feel fatigue C0206255 Malaria vaccine HSDN C0018784 Deafness sensorineural C3553951 Peroxisome biogenesis disorder 7b MalaCards C0518090 Frequency of pain question C0009240 Cognition HSDN C0011168 Disorder deglutition C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0020538 Hbp C3150419 Nephronophthisis-like nephropathy 1 MalaCards|HPO C0004093 Asthenia C0037369 Smoking HSDN C4085211 Pain distress question C0867389 Chronic graft-versus-host disease MalaCards C3539023 Pelvic pain increasing in frequency C0027095 Myosarcoma HSDN C0221166 Paraparesis C0018552 Hamartoma HSDN C4085317 Diarrhea frequency C0268384 Familial amyloid neuropathy, portuguese type MalaCards C4084802 Usual severity diarrhea C0039483 Giant cell arteritis HSDN C0151686 Growth retardation C0040954 Infection by trichuris trichiura DiseaseOntology|MalaCards C0018772 Deafness C0018824 Heart valve disease HSDN C0042798 Vision dim C2931916 Midline granulomatosis MalaCards C0018772 Deafness C0026918 Mycobacterium infections HSDN C0231528 Muscle pain generalized C0024796 Marfan syndrome MalaCards C4085222 Nausea C0205770 Choroid plexus papilloma HPO C0012569 Double vision C0270952 Muscular dystrophy, oculopharyngeal HSDN C4084767 Bothered by vomiting C0017155 Gastritis, hypertrophic HSDN C0424755 Fever symptoms C0008073 Developmental disabilities HSDN C2203646 Jaundice C0014661 Equine infectious anemia MalaCards C0009460 Communication impairment C0033975 Psychotic disorders HSDN C1963093 Dizziness adverse event C0027627 Neoplasm metastasis HSDN C0151786 Weakness muscle C0018798 Congenital heart defects HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032269 Pneumococcal infections HSDN C4084802 Usual severity diarrhea C1443901 Intestinal botulism OrphaNet|MalaCards C0020455 Hypergammaglobulinemia C0520946 Emotional hypersensitivity HSDN C4084724 Usual severity constipation C0032927 Precancerous conditions HSDN C0025323 Bleeding menstrual heavy C3888026 Hermansky-pudlak syndrome 8 MalaCards C1963137 Hydrocephalus adverse event C3275487 Cerebral-cerebellar-coloboma syndrome, x-linked MalaCards C0036572 Convulsion C3540662 Congenital amaurosis of retinal origin MalaCards C1961131 Cough adverse event C0032453 Polychondritis, relapsing OrphaNet|MalaCards C4085317 Diarrhea frequency C1690964 Cataract HSDN C1963091 Diarrhea adverse event C0342873 Glutaric aciduria iii MalaCards|HPO C3539889 Pelvic pain increasing in severity C0520720 Cyst nerve root HSDN C0013528 Echo speech C0038186 Reflex, startle HSDN C2911645 Weight loss adverse event C0717360 Disease lyme vaccine HSDN C3641756 Have diarrhea C0042338 Herpesvirus 3, human HSDN C0034933 Abnormal reflexes C0004161 Athletic injuries HSDN C1557397 Adverse event associated with pain C0041107 Trisomy HSDN C3665347 Vision impaired C0795959 Gomez lopez hernandez syndrome OrphaNet|MalaCards C0151786 Weakness muscle C0020443 Hypercholesterolemia HSDN C0011168 Disorder deglutition C1860315 Whispering dysphonia, hereditary MalaCards C0041105 Jaw spasm C2117118 X-ray of toe: deformity contracture HSDN C0038506 Stutter C3244301 Coverage level - family HSDN C1963249 Tinnitus adverse event C0018802 Congestive heart failure HSDN C0023012 Delay language C2931551 Grubben de cock borghgraef syndrome OrphaNet|MalaCards C2029884 Hearing loss by exam C0001175 Acquired immunodeficiency syndrome HSDN C0518090 Frequency of pain question C0031154 Peritonitis HSDN C0027424 Congestion nasal C2136984 Ent surgical result - nose nasal congestion UMLS C2911645 Weight loss adverse event C0022408 Arthropathy HSDN C4084774 Have weight loss C1963266 Uveitis adverse event HSDN C0577568 Mass of urinary system structure C0431735 Congenital polyp of ureter UMLS C0022107 Fussiness C0342871 Acyl-coa oxidase deficiency MalaCards C2911645 Weight loss adverse event C0035412 Rhabdomyosarcoma HSDN C0011570 Monopolar depression C2678480 Chromosome 22q11.2 deletion syndrome, distal MalaCards|HPO C0413252 Hypothermia due to exposure C0009450 Disease caused by microorganism HSDN C3539890 Pelvic pain causes awakening at night C0010695 Cystocele HSDN C0184567 Pain acute C0003873 Rheumatoid arthritis HSDN C0232461 Increased appetite C0017075 Ganglioneuroma MalaCards C2237041 Shox gene with short stature C3540845 Microphthalmia, isolated, with coloboma 8 MalaCards C0018772 Deafness C0007222 Cardiovascular diseases HSDN C1963091 Diarrhea adverse event C0026857 Musculoskeletal diseases HSDN C0033377 Caudal displacement C4014538 Helsmoortel-van der aa syndrome MalaCards C1963252 Tremor adverse event C0151744 Myocardial ischemia HSDN C3274924 Have been coughing C0014858 Esophageal motility disorders HSDN C1557397 Adverse event associated with pain C2936664 Acquired hypogammaglobulinemia HSDN C0030193 Sense of pain C0003708 Arachnitis HSDN C0042025 Urinary incontinence stress C0021799 Interprofessional relations HSDN C4085211 Pain distress question C0009240 Cognition HSDN C0424755 Fever symptoms C0010340 Critical illness HSDN C3541349 Syncope C0037939 Spinal neoplasms HSDN C0013362 Dysarthrias C0001125 Acidosis, lactic HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3244301 Coverage level - family HSDN C1268594 Mechanical presbycusis C0033074 Presbycusis UMLS C0030193 Sense of pain C0206695 Carcinoma, neuroendocrine HSDN C4084766 Vomiting C0001118 Acid base imbalance HSDN C4085211 Pain distress question C0033953 Psychosexual disorders HSDN C0026205 Pupillary constriction C0149931 Migraine disorders HSDN C0024031 Back pain lower back C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0003862 Pain joint C4015276 Familial cold autoinflammatory syndrome 4 MalaCards C0003962 Ascites C2062326 Eosinophilic enteropathy MalaCards C1963087 Constipation adverse event C0027651 Tumor HSDN C0518090 Frequency of pain question C0014358 Enterocolitis, pseudomembranous HSDN C0003469 Anxiety disorder C1837475 Insulin-like growth factor i deficiency MalaCards C4085211 Pain distress question C0043395 Yellow fever HSDN C0009421 Comatose C0032002 Pituitary diseases HSDN C0018784 Deafness sensorineural C0031347 Pharyngeal neoplasms HSDN C0020458 Hyperhydrosis C0410179 Scleroatonic muscular dystrophy MalaCards|HPO C1963184 Nystagmus adverse event C3809008 Hypomyelination with brainstem and spinal cord involvement and leg spasticity MalaCards C0086437 Joint hypermobility C3553571 Congenital disorder of glycosylation, type iik MalaCards|UMLS C0557874 Global developmental delay C1970431 Pitt-hopkins syndrome MalaCards C0851578 Disorder sleep C2706915 Language:-:point in time:^patient:- HSDN C2203646 Jaundice C0037313 Sleep HSDN C0036572 Convulsion C0005396 Bile duct neoplasms HSDN C0007859 Pain neck C2936860 Spastic paraplegia 25, autosomal recessive MalaCards|UMLS C0036396 Sciatica C0700208 Acquired scoliosis HSDN C1549543 Administration method - pain C0035793 Rocky mountain spotted fever HSDN C0036572 Convulsion C1621958 Glioblastoma multiforme MalaCards C3641756 Have diarrhea C1366535 Avp gene HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242188 Spider bites HSDN C0231712 Gait waddling C2931534 Cloverleaf skull and bone dysplasias MalaCards C0000737 Abdomen pain C1504665 Products used to treat diabetic ketoacidosis HSDN C1549543 Administration method - pain C0008149 Chlamydia infections HSDN C0015469 Facial paralysis C3714514 Infection HSDN C1963137 Hydrocephalus adverse event C0040560 Toxoplasmosis, congenital MalaCards C1961131 Cough adverse event C0267830 Pyogenic liver abscess HSDN C4084766 Vomiting C0040247 Tinea HSDN C0027497 Queasy C0027658 Neoplasms, germ cell and embryonal HSDN C0860603 Anxiety symptom C0221406 Pituitary-dependent cushing's disease OrphaNet|HPO C0587047 Mass of trunk C0149797 Umbilical granuloma UMLS C1384666 Decreased hearing C0008074 Child development disorders, pervasive HSDN C1557397 Adverse event associated with pain C0030636 Pasteurella infection HSDN C0030193 Sense of pain C0006325 Bruxism HSDN C0013604 Edematous C0265274 Achondrogenesis, type ib (disorder) HPO C4084766 Vomiting C0007125 Carcinoma, ehrlich tumor HSDN C4020887 Photodysphoria C2751308 Cone dystrophy 4 (disorder) MalaCards|HPO C0242936 Center pain C0040954 Infection by trichuris trichiura HSDN C4084773 Bothered by weight gain C0017563 Gingival diseases HSDN C0028738 Nystagmus C1859568 Bardet-biedl syndrome 10 HPO C1963281 Vomiting adverse event C0268410 Acid phosphatase deficiency HPO C0518090 Frequency of pain question C0030793 Pelvis tumor HSDN C0033774 Skin pruritus C0033772 Prurigo papule, nos UMLS C0085631 Abnormal excitement C0586323 Alcohol withdrawal seizures HSDN C0015469 Facial paralysis C0013502 Echinococcosis HSDN C4084766 Vomiting C0344479 Spinal cord myelodysplasia HSDN C0344232 Blurred vision C0238015 Autonomic dysreflexia UMLS C3887638 Failure to thrive in infant C1849236 Severe combined immunodeficiency, atypical HPO C0030193 Sense of pain C0011649 Dermoid cyst HSDN C0020305 Fetal edema C1096902 Infantile sialic acid storage disease HPO C0848203 Male pelvic pain C0037856 Spermatic cord torsion HSDN C0034933 Abnormal reflexes C0034888 Rectal prolapse HSDN C0023530 Leukopenia C2675859 Diamond-blackfan anemia 5 MalaCards|HPO C0002963 Angina variant C1739395 Takotsubo cardiomyopathy HSDN C1963091 Diarrhea adverse event C0024530 Malaria HSDN C2237041 Shox gene with short stature C2713347 7-dehydrocholesterol reductase deficiency OrphaNet|MalaCards C0026884 Muteness C2939156 Development of sexuality HSDN C0751837 Gait ataxic C0751254 Creutzfeldt-jakob disease, familial MalaCards|HPO C2919142 Short stature adverse event C1846331 Juvenile-onset dystonia MalaCards C4085210 Usual severity pain C0001144 Acne vulgaris HSDN C0030486 Extremity paralysis, lower C0003803 Arnold chiari malformation HSDN C0162298 Stiffness joints C0265286 Dyggve-melchior-clausen syndrome OrphaNet|HPO|MalaCards C0522224 Palsied C0860603 Anxiety symptoms HSDN C0036572 Convulsion C0003504 Aortic valve insufficiency HSDN C4085862 Bothered by nausea C0019294 Hernia, inguinal HSDN C0848203 Male pelvic pain C0017412 Genital diseases, male HSDN C4042891 Sleep wake disorders C0151744 Myocardial ischemia HSDN C0037763 Spasm C0264414 Intrinsic asthma - no status UMLS C4085211 Pain distress question C0243001 Abdominal abscess HSDN C0150055 Pain chronic C0220847 C hepatitis virus HSDN C1963090 Dehydration adverse event C2749685 Cystinosis, atypical nephropathic (disorder) HPO C0233794 Memory impaired C2985219 Papillary tumor of the pineal region OrphaNet|MalaCards C4085211 Pain distress question C0848377 Trauma to the abdomen HSDN C0018772 Deafness C0011860 Diabetes mellitus, non-insulin-dependent HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0008309 Bile duct adenoma HSDN C0009806 Constipate C0206718 Ganglioneuroblastoma HSDN C0037316 Not enough sleeping C0032787 Postoperative complications HSDN C0234132 Pyramidal sign C2677567 Dystonia 16 (disorder) MalaCards|HPO|UMLS C0018784 Deafness sensorineural C0006035 Borrelia infections HSDN C0027497 Queasy C0029882 Otitis media HSDN C1963170 Hypothermia adverse event C1762616 Meningioma, benign, no icd-o subtype HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010072 Coronary thrombosis HSDN C0020578 Hyperventilate C0023895 Liver diseases HSDN C0018681 Headache, cephalalgia C0023473 Myeloid leukemia, chronic HSDN C0042571 Vertigo subjective C0039239 Sinus tachycardia HSDN C0349588 Stature short C1414529 Fancc gene HPO C3898969 Have been vomiting C0023890 Liver cirrhosis HSDN C0398650 Idiopathic thrombocytopenia purpura C0009324 Ulcerative colitis HSDN C1963091 Diarrhea adverse event C4015214 Autoimmune lymphoproliferative syndrome, type v MalaCards C3274920 Have shortness of breath question C0796274 Brown-vialetto-van laere syndrome MalaCards C0034151 Hyperglobulinemic purpura C0079744 Diffuse large b-cell lymphoma HSDN C4084727 Cough frequency C1457883 Aggressive reaction HSDN C0349489 Fetal hypoxia C0497552 Congenital neurologic anomalies HSDN C1384666 Decreased hearing C0268342 Ehlers-danlos syndrome type 6 MalaCards C0030193 Sense of pain C1332241 Ameloblastic carcinoma ex ameloblastoma UMLS C0030200 Intractable pain C0001175 Acquired immunodeficiency syndrome HSDN C1963071 Back pain adverse event C1956346 Coronary artery disease HSDN C0018784 Deafness sensorineural C1275079 Acps iii MalaCards C0036572 Convulsion C0027439 Nasopharyngeal neoplasms HSDN C0015732 Feces incontinence C1867774 Sacral agenesis syndrome OrphaNet|HPO C4084802 Usual severity diarrhea C0019284 Diaphragmatic hernia HSDN C0038506 Stutter C0031212 Personality disorders HSDN C0000737 Abdomen pain C1336858 Undifferentiated gastric carcinoma UMLS C1963281 Vomiting adverse event C0014836 Escherichia coli infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0497572 Female genital herpes HSDN C0349588 Stature short C0079588 Ichthyosis, x-linked MalaCards C1962972 Proteinuria adverse event C0007095 Carcinoid tumor HSDN C4084723 Constipation C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C0518090 Frequency of pain question C0001584 Adolescent psychology HSDN C0020450 Hyperemesis gravidarum C0011849 Diabetes mellitus HSDN C0022346 Yellow skin C1299262 Sarcoma - category (morphologic abnormality) HSDN C4085210 Usual severity pain C1962962 Hyperpigmentation adverse event HSDN C0018772 Deafness C0021359 Infertility HSDN C4085211 Pain distress question C0035795 Fever mountain rocky spotted HSDN C0038002 Spleen enlargement C2673635 Combined saposin deficiency MalaCards|HPO C0877181 Injection site joint redness C3888825 Injection site joint erythema UMLS C1549543 Administration method - pain C0015395 Burn eye HSDN C2911647 Weight gain adverse event C0007820 Cerebrovascular disorders HSDN C2024878 Cardiovascular surgery result: dyspnea C0027686 Pathologic neovascularization HSDN C0030193 Sense of pain C0162872 Aortic aneurysm, thoracic HSDN C0015970 Fever unknown origin C0018203 Chronic granulomatous disease HSDN C0019825 Voice hoarseness C3697269 15q24 microdeletion HPO C0030554 Abnormal sensation C0032708 Disorders of porphyrin metabolism MalaCards C0007758 Cerebellar ataxia C2931917 Alcoholic encephalopathy MalaCards C2029884 Hearing loss by exam C0032964 Pregnancy complications, hematologic HSDN C2919142 Short stature adverse event C1845144 Mental retardation, x linked 92 MalaCards C4084802 Usual severity diarrhea C1522137 Hypertriglyceridemia result HSDN C0015469 Facial paralysis C0410226 Congenital myotonic dystrophy MalaCards C0424755 Fever symptoms C0002064 Alkalosis, respiratory HSDN C0019079 Bloody sputum C1332337 Asbestos-related lung carcinoma UMLS C2024893 Cardiovascular surgery result: fatigue C0006264 Bronchial neoplasms HSDN C0022346 Yellow skin C0035435 Rheumatism HSDN C0013362 Dysarthrias C0003873 Rheumatoid arthritis HSDN C0019214 Hepatosplenomegaly C1846421 Lathosterolosis MalaCards|HPO C0007166 Cardiac output decreased C0037286 Skin neoplasms HSDN C3898969 Have been vomiting C0001125 Acidosis, lactic HSDN C0039070 Collapse fleeting C0012628 Discrete subaortic stenosis HSDN C3887638 Failure to thrive in infant C2930866 Ramos arroyo clark syndrome MalaCards C0033774 Skin pruritus C0162568 Erythropoietic protoporphyria OrphaNet|HPO|UMLS C0010038 Corneal opacity disorder C0268496 Kramer syndrome OrphaNet|MalaCards C2984058 Have pain C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C3274924 Have been coughing C0003507 Aortic valve stenosis HSDN C3539895 Pelvic pain occurs with bowel movement C1299262 Sarcoma - category (morphologic abnormality) HSDN C4084774 Have weight loss C0013336 Dwarfism HSDN C3641756 Have diarrhea C1855652 Fetus small for gestational age HSDN C1963071 Back pain adverse event C0027819 Neuroblastoma HSDN C0003862 Pain joint C1861481 Stickler syndrome, type 3 OrphaNet|HPO|UMLS C0030232 Color loss C0028840 Ocular hypertension HSDN C3898969 Have been vomiting C0162869 Aneurysm, ruptured HSDN C0005745 Blepharoptosis C2931720 Fronto-facio-nasal dysostosis OrphaNet|MalaCards C0973461 Dysphasia C0242387 Mandibulofacial dysostosis MalaCards|HPO C0027497 Queasy C0275911 Tuberculosis of intestines MalaCards C3539893 Pelvic pain occurs with intercourse C0206622 Adenomyoma HSDN C4084774 Have weight loss C1546602 Specimen source codes - diverticulum HSDN C0018772 Deafness C0032285 Pneumonia HSDN C0015469 Facial paralysis C0024530 Malaria HSDN C1963281 Vomiting adverse event C0021228 Variability of individual responses HSDN C0019209 Large liver C1850363 Niemann-pick disease, nova scotian type HPO C0522224 Palsied C0003803 Arnold chiari malformation HSDN C0009806 Constipate C0035372 Rett syndrome MalaCards|HSDN|HPO|UMLS C2024893 Cardiovascular surgery result: fatigue C0013481 Ebstein anomaly OrphaNet|HPO|MalaCards C0030486 Extremity paralysis, lower C0031154 Peritonitis HSDN C4085210 Usual severity pain C0028796 Dermatitis, occupational HSDN C4084802 Usual severity diarrhea C0009663 Condylomata acuminata HSDN C0008031 Pain chest C0919267 Ovarian neoplasm HSDN C0004604 Pain back C0023092 Lassa fever MalaCards C1963091 Diarrhea adverse event C0020875 Ileal diseases HSDN C0041657 Consciousness loss C0018801 Heart failure HSDN C3539023 Pelvic pain increasing in frequency C0017638 Glioma HSDN C0036396 Sciatica C0025299 Meningocele HSDN C1963170 Hypothermia adverse event C0006285 Bronchopneumonia HSDN C1557397 Adverse event associated with pain C0424318 Bullied HSDN C4082202 Sleep quality question C3888109 Acromelalgia hereditary MalaCards C0004134 Dyssynergia C0751785 Unverricht-lundborg syndrome OrphaNet|HSDN|UMLS|HPO|MalaCards C0037771 Paraparesis spastic C0038826 Superinfection HSDN C3641756 Have diarrhea C0017563 Gingival diseases HSDN C0557874 Global developmental delay C3715051 Craniosynostosis 3 MalaCards C0042963 Symptoms vomiting C0032987 Ectopic pregnancy HSDN C2048468 Inability to impregnate C1507149 Partial chromosome y deletion OrphaNet|HPO|MalaCards C0031911 Pigment deposition C0859920 Hair follicle neoplasm MalaCards C3146279 Coma C1832903 Migraine, sporadic hemiplegic HPO C0349588 Stature short C1859711 Arthrogryposis multiplex congenita with whistling face OrphaNet|MalaCards C0013378 Dysgensia C1442903 Exostoses HSDN C0557874 Global developmental delay C0796279 Carnevale syndrome MalaCards|HPO C2911645 Weight loss adverse event C0029410 Osteoarthritis of hip HSDN C0027796 Neuralgias C1963198 Pancreatitis adverse event HSDN C4049602 Hyperactivity C0265202 Seckel syndrome MalaCards|HPO C1850830 Exercise-induced muscle pain C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C0241210 Speaking delay C3280799 Cutis laxa, autosomal recessive, type iiib MalaCards C0413252 Hypothermia due to exposure C0023895 Liver diseases HSDN C0023014 Developmental disorder language C0032914 Pre-eclampsia HSDN C4085211 Pain distress question C0035923 German measles vaccine HSDN C3887873 Hearing loss C0027441 Nasopharyngitis HSDN C0042571 Vertigo subjective C0338437 Neurocysticercosis HSDN C1557397 Adverse event associated with pain C0014856 Esophageal fistula HSDN C0518179 Change voice C1527340 Abnormal voice UMLS C4085211 Pain distress question C0006105 Brain abscess HSDN C3665386 Abnormal vision C1854065 Late-onset retinal degeneration (disorder) HPO C0494475 Seizure generalized tonic clonic C0796110 Pallister syndrome 1 MalaCards C0009421 Comatose C0021832 Intestinal diseases, parasitic HSDN C0728710 Pupil constriction observed C0009363 Congenital ocular coloboma (disorder) HSDN C2984058 Have pain C0013808 Electroconvulsive therapy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033968 Psychotherapeutic technique HSDN C0007758 Cerebellar ataxia C1846492 Spinocerebellar ataxia, autosomal recessive 4 MalaCards C2132198 Abnormal blistering of the skin C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C0478124 Other unspecif skin change C0549660 Other skin disorders UMLS C0007758 Cerebellar ataxia C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0018991 Paralysis one side of body C1556682 Adverse event associated with infection HSDN C0021359 Infertility C0342384 Idiopathic hypogonadotropic hypogonadism HPO C4084776 Weight loss C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C2096293 Ent surgical result ear vertigo C0030297 Pancreatic neoplasm HSDN C0237326 Defecation pain C0265499 49,xxxxy chromosomal anomaly OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0003516 Aortopulmonary septal defect HSDN C0042571 Vertigo subjective C0002351 Altitude sickness HSDN C1557397 Adverse event associated with pain C1862939 Amyotrophic lateral sclerosis 1 MalaCards C1527344 Dysphonia C0376527 Neoplasm, skull base HSDN C0085636 Light sensitivity C0038826 Superinfection HSDN C0013595 Eczematous dermatitis C1849236 Severe combined immunodeficiency, atypical HPO C3641756 Have diarrhea C0021334 Infectious bovine rhinotracheitis HSDN C0043094 Weight gain C0005941 Bone diseases, developmental HSDN C1549543 Administration method - pain C0031149 Peritoneal neoplasms HSDN C0042963 Symptoms vomiting C1299919 Enteric coccidiosis HSDN C4084774 Have weight loss C0039231 Tachycardia HSDN C0030552 Paralysis partial C0026896 Myasthenia gravis OrphaNet|MalaCards C0013362 Dysarthrias C0268247 Niemann-pick disease, type d MalaCards|HPO C0518090 Frequency of pain question C0036982 Shock, hemorrhagic HSDN C0030200 Intractable pain C0033970 Time limited psychotherapy HSDN C2911647 Weight gain adverse event C0032310 Pneumonia, viral HSDN C0013362 Dysarthrias C3280452 Spinocerebellar ataxia, autosomal recessive 12 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0027625 Circulating neoplastic cells HSDN C0013421 Dystonia C0796200 Wieacker-wolff syndrome MalaCards C4084767 Bothered by vomiting C1706377 Memory device component HSDN C0019079 Bloody sputum C0025064 Mediastinitis HSDN C2919142 Short stature adverse event C1861922 Campomelic dysplasia OrphaNet|HPO|MalaCards C0018775 Hearing loss bilateral C0035920 Rubella HSDN C0004604 Pain back C0015408 Eye injury HSDN C2919142 Short stature adverse event C3280054 Geleophysic dysplasia 2 MalaCards C0003862 Pain joint C2748507 Interleukin 1 receptor antagonist deficiency HPO|UMLS C0151311 Cranial nerve palsy C0853240 Mobius ii syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0034194 Pyloric stenosis HSDN C4085661 Usual severity nausea C0340629 Aortic aneurysm without mention of rupture nos HSDN C0518090 Frequency of pain question C0221056 Adult type dermatomyositis HSDN C0010520 Skin cyanosis C0011608 Dermatitis herpetiformis HSDN C2237041 Shox gene with short stature C3697269 15q24 microdeletion OrphaNet|HPO C0349588 Stature short C0162530 Porphyria, erythropoietic HPO C0030193 Sense of pain C0010403 Cryoglobulinemia HSDN C0151818 Opisthotonos C0751667 Canavan disease, juvenile MalaCards C0237326 Defecation pain C0153653 Malignant tumor of parathyroid gland MalaCards C4085210 Usual severity pain C0340464 Heartbeats ectopic HSDN C3665492 Pigmentations C0153535 Malignant melanoma of skin of upper limb MalaCards C1963091 Diarrhea adverse event C0036875 Disorders of sex development HSDN C0518090 Frequency of pain question C0024419 Waldenstrom macroglobulinemia HSDN C0000737 Abdomen pain C3273071 Bile duct mucinous cystic neoplasm with high grade intraepithelial neoplasia UMLS C1557397 Adverse event associated with pain C0242994 Hantavirus infections HSDN C0242936 Center pain C0152177 Trigeminal neuropathy HSDN C4084724 Usual severity constipation C1963215 Pneumothorax adverse event HSDN C0002170 Alopecia disorders C0002726 Amyloidosis MalaCards C4085210 Usual severity pain C0238461 Anaplastic thyroid carcinoma OrphaNet C0398650 Idiopathic thrombocytopenia purpura C0004623 Bacterial infections HSDN C3463815 Feel fatigue C0026269 Mitral valve stenosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0039106 Pigmented villonodular synovitis HSDN C0018926 Emesis bloody C0017168 Gastroesophageal reflux disease HSDN C0038002 Spleen enlargement C0004364 Autoimmune diseases MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0022610 Kernicterus HSDN C0000727 Abdomen acute C0014356 Enterocolitis HSDN C0009460 Communication impairment C0038273 Stereotypic movement disorder HSDN C0241210 Speaking delay C3281138 Chromosome 17q12 deletion syndrome MalaCards C3887873 Hearing loss C0752180 Bacterial cns infection HSDN C0022346 Yellow skin C2673914 Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive MalaCards C3539896 Pelvic pain occurs with urination C1458155 Mammary neoplasms HSDN C0033774 Skin pruritus C0038986 Sweat gland diseases HSDN C0424755 Fever symptoms C0025229 Melioidosis DiseaseOntology|MalaCards C0522224 Palsied C0013080 Down syndrome HSDN C4085211 Pain distress question C0006818 Campylobacter infection HSDN C0036572 Convulsion C0268465 Phenylketonuria ii MalaCards|HPO|UMLS C0037763 Spasm C0009240 Cognition HSDN C0005745 Blepharoptosis C1857576 Contractures, congenital, torticollis, and malignant hyperthermia MalaCards C0085631 Abnormal excitement C0026769 Multiple sclerosis HSDN C0018772 Deafness C0265965 Dyskeratosis congenita MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C1864997 Majeed syndrome MalaCards|HPO C0398650 Idiopathic thrombocytopenia purpura C0032197 Platelet storage pool deficiency HSDN C0085650 Purpura fulminans C0748226 Radial neuropathy HSDN C0015469 Facial paralysis C0001418 Adenocarcinoma HSDN C0018772 Deafness C0221026 X-linked agammaglobulinemia HPO C0013362 Dysarthrias C0023374 Lesch-nyhan syndrome MalaCards|HSDN|HPO C3641756 Have diarrhea C0022865 Obstetric labor complications HSDN C0557874 Global developmental delay C3151058 Hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase HPO C4085211 Pain distress question C1258104 Diffuse scleroderma HSDN C0220982 Keto acidosis C1833102 Diabetes mellitus, permanent neonatal, with neurologic features HPO C0010520 Skin cyanosis C0032319 Pneumopericardium HSDN C0003811 Cardiac rhythm disturbance C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C2096293 Ent surgical result ear vertigo C0005935 Bone conduction HSDN C4084775 Usual severity weight loss C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0000737 Abdomen pain C0026916 Mycobacterium avium-intracellulare infection HSDN C1963281 Vomiting adverse event C0162526 Aids-related opportunistic infections HSDN C0022346 Yellow skin C0024299 Lymphoma HSDN C1963087 Constipation adverse event C3203358 Hypoventilation MalaCards C2096293 Ent surgical result ear vertigo C2674004 Von hippel-lindau syndrome, modifiers of HPO C2024893 Cardiovascular surgery result: fatigue C0796561 Melanoma vaccines HSDN C0009421 Comatose C0919267 Ovarian neoplasm HSDN C0009421 Comatose C0023890 Liver cirrhosis HSDN C4020887 Photodysphoria C3887937 Cone dystrophy 5, x-linked MalaCards C0008031 Pain chest C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C4085549 Dizziness C1527336 Sjogren's syndrome HSDN C4085222 Nausea C0022890 Labyrinthine disorder HSDN C0033774 Skin pruritus C0406298 Subacute prurigo UMLS C0023530 Leukopenia C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO C4084897 Sleep disturbance subordinate domain C1857844 Williams-beuren region duplication syndrome MalaCards C0015230 Exanthem C1276074 Adult atopic dermatitis recurrent in adult life UMLS C0001825 Agraphia C0030569 Secondary parkinson disease HSDN C4050613 Anxiety C0342443 Adrenal cushing's syndrome MalaCards C2984058 Have pain C0027430 Nasal polyps HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010414 Infection by cryptococcus neoformans HSDN C4085862 Bothered by nausea C2586211 Thrombosis of blood vessel HSDN C0013604 Edematous C0949690 Spondylarthritis HSDN C0151686 Growth retardation C1854988 Molybdenum cofactor deficiency, complementation group a HPO C2919142 Short stature adverse event C0265313 Weill-marchesani syndrome OrphaNet|HPO|MalaCards C0027796 Neuralgias C0038019 Spondylosis HSDN C0030552 Paralysis partial C3813607 Infantile gastroesophageal reflux HSDN C0020673 Hypothermia (central) (local) C1096660 Ehlers-danlos syndrome type ix MalaCards C0009421 Comatose C0018939 Hematological disease HSDN C2984058 Have pain C0340629 Aortic aneurysm without mention of rupture nos HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040409 Tongue diseases HSDN C4084766 Vomiting C0028432 Nose diseases HSDN C0036572 Convulsion C1546602 Specimen source codes - diverticulum HSDN C0041657 Consciousness loss C0038538 Effusion subdural HSDN C0860603 Anxiety symptom C2242987 Benign mastocytoma MalaCards C4084775 Usual severity weight loss C0400822 Colitis, lymphocytic HSDN C0015970 Fever unknown origin C0037274 Dermatologic disorders HSDN C0007758 Cerebellar ataxia C0085409 Polyendocrinopathies, autoimmune HSDN C0013604 Edematous C0010073 Coronary artery vasospasm HSDN C0007758 Cerebellar ataxia C0085292 Stiff-person syndrome HSDN C0522224 Palsied C0031887 Picornaviridae infections HSDN C1549543 Administration method - pain C0497580 Condylomata acuminata in men HSDN C4084768 Usual severity vomiting C0007137 Squamous cell carcinoma HSDN C0011991 Loose stools C0030354 Papilloma HSDN C0033377 Caudal displacement C1838562 Khalifa graham syndrome MalaCards C0037771 Paraparesis spastic C2117411 X-ray of toe: syndactyly HSDN C0042024 Urine incontinence C0006413 Burkitt lymphoma HSDN C0007758 Cerebellar ataxia C0002871 Anemia HSDN C1279888 Proteinuria of undiagnosed cause C1857342 Deafness, cochlear, with myopia and intellectual impairment HPO C0023380 Lethargy C0917890 Pineocytoma MalaCards C1963087 Constipation adverse event C0018133 Graft-vs-host disease HSDN C0033377 Caudal displacement C1850864 Familial congenital muscular dystrophy with gonadal dysgenesis OrphaNet|MalaCards C0162298 Stiffness joints C0432291 Mandibuloacral dysostosis HPO|UMLS C2315100 Pediatric failure to thrive C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C4084774 Have weight loss C0035242 Respiratory tract diseases HSDN C1279511 Malarial pigment deposition C1704421 Skin pigmentation disorder UMLS C0026826 High muscle tone C1857568 Cortical blindness, retardation, and postaxial polydactyly OrphaNet|MalaCards C0027498 Nausea vomiting C0004239 Atrial flutter UMLS C0012833 Dizzy C0023371 Lermoyez syndrome UMLS C3815497 Cough C1306577 Dies patient HSDN C2203646 Jaundice C0038356 Stomach neoplasms HSDN C3539895 Pelvic pain occurs with bowel movement C0242669 Placenta retained HSDN C0349588 Stature short C0268547 Argininosuccinic aciduria OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C2963140 Arteriovenous fistula in use with two needles HSDN C1963170 Hypothermia adverse event C1510412 Pseudoaneurysm HSDN C0009792 Consciousness disorder C1527348 Brain hypoxia HSDN C0030193 Sense of pain C1134719 Invasive ductal breast carcinoma HSDN|UMLS C4085317 Diarrhea frequency C0015397 Disorder of eye HSDN C1557397 Adverse event associated with pain C1963211 Pericarditis adverse event HSDN C0004604 Pain back C2240378 Cleft palate on exam HSDN C0015672 Decreased energy C0024523 Malabsorption syndrome HSDN C0233794 Memory impaired C1858680 Familial encephalopathy with neuroserpin inclusion bodies MalaCards C0038999 Swelling C0001427 Adenoiditis, nos MalaCards C0019209 Large liver C2700553 Omenn syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C3495801 Granulomatosis with polyangiitis HSDN C0013421 Dystonia C0268621 Hepatic methionine adenosyltransferase deficiency HPO C3829611 Nausea frequency C0025007 Measles HSDN C0015672 Decreased energy C1963137 Hydrocephalus adverse event HSDN C1963071 Back pain adverse event C0007784 Cerebral hemisphere hemorrhage HSDN C0018775 Hearing loss bilateral C1384672 Hpt gene HSDN C0005779 Clotting C0398650 Immune thrombocytopenic purpura MalaCards C0015970 Fever unknown origin C0162557 Liver failure, acute HSDN C4085210 Usual severity pain C0002989 Epithelioid hemangioma of skin HSDN C3146279 Coma C0006434 Burn injury HSDN C0700590 Diaphoresis excessive C2931735 Epidermolytic palmoplantar keratoderma vorner type OrphaNet|HPO|MalaCards C0162298 Stiffness joints C0265245 Nager syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0101725 Receptor for advanced glycation endproducts HSDN C0013404 Respiratory difficulty C0023869 Lithiasis HSDN C0013404 Respiratory difficulty C0206733 Strawberry nevus of skin HSDN C2127284 Urinary incontinence without sensory awareness C0042024 Urinary incontinence UMLS C4085317 Diarrhea frequency C0041971 Tumor urethra HSDN C4084776 Weight loss C1552527 Clinic / center - developmental disabilities HSDN C1000483 Genus anemia C0079294 Epidermolysis bullosa dystrophica MalaCards C0232943 Metromenorrhagia C0342442 Acth-dependent cushing's syndrome OrphaNet C0026884 Muteness C1136249 Mental retardation, x-linked HSDN C1963093 Dizziness adverse event C0008350 Cholelithiasis HSDN C0012833 Dizzy C0035435 Rheumatism HSDN C4084769 Vomiting frequency C1970820 Fabry disease, cardiac variant HPO C1963091 Diarrhea adverse event C0008533 Hemophilia b HSDN C3887638 Failure to thrive in infant C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C2024878 Cardiovascular surgery result: dyspnea C4049994 Insulin resistance measurement HSDN C0013395 Indigestion C0026946 Mycoses HSDN C0000737 Abdomen pain C0006264 Bronchial neoplasms HSDN C0231218 Malaise generalized C3273047 Perihilar bile duct carcinoma UMLS C2128817 Single skin crust C0242787 Malignant neoplasm of male breast MalaCards C0013362 Dysarthrias C0162671 Melas syndrome MalaCards|HSDN|HPO C0013421 Dystonia C0011849 Diabetes mellitus HSDN C3274924 Have been coughing C0302148 Blood clot HSDN C3463815 Feel fatigue C0242343 Panhypopituitarism OrphaNet|HPO|MalaCards C0231528 Muscle pain generalized C0027073 Myofascial pain syndromes HSDN C0023380 Lethargy C0011311 Dengue fever MalaCards C3146279 Coma C0023702 Injury lightning HSDN C0085631 Abnormal excitement C0035435 Rheumatism HSDN C0349489 Fetal hypoxia C0086468 Injuries, prenatal HSDN C0497406 Over weight C0028756 Obesity, morbid UMLS C0013362 Dysarthrias C0796160 Mental retardation, x-linked, snyder-robinson type HPO C0009806 Constipate C0009475 Community mental health service HSDN C0009792 Consciousness disorder C0751865 Alcohol-induced disorders, nervous system HSDN C0242843 Sweating sickness C1145628 Autonomic nervous system disorders HSDN C2242996 Tingling C1394891 Intrinsic factor deficiency MalaCards|HPO C0751295 Memory loss or impairment C1836148 Supranuclear palsy, progressive, 2 MalaCards C0042755 Virilisation C3810814 Myocardial infarction ecg assessment HSDN C0424853 Finger mass C0685154 Neoplasm - soft tissue types blood vessel malignant upper limb finger secondary UMLS C4085210 Usual severity pain C0027664 Neoplasms, muscle tissue HSDN C4085862 Bothered by nausea C2827407 Infectious otitis media HSDN C4084768 Usual severity vomiting C0085277 Munchausen by proxy syndrome HSDN C0030193 Sense of pain C0020507 Hyperplasia HSDN C0023380 Lethargy C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO|UMLS C0036659 Sensation disorder C0010267 Cranial nerve neoplasms HSDN C0036572 Convulsion C0275148 Poisoning of animal by plant HSDN C0034150 Skin purpura C1842763 Spondyloenchondrodysplasia with immune dysregulation MalaCards|HPO C0015469 Facial paralysis C0014038 Encephalitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0031485 Phenylketonurias HSDN C1549543 Administration method - pain C0282612 Prostatic intraepithelial neoplasias HSDN C4085317 Diarrhea frequency C0040843 Treponemal disease HSDN C0751837 Gait ataxic C0020179 Huntington disease MalaCards|HPO C4084774 Have weight loss C0860603 Anxiety symptoms HSDN C4084773 Bothered by weight gain C0152156 Dystocia HSDN C0013595 Eczematous dermatitis C1853392 Interleukin 2 receptor, alpha, deficiency of MalaCards|HPO C0700590 Diaphoresis excessive C1835650 Focal palmoplantar and gingival hyperkeratosis syndrome OrphaNet|MalaCards C0851578 Disorder sleep C0001818 Agoraphobia HSDN C0043094 Weight gain C0600519 Ventricular remodeling HSDN C4084774 Have weight loss C0007682 Cns disorder HSDN C0042963 Symptoms vomiting C0011168 Deglutition disorders HSDN C0008031 Pain chest C0344423 Atrial flutter by ecg finding HSDN C1963093 Dizziness adverse event C0033860 Psoriasis HSDN C0020578 Hyperventilate C0020626 Hypoparathyroidism HSDN C0008031 Pain chest C1866552 Paragangliomas 2 (disorder) MalaCards C4042891 Sleep wake disorders C3542413 Cdisc adas-cog - comprehension HSDN C3463815 Feel fatigue C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0476273 Distress respiratory C1849554 Lymphangiectasia, pulmonary, congenital OrphaNet|MalaCards C0043094 Weight gain C0040583 Tracheal stenosis HSDN C2096293 Ent surgical result ear vertigo C0003467 Anxiety HSDN C4085211 Pain distress question C0019621 Histiocytosis, langerhans-cell HSDN C0018681 Headache, cephalalgia C0032371 Poliomyelitis MalaCards|HSDN C3815497 Cough C0206703 Carcinoma, giant cell HSDN C4085210 Usual severity pain C0037974 Spirochaetales infections HSDN C0424755 Fever symptoms C1444838 Chronic arthritis of juvenile onset OrphaNet C1304408 Urticarial vasculitis C1290834 Acute skin disorder UMLS C0015230 Exanthem C1623452 Barmah forest virus infection MalaCards C0040822 D tremors C0032965 Pregnancy complications, infectious HSDN C0027796 Neuralgias C0024141 Lupus erythematosus, systemic HSDN C0575090 Disorder equilibrium C1846790 Joubert syndrome 4 (disorder) MalaCards C0035078 Failure kidney C0155127 Familial amyloid polyneuropathy, type v MalaCards C0027066 Myoclonic jerking C0595812 Fistula route HSDN C0012833 Dizzy C0020676 Hypothyroidism HSDN C0004134 Dyssynergia C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C2237041 Shox gene with short stature C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C0037316 Not enough sleeping C0027765 Nervous system disorder HSDN C3829611 Nausea frequency C0023895 Liver diseases HSDN C0018681 Headache, cephalalgia C0009917 Contracture HSDN C0235153 Sensory hallucination C0033800 Pseudoglioma MalaCards C4084767 Bothered by vomiting C0021432 Infratentorial neoplasms HSDN C0026838 Spasticity muscle C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0008521 Choroid diseases HSDN C1549543 Administration method - pain C0013386 Dyskinesia, drug-induced HSDN C1961131 Cough adverse event C0037304 Skull fracture HSDN C0009792 Consciousness disorder C0025284 Meningeal neoplasms HSDN C0030486 Extremity paralysis, lower C0040715 Chromosomal translocation HSDN C4084784 Diarrhea C1623041 Breast-fed HSDN C0042928 Paralysis vocal cord C0039144 Syringomyelia HSDN C0003862 Pain joint C3809369 Paroxysmal nocturnal hemoglobinuria 2 MalaCards|UMLS C0151889 Reflexes tendon increased C2677903 Mental retardation and microcephaly with pontine and cerebellar hypoplasia MalaCards|HPO C0426579 Anorexia symptom C0001430 Adenoma HSDN C0700078 Deep tendon reflex decrease C4015307 Perrault syndrome 5 MalaCards C4084767 Bothered by vomiting C0007134 Renal cell carcinoma HSDN C0021359 Infertility C2751811 Spermatogenic failure 7 MalaCards C0042963 Symptoms vomiting C0035439 Rheumatic heart disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1285666 Drinking behavior HSDN C0040034 Thrombocytopenia C1856492 Gaucher disease, type iiib HPO C0026838 Spasticity muscle C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO|UMLS C0030193 Sense of pain C0009088 Cluster headache UMLS C0349588 Stature short C0796137 3c syndrome OrphaNet|HPO|MalaCards C0002622 Amnesias C0027407 Narcotherapy HSDN C0037316 Not enough sleeping C0015671 Father HSDN C2024893 Cardiovascular surgery result: fatigue C0003504 Aortic valve insufficiency HSDN C0027497 Queasy C0034885 Rectal neoplasms HSDN C4085222 Nausea C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0038002 Spleen enlargement C4015542 Nephronophthisis 19 MalaCards C4020887 Photodysphoria C1852438 Cataract, coppock-like MalaCards|HPO C0018681 Headache, cephalalgia C0751291 Desmoplastic medulloblastoma MalaCards|UMLS C0016199 Pain flank C0040015 Thrombasthenia HSDN C0036572 Convulsion C4039032 Status epilepticus due to generalised idiopathic epilepsy UMLS C4084784 Diarrhea C0997768 Glaucoma HSDN C0242936 Center pain C1368355 Synostosis malformation HSDN C4084775 Usual severity weight loss C0035335 Retinoblastoma HSDN C4084767 Bothered by vomiting C0305062 Tetanus toxoids HSDN C2315100 Pediatric failure to thrive C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C4084774 Have weight loss C0023241 Legionnaires' disease HSDN C0007859 Pain neck C0039483 Giant cell arteritis HSDN C0231218 Malaise generalized C1519321 Signet ring cell intrahepatic cholangiocarcinoma UMLS C1963252 Tremor adverse event C0032963 Pregnancy complications, cardiovascular HSDN C0002962 Angina C0243013 Base learn problems HSDN C0003862 Pain joint C0158360 Fibromatosis plantar OrphaNet|MalaCards C0424755 Fever symptoms C0002871 Anemia HSDN C0036572 Convulsion C0002382 Alveolar bone loss HSDN C0242936 Center pain C0011630 Dermatomycoses HSDN C0009792 Consciousness disorder C0238156 Hematoma, subdural, intracranial HSDN C0031911 Pigment deposition C1852020 Malattia leventinese MalaCards C0004134 Dyssynergia C0242422 Parkinsonian disorders HSDN C0039070 Collapse fleeting C0242350 Erectile dysfunction HSDN C0036659 Sensation disorder C0020458 Hyperhidrosis disorder HSDN C0151786 Weakness muscle C1849322 Sandhoff disease, infantile type HPO C0019825 Voice hoarseness C0040136 Thyroid neoplasm HSDN C3665347 Vision impaired C3554001 Peroxisome biogenesis disorder 11b MalaCards C0233844 Awkwardness C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0151786 Weakness muscle C4225364 Myasthenic syndrome, congenital, 18 UMLS C0162298 Stiffness joints C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C0030200 Intractable pain C0027073 Myofascial pain syndromes HSDN C0020580 Decreased sensation C1962963 Osteoporosis adverse event HSDN C3641756 Have diarrhea C0162531 Hereditary coproporphyria HPO C0003862 Pain joint C3711158 Metatropic dwarfism, type ii MalaCards C0043094 Weight gain C0039590 Testicular neoplasms HSDN C4085210 Usual severity pain C0018023 Nodular goiter HSDN C0015676 Mental fatigue C0460137 Push down or depress HSDN C0018991 Paralysis one side of body C0917800 Epilepsy, myoclonic, infantile MalaCards C4085661 Usual severity nausea C1456781 Benign melanocytic nevus HSDN C1557397 Adverse event associated with pain C2984302 Leishmaniasis infection pathway HSDN C3463815 Feel fatigue C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0011991 Loose stools C1527311 Brain edema HSDN C3641756 Have diarrhea C0037051 Behavior illness HSDN C1850830 Exercise-induced muscle pain C0268123 Muscle amp deaminase deficiency MalaCards C0013421 Dystonia C1835916 Aicardi-goutieres syndrome 3 MalaCards|HPO C4085549 Dizziness C0007781 Intracranial embolism and thrombosis HSDN C0000737 Abdomen pain C0149573 Structure of posterior inferior cerebellar artery HSDN C0349588 Stature short C0266209 Congenital dilatation of colon MalaCards C0237326 Defecation pain C0235387 Porphyria type syndrome OrphaNet C4085317 Diarrhea frequency C0206754 Neuroendocrine tumors HSDN C0011991 Loose stools C1535939 Pneumocystis jiroveci pneumonia HSDN|UMLS C0413252 Hypothermia due to exposure C0018824 Heart valve disease HSDN C4085211 Pain distress question C0038987 Sweat gland neoplasms HSDN C0557874 Global developmental delay C1843366 Niemann-pick disease, type c2 MalaCards|HPO C0270948 Neurogenic muscular atrophy C2751325 46,xy gonadal dysgenesis, partial, with minifascicular neuropathy OrphaNet|HPO C0018772 Deafness C0268140 Xeroderma pigmentosum, group f HPO C0007859 Pain neck C0038454 Cerebrovascular accident UMLS C0020505 Excessive eating C0017075 Ganglioneuroma MalaCards C1963091 Diarrhea adverse event C0021603 Sleep initiation and maintenance disorders HSDN C0043094 Weight gain C0020732 Iatrogenic disease HSDN C0086565 Liver function abnormal C0431693 Renal cysts and diabetes syndrome MalaCards|HPO C0751495 Seizure focal C1845235 Heterotopia, periventricular, ehlers-danlos variant OrphaNet|HPO C4084775 Usual severity weight loss C0024809 Marijuana abuse HSDN C0021359 Infertility C0748400 Rh disease MalaCards C0151889 Reflexes tendon increased C0796028 Ataxia, fatal x-linked, with deafness and loss of vision MalaCards|HPO C0424755 Fever symptoms C3163843 Chondrosarcoma of bone HSDN C0151786 Weakness muscle C0080174 Spina bifida occulta HSDN C0278230 Retinal sign, nos C0035317 Retinal hemorrhage UMLS C0027498 Nausea vomiting C0267204 Drug-induced nausea and vomiting, nos UMLS C0010200 Cough symptom C0033975 Psychotic disorders HSDN C4084768 Usual severity vomiting C0040559 Toxoplasmosis in animals HSDN C1145670 Failure respiratory C1266101 Thymic epithelial tumor OrphaNet C0042025 Urinary incontinence stress C4085311 Depression - recess HSDN C4085222 Nausea C0860603 Anxiety symptoms HSDN C0003862 Pain joint C1851124 Desmoid disease, hereditary MalaCards C4084727 Cough frequency C0028758 Bonding HSDN C0242936 Center pain C0085409 Polyendocrinopathies, autoimmune HSDN C0020580 Decreased sensation C0376175 Bell palsy HSDN C1963063 Anorexia adverse event C0085399 Ehrlichiosis HSDN C4085549 Dizziness C0011849 Diabetes mellitus HSDN C0015672 Decreased energy C1832998 Epiphyseal dysplasia, multiple, 3 MalaCards C0013604 Edematous C0005686 Urinary bladder diseases HSDN C0020578 Hyperventilate C0003864 Arthritis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0517960 Neurological status: consciousness HSDN C0022346 Yellow skin C0012979 Canine disease HSDN C4085211 Pain distress question C0042749 Viremia HSDN C2024893 Cardiovascular surgery result: fatigue C0013504 Echinococcosis, hepatic HSDN C4085210 Usual severity pain C0027902 Neuropsychological diagnosis HSDN C0003079 Pupillary inequality C0043253 Trauma blunt HSDN C0002962 Angina C3714644 Thymus neoplasms HSDN C0002622 Amnesias C0010068 Coronary heart disease HSDN C0235698 Abdom.distension, gaseous C0810319 Other and unspecified gastrointestinal disorders UMLS C0004134 Dyssynergia C1333989 Familial meningioma MalaCards C0424755 Fever symptoms C0037937 Spine injury HSDN C0750394 Wbc low C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0423721 Painful arms and moving fingers C0393901 Disorders of spinal neurones manifest by hyperactivity UMLS C0008031 Pain chest C0035243 Respiratory tract infections HSDN C0917816 Deficiency mental C1857242 Rhizomelic chondrodysplasia punctata, type 2 HPO C0000737 Abdomen pain C0004030 Aspergillosis HSDN C0042755 Virilisation C2748895 Ovotesticular disorders of sex development HSDN C0242936 Center pain C0037221 Situs inversus HSDN C0030193 Sense of pain C0206488 Peer review, health care HSDN C0518090 Frequency of pain question C1552052 Religious affiliation - meditation HSDN C0030193 Sense of pain C0013336 Dwarfism HSDN C0749856 Upper extremity weakness acute C0741197 Aphasia acute UMLS C0042963 Symptoms vomiting C0025007 Measles HSDN C0013404 Respiratory difficulty C0010356 Cross infection HSDN C0042963 Symptoms vomiting C0795956 Chylomicron retention disease OrphaNet|UMLS|HPO|MalaCards C0004134 Dyssynergia C0205710 Alpers syndrome (disorder) OrphaNet|UMLS|HPO|MalaCards C2919142 Short stature adverse event C1861923 Acampomelic campomelic dysplasia MalaCards C3887873 Hearing loss C0031154 Peritonitis HSDN C3463815 Feel fatigue C2986550 Pituicytoma MalaCards C0036572 Convulsion C1845539 Autism, x-linked, susceptibility to, 2 (finding) HPO C3274924 Have been coughing C0041315 Tuberculosis, laryngeal HSDN C0151786 Weakness muscle C0021051 Immunologic deficiency syndromes HSDN C0700078 Deep tendon reflex decrease C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C0003862 Pain joint C0151744 Myocardial ischemia HSDN C3539890 Pelvic pain causes awakening at night C0023903 Liver neoplasms HSDN C1963086 Confusion adverse event C0043251 Wounds and injuries HSDN C4084767 Bothered by vomiting C0242383 Age related macular degeneration HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0039747 Thecoma HSDN C2875630 Eyelid retraction unspecified eye, unspecified lid C0015397 Disorder of eye UMLS C4084768 Usual severity vomiting C0268569 Intermittent maple syrup urine disease HPO C4084725 Usual severity cough C4015016 Ciliary dyskinesia, primary, 30 MalaCards C0011206 Delirium acute C2063866 Depressive disorder, treatment-resistant HSDN C0917816 Deficiency mental C0795833 Kleefstra syndrome HPO C0005745 Blepharoptosis C0032001 Pituitary apoplexy MalaCards C1963071 Back pain adverse event C0022976 Animal gait disorder HSDN C1963247 Ventricular tachycardia adverse event C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards|HPO C4084776 Weight loss C0812393 Cancer patients and suicide and depression HSDN C0018784 Deafness sensorineural C0268136 Xeroderma pigmentosum, group b HPO C4084727 Cough frequency C0266284 Lingual thyroid HSDN C0349489 Fetal hypoxia C1548578 Location characteristic id - smoking HSDN C2911645 Weight loss adverse event C0919691 Anastomotic leaks HSDN C3808046 Breathing dysregulation C3203358 Hypoventilation MalaCards C0030552 Paralysis partial C0018801 Heart failure HSDN C2024878 Cardiovascular surgery result: dyspnea C2706915 Language:-:point in time:^patient:- HSDN C0023380 Lethargy C4049644 Depression HSDN C4085211 Pain distress question C0035412 Rhabdomyosarcoma HSDN C1565249 Limitation, mobility C1414899 Gaa gene HSDN C4084766 Vomiting C1527258 Infantile paralysis MalaCards C2237041 Shox gene with short stature C1837481 Spondyloepimetaphyseal dysplasia, matrilin-3 related OrphaNet C2024893 Cardiovascular surgery result: fatigue C0265201 De sanctis-cacchione syndrome MalaCards C0917816 Deficiency mental C1858562 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 MalaCards|HPO C0241210 Speaking delay C3810282 Chromosome 5q12 deletion syndrome MalaCards C0027066 Myoclonic jerking C1834570 Myoclonic dystonia HPO|UMLS C2315100 Pediatric failure to thrive C3150787 Chromosome 17q21.31 duplication syndrome MalaCards C4085317 Diarrhea frequency C0021400 Influenza HSDN C4085317 Diarrhea frequency C0400827 Proctitis radiation MalaCards C0007758 Cerebellar ataxia C0020758 Congenital ichthyosis HSDN C0085636 Light sensitivity C1852438 Cataract, coppock-like MalaCards|HPO C4084773 Bothered by weight gain C0022116 Ischemia HSDN C0012833 Dizzy C0011265 Presenile dementia HSDN C0030193 Sense of pain C0010417 Cryptorchidism HSDN C2029884 Hearing loss by exam C0010823 Cytomegalovirus infections HSDN C0339780 Syncopal vertigo C0155523 Disorders of the vestibular system and vertiginous syndromes UMLS C0015402 Hemorrhage eye C0023968 Loiasis HSDN C0026858 Musculoskeletal pain C0205770 Choroid plexus papilloma HSDN C0004134 Dyssynergia C0007137 Squamous cell carcinoma HSDN C0233514 Behavior abnormal C0268225 Aspartylglucosaminuria MalaCards C0019079 Bloody sputum C0027668 Neoplasms, vascular tissue HSDN C1384666 Decreased hearing C0265338 Coffin-siris syndrome OrphaNet|HPO C4084724 Usual severity constipation C0025162 Megacolon toxic HSDN C0007758 Cerebellar ataxia C0009650 Conditions eyelid HSDN C4084767 Bothered by vomiting C1456865 Ureteral calculi HSDN C0020455 Hypergammaglobulinemia C0023480 Leukemia, myelomonocytic, chronic HSDN C0026821 Cramp C0014457 Eosinophilia HSDN C0151786 Weakness muscle C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C1963087 Constipation adverse event C0021400 Influenza HSDN C1963281 Vomiting adverse event C0033375 Prolactinoma OrphaNet|HPO|MalaCards C4084773 Bothered by weight gain C0037579 Soft tissue neoplasms HSDN C3898969 Have been vomiting C1546635 Specimen source codes - fistula HSDN C0151825 Ostalgia C0152441 Madelung deformity OrphaNet|MalaCards C1963137 Hydrocephalus adverse event C1835820 Holoprosencephaly 7 HPO C0000737 Abdomen pain C0035309 Retinal diseases HSDN C0917816 Deficiency mental C1850442 Ceroid lipofuscinosis, neuronal, 5 MalaCards|HPO C0012833 Dizzy C0029118 Opportunistic infections HSDN C0151889 Reflexes tendon increased C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C0000731 Abdomen distention C1856113 Mowat-wilson syndrome MalaCards|HPO C0727671 Red cross toothache drops C1963198 Pancreatitis adverse event HSDN C0349588 Stature short C1848912 Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage MalaCards C0010520 Skin cyanosis C0017563 Gingival diseases HSDN C4084773 Bothered by weight gain C4041080 Neurocognitive disorders HSDN C0002962 Angina C0039144 Syringomyelia HSDN C4084774 Have weight loss C0162832 Apc HSDN C0015732 Feces incontinence C3495554 Homocarnosinase deficiency MalaCards C0413252 Hypothermia due to exposure C0008325 Cholecystitis HSDN C0031911 Pigment deposition C0017636 Glioblastoma MalaCards C0040822 D tremors C0009207 Cockayne syndrome OrphaNet|MalaCards C0007758 Cerebellar ataxia C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C3641753 Lacks appetite C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0023380 Lethargy C0520679 Sleep apnea, obstructive HSDN C0036572 Convulsion C1547044 Kind of quantity - smell HSDN C0518090 Frequency of pain question C0024689 Mandibular diseases HSDN C1963249 Tinnitus adverse event C0011119 Decompression sickness HSDN C2315100 Pediatric failure to thrive C3146297 Study of behavior during childhood HSDN C0018772 Deafness C0040336 Tobacco use disorder HSDN C0000737 Abdomen pain C0206754 Neuroendocrine tumors HSDN C3463815 Feel fatigue C1963198 Pancreatitis adverse event HSDN C4084769 Vomiting frequency C0042781 Visceral myopathy MalaCards C0518090 Frequency of pain question C1336753 Thyroid lymphoma MalaCards C1557397 Adverse event associated with pain C0752242 Limitus, hallux HSDN C0851578 Disorder sleep C0003838 Arterial occlusive diseases HSDN C1963093 Dizziness adverse event C0087012 Ataxia, spinocerebellar HSDN C4084768 Usual severity vomiting C1720922 Respiratory aspiration HSDN C1963180 Neck pain adverse event C0027122 Myositis ossificans HSDN C0026838 Spasticity muscle C1839040 Leber optic atrophy and dystonia UMLS C2984058 Have pain C3873472 Vulvovaginal gingival syndrome MalaCards C0018681 Headache, cephalalgia C1136033 Cutaneous mastocytosis MalaCards C2132198 Abnormal blistering of the skin C0079298 Epidermolysis bullosa simplex OrphaNet|MalaCards C4084723 Constipation C0037313 Sleep HSDN C3146279 Coma C0018939 Hematological disease HSDN C1557397 Adverse event associated with pain C0040583 Tracheal stenosis HSDN C1279888 Proteinuria of undiagnosed cause C0007781 Intracranial embolism and thrombosis HSDN C0234518 Speech slurred C1527231 Adrenomyeloneuropathy MalaCards|HPO C0009806 Constipate C0005586 Bipolar disorder HSDN C0035078 Failure kidney C1848813 Thyrocerebral-retinal syndrome MalaCards C0151786 Weakness muscle C3813607 Infantile gastroesophageal reflux HSDN C0042571 Vertigo subjective C1963083 Cholecystitis adverse event HSDN C0339251 Blood pigmentation of cornea C0549567 Pigmentation disorders UMLS C2919142 Short stature adverse event C1843418 Niemann-pick disease, type f HPO C4085210 Usual severity pain C0030312 Pancytopenia HSDN C2203646 Jaundice C0039231 Tachycardia HSDN C2129378 Elbow is 'frozen' C0016059 Fibrosis UMLS C1963180 Neck pain adverse event C0034530 Injury radiation HSDN C1962972 Proteinuria adverse event C0032269 Pneumococcal infections HSDN C0454644 Delayed language development C1854630 Growth deficiency and mental retardation with facial dysmorphism MalaCards|HPO C2096293 Ent surgical result ear vertigo C0518449 Control of hip fracture risk HSDN C1557397 Adverse event associated with pain C0025281 Meniere disease HSDN C3539892 Pelvic pain in front C0684743 Malignant neoplasm of muscle HSDN C4084767 Bothered by vomiting C1253937 Pericardial effusion HSDN C4084767 Bothered by vomiting C1856401 Etfa deficiencies HPO C0232466 Feeding difficulty C0349653 Congenital disorder of glycosylation type 1a MalaCards C0023380 Lethargy C3150973 Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degeneration and progressive polyneuropathy type) MalaCards|HPO|UMLS C1962972 Proteinuria adverse event C0018794 Heart block HSDN C1963087 Constipation adverse event C0265246 Townes syndrome OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0795887 Chromosome xp21 deletion syndrome MalaCards C4084767 Bothered by vomiting C0040156 Thyrotoxicosis HSDN C4084788 Have dizziness C0428953 Ecg infarction myocardial HSDN C0030975 Disorders perception C0014544 Epilepsy HSDN C0518090 Frequency of pain question C0013289 Duodenal diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0037744 Perceptual spatial orientation HSDN C4042891 Sleep wake disorders C0027831 Neurofibromatosis 1 HSDN C0018784 Deafness sensorineural C1851710 Lateral meningocele syndrome MalaCards C3887873 Hearing loss C0013446 Acquired ear deformities HSDN C0151786 Weakness muscle C1579931 Depressed - symptom HSDN C4084802 Usual severity diarrhea C0024668 Mammary neoplasms, experimental HSDN C0018784 Deafness sensorineural C0391889 Bony union HSDN C0040485 Wryneck C0080179 Vertebra fracture HSDN C0023012 Delay language C2936862 Bardet-biedl syndrome 1 (disorder) MalaCards C0242936 Center pain C0018133 Graft-vs-host disease HSDN C2984058 Have pain C0265334 Pachyonychia congenita HSDN C4084784 Diarrhea C1257915 Intestinal polyposis HSDN C0037316 Not enough sleeping C0007131 Non-small cell lung carcinoma HSDN C0557874 Global developmental delay C0574085 3-methylglutaconic aciduria type 4 OrphaNet|MalaCards C0042963 Symptoms vomiting C0032963 Pregnancy complications, cardiovascular HSDN C1963281 Vomiting adverse event C0008350 Cholelithiasis HSDN C0857305 Thrombocytopenia purpura C0026946 Mycoses HSDN C0017181 Gastrointestinal bleed C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0018681 Headache, cephalalgia C0023051 Laryngeal diseases HSDN C1553190 Icterus - observation C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards C0242936 Center pain C0033046 Premenstrual syndrome HSDN C1549543 Administration method - pain C0030472 Paraneoplastic syndromes HSDN C3665347 Vision impaired C1848922 Hexosaminidase alpha-subunit deficiency (variant b) OrphaNet|MalaCards C1963071 Back pain adverse event C0009241 Cognition disorders HSDN C4084723 Constipation C0559260 Congenital scoliosis HSDN C3146279 Coma C1546847 Entity name part type - family HSDN C1090821 Sepsis C0006666 Calciphylaxes OrphaNet|MalaCards C0042571 Vertigo subjective C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0577564 Mass of lymphoreticular structure C0686582 Primary malignant neoplasm of bone marrow UMLS C2984058 Have pain C0376378 Barre lieou syndrome HSDN C0221263 Cafe au lait spot C0017566 Gingival hyperplasia HSDN C0019521 Hiccoughs C0030508 Parasomnia HSDN C0241137 Skin pallor C0031511 Pheochromocytoma MalaCards|HSDN C2237041 Shox gene with short stature C1844918 Branchial arch syndrome, x-linked OrphaNet|MalaCards C4085222 Nausea C0038941 Incisional infection HSDN C0015469 Facial paralysis C0020540 Malignant hypertension HSDN C0812426 Kidney problem C1561643 Chronic kidney diseases UMLS C0018681 Headache, cephalalgia C1848814 Thymoma, familial MalaCards C0023380 Lethargy C0006147 Breast fed HSDN C0033774 Skin pruritus C3273134 Extrahepatic bile duct cystadenocarcinoma UMLS C0917816 Deficiency mental C0342286 Woodhouse sakati syndrome OrphaNet|HPO|MalaCards C0000727 Abdomen acute C0001418 Adenocarcinoma HSDN C0595939 Stillborn C1848600 Vater association with hydrocephalus HPO C0497247 Blood pressure elevation C0344490 Sacral agenesis HPO C0013456 Pain ear C0014591 Epistaxis HSDN C0700590 Diaphoresis excessive C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C0016199 Pain flank C0003857 Congenital arteriovenous malformation HSDN C0036659 Sensation disorder C0700327 Clinical findings relating to memory HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014335 Enteritis HSDN C0557874 Global developmental delay C0162635 Angelman syndrome MalaCards|HPO C0026858 Musculoskeletal pain C0162819 Skin diseases, vascular HSDN C0013404 Respiratory difficulty C1711276 Carcinosarcoma of lung UMLS C0010038 Corneal opacity disorder C0086647 Mucopolysaccharidosis type iiia MalaCards C4042891 Sleep wake disorders C0000768 Congenital abnormality HSDN C0003862 Pain joint C0033860 Psoriasis HSDN C0221166 Paraparesis C0162636 Infection, spirurida HSDN C0518090 Frequency of pain question C0029882 Otitis media HSDN C0151686 Growth retardation C2675512 Diamond-blackfan anemia 7 MalaCards C0009421 Comatose C1555914 Psychologist - psychotherapy, group HSDN C0037317 Sleep disturbance C1384514 Conn syndrome MalaCards C0850758 Pain pelvic C0085222 Psoas muscle abscess HSDN C4084727 Cough frequency C0008325 Cholecystitis HSDN C4049602 Hyperactivity C1845366 Mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance MalaCards|HPO C0036572 Convulsion C0000735 Abdominal neoplasms HSDN C0457004 Adolescent striae C0333641 Atrophic UMLS C0018681 Headache, cephalalgia C0032816 Post-concussion headache UMLS C4085661 Usual severity nausea C3489413 Lipomatosis, multiple HSDN C0039070 Collapse fleeting C0340629 Aortic aneurysm without mention of rupture nos HSDN C1000483 Genus anemia C0175703 Thrombocytopenia-absent radius syndrome MalaCards|HPO C0042940 Disorder of voice C4049644 Depression HSDN C0034150 Skin purpura C0796126 Aicardi-goutieres syndrome 1 HPO C0022346 Yellow skin C3554004 Pbd13a MalaCards C0424755 Fever symptoms C0003838 Arterial occlusive diseases HSDN C0020305 Fetal edema C0004623 Bacterial infections HSDN C3665347 Vision impaired C2930866 Ramos arroyo clark syndrome MalaCards C0030232 Color loss C1961099 Precursor t-cell lymphoblastic leukemia-lymphoma HSDN C0030193 Sense of pain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C2315100 Pediatric failure to thrive C0175701 Aarskog syndrome MalaCards|HPO C0011991 Loose stools C0002063 Alkalosis HSDN C0344307 Analgesia C2931817 Chromosome 2q37 deletion syndrome MalaCards C0042798 Vision dim C0016563 Form perception HSDN C0518090 Frequency of pain question C0004940 Behavioral science HSDN C3541349 Syncope C0021051 Immunologic deficiency syndromes HSDN C0040264 Ear ringing sound C0271097 Usher syndrome MalaCards C0242936 Center pain C2985290 Fetal alcohol spectrum disorders HSDN C0424755 Fever symptoms C0034067 Pulmonary emphysema HSDN C4085211 Pain distress question C0085207 Gestational diabetes HSDN C2984058 Have pain C0020655 Hypothalamic diseases HSDN C2919142 Short stature adverse event C1856492 Gaucher disease, type iiib HPO C0473129 Diarrhea after git surgery C1290807 Diarrheal disorder UMLS C0472514 Edema uvula C0553694 Oropharyngeal disorders UMLS C0005745 Blepharoptosis C0268532 Deficiency of prolidase MalaCards|HPO C0413252 Hypothermia due to exposure C0025202 Melanoma HSDN C2242996 Tingling C1075202 Paronychia HSDN C3641756 Have diarrhea C2937358 Cerebral hemorrhage HSDN C3274924 Have been coughing C2242987 Benign mastocytoma MalaCards C4084726 Distress cough C0524799 Hyperlucent lung HSDN C3829611 Nausea frequency C0034088 Pulmonary valve insufficiency HSDN C0020580 Decreased sensation C0006635 Cadmium poisoning HSDN C0036572 Convulsion C0006012 Borderline personality disorder HSDN C0041657 Consciousness loss C0009241 Cognition disorders HSDN C2203646 Jaundice C1963215 Pneumothorax adverse event HSDN C0019825 Voice hoarseness C0024299 Lymphoma UMLS C0042025 Urinary incontinence stress C0013473 Eating disorders HSDN C0018681 Headache, cephalalgia C3264032 Menstrual migraine, intractable UMLS C0009421 Comatose C3888018 Congenital hyperinsulinism MalaCards C0009421 Comatose C0042345 Varicosity HSDN C0241137 Skin pallor C1005359 Pica pica bird HSDN C0426576 Gastrointestinal symptom C2957359 Influenza a with gastrointestinal manifestations UMLS C0018808 Murmur C0265425 9p partial monosomy syndrome MalaCards C4084726 Distress cough C0031090 Periodontal diseases HSDN C0037771 Paraparesis spastic C0020541 Hypertension, portal HSDN C0853986 Lymphocytes decreased C0152094 Cellular immunodeficiency with abnormal immunoglobulin deficiency MalaCards C0009676 Confusion state C0021368 Inflammation HSDN C4084784 Diarrhea C0268124 Adenosine deaminase deficiency MalaCards C4085211 Pain distress question C0027086 Myoma HSDN C0917816 Deficiency mental C0431375 Classical lissencephaly MalaCards C0270948 Neurogenic muscular atrophy C2930869 Pelvic dysplasia associated with arthrogrypotic changes in the lower extremities OrphaNet|MalaCards C0007758 Cerebellar ataxia C2931925 Abetalipoproteinemia neuropathy MalaCards C1557397 Adverse event associated with pain C0033785 Pseudarthrosis HSDN C1384666 Decreased hearing C1844865 Charcot-marie-tooth disease, x-linked recessive, 3 (disorder) OrphaNet C0014724 Burping C0439840 Reflex motion descriptor HSDN C2096293 Ent surgical result ear vertigo C0021799 Interprofessional relations HSDN C0221166 Paraparesis C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0242936 Center pain C0235032 Neurotoxicity syndromes HSDN C0028738 Nystagmus C4014261 Spinocerebellar ataxia, autosomal recessive 16 MalaCards C0020580 Decreased sensation C0376527 Neoplasm, skull base HSDN C4049644 Depression C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 HPO C0241210 Speaking delay C1306856 Megaloblastic anemia due to inborn errors of metabolism MalaCards C2984058 Have pain C0034884 Rectal fistula HSDN C3539889 Pelvic pain increasing in severity C0037286 Skin neoplasms HSDN C0030193 Sense of pain C0020503 Hyperparathyroidism, secondary HSDN C0024032 Birth weight subnormal C0574108 Glycerol kinase deficiency - isolated MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C1963138 Hypertension adverse event HSDN C3829611 Nausea frequency C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C4084784 Diarrhea C0699744 Infection of ear HSDN C4085222 Nausea C0026771 Trauma multiple HSDN C0016927 Gag reflex C0032343 Poisoning HSDN C1145670 Failure respiratory C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0030756 Pediculosis HSDN C0030193 Sense of pain C0856761 Budd-chiari syndrome HSDN C0795692 Lactate blood increased C0003962 Ascites HSDN C0023014 Developmental disorder language C2015933 Outcomes otolaryngology hearing HSDN C1069915 Vertigo C0027663 Neoplasms, multiple primary HSDN C1963170 Hypothermia adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0242670 Chronic vegetative state C0028850 Ocular motility disorders HSDN C0024031 Back pain lower back C1552262 Nurse practitioner - family HSDN C4085317 Diarrhea frequency C0242172 Pelvic inflammatory disease HSDN C4084723 Constipation C0220981 Metabolic acidosis HSDN C0016382 Cutaneous vascular engorgement C0010073 Coronary artery vasospasm HSDN C4049644 Depression C1846058 Lubs x-linked mental retardation syndrome HPO C4085210 Usual severity pain C0040896 Trichinellosis HSDN C1963091 Diarrhea adverse event C3489413 Lipomatosis, multiple HSDN C2024878 Cardiovascular surgery result: dyspnea C1963067 Atrial fibrillation adverse event HSDN C4084788 Have dizziness C1968848 Epilepsy, familial mesial temporal lobe MalaCards C3898969 Have been vomiting C0014836 Escherichia coli infections HSDN C4084727 Cough frequency C0006288 Bronchopulmonary sequestration HSDN C2024878 Cardiovascular surgery result: dyspnea C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C0917816 Deficiency mental C0340951 Erythrogenesis imperfecta MalaCards C0030193 Sense of pain C0023891 Liver cirrhosis, alcoholic HSDN C0518090 Frequency of pain question C0019034 Hemoglobin sc disease MalaCards|HSDN C0015672 Decreased energy C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C4084773 Bothered by weight gain C0021361 Female infertility HSDN C1963281 Vomiting adverse event C0206644 Histiocytoma, benign fibrous HSDN C0013404 Respiratory difficulty C0015695 Fatty liver HSDN C0037316 Not enough sleeping C1522133 High cholesterol level HSDN C0018681 Headache, cephalalgia C3899662 Childhood fibrillary astrocytoma UMLS C4084774 Have weight loss C0041296 Tuberculosis OrphaNet|HPO C0018775 Hearing loss bilateral C4085311 Depression - recess HSDN C0042963 Symptoms vomiting C1263846 Attention deficit hyperactivity disorder HSDN C2025995 Cellulitis C0020497 Cortical congenital hyperostosis OrphaNet|HPO|MalaCards C0027066 Myoclonic jerking C0270853 Myoclonic epilepsy, juvenile UMLS C0011991 Loose stools C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C0151825 Ostalgia C0017205 Gaucher disease OrphaNet|MalaCards C0085631 Abnormal excitement C0376298 Consensus HSDN C2024893 Cardiovascular surgery result: fatigue C0010068 Coronary heart disease HSDN C0020538 Hbp C1865872 Nephronophthisis 2 HPO C1549543 Administration method - pain C1366464 F9 gene HSDN C1963087 Constipation adverse event C0717360 Disease lyme vaccine HSDN C0221166 Paraparesis C0079744 Diffuse large b-cell lymphoma HSDN C0002962 Angina C1720777 Functional laterality HSDN C3541349 Syncope C0042133 Uterine fibroids HSDN C4084775 Usual severity weight loss C0042373 Vascular diseases HSDN C1384666 Decreased hearing C3888029 Deafness, autosomal dominant 54 MalaCards C0004604 Pain back C3539923 Cdisc adas-cog - orientation summary score HSDN C1963274 Vasculitis adverse event C2931873 Juvenile cranial arteritis MalaCards C0013362 Dysarthrias C2677565 Amyotrophic lateral sclerosis 10 (disorder) HPO C2984058 Have pain C0017919 Glycogen storage disease HSDN C4084775 Usual severity weight loss C0016658 Fracture bone HSDN C3665492 Pigmentations C1334557 Brain neoplasms, adult, malignant MalaCards C4085210 Usual severity pain C1959600 Obscure african cardiomyopathy HSDN C0917816 Deficiency mental C0080024 Piebaldism HPO C0037763 Spasm C0023055 Laryngeal neoplasm HSDN C2911647 Weight gain adverse event C0005941 Bone diseases, developmental HSDN C0427055 Face weakness C0410204 Myopathy, centronuclear, autosomal recessive HPO|UMLS C0003862 Pain joint C0494043 Streptobacillosis MalaCards C0007814 Cerebrospinal fluid otorrhea C0043254 Injuries penetrating HSDN C0000737 Abdomen pain C0001969 Alcoholic intoxication HSDN C0518090 Frequency of pain question C0025427 Mercury poisoning HSDN C0042940 Disorder of voice C2004491 Cicatrix HSDN C0013421 Dystonia C0242287 Isaacs syndrome HSDN C0035229 Respiratory function impaired C1861922 Campomelic dysplasia OrphaNet|HPO|MalaCards C4084776 Weight loss C0010346 Crohn disease MalaCards C0042798 Vision dim C1845069 Albinism, ocular, with late-onset sensorineural deafness (disorder) OrphaNet C0557874 Global developmental delay C0265863 Dextrocardia, isolated MalaCards C0026821 Cramp C0011581 Depressive disorder HSDN C4049644 Depression C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C4084769 Vomiting frequency C0007137 Squamous cell carcinoma HSDN C4084802 Usual severity diarrhea C0008066 Child behavior disorders HSDN C3163620 Hypotension adverse event C2930957 Hantavirosis MalaCards C0151786 Weakness muscle C0221065 Subacute combined degeneration HSDN C0039070 Collapse fleeting C0277919 Postthrombotic syndrome UMLS C0151786 Weakness muscle C0751813 Chronic brain injury HSDN C1549543 Administration method - pain C0024961 Injuries maxillofacial HSDN C0497406 Over weight C0021390 Inflammatory bowel diseases HSDN C0030193 Sense of pain C0037774 Spatial behavior HSDN C1549543 Administration method - pain C0206708 Cervical intraepithelial neoplasia HSDN C0018772 Deafness C0038015 Spondyloepiphyseal dysplasia MalaCards C4085317 Diarrhea frequency C0032914 Pre-eclampsia HSDN C0013404 Respiratory difficulty C1334363 Large cell lung neuroendocrine carcinoma UMLS C4084774 Have weight loss C0220981 Metabolic acidosis HSDN C3641756 Have diarrhea C0007124 Noninfiltrating intraductal carcinoma HSDN C4085211 Pain distress question C0040559 Toxoplasmosis in animals HSDN C0022346 Yellow skin C0035335 Retinoblastoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2706915 Language:-:point in time:^patient:- HSDN C4085862 Bothered by nausea C0342443 Adrenal cushing's syndrome HSDN C0036572 Convulsion C0021818 Intervertebral disk displacement HSDN C0003862 Pain joint C0158484 Acquired genu valgum HSDN C3463815 Feel fatigue C2937287 Hematolysis HSDN C1963274 Vasculitis adverse event C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0042373 Vascular diseases HSDN C0027497 Queasy C1332243 Adenocarcinoma of ampulla of vater UMLS C2911645 Weight loss adverse event C0027819 Neuroblastoma MalaCards|HSDN C0008031 Pain chest C0036690 Septicemia HSDN C0242936 Center pain C0013289 Duodenal diseases HSDN C0000737 Abdomen pain C1963134 Hemorrhoids adverse event HSDN C0018772 Deafness C0007762 Cerebellar neoplasms HSDN C0011991 Loose stools C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C1962972 Proteinuria adverse event C0023487 Acute promyelocytic leukemia HSDN C4084725 Usual severity cough C0016045 Fibroma HSDN C4084784 Diarrhea C0020676 Hypothyroidism HSDN C0349588 Stature short C0265313 Weill-marchesani syndrome OrphaNet|HPO|MalaCards C0520909 Ponv C0021890 Intraoperative complications HSDN C0028738 Nystagmus C0282525 Adrenoleukodystrophy, neonatal OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0014068 Encephalomalacia HSDN C0497406 Over weight C0022661 Kidney failure, chronic HSDN C4085661 Usual severity nausea C0016057 Fibrosarcoma HSDN C0036572 Convulsion C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii OrphaNet|HPO|MalaCards C0019825 Voice hoarseness C0020627 Hypopharyngeal neoplasms HSDN C0151786 Weakness muscle C0027126 Myotonic dystrophy MalaCards|HPO C2237041 Shox gene with short stature C3492944 Lentiginosis profusa MalaCards C0030486 Extremity paralysis, lower C0020295 Hydronephrosis HSDN C0578055 Pain of head and neck region C1868714 Eagle syndrome UMLS C4085862 Bothered by nausea C0152164 Cyclical vomiting syndrome (disorder) MalaCards C1557397 Adverse event associated with pain C0025268 Multiple endocrine neoplasia type 2a HSDN C0015672 Decreased energy C1709572 Pleural desmoplastic mesothelioma UMLS C0424755 Fever symptoms C0025149 Medulloblastoma HSDN C1963281 Vomiting adverse event C0002994 Angioedema HSDN C2203646 Jaundice C0034530 Injury radiation HSDN C2237041 Shox gene with short stature C0268579 Propionic acidemia HPO C4084775 Usual severity weight loss C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C1557397 Adverse event associated with pain C0162869 Aneurysm, ruptured HSDN C3815497 Cough C0403447 Chronic kidney insufficiency HSDN C0030193 Sense of pain C0007140 Carcinosarcoma HSDN C0027066 Myoclonic jerking C0007134 Renal cell carcinoma HSDN C0042963 Symptoms vomiting C0062527 Hepatitis b vaccine HSDN C0024031 Back pain lower back C0023676 Life style HSDN C0018772 Deafness C2675512 Diamond-blackfan anemia 7 MalaCards C0013404 Respiratory difficulty C0854983 Lung adenocarcinoma, recurrent UMLS C4084802 Usual severity diarrhea C0042512 Ventricular outflow obstruction HSDN C4084776 Weight loss C0085111 Ankle injury HSDN C0036572 Convulsion C0034212 Pyoderma HSDN C0013404 Respiratory difficulty C0041952 Uerterolithiasis HSDN C3274924 Have been coughing C1090821 Sepsis (invertebrate) HSDN C0151786 Weakness muscle C0376329 New variant creutzfeldt-jakob disease MalaCards C1963252 Tremor adverse event C0346303 Thyrotroph adenoma OrphaNet|MalaCards C4084775 Usual severity weight loss C0022865 Obstetric labor complications HSDN C0007758 Cerebellar ataxia C1136043 Acoustic schwannoma, bilateral HPO C0030975 Disorders perception C0003811 Cardiac arrhythmia HSDN C0236000 Jaw bone pain C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C4084784 Diarrhea C0027794 Neural tube defects HSDN C0020673 Hypothermia (central) (local) C0796561 Melanoma vaccines HSDN C0013404 Respiratory difficulty C0039538 Teratoma HSDN C0518090 Frequency of pain question C3827868 Tachycardia by ecg finding HSDN C1963091 Diarrhea adverse event C0029342 Orthomyxoviridae infections HSDN C0917816 Deficiency mental C1836916 Posterior column ataxia with retinitis pigmentosa HPO C3641755 Have constipation C0011581 Depressive disorder HSDN C0042940 Disorder of voice C1458155 Mammary neoplasms HSDN C3829611 Nausea frequency C0038828 Arteriomesenteric duodenal ileus HSDN C4084802 Usual severity diarrhea C0001727 Afferent loop syndrome HSDN C1384666 Decreased hearing C1510455 Acrocephalosyndactylia MalaCards|HSDN C0010520 Skin cyanosis C1548578 Location characteristic id - smoking HSDN C0030552 Paralysis partial C0024790 Paroxysmal nocturnal hemoglobinuria MalaCards|HPO C0271215 Blindness legal C2931258 Amaurosis congenita of leber, type 1 MalaCards|HPO C0040822 D tremors C1836485 Charcot-marie-tooth disease, axonal, type 2a2 (disorder) HPO C0009421 Comatose C0242723 Parasitemia HSDN C0018926 Emesis bloody C1832529 Hereditary hemorrhagic telangiectasia-related pulmonary arterial hypertension HPO C2984058 Have pain C0043515 Zollinger-ellison syndrome HSDN C0242936 Center pain C0027859 Acoustic neuroma HSDN C4085210 Usual severity pain C0034040 Puerperal disorders HSDN C0030975 Disorders perception C0597109 Nurse's role HSDN C3539023 Pelvic pain increasing in frequency C0016542 Foreign body HSDN C0041105 Jaw spasm C0009677 Congenital macroglossia HSDN C2029884 Hearing loss by exam C0001193 Apert syndrome MalaCards|HSDN C0023380 Lethargy C0010481 Cushing syndrome HPO C0427055 Face weakness C0265301 Sclerosteosis OrphaNet|HPO|MalaCards C0032617 High urine output C0020456 Hyperglycemia HSDN|UMLS C0013362 Dysarthrias C1836899 Spastic paraplegia 27, autosomal recessive (disorder) MalaCards C0030486 Extremity paralysis, lower C0036357 Psychology, schizophrenic HSDN C0020673 Hypothermia (central) (local) C0460137 Push down or depress HSDN C0042755 Virilisation C1257809 Steroid metabolism, inborn errors HSDN C0011206 Delirium acute C0004941 Behavioral symptoms HSDN C0917816 Deficiency mental C0085131 Gangliosidosis gm1 HPO C0019825 Voice hoarseness C1837218 Cleft palate, isolated HSDN C0015469 Facial paralysis C0021818 Intervertebral disk displacement HSDN C1963170 Hypothermia adverse event C0009319 Colitis HSDN C0037763 Spasm C0018564 Hand deformities HSDN C0030552 Paralysis partial C0010054 Coronary arteriosclerosis HSDN C1836296 Lower extremity weakness C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO|UMLS C0004604 Pain back C0158298 Other and unspecified back disorders UMLS C4085222 Nausea C0038356 Stomach neoplasms HSDN C1971624 Appetite absent C0011581 Depressive disorder HSDN C3539022 Pelvic pain decreasing in severity C0023895 Liver diseases HSDN C3163620 Hypotension adverse event C1852529 Corticosteroid-binding globulin deficiency MalaCards|HPO C4042891 Sleep wake disorders C0025500 Mesothelioma HSDN C0424755 Fever symptoms C0007282 Carotid stenosis HSDN C0035078 Failure kidney C0376359 Groenblad-strandberg syndrome MalaCards|HPO C0004604 Pain back C0035066 Renal artery obstruction HSDN C0013595 Eczematous dermatitis C4015214 Autoimmune lymphoproliferative syndrome, type v MalaCards C0013428 Painful urination C0271001 Siderosis of eye HSDN C3641755 Have constipation C0013364 Dysautonomia, familial HPO C4085210 Usual severity pain C0853697 Neutrophil count decreased HSDN C0018681 Headache, cephalalgia C0242188 Spider bites HSDN C0231712 Gait waddling C1842160 Myopathy, myosin storage (disorder) HPO|UMLS C0270327 Bed wetting C1858392 Nephronophthisis 3 MalaCards|HPO C0003862 Pain joint C0276119 Q-fever pneumonia MalaCards C0023380 Lethargy C3810404 Carbonic anhydrase va deficiency, hyperammonemia due to UMLS C0231528 Muscle pain generalized C1833373 Inclusion body myopathy, autosomal recessive MalaCards C0015469 Facial paralysis C1623209 Okihiro syndrome MalaCards|HPO C0234146 Absent reflex C1834336 Nemaline myopathy 3 HPO C0012569 Double vision C1836474 Spinocerebellar ataxia, autosomal recessive 7 MalaCards C4084773 Bothered by weight gain C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C4084775 Usual severity weight loss C0024215 Lymphangiectasis, intestinal MalaCards|HSDN C4084775 Usual severity weight loss C0040156 Thyrotoxicosis MalaCards|HSDN C2919142 Short stature adverse event C1862103 Brachydactyly type c MalaCards|HPO C0036572 Convulsion C0008625 Chromosome aberrations HSDN C0033377 Caudal displacement C0878675 Erdheim-chester disease MalaCards C3815497 Cough C0009404 Colorectal neoplasms HSDN C0019079 Bloody sputum C3539615 Nci ctep sdc gestational trophoblastic disease sub-category terminology HSDN C4085641 Level of joint pain C0152063 Streptobacillus moniliformis infection DiseaseOntology|MalaCards C3641755 Have constipation C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0022346 Yellow skin C0033700 Infection proteus HSDN C0012833 Dizzy C0014544 Epilepsy HSDN C1069915 Vertigo C0268595 Glutaric aciduria, type 1 HPO C0033377 Caudal displacement C1969053 Joubert syndrome 7 MalaCards|HPO C0030975 Disorders perception C0042797 Monocular vision HSDN C1145670 Failure respiratory C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C0413252 Hypothermia due to exposure C2586211 Thrombosis of blood vessel HSDN C0018681 Headache, cephalalgia C1332188 Adult brain medulloblastoma UMLS C0030193 Sense of pain C1336039 Sphenoid sinus squamous cell carcinoma UMLS C3898969 Have been vomiting C0020649 Hypotension HSDN C4084774 Have weight loss C1266101 Thymic epithelial tumor OrphaNet C3829611 Nausea frequency C0038463 Strongyloides infection HSDN C3873641 Pain due to varicose veins of leg C4047625 Pain co-occurrent and due to varicose veins of left leg UMLS C4050613 Anxiety C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0349588 Stature short C0004775 Bartter disease OrphaNet|MalaCards C0007758 Cerebellar ataxia C0026470 Monoclonal gammopathy of undetermined significance HSDN C1069915 Vertigo C0004933 Behavior modification technique HSDN C0012833 Dizzy C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0237326 Defecation pain C0042075 Urologic diseases MalaCards C0018808 Murmur C0027821 Syndrome effort HSDN C0020580 Decreased sensation C0022578 Keratoconus HSDN C0036396 Sciatica C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084802 Usual severity diarrhea C0085092 Parenting behavior HSDN C3274924 Have been coughing C0221390 Non-bacterial thrombotic endocarditis HSDN C0518090 Frequency of pain question C0039980 Chest injury HSDN C2024893 Cardiovascular surgery result: fatigue C0085399 Ehrlichiosis DiseaseOntology|MalaCards C1962972 Proteinuria adverse event C0021831 Intestinal diseases HSDN C0518090 Frequency of pain question C0024312 Lymphopenia HSDN C0018524 Hallucinate C0001807 Aggressive behavior HSDN C1279888 Proteinuria of undiagnosed cause C0268626 Juvenile nephropathic cystinosis (disorder) HPO C1963252 Tremor adverse event C0038273 Stereotypic movement disorder HSDN C0009792 Consciousness disorder C0012644 Animal disease models HSDN C2032396 Pelvic pain on the right C3887532 Ulceration HSDN C4084724 Usual severity constipation C0029106 Opisthorchiasis DiseaseOntology C0042928 Paralysis vocal cord C0038661 Suicide HSDN C4084773 Bothered by weight gain C0039336 Gustatory sense HSDN C0085632 Listlessness C0039373 Tay-sachs disease MalaCards|HPO|UMLS C0427055 Face weakness C2749128 Myopathy, congenital, with fiber-type disproportion, x-linked UMLS C0014591 Bleeding nose C1260903 Dysfibrinogenemia MalaCards C0020505 Excessive eating C0005891 Bodies image HSDN C2911645 Weight loss adverse event C0079731 B-cell lymphomas HSDN C3641756 Have diarrhea C1855849 Bartter syndrome, antenatal , type 2 HPO C0036659 Sensation disorder C0022661 Kidney failure, chronic HSDN C0151686 Growth retardation C3150796 Nephronophthisis 11 MalaCards|HPO C2911645 Weight loss adverse event C0600041 Infective cystitis HSDN C2032395 Pelvic pain on the left C0022865 Obstetric labor complications HSDN C1000483 Genus anemia C1847319 Paraganglioma and gastric stromal sarcoma MalaCards C4085317 Diarrhea frequency C0007130 Mucinous adenocarcinoma HSDN C0042928 Paralysis vocal cord C1963067 Atrial fibrillation adverse event HSDN C0028738 Nystagmus C1855466 Hypomagnesemia 5, renal, with ocular involvement OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0279651 Gallbladder adenocarcinoma UMLS C1557397 Adverse event associated with pain C0010267 Cranial nerve neoplasms HSDN C1963093 Dizziness adverse event C2827407 Infectious otitis media HSDN C0042940 Disorder of voice C0018671 Head and neck neoplasms HSDN C0011206 Delirium acute C0035243 Respiratory tract infections HSDN C0027066 Myoclonic jerking C0026650 Movement disorders UMLS C0015300 Ocular proptosis C0270972 Cornelia de lange syndrome HPO C3898969 Have been vomiting C0032460 Polycystic ovary syndrome HSDN C3539895 Pelvic pain occurs with bowel movement C0015558 Fallopian tube neoplasms HSDN C0036572 Convulsion C0039336 Gustatory sense HSDN C0424755 Fever symptoms C1998095 Epizootic lymphangitis MalaCards C3714552 Strength decreased C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C1962972 Proteinuria adverse event C0149514 Bronchitis acute HSDN C0557874 Global developmental delay C2931286 Mosaic variegated aneuplody microcephaly syndrome OrphaNet|HPO|MalaCards C0151908 Dry skin C0011175 Dehydration UMLS C0042571 Vertigo subjective C0004275 Attitude health HSDN C0030193 Sense of pain C0037299 Skin ulcer HSDN C1963281 Vomiting adverse event C1527348 Brain hypoxia HSDN C1963065 Apnea adverse event C0038454 Cerebrovascular accident HSDN C0013404 Respiratory difficulty C0345946 Epidermoid carcinoma of trachea UMLS C0030552 Paralysis partial C0005779 Blood coagulation disorders HSDN C4085210 Usual severity pain C0033324 Prognathism HSDN C1963252 Tremor adverse event C0014070 Encephalomyelitis HSDN C1963184 Nystagmus adverse event C1848745 Oliver-mcfarlane syndrome MalaCards|HPO C1090821 Sepsis C0263979 Myositis, purulent MalaCards C2024878 Cardiovascular surgery result: dyspnea C0348018 Projections HSDN C2984058 Have pain C0026528 Moral code HSDN C0151686 Growth retardation C1836330 Erythrokeratodermia variabilis 3 (disorder) HPO C4085862 Bothered by nausea C0032131 Plasmacytoma HSDN C4084766 Vomiting C0038013 Ankylosing spondylitis HSDN C0233844 Awkwardness C1836474 Spinocerebellar ataxia, autosomal recessive 7 MalaCards C0020455 Hypergammaglobulinemia C0027659 Neoplasms, experimental HSDN C0015468 Face pain C0030470 Paranasal sinus neoplasms HSDN C2237041 Shox gene with short stature C0010495 Cutis laxa OrphaNet|MalaCards C4085862 Bothered by nausea C0016510 Foot diseases HSDN C0557874 Global developmental delay C1864186 Cdags syndrome OrphaNet|MalaCards C0013395 Indigestion C0011389 Dental plaque HSDN C0009676 Confusion state C0037274 Dermatologic disorders HSDN C2936821 Spinal cerebrospinal fluid leak C0010267 Cranial nerve neoplasms HSDN C0454644 Delayed language development C1845539 Autism, x-linked, susceptibility to, 2 (finding) HPO C0848203 Male pelvic pain C0022116 Ischemia HSDN C4084775 Usual severity weight loss C0009759 Conjunctival diseases HSDN C0023380 Lethargy C0268560 Hyperglycinemia, transient neonatal HPO C0003862 Pain joint C0035243 Respiratory tract infections HSDN C0162292 Extraocular palsy C1848586 Intestinal pseudoobstruction with external ophthalmoplegia OrphaNet|MalaCards C0424755 Fever symptoms C0042870 Vitamin d deficiency HSDN C3887784 Decreased urine output C0039971 Thirst HSDN C0270948 Neurogenic muscular atrophy C0410173 Severe autosomal recessive muscular dystrophy of childhood - north african type (disorder) MalaCards|HPO C1963091 Diarrhea adverse event C0023976 Long qt syndrome HSDN C0013405 Dyspnea, paroxysmal C0018794 Heart block HSDN C0424755 Fever symptoms C0037929 Spinal cord injuries HSDN C0019079 Bloody sputum C0034067 Pulmonary emphysema HSDN C2984057 Have nausea C0003869 Arthritis, infectious HSDN C0018784 Deafness sensorineural C1853710 Hereditary motor and sensory neuropathy, type iic (disorder) MalaCards|HPO C0424755 Fever symptoms C1861753 Multiminicore disease, moderate, with hand involvement HPO C0013911 Emaciate C0040021 Thromboangiitis obliterans HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1510502 Oxyphilic adenoma HSDN C0027497 Queasy C0205788 Histiocytoid hemangioma HSDN C3274924 Have been coughing C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0013404 Respiratory difficulty C0006147 Breast fed HSDN C4084802 Usual severity diarrhea C0005283 Beta thalassemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1720830 Painful bladder syndrome OrphaNet|MalaCards C0085128 Cardiac output elevated C0020500 Hyperoxaluria HSDN C0035455 Rhinitis C3809706 Ciliary dyskinesia, primary, 28 MalaCards C0413252 Hypothermia due to exposure C0026896 Myasthenia gravis HSDN C2984058 Have pain C0006271 Bronchiolitis HSDN C0036572 Convulsion C1848917 Tay-sachs disease, pseudo-ab variant HPO C0036572 Convulsion C3552236 Polymicrogyria, symmetric or asymmetric UMLS C0004134 Dyssynergia C0751383 Juvenile neuronal ceroid lipofuscinosis OrphaNet|MalaCards C0042963 Symptoms vomiting C0013926 Aeroembolism HSDN C0030193 Sense of pain C0022570 Keratitis dentritic HSDN C0030552 Paralysis partial C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0221232 Welts C0029839 Other specified urticaria nos UMLS C0038002 Spleen enlargement C0023281 Leishmaniasis OrphaNet|MalaCards C0427055 Face weakness C0265239 Wildervanck's syndrome MalaCards C0018932 Bright red rectal bleeding C0043194 Wiskott-aldrich syndrome OrphaNet|HPO|MalaCards C0016199 Pain flank C0278677 Stage iii renal cell cancer UMLS C0011991 Loose stools C0041971 Tumor urethra HSDN C2029884 Hearing loss by exam C0020502 Hyperparathyroidism HSDN C4084768 Usual severity vomiting C0178282 Hernia of abdominal cavity HSDN C0042963 Symptoms vomiting C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0030193 Sense of pain C0027645 Neoplasm seeding HSDN C0018777 Deafness, conductive C0022665 Kidney neoplasm HSDN C3714552 Strength decreased C1333764 Gastric cronkhite canada polyposis MalaCards C0018681 Headache, cephalalgia C0040136 Thyroid neoplasm HSDN C4049644 Depression C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C1963091 Diarrhea adverse event C0085073 Prosthesis-related infection HSDN C0454644 Delayed language development C1970841 Mental retardation, x-linked 93 (disorder) HPO C0700292 Arterial hypoxaemia C1970344 Congenital disorder of glycosylation, type iif OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0015397 Disorder of eye HSDN C1557397 Adverse event associated with pain C0029443 Osteomyelitis HSDN C4084768 Usual severity vomiting C0011265 Presenile dementia HSDN C0085632 Listlessness C1848915 Gm2-gangliosidosis, adult chronic type HPO C1384666 Decreased hearing C0002940 Aneurysm HSDN C3539889 Pelvic pain increasing in severity C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084769 Vomiting frequency C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C2169806 Tic C0004361 Autogenic therapy HSDN C0917816 Deficiency mental C2931452 Hirschsprung disease, deafness and polydactyly MalaCards C0242936 Center pain C1879737 Aromatherapy and essential oils HSDN C3463815 Feel fatigue C0025289 Meningitis HSDN C1384666 Decreased hearing C1845095 Deafness, x-linked 5 (disorder) MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011127 Pressure ulcer HSDN C2700617 Irritation - emotion C1836327 Rhabdoid tumor predisposition syndrome 1 (disorder) MalaCards C0042963 Symptoms vomiting C0005937 Bone cysts HSDN C0242936 Center pain C0037228 Size perception HSDN C0424755 Fever symptoms C0162627 Skin diseases, bacterial HSDN C0042798 Vision dim C0878677 Glycogen storage disease type iib MalaCards|HPO C0003079 Pupillary inequality C0015409 Eye injuries penetrating HSDN C0700153 Myotonus C1321780 Hypomagnesmic tetany MalaCards C0000737 Abdomen pain C1333099 Colon oat cell carcinoma UMLS C2984057 Have nausea C0006147 Breast fed HSDN C2024893 Cardiovascular surgery result: fatigue C1963090 Dehydration adverse event HSDN C1963164 Lymphopenia adverse event C1859753 Acc with intestinal lymphangiectasia OrphaNet|MalaCards C0015672 Decreased energy C0206624 Hepatoblastoma MalaCards C0000737 Abdomen pain C0009021 Clonorchiasis DiseaseOntology C0000737 Abdomen pain C0018128 Graft occlusion, vascular HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014179 Endometritis HSDN C0454644 Delayed language development C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0030552 Paralysis partial C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0042963 Symptoms vomiting C0026785 Munchhausen syndrome HSDN C4084802 Usual severity diarrhea C0035258 Restless legs syndrome HSDN C2237041 Shox gene with short stature C0023003 Langer-giedion syndrome OrphaNet|HPO|MalaCards C3887873 Hearing loss C0027439 Nasopharyngeal neoplasms HSDN C4085317 Diarrhea frequency C0600564 Self-efficacy HSDN C4084784 Diarrhea C0276357 Swine influenza MalaCards C4084784 Diarrhea C0017150 Gastrinoma OrphaNet|MalaCards C0003862 Pain joint C1838280 Epiphyseal dysplasia, multiple, 1 OrphaNet|HPO|MalaCards C0040822 D tremors C0752125 Spinocerebellar ataxia type 7 MalaCards|HPO C0018772 Deafness C0265279 Kniest dysplasia OrphaNet|HPO|MalaCards C0018772 Deafness C3463824 Myelodysplastic syndrome HSDN C3274920 Have shortness of breath question C0155883 Chronic obstructive asthma MalaCards C0030193 Sense of pain C0701818 Choledocholithiasis HSDN C1963087 Constipation adverse event C0031069 Familial mediterranean fever OrphaNet|HPO C0003862 Pain joint C0038436 Post-traumatic stress disorder HSDN C0013404 Respiratory difficulty C0026590 Child mother relationship HSDN C0424853 Finger mass C0684456 Neoplasm of uncertain behavior of finger UMLS C0026838 Spasticity muscle C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C1549543 Administration method - pain C0242647 Mucosa-associated lymphoid tissue lymphoma HSDN C0042940 Disorder of voice C1839130 Dystonia 3, torsion, x-linked HSDN C2024893 Cardiovascular surgery result: fatigue C0220847 C hepatitis virus HSDN C0518090 Frequency of pain question C0010678 Cysticercosis HSDN C1963180 Neck pain adverse event C1706377 Memory device component HSDN C2830461 Other lack of expected normal physiological development in childhood C0497409 Other nutritional; endocrine; and metabolic disorders UMLS C0042928 Paralysis vocal cord C1860403 Congenital bilateral recurrent nerve paralysis and ptosis MalaCards C0857305 Thrombocytopenia purpura C0035243 Respiratory tract infections HSDN C0018772 Deafness C0752308 Hypoxia-ischemia, brain HSDN C0029163 Hemorrhage mouth C0206657 Alveolar soft part sarcoma HSDN C1319541 On examination - right eye proliferative diabetic retinopathy C0011164 Abnormal degeneration UMLS C0030232 Color loss C0007570 Celiac disease HSDN C0027497 Queasy C0019196 Hepatitis c DiseaseOntology|HSDN|MalaCards C3641756 Have diarrhea C0020459 Hyperinsulinism HSDN C0020538 Hbp C2931254 Alport syndrome, recessive type MalaCards C1961131 Cough adverse event C0003507 Aortic valve stenosis HSDN C0518090 Frequency of pain question C0036220 Kaposi sarcoma HSDN C0013421 Dystonia C0268465 Phenylketonuria ii MalaCards|HPO C4084802 Usual severity diarrhea C0038271 Stereotyped behavior HSDN C0557874 Global developmental delay C0026755 Multiple carboxylase deficiency OrphaNet|MalaCards C1963184 Nystagmus adverse event C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C1860844 Sparse, thin hair C0346104 Follicular atrophoderma and basal cell epitheliomata OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0040425 Tonsillitis HSDN C2237041 Shox gene with short stature C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C0727671 Red cross toothache drops C1548578 Location characteristic id - smoking HSDN C0162298 Stiffness joints C2350233 Antley-bixler syndrome phenotype MalaCards C3641756 Have diarrhea C0344435 Ventricular fibrillation by ecg finding HSDN C4085222 Nausea C0000771 Abnormalities, drug induced HSDN C0016199 Pain flank C1334978 Non-hereditary clear cell renal cell carcinoma UMLS C0007398 Catatonic C0270730 Mptp induced parkinsonism HSDN C0030486 Extremity paralysis, lower C0038981 Swayback HSDN C3815497 Cough C0024141 Lupus erythematosus, systemic HSDN C2984058 Have pain C0035439 Rheumatic heart disease HSDN C4049602 Hyperactivity C0751157 Fraxe syndrome MalaCards C0018772 Deafness C0009651 Conditioning operant HSDN C2911647 Weight gain adverse event C0015726 Focused anxiety HSDN C4084766 Vomiting C0005937 Bone cysts HSDN C2096293 Ent surgical result ear vertigo C0013990 Pathological accumulation of air in tissues HSDN C4084769 Vomiting frequency C0024266 Lymphocytic choriomeningitis DiseaseOntology|MalaCards C0030193 Sense of pain C0264003 Primary fibrositis UMLS C0012833 Dizzy C0456801 Ppv - peripheral positional vertigo UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0030922 Peptic ulcer hemorrhage HSDN C3697716 Acute flaccid paralysis C1405301 Poliomyelitis, paralytic MalaCards C4084725 Usual severity cough C0036421 Systemic scleroderma OrphaNet|HSDN|MalaCards C0042963 Symptoms vomiting C2987174 Vhl-associated pancreatic serous adenoma UMLS C0850758 Pain pelvic C0001442 Adenosarcoma HSDN C0004134 Dyssynergia C0268125 Purine-nucleoside phosphorylase deficiency HPO|UMLS C0013528 Echo speech C0751955 Brain infarction HSDN C4085661 Usual severity nausea C2004491 Cicatrix HSDN C0020673 Hypothermia (central) (local) C0015802 Femur fracture HSDN C0277873 Nasal flaring C4225416 Mental retardation, x-linked 99, syndromic, female-restricted UMLS C0235153 Sensory hallucination C0339852 Dermoids nasal MalaCards C0018784 Deafness sensorineural C0004943 Behcet syndrome HSDN C2984058 Have pain C0149654 Conduct disorder HSDN C0424755 Fever symptoms C0019294 Hernia, inguinal HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0019159 Hepatitis a HSDN C4084726 Distress cough C0152054 Therapeutic touch HSDN C0454644 Delayed language development C3806412 Mgcph MalaCards C0019079 Bloody sputum C0006267 Bronchiectasis UMLS C0040485 Wryneck C1414216 Dystonia 6, torsion (disorder) MalaCards|HPO|UMLS C3641756 Have diarrhea C0026936 Mycoplasma infections HSDN C0004604 Pain back C0004153 Atherosclerosis HSDN C1549543 Administration method - pain C0158328 Trigger finger HSDN C4084788 Have dizziness C0037937 Spine injury HSDN C0042798 Vision dim C0001418 Adenocarcinoma HSDN C4084784 Diarrhea C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0405084 Abnormal weight gain in pregnancy C0269672 Weight gain pregnancy excessive UMLS C4084767 Bothered by vomiting C0080179 Vertebra fracture HSDN C4084775 Usual severity weight loss C0243013 Base learn problems HSDN C4085661 Usual severity nausea C2936636 Anticipation, psychological HSDN C0039070 Collapse fleeting C0023418 Leukemia HSDN C0042798 Vision dim C1863198 Albinism, ocular, with sensorineural deafness (disorder) HPO C0700078 Deep tendon reflex decrease C1855255 Pseudoarylsulfatase a deficiency MalaCards|HPO C0035229 Respiratory function impaired C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0028432 Nose diseases HSDN C0009806 Constipate C0008149 Chlamydia infections HSDN C2911647 Weight gain adverse event C0034929 Reflex HSDN C4084775 Usual severity weight loss C0019202 Hepatolenticular degeneration OrphaNet|HSDN|HPO|MalaCards C0007398 Catatonic C0008088 Child psychiatry HSDN C0478662 Slowness+poor responsiveness C4067664 Attention deficit conduct and disruptive behavior disorders UMLS C2315100 Pediatric failure to thrive C1279481 X-linked combined immunodeficiency diseases MalaCards|HPO C0018777 Deafness, conductive C0013261 Duane retraction syndrome HSDN C0015468 Face pain C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084726 Distress cough C3202971 Non-infective endocarditis HSDN C2919142 Short stature adverse event C0086651 Mucopolysaccharidosis, mps-iv-a OrphaNet|MalaCards C0037315 Breathing disorder during sleeping C2930798 Alexanders leukodystrophy MalaCards C0020458 Hyperhydrosis C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0917816 Deficiency mental C3150986 Epileptic encephalopathy, early infantile, 7 MalaCards|HPO C1963087 Constipation adverse event C0011168 Deglutition disorders HSDN C0020578 Hyperventilate C1258104 Diffuse scleroderma HSDN C0019825 Voice hoarseness C1708649 Laryngeal adenosquamous carcinoma UMLS C4042891 Sleep wake disorders C0036346 Schizophrenia, childhood HSDN C4084726 Distress cough C1136033 Cutaneous mastocytosis MalaCards C4084802 Usual severity diarrhea C0241802 Arthritis, venereal MalaCards C0010520 Skin cyanosis C0015745 Ingestive behavior HSDN C4084788 Have dizziness C0022650 Kidney calculi HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1265748 Torsion HSDN C3887873 Hearing loss C1850552 Nephrosis deafness urinary tract digital malformation MalaCards C4085211 Pain distress question C0013117 Dreaming HSDN C0332573 Macula C0263340 Urticaria pigmentosa, infantile form UMLS C0018775 Hearing loss bilateral C0344315 Depressed mood HSDN C0020903 Illusion C0025202 Melanoma HSDN C3274924 Have been coughing C0042075 Urologic diseases HSDN C0015672 Decreased energy C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C2237041 Shox gene with short stature C0796062 Microcephaly-deafness syndrome OrphaNet|MalaCards C0004134 Dyssynergia C0270730 Mptp induced parkinsonism HSDN C0010200 Cough symptom C2240378 Cleft palate on exam HSDN C3539892 Pelvic pain in front C0001261 Actinomycosis HSDN C0020458 Hyperhydrosis C3151476 Mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MalaCards|HPO C0018989 Paresis of one side of body C0234138 Partial unilateral paresis UMLS C4085210 Usual severity pain C0021099 Impetigo HSDN C2919142 Short stature adverse event C0026707 Mucopolysaccharidosis iv OrphaNet|MalaCards C0007758 Cerebellar ataxia C0162309 Adrenoleukodystrophy MalaCards|HSDN C2936821 Spinal cerebrospinal fluid leak C0161408 Cranial nerve vii injuries HSDN C4084775 Usual severity weight loss C4050613 Anxiety scale (basc-2) HSDN C0020673 Hypothermia (central) (local) C0023434 Chronic lymphocytic leukemia HSDN C0004134 Dyssynergia C0026697 Mucolipidoses HSDN C0004134 Dyssynergia C0002016 Aleutian mink disease HSDN C0700078 Deep tendon reflex decrease C0751540 Morvan disease HPO C2237041 Shox gene with short stature C1843418 Niemann-pick disease, type f HPO C4084766 Vomiting C0010417 Cryptorchidism HSDN C0015732 Feces incontinence C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C1963090 Dehydration adverse event C1855115 Methylmalonic aciduria, mut(0) type HPO C0042798 Vision dim C0271097 Usher syndrome OrphaNet C2926613 Chest pain:finding:point in time:^patient:ordinal C0007099 Carcinoma in situ HSDN C3274924 Have been coughing C2586211 Thrombosis of blood vessel HSDN C0026826 High muscle tone C3280856 Ichthyosis, spastic quadriplegia, and mental retardation MalaCards C4084775 Usual severity weight loss C0410422 Chronic multifocal osteomyelitis OrphaNet|MalaCards C0030193 Sense of pain C0042162 Uveal neoplasms HSDN C1963137 Hydrocephalus adverse event C0018553 Hamartoma syndrome, multiple MalaCards C0018784 Deafness sensorineural C0021368 Inflammation HSDN C0851578 Disorder sleep C0349231 Phobic anxiety disorder HSDN C4085210 Usual severity pain C0025517 Metabolic diseases HSDN C0231528 Muscle pain generalized C0035460 Rhinitis, vasomotor HSDN C1963237 Insomnia adverse event C3178970 Entrapment, pudendal nerve MalaCards C0036396 Sciatica C0263866 Lumbago or sciatica due to displacement of intervertebral disc UMLS C1549543 Administration method - pain C0002382 Alveolar bone loss HSDN C0013404 Respiratory difficulty C0860603 Anxiety symptoms HSDN C1962972 Proteinuria adverse event C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084774 Have weight loss C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C1527344 Dysphonia C0221759 Brachial plexus neuritis HSDN C3887784 Decreased urine output C0023529 Leukomalacia, periventricular HSDN C0022107 Fussiness C0268689 Vitamin d-dependent rickets, type 1 HPO C0242936 Center pain C0008372 Intrahepatic cholestasis HSDN C0011991 Loose stools C3151147 Bile acid synthesis defect, congenital, 3 MalaCards|HPO|UMLS C0023014 Developmental disorder language C0002514 Amino acid metabolism, inborn errors HSDN C0011206 Delirium acute C0206255 Malaria vaccine HSDN C0009421 Comatose C0700327 Clinical findings relating to memory HSDN C2984058 Have pain C0035220 Respiratory distress syndrome, newborn HSDN C4084727 Cough frequency C0001969 Alcoholic intoxication HSDN C0020450 Hyperemesis gravidarum C0037036 Sialorrhea HSDN C0003962 Ascites C0019154 Hepatic vein thrombosis OrphaNet|HPO|MalaCards C0013405 Dyspnea, paroxysmal C0019285 Diaphragmatic hernia traumatic HSDN C0022346 Yellow skin C2937421 Prostatic hyperplasia HSDN C3714552 Strength decreased C1847839 Episodic ataxia, type 3 MalaCards|UMLS C0000737 Abdomen pain C0679360 Foodborne disease HSDN C0018991 Paralysis one side of body C0033975 Psychotic disorders HSDN C0038506 Stutter C0001175 Acquired immunodeficiency syndrome HSDN C0039070 Collapse fleeting C0031117 Peripheral neuropathy HSDN C0030193 Sense of pain C0001849 Aids dementia complex HSDN C0037317 Sleep disturbance C0220756 Niemann-pick disease, type c OrphaNet C0242936 Center pain C0162538 Immunoglobulin a deficiency (disorder) HSDN C4084776 Weight loss C0017160 Gastroenteritis HSDN C0019825 Voice hoarseness C0012979 Canine disease HSDN C1279888 Proteinuria of undiagnosed cause C0041328 Renal tuberculosis HSDN C0850758 Pain pelvic C0314657 Genetic predisposition HSDN C0013421 Dystonia C0393665 Multiple sclerosis, chronic progressive HSDN C0026858 Musculoskeletal pain C0023485 Precursor b-cell lymphoblastic leukemia-lymphoma HSDN C0151786 Weakness muscle C0039841 Thiamine deficiency HSDN C2242996 Tingling C0019625 Sinus histiocytosis MalaCards C0004604 Pain back C0006309 Brucellosis DiseaseOntology|MalaCards C4084774 Have weight loss C0022876 Premature obstetric labor HSDN C0018681 Headache, cephalalgia C0007932 Chagas' disease + no organ inv DiseaseOntology|MalaCards C0023530 Leukopenia C0032339 Rothmund-thomson syndrome MalaCards C0518090 Frequency of pain question C0010481 Cushing syndrome HSDN C1279888 Proteinuria of undiagnosed cause C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C2024893 Cardiovascular surgery result: fatigue C0038525 Subarachnoid hemorrhage HSDN C3898969 Have been vomiting C4015130 Inflammatory skin and bowel disease, neonatal, 2 MalaCards C0032617 High urine output C2931783 Amelogenesis imperfecta nephrocalcinosis MalaCards|UMLS C0013404 Respiratory difficulty C0034530 Injury radiation HSDN C0039870 Leanness C0525042 Feeding and eating disorders of childhood HSDN C4084784 Diarrhea C0342701 Transcobalamin ii deficiency MalaCards C0030193 Sense of pain C0085426 Gram-positive bacterial infections HSDN C1963091 Diarrhea adverse event C0001261 Actinomycosis HSDN C0018681 Headache, cephalalgia C0152276 Granulocytic sarcoma HSDN C0000737 Abdomen pain C0006057 Botulisms OrphaNet|MalaCards C0003079 Pupillary inequality C0206640 Ossifying fibroma HSDN C0011991 Loose stools C0036429 Sclerosis HSDN C0008031 Pain chest C0439840 Reflex motion descriptor HSDN C1549543 Administration method - pain C0042109 Urticaria HSDN C0851578 Disorder sleep C0022423 Judgement HSDN C0234523 Apraxia, classic C0027746 Nerve degeneration HSDN C0030486 Extremity paralysis, lower C0037315 Sleep apnea syndromes HSDN C0030552 Paralysis partial C0221043 Liddle syndrome OrphaNet|HSDN|HPO|MalaCards C0007758 Cerebellar ataxia C0022822 Hunchback formed after birth HSDN C0019572 Hairiness C3810265 Warburg micro syndrome 4 MalaCards C0030486 Extremity paralysis, lower C0007137 Squamous cell carcinoma HSDN C0008031 Pain chest C0036421 Systemic scleroderma OrphaNet|HSDN|MalaCards C3463815 Feel fatigue C0006840 Candidiasis HSDN C3539890 Pelvic pain causes awakening at night C0037313 Sleep HSDN C0002170 Alopecia disorders C0796092 Oculo-cerebro-cutaneous syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0162872 Aortic aneurysm, thoracic HSDN C4084768 Usual severity vomiting C0008149 Chlamydia infections HSDN C1963170 Hypothermia adverse event C0010823 Cytomegalovirus infections HSDN C1962972 Proteinuria adverse event C0011311 Dengue fever HSDN C0010200 Cough symptom C0027889 Hereditary sensory and autonomic neuropathies HSDN C1963180 Neck pain adverse event C2911643 Encounter due to family history of osteoporosis HSDN C0043094 Weight gain C2984330 Chagas disease pathway HSDN C4085317 Diarrhea frequency C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0038002 Spleen enlargement C3888317 Sialidosis, type 2 OrphaNet C0007398 Catatonic C0024141 Lupus erythematosus, systemic HSDN C4085210 Usual severity pain C0043124 West nile fever HSDN C0004134 Dyssynergia C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0242936 Center pain C1000587 Pemphigus HSDN C0023885 Liver abscess C0023903 Liver neoplasms MalaCards C2984058 Have pain C0016397 Focal infection HSDN C0028961 Urine output decreased C0024535 Malaria, falciparum HSDN C4020887 Photodysphoria C1864849 Retinal cone dystrophy 4 MalaCards C4085222 Nausea C0520679 Sleep apnea, obstructive HSDN C0018772 Deafness C1706377 Memory device component HSDN C0030232 Color loss C3463824 Myelodysplastic syndrome HSDN C4084802 Usual severity diarrhea C1535939 Pneumocystis jiroveci pneumonia HSDN C1557397 Adverse event associated with pain C0399352 Developmental absence of tooth HSDN C0011991 Loose stools C0003872 Arthritis, psoriatic HSDN C0018772 Deafness C0002875 Cooley's anemia HPO C0851578 Disorder sleep C0012546 Diphtheria HSDN C1549543 Administration method - pain C0206743 Rhabdoid tumor HSDN C0042024 Urine incontinence C0028768 Obsessive-compulsive disorder HSDN C0027497 Queasy C2717905 Hereditary angioedema types i and ii HSDN C0004134 Dyssynergia C1865981 Friedreich ataxia 2 MalaCards C3887638 Failure to thrive in infant C2931002 Congenital disorder of glycosylation type 1h MalaCards C1557397 Adverse event associated with pain C1456784 Paranoia HSDN C0018681 Headache, cephalalgia C1318533 Secondary polycythemia OrphaNet|MalaCards C4084776 Weight loss C0026650 Movement disorders HSDN C0009676 Confusion state C0034362 Q fever HSDN C0033377 Caudal displacement C3151302 Chromosome 13q14 deletion syndrome MalaCards C0518090 Frequency of pain question C0042063 Urogenital abnormalities HSDN C4084726 Distress cough C0013808 Electroconvulsive therapy HSDN C0013362 Dysarthrias C0282492 Sneddon syndrome MalaCards|HPO C4042891 Sleep wake disorders C1962986 Glaucoma adverse event HSDN C0424755 Fever symptoms C0030790 Pelvis infection HSDN C0002962 Angina C0030767 Grouping peer HSDN C0036572 Convulsion C0795822 8 rec syndrome OrphaNet|UMLS|MalaCards C0424755 Fever symptoms C0206062 Lung diseases, interstitial HSDN C4084784 Diarrhea C0033348 Language program HSDN C0018681 Headache, cephalalgia C0872996 Q fever vaccine HSDN C0000727 Abdomen acute C0017152 Gastritis HSDN C2984057 Have nausea C0018273 Growth disorders HSDN C3641756 Have diarrhea C0014859 Esophageal neoplasms HSDN C0040259 Tinea pedis C0001828 Agricultural workers' diseases HSDN C0011991 Loose stools C0275148 Poisoning of animal by plant HSDN C0010520 Skin cyanosis C0017658 Glomerulonephritis HSDN C3665347 Vision impaired C0265966 Hereditary benign intraepithelial dyskeratosis MalaCards C0008031 Pain chest C0748695 Sick sinus syndrome tachy brady type UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0520946 Emotional hypersensitivity HSDN C1963071 Back pain adverse event C0020701 Somatization disorder HSDN C0039070 Collapse fleeting C0007133 Carcinoma, papillary HSDN C0518090 Frequency of pain question C0041351 Tularemia HSDN C4084767 Bothered by vomiting C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C0030193 Sense of pain C0024449 Fungal mycetoma HSDN C4084784 Diarrhea C1553188 Hemolysis - observation HSDN C0015469 Facial paralysis C0026975 Myelitis HSDN C1963087 Constipation adverse event C0018099 Gout HSDN C0018524 Hallucinate C0424000 Feeling suicidal (finding) HSDN C1963087 Constipation adverse event C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C0018681 Headache, cephalalgia C0028796 Dermatitis, occupational HSDN C4084769 Vomiting frequency C0028768 Obsessive-compulsive disorder HSDN C0009460 Communication impairment C0026590 Child mother relationship HSDN C4084788 Have dizziness C0018939 Hematological disease HSDN C0557874 Global developmental delay C4015316 Epileptic encephalopathy, early infantile, 27 MalaCards C0151786 Weakness muscle C0004943 Behcet syndrome HSDN C0033774 Skin pruritus C0023473 Myeloid leukemia, chronic HSDN C3665386 Abnormal vision C0242387 Mandibulofacial dysostosis MalaCards|HPO C0221512 Ache stomach C0025229 Melioidosis DiseaseOntology|MalaCards C0015469 Facial paralysis C0410204 Myopathy, centronuclear, autosomal recessive HPO C0398650 Idiopathic thrombocytopenia purpura C1866119 Autoimmune lymphoproliferative syndrome, type ia MalaCards|HPO C0156317 Genital edema male C0017412 Genital diseases, male UMLS C4084776 Weight loss C0027643 Neoplasm recurrence, local HSDN C0007398 Catatonic C0004377 Automatism HSDN C0221170 Stiffness muscle C3495588 Acrocephalopolydactylous dysplasia MalaCards C1069915 Vertigo C0271829 Pendred's syndrome MalaCards|HPO C0497406 Over weight C0694533 Moderate obesity UMLS C0037317 Sleep disturbance C1834304 Amyotrophy, hereditary neuralgic MalaCards C1069915 Vertigo C0340485 Familial ventricular tachycardia MalaCards C0018784 Deafness sensorineural C0175703 Thrombocytopenia-absent radius syndrome MalaCards|HPO C3887638 Failure to thrive in infant C0013575 Ectodermal dysplasia MalaCards C0023014 Developmental disorder language C0038273 Stereotypic movement disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0038353 Stomach distended HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1328252 Mucocutaneous leishmaniasis HSDN C4084774 Have weight loss C0019061 Hemolytic-uremic syndrome HSDN C0270327 Bed wetting C3245525 Familial renal glucosuria MalaCards C0030193 Sense of pain C0026918 Mycobacterium infections HSDN C4084769 Vomiting frequency C0026640 Mouth neoplasms HSDN C0085602 Polydypsia C3544080 Congenital central diabetes insipidus OrphaNet C0031911 Pigment deposition C0024623 Malignant neoplasm of stomach MalaCards C1549543 Administration method - pain C0035228 Respiratory hypersensitivity HSDN C0003862 Pain joint C1564560 Cartilage fracture HSDN C0007758 Cerebellar ataxia C1854698 Multiple carboxylase deficiency, juvenile-onset OrphaNet|HPO|MalaCards C0012833 Dizzy C0033968 Psychotherapeutic technique HSDN C0242936 Center pain C0162700 Tick-borne diseases HSDN C0013395 Indigestion C0035854 Rosacea HSDN C0042571 Vertigo subjective C0001721 Emotional affect HSDN C0013404 Respiratory difficulty C0746206 Lung lul pulmonary infiltrate UMLS C0012833 Dizzy C0004610 Bacteremia HSDN C4049602 Hyperactivity C0016667 Fragile x syndrome MalaCards|HPO C0557874 Global developmental delay C1850055 Peho syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C0023470 Myeloid leukemia HSDN C0010200 Cough symptom C0264446 Cobaltosis UMLS C0028961 Urine output decreased C1566590 Delayed graft function HSDN C0521991 Stress symptom C2957420 Military operational stress reaction UMLS C0027497 Queasy C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C0018784 Deafness sensorineural C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards|HPO C0011991 Loose stools C0013100 Dracontiasis OrphaNet|MalaCards C0035229 Respiratory function impaired C0035934 Rubinstein-taybi syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0019372 Herpesviridae infections HSDN C0242936 Center pain C0043124 West nile fever HSDN C0005745 Blepharoptosis C1260409 Myasthenia gravis without acute exacerbation MalaCards C0424755 Fever symptoms C0043254 Injuries penetrating HSDN C1963087 Constipation adverse event C0036357 Psychology, schizophrenic HSDN C0917816 Deficiency mental C3806730 Mental retardation, x-linked 98 MalaCards C1519353 Skin eruption papular C0347403 Benign cephalic histiocytosis OrphaNet|MalaCards C0011168 Disorder deglutition C1836076 Amyotrophic lateral sclerosis, chmp2b-related MalaCards C1069915 Vertigo C0007137 Squamous cell carcinoma HSDN C0522224 Palsied C0020635 Hypopituitarism HSDN C0278152 Hemifacial spasms C0022336 Creutzfeldt-jakob disease HSDN C0026884 Muteness C0033975 Psychotic disorders HSDN C0086565 Liver function abnormal C0153459 Malignant neoplasm of body of pancreas MalaCards C1549543 Administration method - pain C0007117 Basal cell carcinoma HSDN C0018681 Headache, cephalalgia C0030521 Parathyroid neoplasms MalaCards|HSDN C0025287 Meningitis-like C0032285 Pneumonia HSDN C4084788 Have dizziness C0008066 Child behavior disorders HSDN C2237041 Shox gene with short stature C1846044 Adrenomyodystrophy OrphaNet|MalaCards C2911645 Weight loss adverse event C0029896 Disease, ent HSDN C0010520 Skin cyanosis C0205788 Histiocytoid hemangioma HSDN C0520966 Coordination impaired C1836395 Spinocerebellar ataxia 26 HPO|UMLS C3274924 Have been coughing C0276119 Q-fever pneumonia MalaCards C0424755 Fever symptoms C3661525 Autosomal recessive chronic granulomatous disease MalaCards C0085128 Cardiac output elevated C0002895 Anemia, sickle cell HSDN C0456800 Secondary endolymphatic hydrops C0206586 Endolymphatic hydrops UMLS C0034933 Abnormal reflexes C0003892 Neurogenic arthropathy HSDN C0162292 Extraocular palsy C1839320 Childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness MalaCards C0018991 Paralysis one side of body C0020443 Hypercholesterolemia HSDN C0018772 Deafness C4084909 Depression subordinate domain HSDN C0040822 D tremors C0878578 Orthostatic tremor primary OrphaNet|MalaCards C0042940 Disorder of voice C0012979 Canine disease HSDN C0150055 Pain chronic C0007286 Carpal tunnel syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023267 Fibroid tumor HSDN C1557397 Adverse event associated with pain C0023892 Biliary cirrhosis HSDN C0036396 Sciatica C0018188 Granuloma HSDN C4020887 Photodysphoria C0544855 Leukonychia totalis OrphaNet|HPO|MalaCards C0030794 Pelvis pain C0026857 Musculoskeletal diseases HSDN C0033377 Caudal displacement C0796033 Marden-walker syndrome MalaCards|HPO C1549543 Administration method - pain C0036093 Salivary gland diseases HSDN C0042963 Symptoms vomiting C0004161 Athletic injuries HSDN C1963086 Confusion adverse event C0015632 Encephalitis, far eastern russian MalaCards C0010200 Cough symptom C2117118 X-ray of toe: deformity contracture HSDN C0019214 Hepatosplenomegaly C1856301 Gsd iv, classic hepatic HPO C0015469 Facial paralysis C0026857 Musculoskeletal diseases HSDN C0013604 Edematous C0023896 Alcoholic liver diseases HSDN C0000737 Abdomen pain C0600041 Infective cystitis HSDN C4084723 Constipation C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C2931183 Faces syndrome OrphaNet|MalaCards C0751837 Gait ataxic C0268514 Urocanase deficiency OrphaNet|HPO|MalaCards C4085211 Pain distress question C0030299 Pancreatic pseudocyst HSDN C2024893 Cardiovascular surgery result: fatigue C0019069 Hemophilia a HSDN C0237326 Defecation pain C1335686 Neuroendocrine neoplasm of rectum MalaCards C0015230 Exanthem C0406313 Psoriasis diffusa UMLS C0011991 Loose stools C0031212 Personality disorders HSDN C4085317 Diarrhea frequency C0032344 Poisoning aspects HSDN C0344315 Mood depressed C1862939 Amyotrophic lateral sclerosis 1 MalaCards C4084768 Usual severity vomiting C0037933 Spinal diseases HSDN C0033774 Skin pruritus C0549201 Asteatosis UMLS C0848203 Male pelvic pain C0033578 Prostatic neoplasms HSDN C0242936 Center pain C0085315 Toxoplasmosis, cerebral HSDN C0423714 Genitofemoral nerve neuralgia C1290878 Disease of thigh UMLS C0340288 Angina stable C0242698 Ventricular dysfunction, left HSDN C0271215 Blindness legal C0339527 Leber congenital amaurosis HPO C0042963 Symptoms vomiting C3149848 Variegate porphyria, homozygous variant HPO C1510417 Apraxia of gait C0221002 Hyperparathyroidism, primary HSDN C4085317 Diarrhea frequency C3151147 Bile acid synthesis defect, congenital, 3 MalaCards|HPO C4084724 Usual severity constipation C0029408 Degenerative polyarthritis HSDN C0042963 Symptoms vomiting C0023895 Liver diseases HSDN C4085862 Bothered by nausea C0242342 Sheehan syndrome OrphaNet|MalaCards C4084766 Vomiting C0026953 Mycotoxicoses HSDN C0043094 Weight gain C0026266 Mitral valve insufficiency HSDN C1549543 Administration method - pain C0015558 Fallopian tube neoplasms HSDN C1962972 Proteinuria adverse event C0023895 Liver diseases HSDN C0150055 Pain chronic C0004275 Attitude health HSDN C0557874 Global developmental delay C2931737 Hersh podruch weisskopk syndrome MalaCards C0497406 Over weight C0520676 Premenstrual dysphoric disorder HSDN C2919142 Short stature adverse event C1968740 Glycogen storage disease iiib HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0038187 Starvation HSDN C0015468 Face pain C3495559 Juvenile arthritis HSDN C0000737 Abdomen pain C1335690 Rectal squamous carcinoma UMLS C0030193 Sense of pain C0085278 Antiphospholipid syndrome HSDN C0239667 Forearm pain C0741096 Upper_ext problem UMLS C4084768 Usual severity vomiting C0003469 Anxiety disorders HSDN C0009460 Communication impairment C0008090 Child reactive disorder HSDN C4084725 Usual severity cough C0004576 Babesiosis OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0013238 Dry eye syndromes HSDN C3463815 Feel fatigue C0032965 Pregnancy complications, infectious HSDN C0221166 Paraparesis C0018946 Hematoma, subdural HSDN C0019825 Voice hoarseness C1532560 Plasmacytoma - category HSDN C0000731 Abdomen distention C0334489 Pancreatoblastoma MalaCards C0023530 Leukopenia C2675511 Diamond-blackfan anemia 8 MalaCards C4084784 Diarrhea C0034530 Injury radiation HSDN C4084775 Usual severity weight loss C0040456 Tooth impaction HSDN C0026838 Spasticity muscle C0042830 Perception visual HSDN C0007758 Cerebellar ataxia C0009240 Cognition HSDN C0036572 Convulsion C1838491 Kuzniecky syndrome OrphaNet|UMLS|MalaCards C0015672 Decreased energy C0016510 Foot diseases HSDN C0004134 Dyssynergia C0003507 Aortic valve stenosis HSDN C0036572 Convulsion C0041834 Erythema HSDN C0026826 High muscle tone C3281029 Rigidity and multifocal seizure syndrome, lethal neonatal MalaCards C0004134 Dyssynergia C0026848 Myopathy HSDN C2984057 Have nausea C1837218 Cleft palate, isolated HSDN C0333243 Edema pitting C1719313 Hereditary amyloid nephropathy MalaCards C4085210 Usual severity pain C0236664 Alcohol-related disorders HSDN C4084774 Have weight loss C0009062 Clostridia infection HSDN C0152227 Tearing excessive C1846529 Cone-rod dystrophy 10 MalaCards|HPO C1549543 Administration method - pain C0036285 Scarlet fever HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0013405 Dyspnea, paroxysmal C0006267 Bronchiectasis HSDN C2237041 Shox gene with short stature C0265342 Cerebrocostomandibular syndrome OrphaNet|HPO|MalaCards C1279888 Proteinuria of undiagnosed cause C0043065 Water electrolyte imbalance HSDN C0557874 Global developmental delay C3810278 Joubert syndrome 22 MalaCards C0009398 Color vision defects C3552852 Retinitis pigmentosa 65 MalaCards C1384666 Decreased hearing C0376634 Craniofacial abnormalities HSDN C0018991 Paralysis one side of body C0270788 Paralytic syndrome UMLS C0012569 Double vision C0030472 Paraneoplastic syndromes HSDN C0030554 Abnormal sensation C1258666 Myxoid cyst HSDN C0008031 Pain chest C0206141 Idiopathic hypereosinophilic syndrome HSDN C0043094 Weight gain C0221752 Rbc urine HSDN C1962972 Proteinuria adverse event C0030286 Pancreatic diseases HSDN C1963170 Hypothermia adverse event C0028768 Obsessive-compulsive disorder HSDN C0013604 Edematous C0019829 Hodgkin disease HSDN C0151825 Ostalgia C0342646 Vitamin d-dependent rickets, type 2a HPO|UMLS C0851578 Disorder sleep C1290398 Cerebral arterial aneurysm HSDN C2024878 Cardiovascular surgery result: dyspnea C0007133 Carcinoma, papillary HSDN C4085661 Usual severity nausea C0023895 Liver diseases HSDN C0026838 Spasticity muscle C0016510 Foot diseases HSDN C3829611 Nausea frequency C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C0577572 Mass of musculoskeletal structure C0276013 Gumma, bone of yaws UMLS C4084774 Have weight loss C0302363 Bang disease MalaCards C4085211 Pain distress question C0338473 Neuroaxonal dystrophies HSDN C0086437 Joint hypermobility C3149814 Retinal dystrophy, early-onset, with pituitary dysfunction HPO C2203646 Jaundice C0033817 Pseudomonas infections HSDN C4084784 Diarrhea C0030283 Pancreatic cyst HSDN C0040264 Ear ringing sound C1710146 Familial spinal arachnoiditis MalaCards C0700078 Deep tendon reflex decrease C3808991 Congenital disorder of deglycosylation MalaCards C0151596 Discoloration tongue C0235347 Black furry tongue UMLS C2911645 Weight loss adverse event C0032227 Pleural effusion disorder HSDN C4084727 Cough frequency C1546847 Entity name part type - family HSDN C2911645 Weight loss adverse event C0038941 Incisional infection HSDN C2911647 Weight gain adverse event C0600519 Ventricular remodeling HSDN C0242936 Center pain C0015618 Families therapy HSDN C4085317 Diarrhea frequency C0014342 Bluecomb of turkeys HSDN C0234146 Absent reflex C0265316 Neurocutaneous syndromes MalaCards C0917967 Pupil function anomaly C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0242936 Center pain C0014856 Esophageal fistula HSDN C0040822 D tremors C0034345 Pyruvate dehydrogenase complex deficiency disease OrphaNet|MalaCards C0030552 Paralysis partial C4085311 Depression - recess HSDN C3641756 Have diarrhea C0035220 Respiratory distress syndrome, newborn HSDN C3887638 Failure to thrive in infant C1846142 Hoyeraal-hreidarsson syndrome OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0206062 Lung diseases, interstitial HSDN C0018784 Deafness sensorineural C1838180 Codas syndrome OrphaNet|HPO|MalaCards C0727671 Red cross toothache drops C0013240 Alveolar osteitis HSDN C4084784 Diarrhea C0032045 Placenta disorders HSDN C0917801 Sleep disorder insomnia C3178970 Entrapment, pudendal nerve MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0019196 Hepatitis c HSDN C4085661 Usual severity nausea C0004352 Autistic disorder HSDN C0042571 Vertigo subjective C0034186 Pyelonephritis HSDN C3829611 Nausea frequency C0011884 Diabetic retinopathy HSDN C0030552 Paralysis partial C0027145 Myxedema MalaCards C0750394 Wbc low C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C1963087 Constipation adverse event C3241945 Melena due to gastrointestinal hemorrhage HSDN C0232466 Feeding difficulty C0002875 Cooley's anemia OrphaNet|HPO C0007758 Cerebellar ataxia C0006105 Brain abscess HSDN C4084784 Diarrhea C3668816 Inflammation of non-human mammary gland HSDN C1963154 Renal failure adverse event C1859568 Bardet-biedl syndrome 10 MalaCards C0344315 Mood depressed C1864851 Pigmented nodular adrenocortical disease, primary, 2 HPO C0018991 Paralysis one side of body C0027149 Myxoma HSDN C4084802 Usual severity diarrhea C0040127 Thyroid crisis HSDN C0234132 Pyramidal sign C4020654 Obsolete corticospinal tract disease in lower limbs UMLS C0026821 Cramp C0039082 Syndrome HSDN C0851578 Disorder sleep C0026640 Mouth neoplasms HSDN C0727671 Red cross toothache drops C1956346 Coronary artery disease HSDN C0015469 Facial paralysis C0027059 Myocarditis HSDN C2919142 Short stature adverse event C0037231 Sjogren-larsson syndrome MalaCards|HPO C0042928 Paralysis vocal cord C0024299 Lymphoma HSDN C1069915 Vertigo C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C2984058 Have pain C0040799 Traumatic subcutaneous emphysema HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018915 Hemangioendothelioma HSDN C0042024 Urine incontinence C0018273 Growth disorders HSDN C4085222 Nausea C3711850 Opticospinal multiple sclerosis MalaCards C1962972 Proteinuria adverse event C0542241 Toxemia bacterial HSDN C4085222 Nausea C0002395 Alzheimer's disease HSDN C0424755 Fever symptoms C0003469 Anxiety disorders HSDN C0150055 Pain chronic C0001430 Adenoma HSDN C3641756 Have diarrhea C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C3641755 Have constipation C0007820 Cerebrovascular disorders HSDN C0033774 Skin pruritus C0040252 Tinea corporis (disorder) MalaCards C0033774 Skin pruritus C0006147 Breast fed HSDN C0018777 Deafness, conductive C1510455 Acrocephalosyndactylia OrphaNet|HPO|MalaCards C0012833 Dizzy C0014055 Encephalitis, epidemic HSDN C1963087 Constipation adverse event C0040336 Tobacco use disorder HSDN C0007859 Pain neck C0037650 Somatoform disorder HSDN C0010200 Cough symptom C0025284 Meningeal neoplasms HSDN C1963071 Back pain adverse event C0001815 Primary myelofibrosis HSDN C0011175 Deficient fluid volume C1846343 Bartter syndrome, type 3 MalaCards|HPO C4085661 Usual severity nausea C0016510 Foot diseases HSDN C2029884 Hearing loss by exam C0043167 Pertussis HSDN C0019209 Large liver C2239176 Liver carcinoma MalaCards C0042963 Symptoms vomiting C3278664 Liver failure, infantile, transient UMLS C0005745 Blepharoptosis C3550903 Cornelia de lange syndrome 5 MalaCards C0008031 Pain chest C1306759 Eosinophilic disorder HSDN C4084773 Bothered by weight gain C0006736 Body stone HSDN C3463815 Feel fatigue C0018133 Graft-vs-host disease HSDN C0030200 Intractable pain C0019693 Hiv infections HSDN C0035078 Failure kidney C0265246 Townes syndrome OrphaNet|HPO|MalaCards C0848203 Male pelvic pain C1962979 Burn adverse event HSDN C4084784 Diarrhea C1504665 Products used to treat diabetic ketoacidosis HSDN C1291078 Epigastric discomfort C0859015 Irritability; stomach UMLS C3463815 Feel fatigue C0342637 Hypocalciuric hypercalcemia, familial, type 1 MalaCards C0003467 Angst C3683846 Chromosome 17p deletion syndrome MalaCards C3898969 Have been vomiting C0025500 Mesothelioma HSDN C4084802 Usual severity diarrhea C3495559 Juvenile arthritis HSDN C0270948 Neurogenic muscular atrophy C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C0020673 Hypothermia (central) (local) C0016658 Fracture bone HSDN C2237041 Shox gene with short stature C0265343 Jarcho-levin syndrome OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C4084909 Depression subordinate domain HSDN C4084725 Usual severity cough C0008073 Developmental disabilities HSDN C0013362 Dysarthrias C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C0600142 Flash hot C1963064 Anxiety adverse event HSDN C3829611 Nausea frequency C0235146 Emotionally high HSDN C4084775 Usual severity weight loss C0037939 Spinal neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043124 West nile fever HSDN C0043094 Weight gain C0032227 Pleural effusion disorder HSDN C0497406 Over weight C0023890 Liver cirrhosis HSDN C2911645 Weight loss adverse event C0032019 Pituitary neoplasms HSDN C0003862 Pain joint C0020538 Hypertensive disease HSDN C0024031 Back pain lower back C0270611 Brain damage HSDN C0042963 Symptoms vomiting C0042134 Uterine hemorrhage HSDN C0426579 Anorexia symptom C0341480 Pancreas, cyst, congenital MalaCards C0030554 Abnormal sensation C3814530 Skin vesicle HSDN C0349588 Stature short C0398791 Nijmegen breakage syndrome OrphaNet|HPO|MalaCards C0007166 Cardiac output decreased C0007786 Brain ischemia HSDN C2911647 Weight gain adverse event C0149931 Migraine disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038874 Supratentorial neoplasms HSDN C4085862 Bothered by nausea C4041080 Neurocognitive disorders HSDN C2919142 Short stature adverse event C1850168 Bruck syndrome 1 OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C1999266 Depression adverse event HSDN C2984058 Have pain C0019195 Hepatitis, viral, human HSDN C1963170 Hypothermia adverse event C0003507 Aortic valve stenosis HSDN C2024878 Cardiovascular surgery result: dyspnea C2004491 Cicatrix HSDN C0234132 Pyramidal sign C0342803 Dihydropyrimidinase deficiency HPO C0162298 Stiffness joints C1444838 Chronic arthritis of juvenile onset OrphaNet C0157725 Other spec pruritic conditions C0406044 Other pruritic conditions nos UMLS C0011991 Loose stools C0014848 Esophageal achalasia HSDN C0036572 Convulsion C0009952 Febrile convulsions UMLS C1963086 Confusion adverse event C0003811 Cardiac arrhythmia HSDN C0393588 Dystonias paroxysmal C0393587 Kinesiogenic choreoathetosis UMLS C3641755 Have constipation C3493776 Hypothyroidism, congenital, nongoitrous, 1 MalaCards C0234512 Prosopagnosia C0009240 Cognition HSDN C0009806 Constipate C0042373 Vascular diseases HSDN C0028961 Urine output decreased C2930957 Hantavirosis OrphaNet|MalaCards C0020505 Excessive eating C0017979 Glycosuria HSDN C0039070 Collapse fleeting C1843738 Long qt syndrome 1, acquired, susceptibility to HPO C3146279 Coma C0009492 Compartment syndromes HSDN C0011168 Disorder deglutition C0396059 Familial vocal cord dysfunction MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0162316 Iron deficiency anemia HSDN C0004134 Dyssynergia C0029134 Optic neuritis HSDN C1963154 Renal failure adverse event C1304205 Neutrophilic urticaria MalaCards C0030552 Paralysis partial C0016542 Foreign body HSDN C0042024 Urine incontinence C1136220 Counseling, directive HSDN C0557874 Global developmental delay C2674937 Chromosome 10q26 deletion syndrome MalaCards C1963071 Back pain adverse event C0153458 Pancreas head cancer malignant MalaCards C0022638 Ketosis C0016756 Fructose-1,6-diphosphatase deficiency MalaCards|HPO C0005745 Blepharoptosis C0265205 Robinow syndrome MalaCards C0040264 Ear ringing sound C0030421 Paraganglioma HSDN C0518090 Frequency of pain question C1527311 Brain edema HSDN C2165501 Depressed fetal heart sounds C2165502 Depressed fetal heart sounds antepartum condition or complication UMLS C0413252 Hypothermia due to exposure C1963083 Cholecystitis adverse event HSDN C0019572 Hairiness C2931277 Pena shokeir syndrome type 2 MalaCards C2242996 Tingling C0031350 Pharyngitis HSDN C3463815 Feel fatigue C0233610 Negativism in catatonia HSDN C0454597 Dysarthria flaccid C0013362 Dysarthria UMLS C0030554 Abnormal sensation C0017181 Gastrointestinal hemorrhage HSDN C0005745 Blepharoptosis C0085077 Sweet syndrome MalaCards C0037763 Spasm C2678194 Mental retardation, x-linked, syndromic, christianson type HPO C0015230 Exanthem C0857100 Extensive rash of legs UMLS C4085210 Usual severity pain C0011848 Diabetes insipidus HSDN C0027498 Nausea vomiting C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0206682 Follicular thyroid carcinoma HSDN C0015938 Fetal macrosomia C0032964 Pregnancy complications, hematologic HSDN C0040822 D tremors C0026946 Mycoses HSDN C0013604 Edematous C0033860 Psoriasis HSDN C0151825 Ostalgia C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C1961131 Cough adverse event C0032966 Complication, neoplastic pregnancy HSDN C0023015 Language handicap C1963064 Anxiety adverse event HSDN C0037316 Not enough sleeping C1145670 Respiratory failure HSDN C3274924 Have been coughing C0019284 Diaphragmatic hernia HSDN C0042798 Vision dim C2746069 Familial ectopia lentis MalaCards|HPO C4084802 Usual severity diarrhea C3281289 Trichohepatoenteric syndrome 2 MalaCards C0424755 Fever symptoms C3887654 Polyarteritis nodosa, childhood-onset MalaCards C3541349 Syncope C1881674 Medical device emits smoke HSDN C0700590 Diaphoresis excessive C0001206 Acromegaly OrphaNet|HPO|MalaCards C0015230 Exanthem C2931518 Plexosarcoma MalaCards C0349506 Sun sensitivity C0018203 Chronic granulomatous disease OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0007134 Renal cell carcinoma HSDN C0424755 Fever symptoms C1527429 Increased blood npn HSDN C0039870 Leanness C0001973 Alcoholic intoxication, chronic HSDN C2010840 Generalized soft tissue swelling C0037580 Soft tissue swelling UMLS C4085211 Pain distress question C0019061 Hemolytic-uremic syndrome HSDN C0042024 Urine incontinence C0037579 Soft tissue neoplasms HSDN C0151686 Growth retardation C2678492 Sex reversal, female, with dysgenesis of kidneys, adrenals, and lungs HPO C4084775 Usual severity weight loss C1868649 Panic disorder 1 HSDN C0151818 Opisthotonos C0003803 Arnold chiari malformation MalaCards C0020450 Hyperemesis gravidarum C0796561 Melanoma vaccines HSDN C0242936 Center pain C0019310 Hernia, obturator HSDN C4084774 Have weight loss C0028960 Oligospermia HSDN C0003811 Cardiac rhythm disturbance C1840334 Hypoparathyroidism, autosomal recessive MalaCards C4084775 Usual severity weight loss C1253937 Pericardial effusion HSDN C4084725 Usual severity cough C1540912 Hypereosinophilic syndrome HSDN C2315100 Pediatric failure to thrive C1865270 Bartter syndrome, type 4a HPO C0030193 Sense of pain C0031069 Familial mediterranean fever HSDN C1962972 Proteinuria adverse event C1854336 Paragangliomas 3 MalaCards C1836296 Lower extremity weakness C1833373 Inclusion body myopathy, autosomal recessive OrphaNet|MalaCards C0152200 Achromatism C0302129 Achromatopsia 1 MalaCards C0271215 Blindness legal C1846331 Juvenile-onset dystonia MalaCards C0015230 Exanthem C1274262 Miliaria rubra, infantile UMLS C4084776 Weight loss C0022876 Premature obstetric labor HSDN C4085210 Usual severity pain C0001249 Actinobacillus infections HSDN C4085210 Usual severity pain C0023443 Hairy cell leukemia HSDN C0038002 Spleen enlargement C0026764 Multiple myeloma HPO C1963252 Tremor adverse event C0027819 Neuroblastoma HSDN C4085222 Nausea C0270858 Abdominal migraines MalaCards C4084723 Constipation C0023892 Biliary cirrhosis HSDN C0026884 Muteness C2937358 Cerebral hemorrhage HSDN C2024878 Cardiovascular surgery result: dyspnea C0439840 Reflex motion descriptor HSDN C4085549 Dizziness C0010964 Dandy-walker syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0314657 Genetic predisposition HSDN C0018784 Deafness sensorineural C0003509 Aortitis, nos HSDN C4085211 Pain distress question C0035229 Respiratory insufficiency HSDN C3641756 Have diarrhea C0018051 Gonadal dysgenesis HSDN C1549543 Administration method - pain C0238417 Scorpion sting HSDN C0454644 Delayed language development C1861129 Takao vcf syndrome HPO C4085862 Bothered by nausea C1720777 Functional laterality HSDN C4085210 Usual severity pain C0242231 Coronary stenosis HSDN C0917816 Deficiency mental C0796085 Nance-horan syndrome OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0004114 Astrocytoma HSDN C4084774 Have weight loss C0151740 Intracranial hypertension HSDN C4084726 Distress cough C0014541 Epiglottitis HSDN C4084726 Distress cough C3161104 Adult plch MalaCards C0497247 Blood pressure elevation C0020428 Hyperaldosteronism MalaCards C0242936 Center pain C0521170 Fracture due to osteoporosis HSDN C0233514 Behavior abnormal C0795907 Conotruncal anomaly face syndrome MalaCards C0751295 Memory loss or impairment C1843013 Alzheimer disease, familial, type 3 HPO|UMLS C2984058 Have pain C0026590 Child mother relationship HSDN C0007758 Cerebellar ataxia C0018523 Hallervorden-spatz syndrome MalaCards|HPO C1384666 Decreased hearing C1412747 Bbs2 gene HPO C0221166 Paraparesis C0270788 Paralytic syndrome UMLS C1090821 Sepsis C0042781 Visceral myopathy MalaCards C0018681 Headache, cephalalgia C0018128 Graft occlusion, vascular HSDN C0033774 Skin pruritus C0040923 Vaginitis trichomonas HSDN C0013604 Edematous C0032963 Pregnancy complications, cardiovascular HSDN C4085211 Pain distress question C0079631 Interdisciplinary communication HSDN C0242936 Center pain C0026764 Multiple myeloma HSDN C1069915 Vertigo C0011989 Camurati-engelmann syndrome HSDN C1557397 Adverse event associated with pain C0405580 Adrenal cortical hypofunction HSDN C0036572 Convulsion C1291560 Deficiency of glutamate decarboxylase OrphaNet|MalaCards C4084802 Usual severity diarrhea C1134719 Invasive ductal breast carcinoma HSDN C0009421 Comatose C1701940 Pneumonia, ventilator-associated HSDN C0008031 Pain chest C0007134 Renal cell carcinoma HSDN C1549543 Administration method - pain C0036095 Salivary gland neoplasms HSDN C0004134 Dyssynergia C0001969 Alcoholic intoxication HSDN C0036572 Convulsion C0013504 Echinococcosis, hepatic HSDN C0587246 Extremity weakness C1853949 Myasthenia, familial infantile, 1 MalaCards|HPO C4084776 Weight loss C0018523 Hallervorden-spatz syndrome OrphaNet|MalaCards C0020672 Body temperature decreased C0302148 Blood clot HSDN C0151686 Growth retardation C2751630 Dursun syndrome HPO C0011991 Loose stools C0008073 Developmental disabilities HSDN C1963184 Nystagmus adverse event C0398691 Hyperimmunoglobulinemia d MalaCards C4084784 Diarrhea C0018824 Heart valve disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0037054 Sickle cell trait MalaCards|HSDN C1963249 Tinnitus adverse event C3150933 Hyperaldosteronism, familial, type iii MalaCards C0007758 Cerebellar ataxia C1842577 Joubert syndrome 2 MalaCards|HPO C0237326 Defecation pain C0271737 Addison's disease due to autoimmunity OrphaNet C1069915 Vertigo C1962979 Burn adverse event HSDN C3541349 Syncope C1853554 Radiation induced meningioma MalaCards C0454644 Delayed language development C2675179 Arginine:glycine amidinotransferase deficiency MalaCards|HPO C2029884 Hearing loss by exam C1963274 Vasculitis adverse event HSDN C3665347 Vision impaired C2751780 Retinitis pigmentosa, juvenile, spata7-related HPO C1856661 Cornea cloudy C0020725 Type ii mucolipidosis MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0009241 Cognition disorders HSDN C3898969 Have been vomiting C0152998 Acute nonparalytic poliomyelitis, poliovirus, unspecified type DiseaseOntology|MalaCards C0700292 Arterial hypoxaemia C0002895 Anemia, sickle cell MalaCards|HPO C0037317 Sleep disturbance C2931673 Ceroid lipofuscinosis, neuronal 1, infantile MalaCards|HPO C2984057 Have nausea C0302497 Retrobulbar haemorrhage HSDN C4084727 Cough frequency C0018133 Graft-vs-host disease HSDN C0040485 Wryneck C1579931 Depressed - symptom HSDN C4084775 Usual severity weight loss C0013182 Drug allergy HSDN C0518090 Frequency of pain question C0035229 Respiratory insufficiency HSDN C1549543 Administration method - pain C0041956 Ureteral obstruction HSDN C0042928 Paralysis vocal cord C1510412 Pseudoaneurysm HSDN C0426579 Anorexia symptom C0019829 Hodgkin disease OrphaNet C0349588 Stature short C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards|HPO C0577569 Mass of male genital structure C3696981 Paratesticular malignant neoplasm UMLS C0231835 Respiration rate increased C0152061 Louse-borne relapsing fever, nos DiseaseOntology|MalaCards C0037315 Breathing disorder during sleeping C0010276 Craniopharyngioma MalaCards|HPO C1384666 Decreased hearing C0242292 Mccune-albright syndrome HPO C2984057 Have nausea C0018790 Cardiac arrest HSDN C2984058 Have pain C0035457 Rhinitis, allergic, perennial HSDN C0008031 Pain chest C0018099 Gout HSDN C0030193 Sense of pain C0014547 Epilepsies, partial HSDN C0027796 Neuralgias C2937358 Cerebral hemorrhage HSDN C1279888 Proteinuria of undiagnosed cause C2984572 Malaria pathway HSDN C0013404 Respiratory difficulty C1709781 Pyothorax-associated lymphoma UMLS C3146279 Coma C0007361 Cat-scratch disease HSDN C0242936 Center pain C0035328 Retinal vein occlusion HSDN C0036572 Convulsion C0278199 Seizure, partial, with impaired consciousness UMLS C0043144 Wheeze C0878555 Diffuse panbronchiolitis MalaCards|UMLS C0015672 Decreased energy C1261473 Sarcoma HSDN C4042891 Sleep wake disorders C0425045 Sudden infant death HSDN C0018681 Headache, cephalalgia C0035126 Reperfusion injury HSDN C1962956 Flatulence adverse event C0008350 Cholelithiasis HSDN C2984058 Have pain C0037859 Spermatocele HSDN C0398650 Idiopathic thrombocytopenia purpura C0033860 Psoriasis HSDN C4085210 Usual severity pain C0006437 Burn, inhalation HSDN C0277873 Nasal flaring C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards|HPO|UMLS C2984057 Have nausea C2586211 Thrombosis of blood vessel HSDN C0020450 Hyperemesis gravidarum C0034530 Injury radiation HSDN C1962972 Proteinuria adverse event C2025995 Cellulitis HSDN C0023012 Delay language C1858054 Bardet-biedl syndrome 6 HPO C0017181 Gastrointestinal bleed C0004943 Behcet syndrome OrphaNet|HPO|MalaCards C4084725 Usual severity cough C0017416 Genital neoplasms, female HSDN C0042928 Paralysis vocal cord C0004610 Bacteremia HSDN C2984058 Have pain C0010606 Adenoid cystic carcinoma HSDN C1565249 Limitation, mobility C0009917 Contracture HSDN C4085210 Usual severity pain C0038363 Aphthous stomatitis HSDN C0021359 Infertility C2931783 Amelogenesis imperfecta nephrocalcinosis MalaCards C0008031 Pain chest C0013743 Eisenmenger complex HSDN C0036572 Convulsion C0015938 Fetal macrosomia MalaCards C1549543 Administration method - pain C3542413 Cdisc adas-cog - comprehension HSDN C0497366 Change skin color C0041834 Erythema UMLS C0030193 Sense of pain C1707300 Cardiac intramuscular hemangioma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0040100 Thymoma HSDN C0012833 Dizzy C0027051 Myocardial infarction HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0004239 Atrial flutter HSDN C0042963 Symptoms vomiting C0022890 Labyrinthine disorder HSDN C1963091 Diarrhea adverse event C0019326 Ventral hernia HSDN C4085317 Diarrhea frequency C1963709 Abetalipoproteinemia (lab finding) HSDN C0009806 Constipate C1550639 Specimen type - fistula HSDN C0009421 Comatose C0040136 Thyroid neoplasm HSDN C0035229 Respiratory function impaired C1841854 Gms syndrome OrphaNet|MalaCards C1963077 Bone pain adverse event C0206641 Osteochondromatosis OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0009404 Colorectal neoplasms HSDN C3887873 Hearing loss C0027643 Neoplasm recurrence, local HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0000771 Abnormalities, drug induced HSDN C0015230 Exanthem C0857236 Leg rash UMLS C0015469 Facial paralysis C0040053 Thrombosis HSDN C0019079 Bloody sputum C0037118 Silicotuberculosis HSDN C1961131 Cough adverse event C0205788 Histiocytoid hemangioma HSDN C0043094 Weight gain C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C3274924 Have been coughing C1963198 Pancreatitis adverse event HSDN C0851578 Disorder sleep C0027809 Neurilemmoma HSDN C3815497 Cough C0279628 Adenocarcinoma of esophagus OrphaNet C0035229 Respiratory function impaired C1864670 Neuronal ceroid lipofuscinosis, congenital OrphaNet|MalaCards C0557874 Global developmental delay C3810067 Congenital disorder of glycosylation, type ix MalaCards C4084768 Usual severity vomiting C0029456 Osteoporosis HSDN C3665492 Pigmentations C1621958 Glioblastoma multiforme MalaCards C0522224 Palsied C0024116 Lung diseases, fungal HSDN C0018681 Headache, cephalalgia C0750929 Arnold-chiari malformation, type i MalaCards C0037771 Paraparesis spastic C0268250 Gaucher disease, type 2 (disorder) MalaCards C0013604 Edematous C0027430 Nasal polyps HSDN C0221263 Cafe au lait spot C0553586 Cafe-au-lait macules with pulmonary stenosis MalaCards C4050613 Anxiety C0795907 Conotruncal anomaly face syndrome MalaCards|HPO C3815497 Cough C0014544 Epilepsy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0031094 Periodontal pocket HSDN C0004134 Dyssynergia C1970808 Xeroderma pigmentosum b-cockayne syndrome HPO C3641756 Have diarrhea C0018824 Heart valve disease HSDN C0030554 Abnormal sensation C0042384 Vasculitis HSDN C0518090 Frequency of pain question C0007124 Noninfiltrating intraductal carcinoma HSDN C4084802 Usual severity diarrhea C1833454 Komuragaeri disease MalaCards C0007758 Cerebellar ataxia C3541306 Plasmodium measurement HSDN C0007814 Cerebrospinal fluid otorrhea C0032019 Pituitary neoplasms HSDN C1963091 Diarrhea adverse event C0013374 Dysgammaglobulinemia HSDN C0850758 Pain pelvic C0037369 Smoking HSDN C0037763 Spasm C1553188 Hemolysis - observation HSDN C0010520 Skin cyanosis C0005411 Biliary atresia HSDN C4084773 Bothered by weight gain C0027627 Neoplasm metastasis HSDN C0026821 Cramp C0014550 Epilepsies, myoclonic HSDN C1262300 Decreased genital sensation C0549622 Sexual dysfunction UMLS C0242936 Center pain C0007856 Cervical rib syndrome HSDN C3463815 Feel fatigue C0003962 Ascites HSDN C1963167 Memory impairment adverse event C1843013 Alzheimer disease, familial, type 3 HPO C0234523 Apraxia, classic C0023522 Leukodystrophy, metachromatic HSDN C3539892 Pelvic pain in front C0236969 Substance-related disorders HSDN C1963281 Vomiting adverse event C0026785 Munchhausen syndrome HSDN C4085548 Usual severity dizziness C0162820 Dermatitis, allergic contact HSDN C1963071 Back pain adverse event C1444199 Alkaptonuric ochronosis MalaCards C0013132 Drooling C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C0004941 Behavioral symptoms C0035372 Rett syndrome OrphaNet C0007642 Cellulitis nos C2936739 Hyper-immunoglobulin e syndrome, autosomal dominant HPO C2024893 Cardiovascular surgery result: fatigue C1253943 Fluid in the chest HSDN C0027497 Queasy C0023896 Alcoholic liver diseases UMLS C4084774 Have weight loss C0041188 Pyomyositis, tropical OrphaNet|MalaCards C0700590 Diaphoresis excessive C0694549 Community acquired pneumonia UMLS C0011991 Loose stools C0151594 Hemorrhagic diarrhea UMLS C0000737 Abdomen pain C0242350 Erectile dysfunction HSDN C1384666 Decreased hearing C0042075 Urologic diseases HSDN C2237041 Shox gene with short stature C0268363 Osteogenesis imperfecta type iv (disorder) MalaCards|HPO C1510456 Wernicke aphasia C0162671 Melas syndrome HSDN C0235129 Feeling strange C1443060 Feeling abnormal UMLS C3463815 Feel fatigue C0020179 Huntington disease HSDN C2024893 Cardiovascular surgery result: fatigue C0017416 Genital neoplasms, female HSDN C0242936 Center pain C0585442 Osteosarcoma of bone HSDN C0004134 Dyssynergia C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0427055 Face weakness C1318518 Infantile malignant osteopetrosis MalaCards C4084776 Weight loss C1963088 Cystitis adverse event HSDN C0009676 Confusion state C1962963 Osteoporosis adverse event HSDN C4084775 Usual severity weight loss C0439840 Reflex motion descriptor HSDN C1549543 Administration method - pain C0085183 Neoplasms, second primary HSDN C1549543 Administration method - pain C0311375 Arsenic poisoning HSDN C1963252 Tremor adverse event C0022116 Ischemia HSDN C1971624 Appetite absent C0020517 Hypersensitivity HSDN C4084767 Bothered by vomiting C0034067 Pulmonary emphysema HSDN C4084768 Usual severity vomiting C0267830 Pyogenic liver abscess HSDN C0917801 Sleep disorder insomnia C1997249 Neuralgia, pudendal MalaCards C0700078 Deep tendon reflex decrease C1846367 Spinocerebellar ataxia 19 HPO C0042798 Vision dim C0024121 Lung neoplasms HSDN C0011206 Delirium acute C0007097 Carcinomas HSDN C1557397 Adverse event associated with pain C3809899 Episodic pain syndrome, familial, 3 MalaCards C0027066 Myoclonic jerking C0010674 Cystic fibrosis HSDN C0010520 Skin cyanosis C0011813 Dextrocardia HSDN C0027796 Neuralgias C0085096 Peripheral vascular diseases HSDN C0522224 Palsied C0016509 Dermatoses, foot HSDN C0018524 Hallucinate C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0454644 Delayed language development C4015710 Tenorio syndrome MalaCards C0038990 Sweats C0040028 Thrombocythemia, essential MalaCards C1145670 Failure respiratory C2931604 Ring 6, chromosome OrphaNet|MalaCards C4085210 Usual severity pain C0010418 Cryptosporidiosis HSDN C3463815 Feel fatigue C0011854 Diabetes mellitus, insulin-dependent HSDN C0015672 Decreased energy C0027809 Neurilemmoma HSDN C0018681 Headache, cephalalgia C0020443 Hypercholesterolemia HSDN C0019209 Large liver C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C1279888 Proteinuria of undiagnosed cause C0026896 Myasthenia gravis HSDN C0018834 Brash C1800706 Idiopathic pulmonary fibrosis MalaCards|HSDN C0002622 Amnesias C0011551 Depersonalisation HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1706377 Memory device component HSDN C0151786 Weakness muscle C0206660 Germinoma HSDN C0008031 Pain chest C0024236 Lymphedema HSDN C0028738 Nystagmus C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C0004134 Dyssynergia C0029132 Disorder of the optic nerve HSDN C0032285 Pneum C1865372 Athabaskan severe combined immunodeficiency HPO C0004604 Pain back C0039496 Temporomandibular joint dysfunction syndrome HSDN C1384666 Decreased hearing C1412750 Bbs5 gene HPO C0019521 Hiccoughs C0022738 Klippel-feil syndrome HSDN C2984058 Have pain C0520459 Necrotizing enterocolitis HSDN C4084802 Usual severity diarrhea C0021933 Intussusception HSDN C1963091 Diarrhea adverse event C0007117 Basal cell carcinoma HSDN C0497406 Over weight C0039006 Swine--diseases HSDN C0030552 Paralysis partial C1457883 Aggressive reaction HSDN C0015469 Facial paralysis C0001883 Airway obstruction HSDN C3829611 Nausea frequency C1411077 Ragpicker's disease MalaCards C0004134 Dyssynergia C1864840 Combined oxidative phosphorylation deficiency 3 MalaCards|HPO|UMLS C4084769 Vomiting frequency C0008924 Cleft lip HSDN C0917816 Deficiency mental C0751202 Cystathionine beta-synthase deficiency disease OrphaNet|HPO C0013604 Edematous C0595812 Fistula route HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0022660 Kidney failure, acute HSDN C3665492 Pigmentations C0346037 Acral lentiginous malignant melanoma MalaCards C0003079 Pupillary inequality C0025284 Meningeal neoplasms HSDN C0022346 Yellow skin C0206698 Cholangiocarcinoma OrphaNet|HSDN|HPO C4085549 Dizziness C0032371 Poliomyelitis HSDN C0004134 Dyssynergia C1847114 Spinocerebellar ataxia, autosomal recessive 5 OrphaNet|HPO C0030193 Sense of pain C0085605 Liver failure HSDN C1384666 Decreased hearing C0035455 Rhinitis HSDN C0002170 Alopecia disorders C1838256 Parc syndrome MalaCards C0033377 Caudal displacement C2931795 Chromosome 11, deletion 11p OrphaNet C0497247 Blood pressure elevation C1609433 Congenital absence of kidneys syndrome MalaCards|HPO C0749870 Upper motor neuron sign C1865409 Amyotrophic lateral sclerosis 4, juvenile MalaCards|UMLS C0270948 Neurogenic muscular atrophy C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards|HPO C0349588 Stature short C0265201 De sanctis-cacchione syndrome MalaCards C0002624 Amnesia retrograde C1579931 Depressed - symptom HSDN C4084726 Distress cough C0038525 Subarachnoid hemorrhage HSDN C3665386 Abnormal vision C3179239 Osteopetrosis autosomal dominant type 2 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0035220 Respiratory distress syndrome, newborn HSDN C1961131 Cough adverse event C0037939 Spinal neoplasms HSDN C0460137 Push down or depress C3665349 Secondary hypothyroidism OrphaNet C0000737 Abdomen pain C0085090 Lymphoma, aids-related MalaCards|HSDN C4085862 Bothered by nausea C0085693 Acute appendicitis nos (disorder) MalaCards C0016382 Cutaneous vascular engorgement C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C0234253 Rest pain C0042373 Vascular diseases UMLS C0004604 Pain back C0021845 Intestinal perforation HSDN C0086439 Activity decreased C0005944 Metabolic bone disorder HSDN C3665347 Vision impaired C0266539 Congenital total cataract MalaCards C4085549 Dizziness C0030499 Parasitic diseases HSDN C0015672 Decreased energy C0011168 Deglutition disorders HSDN|UMLS C1279888 Proteinuria of undiagnosed cause C0001621 Adrenal gland diseases HSDN C1963281 Vomiting adverse event C2937421 Prostatic hyperplasia HSDN C0030486 Extremity paralysis, lower C0007222 Cardiovascular diseases HSDN C4084773 Bothered by weight gain C0011389 Dental plaque HSDN C0013404 Respiratory difficulty C0004044 Asphyxia HSDN C0036572 Convulsion C3489393 Hiatal hernia HSDN C1963066 Joint pain adverse event C0019159 Hepatitis a DiseaseOntology|MalaCards C0003862 Pain joint C0007097 Carcinomas HSDN C0424755 Fever symptoms C0001175 Acquired immunodeficiency syndrome HSDN C0151786 Weakness muscle C0018671 Head and neck neoplasms HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0030920 Peptic ulcer HSDN C1962972 Proteinuria adverse event C0428478 Serum triglycerides raised HSDN C0013604 Edematous C0022739 Klippel-trenaunay-weber syndrome MalaCards C0000727 Abdomen acute C0007133 Carcinoma, papillary HSDN C0497247 Blood pressure elevation C2677362 Alveolar capillary dysplasia MalaCards C2984057 Have nausea C0026896 Myasthenia gravis HSDN C0009676 Confusion state C0024810 Marijuana smoking HSDN C4084802 Usual severity diarrhea C0850803 Anaphylaxis (non medication) HSDN C0027066 Myoclonic jerking C4015420 Epilepsy, progressive myoclonic 7 MalaCards|UMLS C0013404 Respiratory difficulty C2931347 Cardiac form of generalized glycogenosis MalaCards|HPO C2919142 Short stature adverse event C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C1963249 Tinnitus adverse event C0011581 Depressive disorder HSDN C3539893 Pelvic pain occurs with intercourse C0242669 Placenta retained HSDN C0333422 Gumma C0275852 Gumma of central nervous system nos UMLS C0039070 Collapse fleeting C1548777 Specimen reject reason - hemolysis HSDN C0007758 Cerebellar ataxia C1859565 Bardet-biedl syndrome 7 HPO C4084726 Distress cough C0001580 Adolescent behavior HSDN C1000483 Genus anemia C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C0013604 Edematous C1963229 Retinal detachment adverse event HSDN C0042024 Urine incontinence C0006109 Brain damage, chronic HSDN C4085661 Usual severity nausea C0027809 Neurilemmoma HSDN C1963067 Atrial fibrillation adverse event C1865019 Short qt syndrome 2 (disorder) MalaCards|HPO C0522224 Palsied C0041582 Ulcer HSDN C0042963 Symptoms vomiting C0016658 Fracture bone HSDN C3539889 Pelvic pain increasing in severity C0014179 Endometritis HSDN C0018784 Deafness sensorineural C0021053 Immune system diseases HSDN C0018991 Paralysis one side of body C0009938 Bruising HSDN C4084802 Usual severity diarrhea C0010631 Cystadenocarcinoma HSDN C1963184 Nystagmus adverse event C1859565 Bardet-biedl syndrome 7 HPO C1963281 Vomiting adverse event C0206255 Malaria vaccine HSDN C4084769 Vomiting frequency C0026598 Movement perception HSDN C0000727 Abdomen acute C0026766 Multiple organ failure HSDN C0019572 Hairiness C0040136 Thyroid neoplasm HSDN C0012569 Double vision C0152276 Granulocytic sarcoma HSDN C4085211 Pain distress question C0005686 Urinary bladder diseases HSDN C1557397 Adverse event associated with pain C0043167 Pertussis HSDN C0039070 Collapse fleeting C0795868 Chromosome 18, tetrasomy 18p MalaCards C0349588 Stature short C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C1963087 Constipation adverse event C1838569 Caudal dysgenesis syndrome HPO C0033377 Caudal displacement C0029089 Ophthalmoplegia MalaCards C0040822 D tremors C0376329 New variant creutzfeldt-jakob disease MalaCards C0028738 Nystagmus C4024961 Metachromatic leukodystrophy variant MalaCards C4085210 Usual severity pain C0040435 Tooth diseases HSDN C0027066 Myoclonic jerking C0003864 Arthritis HSDN C2203646 Jaundice C0040560 Toxoplasmosis, congenital MalaCards|HSDN C2242996 Tingling C0037650 Somatoform disorder HSDN C0042963 Symptoms vomiting C1961100 Erectile dysfunction adverse event HSDN C0013362 Dysarthrias C0038868 Progressive supranuclear palsy HPO C1519353 Skin eruption papular C2973529 Leukocytoclastic vasculitis MalaCards C0042798 Vision dim C3151202 Leber congenital amaurosis 8 MalaCards|HPO C0030232 Color loss C1861848 Paragangliomas 4 MalaCards C0030794 Pelvis pain C1456865 Ureteral calculi HSDN C2203646 Jaundice C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0000737 Abdomen pain C1514428 Primary peritoneal carcinoma MalaCards C0004093 Asthenia C0009946 Conversion disorder HSDN C0037384 Snore C0024636 Malocclusion HSDN C4084774 Have weight loss C1963215 Pneumothorax adverse event HSDN C4085317 Diarrhea frequency C1862892 Hereditary angioedema type ii HPO C4084724 Usual severity constipation C0518449 Control of hip fracture risk HSDN C0151889 Reflexes tendon increased C1858712 Spastic paraplegia 10, autosomal dominant MalaCards|HPO C3463815 Feel fatigue C0034365 Q-sort HSDN C0024031 Back pain lower back C0158252 Intervertebral disc disorder UMLS C0026205 Pupillary constriction C0034119 Punishment HSDN C1384666 Decreased hearing C0019348 Herpes simplex infections HSDN C0042963 Symptoms vomiting C0032266 Emphysema, intestinal HSDN C2237041 Shox gene with short stature C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C2984058 Have pain C0030804 Pemphigoid, benign mucous membrane HSDN C2315100 Pediatric failure to thrive C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|HPO|MalaCards C0042798 Vision dim C0037274 Dermatologic disorders HSDN C1963091 Diarrhea adverse event C0025267 Multiple endocrine neoplasia type 1 OrphaNet|HPO C4085549 Dizziness C0314657 Genetic predisposition HSDN C1279888 Proteinuria of undiagnosed cause C0948480 Coronary restenosis HSDN C1961131 Cough adverse event C0796561 Melanoma vaccines HSDN C0030552 Paralysis partial C0009404 Colorectal neoplasms HSDN C3463815 Feel fatigue C0238027 Botulism, infantile MalaCards C1000483 Genus anemia C0001768 Agammaglobulinemia MalaCards C4084727 Cough frequency C0149721 Left ventricular hypertrophy HSDN C0151786 Weakness muscle C0006261 Bronchial diseases HSDN C0020305 Fetal edema C0024507 Majewski syndrome MalaCards|HPO C0917816 Deficiency mental C0546966 Monilethrix MalaCards|HPO C4084724 Usual severity constipation C1258104 Diffuse scleroderma HSDN C0242936 Center pain C1720887 Female urogenital diseases HSDN C0008031 Pain chest C0004238 Atrial fibrillation UMLS C4084788 Have dizziness C0024904 Mastoiditis HSDN C1963252 Tremor adverse event C1548578 Location characteristic id - smoking HSDN C4085661 Usual severity nausea C0276786 Human balantidiasis MalaCards C4085222 Nausea C0036916 Sexually transmitted diseases HSDN C3539020 Pelvic pain decreasing in frequency C0036864 Sexual relations HSDN C0162298 Stiffness joints C1859711 Arthrogryposis multiplex congenita with whistling face OrphaNet|MalaCards C0332563 Papulae C1836122 Sarcoidosis, early-onset MalaCards C1961131 Cough adverse event C0038454 Cerebrovascular accident HSDN C3641756 Have diarrhea C0001621 Adrenal gland diseases HSDN C1963091 Diarrhea adverse event C0021070 Immunoproliferative disease HSDN C0221232 Welts C0578870 Chronic spontaneous urticaria UMLS C0031911 Pigment deposition C0339535 Night blindness, congenital stationary MalaCards C0028738 Nystagmus C0342777 Succinate-coenzyme q reductase deficiency MalaCards C4084726 Distress cough C0343528 Legionella pneumophila; infection, nonpneumonic OrphaNet|MalaCards C0424755 Fever symptoms C0037116 Silicosis HSDN C0027796 Neuralgias C0039483 Giant cell arteritis HSDN C0043094 Weight gain C0001349 Acute-phase reaction HSDN C1557397 Adverse event associated with pain C0162309 Adrenoleukodystrophy HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003855 Arteriovenous fistula HSDN C0518090 Frequency of pain question C0005686 Urinary bladder diseases HSDN C0557874 Global developmental delay C1845050 Pigmentary disorder, reticulate, with systemic manifestations HPO C0424755 Fever symptoms C0282687 Hemorrhagic fever, ebola DiseaseOntology|HSDN|OrphaNet|MalaCards C0015970 Fever unknown origin C0034040 Puerperal disorders HSDN C0020672 Body temperature decreased C0027932 Neurotic disorders HSDN C0917816 Deficiency mental C0265374 Warfarin syndrome OrphaNet|MalaCards C1069915 Vertigo C2717757 Retinocochleocerebral vasculopathies MalaCards C2017373 Right leg soft tissue swelling with black and blue discoloration C0037580 Soft tissue swelling UMLS C0015468 Face pain C1963067 Atrial fibrillation adverse event HSDN C0150055 Pain chronic C2074900 Chronic postoperative pain UMLS C0009806 Constipate C0305062 Tetanus toxoids HSDN C2024878 Cardiovascular surgery result: dyspnea C0009373 Colonic diseases HSDN C0018681 Headache, cephalalgia C1332189 Adult brain meningioma UMLS C0018784 Deafness sensorineural C0035091 Renal tubular transport, inborn errors HSDN C2911647 Weight gain adverse event C0027726 Nephrotic syndrome HSDN C4084767 Bothered by vomiting C1956346 Coronary artery disease HSDN C2024893 Cardiovascular surgery result: fatigue C0001403 Addison disease OrphaNet C0270948 Neurogenic muscular atrophy C0022541 Kearns-sayre syndrome OrphaNet|HPO|MalaCards C2984057 Have nausea C0010674 Cystic fibrosis HSDN C2025995 Cellulitis C0015773 Felty syndrome MalaCards C4084802 Usual severity diarrhea C3665596 Warts HSDN C0002965 Crescendo angina C0342257 Complications of diabetes mellitus HSDN C4085862 Bothered by nausea C0038579 Substance abuse, intravenous HSDN C0013404 Respiratory difficulty C0347555 Friction blister HSDN C1963252 Tremor adverse event C1837454 Spinocerebellar ataxia 8 MalaCards|HPO C1384666 Decreased hearing C0750929 Arnold-chiari malformation, type i MalaCards C0042024 Urine incontinence C0024117 Chronic obstructive airway disease HSDN C4084725 Usual severity cough C0001519 Adie holmes syndrome HSDN C0557874 Global developmental delay C0268540 Hhh syndrome HPO C0005745 Blepharoptosis C1833835 Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency MalaCards C0027497 Queasy C0233629 Thinking and speaking disturbances HSDN C0454644 Delayed language development C0205711 Pelizaeus-merzbacher disease MalaCards|HPO C4084769 Vomiting frequency C0085423 Gram-negative bacterial infections HSDN C0030193 Sense of pain C0032302 Mycoplasma pneumonia HSDN C3641756 Have diarrhea C0149514 Bronchitis acute HSDN C0036572 Convulsion C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C2911647 Weight gain adverse event C0011311 Dengue fever HSDN C0027796 Neuralgias C0524909 Hepatitis b, chronic HSDN C0349588 Stature short C0342200 Endemic cretinism MalaCards C0000727 Abdomen acute C0038356 Stomach neoplasms HSDN C4084724 Usual severity constipation C0005586 Bipolar disorder HSDN C4084775 Usual severity weight loss C1527406 Rhizomelic pseudopolyarthritis MalaCards C0043094 Weight gain C0020557 Hypertriglyceridemia HSDN C3641755 Have constipation C0268322 Chester-type porphyria HPO C0018772 Deafness C1859568 Bardet-biedl syndrome 10 HPO C4084723 Constipation C0029408 Degenerative polyarthritis HSDN C4084726 Distress cough C0038454 Cerebrovascular accident HSDN C2984058 Have pain C0005686 Urinary bladder diseases HSDN C0241210 Speaking delay C3150923 Mental retardation with language impairment and autistic features HPO C1549543 Administration method - pain C0029295 Oropharyngeal neoplasms HSDN C4084784 Diarrhea C0206172 Diabetic foot HSDN C0023012 Delay language C2930926 Autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes MalaCards C3898969 Have been vomiting C0020443 Hypercholesterolemia HSDN C4085862 Bothered by nausea C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C4084788 Have dizziness C0004303 Auditory disease, central HSDN C0349588 Stature short C1832615 Hyperparathyroidism, neonatal severe OrphaNet|HPO C4085661 Usual severity nausea C0162576 Anisakiasis MalaCards C0151786 Weakness muscle C0027666 Neoplasms, radiation-induced HSDN C3898969 Have been vomiting C0162666 Mitochondrial encephalomyopathies HSDN C3815497 Cough C1956390 Cranial arteritis MalaCards C0917816 Deficiency mental C1866504 Photosensitive trichothiodystrophy MalaCards|HPO C0426579 Anorexia symptom C0038271 Stereotyped behavior HSDN C2032395 Pelvic pain on the left C1456865 Ureteral calculi HSDN C0349588 Stature short C2673861 Camptodactyly syndrome, guadalajara, type ii OrphaNet|MalaCards C0018834 Brash C1998602 Meals HSDN C0011175 Deficient fluid volume C1866495 Bartter syndrome, antenatal type 1 HPO C0917816 Deficiency mental C4015357 Mental retardation, autosomal dominant 31 MalaCards C3274924 Have been coughing C1546949 Event consequence - death HSDN C0040822 D tremors C0265499 49,xxxxy chromosomal anomaly MalaCards C2984058 Have pain C0024440 Macular edema, cystoid HSDN C0349588 Stature short C0268243 Niemann-pick disease, type b MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0008533 Hemophilia b HSDN C0017181 Gastrointestinal bleed C0033847 Pseudoxanthoma elasticum MalaCards|HPO C0035078 Failure kidney C1840333 Barakat syndrome OrphaNet|HPO C0041657 Consciousness loss C0014068 Encephalomalacia HSDN C2024893 Cardiovascular surgery result: fatigue C0035078 Kidney failure HSDN C0000737 Abdomen pain C3489393 Hiatal hernia HSDN C0005745 Blepharoptosis C0346303 Thyrotroph adenoma MalaCards C4084784 Diarrhea C0018916 Hemangioma HSDN C0022346 Yellow skin C4225390 Bile acid synthesis defect, congenital, 5 UMLS C0005745 Blepharoptosis C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C2047434 Hyperemesis gravidarum in second half of pregnancy with baby delivered C0156699 Late preg.vomiting unspecif. UMLS C0040485 Wryneck C3489393 Hiatal hernia HSDN C0004604 Pain back C0011603 Dermatitis HSDN C2984057 Have nausea C1855652 Fetus small for gestational age HSDN C1069915 Vertigo C0003490 Aortic arch syndrome HSDN C1860844 Sparse, thin hair C0587248 Costello syndrome (disorder) MalaCards|HPO C4084724 Usual severity constipation C0729582 Floating-harbor syndrome OrphaNet|HPO|MalaCards C0020305 Fetal edema C0040587 Mounier kuhn syndrome HSDN C0241210 Speaking delay C1846055 Siderius x-linked mental retardation syndrome MalaCards C0221263 Cafe au lait spot C0015625 Fanconi anemia MalaCards|HPO C0018784 Deafness sensorineural C1850626 Nathalie syndrome OrphaNet|MalaCards C4084802 Usual severity diarrhea C1762616 Meningioma, benign, no icd-o subtype HSDN C0039070 Collapse fleeting C0037274 Dermatologic disorders HSDN C4084726 Distress cough C1955864 Cardiac sinus arrest HSDN C0030975 Disorders perception C3714514 Infection HSDN C0015230 Exanthem C0302295 Eruptions UMLS C0009421 Comatose C0037929 Spinal cord injuries HSDN C2984058 Have pain C0007856 Cervical rib syndrome HSDN C0020615 Hypoglycemia nos C0342573 Pituitary dwarfism i HPO C0030193 Sense of pain C0950123 Inborn genetic disease HSDN C0349588 Stature short C3809007 Cardiofaciocutaneous syndrome 4 MalaCards C0018681 Headache, cephalalgia C0005874 Blushing HSDN C0424755 Fever symptoms C0007621 Neoplastic cell transformation HSDN C2203646 Jaundice C2608083 Cholestasis, benign recurrent intrahepatic 2 MalaCards|HPO C0155552 Hearing loss mixed C0265354 Charge syndrome MalaCards|HPO C0391860 Diffuse inflammations C1277259 Pangastritis UMLS C0013362 Dysarthrias C0206042 Fatal familial insomnia HPO C0518090 Frequency of pain question C0037304 Skull fracture HSDN C4084788 Have dizziness C0036095 Salivary gland neoplasms HSDN C4084802 Usual severity diarrhea C0010481 Cushing syndrome HSDN C0027497 Queasy C2586211 Thrombosis of blood vessel HSDN C0042024 Urine incontinence C0029410 Osteoarthritis of hip HSDN C0242936 Center pain C0038663 Suicide attempt HSDN C1836296 Lower extremity weakness C1334698 Meningothelial cell neoplasm MalaCards C0030554 Abnormal sensation C0042029 Urinary tract infection HSDN C0020455 Hypergammaglobulinemia C0343084 Capillary leak syndrome HSDN C0009421 Comatose C2984291 Glioblastoma multiforme pathway HSDN C1279888 Proteinuria of undiagnosed cause C0036916 Sexually transmitted diseases HSDN C3887638 Failure to thrive in infant C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C0042024 Urine incontinence C1334698 Meningothelial cell neoplasm MalaCards C3539020 Pelvic pain decreasing in frequency C0002871 Anemia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0524620 Metabolic syndrome x HSDN C0000737 Abdomen pain C0861856 Bile duct colloid carcinoma UMLS C0013395 Indigestion C1546949 Event consequence - death HSDN C0242936 Center pain C0040443 Avulsed tooth HSDN C0013404 Respiratory difficulty C1848814 Thymoma, familial MalaCards C0009421 Comatose C0206255 Malaria vaccine HSDN C0018772 Deafness C1000587 Pemphigus HSDN C2237041 Shox gene with short stature C1845862 Creatine deficiency, x-linked OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0003175 Anthrax disease HSDN C0850758 Pain pelvic C0019270 Hernia HSDN C2024893 Cardiovascular surgery result: fatigue C0037579 Soft tissue neoplasms HSDN C4085862 Bothered by nausea C0243026 Sepsis HSDN C3541349 Syncope C0019829 Hodgkin disease HSDN C1963093 Dizziness adverse event C0027643 Neoplasm recurrence, local HSDN C0004604 Pain back C0001430 Adenoma HSDN C2984057 Have nausea C0014175 Endometriosis HSDN C0917816 Deficiency mental C1844865 Charcot-marie-tooth disease, x-linked recessive, 3 (disorder) OrphaNet C0018834 Brash C0010068 Coronary heart disease HSDN C2984057 Have nausea C0848377 Trauma to the abdomen HSDN C0393903 Leg moving painful toe C0598106 Encephalomyelopathies UMLS C0030554 Abnormal sensation C0035126 Reperfusion injury HSDN C0016204 Fart C3489393 Hiatal hernia HSDN C0036659 Sensation disorder C0034734 Raynaud disease HSDN C3887873 Hearing loss C3539923 Cdisc adas-cog - orientation summary score HSDN C2984058 Have pain C2350521 Gustatory perception HSDN C0011991 Loose stools C0026590 Child mother relationship HSDN C0036572 Convulsion C1836123 Goldberg-shprintzen megacolon syndrome HPO C2984058 Have pain C0243001 Abdominal abscess HSDN C0013404 Respiratory difficulty C0796070 Microphthalmia, syndromic 7 MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0030290 Fistula pancreatic HSDN C0427055 Face weakness C1867983 Porencephaly, familial UMLS C0042798 Vision dim C1848172 Night blindness, congenital stationary, type 2a HPO C2919142 Short stature adverse event C3541319 Short stature, optic nerve atrophy, and pelger-huet anomaly MalaCards C1557397 Adverse event associated with pain C0014511 Epithelial cyst HSDN C0004604 Pain back C1709781 Pyothorax-associated lymphoma UMLS C0019825 Voice hoarseness C0030521 Parathyroid neoplasms MalaCards C0241165 Skin thickening C1846171 Lissencephaly, x-linked, 2 MalaCards C0857305 Thrombocytopenia purpura C2984289 Melanoma pathway HSDN C0242936 Center pain C0919691 Anastomotic leaks HSDN C0042571 Vertigo subjective C0033871 Psychiatric status rating scales HSDN C0018777 Deafness, conductive C0009363 Congenital ocular coloboma (disorder) HSDN C3665347 Vision impaired C3809464 Myopia 22, autosomal dominant MalaCards C0018681 Headache, cephalalgia C0149721 Left ventricular hypertrophy HSDN C0557874 Global developmental delay C3810225 Mental retardation, autosomal recessive 41 MalaCards C0242936 Center pain C2028283 History of premature birth HSDN C0038002 Spleen enlargement C0002016 Aleutian mink disease DiseaseOntology|MalaCards C0026858 Musculoskeletal pain C0019693 Hiv infections HSDN C0575081 Abnormal gait C0751783 Lafora disease HPO C0039070 Collapse fleeting C0004935 Animal ethology HSDN C4084725 Usual severity cough C0024214 Lymphangiectasis HSDN C0019521 Hiccoughs C0018920 Hemangioma, cavernous HSDN C4085211 Pain distress question C0025149 Medulloblastoma HSDN C0011991 Loose stools C0003864 Arthritis HSDN C0231341 Aging premature C0002395 Alzheimer's disease HSDN C2911647 Weight gain adverse event C0043241 Wound infection HSDN C4084769 Vomiting frequency C0022658 Kidney diseases HSDN C0151786 Weakness muscle C0265294 Pyle metaphyseal dysplasia MalaCards|HPO|UMLS C0917816 Deficiency mental C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0221263 Cafe au lait spot C0015461 Facial neoplasms HSDN C4084726 Distress cough C0276119 Q-fever pneumonia MalaCards C4084769 Vomiting frequency C0001580 Adolescent behavior HSDN C0007166 Cardiac output decreased C4085311 Depression - recess HSDN C0036572 Convulsion C0268262 Metachromatic leukodystrophy due to saposin b deficiency HPO|UMLS C1963184 Nystagmus adverse event C1849096 Infantile onset spinocerebellar ataxia MalaCards|HPO C0023380 Lethargy C1864912 2-methylbutyryl-coa dehydrogenase deficiency HPO|UMLS C0857305 Thrombocytopenia purpura C0019699 Hiv seropositivity HSDN C0424755 Fever symptoms C2350521 Gustatory perception HSDN C0030794 Pelvis pain C0409354 Flexion contracture of hip HSDN C0740961 Amputation stump pain C0302473 Amputation stump; complications UMLS C0454644 Delayed language development C1859565 Bardet-biedl syndrome 7 HPO C0522067 Hepatic pain C2017951 Special symptoms or syndromes, not elsewhere classified in medcin UMLS C0015230 Exanthem C0585274 Periodic syndrome HPO C4085317 Diarrhea frequency C0030807 Pemphigus, nos HSDN C0031911 Pigment deposition C0027766 Nervous system neoplasms MalaCards C3539890 Pelvic pain causes awakening at night C0037369 Smoking HSDN C0917801 Sleep disorder insomnia C0868777 Persistent disorder of initiating or maintaining sleep UMLS C0020438 Hypercalciuria C0362046 Prediabetes syndrome HSDN C0018808 Murmur C0162872 Aortic aneurysm, thoracic HSDN C1962957 Flushing adverse event C0085257 Yin deficiency HSDN C0018926 Emesis bloody C3244301 Coverage level - family HSDN C0030193 Sense of pain C0011586 Three dimensional vision HSDN C1384666 Decreased hearing C0520946 Emotional hypersensitivity HSDN C0030193 Sense of pain C0003460 Anurias HSDN C3146279 Coma C0027531 Neck injury HSDN C0013604 Edematous C2609414 Acute kidney injury HSDN C0233565 Bradykinesia C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO|UMLS C0015469 Facial paralysis C0270969 Zebra body myopathy OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0035229 Respiratory insufficiency HSDN C0018926 Emesis bloody C0035613 Rift valley fever MalaCards C0085631 Abnormal excitement C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0019825 Voice hoarseness C0036413 Scleredema adultorum HSDN C0026858 Musculoskeletal pain C0025239 Melorheostosis HSDN C0270790 Quadriparesis C1290877 Extremities disorders UMLS C4084767 Bothered by vomiting C0017160 Gastroenteritis DiseaseOntology C0007859 Pain neck C0036690 Septicemia HSDN C4085317 Diarrhea frequency C0002940 Aneurysm HSDN C0007758 Cerebellar ataxia C3807295 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant MalaCards|UMLS C4085548 Usual severity dizziness C0018798 Congenital heart defects HSDN C0023015 Language handicap C0039538 Teratoma HSDN C0000737 Abdomen pain C0264743 Rheumatic fever without heart involvement MalaCards C0028081 Night sweat C0854811 Refractory hodgkin's disease lymphocyte depleted UMLS C0518090 Frequency of pain question C0019087 Hemorrhagic disorders HSDN C0013144 Drowsy C0153066 Murray valley encephalitis DiseaseOntology|MalaCards C0015970 Fever unknown origin C1548578 Location characteristic id - smoking HSDN C1557397 Adverse event associated with pain C0040761 Transposition of great vessels HSDN C0026838 Spasticity muscle C1579931 Depressed - symptom HSDN C4084802 Usual severity diarrhea C0678202 Granulomatous enteritis MalaCards C1963071 Back pain adverse event C0010054 Coronary arteriosclerosis HSDN C1279888 Proteinuria of undiagnosed cause C0034067 Pulmonary emphysema HSDN C4084768 Usual severity vomiting C0004943 Behcet syndrome HSDN C0019209 Large liver C1836797 Combined oxidative phosphorylation deficiency 1 MalaCards|HPO C2037131 Nasal visual field defects in both eyes, sudden onset C0271202 Hemianopsia homonymous UMLS C0018681 Headache, cephalalgia C1334970 Medulloblastoma with extensive nodularity UMLS C0027497 Queasy C0008925 Cleft palate HSDN C2919142 Short stature adverse event C3809431 Microcephaly 11, primary, autosomal recessive MalaCards C0030552 Paralysis partial C0040156 Thyrotoxicosis MalaCards|HSDN C0036572 Convulsion C0007684 Central nervous system infection HSDN C4085211 Pain distress question C0868910 Oligozoospermia HSDN C0424755 Fever symptoms C0011603 Dermatitis HSDN C0424755 Fever symptoms C3163620 Hypotension adverse event HSDN C0009676 Confusion state C1546847 Entity name part type - family HSDN C0030193 Sense of pain C0347095 Carcinoma in situ of nasal cavity, nos UMLS C0026838 Spasticity muscle C0003803 Arnold chiari malformation MalaCards C0036572 Convulsion C2986768 Injected dose HSDN C4084769 Vomiting frequency C0040997 Trigeminal neuralgia HSDN C3887638 Failure to thrive in infant C0342737 3-hydroxyisobutyric aciduria MalaCards C4084723 Constipation C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease OrphaNet|HPO C0020672 Body temperature decreased C0036983 Septic shock HSDN C0030552 Paralysis partial C0002395 Alzheimer's disease HSDN C0022346 Yellow skin C0032229 Pleural neoplasms HSDN C0040822 D tremors C0039128 Syphilis HSDN C3539892 Pelvic pain in front C0019310 Hernia, obturator HSDN C0178417 Anhedonia C0009240 Cognition HSDN C1963071 Back pain adverse event C0032914 Pre-eclampsia HSDN C0007758 Cerebellar ataxia C4275170 Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 UMLS C0013604 Edematous C0003794 Arm injury HSDN C0522224 Palsied C0016542 Foreign body HSDN C2108107 Continuous electrocardiogram sinus bradycardia C1970119 Cardiac arrhythmia, ankyrin-b-related MalaCards|HPO C4085549 Dizziness C0018213 Graves disease HSDN C0039870 Leanness C0036357 Psychology, schizophrenic HSDN C0270948 Neurogenic muscular atrophy C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) MalaCards C0009792 Consciousness disorder C0338586 Vertebral artery dissection HSDN C0036659 Sensation disorder C0037773 Spastic paraplegia, hereditary HSDN C1579931 Depressed - symptom C0022336 Creutzfeldt-jakob disease MalaCards|HPO C0426579 Anorexia symptom C0003811 Cardiac arrhythmia HSDN C0242936 Center pain C0007789 Cerebral palsy HSDN C1963170 Hypothermia adverse event C0428953 Ecg infarction myocardial HSDN C0000737 Abdomen pain C0877572 Ovarian serous cystadenofibroma UMLS C0557874 Global developmental delay C1850343 Mosaic variegated aneuploidy syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C0026896 Myasthenia gravis HSDN C0151889 Reflexes tendon increased C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C0035229 Respiratory function impaired C2931196 Craniofacial dysostosis type 1 MalaCards C0020505 Excessive eating C0014859 Esophageal neoplasms HSDN C0013395 Indigestion C1266026 Gastric parietal cell adenocarcinoma UMLS C0231218 Malaise generalized C1336208 Stage iiia carcinoma of liver cells UMLS C0009806 Constipate C0022758 Kap HSDN C0011168 Disorder deglutition C0154682 Lateral sclerosis MalaCards C0349588 Stature short C1968740 Glycogen storage disease iiib HPO C4085211 Pain distress question C0039520 Tenosynovitis HSDN C0349489 Fetal hypoxia C0003128 Anovulation HSDN C3146279 Coma C0342728 3-methylglutaconic aciduria type 1 MalaCards|HPO C0151818 Opisthotonos C1854990 Molybdenum cofactor deficiency, complementation group c HPO C0000737 Abdomen pain C2987166 Pancreatic medullary carcinoma UMLS C0036572 Convulsion C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C3463815 Feel fatigue C0024899 Mastocytosis MalaCards C2024893 Cardiovascular surgery result: fatigue C0024141 Lupus erythematosus, systemic HSDN C0086439 Activity decreased C0004442 Avoidance learning HSDN C0034150 Skin purpura C0015695 Fatty liver HSDN C4085210 Usual severity pain C0033871 Psychiatric status rating scales HSDN C0040259 Tinea pedis C0034212 Pyoderma HSDN C0000737 Abdomen pain C0007621 Neoplastic cell transformation HSDN C2315100 Pediatric failure to thrive C2750785 Muscular dystrophy, congenital, lmna-related (disorder) HPO C4084802 Usual severity diarrhea C0242550 Behavior, risk reduction HSDN C0030232 Color loss C0024419 Waldenstrom macroglobulinemia OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C2675644 Niemann-pick disease, intermediate, with visceral involvement and rapid progression HPO C0028738 Nystagmus C0555206 Chiari malformation type ii MalaCards C0020538 Hbp C1864851 Pigmented nodular adrenocortical disease, primary, 2 MalaCards|HPO C1959630 Eye pain adverse event C0751815 Carotid artery, internal, dissection HSDN C1557397 Adverse event associated with pain C0038271 Stereotyped behavior HSDN C0002170 Alopecia disorders C1832593 Alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism MalaCards C0155552 Hearing loss mixed C0031997 Perception, pitch HSDN C4084788 Have dizziness C0752140 Intracranial embolism HSDN C0010200 Cough symptom C0018133 Graft-vs-host disease HSDN C4084769 Vomiting frequency C0853697 Neutrophil count decreased HSDN C4042891 Sleep wake disorders C0004442 Avoidance learning HSDN C4085210 Usual severity pain C0013289 Duodenal diseases HSDN C1963064 Anxiety adverse event C0796135 Renpenning syndrome 1 HPO C0003862 Pain joint C3536983 Familial hypophosphatemic rickets MalaCards|HSDN C0002962 Angina C0029295 Oropharyngeal neoplasms HSDN C3665347 Vision impaired C0268360 Osteogenesis imperfecta, recessive perinatal lethal OrphaNet C1963091 Diarrhea adverse event C0023241 Legionnaires' disease MalaCards C0557874 Global developmental delay C2931325 Chromosome 22 ring MalaCards C4085661 Usual severity nausea C0037313 Sleep HSDN C0042798 Vision dim C0035321 Retinal tear HSDN C1963274 Vasculitis adverse event C0014804 Erythromelalgia MalaCards|HPO C0013421 Dystonia C1962979 Burn adverse event HSDN C2936821 Spinal cerebrospinal fluid leak C0206731 Angiofibroma HSDN C4084784 Diarrhea C0026780 Mumps HSDN C0424755 Fever symptoms C0037926 Compression of spinal cord HSDN C3665346 Loss sight C1849112 Spastic quadriplegia-retinitis pigmentosa-mental retardation syndrome MalaCards C2984058 Have pain C0018995 Hemochromatosis HSDN C3641755 Have constipation C0033775 Anal pruritus HSDN C2237041 Shox gene with short stature C0406704 Rudiger syndrome 1 HPO C1963091 Diarrhea adverse event C0036674 Sensory deprivation HSDN C4084774 Have weight loss C0041234 Chagas disease HSDN C0002962 Angina C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0012833 Dizzy C0018213 Graves disease HSDN C0151889 Reflexes tendon increased C0751276 Metachromatic leukodystrophy, juvenile type HPO C0007859 Pain neck C1556682 Adverse event associated with infection HSDN C1963281 Vomiting adverse event C3241945 Melena due to gastrointestinal hemorrhage HSDN C0030552 Paralysis partial C1548484 Rheumatic fever vaccine HSDN C0020796 Profoundly mentally retarded C1850055 Peho syndrome MalaCards|HPO C0233794 Memory impaired C2960129 Vanishing white matter disease MalaCards C0020458 Hyperhydrosis C0751919 Acquired neuromyotonia OrphaNet|MalaCards C0018524 Hallucinate C0023895 Liver diseases HSDN C0349588 Stature short C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C0850758 Pain pelvic C0227791 Discharge vaginal HSDN C1962956 Flatulence adverse event C0024121 Lung neoplasms HSDN C3463815 Feel fatigue C2936917 Infantile polyarteritis MalaCards C4084724 Usual severity constipation C0013502 Echinococcosis HSDN C0241165 Skin thickening C0265313 Weill-marchesani syndrome OrphaNet|HPO|MalaCards C0233514 Behavior abnormal C2931816 Chromosome 2, monosomy 2q24 OrphaNet|MalaCards C0027066 Myoclonic jerking C0037926 Compression of spinal cord HSDN C0001707 Aerophagia C1701940 Pneumonia, ventilator-associated HSDN C3898969 Have been vomiting C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C3641755 Have constipation C0795623 Hepatitis a vaccine, inactivated HSDN C0518090 Frequency of pain question C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse HSDN C0234146 Absent reflex C1842197 Charcot-marie-tooth disease, recessive intermediate a HPO C0460137 Push down or depress C1856493 Gaucher disease, norrbottnian type HPO C0036572 Convulsion C4014538 Helsmoortel-van der aa syndrome MalaCards C1384666 Decreased hearing C0009375 Colonic neoplasms HSDN C3274920 Have shortness of breath question C0085129 Bronchial hyperreactivity MalaCards C0000737 Abdomen pain C4045991 Perihilar cholangiocarcinoma MalaCards C4084774 Have weight loss C0004364 Autoimmune diseases HSDN C0019572 Hairiness C2751321 Macrocephaly, alopecia, cutis laxa, and scoliosis OrphaNet|HPO C3274924 Have been coughing C0007138 Carcinoma, transitional cell HSDN C0231528 Muscle pain generalized C2673198 Familial cold autoinflammatory syndrome 2 MalaCards|HPO C0024032 Birth weight subnormal C1857553 Hsd11b2, arg208cys HPO C0424755 Fever symptoms C0032851 Disease poultry HSDN C0030200 Intractable pain C0149697 Foot injury wound nos HSDN C0026961 Pupil dilated C3151201 Multisystemic smooth muscle dysfunction syndrome MalaCards|HPO C0011991 Loose stools C0027439 Nasopharyngeal neoplasms HSDN C1384666 Decreased hearing C3150928 Nf1 microdeletion syndrome MalaCards C1963063 Anorexia adverse event C0595888 Phosphate serum decreased HSDN C0002963 Angina variant C3178805 Heterotaxy syndrome HSDN C0424755 Fever symptoms C1690964 Cataract HSDN C1963087 Constipation adverse event C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C2984057 Have nausea C0151744 Myocardial ischemia HSDN C0040485 Wryneck C0014474 Ependymoma HSDN C4085211 Pain distress question C0376545 Hematologic neoplasms HSDN C0029163 Hemorrhage mouth C0027651 Tumor HSDN C0398650 Idiopathic thrombocytopenia purpura C3553512 Immunodeficiency, common variable, 8, with autoimmunity MalaCards C0036396 Sciatica C0585052 Chronic sciatica UMLS C0150055 Pain chronic C0042138 Uterine neoplasms HSDN C0151686 Growth retardation C1854990 Molybdenum cofactor deficiency, complementation group c HPO C0036572 Convulsion C2931705 Chromosome 15, distal trisomy 15q OrphaNet|MalaCards C1069915 Vertigo C0029883 Otitis media with effusion HSDN C0000737 Abdomen pain C1261473 Sarcoma HSDN C0851578 Disorder sleep C0033936 Psychoses, alcoholic HSDN C0015672 Decreased energy C0004030 Aspergillosis HSDN C0917816 Deficiency mental C1706192 Sulfatidosis MalaCards C0042571 Vertigo subjective C0162820 Dermatitis, allergic contact HSDN C3539890 Pelvic pain causes awakening at night C0520720 Cyst nerve root HSDN C0015672 Decreased energy C0038160 Staphylococcal infections HSDN C3829611 Nausea frequency C0043528 Zoonoses HSDN C2024893 Cardiovascular surgery result: fatigue C0032927 Precancerous conditions HSDN C0030193 Sense of pain C0042487 Venous thrombosis HSDN C0427055 Face weakness C1263858 Muscular dystrophy congenital, merosin negative OrphaNet|HPO C0015230 Exanthem C0343060 Pityriasis; rotunda UMLS C0041834 Erythematous condition C0263627 Calcinosis universalis OrphaNet|HPO C0406671 Burning scrotum C0406669 Psychogenic sensory disturbance of skin UMLS C0013404 Respiratory difficulty C1961100 Erectile dysfunction adverse event HSDN C0917816 Deficiency mental C2678263 Methylmalonic acidemia, cblh type, formerly HPO C1963087 Constipation adverse event C0039006 Swine--diseases HSDN C4085642 Level of joint stiffness C0265287 Acromicric dysplasia MalaCards|HPO C0004093 Asthenia C0006107 Concussion HSDN C0042963 Symptoms vomiting C0003618 Appetites HSDN C3146279 Coma C0042487 Venous thrombosis HSDN C0040264 Ear ringing sound C0001175 Acquired immunodeficiency syndrome HSDN C3665347 Vision impaired C1112155 Hereditary non-polyposis colorectal cancer syndrome HPO C0027497 Queasy C0079774 Peripheral t-cell lymphoma HSDN C0010520 Skin cyanosis C0016542 Foreign body HSDN C2032395 Pelvic pain on the left C1962963 Osteoporosis adverse event HSDN C0016199 Pain flank C0027656 Neoplasms, connective tissue HSDN C0040822 D tremors C1837713 Joubert syndrome 3 MalaCards C0018784 Deafness sensorineural C0796062 Microcephaly-deafness syndrome OrphaNet|MalaCards C0747556 Pharyngitis recurrent C0085253 Adult-onset still disease MalaCards C1384666 Decreased hearing C1849334 Robinow syndrome, autosomal recessive OrphaNet|HPO|MalaCards C4085211 Pain distress question C0027644 Neoplasm regression, spontaneous HSDN C0014724 Burping C0038644 Sudden infant death syndrome HSDN C4084773 Bothered by weight gain C0021841 Intestinal neoplasms HSDN C2911645 Weight loss adverse event C0020456 Hyperglycemia HSDN C0020672 Body temperature decreased C0039128 Syphilis HSDN C0013604 Edematous C0020473 Hyperlipidemia HSDN C0221263 Cafe au lait spot C0265673 Congenital kyphosis HSDN C1963091 Diarrhea adverse event C0021843 Intestinal obstruction HSDN C1549543 Administration method - pain C0017075 Ganglioneuroma HSDN C2984057 Have nausea C0344315 Depressed mood HSDN C2203646 Jaundice C0334489 Pancreatoblastoma MalaCards C0039070 Collapse fleeting C0037650 Somatoform disorder HSDN C4084768 Usual severity vomiting C0037116 Silicosis HSDN C4084767 Bothered by vomiting C0016542 Foreign body HSDN C0015970 Fever unknown origin C0004364 Autoimmune diseases HSDN C0012833 Dizzy C0034186 Pyelonephritis HSDN C0017565 Gingiva hemorrhage C0015519 Factor x deficiency MalaCards C3641755 Have constipation C0020255 Hydrocephalus HSDN C0000731 Abdomen distention C0085090 Lymphoma, aids-related MalaCards C1963091 Diarrhea adverse event C0034089 Pulmonary valve stenosis HSDN C3665347 Vision impaired C1857821 Leber congenital amaurosis 10 (disorder) MalaCards|HPO C1963065 Apnea adverse event C0023890 Liver cirrhosis HSDN C0016382 Cutaneous vascular engorgement C1849193 Peeling skin syndrome MalaCards|HPO C1962972 Proteinuria adverse event C0242528 Azotemia HSDN C2024893 Cardiovascular surgery result: fatigue C1366535 Avp gene HSDN C0013911 Emaciate C0034013 Precocious puberty HSDN C0576456 Poor feeding C1970482 Potocki-lupski syndrome MalaCards C0723402 Sore throat C0042470 Guanarito haemorrhagic fever MalaCards C0424755 Fever symptoms C0029291 Fever, parrot DiseaseOntology|HSDN|MalaCards C0018681 Headache, cephalalgia C1332190 Adult brain oligodendroglioma UMLS C0242936 Center pain C0042253 Vaginal fistula HSDN C1838869 Proximal neurogenic muscle weakness C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards|HPO C0026858 Musculoskeletal pain C0001721 Emotional affect HSDN C0577569 Mass of male genital structure C0496891 Benign neoplasm of male genital organ UMLS C4084773 Bothered by weight gain C0035228 Respiratory hypersensitivity HSDN C0557874 Global developmental delay C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C3829611 Nausea frequency C0013922 Embolism HSDN C0011991 Loose stools C0010414 Infection by cryptococcus neoformans HSDN C3274924 Have been coughing C2706915 Language:-:point in time:^patient:- HSDN C0473129 Diarrhea after git surgery C1285297 Gastrointestinal complication of procedure UMLS C4084766 Vomiting C0494039 Gastrointestinal tularaemia MalaCards C0085602 Polydypsia C1847013 Nephronophthisis 4 MalaCards|HPO|UMLS C0042963 Symptoms vomiting C0009187 Coccidiosis HSDN C0037384 Snore C1962979 Burn adverse event HSDN C4084788 Have dizziness C0035243 Respiratory tract infections HSDN C0460137 Push down or depress C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C2984058 Have pain C0029412 Hypertrophic pulmonary osteoarthropathy HSDN C0031911 Pigment deposition C0346782 Malignant melanoma of scalp and neck nos MalaCards C0004134 Dyssynergia C0025294 Meningococcal meningitis HSDN C0085631 Abnormal excitement C1843792 Frontotemporal lobar degeneration with tdp43 inclusions, grn-related HPO|UMLS C0241165 Skin thickening C1850079 Parana hard skin syndrome OrphaNet|MalaCards C4084775 Usual severity weight loss C0042076 Urologic neoplasms HSDN C0575081 Abnormal gait C1856051 Daish hardman lamont syndrome MalaCards C0042798 Vision dim C0025284 Meningeal neoplasms HSDN C3898969 Have been vomiting C1999266 Depression adverse event HSDN C3641756 Have diarrhea C0342288 Insulin-dependent diabetes mellitus secretory diarrhea syndrome MalaCards|HPO C0349588 Stature short C0271561 Somatotropin deficiency OrphaNet|MalaCards C4084766 Vomiting C0025297 Viral meningitis HSDN C4085211 Pain distress question C0030271 Pancoast syndrome HSDN C0030552 Paralysis partial C1855606 Burton syndrome MalaCards C2237041 Shox gene with short stature C1855081 Microcephaly, primary autosomal recessive, 1 MalaCards|HPO C4084725 Usual severity cough C1552262 Nurse practitioner - family HSDN C0009676 Confusion state C0019693 Hiv infections HSDN C0221752 Rbc urine C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C0026838 Spasticity muscle C0751666 Canavan disease, infantile OrphaNet|HPO C0020578 Hyperventilate C0041327 Tuberculosis, pulmonary HSDN C3887638 Failure to thrive in infant C3711125 Mitochondrial dna depletion syndrome 8a MalaCards C0027497 Queasy C0009241 Cognition disorders HSDN C0221166 Paraparesis C0018923 Hemangiosarcoma HSDN C1963281 Vomiting adverse event C0037036 Sialorrhea HSDN C0518090 Frequency of pain question C0031039 Effusion pericardial HSDN C0085593 Chill C0036231 Sarcocystosis DiseaseOntology C0518090 Frequency of pain question C0002170 Alopecia HSDN C0009421 Comatose C0015745 Ingestive behavior HSDN C0030193 Sense of pain C0311468 Increased bilirubin level (finding) HSDN C0019080 Bleed_nos problem C3468041 Fanconi anemia, complementation group c MalaCards C3539895 Pelvic pain occurs with bowel movement C0019693 Hiv infections HSDN C0030486 Extremity paralysis, lower C2117118 X-ray of toe: deformity contracture HSDN C4085548 Usual severity dizziness C0023055 Laryngeal neoplasm HSDN C3146279 Coma C0019294 Hernia, inguinal HSDN C0006370 Bulimia C0021655 Insulin resistance HSDN C1549543 Administration method - pain C0035923 German measles vaccine HSDN C2984057 Have nausea C0041466 Typhoid fever HSDN C0031911 Pigment deposition C0153529 Malignant melanoma of lip MalaCards C3815497 Cough C0012644 Animal disease models HSDN C1963249 Tinnitus adverse event C0024141 Lupus erythematosus, systemic HSDN C0018681 Headache, cephalalgia C0007194 Hypertrophic cardiomyopathy HSDN C1963184 Nystagmus adverse event C1864100 Pseudohypoparathyroidism, type ib OrphaNet|HPO|MalaCards C0018834 Brash C1843042 Craniolenticulosutural dysplasia MalaCards|HPO C0030193 Sense of pain C0162679 Leukemic infiltration HSDN C3463815 Feel fatigue C0023827 Liposarcoma MalaCards C0233514 Behavior abnormal C0041341 Tuberous sclerosis OrphaNet|HPO C3887638 Failure to thrive in infant C0342474 Lipoid congenital adrenal hyperplasia OrphaNet C0917816 Deficiency mental C0175683 Citrullinemia HPO C4084802 Usual severity diarrhea C0004161 Athletic injuries HSDN C3898969 Have been vomiting C0035435 Rheumatism HSDN C0270790 Quadriparesis C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards|UMLS C4084784 Diarrhea C0013720 Ehlers-danlos syndrome HSDN C0349588 Stature short C1832817 Klippel-feil deformity, conductive deafness, and absent vagina OrphaNet|MalaCards C0013456 Pain ear C0033036 Atrial premature complexes HSDN C1963071 Back pain adverse event C1704421 Skin pigmentation disorder HSDN C4084767 Bothered by vomiting C0034494 Rabies (disorder) HSDN C0018681 Headache, cephalalgia C0029463 Osteosarcoma HSDN C0231528 Muscle pain generalized C1956390 Cranial arteritis MalaCards C3163620 Hypotension adverse event C2242987 Benign mastocytoma MalaCards C0011991 Loose stools C0039336 Gustatory sense HSDN C3463815 Feel fatigue C0042510 Ventricular fibrillation HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0035243 Respiratory tract infections HSDN C0242936 Center pain C0027726 Nephrotic syndrome HSDN C0000737 Abdomen pain C0016879 Fusobacterium infections HSDN C0020455 Hypergammaglobulinemia C0024305 Lymphoma, non-hodgkin HSDN C0011991 Loose stools C0276478 Coronaviral calf diarrhea UMLS C4084775 Usual severity weight loss C0025063 Mediastinal neoplasms HSDN C2919142 Short stature adverse event C1858723 Poikiloderma with neutropenia MalaCards|HPO C2919142 Short stature adverse event C2749477 Oculodentodigital dysplasia, autosomal recessive MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0004161 Athletic injuries HSDN C0086437 Joint hypermobility C1850674 Minicore myopathy with external ophthalmoplegia (disorder) MalaCards|HPO C4084775 Usual severity weight loss C0007125 Carcinoma, ehrlich tumor HSDN C0917816 Deficiency mental C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards C0026821 Cramp C0262655 Recurrent urinary tract infection HSDN C4085210 Usual severity pain C0012739 Disseminated intravascular coagulation HSDN C3898969 Have been vomiting C0342443 Adrenal cushing's syndrome HSDN C1962972 Proteinuria adverse event C3806275 Deafness and myopia MalaCards C0019209 Large liver C0036161 Sandhoff disease OrphaNet C0018772 Deafness C0016470 Food allergy HSDN C1959630 Eye pain adverse event C0752155 Central nervous system vascular malformations HSDN C2024893 Cardiovascular surgery result: fatigue C0022744 Knee injury HSDN C1963071 Back pain adverse event C0031117 Peripheral neuropathy HSDN C0427055 Face weakness C0027809 Neurilemmoma OrphaNet|MalaCards C0013456 Pain ear C0027073 Myofascial pain syndromes HSDN C0233514 Behavior abnormal C1844680 Deafness-hypogonadism syndrome OrphaNet|MalaCards C0007758 Cerebellar ataxia C0019693 Hiv infections HSDN C4085210 Usual severity pain C0546952 Congenital facial asymmetry HSDN C3829611 Nausea frequency C0039614 Tetanus HSDN C0026838 Spasticity muscle C1849722 Polyglucosan body disease, adult form OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0023290 Leishmaniasis, visceral HSDN C0011991 Loose stools C0149514 Bronchitis acute HSDN C4084769 Vomiting frequency C0024667 Animal mammary neoplasms HSDN C2029884 Hearing loss by exam C0026705 Mucopolysaccharidosis ii HSDN C0008031 Pain chest C0033578 Prostatic neoplasms HSDN C4084768 Usual severity vomiting C0005586 Bipolar disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035801 Diseases rodent HSDN C2029884 Hearing loss by exam C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0013144 Drowsy C1276035 Pena-shokeir syndrome type i OrphaNet C0151786 Weakness muscle C0040715 Chromosomal translocation HSDN C1963184 Nystagmus adverse event C1842836 Congenital disorder of glycosylation, type ii OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0032708 Disorders of porphyrin metabolism HSDN C0030232 Color loss C0024537 Malaria, vivax HSDN C0005874 Blush C3150986 Epileptic encephalopathy, early infantile, 7 MalaCards C4085210 Usual severity pain C4084971 Trachoma HSDN C2096293 Ent surgical result ear vertigo C0152264 Familial erythrocytosis OrphaNet|HPO C4084788 Have dizziness C0403447 Chronic kidney insufficiency HSDN C1962972 Proteinuria adverse event C0950122 Frasier syndrome MalaCards C1963281 Vomiting adverse event C0005974 Bone resorption HSDN C0027497 Queasy C0302148 Blood clot HSDN C0024031 Back pain lower back C0034734 Raynaud disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0009375 Colonic neoplasms HSDN C4084775 Usual severity weight loss C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C4084773 Bothered by weight gain C0014118 Endocarditis HSDN C1963071 Back pain adverse event C1334698 Meningothelial cell neoplasm MalaCards C2984057 Have nausea C0011119 Decompression sickness HSDN C0009676 Confusion state C0032914 Pre-eclampsia HSDN C3665386 Abnormal vision C2931673 Ceroid lipofuscinosis, neuronal 1, infantile OrphaNet|MalaCards C4084775 Usual severity weight loss C0013504 Echinococcosis, hepatic HSDN C4085211 Pain distress question C0016995 Gambling HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0205969 Thymic carcinoma OrphaNet|MalaCards C2919142 Short stature adverse event C3891449 Peeling skin syndrome 1 MalaCards C0751837 Gait ataxic C1332903 Cerebellar vermis medulloblastoma UMLS C2919142 Short stature adverse event C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards|HPO C0026838 Spasticity muscle C0008924 Cleft lip HSDN C0030193 Sense of pain C0008309 Bile duct adenoma HSDN C0012833 Dizzy C0039494 Temporomandibular joint disorders HSDN C0030193 Sense of pain C0002957 Anger HSDN C0151786 Weakness muscle C0038538 Effusion subdural HSDN C4084766 Vomiting C0007001 Carbohydrate metabolism, inborn errors HSDN C0004134 Dyssynergia C0024121 Lung neoplasms HSDN C0030193 Sense of pain C0020635 Hypopituitarism HSDN C0522224 Palsied C0007786 Brain ischemia HSDN C1579931 Depressed - symptom C0038868 Progressive supranuclear palsy OrphaNet C4084775 Usual severity weight loss C0152018 Esophageal carcinoma OrphaNet|MalaCards C2919142 Short stature adverse event C1840334 Hypoparathyroidism, autosomal recessive MalaCards C4042891 Sleep wake disorders C0034186 Pyelonephritis HSDN C2242996 Tingling C1836544 Schindler disease, type i MalaCards|HPO C0812426 Kidney problem C0554309 Prerenal uremia syndrome UMLS C0518090 Frequency of pain question C0016171 Fistula of intestine, excluding rectum and anus HSDN C3887873 Hearing loss C0006736 Body stone HSDN C0270948 Neurogenic muscular atrophy C0343108 Flynn aird syndrome OrphaNet|MalaCards C0020455 Hypergammaglobulinemia C1548483 Leishmaniasis vaccine HSDN C0040460 Dental pain C1579931 Depressed - symptom HSDN C4084727 Cough frequency C0028242 Nocardia infections HSDN C4084725 Usual severity cough C0009404 Colorectal neoplasms HSDN C0013404 Respiratory difficulty C2981277 Stage ivb thyroid gland undifferentiated (anaplastic) carcinoma UMLS C0518090 Frequency of pain question C0017563 Gingival diseases HSDN C4085661 Usual severity nausea C0017160 Gastroenteritis DiseaseOntology|HSDN C0282005 Scrotum swelling C0085605 Liver failure UMLS C3146279 Coma C0034069 Pulmonary fibrosis HSDN C0030193 Sense of pain C0004099 Asthma, exercise-induced HSDN C0232462 Appetite decrease C0037661 Somatostatinoma OrphaNet|MalaCards C0727671 Red cross toothache drops C0024121 Lung neoplasms HSDN C3898969 Have been vomiting C0005937 Bone cysts HSDN C0042571 Vertigo subjective C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) OrphaNet|HPO|MalaCards C0454644 Delayed language development C0265498 48, xxxy syndrome MalaCards C2919142 Short stature adverse event C3492944 Lentiginosis profusa MalaCards C0917816 Deficiency mental C1866850 Familial spastic paraplegia, mental retardation, and precocious puberty MalaCards C0575081 Abnormal gait C0265252 Coffin-lowry syndrome OrphaNet|HPO|MalaCards C3887873 Hearing loss C3888081 L-2-hydroxyglutaric acidemia MalaCards C3887638 Failure to thrive in infant C1868684 Ear, patella, short stature syndrome MalaCards|HPO C2984058 Have pain C0042376 Vascular headaches HSDN C0026838 Spasticity muscle C0282577 Congenital disorders of glycosylation MalaCards C0002962 Angina C1565489 Renal insufficiency HSDN C0424755 Fever symptoms C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0026826 High muscle tone C0795822 8 rec syndrome MalaCards C0858627 Intrapleural fluid retention of C0032227 Pleural effusion disorder UMLS C1557397 Adverse event associated with pain C0002950 Aneurysms inflammatory HSDN C3814530 Skin vesicle C0085652 Pyoderma gangrenosum MalaCards C1000483 Genus anemia C2931002 Congenital disorder of glycosylation type 1h MalaCards C1384666 Decreased hearing C2713321 Alpha-l-iduronidase deficiency OrphaNet C0033774 Skin pruritus C0036502 Sebaceous gland diseases HSDN C4084723 Constipation C0004935 Animal ethology HSDN C0018681 Headache, cephalalgia C0003860 Arteritis HSDN C0042571 Vertigo subjective C2364172 Adherence to medication regime HSDN C0011991 Loose stools C0267438 Dietetic diarrhea UMLS C2237041 Shox gene with short stature C2931604 Ring 6, chromosome OrphaNet|MalaCards C0522224 Palsied C1956346 Coronary artery disease HSDN C4085661 Usual severity nausea C0023448 Lymphoid leukemia HSDN C0042963 Symptoms vomiting C4012395 Congenital disorder of glycosylation, type iy MalaCards C0917816 Deficiency mental C3151187 Seckel syndrome 5 MalaCards C0018777 Deafness, conductive C0016037 Fibrodysplasia ossificans progressiva MalaCards|HPO C3887638 Failure to thrive in infant C0020598 Hypocalcemia HSDN C0728710 Pupil constriction observed C1458155 Mammary neoplasms HSDN C0036572 Convulsion C0268281 Infantile neuronal ceroid lipofuscinosis OrphaNet|HPO|MalaCards C3887873 Hearing loss C0004933 Behavior modification technique HSDN C1963065 Apnea adverse event C0220981 Metabolic acidosis HSDN C3829611 Nausea frequency C2945560 Hemolytic HSDN C0270844 Convulsions tonic C2168320 Lennox-gastant syndrome with tonic seizures UMLS C2237041 Shox gene with short stature C0265756 Congenital atresia of larynx OrphaNet|MalaCards C0020615 Hypoglycemia nos C0268569 Intermittent maple syrup urine disease HPO C3146279 Coma C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal OrphaNet|HPO C3898969 Have been vomiting C0013274 Patent ductus arteriosus HSDN C0013404 Respiratory difficulty C0038436 Post-traumatic stress disorder HSDN C0020450 Hyperemesis gravidarum C0020451 Mild hyperemesis gravid. nos UMLS C0020903 Illusion C0042795 Entoptic phenomena HSDN C4085210 Usual severity pain C2117329 X-ray of toe: polydactyly HSDN C4084725 Usual severity cough C1261473 Sarcoma HSDN C0233844 Awkwardness C2751842 Parkinson disease 14, autosomal recessive MalaCards|HPO|UMLS C3641755 Have constipation C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO C4084768 Usual severity vomiting C0015814 Femur head necrosis HSDN C0030193 Sense of pain C0024314 Lymphoproliferative disorders HSDN C0000727 Abdomen acute C0021833 Intestinal fistula HSDN C3887873 Hearing loss C0041374 Tumor virus infections HSDN C0026821 Cramp C0160680 Carotid artery injury HSDN C0151686 Growth retardation C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C3641756 Have diarrhea C0010481 Cushing syndrome HSDN C0003862 Pain joint C0162565 Acute intermittent porphyria MalaCards|HPO C0857066 Catarrhal lumps C0027441 Nasopharyngitis UMLS C2919142 Short stature adverse event C1864825 Frias syndrome MalaCards C0018772 Deafness C0035229 Respiratory insufficiency HSDN C3496180 Sleep apnea C1842025 Glaucoma and sleep apnea OrphaNet|MalaCards C0011991 Loose stools C1855869 Autoimmune polyendocrinopathy syndrome, type i, autosomal dominant HPO C0917816 Deficiency mental C1851100 Laurin-sandrow syndrome MalaCards|HPO C1069915 Vertigo C0015464 Facial nerve diseases HSDN C0013911 Emaciate C0041325 Peritonitis, tuberculous MalaCards C4084767 Bothered by vomiting C0035305 Retinal detachment HSDN C0013404 Respiratory difficulty C0549143 Pulmonary renal syndrome MalaCards C0860603 Anxiety symptom C0268275 Tay-sachs disease, ab variant MalaCards C4084776 Weight loss C0042164 Uveitis HSDN C0003811 Cardiac rhythm disturbance C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C1963252 Tremor adverse event C0270726 Alexander disease OrphaNet|HSDN|MalaCards C1963086 Confusion adverse event C0020538 Hypertensive disease HSDN C4085210 Usual severity pain C1138434 Disease, x-linked genetic HSDN C0006370 Bulimia C2350521 Gustatory perception HSDN C0018772 Deafness C0022665 Kidney neoplasm HSDN C4085317 Diarrhea frequency C0014175 Endometriosis HSDN C3146279 Coma C0003460 Anurias HSDN C2984058 Have pain C1009209 Tinea HSDN C4085317 Diarrhea frequency C0848377 Trauma to the abdomen HSDN C0152459 Striae C2697932 Loeys-dietz syndrome OrphaNet|HPO|MalaCards C0427068 Legs weakness C3150901 Spastic paraplegia 48, autosomal recessive MalaCards|HPO C0042928 Paralysis vocal cord C0039130 Cardiovascular syphilis HSDN C0013911 Emaciate C0238096 Embolism, paradoxical HSDN C3463815 Feel fatigue C0028432 Nose diseases HSDN C0231528 Muscle pain generalized C0011644 Scleroderma OrphaNet|MalaCards C0085642 Asphyxia reticularis C0040021 Thromboangiitis obliterans HSDN C1549543 Administration method - pain C0022680 Polycystic kidney diseases HSDN C4085862 Bothered by nausea C0085096 Peripheral vascular diseases HSDN C0349588 Stature short C0796016 Microphthalmia, syndromic 1 OrphaNet|HPO|MalaCards C0013405 Dyspnea, paroxysmal C0018809 Heart neoplasm HSDN C0010520 Skin cyanosis C0453996 Tobacco smoking HSDN C1557397 Adverse event associated with pain C0238461 Anaplastic thyroid carcinoma OrphaNet C0860603 Anxiety symptom C1849157 Insulin-like growth factor i, resistance to MalaCards|HPO C1557397 Adverse event associated with pain C0282488 Interstitial cystitis OrphaNet|MalaCards C4084774 Have weight loss C0038358 Gastric ulcer HSDN C0018772 Deafness C1552262 Nurse practitioner - family HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042514 Tachycardia, ventricular HSDN C3463815 Feel fatigue C0030767 Grouping peer HSDN C3641756 Have diarrhea C1546558 Specimen source codes - blister HSDN C2984058 Have pain C0010414 Infection by cryptococcus neoformans HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C0018772 Deafness C0265234 Branchio-oto-renal syndrome OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0026764 Multiple myeloma HSDN C4084724 Usual severity constipation C0220998 Hypothalamic hypothyroidism MalaCards C4084774 Have weight loss C0013502 Echinococcosis HSDN C4085317 Diarrhea frequency C1384665 Hfe gene HSDN C0235198 Disturbed mental concentration C0022340 Late-infantile neuronal ceroid lipfuscinosis MalaCards C0003862 Pain joint C3244301 Coverage level - family HSDN C2315100 Pediatric failure to thrive C0268574 Hyperleucine-isoleucinemia MalaCards C4084784 Diarrhea C0020875 Ileal diseases HSDN C4042891 Sleep wake disorders C0012746 Dissociative disorder HSDN C0019079 Bloody sputum C0037998 Splenic infarction HSDN C4085211 Pain distress question C1691228 Cystic kidney diseases HSDN C2203646 Jaundice C0037355 Smallpox vaccines HSDN C2984057 Have nausea C1963064 Anxiety adverse event HSDN C0242670 Chronic vegetative state C0007784 Cerebral hemisphere hemorrhage HSDN C2215257 Acute postoperative pain C1719390 Acute post-thoracotomy pain UMLS C1860844 Sparse, thin hair C0392475 Roberts-sc phocomelia syndrome OrphaNet|HPO|MalaCards C0040264 Ear ringing sound C0003708 Arachnitis OrphaNet|MalaCards C2911645 Weight loss adverse event C1868502 Pemphigus vulgaris, familial MalaCards C4085210 Usual severity pain C0022650 Kidney calculi HSDN C0040822 D tremors C1963198 Pancreatitis adverse event HSDN C0000737 Abdomen pain C2217038 Stage iiib colon cancer UMLS C0023014 Developmental disorder language C0025958 Microcephaly HSDN C0018681 Headache, cephalalgia C0348018 Projections HSDN C4085210 Usual severity pain C0005398 Cholestasis, extrahepatic HSDN C4084773 Bothered by weight gain C0582587 Visual learning HSDN C0497247 Blood pressure elevation C0032001 Pituitary apoplexy OrphaNet|MalaCards C3887638 Failure to thrive in infant C2700431 Mitochondrial complex v (atp synthase) deficiency, atpaf2 type HPO C0033774 Skin pruritus C2987165 Pancreatic hepatoid adenocarcinoma UMLS C0557874 Global developmental delay C0023264 Leigh disease MalaCards|HPO C0018784 Deafness sensorineural C0520679 Sleep apnea, obstructive HSDN C0027796 Neuralgias C0003850 Arteriosclerosis HSDN C0040264 Ear ringing sound C0004096 Asthma HSDN C4084727 Cough frequency C0042487 Venous thrombosis HSDN C0020455 Hypergammaglobulinemia C0040034 Thrombocytopenia HSDN C0231528 Muscle pain generalized C0206138 Crest syndrome MalaCards C1549543 Administration method - pain C0036039 Sadism HSDN C3665347 Vision impaired C0001144 Acne vulgaris MalaCards C1549543 Administration method - pain C0010414 Infection by cryptococcus neoformans HSDN C0030200 Intractable pain C0033873 Psychiatry HSDN C0009806 Constipate C0085576 Iron-refractory iron deficiency anemia UMLS C0026838 Spasticity muscle C0023890 Liver cirrhosis HSDN C0424755 Fever symptoms C0019151 Hepatic encephalopathy HSDN C1963252 Tremor adverse event C3554398 Spinal muscular atrophy, jokela type MalaCards C0242936 Center pain C0030977 Perceptual masking HSDN C1000483 Genus anemia C1858990 Beta thalassemia, dominant inclusion body type OrphaNet C3665492 Pigmentations C0751383 Juvenile neuronal ceroid lipofuscinosis MalaCards C4084766 Vomiting C0035220 Respiratory distress syndrome, newborn HSDN C4085211 Pain distress question C0006267 Bronchiectasis HSDN C3641756 Have diarrhea C0032269 Pneumococcal infections HSDN C0009806 Constipate C0018939 Hematological disease HSDN C1557397 Adverse event associated with pain C0033700 Infection proteus HSDN C0240715 Perineal lump C0037859 Spermatocele UMLS C0022346 Yellow skin C3151421 Cyanosis, transient neonatal MalaCards|HPO C4084802 Usual severity diarrhea C0342443 Adrenal cushing's syndrome HSDN C0011991 Loose stools C2073625 X-ray of chest: pleural effusion HSDN C4084776 Weight loss C0007130 Mucinous adenocarcinoma HSDN C3815497 Cough C3203727 Pneumorrhachi HSDN C0011991 Loose stools C1456781 Benign melanocytic nevus HSDN C4084726 Distress cough C2004491 Cicatrix HSDN C0476273 Distress respiratory C2931888 Pfeiffer type acrocephalosyndactyly MalaCards C0575081 Abnormal gait C2750785 Muscular dystrophy, congenital, lmna-related (disorder) OrphaNet|HPO C4084775 Usual severity weight loss C0033805 Pseudohypoaldosteronism HSDN C2919142 Short stature adverse event C0265756 Congenital atresia of larynx OrphaNet|MalaCards C0034933 Abnormal reflexes C0020255 Hydrocephalus HSDN C0426579 Anorexia symptom C0376618 Endotoxemia HSDN C0018772 Deafness C0013446 Acquired ear deformities HSDN C0012833 Dizzy C0003811 Cardiac arrhythmia HSDN C0162298 Stiffness joints C0220668 Congenital contractural arachnodactyly OrphaNet|HPO C3898969 Have been vomiting C0085389 Bacillaceae infection HSDN C0002170 Alopecia disorders C0026755 Multiple carboxylase deficiency OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C2931785 Juvenile dermatomyositis MalaCards C0700078 Deep tendon reflex decrease C1834846 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 HPO C2984058 Have pain C0161406 Injury nerve trigeminal HSDN C1549543 Administration method - pain C0033968 Psychotherapeutic technique HSDN C0003469 Anxiety disorder C2678416 Hyperphenylalaninemia, non-pku mild HPO C3829611 Nausea frequency C0022410 Joint instability HSDN C1963091 Diarrhea adverse event C1548777 Specimen reject reason - hemolysis HSDN C0043094 Weight gain C0026640 Mouth neoplasms HSDN C0011991 Loose stools C0032087 Plant poisoning HSDN C0018681 Headache, cephalalgia C0016053 Fibromyalgia HSDN C2096293 Ent surgical result ear vertigo C1334410 Localized primitive neuroectodermal tumor MalaCards C0577560 Eye mass C0339136 Cyst; lacrimal apparatus UMLS C0013390 Cramps menstrual C2586211 Thrombosis of blood vessel HSDN C0015970 Fever unknown origin C0030499 Parasitic diseases HSDN C0026826 High muscle tone C0027765 Nervous system disorder HSDN C0019209 Large liver C1868679 Griscelli syndrome, type 2 OrphaNet|HPO|MalaCards C0000727 Abdomen acute C0004238 Atrial fibrillation HSDN C4085210 Usual severity pain C0018965 Hematuria HSDN C0013132 Drooling C1412397 Ancr gene HPO C0009806 Constipate C0026850 Muscular dystrophy HSDN C2919142 Short stature adverse event C1970109 Aromatase excess syndrome MalaCards C0013595 Eczematous dermatitis C0263311 Senile dermatitis herpetiform MalaCards C1279888 Proteinuria of undiagnosed cause C2931125 Feigenbaum bergeron richardson syndrome OrphaNet|MalaCards C4084788 Have dizziness C1546533 Specimen source codes - abscess HSDN C0020672 Body temperature decreased C0597109 Nurse's role HSDN C1557397 Adverse event associated with pain C1522057 Acute enteritis of the mouse intestinal tract HSDN C4084727 Cough frequency C0149514 Bronchitis acute MalaCards C0018965 Blood urine C1851986 Dyschondrosteosis and nephritis OrphaNet|MalaCards C0030794 Pelvis pain C0041311 Tuberculosis, female genital HSDN C0878773 Bladder hyperactive C0037369 Smoking HSDN C0030200 Intractable pain C0042830 Perception visual HSDN C0013604 Edematous C0018023 Nodular goiter HSDN C4084723 Constipation C0042029 Urinary tract infection HSDN C0035232 Diaphragmatic paralysis C0398562 Triose phosphate isomerase deficiency OrphaNet|HPO C0040822 D tremors C1706920 Benign pheochromocytoma of adrenal gland UMLS C2984058 Have pain C0037023 Sialadenitis HSDN C0850758 Pain pelvic C1962979 Burn adverse event HSDN C0497406 Over weight C0026769 Multiple sclerosis HSDN C2315100 Pediatric failure to thrive C0035934 Rubinstein-taybi syndrome MalaCards|HSDN|HPO C0349489 Fetal hypoxia C0002891 Anemia, neonatal HSDN C0243026 Generalized infection C0021100 Bullous impetigo MalaCards C0750426 Wbc elevated C0343068 Familial cold urticaria HPO C1963184 Nystagmus adverse event C2749345 Refsum disease, adult, 1 HPO C0020505 Excessive eating C1610547 Production class code - pleasure HSDN C0042024 Urine incontinence C0021364 Male infertility HSDN C0851578 Disorder sleep C0006663 Calcinosis HSDN C0030193 Sense of pain C0030482 Paraepithymia HSDN C4084766 Vomiting C0004943 Behcet syndrome HSDN C0042571 Vertigo subjective C1963229 Retinal detachment adverse event HSDN C0518090 Frequency of pain question C0006705 Calcium metabolism disorders HSDN C0018772 Deafness C3714756 Intellectual disability MalaCards C4084725 Usual severity cough C0023343 Leprosy HSDN C0003862 Pain joint C0460136 Barotrauma HSDN C1971624 Appetite absent C2219717 Menstrual periods stopped for over 6 months HSDN C0018681 Headache, cephalalgia C3813607 Infantile gastroesophageal reflux HSDN C0020538 Hbp C0270726 Alexander disease MalaCards C0030486 Extremity paralysis, lower C0019372 Herpesviridae infections HSDN C0009806 Constipate C0005695 Bladder neoplasm HSDN C0151889 Reflexes tendon increased C1845243 Mental retardation, x-linked, syndromic, claes-jensen type OrphaNet|HPO|MalaCards C0042384 Vasculitis, nonspecific C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0030193 Sense of pain C0269118 Endometriosis bladder UMLS C0264599 Aphonia paralytica C0264309 Cord disorders vocal UMLS C2585575 Recurrent abdominal pains C1275126 Tnf receptor-associated periodic fever syndrome (traps) UMLS C3463815 Feel fatigue C0027145 Myxedema MalaCards C1963087 Constipation adverse event C0344434 Atrial fibrillation ecg HSDN C0042024 Urine incontinence C0026848 Myopathy HSDN C2242996 Tingling C0022972 Lambert-eaton myasthenic syndrome HSDN C1557397 Adverse event associated with pain C0085632 Apathy HSDN C1963087 Constipation adverse event C0016658 Fracture bone HSDN C4084767 Bothered by vomiting C0013870 Electroconvulsive shock HSDN C0031315 Phantom limb pain C0026650 Movement disorders HSDN C0018775 Hearing loss bilateral C0037369 Smoking HSDN C0242936 Center pain C0006107 Concussion HSDN C0002962 Angina C0403447 Chronic kidney insufficiency HSDN C1963087 Constipation adverse event C0032285 Pneumonia HSDN C2315100 Pediatric failure to thrive C1869122 Ehlers-danlos syndrome, progeroid form HPO C1549543 Administration method - pain C0302182 Trabecular adenocarcinoma MalaCards C0086565 Liver function abnormal C0019101 Hemorrhagic fever with renal syndrome OrphaNet|MalaCards C2237041 Shox gene with short stature C1860991 Noonan syndrome 3 MalaCards|HPO C2911645 Weight loss adverse event C0028960 Oligospermia HSDN C0413252 Hypothermia due to exposure C0004623 Bacterial infections HSDN C0043094 Weight gain C0042029 Urinary tract infection HSDN C0018784 Deafness sensorineural C0265223 Cohen syndrome HPO C0013404 Respiratory difficulty C0006277 Bronchitis DiseaseOntology|MalaCards C0026838 Spasticity muscle C3698507 Porencephaly, post-traumatic MalaCards C4085862 Bothered by nausea C0162576 Anisakiasis MalaCards C0238637 Anus pain C0003462 Anus diseases UMLS C0008031 Pain chest C0878544 Cardiomyopathies UMLS C1963170 Hypothermia adverse event C0023364 Leptospirosis HSDN C0011991 Loose stools C0027540 Necrosis HSDN C4084802 Usual severity diarrhea C0032787 Postoperative complications HSDN C2029884 Hearing loss by exam C0035923 German measles vaccine HSDN C0040485 Wryneck C0453996 Tobacco smoking HSDN C0042024 Urine incontinence C1849322 Sandhoff disease, infantile type HPO C4084727 Cough frequency C0268250 Gaucher disease, type 2 (disorder) OrphaNet|HPO|MalaCards C0241210 Speaking delay C2675179 Arginine:glycine amidinotransferase deficiency MalaCards|HPO C0036572 Convulsion C3899662 Childhood fibrillary astrocytoma UMLS C0086439 Activity decreased C0752109 Brain diseases, metabolic, inborn HSDN C0000737 Abdomen pain C0016057 Fibrosarcoma HSDN C3463815 Feel fatigue C0019196 Hepatitis c DiseaseOntology|HSDN|MalaCards C0162298 Stiffness joints C0853804 Early morning joint stiffness UMLS C4084775 Usual severity weight loss C3714580 Hypokalemic periodic paralysis type 1 HSDN C4085211 Pain distress question C1136154 Dysfunction, tibialis posterior HSDN C4084726 Distress cough C0030286 Pancreatic diseases HSDN C4084776 Weight loss C0436596 On examination - apathetic HSDN C0080274 Retention urinary C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C4084776 Weight loss C0948089 Acute coronary syndrome HSDN C0427008 Stiffness C0018523 Hallervorden-spatz syndrome MalaCards|UMLS C0150055 Pain chronic C1860549 Uterus bicornis bicollis with partial vaginal septum and unilateral hematocolpos with ipsilateral renal agenesis MalaCards C1971624 Appetite absent C0002871 Anemia HSDN C0019825 Voice hoarseness C0206706 Verrucous carcinoma HSDN C2911645 Weight loss adverse event C0037397 Behavior social HSDN C0231528 Muscle pain generalized C1855606 Burton syndrome MalaCards C0023015 Language handicap C0024534 Malaria, cerebral HSDN C0042964 Anticipatory vomiting C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2132198 Abnormal blistering of the skin C0162566 Porphyria cutanea tarda OrphaNet|MalaCards C0030552 Paralysis partial C0019348 Herpes simplex infections HSDN C0242936 Center pain C0751396 Well differentiated oligodendroglioma HSDN C4084773 Bothered by weight gain C0162316 Iron deficiency anemia HSDN C0344232 Blurred vision C1865323 Migraine, familial basilar HPO C0027497 Queasy C0151740 Intracranial hypertension HSDN|UMLS C4084767 Bothered by vomiting C0020523 Immediate hypersensitivity HSDN C0727671 Red cross toothache drops C0152177 Trigeminal neuropathy HSDN C0034151 Hyperglobulinemic purpura C0750394 Wbc low HSDN C0013604 Edematous C0024137 Lupus erythematosus, cutaneous OrphaNet C0557874 Global developmental delay C1849508 Epilepsy, pyridoxine-dependent OrphaNet|HPO|MalaCards C4018871 Abnormality of the respiratory system C1843153 Charcot-marie-tooth disease, type 2j HPO C0007758 Cerebellar ataxia C1835614 Hereditary hyperexplexia MalaCards C0349588 Stature short C1838779 Eiken skeletal dysplasia OrphaNet|HPO|MalaCards C0030554 Abnormal sensation C0030297 Pancreatic neoplasm HSDN C0460137 Push down or depress C0002986 Fabry disease MalaCards|HPO C1963087 Constipation adverse event C0013182 Drug allergy HSDN C3274924 Have been coughing C0022116 Ischemia HSDN C0005779 Clotting C0024454 Maffucci syndrome MalaCards C0023015 Language handicap C0008065 Childhood behavior HSDN C0086437 Joint hypermobility C4014831 Vesicoureteral reflux 8 MalaCards C0575081 Abnormal gait C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C0042024 Urine incontinence C0042133 Uterine fibroids HSDN C2024893 Cardiovascular surgery result: fatigue C0238198 Gastrointestinal stromal tumors OrphaNet|HPO|MalaCards C0040264 Ear ringing sound C0556520 Psychological desensitization HSDN C1963252 Tremor adverse event C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C2911647 Weight gain adverse event C0311386 Isosporiasis HSDN C0018681 Headache, cephalalgia C0019151 Hepatic encephalopathy HSDN C0751265 Learning disability C2931119 Mehes syndrome MalaCards C4042891 Sleep wake disorders C0003477 Separation anxiety disorder HSDN C0015300 Ocular proptosis C0432367 Aminopterin embryopathy syndrome OrphaNet|MalaCards C0026838 Spasticity muscle C0393591 Aicardi-goutieres syndrome OrphaNet|HPO|MalaCards C1963184 Nystagmus adverse event C1838979 Mitochondrial complex i deficiency MalaCards|HPO C4084723 Constipation C0019080 Hemorrhage HSDN C2237041 Shox gene with short stature C0004135 Ataxia telangiectasia OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0919267 Ovarian neoplasm HSDN C2984057 Have nausea C0206696 Carcinoma, signet ring cell HSDN C3665492 Pigmentations C1333375 Ectopic thymus MalaCards C1260880 Nasal drip C1334645 Inverted papilloma of maxillary sinus UMLS C4085222 Nausea C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C0029163 Hemorrhage mouth C0017570 Gingival neoplasms HSDN C1963184 Nystagmus adverse event C1855255 Pseudoarylsulfatase a deficiency MalaCards C0151686 Growth retardation C0265219 Miller dieker syndrome OrphaNet|HPO|MalaCards C0026821 Cramp C0022660 Kidney failure, acute HSDN C1963184 Nystagmus adverse event C0796264 Young-hughes syndrome MalaCards C0033774 Skin pruritus C0023343 Leprosy HSDN C4085548 Usual severity dizziness C0023448 Lymphoid leukemia HSDN C0009421 Comatose C0020732 Iatrogenic disease HSDN C1963170 Hypothermia adverse event C0038454 Cerebrovascular accident HSDN C0037763 Spasm C0022661 Kidney failure, chronic HSDN C0015468 Face pain C0027809 Neurilemmoma HSDN C0030193 Sense of pain C0458224 Piriformis syndromes UMLS C0233514 Behavior abnormal C0796081 Growth mental deficiency syndrome of myhre MalaCards C0518090 Frequency of pain question C0236664 Alcohol-related disorders HSDN C1963137 Hydrocephalus adverse event C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C0004134 Dyssynergia C0496842 Malignant neoplasm of pituitary gland MalaCards C0034150 Skin purpura C1962986 Glaucoma adverse event HSDN C1279888 Proteinuria of undiagnosed cause C0032787 Postoperative complications HSDN C0042963 Symptoms vomiting C0001768 Agammaglobulinemia HSDN C4084727 Cough frequency C0022660 Kidney failure, acute HSDN C0033774 Skin pruritus C3826850 Vulvar intraepithelial neoplasia, usual type UMLS C0013362 Dysarthrias C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0151786 Weakness muscle C0011875 Diabetic angiopathies HSDN C0027066 Myoclonic jerking C0038273 Stereotypic movement disorder HSDN C0013911 Emaciate C0020550 Hyperthyroidism HSDN C0018834 Brash C1845530 Stocco dos santos syndrome MalaCards C0151827 Pain eye C1962958 Hematoma adverse event HSDN C0231528 Muscle pain generalized C0877265 Trichophyton infection MalaCards C1279888 Proteinuria of undiagnosed cause C2936917 Infantile polyarteritis MalaCards C0151786 Weakness muscle C3813553 Notch3 wt allele HSDN C0027796 Neuralgias C0563150 Catastrophization HSDN C0151686 Growth retardation C2675369 Chromosome 22q11.2 microduplication syndrome HPO C0000727 Abdomen acute C0264766 Rheumatic mitral stenosis HSDN C0030552 Paralysis partial C0006309 Brucellosis HSDN C2169806 Tic C0020936 Imitative behaviors HSDN C0427202 Atony, muscular C0267222 Ruminal atony UMLS C2984058 Have pain C0014742 Erythema multiforme HSDN C0034150 Skin purpura C0040046 Thrombophlebitis HSDN C4084766 Vomiting C0311375 Arsenic poisoning HSDN C0040822 D tremors C0019151 Hepatic encephalopathy HSDN C0027497 Queasy C0002895 Anemia, sickle cell HSDN C3887638 Failure to thrive in infant C2931294 Wiedemann grosse dibbern syndrome MalaCards C0392699 Dysaesthesia C0030554 Paresthesia UMLS C0024032 Birth weight subnormal C3809592 Mitochondrial dna depletion syndrome 13 (encephalomyopathic type) MalaCards C0020505 Excessive eating C0041296 Tuberculosis HSDN C0004134 Dyssynergia C1856973 Encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration MalaCards C1962972 Proteinuria adverse event C0026946 Mycoses HSDN C0019214 Hepatosplenomegaly C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards C0700072 Encounter due to stillbirth C0265267 Congenital hemidysplasia with ichthyosiform erythroderma and limb defects HPO C1963249 Tinnitus adverse event C0314657 Genetic predisposition HSDN C0042571 Vertigo subjective C0751815 Carotid artery, internal, dissection HSDN C0026826 High muscle tone C1834339 Myopathy, actin, congenital, with excess of thin myofilaments HPO C0003862 Pain joint C0021603 Sleep initiation and maintenance disorders HSDN C0019572 Hairiness C0033975 Psychotic disorders HSDN C0851578 Disorder sleep C0026850 Muscular dystrophy HSDN C0242936 Center pain C0030469 Paranasal sinus diseases HSDN C4084725 Usual severity cough C0005940 Bone diseases HSDN C0860603 Anxiety symptom C1849158 Insulin-like growth factor i, resistance to, due to increased binding protein HPO C4085211 Pain distress question C0027721 Lipoid nephrosis HSDN C3274924 Have been coughing C0085167 Granular cell tumor HSDN C0033774 Skin pruritus C0026848 Myopathy HSDN C0018989 Paresis of one side of body C0206245 Amyloid neuropathies, familial MalaCards C0011991 Loose stools C0031154 Peritonitis HSDN C0150055 Pain chronic C0011849 Diabetes mellitus HSDN C0042024 Urine incontinence C2748572 Sesame syndrome HPO C1384666 Decreased hearing C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C3898969 Have been vomiting C0042880 Vitamin k deficiency HSDN C0085128 Cardiac output elevated C0149721 Left ventricular hypertrophy HSDN C0015468 Face pain C0033923 Psychomotor function HSDN C0557874 Global developmental delay C3495588 Acrocephalopolydactylous dysplasia MalaCards C0264602 Spastic pseudobulbar dysphonia C0264600 Neurologic voice disorders UMLS C0027066 Myoclonic jerking C0039726 Disease, thalamic HSDN C0034933 Abnormal reflexes C0009375 Colonic neoplasms HSDN C2984058 Have pain C0009480 Community psychiatry HSDN C0003811 Cardiac rhythm disturbance C1866994 Ulnar-mammary syndrome MalaCards C0000737 Abdomen pain C0334533 Arteriovenous hemangioma HSDN C0557874 Global developmental delay C0795865 Chromosome 17, trisomy 17p OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0012813 Diverticulitis HSDN C0042571 Vertigo subjective C0155497 Active meniere's-cochlear UMLS C3641756 Have diarrhea C0024138 Lupus erythematosus, discoid HSDN C0033774 Skin pruritus C3489789 Cholestasis, progressive familial intrahepatic, 2 MalaCards|UMLS C3641756 Have diarrhea C0018099 Gout HSDN C0036572 Convulsion C0033677 Protein-energy malnutrition HSDN C4085317 Diarrhea frequency C0003467 Anxiety HSDN C4085317 Diarrhea frequency C3714580 Hypokalemic periodic paralysis type 1 HSDN C0019209 Large liver C3715199 Renal-hepatic-pancreatic dysplasia 1 MalaCards C0027497 Queasy C1963215 Pneumothorax adverse event HSDN C4085862 Bothered by nausea C1546635 Specimen source codes - fistula HSDN C4084784 Diarrhea C3661523 Congenital intestinal aganglionosis MalaCards|HPO C0349588 Stature short C3810023 Verheij syndrome MalaCards C3539895 Pelvic pain occurs with bowel movement C0023903 Liver neoplasms HSDN C4085211 Pain distress question C0154778 Myopia, degenerative HSDN C0013404 Respiratory difficulty C0039981 Thoracic neoplasms HSDN C0041834 Erythematous condition C0867389 Chronic graft-versus-host disease MalaCards C0042963 Symptoms vomiting C0268410 Acid phosphatase deficiency HPO C2984058 Have pain C0026272 Mixed connective tissue disease HSDN C1963170 Hypothermia adverse event C0007789 Cerebral palsy HSDN C0036572 Convulsion C0027927 Neurosyphilis HSDN C2911647 Weight gain adverse event C0002170 Alopecia HSDN C0018681 Headache, cephalalgia C0042769 Virus diseases HSDN C0413252 Hypothermia due to exposure C0342257 Complications of diabetes mellitus HSDN C2919142 Short stature adverse event C0036069 Saldino-noonan syndrome MalaCards C0040822 D tremors C0036323 Schistosomiasis HSDN C4084723 Constipation C3683846 Chromosome 17p deletion syndrome MalaCards C0023380 Lethargy C0027672 Neoplastic syndromes, hereditary HSDN C0557874 Global developmental delay C2931894 Mucolipidosis 2 MalaCards C0151786 Weakness muscle C0002875 Cooley's anemia OrphaNet|HPO C0518090 Frequency of pain question C0497572 Female genital herpes HSDN C0039070 Collapse fleeting C4050613 Anxiety scale (basc-2) HSDN C0398650 Idiopathic thrombocytopenia purpura C0025323 Menorrhagia HSDN C0040264 Ear ringing sound C2984572 Malaria pathway HSDN C1963170 Hypothermia adverse event C0008066 Child behavior disorders HSDN C4085210 Usual severity pain C0024894 Mastitis HSDN C1963087 Constipation adverse event C0042781 Visceral myopathy MalaCards C0030193 Sense of pain C0221002 Hyperparathyroidism, primary HSDN C0009460 Communication impairment C0036363 Schizotypal personality disorder HSDN C0004604 Pain back C0014836 Escherichia coli infections HSDN C0009676 Confusion state C0033927 Psychopathology HSDN C0231528 Muscle pain generalized C0043398 Yellow fever, urban MalaCards C0413252 Hypothermia due to exposure C0517555 Venous thrombosis after immobility HSDN C0587246 Extremity weakness C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C0426579 Anorexia symptom C0043395 Yellow fever DiseaseOntology|OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0012359 Pathological dilatation HSDN C0917816 Deficiency mental C1859568 Bardet-biedl syndrome 10 HPO C4085210 Usual severity pain C0035412 Rhabdomyosarcoma HSDN C0015300 Ocular proptosis C0265218 Neu-laxova syndrome HPO C2919142 Short stature adverse event C3151056 Spastic paraplegia 51, autosomal recessive MalaCards|HPO C4085211 Pain distress question C0242891 Injuries teeth HSDN C4084773 Bothered by weight gain C0085159 Seasonal affective disorder HSDN C0004134 Dyssynergia C0795949 Galloway mowat syndrome HPO C0018524 Hallucinate C0027663 Neoplasms, multiple primary HSDN C0151908 Dry skin C1857053 Ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum OrphaNet|MalaCards C4084784 Diarrhea C0029422 Osteochondrodysplasias HSDN C0240444 Nail thickening C1834340 Leigh syndrome, adult UMLS C0424755 Fever symptoms C0009241 Cognition disorders HSDN C2315100 Pediatric failure to thrive C0796117 Pitt syndrome MalaCards C0018991 Paralysis one side of body C0085278 Antiphospholipid syndrome HSDN C4084769 Vomiting frequency C0162872 Aortic aneurysm, thoracic HSDN C0151825 Ostalgia C1833699 Osteopoikilosis, isolated MalaCards C0020673 Hypothermia (central) (local) C0035801 Diseases rodent HSDN C2029884 Hearing loss by exam C0026896 Myasthenia gravis HSDN C2024893 Cardiovascular surgery result: fatigue C2931518 Plexosarcoma MalaCards C4084769 Vomiting frequency C0079744 Diffuse large b-cell lymphoma HSDN C0027796 Neuralgias C0029443 Osteomyelitis HSDN C3463815 Feel fatigue C0005695 Bladder neoplasm HSDN C0860603 Anxiety symptom C1862939 Amyotrophic lateral sclerosis 1 MalaCards C2984057 Have nausea C0033046 Premenstrual syndrome HSDN C0030193 Sense of pain C0042900 Vitiligo HSDN C0522224 Palsied C0001627 Congenital adrenal hyperplasia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007771 Intracranial arteriosclerosis HSDN C0027066 Myoclonic jerking C0042338 Herpesvirus 3, human HSDN C2984058 Have pain C0031350 Pharyngitis HSDN C4084723 Constipation C0008625 Chromosome aberrations HSDN C4084727 Cough frequency C0243025 Hantavirus pulmonary syndrome MalaCards C1549543 Administration method - pain C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C1963252 Tremor adverse event C0751877 Hereditary central nervous system demyelinating diseases HSDN C1557397 Adverse event associated with pain C0005935 Bone conduction HSDN C0000737 Abdomen pain C0206680 Mesothelioma, cystic OrphaNet|MalaCards C2911647 Weight gain adverse event C0042344 Varicose ulcer HSDN C4084725 Usual severity cough C2609414 Acute kidney injury HSDN C2203646 Jaundice C0027726 Nephrotic syndrome HSDN C3463815 Feel fatigue C0037744 Perceptual spatial orientation HSDN C0018681 Headache, cephalalgia C0042075 Urologic diseases HSDN C3641755 Have constipation C2713392 Phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency HPO C1963137 Hydrocephalus adverse event C0220681 Goldenhar syndrome with ipsilateral radial defect MalaCards C0460137 Push down or depress C1527406 Rhizomelic pseudopolyarthritis MalaCards C3641756 Have diarrhea C0013364 Dysautonomia, familial HPO C4084767 Bothered by vomiting C1705811 Terminology role entity HSDN C3887638 Failure to thrive in infant C2700553 Omenn syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C1862172 Bowing of legs, anterior, with dwarfism MalaCards C1963135 Hepatic necrosis adverse event C0206624 Hepatoblastoma MalaCards C4084775 Usual severity weight loss C0007787 Transient ischemic attack HSDN C0030193 Sense of pain C0011875 Diabetic angiopathies HSDN C3812171 Bradycardia by ecg finding C2939462 Immunoglobulin deposition disease MalaCards C0043352 Absent salivary secretion C0406704 Rudiger syndrome 1 MalaCards|HPO C2315100 Pediatric failure to thrive C0030297 Pancreatic neoplasm HSDN C0518090 Frequency of pain question C0016059 Fibrosis HSDN C4085862 Bothered by nausea C0026865 Mushroom poisoning HSDN C0233514 Behavior abnormal C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet C0036572 Convulsion C0022650 Kidney calculi HSDN C4085210 Usual severity pain C0017574 Gingivitis HSDN C0008031 Pain chest C1851347 Familial mediterranean fever, autosomal dominant HPO|UMLS C0237326 Defecation pain C0346407 Pancreatic polypeptide-oma MalaCards C4084723 Constipation C0002878 Anemia, hemolytic HSDN C0003079 Pupillary inequality C0014121 Bacterial endocarditis HSDN C2984058 Have pain C0033944 Psychosexual development HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1962963 Osteoporosis adverse event HSDN C0086439 Activity decreased C0024121 Lung neoplasms HSDN C1069915 Vertigo C0024904 Mastoiditis HSDN C0000737 Abdomen pain C0041408 Turner syndrome HSDN C0018784 Deafness sensorineural C1854594 Deafness, autosomal dominant 23 MalaCards|HPO C1963170 Hypothermia adverse event C0035358 Retroperitoneal neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0265334 Pachyonychia congenita HSDN C3898969 Have been vomiting C0026636 Mouth diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3244301 Coverage level - family HSDN C4085222 Nausea C0018939 Hematological disease HSDN C2919142 Short stature adverse event C1415737 Hsd11b2 gene HPO C0030214 Myoclonus palatal C0027438 Nasopharynx UMLS C0018772 Deafness C0020443 Hypercholesterolemia HSDN C1557397 Adverse event associated with pain C0010073 Coronary artery vasospasm HSDN C1963091 Diarrhea adverse event C0853698 Lymphocytes increased HSDN C0557874 Global developmental delay C4015495 Cerebellofaciodental syndrome MalaCards C0031911 Pigment deposition C0334583 Pilocytic astrocytoma MalaCards C0151786 Weakness muscle C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards C4084768 Usual severity vomiting C0344434 Atrial fibrillation ecg HSDN C0043144 Wheeze C0810299 Other and unspecified lower respiratory disease UMLS C2024893 Cardiovascular surgery result: fatigue C0238288 Muscular dystrophy, facioscapulohumeral HSDN C4085661 Usual severity nausea C0007125 Carcinoma, ehrlich tumor HSDN C3463815 Feel fatigue C0017636 Glioblastoma MalaCards|HSDN C0018777 Deafness, conductive C0042830 Perception visual HSDN C0424755 Fever symptoms C0008479 Chondrosarcoma HSDN C0085650 Purpura fulminans C1412760 Bckdhb gene HSDN C1963086 Confusion adverse event C0038356 Stomach neoplasms HSDN C2911645 Weight loss adverse event C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C2032396 Pelvic pain on the right C0227791 Discharge vaginal HSDN C0027498 Nausea vomiting C0206138 Crest syndrome OrphaNet|MalaCards C1557397 Adverse event associated with pain C0017510 Gestures HSDN C0151786 Weakness muscle C0035242 Respiratory tract diseases HSDN C3539023 Pelvic pain increasing in frequency C0010356 Cross infection HSDN C4084768 Usual severity vomiting C0162565 Acute intermittent porphyria MalaCards|HSDN|HPO C4084767 Bothered by vomiting C0043167 Pertussis HSDN C0004134 Dyssynergia C3495588 Acrocephalopolydactylous dysplasia MalaCards C0577572 Mass of musculoskeletal structure C0341037 Cyst periodontal lateral UMLS C3146279 Coma C0010054 Coronary arteriosclerosis HSDN C0037771 Paraparesis spastic C0027809 Neurilemmoma HSDN C0184567 Pain acute C0035522 Rib fracture HSDN C0020538 Hbp C0268146 Glucose-6-phosphate transport defect MalaCards|HPO C0042571 Vertigo subjective C0035305 Retinal detachment HSDN C0018926 Emesis bloody C2984299 Asthma pathway HSDN C0234664 Eyelid lag C0751360 Becker generalized myotonia UMLS C2237041 Shox gene with short stature C1856790 Femur fibula ulna syndrome MalaCards C2237041 Shox gene with short stature C1865208 Anal atresia, hypospadias, and penoscrotal inversion MalaCards C0027497 Queasy C0011860 Diabetes mellitus, non-insulin-dependent UMLS C0424755 Fever symptoms C0887833 Carcinoma, pancreatic ductal HSDN C0151786 Weakness muscle C0460137 Push down or depress HSDN C4085549 Dizziness C0007222 Cardiovascular diseases HSDN C2911645 Weight loss adverse event C0041327 Tuberculosis, pulmonary HSDN C3887638 Failure to thrive in infant C1852576 Copper deficiency, familial benign MalaCards C3463815 Feel fatigue C1848410 Xeroderma pigmentosum, variant type MalaCards C0030486 Extremity paralysis, lower C0023441 Leukemia, experimental HSDN C1963086 Confusion adverse event C0872996 Q fever vaccine HSDN C1962972 Proteinuria adverse event C1858361 Pyogenic arthritis, pyoderma gangrenosum and acne MalaCards|HPO C4085211 Pain distress question C0042133 Uterine fibroids HSDN C0007398 Catatonic C3274850 Id1 wt allele HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014008 Empty sella syndrome HSDN C0033377 Caudal displacement C2751878 Hadziselimovic syndrome MalaCards C1962972 Proteinuria adverse event C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C1963184 Nystagmus adverse event C0342436 Diencephalic syndrome OrphaNet|MalaCards C0020505 Excessive eating C0033871 Psychiatric status rating scales HSDN C1557397 Adverse event associated with pain C0040948 Trichostrongyliasis HSDN C0085631 Abnormal excitement C1881674 Medical device emits smoke HSDN C0009421 Comatose C0037930 Spinal cord neoplasms HSDN C0151818 Opisthotonos C1854988 Molybdenum cofactor deficiency, complementation group a HPO|UMLS C2242996 Tingling C0032533 Polymyalgia rheumatica MalaCards C0086565 Liver function abnormal C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0239574 Fever low grade C0238990 Acute lower respiratory tract infection MalaCards C0270948 Neurogenic muscular atrophy C1836916 Posterior column ataxia with retinitis pigmentosa HPO C2315100 Pediatric failure to thrive C0001198 Disease pink HSDN C4085210 Usual severity pain C0004144 Atelectasis HSDN C0851578 Disorder sleep C0236733 Amphetamine-related disorders HSDN C0032227 Effusion pleural C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0028738 Nystagmus C0546878 Salaam spasms MalaCards C0019825 Voice hoarseness C0175702 Williams syndrome OrphaNet|HPO|MalaCards C1963066 Joint pain adverse event C1838280 Epiphyseal dysplasia, multiple, 1 MalaCards C2203646 Jaundice C0039730 Thalassemia HSDN C3665492 Pigmentations C3896578 Familial colorectal cancer type x MalaCards C0242936 Center pain C0035189 Residential treatment HSDN C1959630 Eye pain adverse event C0035320 Retinal neovascularization HSDN C0349506 Sun sensitivity C0265201 De sanctis-cacchione syndrome MalaCards|HPO C4084727 Cough frequency C0037304 Skull fracture HSDN C0027497 Queasy C0018824 Heart valve disease HSDN C3641755 Have constipation C0026850 Muscular dystrophy HSDN C1384666 Decreased hearing C2675486 Chromosome 6pter p24 deletion syndrome OrphaNet|MalaCards C1963093 Dizziness adverse event C0040100 Thymoma HSDN C3887873 Hearing loss C0037397 Behavior social HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1963266 Uveitis adverse event HSDN C0015970 Fever unknown origin C2609414 Acute kidney injury HSDN C0015672 Decreased energy C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) MalaCards C3887638 Failure to thrive in infant C0342873 Glutaric aciduria iii MalaCards|HPO C0009676 Confusion state C0022658 Kidney diseases HSDN C3541349 Syncope C0085277 Munchausen by proxy syndrome HSDN C0349588 Stature short C1859405 Bowen-conradi syndrome OrphaNet|HPO|MalaCards C3641755 Have constipation C0042373 Vascular diseases HSDN C0030200 Intractable pain C0022665 Kidney neoplasm HSDN C1000483 Genus anemia C0524988 Schnitzler syndrome OrphaNet|MalaCards C0231218 Malaise generalized C3273127 Extrahepatic bile duct adenocarcinoma, gastric foveolar type UMLS C0013421 Dystonia C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0030193 Sense of pain C0752308 Hypoxia-ischemia, brain HSDN C0151889 Reflexes tendon increased C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C2237041 Shox gene with short stature C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C4084769 Vomiting frequency C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C0004604 Pain back C0019294 Hernia, inguinal HSDN C0015672 Decreased energy C0010054 Coronary arteriosclerosis HSDN C3665347 Vision impaired C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0025284 Meningeal neoplasms MalaCards|HSDN C1263846 Attention deficit disorder with hyperactivity C3683846 Chromosome 17p deletion syndrome MalaCards C3539020 Pelvic pain decreasing in frequency C0027765 Nervous system disorder HSDN C0013362 Dysarthrias C0302148 Blood clot HSDN C2315100 Pediatric failure to thrive C3809971 Asparagine synthetase deficiency MalaCards C0043094 Weight gain C0024305 Lymphoma, non-hodgkin HSDN C0019825 Voice hoarseness C1708954 Mediastinal germ cell tumor with somatic-type malignancy UMLS C0349588 Stature short C0472813 X-linked agammaglobulinemia with growth hormone deficiency HPO C0018777 Deafness, conductive C1863389 Apert-crouzon disease MalaCards C0020580 Decreased sensation C0016507 Acquired foot deformities HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0428977 Bradycardia HSDN C0151205 Periorbital edema C0268263 Multiple sulfatase deficiency disease MalaCards|HPO|UMLS C4085211 Pain distress question C0026847 Spinal muscular atrophy HSDN C2919142 Short stature adverse event C3151440 Pituitary hormone deficiency, combined, 6 MalaCards|HPO C3641756 Have diarrhea C0238027 Botulism, infantile MalaCards C2984058 Have pain C0030215 Palate tumor HSDN C0042963 Symptoms vomiting C0043168 Whooping cough due to unspecified organism HSDN C0022107 Fussiness C2936917 Infantile polyarteritis MalaCards C2919142 Short stature adverse event C3151140 Pontocerebellar hypoplasia, type 2d MalaCards C4084802 Usual severity diarrhea C0032227 Pleural effusion disorder HSDN C2911645 Weight loss adverse event C0027666 Neoplasms, radiation-induced HSDN C2911645 Weight loss adverse event C0020676 Hypothyroidism HSDN C4084727 Cough frequency C1279945 Acute interstitial pneumonia MalaCards C2919142 Short stature adverse event C1862130 Brachydactyly type a6 MalaCards C0031256 Petechia C0398650 Immune thrombocytopenic purpura OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0014121 Bacterial endocarditis HSDN C3887784 Decreased urine output C0000832 Abruptio placentae HSDN C0030193 Sense of pain C0043241 Wound infection HSDN C0018772 Deafness C2936346 22q11 deletion syndrome OrphaNet C3641756 Have diarrhea C0043194 Wiskott-aldrich syndrome MalaCards C0575081 Abnormal gait C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C0917801 Sleep disorder insomnia C0852928 Exacerbated insomnia UMLS C0013404 Respiratory difficulty C0027627 Neoplasm metastasis HSDN C1963170 Hypothermia adverse event C3244301 Coverage level - family HSDN C0020673 Hypothermia (central) (local) C0032914 Pre-eclampsia HSDN C0026838 Spasticity muscle C1866770 Spinocerebellar ataxia with rigidity and peripheral neuropathy UMLS C3815497 Cough C0007121 Bronchogenic carcinoma HSDN C4084776 Weight loss C0020507 Hyperplasia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019556 Canine hip dysplasia HSDN C0521800 Central cyanosis C0037274 Dermatologic disorders UMLS C2984058 Have pain C0009187 Coccidiosis HSDN C0030554 Abnormal sensation C0751194 Hematoma, spinal subdural HSDN C0040822 D tremors C0033941 Psychoses, substance-induced HSDN C0235153 Sensory hallucination C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C0233514 Behavior abnormal C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0018772 Deafness C0004106 Astigmatism HSDN C3541349 Syncope C0009375 Colonic neoplasms HSDN C0494475 Seizure generalized tonic clonic C2751756 Febrile convulsions, familial, 3a HPO C0151889 Reflexes tendon increased C0342777 Succinate-coenzyme q reductase deficiency MalaCards C0018808 Murmur C0796561 Melanoma vaccines HSDN C0022346 Yellow skin C0524909 Hepatitis b, chronic MalaCards|HSDN C3887784 Decreased urine output C0752308 Hypoxia-ischemia, brain HSDN C3665347 Vision impaired C1858301 Leber congenital amaurosis 5 MalaCards|HPO C0012833 Dizzy C0001144 Acne vulgaris HSDN C3641755 Have constipation C0006118 Brain neoplasms HSDN C0518090 Frequency of pain question C0014556 Epilepsy, temporal lobe HSDN C4084775 Usual severity weight loss C0029456 Osteoporosis HSDN C0155047 Visual loss, both eyes unqual. C0015397 Disorder of eye UMLS C1963137 Hydrocephalus adverse event C1866256 Coloboma-obesity-hypogenitalism-mental retardation syndrome MalaCards C0851578 Disorder sleep C0000833 Abscess HSDN C0015469 Facial paralysis C0282160 Aplasia cutis congenita MalaCards|HPO C3815497 Cough C0018800 Cardiomegaly HSDN C4042891 Sleep wake disorders C0027666 Neoplasms, radiation-induced HSDN C0003862 Pain joint C3812646 Drug induced cutaneous vasculitis MalaCards C0003862 Pain joint C0282687 Hemorrhagic fever, ebola DiseaseOntology|OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0878544 Cardiomyopathies HSDN C4085211 Pain distress question C0162871 Aortic aneurysm, abdominal HSDN C0004604 Pain back C0003962 Ascites HSDN C1963093 Dizziness adverse event C0043253 Trauma blunt HSDN C0030193 Sense of pain C0027720 Nephrosis HSDN C0015970 Fever unknown origin C0009952 Febrile convulsions HSDN C0015672 Decreased energy C0018801 Heart failure HSDN C0231528 Muscle pain generalized C0340992 Cryoglobulinemic; vasculitis OrphaNet|MalaCards C0000727 Abdomen acute C0018798 Congenital heart defects HSDN C0018681 Headache, cephalalgia C0040411 Tongue neoplasms HSDN C3641756 Have diarrhea C2937421 Prostatic hyperplasia HSDN C4084774 Have weight loss C0085655 Polymyositis OrphaNet|MalaCards C2169806 Tic C2713543 Biofeedback eeg HSDN C0015468 Face pain C0458219 Complex regional pain syndromes HSDN C4084773 Bothered by weight gain C0014394 Enuresis HSDN C1963154 Renal failure adverse event C3151568 Nephrotic syndrome, type 4 MalaCards C0242936 Center pain C0037072 Diseases sigmoid HSDN C1962972 Proteinuria adverse event C0042338 Herpesvirus 3, human HSDN C0012833 Dizzy C0085183 Neoplasms, second primary HSDN C0012833 Dizzy C0021603 Sleep initiation and maintenance disorders HSDN C0009806 Constipate C0003125 Anorexia nervosa HSDN C0013421 Dystonia C0268275 Tay-sachs disease, ab variant MalaCards C0042963 Symptoms vomiting C0023817 Hyperlipoproteinemia type i HPO C3898969 Have been vomiting C0152942 Enteric tularemia nos DiseaseOntology|MalaCards C1557397 Adverse event associated with pain C0151526 Premature birth HSDN C0042940 Disorder of voice C0007820 Cerebrovascular disorders HSDN C0010520 Skin cyanosis C1389016 Atrioventricular canal defect HPO C0030486 Extremity paralysis, lower C0236969 Substance-related disorders HSDN C2315100 Pediatric failure to thrive C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C0497247 Blood pressure elevation C0342859 Harderoporphyria HPO C0036572 Convulsion C0037072 Diseases sigmoid HSDN C4084774 Have weight loss C0473876 Cryptogenic tularaemia MalaCards C0426579 Anorexia symptom C0011581 Depressive disorder HSDN C0030552 Paralysis partial C0038395 Streptococcal infections HSDN C1963091 Diarrhea adverse event C0085136 Central nervous system neoplasms HSDN C0020438 Hypercalciuria C0028860 Oculocerebrorenal syndrome OrphaNet|HSDN|HPO C0264588 Dysphonia spasmodic C2677567 Dystonia 16 (disorder) MalaCards C3541349 Syncope C0041948 Uremia HSDN C0036659 Sensation disorder C0040136 Thyroid neoplasm HSDN C0010200 Cough symptom C0242459 Simple pulmonary eosinophilia UMLS C0043068 Friderichsen-waterhouse syndrome C0001403 Addison disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0026266 Mitral valve insufficiency HSDN C0013604 Edematous C0032708 Disorders of porphyrin metabolism HSDN C0557874 Global developmental delay C1843891 Spinocerebellar ataxia 21 HPO C0022638 Ketosis C1855109 Methylmalonic aciduria cbla type HPO C2911645 Weight loss adverse event C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0242658 Homosexuality male HSDN C4084784 Diarrhea C0024530 Malaria HSDN C0018772 Deafness C0023269 Leiomyosarcoma HSDN C0020796 Profoundly mentally retarded C1848650 Ulnar hypoplasia with mental retardation MalaCards C2984058 Have pain C0013298 Duodenitis HSDN C4085862 Bothered by nausea C0020875 Ileal diseases HSDN C1963170 Hypothermia adverse event C2984289 Melanoma pathway HSDN C2019869 Staring spells C3279793 Combined oxidative phosphorylation deficiency 8 MalaCards|UMLS C0027796 Neuralgias C0039980 Chest injury HSDN C0018775 Hearing loss bilateral C0011570 Mental depression HSDN C0009806 Constipate C0235387 Porphyria type syndrome OrphaNet C0009792 Consciousness disorder C0040127 Thyroid crisis HSDN C3541349 Syncope C1970298 Progressive familial heart block, type ib MalaCards|HPO C2203646 Jaundice C0024141 Lupus erythematosus, systemic HSDN C0426579 Anorexia symptom C0042470 Guanarito haemorrhagic fever MalaCards C0039070 Collapse fleeting C0027746 Nerve degeneration HSDN C1963091 Diarrhea adverse event C1258104 Diffuse scleroderma HSDN C0520966 Coordination impaired C1851708 Encephalopathy, recurrent, of childhood MalaCards|UMLS C2096293 Ent surgical result ear vertigo C0020676 Hypothyroidism HSDN C0022107 Fussiness C4014488 Pontocerebellar hypoplasia, type 2e MalaCards C0011570 Monopolar depression C0334123 Histiocytosis, lipoid MalaCards C0850758 Pain pelvic C0002989 Epithelioid hemangioma of skin HSDN C0015970 Fever unknown origin C0027121 Myositis HSDN C1963087 Constipation adverse event C0014805 Primary erythermalgia MalaCards|HPO C0018784 Deafness sensorineural C0020676 Hypothyroidism HSDN C0036572 Convulsion C0220989 Acquired partial lipodystrophy OrphaNet|HPO|MalaCards C0009421 Comatose C0043251 Wounds and injuries HSDN C1313921 Urinomas C0037073 Sigmoid neoplasms HSDN C0917816 Deficiency mental C3494506 Pseudohypoparathyroidism, type ia OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0149931 Migraine disorders MalaCards C1999266 Depression adverse event C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO C4084768 Usual severity vomiting C0003811 Cardiac arrhythmia HSDN C0007758 Cerebellar ataxia C0206245 Amyloid neuropathies, familial MalaCards C0009806 Constipate C0034069 Pulmonary fibrosis HSDN C0234378 Postural tremor C1839780 Fragile x tremor/ataxia syndrome MalaCards|HPO|UMLS C4084724 Usual severity constipation C0595812 Fistula route HSDN C0085631 Abnormal excitement C0021400 Influenza HSDN C0015300 Ocular proptosis C1956097 Wolf-hirschhorn syndrome MalaCards|HPO C0036572 Convulsion C0393672 Benign psychomotor epilepsy, childhood UMLS C0015672 Decreased energy C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C0026826 High muscle tone C0752355 Myotonia fluctuans (disorder) OrphaNet|HPO C4084769 Vomiting frequency C1704326 Role - roleclass HSDN C1963184 Nystagmus adverse event C1859564 Bardet-biedl syndrome 3 HPO C0015469 Facial paralysis C1253943 Fluid in the chest HSDN C0003862 Pain joint C0001175 Acquired immunodeficiency syndrome HSDN C4084767 Bothered by vomiting C0015802 Femur fracture HSDN C3539891 Pelvic pain to the rear C0000768 Congenital abnormality HSDN C0575081 Abnormal gait C1846790 Joubert syndrome 4 (disorder) MalaCards C0029163 Hemorrhage mouth C0040038 Thromboembolism HSDN C4084773 Bothered by weight gain C0031149 Peritoneal neoplasms HSDN C0042024 Urine incontinence C0403447 Chronic kidney insufficiency HSDN C0036572 Convulsion C0343108 Flynn aird syndrome OrphaNet|MalaCards C0030552 Paralysis partial C3150754 Glycogen storage disease xv MalaCards|HPO C1069915 Vertigo C0015414 Eye neoplasms HSDN C4085317 Diarrhea frequency C0001206 Acromegaly HSDN C4084773 Bothered by weight gain C0085183 Neoplasms, second primary HSDN C3815497 Cough C0025202 Melanoma HSDN C0013390 Cramps menstrual C1963198 Pancreatitis adverse event HSDN C0036572 Convulsion C1547046 Kind of quantity - taste HSDN C0151825 Ostalgia C2347507 Philadelphia positive childhood acute lymphoblastic leukemia UMLS C0010200 Cough symptom C1546635 Specimen source codes - fistula HSDN C4084784 Diarrhea C0026857 Musculoskeletal diseases HSDN C2984058 Have pain C1321581 Bezoar disorder HSDN C0018681 Headache, cephalalgia C0030920 Peptic ulcer HSDN C0030193 Sense of pain C0036986 Shock, traumatic HSDN C1963093 Dizziness adverse event C0017168 Gastroesophageal reflux disease HSDN C0009421 Comatose C1859974 Glucocorticoid deficiency 1 HPO C0036572 Convulsion C0029089 Ophthalmoplegia MalaCards C0003079 Pupillary inequality C0020458 Hyperhidrosis disorder HSDN C0042940 Disorder of voice C0004404 Autosuggestion HSDN C0040034 Thrombocytopenia C1855057 Ataxia-telangiectasia variant v2 HPO C0427068 Legs weakness C1863704 Spastic paraplegia 8, autosomal dominant MalaCards|HPO C0242936 Center pain C0010967 Behavior, dangerous HSDN C4084727 Cough frequency C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C0022346 Yellow skin C0027145 Myxedema HSDN C4085661 Usual severity nausea C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0027796 Neuralgias C0595812 Fistula route HSDN C0000737 Abdomen pain C0854787 Non-resectable carcinoma of small bowel UMLS C4084773 Bothered by weight gain C2937421 Prostatic hyperplasia HSDN C4084766 Vomiting C0948039 Bacterial gastritis MalaCards C0037384 Snore C0035258 Restless legs syndrome HSDN C0030486 Extremity paralysis, lower C0037313 Sleep HSDN C1963170 Hypothermia adverse event C0006109 Brain damage, chronic HSDN C0018681 Headache, cephalalgia C3661735 Basilar artery migraine, intractable UMLS C0005745 Blepharoptosis C0272309 Simple bruising MalaCards C2242996 Tingling C0039082 Syndrome HSDN C2237041 Shox gene with short stature C2749685 Cystinosis, atypical nephropathic (disorder) HPO C0851578 Disorder sleep C0236664 Alcohol-related disorders HSDN C1557397 Adverse event associated with pain C0376634 Craniofacial abnormalities HSDN C4082202 Sleep quality question C3178970 Entrapment, pudendal nerve MalaCards C0232476 Absent peristalsis C0267067 Esophageal aperistalsis UMLS C2096293 Ent surgical result ear vertigo C0033578 Prostatic neoplasms HSDN C3887638 Failure to thrive in infant C0033300 Progeria OrphaNet|HSDN|HPO C0033774 Skin pruritus C0019163 Hepatitis b HSDN C2984058 Have pain C0021359 Infertility HSDN C0040822 D tremors C0001624 Adrenal gland neoplasms HSDN C0454644 Delayed language development C0432267 Tricho thiodystrophy disorder MalaCards C0019214 Hepatosplenomegaly C1853392 Interleukin 2 receptor, alpha, deficiency of MalaCards|HPO C0917816 Deficiency mental C0796244 Mental retardation, x-linked, with or without seizures, arx-related (disorder) HPO C0085636 Light sensitivity C0282504 Environmental allergies HSDN C4084802 Usual severity diarrhea C0027627 Neoplasm metastasis HSDN C0020538 Hbp C1567743 Alport syndrome, autosomal dominant MalaCards|HPO C4085211 Pain distress question C0007135 Adenocarcinoma, scirrhous HSDN C0027497 Queasy C0021295 Infant, premature, diseases HSDN C0518090 Frequency of pain question C0043168 Whooping cough due to unspecified organism HSDN C0030193 Sense of pain C0010308 Congenital hypothyroidism HSDN C0012833 Dizzy C0751908 Vestibular neuronitis UMLS C0006370 Bulimia C0030974 Perceptual defense HSDN C0036572 Convulsion C0017205 Gaucher disease HSDN C4085317 Diarrhea frequency C0036329 Schistosomiasis japonica DiseaseOntology C0030232 Color loss C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C0042963 Symptoms vomiting C0021359 Infertility HSDN C1557397 Adverse event associated with pain C0149887 Slipped capital femoral epiphyses HSDN C0034150 Skin purpura C0428953 Ecg infarction myocardial HSDN C3539895 Pelvic pain occurs with bowel movement C0038478 Struma ovarii HSDN C3665347 Vision impaired C1833321 Chorioretinal atrophy, progressive bifocal OrphaNet|MalaCards C0026205 Pupillary constriction C0038986 Sweat gland diseases HSDN C0036572 Convulsion C1832916 Timothy syndrome MalaCards C0700590 Diaphoresis excessive C0034065 Pulmonary embolism UMLS C4084769 Vomiting frequency C0302148 Blood clot HSDN C0518090 Frequency of pain question C0032816 Post-concussion headache HSDN C4084742 Bothered by night sweats C0036467 Scrofula MalaCards C3274924 Have been coughing C0042373 Vascular diseases HSDN C4084774 Have weight loss C0036946 Sheep--diseases HSDN C0018991 Paralysis one side of body C0700327 Clinical findings relating to memory HSDN C3539889 Pelvic pain increasing in severity C2936631 Complaint, subjective health HSDN C0312416 Morning sickness C0266836 Infantile colic HSDN C0035229 Respiratory function impaired C0238357 Hyperkalemic periodic paralysis HPO C0344434 Atrial fibrillation ecg C1834481 Cardiomyopathy, dilated, 1s MalaCards C0009676 Confusion state C0001807 Aggressive behavior HSDN C0427055 Face weakness C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia HPO C4085211 Pain distress question C0198632 Pneumoperitoneum HSDN C0917801 Sleep disorder insomnia C0270540 Insomnia, mixed UMLS C0011570 Monopolar depression C0010481 Cushing syndrome OrphaNet C0036572 Convulsion C0037379 Snake bite HSDN C0460137 Push down or depress C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C0575081 Abnormal gait C2930923 N-acetylneuraminic acid storage disease MalaCards C0518090 Frequency of pain question C0021603 Sleep initiation and maintenance disorders HSDN C0151205 Periorbital edema C2931916 Midline granulomatosis MalaCards C4085210 Usual severity pain C0006285 Bronchopneumonia HSDN C4084725 Usual severity cough C0003864 Arthritis HSDN C0042798 Vision dim C1862596 Familial hypobetalipoproteinemia MalaCards C0039070 Collapse fleeting C1838527 Long qt syndrome 3, acquired, susceptibility to HPO C2237041 Shox gene with short stature C0027831 Neurofibromatosis 1 HPO C0002622 Amnesias C3244301 Coverage level - family HSDN C0018784 Deafness sensorineural C1414203 Dws gene HSDN C0030200 Intractable pain C0011265 Presenile dementia HSDN C4085211 Pain distress question C0027626 Neoplasm invasiveness HSDN C1963184 Nystagmus adverse event C3810080 Mental retardation, autosomal recessive 40 MalaCards C0002170 Alopecia disorders C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C1963184 Nystagmus adverse event C2677903 Mental retardation and microcephaly with pontine and cerebellar hypoplasia OrphaNet|HPO|MalaCards C0349588 Stature short C2932716 Pseudohypoparathyroidism type 1c OrphaNet|HPO C0042963 Symptoms vomiting C0016483 Food preferences HSDN C1145670 Failure respiratory C0268328 Porphobilinogen synthase deficiency MalaCards C0000727 Abdomen acute C0036631 Seminoma HSDN C0022346 Yellow skin C3714644 Thymus neoplasms HSDN C0917816 Deficiency mental C0796099 Cleft lip-palate with abnormal thumbs and microcephaly MalaCards C0085631 Abnormal excitement C0029944 Drug overdose HSDN C1549543 Administration method - pain C0031069 Familial mediterranean fever HSDN C4084769 Vomiting frequency C0206644 Histiocytoma, benign fibrous HSDN C0011991 Loose stools C0022548 Keloid HSDN C0009806 Constipate C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0014724 Burping C0001173 Adult pyloric stenosis HSDN C0042963 Symptoms vomiting C0524812 Intracranial hypotension HSDN C1971624 Appetite absent C0152164 Cyclical vomiting syndrome (disorder) MalaCards C4084784 Diarrhea C0085435 Arthritis, reactive OrphaNet|MalaCards C1963086 Confusion adverse event C0008350 Cholelithiasis HSDN C2911645 Weight loss adverse event C0023364 Leptospirosis HSDN C4085549 Dizziness C0013080 Down syndrome HSDN C0043094 Weight gain C0032002 Pituitary diseases HSDN C0150055 Pain chronic C1720894 Genitourinary disease, male HSDN C0010520 Skin cyanosis C0032298 Lipid pneumonia HSDN C0241137 Skin pallor C0042373 Vascular diseases HSDN C0025287 Meningitis-like C0001957 Alcohol withdrawal delirium HSDN C0033774 Skin pruritus C2987139 Pancreatic well differentiated ductal adenocarcinoma UMLS C0242936 Center pain C1704212 Embolism embolus HSDN C0013362 Dysarthrias C1868681 Dystonia 12 HPO C4084784 Diarrhea C0025294 Meningococcal meningitis HSDN C0033774 Skin pruritus C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C0016204 Fart C0042251 Vaginal diseases HSDN C0013395 Indigestion C0007097 Carcinomas HSDN C2830339 Other polyuria C0042075 Urologic diseases UMLS C1963065 Apnea adverse event C0021603 Sleep initiation and maintenance disorders HSDN C0917816 Deficiency mental C2675473 Mental retardation, autosomal dominant 5 MalaCards|HPO C0018524 Hallucinate C2586211 Thrombosis of blood vessel HSDN C0557874 Global developmental delay C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|HPO|MalaCards C4084776 Weight loss C0030920 Peptic ulcer HSDN C4084802 Usual severity diarrhea C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0036659 Sensation disorder C0042338 Herpesvirus 3, human HSDN C0232466 Feeding difficulty C3711125 Mitochondrial dna depletion syndrome 8a MalaCards C0036572 Convulsion C1963282 Wolff-parkinson-white syndrome adverse event HSDN C0034155 Thrombotic thrombocytopenic purpura C0812393 Cancer patients and suicide and depression HSDN C0034151 Hyperglobulinemic purpura C0003864 Arthritis HSDN C0030486 Extremity paralysis, lower C0006147 Breast fed HSDN C1963087 Constipation adverse event C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0011168 Disorder deglutition C2677565 Amyotrophic lateral sclerosis 10 (disorder) HPO C4085210 Usual severity pain C0079731 B-cell lymphomas HSDN C4084802 Usual severity diarrhea C1257915 Intestinal polyposis HSDN C1999266 Depression adverse event C0002986 Fabry disease MalaCards|HPO C0151686 Growth retardation C3280452 Spinocerebellar ataxia, autosomal recessive 12 MalaCards C0013404 Respiratory difficulty C1553188 Hemolysis - observation HSDN C4085661 Usual severity nausea C0009062 Clostridia infection HSDN C0004134 Dyssynergia C0004610 Bacteremia HSDN C0023530 Leukopenia C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C4084768 Usual severity vomiting C1548484 Rheumatic fever vaccine HSDN C3203358 Alveolar hypoventilation C0032226 Pleural diseases HSDN C0460137 Push down or depress C1963674 Spinocerebellar ataxia 10 MalaCards|HPO C4084725 Usual severity cough C0002874 Aplastic anemia HSDN C4084788 Have dizziness C0004936 Mental disorders HSDN C0015300 Ocular proptosis C3151446 Nestor-guillermo progeria syndrome MalaCards|HPO C4084726 Distress cough C0000833 Abscess HSDN C0460137 Push down or depress C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C1963170 Hypothermia adverse event C0008626 Congenital chromosomal disease HSDN C1963249 Tinnitus adverse event C0814263 Meditation therapy HSDN C0011991 Loose stools C0392622 Toxic effect of carbon tetrachloride HSDN C0019079 Bloody sputum C0011334 Dental caries HSDN C0040485 Wryneck C1846707 Spinocerebellar ataxia 17 OrphaNet|HPO|MalaCards C4084766 Vomiting C0025281 Meniere disease HSDN C2183784 Otorrhea, left ear C0810000 Other ear and sense organ disorders UMLS C4084773 Bothered by weight gain C0022806 Kwashiorkor HSDN C0037763 Spasm C0023676 Life style HSDN C0162834 Hyperpigmentation C1148551 X-linked dyskeratosis congenita MalaCards|HPO C4085549 Dizziness C0007134 Renal cell carcinoma HSDN C1963281 Vomiting adverse event C0042514 Tachycardia, ventricular HSDN C0039070 Collapse fleeting C0032914 Pre-eclampsia UMLS C0042571 Vertigo subjective C0008325 Cholecystitis HSDN C4085548 Usual severity dizziness C0039082 Syndrome HSDN C1557397 Adverse event associated with pain C1963107 Euphoria adverse event HSDN C3541349 Syncope C0023470 Myeloid leukemia HSDN C1963170 Hypothermia adverse event C0011175 Dehydration HSDN C0020505 Excessive eating C0005887 Disorder body image HSDN C1557397 Adverse event associated with pain C0018818 Ventricular septal defects HSDN C0007758 Cerebellar ataxia C1301362 Lymphoma, primary cutaneous anaplastic large cell HSDN C1961131 Cough adverse event C0006277 Bronchitis MalaCards C1963066 Joint pain adverse event C0276386 Mosquito-borne viral fever, oropouche MalaCards C0518090 Frequency of pain question C1175175 Severe acute respiratory syndrome HSDN C2315100 Pediatric failure to thrive C1859537 Bare lymphocyte syndrome, type ii, complementation group d HPO C0013395 Indigestion C0002892 Anemia, pernicious HSDN C2984057 Have nausea C4042784 Feeding and eating disorders HSDN C0917816 Deficiency mental C0268642 Histidinuria renal tubular defect OrphaNet|MalaCards C4085210 Usual severity pain C3809899 Episodic pain syndrome, familial, 3 MalaCards C1279888 Proteinuria of undiagnosed cause C1609433 Congenital absence of kidneys syndrome MalaCards|HPO C4042891 Sleep wake disorders C0024305 Lymphoma, non-hodgkin HSDN C2242996 Tingling C0015379 Extravasation of diagnostic and therapeutic materials HSDN C4084774 Have weight loss C1881600 Malignant vipoma MalaCards C3665347 Vision impaired C0338508 Optic atrophy, autosomal dominant MalaCards|HPO C0206160 Retic count elevated C0001126 Renal tubular acidosis HSDN C4085642 Level of joint stiffness C0039743 Thanatophoric dysplasia MalaCards C0018989 Paresis of one side of body C0025284 Meningeal neoplasms MalaCards C0000727 Abdomen acute C0014556 Epilepsy, temporal lobe HSDN C0595939 Stillborn C0265282 Fibrochondrogenesis HPO C0270948 Neurogenic muscular atrophy C1837728 Amyotrophic lateral sclerosis 8 (disorder) MalaCards|HPO C0034933 Abnormal reflexes C0175754 Agenesis of corpus callosum HSDN C4085211 Pain distress question C1852551 Epithelial recurrent erosion dystrophy MalaCards|HPO C3898969 Have been vomiting C0870082 Hyperkeratosis HSDN C0027497 Queasy C0024788 Green monkey virus disease DiseaseOntology|MalaCards C2919142 Short stature adverse event C0268412 Infantile hypophosphatasia MalaCards C4084768 Usual severity vomiting C0004610 Bacteremia HSDN C1279888 Proteinuria of undiagnosed cause C0001768 Agammaglobulinemia HSDN C1549543 Administration method - pain C0019624 Histiocytosis, non-langerhans-cell HSDN C3887873 Hearing loss C0001430 Adenoma HSDN C0026884 Muteness C0033944 Psychosexual development HSDN C0042963 Symptoms vomiting C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C2024893 Cardiovascular surgery result: fatigue C0006309 Brucellosis DiseaseOntology|HSDN|MalaCards C1963086 Confusion adverse event C0030472 Paraneoplastic syndromes HSDN C4085211 Pain distress question C0032460 Polycystic ovary syndrome HSDN C4085862 Bothered by nausea C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C0221184 Hemianopsia bitemporal C0032001 Pituitary apoplexy OrphaNet|MalaCards C4020887 Photodysphoria C3495483 Amish brittle hair syndrome MalaCards C0013595 Eczematous dermatitis C3150191 Coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities MalaCards|HPO C2984058 Have pain C1522057 Acute enteritis of the mouse intestinal tract HSDN C2096293 Ent surgical result ear vertigo C1865323 Migraine, familial basilar HPO C0242936 Center pain C0009240 Cognition HSDN C0035078 Failure kidney C1862683 Townes brocks branchiootorenal like syndrome HPO C4084726 Distress cough C0011334 Dental caries HSDN C1963071 Back pain adverse event C0040046 Thrombophlebitis HSDN C0009421 Comatose C1412760 Bckdhb gene HSDN C3898969 Have been vomiting C0022890 Labyrinthine disorder HSDN C0004134 Dyssynergia C1548578 Location characteristic id - smoking HSDN C4084724 Usual severity constipation C0009450 Disease caused by microorganism HSDN C0026838 Spasticity muscle C0027663 Neoplasms, multiple primary HSDN C0413252 Hypothermia due to exposure C0027686 Pathologic neovascularization HSDN C4084769 Vomiting frequency C0042487 Venous thrombosis HSDN C4084784 Diarrhea C0012819 Diverticular disease of colon HSDN C1963087 Constipation adverse event C1394494 Cystocele, unspecified HSDN C0917816 Deficiency mental C2930897 Ben ari shuper mimouni syndrome OrphaNet|MalaCards C4084766 Vomiting C0023283 Leishmaniasis, cutaneous HSDN C0011991 Loose stools C0473778 Neonatal chloridorrhea UMLS C0005745 Blepharoptosis C1970106 Bpes, type i, autosomal recessive HPO C4084775 Usual severity weight loss C0221026 X-linked agammaglobulinemia HPO C0015676 Mental fatigue C4085311 Depression - recess HSDN C0011991 Loose stools C2717906 Hereditary angioedema type i HPO|UMLS C0039070 Collapse fleeting C0026896 Myasthenia gravis HSDN C0040034 Thrombocytopenia C0028326 Noonan syndrome MalaCards C0497406 Over weight C1956089 Osteophyte HSDN C4084802 Usual severity diarrhea C1366464 F9 gene HSDN C0009806 Constipate C1866294 Ehlers-danlos syndrome, musculocontractural type 1 HPO|UMLS C3463815 Feel fatigue C0003850 Arteriosclerosis HSDN C4084723 Constipation C0011334 Dental caries HSDN C0036659 Sensation disorder C0018674 Head trauma HSDN C0007814 Cerebrospinal fluid otorrhea C0022738 Klippel-feil syndrome HSDN C0036572 Convulsion C1864663 Hypomyelination and congenital cataract MalaCards C0015970 Fever unknown origin C0023434 Chronic lymphocytic leukemia HSDN C0162298 Stiffness joints C3839326 Kuskokwim syndrome MalaCards C0040822 D tremors C0206255 Malaria vaccine HSDN C1963091 Diarrhea adverse event C0343387 Enterocolitis, neutropenic HSDN C2024878 Cardiovascular surgery result: dyspnea C0037304 Skull fracture HSDN C0030193 Sense of pain C0027877 Neuronal ceroid-lipofuscinoses HSDN C2024878 Cardiovascular surgery result: dyspnea C0577620 Nut hypersensitivity HSDN C0019079 Bloody sputum C0206703 Carcinoma, giant cell HSDN C0700078 Deep tendon reflex decrease C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0016382 Cutaneous vascular engorgement C2364040 Impaired thermoregulation UMLS C4084775 Usual severity weight loss C0232488 Abdominal colic HSDN C2029884 Hearing loss by exam C0015806 Femur neck fracture HSDN C4084802 Usual severity diarrhea C0019069 Hemophilia a HSDN C4085210 Usual severity pain C2936664 Acquired hypogammaglobulinemia HSDN C0042963 Symptoms vomiting C0029134 Optic neuritis HSDN C0518090 Frequency of pain question C0008533 Hemophilia b HSDN C3203358 Alveolar hypoventilation C0027819 Neuroblastoma HSDN C0036572 Convulsion C0206307 Canavan disease MalaCards C4084727 Cough frequency C2117118 X-ray of toe: deformity contracture HSDN C2919142 Short stature adverse event C1840335 Hypomelia mullerian duct anomalies OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0314657 Genetic predisposition HSDN C4042891 Sleep wake disorders C0019557 Hip fx HSDN C2919142 Short stature adverse event C0033835 Pseudopseudohypoparathyroidism MalaCards|HPO C0028738 Nystagmus C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO C0857305 Thrombocytopenia purpura C0030297 Pancreatic neoplasm HSDN C1971624 Appetite absent C0043395 Yellow fever DiseaseOntology|OrphaNet|MalaCards C0020455 Hypergammaglobulinemia C0023895 Liver diseases HSDN C1963093 Dizziness adverse event C0009395 Color perception HSDN C0152020 Atony stomach C1843852 Spinocerebellar ataxia with epilepsy HPO C3829611 Nausea frequency C0013514 Echinostomiasis DiseaseOntology C0004604 Pain back C2984291 Glioblastoma multiforme pathway HSDN C0037763 Spasm C0042830 Perception visual HSDN C0009676 Confusion state C0033968 Psychotherapeutic technique HSDN C0497406 Over weight C0243026 Sepsis HSDN C0240735 Personality change C0030567 Parkinson disease MalaCards C2919142 Short stature adverse event C3891452 Seckel syndrome 8 MalaCards C4084773 Bothered by weight gain C1135821 Mortality syndrome, spiking HSDN C0018772 Deafness C0042029 Urinary tract infection HSDN C0018681 Headache, cephalalgia C0393739 Episodic cluster headache UMLS C2024878 Cardiovascular surgery result: dyspnea C0013927 Embolism, amniotic fluid HSDN C0009460 Communication impairment C0524851 Neurodegenerative disorders HSDN C4084784 Diarrhea C0175816 Cold hemagglutinin disease MalaCards C0242936 Center pain C0003892 Neurogenic arthropathy HSDN C4084767 Bothered by vomiting C1961100 Erectile dysfunction adverse event HSDN C0042964 Anticipatory vomiting C0034885 Rectal neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0020550 Hyperthyroidism HSDN C0018784 Deafness sensorineural C0023676 Life style HSDN C3898969 Have been vomiting C0014170 Endometrial neoplasms HSDN C3163620 Hypotension adverse event C0032001 Pituitary apoplexy OrphaNet|MalaCards C2911645 Weight loss adverse event C0036117 Salmonella infections HSDN C0162298 Stiffness joints C0795895 Acd-mental retardation syndrome OrphaNet|MalaCards C0860603 Anxiety symptom C0751254 Creutzfeldt-jakob disease, familial MalaCards|HPO C4020887 Photodysphoria C4041558 Cone-rod synaptic disorder, congenital nonprogressive MalaCards C0349489 Fetal hypoxia C0012739 Disseminated intravascular coagulation HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1861172 Venous thromboembolism HSDN C2024893 Cardiovascular surgery result: fatigue C0012644 Animal disease models HSDN C0020673 Hypothermia (central) (local) C0043397 Yellow fever, jungle MalaCards C0036572 Convulsion C4015062 Combined oxidative phosphorylation deficiency 22 MalaCards|UMLS C0020538 Hbp C1306214 Acth-secreting pituitary adenoma HPO C1963091 Diarrhea adverse event C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C0026826 High muscle tone C0393593 Dystonia disorders HSDN C0013595 Eczematous dermatitis C0268579 Propionic acidemia HPO C0036572 Convulsion C1845861 Mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait HPO C4084802 Usual severity diarrhea C0027726 Nephrotic syndrome HSDN C0023015 Language handicap C0010823 Cytomegalovirus infections HSDN C4084767 Bothered by vomiting C0022822 Hunchback formed after birth HSDN C0030486 Extremity paralysis, lower C3827868 Tachycardia by ecg finding HSDN C4084768 Usual severity vomiting C0033871 Psychiatric status rating scales HSDN C3641756 Have diarrhea C0011884 Diabetic retinopathy HSDN C0003811 Cardiac rhythm disturbance C0340951 Erythrogenesis imperfecta MalaCards C0019079 Bloody sputum C0221018 Hereditary sideroblastic anemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033289 Family relationship, professional HSDN C0009398 Color vision defects C0033578 Prostatic neoplasms HSDN C0030552 Paralysis partial C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C1557397 Adverse event associated with pain C0039483 Giant cell arteritis HSDN C0271215 Blindness legal C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C0042798 Vision dim C1306068 After-cataract HSDN C0424755 Fever symptoms C0014078 Venezuelan equine encephalomyelitis DiseaseOntology|MalaCards C0018777 Deafness, conductive C1846421 Lathosterolosis MalaCards|HPO C2911645 Weight loss adverse event C1856243 Growth factors, combined defect of OrphaNet|MalaCards C0030193 Sense of pain C1519487 Squamous cell breast carcinoma, spindle cell variant UMLS C1963249 Tinnitus adverse event C0015302 External exotoses HSDN C2242996 Tingling C0812393 Cancer patients and suicide and depression HSDN C0027796 Neuralgias C0039145 Syringomyelia and syringobulbia HSDN C3665386 Abnormal vision C1836122 Sarcoidosis, early-onset MalaCards C0151740 Intracranial hypertension C1334698 Meningothelial cell neoplasm MalaCards C0015469 Facial paralysis C1850126 Osteopetrosis, mild autosomal recessive form MalaCards|HPO C2203646 Jaundice C0006663 Calcinosis HSDN C0011991 Loose stools C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0033377 Caudal displacement C2675875 Chromosome 2p16.1 p15 deletion syndrome OrphaNet|MalaCards C3463815 Feel fatigue C0019829 Hodgkin disease OrphaNet C0000737 Abdomen pain C2219717 Menstrual periods stopped for over 6 months HSDN C0008031 Pain chest C0031099 Periodontitis HSDN C0917816 Deficiency mental C1848864 Thoracic dysplasia-hydrocephalus syndrome OrphaNet|MalaCards C0151798 Liver necrosis C0007095 Carcinoid tumor MalaCards C1961131 Cough adverse event C0021361 Female infertility HSDN C0042928 Paralysis vocal cord C1956346 Coronary artery disease HSDN C0030193 Sense of pain C0269102 Endometrioma UMLS C0277959 Hair coarseness C0265252 Coffin-lowry syndrome MalaCards|HPO C4084774 Have weight loss C0032969 Pregnancy in diabetics HSDN C0040822 D tremors C1090821 Sepsis (invertebrate) HSDN C0518090 Frequency of pain question C0017547 Gigantism HSDN C1962976 Ventricular fibrillation adverse event C2748541 Brugada syndrome 5 MalaCards|HPO C2107732 Consistent heat intolerance C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards|HPO C0010200 Cough symptom C1266144 Pleuropulmonary blastoma UMLS C0242936 Center pain C0034072 Cor pulmonale HSDN C4085549 Dizziness C0035305 Retinal detachment HSDN C0023380 Lethargy C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C0009421 Comatose C0026266 Mitral valve insufficiency HSDN C0019521 Hiccoughs C0038353 Stomach distended HSDN C0013404 Respiratory difficulty C0020538 Hypertensive disease HSDN|UMLS C2030274 Heavy bleeding between periods C0206680 Mesothelioma, cystic OrphaNet|MalaCards C1961131 Cough adverse event C0085655 Polymyositis OrphaNet|MalaCards C0917801 Sleep disorder insomnia C1261128 Progeria-like syndrome MalaCards C0242936 Center pain C0037942 Spinal osteophytosis HSDN C1963090 Dehydration adverse event C0009714 Hepatic fibrosis, congenital HPO C0015230 Exanthem C0271269 Keratitis in exanthema UMLS C0009792 Consciousness disorder C0011849 Diabetes mellitus HSDN C1557397 Adverse event associated with pain C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C3898969 Have been vomiting C0041374 Tumor virus infections HSDN C0424755 Fever symptoms C0038354 Stomach diseases HSDN C0557874 Global developmental delay C0751666 Canavan disease, infantile OrphaNet|HPO|MalaCards C3178766 Nociceptive pain C0458219 Complex regional pain syndromes HSDN C0034124 Pupillary disorder C0018674 Head trauma HSDN C1963170 Hypothermia adverse event C0018802 Congestive heart failure HSDN C0013604 Edematous C0039590 Testicular neoplasms HSDN C0155552 Hearing loss mixed C0032268 Pneumocephalus HSDN C0016204 Fart C0012814 Colon nos diverticulitis HSDN C3539023 Pelvic pain increasing in frequency C0038478 Struma ovarii HSDN C0008031 Pain chest C0001175 Acquired immunodeficiency syndrome HSDN|UMLS C4084726 Distress cough C0002871 Anemia HSDN C4084784 Diarrhea C3714602 Staphylococcal toxic shock syndrome MalaCards C1963087 Constipation adverse event C3493776 Hypothyroidism, congenital, nongoitrous, 1 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0035302 Retinal artery occlusion HSDN C3146279 Coma C1258104 Diffuse scleroderma HSDN C0034933 Abnormal reflexes C0020649 Hypotension HSDN C0020538 Hbp C0001193 Apert syndrome OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C1527336 Sjogren's syndrome HSDN C0004134 Dyssynergia C2931746 Sulfocysteinuria HPO|UMLS C2919142 Short stature adverse event C1844862 Abruzzo erickson syndrome OrphaNet|HPO|MalaCards C0018989 Paresis of one side of body C0154694 Spastic hemiplegia UMLS C1963252 Tremor adverse event C0021368 Inflammation HSDN C1549543 Administration method - pain C0149678 Epstein-barr virus infections HSDN C2911647 Weight gain adverse event C0004442 Avoidance learning HSDN C0013604 Edematous C1852759 Papillorenal syndrome MalaCards|HPO C0038002 Spleen enlargement C1863728 Hemophagocytic lymphohistiocytosis, familial, 4 MalaCards|HPO C0036572 Convulsion C0020503 Hyperparathyroidism, secondary HSDN C0262384 Chest pain atypical C0027051 Myocardial infarction UMLS C0023012 Delay language C3150925 Spastic ataxia 4, autosomal recessive HPO C3887873 Hearing loss C0014038 Encephalitis HSDN C4084767 Bothered by vomiting C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0851578 Disorder sleep C0042029 Urinary tract infection HSDN C0522224 Palsied C2609414 Acute kidney injury HSDN C0162298 Stiffness joints C0268225 Aspartylglucosaminuria MalaCards|HPO C4084784 Diarrhea C0020758 Congenital ichthyosis HSDN C3898969 Have been vomiting C0010074 Coronary vessel anomalies HSDN C0002170 Alopecia disorders C0085859 Polyglandular type i autoimmune syndrome HPO C0020538 Hbp C4054549 Medullary cystic kidney disease type i MalaCards C3539896 Pelvic pain occurs with urination C0520720 Cyst nerve root HSDN C0024031 Back pain lower back C0017638 Glioma HSDN C4084784 Diarrhea C3489393 Hiatal hernia HSDN C3898969 Have been vomiting C0011616 Contact dermatitis HSDN C0085606 Urination urgency C0600040 Chronic interstitial cystitis OrphaNet C1963093 Dizziness adverse event C0009450 Disease caused by microorganism HSDN C0007642 Cellulitis nos C0011633 Dermatomyositis MalaCards C0015469 Facial paralysis C3541340 Pontine tegmental cap dysplasia MalaCards C0010520 Skin cyanosis C0521801 Pulmonary cyanosis UMLS C0235153 Sensory hallucination C0023241 Legionnaires' disease MalaCards C1963087 Constipation adverse event C0460137 Push down or depress HSDN C0917816 Deficiency mental C0587248 Costello syndrome (disorder) OrphaNet|HPO|MalaCards C1963184 Nystagmus adverse event C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C1963093 Dizziness adverse event C0035078 Kidney failure HSDN C1963087 Constipation adverse event C0036421 Systemic scleroderma HSDN C0424755 Fever symptoms C0854795 Resectable hepatic malignant neoplasm MalaCards C0022568 Inflammation corneal C0003076 Aniridia OrphaNet C0013362 Dysarthrias C1963138 Hypertension adverse event HSDN C0344428 Ventricular tachycardia by ecg finding C1832680 Cardiomyopathy, dilated, 1e MalaCards C0577979 Expectoration, frothy C1761609 Aspiration pneumonitis MalaCards C4084767 Bothered by vomiting C0220847 C hepatitis virus HSDN C0020672 Body temperature decreased C0042018 Urinary calculi HSDN C4085211 Pain distress question C0206504 Tympanic membrane perforation HSDN C3665346 Loss sight C1859773 Microphthalmia, syndromic 3 OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0027667 Cancer origin unknown HSDN C0018524 Hallucinate C0014055 Encephalitis, epidemic HSDN C1279888 Proteinuria of undiagnosed cause C1881674 Medical device emits smoke HSDN C0518090 Frequency of pain question C0037280 Skin diseases, parasitic HSDN C0001825 Agraphia C0752347 Lewy body disease HSDN C0018784 Deafness sensorineural C0023787 Lipodystrophy MalaCards C0008031 Pain chest C0002965 Angina, unstable UMLS C4085211 Pain distress question C1546533 Specimen source codes - abscess HSDN C0009421 Comatose C0006285 Bronchopneumonia HSDN C4084725 Usual severity cough C0018824 Heart valve disease HSDN C0042940 Disorder of voice C4085311 Depression - recess HSDN C2029884 Hearing loss by exam C0009375 Colonic neoplasms HSDN C0241210 Speaking delay C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C1549543 Administration method - pain C0038874 Supratentorial neoplasms HSDN C0039070 Collapse fleeting C0748350 Respiratory arrest without trauma UMLS C1961100 Erectile dysfunction adverse event C0268407 Senile cardiac amyloidosis MalaCards C4084724 Usual severity constipation C0011849 Diabetes mellitus HSDN C0009806 Constipate C0238015 Autonomic dysreflexia HSDN C0344315 Mood depressed C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C1963180 Neck pain adverse event C0018946 Hematoma, subdural HSDN C2364111 Gustatory anesthesia C0042594 Vestibular diseases HSDN C4085661 Usual severity nausea C1423541 Vangl2 gene HSDN C3812171 Bradycardia by ecg finding C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards|HPO C0033774 Skin pruritus C0040028 Thrombocythemia, essential MalaCards C1963281 Vomiting adverse event C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4084775 Usual severity weight loss C0016470 Food allergy HSDN C0013604 Edematous C0018889 Helminthiasis HSDN C0015468 Face pain C2911643 Encounter due to family history of osteoporosis HSDN C0030193 Sense of pain C1334743 Metastatic squamous cell breast carcinoma UMLS C0010200 Cough symptom C1334651 Choriocarcinoma of mediastinum UMLS C4084788 Have dizziness C0014511 Epithelial cyst HSDN C0004604 Pain back C0030286 Pancreatic diseases HSDN C2233627 Pigmented eyelid growth C0015424 Eyelid neoplasms UMLS C0002963 Angina variant C0032787 Postoperative complications HSDN C0042571 Vertigo subjective C0338078 Non-functioning pituitary gland neoplasm MalaCards C0151818 Opisthotonos C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO|UMLS C1557397 Adverse event associated with pain C1412004 Tumor of the pineal region HSDN C0038868 Supranuclear palsy progressive C0018799 Heart diseases HSDN C0003550 Broca aphasia C0033923 Psychomotor function HSDN C0013362 Dysarthrias C1527311 Brain edema HSDN C0011991 Loose stools C0024138 Lupus erythematosus, discoid HSDN C0000737 Abdomen pain C1336431 Ovarian embryonal carcinoma stage iv UMLS C4084774 Have weight loss C0024437 Macular degeneration HSDN C0557874 Global developmental delay C1956097 Wolf-hirschhorn syndrome OrphaNet|HPO|MalaCards C0848203 Male pelvic pain C1704436 Peripheral arterial diseases HSDN C1579931 Depressed - symptom C1834570 Myoclonic dystonia HPO C0036396 Sciatica C0006309 Brucellosis HSDN C0004134 Dyssynergia C1336537 Supratentorial meningioma MalaCards C0004093 Asthenia C0016751 Hereditary fructose intolerance syndrome HSDN C0015300 Ocular proptosis C1848488 Pierre robin syndrome with fetal chondrodysplasia OrphaNet|HPO C0018772 Deafness C2673873 Bardet-biedl syndrome 13 HPO C0020505 Excessive eating C0684274 Self regulation HSDN C0426579 Anorexia symptom C0001349 Acute-phase reaction HSDN C0015732 Feces incontinence C0270726 Alexander disease MalaCards C0007758 Cerebellar ataxia C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C1000483 Genus anemia C2673914 Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive MalaCards|HPO C0007859 Pain neck C0004935 Animal ethology HSDN C0010200 Cough symptom C0019693 Hiv infections HSDN C0030193 Sense of pain C0334573 Ameloblastic; fibrosarcoma UMLS C0035078 Failure kidney C0023195 Lecithin acyltransferase deficiency OrphaNet|HPO C0474500 Fecal discharge C0015732 Fecal incontinence UMLS C0018991 Paralysis one side of body C1145628 Autonomic nervous system disorders HSDN C0700590 Diaphoresis excessive C1721006 Keratoderma, palmoplantar, epidermolytic OrphaNet|HPO|MalaCards C0010200 Cough symptom C1334363 Large cell lung neuroendocrine carcinoma UMLS C3146279 Coma C0002989 Epithelioid hemangioma of skin HSDN C0002963 Angina variant C0001396 Stokes-adams syndrome HSDN C0518090 Frequency of pain question C0010074 Coronary vessel anomalies HSDN C0036572 Convulsion C0338479 Epilepsies, symptomatic myoclonic UMLS C0476273 Distress respiratory C3714582 Pneumonitis chemical MalaCards C0742303 Chest pain site left_sternal_border C0741025 Chest problem UMLS C0030193 Sense of pain C1333832 Favorable infiltrating breast carcinoma UMLS C3539895 Pelvic pain occurs with bowel movement C3178770 Nutcracker syndrome, renal HSDN C3641755 Have constipation C2984289 Melanoma pathway HSDN C0020796 Profoundly mentally retarded C2981150 Uranostaphyloschisis MalaCards C0007758 Cerebellar ataxia C0014481 Ephemeral fever HSDN C0016199 Pain flank C1306837 Papillary renal cell carcinoma UMLS C2984058 Have pain C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C4085661 Usual severity nausea C0013502 Echinococcosis HSDN C2242996 Tingling C0038436 Post-traumatic stress disorder HSDN C4084769 Vomiting frequency C0038661 Suicide HSDN C0018772 Deafness C0265253 Stickler syndrome (disorder) OrphaNet C1557397 Adverse event associated with pain C0036216 Sarcoma, experimental HSDN C0162834 Hyperpigmentation C0587248 Costello syndrome (disorder) MalaCards|HPO C0024282 Lymphocytosis C0220989 Acquired partial lipodystrophy OrphaNet|HPO|MalaCards C0013604 Edematous C0162568 Erythropoietic protoporphyria HPO C0332573 Macula C0265985 Mongolian spot UMLS C0424276 Repetitive dreams C0234458 Dream disorder UMLS C1549543 Administration method - pain C0039730 Thalassemia HSDN C0349588 Stature short C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) MalaCards C0031911 Pigment deposition C0346811 Malignant dermal neoplasm MalaCards C0020538 Hbp C0025427 Mercury poisoning OrphaNet|MalaCards C2242996 Tingling C1842534 Dystonia 18 (disorder) OrphaNet|HPO|MalaCards C4085211 Pain distress question C0033075 Presbyopia HSDN C0003862 Pain joint C1834340 Leigh syndrome, adult UMLS C0018784 Deafness sensorineural C0700095 Central neuroblastoma HSDN C0042940 Disorder of voice C0011548 Dependent personality disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0600518 Choroidal neovascularization HSDN C0851578 Disorder sleep C0751813 Chronic brain injury HSDN C0023012 Delay language C0221060 Mobius syndrome MalaCards C0016199 Pain flank C1336882 Infiltrating ureter urothelial carcinoma with squamous differentiation UMLS C1963087 Constipation adverse event C0034069 Pulmonary fibrosis HSDN C0085602 Polydypsia C0546817 Fluid overload UMLS C0454644 Delayed language development C0394006 Dysequilibrium syndrome HPO C4085641 Level of joint pain C1850568 Nakajo syndrome MalaCards C4084773 Bothered by weight gain C0344479 Spinal cord myelodysplasia HSDN C4084723 Constipation C1854630 Growth deficiency and mental retardation with facial dysmorphism MalaCards|HPO C4084724 Usual severity constipation C0238027 Botulism, infantile OrphaNet|MalaCards C4084769 Vomiting frequency C0016989 Galvanic skin response HSDN C3898969 Have been vomiting C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C4084897 Sleep disturbance subordinate domain C0162809 Kallmann syndrome HPO C0013362 Dysarthrias C3495554 Homocarnosinase deficiency MalaCards C0151686 Growth retardation C0268151 Classical galactosemia MalaCards C2984058 Have pain C0747533 Peroneal neuropathy HSDN C0522224 Palsied C1962986 Glaucoma adverse event HSDN C0002962 Angina C0008924 Cleft lip HSDN C0042024 Urine incontinence C0003850 Arteriosclerosis HSDN C1557397 Adverse event associated with pain C0029877 Ear inflammation HSDN C4084774 Have weight loss C0022758 Kap HSDN C4084784 Diarrhea C0040435 Tooth diseases HSDN C0042928 Paralysis vocal cord C0022408 Arthropathy HSDN C4084767 Bothered by vomiting C0015745 Ingestive behavior HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032987 Ectopic pregnancy HSDN C3665492 Pigmentations C0268495 Oculocutaneous albinism type 2 MalaCards C3665346 Loss sight C1839040 Leber optic atrophy and dystonia UMLS C0494475 Seizure generalized tonic clonic C4015395 Generalized epilepsy with febrile seizures plus, type 9 MalaCards C1557397 Adverse event associated with pain C0031347 Pharyngeal neoplasms HSDN C1384666 Decreased hearing C0020502 Hyperparathyroidism HSDN C3829611 Nausea frequency C0026865 Mushroom poisoning HSDN C0030193 Sense of pain C1705811 Terminology role entity HSDN C4084775 Usual severity weight loss C0007784 Cerebral hemisphere hemorrhage HSDN C4084723 Constipation C1550639 Specimen type - fistula HSDN C4084725 Usual severity cough C0007873 Uterine cervical neoplasm HSDN C0340288 Angina stable C0018128 Graft occlusion, vascular HSDN C4084802 Usual severity diarrhea C0206245 Amyloid neuropathies, familial MalaCards C4085661 Usual severity nausea C0022951 Lactose intolerance HSDN C0013595 Eczematous dermatitis C1531773 Currarino triad HPO C3463815 Feel fatigue C0039336 Gustatory sense HSDN C0349588 Stature short C3553582 Seckel syndrome 6 MalaCards C0026826 High muscle tone C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C2032396 Pelvic pain on the right C2706915 Language:-:point in time:^patient:- HSDN C0011991 Loose stools C0039590 Testicular neoplasms HSDN C0013421 Dystonia C1850100 Parkinson disease 15, autosomal recessive (disorder) HPO C0013144 Drowsy C0014061 Tick-borne encephalitis MalaCards C0030200 Intractable pain C0036341 Schizophrenia HSDN C4084784 Diarrhea C0010674 Cystic fibrosis HSDN C4084784 Diarrhea C0018852 Heavy chain disease HSDN C4085211 Pain distress question C0010074 Coronary vessel anomalies HSDN C0005745 Blepharoptosis C0175701 Aarskog syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0005119 Bereavement HSDN C0518090 Frequency of pain question C0041755 Adverse reaction to drug HSDN C0750937 Appendicular ataxia C1847725 Spinocerebellar ataxia 15 MalaCards C1950154 Insomnia homeopathic medication C0948264 Neuroborreliosis MalaCards C0030554 Abnormal sensation C0020621 Hypokalemia HSDN C0035078 Failure kidney C0343208 Essential mixed cryoglobulinemia OrphaNet|MalaCards C0036572 Convulsion C3809414 Cortical dysplasia, complex, with other brain malformations 3 MalaCards|UMLS C2242996 Tingling C0020598 Hypocalcemia HSDN C3539892 Pelvic pain in front C1000483 Genus anemia HSDN C0518090 Frequency of pain question C0376547 Aromatherapy HSDN C0018772 Deafness C1857339 Deafness, congenital, with vitiligo and achalasia MalaCards C1963180 Neck pain adverse event C0032319 Pneumopericardium HSDN C1145670 Failure respiratory C0265281 Metatropic dwarfism MalaCards|HPO C4084766 Vomiting C1000483 Genus anemia HSDN C0027796 Neuralgias C0453996 Tobacco smoking HSDN C2919142 Short stature adverse event C1859591 Aural atresia, multiple congenital anomalies, and mental retardation OrphaNet|MalaCards C3815497 Cough C0029342 Orthomyxoviridae infections HSDN C2024893 Cardiovascular surgery result: fatigue C1859726 Arterial tortuosity syndrome MalaCards C0746674 Muscle weakness generalized C0017921 Glycogen storage disease type ii OrphaNet|MalaCards C0004604 Pain back C0035222 Respiratory distress syndrome, adult HSDN C4084775 Usual severity weight loss C0020676 Hypothyroidism HSDN C4084727 Cough frequency C0007772 Intracranial arteriovenous malformation HSDN C0010200 Cough symptom C1619738 Immune reconstitution inflammatory syndrome HSDN C2203646 Jaundice C3714644 Thymus neoplasms HSDN C1260922 Respiratory abnormality C0268680 Biotin deficiency MalaCards C3665346 Loss sight C0043324 Juvenile xanthogranuloma MalaCards C0008031 Pain chest C0025286 Meningioma HSDN C0018681 Headache, cephalalgia C0346300 Pituitary carcinoma OrphaNet|MalaCards C0037763 Spasm C0004623 Bacterial infections HSDN C0004941 Behavioral symptoms C0087012 Ataxia, spinocerebellar MalaCards C0349588 Stature short C1415737 Hsd11b2 gene HPO C0004604 Pain back C0029928 Ovarian diseases HSDN C0013604 Edematous C0026691 Mucocutaneous lymph node syndrome OrphaNet|MalaCards C0024031 Back pain lower back C0752191 Central nervous system schistosomiasis HSDN C0020538 Hbp C0010308 Congenital hypothyroidism MalaCards C0036572 Convulsion C0079027 Blood loss, surgical HSDN C2919142 Short stature adverse event C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C4085661 Usual severity nausea C0014118 Endocarditis HSDN C3887784 Decreased urine output C0018802 Congestive heart failure HSDN C0751495 Seizure focal C1848137 Epilepsy, female-restricted, with mental retardation (disorder) MalaCards|HPO|UMLS C4084775 Usual severity weight loss C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0184567 Pain acute C2350572 Illness behavior HSDN C0007758 Cerebellar ataxia C0023470 Myeloid leukemia HSDN C0162835 Hypopigmentation C1859910 Albinism-microcephaly digital anomalies syndrome MalaCards C4084766 Vomiting C0456487 Peutz jeghers polyp MalaCards C0018777 Deafness, conductive C1837884 Larsen-like syndrome MalaCards C0040485 Wryneck C2231323 Left-sided ocular torticollis UMLS C4084776 Weight loss C0042995 Vulvar neoplasms HSDN C0221263 Cafe au lait spot C0795818 Chromosome 7 ring syndrome MalaCards C0004604 Pain back C0038579 Substance abuse, intravenous HSDN C4085211 Pain distress question C0024841 Matrimony, matrimonial HSDN C0522224 Palsied C0013990 Pathological accumulation of air in tissues HSDN C4085211 Pain distress question C0033575 Prostatic diseases HSDN C0004604 Pain back C0013394 Coitus painful HSDN C0030552 Paralysis partial C0085179 Eosinophilia-myalgia syndrome HSDN C3178766 Nociceptive pain C0030318 Panic state HSDN C0037771 Paraparesis spastic C0376549 Roseolovirus infections HSDN C0015672 Decreased energy C0264743 Rheumatic fever without heart involvement MalaCards C0008031 Pain chest C0016664 Fatigue fracture HSDN C0151786 Weakness muscle C0006147 Breast fed HSDN C4084775 Usual severity weight loss C0279607 Adult primary hepatocellular carcinoma MalaCards C0030552 Paralysis partial C1962979 Burn adverse event HSDN C0004134 Dyssynergia C0024141 Lupus erythematosus, systemic HSDN C3641755 Have constipation C0162565 Acute intermittent porphyria OrphaNet|HSDN|HPO|MalaCards C3541349 Syncope C0949570 Allergies wheat HSDN C0029163 Hemorrhage mouth C0398368 Lymphatic abnormalities HSDN C4084769 Vomiting frequency C0035361 Pneumoretroperitoneum HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0376545 Hematologic neoplasms HSDN C0151889 Reflexes tendon increased C2677590 Congenital disorder of glycosylation, type in MalaCards|HPO C0019572 Hairiness C0024433 Macrostomia HSDN C0242936 Center pain C0010635 Cystadenoma, mucinous HSDN C0040822 D tremors C0007137 Squamous cell carcinoma HSDN C0030193 Sense of pain C0036039 Sadism HSDN C4085210 Usual severity pain C0018915 Hemangioendothelioma HSDN C0024031 Back pain lower back C0262584 Carcinoma, small cell HSDN C0033377 Caudal displacement C2931092 Maternally inherited leigh syndrome MalaCards C0233565 Bradykinesia C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0917816 Deficiency mental C3889475 Bardet-biedl syndrome 19 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0042065 Genitourinary neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0033348 Language program HSDN C3274924 Have been coughing C0022107 Irritable mood HSDN C4042891 Sleep wake disorders C0042830 Perception visual HSDN C0008031 Pain chest C0039263 Takayasu arteritis OrphaNet|HSDN|HPO|MalaCards C0030794 Pelvis pain C1261473 Sarcoma HSDN C1971624 Appetite absent C0004576 Babesiosis MalaCards C1557397 Adverse event associated with pain C2350529 Pulmonary aspergillosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037369 Smoking HSDN C0023530 Leukopenia C1961835 Gaucher disease, type 1 MalaCards|HPO C0221184 Hemianopsia bitemporal C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C0004134 Dyssynergia C4015307 Perrault syndrome 5 MalaCards|UMLS C0000737 Abdomen pain C0010692 Cystitis HSDN C0851578 Disorder sleep C0037744 Perceptual spatial orientation HSDN C0013404 Respiratory difficulty C0039128 Syphilis HSDN C1963281 Vomiting adverse event C0042076 Urologic neoplasms HSDN C1384606 Dyspareunia C1334818 Multicystic mesothelioma of peritoneum MalaCards C0851578 Disorder sleep C0027743 Nerve compression syndrome HSDN C3641755 Have constipation C0036421 Systemic scleroderma HSDN C0012569 Double vision C0007820 Cerebrovascular disorders HSDN C3539892 Pelvic pain in front C0040136 Thyroid neoplasm HSDN C1963086 Confusion adverse event C0020258 Hydrocephalus, normal pressure HSDN C4084775 Usual severity weight loss C1963198 Pancreatitis adverse event HSDN C4084802 Usual severity diarrhea C1865145 Congenital disorder of glycosylation type 1b MalaCards|HPO C0022346 Yellow skin C1332246 Ampulla of vater clear cell adenocarcinoma UMLS C0151889 Reflexes tendon increased C1836632 Spastic paraplegia 26, autosomal recessive (disorder) MalaCards C0012833 Dizzy C0013364 Dysautonomia, familial HSDN C0040485 Wryneck C0151491 Congenital musculoskeletal anomalies HSDN C1963170 Hypothermia adverse event C0009953 Convulsive therapy HSDN C0004134 Dyssynergia C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0151686 Growth retardation C2936910 Cross-mckusick-breen syndrome OrphaNet|MalaCards C0003862 Pain joint C0155943 Arthralgia of temporomandibular joint UMLS C0008031 Pain chest C1334455 Pulmonary sclerosing hemangioma HSDN|UMLS C4084774 Have weight loss C0032533 Polymyalgia rheumatica MalaCards C4084784 Diarrhea C0009730 Spinal meningocele HSDN C0151786 Weakness muscle C0033348 Language program HSDN C1959630 Eye pain adverse event C1546533 Specimen source codes - abscess HSDN C0004134 Dyssynergia C0751783 Lafora disease HSDN C0424755 Fever symptoms C0041755 Adverse reaction to drug HSDN C4084725 Usual severity cough C0019080 Hemorrhage HSDN C4084774 Have weight loss C0030809 Pemphigus vulgaris OrphaNet|MalaCards C0003862 Pain joint C0010346 Crohn disease HSDN C0015469 Facial paralysis C0034067 Pulmonary emphysema HSDN C3539020 Pelvic pain decreasing in frequency C0005586 Bipolar disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0031350 Pharyngitis HSDN C0221166 Paraparesis C0162565 Acute intermittent porphyria MalaCards|HSDN|HPO C0002965 Crescendo angina C0022661 Kidney failure, chronic HSDN C1962972 Proteinuria adverse event C0039336 Gustatory sense HSDN C0042963 Symptoms vomiting C0019061 Hemolytic-uremic syndrome HSDN C0009806 Constipate C0011854 Diabetes mellitus, insulin-dependent HSDN C0013428 Painful urination C1512740 Infiltrating bladder urothelial carcinoma, microcystic variant UMLS C0032285 Pneum C0043194 Wiskott-aldrich syndrome MalaCards C0040822 D tremors C2984291 Glioblastoma multiforme pathway HSDN C0033774 Skin pruritus C0011630 Dermatomycoses HSDN C0013404 Respiratory difficulty C1963137 Hydrocephalus adverse event HSDN C2024878 Cardiovascular surgery result: dyspnea C0221757 Alpha 1-antitrypsin deficiency HPO C1962972 Proteinuria adverse event C0268226 Type i mucolipidosis HPO C0037317 Sleep disturbance C3150675 Chromosome 15q24 duplication syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0005689 Bladder exstrophy HSDN C1963281 Vomiting adverse event C1335398 Gastric peutz-jeghers polyp MalaCards C0020580 Decreased sensation C0015467 Neuralgia facial HSDN C0011991 Loose stools C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C4042891 Sleep wake disorders C0008626 Congenital chromosomal disease HSDN C0009398 Color vision defects C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0349588 Stature short C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C0033774 Skin pruritus C0546884 Hypovolemia HSDN C0042024 Urine incontinence C0268407 Senile cardiac amyloidosis MalaCards C0002962 Angina C0017181 Gastrointestinal hemorrhage HSDN C0234132 Pyramidal sign C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease OrphaNet|HPO C2237041 Shox gene with short stature C2751878 Hadziselimovic syndrome MalaCards C1384666 Decreased hearing C2940786 Thyroid hormone resistance syndrome HPO C0012833 Dizzy C0243026 Sepsis HSDN C0026821 Cramp C1546635 Specimen source codes - fistula HSDN C2024893 Cardiovascular surgery result: fatigue C2937358 Cerebral hemorrhage HSDN C3887873 Hearing loss C0243026 Sepsis HSDN C0011991 Loose stools C0042024 Urinary incontinence HSDN C0221752 Rbc urine C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0151786 Weakness muscle C3839212 Familial hyperaldosteronism type 2 MalaCards C4084802 Usual severity diarrhea C0005424 Biliary tract diseases HSDN C0242936 Center pain C0032310 Pneumonia, viral HSDN C0000727 Abdomen acute C0344315 Depressed mood HSDN C0029163 Hemorrhage mouth C0428953 Ecg infarction myocardial HSDN C1961131 Cough adverse event C0038187 Starvation HSDN C2024878 Cardiovascular surgery result: dyspnea C0005940 Bone diseases HSDN C4084776 Weight loss C0151744 Myocardial ischemia HSDN C0026826 High muscle tone C0011265 Presenile dementia MalaCards C4084784 Diarrhea C0027666 Neoplasms, radiation-induced HSDN C0036659 Sensation disorder C0020564 Hypertrophy HSDN C4084802 Usual severity diarrhea C0020544 Renal hypertension HSDN C0036659 Sensation disorder C1963138 Hypertension adverse event HSDN C1963167 Memory impairment adverse event C0282492 Sneddon syndrome OrphaNet|HPO|MalaCards C2242996 Tingling C0040409 Tongue diseases HSDN C0042571 Vertigo subjective C1636667 Disorder characterized by eosinophilia HSDN C0009806 Constipate C0080179 Vertebra fracture HSDN C0030552 Paralysis partial C0520679 Sleep apnea, obstructive HSDN C4084723 Constipation C0403447 Chronic kidney insufficiency HSDN C0007758 Cerebellar ataxia C1859598 Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia OrphaNet|HPO|MalaCards C0033790 Pseudobulbar palsy C0001726 Affective symptoms HSDN C3539892 Pelvic pain in front C0019065 Hemorrhage intraperitoneal HSDN C0033774 Skin pruritus C0036508 Seborrheic dermatitis DiseaseOntology C0005745 Blepharoptosis C0376524 Branchio-oculo-facial syndrome MalaCards|HPO C2911647 Weight gain adverse event C0007282 Carotid stenosis HSDN C0424755 Fever symptoms C1552527 Clinic / center - developmental disabilities HSDN C2911645 Weight loss adverse event C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C0002622 Amnesias C0021603 Sleep initiation and maintenance disorders HSDN C2984058 Have pain C0699744 Infection of ear HSDN C0031911 Pigment deposition C0004779 Basal cell nevus syndrome MalaCards C0013404 Respiratory difficulty C0037299 Skin ulcer HSDN C0015672 Decreased energy C0024228 Lymphatic diseases HSDN C0007758 Cerebellar ataxia C0007137 Squamous cell carcinoma HSDN C4084768 Usual severity vomiting C0026785 Munchhausen syndrome HSDN C0518090 Frequency of pain question C0206694 Mucoepidermoid carcinoma HSDN C0151786 Weakness muscle C0020473 Hyperlipidemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018923 Hemangiosarcoma HSDN C4084788 Have dizziness C0012691 Dislocations HSDN C4084766 Vomiting C0011253 Delusions HSDN C0242936 Center pain C0010633 Cystadenoma HSDN C2911647 Weight gain adverse event C0024530 Malaria HSDN C1557397 Adverse event associated with pain C0155490 Middle ear cholesteatoma HSDN C0349588 Stature short C1858079 Osteoarthritis with mild chondrodysplasia HPO C0851578 Disorder sleep C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards C2029884 Hearing loss by exam C0019372 Herpesviridae infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0004763 Barrett esophagus HSDN C0158194 Pain in joint, other specified sites C0810055 Other non-traumatic joint disorders UMLS C2984057 Have nausea C0005426 Biliary tract neoplasm HSDN C0018524 Hallucinate C0037286 Skin neoplasms HSDN C0004134 Dyssynergia C0087012 Ataxia, spinocerebellar MalaCards|UMLS C0030554 Abnormal sensation C0037313 Sleep HSDN C0030232 Color loss C0033893 Tension headache HSDN C4085211 Pain distress question C0016412 Folic acid deficiency HSDN C0013428 Painful urination C0034885 Rectal neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C2931878 Familial primary biliary cirrhosis MalaCards C4084774 Have weight loss C2981150 Uranostaphyloschisis HSDN C0009676 Confusion state C0021229 Individuation HSDN C1963137 Hydrocephalus adverse event C1857780 Joubert syndrome 5 MalaCards C0018989 Paresis of one side of body C3839866 Familial cerebral saccular aneurysm MalaCards C1145670 Failure respiratory C1834928 Cloverleaf skull micromelia thoracic dysplasia OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0037578 Soft tissue injury HSDN C0042024 Urine incontinence C1853710 Hereditary motor and sensory neuropathy, type iic (disorder) MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0019294 Hernia, inguinal HSDN C1999266 Depression adverse event C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0040485 Wryneck C2827407 Infectious otitis media HSDN C0013604 Edematous C0034067 Pulmonary emphysema HSDN C4084723 Constipation C0025467 Mesentery, cyst HSDN C0006370 Bulimia C0033944 Psychosexual development HSDN C0008031 Pain chest C1706377 Memory device component HSDN C3815497 Cough C0314657 Genetic predisposition HSDN C0034150 Skin purpura C0220704 Shprintzen syndrome MalaCards|HPO C0000737 Abdomen pain C2827407 Infectious otitis media HSDN C1549543 Administration method - pain C0043119 Werner syndrome HSDN C0033377 Caudal displacement C1850674 Minicore myopathy with external ophthalmoplegia (disorder) MalaCards|HPO C0043094 Weight gain C0343084 Capillary leak syndrome HSDN C0042024 Urine incontinence C0025500 Mesothelioma HSDN C0018681 Headache, cephalalgia C0477373 Other forms of migraine UMLS C0497406 Over weight C0026764 Multiple myeloma HSDN C0036572 Convulsion C0016952 Galactosemias MalaCards C1961131 Cough adverse event C0007121 Bronchogenic carcinoma HSDN C0018681 Headache, cephalalgia C1709153 Nasopharyngeal differentiated carcinoma UMLS C0012569 Double vision C0024198 Lyme disease HSDN C0151889 Reflexes tendon increased C0432371 Cocaine fetal syndrome OrphaNet|MalaCards C3641756 Have diarrhea C0086227 Enterobiasis HSDN C0003550 Broca aphasia C0004096 Asthma HSDN C1963071 Back pain adverse event C0009450 Disease caused by microorganism HSDN C0013428 Painful urination C3178970 Entrapment, pudendal nerve MalaCards C2984057 Have nausea C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0349506 Sun sensitivity C0220722 Cerebrooculofacioskeletal syndrome 1 OrphaNet|HPO C2237041 Shox gene with short stature C0265263 Femoral hypoplasia - unusual facies syndrome OrphaNet|MalaCards C0013456 Pain ear C0024689 Mandibular diseases HSDN C2107732 Consistent heat intolerance C2748568 Immune dysfunction with t-cell inactivation due to calcium entry defect 1 MalaCards|HPO C0302148 Blood clot C1865145 Congenital disorder of glycosylation type 1b MalaCards C0020578 Hyperventilate C1704272 Benign prostatic hyperplasia HSDN C3463815 Feel fatigue C0042345 Varicosity HSDN C0151798 Liver necrosis C0206624 Hepatoblastoma MalaCards C0003811 Cardiac rhythm disturbance C0265265 Aase syndrome MalaCards C0015469 Facial paralysis C0700594 Radiculopathy HSDN C4084775 Usual severity weight loss C0919691 Anastomotic leaks HSDN C0917816 Deficiency mental C0268233 Galactosialidosis OrphaNet|HPO|MalaCards C0575081 Abnormal gait C1853926 Nonaka myopathy MalaCards|HPO C1000483 Genus anemia C2676137 Diamond-blackfan anemia 1 MalaCards C0004604 Pain back C0206727 Nerve sheath tumors HSDN C0041834 Erythematous condition C0025267 Multiple endocrine neoplasia type 1 HPO C1961131 Cough adverse event C0717360 Disease lyme vaccine HSDN C0349588 Stature short C4053775 Pituitary stalk interruption syndrome MalaCards C4084802 Usual severity diarrhea C0000786 Spontaneous abortion HSDN C1384666 Decreased hearing C0009363 Congenital ocular coloboma (disorder) HSDN C4084802 Usual severity diarrhea C0017689 Glucagonoma OrphaNet|MalaCards C4085862 Bothered by nausea C0015328 Behavior, exploratory HSDN C4050613 Anxiety C1849157 Insulin-like growth factor i, resistance to MalaCards|HPO C0002965 Crescendo angina C0022660 Kidney failure, acute HSDN C0030794 Pelvis pain C0029400 Osteitis HSDN C0745813 Lower extremity cramp exertional C0740728 Lower extremity problem UMLS C4084897 Sleep disturbance subordinate domain C0220756 Niemann-pick disease, type c OrphaNet C0013604 Edematous C0033054 Prenatal exposure delayed effects HSDN C4085661 Usual severity nausea C0033578 Prostatic neoplasms HSDN C2919142 Short stature adverse event C0342200 Endemic cretinism MalaCards C0557874 Global developmental delay C0393559 Troyer syndrome HPO C0018775 Hearing loss bilateral C0032453 Polychondritis, relapsing HSDN C0242936 Center pain C0014549 Tonic-clonic epilepsy HSDN C0557874 Global developmental delay C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C1557397 Adverse event associated with pain C0030215 Palate tumor HSDN C1963071 Back pain adverse event C0023676 Life style HSDN C0349588 Stature short C1563705 Nephrogenic diabetes insipidus, type i HPO C2984058 Have pain C0023860 Listeriosis HSDN C4084775 Usual severity weight loss C0003869 Arthritis, infectious HSDN C1963252 Tremor adverse event C0023890 Liver cirrhosis HSDN C4084775 Usual severity weight loss C1548483 Leishmaniasis vaccine HSDN C0151786 Weakness muscle C0035372 Rett syndrome MalaCards|HPO C0917816 Deficiency mental C1859567 Bardet-biedl syndrome 9 MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0035309 Retinal diseases HSDN C0039070 Collapse fleeting C0001580 Adolescent behavior HSDN C0034150 Skin purpura C0036946 Sheep--diseases HSDN C0040822 D tremors C0030305 Pancreatitis HSDN C0030552 Paralysis partial C0030567 Parkinson disease HSDN C0037384 Snore C0018799 Heart diseases HSDN C0497406 Over weight C2706915 Language:-:point in time:^patient:- HSDN C0242936 Center pain C0040799 Traumatic subcutaneous emphysema HSDN C0018784 Deafness sensorineural C3888013 Hypnoses HSDN C1962957 Flushing adverse event C0001624 Adrenal gland neoplasms HSDN C0037763 Spasm C0009946 Conversion disorder HSDN C4085210 Usual severity pain C0035592 Infection, rickettsiaceae HSDN C1963249 Tinnitus adverse event C0038454 Cerebrovascular accident HSDN C0027796 Neuralgias C0038160 Staphylococcal infections HSDN C4084768 Usual severity vomiting C0036118 Salmonella infections, animal HSDN C0016382 Cutaneous vascular engorgement C1842839 Hypotrichosis 6 MalaCards|HPO C0151786 Weakness muscle C0011334 Dental caries HSDN C1962972 Proteinuria adverse event C0085136 Central nervous system neoplasms HSDN C3641756 Have diarrhea C0038579 Substance abuse, intravenous HSDN C4084775 Usual severity weight loss C0020295 Hydronephrosis HSDN C3887873 Hearing loss C3280402 Sclerosteosis 2 MalaCards C0241165 Skin thickening C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO|UMLS C0020673 Hypothermia (central) (local) C0041327 Tuberculosis, pulmonary HSDN C4085661 Usual severity nausea C1263846 Attention deficit hyperactivity disorder HSDN C0005745 Blepharoptosis C0028326 Noonan syndrome OrphaNet|HPO|MalaCards C0013421 Dystonia C0238286 Mucolipidosis type iv MalaCards|HPO C0009806 Constipate C0020517 Hypersensitivity HSDN C2984058 Have pain C0007774 Cerebral arterial diseases HSDN C1000483 Genus anemia C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C0018681 Headache, cephalalgia C0950123 Inborn genetic disease HSDN C2911647 Weight gain adverse event C0018965 Hematuria HSDN C1959630 Eye pain adverse event C0026961 Mydriasis HSDN C0018784 Deafness sensorineural C1849157 Insulin-like growth factor i, resistance to MalaCards C0151786 Weakness muscle C0270726 Alexander disease MalaCards C0002965 Crescendo angina C0008149 Chlamydia infections HSDN C0018681 Headache, cephalalgia C0233315 Premature birth of newborn HSDN C0851578 Disorder sleep C0023895 Liver diseases HSDN C0020673 Hypothermia (central) (local) C0006277 Bronchitis HSDN C0009806 Constipate C0861461 Colon nos cancer metastatic UMLS C0018777 Deafness, conductive C0812437 Oculo-dento-digital syndrome OrphaNet|HPO|MalaCards C4084784 Diarrhea C0033860 Psoriasis HSDN C1549543 Administration method - pain C0008523 Neoplasm choroid HSDN C4049644 Depression C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0004134 Dyssynergia C0042487 Venous thrombosis HSDN C0917816 Deficiency mental C1855089 Microcephalic primordial dwarfism, toriello type OrphaNet|MalaCards C1963137 Hydrocephalus adverse event C0340427 Familial dilated cardiomyopathy MalaCards C2237041 Shox gene with short stature C3278147 Geleophysic dysplasia 1 MalaCards C2911647 Weight gain adverse event C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C0557874 Global developmental delay C1956147 Microlissencephaly MalaCards C1549543 Administration method - pain C3536741 Discordant ventriculoarterial connection HSDN C4049644 Depression C1864851 Pigmented nodular adrenocortical disease, primary, 2 HPO C2919142 Short stature adverse event C1866504 Photosensitive trichothiodystrophy MalaCards|HPO C3146279 Coma C0428977 Bradycardia HSDN C0011991 Loose stools C0015230 Exanthema HSDN C0018772 Deafness C0029089 Ophthalmoplegia MalaCards C0036572 Convulsion C0376329 New variant creutzfeldt-jakob disease MalaCards C0036572 Convulsion C0040427 Tooth abnormalities HSDN C0036572 Convulsion C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO|UMLS C0035229 Respiratory function impaired C0206138 Crest syndrome MalaCards C0027796 Neuralgias C0597109 Nurse's role HSDN C1557397 Adverse event associated with pain C0008513 Chorioretinitis HSDN C4084767 Bothered by vomiting C0036875 Disorders of sex development HSDN C0013456 Pain ear C0270629 Epidural abscess HSDN C0557874 Global developmental delay C2932714 Pontocerebellar hypoplasia type 2 MalaCards C1963065 Apnea adverse event C0020255 Hydrocephalus HSDN C0042571 Vertigo subjective C0002438 Amebiasis HSDN C0030554 Abnormal sensation C0027073 Myofascial pain syndromes HSDN C1963281 Vomiting adverse event C0014457 Eosinophilia HSDN C3887873 Hearing loss C0018213 Graves disease HSDN C2984058 Have pain C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0026771 Trauma multiple HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027149 Myxoma HSDN C2911647 Weight gain adverse event C0029882 Otitis media HSDN C0015230 Exanthem C0085253 Adult-onset still disease OrphaNet|MalaCards C0020615 Hypoglycemia nos C1849157 Insulin-like growth factor i, resistance to MalaCards C0522224 Palsied C0022665 Kidney neoplasm HSDN C1549543 Administration method - pain C1691228 Cystic kidney diseases HSDN C4085210 Usual severity pain C0040592 Trachoma HSDN C0003862 Pain joint C0342881 Familial hypercholesterolemia - homozygous MalaCards|HPO C0008031 Pain chest C1555914 Psychologist - psychotherapy, group HSDN C1557397 Adverse event associated with pain C0003492 Aortic coarctation HSDN C0042024 Urine incontinence C0700327 Clinical findings relating to memory HSDN C0037763 Spasm C3814778 Hemolytic index HSDN C0700078 Deep tendon reflex decrease C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C0015230 Exanthem C3179349 Gastrointestinal stromal sarcoma MalaCards|HPO C4084784 Diarrhea C0008066 Child behavior disorders HSDN C0917816 Deficiency mental C0796068 Oculodigitoesophagoduodenal syndrome OrphaNet|HPO C0018780 Frequencies hearing high loss C0017416 Genital neoplasms, female HSDN C3274924 Have been coughing C0024232 Lymphatic metastasis HSDN C0426579 Anorexia symptom C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C4085549 Dizziness C0008350 Cholelithiasis HSDN C0009421 Comatose C0010346 Crohn disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0206255 Malaria vaccine HSDN C1069915 Vertigo C0019080 Hemorrhage HSDN C0042024 Urine incontinence C0011875 Diabetic angiopathies HSDN C0013404 Respiratory difficulty C0002792 Anaphylaxis HSDN C0151786 Weakness muscle C0079299 Epidermolysis bullosa simplex kobner OrphaNet C0242936 Center pain C0017510 Gestures HSDN C0011991 Loose stools C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C0030794 Pelvis pain C1519915 Vaginal adenosquamous carcinoma UMLS C4084802 Usual severity diarrhea C1548484 Rheumatic fever vaccine HSDN C2919142 Short stature adverse event C2931902 Acute brachial neuritis MalaCards C0040485 Wryneck C0001430 Adenoma HSDN C1546759 Specimen source codes - pustule C1858361 Pyogenic arthritis, pyoderma gangrenosum and acne OrphaNet|HPO|MalaCards C0030193 Sense of pain C1336522 Adenoid cystic carcinoma of submandibular gland UMLS C0013604 Edematous C0042900 Vitiligo HSDN C0042798 Vision dim C0016658 Fracture bone HSDN C0042963 Symptoms vomiting C0013364 Dysautonomia, familial HPO C0013404 Respiratory difficulty C1963084 Colitis adverse event HSDN C0040034 Thrombocytopenia C2717750 Platelet alpha-granule deficiency MalaCards C0231341 Aging premature C0038368 Stomatognathic diseases HSDN C1384666 Decreased hearing C0002895 Anemia, sickle cell HSDN C3539896 Pelvic pain occurs with urination C0002989 Epithelioid hemangioma of skin HSDN C0851578 Disorder sleep C0041107 Trisomy HSDN C2315100 Pediatric failure to thrive C3281084 Congenital disorder of glycosylation, type ir MalaCards C0030552 Paralysis partial C0008519 Ectopic tissue HSDN C3887638 Failure to thrive in infant C0002892 Anemia, pernicious HSDN C3898969 Have been vomiting C2937225 Biotin deficiency disease MalaCards C0086565 Liver function abnormal C2750442 Hypermanganesemia with dystonia polycythemia and cirrhosis HPO C0033377 Caudal displacement C1843852 Spinocerebellar ataxia with epilepsy HPO C3887873 Hearing loss C0020443 Hypercholesterolemia HSDN C0027796 Neuralgias C0032987 Ectopic pregnancy HSDN C0021359 Infertility C0346303 Thyrotroph adenoma MalaCards C0016382 Cutaneous vascular engorgement C0011993 Vipoma OrphaNet|HSDN|MalaCards C4084769 Vomiting frequency C0521585 Gastrointestinal mucositis HSDN C3829611 Nausea frequency C0001173 Adult pyloric stenosis HSDN C0011991 Loose stools C0037299 Skin ulcer HSDN C0018681 Headache, cephalalgia C3897070 Childhood gliomatosis cerebri UMLS C4084723 Constipation C0002792 Anaphylaxis HSDN C2237041 Shox gene with short stature C3809686 Mental retardation, autosomal dominant 21 MalaCards C0030552 Paralysis partial C2936331 Sarcoglycanopathies HSDN C0518090 Frequency of pain question C0020514 Hyperprolactinemia HSDN C0151786 Weakness muscle C0010823 Cytomegalovirus infections HSDN C4085211 Pain distress question C0014457 Eosinophilia HSDN C0027497 Queasy C0860603 Anxiety symptoms HSDN C4084774 Have weight loss C0079731 B-cell lymphomas HSDN C0019572 Hairiness C0025517 Metabolic diseases HSDN C0020903 Illusion C1548578 Location characteristic id - smoking HSDN C0007166 Cardiac output decreased C1000483 Genus anemia HSDN C1510417 Apraxia of gait C0344479 Spinal cord myelodysplasia HSDN C1963071 Back pain adverse event C0001430 Adenoma HSDN C3829611 Nausea frequency C0035242 Respiratory tract diseases HSDN C4085548 Usual severity dizziness C0021400 Influenza HSDN C0700590 Diaphoresis excessive C3809006 Cardiofaciocutaneous syndrome 3 MalaCards C0151786 Weakness muscle C0023467 Leukemia, myelocytic, acute HSDN C4084724 Usual severity constipation C0026850 Muscular dystrophy HSDN C4084726 Distress cough C0036690 Septicemia HSDN C0085636 Light sensitivity C1839564 Jensen syndrome MalaCards C0013390 Cramps menstrual C0021368 Inflammation HSDN C4084776 Weight loss C0920350 Autoimmune thyroiditis HSDN C0003469 Anxiety disorder C3266101 22q11 partial monosomy syndrome HPO C4084724 Usual severity constipation C2911643 Encounter due to family history of osteoporosis HSDN C0036572 Convulsion C0085220 Cerebral amyloid angiopathy HSDN C2024893 Cardiovascular surgery result: fatigue C0027073 Myofascial pain syndromes HSDN C0018772 Deafness C0023895 Liver diseases HSDN C0036659 Sensation disorder C4050613 Anxiety scale (basc-2) HSDN C4084802 Usual severity diarrhea C0042164 Uveitis HSDN C3887638 Failure to thrive in infant C0175683 Citrullinemia HPO C0018777 Deafness, conductive C0038940 Surgical wound dehiscence HSDN C0010200 Cough symptom C0036946 Sheep--diseases HSDN C3665492 Pigmentations C1266114 Meningeal melanomatosis MalaCards C0518090 Frequency of pain question C0004775 Bartter disease HSDN C0042024 Urine incontinence C3244301 Coverage level - family HSDN C1263846 Attention deficit disorder with hyperactivity C0220769 Fg syndrome MalaCards|HPO C3641756 Have diarrhea C0007117 Basal cell carcinoma HSDN C2919142 Short stature adverse event C1851710 Lateral meningocele syndrome MalaCards|HPO C4084725 Usual severity cough C0011853 Diabetes mellitus, experimental HSDN C0030193 Sense of pain C0007772 Intracranial arteriovenous malformation HSDN C0011991 Loose stools C0079744 Diffuse large b-cell lymphoma HSDN C4084773 Bothered by weight gain C0343084 Capillary leak syndrome HSDN C4084802 Usual severity diarrhea C0016154 Fish disease HSDN C0040264 Ear ringing sound C0029463 Osteosarcoma HSDN C0043144 Wheeze C0264408 Childhood asthma UMLS C0015676 Mental fatigue C0024121 Lung neoplasms HSDN C1557397 Adverse event associated with pain C0041408 Turner syndrome HSDN C1557397 Adverse event associated with pain C0036412 Sclera HSDN C0043094 Weight gain C0008370 Cholestasis HSDN C2203646 Jaundice C0004045 Asphyxia neonatorum HSDN C0221263 Cafe au lait spot C0018273 Growth disorders HSDN C3463815 Feel fatigue C0018799 Heart diseases HSDN C0028738 Nystagmus C3150675 Chromosome 15q24 duplication syndrome HPO C4042891 Sleep wake disorders C0027661 Neoplasms, hormone-dependent HSDN C4084784 Diarrhea C1863236 Scid due to ada deficiency, early-onset HPO C0015672 Decreased energy C0041582 Ulcer HSDN C0151686 Growth retardation C0342646 Vitamin d-dependent rickets, type 2a HPO C0018524 Hallucinate C0004415 Aversion therapy HSDN C0518090 Frequency of pain question C0272375 Antithrombin iii deficiency HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016995 Gambling HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030807 Pemphigus, nos HSDN C2984057 Have nausea C0036240 Response, satiety HSDN C4020887 Photodysphoria C1850281 Optic atrophy 6 (disorder) MalaCards C1963252 Tremor adverse event C2677299 Cerebroretinal microangiopathy with calcifications and cysts (disorder) HPO C4084767 Bothered by vomiting C0010054 Coronary arteriosclerosis HSDN C0085602 Polydypsia C0030521 Parathyroid neoplasms MalaCards|HSDN C0851578 Disorder sleep C0018801 Heart failure HSDN C3641756 Have diarrhea C0030846 Penile diseases HSDN C0036572 Convulsion C0019621 Histiocytosis, langerhans-cell HSDN C0010038 Corneal opacity disorder C0033800 Pseudoglioma MalaCards C0233794 Memory impaired C1096902 Infantile sialic acid storage disease MalaCards C4084802 Usual severity diarrhea C0002940 Aneurysm HSDN C3898969 Have been vomiting C0001175 Acquired immunodeficiency syndrome HSDN C4085211 Pain distress question C0020217 Hydatidiform mole HSDN C4084724 Usual severity constipation C0162871 Aortic aneurysm, abdominal HSDN C0042024 Urine incontinence C0011570 Mental depression HSDN C2911645 Weight loss adverse event C0041948 Uremia HSDN C0042963 Symptoms vomiting C0036946 Sheep--diseases HSDN C0024031 Back pain lower back C0035455 Rhinitis HSDN C4085548 Usual severity dizziness C0004623 Bacterial infections HSDN C0012569 Double vision C0009946 Conversion disorder HSDN C0009806 Constipate C0010308 Congenital hypothyroidism OrphaNet|MalaCards C0010520 Skin cyanosis C0007177 Cardiac tamponade HSDN C0497406 Over weight C0029410 Osteoarthritis of hip HSDN C4085642 Level of joint stiffness C0220662 Arthrogryposis, distal, type 1 OrphaNet|HPO C0008031 Pain chest C0453996 Tobacco smoking HSDN C2233555 Epistaxis stops with manual pressure C0014591 Epistaxis UMLS C0751900 Motor tic C0795888 Autism, susceptibility to, x-linked 4 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0206654 Leiomyomatosis HSDN C0151686 Growth retardation C1850626 Nathalie syndrome MalaCards C1963167 Memory impairment adverse event C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C4085317 Diarrhea frequency C0085435 Arthritis, reactive OrphaNet|MalaCards C0557874 Global developmental delay C2675857 Holoprosencephaly 10 MalaCards C0232466 Feeding difficulty C2677590 Congenital disorder of glycosylation, type in OrphaNet|HPO|MalaCards C1963063 Anorexia adverse event C0037369 Smoking HSDN C2700617 Irritation - emotion C1563706 Nephrogenic diabetes insipidus, type ii HPO C0009421 Comatose C0003850 Arteriosclerosis HSDN C0000737 Abdomen pain C0206654 Leiomyomatosis HSDN C0751901 Tics vocal C0040517 Gilles de la tourette syndrome MalaCards|HPO C3898969 Have been vomiting C0022423 Judgement HSDN C0013421 Dystonia C1556682 Adverse event associated with infection HSDN C4084723 Constipation C0018099 Gout HSDN C3539889 Pelvic pain increasing in severity C0282606 Myomatous neoplasm HSDN C4084725 Usual severity cough C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C4085862 Bothered by nausea C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0020578 Hyperventilate C0019829 Hodgkin disease HSDN C0024902 Mastodynia C0017668 Focal glomerulosclerosis HSDN C1557397 Adverse event associated with pain C2939156 Development of sexuality HSDN C0031911 Pigment deposition C2931390 Anophthalmia, cleft lip-palate, facial anomalies, and cns anomalies and hypothalamic disorder MalaCards C4084897 Sleep disturbance subordinate domain C4015283 Mental retardation, autosomal recessive 46 MalaCards C0042928 Paralysis vocal cord C0006281 Congenital bronchogenic cyst HSDN C0018772 Deafness C0796016 Microphthalmia, syndromic 1 MalaCards|HPO C0016204 Fart C1458155 Mammary neoplasms HSDN C1145670 Failure respiratory C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C0522224 Palsied C0003962 Ascites HSDN C0030193 Sense of pain C0031526 Philadelphia chromosome HSDN C0018784 Deafness sensorineural C0007097 Carcinomas HSDN C4084774 Have weight loss C0018790 Cardiac arrest HSDN C0042964 Anticipatory vomiting C0024958 Maxillary sinus neoplasms HSDN C2911645 Weight loss adverse event C0268151 Classical galactosemia OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0042514 Tachycardia, ventricular HSDN C0751837 Gait ataxic C1969645 Ataxia, spastic, 3, autosomal recessive MalaCards|HPO|UMLS C1961131 Cough adverse event C0008924 Cleft lip HSDN C0015230 Exanthem C0406344 Ichthyosis follicular UMLS C0034150 Skin purpura C2937358 Cerebral hemorrhage HSDN C4049602 Hyperactivity C3809753 Mental retardation, autosomal recessive 38 MalaCards C0012833 Dizzy C0700327 Clinical findings relating to memory HSDN C0030193 Sense of pain C0025048 Meconium aspiration syndrome HSDN C1384666 Decreased hearing C2931280 Congenital alopecia, psychomotor retardation, convulsions OrphaNet|HPO|MalaCards C0241165 Skin thickening C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0151786 Weakness muscle C0004933 Behavior modification technique HSDN C0020578 Hyperventilate C0038454 Cerebrovascular accident HSDN C2984058 Have pain C0002736 Amyotrophic lateral sclerosis OrphaNet|HSDN|HPO|MalaCards C4085661 Usual severity nausea C0037937 Spine injury HSDN C4085317 Diarrhea frequency C0027813 Neuritis HSDN C3887638 Failure to thrive in infant C1865372 Athabaskan severe combined immunodeficiency HPO C0557874 Global developmental delay C3541340 Pontine tegmental cap dysplasia MalaCards C2096293 Ent surgical result ear vertigo C0043253 Trauma blunt HSDN C0036396 Sciatica C0003467 Anxiety HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0595812 Fistula route HSDN C0241237 Standing difficulty C1838657 Vitamin d hydroxylation-deficient rickets, type 1b HPO|UMLS C0018932 Bright red rectal bleeding C0086768 Pancreatic cholera MalaCards C0426579 Anorexia symptom C1963064 Anxiety adverse event HSDN C0003862 Pain joint C0009375 Colonic neoplasms HSDN C2203646 Jaundice C0038395 Streptococcal infections HSDN C0848203 Male pelvic pain C1394494 Cystocele, unspecified HSDN C0009806 Constipate C0279639 Mucinous adenocarcinoma of the colon UMLS C4084775 Usual severity weight loss C1567741 Alport syndrome OrphaNet C0026838 Spasticity muscle C0015464 Facial nerve diseases HSDN C0012833 Dizzy C0015467 Neuralgia facial HSDN C3274924 Have been coughing C2240378 Cleft palate on exam HSDN C0036572 Convulsion C0019054 Hemolysis (disorder) HSDN C0162835 Hypopigmentation C0795949 Galloway mowat syndrome HPO C4084768 Usual severity vomiting C0016053 Fibromyalgia HSDN C0522224 Palsied C0020545 Hypertension, renovascular HSDN C0085631 Abnormal excitement C0242188 Spider bites HSDN C0022346 Yellow skin C0002876 Congenital dyserythropoietic anemia HSDN C4085661 Usual severity nausea C0025427 Mercury poisoning OrphaNet|MalaCards C4085548 Usual severity dizziness C4085311 Depression - recess HSDN C0013428 Painful urination C0279681 Bladder squamous cell carcinoma UMLS C4085211 Pain distress question C0037315 Sleep apnea syndromes HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030790 Pelvis infection HSDN C2984058 Have pain C3536741 Discordant ventriculoarterial connection HSDN C4084769 Vomiting frequency C0029835 Other specified tularemia nos DiseaseOntology|MalaCards C0022346 Yellow skin C1849387 Rh-null, regulator type HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C0023012 Delay language C1836929 Emanuel syndrome OrphaNet|MalaCards C2984057 Have nausea C1705812 Nci thesaurus role HSDN C0917816 Deficiency mental C2720434 Macroencephaly OrphaNet|MalaCards C0000737 Abdomen pain C0343206 Hypocomplementemic urticarial vasculitis MalaCards C2919142 Short stature adverse event C2675746 Craniodiaphyseal dysplasia, autosomal dominant (disorder) HPO C3887873 Hearing loss C0029125 Optic atrophies, hereditary HSDN C0015469 Facial paralysis C0344434 Atrial fibrillation ecg HSDN C0037317 Sleep disturbance C3280887 Hyperglycinemia, lactic acidosis, and seizures UMLS C3641756 Have diarrhea C2117118 X-ray of toe: deformity contracture HSDN C3274924 Have been coughing C0403447 Chronic kidney insufficiency HSDN C0028738 Nystagmus C3888209 Spastic paraplegia 45, autosomal recessive MalaCards C0013604 Edematous C0007131 Non-small cell lung carcinoma HSDN C1963184 Nystagmus adverse event C1837713 Joubert syndrome 3 MalaCards|HPO C0028961 Urine output decreased C0019151 Hepatic encephalopathy HSDN C0086565 Liver function abnormal C3809592 Mitochondrial dna depletion syndrome 13 (encephalomyopathic type) MalaCards C0016199 Pain flank C1720894 Genitourinary disease, male HSDN C0086439 Activity decreased C0425045 Sudden infant death HSDN C3463815 Feel fatigue C0033785 Pseudarthrosis HSDN C2237041 Shox gene with short stature C0497327 Dementia MalaCards C4084773 Bothered by weight gain C1269683 Major depressive disorder HSDN C4085211 Pain distress question C0041325 Peritonitis, tuberculous MalaCards|HSDN C0557874 Global developmental delay C2930900 Beta-sarcoglycanopathy MalaCards C0030193 Sense of pain C0015670 Child father HSDN C0011991 Loose stools C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C0038506 Stutter C1552527 Clinic / center - developmental disabilities HSDN C4085317 Diarrhea frequency C0023869 Lithiasis HSDN C4085661 Usual severity nausea C0595812 Fistula route HSDN C4084767 Bothered by vomiting C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C2911647 Weight gain adverse event C0042384 Vasculitis HSDN C2032434 Pain in right temporomandibular joint C0039496 Temporomandibular joint dysfunction syndrome UMLS C0028738 Nystagmus C1837541 Spinocerebellar ataxia 20 MalaCards C0030552 Paralysis partial C0019699 Hiv seropositivity HSDN C0042571 Vertigo subjective C0042170 Uveomeningoencephalitic syndrome HSDN C0015672 Decreased energy C1864851 Pigmented nodular adrenocortical disease, primary, 2 MalaCards C0851578 Disorder sleep C0014548 Epilepsy, generalized HSDN C0026826 High muscle tone C0751882 Myasthenic syndromes, congenital HSDN C0013604 Edematous C0012813 Diverticulitis HSDN C1557397 Adverse event associated with pain C0022078 Iris diseases HSDN C0242936 Center pain C0080032 Pleural effusion, malignant HSDN C0349588 Stature short C1862471 Arthrogryposis, distal, type 6 OrphaNet|MalaCards C4084724 Usual severity constipation C0005416 Biliary dyskinesia HSDN C0085593 Chill C0276108 Chlamydia infection psittaci MalaCards C0022346 Yellow skin C1868679 Griscelli syndrome, type 2 OrphaNet|HPO|MalaCards C0476273 Distress respiratory C1535939 Pneumocystis jiroveci pneumonia UMLS C0234132 Pyramidal sign C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|UMLS C0042963 Symptoms vomiting C0017155 Gastritis, hypertrophic HSDN C3829611 Nausea frequency C0004933 Behavior modification technique HSDN C4085210 Usual severity pain C0024862 Masochism HSDN C4084769 Vomiting frequency C1522136 Hypernatremia result HSDN C1279888 Proteinuria of undiagnosed cause C0004626 Pneumonia, bacterial HSDN C0018991 Paralysis one side of body C0037769 West syndrome HSDN C2024878 Cardiovascular surgery result: dyspnea C0021390 Inflammatory bowel diseases HSDN C0018681 Headache, cephalalgia C0314657 Genetic predisposition HSDN C4084802 Usual severity diarrhea C0156147 Crohn's disease of large bowel MalaCards C4085222 Nausea C0011849 Diabetes mellitus HSDN C0018834 Brash C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C0020580 Decreased sensation C0030846 Penile diseases HSDN C0878773 Bladder hyperactive C0018802 Congestive heart failure HSDN C1850534 Generalized edema C1859753 Acc with intestinal lymphangiectasia MalaCards C0028738 Nystagmus C0796147 Acrocallosal syndrome MalaCards|HPO C1549543 Administration method - pain C1868649 Panic disorder 1 HSDN C2052800 Penile reddening C0220620 Gastrointestinal carcinoid tumor MalaCards C0577567 Mass of urogenital structure C0341683 Echinococcosis kidney UMLS C4084775 Usual severity weight loss C0007682 Cns disorder HSDN C0003811 Cardiac rhythm disturbance C0235752 Port-wine stain HPO C0015672 Decreased energy C1336265 Stage iii mesothelioma of pleura UMLS C0151786 Weakness muscle C2981150 Uranostaphyloschisis HSDN C1384666 Decreased hearing C2350521 Gustatory perception HSDN C0036659 Sensation disorder C0033578 Prostatic neoplasms HSDN C0010200 Cough symptom C0006271 Bronchiolitis MalaCards C0042963 Symptoms vomiting C0600104 Obsessive compulsive behavior HSDN C0036572 Convulsion C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C0003079 Pupillary inequality C1962958 Hematoma adverse event HSDN C0026858 Musculoskeletal pain C0008475 Patella chondromalacia HSDN C0028081 Night sweat C0855086 Refractory nodular sclerosis classical hodgkin lymphoma UMLS C0030193 Sense of pain C0021831 Intestinal diseases HSDN C3815497 Cough C0032226 Pleural diseases HSDN C4085661 Usual severity nausea C0032965 Pregnancy complications, infectious HSDN C0016204 Fart C0810319 Other and unspecified gastrointestinal disorders UMLS C0013404 Respiratory difficulty C3273031 Hnec MalaCards C0001707 Aerophagia C1258215 Ileus HSDN C0002170 Alopecia disorders C2931426 Orofaciodigital syndrome type1 HPO C0542354 Palpebral fissure narrow C0271317 Acquired blepharophimosis UMLS C0015672 Decreased energy C0002986 Fabry disease OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0015464 Facial nerve diseases HSDN C0010520 Skin cyanosis C0039236 Tachycardia episodic HSDN C0018524 Hallucinate C0004096 Asthma HSDN C0234665 Lid retraction C0015423 Eyelid diseases UMLS C0231712 Gait waddling C0432221 Spondylometaphyseal dysplasia, 'corner fracture' type MalaCards|UMLS C0015672 Decreased energy C0023480 Leukemia, myelomonocytic, chronic UMLS C0009806 Constipate C2981401 Stage iiia colorectal cancer UMLS C0007758 Cerebellar ataxia C0033348 Language program HSDN C0033774 Skin pruritus C0149721 Left ventricular hypertrophy HSDN C0018808 Murmur C0033923 Psychomotor function HSDN C4084773 Bothered by weight gain C0003469 Anxiety disorders HSDN C4084784 Diarrhea C0016510 Foot diseases HSDN C4084723 Constipation C0006840 Candidiasis HSDN C1557397 Adverse event associated with pain C0017152 Gastritis HSDN C4085210 Usual severity pain C0079840 Milk allergy HSDN C0013362 Dysarthrias C2676254 Prickle1-related progressive myoclonus epilepsy with ataxia HPO C0022346 Yellow skin C0043102 Fiedler disease DiseaseOntology|MalaCards C0036572 Convulsion C0033800 Pseudoglioma MalaCards C0018681 Headache, cephalalgia C0023220 Leg injury HSDN C0011991 Loose stools C0014038 Encephalitis HSDN C4042891 Sleep wake disorders C0717360 Disease lyme vaccine HSDN C0015469 Facial paralysis C2239176 Liver carcinoma HSDN C2984058 Have pain C0016665 Fracture, nos with nonunion HSDN C1557397 Adverse event associated with pain C3469521 Fanconi anemia, complementation group a (disorder) HSDN C0851578 Disorder sleep C0006433 Burnout, professional HSDN C4084802 Usual severity diarrhea C0238027 Botulism, infantile MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0276275 Disease due to parvoviridae HSDN C3887638 Failure to thrive in infant C3810147 Immunodeficiency 19 MalaCards C3887638 Failure to thrive in infant C1839463 Tarp syndrome MalaCards|HPO C0010200 Cough symptom C0038356 Stomach neoplasms HSDN C3163620 Hypotension adverse event C0854176 Malignant hepato-biliary neoplasm MalaCards C1963093 Dizziness adverse event C0009240 Cognition HSDN C3274924 Have been coughing C0038940 Surgical wound dehiscence HSDN C4085211 Pain distress question C0022423 Judgement HSDN C3274924 Have been coughing C0031099 Periodontitis HSDN C0518090 Frequency of pain question C0032269 Pneumococcal infections HSDN C0162298 Stiffness joints C0220765 Weaver-like syndrome MalaCards C0034124 Pupillary disorder C0521542 Brainstem infarct HSDN C4084723 Constipation C1306794 Wound botulism OrphaNet|MalaCards C4084725 Usual severity cough C0334511 Pleural solitary fibrous tumor HSDN C0016204 Fart C0236969 Substance-related disorders HSDN C0037763 Spasm C4085311 Depression - recess HSDN C4084788 Have dizziness C0003864 Arthritis HSDN C0518090 Frequency of pain question C0560694 Bottles per feed HSDN C3274924 Have been coughing C0001973 Alcoholic intoxication, chronic HSDN C0027796 Neuralgias C0035460 Rhinitis, vasomotor HSDN C1321898 Bloody stool C0267328 Chronic gju + hemorrhage UMLS C0231218 Malaise generalized C1707549 Cutaneous lymphomatoid granulomatosis UMLS C1963091 Diarrhea adverse event C1859407 Bone dysplasia, lethal, holmgren type MalaCards C0020903 Illusion C0037369 Smoking HSDN C2984058 Have pain C0848377 Trauma to the abdomen HSDN C0011991 Loose stools C0376300 Dengue shock syndrome MalaCards C4084725 Usual severity cough C0036202 Sarcoidosis OrphaNet|HSDN|HPO|MalaCards C0012569 Double vision C0005967 Bone neoplasms HSDN C4084766 Vomiting C2240378 Cleft palate on exam HSDN C4085211 Pain distress question C0020445 Hypercholesterolemia, familial HSDN C2911647 Weight gain adverse event C0036439 Scoliosis, unspecified HSDN C3641756 Have diarrhea C3665623 Serum albumin level decreased below normal HSDN C0035078 Failure kidney C0268490 Tyrosinemia, type i MalaCards C3815497 Cough C0010414 Infection by cryptococcus neoformans HSDN C0349588 Stature short C1859782 Aniridia renal agenesis psychomotor retardation OrphaNet|MalaCards C0018524 Hallucinate C2986717 Anti-n-methyl-d-aspartate receptor encephalitis HSDN C0030552 Paralysis partial C3244301 Coverage level - family HSDN C0024902 Mastodynia C0149745 Oral ulcer HSDN C0003962 Ascites C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C3146279 Coma C1701940 Pneumonia, ventilator-associated HSDN C3641755 Have constipation C1963198 Pancreatitis adverse event HSDN C2911647 Weight gain adverse event C0018671 Head and neck neoplasms HSDN C0085636 Light sensitivity C1853197 Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa UMLS C1384666 Decreased hearing C0017601 Glaucomas HSDN C3463815 Feel fatigue C0043251 Wounds and injuries HSDN C0751837 Gait ataxic C1527311 Brain edema HSDN C1962957 Flushing adverse event C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C3898969 Have been vomiting C0027643 Neoplasm recurrence, local HSDN C0018524 Hallucinate C0027927 Neurosyphilis HSDN C0232466 Feeding difficulty C0268680 Biotin deficiency MalaCards C2911645 Weight loss adverse event C0010414 Infection by cryptococcus neoformans HSDN C0009421 Comatose C1415614 Hmgcl gene HPO C2984058 Have pain C0085129 Bronchial hyperreactivity HSDN C0239575 Fever, remittent C0743971 Fever chronic UMLS C0020673 Hypothermia (central) (local) C0003469 Anxiety disorders HSDN C0005779 Clotting C4040739 3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome MalaCards C0026821 Cramp C0022865 Obstetric labor complications HSDN C0042928 Paralysis vocal cord C0030422 Extra-adrenal paraganglioma HPO C4084774 Have weight loss C4050613 Anxiety scale (basc-2) HSDN C0034150 Skin purpura C0021400 Influenza HSDN C0007758 Cerebellar ataxia C0027627 Neoplasm metastasis HSDN C0040264 Ear ringing sound C0006436 Burning electric HSDN C0039070 Collapse fleeting C0028768 Obsessive-compulsive disorder HSDN C0700078 Deep tendon reflex decrease C2931838 Familial hdl deficiency MalaCards C4084766 Vomiting C0004659 Bacteriuria HSDN C0040485 Wryneck C2676281 Dystonia 17, torsion, autosomal recessive (disorder) MalaCards|UMLS C0023012 Delay language C1959582 Pten hamartoma tumor syndrome MalaCards C0557874 Global developmental delay C3809910 Arthrogryposis, mental retardation, and seizures MalaCards C0234132 Pyramidal sign C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards C3641756 Have diarrhea C1863236 Scid due to ada deficiency, early-onset HPO C0030552 Paralysis partial C0029423 Cartilaginous exostosis HSDN C0018524 Hallucinate C0004114 Astrocytoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1548484 Rheumatic fever vaccine HSDN C2984058 Have pain C0008732 Chylous ascites HSDN C0020639 Hypoproteinaemia C1836876 Pierson syndrome MalaCards|HPO C2096293 Ent surgical result ear vertigo C1836522 Schindler disease, type ii OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0008928 Cleidocranial dysplasia HSDN C0009080 Finger clubbing C1832940 Juvenile polyposis of stomach HPO C0018808 Murmur C0033873 Psychiatry HSDN C1963091 Diarrhea adverse event C0010674 Cystic fibrosis HSDN C4042891 Sleep wake disorders C2239176 Liver carcinoma HSDN C4085210 Usual severity pain C1306710 Facial asymmetry HSDN C4085548 Usual severity dizziness C0037313 Sleep HSDN C0031256 Petechia C2930957 Hantavirosis MalaCards C0018991 Paralysis one side of body C0238096 Embolism, paradoxical HSDN C0018784 Deafness sensorineural C2931928 Mitochondrial cytopathy MalaCards C4085661 Usual severity nausea C0025063 Mediastinal neoplasms HSDN C4084766 Vomiting C1962983 Cataract adverse event HSDN C0040264 Ear ringing sound C0265321 Wyburn-mason syndrome MalaCards C0234146 Absent reflex C1842898 Muscular dystrophy, congenital, due to partial lama2 deficiency HPO C3274924 Have been coughing C0029456 Osteoporosis HSDN C2024893 Cardiovascular surgery result: fatigue C1861848 Paragangliomas 4 MalaCards C0002170 Alopecia disorders C3536797 Ichthyosis congenita ii MalaCards C0151908 Dry skin C3494506 Pseudohypoparathyroidism, type ia MalaCards C0030554 Abnormal sensation C1556682 Adverse event associated with infection HSDN C0017181 Gastrointestinal bleed C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C4084725 Usual severity cough C0009240 Cognition HSDN C3463815 Feel fatigue C0021818 Intervertebral disk displacement HSDN C0522224 Palsied C0018188 Granuloma HSDN C0234523 Apraxia, classic C0037019 Shy-drager syndrome HSDN C0917816 Deficiency mental C0268140 Xeroderma pigmentosum, group f HPO C1999266 Depression adverse event C3554605 Mc3dn2 MalaCards C1999266 Depression adverse event C0268322 Chester-type porphyria HPO C4084788 Have dizziness C0001418 Adenocarcinoma HSDN C0018772 Deafness C1865794 Rhyns syndrome OrphaNet|MalaCards C1838869 Proximal neurogenic muscle weakness C2931347 Cardiac form of generalized glycogenosis MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0403447 Chronic kidney insufficiency HSDN C0024032 Birth weight subnormal C1842465 Lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones OrphaNet|MalaCards C0848203 Male pelvic pain C0221752 Rbc urine HSDN C4084921 Usual severity itching C3276706 Small fiber neuropathy MalaCards C0040034 Thrombocytopenia C0268608 Deficiency of dihydrofolate reductase MalaCards C0424755 Fever symptoms C0032963 Pregnancy complications, cardiovascular HSDN C0557874 Global developmental delay C0795832 9p tetrasomy OrphaNet|MalaCards C0851578 Disorder sleep C1546654 Specimen source codes - granuloma HSDN C0577567 Mass of urogenital structure C0403783 Sperm granuloma of epididymis UMLS C0026826 High muscle tone C0220765 Weaver-like syndrome MalaCards|HPO C3887873 Hearing loss C0041948 Uremia HSDN C1963170 Hypothermia adverse event C0040127 Thyroid crisis HSDN C0037317 Sleep disturbance C0851578 Sleep disorders UMLS C3274924 Have been coughing C0152054 Therapeutic touch HSDN C0040264 Ear ringing sound C0221759 Brachial plexus neuritis HSDN C3815497 Cough C0027746 Nerve degeneration HSDN C0020615 Hypoglycemia nos C0878683 Pituitary dwarfism type 3 MalaCards C0042571 Vertigo subjective C2240374 Eosinophil count raised HSDN C0033774 Skin pruritus C0242698 Ventricular dysfunction, left HSDN C0518090 Frequency of pain question C2242765 Acquired spondylolisthesis HSDN C0003862 Pain joint C1548578 Location characteristic id - smoking HSDN C4084788 Have dizziness C0007273 Carotid artery diseases HSDN C2911647 Weight gain adverse event C0026946 Mycoses HSDN C1963170 Hypothermia adverse event C0003850 Arteriosclerosis HSDN C0851578 Disorder sleep C0015934 Fetal growth retardation HSDN C3887873 Hearing loss C0003962 Ascites HSDN C0036572 Convulsion C3698078 Postoperative status epilepticus UMLS C0234428 Consciousness disturbance C0234447 Narcosis UMLS C0039070 Collapse fleeting C0344315 Depressed mood HSDN C0018681 Headache, cephalalgia C0020564 Hypertrophy HSDN C1384666 Decreased hearing C0038661 Suicide HSDN C0018991 Paralysis one side of body C0033845 Pseudotumor cerebri HSDN C0013528 Echo speech C0236792 Asperger syndrome HSDN C2242996 Tingling C1720416 Episodic ataxia type 2 (disorder) MalaCards|HPO C0003079 Pupillary inequality C0037304 Skull fracture HSDN C2096293 Ent surgical result ear vertigo C0282492 Sneddon syndrome OrphaNet|HPO|MalaCards C2984058 Have pain C0022362 Jaw diseases HSDN C1000483 Genus anemia C3179349 Gastrointestinal stromal sarcoma MalaCards|HPO C0278152 Hemifacial spasms C0025286 Meningioma MalaCards C1069915 Vertigo C0001807 Aggressive behavior HSDN C4085211 Pain distress question C0008928 Cleidocranial dysplasia HSDN C0020673 Hypothermia (central) (local) C0036341 Schizophrenia HSDN C2984058 Have pain C0027429 Nasal obstruction present finding HSDN C4084773 Bothered by weight gain C0025149 Medulloblastoma HSDN C0413252 Hypothermia due to exposure C0796561 Melanoma vaccines HSDN C0042571 Vertigo subjective C0020550 Hyperthyroidism HSDN C0860603 Anxiety symptom C0687720 Central diabetes insipidus OrphaNet|MalaCards C3815569 Have increased appetite question C1846171 Lissencephaly, x-linked, 2 MalaCards C0033377 Caudal displacement C1836123 Goldberg-shprintzen megacolon syndrome OrphaNet|HPO C0018681 Headache, cephalalgia C0265301 Sclerosteosis HPO C0917816 Deficiency mental C0010273 Craniofacial dysostosis MalaCards|HPO C4085210 Usual severity pain C0017668 Focal glomerulosclerosis HSDN C1963281 Vomiting adverse event C0275911 Tuberculosis of intestines MalaCards C4084725 Usual severity cough C0036467 Scrofula MalaCards C0575081 Abnormal gait C0030567 Parkinson disease MalaCards C0011991 Loose stools C0016952 Galactosemias MalaCards C0557874 Global developmental delay C0342727 3-@methylglutaconic aciduria, type i OrphaNet|HPO|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0002989 Epithelioid hemangioma of skin HSDN C0007758 Cerebellar ataxia C1848813 Thyrocerebral-retinal syndrome MalaCards C0030554 Abnormal sensation C1842534 Dystonia 18 (disorder) OrphaNet|HPO|MalaCards C0026821 Cramp C0007959 Charcot-marie-tooth disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0032326 Pneumothorax HSDN C0030554 Abnormal sensation C0752191 Central nervous system schistosomiasis HSDN C4084766 Vomiting C0034072 Cor pulmonale HSDN C0033774 Skin pruritus C0034088 Pulmonary valve insufficiency HSDN C4085211 Pain distress question C0024137 Lupus erythematosus, cutaneous HSDN C0243026 Generalized infection C0042781 Visceral myopathy MalaCards C4084775 Usual severity weight loss C0038013 Ankylosing spondylitis HSDN C0038002 Spleen enlargement C2930971 Acroosteolysis dominant type MalaCards|HPO C0013404 Respiratory difficulty C1333125 Combined small cell carcinoma of lung UMLS C0042963 Symptoms vomiting C0023676 Life style HSDN C4085642 Level of joint stiffness C0026709 Mucopolysaccharidosis vi OrphaNet|HPO|MalaCards C0015970 Fever unknown origin C0036130 Salpingitis HSDN C0008031 Pain chest C0017168 Gastroesophageal reflux disease UMLS C0033377 Caudal displacement C0376524 Branchio-oculo-facial syndrome MalaCards|HPO C0036572 Convulsion C0796206 Atkin syndrome MalaCards|UMLS C3539890 Pelvic pain causes awakening at night C0010709 Cyst HSDN C4084768 Usual severity vomiting C2240378 Cleft palate on exam HSDN C4084727 Cough frequency C0033873 Psychiatry HSDN C0018524 Hallucinate C0014836 Escherichia coli infections HSDN C1963071 Back pain adverse event C0031037 Periarthritis HSDN C0015672 Decreased energy C0854795 Resectable hepatic malignant neoplasm MalaCards C0850758 Pain pelvic C0027095 Myosarcoma HSDN C0019825 Voice hoarseness C0020538 Hypertensive disease HSDN|UMLS C0012833 Dizzy C0036690 Septicemia HSDN C0424755 Fever symptoms C0302363 Bang disease MalaCards C0020538 Hbp C1567741 Alport syndrome OrphaNet C4084764 Shortness of breath C0796274 Brown-vialetto-van laere syndrome MalaCards C0234376 Tremor action C0018553 Hamartoma syndrome, multiple HPO|UMLS C0424755 Fever symptoms C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0018681 Headache, cephalalgia C0017658 Glomerulonephritis HSDN C0013395 Indigestion C0007786 Brain ischemia HSDN C0033377 Caudal displacement C0796179 Teebi syndrome MalaCards C1963184 Nystagmus adverse event C1858677 Leber congenital amaurosis 3 (disorder) MalaCards|HPO C0011570 Monopolar depression C2936741 Syndrome xxyy OrphaNet|MalaCards C0162429 Dietary deficiency C1384687 Ancylostomiasis due to ancylostoma duodenale MalaCards C0018681 Headache, cephalalgia C1333071 Chordoma of clivus UMLS C0034150 Skin purpura C0025202 Melanoma HSDN C0013395 Indigestion C0024299 Lymphoma HSDN C0018681 Headache, cephalalgia C0162309 Adrenoleukodystrophy OrphaNet|MalaCards C4085548 Usual severity dizziness C1762616 Meningioma, benign, no icd-o subtype HSDN C1963071 Back pain adverse event C0027663 Neoplasms, multiple primary HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0282550 Persian gulf syndrome HSDN C0344435 Ventricular fibrillation by ecg finding C1838527 Long qt syndrome 3, acquired, susceptibility to HPO C1288081 Inflammatory testicular mass C0039584 Testicular diseases UMLS C0151908 Dry skin C1848410 Xeroderma pigmentosum, variant type OrphaNet|HPO|MalaCards C0035229 Respiratory function impaired C2931220 Symmetrical infantile thalamic degeneration OrphaNet C0009792 Consciousness disorder C0018802 Congestive heart failure HSDN C4084726 Distress cough C1963084 Colitis adverse event HSDN C1519353 Skin eruption papular C1836122 Sarcoidosis, early-onset MalaCards C0023014 Developmental disorder language C1579931 Depressed - symptom HSDN C0003469 Anxiety disorder C0342200 Endemic cretinism MalaCards C0497247 Blood pressure elevation C1836122 Sarcoidosis, early-onset MalaCards C0003862 Pain joint C1963148 Iron overload adverse event HSDN C0152227 Tearing excessive C1852551 Epithelial recurrent erosion dystrophy MalaCards|HPO C0018780 Frequencies hearing high loss C2749137 Retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness HPO C0010520 Skin cyanosis C0040962 Tricuspid valve prolapse HSDN C0015300 Ocular proptosis C2931888 Pfeiffer type acrocephalosyndactyly MalaCards C4084767 Bothered by vomiting C0346303 Thyrotroph adenoma OrphaNet|MalaCards C0042571 Vertigo subjective C2984299 Asthma pathway HSDN C4084723 Constipation C0025289 Meningitis HSDN C1963065 Apnea adverse event C0017638 Glioma HSDN C0242936 Center pain C1739395 Takotsubo cardiomyopathy HSDN C0018524 Hallucinate C0030767 Grouping peer HSDN C3463815 Feel fatigue C0008625 Chromosome aberrations HSDN C4084766 Vomiting C0268595 Glutaric aciduria, type 1 OrphaNet|HPO C1384666 Decreased hearing C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|MalaCards C1962972 Proteinuria adverse event C0027439 Nasopharyngeal neoplasms HSDN C0557874 Global developmental delay C3809606 Epileptic encephalopathy, early infantile, 17 MalaCards C4085211 Pain distress question C0019557 Hip fx HSDN C4084784 Diarrhea C0206526 Tuberculosis, multidrug-resistant HSDN C0413252 Hypothermia due to exposure C0004935 Animal ethology HSDN C0424755 Fever symptoms C0032024 Pityriasis HSDN C1279888 Proteinuria of undiagnosed cause C0497327 Dementia HSDN C4084802 Usual severity diarrhea C0006147 Breast fed HSDN C0233844 Awkwardness C1299884 Eosinophilic myositis (disorder) HPO C1959630 Eye pain adverse event C0024440 Macular edema, cystoid HSDN C0150055 Pain chronic C0027663 Neoplasms, multiple primary HSDN C4085862 Bothered by nausea C0016483 Food preferences HSDN C3146279 Coma C1552262 Nurse practitioner - family HSDN C3641756 Have diarrhea C0040560 Toxoplasmosis, congenital MalaCards C0344315 Mood depressed C0018523 Hallervorden-spatz syndrome MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0009404 Colorectal neoplasms HSDN C0016382 Cutaneous vascular engorgement C0020473 Hyperlipidemia HSDN C1557397 Adverse event associated with pain C0206620 Lymphangioma, cystic HSDN C0004134 Dyssynergia C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO|UMLS C0034150 Skin purpura C0042266 Vaginismus HSDN C0085631 Abnormal excitement C0751157 Fraxe syndrome UMLS C0019209 Large liver C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0233844 Awkwardness C1849096 Infantile onset spinocerebellar ataxia MalaCards|HPO|UMLS C0040822 D tremors C0344434 Atrial fibrillation ecg HSDN C4084724 Usual severity constipation C1836929 Emanuel syndrome OrphaNet|MalaCards C0349588 Stature short C0271695 Rabson-mendenhall syndrome OrphaNet|HPO C0011168 Disorder deglutition C2750220 Karak syndrome MalaCards|HPO C0018991 Paralysis one side of body C0016053 Fibromyalgia HSDN C0522224 Palsied C0161405 Cranial nerve iv injury HSDN C0015970 Fever unknown origin C0751878 Vasculitis, central nervous system HSDN C0008031 Pain chest C1866983 Scleroderma, familial progressive MalaCards C0024031 Back pain lower back C0009395 Color perception HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C2711591 Infection by anisakidae HSDN C0039070 Collapse fleeting C0036323 Schistosomiasis HSDN C4084727 Cough frequency C3463824 Myelodysplastic syndrome HSDN C0424755 Fever symptoms C0037774 Spatial behavior HSDN C0518090 Frequency of pain question C0428478 Serum triglycerides raised HSDN C4084802 Usual severity diarrhea C0719874 Diaper rash brand HSDN C0399411 Discoloration of teeth due to drugs C0277579 Drug-related disorders UMLS C0019079 Bloody sputum C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0034150 Skin purpura C2911643 Encounter due to family history of osteoporosis HSDN C2029884 Hearing loss by exam C0022116 Ischemia HSDN C1963087 Constipation adverse event C0002989 Epithelioid hemangioma of skin HSDN C4085222 Nausea C1856403 Etfb deficiencies HPO C0018784 Deafness sensorineural C0266526 Norrie disease MalaCards|HPO C4084802 Usual severity diarrhea C0268407 Senile cardiac amyloidosis MalaCards C3887784 Decreased urine output C0009492 Compartment syndromes HSDN C0004604 Pain back C1532253 Sedentary lifestyle HSDN C0243026 Generalized infection C0018203 Chronic granulomatous disease MalaCards|HPO C0030554 Abnormal sensation C0700095 Central neuroblastoma HSDN C2128958 Middle-night awakening with a choking sensation C0393761 Fitful sleep UMLS C0004093 Asthenia C0038354 Stomach diseases HSDN C3539896 Pelvic pain occurs with urination C0023467 Leukemia, myelocytic, acute HSDN C0037763 Spasm C0027686 Pathologic neovascularization HSDN C3541349 Syncope C0023676 Life style HSDN C0042024 Urine incontinence C0015734 Stool impacted HSDN C0242936 Center pain C0005694 Bladder neck obstruction HSDN C0007758 Cerebellar ataxia C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084766 Vomiting C0038454 Cerebrovascular accident HSDN C0020455 Hypergammaglobulinemia C0037023 Sialadenitis HSDN C4084784 Diarrhea C0005779 Blood coagulation disorders HSDN C4084774 Have weight loss C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C4084773 Bothered by weight gain C0007787 Transient ischemic attack HSDN C2984057 Have nausea C0024437 Macular degeneration HSDN C0036572 Convulsion C0001139 Acinetobacter infection HSDN C4085317 Diarrhea frequency C0024299 Lymphoma HSDN C1549543 Administration method - pain C0029124 Optic atrophy HSDN C0041105 Jaw spasm C0399526 Class iii malocclusion HSDN C1549543 Administration method - pain C0037278 Skin diseases, infectious HSDN C0034124 Pupillary disorder C0752282 Congenital structural myopathy HSDN C1963237 Insomnia adverse event C0022134 Islet cell adenoma MalaCards C0518090 Frequency of pain question C0009480 Community psychiatry HSDN C0026821 Cramp C0015423 Eyelid diseases HSDN C0020615 Hypoglycemia nos C2717876 Aciduria, propionic OrphaNet|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0019699 Hiv seropositivity HSDN C0000737 Abdomen pain C0025063 Mediastinal neoplasms HSDN C1549543 Administration method - pain C0030569 Secondary parkinson disease HSDN C0042963 Symptoms vomiting C0018552 Hamartoma HSDN C4049602 Hyperactivity C0033922 Psychomotor disorders MalaCards C0018524 Hallucinate C0014849 Esophageal and gastric varices HSDN C4085210 Usual severity pain C0043528 Zoonoses HSDN C2315100 Pediatric failure to thrive C2748910 Rett syndrome, atypical MalaCards C1963281 Vomiting adverse event C0035801 Diseases rodent HSDN C4085317 Diarrhea frequency C3810147 Immunodeficiency 19 MalaCards C0349588 Stature short C2673375 Mucolipidosis iii alpha beta, atypical HPO C1549543 Administration method - pain C0025281 Meniere disease HSDN C0426579 Anorexia symptom C0033348 Language program HSDN C0022346 Yellow skin C1552262 Nurse practitioner - family HSDN C4085862 Bothered by nausea C0008049 Chicken pox DiseaseOntology|HSDN|MalaCards C0036572 Convulsion C3809006 Cardiofaciocutaneous syndrome 3 MalaCards C0030232 Color loss C0265428 9p+ syndrome MalaCards C0040264 Ear ringing sound C0521542 Brainstem infarct HSDN C0349588 Stature short C0028326 Noonan syndrome OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C1857341 Deafness, conductive, with malformed external ear OrphaNet|MalaCards C0349588 Stature short C0432215 Progressive pseudorheumatoid dysplasia OrphaNet|HPO C4085211 Pain distress question C0042341 Varicocele HSDN C0018520 Breath odor C0032241 Pleuropneumonia HSDN C1962972 Proteinuria adverse event C0021390 Inflammatory bowel diseases HSDN C3539893 Pelvic pain occurs with intercourse C0010356 Cross infection HSDN C0013604 Edematous C4042784 Feeding and eating disorders HSDN C2919142 Short stature adverse event C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C0000727 Abdomen acute C0019284 Diaphragmatic hernia HSDN C2315100 Pediatric failure to thrive C0796208 Mental retardation, x-linked 3 HPO C3539892 Pelvic pain in front C0037929 Spinal cord injuries HSDN C0008031 Pain chest C0021841 Intestinal neoplasms HSDN C4084784 Diarrhea C0035012 Reiter syndrome OrphaNet|MalaCards C1962972 Proteinuria adverse event C0021655 Insulin resistance HSDN C0027066 Myoclonic jerking C1963067 Atrial fibrillation adverse event HSDN C0033774 Skin pruritus C0281361 Adenocarcinoma of pancreas UMLS C4042891 Sleep wake disorders C0020625 Hyponatremia HSDN C1557397 Adverse event associated with pain C0027831 Neurofibromatosis 1 HSDN C0241137 Skin pallor C0011615 Dermatitis, atopic HSDN C0038990 Sweats C1849320 Sandhoff disease, adult type HPO C4084776 Weight loss C2073625 X-ray of chest: pleural effusion HSDN C0027497 Queasy C0024117 Chronic obstructive airway disease HSDN C4084776 Weight loss C0027697 Nephritis HSDN C4084724 Usual severity constipation C3178970 Entrapment, pudendal nerve MalaCards C2203646 Jaundice C0155862 Streptococcal pneumonia HSDN C3641756 Have diarrhea C0024523 Malabsorption syndrome MalaCards C0018520 Breath odor C0034194 Pyloric stenosis HSDN C0917816 Deficiency mental C3810001 Combined oxidative phosphorylation deficiency 18 MalaCards C4085210 Usual severity pain C0005694 Bladder neck obstruction HSDN C1963184 Nystagmus adverse event C2931092 Maternally inherited leigh syndrome MalaCards C1963170 Hypothermia adverse event C1552527 Clinic / center - developmental disabilities HSDN C4085211 Pain distress question C0041313 Hepatic tuberculosis HSDN C1579931 Depressed - symptom C0162532 Variegate porphyria MalaCards|HPO C1963252 Tremor adverse event C0022735 Klinefelter syndrome HSDN C0024031 Back pain lower back C0085762 Alcohol abuse UMLS C0004134 Dyssynergia C0036421 Systemic scleroderma HSDN C0018772 Deafness C1961100 Erectile dysfunction adverse event HSDN C0206160 Retic count elevated C0242723 Parasitemia HSDN C0020505 Excessive eating C0013011 Dominance subordination HSDN C3665492 Pigmentations C0206735 Melanoma, amelanotic MalaCards C0162298 Stiffness joints C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0014358 Enterocolitis, pseudomembranous HSDN C0030193 Sense of pain C1696469 Shin splints HSDN C0221263 Cafe au lait spot C0003490 Aortic arch syndrome HSDN C0038002 Spleen enlargement C0036996 Short rib-polydactyly syndrome MalaCards C2232697 Mood symptoms C0020517 Hypersensitivity UMLS C2315100 Pediatric failure to thrive C0018818 Ventricular septal defects HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0039128 Syphilis HSDN C0162298 Stiffness joints C1835614 Hereditary hyperexplexia MalaCards C0030193 Sense of pain C0026948 Mycosis fungoides HSDN C2911645 Weight loss adverse event C0022758 Kap HSDN C0016204 Fart C0007570 Celiac disease HSDN C3829611 Nausea frequency C0036240 Response, satiety HSDN C0030193 Sense of pain C0026654 Moyamoya disease HSDN C0003862 Pain joint C0027663 Neoplasms, multiple primary HSDN C4084726 Distress cough C0029408 Degenerative polyarthritis HSDN C0019079 Bloody sputum C0001973 Alcoholic intoxication, chronic HSDN C2364082 Hyposmia C1846862 Parkinson disease 8 (disorder) UMLS C1963281 Vomiting adverse event C0524812 Intracranial hypotension HSDN C0031911 Pigment deposition C1876175 Ataxia-telangiectasia variant MalaCards C0019209 Large liver C1835664 Tylosis with esophageal cancer MalaCards C0003862 Pain joint C4049638 Cutaneous small vessel vasculitis MalaCards C0027066 Myoclonic jerking C0003873 Rheumatoid arthritis HSDN C0038002 Spleen enlargement C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0013404 Respiratory difficulty C1547044 Kind of quantity - smell HSDN C0151686 Growth retardation C3150674 Chromosome 15q24 deletion syndrome HPO C0023014 Developmental disorder language C2028283 History of premature birth HSDN C0027796 Neuralgias C0520946 Emotional hypersensitivity HSDN C0018681 Headache, cephalalgia C2985170 Multifocal glioblastomas UMLS C1000483 Genus anemia C0085292 Stiff-person syndrome MalaCards C0018772 Deafness C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet C0277799 Fever intermittent C0013364 Dysautonomia, familial HPO C0042963 Symptoms vomiting C4084909 Depression subordinate domain HSDN C0043094 Weight gain C0029882 Otitis media HSDN C0042928 Paralysis vocal cord C0020538 Hypertensive disease HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C3665346 Loss sight C0751664 Canavan disease, neonatal OrphaNet|HPO C3274924 Have been coughing C0003493 Aortic diseases HSDN C4084776 Weight loss C1963266 Uveitis adverse event HSDN C0577560 Eye mass C1867616 Dermoid choristoma of eye proper UMLS C0151908 Dry skin C0026363 Mohr-claussen syndrome MalaCards C2237041 Shox gene with short stature C2931902 Acute brachial neuritis MalaCards C0042571 Vertigo subjective C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0860603 Anxiety symptom C0271865 Autoimmune hypoparathyroidism MalaCards C3539896 Pelvic pain occurs with urination C0041954 Ureteral diseases and syndromes HSDN C4085210 Usual severity pain C0043246 Laceration HSDN C0037316 Not enough sleeping C0311277 Obesity, abdominal HSDN C0518090 Frequency of pain question C0041313 Hepatic tuberculosis HSDN C1090821 Sepsis C1801959 Histiocytic medullary reticulosis (disorder) MalaCards C0007166 Cardiac output decreased C0340629 Aortic aneurysm without mention of rupture nos HSDN C0349588 Stature short C2931534 Cloverleaf skull and bone dysplasias MalaCards C1963071 Back pain adverse event C2350572 Illness behavior HSDN C1963091 Diarrhea adverse event C1623041 Breast-fed HSDN C2024893 Cardiovascular surgery result: fatigue C0242992 Multiple chemical sensitivity HSDN C3887873 Hearing loss C0023467 Leukemia, myelocytic, acute HSDN C0009460 Communication impairment C0175702 Williams syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043253 Trauma blunt HSDN C0578738 Epitrochlear lymphadenopathy C1264154 Upper extremity lymphadenopathy UMLS C0020673 Hypothermia (central) (local) C0005591 Avian disease HSDN C0015970 Fever unknown origin C0003504 Aortic valve insufficiency HSDN C0037771 Paraparesis spastic C0205710 Alpers syndrome (disorder) OrphaNet|HPO|MalaCards C3539893 Pelvic pain occurs with intercourse C0036864 Sexual relations HSDN C1069915 Vertigo C0003838 Arterial occlusive diseases HSDN C2237041 Shox gene with short stature C1852542 Cdo syndrome MalaCards C0036572 Convulsion C0795833 Kleefstra syndrome HPO|UMLS C0000737 Abdomen pain C0024117 Chronic obstructive airway disease HSDN C0020673 Hypothermia (central) (local) C0039336 Gustatory sense HSDN C0151311 Cranial nerve palsy C1443900 Inhalational botulism OrphaNet|MalaCards C0700590 Diaphoresis excessive C0080333 Weber-cockayne syndrome OrphaNet|HPO C0557874 Global developmental delay C0151516 Thyroid hypoplasia OrphaNet|HPO C0002965 Crescendo angina C0035229 Respiratory insufficiency HSDN C0018784 Deafness sensorineural C0022541 Kearns-sayre syndrome MalaCards C1963281 Vomiting adverse event C0013010 Cerebral lateralization HSDN C0008031 Pain chest C2752007 Congenital disorder of glycosylation, type io MalaCards C0085602 Polydypsia C1260386 Glucocorticoid-remediable aldosteronism HPO C1963093 Dizziness adverse event C0022701 Kinesthesia HSDN C1069915 Vertigo C0018671 Head and neck neoplasms HSDN C3541349 Syncope C0022661 Kidney failure, chronic HSDN C3539895 Pelvic pain occurs with bowel movement C0458219 Complex regional pain syndromes HSDN C4084802 Usual severity diarrhea C0005659 Bite sting HSDN C0424755 Fever symptoms C0376550 Astroviridae infection HSDN C0039070 Collapse fleeting C0027051 Myocardial infarction UMLS C4084773 Bothered by weight gain C0020179 Huntington disease HSDN C0151908 Dry skin C3281084 Congenital disorder of glycosylation, type ir MalaCards C0237326 Defecation pain C1514428 Primary peritoneal carcinoma MalaCards C0004604 Pain back C2945560 Hemolytic HSDN C0018681 Headache, cephalalgia C0334583 Pilocytic astrocytoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0034072 Cor pulmonale HSDN C0151786 Weakness muscle C0019151 Hepatic encephalopathy HSDN C2029884 Hearing loss by exam C0036690 Septicemia HSDN C0018524 Hallucinate C0236642 Pick disease of the brain HSDN C0015672 Decreased energy C0020550 Hyperthyroidism HSDN C1557397 Adverse event associated with pain C0041955 Ureteral neoplasms HSDN C4084767 Bothered by vomiting C0239189 Disaccharide intolerance MalaCards C0857305 Thrombocytopenia purpura C0005967 Bone neoplasms HSDN C0013604 Edematous C0085083 Ovarian hyperstimulation syndrome HSDN C2984058 Have pain C0161410 Accessory nerve injuries HSDN C0497247 Blood pressure elevation C0221406 Pituitary-dependent cushing's disease OrphaNet|HPO C0020578 Hyperventilate C0022865 Obstetric labor complications HSDN C0349489 Fetal hypoxia C0014068 Encephalomalacia HSDN C0042963 Symptoms vomiting C0036690 Septicemia HSDN C0039070 Collapse fleeting C0021843 Intestinal obstruction HSDN C0241165 Skin thickening C0011644 Scleroderma OrphaNet C0476273 Distress respiratory C1859726 Arterial tortuosity syndrome MalaCards C0162292 Extraocular palsy C2931024 Moebius axonal neuropathy hypogonadism OrphaNet|MalaCards C0242936 Center pain C0016662 Fracture open HSDN C0004604 Pain back C2984572 Malaria pathway HSDN C0242936 Center pain C0037413 Social dominance HSDN C1963087 Constipation adverse event C0022661 Kidney failure, chronic HSDN C3829611 Nausea frequency C0002726 Amyloidosis HSDN C0002962 Angina C0428977 Bradycardia HSDN C0030193 Sense of pain C0003886 Arthrogryposis HSDN C0015300 Ocular proptosis C1850155 Torg-winchester syndrome MalaCards|HPO C1963177 Muscle pain adverse event C0014805 Primary erythermalgia MalaCards C0151786 Weakness muscle C1535916 Pelvic floor muscle weakness UMLS C4085210 Usual severity pain C0752308 Hypoxia-ischemia, brain HSDN C4085211 Pain distress question C0018889 Helminthiasis HSDN C0424755 Fever symptoms C1704212 Embolism embolus HSDN C0024031 Back pain lower back C1963119 Stomach ulcer adverse event HSDN C0023530 Leukopenia C0342337 Insulin resistance syndrome, type b OrphaNet|MalaCards C4084775 Usual severity weight loss C0025517 Metabolic diseases HSDN C0026838 Spasticity muscle C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C2984058 Have pain C1366535 Avp gene HSDN C0242936 Center pain C0035333 Retinitis HSDN C4085222 Nausea C0022336 Creutzfeldt-jakob disease HSDN C1963093 Dizziness adverse event C0020701 Somatization disorder HSDN C0027497 Queasy C0343398 Cyclosporiases HSDN C0020672 Body temperature decreased C0028768 Obsessive-compulsive disorder HSDN C0151686 Growth retardation C3150750 Agammaglobulinemia 2, autosomal recessive MalaCards C0040485 Wryneck C0154723 Migraine with aura HSDN C3146279 Coma C1622510 Neurocytoma MalaCards C0007384 Cataplexy C0220756 Niemann-pick disease, type c MalaCards|HPO C0206160 Retic count elevated C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards|HPO C4084726 Distress cough C0016045 Fibroma HSDN C0043068 Friderichsen-waterhouse syndrome C1704212 Embolism embolus HSDN C3203358 Alveolar hypoventilation C0041296 Tuberculosis HSDN C4084723 Constipation C0014805 Primary erythermalgia MalaCards|HPO C0019209 Large liver C0031069 Familial mediterranean fever HPO C2029884 Hearing loss by exam C0027643 Neoplasm recurrence, local HSDN C0000727 Abdomen acute C0750426 Wbc elevated HSDN C0454644 Delayed language development C0033922 Psychomotor disorders MalaCards C0018777 Deafness, conductive C3714899 Symphalangism, proximal, 1a MalaCards C0349588 Stature short C1862178 Cole carpenter syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0162790 Harassment sexual HSDN C0030193 Sense of pain C0039841 Thiamine deficiency HSDN C4084767 Bothered by vomiting C0524851 Neurodegenerative disorders HSDN C0028738 Nystagmus C3888385 Peroxisome biogenesis disorder 7a (zellweger) MalaCards C3541349 Syncope C0022116 Ischemia HSDN C3887873 Hearing loss C1299262 Sarcoma - category (morphologic abnormality) HSDN C1384666 Decreased hearing C1865794 Rhyns syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0028945 Oligodendroglioma HSDN C0042024 Urine incontinence C0014347 Enterobacteriaceae infections HSDN C1963281 Vomiting adverse event C0002949 Aneurysm, dissecting HSDN C0015672 Decreased energy C1963083 Cholecystitis adverse event HSDN C3539892 Pelvic pain in front C0017181 Gastrointestinal hemorrhage HSDN C0011991 Loose stools C0162627 Skin diseases, bacterial HSDN C0019572 Hairiness C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C0086565 Liver function abnormal C2936664 Acquired hypogammaglobulinemia MalaCards C0042798 Vision dim C0271092 Progressive cone dystrophy (without rod involvement) OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0035435 Rheumatism HSDN C1963137 Hydrocephalus adverse event C0016395 Focal dermal hypoplasia MalaCards|HPO C1579931 Depressed - symptom C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C0000737 Abdomen pain C0152724 Tuberculosis of intestines and mesenteric glands DiseaseOntology|MalaCards C4084724 Usual severity constipation C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C1510417 Apraxia of gait C0033835 Pseudopseudohypoparathyroidism HSDN C1963065 Apnea adverse event C0002063 Alkalosis HSDN C0036572 Convulsion C4039464 Complex partial epileptic seizure of frontal lobe UMLS C0035229 Respiratory function impaired C0265275 Jeune thoracic dystrophy OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0030305 Pancreatitis HSDN C4085317 Diarrhea frequency C0003650 Apudoma HSDN C0018784 Deafness sensorineural C1858108 Microcephaly, primary autosomal recessive, 3 MalaCards|HPO C2237041 Shox gene with short stature C1844887 Catel manzke syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0005779 Clotting C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0036572 Convulsion C0836924 Thrombocytosis HSDN C0018772 Deafness C0034089 Pulmonary valve stenosis HSDN C0042963 Symptoms vomiting C2987173 Pancreatic solid serous adenoma UMLS C0013404 Respiratory difficulty C0014461 Granuloma eosinophilic MalaCards C4084727 Cough frequency C0020615 Hypoglycemia HSDN C0042571 Vertigo subjective C3280866 Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) MalaCards C0600142 Flash hot C0040053 Thrombosis HSDN C4085211 Pain distress question C0005426 Biliary tract neoplasm HSDN C0401158 Vomiting after git surgery C1285297 Gastrointestinal complication of procedure UMLS C2029884 Hearing loss by exam C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0012833 Dizzy C1962958 Hematoma adverse event HSDN C3887873 Hearing loss C0027663 Neoplasms, multiple primary HSDN C0033377 Caudal displacement C0268337 Ehlers-danlos syndrome, type 3 (disorder) HPO C1384666 Decreased hearing C1864689 Microphthalmia, syndromic 6 (disorder) MalaCards|HPO C0518090 Frequency of pain question C0030470 Paranasal sinus neoplasms HSDN C4084767 Bothered by vomiting C3149848 Variegate porphyria, homozygous variant HPO C0028738 Nystagmus C2930852 Zellweger leukodystrophy MalaCards C2911647 Weight gain adverse event C0035243 Respiratory tract infections HSDN C1963091 Diarrhea adverse event C1319688 Blister dose form HSDN C0151686 Growth retardation C1847572 Seckel syndrome 2 MalaCards|HPO C0018784 Deafness sensorineural C0041409 Turner syndrome, male MalaCards|HSDN|HPO C4085549 Dizziness C0027686 Pathologic neovascularization HSDN C0020903 Illusion C0036349 Paranoid schizophrenia HSDN C0011991 Loose stools C2984302 Leishmaniasis infection pathway HSDN C4084767 Bothered by vomiting C0524620 Metabolic syndrome x HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024958 Maxillary sinus neoplasms HSDN C4085862 Bothered by nausea C1546949 Event consequence - death HSDN C0006370 Bulimia C0037279 Skin diseases, metabolic HSDN C0018784 Deafness sensorineural C0432348 Crandall syndrome OrphaNet|MalaCards C0151889 Reflexes tendon increased C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C3641756 Have diarrhea C0400827 Proctitis radiation MalaCards C0242936 Center pain C0042165 Anterior uveitis HSDN C0015672 Decreased energy C0238288 Muscular dystrophy, facioscapulohumeral HSDN C3539891 Pelvic pain to the rear C0432264 Axial osteosclerosis MalaCards C4085211 Pain distress question C0026705 Mucopolysaccharidosis ii HSDN C1963065 Apnea adverse event C0036391 Schwartz-jampel syndrome MalaCards|HPO C0000737 Abdomen pain C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C2984058 Have pain C0005119 Bereavement HSDN C0018784 Deafness sensorineural C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C0036572 Convulsion C3553230 Congenital disorder of glycosylation, type iil MalaCards|UMLS C4085317 Diarrhea frequency C0012242 Digestive system disorders HSDN C0162298 Stiffness joints C1862471 Arthrogryposis, distal, type 6 OrphaNet|MalaCards C3641756 Have diarrhea C0518449 Control of hip fracture risk HSDN C0004604 Pain back C0037205 Sirenomelia HPO C0018991 Paralysis one side of body C0027092 Myopia HSDN C3539896 Pelvic pain occurs with urination C0023890 Liver cirrhosis HSDN C3898969 Have been vomiting C0029134 Optic neuritis HSDN C0009806 Constipate C0037369 Smoking HSDN C1549543 Administration method - pain C0023976 Long qt syndrome HSDN C3815497 Cough C0008370 Cholestasis HSDN C0015672 Decreased energy C0005659 Bite sting HSDN C0242936 Center pain C0020876 Ileal neoplasms HSDN C1963091 Diarrhea adverse event C0008733 Chylothorax HSDN C2096293 Ent surgical result ear vertigo C0036439 Scoliosis, unspecified HSDN C2911647 Weight gain adverse event C0524851 Neurodegenerative disorders HSDN C0020538 Hbp C0009207 Cockayne syndrome OrphaNet|MalaCards C0522224 Palsied C0027746 Nerve degeneration HSDN C4084774 Have weight loss C0039006 Swine--diseases HSDN C3163620 Hypotension adverse event C3536715 Aa amyloidosis MalaCards C2024878 Cardiovascular surgery result: dyspnea C0243026 Sepsis HSDN C2036493 Stuttering characterized by prolongations C0038506 Stuttering UMLS C3887638 Failure to thrive in infant C0028758 Bonding HSDN C0003962 Ascites C0021071 Immunoproliferative small intestinal disease MalaCards C0013421 Dystonia C0024115 Lung diseases HSDN C0009676 Confusion state C3244301 Coverage level - family HSDN C0030193 Sense of pain C0024899 Mastocytosis HSDN C0042024 Urine incontinence C4041080 Neurocognitive disorders HSDN C0035229 Respiratory function impaired C0265354 Charge syndrome MalaCards|HPO C0007859 Pain neck C0020538 Hypertensive disease HSDN|UMLS C2096293 Ent surgical result ear vertigo C1546533 Specimen source codes - abscess HSDN C0000727 Abdomen acute C0021400 Influenza HSDN C0497406 Over weight C0031117 Peripheral neuropathy HSDN C0522224 Palsied C0035436 Rheumatic fever HSDN C3887638 Failure to thrive in infant C0033770 Prune belly syndrome MalaCards|HPO C1963086 Confusion adverse event C0032285 Pneumonia HSDN C0030193 Sense of pain C0027822 Neurodermatitis HSDN C0032617 High urine output C0022661 Kidney failure, chronic HSDN C1963091 Diarrhea adverse event C0031069 Familial mediterranean fever OrphaNet|HPO C0518090 Frequency of pain question C0036429 Sclerosis HSDN C0043094 Weight gain C0027697 Nephritis HSDN C0019079 Bloody sputum C0854975 Metastatic adenosquamous cell carcinoma of lung UMLS C0003862 Pain joint C1834304 Amyotrophy, hereditary neuralgic MalaCards C2242996 Tingling C0007784 Cerebral hemisphere hemorrhage HSDN C0015672 Decreased energy C0027073 Myofascial pain syndromes HSDN C0018775 Hearing loss bilateral C0022890 Labyrinthine disorder HSDN C0013421 Dystonia C0007222 Cardiovascular diseases HSDN C4084784 Diarrhea C0003175 Anthrax disease HSDN C3274924 Have been coughing C1546533 Specimen source codes - abscess HSDN C2315100 Pediatric failure to thrive C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C1963170 Hypothermia adverse event C0025289 Meningitis HSDN C0002962 Angina C0042344 Varicose ulcer HSDN C4084776 Weight loss C0002395 Alzheimer's disease HSDN C0013404 Respiratory difficulty C0042345 Varicosity HSDN C0019209 Large liver C0023806 Lipomucopolysaccharidosis HPO C0030552 Paralysis partial C0311284 Histiocytoma, giant cell MalaCards C1384666 Decreased hearing C4014939 Hennekam lymphangiectasia-lymphedema syndrome 2 MalaCards C3274924 Have been coughing C0023240 Legionellosis OrphaNet|MalaCards C0036572 Convulsion C3494975 Epileptic absence status, non-refractory UMLS C0518090 Frequency of pain question C4085635 Appetite quality question HSDN C1557397 Adverse event associated with pain C1384665 Hfe gene HSDN C0009806 Constipate C0268407 Senile cardiac amyloidosis MalaCards C3539896 Pelvic pain occurs with urination C0025202 Melanoma HSDN C4084774 Have weight loss C0021400 Influenza HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0752140 Intracranial embolism HSDN C4084727 Cough frequency C0520757 Delayed emergence from anesthesia HSDN C1963091 Diarrhea adverse event C0010074 Coronary vessel anomalies HSDN C1963137 Hydrocephalus adverse event C0003708 Arachnitis MalaCards C4085317 Diarrhea frequency C0029443 Osteomyelitis HSDN C4084725 Usual severity cough C0859897 Cord dysfunction vocal HSDN C0015469 Facial paralysis C0003615 Appendicitis HSDN C0518090 Frequency of pain question C0026705 Mucopolysaccharidosis ii HSDN C0042963 Symptoms vomiting C0376670 Pancreatitis, alcoholic UMLS C0037771 Paraparesis spastic C0019625 Sinus histiocytosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020876 Ileal neoplasms HSDN C0042928 Paralysis vocal cord C0007873 Uterine cervical neoplasm HSDN C1963252 Tremor adverse event C1837396 Congenital disorder of glycosylation, type ie MalaCards|HPO C1963087 Constipation adverse event C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0019825 Voice hoarseness C0268225 Aspartylglucosaminuria MalaCards|HPO|UMLS C1963281 Vomiting adverse event C0035400 Reyes syndrome HSDN C4084784 Diarrhea C0041374 Tumor virus infections HSDN C4084784 Diarrhea C0031873 Pica disease HSDN C0007398 Catatonic C0439840 Reflex motion descriptor HSDN C0018784 Deafness sensorineural C0265554 Ectrodactyly MalaCards|HPO C4084767 Bothered by vomiting C0011981 Diaphragmatic eventration HSDN C0234146 Absent reflex C3539003 Neuropathy, hereditary sensory and autonomic, type vi MalaCards C0010200 Cough symptom C0027627 Neoplasm metastasis HSDN C1963093 Dizziness adverse event C0005967 Bone neoplasms HSDN C0037316 Not enough sleeping C0027051 Myocardial infarction HSDN C4084769 Vomiting frequency C0025297 Viral meningitis HSDN C3641756 Have diarrhea C0004030 Aspergillosis HSDN C3541349 Syncope C0002895 Anemia, sickle cell HSDN C0042963 Symptoms vomiting C0027430 Nasal polyps HSDN C4085222 Nausea C0008370 Cholestasis HSDN C0028738 Nystagmus C2931386 Amaurosis congenita of leber, 3 MalaCards C4084775 Usual severity weight loss C0023470 Myeloid leukemia HSDN C0023015 Language handicap C0009651 Conditioning operant HSDN C0013421 Dystonia C0036202 Sarcoidosis HSDN C0042963 Symptoms vomiting C0151740 Intracranial hypertension HSDN C0009806 Constipate C1000483 Genus anemia HSDN C0015469 Facial paralysis C0007772 Intracranial arteriovenous malformation HSDN C4084723 Constipation C0003873 Rheumatoid arthritis HSDN C2203646 Jaundice C0342859 Harderoporphyria HPO C4084726 Distress cough C0012644 Animal disease models HSDN C3887873 Hearing loss C0029422 Osteochondrodysplasias HSDN C0019209 Large liver C1306220 Fort bragg fever MalaCards C0878773 Bladder hyperactive C0453996 Tobacco smoking HSDN C4042891 Sleep wake disorders C0453996 Tobacco smoking HSDN C3641755 Have constipation C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0242936 Center pain C0017919 Glycogen storage disease HSDN C0036572 Convulsion C0265493 Cat eye syndrome MalaCards C2984058 Have pain C0016658 Fracture bone HSDN C0002170 Alopecia disorders C0406612 Encephalocraniocutaneous lipomatosis OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0022568 Keratitis HSDN C0043094 Weight gain C0014394 Enuresis HSDN C4085317 Diarrhea frequency C0020619 Hypogonadism HSDN C2237041 Shox gene with short stature C0410180 Eichsfeld type congenital muscular dystrophy HPO C1069915 Vertigo C0019562 Von hippel-lindau syndrome MalaCards|HSDN|HPO C4085210 Usual severity pain C1963234 Serum sickness adverse event HSDN C0015672 Decreased energy C0011633 Dermatomyositis OrphaNet|MalaCards C0423823 Nail thinness C0220765 Weaver-like syndrome MalaCards|HPO C2911645 Weight loss adverse event C0027743 Nerve compression syndrome HSDN C0010200 Cough symptom C0042133 Uterine fibroids HSDN C3815497 Cough C0009324 Ulcerative colitis HSDN C0018524 Hallucinate C0012979 Canine disease HSDN C1963180 Neck pain adverse event C0086957 Naffziger syndrome HSDN C0008031 Pain chest C1708955 Mediastinal malignant germ cell tumor with associated hematologic malignancy UMLS C2881384 Sudden visual loss, left eye C0809996 Blindness and vision defects UMLS C0000737 Abdomen pain C1332254 Ampulla of vater undifferentiated carcinoma UMLS C0019825 Voice hoarseness C0460137 Push down or depress HSDN C3898969 Have been vomiting C0007932 Chagas' disease + no organ inv DiseaseOntology C0043094 Weight gain C0001584 Adolescent psychology HSDN C0151686 Growth retardation C3553571 Congenital disorder of glycosylation, type iik MalaCards C2024893 Cardiovascular surgery result: fatigue C1527348 Brain hypoxia HSDN C2203646 Jaundice C1096660 Ehlers-danlos syndrome type ix MalaCards C3541349 Syncope C0027663 Neoplasms, multiple primary HSDN C1963281 Vomiting adverse event C0036864 Sexual relations HSDN C0000727 Abdomen acute C0021359 Infertility HSDN C0000737 Abdomen pain C0033860 Psoriasis HSDN C3539896 Pelvic pain occurs with urination C0014179 Endometritis HSDN C0013604 Edematous C4085635 Appetite quality question HSDN C0011991 Loose stools C0004239 Atrial flutter HSDN C0003962 Ascites C0023806 Lipomucopolysaccharidosis HPO C0349588 Stature short C0015625 Fanconi anemia OrphaNet|HPO|MalaCards C0454644 Delayed language development C0035934 Rubinstein-taybi syndrome HPO C0000727 Abdomen acute C0025286 Meningioma HSDN C4084774 Have weight loss C2984572 Malaria pathway HSDN C0011168 Disorder deglutition C2750537 Myopathy, actin, congenital, with cores HPO C1565249 Limitation, mobility C1999266 Depression adverse event HSDN C2188196 Unreasonable fears with compelling desire to avoid C1609481 Hydrophobia UMLS C0007758 Cerebellar ataxia C0270611 Brain damage HSDN C2984058 Have pain C0038987 Sweat gland neoplasms HSDN C0009763 Conjunctiva inflammation C3840167 Acute coccidioidomycosis MalaCards C0344435 Ventricular fibrillation by ecg finding C0035828 Romano-ward syndrome MalaCards|HPO C0007758 Cerebellar ataxia C0270750 Cerebellar ataxia, sanger-brown UMLS C0349588 Stature short C1859252 Cerebrofaciothoracic dysplasia OrphaNet|HPO|MalaCards C0033774 Skin pruritus C0263343 Urticaria pigmentosa, multiple nodules or plaques UMLS C1959630 Eye pain adverse event C0015414 Eye neoplasms HSDN C3898969 Have been vomiting C0027430 Nasal polyps HSDN C0009806 Constipate C1333870 Grade 1 rectal adenocarcinoma UMLS C4084767 Bothered by vomiting C0085389 Bacillaceae infection HSDN C0024031 Back pain lower back C0003486 Aortic aneurysm HSDN C0022346 Yellow skin C0032966 Complication, neoplastic pregnancy HSDN C0009806 Constipate C0036421 Systemic scleroderma HSDN C0019209 Large liver C3810325 Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis MalaCards C4084802 Usual severity diarrhea C0034063 Pulmonary edema HSDN C0239574 Fever low grade C0149725 Lower respiratory tract infection MalaCards C4084774 Have weight loss C0038663 Suicide attempt HSDN C0745966 Lower leg edema C0033103 Pretibial myxedema UMLS C0033774 Skin pruritus C0015802 Femur fracture HSDN C0007166 Cardiac output decreased C0812393 Cancer patients and suicide and depression HSDN C3898969 Have been vomiting C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C3274924 Have been coughing C2984572 Malaria pathway HSDN C0028738 Nystagmus C3542026 Peroxisome biogenesis disorder 5b MalaCards C0018784 Deafness sensorineural C0002874 Aplastic anemia HSDN C0030193 Sense of pain C0003618 Appetites HSDN C4084767 Bothered by vomiting C0024919 Behavior, maternal HSDN C0004604 Pain back C0003838 Arterial occlusive diseases HSDN C0518090 Frequency of pain question C0010631 Cystadenocarcinoma HSDN C0008031 Pain chest C0232347 No-reflow phenomenon HSDN C0003460 Anurias C2678367 Renal tubular dysgenesis with choanal atresia and athelia HPO C3463815 Feel fatigue C3178770 Nutcracker syndrome, renal HSDN C0026603 Motion sickness C0453996 Tobacco smoking HSDN C0018681 Headache, cephalalgia C0023434 Chronic lymphocytic leukemia HSDN C0917816 Deficiency mental C3540845 Microphthalmia, isolated, with coloboma 8 MalaCards C0522179 Anxiety death C0349231 Phobic anxiety disorder UMLS C0030200 Intractable pain C1258104 Diffuse scleroderma HSDN C4084725 Usual severity cough C0020541 Hypertension, portal HSDN C0026838 Spasticity muscle C0027819 Neuroblastoma HSDN C0002622 Amnesias C0342257 Complications of diabetes mellitus HSDN C4084723 Constipation C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO C0162298 Stiffness joints C0795933 Edinburgh malformation syndrome MalaCards C0025874 Uterine bleeding dysfunctional C0524541 Deciduoma MalaCards C0035078 Failure kidney C1510460 Orofaciodigital syndrome i MalaCards|HPO C1069915 Vertigo C1707400 Classic medulloblastoma MalaCards C0012833 Dizzy C0010964 Dandy-walker syndrome HSDN C1963091 Diarrhea adverse event C0162531 Hereditary coproporphyria HPO C3274924 Have been coughing C0023267 Fibroid tumor HSDN C3539020 Pelvic pain decreasing in frequency C0004936 Mental disorders HSDN C0019079 Bloody sputum C1707407 Clear cell carcinoma of lung, large cell type UMLS C0151786 Weakness muscle C0751357 Focal myositides MalaCards C4084767 Bothered by vomiting C0037856 Spermatic cord torsion HSDN C4084774 Have weight loss C0029410 Osteoarthritis of hip HSDN C4084784 Diarrhea C0003090 Ankylosis HSDN C0018834 Brash C0028860 Oculocerebrorenal syndrome HPO C4084775 Usual severity weight loss C0025427 Mercury poisoning HSDN C0018681 Headache, cephalalgia C0004763 Barrett esophagus HSDN C0878773 Bladder hyperactive C1956346 Coronary artery disease HSDN C0037316 Not enough sleeping C3163620 Hypotension adverse event HSDN C1142421 Adnexa uteri tenderness C1142117 Adnexa uteri pain UMLS C0860603 Anxiety symptom C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0344315 Mood depressed C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C3887638 Failure to thrive in infant C0028860 Oculocerebrorenal syndrome OrphaNet|HSDN|HPO C0011206 Delirium acute C0023066 Laryngismus HSDN C4084788 Have dizziness C0860603 Anxiety symptoms HSDN C1963093 Dizziness adverse event C0796561 Melanoma vaccines HSDN C4085210 Usual severity pain C0001815 Primary myelofibrosis HSDN C4084775 Usual severity weight loss C0002871 Anemia HSDN C0005745 Blepharoptosis C0265220 Pallister-hall syndrome MalaCards C0152459 Striae C0347555 Friction blister HSDN C1549543 Administration method - pain C1510428 Cerebral abscess HSDN C0030193 Sense of pain C0334384 Infiltrating duct and lobular carcinoma UMLS C0000786 Abortion spontaneous C0043398 Yellow fever, urban MalaCards C0424755 Fever symptoms C0162871 Aortic aneurysm, abdominal HSDN C0008031 Pain chest C0024525 Malacoplakia MalaCards C3541349 Syncope C1963198 Pancreatitis adverse event HSDN C3898969 Have been vomiting C1261128 Progeria-like syndrome MalaCards C2919142 Short stature adverse event C3278138 Fibrochondrogenesis 1 MalaCards C2919142 Short stature adverse event C3150803 Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia MalaCards|HPO C3887873 Hearing loss C0019562 Von hippel-lindau syndrome HSDN C4084726 Distress cough C0013274 Patent ductus arteriosus HSDN C0000731 Abdomen distention C0749420 Thyroid agenesis HPO C3641755 Have constipation C0019326 Ventral hernia HSDN C0019209 Large liver C0432219 Opsismodysplasia MalaCards|HPO C4084897 Sleep disturbance subordinate domain C2931542 Shapiro syndrome OrphaNet|MalaCards C0242936 Center pain C0037355 Smallpox vaccines HSDN C0270948 Neurogenic muscular atrophy C4015452 Polyglucosan body myopathy 2 MalaCards C0022346 Yellow skin C2015933 Outcomes otolaryngology hearing HSDN C3665347 Vision impaired C2930852 Zellweger leukodystrophy MalaCards C0030552 Paralysis partial C0023473 Myeloid leukemia, chronic HSDN C0002622 Amnesias C0085632 Apathy HSDN C3641756 Have diarrhea C0009244 Behavioral cognitive therapy HSDN C0032617 High urine output C0085258 Deficiency, yang HSDN C0036572 Convulsion C0022660 Kidney failure, acute HSDN C0242936 Center pain C0206762 Limb deformities, congenital HSDN C0151889 Reflexes tendon increased C2750536 Nemaline myopathy 3, with intranuclear rods HPO C4085210 Usual severity pain C0006262 Bronchial fistula HSDN C0030193 Sense of pain C0020461 Hyperkalemia HSDN C0497406 Over weight C0033348 Language program HSDN C0010200 Cough symptom C1266036 Indeterminate bronchioloalveolar carcinoma UMLS C4084788 Have dizziness C0001584 Adolescent psychology HSDN C0007814 Cerebrospinal fluid otorrhea C0751814 Brain injuries, vascular HSDN C2024878 Cardiovascular surgery result: dyspnea C0016977 Gall bladder diseases HSDN C1963281 Vomiting adverse event C0376547 Aromatherapy HSDN C0042928 Paralysis vocal cord C2937358 Cerebral hemorrhage HSDN C0013404 Respiratory difficulty C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C3150953 Long qt syndrome 6 MalaCards|HPO C0749874 Upper respiratory symptom C0740767 Resp_tract problem UMLS C1549543 Administration method - pain C0016995 Gambling HSDN C0018926 Emesis bloody C0001815 Primary myelofibrosis HSDN C0030975 Disorders perception C0018790 Cardiac arrest HSDN C0042963 Symptoms vomiting C1962958 Hematoma adverse event HSDN C0030193 Sense of pain C0392525 Nephrolithiasis HSDN C0750426 Wbc elevated C1327918 Oculootoradial syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0001486 Adenovirus infections HSDN C0011991 Loose stools C0042133 Uterine fibroids HSDN C3539893 Pelvic pain occurs with intercourse C0520676 Premenstrual dysphoric disorder HSDN C3641755 Have constipation C0003493 Aortic diseases HSDN C2237041 Shox gene with short stature C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C0042571 Vertigo subjective C0026650 Movement disorders HSDN C4084768 Usual severity vomiting C0003486 Aortic aneurysm HSDN C1145670 Failure respiratory C0158641 Lung, cysts, congenital MalaCards C0000737 Abdomen pain C0030767 Grouping peer HSDN C0751900 Motor tic C0018523 Hallervorden-spatz syndrome MalaCards|HPO|UMLS C0018772 Deafness C3697269 15q24 microdeletion OrphaNet|HPO C0027796 Neuralgias C0033893 Tension headache HSDN C0151889 Reflexes tendon increased C1855255 Pseudoarylsulfatase a deficiency MalaCards|HPO C2203646 Jaundice C0019189 Hepatitis, chronic HSDN C2237041 Shox gene with short stature C3809007 Cardiofaciocutaneous syndrome 4 MalaCards C3887638 Failure to thrive in infant C0275859 Syphilis, congenital, early MalaCards C0007758 Cerebellar ataxia C0338430 Limbic encephalitis HSDN C4042891 Sleep wake disorders C0011127 Pressure ulcer HSDN C1963087 Constipation adverse event C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0221170 Stiffness muscle C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C4084768 Usual severity vomiting C0497327 Dementia HSDN C4084767 Bothered by vomiting C1548777 Specimen reject reason - hemolysis HSDN C3539020 Pelvic pain decreasing in frequency C0206767 Neoplasms, cystic, mucinous, and serous HSDN C0023014 Developmental disorder language C0162532 Variegate porphyria HSDN C2032395 Pelvic pain on the left C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C3274924 Have been coughing C0033036 Atrial premature complexes HSDN C0002962 Angina C0342881 Familial hypercholesterolemia - homozygous OrphaNet|HPO|MalaCards C0028738 Nystagmus C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C1557397 Adverse event associated with pain C0085315 Toxoplasmosis, cerebral HSDN C0009421 Comatose C4042784 Feeding and eating disorders HSDN C0003962 Ascites C2931360 Weber klippel trenaunay MalaCards C2911647 Weight gain adverse event C0014547 Epilepsies, partial HSDN C1963063 Anorexia adverse event C0039841 Thiamine deficiency HSDN C0018926 Emesis bloody C0018552 Hamartoma HSDN C0018772 Deafness C0018800 Cardiomegaly HSDN C1963093 Dizziness adverse event C0020502 Hyperparathyroidism HSDN C0002170 Alopecia disorders C0040250 Tinea capitis MalaCards C1962956 Flatulence adverse event C0009324 Ulcerative colitis HSDN C0009806 Constipate C3280479 Pitt-hopkins-like syndrome 2 MalaCards|UMLS C1961131 Cough adverse event C0032319 Pneumopericardium HSDN C0013604 Edematous C0029944 Drug overdose HSDN C2911645 Weight loss adverse event C0023903 Liver neoplasms MalaCards C0018681 Headache, cephalalgia C0242339 Dyslipidemias HSDN C0009460 Communication impairment C0079631 Interdisciplinary communication HSDN C4084726 Distress cough C0024788 Green monkey virus disease OrphaNet|MalaCards C4085210 Usual severity pain C1253937 Pericardial effusion HSDN C0043094 Weight gain C0018188 Granuloma HSDN C2911645 Weight loss adverse event C0206042 Fatal familial insomnia HPO C0020673 Hypothermia (central) (local) C0005891 Bodies image HSDN C4085211 Pain distress question C0035459 Atrophic rhinitis HSDN C4085222 Nausea C0036864 Sexual relations HSDN C3887638 Failure to thrive in infant C1836669 Congenital disorder of glycosylation, type if MalaCards|HPO C0019521 Hiccoughs C0021890 Intraoperative complications HSDN C4084727 Cough frequency C0018800 Cardiomegaly HSDN C0015970 Fever unknown origin C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1557397 Adverse event associated with pain C0235146 Emotionally high HSDN C4084723 Constipation C0032962 Pregnancy complications HSDN C1963170 Hypothermia adverse event C0038358 Gastric ulcer HSDN C4084768 Usual severity vomiting C0029134 Optic neuritis HSDN C0043094 Weight gain C0162316 Iron deficiency anemia HSDN C2242996 Tingling C2936881 Eosinophilic synovitis MalaCards C0018681 Headache, cephalalgia C0013808 Electroconvulsive therapy HSDN C2024893 Cardiovascular surgery result: fatigue C0007762 Cerebellar neoplasms HSDN C4084788 Have dizziness C0035304 Retinal degeneration HSDN C0030193 Sense of pain C0275148 Poisoning of animal by plant HSDN C0040264 Ear ringing sound C1522133 High cholesterol level HSDN C4085317 Diarrhea frequency C0022548 Keloid HSDN C4085210 Usual severity pain C0024523 Malabsorption syndrome HSDN C0013404 Respiratory difficulty C0305062 Tetanus toxoids HSDN C1384666 Decreased hearing C0023473 Myeloid leukemia, chronic HSDN C0424755 Fever symptoms C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C4085211 Pain distress question C0020564 Hypertrophy HSDN C2010791 Generalized lesions excluding the palms and soles which feel like sandpaper C0037284 Skin lesion UMLS C0349588 Stature short C1837481 Spondyloepimetaphyseal dysplasia, matrilin-3 related OrphaNet C3898969 Have been vomiting C0016952 Galactosemias MalaCards C4085211 Pain distress question C0040761 Transposition of great vessels HSDN C3887873 Hearing loss C0032460 Polycystic ovary syndrome HSDN C0151786 Weakness muscle C0037274 Dermatologic disorders HSDN C4084802 Usual severity diarrhea C0007273 Carotid artery diseases HSDN C3539023 Pelvic pain increasing in frequency C1546847 Entity name part type - family HSDN C2911647 Weight gain adverse event C0035235 Respiratory syncytial virus infections HSDN C1963091 Diarrhea adverse event C2004491 Cicatrix HSDN C2237041 Shox gene with short stature C2936816 Micromelic dysplasia, congenital, with dislocation of radius MalaCards C0008031 Pain chest C0684249 Carcinoma of lung UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C2355609 Mycetoma of foot HSDN C2984058 Have pain C0024667 Animal mammary neoplasms HSDN C0231528 Muscle pain generalized C2931743 Lactate dehydrogenase deficiency type a MalaCards|UMLS C1557397 Adverse event associated with pain C0600040 Chronic interstitial cystitis OrphaNet C0243026 Generalized infection C0043194 Wiskott-aldrich syndrome MalaCards|HPO C1963093 Dizziness adverse event C0017612 Glaucoma, open-angle HSDN C0349588 Stature short C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0423773 Skin scaly C2749659 Aicardi-goutieres syndrome 5 (disorder) MalaCards C4084784 Diarrhea C0853698 Lymphocytes increased HSDN C0031911 Pigment deposition C0241989 Malignant melanoma of vulva MalaCards C1557397 Adverse event associated with pain C0003892 Neurogenic arthropathy HSDN C1971624 Appetite absent C0018799 Heart diseases HSDN C0231531 Fibrillation muscle C1720189 Episodic ataxia MalaCards C0024902 Mastodynia C0017653 Glomus tumor HSDN C0020673 Hypothermia (central) (local) C0022638 Ketosis HSDN C4084766 Vomiting C1261128 Progeria-like syndrome MalaCards C0015230 Exanthem C0570577 Ranitidine allergy UMLS C1963184 Nystagmus adverse event C1868576 Paroxysmal tonic upgaze, benign childhood, with ataxia OrphaNet|MalaCards C0036572 Convulsion C2931296 Yorifuji okuno syndrome HPO C0013404 Respiratory difficulty C1956415 Paroxysmal nocturnal dyspnea UMLS C4084768 Usual severity vomiting C0031269 Peutz-jeghers syndrome MalaCards|HSDN|HPO C2984058 Have pain C0024205 Lymphadenitis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0002395 Alzheimer's disease HSDN C4085211 Pain distress question C0013336 Dwarfism HSDN C0030193 Sense of pain C0009326 Collagen diseases HSDN C1319542 On examination - left eye proliferative diabetic retinopathy C0011164 Abnormal degeneration UMLS C0020538 Hbp C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C3641756 Have diarrhea C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C0008031 Pain chest C0014461 Granuloma eosinophilic MalaCards C0018772 Deafness C0025284 Meningeal neoplasms HSDN C0039070 Collapse fleeting C0033871 Psychiatric status rating scales HSDN C1549543 Administration method - pain C0038363 Aphthous stomatitis HSDN C0036659 Sensation disorder C1720777 Functional laterality HSDN C0004310 Auditory disorder process C0038186 Reflex, startle HSDN C0038506 Stutter C0022701 Kinesthesia HSDN C4084767 Bothered by vomiting C1856405 Glutaric aciduria iic HPO C2984058 Have pain C0035235 Respiratory syncytial virus infections HSDN C2165316 Delusions that one's body is infested with parasites C0011253 Delusions UMLS C0029163 Hemorrhage mouth C0036093 Salivary gland diseases HSDN C0000737 Abdomen pain C0000810 Incomplete spontaneous abortion HSDN C0424755 Fever symptoms C0040038 Thromboembolism HSDN C3829611 Nausea frequency C2963140 Arteriovenous fistula in use with two needles HSDN C0000737 Abdomen pain C0240812 Pain prostatic UMLS C4084774 Have weight loss C0007124 Noninfiltrating intraductal carcinoma HSDN C4084776 Weight loss C0233629 Thinking and speaking disturbances HSDN C0015469 Facial paralysis C0036439 Scoliosis, unspecified HSDN C0011991 Loose stools C1145670 Respiratory failure HSDN C0042798 Vision dim C3150819 Retinitis pigmentosa 56 MalaCards|HPO C0011991 Loose stools C0019557 Hip fx HSDN C0151889 Reflexes tendon increased C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C4085211 Pain distress question C0206644 Histiocytoma, benign fibrous HSDN C0233514 Behavior abnormal C0035372 Rett syndrome OrphaNet|MalaCards C0036396 Sciatica C0282606 Myomatous neoplasm HSDN C0023014 Developmental disorder language C0017178 Gastrointestinal diseases HSDN C0015672 Decreased energy C0038012 Spondylitis HSDN C3641755 Have constipation C0017638 Glioma HSDN C0018681 Headache, cephalalgia C1332865 Cavernous sinus meningioma UMLS C3887638 Failure to thrive in infant C3150750 Agammaglobulinemia 2, autosomal recessive MalaCards C0009421 Comatose C0017658 Glomerulonephritis HSDN C0020649 Blood pressure decreased C0043397 Yellow fever, jungle MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0029295 Oropharyngeal neoplasms HSDN C4085210 Usual severity pain C1547044 Kind of quantity - smell HSDN C0030193 Sense of pain C0032797 Postpartum hemorrhage HSDN C0015469 Facial paralysis C1869123 Limb-girdle muscular dystrophy type 2a MalaCards|HPO C0009421 Comatose C0020461 Hyperkalemia HSDN C0002624 Amnesia retrograde C0024121 Lung neoplasms HSDN C3887638 Failure to thrive in infant C2931296 Yorifuji okuno syndrome OrphaNet|HPO C4084775 Usual severity weight loss C0035066 Renal artery obstruction HSDN C0018681 Headache, cephalalgia C1832033 Adult subependymal giant cell astrocytoma UMLS C0012833 Dizzy C2984299 Asthma pathway HSDN C2203646 Jaundice C0027145 Myxedema HSDN C0030552 Paralysis partial C0017636 Glioblastoma MalaCards|HSDN C3898969 Have been vomiting C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0241157 Skin pustule C4015130 Inflammatory skin and bowel disease, neonatal, 2 MalaCards C1963087 Constipation adverse event C0038356 Stomach neoplasms HSDN C0036572 Convulsion C1833538 Orofacial cleft 7 MalaCards C0231218 Malaise generalized C1332249 Ampulla of vater signet ring cell carcinoma UMLS C0018926 Emesis bloody C0008325 Cholecystitis HSDN C0018772 Deafness C0039494 Temporomandibular joint disorders HSDN C3641756 Have diarrhea C0029001 Onchocerciasis HSDN C0013604 Edematous C0085183 Neoplasms, second primary HSDN C0332563 Papulae C0023648 Lichen planus, bullous OrphaNet|MalaCards C0042963 Symptoms vomiting C1857728 Hereditary angioedema type iii MalaCards|HPO C0036572 Convulsion C3662031 Intractable absence seizures UMLS C3641756 Have diarrhea C0004610 Bacteremia HSDN C0018784 Deafness sensorineural C0006112 Brain diseases, metabolic HSDN C0018524 Hallucinate C2984572 Malaria pathway HSDN C0030193 Sense of pain C0022336 Creutzfeldt-jakob disease HSDN C4085210 Usual severity pain C0016507 Acquired foot deformities HSDN C0857305 Thrombocytopenia purpura C0041331 Splenic tuberculoses HSDN C0851578 Disorder sleep C0022116 Ischemia HSDN C1838869 Proximal neurogenic muscle weakness C1848029 Ehlers-danlos syndrome caused by tenascin-x deficiency OrphaNet|HPO C4082202 Sleep quality question C0948264 Neuroborreliosis MalaCards C3463815 Feel fatigue C2973725 Pulmonary arterial hypertension OrphaNet C0577567 Mass of urogenital structure C0519067 Renal interstitial sarcoidosis UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C2350530 Bronchopulmonary aspergillosis HSDN C3463815 Feel fatigue C0043325 Xanthomatosis HSDN C0004604 Pain back C0032371 Poliomyelitis HSDN C0349588 Stature short C2931720 Fronto-facio-nasal dysostosis OrphaNet|MalaCards C0027498 Nausea vomiting C0085083 Ovarian hyperstimulation syndrome OrphaNet|MalaCards C0019209 Large liver C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C0162285 Edema eyelid C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C4084768 Usual severity vomiting C0020456 Hyperglycemia HSDN C0022346 Yellow skin C0700095 Central neuroblastoma HSDN C0013595 Eczematous dermatitis C0349426 Ferrochelatase deficiency HPO C4084725 Usual severity cough C1455705 Pulmonary histiocytosis x OrphaNet|MalaCards C0012833 Dizzy C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards C4084726 Distress cough C0348018 Projections HSDN C2096293 Ent surgical result ear vertigo C0004238 Atrial fibrillation HSDN C0036572 Convulsion C3281084 Congenital disorder of glycosylation, type ir MalaCards C0242936 Center pain C0019034 Hemoglobin sc disease MalaCards|HSDN C4084723 Constipation C0029106 Opisthorchiasis DiseaseOntology C0030193 Sense of pain C0027746 Nerve degeneration HSDN C2203646 Jaundice C0268608 Deficiency of dihydrofolate reductase MalaCards C0751837 Gait ataxic C0021432 Infratentorial neoplasms HSDN C2237041 Shox gene with short stature C1846058 Lubs x-linked mental retardation syndrome OrphaNet|HPO C0033774 Skin pruritus C1963067 Atrial fibrillation adverse event HSDN C0018991 Paralysis one side of body C0153259 Meningitis coccidioidal UMLS C0878638 Tongue signs C0796280 Acromegaloid facial appearance syndrome OrphaNet|MalaCards C0018772 Deafness C1959582 Pten hamartoma tumor syndrome MalaCards C4085211 Pain distress question C0011880 Diabetic ketoacidosis HSDN C0030486 Extremity paralysis, lower C2931355 Spastic paraplegia 3, autosomal dominant OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C0024630 Malingering HSDN C0344232 Blurred vision C1836148 Supranuclear palsy, progressive, 2 MalaCards|UMLS C2096293 Ent surgical result ear vertigo C0037929 Spinal cord injuries HSDN C4084725 Usual severity cough C0007133 Carcinoma, papillary HSDN C0030193 Sense of pain C0035078 Kidney failure HSDN C0018772 Deafness C1866927 Smcr HPO C4085211 Pain distress question C0004044 Asphyxia HSDN C0043094 Weight gain C0031090 Periodontal diseases HSDN C0013394 Coitus painful C1720830 Painful bladder syndrome OrphaNet|MalaCards C1510417 Apraxia of gait C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0727671 Red cross toothache drops C0043049 Water intoxication HSDN C4084766 Vomiting C0032851 Disease poultry HSDN C1961131 Cough adverse event C0015745 Ingestive behavior HSDN C0028961 Urine output decreased C2239253 Aneurysm of sinus of valsalva MalaCards C0030193 Sense of pain C1546747 Specimen source codes - polyps HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0026857 Musculoskeletal diseases HSDN C4084726 Distress cough C1535939 Pneumocystis jiroveci pneumonia HSDN C4085549 Dizziness C0085541 Epilepsy, frontal lobe HSDN C0018681 Headache, cephalalgia C0035229 Respiratory insufficiency HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0560651 Spinal cord syndrome central HSDN C1557397 Adverse event associated with pain C0035439 Rheumatic heart disease HSDN C3898969 Have been vomiting C0268410 Acid phosphatase deficiency HPO C4020887 Photodysphoria C0220701 Retinitis pigmentosa 1 MalaCards C0019209 Large liver C1833541 Caroli disease isolated MalaCards C4084767 Bothered by vomiting C1275081 Cardio-facio-cutaneous syndrome HPO C0034150 Skin purpura C0001973 Alcoholic intoxication, chronic HSDN C0085602 Polydypsia C0035410 Rhabdomyolysis HSDN C2984058 Have pain C1384665 Hfe gene HSDN C0007758 Cerebellar ataxia C3553937 Pbd4b MalaCards C4085211 Pain distress question C0007867 Cervix diseases HSDN C2936821 Spinal cerebrospinal fluid leak C0017671 Glomus jugulare tumor HSDN C0036572 Convulsion C0027947 Neutropenia HSDN C1963090 Dehydration adverse event C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards|HPO C1963093 Dizziness adverse event C0155490 Middle ear cholesteatoma HSDN C2911647 Weight gain adverse event C0033860 Psoriasis HSDN C0231528 Muscle pain generalized C0029429 Osteochondrosis HSDN C4085210 Usual severity pain C0025290 Aseptic meningitis HSDN C0030554 Abnormal sensation C0268322 Chester-type porphyria HPO C0015672 Decreased energy C1963274 Vasculitis adverse event HSDN C1962972 Proteinuria adverse event C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C4084725 Usual severity cough C0023092 Lassa fever OrphaNet|MalaCards C0023015 Language handicap C0033962 Psychosocial deprivation HSDN C4084769 Vomiting frequency C0017185 Gastrointestinal neoplasms HSDN C0392699 Dysaesthesia C0751549 Neurogenic thoracic outlet syndrome OrphaNet|MalaCards C4085222 Nausea C0034194 Pyloric stenosis HSDN C1963184 Nystagmus adverse event C2931226 Thompson baraitser syndrome OrphaNet|MalaCards C0036659 Sensation disorder C1704770 Nci thesaurus association HSDN C0424755 Fever symptoms C1304205 Neutrophilic urticaria MalaCards C0751495 Seizure focal C0278188 Seizure visual UMLS C4042891 Sleep wake disorders C0011334 Dental caries HSDN C1963063 Anorexia adverse event C0011168 Deglutition disorders HSDN C0009676 Confusion state C1963090 Dehydration adverse event HSDN C3463815 Feel fatigue C0206171 Community acquired infections HSDN C0020438 Hypercalciuria C0020630 Hypophosphatasia HSDN C0020538 Hbp C0542519 Congenital absence of kidney MalaCards C4084723 Constipation C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1955864 Cardiac sinus arrest HSDN C0009806 Constipate C0027947 Neutropenia HSDN C3829611 Nausea frequency C0017152 Gastritis HSDN C4085317 Diarrhea frequency C0016085 Filariasis HSDN C0241137 Skin pallor C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C0086439 Activity decreased C0004936 Mental disorders HSDN C0030193 Sense of pain C0001403 Addison disease HSDN C0019572 Hairiness C0795933 Edinburgh malformation syndrome OrphaNet|MalaCards C0000737 Abdomen pain C2749484 Neuroblastoma, susceptibility to HPO C4085862 Bothered by nausea C1552527 Clinic / center - developmental disabilities HSDN C0043352 Absent salivary secretion C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive OrphaNet|MalaCards C0027497 Queasy C1332254 Ampulla of vater undifferentiated carcinoma UMLS C1565249 Limitation, mobility C0007131 Non-small cell lung carcinoma HSDN C1963184 Nystagmus adverse event C3150315 Aicardi-goutieres syndrome 1, autosomal dominant HPO C1963170 Hypothermia adverse event C0342257 Complications of diabetes mellitus HSDN C4085661 Usual severity nausea C0011119 Decompression sickness HSDN C1963091 Diarrhea adverse event C0036262 Sarcoptic itch HSDN C0010520 Skin cyanosis C0334299 Carcinoid tumor no icd-o subtype HSDN C0011991 Loose stools C0009917 Contracture HSDN C2984057 Have nausea C0030286 Pancreatic diseases HSDN C0848203 Male pelvic pain C0037051 Behavior illness HSDN C0917816 Deficiency mental C0023374 Lesch-nyhan syndrome MalaCards|HPO C0026821 Cramp C0002994 Angioedema HSDN C4085549 Dizziness C2984572 Malaria pathway HSDN C1549543 Administration method - pain C0026918 Mycobacterium infections HSDN C4085317 Diarrhea frequency C0009244 Behavioral cognitive therapy HSDN C0009806 Constipate C0004935 Animal ethology HSDN C1856661 Cornea cloudy C1838329 Aplasia cutis congenita with epibulbar dermoids MalaCards C0020672 Body temperature decreased C0024141 Lupus erythematosus, systemic HSDN C0036572 Convulsion C0003431 Antisocial personality disorder HSDN C0003910 Articulation disorder C0022366 Jaw, edentulous HSDN C0004604 Pain back C0016171 Fistula of intestine, excluding rectum and anus HSDN C2919142 Short stature adverse event C4015067 Autoinflammation with infantile enterocolitis MalaCards C0020673 Hypothermia (central) (local) C0006663 Calcinosis HSDN C1963093 Dizziness adverse event C0011881 Diabetic nephropathy HSDN C0349588 Stature short C2931280 Congenital alopecia, psychomotor retardation, convulsions OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C0079683 Herlitz disease OrphaNet|HPO|MalaCards C0522224 Palsied C3813607 Infantile gastroesophageal reflux HSDN C0028738 Nystagmus C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C3665347 Vision impaired C1857779 Senior-loken syndrome 6 MalaCards|HPO C0018784 Deafness sensorineural C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0018772 Deafness C0040034 Thrombocytopenia HSDN C3641756 Have diarrhea C0271972 Thiamine-responsive megaloblastic anemia MalaCards C2911645 Weight loss adverse event C0034885 Rectal neoplasms HSDN C4085317 Diarrhea frequency C0020039 Hostility HSDN C0085649 Edema extremities C1850055 Peho syndrome OrphaNet|HPO|MalaCards C0040822 D tremors C1968552 Mental retardation, x-linked, with spasticity HPO C2919142 Short stature adverse event C1866994 Ulnar-mammary syndrome MalaCards C3887638 Failure to thrive in infant C0796147 Acrocallosal syndrome MalaCards|HPO C0036572 Convulsion C0853697 Neutrophil count decreased HSDN C0700078 Deep tendon reflex decrease C4015184 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 MalaCards C3146279 Coma C0039128 Syphilis HSDN C0857305 Thrombocytopenia purpura C0027765 Nervous system disorder HSDN C0030193 Sense of pain C0005639 Bisexual behavior HSDN C2024893 Cardiovascular surgery result: fatigue C0027627 Neoplasm metastasis HSDN C0020639 Hypoproteinaemia C1855796 Hypoproteinemia, hypercatabolic HPO C0518090 Frequency of pain question C0024809 Marijuana abuse HSDN C4084784 Diarrhea C0018944 Hematoma HSDN C0242936 Center pain C0036216 Sarcoma, experimental HSDN C2024878 Cardiovascular surgery result: dyspnea C1548777 Specimen reject reason - hemolysis HSDN C0027497 Queasy C0008313 Cholangitis, sclerosing UMLS C4085211 Pain distress question C0014100 Endarteritis, nos HSDN C0424755 Fever symptoms C0037421 Social isolation HSDN C4084788 Have dizziness C0023418 Leukemia HSDN C2096293 Ent surgical result ear vertigo C0340493 Paroxysmal familial ventricular fibrillation MalaCards C0009676 Confusion state C0007787 Transient ischemic attack HSDN C2024878 Cardiovascular surgery result: dyspnea C0034494 Rabies (disorder) HSDN C0240715 Perineal lump C1290288 Neoplasm of soft tissue of perineum UMLS C0424755 Fever symptoms C0997768 Glaucoma HSDN C0085636 Light sensitivity C1866504 Photosensitive trichothiodystrophy MalaCards|UMLS C4085211 Pain distress question C0041316 Lymph node tuberculosis HSDN C2875331 Spastic hemiplegia affecting left dominant side C0154694 Spastic hemiplegia UMLS C0426579 Anorexia symptom C0020517 Hypersensitivity HSDN C3641755 Have constipation C1443900 Inhalational botulism OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0001815 Primary myelofibrosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0026848 Myopathy HSDN C4084802 Usual severity diarrhea C0162534 Prion diseases HSDN C4085210 Usual severity pain C0751774 Nocturnal myoclonus syndrome HSDN C4049644 Depression C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C1963170 Hypothermia adverse event C0008325 Cholecystitis HSDN C0518090 Frequency of pain question C0018021 Goiter HSDN C0033790 Pseudobulbar palsy C0751072 Frontotemporal lobar degeneration HSDN C2024878 Cardiovascular surgery result: dyspnea C1963119 Stomach ulcer adverse event HSDN C3898969 Have been vomiting C0019061 Hemolytic-uremic syndrome HSDN C1557397 Adverse event associated with pain C0302497 Retrobulbar haemorrhage HSDN C0009763 Conjunctiva inflammation C1337030 Xpa gene HPO C0015672 Decreased energy C2707011 Behavioral symptoms:-:point in time:^patient:- HSDN C0043094 Weight gain C0162526 Aids-related opportunistic infections HSDN C2911645 Weight loss adverse event C0008497 Choriocarcinoma HSDN C0035232 Diaphragmatic paralysis C0679360 Foodborne disease HSDN C1962972 Proteinuria adverse event C2931253 Alport syndrome, dominant type MalaCards C3539892 Pelvic pain in front C0018965 Hematuria HSDN C1557397 Adverse event associated with pain C0014356 Enterocolitis HSDN C1279888 Proteinuria of undiagnosed cause C0007121 Bronchogenic carcinoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042749 Viremia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042487 Venous thrombosis HSDN C0497406 Over weight C0004352 Autistic disorder HSDN C0036659 Sensation disorder C0001973 Alcoholic intoxication, chronic HSDN C0027066 Myoclonic jerking C0021400 Influenza HSDN C4084802 Usual severity diarrhea C3812171 Bradycardia by ecg finding HSDN C0917801 Sleep disorder insomnia C2939186 Disturbance in mood UMLS C0857305 Thrombocytopenia purpura C0024419 Waldenstrom macroglobulinemia HSDN C0018772 Deafness C0751651 Mitochondrial diseases HSDN C0232466 Feeding difficulty C3809650 Bainbridge-ropers syndrome MalaCards C0522224 Palsied C1962971 Myocarditis adverse event HSDN C0036396 Sciatica C4085311 Depression - recess HSDN C0018681 Headache, cephalalgia C0751795 Head injury penetrating HSDN C1962972 Proteinuria adverse event C0343208 Essential mixed cryoglobulinemia OrphaNet|MalaCards C0035232 Diaphragmatic paralysis C0027626 Neoplasm invasiveness HSDN C1510417 Apraxia of gait C0035372 Rett syndrome MalaCards|HSDN|HPO C1279888 Proteinuria of undiagnosed cause C0007222 Cardiovascular diseases HSDN C1145670 Failure respiratory C2749106 Emery dreifuss muscular dystrophy 6, x linked MalaCards|HPO C4085222 Nausea C1253937 Pericardial effusion HSDN C0030193 Sense of pain C0040948 Trichostrongyliasis HSDN C3146279 Coma C2240378 Cleft palate on exam HSDN C0018681 Headache, cephalalgia C0012739 Disseminated intravascular coagulation HSDN C0086565 Liver function abnormal C1876175 Ataxia-telangiectasia variant MalaCards C0018784 Deafness sensorineural C0021361 Female infertility HSDN C0008031 Pain chest C0009244 Behavioral cognitive therapy HSDN C3541349 Syncope C1963138 Hypertension adverse event HSDN C0043094 Weight gain C0020544 Renal hypertension HSDN C0040822 D tremors C1706377 Memory device component HSDN C0312416 Morning sickness C3813607 Infantile gastroesophageal reflux HSDN C4084726 Distress cough C0014544 Epilepsy HSDN C0151786 Weakness muscle C0391817 Drug-induced autoim haem anaem OrphaNet|MalaCards C0023530 Leukopenia C0023381 Letterer-siwe disease MalaCards C3539022 Pelvic pain decreasing in severity C0085096 Peripheral vascular diseases HSDN C2203646 Jaundice C0038579 Substance abuse, intravenous HSDN C0015672 Decreased energy C0085129 Bronchial hyperreactivity HSDN C0151786 Weakness muscle C0004936 Mental disorders HSDN C0497406 Over weight C0016510 Foot diseases HSDN C0015468 Face pain C0266061 Open bite HSDN C4084802 Usual severity diarrhea C0033953 Psychosexual disorders HSDN C0007859 Pain neck C0002871 Anemia HSDN C2237041 Shox gene with short stature C3150942 Spondylocostal dysostosis 4, autosomal recessive MalaCards|HPO C0232466 Feeding difficulty C3281055 Psychomotor retardation, epilepsy, and craniofacial dysmorphism MalaCards C0019209 Large liver C3275508 Multiple congenital anomalies-hypotonia-seizures syndrome 2 MalaCards C4084802 Usual severity diarrhea C0034069 Pulmonary fibrosis HSDN C4084776 Weight loss C0023281 Leishmaniasis OrphaNet|HSDN|MalaCards C4084776 Weight loss C0342337 Insulin resistance syndrome, type b OrphaNet|MalaCards C3815497 Cough C2930674 Babesioses, human MalaCards C0019521 Hiccoughs C1145670 Respiratory failure HSDN C0000737 Abdomen pain C0025268 Multiple endocrine neoplasia type 2a OrphaNet C2237041 Shox gene with short stature C4014538 Helsmoortel-van der aa syndrome MalaCards C0009421 Comatose C0007131 Non-small cell lung carcinoma HSDN C0152169 Colic renal C0008350 Cholelithiasis HSDN C1279888 Proteinuria of undiagnosed cause C0020428 Hyperaldosteronism HSDN C3887638 Failure to thrive in infant C1969039 Renal tubular acidosis, distal, with normal red cell morphology HPO C2984058 Have pain C0037278 Skin diseases, infectious HSDN C0242936 Center pain C0018924 Hemarthrosis HSDN C0040485 Wryneck C0349785 Psychogenic torticollis UMLS C4084784 Diarrhea C0086647 Mucopolysaccharidosis type iiia HPO C0041657 Consciousness loss C0001940 Alcohol amnestic disorder HSDN C0557874 Global developmental delay C3279875 Cortical malformations, occipital MalaCards C0020450 Hyperemesis gravidarum C0040128 Thyroid diseases HSDN C4084769 Vomiting frequency C0013295 Duodenal ulcer HSDN C4085548 Usual severity dizziness C0009240 Cognition HSDN C0043094 Weight gain C0029463 Osteosarcoma HSDN C0018834 Brash C1837371 Sudden infant death with dysgenesis of the testes syndrome OrphaNet|HPO|MalaCards C4084788 Have dizziness C0015927 Intrauterine fetal demise HSDN C0042798 Vision dim C1866293 Retinal cone dystrophy 2 MalaCards C0028738 Nystagmus C1835916 Aicardi-goutieres syndrome 3 MalaCards|HPO C4084727 Cough frequency C0241158 Cicatrix skin HSDN C0857305 Thrombocytopenia purpura C0086543 Cataract nos HSDN C4084802 Usual severity diarrhea C0032066 Plague vaccines HSDN C0002962 Angina C0206062 Lung diseases, interstitial HSDN C1963252 Tremor adverse event C0041374 Tumor virus infections HSDN C0011991 Loose stools C0035078 Kidney failure HSDN C4085210 Usual severity pain C0025312 Meningomyelocele HSDN C1384666 Decreased hearing C0220666 Arthrogryposis multiplex congenita, distal, type iia MalaCards|HPO C0034933 Abnormal reflexes C0006112 Brain diseases, metabolic HSDN C0521788 Crackling ear sounds C0494559 Diseases of inner ear UMLS C4084723 Constipation C0151516 Thyroid hypoplasia OrphaNet|HPO C0375553 Continuous leakage of urine C0021167 Incontinence UMLS C0004604 Pain back C0014175 Endometriosis HSDN C1384666 Decreased hearing C0027643 Neoplasm recurrence, local HSDN C0020673 Hypothermia (central) (local) C0011849 Diabetes mellitus HSDN C0037771 Paraparesis spastic C0037231 Sjogren-larsson syndrome HSDN C0042963 Symptoms vomiting C0036216 Sarcoma, experimental HSDN C0026838 Spasticity muscle C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C3665347 Vision impaired C0267372 Intestinal lymphatic obstruction MalaCards C0009676 Confusion state C0004377 Automatism HSDN C0577561 Mass of ear structure C0013449 Ear neoplasms UMLS C0018681 Headache, cephalalgia C1547046 Kind of quantity - taste HSDN C0030486 Extremity paralysis, lower C0023220 Leg injury HSDN C1963184 Nystagmus adverse event C0011195 Dejerine-sottas disease (disorder) HPO C0010200 Cough symptom C0030567 Parkinson disease HSDN C2219925 Feeling persecuted, vigilant against perceived treachery C0747249 Paranoid ideation UMLS C0042025 Urinary incontinence stress C0013922 Embolism HSDN C2911645 Weight loss adverse event C1836706 Hyperthyroidism, nonautoimmune MalaCards C0018772 Deafness C0016053 Fibromyalgia HSDN C4085549 Dizziness C2586211 Thrombosis of blood vessel HSDN C0019079 Bloody sputum C0003509 Aortitis, nos HSDN C4084766 Vomiting C0302148 Blood clot HSDN C2984057 Have nausea C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4084776 Weight loss C0040336 Tobacco use disorder HSDN C0857051 Bad dream C0236816 Stress disorders, traumatic, acute MalaCards C0042025 Urinary incontinence stress C0011168 Deglutition disorders HSDN C0043094 Weight gain C0014547 Epilepsies, partial HSDN C0018991 Paralysis one side of body C2711849 Hemiplegia as late effect of cerebrovascular disease UMLS C3829611 Nausea frequency C0162565 Acute intermittent porphyria MalaCards|HPO C1384666 Decreased hearing C0008525 Choroideremia HSDN C1549543 Administration method - pain C0162820 Dermatitis, allergic contact HSDN C3898969 Have been vomiting C0002895 Anemia, sickle cell HSDN C1557397 Adverse event associated with pain C0042024 Urinary incontinence HSDN C0030554 Abnormal sensation C0010068 Coronary heart disease HSDN C0009676 Confusion state C0151744 Myocardial ischemia HSDN C0039231 Heartbeats increased C1857338 Deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy MalaCards C4084767 Bothered by vomiting C0242966 Systemic inflammatory response syndrome HSDN C0518090 Frequency of pain question C0042568 Vertebrobasilar insufficiency HSDN C0151786 Weakness muscle C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0025202 Melanoma HSDN C0032617 High urine output C0030297 Pancreatic neoplasm HSDN C0020672 Body temperature decreased C0040185 Tibia fracture HSDN C0494475 Seizure generalized tonic clonic C1853215 Autosomal recessive frontotemporal pachygyria OrphaNet|MalaCards C3146279 Coma C0020461 Hyperkalemia HSDN C1963184 Nystagmus adverse event C0751038 Cockayne syndrome, type ii HPO C2984058 Have pain C0020120 Engineering humans HSDN C1963091 Diarrhea adverse event C0022423 Judgement HSDN C2984058 Have pain C0020981 Angioimmunoblastic lymphadenopathy HSDN C0024312 Lymphocytopenia C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C1962972 Proteinuria adverse event C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0009792 Consciousness disorder C0027873 Neuromyelitis optica HSDN C0036396 Sciatica C0018799 Heart diseases HSDN C0007758 Cerebellar ataxia C0271829 Pendred's syndrome MalaCards|HPO C0857305 Thrombocytopenia purpura C0017168 Gastroesophageal reflux disease HSDN C0030193 Sense of pain C0014122 Subacute bacterial endocarditis HSDN C1963091 Diarrhea adverse event C0242422 Parkinsonian disorders HSDN C0851578 Disorder sleep C0011875 Diabetic angiopathies HSDN C0020672 Body temperature decreased C0010054 Coronary arteriosclerosis HSDN C0751295 Memory loss or impairment C0038454 Cerebrovascular accident UMLS C0237326 Defecation pain C1866927 Smcr HPO C0040460 Dental pain C1548578 Location characteristic id - smoking HSDN C0015469 Facial paralysis C0015393 Eye abnormalities HSDN C1000483 Genus anemia C0016037 Fibrodysplasia ossificans progressiva MalaCards|HPO C0015672 Decreased energy C0037939 Spinal neoplasms HSDN C0019209 Large liver C0221757 Alpha 1-antitrypsin deficiency OrphaNet|HPO C0030200 Intractable pain C0022661 Kidney failure, chronic HSDN C0036659 Sensation disorder C0023529 Leukomalacia, periventricular HSDN C0518090 Frequency of pain question C0002448 Ameloblastoma HSDN C0030975 Disorders perception C0006434 Burn injury HSDN C3541349 Syncope C0011609 Drug eruptions HSDN C0600142 Flash hot C0853762 Aggravation of hot flushes UMLS C2984058 Have pain C0037999 Splenic neoplasms HSDN C2237041 Shox gene with short stature C3279843 Mosaic variegated aneuploidy syndrome 2 MalaCards C0013404 Respiratory difficulty C0517555 Venous thrombosis after immobility HSDN C1963281 Vomiting adverse event C0020649 Hypotension HSDN C0032617 High urine output C1846980 Senior-loken syndrome 3 MalaCards|UMLS C0424755 Fever symptoms C0018203 Chronic granulomatous disease OrphaNet|HSDN|HPO|MalaCards C4085210 Usual severity pain C0001957 Alcohol withdrawal delirium HSDN C0011168 Disorder deglutition C1858351 Spinocerebellar ataxia 11 OrphaNet|HPO|MalaCards C0012833 Dizzy C0031117 Peripheral neuropathy HSDN C0018524 Hallucinate C0038874 Supratentorial neoplasms HSDN C4084802 Usual severity diarrhea C1857231 Lactase persistence HPO C0040034 Thrombocytopenia C0024131 Lupus vulgaris MalaCards C0518090 Frequency of pain question C0038354 Stomach diseases HSDN C3463815 Feel fatigue C0235387 Porphyria type syndrome OrphaNet C0341866 Menopausal sleeplessness C0080276 Disorder of the genitourinary system UMLS C0042963 Symptoms vomiting C0702166 Acne HSDN C2024893 Cardiovascular surgery result: fatigue C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal OrphaNet|HPO C0034155 Thrombotic thrombocytopenic purpura C4084909 Depression subordinate domain HSDN C0036572 Convulsion C0220722 Cerebrooculofacioskeletal syndrome 1 OrphaNet|HPO C1963249 Tinnitus adverse event C0002871 Anemia HSDN C0002962 Angina C0276275 Disease due to parvoviridae HSDN C0233794 Memory impaired C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0349588 Stature short C1959626 Mevalonic aciduria OrphaNet|HPO|MalaCards C4084788 Have dizziness C0002940 Aneurysm HSDN C0022408 Disorder joint C2745959 Spondyloepiphyseal dysplasia, congenita MalaCards C0020903 Illusion C1690964 Cataract HSDN C0030193 Sense of pain C1963148 Iron overload adverse event HSDN C0026838 Spasticity muscle C0162672 Merrf syndrome MalaCards|HPO C0010200 Cough symptom C1711276 Carcinosarcoma of lung UMLS C0015672 Decreased energy C1963119 Stomach ulcer adverse event HSDN C2919142 Short stature adverse event C1845285 Martin-probst deafness-mental retardation syndrome OrphaNet|MalaCards C2017374 Right leg soft tissue swelling with bluish discoloration C0151907 Discoloration of skin UMLS C0086565 Liver function abnormal C4014605 Polyglucosan body myopathy 1 with or without immunodeficiency MalaCards C0037763 Spasm C0004935 Animal ethology HSDN C1384666 Decreased hearing C2673873 Bardet-biedl syndrome 13 HPO C0232461 Increased appetite C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C0020455 Hypergammaglobulinemia C0003850 Arteriosclerosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016052 Fibromuscular dysplasia HSDN C0018784 Deafness sensorineural C0349231 Phobic anxiety disorder HSDN C1557397 Adverse event associated with pain C2267227 Bulimia nervosa HSDN C0030193 Sense of pain C0009663 Condylomata acuminata HSDN C0151786 Weakness muscle C0268647 Lysinuric protein intolerance MalaCards|HPO|UMLS C4084769 Vomiting frequency C0042880 Vitamin k deficiency HSDN C0349588 Stature short C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0456889 Enteropathy-associated t-cell lymphoma HSDN C0030552 Paralysis partial C3151753 Combined oxidative phosphorylation deficiency 6 MalaCards C4085210 Usual severity pain C0004775 Bartter disease HSDN C0850758 Pain pelvic C0520720 Cyst nerve root HSDN C4084725 Usual severity cough C2073625 X-ray of chest: pleural effusion HSDN C0018991 Paralysis one side of body C0004442 Avoidance learning HSDN C0034155 Thrombotic thrombocytopenic purpura C0036830 Serum sickness HSDN C4085211 Pain distress question C0010481 Cushing syndrome HSDN C0221423 Ailment C0558116 Altered body image UMLS C0030975 Disorders perception C0001163 Vestibulocochlear nerve diseases HSDN C3898969 Have been vomiting C3661523 Congenital intestinal aganglionosis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0020545 Hypertension, renovascular HSDN C0700078 Deep tendon reflex decrease C0393814 Hereditary liability to pressure palsies HPO C0426579 Anorexia symptom C2937358 Cerebral hemorrhage HSDN C0000737 Abdomen pain C0238337 Pancreas, cystadenocarcinoma UMLS C4084802 Usual severity diarrhea C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C3887638 Failure to thrive in infant C0038238 Steatorrhea HSDN C0018784 Deafness sensorineural C2717757 Retinocochleocerebral vasculopathies OrphaNet|MalaCards C0036572 Convulsion C1836287 Cerebrorenodigital syndrome with limb malformations and triradiate acetabula OrphaNet|MalaCards C0018681 Headache, cephalalgia C0346328 Meningiomas nerve optic sheath UMLS C0036572 Convulsion C0027686 Pathologic neovascularization HSDN C3641755 Have constipation C0038436 Post-traumatic stress disorder HSDN C1963091 Diarrhea adverse event C0032897 Prader-willi syndrome HSDN C0015970 Fever unknown origin C2697932 Loeys-dietz syndrome HSDN C0026826 High muscle tone C0600041 Infective cystitis HSDN C0234979 Dysdiadochokinesia C3553816 Spinocerebellar ataxia, autosomal recessive 13 MalaCards|UMLS C0518090 Frequency of pain question C0162820 Dermatitis, allergic contact HSDN C0019572 Hairiness C3550903 Cornelia de lange syndrome 5 MalaCards C0151825 Ostalgia C0265514 Dermatofibrosis lenticularis disseminata OrphaNet|HPO|MalaCards C0020672 Body temperature decreased C0026848 Myopathy HSDN C0086437 Joint hypermobility C0024796 Marfan syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0238461 Anaplastic thyroid carcinoma OrphaNet C1963281 Vomiting adverse event C0038536 Subcutaneous emphysema HSDN C0030193 Sense of pain C0079772 T-cell lymphoma HSDN C1962972 Proteinuria adverse event C0020623 Hypolipoproteinemias HSDN C0011991 Loose stools C0039446 Telangiectasis HSDN C3815497 Cough C0025063 Mediastinal neoplasms HSDN C2237041 Shox gene with short stature C0086431 Hurler-scheie syndrome OrphaNet|HPO C1961131 Cough adverse event C0001584 Adolescent psychology HSDN C0522224 Palsied C0033586 Failure, prosthesis HSDN C4085210 Usual severity pain C0022573 Keratoconjunctivitis HSDN C0039070 Collapse fleeting C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0162298 Stiffness joints C1849928 Phaver syndrome MalaCards C0005745 Blepharoptosis C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards C0023015 Language handicap C0022698 Kinesics HSDN C4084774 Have weight loss C0013274 Patent ductus arteriosus HSDN C0012833 Dizzy C0393911 Pure autonomic failure HSDN C4084725 Usual severity cough C0549472 Pneumonia, cholesterol MalaCards C4085642 Level of joint stiffness C2678439 Cranioosteoarthropathy OrphaNet|HPO C0086565 Liver function abnormal C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO C4084766 Vomiting C0043208 Wolman disease HPO C0033774 Skin pruritus C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0234357 Adiadokokinesis C0007760 Cerebellar diseases UMLS C1557397 Adverse event associated with pain C0015302 External exotoses HSDN C0042571 Vertigo subjective C0004303 Auditory disease, central HSDN C0002962 Angina C0036202 Sarcoidosis HSDN C0038002 Spleen enlargement C0023241 Legionnaires' disease MalaCards C0003811 Cardiac rhythm disturbance C3854315 Pseudoprimary hyperaldosteronism MalaCards C2911647 Weight gain adverse event C0027121 Myositis HSDN C2911647 Weight gain adverse event C0005695 Bladder neoplasm HSDN C0040822 D tremors C1843891 Spinocerebellar ataxia 21 UMLS C0398650 Idiopathic thrombocytopenia purpura C0012236 Digeorge syndrome HSDN C0025287 Meningitis-like C0007274 Carotid artery thrombosis HSDN C0025287 Meningitis-like C0037942 Spinal osteophytosis HSDN C0242936 Center pain C0020626 Hypoparathyroidism HSDN C4049602 Hyperactivity C1527231 Adrenomyeloneuropathy MalaCards C0004134 Dyssynergia C0020517 Hypersensitivity HSDN C3641755 Have constipation C1963215 Pneumothorax adverse event HSDN C2919142 Short stature adverse event C2931737 Hersh podruch weisskopk syndrome MalaCards C0030193 Sense of pain C0037413 Social dominance HSDN C0000737 Abdomen pain C3899979 Bclc stage b hepatocellular carcinoma UMLS C1145670 Failure respiratory C1858118 Muscular dystrophy, congenital, 1b MalaCards C3494358 Characteristic, prodromal C0026769 Multiple sclerosis HSDN C0221752 Rbc urine C0220987 Hereditary orotic aciduria MalaCards C0151889 Reflexes tendon increased C1968804 Plasminogen deficiency, type i MalaCards C0027497 Queasy C0018809 Heart neoplasm HSDN C4084725 Usual severity cough C0008350 Cholelithiasis HSDN C4084776 Weight loss C0559260 Congenital scoliosis HSDN C4085211 Pain distress question C0003615 Appendicitis MalaCards C4084802 Usual severity diarrhea C0021345 Infectious mononucleosis HSDN C0151786 Weakness muscle C0272258 Cryoglobulinemia, primary MalaCards C2024878 Cardiovascular surgery result: dyspnea C0008626 Congenital chromosomal disease HSDN C3898969 Have been vomiting C0162872 Aortic aneurysm, thoracic HSDN C0019079 Bloody sputum C1302808 Myopericytoma HSDN C0270790 Quadriparesis C0038454 Cerebrovascular accident UMLS C0042755 Virilisation C0023890 Liver cirrhosis HSDN C4084784 Diarrhea C0042164 Uveitis HSDN C1963167 Memory impairment adverse event C0398746 Gluthathione synthetase deficiency MalaCards C0151786 Weakness muscle C0085920 Brachial neuralgia MalaCards C0010200 Cough symptom C1334683 Endodermal sinus neoplasm of mediastinum UMLS C0004134 Dyssynergia C0020550 Hyperthyroidism HSDN C0011206 Delirium acute C1963138 Hypertension adverse event HSDN C1279888 Proteinuria of undiagnosed cause C1852759 Papillorenal syndrome MalaCards|HPO C0542476 Forgetful C0027831 Neurofibromatosis 1 OrphaNet C0010200 Cough symptom C0031149 Peritoneal neoplasms HSDN C1000483 Genus anemia C0238386 Cronkhite-canada disease MalaCards C0010200 Cough symptom C0037051 Behavior illness HSDN C1971624 Appetite absent C0031090 Periodontal diseases HSDN C0027498 Nausea vomiting C0079770 Lymphoma, small noncleaved-cell MalaCards|HPO C0035229 Respiratory function impaired C1843504 Pontocerebellar hypoplasia type 1 HPO C2919142 Short stature adverse event C0220666 Arthrogryposis multiplex congenita, distal, type iia MalaCards|HPO C0026838 Spasticity muscle C0409959 Osteoarthritis, knee HSDN C0030552 Paralysis partial C0019163 Hepatitis b HSDN C0557874 Global developmental delay C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C0019209 Large liver C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C0027497 Queasy C1962958 Hematoma adverse event HSDN C0030193 Sense of pain C1332974 Childhood conventional osteosarcoma UMLS C0030193 Sense of pain C0040411 Tongue neoplasms HSDN C0520909 Ponv C4050613 Anxiety scale (basc-2) HSDN C0020672 Body temperature decreased C0236969 Substance-related disorders HSDN C4085211 Pain distress question C0040820 Trematode infections HSDN C1963281 Vomiting adverse event C0037315 Sleep apnea syndromes HSDN C0043094 Weight gain C0030790 Pelvis infection HSDN C0344232 Blurred vision C0035317 Retinal hemorrhage MalaCards C0043352 Absent salivary secretion C0859976 Idiopathic achalasia of esophagus MalaCards C0518090 Frequency of pain question C1739395 Takotsubo cardiomyopathy HSDN C0026838 Spasticity muscle C4225393 3-methylglutaconic aciduria with cataracts, neurologic involvement, and neutropenia UMLS C0013421 Dystonia C4024961 Metachromatic leukodystrophy variant MalaCards C2919142 Short stature adverse event C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C0029163 Hemorrhage mouth C0008925 Cleft palate HSDN C0009676 Confusion state C0018799 Heart diseases HSDN C0036572 Convulsion C0009782 Connective tissue diseases HSDN C0150055 Pain chronic C0021364 Male infertility HSDN C4084776 Weight loss C3244301 Coverage level - family HSDN C0027066 Myoclonic jerking C0042373 Vascular diseases HSDN C3463815 Feel fatigue C0042487 Venous thrombosis HSDN C0010520 Skin cyanosis C0039446 Telangiectasis HSDN C4084784 Diarrhea C0029445 Bone necrosis HSDN C0751295 Memory loss or impairment C0010324 Crigler najjar syndrome, type 1 MalaCards|HPO C0018784 Deafness sensorineural C0027888 Hereditary motor and sensory neuropathies HSDN C2315100 Pediatric failure to thrive C3887949 Apparent mineralocorticoid excess MalaCards C0043094 Weight gain C0205788 Histiocytoid hemangioma HSDN C0018772 Deafness C1856476 Gaucher disease, type iiic OrphaNet|HPO C0423708 Obturator neuralgia C0574718 Lower limb nerve lesion UMLS C0033774 Skin pruritus C1860167 Ackerman syndrome MalaCards C0024032 Birth weight subnormal C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C0033377 Caudal displacement C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C0040034 Thrombocytopenia C0175703 Thrombocytopenia-absent radius syndrome OrphaNet|HPO|MalaCards C0013604 Edematous C0152054 Therapeutic touch HSDN C4084773 Bothered by weight gain C0242550 Behavior, risk reduction HSDN C4084776 Weight loss C0027059 Myocarditis HSDN C2237041 Shox gene with short stature C1860823 Trichorhinophalangeal syndrome, type iii MalaCards|HPO C1963091 Diarrhea adverse event C0020619 Hypogonadism HSDN C0018524 Hallucinate C0268568 Classic maple syrup urine disease HPO C2077990 Intolerance to milk products used as a filler in pills C0022951 Lactose intolerance UMLS C2984058 Have pain C0013274 Patent ductus arteriosus HSDN C4084766 Vomiting C0001623 Adrenal gland hypofunction HSDN C0030552 Paralysis partial C0035309 Retinal diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0032343 Poisoning HSDN C0028738 Nystagmus C0265249 Mietens' syndrome MalaCards C2242996 Tingling C1145628 Autonomic nervous system disorders HSDN C2024878 Cardiovascular surgery result: dyspnea C0023467 Leukemia, myelocytic, acute HSDN C0034124 Pupillary disorder C0042338 Herpesvirus 3, human HSDN C0040822 D tremors C3281200 Leukoencephalopathy, brain calcifications, and cysts UMLS C4085317 Diarrhea frequency C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C1963167 Memory impairment adverse event C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C0033774 Skin pruritus C2711591 Infection by anisakidae HSDN C0684343 Pseudophakia C1417917 Oat gene HSDN C3494358 Characteristic, prodromal C0001580 Adolescent behavior HSDN C0009421 Comatose C1855116 Methylmalonic aciduria, mut(-) type HPO C4084769 Vomiting frequency C0025472 Mesenteric vascular occlusion HSDN C0009421 Comatose C0003811 Cardiac arrhythmia HSDN C0004604 Pain back C1962983 Cataract adverse event HSDN C0027497 Queasy C0011875 Diabetic angiopathies HSDN C0030552 Paralysis partial C2711227 Steatohepatitis HSDN C4085222 Nausea C0086543 Cataract nos HSDN C0033377 Caudal displacement C0079661 Klein's syndrome MalaCards C3829611 Nausea frequency C0275148 Poisoning of animal by plant HSDN C0151740 Intracranial hypertension C0027859 Acoustic neuroma HPO C1557397 Adverse event associated with pain C0007350 Cat disease HSDN C1963077 Bone pain adverse event C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0241210 Speaking delay C2675463 Chromosome 15q26-qter deletion syndrome MalaCards C0041657 Consciousness loss C0033845 Pseudotumor cerebri HSDN C0015672 Decreased energy C0020522 Delayed hypersensitivity HSDN C0234471 Conduction aphasia C0021228 Variability of individual responses HSDN C4084766 Vomiting C0524910 Hepatitis c, chronic MalaCards C1549543 Administration method - pain C0043407 Yersinia infections HSDN C0009806 Constipate C0026650 Movement disorders HSDN C1263846 Attention deficit disorder with hyperactivity C0432246 Microcephalic osteodysplastic primordial dwarfism, type ii HPO C4085211 Pain distress question C0002438 Amebiasis HSDN C2242996 Tingling C0036974 Shock HSDN C0727671 Red cross toothache drops C1962986 Glaucoma adverse event HSDN C1963170 Hypothermia adverse event C0037930 Spinal cord neoplasms HSDN C0557874 Global developmental delay C2678223 Mental retardation, x-linked, with panhypopituitarism HPO C0030193 Sense of pain C0014065 Congenital cerebral hernia HSDN C1963274 Vasculitis adverse event C0009447 Common variable immunodeficiency MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0520799 Acute radiation syndrome HSDN C0424755 Fever symptoms C0031039 Effusion pericardial HSDN C0022346 Yellow skin C0018916 Hemangioma HSDN C1959630 Eye pain adverse event C0032816 Post-concussion headache HSDN C0009806 Constipate C0017636 Glioblastoma HSDN C0027497 Queasy C0006309 Brucellosis HSDN C3815497 Cough C0152018 Esophageal carcinoma OrphaNet|MalaCards C0575081 Abnormal gait C0025237 Melnick-needles syndrome MalaCards|HPO C0036572 Convulsion C0752143 Intracranial thrombosis HSDN C4084775 Usual severity weight loss C1854336 Paragangliomas 3 MalaCards C0007758 Cerebellar ataxia C0023524 Leukoencephalopathy, progressive multifocal HSDN C4084802 Usual severity diarrhea C0016663 Pathological fracture HSDN C1549543 Administration method - pain C0236664 Alcohol-related disorders HSDN C0349588 Stature short C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0018784 Deafness sensorineural C0795902 Coloboma, cleft lip-palate and mental retardation syndrome OrphaNet|HPO|MalaCards C4085658 Usual severity lack of appetite C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0008031 Pain chest C0008350 Cholelithiasis HSDN|UMLS C2029884 Hearing loss by exam C0221357 Brachydactyly HSDN C0004134 Dyssynergia C1412760 Bckdhb gene HSDN C0009398 Color vision defects C0012979 Canine disease HSDN C4084784 Diarrhea C3810147 Immunodeficiency 19 MalaCards C0018784 Deafness sensorineural C1846839 Deafness, autosomal recessive 31 MalaCards|HPO C0036572 Convulsion C0393590 Fahr's syndrome (disorder) OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0042075 Urologic diseases HSDN C0020672 Body temperature decreased C0011265 Presenile dementia HSDN C1963065 Apnea adverse event C0008625 Chromosome aberrations HSDN C3815497 Cough C1963067 Atrial fibrillation adverse event HSDN C3641756 Have diarrhea C1959620 Dihydropyrimidine dehydrogenase deficiency HSDN C4049644 Depression C0268425 Alstrom syndrome MalaCards|HPO C4084767 Bothered by vomiting C0948089 Acute coronary syndrome HSDN C0557874 Global developmental delay C2931011 Congenital disorder of glycosylation, type 2g MalaCards C0042798 Vision dim C1762616 Meningioma, benign, no icd-o subtype HSDN C0241137 Skin pallor C1963139 Hypopigmentation adverse event HSDN C0013604 Edematous C0008628 Chromosome deletion HSDN C0025287 Meningitis-like C0021368 Inflammation UMLS C0042940 Disorder of voice C0008625 Chromosome aberrations HSDN C0150055 Pain chronic C3494322 Narrative therapy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026590 Child mother relationship HSDN C1962972 Proteinuria adverse event C0015624 Fanconi syndrome HPO C1319542 On examination - left eye proliferative diabetic retinopathy C0011849 Diabetes mellitus UMLS C0030232 Color loss C2936826 Fumaric aciduria MalaCards|HPO C0751837 Gait ataxic C0030569 Secondary parkinson disease HSDN C0085636 Light sensitivity C1859844 Leber congenital amaurosis, type ii (disorder) MalaCards|HPO C0015402 Hemorrhage eye C0019087 Hemorrhagic disorders HSDN C0030552 Paralysis partial C1963215 Pneumothorax adverse event HSDN C1557397 Adverse event associated with pain C0008698 Maxillary sinusitis chronic HSDN C2242996 Tingling C0007137 Squamous cell carcinoma HSDN C0013395 Indigestion C0051981 Anti-leprosy vaccine HSDN C1384666 Decreased hearing C0039128 Syphilis HSDN C0000737 Abdomen pain C2981378 Stage iia small intestinal cancer UMLS C0042963 Symptoms vomiting C3874311 Vomiting of fecal matter UMLS C4085317 Diarrhea frequency C0025162 Megacolon toxic HSDN C0042571 Vertigo subjective C1547940 Specimen source codes - ulcer HSDN C0019572 Hairiness C1859566 Bardet-biedl syndrome 8 HPO C0497406 Over weight C0027743 Nerve compression syndrome HSDN C0004604 Pain back C0577663 Back pain psychogenic UMLS C4085210 Usual severity pain C0037417 Identification, social HSDN C0020673 Hypothermia (central) (local) C0795623 Hepatitis a vaccine, inactivated HSDN C0011991 Loose stools C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0401158 Vomiting after git surgery C0032787 Postoperative complications UMLS C0018681 Headache, cephalalgia C0038395 Streptococcal infections HSDN C1962972 Proteinuria adverse event C0030354 Papilloma HSDN C0020796 Profoundly mentally retarded C2936826 Fumaric aciduria MalaCards|HPO C3463815 Feel fatigue C0034362 Q fever HSDN C1384666 Decreased hearing C0018051 Gonadal dysgenesis HSDN C0037317 Sleep disturbance C0027404 Narcolepsy OrphaNet|UMLS|MalaCards C2010810 Generalized lesions including the palms C0037284 Skin lesion UMLS C1963065 Apnea adverse event C1720922 Respiratory aspiration HSDN C0018772 Deafness C3164344 Adult onset autosomal dominant leukodystrophy HPO C1963093 Dizziness adverse event C0025286 Meningioma HSDN C0018681 Headache, cephalalgia C2930674 Babesioses, human MalaCards C4084768 Usual severity vomiting C0007787 Transient ischemic attack HSDN C4084768 Usual severity vomiting C0302148 Blood clot HSDN C4085548 Usual severity dizziness C0006430 Burning mouth syndrome HSDN C0812426 Kidney problem C0543795 Renal tubular acidosis hyperchloremic UMLS C0242936 Center pain C0162532 Variegate porphyria MalaCards C0009421 Comatose C0035613 Rift valley fever MalaCards C4085222 Nausea C0003467 Anxiety HSDN C0013362 Dysarthrias C1858583 Hemosiderosis, systemic, due to aceruloplasminemia HPO C2203646 Jaundice C0162531 Hereditary coproporphyria HPO C1384666 Decreased hearing C0035372 Rett syndrome MalaCards C0027796 Neuralgias C0152179 Disease vagus nerve HSDN C0013604 Edematous C0037305 Neoplasm, skull HSDN C0518090 Frequency of pain question C0340629 Aortic aneurysm without mention of rupture nos HSDN C0013604 Edematous C0553580 Ewings sarcoma HSDN C0027066 Myoclonic jerking C0003850 Arteriosclerosis HSDN C0042963 Symptoms vomiting C0020303 Hydropneumothorax HSDN C0151786 Weakness muscle C0042131 Uterine diseases HSDN C0085636 Light sensitivity C0268497 Brown oculocutaneous albinism MalaCards C3815497 Cough C0020542 Pulmonary hypertension HSDN C2911647 Weight gain adverse event C0015579 Family characteristics HSDN C4084766 Vomiting C0029458 Osteoporosis, postmenopausal HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0005779 Blood coagulation disorders HSDN C0019209 Large liver C1801959 Histiocytic medullary reticulosis (disorder) MalaCards|HPO C0042024 Urine incontinence C0021845 Intestinal perforation HSDN C0030193 Sense of pain C0030312 Pancytopenia HSDN C1971624 Appetite absent C0011854 Diabetes mellitus, insulin-dependent HSDN C1963087 Constipation adverse event C1548484 Rheumatic fever vaccine HSDN C0349588 Stature short C2675336 Duplication 15q11-q13 syndrome MalaCards|HPO C0035229 Respiratory function impaired C0268412 Infantile hypophosphatasia MalaCards C2203646 Jaundice C0022661 Kidney failure, chronic HSDN C2919142 Short stature adverse event C0432365 Thalidomide embryopathy syndrome OrphaNet|MalaCards C1963249 Tinnitus adverse event C0006663 Calcinosis HSDN C3541349 Syncope C0078888 Accelerated idioventricular rhythm HSDN C4084784 Diarrhea C1261473 Sarcoma HSDN C4085222 Nausea C0036421 Systemic scleroderma HSDN C0033377 Caudal displacement C3273031 Hnec MalaCards C1963093 Dizziness adverse event C0314657 Genetic predisposition HSDN C0042940 Disorder of voice C0008626 Congenital chromosomal disease HSDN C1279888 Proteinuria of undiagnosed cause C0033975 Psychotic disorders HSDN C0023380 Lethargy C0004048 Breathing HSDN C0011991 Loose stools C0025299 Meningocele HSDN C0026603 Motion sickness C0236969 Substance-related disorders HSDN C0344315 Mood depressed C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0349788 Arrhythmogenic right ventricular dysplasia HSDN C1971624 Appetite absent C2706915 Language:-:point in time:^patient:- HSDN C0012569 Double vision C0036341 Schizophrenia HSDN C0085636 Light sensitivity C1848413 Trichothiodystrophy, type 1 MalaCards|HPO C0150055 Pain chronic C1556682 Adverse event associated with infection HSDN C0040822 D tremors C0040156 Thyrotoxicosis HSDN C0518090 Frequency of pain question C0023485 Precursor b-cell lymphoblastic leukemia-lymphoma HSDN C0030486 Extremity paralysis, lower C0029405 Osteitis fibrosa cystica HSDN C4084773 Bothered by weight gain C0011265 Presenile dementia HSDN C0019521 Hiccoughs C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C0234146 Absent reflex C1956125 Alagille syndrome 1 HPO C2032396 Pelvic pain on the right C0206767 Neoplasms, cystic, mucinous, and serous HSDN C0041105 Jaw spasm C0553730 Calcium pyrophosphate deposition disease HSDN C0151825 Ostalgia C3900106 Adult b acute lymphoblastic leukemia with t(9;22)(q34;q11.2); bcr-abl1 UMLS C1549543 Administration method - pain C0393735 Headache disorders HSDN C0039870 Leanness C0007137 Squamous cell carcinoma HSDN C0013604 Edematous C0033785 Pseudarthrosis HSDN C1963252 Tremor adverse event C0037929 Spinal cord injuries HSDN C3274924 Have been coughing C0034531 Experimental radiation injuries HSDN C2315100 Pediatric failure to thrive C1857555 Hsd11b2, arg337cys HPO C1963249 Tinnitus adverse event C1260386 Glucocorticoid-remediable aldosteronism HPO C4085548 Usual severity dizziness C0013502 Echinococcosis HSDN C0033774 Skin pruritus C0439840 Reflex motion descriptor HSDN C0036572 Convulsion C1855126 3-methylglutaconic aciduria type iv OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0268307 Conjugated hyperbilirubinemia MalaCards C0002962 Angina C0027868 Neuromuscular diseases HSDN C0398650 Idiopathic thrombocytopenia purpura C0749095 Subdural hematoma chronic HSDN C0270948 Neurogenic muscular atrophy C0162671 Melas syndrome MalaCards|HPO C4084775 Usual severity weight loss C0009651 Conditioning operant HSDN C0040264 Ear ringing sound C0038531 Subclavian artery stenosis HSDN C4084802 Usual severity diarrhea C0005941 Bone diseases, developmental HSDN C0012833 Dizzy C0027666 Neoplasms, radiation-induced HSDN C4084768 Usual severity vomiting C0344479 Spinal cord myelodysplasia HSDN C0232493 Epigastric pain C0744304 Gastric ulcer pyloric channel perforation UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0023743 Linitis plastica HSDN C0022346 Yellow skin C0032851 Disease poultry HSDN C0028738 Nystagmus C1866282 Ceroid lipofuscinosis, neuronal, 6 MalaCards C0036396 Sciatica C4084909 Depression subordinate domain HSDN C0015230 Exanthem C0275525 Exanthematous infection, nos UMLS C3829611 Nausea frequency C1550639 Specimen type - fistula HSDN C3539895 Pelvic pain occurs with bowel movement C0236969 Substance-related disorders HSDN C0851578 Disorder sleep C0038454 Cerebrovascular accident HSDN C0002962 Angina C0015461 Facial neoplasms HSDN C4084775 Usual severity weight loss C0034531 Experimental radiation injuries HSDN C0019079 Bloody sputum C0917875 Esophageal diverticulosis HSDN C2237041 Shox gene with short stature C3281138 Chromosome 17q12 deletion syndrome MalaCards C0042025 Urinary incontinence stress C3163620 Hypotension adverse event HSDN C4049602 Hyperactivity C3150675 Chromosome 15q24 duplication syndrome HPO C1963170 Hypothermia adverse event C0003467 Anxiety HSDN C0011991 Loose stools C0041909 Gastrointestinal bleed upper UMLS C4084774 Have weight loss C0153414 Malignant neoplasm of middle third of esophagus MalaCards C0030975 Disorders perception C2586211 Thrombosis of blood vessel HSDN C0424755 Fever symptoms C0152937 Primary pneumonic plague DiseaseOntology|MalaCards C0028738 Nystagmus C1846496 Gaze palsy, familial horizontal, with progressive scoliosis OrphaNet|HPO C0011991 Loose stools C0746693 Mycobacterium avium complex disseminated UMLS C0042963 Symptoms vomiting C0000735 Abdominal neoplasms HSDN C0034933 Abnormal reflexes C0080178 Spina bifida HSDN C2984058 Have pain C0549567 Pigmentation disorders HSDN C3887638 Failure to thrive in infant C0023903 Liver neoplasms HSDN C0015672 Decreased energy C0740766 Acute pneumonia UMLS C0030193 Sense of pain C0018482 Haemophilus infections HSDN C1557397 Adverse event associated with pain C0012243 Digestive system neoplasms HSDN C0043352 Absent salivary secretion C0265363 Urethral obstruction sequence MalaCards C4084774 Have weight loss C0027625 Circulating neoplastic cells HSDN C0035078 Failure kidney C0043397 Yellow fever, jungle MalaCards C0151908 Dry skin C3887992 Thyrotropin-releasing hormone deficiency MalaCards C1963093 Dizziness adverse event C0027831 Neurofibromatosis 1 HSDN C0026603 Motion sickness C0004442 Avoidance learning HSDN C0042256 Vaginal pruritus C0042251 Vaginal diseases UMLS C4085211 Pain distress question C0024954 Maxillary neoplasms HSDN C2919142 Short stature adverse event C1421143 Trh gene HPO C0018681 Headache, cephalalgia C1959582 Pten hamartoma tumor syndrome MalaCards C0038990 Sweats C1833030 Palmoplantar keratoderma, nonepidermolytic MalaCards C4085222 Nausea C0032914 Pre-eclampsia HSDN C0040822 D tremors C3888317 Sialidosis, type 2 OrphaNet C3714552 Strength decreased C0032541 Polyneuritis UMLS C0036572 Convulsion C0008497 Choriocarcinoma HSDN C0036572 Convulsion C1546533 Specimen source codes - abscess HSDN C0234523 Apraxia, classic C3850024 Transcranial direct current stimulation HSDN C1384666 Decreased hearing C0796032 Malpuech facial clefting syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0085083 Ovarian hyperstimulation syndrome HSDN C3815497 Cough C0011853 Diabetes mellitus, experimental HSDN C0027498 Nausea vomiting C3714497 Reactive airway disease UMLS C0242936 Center pain C0007527 Cecal disease HSDN C0013390 Cramps menstrual C0010068 Coronary heart disease HSDN C1549543 Administration method - pain C3887650 Adult rickets HSDN C0022346 Yellow skin C1856403 Etfb deficiencies HPO C4042891 Sleep wake disorders C0042514 Tachycardia, ventricular HSDN C0004134 Dyssynergia C0238265 Encephalopathy, callosal demyelinating HSDN C0231528 Muscle pain generalized C0035597 Pox rickettsial DiseaseOntology|MalaCards C0151825 Ostalgia C3179239 Osteopetrosis autosomal dominant type 2 OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C3810023 Verheij syndrome MalaCards C0036572 Convulsion C0021390 Inflammatory bowel diseases HSDN C4084784 Diarrhea C0795623 Hepatitis a vaccine, inactivated HSDN C0040259 Tinea pedis C0011615 Dermatitis, atopic HSDN C0149793 Transient monocular blindness C1261287 Stenosis HSDN C0002622 Amnesias C0019829 Hodgkin disease HSDN C1135120 Breakthrough pain C0033581 Prostatitis HSDN C0018784 Deafness sensorineural C2748572 Sesame syndrome OrphaNet|HPO C3539895 Pelvic pain occurs with bowel movement C0409354 Flexion contracture of hip HSDN C3641756 Have diarrhea C0162871 Aortic aneurysm, abdominal HSDN C0036572 Convulsion C0024110 Pulmonary abscess HSDN C0036572 Convulsion C1868678 Thanatophoric dysplasia, type i (disorder) MalaCards|HPO C2919142 Short stature adverse event C2930815 Acute cerebral gaucher disease MalaCards C4085548 Usual severity dizziness C0001175 Acquired immunodeficiency syndrome HSDN C0027066 Myoclonic jerking C2678051 Mental retardation, x-linked 94 (disorder) MalaCards|HPO|UMLS C3887784 Decreased urine output C0019050 Hemoglobinuria, paroxysmal HSDN C0344315 Mood depressed C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C4084766 Vomiting C3814778 Hemolytic index HSDN C0242936 Center pain C0015670 Child father HSDN C0042510 Fibrillation paroxysmal vent C3150953 Long qt syndrome 6 MalaCards|HPO C1963281 Vomiting adverse event C1690964 Cataract HSDN C2984057 Have nausea C0040053 Thrombosis HSDN C4042891 Sleep wake disorders C0524528 Pervasive development disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016558 Forensic psychiatri HSDN C0027497 Queasy C3714644 Thymus neoplasms HSDN C2936821 Spinal cerebrospinal fluid leak C0024958 Maxillary sinus neoplasms HSDN C0600142 Flash hot C0038986 Sweat gland diseases HSDN C0018681 Headache, cephalalgia C2984299 Asthma pathway HSDN C1549543 Administration method - pain C0013449 Ear neoplasms HSDN C0000727 Abdomen acute C0031046 Pericarditis HSDN C2024878 Cardiovascular surgery result: dyspnea C0268248 Niemann pick disease, adult non neuronopathic MalaCards|HPO C0000737 Abdomen pain C0015663 Fasting HSDN C0004604 Pain back C0001175 Acquired immunodeficiency syndrome HSDN C0518090 Frequency of pain question C0848377 Trauma to the abdomen HSDN C4084788 Have dizziness C0019069 Hemophilia a HSDN C1963135 Hepatic necrosis adverse event C0854176 Malignant hepato-biliary neoplasm MalaCards C0018681 Headache, cephalalgia C0086774 Cold hemoglobinuria OrphaNet|MalaCards C0012833 Dizzy C0155517 Hypoactive labyrinth-unilat. UMLS C0026838 Spasticity muscle C1865864 Amyotrophic lateral sclerosis 5 MalaCards|HPO|UMLS C2984057 Have nausea C1704972 Genomic orientation HSDN C0011991 Loose stools C0311267 Hill diarrhea UMLS C0015469 Facial paralysis C0034530 Injury radiation HSDN C0242936 Center pain C0342443 Adrenal cushing's syndrome HSDN C0016199 Pain flank C0162283 Nephrogenic diabetes insipidus HSDN C0036572 Convulsion C3809356 Multiple congenital anomalies-hypotonia-seizures syndrome 3 MalaCards|UMLS C0018772 Deafness C0265239 Wildervanck's syndrome MalaCards C0221232 Welts C1274856 Lupus erythematosus-associated urticarial vasculitis UMLS C4084802 Usual severity diarrhea C0424688 Small head HSDN C2237041 Shox gene with short stature C0175699 Saethre-chotzen syndrome MalaCards|HPO C4084774 Have weight loss C0023364 Leptospirosis HSDN C4085862 Bothered by nausea C0012691 Dislocations HSDN C0085606 Urination urgency C1863704 Spastic paraplegia 8, autosomal dominant MalaCards|HPO C1961131 Cough adverse event C0872315 Communicable diseases emerging HSDN C4042891 Sleep wake disorders C0852795 Increased insulin level HSDN C0242936 Center pain C0004940 Behavioral science HSDN C0008031 Pain chest C0008628 Chromosome deletion HSDN C0013604 Edematous C0019372 Herpesviridae infections HSDN C0241137 Skin pallor C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0019572 Hairiness C0024299 Lymphoma HSDN C0595939 Stillborn C0265218 Neu-laxova syndrome HPO C4084784 Diarrhea C0016548 Foreign body migration HSDN C2984057 Have nausea C0038436 Post-traumatic stress disorder HSDN C0024031 Back pain lower back C0019080 Hemorrhage HSDN C1557397 Adverse event associated with pain C0009442 Common bile duct neoplasms HSDN C0041657 Consciousness loss C0413398 Accidental decapitation HSDN C0027497 Queasy C0027873 Neuromyelitis optica MalaCards|HSDN C2315100 Pediatric failure to thrive C1852576 Copper deficiency, familial benign MalaCards C0518090 Frequency of pain question C0013370 Amebic colitis HSDN C0010520 Skin cyanosis C0031090 Periodontal diseases HSDN C0027796 Neuralgias C1963229 Retinal detachment adverse event HSDN C0278152 Hemifacial spasms C0349604 Intracranial meningioma MalaCards C0917816 Deficiency mental C1839125 Say-meyer syndrome MalaCards C0000737 Abdomen pain C3272463 Ampulla of vater undifferentiated carcinoma with osteoclast-like giant cells UMLS C2315100 Pediatric failure to thrive C3150921 Microcephaly, postnatal progressive, with seizures and brain atrophy HPO C0036572 Convulsion C0393484 Rasmussen syndrome UMLS C3815497 Cough C2706915 Language:-:point in time:^patient:- HSDN C0022346 Yellow skin C0033975 Psychotic disorders HSDN C3898969 Have been vomiting C0017574 Gingivitis HSDN C0020903 Illusion C0017601 Glaucomas HSDN C0520909 Ponv C0010054 Coronary arteriosclerosis HSDN C0027796 Neuralgias C0919267 Ovarian neoplasm HSDN C4085317 Diarrhea frequency C0347555 Friction blister HSDN C0022346 Yellow skin C3469186 Hemochromatosis, type 1 HSDN C0036572 Convulsion C0153017 Encephalitis varicella HSDN C3641756 Have diarrhea C0238198 Gastrointestinal stromal tumors HSDN C0497247 Blood pressure elevation C0027831 Neurofibromatosis 1 HPO C0557874 Global developmental delay C3150649 Autoimmune disease, multisystem, with facial dysmorphism MalaCards|HPO C0233775 Hallucination, mood congruent C0018524 Hallucinations UMLS C2237041 Shox gene with short stature C0265499 49,xxxxy chromosomal anomaly MalaCards C4084769 Vomiting frequency C0085298 Sudden cardiac death HSDN C1145670 Failure respiratory C2677099 Crouzon syndrome with acanthosis nigricans (disorder) MalaCards|HPO C0036396 Sciatica C0220847 C hepatitis virus HSDN C1963086 Confusion adverse event C0025284 Meningeal neoplasms HSDN C0013404 Respiratory difficulty C0085083 Ovarian hyperstimulation syndrome HSDN C0042798 Vision dim C0036674 Sensory deprivation HSDN C0015672 Decreased energy C0003962 Ascites HSDN C0030486 Extremity paralysis, lower C3714644 Thymus neoplasms HSDN C1962972 Proteinuria adverse event C0006309 Brucellosis HSDN C1962962 Hyperpigmentation adverse event C0268060 Juvenile hemochromatosis MalaCards C0349588 Stature short C1857052 Ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia OrphaNet|MalaCards C4084725 Usual severity cough C0035412 Rhabdomyosarcoma HSDN C0232462 Appetite decrease C0235974 Pancreatic carcinoma MalaCards C1963281 Vomiting adverse event C0019537 High pressure nervous syndrome HSDN C1963091 Diarrhea adverse event C0553580 Ewings sarcoma HSDN C4085210 Usual severity pain C1548485 Rift valley fever vaccine HSDN C0085593 Chill C0494043 Streptobacillosis MalaCards C1549543 Administration method - pain C0027664 Neoplasms, muscle tissue HSDN C4084723 Constipation C0027765 Nervous system disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0376547 Aromatherapy HSDN C0026821 Cramp C1962963 Osteoporosis adverse event HSDN C0018991 Paralysis one side of body C2350521 Gustatory perception HSDN C0700078 Deep tendon reflex decrease C1847823 Charcot-marie-tooth disease, axonal, type 2f MalaCards|HPO C0009421 Comatose C0272199 Familial hemophagocytic lymphocytosis MalaCards C0162298 Stiffness joints C1706192 Sulfatidosis MalaCards C0041657 Consciousness loss C0039239 Sinus tachycardia HSDN C1549543 Administration method - pain C0085078 Lysosomal storage diseases HSDN C0020538 Hbp C1840391 Pseudohypoaldosteronism, type iic MalaCards C0010200 Cough symptom C3495422 Finding relating to sexuality and sexual activity HSDN C0235153 Sensory hallucination C0029838 Other specified types of schizophrenia MalaCards C0009398 Color vision defects C0027686 Pathologic neovascularization HSDN C3539889 Pelvic pain increasing in severity C1456865 Ureteral calculi HSDN C2024893 Cardiovascular surgery result: fatigue C0036341 Schizophrenia HSDN C0019572 Hairiness C0460137 Push down or depress HSDN C1955517 Dysphagia, pharyngoesophageal phase C0810319 Other and unspecified gastrointestinal disorders UMLS C0030486 Extremity paralysis, lower C0021361 Female infertility HSDN C0034933 Abnormal reflexes C0029124 Optic atrophy HSDN C0027497 Queasy C1546654 Specimen source codes - granuloma HSDN C0027497 Queasy C0025007 Measles HSDN C1999266 Depression adverse event C3280358 Wolfram-like syndrome, autosomal dominant OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C2749484 Neuroblastoma, susceptibility to HPO C0030486 Extremity paralysis, lower C1546949 Event consequence - death HSDN C4085210 Usual severity pain C0002940 Aneurysm HSDN C1963087 Constipation adverse event C0268322 Chester-type porphyria HPO C4084784 Diarrhea C0011071 Sudden death HSDN C0398650 Idiopathic thrombocytopenia purpura C0015231 Exanthem subitum HSDN C1963087 Constipation adverse event C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0271215 Blindness legal C0349604 Intracranial meningioma MalaCards C0026821 Cramp C0009492 Compartment syndromes HSDN C0751495 Seizure focal C0393722 Eyelid myoclonus with absences UMLS C0026884 Muteness C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C0030193 Sense of pain C0043255 Stab wound HSDN C0085636 Light sensitivity C0022593 Keratosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027873 Neuromyelitis optica HSDN C1963071 Back pain adverse event C0850803 Anaphylaxis (non medication) HSDN C1961131 Cough adverse event C3887588 Tracheopathia osteoplastica MalaCards C4085211 Pain distress question C0029442 Osteomalacia HSDN C0332566 Maculopapule C0343836 Achromic skin lesions of carate UMLS C3815497 Cough C1527406 Rhizomelic pseudopolyarthritis MalaCards C1963281 Vomiting adverse event C2936913 Porphyria, south african type HPO C0027498 Nausea vomiting C1264008 Chronic cold agglutinin disease MalaCards C0020903 Illusion C0349231 Phobic anxiety disorder HSDN C0231807 Dyspnea exertional C0155567 Rheumatic aortic obstruction MalaCards C0018808 Murmur C0007137 Squamous cell carcinoma HSDN C2911647 Weight gain adverse event C0018799 Heart diseases HSDN C3539022 Pelvic pain decreasing in severity C1881674 Medical device emits smoke HSDN C1384666 Decreased hearing C0011168 Deglutition disorders HSDN C0018772 Deafness C0034139 Purine-pyrimidine metabolism, inborn errors HSDN C0037771 Paraparesis spastic C0038379 Eye deviation HSDN C4084788 Have dizziness C0033860 Psoriasis HSDN C2984057 Have nausea C0027092 Myopia HSDN C0013604 Edematous C0035579 Rickets HSDN C0557874 Global developmental delay C0265303 Acrocephalopolysyndactyly type iv MalaCards C0027497 Queasy C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0009806 Constipate C0038395 Streptococcal infections HSDN C0522224 Palsied C0005974 Bone resorption HSDN C3274924 Have been coughing C0037933 Spinal diseases HSDN C3463815 Feel fatigue C0018939 Hematological disease HSDN C0242936 Center pain C0020598 Hypocalcemia HSDN C3641756 Have diarrhea C0004144 Atelectasis HSDN C0023012 Delay language C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C4085317 Diarrhea frequency C0016397 Focal infection HSDN C0085631 Abnormal excitement C0038160 Staphylococcal infections HSDN C2919142 Short stature adverse event C1858656 Short stature, idiopathic, autosomal MalaCards C2984057 Have nausea C0004935 Animal ethology HSDN C4084774 Have weight loss C0037356 Smallpox virus HSDN C3463815 Feel fatigue C0018824 Heart valve disease HSDN C4085210 Usual severity pain C0035579 Rickets HSDN C0557874 Global developmental delay C3160739 Fanconi anemia, complementation group e MalaCards C0242670 Chronic vegetative state C0428953 Ecg infarction myocardial HSDN C0557874 Global developmental delay C3280856 Ichthyosis, spastic quadriplegia, and mental retardation MalaCards C0013604 Edematous C0542428 Hypochondrogenesis HPO C2911645 Weight loss adverse event C0151744 Myocardial ischemia HSDN C0151786 Weakness muscle C0023788 Whipple disease MalaCards C3665347 Vision impaired C1853925 Spondyloocular syndrome, autosomal recessive OrphaNet|HPO|MalaCards C0242936 Center pain C0024689 Mandibular diseases HSDN C0030193 Sense of pain C0040820 Trematode infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0012644 Animal disease models HSDN C0027497 Queasy C2240378 Cleft palate on exam HSDN C0398650 Idiopathic thrombocytopenia purpura C0006663 Calcinosis HSDN C0013911 Emaciate C2911643 Encounter due to family history of osteoporosis HSDN C0751837 Gait ataxic C1837541 Spinocerebellar ataxia 20 MalaCards|UMLS C1963071 Back pain adverse event C2678055 Myopathy, x-linked, with postural muscle atrophy (disorder) MalaCards|HPO C0518090 Frequency of pain question C0020258 Hydrocephalus, normal pressure HSDN C2700617 Irritation - emotion C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) HPO C0009763 Conjunctiva inflammation C0162361 Hidrotic ectodermal dysplasia HPO C4085211 Pain distress question C1532253 Sedentary lifestyle HSDN C1963137 Hydrocephalus adverse event C0349604 Intracranial meningioma MalaCards C1963247 Ventricular tachycardia adverse event C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) OrphaNet|HPO|MalaCards C0036396 Sciatica C0030100 Oxyuriasis HSDN C1963249 Tinnitus adverse event C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0042571 Vertigo subjective C0752143 Intracranial thrombosis HSDN C1963093 Dizziness adverse event C0013990 Pathological accumulation of air in tissues HSDN C4042891 Sleep wake disorders C0027562 Negativism HSDN C0497247 Blood pressure elevation C2931667 Fitzsimmons walson mellor syndrome MalaCards C4084767 Bothered by vomiting C0751161 Udpglucose 4-epimerase deficiency disease MalaCards|HPO C1384666 Decreased hearing C0032453 Polychondritis, relapsing HSDN C0014089 Functional encopresis C3244301 Coverage level - family HSDN C3539896 Pelvic pain occurs with urination C0037051 Behavior illness HSDN C0011991 Loose stools C0028077 Night blindness HSDN C0004134 Dyssynergia C1857355 Leigh syndrome , french canadian type HPO|UMLS C1557397 Adverse event associated with pain C0206754 Neuroendocrine tumors HSDN C0030193 Sense of pain C0025292 Haemophilus meningitis HSDN C0015469 Facial paralysis C0030567 Parkinson disease HSDN C0024032 Birth weight subnormal C1857556 Hsd11b2, arg208his HPO C0007758 Cerebellar ataxia C0041327 Tuberculosis, pulmonary HSDN C0034933 Abnormal reflexes C0017178 Gastrointestinal diseases HSDN C0013604 Edematous C0520679 Sleep apnea, obstructive HSDN C0043094 Weight gain C0002726 Amyloidosis HSDN C0522224 Palsied C0041755 Adverse reaction to drug HSDN C1963065 Apnea adverse event C0151740 Intracranial hypertension HSDN C0023015 Language handicap C0023448 Lymphoid leukemia HSDN C0008031 Pain chest C1332511 Benign germ cell neoplasm of mediastinum UMLS C4085862 Bothered by nausea C3812171 Bradycardia by ecg finding HSDN C0151686 Growth retardation C3554129 Combined oxidative phosphorylation deficiency 13 MalaCards C0042024 Urine incontinence C0017416 Genital neoplasms, female HSDN C0018784 Deafness sensorineural C1864815 Deafness, autosomal recessive 46 (disorder) MalaCards C4085210 Usual severity pain C0018818 Ventricular septal defects HSDN C1549543 Administration method - pain C0018023 Nodular goiter HSDN C3539891 Pelvic pain to the rear C0017638 Glioma HSDN C4085210 Usual severity pain C0041408 Turner syndrome HSDN C0020580 Decreased sensation C0740392 Infarction, middle cerebral artery HSDN C0030552 Paralysis partial C1135841 Zoster sine eruptione HSDN C4084784 Diarrhea C0008733 Chylothorax HSDN C0522224 Palsied C0032964 Pregnancy complications, hematologic HSDN C0018784 Deafness sensorineural C0027720 Nephrosis HSDN C3146279 Coma C0677607 Hashimoto disease HSDN C1549543 Administration method - pain C0037019 Shy-drager syndrome HSDN C0015672 Decreased energy C0004238 Atrial fibrillation HSDN C0033377 Caudal displacement C0268338 Ehlers-danlos syndrome, type iv HPO C0042963 Symptoms vomiting C1705810 Generic role HSDN C4084768 Usual severity vomiting C0342701 Transcobalamin ii deficiency MalaCards C4084723 Constipation C0027947 Neutropenia HSDN C4085210 Usual severity pain C0007798 Cerebral ventricle neoplasm HSDN C4085211 Pain distress question C2936350 Plaque, atherosclerotic HSDN C0012833 Dizzy C0000735 Abdominal neoplasms HSDN C4085211 Pain distress question C0005604 Trauma birth HSDN C0013404 Respiratory difficulty C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C0030193 Sense of pain C0038018 Spondylolysis HSDN C4084769 Vomiting frequency C0017416 Genital neoplasms, female HSDN C0013421 Dystonia C0154723 Migraine with aura HSDN C0427190 Ataxia, truncal C3280692 Mchccd MalaCards|UMLS C1279888 Proteinuria of undiagnosed cause C0027663 Neoplasms, multiple primary HSDN C0234376 Tremor action C0025149 Medulloblastoma MalaCards C0004134 Dyssynergia C1849322 Sandhoff disease, infantile type HPO C0727671 Red cross toothache drops C0001418 Adenocarcinoma HSDN C0015672 Decreased energy C3809991 Immunodeficiency, common variable, 10 MalaCards C0557874 Global developmental delay C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C4085211 Pain distress question C0020523 Immediate hypersensitivity HSDN C0015799 Feminisation C0008497 Choriocarcinoma HSDN C4084726 Distress cough C0020542 Pulmonary hypertension HSDN C0018772 Deafness C0023676 Life style HSDN C1384666 Decreased hearing C0002871 Anemia HSDN C0851578 Disorder sleep C0009404 Colorectal neoplasms HSDN C4085210 Usual severity pain C0039130 Cardiovascular syphilis HSDN C2024878 Cardiovascular surgery result: dyspnea C3244301 Coverage level - family HSDN C0497247 Blood pressure elevation C0268425 Alstrom syndrome MalaCards|HPO C0423823 Nail thinness C1860823 Trichorhinophalangeal syndrome, type iii MalaCards C0011991 Loose stools C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0427055 Face weakness C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0085631 Abnormal excitement C0152054 Therapeutic touch HSDN C1962972 Proteinuria adverse event C0022876 Premature obstetric labor HSDN C0036572 Convulsion C1832814 Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant MalaCards C4084769 Vomiting frequency C1866495 Bartter syndrome, antenatal type 1 HPO C0003469 Anxiety disorder C1855606 Burton syndrome MalaCards C0085606 Urination urgency C3160917 Bladder pain syndrome OrphaNet|MalaCards C0031911 Pigment deposition C0014145 Yolk sac tumor MalaCards C0027498 Nausea vomiting C0003123 Anorexia UMLS C0030552 Paralysis partial C0024530 Malaria HSDN C2024893 Cardiovascular surgery result: fatigue C2609414 Acute kidney injury HSDN C0039070 Collapse fleeting C0014547 Epilepsies, partial HSDN C4084774 Have weight loss C0086768 Pancreatic cholera OrphaNet|MalaCards C0277959 Hair coarseness C1859252 Cerebrofaciothoracic dysplasia OrphaNet|HPO|MalaCards C1963247 Ventricular tachycardia adverse event C3150754 Glycogen storage disease xv MalaCards C2237041 Shox gene with short stature C0268242 Niemann-pick disease, type a MalaCards|HPO C0518090 Frequency of pain question C0015461 Facial neoplasms HSDN C0700078 Deep tendon reflex decrease C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards|HPO C0587048 Upper extremity mass C0343231 Wrist ganglion cyst UMLS C4085317 Diarrhea frequency C0021364 Male infertility HSDN C0043094 Weight gain C0018099 Gout HSDN C0009421 Comatose C0042024 Urinary incontinence HSDN C1557397 Adverse event associated with pain C0032780 Postmortem changes HSDN C1963086 Confusion adverse event C1963198 Pancreatitis adverse event HSDN C0557874 Global developmental delay C2936862 Bardet-biedl syndrome 1 (disorder) MalaCards C1962972 Proteinuria adverse event C0007570 Celiac disease HSDN C0013421 Dystonia C1962983 Cataract adverse event HSDN C0017565 Gingiva hemorrhage C0398650 Immune thrombocytopenic purpura MalaCards|HSDN|HPO C0007758 Cerebellar ataxia C0343108 Flynn aird syndrome OrphaNet|MalaCards C4084769 Vomiting frequency C0014170 Endometrial neoplasms HSDN C0011991 Loose stools C0022890 Labyrinthine disorder HSDN C2132198 Abnormal blistering of the skin C0392436 Pemphigus, benign MalaCards C0019079 Bloody sputum C1710173 Squamous cell lung carcinoma, basaloid variant UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C0009324 Ulcerative colitis HSDN C3641755 Have constipation C0233629 Thinking and speaking disturbances HSDN C1000483 Genus anemia C0268251 Gaucher disease, type 3 (disorder) OrphaNet|HPO|MalaCards C0700078 Deep tendon reflex decrease C0752353 Atrophy, muscular, spinobulbar OrphaNet|HPO C0040259 Tinea pedis C0276758 Fusarium infection HSDN C0030552 Paralysis partial C0860603 Anxiety symptoms HSDN C3665347 Vision impaired C1837073 Spondylometaphyseal dysplasia with cone-rod dystrophy OrphaNet|HPO C3274924 Have been coughing C0206629 Pulmonary blastoma OrphaNet|HSDN|MalaCards C0019209 Large liver C0036920 Sezary syndrome OrphaNet|HPO|MalaCards C0009806 Constipate C1548578 Location characteristic id - smoking HSDN C0040485 Wryneck C0432062 Contracture of sternomastoid UMLS C0036572 Convulsion C0270327 Bedwetting HSDN C0002962 Angina C0003125 Anorexia nervosa HSDN C4084774 Have weight loss C3665624 Serum calcium below normal HSDN C0018784 Deafness sensorineural C0030920 Peptic ulcer HSDN C4084802 Usual severity diarrhea C0029295 Oropharyngeal neoplasms HSDN C1963093 Dizziness adverse event C1306759 Eosinophilic disorder HSDN C3641755 Have constipation C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0033941 Psychoses, substance-induced HSDN C0221752 Rbc urine C1956391 Temporal arteritis MalaCards|HPO C3898969 Have been vomiting C0013182 Drug allergy HSDN C0013604 Edematous C0559260 Congenital scoliosis HSDN C0007758 Cerebellar ataxia C1962986 Glaucoma adverse event HSDN C2029884 Hearing loss by exam C0003864 Arthritis HSDN C2911645 Weight loss adverse event C0014858 Esophageal motility disorders HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0023798 Lipoma HSDN C0042024 Urine incontinence C0014170 Endometrial neoplasms HSDN C0853986 Lymphocytes decreased C3809768 Immunodeficiency 13 MalaCards C0009421 Comatose C0020255 Hydrocephalus HSDN C0030193 Sense of pain C0014553 Absence epilepsy HSDN C3539890 Pelvic pain causes awakening at night C0009373 Colonic diseases HSDN C0036572 Convulsion C0017412 Genital diseases, male HSDN C0018808 Murmur C0002949 Aneurysm, dissecting HSDN C0004604 Pain back C0007194 Hypertrophic cardiomyopathy HSDN C0020673 Hypothermia (central) (local) C0878544 Cardiomyopathies HSDN C3539892 Pelvic pain in front C0001624 Adrenal gland neoplasms HSDN C0010520 Skin cyanosis C0424688 Small head HSDN C0917816 Deficiency mental C0034345 Pyruvate dehydrogenase complex deficiency disease MalaCards|HPO C0497406 Over weight C0027643 Neoplasm recurrence, local HSDN C0242936 Center pain C0016412 Folic acid deficiency HSDN C3274924 Have been coughing C0023869 Lithiasis HSDN C0009806 Constipate C2711227 Steatohepatitis HSDN C0042963 Symptoms vomiting C0018571 Hand injury HSDN C4084726 Distress cough C1623041 Breast-fed HSDN C0460137 Push down or depress C1970035 Parkinson disease 6, late-onset, susceptibility to HPO C0019572 Hairiness C0795843 12 ring syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0151814 Coronary occlusion HSDN C0036572 Convulsion C0034186 Pyelonephritis HSDN C0015672 Decreased energy C0006277 Bronchitis HSDN C0150055 Pain chronic C0236969 Substance-related disorders HSDN C4084768 Usual severity vomiting C0017152 Gastritis HSDN C0017181 Gastrointestinal bleed C2939462 Immunoglobulin deposition disease MalaCards C0413252 Hypothermia due to exposure C0002949 Aneurysm, dissecting HSDN C3463815 Feel fatigue C0020255 Hydrocephalus HSDN C1963087 Constipation adverse event C0019270 Hernia HSDN C0151311 Cranial nerve palsy C0221060 Mobius syndrome OrphaNet|MalaCards C0013362 Dysarthrias C2746067 Spinocerebellar ataxia 22 HPO C0004604 Pain back C0037051 Behavior illness HSDN C0018524 Hallucinate C0030567 Parkinson disease MalaCards C0271215 Blindness legal C0268281 Infantile neuronal ceroid lipofuscinosis OrphaNet|HPO|MalaCards C0026826 High muscle tone C1968551 Mental retardation, x-linked 79 MalaCards C0037199 Sinus infection C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C2237041 Shox gene with short stature C1135161 Stage 4s neuroblastoma MalaCards C1000483 Genus anemia C0043207 Wolfram syndrome MalaCards|HPO C0917816 Deficiency mental C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria MalaCards C0264602 Spastic pseudobulbar dysphonia C0264603 Mixed flaccid-spastic pseudobulbar dysphonia UMLS C0426579 Anorexia symptom C0042847 Vitamin b 12 deficiency HSDN C0522224 Palsied C1963064 Anxiety adverse event HSDN C0085632 Listlessness C1847967 Ovarioleukodystrophy MalaCards C0019209 Large liver C0085253 Adult-onset still disease OrphaNet|MalaCards C2029884 Hearing loss by exam C0039131 Syphilis congenital HSDN C1549543 Administration method - pain C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0015970 Fever unknown origin C0037889 Hereditary spherocytosis HSDN C0151827 Pain eye C0010035 Hereditary corneal dystrophy HSDN C0037384 Snore C0812393 Cancer patients and suicide and depression HSDN C4085210 Usual severity pain C0005716 Blastomycosis HSDN C0349588 Stature short C3468041 Fanconi anemia, complementation group c MalaCards C3641755 Have constipation C0021295 Infant, premature, diseases HSDN C0020673 Hypothermia (central) (local) C0002063 Alkalosis HSDN C0518090 Frequency of pain question C0037023 Sialadenitis HSDN C0349588 Stature short C3279941 Stickler syndrome, type iv MalaCards C0013404 Respiratory difficulty C1999266 Depression adverse event HSDN C0011168 Disorder deglutition C0268242 Niemann-pick disease, type a MalaCards C0000737 Abdomen pain C1519371 Small intestinal eatl UMLS C4085317 Diarrhea frequency C0021799 Interprofessional relations HSDN C0028738 Nystagmus C0342684 Ocular albinism, type i OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0162429 Malnutrition HSDN C0004134 Dyssynergia C0038356 Stomach neoplasms HSDN C3203358 Alveolar hypoventilation C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0233844 Awkwardness C1869123 Limb-girdle muscular dystrophy type 2a MalaCards|HPO C0424755 Fever symptoms C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0003862 Pain joint C0018801 Heart failure HSDN C1279888 Proteinuria of undiagnosed cause C0011615 Dermatitis, atopic HSDN C0426579 Anorexia symptom C2219717 Menstrual periods stopped for over 6 months HSDN C0019079 Bloody sputum C1266035 Bronchiolo-alveolar carcinoma, mucinous UMLS C0038002 Spleen enlargement C1835931 Alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity OrphaNet|HPO|MalaCards C0009806 Constipate C3897085 Stage iic colon cancer UMLS C0012833 Dizzy C0032453 Polychondritis, relapsing OrphaNet|MalaCards C4084774 Have weight loss C0021603 Sleep initiation and maintenance disorders HSDN C0036572 Convulsion C1332308 Anterior optic tract meningioma UMLS C0007758 Cerebellar ataxia C1145670 Respiratory failure HSDN C3815497 Cough C0149721 Left ventricular hypertrophy HSDN C0003550 Broca aphasia C0752140 Intracranial embolism HSDN C0016199 Pain flank C1512750 Infiltrating renal pelvis and ureter transitional cell carcinoma UMLS C0237326 Defecation pain C2931518 Plexosarcoma MalaCards C0030552 Paralysis partial C0027859 Acoustic neuroma HSDN C0151889 Reflexes tendon increased C1291386 D-glycericacidemia MalaCards|HPO C0795692 Lactate blood increased C0019209 Hepatomegaly HSDN C4084775 Usual severity weight loss C0024110 Pulmonary abscess HSDN C0018926 Emesis bloody C0020532 Hypersplenism HSDN C2237041 Shox gene with short stature C2931588 Gemss syndrome OrphaNet|HPO|MalaCards C0850758 Pain pelvic C2911643 Encounter due to family history of osteoporosis HSDN C2984058 Have pain C0009442 Common bile duct neoplasms HSDN C3665492 Pigmentations C0751593 Cancer, infratentorial MalaCards C0030193 Sense of pain C0024954 Maxillary neoplasms HSDN C4085211 Pain distress question C0024950 Maxillary diseases HSDN C0015469 Facial paralysis C0085423 Gram-negative bacterial infections HSDN C0085636 Light sensitivity C0339537 Cone monochromatism MalaCards|HPO|UMLS C0009421 Comatose C0268543 Hyperammonemia, type iii MalaCards|HPO C0018784 Deafness sensorineural C0022353 Neonatal jaundice HSDN C3665492 Pigmentations C0007102 Malignant tumor of colon MalaCards C0003962 Ascites C2931878 Familial primary biliary cirrhosis MalaCards C0007758 Cerebellar ataxia C1848070 Lissencephaly and agenesis of corpus callosum HPO C0235299 Abdomen ruq pain C0019158 Hepatitis UMLS C0242936 Center pain C0520459 Necrotizing enterocolitis HSDN C0151686 Growth retardation C0220754 Biotinidase deficiency MalaCards|HPO C4085862 Bothered by nausea C0162820 Dermatitis, allergic contact HSDN C1963087 Constipation adverse event C0005974 Bone resorption HSDN C0002962 Angina C0011581 Depressive disorder HSDN C0151786 Weakness muscle C0007279 Carotid body paraganglioma HSDN C0031911 Pigment deposition C0001418 Adenocarcinoma MalaCards C3829611 Nausea frequency C0003486 Aortic aneurysm HSDN C0393903 Leg moving painful toe C0393901 Disorders of spinal neurones manifest by hyperactivity UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C2609059 Antisynthetase syndrome OrphaNet|MalaCards C0162298 Stiffness joints C3536983 Familial hypophosphatemic rickets OrphaNet C4084775 Usual severity weight loss C4045991 Perihilar cholangiocarcinoma MalaCards C4085317 Diarrhea frequency C0273486 Cranial nerve x injury HSDN C0012569 Double vision C0520719 Spinopontine atrophy MalaCards C0009763 Conjunctiva inflammation C0153257 Coccidioidomycosis primary pulmonary MalaCards C0026838 Spasticity muscle C4225276 Epilepsy, hearing loss, and mental retardation syndrome UMLS C1963281 Vomiting adverse event C0002991 Cutaneous fibrous histiocytoma HSDN C1557397 Adverse event associated with pain C0018671 Head and neck neoplasms HSDN C4084776 Weight loss C0850803 Anaphylaxis (non medication) HSDN C0009806 Constipate C0025202 Melanoma HSDN C0007758 Cerebellar ataxia C0398367 Histiocytic necrotizing lymphadenitis MalaCards C4085210 Usual severity pain C0043167 Pertussis HSDN C0015938 Fetal macrosomia C0018802 Congestive heart failure HSDN C0004134 Dyssynergia C2931925 Abetalipoproteinemia neuropathy MalaCards C4084723 Constipation C0008149 Chlamydia infections HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1856403 Etfb deficiencies HPO C0085631 Abnormal excitement C0040517 Gilles de la tourette syndrome HSDN C0030193 Sense of pain C0012243 Digestive system neoplasms HSDN C4085211 Pain distress question C0008495 Chorioamnionitis HSDN C2024878 Cardiovascular surgery result: dyspnea C3810814 Myocardial infarction ecg assessment HSDN C0221150 Odynophagia C0011168 Deglutition disorders UMLS C0013595 Eczematous dermatitis C0406555 Elastoderma MalaCards C0010200 Cough symptom C1708781 Lung sarcomatoid carcinoma UMLS C4050613 Anxiety C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C0005745 Blepharoptosis C1306794 Wound botulism OrphaNet|MalaCards C0015672 Decreased energy C0153653 Malignant tumor of parathyroid gland MalaCards C0009398 Color vision defects C0003873 Rheumatoid arthritis HSDN C0000737 Abdomen pain C0037051 Behavior illness HSDN C0004134 Dyssynergia C1876161 Ceroid lipofuscinosis, neuronal, 2 MalaCards|HPO|UMLS C0007758 Cerebellar ataxia C0268542 Ornithine carbamoyltransferase deficiency HSDN C0037317 Sleep disturbance C2748910 Rett syndrome, atypical MalaCards C0242936 Center pain C1522137 Hypertriglyceridemia result HSDN C0036572 Convulsion C0004030 Aspergillosis HSDN|UMLS C0007758 Cerebellar ataxia C0036341 Schizophrenia HSDN C0234144 Dysgraphia C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0004352 Autistic disorder HSDN C0018772 Deafness C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C1260880 Nasal drip C0278952 Nasopharyngeal cancer recurrent UMLS C0518090 Frequency of pain question C0035439 Rheumatic heart disease HSDN C0237326 Defecation pain C3280479 Pitt-hopkins-like syndrome 2 MalaCards C0036572 Convulsion C1846057 Armfield x-linked mental retardation syndrome OrphaNet|UMLS|MalaCards C0007758 Cerebellar ataxia C2931842 Diaphyseal dysplasia 1, progressive MalaCards C0349506 Sun sensitivity C1970808 Xeroderma pigmentosum b-cockayne syndrome HPO C1963065 Apnea adverse event C0700359 Organophosphate poisoning HSDN C0917816 Deficiency mental C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0038990 Sweats C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C4084767 Bothered by vomiting C0033871 Psychiatric status rating scales HSDN C1999266 Depression adverse event C0268425 Alstrom syndrome MalaCards|HPO C0022408 Disorder joint C1261128 Progeria-like syndrome MalaCards C4085211 Pain distress question C0035372 Rett syndrome HSDN C1963281 Vomiting adverse event C0338437 Neurocysticercosis HSDN C0015970 Fever unknown origin C0025229 Melioidosis HSDN C0018784 Deafness sensorineural C0035923 German measles vaccine HSDN C4084802 Usual severity diarrhea C0018133 Graft-vs-host disease HSDN C0030193 Sense of pain C0009081 Congenital clubfoot HSDN C0575081 Abnormal gait C0023931 Lobstein's disease OrphaNet C2984058 Have pain C0021308 Infarction HSDN C0221232 Welts C1274932 Drug-induced serum sickness UMLS C0042963 Symptoms vomiting C3714509 Nutrition disorders HSDN C0020673 Hypothermia (central) (local) C0014859 Esophageal neoplasms HSDN C0037316 Not enough sleeping C0033046 Premenstrual syndrome HSDN C4084769 Vomiting frequency C0014869 Peptic esophagitis HSDN C0003469 Anxiety disorder C1864851 Pigmented nodular adrenocortical disease, primary, 2 HPO C0042963 Symptoms vomiting C1855115 Methylmalonic aciduria, mut(0) type HPO C0026821 Cramp C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0085635 Flash light C0346373 Malignant melanoma of iris HPO C2024893 Cardiovascular surgery result: fatigue C0017563 Gingival diseases HSDN C4042891 Sleep wake disorders C1881674 Medical device emits smoke HSDN C3641756 Have diarrhea C1833053 Proprotein convertase 1 3 deficiency HPO C0917816 Deficiency mental C0023138 Laurence-moon syndrome OrphaNet|HPO|MalaCards C3146279 Coma C1855109 Methylmalonic aciduria cbla type HPO C0557874 Global developmental delay C3495427 Fanconi-bickel syndrome MalaCards C0040034 Thrombocytopenia C0751779 Action myoclonus-renal failure syndrome HPO C4085210 Usual severity pain C0041971 Tumor urethra HSDN C0398650 Idiopathic thrombocytopenia purpura C3266026 Autoimmune polyendocrine syndrome type 4 MalaCards C2141063 Dry left eye C0043349 Xerophthalmia UMLS C0027796 Neuralgias C0034040 Puerperal disorders HSDN C0011991 Loose stools C0080178 Spina bifida HSDN C0030193 Sense of pain C0039336 Gustatory sense HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0038833 Superior vena cava syndrome HSDN C0007758 Cerebellar ataxia C1859569 Bardet-biedl syndrome 11 HPO C2315100 Pediatric failure to thrive C3553230 Congenital disorder of glycosylation, type iil MalaCards C4084788 Have dizziness C0027804 Fatigue neurosis HSDN C4085222 Nausea C0018273 Growth disorders HSDN C0413252 Hypothermia due to exposure C1306759 Eosinophilic disorder HSDN C2911645 Weight loss adverse event C0085298 Sudden cardiac death HSDN C0015468 Face pain C0025235 Melkersson-rosenthal syndrome HSDN C0233514 Behavior abnormal C3541340 Pontine tegmental cap dysplasia MalaCards C0038002 Spleen enlargement C1850363 Niemann-pick disease, nova scotian type HPO C0020672 Body temperature decreased C1563716 Thyroid dysgenesis HPO C0018784 Deafness sensorineural C0015934 Fetal growth retardation HSDN C0022638 Ketosis C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C0013604 Edematous C0020120 Engineering humans HSDN C3463815 Feel fatigue C0013481 Ebstein anomaly OrphaNet|HPO|MalaCards C0030193 Sense of pain C0206655 Alveolar rhabdomyosarcoma HSDN C0233480 Hyperirritability C0004943 Behcet syndrome MalaCards C1557397 Adverse event associated with pain C0007095 Carcinoid tumor HSDN C0008031 Pain chest C0079218 Fibromatosis, aggressive MalaCards|HPO C0231835 Respiration rate increased C0018378 Guillain-barre syndrome HSDN C0009806 Constipate C0848377 Trauma to the abdomen HSDN C0042024 Urine incontinence C1546602 Specimen source codes - diverticulum HSDN C0013362 Dysarthrias C3164344 Adult onset autosomal dominant leukodystrophy HPO C4085548 Usual severity dizziness C4050613 Anxiety scale (basc-2) HSDN C1963252 Tremor adverse event C0039494 Temporomandibular joint disorders HSDN C0030232 Color loss C0023381 Letterer-siwe disease MalaCards C4085210 Usual severity pain C0032461 Polycythemia HSDN C0242936 Center pain C0155490 Middle ear cholesteatoma HSDN C0518090 Frequency of pain question C1546949 Event consequence - death HSDN C0038002 Spleen enlargement C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C1565249 Limitation, mobility C3495422 Finding relating to sexuality and sexual activity HSDN C1549543 Administration method - pain C0017574 Gingivitis HSDN C1963063 Anorexia adverse event C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C0015468 Face pain C0016542 Foreign body HSDN C0917816 Deficiency mental C0009207 Cockayne syndrome OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0062527 Hepatitis b vaccine HSDN C2024893 Cardiovascular surgery result: fatigue C0001314 Acute disease HSDN C0003862 Pain joint C0034931 Reflex sympathetic dystrophy HSDN C3827868 Tachycardia by ecg finding C0342859 Harderoporphyria HPO C4084725 Usual severity cough C0037304 Skull fracture HSDN C0042928 Paralysis vocal cord C0020255 Hydrocephalus HSDN C0004604 Pain back C0009244 Behavioral cognitive therapy HSDN C4084802 Usual severity diarrhea C1443900 Inhalational botulism OrphaNet|MalaCards C1557397 Adverse event associated with pain C2931642 Benign symmetrical lipomatosis HSDN C4042891 Sleep wake disorders C0036202 Sarcoidosis HSDN C4084784 Diarrhea C0020452 Hyperemia HSDN C2029884 Hearing loss by exam C0008928 Cleidocranial dysplasia HSDN C0221166 Paraparesis C0018944 Hematoma HSDN C0000737 Abdomen pain C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0018681 Headache, cephalalgia C0017536 Giardiasis HSDN C2237041 Shox gene with short stature C1300260 Spondylar and nasal alterations with striated metaphyses OrphaNet|MalaCards C0030193 Sense of pain C0269103 Endometriosis, implanted UMLS C0023380 Lethargy C0023264 Leigh disease HSDN C0022346 Yellow skin C0275148 Poisoning of animal by plant HSDN C0851578 Disorder sleep C0021400 Influenza HSDN C2984058 Have pain C0029376 Osgood schlatter disease HSDN C2911647 Weight gain adverse event C1253943 Fluid in the chest HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085632 Apathy HSDN C0031256 Petechia C3150315 Aicardi-goutieres syndrome 1, autosomal dominant HPO C0013604 Edematous C0020162 Humerus fracture HSDN C0878773 Bladder hyperactive C0030481 Tropical spastic paraparesis HSDN C0030552 Paralysis partial C0267171 Idiopathic gastric stasis UMLS C0031911 Pigment deposition C0038356 Stomach neoplasms MalaCards C0018775 Hearing loss bilateral C0007785 Cerebral infarction HSDN C0030193 Sense of pain C0477374 Other specified headache syndromes UMLS C0151889 Reflexes tendon increased C0017083 Gangliosidoses MalaCards C3829611 Nausea frequency C0242383 Age related macular degeneration HSDN C1279888 Proteinuria of undiagnosed cause C0242994 Hantavirus infections HSDN C0232943 Metromenorrhagia C0019080 Hemorrhage UMLS C4084774 Have weight loss C0344435 Ventricular fibrillation by ecg finding HSDN C3815497 Cough C0004031 Aspergillosis, allergic bronchopulmonary DiseaseOntology|OrphaNet|MalaCards C0010200 Cough symptom C0017416 Genital neoplasms, female HSDN C0033774 Skin pruritus C1274904 Pruritus due to systemic disorder UMLS C3898969 Have been vomiting C0520799 Acute radiation syndrome HSDN C4084773 Bothered by weight gain C0026896 Myasthenia gravis HSDN C1963091 Diarrhea adverse event C0018824 Heart valve disease HSDN C4085317 Diarrhea frequency C0795956 Chylomicron retention disease MalaCards|HPO C1963091 Diarrhea adverse event C1865373 Severe combined immunodeficiency, partial HPO C0012833 Dizzy C1548578 Location characteristic id - smoking HSDN C0004134 Dyssynergia C2931765 Furukawa takagi nakao syndrome OrphaNet|MalaCards C0036572 Convulsion C1843852 Spinocerebellar ataxia with epilepsy HPO C4084774 Have weight loss C0948089 Acute coronary syndrome HSDN C3539891 Pelvic pain to the rear C0037072 Diseases sigmoid HSDN C3539022 Pelvic pain decreasing in severity C2984291 Glioblastoma multiforme pathway HSDN C0518090 Frequency of pain question C0030581 Parotid neoplasms HSDN C0020903 Illusion C0002395 Alzheimer's disease HSDN C0042963 Symptoms vomiting C1546847 Entity name part type - family HSDN C3463815 Feel fatigue C0041296 Tuberculosis OrphaNet|HPO C0231528 Muscle pain generalized C0162531 Hereditary coproporphyria OrphaNet|HPO C1963071 Back pain adverse event C0008487 Chordoma HSDN C0026821 Cramp C1970820 Fabry disease, cardiac variant HPO C0030486 Extremity paralysis, lower C0078981 Arachnoid cysts HSDN C0460137 Push down or depress C3888102 Frontotemporal dementia with motor neuron disease MalaCards C4085211 Pain distress question C1546949 Event consequence - death HSDN C0700078 Deep tendon reflex decrease C1832274 Charcot-marie-tooth disease, type 2d HPO C0005745 Blepharoptosis C1864233 Endplate acetylcholinesterase deficiency (disorder) MalaCards|HPO C0018681 Headache, cephalalgia C0085183 Neoplasms, second primary HSDN C0413252 Hypothermia due to exposure C0314657 Genetic predisposition HSDN C1963071 Back pain adverse event C0340629 Aortic aneurysm without mention of rupture nos HSDN C0013390 Cramps menstrual C0040053 Thrombosis HSDN C0234376 Tremor action C1834711 Cerebelloparenchymal disorder vi MalaCards|HPO C4085317 Diarrhea frequency C0019054 Hemolysis (disorder) HSDN C0085631 Abnormal excitement C0019537 High pressure nervous syndrome HSDN C0013362 Dysarthrias C0041296 Tuberculosis HSDN C0030193 Sense of pain C0564774 Dysmenorrhea - non-psychogen UMLS C3539020 Pelvic pain decreasing in frequency C0035358 Retroperitoneal neoplasm HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0032453 Polychondritis, relapsing HSDN C0497406 Over weight C0021818 Intervertebral disk displacement HSDN C0002965 Crescendo angina C0035078 Kidney failure HSDN C0033774 Skin pruritus C0037933 Spinal diseases HSDN C2096293 Ent surgical result ear vertigo C1962963 Osteoporosis adverse event HSDN C0004134 Dyssynergia C1866398 Proteus-like syndrome (disorder) MalaCards C3146279 Coma C0008519 Ectopic tissue HSDN C4084788 Have dizziness C0000771 Abnormalities, drug induced HSDN C3898969 Have been vomiting C1333764 Gastric cronkhite canada polyposis MalaCards C0007758 Cerebellar ataxia C1866130 Rhombencephalosynapsis OrphaNet|MalaCards C4084784 Diarrhea C0017536 Giardiasis DiseaseOntology C2911645 Weight loss adverse event C1881600 Malignant vipoma MalaCards C3887638 Failure to thrive in infant C4014233 Immunodeficiency 22 MalaCards C0015672 Decreased energy C0009443 Common cold HSDN C0017565 Gingiva hemorrhage C1847197 Vascular malformation, primary intraosseous MalaCards C0030794 Pelvis pain C0302148 Blood clot HSDN C4085862 Bothered by nausea C0023343 Leprosy HSDN C2911645 Weight loss adverse event C0034494 Rabies (disorder) HSDN C0040485 Wryneck C0546878 Salaam spasms MalaCards C4084767 Bothered by vomiting C0812393 Cancer patients and suicide and depression HSDN C3829611 Nausea frequency C1962958 Hematoma adverse event HSDN C0013604 Edematous C0031538 Phimosis HSDN C0398650 Idiopathic thrombocytopenia purpura C0242584 Autoimmune thrombocytopenia MalaCards C0850758 Pain pelvic C0016542 Foreign body HSDN C4084788 Have dizziness C0031941 Pineal gland neoplasm HSDN C0000737 Abdomen pain C1336208 Stage iiia carcinoma of liver cells UMLS C0012833 Dizzy C0236969 Substance-related disorders HSDN C2984057 Have nausea C0003486 Aortic aneurysm HSDN C2237041 Shox gene with short stature C0265248 Ruvalcaba syndrome MalaCards C3815497 Cough C0022660 Kidney failure, acute HSDN C0018834 Brash C1970482 Potocki-lupski syndrome OrphaNet|HPO|MalaCards C0393759 Transient insomnia C1561841 Adjustment insomnia UMLS C1963091 Diarrhea adverse event C0042134 Uterine hemorrhage HSDN C1384666 Decreased hearing C3280011 Brittle cornea syndrome 2 MalaCards C0030552 Paralysis partial C0393576 Chorea acanthocytosis syndrome OrphaNet|MalaCards C4084724 Usual severity constipation C0220847 C hepatitis virus HSDN C3274924 Have been coughing C0036946 Sheep--diseases HSDN C0751295 Memory loss or impairment C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C3641755 Have constipation C0024115 Lung diseases HSDN C4085210 Usual severity pain C0022680 Polycystic kidney diseases HSDN C3539895 Pelvic pain occurs with bowel movement C0042065 Genitourinary neoplasms HSDN C0037036 Increased salivation C1868681 Dystonia 12 HPO C4084775 Usual severity weight loss C2984291 Glioblastoma multiforme pathway HSDN C1963091 Diarrhea adverse event C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C4084784 Diarrhea C2745948 Hyalinosis, systemic MalaCards C0030552 Paralysis partial C0266526 Norrie disease MalaCards|HPO C0151889 Reflexes tendon increased C2931291 Familial spastic paraparesis and deafness OrphaNet|MalaCards C0042963 Symptoms vomiting C0342859 Harderoporphyria HPO C4085317 Diarrhea frequency C0035439 Rheumatic heart disease HSDN C0030975 Disorders perception C0520998 Phosphene HSDN C0008031 Pain chest C1302282 Chromaffin cell neoplasm MalaCards C1963091 Diarrhea adverse event C0041316 Lymph node tuberculosis HSDN C0004134 Dyssynergia C3179455 Niemann-pick disease, type c1 MalaCards|HPO C2919142 Short stature adverse event C0265308 Baller-gerold syndrome OrphaNet|HPO|MalaCards C0022408 Disorder joint C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet C3539895 Pelvic pain occurs with bowel movement C0033046 Premenstrual syndrome HSDN C0023015 Language handicap C1970482 Potocki-lupski syndrome MalaCards C1384666 Decreased hearing C1856186 Deafness enamel hypoplasia nail defects MalaCards C4085317 Diarrhea frequency C0006147 Breast fed HSDN C0018681 Headache, cephalalgia C0033586 Failure, prosthesis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041316 Lymph node tuberculosis HSDN C0009676 Confusion state C0014038 Encephalitis HSDN C4084726 Distress cough C0030305 Pancreatitis HSDN C0042571 Vertigo subjective C0023092 Lassa fever OrphaNet|MalaCards C0002170 Alopecia disorders C0265201 De sanctis-cacchione syndrome MalaCards C0042755 Virilisation C0042932 Animal vocalizations HSDN C0026826 High muscle tone C1849678 Peroxisomal acyl-coa oxidase deficiency MalaCards|HPO C0010520 Skin cyanosis C1704212 Embolism embolus HSDN C0013362 Dysarthrias C0752353 Atrophy, muscular, spinobulbar OrphaNet|HPO C0270948 Neurogenic muscular atrophy C1834673 Facioscapulohumeral muscular dystrophy 1a MalaCards C4084768 Usual severity vomiting C0948039 Bacterial gastritis MalaCards C0013421 Dystonia C0000768 Congenital abnormality HSDN C0011175 Deficient fluid volume C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO C2911647 Weight gain adverse event C0011253 Delusions HSDN C0013404 Respiratory difficulty C1707407 Clear cell carcinoma of lung, large cell type UMLS C4085210 Usual severity pain C0019357 Keratitis, herpetic HSDN C0043094 Weight gain C1956257 Pulmonary stenosis HSDN C1145670 Failure respiratory C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0012147 Dientamoebiases DiseaseOntology C3641756 Have diarrhea C0854176 Malignant hepato-biliary neoplasm MalaCards C0557874 Global developmental delay C0409818 Chronic infantile neurological, cutaneous, and articular syndrome MalaCards|HPO C0860603 Anxiety symptom C2931246 Chromosome 17, trisomy 17p11 2 OrphaNet|HPO|MalaCards C0242936 Center pain C0033968 Psychotherapeutic technique HSDN C0037384 Snore C0001080 Achondroplasia HSDN C0242936 Center pain C0043395 Yellow fever HSDN C4084784 Diarrhea C0020192 Hyaline membrane disease HSDN C0426579 Anorexia symptom C1321581 Bezoar disorder HSDN C2984057 Have nausea C0038828 Arteriomesenteric duodenal ileus HSDN C0231528 Muscle pain generalized C0276742 Kerion celsi MalaCards C0518090 Frequency of pain question C3896673 Familial nonmedullary thyroid gland carcinoma MalaCards C0022346 Yellow skin C0278697 Childhood hepatoma, group ii UMLS C4084775 Usual severity weight loss C0221204 Lytic lesion HSDN C3203358 Alveolar hypoventilation C0006118 Brain neoplasms HSDN C0221263 Cafe au lait spot C0040411 Tongue neoplasms HSDN C0037384 Snore C1963235 Sick sinus syndrome adverse event HSDN C0030193 Sense of pain C0242184 Hypoxia UMLS C0035078 Failure kidney C2673883 Renal-hepatic-pancreatic dysplasia HPO C0020615 Hypoglycemia nos C0342728 3-methylglutaconic aciduria type 1 MalaCards|HPO C4084784 Diarrhea C0039483 Giant cell arteritis HSDN C0860603 Anxiety symptom C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C1963086 Confusion adverse event C0006114 Cerebral edema HSDN C0018784 Deafness sensorineural C1962962 Hyperpigmentation adverse event HSDN C4084784 Diarrhea C0018565 Acquired deformity of hand, nos HSDN C0575081 Abnormal gait C0878677 Glycogen storage disease type iib MalaCards C1549543 Administration method - pain C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0011991 Loose stools C0268124 Adenosine deaminase deficiency MalaCards C0018524 Hallucinate C0007095 Carcinoid tumor HSDN C1962972 Proteinuria adverse event C1962983 Cataract adverse event HSDN C0424755 Fever symptoms C0006274 Bronchiolitis, viral HSDN C0043352 Absent salivary secretion C0033770 Prune belly syndrome MalaCards|HPO C1963091 Diarrhea adverse event C1000587 Pemphigus HSDN C1557397 Adverse event associated with pain C0020564 Hypertrophy HSDN C4085211 Pain distress question C0015395 Burn eye HSDN C0002965 Crescendo angina C1963198 Pancreatitis adverse event HSDN C4085210 Usual severity pain C0015409 Eye injuries penetrating HSDN C0028738 Nystagmus C3805432 Cob1 MalaCards C0018772 Deafness C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0019209 Large liver C1720779 Apolipoprotein c-ii deficiency (disorder) HPO C0206160 Retic count elevated C0004576 Babesiosis HSDN C0043068 Friderichsen-waterhouse syndrome C0022667 Papillary necrosis HSDN C4084766 Vomiting C3146297 Study of behavior during childhood HSDN C0013421 Dystonia C0518450 Spinal fractures HSDN C0004604 Pain back C1859101 Chordoma of spinal column UMLS C4084768 Usual severity vomiting C3539923 Cdisc adas-cog - orientation summary score HSDN C0349588 Stature short C1857068 Ectodermal dysplasia and neurosensory deafness OrphaNet|MalaCards C0497406 Over weight C0035228 Respiratory hypersensitivity HSDN C0013404 Respiratory difficulty C0020615 Hypoglycemia HSDN C1145670 Failure respiratory C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal OrphaNet|HPO C0007166 Cardiac output decreased C0023903 Liver neoplasms HSDN C0036572 Convulsion C1963198 Pancreatitis adverse event HSDN C0518090 Frequency of pain question C0020619 Hypogonadism HSDN C0011168 Disorder deglutition C0015624 Fanconi syndrome HPO C0015672 Decreased energy C0018818 Ventricular septal defects HSDN C0149793 Transient monocular blindness C0039263 Takayasu arteritis MalaCards|HPO C0009792 Consciousness disorder C0020649 Hypotension HSDN C0242936 Center pain C0037313 Sleep HSDN C0027066 Myoclonic jerking C1847640 Kufor-rakeb syndrome MalaCards|HPO|UMLS C1962972 Proteinuria adverse event C0013504 Echinococcosis, hepatic HSDN C0019209 Large liver C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C0013528 Echo speech C1552527 Clinic / center - developmental disabilities HSDN C0028738 Nystagmus C1956391 Temporal arteritis MalaCards|HPO C3539889 Pelvic pain increasing in severity C0037929 Spinal cord injuries HSDN C0564822 Pain left leg C4047625 Pain co-occurrent and due to varicose veins of left leg UMLS C0009792 Consciousness disorder C0027651 Tumor HSDN C0085606 Urination urgency C1963674 Spinocerebellar ataxia 10 MalaCards|HPO C1962972 Proteinuria adverse event C0268382 Amyloid nephropathy MalaCards C1963091 Diarrhea adverse event C0403447 Chronic kidney insufficiency HSDN C0700078 Deep tendon reflex decrease C3150973 Thiamine metabolism dysfunction syndrome 4 (bilateral striatal degeneration and progressive polyneuropathy type) MalaCards|HPO C0035229 Respiratory function impaired C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C1963071 Back pain adverse event C0036421 Systemic scleroderma HSDN C1963086 Confusion adverse event C0030305 Pancreatitis HSDN C2029884 Hearing loss by exam C0011853 Diabetes mellitus, experimental HSDN C1963065 Apnea adverse event C3810212 Joubert syndrome 21 MalaCards C0043144 Wheeze C0264423 Asthma, occupational UMLS C2024878 Cardiovascular surgery result: dyspnea C0038356 Stomach neoplasms HSDN C2237041 Shox gene with short stature C4014479 Culler-jones syndrome MalaCards C0015468 Face pain C0005967 Bone neoplasms HSDN C3539895 Pelvic pain occurs with bowel movement C0010356 Cross infection HSDN C0542476 Forgetful C1096902 Infantile sialic acid storage disease MalaCards C0518090 Frequency of pain question C0011630 Dermatomycoses HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0011581 Depressive disorder HSDN C0857305 Thrombocytopenia purpura C1546533 Specimen source codes - abscess HSDN C3898969 Have been vomiting C1546949 Event consequence - death HSDN C0012833 Dizzy C0014852 Esophageal diseases HSDN C4084725 Usual severity cough C1956390 Cranial arteritis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0033075 Presbyopia HSDN C0878638 Tongue signs C0406727 Orofaciodigital syndrome 4 MalaCards C2911645 Weight loss adverse event C0007193 Cardiomyopathy, dilated HSDN C0036572 Convulsion C1848410 Xeroderma pigmentosum, variant type MalaCards C0013404 Respiratory difficulty C0854981 Stage iii large cell carcinoma of lung UMLS C0034933 Abnormal reflexes C0024408 Machado-joseph disease HSDN C0020538 Hbp C1578691 Congenital myxedema MalaCards C1963184 Nystagmus adverse event C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C0013421 Dystonia C0795623 Hepatitis a vaccine, inactivated HSDN C4085211 Pain distress question C0001429 Adenolymphoma HSDN C4084726 Distress cough C0034531 Experimental radiation injuries HSDN C3887638 Failure to thrive in infant C0520681 Central alveolar hypoventilation syndrome MalaCards C3815497 Cough C0036421 Systemic scleroderma OrphaNet|HSDN|MalaCards C4085317 Diarrhea frequency C0034494 Rabies (disorder) OrphaNet|HSDN|MalaCards C0026821 Cramp C2609414 Acute kidney injury HSDN C4085549 Dizziness C0030920 Peptic ulcer HSDN C0030552 Paralysis partial C0152054 Therapeutic touch HSDN C4084766 Vomiting C2963140 Arteriovenous fistula in use with two needles HSDN C4085210 Usual severity pain C1963088 Cystitis adverse event HSDN C0041834 Erythematous condition C0263637 Angioma serpiginosum, x-linked MalaCards C0234146 Absent reflex C1864171 Peroxisome biogenesis disorder, complementation group 12 MalaCards C0349588 Stature short C1850671 Myosclerosis, autosomal recessive HPO C4085862 Bothered by nausea C0043121 Wernicke encephalopathy HSDN C0033774 Skin pruritus C0021831 Intestinal diseases HSDN C2096293 Ent surgical result ear vertigo C0014474 Ependymoma HSDN C2203646 Jaundice C0001807 Aggressive behavior HSDN C0024031 Back pain lower back C0007787 Transient ischemic attack HSDN C1384666 Decreased hearing C2930971 Acroosteolysis dominant type OrphaNet|HPO|MalaCards C3539890 Pelvic pain causes awakening at night C3495422 Finding relating to sexuality and sexual activity HSDN C0917816 Deficiency mental C0796249 Mental retardation, x linked 47 HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0079173 Craniomandibular disorders HSDN C0002962 Angina C0020479 Hyperlipoproteinemia type iii HPO C0019825 Voice hoarseness C1962958 Hematoma adverse event HSDN C0020455 Hypergammaglobulinemia C0162812 Necrobioses HSDN C0005745 Blepharoptosis C0853240 Mobius ii syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0030790 Pelvis infection HSDN C2096293 Ent surgical result ear vertigo C1962986 Glaucoma adverse event HSDN C3815497 Cough C0030286 Pancreatic diseases HSDN C0151311 Cranial nerve palsy C1857352 Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy MalaCards C0018772 Deafness C1838416 Cleidocranial dysplasia, forme fruste, dental anomalies only HPO C0019559 Hip arthralgia C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards|UMLS C0851578 Disorder sleep C0220847 C hepatitis virus HSDN C1963170 Hypothermia adverse event C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C3146279 Coma C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0034150 Skin purpura C0043251 Wounds and injuries HSDN C0007758 Cerebellar ataxia C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0023885 Liver abscess C0854176 Malignant hepato-biliary neoplasm MalaCards C0013595 Eczematous dermatitis C2931817 Chromosome 2q37 deletion syndrome OrphaNet|HPO|MalaCards C0035078 Failure kidney C1846790 Joubert syndrome 4 (disorder) MalaCards|HPO C4085210 Usual severity pain C0085084 Motor neuron disease HSDN C0860603 Anxiety symptom C0002875 Cooley's anemia OrphaNet|HPO C1145670 Failure respiratory C0022739 Klippel-trenaunay-weber syndrome MalaCards C0018780 Frequencies hearing high loss C0751908 Vestibular neuronitis HSDN C0018772 Deafness C1849661 Acrootoocular syndrome MalaCards C0016199 Pain flank C0027672 Neoplastic syndromes, hereditary HSDN C1549543 Administration method - pain C1861172 Venous thromboembolism HSDN C0005745 Blepharoptosis C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C0020458 Hyperhydrosis C1275074 Odonto-onycho-dermal dysplasia MalaCards C0235153 Sensory hallucination C1112155 Hereditary non-polyposis colorectal cancer syndrome HPO C0037317 Sleep disturbance C3149705 Parkinson disease 1, autosomal dominant lewy body HPO C2107732 Consistent heat intolerance C3809006 Cardiofaciocutaneous syndrome 3 MalaCards C0917816 Deficiency mental C3280265 Mental retardation, autosomal recessive 18 MalaCards C0151786 Weakness muscle C0017185 Gastrointestinal neoplasms HSDN C0495461 Regurgitation and rumination of newborn C0554614 Other perinatal conditions UMLS C0013604 Edematous C0007785 Cerebral infarction HSDN C3887873 Hearing loss C0010034 Corneal diseases HSDN C0042798 Vision dim C1848533 Ataxia with vitamin e deficiency HPO C2984058 Have pain C0206368 Exfoliation syndrome HSDN C0426579 Anorexia symptom C4049994 Insulin resistance measurement HSDN C0036659 Sensation disorder C0919267 Ovarian neoplasm HSDN C0398650 Idiopathic thrombocytopenia purpura C0151744 Myocardial ischemia HSDN C0009421 Comatose C0041466 Typhoid fever MalaCards C4084775 Usual severity weight loss C0024788 Green monkey virus disease OrphaNet|MalaCards C0042798 Vision dim C0028866 Oculomotor nerve paralysis HSDN C1961131 Cough adverse event C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0085631 Abnormal excitement C1864851 Pigmented nodular adrenocortical disease, primary, 2 HPO|UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C0024305 Lymphoma, non-hodgkin HSDN C0007758 Cerebellar ataxia C1336537 Supratentorial meningioma MalaCards C0003811 Cardiac rhythm disturbance C0036391 Schwartz-jampel syndrome MalaCards|HPO C0518090 Frequency of pain question C3873472 Vulvovaginal gingival syndrome MalaCards C0026838 Spasticity muscle C3281200 Leukoencephalopathy, brain calcifications, and cysts UMLS C2919142 Short stature adverse event C0268425 Alstrom syndrome OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C1548578 Location characteristic id - smoking HSDN C2919142 Short stature adverse event C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0349588 Stature short C1857556 Hsd11b2, arg208his HPO C0036572 Convulsion C0009759 Conjunctival diseases HSDN C4084768 Usual severity vomiting C0262584 Carcinoma, small cell HSDN C3539896 Pelvic pain occurs with urination C0221752 Rbc urine HSDN C4084784 Diarrhea C0017689 Glucagonoma OrphaNet|MalaCards C1549543 Administration method - pain C0856761 Budd-chiari syndrome HSDN C0023015 Language handicap C0023529 Leukomalacia, periventricular HSDN C0398650 Idiopathic thrombocytopenia purpura C1962963 Osteoporosis adverse event HSDN C0032617 High urine output C0342257 Complications of diabetes mellitus HSDN C0231835 Respiration rate increased C0034345 Pyruvate dehydrogenase complex deficiency disease OrphaNet|MalaCards C4085210 Usual severity pain C0027430 Nasal polyps HSDN C0037316 Not enough sleeping C1456784 Paranoia HSDN C4084723 Constipation C0334533 Arteriovenous hemangioma HSDN C0557874 Global developmental delay C3279840 Methylmalonate semialdehyde dehydrogenase deficiency MalaCards C0020615 Hypoglycemia nos C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0520909 Ponv C0009940 Convalescence HSDN C0037763 Spasm C0041296 Tuberculosis HSDN C1384666 Decreased hearing C3281297 Deafness, autosomal dominant 4b MalaCards C0518090 Frequency of pain question C0949691 Spondylarthropathies HSDN C4084776 Weight loss C0013274 Patent ductus arteriosus HSDN C0038002 Spleen enlargement C3150343 Hemolytic anemia, nonspherocytic, due to hexokinase deficiency HPO C4084724 Usual severity constipation C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C2919142 Short stature adverse event C1859405 Bowen-conradi syndrome OrphaNet|HPO|MalaCards C0009792 Consciousness disorder C0004096 Asthma HSDN C1519353 Skin eruption papular C1866983 Scleroderma, familial progressive MalaCards C3898969 Have been vomiting C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3463815 Feel fatigue C0019294 Hernia, inguinal HSDN C4084766 Vomiting C0206083 Myelinoclasis, central pontine HSDN C3463815 Feel fatigue C0271737 Addison's disease due to autoimmunity OrphaNet C0015672 Decreased energy C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0151686 Growth retardation C0023374 Lesch-nyhan syndrome MalaCards C4084784 Diarrhea C0016509 Dermatoses, foot HSDN C2984058 Have pain C0028850 Ocular motility disorders HSDN C0015672 Decreased energy C0220847 C hepatitis virus HSDN C0727671 Red cross toothache drops C0040451 Resorption tooth HSDN C0020450 Hyperemesis gravidarum C1863959 Hyperthyroidism, familial gestational MalaCards|HPO C4084724 Usual severity constipation C0027947 Neutropenia HSDN C0019825 Voice hoarseness C0028064 Niemann-pick diseases MalaCards C0011991 Loose stools C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C2169806 Tic C1963064 Anxiety adverse event HSDN C4085211 Pain distress question C0025427 Mercury poisoning HSDN C0086437 Joint hypermobility C0432243 Spondyloepimetaphyseal dysplasia with joint laxity MalaCards|HPO|UMLS C0033774 Skin pruritus C0020579 Hypervitaminosis a HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0036864 Sexual relations HSDN C2315100 Pediatric failure to thrive C0220722 Cerebrooculofacioskeletal syndrome 1 HPO C1557397 Adverse event associated with pain C0015625 Fanconi anemia HSDN C4085642 Level of joint stiffness C2931370 Bilateral ulnar hypoplasia and mental retardation MalaCards C2024878 Cardiovascular surgery result: dyspnea C0007124 Noninfiltrating intraductal carcinoma HSDN C2237041 Shox gene with short stature C1853100 Cerebrooculofacioskeletal syndrome 4 MalaCards|HPO C0151908 Dry skin C1863006 Ameloonychohypohidrotic syndrome OrphaNet|MalaCards C0751295 Memory loss or impairment C1866983 Scleroderma, familial progressive MalaCards C0424755 Fever symptoms C1456865 Ureteral calculi HSDN C4085210 Usual severity pain C0014571 Epiphyses, slipped HSDN C4084784 Diarrhea C0011615 Dermatitis, atopic HSDN C4049644 Depression C1856493 Gaucher disease, norrbottnian type HPO C0424755 Fever symptoms C0011311 Dengue fever DiseaseOntology|OrphaNet|MalaCards C1963274 Vasculitis adverse event C0406645 Amyopathic dermatomyositis MalaCards C0023015 Language handicap C0000768 Congenital abnormality HSDN C2055366 Temporary loss of urinary control with sudden movement C0042025 Urinary stress incontinence UMLS C4084725 Usual severity cough C0040558 Toxoplasmosis HSDN C0003962 Ascites C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C0007815 Cerebrospinal fluid rhinorrhoea C0004935 Animal ethology HSDN C0036572 Convulsion C4048800 Telomeric 22q13 monosomy syndrome MalaCards C0013911 Emaciate C0035528 Riboflavin deficiency HSDN C0036572 Convulsion C0267372 Intestinal lymphatic obstruction MalaCards C0042928 Paralysis vocal cord C0011570 Mental depression HSDN C0023380 Lethargy C0342784 Pearson's marrow-pancreas syndrome HPO C4085210 Usual severity pain C0030804 Pemphigoid, benign mucous membrane HSDN C0015469 Facial paralysis C0796561 Melanoma vaccines HSDN C1963093 Dizziness adverse event C1548578 Location characteristic id - smoking HSDN C4085222 Nausea C0001173 Adult pyloric stenosis HSDN C0010038 Corneal opacity disorder C0035317 Retinal hemorrhage MalaCards C0162298 Stiffness joints C0796021 Lowry wood syndrome MalaCards C4084776 Weight loss C3150172 Mtdps8b MalaCards C0007859 Pain neck C0019625 Sinus histiocytosis HSDN C4084727 Cough frequency C0348018 Projections HSDN C2024878 Cardiovascular surgery result: dyspnea C1691228 Cystic kidney diseases HSDN C2984057 Have nausea C1962986 Glaucoma adverse event HSDN C0575081 Abnormal gait C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards C0162285 Edema eyelid C1850055 Peho syndrome OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0221026 X-linked agammaglobulinemia HPO C2032395 Pelvic pain on the left C0010356 Cross infection HSDN C2188194 Unreasonable fears of specific object, activity, situation C3495563 Unreasonable fear of enclosed places - elevators, tunnels UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0036879 Education sex HSDN C0010520 Skin cyanosis C0236969 Substance-related disorders HSDN C0012569 Double vision C0018802 Congestive heart failure HSDN C0007642 Cellulitis nos C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards C4084769 Vomiting frequency C2937225 Biotin deficiency disease MalaCards C0007758 Cerebellar ataxia C1850510 Sialidosis, type i OrphaNet|HPO C0242936 Center pain C0035585 Rickettsia infections HSDN C0020505 Excessive eating C0020538 Hypertensive disease HSDN C0853986 Lymphocytes decreased C2675526 Neutropenia, severe congenital, autosomal recessive 4 HPO C4085211 Pain distress question C0006430 Burning mouth syndrome HSDN C3539890 Pelvic pain causes awakening at night C0458219 Complex regional pain syndromes HSDN C3541349 Syncope C0038661 Suicide HSDN C0042928 Paralysis vocal cord C0750929 Arnold-chiari malformation, type i MalaCards C4085211 Pain distress question C0001080 Achondroplasia HSDN C1549543 Administration method - pain C0751922 Median neuropathy HSDN C0010200 Cough symptom C0037397 Behavior social HSDN C0233565 Bradykinesia C1853833 Parkinson disease 6, autosomal recessive early-onset HPO|UMLS C0023380 Lethargy C0011570 Mental depression HSDN C0151686 Growth retardation C1869118 Hypothyroidism, congenital, due to thyroid dysgenesis HPO C3887873 Hearing loss C0036202 Sarcoidosis HSDN C0010520 Skin cyanosis C0850803 Anaphylaxis (non medication) HSDN C4084766 Vomiting C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C1260922 Respiratory abnormality C0080040 Polio post syndrome DiseaseOntology|MalaCards C3641756 Have diarrhea C0035455 Rhinitis HSDN C4085210 Usual severity pain C0007789 Cerebral palsy HSDN C0009398 Color vision defects C0015408 Eye injury HSDN C1963281 Vomiting adverse event C1457883 Aggressive reaction HSDN C3898969 Have been vomiting C0023269 Leiomyosarcoma HSDN C0037383 Sneeze C0019270 Hernia HSDN C3539890 Pelvic pain causes awakening at night C0206630 Endometrial stromal sarcoma HSDN C2984058 Have pain C0029118 Opportunistic infections HSDN C0039231 Heartbeats increased C0268474 Hydroxykynureninuria MalaCards|HPO C4084769 Vomiting frequency C0031039 Effusion pericardial HSDN C0751401 Ophthalmoparesis C0393946 Myasthenic myopathy MalaCards C1961131 Cough adverse event C0019069 Hemophilia a HSDN C1963184 Nystagmus adverse event C1847024 Albinism, oculocutaneous, type ib (disorder) OrphaNet|HPO|MalaCards C0577560 Eye mass C0730120 Cysts of iris and ciliary body UMLS C3539892 Pelvic pain in front C0000768 Congenital abnormality HSDN C0013604 Edematous C0008519 Ectopic tissue HSDN C0011206 Delirium acute C0003838 Arterial occlusive diseases HSDN C0010520 Skin cyanosis C4050613 Anxiety scale (basc-2) HSDN C0221752 Rbc urine C1956390 Cranial arteritis MalaCards C0019572 Hairiness C0022758 Kap HSDN C4085211 Pain distress question C0085110 Severe combined immunodeficiency HSDN C0476250 Head neck mass C0272391 Remnants tonsil UMLS C0013604 Edematous C0027663 Neoplasms, multiple primary HSDN C1963086 Confusion adverse event C0270639 Lateral sinus thrombosis HSDN C3714772 Fever recurrent C1845076 Lymphoproliferative syndrome, x-linked, 2 MalaCards C0000737 Abdomen pain C2981236 Stage iii rectosigmoid cancer ajcc v6 UMLS C0013604 Edematous C0013514 Echinostomiasis HSDN C0030193 Sense of pain C0037942 Spinal osteophytosis HSDN C0557874 Global developmental delay C0752166 Bardet-biedl syndrome HPO C0013404 Respiratory difficulty C3163843 Chondrosarcoma of bone HSDN C0018784 Deafness sensorineural C1704212 Embolism embolus HSDN C0042798 Vision dim C3151138 Retinitis pigmentosa 39 (disorder) MalaCards|HPO C0030552 Paralysis partial C0221011 Malignant atrophic papulosis HSDN C0009421 Comatose C0717360 Disease lyme vaccine HSDN C0013604 Edematous C0039336 Gustatory sense HSDN C0027498 Nausea vomiting C0272129 Donath-landsteiner hemolytic anemia MalaCards C0018772 Deafness C0011882 Diabetic neuropathies HSDN C0042963 Symptoms vomiting C0085278 Antiphospholipid syndrome HSDN C1963093 Dizziness adverse event C0032285 Pneumonia HSDN C0851578 Disorder sleep C0559260 Congenital scoliosis HSDN C0020615 Hypoglycemia nos C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO C0036572 Convulsion C0011882 Diabetic neuropathies HSDN C0013378 Dysgensia C1005359 Pica pica bird HSDN C4084768 Usual severity vomiting C0019196 Hepatitis c DiseaseOntology|HSDN|MalaCards C0036572 Convulsion C0376524 Branchio-oculo-facial syndrome MalaCards|HPO C0036572 Convulsion C3536568 Epilepsy generalized idiopathic intractable UMLS C1549543 Administration method - pain C0036879 Education sex HSDN C0018784 Deafness sensorineural C1842465 Lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones OrphaNet|MalaCards C0015672 Decreased energy C0006663 Calcinosis HSDN C0022346 Yellow skin C3899981 Bclc stage a adult hepatocellular carcinoma UMLS C0036572 Convulsion C1266112 Diffuse melanocytosis UMLS C4084775 Usual severity weight loss C0920350 Autoimmune thyroiditis HSDN C0011991 Loose stools C0600564 Self-efficacy HSDN C0010200 Cough symptom C0016548 Foreign body migration HSDN C0018681 Headache, cephalalgia C3714644 Thymus neoplasms MalaCards C0850758 Pain pelvic C1956346 Coronary artery disease HSDN C0025323 Bleeding menstrual heavy C3179396 Glanzmann thrombasthenia, type a MalaCards C0042755 Virilisation C0021361 Female infertility HSDN C4084769 Vomiting frequency C0039841 Thiamine deficiency HSDN C1963281 Vomiting adverse event C0600104 Obsessive compulsive behavior HSDN C1549543 Administration method - pain C0025364 Mental status schedule HSDN C3887638 Failure to thrive in infant C3809877 Schaaf-yang syndrome MalaCards C4084784 Diarrhea C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0002962 Angina C1547044 Kind of quantity - smell HSDN C4085211 Pain distress question C0023869 Lithiasis HSDN C0042571 Vertigo subjective C0262584 Carcinoma, small cell HSDN C3665347 Vision impaired C3495801 Granulomatosis with polyangiitis MalaCards|HPO C3665386 Abnormal vision C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards|HPO C2911645 Weight loss adverse event C0027059 Myocarditis HSDN C0233514 Behavior abnormal C0751362 Narcolepsy-cataplexy syndrome MalaCards C4085211 Pain distress question C0019087 Hemorrhagic disorders HSDN C0151686 Growth retardation C1849157 Insulin-like growth factor i, resistance to OrphaNet C2984058 Have pain C0000786 Spontaneous abortion HSDN C2237041 Shox gene with short stature C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C0010200 Cough symptom C0030286 Pancreatic diseases HSDN C3641755 Have constipation C0265499 49,xxxxy chromosomal anomaly OrphaNet|MalaCards C0004604 Pain back C0032927 Precancerous conditions HSDN C2237041 Shox gene with short stature C0265232 Frontonasal dysplasia anomalad MalaCards C0020672 Body temperature decreased C0011881 Diabetic nephropathy HSDN C0015469 Facial paralysis C0038941 Incisional infection HSDN C0038506 Stutter C0033885 Psychoanalytic interpretation HSDN C0030552 Paralysis partial C0342442 Acth-dependent cushing's syndrome OrphaNet C0747556 Pharyngitis recurrent C2936917 Infantile polyarteritis MalaCards C4084723 Constipation C0031069 Familial mediterranean fever OrphaNet|HPO C1963077 Bone pain adverse event C1849435 Bicarbonate-wasting rta OrphaNet|HPO C0015402 Hemorrhage eye C0005604 Trauma birth HSDN C0424755 Fever symptoms C0425045 Sudden infant death HSDN C3665346 Loss sight C1836824 Amish infantile epilepsy syndrome HPO|UMLS C0013604 Edematous C0023891 Liver cirrhosis, alcoholic HSDN C4084775 Usual severity weight loss C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007098 Walker carcinoma 256 HSDN C0426579 Anorexia symptom C0001175 Acquired immunodeficiency syndrome HSDN C4085549 Dizziness C0039239 Sinus tachycardia HSDN C3665492 Pigmentations C2931390 Anophthalmia, cleft lip-palate, facial anomalies, and cns anomalies and hypothalamic disorder MalaCards C4084774 Have weight loss C1547044 Kind of quantity - smell HSDN C0030975 Disorders perception C0036349 Paranoid schizophrenia HSDN C2700617 Irritation - emotion C1862937 Ftdals1 HPO C3641755 Have constipation C0032914 Pre-eclampsia HSDN C3539890 Pelvic pain causes awakening at night C0022116 Ischemia HSDN C4085549 Dizziness C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards C0012833 Dizzy C2717757 Retinocochleocerebral vasculopathies MalaCards C1549543 Administration method - pain C0020540 Malignant hypertension HSDN C0013404 Respiratory difficulty C0340848 Pulmonary venoocclusive disease 2, autosomal recessive HPO|UMLS C0151786 Weakness muscle C1833372 Hypocalciuric hypercalcemia, familial, type iii MalaCards C0030193 Sense of pain C0026847 Spinal muscular atrophy HSDN C0018772 Deafness C0004364 Autoimmune diseases HSDN C0221166 Paraparesis C0746706 Myelitis necrotizing UMLS C4085211 Pain distress question C0022373 Disease, jejunal HSDN C0241137 Skin pallor C0242342 Sheehan syndrome OrphaNet|MalaCards C0030193 Sense of pain C1511207 Bladder urachal urothelial carcinoma UMLS C4085222 Nausea C0042384 Vasculitis HSDN C0233514 Behavior abnormal C2931840 Aspartylglucosamidase (aga) deficiency MalaCards C2188456 Urinary incontinence at least twice a week C0042024 Urinary incontinence UMLS C0521532 Diaphragmatic weakness C1306794 Wound botulism MalaCards C0030486 Extremity paralysis, lower C0021833 Intestinal fistula HSDN C0036572 Convulsion C0494475 Tonic - clonic seizures UMLS C0020796 Profoundly mentally retarded C3554316 Epileptic encephalopathy, early infantile, 15 MalaCards C4084774 Have weight loss C0025289 Meningitis HSDN C1384666 Decreased hearing C1854488 Spinocerebellar ataxia 13 MalaCards C1959630 Eye pain adverse event C0024449 Fungal mycetoma HSDN C2169806 Tic C0037650 Somatoform disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0042487 Venous thrombosis HSDN C0037763 Spasm C0038218 Status asthmaticus UMLS C2911645 Weight loss adverse event C0162534 Prion diseases HSDN C1069915 Vertigo C0086543 Cataract nos HSDN C0853986 Lymphocytes decreased C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C1963252 Tremor adverse event C1837218 Cleft palate, isolated HSDN C2032396 Pelvic pain on the right C0027095 Myosarcoma HSDN C0234132 Pyramidal sign C2931905 Olivopontocerebellar atrophy 3 MalaCards C0027497 Queasy C1457883 Aggressive reaction HSDN C4084802 Usual severity diarrhea C0037051 Behavior illness HSDN C0042963 Symptoms vomiting C0042214 Vaccinia HSDN C0034124 Pupillary disorder C0004096 Asthma HSDN C0242936 Center pain C0013240 Alveolar osteitis HSDN C4084784 Diarrhea C0086649 Mps iii c HPO C1963184 Nystagmus adverse event C0268228 Neuraminidase 1 deficiency HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0013395 Indigestion C1336858 Undifferentiated gastric carcinoma UMLS C3539893 Pelvic pain occurs with intercourse C0005491 Biofeedback HSDN C1963086 Confusion adverse event C0042594 Vestibular diseases HSDN C4085317 Diarrhea frequency C0001768 Agammaglobulinemia OrphaNet|MalaCards C4084768 Usual severity vomiting C1855652 Fetus small for gestational age HSDN C0013911 Emaciate C0031707 Phosphorus metabolism disorders HSDN C0009806 Constipate C0025269 Multiple endocrine neoplasia type 2b HSDN|HPO|UMLS C4084784 Diarrhea C0019195 Hepatitis, viral, human HSDN C1856661 Cornea cloudy C0268273 Gangliosidosis, generalized gm1, type 3 MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0024535 Malaria, falciparum HSDN C2199591 Earache of left ear C0810000 Other ear and sense organ disorders UMLS C2315100 Pediatric failure to thrive C0030312 Pancytopenia HSDN C3815497 Cough C0007784 Cerebral hemisphere hemorrhage HSDN C0018784 Deafness sensorineural C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome MalaCards C0424755 Fever symptoms C1546558 Specimen source codes - blister HSDN C4085661 Usual severity nausea C0020676 Hypothyroidism HSDN C1963087 Constipation adverse event C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0039070 Collapse fleeting C0015802 Femur fracture HSDN C0012569 Double vision C0039726 Disease, thalamic HSDN C0019572 Hairiness C1864872 Spondyloepimetaphyseal dysplasia, genevieve type MalaCards|HPO C0015469 Facial paralysis C0037939 Spinal neoplasms HSDN C2984058 Have pain C0085136 Central nervous system neoplasms HSDN C4084773 Bothered by weight gain C0702221 Tactual discrimination HSDN C0398650 Idiopathic thrombocytopenia purpura C1762616 Meningioma, benign, no icd-o subtype HSDN C0497406 Over weight C0085096 Peripheral vascular diseases HSDN C0009792 Consciousness disorder C0948163 Leukoaraiosis HSDN C0037384 Snore C0026640 Mouth neoplasms HSDN C0002962 Angina C0003860 Arteritis HSDN C3641755 Have constipation C0037274 Dermatologic disorders HSDN C0011991 Loose stools C0042162 Uveal neoplasms HSDN C3641756 Have diarrhea C0010346 Crohn disease MalaCards C0018772 Deafness C0021832 Intestinal diseases, parasitic HSDN C0020672 Body temperature decreased C1837371 Sudden infant death with dysgenesis of the testes syndrome OrphaNet|HPO|MalaCards C2984058 Have pain C0017510 Gestures HSDN C0948427 Bowel peristalsis decreased C0948779 Gastrointestinal hypomotility UMLS C0019209 Large liver C3553230 Congenital disorder of glycosylation, type iil MalaCards C4084767 Bothered by vomiting C0020541 Hypertension, portal HSDN C0005745 Blepharoptosis C2748801 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement HPO C4084788 Have dizziness C0812393 Cancer patients and suicide and depression HSDN C1963086 Confusion adverse event C0040053 Thrombosis HSDN C0018808 Murmur C0012628 Discrete subaortic stenosis HSDN C0002962 Angina C0038358 Gastric ulcer HSDN C3641756 Have diarrhea C0023364 Leptospirosis HSDN C1557397 Adverse event associated with pain C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C0037763 Spasm C0016052 Fibromuscular dysplasia HSDN C0007758 Cerebellar ataxia C0002895 Anemia, sickle cell HSDN C0349588 Stature short C0265344 Donohue syndrome OrphaNet|HPO C3274924 Have been coughing C0812393 Cancer patients and suicide and depression HSDN C4084802 Usual severity diarrhea C0001768 Agammaglobulinemia OrphaNet|MalaCards C4084723 Constipation C0019159 Hepatitis a HSDN C0009806 Constipate C0853697 Neutrophil count decreased HSDN C0002963 Angina variant C0003813 Arrhythmia sinus HSDN C0004134 Dyssynergia C0949595 Gonadal dysgenesis, 46,xx HPO C0007859 Pain neck C2586211 Thrombosis of blood vessel HSDN C3539889 Pelvic pain increasing in severity C0022410 Joint instability HSDN C0424755 Fever symptoms C0023470 Myeloid leukemia HSDN C0013404 Respiratory difficulty C0006840 Candidiasis HSDN C0026821 Cramp C0037199 Sinusitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0032310 Pneumonia, viral HSDN C0042024 Urine incontinence C0018923 Hemangiosarcoma HSDN C0013604 Edematous C0019209 Hepatomegaly HSDN C0037316 Not enough sleeping C0037369 Smoking HSDN C0019209 Large liver C0022739 Klippel-trenaunay-weber syndrome MalaCards C0019079 Bloody sputum C0011570 Mental depression HSDN C0008031 Pain chest C0042214 Vaccinia HSDN C0018775 Hearing loss bilateral C0019693 Hiv infections HSDN C1962972 Proteinuria adverse event C0023892 Biliary cirrhosis HSDN C0751093 Dystonia, limb C1843264 Dystonia 13, torsion OrphaNet|MalaCards C4084775 Usual severity weight loss C0018889 Helminthiasis HSDN C0002624 Amnesia retrograde C3539923 Cdisc adas-cog - orientation summary score HSDN C4084784 Diarrhea C0026640 Mouth neoplasms HSDN C3898969 Have been vomiting C3665596 Warts HSDN C0018772 Deafness C1838162 Mesomelia-synostoses syndrome MalaCards C4084767 Bothered by vomiting C0018188 Granuloma HSDN C0027497 Queasy C0036202 Sarcoidosis HSDN C1962972 Proteinuria adverse event C0034040 Puerperal disorders HSDN C0424755 Fever symptoms C0016398 Focal infection, dental HSDN C0007642 Cellulitis nos C0023240 Legionellosis MalaCards C4084774 Have weight loss C3542996 Mindfulness HSDN C1510417 Apraxia of gait C0036341 Schizophrenia HSDN C0474368 Childbirth pain C0428977 Bradycardia HSDN C1963087 Constipation adverse event C1527336 Sjogren's syndrome HSDN C4084784 Diarrhea C0037579 Soft tissue neoplasms HSDN C3641755 Have constipation C0004933 Behavior modification technique HSDN C2700617 Irritation - emotion C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0009421 Comatose C3163620 Hypotension adverse event HSDN C2024893 Cardiovascular surgery result: fatigue C0004623 Bacterial infections HSDN C1963249 Tinnitus adverse event C0752165 Angioma, venous, central nervous system HSDN C4084768 Usual severity vomiting C1333088 Colonic hamartomatous polyps MalaCards C0015469 Facial paralysis C1837355 Leukodystrophy, hypomyelinating, 2 MalaCards|HPO C2919142 Short stature adverse event C0406587 Wrinkly skin syndrome MalaCards|HPO C0007758 Cerebellar ataxia C4225383 Lichtenstein-knorr syndrome UMLS C0042420 Vasovagal episode C3827868 Tachycardia by ecg finding HSDN C0026826 High muscle tone C2984299 Asthma pathway HSDN C0018772 Deafness C0037937 Spine injury HSDN C3814874 Loss of appetite question C0019196 Hepatitis c DiseaseOntology|MalaCards C4084768 Usual severity vomiting C0028768 Obsessive-compulsive disorder HSDN C4084725 Usual severity cough C0016664 Fatigue fracture HSDN C0027497 Queasy C0029443 Osteomyelitis HSDN C1963249 Tinnitus adverse event C1336537 Supratentorial meningioma MalaCards C4084767 Bothered by vomiting C0342731 Deficiency of mevalonate kinase MalaCards C0018834 Brash C0810319 Other and unspecified gastrointestinal disorders UMLS C0015300 Ocular proptosis C2674574 Aortic aneurysm, familial thoracic 3 MalaCards C0030552 Paralysis partial C0033936 Psychoses, alcoholic HSDN C0557874 Global developmental delay C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0424755 Fever symptoms C1956258 Familial thrombotic thrombocytopenic purpura MalaCards|HPO C0009398 Color vision defects C1845407 Cone-rod dystrophy, x-linked, 3 HPO C0522224 Palsied C0023895 Liver diseases HSDN C0008031 Pain chest C0854891 Malignant pleural mesothelioma recurrent UMLS C2919142 Short stature adverse event C0265287 Acromicric dysplasia HPO C0034933 Abnormal reflexes C1550639 Specimen type - fistula HSDN C0003862 Pain joint C0852007 Scleroderma and associated disorders OrphaNet C0033377 Caudal displacement C0272066 Glycogen storage disease xii MalaCards|HPO C4085211 Pain distress question C0018571 Hand injury HSDN C0557874 Global developmental delay C0028064 Niemann-pick diseases MalaCards C2984058 Have pain C0026705 Mucopolysaccharidosis ii HSDN C0010200 Cough symptom C0302148 Blood clot HSDN C2132198 Abnormal blistering of the skin C0267372 Intestinal lymphatic obstruction MalaCards C0476273 Distress respiratory C1334680 Mediastinal seminoma UMLS C4084773 Bothered by weight gain C0002514 Amino acid metabolism, inborn errors HSDN C4085862 Bothered by nausea C0023676 Life style HSDN C0018772 Deafness C0026267 Mitral valve prolapse syndrome HSDN C0008031 Pain chest C0007273 Carotid artery diseases HSDN C0085632 Listlessness C1862937 Ftdals1 MalaCards|HPO|UMLS C1963071 Back pain adverse event C0344490 Sacral agenesis HPO C0009806 Constipate C0344315 Depressed mood HSDN C0012833 Dizzy C0010346 Crohn disease HSDN C0015799 Feminisation C3536727 Triploidy HSDN C1963252 Tremor adverse event C0010823 Cytomegalovirus infections HSDN C0002622 Amnesias C0796561 Melanoma vaccines HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0305062 Tetanus toxoids HSDN C4085549 Dizziness C0042018 Urinary calculi HSDN C2024893 Cardiovascular surgery result: fatigue C0020544 Renal hypertension HSDN C0028738 Nystagmus C0795947 Fryns-van den berghe syndrome MalaCards C1963087 Constipation adverse event C3463824 Myelodysplastic syndrome HSDN C4084726 Distress cough C0010481 Cushing syndrome HSDN C4085210 Usual severity pain C0004763 Barrett esophagus HSDN C0232461 Increased appetite C3554224 Leptin deficiency or dysfunction MalaCards C3898969 Have been vomiting C0026266 Mitral valve insufficiency HSDN C0002962 Angina C1547940 Specimen source codes - ulcer HSDN C0032617 High urine output C0004936 Mental disorders HSDN C0033774 Skin pruritus C0035457 Rhinitis, allergic, perennial HSDN C2984058 Have pain C0036974 Shock HSDN C0000737 Abdomen pain C0019112 Hemorrhoids HSDN C0002170 Alopecia disorders C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy HPO C4084769 Vomiting frequency C0017128 Fistula gastric HSDN C4084767 Bothered by vomiting C0039981 Thoracic neoplasms HSDN C4085548 Usual severity dizziness C0004933 Behavior modification technique HSDN C2911645 Weight loss adverse event C0221026 X-linked agammaglobulinemia HPO C2024878 Cardiovascular surgery result: dyspnea C0085090 Lymphoma, aids-related MalaCards C1961131 Cough adverse event C0036329 Schistosomiasis japonica DiseaseOntology C0242936 Center pain C0029124 Optic atrophy HSDN C0011991 Loose stools C0039128 Syphilis HSDN C0086437 Joint hypermobility C1845862 Creatine deficiency, x-linked MalaCards|HPO C0234428 Consciousness disturbance C0153122 Induced malaria MalaCards C2936821 Spinal cerebrospinal fluid leak C0520679 Sleep apnea, obstructive HSDN C2032395 Pelvic pain on the left C0005586 Bipolar disorder HSDN C2315100 Pediatric failure to thrive C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C0030193 Sense of pain C1762616 Meningioma, benign, no icd-o subtype HSDN C0042798 Vision dim C0265514 Dermatofibrosis lenticularis disseminata MalaCards|HPO C1962972 Proteinuria adverse event C0149721 Left ventricular hypertrophy HSDN C1549543 Administration method - pain C0030297 Pancreatic neoplasm HSDN C0349588 Stature short C2750066 Spondylo-megaepiphyseal-metaphyseal dysplasia MalaCards C0243026 Generalized infection C0268151 Classical galactosemia MalaCards|HPO C1963077 Bone pain adverse event C1833699 Osteopoikilosis, isolated MalaCards C0848203 Male pelvic pain C0030455 Parametritis HSDN C1549543 Administration method - pain C0023051 Laryngeal diseases HSDN C0424755 Fever symptoms C0008626 Congenital chromosomal disease HSDN C4084773 Bothered by weight gain C0042373 Vascular diseases HSDN C0031911 Pigment deposition C1836573 Griscelli syndrome, type 3 MalaCards C0036572 Convulsion C0032269 Pneumococcal infections HSDN C0015672 Decreased energy C0520799 Acute radiation syndrome HSDN C0013604 Edematous C0007140 Carcinosarcoma HSDN C0042963 Symptoms vomiting C0012691 Dislocations HSDN C4084768 Usual severity vomiting C0020517 Hypersensitivity HSDN C0497406 Over weight C0039980 Chest injury HSDN C4020887 Photodysphoria C0017083 Gangliosidoses MalaCards C1557397 Adverse event associated with pain C0014358 Enterocolitis, pseudomembranous HSDN C0086437 Joint hypermobility C0023931 Lobstein's disease HPO C0917816 Deficiency mental C0220687 Kbg syndrome MalaCards|HPO C0015676 Mental fatigue C0151744 Myocardial ischemia HSDN C3898969 Have been vomiting C0035235 Respiratory syncytial virus infections HSDN C0000737 Abdomen pain C0162624 Enoplida infection HSDN C0085636 Light sensitivity C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards|HPO|UMLS C1963063 Anorexia adverse event C0020538 Hypertensive disease HSDN C3539889 Pelvic pain increasing in severity C0034065 Pulmonary embolism HSDN C4084774 Have weight loss C0037397 Behavior social HSDN C0004604 Pain back C0005942 Bone diseases, endocrine HSDN C0018772 Deafness C1851879 Cleft lip with or without cleft palate, nonsyndromic, 8 HPO C0231528 Muscle pain generalized C0040558 Toxoplasmosis DiseaseOntology C0518090 Frequency of pain question C0032002 Pituitary diseases HSDN C0424755 Fever symptoms C0029401 Osteitis deformans HSDN C0574002 Foot swelling C0029443 Osteomyelitis UMLS C4042891 Sleep wake disorders C0040411 Tongue neoplasms HSDN C4084775 Usual severity weight loss C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0030554 Abnormal sensation C1962958 Hematoma adverse event HSDN C4084727 Cough frequency C0263662 Disseminated eosinophilic collagen disease HSDN C0042798 Vision dim C0544012 Aberfeld's syndrome MalaCards C1963063 Anorexia adverse event C4050613 Anxiety scale (basc-2) HSDN C0042024 Urine incontinence C0017178 Gastrointestinal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042024 Urinary incontinence HSDN C2165311 Delusion of missing a limb C0011253 Delusions UMLS C1962972 Proteinuria adverse event C0014859 Esophageal neoplasms HSDN C4084766 Vomiting C1304456 Congo hemorrhagic fever MalaCards C2242996 Tingling C1962986 Glaucoma adverse event HSDN C0035229 Respiratory function impaired C0270962 Multi-core congenital myopathy OrphaNet|MalaCards C0003862 Pain joint C0023788 Whipple disease OrphaNet|MalaCards C0518090 Frequency of pain question C0013117 Dreaming HSDN C0035078 Failure kidney C0268074 Indian childhood cirrhosis MalaCards C0007758 Cerebellar ataxia C0010674 Cystic fibrosis HSDN C2024893 Cardiovascular surgery result: fatigue C0272126 Evans syndrome OrphaNet|MalaCards C0476250 Head neck mass C0018671 Head and neck neoplasms UMLS C0085593 Chill C0017160 Gastroenteritis HSDN C0013404 Respiratory difficulty C0032066 Plague vaccines HSDN C0013404 Respiratory difficulty C0023473 Myeloid leukemia, chronic HSDN C0000727 Abdomen acute C1399870 Hydrocolpos HSDN C0004941 Behavioral symptoms C0035436 Rheumatic fever MalaCards C0012833 Dizzy C0014121 Bacterial endocarditis HSDN C0020673 Hypothermia (central) (local) C0020544 Renal hypertension HSDN C0018681 Headache, cephalalgia C0085129 Bronchial hyperreactivity HSDN C4084788 Have dizziness C0151744 Myocardial ischemia HSDN C3814530 Skin vesicle C1836284 Epidermolysis bullosa simplex with migratory circinate erythema OrphaNet|HPO C1549543 Administration method - pain C0019156 Hepatic veno-occlusive disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0206634 Liposarcoma, myxoid HSDN C0026825 Flaccidity muscle C1739094 Foodborne botulism MalaCards C0036572 Convulsion C1527366 Salaam seizures UMLS C0007758 Cerebellar ataxia C0751285 Maple syrup urine disease, thiamine responsive HPO C3641756 Have diarrhea C0029132 Disorder of the optic nerve HSDN C0522224 Palsied C0752090 Autoimmune disease models, nervous system HSDN C1963281 Vomiting adverse event C0027627 Neoplasm metastasis HSDN C1145670 Failure respiratory C2936502 Charge syndrome, familial MalaCards C4084788 Have dizziness C0020542 Pulmonary hypertension HSDN C3829611 Nausea frequency C0018817 Atrial septal defects HSDN C0027498 Nausea vomiting C0878675 Erdheim-chester disease MalaCards C2076646 Infraorbital eye pain left C1400948 Infraorbital; pain UMLS C0042571 Vertigo subjective C0003467 Anxiety HSDN C0036572 Convulsion C0270837 Automatism epileptic UMLS C0019825 Voice hoarseness C0013446 Acquired ear deformities HSDN C0008031 Pain chest C0003864 Arthritis HSDN C0040264 Ear ringing sound C0017638 Glioma HSDN C0018926 Emesis bloody C4049644 Depression HSDN C0018991 Paralysis one side of body C0016398 Focal infection, dental HSDN C2984057 Have nausea C0022104 Irritable bowel syndrome HSDN C4084788 Have dizziness C0033845 Pseudotumor cerebri HSDN C0000737 Abdomen pain C0038356 Stomach neoplasms HSDN C1069915 Vertigo C0042338 Herpesvirus 3, human HSDN C1963071 Back pain adverse event C0007138 Carcinoma, transitional cell HSDN C0030486 Extremity paralysis, lower C0036341 Schizophrenia HSDN C4085210 Usual severity pain C3160917 Bladder pain syndrome OrphaNet|MalaCards C4084767 Bothered by vomiting C0038587 Substance withdrawal syndrome HSDN C0040822 D tremors C0030297 Pancreatic neoplasm HSDN C4084788 Have dizziness C0079744 Diffuse large b-cell lymphoma HSDN C0009676 Confusion state C0005967 Bone neoplasms HSDN C0232950 Menstruation, vicarious C3647157 Other gynecologic disorders UMLS C2919142 Short stature adverse event C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C0018991 Paralysis one side of body C0375206 Hemiplegia and hemiparesis UMLS C0151786 Weakness muscle C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084767 Bothered by vomiting C0700095 Central neuroblastoma HSDN C0026838 Spasticity muscle C2930923 N-acetylneuraminic acid storage disease MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018621 Hay fever HSDN C0151786 Weakness muscle C0016169 Pathologic fistula HSDN C0036572 Convulsion C1832884 Hemiplegic migraine, familial type 1 MalaCards|HPO C0728710 Pupil constriction observed C0030271 Pancoast syndrome HSDN C0234376 Tremor action C4225223 Tremor, hereditary essential, 5 UMLS C0020455 Hypergammaglobulinemia C1535939 Pneumocystis jiroveci pneumonia HSDN C4085211 Pain distress question C0854912 Pineal germinoma HSDN C0040264 Ear ringing sound C1847319 Paraganglioma and gastric stromal sarcoma OrphaNet|HPO|MalaCards C0019209 Large liver C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0000727 Abdomen acute C0032966 Complication, neoplastic pregnancy HSDN C0030193 Sense of pain C0027030 Maggot infection HSDN C0013604 Edematous C0041324 Tuberculosis, osteoarticular HSDN C2203646 Jaundice C1861455 Stomatocytosis i HPO C1384666 Decreased hearing C0040997 Trigeminal neuralgia HSDN C0026205 Pupillary constriction C3812171 Bradycardia by ecg finding HSDN C1963252 Tremor adverse event C0014553 Absence epilepsy HSDN C0030193 Sense of pain C0038579 Substance abuse, intravenous HSDN C0020305 Fetal edema C0542241 Toxemia bacterial HSDN C0728710 Pupil constriction observed C0428977 Bradycardia HSDN C0426579 Anorexia symptom C0162637 Strongylida infections HSDN C0013421 Dystonia C0015745 Ingestive behavior HSDN C0030554 Abnormal sensation C1963274 Vasculitis adverse event HSDN C3815497 Cough C0042138 Uterine neoplasms HSDN C0034150 Skin purpura C0025289 Meningitis HSDN C0022346 Yellow skin C1096660 Ehlers-danlos syndrome type ix MalaCards C1963252 Tremor adverse event C0024530 Malaria HSDN C2712367 Other speech disturbances C0037822 Speech disorders UMLS C0701824 Gait staggering C0427164 High level sensorimotor gait UMLS C0015469 Facial paralysis C0677866 Brain stem neoplasms HSDN C1963093 Dizziness adverse event C0027902 Neuropsychological diagnosis HSDN C0030975 Disorders perception C0027765 Nervous system disorder HSDN C1279888 Proteinuria of undiagnosed cause C2931788 Atypical hemolytic uremic syndrome OrphaNet|MalaCards C3539891 Pelvic pain to the rear C0037369 Smoking HSDN C0476273 Distress respiratory C1855548 Laron syndrome type 2 HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0085084 Motor neuron disease HSDN C0349588 Stature short C2931093 Osteogenesis imperfecta, type 5 MalaCards C1963281 Vomiting adverse event C0027430 Nasal polyps HSDN C2984058 Have pain C0037275 Skin diseases, vesiculobullous HSDN C4084775 Usual severity weight loss C0266836 Infantile colic HSDN C0851578 Disorder sleep C0010054 Coronary arteriosclerosis HSDN C0030554 Abnormal sensation C0004935 Animal ethology HSDN C0332573 Macula C1335968 Vulvar intraepithelial neoplasia, differentiated type UMLS C3641755 Have constipation C0343376 B; paratyphoid fever DiseaseOntology|MalaCards C4085211 Pain distress question C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0030193 Sense of pain C0018789 Cardiac aneurysm HSDN C1260880 Nasal drip C1334643 Adenoid cystic carcinoma of maxillary sinus UMLS C2911645 Weight loss adverse event C0032131 Plasmacytoma HSDN C0007758 Cerebellar ataxia C0342728 3-methylglutaconic aciduria type 1 MalaCards C0007814 Cerebrospinal fluid otorrhea C0015464 Facial nerve diseases HSDN C1959630 Eye pain adverse event C0005758 Bulla HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0010383 Crowd HSDN C0010520 Skin cyanosis C0006281 Congenital bronchogenic cyst HSDN C0019209 Large liver C2931360 Weber klippel trenaunay MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0034088 Pulmonary valve insufficiency HSDN C0000727 Abdomen acute C0024530 Malaria HSDN C0018834 Brash C2750804 Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities MalaCards|HPO C0024031 Back pain lower back C0033923 Psychomotor function HSDN C3815497 Cough C0032227 Pleural effusion disorder HSDN C0000731 Abdomen distention C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO C0038990 Sweats C1302282 Chromaffin cell neoplasm MalaCards C0030193 Sense of pain C0006271 Bronchiolitis HSDN C2029884 Hearing loss by exam C0037199 Sinusitis HSDN C4084774 Have weight loss C0024620 Primary malignant neoplasm of liver MalaCards C1279888 Proteinuria of undiagnosed cause C0024117 Chronic obstructive airway disease HSDN C4084766 Vomiting C1704972 Genomic orientation HSDN C4085210 Usual severity pain C0024116 Lung diseases, fungal HSDN C0152169 Colic renal C0221752 Rbc urine HSDN C1963137 Hydrocephalus adverse event C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C0032285 Pneum C1863236 Scid due to ada deficiency, early-onset HPO C4084766 Vomiting C0022822 Hunchback formed after birth HSDN C0013604 Edematous C0013274 Patent ductus arteriosus HSDN C1963087 Constipation adverse event C0030521 Parathyroid neoplasms MalaCards C0015970 Fever unknown origin C0035358 Retroperitoneal neoplasm HSDN C0009763 Conjunctiva inflammation C1848411 Xeroderma pigmentosum, complementation group e HPO C0002962 Angina C0015732 Fecal incontinence HSDN C0700078 Deep tendon reflex decrease C1856186 Deafness enamel hypoplasia nail defects MalaCards C4049644 Depression C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0015970 Fever unknown origin C0024305 Lymphoma, non-hodgkin HSDN C0013404 Respiratory difficulty C0035435 Rheumatism HSDN C0030193 Sense of pain C1519486 Squamous cell breast carcinoma, large cell keratinizing variant UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C0520946 Emotional hypersensitivity HSDN C1384666 Decreased hearing C0016154 Fish disease HSDN C0162835 Hypopigmentation C0043346 Xeroderma pigmentosum MalaCards C1963281 Vomiting adverse event C1705714 Lats1 wt allele HSDN C1963091 Diarrhea adverse event C0033054 Prenatal exposure delayed effects HSDN C0004604 Pain back C0850803 Anaphylaxis (non medication) HSDN C1963087 Constipation adverse event C0079487 Helicobacter infections HSDN C0017565 Gingiva hemorrhage C3179396 Glanzmann thrombasthenia, type a MalaCards C4084768 Usual severity vomiting C1864996 Enteric neuropathy, familial MalaCards C0009676 Confusion state C0002726 Amyloidosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242231 Coronary stenosis HSDN C0030232 Color loss C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C0030552 Paralysis partial C0751895 Vasospasm, intracranial HSDN C4085210 Usual severity pain C0018572 Hand, foot and mouth disease HSDN C0019825 Voice hoarseness C1334670 Mediastinal mixed embryonal carcinoma and teratoma UMLS C0020672 Body temperature decreased C0036118 Salmonella infections, animal HSDN C3887638 Failure to thrive in infant C0268490 Tyrosinemia, type i MalaCards C0086565 Liver function abnormal C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0042963 Symptoms vomiting C2937421 Prostatic hyperplasia HSDN C0011991 Loose stools C0042781 Visceral myopathy MalaCards|UMLS C0026603 Motion sickness C0010709 Cyst HSDN C0037199 Sinus infection C3809641 Ciliary dyskinesia, primary, 25 MalaCards C0700590 Diaphoresis excessive C0040021 Thromboangiitis obliterans MalaCards C0518090 Frequency of pain question C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4085317 Diarrhea frequency C0016483 Food preferences HSDN C1963087 Constipation adverse event C0085258 Deficiency, yang HSDN C2029884 Hearing loss by exam C0032285 Pneumonia HSDN C1557397 Adverse event associated with pain C0041351 Tularemia HSDN C0015469 Facial paralysis C0024115 Lung diseases HSDN C0344315 Mood depressed C0268281 Infantile neuronal ceroid lipofuscinosis MalaCards|HPO C2025995 Cellulitis C2936881 Eosinophilic synovitis MalaCards C1963093 Dizziness adverse event C2984330 Chagas disease pathway HSDN C1963087 Constipation adverse event C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0349588 Stature short C1860145 Acrocraniofacial dysostosis OrphaNet|MalaCards C2984058 Have pain C0040517 Gilles de la tourette syndrome HSDN C1557397 Adverse event associated with pain C0018789 Cardiac aneurysm HSDN C4085211 Pain distress question C0007871 Uterine cervical incompetence HSDN C0042024 Urine incontinence C1849320 Sandhoff disease, adult type HPO C2029884 Hearing loss by exam C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0518090 Frequency of pain question C0007684 Central nervous system infection HSDN C4084802 Usual severity diarrhea C0027962 Melanocytic nevus HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0677866 Brain stem neoplasms HSDN C0085602 Polydypsia C0013336 Dwarfism HSDN C4084726 Distress cough C0041326 Pleural tuberculosis HSDN C0013404 Respiratory difficulty C0001580 Adolescent behavior HSDN C0424755 Fever symptoms C0035865 Disease rivers ross MalaCards C1963281 Vomiting adverse event C0022423 Judgement HSDN C4084767 Bothered by vomiting C0042812 Acuity visual HSDN C0424755 Fever symptoms C0005591 Avian disease HSDN C0037317 Sleep disturbance C0338503 Septo-optic dysplasia HPO C0030193 Sense of pain C0005745 Blepharoptosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0031049 Tuberculous pericarditis HSDN C0028961 Urine output decreased C0031036 Polyarteritis nodosa HSDN C0009806 Constipate C0795623 Hepatitis a vaccine, inactivated HSDN C4085211 Pain distress question C0206708 Cervical intraepithelial neoplasia HSDN C0085593 Chill C0854891 Malignant pleural mesothelioma recurrent UMLS C0036572 Convulsion C1845102 Hyperekplexia and epilepsy MalaCards|HPO C4085211 Pain distress question C1861172 Venous thromboembolism HSDN C3641755 Have constipation C0687150 Parathyroid gland adenocarcinoma MalaCards|HPO C0497247 Blood pressure elevation C0524620 Metabolic syndrome x MalaCards C2984058 Have pain C0020649 Hypotension HSDN C0013390 Cramps menstrual C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C4084725 Usual severity cough C0697038 Asclepias tuberosa HSDN C3146279 Coma C1865290 Hyperinsulinemic hypoglycemia, familial, 3 MalaCards C2237041 Shox gene with short stature C3887949 Apparent mineralocorticoid excess MalaCards C0013604 Edematous C0038160 Staphylococcal infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017128 Fistula gastric HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024266 Lymphocytic choriomeningitis DiseaseOntology|MalaCards C0004604 Pain back C0018674 Head trauma HSDN C0009193 Coccyxdynia C3662095 Chronic pain in coccyx for more than three months UMLS C0242936 Center pain C0005283 Beta thalassemia HSDN C0041657 Consciousness loss C0019163 Hepatitis b HSDN C1384666 Decreased hearing C0011581 Depressive disorder HSDN C3874954 Urinary urgency due to benign prostatic hypertrophy C0085606 Urgency of micturition UMLS C0013604 Edematous C0022593 Keratosis HSDN C0000737 Abdomen pain C0011581 Depressive disorder HSDN C3641755 Have constipation C0019829 Hodgkin disease HSDN C0241137 Skin pallor C0265265 Aase syndrome MalaCards|HPO C2911647 Weight gain adverse event C1963134 Hemorrhoids adverse event HSDN C4084727 Cough frequency C2073625 X-ray of chest: pleural effusion HSDN C3641756 Have diarrhea C0028796 Dermatitis, occupational HSDN C0042963 Symptoms vomiting C0002726 Amyloidosis HSDN C0017181 Gastrointestinal bleed C0268342 Ehlers-danlos syndrome type 6 HPO C0018777 Deafness, conductive C3266898 Waardenburg syndrome OrphaNet|MalaCards C0015230 Exanthem C0030331 Panniculitis, nodular migratory UMLS C4085210 Usual severity pain C0005686 Urinary bladder diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C0007786 Brain ischemia HSDN C0027497 Queasy C0019151 Hepatic encephalopathy HSDN C2024893 Cardiovascular surgery result: fatigue C0019337 Heroin dependence HSDN C3665347 Vision impaired C1854065 Late-onset retinal degeneration (disorder) HPO C1962972 Proteinuria adverse event C0036875 Disorders of sex development HSDN C3274924 Have been coughing C2981150 Uranostaphyloschisis HSDN C2219865 Anxiety with frequent urination or diarrhea C0003467 Anxiety UMLS C0026205 Pupillary constriction C0027092 Myopia HSDN C0011168 Disorder deglutition C0393551 Madras-type motor neurone disease MalaCards C0023530 Leukopenia C0342705 Folate malabsorption, hereditary MalaCards|HPO C4084802 Usual severity diarrhea C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0349588 Stature short C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C0030193 Sense of pain C2733623 Fibrosarcoma of bone UMLS C4085862 Bothered by nausea C0020255 Hydrocephalus HSDN C0019079 Bloody sputum C0029118 Opportunistic infections HSDN C1069915 Vertigo C0027832 Neurofibromatosis 2 OrphaNet|HPO C0013604 Edematous C0040558 Toxoplasmosis HSDN C0031911 Pigment deposition C0027656 Neoplasms, connective tissue MalaCards C0005745 Blepharoptosis C0342687 Dopamine beta hydroxylase deficiency HPO C4085548 Usual severity dizziness C0022758 Kap HSDN C0542476 Forgetful C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C1384666 Decreased hearing C1849661 Acrootoocular syndrome MalaCards C0917816 Deficiency mental C0022340 Late-infantile neuronal ceroid lipfuscinosis MalaCards C0042963 Symptoms vomiting C0033968 Psychotherapeutic technique HSDN C4085211 Pain distress question C0007684 Central nervous system infection HSDN C0005745 Blepharoptosis C0431406 Asymmetric crying face association OrphaNet|HPO C0151786 Weakness muscle C4225171 Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration UMLS C2984058 Have pain C0006413 Burkitt lymphoma HSDN C1963249 Tinnitus adverse event C0012691 Dislocations HSDN C1963137 Hydrocephalus adverse event C2677099 Crouzon syndrome with acanthosis nigricans (disorder) OrphaNet|HPO|MalaCards C0151740 Intracranial hypertension C0268155 Deficiency of galactokinase HPO C0497406 Over weight C0005940 Bone diseases HSDN C4084768 Usual severity vomiting C0265673 Congenital kyphosis HSDN C0150055 Pain chronic C0751406 Post-traumatic osteoporosis UMLS C0003910 Articulation disorder C0338451 Frontotemporal dementia HSDN C3815497 Cough C0014236 Endophthalmitis HSDN C0013404 Respiratory difficulty C0019069 Hemophilia a HSDN C0030552 Paralysis partial C0007134 Renal cell carcinoma HSDN C1963091 Diarrhea adverse event C0740340 Amyloidosis, familial HSDN C4042891 Sleep wake disorders C0518449 Control of hip fracture risk HSDN C0015672 Decreased energy C0021400 Influenza HSDN C0018784 Deafness sensorineural C0035412 Rhabdomyosarcoma HSDN C0012569 Double vision C0040034 Thrombocytopenia HSDN C0333240 Acute edema C0340105 Oxygen-induced pulmonary edema UMLS C4084776 Weight loss C0030499 Parasitic diseases HSDN C0018777 Deafness, conductive C1868390 Facioauriculoradial dysplasia OrphaNet|MalaCards C1963077 Bone pain adverse event C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C0030552 Paralysis partial C1859598 Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0024899 Mastocytosis HSDN C3539022 Pelvic pain decreasing in severity C1394494 Cystocele, unspecified HSDN C0031911 Pigment deposition C1706004 Anhydrotic ectodermal dysplasias MalaCards C3539020 Pelvic pain decreasing in frequency C0037313 Sleep HSDN C4084723 Constipation C0015802 Femur fracture HSDN C4084775 Usual severity weight loss C0042029 Urinary tract infection HSDN C1963063 Anorexia adverse event C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0002622 Amnesias C1999266 Depression adverse event HSDN C0035232 Diaphragmatic paralysis C0016196 Chest flail HSDN C4085222 Nausea C0002871 Anemia HSDN C0566625 Articulation, unintelligible C1838049 Epilepsy, nocturnal frontal lobe, type 1 MalaCards C0033774 Skin pruritus C0023055 Laryngeal neoplasm HSDN C0232466 Feeding difficulty C3808964 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 MalaCards C4084773 Bothered by weight gain C0014038 Encephalitis HSDN C2029884 Hearing loss by exam C0013261 Duane retraction syndrome HSDN C4085317 Diarrhea frequency C0043208 Wolman disease HPO C2919142 Short stature adverse event C3280598 Short-rib thoracic dysplasia 5 with or without polydactyly MalaCards C3898969 Have been vomiting C0005403 Bile reflux HSDN C2984058 Have pain C0032586 Polyradiculopathy HSDN C4085317 Diarrhea frequency C0013374 Dysgammaglobulinemia HSDN C0010200 Cough symptom C0001418 Adenocarcinoma HSDN C4084773 Bothered by weight gain C0520946 Emotional hypersensitivity HSDN C2237041 Shox gene with short stature C0268335 Ehlers-danlos syndrome type 1 HPO C0020615 Hypoglycemia nos C2931141 Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency MalaCards|HPO C0917816 Deficiency mental C1837206 Cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly HPO C0557874 Global developmental delay C1849811 Pili torti and developmental delay OrphaNet|MalaCards C0018772 Deafness C2745959 Spondyloepiphyseal dysplasia, congenita MalaCards|HPO C0018772 Deafness C0472813 X-linked agammaglobulinemia with growth hormone deficiency HPO C0034155 Thrombotic thrombocytopenic purpura C0314657 Genetic predisposition HSDN C0015672 Decreased energy C0349639 Juvenile myelomonocytic leukemia UMLS C0032617 High urine output C1704272 Benign prostatic hyperplasia HSDN C0033774 Skin pruritus C0019911 Hookworm infections HSDN C1963063 Anorexia adverse event C2609414 Acute kidney injury HSDN C0460137 Push down or depress C0393590 Fahr's syndrome (disorder) MalaCards|HPO C0518090 Frequency of pain question C0030353 Papilledema HSDN C0013404 Respiratory difficulty C0344434 Atrial fibrillation ecg HSDN C0413252 Hypothermia due to exposure C0043241 Wound infection HSDN C1557397 Adverse event associated with pain C0026764 Multiple myeloma HSDN C3274924 Have been coughing C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0015672 Decreased energy C1333039 Cll with igvh shm UMLS C0034151 Hyperglobulinemic purpura C0019209 Hepatomegaly HSDN C0020578 Hyperventilate C0242350 Erectile dysfunction HSDN C0497247 Blood pressure elevation C0025268 Multiple endocrine neoplasia type 2a OrphaNet|HPO C3665347 Vision impaired C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C0011991 Loose stools C0867389 Chronic graft-versus-host disease MalaCards C0034933 Abnormal reflexes C0004044 Asphyxia HSDN C0007859 Pain neck C0700251 Brachial plexus neuropathies HSDN C0522224 Palsied C0018939 Hematological disease HSDN C0242670 Chronic vegetative state C0238156 Hematoma, subdural, intracranial HSDN C2024893 Cardiovascular surgery result: fatigue C0005424 Biliary tract diseases HSDN C0015300 Ocular proptosis C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0240941 Scalp pruritus C1274146 Pruritic scalp dermatosis UMLS C0231218 Malaise generalized C1706732 Advanced adult hepatocellular carcinoma UMLS C3887873 Hearing loss C0024117 Chronic obstructive airway disease HSDN C2237041 Shox gene with short stature C0406584 Acrogeria, gottron type OrphaNet|HPO|MalaCards C0040034 Thrombocytopenia C0175691 Dubowitz syndrome MalaCards|HPO C0004134 Dyssynergia C0010823 Cytomegalovirus infections HSDN C0004604 Pain back C1853554 Radiation induced meningioma MalaCards C2024893 Cardiovascular surgery result: fatigue C0001418 Adenocarcinoma HSDN C0349588 Stature short C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome OrphaNet|MalaCards C0024032 Birth weight subnormal C1415737 Hsd11b2 gene HPO C4085222 Nausea C2137063 Ent surgical result - speech HSDN C1963180 Neck pain adverse event C1963067 Atrial fibrillation adverse event HSDN C4085317 Diarrhea frequency C1366535 Avp gene HSDN C0851578 Disorder sleep C0018818 Ventricular septal defects HSDN C0917816 Deficiency mental C0342196 Thyroid dyshormonogenesis 5 MalaCards|HPO C4085548 Usual severity dizziness C3244301 Coverage level - family HSDN C3146279 Coma C0268542 Ornithine carbamoyltransferase deficiency HPO C0013604 Edematous C0007350 Cat disease HSDN C3463815 Feel fatigue C0015423 Eyelid diseases HSDN C0413252 Hypothermia due to exposure C0042769 Virus diseases HSDN C1384666 Decreased hearing C1546847 Entity name part type - family HSDN C0007758 Cerebellar ataxia C0751785 Unverricht-lundborg syndrome OrphaNet|HSDN|HPO|MalaCards C0037771 Paraparesis spastic C0013393 Dysostoses HSDN C0036572 Convulsion C0280790 Adult anaplastic oligodendroglioma UMLS C0030486 Extremity paralysis, lower C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1959630 Eye pain adverse event C0035309 Retinal diseases HSDN C0019079 Bloody sputum C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0518090 Frequency of pain question C0004943 Behcet syndrome HSDN C0002622 Amnesias C0014553 Absence epilepsy HSDN C4085211 Pain distress question C0029883 Otitis media with effusion HSDN C1963281 Vomiting adverse event C0342873 Glutaric aciduria iii MalaCards|HPO C0700292 Arterial hypoxaemia C0019034 Hemoglobin sc disease MalaCards C3829611 Nausea frequency C1855652 Fetus small for gestational age HSDN C4085549 Dizziness C0035435 Rheumatism HSDN C3815497 Cough C0263662 Disseminated eosinophilic collagen disease HSDN C0030200 Intractable pain C0032787 Postoperative complications HSDN C0231218 Malaise generalized C2981628 Stage ivb intrahepatic cholangiocarcinoma UMLS C0239376 Lower extremity pain C0085096 Peripheral vascular diseases UMLS C1549543 Administration method - pain C0014065 Congenital cerebral hernia HSDN C4085317 Diarrhea frequency C0428478 Serum triglycerides raised HSDN C3463815 Feel fatigue C2931850 Aase smith syndrome 2 OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0024301 Lymphoma, follicular HSDN C0034155 Thrombotic thrombocytopenic purpura C0006118 Brain neoplasms HSDN C4084768 Usual severity vomiting C0005937 Bone cysts HSDN C0011991 Loose stools C0035333 Retinitis HSDN C0878638 Tongue signs C0268445 Normokalemic periodic paralysis MalaCards C3146279 Coma C0001418 Adenocarcinoma HSDN C0034150 Skin purpura C0019050 Hemoglobinuria, paroxysmal HSDN C0007758 Cerebellar ataxia C0034088 Pulmonary valve insufficiency HSDN C0006370 Bulimia C0036093 Salivary gland diseases HSDN C2984057 Have nausea C0040136 Thyroid neoplasm HSDN C4084767 Bothered by vomiting C1704436 Peripheral arterial diseases HSDN C0026821 Cramp C0003486 Aortic aneurysm HSDN C0003962 Ascites C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C1279888 Proteinuria of undiagnosed cause C0162316 Iron deficiency anemia HSDN C4084726 Distress cough C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C1963093 Dizziness adverse event C0007774 Cerebral arterial diseases HSDN C1961131 Cough adverse event C0238990 Acute lower respiratory tract infection MalaCards C1963063 Anorexia adverse event C0812393 Cancer patients and suicide and depression HSDN C0018524 Hallucinate C0030305 Pancreatitis HSDN C0043094 Weight gain C0013990 Pathological accumulation of air in tissues HSDN C0004134 Dyssynergia C0276496 Familial alzheimer disease (fad) MalaCards C0009792 Consciousness disorder C0019080 Hemorrhage HSDN C0270948 Neurogenic muscular atrophy C2931230 Vacuolar myopathy MalaCards C0424755 Fever symptoms C0010308 Congenital hypothyroidism HSDN C0030552 Paralysis partial C0042594 Vestibular diseases HSDN C0000727 Abdomen acute C0025160 Megacolon HSDN C0522224 Palsied C0017601 Glaucomas HSDN C0004134 Dyssynergia C0016542 Foreign body HSDN C0413252 Hypothermia due to exposure C0008065 Childhood behavior HSDN C0010200 Cough symptom C0018024 Goiter, retrosternal HSDN C0022346 Yellow skin C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C0038002 Spleen enlargement C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C0850758 Pain pelvic C0000768 Congenital abnormality HSDN C1963247 Ventricular tachycardia adverse event C1837839 Cardiomyopathy, dilated, 1o MalaCards|HPO C0019572 Hairiness C1261473 Sarcoma HSDN C4084774 Have weight loss C0027540 Necrosis HSDN C0234502 Agnosia visual C0809996 Blindness and vision defects UMLS C0004134 Dyssynergia C0037341 Slow virus diseases HSDN C0013604 Edematous C0006384 Bundle-branch block HSDN C0242936 Center pain C0162739 Hellp syndrome HSDN C0242936 Center pain C0000880 Acanthamoeba keratitis HSDN C0221263 Cafe au lait spot C0206730 Neurothekeoma HSDN C0013604 Edematous C0040213 Chondropathia tuberosa HSDN C0034933 Abnormal reflexes C0699828 Serotonergic syndrome HSDN C0003862 Pain joint C1963198 Pancreatitis adverse event HSDN C2911645 Weight loss adverse event C0752087 Myasthenia gravis, autoimmune, experimental HSDN C2024878 Cardiovascular surgery result: dyspnea C0037933 Spinal diseases HSDN C4084788 Have dizziness C1522133 High cholesterol level HSDN C3539892 Pelvic pain in front C0029400 Osteitis HSDN C0036572 Convulsion C0042109 Urticaria HSDN C0581323 Clavicle pain C0086181 Intravenous drug abuse UMLS C1963093 Dizziness adverse event C0453996 Tobacco smoking HSDN C0152169 Colic renal C0543541 Hyperglycinuria (disorder) MalaCards C2203646 Jaundice C0020522 Delayed hypersensitivity HSDN C4084768 Usual severity vomiting C0279606 Childhood hepatocellular carcinoma MalaCards C2242996 Tingling C0027868 Neuromuscular diseases HSDN C0018777 Deafness, conductive C2931889 Oral-facial-digital syndrome, type 2 MalaCards C1963281 Vomiting adverse event C0038013 Ankylosing spondylitis HSDN C0018834 Brash C0030920 Peptic ulcer HSDN C3463815 Feel fatigue C0013595 Eczema HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020120 Engineering humans HSDN C0242936 Center pain C0001396 Stokes-adams syndrome HSDN C0040822 D tremors C0020615 Hypoglycemia HSDN C0020505 Excessive eating C1962979 Burn adverse event HSDN C0007758 Cerebellar ataxia C1968550 Mental retardation, x-linked, syndromic 13 MalaCards|HPO C0041657 Consciousness loss C0012644 Animal disease models HSDN C2315100 Pediatric failure to thrive C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0007398 Catatonic C0276226 Herpes encephalitis HSDN C0018775 Hearing loss bilateral C0038356 Stomach neoplasms HSDN C2919142 Short stature adverse event C0220998 Hypothalamic hypothyroidism MalaCards C1549543 Administration method - pain C0175702 Williams syndrome HSDN C0018524 Hallucinate C0007440 Cathexis HSDN C0015938 Fetal macrosomia C0086468 Injuries, prenatal HSDN C0221263 Cafe au lait spot C0022822 Hunchback formed after birth HSDN C0010200 Cough symptom C1708045 Fetal lung adenocarcinoma UMLS C3665492 Pigmentations C0035305 Retinal detachment MalaCards C0007758 Cerebellar ataxia C3280766 Joubert syndrome 14 MalaCards C1384666 Decreased hearing C0406723 Growth retardation, alopecia, pseudoanodontia and optic atrophy MalaCards|HPO C0028738 Nystagmus C0398691 Hyperimmunoglobulinemia d MalaCards C0003862 Pain joint C2931883 Bilateral kienbock's disease MalaCards C2919142 Short stature adverse event C3887495 German syndrome OrphaNet|MalaCards C0085631 Abnormal excitement C0040188 Tic disorder HSDN C0028961 Urine output decreased C0687720 Central diabetes insipidus HSDN C0040822 D tremors C0162809 Kallmann syndrome MalaCards|HPO C0242936 Center pain C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0518090 Frequency of pain question C0032087 Plant poisoning HSDN C0035078 Failure kidney C2673609 Epidermolysis bullosa inversa dystrophica MalaCards C0007166 Cardiac output decreased C0040156 Thyrotoxicosis HSDN C4085210 Usual severity pain C0037072 Diseases sigmoid HSDN C0013404 Respiratory difficulty C3161104 Adult plch MalaCards C0497406 Over weight C1522133 High cholesterol level HSDN C1963063 Anorexia adverse event C2936779 Hydroxymethylbilane synthase deficiency MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0013743 Eisenmenger complex HSDN C3814874 Loss of appetite question C0026780 Mumps MalaCards C0007384 Cataplexy C1843366 Niemann-pick disease, type c2 MalaCards|HPO C0020673 Hypothermia (central) (local) C0043049 Water intoxication HSDN C0033774 Skin pruritus C0024138 Lupus erythematosus, discoid HSDN C4084767 Bothered by vomiting C1553188 Hemolysis - observation HSDN C0009806 Constipate C1333100 Colon epidermoid carcinoma UMLS C0015672 Decreased energy C0305062 Tetanus toxoids HSDN C0000737 Abdomen pain C0004943 Behcet syndrome OrphaNet|HSDN|HPO|MalaCards C0018524 Hallucinate C0751739 Basal ganglia cerebrovascular disease HSDN C1838869 Proximal neurogenic muscle weakness C0026205 Miosis disorder MalaCards C4085317 Diarrhea frequency C1970820 Fabry disease, cardiac variant HPO C0011206 Delirium acute C0034929 Reflex HSDN C2911647 Weight gain adverse event C1956346 Coronary artery disease HSDN C0018834 Brash C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C0007758 Cerebellar ataxia C2750220 Karak syndrome MalaCards C0269268 Breast hardness C0006145 Breast diseases UMLS C0917816 Deficiency mental C0085132 Mucopolysaccharidosis vii OrphaNet|HPO C4084784 Diarrhea C0595812 Fistula route HSDN C0231835 Respiration rate increased C1090821 Sepsis (invertebrate) HSDN C1279888 Proteinuria of undiagnosed cause C0010054 Coronary arteriosclerosis HSDN C0023380 Lethargy C0749098 Hematoma, subdural, acute HSDN C0151908 Dry skin C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C1549543 Administration method - pain C2607914 Allergic rhinitis (disorder) HSDN C0026838 Spasticity muscle C3151000 Hemorrhagic destruction of the brain, subependymal calcification, and cataracts MalaCards|HPO|UMLS C0332563 Papulae C0795944 Fountain syndrome MalaCards C0030552 Paralysis partial C0241158 Cicatrix skin HSDN C4084775 Usual severity weight loss C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C0012833 Dizzy C0002726 Amyloidosis HSDN C0012833 Dizzy C0035613 Rift valley fever OrphaNet|MalaCards C0242936 Center pain C0376545 Hematologic neoplasms HSDN C0002962 Angina C0041321 Tuberculosis, miliary HSDN C3829611 Nausea frequency C3539923 Cdisc adas-cog - orientation summary score HSDN C3665347 Vision impaired C0751254 Creutzfeldt-jakob disease, familial MalaCards|HPO C0030486 Extremity paralysis, lower C0022744 Knee injury HSDN C1963063 Anorexia adverse event C0740277 Bile duct carcinoma HPO C1963063 Anorexia adverse event C0004364 Autoimmune diseases HSDN C1557397 Adverse event associated with pain C0011848 Diabetes insipidus HSDN C0011991 Loose stools C0012561 Broad tapeworm infection DiseaseOntology|HSDN C4020887 Photodysphoria C1839564 Jensen syndrome MalaCards C0012569 Double vision C0003864 Arthritis HSDN C0015672 Decreased energy C0554114 Epstein-barr virus hepatitis MalaCards C0004134 Dyssynergia C3539916 Myoclonus, familial cortical MalaCards C0026838 Spasticity muscle C2931903 Menzel type olivopontocerebellar atrophy MalaCards C0019079 Bloody sputum C0024305 Lymphoma, non-hodgkin HSDN C0011991 Loose stools C0024117 Chronic obstructive airway disease HSDN C0026838 Spasticity muscle C0025202 Melanoma HSDN C0233514 Behavior abnormal C1843366 Niemann-pick disease, type c2 MalaCards C0018681 Headache, cephalalgia C0020604 Hypochondria HSDN C4084723 Constipation C0238027 Botulism, infantile OrphaNet|MalaCards C4084773 Bothered by weight gain C0031345 Pharyngeal diseases HSDN C0034155 Thrombotic thrombocytopenic purpura C0032797 Postpartum hemorrhage HSDN C0039070 Collapse fleeting C0036341 Schizophrenia HSDN C2984058 Have pain C0037928 Spinal cord diseases HSDN C0015300 Ocular proptosis C4014347 Pontocerebellar hypoplasia, type 10 MalaCards C1963065 Apnea adverse event C0008297 Choanal atresia HSDN C0020615 Hypoglycemia nos C0282577 Congenital disorders of glycosylation OrphaNet|MalaCards C0038506 Stutter C0600564 Self-efficacy HSDN C0020305 Fetal edema C0024299 Lymphoma HSDN C0017181 Gastrointestinal bleed C0079218 Fibromatosis, aggressive MalaCards|HPO C0231218 Malaise generalized C0279607 Adult primary hepatocellular carcinoma UMLS C1557397 Adverse event associated with pain C0600104 Obsessive compulsive behavior HSDN C3539895 Pelvic pain occurs with bowel movement C0037313 Sleep HSDN C2911645 Weight loss adverse event C0243013 Base learn problems HSDN C0006370 Bulimia C2350520 Olfactory perception HSDN C0016382 Cutaneous vascular engorgement C0085253 Adult-onset still disease OrphaNet|MalaCards C0242936 Center pain C0162557 Liver failure, acute HSDN C0233565 Bradykinesia C0392702 Abnormal involuntary movement UMLS C0036572 Convulsion C3553816 Spinocerebellar ataxia, autosomal recessive 13 MalaCards C0151889 Reflexes tendon increased C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C4084723 Constipation C1836704 Arrhythmogenic right ventricular dysplasia, familial, 7 MalaCards C0242936 Center pain C0013505 Cyst, pulmonary hydatid HSDN C4084725 Usual severity cough C0020615 Hypoglycemia HSDN C0009460 Communication impairment C0302826 Expressed emotion HSDN C0003079 Pupillary inequality C0027819 Neuroblastoma HSDN C2984057 Have nausea C0002940 Aneurysm HSDN C0026821 Cramp C0599412 Lordosis [mating posture] HSDN C0042024 Urine incontinence C0011586 Three dimensional vision HSDN C0151825 Ostalgia C0346072 Blue rubber bleb nevus syndrome OrphaNet|HPO|MalaCards C0023380 Lethargy C1859499 3-methylcrotonyl coa carboxylase 2 deficiency MalaCards|UMLS C4084788 Have dizziness C0029456 Osteoporosis HSDN C4084769 Vomiting frequency C3888013 Hypnoses HSDN C0917816 Deficiency mental C3554609 Mental retardation, autosomal recessive 35 MalaCards C3539889 Pelvic pain increasing in severity C0010695 Cystocele HSDN C4084775 Usual severity weight loss C0006107 Concussion HSDN C4085317 Diarrhea frequency C0358297 Anthrax vaccines HSDN C4084766 Vomiting C0376547 Aromatherapy HSDN C0241210 Speaking delay C1847501 Glut1 deficiency syndrome OrphaNet|MalaCards C0010200 Cough symptom C0155883 Chronic obstructive asthma MalaCards C0009676 Confusion state C0028768 Obsessive-compulsive disorder HSDN C0042798 Vision dim C0035334 Retinitis pigmentosa OrphaNet|MalaCards C0036396 Sciatica C0003090 Ankylosis HSDN C0009676 Confusion state C1832903 Migraine, sporadic hemiplegic HPO C0015469 Facial paralysis C0853240 Mobius ii syndrome OrphaNet|HPO|MalaCards C1963086 Confusion adverse event C0005967 Bone neoplasms HSDN C0851578 Disorder sleep C3151069 Chromosome 17p13.1 deletion syndrome MalaCards C0004134 Dyssynergia C0025517 Metabolic diseases HSDN C2919142 Short stature adverse event C1970482 Potocki-lupski syndrome MalaCards|HPO C2315100 Pediatric failure to thrive C0033770 Prune belly syndrome MalaCards|HPO C0007859 Pain neck C0178842 Sensory feedback HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024961 Injuries maxillofacial HSDN C3641756 Have diarrhea C0006277 Bronchitis HSDN C2203646 Jaundice C0024232 Lymphatic metastasis HSDN C0019559 Hip arthralgia C1836315 Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia MalaCards|UMLS C4085317 Diarrhea frequency C0497573 Condylomata acuminata in women HSDN C4084774 Have weight loss C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse MalaCards C0030486 Extremity paralysis, lower C0023903 Liver neoplasms HSDN C0034933 Abnormal reflexes C0037397 Behavior social HSDN C0011991 Loose stools C1835888 Diarrhea 4, malabsorptive, congenital MalaCards|HPO C0015672 Decreased energy C0151526 Premature birth HSDN C0518090 Frequency of pain question C0281865 Hip injury HSDN C0015469 Facial paralysis C0027429 Nasal obstruction present finding HSDN C4042891 Sleep wake disorders C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C1963086 Confusion adverse event C0007771 Intracranial arteriosclerosis HSDN C3898969 Have been vomiting C0268293 Corticosterone methyl oxidase type i deficiency HPO C0242936 Center pain C1532253 Sedentary lifestyle HSDN C1527344 Dysphonia C0036391 Schwartz-jampel syndrome MalaCards|HPO C1860844 Sparse, thin hair C1955934 Trichothiodystrophy syndromes MalaCards C0424755 Fever symptoms C0040250 Tinea capitis MalaCards C0041657 Consciousness loss C0748830 Skull fracture basilar HSDN C0042798 Vision dim C0007798 Cerebral ventricle neoplasm HSDN C1549543 Administration method - pain C0010635 Cystadenoma, mucinous HSDN C4084788 Have dizziness C0264903 Premature ventricular complex multifocal MalaCards C1145670 Failure respiratory C1261567 Congenital tracheal agenesis OrphaNet|MalaCards C0018784 Deafness sensorineural C0014544 Epilepsy HSDN C4084784 Diarrhea C0038013 Ankylosing spondylitis HSDN C3665347 Vision impaired C0282577 Congenital disorders of glycosylation MalaCards C0003962 Ascites C1865639 Gracile bone dysplasia MalaCards|HPO C0013404 Respiratory difficulty C0002940 Aneurysm HSDN C1963087 Constipation adverse event C0018790 Cardiac arrest HSDN C0178417 Anhedonia C0015328 Behavior, exploratory HSDN C0003962 Ascites C1142158 Hepatic vein occlusion MalaCards C2919142 Short stature adverse event C0085920 Brachial neuralgia MalaCards C0413252 Hypothermia due to exposure C0018818 Ventricular septal defects HSDN C0391860 Diffuse inflammations C0271417 Otitis externa, diffuse UMLS C1963252 Tremor adverse event C0031511 Pheochromocytoma MalaCards|HSDN C4084774 Have weight loss C0027412 Opioid-related disorders HSDN C4084776 Weight loss C0546323 Inferior vena cava membranous obstruction MalaCards C0018777 Deafness, conductive C0265253 Stickler syndrome (disorder) HPO C0038506 Stutter C0007785 Cerebral infarction HSDN C0030193 Sense of pain C0014177 Endosalpingosis UMLS C0013404 Respiratory difficulty C0022822 Hunchback formed after birth HSDN C0278152 Hemifacial spasms C0013238 Dry eye syndromes HSDN C4085317 Diarrhea frequency C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0003469 Anxiety disorder C0031485 Phenylketonurias MalaCards C0015672 Decreased energy C0011253 Delusions HSDN C4085211 Pain distress question C0003614 Appendiceal neoplasms HSDN C0241137 Skin pallor C0346303 Thyrotroph adenoma OrphaNet|MalaCards C4084769 Vomiting frequency C0010823 Cytomegalovirus infections HSDN C0013404 Respiratory difficulty C1456865 Ureteral calculi HSDN C0042963 Symptoms vomiting C0268525 5-oxoprolinase deficiency MalaCards|HPO|UMLS C4085549 Dizziness C1963235 Sick sinus syndrome adverse event HSDN C0086565 Liver function abnormal C0017920 Glycogen storage disease type i MalaCards|HPO C2237041 Shox gene with short stature C2931557 Chromosome 4 short arm deletion MalaCards C0155552 Hearing loss mixed C0016395 Focal dermal hypoplasia MalaCards|HPO C0030193 Sense of pain C0700359 Organophosphate poisoning HSDN C0518090 Frequency of pain question C0079774 Peripheral t-cell lymphoma HSDN C0003550 Broca aphasia C0751815 Carotid artery, internal, dissection HSDN C0027497 Queasy C3810814 Myocardial infarction ecg assessment HSDN C1557397 Adverse event associated with pain C0001828 Agricultural workers' diseases HSDN C2315100 Pediatric failure to thrive C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C0030554 Abnormal sensation C1261128 Progeria-like syndrome MalaCards C0022346 Yellow skin C0002875 Cooley's anemia OrphaNet|HPO C0028738 Nystagmus C1857588 Amaurosis hypertrichosis OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0015300 Exophthalmos HSDN C4085862 Bothered by nausea C0019195 Hepatitis, viral, human HSDN C0002962 Angina C0018817 Atrial septal defects HSDN C0040822 D tremors C0004352 Autistic disorder HSDN C0027497 Queasy C0030297 Pancreatic neoplasm HSDN C1549543 Administration method - pain C0039614 Tetanus HSDN C1384666 Decreased hearing C0027726 Nephrotic syndrome HSDN C2984057 Have nausea C0012979 Canine disease HSDN C0010200 Cough symptom C1263846 Attention deficit hyperactivity disorder HSDN C4084784 Diarrhea C1527429 Increased blood npn HSDN C0020673 Hypothermia (central) (local) C2004491 Cicatrix HSDN C0008031 Pain chest C0749226 Systolic ejection murmur aortic grade UMLS C3641756 Have diarrhea C0011303 Demyelinating diseases HSDN C1557397 Adverse event associated with pain C0033046 Premenstrual syndrome HSDN C2919142 Short stature adverse event C1832648 Hypoparathyroidism familial isolated OrphaNet|MalaCards C0042963 Symptoms vomiting C0033817 Pseudomonas infections HSDN C4084725 Usual severity cough C0085786 Hamman-rich syndrome MalaCards|HSDN C0009806 Constipate C0393911 Pure autonomic failure MalaCards C0015672 Decreased energy C0008625 Chromosome aberrations HSDN C0018772 Deafness C3501846 Noonan-like syndrome with loose anagen hair HPO C0012833 Dizzy C0029443 Osteomyelitis HSDN C3829611 Nausea frequency C0017601 Glaucomas HSDN C2032395 Pelvic pain on the left C0033578 Prostatic neoplasms HSDN C0497247 Blood pressure elevation C1412749 Bbs4 gene HPO C0015672 Decreased energy C0007453 Cattle disease HSDN C2315100 Pediatric failure to thrive C0037315 Sleep apnea syndromes HSDN C0018772 Deafness C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C0406407 Cholinergic pruritus C0162627 Skin diseases, bacterial UMLS C0034150 Skin purpura C0041321 Tuberculosis, miliary HSDN C2024878 Cardiovascular surgery result: dyspnea C0016085 Filariasis HSDN C0037384 Snore C1876185 Dysgnathia complex MalaCards C0015676 Mental fatigue C0033918 Military psychology HSDN C0184567 Pain acute C2936636 Anticipation, psychological HSDN C2984057 Have nausea C0007798 Cerebral ventricle neoplasm HSDN C0039070 Collapse fleeting C0020538 Hypertensive disease HSDN|UMLS C0018524 Hallucinate C2919115 Encounter due to bereavement HSDN C0018784 Deafness sensorineural C1832466 Capos syndrome OrphaNet|HPO C0004134 Dyssynergia C3554690 Ataxia-oculomotor apraxia 3 MalaCards|UMLS C2024878 Cardiovascular surgery result: dyspnea C0206629 Pulmonary blastoma OrphaNet|HSDN|MalaCards C0033377 Caudal displacement C0410203 X-linked centronuclear myopathy OrphaNet|HPO C4085211 Pain distress question C1956089 Osteophyte HSDN C0015230 Exanthem C0238198 Gastrointestinal stromal tumors MalaCards|HPO C0030794 Pelvis pain C0042029 Urinary tract infection HSDN C0033774 Skin pruritus C0034885 Rectal neoplasms HSDN C0018932 Bright red rectal bleeding C0282207 Cronkhite-canada syndrome MalaCards C2315100 Pediatric failure to thrive C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C0015672 Decreased energy C0003504 Aortic valve insufficiency HSDN C0027497 Queasy C0032285 Pneumonia HSDN C0001825 Agraphia C0376542 Cognitive science HSDN C0008031 Pain chest C0079487 Helicobacter infections HSDN C0020505 Excessive eating C0018467 Habituation, psychophysiologic HSDN C1963071 Back pain adverse event C0022658 Kidney diseases HSDN C2919142 Short stature adverse event C1854663 Chudley rozdilsky syndrome OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0010068 Coronary heart disease HSDN C3665386 Abnormal vision C1848640 Usher syndrome, type i, french variety, formerly HPO C0020538 Hbp C1867020 Scalp-ear-nipple syndrome OrphaNet|HPO|MalaCards C0022346 Yellow skin C2983709 Hepatocellular carcinoma by ajcc v6 stage UMLS C4085210 Usual severity pain C0027126 Myotonic dystrophy HSDN C0751495 Seizure focal C0014547 Epilepsies, partial UMLS C0010520 Skin cyanosis C0037018 Schwartzman reaction HSDN C0012833 Dizzy C3810814 Myocardial infarction ecg assessment HSDN C0020673 Hypothermia (central) (local) C0010823 Cytomegalovirus infections HSDN C0851578 Disorder sleep C0035066 Renal artery obstruction HSDN C0030552 Paralysis partial C0085648 Synovial cyst HSDN C0023530 Leukopenia C1720957 Hyper-igm immunodeficiency syndrome, type 3 MalaCards|HPO C0030193 Sense of pain C0031046 Pericarditis HSDN C4084776 Weight loss C1145670 Respiratory failure HSDN C0162298 Stiffness joints C0544012 Aberfeld's syndrome MalaCards C4085210 Usual severity pain C0497579 Genital herpes male HSDN C0030486 Extremity paralysis, lower C0017168 Gastroesophageal reflux disease HSDN C2919142 Short stature adverse event C0017925 Glycogen storage disease type vi OrphaNet|HPO|MalaCards C0015230 Exanthem C0744095 Food allergy to pork UMLS C0242936 Center pain C0020179 Huntington disease HSDN C0020505 Excessive eating C0037421 Social isolation HSDN C0497406 Over weight C0034929 Reflex HSDN C3463815 Feel fatigue C0039614 Tetanus HSDN C1963091 Diarrhea adverse event C0085859 Polyglandular type i autoimmune syndrome HPO C0007859 Pain neck C0006118 Brain neoplasms HSDN C3887638 Failure to thrive in infant C1843292 Skin fragility-woolly hair syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0016549 Foreign body reaction HSDN C4084766 Vomiting C0020621 Hypokalemia HSDN C1963137 Hydrocephalus adverse event C0796154 Simpson-golabi-behmel syndrome, type 1 MalaCards C0003862 Pain joint C3489856 Cold hypersensitivity MalaCards C0040822 D tremors C2698658 Orofaciodigital syndrome type 1 MalaCards C2096293 Ent surgical result ear vertigo C0037286 Skin neoplasms HSDN C0026838 Spasticity muscle C0405580 Adrenal cortical hypofunction HSDN C0005745 Blepharoptosis C0242387 Mandibulofacial dysostosis MalaCards|HPO C0007758 Cerebellar ataxia C0020255 Hydrocephalus HSDN C0019825 Voice hoarseness C1963106 Esophagitis adverse event HSDN C0476250 Head neck mass C0431555 Congenital pharyngeal polyp UMLS C0242936 Center pain C0026936 Mycoplasma infections HSDN C4085210 Usual severity pain C1527348 Brain hypoxia HSDN C0020305 Fetal edema C0152427 Polydactyly HSDN C1000483 Genus anemia C0342784 Pearson's marrow-pancreas syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C1610547 Production class code - pleasure HSDN C4084767 Bothered by vomiting C3280314 Combined malonic and methylmalonic aciduria MalaCards C2919142 Short stature adverse event C1260899 Anemia, diamond-blackfan MalaCards|HPO C0270948 Neurogenic muscular atrophy C0917713 Becker muscular dystrophy OrphaNet|HPO C4084726 Distress cough C0019372 Herpesviridae infections HSDN C1963071 Back pain adverse event C0009240 Cognition HSDN C0034150 Skin purpura C0018790 Cardiac arrest HSDN C3887873 Hearing loss C0039075 Syndactyly HSDN C0036572 Convulsion C1541317 Adult gliosarcoma UMLS C0012569 Double vision C0032586 Polyradiculopathy HSDN C3539022 Pelvic pain decreasing in severity C0009375 Colonic neoplasms HSDN C0037763 Spasm C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C3814530 Skin vesicle HSDN C4084766 Vomiting C0020732 Iatrogenic disease HSDN C2911647 Weight gain adverse event C0027746 Nerve degeneration HSDN C0424755 Fever symptoms C0024025 Louping ill DiseaseOntology|MalaCards C0004134 Dyssynergia C0022822 Hunchback formed after birth HSDN C0040822 D tremors C0009395 Color perception HSDN C0857305 Thrombocytopenia purpura C0011633 Dermatomyositis HSDN C2984058 Have pain C1704275 Pyomyositis HSDN C0000737 Abdomen pain C0036690 Septicemia HSDN C4084767 Bothered by vomiting C1552262 Nurse practitioner - family HSDN C0151786 Weakness muscle C0016542 Foreign body HSDN C0004604 Pain back C0423690 Facet joint pain UMLS C4084724 Usual severity constipation C0023890 Liver cirrhosis HSDN C1549543 Administration method - pain C0206693 Medullary carcinoma HSDN C0150055 Pain chronic C0001726 Affective symptoms HSDN C4084788 Have dizziness C0022423 Judgement HSDN C0015970 Fever unknown origin C0085409 Polyendocrinopathies, autoimmune HSDN C0030193 Sense of pain C0036920 Sezary syndrome HSDN C2237041 Shox gene with short stature C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C0033377 Caudal displacement C2931338 Chromosome 3, monosomy 3q13 MalaCards C0000737 Abdomen pain C0919691 Anastomotic leaks HSDN C3898969 Have been vomiting C1704436 Peripheral arterial diseases HSDN C0012833 Dizzy C0205788 Histiocytoid hemangioma HSDN C0018681 Headache, cephalalgia C0085138 Choroid plexus neoplasms HSDN|UMLS C0030486 Extremity paralysis, lower C0003615 Appendicitis HSDN C4084775 Usual severity weight loss C1962958 Hematoma adverse event HSDN C3539893 Pelvic pain occurs with intercourse C0019310 Hernia, obturator HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030567 Parkinson disease HSDN C0020538 Hbp C0342873 Glutaric aciduria iii MalaCards|HPO C0973461 Dysphasia C1832814 Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant MalaCards C0522224 Palsied C0205710 Alpers syndrome (disorder) MalaCards|HPO C0333422 Gumma C0276009 Gangosa UMLS C1962972 Proteinuria adverse event C1567743 Alport syndrome, autosomal dominant MalaCards|HPO C3898969 Have been vomiting C1855115 Methylmalonic aciduria, mut(0) type HPO C1963086 Confusion adverse event C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C0042024 Urine incontinence C0018188 Granuloma HSDN C0476250 Head neck mass C2937217 Cyst of nasal sinus UMLS C0030554 Abnormal sensation C2932716 Pseudohypoparathyroidism type 1c HPO C0178417 Anhedonia C0030567 Parkinson disease HSDN C3541349 Syncope C0967777 Mok protein, human HSDN C0011991 Loose stools C0162316 Iron deficiency anemia HSDN C3641756 Have diarrhea C0014175 Endometriosis HSDN C0231528 Muscle pain generalized C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C2984058 Have pain C0032046 Placenta previa HSDN C0242936 Center pain C0006114 Cerebral edema HSDN C0013456 Pain ear C0266589 Congenital ear anomaly nos (disorder) UMLS C1961131 Cough adverse event C0003486 Aortic aneurysm HSDN C2881444 Ocular pain, right eye C0497217 Other disease of eye UMLS C0030552 Paralysis partial C0270328 Diurnal enuresis HSDN C1963281 Vomiting adverse event C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0028738 Nystagmus C1837429 Pyruvate dehydrogenase phosphatase deficiency MalaCards|HPO C0587048 Upper extremity mass C0409786 Villonodular synovitis of distal radioulnar joint UMLS C4084766 Vomiting C0013926 Aeroembolism HSDN C0020580 Decreased sensation C0011849 Diabetes mellitus HSDN C0013404 Respiratory difficulty C0038358 Gastric ulcer HSDN C1557397 Adverse event associated with pain C0030489 Paraproteinemias HSDN C0012569 Double vision C1847843 Episodic ataxia, type 4 MalaCards C0030193 Sense of pain C0032816 Post-concussion headache HSDN C0013604 Edematous C0085136 Central nervous system neoplasms HSDN C4085211 Pain distress question C0022134 Islet cell adenoma HSDN C3539891 Pelvic pain to the rear C1458155 Mammary neoplasms HSDN C0086439 Activity decreased C1276035 Pena-shokeir syndrome type i OrphaNet|HPO|MalaCards C0022568 Inflammation corneal C0271270 Oculovestibuloauditory syndrome MalaCards C0727671 Red cross toothache drops C0012979 Canine disease HSDN C0752303 Manifestation, urological C0042029 Urinary tract infection HSDN C0851578 Disorder sleep C0022410 Joint instability HSDN C0038002 Spleen enlargement C0585216 Alpha-thalassemia myelodysplasia syndrome HPO C2984058 Have pain C0344423 Atrial flutter by ecg finding HSDN C2237041 Shox gene with short stature C1853136 Neutral lipid storage disease with myopathy MalaCards|HPO C4084768 Usual severity vomiting C0007099 Carcinoma in situ HSDN C0850758 Pain pelvic C0018199 Granuloma, plasma cell HSDN C0018784 Deafness sensorineural C0175699 Saethre-chotzen syndrome MalaCards|HPO C0242936 Center pain C0027149 Myxoma HSDN C3641756 Have diarrhea C0027947 Neutropenia HSDN C0030193 Sense of pain C0158328 Trigger finger HSDN C0349588 Stature short C1851878 Orofacial cleft 8 MalaCards|HPO C0018772 Deafness C1556682 Adverse event associated with infection HSDN C4084767 Bothered by vomiting C0036095 Salivary gland neoplasms HSDN C0030486 Extremity paralysis, lower C1690964 Cataract HSDN C0042963 Symptoms vomiting C0242383 Age related macular degeneration HSDN C0013604 Edematous C0037073 Sigmoid neoplasms HSDN C4084788 Have dizziness C1962983 Cataract adverse event HSDN C1963249 Tinnitus adverse event C1552052 Religious affiliation - meditation HSDN C0018991 Paralysis one side of body C0017178 Gastrointestinal diseases HSDN C4085222 Nausea C0524851 Neurodegenerative disorders HSDN C0030552 Paralysis partial C0001144 Acne vulgaris HSDN C4084767 Bothered by vomiting C0011875 Diabetic angiopathies HSDN C4085317 Diarrhea frequency C0021070 Immunoproliferative disease HSDN C3146279 Coma C1963198 Pancreatitis adverse event HSDN C4084767 Bothered by vomiting C0008350 Cholelithiasis HSDN C0033377 Caudal displacement C3492944 Lentiginosis profusa MalaCards C4084784 Diarrhea C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0043094 Weight gain C0028887 Oesophagostomiases HSDN C0917816 Deficiency mental C0432442 Chromosome 18p deletion syndrome OrphaNet|MalaCards C0042571 Vertigo subjective C3714644 Thymus neoplasms HSDN C4084775 Usual severity weight loss C0031090 Periodontal diseases HSDN C4084784 Diarrhea C0236733 Amphetamine-related disorders HSDN C0917816 Deficiency mental C1848200 Subcortical band heterotopia, x-linked HPO C0043094 Weight gain C0014170 Endometrial neoplasms HSDN C0018989 Paresis of one side of body C0270612 Leukoencephalopathies MalaCards C4084767 Bothered by vomiting C0015414 Eye neoplasms HSDN C4085211 Pain distress question C0376549 Roseolovirus infections HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0043397 Yellow fever, jungle MalaCards C0036572 Convulsion C0234534 Central convulsion UMLS C0812426 Kidney problem C0022680 Polycystic kidney diseases UMLS C2911645 Weight loss adverse event C0021345 Infectious mononucleosis HSDN C1279888 Proteinuria of undiagnosed cause C0005941 Bone diseases, developmental HSDN C0426579 Anorexia symptom C0860549 Refeed syndrome HSDN C0221232 Welts C0263343 Urticaria pigmentosa, multiple nodules or plaques UMLS C0005745 Blepharoptosis C3280240 Microcephaly, epilepsy, and diabetes syndrome MalaCards C4085211 Pain distress question C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C1000483 Genus anemia C0079136 Cockayne-touraine disease MalaCards C1549543 Administration method - pain C0085092 Parenting behavior HSDN C4084766 Vomiting C1868649 Panic disorder 1 HSDN C0024031 Back pain lower back C0085111 Ankle injury HSDN C1963065 Apnea adverse event C1842462 Campomelic dysplasia with autosomal sex reversal HPO C0000737 Abdomen pain C0026636 Mouth diseases HSDN C3641756 Have diarrhea C0042216 Poxvirus officinalis HSDN C1168240 Infusion site infiltration C1608954 Infusion site extravasation UMLS C0270948 Neurogenic muscular atrophy C2752074 Alpha-ketoglutarate dehydrogenase deficiency OrphaNet|HPO|MalaCards C4085211 Pain distress question C0038013 Ankylosing spondylitis DiseaseOntology|MalaCards C0426579 Anorexia symptom C0085682 Hypophosphatemia HSDN C0011206 Delirium acute C4050613 Anxiety scale (basc-2) HSDN C0042384 Vasculitis, nonspecific C0003490 Aortic arch syndrome MalaCards C4084775 Usual severity weight loss C0162425 Intent HSDN C0042963 Symptoms vomiting C0018273 Growth disorders HSDN C0018524 Hallucinate C0011269 Dementia, vascular HSDN C2919142 Short stature adverse event C1836602 Bruck syndrome 2 OrphaNet|HPO|MalaCards C0263629 Tumor-like lesions of the skin C0346004 Dilated pore of winer UMLS C2024893 Cardiovascular surgery result: fatigue C0042487 Venous thrombosis HSDN C2024893 Cardiovascular surgery result: fatigue C0003047 Animal disease HSDN C0231528 Muscle pain generalized C1853926 Nonaka myopathy MalaCards C0004604 Pain back C0005424 Biliary tract diseases HSDN C0037771 Paraparesis spastic C0037929 Spinal cord injuries HSDN C0034933 Abnormal reflexes C0003460 Anurias HSDN C0013404 Respiratory difficulty C0018193 Granuloma, foreign-body HSDN C0392702 Abnormal involuntary movement C4014621 Eiee25 MalaCards C0231528 Muscle pain generalized C0032285 Pneumonia UMLS C4084774 Have weight loss C0149514 Bronchitis acute HSDN C3463815 Feel fatigue C0085159 Seasonal affective disorder HSDN C0522224 Palsied C0031485 Phenylketonurias HSDN C2237041 Shox gene with short stature C2932716 Pseudohypoparathyroidism type 1c OrphaNet|HPO C0014591 Bleeding nose C0039445 Hereditary hemorrhagic telangiectasia OrphaNet|HPO|MalaCards C0151827 Pain eye C0043349 Xerophthalmia HSDN C0007758 Cerebellar ataxia C1850599 Leigh syndrome due to mitochondrial complex iv deficiency HPO C0015672 Decreased energy C1865290 Hyperinsulinemic hypoglycemia, familial, 3 MalaCards C0030975 Disorders perception C0036677 Sensory threshold HSDN C0018520 Breath odor C0030360 Papillon-lefevre disease HSDN C0030552 Paralysis partial C0700095 Central neuroblastoma HSDN C0032617 High urine output C0026103 Mikulicz disease HSDN C0037384 Snore C0018802 Congestive heart failure HSDN C4085210 Usual severity pain C0242172 Pelvic inflammatory disease HSDN C0020672 Body temperature decreased C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C1963135 Hepatic necrosis adverse event C0007095 Carcinoid tumor MalaCards C4084774 Have weight loss C0029132 Disorder of the optic nerve HSDN C4085211 Pain distress question C0018924 Hemarthrosis HSDN C0020538 Hbp C1863389 Apert-crouzon disease MalaCards C1549543 Administration method - pain C0015409 Eye injuries penetrating HSDN C0917816 Deficiency mental C1833538 Orofacial cleft 7 MalaCards C0349588 Stature short C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0497406 Over weight C1000483 Genus anemia HSDN C0349588 Stature short C3150675 Chromosome 15q24 duplication syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0042267 Vaginitis HSDN C4085210 Usual severity pain C0035920 Rubella HSDN C0151786 Weakness muscle C4085311 Depression - recess HSDN C0013362 Dysarthrias C3472711 Spinocerebellar ataxia 36 MalaCards C3887638 Failure to thrive in infant C0024523 Malabsorption syndrome MalaCards C1963087 Constipation adverse event C0024228 Lymphatic diseases HSDN C0024032 Birth weight subnormal C1856797 Estren-dameshek variant of fanconi pancytopenia HPO C0149793 Transient monocular blindness C0015029 Ethmoid sinusitis HSDN C1963071 Back pain adverse event C0032343 Poisoning HSDN C2187990 Unable to perform sex C1334698 Meningothelial cell neoplasm MalaCards C4084784 Diarrhea C0029295 Oropharyngeal neoplasms HSDN C0016199 Pain flank C1514839 Renal cell carcinoma associated with t(x;1)(p11.2;q21) UMLS C1963184 Nystagmus adverse event C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria MalaCards C0026858 Musculoskeletal pain C0683253 Psychological resilience HSDN C3887638 Failure to thrive in infant C0020625 Hyponatremia HSDN C0011570 Monopolar depression C3150344 Hyperhomocysteinemia, thrombotic, cbs-related HPO C1557397 Adverse event associated with pain C0014132 Endocrine gland neoplasms HSDN C4085222 Nausea C0011609 Drug eruptions HSDN C0013604 Edematous C0038379 Eye deviation HSDN C2024878 Cardiovascular surgery result: dyspnea C3163620 Hypotension adverse event HSDN C0027066 Myoclonic jerking C0752308 Hypoxia-ischemia, brain HSDN C0848203 Male pelvic pain C0085096 Peripheral vascular diseases HSDN C0011991 Loose stools C2706915 Language:-:point in time:^patient:- HSDN C0030552 Paralysis partial C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C0518090 Frequency of pain question C0038013 Ankylosing spondylitis DiseaseOntology|MalaCards C1263846 Attention deficit disorder with hyperactivity C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C4085661 Usual severity nausea C0020255 Hydrocephalus HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0524851 Neurodegenerative disorders HSDN C1145670 Failure respiratory C0220743 Childhood hypophosphatasia (disorder) MalaCards C0221170 Stiffness muscle C0751360 Becker generalized myotonia HPO|UMLS C4084766 Vomiting C0043065 Water electrolyte imbalance HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0038833 Superior vena cava syndrome HSDN C0040264 Ear ringing sound C0018799 Heart diseases HSDN C0030193 Sense of pain C0025295 Meningitis, pneumococcal HSDN C0242936 Center pain C0024904 Mastoiditis HSDN C0454644 Delayed language development C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO C0043068 Friderichsen-waterhouse syndrome C0038395 Streptococcal infections HSDN C4084775 Usual severity weight loss C0334463 Malignant fibrous histiocytoma MalaCards C0003962 Ascites C0867389 Chronic graft-versus-host disease MalaCards C0007398 Catatonic C0023418 Leukemia HSDN C2911645 Weight loss adverse event C0233629 Thinking and speaking disturbances HSDN C4084774 Have weight loss C0006663 Calcinosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0015457 Expression facial HSDN C3887873 Hearing loss C0220756 Niemann-pick disease, type c HSDN C1279888 Proteinuria of undiagnosed cause C0027962 Melanocytic nevus HSDN C1961131 Cough adverse event C0019829 Hodgkin disease OrphaNet C3887873 Hearing loss C0010340 Critical illness HSDN C4085211 Pain distress question C0040428 Abrasion dental HSDN C0751837 Gait ataxic C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO|UMLS C4084766 Vomiting C0279606 Childhood hepatocellular carcinoma MalaCards C2032396 Pelvic pain on the right C1548578 Location characteristic id - smoking HSDN C2984058 Have pain C3658267 Prostatic neoplasms, castration-resistant HSDN C0013604 Edematous C0032807 Postphlebitic syndrome HSDN C0700078 Deep tendon reflex decrease C1858280 Charcot-marie-tooth neuropathy, type 4b2, with early-onset glaucoma HPO C0240715 Perineal lump C0004767 Bartholin cyst UMLS C1557397 Adverse event associated with pain C0036039 Sadism HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1963266 Uveitis adverse event HSDN C0042963 Symptoms vomiting C0018213 Graves disease HSDN C0242936 Center pain C0002382 Alveolar bone loss HSDN C0013604 Edematous C1548483 Leishmaniasis vaccine HSDN C0018777 Deafness, conductive C0520946 Emotional hypersensitivity HSDN C0004134 Dyssynergia C1856491 Gaucher disease, type iiia HPO C2024893 Cardiovascular surgery result: fatigue C0039263 Takayasu arteritis OrphaNet|HPO|MalaCards C1963252 Tremor adverse event C0023055 Laryngeal neoplasm HSDN C0018991 Paralysis one side of body C0042510 Ventricular fibrillation HSDN C4084802 Usual severity diarrhea C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C1963184 Nystagmus adverse event C1855466 Hypomagnesemia 5, renal, with ocular involvement OrphaNet|HPO|MalaCards C0242936 Center pain C0014548 Epilepsy, generalized HSDN C3898969 Have been vomiting C0037933 Spinal diseases HSDN C0015970 Fever unknown origin C0043124 West nile fever HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0026769 Multiple sclerosis HSDN C0019209 Large liver C1837396 Congenital disorder of glycosylation, type ie MalaCards|HPO C4085642 Level of joint stiffness C0410189 Muscular dystrophy, emery-dreifuss OrphaNet|MalaCards C4042891 Sleep wake disorders C0032019 Pituitary neoplasms HSDN C0024031 Back pain lower back C1704436 Peripheral arterial diseases HSDN C4050613 Anxiety C1864112 Huntington disease-like 1 MalaCards|HPO C0232466 Feeding difficulty C3150172 Mtdps8b MalaCards|HPO C0015230 Exanthem C0263373 Keratosis spinulosus UMLS C0522224 Palsied C0852795 Increased insulin level HSDN C0000737 Abdomen pain C3899677 Childhood adrenal gland pheochromocytoma UMLS C0036572 Convulsion C0031345 Pharyngeal diseases HSDN C1549543 Administration method - pain C0276926 Schistosoma hematobium infection HSDN C4085210 Usual severity pain C0032463 Polycythemia vera HSDN C0595939 Stillborn C3278138 Fibrochondrogenesis 1 MalaCards C4084788 Have dizziness C0007134 Renal cell carcinoma HSDN C0812426 Kidney problem C0748311 Renal hypersensitivity UMLS C1279888 Proteinuria of undiagnosed cause C0595812 Fistula route HSDN C0036572 Convulsion C0752140 Intracranial embolism HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024116 Lung diseases, fungal HSDN C0042798 Vision dim C0039373 Tay-sachs disease OrphaNet C0518090 Frequency of pain question C2073625 X-ray of chest: pleural effusion HSDN C0013404 Respiratory difficulty C0033860 Psoriasis HSDN C4085222 Nausea C0014175 Endometriosis HSDN C0349588 Stature short C3179239 Osteopetrosis autosomal dominant type 2 OrphaNet|HPO|MalaCards C3146279 Coma C0175683 Citrullinemia HSDN|HPO C0030193 Sense of pain C0520459 Necrotizing enterocolitis HSDN C3887638 Failure to thrive in infant C3150215 Chromosome 6q24-q25 deletion syndrome MalaCards C0013604 Edematous C0004589 B. anthracis HSDN C0030552 Paralysis partial C0023441 Leukemia, experimental HSDN C0043094 Weight gain C0997768 Glaucoma HSDN C2984057 Have nausea C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C0020578 Hyperventilate C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO C4084767 Bothered by vomiting C0027819 Neuroblastoma HSDN C4084727 Cough frequency C0282607 Vascular neoplasms HSDN C0004134 Dyssynergia C3275471 Mental retardation, x-linked, syndromic, chudley-schwartz type MalaCards|UMLS C1963091 Diarrhea adverse event C0006264 Bronchial neoplasms HSDN C2203646 Jaundice C4049994 Insulin resistance measurement HSDN C4084774 Have weight loss C0162871 Aortic aneurysm, abdominal HSDN C3898969 Have been vomiting C1275081 Cardio-facio-cutaneous syndrome HPO C0042963 Symptoms vomiting C0003047 Animal disease HSDN C0030193 Sense of pain C0343200 Arteritis; giant cell, with polymyalgia rheumatica UMLS C0242936 Center pain C2267227 Bulimia nervosa HSDN C1963252 Tremor adverse event C0003838 Arterial occlusive diseases HSDN C0002962 Angina C0206138 Crest syndrome MalaCards C0010038 Corneal opacity disorder C3179194 Galns deficiency MalaCards C0042024 Urine incontinence C0042373 Vascular diseases HSDN C0349588 Stature short C1449844 Pseudohypoaldosteronism, type ii MalaCards C2315100 Pediatric failure to thrive C0019880 Homocystinuria HSDN C0042571 Vertigo subjective C0035309 Retinal diseases HSDN C0037763 Spasm C0022758 Kap HSDN C0022346 Yellow skin C0024198 Lyme disease HSDN C0085636 Light sensitivity C0162566 Porphyria cutanea tarda HSDN C0557874 Global developmental delay C1836861 Fanconi anemia, complementation group i MalaCards C0497247 Blood pressure elevation C1970827 Phosphoribosylpyrophosphate synthetase superactivity MalaCards C4085317 Diarrhea frequency C0242339 Dyslipidemias HSDN C2911645 Weight loss adverse event C3827868 Tachycardia by ecg finding HSDN C0917816 Deficiency mental C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards|HPO C1145670 Failure respiratory C3711162 Metatropic dysplasia type 1 MalaCards C0857305 Thrombocytopenia purpura C1963137 Hydrocephalus adverse event HSDN C2032395 Pelvic pain on the left C2706915 Language:-:point in time:^patient:- HSDN C0018784 Deafness sensorineural C1563720 Kallmann syndrome 2 (disorder) MalaCards|HPO C0750426 Wbc elevated C1801959 Histiocytic medullary reticulosis (disorder) MalaCards C0042755 Virilisation C2936421 Sex chromosome disorders of sex development HSDN C1279888 Proteinuria of undiagnosed cause C0021843 Intestinal obstruction HSDN C0009792 Consciousness disorder C0428953 Ecg infarction myocardial HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029412 Hypertrophic pulmonary osteoarthropathy HSDN C0917816 Deficiency mental C1853566 Genitopatellar syndrome OrphaNet|HPO|MalaCards C1963252 Tremor adverse event C1963198 Pancreatitis adverse event HSDN C0018784 Deafness sensorineural C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C1279888 Proteinuria of undiagnosed cause C0027439 Nasopharyngeal neoplasms HSDN C4085548 Usual severity dizziness C0036974 Shock HSDN C4084784 Diarrhea C0006114 Cerebral edema HSDN C3898969 Have been vomiting C0007133 Carcinoma, papillary HSDN C3829611 Nausea frequency C0041466 Typhoid fever HSDN C0043094 Weight gain C0600260 Lung diseases, obstructive HSDN C0036572 Convulsion C0032249 Plummer vinson syndrome MalaCards C2029884 Hearing loss by exam C0019829 Hodgkin disease HSDN C0007758 Cerebellar ataxia C0039538 Teratoma HSDN C0036572 Convulsion C0751524 Simple partial status epilepticus UMLS C4020887 Photodysphoria C1847132 Albinism, oculocutaneous, type i, temperature-sensitive MalaCards|HPO C0011991 Loose stools C0947622 Cholecystolithiasis HSDN C1557397 Adverse event associated with pain C0013922 Embolism HSDN C0018991 Paralysis one side of body C0022661 Kidney failure, chronic HSDN C0015230 Exanthem C0152063 Streptobacillus moniliformis infection DiseaseOntology|MalaCards C0015672 Decreased energy C0086774 Cold hemoglobinuria MalaCards C0030193 Sense of pain C0006261 Bronchial diseases HSDN C1971624 Appetite absent C0235387 Porphyria type syndrome OrphaNet C0013604 Edematous C0027439 Nasopharyngeal neoplasms HSDN C0018681 Headache, cephalalgia C0280623 Cns tumor, childhood choroid plexus UMLS C0012833 Dizzy C0005935 Bone conduction HSDN C1527344 Dysphonia C0080107 Fistula, respiratory tract HSDN C2032395 Pelvic pain on the left C0011854 Diabetes mellitus, insulin-dependent HSDN C4084767 Bothered by vomiting C0220654 Meningeal carcinomatosis HSDN C0030193 Sense of pain C0033324 Prognathism HSDN C0575081 Abnormal gait C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C1963281 Vomiting adverse event C0027643 Neoplasm recurrence, local HSDN C0522224 Palsied C0020459 Hyperinsulinism HSDN C1527344 Dysphonia C3554605 Mc3dn2 MalaCards C0019209 Large liver C2919796 Glycogen storage disease type ia MalaCards C0034150 Skin purpura C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0522224 Palsied C0027126 Myotonic dystrophy HSDN C0013421 Dystonia C0016399 Seizure focal motor HSDN C1963281 Vomiting adverse event C2981150 Uranostaphyloschisis HSDN C0035229 Respiratory function impaired C0041341 Tuberous sclerosis HPO C0086439 Activity decreased C0000744 Abetalipoproteinemia HSDN C0007758 Cerebellar ataxia C1853116 Spinocerebellar ataxia, autosomal recessive 8 (disorder) OrphaNet|UMLS|HPO|MalaCards C0027498 Nausea vomiting C0014859 Esophageal neoplasms MalaCards C2984058 Have pain C0021125 Impulsive behavior HSDN C4084767 Bothered by vomiting C0004659 Bacteriuria HSDN C0019825 Voice hoarseness C0027441 Nasopharyngitis HSDN C0162298 Stiffness joints C0877752 Stiffness of joint, nec, involving pelvic region and thigh in mdr19_0 UMLS C4084723 Constipation C2748910 Rett syndrome, atypical MalaCards|HPO C2029884 Hearing loss by exam C0020473 Hyperlipidemia HSDN C4049644 Depression C0393590 Fahr's syndrome (disorder) MalaCards|HPO C0030554 Abnormal sensation C0001807 Aggressive behavior HSDN C0006271 Inflammation of the bronchioles C3889474 Bardet-biedl syndrome 16 MalaCards C1000483 Genus anemia C0271994 Hereditary persistence of fetal hemoglobin thalassemia MalaCards C1557397 Adverse event associated with pain C0033289 Family relationship, professional HSDN C0413252 Hypothermia due to exposure C0020488 Hypernatremia HSDN C0917816 Deficiency mental C0268632 Homocarnosinosis OrphaNet|MalaCards C1963071 Back pain adverse event C0011168 Deglutition disorders HSDN C0018524 Hallucinate C0030499 Parasitic diseases HSDN C0015672 Decreased energy C0011881 Diabetic nephropathy HSDN C4084774 Have weight loss C0005686 Urinary bladder diseases HSDN C0015230 Exanthem C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C1557397 Adverse event associated with pain C0024138 Lupus erythematosus, discoid HSDN C3815497 Cough C0040053 Thrombosis HSDN C4084766 Vomiting C0021361 Female infertility HSDN C1319541 On examination - right eye proliferative diabetic retinopathy C0011849 Diabetes mellitus UMLS C0030552 Paralysis partial C0003467 Anxiety HSDN C0036572 Convulsion C0020488 Hypernatremia UMLS C0024031 Back pain lower back C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C1262148 Decreased grip strength C1850808 Miyoshi myopathy MalaCards|UMLS C4084725 Usual severity cough C0026771 Trauma multiple HSDN C4084775 Usual severity weight loss C0027658 Neoplasms, germ cell and embryonal HSDN C0018681 Headache, cephalalgia C1334184 Grade iv infratentorial astrocytic neoplasm UMLS C4084769 Vomiting frequency C0027625 Circulating neoplastic cells HSDN C2024878 Cardiovascular surgery result: dyspnea C0036690 Septicemia HSDN C1557397 Adverse event associated with pain C0007129 Merkel cell carcinoma MalaCards|HSDN C2242996 Tingling C0013990 Pathological accumulation of air in tissues HSDN C0020578 Hyperventilate C0220754 Biotinidase deficiency MalaCards|HPO C1557397 Adverse event associated with pain C0036349 Paranoid schizophrenia HSDN C0162298 Stiffness joints C2745948 Hyalinosis, systemic MalaCards C0000737 Abdomen pain C0007194 Hypertrophic cardiomyopathy HSDN C2237041 Shox gene with short stature C0265226 Hecht syndrome (disorder) OrphaNet|HPO C1527344 Dysphonia C0011633 Dermatomyositis MalaCards C0476273 Distress respiratory C0238461 Anaplastic thyroid carcinoma OrphaNet C3539023 Pelvic pain increasing in frequency C0033873 Psychiatry HSDN C0151889 Reflexes tendon increased C1842687 Pontocerebellar hypoplasia type 3 (disorder) MalaCards|HPO C3887638 Failure to thrive in infant C0546264 Congenital fiber type disproportion HPO C2919142 Short stature adverse event C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C0036572 Convulsion C0796200 Wieacker-wolff syndrome MalaCards|UMLS C0036572 Convulsion C3150971 Leopard syndrome 3 MalaCards|HPO C2984058 Have pain C0085648 Synovial cyst HSDN C0009806 Constipate C1548484 Rheumatic fever vaccine HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040411 Tongue neoplasms HSDN C0242936 Center pain C0042580 Vesico-ureteral reflux HSDN C0234146 Absent reflex C0796200 Wieacker-wolff syndrome MalaCards C0015672 Decreased energy C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0018784 Deafness sensorineural C1864436 Muenke syndrome OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0268193 Nadh cytochrome b5 reductase deficiency MalaCards|HPO|UMLS C1145670 Failure respiratory C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C1549543 Administration method - pain C0019522 Adenoma, sweat gland HSDN C0042024 Urine incontinence C0022658 Kidney diseases HSDN C0027796 Neuralgias C0027073 Myofascial pain syndromes HSDN C0007758 Cerebellar ataxia C0344488 Absence; cerebellum OrphaNet C0751837 Gait ataxic C0333157 Colloid cysts HSDN C1962972 Proteinuria adverse event C0017920 Glycogen storage disease type i MalaCards|HSDN|HPO C2911647 Weight gain adverse event C0030636 Pasteurella infection HSDN C4084776 Weight loss C0043253 Trauma blunt HSDN C0031911 Pigment deposition C0334444 Spindle cell melanoma MalaCards C1384666 Decreased hearing C0796070 Microphthalmia, syndromic 7 MalaCards|HPO C0012833 Dizzy C0009324 Ulcerative colitis HSDN C0233514 Behavior abnormal C0752235 Lyme neuroborreliosis MalaCards C0000727 Abdomen acute C0026764 Multiple myeloma HSDN C0042798 Vision dim C1852438 Cataract, coppock-like MalaCards|HPO C1557397 Adverse event associated with pain C0041311 Tuberculosis, female genital HSDN C4023690 Spontaneous pain sensation C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating MalaCards C0151786 Weakness muscle C0034067 Pulmonary emphysema HSDN C4085548 Usual severity dizziness C0085183 Neoplasms, second primary HSDN C0042024 Urine incontinence C2937358 Cerebral hemorrhage HSDN C4084767 Bothered by vomiting C0006145 Breast diseases HSDN C3463815 Feel fatigue C0032269 Pneumococcal infections HSDN C0344315 Mood depressed C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C2984058 Have pain C0031111 Periostitis HSDN C0233565 Bradykinesia C1868596 Atypical parkinson disease HPO C2029884 Hearing loss by exam C0262584 Carcinoma, small cell HSDN C0020649 Blood pressure decreased C1136033 Cutaneous mastocytosis MalaCards C0042755 Virilisation C0001403 Addison disease HSDN C3463815 Feel fatigue C0085183 Neoplasms, second primary HSDN C0522224 Palsied C0014474 Ependymoma HSDN C0151786 Weakness muscle C0729544 Fungal cns infection HSDN C0851578 Disorder sleep C0038525 Subarachnoid hemorrhage HSDN C0016199 Pain flank C3641709 Ensat stage i adrenal cortex carcinoma UMLS C0973461 Dysphasia C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0917816 Deficiency mental C1839321 Scarf syndrome MalaCards C2315100 Pediatric failure to thrive C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0004134 Dyssynergia C1837454 Spinocerebellar ataxia 8 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0026267 Mitral valve prolapse syndrome HSDN C4084784 Diarrhea C0206062 Lung diseases, interstitial HSDN C4085210 Usual severity pain C0010308 Congenital hypothyroidism HSDN C0221752 Rbc urine C1860518 Vasculopathy, retinal, with cerebral leukodystrophy MalaCards|HPO C1549543 Administration method - pain C0020564 Hypertrophy HSDN C0750426 Wbc elevated C0263979 Myositis, purulent MalaCards C0557874 Global developmental delay C0015624 Fanconi syndrome HPO C3539889 Pelvic pain increasing in severity C0017412 Genital diseases, male HSDN C4084766 Vomiting C0024299 Lymphoma HSDN C0349588 Stature short C2675463 Chromosome 15q26-qter deletion syndrome MalaCards C0007859 Pain neck C0004936 Mental disorders HSDN C0004134 Dyssynergia C0342853 Sialuria OrphaNet|MalaCards C4084776 Weight loss C0006145 Breast diseases HSDN C2984058 Have pain C0018671 Head and neck neoplasms HSDN C0036572 Convulsion C1835922 Aminoacylase 1 deficiency MalaCards|HPO|UMLS C0020305 Fetal edema C1419149 Pex2 gene HSDN C0020580 Decreased sensation C0037304 Skull fracture HSDN C0018681 Headache, cephalalgia C0022134 Islet cell adenoma HSDN C0016382 Cutaneous vascular engorgement C3280501 Inflammatory skin and bowel disease, neonatal, 1 MalaCards C0009676 Confusion state C0010346 Crohn disease HSDN C4084769 Vomiting frequency C1856401 Etfa deficiencies HPO C2315100 Pediatric failure to thrive C0268131 Omp decarboxylase deficiency MalaCards C4084802 Usual severity diarrhea C0035412 Rhabdomyosarcoma HSDN C0016199 Pain flank C0242216 Biliary calculi HSDN C1959630 Eye pain adverse event C0015423 Eyelid diseases HSDN C2242996 Tingling C0009324 Ulcerative colitis HSDN C2024878 Cardiovascular surgery result: dyspnea C1969342 Pulmonary hypertension, primary, dexfenfluramine associated HPO C1279888 Proteinuria of undiagnosed cause C0023241 Legionnaires' disease MalaCards C0031911 Pigment deposition C0235974 Pancreatic carcinoma MalaCards C0349588 Stature short C1843418 Niemann-pick disease, type f HPO C3463815 Feel fatigue C1864952 Hyperinsulinemic hypoglycemia, familial, 5 MalaCards C4085642 Level of joint stiffness C2745948 Hyalinosis, systemic MalaCards C0011991 Loose stools C3714535 Malocclusion, angle class ii HSDN C0036572 Convulsion C0795917 Alpha-thalassemia mental retardation syndrome, deletion-type MalaCards C0398650 Idiopathic thrombocytopenia purpura C2937287 Hematolysis HSDN C0027497 Queasy C0812341 Latex allergy response UMLS C0040034 Thrombocytopenia C2675526 Neutropenia, severe congenital, autosomal recessive 4 HPO C0030193 Sense of pain C0080178 Spina bifida HSDN C4084802 Usual severity diarrhea C0007138 Carcinoma, transitional cell HSDN C0020450 Hyperemesis gravidarum C1412000 Mesenteric vascular insufficiency HSDN C0042571 Vertigo subjective C0456892 Csf low pressure HSDN C1069915 Vertigo C0038395 Streptococcal infections HSDN C0740418 Back pain chronic C0006444 Bursitis UMLS C0917816 Deficiency mental C3495551 Dihydropyrimidinuria MalaCards C0030554 Abnormal sensation C0027868 Neuromuscular diseases HSDN C0036572 Convulsion C0852795 Increased insulin level HSDN C1963184 Nystagmus adverse event C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards C1963063 Anorexia adverse event C0024530 Malaria HSDN C4084725 Usual severity cough C0025063 Mediastinal neoplasms HSDN C3887638 Failure to thrive in infant C0033800 Pseudoglioma MalaCards C3887873 Hearing loss C0003838 Arterial occlusive diseases HSDN C0027796 Neuralgias C0033923 Psychomotor function HSDN C0522224 Palsied C0010823 Cytomegalovirus infections HSDN C2096293 Ent surgical result ear vertigo C0015802 Femur fracture HSDN C4084766 Vomiting C0021845 Intestinal perforation HSDN C0009024 Clonus C3807567 Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome MalaCards|UMLS C0039070 Collapse fleeting C0155626 Acute myocardial infarction UMLS C2911645 Weight loss adverse event C1963064 Anxiety adverse event HSDN C3641755 Have constipation C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0010520 Skin cyanosis C0040053 Thrombosis HSDN C1384666 Decreased hearing C1970416 Xfe progeroid syndrome MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0017412 Genital diseases, male HSDN C0005745 Blepharoptosis C0033375 Prolactinoma MalaCards|HPO C0018772 Deafness C0018051 Gonadal dysgenesis HSDN C0151786 Weakness muscle C0036916 Sexually transmitted diseases HSDN C0013911 Emaciate C0035579 Rickets HSDN C0022346 Yellow skin C0011071 Sudden death HSDN C0018772 Deafness C0520946 Emotional hypersensitivity HSDN C3641756 Have diarrhea C1527336 Sjogren's syndrome HSDN C0015230 Exanthem C2931916 Midline granulomatosis MalaCards C4085210 Usual severity pain C0037889 Hereditary spherocytosis HSDN C0024032 Birth weight subnormal C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C0018965 Blood urine C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C1557397 Adverse event associated with pain C0338480 Common migraine HSDN C0014724 Burping C0019284 Diaphragmatic hernia HSDN C2203646 Jaundice C0272126 Evans syndrome OrphaNet|MalaCards C0038002 Spleen enlargement C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO C0085631 Abnormal excitement C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards|HPO|UMLS C0002170 Alopecia disorders C0342861 Uroporphyrinogen decarboxylase deficiency MalaCards C3178766 Nociceptive pain C0037361 Olfactory sense HSDN C1963170 Hypothermia adverse event C0041956 Ureteral obstruction HSDN C1963087 Constipation adverse event C0023467 Leukemia, myelocytic, acute HSDN C0042571 Vertigo subjective C0038525 Subarachnoid hemorrhage HSDN C0013395 Indigestion C0014038 Encephalitis HSDN C1000483 Genus anemia C0281508 Desmoplastic small round cell tumor MalaCards|HPO C2237041 Shox gene with short stature C0268273 Gangliosidosis, generalized gm1, type 3 MalaCards|HPO C0851578 Disorder sleep C0036439 Scoliosis, unspecified HSDN C0012569 Double vision C0006663 Calcinosis HSDN C0012569 Double vision C0040128 Thyroid diseases HSDN C0042963 Symptoms vomiting C0085277 Munchausen by proxy syndrome HSDN C4085211 Pain distress question C0038218 Status asthmaticus HSDN C0003862 Pain joint C0041228 African trypanosomiasis DiseaseOntology C0013395 Indigestion C0033927 Psychopathology HSDN C4084767 Bothered by vomiting C0023374 Lesch-nyhan syndrome MalaCards|HPO C0026821 Cramp C0595812 Fistula route HSDN C3887638 Failure to thrive in infant C1859722 Arthrogryposis renal dysfunction cholestasis syndrome MalaCards|HPO C4084768 Usual severity vomiting C0015408 Eye injury HSDN C0026838 Spasticity muscle C0051981 Anti-leprosy vaccine HSDN C4085661 Usual severity nausea C0020550 Hyperthyroidism HSDN C4042891 Sleep wake disorders C0010598 Cyclothymic disorder HSDN C4084897 Sleep disturbance subordinate domain C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C0018777 Deafness, conductive C0032962 Pregnancy complications HSDN C0242936 Center pain C0019421 Heterosexual behavior HSDN C0034150 Skin purpura C0018924 Hemarthrosis HSDN C1557397 Adverse event associated with pain C0026850 Muscular dystrophy HSDN C0042798 Vision dim C2931291 Familial spastic paraparesis and deafness OrphaNet|MalaCards C1963071 Back pain adverse event C0037205 Sirenomelia HPO C0270948 Neurogenic muscular atrophy C0796136 Ataxia-deafness-retardation syndrome with ketoaciduria MalaCards C2984058 Have pain C0017574 Gingivitis HSDN C0007166 Cardiac output decreased C0344435 Ventricular fibrillation by ecg finding HSDN C4085211 Pain distress question C0014061 Tick-borne encephalitis HSDN C2029884 Hearing loss by exam C1849112 Spastic quadriplegia-retinitis pigmentosa-mental retardation syndrome MalaCards C2911647 Weight gain adverse event C0033906 Psychological theories HSDN C1962972 Proteinuria adverse event C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4084773 Bothered by weight gain C0007134 Renal cell carcinoma HSDN C2911645 Weight loss adverse event C3714514 Infection HSDN C0917816 Deficiency mental C0796206 Atkin syndrome OrphaNet|MalaCards C3539023 Pelvic pain increasing in frequency C0023895 Liver diseases HSDN C4084766 Vomiting C0275911 Tuberculosis of intestines MalaCards C0684343 Pseudophakia C0020581 Blood in anterior chamber HSDN C0018784 Deafness sensorineural C0086431 Hurler-scheie syndrome OrphaNet|HPO C0231807 Dyspnea exertional C0684249 Carcinoma of lung UMLS C0242936 Center pain C0237104 Spirituality HSDN C0018772 Deafness C0001175 Acquired immunodeficiency syndrome HSDN C0002962 Angina C0026782 Mumps vaccine HSDN C0030486 Extremity paralysis, lower C0011570 Mental depression HSDN C0027796 Neuralgias C0700095 Central neuroblastoma HSDN C0004604 Pain back C0038187 Starvation HSDN C0043094 Weight gain C0028758 Bonding HSDN C0020796 Profoundly mentally retarded C2932714 Pontocerebellar hypoplasia type 2 MalaCards C4085210 Usual severity pain C0040948 Trichostrongyliasis HSDN C0022107 Fussiness C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO C2029884 Hearing loss by exam C0039590 Testicular neoplasms HSDN C3539891 Pelvic pain to the rear C0042029 Urinary tract infection HSDN C2107732 Consistent heat intolerance C1706004 Anhydrotic ectodermal dysplasias MalaCards C1549543 Administration method - pain C0008497 Choriocarcinoma HSDN C0018772 Deafness C1418399 Pdb1 gene HPO C0015230 Exanthem C0406242 Acute cheiropodopompholyx UMLS C3898969 Have been vomiting C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0042963 Symptoms vomiting C0020732 Iatrogenic disease HSDN C0520909 Ponv C0023903 Liver neoplasms HSDN C4084802 Usual severity diarrhea C0030846 Penile diseases HSDN C0000727 Abdomen acute C0026848 Myopathy HSDN C0033377 Caudal displacement C0270952 Muscular dystrophy, oculopharyngeal OrphaNet|HPO|MalaCards C2242996 Tingling C1579830 Cutaneous vesicle HSDN C0013404 Respiratory difficulty C3809369 Paroxysmal nocturnal hemoglobinuria 2 MalaCards|UMLS C0013404 Respiratory difficulty C0205788 Histiocytoid hemangioma HSDN C4084776 Weight loss C0037313 Sleep HSDN C4085211 Pain distress question C0042961 Intestinal volvulus HSDN C1549543 Administration method - pain C0001818 Agoraphobia HSDN C1961131 Cough adverse event C0042029 Urinary tract infection HSDN C0042928 Paralysis vocal cord C0027927 Neurosyphilis HSDN C0031315 Phantom limb pain C0037929 Spinal cord injuries HSDN C4084802 Usual severity diarrhea C0009759 Conjunctival diseases HSDN C0086437 Joint hypermobility C0220767 Craniofrontonasal dysplasia HPO|UMLS C0007758 Cerebellar ataxia C1266184 Atypical teratoid/rhabdoid tumor MalaCards C1279888 Proteinuria of undiagnosed cause C0011389 Dental plaque HSDN C0162285 Edema eyelid C1853490 22q13.3 deletion syndrome OrphaNet|HPO|MalaCards C0013395 Indigestion C0041327 Tuberculosis, pulmonary HSDN C0003467 Angst C0221406 Pituitary-dependent cushing's disease OrphaNet|HPO C0413252 Hypothermia due to exposure C0022658 Kidney diseases HSDN C0151311 Cranial nerve palsy C0268390 Muckle-wells syndrome OrphaNet|HPO|MalaCards C4084774 Have weight loss C0004031 Aspergillosis, allergic bronchopulmonary OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0009326 Collagen diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0867389 Chronic graft-versus-host disease MalaCards C0020672 Body temperature decreased C0040046 Thrombophlebitis HSDN C0026838 Spasticity muscle C0016788 Fucosidase deficiency disease OrphaNet|MalaCards C0973461 Dysphasia C0003537 Aphasia MalaCards C3887638 Failure to thrive in infant C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO C0547030 Sensory perceptual alteration: visual C1263864 Blindness and/or vision impairment level UMLS C0018808 Murmur C0003850 Arteriosclerosis HSDN C4084802 Usual severity diarrhea C0002171 Alopecia areata HSDN C0030193 Sense of pain C0282193 Iron overload HSDN C0027796 Neuralgias C0034734 Raynaud disease HSDN C1963086 Confusion adverse event C0162531 Hereditary coproporphyria OrphaNet|HPO C0018777 Deafness, conductive C0001193 Apert syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0030472 Paraneoplastic syndromes HSDN C0018772 Deafness C0011884 Diabetic retinopathy HSDN C0033774 Skin pruritus C0040034 Thrombocytopenia HSDN C0020796 Profoundly mentally retarded C4014488 Pontocerebellar hypoplasia, type 2e MalaCards C0024031 Back pain lower back C0014347 Enterobacteriaceae infections HSDN C0013378 Dysgensia C0030472 Paraneoplastic syndromes HSDN C4084725 Usual severity cough C1322286 Thymoma, type c OrphaNet|MalaCards C0026838 Spasticity muscle C0236969 Substance-related disorders HSDN C0009398 Color vision defects C0017500 Gestalt theories HSDN C0026821 Cramp C0029463 Osteosarcoma HSDN C0036572 Convulsion C1336537 Supratentorial meningioma UMLS C0042963 Symptoms vomiting C0004275 Attitude health HSDN C0522224 Palsied C0006663 Calcinosis HSDN C0010200 Cough symptom C0043253 Trauma blunt HSDN C0039870 Leanness C0233894 Femininity HSDN C4084723 Constipation C0036864 Sexual relations HSDN C0151908 Dry skin C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism OrphaNet|UMLS|MalaCards C0030200 Intractable pain C0004623 Bacterial infections HSDN C0020673 Hypothermia (central) (local) C0038354 Stomach diseases HSDN C0027066 Myoclonic jerking C0796561 Melanoma vaccines HSDN C0030552 Paralysis partial C0025007 Measles HSDN C0233794 Memory impaired C1846564 Spastic paraplegia 7, autosomal recessive MalaCards|HPO C1557397 Adverse event associated with pain C3896673 Familial nonmedullary thyroid gland carcinoma MalaCards C0003862 Pain joint C0014544 Epilepsy HSDN C0426579 Anorexia symptom C0035243 Respiratory tract infections HSDN C0027497 Queasy C0078981 Arachnoid cysts HSDN C0030552 Paralysis partial C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C0575081 Abnormal gait C2677567 Dystonia 16 (disorder) MalaCards|HPO C0004134 Dyssynergia C0796561 Melanoma vaccines HSDN C3665492 Pigmentations C3272841 Mutyh-associate polyposis MalaCards C4085549 Dizziness C0011581 Depressive disorder HSDN C1961131 Cough adverse event C0206138 Crest syndrome MalaCards C1963087 Constipation adverse event C0035934 Rubinstein-taybi syndrome OrphaNet|HPO|MalaCards C3665347 Vision impaired C2751308 Cone dystrophy 4 (disorder) MalaCards|HPO C0042024 Urine incontinence C0751603 Autosomal recessive hereditary spastic paraplegia MalaCards C0522224 Palsied C0041834 Erythema HSDN C0576456 Poor feeding C3203358 Hypoventilation MalaCards C0013404 Respiratory difficulty C0003850 Arteriosclerosis HSDN C0019825 Voice hoarseness C1853578 Neuroferritinopathy OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0161408 Cranial nerve vii injuries HSDN C0036572 Convulsion C0812437 Oculo-dento-digital syndrome OrphaNet|UMLS|HPO|MalaCards C0018772 Deafness C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C0043094 Weight gain C0021831 Intestinal diseases HSDN C0241137 Skin pallor C0149573 Structure of posterior inferior cerebellar artery HSDN C0271215 Blindness legal C0206307 Canavan disease OrphaNet|HPO|MalaCards C0030975 Disorders perception C0043097 Perception, weight HSDN C1519353 Skin eruption papular C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0009806 Constipate C1253943 Fluid in the chest HSDN C0454644 Delayed language development C0265245 Nager syndrome OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1839530 Valproate sensitivity HPO C0027796 Neuralgias C0036974 Shock HSDN C3463815 Feel fatigue C0152171 Idiopathic pulmonary hypertension OrphaNet C0030552 Paralysis partial C2984572 Malaria pathway HSDN C0027497 Queasy C1866552 Paragangliomas 2 (disorder) MalaCards C0003862 Pain joint C0017205 Gaucher disease OrphaNet|MalaCards C0002965 Crescendo angina C0040038 Thromboembolism HSDN C0152227 Tearing excessive C0339284 Polymorphous corneal dystrophy MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0032343 Poisoning HSDN C0036572 Convulsion C1848913 Tay-sachs disease, juvenile HPO C0020673 Hypothermia (central) (local) C0342443 Adrenal cushing's syndrome HSDN C4085210 Usual severity pain C0085293 Hepatitis e HSDN C2096293 Ent surgical result ear vertigo C0010709 Cyst HSDN C1963091 Diarrhea adverse event C0039446 Telangiectasis HSDN C0030552 Paralysis partial C0162820 Dermatitis, allergic contact HSDN C4085661 Usual severity nausea C0027831 Neurofibromatosis 1 HSDN C4084774 Have weight loss C0024419 Waldenstrom macroglobulinemia HSDN C2919142 Short stature adverse event C1857550 11-beta-hydroxysteroid dehydrogenase, type ii HPO C0027497 Queasy C0011849 Diabetes mellitus HSDN C0015230 Exanthem C0011615 Dermatitis, atopic UMLS C0040822 D tremors C0751871 Autoimmune diseases of the nervous system HSDN C0016382 Cutaneous vascular engorgement C0265336 Senter syndrome OrphaNet|HPO|MalaCards C0019209 Large liver C0029106 Opisthorchiasis DiseaseOntology C1963091 Diarrhea adverse event C0019159 Hepatitis a HSDN C0026826 High muscle tone C0751870 Heredodegenerative disorders, nervous system HSDN C4085317 Diarrhea frequency C0242966 Systemic inflammatory response syndrome HSDN C0011168 Disorder deglutition C1853926 Nonaka myopathy MalaCards C0004134 Dyssynergia C1963229 Retinal detachment adverse event HSDN C0040822 D tremors C0699828 Serotonergic syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0039504 Injuries tendon HSDN C4084766 Vomiting C0035801 Diseases rodent HSDN C0036572 Convulsion C1275079 Acps iii MalaCards C4084773 Bothered by weight gain C0079487 Helicobacter infections HSDN C0009806 Constipate C0242343 Panhypopituitarism MalaCards|HPO C1557397 Adverse event associated with pain C0043540 Zygomatic fracture HSDN C0027066 Myoclonic jerking C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0030232 Color loss C1264008 Chronic cold agglutinin disease MalaCards C0041105 Jaw spasm C0009917 Contracture HSDN C0427055 Face weakness C3648263 Late effects of nontraumatic intracerebral hemorrhage facial weakness UMLS C2911645 Weight loss adverse event C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0018571 Hand injury HSDN C4085222 Nausea C1962979 Burn adverse event HSDN C0019825 Voice hoarseness C1336482 Stage i small cell carcinoma of lung UMLS C0557874 Global developmental delay C1844836 Ayazi syndrome MalaCards C0349588 Stature short C2748571 Isolated growth hormone deficiency, type ib HPO C2911647 Weight gain adverse event C0024305 Lymphoma, non-hodgkin HSDN C0013421 Dystonia C1291512 Beta-ureidopropionase deficiency MalaCards|HPO C0033774 Skin pruritus C0017658 Glomerulonephritis HSDN C2875332 Spastic hemiplegia affecting right nondominant side C0154694 Spastic hemiplegia UMLS C4085317 Diarrhea frequency C0031039 Effusion pericardial HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1306577 Dies patient HSDN C4084774 Have weight loss C3541306 Plasmodium measurement HSDN C3665347 Vision impaired C0221061 Behr syndrome OrphaNet|HPO C0018834 Brash C0041327 Tuberculosis, pulmonary HSDN C0040485 Wryneck C0040425 Tonsillitis HSDN C0237326 Defecation pain C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0037763 Spasm C2586211 Thrombosis of blood vessel HSDN C0232726 Tenesmus, rectal C1970820 Fabry disease, cardiac variant HPO C0241137 Skin pallor C0038002 Splenomegaly HSDN C0018784 Deafness sensorineural C2751843 Leukoencephalopathy, cystic, without megalencephaly MalaCards|HPO C0027066 Myoclonic jerking C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO|UMLS C0019521 Hiccoughs C4049644 Depression HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020435 Hyperbilirubinemia, hereditary HSDN C1850830 Exercise-induced muscle pain C0017924 Glycogen storage disease type v HPO C4084727 Cough frequency C0748164 Pulmonary nodule multiple HSDN C0015672 Decreased energy C0024620 Primary malignant neoplasm of liver MalaCards C0917816 Deficiency mental C1866495 Bartter syndrome, antenatal type 1 HPO C0000727 Abdomen acute C0027666 Neoplasms, radiation-induced HSDN C0000737 Abdomen pain C2981668 Stage iii distal bile duct cancer UMLS C0085636 Light sensitivity C4225315 Retinitis pigmentosa 72 UMLS C0007758 Cerebellar ataxia C0020443 Hypercholesterolemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030271 Pancoast syndrome HSDN C4085211 Pain distress question C0398738 Leukocyte adhesion deficiency type 1 MalaCards C0151786 Weakness muscle C0751795 Head injury penetrating HSDN C0460137 Push down or depress C0020179 Huntington disease MalaCards|HPO C0522224 Palsied C0027726 Nephrotic syndrome HSDN C0026838 Spasticity muscle C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C0015468 Face pain C0024305 Lymphoma, non-hodgkin HSDN C3898969 Have been vomiting C0035066 Renal artery obstruction HSDN C0036572 Convulsion C0795851 14 trisomy mosaicism syndrome OrphaNet|MalaCards C0010520 Skin cyanosis C0037369 Smoking HSDN C0013362 Dysarthrias C0024299 Lymphoma HSDN C1963091 Diarrhea adverse event C0007766 Intracranial aneurysm HSDN C0005745 Blepharoptosis C0795902 Coloboma, cleft lip-palate and mental retardation syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0001807 Aggressive behavior HSDN C0019209 Large liver C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0014118 Inflammation of the heart valve C0003507 Aortic valve stenosis MalaCards C0018784 Deafness sensorineural C1963064 Anxiety adverse event HSDN C0026838 Spasticity muscle C0042018 Urinary calculi HSDN C0000737 Abdomen pain C0018621 Hay fever HSDN C0002962 Angina C0025007 Measles HSDN C4084726 Distress cough C0014859 Esophageal neoplasms OrphaNet|HSDN|MalaCards C4084774 Have weight loss C1527311 Brain edema HSDN C3274924 Have been coughing C0020523 Immediate hypersensitivity HSDN C4084766 Vomiting C0007786 Brain ischemia HSDN C0023012 Delay language C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C0917816 Deficiency mental C1832408 Hunter-mcalpine craniosynostosis syndrome MalaCards C0020455 Hypergammaglobulinemia C0009782 Connective tissue diseases HSDN C0012833 Dizzy C0395932 Episodic recurrent vertigo UMLS C4085210 Usual severity pain C0014866 Esophageal stenosis HSDN C0043094 Weight gain C0027055 Myocardial reperfusion injury HSDN C4085210 Usual severity pain C0700251 Brachial plexus neuropathies HSDN C0151786 Weakness muscle C0238111 Lennox-gastaut syndrome HSDN C0018772 Deafness C0033873 Psychiatry HSDN C0242936 Center pain C0425045 Sudden infant death HSDN C0003469 Anxiety disorder C0393639 Hashimoto's encephalitis MalaCards C0030232 Color loss C0038002 Splenomegaly HSDN C2830325 Other abnormalities of gait and mobility C0154725 Oth disorder nervous system UMLS C0010520 Skin cyanosis C0022665 Kidney neoplasm HSDN C0018784 Deafness sensorineural C1857750 Deafness, autosomal recessive 66 MalaCards|HPO C4084784 Diarrhea C0009447 Common variable immunodeficiency HPO C0020673 Hypothermia (central) (local) C0003504 Aortic valve insufficiency HSDN C2024893 Cardiovascular surgery result: fatigue C2316212 Cryopyrin-associated periodic syndromes MalaCards C0013404 Respiratory difficulty C1336435 Stage iv mesothelioma of pleura UMLS C2984058 Have pain C0024314 Lymphoproliferative disorders HSDN C2984058 Have pain C0027720 Nephrosis HSDN C4084769 Vomiting frequency C4015130 Inflammatory skin and bowel disease, neonatal, 2 MalaCards C3641756 Have diarrhea C0001261 Actinomycosis HSDN C3274924 Have been coughing C0040128 Thyroid diseases HSDN C1963091 Diarrhea adverse event C1956257 Pulmonary stenosis HSDN C0015469 Facial paralysis C0014591 Epistaxis HSDN C0018777 Deafness, conductive C0037286 Skin neoplasms HSDN C0009421 Comatose C0011884 Diabetic retinopathy HSDN C0042025 Urinary incontinence stress C1269683 Major depressive disorder HSDN C0027796 Neuralgias C2911643 Encounter due to family history of osteoporosis HSDN C0019209 Large liver C3888244 Aicardi-goutieres syndrome 7 MalaCards C2315100 Pediatric failure to thrive C1260899 Anemia, diamond-blackfan HPO C0002962 Angina C0162820 Dermatitis, allergic contact HSDN C0917816 Deficiency mental C0796092 Oculo-cerebro-cutaneous syndrome OrphaNet|MalaCards C3541349 Syncope C1269683 Major depressive disorder HSDN C0020455 Hypergammaglobulinemia C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C2032395 Pelvic pain on the left C0037274 Dermatologic disorders HSDN C0155536 Paracousis C0375257 Auditory perception and discrimination disorders UMLS C0003811 Cardiac rhythm disturbance C1868390 Facioauriculoradial dysplasia OrphaNet|MalaCards C4085211 Pain distress question C0040583 Tracheal stenosis HSDN C0043068 Friderichsen-waterhouse syndrome C0027651 Tumor HSDN C0036572 Convulsion C1834673 Facioscapulohumeral muscular dystrophy 1a MalaCards|HPO C4085211 Pain distress question C0021432 Infratentorial neoplasms HSDN C3898969 Have been vomiting C0887833 Carcinoma, pancreatic ductal HSDN C0151786 Weakness muscle C0022716 Menkes kinky hair syndrome OrphaNet|HPO|MalaCards C3665386 Abnormal vision C1568248 Usher syndrome, type iii OrphaNet|HPO C0030975 Disorders perception C0038436 Post-traumatic stress disorder HSDN C0035078 Failure kidney C1850331 Oculorenocerebellar syndrome OrphaNet|MalaCards C0003079 Pupillary inequality C0029124 Optic atrophy HSDN C0460137 Push down or depress C1861457 Progressive encephalomyelitis with rigidity MalaCards C4042891 Sleep wake disorders C0020538 Hypertensive disease HSDN C0520559 Numbness tongue C0040409 Tongue diseases UMLS C1963087 Constipation adverse event C0014170 Endometrial neoplasms HSDN C4085317 Diarrhea frequency C1832370 Myopathy, myofibrillar, desmin-related MalaCards|HPO C0231528 Muscle pain generalized C2936881 Eosinophilic synovitis MalaCards C1963087 Constipation adverse event C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO C3641756 Have diarrhea C0347555 Friction blister HSDN C0016382 Cutaneous vascular engorgement C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C0004093 Asthenia C0037050 Sick building syndrome HSDN C1963091 Diarrhea adverse event C0030489 Paraproteinemias HSDN C0520909 Ponv C0428977 Bradycardia HSDN C0042798 Vision dim C0206307 Canavan disease OrphaNet C2242996 Tingling C0344434 Atrial fibrillation ecg HSDN C0151786 Weakness muscle C0010356 Cross infection HSDN C0426579 Anorexia symptom C0011881 Diabetic nephropathy HSDN C0004134 Dyssynergia C0029125 Optic atrophies, hereditary HSDN C4084766 Vomiting C0022821 Kyphosis deformity of spine HSDN C4085317 Diarrhea frequency C0006625 Cachexia HSDN C0027796 Neuralgias C0037274 Dermatologic disorders HSDN C0221166 Paraparesis C0026470 Monoclonal gammopathy of undetermined significance HSDN C0026821 Cramp C3495427 Fanconi-bickel syndrome MalaCards C2919142 Short stature adverse event C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C0005904 Alteration in body temperature C3203358 Hypoventilation MalaCards C0008031 Pain chest C0016842 Congenital pectus excavatum HSDN C0000727 Abdomen acute C1306503 Congenital exomphalos HSDN C4085317 Diarrhea frequency C1306577 Dies patient HSDN C3641756 Have diarrhea C1862892 Hereditary angioedema type ii HPO C0221166 Paraparesis C0035053 Spontaneous remission HSDN C1963180 Neck pain adverse event C0221204 Lytic lesion HSDN C0015230 Exanthem C0019100 Severe dengue OrphaNet C4085222 Nausea C0024266 Lymphocytic choriomeningitis DiseaseOntology|MalaCards C4085210 Usual severity pain C0040761 Transposition of great vessels HSDN C0015672 Decreased energy C0062527 Hepatitis b vaccine HSDN C0003811 Cardiac rhythm disturbance C0271972 Thiamine-responsive megaloblastic anemia MalaCards C4085211 Pain distress question C0030286 Pancreatic diseases HSDN C2919142 Short stature adverse event C2936915 Amylo-1,6-glucosidase deficiency OrphaNet|HPO C0013604 Edematous C0302497 Retrobulbar haemorrhage HSDN C0018772 Deafness C0265205 Robinow syndrome MalaCards C2237041 Shox gene with short stature C2363065 Vitamin d-resistant rickets OrphaNet|MalaCards C0018772 Deafness C0428977 Bradycardia HSDN C4084727 Cough frequency C0002874 Aplastic anemia HSDN C0018772 Deafness C0034960 Refsum disease HSDN C4085210 Usual severity pain C0029185 Orbit tumor HSDN C1549543 Administration method - pain C0022362 Jaw diseases HSDN C4084768 Usual severity vomiting C1857855 Spastic paraplegia 29, autosomal dominant MalaCards C4018871 Abnormality of the respiratory system C0431406 Asymmetric crying face association MalaCards C1963065 Apnea adverse event C0014836 Escherichia coli infections HSDN C0010038 Corneal opacity disorder C1837884 Larsen-like syndrome MalaCards C4085317 Diarrhea frequency C0014849 Esophageal and gastric varices HSDN C0232854 Urinary stream, slowing of C0810038 Genitourinary symptoms and ill-defined conditions UMLS C4084776 Weight loss C0852007 Scleroderma and associated disorders OrphaNet C0812426 Kidney problem C0027721 Lipoid nephrosis UMLS C0085593 Chill C1336312 Stage ii mesothelioma of pleura UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0031212 Personality disorders HSDN C1549543 Administration method - pain C0016659 Close fracture HSDN C0007758 Cerebellar ataxia C0037773 Spastic paraplegia, hereditary OrphaNet|HSDN|MalaCards C0007384 Cataplexy C0007384 Cataplexy HPO C0027066 Myoclonic jerking C0206729 Neurofibrosarcoma HSDN C0000727 Abdomen acute C0162871 Aortic aneurysm, abdominal HSDN C1963087 Constipation adverse event C0850803 Anaphylaxis (non medication) HSDN C0812426 Kidney problem C0017668 Focal glomerulosclerosis UMLS C0018808 Murmur C0004239 Atrial flutter HSDN C0019572 Hairiness C0005891 Bodies image HSDN C3887638 Failure to thrive in infant C0751273 Infantile globoid cell leukodystrophy MalaCards C0019209 Large liver C1415614 Hmgcl gene HPO C0349588 Stature short C1833454 Komuragaeri disease OrphaNet|MalaCards C4084774 Have weight loss C0008354 Cholera HSDN C2024893 Cardiovascular surgery result: fatigue C0752287 Sleep disorders, intrinsic HSDN C0234146 Absent reflex C3553656 Dhmn vb MalaCards C0018681 Headache, cephalalgia C0005891 Bodies image HSDN C4084792 Usual severity hair loss C1846142 Hoyeraal-hreidarsson syndrome MalaCards C0022346 Yellow skin C0023364 Leptospirosis DiseaseOntology|MalaCards C0234146 Absent reflex C2750537 Myopathy, actin, congenital, with cores HPO C3539889 Pelvic pain increasing in severity C0040053 Thrombosis HSDN C2984058 Have pain C1720830 Painful bladder syndrome OrphaNet|MalaCards C0013390 Cramps menstrual C0004096 Asthma HSDN C0042025 Urinary incontinence stress C0012979 Canine disease HSDN C3539889 Pelvic pain increasing in severity C0042063 Urogenital abnormalities HSDN C4084802 Usual severity diarrhea C0032045 Placenta disorders HSDN C0013404 Respiratory difficulty C0242855 Congenital atresia of pulmonary valve HSDN C3463815 Feel fatigue C0005956 Bone marrow diseases HSDN C0015672 Decreased energy C0086543 Cataract nos HSDN C0026826 High muscle tone C3554499 Microcephaly 10, primary, autosomal recessive MalaCards C0020438 Hypercalciuria C0860549 Refeed syndrome HSDN C0015799 Feminisation C0041408 Turner syndrome HSDN C1963086 Confusion adverse event C0878576 Posterior leucoencephalopathy syndrome HSDN C0460137 Push down or depress C1856491 Gaucher disease, type iiia HPO C4084776 Weight loss C0238358 Hypokalemic periodic paralysis HSDN C0024031 Back pain lower back C0019112 Hemorrhoids HSDN C0427055 Face weakness C4225369 Myasthenic syndrome, congenital, 4b, fast-channel UMLS C2024893 Cardiovascular surgery result: fatigue C0019284 Diaphragmatic hernia HSDN C0009676 Confusion state C0036980 Shock, cardiogenic HSDN C0030486 Extremity paralysis, lower C0021933 Intussusception HSDN C0018784 Deafness sensorineural C0266004 Knuckle pads, leuconychia and sensorineural deafness OrphaNet|HPO|MalaCards C0027497 Queasy C0556520 Psychological desensitization HSDN C2911647 Weight gain adverse event C0035358 Retroperitoneal neoplasm HSDN C0033774 Skin pruritus C0013502 Echinococcosis HSDN C3665347 Vision impaired C1832440 Microphthalmia, syndromic 8 OrphaNet|MalaCards C4084768 Usual severity vomiting C0010674 Cystic fibrosis HSDN C2315100 Pediatric failure to thrive C2930798 Alexanders leukodystrophy MalaCards C4084727 Cough frequency C0030807 Pemphigus, nos HSDN C0018784 Deafness sensorineural C0032460 Polycystic ovary syndrome HSDN C0034150 Skin purpura C4049644 Depression HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0007273 Carotid artery diseases HSDN C0042024 Urine incontinence C1846046 Spastic paraplegia 16, x-linked (disorder) MalaCards C0042024 Urine incontinence C0023055 Laryngeal neoplasm HSDN C4084774 Have weight loss C0848377 Trauma to the abdomen HSDN C3898969 Have been vomiting C1367460 Lats1 gene HSDN C0018772 Deafness C0013336 Dwarfism HSDN C3541349 Syncope C0016658 Fracture bone HSDN C1963281 Vomiting adverse event C0022661 Kidney failure, chronic HSDN C0042940 Disorder of voice C0460137 Push down or depress HSDN C1319543 On examination - right eye diabetic maculopathy C1532602 Diabetic retinopathy with clinically significant macular edema in right eye UMLS C1279888 Proteinuria of undiagnosed cause C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C0016199 Pain flank C0031036 Polyarteritis nodosa HSDN C0004604 Pain back C0009946 Conversion disorder HSDN C0000737 Abdomen pain C0020517 Hypersensitivity HSDN C3539890 Pelvic pain causes awakening at night C0029456 Osteoporosis HSDN C2242996 Tingling C0027643 Neoplasm recurrence, local HSDN C0270790 Quadriparesis C1833603 Spondyloepiphyseal dysplasia with atlantoaxial instability MalaCards|UMLS C0037771 Paraparesis spastic C0005697 Neurogenic urinary bladder UMLS C3887784 Decreased urine output C0020437 Hypercalcemia HSDN C1279888 Proteinuria of undiagnosed cause C0041374 Tumor virus infections HSDN C0030554 Abnormal sensation C0012979 Canine disease HSDN C2024893 Cardiovascular surgery result: fatigue C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0700078 Deep tendon reflex decrease C0024814 Marinesco-sjogren syndrome MalaCards C0004941 Behavioral symptoms C2675857 Holoprosencephaly 10 MalaCards C1963091 Diarrhea adverse event C0006277 Bronchitis HSDN C4084723 Constipation C0035229 Respiratory insufficiency HSDN C1384666 Decreased hearing C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C0018991 Paralysis one side of body C0037926 Compression of spinal cord HSDN C0853945 Oral mucosa blister C0079297 Epidermolysis bullosa progressiva HPO C1963170 Hypothermia adverse event C0008065 Childhood behavior HSDN C0017181 Gastrointestinal bleed C0037661 Somatostatinoma MalaCards C2984058 Have pain C0085082 Fungemia HSDN C0007758 Cerebellar ataxia C0020517 Hypersensitivity HSDN C2315100 Pediatric failure to thrive C3810043 Immunodeficiency 15 MalaCards C0518090 Frequency of pain question C0026847 Spinal muscular atrophy HSDN C0043094 Weight gain C0085271 Self-injurious behavior HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026528 Moral code HSDN C0028738 Nystagmus C0342683 Albinism, oculocutaneous, type iii OrphaNet|HPO|MalaCards C0019521 Hiccoughs C0001403 Addison disease HSDN C0518090 Frequency of pain question C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C4084802 Usual severity diarrhea C0029408 Degenerative polyarthritis HSDN C0011991 Loose stools C0008065 Childhood behavior HSDN C1549543 Administration method - pain C0032131 Plasmacytoma HSDN C1963087 Constipation adverse event C0017181 Gastrointestinal hemorrhage HSDN C1963091 Diarrhea adverse event C2984572 Malaria pathway HSDN C4084784 Diarrhea C0003872 Arthritis, psoriatic HSDN C4085862 Bothered by nausea C0026769 Multiple sclerosis HSDN C0034150 Skin purpura C0343208 Essential mixed cryoglobulinemia OrphaNet|MalaCards C0037771 Paraparesis spastic C1527336 Sjogren's syndrome HSDN C4085317 Diarrhea frequency C0018824 Heart valve disease HSDN C0000737 Abdomen pain C1266026 Gastric parietal cell adenocarcinoma UMLS C2919142 Short stature adverse event C1851801 Eds viib OrphaNet|HPO C2024893 Cardiovascular surgery result: fatigue C1547940 Specimen source codes - ulcer HSDN C4085317 Diarrhea frequency C2931876 Hirschsprung disease 1 MalaCards C0013404 Respiratory difficulty C0024636 Malocclusion HSDN C2024878 Cardiovascular surgery result: dyspnea C0037397 Behavior social HSDN C1963180 Neck pain adverse event C0027663 Neoplasms, multiple primary HSDN C4084767 Bothered by vomiting C0019310 Hernia, obturator HSDN C2024878 Cardiovascular surgery result: dyspnea C0026650 Movement disorders HSDN C0019825 Voice hoarseness C0003810 Sertoli-leydig cell tumor of ovary UMLS C0002622 Amnesias C0024121 Lung neoplasms HSDN C1384666 Decreased hearing C1834711 Cerebelloparenchymal disorder vi MalaCards|HPO C0042024 Urine incontinence C0752347 Lewy body disease HSDN C1963252 Tremor adverse event C3495422 Finding relating to sexuality and sexual activity HSDN C1549543 Administration method - pain C0679360 Foodborne disease HSDN C0004604 Pain back C0549567 Pigmentation disorders HSDN C1963091 Diarrhea adverse event C0018944 Hematoma HSDN C0015469 Facial paralysis C0017658 Glomerulonephritis HSDN C4084766 Vomiting C0043241 Wound infection HSDN C0018777 Deafness, conductive C0008441 Chondroblastoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0037047 Sibling HSDN C0020673 Hypothermia (central) (local) C0037274 Dermatologic disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018944 Hematoma HSDN C2984058 Have pain C0010967 Behavior, dangerous HSDN C0009806 Constipate C0022408 Arthropathy HSDN C0518090 Frequency of pain question C0039131 Syphilis congenital HSDN C0018834 Brash C1956346 Coronary artery disease HSDN C0004134 Dyssynergia C0041948 Uremia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003886 Arthrogryposis HSDN C3815497 Cough C0011881 Diabetic nephropathy HSDN C0015468 Face pain C0035435 Rheumatism HSDN C0240715 Perineal lump C0685199 Neoplasm - soft tissue types blood vessel malignant of pelvis perineum secondary UMLS C0000727 Abdomen acute C0001403 Addison disease HSDN C2237041 Shox gene with short stature C0086626 Minamata disease OrphaNet C0497247 Blood pressure elevation C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C0011991 Loose stools C0020757 Ichthyoses HSDN C3665386 Abnormal vision C0242383 Age related macular degeneration MalaCards C0401020 Intra-abdominal collection C2919725 Accumulation of bile in abdominal cavity UMLS C4049644 Depression C0162531 Hereditary coproporphyria OrphaNet|HPO C3539889 Pelvic pain increasing in severity C0009404 Colorectal neoplasms HSDN C0023012 Delay language C0394006 Dysequilibrium syndrome HPO C3898969 Have been vomiting C0039730 Thalassemia HSDN C0020305 Fetal edema C0267372 Intestinal lymphatic obstruction MalaCards C0039070 Collapse fleeting C2678477 Brugada syndrome 4 MalaCards|HPO C0232608 Nose regurgitation C0264387 Pneumonia aspiration due to regurgitated food UMLS C0019209 Large liver C1304205 Neutrophilic urticaria MalaCards C0043094 Weight gain C0021361 Female infertility HSDN C0002963 Angina variant C0852795 Increased insulin level HSDN C0013404 Respiratory difficulty C0520946 Emotional hypersensitivity HSDN C0042928 Paralysis vocal cord C0032927 Precancerous conditions HSDN C0243026 Generalized infection C0086438 Hypogammaglobulinemia MalaCards C4085222 Nausea C0002453 Amenorrhea HSDN C0040264 Ear ringing sound C0302148 Blood clot HSDN C1549543 Administration method - pain C0029877 Ear inflammation HSDN C4085549 Dizziness C0040034 Thrombocytopenia HSDN C0036572 Convulsion C1859228 Cerebrohepatorenal syndrome, variant types HPO C0020305 Fetal edema C2931241 Primary intestinal lymphangiectasis MalaCards C0000737 Abdomen pain C1333088 Colonic hamartomatous polyps MalaCards C0036572 Convulsion C3697634 Post infectious grand mal epilepsy UMLS C0035229 Respiratory function impaired C1510455 Acrocephalosyndactylia MalaCards|HPO C0023015 Language handicap C0024530 Malaria HSDN C0033774 Skin pruritus C1963198 Pancreatitis adverse event HSDN C0233844 Awkwardness C0853240 Mobius ii syndrome MalaCards C0020305 Fetal edema C0018995 Hemochromatosis HSDN C2315100 Pediatric failure to thrive C3553960 Peroxisome biogenesis disorder 8b MalaCards C0013362 Dysarthrias C0031345 Pharyngeal diseases HSDN C0020672 Body temperature decreased C0020621 Hypokalemia HSDN C0028961 Urine output decreased C0242966 Systemic inflammatory response syndrome HSDN C0002622 Amnesias C0020494 Hyperostosis frontalis interna HSDN C0007758 Cerebellar ataxia C0037341 Slow virus diseases HSDN C0028738 Nystagmus C0268238 Triglyceride storage disease with ichthyosis MalaCards|HPO C0587047 Mass of trunk C0266800 Polyp; umbilical UMLS C0043094 Weight gain C0016470 Food allergy HSDN C0030200 Intractable pain C0043253 Trauma blunt HSDN C0557874 Global developmental delay C1864871 Chromosome 17q21.31 deletion syndrome OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C4084723 Constipation C0236969 Substance-related disorders HSDN C3641755 Have constipation C3553960 Peroxisome biogenesis disorder 8b MalaCards C0004604 Pain back C4087096 Childhood myxopapillary ependymoma UMLS C2315100 Pediatric failure to thrive C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C0917816 Deficiency mental C1849332 Rodrigues blindness OrphaNet|MalaCards C0002962 Angina C0008149 Chlamydia infections HSDN C0349506 Sun sensitivity C3280721 Chilblain lupus 2 MalaCards C0036572 Convulsion C0221757 Alpha 1-antitrypsin deficiency HSDN C2024893 Cardiovascular surgery result: fatigue C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0034933 Abnormal reflexes C0004782 Basal ganglia diseases HSDN C1279888 Proteinuria of undiagnosed cause C0030297 Pancreatic neoplasm HSDN C2984057 Have nausea C4050613 Anxiety scale (basc-2) HSDN C0007758 Cerebellar ataxia C0751291 Desmoplastic medulloblastoma MalaCards C0036572 Convulsion C0677607 Hashimoto disease HSDN C3463815 Feel fatigue C0006114 Cerebral edema HSDN C2911645 Weight loss adverse event C3463824 Myelodysplastic syndrome HSDN C0007642 Cellulitis nos C0221026 X-linked agammaglobulinemia OrphaNet|HPO C1963091 Diarrhea adverse event C0006818 Campylobacter infection DiseaseOntology C4084766 Vomiting C0032827 Potassium deficiency HSDN C0027497 Queasy C0162565 Acute intermittent porphyria MalaCards|HPO|UMLS C0018784 Deafness sensorineural C0037369 Smoking HSDN C0000727 Abdomen acute C0021828 Intestinal atresia HSDN C4084767 Bothered by vomiting C0027121 Myositis HSDN C0522224 Palsied C0040435 Tooth diseases HSDN C0494475 Seizure generalized tonic clonic C3151229 Febrile seizures, familial, 3b HPO C0042025 Urinary incontinence stress C0017181 Gastrointestinal hemorrhage HSDN C0086565 Liver function abnormal C3279964 Hyperbiliverdinemia MalaCards C0851578 Disorder sleep C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C3641755 Have constipation C0001175 Acquired immunodeficiency syndrome HSDN C0007758 Cerebellar ataxia C0796117 Pitt syndrome MalaCards C0015938 Fetal macrosomia C0023903 Liver neoplasms HSDN C0016199 Pain flank C0007134 Renal cell carcinoma UMLS C1069915 Vertigo C3151295 Hypomagnesemia 6, renal MalaCards|HPO C0237849 Skin desquamation C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C4085642 Level of joint stiffness C0796081 Growth mental deficiency syndrome of myhre MalaCards C0015230 Exanthem C0011620 Stasis dermatitis UMLS C0009398 Color vision defects C0001175 Acquired immunodeficiency syndrome HSDN C0424755 Fever symptoms C0017185 Gastrointestinal neoplasms HSDN C0018784 Deafness sensorineural C0751955 Brain infarction HSDN C0011991 Loose stools C0038012 Spondylitis HSDN C1963281 Vomiting adverse event C0041327 Tuberculosis, pulmonary HSDN C0012569 Double vision C0338437 Neurocysticercosis HSDN C4084802 Usual severity diarrhea C0040592 Trachoma HSDN C0031154 Peritonitis, nos C0398763 Factor b deficiency MalaCards C0038002 Spleen enlargement C0238386 Cronkhite-canada disease MalaCards C1510456 Wernicke aphasia C0009241 Cognition disorders HSDN C0557874 Global developmental delay C3150675 Chromosome 15q24 duplication syndrome HPO C0241165 Skin thickening C0001206 Acromegaly OrphaNet|MalaCards C0751495 Seizure focal C0349604 Intracranial meningioma MalaCards C0162298 Stiffness joints C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0015672 Decreased energy C0517555 Venous thrombosis after immobility HSDN C0332563 Papulae C0023281 Leishmaniasis OrphaNet|MalaCards C0042024 Urine incontinence C1090821 Sepsis (invertebrate) HSDN C3815497 Cough C0006434 Burn injury HSDN C0040034 Thrombocytopenia C1855116 Methylmalonic aciduria, mut(-) type HPO C0007758 Cerebellar ataxia C0009375 Colonic neoplasms HSDN C4085548 Usual severity dizziness C0002351 Altitude sickness HSDN C1962972 Proteinuria adverse event C0008626 Congenital chromosomal disease HSDN C1963091 Diarrhea adverse event C1833275 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative HPO C1828863 Dry cough pharmaceutical C0023240 Legionellosis DiseaseOntology C3539889 Pelvic pain increasing in severity C3495422 Finding relating to sexuality and sexual activity HSDN C0042024 Urine incontinence C0342613 Danish type familial amyloid cardiomyopathy MalaCards C3539893 Pelvic pain occurs with intercourse C0269185 Uterus retroverted HSDN C0008031 Pain chest C1963119 Stomach ulcer adverse event HSDN C0015672 Decreased energy C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C0042928 Paralysis vocal cord C0037305 Neoplasm, skull HSDN C1971624 Appetite absent C0023241 Legionnaires' disease MalaCards C0000731 Abdomen distention C1578691 Congenital myxedema MalaCards C0027498 Nausea vomiting C0235387 Porphyria type syndrome OrphaNet C0041657 Consciousness loss C1458155 Mammary neoplasms HSDN C0018772 Deafness C0008526 Choroiditis HSDN C4042891 Sleep wake disorders C0524851 Neurodegenerative disorders HSDN C0014089 Functional encopresis C0027932 Neurotic disorders HSDN C1963091 Diarrhea adverse event C0085389 Bacillaceae infection HSDN C0497247 Blood pressure elevation C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0011432 Dentin hypersensitivity HSDN C4084725 Usual severity cough C0021400 Influenza DiseaseOntology|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0031049 Tuberculous pericarditis HSDN C0019521 Hiccoughs C0024923 Death maternal HSDN C0012833 Dizzy C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C1963281 Vomiting adverse event C0162871 Aortic aneurysm, abdominal HSDN C0012833 Dizzy C0002395 Alzheimer's disease HSDN C4085661 Usual severity nausea C0028738 Nystagmus HSDN C0014591 Bleeding nose C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards|HPO C3829611 Nausea frequency C1961100 Erectile dysfunction adverse event HSDN C4085317 Diarrhea frequency C0030330 Panniculitis, peritoneal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014805 Primary erythermalgia HPO C0036572 Convulsion C0742470 Cns lesion ring enhancing UMLS C0040264 Ear ringing sound C0027663 Neoplasms, multiple primary HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017160 Gastroenteritis HSDN C2024893 Cardiovascular surgery result: fatigue C0027697 Nephritis HSDN C0917816 Deficiency mental C0265336 Senter syndrome MalaCards|HPO C4085210 Usual severity pain C0011633 Dermatomyositis HSDN C0751401 Ophthalmoparesis C0026896 Myasthenia gravis OrphaNet|MalaCards C0042798 Vision dim C2931644 O'donnell pappas syndrome MalaCards C0004134 Dyssynergia C0520946 Emotional hypersensitivity HSDN C0034151 Hyperglobulinemic purpura C0030781 Peliosis hepatis HSDN C0242670 Chronic vegetative state C0686721 Babies shaken HSDN C1069915 Vertigo C1548578 Location characteristic id - smoking HSDN C0033377 Caudal displacement C0272309 Simple bruising MalaCards C0000727 Abdomen acute C0004623 Bacterial infections HSDN C3539891 Pelvic pain to the rear C2984289 Melanoma pathway HSDN C2237041 Shox gene with short stature C3554042 Dba11 MalaCards C0042571 Vertigo subjective C0035302 Retinal artery occlusion HSDN C0042928 Paralysis vocal cord C0025064 Mediastinitis HSDN C0751354 Action myoclonus C0751779 Action myoclonus-renal failure syndrome UMLS C0015672 Decreased energy C0017412 Genital diseases, male HSDN C0033377 Caudal displacement C0751885 Myasthenic syndromes, congenital, slow channel MalaCards|HPO C1549543 Administration method - pain C0154778 Myopia, degenerative HSDN C4085548 Usual severity dizziness C0035302 Retinal artery occlusion HSDN C0037763 Spasm C0022104 Irritable bowel syndrome HSDN|UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C1881712 Medical device material rupture HSDN C0042571 Vertigo subjective C0346303 Thyrotroph adenoma MalaCards C0015468 Face pain C3888013 Hypnoses HSDN C0426579 Anorexia symptom C1546533 Specimen source codes - abscess HSDN C0085602 Polydypsia C0027709 Nephrocalcinosis HSDN C0162835 Hypopigmentation C1439329 Cbs gene HPO C0020672 Body temperature decreased C0025286 Meningioma HSDN C2024878 Cardiovascular surgery result: dyspnea C1868703 Bacterial tracheitis HSDN C0042024 Urine incontinence C0025284 Meningeal neoplasms MalaCards C0009806 Constipate C0007138 Carcinoma, transitional cell HSDN C4084768 Usual severity vomiting C1970820 Fabry disease, cardiac variant HPO C2024878 Cardiovascular surgery result: dyspnea C0039614 Tetanus HSDN C2203646 Jaundice C0014849 Esophageal and gastric varices HSDN C0015672 Decreased energy C0033885 Psychoanalytic interpretation HSDN C0036572 Convulsion C4015643 Combined oxidative phosphorylation deficiency 24 MalaCards C0270846 Astatic seizure C2751756 Febrile convulsions, familial, 3a HPO C3539891 Pelvic pain to the rear C0007527 Cecal disease HSDN C4085317 Diarrhea frequency C0085136 Central nervous system neoplasms HSDN C0020903 Illusion C0236969 Substance-related disorders HSDN C0018681 Headache, cephalalgia C0037274 Dermatologic disorders HSDN C1963087 Constipation adverse event C0007784 Cerebral hemisphere hemorrhage HSDN C0424755 Fever symptoms C0023176 Lead poisoning HSDN C0007758 Cerebellar ataxia C0025517 Metabolic diseases HSDN C0242936 Center pain C0016398 Focal infection, dental HSDN C0036396 Sciatica C0860603 Anxiety symptoms HSDN C3898969 Have been vomiting C1833541 Caroli disease isolated MalaCards C0221785 Wrist arthralgia C2702822 Compression arthralgia of left ulna, radius, or wrist UMLS C0518090 Frequency of pain question C0043119 Werner syndrome HSDN C0018965 Blood urine C0268165 Primary hyperoxaluria type 2 MalaCards|HPO C0036572 Convulsion C3806688 Congenital disorder of glycosylation, type iim MalaCards|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0033944 Psychosexual development HSDN C0037763 Spasm C0041327 Tuberculosis, pulmonary HSDN C4085222 Nausea C0393626 Opsoclonus-myoclonus syndrome HSDN C0012833 Dizzy C0010324 Crigler najjar syndrome, type 1 MalaCards C0027498 Nausea vomiting C0747845 Early pregnancy UMLS C0917816 Deficiency mental C0406726 Digito-orofacial syndrome iii MalaCards C0030552 Paralysis partial C0038358 Gastric ulcer HSDN C1279888 Proteinuria of undiagnosed cause C0002985 Angiokeratoma HSDN C4084784 Diarrhea C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C3641755 Have constipation C0006434 Burn injury HSDN C0085636 Light sensitivity C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C1527344 Dysphonia C0004903 Beckwith-wiedemann syndrome HSDN C4084768 Usual severity vomiting C1527336 Sjogren's syndrome HSDN C0030975 Disorders perception C2350521 Gustatory perception HSDN C0036572 Convulsion C0155862 Streptococcal pneumonia HSDN C4084784 Diarrhea C0039082 Syndrome HSDN C0004093 Asthenia C0007528 Cecal neoplasms HSDN C0042963 Symptoms vomiting C3272463 Ampulla of vater undifferentiated carcinoma with osteoclast-like giant cells UMLS C4084768 Usual severity vomiting C1963088 Cystitis adverse event HSDN C0023380 Lethargy C0276357 Swine influenza MalaCards C0016382 Cutaneous vascular engorgement C3280856 Ichthyosis, spastic quadriplegia, and mental retardation MalaCards C0035232 Diaphragmatic paralysis C0238027 Botulism, infantile MalaCards C0007859 Pain neck C0037051 Behavior illness HSDN C4085549 Dizziness C0236736 Cocaine-related disorders HSDN C0020458 Hyperhydrosis C0013364 Dysautonomia, familial OrphaNet|HPO C2984057 Have nausea C0020875 Ileal diseases HSDN C4084802 Usual severity diarrhea C0019294 Hernia, inguinal HSDN C0917816 Deficiency mental C0265251 Oto-palato-digital syndrome type 1 MalaCards C0030552 Paralysis partial C3150933 Hyperaldosteronism, familial, type iii MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0026703 Mucopolysaccharidoses HSDN C0011168 Disorder deglutition C3809824 Parkinson disease 20, early-onset MalaCards C2029884 Hearing loss by exam C0003873 Rheumatoid arthritis HSDN C1549543 Administration method - pain C0039841 Thiamine deficiency HSDN C1971624 Appetite absent C0042961 Intestinal volvulus HSDN C0000727 Abdomen acute C0036341 Schizophrenia HSDN C2237041 Shox gene with short stature C2748918 Otopalatodigital spectrum disorder HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0018128 Graft occlusion, vascular HSDN C0424755 Fever symptoms C0001486 Adenovirus infections HSDN C0010200 Cough symptom C0038661 Suicide HSDN C0006370 Bulimia C2717979 Tooth wear HSDN C0151889 Reflexes tendon increased C3806722 Parkinsonism with spasticity, x-linked MalaCards C0038990 Sweats C0205969 Thymic carcinoma MalaCards C0042798 Vision dim C0042568 Vertebrobasilar insufficiency HSDN C3539020 Pelvic pain decreasing in frequency C0042996 Vulvitis unspecified HSDN C0004134 Dyssynergia C0002871 Anemia HSDN|UMLS C0042798 Vision dim C0023931 Lobstein's disease OrphaNet C2926613 Chest pain:finding:point in time:^patient:ordinal C0549143 Pulmonary renal syndrome MalaCards C0009806 Constipate C0009373 Colonic diseases UMLS C1963281 Vomiting adverse event C1704272 Benign prostatic hyperplasia HSDN C0013421 Dystonia C0002871 Anemia HSDN C0043094 Weight gain C0038002 Splenomegaly HSDN C0015300 Ocular proptosis C0520719 Spinopontine atrophy MalaCards C3829611 Nausea frequency C0038941 Incisional infection HSDN C1963091 Diarrhea adverse event C0029445 Bone necrosis HSDN C0232466 Feeding difficulty C0175691 Dubowitz syndrome MalaCards C0860603 Anxiety symptom C0085547 Phenylketonuria, maternal MalaCards|HPO C0031911 Pigment deposition C0406704 Rudiger syndrome 1 MalaCards C0518090 Frequency of pain question C1000587 Pemphigus HSDN C0036659 Sensation disorder C0019080 Hemorrhage HSDN C2911645 Weight loss adverse event C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C2165518 Depression relieved by good news C0011581 Depressive disorder UMLS C0013362 Dysarthrias C0268514 Urocanase deficiency OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C3714630 Infections, respirovirus HSDN C4085222 Nausea C1963084 Colitis adverse event HSDN C0041657 Consciousness loss C0032787 Postoperative complications HSDN C3887784 Decreased urine output C1566590 Delayed graft function HSDN C0426579 Anorexia symptom C0040948 Trichostrongyliasis HSDN C2936821 Spinal cerebrospinal fluid leak C0521169 Fracture compression HSDN C0004134 Dyssynergia C4082171 Hyperammonemia due to carbamoyl phosphate synthetase 1 deficiency UMLS C0557874 Global developmental delay C3810282 Chromosome 5q12 deletion syndrome MalaCards C0039070 Collapse fleeting C0029456 Osteoporosis HSDN C0262527 Intermittent abdominal pain C0030521 Parathyroid neoplasms MalaCards C0036572 Convulsion C0014548 Epilepsy, generalized UMLS C0086437 Joint hypermobility C1856051 Daish hardman lamont syndrome MalaCards C0020649 Blood pressure decreased C0270726 Alexander disease OrphaNet|MalaCards C3887873 Hearing loss C4084909 Depression subordinate domain HSDN C4085210 Usual severity pain C0025268 Multiple endocrine neoplasia type 2a HSDN C1963167 Memory impairment adverse event C2931082 Familial apoceruloplasmin deficiency MalaCards C0033377 Caudal displacement C0022541 Kearns-sayre syndrome MalaCards C0016199 Pain flank C0001422 Adenofibroma HSDN C0012833 Dizzy C0206255 Malaria vaccine HSDN C2237041 Shox gene with short stature C2931302 Familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails OrphaNet|MalaCards C0522224 Palsied C0014394 Enuresis HSDN C2024878 Cardiovascular surgery result: dyspnea C0038436 Post-traumatic stress disorder HSDN C0349588 Stature short C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C3463815 Feel fatigue C1334928 Necrotic changes (finding) HSDN C0007758 Cerebellar ataxia C0017178 Gastrointestinal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162834 Hyperpigmentation HSDN C3463815 Feel fatigue C2931916 Midline granulomatosis MalaCards C4084724 Usual severity constipation C0009241 Cognition disorders HSDN C0026838 Spasticity muscle C2931845 Neurodegeneration with brain iron accumulation (nbia) OrphaNet|MalaCards C3146279 Coma C0019080 Hemorrhage HSDN C1549543 Administration method - pain C0026272 Mixed connective tissue disease HSDN C0027497 Queasy C0428977 Bradycardia HSDN C3665492 Pigmentations C1956257 Pulmonary stenosis MalaCards C0042963 Symptoms vomiting C1879737 Aromatherapy and essential oils HSDN C0042798 Vision dim C0206255 Malaria vaccine HSDN C0039070 Collapse fleeting C1384672 Hpt gene HSDN C2911645 Weight loss adverse event C0041374 Tumor virus infections HSDN C0036572 Convulsion C0034345 Pyruvate dehydrogenase complex deficiency disease OrphaNet|HPO|MalaCards C1971624 Appetite absent C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0034124 Pupillary disorder C0007761 Myoclonic cerebellar dyssynergia HSDN C0005745 Blepharoptosis C0751267 Encephalopathy, subacute necrotizing, infantile MalaCards C0013404 Respiratory difficulty C0524851 Neurodegenerative disorders HSDN C1961100 Erectile dysfunction adverse event C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C0521635 Female genital leucoplakia C0269194 Cervical leukoplakia UMLS C2237041 Shox gene with short stature C1833603 Spondyloepiphyseal dysplasia with atlantoaxial instability MalaCards C0030554 Abnormal sensation C0020598 Hypocalcemia HSDN C0030232 Color loss C0039131 Syphilis congenital HSDN C2919142 Short stature adverse event C1856738 Fibular hypoplasia and complex brachydactyly OrphaNet|HPO C0000737 Abdomen pain C0037313 Sleep HSDN C4084802 Usual severity diarrhea C0042384 Vasculitis HSDN C1384666 Decreased hearing C0043251 Wounds and injuries HSDN C0424755 Fever symptoms C1527336 Sjogren's syndrome HSDN C0151908 Dry skin C0852007 Scleroderma and associated disorders OrphaNet C0030975 Disorders perception C0011884 Diabetic retinopathy HSDN C0018681 Headache, cephalalgia C1962986 Glaucoma adverse event HSDN C0043094 Weight gain C0080179 Vertebra fracture HSDN C2242996 Tingling C0023786 Mucopolysaccharidosis i OrphaNet C0000737 Abdomen pain C0018799 Heart diseases HSDN C0013421 Dystonia C0025427 Mercury poisoning OrphaNet|MalaCards C0019079 Bloody sputum C0040588 Tracheoesophageal fistula HSDN C0518090 Frequency of pain question C0042133 Uterine fibroids HSDN C0042963 Symptoms vomiting C0178282 Hernia of abdominal cavity HSDN C0206146 Myocardial stunning C0085298 Sudden cardiac death HSDN C3274924 Have been coughing C0042029 Urinary tract infection HSDN C1557397 Adverse event associated with pain C0013364 Dysautonomia, familial HSDN C1557397 Adverse event associated with pain C0027707 Nephritis, interstitial HSDN C0020903 Illusion C0042812 Acuity visual HSDN C0013362 Dysarthrias C2677567 Dystonia 16 (disorder) MalaCards|HPO C4084776 Weight loss C0566602 Primary sclerosing cholangitis OrphaNet|HPO|MalaCards C0009421 Comatose C0162871 Aortic aneurysm, abdominal HSDN C4084724 Usual severity constipation C0006057 Botulisms OrphaNet|MalaCards C0003550 Broca aphasia C3810814 Myocardial infarction ecg assessment HSDN C0028738 Nystagmus C0206307 Canavan disease MalaCards|HPO C0728710 Pupil constriction observed C0752347 Lewy body disease HSDN C0017181 Gastrointestinal bleed C0086922 Purpura rheumatoid MalaCards C0018784 Deafness sensorineural C3495801 Granulomatosis with polyangiitis MalaCards|HPO C0020455 Hypergammaglobulinemia C0019159 Hepatitis a HSDN C0026603 Motion sickness C0004936 Mental disorders HSDN C0015970 Fever unknown origin C0035243 Respiratory tract infections HSDN C2919142 Short stature adverse event C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C0019209 Large liver C0085655 Polymyositis MalaCards C0014591 Bleeding nose C3888026 Hermansky-pudlak syndrome 8 MalaCards C1549543 Administration method - pain C0085084 Motor neuron disease HSDN C4084784 Diarrhea C0020507 Hyperplasia HSDN C0030193 Sense of pain C0151491 Congenital musculoskeletal anomalies HSDN C0018965 Blood urine C0036421 Systemic scleroderma MalaCards C0042024 Urine incontinence C2706915 Language:-:point in time:^patient:- HSDN C0031911 Pigment deposition C1332614 Angiosarcoma of the breast MalaCards C4085548 Usual severity dizziness C0001580 Adolescent behavior HSDN C2024878 Cardiovascular surgery result: dyspnea C1260409 Myasthenia gravis without acute exacerbation MalaCards C0018772 Deafness C0013261 Duane retraction syndrome HSDN C3815497 Cough C3540844 Ciliary dyskinesia, primary, 20 MalaCards C0007758 Cerebellar ataxia C2752074 Alpha-ketoglutarate dehydrogenase deficiency OrphaNet|HPO|MalaCards C4085661 Usual severity nausea C0007222 Cardiovascular diseases HSDN C0005874 Blush C0473546 Vibratory angio-edema MalaCards C0040264 Ear ringing sound C0270617 Adhesive arachnoiditis OrphaNet|MalaCards C1557397 Adverse event associated with pain C0032290 Aspiration pneumonia HSDN C0151786 Weakness muscle C0039516 Tennis elbow HSDN C4084769 Vomiting frequency C0428977 Bradycardia HSDN C4084776 Weight loss C0027625 Circulating neoplastic cells HSDN C0233565 Bradykinesia C3554079 Combined oxidative phosphorylation deficiency 12 MalaCards C3815497 Cough C0025284 Meningeal neoplasms HSDN C0917816 Deficiency mental C1846055 Siderius x-linked mental retardation syndrome MalaCards|HPO C0723402 Sore throat C0023092 Lassa fever MalaCards C4085210 Usual severity pain C0011606 Exfoliative dermatitis HSDN C0242936 Center pain C0015923 Fetal alcohol syndrome HSDN C0241165 Skin thickening C2931506 Stern lubinsky durrie syndrome MalaCards C0018784 Deafness sensorineural C1859133 Rhizomelic chondrodysplasia punctata, type 1 HPO C0242936 Center pain C1541646 Spirituality therapy HSDN C0026821 Cramp C0152025 Polyneuropathy HSDN C4084767 Bothered by vomiting C0243025 Hantavirus pulmonary syndrome MalaCards C3812171 Bradycardia by ecg finding C1970298 Progressive familial heart block, type ib MalaCards|HPO C0038002 Spleen enlargement C0009714 Hepatic fibrosis, congenital HPO C2911645 Weight loss adverse event C1552527 Clinic / center - developmental disabilities HSDN C0040485 Wryneck C0042138 Uterine neoplasms HSDN C0042798 Vision dim C3178817 Paraneoplastic syndromes, ocular HSDN C0002962 Angina C0006277 Bronchitis HSDN C4085222 Nausea C0031039 Effusion pericardial HSDN C0853986 Lymphocytes decreased C1858664 Hemochromatosis, type 3 MalaCards C4085661 Usual severity nausea C0023474 Leukemia, myeloid, chronic-phase HSDN C0013395 Indigestion C0042029 Urinary tract infection HSDN C3641756 Have diarrhea C0025534 Metal metabolism, inborn errors HSDN C0015672 Decreased energy C0040425 Tonsillitis HSDN C2024893 Cardiovascular surgery result: fatigue C0021933 Intussusception HSDN C0349588 Stature short C1833380 Velofacioskeletal syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0016563 Form perception HSDN C1549543 Administration method - pain C0018965 Hematuria HSDN C0518090 Frequency of pain question C0023269 Leiomyosarcoma HSDN C3641756 Have diarrhea C0043046 Wasting syndrome HSDN C0040822 D tremors C0013295 Duodenal ulcer HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0752155 Central nervous system vascular malformations HSDN C1384666 Decreased hearing C1838329 Aplasia cutis congenita with epibulbar dermoids MalaCards C1963184 Nystagmus adverse event C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C4084727 Cough frequency C0018802 Congestive heart failure HSDN C1557397 Adverse event associated with pain C0020120 Engineering humans HSDN C4084774 Have weight loss C0852007 Scleroderma and associated disorders OrphaNet C3463815 Feel fatigue C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C0728710 Pupil constriction observed C0003534 Aphakia HSDN C1145670 Failure respiratory C1968556 Encephalopathy, neonatal severe, due to mecp2 mutations HPO C0002963 Angina variant C1963138 Hypertension adverse event HSDN C0856180 Retracted nipple (excl lactation) C0221370 Nipple retracted UMLS C0240715 Perineal lump C1290302 Neoplasm of muscle of perineum UMLS C0030975 Disorders perception C0004377 Automatism HSDN C2984058 Have pain C0023869 Lithiasis HSDN C0015672 Decreased energy C0033348 Language program HSDN C0700078 Deep tendon reflex decrease C0751276 Metachromatic leukodystrophy, juvenile type HPO C1963137 Hydrocephalus adverse event C1707400 Classic medulloblastoma MalaCards C0003467 Angst C3810225 Mental retardation, autosomal recessive 41 MalaCards C0024312 Lymphocytopenia C0265354 Charge syndrome MalaCards|HPO C4085211 Pain distress question C0027022 Myeloproliferative disease HSDN C0042571 Vertigo subjective C0036341 Schizophrenia HSDN C1963281 Vomiting adverse event C0016057 Fibrosarcoma HSDN C0025323 Bleeding menstrual heavy C0015523 Factor xi deficiency OrphaNet C1963252 Tremor adverse event C0020550 Hyperthyroidism HSDN C3665347 Vision impaired C3150715 Retinitis pigmentosa 51 MalaCards|HPO C0242936 Center pain C0004509 Azoospermia HSDN C0727671 Red cross toothache drops C1999266 Depression adverse event HSDN C0026838 Spasticity muscle C0041330 Tuberculosis, spinal HSDN C4084769 Vomiting frequency C0025061 Disease of mediastinum HSDN C2911645 Weight loss adverse event C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C1557397 Adverse event associated with pain C0020627 Hypopharyngeal neoplasms HSDN C3146279 Coma C0039082 Syndrome HSDN C0013604 Edematous C0006264 Bronchial neoplasms HSDN C0851578 Disorder sleep C0919267 Ovarian neoplasm HSDN C0700078 Deep tendon reflex decrease C1854150 Charcot-marie-tooth disease, type 2b2 HPO C1963063 Anorexia adverse event C0023281 Leishmaniasis MalaCards C0005779 Clotting C0022739 Klippel-trenaunay-weber syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0015397 Disorder of eye HSDN C2911647 Weight gain adverse event C0011389 Dental plaque HSDN C4085549 Dizziness C0012979 Canine disease HSDN C0917816 Deficiency mental C1969053 Joubert syndrome 7 MalaCards|HPO C0011991 Loose stools C0018099 Gout HSDN C2911645 Weight loss adverse event C0010340 Critical illness HSDN C0042963 Symptoms vomiting C0270639 Lateral sinus thrombosis HSDN C3274924 Have been coughing C0398370 Lipedema HSDN C0518090 Frequency of pain question C0004898 Beauties HSDN C1549543 Administration method - pain C0029882 Otitis media HSDN C1963091 Diarrhea adverse event C0027670 Neoplastic endocrine-like syndromes HSDN C0020505 Excessive eating C0236642 Pick disease of the brain HPO C0000731 Abdomen distention C1401162 Carbohydrate intolerance MalaCards C0018772 Deafness C0029139 Optical illusion HSDN C0030193 Sense of pain C0036472 Scrub typhus HSDN C0013404 Respiratory difficulty C0314657 Genetic predisposition HSDN C2911647 Weight gain adverse event C0042485 Venous insufficiency HSDN C0027796 Neuralgias C0004352 Autistic disorder HSDN C4084802 Usual severity diarrhea C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C0858557 Lip redness C0007971 Cheilitis UMLS C1963071 Back pain adverse event C0021364 Male infertility HSDN C0027796 Neuralgias C1963067 Atrial fibrillation adverse event HSDN C0030552 Paralysis partial C0037952 Spinocerebellar degeneration HSDN C4042891 Sleep wake disorders C0026948 Mycosis fungoides HSDN C2237041 Shox gene with short stature C0265961 Erythrokeratodermia variabilis OrphaNet|HPO C0151889 Reflexes tendon increased C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0010200 Cough symptom C0002874 Aplastic anemia HSDN C4084766 Vomiting C2748608 Lead poisoning, susceptibility to HPO C3887638 Failure to thrive in infant C1510455 Acrocephalosyndactylia HSDN C0349588 Stature short C2677299 Cerebroretinal microangiopathy with calcifications and cysts (disorder) HPO C0240735 Personality change C1862937 Ftdals1 HPO C1963249 Tinnitus adverse event C0003469 Anxiety disorders HSDN C0015469 Facial paralysis C0007130 Mucinous adenocarcinoma HSDN C0036572 Convulsion C0037322 Active eye movement sleep HSDN C0494475 Seizure generalized tonic clonic C1833104 Diabetes mellitus, permanent neonatal OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0020179 Huntington disease HSDN C0426579 Anorexia symptom C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0234132 Pyramidal sign C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|UMLS C0007815 Cerebrospinal fluid rhinorrhoea C0027429 Nasal obstruction present finding HSDN C0043094 Weight gain C0020517 Hypersensitivity HSDN C4084726 Distress cough C0004610 Bacteremia HSDN C0026826 High muscle tone C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0162834 Hyperpigmentation C3151055 Adrenal insufficiency, congenital, with 46,xy sex reversal, partial or complete HPO C2984058 Have pain C0034088 Pulmonary valve insufficiency HSDN C4084767 Bothered by vomiting C0019348 Herpes simplex infections HSDN C1963281 Vomiting adverse event C0016563 Form perception HSDN C0033774 Skin pruritus C0025063 Mediastinal neoplasms HSDN C1961131 Cough adverse event C2937421 Prostatic hyperplasia HSDN C0009080 Finger clubbing C1868081 Juvenile polyposis coli HPO C0003467 Angst C1853445 Parkinson disease 7, autosomal recessive early-onset MalaCards|HPO C3887638 Failure to thrive in infant C1839530 Valproate sensitivity HPO C2919142 Short stature adverse event C0265251 Oto-palato-digital syndrome type 1 MalaCards C0040822 D tremors C0032858 Powassan encephalitis MalaCards C2919142 Short stature adverse event C0398791 Nijmegen breakage syndrome OrphaNet|HPO|MalaCards C0019572 Hairiness C3275471 Mental retardation, x-linked, syndromic, chudley-schwartz type MalaCards C3463815 Feel fatigue C1833518 Carnitine palmitoyltransferase ii deficiency, lethal neonatal OrphaNet|HPO C0036572 Convulsion C1332202 Adult ganglioglioma UMLS C0518090 Frequency of pain question C0027022 Myeloproliferative disease HSDN C0030193 Sense of pain C1963266 Uveitis adverse event HSDN C0271215 Blindness legal C1968804 Plasminogen deficiency, type i MalaCards|HPO C0917816 Deficiency mental C0033835 Pseudopseudohypoparathyroidism MalaCards|HPO C4085222 Nausea C0016751 Hereditary fructose intolerance syndrome HPO C0036572 Convulsion C0041408 Turner syndrome HSDN C2024893 Cardiovascular surgery result: fatigue C0042133 Uterine fibroids HSDN C0007758 Cerebellar ataxia C0812437 Oculo-dento-digital syndrome OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0023860 Listeriosis HSDN C0015468 Face pain C1263846 Attention deficit hyperactivity disorder HSDN C0010200 Cough symptom C0035412 Rhabdomyosarcoma HSDN C0018808 Murmur C0018802 Congestive heart failure HSDN C0557874 Global developmental delay C0265493 Cat eye syndrome MalaCards C0013362 Dysarthrias C2680446 Spastic paraplegia 43, autosomal recessive MalaCards C0241157 Skin pustule C0398367 Histiocytic necrotizing lymphadenitis MalaCards C2237041 Shox gene with short stature C1833454 Komuragaeri disease OrphaNet|MalaCards C0850758 Pain pelvic C0272414 Displaced spleen HSDN C0231712 Gait waddling C0751337 X-linked emery-dreifuss muscular dystrophy MalaCards|HPO|UMLS C1963281 Vomiting adverse event C0238154 Epidural hematoma HSDN C3641756 Have diarrhea C0014474 Ependymoma HSDN C0007758 Cerebellar ataxia C0038454 Cerebrovascular accident HSDN C0018989 Paresis of one side of body C0000768 Congenital abnormality UMLS C0085593 Chill C0812413 Malignant pleural mesothelioma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0020621 Hypokalemia HSDN C4084775 Usual severity weight loss C0018916 Hemangioma HSDN C0522224 Palsied C0037744 Perceptual spatial orientation HSDN C0241538 Upper extremity numbness C0745881 Lower extremity paresthesia tingling UMLS C0035229 Respiratory function impaired C0393814 Hereditary liability to pressure palsies HPO C0010520 Skin cyanosis C0002871 Anemia HSDN C0040822 D tremors C1546847 Entity name part type - family HSDN C0423714 Genitofemoral nerve neuralgia C0574718 Lower limb nerve lesion UMLS C0009806 Constipate C0037997 Splenic diseases HSDN C0036572 Convulsion C3266101 22q11 partial monosomy syndrome HPO C0009806 Constipate C0009244 Behavioral cognitive therapy HSDN C0026821 Cramp C0019112 Hemorrhoids HSDN C4084776 Weight loss C1555914 Psychologist - psychotherapy, group HSDN C0040485 Wryneck C0041330 Tuberculosis, spinal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1704436 Peripheral arterial diseases HSDN C2984058 Have pain C0013928 Fat embolism HSDN C0030200 Intractable pain C0002940 Aneurysm HSDN C4084788 Have dizziness C1090821 Sepsis (invertebrate) HSDN C0030554 Abnormal sensation C1458155 Mammary neoplasms HSDN C4084766 Vomiting C0398623 Thrombophilia HSDN C3665347 Vision impaired C0265313 Weill-marchesani syndrome MalaCards|HPO C0034933 Abnormal reflexes C0030920 Peptic ulcer HSDN C0857305 Thrombocytopenia purpura C0030781 Peliosis hepatis HSDN C4084773 Bothered by weight gain C0013418 Abnormal labor HSDN C4084724 Usual severity constipation C0021051 Immunologic deficiency syndromes HSDN C3146279 Coma C2931918 Transketolase defect MalaCards C0028738 Nystagmus C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C4084775 Usual severity weight loss C0027743 Nerve compression syndrome HSDN C0024031 Back pain lower back C0021831 Intestinal diseases HSDN C3146279 Coma C2931788 Atypical hemolytic uremic syndrome MalaCards C1963064 Anxiety adverse event C0342443 Adrenal cushing's syndrome MalaCards C0002962 Angina C0037928 Spinal cord diseases HSDN C3203358 Alveolar hypoventilation C0016196 Chest flail HSDN C1963281 Vomiting adverse event C0268328 Porphobilinogen synthase deficiency MalaCards|HPO C0030193 Sense of pain C0040443 Avulsed tooth HSDN C4085210 Usual severity pain C0151740 Intracranial hypertension HSDN C0030975 Disorders perception C1510539 Emotional intelligence HSDN C0005779 Clotting C0042974 Von willebrand disease OrphaNet|MalaCards C3898969 Have been vomiting C0268193 Nadh cytochrome b5 reductase deficiency MalaCards|HPO C0004134 Dyssynergia C0034345 Pyruvate dehydrogenase complex deficiency disease OrphaNet|MalaCards C4084776 Weight loss C0004031 Aspergillosis, allergic bronchopulmonary OrphaNet|MalaCards C1963065 Apnea adverse event C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0162739 Hellp syndrome HSDN C0231749 Knee arthralgia C2675767 Edm6 MalaCards C0030552 Paralysis partial C0001231 Acth syndrome, ectopic MalaCards C4084727 Cough frequency C0027889 Hereditary sensory and autonomic neuropathies HSDN C1557397 Adverse event associated with pain C0870082 Hyperkeratosis HSDN C1384666 Decreased hearing C3179239 Osteopetrosis autosomal dominant type 2 MalaCards|HPO C1963170 Hypothermia adverse event C0022650 Kidney calculi HSDN C0013404 Respiratory difficulty C1962971 Myocarditis adverse event HSDN C4085862 Bothered by nausea C3495422 Finding relating to sexuality and sexual activity HSDN C3815497 Cough C0342443 Adrenal cushing's syndrome HSDN C4085210 Usual severity pain C2219717 Menstrual periods stopped for over 6 months HSDN C0009421 Comatose C0006105 Brain abscess HSDN C1549543 Administration method - pain C0032326 Pneumothorax HSDN C0013421 Dystonia C0011853 Diabetes mellitus, experimental HSDN C0023885 Liver abscess C0279607 Adult primary hepatocellular carcinoma MalaCards C0013404 Respiratory difficulty C1708781 Lung sarcomatoid carcinoma UMLS C0008031 Pain chest C0037939 Spinal neoplasms HSDN C0018989 Paresis of one side of body C0268328 Porphobilinogen synthase deficiency MalaCards C0033774 Skin pruritus C1318558 Congenital melanocytic nevus HPO C0030552 Paralysis partial C0023529 Leukomalacia, periventricular HSDN C4085317 Diarrhea frequency C0020877 Ileitis DiseaseOntology|MalaCards C0039070 Collapse fleeting C0031090 Periodontal diseases HSDN C4084773 Bothered by weight gain C0023890 Liver cirrhosis HSDN C0011991 Loose stools C0040435 Tooth diseases HSDN C3539891 Pelvic pain to the rear C0009244 Behavioral cognitive therapy HSDN C1971624 Appetite absent C0024121 Lung neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0752308 Hypoxia-ischemia, brain HSDN C4084802 Usual severity diarrhea C0007527 Cecal disease HSDN C0012833 Dizzy C0039614 Tetanus HSDN C4084767 Bothered by vomiting C0024143 Lupus nephritis HSDN C3887638 Failure to thrive in infant C0796033 Marden-walker syndrome MalaCards C0042928 Paralysis vocal cord C0520946 Emotional hypersensitivity HSDN C0231528 Muscle pain generalized C0017589 Farcy DiseaseOntology|MalaCards C3539889 Pelvic pain increasing in severity C0037369 Smoking HSDN C0018775 Hearing loss bilateral C0162666 Mitochondrial encephalomyopathies HSDN C0030193 Sense of pain C0024862 Masochism HSDN C0000737 Abdomen pain C0043195 Subsepsis hyperergia syndrome OrphaNet|MalaCards C3274924 Have been coughing C0041296 Tuberculosis OrphaNet|HPO C0522224 Palsied C0006434 Burn injury HSDN C1549543 Administration method - pain C0040196 Tick infestations HSDN C1961131 Cough adverse event C0517555 Venous thrombosis after immobility HSDN C4084723 Constipation C0043352 Xerostomia HSDN C0020455 Hypergammaglobulinemia C0019087 Hemorrhagic disorders HSDN C0917816 Deficiency mental C1412746 Bbs1 gene HPO C0011991 Loose stools C0008533 Hemophilia b HSDN C0232466 Feeding difficulty C3151097 Meier-gorlin syndrome 2 MalaCards|HPO C4084775 Usual severity weight loss C0878684 Short syndrome MalaCards C0020903 Illusion C0600091 Identifiers HSDN C1384666 Decreased hearing C1852759 Papillorenal syndrome MalaCards|HPO C0042025 Urinary incontinence stress C0000735 Abdominal neoplasms HSDN C0000737 Abdomen pain C0020456 Hyperglycemia HSDN C0036572 Convulsion C0221056 Adult type dermatomyositis HSDN C0036572 Convulsion C3281138 Chromosome 17q12 deletion syndrome MalaCards C4084802 Usual severity diarrhea C0029182 Orbit (eye disorders) HSDN C1557397 Adverse event associated with pain C0521585 Gastrointestinal mucositis HSDN C0242936 Center pain C0024638 Class ii division 2 malocclusion HSDN C3887638 Failure to thrive in infant C2931189 Neural crest tumor MalaCards C0030552 Paralysis partial C0001721 Emotional affect HSDN C0030193 Sense of pain C0039786 Therapeutic communities HSDN C0009806 Constipate C2983137 Colon carcinoma metastatic in the lung UMLS C1557397 Adverse event associated with pain C0011405 Pulp disorder HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1546847 Entity name part type - family HSDN C0005745 Blepharoptosis C0041408 Turner syndrome MalaCards C3274924 Have been coughing C0038325 Stevens-johnson syndrome HPO C2203646 Jaundice C0027627 Neoplasm metastasis HSDN C0015468 Face pain C0344434 Atrial fibrillation ecg HSDN C0002170 Alopecia disorders C1855607 Keutel syndrome MalaCards|HPO C3274924 Have been coughing C0020676 Hypothyroidism HSDN C4084776 Weight loss C0017658 Glomerulonephritis HSDN C0037771 Paraparesis spastic C0017495 Gerstmann-straussler-scheinker disease HSDN C0036572 Convulsion C2219717 Menstrual periods stopped for over 6 months HSDN C0018932 Bright red rectal bleeding C0039445 Hereditary hemorrhagic telangiectasia HPO C2984057 Have nausea C0018188 Granuloma HSDN C0034150 Skin purpura C1961100 Erectile dysfunction adverse event HSDN C0013404 Respiratory difficulty C0040185 Tibia fracture HSDN C0162285 Edema eyelid C0023092 Lassa fever OrphaNet|MalaCards C4084725 Usual severity cough C0006845 Candidiasis, chronic mucocutaneous MalaCards|HPO C0016199 Pain flank C0043254 Injuries penetrating HSDN C0009421 Comatose C0032269 Pneumococcal infections HSDN C0085632 Listlessness C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards|UMLS C0018777 Deafness, conductive C0334419 Pheochromocytoma, malignant MalaCards C4085211 Pain distress question C0220981 Metabolic acidosis HSDN C0034150 Skin purpura C0997768 Glaucoma HSDN C0011991 Loose stools C0026946 Mycoses HSDN C1557397 Adverse event associated with pain C0027868 Neuromuscular diseases HSDN C1961131 Cough adverse event C0263666 Dermatomyositis, childhood type MalaCards C0023012 Delay language C3150941 Rubinstein-taybi syndrome 2 MalaCards|HPO C1963252 Tremor adverse event C0022802 Kuru HSDN C4085211 Pain distress question C0035317 Retinal hemorrhage HSDN C4084775 Usual severity weight loss C0011253 Delusions HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003892 Neurogenic arthropathy HSDN C3541349 Syncope C0039263 Takayasu arteritis HSDN C0332563 Papulae C0268140 Xeroderma pigmentosum, group f HPO C0030552 Paralysis partial C1261470 Congenital meningocele HSDN C0476273 Distress respiratory C1535917 Nipah virus infection MalaCards C0019079 Bloody sputum C1708776 Mucinous adenocarcinoma of lung UMLS C2984058 Have pain C0017152 Gastritis HSDN C0150055 Pain chronic C0080040 Polio post syndrome HSDN C0424755 Fever symptoms C0019202 Hepatolenticular degeneration HSDN C0020673 Hypothermia (central) (local) C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0151827 Pain eye C2237660 Exudative macular degeneration HSDN C4085210 Usual severity pain C0008372 Intrahepatic cholestasis HSDN C4084768 Usual severity vomiting C0022665 Kidney neoplasm HSDN C0007758 Cerebellar ataxia C2749485 Nblst1 HPO C3539889 Pelvic pain increasing in severity C0007097 Carcinomas HSDN C0454644 Delayed language development C1865644 Plantar lipomatosis, unusual facies, and developmental delay MalaCards|HPO C0020673 Hypothermia (central) (local) C1261473 Sarcoma HSDN C0040259 Tinea pedis C0029411 Osteoarthropathy, primary hypertrophic HSDN C2919142 Short stature adverse event C1527404 Female pseudo-turner syndrome HPO C0017181 Gastrointestinal bleed C1835664 Tylosis with esophageal cancer MalaCards C3641755 Have constipation C1837218 Cleft palate, isolated HSDN C0034933 Abnormal reflexes C0036690 Septicemia HSDN C0042024 Urine incontinence C1565489 Renal insufficiency HSDN C1962972 Proteinuria adverse event C0039082 Syndrome HSDN C0026838 Spasticity muscle C3151619 Ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation UMLS C3665492 Pigmentations C1334625 Malignant non-seminomatous germ cell cancer of testis MalaCards C0005745 Blepharoptosis C0006057 Botulisms MalaCards C0040822 D tremors C0020542 Pulmonary hypertension HSDN C4084768 Usual severity vomiting C0026598 Movement perception HSDN C1962972 Proteinuria adverse event C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0040034 Thrombocytopenia C1959626 Mevalonic aciduria MalaCards|HPO C0030193 Sense of pain C0030849 Penile neoplasms HSDN C0033774 Skin pruritus C0600336 Subcorneal pustular dermatosis OrphaNet|MalaCards C3539890 Pelvic pain causes awakening at night C1394494 Cystocele, unspecified HSDN C0030486 Extremity paralysis, lower C0008370 Cholestasis HSDN C0008031 Pain chest C0729233 Dissecting aneurysm of the thoracic aorta UMLS C0039070 Collapse fleeting C0038160 Staphylococcal infections HSDN C0019079 Bloody sputum C0038463 Strongyloides infection HSDN C4085317 Diarrhea frequency C0020459 Hyperinsulinism HSDN C2024893 Cardiovascular surgery result: fatigue C0043168 Whooping cough due to unspecified organism HSDN C0028738 Nystagmus C0220767 Craniofrontonasal dysplasia HPO C3641756 Have diarrhea C0000833 Abscess HSDN C4085862 Bothered by nausea C0001883 Airway obstruction HSDN C0020673 Hypothermia (central) (local) C0006118 Brain neoplasms HSDN C0426579 Anorexia symptom C0022660 Kidney failure, acute HSDN C4084774 Have weight loss C0031485 Phenylketonurias HSDN C1963281 Vomiting adverse event C0268647 Lysinuric protein intolerance MalaCards|HPO C4084802 Usual severity diarrhea C3495801 Granulomatosis with polyangiitis HSDN C1963091 Diarrhea adverse event C0008065 Childhood behavior HSDN C3274924 Have been coughing C0011981 Diaphragmatic eventration HSDN C1549543 Administration method - pain C3469521 Fanconi anemia, complementation group a (disorder) HSDN C0003862 Pain joint C0024121 Lung neoplasms HSDN C4084773 Bothered by weight gain C0001726 Affective symptoms HSDN C4084723 Constipation C0018801 Heart failure HSDN C0022638 Ketosis C0342749 Glycogen storage disease ic MalaCards|HPO C0043094 Weight gain C0439840 Reflex motion descriptor HSDN C2984058 Have pain C0679360 Foodborne disease HSDN C1838869 Proximal neurogenic muscle weakness C1969785 Muscular dystrophy, limb-girdle, type 2l (disorder) MalaCards|HPO C4084774 Have weight loss C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C0020649 Blood pressure decreased C1335686 Neuroendocrine neoplasm of rectum MalaCards C3494358 Characteristic, prodromal C0001442 Adenosarcoma HSDN C0518090 Frequency of pain question C0868910 Oligozoospermia HSDN C2025995 Cellulitis C0023241 Legionnaires' disease MalaCards C1253937 Pericardial effusion C0085404 Poems syndrome MalaCards C0041657 Consciousness loss C0027765 Nervous system disorder HSDN C0028738 Nystagmus C1854990 Molybdenum cofactor deficiency, complementation group c HPO C2984058 Have pain C0751922 Median neuropathy HSDN C0010038 Corneal opacity disorder C1838348 Oculomaxillofacial dysostosis OrphaNet|MalaCards C3539892 Pelvic pain in front C2586211 Thrombosis of blood vessel HSDN C0030200 Intractable pain C0005491 Biofeedback HSDN C0027498 Nausea vomiting C0001339 Acute pancreatitis UMLS C3815497 Cough C0016548 Foreign body migration HSDN C0003811 Cardiac rhythm disturbance C0410190 Autosomal dominant emery-dreifuss muscular dystrophy (disorder) HPO C4084774 Have weight loss C0026650 Movement disorders HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0013295 Duodenal ulcer HSDN C0041657 Consciousness loss C0007772 Intracranial arteriovenous malformation HSDN C4084724 Usual severity constipation C0002395 Alzheimer's disease HSDN C0018772 Deafness C0265301 Sclerosteosis HPO C0022346 Yellow skin C0017563 Gingival diseases HSDN C2242996 Tingling C0011849 Diabetes mellitus HSDN C3665347 Vision impaired C0033788 Pseudo-hurler polydystrophy OrphaNet|MalaCards C2315100 Pediatric failure to thrive C1858328 Bile acid synthesis defect, congenital, 4 MalaCards|HPO C4084766 Vomiting C0007193 Cardiomyopathy, dilated HSDN C0011570 Monopolar depression C0271865 Autoimmune hypoparathyroidism MalaCards C4084788 Have dizziness C0340493 Paroxysmal familial ventricular fibrillation MalaCards C4084726 Distress cough C0034063 Pulmonary edema HSDN C3829611 Nausea frequency C0021847 Intestinal pseudo-obstruction HSDN C0020578 Hyperventilate C0022660 Kidney failure, acute HSDN C0424755 Fever symptoms C0080179 Vertebra fracture HSDN C0221263 Cafe au lait spot C0027809 Neurilemmoma HSDN C2911647 Weight gain adverse event C0023798 Lipoma HSDN C0518090 Frequency of pain question C0017570 Gingival neoplasms HSDN C4085317 Diarrhea frequency C0005283 Beta thalassemia HSDN C0018772 Deafness C1838099 Abcd syndrome MalaCards|HPO C0019825 Voice hoarseness C0205770 Choroid plexus papilloma HSDN C4084776 Weight loss C0006105 Brain abscess HSDN C3274924 Have been coughing C0019348 Herpes simplex infections HSDN C0018775 Hearing loss bilateral C0007873 Uterine cervical neoplasm HSDN C0040822 D tremors C0013080 Down syndrome HSDN C2024878 Cardiovascular surgery result: dyspnea C0018196 Granuloma of larynx HSDN C0232466 Feeding difficulty C1853566 Genitopatellar syndrome MalaCards|HPO C3539890 Pelvic pain causes awakening at night C0008519 Ectopic tissue HSDN C1384666 Decreased hearing C3810170 Deafness, autosomal dominant 56 MalaCards C0030552 Paralysis partial C0021308 Infarction HSDN C0015672 Decreased energy C0021799 Interprofessional relations HSDN C0023380 Lethargy C0022521 Kartagener syndrome HSDN C0009806 Constipate C0018099 Gout HSDN C0013404 Respiratory difficulty C0027439 Nasopharyngeal neoplasms HSDN C4084788 Have dizziness C0043251 Wounds and injuries HSDN C1557397 Adverse event associated with pain C0006430 Burning mouth syndrome HSDN C4084768 Usual severity vomiting C0005974 Bone resorption HSDN C0013456 Pain ear C3178777 Bisphosphonate associated osteonecrosis of the jaw HSDN C2032396 Pelvic pain on the right C1299262 Sarcoma - category (morphologic abnormality) HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0012817 Diverticulum HSDN C1557397 Adverse event associated with pain C0035228 Respiratory hypersensitivity HSDN C3898969 Have been vomiting C0282207 Cronkhite-canada syndrome MalaCards C1962957 Flushing adverse event C0406810 Carney complex HSDN C4084784 Diarrhea C0008626 Congenital chromosomal disease HSDN C0002962 Angina C3812171 Bradycardia by ecg finding HSDN C0030486 Extremity paralysis, lower C2931642 Benign symmetrical lipomatosis HSDN C4084724 Usual severity constipation C0268322 Chester-type porphyria HPO C0011991 Loose stools C0018051 Gonadal dysgenesis HSDN C1971624 Appetite absent C1334374 Laryngeal neuroendocrine neoplasm MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0009442 Common bile duct neoplasms HSDN C4084769 Vomiting frequency C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C3541349 Syncope C0007282 Carotid stenosis HSDN C0011991 Loose stools C3150354 Immunodeficiency, common variable, 2 MalaCards|HPO|UMLS C0013604 Edematous C1527298 Dysentery, bacillary HSDN C1963091 Diarrhea adverse event C0836924 Thrombocytosis HSDN C4085642 Level of joint stiffness C0175702 Williams syndrome OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C4045991 Perihilar cholangiocarcinoma MalaCards C0013604 Edematous C0027809 Neurilemmoma HSDN C0040485 Wryneck C0027095 Myosarcoma HSDN C4085548 Usual severity dizziness C0026269 Mitral valve stenosis HSDN C0020305 Fetal edema C0026697 Mucolipidoses HSDN C0018524 Hallucinate C3888102 Frontotemporal dementia with motor neuron disease MalaCards C2203646 Jaundice C0020517 Hypersensitivity HSDN C0007859 Pain neck C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0013404 Respiratory difficulty C0039239 Sinus tachycardia HSDN C0015469 Facial paralysis C0043540 Zygomatic fracture HSDN C0241210 Speaking delay C2678046 Mental retardation, x-linked, syndromic, turner type OrphaNet|HPO C0012833 Dizzy C2984330 Chagas disease pathway HSDN C0242936 Center pain C1258666 Myxoid cyst HSDN C0018991 Paralysis one side of body C0017181 Gastrointestinal hemorrhage HSDN C0151786 Weakness muscle C0597109 Nurse's role HSDN C0857305 Thrombocytopenia purpura C0000833 Abscess HSDN C0002962 Angina C0020503 Hyperparathyroidism, secondary HSDN C1962972 Proteinuria adverse event C0005974 Bone resorption HSDN C0009460 Communication impairment C3244301 Coverage level - family HSDN C1963091 Diarrhea adverse event C0018565 Acquired deformity of hand, nos HSDN C0009792 Consciousness disorder C0016735 Frontal sinusitis HSDN C3827868 Tachycardia by ecg finding C2936779 Hydroxymethylbilane synthase deficiency MalaCards C3898969 Have been vomiting C0752181 Central nervous system parasitic infections HSDN C1963281 Vomiting adverse event C0023903 Liver neoplasms HSDN C4084768 Usual severity vomiting C0037928 Spinal cord diseases HSDN C0018989 Paresis of one side of body C3809173 Epileptic encephalopathy, early infantile, 16 MalaCards|UMLS C1962956 Flatulence adverse event C0080274 Urinary retention HSDN C0015672 Decreased energy C0026640 Mouth neoplasms HSDN C4084784 Diarrhea C0020443 Hypercholesterolemia HSDN C1963281 Vomiting adverse event C0007193 Cardiomyopathy, dilated HSDN C1069915 Vertigo C2675211 Episodic ataxia, type 6 (disorder) MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0016664 Fatigue fracture HSDN C0034150 Skin purpura C0026766 Multiple organ failure HSDN C1384606 Dyspareunia C1997249 Neuralgia, pudendal MalaCards C4085548 Usual severity dizziness C0022701 Kinesthesia HSDN C1549543 Administration method - pain C0013589 Ectromelia HSDN C1557397 Adverse event associated with pain C0334533 Arteriovenous hemangioma HSDN C4084773 Bothered by weight gain C1285261 Fetal nutrition disorders HSDN C0034150 Skin purpura C0034069 Pulmonary fibrosis HSDN C0007758 Cerebellar ataxia C0042170 Uveomeningoencephalitic syndrome HSDN C0037763 Spasm C0025007 Measles HSDN C1145670 Failure respiratory C2678055 Myopathy, x-linked, with postural muscle atrophy (disorder) MalaCards|HPO C3274924 Have been coughing C0702221 Tactual discrimination HSDN C0012833 Dizzy C0004096 Asthma HSDN C0000737 Abdomen pain C0019288 Hernia, femoral HSDN C2024878 Cardiovascular surgery result: dyspnea C0034531 Experimental radiation injuries HSDN C1549543 Administration method - pain C0026636 Mouth diseases HSDN C4084725 Usual severity cough C0014461 Granuloma eosinophilic MalaCards C0019209 Large liver C0206141 Idiopathic hypereosinophilic syndrome HPO C0027066 Myoclonic jerking C1835614 Hereditary hyperexplexia MalaCards|HPO|UMLS C0427055 Face weakness C1869123 Limb-girdle muscular dystrophy type 2a MalaCards|HPO C1963281 Vomiting adverse event C0152942 Enteric tularemia nos DiseaseOntology|MalaCards C1963170 Hypothermia adverse event C0011581 Depressive disorder HSDN C4085210 Usual severity pain C0019050 Hemoglobinuria, paroxysmal HSDN C0037383 Sneeze C0035317 Retinal hemorrhage HSDN C0242936 Center pain C0008350 Cholelithiasis HSDN C0002170 Alopecia disorders C2700553 Omenn syndrome OrphaNet|HPO|MalaCards C3887873 Hearing loss C0023003 Langer-giedion syndrome MalaCards C4084768 Usual severity vomiting C0024919 Behavior, maternal HSDN C0002962 Angina C1553188 Hemolysis - observation HSDN C0030486 Extremity paralysis, lower C1134719 Invasive ductal breast carcinoma HSDN C0008031 Pain chest C0262655 Recurrent urinary tract infection HSDN C0042963 Symptoms vomiting C0026640 Mouth neoplasms HSDN C0152149 Mittelschmerz C0025345 Menstruation disturbances UMLS C0522224 Palsied C0025284 Meningeal neoplasms HSDN C2911647 Weight gain adverse event C0003838 Arterial occlusive diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027809 Neurilemmoma MalaCards C0231528 Muscle pain generalized C0473876 Cryptogenic tularaemia MalaCards C0162298 Stiffness joints C0152441 Madelung deformity MalaCards C4085661 Usual severity nausea C0007273 Carotid artery diseases HSDN C1384666 Decreased hearing C0036161 Sandhoff disease OrphaNet C1963093 Dizziness adverse event C0010674 Cystic fibrosis HSDN C2237041 Shox gene with short stature C1969056 Leopard syndrome 2 MalaCards|HPO C0010200 Cough symptom C1136033 Cutaneous mastocytosis MalaCards C0035232 Diaphragmatic paralysis C0014013 Empyema, pleural HSDN C0027796 Neuralgias C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0009421 Comatose C0026857 Musculoskeletal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0000880 Acanthamoeba keratitis HSDN C0030193 Sense of pain C1720777 Functional laterality HSDN C4049602 Hyperactivity C1863959 Hyperthyroidism, familial gestational OrphaNet|HPO|MalaCards C0019825 Voice hoarseness C1842586 Neuropathy, hereditary sensory and autonomic, type i, with cough and gastroesophageal reflux UMLS C2911647 Weight gain adverse event C0035457 Rhinitis, allergic, perennial HSDN C0700590 Diaphoresis excessive C0005859 Bloom syndrome MalaCards|HPO C4084769 Vomiting frequency C0033289 Family relationship, professional HSDN C2919142 Short stature adverse event C0001768 Agammaglobulinemia MalaCards C0018681 Headache, cephalalgia C0014077 Leukoencephalitis, acute hemorrhagic HSDN C0033790 Pseudobulbar palsy C0037773 Spastic paraplegia, hereditary HSDN C0426579 Anorexia symptom C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C0013421 Dystonia C0022758 Kap HSDN C2203646 Jaundice C0003486 Aortic aneurysm HSDN C0009763 Conjunctiva inflammation C2936917 Infantile polyarteritis MalaCards C1963252 Tremor adverse event C0919524 Atm gene HPO C4085317 Diarrhea frequency C0013289 Duodenal diseases HSDN C1384666 Decreased hearing C3550903 Cornelia de lange syndrome 5 MalaCards C0026838 Spasticity muscle C0560651 Spinal cord syndrome central HSDN C0231616 Beevor sign C0238288 Muscular dystrophy, facioscapulohumeral MalaCards|HPO C0018772 Deafness C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C4050613 Anxiety C1578691 Congenital myxedema MalaCards C0478144 Other and unspecified speech disturbances C0154725 Oth disorder nervous system UMLS C4085317 Diarrhea frequency C0027022 Myeloproliferative disease HSDN C1510417 Apraxia of gait C0007789 Cerebral palsy HSDN C1963087 Constipation adverse event C0025289 Meningitis HSDN C0344315 Mood depressed C0566602 Primary sclerosing cholangitis MalaCards|HPO C0013404 Respiratory difficulty C0862792 Stage iiia adenocarcinoma of lung UMLS C0267373 Bleeding intestine C0346072 Blue rubber bleb nevus syndrome OrphaNet|HPO|MalaCards C0009398 Color vision defects C0036341 Schizophrenia HSDN C0004134 Dyssynergia C0796123 Cataract-ataxia-deafness-retardation syndrome OrphaNet|MalaCards C0151889 Reflexes tendon increased C1865864 Amyotrophic lateral sclerosis 5 MalaCards|HPO C0037199 Sinus infection C0015773 Felty syndrome OrphaNet|MalaCards C1963087 Constipation adverse event C0037397 Behavior social HSDN C2984058 Have pain C2267227 Bulimia nervosa HSDN C0011168 Disorder deglutition C0017921 Glycogen storage disease type ii OrphaNet|MalaCards C0018784 Deafness sensorineural C0023343 Leprosy HSDN C0037763 Spasm C0392702 Abnormal involuntary movement UMLS C1963087 Constipation adverse event C0042029 Urinary tract infection HSDN C0015469 Facial paralysis C1848030 Hypotonia-cystinuria syndrome MalaCards C0018772 Deafness C2219717 Menstrual periods stopped for over 6 months HSDN C0037316 Not enough sleeping C0021125 Impulsive behavior HSDN C3898969 Have been vomiting C0022408 Arthropathy HSDN C0013456 Pain ear C0025284 Meningeal neoplasms MalaCards C0040034 Thrombocytopenia C0221021 Microangiopathic hemolytic anemia MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1299624 Postural orthostatic tachycardia syndrome HSDN C1557397 Adverse event associated with pain C0028242 Nocardia infections HSDN C1963071 Back pain adverse event C0024314 Lymphoproliferative disorders HSDN C0700078 Deep tendon reflex decrease C0270912 Charcot-marie-tooth disease, type ib HPO C0000737 Abdomen pain C0151744 Myocardial ischemia HSDN C0242936 Center pain C1176475 Ductal carcinoma HSDN C0018772 Deafness C0085136 Central nervous system neoplasms HSDN C2984057 Have nausea C1546949 Event consequence - death HSDN C0237326 Defecation pain C0018523 Hallervorden-spatz syndrome OrphaNet|MalaCards C0007398 Catatonic C0013386 Dyskinesia, drug-induced HSDN C3541349 Syncope C0013364 Dysautonomia, familial HSDN C0751837 Gait ataxic C1266180 Large cell medulloblastoma UMLS C4084897 Sleep disturbance subordinate domain C0008312 Primary biliary cirrhosis MalaCards C4085317 Diarrhea frequency C0009917 Contracture HSDN C0002170 Alopecia disorders C3810325 Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis MalaCards C0497247 Blood pressure elevation C0342739 Trimethylaminuria MalaCards|HPO C0151889 Reflexes tendon increased C0033800 Pseudoglioma MalaCards C0233794 Memory impaired C1333990 Hereditary nonpolyposis colorectal cancer MalaCards|HPO C0020673 Hypothermia (central) (local) C0028768 Obsessive-compulsive disorder HSDN C4084784 Diarrhea C0016978 Gallbladder neoplasm HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0036690 Septicemia HSDN C0032617 High urine output C0014544 Epilepsy HSDN C1279888 Proteinuria of undiagnosed cause C0019360 Herpes zoster disease HSDN C4042891 Sleep wake disorders C0026598 Movement perception HSDN C1384666 Decreased hearing C0027439 Nasopharyngeal neoplasms HSDN C0042798 Vision dim C4015388 Mccrp2 MalaCards C0026838 Spasticity muscle C3179455 Niemann-pick disease, type c1 MalaCards|HPO|UMLS C4085642 Level of joint stiffness C2748910 Rett syndrome, atypical MalaCards C0040822 D tremors C2931542 Shapiro syndrome OrphaNet|MalaCards C0018991 Paralysis one side of body C0010823 Cytomegalovirus infections HSDN C0917816 Deficiency mental C1849113 Spastic paresis, glaucoma, and mental retardation MalaCards C3665346 Loss sight C0010481 Cushing syndrome HPO C0152116 Torticollis spasmodic C3554374 Dystonia 24 MalaCards C3815497 Cough C0852007 Scleroderma and associated disorders OrphaNet C0020672 Body temperature decreased C0005591 Avian disease HSDN C0237326 Defecation pain C0220704 Shprintzen syndrome OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0853986 Lymphocytes decreased HSDN C4084775 Usual severity weight loss C0038454 Cerebrovascular accident HSDN C0019825 Voice hoarseness C1837541 Spinocerebellar ataxia 20 MalaCards C0575081 Abnormal gait C0574084 3-methylglutaconic aciduria type 3 MalaCards|HPO C0033774 Skin pruritus C2700204 Follicular variant peripheral t-cell lymphoma UMLS C0155552 Hearing loss mixed C1556061 Electric injuries HSDN C1961131 Cough adverse event C0524851 Neurodegenerative disorders HSDN C0278061 Mental status altered C1857276 Trichohepatoenteric syndrome MalaCards C4084773 Bothered by weight gain C1253937 Pericardial effusion HSDN C1963281 Vomiting adverse event C0017536 Giardiasis DiseaseOntology|HSDN C0005779 Clotting C0026205 Miosis disorder MalaCards C0242936 Center pain C0005935 Bone conduction HSDN C0013395 Indigestion C0062527 Hepatitis b vaccine HSDN C0015672 Decreased energy C0152998 Acute nonparalytic poliomyelitis, poliovirus, unspecified type DiseaseOntology|MalaCards C3829611 Nausea frequency C0038454 Cerebrovascular accident HSDN C4085641 Level of joint pain C1838280 Epiphyseal dysplasia, multiple, 1 MalaCards C0727671 Red cross toothache drops C1000483 Genus anemia HSDN C0020450 Hyperemesis gravidarum C0227791 Discharge vaginal HSDN C0018772 Deafness C1849453 Rapadilino syndrome MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1861848 Paragangliomas 4 MalaCards C0018784 Deafness sensorineural C1850510 Sialidosis, type i OrphaNet|HPO C4084724 Usual severity constipation C0014859 Esophageal neoplasms HSDN C2032395 Pelvic pain on the left C0684743 Malignant neoplasm of muscle HSDN C0018991 Paralysis one side of body C0042075 Urologic diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0023788 Whipple disease OrphaNet|MalaCards C4084724 Usual severity constipation C0020456 Hyperglycemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0031526 Philadelphia chromosome HSDN C0018991 Paralysis one side of body C0027868 Neuromuscular diseases HSDN C0349588 Stature short C3808988 Fanconi anemia, complementation group q MalaCards C2315100 Pediatric failure to thrive C1857553 Hsd11b2, arg208cys HPO C0019521 Hiccoughs C0235032 Neurotoxicity syndromes HSDN C1384666 Decreased hearing C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C0151786 Weakness muscle C0038379 Eye deviation HSDN C0033377 Caudal displacement C1855477 Dahlberg borer newcomer syndrome MalaCards C0917801 Sleep disorder insomnia C0040021 Thromboangiitis obliterans MalaCards C0233576 Mannerism C0038273 Stereotypic movement disorder UMLS C4084776 Weight loss C0002880 Autoimmune hemolytic anemia HSDN C0427202 Atony, muscular C0267171 Idiopathic gastric stasis UMLS C1962972 Proteinuria adverse event C0023223 Leg ulcer HSDN C0008031 Pain chest C0030422 Extra-adrenal paraganglioma HSDN C0700078 Deep tendon reflex decrease C4015635 Charcot-marie-tooth disease, axonal, type 2t MalaCards C4084767 Bothered by vomiting C0004623 Bacterial infections HSDN C0018772 Deafness C0039590 Testicular neoplasms HSDN C2126131 Epistaxis from the left nostril C0014591 Epistaxis UMLS C3463815 Feel fatigue C0013808 Electroconvulsive therapy HSDN C0220982 Keto acidosis C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0036572 Convulsion C0019829 Hodgkin disease HSDN C0019521 Hiccoughs C0003803 Arnold chiari malformation HSDN C4084727 Cough frequency C0018944 Hematoma HSDN C0003862 Pain joint C0032927 Precancerous conditions HSDN C0014534 Epididymitis unspecified C0004943 Behcet syndrome MalaCards C4084788 Have dizziness C0003507 Aortic valve stenosis HSDN C2024893 Cardiovascular surgery result: fatigue C0007117 Basal cell carcinoma HSDN C4084788 Have dizziness C0026848 Myopathy HSDN C0497406 Over weight C0020542 Pulmonary hypertension HSDN C0018784 Deafness sensorineural C0032453 Polychondritis, relapsing MalaCards C3714552 Strength decreased C0751038 Cockayne syndrome, type ii UMLS C0000737 Abdomen pain C0032344 Poisoning aspects HSDN C0032285 Pneum C2750068 Roifman-chitayat syndrome MalaCards C0011168 Disorder deglutition C1704981 Hyperparathyroidism-jaw tumor syndrome OrphaNet|HPO C3898969 Have been vomiting C0016751 Hereditary fructose intolerance syndrome HSDN|HPO C0020458 Hyperhydrosis C1854961 Lisker garcia ramos syndrome MalaCards C0016382 Cutaneous vascular engorgement C0334419 Pheochromocytoma, malignant MalaCards C0009763 Conjunctiva inflammation C0271865 Autoimmune hypoparathyroidism MalaCards C4085210 Usual severity pain C0043048 Experimental water deprivation HSDN C0022346 Yellow skin C0334489 Pancreatoblastoma MalaCards|UMLS C0398650 Idiopathic thrombocytopenia purpura C0041327 Tuberculosis, pulmonary HSDN C4084773 Bothered by weight gain C0036118 Salmonella infections, animal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030286 Pancreatic diseases HSDN C0011991 Loose stools C0023434 Chronic lymphocytic leukemia HSDN C0349588 Stature short C0022716 Menkes kinky hair syndrome MalaCards|HPO C2029884 Hearing loss by exam C1762616 Meningioma, benign, no icd-o subtype HSDN C0018777 Deafness, conductive C0008928 Cleidocranial dysplasia HSDN C0008031 Pain chest C2609414 Acute kidney injury HSDN C4085211 Pain distress question C3809899 Episodic pain syndrome, familial, 3 MalaCards C1963249 Tinnitus adverse event C0007222 Cardiovascular diseases HSDN C4085548 Usual severity dizziness C0051981 Anti-leprosy vaccine HSDN C0035455 Rhinitis C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C2203646 Jaundice C0162871 Aortic aneurysm, abdominal HSDN C0033774 Skin pruritus C0263662 Disseminated eosinophilic collagen disease HSDN C0011991 Loose stools C0027658 Neoplasms, germ cell and embryonal HSDN C0036572 Convulsion C1859133 Rhizomelic chondrodysplasia punctata, type 1 HPO|UMLS C3163620 Hypotension adverse event C1335686 Neuroendocrine neoplasm of rectum MalaCards C0018681 Headache, cephalalgia C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0027868 Neuromuscular diseases HSDN C4084774 Have weight loss C0006818 Campylobacter infection HSDN C0033774 Skin pruritus C3273126 Extrahepatic bile duct adenocarcinoma, biliary type UMLS C0039070 Collapse fleeting C0007020 Carbon monoxide poisoning HSDN C0018681 Headache, cephalalgia C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1549543 Administration method - pain C0007124 Noninfiltrating intraductal carcinoma HSDN C1963184 Nystagmus adverse event C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0460137 Push down or depress C0085547 Phenylketonuria, maternal MalaCards|HPO C3274924 Have been coughing C0036690 Septicemia HSDN C4085211 Pain distress question C0020877 Ileitis HSDN C0018772 Deafness C0039538 Teratoma HSDN C0039070 Collapse fleeting C1546533 Specimen source codes - abscess HSDN C0028738 Nystagmus C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0600260 Lung diseases, obstructive HSDN C0022346 Yellow skin C0020502 Hyperparathyroidism HSDN C0005745 Blepharoptosis C0796279 Carnevale syndrome MalaCards|HPO C4085210 Usual severity pain C0035369 Retroviridae infections HSDN C2984057 Have nausea C0036690 Septicemia HSDN C0027796 Neuralgias C0997768 Glaucoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0080178 Spina bifida HSDN C0233514 Behavior abnormal C4024961 Metachromatic leukodystrophy variant MalaCards C0004134 Dyssynergia C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO|UMLS C0039070 Collapse fleeting C0035309 Retinal diseases HSDN C0085642 Asphyxia reticularis C0002992 Angiomatosis HSDN C0028738 Nystagmus C1857743 Leber congenital amaurosis 12 (disorder) MalaCards|HPO C1557397 Adverse event associated with pain C0391889 Bony union HSDN C0151889 Reflexes tendon increased C0154682 Lateral sclerosis MalaCards C0035232 Diaphragmatic paralysis C0027651 Tumor HSDN C3887873 Hearing loss C0016788 Fucosidase deficiency disease MalaCards C1963091 Diarrhea adverse event C0011881 Diabetic nephropathy HSDN C2984058 Have pain C0014394 Enuresis HSDN C2911645 Weight loss adverse event C0009375 Colonic neoplasms HSDN C0019079 Bloody sputum C0836924 Thrombocytosis HSDN C0043068 Friderichsen-waterhouse syndrome C0037997 Splenic diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0022578 Keratoconus HSDN C0002962 Angina C0032587 Polyradiculoneuropathy HSDN C0575081 Abnormal gait C2931821 Nakamura osame syndrome OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0017638 Glioma HSDN C1527344 Dysphonia C0001883 Airway obstruction HSDN C0424755 Fever symptoms C0020097 Htlv-i infections HSDN C3539022 Pelvic pain decreasing in severity C0041582 Ulcer HSDN C3829611 Nausea frequency C1837218 Cleft palate, isolated HSDN C0010520 Skin cyanosis C0268194 Phosphoenolpyruvate carboxykinase deficiency UMLS C0003079 Pupillary inequality C0038218 Status asthmaticus HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0917875 Esophageal diverticulosis HSDN C0013404 Respiratory difficulty C0014547 Epilepsies, partial HSDN C0000737 Abdomen pain C1335113 Opisthorchis viverrini-related cholangiocarcinoma UMLS C4042891 Sleep wake disorders C0040136 Thyroid neoplasm HSDN C0015970 Fever unknown origin C0796561 Melanoma vaccines HSDN C0042964 Anticipatory vomiting C0853697 Neutrophil count decreased HSDN C4085211 Pain distress question C0037928 Spinal cord diseases HSDN C0557874 Global developmental delay C4014479 Culler-jones syndrome MalaCards C1557397 Adverse event associated with pain C0042850 Vitamin b deficiency HSDN C0011991 Loose stools C1254288 Anthrax HSDN C0518090 Frequency of pain question C0001427 Adenoiditis, nos MalaCards C1963180 Neck pain adverse event C1556682 Adverse event associated with infection HSDN C0151786 Weakness muscle C4048184 Trochlear nerve diseases HSDN C1557397 Adverse event associated with pain C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C0000737 Abdomen pain C0024809 Marijuana abuse HSDN C1145670 Failure respiratory C2931347 Cardiac form of generalized glycogenosis MalaCards|HPO C1963071 Back pain adverse event C0272129 Donath-landsteiner hemolytic anemia OrphaNet|MalaCards C0018772 Deafness C0006840 Candidiasis HSDN C1963137 Hydrocephalus adverse event C1857351 Dandy walker malformation postaxial polydactyly MalaCards C4085661 Usual severity nausea C1962958 Hematoma adverse event HSDN C2911645 Weight loss adverse event C1527429 Increased blood npn HSDN C0233794 Memory impaired C0025286 Meningioma MalaCards C0011991 Loose stools C0017574 Gingivitis HSDN C0030193 Sense of pain C4060542 Impaired mood regulation UMLS C0013528 Echo speech C0001889 Akinetic mutism HSDN C0030193 Sense of pain C0018946 Hematoma, subdural HSDN C0242936 Center pain C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0035455 Rhinitis C3809548 Ciliary dyskinesia, primary, 23 MalaCards C2911645 Weight loss adverse event C0036690 Septicemia HSDN C0426579 Anorexia symptom C0334463 Malignant fibrous histiocytoma MalaCards C0917816 Deficiency mental C1970203 Polyhydramnios, megalencephaly, and symptomatic epilepsy MalaCards C0018991 Paralysis one side of body C0151699 Intracranial hemorrhages HSDN|UMLS C0007758 Cerebellar ataxia C0268242 Niemann-pick disease, type a MalaCards C2984058 Have pain C1555865 Forensic psychiatry HSDN C0018784 Deafness sensorineural C0349499 Fetal cytomegalovirus syndrome OrphaNet|MalaCards C2984057 Have nausea C0242658 Homosexuality male HSDN C4084724 Usual severity constipation C0314657 Genetic predisposition HSDN C4085641 Level of joint pain C0494043 Streptobacillosis MalaCards C0003079 Pupillary inequality C0162671 Melas syndrome HSDN C0011991 Loose stools C0006736 Body stone HSDN C0085593 Chill C1336476 Stage i mesothelioma of pleura UMLS C0036572 Convulsion C0005944 Metabolic bone disorder HSDN C0234357 Adiadokokinesis C0013384 Dyskinetic syndrome UMLS C0917816 Deficiency mental C2673873 Bardet-biedl syndrome 13 MalaCards|HPO C4084769 Vomiting frequency C0456892 Csf low pressure HSDN C3641756 Have diarrhea C0001618 Tumors of adrenal cortex HSDN C4084724 Usual severity constipation C0237873 Physiological sexual disorders HSDN C0022346 Yellow skin C0008325 Cholecystitis HPO C3539023 Pelvic pain increasing in frequency C0005940 Bone diseases HSDN C0008031 Pain chest C1334969 Nodular lymphoid hyperplasia of lung UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0001075 Achlorhydria HSDN C3463815 Feel fatigue C0013504 Echinococcosis, hepatic HSDN C0018784 Deafness sensorineural C1963274 Vasculitis adverse event HSDN C1963087 Constipation adverse event C0006840 Candidiasis HSDN C0013404 Respiratory difficulty C0007222 Cardiovascular diseases HSDN C0020615 Hypoglycemia nos C0206624 Hepatoblastoma MalaCards C4084766 Vomiting C4012395 Congenital disorder of glycosylation, type iy MalaCards C4084723 Constipation C0014858 Esophageal motility disorders HSDN C1557397 Adverse event associated with pain C0039980 Chest injury HSDN C0235031 Neurological complaint C0233796 Amnesia temporary UMLS C1963091 Diarrhea adverse event C0038012 Spondylitis HSDN C0242936 Center pain C0030354 Papilloma HSDN C2024878 Cardiovascular surgery result: dyspnea C0024118 Lung disease, parasitic HSDN C4084766 Vomiting C0010074 Coronary vessel anomalies HSDN C0032617 High urine output C0006110 Brain death HSDN C0848203 Male pelvic pain C0023895 Liver diseases HSDN C0037316 Not enough sleeping C0001723 Affective disorders, psychotic HSDN C3898969 Have been vomiting C0268543 Hyperammonemia, type iii MalaCards|HPO C0751837 Gait ataxic C0154778 Myopia, degenerative HSDN C1384666 Decreased hearing C2930927 Kallmann syndrome, type 3, recessive MalaCards C4084727 Cough frequency C0051981 Anti-leprosy vaccine HSDN C0917816 Deficiency mental C2676788 Joubert syndrome 9 (disorder) MalaCards|HPO C0857305 Thrombocytopenia purpura C2984299 Asthma pathway HSDN C0404484 Chronic female pelvic pain C0457568 Disorder of female pelvic region and peritoneum UMLS C1384666 Decreased hearing C0038013 Ankylosing spondylitis HSDN C1962972 Proteinuria adverse event C3496337 Idiopathic nephrotic syndrome MalaCards C0018784 Deafness sensorineural C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome MalaCards|HPO C0015672 Decreased energy C0022408 Arthropathy HSDN C0009792 Consciousness disorder C1412084 Abcd1 gene HSDN C2203646 Jaundice C2827407 Infectious otitis media HSDN C0019521 Hiccoughs C3489393 Hiatal hernia HSDN C2984057 Have nausea C3813607 Infantile gastroesophageal reflux HSDN C0557874 Global developmental delay C1833691 Otofaciocervical syndrome OrphaNet|HPO C0018681 Headache, cephalalgia C1333073 Clivus meningioma UMLS C1279888 Proteinuria of undiagnosed cause C0006264 Bronchial neoplasms HSDN C3665386 Abnormal vision C0751783 Lafora disease HPO C4084776 Weight loss C0344434 Atrial fibrillation ecg HSDN C0426579 Anorexia symptom C0035435 Rheumatism HSDN C0349588 Stature short C0391826 Lhermitte-duclos disease MalaCards C0454644 Delayed language development C0265210 Weaver syndrome MalaCards|HPO C1963063 Anorexia adverse event C2937358 Cerebral hemorrhage HSDN C1962972 Proteinuria adverse event C0040809 Patient refusal of treatment HSDN C1279888 Proteinuria of undiagnosed cause C0270611 Brain damage HSDN C4085211 Pain distress question C1963139 Hypopigmentation adverse event HSDN C0018681 Headache, cephalalgia C4086153 Childhood atypical choroid plexus papilloma UMLS C3665347 Vision impaired C0003076 Aniridia OrphaNet|HPO|MalaCards C0015672 Decreased energy C0023487 Acute promyelocytic leukemia HSDN C4085549 Dizziness C0752143 Intracranial thrombosis HSDN C0018784 Deafness sensorineural C0034960 Refsum disease OrphaNet|HSDN|HPO C0008033 Pain pleural C1275126 Tnf receptor-associated periodic fever syndrome (traps) UMLS C0013404 Respiratory difficulty C0036690 Septicemia HSDN C4084723 Constipation C1457883 Aggressive reaction HSDN C0036572 Convulsion C0019114 Hemosiderosis HSDN C0033377 Caudal displacement C0796012 Krause-kivlin syndrome HPO C0221263 Cafe au lait spot C0175693 Russell-silver syndrome MalaCards|HPO C0030193 Sense of pain C0085084 Motor neuron disease HSDN C4084802 Usual severity diarrhea C0009404 Colorectal neoplasms HSDN C1963086 Confusion adverse event C0009324 Ulcerative colitis HSDN C0036659 Sensation disorder C2937358 Cerebral hemorrhage HSDN C0036572 Convulsion C0020295 Hydronephrosis HSDN C0020672 Body temperature decreased C0042216 Poxvirus officinalis HSDN C4085317 Diarrhea frequency C0018923 Hemangiosarcoma HSDN C1963964 Periungual erythema C0041834 Erythema UMLS C0037199 Sinus infection C2347126 Microscopic polyarteritis MalaCards C0028738 Nystagmus C0268494 Oculocutaneous albinism type 1 MalaCards|HPO C1963170 Hypothermia adverse event C0024141 Lupus erythematosus, systemic HSDN C0036572 Convulsion C0751778 Myoclonic epilepsies, progressive HSDN|UMLS C0002962 Angina C0001144 Acne vulgaris HSDN C3539020 Pelvic pain decreasing in frequency C0243001 Abdominal abscess HSDN C0011570 Monopolar depression C0342859 Harderoporphyria HPO C1963086 Confusion adverse event C0036992 Short bowel syndrome HSDN C1971624 Appetite absent C1112486 Aggressive systemic mastocytosis MalaCards C0700078 Deep tendon reflex decrease C1854058 Spinal muscular atrophy, late-onset, finkel type MalaCards|HPO C0009806 Constipate C0039128 Syphilis HSDN C3829611 Nausea frequency C0031039 Effusion pericardial HSDN C0018681 Headache, cephalalgia C1334829 Multiple skull base meningiomas UMLS C0497406 Over weight C0001430 Adenoma HSDN C0004604 Pain back C0022660 Kidney failure, acute HSDN C1963093 Dizziness adverse event C0039231 Tachycardia HSDN C4084766 Vomiting C0037928 Spinal cord diseases HSDN C0033377 Caudal displacement C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C3641756 Have diarrhea C4084971 Trachoma HSDN C4084766 Vomiting C2945767 Childhood liver cancer MalaCards C0036396 Sciatica C0152025 Polyneuropathy HSDN C0086437 Joint hypermobility C2700425 Ehlers-danlos syndrome, dermatosparaxis type HPO C0015300 Ocular proptosis C1851719 Beckwith-wiedemann syndrome chromosome region HPO C2984058 Have pain C0556482 Protection sex HSDN C4084723 Constipation C0042251 Vaginal diseases HSDN C0042510 Fibrillation paroxysmal vent C1142166 Brugada syndrome (disorder) HPO C0009806 Constipate C0033822 Pseudomyxoma peritonei MalaCards C0015672 Decreased energy C2752015 Glycogen storage disease xiv MalaCards|UMLS C0151786 Weakness muscle C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards C1549543 Administration method - pain C0023364 Leptospirosis HSDN C4084723 Constipation C1859049 Cchs with hirschsprung disease MalaCards|HPO C4084723 Constipation C0520946 Emotional hypersensitivity HSDN C4084767 Bothered by vomiting C0022658 Kidney diseases HSDN C1557397 Adverse event associated with pain C0013117 Dreaming HSDN C4085317 Diarrhea frequency C0262584 Carcinoma, small cell HSDN C1971624 Appetite absent C2239176 Liver carcinoma MalaCards C1963184 Nystagmus adverse event C3810363 Bosch-boonstra-schaaf optic atrophy syndrome MalaCards C2315100 Pediatric failure to thrive C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C1000483 Genus anemia C0334123 Histiocytosis, lipoid MalaCards C0018681 Headache, cephalalgia C0027338 Biting nail HSDN C0011991 Loose stools C0007095 Carcinoid tumor HSDN C0038002 Spleen enlargement C0012236 Digeorge syndrome MalaCards|HPO C0413252 Hypothermia due to exposure C0017612 Glaucoma, open-angle HSDN C4085210 Usual severity pain C0042900 Vitiligo HSDN C0233993 Sexuality related problems C0234022 Anorgasmia UMLS C0024031 Back pain lower back C1881674 Medical device emits smoke HSDN C4084727 Cough frequency C0019372 Herpesviridae infections HSDN C0917816 Deficiency mental C3280284 Mental retardation, autosomal dominant 10 MalaCards C4085317 Diarrhea frequency C0011848 Diabetes insipidus HSDN C1069915 Vertigo C1706377 Memory device component HSDN C0242936 Center pain C0085632 Apathy HSDN C1384666 Decreased hearing C0037928 Spinal cord diseases HSDN C0027497 Queasy C0006264 Bronchial neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016483 Food preferences HSDN C0518090 Frequency of pain question C1963139 Hypopigmentation adverse event HSDN C0013404 Respiratory difficulty C0080179 Vertebra fracture HSDN C0206146 Myocardial stunning C2004491 Cicatrix HSDN C0015468 Face pain C3810814 Myocardial infarction ecg assessment HSDN C3163620 Hypotension adverse event C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C3641756 Have diarrhea C0039614 Tetanus HSDN C0013604 Edematous C0038358 Gastric ulcer HSDN C3829611 Nausea frequency C0039730 Thalassemia HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0009241 Cognition disorders HSDN C0008031 Pain chest C0015695 Fatty liver HSDN C0042963 Symptoms vomiting C1705714 Lats1 wt allele HSDN C2024878 Cardiovascular surgery result: dyspnea C0006287 Bronchopulmonary dysplasia MalaCards C0015230 Exanthem C0033847 Pseudoxanthoma elasticum OrphaNet|HPO|MalaCards C3887873 Hearing loss C0017636 Glioblastoma HSDN C0242936 Center pain C1963059 Adrenal insufficiency adverse event HSDN C0587050 Lower extremity mass C1290133 Melanocytic naevus of lower limb UMLS C0002962 Angina C0013370 Amebic colitis HSDN C0018775 Hearing loss bilateral C0011989 Camurati-engelmann syndrome HSDN C0018989 Paresis of one side of body C1846388 Cortical dysplasia of taylor, dysplasia only HPO C4084784 Diarrhea C0151467 Addisonian crisis OrphaNet|MalaCards C0040264 Ear ringing sound C0814263 Meditation therapy HSDN C0239574 Fever low grade C0008677 Bronchitis, chronic DiseaseOntology|MalaCards C3463815 Feel fatigue C0018801 Heart failure HSDN C0004134 Dyssynergia C0206727 Nerve sheath tumors HSDN C0152165 Vomiting persistent C1857855 Spastic paraplegia 29, autosomal dominant MalaCards|UMLS C2242996 Tingling C1384672 Hpt gene HSDN C0030486 Extremity paralysis, lower C1090821 Sepsis (invertebrate) HSDN C0042571 Vertigo subjective C0012691 Dislocations HSDN C0151786 Weakness muscle C4015624 Myopathy, vacuolar, with casq1 aggregates MalaCards C0009421 Comatose C0009492 Compartment syndromes HSDN C0085636 Light sensitivity C0042376 Vascular headaches HSDN C2880347 Corneal deposits in metabolic disorders, unspecified eye C0015397 Disorder of eye UMLS C4085549 Dizziness C0039538 Teratoma HSDN C2237041 Shox gene with short stature C3151218 Osteogenesis imperfecta, type xi MalaCards|HPO C0848203 Male pelvic pain C0011854 Diabetes mellitus, insulin-dependent HSDN C4085211 Pain distress question C0032533 Polymyalgia rheumatica HSDN C0018777 Deafness, conductive C0016508 Congenital foot deformity HSDN C2911645 Weight loss adverse event C0559260 Congenital scoliosis HSDN C0497247 Blood pressure elevation C0001231 Acth syndrome, ectopic MalaCards C4084774 Have weight loss C0271737 Addison's disease due to autoimmunity OrphaNet C0009421 Comatose C1621920 Intermediate maple syrup urine disease HPO C1557397 Adverse event associated with pain C1532560 Plasmacytoma - category HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0037354 Smallpox HSDN C0000737 Abdomen pain C0002871 Anemia UMLS C4084787 Have difficulty swallowing C0396023 Chronic adenoiditis DiseaseOntology|MalaCards C0027497 Queasy C0023220 Leg injury HSDN C0018681 Headache, cephalalgia C0020502 Hyperparathyroidism HSDN C4049644 Depression C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C2237041 Shox gene with short stature C1854663 Chudley rozdilsky syndrome OrphaNet|MalaCards C0003862 Pain joint C0001349 Acute-phase reaction HSDN C0030193 Sense of pain C0280396 Laryngeal verrucous carcinoma, stage ii UMLS C0011570 Monopolar depression C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C3815497 Cough C0037361 Olfactory sense HSDN C0030794 Pelvis pain C0009324 Ulcerative colitis HSDN C2936821 Spinal cerebrospinal fluid leak C0020225 Hydranencephaly HSDN C4084802 Usual severity diarrhea C0025309 Meningoencephalitis HSDN C0020450 Hyperemesis gravidarum C0438692 Vaginal discharge symptom HSDN C0004134 Dyssynergia C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0233565 Bradykinesia C3550973 Neurodegeneration with brain iron accumulation 5 UMLS C4084769 Vomiting frequency C0007787 Transient ischemic attack HSDN C0521591 Mouth paresthesia C0030554 Paresthesia UMLS C4085210 Usual severity pain C0852795 Increased insulin level HSDN C0241137 Skin pallor C0002886 Anemia, macrocytic HSDN C0460137 Push down or depress C1862939 Amyotrophic lateral sclerosis 1 MalaCards C0033774 Skin pruritus C0010709 Cyst HSDN C0235153 Sensory hallucination C2675891 Chromosome 1q21.1 duplication syndrome MalaCards C0036572 Convulsion C3714514 Infection HSDN C4084802 Usual severity diarrhea C0027868 Neuromuscular diseases HSDN C0851578 Disorder sleep C0037650 Somatoform disorder HSDN C0018772 Deafness C2931280 Congenital alopecia, psychomotor retardation, convulsions OrphaNet|HPO|MalaCards C0020672 Body temperature decreased C0015802 Femur fracture HSDN C3539893 Pelvic pain occurs with intercourse C0042029 Urinary tract infection HSDN C0036572 Convulsion C1332906 Cerebral glioblastoma UMLS C2984058 Have pain C0016171 Fistula of intestine, excluding rectum and anus HSDN C0518090 Frequency of pain question C0037019 Shy-drager syndrome HSDN C4085211 Pain distress question C0032302 Mycoplasma pneumonia HSDN C1069915 Vertigo C0032343 Poisoning HSDN C1579931 Depressed - symptom C0002986 Fabry disease MalaCards|HPO C1961131 Cough adverse event C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN C1260880 Nasal drip C0280387 Lymphoepithelioma of the nasopharynx, recurrent UMLS C0242936 Center pain C0037052 Sick sinus syndrome HSDN C0344435 Ventricular fibrillation by ecg finding C3697638 Familial short qt syndrome MalaCards C0035229 Respiratory function impaired C3714644 Thymus neoplasms MalaCards C0398650 Idiopathic thrombocytopenia purpura C0038356 Stomach neoplasms HSDN C0018989 Paresis of one side of body C0035439 Rheumatic heart disease UMLS C3539896 Pelvic pain occurs with urination C0016542 Foreign body HSDN C0018989 Paresis of one side of body C0162671 Melas syndrome MalaCards|HPO|UMLS C0237326 Defecation pain C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0011991 Loose stools C0031345 Pharyngeal diseases HSDN C0424755 Fever symptoms C0041955 Ureteral neoplasms HSDN C0151786 Weakness muscle C0038356 Stomach neoplasms HSDN C4084784 Diarrhea C1299262 Sarcoma - category (morphologic abnormality) HSDN C4084723 Constipation C0334299 Carcinoid tumor no icd-o subtype HSDN C4084773 Bothered by weight gain C0012979 Canine disease HSDN C3541349 Syncope C0020443 Hypercholesterolemia HSDN C2029884 Hearing loss by exam C0003962 Ascites HSDN C0271215 Blindness legal C1864987 Migraine, familial hemiplegic, 3 MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037286 Skin neoplasms HSDN C0004604 Pain back C0007781 Intracranial embolism and thrombosis HSDN C0151740 Intracranial hypertension C2675746 Craniodiaphyseal dysplasia, autosomal dominant (disorder) HPO C1963091 Diarrhea adverse event C0031873 Pica disease HSDN C0008031 Pain chest C0010709 Cyst HSDN C2029884 Hearing loss by exam C0020433 Hyperbilirubinemia HSDN C2029884 Hearing loss by exam C0079744 Diffuse large b-cell lymphoma HSDN C0162298 Stiffness joints C0043119 Werner syndrome MalaCards|HPO C4085211 Pain distress question C0282550 Persian gulf syndrome HSDN C0003811 Cardiac rhythm disturbance C0041409 Turner syndrome, male MalaCards C4084784 Diarrhea C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0033790 Pseudobulbar palsy C0011633 Dermatomyositis HSDN C3829611 Nausea frequency C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C1557397 Adverse event associated with pain C0021833 Intestinal fistula HSDN C1527344 Dysphonia C0027651 Tumor HSDN C4084784 Diarrhea C0085178 Needle stick injury HSDN C0234132 Pyramidal sign C3806634 Deafness, dystonia, and cerebral hypomyelination MalaCards|UMLS C4084723 Constipation C0393571 Multiple system atrophy HSDN C0018681 Headache, cephalalgia C0795953 Masa syndrome (disorder) MalaCards C0042963 Symptoms vomiting C0302148 Blood clot HSDN C0242936 Center pain C0752347 Lewy body disease HSDN C0522224 Palsied C0003708 Arachnitis HSDN C2203646 Jaundice C1527429 Increased blood npn HSDN C3815497 Cough C0035435 Rheumatism HSDN C0018784 Deafness sensorineural C3808964 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0860603 Anxiety symptoms HSDN C4042891 Sleep wake disorders C0030922 Peptic ulcer hemorrhage HSDN C3641756 Have diarrhea C0042063 Urogenital abnormalities HSDN C0022107 Fussiness C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0018932 Bright red rectal bleeding C1411077 Ragpicker's disease MalaCards C0009792 Consciousness disorder C0033941 Psychoses, substance-induced HSDN C0917816 Deficiency mental C4014414 Mental retardation, autosomal dominant 24 MalaCards C4084784 Diarrhea C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4084766 Vomiting C3888018 Congenital hyperinsulinism MalaCards C1963252 Tremor adverse event C1290398 Cerebral arterial aneurysm HSDN C4084768 Usual severity vomiting C0524812 Intracranial hypotension HSDN C0030552 Paralysis partial C1510415 Osteosclerotic myeloma MalaCards C0030552 Paralysis partial C1412084 Abcd1 gene HSDN C4085548 Usual severity dizziness C0031212 Personality disorders HSDN C0036572 Convulsion C0024141 Lupus erythematosus, systemic MalaCards|UMLS C1963091 Diarrhea adverse event C0085605 Liver failure HSDN C1527344 Dysphonia C0268242 Niemann-pick disease, type a MalaCards C4085862 Bothered by nausea C0017658 Glomerulonephritis HSDN C0036572 Convulsion C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards|UMLS C4084775 Usual severity weight loss C0853697 Neutrophil count decreased HSDN C0004604 Pain back C0003486 Aortic aneurysm HSDN C0042571 Vertigo subjective C0015467 Neuralgia facial HSDN C4084726 Distress cough C1299919 Enteric coccidiosis HSDN C0234146 Absent reflex C1839566 Charcot-marie-tooth disease, x-linked recessive, 5 OrphaNet|HPO|MalaCards C0473137 Congenital faecal incontinence C0015732 Fecal incontinence UMLS C1963252 Tremor adverse event C2931125 Feigenbaum bergeron richardson syndrome OrphaNet|MalaCards C0018991 Paralysis one side of body C1860403 Congenital bilateral recurrent nerve paralysis and ptosis MalaCards C0013362 Dysarthrias C0376527 Neoplasm, skull base HSDN C1963281 Vomiting adverse event C0162576 Anisakiasis HSDN C0030554 Abnormal sensation C0043251 Wounds and injuries HSDN C4084769 Vomiting frequency C0015814 Femur head necrosis HSDN C0036572 Convulsion C0013370 Amebic colitis HSDN C2984058 Have pain C0030569 Secondary parkinson disease HSDN C0018681 Headache, cephalalgia C0039730 Thalassemia HSDN C0034933 Abnormal reflexes C0003466 Anus, imperforate HSDN C2984058 Have pain C0022078 Iris diseases HSDN C0080233 Dental loss C0029294 Orofaciodigital syndromes MalaCards C0149793 Transient monocular blindness C0032461 Polycythemia HSDN C4085661 Usual severity nausea C0020875 Ileal diseases HSDN C0030193 Sense of pain C0018924 Hemarthrosis HSDN C4084768 Usual severity vomiting C0152942 Enteric tularemia nos DiseaseOntology|MalaCards C0035078 Failure kidney C0036472 Scrub typhus MalaCards C4085317 Diarrhea frequency C0030636 Pasteurella infection HSDN C3829611 Nausea frequency C0266836 Infantile colic HSDN C4084766 Vomiting C0238154 Epidural hematoma HSDN C1963184 Nystagmus adverse event C1848519 Waardenburg syndrome, type 4a MalaCards|HPO C0349588 Stature short C0431406 Asymmetric crying face association OrphaNet|HPO|MalaCards C1963137 Hydrocephalus adverse event C2985524 Rhabdoid tumor predisposition syndrome MalaCards C4085661 Usual severity nausea C0026857 Musculoskeletal diseases HSDN C4085211 Pain distress question C0032066 Plague vaccines HSDN C0030193 Sense of pain C0027583 Nematode infections HSDN C0013404 Respiratory difficulty C1336173 Stage iia squamous cell carcinoma of lung UMLS C1963091 Diarrhea adverse event C0022548 Keloid HSDN C0007758 Cerebellar ataxia C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0234146 Absent reflex C1861669 Charcot-marie-tooth disease and deafness HPO C0009676 Confusion state C0086032 Chromatic vision HSDN C1549543 Administration method - pain C0282488 Interstitial cystitis OrphaNet|MalaCards C0575081 Abnormal gait C0027859 Acoustic neuroma HPO C3539891 Pelvic pain to the rear C2936403 46, xx disorders of sex development HSDN C0011991 Loose stools C0267663 Congenital secretory diarrhea, sodium type (disorder) UMLS C2984057 Have nausea C0021359 Infertility HSDN C0010520 Skin cyanosis C0003492 Aortic coarctation HSDN C4084776 Weight loss C0001624 Adrenal gland neoplasms HSDN C3829611 Nausea frequency C0019080 Hemorrhage HSDN C0233514 Behavior abnormal C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C0010200 Cough symptom C0220981 Metabolic acidosis HSDN C1557397 Adverse event associated with pain C0001422 Adenofibroma HSDN C4085862 Bothered by nausea C1260386 Glucocorticoid-remediable aldosteronism HPO C0518090 Frequency of pain question C0030767 Grouping peer HSDN C0019209 Large liver C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C4085211 Pain distress question C1509147 Histiocytoma HSDN C0011168 Disorder deglutition C0024408 Machado-joseph disease MalaCards|HPO C0151908 Dry skin C3279807 Ced3 MalaCards|UMLS C4084769 Vomiting frequency C0017155 Gastritis, hypertrophic HSDN C0022346 Yellow skin C1333067 Clear cell carcinoma of liver cells UMLS C0003467 Angst C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C1971624 Appetite absent C0740277 Bile duct carcinoma HPO C4025811 Anemic pallor C3468041 Fanconi anemia, complementation group c MalaCards C0042798 Vision dim C2931404 Albright's hereditary osteodystrophy MalaCards C0027497 Queasy C0032326 Pneumothorax HSDN C0270948 Neurogenic muscular atrophy C2931376 Hapnes boman skeie syndrome MalaCards C2029884 Hearing loss by exam C0012979 Canine disease HSDN C1384666 Decreased hearing C1868570 Char syndrome MalaCards|HPO C0085649 Edema extremities C0026691 Mucocutaneous lymph node syndrome DiseaseOntology|MalaCards C0026826 High muscle tone C0266470 Cerebellar hypoplasia OrphaNet C0268988 Itch penis C1290866 Disease of pelvis UMLS C0036572 Convulsion C0040034 Thrombocytopenia HSDN|UMLS C3539889 Pelvic pain increasing in severity C0020550 Hyperthyroidism HSDN C1963091 Diarrhea adverse event C0029400 Osteitis HSDN C0007815 Cerebrospinal fluid rhinorrhoea C1090821 Sepsis (invertebrate) HSDN C1963184 Nystagmus adverse event C1852759 Papillorenal syndrome MalaCards|HPO C4084774 Have weight loss C1253943 Fluid in the chest HSDN C0242936 Center pain C0149678 Epstein-barr virus infections HSDN C4084767 Bothered by vomiting C0039980 Chest injury HSDN C0518090 Frequency of pain question C0036239 Satiety HSDN C0013132 Drooling C1856113 Mowat-wilson syndrome MalaCards|HPO C0004604 Pain back C0008066 Child behavior disorders HSDN C0013604 Edematous C0009395 Color perception HSDN C1962972 Proteinuria adverse event C0022865 Obstetric labor complications HSDN C4084775 Usual severity weight loss C0010692 Cystitis HSDN C1963274 Vasculitis adverse event C0221056 Adult type dermatomyositis MalaCards C0018772 Deafness C0717360 Disease lyme vaccine HSDN C0018524 Hallucinate C0051981 Anti-leprosy vaccine HSDN C2315100 Pediatric failure to thrive C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C0015402 Hemorrhage eye C0035335 Retinoblastoma HSDN C1549543 Administration method - pain C0751878 Vasculitis, central nervous system HSDN C0237326 Defecation pain C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0020458 Hyperhydrosis C1275808 Congenital central hypoventilation MalaCards|HPO C0018772 Deafness C1548777 Specimen reject reason - hemolysis HSDN C1963091 Diarrhea adverse event C0039240 Supraventricular tachycardia HSDN C0036659 Sensation disorder C0271375 Cranial nerve palsy iv trochlear HSDN C0269671 Gestational edema without mention of hypertension C0341960 Edema pregnancy UMLS C0151786 Weakness muscle C1000483 Genus anemia HSDN C1535893 Orthostatic intolerance C0039231 Tachycardia HSDN C0013404 Respiratory difficulty C2984289 Melanoma pathway HSDN C2167935 Pain in left wrist C0810350 Non-traumatic joint disorders UMLS C0406406 Persisting cholinergic urticaria C0152230 Cholinergic urticaria UMLS C0030193 Sense of pain C0008533 Hemophilia b HSDN C0036396 Sciatica C0036677 Sensory threshold HSDN C0011991 Loose stools C0242658 Homosexuality male HSDN C2037135 Sudden loss of vision in temporal half of visual field C2037137 Sudden loss left vision left UMLS C4085549 Dizziness C0242287 Isaacs syndrome HSDN C0022346 Yellow skin C0023869 Lithiasis HSDN C1962972 Proteinuria adverse event C0342623 Senile systemic amyloidosis MalaCards C0019079 Bloody sputum C0684249 Carcinoma of lung DiseaseOntology|UMLS C0018784 Deafness sensorineural C2675730 Deafness, congenital, and onychodystrophy, autosomal dominant HPO C2919142 Short stature adverse event C1844887 Catel manzke syndrome OrphaNet|HPO|MalaCards C0150055 Pain chronic C0018802 Congestive heart failure HSDN C0241165 Skin thickening C0917715 Hajdu-cheney syndrome HPO C0013404 Respiratory difficulty C1333420 Epithelial predominant pulmonary blastoma UMLS C0043094 Weight gain C0001249 Actinobacillus infections HSDN C1549543 Administration method - pain C0015458 Facial hemiatrophy HSDN C0557874 Global developmental delay C3281191 Epileptic encephalopathy, early infantile, 13 MalaCards C0518090 Frequency of pain question C0015556 Fallopian tube diseases HSDN C1963071 Back pain adverse event C0020615 Hypoglycemia HSDN C4084788 Have dizziness C1306759 Eosinophilic disorder HSDN C0023015 Language handicap C0525045 Mood disorders HSDN C0034151 Hyperglobulinemic purpura C0037274 Dermatologic disorders HSDN C0030794 Pelvis pain C1394494 Cystocele, unspecified HSDN C0018681 Headache, cephalalgia C0031351 Pharyngoconjunctival fever DiseaseOntology|MalaCards C0034150 Skin purpura C0002992 Angiomatosis HSDN C0518090 Frequency of pain question C0041326 Pleural tuberculosis HSDN C4085317 Diarrhea frequency C1546949 Event consequence - death HSDN C0036572 Convulsion C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|UMLS|HPO|MalaCards C3274924 Have been coughing C0153415 Malignant neoplasm of lower third of esophagus MalaCards C2984057 Have nausea C0428977 Bradycardia HSDN C0004134 Dyssynergia C0034065 Pulmonary embolism HSDN C0521532 Diaphragmatic weakness C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C0018524 Hallucinate C1854182 Parkinson disease 4, autosomal dominant lewy body (disorder) HPO C1000483 Genus anemia C0015773 Felty syndrome OrphaNet|MalaCards C0242936 Center pain C0236964 Attention deficit and disruptive behavior disorders HSDN C2911645 Weight loss adverse event C1962986 Glaucoma adverse event HSDN C0020538 Hbp C0342859 Harderoporphyria HPO C1557397 Adverse event associated with pain C0022573 Keratoconjunctivitis HSDN C2911647 Weight gain adverse event C0041374 Tumor virus infections HSDN C0030554 Abnormal sensation C0038587 Substance withdrawal syndrome HSDN C0007758 Cerebellar ataxia C0003873 Rheumatoid arthritis HSDN C0151594 Bloody diarrhea C0220744 Multiple gastrointestinal atresias (disorder) MalaCards C0034933 Abnormal reflexes C0037942 Spinal osteophytosis HSDN C2032396 Pelvic pain on the right C0001580 Adolescent behavior HSDN C0349489 Fetal hypoxia C0000771 Abnormalities, drug induced HSDN C0026826 High muscle tone C0007682 Cns disorder HSDN C0000737 Abdomen pain C0001621 Adrenal gland diseases HSDN C4084775 Usual severity weight loss C1134719 Invasive ductal breast carcinoma HSDN C0497247 Blood pressure elevation C1861456 Stiff skin syndrome MalaCards|HPO C0008031 Pain chest C2984900 Malignant adrenal gland composite pheochromocytoma UMLS C0013362 Dysarthrias C0238265 Encephalopathy, callosal demyelinating HSDN C2984058 Have pain C0014009 Empyema HSDN C0030193 Sense of pain C0037397 Behavior social HSDN C0030552 Paralysis partial C0026598 Movement perception HSDN C0027066 Myoclonic jerking C2937358 Cerebral hemorrhage HSDN C0042798 Vision dim C3537440 Cystinosis, infantile nephropathic MalaCards C0034124 Pupillary disorder C0020302 Hydrophthalmos HSDN C4084774 Have weight loss C0717360 Disease lyme vaccine HSDN C0010520 Skin cyanosis C0020488 Hypernatremia HSDN C0019825 Voice hoarseness C0004030 Aspergillosis HSDN C3463815 Feel fatigue C0475801 Leukemia, prolymphocytic, b-cell HSDN C4084726 Distress cough C0021799 Interprofessional relations HSDN C0036572 Convulsion C3813607 Infantile gastroesophageal reflux HSDN C0557874 Global developmental delay C4014621 Eiee25 MalaCards C4085211 Pain distress question C0015458 Facial hemiatrophy HSDN C1510417 Apraxia of gait C0016065 Polyostotic fibrous dysplasia HSDN C2984057 Have nausea C3495422 Finding relating to sexuality and sexual activity HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0242973 Ventricular dysfunction HSDN C4084776 Weight loss C0020522 Delayed hypersensitivity HSDN C1963066 Joint pain adverse event C0494043 Streptobacillosis MalaCards C0522224 Palsied C0039240 Supraventricular tachycardia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029139 Optical illusion HSDN C3463815 Feel fatigue C0595812 Fistula route HSDN C0271215 Blindness legal C0035344 Retinopathy of prematurity MalaCards|HPO C0030200 Intractable pain C0023448 Lymphoid leukemia HSDN C0312416 Morning sickness C0000768 Congenital abnormality HSDN C4084775 Usual severity weight loss C0042164 Uveitis HSDN C1549543 Administration method - pain C0018133 Graft-vs-host disease HSDN C0002622 Amnesias C0162869 Aneurysm, ruptured HSDN C0039870 Leanness C0206081 Hyperandrogenism HSDN C3829611 Nausea frequency C0020435 Hyperbilirubinemia, hereditary HSDN C1290771 Edema of oral vestibule C1302710 Disorder of body cavity UMLS C3539895 Pelvic pain occurs with bowel movement C0009244 Behavioral cognitive therapy HSDN C0018784 Deafness sensorineural C0340834 Hennekam lymphangiectasia lymphedema syndrome HPO C0018926 Emesis bloody C1963198 Pancreatitis adverse event HSDN C3898969 Have been vomiting C0007099 Carcinoma in situ HSDN C0042963 Symptoms vomiting C1865145 Congenital disorder of glycosylation type 1b MalaCards|HPO|UMLS C1963091 Diarrhea adverse event C0024116 Lung diseases, fungal HSDN C0518090 Frequency of pain question C0013364 Dysautonomia, familial HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018809 Heart neoplasm HSDN C0349588 Stature short C0796121 Primrose syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C1442965 Avascular necrosis of the capital femoral epiphysis MalaCards C1549543 Administration method - pain C0005689 Bladder exstrophy HSDN C4084763 Frequency of shortness of breath C1535939 Pneumocystis jiroveci pneumonia DiseaseOntology|MalaCards C0018808 Murmur C0041207 Truncus arteriosus, persistent HSDN C2024893 Cardiovascular surgery result: fatigue C0035358 Retroperitoneal neoplasm HSDN C4084774 Have weight loss C0154251 Lipid metabolism disorders HSDN C2024893 Cardiovascular surgery result: fatigue C0019097 Hemorrhagic fever, argentinian MalaCards C1549543 Administration method - pain C0038012 Spondylitis HSDN C0860603 Anxiety symptom C0085209 Bovine spongiform encephalitis MalaCards C0011206 Delirium acute C0020538 Hypertensive disease HSDN C0019079 Bloody sputum C0024141 Lupus erythematosus, systemic HSDN C4084769 Vomiting frequency C0018824 Heart valve disease HSDN C0036572 Convulsion C0041466 Typhoid fever HSDN C1557397 Adverse event associated with pain C1532253 Sedentary lifestyle HSDN C1860844 Sparse, thin hair C1848912 Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage MalaCards C0004604 Pain back C0023343 Leprosy HSDN C2984057 Have nausea C0011603 Dermatitis HSDN C4084776 Weight loss C0717360 Disease lyme vaccine HSDN C2984057 Have nausea C0022568 Keratitis HSDN C0426579 Anorexia symptom C0023904 Liver neoplasms, experimental HSDN C4085661 Usual severity nausea C0010823 Cytomegalovirus infections HSDN C0518090 Frequency of pain question C0014457 Eosinophilia HSDN C0030552 Paralysis partial C2984291 Glioblastoma multiforme pathway HSDN C4084725 Usual severity cough C0003507 Aortic valve stenosis HSDN C1963086 Confusion adverse event C1963090 Dehydration adverse event HSDN C1961131 Cough adverse event C0021799 Interprofessional relations HSDN C0010200 Cough symptom C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0700590 Diaphoresis excessive C0432240 Stuve-wiedemann dysplasia OrphaNet|HPO C0234533 Seizure generalized C0751779 Action myoclonus-renal failure syndrome HPO C0850758 Pain pelvic C0010692 Cystitis HSDN C0030552 Paralysis partial C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C1384666 Decreased hearing C0007350 Cat disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001857 Aids related complex HSDN C1549543 Administration method - pain C0020459 Hyperinsulinism HSDN C0019825 Voice hoarseness C0040580 Tracheal diseases HSDN C0271215 Blindness legal C0796074 Mohr-tranebjaerg syndrome MalaCards C0751837 Gait ataxic C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C2919142 Short stature adverse event C1832424 Camera lituania cohen syndrome OrphaNet|MalaCards C0013421 Dystonia C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0413252 Hypothermia due to exposure C0036216 Sarcoma, experimental HSDN C4084775 Usual severity weight loss C0038663 Suicide attempt HSDN C0003862 Pain joint C0524910 Hepatitis c, chronic MalaCards|HSDN C0006370 Bulimia C0017563 Gingival diseases HSDN C1963177 Muscle pain adverse event C1861451 Stormorken syndrome MalaCards C4084802 Usual severity diarrhea C0027813 Neuritis HSDN C4084727 Cough frequency C0859897 Cord dysfunction vocal HSDN C0151786 Weakness muscle C0042373 Vascular diseases HSDN C3815497 Cough C0220847 C hepatitis virus HSDN C0027066 Myoclonic jerking C4078861 Non ketotic hyperglycinemia syndrome MalaCards C0917816 Deficiency mental C0265249 Mietens' syndrome MalaCards C1963281 Vomiting adverse event C0011854 Diabetes mellitus, insulin-dependent HSDN C4084767 Bothered by vomiting C3665596 Warts HSDN C4020887 Photodysphoria C0085859 Polyglandular type i autoimmune syndrome OrphaNet|HPO C0033074 Presbycusis C1963138 Hypertension adverse event HSDN C3463815 Feel fatigue C0015408 Eye injury HSDN C0007859 Pain neck C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0030193 Sense of pain C0037937 Spine injury HSDN C0009676 Confusion state C0920350 Autoimmune thyroiditis HSDN C4085642 Level of joint stiffness C1844887 Catel manzke syndrome OrphaNet|HPO|MalaCards C0013421 Dystonia C1849678 Peroxisomal acyl-coa oxidase deficiency MalaCards|HPO C0476250 Head neck mass C0432363 Shagreen patch UMLS C0242936 Center pain C0008412 Choline deficiency HSDN C0000727 Abdomen acute C0023176 Lead poisoning HSDN C4085210 Usual severity pain C0009021 Clonorchiasis HSDN C0151786 Weakness muscle C0398689 Hyper-igm immunodeficiency syndrome, type 1 HSDN C3887638 Failure to thrive in infant C1846545 Autoimmune lymphoproliferative syndrome type 2b HPO C0019209 Large liver C0036996 Short rib-polydactyly syndrome MalaCards C1963071 Back pain adverse event C0004659 Bacteriuria HSDN C2024878 Cardiovascular surgery result: dyspnea C0032002 Pituitary diseases HSDN C4084766 Vomiting C0014549 Tonic-clonic epilepsy HSDN C0036572 Convulsion C0796004 Kabuki make-up syndrome MalaCards|HPO|UMLS C0027066 Myoclonic jerking C0030569 Secondary parkinson disease HSDN C0013404 Respiratory difficulty C0221348 Hereditary lymphedema and yellow nails OrphaNet|MalaCards C0018524 Hallucinate C1868649 Panic disorder 1 HSDN C4085549 Dizziness C0009404 Colorectal neoplasms HSDN C0015402 Hemorrhage eye C0011311 Dengue fever HSDN C1961131 Cough adverse event C0031090 Periodontal diseases HSDN C0040822 D tremors C0393615 Familial tremor UMLS C2237041 Shox gene with short stature C0042170 Uveomeningoencephalitic syndrome OrphaNet|HPO|MalaCards C0033774 Skin pruritus C0007453 Cattle disease HSDN C2315100 Pediatric failure to thrive C0021843 Intestinal obstruction HSDN C0018772 Deafness C0032584 Polyps HSDN C0030552 Paralysis partial C0559260 Congenital scoliosis HSDN C0036396 Sciatica C0314657 Genetic predisposition HSDN C0030193 Sense of pain C0334548 Juxtacortical chondroma UMLS C0241210 Speaking delay C3281137 Chromosome 17q12 duplication syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0019569 Hirschsprung disease HSDN C0043352 Absent salivary secretion C1443901 Intestinal botulism OrphaNet|MalaCards C4085211 Pain distress question C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0034150 Skin purpura C0079772 T-cell lymphoma HSDN C2237041 Shox gene with short stature C1860786 Down syndrome chromosome region HPO C4084725 Usual severity cough C0022660 Kidney failure, acute HSDN C0042798 Vision dim C2931821 Nakamura osame syndrome MalaCards C2911647 Weight gain adverse event C0242341 Sexual infantilism HSDN C1963091 Diarrhea adverse event C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0003467 Angst C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C2129349 Unreasonable fear of seeing an injury C0349231 Phobic anxiety disorder UMLS C0038868 Supranuclear palsy progressive C0032962 Pregnancy complications HSDN C1279888 Proteinuria of undiagnosed cause C0013504 Echinococcosis, hepatic HSDN C0038002 Spleen enlargement C0085110 Severe combined immunodeficiency MalaCards C1557397 Adverse event associated with pain C0032227 Pleural effusion disorder HSDN C2984058 Have pain C0035455 Rhinitis HSDN C0000737 Abdomen pain C3266898 Waardenburg syndrome OrphaNet|HPO C2024878 Cardiovascular surgery result: dyspnea C0011071 Sudden death HSDN C0013604 Edematous C0003496 Aortic rupture HSDN C4084726 Distress cough C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0000727 Abdomen acute C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0206160 Retic count elevated C1842534 Dystonia 18 (disorder) MalaCards C0522224 Palsied C0015404 Eye infections, bacterial HSDN C0020538 Hbp C0272258 Cryoglobulinemia, primary MalaCards C0013609 Oedema, localised C0151606 Edema labial genital UMLS C3274924 Have been coughing C1962963 Osteoporosis adverse event HSDN C0035078 Failure kidney C1857390 Cystinuria, type a-b HPO C0232462 Appetite decrease C1835664 Tylosis with esophageal cancer MalaCards C1963067 Atrial fibrillation adverse event C3808145 Left ventricular noncompaction 9 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0010418 Cryptosporidiosis HSDN C0007758 Cerebellar ataxia C0270726 Alexander disease OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C1850318 Omodysplasia type 1 MalaCards C4084802 Usual severity diarrhea C1855057 Ataxia-telangiectasia variant v2 HPO C0234146 Absent reflex C4015029 Charcot-marie-tooth disease, recessive intermediate d MalaCards C0002965 Crescendo angina C0014121 Bacterial endocarditis HSDN C0008031 Pain chest C1552262 Nurse practitioner - family HSDN C0002962 Angina C0024232 Lymphatic metastasis HSDN C0007758 Cerebellar ataxia C0243026 Sepsis HSDN C2128208 Elbow soft tissue pain C1862099 Brachydactyly-nystagmus-cerebellar ataxia MalaCards C0476250 Head neck mass C0026686 Cysts salivary UMLS C3539892 Pelvic pain in front C0022661 Kidney failure, chronic HSDN C0030794 Pelvis pain C0042341 Varicocele HSDN C0460137 Push down or depress C0221033 Trisomy x syndrome MalaCards C0007398 Catatonic C0919267 Ovarian neoplasm HSDN C0086439 Activity decreased C0022336 Creutzfeldt-jakob disease HSDN C1384666 Decreased hearing C1852718 Branchiootic syndrome 2 MalaCards C0042798 Vision dim C3665333 Keratitis-ichthyosis-deafness syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0278196 Seizure, startle, partial UMLS C0518090 Frequency of pain question C0007772 Intracranial arteriovenous malformation HSDN C0026603 Motion sickness C1000483 Genus anemia HSDN C0037384 Snore C0005586 Bipolar disorder HSDN C1962972 Proteinuria adverse event C0221032 Familial generalized lipodystrophy MalaCards C4085548 Usual severity dizziness C0023676 Life style HSDN C0040822 D tremors C0009244 Behavioral cognitive therapy HSDN C3827868 Tachycardia by ecg finding C1861848 Paragangliomas 4 MalaCards|HPO C4084784 Diarrhea C0079631 Interdisciplinary communication HSDN C0018808 Murmur C0024586 Malignant carcinoid syndrome MalaCards|HSDN C1963281 Vomiting adverse event C0521585 Gastrointestinal mucositis HSDN C0011168 Disorder deglutition C0341106 Eosinophilic esophagitis OrphaNet|MalaCards C0014591 Bleeding nose C1832942 Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome (disorder) MalaCards|HPO C0581394 Lower extremity swelling C0740728 Lower extremity problem UMLS C0004134 Dyssynergia C0006105 Brain abscess HSDN C0522224 Palsied C0038644 Sudden infant death syndrome HSDN C1135120 Breakthrough pain C0009492 Compartment syndromes HSDN C1962972 Proteinuria adverse event C0043065 Water electrolyte imbalance HSDN C2237041 Shox gene with short stature C1855849 Bartter syndrome, antenatal , type 2 HPO C1279888 Proteinuria of undiagnosed cause C0026470 Monoclonal gammopathy of undetermined significance HSDN C0018772 Deafness C1843232 Deafness, autosomal dominant 52 MalaCards C0151889 Reflexes tendon increased C3539494 Spastic paraplegia 53, autosomal recessive MalaCards C0018524 Hallucinate C0033075 Presbyopia HSDN C0030193 Sense of pain C0018021 Goiter HSDN C4084768 Usual severity vomiting C0006663 Calcinosis HSDN C0241210 Speaking delay C3713418 Ppm-x syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0023827 Liposarcoma HSDN C0262527 Intermittent abdominal pain C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0043097 Perception, weight HSDN C4084769 Vomiting frequency C1706377 Memory device component HSDN C0013362 Dysarthrias C0751877 Hereditary central nervous system demyelinating diseases HSDN C2315100 Pediatric failure to thrive C1859535 Bare lymphocyte syndrome, type ii, complementation group b HPO C0497247 Blood pressure elevation C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards C0557874 Global developmental delay C1866958 Laryngeal and pharyngeal hypoplasia with omphalocele OrphaNet|MalaCards C2032395 Pelvic pain on the left C0302148 Blood clot HSDN C3539890 Pelvic pain causes awakening at night C0012746 Dissociative disorder HSDN C0033377 Caudal displacement C3554079 Combined oxidative phosphorylation deficiency 12 MalaCards C0018784 Deafness sensorineural C0078917 Albinism, ocular HSDN C0857305 Thrombocytopenia purpura C0006309 Brucellosis HSDN C2919142 Short stature adverse event C1860787 Down syndrome critical region HPO C4084776 Weight loss C0017636 Glioblastoma HSDN C4085317 Diarrhea frequency C1963137 Hydrocephalus adverse event HSDN C0018681 Headache, cephalalgia C1336536 Supratentorial glioblastoma UMLS C4084768 Usual severity vomiting C0042384 Vasculitis HSDN C0036572 Convulsion C0751666 Canavan disease, infantile OrphaNet|HPO|MalaCards C2029884 Hearing loss by exam C1962986 Glaucoma adverse event HSDN C4084776 Weight loss C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C0015230 Exanthem C2937267 Rubella with neurological complication UMLS C0086565 Liver function abnormal C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C1969081 Arrhythmogenic right ventricular dysplasia, familial, 12 HPO|UMLS C2911645 Weight loss adverse event C0085423 Gram-negative bacterial infections HSDN C0013421 Dystonia C3553374 Coenzyme q10 deficiency, primary, 5 MalaCards C1963249 Tinnitus adverse event C0752160 Hemangioma, cavernous, central nervous system HSDN C0151908 Dry skin C1850332 Oculotrichodysplasia MalaCards C0917816 Deficiency mental C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C0018524 Hallucinate C2239176 Liver carcinoma HSDN C0860603 Anxiety symptom C2675369 Chromosome 22q11.2 microduplication syndrome HPO C3541349 Syncope C0017181 Gastrointestinal hemorrhage HSDN C0043094 Weight gain C0036117 Salmonella infections HSDN C1963091 Diarrhea adverse event C3810147 Immunodeficiency 19 MalaCards C0917816 Deficiency mental C0043379 Xyy karyotype OrphaNet C4084769 Vomiting frequency C0020428 Hyperaldosteronism HSDN C0033774 Skin pruritus C0553578 Non-bullous ichthyosiform erythroderma MalaCards C4084776 Weight loss C0020456 Hyperglycemia HSDN C0020672 Body temperature decreased C0013080 Down syndrome HSDN C0518090 Frequency of pain question C0019045 Hemoglobinopathies HSDN C3539893 Pelvic pain occurs with intercourse C0004935 Animal ethology HSDN C0015468 Face pain C0015458 Facial hemiatrophy HSDN C3641755 Have constipation C0009376 Colonic polyps HSDN C0013604 Edematous C0020461 Hyperkalemia HSDN C0241137 Skin pallor C0019114 Hemosiderosis HSDN C4050613 Anxiety C4015710 Tenorio syndrome MalaCards C1961131 Cough adverse event C0001721 Emotional affect HSDN C0206146 Myocardial stunning C0242707 Ventricular dysfunction, right HSDN C0085602 Polydypsia C1855681 Nephronophthisis, familial juvenile HPO|UMLS C2984058 Have pain C1270972 Mild cognitive disorder HSDN C4084767 Bothered by vomiting C1963274 Vasculitis adverse event HSDN C3539891 Pelvic pain to the rear C1546602 Specimen source codes - diverticulum HSDN C2315100 Pediatric failure to thrive C1856304 Gsd iv, neuromuscular form, congenital MalaCards|HPO C3541349 Syncope C0023473 Myeloid leukemia, chronic HSDN C0013405 Dyspnea, paroxysmal C1963138 Hypertension adverse event HSDN C0917816 Deficiency mental C3550234 Peroxisome biogenesis disorder 2b MalaCards C4084776 Weight loss C0221204 Lytic lesion HSDN C1549543 Administration method - pain C0030283 Pancreatic cyst HSDN C0151786 Weakness muscle C4225237 Rhizomelic chondrodysplasia punctata, type 5 UMLS C4084784 Diarrhea C0024894 Mastitis HSDN C0012833 Dizzy C0033817 Pseudomonas infections HSDN C3463815 Feel fatigue C0009651 Conditioning operant HSDN C0232503 Bleeding umbilical C0019080 Hemorrhage UMLS C4084768 Usual severity vomiting C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C0006277 Bronchitis C1858266 Bare lymphocyte syndrome, type i MalaCards C0009421 Comatose C0042487 Venous thrombosis HSDN C0039870 Leanness C0030976 Perceptual distortions HSDN C0018681 Headache, cephalalgia C0027627 Neoplasm metastasis HSDN C1961131 Cough adverse event C0878675 Erdheim-chester disease MalaCards C0575081 Abnormal gait C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C0015300 Ocular proptosis C2674876 Loeys dietz syndrome, type 1b HPO C0030193 Sense of pain C0037930 Spinal cord neoplasms HSDN C0024031 Back pain lower back C0024198 Lyme disease HSDN C0426579 Anorexia symptom C0017536 Giardiasis HSDN C2237041 Shox gene with short stature C1851986 Dyschondrosteosis and nephritis OrphaNet|MalaCards C0242936 Center pain C0001427 Adenoiditis, nos MalaCards C2132198 Abnormal blistering of the skin C0024899 Mastocytosis OrphaNet|MalaCards C1579931 Depressed - symptom C2936741 Syndrome xxyy OrphaNet|MalaCards C0423710 Segmental peripheral neuralgia C1527351 Nerve root disorder UMLS C0015672 Decreased energy C0013291 Duodenal neoplasms HSDN C0349588 Stature short C0268345 Ehlers-danlos syndrome, arthrochalasia type OrphaNet|HPO C3274924 Have been coughing C3202971 Non-infective endocarditis HSDN C0019079 Bloody sputum C2347126 Microscopic polyarteritis MalaCards C3541349 Syncope C0033036 Atrial premature complexes HSDN C0002170 Alopecia disorders C0432348 Crandall syndrome OrphaNet|MalaCards C4084724 Usual severity constipation C0085258 Deficiency, yang HSDN C0027796 Neuralgias C0036677 Sensory threshold HSDN C2984058 Have pain C0024959 Maxillary sinusitis HSDN C0086565 Liver function abnormal C2931426 Orofaciodigital syndrome type1 HPO C0557874 Global developmental delay C3150415 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 MalaCards|HPO C0037384 Snore C0004096 Asthma HSDN C4084769 Vomiting frequency C0003496 Aortic rupture HSDN C2237041 Shox gene with short stature C2931291 Familial spastic paraparesis and deafness OrphaNet|MalaCards C0027796 Neuralgias C1534561 (neuralgia/neuritis - nos) or (nerve root pain nec) UMLS C3887638 Failure to thrive in infant C1864997 Majeed syndrome OrphaNet|HPO|MalaCards C0398650 Idiopathic thrombocytopenia purpura C0024314 Lymphoproliferative disorders MalaCards C0242936 Center pain C0000786 Spontaneous abortion HSDN C0013404 Respiratory difficulty C0011265 Presenile dementia HSDN C0032617 High urine output C1865270 Bartter syndrome, type 4a HPO|UMLS C1557397 Adverse event associated with pain C0014848 Esophageal achalasia HSDN C2911645 Weight loss adverse event C1527311 Brain edema HSDN C4085211 Pain distress question C0038644 Sudden infant death syndrome HSDN C3641756 Have diarrhea C0221021 Microangiopathic hemolytic anemia MalaCards C4084774 Have weight loss C0010340 Critical illness HSDN C0413252 Hypothermia due to exposure C2350521 Gustatory perception HSDN C4085211 Pain distress question C0028768 Obsessive-compulsive disorder HSDN C2073927 Choking on liquid C0008301 Choke UMLS C0242936 Center pain C0035042 Psychology and religion HSDN C0030193 Sense of pain C0043202 Wolff-parkinson-white syndrome HSDN C0020673 Hypothermia (central) (local) C0010356 Cross infection HSDN C3146279 Coma C2706915 Language:-:point in time:^patient:- HSDN C0030486 Extremity paralysis, lower C0034067 Pulmonary emphysema HSDN C0036572 Convulsion C0030422 Extra-adrenal paraganglioma HSDN C0012833 Dizzy C0018939 Hematological disease HSDN C4084766 Vomiting C0022423 Judgement HSDN C0002965 Crescendo angina C0023467 Leukemia, myelocytic, acute HSDN C1963281 Vomiting adverse event C1556682 Adverse event associated with infection HSDN C0278152 Hemifacial spasms C0014511 Epithelial cyst HSDN C4084766 Vomiting C0015726 Focused anxiety HSDN C1557397 Adverse event associated with pain C0206663 Neuroectodermal tumor, primitive HSDN C4084723 Constipation C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0042024 Urine incontinence C0003496 Aortic rupture HSDN C0041657 Consciousness loss C0020517 Hypersensitivity HSDN C0034150 Skin purpura C1553188 Hemolysis - observation HSDN C4084776 Weight loss C0003962 Ascites HSDN C3815497 Cough C0020615 Hypoglycemia HSDN C0033774 Skin pruritus C0151744 Myocardial ischemia HSDN C0036572 Convulsion C0016063 Osteitis fibrosa disseminata HSDN C4085317 Diarrhea frequency C0013720 Ehlers-danlos syndrome HSDN C0020673 Hypothermia (central) (local) C0585442 Osteosarcoma of bone HSDN C0036572 Convulsion C0005937 Bone cysts HSDN C0002962 Angina C0030846 Penile diseases HSDN C3539889 Pelvic pain increasing in severity C0302148 Blood clot HSDN C0009676 Confusion state C0014544 Epilepsy HSDN C4084784 Diarrhea C0750394 Wbc low HSDN C4084723 Constipation C0006057 Botulisms OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3463897 Hydatidiform mole, recurrent, 1 HSDN C0009676 Confusion state C0006118 Brain neoplasms HSDN C2911645 Weight loss adverse event C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C0497406 Over weight C0009375 Colonic neoplasms HSDN C0018681 Headache, cephalalgia C0024530 Malaria OrphaNet|HSDN|MalaCards C1963087 Constipation adverse event C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C2024893 Cardiovascular surgery result: fatigue C0005119 Bereavement HSDN C0423823 Nail thinness C1855792 Ichthyosiform erythroderma, congenital, nonbullous, 1 MalaCards|HPO C1263846 Attention deficit disorder with hyperactivity C2675369 Chromosome 22q11.2 microduplication syndrome HPO C2237041 Shox gene with short stature C4015461 Ruijs-aalfs syndrome MalaCards C0242936 Center pain C0001818 Agoraphobia HSDN C1069915 Vertigo C0016542 Foreign body HSDN C1557397 Adverse event associated with pain C0029927 Ovarian cysts HSDN C1963093 Dizziness adverse event C0011854 Diabetes mellitus, insulin-dependent HSDN C0042571 Vertigo subjective C3539923 Cdisc adas-cog - orientation summary score HSDN C0020672 Body temperature decreased C0038525 Subarachnoid hemorrhage HSDN C4084774 Have weight loss C0017150 Gastrinoma OrphaNet|MalaCards C0042928 Paralysis vocal cord C0022665 Kidney neoplasm HSDN C2919142 Short stature adverse event C0265316 Neurocutaneous syndromes MalaCards C1963086 Confusion adverse event C0038525 Subarachnoid hemorrhage HSDN C0023530 Leukopenia C1846142 Hoyeraal-hreidarsson syndrome MalaCards C4084775 Usual severity weight loss C0009062 Clostridia infection HSDN C4085317 Diarrhea frequency C0019372 Herpesviridae infections HSDN C3641756 Have diarrhea C0012147 Dientamoebiases DiseaseOntology C0033774 Skin pruritus C0949506 Porokeratosis of mibelli OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0021368 Inflammation HSDN C0234146 Absent reflex C1836485 Charcot-marie-tooth disease, axonal, type 2a2 (disorder) HPO C0427055 Face weakness C3553625 Facial paresis, hereditary congenital, 3 MalaCards C3887873 Hearing loss C0003090 Ankylosis HSDN C0742305 Chest pain site posterior chest C0026764 Multiple myeloma UMLS C0162285 Edema eyelid C1862259 Blepharoptosis myopia ectopia lentis OrphaNet|MalaCards C1557397 Adverse event associated with pain C0085399 Ehrlichiosis HSDN C4084802 Usual severity diarrhea C0344311 Blister HSDN C0018784 Deafness sensorineural C2678480 Chromosome 22q11.2 deletion syndrome, distal MalaCards|HPO C4085317 Diarrhea frequency C0019326 Ventral hernia HSDN C2169806 Tic C0004364 Autoimmune diseases HSDN C0028738 Nystagmus C2931004 Congenital disorder of glycosylation type 1j MalaCards C0085636 Light sensitivity C0796093 Odontoonychodermal dysplasia MalaCards|HPO C0028961 Urine output decreased C0011581 Depressive disorder HSDN C1963091 Diarrhea adverse event C0011880 Diabetic ketoacidosis HSDN C0036572 Convulsion C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C3898969 Have been vomiting C3888013 Hypnoses HSDN C0042963 Symptoms vomiting C0740392 Infarction, middle cerebral artery HSDN C0234132 Pyramidal sign C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy UMLS C2024893 Cardiovascular surgery result: fatigue C0023055 Laryngeal neoplasm HSDN C2911647 Weight gain adverse event C0014394 Enuresis HSDN C0150055 Pain chronic C0393830 Chron painful diab neuropathy UMLS C4084788 Have dizziness C0010054 Coronary arteriosclerosis HSDN C2911645 Weight loss adverse event C0036467 Scrofula MalaCards C0030193 Sense of pain C0032002 Pituitary diseases HSDN C0151786 Weakness muscle C1963119 Stomach ulcer adverse event HSDN C0013362 Dysarthrias C0685838 Gonadal dysgenesis xx type deafness MalaCards|HPO C4084776 Weight loss C2117118 X-ray of toe: deformity contracture HSDN C0232466 Feeding difficulty C0025517 Metabolic diseases MalaCards C0242936 Center pain C0020877 Ileitis HSDN C0013421 Dystonia C0021295 Infant, premature, diseases HSDN C4084768 Usual severity vomiting C0028758 Bonding HSDN C0011991 Loose stools C0006625 Cachexia HSDN C0018784 Deafness sensorineural C3281192 Infantile cerebellar-retinal degeneration MalaCards C1963071 Back pain adverse event C0302362 Brucella melitensis infection MalaCards C3805026 Anorectal swelling C0854350 Periproctal swelling UMLS C2024893 Cardiovascular surgery result: fatigue C0032002 Pituitary diseases HSDN C1963281 Vomiting adverse event C0494039 Gastrointestinal tularaemia MalaCards C0027497 Queasy C0162651 Gastric outlet obstruction HSDN C0557874 Global developmental delay C0796033 Marden-walker syndrome MalaCards C0018772 Deafness C1853144 Deafness, congenital, with inner ear agenesis, microtia, and microdontia OrphaNet C2911645 Weight loss adverse event C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0022346 Yellow skin C0010034 Corneal diseases HSDN C4085317 Diarrhea frequency C0020557 Hypertriglyceridemia HSDN C0030554 Abnormal sensation C0036677 Sensory threshold HSDN C0019209 Large liver C0206624 Hepatoblastoma MalaCards C0015469 Facial paralysis C0036421 Systemic scleroderma HSDN C0013404 Respiratory difficulty C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO|UMLS C0011991 Loose stools C0085278 Antiphospholipid syndrome HSDN C3641756 Have diarrhea C0015814 Femur head necrosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007137 Squamous cell carcinoma HSDN C2919142 Short stature adverse event C0022716 Menkes kinky hair syndrome MalaCards|HPO C1546759 Specimen source codes - pustule C0406756 Keratolytic winter erythema MalaCards C0460137 Push down or depress C0022336 Creutzfeldt-jakob disease MalaCards|HPO C3146279 Coma C0023055 Laryngeal neoplasm HSDN C0015469 Facial paralysis C0007453 Cattle disease HSDN C0036572 Convulsion C0162316 Iron deficiency anemia HSDN C0851578 Disorder sleep C0024141 Lupus erythematosus, systemic HSDN C0042963 Symptoms vomiting C1837218 Cleft palate, isolated HSDN C0002965 Crescendo angina C0022116 Ischemia HSDN C0344434 Atrial fibrillation ecg C2677338 Cardiomyopathy, dilated, 1aa HPO C0041657 Consciousness loss C0012979 Canine disease HSDN C0030193 Sense of pain C2826601 Duodenal extraskeletal osteosarcoma UMLS C0020672 Body temperature decreased C0023895 Liver diseases HSDN C0040034 Thrombocytopenia C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C0016199 Pain flank C0007130 Mucinous adenocarcinoma HSDN C1963093 Dizziness adverse event C0037305 Neoplasm, skull HSDN C2984058 Have pain C0015670 Child father HSDN C0026838 Spasticity muscle C1856974 Pontocerebellar hypoplasia type 4 (disorder) HPO|UMLS C0030552 Paralysis partial C0270858 Abdominal migraines MalaCards C4049644 Depression C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO C0011206 Delirium acute C0151500 Atropine-like syndrome HSDN C0019209 Large liver C0349499 Fetal cytomegalovirus syndrome OrphaNet|MalaCards C0009792 Consciousness disorder C0475073 Subarachnoid hemorrhage traumatic HSDN C4084727 Cough frequency C3714644 Thymus neoplasms OrphaNet|MalaCards C0042963 Symptoms vomiting C1555914 Psychologist - psychotherapy, group HSDN C0349588 Stature short C0796264 Young-hughes syndrome OrphaNet|MalaCards C0149793 Transient monocular blindness C0751278 Metachromatic leukodystrophy, infant MalaCards C1963170 Hypothermia adverse event C0027412 Opioid-related disorders HSDN C2911645 Weight loss adverse event C0040136 Thyroid neoplasm HSDN C3274924 Have been coughing C0013274 Patent ductus arteriosus HSDN C0424755 Fever symptoms C0002170 Alopecia HSDN C0278152 Hemifacial spasms C0023798 Lipoma HSDN C0426579 Anorexia symptom C0006663 Calcinosis HSDN C0019079 Bloody sputum C1708792 Lymphoepithelioma-like lung carcinoma UMLS C0036572 Convulsion C0024236 Lymphedema HSDN C0042571 Vertigo subjective C1457883 Aggressive reaction HSDN C3641755 Have constipation C0262655 Recurrent urinary tract infection HSDN C4084727 Cough frequency C0034063 Pulmonary edema HSDN C0749870 Upper motor neuron sign C1849722 Polyglucosan body disease, adult form UMLS C0015469 Facial paralysis C0032227 Pleural effusion disorder HSDN C2203646 Jaundice C1547044 Kind of quantity - smell HSDN C0149745 Ulcer mouth C1865370 Severe combined immunodeficiency with sensitivity to ionizing radiation HPO C0011206 Delirium acute C0015695 Fatty liver HSDN C0003862 Pain joint C0009450 Disease caused by microorganism HSDN C0016382 Cutaneous vascular engorgement C0036677 Sensory threshold HSDN C0040034 Thrombocytopenia C1850126 Osteopetrosis, mild autosomal recessive form MalaCards|HPO C0030193 Sense of pain C0013575 Ectodermal dysplasia HSDN C1963135 Hepatic necrosis adverse event C0024620 Primary malignant neoplasm of liver MalaCards C0025287 Meningitis-like C0007820 Cerebrovascular disorders HSDN C0037763 Spasm C1260881 Allergic bronchitis UMLS C1963252 Tremor adverse event C0041408 Turner syndrome HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003469 Anxiety disorders HSDN C0019825 Voice hoarseness C0027651 Tumor HSDN C1963087 Constipation adverse event C0403555 Ochoa syndrome OrphaNet|HPO|MalaCards C0235744 Breath hold C2748910 Rett syndrome, atypical MalaCards C0042928 Paralysis vocal cord C0021432 Infratentorial neoplasms HSDN C4084774 Have weight loss C0700327 Clinical findings relating to memory HSDN C3641756 Have diarrhea C2700553 Omenn syndrome MalaCards C3887638 Failure to thrive in infant C2673610 Jeb-i MalaCards C0019572 Hairiness C1963064 Anxiety adverse event HSDN C1384666 Decreased hearing C1866398 Proteus-like syndrome (disorder) MalaCards|HPO C4084776 Weight loss C0011644 Scleroderma OrphaNet C1565249 Limitation, mobility C0036341 Schizophrenia HSDN C1549543 Administration method - pain C0040592 Trachoma HSDN C0042963 Symptoms vomiting C0473792 Perinatal haematemesis UMLS C4084788 Have dizziness C0042487 Venous thrombosis HSDN C0018808 Murmur C2931643 Madokoro ohdo sonoda syndrome MalaCards C2315100 Pediatric failure to thrive C1850096 Pancreatic agenesis, congenital MalaCards|HPO C0233514 Behavior abnormal C3151411 Mental retardation, autosomal dominant 6 HPO C0042928 Paralysis vocal cord C0004048 Breathing HSDN C3539893 Pelvic pain occurs with intercourse C0016548 Foreign body migration HSDN C2024893 Cardiovascular surgery result: fatigue C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C3463815 Feel fatigue C0475813 Alpha thalassemia-mental retardation syndrome OrphaNet|HPO|MalaCards C3274920 Have shortness of breath question C0008677 Bronchitis, chronic DiseaseOntology|MalaCards C0020450 Hyperemesis gravidarum C0269661 Emesis pregnancy UMLS C1557397 Adverse event associated with pain C1546747 Specimen source codes - polyps HSDN C0413252 Hypothermia due to exposure C0020541 Hypertension, portal HSDN C0004604 Pain back C0007193 Cardiomyopathy, dilated HSDN C2029884 Hearing loss by exam C0037274 Dermatologic disorders HSDN C1557397 Adverse event associated with pain C0020497 Cortical congenital hyperostosis HSDN C0015230 Exanthem C0857089 Dry rash neck UMLS C4085549 Dizziness C0038587 Substance withdrawal syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018206 Granulosa cell tumor HSDN C2700617 Irritation - emotion C0342443 Adrenal cushing's syndrome MalaCards C0151889 Reflexes tendon increased C2931617 Bahemuka brown syndrome MalaCards C0086565 Liver function abnormal C0032749 Post-kala-azar dermal leishmaniasis MalaCards C1069915 Vertigo C0004161 Athletic injuries HSDN C0042024 Urine incontinence C0037315 Sleep apnea syndromes HSDN C4084775 Usual severity weight loss C1527298 Dysentery, bacillary HSDN C0015469 Facial paralysis C2937358 Cerebral hemorrhage HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0205788 Histiocytoid hemangioma HSDN C0018681 Headache, cephalalgia C0034362 Q fever DiseaseOntology|HSDN|MalaCards C2984058 Have pain C0020758 Congenital ichthyosis HSDN C1963071 Back pain adverse event C1997249 Neuralgia, pudendal MalaCards C3665347 Vision impaired C0220658 Pfeiffer syndrome MalaCards C0454644 Delayed language development C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0037763 Spasm C0264423 Asthma, occupational UMLS C3829611 Nausea frequency C0079774 Peripheral t-cell lymphoma HSDN C2242996 Tingling C0037369 Smoking HSDN C1069915 Vertigo C0031117 Peripheral neuropathy HSDN C1971624 Appetite absent C0038160 Staphylococcal infections HSDN C0026826 High muscle tone C0238357 Hyperkalemic periodic paralysis HPO C3815497 Cough C0011265 Presenile dementia HSDN C0015970 Fever unknown origin C0001249 Actinobacillus infections HSDN C0034150 Skin purpura C1258104 Diffuse scleroderma HSDN C0029163 Hemorrhage mouth C0022364 Jaw neoplasms HSDN C4084788 Have dizziness C0348018 Projections HSDN C4084784 Diarrhea C0543514 Glycogen storage disease ixb HPO C0086565 Liver function abnormal C0020557 Hypertriglyceridemia MalaCards C1260880 Nasal drip C1333473 Adenoid cystic carcinoma of ethmoid sinus UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0085409 Polyendocrinopathies, autoimmune HSDN C0424755 Fever symptoms C0043397 Yellow fever, jungle MalaCards C4084766 Vomiting C0024530 Malaria HSDN C0349489 Fetal hypoxia C0012644 Animal disease models HSDN C0037315 Breathing disorder during sleeping C1862941 Amyotrophic lateral sclerosis, sporadic HPO C0018681 Headache, cephalalgia C1333643 Frontal convexity meningioma UMLS C0005779 Clotting C1840365 King denborough syndrome HPO C0022346 Yellow skin C0011581 Depressive disorder HSDN C0746674 Muscle weakness generalized C0025427 Mercury poisoning OrphaNet|MalaCards C0037199 Sinus infection C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C0151740 Intracranial hypertension C0206663 Neuroectodermal tumor, primitive MalaCards C0042963 Symptoms vomiting C0268569 Intermittent maple syrup urine disease HPO C3463815 Feel fatigue C0042338 Herpesvirus 3, human HSDN C0015672 Decreased energy C0010674 Cystic fibrosis HSDN C4085210 Usual severity pain C0241158 Cicatrix skin HSDN C4084724 Usual severity constipation C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4084767 Bothered by vomiting C0002880 Autoimmune hemolytic anemia HSDN C0042963 Symptoms vomiting C2064429 Extrahepatic bile duct adenocarcinoma, intestinal type UMLS C0013362 Dysarthrias C1837092 Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency HPO C0033774 Skin pruritus C2609414 Acute kidney injury HSDN C3887873 Hearing loss C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0497247 Blood pressure elevation C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0017128 Fistula gastric HSDN C0030552 Paralysis partial C0039263 Takayasu arteritis OrphaNet|HSDN|HPO|MalaCards C0002962 Angina C0040997 Trigeminal neuralgia HSDN C0028738 Nystagmus C2931821 Nakamura osame syndrome OrphaNet|HPO|MalaCards C0030552 Paralysis partial C1962963 Osteoporosis adverse event HSDN C4084766 Vomiting C3539923 Cdisc adas-cog - orientation summary score HSDN C0000727 Abdomen acute C0043253 Trauma blunt HSDN C0024031 Back pain lower back C0036117 Salmonella infections HSDN C2024878 Cardiovascular surgery result: dyspnea C0010823 Cytomegalovirus infections HSDN C1579931 Depressed - symptom C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0034933 Abnormal reflexes C0003803 Arnold chiari malformation HSDN C0349489 Fetal hypoxia C1527311 Brain edema HSDN C0033074 Presbycusis C0027651 Tumor HSDN C0576456 Poor feeding C2675527 Myopathy, congenital, compton-north MalaCards C2203646 Jaundice C0013182 Drug allergy HSDN C0237326 Defecation pain C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0522224 Palsied C0008497 Choriocarcinoma HSDN C0018681 Headache, cephalalgia C3897754 Recurrent childhood gemistocytic astrocytoma UMLS C0019572 Hairiness C0010308 Congenital hypothyroidism HSDN C0522224 Palsied C0008625 Chromosome aberrations HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041834 Erythema HSDN C0557874 Global developmental delay C1412397 Ancr gene HPO C0522224 Palsied C0016171 Fistula of intestine, excluding rectum and anus HSDN C0019825 Voice hoarseness C0263666 Dermatomyositis, childhood type MalaCards C0242936 Center pain C0013504 Echinococcosis, hepatic HSDN C0547005 Bleeding mid-cycle C0025874 Metrorrhagia UMLS C0027796 Neuralgias C0026640 Mouth neoplasms HSDN C1384666 Decreased hearing C0155338 Total ophthalmoplegia MalaCards C0022638 Ketosis C1833104 Diabetes mellitus, permanent neonatal MalaCards|HPO C4084775 Usual severity weight loss C0678202 Granulomatous enteritis MalaCards C1963184 Nystagmus adverse event C3554226 Pch7 MalaCards C4085211 Pain distress question C0175702 Williams syndrome HSDN C0024031 Back pain lower back C0021368 Inflammation HSDN C0232466 Feeding difficulty C3493776 Hypothyroidism, congenital, nongoitrous, 1 MalaCards C0231712 Gait waddling C3888088 Smith-mccort dysplasia 1 UMLS C4085210 Usual severity pain C0079772 T-cell lymphoma HSDN C0398650 Idiopathic thrombocytopenia purpura C0268579 Propionic acidemia HSDN C0007859 Pain neck C0009324 Ulcerative colitis HSDN C0520909 Ponv C1956346 Coronary artery disease HSDN C1959630 Eye pain adverse event C0015467 Neuralgia facial HSDN C0013395 Indigestion C1636667 Disorder characterized by eosinophilia HSDN C4084775 Usual severity weight loss C2062326 Eosinophilic enteropathy MalaCards C0000737 Abdomen pain C1333865 Grade 2 rectal adenocarcinoma UMLS C0027497 Queasy C0014175 Endometriosis HSDN C0030552 Paralysis partial C0033817 Pseudomonas infections HSDN C2911647 Weight gain adverse event C2350521 Gustatory perception HSDN C0040822 D tremors C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO|UMLS C4084726 Distress cough C1963064 Anxiety adverse event HSDN C0009421 Comatose C0042769 Virus diseases HSDN C0026821 Cramp C0021308 Infarction HSDN C2911647 Weight gain adverse event C0018939 Hematological disease HSDN C0460137 Push down or depress C0795907 Conotruncal anomaly face syndrome MalaCards C0004604 Pain back C0016045 Fibroma HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0006309 Brucellosis HSDN C3887638 Failure to thrive in infant C0022584 Keratoderma, palmoplantar, diffuse HSDN C1549543 Administration method - pain C0003492 Aortic coarctation HSDN C0033774 Skin pruritus C3273127 Extrahepatic bile duct adenocarcinoma, gastric foveolar type UMLS C0033377 Caudal displacement C0796200 Wieacker-wolff syndrome MalaCards|HPO C0231807 Dyspnea exertional C3812396 Chronic idiopathic pulmonary fibrosis MalaCards C4085210 Usual severity pain C0003950 Ascariasis HSDN C1963184 Nystagmus adverse event C1837206 Cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly HPO C0423713 Ilioinguinal nerve neuralgia C1290866 Disease of pelvis UMLS C0010200 Cough symptom C0015302 External exotoses HSDN C0040822 D tremors C0812393 Cancer patients and suicide and depression HSDN C0522224 Palsied C1306759 Eosinophilic disorder HSDN C0033774 Skin pruritus C0263352 Strophulus UMLS C0917799 Sleeping excessive C2931859 Acquired cjd MalaCards C3539896 Pelvic pain occurs with urination C0269185 Uterus retroverted HSDN C1260880 Nasal drip C2983719 Nasopharyngeal carcinoma by ajcc v6 stage UMLS C0684343 Pseudophakia C0022578 Keratoconus HSDN C0023015 Language handicap C3809483 Sli5 MalaCards C3898969 Have been vomiting C0010674 Cystic fibrosis HSDN C0007758 Cerebellar ataxia C2930815 Acute cerebral gaucher disease MalaCards C0151889 Reflexes tendon increased C3279743 Spastic paraplegia 52, autosomal recessive MalaCards C0518090 Frequency of pain question C0041954 Ureteral diseases and syndromes HSDN C0013378 Dysgensia C0155490 Middle ear cholesteatoma HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0023473 Myeloid leukemia, chronic HSDN C2032396 Pelvic pain on the right C0033038 Ejaculatio praecox HSDN C2203646 Jaundice C0026266 Mitral valve insufficiency HSDN C0027497 Queasy C0524620 Metabolic syndrome x HSDN C0036572 Convulsion C1970203 Polyhydramnios, megalencephaly, and symptomatic epilepsy MalaCards C1145670 Failure respiratory C0342871 Acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0019202 Hepatolenticular degeneration HSDN C2911645 Weight loss adverse event C0007130 Mucinous adenocarcinoma HSDN C0237326 Defecation pain C0342613 Danish type familial amyloid cardiomyopathy MalaCards C3887638 Failure to thrive in infant C0021943 Chromosome inversion HSDN C0497406 Over weight C0042035 Urination disorders HSDN C2315100 Pediatric failure to thrive C1836929 Emanuel syndrome OrphaNet|MalaCards C2169806 Tic C0024906 Masturbation, nos HSDN C4084767 Bothered by vomiting C0079744 Diffuse large b-cell lymphoma HSDN C2203646 Jaundice C0016658 Fracture bone HSDN C0036572 Convulsion C3151781 Ck syndrome MalaCards|HPO C0278152 Hemifacial spasms C0020458 Hyperhidrosis disorder HSDN C1963170 Hypothermia adverse event C0011630 Dermatomycoses HSDN C0022107 Fussiness C0030757 Pediculus capitis infestation DiseaseOntology C0037316 Not enough sleeping C3495422 Finding relating to sexuality and sexual activity HSDN C0030193 Sense of pain C0814263 Meditation therapy HSDN C4084776 Weight loss C0027809 Neurilemmoma HSDN C1961100 Erectile dysfunction adverse event C0206247 Amyloid neuropathies MalaCards C1549543 Administration method - pain C2267227 Bulimia nervosa HSDN C4084768 Usual severity vomiting C0008370 Cholestasis HSDN C0237326 Defecation pain C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0036572 Convulsion C3711125 Mitochondrial dna depletion syndrome 8a MalaCards C1963071 Back pain adverse event C0425045 Sudden infant death HSDN C3898969 Have been vomiting C0021845 Intestinal perforation HSDN C0018681 Headache, cephalalgia C0458220 Nervus intermedius neuralgia MalaCards C1963237 Insomnia adverse event C0024198 Lyme disease MalaCards C0015672 Decreased energy C0008354 Cholera HSDN C0013362 Dysarthrias C0205770 Choroid plexus papilloma HSDN C4085549 Dizziness C1546533 Specimen source codes - abscess HSDN C4084775 Usual severity weight loss C0085073 Prosthesis-related infection HSDN C1963154 Renal failure adverse event C3150874 Cranioectodermal dysplasia 2 MalaCards C0518090 Frequency of pain question C0031526 Philadelphia chromosome HSDN C0026821 Cramp C0010054 Coronary arteriosclerosis HSDN C0011991 Loose stools C0152522 Diarrhea-presumed infectious UMLS C2911645 Weight loss adverse event C0037421 Social isolation HSDN C0023012 Delay language C1853566 Genitopatellar syndrome OrphaNet|HPO|MalaCards C0018777 Deafness, conductive C0024305 Lymphoma, non-hodgkin HSDN C0000737 Abdomen pain C0026946 Mycoses HSDN C3815497 Cough C0015726 Focused anxiety HSDN C4084769 Vomiting frequency C0029132 Disorder of the optic nerve HSDN C0036572 Convulsion C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0018681 Headache, cephalalgia C2875199 Ophthalmoplegic migraine, intractable UMLS C4084897 Sleep disturbance subordinate domain C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C0015672 Decreased energy C0334674 Acute panmyelosis with myelofibrosis UMLS C0494475 Seizure generalized tonic clonic C0270855 Early myoclonic encephalopathy MalaCards C2024878 Cardiovascular surgery result: dyspnea C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C0917816 Deficiency mental C2674949 Chromosome 3q29 deletion syndrome OrphaNet|MalaCards C0085631 Abnormal excitement C0007222 Cardiovascular diseases HSDN C0007758 Cerebellar ataxia C0917796 Optic atrophy, hereditary, leber HSDN|HPO C3887638 Failure to thrive in infant C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0010200 Cough symptom C0029291 Fever, parrot HSDN C4084766 Vomiting C0002514 Amino acid metabolism, inborn errors HSDN C2315100 Pediatric failure to thrive C1850599 Leigh syndrome due to mitochondrial complex iv deficiency HPO C0013595 Eczematous dermatitis C0432443 Deletion of long arm of chromosome 18 MalaCards C0033377 Caudal displacement C0795917 Alpha-thalassemia mental retardation syndrome, deletion-type MalaCards C3641756 Have diarrhea C0311375 Arsenic poisoning HSDN C0019079 Bloody sputum C0032229 Pleural neoplasms HSDN C0012569 Double vision C0009759 Conjunctival diseases HSDN C1384666 Decreased hearing C0005967 Bone neoplasms HSDN C0039070 Collapse fleeting C0024116 Lung diseases, fungal HSDN C0022346 Yellow skin C1881674 Medical device emits smoke HSDN C0007758 Cerebellar ataxia C2931542 Shapiro syndrome OrphaNet|MalaCards C1069915 Vertigo C0025284 Meningeal neoplasms HSDN C3539890 Pelvic pain causes awakening at night C0022661 Kidney failure, chronic HSDN C0162298 Stiffness joints C0035372 Rett syndrome MalaCards|HPO C0027497 Queasy C0014038 Encephalitis HSDN C1000483 Genus anemia C2700553 Omenn syndrome MalaCards|HPO C0030554 Abnormal sensation C1319688 Blister dose form HSDN C0086437 Joint hypermobility C0023003 Langer-giedion syndrome MalaCards C0018932 Bright red rectal bleeding C0220744 Multiple gastrointestinal atresias (disorder) MalaCards|HPO C0030486 Extremity paralysis, lower C3489413 Lipomatosis, multiple HSDN C0030794 Pelvis pain C2350572 Illness behavior HSDN C0271215 Blindness legal C2931205 Usher syndrome, type 1a MalaCards C4084723 Constipation C0026850 Muscular dystrophy HSDN C0151889 Reflexes tendon increased C1857977 Microhydranencephaly MalaCards|HPO C4084775 Usual severity weight loss C1510428 Cerebral abscess HSDN C3146279 Coma C1552527 Clinic / center - developmental disabilities HSDN C0040264 Ear ringing sound C0001418 Adenocarcinoma HSDN C4084802 Usual severity diarrhea C0035334 Retinitis pigmentosa HSDN C2984058 Have pain C0162836 Hidradenitis suppurativa HSDN C3641756 Have diarrhea C0036271 Scalp dermatoses HSDN C0577567 Mass of urogenital structure C0431631 Cyst; embryonal, fallopian tube UMLS C0010520 Skin cyanosis C0001197 Acrodermatitis HSDN C2132198 Abnormal blistering of the skin C0008049 Chicken pox DiseaseOntology|MalaCards C0010200 Cough symptom C1956391 Temporal arteritis MalaCards|HPO C1557397 Adverse event associated with pain C0025958 Microcephaly HSDN C0242936 Center pain C1552262 Nurse practitioner - family HSDN C0232466 Feeding difficulty C1850569 Nemaline myopathy 2 HPO C0040460 Dental pain C0460137 Push down or depress HSDN C0042025 Urinary incontinence stress C0031212 Personality disorders HSDN C4085862 Bothered by nausea C0022758 Kap HSDN C4084767 Bothered by vomiting C4049644 Depression HSDN C3898969 Have been vomiting C1546847 Entity name part type - family HSDN C1963184 Nystagmus adverse event C0022340 Late-infantile neuronal ceroid lipfuscinosis MalaCards C0012833 Dizzy C0155497 Active meniere's-cochlear UMLS C4084727 Cough frequency C2239176 Liver carcinoma HSDN C4085211 Pain distress question C0025303 Meningococcal infections HSDN C0015469 Facial paralysis C0042769 Virus diseases HSDN C1549543 Administration method - pain C0020503 Hyperparathyroidism, secondary HSDN C3829611 Nausea frequency C0206255 Malaria vaccine HSDN C3898969 Have been vomiting C0002736 Amyotrophic lateral sclerosis HSDN C1963252 Tremor adverse event C0314657 Genetic predisposition HSDN C0026821 Cramp C0042075 Urologic diseases HSDN C0018772 Deafness C0019555 Hip dislocation, congenital HSDN C0085632 Listlessness C0338451 Frontotemporal dementia HPO|UMLS C0015230 Exanthem C0302319 Porokeratosis, linear type UMLS C0009421 Comatose C0035305 Retinal detachment HSDN C0235153 Sensory hallucination C0342286 Woodhouse sakati syndrome MalaCards|HPO C1090821 Sepsis C0004364 Autoimmune diseases MalaCards C4085211 Pain distress question C0031526 Philadelphia chromosome HSDN C0018772 Deafness C0043202 Wolff-parkinson-white syndrome HSDN C1557397 Adverse event associated with pain C0020461 Hyperkalemia HSDN C0013604 Edematous C1704421 Skin pigmentation disorder HSDN C0234376 Tremor action C1539956 Tgm6 gene HPO C2237041 Shox gene with short stature C1844375 Gynecomastia, familial MalaCards C3829611 Nausea frequency C0034063 Pulmonary edema HSDN C0040485 Wryneck C0037769 West syndrome HSDN C4042891 Sleep wake disorders C0023269 Leiomyosarcoma HSDN C0518090 Frequency of pain question C0014122 Subacute bacterial endocarditis HSDN C4084774 Have weight loss C0030472 Paraneoplastic syndromes HSDN C0013595 Eczematous dermatitis C1836122 Sarcoidosis, early-onset MalaCards C3641756 Have diarrhea C0848377 Trauma to the abdomen HSDN C4085862 Bothered by nausea C0033968 Psychotherapeutic technique HSDN C0030193 Sense of pain C4039070 Phantom pain following amputation of upper limb UMLS C0028738 Nystagmus C0175695 Sotos' syndrome MalaCards|HPO C4084774 Have weight loss C1510412 Pseudoaneurysm HSDN C0917816 Deficiency mental C0795976 Hirsutism-skeletal dysplasia-mental retardation syndrome OrphaNet|MalaCards C0030193 Sense of pain C0031350 Pharyngitis HSDN C2315100 Pediatric failure to thrive C0019209 Hepatomegaly HSDN C0577572 Mass of musculoskeletal structure C0409787 Villonod.synovitis-upper arm UMLS C0002624 Amnesia retrograde C0497327 Dementia HSDN C3665347 Vision impaired C0917796 Optic atrophy, hereditary, leber HPO C2984057 Have nausea C0085278 Antiphospholipid syndrome HSDN C0018681 Headache, cephalalgia C0014549 Tonic-clonic epilepsy HSDN C0002624 Amnesia retrograde C0270707 Kluver-bucy syndrome HSDN C0037763 Spasm C0161409 Cochlear nerve damage HSDN C0019209 Large liver C0034341 Pyruvate carboxylase deficiency disease MalaCards|HPO C1963071 Back pain adverse event C0027902 Neuropsychological diagnosis HSDN C0015672 Decreased energy C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C0030554 Abnormal sensation C1963067 Atrial fibrillation adverse event HSDN C0241705 Urinary difficulty C1849722 Polyglucosan body disease, adult form UMLS C3665347 Vision impaired C0024215 Lymphangiectasis, intestinal MalaCards C4085549 Dizziness C4050613 Anxiety scale (basc-2) HSDN C0026826 High muscle tone C0265268 Adams oliver syndrome MalaCards|HPO C0010200 Cough symptom C0862792 Stage iiia adenocarcinoma of lung UMLS C0026821 Cramp C1832567 Muscular dystrophy, limb-girdle, type 1c HPO|UMLS C0349588 Stature short C0265565 Congenital pseudoarthrosis of clavicle MalaCards C3274924 Have been coughing C0002874 Aplastic anemia HSDN C1963093 Dizziness adverse event C0039984 Thoracic outlet syndrome HSDN C0027796 Neuralgias C0004623 Bacterial infections HSDN C0038506 Stutter C1999266 Depression adverse event HSDN C0019825 Voice hoarseness C1850627 Keipert syndrome OrphaNet|UMLS|MalaCards C2315100 Pediatric failure to thrive C4048722 Mesoectodermal dysplasia MalaCards C0009806 Constipate C0033770 Prune belly syndrome OrphaNet|HPO|MalaCards C0026826 High muscle tone C0268275 Tay-sachs disease, ab variant HPO C0413252 Hypothermia due to exposure C0040053 Thrombosis HSDN C0043094 Weight gain C0030354 Papilloma HSDN C0151825 Ostalgia C1845168 Hypophosphatemic rickets, x-linked recessive MalaCards|HPO|UMLS C0743973 Fever high C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0036572 Convulsion C0026691 Mucocutaneous lymph node syndrome HSDN C0022346 Yellow skin C0004943 Behcet syndrome HSDN C0030486 Extremity paralysis, lower C0036690 Septicemia HSDN C4084773 Bothered by weight gain C0003493 Aortic diseases HSDN C0026838 Spasticity muscle C0036864 Sexual relations HSDN C1963091 Diarrhea adverse event C0005694 Bladder neck obstruction HSDN C1971624 Appetite absent C0036421 Systemic scleroderma HSDN C0232943 Metromenorrhagia C0025323 Menorrhagia UMLS C1963184 Nystagmus adverse event C1837396 Congenital disorder of glycosylation, type ie MalaCards|HPO C2032395 Pelvic pain on the left C0007621 Neoplastic cell transformation HSDN C0036572 Convulsion C0265210 Weaver syndrome MalaCards|HPO C0011991 Loose stools C1299262 Sarcoma - category (morphologic abnormality) HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004238 Atrial fibrillation HSDN C0149793 Transient monocular blindness C0007786 Brain ischemia HSDN C2984058 Have pain C0014457 Eosinophilia HSDN C0013404 Respiratory difficulty C0022661 Kidney failure, chronic HSDN C0241137 Skin pallor C0342770 Fumarase deficiency MalaCards|HPO C0085631 Abnormal excitement C1556061 Electric injuries HSDN C0021359 Infertility C3151137 Ciliary dyskinesia, primary, 15 MalaCards|HPO C0015676 Mental fatigue C0751774 Nocturnal myoclonus syndrome HSDN C0010200 Cough symptom C0036864 Sexual relations HSDN C4084727 Cough frequency C0020437 Hypercalcemia HSDN C1557397 Adverse event associated with pain C0040559 Toxoplasmosis in animals HSDN C0030193 Sense of pain C0206721 Inverted papilloma HSDN C0013428 Painful urination C0029191 Orchitis HSDN C4085317 Diarrhea frequency C0497580 Condylomata acuminata in men HSDN C0231528 Muscle pain generalized C1836607 Myotilinopathy MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C3714605 Of pain perception HSDN C0018772 Deafness C0003838 Arterial occlusive diseases HSDN C0019825 Voice hoarseness C0035468 Scleroma HSDN C0234146 Absent reflex C1837454 Spinocerebellar ataxia 8 MalaCards C2024893 Cardiovascular surgery result: fatigue C0022104 Irritable bowel syndrome HSDN C0150055 Pain chronic C0002895 Anemia, sickle cell HSDN C0010200 Cough symptom C0004161 Athletic injuries HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C3501853 Long qt syndrome 1-2 MalaCards C2096293 Ent surgical result ear vertigo C0035229 Respiratory insufficiency HSDN C0003962 Ascites C1835664 Tylosis with esophageal cancer MalaCards C4084768 Usual severity vomiting C0920350 Autoimmune thyroiditis HSDN C0008031 Pain chest C2930851 Intestinal lipophagic granulomatosis MalaCards C0040822 D tremors C0035242 Respiratory tract diseases HSDN C4084769 Vomiting frequency C0020502 Hyperparathyroidism HSDN C0231341 Aging premature C1963138 Hypertension adverse event HSDN C2984057 Have nausea C0038160 Staphylococcal infections HSDN C0027498 Nausea vomiting C1847319 Paraganglioma and gastric stromal sarcoma MalaCards C4084774 Have weight loss C3711125 Mitochondrial dna depletion syndrome 8a MalaCards C4084769 Vomiting frequency C1622510 Neurocytoma HSDN C0013404 Respiratory difficulty C0019112 Hemorrhoids HSDN C0557874 Global developmental delay C3553529 Combined oxidative phosphorylation deficiency 10 MalaCards C3203358 Alveolar hypoventilation C3163620 Hypotension adverse event HSDN C0085635 Flash light C0346388 Malignant melanoma of choroid HPO C0040822 D tremors C4014261 Spinocerebellar ataxia, autosomal recessive 16 MalaCards C0018772 Deafness C0796135 Renpenning syndrome 1 HPO C0007758 Cerebellar ataxia C0271270 Oculovestibuloauditory syndrome HSDN C0009792 Consciousness disorder C4084909 Depression subordinate domain HSDN C0917816 Deficiency mental C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards C1279511 Malarial pigment deposition C0406153 Animal-induced dermatosis UMLS C4085317 Diarrhea frequency C0037198 Sinus thrombosis, intracranial HSDN C0020672 Body temperature decreased C0002874 Aplastic anemia HSDN C0018772 Deafness C1412746 Bbs1 gene HPO C3146279 Coma C0008350 Cholelithiasis HSDN C2919142 Short stature adverse event C0553586 Cafe-au-lait macules with pulmonary stenosis OrphaNet|HPO|MalaCards C0497406 Over weight C0018099 Gout HSDN C0033774 Skin pruritus C3873472 Vulvovaginal gingival syndrome MalaCards C4084784 Diarrhea C0014849 Esophageal and gastric varices HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020428 Hyperaldosteronism HSDN C2911645 Weight loss adverse event C0042510 Ventricular fibrillation HSDN C0023015 Language handicap C0001721 Emotional affect HSDN C0577567 Mass of urogenital structure C0034188 Pyelonephritis xanthogranulomatous UMLS C0040822 D tremors C0014070 Encephalomyelitis HSDN C3898969 Have been vomiting C0035801 Diseases rodent HSDN C3539893 Pelvic pain occurs with intercourse C0409354 Flexion contracture of hip HSDN C0032617 High urine output C0037019 Shy-drager syndrome HSDN C0039070 Collapse fleeting C0018188 Granuloma HSDN C0030486 Extremity paralysis, lower C0950124 Papillomavirus infections HSDN C2984057 Have nausea C0021368 Inflammation HSDN C1963137 Hydrocephalus adverse event C0455988 Hydrops fetalis, non-immune MalaCards C2029884 Hearing loss by exam C0003493 Aortic diseases HSDN C0751837 Gait ataxic C4225255 Yuan-harel-lupski syndrome UMLS C0042963 Symptoms vomiting C1509147 Histiocytoma HSDN C0162298 Stiffness joints C0300948 Caudal regression syndrome OrphaNet|HPO C2024893 Cardiovascular surgery result: fatigue C0027404 Narcolepsy HSDN C0036572 Convulsion C0019337 Heroin dependence HSDN C0020673 Hypothermia (central) (local) C0036439 Scoliosis, unspecified HSDN C0233769 Lilliputian hallucination C0018524 Hallucinations UMLS C0038002 Spleen enlargement C0085131 Gangliosidosis gm1 OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0014236 Endophthalmitis HSDN C0031911 Pigment deposition C0027877 Neuronal ceroid-lipofuscinoses MalaCards C2108112 Continuous electrocardiogram ventricular fibrillation C1838527 Long qt syndrome 3, acquired, susceptibility to HPO C1263846 Attention deficit disorder with hyperactivity C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C3280887 Hyperglycinemia, lactic acidosis, and seizures UMLS C2073625 X-ray of chest: pleural effusion C1841989 Glomerulonephritis sparse hair telangiectases MalaCards C2024878 Cardiovascular surgery result: dyspnea C3809192 Pulmonary hypertension, primary, 3 MalaCards C0002962 Angina C0042075 Urologic diseases HSDN C2029884 Hearing loss by exam C0024314 Lymphoproliferative disorders HSDN C2911647 Weight gain adverse event C0029445 Bone necrosis HSDN C0030486 Extremity paralysis, lower C0020097 Htlv-i infections HSDN C0030193 Sense of pain C0428478 Serum triglycerides raised HSDN C0034124 Pupillary disorder C1423541 Vangl2 gene HSDN C1579931 Depressed - symptom C3665349 Secondary hypothyroidism OrphaNet C0002962 Angina C0001173 Adult pyloric stenosis HSDN C3539890 Pelvic pain causes awakening at night C0302148 Blood clot HSDN C0034933 Abnormal reflexes C4085311 Depression - recess HSDN C0018834 Brash C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C2984058 Have pain C0011303 Demyelinating diseases HSDN C0020538 Hbp C0346302 Growth hormone-secreting pituitary adenoma HPO C2984058 Have pain C1509147 Histiocytoma HSDN C0521588 Abnormal jaw movement, nos C1290673 Deflection on mandibular opening UMLS C2237041 Shox gene with short stature C0021368 Inflammation MalaCards C0085631 Abnormal excitement C0220994 Hyperammonemia HSDN C0034124 Pupillary disorder C0042797 Monocular vision HSDN C0018991 Paralysis one side of body C0597109 Nurse's role HSDN C0016204 Fart C0162429 Malnutrition HSDN C0035078 Failure kidney C0403399 Finnish congenital nephrotic syndrome MalaCards|HPO C4085661 Usual severity nausea C0003869 Arthritis, infectious HSDN C0151825 Ostalgia C0022739 Klippel-trenaunay-weber syndrome MalaCards C4085211 Pain distress question C0030470 Paranasal sinus neoplasms HSDN C0043352 Absent salivary secretion C0268381 Primary amyloidosis MalaCards C4084775 Usual severity weight loss C0014118 Endocarditis HSDN C0018834 Brash C0546837 Malignant neoplasm of esophagus OrphaNet|MalaCards C0002965 Crescendo angina C2609414 Acute kidney injury HSDN C4084776 Weight loss C0346407 Pancreatic polypeptide-oma MalaCards C4084774 Have weight loss C0040715 Chromosomal translocation HSDN C0162298 Stiffness joints C0015934 Fetal growth retardation MalaCards C0850758 Pain pelvic C0007621 Neoplastic cell transformation HSDN C0751295 Memory loss or impairment C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C0025287 Meningitis-like C0029291 Fever, parrot HSDN C0009676 Confusion state C1563215 Powassan encephalitis virus infection MalaCards C2911647 Weight gain adverse event C0041318 Tuberculosis, meningeal HSDN C4085211 Pain distress question C2616767 Mycetoma HSDN C0518090 Frequency of pain question C0085271 Self-injurious behavior HSDN C2242996 Tingling C0015467 Neuralgia facial HSDN C4084802 Usual severity diarrhea C0037355 Smallpox vaccines HSDN C0023012 Delay language C0795830 Chromosome 9p deletion syndrome MalaCards C0015469 Facial paralysis C0039496 Temporomandibular joint dysfunction syndrome HSDN C0018681 Headache, cephalalgia C0206526 Tuberculosis, multidrug-resistant HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007784 Cerebral hemisphere hemorrhage HSDN C0009024 Clonus C0270726 Alexander disease OrphaNet|MalaCards C0004134 Dyssynergia C4225364 Myasthenic syndrome, congenital, 18 UMLS C1971624 Appetite absent C0040809 Patient refusal of treatment HSDN C0007859 Pain neck C0009244 Behavioral cognitive therapy HSDN C0043094 Weight gain C0009241 Cognition disorders HSDN C0242936 Center pain C0036982 Shock, hemorrhagic HSDN C2024893 Cardiovascular surgery result: fatigue C0151516 Thyroid hypoplasia OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0026838 Spasticity muscle C1850338 Oculopalatocerebral syndrome MalaCards C1557397 Adverse event associated with pain C0018922 Hemangiopericytoma HSDN C0010038 Corneal opacity disorder C1859782 Aniridia renal agenesis psychomotor retardation OrphaNet|MalaCards C0020458 Hyperhydrosis C0017547 Gigantism OrphaNet C4085222 Nausea C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0038002 Spleen enlargement C1843366 Niemann-pick disease, type c2 MalaCards|HPO C0020673 Hypothermia (central) (local) C0700208 Acquired scoliosis HSDN C1549543 Administration method - pain C0003794 Arm injury HSDN C0009676 Confusion state C0041321 Tuberculosis, miliary HSDN C2132198 Abnormal blistering of the skin C0346104 Follicular atrophoderma and basal cell epitheliomata OrphaNet|MalaCards C4084775 Usual severity weight loss C0343398 Cyclosporiases HSDN C0036572 Convulsion C0276275 Disease due to parvoviridae HSDN C0011168 Disorder deglutition C0345985 Skin neoplasm keratoacanthoma eruptive MalaCards C4084726 Distress cough C0033923 Psychomotor function HSDN C4084784 Diarrhea C0025521 Inborn errors of metabolism HSDN C4085317 Diarrhea frequency C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0037771 Paraparesis spastic C0026709 Mucopolysaccharidosis vi HSDN C2362324 Pediatric obesity C0700327 Clinical findings relating to memory HSDN C0013404 Respiratory difficulty C0021051 Immunologic deficiency syndromes HSDN C4085862 Bothered by nausea C0032269 Pneumococcal infections HSDN C1971624 Appetite absent C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0349588 Stature short C2363065 Vitamin d-resistant rickets OrphaNet|MalaCards C0851578 Disorder sleep C0521168 Injuries occupational HSDN C4084775 Usual severity weight loss C0020502 Hyperparathyroidism HSDN C0007758 Cerebellar ataxia C1864112 Huntington disease-like 1 MalaCards C4085642 Level of joint stiffness C1849929 Pfeiffer palm teller syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0700327 Clinical findings relating to memory HSDN C0013604 Edematous C0032320 Peritoneal free air HSDN C4084769 Vomiting frequency C0004933 Behavior modification technique HSDN C4084784 Diarrhea C0036875 Disorders of sex development HSDN C1963091 Diarrhea adverse event C0162565 Acute intermittent porphyria MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0027095 Myosarcoma HSDN C1069915 Vertigo C1832600 Naxos disease OrphaNet|HPO|MalaCards C0027498 Nausea vomiting C0343068 Familial cold urticaria OrphaNet|HPO|MalaCards C0030193 Sense of pain C0346017 Adenoid cystic carcinoma of skin UMLS C0018784 Deafness sensorineural C0424688 Small head HSDN C3274924 Have been coughing C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C1090821 Sepsis C0001768 Agammaglobulinemia MalaCards C0043094 Weight gain C0020541 Hypertension, portal HSDN C1384666 Decreased hearing C0021355 Infective otitis externa HSDN C0020639 Hypoproteinaemia C2700553 Omenn syndrome MalaCards C0455988 Hydrops fetalis non immune C1843004 Hypotrichosis-lymphedema-telangiectasia syndrome MalaCards|HPO C0036572 Convulsion C0422850 Seizure, somatosensory UMLS C4085862 Bothered by nausea C0029443 Osteomyelitis HSDN C0004941 Behavioral symptoms C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C0497247 Blood pressure elevation C0751202 Cystathionine beta-synthase deficiency disease OrphaNet|HPO C2984057 Have nausea C0034063 Pulmonary edema HSDN C2911647 Weight gain adverse event C0027686 Pathologic neovascularization HSDN C2024893 Cardiovascular surgery result: fatigue C0039978 Thoracic diseases HSDN C0240715 Perineal lump C1827434 Stage i seminoma UMLS C0151603 Edema generalized C2239176 Liver carcinoma MalaCards C0004604 Pain back C2711227 Steatohepatitis HSDN C0018989 Paresis of one side of body C0349604 Intracranial meningioma MalaCards C1963087 Constipation adverse event C0002940 Aneurysm HSDN C0850758 Pain pelvic C1961100 Erectile dysfunction adverse event HSDN C2024893 Cardiovascular surgery result: fatigue C0043325 Xanthomatosis HSDN C4084784 Diarrhea C1970820 Fabry disease, cardiac variant HPO C0042024 Urine incontinence C0007130 Mucinous adenocarcinoma HSDN C0018784 Deafness sensorineural C0079744 Diffuse large b-cell lymphoma HSDN C2237041 Shox gene with short stature C1864445 Histiocytosis with joint contractures and sensorineural deafness MalaCards|HPO C4085211 Pain distress question C0085271 Self-injurious behavior HSDN C0026838 Spasticity muscle C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2364111 Gustatory anesthesia C0027859 Acoustic neuroma HSDN C3641755 Have constipation C0005686 Urinary bladder diseases HSDN C0036572 Convulsion C0009443 Common cold HSDN C0522224 Palsied C0024636 Malocclusion HSDN C4084727 Cough frequency C0015230 Exanthema HSDN C1962972 Proteinuria adverse event C0019829 Hodgkin disease HSDN C0424755 Fever symptoms C1857301 Dermatoosteolysis kirghizian type OrphaNet|MalaCards C1961131 Cough adverse event C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0018772 Deafness C0009450 Disease caused by microorganism HSDN C3887638 Failure to thrive in infant C1850406 Navajo neurohepatopathy MalaCards|HPO C0086565 Liver function abnormal C3281234 Combined oxidative phosphorylation deficiency 9 MalaCards C1963167 Memory impairment adverse event C1843015 Alzheimer disease, familial, 3, with spastic paraparesis and apraxia HPO C0030193 Sense of pain C0085396 Neisseriaceae infections HSDN C1963093 Dizziness adverse event C0017658 Glomerulonephritis HSDN C0020458 Hyperhydrosis C0221055 Paramyotonia congenita (disorder) MalaCards C4085548 Usual severity dizziness C0018671 Head and neck neoplasms HSDN C0018784 Deafness sensorineural C2931176 Familial progressive vestibulo-cochlear dysfunction OrphaNet|MalaCards C3539896 Pelvic pain occurs with urination C0796561 Melanoma vaccines HSDN C0015672 Decreased energy C0018916 Hemangioma HSDN C0027498 Nausea vomiting C2713447 Hyperpotassemia and hypertension, familial MalaCards C0030193 Sense of pain C0007771 Intracranial arteriosclerosis HSDN C0013390 Cramps menstrual C0018801 Heart failure HSDN C4084766 Vomiting C0010481 Cushing syndrome HSDN C2228141 Secondary diurnal enuresis C0270328 Diurnal enuresis UMLS C1579931 Depressed - symptom C2936346 22q11 deletion syndrome MalaCards C0040822 D tremors C0027746 Nerve degeneration HSDN C0011991 Loose stools C0025061 Disease of mediastinum HSDN C4084776 Weight loss C4050613 Anxiety scale (basc-2) HSDN C0042571 Vertigo subjective C0005424 Biliary tract diseases HSDN C0039070 Collapse fleeting C1546635 Specimen source codes - fistula HSDN C1557397 Adverse event associated with pain C0012813 Diverticulitis HSDN C0042963 Symptoms vomiting C0019100 Severe dengue HSDN C4084769 Vomiting frequency C0016483 Food preferences HSDN C0151786 Weakness muscle C0002878 Anemia, hemolytic HSDN C4084784 Diarrhea C1283620 Sucrase-isomaltase deficiency, congenital OrphaNet|HPO|MalaCards C2984058 Have pain C0042076 Urologic neoplasms HSDN C0018681 Headache, cephalalgia C0268386 Amyloid polyneuropathy, swiss type MalaCards C0349588 Stature short C1853576 Diamond-blackfan anemia with microtia and cleft palate HPO C1963071 Back pain adverse event C0015457 Expression facial HSDN C0085631 Abnormal excitement C0030305 Pancreatitis HSDN C4084802 Usual severity diarrhea C1865370 Severe combined immunodeficiency with sensitivity to ionizing radiation HPO C0001825 Agraphia C0017638 Glioma HSDN C2096293 Ent surgical result ear vertigo C0271375 Cranial nerve palsy iv trochlear HSDN C0241137 Skin pallor C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C0036572 Convulsion C0040558 Toxoplasmosis HSDN C0034150 Skin purpura C0000833 Abscess HSDN C4084767 Bothered by vomiting C0032131 Plasmacytoma HSDN C0040485 Wryneck C4050613 Anxiety scale (basc-2) HSDN C2024893 Cardiovascular surgery result: fatigue C1547046 Kind of quantity - taste HSDN C1549543 Administration method - pain C0004940 Behavioral science HSDN C0242936 Center pain C0032320 Peritoneal free air HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016659 Close fracture HSDN C4085210 Usual severity pain C0030469 Paranasal sinus diseases HSDN C0151786 Weakness muscle C0042075 Urologic diseases HSDN C0026838 Spasticity muscle C0023343 Leprosy HSDN C0007859 Pain neck C0521542 Brainstem infarct HSDN C0002962 Angina C2937287 Hematolysis HSDN C1384606 Dyspareunia C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C2937225 Biotin deficiency disease MalaCards C2984057 Have nausea C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0002622 Amnesias C0003624 Appetitive behavior HSDN C4084773 Bothered by weight gain C0020459 Hyperinsulinism HSDN C0012833 Dizzy C0039082 Syndrome HSDN C0349506 Sun sensitivity C0580181 Benign lymphocytic infiltration of jessner OrphaNet C0575081 Abnormal gait C0751587 Cadasil syndrome OrphaNet|HPO C0027497 Queasy C0008924 Cleft lip HSDN C0020455 Hypergammaglobulinemia C0011849 Diabetes mellitus HSDN C0015672 Decreased energy C0859942 Hanot's cirrhosis MalaCards|HPO C1535893 Orthostatic intolerance C0026127 Military psychiatry HSDN C0036572 Convulsion C1866174 Phosphoglycerate dehydrogenase deficiency MalaCards|HPO|UMLS C0031911 Pigment deposition C2931038 Pancreatic carcinoma, familial MalaCards C0019572 Hairiness C0020538 Hypertensive disease HSDN C0019521 Hiccoughs C0013124 Behavior drinking HSDN C0042928 Paralysis vocal cord C0034885 Rectal neoplasms HSDN C0007758 Cerebellar ataxia C0043251 Wounds and injuries HSDN C0549248 Electric sensations shock C0030554 Paresthesia UMLS C0013604 Edematous C0022729 Klebsiella infections HSDN C0013421 Dystonia C1970270 Choreoathetosis and congenital hypothyroidism HPO C4085211 Pain distress question C0005830 Blood protein disorders HSDN C0000737 Abdomen pain C0151824 Colic biliary UMLS C0013390 Cramps menstrual C1458155 Mammary neoplasms HSDN C0019079 Bloody sputum C0032963 Pregnancy complications, cardiovascular HSDN C0027066 Myoclonic jerking C1855008 Mitochondrial complex ii deficiency MalaCards|HPO|UMLS C1963252 Tremor adverse event C0001418 Adenocarcinoma HSDN C1963091 Diarrhea adverse event C0003650 Apudoma HSDN C0011991 Loose stools C0030489 Paraproteinemias HSDN C0242936 Center pain C0162871 Aortic aneurysm, abdominal HSDN C0027066 Myoclonic jerking C0000768 Congenital abnormality HSDN C3665492 Pigmentations C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0023012 Delay language C2673874 Bardet biedl syndrome 14 (disorder) HPO C2984058 Have pain C0006114 Cerebral edema HSDN C0009421 Comatose C0302148 Blood clot HSDN C0007758 Cerebellar ataxia C0026782 Mumps vaccine HSDN C0349588 Stature short C2931622 Ring chromosome 7 OrphaNet|MalaCards C0344435 Ventricular fibrillation by ecg finding C2748541 Brugada syndrome 5 MalaCards|HPO C0027424 Congestion nasal C1852502 Craniometaphyseal dysplasia, autosomal dominant HPO C0002622 Amnesias C0039841 Thiamine deficiency HSDN C3541349 Syncope C0919267 Ovarian neoplasm HSDN C1549543 Administration method - pain C0006736 Body stone HSDN C0013604 Edematous C0023055 Laryngeal neoplasm HSDN C4084802 Usual severity diarrhea C0026865 Mushroom poisoning HSDN C1557397 Adverse event associated with pain C0007771 Intracranial arteriosclerosis HSDN C4085317 Diarrhea frequency C0020461 Hyperkalemia HSDN C2237041 Shox gene with short stature C3150910 Rajab syndrome MalaCards C0027497 Queasy C0026857 Musculoskeletal diseases HSDN C3539896 Pelvic pain occurs with urination C0033873 Psychiatry HSDN C0577564 Mass of lymphoreticular structure C0348396 Unsp b-cell non-hodg lympha UMLS C0542476 Forgetful C0751587 Cadasil syndrome OrphaNet|HPO C4084726 Distress cough C0018801 Heart failure HSDN C0000737 Abdomen pain C0281508 Desmoplastic small round cell tumor OrphaNet|HPO|MalaCards C1963184 Nystagmus adverse event C0549567 Pigmentation disorders MalaCards C0043352 Absent salivary secretion C0282207 Cronkhite-canada syndrome MalaCards C0020580 Decreased sensation C0010054 Coronary arteriosclerosis HSDN C4084726 Distress cough C0019655 Histoplasmosis HSDN C4085211 Pain distress question C0010631 Cystadenocarcinoma HSDN C0242936 Center pain C0016667 Fragile x syndrome HSDN C1549543 Administration method - pain C0003125 Anorexia nervosa HSDN C0030193 Sense of pain C0037928 Spinal cord diseases HSDN C1549543 Administration method - pain C0206704 Carcinoma, large cell HSDN C0036572 Convulsion C0393677 Benign occipital epilepsy of childhood - late onset variant UMLS C3539895 Pelvic pain occurs with bowel movement C0041311 Tuberculosis, female genital HSDN C2237041 Shox gene with short stature C3469606 Pseudohypoaldosteronism, type iie MalaCards C4084726 Distress cough C1836929 Emanuel syndrome MalaCards C0242936 Center pain C0029118 Opportunistic infections HSDN C2919142 Short stature adverse event C2678036 Craniofacioskeletal syndrome MalaCards C3539896 Pelvic pain occurs with urination C0010692 Cystitis HSDN C1963274 Vasculitis adverse event C2973529 Leukocytoclastic vasculitis MalaCards C0020538 Hbp C0543697 Mixed cryoglobulinemia MalaCards C0040460 Dental pain C0040427 Tooth abnormalities HSDN C3641756 Have diarrhea C0000744 Abetalipoproteinemia HSDN C4084725 Usual severity cough C0796561 Melanoma vaccines HSDN C4084773 Bothered by weight gain C0042580 Vesico-ureteral reflux HSDN C1963091 Diarrhea adverse event C0015461 Facial neoplasms HSDN C0040485 Wryneck C2231322 Right-sided ocular torticollis UMLS C4084773 Bothered by weight gain C0019196 Hepatitis c HSDN C0349588 Stature short C0033788 Pseudo-hurler polydystrophy OrphaNet|HPO|MalaCards C0028738 Nystagmus C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0917816 Deficiency mental C2931835 Hyperprolinemia type 2 MalaCards C0018772 Deafness C0011175 Dehydration HSDN C0023012 Delay language C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C4084768 Usual severity vomiting C0013514 Echinostomiasis DiseaseOntology C0030552 Paralysis partial C0040558 Toxoplasmosis HSDN C0018681 Headache, cephalalgia C0033054 Prenatal exposure delayed effects HSDN C0020672 Body temperature decreased C0038587 Substance withdrawal syndrome HSDN C4042891 Sleep wake disorders C0546983 Post-concussion syndrome HSDN C1384666 Decreased hearing C0270911 Charcot-marie-tooth disease, type ia (disorder) HPO C2911647 Weight gain adverse event C1548777 Specimen reject reason - hemolysis HSDN C0151786 Weakness muscle C0015745 Ingestive behavior HSDN C2315100 Pediatric failure to thrive C2931642 Benign symmetrical lipomatosis HSDN C0332573 Macula C0263342 Urticaria pigmentosa, maculopapular type UMLS C4085210 Usual severity pain C0003794 Arm injury HSDN C0041667 Low weight C0033300 Progeria OrphaNet C0036572 Convulsion C4039786 Status epilepticus due to intractable complex partial seizures UMLS C0013604 Edematous C0015934 Fetal growth retardation HSDN C2237041 Shox gene with short stature C3809853 Mental retardation, autosomal recessive 39 MalaCards C0274369 Pain due to any device, implant or graft C2368393 Pain due to cardiac device, implant, or graft UMLS C0242936 Center pain C0236664 Alcohol-related disorders HSDN C1384666 Decreased hearing C0432272 Van buchem disease MalaCards|HPO C0221232 Welts C1304201 Angio-oedema of tongue UMLS C0011168 Disorder deglutition C0038325 Stevens-johnson syndrome OrphaNet|HPO C3898969 Have been vomiting C0340629 Aortic aneurysm without mention of rupture nos HSDN C0151889 Reflexes tendon increased C2750537 Myopathy, actin, congenital, with cores HPO C0036572 Convulsion C0010414 Infection by cryptococcus neoformans HSDN C0242936 Center pain C1527336 Sjogren's syndrome HSDN C4084776 Weight loss C0010692 Cystitis HSDN C2919142 Short stature adverse event C1428293 Slx4 gene HPO C2029884 Hearing loss by exam C0011265 Presenile dementia HSDN C0019521 Hiccoughs C0011581 Depressive disorder HSDN C0041657 Consciousness loss C0004096 Asthma HSDN C0016199 Pain flank C0042035 Urination disorders HSDN C4084784 Diarrhea C0022890 Labyrinthine disorder HSDN C0271215 Blindness legal C0338078 Non-functioning pituitary gland neoplasm MalaCards C0004134 Dyssynergia C4015261 Polyendocrine-polyneuropathy syndrome MalaCards|UMLS C0002962 Angina C0524909 Hepatitis b, chronic HSDN C1962976 Ventricular fibrillation adverse event C1865019 Short qt syndrome 2 (disorder) MalaCards C0026603 Motion sickness C0011849 Diabetes mellitus HSDN C1963086 Confusion adverse event C0007453 Cattle disease HSDN C4084726 Distress cough C0236969 Substance-related disorders HSDN C0221232 Welts C0263336 Immunologic urticaria UMLS C4085211 Pain distress question C0015328 Behavior, exploratory HSDN C4085211 Pain distress question C0043241 Wound infection HSDN C0030193 Sense of pain C0043395 Yellow fever HSDN C0015970 Fever unknown origin C0040156 Thyrotoxicosis HSDN C0027497 Queasy C2981668 Stage iii distal bile duct cancer UMLS C4084774 Have weight loss C0018800 Cardiomegaly HSDN C0015300 Ocular proptosis C0796232 Bohring syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0011586 Three dimensional vision HSDN C1963091 Diarrhea adverse event C1963211 Pericarditis adverse event HSDN C0406671 Burning scrotum C1290026 Disease of skin and/or subcutaneous tissue of trunk UMLS C0878709 Cloudy (hemodialysis) (peritoneal) dialysis effluent C0022661 Kidney failure, chronic UMLS C1962972 Proteinuria adverse event C0023195 Lecithin acyltransferase deficiency OrphaNet|HPO C4084788 Have dizziness C0013370 Amebic colitis HSDN C0040264 Ear ringing sound C0010674 Cystic fibrosis HSDN C1963281 Vomiting adverse event C1962983 Cataract adverse event HSDN C0010520 Skin cyanosis C0023903 Liver neoplasms HSDN C2911647 Weight gain adverse event C0004144 Atelectasis HSDN C0018991 Paralysis one side of body C0033586 Failure, prosthesis HSDN C0004093 Asthenia C0024205 Lymphadenitis HSDN C0424755 Fever symptoms C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C4085222 Nausea C0030568 Parkinsonism, postencephalitic HSDN C0013421 Dystonia C0024586 Malignant carcinoid syndrome HSDN C0011991 Loose stools C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C0037036 Increased salivation C0034494 Rabies (disorder) OrphaNet|MalaCards C0013604 Edematous C0035923 German measles vaccine HSDN C1384666 Decreased hearing C0025958 Microcephaly HSDN C2237041 Shox gene with short stature C1838299 Peroxisome biogenesis disorder, complementation group 14 MalaCards C0013395 Indigestion C0003469 Anxiety disorders HSDN C4084776 Weight loss C0036690 Septicemia HSDN C4084784 Diarrhea C0014859 Esophageal neoplasms HSDN C0024031 Back pain lower back C0023467 Leukemia, myelocytic, acute HSDN C0013394 Coitus painful C1334818 Multicystic mesothelioma of peritoneum MalaCards C1963087 Constipation adverse event C0520946 Emotional hypersensitivity HSDN C1963170 Hypothermia adverse event C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0518090 Frequency of pain question C1962958 Hematoma adverse event HSDN C0917816 Deficiency mental C0206115 Wagr syndrome OrphaNet|HPO C0036659 Sensation disorder C0004153 Atherosclerosis HSDN C0003469 Anxiety disorder C1970035 Parkinson disease 6, late-onset, susceptibility to HPO C0242936 Center pain C0017572 Gingival recession HSDN C0042963 Symptoms vomiting C0041956 Ureteral obstruction HSDN C4085317 Diarrhea frequency C0042514 Tachycardia, ventricular HSDN C0518090 Frequency of pain question C0003496 Aortic rupture HSDN C4084774 Have weight loss C0038362 Stomatitis HSDN C4084768 Usual severity vomiting C0007124 Noninfiltrating intraductal carcinoma HSDN C4084768 Usual severity vomiting C0033923 Psychomotor function HSDN C3463815 Feel fatigue C0018798 Congenital heart defects HSDN C3146279 Coma C0033968 Psychotherapeutic technique HSDN C0005745 Blepharoptosis C1836460 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 MalaCards|HPO C4084776 Weight loss C0206615 Diseases due to pneumovirus HSDN C0035229 Respiratory function impaired C3809971 Asparagine synthetase deficiency MalaCards C0030975 Disorders perception C0004114 Astrocytoma HSDN C0024031 Back pain lower back C0024115 Lung diseases HSDN C1963065 Apnea adverse event C0302148 Blood clot HSDN C0413252 Hypothermia due to exposure C4050613 Anxiety scale (basc-2) HSDN C0013421 Dystonia C0017083 Gangliosidoses MalaCards C4084774 Have weight loss C0042514 Tachycardia, ventricular HSDN C4084767 Bothered by vomiting C1509147 Histiocytoma HSDN C4084767 Bothered by vomiting C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C1838869 Proximal neurogenic muscle weakness C0410214 Myopathy with abnormal lipid metabolism HPO C4084773 Bothered by weight gain C0040997 Trigeminal neuralgia HSDN C4085211 Pain distress question C0011071 Sudden death HSDN C2911645 Weight loss adverse event C1547940 Specimen source codes - ulcer HSDN C3887873 Hearing loss C0009395 Color perception HSDN C0032617 High urine output C2751312 Bartter syndrome, type 4b HPO|UMLS C1963281 Vomiting adverse event C3888013 Hypnoses HSDN C0018784 Deafness sensorineural C1368355 Synostosis malformation HSDN C1384666 Decreased hearing C0024761 Communication, manual HSDN C1549543 Administration method - pain C0039236 Tachycardia episodic HSDN C0237326 Defecation pain C0795841 Jacobsen distal 11q deletion syndrome OrphaNet|HPO|MalaCards C1279888 Proteinuria of undiagnosed cause C0037928 Spinal cord diseases HSDN C2315100 Pediatric failure to thrive C0032797 Postpartum hemorrhage HSDN C0020305 Fetal edema C0026499 Monosomy HSDN C0011991 Loose stools C0037999 Splenic neoplasms HSDN C3274924 Have been coughing C1266101 Thymic epithelial tumor OrphaNet C0018834 Brash C1855101 Methylmalonyl-coa epimerase deficiency with sepiapterin reductase deficiency HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0021400 Influenza HSDN C0037315 Breathing disorder during sleeping C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0040822 D tremors C1853578 Neuroferritinopathy MalaCards|HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0018133 Graft-vs-host disease HSDN C0043094 Weight gain C0524851 Neurodegenerative disorders HSDN C0518090 Frequency of pain question C0015328 Behavior, exploratory HSDN C0242936 Center pain C0016659 Close fracture HSDN C0020615 Hypoglycemia nos C0022716 Menkes kinky hair syndrome MalaCards|HPO C0009676 Confusion state C0700327 Clinical findings relating to memory HSDN C3203358 Alveolar hypoventilation C0080040 Polio post syndrome MalaCards C2911645 Weight loss adverse event C0042900 Vitiligo HSDN C0003862 Pain joint C0018799 Heart diseases HSDN C3539893 Pelvic pain occurs with intercourse C0018799 Heart diseases HSDN C0015469 Facial paralysis C0007350 Cat disease HSDN C0522224 Palsied C0035869 Rotavirus infections HSDN C2984058 Have pain C0751931 Femoral lesion nerve HSDN C3887638 Failure to thrive in infant C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C2203646 Jaundice C0004161 Athletic injuries HSDN C0037763 Spasm C0266143 Cardiospasm; congenital UMLS C0851578 Disorder sleep C0007350 Cat disease HSDN C3539023 Pelvic pain increasing in frequency C0040053 Thrombosis HSDN C2984058 Have pain C0035459 Atrophic rhinitis HSDN C0349588 Stature short C1857977 Microhydranencephaly MalaCards|HPO C2700617 Irritation - emotion C0020497 Cortical congenital hyperostosis DiseaseOntology|MalaCards C1963252 Tremor adverse event C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards C0036572 Convulsion C0022876 Premature obstetric labor HSDN C0242936 Center pain C0376378 Barre lieou syndrome HSDN C0023380 Lethargy C0024788 Green monkey virus disease MalaCards C2029884 Hearing loss by exam C3714514 Infection HSDN C0038868 Supranuclear palsy progressive C1963138 Hypertension adverse event HSDN C0002965 Crescendo angina C1999266 Depression adverse event HSDN C0518090 Frequency of pain question C0085209 Bovine spongiform encephalitis HSDN C4084724 Usual severity constipation C0018916 Hemangioma HSDN C0851578 Disorder sleep C0040809 Patient refusal of treatment HSDN C4084776 Weight loss C0004030 Aspergillosis HSDN C0857305 Thrombocytopenia purpura C0006147 Breast fed HSDN C0024031 Back pain lower back C0025063 Mediastinal neoplasms HSDN C4084727 Cough frequency C1299262 Sarcoma - category (morphologic abnormality) HSDN C0851578 Disorder sleep C0032343 Poisoning HSDN C2029884 Hearing loss by exam C4049644 Depression HSDN C0042798 Vision dim C0024299 Lymphoma HSDN C4084802 Usual severity diarrhea C0027660 Neoplasms, glandular and epithelial HSDN C0016382 Cutaneous vascular engorgement C0006845 Candidiasis, chronic mucocutaneous OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0032064 Plague HSDN C0040822 D tremors C0032787 Postoperative complications HSDN C1549543 Administration method - pain C0013370 Amebic colitis HSDN C0043094 Weight gain C0079631 Interdisciplinary communication HSDN C3829611 Nausea frequency C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0030193 Sense of pain C0234247 Atypical neuralgia UMLS C0018784 Deafness sensorineural C0029877 Ear inflammation HSDN C4084769 Vomiting frequency C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C0009421 Comatose C0040046 Thrombophlebitis HSDN C0026838 Spasticity muscle C0751967 Multiple sclerosis, relapsing-remitting HSDN C0004093 Asthenia C0033927 Psychopathology HSDN C0020649 Blood pressure decreased C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C1963071 Back pain adverse event C0032285 Pneumonia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1532560 Plasmacytoma - category HSDN C0030193 Sense of pain C0013100 Dracontiasis HSDN C0010200 Cough symptom C0001969 Alcoholic intoxication HSDN C0700590 Diaphoresis excessive C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0036572 Convulsion C0270858 Abdominal migraines MalaCards C3539890 Pelvic pain causes awakening at night C0020517 Hypersensitivity HSDN C0040822 D tremors C0520946 Emotional hypersensitivity HSDN C0575081 Abnormal gait C2931826 Potassium aggravated myotonia OrphaNet C1963077 Bone pain adverse event C0014084 Enchondromatosis OrphaNet|HPO|MalaCards C0041834 Erythematous condition C0014804 Erythromelalgia OrphaNet|HPO|MalaCards C0018772 Deafness C0004943 Behcet syndrome HSDN C2919142 Short stature adverse event C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0002170 Alopecia HSDN C0033377 Caudal displacement C0265338 Coffin-siris syndrome HPO C0917816 Deficiency mental C2931402 Lubani al saleh teebi syndrome OrphaNet|MalaCards C0221166 Paraparesis C0027663 Neoplasms, multiple primary HSDN C1963137 Hydrocephalus adverse event C0019562 Von hippel-lindau syndrome OrphaNet|HPO|MalaCards C0086437 Joint hypermobility C1845861 Mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait HPO|UMLS C0011206 Delirium acute C0027051 Myocardial infarction HSDN C4084766 Vomiting C1855109 Methylmalonic aciduria cbla type HPO C3641756 Have diarrhea C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C1557397 Adverse event associated with pain C0017160 Gastroenteritis HSDN C4085211 Pain distress question C0022366 Jaw, edentulous HSDN C0009676 Confusion state C0015632 Encephalitis, far eastern russian MalaCards C0042024 Urine incontinence C3554520 Ufs2 MalaCards C0031911 Pigment deposition C0153536 Malignant melanoma of skin of lower limb MalaCards C3274924 Have been coughing C2937358 Cerebral hemorrhage HSDN C4084725 Usual severity cough C0042830 Perception visual HSDN C4085210 Usual severity pain C0041952 Uerterolithiasis HSDN C1279888 Proteinuria of undiagnosed cause C0008354 Cholera HSDN C4084775 Usual severity weight loss C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C0019572 Hairiness C0086795 Pfaundler-hurler syndrome HPO C0020538 Hbp C0345419 Cutis marmorata telangiectatica congenita MalaCards C1510417 Apraxia of gait C0012746 Dissociative disorder HSDN C0036572 Convulsion C3536564 Atypcial absence seizure, intractable UMLS C0027497 Queasy C2697368 Gastrointestinal irritation UMLS C3887638 Failure to thrive in infant C0041107 Trisomy HSDN C0004134 Dyssynergia C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards C0026858 Musculoskeletal pain C3178777 Bisphosphonate associated osteonecrosis of the jaw HSDN C3898969 Have been vomiting C0162531 Hereditary coproporphyria HSDN|HPO C0150055 Pain chronic C1443291 Complex regional pain syndrome type ii of the upper limb UMLS C4084768 Usual severity vomiting C0025063 Mediastinal neoplasms HSDN C0043094 Weight gain C0023448 Lymphoid leukemia HSDN C4084784 Diarrhea C0023892 Biliary cirrhosis HSDN C0030554 Abnormal sensation C0018946 Hematoma, subdural HSDN C4084775 Usual severity weight loss C2936881 Eosinophilic synovitis MalaCards C0031256 Petechia C0242584 Autoimmune thrombocytopenia MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0024301 Lymphoma, follicular HSDN C0026821 Cramp C0011881 Diabetic nephropathy HSDN C0234146 Absent reflex C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease HPO C0026603 Motion sickness C0029139 Optical illusion HSDN C0237326 Defecation pain C0017689 Glucagonoma OrphaNet|MalaCards C0030193 Sense of pain C1333974 Hepatic extraskeletal osteosarcoma UMLS C3815497 Cough C0010346 Crohn disease HSDN C0231341 Aging premature C0025958 Microcephaly HSDN C0002962 Angina C0036357 Psychology, schizophrenic HSDN C4084767 Bothered by vomiting C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0022107 Fussiness C1420653 Tcn2 gene HPO C0011991 Loose stools C0037274 Dermatologic disorders HSDN C0085636 Light sensitivity C0265201 De sanctis-cacchione syndrome MalaCards|HPO C0042963 Symptoms vomiting C0376550 Astroviridae infection HSDN C0042571 Vertigo subjective C0017160 Gastroenteritis HSDN C0242936 Center pain C0025958 Microcephaly HSDN C0016382 Cutaneous vascular engorgement C0035436 Rheumatic fever MalaCards C4050613 Anxiety C1852467 Creutzfeldt-jakob disease, sporadic MalaCards|HPO C4085548 Usual severity dizziness C1522133 High cholesterol level HSDN C4084723 Constipation C0007131 Non-small cell lung carcinoma HSDN C1135120 Breakthrough pain C0005967 Bone neoplasms HSDN C4084724 Usual severity constipation C0266209 Congenital dilatation of colon MalaCards C0234132 Pyramidal sign C2931441 Hereditary spastic paralysis, infantile onset ascending OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C0206146 Myocardial stunning C0027651 Tumor HSDN C3463815 Feel fatigue C0017638 Glioma HSDN C0037763 Spasm C0010054 Coronary arteriosclerosis HSDN C4084775 Usual severity weight loss C2749861 Mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) MalaCards C1549543 Administration method - pain C0002940 Aneurysm HSDN C2911645 Weight loss adverse event C0013990 Pathological accumulation of air in tissues HSDN C0028738 Nystagmus C1837206 Cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly HPO C0020580 Decreased sensation C0026769 Multiple sclerosis HSDN C0427054 Weakness of neck C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards C4084727 Cough frequency C1963198 Pancreatitis adverse event HSDN C0000737 Abdomen pain C0343376 B; paratyphoid fever DiseaseOntology|MalaCards C0009421 Comatose C0006840 Candidiasis HSDN C4085317 Diarrhea frequency C0856761 Budd-chiari syndrome HSDN C0278152 Hemifacial spasms C0032787 Postoperative complications HSDN C0018926 Emesis bloody C0024228 Lymphatic diseases HSDN C0009676 Confusion state C0011263 Multi-infarct dementia HSDN C4085317 Diarrhea frequency C0439840 Reflex motion descriptor HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1837218 Cleft palate, isolated HSDN C4085210 Usual severity pain C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C0040822 D tremors C0517555 Venous thrombosis after immobility HSDN C0013604 Edematous C1854678 Multiple pterygium syndrome, lethal type MalaCards|HPO C0004604 Pain back C0021799 Interprofessional relations HSDN C0032285 Pneum C1832916 Timothy syndrome MalaCards C4085661 Usual severity nausea C0393626 Opsoclonus-myoclonus syndrome HSDN C0018681 Headache, cephalalgia C0020635 Hypopituitarism HSDN C0015230 Exanthem C1848814 Thymoma, familial MalaCards C1279888 Proteinuria of undiagnosed cause C1857761 Alagille syndrome 2 MalaCards C0003862 Pain joint C2930957 Hantavirosis OrphaNet|MalaCards C1963065 Apnea adverse event C0030567 Parkinson disease HSDN C0349588 Stature short C1859967 Agonadism dextrocardia diaphragmatic hernia MalaCards C0007758 Cerebellar ataxia C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C0018772 Deafness C0340427 Familial dilated cardiomyopathy MalaCards C3146279 Coma C0009373 Colonic diseases HSDN C0349588 Stature short C1857568 Cortical blindness, retardation, and postaxial polydactyly OrphaNet|MalaCards C0030975 Disorders perception C0038661 Suicide HSDN C1963071 Back pain adverse event C0026936 Mycoplasma infections HSDN C1963252 Tremor adverse event C0014121 Bacterial endocarditis HSDN C0036572 Convulsion C0220754 Biotinidase deficiency MalaCards|HPO|UMLS C1963091 Diarrhea adverse event C3489393 Hiatal hernia HSDN C0184567 Pain acute C0016989 Galvanic skin response HSDN C1959630 Eye pain adverse event C0035302 Retinal artery occlusion HSDN C0013404 Respiratory difficulty C1336216 Stage iiia squamous cell carcinoma of lung UMLS C1963184 Nystagmus adverse event C1858479 Spastic paraplegia 11, autosomal recessive OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1735591 Vacterl association MalaCards|HPO C0221170 Stiffness muscle C0342769 Deficiency dehydrogenase lactate MalaCards C0003469 Anxiety disorder C0342443 Adrenal cushing's syndrome MalaCards C0029163 Hemorrhage mouth C0023448 Lymphoid leukemia HSDN C0041834 Erythematous condition C3812646 Drug induced cutaneous vasculitis MalaCards C0042963 Symptoms vomiting C0270611 Brain damage HSDN C0004604 Pain back C3714644 Thymus neoplasms HSDN C0026821 Cramp C0017601 Glaucomas HSDN C2242996 Tingling C0024445 Lipomatosis, familial benign cervical OrphaNet|HPO|MalaCards C3665347 Vision impaired C1854896 Mucolipidosis iii gamma MalaCards C0086439 Activity decreased C0018523 Hallervorden-spatz syndrome HSDN C0037317 Sleep disturbance C0024796 Marfan syndrome OrphaNet|MalaCards C4085211 Pain distress question C0042076 Urologic neoplasms HSDN C0011991 Loose stools C0020615 Hypoglycemia HSDN C2911647 Weight gain adverse event C0009475 Community mental health service HSDN C0518090 Frequency of pain question C0008513 Chorioretinitis HSDN C0042024 Urine incontinence C0751276 Metachromatic leukodystrophy, juvenile type HPO C1279888 Proteinuria of undiagnosed cause C0018946 Hematoma, subdural HSDN C0242936 Center pain C1963084 Colitis adverse event HSDN C0013604 Edematous C0403447 Chronic kidney insufficiency HSDN C0424755 Fever symptoms C0031542 Phlebitis HSDN C0518090 Frequency of pain question C0038273 Stereotypic movement disorder HSDN C0242936 Center pain C0003184 Anthropology HSDN C0231528 Muscle pain generalized C0042470 Guanarito haemorrhagic fever MalaCards C0004134 Dyssynergia C0687751 Acanthocytosis MalaCards C0002962 Angina C0026848 Myopathy HSDN C0004134 Dyssynergia C1850442 Ceroid lipofuscinosis, neuronal, 5 MalaCards|UMLS C4085210 Usual severity pain C0019045 Hemoglobinopathies HSDN C0036572 Convulsion C0393670 Other specified partial epilepsy without mention of impairment of consciousness UMLS C2315100 Pediatric failure to thrive C3809877 Schaaf-yang syndrome MalaCards C0030193 Sense of pain C0043167 Pertussis HSDN C3463815 Feel fatigue C0036220 Kaposi sarcoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0005424 Biliary tract diseases HSDN C0518090 Frequency of pain question C0003492 Aortic coarctation HSDN C0034155 Thrombotic thrombocytopenic purpura C0008309 Bile duct adenoma HSDN C4084775 Usual severity weight loss C2984302 Leishmaniasis infection pathway HSDN C0008031 Pain chest C0037199 Sinusitis HSDN C0036659 Sensation disorder C0037944 Spinal stenosis HSDN C1069915 Vertigo C0520679 Sleep apnea, obstructive HSDN C0007758 Cerebellar ataxia C0028077 Night blindness HSDN C0014591 Bleeding nose C0272350 Dysfibrinogenemia, congenital OrphaNet|HPO|MalaCards C1069915 Vertigo C0038525 Subarachnoid hemorrhage HSDN C0700078 Deep tendon reflex decrease C0265221 Walker-warburg congenital muscular dystrophy MalaCards C0270948 Neurogenic muscular atrophy C0394006 Dysequilibrium syndrome OrphaNet|HPO C0427190 Ataxia, truncal C1832466 Capos syndrome HPO|UMLS C4085862 Bothered by nausea C0036202 Sarcoidosis HSDN C2032396 Pelvic pain on the right C0042063 Urogenital abnormalities HSDN C0221263 Cafe au lait spot C1860707 Tuberous sclerosis 2 (disorder) HPO C2024893 Cardiovascular surgery result: fatigue C0003493 Aortic diseases HSDN C0030193 Sense of pain C0037315 Sleep apnea syndromes HSDN C0026821 Cramp C0007772 Intracranial arteriovenous malformation HSDN C0026826 High muscle tone C0580190 3-phosphoglycerate dehydrogenase deficiency MalaCards C4085317 Diarrhea frequency C0032964 Pregnancy complications, hematologic HSDN C3463815 Feel fatigue C0039590 Testicular neoplasms HSDN C0036572 Convulsion C2931381 Mental retardation x-linked, tranebjaerg type seizures and psoriasis MalaCards C0013362 Dysarthrias C1839564 Jensen syndrome MalaCards C0151786 Weakness muscle C0019054 Hemolysis (disorder) HSDN C0917816 Deficiency mental C1832588 Chromosome 11p11.2 deletion syndrome MalaCards|HPO C0149758 Dentition poor C0024110 Pulmonary abscess UMLS C0009398 Color vision defects C0001723 Affective disorders, psychotic HSDN C0221263 Cafe au lait spot C0027663 Neoplasms, multiple primary HSDN C2237041 Shox gene with short stature C2931146 Radio renal syndrome MalaCards C0018965 Blood urine C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards C3146279 Coma C1956346 Coronary artery disease HSDN C0557874 Global developmental delay C3275487 Cerebral-cerebellar-coloboma syndrome, x-linked MalaCards C4085211 Pain distress question C0035854 Rosacea HSDN C0003467 Angst C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C2984057 Have nausea C0034194 Pyloric stenosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030925 Peptic ulcer with penetration HSDN C0019079 Bloody sputum C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C1963091 Diarrhea adverse event C0035457 Rhinitis, allergic, perennial HSDN C0040259 Tinea pedis C0221391 Melanosis coli HSDN C0000727 Abdomen acute C0024121 Lung neoplasms HSDN C1962972 Proteinuria adverse event C1866075 Glomerulopathy with fibronectin deposits 2 (disorder) OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0030354 Papilloma HSDN C0162298 Stiffness joints C1868678 Thanatophoric dysplasia, type i (disorder) MalaCards|HPO C0024031 Back pain lower back C0018571 Hand injury HSDN C0026603 Motion sickness C0001973 Alcoholic intoxication, chronic HSDN C0030193 Sense of pain C1504306 Anodontia genus HSDN C0008031 Pain chest C1090821 Sepsis (invertebrate) HSDN C0022107 Fussiness C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C0518090 Frequency of pain question C0015670 Child father HSDN C4085211 Pain distress question C0038273 Stereotypic movement disorder HSDN C0013421 Dystonia C0003125 Anorexia nervosa HSDN C0015469 Facial paralysis C0023348 Leprosy, lepromatous HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0497327 Dementia HSDN C4085210 Usual severity pain C0006271 Bronchiolitis HSDN C0038002 Spleen enlargement C3810175 Short-rib thoracic dysplasia 10 with or without polydactyly MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0175754 Agenesis of corpus callosum HSDN C0027796 Neuralgias C0035229 Respiratory insufficiency HSDN C0242936 Center pain C0021141 Inappropriate adh syndrome HSDN C0917816 Deficiency mental C2931092 Maternally inherited leigh syndrome MalaCards C0018681 Headache, cephalalgia C2349476 Chronic migraine without aura nos UMLS C0026838 Spasticity muscle C0024636 Malocclusion HSDN C4084773 Bothered by weight gain C0085426 Gram-positive bacterial infections HSDN C0022346 Yellow skin C1332552 Bile duct mucoepidermoid carcinoma UMLS C1963184 Nystagmus adverse event C0270726 Alexander disease OrphaNet|MalaCards C0020505 Excessive eating C4041080 Neurocognitive disorders HSDN C2242996 Tingling C0007771 Intracranial arteriosclerosis HSDN C0235153 Sensory hallucination C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0019337 Heroin dependence HSDN C1519353 Skin eruption papular C0265964 Mutilating keratoderma MalaCards|HPO C0033774 Skin pruritus C1009209 Tinea HSDN C1549543 Administration method - pain C0162739 Hellp syndrome HSDN C2919142 Short stature adverse event C2931888 Pfeiffer type acrocephalosyndactyly MalaCards C0206146 Myocardial stunning C1963178 Myelitis adverse event HSDN C0033774 Skin pruritus C0001973 Alcoholic intoxication, chronic HSDN C1000483 Genus anemia C1969809 Isobutyryl-coa dehydrogenase deficiency MalaCards|HPO C0033377 Caudal displacement C0034345 Pyruvate dehydrogenase complex deficiency disease MalaCards|HPO C0033790 Pseudobulbar palsy C0243010 Viral encephalitis HSDN C0018681 Headache, cephalalgia C1535939 Pneumocystis jiroveci pneumonia HSDN|UMLS C2911647 Weight gain adverse event C3714644 Thymus neoplasms HSDN C1963093 Dizziness adverse event C0019360 Herpes zoster disease HSDN C0007758 Cerebellar ataxia C1848199 X-linked lissencephaly HPO C3641755 Have constipation C0008628 Chromosome deletion HSDN C0231712 Gait waddling C1846672 Muscular dystrophy, limb-girdle, type 2i MalaCards|HPO|UMLS C4084784 Diarrhea C0149678 Epstein-barr virus infections HSDN C1527344 Dysphonia C0008925 Cleft palate HSDN C4042891 Sleep wake disorders C0036690 Septicemia HSDN C3665346 Loss sight C3279875 Cortical malformations, occipital MalaCards C0030193 Sense of pain C0031048 Pericarditis, constrictive HSDN C0039870 Leanness C0007131 Non-small cell lung carcinoma HSDN C4084769 Vomiting frequency C0018923 Hemangiosarcoma HSDN C0033774 Skin pruritus C1879737 Aromatherapy and essential oils HSDN C0030193 Sense of pain C0037198 Sinus thrombosis, intracranial HSDN C0018932 Bright red rectal bleeding C2674051 Inflammatory bowel disease 11 MalaCards C1549543 Administration method - pain C0162700 Tick-borne diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0021400 Influenza HSDN C4084769 Vomiting frequency C1855109 Methylmalonic aciduria cbla type HPO C0015672 Decreased energy C0031347 Pharyngeal neoplasms HSDN C4084766 Vomiting C1833541 Caroli disease isolated MalaCards C4085210 Usual severity pain C2963140 Arteriovenous fistula in use with two needles HSDN C0085602 Polydypsia C1855849 Bartter syndrome, antenatal , type 2 HPO|UMLS C2362324 Pediatric obesity C1696708 Prehypertension HSDN C4085210 Usual severity pain C0018839 Heat exhaustion HSDN C3898969 Have been vomiting C2713347 7-dehydrocholesterol reductase deficiency MalaCards C0009398 Color vision defects C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0011206 Delirium acute C0020625 Hyponatremia HSDN C0011206 Delirium acute C0029456 Osteoporosis HSDN C0332566 Maculopapule C0343837 Dyschromic skin lesions of carate UMLS C1963071 Back pain adverse event C0025063 Mediastinal neoplasms HSDN C0917816 Deficiency mental C2678039 Mental retardation, x-linked, syndromic 9 MalaCards C3898969 Have been vomiting C0270726 Alexander disease HSDN C4084767 Bothered by vomiting C0027022 Myeloproliferative disease HSDN C0242936 Center pain C4085635 Appetite quality question HSDN C4084775 Usual severity weight loss C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C4084774 Have weight loss C0017563 Gingival diseases HSDN C0042571 Vertigo subjective C3714639 Exit block by ecg finding HSDN C3463815 Feel fatigue C0003431 Antisocial personality disorder HSDN C0011991 Loose stools C0025345 Menstruation disturbances HSDN C4084784 Diarrhea C0010606 Adenoid cystic carcinoma HSDN C0015469 Facial paralysis C0282492 Sneddon syndrome MalaCards|HPO C3898969 Have been vomiting C0024116 Lung diseases, fungal HSDN C1963093 Dizziness adverse event C0040128 Thyroid diseases HSDN C4085210 Usual severity pain C0013418 Abnormal labor HSDN C2984058 Have pain C0235833 Congenital diaphragmatic hernia HSDN C0022346 Yellow skin C0003469 Anxiety disorders HSDN C0019572 Hairiness C0023418 Leukemia HSDN C0015970 Fever unknown origin C0039128 Syphilis HSDN C4085211 Pain distress question C0031149 Peritoneal neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0023448 Lymphoid leukemia HSDN C2024878 Cardiovascular surgery result: dyspnea C0001175 Acquired immunodeficiency syndrome HSDN C0012833 Dizzy C1963229 Retinal detachment adverse event HSDN C0233993 Sexuality related problems C0234024 Relative frigidity UMLS C1557397 Adverse event associated with pain C0006261 Bronchial diseases HSDN C0005779 Clotting C1861451 Stormorken syndrome OrphaNet|HPO|MalaCards C1999266 Depression adverse event C1834846 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 HPO C1963252 Tremor adverse event C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C0034151 Hyperglobulinemic purpura C0039082 Syndrome HSDN C3665347 Vision impaired C1865695 Spondylometaphyseal dysplasia, axial OrphaNet|MalaCards C2034123 Paralysis of right arm C0154703 Upper extremity paralysis UMLS C2237041 Shox gene with short stature C2930852 Zellweger leukodystrophy MalaCards C2024893 Cardiovascular surgery result: fatigue C0003962 Ascites HSDN C0521668 Thunderclap headache C0242342 Sheehan syndrome MalaCards C2237041 Shox gene with short stature C2751318 Nijmegen breakage syndrome-like disorder MalaCards|HPO C2911647 Weight gain adverse event C0282616 Aids enteropathy HSDN C4084766 Vomiting C0079631 Interdisciplinary communication HSDN C0037317 Sleep disturbance C1510479 Neuralgic amyotrophy MalaCards|HPO C0019209 Large liver C1849437 Mainzer-saldino disease MalaCards|HPO C2315100 Pediatric failure to thrive C0268080 Hypercalcemia, idiopathic, of infancy HPO C0917816 Deficiency mental C0796204 Worster-drought syndrome MalaCards C0030200 Intractable pain C0460137 Push down or depress HSDN C2107732 Consistent heat intolerance C0162359 Christ-siemens-touraine syndrome MalaCards|HPO C0751837 Gait ataxic C4225153 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 1 UMLS C0518090 Frequency of pain question C0085399 Ehrlichiosis HSDN C4084784 Diarrhea C0018671 Head and neck neoplasms HSDN C2165512 Depression alternating with periods of elation C0154437 Atypical depressive disorder UMLS C0030193 Sense of pain C0023374 Lesch-nyhan syndrome HSDN C1557397 Adverse event associated with pain C0152156 Dystocia HSDN C0024031 Back pain lower back C0009730 Spinal meningocele HSDN C4084768 Usual severity vomiting C0236969 Substance-related disorders HSDN C0008031 Pain chest C0586323 Alcohol withdrawal seizures UMLS C1962972 Proteinuria adverse event C0011615 Dermatitis, atopic HSDN C3146279 Coma C0025202 Melanoma HSDN C1549543 Administration method - pain C1285666 Drinking behavior HSDN C0013362 Dysarthrias C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C0002962 Angina C0027663 Neoplasms, multiple primary HSDN C0027498 Nausea vomiting C0268314 Cholestasis-edema syndrome, norwegian type OrphaNet|MalaCards C0013421 Dystonia C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C4085317 Diarrhea frequency C0043397 Yellow fever, jungle MalaCards C3815497 Cough C0162359 Christ-siemens-touraine syndrome OrphaNet|MalaCards C0015672 Decreased energy C0007131 Non-small cell lung carcinoma HSDN C0013395 Indigestion C1333761 Gastric adenosquamous carcinoma UMLS C0018681 Headache, cephalalgia C0005396 Bile duct neoplasms HSDN C4084725 Usual severity cough C0013473 Eating disorders HSDN C3665347 Vision impaired C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C0237326 Defecation pain C0268412 Infantile hypophosphatasia MalaCards|HPO C0232462 Appetite decrease C0011989 Camurati-engelmann syndrome MalaCards|HPO C2029884 Hearing loss by exam C0034186 Pyelonephritis HSDN C0086565 Liver function abnormal C0023787 Lipodystrophy MalaCards C4084776 Weight loss C3665624 Serum calcium below normal HSDN C0020672 Body temperature decreased C3244301 Coverage level - family HSDN C3898969 Have been vomiting C0014335 Enteritis HSDN C0039070 Collapse fleeting C0027404 Narcolepsy MalaCards|HPO C0013604 Edematous C0014236 Endophthalmitis HSDN C0349588 Stature short C0432262 Dysosteosclerosis OrphaNet|HPO|MalaCards C0012833 Dizzy C0025149 Medulloblastoma MalaCards C0030554 Abnormal sensation C0022660 Kidney failure, acute HSDN C4084768 Usual severity vomiting C0521607 Peritoneal fibrosis HSDN C0022346 Yellow skin C0026946 Mycoses HSDN C0004604 Pain back C0007766 Intracranial aneurysm HSDN C0242936 Center pain C0020635 Hypopituitarism HSDN C1963087 Constipation adverse event C3280479 Pitt-hopkins-like syndrome 2 MalaCards C0009421 Comatose C1556682 Adverse event associated with infection HSDN C0520966 Coordination impaired C3472711 Spinocerebellar ataxia 36 MalaCards|UMLS C0013456 Pain ear C0027651 Tumor HSDN C0036659 Sensation disorder C0025202 Melanoma HSDN C0424755 Fever symptoms C0017638 Glioma HSDN C0042571 Vertigo subjective C0002895 Anemia, sickle cell HSDN C0011991 Loose stools C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0034150 Skin purpura C1552262 Nurse practitioner - family HSDN C0427068 Legs weakness C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0026640 Mouth neoplasms HSDN C4084727 Cough frequency C3714509 Nutrition disorders HSDN C0015672 Decreased energy C0852007 Scleroderma and associated disorders OrphaNet C0009806 Constipate C2217036 Stage iib colon cancer UMLS C4085210 Usual severity pain C0024904 Mastoiditis HSDN C0018991 Paralysis one side of body C0002949 Aneurysm, dissecting HSDN C4084773 Bothered by weight gain C1691215 Penile hypospadias HSDN C0349506 Sun sensitivity C0024131 Lupus vulgaris MalaCards C1963077 Bone pain adverse event C0342646 Vitamin d-dependent rickets, type 2a HPO C0037763 Spasm C0014549 Tonic-clonic epilepsy HSDN C0007758 Cerebellar ataxia C0025289 Meningitis HSDN C0037383 Sneeze C0032298 Lipid pneumonia HSDN C0023012 Delay language C1970841 Mental retardation, x-linked 93 (disorder) HPO C4084802 Usual severity diarrhea C0034530 Injury radiation HSDN C4085317 Diarrhea frequency C0038436 Post-traumatic stress disorder HSDN C0040822 D tremors C0039006 Swine--diseases HSDN C4085211 Pain distress question C0085437 Meningitis, bacterial HSDN C0009806 Constipate C0279652 Adenocarcinoma of the rectum, colloid UMLS C4084775 Usual severity weight loss C0024121 Lung neoplasms HSDN C3815497 Cough C1963084 Colitis adverse event HSDN C0013421 Dystonia C1963119 Stomach ulcer adverse event HSDN C0033377 Caudal displacement C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C3665347 Vision impaired C2931386 Amaurosis congenita of leber, 3 MalaCards C0004134 Dyssynergia C3554607 Mitochondrial complex iii deficiency, nuclear type 4 MalaCards|UMLS C4085661 Usual severity nausea C1522133 High cholesterol level HSDN C0030486 Extremity paralysis, lower C0041956 Ureteral obstruction HSDN C0020578 Hyperventilate C0018790 Cardiac arrest HSDN C4085661 Usual severity nausea C0023860 Listeriosis DiseaseOntology|MalaCards C0026838 Spasticity muscle C0023676 Life style HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0016397 Focal infection HSDN C4020887 Photodysphoria C0241802 Arthritis, venereal MalaCards C2911647 Weight gain adverse event C0085136 Central nervous system neoplasms HSDN C2984057 Have nausea C0524851 Neurodegenerative disorders HSDN C4084773 Bothered by weight gain C0042384 Vasculitis HSDN C1384666 Decreased hearing C2020284 Stickler syndrome, type 1 MalaCards C4085862 Bothered by nausea C0038828 Arteriomesenteric duodenal ileus HSDN C2984058 Have pain C0007867 Cervix diseases HSDN C0013404 Respiratory difficulty C0280330 Subglottic verrucous carcinoma UMLS C4084788 Have dizziness C0524620 Metabolic syndrome x HSDN C1963065 Apnea adverse event C0206716 Ganglioglioma HSDN C0014591 Bleeding nose C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C0242936 Center pain C0677607 Hashimoto disease HSDN C0518090 Frequency of pain question C3542413 Cdisc adas-cog - comprehension HSDN C0009421 Comatose C0004364 Autoimmune diseases HSDN C0034933 Abnormal reflexes C0038644 Sudden infant death syndrome HSDN C0000737 Abdomen pain C0010633 Cystadenoma HSDN C2024893 Cardiovascular surgery result: fatigue C0042812 Acuity visual HSDN C1963093 Dizziness adverse event C0393911 Pure autonomic failure HSDN C0037763 Spasm C0007137 Squamous cell carcinoma HSDN C0038868 Supranuclear palsy progressive C0751870 Heredodegenerative disorders, nervous system HSDN C1279888 Proteinuria of undiagnosed cause C0027819 Neuroblastoma HSDN C0013911 Emaciate C1000483 Genus anemia HSDN C4084768 Usual severity vomiting C0002395 Alzheimer's disease HSDN C0037383 Sneeze C0338586 Vertebral artery dissection HSDN C0002965 Crescendo angina C0001721 Emotional affect HSDN C0018681 Headache, cephalalgia C0037928 Spinal cord diseases HSDN C1961131 Cough adverse event C0273115 Lung injury HSDN C4084788 Have dizziness C0000735 Abdominal neoplasms HSDN C0020305 Fetal edema C0032969 Pregnancy in diabetics HSDN C2024893 Cardiovascular surgery result: fatigue C0023467 Leukemia, myelocytic, acute HSDN C0026821 Cramp C0151860 Acquired porencephaly HSDN C0750394 Wbc low C0024141 Lupus erythematosus, systemic MalaCards C0454644 Delayed language development C1959582 Pten hamartoma tumor syndrome MalaCards C4084774 Have weight loss C0042251 Vaginal diseases HSDN C0020903 Illusion C0007952 Character HSDN C4084802 Usual severity diarrhea C0032914 Pre-eclampsia HSDN C4042891 Sleep wake disorders C0003864 Arthritis HSDN C2911647 Weight gain adverse event C0006277 Bronchitis HSDN C0042571 Vertigo subjective C3661735 Basilar artery migraine, intractable UMLS C0018991 Paralysis one side of body C0795623 Hepatitis a vaccine, inactivated HSDN C0557874 Global developmental delay C3151303 Obesity, hyperphagia, and developmental delay MalaCards C2585575 Recurrent abdominal pains C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C4085210 Usual severity pain C1720887 Female urogenital diseases HSDN C0518090 Frequency of pain question C0037417 Identification, social HSDN C0026838 Spasticity muscle C1522133 High cholesterol level HSDN C2024893 Cardiovascular surgery result: fatigue C1853733 Hemochromatosis, type 4 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0238417 Scorpion sting HSDN C0241165 Skin thickening C0796280 Acromegaloid facial appearance syndrome OrphaNet|HPO|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004933 Behavior modification technique HSDN C4084723 Constipation C0014859 Esophageal neoplasms HSDN C0013395 Indigestion C0007222 Cardiovascular diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033871 Psychiatric status rating scales HSDN C4084802 Usual severity diarrhea C0029410 Osteoarthritis of hip HSDN C3898969 Have been vomiting C0242966 Systemic inflammatory response syndrome HSDN C1961131 Cough adverse event C0007194 Hypertrophic cardiomyopathy HSDN C0020673 Hypothermia (central) (local) C0037933 Spinal diseases HSDN C0018834 Brash C2675891 Chromosome 1q21.1 duplication syndrome MalaCards C0038002 Spleen enlargement C1847973 Persistent polyclonal b-cell lymphocytosis MalaCards|HPO C0018784 Deafness sensorineural C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0231528 Muscle pain generalized C2973529 Leukocytoclastic vasculitis MalaCards C0036572 Convulsion C3553374 Coenzyme q10 deficiency, primary, 5 MalaCards C1963184 Nystagmus adverse event C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0038525 Subarachnoid hemorrhage HSDN C0241210 Speaking delay C1412747 Bbs2 gene HPO C0239377 Upper extremity pain C1861301 Syringomyelia, isolated UMLS C0848203 Male pelvic pain C1458155 Mammary neoplasms HSDN C2911647 Weight gain adverse event C0003469 Anxiety disorders HSDN C4049644 Depression C0017689 Glucagonoma MalaCards C0040822 D tremors C0020473 Hyperlipidemia HSDN C0026838 Spasticity muscle C1838281 Fryns macrocephaly OrphaNet|MalaCards C0162834 Hyperpigmentation C0162309 Adrenoleukodystrophy MalaCards|HPO C2919142 Short stature adverse event C1959582 Pten hamartoma tumor syndrome MalaCards C0242936 Center pain C0013274 Patent ductus arteriosus HSDN C0036396 Sciatica C0002940 Aneurysm HSDN C0349588 Stature short C0342793 Malonic aciduria MalaCards|HPO C2237041 Shox gene with short stature C0162672 Merrf syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C0023434 Chronic lymphocytic leukemia HSDN C4085862 Bothered by nausea C0002726 Amyloidosis HSDN C0700590 Diaphoresis excessive C0150034 Exchange gas impaired UMLS C4085317 Diarrhea frequency C0027092 Myopia HSDN C0034151 Hyperglobulinemic purpura C0002878 Anemia, hemolytic HSDN C0518090 Frequency of pain question C0872996 Q fever vaccine HSDN C0030193 Sense of pain C1565489 Renal insufficiency HSDN C0917816 Deficiency mental C0010314 Cri-du-chat syndrome MalaCards C2037129 Nasal visual field defect in left eye, sudden onset C0018979 Hemianopsia UMLS C1963184 Nystagmus adverse event C0265235 Marshall syndrome MalaCards|HPO C3829611 Nausea frequency C0033968 Psychotherapeutic technique HSDN C0011991 Loose stools C1963083 Cholecystitis adverse event HSDN C0020615 Hypoglycemia nos C1841972 Glucocorticoid receptor deficiency HPO C0015672 Decreased energy C1522133 High cholesterol level HSDN C1961131 Cough adverse event C0276119 Q-fever pneumonia MalaCards C4084769 Vomiting frequency C0042134 Uterine hemorrhage HSDN C0030552 Paralysis partial C0037932 Curvature of spine HSDN C0041657 Consciousness loss C0024141 Lupus erythematosus, systemic HSDN C4085211 Pain distress question C0043407 Yersinia infections HSDN C2984058 Have pain C0015671 Father HSDN C2237041 Shox gene with short stature C2931247 Chromosome 17, trisomy 17q22 OrphaNet|MalaCards C0424755 Fever symptoms C0854421 Hanta viral infections MalaCards C2984057 Have nausea C0001727 Afferent loop syndrome HSDN C4084788 Have dizziness C0036974 Shock HSDN C1549543 Administration method - pain C0001584 Adolescent psychology HSDN C3887873 Hearing loss C0029342 Orthomyxoviridae infections HSDN C0000737 Abdomen pain C2983424 Stage iv hepatocellular carcinoma UMLS C3539022 Pelvic pain decreasing in severity C0024121 Lung neoplasms HSDN C4085862 Bothered by nausea C0017168 Gastroesophageal reflux disease HSDN C0242936 Center pain C0029454 Osteopetrosis HSDN C0518090 Frequency of pain question C0002063 Alkalosis HSDN C0041834 Erythematous condition C0006845 Candidiasis, chronic mucocutaneous OrphaNet|HPO|MalaCards C0015672 Decreased energy C0233315 Premature birth of newborn HSDN C0034150 Skin purpura C0002890 Leukoerythroblastic anemia HSDN C0233565 Bradykinesia C0020179 Huntington disease MalaCards|HPO|UMLS C2242577 Oromandibular dystonia C3554374 Dystonia 24 MalaCards C0042798 Vision dim C0015405 Fungal eye infections HSDN C0349588 Stature short C1739384 Angel shaped phalangoepiphyseal dysplasia OrphaNet|HPO|MalaCards C0027066 Myoclonic jerking C0039223 Tabes dorsalis HSDN C0002622 Amnesias C0344435 Ventricular fibrillation by ecg finding HSDN C0026821 Cramp C0007222 Cardiovascular diseases HSDN C3541349 Syncope C0242707 Ventricular dysfunction, right HSDN C3463815 Feel fatigue C0035412 Rhabdomyosarcoma HSDN C2984058 Have pain C1956418 Torsion abnormality HSDN C0020672 Body temperature decreased C0010823 Cytomegalovirus infections HSDN C1549543 Administration method - pain C0014536 Epidural tumor HSDN C0023012 Delay language C3495483 Amish brittle hair syndrome MalaCards C0030193 Sense of pain C1963088 Cystitis adverse event HSDN C4085862 Bothered by nausea C0241158 Cicatrix skin HSDN C0018784 Deafness sensorineural C1865270 Bartter syndrome, type 4a HPO C0042928 Paralysis vocal cord C0024115 Lung diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027343 Toenail ingrown HSDN C0742312 Chest pain site thoracic suture line C0741025 Chest problem UMLS C0267373 Bleeding intestine C0027830 Neurofibroma MalaCards C0010200 Cough symptom C0023448 Lymphoid leukemia HSDN C0012833 Dizzy C0155501 Vertigo, peripheral UMLS C1961131 Cough adverse event C0018800 Cardiomegaly HSDN C0026821 Cramp C0024115 Lung diseases HSDN C4084784 Diarrhea C1962983 Cataract adverse event HSDN C1549543 Administration method - pain C0003615 Appendicitis MalaCards C3665347 Vision impaired C1862596 Familial hypobetalipoproteinemia MalaCards C4020887 Photodysphoria C2676042 Skin-hair-eye pigmentation, variation in, 4 HPO C0042963 Symptoms vomiting C0031046 Pericarditis HSDN C0015938 Fetal macrosomia C0413398 Accidental decapitation HSDN C4084766 Vomiting C0162666 Mitochondrial encephalomyopathies HSDN C4085548 Usual severity dizziness C0015806 Femur neck fracture HSDN C0019079 Bloody sputum C0009324 Ulcerative colitis HSDN C0018784 Deafness sensorineural C0162666 Mitochondrial encephalomyopathies HSDN C3815497 Cough C0037120 Pneumonia, nitrogen dioxide HSDN C0234378 Postural tremor C0270736 Essential tremor UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3714644 Thymus neoplasms HSDN C4084723 Constipation C0038395 Streptococcal infections HSDN C2919142 Short stature adverse event C0009207 Cockayne syndrome OrphaNet|MalaCards C3541349 Syncope C0008073 Developmental disabilities HSDN C0042964 Anticipatory vomiting C0009244 Behavioral cognitive therapy HSDN C0015672 Decreased energy C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C0020649 Blood pressure decreased C0279607 Adult primary hepatocellular carcinoma MalaCards C4085211 Pain distress question C1510428 Cerebral abscess HSDN C1836296 Lower extremity weakness C1836295 Spastic paraplegia 28, autosomal recessive (disorder) MalaCards|HPO|UMLS C1549543 Administration method - pain C0001249 Actinobacillus infections HSDN C0035232 Diaphragmatic paralysis C0001118 Acid base imbalance HSDN C0013362 Dysarthrias C1866282 Ceroid lipofuscinosis, neuronal, 6 MalaCards C1963184 Nystagmus adverse event C3150674 Chromosome 15q24 deletion syndrome MalaCards|HPO C4084776 Weight loss C0024437 Macular degeneration HSDN C4084723 Constipation C1963216 Proctitis adverse event HSDN C0398650 Idiopathic thrombocytopenia purpura C0026640 Mouth neoplasms HSDN C0518090 Frequency of pain question C0877792 Sleep disorders, circadian rhythm HSDN C0010038 Corneal opacity disorder C0392475 Roberts-sc phocomelia syndrome MalaCards C3641756 Have diarrhea C0206682 Follicular thyroid carcinoma HSDN C4085642 Level of joint stiffness C3151446 Nestor-guillermo progeria syndrome MalaCards|HPO C1549543 Administration method - pain C0030793 Pelvis tumor HSDN C0030554 Abnormal sensation C0079487 Helicobacter infections HSDN C0034150 Skin purpura C0011606 Exfoliative dermatitis HSDN C0015672 Decreased energy C0002453 Amenorrhea HSDN C0008031 Pain chest C0004096 Asthma HSDN|UMLS C0007859 Pain neck C0011849 Diabetes mellitus HSDN C1963281 Vomiting adverse event C0021053 Immune system diseases HSDN C4084724 Usual severity constipation C1261473 Sarcoma HSDN C0234378 Postural tremor C3539195 Tremor, hereditary essential, 4 MalaCards|UMLS C0016199 Pain flank C3146248 Stage iii renal cell cancer ajcc v7 UMLS C4085548 Usual severity dizziness C0085541 Epilepsy, frontal lobe HSDN C4084775 Usual severity weight loss C0302280 Adrenogenital syndrome HSDN C0241137 Skin pallor C0264743 Rheumatic fever without heart involvement MalaCards C0013390 Cramps menstrual C0005695 Bladder neoplasm HSDN C0023380 Lethargy C0023524 Leukoencephalopathy, progressive multifocal HSDN C1963091 Diarrhea adverse event C0023220 Leg injury HSDN C0036572 Convulsion C0270824 Epilepsy visual UMLS C0019209 Large liver C1864997 Majeed syndrome OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C0004093 Asthenia C0027804 Fatigue neurosis UMLS C0005745 Blepharoptosis C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C1963086 Confusion adverse event C0010054 Coronary arteriosclerosis HSDN C0241137 Skin pallor C2984302 Leishmaniasis infection pathway HSDN C0518090 Frequency of pain question C0149721 Left ventricular hypertrophy HSDN C0015230 Exanthem C2973529 Leukocytoclastic vasculitis MalaCards C0018681 Headache, cephalalgia C1332282 Anaplastic astrocytoma of cerebral hemisphere UMLS C0413252 Hypothermia due to exposure C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards C0039070 Collapse fleeting C1836906 Arrhythmogenic right ventricular dysplasia, familial, 9 HPO|UMLS C0497247 Blood pressure elevation C1866075 Glomerulopathy with fibronectin deposits 2 (disorder) OrphaNet|HPO|MalaCards C0522224 Palsied C0003469 Anxiety disorders HSDN C1963184 Nystagmus adverse event C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037313 Sleep HSDN C1579931 Depressed - symptom C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C1961131 Cough adverse event C0023895 Liver diseases HSDN C0040822 D tremors C0035243 Respiratory tract infections HSDN C0004134 Dyssynergia C0338430 Limbic encephalitis HSDN C0018991 Paralysis one side of body C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0002962 Angina C2004491 Cicatrix HSDN C0020673 Hypothermia (central) (local) C0024141 Lupus erythematosus, systemic HSDN C0018834 Brash C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C2911647 Weight gain adverse event C0344435 Ventricular fibrillation by ecg finding HSDN C0010200 Cough symptom C0023240 Legionellosis OrphaNet|MalaCards C0020578 Hyperventilate C0036202 Sarcoidosis HSDN C4084773 Bothered by weight gain C0026946 Mycoses HSDN C4084724 Usual severity constipation C0034885 Rectal neoplasms HSDN C0242936 Center pain C0023786 Mucopolysaccharidosis i HSDN C0022346 Yellow skin C0022116 Ischemia HSDN C4084769 Vomiting frequency C0013364 Dysautonomia, familial HPO C2984058 Have pain C0016558 Forensic psychiatri HSDN C4084784 Diarrhea C0018482 Haemophilus infections HSDN C0004093 Asthenia C0947912 Myasthenias UMLS C2237041 Shox gene with short stature C1832439 Mievis verellen-dumoulin syndrome OrphaNet|MalaCards C4085641 Level of joint pain C0494042 Spirillosis MalaCards C0013604 Edematous C0040761 Transposition of great vessels HSDN C0018772 Deafness C0013922 Embolism HSDN C0019572 Hairiness C0206686 Adrenocortical carcinoma HSDN C0016199 Pain flank C0022660 Kidney failure, acute HSDN C0426579 Anorexia symptom C0027643 Neoplasm recurrence, local HSDN C0030193 Sense of pain C3714535 Malocclusion, angle class ii HSDN C1963071 Back pain adverse event C1963198 Pancreatitis adverse event HSDN C0012833 Dizzy C0051981 Anti-leprosy vaccine HSDN C0700078 Deep tendon reflex decrease C0039292 Tangier disease MalaCards|HPO C0019572 Hairiness C0003811 Cardiac arrhythmia HSDN C4085548 Usual severity dizziness C0034088 Pulmonary valve insufficiency HSDN C1963091 Diarrhea adverse event C1546635 Specimen source codes - fistula HSDN C4084766 Vomiting C0011849 Diabetes mellitus HSDN C0028738 Nystagmus C3888098 Cataract, autosomal recessive congenital 1 MalaCards C1963252 Tremor adverse event C0019159 Hepatitis a HSDN C0036572 Convulsion C0085281 Addictive behavior HSDN C2984058 Have pain C0014901 Aesthetic HSDN C4042891 Sleep wake disorders C0006434 Burn injury HSDN C0013395 Indigestion C0021364 Male infertility HSDN C0042025 Urinary incontinence stress C0004623 Bacterial infections HSDN C0037199 Sinus infection C0004135 Ataxia telangiectasia MalaCards|HPO C0277799 Fever intermittent C0268390 Muckle-wells syndrome MalaCards|HPO C0003862 Pain joint C0878675 Erdheim-chester disease HSDN C3539022 Pelvic pain decreasing in severity C0022116 Ischemia HSDN C0013362 Dysarthrias C2717757 Retinocochleocerebral vasculopathies MalaCards C0424755 Fever symptoms C0002453 Amenorrhea HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0020506 Hyperpituitarism HSDN C0426649 Bowel spasm C0152167 Anal spasms UMLS C0022346 Yellow skin C0005695 Bladder neoplasm HSDN C4085210 Usual severity pain C0037228 Size perception HSDN C4084767 Bothered by vomiting C1385938 Acanthocephaliasis MalaCards C0476273 Distress respiratory C1710499 Type iii pleuropulmonary blastoma UMLS C4084775 Usual severity weight loss C0009450 Disease caused by microorganism HSDN C0020903 Illusion C0043019 Lateral medullary syndrome HSDN C0917816 Deficiency mental C2673257 Epilepsy, progressive myoclonic 3 HPO C3887638 Failure to thrive in infant C3151147 Bile acid synthesis defect, congenital, 3 MalaCards|HPO C0042024 Urine incontinence C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C2024893 Cardiovascular surgery result: fatigue C1510412 Pseudoaneurysm HSDN C0040822 D tremors C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO|UMLS C0018777 Deafness, conductive C0431406 Asymmetric crying face association OrphaNet|HPO C1963281 Vomiting adverse event C2711591 Infection by anisakidae HSDN C0031315 Phantom limb pain C0025183 Meige syndrome HSDN C0023015 Language handicap C1704771 Association class HSDN C0454644 Delayed language development C2363129 Benign rolandic epilepsy MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0022408 Arthropathy HSDN C1069915 Vertigo C0020676 Hypothyroidism HSDN C2024893 Cardiovascular surgery result: fatigue C1956346 Coronary artery disease HSDN C4084767 Bothered by vomiting C0262584 Carcinoma, small cell HSDN C0030193 Sense of pain C0004114 Astrocytoma HSDN C0007166 Cardiac output decreased C0010356 Cross infection HSDN C0027066 Myoclonic jerking C0031117 Peripheral neuropathy HSDN C0012833 Dizzy C0524812 Intracranial hypotension HSDN C4084784 Diarrhea C0085073 Prosthesis-related infection HSDN C0011991 Loose stools C0085277 Munchausen by proxy syndrome HSDN C0344315 Mood depressed C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C0151908 Dry skin C0220998 Hypothalamic hypothyroidism MalaCards C0000727 Abdomen acute C0030781 Peliosis hepatis HSDN C4084775 Usual severity weight loss C0037369 Smoking HSDN C0151786 Weakness muscle C2985524 Rhabdoid tumor predisposition syndrome MalaCards C2237041 Shox gene with short stature C3280489 Feingold syndrome 2 MalaCards C0027796 Neuralgias C0748226 Radial neuropathy HSDN C4084767 Bothered by vomiting C0031269 Peutz-jeghers syndrome MalaCards|HSDN|HPO C1963091 Diarrhea adverse event C0949272 Iieocolitis MalaCards C0028738 Nystagmus C0033800 Pseudoglioma MalaCards C0027498 Nausea vomiting C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0041105 Jaw spasm C0206645 Desmoplastic fibroma HSDN C0278134 Anesthesias C1527231 Adrenomyeloneuropathy MalaCards C0041105 Jaw spasm C0027149 Myxoma HSDN C0086565 Liver function abnormal C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0000737 Abdomen pain C0267370 Angiodysplasia of colon HSDN C0034933 Abnormal reflexes C0039145 Syringomyelia and syringobulbia HSDN C0575081 Abnormal gait C0007965 Chediak-higashi syndrome MalaCards|HPO C0009421 Comatose C0282687 Hemorrhagic fever, ebola MalaCards C3541349 Syncope C0032285 Pneumonia HSDN C0233514 Behavior abnormal C0032897 Prader-willi syndrome OrphaNet|MalaCards C0035229 Respiratory function impaired C3502298 Lactic acidosis, fatal infantile MalaCards C1963252 Tremor adverse event C0042594 Vestibular diseases HSDN C0040034 Thrombocytopenia C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards|HPO C0030554 Abnormal sensation C0036202 Sarcoidosis HSDN C0424072 Hallucinations, visual, formed C0563611 Formed hallucinations of objects UMLS C0851578 Disorder sleep C2937358 Cerebral hemorrhage HSDN C3898969 Have been vomiting C2240374 Eosinophil count raised HSDN C0242936 Center pain C0008149 Chlamydia infections HSDN C1963281 Vomiting adverse event C0028433 Nose neoplasms HSDN C2984058 Have pain C0040196 Tick infestations HSDN C3539893 Pelvic pain occurs with intercourse C0206654 Leiomyomatosis HSDN C2984058 Have pain C0040761 Transposition of great vessels HSDN C4085210 Usual severity pain C0025637 Methemoglobinemia HSDN C0026838 Spasticity muscle C0268262 Metachromatic leukodystrophy due to saposin b deficiency UMLS C1557397 Adverse event associated with pain C0032131 Plasmacytoma HSDN C2203646 Jaundice C0038661 Suicide HSDN C0151786 Weakness muscle C2827407 Infectious otitis media HSDN C0004134 Dyssynergia C1843366 Niemann-pick disease, type c2 MalaCards|HPO C0041834 Erythematous condition C1851502 Erythema palmare hereditarium MalaCards C0028738 Nystagmus C1263846 Attention deficit hyperactivity disorder MalaCards C3539896 Pelvic pain occurs with urination C0684743 Malignant neoplasm of muscle HSDN C0027066 Myoclonic jerking C0022336 Creutzfeldt-jakob disease MalaCards|HPO|UMLS C4085862 Bothered by nausea C0025281 Meniere disease HSDN C0184567 Pain acute C0022976 Animal gait disorder HSDN C0007166 Cardiac output decreased C0020473 Hyperlipidemia HSDN C0424755 Fever symptoms C3279664 Emberger syndrome MalaCards C4084727 Cough frequency C0268243 Niemann-pick disease, type b HSDN C4085211 Pain distress question C0040553 Toxocariasis HSDN C3887873 Hearing loss C0016510 Foot diseases HSDN C0424755 Fever symptoms C0856761 Budd-chiari syndrome OrphaNet|HPO|MalaCards C0151740 Intracranial hypertension C1622510 Neurocytoma MalaCards C2242996 Tingling C0037299 Skin ulcer HSDN C2024893 Cardiovascular surgery result: fatigue C0025286 Meningioma HSDN C0020305 Fetal edema C0025063 Mediastinal neoplasms HSDN C0031154 Peritonitis, nos C0585274 Periodic syndrome HPO C0018991 Paralysis one side of body C0003850 Arteriosclerosis HSDN C0557874 Global developmental delay C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) HPO C4084767 Bothered by vomiting C0268548 Hyperargininemia MalaCards|HPO C0042420 Vasovagal episode C0085298 Sudden cardiac death HSDN C1963184 Nystagmus adverse event C1856057 Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type OrphaNet|HPO C0035232 Diaphragmatic paralysis C0041296 Tuberculosis HSDN C4084788 Have dizziness C0024141 Lupus erythematosus, systemic HSDN C0151889 Reflexes tendon increased C3554605 Mc3dn2 MalaCards C4084775 Usual severity weight loss C0041755 Adverse reaction to drug HSDN C0040034 Thrombocytopenia C0019100 Severe dengue DiseaseOntology|MalaCards C0010200 Cough symptom C0005586 Bipolar disorder HSDN C2096293 Ent surgical result ear vertigo C0017636 Glioblastoma HSDN C0030193 Sense of pain C3203360 Suppuration HSDN C0015672 Decreased energy C0038663 Suicide attempt HSDN C0575081 Abnormal gait C0013423 Dystonia musculorum deformans OrphaNet|HPO|MalaCards C4084766 Vomiting C0006261 Bronchial diseases HSDN C0041105 Jaw spasm C0936248 Chondroma HSDN C4084766 Vomiting C0019243 Angioedemas, hereditary HPO C0028738 Nystagmus C1865596 Desmosterolosis MalaCards|HPO C0037384 Snore C0011581 Depressive disorder HSDN C1279888 Proteinuria of undiagnosed cause C2984291 Glioblastoma multiforme pathway HSDN C0031911 Pigment deposition C0474824 Halo nevus MalaCards C0042963 Symptoms vomiting C2984291 Glioblastoma multiforme pathway HSDN C0019079 Bloody sputum C1336116 Stage ia large cell carcinoma of lung UMLS C4085210 Usual severity pain C0012817 Diverticulum HSDN C2024893 Cardiovascular surgery result: fatigue C0037397 Behavior social HSDN C0042024 Urine incontinence C0393911 Pure autonomic failure MalaCards C4085210 Usual severity pain C0032780 Postmortem changes HSDN C0575081 Abnormal gait C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant OrphaNet|HPO C4085211 Pain distress question C0031485 Phenylketonurias HSDN C2024893 Cardiovascular surgery result: fatigue C0751674 Lymphangioleiomyomatosis MalaCards|HPO C1962972 Proteinuria adverse event C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C0018772 Deafness C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C3887638 Failure to thrive in infant C1970456 Surfactant metabolism dysfunction, pulmonary, 3 MalaCards|HPO C4084726 Distress cough C2931916 Midline granulomatosis MalaCards C3641755 Have constipation C0001206 Acromegaly HSDN C2237041 Shox gene with short stature C1969562 Mental retardation, autosomal dominant 1 HPO C0023015 Language handicap C0011263 Multi-infarct dementia HSDN C0917816 Deficiency mental C0175692 Johanson-blizzard syndrome OrphaNet|HPO|MalaCards C4084776 Weight loss C0027746 Nerve degeneration HSDN C4084784 Diarrhea C0006075 Bovine virus diarrhea mucosal disease HSDN C0030554 Abnormal sensation C0014474 Ependymoma HSDN C0000727 Abdomen acute C0010356 Cross infection HSDN C0003862 Pain joint C0023343 Leprosy HSDN C0018681 Headache, cephalalgia C1332906 Cerebral glioblastoma UMLS C0039070 Collapse fleeting C0919267 Ovarian neoplasm HSDN C2919142 Short stature adverse event C0268248 Niemann pick disease, adult non neuronopathic MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C3280100 Nephrotic syndrome, type 6 MalaCards C3898969 Have been vomiting C3495422 Finding relating to sexuality and sexual activity HSDN C0151908 Dry skin C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C3494358 Characteristic, prodromal C0011303 Demyelinating diseases HSDN C2911645 Weight loss adverse event C0149521 Pancreatitis, chronic HSDN C0015469 Facial paralysis C0997768 Glaucoma HSDN C1565249 Limitation, mobility C0029408 Degenerative polyarthritis HSDN C2919142 Short stature adverse event C1836121 Al-gazali syndrome MalaCards C0242936 Center pain C0020437 Hypercalcemia HSDN C4084725 Usual severity cough C0008628 Chromosome deletion HSDN C4085317 Diarrhea frequency C0001420 Papillary adenocarcinoma HSDN C0004604 Pain back C0220981 Metabolic acidosis HSDN C4084776 Weight loss C0013595 Eczema HSDN C0026838 Spasticity muscle C0011127 Pressure ulcer HSDN C0017672 Pain tongue C0031212 Personality disorders HSDN C0000727 Abdomen acute C0004669 Bacteroides infections HSDN C2024893 Cardiovascular surgery result: fatigue C0016563 Form perception HSDN C0030193 Sense of pain C0031269 Peutz-jeghers syndrome HSDN C0020578 Hyperventilate C0025062 Mediastinal emphysema HSDN C0751495 Seizure focal C0393734 Complex partial status epilepticus UMLS C0700078 Deep tendon reflex decrease C0238190 Inclusion body myositis (disorder) MalaCards C0004134 Dyssynergia C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0003862 Pain joint C0025202 Melanoma HSDN C0030552 Paralysis partial C0812437 Oculo-dento-digital syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0029001 Onchocerciasis HSDN C0040264 Ear ringing sound C0796561 Melanoma vaccines HSDN C0424755 Fever symptoms C0019101 Hemorrhagic fever with renal syndrome DiseaseOntology|OrphaNet|MalaCards C0022346 Yellow skin C2937358 Cerebral hemorrhage HSDN C0015300 Ocular proptosis C1859406 Borrone di rocco crovato syndrome MalaCards C4085661 Usual severity nausea C0016045 Fibroma HSDN C0042963 Symptoms vomiting C0002991 Cutaneous fibrous histiocytoma HSDN C0454644 Delayed language development C2675486 Chromosome 6pter p24 deletion syndrome OrphaNet|MalaCards C0009792 Consciousness disorder C0030492 Parapsychology HSDN C4084724 Usual severity constipation C0014544 Epilepsy HSDN C0043094 Weight gain C0025521 Inborn errors of metabolism HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3542413 Cdisc adas-cog - comprehension HSDN C0035078 Failure kidney C1839874 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis OrphaNet|HPO C0018681 Headache, cephalalgia C1334928 Necrotic changes (finding) HSDN C3665492 Pigmentations C1333962 Hepatic angiomyolipoma MalaCards C0162275 Ketoaciduria C1832386 Diabetes mellitus, transient neonatal, 1 OrphaNet|HPO|MalaCards C0018991 Paralysis one side of body C0022698 Kinesics HSDN C2132198 Abnormal blistering of the skin C2675683 Epidermolysis bullosa dystrophica with subcorneal cleavage HPO C0518090 Frequency of pain question C0031485 Phenylketonurias HSDN C1963087 Constipation adverse event C0007095 Carcinoid tumor HSDN C0022346 Yellow skin C0302148 Blood clot HSDN C0013404 Respiratory difficulty C1552262 Nurse practitioner - family HSDN C4042891 Sleep wake disorders C0101725 Receptor for advanced glycation endproducts HSDN C0917816 Deficiency mental C0406727 Orofaciodigital syndrome 4 MalaCards C1279888 Proteinuria of undiagnosed cause C0019104 Hemorrhagic fevers, viral HSDN C2911647 Weight gain adverse event C0035229 Respiratory insufficiency HSDN C0004604 Pain back C0520779 Human ehrlichial infection, sennetsu type MalaCards C1963281 Vomiting adverse event C0017668 Focal glomerulosclerosis HSDN C4084767 Bothered by vomiting C0024636 Malocclusion HSDN C0036572 Convulsion C1843014 Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques HPO C0005745 Blepharoptosis C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0020673 Hypothermia (central) (local) C0268353 Cutis laxa, x-linked MalaCards C0042963 Symptoms vomiting C0008924 Cleft lip HSDN C4084784 Diarrhea C0032963 Pregnancy complications, cardiovascular HSDN C4085862 Bothered by nausea C3711850 Opticospinal multiple sclerosis MalaCards C4084725 Usual severity cough C3495422 Finding relating to sexuality and sexual activity HSDN C0424755 Fever symptoms C0085655 Polymyositis OrphaNet|MalaCards C0028738 Nystagmus C1857352 Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy OrphaNet|MalaCards C0013604 Edematous C0018790 Cardiac arrest HSDN C1090821 Sepsis C0400827 Proctitis radiation MalaCards C0002170 Alopecia disorders C0040953 Trichotillomania MalaCards|HPO C0030552 Paralysis partial C3854315 Pseudoprimary hyperaldosteronism MalaCards|HSDN C0577655 Quadricep weakness C0270968 Limb-girdle muscular dystrophy type 2h MalaCards|HPO|UMLS C0018524 Hallucinate C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C0034933 Abnormal reflexes C1168250 Laryngopharyngeal reflux HSDN C4084725 Usual severity cough C0032963 Pregnancy complications, cardiovascular HSDN C0036659 Sensation disorder C0796147 Acrocallosal syndrome HSDN C0150055 Pain chronic C0024408 Machado-joseph disease MalaCards|HPO|UMLS C0033774 Skin pruritus C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0042798 Vision dim C2751309 Achromatopsia 5 MalaCards|HPO C1384666 Decreased hearing C2931842 Diaphyseal dysplasia 1, progressive MalaCards|HPO C0030193 Sense of pain C0079731 B-cell lymphomas HSDN C4084776 Weight loss C0034067 Pulmonary emphysema HSDN C1962972 Proteinuria adverse event C0004352 Autistic disorder HSDN C0700292 Arterial hypoxaemia C0878555 Diffuse panbronchiolitis MalaCards C0349489 Fetal hypoxia C0032964 Pregnancy complications, hematologic HSDN C4085317 Diarrhea frequency C0155862 Streptococcal pneumonia HSDN C3641755 Have constipation C0023470 Myeloid leukemia HSDN C0700078 Deep tendon reflex decrease C0268631 Succinic semialdehyde dehydrogenase deficiency MalaCards|HPO C4085661 Usual severity nausea C0005750 Blind loop syndrome HSDN C0040485 Wryneck C0079173 Craniomandibular disorders HSDN C4085317 Diarrhea frequency C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C3541349 Syncope C0007570 Celiac disease HSDN C0030193 Sense of pain C0848558 Hypospadias HSDN C2242996 Tingling C0040021 Thromboangiitis obliterans OrphaNet|MalaCards C0010520 Skin cyanosis C0008350 Cholelithiasis HSDN C0231528 Muscle pain generalized C0039516 Tennis elbow HSDN C4085549 Dizziness C0007137 Squamous cell carcinoma HSDN C4084784 Diarrhea C0007121 Bronchogenic carcinoma HSDN C0022408 Disorder joint C0271568 Laron syndrome HPO C0241137 Skin pallor C0001546 Adjustment disorders HSDN C0026826 High muscle tone C0026850 Muscular dystrophy HSDN C0018681 Headache, cephalalgia C0027947 Neutropenia HSDN C1279888 Proteinuria of undiagnosed cause C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C4084784 Diarrhea C0344435 Ventricular fibrillation by ecg finding HSDN C0018681 Headache, cephalalgia C0006840 Candidiasis HSDN C0086437 Joint hypermobility C3280798 Cutis laxa, autosomal recessive, type ib MalaCards C0009806 Constipate C1963215 Pneumothorax adverse event HSDN C0009024 Clonus C1865409 Amyotrophic lateral sclerosis 4, juvenile MalaCards|HPO C2203646 Jaundice C0004576 Babesiosis OrphaNet|HSDN|MalaCards C0018524 Hallucinate C0042487 Venous thrombosis HSDN C0008031 Pain chest C0032969 Pregnancy in diabetics HSDN C0030193 Sense of pain C0036412 Sclera HSDN C0013404 Respiratory difficulty C1322286 Thymoma, type c OrphaNet|MalaCards C3274924 Have been coughing C0266284 Lingual thyroid HSDN C3887873 Hearing loss C0033968 Psychotherapeutic technique HSDN C0015468 Face pain C1962986 Glaucoma adverse event HSDN C3665347 Vision impaired C1840452 Hyaloideoretinal degeneration of wagner HPO C1963135 Hepatic necrosis adverse event C0220620 Gastrointestinal carcinoid tumor MalaCards C0151825 Ostalgia C0346068 Cobb syndrome OrphaNet|MalaCards C2108109 Continuous electrocardiogram sinus tachycardia C0031511 Pheochromocytoma MalaCards C0009676 Confusion state C0039483 Giant cell arteritis HSDN C0152169 Colic renal C0041328 Renal tuberculosis HSDN C0151827 Pain eye C0398625 Protein c deficiency HSDN C0235153 Sensory hallucination C1837893 Schizophrenia 12 MalaCards C0002170 Alopecia disorders C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C0017181 Gastrointestinal bleed C1851124 Desmoid disease, hereditary MalaCards C0002170 Alopecia disorders C3494506 Pseudohypoparathyroidism, type ia MalaCards C0232466 Feeding difficulty C0268608 Deficiency of dihydrofolate reductase MalaCards C3146279 Coma C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C0018775 Hearing loss bilateral C1999266 Depression adverse event HSDN C0043094 Weight gain C0042769 Virus diseases HSDN C3539896 Pelvic pain occurs with urination C0037929 Spinal cord injuries HSDN C0002170 Alopecia disorders C0268338 Ehlers-danlos syndrome, type iv HPO C0030975 Disorders perception C0029408 Degenerative polyarthritis HSDN C2911645 Weight loss adverse event C0026850 Muscular dystrophy HSDN C0015469 Facial paralysis C0027627 Neoplasm metastasis HSDN C3829611 Nausea frequency C1000587 Pemphigus HSDN C1557397 Adverse event associated with pain C0013369 Dysentery HSDN C0013404 Respiratory difficulty C0034628 Radius fracture HSDN C3539893 Pelvic pain occurs with intercourse C0242350 Erectile dysfunction HSDN C0010038 Corneal opacity disorder C0017083 Gangliosidoses MalaCards C0002624 Amnesia retrograde C0004377 Automatism HSDN C3815497 Cough C0003467 Anxiety HSDN C4085661 Usual severity nausea C0009319 Colitis HSDN C2315100 Pediatric failure to thrive C4012395 Congenital disorder of glycosylation, type iy MalaCards C0036572 Convulsion C0023448 Lymphoid leukemia HSDN C3541349 Syncope C0752138 Intracranial arterial diseases HSDN C0009024 Clonus C4014354 Pontocerebellar hypoplasia, type 9 MalaCards|UMLS C2911647 Weight gain adverse event C1636667 Disorder characterized by eosinophilia HSDN C0344435 Ventricular fibrillation by ecg finding C0035410 Rhabdomyolysis MalaCards C1549543 Administration method - pain C0007135 Adenocarcinoma, scirrhous HSDN C0035229 Respiratory function impaired C0265915 Congenital stenosis, pulmonary veins OrphaNet|MalaCards C0013404 Respiratory difficulty C0001418 Adenocarcinoma HSDN C0476206 Dizziness and giddiness symptoms C0809999 Conditions associated with dizziness or vertigo UMLS C0042798 Vision dim C3150691 Retinitis pigmentosa 54 MalaCards|HPO C4085210 Usual severity pain C0001726 Affective symptoms HSDN C0027066 Myoclonic jerking C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO|UMLS C0000737 Abdomen pain C0278712 Wilm's tumor, stage ii UMLS C0009806 Constipate C1443900 Inhalational botulism OrphaNet|MalaCards C0033774 Skin pruritus C0033839 Pseudorabies HSDN C0030193 Sense of pain C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C1279888 Proteinuria of undiagnosed cause C0001824 Agranulocytosis HSDN C0413252 Hypothermia due to exposure C0853986 Lymphocytes decreased HSDN C0040485 Wryneck C0005940 Bone diseases HSDN C0155047 Visual loss, both eyes unqual. C0809996 Blindness and vision defects UMLS C2032396 Pelvic pain on the right C1458155 Mammary neoplasms HSDN C0004134 Dyssynergia C1859568 Bardet-biedl syndrome 10 HPO C0454644 Delayed language development C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C0237326 Defecation pain C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C4084723 Constipation C2717876 Aciduria, propionic OrphaNet|HPO C0497406 Over weight C0597109 Nurse's role HSDN C1963154 Renal failure adverse event C3280216 Hnfj3 MalaCards C2919142 Short stature adverse event C1832950 Cardiac malformation, cleft lip-palate, microcephaly and digital anomalies HPO C0684343 Pseudophakia C0018425 Gyrate atrophy HSDN C4084784 Diarrhea C0020437 Hypercalcemia HSDN C0017565 Gingiva hemorrhage C0042470 Guanarito haemorrhagic fever MalaCards C0019209 Large liver C2316212 Cryopyrin-associated periodic syndromes MalaCards C0236065 Edema mouth C0151610 Edema tongue UMLS C0007758 Cerebellar ataxia C0034341 Pyruvate carboxylase deficiency disease HSDN C1963071 Back pain adverse event C0008073 Developmental disabilities HSDN C0030193 Sense of pain C0376670 Pancreatitis, alcoholic HSDN C3641756 Have diarrhea C0011616 Contact dermatitis HSDN C0557874 Global developmental delay C0221033 Trisomy x syndrome OrphaNet|MalaCards C0009676 Confusion state C0042594 Vestibular diseases HSDN C0557874 Global developmental delay C3809173 Epileptic encephalopathy, early infantile, 16 MalaCards C0030552 Paralysis partial C0014070 Encephalomyelitis HSDN C4084774 Have weight loss C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C2024893 Cardiovascular surgery result: fatigue C0271270 Oculovestibuloauditory syndrome DiseaseOntology|MalaCards C0015938 Fetal macrosomia C0017547 Gigantism HSDN C0575081 Abnormal gait C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C0013404 Respiratory difficulty C0343525 Lemierre syndrome HSDN C0575081 Abnormal gait C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C0020672 Body temperature decreased C1623041 Breast-fed HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0158454 Malunited fracture HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042266 Vaginismus HSDN C0007814 Cerebrospinal fluid otorrhea C0021890 Intraoperative complications HSDN C1262279 Transient radicular irritation due to spinal anaesthesia C0392008 Anaesthesia complication UMLS C4085641 Level of joint pain C0019163 Hepatitis b DiseaseOntology|MalaCards C0013428 Painful urination C0014457 Eosinophilia HSDN C4084784 Diarrhea C0007570 Celiac disease DiseaseOntology C1963091 Diarrhea adverse event C0003467 Anxiety HSDN C4085862 Bothered by nausea C1522133 High cholesterol level HSDN C0015469 Facial paralysis C0030297 Pancreatic neoplasm HSDN C2984058 Have pain C0878675 Erdheim-chester disease HSDN C0917816 Deficiency mental C0520681 Central alveolar hypoventilation syndrome MalaCards C4085317 Diarrhea frequency C0010034 Corneal diseases HSDN C0427190 Ataxia, truncal C2675211 Episodic ataxia, type 6 (disorder) MalaCards|HPO C3641755 Have constipation C0024228 Lymphatic diseases HSDN C0013362 Dysarthrias C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0011168 Disorder deglutition C1857093 Dystonia 2, torsion, autosomal recessive (disorder) MalaCards|HPO C4085317 Diarrhea frequency C0002949 Aneurysm, dissecting HSDN C0042571 Vertigo subjective C0014457 Eosinophilia HSDN C4084767 Bothered by vomiting C0013010 Cerebral lateralization HSDN C0026884 Muteness C0008076 Child guidance HSDN C4085210 Usual severity pain C0029295 Oropharyngeal neoplasms HSDN C0007166 Cardiac output decreased C4084909 Depression subordinate domain HSDN C4085210 Usual severity pain C0020476 Hyperlipoproteinemias HSDN C0020649 Blood pressure decreased C0010308 Congenital hypothyroidism MalaCards C1963065 Apnea adverse event C0041755 Adverse reaction to drug HSDN C0043094 Weight gain C0004442 Avoidance learning HSDN C4084784 Diarrhea C0022876 Premature obstetric labor HSDN C4085211 Pain distress question C0027438 Nasopharynx HSDN C0426579 Anorexia symptom C1548578 Location characteristic id - smoking HSDN C2911645 Weight loss adverse event C0042140 Uterine prolapse HSDN C0151786 Weakness muscle C0034152 Henoch-schoenlein purpura MalaCards C3887638 Failure to thrive in infant C1857550 11-beta-hydroxysteroid dehydrogenase, type ii HPO C0011991 Loose stools C3281289 Trichohepatoenteric syndrome 2 MalaCards C0042963 Symptoms vomiting C1552527 Clinic / center - developmental disabilities HSDN C1549543 Administration method - pain C0025297 Viral meningitis HSDN C0019209 Large liver C1844412 Liver glycogenosis, x-linked, type ii HPO C0042963 Symptoms vomiting C0010674 Cystic fibrosis HSDN C0009676 Confusion state C0026654 Moyamoya disease HSDN C2187990 Unable to perform sex C0017075 Ganglioneuroma MalaCards C0018772 Deafness C1963088 Cystitis adverse event HSDN C4085222 Nausea C0020542 Pulmonary hypertension HSDN C1963170 Hypothermia adverse event C0027932 Neurotic disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040896 Trichinellosis HSDN C0036572 Convulsion C0042029 Urinary tract infection HSDN C3641756 Have diarrhea C0007873 Uterine cervical neoplasm HSDN C3539895 Pelvic pain occurs with bowel movement C1956346 Coronary artery disease HSDN C1963087 Constipation adverse event C0206042 Fatal familial insomnia HPO C0033774 Skin pruritus C0020458 Hyperhidrosis disorder HSDN C0518090 Frequency of pain question C0026618 Dental fluorosis, acquired HSDN C4085549 Dizziness C3539923 Cdisc adas-cog - orientation summary score HSDN C2984058 Have pain C1963274 Vasculitis adverse event HSDN C3665347 Vision impaired C3151202 Leber congenital amaurosis 8 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0085271 Self-injurious behavior HSDN C0013362 Dysarthrias C2673257 Epilepsy, progressive myoclonic 3 HPO C1971624 Appetite absent C0751202 Cystathionine beta-synthase deficiency disease HPO C0017672 Pain tongue C4049644 Depression HSDN C0035078 Failure kidney C2678045 Toe syndactyly, telecanthus, and anogenital and renal malformations OrphaNet|HPO C4084725 Usual severity cough C0030305 Pancreatitis HSDN C0518090 Frequency of pain question C0017605 Angle closure glaucoma HSDN C0030193 Sense of pain C0017547 Gigantism HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041313 Hepatic tuberculosis HSDN C0018681 Headache, cephalalgia C0030499 Parasitic diseases HSDN C0004093 Asthenia C0014544 Epilepsy HSDN C4084766 Vomiting C0043019 Lateral medullary syndrome HSDN C1963184 Nystagmus adverse event C1860433 Nystagmus 4, congenital, autosomal dominant (disorder) MalaCards C0003469 Anxiety disorder C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0030552 Paralysis partial C0017927 Glycogen storage disease type viii HSDN C1963252 Tremor adverse event C4015420 Epilepsy, progressive myoclonic 7 MalaCards C0015970 Fever unknown origin C0023364 Leptospirosis HSDN C4084776 Weight loss C0019829 Hodgkin disease OrphaNet|HSDN C0018681 Headache, cephalalgia C1332288 Anaplastic secondary supratentorial astrocytoma UMLS C0042928 Paralysis vocal cord C0152025 Polyneuropathy HSDN C4084769 Vomiting frequency C0038536 Subcutaneous emphysema HSDN C0007166 Cardiac output decreased C0019829 Hodgkin disease HSDN C1963087 Constipation adverse event C0036864 Sexual relations HSDN C0015469 Facial paralysis C0017160 Gastroenteritis HSDN C0518090 Frequency of pain question C1253937 Pericardial effusion HSDN C0494475 Seizure generalized tonic clonic C0008626 Congenital chromosomal disease MalaCards C0015672 Decreased energy C1552052 Religious affiliation - meditation HSDN C0234523 Apraxia, classic C0236642 Pick disease of the brain HSDN C0018775 Hearing loss bilateral C0152026 Retinal vasculitis HSDN C0700078 Deep tendon reflex decrease C0152109 Juvenile spinal muscular atrophy HPO C2169806 Tic C0236792 Asperger syndrome HSDN C0349588 Stature short C1859487 Biemond syndrome ii MalaCards C1961131 Cough adverse event C0162429 Malnutrition HSDN C0023380 Lethargy C0011303 Demyelinating diseases HSDN C1549543 Administration method - pain C0007350 Cat disease HSDN C3274924 Have been coughing C0003469 Anxiety disorders HSDN C1963063 Anorexia adverse event C1956390 Cranial arteritis MalaCards C0242936 Center pain C0391889 Bony union HSDN C4084773 Bothered by weight gain C0035235 Respiratory syncytial virus infections HSDN C0234979 Dysdiadochokinesia C3149907 Als13 HPO C0002965 Crescendo angina C2586211 Thrombosis of blood vessel HSDN C4084727 Cough frequency C0000768 Congenital abnormality HSDN C0042928 Paralysis vocal cord C1963064 Anxiety adverse event HSDN C0344315 Mood depressed C0795959 Gomez lopez hernandez syndrome MalaCards C2203646 Jaundice C0032851 Disease poultry HSDN C3714552 Strength decreased C0744971 Hiv lymphadenopathy UMLS C0015468 Face pain C0009240 Cognition HSDN C1963071 Back pain adverse event C0019699 Hiv seropositivity HSDN C1963091 Diarrhea adverse event C0039730 Thalassemia HSDN C0518090 Frequency of pain question C0162700 Tick-borne diseases HSDN C1963281 Vomiting adverse event C1962986 Glaucoma adverse event HSDN C3463815 Feel fatigue C1290398 Cerebral arterial aneurysm HSDN C0036572 Convulsion C3278147 Geleophysic dysplasia 1 MalaCards|UMLS C0349588 Stature short C3151446 Nestor-guillermo progeria syndrome MalaCards|HPO C0233514 Behavior abnormal C0238052 Xanthomatosis, cerebrotendinous OrphaNet|MalaCards C0518090 Frequency of pain question C0019569 Hirschsprung disease HSDN C2096293 Ent surgical result ear vertigo C0474820 Glomerocytoma tympanicum HSDN C3641756 Have diarrhea C0036421 Systemic scleroderma HSDN C0000727 Abdomen acute C0019310 Hernia, obturator HSDN C4085211 Pain distress question C0037268 Skin abnormalities HSDN C0006370 Bulimia C0031873 Pica disease HSDN C0018524 Hallucinate C2931859 Acquired cjd MalaCards C0030193 Sense of pain C1711312 Breast carcinoma with osseous metaplasia UMLS C1971624 Appetite absent C0034494 Rabies (disorder) OrphaNet|MalaCards C0004134 Dyssynergia C0020651 Hypotension, orthostatic HSDN C1962972 Proteinuria adverse event C0033054 Prenatal exposure delayed effects HSDN C1963180 Neck pain adverse event C0014860 Perforation esophagus HSDN C4085210 Usual severity pain C1963164 Lymphopenia adverse event HSDN C0040034 Thrombocytopenia C2677608 Thrombocytopenia 4 MalaCards|HPO C1963137 Hydrocephalus adverse event C1968804 Plasminogen deficiency, type i MalaCards|HPO C2984057 Have nausea C3714644 Thymus neoplasms HSDN C0700078 Deep tendon reflex decrease C0685838 Gonadal dysgenesis xx type deafness MalaCards|HPO C0026821 Cramp C0517555 Venous thrombosis after immobility HSDN C0018681 Headache, cephalalgia C3887654 Polyarteritis nodosa, childhood-onset MalaCards|UMLS C4084775 Usual severity weight loss C0006109 Brain damage, chronic HSDN C0162834 Hyperpigmentation C0021368 Inflammation MalaCards C0036572 Convulsion C0796012 Krause-kivlin syndrome HPO|UMLS C0013362 Dysarthrias C1836474 Spinocerebellar ataxia, autosomal recessive 7 MalaCards C0018772 Deafness C0036472 Scrub typhus HSDN C3665492 Pigmentations C1306468 Ovarian malignant neoplasm primary MalaCards C0004134 Dyssynergia C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0231528 Muscle pain generalized C0043195 Subsepsis hyperergia syndrome OrphaNet|MalaCards C0013404 Respiratory difficulty C0345960 Giant cell carcinoma of lung UMLS C0042963 Symptoms vomiting C0029132 Disorder of the optic nerve HSDN C0019521 Hiccoughs C0024248 Cyst lymph HSDN C0518090 Frequency of pain question C1705810 Generic role HSDN C0020305 Fetal edema C0398368 Lymphatic abnormalities HSDN C0004134 Dyssynergia C0574084 3-methylglutaconic aciduria type 3 OrphaNet|UMLS|HPO|MalaCards C0019209 Large liver C1857276 Trichohepatoenteric syndrome MalaCards|HPO C4084775 Usual severity weight loss C0027726 Nephrotic syndrome HSDN C0020538 Hbp C0268338 Ehlers-danlos syndrome, type iv OrphaNet C0085636 Light sensitivity C0038868 Progressive supranuclear palsy HPO|UMLS C0851578 Disorder sleep C0079631 Interdisciplinary communication HSDN C4084725 Usual severity cough C0001486 Adenovirus infections HSDN C0020458 Hyperhydrosis C0406357 Skin peeling disorder OrphaNet C0032285 Pneum C1865371 Severe combined immunodeficiency, athabaskan-type HPO C0015468 Face pain C0007820 Cerebrovascular disorders HSDN C1963249 Tinnitus adverse event C0010823 Cytomegalovirus infections HSDN C0266996 Sialectasis C0012359 Pathological dilatation UMLS C0042025 Urinary incontinence stress C2020541 Strabismus HSDN C4084724 Usual severity constipation C0042487 Venous thrombosis HSDN C0700078 Deep tendon reflex decrease C3280168 Hsn2c MalaCards C1963086 Confusion adverse event C0041318 Tuberculosis, meningeal HSDN C0022346 Yellow skin C1709568 Pleomorphic hepatocellular carcinoma UMLS C0018772 Deafness C1864825 Frias syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0376549 Roseolovirus infections HSDN C4084769 Vomiting frequency C0028738 Nystagmus HSDN C1963170 Hypothermia adverse event C0014859 Esophageal neoplasms HSDN C0011991 Loose stools C0745138 Hypertensive urgency UMLS C0013604 Edematous C0005818 Blood platelet disorders HSDN C0009421 Comatose C0033923 Psychomotor function HSDN C4084724 Usual severity constipation C0243026 Sepsis HSDN C4085211 Pain distress question C0005747 Blepharospasm HSDN C0728710 Pupil constriction observed C0271051 Macular retinal edema HSDN C0020615 Hypoglycemia nos C3553607 Mitochondrial pyruvate carrier deficiency MalaCards C3539892 Pelvic pain in front C0029456 Osteoporosis HSDN C0015970 Fever unknown origin C0027765 Nervous system disorder HSDN C0242936 Center pain C0238198 Gastrointestinal stromal tumors HSDN C0030552 Paralysis partial C0020428 Hyperaldosteronism MalaCards C4084768 Usual severity vomiting C0268242 Niemann-pick disease, type a MalaCards|HPO C0151740 Intracranial hypertension C1334410 Localized primitive neuroectodermal tumor MalaCards C0042963 Symptoms vomiting C0038159 Food poisoning, staphylococcal DiseaseOntology|MalaCards C0020305 Fetal edema C0022739 Klippel-trenaunay-weber syndrome MalaCards C0858588 Sensory abnormality of lower extremities C0152027 Sensory disorders UMLS C0033774 Skin pruritus C0030807 Pemphigus, nos HSDN C0035078 Failure kidney C0263979 Myositis, purulent MalaCards C0006370 Bulimia C0149573 Structure of posterior inferior cerebellar artery HSDN C0030193 Sense of pain C1963119 Stomach ulcer adverse event HSDN C0349588 Stature short C2931484 Cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation OrphaNet|MalaCards C2911647 Weight gain adverse event C0040425 Tonsillitis HSDN C3203358 Alveolar hypoventilation C1867858 Prader-willi syndrome chromosome region HPO C0349588 Stature short C0282525 Adrenoleukodystrophy, neonatal OrphaNet|HPO|MalaCards C0009676 Confusion state C0032019 Pituitary neoplasms HSDN C1971624 Appetite absent C0009324 Ulcerative colitis HSDN C0917816 Deficiency mental C1846168 Mental retardation, x-linked, syndromic 10 MalaCards|HPO C3539892 Pelvic pain in front C0520946 Emotional hypersensitivity HSDN C1384666 Decreased hearing C0024117 Chronic obstructive airway disease HSDN C0000737 Abdomen pain C1532560 Plasmacytoma - category HSDN C2911645 Weight loss adverse event C0038454 Cerebrovascular accident HSDN C4085862 Bothered by nausea C0023895 Liver diseases HSDN C4084769 Vomiting frequency C0034929 Reflex HSDN C0033774 Skin pruritus C0010068 Coronary heart disease HSDN C0007758 Cerebellar ataxia C0004096 Asthma HSDN C4085211 Pain distress question C0015403 Eye infections HSDN C0018808 Murmur C0007093 Carcinoid heart disease HSDN C4084802 Usual severity diarrhea C0004576 Babesiosis HSDN C0232461 Increased appetite C1720863 Congenital generalized lipodystrophy type 2 MalaCards|HPO C0006370 Bulimia C0036596 Self disclosure HSDN C0035229 Respiratory function impaired C3553449 Pontocerebellar hypoplasia, type 1b MalaCards C1971624 Appetite absent C0032787 Postoperative complications HSDN C3539023 Pelvic pain increasing in frequency C0520676 Premenstrual dysphoric disorder HSDN C2984058 Have pain C0887833 Carcinoma, pancreatic ductal HSDN C0000727 Abdomen acute C0010633 Cystadenoma HSDN C4084775 Usual severity weight loss C0027663 Neoplasms, multiple primary HSDN C1549543 Administration method - pain C0010417 Cryptorchidism HSDN C0000737 Abdomen pain C0278716 Recurrent wilms' tumor and other childhood kidney tumors UMLS C2242996 Tingling C0041601 Ulna fracture HSDN C0848203 Male pelvic pain C0010709 Cyst HSDN C0020578 Hyperventilate C0023467 Leukemia, myelocytic, acute HSDN C0000737 Abdomen pain C0043397 Yellow fever, jungle MalaCards C0013528 Echo speech C0011265 Presenile dementia HSDN C0019572 Hairiness C0003864 Arthritis HSDN C0026838 Spasticity muscle C0009240 Cognition HSDN C1549543 Administration method - pain C0424318 Bullied HSDN C4085862 Bothered by nausea C0001314 Acute disease HSDN C0002622 Amnesias C0038531 Subclavian artery stenosis HSDN C0518090 Frequency of pain question C1720830 Painful bladder syndrome OrphaNet|MalaCards C4084769 Vomiting frequency C0025521 Inborn errors of metabolism HSDN C4020887 Photodysphoria C2931074 Cone rod dystrophy amelogenesis imperfecta OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0003469 Anxiety disorders HSDN C0043094 Weight gain C0001314 Acute disease HSDN C0349588 Stature short C0796003 Juberg-marsidi syndrome HPO C0018772 Deafness C0517960 Neurological status: consciousness HSDN C2029884 Hearing loss by exam C1548578 Location characteristic id - smoking HSDN C0000737 Abdomen pain C0004935 Animal ethology HSDN C2024893 Cardiovascular surgery result: fatigue C0034885 Rectal neoplasms HSDN C0013604 Edematous C0032460 Polycystic ovary syndrome HSDN C0151740 Intracranial hypertension C1864436 Muenke syndrome OrphaNet|HPO|MalaCards C3539889 Pelvic pain increasing in severity C0085096 Peripheral vascular diseases HSDN C1565249 Limitation, mobility C0011581 Depressive disorder HSDN C4084768 Usual severity vomiting C0038661 Suicide HSDN C4085222 Nausea C3889576 Euphoria HSDN C0010038 Corneal opacity disorder C2751316 Glaucoma 3, primary congenital, d MalaCards|HPO C4084784 Diarrhea C0085092 Parenting behavior HSDN C0042571 Vertigo subjective C0398691 Hyperimmunoglobulinemia d MalaCards|HPO C1145670 Failure respiratory C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C0042571 Vertigo subjective C0034067 Pulmonary emphysema HSDN C4084802 Usual severity diarrhea C0024591 Malignant hyperpyrexia due to anesthesia HSDN C1963071 Back pain adverse event C0007117 Basal cell carcinoma HSDN C0151686 Growth retardation C0796028 Ataxia, fatal x-linked, with deafness and loss of vision MalaCards|HPO C4085862 Bothered by nausea C0004030 Aspergillosis HSDN C0012833 Dizzy C0546884 Hypovolemia HSDN C4084775 Usual severity weight loss C0037933 Spinal diseases HSDN C1279888 Proteinuria of undiagnosed cause C0007177 Cardiac tamponade HSDN C4084788 Have dizziness C0024236 Lymphedema HSDN C0085636 Light sensitivity C1510428 Cerebral abscess HSDN C3539893 Pelvic pain occurs with intercourse C0015732 Fecal incontinence HSDN C0018784 Deafness sensorineural C0406704 Rudiger syndrome 1 HPO C1279888 Proteinuria of undiagnosed cause C2025995 Cellulitis HSDN C0557874 Global developmental delay C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C3541349 Syncope C3808145 Left ventricular noncompaction 9 MalaCards C0018772 Deafness C0021603 Sleep initiation and maintenance disorders HSDN C0424755 Fever symptoms C0023473 Myeloid leukemia, chronic OrphaNet|HSDN|HPO C3898969 Have been vomiting C0032266 Emphysema, intestinal HSDN C2919142 Short stature adverse event C2931570 Duplication 4p syndrome OrphaNet|MalaCards C0000737 Abdomen pain C0005396 Bile duct neoplasms HSDN C0009806 Constipate C0342579 Electrolyte imbalance UMLS C0242936 Center pain C0010308 Congenital hypothyroidism HSDN C0015469 Facial paralysis C3148763 Muscular dystrophy, limb-girdle, type 1e MalaCards C4085211 Pain distress question C1548483 Leishmaniasis vaccine HSDN C4084788 Have dizziness C0020538 Hypertensive disease HSDN C4085317 Diarrhea frequency C0032229 Pleural neoplasms HSDN C0020672 Body temperature decreased C1000483 Genus anemia HSDN C1579931 Depressed - symptom C0751587 Cadasil syndrome OrphaNet|HPO C4084726 Distress cough C0221757 Alpha 1-antitrypsin deficiency HSDN C0349588 Stature short C1306229 Dyschromatosis universalis MalaCards|HPO C4084769 Vomiting frequency C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0042928 Paralysis vocal cord C0460137 Push down or depress HSDN C0030975 Disorders perception C0740392 Infarction, middle cerebral artery HSDN C0026603 Motion sickness C0018801 Heart failure HSDN C0038002 Spleen enlargement C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0518090 Frequency of pain question C0024693 Mandible injury HSDN C1963170 Hypothermia adverse event C0585442 Osteosarcoma of bone HSDN C0036572 Convulsion C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C0162835 Hypopigmentation C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C0424755 Fever symptoms C0393639 Hashimoto's encephalitis MalaCards C0030193 Sense of pain C0007020 Carbon monoxide poisoning HSDN C0454644 Delayed language development C1859567 Bardet-biedl syndrome 9 HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0700095 Central neuroblastoma HSDN C0015230 Exanthem C0276108 Chlamydia infection psittaci MalaCards C0040264 Ear ringing sound C0006663 Calcinosis HSDN C4084727 Cough frequency C0032310 Pneumonia, viral HSDN C2237041 Shox gene with short stature C3810100 Fanconi renotubular syndrome 3 MalaCards C0036572 Convulsion C0002949 Aneurysm, dissecting HSDN C3274924 Have been coughing C0027055 Myocardial reperfusion injury HSDN C0242936 Center pain C0021359 Infertility HSDN C4084723 Constipation C0001529 Dercum disease MalaCards C0013404 Respiratory difficulty C1336175 Stage iib adenosquamous cell carcinoma of lung UMLS C0007758 Cerebellar ataxia C0268393 Familial cerebral amyloid angiopathy HSDN C0018772 Deafness C2984291 Glioblastoma multiforme pathway HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1961100 Erectile dysfunction adverse event HSDN C0026821 Cramp C0026975 Myelitis HSDN C1962972 Proteinuria adverse event C0272295 Purpura, rheumatica MalaCards C3541349 Syncope C2827407 Infectious otitis media HSDN C0085593 Chill C0015556 Fallopian tube diseases HSDN C0518090 Frequency of pain question C3163620 Hypotension adverse event HSDN C4084767 Bothered by vomiting C0031069 Familial mediterranean fever HSDN C2096293 Ent surgical result ear vertigo C0016658 Fracture bone HSDN C0086565 Liver function abnormal C3808920 Anemia, hypochromic microcytic, with iron overload 2 MalaCards C4020887 Photodysphoria C0035613 Rift valley fever OrphaNet|MalaCards C0040034 Thrombocytopenia C3888244 Aicardi-goutieres syndrome 7 MalaCards C1963091 Diarrhea adverse event C0036093 Salivary gland diseases HSDN C0042025 Urinary incontinence stress C0009450 Disease caused by microorganism HSDN C0013428 Painful urination C0041974 Urethral stricture HSDN C0009676 Confusion state C0752332 Lupus vasculitis, central nervous system HSDN C0020305 Fetal edema C3278138 Fibrochondrogenesis 1 MalaCards C0038506 Stutter C0004275 Attitude health HSDN C0020672 Body temperature decreased C0022408 Arthropathy HSDN C2132198 Abnormal blistering of the skin C0042111 Urticaria pigmentosa MalaCards C1963170 Hypothermia adverse event C0024115 Lung diseases HSDN C1838869 Proximal neurogenic muscle weakness C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards|HPO C0018681 Headache, cephalalgia C0037199 Sinusitis UMLS C0851578 Disorder sleep C0023974 Loneliness HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035042 Psychology and religion HSDN C0518090 Frequency of pain question C2985290 Fetal alcohol spectrum disorders HSDN C0018991 Paralysis one side of body C0017510 Gestures HSDN C4084775 Usual severity weight loss C0043253 Trauma blunt HSDN C0424755 Fever symptoms C0023510 Leukocyte disorders HSDN C0518090 Frequency of pain question C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C0032617 High urine output C0020545 Hypertension, renovascular HSDN C0011991 Loose stools C0524620 Metabolic syndrome x HSDN C0003811 Cardiac rhythm disturbance C0796179 Teebi syndrome MalaCards C4084774 Have weight loss C3668816 Inflammation of non-human mammary gland HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0039101 Synovial sarcoma HSDN C0012833 Dizzy C0038579 Substance abuse, intravenous HSDN C3898969 Have been vomiting C0152164 Cyclical vomiting syndrome (disorder) MalaCards C0030193 Sense of pain C1963090 Dehydration adverse event HSDN C0015672 Decreased energy C0340629 Aortic aneurysm without mention of rupture nos HSDN C0037771 Paraparesis spastic C3550973 Neurodegeneration with brain iron accumulation 5 UMLS C0234132 Pyramidal sign C3810080 Mental retardation, autosomal recessive 40 MalaCards|UMLS C4085548 Usual severity dizziness C1956346 Coronary artery disease HSDN C0700078 Deep tendon reflex decrease C3494506 Pseudohypoparathyroidism, type ia HPO C4085317 Diarrhea frequency C0018378 Guillain-barre syndrome HSDN C0917816 Deficiency mental C0265342 Cerebrocostomandibular syndrome OrphaNet|HPO|MalaCards C0231218 Malaise generalized C1707406 Clear cell intrahepatic cholangiocarcinoma UMLS C2911647 Weight gain adverse event C0043168 Whooping cough due to unspecified organism HSDN C0015672 Decreased energy C0018571 Hand injury HSDN C1962972 Proteinuria adverse event C0020542 Pulmonary hypertension HSDN C0023380 Lethargy C1855115 Methylmalonic aciduria, mut(0) type HPO C3641756 Have diarrhea C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO C1963281 Vomiting adverse event C0027663 Neoplasms, multiple primary HSDN C0015672 Decreased energy C1829703 Carnitine palmitoyl transferase 1a deficiency OrphaNet|HPO C0518090 Frequency of pain question C0008495 Chorioamnionitis HSDN C0851578 Disorder sleep C0020649 Hypotension HSDN C2315100 Pediatric failure to thrive C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0035229 Respiratory function impaired C0003490 Aortic arch syndrome MalaCards C0522224 Palsied C1261470 Congenital meningocele HSDN C1384666 Decreased hearing C1552262 Nurse practitioner - family HSDN C0156308 Penis edema C0554315 Other male genital dis. nos UMLS C1145670 Failure respiratory C1838120 Hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities OrphaNet|MalaCards C0522224 Palsied C1690964 Cataract HSDN C1963093 Dizziness adverse event C0151744 Myocardial ischemia HSDN C0522224 Palsied C0041234 Chagas disease HSDN C0030193 Sense of pain C0259782 Telangiectatic osteosarcoma UMLS C2132198 Abnormal blistering of the skin C0343064 Keratolysis exfoliativa OrphaNet|MalaCards C3463815 Feel fatigue C0032285 Pneumonia HSDN C0233514 Behavior abnormal C1856059 Mthfr deficiency, thermolabile type HPO C3146279 Coma C0010074 Coronary vessel anomalies HSDN C0848203 Male pelvic pain C0014179 Endometritis HSDN C0030193 Sense of pain C2936664 Acquired hypogammaglobulinemia HSDN C0042963 Symptoms vomiting C0013010 Cerebral lateralization HSDN C4084776 Weight loss C0024141 Lupus erythematosus, systemic HSDN C0030193 Sense of pain C0040954 Infection by trichuris trichiura HSDN C4084766 Vomiting C0013182 Drug allergy HSDN C0024032 Birth weight subnormal C1857558 Hsd11b2, arg279cys HPO C4084775 Usual severity weight loss C0017689 Glucagonoma OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0002871 Anemia HSDN C3887638 Failure to thrive in infant C0035934 Rubinstein-taybi syndrome MalaCards|HSDN|HPO C0005745 Blepharoptosis C1853249 Spinocerebellar ataxia 28 MalaCards|HPO C0036572 Convulsion C4041181 Refractory infantile spasms co-occurrent with status epilepticus UMLS C4084767 Bothered by vomiting C0014236 Endophthalmitis HSDN C0349588 Stature short C2676137 Diamond-blackfan anemia 1 MalaCards|HPO C0041657 Consciousness loss C0456892 Csf low pressure HSDN C3541349 Syncope C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C4084776 Weight loss C0015773 Felty syndrome OrphaNet|MalaCards C0020649 Blood pressure decreased C3714602 Staphylococcal toxic shock syndrome MalaCards C0037763 Spasm C0019112 Hemorrhoids HSDN C4084776 Weight loss C0162624 Enoplida infection HSDN C0042963 Symptoms vomiting C1527348 Brain hypoxia HSDN C4085661 Usual severity nausea C0453996 Tobacco smoking HSDN C0038868 Supranuclear palsy progressive C0006118 Brain neoplasms HSDN C3898969 Have been vomiting C0017612 Glaucoma, open-angle HSDN C0518090 Frequency of pain question C0162316 Iron deficiency anemia HSDN C4084766 Vomiting C0032927 Precancerous conditions HSDN C0042571 Vertigo subjective C0087012 Ataxia, spinocerebellar HSDN C0042571 Vertigo subjective C0162872 Aortic aneurysm, thoracic HSDN C3641756 Have diarrhea C0033289 Family relationship, professional HSDN C0013421 Dystonia C0022336 Creutzfeldt-jakob disease HSDN C0018784 Deafness sensorineural C0035243 Respiratory tract infections HSDN C1384666 Decreased hearing C1832431 Digeorge syndrome-velocardiofacial syndrome complex 2 OrphaNet|MalaCards C0020673 Hypothermia (central) (local) C0011606 Exfoliative dermatitis HSDN C3887873 Hearing loss C1861391 Symphalangism with multiple anomalies of hands and feet MalaCards C0033774 Skin pruritus C0017181 Gastrointestinal hemorrhage HSDN C3898969 Have been vomiting C1963211 Pericarditis adverse event HSDN C0042024 Urine incontinence C0025286 Meningioma MalaCards C3541349 Syncope C1841658 Progressive familial heart block, type ii MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0022575 Keratoconjunctivitis sicca HSDN C4084768 Usual severity vomiting C0025521 Inborn errors of metabolism HSDN C1963180 Neck pain adverse event C0021799 Interprofessional relations HSDN C0036572 Convulsion C1864872 Spondyloepimetaphyseal dysplasia, genevieve type MalaCards C2700617 Irritation - emotion C0236642 Pick disease of the brain HPO C3463815 Feel fatigue C2930674 Babesioses, human MalaCards C0557874 Global developmental delay C4014414 Mental retardation, autosomal dominant 24 MalaCards C0019521 Hiccoughs C0043019 Lateral medullary syndrome HSDN C1838869 Proximal neurogenic muscle weakness C1837342 Muscular dystrophy, limb-girdle, type 2j MalaCards|HPO C0019079 Bloody sputum C0009186 Coccidioidomycosis HSDN C0162298 Stiffness joints C1846843 Epiphyseal dysplasia, multiple, 5 OrphaNet|HPO|MalaCards C0009763 Conjunctiva inflammation C0035920 Rubella DiseaseOntology|MalaCards C0018991 Paralysis one side of body C0041296 Tuberculosis HSDN C0042571 Vertigo subjective C0017638 Glioma HSDN C2984058 Have pain C0023283 Leishmaniasis, cutaneous HSDN C0041657 Consciousness loss C0004238 Atrial fibrillation HSDN C0018989 Paresis of one side of body C0006118 Brain neoplasms UMLS C2315100 Pediatric failure to thrive C0034341 Pyruvate carboxylase deficiency disease HSDN C0013362 Dysarthrias C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0036572 Convulsion C0751674 Lymphangioleiomyomatosis MalaCards|HPO C0036572 Convulsion C0026785 Munchhausen syndrome HSDN C0577979 Expectoration, frothy C3714582 Pneumonitis chemical MalaCards C4084802 Usual severity diarrhea C1962971 Myocarditis adverse event HSDN C1963071 Back pain adverse event C1546533 Specimen source codes - abscess HSDN C3670462 Pustular dermatitis C0011603 Dermatitis UMLS C2032396 Pelvic pain on the right C1881674 Medical device emits smoke HSDN C0033774 Skin pruritus C0006845 Candidiasis, chronic mucocutaneous MalaCards|HPO C0042963 Symptoms vomiting C0011854 Diabetes mellitus, insulin-dependent HSDN C1962972 Proteinuria adverse event C0037937 Spine injury HSDN C0026838 Spasticity muscle C0018213 Graves disease HSDN C0018772 Deafness C0022876 Premature obstetric labor HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C0018772 Deafness C0009240 Cognition HSDN C4084725 Usual severity cough C0022758 Kap HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0149520 Acute cholecystitis HSDN C0020672 Body temperature decreased C0022716 Menkes kinky hair syndrome MalaCards|HSDN|HPO C1963093 Dizziness adverse event C0007020 Carbon monoxide poisoning HSDN C0150055 Pain chronic C1623041 Breast-fed HSDN C4085222 Nausea C0027686 Pathologic neovascularization HSDN C1000483 Genus anemia C0549143 Pulmonary renal syndrome MalaCards C2984058 Have pain C0339289 Injury corneal HSDN C4050613 Anxiety C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C1962972 Proteinuria adverse event C4050613 Anxiety scale (basc-2) HSDN C1963249 Tinnitus adverse event C0042769 Virus diseases HSDN C1963071 Back pain adverse event C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C0009806 Constipate C1263846 Attention deficit hyperactivity disorder HSDN C1549543 Administration method - pain C0220981 Metabolic acidosis HSDN C0030486 Extremity paralysis, lower C0042345 Varicosity HSDN C4084766 Vomiting C0887833 Carcinoma, pancreatic ductal HSDN C0024031 Back pain lower back C0017178 Gastrointestinal diseases HSDN C2237041 Shox gene with short stature C0524582 Mulibrey nanism OrphaNet|HPO|MalaCards C4085210 Usual severity pain C1861172 Venous thromboembolism HSDN C0042798 Vision dim C0265223 Cohen syndrome HPO C0040822 D tremors C0023418 Leukemia HSDN C4084727 Cough frequency C0023241 Legionnaires' disease OrphaNet|MalaCards C1963091 Diarrhea adverse event C0023891 Liver cirrhosis, alcoholic HSDN C0231528 Muscle pain generalized C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C4084727 Cough frequency C0007133 Carcinoma, papillary HSDN C4084767 Bothered by vomiting C0013288 Dumping syndrome HSDN C0015970 Fever unknown origin C0019699 Hiv seropositivity HSDN C1962972 Proteinuria adverse event C0028738 Nystagmus HSDN C2024878 Cardiovascular surgery result: dyspnea C1836122 Sarcoidosis, early-onset MalaCards C4084767 Bothered by vomiting C1135868 Gestational trophoblastic neoplasms HSDN C0086437 Joint hypermobility C0018522 Hallermann's syndrome MalaCards C0085636 Light sensitivity C2750065 Retinitis pigmentosa, juvenile, lrat-related HPO C1963087 Constipation adverse event C1834211 Ganglioneuromatosis of the alimentary tract HPO C0013421 Dystonia C1843014 Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques HPO C0497406 Over weight C0233629 Thinking and speaking disturbances HSDN C0036572 Convulsion C0035920 Rubella HSDN C0030193 Sense of pain C3160917 Bladder pain syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0032994 Pregnancy, tubal HSDN C0423708 Obturator neuralgia C4075727 Post-surgery obturator neuralgia UMLS C4084723 Constipation C0085278 Antiphospholipid syndrome HSDN C0011570 Monopolar depression C0162532 Variegate porphyria MalaCards|HPO C3898969 Have been vomiting C0018916 Hemangioma HSDN C0011991 Loose stools C0010038 Corneal opacity HSDN C0413252 Hypothermia due to exposure C0003507 Aortic valve stenosis HSDN C3887638 Failure to thrive in infant C3553960 Peroxisome biogenesis disorder 8b MalaCards C0232695 Bowel sound decreased C1335686 Neuroendocrine neoplasm of rectum MalaCards C3463815 Feel fatigue C0010068 Coronary heart disease HSDN C0020455 Hypergammaglobulinemia C0149745 Oral ulcer HSDN C0013604 Edematous C3540851 Nci ctep sdc chondrosarcoma sub-category terminology HSDN C0557874 Global developmental delay C1855645 Keratoconus posticus circumscriptus MalaCards C2032396 Pelvic pain on the right C2984289 Melanoma pathway HSDN C3641756 Have diarrhea C0009663 Condylomata acuminata HSDN C0015672 Decreased energy C0029463 Osteosarcoma HSDN C0221263 Cafe au lait spot C0206727 Nerve sheath tumors HSDN C0005745 Blepharoptosis C1859468 Bird headed dwarfism montreal type OrphaNet|MalaCards C0231528 Muscle pain generalized C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|HPO|MalaCards C0013421 Dystonia C1868675 Parkinson disease 2, autosomal recessive juvenile HPO C2029884 Hearing loss by exam C0008625 Chromosome aberrations HSDN C0036572 Convulsion C0027645 Neoplasm seeding HSDN C2029884 Hearing loss by exam C0027407 Narcotherapy HSDN C0020538 Hbp C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|HPO|MalaCards C4085211 Pain distress question C0005119 Bereavement HSDN C0349588 Stature short C1836123 Goldberg-shprintzen megacolon syndrome OrphaNet|HPO C1963086 Confusion adverse event C0018839 Heat exhaustion HSDN C0270795 Monopareses C0856327 Left arm paresis UMLS C1963170 Hypothermia adverse event C0003469 Anxiety disorders HSDN C0026205 Pupillary constriction C0338586 Vertebral artery dissection HSDN C4084767 Bothered by vomiting C0043241 Wound infection HSDN C0557874 Global developmental delay C0268467 Hyperphenylalaninemia, bh4-deficient, b MalaCards|HPO C4085862 Bothered by nausea C0236969 Substance-related disorders HSDN C0010038 Corneal opacity disorder C0544008 Chandler syndrome MalaCards C1963086 Confusion adverse event C0023890 Liver cirrhosis HSDN C0851578 Disorder sleep C0007787 Transient ischemic attack HSDN C4084725 Usual severity cough C0152264 Familial erythrocytosis HPO C0030193 Sense of pain C0042214 Vaccinia HSDN C0004134 Dyssynergia C0497327 Dementia MalaCards C0019209 Large liver C2673914 Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive MalaCards C0030193 Sense of pain C0477378 Vascular headache, nec in snomedct UMLS C4085211 Pain distress question C0042267 Vaginitis HSDN C1519353 Skin eruption papular C0398597 Histiocytic syndrome MalaCards C0027066 Myoclonic jerking C0005695 Bladder neoplasm HSDN C1963065 Apnea adverse event C0025312 Meningomyelocele HSDN C0007758 Cerebellar ataxia C0038663 Suicide attempt HSDN C0023015 Language handicap C1096903 Sialic acid storage disease, finnish type (disorder) HSDN C4085551 Usual severity dry mouth C0014805 Primary erythermalgia MalaCards C0042963 Symptoms vomiting C0009946 Conversion disorder HSDN C0013404 Respiratory difficulty C3163620 Hypotension adverse event HSDN C2984058 Have pain C0751774 Nocturnal myoclonus syndrome HSDN C0151889 Reflexes tendon increased C1858535 Microcephaly, primary autosomal recessive, 2 (disorder) MalaCards|HPO C0751495 Seizure focal C0474327 Partial seizure evolving to secondary generalised seizure UMLS C0039070 Collapse fleeting C0026640 Mouth neoplasms HSDN C2911647 Weight gain adverse event C3888013 Hypnoses HSDN C0042963 Symptoms vomiting C0020701 Somatization disorder HSDN C4084784 Diarrhea C0033700 Infection proteus HSDN C0036572 Convulsion C0021053 Immune system diseases HSDN C3887638 Failure to thrive in infant C4053775 Pituitary stalk interruption syndrome MalaCards C1961131 Cough adverse event C0006434 Burn injury HSDN C0013404 Respiratory difficulty C0027686 Pathologic neovascularization HSDN C0497247 Blood pressure elevation C0268146 Glucose-6-phosphate transport defect MalaCards|HPO C0013911 Emaciate C0346326 Optic nerve glioma HSDN C0013604 Edematous C0017612 Glaucoma, open-angle HSDN C2984058 Have pain C0036986 Shock, traumatic HSDN C3641756 Have diarrhea C0016509 Dermatoses, foot HSDN C0003469 Anxiety disorder C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C0011991 Loose stools C2697368 Gastrointestinal irritation UMLS C0000737 Abdomen pain C0271642 Fibrocalculous pancreatic diabetes MalaCards C0018681 Headache, cephalalgia C0029139 Optical illusion HSDN C0013604 Edematous C0034013 Precocious puberty HSDN C1557397 Adverse event associated with pain C0022570 Keratitis dentritic HSDN C4084767 Bothered by vomiting C1962958 Hematoma adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0393735 Headache disorders HSDN C0015672 Decreased energy C0023891 Liver cirrhosis, alcoholic HSDN C3641755 Have constipation C0029456 Osteoporosis HSDN C0727671 Red cross toothache drops C0031106 Periodontitis, juvenile HSDN C0040822 D tremors C0029294 Orofaciodigital syndromes MalaCards C0018524 Hallucinate C0019196 Hepatitis c HSDN C0518090 Frequency of pain question C0022638 Ketosis HSDN C0700200 Presyncope C0042420 Vasovagal syncope UMLS C3815497 Cough C0029456 Osteoporosis HSDN C0241210 Speaking delay C2931482 Neurofibromatosis-noonan syndrome MalaCards|HPO C4085862 Bothered by nausea C0042345 Varicosity HSDN C0000727 Abdomen acute C0038940 Surgical wound dehiscence HSDN C0020455 Hypergammaglobulinemia C0011603 Dermatitis HSDN C4042891 Sleep wake disorders C0018799 Heart diseases HSDN C0242936 Center pain C0041234 Chagas disease HSDN C0027066 Myoclonic jerking C2673635 Combined saposin deficiency MalaCards|HPO|UMLS C4084766 Vomiting C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0002170 Alopecia disorders C0175692 Johanson-blizzard syndrome OrphaNet|HPO|MalaCards C0013528 Echo speech C0008066 Child behavior disorders HSDN C2911645 Weight loss adverse event C0032533 Polymyalgia rheumatica MalaCards C3163620 Hypotension adverse event C0265836 Congenital tricuspid valve stenosis MalaCards C0000737 Abdomen pain C0585274 Periodic syndrome OrphaNet|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0037413 Social dominance HSDN C1069915 Vertigo C0039483 Giant cell arteritis MalaCards|HPO C0036572 Convulsion C0013502 Echinococcosis HSDN C4084723 Constipation C0007193 Cardiomyopathy, dilated HSDN C0557874 Global developmental delay C0220658 Pfeiffer syndrome MalaCards C0038002 Spleen enlargement C1856476 Gaucher disease, type iiic OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0278510 Medulloblastoma, childhood UMLS C4084784 Diarrhea C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0016382 Cutaneous vascular engorgement C0014805 Primary erythermalgia MalaCards C0013395 Indigestion C3714514 Infection HSDN C4084769 Vomiting frequency C1705810 Generic role HSDN C0016382 Cutaneous vascular engorgement C0162819 Skin diseases, vascular UMLS C4084766 Vomiting C0019209 Hepatomegaly HSDN C0030232 Color loss C3889576 Euphoria HSDN C0013604 Edematous C0013312 Dupuytren contracture HSDN C0574002 Foot swelling C0023891 Liver cirrhosis, alcoholic UMLS C2203646 Jaundice C0034063 Pulmonary edema HSDN C3887638 Failure to thrive in infant C1848561 Methylmalonic acidemia with homocystinuria OrphaNet|HPO|MalaCards C4084784 Diarrhea C0007124 Noninfiltrating intraductal carcinoma HSDN C3541349 Syncope C2678478 Brugada syndrome 3 MalaCards|HPO C1549543 Administration method - pain C0221757 Alpha 1-antitrypsin deficiency HSDN C0036572 Convulsion C4014545 Tatton-brown-rahman syndrome MalaCards C0231218 Malaise generalized C0279606 Childhood hepatocellular carcinoma UMLS C0039870 Leanness C0033860 Psoriasis HSDN C0839480 Leg lower pain C0020579 Hypervitaminosis a MalaCards C3274924 Have been coughing C1175175 Severe acute respiratory syndrome HSDN C0917816 Deficiency mental C0796038 Mcdonough syndrome OrphaNet|MalaCards C3898969 Have been vomiting C0032969 Pregnancy in diabetics HSDN C1962972 Proteinuria adverse event C1963083 Cholecystitis adverse event HSDN C0018772 Deafness C0013080 Down syndrome HSDN C0030193 Sense of pain C1445886 Myalgia/myositis of neck UMLS C0011206 Delirium acute C0023418 Leukemia HSDN C0019572 Hairiness C0020564 Hypertrophy HSDN C3641756 Have diarrhea C0032002 Pituitary diseases HSDN C0010200 Cough symptom C0041755 Adverse reaction to drug HSDN C4084788 Have dizziness C3714644 Thymus neoplasms HSDN C0426579 Anorexia symptom C0011989 Camurati-engelmann syndrome MalaCards|HPO C3887873 Hearing loss C0001973 Alcoholic intoxication, chronic HSDN C0040460 Dental pain C0007222 Cardiovascular diseases HSDN C0085632 Listlessness C2677565 Amyotrophic lateral sclerosis 10 (disorder) HPO|UMLS C0013428 Painful urination C1997249 Neuralgia, pudendal MalaCards C3898969 Have been vomiting C1833511 Carnitine palmitoyltransferase ii deficiency, infantile HPO C0035078 Failure kidney C0002986 Fabry disease OrphaNet|HPO|MalaCards C3665386 Abnormal vision C1568247 Usher syndrome, type i HPO C0018784 Deafness sensorineural C0085298 Sudden cardiac death HSDN C0037384 Snore C0020538 Hypertensive disease HSDN C4084726 Distress cough C3541306 Plasmodium measurement HSDN C0020673 Hypothermia (central) (local) C2930798 Alexanders leukodystrophy MalaCards C0027497 Queasy C1550639 Specimen type - fistula HSDN C0013362 Dysarthrias C1834659 Muscular dystrophy, limb-girdle, type 1a MalaCards C0587246 Extremity weakness C0003803 Arnold chiari malformation MalaCards C4084724 Usual severity constipation C0042029 Urinary tract infection HSDN C0848203 Male pelvic pain C2350572 Illness behavior HSDN C1963281 Vomiting adverse event C0033289 Family relationship, professional HSDN C0015672 Decreased energy C0040100 Thymoma OrphaNet|MalaCards C0020580 Decreased sensation C0009375 Colonic neoplasms HSDN C0011168 Disorder deglutition C1866785 Spheroid body myopathy MalaCards|HPO C2919142 Short stature adverse event C0015625 Fanconi anemia OrphaNet|HPO|MalaCards C0917816 Deficiency mental C0265223 Cohen syndrome OrphaNet|HPO C1961131 Cough adverse event C0011981 Diaphragmatic eventration HSDN C4084776 Weight loss C0028758 Bonding HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0001418 Adenocarcinoma HSDN C0037383 Sneeze C0021400 Influenza HSDN C1557397 Adverse event associated with pain C0019202 Hepatolenticular degeneration HSDN C0240715 Perineal lump C0347500 Benign neopl bartholin's gland UMLS C4084776 Weight loss C3714644 Thymus neoplasms MalaCards|HSDN C3539889 Pelvic pain increasing in severity C0004935 Animal ethology HSDN C0004134 Dyssynergia C1707400 Classic medulloblastoma MalaCards C3541349 Syncope C0007134 Renal cell carcinoma HSDN C0008031 Pain chest C0031048 Pericarditis, constrictive HSDN C0751265 Learning disability C1858054 Bardet-biedl syndrome 6 MalaCards C1961131 Cough adverse event C0206613 Paramyxoviridae infections HSDN C1519353 Skin eruption papular C1274789 Ligneous conjunctivitis MalaCards|HPO C0242936 Center pain C0023869 Lithiasis HSDN C1999266 Depression adverse event C0001622 Adrenal gland hyperfunction OrphaNet C0413252 Hypothermia due to exposure C0020659 Hypothalamic neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0009400 Colorado tick fever DiseaseOntology|MalaCards C0009806 Constipate C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C1963170 Hypothermia adverse event C0018671 Head and neck neoplasms HSDN C0030552 Paralysis partial C0948264 Neuroborreliosis MalaCards C0035232 Diaphragmatic paralysis C1322286 Thymoma, type c OrphaNet|MalaCards C0027497 Queasy C0042830 Perception visual HSDN C2096293 Ent surgical result ear vertigo C0027627 Neoplasm metastasis HSDN C4085210 Usual severity pain C3249881 Infection - suppurative HSDN C0009806 Constipate C3897517 Stage ivb colon cancer UMLS C4085661 Usual severity nausea C0162565 Acute intermittent porphyria MalaCards|HPO C0042963 Symptoms vomiting C0162576 Anisakiasis HSDN C0423818 Grooving of nail C0220767 Craniofrontonasal dysplasia UMLS C3539890 Pelvic pain causes awakening at night C0037929 Spinal cord injuries HSDN C3463815 Feel fatigue C0041948 Uremia HSDN C0018772 Deafness C0028433 Nose neoplasms HSDN C4084768 Usual severity vomiting C0027659 Neoplasms, experimental HSDN C4084775 Usual severity weight loss C0027932 Neurotic disorders HSDN C3898969 Have been vomiting C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0231218 Malaise generalized C1708717 Localized resectable adult hepatocellular carcinoma UMLS C2096293 Ent surgical result ear vertigo C2586211 Thrombosis of blood vessel HSDN C1557397 Adverse event associated with pain C0004114 Astrocytoma HSDN C0004134 Dyssynergia C0007273 Carotid artery diseases HSDN C3274924 Have been coughing C0276108 Chlamydia infection psittaci HSDN C0013604 Edematous C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0162834 Hyperpigmentation C2931617 Bahemuka brown syndrome MalaCards C0018681 Headache, cephalalgia C0162316 Iron deficiency anemia HSDN C2096293 Ent surgical result ear vertigo C0162872 Aortic aneurysm, thoracic HSDN C0027498 Nausea vomiting C0010418 Cryptosporidiosis DiseaseOntology C0011991 Loose stools C0018378 Guillain-barre syndrome HSDN C0018991 Paralysis one side of body C0019069 Hemophilia a HSDN C4084767 Bothered by vomiting C0265673 Congenital kyphosis HSDN C0557874 Global developmental delay C0268353 Cutis laxa, x-linked MalaCards C0850758 Pain pelvic C1704436 Peripheral arterial diseases HSDN C0018772 Deafness C0029878 Otitis externa HSDN C0039070 Collapse fleeting C1970119 Cardiac arrhythmia, ankyrin-b-related MalaCards|HPO|UMLS C1963137 Hydrocephalus adverse event C0265245 Nager syndrome MalaCards|HPO C4085661 Usual severity nausea C0033923 Psychomotor function HSDN C0030552 Paralysis partial C1847839 Episodic ataxia, type 3 MalaCards C0042024 Urine incontinence C0221752 Rbc urine HSDN C0162298 Stiffness joints C1444199 Alkaptonuric ochronosis MalaCards C0221166 Paraparesis C0014175 Endometriosis HSDN C0001707 Aerophagia C0038536 Subcutaneous emphysema HSDN C0151786 Weakness muscle C0037047 Sibling HSDN C0086565 Liver function abnormal C1970196 Mental retardation, autosomal recessive 8 MalaCards C0015970 Fever unknown origin C0009782 Connective tissue diseases HSDN C0234979 Dysdiadochokinesia C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO|UMLS C0018780 Frequencies hearing high loss C0206504 Tympanic membrane perforation HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026948 Mycosis fungoides HSDN C0917816 Deficiency mental C1845136 Chromosome xp11.3 deletion syndrome MalaCards C1963077 Bone pain adverse event C3896673 Familial nonmedullary thyroid gland carcinoma MalaCards C0398650 Idiopathic thrombocytopenia purpura C0043194 Wiskott-aldrich syndrome HSDN C0578044 Ear painful C0017409 Herpes zoster oticus UMLS C0020578 Hyperventilate C2984289 Melanoma pathway HSDN C0009398 Color vision defects C1842475 Retinitis pigmentosa 7 MalaCards C2984058 Have pain C0016548 Foreign body migration HSDN C4084784 Diarrhea C0037356 Smallpox virus HSDN C0349588 Stature short C1859965 Alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus MalaCards C0013608 Cardiac edema C1963090 Dehydration adverse event HSDN C0008031 Pain chest C0413723 Ibuprofen adverse reaction UMLS C4084723 Constipation C4084909 Depression subordinate domain HSDN C0030200 Intractable pain C0004935 Animal ethology HSDN C1963091 Diarrhea adverse event C0029106 Opisthorchiasis DiseaseOntology C3815497 Cough C0003493 Aortic diseases HSDN C0014724 Burping C3489393 Hiatal hernia HSDN C2203646 Jaundice C0153459 Malignant neoplasm of body of pancreas MalaCards C0085128 Cardiac output elevated C0243026 Sepsis HSDN C0746674 Muscle weakness generalized C0342751 Generalized glycogen storage disease of infants MalaCards C0013404 Respiratory difficulty C0345904 Malignant neoplasm of liver MalaCards C0015230 Exanthem C1276072 Adult atopic dermatitis UMLS C0751840 Pure alexia C0009928 Contrast sensitivity HSDN C0042963 Symptoms vomiting C0031039 Effusion pericardial HSDN C0009421 Comatose C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0041834 Erythematous condition C1851480 Greither disease OrphaNet|HPO C4084775 Usual severity weight loss C0020725 Type ii mucolipidosis MalaCards|HPO C0015468 Face pain C1762616 Meningioma, benign, no icd-o subtype HSDN C0018681 Headache, cephalalgia C0376532 Epilepsy, rolandic HSDN C0013604 Edematous C0024796 Marfan syndrome HSDN C0522224 Palsied C0344435 Ventricular fibrillation by ecg finding HSDN C0242936 Center pain C0023269 Leiomyosarcoma HSDN C3146279 Coma C0002351 Altitude sickness HSDN C0018681 Headache, cephalalgia C0022410 Joint instability HSDN C2919142 Short stature adverse event C1844375 Gynecomastia, familial MalaCards C0007815 Cerebrospinal fluid rhinorrhoea C0036690 Septicemia HSDN C1549543 Administration method - pain C0334533 Arteriovenous hemangioma HSDN C4084726 Distress cough C0018824 Heart valve disease HSDN C3274924 Have been coughing C0085073 Prosthesis-related infection HSDN C4085548 Usual severity dizziness C0023890 Liver cirrhosis HSDN C0035229 Respiratory function impaired C2931854 Allergic bronchopulmonary mycosis MalaCards C0042024 Urine incontinence C0007453 Cattle disease HSDN C4085210 Usual severity pain C0015404 Eye infections, bacterial HSDN C2911645 Weight loss adverse event C0023904 Liver neoplasms, experimental HSDN C2024878 Cardiovascular surgery result: dyspnea C0242216 Biliary calculi HSDN C0020672 Body temperature decreased C0025289 Meningitis HSDN C0030554 Abnormal sensation C1868649 Panic disorder 1 HSDN C3539893 Pelvic pain occurs with intercourse C0017416 Genital neoplasms, female HSDN C0019209 Large liver C0085548 Autosomal recessive polycystic kidney disease HPO C0151827 Pain eye C1704421 Skin pigmentation disorder HSDN C1963180 Neck pain adverse event C0029456 Osteoporosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162637 Strongylida infections HSDN C3463815 Feel fatigue C0031154 Peritonitis HSDN C2029884 Hearing loss by exam C1290398 Cerebral arterial aneurysm HSDN C0019214 Hepatosplenomegaly C0042782 Visceromegaly UMLS C4085642 Level of joint stiffness C1327918 Oculootoradial syndrome MalaCards C0151818 Opisthotonos C2749560 Methemoglobinemia, type ii HPO C0085631 Abnormal excitement C0242422 Parkinsonian disorders HSDN C2242996 Tingling C0041327 Tuberculosis, pulmonary HSDN C2984058 Have pain C0238015 Autonomic dysreflexia HSDN C0018681 Headache, cephalalgia C1690964 Cataract HSDN C0242936 Center pain C0017152 Gastritis HSDN C1963065 Apnea adverse event C0003873 Rheumatoid arthritis HSDN C2911645 Weight loss adverse event C0001883 Airway obstruction HSDN C0242936 Center pain C1705811 Terminology role entity HSDN C0020305 Fetal edema C0037939 Spinal neoplasms HSDN C0030193 Sense of pain C0026613 Motor skills disorders HSDN C4084767 Bothered by vomiting C1546847 Entity name part type - family HSDN C4084767 Bothered by vomiting C0016053 Fibromyalgia HSDN C3539022 Pelvic pain decreasing in severity C0029456 Osteoporosis HSDN C1549543 Administration method - pain C0005891 Bodies image HSDN C2984058 Have pain C0007798 Cerebral ventricle neoplasm HSDN C0349588 Stature short C1852542 Cdo syndrome MalaCards C0030554 Abnormal sensation C0023798 Lipoma HSDN C0013421 Dystonia C3810285 Myopathy with extrapyramidal signs MalaCards C0020455 Hypergammaglobulinemia C0206141 Idiopathic hypereosinophilic syndrome HSDN C1069915 Vertigo C0029443 Osteomyelitis HSDN C0030552 Paralysis partial C0006264 Bronchial neoplasms HSDN C4084767 Bothered by vomiting C0027627 Neoplasm metastasis HSDN C4084784 Diarrhea C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0015230 Exanthem C0740933 Alumina/magnesia adverse reaction UMLS C0024032 Birth weight subnormal C4015610 Chromosome 11p11.2 deletion syndrome, 91.3-kb MalaCards C0007859 Pain neck C0018799 Heart diseases HSDN C3539889 Pelvic pain increasing in severity C0007527 Cecal disease HSDN C0038990 Sweats C0003490 Aortic arch syndrome MalaCards C3887873 Hearing loss C0079744 Diffuse large b-cell lymphoma HSDN C0023012 Delay language C4015167 Mental retardation, autosomal dominant 30 MalaCards C4085549 Dizziness C0038358 Gastric ulcer HSDN C0150055 Pain chronic C0702221 Tactual discrimination HSDN C2242996 Tingling C0029172 Oral submucous fibrosis HSDN C0036572 Convulsion C3266633 Temporal lobe epilepsy with mesial temporal sclerosis UMLS C0086565 Liver function abnormal C3809522 Infantile liver failure syndrome 1 MalaCards C1963087 Constipation adverse event C0517555 Venous thrombosis after immobility HSDN C2032395 Pelvic pain on the left C0018799 Heart diseases HSDN C4085210 Usual severity pain C0003490 Aortic arch syndrome HSDN C0039070 Collapse fleeting C0264903 Premature ventricular complex multifocal MalaCards C3898969 Have been vomiting C3241945 Melena due to gastrointestinal hemorrhage HSDN C0004604 Pain back C0033893 Tension headache HSDN C1549543 Administration method - pain C0012655 Disease susceptibility HSDN C3898969 Have been vomiting C1416865 Lipa gene HPO C0014591 Bleeding nose C0398641 Epstein syndrome (disorder) HPO C0007758 Cerebellar ataxia C0751783 Lafora disease HSDN C0221150 Odynophagia C0013595 Eczema UMLS C0003862 Pain joint C0917715 Hajdu-cheney syndrome OrphaNet|HPO C1963090 Dehydration adverse event C1864499 Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss HPO C1963281 Vomiting adverse event C0025160 Megacolon HSDN C1557397 Adverse event associated with pain C0436596 On examination - apathetic HSDN C1963180 Neck pain adverse event C0521169 Fracture compression HSDN C0013421 Dystonia C1845892 Hprt deficiency, neurologic variant HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0033873 Psychiatry HSDN C0012833 Dizzy C0009946 Conversion disorder HSDN C0019209 Large liver C0023787 Lipodystrophy MalaCards C2024878 Cardiovascular surgery result: dyspnea C0018939 Hematological disease HSDN C0398650 Idiopathic thrombocytopenia purpura C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0020673 Hypothermia (central) (local) C0013926 Aeroembolism HSDN C0013604 Edematous C0002991 Cutaneous fibrous histiocytoma HSDN C0030552 Paralysis partial C0175754 Agenesis of corpus callosum HSDN C2024893 Cardiovascular surgery result: fatigue C0034072 Cor pulmonale HSDN C0413252 Hypothermia due to exposure C0040046 Thrombophlebitis HSDN C2096293 Ent surgical result ear vertigo C0025284 Meningeal neoplasms HSDN C0004134 Dyssynergia C1839413 Pyruvate dehydrogenase e1 alpha deficiency MalaCards C0042798 Vision dim C0162809 Kallmann syndrome OrphaNet|HPO|MalaCards C3887873 Hearing loss C0033871 Psychiatric status rating scales HSDN C3274924 Have been coughing C0006272 Bronchiolitis obliterans HSDN C0004134 Dyssynergia C1848932 Tapetoretinal degeneration with ataxia MalaCards C0018777 Deafness, conductive C0027122 Myositis ossificans HSDN C1069915 Vertigo C0039984 Thoracic outlet syndrome HSDN C4084773 Bothered by weight gain C0270611 Brain damage HSDN C0036572 Convulsion C2931672 Cerebral hemorrhage with amyloidosis, hereditary, dutch type OrphaNet|HPO C4085317 Diarrhea frequency C1835888 Diarrhea 4, malabsorptive, congenital MalaCards|HPO C4084802 Usual severity diarrhea C0003860 Arteritis HSDN C0030193 Sense of pain C0037047 Sibling HSDN C0013428 Painful urination C0030849 Penile neoplasms HSDN C0042798 Vision dim C0752143 Intracranial thrombosis HSDN C0013911 Emaciate C0033300 Progeria HSDN C0011991 Loose stools C0037275 Skin diseases, vesiculobullous HSDN C0036572 Convulsion C1861172 Venous thromboembolism HSDN C1963091 Diarrhea adverse event C0282193 Iron overload HSDN C0009421 Comatose C0000833 Abscess HSDN C1549543 Administration method - pain C0085271 Self-injurious behavior HSDN C0027796 Neuralgias C1527429 Increased blood npn HSDN C0018772 Deafness C0010346 Crohn disease HSDN C0012569 Double vision C0019829 Hodgkin disease HSDN C3887873 Hearing loss C1522133 High cholesterol level HSDN C4084766 Vomiting C0032064 Plague HSDN C4085661 Usual severity nausea C0001883 Airway obstruction HSDN C3814530 Skin vesicle C0268323 Familial porphyria cutanea tarda MalaCards C0751093 Dystonia, limb C1860315 Whispering dysphonia, hereditary MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0349622 Hemangiopericytoma of meninges HSDN C0018681 Headache, cephalalgia C0206716 Ganglioglioma HSDN C1963091 Diarrhea adverse event C0008370 Cholestasis HSDN C0003862 Pain joint C1837657 Spondyloepiphyseal dysplasia, omani type MalaCards C1963180 Neck pain adverse event C0012644 Animal disease models HSDN C2881985 Diplacusis, right ear C0810000 Other ear and sense organ disorders UMLS C0018681 Headache, cephalalgia C1334645 Inverted papilloma of maxillary sinus UMLS C0038990 Sweats C0029434 Osteogenesis imperfecta OrphaNet C0018681 Headache, cephalalgia C0034065 Pulmonary embolism HSDN|UMLS C4084775 Usual severity weight loss C0020649 Hypotension HSDN C0032285 Pneum C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C0030193 Sense of pain C0236664 Alcohol-related disorders HSDN C4084766 Vomiting C1547044 Kind of quantity - smell HSDN C3898969 Have been vomiting C0006309 Brucellosis HSDN C0034150 Skin purpura C3495801 Granulomatosis with polyangiitis MalaCards|HPO C0030193 Sense of pain C0001197 Acrodermatitis HSDN C1557397 Adverse event associated with pain C0853697 Neutrophil count decreased HSDN C0018991 Paralysis one side of body C1832903 Migraine, sporadic hemiplegic HPO C0043094 Weight gain C0041582 Ulcer HSDN C0038002 Spleen enlargement C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C4084726 Distress cough C0001519 Adie holmes syndrome HSDN C0026838 Spasticity muscle C2751092 Neuropathy, hereditary sensory and autonomic, type iib MalaCards|HPO C0020672 Body temperature decreased C0035243 Respiratory tract infections HSDN C0042963 Symptoms vomiting C0745744 End stage liver disease UMLS C0043094 Weight gain C0026769 Multiple sclerosis HSDN C0019572 Hairiness C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C4084776 Weight loss C0042138 Uterine neoplasms HSDN C4084773 Bothered by weight gain C0018802 Congestive heart failure HSDN C3898969 Have been vomiting C0026936 Mycoplasma infections HSDN C0231528 Muscle pain generalized C0036421 Systemic scleroderma OrphaNet|MalaCards C0011206 Delirium acute C0004377 Automatism HSDN C0270948 Neurogenic muscular atrophy C2675491 Amyotrophic lateral sclerosis 11 MalaCards|HPO C0019572 Hairiness C0265293 Frontometaphyseal dysplasia HPO C0042025 Urinary incontinence stress C1527429 Increased blood npn HSDN C2911645 Weight loss adverse event C0853697 Neutrophil count decreased HSDN C3898969 Have been vomiting C0004161 Athletic injuries HSDN C2936821 Spinal cerebrospinal fluid leak C0037061 Siderosis HSDN C4084767 Bothered by vomiting C0085278 Antiphospholipid syndrome HSDN C2984058 Have pain C0043395 Yellow fever HSDN C0860603 Anxiety symptom C1527168 Bonnevie-ullrich syndrome MalaCards C0231835 Respiration rate increased C0014009 Empyema HSDN C1963086 Confusion adverse event C1962963 Osteoporosis adverse event HSDN C0004604 Pain back C1264008 Chronic cold agglutinin disease MalaCards C0030193 Sense of pain C0024021 Loudness perception HSDN C2054487 Teeth sensitive to both cold and heat C0011432 Dentin hypersensitivity UMLS C1279888 Proteinuria of undiagnosed cause C0010038 Corneal opacity HSDN C0021167 Incontinence nos C1839780 Fragile x tremor/ataxia syndrome MalaCards C3539022 Pelvic pain decreasing in severity C3887532 Ulceration HSDN C0027497 Queasy C0043124 West nile fever MalaCards C4084784 Diarrhea C0032708 Disorders of porphyrin metabolism OrphaNet|HSDN|MalaCards C0011991 Loose stools C3661523 Congenital intestinal aganglionosis MalaCards|HPO C3887638 Failure to thrive in infant C3150787 Chromosome 17q21.31 duplication syndrome MalaCards C0027497 Queasy C0017601 Glaucomas HSDN C0011206 Delirium acute C3714509 Nutrition disorders HSDN C0015672 Decreased energy C0022104 Irritable bowel syndrome HSDN C0003962 Ascites C0265268 Adams oliver syndrome MalaCards|HPO C0011991 Loose stools C0006663 Calcinosis HSDN C1963252 Tremor adverse event C0432443 Deletion of long arm of chromosome 18 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1258215 Ileus HSDN C0085606 Urination urgency C1846564 Spastic paraplegia 7, autosomal recessive MalaCards|HPO C0015230 Exanthem C0263224 Flexural atopic dermatitis UMLS C4085661 Usual severity nausea C0349464 Wernicke-korsakoff syndrome HSDN C0030193 Sense of pain C0017572 Gingival recession HSDN C1384666 Decreased hearing C1148551 X-linked dyskeratosis congenita MalaCards C4084766 Vomiting C0027794 Neural tube defects HSDN C0015230 Exanthem C0406641 Genital lichen sclerosus UMLS C3641755 Have constipation C0848377 Trauma to the abdomen HSDN C4084768 Usual severity vomiting C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C2029884 Hearing loss by exam C0026640 Mouth neoplasms HSDN C0026821 Cramp C0393576 Chorea acanthocytosis syndrome HSDN C0032617 High urine output C0031065 Perinephritis HSDN C4085548 Usual severity dizziness C0012691 Dislocations HSDN C2984058 Have pain C0272375 Antithrombin iii deficiency HSDN C0424755 Fever symptoms C0010073 Coronary artery vasospasm HSDN C0030200 Intractable pain C0751941 Glossopharyngeal nerve disease or syndrome HSDN C0042940 Disorder of voice C0019829 Hodgkin disease HSDN C0030232 Color loss C3888018 Congenital hyperinsulinism MalaCards C2024893 Cardiovascular surgery result: fatigue C0039082 Syndrome HSDN C4085211 Pain distress question C0020461 Hyperkalemia HSDN C0520909 Ponv C0032962 Pregnancy complications HSDN C4085210 Usual severity pain C0010072 Coronary thrombosis HSDN C0013421 Dystonia C0006309 Brucellosis HSDN C2315100 Pediatric failure to thrive C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C0003811 Cardiac rhythm disturbance C0597124 Obstructive asymmetric septal hypertrophy HPO C0233514 Behavior abnormal C0431399 Familial aplasia of the vermis MalaCards C1279888 Proteinuria of undiagnosed cause C0405580 Adrenal cortical hypofunction HSDN C1963093 Dizziness adverse event C0027858 Neuroma HSDN C0008031 Pain chest C1261473 Sarcoma HSDN C0003862 Pain joint C1264008 Chronic cold agglutinin disease MalaCards C2984058 Have pain C0041974 Urethral stricture HSDN C0011991 Loose stools C0027708 Nephroblastoma HSDN C0750937 Appendicular ataxia C2931903 Menzel type olivopontocerebellar atrophy MalaCards C1519353 Skin eruption papular C0346010 Multiple fibrofolliculomas OrphaNet|HPO|MalaCards C0030552 Paralysis partial C1963064 Anxiety adverse event HSDN C4042891 Sleep wake disorders C0010340 Critical illness HSDN C2237041 Shox gene with short stature C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency OrphaNet|HPO C4082202 Sleep quality question C0751254 Creutzfeldt-jakob disease, familial MalaCards C0027497 Queasy C0004238 Atrial fibrillation HSDN C0038990 Sweats C1956391 Temporal arteritis MalaCards|HPO C0851578 Disorder sleep C0022658 Kidney diseases HSDN C0015938 Fetal macrosomia C0020433 Hyperbilirubinemia HSDN C0020455 Hypergammaglobulinemia C0024143 Lupus nephritis HSDN C3641756 Have diarrhea C0024591 Malignant hyperpyrexia due to anesthesia HSDN C0024032 Birth weight subnormal C1291329 Transaldolase deficiency MalaCards|HPO C2984058 Have pain C1306577 Dies patient HSDN C0344428 Ventricular tachycardia by ecg finding C0340493 Paroxysmal familial ventricular fibrillation MalaCards C4084724 Usual severity constipation C0034067 Pulmonary emphysema HSDN C1963252 Tremor adverse event C0268274 Gangliosidoses, gm2 HSDN C0030193 Sense of pain C0007125 Carcinoma, ehrlich tumor HSDN C0004604 Pain back C0205769 Myxopapillary ependymoma UMLS C4085862 Bothered by nausea C0024305 Lymphoma, non-hodgkin HSDN C1963065 Apnea adverse event C1318518 Infantile malignant osteopetrosis MalaCards|HPO C4084775 Usual severity weight loss C0041234 Chagas disease HSDN C4084784 Diarrhea C0403447 Chronic kidney insufficiency HSDN C0042798 Vision dim C0014859 Esophageal neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041326 Pleural tuberculosis HSDN C0018772 Deafness C0035801 Diseases rodent HSDN C4084802 Usual severity diarrhea C0574960 Sacroiliitis HSDN C0030552 Paralysis partial C0008628 Chromosome deletion HSDN C1000483 Genus anemia C0346104 Follicular atrophoderma and basal cell epitheliomata OrphaNet|MalaCards C2984058 Have pain C0042063 Urogenital abnormalities HSDN C0038990 Sweats C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C0151786 Weakness muscle C0854912 Pineal germinoma HSDN C4084725 Usual severity cough C0002989 Epithelioid hemangioma of skin HSDN C4085317 Diarrhea frequency C3665596 Warts HSDN C2073625 X-ray of chest: pleural effusion C0026764 Multiple myeloma HPO C3463815 Feel fatigue C0006325 Bruxism HSDN C0002622 Amnesias C0032962 Pregnancy complications HSDN C1557397 Adverse event associated with pain C0027627 Neoplasm metastasis HSDN C0032617 High urine output C3151209 Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome HPO|UMLS C0406146 Meningococcal rash C0745283 Infectious process UMLS C0030193 Sense of pain C0017185 Gastrointestinal neoplasms HSDN C0151686 Growth retardation C2749559 Methemoglobinemia, type i HPO C3274924 Have been coughing C0002736 Amyotrophic lateral sclerosis HSDN C4084726 Distress cough C1962963 Osteoporosis adverse event HSDN C0015672 Decreased energy C0036983 Septic shock HSDN C0011168 Disorder deglutition C0019202 Hepatolenticular degeneration MalaCards|HPO C2984058 Have pain C0236792 Asperger syndrome HSDN C0007758 Cerebellar ataxia C0018801 Heart failure HSDN C0028081 Night sweat C0855080 Mixed cellularity hodgkin's disease stage i UMLS C0004134 Dyssynergia C0220754 Biotinidase deficiency OrphaNet|HSDN|UMLS|HPO|MalaCards C0151908 Dry skin C0022716 Menkes kinky hair syndrome OrphaNet|HPO|MalaCards C0413252 Hypothermia due to exposure C0016510 Foot diseases HSDN C1557397 Adverse event associated with pain C1739395 Takotsubo cardiomyopathy HSDN C1963252 Tremor adverse event C0019841 Classical swine fever HSDN C0030486 Extremity paralysis, lower C2937421 Prostatic hyperplasia HSDN C1557397 Adverse event associated with pain C0027664 Neoplasms, muscle tissue HSDN C0042940 Disorder of voice C0022661 Kidney failure, chronic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023760 Lip diseases HSDN C0427055 Face weakness C2675875 Chromosome 2p16.1 p15 deletion syndrome MalaCards C4085210 Usual severity pain C0013589 Ectromelia HSDN C0004134 Dyssynergia C0282577 Congenital disorders of glycosylation MalaCards|HSDN C4084768 Usual severity vomiting C4085635 Appetite quality question HSDN C0007398 Catatonic C0021819 Psychological interview HSDN C4084767 Bothered by vomiting C0027092 Myopia HSDN C0012833 Dizzy C0042510 Ventricular fibrillation HSDN C0009460 Communication impairment C0024919 Behavior, maternal HSDN C0020649 Blood pressure decreased C4054549 Medullary cystic kidney disease type i MalaCards C0020450 Hyperemesis gravidarum C0014544 Epilepsy HSDN C0030193 Sense of pain C1314678 Ameloblastic; carcinoma UMLS C0011991 Loose stools C0005891 Bodies image HSDN C1963066 Joint pain adverse event C0026760 Multiple epiphyseal dysplasia DiseaseOntology|MalaCards C4084773 Bothered by weight gain C0007193 Cardiomyopathy, dilated HSDN C0003811 Cardiac rhythm disturbance C0406645 Amyopathic dermatomyositis MalaCards C0019825 Voice hoarseness C1708650 Laryngeal basaloid carcinoma UMLS C0004604 Pain back C0038941 Incisional infection HSDN C0030486 Extremity paralysis, lower C1762616 Meningioma, benign, no icd-o subtype HSDN C0085636 Light sensitivity C0010035 Hereditary corneal dystrophy HSDN C0036572 Convulsion C0422852 Seizure, auditory, partial UMLS C0151889 Reflexes tendon increased C1838192 Spastic paraplegia 6, autosomal dominant (disorder) MalaCards C1961131 Cough adverse event C0007682 Cns disorder HSDN C2984057 Have nausea C0017658 Glomerulonephritis HSDN C1962957 Flushing adverse event C0017531 Angiolymphoid hyperplasia HSDN C0037763 Spasm C0042075 Urologic diseases HSDN C0004604 Pain back C0026850 Muscular dystrophy HSDN C4084802 Usual severity diarrhea C0162539 Igg deficiency HSDN C4084727 Cough frequency C0018200 Granuloma, respiratory tract HSDN C0518090 Frequency of pain question C0020598 Hypocalcemia HSDN C0424755 Fever symptoms C0014347 Enterobacteriaceae infections HSDN C0027497 Queasy C0038362 Stomatitis HSDN C0041834 Erythematous condition C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C3539896 Pelvic pain occurs with urination C0001261 Actinomycosis HSDN C0031315 Phantom limb pain C0042830 Perception visual HSDN C0018772 Deafness C0220704 Shprintzen syndrome OrphaNet C3641756 Have diarrhea C0002063 Alkalosis HSDN C0085593 Chill C0796561 Melanoma vaccines HSDN C4084774 Have weight loss C0029927 Ovarian cysts HSDN C0010200 Cough symptom C0854983 Lung adenocarcinoma, recurrent UMLS C0518090 Frequency of pain question C0024895 Bovine mastitis HSDN C0014591 Bleeding nose C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0010520 Skin cyanosis C0014116 Endocardial cushion defects HPO C0349489 Fetal hypoxia C0036690 Septicemia HSDN C2984057 Have nausea C0152054 Therapeutic touch HSDN C2203646 Jaundice C0037354 Smallpox HSDN C4084784 Diarrhea C0027662 Multiple endocrine neoplasia HSDN C0231218 Malaise generalized C2984092 Hepatocellular carcinoma by ajcc v7 stage UMLS C2096293 Ent surgical result ear vertigo C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C4084775 Usual severity weight loss C0037116 Silicosis HSDN C3665346 Loss sight C1854065 Late-onset retinal degeneration (disorder) HPO C0241210 Speaking delay C1859566 Bardet-biedl syndrome 8 HPO C4084776 Weight loss C0032708 Disorders of porphyrin metabolism HSDN C0013362 Dysarthrias C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0406216 Juvenile spring eruption C0021368 Inflammation UMLS C4085211 Pain distress question C0038017 Congenital spondylolisthesis HSDN C0038002 Spleen enlargement C1857395 De toni-debre-fanconi syndrome HPO C0004134 Dyssynergia C0271714 Hypoglycemia, leucine-induced HPO C0020673 Hypothermia (central) (local) C0035220 Respiratory distress syndrome, newborn HSDN C0030975 Disorders perception C0032962 Pregnancy complications HSDN C1963071 Back pain adverse event C0853697 Neutrophil count decreased HSDN C0015732 Feces incontinence C0431406 Asymmetric crying face association HPO C3687298 Choanal mass C3687297 Choanal mass due to trichomonas infection UMLS C0042963 Symptoms vomiting C3273127 Extrahepatic bile duct adenocarcinoma, gastric foveolar type UMLS C0423742 Intercourse pain C3160917 Bladder pain syndrome OrphaNet|MalaCards C4084768 Usual severity vomiting C0036982 Shock, hemorrhagic HSDN C0027497 Queasy C1258215 Ileus HSDN C4084726 Distress cough C0314657 Genetic predisposition HSDN C1963071 Back pain adverse event C0007193 Cardiomyopathy, dilated HSDN C3887784 Decreased urine output C0032914 Pre-eclampsia HSDN C0027498 Nausea vomiting C0600176 Argentaffinoma MalaCards C0030552 Paralysis partial C0008775 Ciguatera poisoning HSDN C0030552 Paralysis partial C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C0013421 Dystonia C0035242 Respiratory tract diseases HSDN C0018524 Hallucinate C1527429 Increased blood npn HSDN C0003550 Broca aphasia C0043251 Wounds and injuries HSDN C4084802 Usual severity diarrhea C0699744 Infection of ear HSDN C0233514 Behavior abnormal C0043207 Wolfram syndrome MalaCards|HPO C3898969 Have been vomiting C0040559 Toxoplasmosis in animals HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003618 Appetites HSDN C0024031 Back pain lower back C0035126 Reperfusion injury HSDN C3274924 Have been coughing C0007621 Neoplastic cell transformation HSDN C2017237 Left leg soft tissue swelling with black and blue discoloration C0151907 Discoloration of skin UMLS C0036659 Sensation disorder C3244301 Coverage level - family HSDN C0242670 Chronic vegetative state C0344315 Depressed mood HSDN C0033774 Skin pruritus C0042995 Vulvar neoplasms HSDN C0018784 Deafness sensorineural C1423541 Vangl2 gene HSDN C0010200 Cough symptom C0524799 Hyperlucent lung HSDN C0007758 Cerebellar ataxia C0025281 Meniere disease HSDN C0023014 Developmental disorder language C0014547 Epilepsies, partial HSDN C2024893 Cardiovascular surgery result: fatigue C0887833 Carcinoma, pancreatic ductal HSDN C0011991 Loose stools C0026640 Mouth neoplasms HSDN C4084768 Usual severity vomiting C0717360 Disease lyme vaccine HSDN C4084727 Cough frequency C1962963 Osteoporosis adverse event HSDN C4085211 Pain distress question C0020598 Hypocalcemia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0038454 Cerebrovascular accident HSDN C2984058 Have pain C0042266 Vaginismus HSDN C1963087 Constipation adverse event C0008625 Chromosome aberrations HSDN C3898969 Have been vomiting C0018567 Hand dermatoses HSDN C0150055 Pain chronic C0024141 Lupus erythematosus, systemic HSDN C3898969 Have been vomiting C0019066 Nontraumatic hemoperitoneum HSDN C0034933 Abnormal reflexes C0018799 Heart diseases HSDN C0019079 Bloody sputum C0032273 Pneumoconiosis HSDN C0557874 Global developmental delay C1841696 Macdermot patton williams syndrome MalaCards C0009676 Confusion state C0018839 Heat exhaustion HSDN C0011168 Disorder deglutition C2676770 Birk-barel mental retardation dysmorphism syndrome MalaCards|HPO C0009421 Comatose C0243010 Viral encephalitis HSDN C2237041 Shox gene with short stature C3151443 Dyskeratosis congenita, autosomal dominant 2 MalaCards C0747251 Paraparesis spastic progressive C1527231 Adrenomyeloneuropathy MalaCards C1384666 Decreased hearing C3463824 Myelodysplastic syndrome HSDN C0012833 Dizzy C0030920 Peptic ulcer HSDN|UMLS C0151908 Dry skin C0029294 Orofaciodigital syndromes MalaCards C0000727 Abdomen acute C1963067 Atrial fibrillation adverse event HSDN C0003862 Pain joint C0001624 Adrenal gland neoplasms HSDN C0033774 Skin pruritus C0025268 Multiple endocrine neoplasia type 2a HSDN C0033774 Skin pruritus C0748397 Reynolds syndrome OrphaNet|UMLS|HPO|MalaCards C0033377 Caudal displacement C2931051 Camptodactyly, joint contractures, facial skeletal defects OrphaNet|MalaCards C1406997 Thickening; tongue C0023795 Lipoid proteinosis of urbach and wiethe UMLS C3641756 Have diarrhea C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C0015230 Exanthem C0263398 Erythema elevatum diutinum OrphaNet|UMLS|MalaCards C0017181 Gastrointestinal bleed C1136033 Cutaneous mastocytosis MalaCards C0027066 Myoclonic jerking C0011849 Diabetes mellitus HSDN C0020580 Decreased sensation C3809738 Alacrima, achalasia, and mental retardation syndrome MalaCards C0009806 Constipate C0206245 Amyloid neuropathies, familial MalaCards|HSDN C0035078 Failure kidney C0032533 Polymyalgia rheumatica MalaCards C0011168 Disorder deglutition C0796028 Ataxia, fatal x-linked, with deafness and loss of vision MalaCards|HPO C4084774 Have weight loss C0020502 Hyperparathyroidism HSDN C0518090 Frequency of pain question C0019021 Hemoglobin c disease HSDN C3641755 Have constipation C0035372 Rett syndrome MalaCards|HSDN|HPO C0007859 Pain neck C0019829 Hodgkin disease HSDN C0557874 Global developmental delay C1848650 Ulnar hypoplasia with mental retardation MalaCards C4084775 Usual severity weight loss C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C0010200 Cough symptom C0024232 Lymphatic metastasis HSDN C0020580 Decreased sensation C0023518 Leukocytosis HSDN C1963093 Dizziness adverse event C0002736 Amyotrophic lateral sclerosis HSDN C0018808 Murmur C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4085211 Pain distress question C0037774 Spatial behavior HSDN C4084768 Usual severity vomiting C0079774 Peripheral t-cell lymphoma HSDN C4084802 Usual severity diarrhea C0025063 Mediastinal neoplasms HSDN C0033774 Skin pruritus C0014804 Erythromelalgia OrphaNet|HPO|MalaCards C0022346 Yellow skin C0041316 Lymph node tuberculosis HSDN C0005779 Clotting C2677590 Congenital disorder of glycosylation, type in OrphaNet|HPO|MalaCards C1260880 Nasal drip C2982437 Stage ii nasopharyngeal carcinoma UMLS C4085661 Usual severity nausea C0000771 Abnormalities, drug induced HSDN C0036572 Convulsion C1848199 X-linked lissencephaly OrphaNet|HPO|UMLS C4085317 Diarrhea frequency C2931542 Shapiro syndrome MalaCards C0042755 Virilisation C0023652 Lichen sclerosus et atrophicus HSDN C0013604 Edematous C0399424 Periapical abscess no sinus HSDN C4085222 Nausea C0032371 Poliomyelitis HSDN C0036572 Convulsion C0085315 Toxoplasmosis, cerebral HSDN C1963180 Neck pain adverse event C1548578 Location characteristic id - smoking HSDN C0010200 Cough symptom C0024899 Mastocytosis MalaCards C0263534 Beau's line C0333606 Dystrophies UMLS C1963093 Dizziness adverse event C1579931 Depressed - symptom HSDN C0015672 Decreased energy C0038644 Sudden infant death syndrome HSDN C0007859 Pain neck C0700327 Clinical findings relating to memory HSDN C0242936 Center pain C0035228 Respiratory hypersensitivity HSDN C2919142 Short stature adverse event C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C0036572 Convulsion C2931142 Dysharmonic skeletal maturation muscular fibre disproportion MalaCards C0024031 Back pain lower back C0024141 Lupus erythematosus, systemic HSDN C0023015 Language handicap C0035923 German measles vaccine HSDN C4084776 Weight loss C0019348 Herpes simplex infections HSDN C0023012 Delay language C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C0034150 Skin purpura C3266101 22q11 partial monosomy syndrome HPO C0043094 Weight gain C0035459 Atrophic rhinitis HSDN C0000727 Abdomen acute C0030299 Pancreatic pseudocyst HSDN C0042963 Symptoms vomiting C1269683 Major depressive disorder HSDN C4085661 Usual severity nausea C0001173 Adult pyloric stenosis HSDN C4084788 Have dizziness C0021400 Influenza HSDN C0424755 Fever symptoms C0085129 Bronchial hyperreactivity HSDN C4084775 Usual severity weight loss C0027055 Myocardial reperfusion injury HSDN C1279888 Proteinuria of undiagnosed cause C0016053 Fibromyalgia HSDN C0522224 Palsied C0008325 Cholecystitis HSDN C4084776 Weight loss C0018188 Granuloma HSDN C0015672 Decreased energy C0268314 Cholestasis-edema syndrome, norwegian type OrphaNet|MalaCards C0033377 Caudal displacement C0085920 Brachial neuralgia MalaCards C2911645 Weight loss adverse event C0001430 Adenoma HSDN C0013428 Painful urination C0036917 Sexually transmitted diseases, bacterial HSDN C1963137 Hydrocephalus adverse event C1956097 Wolf-hirschhorn syndrome MalaCards|HPO C4084726 Distress cough C0005659 Bite sting HSDN C0009676 Confusion state C0162671 Melas syndrome HSDN C0003079 Pupillary inequality C0025286 Meningioma HSDN C4084776 Weight loss C0023885 Liver abscess HSDN C4084726 Distress cough C0085092 Parenting behavior HSDN C0019572 Hairiness C0018564 Hand deformities HSDN C0015300 Ocular proptosis C1863389 Apert-crouzon disease MalaCards C0009792 Consciousness disorder C0085682 Hypophosphatemia HSDN C1963252 Tremor adverse event C0037315 Sleep apnea syndromes HSDN C4084724 Usual severity constipation C1552262 Nurse practitioner - family HSDN C4084768 Usual severity vomiting C0005779 Blood coagulation disorders HSDN C0027066 Myoclonic jerking C2984299 Asthma pathway HSDN C0031911 Pigment deposition C0031118 Peripheral nervous system neoplasms MalaCards C3641756 Have diarrhea C0854795 Resectable hepatic malignant neoplasm MalaCards C0002962 Angina C0023176 Lead poisoning HSDN C0022107 Fussiness C0221036 Acrodermatitis enteropathica HPO C0036572 Convulsion C1865117 Skeletal dysplasia and progressive central nervous system degeneration, lethal UMLS C0242936 Center pain C0025427 Mercury poisoning HSDN C4084767 Bothered by vomiting C0002949 Aneurysm, dissecting HSDN C0424755 Fever symptoms C0717360 Disease lyme vaccine HSDN C0557874 Global developmental delay C0406612 Encephalocraniocutaneous lipomatosis OrphaNet|HPO|MalaCards C0231712 Gait waddling C0270969 Zebra body myopathy OrphaNet|HPO|MalaCards C0020578 Hyperventilate C0011175 Dehydration HSDN C1069915 Vertigo C0007781 Intracranial embolism and thrombosis HSDN C1557397 Adverse event associated with pain C0162834 Hyperpigmentation HSDN C0162298 Stiffness joints C0795864 Smith-magenis syndrome MalaCards|HPO C0027066 Myoclonic jerking C1552262 Nurse practitioner - family HSDN C0026838 Spasticity muscle C2240378 Cleft palate on exam HSDN C2024893 Cardiovascular surgery result: fatigue C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C1963071 Back pain adverse event C0038395 Streptococcal infections HSDN C0034124 Pupillary disorder C0032001 Pituitary apoplexy HSDN C0518090 Frequency of pain question C3203360 Suppuration HSDN C1527344 Dysphonia C1855606 Burton syndrome MalaCards C0037316 Not enough sleeping C0314657 Genetic predisposition HSDN C0033377 Caudal displacement C0026691 Mucocutaneous lymph node syndrome MalaCards C4085211 Pain distress question C0021933 Intussusception HSDN C0851578 Disorder sleep C0040715 Chromosomal translocation HSDN C0000727 Abdomen acute C0235833 Congenital diaphragmatic hernia HSDN C0349489 Fetal hypoxia C0015923 Fetal alcohol syndrome HSDN C0009421 Comatose C0021051 Immunologic deficiency syndromes HSDN C0518090 Frequency of pain question C0003868 Arthritis, gouty HSDN C0036572 Convulsion C1837355 Leukodystrophy, hypomyelinating, 2 MalaCards|HPO|UMLS C0151786 Weakness muscle C0031036 Polyarteritis nodosa HSDN C0026821 Cramp C0039978 Thoracic diseases HSDN C0018681 Headache, cephalalgia C1299262 Sarcoma - category (morphologic abnormality) HSDN C3539893 Pelvic pain occurs with intercourse C0007621 Neoplastic cell transformation HSDN C3898969 Have been vomiting C0022116 Ischemia HSDN C0242936 Center pain C0085605 Liver failure HSDN C1963170 Hypothermia adverse event C0007570 Celiac disease HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027746 Nerve degeneration HSDN C4084802 Usual severity diarrhea C0010678 Cysticercosis HSDN C0007758 Cerebellar ataxia C1968551 Mental retardation, x-linked 79 MalaCards|HPO C4084766 Vomiting C0085298 Sudden cardiac death HSDN C4084723 Constipation C0002395 Alzheimer's disease HSDN C4085661 Usual severity nausea C0403447 Chronic kidney insufficiency HSDN C0242936 Center pain C0005639 Bisexual behavior HSDN C0151786 Weakness muscle C0004442 Avoidance learning HSDN C4084767 Bothered by vomiting C0040558 Toxoplasmosis HSDN C3274924 Have been coughing C0018798 Congenital heart defects HSDN C0018991 Paralysis one side of body C0004275 Attitude health HSDN C1963091 Diarrhea adverse event C0428478 Serum triglycerides raised HSDN C0003962 Ascites C0019156 Hepatic veno-occlusive disease OrphaNet|MalaCards C0007758 Cerebellar ataxia C0086647 Mucopolysaccharidosis type iiia MalaCards C0857305 Thrombocytopenia purpura C0041321 Tuberculosis, miliary HSDN C0022568 Inflammation corneal C1274795 Urban schosser spohn syndrome MalaCards C4084784 Diarrhea C0017601 Glaucomas HSDN C0012833 Dizzy C0152054 Therapeutic touch HSDN C0241165 Skin thickening C2931242 Familial waldmann's disease MalaCards C2984058 Have pain C0033677 Protein-energy malnutrition HSDN C0020580 Decreased sensation C0028850 Ocular motility disorders HSDN C0027796 Neuralgias C0051981 Anti-leprosy vaccine HSDN C1963252 Tremor adverse event C1704421 Skin pigmentation disorder HSDN C2203646 Jaundice C0042216 Poxvirus officinalis HSDN C0013421 Dystonia C3714514 Infection HSDN C0518090 Frequency of pain question C0027822 Neurodermatitis HSDN C0391860 Diffuse inflammations C3536864 Acute disseminated encephalitis UMLS C0030552 Paralysis partial C0003507 Aortic valve stenosis HSDN C4084774 Have weight loss C0000786 Spontaneous abortion HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040583 Tracheal stenosis HSDN C2024893 Cardiovascular surgery result: fatigue C0015461 Facial neoplasms HSDN C1263846 Attention deficit disorder with hyperactivity C0041341 Tuberous sclerosis HPO C1963137 Hydrocephalus adverse event C0751674 Lymphangioleiomyomatosis MalaCards|HPO C0009421 Comatose C0342727 3-@methylglutaconic aciduria, type i MalaCards|HPO C4084766 Vomiting C0751908 Vestibular neuronitis HSDN C0004134 Dyssynergia C0243010 Viral encephalitis HSDN C4084767 Bothered by vomiting C0155866 Inhalational anthrax OrphaNet|MalaCards C0018784 Deafness sensorineural C0032339 Rothmund-thomson syndrome MalaCards C0036572 Convulsion C0025289 Meningitis UMLS C0030552 Paralysis partial C3250443 Myotonic dystrophy 1 MalaCards C4084802 Usual severity diarrhea C0032966 Complication, neoplastic pregnancy HSDN C4084766 Vomiting C1690964 Cataract HSDN C0013378 Dysgensia C0038994 Gustatory sweating HSDN C4050613 Anxiety C0001231 Acth syndrome, ectopic MalaCards C0026826 High muscle tone C2940786 Thyroid hormone resistance syndrome HSDN C0040822 D tremors C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C0002962 Angina C0016542 Foreign body HSDN C0015230 Exanthem C0006845 Candidiasis, chronic mucocutaneous OrphaNet|HPO|MalaCards C0277959 Hair coarseness C1857068 Ectodermal dysplasia and neurosensory deafness OrphaNet|MalaCards C0023380 Lethargy C0242952 Behavior infants HSDN C4042891 Sleep wake disorders C0035228 Respiratory hypersensitivity HSDN C0150055 Pain chronic C3662064 Chronic nonmalignant pain UMLS C3463815 Feel fatigue C0007194 Hypertrophic cardiomyopathy HSDN C0751837 Gait ataxic C1839566 Charcot-marie-tooth disease, x-linked recessive, 5 UMLS C0423713 Ilioinguinal nerve neuralgia C1290865 Abdominal wall disorder UMLS C0022346 Yellow skin C1837218 Cleft palate, isolated HSDN C1963281 Vomiting adverse event C1855116 Methylmalonic aciduria, mut(-) type HPO C4084774 Have weight loss C0032285 Pneumonia HSDN C0242936 Center pain C0027429 Nasal obstruction present finding HSDN C1549543 Administration method - pain C0041955 Ureteral neoplasms HSDN C0011991 Loose stools C1837028 Severe combined immunodeficiency, autosomal recessive, t cell negative, b cell positive, nk cell positive HPO|UMLS C0030193 Sense of pain C0026277 Mixed salivary gland tumor HSDN C0034150 Skin purpura C2240374 Eosinophil count raised HSDN C3274924 Have been coughing C0024214 Lymphangiectasis HSDN C0011991 Loose stools C0009450 Disease caused by microorganism UMLS C0020538 Hbp C1412749 Bbs4 gene HPO C0586407 Cutaneous symptom C0031256 Petechiae UMLS C1549543 Administration method - pain C0740392 Infarction, middle cerebral artery HSDN C0030193 Sense of pain C0027707 Nephritis, interstitial HSDN C0010200 Cough symptom C0021368 Inflammation HSDN C0020505 Excessive eating C1857844 Williams-beuren region duplication syndrome MalaCards C0010520 Skin cyanosis C0032962 Pregnancy complications HSDN C0015469 Facial paralysis C0027962 Melanocytic nevus HSDN C1549543 Administration method - pain C0014547 Epilepsies, partial HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014474 Ependymoma HSDN C4084724 Usual severity constipation C0749420 Thyroid agenesis HPO C3665386 Abnormal vision C0877075 Intraosseous angioma MalaCards C3641755 Have constipation C0006057 Botulisms OrphaNet|MalaCards C2984058 Have pain C0043541 Zygomycoses HSDN C0018772 Deafness C1456781 Benign melanocytic nevus HSDN C0009421 Comatose C0027819 Neuroblastoma HSDN C1963087 Constipation adverse event C1961100 Erectile dysfunction adverse event HSDN C0035229 Respiratory function impaired C0024419 Waldenstrom macroglobulinemia OrphaNet|HPO|MalaCards C0015672 Decreased energy C0019326 Ventral hernia HSDN C0013604 Edematous C0021841 Intestinal neoplasms HSDN C1963086 Confusion adverse event C0007820 Cerebrovascular disorders HSDN C0020455 Hypergammaglobulinemia C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards|HPO C0312414 Spotting C0740785 Female_repro problem UMLS C0020580 Decreased sensation C0003794 Arm injury HSDN C0030552 Paralysis partial C0010074 Coronary vessel anomalies HSDN C0009792 Consciousness disorder C0238265 Encephalopathy, callosal demyelinating HSDN C0022346 Yellow skin C0002726 Amyloidosis HSDN C0013604 Edematous C0027080 Myoglobinuria HSDN C3898969 Have been vomiting C0039981 Thoracic neoplasms HSDN C0002624 Amnesia retrograde C1449593 Cataleptic freezing reaction HSDN C0002170 Alopecia disorders C1333764 Gastric cronkhite canada polyposis MalaCards C0013604 Edematous C0023893 Liver cirrhosis, experimental HSDN C3463815 Feel fatigue C0034067 Pulmonary emphysema HSDN C0917816 Deficiency mental C3152055 D-2-hydroxyglutaric aciduria 1 HPO C0011991 Loose stools C0033375 Prolactinoma HSDN C0004941 Behavioral symptoms C0034494 Rabies (disorder) OrphaNet C2108112 Continuous electrocardiogram ventricular fibrillation C2678485 Long qt syndrome 9 (disorder) MalaCards C2984058 Have pain C0023885 Liver abscess HSDN C0518090 Frequency of pain question C0236964 Attention deficit and disruptive behavior disorders HSDN C0030193 Sense of pain C1706980 Bone leiomyoma UMLS C3665347 Vision impaired C1845069 Albinism, ocular, with late-onset sensorineural deafness (disorder) OrphaNet C1963184 Nystagmus adverse event C1839730 Prieto x-linked mental retardation syndrome MalaCards C0011206 Delirium acute C1000483 Genus anemia HSDN C4085317 Diarrhea frequency C2137063 Ent surgical result - speech HSDN C2919142 Short stature adverse event C0340951 Erythrogenesis imperfecta MalaCards C0042571 Vertigo subjective C1510412 Pseudoaneurysm HSDN C0018772 Deafness C0023646 Lichen planus HSDN C0013404 Respiratory difficulty C1691228 Cystic kidney diseases HSDN C2911645 Weight loss adverse event C0024636 Malocclusion HSDN C4084724 Usual severity constipation C0024668 Mammary neoplasms, experimental HSDN C0015672 Decreased energy C0003493 Aortic diseases HSDN C0003862 Pain joint C1836315 Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia MalaCards C0030193 Sense of pain C0027644 Neoplasm regression, spontaneous HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3714644 Thymus neoplasms HSDN C0011991 Loose stools C0043208 Wolman disease HPO C4084897 Sleep disturbance subordinate domain C0342443 Adrenal cushing's syndrome MalaCards C3815497 Cough C0017658 Glomerulonephritis HSDN C0018772 Deafness C1510455 Acrocephalosyndactylia MalaCards|HSDN C0018991 Paralysis one side of body C0011303 Demyelinating diseases HSDN C0022408 Disorder joint C0029411 Osteoarthropathy, primary hypertrophic HPO C1963184 Nystagmus adverse event C1837073 Spondylometaphyseal dysplasia with cone-rod dystrophy OrphaNet|HPO C0033774 Skin pruritus C0024901 Mastocytosis, diffuse cutaneous OrphaNet|MalaCards C4085222 Nausea C0021847 Intestinal pseudo-obstruction HSDN C4084802 Usual severity diarrhea C0025149 Medulloblastoma HSDN C0015672 Decreased energy C1332464 Basaloid carcinoma of thymus UMLS C0018524 Hallucinate C0026266 Mitral valve insufficiency HSDN C4042891 Sleep wake disorders C0024535 Malaria, falciparum HSDN C3541349 Syncope C0032787 Postoperative complications HSDN C0349588 Stature short C0086438 Hypogammaglobulinemia MalaCards C0015469 Facial paralysis C0238288 Muscular dystrophy, facioscapulohumeral MalaCards|HPO C0027497 Queasy C0004623 Bacterial infections HSDN C2242996 Tingling C0005967 Bone neoplasms HSDN C0151786 Weakness muscle C0001883 Airway obstruction HSDN C2984058 Have pain C0852795 Increased insulin level HSDN C2032483 Thigh pain radiates down leg subsides when walking stops C0006413 Burkitt lymphoma MalaCards C0013428 Painful urination C1519934 Vaginal undifferentiated carcinoma UMLS C0009792 Consciousness disorder C0007020 Carbon monoxide poisoning HSDN C0460137 Push down or depress C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO C0542476 Forgetful C1836148 Supranuclear palsy, progressive, 2 MalaCards|UMLS C0231528 Muscle pain generalized C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C1963252 Tremor adverse event C0011334 Dental caries HSDN C0042024 Urine incontinence C0023467 Leukemia, myelocytic, acute HSDN C0007758 Cerebellar ataxia C0026975 Myelitis HSDN C0008031 Pain chest C0162316 Iron deficiency anemia UMLS C4084774 Have weight loss C0036974 Shock HSDN C0242936 Center pain C0553980 Endomyocardial fibrosis HSDN C0851578 Disorder sleep C0018671 Head and neck neoplasms HSDN C1963249 Tinnitus adverse event C0022116 Ischemia HSDN C4084776 Weight loss C0752087 Myasthenia gravis, autoimmune, experimental HSDN C0005779 Clotting C0242584 Autoimmune thrombocytopenia MalaCards C0013404 Respiratory difficulty C1527311 Brain edema HSDN C1962956 Flatulence adverse event C0014547 Epilepsies, partial HSDN C0010200 Cough symptom C0039483 Giant cell arteritis MalaCards|HPO C1549543 Administration method - pain C0032087 Plant poisoning HSDN C4084726 Distress cough C0011311 Dengue fever HSDN C0424755 Fever symptoms C0024437 Macular degeneration HSDN C0413252 Hypothermia due to exposure C0022650 Kidney calculi HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0436596 On examination - apathetic HSDN C4084773 Bothered by weight gain C0220847 C hepatitis virus HSDN C1963071 Back pain adverse event C0022660 Kidney failure, acute HSDN C0518090 Frequency of pain question C0013884 Filarial elephantiases HSDN C0917816 Deficiency mental C1855794 Bamforth syndrome OrphaNet|HPO C0039070 Collapse fleeting C0039128 Syphilis HSDN C0018784 Deafness sensorineural C0264939 Systemic vasculitis HSDN C1557397 Adverse event associated with pain C0020651 Hypotension, orthostatic HSDN C1961131 Cough adverse event C0025063 Mediastinal neoplasms HSDN C1384666 Decreased hearing C3888337 Deafness, autosomal recessive 96 MalaCards C4085317 Diarrhea frequency C3495559 Juvenile arthritis HSDN C0518090 Frequency of pain question C0029423 Cartilaginous exostosis HSDN C4084776 Weight loss C1706377 Memory device component HSDN C0018834 Brash C1263858 Muscular dystrophy congenital, merosin negative OrphaNet|HPO C0030193 Sense of pain C0042018 Urinary calculi HSDN C0016199 Pain flank C0022681 Medullary sponge kidney HSDN C0011570 Monopolar depression C0002986 Fabry disease MalaCards|HPO C2364082 Hyposmia C1328931 Multiple lentigines MalaCards C4084766 Vomiting C0011603 Dermatitis HSDN C3665346 Loss sight C0019562 Von hippel-lindau syndrome MalaCards|HPO C4085211 Pain distress question C0017128 Fistula gastric HSDN C0042571 Vertigo subjective C0024535 Malaria, falciparum HSDN C0162834 Hyperpigmentation C3468041 Fanconi anemia, complementation group c MalaCards C0030200 Intractable pain C1999266 Depression adverse event HSDN C0518090 Frequency of pain question C0008373 Cholesteatoma HSDN C0022346 Yellow skin C0023794 Lipoidosis HSDN C1557397 Adverse event associated with pain C0033680 Protein-losing enteropathies HSDN C3829611 Nausea frequency C0032851 Disease poultry HSDN C0497406 Over weight C0151526 Premature birth HSDN C4085210 Usual severity pain C0043325 Xanthomatosis HSDN C3641755 Have constipation C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C3815497 Cough C0282607 Vascular neoplasms HSDN C3641755 Have constipation C0027746 Nerve degeneration HSDN C0018681 Headache, cephalalgia C0002940 Aneurysm UMLS C0008031 Pain chest C0009241 Cognition disorders HSDN C1860844 Sparse, thin hair C1843042 Craniolenticulosutural dysplasia OrphaNet|HPO|MalaCards C0221232 Welts C1304195 Autoimmune angio-oedema UMLS C0018772 Deafness C0017416 Genital neoplasms, female HSDN C0239376 Lower extremity pain C0740728 Lower extremity problem UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0043119 Werner syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0037268 Skin abnormalities HSDN C0002962 Angina C0038661 Suicide HSDN C0030975 Disorders perception C0302148 Blood clot HSDN C2911645 Weight loss adverse event C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C3887873 Hearing loss C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0043094 Weight gain C0004763 Barrett esophagus HSDN C0518090 Frequency of pain question C0007871 Uterine cervical incompetence HSDN C3463815 Feel fatigue C0023240 Legionellosis OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C0268237 Cytochrome-c oxidase deficiency MalaCards|HPO C0023380 Lethargy C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO|UMLS C4084775 Usual severity weight loss C0007121 Bronchogenic carcinoma HSDN C4085211 Pain distress question C0161406 Injury nerve trigeminal HSDN C0041657 Consciousness loss C0032962 Pregnancy complications HSDN C1963184 Nystagmus adverse event C1412397 Ancr gene HPO C0241137 Skin pallor C0024537 Malaria, vivax HSDN C4050613 Anxiety C2931205 Usher syndrome, type 1a MalaCards C0009421 Comatose C2240378 Cleft palate on exam HSDN C0018772 Deafness C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C0494475 Seizure generalized tonic clonic C0917800 Epilepsy, myoclonic, infantile OrphaNet|MalaCards C1963281 Vomiting adverse event C1720922 Respiratory aspiration HSDN C4085210 Usual severity pain C0340629 Aortic aneurysm without mention of rupture nos HSDN C0018772 Deafness C0035335 Retinoblastoma HSDN C0010038 Corneal opacity disorder C2720163 Placental steroid sulfatase deficiency MalaCards C3641755 Have constipation C0018802 Congestive heart failure HSDN C0000737 Abdomen pain C0037579 Soft tissue neoplasms HSDN C0013604 Edematous C1306214 Acth-secreting pituitary adenoma HPO C3887873 Hearing loss C0020502 Hyperparathyroidism HSDN C2237041 Shox gene with short stature C3469605 Pseudohypoaldosteronism, type iid MalaCards C3641756 Have diarrhea C0015461 Facial neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0026764 Multiple myeloma OrphaNet|HSDN|HPO C0018772 Deafness C3888029 Deafness, autosomal dominant 54 MalaCards C4084784 Diarrhea C0025286 Meningioma HSDN C3887873 Hearing loss C0796202 Wittwer syndrome MalaCards C3539893 Pelvic pain occurs with intercourse C0033348 Language program HSDN C4085317 Diarrhea frequency C0149931 Migraine disorders HSDN C0015469 Facial paralysis C0022665 Kidney neoplasm HSDN C1549543 Administration method - pain C0018671 Head and neck neoplasms HSDN C1069915 Vertigo C2586211 Thrombosis of blood vessel HSDN C4085317 Diarrhea frequency C0011269 Dementia, vascular HSDN C0085631 Abnormal excitement C0038454 Cerebrovascular accident HSDN C0917816 Deficiency mental C2931366 Congenital deformity of the thumb and congenital alopecia MalaCards C0018834 Brash C3553517 Cornelia de lange syndrome 4 MalaCards C0018520 Breath odor C0016879 Fusobacterium infections HSDN C0344315 Mood depressed C0085209 Bovine spongiform encephalitis MalaCards C0024031 Back pain lower back C0026847 Spinal muscular atrophy HSDN C0009676 Confusion state C0013928 Fat embolism HSDN C3887873 Hearing loss C1853566 Genitopatellar syndrome MalaCards C0013395 Indigestion C0002792 Anaphylaxis HSDN C0270948 Neurogenic muscular atrophy C3809592 Mitochondrial dna depletion syndrome 13 (encephalomyopathic type) MalaCards C0037384 Snore C0005935 Bone conduction HSDN C0030193 Sense of pain C0079218 Fibromatosis, aggressive HSDN C0020538 Hbp C1969107 Corticosteroid-binding globulin, elevated HPO C4084784 Diarrhea C0268225 Aspartylglucosaminuria MalaCards|HPO C3641756 Have diarrhea C0020877 Ileitis DiseaseOntology|MalaCards C0018784 Deafness sensorineural C0022081 Iritis HSDN C2126130 Epistaxis from the right nostril C0014591 Epistaxis UMLS C1963091 Diarrhea adverse event C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C3494358 Characteristic, prodromal C4050517 Social skills HSDN C0036572 Convulsion C0012691 Dislocations HSDN C0018681 Headache, cephalalgia C1709884 Regional adrenal gland chromaffin neoplasm UMLS C0012569 Double vision C0020550 Hyperthyroidism HSDN C0020452 Engorgement C0037054 Sickle cell trait MalaCards C1557397 Adverse event associated with pain C0009187 Coccidiosis HSDN C0000737 Abdomen pain C1334809 Mucinous adenocarcinoma of stomach UMLS C0027796 Neuralgias C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2029884 Hearing loss by exam C0018916 Hemangioma HSDN C0010038 Corneal opacity disorder C2713321 Alpha-l-iduronidase deficiency OrphaNet C0012833 Dizzy C0011881 Diabetic nephropathy HSDN C0917816 Deficiency mental C1838625 Warburg sjo fledelius syndrome HPO C0221263 Cafe au lait spot C3149711 Pheochromocytoma, susceptibility to HPO C0041834 Erythematous condition C0796093 Odontoonychodermal dysplasia MalaCards|HPO C4085211 Pain distress question C0020119 Human development HSDN C4084768 Usual severity vomiting C0026266 Mitral valve insufficiency HSDN C0035078 Failure kidney C0221032 Familial generalized lipodystrophy MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C3151113 Meier-gorlin syndrome 3 MalaCards|HPO C0522224 Palsied C0040038 Thromboembolism HSDN C1963071 Back pain adverse event C0162820 Dermatitis, allergic contact HSDN C1279888 Proteinuria of undiagnosed cause C2911643 Encounter due to family history of osteoporosis HSDN C3898969 Have been vomiting C0344479 Spinal cord myelodysplasia HSDN C0019209 Large liver C0272051 Xerocytosis HPO C4084727 Cough frequency C1000483 Genus anemia HSDN C0018834 Brash C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C1961131 Cough adverse event C0032962 Pregnancy complications HSDN C0026838 Spasticity muscle C4225200 Combined oxidative phosphorylation deficiency 29 UMLS C0036572 Convulsion C0008370 Cholestasis HSDN C0233756 Complaint somatic multiple C0001175 Acquired immunodeficiency syndrome UMLS C1384666 Decreased hearing C1858562 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 MalaCards|HPO C1962972 Proteinuria adverse event C1963067 Atrial fibrillation adverse event HSDN C0026838 Spasticity muscle C0039082 Syndrome HSDN C0002622 Amnesias C0023702 Injury lightning HSDN C0270948 Neurogenic muscular atrophy C0265253 Stickler syndrome (disorder) MalaCards C0026205 Pupillary constriction C0026499 Monosomy HSDN C2700617 Irritation - emotion C0020074 Hsan type iv OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0003869 Arthritis, infectious HSDN C0039070 Collapse fleeting C0085417 Epilepsy, complex partial HSDN C3494358 Characteristic, prodromal C0035021 Relapsing fever HSDN C0009806 Constipate C0520681 Central alveolar hypoventilation syndrome MalaCards C0010038 Corneal opacity disorder C1961835 Gaucher disease, type 1 MalaCards C4085862 Bothered by nausea C0431109 Choroid plexus carcinoma HPO C0013404 Respiratory difficulty C0039685 Tetralogy of fallot HSDN C1963184 Nystagmus adverse event C0796028 Ataxia, fatal x-linked, with deafness and loss of vision MalaCards|HPO C0023014 Developmental disorder language C0036357 Psychology, schizophrenic HSDN C4084776 Weight loss C0029132 Disorder of the optic nerve HSDN C0476273 Distress respiratory C0027126 Myotonic dystrophy MalaCards|HPO C4084768 Usual severity vomiting C0268547 Argininosuccinic aciduria MalaCards|HPO C4085211 Pain distress question C0396023 Chronic adenoiditis DiseaseOntology|MalaCards C0206146 Myocardial stunning C0018790 Cardiac arrest HSDN C0012833 Dizzy C0020619 Hypogonadism HSDN C1963064 Anxiety adverse event C0339534 Usher syndrome type 2 MalaCards|HPO C2911645 Weight loss adverse event C0040411 Tongue neoplasms HSDN C1963091 Diarrhea adverse event C0041971 Tumor urethra HSDN C0011991 Loose stools C0036117 Salmonella infections UMLS C0522224 Palsied C0024003 Lordosis HSDN C3641756 Have diarrhea C0040128 Thyroid diseases HSDN C0423773 Skin scaly C3489725 Pseudo-torch syndrome MalaCards C3665347 Vision impaired C1856973 Encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration MalaCards C0015300 Ocular proptosis C3278138 Fibrochondrogenesis 1 MalaCards C0013595 Eczematous dermatitis C0265962 Ichthyosis linearis circumflexa OrphaNet|HPO|MalaCards C2203646 Jaundice C0016154 Fish disease HSDN C1963071 Back pain adverse event C0026769 Multiple sclerosis HSDN C0020673 Hypothermia (central) (local) C0030922 Peptic ulcer hemorrhage HSDN C4084723 Constipation C0032371 Poliomyelitis HSDN C0151686 Growth retardation C0265492 Anomaly of chromosome pair ring 22 syndrome MalaCards C0234132 Pyramidal sign C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0198632 Pneumoperitoneum HSDN C1000483 Genus anemia C0019911 Hookworm infections MalaCards C1549543 Administration method - pain C0085129 Bronchial hyperreactivity HSDN C1963091 Diarrhea adverse event C0019372 Herpesviridae infections HSDN C0030794 Pelvis pain C0010692 Cystitis HSDN C1963091 Diarrhea adverse event C2931876 Hirschsprung disease 1 MalaCards C0454644 Delayed language development C0796250 Partington x-linked mental retardation syndrome HPO C0000727 Abdomen acute C0041296 Tuberculosis HSDN C4085548 Usual severity dizziness C0403447 Chronic kidney insufficiency HSDN C0018681 Headache, cephalalgia C0027821 Syndrome effort HSDN C0518090 Frequency of pain question C0027831 Neurofibromatosis 1 HSDN C2911645 Weight loss adverse event C0033941 Psychoses, substance-induced HSDN C1557397 Adverse event associated with pain C0015461 Facial neoplasms HSDN C1963170 Hypothermia adverse event C1963083 Cholecystitis adverse event HSDN C0162298 Stiffness joints C0877750 Stiffness of joint, nec, involving hand in mdr19_0 UMLS C0413252 Hypothermia due to exposure C0021603 Sleep initiation and maintenance disorders HSDN C1963067 Atrial fibrillation adverse event C4015285 Cardiac conduction disease with or without dilated cardiomyopathy MalaCards C2237041 Shox gene with short stature C2750066 Spondylo-megaepiphyseal-metaphyseal dysplasia MalaCards C2024893 Cardiovascular surgery result: fatigue C0600519 Ventricular remodeling HSDN C0242936 Center pain C0011880 Diabetic ketoacidosis HSDN C0040822 D tremors C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO|UMLS C0030552 Paralysis partial C0025312 Meningomyelocele HSDN C0040822 D tremors C0033922 Psychomotor disorders MalaCards C0233514 Behavior abnormal C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0032584 Polyps HSDN C0036572 Convulsion C3281202 Mental retardation, autosomal dominant 13 MalaCards C0011991 Loose stools C1290398 Cerebral arterial aneurysm HSDN C0000737 Abdomen pain C2749759 Macrothrombocytopenia-stomatocytosis, mediterranean HPO C4085222 Nausea C0002991 Cutaneous fibrous histiocytoma HSDN C0237326 Defecation pain C0265246 Townes syndrome OrphaNet|HPO|MalaCards C0003862 Pain joint C0009782 Connective tissue diseases HSDN C0030486 Extremity paralysis, lower C0039980 Chest injury HSDN C0850758 Pain pelvic C0033575 Prostatic diseases HSDN C0027066 Myoclonic jerking C0007784 Cerebral hemisphere hemorrhage HSDN C0018681 Headache, cephalalgia C0043167 Pertussis HSDN C0231807 Dyspnea exertional C0003507 Aortic valve stenosis MalaCards C3463815 Feel fatigue C0872996 Q fever vaccine HSDN C0002962 Angina C0035229 Respiratory insufficiency HSDN C1971624 Appetite absent C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C0494475 Seizure generalized tonic clonic C0030779 Pelger-huet anomaly MalaCards|HPO C4085862 Bothered by nausea C0014836 Escherichia coli infections HSDN C0004134 Dyssynergia C3279839 Mental retardation, autosomal dominant 7 MalaCards C0011206 Delirium acute C0019080 Hemorrhage HSDN C0085128 Cardiac output elevated C0032045 Placenta disorders HSDN C4084784 Diarrhea C0020097 Htlv-i infections HSDN C0040485 Wryneck C0034929 Reflex HSDN C0003811 Cardiac rhythm disturbance C0587248 Costello syndrome (disorder) MalaCards|HPO C2911645 Weight loss adverse event C0000809 Abortion, habitual HSDN C0003862 Pain joint C0949690 Spondylarthritis HSDN C0030193 Sense of pain C0023786 Mucopolysaccharidosis i HSDN C0040822 D tremors C0007959 Charcot-marie-tooth disease HSDN C0557874 Global developmental delay C3809236 Muscular dystrophy, limb-girdle, type 2s MalaCards C0857305 Thrombocytopenia purpura C2239112 Blister dosing unit HSDN C3665347 Vision impaired C0268680 Biotin deficiency MalaCards C0017672 Pain tongue C1547046 Kind of quantity - taste HSDN C3829611 Nausea frequency C0152724 Tuberculosis of intestines and mesenteric glands DiseaseOntology|MalaCards C4084774 Have weight loss C0011630 Dermatomycoses HSDN C0042024 Urine incontinence C1269683 Major depressive disorder HSDN C0162298 Stiffness joints C0086647 Mucopolysaccharidosis type iiia MalaCards|HPO|UMLS C4085549 Dizziness C0018798 Congenital heart defects HSDN C1549543 Administration method - pain C1962974 Chylothorax adverse event HSDN C0018524 Hallucinate C0009651 Conditioning operant HSDN C2919142 Short stature adverse event C3808414 Perrault syndrome 3 MalaCards C0037383 Sneeze C0037050 Sick building syndrome HSDN C0948844 Lancinating pains C1842586 Neuropathy, hereditary sensory and autonomic, type i, with cough and gastroesophageal reflux UMLS C0020580 Decreased sensation C0027804 Fatigue neurosis HSDN C0030486 Extremity paralysis, lower C0006118 Brain neoplasms HSDN C0015672 Decreased energy C0017601 Glaucomas HSDN C0231218 Malaise generalized C2062404 Acute space motion sickness involving malaise UMLS C1557397 Adverse event associated with pain C0001122 Acidosis HSDN C0015469 Facial paralysis C0041374 Tumor virus infections HSDN C0042571 Vertigo subjective C0013295 Duodenal ulcer HSDN C4085210 Usual severity pain C0039614 Tetanus HSDN C0011168 Disorder deglutition C1527226 Crst syndrome MalaCards C0016382 Cutaneous vascular engorgement C0406756 Keratolytic winter erythema OrphaNet|MalaCards C0150045 Urinary incontinence urge C0020258 Hydrocephalus, normal pressure HSDN C2984058 Have pain C0206694 Mucoepidermoid carcinoma HSDN C0003862 Pain joint C0037005 Shoulder dislocation HSDN C1557397 Adverse event associated with pain C0019372 Herpesviridae infections HSDN C4085548 Usual severity dizziness C0032343 Poisoning HSDN C3541349 Syncope C3501836 Long qt syndrome 3-6 MalaCards C2203646 Jaundice C0032763 Post gastrectomy syndrome HSDN C2242996 Tingling C3888109 Acromelalgia hereditary MalaCards C3463815 Feel fatigue C0520946 Emotional hypersensitivity HSDN C0000737 Abdomen pain C2717906 Hereditary angioedema type i HPO|UMLS C0242670 Chronic vegetative state C0027902 Neuropsychological diagnosis HSDN C0917816 Deficiency mental C0268569 Intermittent maple syrup urine disease HPO C3887873 Hearing loss C0008441 Chondroblastoma HSDN C4084768 Usual severity vomiting C0037929 Spinal cord injuries HSDN C0022638 Ketosis C0574108 Glycerol kinase deficiency - isolated MalaCards C0020438 Hypercalciuria C0011351 Dental enamel hypoplasia HSDN C0013604 Edematous C0013806 Electroplexy shock therapy HSDN C2315100 Pediatric failure to thrive C0917990 Acro-osteolysis MalaCards C0018681 Headache, cephalalgia C0022650 Kidney calculi HSDN C4085222 Nausea C1145670 Respiratory failure HSDN C0151889 Reflexes tendon increased C3554195 Epileptic encephalopathy, early infantile, 14 MalaCards C4084767 Bothered by vomiting C0428977 Bradycardia HSDN C0025287 Meningitis-like C0030636 Pasteurella infection DiseaseOntology|MalaCards C0518090 Frequency of pain question C0037305 Neoplasm, skull HSDN C1963086 Confusion adverse event C1546847 Entity name part type - family HSDN C0023012 Delay language C3266843 47, xyy syndrome OrphaNet C0494475 Seizure generalized tonic clonic C0342273 Transient neonatal diabetes mellitus MalaCards C0020673 Hypothermia (central) (local) C1306759 Eosinophilic disorder HSDN C4042891 Sleep wake disorders C2827407 Infectious otitis media HSDN C0008031 Pain chest C0085096 Peripheral vascular diseases HSDN|UMLS C0042928 Paralysis vocal cord C0041296 Tuberculosis HSDN C0009676 Confusion state C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0270948 Neurogenic muscular atrophy C3150169 Frontotemporal lobar degeneration with tdp43 inclusions, tardbp-related HPO C0013362 Dysarthrias C1458155 Mammary neoplasms HSDN C2024878 Cardiovascular surgery result: dyspnea C0003490 Aortic arch syndrome HSDN C2830326 Unsteadiness on feet C0154725 Oth disorder nervous system UMLS C2911647 Weight gain adverse event C0004943 Behcet syndrome HSDN C0042025 Urinary incontinence stress C0024841 Matrimony, matrimonial HSDN C2237041 Shox gene with short stature C4014343 Mental retardation, autosomal recessive 42 MalaCards C0018784 Deafness sensorineural C0040411 Tongue neoplasms HSDN C2237041 Shox gene with short stature C0795949 Galloway mowat syndrome OrphaNet|HPO|MalaCards C0349588 Stature short C0043346 Xeroderma pigmentosum MalaCards|HPO C2911645 Weight loss adverse event C0035309 Retinal diseases HSDN C0036572 Convulsion C0043207 Wolfram syndrome OrphaNet|UMLS|HPO|MalaCards C0155552 Hearing loss mixed C1265748 Torsion HSDN C0557874 Global developmental delay C1853100 Cerebrooculofacioskeletal syndrome 4 MalaCards|HPO C4085641 Level of joint pain C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C0027796 Neuralgias C0042133 Uterine fibroids HSDN C0454644 Delayed language development C1860224 Ablepharon-macrostomia syndrome OrphaNet|HPO|MalaCards C0013378 Dysgensia C0019100 Severe dengue HSDN C1557397 Adverse event associated with pain C0020514 Hyperprolactinemia HSDN C0860603 Anxiety symptom C2675897 1q21.1 contiguous gene deletion MalaCards C0008031 Pain chest C0020443 Hypercholesterolemia HSDN|UMLS C0242936 Center pain C0030767 Grouping peer HSDN C0522224 Palsied C0029408 Degenerative polyarthritis HSDN C0020505 Excessive eating C0205734 Diabetes, autoimmune MalaCards C0013395 Indigestion C0162576 Anisakiasis HSDN C0018926 Emesis bloody C0037369 Smoking HSDN C3541349 Syncope C0036421 Systemic scleroderma HSDN C0018772 Deafness C0079731 B-cell lymphomas HSDN C1963281 Vomiting adverse event C0004626 Pneumonia, bacterial HSDN C0037763 Spasm C1881674 Medical device emits smoke HSDN C0026838 Spasticity muscle C2026474 Hemiplegic cerebral palsy with spasticity UMLS C0007758 Cerebellar ataxia C0011849 Diabetes mellitus HSDN C0018834 Brash C2748910 Rett syndrome, atypical OrphaNet|HPO|MalaCards C0026858 Musculoskeletal pain C0158322 Calcaneus spur HSDN C0151786 Weakness muscle C0007873 Uterine cervical neoplasm HSDN C4085549 Dizziness C0026650 Movement disorders HSDN C3641755 Have constipation C0271737 Addison's disease due to autoimmunity OrphaNet C0018524 Hallucinate C0018916 Hemangioma HSDN C4084784 Diarrhea C0282687 Hemorrhagic fever, ebola DiseaseOntology|OrphaNet|MalaCards C0012833 Dizzy C0027663 Neoplasms, multiple primary HSDN C0023380 Lethargy C0023518 Leukocytosis HSDN|UMLS C0027497 Queasy C0033873 Psychiatry HSDN C0019209 Large liver C0016952 Galactosemias OrphaNet|MalaCards C0036572 Convulsion C1829813 Malonic acidemia MalaCards C0038002 Spleen enlargement C2717750 Platelet alpha-granule deficiency MalaCards C0030200 Intractable pain C3827868 Tachycardia by ecg finding HSDN C0030193 Sense of pain C0024266 Lymphocytic choriomeningitis HSDN C0042384 Vasculitis, nonspecific C1328840 Autoimmune lymphoproliferative syndrome MalaCards|HPO C0085636 Light sensitivity C1836122 Sarcoidosis, early-onset MalaCards C0742283 Chest pain atypical prolonged C0027051 Myocardial infarction UMLS C0013404 Respiratory difficulty C0040558 Toxoplasmosis HSDN C3815497 Cough C0007621 Neoplastic cell transformation HSDN C0242936 Center pain C0014118 Endocarditis HSDN C0018834 Brash C0038454 Cerebrovascular accident HSDN C2911647 Weight gain adverse event C0005779 Blood coagulation disorders HSDN C0030552 Paralysis partial C0409988 Focal nodular myositis MalaCards C0151686 Growth retardation C1848030 Hypotonia-cystinuria syndrome OrphaNet|HPO|MalaCards C0032781 Postnasal drip C0810016 Other upper respiratory infections UMLS C4085642 Level of joint stiffness C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C2117329 X-ray of toe: polydactyly HSDN C0029163 Hemorrhage mouth C0040422 Tonsillar neoplasms HSDN C0032617 High urine output C0025517 Metabolic diseases HSDN|UMLS C4085862 Bothered by nausea C0042331 Migraine variant MalaCards C0234428 Consciousness disturbance C0003490 Aortic arch syndrome MalaCards C0039070 Collapse fleeting C3697638 Familial short qt syndrome MalaCards C0018681 Headache, cephalalgia C0037997 Splenic diseases HSDN C0151908 Dry skin C1835265 Lymphedema, microcephaly and chorioretinopathy syndrome MalaCards C4084725 Usual severity cough C0010054 Coronary arteriosclerosis HSDN C4084776 Weight loss C0037047 Sibling HSDN C0041657 Consciousness loss C0021568 Bites insect stings HSDN C0231218 Malaise generalized C2981634 Stage ii hilar cholangiocarcinoma UMLS C2203646 Jaundice C0019829 Hodgkin disease HSDN C0015672 Decreased energy C0032273 Pneumoconiosis HSDN C4042891 Sleep wake disorders C0030318 Panic state HSDN C0034933 Abnormal reflexes C0007781 Intracranial embolism and thrombosis HSDN C1557397 Adverse event associated with pain C1527336 Sjogren's syndrome HSDN C4085222 Nausea C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C1963252 Tremor adverse event C0007784 Cerebral hemisphere hemorrhage HSDN C4084723 Constipation C0206247 Amyloid neuropathies MalaCards C4084727 Cough frequency C0024232 Lymphatic metastasis HSDN C0036572 Convulsion C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C2024878 Cardiovascular surgery result: dyspnea C2945560 Hemolytic HSDN C0398650 Idiopathic thrombocytopenia purpura C0030312 Pancytopenia HSDN C1557397 Adverse event associated with pain C0018081 Gonorrhea HSDN C4084773 Bothered by weight gain C0022104 Irritable bowel syndrome HSDN C0700078 Deep tendon reflex decrease C2750729 Amyotrophic lateral sclerosis 6, autosomal recessive HPO C2364111 Gustatory anesthesia C0035468 Scleroma HSDN C2242996 Tingling C0342700 Cobalamin pseudodeficiency due to transcobalamin deficiency MalaCards C3539892 Pelvic pain in front C2984289 Melanoma pathway HSDN C3898969 Have been vomiting C0338480 Common migraine HSDN C4085317 Diarrhea frequency C0560694 Bottles per feed HSDN C4084802 Usual severity diarrhea C0035078 Kidney failure HSDN C4084767 Bothered by vomiting C0007762 Cerebellar neoplasms HSDN C0162835 Hypopigmentation C0036420 Localized scleroderma OrphaNet|MalaCards C1962972 Proteinuria adverse event C0850803 Anaphylaxis (non medication) HSDN C0587246 Extremity weakness C0410190 Autosomal dominant emery-dreifuss muscular dystrophy (disorder) HPO C0036572 Convulsion C3661618 Myoclonic astatic epilepsy, non-intractable UMLS C0917816 Deficiency mental C2931286 Mosaic variegated aneuplody microcephaly syndrome OrphaNet|HPO|MalaCards C0242936 Center pain C0020502 Hyperparathyroidism HSDN C0020615 Hypoglycemia nos C4015710 Tenorio syndrome MalaCards C3641756 Have diarrhea C0031873 Pica disease HSDN C0011991 Loose stools C0013575 Ectodermal dysplasia HSDN C0036572 Convulsion C0027121 Myositis HSDN C0013604 Edematous C0024586 Malignant carcinoid syndrome HSDN C4084784 Diarrhea C0020179 Huntington disease HSDN C0020672 Body temperature decreased C0344315 Depressed mood HSDN C0043094 Weight gain C1535939 Pneumocystis jiroveci pneumonia HSDN C0040822 D tremors C0342257 Complications of diabetes mellitus HSDN C4084723 Constipation C0020295 Hydronephrosis HSDN C4084784 Diarrhea C0019911 Hookworm infections HSDN C1962972 Proteinuria adverse event C1691228 Cystic kidney diseases HSDN C0002962 Angina C0042974 Von willebrand disease HSDN C0024032 Birth weight subnormal C0175693 Russell-silver syndrome MalaCards|HPO C1963170 Hypothermia adverse event C0002351 Altitude sickness HSDN C0917816 Deficiency mental C2751312 Bartter syndrome, type 4b HPO C4085222 Nausea C0004935 Animal ethology HSDN C0013404 Respiratory difficulty C0152264 Familial erythrocytosis OrphaNet C0022107 Fussiness C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C1963137 Hydrocephalus adverse event C1622510 Neurocytoma MalaCards C4084775 Usual severity weight loss C0700208 Acquired scoliosis HSDN C4085642 Level of joint stiffness C0751278 Metachromatic leukodystrophy, infant MalaCards C0018681 Headache, cephalalgia C0271001 Siderosis of eye HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013990 Pathological accumulation of air in tissues HSDN C0812426 Kidney problem C0748319 Renal insufficiency unilateral UMLS C4084727 Cough frequency C0007621 Neoplastic cell transformation HSDN C4085317 Diarrhea frequency C0024895 Bovine mastitis HSDN C3539022 Pelvic pain decreasing in severity C0409354 Flexion contracture of hip HSDN C1963249 Tinnitus adverse event C0007798 Cerebral ventricle neoplasm HSDN C0030486 Extremity paralysis, lower C1963083 Cholecystitis adverse event HSDN C0848203 Male pelvic pain C1000483 Genus anemia HSDN C2911645 Weight loss adverse event C0036974 Shock HSDN C4085549 Dizziness C0032914 Pre-eclampsia HSDN C4042891 Sleep wake disorders C0003838 Arterial occlusive diseases HSDN C0030486 Extremity paralysis, lower C0031046 Pericarditis HSDN C3539022 Pelvic pain decreasing in severity C0020517 Hypersensitivity HSDN C4085661 Usual severity nausea C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4084768 Usual severity vomiting C0023269 Leiomyosarcoma HSDN C0007758 Cerebellar ataxia C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C0030193 Sense of pain C0243013 Base learn problems HSDN C0018991 Paralysis one side of body C0018564 Hand deformities HSDN C1145670 Failure respiratory C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C3146279 Coma C1863844 Adult-onset citrullinemia type 2 HPO C0043094 Weight gain C0030500 Animal parasitic disease HSDN C3463815 Feel fatigue C0015732 Fecal incontinence HSDN C2237041 Shox gene with short stature C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C0020305 Fetal edema C0038833 Superior vena cava syndrome HSDN C3539895 Pelvic pain occurs with bowel movement C0000768 Congenital abnormality HSDN C4085211 Pain distress question C0022353 Neonatal jaundice HSDN C0518090 Frequency of pain question C0333641 Atrophic HSDN C0013604 Edematous C1963067 Atrial fibrillation adverse event HSDN C0036572 Convulsion C3826393 Epilepsy in mother complicating pregnancy UMLS C2911645 Weight loss adverse event C0024299 Lymphoma HSDN C0023015 Language handicap C4049644 Depression HSDN C0036572 Convulsion C0265329 Organoid nevus phakomatosis OrphaNet|HPO C0013362 Dysarthrias C0333596 Deposition of iron HSDN C3815497 Cough C0008628 Chromosome deletion HSDN C0036659 Sensation disorder C0009395 Color perception HSDN C1963249 Tinnitus adverse event C1847319 Paraganglioma and gastric stromal sarcoma OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0039494 Temporomandibular joint disorders HSDN C0522224 Palsied C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4085862 Bothered by nausea C0268647 Lysinuric protein intolerance MalaCards|HPO C0042940 Disorder of voice C0026946 Mycoses HSDN C0162835 Hypopigmentation C0015624 Fanconi syndrome HPO C0030554 Abnormal sensation C0030489 Paraproteinemias HSDN C4049644 Depression C0001529 Dercum disease OrphaNet|MalaCards C3887873 Hearing loss C0037199 Sinusitis HSDN C0000737 Abdomen pain C0035243 Respiratory tract infections HSDN C0026205 Pupillary constriction C1862441 Ataxia, spastic, with congenital miosis MalaCards C0030552 Paralysis partial C0040038 Thromboembolism HSDN C4084776 Weight loss C0400822 Colitis, lymphocytic HSDN C4085210 Usual severity pain C0003624 Appetitive behavior HSDN C3829611 Nausea frequency C0007786 Brain ischemia HSDN C0009806 Constipate C1546635 Specimen source codes - fistula HSDN C0232943 Metromenorrhagia C3463916 Complement factor i (c3 inactivator) deficiency MalaCards C1963252 Tremor adverse event C1970198 Mental retardation, autosomal recessive 6 HPO C0015672 Decreased energy C0025202 Melanoma HSDN C0026838 Spasticity muscle C0268225 Aspartylglucosaminuria MalaCards|HPO|UMLS C4084776 Weight loss C1956390 Cranial arteritis MalaCards C0575081 Abnormal gait C0268272 Gangliosidosis, generalized gm1, type 2 MalaCards|HPO C0151786 Weakness muscle C0021432 Infratentorial neoplasms HSDN C0009806 Constipate C0011265 Presenile dementia HSDN C0041105 Jaw spasm C0024958 Maxillary sinus neoplasms HSDN C1963252 Tremor adverse event C0008924 Cleft lip HSDN C0018681 Headache, cephalalgia C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C0018772 Deafness C0014070 Encephalomyelitis HSDN C0020538 Hbp C1851286 Ectopia lentis isolated MalaCards|HPO C2315100 Pediatric failure to thrive C0023801 Lipomatosis HSDN C0026884 Muteness C1846130 Mental retardation x-linked, south african type OrphaNet|HPO C0009080 Finger clubbing C0037268 Skin abnormalities MalaCards C0917816 Deficiency mental C1854108 Cerebrooculonasal syndrome OrphaNet|MalaCards C0036659 Sensation disorder C0027651 Tumor HSDN C0003962 Ascites C1856303 Gsd iv, neuromuscular form, fatal perinatal HPO C2029884 Hearing loss by exam C1510460 Orofaciodigital syndrome i MalaCards C0917816 Deficiency mental C0796063 Microcephaly-digital anomalies syndrome MalaCards C0424755 Fever symptoms C0026113 Heat rash HSDN C0013421 Dystonia C0018671 Head and neck neoplasms HSDN C0010520 Skin cyanosis C0032344 Poisoning aspects HSDN C4084725 Usual severity cough C0019693 Hiv infections HSDN C0231218 Malaise generalized C0031903 Pigeon breeder's lung MalaCards C0026826 High muscle tone C1327916 Revesz syndrome (disorder) MalaCards|HPO C0007166 Cardiac output decreased C0024141 Lupus erythematosus, systemic HSDN C0000737 Abdomen pain C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0018681 Headache, cephalalgia C0018939 Hematological disease HSDN C0231791 In toe C1859406 Borrone di rocco crovato syndrome MalaCards C0036572 Convulsion C3554385 Congenital disorder of glycosylation, type iu MalaCards C0018681 Headache, cephalalgia C0949760 Personal autonomy HSDN C0007758 Cerebellar ataxia C0393590 Fahr's syndrome (disorder) MalaCards|UMLS C0332563 Papulae C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards C0039231 Heartbeats increased C2936913 Porphyria, south african type HPO C1963087 Constipation adverse event C1263846 Attention deficit hyperactivity disorder HSDN C3665347 Vision impaired C0206245 Amyloid neuropathies, familial MalaCards C4084742 Bothered by night sweats C0220620 Gastrointestinal carcinoid tumor MalaCards C1963177 Muscle pain adverse event C1849386 Myoglobinuria, acute recurrent, autosomal recessive MalaCards C0011991 Loose stools C0037933 Spinal diseases HSDN C0026603 Motion sickness C0037369 Smoking HSDN C0037384 Snore C0597384 Respiratory airflow disorder UMLS C1963065 Apnea adverse event C0042138 Uterine neoplasms HSDN C0031911 Pigment deposition C0012243 Digestive system neoplasms MalaCards C4084774 Have weight loss C0010356 Cross infection HSDN C1963281 Vomiting adverse event C0015726 Focused anxiety HSDN C0034155 Thrombotic thrombocytopenic purpura C0702094 Agranulocytosis lab result HSDN C4085661 Usual severity nausea C0001430 Adenoma HSDN C0232466 Feeding difficulty C3281138 Chromosome 17q12 deletion syndrome MalaCards C0242936 Center pain C0024692 Mandible fracture HSDN C4085548 Usual severity dizziness C0700327 Clinical findings relating to memory HSDN C2025995 Cellulitis C0008628 Chromosome deletion MalaCards C0010200 Cough symptom C0264353 Bronchomalacia HSDN C3541349 Syncope C2678476 Cardiomyopathy, dilated, 1y MalaCards C1963077 Bone pain adverse event C1845168 Hypophosphatemic rickets, x-linked recessive MalaCards|HPO C0018991 Paralysis one side of body C0264305 Laryngeal hemiplegia UMLS C0349588 Stature short C4015495 Cerebellofaciodental syndrome MalaCards C4085211 Pain distress question C0018816 Heart septal defects HSDN C0151786 Weakness muscle C0037379 Snake bite HSDN C0018681 Headache, cephalalgia C0017589 Farcy DiseaseOntology|MalaCards C4084769 Vomiting frequency C0043167 Pertussis HSDN C0042571 Vertigo subjective C0026782 Mumps vaccine HSDN C1145670 Failure respiratory C0023176 Lead poisoning MalaCards C0518090 Frequency of pain question C0751878 Vasculitis, central nervous system HSDN C0013404 Respiratory difficulty C0854993 Lung squamous cell carcinoma stage iii UMLS C0557874 Global developmental delay C0023521 Globoid cell leukodystrophy OrphaNet C4084766 Vomiting C0078981 Arachnoid cysts HSDN C0011991 Loose stools C1762616 Meningioma, benign, no icd-o subtype HSDN C3274924 Have been coughing C1836929 Emanuel syndrome MalaCards C0026826 High muscle tone C3806917 Craniosynostosis 4 MalaCards C1963071 Back pain adverse event C0015379 Extravasation of diagnostic and therapeutic materials HSDN C0085636 Light sensitivity C0010038 Corneal opacity HSDN C0032617 High urine output C0011880 Diabetic ketoacidosis UMLS C1963137 Hydrocephalus adverse event C0795953 Masa syndrome (disorder) MalaCards|HPO C0009421 Comatose C0036601 Self mutilation HSDN C3203358 Alveolar hypoventilation C0030353 Papilledema HSDN C0015468 Face pain C0022410 Joint instability HSDN C1963249 Tinnitus adverse event C3888076 Deafness, y-linked 1 MalaCards C4042891 Sleep wake disorders C0043254 Injuries penetrating HSDN C0033790 Pseudobulbar palsy C0004045 Asphyxia neonatorum HSDN C0241210 Speaking delay C2675369 Chromosome 22q11.2 microduplication syndrome OrphaNet|HPO C0038990 Sweats C3203358 Hypoventilation MalaCards C0013404 Respiratory difficulty C0346647 Malignant neoplasm of pancreas UMLS C0011175 Deficient fluid volume C0010674 Cystic fibrosis MalaCards|HPO C0013421 Dystonia C4015261 Polyendocrine-polyneuropathy syndrome MalaCards C4085211 Pain distress question C0011269 Dementia, vascular HSDN C0700072 Encounter due to stillbirth C1848600 Vater association with hydrocephalus HPO C0151786 Weakness muscle C0853697 Neutrophil count decreased HSDN C1304408 Urticarial vasculitis C0021385 Inflammation, necrotizing UMLS C0022346 Yellow skin C0024788 Green monkey virus disease OrphaNet|MalaCards C1963170 Hypothermia adverse event C0014121 Bacterial endocarditis HSDN C0242936 Center pain C0008513 Chorioretinitis HSDN C4085211 Pain distress question C0016667 Fragile x syndrome HSDN C0522224 Palsied C3163620 Hypotension adverse event HSDN C0086565 Liver function abnormal C3542026 Peroxisome biogenesis disorder 5b MalaCards C1384666 Decreased hearing C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0036572 Convulsion C3150700 Mental retardation, autosomal dominant 20 HPO|UMLS C0036572 Convulsion C0021933 Intussusception HSDN C2919142 Short stature adverse event C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism OrphaNet|MalaCards C3463815 Feel fatigue C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C2919142 Short stature adverse event C1862381 Auriculo-osteodysplasia OrphaNet|MalaCards C4084726 Distress cough C0035078 Kidney failure HSDN C0018991 Paralysis one side of body C0432201 Boomerang dysplasia MalaCards C4084802 Usual severity diarrhea C0027022 Myeloproliferative disease HSDN C4042891 Sleep wake disorders C4042938 Injuries, war-related HSDN C0349588 Stature short C4014954 Neutropenia, severe congenital, 6, autosomal recessive MalaCards C0015672 Decreased energy C0010709 Cyst HSDN C0000737 Abdomen pain C0034186 Pyelonephritis HSDN C0278152 Hemifacial spasms C0431399 Familial aplasia of the vermis MalaCards|HPO C0151686 Growth retardation C0024814 Marinesco-sjogren syndrome MalaCards C0000727 Abdomen acute C1456865 Ureteral calculi HSDN C4085862 Bothered by nausea C0021799 Interprofessional relations HSDN C0027066 Myoclonic jerking C0027849 Neuroleptic malignant syndrome HSDN C0033774 Skin pruritus C1299262 Sarcoma - category (morphologic abnormality) HSDN C0018772 Deafness C0018923 Hemangiosarcoma HSDN C1961131 Cough adverse event C0003467 Anxiety HSDN C0009421 Comatose C0018809 Heart neoplasm HSDN C3539889 Pelvic pain increasing in severity C2936403 46, xx disorders of sex development HSDN C0002170 Alopecia disorders C2750285 Progeria syndrome, childhood-onset HPO C0036572 Convulsion C0007177 Cardiac tamponade HSDN C3463815 Feel fatigue C0687150 Parathyroid gland adenocarcinoma OrphaNet|HPO|MalaCards C0009421 Comatose C1855369 Maple syrup urine disease, type ia HPO C1962972 Proteinuria adverse event C3163620 Hypotension adverse event HSDN C0040822 D tremors C0009324 Ulcerative colitis HSDN C0018834 Brash C1836929 Emanuel syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0036216 Sarcoma, experimental HSDN C3829611 Nausea frequency C0042830 Perception visual HSDN C0015672 Decreased energy C0043167 Pertussis HSDN C3641756 Have diarrhea C0241910 Hepatitis, autoimmune HSDN C4084788 Have dizziness C1547940 Specimen source codes - ulcer HSDN C2362324 Pediatric obesity C0010068 Coronary heart disease HSDN C0042571 Vertigo subjective C0027686 Pathologic neovascularization HSDN C0018777 Deafness, conductive C0019522 Adenoma, sweat gland HSDN C4085862 Bothered by nausea C0027831 Neurofibromatosis 1 HSDN C0018991 Paralysis one side of body C3648310 Late effects of cerebral infarction hemiplegia UMLS C4085661 Usual severity nausea C1963084 Colitis adverse event HSDN C2073625 X-ray of chest: pleural effusion C2931146 Radio renal syndrome MalaCards C4084802 Usual severity diarrhea C0085389 Bacillaceae infection HSDN C2024878 Cardiovascular surgery result: dyspnea C0241158 Cicatrix skin HSDN C0005779 Clotting C3553597 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome MalaCards C0009806 Constipate C1709867 Rectosigmoid mucinous adenocarcinoma UMLS C0413252 Hypothermia due to exposure C0016057 Fibrosarcoma HSDN C0011991 Loose stools C0030299 Pancreatic pseudocyst HSDN C0043094 Weight gain C0007682 Cns disorder HSDN C0026821 Cramp C0024591 Malignant hyperpyrexia due to anesthesia HSDN C1549543 Administration method - pain C0007868 Cervical dysplasia HSDN C0013404 Respiratory difficulty C0025202 Melanoma HSDN C4049644 Depression C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0036572 Convulsion C2931242 Familial waldmann's disease MalaCards C1963252 Tremor adverse event C0029456 Osteoporosis HSDN C0018524 Hallucinate C0019829 Hodgkin disease HSDN C0040034 Thrombocytopenia C0017205 Gaucher disease OrphaNet|MalaCards C0009676 Confusion state C0276496 Familial alzheimer disease (fad) MalaCards C0015672 Decreased energy C0007222 Cardiovascular diseases HSDN C4084773 Bothered by weight gain C0011253 Delusions HSDN C4042861 Benign obesity, metabolically C0023676 Life style HSDN C0030975 Disorders perception C0006107 Concussion HSDN C1963065 Apnea adverse event C0009953 Convulsive therapy HSDN C0917816 Deficiency mental C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C4084802 Usual severity diarrhea C0040582 Trachea neoplasm HSDN C0010038 Corneal opacity disorder C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C4084802 Usual severity diarrhea C0024694 Mandibular neoplasms HSDN C4084773 Bothered by weight gain C0011071 Sudden death HSDN C3274924 Have been coughing C0004161 Athletic injuries HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023772 Lipid metabolism, inborn errors HSDN C1557397 Adverse event associated with pain C0037052 Sick sinus syndrome HSDN C4085222 Nausea C1690964 Cataract HSDN C3815497 Cough C0220981 Metabolic acidosis HSDN C0011991 Loose stools C0155862 Streptococcal pneumonia HSDN C0020673 Hypothermia (central) (local) C0026848 Myopathy HSDN C4085211 Pain distress question C0029106 Opisthorchiasis HSDN C3146279 Coma C0007097 Carcinomas HSDN C0232943 Metromenorrhagia C0043398 Yellow fever, urban MalaCards C0575081 Abnormal gait C0342751 Generalized glycogen storage disease of infants MalaCards C0027796 Neuralgias C2711227 Steatohepatitis HSDN C0518090 Frequency of pain question C0013504 Echinococcosis, hepatic HSDN C4085210 Usual severity pain C0032897 Prader-willi syndrome HSDN C4084802 Usual severity diarrhea C0001139 Acinetobacter infection HSDN C4085211 Pain distress question C0206623 Adenosquamous carcinoma HSDN C0270948 Neurogenic muscular atrophy C2678471 Lethal arthrogryposis with anterior horn cell disease HPO C4084802 Usual severity diarrhea C1859407 Bone dysplasia, lethal, holmgren type MalaCards C1557397 Adverse event associated with pain C0020452 Hyperemia HSDN C3665492 Pigmentations C0162834 Hyperpigmentation MalaCards C0015230 Exanthem C0857192 Rash trunk & limbs UMLS C1549543 Administration method - pain C0025490 Mesonephroma HSDN C0424755 Fever symptoms C0038187 Starvation HSDN C0727671 Red cross toothache drops C0040438 Ectopic tooth eruption HSDN C1279888 Proteinuria of undiagnosed cause C0038354 Stomach diseases HSDN C1549543 Administration method - pain C0020876 Ileal neoplasms HSDN C0000737 Abdomen pain C0032914 Pre-eclampsia HSDN C0042963 Symptoms vomiting C0038000 Spleen rupture HSDN C3898969 Have been vomiting C0393735 Headache disorders HSDN C2919142 Short stature adverse event C1859711 Arthrogryposis multiplex congenita with whistling face OrphaNet|MalaCards C0022346 Yellow skin C0018273 Growth disorders HSDN C0242936 Center pain C0039231 Tachycardia HSDN C0010038 Corneal opacity disorder C4013035 Brain small vessel disease with or without ocular anomalies MalaCards C0036396 Sciatica C0031117 Peripheral neuropathy UMLS C0026821 Cramp C3714933 Myopathy due to myoadenylate deaminase deficiency MalaCards C0036572 Convulsion C0005686 Urinary bladder diseases HSDN C0015469 Facial paralysis C0039730 Thalassemia HSDN C4085210 Usual severity pain C1510502 Oxyphilic adenoma HSDN C0038990 Sweats C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C1963086 Confusion adverse event C0019693 Hiv infections HSDN C0036572 Convulsion C0158266 Intervertebral disc degeneration HSDN C1069915 Vertigo C0010054 Coronary arteriosclerosis HSDN C4084725 Usual severity cough C0019270 Hernia HSDN C0040485 Wryneck C0005745 Blepharoptosis HSDN C4085317 Diarrhea frequency C0009862 Contraception behavior HSDN C0026838 Spasticity muscle C0019557 Hip fx HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1009209 Tinea HSDN C0041657 Consciousness loss C0011880 Diabetic ketoacidosis HSDN C1557397 Adverse event associated with pain C0024961 Injuries maxillofacial HSDN C0006370 Bulimia C0036601 Self mutilation HSDN C0020673 Hypothermia (central) (local) C2936490 Cardiac arrest, out-of-hospital HSDN C0917816 Deficiency mental C1859726 Arterial tortuosity syndrome MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0035126 Reperfusion injury HSDN C0020450 Hyperemesis gravidarum C1535926 Neurodevelopmental disorders HSDN C0162835 Hypopigmentation C1847836 Oculocutaneous albinism, type iv OrphaNet|MalaCards C2203646 Jaundice C1258104 Diffuse scleroderma HSDN C0015672 Decreased energy C0013926 Aeroembolism HSDN C0013395 Indigestion C2984299 Asthma pathway HSDN C2984058 Have pain C2616767 Mycetoma HSDN C0015970 Fever unknown origin C0042065 Genitourinary neoplasms HSDN C4085222 Nausea C0042345 Varicosity HSDN C0038002 Spleen enlargement C0018203 Chronic granulomatous disease MalaCards|HPO C0917816 Deficiency mental C0796137 3c syndrome OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0020542 Pulmonary hypertension HSDN C0009806 Constipate C0007820 Cerebrovascular disorders HSDN C1963087 Constipation adverse event C1962986 Glaucoma adverse event HSDN C1963252 Tremor adverse event C0036974 Shock HSDN C4084775 Usual severity weight loss C0015726 Focused anxiety HSDN C0575081 Abnormal gait C0268242 Niemann-pick disease, type a MalaCards C0007398 Catatonic C0033968 Psychotherapeutic technique HSDN C2096293 Ent surgical result ear vertigo C1963064 Anxiety adverse event HSDN C0026821 Cramp C0149931 Migraine disorders HSDN C0497247 Blood pressure elevation C0013364 Dysautonomia, familial OrphaNet|HPO C1963064 Anxiety adverse event C1858501 Spinocerebellar ataxia 12 MalaCards|HPO C0004134 Dyssynergia C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards|UMLS C4084776 Weight loss C0036946 Sheep--diseases HSDN C2237041 Shox gene with short stature C1859967 Agonadism dextrocardia diaphragmatic hernia MalaCards C0557874 Global developmental delay C3809356 Multiple congenital anomalies-hypotonia-seizures syndrome 3 MalaCards C0018524 Hallucinate C0039538 Teratoma HSDN C0008031 Pain chest C0036117 Salmonella infections HSDN C0018681 Headache, cephalalgia C0460136 Barotrauma HSDN C0002962 Angina C0702166 Acne HSDN C0030200 Intractable pain C3813607 Infantile gastroesophageal reflux HSDN C0013395 Indigestion C0030297 Pancreatic neoplasm HSDN C0474368 Childbirth pain C0079924 Oligohydramnios HSDN C3463815 Feel fatigue C1532253 Sedentary lifestyle HSDN C2127523 Left hand atrophy C1290871 Disorder of hand UMLS C1961131 Cough adverse event C0019621 Histiocytosis, langerhans-cell HSDN C4084766 Vomiting C0020443 Hypercholesterolemia HSDN C2032396 Pelvic pain on the right C0432264 Axial osteosclerosis MalaCards C2029884 Hearing loss by exam C0524910 Hepatitis c, chronic HSDN C0851578 Disorder sleep C0039231 Tachycardia HSDN C4085642 Level of joint stiffness C0086649 Mps iii c HPO C0859060 Hypobulia (abulia) C0919974 Abulia UMLS C3898969 Have been vomiting C0009241 Cognition disorders HSDN C0007758 Cerebellar ataxia C0007781 Intracranial embolism and thrombosis HSDN C0027497 Queasy C0003078 Aniseikonia HSDN C0042024 Urine incontinence C0001807 Aggressive behavior HSDN C0040822 D tremors C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C4085862 Bothered by nausea C1253943 Fluid in the chest HSDN C2242996 Tingling C0019693 Hiv infections HSDN C0003962 Ascites C0031069 Familial mediterranean fever HPO C0557874 Global developmental delay C0175695 Sotos' syndrome OrphaNet|HPO|MalaCards C0022346 Yellow skin C3888385 Peroxisome biogenesis disorder 7a (zellweger) MalaCards C2919142 Short stature adverse event C3469606 Pseudohypoaldosteronism, type iie MalaCards C0001707 Aerophagia C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C3463815 Feel fatigue C0314657 Genetic predisposition HSDN C0000737 Abdomen pain C0035012 Reiter syndrome OrphaNet|MalaCards C0018772 Deafness C0456892 Csf low pressure HSDN C0034151 Hyperglobulinemic purpura C1138434 Disease, x-linked genetic HSDN C0024031 Back pain lower back C0034530 Injury radiation HSDN C4084725 Usual severity cough C0009651 Conditioning operant HSDN C0150055 Pain chronic C0343267 Hand reflex sympathetic dystrophy UMLS C1963252 Tremor adverse event C3813607 Infantile gastroesophageal reflux HSDN C0009792 Consciousness disorder C0024291 Lymphohistiocytosis, hemophagocytic HSDN C1962972 Proteinuria adverse event C0272375 Antithrombin iii deficiency HSDN C4085211 Pain distress question C1415701 Hprt1 gene HSDN C2024893 Cardiovascular surgery result: fatigue C0031149 Peritoneal neoplasms HSDN C4084775 Usual severity weight loss C0600260 Lung diseases, obstructive HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C4085635 Appetite quality question HSDN C3641756 Have diarrhea C0026780 Mumps HSDN C4085317 Diarrhea frequency C1959626 Mevalonic aciduria MalaCards|HPO C0016204 Fart C0036239 Satiety HSDN C4084768 Usual severity vomiting C0752132 Infarction, pca HSDN C0020580 Decreased sensation C1962979 Burn adverse event HSDN C3887638 Failure to thrive in infant C1859538 Bare lymphocyte syndrome, type ii, complementation group e HPO C1557397 Adverse event associated with pain C1879737 Aromatherapy and essential oils HSDN C0007758 Cerebellar ataxia C0004936 Mental disorders HSDN C0030232 Color loss C0042880 Vitamin k deficiency HSDN C0018681 Headache, cephalalgia C1414203 Dws gene HSDN C0151740 Intracranial hypertension C2931270 Craniodiaphyseal dysplasia, dominant MalaCards C0030193 Sense of pain C0020625 Hyponatremia HSDN C0234146 Absent reflex C0751540 Morvan disease HPO C3463815 Feel fatigue C0029927 Ovarian cysts HSDN C0018965 Blood urine C0022739 Klippel-trenaunay-weber syndrome MalaCards C0027497 Queasy C4049644 Depression HSDN C1069915 Vertigo C0027686 Pathologic neovascularization HSDN C0002962 Angina C0026857 Musculoskeletal diseases HSDN C0013362 Dysarthrias C3179088 Injuries, lingual nerve HSDN C0015469 Facial paralysis C0041107 Trisomy HSDN C0003469 Anxiety disorder C0796237 Mental retardation, x-linked 30 HPO C1963091 Diarrhea adverse event C0032708 Disorders of porphyrin metabolism OrphaNet|HSDN|MalaCards C0015469 Facial paralysis C0018671 Head and neck neoplasms HSDN C4084725 Usual severity cough C0152018 Esophageal carcinoma OrphaNet|MalaCards C4084784 Diarrhea C0221056 Adult type dermatomyositis HSDN C0010200 Cough symptom C1334788 Combined small cell and squamous cell lung carcinoma UMLS C0018681 Headache, cephalalgia C0036983 Septic shock HSDN C0221166 Paraparesis C0221065 Subacute combined degeneration HSDN C0427068 Legs weakness C2931821 Nakamura osame syndrome MalaCards C4084726 Distress cough C0085232 Diverticulum zenker HSDN C0424755 Fever symptoms C0752235 Lyme neuroborreliosis DiseaseOntology|MalaCards C4084784 Diarrhea C0870082 Hyperkeratosis HSDN C4085548 Usual severity dizziness C0041582 Ulcer HSDN C1971624 Appetite absent C0007134 Renal cell carcinoma HSDN C0011175 Deficient fluid volume C1857395 De toni-debre-fanconi syndrome HPO C0022346 Yellow skin C0038013 Ankylosing spondylitis HSDN C0036572 Convulsion C0221355 Macrocephaly HSDN C0018772 Deafness C0003646 Aptitude HSDN C3274924 Have been coughing C2931916 Midline granulomatosis MalaCards C1963281 Vomiting adverse event C0023817 Hyperlipoproteinemia type i HPO C1963249 Tinnitus adverse event C4048184 Trochlear nerve diseases HSDN C0151786 Weakness muscle C0032268 Pneumocephalus HSDN C0003079 Pupillary inequality C0027743 Nerve compression syndrome HSDN C3641756 Have diarrhea C1270972 Mild cognitive disorder HSDN C0042024 Urine incontinence C2219717 Menstrual periods stopped for over 6 months HSDN C0009806 Constipate C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO C4084775 Usual severity weight loss C0205788 Histiocytoid hemangioma HSDN C0152169 Colic renal C0810321 Other and unspecified urinary calculus UMLS C2315100 Pediatric failure to thrive C0001173 Adult pyloric stenosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0029443 Osteomyelitis HSDN C2096293 Ent surgical result ear vertigo C0037952 Spinocerebellar degeneration HSDN C1549543 Administration method - pain C0013240 Alveolar osteitis HSDN C1999266 Depression adverse event C3150344 Hyperhomocysteinemia, thrombotic, cbs-related HPO C0851578 Disorder sleep C0037933 Spinal diseases HSDN C0042963 Symptoms vomiting C0015401 Foreign body in eye HSDN C3898969 Have been vomiting C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C0039070 Collapse fleeting C0037929 Spinal cord injuries HSDN C0043094 Weight gain C0032231 Pleurisy HSDN C0155344 Spasm of conjugated gaze C2063486 Disorders of gaze UMLS C4084726 Distress cough C0032298 Lipid pneumonia HSDN C0033774 Skin pruritus C0206141 Idiopathic hypereosinophilic syndrome HSDN|HPO|UMLS C0042571 Vertigo subjective C0271493 Angiospastic ophthalmo-auricular syndrome UMLS C2315100 Pediatric failure to thrive C0206762 Limb deformities, congenital HSDN C2203646 Jaundice C0006145 Breast diseases HSDN C4084775 Usual severity weight loss C1527311 Brain edema HSDN C0424755 Fever symptoms C0007820 Cerebrovascular disorders HSDN C1557397 Adverse event associated with pain C0022729 Klebsiella infections HSDN C0277959 Hair coarseness C2931597 Macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance MalaCards C0018989 Paresis of one side of body C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0423729 Breath chest pain C0810021 Other lower respiratory disease UMLS C0001707 Aerophagia C0039231 Tachycardia HSDN C0917816 Deficiency mental C3809686 Mental retardation, autosomal dominant 21 MalaCards C0349588 Stature short C0878683 Pituitary dwarfism type 3 MalaCards|HPO C2984058 Have pain C0014553 Absence epilepsy HSDN C0012833 Dizzy C0003813 Arrhythmia sinus HSDN C0000737 Abdomen pain C0024523 Malabsorption syndrome HSDN C4084788 Have dizziness C2911643 Encounter due to family history of osteoporosis HSDN C4084788 Have dizziness C1963064 Anxiety adverse event HSDN C0242936 Center pain C0004659 Bacteriuria HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0043246 Laceration HSDN C4084802 Usual severity diarrhea C0162557 Liver failure, acute HSDN C4084725 Usual severity cough C0597109 Nurse's role HSDN C0231613 Headache occipital C0003803 Arnold chiari malformation MalaCards C4085211 Pain distress question C0019364 Herpes zoster ophthalmicus HSDN C2024878 Cardiovascular surgery result: dyspnea C0024620 Primary malignant neoplasm of liver MalaCards C0018784 Deafness sensorineural C2931587 Gemignani syndrome OrphaNet|MalaCards C0030552 Paralysis partial C0003615 Appendicitis HSDN C0242936 Center pain C0006285 Bronchopneumonia HSDN C4084767 Bothered by vomiting C0524909 Hepatitis b, chronic MalaCards C0557874 Global developmental delay C0015393 Eye abnormalities MalaCards C1963281 Vomiting adverse event C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C4084784 Diarrhea C0235387 Porphyria type syndrome OrphaNet C0039070 Collapse fleeting C0009651 Conditioning operant HSDN C0242936 Center pain C0080274 Urinary retention HSDN C2187990 Unable to perform sex C0393911 Pure autonomic failure MalaCards C1549543 Administration method - pain C0038358 Gastric ulcer HSDN C1963252 Tremor adverse event C1861848 Paragangliomas 4 MalaCards C0030193 Sense of pain C0016412 Folic acid deficiency HSDN C0030486 Extremity paralysis, lower C0021655 Insulin resistance HSDN C0020903 Illusion C0033911 Applied psychology HSDN C0009421 Comatose C0268595 Glutaric aciduria, type 1 HPO C0042963 Symptoms vomiting C1548484 Rheumatic fever vaccine HSDN C0042963 Symptoms vomiting C0344434 Atrial fibrillation ecg HSDN C3274924 Have been coughing C0003962 Ascites HSDN C0231678 Ulnar deviation of the wrists C0086652 Mucopolysaccharidosis type ivb HPO|UMLS C0042963 Symptoms vomiting C0018805 Heart injuries HSDN C4084774 Have weight loss C1610547 Production class code - pleasure HSDN C0009806 Constipate C3683846 Chromosome 17p deletion syndrome MalaCards C3641756 Have diarrhea C0032371 Poliomyelitis HSDN C1549543 Administration method - pain C0001429 Adenolymphoma HSDN C2024893 Cardiovascular surgery result: fatigue C0001529 Dercum disease OrphaNet|MalaCards C0040485 Wryneck C0007798 Cerebral ventricle neoplasm HSDN C4084725 Usual severity cough C0036117 Salmonella infections HSDN C4084784 Diarrhea C0700095 Central neuroblastoma MalaCards|HSDN C0000737 Abdomen pain C0007785 Cerebral infarction HSDN C4042891 Sleep wake disorders C0038271 Stereotyped behavior HSDN C0162834 Hyperpigmentation C0151467 Addisonian crisis OrphaNet|MalaCards C4085317 Diarrhea frequency C0030469 Paranasal sinus diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C0005695 Bladder neoplasm HSDN C1549543 Administration method - pain C0020619 Hypogonadism HSDN C3641756 Have diarrhea C0030500 Animal parasitic disease HSDN C4085210 Usual severity pain C0043251 Wounds and injuries HSDN C0011206 Delirium acute C0026764 Multiple myeloma HSDN C0036572 Convulsion C0015618 Families therapy HSDN C0264272 Nose discharge, purulent C0041912 Upper respiratory infections UMLS C0010200 Cough symptom C0014859 Esophageal neoplasms OrphaNet|HSDN|MalaCards C4085211 Pain distress question C0162836 Hidradenitis suppurativa HSDN C4084766 Vomiting C0007131 Non-small cell lung carcinoma HSDN C0013604 Edematous C0151699 Intracranial hemorrhages HSDN C0557874 Global developmental delay C0796202 Wittwer syndrome MalaCards C0027497 Queasy C0018552 Hamartoma HSDN C1549543 Administration method - pain C0026766 Multiple organ failure HSDN C0004604 Pain back C0034885 Rectal neoplasms HSDN C0003550 Broca aphasia C1962958 Hematoma adverse event HSDN C0522224 Palsied C0012979 Canine disease HSDN C3539890 Pelvic pain causes awakening at night C0010692 Cystitis HSDN C4085661 Usual severity nausea C0024117 Chronic obstructive airway disease HSDN C0019572 Hairiness C0031090 Periodontal diseases HSDN C0037763 Spasm C0036864 Sexual relations HSDN C4084769 Vomiting frequency C3661523 Congenital intestinal aganglionosis MalaCards C0036572 Convulsion C0795934 Digitorenocerebral syndrome UMLS C0700590 Diaphoresis excessive C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0013362 Dysarthrias C0270612 Leukoencephalopathies HSDN C0030552 Paralysis partial C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C0020578 Hyperventilate C0010823 Cytomegalovirus infections HSDN C0857305 Thrombocytopenia purpura C0032463 Polycythemia vera HSDN C0010200 Cough symptom C0011616 Contact dermatitis HSDN C4084724 Usual severity constipation C0268386 Amyloid polyneuropathy, swiss type MalaCards C0027066 Myoclonic jerking C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0035021 Fever, famine C3553937 Pbd4b MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011875 Diabetic angiopathies HSDN C0240991 Sensory ataxia C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating MalaCards C0006370 Bulimia C0038663 Suicide attempt HSDN C2919142 Short stature adverse event C0175691 Dubowitz syndrome OrphaNet|HPO|MalaCards C4085549 Dizziness C0702221 Tactual discrimination HSDN C2984058 Have pain C0018946 Hematoma, subdural HSDN C2919142 Short stature adverse event C1853120 Noonan syndrome 4 MalaCards|HPO C0497406 Over weight C1299262 Sarcoma - category (morphologic abnormality) HSDN C2237041 Shox gene with short stature C0796032 Malpuech facial clefting syndrome MalaCards C4050613 Anxiety C1568248 Usher syndrome, type iii MalaCards|HPO C0518090 Frequency of pain question C0038016 Spondylolisthesis HSDN C4084784 Diarrhea C0032787 Postoperative complications HSDN C0004134 Dyssynergia C0004943 Behcet syndrome MalaCards|HPO C3809715 Epistaxis recurrent C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C4085548 Usual severity dizziness C0348018 Projections HSDN C2237041 Shox gene with short stature C1852513 Coxoauricular syndrome OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0040425 Tonsillitis HSDN C4084802 Usual severity diarrhea C0023895 Liver diseases HSDN C1962972 Proteinuria adverse event C0027659 Neoplasms, experimental HSDN C0151311 Cranial nerve palsy C0752235 Lyme neuroborreliosis MalaCards C0030486 Extremity paralysis, lower C0031090 Periodontal diseases HSDN C3463815 Feel fatigue C1553188 Hemolysis - observation HSDN C0231218 Malaise generalized C2981668 Stage iii distal bile duct cancer UMLS C0024031 Back pain lower back C0334299 Carcinoid tumor no icd-o subtype HSDN C0162275 Ketoaciduria C0268595 Glutaric aciduria, type 1 HPO C4085862 Bothered by nausea C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C4085211 Pain distress question C0022904 Lacrimal apparatus diseases HSDN C2911647 Weight gain adverse event C0852795 Increased insulin level HSDN C0476218 Athetosis, acquired, nos C0392702 Abnormal involuntary movement UMLS C0454644 Delayed language development C3151184 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 MalaCards|HPO C0042963 Symptoms vomiting C0948039 Bacterial gastritis MalaCards C0018784 Deafness sensorineural C0027947 Neutropenia HSDN C1963137 Hydrocephalus adverse event C0010495 Cutis laxa OrphaNet|MalaCards C0391860 Diffuse inflammations C0267645 Idiopathic diffuse ulcerative nongranulomatous enteritis UMLS C0848203 Male pelvic pain C0021359 Infertility HSDN C0013604 Edematous C0021053 Immune system diseases HSDN C4084775 Usual severity weight loss C0020443 Hypercholesterolemia HSDN C0042963 Symptoms vomiting C0013182 Drug allergy HSDN C3641756 Have diarrhea C0014571 Epiphyses, slipped HSDN C4084775 Usual severity weight loss C0007789 Cerebral palsy HSDN C0023014 Developmental disorder language C0018767 Auditory sense HSDN C0848203 Male pelvic pain C0005940 Bone diseases HSDN C0036572 Convulsion C2676254 Prickle1-related progressive myoclonus epilepsy with ataxia UMLS C4084774 Have weight loss C0004659 Bacteriuria HSDN C0022346 Yellow skin C0267792 Hepatobiliary disease UMLS C0009421 Comatose C0595812 Fistula route HSDN C0004134 Dyssynergia C1864112 Huntington disease-like 1 MalaCards|UMLS C4085862 Bothered by nausea C0017152 Gastritis HSDN C0036572 Convulsion C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C0040524 Septic toxemia HSDN C0476273 Distress respiratory C2677362 Alveolar capillary dysplasia OrphaNet|HPO|MalaCards C0028961 Urine output decreased C0242341 Sexual infantilism HSDN C0522224 Palsied C0030353 Papilledema HSDN C0231712 Gait waddling C3279738 Cerebral palsy, spastic quadriplegic, 5, formerly MalaCards|UMLS C0020672 Body temperature decreased C4049994 Insulin resistance measurement HSDN C2911645 Weight loss adverse event C0040336 Tobacco use disorder HSDN C0403569 Pain during outflow of dialysate C1290864 Abdominal disorders UMLS C3815497 Cough C0027092 Myopia HSDN C0009806 Constipate C0019080 Hemorrhage HSDN C0013604 Edematous C0018922 Hemangiopericytoma HSDN C0042963 Symptoms vomiting C0003869 Arthritis, infectious HSDN C2188172 Unexplained vaginal bleeding C0567444 Nonmenstrual bleeding UMLS C0030552 Paralysis partial C0751865 Alcohol-induced disorders, nervous system HSDN C2024893 Cardiovascular surgery result: fatigue C0032285 Pneumonia HSDN C0857305 Thrombocytopenia purpura C0038000 Spleen rupture HSDN C0085631 Abnormal excitement C0009324 Ulcerative colitis HSDN C4084727 Cough frequency C2713321 Alpha-l-iduronidase deficiency OrphaNet C0030552 Paralysis partial C0153136 Oth late congen syph,symptm DiseaseOntology|MalaCards C3463815 Feel fatigue C0021799 Interprofessional relations HSDN C0004604 Pain back C0020428 Hyperaldosteronism HSDN C0013604 Edematous C0020542 Pulmonary hypertension HSDN C4085210 Usual severity pain C0024591 Malignant hyperpyrexia due to anesthesia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0027819 Neuroblastoma HSDN C1963077 Bone pain adverse event C0268251 Gaucher disease, type 3 (disorder) OrphaNet|HPO|MalaCards C1971624 Appetite absent C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C1961131 Cough adverse event C0037930 Spinal cord neoplasms HSDN C0151786 Weakness muscle C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C1549543 Administration method - pain C0025427 Mercury poisoning HSDN C0014724 Burping C0021833 Intestinal fistula HSDN C3829611 Nausea frequency C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0234144 Dysgraphia C1136041 Familial acoustic neuroma HPO C0401149 Constipation chronic C0267509 Constipation chronic idiopathic UMLS C0011991 Loose stools C0268680 Biotin deficiency MalaCards C0040460 Dental pain C0027073 Myofascial pain syndromes HSDN C0242670 Chronic vegetative state C0079631 Interdisciplinary communication HSDN C0522224 Palsied C0702094 Agranulocytosis lab result HSDN C3541349 Syncope C2911643 Encounter due to family history of osteoporosis HSDN C0037763 Spasm C0002170 Alopecia HSDN C0015732 Feces incontinence C2930798 Alexanders leukodystrophy MalaCards C4085211 Pain distress question C0016059 Fibrosis HSDN C0013362 Dysarthrias C0023051 Laryngeal diseases HSDN C0043094 Weight gain C0021845 Intestinal perforation HSDN C0020673 Hypothermia (central) (local) C0013595 Eczema HSDN C4084727 Cough frequency C0007762 Cerebellar neoplasms HSDN C0241165 Skin thickening C0043346 Xeroderma pigmentosum OrphaNet C0028738 Nystagmus C0004135 Ataxia telangiectasia OrphaNet|HPO|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0026896 Myasthenia gravis HSDN C0497406 Over weight C1963198 Pancreatitis adverse event HSDN C0518090 Frequency of pain question C0009663 Condylomata acuminata HSDN C0700078 Deep tendon reflex decrease C1858391 Ataxia-telangiectasia-like disorder HPO C2203646 Jaundice C3150343 Hemolytic anemia, nonspherocytic, due to hexokinase deficiency HPO C4084768 Usual severity vomiting C0033289 Family relationship, professional HSDN C0030975 Disorders perception C0025312 Meningomyelocele HSDN C1963087 Constipation adverse event C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0018991 Paralysis one side of body C0001122 Acidosis HSDN C0030193 Sense of pain C0025521 Inborn errors of metabolism HSDN C2911647 Weight gain adverse event C0041230 Bovine trypanosomiases HSDN C0231528 Muscle pain generalized C1963138 Hypertension adverse event HSDN C0028738 Nystagmus C3539013 Aicardi-goutieres syndrome 6 MalaCards C0020672 Body temperature decreased C0022661 Kidney failure, chronic HSDN C0851578 Disorder sleep C0014550 Epilepsies, myoclonic HSDN C1384666 Decreased hearing C0021359 Infertility HSDN C0751295 Memory loss or impairment C3807295 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant MalaCards|UMLS C0030193 Sense of pain C0013124 Behavior drinking HSDN C4084775 Usual severity weight loss C3541306 Plasmodium measurement HSDN C0018681 Headache, cephalalgia C0031347 Pharyngeal neoplasms HSDN C4084773 Bothered by weight gain C2240374 Eosinophil count raised HSDN C4085210 Usual severity pain C0030353 Papilledema HSDN C4085210 Usual severity pain C0334082 Nevus, epidermal (disorder) OrphaNet C0242936 Center pain C0005747 Blepharospasm HSDN C0028961 Urine output decreased C0752166 Bardet-biedl syndrome HSDN C1963252 Tremor adverse event C0011854 Diabetes mellitus, insulin-dependent HSDN C0019825 Voice hoarseness C0152180 Accessory nerve diseases HSDN C0015469 Facial paralysis C0042035 Urination disorders HSDN C0015672 Decreased energy C0033918 Military psychology HSDN C0030554 Abnormal sensation C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0013720 Ehlers-danlos syndrome HSDN C4084775 Usual severity weight loss C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C0018681 Headache, cephalalgia C0043395 Yellow fever DiseaseOntology|OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C3280598 Short-rib thoracic dysplasia 5 with or without polydactyly MalaCards C3829611 Nausea frequency C1963107 Euphoria adverse event HSDN C0022107 Fussiness C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0017671 Glomus jugulare tumor HSDN C0035229 Respiratory function impaired C3150413 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 MalaCards|HPO C0034155 Thrombotic thrombocytopenic purpura C0001733 Afibrinogenemia HSDN C0030554 Abnormal sensation C0023827 Liposarcoma MalaCards C0020615 Hypoglycemia nos C1829703 Carnitine palmitoyl transferase 1a deficiency OrphaNet|HPO C2242996 Tingling C2911643 Encounter due to family history of osteoporosis HSDN C4085642 Level of joint stiffness C2931642 Benign symmetrical lipomatosis OrphaNet|HPO|MalaCards C4084776 Weight loss C1527336 Sjogren's syndrome HSDN C0427190 Ataxia, truncal C3150876 Congenital disorder of glycosylation, type iii MalaCards|HPO C0018834 Brash C4085311 Depression - recess HSDN C0043094 Weight gain C0007787 Transient ischemic attack HSDN C0010200 Cough symptom C0571941 Lisinopril allergy UMLS C0004134 Dyssynergia C0428953 Ecg infarction myocardial HSDN C3829611 Nausea frequency C0017181 Gastrointestinal hemorrhage HSDN C0018681 Headache, cephalalgia C0206663 Neuroectodermal tumor, primitive MalaCards C0015672 Decreased energy C0019360 Herpes zoster disease HSDN C0022568 Inflammation corneal C1848413 Trichothiodystrophy, type 1 HPO C4084769 Vomiting frequency C0037937 Spine injury HSDN C2036498 Stuttering characterized by repetition of 'uh' C0038506 Stuttering UMLS C0011991 Loose stools C0717360 Disease lyme vaccine HSDN C0013604 Edematous C0038557 Submandibular gland diseases HSDN C0413252 Hypothermia due to exposure C0013922 Embolism HSDN C0011991 Loose stools C0043395 Yellow fever OrphaNet|MalaCards C0013604 Edematous C0032227 Pleural effusion disorder HSDN C0020673 Hypothermia (central) (local) C0086543 Cataract nos HSDN C1963184 Nystagmus adverse event C2678262 Methylmalonic aciduria, cblh type, formerly HPO C4084776 Weight loss C0025289 Meningitis HSDN C1963249 Tinnitus adverse event C0038186 Reflex, startle HSDN C2024893 Cardiovascular surgery result: fatigue C0035222 Respiratory distress syndrome, adult HSDN C0018681 Headache, cephalalgia C0346303 Thyrotroph adenoma OrphaNet|MalaCards C0028961 Urine output decreased C0221752 Rbc urine HSDN C0036572 Convulsion C1864840 Combined oxidative phosphorylation deficiency 3 MalaCards|HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0162557 Liver failure, acute HSDN C0005745 Blepharoptosis C0265373 Fetal trimethadione syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0010074 Coronary vessel anomalies HSDN C0009806 Constipate C0019326 Ventral hernia HSDN C0522224 Palsied C0011334 Dental caries HSDN C0497247 Blood pressure elevation C0403555 Ochoa syndrome MalaCards|HPO C0039070 Collapse fleeting C0085380 Anxiety dental HSDN C0454644 Delayed language development C3554385 Congenital disorder of glycosylation, type iu MalaCards C0020450 Hyperemesis gravidarum C0041296 Tuberculosis HSDN C0007758 Cerebellar ataxia C0022758 Kap HSDN C0557874 Global developmental delay C1720864 Sulfatidosis, juvenile, austin type OrphaNet|HPO|MalaCards C0427055 Face weakness C2673677 Myopathy, early-onset, with fatal cardiomyopathy MalaCards|HPO|UMLS C4085317 Diarrhea frequency C0017185 Gastrointestinal neoplasms HSDN C0042963 Symptoms vomiting C0040156 Thyrotoxicosis HSDN C0000737 Abdomen pain C0019618 Histiocytosis HSDN C1963281 Vomiting adverse event C1999266 Depression adverse event HSDN C0013404 Respiratory difficulty C0206634 Liposarcoma, myxoid HSDN C2700617 Irritation - emotion C2931919 X-linked infantile spasm syndrome MalaCards C0042571 Vertigo subjective C0029888 Otitis media purulent HSDN C4085211 Pain distress question C0282612 Prostatic intraepithelial neoplasias HSDN C0018784 Deafness sensorineural C0042138 Uterine neoplasms HSDN C0349588 Stature short C0155338 Total ophthalmoplegia MalaCards C1963135 Hepatic necrosis adverse event C0345904 Malignant neoplasm of liver MalaCards C0036572 Convulsion C1850510 Sialidosis, type i OrphaNet|HPO C4084766 Vomiting C0026598 Movement perception HSDN C1549543 Administration method - pain C0022364 Jaw neoplasms HSDN C0018772 Deafness C0205711 Pelizaeus-merzbacher disease OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0030489 Paraproteinemias HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007279 Carotid body paraganglioma HSDN C1549543 Administration method - pain C0026780 Mumps HSDN C1069915 Vertigo C0001175 Acquired immunodeficiency syndrome HSDN C0004134 Dyssynergia C1834846 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 UMLS C0030486 Extremity paralysis, lower C0004352 Autistic disorder HSDN C4085210 Usual severity pain C0031347 Pharyngeal neoplasms HSDN C0031315 Phantom limb pain C1458155 Mammary neoplasms HSDN C0349588 Stature short C3888138 Monosomy x MalaCards C0013362 Dysarthrias C0017495 Gerstmann-straussler-scheinker disease MalaCards|HSDN|HPO C0007398 Catatonic C0030631 Aggressive passive personality HSDN C0022107 Fussiness C0795889 Allan-herndon-dudley syndrome (ahds) MalaCards|HPO C4084766 Vomiting C0376532 Epilepsy, rolandic HSDN C1963281 Vomiting adverse event C0085277 Munchausen by proxy syndrome HSDN C0026826 High muscle tone C1845102 Hyperekplexia and epilepsy MalaCards|HPO C0917816 Deficiency mental C1845408 Contiguous abcd1-dxs1375e deletion syndrome MalaCards|HPO C0023015 Language handicap C0004364 Autoimmune diseases HSDN C2945560 Hemolytic C0002895 Anemia, sickle cell MalaCards C0010520 Skin cyanosis C0024586 Malignant carcinoid syndrome HSDN C3539892 Pelvic pain in front C0037051 Behavior illness HSDN C4085210 Usual severity pain C0152177 Trigeminal neuropathy HSDN C1000483 Genus anemia C2673609 Epidermolysis bullosa inversa dystrophica MalaCards C0270327 Bed wetting C1857844 Williams-beuren region duplication syndrome MalaCards C0151686 Growth retardation C0268487 Tyrosine transaminase deficiency disease MalaCards|HPO C2984058 Have pain C0036982 Shock, hemorrhagic HSDN C0497247 Blood pressure elevation C2931468 Cystic hamartomata of lung and kidney OrphaNet|MalaCards C0039070 Collapse fleeting C0033578 Prostatic neoplasms HSDN C0018524 Hallucinate C3658321 Acceptance and commitment therapy HSDN C1069915 Vertigo C0032209 Platybasia HSDN C0917816 Deficiency mental C1621920 Intermediate maple syrup urine disease HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0026718 Mucormycosis HSDN C0018772 Deafness C1327918 Oculootoradial syndrome MalaCards|HPO C0026603 Motion sickness C0033968 Psychotherapeutic technique HSDN C0234378 Postural tremor C1836383 Spinocerebellar ataxia 27 HPO C1000483 Genus anemia C3551954 Coenzyme q10 deficiency, primary, 1 MalaCards C1963091 Diarrhea adverse event C0997768 Glaucoma HSDN C0018926 Emesis bloody C0032787 Postoperative complications HSDN C0004310 Auditory disorder process C0009240 Cognition HSDN C0518090 Frequency of pain question C0751795 Head injury penetrating HSDN C0033377 Caudal displacement C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C2315100 Pediatric failure to thrive C0341106 Eosinophilic esophagitis MalaCards C0015970 Fever unknown origin C0018916 Hemangioma HSDN C4085862 Bothered by nausea C1963064 Anxiety adverse event HSDN C0038002 Spleen enlargement C1850568 Nakajo syndrome MalaCards|HPO C0018681 Headache, cephalalgia C4039776 Migraine caused by estrogen contraceptive UMLS C0518090 Frequency of pain question C0023786 Mucopolysaccharidosis i HSDN C0011991 Loose stools C0206603 Circoviridae infection HSDN C0030552 Paralysis partial C0009373 Colonic diseases HSDN C3641756 Have diarrhea C0040948 Trichostrongyliasis HSDN C0030552 Paralysis partial C0004610 Bacteremia HSDN C0522224 Palsied C1547940 Specimen source codes - ulcer HSDN C3146279 Coma C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C0015468 Face pain C0010606 Adenoid cystic carcinoma HSDN C0012833 Dizzy C0267797 Acute hepatitis UMLS C0035229 Respiratory function impaired C2930957 Hantavirosis OrphaNet|MalaCards C0015672 Decreased energy C0279549 Philadelphia chromosome negative chronic myelogenous leukemia UMLS C1963071 Back pain adverse event C0031118 Peripheral nervous system neoplasms HSDN C0039070 Collapse fleeting C0040136 Thyroid neoplasm HSDN C0000727 Abdomen acute C0040558 Toxoplasmosis HSDN C4085222 Nausea C0085293 Hepatitis e MalaCards C0022346 Yellow skin C0206624 Hepatoblastoma MalaCards|UMLS C0427055 Face weakness C0026896 Myasthenia gravis MalaCards|UMLS C1963093 Dizziness adverse event C0011615 Dermatitis, atopic HSDN C0030193 Sense of pain C1963059 Adrenal insufficiency adverse event HSDN C4085210 Usual severity pain C0013449 Ear neoplasms HSDN C3641755 Have constipation C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C2984058 Have pain C0242659 Female homosexual HSDN C0005745 Blepharoptosis C3280766 Joubert syndrome 14 MalaCards C4084769 Vomiting frequency C0085277 Munchausen by proxy syndrome HSDN C0026838 Spasticity muscle C0752130 Spinal cord ischemia HSDN C1963184 Nystagmus adverse event C0796272 Brooks syndrome MalaCards C0014591 Bleeding nose C1848534 Vitamin k-dependent clotting factors, combined deficiency of, 1 MalaCards|HPO C0004604 Pain back C1868649 Panic disorder 1 HSDN C0020673 Hypothermia (central) (local) C3541306 Plasmodium measurement HSDN C0151686 Growth retardation C3495483 Amish brittle hair syndrome MalaCards C0242936 Center pain C0031039 Effusion pericardial HSDN C0013390 Cramps menstrual C0010674 Cystic fibrosis HSDN C0042798 Vision dim C0238045 Carotid artery-cavernous sinus fistula HSDN C1549543 Administration method - pain C0040761 Transposition of great vessels HSDN C0004310 Auditory disorder process C0007820 Cerebrovascular disorders HSDN C0004134 Dyssynergia C0034069 Pulmonary fibrosis HSDN C0518090 Frequency of pain question C0023492 Leukemia, t-cell HSDN C0522224 Palsied C2587212 Parturient paresis HSDN C4084802 Usual severity diarrhea C0026269 Mitral valve stenosis HSDN C0013144 Drowsy C1850055 Peho syndrome OrphaNet|HPO|MalaCards C0030554 Abnormal sensation C1457883 Aggressive reaction HSDN C0033377 Caudal displacement C0346303 Thyrotroph adenoma MalaCards C1557397 Adverse event associated with pain C3812171 Bradycardia by ecg finding HSDN C0427055 Face weakness C1852502 Craniometaphyseal dysplasia, autosomal dominant HPO C0033377 Caudal displacement C0003076 Aniridia OrphaNet C4085211 Pain distress question C0005396 Bile duct neoplasms HSDN C0151889 Reflexes tendon increased C0268496 Kramer syndrome OrphaNet|MalaCards C0728710 Pupil constriction observed C0034119 Punishment HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0031039 Effusion pericardial HSDN C0030554 Abnormal sensation C0027804 Fatigue neurosis HSDN C0234146 Absent reflex C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C0151786 Weakness muscle C1963067 Atrial fibrillation adverse event HSDN C1557397 Adverse event associated with pain C0038354 Stomach diseases HSDN C4084727 Cough frequency C0036421 Systemic scleroderma OrphaNet|HSDN|MalaCards C1963093 Dizziness adverse event C0031090 Periodontal diseases HSDN C0003113 Anomia C0085084 Motor neuron disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0022660 Kidney failure, acute HSDN C0036572 Convulsion C0085207 Gestational diabetes HSDN C0030552 Paralysis partial C0155338 Total ophthalmoplegia MalaCards C2237041 Shox gene with short stature C3150215 Chromosome 6q24-q25 deletion syndrome MalaCards C2911645 Weight loss adverse event C0346407 Pancreatic polypeptide-oma MalaCards C4084802 Usual severity diarrhea C0242339 Dyslipidemias HSDN C3898969 Have been vomiting C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C1963087 Constipation adverse event C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C1963137 Hydrocephalus adverse event C1851101 Laurin-sandrow syndrome, segmental MalaCards C0013604 Edematous C0009766 Allergic conjunctivitis HSDN C0040264 Ear ringing sound C2931205 Usher syndrome, type 1a MalaCards C4085211 Pain distress question C0236969 Substance-related disorders HSDN C0018784 Deafness sensorineural C0265253 Stickler syndrome (disorder) OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C3495559 Juvenile arthritis HSDN C0004134 Dyssynergia C2827407 Infectious otitis media HSDN C4085661 Usual severity nausea C0205788 Histiocytoid hemangioma HSDN C0003126 Smell loss C4023767 Partial anosmia UMLS C0030193 Sense of pain C0458220 Nervus intermedius neuralgia UMLS C0020578 Hyperventilate C0010054 Coronary arteriosclerosis HSDN C0019079 Bloody sputum C3887645 Job syndrome HSDN C0751495 Seizure focal C0751383 Juvenile neuronal ceroid lipofuscinosis OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0030977 Perceptual masking HSDN C0013404 Respiratory difficulty C1968593 Respiratory distress syndrome in premature infants UMLS C4085210 Usual severity pain C0013295 Duodenal ulcer HSDN C0242936 Center pain C0013533 Echovirus infections HSDN C0242936 Center pain C0029944 Drug overdose HSDN C4085661 Usual severity nausea C0013299 Duodenogastric reflux HSDN C0349588 Stature short C0008626 Congenital chromosomal disease MalaCards C2013427 Oral cavity symptoms C0006430 Burning mouth syndrome UMLS C4084768 Usual severity vomiting C0039980 Chest injury HSDN C0085636 Light sensitivity C0314719 Dryness of eye HSDN C0917816 Deficiency mental C1846790 Joubert syndrome 4 (disorder) MalaCards C0042571 Vertigo subjective C0038354 Stomach diseases HSDN C4084773 Bothered by weight gain C0041956 Ureteral obstruction HSDN C0036572 Convulsion C2931005 Congenital disorder of glycosylation type 1k OrphaNet|HPO|MalaCards C0349588 Stature short C1835819 Pituitary anomalies with holoprosencephaly-like features (disorder) HPO C0424755 Fever symptoms C0018018 Goat disease HSDN C0018772 Deafness C0265376 Fetal methyl mercury syndrome OrphaNet C0234146 Absent reflex C1836607 Myotilinopathy MalaCards|HPO C3146279 Coma C0012739 Disseminated intravascular coagulation HSDN C2984058 Have pain C0035613 Rift valley fever HSDN C0042963 Symptoms vomiting C0026850 Muscular dystrophy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041960 Ureterocele HSDN C1557397 Adverse event associated with pain C0242216 Biliary calculi HSDN C1963071 Back pain adverse event C2963140 Arteriovenous fistula in use with two needles HSDN C0042963 Symptoms vomiting C1999266 Depression adverse event HSDN C0009421 Comatose C1563215 Powassan encephalitis virus infection MalaCards C1000483 Genus anemia C0038325 Stevens-johnson syndrome HPO C0036572 Convulsion C0311334 Generalized convulsive seizure UMLS C0007859 Pain neck C0810353 Other back pain and disorders UMLS C0518090 Frequency of pain question C0085426 Gram-positive bacterial infections HSDN C0020672 Body temperature decreased C0007787 Transient ischemic attack HSDN C0030193 Sense of pain C0038833 Superior vena cava syndrome HSDN C2096293 Ent surgical result ear vertigo C0029456 Osteoporosis HSDN C0037316 Not enough sleeping C0007273 Carotid artery diseases HSDN C1443924 Severe diarrhea C0002831 Ancylostomiasis MalaCards C1963274 Vasculitis adverse event C0085655 Polymyositis MalaCards C0013390 Cramps menstrual C0014173 Endometrial hyperplasia HSDN C3641756 Have diarrhea C0002874 Aplastic anemia HSDN C2984058 Have pain C0006105 Brain abscess HSDN C2073625 X-ray of chest: pleural effusion C0085083 Ovarian hyperstimulation syndrome OrphaNet|HPO|MalaCards C1384666 Decreased hearing C1855900 Hypertrichosis, congenital generalized MalaCards C0014591 Bleeding nose C1839163 Thrombocytopenia 1 (disorder) HPO C0043352 Absent salivary secretion C0162359 Christ-siemens-touraine syndrome OrphaNet|MalaCards C0023014 Developmental disorder language C0016563 Form perception HSDN C3541349 Syncope C0024305 Lymphoma, non-hodgkin HSDN C0011991 Loose stools C0029883 Otitis media with effusion HSDN C2025995 Cellulitis C0406645 Amyopathic dermatomyositis MalaCards C0018834 Brash C1275808 Congenital central hypoventilation MalaCards C1963170 Hypothermia adverse event C0749420 Thyroid agenesis HPO C0002170 Alopecia disorders C0549567 Pigmentation disorders MalaCards C2921132 Full incontinence of feces C4237327 Other specified elimination disorder, with fecal symptoms UMLS C0030552 Paralysis partial C0017923 Glycogen storage disease type iv MalaCards|HPO C1963091 Diarrhea adverse event C0010072 Coronary thrombosis HSDN C0020578 Hyperventilate C0024433 Macrostomia HSDN C0013395 Indigestion C2945560 Hemolytic HSDN C2984057 Have nausea C1260386 Glucocorticoid-remediable aldosteronism HPO C0003079 Pupillary inequality C0027092 Myopia HSDN C0009398 Color vision defects C0017181 Gastrointestinal hemorrhage HSDN C0242936 Center pain C0032269 Pneumococcal infections HSDN C2024893 Cardiovascular surgery result: fatigue C0042134 Uterine hemorrhage HSDN C0042024 Urine incontinence C0031117 Peripheral neuropathy HSDN C0235242 Syncope exertional C0340854 Situational syncope UMLS C3463815 Feel fatigue C1704421 Skin pigmentation disorder HSDN C0013362 Dysarthrias C0002949 Aneurysm, dissecting HSDN C1963252 Tremor adverse event C2677326 Epileptic encephalopathy, early infantile, 4 MalaCards|HPO C3539893 Pelvic pain occurs with intercourse C0037929 Spinal cord injuries HSDN C0034150 Skin purpura C0001418 Adenocarcinoma HSDN C0020672 Body temperature decreased C0030567 Parkinson disease HSDN C4020887 Photodysphoria C0265966 Hereditary benign intraepithelial dyskeratosis MalaCards C4084802 Usual severity diarrhea C0428977 Bradycardia HSDN C2911645 Weight loss adverse event C1261473 Sarcoma HSDN C0242936 Center pain C0030521 Parathyroid neoplasms HSDN C0018834 Brash C0009946 Conversion disorder HSDN C0518090 Frequency of pain question C0311468 Increased bilirubin level (finding) HSDN C0034150 Skin purpura C1579931 Depressed - symptom HSDN C0041657 Consciousness loss C0035204 Respiration disorders HSDN C0043094 Weight gain C0015579 Family characteristics HSDN C0426579 Anorexia symptom C0039006 Swine--diseases HSDN C4084727 Cough frequency C0010054 Coronary arteriosclerosis HSDN C2984058 Have pain C0014059 Encephalomyelitis, acute disseminated HSDN C0024031 Back pain lower back C0011603 Dermatitis HSDN C0151686 Growth retardation C0795865 Chromosome 17, trisomy 17p OrphaNet C0234146 Absent reflex C1859228 Cerebrohepatorenal syndrome, variant types HPO C0037316 Not enough sleeping C0342257 Complications of diabetes mellitus HSDN C4084766 Vomiting C0524812 Intracranial hypotension HSDN C0003862 Pain joint C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C1549543 Administration method - pain C0026654 Moyamoya disease HSDN C4084769 Vomiting frequency C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C0003910 Articulation disorder C4085311 Depression - recess HSDN C4084769 Vomiting frequency C0019699 Hiv seropositivity HSDN C3463815 Feel fatigue C0002989 Epithelioid hemangioma of skin HSDN C0018775 Hearing loss bilateral C0041409 Turner syndrome, male HSDN C0020578 Hyperventilate C0011849 Diabetes mellitus HSDN C4084774 Have weight loss C0010414 Infection by cryptococcus neoformans HSDN C1384666 Decreased hearing C0037397 Behavior social HSDN C0232461 Increased appetite C1867858 Prader-willi syndrome chromosome region HPO C0013404 Respiratory difficulty C0010674 Cystic fibrosis HSDN C0027066 Myoclonic jerking C0018802 Congestive heart failure HSDN C0150055 Pain chronic C0085413 Polycystic kidney, autosomal dominant HSDN C3887784 Decreased urine output C0027726 Nephrotic syndrome HSDN C0042963 Symptoms vomiting C0003496 Aortic rupture HSDN C4084774 Have weight loss C2911643 Encounter due to family history of osteoporosis HSDN C0332563 Papulae C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C2984058 Have pain C0026948 Mycosis fungoides HSDN C0007758 Cerebellar ataxia C0008521 Choroid diseases HSDN C0042024 Urine incontinence C0035243 Respiratory tract infections HSDN C0015300 Ocular proptosis C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards|HPO C2984058 Have pain C0206062 Lung diseases, interstitial HSDN C0020538 Hbp C0342443 Adrenal cushing's syndrome MalaCards C0026821 Cramp C0042035 Urination disorders HSDN C4085210 Usual severity pain C1963148 Iron overload adverse event HSDN C0000737 Abdomen pain C0013080 Down syndrome HSDN C3274924 Have been coughing C0037051 Behavior illness HSDN C1961131 Cough adverse event C0152938 Secondary pneumonic plague DiseaseOntology|MalaCards C3665386 Abnormal vision C0019562 Von hippel-lindau syndrome MalaCards|HPO C0004134 Dyssynergia C0039006 Swine--diseases HSDN C4084774 Have weight loss C0085423 Gram-negative bacterial infections HSDN C1962972 Proteinuria adverse event C0032227 Pleural effusion disorder HSDN C4084768 Usual severity vomiting C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C2315100 Pediatric failure to thrive C4014954 Neutropenia, severe congenital, 6, autosomal recessive MalaCards C1384666 Decreased hearing C0032371 Poliomyelitis HSDN C1549543 Administration method - pain C0237104 Spirituality HSDN C0039870 Leanness C0520679 Sleep apnea, obstructive HSDN C4085317 Diarrhea frequency C0275148 Poisoning of animal by plant HSDN C2024893 Cardiovascular surgery result: fatigue C0018824 Heart valve disease HSDN C0018681 Headache, cephalalgia C0040456 Tooth impaction HSDN C0030193 Sense of pain C0007860 Uterine cervicitis HSDN C0027796 Neuralgias C0023890 Liver cirrhosis HSDN C0426579 Anorexia symptom C0677614 Encounter due to convalescence HSDN C2984058 Have pain C1963215 Pneumothorax adverse event HSDN C3539020 Pelvic pain decreasing in frequency C1552262 Nurse practitioner - family HSDN C0008031 Pain chest C0004364 Autoimmune diseases HSDN C0015300 Ocular proptosis C0796202 Wittwer syndrome MalaCards C0004134 Dyssynergia C0022116 Ischemia HSDN C4084788 Have dizziness C0155490 Middle ear cholesteatoma HSDN C2919142 Short stature adverse event C1856871 Aarskog-like syndrome OrphaNet|MalaCards C0036396 Sciatica C2102996 Disorders of peripheral nerve, neuromuscular junction and muscle UMLS C0151786 Weakness muscle C0004275 Attitude health HSDN C0036572 Convulsion C0034734 Raynaud disease HSDN C2096293 Ent surgical result ear vertigo C0242342 Sheehan syndrome MalaCards C1963091 Diarrhea adverse event C0023448 Lymphoid leukemia HSDN C4085211 Pain distress question C0027707 Nephritis, interstitial HSDN C3665492 Pigmentations C0238451 Teratoma of testis MalaCards C3274924 Have been coughing C0035078 Kidney failure HSDN C4085211 Pain distress question C0311468 Increased bilirubin level (finding) HSDN C4084769 Vomiting frequency C0001118 Acid base imbalance HSDN C0424755 Fever symptoms C1762616 Meningioma, benign, no icd-o subtype HSDN C0018784 Deafness sensorineural C1704436 Peripheral arterial diseases HSDN C4084784 Diarrhea C0029182 Orbit (eye disorders) HSDN C0349588 Stature short C1135161 Stage 4s neuroblastoma MalaCards C0013404 Respiratory difficulty C0242875 Ventricular septal rupture HSDN C0494475 Seizure generalized tonic clonic C3809278 Epileptic encephalopathy, childhood-onset MalaCards C0518090 Frequency of pain question C0206754 Neuroendocrine tumors HSDN C0020673 Hypothermia (central) (local) C0403447 Chronic kidney insufficiency HSDN C0017181 Gastrointestinal bleed C1852456 Cryoglobulinemia, familial mixed MalaCards C0042024 Urine incontinence C0031149 Peritoneal neoplasms HSDN C0404484 Chronic female pelvic pain C1298685 Chronic pain syndrome UMLS C1557397 Adverse event associated with pain C0014461 Granuloma eosinophilic HSDN C0221263 Cafe au lait spot C1302282 Chromaffin cell neoplasm MalaCards C0917816 Deficiency mental C1321551 Shprintzen-goldberg syndrome HPO C0015300 Ocular proptosis C0019618 Histiocytosis MalaCards C0002963 Angina variant C0002064 Alkalosis, respiratory HSDN C2127524 Atrophy of both hands C0333641 Atrophic UMLS C3463815 Feel fatigue C0206138 Crest syndrome MalaCards C0349588 Stature short C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0232491 Abdomen discomfort chronic C0012819 Diverticular disease of colon UMLS C0030193 Sense of pain C0041107 Trisomy HSDN C0000727 Abdomen acute C0008311 Cholangitis HSDN C0007166 Cardiac output decreased C0002895 Anemia, sickle cell HSDN C0016382 Cutaneous vascular engorgement C0085106 Familial benign pemphigus OrphaNet|HPO C0019079 Bloody sputum C0007820 Cerebrovascular disorders HSDN C0030193 Sense of pain C0236964 Attention deficit and disruptive behavior disorders HSDN C2237041 Shox gene with short stature C2931187 Nephropathic cystinosis MalaCards C0013395 Indigestion C0023903 Liver neoplasms HSDN C4085317 Diarrhea frequency C0024116 Lung diseases, fungal HSDN C0020580 Decreased sensation C0029423 Cartilaginous exostosis HSDN C1963071 Back pain adverse event C0024636 Malocclusion HSDN C0019209 Large liver C0086652 Mucopolysaccharidosis type ivb HPO C0003811 Cardiac rhythm disturbance C2678055 Myopathy, x-linked, with postural muscle atrophy (disorder) MalaCards|HPO C1963091 Diarrhea adverse event C0023473 Myeloid leukemia, chronic HSDN C4084788 Have dizziness C0011265 Presenile dementia HSDN C0000731 Abdomen distention C0268186 Congenital glucose-galactose malabsorption MalaCards|HPO C0002962 Angina C0002884 Hypochromic anemia HSDN C4084724 Usual severity constipation C0717360 Disease lyme vaccine HSDN C4084768 Usual severity vomiting C0018944 Hematoma HSDN C2187990 Unable to perform sex C0162309 Adrenoleukodystrophy MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0017924 Glycogen storage disease type v HSDN C0034933 Abnormal reflexes C0016412 Folic acid deficiency HSDN C0018834 Brash C1279945 Acute interstitial pneumonia MalaCards C1549543 Administration method - pain C0035457 Rhinitis, allergic, perennial HSDN C4084773 Bothered by weight gain C0007820 Cerebrovascular disorders HSDN C0020673 Hypothermia (central) (local) C0018671 Head and neck neoplasms HSDN C0024031 Back pain lower back C0034885 Rectal neoplasms HSDN C4084766 Vomiting C0012644 Animal disease models HSDN C0028738 Nystagmus C0087012 Ataxia, spinocerebellar MalaCards C3665347 Vision impaired C1863389 Apert-crouzon disease MalaCards C4084767 Bothered by vomiting C0031347 Pharyngeal neoplasms HSDN C0423698 Pain in amputated limb C0031315 Phantom limb pain UMLS C0857305 Thrombocytopenia purpura C0003850 Arteriosclerosis HSDN C4085211 Pain distress question C0024301 Lymphoma, follicular HSDN C4084775 Usual severity weight loss C0021361 Female infertility HSDN C1384666 Decreased hearing C1868684 Ear, patella, short stature syndrome MalaCards|HPO C0349588 Stature short C2931680 Camptodactyly syndrome guadalajara type 2 OrphaNet|MalaCards C0030193 Sense of pain C0010678 Cysticercosis HSDN C0518090 Frequency of pain question C0027707 Nephritis, interstitial HSDN C0000737 Abdomen pain C3273114 Gallbladder adenocarcinoma, gastric foveolar type UMLS C1963091 Diarrhea adverse event C0029463 Osteosarcoma HSDN C0020438 Hypercalciuria C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0030193 Sense of pain C0270327 Bedwetting HSDN C0009460 Communication impairment C0392347 Hope HSDN C0018681 Headache, cephalalgia C0013182 Drug allergy HSDN C1527344 Dysphonia C0334419 Pheochromocytoma, malignant MalaCards C0036572 Convulsion C1335658 Radiation-induced intracranial meningioma UMLS C0349588 Stature short C0796206 Atkin syndrome OrphaNet|MalaCards C0010200 Cough symptom C0004114 Astrocytoma HSDN C0013404 Respiratory difficulty C0242184 Hypoxia UMLS C0024031 Back pain lower back C0036974 Shock HSDN C0344428 Ventricular tachycardia by ecg finding C2677794 Stress-induced polymorphic ventricular tachycardia MalaCards|HPO C0398650 Idiopathic thrombocytopenia purpura C0026946 Mycoses HSDN C0013604 Edematous C0020437 Hypercalcemia HSDN C2096293 Ent surgical result ear vertigo C0023448 Lymphoid leukemia HSDN C0041834 Erythematous condition C1836284 Epidermolysis bullosa simplex with migratory circinate erythema OrphaNet|HPO C0018784 Deafness sensorineural C0051981 Anti-leprosy vaccine HSDN C0015672 Decreased energy C0021568 Bites insect stings HSDN C0041657 Consciousness loss C0428977 Bradycardia HSDN C0013428 Painful urination C0152276 Granulocytic sarcoma HSDN C4084769 Vomiting frequency C0025222 Melena HSDN C0037317 Sleep disturbance C0006287 Bronchopulmonary dysplasia MalaCards C0012569 Double vision C0041327 Tuberculosis, pulmonary HSDN C0018777 Deafness, conductive C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0038220 Status epilepticus HSDN C0039070 Collapse fleeting C0453996 Tobacco smoking HSDN C0000737 Abdomen pain C0282207 Cronkhite-canada syndrome OrphaNet|UMLS|MalaCards C0022568 Inflammation corneal C0022283 Incontinentia pigmenti achromians MalaCards|HPO C0026884 Muteness C4041080 Neurocognitive disorders HSDN C0038506 Stutter C0751739 Basal ganglia cerebrovascular disease HSDN C0034150 Skin purpura C0003706 Arachnodactyly HSDN C0349588 Stature short C0342345 Hypoparathyroidism - autosomal dominant MalaCards C4084768 Usual severity vomiting C1963266 Uveitis adverse event HSDN C0152116 Torticollis spasmodic C1836756 Arthrogryposis, distal, type 4 (disorder) MalaCards C4085211 Pain distress question C0037997 Splenic diseases HSDN C0518090 Frequency of pain question C0004030 Aspergillosis HSDN C3641756 Have diarrhea C0003184 Anthropology HSDN C0232466 Feeding difficulty C2931246 Chromosome 17, trisomy 17p11 2 MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C4085549 Dizziness C1522133 High cholesterol level HSDN C2911645 Weight loss adverse event C0398623 Thrombophilia HSDN C0024031 Back pain lower back C0026850 Muscular dystrophy HSDN C4084773 Bothered by weight gain C1963134 Hemorrhoids adverse event HSDN C0234132 Pyramidal sign C0023788 Whipple disease MalaCards C0036572 Convulsion C0002063 Alkalosis HSDN C0522224 Palsied C0007795 Diffuse cerebral sclerosis of schilder MalaCards|HSDN C2237041 Shox gene with short stature C0282525 Adrenoleukodystrophy, neonatal OrphaNet|HPO|MalaCards C0587047 Mass of trunk C0266416 Congenital; cyst, vulva UMLS C0587246 Extremity weakness C2750536 Nemaline myopathy 3, with intranuclear rods HPO C2233556 Epistaxis stops with nasal packing C0014591 Epistaxis UMLS C4084776 Weight loss C0033860 Psoriasis HSDN C0023014 Developmental disorder language C1000483 Genus anemia HSDN C0030486 Extremity paralysis, lower C0747533 Peroneal neuropathy HSDN C0085593 Chill C0238909 Cat scratch MalaCards C0042571 Vertigo subjective C0025427 Mercury poisoning HSDN C0018524 Hallucinate C0520679 Sleep apnea, obstructive HSDN C0239819 Hand edema C0239340 Edema of lower extremity UMLS C0039870 Leanness C0020517 Hypersensitivity HSDN C3887638 Failure to thrive in infant C3665624 Serum calcium below normal HSDN C0026826 High muscle tone C0265210 Weaver syndrome OrphaNet|HPO|MalaCards C0349588 Stature short C3279807 Ced3 MalaCards C0232462 Appetite decrease C0206743 Rhabdoid tumor OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C0007820 Cerebrovascular disorders HSDN C0028738 Nystagmus C0268407 Senile cardiac amyloidosis MalaCards C0039070 Collapse fleeting C0026785 Munchhausen syndrome HSDN C3539890 Pelvic pain causes awakening at night C0001624 Adrenal gland neoplasms HSDN C0030193 Sense of pain C2240374 Eosinophil count raised HSDN C0018772 Deafness C2936631 Complaint, subjective health HSDN C0020305 Fetal edema C0007001 Carbohydrate metabolism, inborn errors HSDN C0476273 Distress respiratory C1842462 Campomelic dysplasia with autosomal sex reversal HPO C0026826 High muscle tone C1837206 Cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly HPO C0036572 Convulsion C1860518 Vasculopathy, retinal, with cerebral leukodystrophy OrphaNet|UMLS|HPO|MalaCards C0023530 Leukopenia C0024788 Green monkey virus disease OrphaNet|MalaCards C1971624 Appetite absent C0017689 Glucagonoma OrphaNet|MalaCards C3463815 Feel fatigue C2240378 Cleft palate on exam HSDN C3541349 Syncope C0018767 Auditory sense HSDN C4085210 Usual severity pain C0027626 Neoplasm invasiveness HSDN C1565249 Limitation, mobility C0010054 Coronary arteriosclerosis HSDN C3815497 Cough C0006118 Brain neoplasms HSDN C4020887 Photodysphoria C1858562 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 MalaCards|HPO C1963093 Dizziness adverse event C0001807 Aggressive behavior HSDN C4084726 Distress cough C4015016 Ciliary dyskinesia, primary, 30 MalaCards C3641755 Have constipation C0038661 Suicide HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0037072 Diseases sigmoid HSDN C2919142 Short stature adverse event C0005956 Bone marrow diseases MalaCards C4084724 Usual severity constipation C0019557 Hip fx HSDN C4084773 Bothered by weight gain C0020507 Hyperplasia HSDN C0007758 Cerebellar ataxia C1962963 Osteoporosis adverse event HSDN C0587047 Mass of trunk C0266236 Cysts peritoneal UMLS C0019079 Bloody sputum C1962958 Hematoma adverse event HSDN C3898969 Have been vomiting C0037929 Spinal cord injuries HSDN C1549543 Administration method - pain C0031094 Periodontal pocket HSDN C1963093 Dizziness adverse event C0038579 Substance abuse, intravenous HSDN C0042963 Symptoms vomiting C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0973461 Dysphasia C2363129 Benign rolandic epilepsy MalaCards C3539022 Pelvic pain decreasing in severity C0009404 Colorectal neoplasms HSDN C1557397 Adverse event associated with pain C0206695 Carcinoma, neuroendocrine HSDN C1384666 Decreased hearing C0086649 Mps iii c HPO C0019521 Hiccoughs C1619738 Immune reconstitution inflammatory syndrome HSDN C0013404 Respiratory difficulty C0026267 Mitral valve prolapse syndrome HSDN C3641756 Have diarrhea C0005686 Urinary bladder diseases HSDN C2242996 Tingling C1578691 Congenital myxedema MalaCards C0009806 Constipate C0221210 Congenital malrotation of intestine UMLS C3898969 Have been vomiting C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency HPO C1961131 Cough adverse event C0024305 Lymphoma, non-hodgkin HSDN C0030193 Sense of pain C0029443 Osteomyelitis HSDN C0013604 Edematous C0030920 Peptic ulcer HSDN C0013362 Dysarthrias C0268262 Metachromatic leukodystrophy due to saposin b deficiency HPO C4084776 Weight loss C0001122 Acidosis HSDN C0018808 Murmur C0011570 Mental depression HSDN C3541349 Syncope C1550639 Specimen type - fistula HSDN C2073625 X-ray of chest: pleural effusion C0566602 Primary sclerosing cholangitis MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C1547046 Kind of quantity - taste HSDN C0848203 Male pelvic pain C0024141 Lupus erythematosus, systemic HSDN C0023012 Delay language C1412750 Bbs5 gene HPO C0240735 Personality change C1843257 Cataract, congenital, with mental impairment and dentate gyrus atrophy UMLS C4084788 Have dizziness C0003125 Anorexia nervosa HSDN C3887873 Hearing loss C1857663 Yunis varon syndrome MalaCards C4084769 Vomiting frequency C0024523 Malabsorption syndrome MalaCards|HSDN C0018808 Murmur C0043202 Wolff-parkinson-white syndrome HSDN C4085222 Nausea C0034088 Pulmonary valve insufficiency HSDN C4085210 Usual severity pain C2919115 Encounter due to bereavement HSDN C4085317 Diarrhea frequency C0302280 Adrenogenital syndrome HSDN C0030554 Abnormal sensation C0028879 Odontogenic cysts HSDN C0917816 Deficiency mental C2931141 Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency MalaCards|HPO C0036572 Convulsion C0234540 Convulsions uraemic UMLS C1963093 Dizziness adverse event C0022876 Premature obstetric labor HSDN C4085317 Diarrhea frequency C0012819 Diverticular disease of colon HSDN C0018784 Deafness sensorineural C0520946 Emotional hypersensitivity HSDN C1557397 Adverse event associated with pain C0005716 Blastomycosis HSDN C0344232 Blurred vision C2939149 Amyloid of cornea MalaCards C1963091 Diarrhea adverse event C1963137 Hydrocephalus adverse event HSDN C0860603 Anxiety symptom C2931205 Usher syndrome, type 1a MalaCards C4085210 Usual severity pain C0027645 Neoplasm seeding HSDN C4084726 Distress cough C3541994 Drug hypersensitivity syndrome MalaCards C0004134 Dyssynergia C0028077 Night blindness HSDN C2911645 Weight loss adverse event C0011875 Diabetic angiopathies HSDN C0030196 Limb pain C4023164 Abnormality of skeletal physiology UMLS C3274924 Have been coughing C0003504 Aortic valve insufficiency HSDN C1963091 Diarrhea adverse event C0016085 Filariasis HSDN C3463815 Feel fatigue C0023891 Liver cirrhosis, alcoholic HSDN C0000737 Abdomen pain C0524910 Hepatitis c, chronic MalaCards|HSDN C1963281 Vomiting adverse event C0026636 Mouth diseases HSDN C2984058 Have pain C0042636 Vibrio infection HSDN C4085317 Diarrhea frequency C0032708 Disorders of porphyrin metabolism OrphaNet|HSDN|MalaCards C0000737 Abdomen pain C0886483 Childhood malignant ovarian germ cell tumor UMLS C4084768 Usual severity vomiting C0023066 Laryngismus HSDN C0157536 Childbed fever C0405277 Puerperal pyrexia of unknown origin - delivered with postnatal complication UMLS C0013421 Dystonia C1843015 Alzheimer disease, familial, 3, with spastic paraparesis and apraxia HPO C4085210 Usual severity pain C0036917 Sexually transmitted diseases, bacterial HSDN C1963063 Anorexia adverse event C0017563 Gingival diseases HSDN C0033774 Skin pruritus C1275114 Epidermolysis bullosa pruriginosa OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0856761 Budd-chiari syndrome HSDN C2024893 Cardiovascular surgery result: fatigue C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0151889 Reflexes tendon increased C0520719 Spinopontine atrophy MalaCards C4084769 Vomiting frequency C0014457 Eosinophilia HSDN C1963065 Apnea adverse event C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C4085661 Usual severity nausea C0006147 Breast fed HSDN C4085661 Usual severity nausea C0024636 Malocclusion HSDN C0024032 Birth weight subnormal C1868684 Ear, patella, short stature syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0042345 Varicosity HSDN C1549543 Administration method - pain C0022602 Actinic keratosis HSDN C4084776 Weight loss C0005586 Bipolar disorder HSDN C0232466 Feeding difficulty C0432364 Accutane dysmorphic syndrome MalaCards C2315100 Pediatric failure to thrive C0022595 Keratosis follicularis HSDN C0026821 Cramp C0007137 Squamous cell carcinoma HSDN C0010520 Skin cyanosis C1955864 Cardiac sinus arrest HSDN C1962972 Proteinuria adverse event C0001580 Adolescent behavior HSDN C0003467 Angst C0085292 Stiff-person syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0031212 Personality disorders HSDN C0030193 Sense of pain C0030783 Pellagra HSDN C0030552 Paralysis partial C0018920 Hemangioma, cavernous HSDN C0005745 Blepharoptosis C4015141 Mental retardation, autosomal dominant 29 MalaCards C0009676 Confusion state C0302148 Blood clot HSDN C4085211 Pain distress question C2021655 Transvaginal ultrasound: anencephaly of fetus HSDN C0042940 Disorder of voice C0344315 Depressed mood HSDN C0035078 Failure kidney C3495490 Acrorenal syndrome OrphaNet|MalaCards C0042024 Urine incontinence C1963064 Anxiety adverse event HSDN C0085636 Light sensitivity C1848411 Xeroderma pigmentosum, complementation group e HPO C0015469 Facial paralysis C0032372 Poliomyelitis, anterior, acute HSDN C1557397 Adverse event associated with pain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C4042891 Sleep wake disorders C0013990 Pathological accumulation of air in tissues HSDN C0030552 Paralysis partial C0393571 Multiple system atrophy HSDN C0030975 Disorders perception C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C1557397 Adverse event associated with pain C0085404 Poems syndrome MalaCards|HSDN C0018784 Deafness sensorineural C0001807 Aggressive behavior HSDN C1963090 Dehydration adverse event C0343068 Familial cold urticaria MalaCards|HPO C1963154 Renal failure adverse event C0268643 Cystinuria type 1 MalaCards C0008031 Pain chest C0005940 Bone diseases HSDN C0241210 Speaking delay C0282512 Landau-kleffner syndrome MalaCards|HPO C0004310 Auditory disorder process C0175754 Agenesis of corpus callosum HSDN C0042928 Paralysis vocal cord C0920350 Autoimmune thyroiditis HSDN C4085210 Usual severity pain C0358297 Anthrax vaccines HSDN C1557397 Adverse event associated with pain C1258104 Diffuse scleroderma HSDN C0043094 Weight gain C0700208 Acquired scoliosis HSDN C0547004 Regular intermenstrual bleeding C0019080 Hemorrhage UMLS C0026821 Cramp C0037933 Spinal diseases HSDN C0221752 Rbc urine C1861848 Paragangliomas 4 MalaCards C0027796 Neuralgias C0037650 Somatoform disorder HSDN C0241165 Skin thickening C2745948 Hyalinosis, systemic MalaCards C0015676 Mental fatigue C0016053 Fibromyalgia HSDN C0004310 Auditory disorder process C0752308 Hypoxia-ischemia, brain HSDN C0002962 Angina C1963090 Dehydration adverse event HSDN C1963091 Diarrhea adverse event C0409959 Osteoarthritis, knee HSDN C0684343 Pseudophakia C0025202 Melanoma HSDN C3146279 Coma C0003864 Arthritis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0035956 Rupture spontaneous HSDN C0030486 Extremity paralysis, lower C0027809 Neurilemmoma HSDN C0015672 Decreased energy C0038379 Eye deviation HSDN C4084727 Cough frequency C0021818 Intervertebral disk displacement HSDN C0242670 Chronic vegetative state C0029456 Osteoporosis HSDN C4085549 Dizziness C0027804 Fatigue neurosis HSDN C0010200 Cough symptom C0742343 Acute chest syndrome DiseaseOntology|HSDN|MalaCards C2921140 Frontal lobe and executive function deficit C0154725 Oth disorder nervous system UMLS C0018784 Deafness sensorineural C0023176 Lead poisoning HSDN C0019209 Large liver C3553947 Peroxisome biogenesis disorder 6a (zellweger) MalaCards C0004941 Behavioral symptoms C1837475 Insulin-like growth factor i deficiency OrphaNet C0151311 Cranial nerve palsy C0393814 Hereditary liability to pressure palsies HPO C0011168 Disorder deglutition C0752125 Spinocerebellar ataxia type 7 MalaCards|HPO C4084726 Distress cough C0007820 Cerebrovascular disorders HSDN C4084774 Have weight loss C0008728 Churg-strauss syndrome OrphaNet|MalaCards C4085211 Pain distress question C0856761 Budd-chiari syndrome HSDN C0233844 Awkwardness C4015710 Tenorio syndrome MalaCards|UMLS C4085642 Level of joint stiffness C0265313 Weill-marchesani syndrome HPO C0424755 Fever symptoms C0039145 Syringomyelia and syringobulbia HSDN C3539893 Pelvic pain occurs with intercourse C0038941 Incisional infection HSDN C3829611 Nausea frequency C0037939 Spinal neoplasms HSDN C0030552 Paralysis partial C0004153 Atherosclerosis HSDN C0013456 Pain ear C1336537 Supratentorial meningioma MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0041956 Ureteral obstruction HSDN C4085317 Diarrhea frequency C0018188 Granuloma HSDN C0424755 Fever symptoms C0035042 Psychology and religion HSDN C0011991 Loose stools C0032310 Pneumonia, viral HSDN C0497406 Over weight C0014859 Esophageal neoplasms HSDN C0242936 Center pain C0011848 Diabetes insipidus HSDN C0004604 Pain back C0027794 Neural tube defects HSDN C0008031 Pain chest C0042514 Tachycardia, ventricular HSDN|UMLS C1963252 Tremor adverse event C0040409 Tongue diseases HSDN C0018777 Deafness, conductive C0004903 Beckwith-wiedemann syndrome HSDN C4084802 Usual severity diarrhea C0020635 Hypopituitarism HSDN C4084727 Cough frequency C0006434 Burn injury HSDN C0242936 Center pain C0011608 Dermatitis herpetiformis HSDN C0011991 Loose stools C1000587 Pemphigus HSDN C0018784 Deafness sensorineural C1547044 Kind of quantity - smell HSDN C0241210 Speaking delay C0796250 Partington x-linked mental retardation syndrome HPO C0018681 Headache, cephalalgia C0003708 Arachnitis HSDN C0424755 Fever symptoms C0040127 Thyroid crisis HSDN C0013421 Dystonia C0010068 Coronary heart disease HSDN C0015672 Decreased energy C0026598 Movement perception HSDN C0007758 Cerebellar ataxia C0037899 Sphingolipidoses HSDN C3887638 Failure to thrive in infant C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO C1963087 Constipation adverse event C1836544 Schindler disease, type i MalaCards C0030193 Sense of pain C4054576 Malignant osteoclastic giant cell-rich tumor of bone UMLS C4084776 Weight loss C0019270 Hernia HSDN C4085211 Pain distress question C0206660 Germinoma HSDN C3665347 Vision impaired C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant HPO C2984057 Have nausea C1999266 Depression adverse event HSDN C0424755 Fever symptoms C0018051 Gonadal dysgenesis HSDN C0039070 Collapse fleeting C1690964 Cataract HSDN C0000737 Abdomen pain C0031269 Peutz-jeghers syndrome MalaCards|HPO C0013604 Edematous C0036875 Disorders of sex development HSDN C0009806 Constipate C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0042963 Symptoms vomiting C2985220 Anaplastic medulloblastoma UMLS C0013421 Dystonia C2931384 Moyamoya disease 1 HSDN C0027497 Queasy C2937421 Prostatic hyperplasia HSDN C3641756 Have diarrhea C0004161 Athletic injuries HSDN C0013604 Edematous C0162316 Iron deficiency anemia HSDN C0700590 Diaphoresis excessive C1334968 Nodular lymphocyte predominant hodgkin lymphoma MalaCards C0023380 Lethargy C1510428 Cerebral abscess HSDN C1557397 Adverse event associated with pain C0013336 Dwarfism HSDN C0013456 Pain ear C0039106 Pigmented villonodular synovitis HSDN C0851578 Disorder sleep C0262584 Carcinoma, small cell HSDN C2024878 Cardiovascular surgery result: dyspnea C0003492 Aortic coarctation HSDN C0042571 Vertigo subjective C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C1557397 Adverse event associated with pain C0751772 Rem sleep behavior disorder HSDN C0030193 Sense of pain C0022876 Premature obstetric labor HSDN C0557874 Global developmental delay C3151781 Ck syndrome MalaCards|HPO C0020903 Illusion C0037774 Spatial behavior HSDN C0242936 Center pain C0014901 Aesthetic HSDN C0030193 Sense of pain C0020540 Malignant hypertension HSDN C0022346 Yellow skin C2981634 Stage ii hilar cholangiocarcinoma UMLS C4084727 Cough frequency C0018799 Heart diseases HSDN C0009460 Communication impairment C0008925 Cleft palate HSDN C0039070 Collapse fleeting C1090821 Sepsis (invertebrate) HSDN C0002962 Angina C0037355 Smallpox vaccines HSDN C0036572 Convulsion C1855255 Pseudoarylsulfatase a deficiency MalaCards|HPO C0004134 Dyssynergia C0850803 Anaphylaxis (non medication) HSDN C0034933 Abnormal reflexes C0221069 Anterior spinal artery syndrome HSDN C0036572 Convulsion C0025323 Menorrhagia HSDN C1549543 Administration method - pain C0023485 Precursor b-cell lymphoblastic leukemia-lymphoma HSDN C0085631 Abnormal excitement C0275148 Poisoning of animal by plant HSDN C0020615 Hypoglycemia nos C2677590 Congenital disorder of glycosylation, type in MalaCards C1384666 Decreased hearing C0949595 Gonadal dysgenesis, 46,xx HPO C0040822 D tremors C2984900 Malignant adrenal gland composite pheochromocytoma UMLS C0038990 Sweats C1859468 Bird headed dwarfism montreal type OrphaNet|MalaCards C1961131 Cough adverse event C3541994 Drug hypersensitivity syndrome MalaCards C1000483 Genus anemia C0085605 Liver failure MalaCards C1963281 Vomiting adverse event C0008370 Cholestasis HSDN C0151786 Weakness muscle C0700327 Clinical findings relating to memory HSDN C1279888 Proteinuria of undiagnosed cause C0029463 Osteosarcoma HSDN C0015469 Facial paralysis C0020649 Hypotension HSDN C0009421 Comatose C0475072 Traumatic cerebral hemorrhage HSDN C0015672 Decreased energy C1532253 Sedentary lifestyle HSDN C0043352 Absent salivary secretion C0001529 Dercum disease MalaCards C0018784 Deafness sensorineural C0002940 Aneurysm HSDN C1963063 Anorexia adverse event C0018802 Congestive heart failure HSDN C0406569 Extensive congenital erosions, vesicles and reticulate scarring C0406567 Collagen and elastic tissue disorders affecting skin UMLS C0030193 Sense of pain C0025427 Mercury poisoning HSDN C0040264 Ear ringing sound C0376175 Bell palsy HSDN C1963247 Ventricular tachycardia adverse event C1854063 Cardiomyopathy dilated with woolly hair and keratoderma MalaCards|HPO C1963063 Anorexia adverse event C1858592 Carney triad MalaCards C0026838 Spasticity muscle C0037937 Spine injury HSDN C0030193 Sense of pain C0006433 Burnout, professional HSDN C0426579 Anorexia symptom C0005967 Bone neoplasms HSDN C4084775 Usual severity weight loss C0432217 Wolcott-rallison syndrome OrphaNet|HPO C4085211 Pain distress question C0524988 Schnitzler syndrome HSDN C0015799 Feminisation C0302826 Expressed emotion HSDN C4084768 Usual severity vomiting C0376532 Epilepsy, rolandic HSDN C1963249 Tinnitus adverse event C1836522 Schindler disease, type ii OrphaNet|HPO C3463815 Feel fatigue C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C1557397 Adverse event associated with pain C0002989 Epithelioid hemangioma of skin HSDN C0042928 Paralysis vocal cord C0038941 Incisional infection HSDN C0011991 Loose stools C0014571 Epiphyses, slipped HSDN C0349588 Stature short C2936910 Cross-mckusick-breen syndrome OrphaNet|MalaCards C4084768 Usual severity vomiting C0220847 C hepatitis virus HSDN C0413252 Hypothermia due to exposure C0878544 Cardiomyopathies HSDN C0015672 Decreased energy C0019557 Hip fx HSDN C0012569 Double vision C0016064 Fibrous dysplasia, monostotic HSDN C0002962 Angina C0080179 Vertebra fracture HSDN C3887638 Failure to thrive in infant C0002395 Alzheimer's disease HSDN C0015938 Fetal macrosomia C0010695 Cystocele HSDN C0003910 Articulation disorder C0344315 Depressed mood HSDN C0018784 Deafness sensorineural C0241158 Cicatrix skin HSDN C0030193 Sense of pain C0027086 Myoma HSDN C0030975 Disorders perception C0002989 Epithelioid hemangioma of skin HSDN C0151786 Weakness muscle C0282607 Vascular neoplasms HSDN C0030193 Sense of pain C0029124 Optic atrophy HSDN C3887638 Failure to thrive in infant C1866259 Peroxisome biogenesis disorder, complementation group 13 MalaCards C0000737 Abdomen pain C0796561 Melanoma vaccines HSDN C0231712 Gait waddling C2752007 Congenital disorder of glycosylation, type io MalaCards|HPO C1549543 Administration method - pain C0013575 Ectodermal dysplasia HSDN C4085211 Pain distress question C0039106 Pigmented villonodular synovitis HSDN C1069915 Vertigo C0020456 Hyperglycemia HSDN C0032617 High urine output C0027726 Nephrotic syndrome HSDN C1963087 Constipation adverse event C0003838 Arterial occlusive diseases HSDN C4084774 Have weight loss C0014849 Esophageal and gastric varices HSDN C0231528 Muscle pain generalized C0026780 Mumps MalaCards C0857305 Thrombocytopenia purpura C0520946 Emotional hypersensitivity HSDN C1279888 Proteinuria of undiagnosed cause C0019069 Hemophilia a HSDN C0162298 Stiffness joints C0003090 Ankylosis UMLS C3539892 Pelvic pain in front C0011854 Diabetes mellitus, insulin-dependent HSDN C0018784 Deafness sensorineural C0020517 Hypersensitivity HSDN C1963065 Apnea adverse event C0003490 Aortic arch syndrome MalaCards C4084768 Usual severity vomiting C2931187 Nephropathic cystinosis MalaCards C1963249 Tinnitus adverse event C0524909 Hepatitis b, chronic HSDN C0030486 Extremity paralysis, lower C0029118 Opportunistic infections HSDN C0231835 Respiration rate increased C0004626 Pneumonia, bacterial HSDN C1384666 Decreased hearing C1368355 Synostosis malformation HSDN C0018772 Deafness C0041755 Adverse reaction to drug HSDN C3898969 Have been vomiting C0035361 Pneumoretroperitoneum HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0030807 Pemphigus, nos HSDN C0497247 Blood pressure elevation C1578691 Congenital myxedema MalaCards C0012833 Dizzy C0022865 Obstetric labor complications HSDN C1956415 Dyspnea paroxysmal nocturnal C0162872 Aortic aneurysm, thoracic MalaCards C0727671 Red cross toothache drops C0149931 Migraine disorders HSDN C0151798 Liver necrosis C0279607 Adult primary hepatocellular carcinoma MalaCards C0036572 Convulsion C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards|UMLS C2315100 Pediatric failure to thrive C2750087 Bile acid malabsorption, primary MalaCards|HPO C0850758 Pain pelvic C0042063 Urogenital abnormalities HSDN C0034933 Abnormal reflexes C0014859 Esophageal neoplasms HSDN C0009806 Constipate C0220981 Metabolic acidosis HSDN C0013421 Dystonia C4015316 Epileptic encephalopathy, early infantile, 27 MalaCards C0030975 Disorders perception C0003873 Rheumatoid arthritis HSDN C0026838 Spasticity muscle C1457883 Aggressive reaction HSDN C2237041 Shox gene with short stature C2931722 Chang davidson carlson syndrome OrphaNet|MalaCards C0018784 Deafness sensorineural C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C2911645 Weight loss adverse event C2931638 Chromosome 8, monosomy 8p23 1 MalaCards C4085548 Usual severity dizziness C0032344 Poisoning aspects HSDN C1000483 Genus anemia C1848561 Methylmalonic acidemia with homocystinuria MalaCards C0242936 Center pain C0042749 Viremia HSDN C0007758 Cerebellar ataxia C0040188 Tic disorder HSDN C0221752 Rbc urine C0268131 Omp decarboxylase deficiency MalaCards C0012833 Dizzy C0270639 Lateral sinus thrombosis HSDN C0020455 Hypergammaglobulinemia C0042974 Von willebrand disease HSDN C0026826 High muscle tone C0270327 Bedwetting HSDN C2237041 Shox gene with short stature C1861306 Synostosis of talus and calcaneus with short stature HPO C0162834 Hyperpigmentation C1961835 Gaucher disease, type 1 MalaCards|HPO C3898969 Have been vomiting C0026769 Multiple sclerosis HSDN C1963137 Hydrocephalus adverse event C1318558 Congenital melanocytic nevus HPO C0031911 Pigment deposition C0334233 Pleomorphic carcinoma MalaCards C0520821 Pluerothotonus C0920233 Pisa syndrome UMLS C0028738 Nystagmus C1838180 Codas syndrome MalaCards|HPO C3539022 Pelvic pain decreasing in severity C0003873 Rheumatoid arthritis HSDN C0036572 Convulsion C2025995 Cellulitis HSDN C0030486 Extremity paralysis, lower C0022665 Kidney neoplasm HSDN C0030193 Sense of pain C0032463 Polycythemia vera HSDN C0497406 Over weight C0010417 Cryptorchidism HSDN C4084897 Sleep disturbance subordinate domain C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C3829611 Nausea frequency C0043065 Water electrolyte imbalance HSDN C0038002 Spleen enlargement C0040028 Thrombocythemia, essential OrphaNet|HPO|MalaCards C0242936 Center pain C2911243 Encounter due to family history of colonic polyps HSDN C0013428 Painful urination C1512746 Infiltrating bladder urothelial carcinoma with giant cells UMLS C0242936 Center pain C0026277 Mixed salivary gland tumor HSDN C0007859 Pain neck C0007097 Carcinomas HSDN C0019079 Bloody sputum C1708650 Laryngeal basaloid carcinoma UMLS C0242936 Center pain C0752235 Lyme neuroborreliosis HSDN C0242936 Center pain C0015652 Fascioliasis HSDN C0700078 Deep tendon reflex decrease C1843164 Charcot-marie-tooth disease, demyelinating, type 1f HPO C2237041 Shox gene with short stature C2678312 Three m syndrome 1 OrphaNet|HPO C0007758 Cerebellar ataxia C1865981 Friedreich ataxia 2 MalaCards C4084802 Usual severity diarrhea C2137063 Ent surgical result - speech HSDN C4084774 Have weight loss C0022408 Arthropathy HSDN C1549543 Administration method - pain C0014548 Epilepsy, generalized HSDN C0085631 Abnormal excitement C0020538 Hypertensive disease HSDN C0018772 Deafness C2316212 Cryopyrin-associated periodic syndromes HSDN C4084766 Vomiting C0205770 Choroid plexus papilloma HSDN|HPO C0038506 Stutter C2370841 Convalescence; treatment HSDN C0015469 Facial paralysis C0023890 Liver cirrhosis HSDN C0020455 Hypergammaglobulinemia C2186740 Reported urticaria HSDN C0454644 Delayed language development C1866927 Smcr HPO C4085210 Usual severity pain C0015806 Femur neck fracture HSDN C0043094 Weight gain C1135821 Mortality syndrome, spiking HSDN C0040264 Ear ringing sound C0024530 Malaria HSDN C0007758 Cerebellar ataxia C0043388 Bouba HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027819 Neuroblastoma HSDN C3898969 Have been vomiting C0405580 Adrenal cortical hypofunction HSDN C0237326 Defecation pain C1970431 Pitt-hopkins syndrome MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0038463 Strongyloides infection HSDN C0018808 Murmur C0008625 Chromosome aberrations HSDN C0009676 Confusion state C0014549 Tonic-clonic epilepsy HSDN C1963087 Constipation adverse event C0033975 Psychotic disorders HSDN C0522224 Palsied C0024694 Mandibular neoplasms HSDN C0700078 Deep tendon reflex decrease C4015038 Myasthenic syndrome, congenital, 7, presynaptic MalaCards C0234523 Apraxia, classic C0020179 Huntington disease HSDN C1963249 Tinnitus adverse event C0040997 Trigeminal neuralgia HSDN C4084769 Vomiting frequency C0020303 Hydropneumothorax HSDN C0015672 Decreased energy C0026771 Trauma multiple HSDN C0277799 Fever intermittent C1851347 Familial mediterranean fever, autosomal dominant HPO C0000737 Abdomen pain C0015806 Femur neck fracture HSDN C4084768 Usual severity vomiting C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0020455 Hypergammaglobulinemia C0030567 Parkinson disease HSDN C0007859 Pain neck C0810056 Spondylosis; intervertebral disc disorders; other back problems UMLS C1961131 Cough adverse event C1800706 Idiopathic pulmonary fibrosis MalaCards|HSDN C4042891 Sleep wake disorders C2911643 Encounter due to family history of osteoporosis HSDN C4084727 Cough frequency C0018671 Head and neck neoplasms HSDN C0040822 D tremors C1860157 Elejalde disease MalaCards C3463815 Feel fatigue C3665349 Secondary hypothyroidism OrphaNet|MalaCards C0026821 Cramp C0004044 Asphyxia HSDN C0035232 Diaphragmatic paralysis C1458155 Mammary neoplasms HSDN C0522224 Palsied C0023798 Lipoma HSDN C0587047 Mass of trunk C0451714 Hep granulomas in berylliosis UMLS C0018524 Hallucinate C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C0024031 Back pain lower back C0037929 Spinal cord injuries HSDN C0005745 Blepharoptosis C1302995 Congenital fibrosis of the extraocular muscles MalaCards C0018681 Headache, cephalalgia C1704212 Embolism embolus HSDN C0878773 Bladder hyperactive C1270972 Mild cognitive disorder HSDN C0003862 Pain joint C0085655 Polymyositis OrphaNet|MalaCards C0009676 Confusion state C0014077 Leukoencephalitis, acute hemorrhagic HSDN C3887638 Failure to thrive in infant C1864689 Microphthalmia, syndromic 6 (disorder) MalaCards|HPO C0151889 Reflexes tendon increased C1412397 Ancr gene HPO C0011570 Monopolar depression C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0003126 Smell loss C0271581 Isolated follitropin deficiency MalaCards C0162323 Arthritis, multiple joint involvement C1851347 Familial mediterranean fever, autosomal dominant HPO C0413252 Hypothermia due to exposure C0848377 Trauma to the abdomen HSDN C4084776 Weight loss C0037417 Identification, social HSDN C1279888 Proteinuria of undiagnosed cause C1839874 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis OrphaNet C4084775 Usual severity weight loss C0014038 Encephalitis HSDN C1557397 Adverse event associated with pain C1963282 Wolff-parkinson-white syndrome adverse event HSDN C0039070 Collapse fleeting C0011609 Drug eruptions HSDN C4084776 Weight loss C0041466 Typhoid fever HSDN C0151786 Weakness muscle C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C3641756 Have diarrhea C0038663 Suicide attempt HSDN C3887638 Failure to thrive in infant C0410180 Eichsfeld type congenital muscular dystrophy HPO C1549543 Administration method - pain C0003047 Animal disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1135841 Zoster sine eruptione HSDN C0349588 Stature short C1844918 Branchial arch syndrome, x-linked OrphaNet|MalaCards C4085211 Pain distress question C0040137 Thyroid nodule HSDN C1963252 Tremor adverse event C0796222 Mental retardation, x linked 16 MalaCards|HPO C0022568 Inflammation corneal C0043194 Wiskott-aldrich syndrome MalaCards|HPO C2984057 Have nausea C1963119 Stomach ulcer adverse event HSDN C0575081 Abnormal gait C0035410 Rhabdomyolysis MalaCards C3641755 Have constipation C0006663 Calcinosis HSDN C0030193 Sense of pain C1546847 Entity name part type - family HSDN C0036572 Convulsion C0036357 Psychology, schizophrenic HSDN C0575081 Abnormal gait C0004943 Behcet syndrome OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0010034 Corneal diseases HSDN C0013421 Dystonia C0039082 Syndrome HSDN C0018681 Headache, cephalalgia C0035053 Spontaneous remission HSDN C0018681 Headache, cephalalgia C0280475 Childhood oligodendrogliomas UMLS C4085548 Usual severity dizziness C0017636 Glioblastoma HSDN C0003469 Anxiety disorder C1136033 Cutaneous mastocytosis MalaCards C1963087 Constipation adverse event C0034065 Pulmonary embolism HSDN C2029884 Hearing loss by exam C0011581 Depressive disorder HSDN C2237041 Shox gene with short stature C3714043 Trisomy xq28 OrphaNet|HPO C2096293 Ent surgical result ear vertigo C1690964 Cataract HSDN C4084802 Usual severity diarrhea C0021843 Intestinal obstruction HSDN C0233470 Affect constricted C1291710 Disturbances of affect UMLS C4085862 Bothered by nausea C4042784 Feeding and eating disorders HSDN C1549543 Administration method - pain C0000817 Abortion septic HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C0036202 Sarcoidosis MalaCards|HPO C0013421 Dystonia C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards|HPO C2911645 Weight loss adverse event C0002871 Anemia HSDN C0349588 Stature short C3151185 Short-rib thoracic dysplasia 4 with or without polydactyly MalaCards|HPO C0030552 Paralysis partial C0152109 Juvenile spinal muscular atrophy HPO C4020887 Photodysphoria C1848412 Trichothiodystrophy with sun sensitivity HPO C0005745 Blepharoptosis C2700265 Waardenburg syndrome type 2 HPO C0232943 Metromenorrhagia C3647157 Other gynecologic disorders UMLS C0026826 High muscle tone C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C2239176 Liver carcinoma MalaCards|HSDN C0011124 Libido decreased C0549622 Sexual dysfunction UMLS C1963093 Dizziness adverse event C0038356 Stomach neoplasms HSDN C1069915 Vertigo C1720416 Episodic ataxia type 2 (disorder) MalaCards|HPO C3539022 Pelvic pain decreasing in severity C0023903 Liver neoplasms HSDN C2024878 Cardiovascular surgery result: dyspnea C0008625 Chromosome aberrations HSDN C0009806 Constipate C0001430 Adenoma HSDN C2919142 Short stature adverse event C1864851 Pigmented nodular adrenocortical disease, primary, 2 MalaCards C0022107 Fussiness C0175683 Citrullinemia HPO C3898969 Have been vomiting C0014854 Esophageal diverticulum HSDN C2315100 Pediatric failure to thrive C1846545 Autoimmune lymphoproliferative syndrome type 2b HPO C4085661 Usual severity nausea C0002940 Aneurysm HSDN C0018775 Hearing loss bilateral C0008628 Chromosome deletion HSDN C3146279 Coma C0036344 Schizophrenia, catatonic HSDN C0012833 Dizzy C1000483 Genus anemia HSDN C1962972 Proteinuria adverse event C0024530 Malaria HSDN C4084776 Weight loss C0009373 Colonic diseases HSDN C0007398 Catatonic C0085271 Self-injurious behavior HSDN C1962957 Flushing adverse event C0027051 Myocardial infarction HSDN C0851578 Disorder sleep C0042345 Varicosity HSDN C0013362 Dysarthrias C0238027 Botulism, infantile OrphaNet|MalaCards C1069915 Vertigo C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C3641755 Have constipation C0020456 Hyperglycemia HSDN C0013395 Indigestion C0024232 Lymphatic metastasis HSDN C0020673 Hypothermia (central) (local) C0014118 Endocarditis HSDN C3274924 Have been coughing C0029463 Osteosarcoma HSDN C0013421 Dystonia C0002792 Anaphylaxis HSDN C0033774 Skin pruritus C0004275 Attitude health HSDN C2919142 Short stature adverse event C0398739 Congenital disorder of glycosylation, type 2c MalaCards|HPO C1557397 Adverse event associated with pain C1138434 Disease, x-linked genetic HSDN C4084802 Usual severity diarrhea C0025269 Multiple endocrine neoplasia type 2b HPO C0030193 Sense of pain C0024689 Mandibular diseases HSDN C0024031 Back pain lower back C0009319 Colitis HSDN C0497247 Blood pressure elevation C1706004 Anhydrotic ectodermal dysplasias MalaCards C0038002 Spleen enlargement C0268255 Farber lipogranulomatosis MalaCards|HPO C0036396 Sciatica C1963064 Anxiety adverse event HSDN C0851578 Disorder sleep C0238288 Muscular dystrophy, facioscapulohumeral HSDN C1963252 Tremor adverse event C2911643 Encounter due to family history of osteoporosis HSDN C0428977 Pulse rate decrease C0268381 Primary amyloidosis MalaCards C4085211 Pain distress question C0006012 Borderline personality disorder HSDN C0011206 Delirium acute C0037199 Sinusitis HSDN C0033774 Skin pruritus C2987190 Pancreatic intraductal tubulopapillary neoplasm with an associated invasive carcinoma UMLS C1963281 Vomiting adverse event C0042830 Perception visual HSDN C3641755 Have constipation C0017636 Glioblastoma HSDN C3898969 Have been vomiting C2137063 Ent surgical result - speech HSDN C3887638 Failure to thrive in infant C1846421 Lathosterolosis OrphaNet|HPO|MalaCards C0036396 Sciatica C0011570 Mental depression HSDN C0018772 Deafness C0011853 Diabetes mellitus, experimental HSDN C0454644 Delayed language development C0878684 Short syndrome MalaCards|HPO C4085211 Pain distress question C0302182 Trabecular adenocarcinoma MalaCards C0010200 Cough symptom C0007682 Cns disorder HSDN C0522357 Vertigo paroxysmal C0334419 Pheochromocytoma, malignant MalaCards C0242936 Center pain C0018889 Helminthiasis HSDN C0013604 Edematous C0024248 Cyst lymph HSDN C0004093 Asthenia C0026896 Myasthenia gravis HSDN C0004134 Dyssynergia C0268542 Ornithine carbamoyltransferase deficiency HSDN C1971624 Appetite absent C0022658 Kidney diseases HSDN C1321898 Bloody stool C0030922 Peptic ulcer hemorrhage UMLS C0026821 Cramp C0001418 Adenocarcinoma HSDN C0010038 Corneal opacity disorder C1854896 Mucolipidosis iii gamma MalaCards C0040034 Thrombocytopenia C1866423 Quebec platelet disorder MalaCards|HPO C0518090 Frequency of pain question C0034362 Q fever HSDN C0427055 Face weakness C3280402 Sclerosteosis 2 MalaCards C0020578 Hyperventilate C0546884 Hypovolemia HSDN C2024893 Cardiovascular surgery result: fatigue C0030581 Parotid neoplasms HSDN C2984058 Have pain C2188545 Anuria HSDN C1384666 Decreased hearing C0001726 Affective symptoms HSDN C0042798 Vision dim C1458155 Mammary neoplasms HSDN C0033377 Caudal displacement C1864649 Myasthenia, limb-girdle, with tubular aggregates HPO C1549543 Administration method - pain C0006114 Cerebral edema HSDN C4085222 Nausea C1457883 Aggressive reaction HSDN C1579931 Depressed - symptom C1864112 Huntington disease-like 1 MalaCards|HPO C4084723 Constipation C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C3539893 Pelvic pain occurs with intercourse C2936290 Femoracetabular impingement HSDN C4084769 Vomiting frequency C0043246 Laceration HSDN C0042024 Urine incontinence C0024919 Behavior, maternal HSDN C3539895 Pelvic pain occurs with bowel movement C0037856 Spermatic cord torsion HSDN C3887784 Decreased urine output C0014544 Epilepsy HSDN C0476250 Head neck mass C1290120 Melanocytic naevus of scalp UMLS C0427068 Legs weakness C1853251 Spastic paraplegia 33, autosomal dominant MalaCards|HPO C1549543 Administration method - pain C0040765 Transsexualism HSDN C0009806 Constipate C0268242 Niemann-pick disease, type a MalaCards|HPO|UMLS C3539890 Pelvic pain causes awakening at night C1261473 Sarcoma HSDN C0043094 Weight gain C0860603 Anxiety symptoms HSDN C0151786 Weakness muscle C0037397 Behavior social HSDN C0009806 Constipate C0030567 Parkinson disease MalaCards C0009421 Comatose C0007361 Cat-scratch disease HSDN C4085862 Bothered by nausea C1847843 Episodic ataxia, type 4 MalaCards C1145670 Failure respiratory C2931047 Hecht scott syndrome OrphaNet C0362036 Coma and stupor nos C0085628 Stupor UMLS C0349506 Sun sensitivity C1848413 Trichothiodystrophy, type 1 MalaCards|HPO C2108113 Continuous electrocardiogram ventricular tachycardia C2678476 Cardiomyopathy, dilated, 1y MalaCards|HPO C2203646 Jaundice C4045991 Perihilar cholangiocarcinoma MalaCards C0020580 Decreased sensation C0033578 Prostatic neoplasms HSDN C2984058 Have pain C0007121 Bronchogenic carcinoma HSDN C0020903 Illusion C0014901 Aesthetic HSDN C0043094 Weight gain C0014544 Epilepsy HSDN C4085211 Pain distress question C0039504 Injuries tendon HSDN C0020615 Hypoglycemia nos C2678408 Pituitary hormone deficiency, combined, 4 MalaCards|HPO C1963093 Dizziness adverse event C0003813 Arrhythmia sinus HSDN C4084773 Bothered by weight gain C0024141 Lupus erythematosus, systemic HSDN C0042963 Symptoms vomiting C0018133 Graft-vs-host disease HSDN C0149793 Transient monocular blindness C1706192 Sulfatidosis MalaCards C0233514 Behavior abnormal C0393590 Fahr's syndrome (disorder) MalaCards C0004134 Dyssynergia C0085292 Stiff-person syndrome HSDN C0015970 Fever unknown origin C0010356 Cross infection HSDN C0004604 Pain back C0085435 Arthritis, reactive MalaCards C0018777 Deafness, conductive C0042373 Vascular diseases HSDN C0042571 Vertigo subjective C0022738 Klippel-feil syndrome HSDN C4084788 Have dizziness C0017563 Gingival diseases HSDN C0020673 Hypothermia (central) (local) C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C4084766 Vomiting C0024215 Lymphangiectasis, intestinal HSDN C0027066 Myoclonic jerking C0037019 Shy-drager syndrome HSDN C4084769 Vomiting frequency C1704436 Peripheral arterial diseases HSDN C0042024 Urine incontinence C0013806 Electroplexy shock therapy HSDN C3203358 Alveolar hypoventilation C0040053 Thrombosis HSDN C0041657 Consciousness loss C0038663 Suicide attempt HSDN C4084802 Usual severity diarrhea C0027121 Myositis HSDN C2203646 Jaundice C0036412 Sclera HSDN C0020903 Illusion C0001721 Emotional affect HSDN C0030193 Sense of pain C0029927 Ovarian cysts HSDN C0080233 Dental loss C1968804 Plasminogen deficiency, type i MalaCards C0038002 Spleen enlargement C0086650 Mps iii d HPO C0035232 Diaphragmatic paralysis C0428977 Bradycardia HSDN C0030193 Sense of pain C2051831 Pectus excavatum HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011849 Diabetes mellitus HSDN C0011991 Loose stools C1832322 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive HPO|UMLS C2984057 Have nausea C1962983 Cataract adverse event HSDN C4085317 Diarrhea frequency C0025323 Menorrhagia HSDN C0018772 Deafness C0040820 Trematode infections HSDN C0030552 Paralysis partial C0025202 Melanoma HSDN C0002170 Alopecia disorders C0018522 Hallermann's syndrome OrphaNet|MalaCards C1384666 Decreased hearing C4049644 Depression HSDN C0221232 Welts C0263334 Aquagenic urticaria UMLS C3463815 Feel fatigue C0600519 Ventricular remodeling HSDN C2700617 Irritation - emotion C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0242936 Center pain C0001075 Achlorhydria HSDN C3665346 Loss sight C0205710 Alpers syndrome (disorder) MalaCards|HPO|UMLS C0036572 Convulsion C1332187 Adult brain glioblastoma UMLS C1963086 Confusion adverse event C0015630 Fantasies HSDN C4084767 Bothered by vomiting C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C1961131 Cough adverse event C0027932 Neurotic disorders HSDN C4084724 Usual severity constipation C1869118 Hypothyroidism, congenital, due to thyroid dysgenesis HPO C2984058 Have pain C0020428 Hyperaldosteronism HSDN C3146279 Coma C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C1963086 Confusion adverse event C1532265 Encephalitis caused by siberian tick-borne encephalitis virus MalaCards C0522224 Palsied C0017636 Glioblastoma MalaCards|HSDN C0034155 Thrombotic thrombocytopenic purpura C2188545 Anuria HSDN C0026838 Spasticity muscle C0037933 Spinal diseases HSDN C0013604 Edematous C0003469 Anxiety disorders HSDN C0036572 Convulsion C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards C1069915 Vertigo C0270611 Brain damage HSDN C4084784 Diarrhea C0001627 Congenital adrenal hyperplasia HSDN C0031911 Pigment deposition C0025202 Melanoma MalaCards C1963249 Tinnitus adverse event C0062527 Hepatitis b vaccine HSDN C2984057 Have nausea C3489393 Hiatal hernia HSDN C0030552 Paralysis partial C0018794 Heart block HSDN C0009806 Constipate C1333074 Cloacogenic carcinoma of rectum UMLS C0020578 Hyperventilate C0017658 Glomerulonephritis HSDN C1384666 Decreased hearing C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0349588 Stature short C0282529 Chondrodysplasia punctata, rhizomelic OrphaNet|MalaCards C3641756 Have diarrhea C0853697 Neutrophil count decreased HSDN C0848203 Male pelvic pain C0022661 Kidney failure, chronic HSDN C0038868 Supranuclear palsy progressive C0009240 Cognition HSDN C4084784 Diarrhea C0008325 Cholecystitis HSDN C0036572 Convulsion C1856057 Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type HPO|UMLS C0233794 Memory impaired C2931917 Alcoholic encephalopathy MalaCards C0241137 Skin pallor C1848561 Methylmalonic acidemia with homocystinuria MalaCards C0020455 Hypergammaglobulinemia C0268250 Gaucher disease, type 2 (disorder) MalaCards C1549543 Administration method - pain C0003892 Neurogenic arthropathy HSDN C2242996 Tingling C0009730 Spinal meningocele HSDN C2984057 Have nausea C0518450 Spinal fractures HSDN C1963087 Constipation adverse event C1963119 Stomach ulcer adverse event HSDN C0030554 Abnormal sensation C0003850 Arteriosclerosis HSDN C4084766 Vomiting C0037036 Sialorrhea HSDN C1962972 Proteinuria adverse event C3280113 Nephrotic syndrome, type 5, with or without ocular abnormalities MalaCards C4084724 Usual severity constipation C0033860 Psoriasis HSDN C0007398 Catatonic C0011854 Diabetes mellitus, insulin-dependent HSDN C3494358 Characteristic, prodromal C0795623 Hepatitis a vaccine, inactivated HSDN C0349588 Stature short C1876203 Frontonasal dysplasia MalaCards C0018784 Deafness sensorineural C0041948 Uremia HSDN C0009080 Finger clubbing C0345893 Juvenile polyposis syndrome HPO C0151827 Pain eye C0042162 Uveal neoplasms HSDN C0000737 Abdomen pain C0006434 Burn injury HSDN C4084776 Weight loss C0023904 Liver neoplasms, experimental HSDN C3539020 Pelvic pain decreasing in frequency C0001261 Actinomycosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014457 Eosinophilia HSDN C3539023 Pelvic pain increasing in frequency C0033046 Premenstrual syndrome HSDN C0011206 Delirium acute C0004096 Asthma HSDN C0013390 Cramps menstrual C0007097 Carcinomas HSDN C1963184 Nystagmus adverse event C3808786 Albinism, oculocutaneous, type vii MalaCards C0007758 Cerebellar ataxia C0752160 Hemangioma, cavernous, central nervous system HSDN C3241945 Melena due to gastrointestinal hemorrhage C0042470 Guanarito haemorrhagic fever MalaCards C0015672 Decreased energy C0042338 Herpesvirus 3, human HSDN C0039070 Collapse fleeting C0006147 Breast fed HSDN C0018524 Hallucinate C0007771 Intracranial arteriosclerosis HSDN C1557397 Adverse event associated with pain C0032580 Adenomatous polyposis coli HSDN C1963281 Vomiting adverse event C0242383 Age related macular degeneration HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2350529 Pulmonary aspergillosis HSDN C4084775 Usual severity weight loss C0040336 Tobacco use disorder HSDN C0020505 Excessive eating C0023895 Liver diseases HSDN C3641756 Have diarrhea C0282207 Cronkhite-canada syndrome OrphaNet|MalaCards C1963091 Diarrhea adverse event C2350019 Solitary pulmonary nodule HSDN C0026838 Spasticity muscle C0032371 Poliomyelitis HSDN C0028738 Nystagmus C1836797 Combined oxidative phosphorylation deficiency 1 MalaCards|HPO C2237041 Shox gene with short stature C1855080 Microcephaly-cardiomyopathy syndrome MalaCards C0022346 Yellow skin C0342859 Harderoporphyria HPO C0542476 Forgetful C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C1963252 Tremor adverse event C1000483 Genus anemia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1550639 Specimen type - fistula HSDN C0042963 Symptoms vomiting C2711266 Infection by anisakis larva HSDN C0027066 Myoclonic jerking C0024530 Malaria HSDN C4085317 Diarrhea frequency C0029434 Osteogenesis imperfecta HSDN C1279888 Proteinuria of undiagnosed cause C0000771 Abnormalities, drug induced HSDN C0042755 Virilisation C0022661 Kidney failure, chronic HSDN C1963087 Constipation adverse event C3827868 Tachycardia by ecg finding HSDN C0027066 Myoclonic jerking C0007001 Carbohydrate metabolism, inborn errors HSDN C0917816 Deficiency mental C3463992 Epileptic encephalopathy, early infantile, 1 MalaCards C4084767 Bothered by vomiting C1959626 Mevalonic aciduria MalaCards|HPO C4084727 Cough frequency C0043254 Injuries penetrating HSDN C4085317 Diarrhea frequency C0022876 Premature obstetric labor HSDN C0036572 Convulsion C0393698 Cryptogenic infantile spasms UMLS C4084767 Bothered by vomiting C0025281 Meniere disease HSDN C0085636 Light sensitivity C3665333 Keratitis-ichthyosis-deafness syndrome OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0030920 Peptic ulcer HSDN C4085661 Usual severity nausea C0038354 Stomach diseases HSDN C0424755 Fever symptoms C0035579 Rickets HSDN C2700617 Irritation - emotion C0005283 Beta thalassemia OrphaNet C0003079 Pupillary inequality C0007766 Intracranial aneurysm HSDN C0018524 Hallucinate C0022701 Kinesthesia HSDN C0013604 Edematous C0007787 Transient ischemic attack HSDN C4020887 Photodysphoria C1853959 Birdshot chorioretinopathy OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0023434 Chronic lymphocytic leukemia HSDN C0012833 Dizzy C0026640 Mouth neoplasms HSDN C0022346 Yellow skin C0013922 Embolism HSDN C4084775 Usual severity weight loss C0242707 Ventricular dysfunction, right HSDN C0018772 Deafness C1846056 Abidi x-linked mental retardation syndrome OrphaNet C1962972 Proteinuria adverse event C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C0003962 Ascites C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0518090 Frequency of pain question C0009730 Spinal meningocele HSDN C0036572 Convulsion C0016045 Fibroma HSDN C1069915 Vertigo C0011849 Diabetes mellitus HSDN C3641756 Have diarrhea C0024198 Lyme disease HSDN C1000483 Genus anemia C2675526 Neutropenia, severe congenital, autosomal recessive 4 HPO C2984057 Have nausea C0554114 Epstein-barr virus hepatitis MalaCards C3665347 Vision impaired C4041558 Cone-rod synaptic disorder, congenital nonprogressive MalaCards C0042025 Urinary incontinence stress C0004096 Asthma HSDN C2984058 Have pain C0024895 Bovine mastitis HSDN C0349588 Stature short C3280489 Feingold syndrome 2 MalaCards C0242936 Center pain C0358297 Anthrax vaccines HSDN C0151889 Reflexes tendon increased C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant OrphaNet|HPO C4084788 Have dizziness C0037929 Spinal cord injuries HSDN C0426579 Anorexia symptom C0453996 Tobacco smoking HSDN C4084769 Vomiting frequency C0242216 Biliary calculi HSDN C1963071 Back pain adverse event C1963137 Hydrocephalus adverse event HSDN C1963086 Confusion adverse event C1548578 Location characteristic id - smoking HSDN C0752303 Manifestation, urological C0021053 Immune system diseases HSDN C4084773 Bothered by weight gain C0005941 Bone diseases, developmental HSDN C0010200 Cough symptom C1535939 Pneumocystis jiroveci pneumonia HSDN|UMLS C2203646 Jaundice C1306571 Hepatic insufficiency HSDN C0231218 Malaise generalized C3273032 Lymphoepithelioma-like hepatocellular carcinoma UMLS C1090821 Sepsis C0041188 Pyomyositis, tropical MalaCards C1549543 Administration method - pain C0024312 Lymphopenia HSDN C0013404 Respiratory difficulty C0085436 Meningitis, cryptococcal UMLS C4084767 Bothered by vomiting C0002514 Amino acid metabolism, inborn errors HSDN C0028738 Nystagmus C0751664 Canavan disease, neonatal MalaCards C0003862 Pain joint C0004096 Asthma HSDN C4084897 Sleep disturbance subordinate domain C1866927 Smcr HPO C0013421 Dystonia C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0030567 Parkinson disease HSDN C1963137 Hydrocephalus adverse event C0220769 Fg syndrome MalaCards|HPO C3641756 Have diarrhea C0037997 Splenic diseases HSDN C0274369 Pain due to any device, implant or graft C2106863 Pain due to orthopedic device, implant, or graft UMLS C0235031 Neurological complaint C0476214 Post syndrome viral UMLS C2203646 Jaundice C2020541 Strabismus HSDN C1527340 Abnormal voice C1849348 Richieri costa pereira syndrome MalaCards C0557874 Global developmental delay C1848561 Methylmalonic acidemia with homocystinuria OrphaNet|HPO|MalaCards C0333252 Myxedema, localized C2584703 Endemic congenital iodine deficiency syndrome of myxedematous type UMLS C4084784 Diarrhea C1306503 Congenital exomphalos HSDN C4084725 Usual severity cough C0009244 Behavioral cognitive therapy HSDN C0917816 Deficiency mental C1859468 Bird headed dwarfism montreal type OrphaNet|MalaCards C0015230 Exanthem C0546948 Enterovir exanthematous fever UMLS C1963093 Dizziness adverse event C0340493 Paroxysmal familial ventricular fibrillation MalaCards C2984058 Have pain C0020555 Hypertrichosis HSDN C0008031 Pain chest C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0008031 Pain chest C0021655 Insulin resistance HSDN C1963065 Apnea adverse event C0006266 Bronchial spasm HSDN C4084775 Usual severity weight loss C0029132 Disorder of the optic nerve HSDN C0003467 Angst C1868681 Dystonia 12 HPO C1963091 Diarrhea adverse event C0022602 Actinic keratosis HSDN C0030552 Paralysis partial C0272295 Purpura, rheumatica MalaCards C0027796 Neuralgias C0022116 Ischemia HSDN C2700617 Irritation - emotion C0038868 Progressive supranuclear palsy HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0152177 Trigeminal neuropathy HSDN C0038506 Stutter C2984572 Malaria pathway HSDN C0231528 Muscle pain generalized C0040149 Subacute thyroiditis HSDN C0027497 Queasy C0007760 Cerebellar diseases HSDN C2911647 Weight gain adverse event C0035304 Retinal degeneration HSDN C1384666 Decreased hearing C0027658 Neoplasms, germ cell and embryonal HSDN C0413252 Hypothermia due to exposure C0019348 Herpes simplex infections HSDN C0036572 Convulsion C0265321 Wyburn-mason syndrome OrphaNet|MalaCards C0700590 Diaphoresis excessive C1859049 Cchs with hirschsprung disease MalaCards|HPO C0037771 Paraparesis spastic C2750442 Hypermanganesemia with dystonia polycythemia and cirrhosis HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0037397 Behavior social HSDN C1963065 Apnea adverse event C0004144 Atelectasis HSDN C0027497 Queasy C0861854 Adenosquamous bile duct carcinoma UMLS C0042798 Vision dim C1845446 Corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia HPO C3539023 Pelvic pain increasing in frequency C0432264 Axial osteosclerosis MalaCards C4085661 Usual severity nausea C0162820 Dermatitis, allergic contact HSDN C0011991 Loose stools C0029001 Onchocerciasis HSDN C0003469 Anxiety disorder C0751435 Hyperphenylalaninaemia MalaCards C0018520 Breath odor C0035455 Rhinitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0006114 Cerebral edema HSDN C0040460 Dental pain C0032787 Postoperative complications HSDN C4085210 Usual severity pain C0585442 Osteosarcoma of bone HSDN C0007166 Cardiac output decreased C0023895 Liver diseases HSDN C0015672 Decreased energy C1848814 Thymoma, familial MalaCards C0426579 Anorexia symptom C0024530 Malaria HSDN C0476250 Head neck mass C0027961 Nevus of ota UMLS C4085862 Bothered by nausea C0016057 Fibrosarcoma HSDN C0033377 Caudal displacement C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C0232466 Feeding difficulty C1864843 Combined oxidative phosphorylation deficiency 2 MalaCards C4084769 Vomiting frequency C0017668 Focal glomerulosclerosis HSDN C0020649 Blood pressure decreased C0342200 Endemic cretinism MalaCards C1557397 Adverse event associated with pain C0041188 Pyomyositis, tropical HSDN C0002622 Amnesias C0025284 Meningeal neoplasms HSDN C0151786 Weakness muscle C0006057 Botulisms MalaCards C0004134 Dyssynergia C0016756 Fructose-1,6-diphosphatase deficiency HSDN C0557874 Global developmental delay C2931743 Lactate dehydrogenase deficiency type a MalaCards C1963137 Hydrocephalus adverse event C3280766 Joubert syndrome 14 MalaCards C1963170 Hypothermia adverse event C2240374 Eosinophil count raised HSDN C0151786 Weakness muscle C0039984 Thoracic outlet syndrome OrphaNet|HSDN|MalaCards C2911645 Weight loss adverse event C0003838 Arterial occlusive diseases HSDN C0476250 Head neck mass C0266562 Retinal haemangioblastomatosis UMLS C2237041 Shox gene with short stature C0796202 Wittwer syndrome MalaCards C0020455 Hypergammaglobulinemia C1175175 Severe acute respiratory syndrome HSDN C4084802 Usual severity diarrhea C0003650 Apudoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0003493 Aortic diseases HSDN C0035229 Respiratory function impaired C3489726 Geleophysic dysplasia MalaCards C4084768 Usual severity vomiting C0042373 Vascular diseases HSDN C0009676 Confusion state C3812171 Bradycardia by ecg finding HSDN C0917816 Deficiency mental C3890167 Mental retardation, x-linked 100 MalaCards C0016382 Cutaneous vascular engorgement C0398691 Hyperimmunoglobulinemia d MalaCards|HPO C0151786 Weakness muscle C0028738 Nystagmus HSDN C4084767 Bothered by vomiting C0032066 Plague vaccines HSDN C3496180 Sleep apnea C1846171 Lissencephaly, x-linked, 2 MalaCards C0018681 Headache, cephalalgia C0376300 Dengue shock syndrome OrphaNet|MalaCards C2984058 Have pain C2004491 Cicatrix HSDN C0917816 Deficiency mental C2674574 Aortic aneurysm, familial thoracic 3 MalaCards C0027498 Nausea vomiting C0376300 Dengue shock syndrome MalaCards C1962972 Proteinuria adverse event C0032019 Pituitary neoplasms HSDN C0036572 Convulsion C2678416 Hyperphenylalaninemia, non-pku mild HPO C1549543 Administration method - pain C3245466 Observationvalue - trust HSDN C0030486 Extremity paralysis, lower C0023890 Liver cirrhosis HSDN C0853698 Lymphocytes increased C0220989 Acquired partial lipodystrophy OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0011882 Diabetic neuropathies HSDN C0027796 Neuralgias C0001122 Acidosis HSDN C2237041 Shox gene with short stature C2675511 Diamond-blackfan anemia 8 MalaCards C0424755 Fever symptoms C0022362 Jaw diseases HSDN C0917816 Deficiency mental C3554209 Pontocerebellar hypoplasia, type 8 MalaCards C0518090 Frequency of pain question C3495801 Granulomatosis with polyangiitis HSDN C0242936 Center pain C0018994 Hemobilia HSDN C0004604 Pain back C0027643 Neoplasm recurrence, local HSDN C0004134 Dyssynergia C2751318 Nijmegen breakage syndrome-like disorder MalaCards|HPO C0151686 Growth retardation C0041408 Turner syndrome OrphaNet C0007758 Cerebellar ataxia C0342731 Deficiency of mevalonate kinase OrphaNet|HSDN|HPO|MalaCards C1557397 Adverse event associated with pain C0041976 Urethritis HSDN C0013362 Dysarthrias C0009404 Colorectal neoplasms HSDN C4076169 Pain following cerebrovascular accident C0038454 Cerebrovascular accident UMLS C0851578 Disorder sleep C0011616 Contact dermatitis HSDN C0001825 Agraphia C4049644 Depression HSDN C0002170 Alopecia disorders C0004943 Behcet syndrome MalaCards C0018681 Headache, cephalalgia C0025202 Melanoma HSDN C2984058 Have pain C0025064 Mediastinitis HSDN C0600142 Flash hot C1548578 Location characteristic id - smoking HSDN C0016382 Cutaneous vascular engorgement C0026691 Mucocutaneous lymph node syndrome OrphaNet|MalaCards C3887784 Decreased urine output C2347126 Microscopic polyarteritis MalaCards C0010200 Cough symptom C0038160 Staphylococcal infections HSDN C4084725 Usual severity cough C0018671 Head and neck neoplasms HSDN C0034150 Skin purpura C1366464 F9 gene HSDN C0022346 Yellow skin C0042214 Vaccinia HSDN C2024893 Cardiovascular surgery result: fatigue C2930815 Acute cerebral gaucher disease MalaCards C0030193 Sense of pain C2242765 Acquired spondylolisthesis HSDN C0013428 Painful urination C0041311 Tuberculosis, female genital HSDN C0518090 Frequency of pain question C0025472 Mesenteric vascular occlusion HSDN C2024893 Cardiovascular surgery result: fatigue C0014859 Esophageal neoplasms HSDN C4085222 Nausea C0004623 Bacterial infections HSDN C4085210 Usual severity pain C0085395 Ureaplasma infections HSDN C0860603 Anxiety symptom C0031485 Phenylketonurias MalaCards C3463815 Feel fatigue C0017205 Gaucher disease OrphaNet|MalaCards C0495677 Hypoaesthesia of skin C0154725 Oth disorder nervous system UMLS C0000737 Abdomen pain C2984572 Malaria pathway HSDN C0349588 Stature short C0024454 Maffucci syndrome OrphaNet|HPO|MalaCards C0020505 Excessive eating C1857854 Proopiomelanocortin deficiency OrphaNet|HPO C2315100 Pediatric failure to thrive C1420653 Tcn2 gene HPO C1145670 Failure respiratory C0175778 Larsen syndrome MalaCards|HPO C3274924 Have been coughing C0006663 Calcinosis HSDN C3274924 Have been coughing C0017612 Glaucoma, open-angle HSDN C0151827 Pain eye C0027873 Neuromyelitis optica MalaCards C0010200 Cough symptom C0020542 Pulmonary hypertension HSDN C0151786 Weakness muscle C0085433 Acquired joint deformities HSDN C0349506 Sun sensitivity C1851443 Cerebrooculofacioskeletal syndrome 3 MalaCards|HPO C3539893 Pelvic pain occurs with intercourse C0006434 Burn injury HSDN C0026821 Cramp C0034065 Pulmonary embolism HSDN C0022346 Yellow skin C2981638 Stage ivb hilar cholangiocarcinoma UMLS C0036572 Convulsion C2931870 Familial schizencephaly MalaCards C0007758 Cerebellar ataxia C0342727 3-@methylglutaconic aciduria, type i MalaCards|HPO|UMLS C3665347 Vision impaired C0878677 Glycogen storage disease type iib MalaCards|HPO C0009792 Consciousness disorder C0013117 Dreaming HSDN C0042571 Vertigo subjective C3810814 Myocardial infarction ecg assessment HSDN C0042963 Symptoms vomiting C0266209 Congenital dilatation of colon MalaCards C0427055 Face weakness C3554599 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 MalaCards|UMLS C1384666 Decreased hearing C2984289 Melanoma pathway HSDN C2984058 Have pain C0031149 Peritoneal neoplasms HSDN C4084774 Have weight loss C0031212 Personality disorders HSDN C4085317 Diarrhea frequency C0334664 Mast cell neoplasm OrphaNet C1963086 Confusion adverse event C0005586 Bipolar disorder HSDN C2911645 Weight loss adverse event C0023827 Liposarcoma MalaCards C0036572 Convulsion C0242966 Systemic inflammatory response syndrome HSDN C4085211 Pain distress question C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C1549543 Administration method - pain C0014394 Enuresis HSDN C1557397 Adverse event associated with pain C0037997 Splenic diseases HSDN C0034933 Abnormal reflexes C0026764 Multiple myeloma HSDN C3887638 Failure to thrive in infant C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C0015468 Face pain C0020499 Hyperostoses, sternocostoclavicular HSDN C1971624 Appetite absent C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C0039070 Collapse fleeting C0037930 Spinal cord neoplasms HSDN C0013608 Cardiac edema C0018799 Heart diseases HSDN C0022346 Yellow skin C0006840 Candidiasis HSDN C4085317 Diarrhea frequency C0008775 Ciguatera poisoning HSDN C2919142 Short stature adverse event C0410539 Craniodiaphyseal dysplasia OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C1546654 Specimen source codes - granuloma HSDN C1963249 Tinnitus adverse event C0018801 Heart failure HSDN C0002622 Amnesias C0023895 Liver diseases HSDN C0030554 Abnormal sensation C0085682 Hypophosphatemia HSDN C1961131 Cough adverse event C0037928 Spinal cord diseases HSDN C0011991 Loose stools C0020625 Hyponatremia HSDN|UMLS C4085211 Pain distress question C0281865 Hip injury HSDN C3641756 Have diarrhea C0006285 Bronchopneumonia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003431 Antisocial personality disorder HSDN C4084773 Bothered by weight gain C0009244 Behavioral cognitive therapy HSDN C0042024 Urine incontinence C1963674 Spinocerebellar ataxia 10 MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0242875 Ventricular septal rupture HSDN C0042940 Disorder of voice C0241158 Cicatrix skin HSDN C4084725 Usual severity cough C0009373 Colonic diseases HSDN C0027066 Myoclonic jerking C0021432 Infratentorial neoplasms HSDN C0026821 Cramp C1837091 Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency MalaCards|HPO|UMLS C0042928 Paralysis vocal cord C0035242 Respiratory tract diseases HSDN C1313921 Urinomas C0006288 Bronchopulmonary sequestration HSDN C0036572 Convulsion C0030500 Animal parasitic disease HSDN C0013604 Edematous C0017665 Membranous glomerulonephritis HSDN C2984058 Have pain C0009443 Common cold HSDN C0557874 Global developmental delay C1864827 Holoprosencephaly 5 HPO C0020615 Hypoglycemia nos C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0030486 Extremity paralysis, lower C0268407 Senile cardiac amyloidosis MalaCards C0022346 Yellow skin C0000771 Abnormalities, drug induced HSDN C2198882 Disturbing or unusual thoughts, feelings, or sensations C0011253 Delusions UMLS C0036572 Convulsion C0029458 Osteoporosis, postmenopausal HSDN C0036572 Convulsion C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C2029884 Hearing loss by exam C0009324 Ulcerative colitis HSDN C0037384 Snore C0027051 Myocardial infarction HSDN C4084802 Usual severity diarrhea C0021308 Infarction HSDN C4084725 Usual severity cough C0010340 Critical illness HSDN C3829611 Nausea frequency C0027902 Neuropsychological diagnosis HSDN C0015300 Ocular proptosis C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C4084726 Distress cough C0015230 Exanthema HSDN C0011570 Monopolar depression C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0476273 Distress respiratory C1299608 Respiratory tract infection acute transient distress with sepsis UMLS C0036572 Convulsion C1852576 Copper deficiency, familial benign OrphaNet|MalaCards C0242936 Center pain C0009663 Condylomata acuminata HSDN C2984058 Have pain C3489413 Lipomatosis, multiple HSDN C0007758 Cerebellar ataxia C0007760 Cerebellar diseases UMLS C2242996 Tingling C0270617 Adhesive arachnoiditis OrphaNet|MalaCards C3463815 Feel fatigue C0007222 Cardiovascular diseases HSDN C0011168 Disorder deglutition C3250443 Myotonic dystrophy 1 MalaCards C4085642 Level of joint stiffness C4024961 Metachromatic leukodystrophy variant MalaCards C0007166 Cardiac output decreased C0162872 Aortic aneurysm, thoracic HSDN C4084767 Bothered by vomiting C0010674 Cystic fibrosis HSDN C1963252 Tremor adverse event C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating HSDN C4085661 Usual severity nausea C0022658 Kidney diseases HSDN C2203646 Jaundice C0042373 Vascular diseases HSDN C0424755 Fever symptoms C1384665 Hfe gene HSDN C0424755 Fever symptoms C0950123 Inborn genetic disease HSDN C0037383 Sneeze C0042783 Visceral prolapse HSDN C1549543 Administration method - pain C0009953 Convulsive therapy HSDN C0042024 Urine incontinence C0037397 Behavior social HSDN C0518090 Frequency of pain question C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C2024893 Cardiovascular surgery result: fatigue C0563150 Catastrophization HSDN C0015468 Face pain C0015379 Extravasation of diagnostic and therapeutic materials HSDN C0424755 Fever symptoms C0023055 Laryngeal neoplasm HSDN C2315100 Pediatric failure to thrive C3279793 Combined oxidative phosphorylation deficiency 8 MalaCards C0042798 Vision dim C3150715 Retinitis pigmentosa 51 MalaCards|HPO C0036572 Convulsion C0009187 Coccidiosis HSDN C0013595 Eczematous dermatitis C1846059 Roifman syndrome MalaCards C0426579 Anorexia symptom C0079504 Hermanski-pudlak syndrome MalaCards C0030486 Extremity paralysis, lower C0007099 Carcinoma in situ HSDN C3887873 Hearing loss C0016508 Congenital foot deformity HSDN C0018784 Deafness sensorineural C0027726 Nephrotic syndrome HSDN C0027066 Myoclonic jerking C2984572 Malaria pathway HSDN C0036572 Convulsion C0041473 Camp fever HSDN C0002170 Alopecia disorders C2931404 Albright's hereditary osteodystrophy MalaCards C0012833 Dizzy C0395903 Mastoiditis acute with labyrinthitis UMLS C0007642 Cellulitis nos C0406645 Amyopathic dermatomyositis MalaCards C0036572 Convulsion C3888385 Peroxisome biogenesis disorder 7a (zellweger) MalaCards C0557874 Global developmental delay C0270855 Early myoclonic encephalopathy OrphaNet|HPO|MalaCards C2029884 Hearing loss by exam C1861923 Acampomelic campomelic dysplasia MalaCards C0151798 Liver necrosis C0334299 Carcinoid tumor no icd-o subtype MalaCards C0242936 Center pain C0036093 Salivary gland diseases HSDN C3829611 Nausea frequency C1861848 Paragangliomas 4 MalaCards C0043068 Friderichsen-waterhouse syndrome C0011071 Sudden death HSDN C0011991 Loose stools C0042995 Vulvar neoplasms HSDN C0030193 Sense of pain C0423712 Iliohypogastric nerve neuralgia UMLS C0036572 Convulsion C1855033 Mitochondrial myopathy with lactic acidosis OrphaNet|MalaCards C0003811 Cardiac rhythm disturbance C3553529 Combined oxidative phosphorylation deficiency 10 MalaCards C0522224 Palsied C0026782 Mumps vaccine HSDN C0005745 Blepharoptosis C0079299 Epidermolysis bullosa simplex kobner OrphaNet|HPO C0000737 Abdomen pain C0862981 Resectable cholangiocarcinoma UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C0206093 Neuroectodermal tumors HSDN C4085862 Bothered by nausea C0037744 Perceptual spatial orientation HSDN C2096293 Ent surgical result ear vertigo C0026780 Mumps HSDN C1557397 Adverse event associated with pain C0206692 Carcinoma, lobular HSDN C4085642 Level of joint stiffness C0085261 Proteus syndrome HPO C0014591 Bleeding nose C1861194 Thrombasthenia-thrombocytopenia, hereditary MalaCards|HPO C0476273 Distress respiratory C0035220 Respiratory distress syndrome, newborn MalaCards|UMLS C0004134 Dyssynergia C0453996 Tobacco smoking HSDN C4084802 Usual severity diarrhea C0025517 Metabolic diseases HSDN C1549543 Administration method - pain C0002992 Angiomatosis HSDN C2024893 Cardiovascular surgery result: fatigue C0023176 Lead poisoning HSDN C4084788 Have dizziness C0030318 Panic state HSDN C0497406 Over weight C0517555 Venous thrombosis after immobility HSDN C1963281 Vomiting adverse event C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C2984058 Have pain C0024312 Lymphopenia HSDN C0036572 Convulsion C1096902 Infantile sialic acid storage disease MalaCards|HPO|UMLS C0013604 Edematous C0751422 Hereditary autoinflammatory diseases HSDN C1963184 Nystagmus adverse event C3553937 Pbd4b MalaCards C0518090 Frequency of pain question C0003504 Aortic valve insufficiency HSDN C0030193 Sense of pain C0085433 Acquired joint deformities HSDN C1959630 Eye pain adverse event C0042162 Uveal neoplasms HSDN C1384666 Decreased hearing C0752166 Bardet-biedl syndrome MalaCards|HPO C0007758 Cerebellar ataxia C0751843 Aca infarction HSDN C0035229 Respiratory function impaired C0020681 Sleep-related respiratory failure MalaCards C0036572 Convulsion C2720434 Macroencephaly HSDN C1963071 Back pain adverse event C1704436 Peripheral arterial diseases HSDN C4084775 Usual severity weight loss C0021280 Infant nutrition disorder HSDN C0349588 Stature short C1832111 Dyssegmental dysplasia with glaucoma MalaCards C0030975 Disorders perception C0149931 Migraine disorders HSDN C0005745 Blepharoptosis C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0043094 Weight gain C0085183 Neoplasms, second primary HSDN C0020538 Hbp C1842247 Coronary artery disease, autosomal dominant, 1 MalaCards C1963170 Hypothermia adverse event C0238015 Autonomic dysreflexia HSDN C3665492 Pigmentations C0154893 Hereditary choroid dystr. nos MalaCards C0917816 Deficiency mental C1846170 Mental retardation, x-linked, syndromic 7 OrphaNet|MalaCards C1557397 Adverse event associated with pain C0005683 Urinary bladder calculi (disorder) HSDN C3146279 Coma C0236969 Substance-related disorders HSDN C0007859 Pain neck C0014860 Perforation esophagus HSDN C0233514 Behavior abnormal C0751706 Primary progressive nonfluent aphasia MalaCards C0026821 Cramp C0011993 Vipoma OrphaNet|MalaCards C4085211 Pain distress question C0025364 Mental status schedule HSDN C0085642 Asphyxia reticularis C0033300 Progeria HSDN C4085210 Usual severity pain C0035008 Reinforcement schedules HSDN C2984058 Have pain C0030920 Peptic ulcer HSDN C0022346 Yellow skin C3150343 Hemolytic anemia, nonspherocytic, due to hexokinase deficiency HPO|UMLS C0037316 Not enough sleeping C0032285 Pneumonia HSDN C2188545 Anuria C1856143 Hemolytic uremic syndrome, typical MalaCards C4084802 Usual severity diarrhea C0010308 Congenital hypothyroidism HSDN C3898969 Have been vomiting C3814778 Hemolytic index HSDN C0700072 Encounter due to stillbirth C1848599 Vacterl association with hydrocephalus HPO C0857305 Thrombocytopenia purpura C0017658 Glomerulonephritis HSDN C0009676 Confusion state C0025289 Meningitis HSDN C4085548 Usual severity dizziness C0015802 Femur fracture HSDN C0018524 Hallucinate C0796561 Melanoma vaccines HSDN C2984058 Have pain C0596775 Behavior information seeking HSDN C3178766 Nociceptive pain C0206139 Lichen planus, oral HSDN C0151786 Weakness muscle C0033054 Prenatal exposure delayed effects HSDN C0851578 Disorder sleep C0018798 Congenital heart defects HSDN C0036572 Convulsion C3279716 Hypoacetylaspartia MalaCards C3539890 Pelvic pain causes awakening at night C0018199 Granuloma, plasma cell HSDN C2911647 Weight gain adverse event C0001349 Acute-phase reaction HSDN C3641756 Have diarrhea C0024305 Lymphoma, non-hodgkin HSDN C0086437 Joint hypermobility C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C0023012 Delay language C1846055 Siderius x-linked mental retardation syndrome MalaCards C1557397 Adverse event associated with pain C0006266 Bronchial spasm HSDN C0003467 Angst C1970035 Parkinson disease 6, late-onset, susceptibility to HPO C0233565 Bradykinesia C1836694 Striatal degeneration, autosomal dominant OrphaNet|HPO|UMLS C0015799 Feminisation C0949595 Gonadal dysgenesis, 46,xx HSDN C4084768 Usual severity vomiting C1563705 Nephrogenic diabetes insipidus, type i HPO C1838869 Proximal neurogenic muscle weakness C1863599 Hereditary myopathy with early respiratory failure HPO C0000737 Abdomen pain C0019911 Hookworm infections MalaCards C0018780 Frequencies hearing high loss C0243025 Hantavirus pulmonary syndrome HSDN C0005779 Clotting C0085605 Liver failure MalaCards C0026821 Cramp C1962979 Burn adverse event HSDN C0042024 Urine incontinence C0020550 Hyperthyroidism HSDN C0557874 Global developmental delay C3150787 Chromosome 17q21.31 duplication syndrome MalaCards C4085548 Usual severity dizziness C0428953 Ecg infarction myocardial HSDN C0851578 Disorder sleep C0001889 Akinetic mutism HSDN C4084724 Usual severity constipation C0085092 Parenting behavior HSDN C0522224 Palsied C0334142 Ischaemic contracture HSDN C1962972 Proteinuria adverse event C0007124 Noninfiltrating intraductal carcinoma HSDN C0015799 Feminisation C0032002 Pituitary diseases HSDN C0270948 Neurogenic muscular atrophy C0015624 Fanconi syndrome HPO C0349588 Stature short C3469605 Pseudohypoaldosteronism, type iid MalaCards C4084768 Usual severity vomiting C0032851 Disease poultry HSDN C0018681 Headache, cephalalgia C0003850 Arteriosclerosis HSDN C2032396 Pelvic pain on the right C0563150 Catastrophization HSDN C4085317 Diarrhea frequency C0037929 Spinal cord injuries HSDN C0018681 Headache, cephalalgia C1621958 Glioblastoma multiforme MalaCards C0009421 Comatose C0018799 Heart diseases HSDN C0012833 Dizzy C0025284 Meningeal neoplasms HSDN C1963065 Apnea adverse event C0005586 Bipolar disorder HSDN C1145670 Failure respiratory C3714932 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 MalaCards C3463815 Feel fatigue C0029882 Otitis media HSDN C0002965 Crescendo angina C0007193 Cardiomyopathy, dilated HSDN C0033774 Skin pruritus C0007137 Squamous cell carcinoma HSDN C0041657 Consciousness loss C0021843 Intestinal obstruction HSDN C0043094 Weight gain C0026764 Multiple myeloma HSDN C0020455 Hypergammaglobulinemia C2350476 Myositis orbital HSDN C0007758 Cerebellar ataxia C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO|UMLS C0231807 Dyspnea exertional C0268237 Cytochrome-c oxidase deficiency MalaCards|HPO|UMLS C0424755 Fever symptoms C0011853 Diabetes mellitus, experimental HSDN C0700078 Deep tendon reflex decrease C2751831 Myopathy, myofibrillar, bag3-related MalaCards|HPO C0018777 Deafness, conductive C0206672 Eccrine hidrocystoma HSDN C0869256 Urge and stress incontinence C0810038 Genitourinary symptoms and ill-defined conditions UMLS C0042928 Paralysis vocal cord C4050613 Anxiety scale (basc-2) HSDN C2984057 Have nausea C0032965 Pregnancy complications, infectious HSDN C0030193 Sense of pain C1456865 Ureteral calculi HSDN C3539895 Pelvic pain occurs with bowel movement C0042341 Varicocele HSDN C1069915 Vertigo C0031090 Periodontal diseases HSDN C0013390 Cramps menstrual C0009862 Contraception behavior HSDN C0034150 Skin purpura C0007781 Intracranial embolism and thrombosis HSDN C4085317 Diarrhea frequency C0085073 Prosthesis-related infection HSDN C1279888 Proteinuria of undiagnosed cause C0032227 Pleural effusion disorder HSDN C0728710 Pupil constriction observed C1565107 Disorder, secondary headache HSDN C0413252 Hypothermia due to exposure C0041466 Typhoid fever HSDN C0005745 Blepharoptosis C1443901 Intestinal botulism OrphaNet|MalaCards C4084725 Usual severity cough C0004935 Animal ethology HSDN C4084768 Usual severity vomiting C1962958 Hematoma adverse event HSDN C1557397 Adverse event associated with pain C0033968 Psychotherapeutic technique HSDN C0339250 Melanin pigmentation of cornea C0162281 Corneal deposit UMLS C0413252 Hypothermia due to exposure C0242698 Ventricular dysfunction, left HSDN C0040264 Ear ringing sound C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0042755 Virilisation C4085311 Depression - recess HSDN C0151786 Weakness muscle C0006264 Bronchial neoplasms HSDN C1963087 Constipation adverse event C0007820 Cerebrovascular disorders HSDN C0026826 High muscle tone C2930913 Chromosome 13q deletion MalaCards C0235777 Neonatal cyanosis C1285537 Neonatal cardiovascular disorder UMLS C0851578 Disorder sleep C0006840 Candidiasis HSDN C0026838 Spasticity muscle C0265227 Schinzel-giedion syndrome UMLS C0241210 Speaking delay C1845902 Fg syndrome 2 MalaCards|HPO C1557397 Adverse event associated with pain C0027438 Nasopharynx HSDN C2024893 Cardiovascular surgery result: fatigue C0085257 Yin deficiency HSDN C1860844 Sparse, thin hair C3492944 Lentiginosis profusa MalaCards C0030200 Intractable pain C0038356 Stomach neoplasms HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0033968 Psychotherapeutic technique HSDN C1384666 Decreased hearing C1522133 High cholesterol level HSDN C2984057 Have nausea C0042338 Herpesvirus 3, human HSDN C0013604 Edematous C0010417 Cryptorchidism HSDN C0042514 Ventricular tachycardia C1834481 Cardiomyopathy, dilated, 1s MalaCards C0026821 Cramp C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0030552 Paralysis partial C0305062 Tetanus toxoids HSDN C0000737 Abdomen pain C1527429 Increased blood npn HSDN C1963091 Diarrhea adverse event C0020877 Ileitis DiseaseOntology|MalaCards C0013378 Dysgensia C0006271 Bronchiolitis HSDN C0003862 Pain joint C0263666 Dermatomyositis, childhood type OrphaNet|MalaCards C4084802 Usual severity diarrhea C0043398 Yellow fever, urban MalaCards C0002962 Angina C0038016 Spondylolisthesis HSDN C4084774 Have weight loss C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C0037286 Skin neoplasms HSDN C0030232 Color loss C1858990 Beta thalassemia, dominant inclusion body type OrphaNet|HPO C0027497 Queasy C0013274 Patent ductus arteriosus HSDN C4084768 Usual severity vomiting C0556346 Binge drinking HSDN C0016382 Cutaneous vascular engorgement C0011608 Dermatitis herpetiformis OrphaNet|MalaCards C4085317 Diarrhea frequency C0029182 Orbit (eye disorders) HSDN C1963093 Dizziness adverse event C0026771 Trauma multiple HSDN C1961131 Cough adverse event C0700595 Spinal muscular atrophies of childhood HSDN C0151740 Intracranial hypertension C0007795 Diffuse cerebral sclerosis of schilder MalaCards C4085661 Usual severity nausea C0006309 Brucellosis HSDN C1963170 Hypothermia adverse event C1449861 Micronuclei, chromosome-defective HSDN C0018926 Emesis bloody C1881712 Medical device material rupture HSDN C0030552 Paralysis partial C2931482 Neurofibromatosis-noonan syndrome MalaCards|HPO C0237326 Defecation pain C3809877 Schaaf-yang syndrome MalaCards C0349588 Stature short C1839874 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis HPO C3539023 Pelvic pain increasing in frequency C2984291 Glioblastoma multiforme pathway HSDN C3641755 Have constipation C0019372 Herpesviridae infections HSDN C0036572 Convulsion C0585442 Osteosarcoma of bone HSDN C0027066 Myoclonic jerking C3698239 Cerebral cortex myoclonus UMLS C1962972 Proteinuria adverse event C1567741 Alport syndrome OrphaNet C1963086 Confusion adverse event C0314657 Genetic predisposition HSDN C0750319 Vomit appearance coffee ground C0162651 Gastric outlet obstruction UMLS C0020673 Hypothermia (central) (local) C0005586 Bipolar disorder HSDN C2242996 Tingling C0004096 Asthma HSDN C0019825 Voice hoarseness C0039978 Thoracic diseases HSDN C0013604 Edematous C0004352 Autistic disorder HSDN C3898969 Have been vomiting C0004352 Autistic disorder HSDN C0043144 Wheeze C0006287 Bronchopulmonary dysplasia MalaCards C4085210 Usual severity pain C0027868 Neuromuscular diseases HSDN C2984057 Have nausea C1555914 Psychologist - psychotherapy, group HSDN C0026205 Pupillary constriction C0700359 Organophosphate poisoning HSDN C0085631 Abnormal excitement C0453996 Tobacco smoking HSDN C3274924 Have been coughing C0003850 Arteriosclerosis HSDN C0006370 Bulimia C0007222 Cardiovascular diseases HSDN C1557397 Adverse event associated with pain C0007684 Central nervous system infection HSDN C1963170 Hypothermia adverse event C0262655 Recurrent urinary tract infection HSDN C4085210 Usual severity pain C0002949 Aneurysm, dissecting HSDN C0030193 Sense of pain C0162557 Liver failure, acute HSDN C0178417 Anhedonia C2350520 Olfactory perception HSDN C2911647 Weight gain adverse event C0079487 Helicobacter infections HSDN C0013378 Dysgensia C0038362 Stomatitis HSDN C2096293 Ent surgical result ear vertigo C0035126 Reperfusion injury HSDN C1384666 Decreased hearing C0016045 Fibroma HSDN C0231341 Aging premature C0019542 Higher nervous activity HSDN C4084768 Usual severity vomiting C0001768 Agammaglobulinemia HSDN C3203358 Alveolar hypoventilation C0238015 Autonomic dysreflexia HSDN C2911645 Weight loss adverse event C0006818 Campylobacter infection HSDN C4085317 Diarrhea frequency C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0231218 Malaise generalized C0854833 Angiocentric lymphoma stage i UMLS C4084773 Bothered by weight gain C0024305 Lymphoma, non-hodgkin HSDN C0030552 Paralysis partial C0041409 Turner syndrome, male MalaCards C0085631 Abnormal excitement C1546533 Specimen source codes - abscess HSDN C0851578 Disorder sleep C0027666 Neoplasms, radiation-induced HSDN C0042025 Urinary incontinence stress C0030567 Parkinson disease HSDN C4085211 Pain distress question C0001206 Acromegaly HSDN C0011206 Delirium acute C0038395 Streptococcal infections HSDN C4042891 Sleep wake disorders C0018802 Congestive heart failure HSDN C4084775 Usual severity weight loss C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C0027796 Neuralgias C0034088 Pulmonary valve insufficiency HSDN C0009421 Comatose C0031154 Peritonitis HSDN C1557397 Adverse event associated with pain C0004509 Azoospermia HSDN C0028961 Urine output decreased C0027726 Nephrotic syndrome HSDN C0039070 Collapse fleeting C0030920 Peptic ulcer UMLS C0917816 Deficiency mental C4014738 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 MalaCards C0027066 Myoclonic jerking C0035126 Reperfusion injury HSDN C2229014 Menstrual-type cramping C0013390 Dysmenorrhea UMLS C0002962 Angina C0024143 Lupus nephritis HSDN C0232493 Epigastric pain C1997249 Neuralgia, pudendal MalaCards C4084767 Bothered by vomiting C0033953 Psychosexual disorders HSDN C0424755 Fever symptoms C0007785 Cerebral infarction HSDN C0375479 Pyrexia of unknown origin during the puerperium, postpartum condition or complication C0810050 Other complications of birth; puerperium affecting management of mother UMLS C2984058 Have pain C0003047 Animal disease HSDN C4085211 Pain distress question C0016549 Foreign body reaction HSDN C0013362 Dysarthrias C0410204 Myopathy, centronuclear, autosomal recessive HPO C0518090 Frequency of pain question C0162834 Hyperpigmentation HSDN C0039070 Collapse fleeting C0340288 Stable angina UMLS C0030193 Sense of pain C1511281 Breast adenocarcinoma with spindle cell metaplasia UMLS C0020538 Hbp C0032463 Polycythemia vera OrphaNet C0013604 Edematous C0034072 Cor pulmonale HSDN C3641756 Have diarrhea C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0595812 Fistula route HSDN C1963252 Tremor adverse event C0042870 Vitamin d deficiency HSDN C1557397 Adverse event associated with pain C0014550 Epilepsies, myoclonic HSDN C2024878 Cardiovascular surgery result: dyspnea C0151636 Premature ventricular contractions HSDN C0026821 Cramp C0242287 Isaacs syndrome OrphaNet|UMLS|HPO|MalaCards C0018784 Deafness sensorineural C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C4085317 Diarrhea frequency C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0242936 Center pain C0032788 Postoperative hemorrhage HSDN C0027497 Queasy C0018021 Goiter HSDN C0518090 Frequency of pain question C0022572 Keratoacanthoma HSDN C0023012 Delay language C1136249 Mental retardation, x-linked HPO C4085210 Usual severity pain C0034072 Cor pulmonale HSDN C0011570 Monopolar depression C0162531 Hereditary coproporphyria OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027121 Myositis HSDN C1384666 Decreased hearing C0796133 Ramon syndrome MalaCards C0413252 Hypothermia due to exposure C0027902 Neuropsychological diagnosis HSDN C2984058 Have pain C0206754 Neuroendocrine tumors HSDN C4085317 Diarrhea frequency C0342609 Hereditary oculoleptomeningeal amyloid angiopathy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0029877 Ear inflammation HSDN C0031315 Phantom limb pain C0036677 Sensory threshold HSDN C3898969 Have been vomiting C0268328 Porphobilinogen synthase deficiency MalaCards|HPO C0036572 Convulsion C1845517 Hydroxyacyl-coa dehydrogenase, type 2, deficiency HPO|UMLS C0851578 Disorder sleep C0403447 Chronic kidney insufficiency HSDN C0427285 Click hip C0810350 Non-traumatic joint disorders UMLS C0011991 Loose stools C0001857 Aids related complex UMLS C1549543 Administration method - pain C0403447 Chronic kidney insufficiency HSDN C0009676 Confusion state C0041327 Tuberculosis, pulmonary HSDN C3887638 Failure to thrive in infant C0009995 Cor triatriatum HSDN C4024610 Leg muscle stiffness C0162309 Adrenoleukodystrophy OrphaNet|MalaCards C3887784 Decreased urine output C1263960 Diabetic coma HSDN C0085602 Polydypsia C0020598 Hypocalcemia HSDN C0042571 Vertigo subjective C0033923 Psychomotor function HSDN C0004134 Dyssynergia C0751865 Alcohol-induced disorders, nervous system HSDN C0020615 Hypoglycemia nos C0268542 Ornithine carbamoyltransferase deficiency OrphaNet|HPO C0010200 Cough symptom C0019655 Histoplasmosis HSDN C1963063 Anorexia adverse event C0013124 Behavior drinking HSDN C1549543 Administration method - pain C0020651 Hypotension, orthostatic HSDN C0000737 Abdomen pain C0554114 Epstein-barr virus hepatitis MalaCards C2024878 Cardiovascular surgery result: dyspnea C0235833 Congenital diaphragmatic hernia HSDN C3641756 Have diarrhea C0037047 Sibling HSDN C1963071 Back pain adverse event C0036202 Sarcoidosis HSDN C2032395 Pelvic pain on the left C0206680 Mesothelioma, cystic HSDN C4085862 Bothered by nausea C0022661 Kidney failure, chronic HSDN C1850534 Generalized edema C0272199 Familial hemophagocytic lymphocytosis MalaCards C0029163 Hemorrhage mouth C0018920 Hemangioma, cavernous HSDN C4084774 Have weight loss C1963088 Cystitis adverse event HSDN C0518090 Frequency of pain question C0524851 Neurodegenerative disorders HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1546847 Entity name part type - family HSDN C2911647 Weight gain adverse event C0026266 Mitral valve insufficiency HSDN C0036572 Convulsion C2936349 Plaque, amyloid HSDN C1963093 Dizziness adverse event C2984572 Malaria pathway HSDN C0040034 Thrombocytopenia C0001768 Agammaglobulinemia MalaCards C0232726 Tenesmus, rectal C0002986 Fabry disease MalaCards|HPO|UMLS C0018681 Headache, cephalalgia C1401747 Quadrilateral fever MalaCards C0086565 Liver function abnormal C3808991 Congenital disorder of deglycosylation MalaCards C2984058 Have pain C0043255 Stab wound HSDN C4085211 Pain distress question C0026590 Child mother relationship HSDN C4085548 Usual severity dizziness C0003469 Anxiety disorders HSDN C3539896 Pelvic pain occurs with urination C0282606 Myomatous neoplasm HSDN C0020673 Hypothermia (central) (local) C1457883 Aggressive reaction HSDN C3463815 Feel fatigue C0016977 Gall bladder diseases HSDN C0004604 Pain back C0031511 Pheochromocytoma HSDN C3251821 Reaction catatonic C0007398 Catatonia UMLS C1963252 Tremor adverse event C1876175 Ataxia-telangiectasia variant MalaCards|HPO C0030552 Paralysis partial C0024228 Lymphatic diseases HSDN C3539891 Pelvic pain to the rear C2706915 Language:-:point in time:^patient:- HSDN C0013390 Cramps menstrual C0017416 Genital neoplasms, female HSDN C0036396 Sciatica C0041296 Tuberculosis HSDN C0030552 Paralysis partial C0006109 Brain damage, chronic HSDN C0036659 Sensation disorder C0027659 Neoplasms, experimental HSDN C0150055 Pain chronic C0022758 Kap HSDN C0011991 Loose stools C3809369 Paroxysmal nocturnal hemoglobinuria 2 MalaCards|UMLS C0917801 Sleep disorder insomnia C0022336 Creutzfeldt-jakob disease MalaCards C0917816 Deficiency mental C2931119 Mehes syndrome OrphaNet|MalaCards C0018991 Paralysis one side of body C1457883 Aggressive reaction HSDN C0007398 Catatonic C0037952 Spinocerebellar degeneration HSDN C0151827 Pain eye C0155305 Optic neuropathy, ischemic HSDN C0020578 Hyperventilate C0024530 Malaria HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1963198 Pancreatitis adverse event HSDN C4084776 Weight loss C0162820 Dermatitis, allergic contact HSDN C0042571 Vertigo subjective C0014852 Esophageal diseases HSDN C0036396 Sciatica C0037274 Dermatologic disorders HSDN C0018772 Deafness C0265493 Cat eye syndrome MalaCards C2984058 Have pain C1527311 Brain edema HSDN C3146279 Coma C0013870 Electroconvulsive shock HSDN C1963274 Vasculitis adverse event C0410422 Chronic multifocal osteomyelitis MalaCards C0019079 Bloody sputum C1999266 Depression adverse event HSDN C0004604 Pain back C0041755 Adverse reaction to drug HSDN C0036572 Convulsion C1865349 Ethylmalonic encephalopathy HPO|UMLS C0184567 Pain acute C0017924 Glycogen storage disease type v HSDN C1549543 Administration method - pain C2936490 Cardiac arrest, out-of-hospital HSDN C0518090 Frequency of pain question C0021295 Infant, premature, diseases HSDN C3163620 Hypotension adverse event C0270726 Alexander disease OrphaNet|MalaCards C0043094 Weight gain C0010633 Cystadenoma HSDN C4084788 Have dizziness C0034494 Rabies (disorder) HSDN C0018784 Deafness sensorineural C0085605 Liver failure MalaCards C1963281 Vomiting adverse event C0039730 Thalassemia HSDN C0427068 Legs weakness C0025284 Meningeal neoplasms MalaCards C0042571 Vertigo subjective C0271490 Diffuse labyrinthitis UMLS C1963087 Constipation adverse event C0020456 Hyperglycemia HSDN C0007758 Cerebellar ataxia C0003076 Aniridia HSDN C0424755 Fever symptoms C1299262 Sarcoma - category (morphologic abnormality) HSDN C2032395 Pelvic pain on the left C0000768 Congenital abnormality HSDN C3463815 Feel fatigue C0001403 Addison disease OrphaNet C0005745 Blepharoptosis C0796059 Oculopalatoskeletal syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0017570 Gingival neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0041296 Tuberculosis OrphaNet|HPO C0242936 Center pain C0024523 Malabsorption syndrome HSDN C0019521 Hiccoughs C0085315 Toxoplasmosis, cerebral HSDN C0857305 Thrombocytopenia purpura C0517555 Venous thrombosis after immobility HSDN C0011175 Deficient fluid volume C1846344 Bartter syndrome, type 3, with hypocalciuria HPO C4084724 Usual severity constipation C2911243 Encounter due to family history of colonic polyps HSDN C1384666 Decreased hearing C0003850 Arteriosclerosis HSDN C3665347 Vision impaired C1857395 De toni-debre-fanconi syndrome HPO C1963281 Vomiting adverse event C0162872 Aortic aneurysm, thoracic HSDN C3641756 Have diarrhea C0007766 Intracranial aneurysm HSDN C0426579 Anorexia symptom C0854795 Resectable hepatic malignant neoplasm MalaCards C0042798 Vision dim C1963198 Pancreatitis adverse event HSDN C4085548 Usual severity dizziness C1142166 Brugada syndrome (disorder) HSDN C4084766 Vomiting C0014170 Endometrial neoplasms HSDN C0151908 Dry skin C0406767 Keratoderma with scleroatrophy of the extremities OrphaNet|MalaCards C3641756 Have diarrhea C0042138 Uterine neoplasms HSDN C1557397 Adverse event associated with pain C0005747 Blepharospasm HSDN C1963064 Anxiety adverse event C1846058 Lubs x-linked mental retardation syndrome HPO C0426579 Anorexia symptom C0029340 Orthomolecular therapy HSDN C4084727 Cough frequency C0860603 Anxiety symptoms HSDN C1963087 Constipation adverse event C0037928 Spinal cord diseases HSDN C0010038 Corneal opacity disorder C0344559 Irido-corneo-trabecular dysgenesis (disorder) HPO C0011991 Loose stools C1548777 Specimen reject reason - hemolysis HSDN C3641756 Have diarrhea C0267662 Congenital chloride diarrhea MalaCards|HPO C0497406 Over weight C0206171 Community acquired infections HSDN C4084768 Usual severity vomiting C1532560 Plasmacytoma - category HSDN C0349588 Stature short C0432197 Short rib-polydactyly syndrome, verma-naumoff type MalaCards C0018772 Deafness C0010273 Craniofacial dysostosis HSDN|HPO C0036572 Convulsion C0030409 Paracoccidioidomycosis HSDN C2984057 Have nausea C0268647 Lysinuric protein intolerance MalaCards|HPO C1961131 Cough adverse event C0001261 Actinomycosis HSDN C0009792 Consciousness disorder C0012979 Canine disease HSDN C0242936 Center pain C0041956 Ureteral obstruction HSDN C4084724 Usual severity constipation C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C0009421 Comatose C0042138 Uterine neoplasms HSDN C2984058 Have pain C0008479 Chondrosarcoma HSDN C2242996 Tingling C1710146 Familial spinal arachnoiditis MalaCards C0013428 Painful urination C1517579 Infiltrating bladder urothelial carcinoma, micropapillary variant UMLS C3539889 Pelvic pain increasing in severity C0206680 Mesothelioma, cystic HSDN C3829611 Nausea frequency C1963137 Hydrocephalus adverse event HSDN C0010038 Corneal opacity disorder C0020074 Hsan type iv MalaCards C0040822 D tremors C1961835 Gaucher disease, type 1 MalaCards C0000737 Abdomen pain C0279000 Liver and intrahepatic biliary tract carcinoma MalaCards C1963071 Back pain adverse event C0233629 Thinking and speaking disturbances HSDN C0413252 Hypothermia due to exposure C0006277 Bronchitis HSDN C0851578 Disorder sleep C1556682 Adverse event associated with infection HSDN C0151786 Weakness muscle C0003864 Arthritis HSDN C0085593 Chill C0242707 Ventricular dysfunction, right HSDN C0037763 Spasm C0018193 Granuloma, foreign-body HSDN C0026858 Musculoskeletal pain C0023676 Life style HSDN C0344315 Mood depressed C2751842 Parkinson disease 14, autosomal recessive MalaCards|HPO C0041834 Erythematous condition C0473546 Vibratory angio-edema MalaCards C0151825 Ostalgia C2698307 B acute lymphoblastic leukemia with t(5;14)(q31;q32); il3-igh UMLS C0013604 Edematous C2936881 Eosinophilic synovitis MalaCards C0040822 D tremors C0018799 Heart diseases HSDN C0009806 Constipate C0453996 Tobacco smoking HSDN C1971624 Appetite absent C0032914 Pre-eclampsia HSDN C4084768 Usual severity vomiting C0022658 Kidney diseases HSDN C2984058 Have pain C0013502 Echinococcosis HSDN C0518090 Frequency of pain question C0041960 Ureterocele HSDN C3815497 Cough C0264353 Bronchomalacia HSDN C4085317 Diarrhea frequency C0001618 Tumors of adrenal cortex HSDN C0033774 Skin pruritus C0030305 Pancreatitis HSDN C4084767 Bothered by vomiting C0033923 Psychomotor function HSDN C0011991 Loose stools C0268384 Familial amyloid neuropathy, portuguese type MalaCards C3641755 Have constipation C0007453 Cattle disease HSDN C1963093 Dizziness adverse event C0024141 Lupus erythematosus, systemic HSDN C4084767 Bothered by vomiting C0037005 Shoulder dislocation HSDN C4084802 Usual severity diarrhea C0023441 Leukemia, experimental HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3495422 Finding relating to sexuality and sexual activity HSDN C0026821 Cramp C1837092 Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency HPO C2911645 Weight loss adverse event C0027055 Myocardial reperfusion injury HSDN C4085210 Usual severity pain C0700359 Organophosphate poisoning HSDN C0030232 Color loss C1832592 Hernandez fragoso syndrome OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0016665 Fracture, nos with nonunion HSDN C4084769 Vomiting frequency C0009187 Coccidiosis HSDN C0042963 Symptoms vomiting C0032371 Poliomyelitis MalaCards|HSDN C0037199 Sinus infection C0751156 Fraxa syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0026718 Mucormycosis HSDN C0030193 Sense of pain C0021345 Infectious mononucleosis HSDN C0241137 Skin pallor C0027821 Syndrome effort HSDN C3898969 Have been vomiting C0021655 Insulin resistance HSDN C0232982 Complete spermatogenic arrest C0232981 Arrest of spermatogenesis UMLS C0040264 Ear ringing sound C3541306 Plasmodium measurement HSDN C1963249 Tinnitus adverse event C0024841 Matrimony, matrimonial HSDN C1557397 Adverse event associated with pain C0003855 Arteriovenous fistula HSDN C0518090 Frequency of pain question C0080178 Spina bifida HSDN C0413252 Hypothermia due to exposure C0021831 Intestinal diseases HSDN C0019572 Hairiness C2931579 Battaglia neri syndrome OrphaNet|MalaCards C0042963 Symptoms vomiting C0151620 Hypertensive encephalopathy HSDN C0018681 Headache, cephalalgia C0238154 Epidural hematoma HSDN C0042025 Urinary incontinence stress C1423541 Vangl2 gene HSDN C4085317 Diarrhea frequency C0026269 Mitral valve stenosis HSDN C4085222 Nausea C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C2132198 Abnormal blistering of the skin C0023645 Lichen planus follicularis MalaCards C2911645 Weight loss adverse event C0026771 Trauma multiple HSDN C1557397 Adverse event associated with pain C2350019 Solitary pulmonary nodule HSDN C4084788 Have dizziness C0023290 Leishmaniasis, visceral HSDN C0751251 Insomnia, secondary C0154565 Non-organic sleep disorder UMLS C3539889 Pelvic pain increasing in severity C0029436 Bone disease, disappearing HSDN C3665347 Vision impaired C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C4084766 Vomiting C0268293 Corticosterone methyl oxidase type i deficiency HPO C4084766 Vomiting C0023066 Laryngismus HSDN C0242936 Center pain C0043541 Zygomycoses HSDN C0009792 Consciousness disorder C0011265 Presenile dementia HSDN C3641755 Have constipation C0009475 Community mental health service HSDN C0002962 Angina C1548777 Specimen reject reason - hemolysis HSDN C0043094 Weight gain C0028738 Nystagmus HSDN C0349588 Stature short C3146244 Alcohol related birth defect OrphaNet|MalaCards C0009421 Comatose C0027080 Myoglobinuria HSDN C0239783 Groin pain C0748758 Skin cancer malignant melanoma metastatic UMLS C0270948 Neurogenic muscular atrophy C0017926 Glycogen storage disease type vii OrphaNet|HPO|MalaCards C1279511 Malarial pigment deposition C0745283 Infectious process UMLS C0012569 Double vision C0023267 Fibroid tumor HSDN C0349506 Sun sensitivity C0282644 Smith-lemli-opitz syndrome, type ii MalaCards C3539022 Pelvic pain decreasing in severity C0026857 Musculoskeletal diseases HSDN C2911645 Weight loss adverse event C1854336 Paragangliomas 3 MalaCards C0085631 Abnormal excitement C1706377 Memory device component HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029184 Orbital fracture HSDN C0016199 Pain flank C0022680 Polycystic kidney diseases HSDN C0020673 Hypothermia (central) (local) C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0015672 Decreased energy C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C4084767 Bothered by vomiting C1563215 Powassan encephalitis virus infection MalaCards C0007166 Cardiac output decreased C0021655 Insulin resistance HSDN C0002962 Angina C1963067 Atrial fibrillation adverse event HSDN C0009792 Consciousness disorder C0041296 Tuberculosis HSDN C0007758 Cerebellar ataxia C0796123 Cataract-ataxia-deafness-retardation syndrome OrphaNet|MalaCards C0019521 Hiccoughs C0037998 Splenic infarction HSDN C0015672 Decreased energy C0009373 Colonic diseases HSDN C0234428 Consciousness disturbance C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0700078 Deep tendon reflex decrease C2751312 Bartter syndrome, type 4b HPO C0023530 Leukopenia C0220748 Cartilage-hair hypoplasia OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3889576 Euphoria HSDN C2242996 Tingling C0014556 Epilepsy, temporal lobe HSDN C0019209 Large liver C0268263 Multiple sulfatase deficiency disease OrphaNet|HPO|MalaCards C0040485 Wryneck C0000833 Abscess HSDN C2096293 Ent surgical result ear vertigo C1145670 Respiratory failure HSDN C0428977 Pulse rate decrease C0749420 Thyroid agenesis HPO C0004134 Dyssynergia C0027627 Neoplasm metastasis HSDN C1962972 Proteinuria adverse event C0079631 Interdisciplinary communication HSDN C0851578 Disorder sleep C2984291 Glioblastoma multiforme pathway HSDN C0151889 Reflexes tendon increased C0014550 Epilepsies, myoclonic MalaCards C0043094 Weight gain C0038587 Substance withdrawal syndrome HSDN C0042420 Vasovagal episode C0042514 Tachycardia, ventricular HSDN C0577560 Eye mass C0431456 Congenital cysts post.segment UMLS C2315100 Pediatric failure to thrive C2931246 Chromosome 17, trisomy 17p11 2 OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0040584 Tracheitis HSDN C4084775 Usual severity weight loss C0008925 Cleft palate HSDN C0000737 Abdomen pain C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0039870 Leanness C0162316 Iron deficiency anemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018671 Head and neck neoplasms HSDN C0036572 Convulsion C0015459 Face injury HSDN C2984058 Have pain C0016989 Galvanic skin response HSDN C0497406 Over weight C0242231 Coronary stenosis HSDN C4085210 Usual severity pain C0276275 Disease due to parvoviridae HSDN C1963281 Vomiting adverse event C0342859 Harderoporphyria HPO C4084788 Have dizziness C0017638 Glioma HSDN C2919142 Short stature adverse event C0432328 Xeroderma pigmentosum, variant form MalaCards C2029884 Hearing loss by exam C0032273 Pneumoconiosis HSDN C4084769 Vomiting frequency C0008354 Cholera HSDN C2096293 Ent surgical result ear vertigo C2973725 Pulmonary arterial hypertension OrphaNet C1263846 Attention deficit disorder with hyperactivity C1096902 Infantile sialic acid storage disease MalaCards C3665386 Abnormal vision C2020284 Stickler syndrome, type 1 MalaCards|HPO C0231528 Muscle pain generalized C2873856 Essential cryoglobulinemia MalaCards C0007814 Cerebrospinal fluid otorrhea C0024221 Lymphangioma HSDN C0151908 Dry skin C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards|HPO|UMLS C4084775 Usual severity weight loss C0035222 Respiratory distress syndrome, adult HSDN C0018681 Headache, cephalalgia C0036357 Psychology, schizophrenic HSDN C3541349 Syncope C4049644 Depression HSDN C0036572 Convulsion C0002878 Anemia, hemolytic HSDN C0013362 Dysarthrias C0393547 Bulbospinal neuronopathy OrphaNet|HPO C0018681 Headache, cephalalgia C0001529 Dercum disease MalaCards C0042024 Urine incontinence C0342728 3-methylglutaconic aciduria type 1 MalaCards C0020673 Hypothermia (central) (local) C0001430 Adenoma HSDN C0036572 Convulsion C0032371 Poliomyelitis HSDN C0013604 Edematous C0026948 Mycosis fungoides MalaCards C0023014 Developmental disorder language C0028758 Bonding HSDN C0242936 Center pain C0001349 Acute-phase reaction HSDN C4085222 Nausea C0020523 Immediate hypersensitivity HSDN C0018681 Headache, cephalalgia C0278599 Cns tumor, childhood infratentorial ependymoma UMLS C0018772 Deafness C0018939 Hematological disease HSDN C0027066 Myoclonic jerking C0242422 Parkinsonian disorders HSDN C0028738 Nystagmus C2749049 Corneal dystrophy, endothelial, x-linked MalaCards C1963252 Tremor adverse event C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C1999266 Depression adverse event C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C0575081 Abnormal gait C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy HPO C0426579 Anorexia symptom C0002986 Fabry disease OrphaNet|HPO|MalaCards C4084774 Have weight loss C0268581 Holocarboxylase synthetase deficiency OrphaNet|HPO|MalaCards C0557874 Global developmental delay C1832438 Chitty hall baraitser syndrome OrphaNet|MalaCards C0242936 Center pain C0009938 Bruising HSDN C4084784 Diarrhea C2062326 Eosinophilic enteropathy OrphaNet|MalaCards C0013404 Respiratory difficulty C4050613 Anxiety scale (basc-2) HSDN C4085641 Level of joint pain C0019196 Hepatitis c DiseaseOntology|MalaCards C0020673 Hypothermia (central) (local) C0004275 Attitude health HSDN C0086439 Activity decreased C0018802 Congestive heart failure HSDN C0018772 Deafness C0022904 Lacrimal apparatus diseases HSDN C4084767 Bothered by vomiting C0008354 Cholera HSDN C0039870 Leanness C0023903 Liver neoplasms HSDN C0013404 Respiratory difficulty C1868684 Ear, patella, short stature syndrome MalaCards C4084802 Usual severity diarrhea C1834211 Ganglioneuromatosis of the alimentary tract HPO C0011991 Loose stools C0030319 Panic disorder HSDN C0013362 Dysarthrias C0394007 Atonic cerebral palsy MalaCards C4084768 Usual severity vomiting C0018552 Hamartoma HSDN C1963093 Dizziness adverse event C0003493 Aortic diseases HSDN C0036572 Convulsion C3809872 Periventricular nodular heterotopia 6 MalaCards|UMLS C0497247 Blood pressure elevation C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|HPO|MalaCards C0036572 Convulsion C0393727 Toothbrushing epilepsy UMLS C0022346 Yellow skin C0520946 Emotional hypersensitivity HSDN C2911647 Weight gain adverse event C0006736 Body stone HSDN C1961131 Cough adverse event C3714644 Thymus neoplasms OrphaNet|MalaCards C2984057 Have nausea C1706377 Memory device component HSDN C3898969 Have been vomiting C0030567 Parkinson disease HSDN C4084802 Usual severity diarrhea C0314719 Dryness of eye HSDN C0011206 Delirium acute C0007134 Renal cell carcinoma HSDN C0857102 Feeling of intense apprehension C0003467 Anxiety UMLS C0012569 Double vision C1527231 Adrenomyeloneuropathy MalaCards C2242996 Tingling C3809243 Hypocalcemia, autosomal dominant 2 MalaCards C3887638 Failure to thrive in infant C3809526 Combined oxidative phosphorylation deficiency 17 MalaCards C0023015 Language handicap C0023138 Laurence-moon syndrome HSDN C1549543 Administration method - pain C0085094 Head injury closed HSDN C4085222 Nausea C0010709 Cyst HSDN C0030197 Orbital region; pain C1400948 Infraorbital; pain UMLS C1963091 Diarrhea adverse event C0152101 Hypoplastic left heart syndrome HSDN C4084776 Weight loss C4041080 Neurocognitive disorders HSDN C0018777 Deafness, conductive C0265257 Genee-wiedemann syndrome OrphaNet|HPO C0015970 Fever unknown origin C0002395 Alzheimer's disease HSDN C1557397 Adverse event associated with pain C1302808 Myopericytoma HSDN C0039070 Collapse fleeting C1546847 Entity name part type - family HSDN C1963093 Dizziness adverse event C0752143 Intracranial thrombosis HSDN C0232536 Bolus impaction C0333124 Impaction UMLS C0042963 Symptoms vomiting C0006736 Body stone HSDN C0231528 Muscle pain generalized C0016627 Avian influenza DiseaseOntology|MalaCards C0085636 Light sensitivity C0007965 Chediak-higashi syndrome OrphaNet|HSDN|UMLS|HPO|MalaCards C0857305 Thrombocytopenia purpura C0042134 Uterine hemorrhage HSDN C4084776 Weight loss C0035309 Retinal diseases HSDN C0007758 Cerebellar ataxia C1848201 Subcortical band heterotopia HPO C2024878 Cardiovascular surgery result: dyspnea C0007192 Cardiomyopathy, alcoholic HSDN C0041657 Consciousness loss C0025309 Meningoencephalitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0010417 Cryptorchidism HSDN C3887873 Hearing loss C0051981 Anti-leprosy vaccine HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0014544 Epilepsy HSDN C0034150 Skin purpura C2873856 Essential cryoglobulinemia MalaCards C0010200 Cough symptom C0030305 Pancreatitis HSDN C2096293 Ent surgical result ear vertigo C0030319 Panic disorder HSDN C1557397 Adverse event associated with pain C0281865 Hip injury HSDN C4084768 Usual severity vomiting C0006261 Bronchial diseases HSDN C0221263 Cafe au lait spot C1854540 Carney complex, type 2 MalaCards C0033774 Skin pruritus C2911643 Encounter due to family history of osteoporosis HSDN C0002965 Crescendo angina C0206255 Malaria vaccine HSDN C0033774 Skin pruritus C0037650 Somatoform disorder HSDN C0020649 Blood pressure decreased C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C4084784 Diarrhea C0085084 Motor neuron disease HSDN C3274924 Have been coughing C0867389 Chronic graft-versus-host disease MalaCards C0043094 Weight gain C0079744 Diffuse large b-cell lymphoma HSDN C0030232 Color loss C0085576 Iron-refractory iron deficiency anemia OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0013926 Aeroembolism HSDN C1963063 Anorexia adverse event C0085655 Polymyositis OrphaNet|MalaCards C0518090 Frequency of pain question C1334928 Necrotic changes (finding) HSDN C0018834 Brash C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0004134 Dyssynergia C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C4084769 Vomiting frequency C4012395 Congenital disorder of glycosylation, type iy MalaCards C0000737 Abdomen pain C0085092 Parenting behavior HSDN C1579931 Depressed - symptom C1563715 Andersen syndrome HPO C3898969 Have been vomiting C0062527 Hepatitis b vaccine HSDN C0004134 Dyssynergia C1412747 Bbs2 gene HPO C0013362 Dysarthrias C1306794 Wound botulism OrphaNet|MalaCards C1069915 Vertigo C0149514 Bronchitis acute HSDN C4085317 Diarrhea frequency C0014394 Enuresis HSDN C1971624 Appetite absent C0039263 Takayasu arteritis OrphaNet|HPO|MalaCards C0234132 Pyramidal sign C0021368 Inflammation MalaCards C4084769 Vomiting frequency C0013336 Dwarfism HSDN C1959630 Eye pain adverse event C0034530 Injury radiation HSDN C0009421 Comatose C0014057 Japanese encephalitis DiseaseOntology|HSDN|MalaCards C0011206 Delirium acute C0004352 Autistic disorder HSDN C0020673 Hypothermia (central) (local) C0042830 Perception visual HSDN C1557397 Adverse event associated with pain C0085409 Polyendocrinopathies, autoimmune HSDN C0012569 Double vision C0031036 Polyarteritis nodosa HSDN C4085222 Nausea C3539923 Cdisc adas-cog - orientation summary score HSDN C2024878 Cardiovascular surgery result: dyspnea C0014547 Epilepsies, partial HSDN C0812426 Kidney problem C0403716 Renal calculus pelvis UMLS C3463815 Feel fatigue C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C4084769 Vomiting frequency C0004030 Aspergillosis HSDN C0018777 Deafness, conductive C0022661 Kidney failure, chronic HSDN C0413252 Hypothermia due to exposure C0020676 Hypothyroidism HSDN C0085602 Polydypsia C0020456 Hyperglycemia UMLS C0012833 Dizzy C0012979 Canine disease HSDN C0424755 Fever symptoms C0238198 Gastrointestinal stromal tumors HSDN C3829611 Nausea frequency C0012644 Animal disease models HSDN C0013404 Respiratory difficulty C0014170 Endometrial neoplasms HSDN C1384666 Decreased hearing C0043167 Pertussis HSDN C0003079 Pupillary inequality C0342257 Complications of diabetes mellitus HSDN C0037771 Paraparesis spastic C1963178 Myelitis adverse event HSDN C1279888 Proteinuria of undiagnosed cause C1963083 Cholecystitis adverse event HSDN C4085548 Usual severity dizziness C0038356 Stomach neoplasms HSDN C4084802 Usual severity diarrhea C0920350 Autoimmune thyroiditis HSDN C0000737 Abdomen pain C0344315 Depressed mood HSDN C0013421 Dystonia C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C2315100 Pediatric failure to thrive C1850053 Pelizaeus-merzbacher-like disease, autosomal recessive, 2 MalaCards|HPO C0151686 Growth retardation C4015253 Mitochondrial complex iii deficiency, nuclear type 9 MalaCards C2242996 Tingling C0023465 Acute monocytic leukemia HSDN C4085317 Diarrhea frequency C0398689 Hyper-igm immunodeficiency syndrome, type 1 HPO C0413252 Hypothermia due to exposure C0497327 Dementia HSDN C0085631 Abnormal excitement C0034494 Rabies (disorder) DiseaseOntology|MalaCards C0037383 Sneeze C0027051 Myocardial infarction HSDN C0557874 Global developmental delay C3151000 Hemorrhagic destruction of the brain, subependymal calcification, and cataracts MalaCards|HPO C4085211 Pain distress question C0015459 Face injury HSDN C1963180 Neck pain adverse event C0002949 Aneurysm, dissecting HSDN C0034155 Thrombotic thrombocytopenic purpura C0023055 Laryngeal neoplasm HSDN C3887873 Hearing loss C0022904 Lacrimal apparatus diseases HSDN C0557874 Global developmental delay C3554316 Epileptic encephalopathy, early infantile, 15 MalaCards C0030486 Extremity paralysis, lower C0023798 Lipoma HSDN C0151740 Intracranial hypertension C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|HPO|MalaCards C0013421 Dystonia C0022660 Kidney failure, acute HSDN C2315100 Pediatric failure to thrive C0432443 Deletion of long arm of chromosome 18 MalaCards C0242936 Center pain C0003047 Animal disease HSDN C4085548 Usual severity dizziness C0006663 Calcinosis HSDN C2315100 Pediatric failure to thrive C0268250 Gaucher disease, type 2 (disorder) MalaCards|HPO C2242996 Tingling C0023518 Leukocytosis HSDN C0151786 Weakness muscle C0038941 Incisional infection HSDN C0033774 Skin pruritus C0027947 Neutropenia HSDN C0013404 Respiratory difficulty C0079027 Blood loss, surgical HSDN C0015672 Decreased energy C0036341 Schizophrenia HSDN C0037317 Sleep disturbance C3151140 Pontocerebellar hypoplasia, type 2d HPO|UMLS C1963093 Dizziness adverse event C1457883 Aggressive reaction HSDN C0019079 Bloody sputum C1336153 Stage iia adenosquamous cell carcinoma of lung UMLS C2984058 Have pain C0041311 Tuberculosis, female genital HSDN C0018681 Headache, cephalalgia C0157743 Vibratory urticaria MalaCards C4084767 Bothered by vomiting C3536715 Aa amyloidosis MalaCards C4084767 Bothered by vomiting C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0019209 Large liver C3492932 Lactic acidosis, congenital infantile, due to lad deficiency MalaCards C0151889 Reflexes tendon increased C1847725 Spinocerebellar ataxia 15 MalaCards C4084727 Cough frequency C1550639 Specimen type - fistula HSDN C0004604 Pain back C0022665 Kidney neoplasm HSDN C0009792 Consciousness disorder C3163620 Hypotension adverse event HSDN C4085317 Diarrhea frequency C0001546 Adjustment disorders HSDN C0042571 Vertigo subjective C0033893 Tension headache HSDN C0522224 Palsied C0040715 Chromosomal translocation HSDN C0003862 Pain joint C0221390 Non-bacterial thrombotic endocarditis HSDN C0234132 Pyramidal sign C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C2911645 Weight loss adverse event C1835664 Tylosis with esophageal cancer MalaCards C0518090 Frequency of pain question C0553980 Endomyocardial fibrosis HSDN C1963281 Vomiting adverse event C0024115 Lung diseases HSDN C0013604 Edematous C0020621 Hypokalemia HSDN C0018681 Headache, cephalalgia C1336037 Inverted papilloma of sphenoid sinus UMLS C0018784 Deafness sensorineural C0026760 Multiple epiphyseal dysplasia OrphaNet|MalaCards C1963170 Hypothermia adverse event C0002878 Anemia, hemolytic HSDN C0008031 Pain chest C0022665 Kidney neoplasm HSDN C0042963 Symptoms vomiting C0024198 Lyme disease HSDN C2237041 Shox gene with short stature C1844862 Abruzzo erickson syndrome OrphaNet|HPO|MalaCards C0349588 Stature short C0085920 Brachial neuralgia MalaCards C4084724 Usual severity constipation C0030297 Pancreatic neoplasm HSDN C0151786 Weakness muscle C1865290 Hyperinsulinemic hypoglycemia, familial, 3 MalaCards C1000483 Genus anemia C1860168 Achondroplasia, so-called, and severe combined immunodeficiency MalaCards C2984058 Have pain C1175175 Severe acute respiratory syndrome HSDN C0009806 Constipate C0027765 Nervous system disorder HSDN C0042571 Vertigo subjective C0023895 Liver diseases HSDN C0015469 Facial paralysis C1850386 Giant axonal neuropathy 1 MalaCards|HPO C0016382 Cutaneous vascular engorgement C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0015672 Decreased energy C0878683 Pituitary dwarfism type 3 MalaCards C0035229 Respiratory function impaired C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0151908 Dry skin C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards|UMLS C0028738 Nystagmus C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C2315100 Pediatric failure to thrive C1857276 Trichohepatoenteric syndrome MalaCards|HPO C0030193 Sense of pain C0037417 Identification, social HSDN C0012833 Dizzy C1510412 Pseudoaneurysm HSDN C0020305 Fetal edema C0018802 Congestive heart failure HSDN C0030193 Sense of pain C0855051 Extraskeletal osteosarcoma, nonmetastatic UMLS C0042798 Vision dim C1423873 Cone-rod dystrophy 9 MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome MalaCards|HPO C4085211 Pain distress question C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0151786 Weakness muscle C1837218 Cleft palate, isolated HSDN C0234979 Dysdiadochokinesia C1843884 Spinocerebellar ataxia 18 UMLS C0860603 Anxiety symptom C0041408 Turner syndrome OrphaNet|MalaCards C0851578 Disorder sleep C0040188 Tic disorder HSDN C0011991 Loose stools C0030790 Pelvis infection HSDN C4085210 Usual severity pain C0022595 Keratosis follicularis HSDN C0018681 Headache, cephalalgia C1175175 Severe acute respiratory syndrome DiseaseOntology|MalaCards C0454644 Delayed language development C0268632 Homocarnosinosis MalaCards C2984058 Have pain C0031190 Persistent fetal circulation syndrome HSDN C1549543 Administration method - pain C0042065 Genitourinary neoplasms HSDN C0848203 Male pelvic pain C0002989 Epithelioid hemangioma of skin HSDN C0018681 Headache, cephalalgia C1332302 Anterior foramen magnum meningioma UMLS C0042024 Urine incontinence C3806730 Mental retardation, x-linked 98 MalaCards C0233514 Behavior abnormal C0018523 Hallervorden-spatz syndrome MalaCards|HPO C0024031 Back pain lower back C0085271 Self-injurious behavior HSDN C4085661 Usual severity nausea C0021818 Intervertebral disk displacement HSDN C0027796 Neuralgias C0751932 Internal popliteal neuropathies HSDN C0575081 Abnormal gait C2931534 Cloverleaf skull and bone dysplasias MalaCards C4084775 Usual severity weight loss C1704272 Benign prostatic hyperplasia HSDN C3641755 Have constipation C0023890 Liver cirrhosis HSDN C0015468 Face pain C0025286 Meningioma HSDN C3887873 Hearing loss C0003469 Anxiety disorders HSDN C0004093 Asthenia C0033578 Prostatic neoplasms HSDN C0042571 Vertigo subjective C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C0086565 Liver function abnormal C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0454644 Delayed language development C0221060 Mobius syndrome MalaCards C4084774 Have weight loss C0018188 Granuloma HSDN C0008031 Pain chest C0014170 Endometrial neoplasms HSDN C0034150 Skin purpura C1306759 Eosinophilic disorder HSDN C0015672 Decreased energy C0035436 Rheumatic fever OrphaNet|HSDN|MalaCards C0002170 Alopecia disorders C1274795 Urban schosser spohn syndrome OrphaNet|MalaCards C0018784 Deafness sensorineural C2911643 Encounter due to family history of osteoporosis HSDN C0011991 Loose stools C0037356 Smallpox virus HSDN C4084766 Vomiting C1857855 Spastic paraplegia 29, autosomal dominant MalaCards C2132198 Abnormal blistering of the skin C0281479 Primary systemic amyloidosis MalaCards C0002962 Angina C0700208 Acquired scoliosis HSDN C0039591 Testicle pain C2711897 Pain in testicle as late effect of injury to testicle UMLS C0030193 Sense of pain C0152110 Meralgia paresthetica UMLS C2919142 Short stature adverse event C0017920 Glycogen storage disease type i OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C1963137 Hydrocephalus adverse event HSDN C0034150 Skin purpura C0475801 Leukemia, prolymphocytic, b-cell HSDN C0034933 Abnormal reflexes C0006436 Burning electric HSDN C0015672 Decreased energy C0279083 Cgl, meningeal UMLS C0000737 Abdomen pain C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C4084723 Constipation C4049644 Depression HSDN C0151786 Weakness muscle C0040409 Tongue diseases HSDN C2936821 Spinal cerebrospinal fluid leak C0007760 Cerebellar diseases HSDN C0002622 Amnesias C0752347 Lewy body disease HSDN C0009806 Constipate C0042138 Uterine neoplasms HSDN C1963252 Tremor adverse event C0032787 Postoperative complications HSDN C0151786 Weakness muscle C2028283 History of premature birth HSDN C4084766 Vomiting C0041327 Tuberculosis, pulmonary HSDN C4084769 Vomiting frequency C0020701 Somatization disorder HSDN C0232466 Feeding difficulty C2675527 Myopathy, congenital, compton-north MalaCards C0042798 Vision dim C0079504 Hermanski-pudlak syndrome MalaCards C3829611 Nausea frequency C0037397 Behavior social HSDN C0009806 Constipate C0262655 Recurrent urinary tract infection HSDN C1549543 Administration method - pain C0041309 Tuberculosis, cutaneous HSDN C4084774 Have weight loss C2609414 Acute kidney injury HSDN C0033774 Skin pruritus C0571833 Niacin allergy UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C1879737 Aromatherapy and essential oils HSDN C0018772 Deafness C0001824 Agranulocytosis HSDN C1527344 Dysphonia C0026896 Myasthenia gravis HSDN C3829611 Nausea frequency C0007222 Cardiovascular diseases HSDN C0028738 Nystagmus C0751038 Cockayne syndrome, type ii HPO C0043352 Absent salivary secretion C0158667 Aplasia of lacrimal and salivary glands MalaCards|HPO C4085222 Nausea C0022650 Kidney calculi HSDN C0000731 Abdomen distention C0281508 Desmoplastic small round cell tumor OrphaNet|HPO|MalaCards C2984058 Have pain C2116082 Finding of thyroid nodule by palpation HSDN C0427068 Legs weakness C1334698 Meningothelial cell neoplasm MalaCards C0009806 Constipate C1707436 Colon signet ring cell adenocarcinoma UMLS C0040822 D tremors C0010324 Crigler najjar syndrome, type 1 MalaCards|HPO C0036572 Convulsion C0015328 Behavior, exploratory HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1720887 Female urogenital diseases HSDN C3641755 Have constipation C1970431 Pitt-hopkins syndrome MalaCards|HPO C0232462 Appetite decrease C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0034065 Pulmonary embolism HSDN C0036659 Sensation disorder C0033860 Psoriasis HSDN C0018784 Deafness sensorineural C2674004 Von hippel-lindau syndrome, modifiers of HPO C0036572 Convulsion C0220730 Fryns syndrome OrphaNet|UMLS|HPO|MalaCards C2032396 Pelvic pain on the right C0221752 Rbc urine HSDN C0026838 Spasticity muscle C0027643 Neoplasm recurrence, local HSDN C1557397 Adverse event associated with pain C0376154 Skin callus HSDN C0917816 Deficiency mental C1855080 Microcephaly-cardiomyopathy syndrome MalaCards C0349588 Stature short C2718068 Beta-galactosidase deficiency OrphaNet|MalaCards C0035021 Fever, famine C0852654 21-hydroxylase deficiency MalaCards C0027066 Myoclonic jerking C1864923 Northern epilepsy syndrome MalaCards C1963091 Diarrhea adverse event C0149678 Epstein-barr virus infections HSDN C3274924 Have been coughing C0003838 Arterial occlusive diseases HSDN C0022346 Yellow skin C0279606 Childhood hepatocellular carcinoma UMLS C0000737 Abdomen pain C0041466 Typhoid fever OrphaNet|HSDN|MalaCards C0010200 Cough symptom C0011981 Diaphragmatic eventration HSDN C0013428 Painful urination C1306759 Eosinophilic disorder HSDN C0004134 Dyssynergia C0268242 Niemann-pick disease, type a MalaCards C3274924 Have been coughing C1290398 Cerebral arterial aneurysm HSDN C1963063 Anorexia adverse event C0023788 Whipple disease OrphaNet|MalaCards C0018520 Breath odor C0027651 Tumor HSDN C2362324 Pediatric obesity C0020459 Hyperinsulinism HSDN C0001707 Aerophagia C0004048 Breathing HSDN C2911645 Weight loss adverse event C0038436 Post-traumatic stress disorder HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0032851 Disease poultry HSDN C0035229 Respiratory function impaired C2674173 Achondroplasia, severe, with developmental delay and acanthosis nigricans HPO C4084727 Cough frequency C0004364 Autoimmune diseases HSDN C2029884 Hearing loss by exam C0032453 Polychondritis, relapsing HSDN C4085548 Usual severity dizziness C0546884 Hypovolemia HSDN C0032617 High urine output C1857395 De toni-debre-fanconi syndrome HPO C3641755 Have constipation C0238015 Autonomic dysreflexia HSDN C0013395 Indigestion C1708349 Hereditary diffuse gastric cancer UMLS C4084802 Usual severity diarrhea C0848377 Trauma to the abdomen HSDN C1971624 Appetite absent C0024899 Mastocytosis MalaCards C1963091 Diarrhea adverse event C0041466 Typhoid fever DiseaseOntology|HSDN|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0039373 Tay-sachs disease HSDN C2984058 Have pain C0021832 Intestinal diseases, parasitic HSDN C0521634 Female genital itching C0236100 Disorders female reproductive UMLS C0151740 Intracranial hypertension C2931196 Craniofacial dysostosis type 1 MalaCards C0042024 Urine incontinence C1706377 Memory device component HSDN C0009806 Constipate C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease OrphaNet|HPO C0231528 Muscle pain generalized C0221056 Adult type dermatomyositis OrphaNet|MalaCards C0042798 Vision dim C1842914 Adult-onset vitelliform macular dystrophy OrphaNet|HPO|MalaCards C0040822 D tremors C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0151686 Growth retardation C0796016 Microphthalmia, syndromic 1 MalaCards|HPO C1557397 Adverse event associated with pain C0027126 Myotonic dystrophy HSDN C4084775 Usual severity weight loss C0023290 Leishmaniasis, visceral DiseaseOntology C3814530 Skin vesicle C0263398 Erythema elevatum diutinum OrphaNet|MalaCards C1963063 Anorexia adverse event C0018671 Head and neck neoplasms HSDN C0002962 Angina C0037926 Compression of spinal cord HSDN C3146279 Coma C0011616 Contact dermatitis HSDN C0033377 Caudal displacement C1860464 Congenital ptosis and posterior fusion of lumbosacral vertebrae OrphaNet|MalaCards C0035229 Respiratory function impaired C3146222 Idiopathic aortitis MalaCards C0040264 Ear ringing sound C0040053 Thrombosis HSDN C2919142 Short stature adverse event C1860789 Leukemia, megakaryoblastic, of down syndrome HPO C0151826 Pain chest substernal C0023092 Lassa fever MalaCards C0009421 Comatose C0024115 Lung diseases HSDN C0042928 Paralysis vocal cord C0010068 Coronary heart disease HSDN C0221166 Paraparesis C4023792 Paraplegia/paraparesis UMLS C0349588 Stature short C0271585 Isolated trh deficiency MalaCards C0036572 Convulsion C0422847 Postural seizure UMLS C0264272 Nose discharge, purulent C0745283 Infectious process UMLS C2911645 Weight loss adverse event C0031154 Peritonitis HSDN C1999266 Depression adverse event C3494506 Pseudohypoparathyroidism, type ia HPO C0349588 Stature short C1832408 Hunter-mcalpine craniosynostosis syndrome MalaCards C0020673 Hypothermia (central) (local) C0243026 Sepsis HSDN C0020580 Decreased sensation C0860603 Anxiety symptoms HSDN C4084802 Usual severity diarrhea C0005758 Bulla HSDN C0030486 Extremity paralysis, lower C1546602 Specimen source codes - diverticulum HSDN C0242936 Center pain C0033785 Pseudarthrosis HSDN C0011570 Monopolar depression C1856491 Gaucher disease, type iiia HPO C0023014 Developmental disorder language C0265240 Goldenhar syndrome HSDN C0011991 Loose stools C0006271 Bronchiolitis HSDN C3463815 Feel fatigue C0035042 Psychology and religion HSDN C4085210 Usual severity pain C0009953 Convulsive therapy HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0003504 Aortic valve insufficiency HSDN C0030193 Sense of pain C0751895 Vasospasm, intracranial HSDN C4084768 Usual severity vomiting C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO C4084784 Diarrhea C0334489 Pancreatoblastoma OrphaNet|MalaCards C4084784 Diarrhea C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0013604 Edematous C0027666 Neoplasms, radiation-induced HSDN C0007166 Cardiac output decreased C0007873 Uterine cervical neoplasm HSDN C0013404 Respiratory difficulty C0038325 Stevens-johnson syndrome HSDN|HPO C0015970 Fever unknown origin C0037999 Splenic neoplasms HSDN C0030193 Sense of pain C1336079 Squamous cell breast carcinoma UMLS C0003862 Pain joint C0398689 Hyper-igm immunodeficiency syndrome, type 1 HSDN C2911647 Weight gain adverse event C0001175 Acquired immunodeficiency syndrome HSDN C1384666 Decreased hearing C0011854 Diabetes mellitus, insulin-dependent HSDN C4084767 Bothered by vomiting C1963088 Cystitis adverse event HSDN C0004134 Dyssynergia C0013336 Dwarfism HSDN C4084723 Constipation C0018523 Hallervorden-spatz syndrome OrphaNet|MalaCards C4084784 Diarrhea C0004782 Basal ganglia diseases HSDN C0522224 Palsied C0036980 Shock, cardiogenic HSDN C0024032 Birth weight subnormal C1856891 Faciocardiomelic dysplasia, lethal MalaCards C0042798 Vision dim C2936245 Flow, optic HSDN C0031911 Pigment deposition C1306247 Melanotic neurilemmoma MalaCards C0015402 Hemorrhage eye C0032797 Postpartum hemorrhage HSDN C0018772 Deafness C0009404 Colorectal neoplasms HSDN C3463815 Feel fatigue C1510415 Osteosclerotic myeloma MalaCards C0010520 Skin cyanosis C2939465 Deficiency of glucose-6-phosphate dehydrogenase HSDN C0042940 Disorder of voice C0038454 Cerebrovascular accident HSDN C0003469 Anxiety disorder C0751434 Classical phenylketonuria MalaCards|HPO C0030552 Paralysis partial C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards C0004134 Dyssynergia C0000744 Abetalipoproteinemia OrphaNet|UMLS|HPO|MalaCards C3274924 Have been coughing C0021933 Intussusception HSDN C2984058 Have pain C0019270 Hernia HSDN C0349588 Stature short C1835794 Kallmann syndrome 2 with bimanual synkinesia HPO C0015672 Decreased energy C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C1963065 Apnea adverse event C2931398 Arachnodactyly, abnormal ossification and mental retardation MalaCards C0022408 Disorder joint C2931420 Brachydactylous dwarfism mseleni type OrphaNet C0518090 Frequency of pain question C0043253 Trauma blunt HSDN C4084802 Usual severity diarrhea C0030500 Animal parasitic disease HSDN C0000737 Abdomen pain C0425045 Sudden infant death HSDN C0030193 Sense of pain C1336311 Paranasal sinus cancer stage ii UMLS C1963249 Tinnitus adverse event C0010674 Cystic fibrosis HSDN C0013604 Edematous C0035436 Rheumatic fever HSDN C1963281 Vomiting adverse event C0014335 Enteritis HSDN C4084724 Usual severity constipation C0018790 Cardiac arrest HSDN C0018524 Hallucinate C0013922 Embolism HSDN C2984058 Have pain C0021845 Intestinal perforation HSDN C2203646 Jaundice C1962963 Osteoporosis adverse event HSDN C0002965 Crescendo angina C0038436 Post-traumatic stress disorder HSDN C0024031 Back pain lower back C0026976 Myelitis, transverse HSDN C0036572 Convulsion C0007282 Carotid stenosis HSDN C0036572 Convulsion C0517555 Venous thrombosis after immobility HSDN C0003862 Pain joint C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0013604 Edematous C0021845 Intestinal perforation HSDN C1384666 Decreased hearing C1844862 Abruzzo erickson syndrome MalaCards|HPO C1963071 Back pain adverse event C0041188 Pyomyositis, tropical HSDN C2364111 Gustatory anesthesia C0037824 Intelligibilities, speech HSDN C4085549 Dizziness C0026269 Mitral valve stenosis HSDN C0242936 Center pain C0030804 Pemphigoid, benign mucous membrane HSDN C0518090 Frequency of pain question C0015806 Femur neck fracture HSDN C0000737 Abdomen pain C0314657 Genetic predisposition HSDN C0033774 Skin pruritus C0003615 Appendicitis HSDN C0424755 Fever symptoms C0028432 Nose diseases HSDN C0036572 Convulsion C1848552 Methylmalonic aciduria and homocystinuria, cbld type OrphaNet|UMLS|HPO|MalaCards C1963063 Anorexia adverse event C0024620 Primary malignant neoplasm of liver MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0010701 Phyllodes tumor HSDN C0518090 Frequency of pain question C0362046 Prediabetes syndrome HSDN C0018991 Paralysis one side of body C4041080 Neurocognitive disorders HSDN C0040822 D tremors C2239176 Liver carcinoma HSDN C0234146 Absent reflex C0265201 De sanctis-cacchione syndrome MalaCards|HPO C0030193 Sense of pain C3662826 Lumbar discogenic pain UMLS C4084802 Usual severity diarrhea C0206692 Carcinoma, lobular HSDN C1963249 Tinnitus adverse event C0812393 Cancer patients and suicide and depression HSDN C0003862 Pain joint C0458219 Complex regional pain syndromes HSDN C0085650 Purpura fulminans C0026764 Multiple myeloma HSDN C0036572 Convulsion C3151036 Chromosome 1p32-p31 deletion syndrome HPO|UMLS C0018681 Headache, cephalalgia C0270861 Migraines retinal UMLS C0042798 Vision dim C0037744 Perceptual spatial orientation HSDN C2029884 Hearing loss by exam C0025286 Meningioma HSDN C4020887 Photodysphoria C2931411 Flotch syndrome OrphaNet|MalaCards C0013362 Dysarthrias C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C0518090 Frequency of pain question C0001396 Stokes-adams syndrome HSDN C0242936 Center pain C0038166 Staphylococcal skin infections HSDN C0040485 Wryneck C0376527 Neoplasm, skull base HSDN C4084727 Cough frequency C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C1279888 Proteinuria of undiagnosed cause C0035066 Renal artery obstruction HSDN C4084788 Have dizziness C0014175 Endometriosis HSDN C0037036 Increased salivation C3502054 Dentoleukoencephalopathy MalaCards C0013421 Dystonia C0026848 Myopathy HSDN|UMLS C0424755 Fever symptoms C1963067 Atrial fibrillation adverse event HSDN C0018784 Deafness sensorineural C0026764 Multiple myeloma HSDN C4085210 Usual severity pain C0036330 Schistosomiasis mansoni HSDN C0424755 Fever symptoms C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C1963071 Back pain adverse event C0018099 Gout HSDN C4085317 Diarrhea frequency C0032302 Mycoplasma pneumonia HSDN C0004134 Dyssynergia C0268138 Xeroderma pigmentosum, complementation group d HPO|UMLS C0151786 Weakness muscle C0038436 Post-traumatic stress disorder HSDN C3641756 Have diarrhea C0026771 Trauma multiple HSDN C0020580 Decreased sensation C0393534 Paraneoplastic cerebellar degeneration HSDN C0013404 Respiratory difficulty C2242987 Benign mastocytoma MalaCards C1963063 Anorexia adverse event C0262584 Carcinoma, small cell HSDN C4084802 Usual severity diarrhea C0007124 Noninfiltrating intraductal carcinoma HSDN C0007758 Cerebellar ataxia C0149678 Epstein-barr virus infections HSDN C0043352 Absent salivary secretion C1862939 Amyotrophic lateral sclerosis 1 MalaCards C4084723 Constipation C0020676 Hypothyroidism HSDN C0015469 Facial paralysis C2609414 Acute kidney injury HSDN C0349588 Stature short C0268414 Hyperphosphatasemia with bone disease OrphaNet|HPO|MalaCards C0002622 Amnesias C0037369 Smoking HSDN C0012833 Dizzy C0039980 Chest injury HSDN C2911645 Weight loss adverse event C0428478 Serum triglycerides raised HSDN C0018681 Headache, cephalalgia C0259779 Fibrous dysplasia HSDN C0018926 Emesis bloody C2718087 Vitamin k deficiency bleeding HSDN C3665346 Loss sight C3164344 Adult onset autosomal dominant leukodystrophy HPO C0003910 Articulation disorder C0040435 Tooth diseases HSDN C0007758 Cerebellar ataxia C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C3887873 Hearing loss C0009241 Cognition disorders HSDN C1963093 Dizziness adverse event C0853697 Neutrophil count decreased HSDN C0522224 Palsied C0006736 Body stone HSDN C1549543 Administration method - pain C0242973 Ventricular dysfunction HSDN C1963170 Hypothermia adverse event C0024312 Lymphopenia HSDN C0010038 Corneal opacity disorder C0268228 Neuraminidase 1 deficiency OrphaNet C3829611 Nausea frequency C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2220167 Skin lesion on both sides of lower lip C0037284 Skin lesion UMLS C1384666 Decreased hearing C0027831 Neurofibromatosis 1 OrphaNet C4084766 Vomiting C0036982 Shock, hemorrhagic HSDN C0022408 Disorder joint C0018995 Hemochromatosis OrphaNet C0026821 Cramp C0003803 Arnold chiari malformation HSDN C4085642 Level of joint stiffness C0795864 Smith-magenis syndrome MalaCards|HPO C1963093 Dizziness adverse event C2713543 Biofeedback eeg HSDN C0042024 Urine incontinence C0019655 Histoplasmosis HSDN C1963281 Vomiting adverse event C0023176 Lead poisoning MalaCards C4084769 Vomiting frequency C0019061 Hemolytic-uremic syndrome HSDN C0851578 Disorder sleep C0040128 Thyroid diseases HSDN C0020455 Hypergammaglobulinemia C0001197 Acrodermatitis HSDN C0013362 Dysarthrias C2930923 N-acetylneuraminic acid storage disease MalaCards C0086437 Joint hypermobility C0751156 Fraxa syndrome OrphaNet|HPO|MalaCards C1069915 Vertigo C0029888 Otitis media purulent HSDN C2911647 Weight gain adverse event C0037275 Skin diseases, vesiculobullous HSDN C2096293 Ent surgical result ear vertigo C0019557 Hip fx HSDN C0016199 Pain flank C0040053 Thrombosis HSDN C0426579 Anorexia symptom C0235974 Pancreatic carcinoma MalaCards C0010200 Cough symptom C0011127 Pressure ulcer HSDN C0917816 Deficiency mental C2675897 1q21.1 contiguous gene deletion OrphaNet|HPO|MalaCards C0012833 Dizzy C0010276 Craniopharyngioma MalaCards|HPO C1963091 Diarrhea adverse event C0026683 Mucocele HSDN C0393588 Dystonias paroxysmal C1855565 Pyruvate dehydrogenase e2 deficiency MalaCards|HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C1546949 Event consequence - death HSDN C0152459 Striae C0344479 Spinal cord myelodysplasia HSDN C0007166 Cardiac output decreased C0007137 Squamous cell carcinoma HSDN C4084726 Distress cough C0085786 Hamman-rich syndrome MalaCards|HSDN C0002962 Angina C0027667 Cancer origin unknown HSDN C1963063 Anorexia adverse event C0162637 Strongylida infections HSDN C0520909 Ponv C0004623 Bacterial infections HSDN C3827868 Tachycardia by ecg finding C0024591 Malignant hyperpyrexia due to anesthesia HPO C0042024 Urine incontinence C0497580 Condylomata acuminata in men HSDN C0035232 Diaphragmatic paralysis C0013264 Muscular dystrophy, duchenne HSDN C0017672 Pain tongue C0011570 Mental depression HSDN C0015970 Fever unknown origin C0024630 Malingering HSDN C1384666 Decreased hearing C0265246 Townes syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0043528 Zoonoses HSDN C0022346 Yellow skin C1258104 Diffuse scleroderma HSDN C0018772 Deafness C0003125 Anorexia nervosa HSDN C0021359 Infertility C0268301 Reifenstein syndrome OrphaNet|HPO C0019079 Bloody sputum C0025222 Melena HSDN C0009806 Constipate C0518449 Control of hip fracture risk HSDN C0454644 Delayed language development C4014435 Mental retardation, autosomal dominant 26 MalaCards C0013404 Respiratory difficulty C0206061 Pneumonia, interstitial UMLS C0011991 Loose stools C0850614 Diarrhea, psychogenic UMLS C0017565 Gingiva hemorrhage C0265321 Wyburn-mason syndrome MalaCards C4084773 Bothered by weight gain C0027726 Nephrotic syndrome HSDN C0019079 Bloody sputum C0032285 Pneumonia UMLS C4085210 Usual severity pain C0001080 Achondroplasia HSDN C0043094 Weight gain C0013575 Ectodermal dysplasia HSDN C0162835 Hypopigmentation C1868679 Griscelli syndrome, type 2 MalaCards|HPO C4085549 Dizziness C0023676 Life style HSDN C2911647 Weight gain adverse event C0023441 Leukemia, experimental HSDN C4020887 Photodysphoria C1832976 Cone-rod dystrophy 5 MalaCards|HPO C0029163 Hemorrhage mouth C0031085 Periodontal abscess HSDN C4085211 Pain distress question C0221018 Hereditary sideroblastic anemia HSDN C4084725 Usual severity cough C0748164 Pulmonary nodule multiple HSDN C1557397 Adverse event associated with pain C0027658 Neoplasms, germ cell and embryonal HSDN C0027796 Neuralgias C0262584 Carcinoma, small cell HSDN C2919142 Short stature adverse event C1857568 Cortical blindness, retardation, and postaxial polydactyly OrphaNet|MalaCards C0086439 Activity decreased C0524812 Intracranial hypotension HSDN C0237326 Defecation pain C3493776 Hypothyroidism, congenital, nongoitrous, 1 MalaCards C2911645 Weight loss adverse event C0026896 Myasthenia gravis HSDN C0018808 Murmur C1556682 Adverse event associated with infection HSDN C0241210 Speaking delay C1835088 Maxillofacial dysostosis MalaCards C0413252 Hypothermia due to exposure C0037397 Behavior social HSDN C0040034 Thrombocytopenia C0393639 Hashimoto's encephalitis MalaCards C0917816 Deficiency mental C0796182 Acromelic frontonasal dysplasia MalaCards C0557874 Global developmental delay C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C4084726 Distress cough C0031903 Pigeon breeder's lung MalaCards C0000737 Abdomen pain C0037397 Behavior social HSDN C0426579 Anorexia symptom C1858592 Carney triad MalaCards C0040034 Thrombocytopenia C3151441 Dyskeratosis congenita, autosomal recessive 2 MalaCards|HPO C0018780 Frequencies hearing high loss C0027439 Nasopharyngeal neoplasms HSDN C2203646 Jaundice C0546323 Inferior vena cava membranous obstruction MalaCards C0002962 Angina C0003851 Arteriosclerosis obliterans HSDN C0030193 Sense of pain C0242658 Homosexuality male HSDN C0030200 Intractable pain C0023903 Liver neoplasms HSDN C0000737 Abdomen pain C1333081 Colloid carcinoma of the pancreas UMLS C1963281 Vomiting adverse event C0333355 Inflammatory disease of mucous membrane HSDN C0013604 Edematous C0014849 Esophageal and gastric varices HSDN C1279888 Proteinuria of undiagnosed cause C0007787 Transient ischemic attack HSDN C0002965 Crescendo angina C0021818 Intervertebral disk displacement HSDN C0027796 Neuralgias C0040053 Thrombosis HSDN C0917816 Deficiency mental C0016037 Fibrodysplasia ossificans progressiva MalaCards|HPO C3887873 Hearing loss C0006434 Burn injury HSDN C0424755 Fever symptoms C0014059 Encephalomyelitis, acute disseminated HSDN C0013604 Edematous C0027813 Neuritis HSDN C1384666 Decreased hearing C3541306 Plasmodium measurement HSDN C3887638 Failure to thrive in infant C2930798 Alexanders leukodystrophy MalaCards C0018681 Headache, cephalalgia C0585442 Osteosarcoma of bone HSDN C0034150 Skin purpura C1546654 Specimen source codes - granuloma HSDN C0424755 Fever symptoms C0014013 Empyema, pleural DiseaseOntology|HSDN C1963087 Constipation adverse event C0524851 Neurodegenerative disorders HSDN C0018965 Blood urine C1302282 Chromaffin cell neoplasm MalaCards C0009421 Comatose C0023702 Injury lightning HSDN C0019572 Hairiness C0040765 Transsexualism HSDN C0008031 Pain chest C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome OrphaNet|MalaCards C0018834 Brash C2931557 Chromosome 4 short arm deletion MalaCards C4084776 Weight loss C0007134 Renal cell carcinoma HSDN C4085210 Usual severity pain C0009241 Cognition disorders HSDN C1963252 Tremor adverse event C1848533 Ataxia with vitamin e deficiency HPO C1963252 Tremor adverse event C0042812 Acuity visual HSDN C1963087 Constipation adverse event C0004114 Astrocytoma HSDN C1963065 Apnea adverse event C0031212 Personality disorders HSDN C4060792 Itching (e.g., eyes, facial, nasal, oral) C0812341 Latex allergy response UMLS C3665347 Vision impaired C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0018784 Deafness sensorineural C0026848 Myopathy HSDN C0497247 Blood pressure elevation C1449844 Pseudohypoaldosteronism, type ii OrphaNet|MalaCards C0178417 Anhedonia C0015457 Expression facial HSDN C4085211 Pain distress question C0013240 Alveolar osteitis HSDN C1549543 Administration method - pain C0085136 Central nervous system neoplasms HSDN C0022346 Yellow skin C0036415 Sclerema neonatorum nos HSDN C4082202 Sleep quality question C0085209 Bovine spongiform encephalitis MalaCards C0234518 Speech slurred C0406587 Wrinkly skin syndrome MalaCards C0454644 Delayed language development C2673873 Bardet-biedl syndrome 13 HPO C4084802 Usual severity diarrhea C0002357 Altruism HSDN C0206146 Myocardial stunning C0009375 Colonic neoplasms HSDN C0003962 Ascites C0023903 Liver neoplasms MalaCards C0000727 Abdomen acute C2103077 Disorder of jejunum and ileum UMLS C0036572 Convulsion C0007001 Carbohydrate metabolism, inborn errors HSDN C1963065 Apnea adverse event C3812141 Linc00914 gene HSDN C4085210 Usual severity pain C1334928 Necrotic changes (finding) HSDN C0042963 Symptoms vomiting C1963084 Colitis adverse event HSDN C4085317 Diarrhea frequency C0039103 Synovitis HSDN C0042928 Paralysis vocal cord C0014850 Esophageal atresia HSDN C0018784 Deafness sensorineural C0265293 Frontometaphyseal dysplasia OrphaNet|HPO|MalaCards C4085211 Pain distress question C0014236 Endophthalmitis HSDN C0015469 Facial paralysis C0021051 Immunologic deficiency syndromes HSDN C2029884 Hearing loss by exam C0036202 Sarcoidosis HSDN C0242936 Center pain C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0232466 Feeding difficulty C1849348 Richieri costa pereira syndrome MalaCards|HPO C1557397 Adverse event associated with pain C1956089 Osteophyte HSDN C0241210 Speaking delay C0268543 Hyperammonemia, type iii MalaCards C4085211 Pain distress question C0018023 Nodular goiter HSDN C1290771 Edema of oral vestibule C0035204 Respiration disorders UMLS C0013428 Painful urination C0950124 Papillomavirus infections HSDN C4084767 Bothered by vomiting C0009240 Cognition HSDN C0030975 Disorders perception C0012691 Dislocations HSDN C0000737 Abdomen pain C1332248 Ampulla of vater mucinous adenocarcinoma UMLS C0085631 Abnormal excitement C0272414 Displaced spleen HSDN C3829611 Nausea frequency C0242658 Homosexuality male HSDN C0030193 Sense of pain C0039496 Temporomandibular joint dysfunction syndrome UMLS C1557397 Adverse event associated with pain C0152025 Polyneuropathy HSDN C0026205 Pupillary constriction C1303009 Microcoria, congenital MalaCards C2984058 Have pain C0015618 Families therapy HSDN C0349588 Stature short C1860119 Acrofacial dysostosis syndrome of rodriguez MalaCards C0040822 D tremors C0022660 Kidney failure, acute HSDN C0030232 Color loss C0021295 Infant, premature, diseases HSDN C4085862 Bothered by nausea C0026266 Mitral valve insufficiency HSDN C0271215 Blindness legal C1864689 Microphthalmia, syndromic 6 (disorder) MalaCards|HPO C0575081 Abnormal gait C2749936 Spastic paraplegia 18, autosomal recessive (disorder) MalaCards|HPO C1963071 Back pain adverse event C3887678 Cpnet MalaCards C2220048 Bilateral knee joint pain C1866717 Spondyloepiphyseal dysplasia tarda, autosomal dominant MalaCards|UMLS C0020673 Hypothermia (central) (local) C0025007 Measles HSDN C0037763 Spasm C0264412 Extrinsic asthma - no status UMLS C3178766 Nociceptive pain C0011385 Dental occlusion, traumatic HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C0340493 Paroxysmal familial ventricular fibrillation MalaCards C4085210 Usual severity pain C0080178 Spina bifida HSDN C1549543 Administration method - pain C1963119 Stomach ulcer adverse event HSDN C3463815 Feel fatigue C0242658 Homosexuality male HSDN C0030193 Sense of pain C0042341 Varicocele HSDN C0019079 Bloody sputum C0009995 Cor triatriatum HSDN C4084802 Usual severity diarrhea C0020179 Huntington disease HSDN C0033377 Caudal displacement C1862261 Bpes, type ii HPO C2984058 Have pain C0025048 Meconium aspiration syndrome HSDN C2911645 Weight loss adverse event C0013182 Drug allergy HSDN C0518090 Frequency of pain question C0002514 Amino acid metabolism, inborn errors HSDN C0013404 Respiratory difficulty C0854889 Advanced malignant mesothelioma of pleura UMLS C0040485 Wryneck C0343525 Lemierre syndrome HSDN C0242936 Center pain C1306710 Facial asymmetry HSDN C3887638 Failure to thrive in infant C0795851 14 trisomy mosaicism syndrome OrphaNet|MalaCards C0040034 Thrombocytopenia C0220704 Shprintzen syndrome MalaCards|HPO C4084774 Have weight loss C0034929 Reflex HSDN C0018784 Deafness sensorineural C1862839 Anterior segment mesenchymal dysgenesis MalaCards C0013404 Respiratory difficulty C0018944 Hematoma HSDN C1963063 Anorexia adverse event C0004936 Mental disorders HSDN C0031911 Pigment deposition C1368295 Malignant basal cell tumor MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3814778 Hemolytic index HSDN C0026821 Cramp C0152181 Hypoglossal nerve disease or syndrome HSDN C0033774 Skin pruritus C0020620 Hypohidrosis HSDN C0027796 Neuralgias C0018800 Cardiomegaly HSDN C0032285 Pneum C3553512 Immunodeficiency, common variable, 8, with autoimmunity MalaCards C0020672 Body temperature decreased C0030922 Peptic ulcer hemorrhage HSDN C0349489 Fetal hypoxia C0021400 Influenza HSDN C0003467 Angst C0221033 Trisomy x syndrome MalaCards C0018834 Brash C0236969 Substance-related disorders HSDN C0030193 Sense of pain C0521665 Chronic mixed headache syndrome UMLS C0018775 Hearing loss bilateral C0751908 Vestibular neuronitis HSDN C0036572 Convulsion C0156677 Eclampsia; pregnancy UMLS C4084784 Diarrhea C0020039 Hostility HSDN C0020580 Decreased sensation C0001175 Acquired immunodeficiency syndrome HSDN C0018772 Deafness C0007873 Uterine cervical neoplasm HSDN C0033774 Skin pruritus C3489795 Hyper-ige recurrent infection syndrome, autosomal dominant OrphaNet|HPO C0851578 Disorder sleep C0006434 Burn injury HSDN C3539895 Pelvic pain occurs with bowel movement C0042029 Urinary tract infection HSDN C0015468 Face pain C0006663 Calcinosis HSDN C0034155 Thrombotic thrombocytopenic purpura C0019054 Hemolysis (disorder) HSDN C0151889 Reflexes tendon increased C1969796 Ataxia, spastic, 2, autosomal recessive (disorder) MalaCards|HPO C0242936 Center pain C0812470 Abortion, incomplete HSDN C0042755 Virilisation C0033944 Psychosexual development HSDN C4085661 Usual severity nausea C0032227 Pleural effusion disorder HSDN C0000737 Abdomen pain C0341480 Pancreas, cyst, congenital MalaCards C2203646 Jaundice C0023364 Leptospirosis DiseaseOntology|MalaCards C1963184 Nystagmus adverse event C1846496 Gaze palsy, familial horizontal, with progressive scoliosis OrphaNet|HPO C0017565 Gingiva hemorrhage C1866983 Scleroderma, familial progressive MalaCards C0428977 Pulse rate decrease C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C4084802 Usual severity diarrhea C0162538 Immunoglobulin a deficiency (disorder) HSDN C2032396 Pelvic pain on the right C1546847 Entity name part type - family HSDN C4085211 Pain distress question C0030469 Paranasal sinus diseases HSDN C0042963 Symptoms vomiting C3887523 Very long chain acyl-coa dehydrogenase deficiency UMLS C1263846 Attention deficit disorder with hyperactivity C0038505 Sturge-weber syndrome OrphaNet|HPO C0242936 Center pain C0019156 Hepatic veno-occlusive disease HSDN C0030552 Paralysis partial C0029882 Otitis media HSDN C2096293 Ent surgical result ear vertigo C1704972 Genomic orientation HSDN C2032396 Pelvic pain on the right C0019693 Hiv infections HSDN C0042928 Paralysis vocal cord C0038395 Streptococcal infections HSDN C0034155 Thrombotic thrombocytopenic purpura C0017178 Gastrointestinal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033927 Psychopathology HSDN C2024893 Cardiovascular surgery result: fatigue C0003794 Arm injury HSDN C1263846 Attention deficit disorder with hyperactivity C1263846 Attention deficit hyperactivity disorder MalaCards C1000483 Genus anemia C0406355 Acrokeratosis paraneoplastica of bazex OrphaNet|MalaCards C0853986 Lymphocytes decreased C1969799 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation MalaCards C1384666 Decreased hearing C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C0851578 Disorder sleep C0024117 Chronic obstructive airway disease HSDN C0023012 Delay language C0010314 Cri-du-chat syndrome MalaCards C0030193 Sense of pain C0018839 Heat exhaustion HSDN C0242936 Center pain C0020655 Hypothalamic diseases HSDN C0018777 Deafness, conductive C1847800 Waardenburg syndrome type 1 MalaCards C0004134 Dyssynergia C0751267 Encephalopathy, subacute necrotizing, infantile OrphaNet|MalaCards C4084768 Usual severity vomiting C0017416 Genital neoplasms, female HSDN C0036572 Convulsion C0079772 T-cell lymphoma HSDN C0042024 Urine incontinence C0043251 Wounds and injuries HSDN C0028961 Urine output decreased C0002351 Altitude sickness HSDN C0011991 Loose stools C0033626 Protein deficiency HSDN C0000737 Abdomen pain C1962976 Ventricular fibrillation adverse event HSDN C0013404 Respiratory difficulty C0014544 Epilepsy HSDN C0030193 Sense of pain C0855052 Extraosseous osteosarcoma UMLS C1384666 Decreased hearing C1306577 Dies patient HSDN C0033774 Skin pruritus C3178970 Entrapment, pudendal nerve MalaCards C0233794 Memory impaired C0027831 Neurofibromatosis 1 OrphaNet C2024893 Cardiovascular surgery result: fatigue C0027743 Nerve compression syndrome HSDN C4084775 Usual severity weight loss C0003615 Appendicitis HSDN C0034150 Skin purpura C0027947 Neutropenia HSDN C4085661 Usual severity nausea C1956418 Torsion abnormality HSDN C4085211 Pain distress question C0002514 Amino acid metabolism, inborn errors HSDN C2984058 Have pain C0015347 Extinction HSDN C0012569 Double vision C0011581 Depressive disorder HSDN C0848203 Male pelvic pain C0034065 Pulmonary embolism HSDN C0860277 Sour stomach C0151713 Hyperchlorhydria UMLS C0010200 Cough symptom C2931785 Juvenile dermatomyositis MalaCards C3539896 Pelvic pain occurs with urination C0314657 Genetic predisposition HSDN C0025287 Meningitis-like C1963137 Hydrocephalus adverse event HSDN C4085862 Bothered by nausea C0011609 Drug eruptions HSDN C0030552 Paralysis partial C1963137 Hydrocephalus adverse event HSDN C3463815 Feel fatigue C1552262 Nurse practitioner - family HSDN C0010200 Cough symptom C0342443 Adrenal cushing's syndrome HSDN C1527344 Dysphonia C2116082 Finding of thyroid nodule by palpation HSDN C3641755 Have constipation C0206247 Amyloid neuropathies MalaCards C4084774 Have weight loss C0017128 Fistula gastric HSDN C0012833 Dizzy C2609414 Acute kidney injury HSDN C0030193 Sense of pain C2911243 Encounter due to family history of colonic polyps HSDN C0562483 Cough persistent C2919453 Persistent cough after viral respiratory infection UMLS C1963071 Back pain adverse event C0021933 Intussusception HSDN C4085661 Usual severity nausea C0018671 Head and neck neoplasms HSDN C0002622 Amnesias C0033906 Psychological theories HSDN C0040264 Ear ringing sound C0752160 Hemangioma, cavernous, central nervous system HSDN C3898969 Have been vomiting C0037199 Sinusitis HSDN C3463815 Feel fatigue C0005967 Bone neoplasms HSDN C0036572 Convulsion C0020502 Hyperparathyroidism HSDN C1527344 Dysphonia C0030354 Papilloma HSDN C0040264 Ear ringing sound C0002895 Anemia, sickle cell HSDN C0349681 Spontaneous nystagmus C0028738 Nystagmus UMLS C0155552 Hearing loss mixed C0014065 Congenital cerebral hernia HSDN C0036572 Convulsion C0346303 Thyrotroph adenoma MalaCards C0013428 Painful urination C0038325 Stevens-johnson syndrome HPO C4085211 Pain distress question C0008441 Chondroblastoma HSDN C0018772 Deafness C1275079 Acps iii MalaCards C4085862 Bothered by nausea C0220847 C hepatitis virus HSDN C0018775 Hearing loss bilateral C1956346 Coronary artery disease HSDN C0036659 Sensation disorder C1704771 Association class HSDN C0005745 Blepharoptosis C3714043 Trisomy xq28 OrphaNet|HPO C1384666 Decreased hearing C3888317 Sialidosis, type 2 OrphaNet C0030193 Sense of pain C0029396 Heterotopic ossification HSDN C2029884 Hearing loss by exam C0016542 Foreign body HSDN C4084767 Bothered by vomiting C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0008031 Pain chest C0009186 Coccidioidomycosis MalaCards|HSDN C0022346 Yellow skin C3273033 Well differentiated hepatocellular carcinoma UMLS C0040485 Wryneck C0022758 Kap HSDN C0015230 Exanthem C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C0007398 Catatonic C0004935 Animal ethology HSDN C0547030 Sensory perceptual alteration: visual C3648167 Late effects of nontraumatic subarachnoid hemorrhage vision disturbances UMLS C3887638 Failure to thrive in infant C0020725 Type ii mucolipidosis OrphaNet|HPO|MalaCards C0036572 Convulsion C3150705 Foxg1 syndrome HPO|UMLS C4085211 Pain distress question C0265334 Pachyonychia congenita HSDN C4085210 Usual severity pain C0812470 Abortion, incomplete HSDN C0036572 Convulsion C4014343 Mental retardation, autosomal recessive 42 MalaCards C2203646 Jaundice C0016542 Foreign body HSDN C0027497 Queasy C0009187 Coccidiosis HSDN C4084726 Distress cough C0042133 Uterine fibroids HSDN C3887638 Failure to thrive in infant C0266015 Congenital digestive system anomalies HSDN C1963184 Nystagmus adverse event C1859305 Cerebellar ataxia and hypogonadotropic hypogonadism OrphaNet|HPO C2911645 Weight loss adverse event C0030807 Pemphigus, nos HSDN C0003113 Anomia C0011269 Dementia, vascular HSDN C0851578 Disorder sleep C0032963 Pregnancy complications, cardiovascular HSDN C0020458 Hyperhydrosis C3146222 Idiopathic aortitis MalaCards C0557874 Global developmental delay C3898580 Loeys-dietz syndrome type 2 MalaCards C4084776 Weight loss C0003047 Animal disease HSDN C0278152 Hemifacial spasms C0752165 Angioma, venous, central nervous system HSDN C1963154 Renal failure adverse event C0037054 Sickle cell trait MalaCards C0002965 Crescendo angina C0004275 Attitude health HSDN C0026838 Spasticity muscle C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO|UMLS C0004134 Dyssynergia C0085078 Lysosomal storage diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0162820 Dermatitis, allergic contact HSDN C0020672 Body temperature decreased C0242231 Coronary stenosis HSDN C0030193 Sense of pain C0410005 Nodular fasciitis UMLS C0018772 Deafness C2675463 Chromosome 15q26-qter deletion syndrome MalaCards C0007758 Cerebellar ataxia C0029134 Optic neuritis HSDN C0518090 Frequency of pain question C0009447 Common variable immunodeficiency HSDN C0030486 Extremity paralysis, lower C0013289 Duodenal diseases HSDN C4085317 Diarrhea frequency C0276932 Schistosoma; intercalatum DiseaseOntology C1961131 Cough adverse event C0017563 Gingival diseases HSDN C3539023 Pelvic pain increasing in frequency C0751792 Trauma, nervous system HSDN C0007859 Pain neck C0428953 Ecg infarction myocardial HSDN C0042963 Symptoms vomiting C0023374 Lesch-nyhan syndrome MalaCards|HPO|UMLS C1963093 Dizziness adverse event C0022660 Kidney failure, acute HSDN C0030552 Paralysis partial C0001125 Acidosis, lactic HSDN C0015468 Face pain C0282333 Relaxation therapies HSDN C0234518 Speech slurred C1852467 Creutzfeldt-jakob disease, sporadic MalaCards C0019521 Hiccoughs C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN C4042891 Sleep wake disorders C0027092 Myopia HSDN C0010200 Cough symptom C0007282 Carotid stenosis HSDN C0015676 Mental fatigue C0011570 Mental depression HSDN C0018784 Deafness sensorineural C0752138 Intracranial arterial diseases HSDN C0002962 Angina C1704421 Skin pigmentation disorder HSDN C1557397 Adverse event associated with pain C0011428 Dentigerous cyst HSDN C0028738 Nystagmus C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0007095 Carcinoid tumor HSDN C4084725 Usual severity cough C0162820 Dermatitis, allergic contact HSDN C0030193 Sense of pain C0236733 Amphetamine-related disorders HSDN C3641756 Have diarrhea C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C0036572 Convulsion C0856761 Budd-chiari syndrome HSDN C1112616 Loss of proprioception C1836916 Posterior column ataxia with retinitis pigmentosa UMLS C4085549 Dizziness C0017160 Gastroenteritis HSDN C0034155 Thrombotic thrombocytopenic purpura C0008626 Congenital chromosomal disease HSDN C0424755 Fever symptoms C0024236 Lymphedema HSDN C1279888 Proteinuria of undiagnosed cause C0220989 Acquired partial lipodystrophy MalaCards|HPO C2237041 Shox gene with short stature C1832615 Hyperparathyroidism, neonatal severe OrphaNet|HPO C2315100 Pediatric failure to thrive C0432291 Mandibuloacral dysostosis MalaCards C0018524 Hallucinate C0021831 Intestinal diseases HSDN C1963090 Dehydration adverse event C1855116 Methylmalonic aciduria, mut(-) type HPO C1279888 Proteinuria of undiagnosed cause C0997768 Glaucoma HSDN C1962972 Proteinuria adverse event C0011303 Demyelinating diseases HSDN C2984057 Have nausea C0004030 Aspergillosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0010054 Coronary arteriosclerosis HSDN C0030193 Sense of pain C0242994 Hantavirus infections HSDN C1069915 Vertigo C0151467 Addisonian crisis MalaCards C1549543 Administration method - pain C1258215 Ileus HSDN C0277959 Hair coarseness C0029294 Orofaciodigital syndromes MalaCards C0010200 Cough symptom C0264455 Bronchitis due to fumes and vapors UMLS C2315100 Pediatric failure to thrive C0221036 Acrodermatitis enteropathica OrphaNet|HPO C0023014 Developmental disorder language C0015671 Father HSDN C3898969 Have been vomiting C1550639 Specimen type - fistula HSDN C0006370 Bulimia C0031090 Periodontal diseases HSDN C4085210 Usual severity pain C0025500 Mesothelioma HSDN C3898969 Have been vomiting C1304456 Congo hemorrhagic fever MalaCards C0039870 Leanness C0038356 Stomach neoplasms HSDN C0010520 Skin cyanosis C0344315 Depressed mood HSDN C0028738 Nystagmus C3810326 Spinocerebellar ataxia, autosomal recessive 15 MalaCards C0019825 Voice hoarseness C0013449 Ear neoplasms HSDN C0027796 Neuralgias C0016169 Pathologic fistula HSDN C1963184 Nystagmus adverse event C0271889 Diencephalic syndrome of infancy OrphaNet|MalaCards C0151686 Growth retardation C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C0557874 Global developmental delay C1859301 Cerebellar hypoplasia with endosteal sclerosis MalaCards C4084767 Bothered by vomiting C0334489 Pancreatoblastoma OrphaNet|MalaCards C4084788 Have dizziness C2984572 Malaria pathway HSDN C0085636 Light sensitivity C1864966 Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features UMLS C0015672 Decreased energy C1691228 Cystic kidney diseases HSDN C1279888 Proteinuria of undiagnosed cause C0033054 Prenatal exposure delayed effects HSDN C4084726 Distress cough C0018944 Hematoma HSDN C2126063 Bilateral exophthalmos C3541319 Short stature, optic nerve atrophy, and pelger-huet anomaly MalaCards|UMLS C0026838 Spasticity muscle C0041948 Uremia HSDN C3641756 Have diarrhea C0001815 Primary myelofibrosis HSDN C0002962 Angina C0013295 Duodenal ulcer HSDN C2919142 Short stature adverse event C0265451 Chromosome 13q deletion syndrome MalaCards C0035078 Failure kidney C0031069 Familial mediterranean fever HPO C0015970 Fever unknown origin C0019163 Hepatitis b HSDN C0009676 Confusion state C1510428 Cerebral abscess HSDN C0013421 Dystonia C0027873 Neuromyelitis optica HSDN C0042963 Symptoms vomiting C0520799 Acute radiation syndrome HSDN C4085661 Usual severity nausea C1509147 Histiocytoma HSDN C0011991 Loose stools C0025149 Medulloblastoma HSDN C2032395 Pelvic pain on the left C1299262 Sarcoma - category (morphologic abnormality) HSDN C1579931 Depressed - symptom C0751072 Frontotemporal lobar degeneration MalaCards C1549543 Administration method - pain C0009766 Allergic conjunctivitis HSDN C0851578 Disorder sleep C0037019 Shy-drager syndrome HSDN C3898969 Have been vomiting C0018799 Heart diseases HSDN C0232943 Metromenorrhagia C0079504 Hermanski-pudlak syndrome OrphaNet|MalaCards C4084774 Have weight loss C0030920 Peptic ulcer HSDN C0427055 Face weakness C0854906 Benign schwannoma OrphaNet|MalaCards C0518090 Frequency of pain question C0003646 Aptitude HSDN C0557874 Global developmental delay C1291329 Transaldolase deficiency MalaCards|HPO C0042571 Vertigo subjective C0008370 Cholestasis HSDN C1579931 Depressed - symptom C2675897 1q21.1 contiguous gene deletion MalaCards C1963170 Hypothermia adverse event C0019699 Hiv seropositivity HSDN C0151889 Reflexes tendon increased C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C4084769 Vomiting frequency C0009319 Colitis HSDN C0037771 Paraparesis spastic C0006309 Brucellosis HSDN C1557397 Adverse event associated with pain C0001126 Renal tubular acidosis HSDN C0850149 Cough dry C1175175 Severe acute respiratory syndrome DiseaseOntology|MalaCards C0020438 Hypercalciuria C0030521 Parathyroid neoplasms MalaCards|HSDN C0851578 Disorder sleep C0206172 Diabetic foot HSDN C0015672 Decreased energy C0003047 Animal disease HSDN C0221166 Paraparesis C0347766 Skull fracture depressed HSDN C3463815 Feel fatigue C0031118 Peripheral nervous system neoplasms HSDN C0008031 Pain chest C0009171 Cocaine abuse UMLS C4084802 Usual severity diarrhea C1527336 Sjogren's syndrome HSDN C1260880 Nasal drip C1335340 Accessory sinus mucoepidermoid carcinoma UMLS C0026838 Spasticity muscle C1850599 Leigh syndrome due to mitochondrial complex iv deficiency HPO C4084724 Usual severity constipation C0026857 Musculoskeletal diseases HSDN C0242936 Center pain C0041408 Turner syndrome HSDN C0042024 Urine incontinence C0001580 Adolescent behavior HSDN C0006370 Bulimia C0030305 Pancreatitis HSDN C1963281 Vomiting adverse event C3149848 Variegate porphyria, homozygous variant HPO C3665386 Abnormal vision C3495438 Macular degeneration, age-related, 2 MalaCards C0010200 Cough symptom C0031154 Peritonitis HSDN C0027796 Neuralgias C0021390 Inflammatory bowel diseases HSDN C4085549 Dizziness C2936631 Complaint, subjective health HSDN C0040822 D tremors C0017636 Glioblastoma HSDN C0026821 Cramp C0012979 Canine disease HSDN C0003862 Pain joint C0917990 Acro-osteolysis HSDN C0042025 Urinary incontinence stress C0041976 Urethritis HSDN C0026826 High muscle tone C0399523 Class i malocclusion HSDN C4084766 Vomiting C1522133 High cholesterol level HSDN C0030193 Sense of pain C1332579 Bone leiomyosarcoma UMLS C1971624 Appetite absent C0001430 Adenoma HSDN C0026826 High muscle tone C0795830 Chromosome 9p deletion syndrome OrphaNet|MalaCards C2032395 Pelvic pain on the left C0206654 Leiomyomatosis HSDN C0020538 Hbp C4014361 Abdominal obesity-metabolic syndrome 3 MalaCards C0231218 Malaise generalized C1541448 Recurrent grade i angiocentric immunoproliferative lesions UMLS C0003962 Ascites C0268151 Classical galactosemia MalaCards C2237041 Shox gene with short stature C1858593 Limb-girdle muscular dystrophy, type 2e MalaCards C1963170 Hypothermia adverse event C0020542 Pulmonary hypertension HSDN C0022346 Yellow skin C1142389 Subicteric UMLS C0030193 Sense of pain C0018889 Helminthiasis HSDN C0000727 Abdomen acute C0006736 Body stone HSDN C0520904 Postoperative nausea C1285297 Gastrointestinal complication of procedure UMLS C3815497 Cough C0233629 Thinking and speaking disturbances HSDN C0575081 Abnormal gait C1847640 Kufor-rakeb syndrome MalaCards C0152459 Striae C0877015 Pelvic organ prolapse HSDN C0242936 Center pain C0030186 Paget disease extramammary HSDN C3146279 Coma C0751955 Brain infarction HSDN C0267373 Bleeding intestine C1332262 Anal canal squamous cell carcinoma MalaCards C3463815 Feel fatigue C0007766 Intracranial aneurysm HSDN C4085661 Usual severity nausea C0042373 Vascular diseases HSDN C0030193 Sense of pain C0006114 Cerebral edema HSDN C0028738 Nystagmus C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C0860603 Anxiety symptom C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C0011991 Loose stools C0037072 Diseases sigmoid HSDN C4084776 Weight loss C0042076 Urologic neoplasms HSDN C4084802 Usual severity diarrhea C0242634 Diseases primates HSDN C0033774 Skin pruritus C0812393 Cancer patients and suicide and depression HSDN C0152169 Colic renal C0340629 Aortic aneurysm without mention of rupture nos HSDN C2128959 Middle-night awakening with dry mouth C0393761 Fitful sleep UMLS C1963077 Bone pain adverse event C2749485 Nblst1 HPO C0005745 Blepharoptosis C0032339 Rothmund-thomson syndrome MalaCards C1557397 Adverse event associated with pain C0024266 Lymphocytic choriomeningitis HSDN C4084802 Usual severity diarrhea C0030790 Pelvis infection HSDN C0015672 Decreased energy C0013481 Ebstein anomaly OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0008350 Cholelithiasis HSDN C2984058 Have pain C0040441 Broken teeth HSDN C0013604 Edematous C0702221 Tactual discrimination HSDN C3887638 Failure to thrive in infant C1846044 Adrenomyodystrophy OrphaNet|MalaCards C1963091 Diarrhea adverse event C0002170 Alopecia HSDN C1000483 Genus anemia C0678213 Complete hydatidiform mole MalaCards C0036572 Convulsion C2677682 Rett syndrome, zappella variant HPO C0042963 Symptoms vomiting C0037315 Sleep apnea syndromes HSDN C2984057 Have nausea C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse HSDN C0700072 Encounter due to stillbirth C1844696 Otopalatodigital syndrome, type ii HPO C2984058 Have pain C0006281 Congenital bronchogenic cyst HSDN C0750937 Appendicular ataxia C0398746 Gluthathione synthetase deficiency MalaCards C2128730 Proximal left leg soft tissue swelling C0037580 Soft tissue swelling UMLS C0518090 Frequency of pain question C0026766 Multiple organ failure HSDN C0007859 Pain neck C2102996 Disorders of peripheral nerve, neuromuscular junction and muscle UMLS C0030554 Abnormal sensation C0023890 Liver cirrhosis HSDN C0033774 Skin pruritus C0038395 Streptococcal infections HSDN C1963091 Diarrhea adverse event C1306503 Congenital exomphalos HSDN C4085211 Pain distress question C0041341 Tuberous sclerosis HSDN C4084774 Have weight loss C0014121 Bacterial endocarditis HSDN C0917816 Deficiency mental C1855675 Arima syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C1009209 Tinea HSDN C0026826 High muscle tone C0751664 Canavan disease, neonatal MalaCards C3665492 Pigmentations C0079504 Hermanski-pudlak syndrome MalaCards C3887638 Failure to thrive in infant C3809971 Asparagine synthetase deficiency MalaCards C1963091 Diarrhea adverse event C3814778 Hemolytic index HSDN C0018965 Blood urine C0220987 Hereditary orotic aciduria MalaCards C0221263 Cafe au lait spot C0004779 Basal cell nevus syndrome HSDN C1838869 Proximal neurogenic muscle weakness C3714932 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 MalaCards C0018681 Headache, cephalalgia C1868599 Parietal foramina 1 MalaCards|HPO C0009806 Constipate C0003123 Anorexia UMLS C0349588 Stature short C0086651 Mucopolysaccharidosis, mps-iv-a OrphaNet|MalaCards C4084775 Usual severity weight loss C0039494 Temporomandibular joint disorders HSDN C1549543 Administration method - pain C0560694 Bottles per feed HSDN C0034124 Pupillary disorder C0029124 Optic atrophy HSDN C3887873 Hearing loss C3494473 Myringoscleroses HSDN C4084774 Have weight loss C0020545 Hypertension, renovascular HSDN C0028738 Nystagmus C0040560 Toxoplasmosis, congenital MalaCards C4085211 Pain distress question C0013010 Cerebral lateralization HSDN C2984057 Have nausea C0393735 Headache disorders HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1258104 Diffuse scleroderma HSDN C4085210 Usual severity pain C0022572 Keratoacanthoma HSDN C0009460 Communication impairment C0525042 Feeding and eating disorders of childhood HSDN C3463815 Feel fatigue C0003864 Arthritis HSDN C1963071 Back pain adverse event C0007781 Intracranial embolism and thrombosis HSDN C3815497 Cough C3463824 Myelodysplastic syndrome HSDN C0410919 Foetal bradycardia C2118398 Fetal bradycardia during labor UMLS C0242936 Center pain C0028432 Nose diseases HSDN C0011991 Loose stools C0007787 Transient ischemic attack HSDN C0011168 Disorder deglutition C0038505 Sturge-weber syndrome HPO C0002962 Angina C0001815 Primary myelofibrosis HSDN C0007758 Cerebellar ataxia C0037286 Skin neoplasms HSDN C0018681 Headache, cephalalgia C1336040 Sphenoorbital meningioma UMLS C0497406 Over weight C2984299 Asthma pathway HSDN C0033377 Caudal displacement C0796279 Carnevale syndrome MalaCards|HPO C0242936 Center pain C0015395 Burn eye HSDN C0018808 Murmur C0016658 Fracture bone HSDN C4085317 Diarrhea frequency C0039520 Tenosynovitis HSDN C0042571 Vertigo subjective C0015414 Eye neoplasms HSDN C0018777 Deafness, conductive C0033586 Failure, prosthesis HSDN C2919142 Short stature adverse event C1859312 Camfak syndrome OrphaNet|HPO C4084784 Diarrhea C0027439 Nasopharyngeal neoplasms HSDN C0700590 Diaphoresis excessive C0342686 Aromatic amino acid decarboxylase deficiency MalaCards C0878773 Bladder hyperactive C0751932 Internal popliteal neuropathies HSDN C1549543 Administration method - pain C0013806 Electroplexy shock therapy HSDN C4084784 Diarrhea C1270972 Mild cognitive disorder HSDN C0232466 Feeding difficulty C1837371 Sudden infant death with dysgenesis of the testes syndrome MalaCards C1145670 Failure respiratory C0024507 Majewski syndrome MalaCards C2911645 Weight loss adverse event C0006012 Borderline personality disorder HSDN C0004604 Pain back C1837218 Cleft palate, isolated HSDN C1145670 Failure respiratory C1849438 Renal dysplasia-limb defects syndrome MalaCards C0162835 Hypopigmentation C0268496 Kramer syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0022423 Judgement HSDN C4085211 Pain distress question C0270857 Epilepsy, reflex HSDN C0221232 Welts C0413245 Sodium benzoate-induced angio-edema-urticaria UMLS C3812171 Bradycardia by ecg finding C1837371 Sudden infant death with dysgenesis of the testes syndrome MalaCards|HPO C0848203 Male pelvic pain C0019066 Nontraumatic hemoperitoneum HSDN C0025287 Meningitis-like C0270629 Epidural abscess HSDN C2911645 Weight loss adverse event C0024692 Mandible fracture HSDN C4085222 Nausea C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C4084725 Usual severity cough C0015663 Fasting HSDN C0454644 Delayed language development C1849158 Insulin-like growth factor i, resistance to, due to increased binding protein HPO C0018784 Deafness sensorineural C0080179 Vertebra fracture HSDN C0011991 Loose stools C0019163 Hepatitis b UMLS C4085210 Usual severity pain C0041601 Ulna fracture HSDN C0009806 Constipate C0039006 Swine--diseases HSDN C0043094 Weight gain C0011389 Dental plaque HSDN C1963167 Memory impairment adverse event C0004943 Behcet syndrome MalaCards|HPO C0037384 Snore C0012979 Canine disease HSDN C0151686 Growth retardation C3280543 Mental retardation, autosomal recessive 24 MalaCards C1549543 Administration method - pain C0006060 Boutonneuse fever HSDN C2919142 Short stature adverse event C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C0021359 Infertility C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C0013395 Indigestion C0005586 Bipolar disorder HSDN C0042928 Paralysis vocal cord C0037286 Skin neoplasms HSDN C0013404 Respiratory difficulty C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0557874 Global developmental delay C2931736 Ehlers-danlos syndrome with progeroid facies and mild mental retardation OrphaNet|MalaCards C0026821 Cramp C0019061 Hemolytic-uremic syndrome HSDN C3898969 Have been vomiting C0268595 Glutaric aciduria, type 1 OrphaNet|HPO C4084784 Diarrhea C0032087 Plant poisoning HSDN C4084784 Diarrhea C0030636 Pasteurella infection HSDN C0000737 Abdomen pain C1706377 Memory device component HSDN C0036572 Convulsion C0035613 Rift valley fever MalaCards C0027497 Queasy C0017152 Gastritis HSDN C4084723 Constipation C0237873 Physiological sexual disorders HSDN C2911647 Weight gain adverse event C3536741 Discordant ventriculoarterial connection HSDN C4084784 Diarrhea C0011311 Dengue fever MalaCards|HSDN C0030554 Abnormal sensation C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C0019079 Bloody sputum C0854994 Metastatic epidermoid cell carcinoma of lung UMLS C4085210 Usual severity pain C0018805 Heart injuries HSDN C0575081 Abnormal gait C1836472 Nemaline myopathy 6 HPO C0206160 Retic count elevated C1306589 Congenital dyserythropoietic anemia, type ii HPO C1962972 Proteinuria adverse event C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4084775 Usual severity weight loss C0997768 Glaucoma HSDN C0518090 Frequency of pain question C0040435 Tooth diseases HSDN C0020673 Hypothermia (central) (local) C0020676 Hypothyroidism HSDN C0018772 Deafness C0015745 Ingestive behavior HSDN C0042798 Vision dim C0085209 Bovine spongiform encephalitis MalaCards C4084766 Vomiting C0006145 Breast diseases HSDN C0010520 Skin cyanosis C0030297 Pancreatic neoplasm HSDN C0042963 Symptoms vomiting C0020445 Hypercholesterolemia, familial HSDN C0020672 Body temperature decreased C0460137 Push down or depress HSDN C3641756 Have diarrhea C0020619 Hypogonadism HSDN C0004093 Asthenia C0270952 Muscular dystrophy, oculopharyngeal HSDN C0022346 Yellow skin C0278698 Childhood hepatoma, group iii UMLS C4085210 Usual severity pain C0024793 Marek disease HSDN C4085862 Bothered by nausea C1837218 Cleft palate, isolated HSDN C0030193 Sense of pain C0233315 Premature birth of newborn HSDN C0034150 Skin purpura C0010068 Coronary heart disease HSDN C0012833 Dizzy C0016045 Fibroma HSDN C2984057 Have nausea C1963084 Colitis adverse event HSDN C0013390 Cramps menstrual C0000786 Spontaneous abortion HSDN C0020305 Fetal edema C0015934 Fetal growth retardation HSDN C0019209 Large liver C1853736 Congenital disorder of glycosylation, type iib MalaCards|HPO C0040485 Wryneck C1265748 Torsion HSDN C0011991 Loose stools C0221026 X-linked agammaglobulinemia HPO|UMLS C1557397 Adverse event associated with pain C0043255 Stab wound HSDN C4085661 Usual severity nausea C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C0011991 Loose stools C0038395 Streptococcal infections HSDN C0518090 Frequency of pain question C0027540 Necrosis HSDN C0000737 Abdomen pain C1336310 Ovarian yolk sac tumor stage ii UMLS C1961131 Cough adverse event C0038941 Incisional infection HSDN C4084774 Have weight loss C3714514 Infection HSDN C4042891 Sleep wake disorders C0002792 Anaphylaxis HSDN C4084768 Usual severity vomiting C0013299 Duodenogastric reflux HSDN C0042940 Disorder of voice C0003873 Rheumatoid arthritis HSDN C0018681 Headache, cephalalgia C0010414 Infection by cryptococcus neoformans HSDN C0018784 Deafness sensorineural C1838447 Waardenburg syndrome, type 2b (disorder) MalaCards C0003862 Pain joint C0520946 Emotional hypersensitivity HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0016382 Cutaneous vascular engorgement C1836330 Erythrokeratodermia variabilis 3 (disorder) HPO C0040460 Dental pain C0001973 Alcoholic intoxication, chronic HSDN C0036572 Convulsion C0268119 Combined molybdoflavoprotein enzyme deficiency HPO C1963249 Tinnitus adverse event C0036202 Sarcoidosis HSDN C4085549 Dizziness C0014457 Eosinophilia HSDN C0018965 Blood urine C0342749 Glycogen storage disease ic MalaCards|HPO C4084767 Bothered by vomiting C0013182 Drug allergy HSDN C2024893 Cardiovascular surgery result: fatigue C0007453 Cattle disease HSDN C1263846 Attention deficit disorder with hyperactivity C0162671 Melas syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C1959582 Pten hamartoma tumor syndrome MalaCards C0002962 Angina C0242216 Biliary calculi HSDN C2896459 Pain in unspecified foot C0810058 Other connective tissue disease UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0001173 Adult pyloric stenosis HSDN C0024031 Back pain lower back C0022665 Kidney neoplasm HSDN C3887784 Decreased urine output C0024535 Malaria, falciparum HSDN C0750426 Wbc elevated C2931873 Juvenile cranial arteritis MalaCards C1963091 Diarrhea adverse event C0000833 Abscess HSDN C1963071 Back pain adverse event C0041755 Adverse reaction to drug HSDN C4084769 Vomiting frequency C1864498 Renal tubular acidosis, distal, autosomal recessive MalaCards|HPO C0002962 Angina C0013990 Pathological accumulation of air in tissues HSDN C0043094 Weight gain C0034067 Pulmonary emphysema HSDN C0518090 Frequency of pain question C0027149 Myxoma HSDN C0015469 Facial paralysis C0030353 Papilledema HSDN C0020580 Decreased sensation C0022568 Keratitis HSDN C0424755 Fever symptoms C0029191 Orchitis HSDN C1963281 Vomiting adverse event C0269291 Pregnancy heterotopic HSDN C4084726 Distress cough C1761609 Aspiration pneumonitis MalaCards C0035455 Rhinitis C3543826 Ciliary dyskinesia, primary, 19 MalaCards C0522224 Palsied C0206754 Neuroendocrine tumors HSDN C0033774 Skin pruritus C0009450 Disease caused by microorganism HSDN C0036572 Convulsion C0026769 Multiple sclerosis HSDN C4084769 Vomiting frequency C0005779 Blood coagulation disorders HSDN C0013362 Dysarthrias C1859305 Cerebellar ataxia and hypogonadotropic hypogonadism HPO C0039070 Collapse fleeting C0004275 Attitude health HSDN C1963063 Anorexia adverse event C0003615 Appendicitis HSDN C0451941 Itch scrotum C0268919 Scrotum UMLS C3641755 Have constipation C2004491 Cicatrix HSDN C3641756 Have diarrhea C0032066 Plague vaccines HSDN C4084767 Bothered by vomiting C0002726 Amyloidosis HSDN C0149793 Transient monocular blindness C0752143 Intracranial thrombosis HSDN C0086565 Liver function abnormal C3553774 Interstitial nephritis, karyomegalic MalaCards C0018772 Deafness C0030354 Papilloma HSDN C0026821 Cramp C0086768 Pancreatic cholera OrphaNet|MalaCards C1557397 Adverse event associated with pain C0311468 Increased bilirubin level (finding) HSDN C0015672 Decreased energy C0006434 Burn injury HSDN C1961131 Cough adverse event C0036467 Scrofula MalaCards C0002624 Amnesia retrograde C0015347 Extinction HSDN C0018834 Brash C0018802 Congestive heart failure HSDN C0030193 Sense of pain C0041330 Tuberculosis, spinal HSDN C3829611 Nausea frequency C0795623 Hepatitis a vaccine, inactivated HSDN C3887873 Hearing loss C2316212 Cryopyrin-associated periodic syndromes HSDN C0010200 Cough symptom C0016664 Fatigue fracture HSDN C0013604 Edematous C0521169 Fracture compression HSDN C0030552 Paralysis partial C0042131 Uterine diseases HSDN C0003862 Pain joint C0265309 Leri-weill dyschondrosteosis MalaCards C0151786 Weakness muscle C0338437 Neurocysticercosis HSDN C0850758 Pain pelvic C0022410 Joint instability HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C0034933 Abnormal reflexes C0022972 Lambert-eaton myasthenic syndrome HSDN C1963184 Nystagmus adverse event C4014856 Cone-rod dystrophy 20 MalaCards C0027497 Queasy C0235146 Emotionally high HSDN C0020580 Decreased sensation C0026613 Motor skills disorders HSDN C0018772 Deafness C0268386 Amyloid polyneuropathy, swiss type MalaCards C0018772 Deafness C0265449 Pallister-killian syndrome MalaCards C0018681 Headache, cephalalgia C2749561 Nadh-cytochrome b5 reductase deficiency, type i HPO C0013595 Eczematous dermatitis C4053908 Late onset tylosis MalaCards C2919142 Short stature adverse event C1868684 Ear, patella, short stature syndrome MalaCards C1963281 Vomiting adverse event C0017181 Gastrointestinal hemorrhage HSDN C4084802 Usual severity diarrhea C0003855 Arteriovenous fistula HSDN C3641756 Have diarrhea C0020564 Hypertrophy HSDN C0034150 Skin purpura C0037579 Soft tissue neoplasms HSDN C0009421 Comatose C0039590 Testicular neoplasms HSDN C2237041 Shox gene with short stature C0796068 Oculodigitoesophagoduodenal syndrome OrphaNet C0042024 Urine incontinence C0003047 Animal disease HSDN C4084776 Weight loss C0007194 Hypertrophic cardiomyopathy HSDN C4084776 Weight loss C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0234421 Conscious HSDN C0751837 Gait ataxic C0751208 Juvenile huntington disease MalaCards C0278152 Hemifacial spasms C0009088 Cluster headache HSDN C4085549 Dizziness C0264766 Rheumatic mitral stenosis HSDN C0917816 Deficiency mental C2749562 Nadh-cytochrome b5 reductase deficiency, type ii HPO C0853945 Oral mucosa blister C0030804 Pemphigoid, benign mucous membrane OrphaNet|MalaCards C0011991 Loose stools C0008626 Congenital chromosomal disease HSDN C0043094 Weight gain C0702166 Acne HSDN C2911645 Weight loss adverse event C0027540 Necrosis HSDN C0241165 Skin thickening C2931588 Gemss syndrome MalaCards C0004134 Dyssynergia C0017178 Gastrointestinal diseases HSDN C0015672 Decreased energy C1847593 Epiphyseal dysplasia, multiple, 4 MalaCards C1557397 Adverse event associated with pain C0001118 Acid base imbalance HSDN C1279888 Proteinuria of undiagnosed cause C0162871 Aortic aneurysm, abdominal HSDN C0860603 Anxiety symptom C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0424810 Periorbital swelling C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C2315100 Pediatric failure to thrive C0221026 X-linked agammaglobulinemia OrphaNet|HPO C1145670 Failure respiratory C0265374 Warfarin syndrome OrphaNet|MalaCards C1557397 Adverse event associated with pain C0003618 Appetites HSDN C4084774 Have weight loss C0002878 Anemia, hemolytic HSDN C0413252 Hypothermia due to exposure C0038187 Starvation HSDN C0024032 Birth weight subnormal C3495483 Amish brittle hair syndrome MalaCards C0162298 Stiffness joints C0917713 Becker muscular dystrophy OrphaNet C0015672 Decreased energy C0026530 Morales HSDN C3665492 Pigmentations C0751676 Basal cell cancer MalaCards C2030274 Heavy bleeding between periods C0206666 Trophoblastic tumor, placental site OrphaNet|MalaCards C1384666 Decreased hearing C0206307 Canavan disease OrphaNet|HPO|MalaCards C0018524 Hallucinate C0038356 Stomach neoplasms HSDN C1549543 Administration method - pain C0003184 Anthropology HSDN C4084726 Distress cough C0153414 Malignant neoplasm of middle third of esophagus MalaCards C1263846 Attention deficit disorder with hyperactivity C2931817 Chromosome 2q37 deletion syndrome MalaCards|HPO C3539020 Pelvic pain decreasing in frequency C0206687 Carcinoma, endometrioid HSDN C2984058 Have pain C0040820 Trematode infections HSDN C0030193 Sense of pain C0700251 Brachial plexus neuropathies HSDN C0018681 Headache, cephalalgia C0473546 Vibratory angio-edema MalaCards C0018524 Hallucinate C0600091 Identifiers HSDN C2203646 Jaundice C0702094 Agranulocytosis lab result HSDN C4085211 Pain distress question C0553980 Endomyocardial fibrosis HSDN C0030975 Disorders perception C0000768 Congenital abnormality HSDN C4084726 Distress cough C0035956 Rupture spontaneous HSDN C0557874 Global developmental delay C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C0018784 Deafness sensorineural C0264766 Rheumatic mitral stenosis HSDN C0038990 Sweats C1148551 X-linked dyskeratosis congenita MalaCards|HPO C2242996 Tingling C0037313 Sleep HSDN C4084784 Diarrhea C0029883 Otitis media with effusion HSDN C0012833 Dizzy C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards|UMLS C0011168 Disorder deglutition C1834846 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 HPO C0242936 Center pain C0001122 Acidosis HSDN C1963087 Constipation adverse event C0024668 Mammary neoplasms, experimental HSDN C0232461 Increased appetite C1848030 Hypotonia-cystinuria syndrome OrphaNet|HPO|MalaCards C4084788 Have dizziness C0032285 Pneumonia HSDN C0427055 Face weakness C0751335 Scapuloperoneal form of spinal muscular atrophy MalaCards|HPO|UMLS C4084769 Vomiting frequency C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0850758 Pain pelvic C0037072 Diseases sigmoid HSDN C0004604 Pain back C0024299 Lymphoma HSDN C0002965 Crescendo angina C0023798 Lipoma HSDN C0000727 Abdomen acute C0014121 Bacterial endocarditis HSDN C2096293 Ent surgical result ear vertigo C0017612 Glaucoma, open-angle HSDN C3641756 Have diarrhea C0031039 Effusion pericardial HSDN C1963184 Nystagmus adverse event C0339535 Night blindness, congenital stationary MalaCards|HPO C0151686 Growth retardation C0795841 Jacobsen distal 11q deletion syndrome OrphaNet C4084766 Vomiting C0015328 Behavior, exploratory HSDN C0232608 Nose regurgitation C0264388 Aspiration pneumonia due to gastric secretions UMLS C4085211 Pain distress question C0085209 Bovine spongiform encephalitis HSDN C0518090 Frequency of pain question C0747533 Peroneal neuropathy HSDN C2911647 Weight gain adverse event C3495559 Juvenile arthritis HSDN C0040485 Wryneck C0030445 Obstetric paralysis HSDN C1069915 Vertigo C0030422 Extra-adrenal paraganglioma HSDN C2024893 Cardiovascular surgery result: fatigue C2931850 Aase smith syndrome 2 OrphaNet|HPO|MalaCards C0024032 Birth weight subnormal C3887949 Apparent mineralocorticoid excess MalaCards C4085211 Pain distress question C0032319 Pneumopericardium HSDN C0030794 Pelvis pain C0019310 Hernia, obturator HSDN C0344315 Mood depressed C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C2203646 Jaundice C0034359 Cell pus urine HSDN C0042963 Symptoms vomiting C0586323 Alcohol withdrawal seizures UMLS C2881389 Other subjective visual disturbances C0015397 Disorder of eye UMLS C0015672 Decreased energy C0524909 Hepatitis b, chronic MalaCards|HSDN C2237041 Shox gene with short stature C1851801 Eds viib OrphaNet|HPO C0018772 Deafness C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C4084769 Vomiting frequency C0342869 Deficiency of acetyl-coa acyltransferase (disorder) MalaCards C0030554 Abnormal sensation C0024961 Injuries maxillofacial HSDN C0041105 Jaw spasm C0041323 Oral tuberculoses HSDN C0013604 Edematous C0242488 Acute lung injury HSDN C0030552 Paralysis partial C1862941 Amyotrophic lateral sclerosis, sporadic HPO C0521532 Diaphragmatic weakness C1858118 Muscular dystrophy, congenital, 1b MalaCards C0020903 Illusion C0021799 Interprofessional relations HSDN C0012569 Double vision C0014121 Bacterial endocarditis HSDN C0019209 Large liver C4015542 Nephronophthisis 19 MalaCards C0042571 Vertigo subjective C0019163 Hepatitis b HSDN C2077992 Intolerance to wheat gluten C3839943 Wheat intolerance UMLS C0013362 Dysarthrias C4015643 Combined oxidative phosphorylation deficiency 24 MalaCards C0027497 Queasy C0031154 Peritonitis HSDN C0233514 Behavior abnormal C0012236 Digeorge syndrome MalaCards C4085548 Usual severity dizziness C0262584 Carcinoma, small cell HSDN C3887873 Hearing loss C0035243 Respiratory tract infections HSDN C2911645 Weight loss adverse event C0031212 Personality disorders HSDN C4085211 Pain distress question C0005416 Biliary dyskinesia HSDN C0031911 Pigment deposition C0009404 Colorectal neoplasms MalaCards C0027497 Queasy C4050613 Anxiety scale (basc-2) HSDN C0349489 Fetal hypoxia C0042135 Atony uterine HSDN C0018784 Deafness sensorineural C3279948 Deafness, autosomal dominant 64 MalaCards C0262527 Intermittent abdominal pain C0017689 Glucagonoma OrphaNet|MalaCards C0039870 Leanness C0004935 Animal ethology HSDN C0497406 Over weight C0017416 Genital neoplasms, female HSDN C0015672 Decreased energy C0265201 De sanctis-cacchione syndrome MalaCards C0917816 Deficiency mental C3281137 Chromosome 17q12 duplication syndrome MalaCards C0427068 Legs weakness C1858712 Spastic paraplegia 10, autosomal dominant MalaCards|HPO C0857305 Thrombocytopenia purpura C0019163 Hepatitis b HSDN C0018772 Deafness C0220654 Meningeal carcinomatosis HSDN C3463815 Feel fatigue C0001206 Acromegaly OrphaNet|HPO|MalaCards C0015672 Decreased energy C0036974 Shock HSDN C0020672 Body temperature decreased C0038160 Staphylococcal infections HSDN C0024031 Back pain lower back C0042075 Urologic diseases HSDN C0019209 Large liver C2748536 Leukocyte adhesion deficiency, type iii MalaCards C0476273 Distress respiratory C0024534 Malaria, cerebral MalaCards C0151786 Weakness muscle C2706915 Language:-:point in time:^patient:- HSDN C0242936 Center pain C0003708 Arachnitis HSDN C2315100 Pediatric failure to thrive C3150751 Agammaglobulinemia 3, autosomal recessive HPO C1963087 Constipation adverse event C0026850 Muscular dystrophy HSDN C0015300 Ocular proptosis C0795976 Hirsutism-skeletal dysplasia-mental retardation syndrome OrphaNet|MalaCards C1263846 Attention deficit disorder with hyperactivity C1867858 Prader-willi syndrome chromosome region HPO C0009806 Constipate C0042251 Vaginal diseases HSDN C2315100 Pediatric failure to thrive C0033800 Pseudoglioma MalaCards C0151786 Weakness muscle C0008519 Ectopic tissue HSDN C2911645 Weight loss adverse event C0242707 Ventricular dysfunction, right HSDN C0242936 Center pain C0026613 Motor skills disorders HSDN C0042571 Vertigo subjective C0700327 Clinical findings relating to memory HSDN C0038506 Stutter C0031997 Perception, pitch HSDN C0242936 Center pain C2350521 Gustatory perception HSDN C0013528 Echo speech C0017326 Stimulus generalization HSDN C0009421 Comatose C0039726 Disease, thalamic HSDN C0024031 Back pain lower back C0014474 Ependymoma HSDN C1963249 Tinnitus adverse event C3838758 Familial hyperaldosteronism type 3 MalaCards C0043144 Wheeze C0867389 Chronic graft-versus-host disease MalaCards C0242936 Center pain C0004144 Atelectasis HSDN C0004604 Pain back C1546847 Entity name part type - family HSDN C0267373 Bleeding intestine C0019911 Hookworm infections MalaCards C0026821 Cramp C0062527 Hepatitis b vaccine HSDN C1963087 Constipation adverse event C0700208 Acquired scoliosis HSDN C0036572 Convulsion C1332943 Anaplastic childhood oligodendroglioma UMLS C1557397 Adverse event associated with pain C1705810 Generic role HSDN C4084773 Bothered by weight gain C0018099 Gout HSDN C0036572 Convulsion C0016548 Foreign body migration HSDN C0018808 Murmur C0004936 Mental disorders HSDN C2911647 Weight gain adverse event C0009324 Ulcerative colitis HSDN C1279888 Proteinuria of undiagnosed cause C0520679 Sleep apnea, obstructive HSDN C0030486 Extremity paralysis, lower C0018378 Guillain-barre syndrome HSDN C3829611 Nausea frequency C0033578 Prostatic neoplasms HSDN C3665386 Abnormal vision C0027877 Neuronal ceroid-lipofuscinoses OrphaNet|MalaCards C2911647 Weight gain adverse event C0001973 Alcoholic intoxication, chronic HSDN C4084784 Diarrhea C0149931 Migraine disorders HSDN C0878773 Bladder hyperactive C0007222 Cardiovascular diseases HSDN C1557397 Adverse event associated with pain C0005745 Blepharoptosis HSDN C4085211 Pain distress question C0030569 Secondary parkinson disease HSDN C0024031 Back pain lower back C1852521 Spondylocostal dysostosis 4, autosomal dominant MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C3495801 Granulomatosis with polyangiitis HSDN C2127300 Difficulty swallowing hard dry foods C0011168 Deglutition disorders UMLS C0271215 Blindness legal C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0041657 Consciousness loss C0344315 Depressed mood HSDN C3665347 Vision impaired C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C2096293 Ent surgical result ear vertigo C1956346 Coronary artery disease HSDN C4084784 Diarrhea C0472813 X-linked agammaglobulinemia with growth hormone deficiency HPO C0005745 Blepharoptosis C1322286 Thymoma, type c MalaCards C1963063 Anorexia adverse event C0700327 Clinical findings relating to memory HSDN C2237041 Shox gene with short stature C0795959 Gomez lopez hernandez syndrome OrphaNet|MalaCards C0042928 Paralysis vocal cord C1881674 Medical device emits smoke HSDN C0019079 Bloody sputum C1708784 Lung spindle cell carcinoma UMLS C4084726 Distress cough C1000587 Pemphigus HSDN C1961131 Cough adverse event C1550639 Specimen type - fistula HSDN C0277959 Hair coarseness C0021171 Bloch sulzberger syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0020544 Renal hypertension HSDN C4085211 Pain distress question C0036412 Sclera HSDN C4084767 Bothered by vomiting C0023470 Myeloid leukemia HSDN C0018834 Brash C1853099 Cornelia de lange syndrome 3 MalaCards|HPO C1963281 Vomiting adverse event C0040809 Patient refusal of treatment HSDN C0032617 High urine output C0011854 Diabetes mellitus, insulin-dependent MalaCards|UMLS C3641756 Have diarrhea C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0349588 Stature short C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C1963087 Constipation adverse event C0409959 Osteoarthritis, knee HSDN C0023380 Lethargy C0037769 West syndrome HSDN C2077827 Anxiety episodic C0003467 Anxiety UMLS C1069915 Vertigo C1704972 Genomic orientation HSDN C1962972 Proteinuria adverse event C0021400 Influenza HSDN C0026821 Cramp C0024408 Machado-joseph disease MalaCards|HPO|UMLS C1549543 Administration method - pain C0024694 Mandibular neoplasms HSDN C0042024 Urine incontinence C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards C3898969 Have been vomiting C0015814 Femur head necrosis HSDN C0011991 Loose stools C1546558 Specimen source codes - blister HSDN C4084802 Usual severity diarrhea C0870082 Hyperkeratosis HSDN C0011991 Loose stools C0001580 Adolescent behavior HSDN C0033774 Skin pruritus C0017178 Gastrointestinal diseases HSDN C4084724 Usual severity constipation C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C1963170 Hypothermia adverse event C0010308 Congenital hypothyroidism OrphaNet|MalaCards C0018808 Murmur C0038454 Cerebrovascular accident HSDN C4084774 Have weight loss C0025284 Meningeal neoplasms HSDN C0004134 Dyssynergia C0751753 Carbamoyl-phosphate synthase i deficiency disease HSDN|HPO C0031911 Pigment deposition C1306122 Oguchi disease MalaCards C0231528 Muscle pain generalized C0854421 Hanta viral infections MalaCards C4042891 Sleep wake disorders C0022876 Premature obstetric labor HSDN C0015672 Decreased energy C0024299 Lymphoma HSDN|UMLS C0851578 Disorder sleep C0032344 Poisoning aspects HSDN C2024893 Cardiovascular surgery result: fatigue C0039980 Chest injury HSDN C0575081 Abnormal gait C1851920 Dopa-responsive dystonia OrphaNet C0027497 Queasy C0019294 Hernia, inguinal HSDN C0018784 Deafness sensorineural C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0009421 Comatose C0812393 Cancer patients and suicide and depression HSDN C0019079 Bloody sputum C1546654 Specimen source codes - granuloma HSDN C0002622 Amnesias C0018916 Hemangioma HSDN C0013604 Edematous C0085096 Peripheral vascular diseases HSDN C0027497 Queasy C0024305 Lymphoma, non-hodgkin HSDN C0242936 Center pain C0021933 Intussusception HSDN C3898969 Have been vomiting C0019348 Herpes simplex infections HSDN C0042963 Symptoms vomiting C3661523 Congenital intestinal aganglionosis MalaCards C4084776 Weight loss C0004275 Attitude health HSDN C4085317 Diarrhea frequency C0020625 Hyponatremia HSDN C1319541 On examination - right eye proliferative diabetic retinopathy C0154830 Proliferative diabetic retinopathy UMLS C4084776 Weight loss C0020557 Hypertriglyceridemia HSDN C0036572 Convulsion C0085084 Motor neuron disease HSDN C0016199 Pain flank C0002949 Aneurysm, dissecting HSDN C0043094 Weight gain C0020542 Pulmonary hypertension HSDN C0750394 Wbc low C1855115 Methylmalonic aciduria, mut(0) type HPO C4084784 Diarrhea C0149514 Bronchitis acute HSDN C1971624 Appetite absent C0003490 Aortic arch syndrome MalaCards C4085548 Usual severity dizziness C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0011991 Loose stools C0043254 Injuries penetrating HSDN C2187990 Unable to perform sex C0346303 Thyrotroph adenoma OrphaNet|MalaCards C1549543 Administration method - pain C0033941 Psychoses, substance-induced HSDN C0015672 Decreased energy C0039980 Chest injury HSDN C0231835 Respiration rate increased C2677877 Surfactant metabolism dysfunction, pulmonary, 4 MalaCards C1962962 Hyperpigmentation adverse event C1853733 Hemochromatosis, type 4 MalaCards C3665347 Vision impaired C3279875 Cortical malformations, occipital MalaCards C0013604 Edematous C1550639 Specimen type - fistula HSDN C4084726 Distress cough C0037930 Spinal cord neoplasms HSDN C0850758 Pain pelvic C0022865 Obstetric labor complications HSDN C0011991 Loose stools C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C0242936 Center pain C0001249 Actinobacillus infections HSDN C0002962 Angina C0041234 Chagas disease HSDN C4084726 Distress cough C0014461 Granuloma eosinophilic MalaCards C1963087 Constipation adverse event C3281084 Congenital disorder of glycosylation, type ir MalaCards C4084773 Bothered by weight gain C0035435 Rheumatism HSDN C2984057 Have nausea C3150933 Hyperaldosteronism, familial, type iii MalaCards C4084724 Usual severity constipation C0007097 Carcinomas HSDN C0086565 Liver function abnormal C0024586 Malignant carcinoid syndrome MalaCards C4084727 Cough frequency C2931916 Midline granulomatosis MalaCards C0011570 Monopolar depression C0022336 Creutzfeldt-jakob disease MalaCards|HPO C1963064 Anxiety adverse event C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C0003467 Angst C1849158 Insulin-like growth factor i, resistance to, due to increased binding protein HPO C4084726 Distress cough C0027663 Neoplasms, multiple primary HSDN C4084776 Weight loss C0030328 Panniculitis, nodular nonsuppurative OrphaNet|MalaCards C0578994 Bad mouth taste C1282895 Taste, unpleasant, neurologic UMLS C2919142 Short stature adverse event C0796200 Wieacker-wolff syndrome MalaCards C0375546 Heart murmur undiagnosed C0018824 Heart valve disease UMLS C0151786 Weakness muscle C0085278 Antiphospholipid syndrome HSDN C0018681 Headache, cephalalgia C0677866 Brain stem neoplasms HSDN C3146279 Coma C0162557 Liver failure, acute HSDN C4085210 Usual severity pain C1546949 Event consequence - death HSDN C0518090 Frequency of pain question C0027429 Nasal obstruction present finding HSDN C0746674 Muscle weakness generalized C1846343 Bartter syndrome, type 3 MalaCards|HPO|UMLS C0036572 Convulsion C0039685 Tetralogy of fallot HSDN C2096293 Ent surgical result ear vertigo C0270611 Brain damage HSDN C4085862 Bothered by nausea C0013377 Dysgerminoma HSDN C0020903 Illusion C0007786 Brain ischemia HSDN C4084776 Weight loss C0086768 Pancreatic cholera OrphaNet|MalaCards C0011991 Loose stools C0079840 Milk allergy HSDN C1963170 Hypothermia adverse event C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO C3539895 Pelvic pain occurs with bowel movement C0021359 Infertility HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0001883 Airway obstruction HSDN C0005745 Blepharoptosis C1850864 Familial congenital muscular dystrophy with gonadal dysgenesis OrphaNet|MalaCards C4085211 Pain distress question C0497580 Condylomata acuminata in men HSDN C0040822 D tremors C0019159 Hepatitis a HSDN C1549543 Administration method - pain C0028879 Odontogenic cysts HSDN C0004134 Dyssynergia C0008049 Chicken pox HSDN C4084802 Usual severity diarrhea C0003090 Ankylosis HSDN C2024893 Cardiovascular surgery result: fatigue C0079731 B-cell lymphomas HSDN C0022346 Yellow skin C0342443 Adrenal cushing's syndrome HSDN C0086565 Liver function abnormal C1838299 Peroxisome biogenesis disorder, complementation group 14 MalaCards C3463815 Feel fatigue C0015456 Facial dermatoses HSDN C0518090 Frequency of pain question C0039254 Taenia infestation HSDN C0002170 Alopecia disorders C0265205 Robinow syndrome MalaCards C1384666 Decreased hearing C0023786 Mucopolysaccharidosis i OrphaNet C2984057 Have nausea C0010823 Cytomegalovirus infections HSDN C0022346 Yellow skin C1856401 Etfa deficiencies HPO C0747251 Paraparesis spastic progressive C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0018772 Deafness C0032460 Polycystic ovary syndrome HSDN C4084784 Diarrhea C0002878 Anemia, hemolytic HSDN C0010520 Skin cyanosis C1849554 Lymphangiectasia, pulmonary, congenital OrphaNet|MalaCards C0086565 Liver function abnormal C0153460 Malignant neoplasm of tail of pancreas MalaCards C0085593 Chill C0027720 Nephrosis HSDN C0034151 Hyperglobulinemic purpura C0021051 Immunologic deficiency syndromes HSDN C0036572 Convulsion C0024221 Lymphangioma HSDN C1963252 Tremor adverse event C0033922 Psychomotor disorders MalaCards C0020672 Body temperature decreased C1999266 Depression adverse event HSDN C0233844 Awkwardness C0751254 Creutzfeldt-jakob disease, familial MalaCards C4084773 Bothered by weight gain C0311386 Isosporiasis HSDN C0009024 Clonus C4225171 Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration UMLS C0034933 Abnormal reflexes C0042075 Urologic diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C3273031 Hnec MalaCards C0014591 Bleeding nose C3838758 Familial hyperaldosteronism type 3 MalaCards C2984057 Have nausea C0023283 Leishmaniasis, cutaneous HSDN C0424755 Fever symptoms C0740277 Bile duct carcinoma HPO C3641755 Have constipation C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C4084767 Bothered by vomiting C0007137 Squamous cell carcinoma HSDN C0424755 Fever symptoms C0029134 Optic neuritis HSDN C0009792 Consciousness disorder C0027849 Neuroleptic malignant syndrome HSDN C1963170 Hypothermia adverse event C0026946 Mycoses HSDN C0030193 Sense of pain C0041325 Peritonitis, tuberculous MalaCards|HSDN C0036396 Sciatica C3541306 Plasmodium measurement HSDN C0002962 Angina C0242350 Erectile dysfunction HSDN C0030552 Paralysis partial C0011882 Diabetic neuropathies HSDN C1000483 Genus anemia C0017205 Gaucher disease OrphaNet|MalaCards C2911645 Weight loss adverse event C0029001 Onchocerciasis HSDN C0018784 Deafness sensorineural C0085436 Meningitis, cryptococcal HSDN C0013604 Edematous C0600268 Cheilitis granulomatosa MalaCards C3887638 Failure to thrive in infant C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive MalaCards C0020580 Decreased sensation C1860518 Vasculopathy, retinal, with cerebral leukodystrophy HPO C0000737 Abdomen pain C1292753 Primary effusion lymphoma OrphaNet|MalaCards C1069915 Vertigo C0007194 Hypertrophic cardiomyopathy HSDN C0576456 Poor feeding C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C0000737 Abdomen pain C0010340 Critical illness HSDN C3641756 Have diarrhea C0023443 Hairy cell leukemia HSDN C0042571 Vertigo subjective C0520754 Posttraumatic vertigo, nos UMLS C0009792 Consciousness disorder C0038356 Stomach neoplasms HSDN C0020438 Hypercalciuria C0020621 Hypokalemia HSDN C3641755 Have constipation C0034063 Pulmonary edema HSDN C0011168 Disorder deglutition C0342871 Acyl-coa oxidase deficiency MalaCards C0018772 Deafness C2748910 Rett syndrome, atypical OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0243026 Sepsis HSDN C0518090 Frequency of pain question C0206704 Carcinoma, large cell HSDN C1963177 Muscle pain adverse event C1839780 Fragile x tremor/ataxia syndrome MalaCards C1963071 Back pain adverse event C0010346 Crohn disease HSDN C0009806 Constipate C1961100 Erectile dysfunction adverse event HSDN C1963091 Diarrhea adverse event C0030922 Peptic ulcer hemorrhage HSDN C0018772 Deafness C0043241 Wound infection HSDN C0038002 Spleen enlargement C1844376 Granulomatous disease, chronic, x-linked MalaCards|HPO C4085862 Bothered by nausea C0039730 Thalassemia HSDN C0015469 Facial paralysis C0036202 Sarcoidosis MalaCards|HPO C0242936 Center pain C0017185 Gastrointestinal neoplasms HSDN C0008031 Pain chest C0005967 Bone neoplasms HSDN C0522224 Palsied C0024530 Malaria HSDN C0000737 Abdomen pain C0017636 Glioblastoma HSDN C2984058 Have pain C0038358 Gastric ulcer HSDN C4084766 Vomiting C0004030 Aspergillosis HSDN C0231835 Respiration rate increased C0004763 Barrett esophagus HSDN C0037317 Sleep disturbance C0037672 Somnambulism UMLS C0022346 Yellow skin C0854176 Malignant hepato-biliary neoplasm MalaCards C0005745 Blepharoptosis C0265303 Acrocephalopolysyndactyly type iv OrphaNet|MalaCards C4084726 Distress cough C0036400 Scimitar syndrome HSDN C0009080 Finger clubbing C3809651 Infantile liver failure syndrome 2 MalaCards C0040822 D tremors C0751955 Brain infarction HSDN C3463815 Feel fatigue C0021933 Intussusception HSDN C4085548 Usual severity dizziness C0004361 Autogenic therapy HSDN C0312416 Morning sickness C0149573 Structure of posterior inferior cerebellar artery HSDN C0008031 Pain chest C0036341 Schizophrenia HSDN C0033377 Caudal displacement C0344487 Lateral meningocele MalaCards C2911647 Weight gain adverse event C3541306 Plasmodium measurement HSDN C0018681 Headache, cephalalgia C0019294 Hernia, inguinal HSDN C1963170 Hypothermia adverse event C0000786 Spontaneous abortion HSDN C0023530 Leukopenia C2675512 Diamond-blackfan anemia 7 MalaCards C0030193 Sense of pain C1333068 Ccmmt UMLS C0042963 Symptoms vomiting C0002994 Angioedema HSDN C0004134 Dyssynergia C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards|UMLS C0000727 Abdomen acute C0236969 Substance-related disorders HSDN C0085593 Chill C0085426 Gram-positive bacterial infections HSDN C4085211 Pain distress question C0007785 Cerebral infarction HSDN C4084774 Have weight loss C0031350 Pharyngitis HSDN C0037317 Sleep disturbance C1836437 B-cell immunodeficiency, distal limb anomalies, and urogenital malformations MalaCards C4085211 Pain distress question C0019348 Herpes simplex infections HSDN C0015230 Exanthem C0857088 Dry face rash UMLS C4085210 Usual severity pain C0750394 Wbc low HSDN C0750937 Appendicular ataxia C0016719 Friedreich ataxia OrphaNet|HPO C0015672 Decreased energy C1302282 Chromaffin cell neoplasm MalaCards C0034933 Abnormal reflexes C0752127 Spinal cord vascular diseases HSDN C0497247 Blood pressure elevation C2698658 Orofaciodigital syndrome type 1 MalaCards C0233762 Hallucinations auditory C1832903 Migraine, sporadic hemiplegic HPO C0013404 Respiratory difficulty C0023890 Liver cirrhosis HSDN C0036572 Convulsion C0154723 Migraine with aura HSDN C3815497 Cough C0878544 Cardiomyopathies HSDN C0242936 Center pain C0003431 Antisocial personality disorder HSDN C0039070 Collapse fleeting C0019054 Hemolysis (disorder) HSDN C0033377 Caudal displacement C2936917 Infantile polyarteritis MalaCards C1961131 Cough adverse event C0000768 Congenital abnormality HSDN C0042798 Vision dim C1832440 Microphthalmia, syndromic 8 OrphaNet|MalaCards C1963087 Constipation adverse event C1578691 Congenital myxedema MalaCards C0004093 Asthenia C0011581 Depressive disorder HSDN C0848203 Male pelvic pain C0029436 Bone disease, disappearing HSDN C4085211 Pain distress question C0085399 Ehrlichiosis HSDN C0151786 Weakness muscle C0041295 Tuberculoma HSDN C0023012 Delay language C0574080 Guanidinoacetate methyltransferase deficiency MalaCards|HPO C0021359 Infertility C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C4084723 Constipation C0009244 Behavioral cognitive therapy HSDN C0015468 Face pain C0269084 Vulvar vestibulitis HSDN C1963180 Neck pain adverse event C1963138 Hypertension adverse event HSDN C0151818 Opisthotonos C1848526 Pontocerebellar hypoplasia type 2a HPO|UMLS C0015672 Decreased energy C1837218 Cleft palate, isolated HSDN C0242936 Center pain C0039240 Supraventricular tachycardia HSDN C0018681 Headache, cephalalgia C3899674 Childhood brain oligodendroglioma UMLS C1860844 Sparse, thin hair C0220769 Fg syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0025061 Disease of mediastinum HSDN C0003126 Smell loss C1283803 Female kallman syndrome UMLS C0727671 Red cross toothache drops C0009241 Cognition disorders HSDN C4084897 Sleep disturbance subordinate domain C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO C3496180 Sleep apnea C2931196 Craniofacial dysostosis type 1 MalaCards|HPO C0009421 Comatose C0016563 Form perception HSDN C4084897 Sleep disturbance subordinate domain C0040517 Gilles de la tourette syndrome MalaCards|HPO C4085548 Usual severity dizziness C0023895 Liver diseases HSDN C0002965 Crescendo angina C0020542 Pulmonary hypertension HSDN C1963087 Constipation adverse event C0025222 Melena HSDN C0152169 Colic renal C0035357 Retroperitoneal fibrosis HSDN C4084784 Diarrhea C0027858 Neuroma HSDN C0086437 Joint hypermobility C1838625 Warburg sjo fledelius syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0031154 Peritonitis HSDN C1963091 Diarrhea adverse event C0002171 Alopecia areata HSDN C4085317 Diarrhea frequency C0018081 Gonorrhea HSDN C0018772 Deafness C0019189 Hepatitis, chronic HSDN C0034150 Skin purpura C0019693 Hiv infections HSDN C0023014 Developmental disorder language C0013264 Muscular dystrophy, duchenne HSDN C3146279 Coma C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C4084802 Usual severity diarrhea C0029877 Ear inflammation HSDN C0004093 Asthenia C0268450 Gitelman syndrome HSDN C1963091 Diarrhea adverse event C0032987 Ectopic pregnancy HSDN C0007814 Cerebrospinal fluid otorrhea C0078981 Arachnoid cysts HSDN C3539891 Pelvic pain to the rear C0015558 Fallopian tube neoplasms HSDN C4085549 Dizziness C0002878 Anemia, hemolytic HSDN C1963087 Constipation adverse event C1299262 Sarcoma - category (morphologic abnormality) HSDN C1971624 Appetite absent C0036357 Psychology, schizophrenic HSDN C2984058 Have pain C0021831 Intestinal diseases HSDN C4084776 Weight loss C0020598 Hypocalcemia HSDN C0012833 Dizzy C0038587 Substance withdrawal syndrome HSDN C0013421 Dystonia C0037369 Smoking HSDN C0020580 Decreased sensation C0206366 Ossification of posterior longitudinal ligament HSDN C0030486 Extremity paralysis, lower C0001144 Acne vulgaris HSDN C4085211 Pain distress question C0206620 Lymphangioma, cystic HSDN C0002965 Crescendo angina C0017168 Gastroesophageal reflux disease HSDN C3829611 Nausea frequency C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN C0013456 Pain ear C0040997 Trigeminal neuralgia HSDN C3541349 Syncope C0017160 Gastroenteritis HSDN C0003079 Pupillary inequality C0160680 Carotid artery injury HSDN C0042571 Vertigo subjective C1762616 Meningioma, benign, no icd-o subtype HSDN C0009398 Color vision defects C2586211 Thrombosis of blood vessel HSDN C0009806 Constipate C1866927 Smcr HPO C0271215 Blindness legal C2960129 Vanishing white matter disease MalaCards C1549543 Administration method - pain C0037974 Spirochaetales infections HSDN C2237041 Shox gene with short stature C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C3541349 Syncope C2937421 Prostatic hyperplasia HSDN C0015970 Fever unknown origin C0027651 Tumor HSDN C1549543 Administration method - pain C0020635 Hypopituitarism HSDN C1549543 Administration method - pain C0027070 Myoepithelioma HSDN C0015300 Ocular proptosis C0021345 Infectious mononucleosis MalaCards C0221170 Stiffness muscle C4023182 Abnormality of muscle physiology UMLS C0000737 Abdomen pain C0037929 Spinal cord injuries HSDN C2315100 Pediatric failure to thrive C0700095 Central neuroblastoma MalaCards C0015469 Facial paralysis C0004933 Behavior modification technique HSDN C0037771 Paraparesis spastic C0007760 Cerebellar diseases HSDN C3641755 Have constipation C0032963 Pregnancy complications, cardiovascular HSDN C1279888 Proteinuria of undiagnosed cause C0010340 Critical illness HSDN C0013404 Respiratory difficulty C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C0033377 Caudal displacement C0553586 Cafe-au-lait macules with pulmonary stenosis OrphaNet|HPO|MalaCards C0022346 Yellow skin C0034359 Cell pus urine HSDN C0000737 Abdomen pain C3151482 Hypercalciuria, childhood, self-limiting HPO C0240941 Scalp pruritus C1302820 Disorder of skin of head UMLS C0003862 Pain joint C0020517 Hypersensitivity HSDN C0003862 Pain joint C0340992 Cryoglobulinemic; vasculitis OrphaNet|MalaCards C1963071 Back pain adverse event C0009917 Contracture HSDN C1963071 Back pain adverse event C0020625 Hyponatremia HSDN C0242936 Center pain C0014553 Absence epilepsy HSDN C0018784 Deafness sensorineural C0019151 Hepatic encephalopathy HSDN C0043094 Weight gain C2073625 X-ray of chest: pleural effusion HSDN C0015300 Ocular proptosis C2936791 Antley-bixler syndrome, autosomal dominant OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C0221018 Hereditary sideroblastic anemia HSDN C1963071 Back pain adverse event C1134719 Invasive ductal breast carcinoma HSDN C0000737 Abdomen pain C3273047 Perihilar bile duct carcinoma UMLS C3665859 Disturbance of thermoregulation of newborn C0159009 Conditions involving the integument and temperature regulation of fetus and newborn UMLS C1963063 Anorexia adverse event C0030920 Peptic ulcer HSDN C0000727 Abdomen acute C0006663 Calcinosis HSDN C3641756 Have diarrhea C0019360 Herpes zoster disease HSDN C0013404 Respiratory difficulty C0234421 Conscious HSDN C0042963 Symptoms vomiting C0009373 Colonic diseases HSDN C3163620 Hypotension adverse event C0023240 Legionellosis MalaCards C2032396 Pelvic pain on the right C0751792 Trauma, nervous system HSDN C0030193 Sense of pain C0080274 Urinary retention HSDN C0344428 Ventricular tachycardia by ecg finding C3554047 Ventricular tachycardia, catecholaminergic polymorphic, 4 MalaCards C0349588 Stature short C2931570 Duplication 4p syndrome OrphaNet|MalaCards C1963184 Nystagmus adverse event C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome MalaCards C4084788 Have dizziness C0017636 Glioblastoma HSDN C1963281 Vomiting adverse event C1833511 Carnitine palmitoyltransferase ii deficiency, infantile HPO C0040822 D tremors C0005874 Blushing HSDN C0030232 Color loss C0242528 Azotemia HSDN C0497406 Over weight C0009324 Ulcerative colitis HSDN C4084726 Distress cough C0034530 Injury radiation HSDN C3539896 Pelvic pain occurs with urination C0016664 Fatigue fracture HSDN C0010200 Cough symptom C1336145 Stage ib squamous cell lung carcinoma UMLS C1961131 Cough adverse event C1963084 Colitis adverse event HSDN C1145670 Failure respiratory C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C4085211 Pain distress question C0015347 Extinction HSDN C0242936 Center pain C3495801 Granulomatosis with polyangiitis HSDN C0004941 Behavioral symptoms C1850985 Fragile site 16p12 HPO C4084788 Have dizziness C0042373 Vascular diseases HSDN C3274924 Have been coughing C0242698 Ventricular dysfunction, left HSDN C0002962 Angina C0039131 Syphilis congenital HSDN C3898969 Have been vomiting C0036220 Kaposi sarcoma HSDN C0018524 Hallucinate C1565106 Headache disorders, primary HSDN C0036572 Convulsion C4225320 Congenital disorder of glycosylation, type iz UMLS C4084723 Constipation C0812393 Cancer patients and suicide and depression HSDN C3539895 Pelvic pain occurs with bowel movement C1546602 Specimen source codes - diverticulum HSDN C0005745 Blepharoptosis C1855675 Arima syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0161398 Neuropathy optic traumatic HSDN C2984057 Have nausea C0027686 Pathologic neovascularization HSDN C0030975 Disorders perception C0079487 Helicobacter infections HSDN C0035229 Respiratory function impaired C1863389 Apert-crouzon disease MalaCards C0003962 Ascites C2931167 Maternofetal infection by parvovirus OrphaNet|MalaCards C1557397 Adverse event associated with pain C0009766 Allergic conjunctivitis HSDN C1069915 Vertigo C3812171 Bradycardia by ecg finding HSDN C2919142 Short stature adverse event C1845168 Hypophosphatemic rickets, x-linked recessive MalaCards|HPO C0520909 Ponv C0040799 Traumatic subcutaneous emphysema HSDN C2315100 Pediatric failure to thrive C0268630 Hyper-beta-alaninemia MalaCards C0040034 Thrombocytopenia C3554330 Nephrotic syndrome, type 7 MalaCards C4085661 Usual severity nausea C0011581 Depressive disorder HSDN C0424755 Fever symptoms C0004044 Asphyxia HSDN C0151889 Reflexes tendon increased C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C2911645 Weight loss adverse event C0006261 Bronchial diseases HSDN C0423658 Arthralgia of the ankle and foot C2702829 Compression arthralgia of right ankle or foot UMLS C0010200 Cough symptom C0270611 Brain damage HSDN C4085211 Pain distress question C0030100 Oxyuriasis HSDN C0030193 Sense of pain C0024138 Lupus erythematosus, discoid HSDN C0019825 Voice hoarseness C0036391 Schwartz-jampel syndrome MalaCards|HPO C4085211 Pain distress question C1963107 Euphoria adverse event HSDN C0037317 Sleep disturbance C0008628 Chromosome deletion MalaCards C4085210 Usual severity pain C0038531 Subclavian artery stenosis HSDN C0010200 Cough symptom C0917875 Esophageal diverticulosis HSDN C0013604 Edematous C0003507 Aortic valve stenosis HSDN C2364082 Hyposmia C0162809 Kallmann syndrome OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C1263846 Attention deficit hyperactivity disorder HSDN C0019209 Large liver C1856492 Gaucher disease, type iiib HPO C0037317 Sleep disturbance C3150756 Chromosome 4q21 deletion syndrome MalaCards C2911647 Weight gain adverse event C0025521 Inborn errors of metabolism HSDN C0039070 Collapse fleeting C0024141 Lupus erythematosus, systemic HSDN C0038990 Sweats C1850568 Nakajo syndrome MalaCards C4084768 Usual severity vomiting C0021603 Sleep initiation and maintenance disorders HSDN C0795692 Lactate blood increased C2752074 Alpha-ketoglutarate dehydrogenase deficiency MalaCards C0426579 Anorexia symptom C0020437 Hypercalcemia HSDN C4085210 Usual severity pain C0039082 Syndrome HSDN C0015672 Decreased energy C0342257 Complications of diabetes mellitus HSDN C0518090 Frequency of pain question C0020524 Disorders of excessive somnolence HSDN C0023380 Lethargy C2960129 Vanishing white matter disease MalaCards C1384666 Decreased hearing C4085311 Depression - recess HSDN C4084774 Have weight loss C1366464 F9 gene HSDN C0242936 Center pain C0023676 Life style HSDN C0497247 Blood pressure elevation C0268389 Amyloidosis, familial visceral MalaCards|HPO C0151686 Growth retardation C3280538 Mental retardation, autosomal recessive 27 MalaCards C2203646 Jaundice C0006109 Brain damage, chronic HSDN C4085210 Usual severity pain C0019187 Hepatitis, alcoholic HSDN C0036572 Convulsion C0751304 Meningioma, parasagittal UMLS C0018991 Paralysis one side of body C0751434 Classical phenylketonuria MalaCards|HPO C3463815 Feel fatigue C0038358 Gastric ulcer HSDN C0522224 Palsied C0029896 Disease, ent HSDN C4084774 Have weight loss C0206138 Crest syndrome MalaCards C0013362 Dysarthrias C0376532 Epilepsy, rolandic HSDN C0042571 Vertigo subjective C0037937 Spine injury HSDN C1963093 Dizziness adverse event C3810814 Myocardial infarction ecg assessment HSDN C0242936 Center pain C0020507 Hyperplasia HSDN C0521800 Central cyanosis C0272088 Haemoglobinopathy with cyanosis, nos UMLS C1963065 Apnea adverse event C4015710 Tenorio syndrome MalaCards C3887638 Failure to thrive in infant C1864871 Chromosome 17q21.31 deletion syndrome MalaCards|HPO C0015469 Facial paralysis C0162871 Aortic aneurysm, abdominal HSDN C0018784 Deafness sensorineural C1832978 Deafness, autosomal recessive 7 MalaCards|HPO C0151818 Opisthotonos C0342765 D-glyceric aciduria HPO|UMLS C0040822 D tremors C2751067 Parkinsonism-dystonia, infantile MalaCards|HPO|UMLS C3539891 Pelvic pain to the rear C0033046 Premenstrual syndrome HSDN C0023530 Leukopenia C1859534 Bare lymphocyte syndrome, type ii, complementation group a HPO C0518090 Frequency of pain question C0014378 Enterovirus infections HSDN C3539891 Pelvic pain to the rear C0085222 Psoas muscle abscess HSDN C0030193 Sense of pain C0014335 Enteritis HSDN C0242936 Center pain C0035920 Rubella HSDN C0013421 Dystonia C3150705 Foxg1 syndrome HPO C0018681 Headache, cephalalgia C2931270 Craniodiaphyseal dysplasia, dominant MalaCards C4085317 Diarrhea frequency C0032227 Pleural effusion disorder HSDN C0007758 Cerebellar ataxia C0268608 Deficiency of dihydrofolate reductase MalaCards C0042024 Urine incontinence C0004161 Athletic injuries HSDN C0018772 Deafness C1546847 Entity name part type - family HSDN C0151786 Weakness muscle C3541306 Plasmodium measurement HSDN C0010520 Skin cyanosis C0004245 Atrioventricular block HSDN C4085862 Bothered by nausea C0020443 Hypercholesterolemia HSDN C0042571 Vertigo subjective C0004935 Animal ethology HSDN C0018777 Deafness, conductive C0406709 Hay-wells syndrome HPO C0349588 Stature short C1332140 Acrofacial dysostosis MalaCards C0151786 Weakness muscle C0034186 Pyelonephritis HSDN C2237041 Shox gene with short stature C1836437 B-cell immunodeficiency, distal limb anomalies, and urogenital malformations MalaCards C3641753 Lacks appetite C0276357 Swine influenza MalaCards C4084773 Bothered by weight gain C0242339 Dyslipidemias HSDN C3714552 Strength decreased C0268060 Juvenile hemochromatosis MalaCards C1963086 Confusion adverse event C0014038 Encephalitis HSDN C4085211 Pain distress question C0024525 Malacoplakia HSDN C0042963 Symptoms vomiting C0032320 Peritoneal free air HSDN C0454644 Delayed language development C1867858 Prader-willi syndrome chromosome region HPO C4084802 Usual severity diarrhea C0026636 Mouth diseases HSDN C0010200 Cough symptom C0025286 Meningioma HSDN C0030486 Extremity paralysis, lower C0015480 Disorder factitious HSDN C0018681 Headache, cephalalgia C0338486 Accompaniments migraine UMLS C0522224 Palsied C0206247 Amyloid neuropathies HSDN C0026826 High muscle tone C1866425 Yemenite deaf-blind hypopigmentation syndrome MalaCards C4085211 Pain distress question C0034041 Puerperal infection HSDN C0018784 Deafness sensorineural C0037277 Skin diseases, genetic HSDN C4085211 Pain distress question C0020524 Disorders of excessive somnolence HSDN C3665347 Vision impaired C0265303 Acrocephalopolysyndactyly type iv MalaCards C0010200 Cough symptom C1333123 Combined carcinoma of lung UMLS C4084775 Usual severity weight loss C1263846 Attention deficit hyperactivity disorder HSDN C0027796 Neuralgias C0442874 Neuropathy UMLS C3898969 Have been vomiting C0003869 Arthritis, infectious HSDN C0751837 Gait ataxic C1335712 Medulloblastoma recurrent UMLS C4085317 Diarrhea frequency C0398691 Hyperimmunoglobulinemia d OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C1319688 Blister dose form HSDN C1963071 Back pain adverse event C0520946 Emotional hypersensitivity HSDN C1549543 Administration method - pain C0043253 Trauma blunt HSDN C0575081 Abnormal gait C0013364 Dysautonomia, familial OrphaNet|HPO C4084723 Constipation C0038661 Suicide HSDN C0036572 Convulsion C1332610 Brain stem glioblastoma UMLS C0037763 Spasm C0034530 Injury radiation HSDN C0002965 Crescendo angina C0032914 Pre-eclampsia HSDN C0027796 Neuralgias C0039984 Thoracic outlet syndrome HSDN C3274924 Have been coughing C0004031 Aspergillosis, allergic bronchopulmonary DiseaseOntology|OrphaNet|MalaCards C0009269 Cold intolerance C0027145 Myxedema MalaCards C0030193 Sense of pain C0019556 Canine hip dysplasia HSDN C4084784 Diarrhea C0018794 Heart block HSDN C0030554 Abnormal sensation C0029172 Oral submucous fibrosis HSDN C0917816 Deficiency mental C0276496 Familial alzheimer disease (fad) MalaCards C1963090 Dehydration adverse event C1565489 Renal insufficiency MalaCards C1557397 Adverse event associated with pain C0717360 Disease lyme vaccine HSDN C0036572 Convulsion C0004106 Astigmatism HSDN C1961131 Cough adverse event C0236969 Substance-related disorders HSDN C0043094 Weight gain C0019156 Hepatic veno-occlusive disease OrphaNet|MalaCards C0242936 Center pain C0025294 Meningococcal meningitis HSDN C0424755 Fever symptoms C0344434 Atrial fibrillation ecg HSDN C1963071 Back pain adverse event C0812393 Cancer patients and suicide and depression HSDN C0700590 Diaphoresis excessive C1956391 Temporal arteritis MalaCards|HPO C4084802 Usual severity diarrhea C1565489 Renal insufficiency HSDN C0393588 Dystonias paroxysmal C1290841 Acute disease of nervous system UMLS C0010200 Cough symptom C0235833 Congenital diaphragmatic hernia HSDN C0162835 Hypopigmentation C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0000737 Abdomen pain C0279643 Undifferentiated carcinoma of colon UMLS C0015672 Decreased energy C0034951 Refractive errors HSDN C0877627 Dysaesthesia of tongue C0006430 Burning mouth syndrome UMLS C0037763 Spasm C0011570 Mental depression HSDN C4084769 Vomiting frequency C0405580 Adrenal cortical hypofunction HSDN C0557874 Global developmental delay C1867775 Sacral agenesis, hereditary, with presacral mass, anterior meningocele, and-or teratoma, and anorectal malformation HPO C0022346 Yellow skin C1856405 Glutaric aciduria iic HPO C3829611 Nausea frequency C1704326 Role - roleclass HSDN C0007758 Cerebellar ataxia C1864669 Neuronal ceroid lipofuscinosis due to cathepsin d deficiency MalaCards|HPO C0917816 Deficiency mental C2718068 Beta-galactosidase deficiency MalaCards C0043094 Weight gain C0038661 Suicide HSDN C4085210 Usual severity pain C0428478 Serum triglycerides raised HSDN C1962972 Proteinuria adverse event C0848377 Trauma to the abdomen HSDN C0013604 Edematous C0042214 Vaccinia HSDN C4085210 Usual severity pain C0020507 Hyperplasia HSDN C0000737 Abdomen pain C1384600 Systemic onset juvenile chronic arthritis MalaCards|HPO C0015469 Facial paralysis C1306577 Dies patient HSDN C1557397 Adverse event associated with pain C0022423 Judgement HSDN C4085210 Usual severity pain C0024954 Maxillary neoplasms HSDN C0024031 Back pain lower back C0027663 Neoplasms, multiple primary HSDN C4084724 Usual severity constipation C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO C0857305 Thrombocytopenia purpura C0011854 Diabetes mellitus, insulin-dependent HSDN C0020672 Body temperature decreased C0018133 Graft-vs-host disease HSDN C3887638 Failure to thrive in infant C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards|HPO C2029884 Hearing loss by exam C0023269 Leiomyosarcoma HSDN C0026205 Pupillary constriction C0997768 Glaucoma HSDN C0036572 Convulsion C1562503 Vein of galen malformations HSDN C0522224 Palsied C1963198 Pancreatitis adverse event HSDN C3887638 Failure to thrive in infant C1836033 Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome MalaCards|HPO C0085602 Polydypsia C0022976 Animal gait disorder HSDN C0030552 Paralysis partial C0027813 Neuritis HSDN C3463815 Feel fatigue C0043194 Wiskott-aldrich syndrome OrphaNet|HPO|MalaCards C4084774 Have weight loss C0021295 Infant, premature, diseases HSDN C0020450 Hyperemesis gravidarum C0019159 Hepatitis a HSDN C0851578 Disorder sleep C0032019 Pituitary neoplasms HSDN C1963184 Nystagmus adverse event C0155299 Coloboma of optic disc MalaCards C0010200 Cough symptom C0018939 Hematological disease HSDN C0005758 Blister C0149781 Spontaneous pneumothorax MalaCards C4084802 Usual severity diarrhea C0020523 Immediate hypersensitivity HSDN C0040822 D tremors C2981150 Uranostaphyloschisis HSDN C4084775 Usual severity weight loss C0039590 Testicular neoplasms HSDN C0019079 Bloody sputum C0014860 Perforation esophagus HSDN C1279888 Proteinuria of undiagnosed cause C0036974 Shock HSDN C2096293 Ent surgical result ear vertigo C0014055 Encephalitis, epidemic HSDN C0027498 Nausea vomiting C0038325 Stevens-johnson syndrome OrphaNet|HPO C1963091 Diarrhea adverse event C0003090 Ankylosis HSDN C0036572 Convulsion C0029401 Osteitis deformans HSDN C0009763 Conjunctiva inflammation C1850568 Nakajo syndrome MalaCards|HPO C0000737 Abdomen pain C1333867 Grade 1 colorectal adenocarcinoma UMLS C0018681 Headache, cephalalgia C0700201 Dyssomnias HSDN C1962972 Proteinuria adverse event C0517555 Venous thrombosis after immobility HSDN C0700590 Diaphoresis excessive C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0015402 Hemorrhage eye C0027092 Myopia HSDN C4084727 Cough frequency C0302148 Blood clot HSDN C0241210 Speaking delay C2750234 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 MalaCards|HPO C0026838 Spasticity muscle C1864669 Neuronal ceroid lipofuscinosis due to cathepsin d deficiency MalaCards|HPO|UMLS C0036572 Convulsion C0036980 Shock, cardiogenic HSDN C0349489 Fetal hypoxia C0002351 Altitude sickness HSDN C0002622 Amnesias C1962979 Burn adverse event HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0036749 Serositis HSDN C0038506 Stutter C0006118 Brain neoplasms HSDN C0242936 Center pain C0010606 Adenoid cystic carcinoma HSDN C0018681 Headache, cephalalgia C0040034 Thrombocytopenia UMLS C4084774 Have weight loss C0040128 Thyroid diseases HSDN C0024032 Birth weight subnormal C3542022 Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome MalaCards C3641756 Have diarrhea C0014805 Primary erythermalgia MalaCards|HPO C0162298 Stiffness joints C1864356 Acromesomelic dysplasia, maroteaux type OrphaNet|HPO|MalaCards C2984057 Have nausea C0032285 Pneumonia HSDN C4084725 Usual severity cough C0021390 Inflammatory bowel diseases HSDN C3274924 Have been coughing C2609414 Acute kidney injury HSDN C0016199 Pain flank C2609414 Acute kidney injury HSDN C0036572 Convulsion C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C0019214 Hepatosplenomegaly C0030297 Pancreatic neoplasm MalaCards C0030193 Sense of pain C0034063 Pulmonary edema HSDN C0242936 Center pain C1555914 Psychologist - psychotherapy, group HSDN C4085211 Pain distress question C0036240 Response, satiety HSDN C0003862 Pain joint C1299262 Sarcoma - category (morphologic abnormality) HSDN C0030552 Paralysis partial C0033975 Psychotic disorders HSDN C0000786 Abortion spontaneous C3463916 Complement factor i (c3 inactivator) deficiency MalaCards C0023012 Delay language C3150924 Mental retardation, anterior maxillary protrusion, and strabismus MalaCards|HPO C4084724 Usual severity constipation C0236969 Substance-related disorders HSDN C0751093 Dystonia, limb C1867983 Porencephaly, familial HPO|UMLS C0424755 Fever symptoms C0006264 Bronchial neoplasms HSDN C3887873 Hearing loss C0011265 Presenile dementia HSDN C0231218 Malaise generalized C1513718 Mucin-producing intrahepatic cholangiocarcinoma UMLS C0026826 High muscle tone C0024591 Malignant hyperpyrexia due to anesthesia HSDN C0241210 Speaking delay C1847522 Momes syndrome MalaCards C0026838 Spasticity muscle C1856973 Encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration OrphaNet|MalaCards C0522224 Palsied C2186740 Reported urticaria HSDN C0015402 Hemorrhage eye C0037033 Necrotizing sialometaplasia HSDN C4085661 Usual severity nausea C0004364 Autoimmune diseases HSDN C0424790 Chill shaking C0694549 Community acquired pneumonia UMLS C0349588 Stature short C3489726 Geleophysic dysplasia MalaCards C4085862 Bothered by nausea C0029456 Osteoporosis HSDN C0003910 Articulation disorder C0010266 Cranial nerve diseases HSDN C2911645 Weight loss adverse event C0040948 Trichostrongyliasis HSDN C0349588 Stature short C1859773 Microphthalmia, syndromic 3 MalaCards|HPO C0042571 Vertigo subjective C0021799 Interprofessional relations HSDN C4084766 Vomiting C0023903 Liver neoplasms HSDN C0018772 Deafness C2586211 Thrombosis of blood vessel HSDN C0007758 Cerebellar ataxia C0024776 Maple syrup urine disease OrphaNet|HSDN|HPO C2911645 Weight loss adverse event C0036220 Kaposi sarcoma HSDN C0020673 Hypothermia (central) (local) C0302148 Blood clot HSDN C0038990 Sweats C0206042 Fatal familial insomnia HPO C0349588 Stature short C1969057 Noonan syndrome 5 MalaCards|HPO C1557397 Adverse event associated with pain C0019066 Nontraumatic hemoperitoneum HSDN C2911647 Weight gain adverse event C0085183 Neoplasms, second primary HSDN C2984058 Have pain C0853697 Neutrophil count decreased HSDN C1963281 Vomiting adverse event C0206171 Community acquired infections HSDN C0007398 Catatonic C0236792 Asperger syndrome HSDN C0013390 Cramps menstrual C0028949 Oligomenorrhea HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0585442 Osteosarcoma of bone HSDN C0241137 Skin pallor C0003838 Arterial occlusive diseases HSDN C0024031 Back pain lower back C3887650 Adult rickets HSDN C3641756 Have diarrhea C0010674 Cystic fibrosis HSDN C2203646 Jaundice C0001144 Acne vulgaris HSDN C3641756 Have diarrhea C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C0013404 Respiratory difficulty C0029436 Bone disease, disappearing HSDN C0013421 Dystonia C1527348 Brain hypoxia HSDN C0002962 Angina C1134719 Invasive ductal breast carcinoma HSDN C4084768 Usual severity vomiting C0031039 Effusion pericardial HSDN C0751840 Pure alexia C0023524 Leukoencephalopathy, progressive multifocal HSDN C0031315 Phantom limb pain C3810814 Myocardial infarction ecg assessment HSDN C4084766 Vomiting C0042018 Urinary calculi HSDN C1963071 Back pain adverse event C0006264 Bronchial neoplasms HSDN C0000737 Abdomen pain C1332250 Ampulla of vater small cell carcinoma UMLS C2984058 Have pain C0042995 Vulvar neoplasms HSDN C0041834 Erythematous condition C0042111 Urticaria pigmentosa MalaCards|HPO C1557397 Adverse event associated with pain C0872996 Q fever vaccine HSDN C0009398 Color vision defects C0008525 Choroideremia HSDN C3815497 Cough C0003811 Cardiac arrhythmia HSDN C0026826 High muscle tone C3537048 Trisomy 18 MalaCards C1961131 Cough adverse event C0009375 Colonic neoplasms HSDN C0344315 Mood depressed C0268425 Alstrom syndrome MalaCards|HPO C3887638 Failure to thrive in infant C3150802 Myopathy, lactic acidosis, and sideroblastic anemia 2 MalaCards|HPO C2237041 Shox gene with short stature C0162809 Kallmann syndrome OrphaNet|HPO C0028738 Nystagmus C1855128 Methylcobalamin deficiency, cblg type MalaCards|HPO C0476250 Head neck mass C1290118 Melanocytic naevus of face UMLS C0034933 Abnormal reflexes C0013363 Dysautonomia HSDN C0018681 Headache, cephalalgia C0334419 Pheochromocytoma, malignant UMLS C3814874 Loss of appetite question C0085293 Hepatitis e MalaCards C4084723 Constipation C0037997 Splenic diseases HSDN C1963090 Dehydration adverse event C1855109 Methylmalonic aciduria cbla type HPO C0011206 Delirium acute C1258104 Diffuse scleroderma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007140 Carcinosarcoma HSDN C0040822 D tremors C0270855 Early myoclonic encephalopathy MalaCards C1962972 Proteinuria adverse event C2984291 Glioblastoma multiforme pathway HSDN C0028738 Nystagmus C2673874 Bardet biedl syndrome 14 (disorder) HPO C0033774 Skin pruritus C0241158 Cicatrix skin HSDN C0007859 Pain neck C1546847 Entity name part type - family HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011848 Diabetes insipidus HSDN C1963091 Diarrhea adverse event C0198632 Pneumoperitoneum HSDN C0036572 Convulsion C0234545 Delirium postseizure UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0009376 Colonic polyps HSDN C4084726 Distress cough C0004935 Animal ethology HSDN C3898969 Have been vomiting C0019243 Angioedemas, hereditary HPO C0454644 Delayed language development C3808397 Cortical dysplasia, complex, with other brain malformations 1 MalaCards C0033774 Skin pruritus C0016867 Furunculosis HSDN C0023015 Language handicap C0011269 Dementia, vascular HSDN C0332573 Macula C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C4085210 Usual severity pain C0015670 Child father HSDN C0008031 Pain chest C0524620 Metabolic syndrome x HSDN C1279888 Proteinuria of undiagnosed cause C0011265 Presenile dementia HSDN C4085211 Pain distress question C0025209 Melanosis HSDN C0242936 Center pain C1009209 Tinea HSDN C0413252 Hypothermia due to exposure C0006109 Brain damage, chronic HSDN C0026884 Muteness C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C3829611 Nausea frequency C0018799 Heart diseases HSDN C0015468 Face pain C0027051 Myocardial infarction HSDN C1384666 Decreased hearing C0040136 Thyroid neoplasm HSDN C4085317 Diarrhea frequency C0221056 Adult type dermatomyositis HSDN C2315100 Pediatric failure to thrive C1856303 Gsd iv, neuromuscular form, fatal perinatal HPO C2096293 Ent surgical result ear vertigo C0039494 Temporomandibular joint disorders HSDN C4085317 Diarrhea frequency C0019348 Herpes simplex infections HSDN C4085210 Usual severity pain C0085423 Gram-negative bacterial infections HSDN C4084776 Weight loss C0017638 Glioma HSDN C4084724 Usual severity constipation C0033975 Psychotic disorders HSDN C0151786 Weakness muscle C0024630 Malingering HSDN C1963249 Tinnitus adverse event C0012817 Diverticulum HSDN C0518090 Frequency of pain question C0014548 Epilepsy, generalized HSDN C3274924 Have been coughing C1864997 Majeed syndrome MalaCards|HPO C0040485 Wryneck C0043145 Whiplash HSDN C1836296 Lower extremity weakness C2931355 Spastic paraplegia 3, autosomal dominant HPO|UMLS C2024893 Cardiovascular surgery result: fatigue C0812393 Cancer patients and suicide and depression HSDN C0232950 Menstruation, vicarious C0025345 Menstruation disturbances UMLS C2911645 Weight loss adverse event C0009240 Cognition HSDN C0019079 Bloody sputum C0018809 Heart neoplasm HSDN C0030552 Paralysis partial C0035127 Cumulative trauma disorders HSDN C0009421 Comatose C0012746 Dissociative disorder HSDN C0024031 Back pain lower back C0010340 Critical illness HSDN C0004134 Dyssynergia C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards|UMLS C3539889 Pelvic pain increasing in severity C0012979 Canine disease HSDN C1963252 Tremor adverse event C0037744 Perceptual spatial orientation HSDN C4085210 Usual severity pain C0037322 Active eye movement sleep HSDN C0010200 Cough symptom C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C0023015 Language handicap C0033906 Psychological theories HSDN C0009806 Constipate C0016807 Functional bowel disorder UMLS C0020672 Body temperature decreased C0024299 Lymphoma HSDN C0013144 Drowsy C0011226 Hepatitis d infection DiseaseOntology|MalaCards C3539895 Pelvic pain occurs with bowel movement C0041952 Uerterolithiasis HSDN C4085549 Dizziness C0023448 Lymphoid leukemia HSDN C0020673 Hypothermia (central) (local) C0020488 Hypernatremia HSDN C1963137 Hydrocephalus adverse event C1835912 Aicardi-goutieres syndrome 4 MalaCards|HPO C4085661 Usual severity nausea C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0557874 Global developmental delay C1846421 Lathosterolosis OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0006309 Brucellosis HSDN C0018784 Deafness sensorineural C0751038 Cockayne syndrome, type ii HPO C0857305 Thrombocytopenia purpura C0009375 Colonic neoplasms HSDN C3887873 Hearing loss C1855652 Fetus small for gestational age HSDN C0003862 Pain joint C0038454 Cerebrovascular accident HSDN C1145670 Failure respiratory C0017205 Gaucher disease MalaCards C0007939 Syphilis chancre C0740689 Infect_nos problem UMLS C4085210 Usual severity pain C0036039 Sadism HSDN C0039070 Collapse fleeting C2015933 Outcomes otolaryngology hearing HSDN C4085641 Level of joint pain C0276289 Zika virus infection MalaCards C0018926 Emesis bloody C0025202 Melanoma HSDN C1962972 Proteinuria adverse event C0997768 Glaucoma HSDN C0022346 Yellow skin C0001824 Agranulocytosis HSDN C0033774 Skin pruritus C0020503 Hyperparathyroidism, secondary HSDN C0231785 Spasm carpopedal C0020598 Hypocalcemia UMLS C3815497 Cough C0032131 Plasmacytoma HSDN C0030193 Sense of pain C0012746 Dissociative disorder HSDN C0039070 Collapse fleeting C0022665 Kidney neoplasm HSDN C0344434 Atrial fibrillation ecg C3279693 Atrial fibrillation, familial, 11 MalaCards C3641756 Have diarrhea C0740340 Amyloidosis, familial HSDN C0042571 Vertigo subjective C0155501 Vertigo, peripheral UMLS C0023380 Lethargy C0812393 Cancer patients and suicide and depression HSDN C0221232 Welts C1276117 Episodic idiopathic urticaria UMLS C0030218 Palatal paralysis C1290785 Palatal disorder UMLS C0233565 Bradykinesia C2750220 Karak syndrome MalaCards|HPO C0036572 Convulsion C1864690 Microphthalmia, syndromic 5 MalaCards|HPO|UMLS C1963281 Vomiting adverse event C0033860 Psoriasis HSDN C0011991 Loose stools C0085437 Meningitis, bacterial HSDN C4084802 Usual severity diarrhea C0149721 Left ventricular hypertrophy HSDN C0018772 Deafness C0035204 Respiration disorders HSDN C0018524 Hallucinate C0041948 Uremia HSDN C0242936 Center pain C0027707 Nephritis, interstitial HSDN C3641755 Have constipation C0037928 Spinal cord diseases HSDN C0007758 Cerebellar ataxia C0494451 Cerebellar ataxia with defective dna repair UMLS C3815497 Cough C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C4085661 Usual severity nausea C0030920 Peptic ulcer HSDN C0024031 Back pain lower back C0150277 Meditations HSDN C0015469 Facial paralysis C0162526 Aids-related opportunistic infections HSDN C1963093 Dizziness adverse event C1962963 Osteoporosis adverse event HSDN C0013604 Edematous C0031039 Effusion pericardial HSDN C0424755 Fever symptoms C0003811 Cardiac arrhythmia HSDN C0086565 Liver function abnormal C1833511 Carnitine palmitoyltransferase ii deficiency, infantile HPO C0518090 Frequency of pain question C0025048 Meconium aspiration syndrome HSDN C0423707 Lateral femoral cutaneous neuralgia C3662005 Neuropathy of lower limb UMLS C0027796 Neuralgias C0017638 Glioma HSDN C4085211 Pain distress question C0085215 Ovarian failure, premature HSDN C2362324 Pediatric obesity C0525042 Feeding and eating disorders of childhood HSDN C3815497 Cough C0021841 Intestinal neoplasms HSDN C0520966 Coordination impaired C0175702 Williams syndrome MalaCards|HPO C2911647 Weight gain adverse event C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C3887873 Hearing loss C1548578 Location characteristic id - smoking HSDN C4085211 Pain distress question C0014548 Epilepsy, generalized HSDN C0206146 Myocardial stunning C0600519 Ventricular remodeling HSDN C0018965 Blood urine C0017205 Gaucher disease MalaCards C0033790 Pseudobulbar palsy C0024534 Malaria, cerebral HSDN C4084766 Vomiting C1548777 Specimen reject reason - hemolysis HSDN C2237041 Shox gene with short stature C1864100 Pseudohypoparathyroidism, type ib OrphaNet|HPO|MalaCards C0018834 Brash C0017168 Gastroesophageal reflux disease MalaCards|UMLS C4085222 Nausea C1847839 Episodic ataxia, type 3 MalaCards C0022346 Yellow skin C0020542 Pulmonary hypertension HSDN C0518090 Frequency of pain question C0029888 Otitis media purulent HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018817 Atrial septal defects HSDN C0152116 Torticollis spasmodic C1834570 Myoclonic dystonia HPO C0917816 Deficiency mental C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO C0012833 Dizzy C0001883 Airway obstruction HSDN C0040259 Tinea pedis C0006849 Oral candidiasis HSDN C0013421 Dystonia C1847501 Glut1 deficiency syndrome OrphaNet|MalaCards C1963064 Anxiety adverse event C3683846 Chromosome 17p deletion syndrome MalaCards C0426579 Anorexia symptom C0041351 Tularemia HSDN C0018784 Deafness sensorineural C0039093 Congenital abnormal synostosis HSDN C0005745 Blepharoptosis C1836287 Cerebrorenodigital syndrome with limb malformations and triradiate acetabula OrphaNet|MalaCards C0040034 Thrombocytopenia C0018854 Gamma-chain disease MalaCards C0423658 Arthralgia of the ankle and foot C2105258 Compression arthralgia of ankle or foot UMLS C4084766 Vomiting C0004114 Astrocytoma HSDN C4084723 Constipation C0037019 Shy-drager syndrome HSDN C3898969 Have been vomiting C0029456 Osteoporosis HSDN C0020455 Hypergammaglobulinemia C1961835 Gaucher disease, type 1 MalaCards|HPO C4050613 Anxiety C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C4084802 Usual severity diarrhea C0376634 Craniofacial abnormalities HSDN C2911645 Weight loss adverse event C0031090 Periodontal diseases HSDN C0042928 Paralysis vocal cord C0021400 Influenza HSDN C0454644 Delayed language development C2931325 Chromosome 22 ring MalaCards C2911647 Weight gain adverse event C0022806 Kwashiorkor HSDN C0151889 Reflexes tendon increased C1274789 Ligneous conjunctivitis MalaCards|HPO C4084769 Vomiting frequency C0021845 Intestinal perforation HSDN C0023014 Developmental disorder language C0022661 Kidney failure, chronic HSDN C0587047 Mass of trunk C0431598 Hamartoma liver UMLS C0042963 Symptoms vomiting C0016053 Fibromyalgia HSDN C0427068 Legs weakness C0025286 Meningioma MalaCards C4085211 Pain distress question C0035258 Restless legs syndrome HSDN C0002962 Angina C0679360 Foodborne disease HSDN C0036572 Convulsion C3495025 Typical absence seizure, intractable UMLS C0009421 Comatose C0023055 Laryngeal neoplasm HSDN C2096293 Ent surgical result ear vertigo C0003850 Arteriosclerosis HSDN C0002965 Crescendo angina C0008370 Cholestasis HSDN C2024878 Cardiovascular surgery result: dyspnea C0007138 Carcinoma, transitional cell HSDN C0000727 Abdomen acute C1963274 Vasculitis adverse event HSDN C0424755 Fever symptoms C0085693 Acute appendicitis nos (disorder) MalaCards C4085549 Dizziness C0017178 Gastrointestinal diseases HSDN C4084784 Diarrhea C1552527 Clinic / center - developmental disabilities HSDN C4085210 Usual severity pain C0237104 Spirituality HSDN C0004134 Dyssynergia C0032897 Prader-willi syndrome OrphaNet|MalaCards C2315100 Pediatric failure to thrive C1865644 Plantar lipomatosis, unusual facies, and developmental delay MalaCards|HPO C2036534 Stuttering improved C0038506 Stuttering UMLS C4085317 Diarrhea frequency C0019080 Hemorrhage HSDN C0018775 Hearing loss bilateral C0041327 Tuberculosis, pulmonary HSDN C3539890 Pelvic pain causes awakening at night C2586211 Thrombosis of blood vessel HSDN C0004604 Pain back C0037313 Sleep HSDN C0349588 Stature short C1856929 Epilepsy telangiectasia OrphaNet|MalaCards C0036572 Convulsion C0270840 Complex partial seizures evolving to generalized tonic-clonic seizures UMLS C0030975 Disorders perception C0037650 Somatoform disorder HSDN C4084767 Bothered by vomiting C0006147 Breast fed HSDN C0009398 Color vision defects C0796561 Melanoma vaccines HSDN C4085548 Usual severity dizziness C0013364 Dysautonomia, familial HSDN C2911647 Weight gain adverse event C0027059 Myocarditis HSDN C1963065 Apnea adverse event C0020456 Hyperglycemia HSDN C2919142 Short stature adverse event C1861129 Takao vcf syndrome HPO C0242936 Center pain C0042961 Intestinal volvulus HSDN C0237849 Skin desquamation C1862005 Epidermolytic hyperkeratosis, late-onset HPO C0015672 Decreased energy C0007785 Cerebral infarction HSDN C0424755 Fever symptoms C0007131 Non-small cell lung carcinoma HSDN C0413252 Hypothermia due to exposure C0151814 Coronary occlusion HSDN C4084802 Usual severity diarrhea C2020541 Strabismus HSDN C0518090 Frequency of pain question C0042065 Genitourinary neoplasms HSDN C0221752 Rbc urine C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C0033774 Skin pruritus C4023527 Abnormality of skin physiology UMLS C0015230 Exanthem C0343206 Hypocomplementemic urticarial vasculitis MalaCards C4085549 Dizziness C0042510 Ventricular fibrillation HSDN C0020578 Hyperventilate C3553264 Joubert syndrome 17 MalaCards C0522224 Palsied C0015300 Exophthalmos HSDN C4084802 Usual severity diarrhea C0036674 Sensory deprivation HSDN C2700617 Irritation - emotion C1838570 Ceroid lipofuscinosis, neuronal, 8 MalaCards C0042963 Symptoms vomiting C0242658 Homosexuality male HSDN C0041105 Jaw spasm C0038363 Aphthous stomatitis HSDN C0022408 Disorder joint C2939462 Immunoglobulin deposition disease MalaCards C0857305 Thrombocytopenia purpura C0220847 C hepatitis virus HSDN C4084776 Weight loss C0684274 Self regulation HSDN C1963090 Dehydration adverse event C1832386 Diabetes mellitus, transient neonatal, 1 OrphaNet|HPO|MalaCards C4082202 Sleep quality question C0342859 Harderoporphyria HPO C0013604 Edematous C0008924 Cleft lip HSDN C2024893 Cardiovascular surgery result: fatigue C0241158 Cicatrix skin HSDN C0085642 Asphyxia reticularis C0040028 Thrombocythemia, essential HSDN C0030552 Paralysis partial C0751795 Head injury penetrating HSDN C0020580 Decreased sensation C1963178 Myelitis adverse event HSDN C1963184 Nystagmus adverse event C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C0041657 Consciousness loss C0018839 Heat exhaustion HSDN C0033377 Caudal displacement C0021345 Infectious mononucleosis MalaCards C3539020 Pelvic pain decreasing in frequency C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C3641755 Have constipation C0033770 Prune belly syndrome OrphaNet|HPO|MalaCards C0009806 Constipate C0162532 Variegate porphyria MalaCards|HPO|UMLS C1069915 Vertigo C0021655 Insulin resistance HSDN C0018681 Headache, cephalalgia C0032269 Pneumococcal infections HSDN C0019825 Voice hoarseness C1527344 Dysphonia UMLS C0042024 Urine incontinence C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C3641755 Have constipation C0038160 Staphylococcal infections HSDN C4084723 Constipation C0268407 Senile cardiac amyloidosis MalaCards C3541349 Syncope C0037930 Spinal cord neoplasms HSDN C3887638 Failure to thrive in infant C0342871 Acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C0016382 Cutaneous vascular engorgement C1851502 Erythema palmare hereditarium MalaCards C0018784 Deafness sensorineural C2931205 Usher syndrome, type 1a MalaCards C0520588 Vulvovaginal pain C0406670 Burning vulva UMLS C0018772 Deafness C0022865 Obstetric labor complications HSDN C0476273 Distress respiratory C1970270 Choreoathetosis and congenital hypothyroidism HPO C1557397 Adverse event associated with pain C0031048 Pericarditis, constrictive HSDN C0010200 Cough symptom C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN|UMLS C0036572 Convulsion C3897759 Recurrent childhood anaplastic oligodendroglioma UMLS C0002962 Angina C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0011991 Loose stools C0032914 Pre-eclampsia HSDN C0424755 Fever symptoms C0305062 Tetanus toxoids HSDN C3541349 Syncope C2945560 Hemolytic HSDN C0018784 Deafness sensorineural C1623209 Okihiro syndrome MalaCards|HPO C4084776 Weight loss C0020255 Hydrocephalus HSDN C0030193 Sense of pain C0013386 Dyskinesia, drug-induced HSDN C0007758 Cerebellar ataxia C2931872 Free sialic acid storage disease OrphaNet|MalaCards C0000737 Abdomen pain C0700095 Central neuroblastoma MalaCards|HSDN C0018991 Paralysis one side of body C0032227 Pleural effusion disorder HSDN C2203646 Jaundice C0740277 Bile duct carcinoma OrphaNet|HPO C0002170 Alopecia disorders C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C0030552 Paralysis partial C0009240 Cognition HSDN C2187990 Unable to perform sex C0206247 Amyloid neuropathies MalaCards C0742302 Chest pain site anterior chest C0741025 Chest problem UMLS C0312416 Morning sickness C0269661 Emesis pregnancy UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0040046 Thrombophlebitis HSDN C2911647 Weight gain adverse event C0014544 Epilepsy HSDN C1069915 Vertigo C0007020 Carbon monoxide poisoning HSDN C1527344 Dysphonia C1860315 Whispering dysphonia, hereditary MalaCards C0030552 Paralysis partial C0011849 Diabetes mellitus HSDN C0019209 Large liver C1859228 Cerebrohepatorenal syndrome, variant types HPO C2029884 Hearing loss by exam C0559260 Congenital scoliosis HSDN C2096293 Ent surgical result ear vertigo C0342257 Complications of diabetes mellitus HSDN C4084775 Usual severity weight loss C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse MalaCards C0028738 Nystagmus C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C4042891 Sleep wake disorders C0018818 Ventricular septal defects HSDN C3665347 Vision impaired C1832466 Capos syndrome OrphaNet|HPO C0038990 Sweats C0242287 Isaacs syndrome OrphaNet|HPO|MalaCards C0035232 Diaphragmatic paralysis C0006287 Bronchopulmonary dysplasia MalaCards C0019825 Voice hoarseness C0015379 Extravasation of diagnostic and therapeutic materials HSDN C0034933 Abnormal reflexes C0025958 Microcephaly HSDN C0427055 Face weakness C0025286 Meningioma MalaCards C3641756 Have diarrhea C1863239 Partial adenosine deaminase deficiency HPO C2919142 Short stature adverse event C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C0030193 Sense of pain C0033953 Psychosexual disorders HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242659 Female homosexual HSDN C1549543 Administration method - pain C0020458 Hyperhidrosis disorder HSDN C1963093 Dizziness adverse event C1836438 Familial neurocardiogenic syncope MalaCards C4085222 Nausea C0853697 Neutrophil count decreased HSDN C4084776 Weight loss C0242310 Igm heavy chain disease OrphaNet|MalaCards C0424755 Fever symptoms C0524909 Hepatitis b, chronic MalaCards|HSDN C4042891 Sleep wake disorders C0021364 Male infertility HSDN C0423742 Intercourse pain C0006845 Candidiasis, chronic mucocutaneous OrphaNet|HPO|MalaCards C0042025 Urinary incontinence stress C0018916 Hemangioma HSDN C0237326 Defecation pain C0431406 Asymmetric crying face association OrphaNet|HPO C1963091 Diarrhea adverse event C0015656 Fasciolopsiasis DiseaseOntology C4050613 Anxiety C0339534 Usher syndrome type 2 MalaCards|HPO C0003469 Anxiety disorder C3683846 Chromosome 17p deletion syndrome MalaCards C0237326 Defecation pain C1563716 Thyroid dysgenesis HPO C0034933 Abnormal reflexes C0517555 Venous thrombosis after immobility HSDN C0043094 Weight gain C0036421 Systemic scleroderma HSDN C0026821 Cramp C2931395 Bulbospinal neuronopathy, x-linked recessive HPO C2919142 Short stature adverse event C1860471 Stoll alembik dott syndrome MalaCards C0037317 Sleep disturbance C0342443 Adrenal cushing's syndrome MalaCards C0010200 Cough symptom C0009447 Common variable immunodeficiency HSDN C3541349 Syncope C0014117 Endocardial fibroelastosis HSDN C4084767 Bothered by vomiting C0853697 Neutrophil count decreased HSDN C3641755 Have constipation C0017612 Glaucoma, open-angle HSDN C0018784 Deafness sensorineural C0344487 Lateral meningocele MalaCards C2984058 Have pain C2004487 Vaginal spasm HSDN C0019825 Voice hoarseness C1512861 Intermediate differentiated ovarian sertoli-leydig cell tumor, variant with heterologous elements UMLS C2315100 Pediatric failure to thrive C0020626 Hypoparathyroidism HSDN C2919142 Short stature adverse event C0796088 Neurofaciodigitorenal syndrome OrphaNet|MalaCards C0036572 Convulsion C0438419 Unilateral epilepsy UMLS C0024031 Back pain lower back C0020542 Pulmonary hypertension HSDN C0009398 Color vision defects C3178817 Paraneoplastic syndromes, ocular HSDN C0262527 Intermittent abdominal pain C0153653 Malignant tumor of parathyroid gland MalaCards C0003113 Anomia C0014038 Encephalitis HSDN C0005745 Blepharoptosis C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C0030193 Sense of pain C0014378 Enterovirus infections HSDN C1963252 Tremor adverse event C1848211 Mental retardation with psychosis, pyramidal signs, and macroorchidism MalaCards|HPO C0232462 Appetite decrease C0024620 Primary malignant neoplasm of liver MalaCards C0012833 Dizzy C0040028 Thrombocythemia, essential MalaCards C3641755 Have constipation C0007784 Cerebral hemisphere hemorrhage HSDN C3541349 Syncope C0013481 Ebstein anomaly HSDN C3665347 Vision impaired C0027877 Neuronal ceroid-lipofuscinoses OrphaNet|MalaCards C0518090 Frequency of pain question C0024793 Marek disease HSDN C1963252 Tremor adverse event C0026946 Mycoses HSDN C0030193 Sense of pain C0001427 Adenoiditis, nos MalaCards C4084802 Usual severity diarrhea C1865643 Cholestasis, progressive familial intrahepatic 3 HPO C0000737 Abdomen pain C1269683 Major depressive disorder HSDN C0038990 Sweats C1721007 Pachyonychia congenita, type 2 (disorder) MalaCards C0039070 Collapse fleeting C0020625 Hyponatremia UMLS C2911645 Weight loss adverse event C0015579 Family characteristics HSDN C0026821 Cramp C1833508 Carnitine palmitoyltransferase ii deficiency, late-onset HPO|UMLS C0002965 Crescendo angina C0004096 Asthma HSDN C0019572 Hairiness C0035934 Rubinstein-taybi syndrome HPO C2242996 Tingling C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C1557397 Adverse event associated with pain C0019310 Hernia, obturator HSDN C4084776 Weight loss C0018802 Congestive heart failure HSDN C2984058 Have pain C0020217 Hydatidiform mole HSDN C1557397 Adverse event associated with pain C0039585 Androgen-insensitivity syndrome HSDN C0851578 Disorder sleep C0034186 Pyelonephritis HSDN C0018524 Hallucinate C1846707 Spinocerebellar ataxia 17 MalaCards|HPO C0023012 Delay language C3150756 Chromosome 4q21 deletion syndrome MalaCards C1963065 Apnea adverse event C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0024031 Back pain lower back C1565489 Renal insufficiency HSDN C1963137 Hydrocephalus adverse event C1876203 Frontonasal dysplasia MalaCards C2984058 Have pain C1868649 Panic disorder 1 HSDN C1145670 Failure respiratory C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C0042963 Symptoms vomiting C0279659 Adenocarcinoma of the extrahepatic bile duct UMLS C0023014 Developmental disorder language C0023676 Life style HSDN C4084775 Usual severity weight loss C3887662 Intraspinal neoplasm HSDN C0015469 Facial paralysis C0013182 Drug allergy HSDN C0030486 Extremity paralysis, lower C0021359 Infertility HSDN C0003962 Ascites C0221013 Mastocytosis, systemic MalaCards C0747556 Pharyngitis recurrent C0032533 Polymyalgia rheumatica MalaCards C1549543 Administration method - pain C0025517 Metabolic diseases HSDN C3641756 Have diarrhea C0018674 Head trauma HSDN C0349588 Stature short C1876175 Ataxia-telangiectasia variant MalaCards|HPO C0518090 Frequency of pain question C2607914 Allergic rhinitis (disorder) HSDN C0030193 Sense of pain C3873472 Vulvovaginal gingival syndrome MalaCards C0151686 Growth retardation C1859084 Citrulline transport defect MalaCards C0026826 High muscle tone C1860157 Elejalde disease MalaCards C0041667 Low weight C0268140 Xeroderma pigmentosum, group f HPO C3898969 Have been vomiting C0010072 Coronary thrombosis HSDN C0011991 Loose stools C3280314 Combined malonic and methylmalonic aciduria MalaCards C4084725 Usual severity cough C0037933 Spinal diseases HSDN C0036572 Convulsion C0751781 Dentatorubral-pallidoluysian atrophy HPO|UMLS C1963087 Constipation adverse event C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C2203646 Jaundice C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C0018681 Headache, cephalalgia C0033817 Pseudomonas infections HSDN C1963281 Vomiting adverse event C0268569 Intermittent maple syrup urine disease HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0017417 Genital neoplasms, male HSDN C1384666 Decreased hearing C0040128 Thyroid diseases HSDN C0013404 Respiratory difficulty C0014859 Esophageal neoplasms HSDN C2984058 Have pain C1705810 Generic role HSDN C4084727 Cough frequency C3809651 Infantile liver failure syndrome 2 MalaCards C3274924 Have been coughing C0011854 Diabetes mellitus, insulin-dependent HSDN C1565249 Limitation, mobility C0003850 Arteriosclerosis HSDN C4084775 Usual severity weight loss C3827868 Tachycardia by ecg finding HSDN C4084774 Have weight loss C0036421 Systemic scleroderma OrphaNet|HSDN|MalaCards C4084773 Bothered by weight gain C0015726 Focused anxiety HSDN C0085631 Abnormal excitement C0037744 Perceptual spatial orientation HSDN C4085210 Usual severity pain C0032002 Pituitary diseases HSDN C1963091 Diarrhea adverse event C1304456 Congo hemorrhagic fever MalaCards C4085317 Diarrhea frequency C0036357 Psychology, schizophrenic HSDN C0034150 Skin purpura C0041327 Tuberculosis, pulmonary HSDN C0002170 Alopecia disorders C0021071 Immunoproliferative small intestinal disease MalaCards C4085642 Level of joint stiffness C0043207 Wolfram syndrome MalaCards|HPO C0008031 Pain chest C0011854 Diabetes mellitus, insulin-dependent HSDN C0018784 Deafness sensorineural C1261128 Progeria-like syndrome MalaCards C4085548 Usual severity dizziness C2984330 Chagas disease pathway HSDN C0039231 Heartbeats increased C0035022 Tick-borne relapsing fever DiseaseOntology|MalaCards C0031911 Pigment deposition C0238137 Gallbladder adenoma MalaCards C0575081 Abnormal gait C3160718 Parkinson disease, late-onset MalaCards C0033774 Skin pruritus C0020473 Hyperlipidemia HSDN C0151786 Weakness muscle C0037932 Curvature of spine HSDN C0007859 Pain neck C0039144 Syringomyelia HSDN C0151786 Weakness muscle C1845151 Glycogen storage disease, type ixd HPO|UMLS C0917816 Deficiency mental C1858054 Bardet-biedl syndrome 6 MalaCards|HPO C4085222 Nausea C0036974 Shock HSDN C0221166 Paraparesis C1844865 Charcot-marie-tooth disease, x-linked recessive, 3 (disorder) OrphaNet C3665492 Pigmentations C0751396 Well differentiated oligodendroglioma MalaCards C0522224 Palsied C1963084 Colitis adverse event HSDN C0522224 Palsied C0036868 Sex chromosome aberrations HSDN C0043352 Absent salivary secretion C1867059 Parotid aplasia or hypoplasia HPO C0010200 Cough symptom C0029463 Osteosarcoma HSDN C3641756 Have diarrhea C0001727 Afferent loop syndrome HSDN C3463815 Feel fatigue C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C3665347 Vision impaired C3494489 Autoimmune polyendocrinopathy syndrome, type 1 OrphaNet|HPO C0009421 Comatose C0037275 Skin diseases, vesiculobullous HSDN C4084766 Vomiting C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C0035232 Diaphragmatic paralysis C2350350 Ventilator induced lung injury HSDN C0018808 Murmur C0553980 Endomyocardial fibrosis HSDN C4084784 Diarrhea C0018023 Nodular goiter HSDN C2911645 Weight loss adverse event C0033586 Failure, prosthesis HSDN C0015402 Hemorrhage eye C0024535 Malaria, falciparum HSDN C2984058 Have pain C0006437 Burn, inhalation HSDN C0040822 D tremors C0334419 Pheochromocytoma, malignant MalaCards|UMLS C0009676 Confusion state C0014553 Absence epilepsy HSDN C0023015 Language handicap C2984291 Glioblastoma multiforme pathway HSDN C3641756 Have diarrhea C0014055 Encephalitis, epidemic HSDN C0151786 Weakness muscle C1835922 Aminoacylase 1 deficiency MalaCards|HPO|UMLS C4084727 Cough frequency C1761609 Aspiration pneumonitis MalaCards C1963090 Dehydration adverse event C1846220 Adrenal hypoplasia, congenital, with precocious puberty HPO C1263846 Attention deficit disorder with hyperactivity C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C3815497 Cough C0038663 Suicide attempt HSDN C0042024 Urine incontinence C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO C0424755 Fever symptoms C0036868 Sex chromosome aberrations HSDN C0013604 Edematous C0008372 Intrahepatic cholestasis HSDN C1963091 Diarrhea adverse event C0032310 Pneumonia, viral HSDN C0018772 Deafness C0010414 Infection by cryptococcus neoformans HSDN C4085210 Usual severity pain C0035078 Kidney failure HSDN C0013604 Edematous C0003534 Aphakia HSDN C1963086 Confusion adverse event C0751587 Cadasil syndrome OrphaNet|HPO C2024893 Cardiovascular surgery result: fatigue C0029896 Disease, ent HSDN C0037317 Sleep disturbance C0268543 Hyperammonemia, type iii MalaCards C0750394 Wbc low C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C3641756 Have diarrhea C0037397 Behavior social HSDN C0231528 Muscle pain generalized C1535917 Nipah virus infection MalaCards C2919142 Short stature adverse event C1832817 Klippel-feil deformity, conductive deafness, and absent vagina OrphaNet|MalaCards C0018681 Headache, cephalalgia C1541317 Adult gliosarcoma UMLS C0151786 Weakness muscle C4042784 Feeding and eating disorders HSDN C0030552 Paralysis partial C0027947 Neutropenia HSDN C0036572 Convulsion C0005818 Blood platelet disorders HSDN C0015672 Decreased energy C0036690 Septicemia HSDN C4084802 Usual severity diarrhea C0005940 Bone diseases HSDN C0040264 Ear ringing sound C0015467 Neuralgia facial HSDN C0235014 Fontanel bulging C0272199 Familial hemophagocytic lymphocytosis MalaCards|UMLS C4085317 Diarrhea frequency C0282193 Iron overload HSDN C0018784 Deafness sensorineural C2931356 Spastic paraplegia type 5a, recessive MalaCards C0015230 Exanthem C0086196 Eczema, infantile UMLS C0042798 Vision dim C1579931 Depressed - symptom HSDN C1836296 Lower extremity weakness C0745883 Lower extremity polio UMLS C0020672 Body temperature decreased C0342257 Complications of diabetes mellitus HSDN C0027424 Congestion nasal C0700148 Congestion UMLS C4084784 Diarrhea C1855869 Autoimmune polyendocrinopathy syndrome, type i, autosomal dominant HPO C3539896 Pelvic pain occurs with urination C0009404 Colorectal neoplasms HSDN C4084768 Usual severity vomiting C4012395 Congenital disorder of glycosylation, type iy MalaCards C0020450 Hyperemesis gravidarum C0032797 Postpartum hemorrhage HSDN C3829611 Nausea frequency C0002351 Altitude sickness HSDN C4084774 Have weight loss C0003467 Anxiety HSDN C4085317 Diarrhea frequency C0006114 Cerebral edema HSDN C0232466 Feeding difficulty C3665349 Secondary hypothyroidism OrphaNet|MalaCards C0009676 Confusion state C0035302 Retinal artery occlusion HSDN C1527344 Dysphonia C0028064 Niemann-pick diseases MalaCards C3898969 Have been vomiting C0040247 Tinea HSDN C0039070 Collapse fleeting C0014849 Esophageal and gastric varices HSDN C0036659 Sensation disorder C0034065 Pulmonary embolism HSDN C0043094 Weight gain C3280817 Hypothyroidism, congenital, nongoitrous, 6 MalaCards C0557874 Global developmental delay C1837429 Pyruvate dehydrogenase phosphatase deficiency MalaCards|HPO C1963281 Vomiting adverse event C0035457 Rhinitis, allergic, perennial HSDN C0026838 Spasticity muscle C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C4085549 Dizziness C0001818 Agoraphobia HSDN C0030552 Paralysis partial C0005491 Biofeedback HSDN C0497406 Over weight C0040053 Thrombosis HSDN C0349588 Stature short C0265226 Hecht syndrome (disorder) OrphaNet|HPO C2984058 Have pain C0028064 Niemann-pick diseases HSDN C1963063 Anorexia adverse event C2931183 Faces syndrome OrphaNet|MalaCards C0013421 Dystonia C0028768 Obsessive-compulsive disorder HSDN C0002622 Amnesias C0236642 Pick disease of the brain HSDN C1069915 Vertigo C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0684343 Pseudophakia C1536085 Geographic atrophy HSDN C1963093 Dizziness adverse event C0014836 Escherichia coli infections HSDN C0000727 Abdomen acute C0024205 Lymphadenitis HSDN C3539889 Pelvic pain increasing in severity C1961100 Erectile dysfunction adverse event HSDN C0085636 Light sensitivity C1963266 Uveitis adverse event HSDN C0004941 Behavioral symptoms C1848561 Methylmalonic acidemia with homocystinuria OrphaNet|MalaCards C0727671 Red cross toothache drops C0008065 Childhood behavior HSDN C4085317 Diarrhea frequency C0087130 Uncertain HSDN C2185934 Loss of hearing on one side only C0521785 Hearing loss, unilateral UMLS C4085222 Nausea C0017168 Gastroesophageal reflux disease HSDN C0036572 Convulsion C0035078 Kidney failure HSDN|UMLS C0018784 Deafness sensorineural C0010417 Cryptorchidism HSDN C0232493 Epigastric pain C0854795 Resectable hepatic malignant neoplasm MalaCards C0020672 Body temperature decreased C0038187 Starvation HSDN C0015672 Decreased energy C0008728 Churg-strauss syndrome OrphaNet|MalaCards C2984057 Have nausea C0270639 Lateral sinus thrombosis HSDN C0019209 Large liver C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C4084773 Bothered by weight gain C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C0015672 Decreased energy C0032964 Pregnancy complications, hematologic HSDN C3539893 Pelvic pain occurs with intercourse C0042065 Genitourinary neoplasms HSDN C0018784 Deafness sensorineural C1863389 Apert-crouzon disease MalaCards C0030552 Paralysis partial C0270611 Brain damage HSDN C0155502 Vertigo benign positional C0004941 Behavioral symptoms HSDN C1963091 Diarrhea adverse event C0006105 Brain abscess HSDN C0600142 Flash hot C0019693 Hiv infections HSDN C0495662 Benign and innocent cardiac murmurs C0018799 Heart diseases UMLS C0030193 Sense of pain C0740487 Sinus, maxillary, cancer, carcinoma UMLS C0004604 Pain back C0017416 Genital neoplasms, female HSDN C1549543 Administration method - pain C0032897 Prader-willi syndrome HSDN C0036572 Convulsion C3281200 Leukoencephalopathy, brain calcifications, and cysts UMLS C0152116 Torticollis spasmodic C2231100 Focal torsion dystonia UMLS C0155552 Hearing loss mixed C0008928 Cleidocranial dysplasia HSDN C0086437 Joint hypermobility C0795989 Hypospadias-mental retardation syndrome MalaCards C2984058 Have pain C0015414 Eye neoplasms HSDN C1963086 Confusion adverse event C0034885 Rectal neoplasms HSDN C0036572 Convulsion C0268568 Classic maple syrup urine disease HPO C1963071 Back pain adverse event C0025521 Inborn errors of metabolism HSDN C0234132 Pyramidal sign C0015306 Hereditary multiple exostoses HPO C4084774 Have weight loss C1704436 Peripheral arterial diseases HSDN C0011991 Loose stools C0021846 Intestinal polyps HSDN C4084727 Cough frequency C0020541 Hypertension, portal HSDN C0151686 Growth retardation C3553512 Immunodeficiency, common variable, 8, with autoimmunity MalaCards C0004134 Dyssynergia C1847640 Kufor-rakeb syndrome MalaCards C0019079 Bloody sputum C0862793 Adenocarcinoma iiib lung stage UMLS C0015970 Fever unknown origin C1619738 Immune reconstitution inflammatory syndrome HSDN C1963091 Diarrhea adverse event C0242698 Ventricular dysfunction, left HSDN C0010200 Cough symptom C0153416 Malig neop oth spec part oesop MalaCards C1963154 Renal failure adverse event C0010691 Cystinuria MalaCards C3146279 Coma C0042769 Virus diseases HSDN C1963281 Vomiting adverse event C0043515 Zollinger-ellison syndrome HSDN C4085317 Diarrhea frequency C0010674 Cystic fibrosis HSDN C0460137 Push down or depress C0268322 Chester-type porphyria HPO C0013362 Dysarthrias C1848201 Subcortical band heterotopia HPO C0242936 Center pain C0017160 Gastroenteritis HSDN C0018681 Headache, cephalalgia C0027832 Neurofibromatosis 2 HPO|UMLS C3463815 Feel fatigue C0282193 Iron overload OrphaNet C0014724 Burping C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN C0028738 Nystagmus C3554321 Basal ganglia calcification, idiopathic, 4 MalaCards C3539892 Pelvic pain in front C0007860 Uterine cervicitis HSDN C0043068 Friderichsen-waterhouse syndrome C1963211 Pericarditis adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2188545 Anuria HSDN C1549543 Administration method - pain C0023801 Lipomatosis HSDN C4084802 Usual severity diarrhea C0006057 Botulisms MalaCards C0018681 Headache, cephalalgia C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C0542476 Forgetful C0011644 Scleroderma MalaCards C0349588 Stature short C2931420 Brachydactylous dwarfism mseleni type OrphaNet|MalaCards C0454644 Delayed language development C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C0042940 Disorder of voice C0021400 Influenza HSDN C0812426 Kidney problem C0003836 Nephrosclerosis arterial UMLS C0282005 Scrotum swelling C0741437 Male_repro problem UMLS C3829611 Nausea frequency C0015802 Femur fracture HSDN C0030193 Sense of pain C0025490 Mesonephroma HSDN C0030552 Paralysis partial C0460137 Push down or depress HSDN C1962972 Proteinuria adverse event C0034067 Pulmonary emphysema HSDN C1963071 Back pain adverse event C0393735 Headache disorders HSDN C0497247 Blood pressure elevation C1719313 Hereditary amyloid nephropathy MalaCards C0151786 Weakness muscle C0220998 Hypothalamic hypothyroidism MalaCards C0270948 Neurogenic muscular atrophy C3888317 Sialidosis, type 2 OrphaNet C0233794 Memory impaired C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C4084724 Usual severity constipation C0040053 Thrombosis HSDN C1971624 Appetite absent C0436596 On examination - apathetic HSDN C0851578 Disorder sleep C0027439 Nasopharyngeal neoplasms HSDN C0020305 Fetal edema C1855652 Fetus small for gestational age HSDN C0460137 Push down or depress C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C0020672 Body temperature decreased C0019195 Hepatitis, viral, human HSDN C0231528 Muscle pain generalized C4048826 Mud fever MalaCards C0086437 Joint hypermobility C0268337 Ehlers-danlos syndrome, type 3 (disorder) HPO C0030193 Sense of pain C0206704 Carcinoma, large cell HSDN C4085661 Usual severity nausea C0232488 Abdominal colic HSDN C0026821 Cramp C0020542 Pulmonary hypertension HSDN C0557874 Global developmental delay C1846790 Joubert syndrome 4 (disorder) MalaCards C1856661 Cornea cloudy C0039292 Tangier disease MalaCards|HPO C2984058 Have pain C0009062 Clostridia infection HSDN C4085210 Usual severity pain C0003614 Appendiceal neoplasms HSDN C0522224 Palsied C0008149 Chlamydia infections HSDN C0270790 Quadriparesis C0751072 Frontotemporal lobar degeneration MalaCards C0085593 Chill C1336435 Stage iv mesothelioma of pleura UMLS C0040460 Dental pain C0017601 Glaucomas HSDN C1963184 Nystagmus adverse event C0344467 Biemond syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0014859 Esophageal neoplasms HSDN C0030193 Sense of pain C0033839 Pseudorabies HSDN C0155552 Hearing loss mixed C3814530 Skin vesicle HSDN C0030193 Sense of pain C1328252 Mucocutaneous leishmaniasis HSDN C0751093 Dystonia, limb C0038868 Progressive supranuclear palsy HPO C1962956 Flatulence adverse event C0005750 Blind loop syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0018188 Granuloma HSDN C0349588 Stature short C0265354 Charge syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0040809 Patient refusal of treatment HSDN C0018772 Deafness C0162526 Aids-related opportunistic infections HSDN C4084769 Vomiting frequency C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0022346 Yellow skin C0346647 Malignant neoplasm of pancreas MalaCards|UMLS C0851578 Disorder sleep C0005940 Bone diseases HSDN C1963071 Back pain adverse event C0038160 Staphylococcal infections HSDN C0022346 Yellow skin C1384665 Hfe gene HSDN C0518090 Frequency of pain question C0015423 Eyelid diseases HSDN C1549543 Administration method - pain C0025295 Meningitis, pneumococcal HSDN C0012833 Dizzy C0271493 Angiospastic ophthalmo-auricular syndrome UMLS C4085211 Pain distress question C0080274 Urinary retention HSDN C0027497 Queasy C0004692 Balantidiasis MalaCards C0221232 Welts C1304181 Allergic urticaria due to inhaled agent UMLS C2315100 Pediatric failure to thrive C1845408 Contiguous abcd1-dxs1375e deletion syndrome MalaCards|HPO C4085549 Dizziness C0008370 Cholestasis HSDN C0033377 Caudal displacement C1266101 Thymic epithelial tumor OrphaNet C1963086 Confusion adverse event C0027773 Nesidioblastosis HSDN C0020305 Fetal edema C0039232 Supraventricular tachycardia av node reentrant HSDN C1963063 Anorexia adverse event C0026769 Multiple sclerosis HSDN C0043094 Weight gain C0040128 Thyroid diseases HSDN C4084724 Usual severity constipation C0042138 Uterine neoplasms HSDN C0019572 Hairiness C0022735 Klinefelter syndrome HSDN C4084774 Have weight loss C0085073 Prosthesis-related infection HSDN C0018681 Headache, cephalalgia C0011649 Dermoid cyst HSDN C1279888 Proteinuria of undiagnosed cause C0017205 Gaucher disease MalaCards C0013395 Indigestion C0010674 Cystic fibrosis HSDN C2984057 Have nausea C0019348 Herpes simplex infections HSDN C0020455 Hypergammaglobulinemia C1800706 Idiopathic pulmonary fibrosis MalaCards|HPO C0015402 Hemorrhage eye C0041296 Tuberculosis HSDN C2984058 Have pain C0007527 Cecal disease HSDN C0518090 Frequency of pain question C0009062 Clostridia infection HSDN C0012833 Dizzy C1719788 Episodic ataxia type 1 HPO|UMLS C0004604 Pain back C0024636 Malocclusion HSDN C0151686 Growth retardation C0268251 Gaucher disease, type 3 (disorder) OrphaNet C2029884 Hearing loss by exam C0001828 Agricultural workers' diseases HSDN C0019214 Hepatosplenomegaly C0023518 Leukocytosis MalaCards C0042963 Symptoms vomiting C1691228 Cystic kidney diseases HSDN C0476273 Distress respiratory C1856403 Etfb deficiencies HPO C0042963 Symptoms vomiting C0011849 Diabetes mellitus HSDN C2242996 Tingling C0085677 Alcoholic neuropathy HSDN C0002963 Angina variant C0026654 Moyamoya disease HSDN C4084725 Usual severity cough C0025202 Melanoma HSDN C0028738 Nystagmus C2745997 Orofaciodigital syndrome vi MalaCards|HPO C0497406 Over weight C3813607 Infantile gastroesophageal reflux HSDN C4085862 Bothered by nausea C0009021 Clonorchiasis DiseaseOntology C4085222 Nausea C0027873 Neuromyelitis optica MalaCards|HSDN C0030193 Sense of pain C0041333 Tuberculosis genitourinary HSDN C3274924 Have been coughing C1963067 Atrial fibrillation adverse event HSDN C0000737 Abdomen pain C3888013 Hypnoses HSDN C0086437 Joint hypermobility C0268341 Ehlers-danlos syndrome type 5 MalaCards C4084723 Constipation C2981150 Uranostaphyloschisis HSDN C0042571 Vertigo subjective C0008350 Cholelithiasis HSDN C0030975 Disorders perception C0302826 Expressed emotion HSDN C0239451 Eyelid burning sensation C1112366 Eyelid irritation UMLS C0018784 Deafness sensorineural C2936830 Chromosome 13 duplication OrphaNet|MalaCards C0009806 Constipate C0080174 Spina bifida occulta HSDN C0750016 Urticaria generalized C0042109 Urticaria UMLS C0026821 Cramp C0004775 Bartter disease HSDN C0002965 Crescendo angina C0033923 Psychomotor function HSDN C0019079 Bloody sputum C2239176 Liver carcinoma HSDN C0020455 Hypergammaglobulinemia C1565489 Renal insufficiency HSDN C2096293 Ent surgical result ear vertigo C1136041 Familial acoustic neuroma OrphaNet|HPO C2237041 Shox gene with short stature C2931294 Wiedemann grosse dibbern syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0005716 Blastomycosis HSDN C0242936 Center pain C0149925 Small cell carcinoma of lung HSDN C0022346 Yellow skin C1423541 Vangl2 gene HSDN C2029884 Hearing loss by exam C0024694 Mandibular neoplasms HSDN C0013404 Respiratory difficulty C0546817 Fluid overload UMLS C3539891 Pelvic pain to the rear C0022665 Kidney neoplasm HSDN C0392156 Acathesia C0162550 Akathisia, drug-induced UMLS C0034933 Abnormal reflexes C0234421 Conscious HSDN C0004604 Pain back C0039128 Syphilis HSDN C0011991 Loose stools C0006114 Cerebral edema HSDN C0030232 Color loss C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0838226 Pain in a joint, pelvic region and thigh C0810055 Other non-traumatic joint disorders UMLS C1963071 Back pain adverse event C0003504 Aortic valve insufficiency HSDN C2984058 Have pain C0006107 Concussion HSDN C0020455 Hypergammaglobulinemia C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C1963252 Tremor adverse event C0268226 Type i mucolipidosis OrphaNet|HPO C1963154 Renal failure adverse event C0403557 Glomerulopathy with giant fibrillar deposits MalaCards C0036572 Convulsion C2675897 1q21.1 contiguous gene deletion MalaCards C0036572 Convulsion C0020255 Hydrocephalus HSDN|HPO C0004604 Pain back C2931645 Ochronosis, hereditary MalaCards C1962972 Proteinuria adverse event C0027947 Neutropenia HSDN C2919142 Short stature adverse event C1866688 Spondylometaphyseal dysplasia, algerian type OrphaNet|HPO|MalaCards C0233514 Behavior abnormal C0751208 Juvenile huntington disease MalaCards C0002962 Angina C3542413 Cdisc adas-cog - comprehension HSDN C1850830 Exercise-induced muscle pain C0410207 Tubular aggregate myopathy MalaCards|HPO C4084774 Have weight loss C0162534 Prion diseases HSDN C4084776 Weight loss C0003950 Ascariasis HSDN C0012569 Double vision C1847839 Episodic ataxia, type 3 MalaCards C4084776 Weight loss C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C4084788 Have dizziness C0007856 Cervical rib syndrome HSDN C0231218 Malaise generalized C0520779 Human ehrlichial infection, sennetsu type MalaCards C0476273 Distress respiratory C1850106 Raine syndrome MalaCards C0040034 Thrombocytopenia C2718078 Deficiency of uroporphyrinogen iii synthase MalaCards|HPO C4085211 Pain distress question C0009062 Clostridia infection HSDN C4020887 Photodysphoria C0032001 Pituitary apoplexy MalaCards C0009806 Constipate C0021603 Sleep initiation and maintenance disorders HSDN C3641756 Have diarrhea C0033860 Psoriasis HSDN C3898969 Have been vomiting C0037005 Shoulder dislocation HSDN C4084775 Usual severity weight loss C0014356 Enterocolitis HSDN C0018834 Brash C0432364 Accutane dysmorphic syndrome MalaCards C4084769 Vomiting frequency C0013595 Eczema HSDN C0151740 Intracranial hypertension C0033845 Pseudotumor cerebri MalaCards C0030193 Sense of pain C0678236 Rare diseases HSDN C0040485 Wryneck C1851945 Dystonia 1, torsion, autosomal dominant HPO|UMLS C4084776 Weight loss C0026896 Myasthenia gravis HSDN C0009676 Confusion state C0035143 Repression HSDN C1000483 Genus anemia C0206636 Chondromatosis MalaCards C1549543 Administration method - pain C0013264 Muscular dystrophy, duchenne HSDN C0700078 Deep tendon reflex decrease C2932716 Pseudohypoparathyroidism type 1c HPO C1882272 Pain adverse event by ctcae anatomic descriptor C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C0007758 Cerebellar ataxia C0006267 Bronchiectasis HSDN C1963281 Vomiting adverse event C2675211 Episodic ataxia, type 6 (disorder) MalaCards C0030554 Abnormal sensation C1997249 Neuralgia, pudendal MalaCards C0018965 Blood urine C0002895 Anemia, sickle cell MalaCards|HPO C0030193 Sense of pain C0677866 Brain stem neoplasms HSDN C0857305 Thrombocytopenia purpura C0019196 Hepatitis c HSDN C0036572 Convulsion C1859974 Glucocorticoid deficiency 1 HPO|UMLS C1963091 Diarrhea adverse event C0030319 Panic disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1868649 Panic disorder 1 HSDN C0002962 Angina C0005395 Bile duct diseases HSDN C4084775 Usual severity weight loss C0016663 Pathological fracture HSDN C0008031 Pain chest C1334670 Mediastinal mixed embryonal carcinoma and teratoma UMLS C0036572 Convulsion C1568272 Tendinopathy HSDN C0034933 Abnormal reflexes C0009450 Disease caused by microorganism HSDN C4084769 Vomiting frequency C0007125 Carcinoma, ehrlich tumor HSDN C4084766 Vomiting C0018571 Hand injury HSDN C4084776 Weight loss C0021051 Immunologic deficiency syndromes HSDN C1549543 Administration method - pain C0040137 Thyroid nodule HSDN C4084723 Constipation C0001175 Acquired immunodeficiency syndrome HSDN C0020505 Excessive eating C3146297 Study of behavior during childhood HSDN C1971624 Appetite absent C1963064 Anxiety adverse event HSDN C0002962 Angina C0007570 Celiac disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0750426 Wbc elevated HSDN C0011991 Loose stools C0042018 Urinary calculi HSDN C1384666 Decreased hearing C0265374 Warfarin syndrome MalaCards C1963093 Dizziness adverse event C0002989 Epithelioid hemangioma of skin HSDN C2984058 Have pain C0221018 Hereditary sideroblastic anemia HSDN C0036572 Convulsion C0023220 Leg injury HSDN C0312422 Blackout spell C0340854 Situational syncope UMLS C2024878 Cardiovascular surgery result: dyspnea C1540912 Hypereosinophilic syndrome HSDN C0019825 Voice hoarseness C0011168 Deglutition disorders UMLS C4084767 Bothered by vomiting C0004161 Athletic injuries HSDN C2984058 Have pain C0162637 Strongylida infections HSDN C1557397 Adverse event associated with pain C0038833 Superior vena cava syndrome HSDN C4084788 Have dizziness C0014474 Ependymoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0039590 Testicular neoplasms HSDN C0013421 Dystonia C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0587047 Mass of trunk C0030283 Pancreatic cyst UMLS C0015672 Decreased energy C0854891 Malignant pleural mesothelioma recurrent UMLS C2242996 Tingling C0011119 Decompression sickness HSDN C1963281 Vomiting adverse event C0023267 Fibroid tumor HSDN C0271215 Blindness legal C0220701 Retinitis pigmentosa 1 MalaCards C0015300 Ocular proptosis C0432263 Craniofacial dysostosis with diaphyseal hyperplasia OrphaNet|MalaCards C1962972 Proteinuria adverse event C0042769 Virus diseases HSDN C0018775 Hearing loss bilateral C0007682 Cns disorder HSDN C1963249 Tinnitus adverse event C1263846 Attention deficit hyperactivity disorder HSDN C1963091 Diarrhea adverse event C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C4084727 Cough frequency C0043324 Juvenile xanthogranuloma HSDN C0231218 Malaise generalized C0267797 Acute hepatitis UMLS C0232466 Feeding difficulty C1865361 Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities HPO C0878773 Bladder hyperactive C0032962 Pregnancy complications HSDN C0151786 Weakness muscle C0151620 Hypertensive encephalopathy HSDN C4084767 Bothered by vomiting C1704326 Role - roleclass HSDN C2024893 Cardiovascular surgery result: fatigue C0006114 Cerebral edema HSDN C0221752 Rbc urine C1274795 Urban schosser spohn syndrome MalaCards C0018777 Deafness, conductive C0037369 Smoking HSDN C3539023 Pelvic pain increasing in frequency C0037051 Behavior illness HSDN C0424755 Fever symptoms C0006663 Calcinosis HSDN C0162834 Hyperpigmentation C0268374 Adult junctional epidermolysis bullosa (disorder) OrphaNet|MalaCards C0018784 Deafness sensorineural C1864276 Deafness, autosomal recessive 17 (disorder) MalaCards C4084773 Bothered by weight gain C0600519 Ventricular remodeling HSDN C0007814 Cerebrospinal fluid otorrhea C0085392 Bacteroidaceae infection HSDN C0151889 Reflexes tendon increased C0796003 Juberg-marsidi syndrome HPO C4085211 Pain distress question C0007760 Cerebellar diseases HSDN C0018784 Deafness sensorineural C1548578 Location characteristic id - smoking HSDN C4042891 Sleep wake disorders C0033677 Protein-energy malnutrition HSDN C0028738 Nystagmus C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C0700590 Diaphoresis excessive C2678439 Cranioosteoarthropathy HPO C0042571 Vertigo subjective C0038661 Suicide HSDN C0010520 Skin cyanosis C0796561 Melanoma vaccines HSDN C0150055 Pain chronic C2984299 Asthma pathway HSDN C4085642 Level of joint stiffness C0265264 Holt-oram syndrome MalaCards C0015672 Decreased energy C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0018681 Headache, cephalalgia C2930971 Acroosteolysis dominant type MalaCards|HPO C0030554 Abnormal sensation C2239112 Blister dosing unit HSDN C4084773 Bothered by weight gain C0000768 Congenital abnormality HSDN C0038002 Spleen enlargement C0272005 Hemoglobin bart's hydrops syndrome MalaCards C1997249 Neuralgia, pudendal C0033578 Prostatic neoplasms HSDN C0036572 Convulsion C2931579 Battaglia neri syndrome OrphaNet|MalaCards C0027796 Neuralgias C0007137 Squamous cell carcinoma HSDN C0026821 Cramp C0027145 Myxedema MalaCards C0005745 Blepharoptosis C0475813 Alpha thalassemia-mental retardation syndrome MalaCards C0233407 Disorient C0349464 Wernicke-korsakoff syndrome MalaCards C4085211 Pain distress question C0392622 Toxic effect of carbon tetrachloride HSDN C0016199 Pain flank C4049328 Kidney medullary carcinoma UMLS C0040034 Thrombocytopenia C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO C1963087 Constipation adverse event C0022660 Kidney failure, acute HSDN C0917816 Deficiency mental C1313961 Trichorrhexis nodosa syndrome MalaCards C0007859 Pain neck C0453996 Tobacco smoking HSDN C0023380 Lethargy C0398597 Histiocytic syndrome HSDN C0086437 Joint hypermobility C0268351 Cutis laxa, autosomal recessive, type i HPO|UMLS C0424755 Fever symptoms C0041318 Tuberculosis, meningeal HSDN C0030794 Pelvis pain C0007621 Neoplastic cell transformation HSDN C0240735 Personality change C0031212 Personality disorders UMLS C4085211 Pain distress question C0751396 Well differentiated oligodendroglioma HSDN C0000737 Abdomen pain C3897537 Stage iia rectal cancer UMLS C0026821 Cramp C0007781 Intracranial embolism and thrombosis HSDN C4084802 Usual severity diarrhea C1857276 Trichohepatoenteric syndrome MalaCards|HPO C0221263 Cafe au lait spot C0037277 Skin diseases, genetic HSDN C4085317 Diarrhea frequency C0013990 Pathological accumulation of air in tissues HSDN C1963281 Vomiting adverse event C1856405 Glutaric aciduria iic HPO C4085211 Pain distress question C0155862 Streptococcal pneumonia HSDN C0086437 Joint hypermobility C3151781 Ck syndrome MalaCards|HPO C0011991 Loose stools C0014805 Primary erythermalgia MalaCards|HPO|UMLS C0042025 Urinary incontinence stress C0019294 Hernia, inguinal HSDN C0521765 Nystagmus unchanged when fixation removed C0028738 Nystagmus UMLS C1963167 Memory impairment adverse event C0220669 Familial benign neonatal epilepsy MalaCards|HPO C4084767 Bothered by vomiting C2240378 Cleft palate on exam HSDN C1963091 Diarrhea adverse event C1868649 Panic disorder 1 HSDN C2032395 Pelvic pain on the left C0001580 Adolescent behavior HSDN C0349588 Stature short C0334123 Histiocytosis, lipoid MalaCards C3665492 Pigmentations C0028326 Noonan syndrome MalaCards C0264611 Apraxia of speech C0282512 Landau-kleffner syndrome MalaCards|HPO C0011991 Loose stools C0473127 Infectious diarrhea prototheca UMLS C0007815 Cerebrospinal fluid rhinorrhoea C0003803 Arnold chiari malformation HSDN C4085210 Usual severity pain C0018671 Head and neck neoplasms HSDN C4084775 Usual severity weight loss C0040558 Toxoplasmosis HSDN C0242936 Center pain C0023348 Leprosy, lepromatous HSDN C4085317 Diarrhea frequency C0037579 Soft tissue neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0345904 Malignant neoplasm of liver MalaCards C0476250 Head neck mass C0264231 Polyp of accessory sinus, nos UMLS C0851578 Disorder sleep C0026948 Mycosis fungoides HSDN C2984058 Have pain C0030297 Pancreatic neoplasm HSDN C0000737 Abdomen pain C0241802 Arthritis, venereal MalaCards C4084726 Distress cough C1532560 Plasmacytoma - category HSDN C1971624 Appetite absent C0027643 Neoplasm recurrence, local HSDN C0024032 Birth weight subnormal C0265223 Cohen syndrome HPO C0039070 Collapse fleeting C0038833 Superior vena cava syndrome HSDN C0036396 Sciatica C0270629 Epidural abscess HSDN C1549543 Administration method - pain C1368355 Synostosis malformation HSDN C1963170 Hypothermia adverse event C0038356 Stomach neoplasms HSDN C0000737 Abdomen pain C0278714 Wilm's tumor, metastatic UMLS C1557397 Adverse event associated with pain C0220981 Metabolic acidosis HSDN C0018777 Deafness, conductive C0175699 Saethre-chotzen syndrome MalaCards|HPO C2073625 X-ray of chest: pleural effusion C1868653 Pancreatitis, calcific HPO C0027796 Neuralgias C0007222 Cardiovascular diseases HSDN C0020438 Hypercalciuria C0004903 Beckwith-wiedemann syndrome MalaCards|HSDN C4084769 Vomiting frequency C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C1384666 Decreased hearing C0497327 Dementia HSDN C1963249 Tinnitus adverse event C2984572 Malaria pathway HSDN C4085862 Bothered by nausea C0001624 Adrenal gland neoplasms HSDN C0241137 Skin pallor C0035204 Respiration disorders HSDN C0035232 Diaphragmatic paralysis C3714580 Hypokalemic periodic paralysis type 1 MalaCards C3829611 Nausea frequency C0001418 Adenocarcinoma HSDN C0917816 Deficiency mental C3275408 Mental retardation, x-linked 96 MalaCards C2984058 Have pain C0520720 Cyst nerve root HSDN C0242936 Center pain C0043168 Whooping cough due to unspecified organism HSDN C0424755 Fever symptoms C0019154 Hepatic vein thrombosis OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C0003850 Arteriosclerosis HSDN C0314719 Dry eyes C0022575 Keratoconjunctivitis sicca UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C1963119 Stomach ulcer adverse event HSDN C1963137 Hydrocephalus adverse event C3489725 Pseudo-torch syndrome MalaCards C0030552 Paralysis partial C0025281 Meniere disease HSDN C0022346 Yellow skin C0861727 Metastatic pancreatic adenocarcinoma UMLS C4085210 Usual severity pain C0006849 Oral candidiasis HSDN C0518090 Frequency of pain question C0014571 Epiphyses, slipped HSDN C4084766 Vomiting C0079774 Peripheral t-cell lymphoma HSDN C3539892 Pelvic pain in front C0042996 Vulvitis unspecified HSDN C3463815 Feel fatigue C0043097 Perception, weight HSDN C3539023 Pelvic pain increasing in frequency C0035358 Retroperitoneal neoplasm HSDN C3815497 Cough C1955864 Cardiac sinus arrest HSDN C0851578 Disorder sleep C0005695 Bladder neoplasm HSDN C4082202 Sleep quality question C0027404 Narcolepsy MalaCards C1971624 Appetite absent C0043251 Wounds and injuries HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0037228 Size perception HSDN C0023015 Language handicap C0038454 Cerebrovascular accident HSDN C4084774 Have weight loss C0014858 Esophageal motility disorders HSDN C0010200 Cough symptom C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C3641756 Have diarrhea C0699744 Infection of ear HSDN C0018681 Headache, cephalalgia C0004114 Astrocytoma HSDN C0026838 Spasticity muscle C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C0005745 Blepharoptosis C0015923 Fetal alcohol syndrome OrphaNet|MalaCards C2919142 Short stature adverse event C3281084 Congenital disorder of glycosylation, type ir MalaCards C0751837 Gait ataxic C0796142 Sao paulo mca-mr syndrome MalaCards|UMLS C0277959 Hair coarseness C1096660 Ehlers-danlos syndrome type ix MalaCards C0151786 Weakness muscle C1510479 Neuralgic amyotrophy OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0039747 Thecoma HSDN C3887638 Failure to thrive in infant C0015624 Fanconi syndrome HSDN|HPO C0030552 Paralysis partial C4024961 Metachromatic leukodystrophy variant MalaCards C4085222 Nausea C0152164 Cyclical vomiting syndrome (disorder) MalaCards C0004134 Dyssynergia C0040136 Thyroid neoplasm HSDN C0518090 Frequency of pain question C0085648 Synovial cyst HSDN C0085632 Listlessness C1838313 Pick complex HPO C0011570 Monopolar depression C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C0424755 Fever symptoms C0149721 Left ventricular hypertrophy HSDN C2024878 Cardiovascular surgery result: dyspnea C0011633 Dermatomyositis HSDN C0026603 Motion sickness C0007760 Cerebellar diseases HSDN C0000737 Abdomen pain C0027794 Neural tube defects HSDN C2984058 Have pain C0003962 Ascites HSDN C2315100 Pediatric failure to thrive C0037268 Skin abnormalities HSDN C4084768 Usual severity vomiting C0268595 Glutaric aciduria, type 1 OrphaNet|HPO C1279888 Proteinuria of undiagnosed cause C0022876 Premature obstetric labor HSDN C3898969 Have been vomiting C0006840 Candidiasis HSDN C3539023 Pelvic pain increasing in frequency C0085222 Psoas muscle abscess HSDN C4042861 Benign obesity, metabolically C0403447 Chronic kidney insufficiency HSDN C0026821 Cramp C1999266 Depression adverse event HSDN C4042891 Sleep wake disorders C0021400 Influenza HSDN C0041657 Consciousness loss C0038356 Stomach neoplasms HSDN C0231528 Muscle pain generalized C0406670 Burning vulva HSDN C3641756 Have diarrhea C0950123 Inborn genetic disease HSDN C2315100 Pediatric failure to thrive C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C0000737 Abdomen pain C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C1557397 Adverse event associated with pain C0041326 Pleural tuberculosis HSDN C4084775 Usual severity weight loss C0041374 Tumor virus infections HSDN C0015672 Decreased energy C0268251 Gaucher disease, type 3 (disorder) OrphaNet|HPO|MalaCards C0152200 Achromatism C0002875 Cooley's anemia HPO C0031315 Phantom limb pain C0039101 Synovial sarcoma HSDN C0242936 Center pain C0025292 Haemophilus meningitis HSDN C0003862 Pain joint C1444838 Chronic arthritis of juvenile onset OrphaNet C4085211 Pain distress question C0011981 Diaphragmatic eventration HSDN C0003862 Pain joint C1623452 Barmah forest virus infection MalaCards C1963065 Apnea adverse event C2706915 Language:-:point in time:^patient:- HSDN C1963071 Back pain adverse event C0033860 Psoriasis HSDN C2203646 Jaundice C0035242 Respiratory tract diseases HSDN C0332563 Papulae C0221011 Malignant atrophic papulosis MalaCards C0262527 Intermittent abdominal pain C0017075 Ganglioneuroma MalaCards C1959630 Eye pain adverse event C0271051 Macular retinal edema HSDN C0162429 Dietary deficiency C2673611 Epidermolysis bullosa dystrophica, autosomal recessive, localisata variant HPO C0518090 Frequency of pain question C0026771 Trauma multiple HSDN C3539889 Pelvic pain increasing in severity C1881674 Medical device emits smoke HSDN C0011168 Disorder deglutition C3463992 Epileptic encephalopathy, early infantile, 1 MalaCards C2984058 Have pain C0154778 Myopia, degenerative HSDN C0018772 Deafness C0034194 Pyloric stenosis HSDN C1963067 Atrial fibrillation adverse event C1449563 Cardiomyopathy, familial idiopathic MalaCards|HPO C0020580 Decreased sensation C0751815 Carotid artery, internal, dissection HSDN C0036396 Sciatica C0853941 Sciatica aggravated UMLS C1963087 Constipation adverse event C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C3463815 Feel fatigue C0017563 Gingival diseases HSDN C1549543 Administration method - pain C0027583 Nematode infections HSDN C0232513 Premature tooth loss C2930971 Acroosteolysis dominant type MalaCards C1557397 Adverse event associated with pain C0013240 Alveolar osteitis HSDN C4085211 Pain distress question C0812470 Abortion, incomplete HSDN C0007758 Cerebellar ataxia C0161409 Cochlear nerve damage HSDN C0020673 Hypothermia (central) (local) C0027809 Neurilemmoma HSDN C4084723 Constipation C0020875 Ileal diseases HSDN C0033774 Skin pruritus C3273135 Extrahepatic bile duct papillary neoplasm with an associated invasive carcinoma UMLS C0010200 Cough symptom C0013806 Electroplexy shock therapy HSDN C4085549 Dizziness C0037929 Spinal cord injuries HSDN C0221232 Welts C1274539 Urticaria due to strongyloidiasis UMLS C0427055 Face weakness C1834671 Facioscapulohumeral muscular dystrophy 1b HPO C2984058 Have pain C0037228 Size perception HSDN C0013395 Indigestion C0018801 Heart failure HSDN C1963137 Hydrocephalus adverse event C0342436 Diencephalic syndrome OrphaNet|MalaCards C0242936 Center pain C0009319 Colitis HSDN C3898969 Have been vomiting C0920350 Autoimmune thyroiditis HSDN C4084784 Diarrhea C1956258 Familial thrombotic thrombocytopenic purpura MalaCards C0037317 Sleep disturbance C0010481 Cushing syndrome MalaCards|HPO C0242670 Chronic vegetative state C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0042571 Vertigo subjective C0002878 Anemia, hemolytic HSDN C1963170 Hypothermia adverse event C0002895 Anemia, sickle cell HSDN C0030975 Disorders perception C0039590 Testicular neoplasms HSDN C4085211 Pain distress question C0085648 Synovial cyst HSDN C0234146 Absent reflex C3809272 Lethal congenital contracture syndrome 5 MalaCards C1963281 Vomiting adverse event C0032851 Disease poultry HSDN C3274924 Have been coughing C0014850 Esophageal atresia HSDN C0518090 Frequency of pain question C0233315 Premature birth of newborn HSDN C0030193 Sense of pain C0041311 Tuberculosis, female genital HSDN C3898969 Have been vomiting C1963068 Atrial flutter adverse event HSDN C1519353 Skin eruption papular C0024137 Lupus erythematosus, cutaneous OrphaNet C2984058 Have pain C0033680 Protein-losing enteropathies HSDN C0008031 Pain chest C1336082 Thymic squamous cell carcinoma UMLS C4084766 Vomiting C0854421 Hanta viral infections MalaCards C0424755 Fever symptoms C1269683 Major depressive disorder HSDN C0151786 Weakness muscle C0011570 Mental depression HSDN C0004604 Pain back C1306759 Eosinophilic disorder HSDN C0009421 Comatose C0268193 Nadh cytochrome b5 reductase deficiency HPO C0018772 Deafness C0005695 Bladder neoplasm HSDN C2911645 Weight loss adverse event C0009862 Contraception behavior HSDN C4084724 Usual severity constipation C0022876 Premature obstetric labor HSDN C4085661 Usual severity nausea C0021933 Intussusception HSDN C1263846 Attention deficit disorder with hyperactivity C0175701 Aarskog syndrome MalaCards|HPO C0013404 Respiratory difficulty C0029443 Osteomyelitis HSDN C4084766 Vomiting C1845892 Hprt deficiency, neurologic variant HPO C0020672 Body temperature decreased C0018674 Head trauma HSDN C3463815 Feel fatigue C0043195 Subsepsis hyperergia syndrome OrphaNet|MalaCards C0018991 Paralysis one side of body C0034040 Puerperal disorders HSDN C0002962 Angina C0037361 Olfactory sense HSDN C0028961 Urine output decreased C3812171 Bradycardia by ecg finding HSDN C0016382 Cutaneous vascular engorgement C0043195 Subsepsis hyperergia syndrome OrphaNet|MalaCards C0015230 Exanthem C2363979 Palmoplantar rash UMLS C0086439 Activity decreased C0376634 Craniofacial abnormalities HSDN C0004604 Pain back C0282333 Relaxation therapies HSDN C3829611 Nausea frequency C0948039 Bacterial gastritis MalaCards C1963063 Anorexia adverse event C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C0027497 Queasy C0025281 Meniere disease HSDN|UMLS C3541349 Syncope C0019195 Hepatitis, viral, human HSDN C0151205 Periorbital edema C0406645 Amyopathic dermatomyositis MalaCards C0028738 Nystagmus C0238286 Mucolipidosis type iv OrphaNet|HPO|MalaCards C0036659 Sensation disorder C0026598 Movement perception HSDN C3887638 Failure to thrive in infant C1836824 Amish infantile epilepsy syndrome HPO C0020580 Decreased sensation C2937358 Cerebral hemorrhage HSDN C0002170 Alopecia disorders C0265329 Organoid nevus phakomatosis OrphaNet|HPO C0542476 Forgetful C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C4085549 Dizziness C0020619 Hypogonadism HSDN C0030552 Paralysis partial C1856302 Gsd iv, nonprogressive hepatic HPO C1963184 Nystagmus adverse event C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C0027796 Neuralgias C0018944 Hematoma HSDN C0012833 Dizzy C0014511 Epithelial cyst HSDN C0020305 Fetal edema C0011981 Diaphragmatic eventration HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206711 Pilomatrixoma HSDN C0018772 Deafness C1963139 Hypopigmentation adverse event HSDN C0231528 Muscle pain generalized C0035410 Rhabdomyolysis UMLS C0151786 Weakness muscle C1853271 Hypophosphatemic rickets with hypercalciuria, hereditary OrphaNet|HPO|UMLS C0036572 Convulsion C0265339 Borjeson-forssman-lehmann syndrome MalaCards|HPO|UMLS C4084768 Usual severity vomiting C0008350 Cholelithiasis HSDN C0878773 Bladder hyperactive C2984299 Asthma pathway HSDN C4084766 Vomiting C0032914 Pre-eclampsia HSDN C0497247 Blood pressure elevation C2930798 Alexanders leukodystrophy MalaCards C0030554 Abnormal sensation C0006436 Burning electric HSDN C2984057 Have nausea C0002986 Fabry disease MalaCards|HPO C0234146 Absent reflex C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C0262384 Chest pain atypical C0002871 Anemia UMLS C2315100 Pediatric failure to thrive C1835845 Mitochondrial phosphate carrier deficiency OrphaNet|HPO|MalaCards C0027796 Neuralgias C1881674 Medical device emits smoke HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0037369 Smoking HSDN C0004941 Behavioral symptoms C1864923 Northern epilepsy syndrome OrphaNet C0085636 Light sensitivity C3151192 Leber congenital amaurosis 7 MalaCards|HPO C0003467 Angst C2674949 Chromosome 3q29 deletion syndrome MalaCards C1963281 Vomiting adverse event C1845862 Creatine deficiency, x-linked MalaCards|HPO C0018772 Deafness C0001430 Adenoma HSDN C4084768 Usual severity vomiting C0032266 Emphysema, intestinal HSDN C4084767 Bothered by vomiting C0022408 Arthropathy HSDN C4085211 Pain distress question C0001173 Adult pyloric stenosis HSDN C0233844 Awkwardness C1864923 Northern epilepsy syndrome OrphaNet|UMLS|HPO|MalaCards C0751837 Gait ataxic C1851481 Erythrokeratodermia with ataxia UMLS C4085862 Bothered by nausea C0023743 Linitis plastica HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C3150754 Glycogen storage disease xv MalaCards C1557397 Adverse event associated with pain C0040441 Broken teeth HSDN C1069915 Vertigo C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards C0013421 Dystonia C0026650 Movement disorders UMLS C0851578 Disorder sleep C0033873 Psychiatry HSDN C0151908 Dry skin C0043346 Xeroderma pigmentosum OrphaNet|HPO|MalaCards C0027497 Queasy C0035439 Rheumatic heart disease UMLS C0030552 Paralysis partial C0021051 Immunologic deficiency syndromes HSDN C0030193 Sense of pain C0042164 Uveitis HSDN C0007398 Catatonic C0016558 Forensic psychiatri HSDN C0013196 Drug induced abnormal pigmentation of skin C0549567 Pigmentation disorders UMLS C0043094 Weight gain C0009244 Behavioral cognitive therapy HSDN C0398650 Idiopathic thrombocytopenia purpura C0000833 Abscess HSDN C2169806 Tic C0011407 Necrotic pulp HSDN C3815497 Cough C0268250 Gaucher disease, type 2 (disorder) OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C3164344 Adult onset autosomal dominant leukodystrophy OrphaNet|HPO C0037763 Spasm C4042784 Feeding and eating disorders HSDN C0040034 Thrombocytopenia C3888004 Hermansky-pudlak syndrome 5 MalaCards C1963065 Apnea adverse event C1859711 Arthrogryposis multiplex congenita with whistling face MalaCards C0242936 Center pain C0035321 Retinal tear HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019101 Hemorrhagic fever with renal syndrome HSDN C0242670 Chronic vegetative state C0011581 Depressive disorder HSDN C0427068 Legs weakness C2676732 Spastic paraplegia 38, autosomal dominant (disorder) MalaCards C1963252 Tremor adverse event C2981150 Uranostaphyloschisis HSDN C3539890 Pelvic pain causes awakening at night C1704436 Peripheral arterial diseases HSDN C0344434 Atrial fibrillation ecg C0406817 Collagenoma, familial cutaneous MalaCards C0016199 Pain flank C0678050 Adrenocortical carcinoma, stage i UMLS C2911645 Weight loss adverse event C0042076 Urologic neoplasms HSDN C0034124 Pupillary disorder C0010034 Corneal diseases HSDN C0016382 Cutaneous vascular engorgement C1836284 Epidermolysis bullosa simplex with migratory circinate erythema OrphaNet|HPO C0518090 Frequency of pain question C0036412 Sclera HSDN C0042025 Urinary incontinence stress C0042018 Urinary calculi HSDN C3887638 Failure to thrive in infant C1865285 Megalencephaly cutis marmorata telangiectatica congenita OrphaNet|HPO C1963091 Diarrhea adverse event C0206062 Lung diseases, interstitial HSDN C3665492 Pigmentations C0153519 Malignant neoplasm of connective and other soft tissues, nos MalaCards C0020673 Hypothermia (central) (local) C0242488 Acute lung injury HSDN C4085549 Dizziness C1968848 Epilepsy, familial mesial temporal lobe MalaCards C0027497 Queasy C0022650 Kidney calculi HSDN C4084726 Distress cough C4042784 Feeding and eating disorders HSDN C1549543 Administration method - pain C0042974 Von willebrand disease HSDN C1963071 Back pain adverse event C0017152 Gastritis HSDN C0522224 Palsied C0042035 Urination disorders HSDN C0018772 Deafness C2936859 N syndrome MalaCards C0009806 Constipate C4225239 Desanto-shinawi syndrome UMLS C0012833 Dizzy C0025427 Mercury poisoning HSDN C0150055 Pain chronic C0037944 Spinal stenosis HSDN C3665347 Vision impaired C0221406 Pituitary-dependent cushing's disease HPO C0241137 Skin pallor C0273483 Cranial nerve injury HSDN C1961131 Cough adverse event C0206629 Pulmonary blastoma OrphaNet|HSDN|MalaCards C0015672 Decreased energy C0000735 Abdominal neoplasms HSDN C0034933 Abnormal reflexes C0024121 Lung neoplasms HSDN C0237326 Defecation pain C1859049 Cchs with hirschsprung disease MalaCards|HPO C0018777 Deafness, conductive C0041408 Turner syndrome HSDN C0162834 Hyperpigmentation C1846142 Hoyeraal-hreidarsson syndrome MalaCards C1963184 Nystagmus adverse event C1847836 Oculocutaneous albinism, type iv OrphaNet|HPO|MalaCards C0522224 Palsied C0233629 Thinking and speaking disturbances HSDN C4085210 Usual severity pain C1532253 Sedentary lifestyle HSDN C0009460 Communication impairment C2240378 Cleft palate on exam HSDN C0023012 Delay language C0684324 Deficiency of phosphoglycerate kinase MalaCards C4084768 Usual severity vomiting C1457883 Aggressive reaction HSDN C0030193 Sense of pain C0752130 Spinal cord ischemia HSDN C1963137 Hydrocephalus adverse event C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C4085210 Usual severity pain C0002312 Alpha-thalassemia HSDN C0013421 Dystonia C0011854 Diabetes mellitus, insulin-dependent HSDN C3641756 Have diarrhea C0040809 Patient refusal of treatment HSDN C0344315 Mood depressed C0010308 Congenital hypothyroidism OrphaNet C0184567 Pain acute C0005365 Bibliotherapy HSDN C0030552 Paralysis partial C0520946 Emotional hypersensitivity HSDN C4084727 Cough frequency C0206171 Community acquired infections HSDN C4084768 Usual severity vomiting C0025037 Meckel diverticulum HSDN C2024878 Cardiovascular surgery result: dyspnea C0039336 Gustatory sense HSDN C0000727 Abdomen acute C0032241 Pleuropneumonia HSDN C4084776 Weight loss C0235461 Androgen excess HSDN C1963252 Tremor adverse event C0004238 Atrial fibrillation HSDN C4084766 Vomiting C0006309 Brucellosis HSDN C3665347 Vision impaired C3715216 Retinitis pigmentosa 66 MalaCards C3898969 Have been vomiting C0029928 Ovarian diseases HSDN C4084784 Diarrhea C0018188 Granuloma HSDN C2911645 Weight loss adverse event C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0030975 Disorders perception C2267227 Bulimia nervosa HSDN C0013404 Respiratory difficulty C0034089 Pulmonary valve stenosis HSDN C0004604 Pain back C2706915 Language:-:point in time:^patient:- HSDN C0018681 Headache, cephalalgia C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0751837 Gait ataxic C0022893 Otitis interna HSDN C0036572 Convulsion C0025345 Menstruation disturbances HSDN C1549543 Administration method - pain C0019569 Hirschsprung disease HSDN C0036659 Sensation disorder C0751863 Lead poisoning, nervous system, adult HSDN C0013362 Dysarthrias C0028866 Oculomotor nerve paralysis HSDN C0030193 Sense of pain C1265748 Torsion HSDN C2984057 Have nausea C0235146 Emotionally high HSDN C0013604 Edematous C0005283 Beta thalassemia HSDN C0018784 Deafness sensorineural C0030297 Pancreatic neoplasm HSDN C0004093 Asthenia C0037286 Skin neoplasms HSDN C1549543 Administration method - pain C0019285 Diaphragmatic hernia traumatic HSDN C0036572 Convulsion C3541306 Plasmodium measurement HSDN C0024031 Back pain lower back C0015302 External exotoses HSDN C0010200 Cough symptom C0009241 Cognition disorders HSDN C4084725 Usual severity cough C0008728 Churg-strauss syndrome MalaCards C0018524 Hallucinate C0005119 Bereavement HSDN C1279888 Proteinuria of undiagnosed cause C0342749 Glycogen storage disease ic MalaCards|HPO C0011991 Loose stools C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0577568 Mass of urinary system structure C0041915 Urachus, cyst UMLS C4084769 Vomiting frequency C0007097 Carcinomas HSDN C0002965 Crescendo angina C3541306 Plasmodium measurement HSDN C0349588 Stature short C1836121 Al-gazali syndrome MalaCards C0003862 Pain joint C0005941 Bone diseases, developmental HSDN C1549543 Administration method - pain C0033586 Failure, prosthesis HSDN C0036572 Convulsion C0029888 Otitis media purulent HSDN C4085210 Usual severity pain C0009782 Connective tissue diseases HSDN C0460137 Push down or depress C3810230 Neurodegeneration with brain iron accumulation 6 MalaCards C0557874 Global developmental delay C3150914 Mitochondrial dna depletion syndrome 4b (mngie type) MalaCards|HPO C4084767 Bothered by vomiting C0004044 Asphyxia HSDN C0751837 Gait ataxic C1707400 Classic medulloblastoma UMLS C2237041 Shox gene with short stature C2675644 Niemann-pick disease, intermediate, with visceral involvement and rapid progression HPO C0017672 Pain tongue C2350521 Gustatory perception HSDN C0009421 Comatose C0016756 Fructose-1,6-diphosphatase deficiency MalaCards|HPO C4085222 Nausea C0997768 Glaucoma HSDN C4084775 Usual severity weight loss C0221056 Adult type dermatomyositis OrphaNet|HSDN|MalaCards C0026826 High muscle tone C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C0086565 Liver function abnormal C0085253 Adult-onset still disease MalaCards C0030552 Paralysis partial C0039145 Syringomyelia and syringobulbia HSDN C0018991 Paralysis one side of body C0018213 Graves disease HSDN C0030554 Abnormal sensation C0027819 Neuroblastoma HSDN C2362324 Pediatric obesity C0037313 Sleep HSDN C1961131 Cough adverse event C0520538 Tracheobronchopathia osteoplastica MalaCards C0033774 Skin pruritus C1514197 Polycythemia vera, polycythemic phase UMLS C1961131 Cough adverse event C0033968 Psychotherapeutic technique HSDN C0011168 Disorder deglutition C0206083 Myelinoclasis, central pontine MalaCards C0036572 Convulsion C0796232 Bohring syndrome OrphaNet|UMLS|HPO|MalaCards C2242996 Tingling C0042994 Vulvar diseases HSDN C0497247 Blood pressure elevation C0033845 Pseudotumor cerebri MalaCards C0085636 Light sensitivity C3552852 Retinitis pigmentosa 65 MalaCards C0013604 Edematous C0034882 Rectal diseases HSDN C0028738 Nystagmus C0796004 Kabuki make-up syndrome MalaCards|HPO C0011991 Loose stools C0031542 Phlebitis HSDN C0036572 Convulsion C1837713 Joubert syndrome 3 MalaCards C4085210 Usual severity pain C0040436 Dental erosion HSDN C4084776 Weight loss C0020545 Hypertension, renovascular HSDN C1963066 Joint pain adverse event C0152062 Spirillum minus DiseaseOntology|MalaCards C4084788 Have dizziness C0029882 Otitis media HSDN C1963281 Vomiting adverse event C0023473 Myeloid leukemia, chronic HSDN C0349588 Stature short C0018609 Hartnup disease MalaCards|HPO C4084776 Weight loss C0036457 Scrapie HSDN C0242936 Center pain C0033845 Pseudotumor cerebri HSDN C0018780 Frequencies hearing high loss C0206586 Endolymphatic hydrops HSDN C0018681 Headache, cephalalgia C1961100 Erectile dysfunction adverse event HSDN C4085549 Dizziness C0015674 Chronic fatigue syndrome HSDN C1557397 Adverse event associated with pain C0333355 Inflammatory disease of mucous membrane HSDN C4085642 Level of joint stiffness C0432291 Mandibuloacral dysostosis HPO C1549543 Administration method - pain C0003886 Arthrogryposis HSDN C0002965 Crescendo angina C1881674 Medical device emits smoke HSDN C0000727 Abdomen acute C0001125 Acidosis, lactic HSDN C0012833 Dizzy C0023470 Myeloid leukemia HSDN C0003862 Pain joint C0423690 Facet joint pain UMLS C3463815 Feel fatigue C1510428 Cerebral abscess HSDN C0013604 Edematous C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0015672 Decreased energy C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0018681 Headache, cephalalgia C0014836 Escherichia coli infections HSDN C3146279 Coma C0085096 Peripheral vascular diseases HSDN C0424755 Fever symptoms C0004763 Barrett esophagus HSDN C0027498 Nausea vomiting C2717757 Retinocochleocerebral vasculopathies MalaCards C4085549 Dizziness C0031212 Personality disorders HSDN C0002962 Angina C0032787 Postoperative complications HSDN C0036659 Sensation disorder C0206083 Myelinoclasis, central pontine HSDN C3887638 Failure to thrive in infant C4014954 Neutropenia, severe congenital, 6, autosomal recessive MalaCards C3274924 Have been coughing C0314657 Genetic predisposition HSDN C0030552 Paralysis partial C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4085862 Bothered by nausea C0028796 Dermatitis, occupational HSDN C0009421 Comatose C0001433 Adenoma, acidophil HSDN C0004134 Dyssynergia C0268581 Holocarboxylase synthetase deficiency MalaCards|HSDN|HPO C0234523 Apraxia, classic C0878576 Posterior leucoencephalopathy syndrome HSDN C0424755 Fever symptoms C0023521 Globoid cell leukodystrophy OrphaNet C0027066 Myoclonic jerking C1864651 Gaucher disease, atypical, due to saposin c deficiency HPO C0030193 Sense of pain C3273218 Invasive lobular breast carcinoma, tubulolobular variant UMLS C0149793 Transient monocular blindness C0007785 Cerebral infarction HSDN C4084767 Bothered by vomiting C0017612 Glaucoma, open-angle HSDN C0004134 Dyssynergia C4015728 Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset UMLS C0000737 Abdomen pain C0020443 Hypercholesterolemia HSDN|UMLS C0018926 Emesis bloody C0038463 Strongyloides infection HSDN C0013362 Dysarthrias C2675875 Chromosome 2p16.1 p15 deletion syndrome MalaCards C0030200 Intractable pain C0029456 Osteoporosis HSDN C0018681 Headache, cephalalgia C0001314 Acute disease HSDN C1963184 Nystagmus adverse event C0270724 Infantile neuroaxonal dystrophy OrphaNet|HPO C4084724 Usual severity constipation C0002989 Epithelioid hemangioma of skin HSDN C0018784 Deafness sensorineural C3150215 Chromosome 6q24-q25 deletion syndrome MalaCards C4085317 Diarrhea frequency C0018133 Graft-vs-host disease HSDN C0011175 Deficient fluid volume C1864498 Renal tubular acidosis, distal, autosomal recessive MalaCards|HPO C4084727 Cough frequency C0025063 Mediastinal neoplasms HSDN C1557397 Adverse event associated with pain C0042995 Vulvar neoplasms HSDN C0184567 Pain acute C0852077 Blood coagulation disorders, inherited HSDN C0151686 Growth retardation C0795843 12 ring syndrome MalaCards C0010200 Cough symptom C0034362 Q fever DiseaseOntology|MalaCards C0034933 Abnormal reflexes C0015923 Fetal alcohol syndrome HSDN C0231528 Muscle pain generalized C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C0013395 Indigestion C0428953 Ecg infarction myocardial HSDN C0033774 Skin pruritus C1274753 Linear atrophoderma of moulin MalaCards C0424755 Fever symptoms C0030328 Panniculitis, nodular nonsuppurative OrphaNet|MalaCards C1963086 Confusion adverse event C0034929 Reflex HSDN C0042798 Vision dim C3809482 Myopia 23, autosomal recessive MalaCards C2237041 Shox gene with short stature C3888138 Monosomy x MalaCards C0242936 Center pain C0033936 Psychoses, alcoholic HSDN C0003862 Pain joint C2936917 Infantile polyarteritis MalaCards C0426579 Anorexia symptom C0026780 Mumps MalaCards C0010200 Cough symptom C0019621 Histiocytosis, langerhans-cell HSDN C0038990 Sweats C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0497247 Blood pressure elevation C0003492 Aortic coarctation MalaCards C0518090 Frequency of pain question C0158328 Trigger finger HSDN C4084724 Usual severity constipation C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0243026 Generalized infection C0041188 Pyomyositis, tropical MalaCards C0042963 Symptoms vomiting C0004659 Bacteriuria HSDN C0700078 Deep tendon reflex decrease C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C4084774 Have weight loss C3273031 Hnec MalaCards C3641756 Have diarrhea C0334489 Pancreatoblastoma OrphaNet|MalaCards C2096293 Ent surgical result ear vertigo C0007137 Squamous cell carcinoma HSDN C4085210 Usual severity pain C0391889 Bony union HSDN C3670462 Pustular dermatitis C0021368 Inflammation UMLS C1963137 Hydrocephalus adverse event C0220658 Pfeiffer syndrome MalaCards|HPO C3463815 Feel fatigue C0041374 Tumor virus infections HSDN C0518090 Frequency of pain question C0018467 Habituation, psychophysiologic HSDN C3146279 Coma C0042138 Uterine neoplasms HSDN C0332573 Macula C0391826 Lhermitte-duclos disease MalaCards C1557397 Adverse event associated with pain C0021390 Inflammatory bowel diseases HSDN C1962972 Proteinuria adverse event C0030297 Pancreatic neoplasm HSDN C1279888 Proteinuria of undiagnosed cause C0010674 Cystic fibrosis HSDN C0042963 Symptoms vomiting C2981668 Stage iii distal bile duct cancer UMLS C0012569 Double vision C0027127 Myotonia congenita HSDN C0009806 Constipate C0010695 Cystocele HSDN C4085317 Diarrhea frequency C0011875 Diabetic angiopathies HSDN C1963281 Vomiting adverse event C1862892 Hereditary angioedema type ii HPO C1961131 Cough adverse event C0524799 Hyperlucent lung HSDN C0015672 Decreased energy C0150277 Meditations HSDN C0007814 Cerebrospinal fluid otorrhea C0030422 Extra-adrenal paraganglioma HSDN C4084776 Weight loss C0031212 Personality disorders HSDN C2203646 Jaundice C1142158 Hepatic vein occlusion MalaCards C0011175 Deficient fluid volume C0343068 Familial cold urticaria MalaCards|HPO C1557397 Adverse event associated with pain C0079840 Milk allergy HSDN C0018784 Deafness sensorineural C0220654 Meningeal carcinomatosis HSDN C4084727 Cough frequency C0276932 Schistosoma; intercalatum DiseaseOntology C0009421 Comatose C4049644 Depression HSDN C0018524 Hallucinate C1843792 Frontotemporal lobar degeneration with tdp43 inclusions, grn-related HPO C2024878 Cardiovascular surgery result: dyspnea C0152108 Suberosis DiseaseOntology C0022346 Yellow skin C0015414 Eye neoplasms HSDN C2919142 Short stature adverse event C4015080 Microcephaly 13, primary, autosomal recessive MalaCards C0234376 Tremor action C1847725 Spinocerebellar ataxia 15 MalaCards|UMLS C0000737 Abdomen pain C1762616 Meningioma, benign, no icd-o subtype HSDN C3463815 Feel fatigue C1853733 Hemochromatosis, type 4 MalaCards C2237041 Shox gene with short stature C0265289 Metaphyseal chondrodysplasia schmid type MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0870082 Hyperkeratosis HSDN C0004604 Pain back C0037305 Neoplasm, skull HSDN C0011991 Loose stools C0032285 Pneumonia HSDN|UMLS C0007859 Pain neck C0997768 Glaucoma HSDN C0000737 Abdomen pain C3541306 Plasmodium measurement HSDN C0013362 Dysarthrias C0037286 Skin neoplasms HSDN C4085210 Usual severity pain C0020445 Hypercholesterolemia, familial HSDN C3887638 Failure to thrive in infant C1855126 3-methylglutaconic aciduria type iv OrphaNet|MalaCards C0031911 Pigment deposition C0021367 Mammary ductal carcinoma MalaCards C1557397 Adverse event associated with pain C0003962 Ascites HSDN C0004604 Pain back C0040136 Thyroid neoplasm HSDN C0015672 Decreased energy C0013274 Patent ductus arteriosus HSDN C2203646 Jaundice C0024198 Lyme disease HSDN C0587246 Extremity weakness C2750537 Myopathy, actin, congenital, with cores HPO C0152459 Striae C0010481 Cushing syndrome OrphaNet|MalaCards C0424755 Fever symptoms C0027661 Neoplasms, hormone-dependent HSDN C4084802 Usual severity diarrhea C0000821 Threatened abortion HSDN C0013604 Edematous C0041466 Typhoid fever HSDN C0011206 Delirium acute C0034494 Rabies (disorder) DiseaseOntology|MalaCards C2237041 Shox gene with short stature C1968740 Glycogen storage disease iiib HPO C2024878 Cardiovascular surgery result: dyspnea C0175816 Cold hemagglutinin disease OrphaNet C0233514 Behavior abnormal C0162635 Angelman syndrome OrphaNet|MalaCards C0037383 Sneeze C0027651 Tumor HSDN C0013395 Indigestion C0018916 Hemangioma HSDN C1962972 Proteinuria adverse event C0032914 Pre-eclampsia HSDN C0018808 Murmur C0342881 Familial hypercholesterolemia - homozygous OrphaNet|HPO|MalaCards C0040822 D tremors C0795910 Cowchock syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0085298 Sudden cardiac death HSDN C3539896 Pelvic pain occurs with urination C0041311 Tuberculosis, female genital HSDN C2237041 Shox gene with short stature C1855477 Dahlberg borer newcomer syndrome OrphaNet|MalaCards C0026838 Spasticity muscle C4050613 Anxiety scale (basc-2) HSDN C0004941 Behavioral symptoms C0751918 Cockayne pelizaeus merzbacher disease MalaCards C0727671 Red cross toothache drops C0011854 Diabetes mellitus, insulin-dependent HSDN C0019214 Hepatosplenomegaly C1969106 Osteopetrosis, autosomal recessive 4 MalaCards|HPO C4085317 Diarrhea frequency C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0015672 Decreased energy C2239176 Liver carcinoma MalaCards|HSDN C4084726 Distress cough C0027726 Nephrotic syndrome HSDN C4084769 Vomiting frequency C1527258 Infantile paralysis MalaCards C0037763 Spasm C0160680 Carotid artery injury HSDN C4084726 Distress cough C2706915 Language:-:point in time:^patient:- HSDN C0013604 Edematous C1253937 Pericardial effusion HSDN C3494358 Characteristic, prodromal C1705812 Nci thesaurus role HSDN C0007758 Cerebellar ataxia C1859564 Bardet-biedl syndrome 3 HPO C0018926 Emesis bloody C1412000 Mesenteric vascular insufficiency HSDN C0020458 Hyperhydrosis C0022134 Islet cell adenoma MalaCards C0020455 Hypergammaglobulinemia C2984302 Leishmaniasis infection pathway HSDN C1961131 Cough adverse event C0015230 Exanthema HSDN C0022346 Yellow skin C3502107 Breastfeeding jaundice UMLS C3539022 Pelvic pain decreasing in severity C0033873 Psychiatry HSDN C0042571 Vertigo subjective C0243026 Sepsis HSDN C0522224 Palsied C0017185 Gastrointestinal neoplasms HSDN C1549543 Administration method - pain C1720830 Painful bladder syndrome OrphaNet|MalaCards C4084723 Constipation C4041080 Neurocognitive disorders HSDN C4084726 Distress cough C0027627 Neoplasm metastasis HSDN C0013421 Dystonia C2676466 Pontocerebellar hypoplasia type 2b HPO C0019209 Large liver C0023788 Whipple disease OrphaNet|MalaCards C0000786 Abortion spontaneous C0023092 Lassa fever OrphaNet|MalaCards C0231528 Muscle pain generalized C0029835 Other specified tularemia nos DiseaseOntology|MalaCards C0009763 Conjunctiva inflammation C3149378 Immunodeficiency, common variable, 1 MalaCards|HPO C0002962 Angina C0032963 Pregnancy complications, cardiovascular HSDN C0004134 Dyssynergia C1844933 Spinocerebellar ataxia, x-linked 4 MalaCards C0033774 Skin pruritus C0719659 Dandruff brand HSDN C4084723 Constipation C1547940 Specimen source codes - ulcer HSDN C2939430 Fear of the dark C0522192 Dark fear UMLS C4084775 Usual severity weight loss C0019372 Herpesviridae infections HSDN C4084768 Usual severity vomiting C0027583 Nematode infections HSDN C2984058 Have pain C0023976 Long qt syndrome HSDN C0036659 Sensation disorder C0020732 Iatrogenic disease HSDN C1962972 Proteinuria adverse event C0018798 Congenital heart defects HSDN C4085210 Usual severity pain C0025490 Mesonephroma HSDN C0030975 Disorders perception C0022758 Kap HSDN C1963086 Confusion adverse event C0162565 Acute intermittent porphyria HSDN C4085862 Bothered by nausea C0205770 Choroid plexus papilloma HPO C1963137 Hydrocephalus adverse event C1850321 Oeis complex MalaCards C0012569 Double vision C3541306 Plasmodium measurement HSDN C0004604 Pain back C0006434 Burn injury HSDN C0241210 Speaking delay C0795907 Conotruncal anomaly face syndrome MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0473583 Nevus elasticus HSDN C3665347 Vision impaired C3542026 Peroxisome biogenesis disorder 5b MalaCards C0518090 Frequency of pain question C0007274 Carotid artery thrombosis HSDN C0007166 Cardiac output decreased C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0018681 Headache, cephalalgia C1962971 Myocarditis adverse event HSDN C0497406 Over weight C0003467 Anxiety HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1720777 Functional laterality HSDN C0041657 Consciousness loss C0029944 Drug overdose HSDN C2237041 Shox gene with short stature C1834969 Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly HPO C0018524 Hallucinate C0035436 Rheumatic fever HSDN C2984058 Have pain C0700251 Brachial plexus neuropathies HSDN C0009763 Conjunctiva inflammation C1832241 Agammaglobulinemia due to early prob cell defect OrphaNet|HPO|MalaCards C0026821 Cramp C0344434 Atrial fibrillation ecg HSDN C0018772 Deafness C2004491 Cicatrix HSDN C1963065 Apnea adverse event C0027877 Neuronal ceroid-lipofuscinoses MalaCards C0857305 Thrombocytopenia purpura C0007361 Cat-scratch disease HSDN C4085211 Pain distress question C0003466 Anus, imperforate HSDN C4085210 Usual severity pain C0025160 Megacolon HSDN C0037315 Breathing disorder during sleeping C1096902 Infantile sialic acid storage disease MalaCards C4084802 Usual severity diarrhea C0016509 Dermatoses, foot HSDN C0022346 Yellow skin C0002796 Anaplasmataceae infection HSDN C1549543 Administration method - pain C0030521 Parathyroid neoplasms HSDN C0003962 Ascites C2931787 Intracardiac myxoma MalaCards C3641756 Have diarrhea C0018199 Granuloma, plasma cell HSDN C0575081 Abnormal gait C0752208 Pseudodystonia MalaCards C3887638 Failure to thrive in infant C1306856 Megaloblastic anemia due to inborn errors of metabolism MalaCards C0020673 Hypothermia (central) (local) C2984572 Malaria pathway HSDN C0026205 Pupillary constriction C0015310 Exotropia HSDN C3541349 Syncope C0039144 Syringomyelia HSDN C0023012 Delay language C3713418 Ppm-x syndrome MalaCards C0018772 Deafness C0265341 Rieger syndrome OrphaNet|HPO C2237041 Shox gene with short stature C2919796 Glycogen storage disease type ia OrphaNet|MalaCards C2237041 Shox gene with short stature C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0000737 Abdomen pain C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0009398 Color vision defects C0001432 Adenoma, chromophobe HSDN C0020673 Hypothermia (central) (local) C1563716 Thyroid dysgenesis HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0039786 Therapeutic communities HSDN C3665492 Pigmentations C0268363 Osteogenesis imperfecta type iv (disorder) MalaCards C0557874 Global developmental delay C3809414 Cortical dysplasia, complex, with other brain malformations 3 MalaCards C2919142 Short stature adverse event C0432442 Chromosome 18p deletion syndrome OrphaNet|MalaCards C0917816 Deficiency mental C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C1963091 Diarrhea adverse event C0032231 Pleurisy HSDN C0557874 Global developmental delay C3495483 Amish brittle hair syndrome MalaCards C0009421 Comatose C0030354 Papilloma HSDN C4084788 Have dizziness C0006430 Burning mouth syndrome HSDN C1963137 Hydrocephalus adverse event C0275859 Syphilis, congenital, early MalaCards C0030552 Paralysis partial C0023240 Legionellosis MalaCards C0009421 Comatose C0008626 Congenital chromosomal disease HSDN C0016927 Gag reflex C0023066 Laryngismus HSDN C0028738 Nystagmus C1855008 Mitochondrial complex ii deficiency MalaCards|HPO C0518090 Frequency of pain question C0238417 Scorpion sting HSDN C0022107 Fussiness C0220743 Childhood hypophosphatasia (disorder) MalaCards C2984058 Have pain C0028758 Bonding HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0920350 Autoimmune thyroiditis HSDN C1279888 Proteinuria of undiagnosed cause C0021818 Intervertebral disk displacement HSDN C0010520 Skin cyanosis C0005122 Beriberi HSDN C0332563 Papulae C0406555 Elastoderma OrphaNet|MalaCards C0040822 D tremors C0013990 Pathological accumulation of air in tissues HSDN C3539892 Pelvic pain in front C0012979 Canine disease HSDN C4085211 Pain distress question C0033348 Language program HSDN C0000737 Abdomen pain C2239176 Liver carcinoma MalaCards|UMLS C0027066 Myoclonic jerking C2711743 Febrile myoclonus UMLS C4042891 Sleep wake disorders C1546654 Specimen source codes - granuloma HSDN C0030552 Paralysis partial C0042510 Ventricular fibrillation HSDN C4085211 Pain distress question C0030653 Behavior, paternal HSDN C0016204 Fart C0016751 Hereditary fructose intolerance syndrome HSDN C0020538 Hbp C1260386 Glucocorticoid-remediable aldosteronism HPO C0004134 Dyssynergia C2936741 Syndrome xxyy MalaCards C4084725 Usual severity cough C0003467 Anxiety HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0034494 Rabies (disorder) HSDN C0036572 Convulsion C0270849 Extratemporal epilepsy UMLS C4084768 Usual severity vomiting C0040524 Septic toxemia HSDN C0030552 Paralysis partial C0041295 Tuberculoma HSDN C3887638 Failure to thrive in infant C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C0040485 Wryneck C0700251 Brachial plexus neuropathies HSDN C1549543 Administration method - pain C0085426 Gram-positive bacterial infections HSDN C0036572 Convulsion C3897755 Recurrent childhood fibrillary astrocytoma UMLS C0034155 Thrombotic thrombocytopenic purpura C0025202 Melanoma HSDN C0009806 Constipate C0409959 Osteoarthritis, knee HSDN C0242936 Center pain C0036130 Salpingitis HSDN C0018772 Deafness C1527231 Adrenomyeloneuropathy MalaCards|HPO C0424755 Fever symptoms C0012242 Digestive system disorders HSDN C0030193 Sense of pain C0018133 Graft-vs-host disease HSDN C0424755 Fever symptoms C0035335 Retinoblastoma HSDN C4084897 Sleep disturbance subordinate domain C1384514 Conn syndrome MalaCards C0003079 Pupillary inequality C0024950 Maxillary diseases HSDN C0042963 Symptoms vomiting C0002892 Anemia, pernicious HSDN C3146279 Coma C2188545 Anuria HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023067 Laryngitis HSDN C0027497 Queasy C0018916 Hemangioma HSDN C2024878 Cardiovascular surgery result: dyspnea C0038395 Streptococcal infections HSDN C4085317 Diarrhea frequency C0019159 Hepatitis a HSDN C0151686 Growth retardation C0795969 Cholestasis-pigmentary retinopathy-cleft palate syndrome MalaCards C0020672 Body temperature decreased C0017612 Glaucoma, open-angle HSDN C0518090 Frequency of pain question C0033324 Prognathism HSDN C1963170 Hypothermia adverse event C0020544 Renal hypertension HSDN C0242936 Center pain C0206694 Mucoepidermoid carcinoma HSDN C0522224 Palsied C0011875 Diabetic angiopathies HSDN C4084766 Vomiting C0042345 Varicosity HSDN C3641756 Have diarrhea C1636667 Disorder characterized by eosinophilia HSDN C1963281 Vomiting adverse event C0025472 Mesenteric vascular occlusion HSDN C0003862 Pain joint C0004935 Animal ethology HSDN C2984058 Have pain C0403447 Chronic kidney insufficiency HSDN C2984058 Have pain C0014549 Tonic-clonic epilepsy HSDN C0750394 Wbc low C3151443 Dyskeratosis congenita, autosomal dominant 2 MalaCards C0013395 Indigestion C0016470 Food allergy HSDN C0034933 Abnormal reflexes C0026850 Muscular dystrophy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011586 Three dimensional vision HSDN C4084723 Constipation C0026857 Musculoskeletal diseases HSDN C0015672 Decreased energy C3809369 Paroxysmal nocturnal hemoglobinuria 2 MalaCards|UMLS C1963071 Back pain adverse event C0030319 Panic disorder HSDN C4042891 Sleep wake disorders C0035334 Retinitis pigmentosa HSDN C0010200 Cough symptom C0206255 Malaria vaccine HSDN C0019079 Bloody sputum C0206732 Epithelioid hemangioendothelioma HSDN C0013404 Respiratory difficulty C0017563 Gingival diseases HSDN C0018772 Deafness C0796094 Blepharophimosis syndrome ohdo type MalaCards C0039070 Collapse fleeting C0027666 Neoplasms, radiation-induced HSDN C4084768 Usual severity vomiting C0030330 Panniculitis, peritoneal HSDN C3539890 Pelvic pain causes awakening at night C0033575 Prostatic diseases HSDN C0027796 Neuralgias C0039223 Tabes dorsalis HSDN C4085210 Usual severity pain C0030783 Pellagra HSDN C0015230 Exanthem C1276070 Infantile atopic dermatitis UMLS C2984058 Have pain C0019154 Hepatic vein thrombosis HSDN C0011991 Loose stools C3809882 Neuropathy, hereditary sensory and autonomic, type vii MalaCards|UMLS C3146279 Coma C0032342 Rhus dermatitis HSDN C0019209 Large liver C0175816 Cold hemagglutinin disease MalaCards C0033790 Pseudobulbar palsy C0007760 Cerebellar diseases HSDN C3815497 Cough C0036946 Sheep--diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206694 Mucoepidermoid carcinoma HSDN C0277794 Exhaustion extreme C0152936 Plague, septicemic DiseaseOntology|MalaCards C0234132 Pyramidal sign C1850053 Pelizaeus-merzbacher-like disease, autosomal recessive, 2 MalaCards|HPO|UMLS C0013604 Edematous C0007095 Carcinoid tumor HSDN C0009421 Comatose C0268542 Ornithine carbamoyltransferase deficiency HPO C0413252 Hypothermia due to exposure C1299262 Sarcoma - category (morphologic abnormality) HSDN C0018784 Deafness sensorineural C0554634 Syphilis, congenital, late MalaCards C0009024 Clonus C1847582 Lipodystrophy with congenital cataracts and neurodegeneration HPO C0022346 Yellow skin C1333504 Cystadenoma of extrahepatic bile duct UMLS C2024893 Cardiovascular surgery result: fatigue C0035439 Rheumatic heart disease HSDN C3146279 Coma C0022658 Kidney diseases HSDN C0015672 Decreased energy C0016542 Foreign body HSDN C2984057 Have nausea C3888013 Hypnoses HSDN C0576456 Poor feeding C1838979 Mitochondrial complex i deficiency MalaCards C0242936 Center pain C0007774 Cerebral arterial diseases HSDN C1963065 Apnea adverse event C1864910 Glutamine deficiency, congenital MalaCards|HPO C0018834 Brash C0021603 Sleep initiation and maintenance disorders HSDN C0030193 Sense of pain C0175702 Williams syndrome HSDN C0557874 Global developmental delay C0948368 Kaufman-mckusick syndrome MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0020635 Hypopituitarism HSDN C0009792 Consciousness disorder C0015464 Facial nerve diseases HSDN C0040822 D tremors C0024141 Lupus erythematosus, systemic HSDN C1962972 Proteinuria adverse event C2711227 Steatohepatitis HSDN C0349506 Sun sensitivity C0342859 Harderoporphyria HPO C0007815 Cerebrospinal fluid rhinorrhoea C0024141 Lupus erythematosus, systemic HSDN C0349588 Stature short C2931125 Feigenbaum bergeron richardson syndrome OrphaNet|MalaCards C2029884 Hearing loss by exam C0796279 Carnevale syndrome MalaCards C0020578 Hyperventilate C0520679 Sleep apnea, obstructive HSDN C3887873 Hearing loss C2350521 Gustatory perception HSDN C0036396 Sciatica C0007462 Causalgia syndrome HSDN C0231528 Muscle pain generalized C0014804 Erythromelalgia HSDN C4084784 Diarrhea C1849236 Severe combined immunodeficiency, atypical HPO C3539022 Pelvic pain decreasing in severity C0041954 Ureteral diseases and syndromes HSDN C0027424 Congestion nasal C0149980 Rhinitis medicamentous UMLS C4084775 Usual severity weight loss C0027666 Neoplasms, radiation-induced HSDN C0085636 Light sensitivity C1848412 Trichothiodystrophy with sun sensitivity HPO C2315100 Pediatric failure to thrive C0008925 Cleft palate HSDN C2024878 Cardiovascular surgery result: dyspnea C0035468 Scleroma HSDN C0002962 Angina C1527336 Sjogren's syndrome HSDN C1963091 Diarrhea adverse event C0023343 Leprosy HSDN C0700590 Diaphoresis excessive C1859468 Bird headed dwarfism montreal type OrphaNet|MalaCards C4084724 Usual severity constipation C0026650 Movement disorders HSDN C0022346 Yellow skin C0007965 Chediak-higashi syndrome MalaCards|HPO|UMLS C0009806 Constipate C0030305 Pancreatitis HSDN|UMLS C3274924 Have been coughing C0684249 Carcinoma of lung DiseaseOntology C0030486 Extremity paralysis, lower C0018798 Congenital heart defects HSDN C4085317 Diarrhea frequency C0007193 Cardiomyopathy, dilated HSDN C4084802 Usual severity diarrhea C0005586 Bipolar disorder HSDN C0018772 Deafness C0796013 Zimmerman laband syndrome MalaCards C0036572 Convulsion C0000833 Abscess HSDN C0013390 Cramps menstrual C1963138 Hypertension adverse event HSDN C0023530 Leukopenia C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0002448 Ameloblastoma HSDN C0518090 Frequency of pain question C0042510 Ventricular fibrillation HSDN C0018772 Deafness C1832334 Charcot-marie-tooth disease, type 4d MalaCards|HPO C0011991 Loose stools C1850406 Navajo neurohepatopathy MalaCards|HPO|UMLS C0020450 Hyperemesis gravidarum C0544566 Hyperemesis gravidarum, severe UMLS C4084766 Vomiting C0023269 Leiomyosarcoma HSDN C2911645 Weight loss adverse event C0026946 Mycoses HSDN C0151205 Periorbital edema C0011633 Dermatomyositis OrphaNet|MalaCards C0020580 Decreased sensation C0024299 Lymphoma HSDN C2919142 Short stature adverse event C4014942 Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia MalaCards C3898969 Have been vomiting C2717979 Tooth wear HSDN C0030193 Sense of pain C1705812 Nci thesaurus role HSDN C0029163 Hemorrhage mouth C0020635 Hypopituitarism HSDN C0022346 Yellow skin C0004275 Attitude health HSDN C0030193 Sense of pain C0024301 Lymphoma, follicular HSDN C0003467 Angst C2678416 Hyperphenylalaninemia, non-pku mild HPO C1963087 Constipation adverse event C0221069 Anterior spinal artery syndrome HSDN C0018524 Hallucinate C0026650 Movement disorders HSDN C0231218 Malaise generalized C0854832 Angiocentric lymphoma refractory UMLS C0151315 Neck rigid C0014060 Encephalitis, st. louis DiseaseOntology|MalaCards C0027498 Nausea vomiting C0153413 Malignant neoplasm of upper third of esophagus MalaCards C0004134 Dyssynergia C0520679 Sleep apnea, obstructive HSDN C0042928 Paralysis vocal cord C1261473 Sarcoma HSDN C0002965 Crescendo angina C0033817 Pseudomonas infections HSDN C0008031 Pain chest C0006840 Candidiasis HSDN C0007758 Cerebellar ataxia C0015458 Facial hemiatrophy MalaCards C0242936 Center pain C0020503 Hyperparathyroidism, secondary HSDN C0028738 Nystagmus C0162809 Kallmann syndrome OrphaNet|HPO|MalaCards C0577698 Angina exertional C0027051 Myocardial infarction UMLS C0027796 Neuralgias C0025500 Mesothelioma HSDN C2911647 Weight gain adverse event C0439840 Reflex motion descriptor HSDN C0221166 Paraparesis C0475073 Subarachnoid hemorrhage traumatic HSDN C4084769 Vomiting frequency C0011334 Dental caries HSDN C0013404 Respiratory difficulty C0039336 Gustatory sense HSDN C0015672 Decreased energy C0041948 Uremia HSDN C0151786 Weakness muscle C3151403 Amyotrophic lateral sclerosis 14 with or without frontotemporal dementia HPO C4085211 Pain distress question C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C0018772 Deafness C0039082 Syndrome HSDN C4085661 Usual severity nausea C0019348 Herpes simplex infections HSDN C0036572 Convulsion C0001396 Stokes-adams syndrome HSDN C2237041 Shox gene with short stature C1866719 Spondyloepiphyseal dysplasia, myopia, and sensorineural deafness MalaCards C4084769 Vomiting frequency C1963088 Cystitis adverse event HSDN C0850758 Pain pelvic C0035358 Retroperitoneal neoplasm HSDN C0039070 Collapse fleeting C0019372 Herpesviridae infections HSDN C1565249 Limitation, mobility C0025312 Meningomyelocele HSDN C1962972 Proteinuria adverse event C0036117 Salmonella infections HSDN C2203646 Jaundice C0032371 Poliomyelitis HSDN C4084775 Usual severity weight loss C0035012 Reiter syndrome MalaCards C0036572 Convulsion C0234978 Epilepsy, jacksonian UMLS C1963170 Hypothermia adverse event C0015802 Femur fracture HSDN C0020580 Decreased sensation C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0033774 Skin pruritus C0011849 Diabetes mellitus HSDN C4084774 Have weight loss C0040411 Tongue neoplasms HSDN C1519353 Skin eruption papular C1275122 Familial multiple trichoepitheliomata OrphaNet|HPO|MalaCards C1527344 Dysphonia C0085655 Polymyositis MalaCards C2029884 Hearing loss by exam C0029422 Osteochondrodysplasias HSDN C0162835 Hypopigmentation C3537440 Cystinosis, infantile nephropathic MalaCards C3887638 Failure to thrive in infant C2745948 Hyalinosis, systemic MalaCards C0557874 Global developmental delay C2677613 Chromosome 15q13.3 microdeletion syndrome OrphaNet|HPO C1962972 Proteinuria adverse event C0003125 Anorexia nervosa HSDN C3539022 Pelvic pain decreasing in severity C0206687 Carcinoma, endometrioid HSDN C1963091 Diarrhea adverse event C1833454 Komuragaeri disease MalaCards C4084766 Vomiting C1833104 Diabetes mellitus, permanent neonatal MalaCards C3539889 Pelvic pain increasing in severity C0038478 Struma ovarii HSDN C0522224 Palsied C0016719 Friedreich ataxia HSDN C1963091 Diarrhea adverse event C0003504 Aortic valve insufficiency HSDN C0002962 Angina C0023890 Liver cirrhosis HSDN C0454644 Delayed language development C1412749 Bbs4 gene HPO C3641755 Have constipation C0342613 Danish type familial amyloid cardiomyopathy MalaCards C3539892 Pelvic pain in front C0206654 Leiomyomatosis HSDN C3539022 Pelvic pain decreasing in severity C0019553 Contracture hips HSDN C1961131 Cough adverse event C0950123 Inborn genetic disease HSDN C0013404 Respiratory difficulty C1839884 Leiomyomatosis, esophageal and vulval, with nephropathy UMLS C3539891 Pelvic pain to the rear C0038160 Staphylococcal infections HSDN C0264345 Smoker cough C0024115 Lung diseases UMLS C0020672 Body temperature decreased C0878544 Cardiomyopathies HSDN C4084766 Vomiting C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C0521788 Crackling ear sounds C0260662 Hearing problem UMLS C0022346 Yellow skin C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C0020672 Body temperature decreased C0010068 Coronary heart disease HSDN C0151908 Dry skin C0032339 Rothmund-thomson syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C0021890 Intraoperative complications HSDN C0003862 Pain joint C3714605 Of pain perception HSDN C0235299 Abdomen ruq pain C0748758 Skin cancer malignant melanoma metastatic UMLS C0035232 Diaphragmatic paralysis C1963138 Hypertension adverse event HSDN C4084802 Usual severity diarrhea C0027830 Neurofibroma HSDN C3898969 Have been vomiting C0037379 Snake bite HSDN C1963091 Diarrhea adverse event C0032460 Polycystic ovary syndrome HSDN C4084768 Usual severity vomiting C0004933 Behavior modification technique HSDN C4084726 Distress cough C0042075 Urologic diseases HSDN C4084726 Distress cough C0006288 Bronchopulmonary sequestration HSDN C3539020 Pelvic pain decreasing in frequency C0085222 Psoas muscle abscess HSDN C4084802 Usual severity diarrhea C0016627 Avian influenza DiseaseOntology|HSDN|MalaCards C1963071 Back pain adverse event C2984572 Malaria pathway HSDN C2911647 Weight gain adverse event C0023891 Liver cirrhosis, alcoholic HSDN C0242936 Center pain C1963107 Euphoria adverse event HSDN C0085636 Light sensitivity C0997768 Glaucoma HSDN C0917816 Deficiency mental C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C4084776 Weight loss C0041312 Tuberculosis git nos DiseaseOntology|HSDN|MalaCards C1963087 Constipation adverse event C0175693 Russell-silver syndrome MalaCards C4085210 Usual severity pain C0027086 Myoma HSDN C0917816 Deficiency mental C2931050 Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies OrphaNet C0151889 Reflexes tendon increased C3810326 Spinocerebellar ataxia, autosomal recessive 15 MalaCards C0024031 Back pain lower back C0032964 Pregnancy complications, hematologic HSDN C0232461 Increased appetite C1846171 Lissencephaly, x-linked, 2 MalaCards C1963087 Constipation adverse event C0348018 Projections HSDN C1963137 Hydrocephalus adverse event C1842462 Campomelic dysplasia with autosomal sex reversal HPO C2984058 Have pain C0085084 Motor neuron disease HSDN C2911647 Weight gain adverse event C0016510 Foot diseases HSDN C1961131 Cough adverse event C3463824 Myelodysplastic syndrome HSDN C4085548 Usual severity dizziness C0007781 Intracranial embolism and thrombosis HSDN C0042420 Vasovagal episode C0018944 Hematoma HSDN C0013362 Dysarthrias C1719788 Episodic ataxia type 1 HPO C0007166 Cardiac output decreased C0036946 Sheep--diseases HSDN C0424755 Fever symptoms C0031090 Periodontal diseases HSDN C0002622 Amnesias C0016563 Form perception HSDN C4084776 Weight loss C0018567 Hand dermatoses HSDN C0424755 Fever symptoms C2706915 Language:-:point in time:^patient:- HSDN C1963170 Hypothermia adverse event C0042345 Varicosity HSDN C0518090 Frequency of pain question C0085094 Head injury closed HSDN C0221166 Paraparesis C0206716 Ganglioglioma HSDN C2024893 Cardiovascular surgery result: fatigue C0005940 Bone diseases HSDN C0007758 Cerebellar ataxia C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0013604 Edematous C0022876 Premature obstetric labor HSDN C4085642 Level of joint stiffness C3839326 Kuskokwim syndrome MalaCards C0010200 Cough symptom C0023241 Legionnaires' disease OrphaNet|MalaCards C0085636 Light sensitivity C0241802 Arthritis, venereal MalaCards C0151686 Growth retardation C1855396 Alpha mannosidosis, type ii HPO C0497406 Over weight C0007570 Celiac disease HSDN C0018524 Hallucinate C0023903 Liver neoplasms HSDN C4085210 Usual severity pain C0023487 Acute promyelocytic leukemia HSDN C0004604 Pain back C3146297 Study of behavior during childhood HSDN C0242936 Center pain C0037116 Silicosis HSDN C1963086 Confusion adverse event C0015230 Exanthema HSDN C1557397 Adverse event associated with pain C0032269 Pneumococcal infections HSDN C0034150 Skin purpura C0409818 Chronic infantile neurological, cutaneous, and articular syndrome MalaCards|HPO C4020887 Photodysphoria C1842914 Adult-onset vitelliform macular dystrophy MalaCards|HPO C0020455 Hypergammaglobulinemia C0024530 Malaria HSDN C0018991 Paralysis one side of body C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO|UMLS C3641755 Have constipation C0041296 Tuberculosis HSDN C0426579 Anorexia symptom C2706915 Language:-:point in time:^patient:- HSDN C2025995 Cellulitis C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards C0033774 Skin pruritus C2987166 Pancreatic medullary carcinoma UMLS C3641755 Have constipation C3827868 Tachycardia by ecg finding HSDN C4084768 Usual severity vomiting C0004626 Pneumonia, bacterial HSDN C3641755 Have constipation C3281084 Congenital disorder of glycosylation, type ir MalaCards C0013362 Dysarthrias C0002871 Anemia HSDN C3539890 Pelvic pain causes awakening at night C0520676 Premenstrual dysphoric disorder HSDN C0749870 Upper motor neuron sign C3807521 Amyotrophic lateral sclerosis 21 MalaCards|UMLS C0013421 Dystonia C1706377 Memory device component HSDN C4084725 Usual severity cough C0036231 Sarcocystosis DiseaseOntology C1963137 Hydrocephalus adverse event C0796117 Pitt syndrome MalaCards C0518090 Frequency of pain question C0751895 Vasospasm, intracranial HSDN C0151786 Weakness muscle C0079541 Holoprosencephaly OrphaNet|MalaCards C0700078 Deep tendon reflex decrease C3279775 Multiple congenital anomalies-hypotonia-seizures syndrome 1 MalaCards C0018777 Deafness, conductive C1838652 Split-hand/foot malformation 3 MalaCards C0015672 Decreased energy C1423541 Vangl2 gene HSDN C0424755 Fever symptoms C0039144 Syringomyelia HSDN C0019572 Hairiness C3281247 Bent bone dysplasia syndrome MalaCards C0234132 Pyramidal sign C2828721 Spastic paraplegia 46, autosomal recessive MalaCards|UMLS C4085211 Pain distress question C0085417 Epilepsy, complex partial HSDN C4085549 Dizziness C0027643 Neoplasm recurrence, local HSDN C0018772 Deafness C3888138 Monosomy x MalaCards C0020538 Hbp C0403443 Renal failure, progressive, with hypertension MalaCards C0518090 Frequency of pain question C0033968 Psychotherapeutic technique HSDN C3463815 Feel fatigue C0343633 Brazilian haemorrhagic fever MalaCards C0007758 Cerebellar ataxia C1261473 Sarcoma HSDN C0020505 Excessive eating C0032897 Prader-willi syndrome MalaCards|HPO C0013404 Respiratory difficulty C2984291 Glioblastoma multiforme pathway HSDN C4085211 Pain distress question C0026948 Mycosis fungoides HSDN C0020796 Profoundly mentally retarded C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome MalaCards C0026961 Pupil dilated C4024770 Bilateral congenital mydriasis UMLS C2132198 Abnormal blistering of the skin C1274700 Postmenopausal frontal fibrosing alopecia MalaCards C0020673 Hypothermia (central) (local) C0264766 Rheumatic mitral stenosis HSDN C0003862 Pain joint C0011119 Decompression sickness HSDN C4084768 Usual severity vomiting C0021783 Internal external locus of control HSDN C4050613 Anxiety C1834570 Myoclonic dystonia HPO C0018681 Headache, cephalalgia C1334236 Intracerebral cystic meningioma UMLS C2073301 Chest pain localizing to right anterior chest wall C0877023 Chest pain intercostal UMLS C0027796 Neuralgias C0041327 Tuberculosis, pulmonary HSDN C1963252 Tremor adverse event C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0237326 Defecation pain C0001529 Dercum disease MalaCards C0018772 Deafness C0019196 Hepatitis c HSDN C0162298 Stiffness joints C2931282 Skeletal dysplasia, san diego type MalaCards|HPO C0013604 Edematous C1704275 Pyomyositis HSDN C0030975 Disorders perception C1962986 Glaucoma adverse event HSDN C3815497 Cough C0011875 Diabetic angiopathies HSDN C3887784 Decreased urine output C0003486 Aortic aneurysm HSDN C3641755 Have constipation C0206245 Amyloid neuropathies, familial MalaCards|HSDN C0151786 Weakness muscle C4024961 Metachromatic leukodystrophy variant MalaCards C0427055 Face weakness C1865143 Branchiootic syndrome 1 MalaCards C2169806 Tic C0035258 Restless legs syndrome HSDN C0015402 Hemorrhage eye C0238045 Carotid artery-cavernous sinus fistula HSDN C4084769 Vomiting frequency C0026848 Myopathy HSDN C0004604 Pain back C1636667 Disorder characterized by eosinophilia HSDN C0007398 Catatonic C0027932 Neurotic disorders HSDN C4084774 Have weight loss C0033975 Psychotic disorders HSDN C0009792 Consciousness disorder C0021670 Insulinoma HSDN C0013404 Respiratory difficulty C0150034 Exchange gas impaired UMLS C0727671 Red cross toothache drops C0029293 Oroantral fistula HSDN C2984057 Have nausea C0206715 Neoplasms, neuroepithelial HSDN C4084802 Usual severity diarrhea C0013504 Echinococcosis, hepatic HSDN C0518090 Frequency of pain question C0031094 Periodontal pocket HSDN C4085317 Diarrhea frequency C0033953 Psychosexual disorders HSDN C1963274 Vasculitis adverse event C0524988 Schnitzler syndrome MalaCards C1962972 Proteinuria adverse event C0162671 Melas syndrome MalaCards|HPO C3539023 Pelvic pain increasing in frequency C0221752 Rbc urine HSDN C1962972 Proteinuria adverse event C2937358 Cerebral hemorrhage HSDN C0851578 Disorder sleep C0008925 Cleft palate HSDN C1510417 Apraxia of gait C0027658 Neoplasms, germ cell and embryonal HSDN C3898969 Have been vomiting C0009240 Cognition HSDN C0399591 Sublingual sialectasia C0410013 Soft tissue lesion UMLS C1961131 Cough adverse event C0010346 Crohn disease HSDN C0009421 Comatose C0220710 Medium-chain acyl-coenzyme a dehydrogenase deficiency HPO C0036572 Convulsion C3899674 Childhood brain oligodendroglioma UMLS C0032617 High urine output C0221002 Hyperparathyroidism, primary HSDN C0022346 Yellow skin C2930674 Babesioses, human MalaCards C0917816 Deficiency mental C2931646 Oculocerebral hypopigmentation syndrome type preus OrphaNet|MalaCards C1961131 Cough adverse event C0017416 Genital neoplasms, female HSDN C0014089 Functional encopresis C0036039 Sadism HSDN C0018524 Hallucinate C0008066 Child behavior disorders HSDN C0030554 Abnormal sensation C0033968 Psychotherapeutic technique HSDN C3146279 Coma C0030354 Papilloma HSDN C1963091 Diarrhea adverse event C0014805 Primary erythermalgia MalaCards|HPO C0231528 Muscle pain generalized C0041188 Pyomyositis, tropical OrphaNet|HSDN|MalaCards C2032741 Mouth sore painless C0149745 Oral ulcer UMLS C4084766 Vomiting C0085277 Munchausen by proxy syndrome HSDN C0019825 Voice hoarseness C0220726 Diastrophic dysplasia MalaCards|HPO C0018520 Breath odor C0043352 Xerostomia UMLS C0860603 Anxiety symptom C2936741 Syndrome xxyy OrphaNet|MalaCards C2203646 Jaundice C0035222 Respiratory distress syndrome, adult HSDN C1963170 Hypothermia adverse event C0003838 Arterial occlusive diseases HSDN C0917816 Deficiency mental C2677590 Congenital disorder of glycosylation, type in MalaCards|HPO C3665492 Pigmentations C1332614 Angiosarcoma of the breast MalaCards C0022408 Disorder joint C2931645 Ochronosis, hereditary MalaCards C0027497 Queasy C0004364 Autoimmune diseases HSDN C0007859 Pain neck C0001828 Agricultural workers' diseases HSDN C2984058 Have pain C1963088 Cystitis adverse event HSDN C0010200 Cough symptom C0020456 Hyperglycemia HSDN C3887638 Failure to thrive in infant C1865644 Plantar lipomatosis, unusual facies, and developmental delay MalaCards|HPO C0033774 Skin pruritus C0005779 Blood coagulation disorders HSDN C4084921 Usual severity itching C0019360 Herpes zoster disease DiseaseOntology|MalaCards C1963252 Tremor adverse event C0268242 Niemann-pick disease, type a MalaCards|HSDN C4084776 Weight loss C0598402 Animal migration HSDN C0231807 Dyspnea exertional C0392775 Cystic medial necrosis of aorta OrphaNet|HPO|MalaCards C0015672 Decreased energy C0003869 Arthritis, infectious HSDN C0878753 Unspecified lack of expected normal physiological development in childhood C0810255 Other and unspecified metabolic; nutritional; and endocrine disorders UMLS C4085211 Pain distress question C0018206 Granulosa cell tumor HSDN C2315100 Pediatric failure to thrive C3151097 Meier-gorlin syndrome 2 MalaCards|HPO C1549543 Administration method - pain C0021603 Sleep initiation and maintenance disorders HSDN C4084725 Usual severity cough C0039483 Giant cell arteritis MalaCards|HPO C4084802 Usual severity diarrhea C0268124 Adenosine deaminase deficiency MalaCards C0497406 Over weight C0242659 Female homosexual HSDN C3898969 Have been vomiting C2936913 Porphyria, south african type HPO C0270327 Bed wetting C0175702 Williams syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0009062 Clostridia infection HSDN C0518090 Frequency of pain question C0023772 Lipid metabolism, inborn errors HSDN C1963281 Vomiting adverse event C0007125 Carcinoma, ehrlich tumor HSDN C0031911 Pigment deposition C0524801 Retinal neoplasms MalaCards C0018834 Brash C0268341 Ehlers-danlos syndrome type 5 OrphaNet|MalaCards C1557397 Adverse event associated with pain C0026590 Child mother relationship HSDN C1963252 Tremor adverse event C0270733 Striatonigral degeneration HSDN C2029744 Headache preceded by one leg or arm tingling or going numb C0030554 Paresthesia UMLS C4084774 Have weight loss C0013808 Electroconvulsive therapy HSDN C0011175 Deficient fluid volume C0043395 Yellow fever MalaCards C4084784 Diarrhea C0042214 Vaccinia HSDN C0015300 Ocular proptosis C1853554 Radiation induced meningioma MalaCards C0237326 Defecation pain C1834877 Holoprosencephaly 2 (disorder) HPO C4084784 Diarrhea C0005716 Blastomycosis HSDN C3887873 Hearing loss C1861922 Campomelic dysplasia MalaCards C0242936 Center pain C0221269 Pseudolymphoma HSDN C4085317 Diarrhea frequency C0022373 Disease, jejunal HSDN C0151786 Weakness muscle C0305062 Tetanus toxoids HSDN C0030552 Paralysis partial C0036161 Sandhoff disease OrphaNet|HPO C0162835 Hypopigmentation C2718078 Deficiency of uroporphyrinogen iii synthase MalaCards|HPO C1963170 Hypothermia adverse event C1299262 Sarcoma - category (morphologic abnormality) HSDN C4084776 Weight loss C0032965 Pregnancy complications, infectious HSDN C0042963 Symptoms vomiting C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0013604 Edematous C1299262 Sarcoma - category (morphologic abnormality) HSDN C0013421 Dystonia C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0600040 Chronic interstitial cystitis OrphaNet C0750394 Wbc low C1135161 Stage 4s neuroblastoma MalaCards C3898969 Have been vomiting C0752132 Infarction, pca HSDN C0518090 Frequency of pain question C0376154 Skin callus HSDN C2024893 Cardiovascular surgery result: fatigue C0011882 Diabetic neuropathies HSDN C0010200 Cough symptom C0041321 Tuberculosis, miliary HSDN C0036572 Convulsion C0039841 Thiamine deficiency HSDN C0026826 High muscle tone C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO C0973461 Dysphasia C2720163 Placental steroid sulfatase deficiency MalaCards C0085602 Polydypsia C1563705 Nephrogenic diabetes insipidus, type i HPO|UMLS C0015230 Exanthem C0410422 Chronic multifocal osteomyelitis MalaCards C0700590 Diaphoresis excessive C3150809 Ectodermal dysplasia-syndactyly syndrome 2 MalaCards C4085211 Pain distress question C0001618 Tumors of adrenal cortex HSDN C0424755 Fever symptoms C0020621 Hypokalemia HSDN C1963087 Constipation adverse event C0038160 Staphylococcal infections HSDN C3463815 Feel fatigue C0025500 Mesothelioma HSDN C0030193 Sense of pain C0277509 Epidemic cervical myalgia UMLS C0750394 Wbc low C1535942 Autoimmune polyglandular syndrome type iii MalaCards C0518090 Frequency of pain question C0334299 Carcinoid tumor no icd-o subtype HSDN C0850758 Pain pelvic C0015732 Fecal incontinence HSDN C4050613 Anxiety C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C0036659 Sensation disorder C0812393 Cancer patients and suicide and depression HSDN C1961131 Cough adverse event C0004031 Aspergillosis, allergic bronchopulmonary DiseaseOntology|OrphaNet|MalaCards C4084788 Have dizziness C0010709 Cyst HSDN C4085211 Pain distress question C0872996 Q fever vaccine HSDN C2203646 Jaundice C0033700 Infection proteus HSDN C1963065 Apnea adverse event C0011581 Depressive disorder HSDN C0162292 Extraocular palsy C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO C0028738 Nystagmus C1841721 Achromatopsia 4 HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C3203102 Idiopathic pulmonary arterial hypertension OrphaNet C0035078 Failure kidney C0587248 Costello syndrome (disorder) MalaCards|HPO C1963065 Apnea adverse event C0022658 Kidney diseases HSDN C0018784 Deafness sensorineural C0343068 Familial cold urticaria MalaCards|HPO C3898969 Have been vomiting C1548484 Rheumatic fever vaccine HSDN C1549543 Administration method - pain C0035328 Retinal vein occlusion HSDN C4085317 Diarrhea frequency C2931402 Lubani al saleh teebi syndrome OrphaNet|MalaCards C2237041 Shox gene with short stature C1563706 Nephrogenic diabetes insipidus, type ii HPO C0002962 Angina C0034194 Pyloric stenosis HSDN C0020673 Hypothermia (central) (local) C0007131 Non-small cell lung carcinoma HSDN C4084767 Bothered by vomiting C2963140 Arteriovenous fistula in use with two needles HSDN C4084784 Diarrhea C0002170 Alopecia HSDN C2029884 Hearing loss by exam C0002726 Amyloidosis HSDN C0036572 Convulsion C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C1962972 Proteinuria adverse event C0034063 Pulmonary edema HSDN C0151603 Edema generalized C0024620 Primary malignant neoplasm of liver MalaCards C0007384 Cataplexy C1836907 Narcolepsy 3 MalaCards C1963087 Constipation adverse event C0008628 Chromosome deletion HSDN C2219716 Missed most recent menstrual period C0025345 Menstruation disturbances UMLS C2919142 Short stature adverse event C1848068 Mental retardation, x linked, with isolated growth hormone deficiency HPO C0206160 Retic count elevated C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C4084727 Cough frequency C0023048 Creeping eruptions HSDN C0454644 Delayed language development C1848488 Pierre robin syndrome with fetal chondrodysplasia OrphaNet|HPO C0020673 Hypothermia (central) (local) C0007125 Carcinoma, ehrlich tumor HSDN C4084773 Bothered by weight gain C0042974 Von willebrand disease HSDN C0700078 Deep tendon reflex decrease C2678061 Scapuloperoneal myopathy, x-linked dominant MalaCards|HPO C0023218 Lower extremity cramp C0740728 Lower extremity problem UMLS C4085211 Pain distress question C0034194 Pyloric stenosis HSDN C3815497 Cough C0027932 Neurotic disorders HSDN C0234378 Postural tremor C3149907 Als13 HPO C0151786 Weakness muscle C4084909 Depression subordinate domain HSDN C0018772 Deafness C1546949 Event consequence - death HSDN C2242996 Tingling C0007959 Charcot-marie-tooth disease HSDN C2315100 Pediatric failure to thrive C2749477 Oculodentodigital dysplasia, autosomal recessive MalaCards|HPO C4084775 Usual severity weight loss C0033906 Psychological theories HSDN C1963137 Hydrocephalus adverse event C0406612 Encephalocraniocutaneous lipomatosis MalaCards|HPO C0000737 Abdomen pain C0279661 Acinar cell carcinoma of pancreas UMLS C1963086 Confusion adverse event C0678274 Alcohol abstinence HSDN C0030193 Sense of pain C4054601 Localized adult undifferentiated high grade pleomorphic sarcoma UMLS C0020438 Hypercalciuria C0019202 Hepatolenticular degeneration MalaCards|HSDN|HPO C1961131 Cough adverse event C0040053 Thrombosis HSDN C0026826 High muscle tone C0018802 Congestive heart failure HSDN C1963071 Back pain adverse event C0025202 Melanoma HSDN C0016199 Pain flank C1334602 Malignant mest UMLS C1557397 Adverse event associated with pain C0085222 Psoas muscle abscess HSDN C4084769 Vomiting frequency C1304456 Congo hemorrhagic fever MalaCards C0026858 Musculoskeletal pain C0016510 Foot diseases HSDN C0019209 Large liver C1855467 Macrosomia microphthalmia cleft palate OrphaNet|MalaCards C2242996 Tingling C1556061 Electric injuries HSDN C4084784 Diarrhea C0001618 Tumors of adrenal cortex HSDN C0041834 Erythematous condition C3873472 Vulvovaginal gingival syndrome MalaCards C0236000 Jaw bone pain C0014805 Primary erythermalgia MalaCards|UMLS C0036572 Convulsion C4041299 Intractable partial occipital lobe epilepsy with impairment of consciousness UMLS C4084784 Diarrhea C0878544 Cardiomyopathies HSDN C1963091 Diarrhea adverse event C0004239 Atrial flutter HSDN C0700078 Deep tendon reflex decrease C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C0030193 Sense of pain C0017536 Giardiasis HSDN C3463815 Feel fatigue C0001726 Affective symptoms HSDN C2165508 Depression accompanied by eating less C0011581 Depressive disorder UMLS C2096293 Ent surgical result ear vertigo C0001721 Emotional affect HSDN C0231710 Buttock pain C0740728 Lower extremity problem UMLS C2911647 Weight gain adverse event C0031900 Pierre robin syndrome HSDN C0234512 Prosopagnosia C0338430 Limbic encephalitis HSDN C0206146 Myocardial stunning C0344435 Ventricular fibrillation by ecg finding HSDN C1971624 Appetite absent C0595888 Phosphate serum decreased HSDN C0151786 Weakness muscle C0751891 Hemorrhage, hypertensive intracranial HSDN C0033774 Skin pruritus C0263342 Urticaria pigmentosa, maculopapular type UMLS C1962956 Flatulence adverse event C3489393 Hiatal hernia HSDN C0009806 Constipate C1384606 Dyspareunia HSDN C0406671 Burning scrotum C0037274 Dermatologic disorders UMLS C4085210 Usual severity pain C0007771 Intracranial arteriosclerosis HSDN C0027497 Queasy C0027809 Neurilemmoma HSDN C0278152 Hemifacial spasms C0018920 Hemangioma, cavernous HSDN C0030486 Extremity paralysis, lower C0004935 Animal ethology HSDN C4084726 Distress cough C0023418 Leukemia HSDN C0012833 Dizzy C0206663 Neuroectodermal tumor, primitive MalaCards C0038002 Spleen enlargement C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0557874 Global developmental delay C0795841 Jacobsen distal 11q deletion syndrome OrphaNet|HPO|MalaCards C0018991 Paralysis one side of body C1963137 Hydrocephalus adverse event HSDN C2128230 Loss of skin lines C1862092 Brachydactyly-distal symphalangism syndrome MalaCards C1384666 Decreased hearing C2931888 Pfeiffer type acrocephalosyndactyly MalaCards C4084727 Cough frequency C0162526 Aids-related opportunistic infections HSDN C1549543 Administration method - pain C1302808 Myopericytoma HSDN C2911645 Weight loss adverse event C0085407 Infection by cnidospora, nos HSDN C0003811 Cardiac rhythm disturbance C0010308 Congenital hypothyroidism MalaCards C0003910 Articulation disorder C0039494 Temporomandibular joint disorders HSDN C2203646 Jaundice C0006264 Bronchial neoplasms HSDN C1557397 Adverse event associated with pain C0025060 Mediastinal cyst HSDN C0426579 Anorexia symptom C0238027 Botulism, infantile OrphaNet|MalaCards C0413252 Hypothermia due to exposure C1547046 Kind of quantity - taste HSDN C2919142 Short stature adverse event C3554415 Arthrogryposis, distal, type 5d MalaCards C0000737 Abdomen pain C0854781 Stage i rectosigmoid cancer UMLS C1963237 Insomnia adverse event C0162531 Hereditary coproporphyria HPO C1963087 Constipation adverse event C0702166 Acne HSDN C0518090 Frequency of pain question C0036875 Disorders of sex development HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0003811 Cardiac arrhythmia HSDN C0857305 Thrombocytopenia purpura C0017178 Gastrointestinal diseases HSDN C0007758 Cerebellar ataxia C0033578 Prostatic neoplasms HSDN C1519353 Skin eruption papular C3489795 Hyper-ige recurrent infection syndrome, autosomal dominant OrphaNet|HPO C4084775 Usual severity weight loss C0007194 Hypertrophic cardiomyopathy HSDN C0018772 Deafness C1963090 Dehydration adverse event HSDN C0019079 Bloody sputum C1336215 Stage iiia small cell carcinoma of lung UMLS C4085210 Usual severity pain C0033575 Prostatic diseases HSDN C0015672 Decreased energy C0149678 Epstein-barr virus infections HSDN C4084766 Vomiting C0034531 Experimental radiation injuries HSDN C0003910 Articulation disorder C0030977 Perceptual masking HSDN C1999266 Depression adverse event C0334123 Histiocytosis, lipoid MalaCards C1963093 Dizziness adverse event C1961100 Erectile dysfunction adverse event HSDN C0018991 Paralysis one side of body C0009450 Disease caused by microorganism HSDN C4085222 Nausea C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards C0009676 Confusion state C0033903 Psychologic technic HSDN C4084723 Constipation C0011875 Diabetic angiopathies HSDN C0427055 Face weakness C1850569 Nemaline myopathy 2 HPO|UMLS C2096293 Ent surgical result ear vertigo C0024115 Lung diseases HSDN C2984057 Have nausea C2936636 Anticipation, psychological HSDN C0019825 Voice hoarseness C0031049 Tuberculous pericarditis HSDN C0522224 Palsied C0011630 Dermatomycoses HSDN C0036659 Sensation disorder C0009759 Conjunctival diseases HSDN C0080274 Retention urinary C0432322 Dominant dystrophic epidermolysis bullosa, albopapular type (disorder) HPO C0011991 Loose stools C0008313 Cholangitis, sclerosing UMLS C0018681 Headache, cephalalgia C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0018772 Deafness C0026707 Mucopolysaccharidosis iv OrphaNet|HSDN|MalaCards C2919142 Short stature adverse event C0271742 Glucocorticoid deficiency with achalasia OrphaNet|HPO C0019079 Bloody sputum C0206704 Carcinoma, large cell HSDN C0036572 Convulsion C1299598 Seizures due to metabolic disorder UMLS C2242996 Tingling C0026896 Myasthenia gravis MalaCards C0727671 Red cross toothache drops C0011430 Dentin dysplasia HSDN C1963274 Vasculitis adverse event C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C1384607 Food deprivation HSDN C0002622 Amnesias C0013117 Dreaming HSDN C2237041 Shox gene with short stature C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards C1963252 Tremor adverse event C0032914 Pre-eclampsia HSDN C0030552 Paralysis partial C0342257 Complications of diabetes mellitus HSDN C0033774 Skin pruritus C3813607 Infantile gastroesophageal reflux HSDN C0231341 Aging premature C0004277 Tooth attrition HSDN C0518090 Frequency of pain question C0339289 Injury corneal HSDN C0018524 Hallucinate C0043207 Wolfram syndrome MalaCards|HPO C0151786 Weakness muscle C0019080 Hemorrhage HSDN C0027497 Queasy C1956346 Coronary artery disease HSDN C0026838 Spasticity muscle C0003864 Arthritis HSDN C0349588 Stature short C0406723 Growth retardation, alopecia, pseudoanodontia and optic atrophy OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0037305 Neoplasm, skull HSDN C4084802 Usual severity diarrhea C0041834 Erythema HSDN C1963184 Nystagmus adverse event C0342683 Albinism, oculocutaneous, type iii OrphaNet|HPO|MalaCards C0030554 Abnormal sensation C0016398 Focal infection, dental HSDN C0497406 Over weight C0003431 Antisocial personality disorder HSDN C0018834 Brash C0026272 Mixed connective tissue disease OrphaNet|MalaCards C0030486 Extremity paralysis, lower C0016057 Fibrosarcoma HSDN C0027497 Queasy C0013377 Dysgerminoma HSDN C0034150 Skin purpura C1290398 Cerebral arterial aneurysm HSDN C0039070 Collapse fleeting C0021053 Immune system diseases HSDN C3641755 Have constipation C0025467 Mesentery, cyst HSDN C1549543 Administration method - pain C0020621 Hypokalemia HSDN C2024878 Cardiovascular surgery result: dyspnea C0013928 Fat embolism HSDN C0010200 Cough symptom C0011849 Diabetes mellitus HSDN C0039870 Leanness C0029458 Osteoporosis, postmenopausal HSDN C4085548 Usual severity dizziness C0017181 Gastrointestinal hemorrhage HSDN C0020672 Body temperature decreased C0035435 Rheumatism HSDN C1549543 Administration method - pain C0019562 Von hippel-lindau syndrome HSDN C0015469 Facial paralysis C0014378 Enterovirus infections HSDN C0427055 Face weakness C0011989 Camurati-engelmann syndrome MalaCards|HPO C1963252 Tremor adverse event C0038661 Suicide HSDN C0264611 Apraxia of speech C0268151 Classical galactosemia OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C0041466 Typhoid fever MalaCards|HSDN C0013456 Pain ear C0265761 Congenital laryngocele HSDN C3641756 Have diarrhea C0039730 Thalassemia HSDN C1279888 Proteinuria of undiagnosed cause C0008728 Churg-strauss syndrome MalaCards C0085128 Cardiac output elevated C0023893 Liver cirrhosis, experimental HSDN C3887873 Hearing loss C0024299 Lymphoma HSDN C0427055 Face weakness C1834014 Oculopharyngodistal myopathy MalaCards|UMLS C0042571 Vertigo subjective C0155522 Other labyrinth disorders UMLS C0009806 Constipate C0013502 Echinococcosis HSDN C0043094 Weight gain C0018674 Head trauma HSDN C0022408 Disorder joint C1859405 Bowen-conradi syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0267797 Acute hepatitis UMLS C0018775 Hearing loss bilateral C0022610 Kernicterus HSDN C2127296 Fainting preceded by seeing a mouse C0340849 Fainting simple UMLS C0016382 Cutaneous vascular engorgement C0019625 Sinus histiocytosis MalaCards C4042891 Sleep wake disorders C0024228 Lymphatic diseases HSDN C4042891 Sleep wake disorders C0520680 Sleep apnea, central HSDN C0009398 Color vision defects C0041327 Tuberculosis, pulmonary HSDN C4084766 Vomiting C0346303 Thyrotroph adenoma OrphaNet|MalaCards C0022346 Yellow skin C0008073 Developmental disabilities HSDN C0013404 Respiratory difficulty C0376545 Hematologic neoplasms HSDN C0018808 Murmur C0020725 Type ii mucolipidosis MalaCards|HPO C0011991 Loose stools C0009782 Connective tissue diseases HSDN C0009421 Comatose C0035309 Retinal diseases HSDN C0413252 Hypothermia due to exposure C0034885 Rectal neoplasms HSDN C0151786 Weakness muscle C3539923 Cdisc adas-cog - orientation summary score HSDN C4084767 Bothered by vomiting C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C0041657 Consciousness loss C1090821 Sepsis (invertebrate) HSDN C1963071 Back pain adverse event C0153463 Malig neop oth spec pancreas MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0037859 Spermatocele HSDN C0004134 Dyssynergia C0029294 Orofaciodigital syndromes MalaCards C0042798 Vision dim C1842127 Retinitis pigmentosa 26 MalaCards|HPO C4084776 Weight loss C2931876 Hirschsprung disease 1 MalaCards C0027498 Nausea vomiting C0007095 Carcinoid tumor MalaCards C0151786 Weakness muscle C0027073 Myofascial pain syndromes HSDN C3641756 Have diarrhea C0018081 Gonorrhea HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042384 Vasculitis HSDN C0036572 Convulsion C0021843 Intestinal obstruction HSDN C3641756 Have diarrhea C0014850 Esophageal atresia HSDN C0000737 Abdomen pain C0021071 Immunoproliferative small intestinal disease OrphaNet|HSDN|UMLS|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0585216 Alpha-thalassemia myelodysplasia syndrome OrphaNet|HPO C0013362 Dysarthrias C2750509 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 HPO C0036572 Convulsion C3899671 Childhood cerebellar anaplastic astrocytoma UMLS C0018681 Headache, cephalalgia C0276108 Chlamydia infection psittaci MalaCards C0231528 Muscle pain generalized C0004161 Athletic injuries HSDN C1963164 Lymphopenia adverse event C0272167 Reticular dysgenesis MalaCards|HPO C0042928 Paralysis vocal cord C0027932 Neurotic disorders HSDN C4085222 Nausea C4050613 Anxiety scale (basc-2) HSDN C2024878 Cardiovascular surgery result: dyspnea C0032066 Plague vaccines HSDN C4085211 Pain distress question C0025295 Meningitis, pneumococcal HSDN C0041105 Jaw spasm C1458155 Mammary neoplasms HSDN C0848203 Male pelvic pain C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2919142 Short stature adverse event C3280489 Feingold syndrome 2 MalaCards C0042798 Vision dim C0018522 Hallermann's syndrome OrphaNet|MalaCards C1963274 Vasculitis adverse event C0003873 Rheumatoid arthritis MalaCards C4085317 Diarrhea frequency C0015461 Facial neoplasms HSDN C0020578 Hyperventilate C0032019 Pituitary neoplasms HSDN C4084766 Vomiting C0024692 Mandible fracture HSDN C0011991 Loose stools C0268543 Hyperammonemia, type iii MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0039730 Thalassemia HSDN C2037138 Sudden loss of vision in right half of visual field in right eye C0018979 Hemianopsia UMLS C0018524 Hallucinate C0597109 Nurse's role HSDN C0851578 Disorder sleep C0011882 Diabetic neuropathies HSDN C2919142 Short stature adverse event C1846142 Hoyeraal-hreidarsson syndrome OrphaNet|HPO|MalaCards C0751837 Gait ataxic C0206617 Cardiovirus infections HSDN C0003467 Angst C1855606 Burton syndrome MalaCards C0026858 Musculoskeletal pain C0004275 Attitude health HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0439840 Reflex motion descriptor HSDN C1279888 Proteinuria of undiagnosed cause C0023530 Leukopenia HSDN C0011570 Monopolar depression C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C3539890 Pelvic pain causes awakening at night C0001261 Actinomycosis HSDN C2024878 Cardiovascular surgery result: dyspnea C0206604 Arterivirus infections HSDN C0020580 Decreased sensation C0032587 Polyradiculoneuropathy HSDN C2024878 Cardiovascular surgery result: dyspnea C0024003 Lordosis HSDN C1549543 Administration method - pain C0010678 Cysticercosis HSDN C0013604 Edematous C0398623 Thrombophilia HSDN C0019209 Large liver C1856251 Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i HPO C1963246 Sinus tachycardia adverse event C0406645 Amyopathic dermatomyositis MalaCards C3887873 Hearing loss C1546847 Entity name part type - family HSDN C2203646 Jaundice C0019372 Herpesviridae infections HSDN C0042755 Virilisation C0022735 Klinefelter syndrome HSDN C4085211 Pain distress question C0038002 Splenomegaly HSDN C0150055 Pain chronic C0158322 Calcaneus spur HSDN C3463815 Feel fatigue C0236969 Substance-related disorders HSDN C0011206 Delirium acute C0007137 Squamous cell carcinoma HSDN C3829611 Nausea frequency C0302148 Blood clot HSDN C1549543 Administration method - pain C0001327 Laryngitis acute HSDN C1963071 Back pain adverse event C0013926 Aeroembolism HSDN C3815497 Cough C0042111 Urticaria pigmentosa MalaCards C1963281 Vomiting adverse event C1261128 Progeria-like syndrome MalaCards C0018772 Deafness C0001807 Aggressive behavior HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001206 Acromegaly HSDN C2984058 Have pain C1135957 Narrative HSDN C3641756 Have diarrhea C0017689 Glucagonoma OrphaNet|MalaCards C1963063 Anorexia adverse event C0001418 Adenocarcinoma HSDN C0040460 Dental pain C0453996 Tobacco smoking HSDN C1963064 Anxiety adverse event C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0022638 Ketosis C1829813 Malonic acidemia MalaCards C4049644 Depression C0220704 Shprintzen syndrome MalaCards C0242936 Center pain C0043515 Zollinger-ellison syndrome HSDN C0233794 Memory impaired C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0042111 Urticaria pigmentosa HSDN C1549543 Administration method - pain C1458156 Recurrent malignant neoplasm HSDN C0242936 Center pain C0848558 Hypospadias HSDN C0013428 Painful urination C0041321 Tuberculosis, miliary HSDN C1384666 Decreased hearing C1852278 Deafness-craniofacial syndrome MalaCards C2984058 Have pain C1548484 Rheumatic fever vaccine HSDN C0043094 Weight gain C1136321 Hiv-associated lipodystrophy syndrome HSDN C0030193 Sense of pain C1334439 Adenoid cystic carcinoma of lung UMLS C0423665 Hand joint pain C2702823 Compression arthralgia of right hand UMLS C3641756 Have diarrhea C3150752 Agammaglobulinemia 4, autosomal recessive HPO C0497406 Over weight C0003469 Anxiety disorders HSDN C0018772 Deafness C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0039239 Tachycardia sinus C1866552 Paragangliomas 2 (disorder) MalaCards C1963091 Diarrhea adverse event C0014118 Endocarditis HSDN C4084784 Diarrhea C0032965 Pregnancy complications, infectious HSDN C4084727 Cough frequency C0001807 Aggressive behavior HSDN C0042963 Symptoms vomiting C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C0235153 Sensory hallucination C0043207 Wolfram syndrome MalaCards|HPO C0162298 Stiffness joints C2985290 Fetal alcohol spectrum disorders OrphaNet|MalaCards C2114519 Previously continent child unable to restrain urination C0042024 Urinary incontinence UMLS C0030554 Abnormal sensation C2937358 Cerebral hemorrhage HSDN C1279888 Proteinuria of undiagnosed cause C0042338 Herpesvirus 3, human HSDN C1963237 Insomnia adverse event C0021670 Insulinoma MalaCards|HPO C0030193 Sense of pain C0033348 Language program HSDN C0009806 Constipate C0014858 Esophageal motility disorders HSDN C3539892 Pelvic pain in front C0010356 Cross infection HSDN C0030975 Disorders perception C3811918 Grn-related frontotemporal dementia HSDN C4085210 Usual severity pain C0039483 Giant cell arteritis HSDN C0162834 Hyperpigmentation C0043346 Xeroderma pigmentosum MalaCards C0242936 Center pain C0700345 Candidiasis, vulvovaginal HSDN C4084775 Usual severity weight loss C0000771 Abnormalities, drug induced HSDN C0003862 Pain joint C0015467 Neuralgia facial HSDN C4085210 Usual severity pain C0206711 Pilomatrixoma HSDN C0398650 Idiopathic thrombocytopenia purpura C0023895 Liver diseases HSDN C3146279 Coma C0205788 Histiocytoid hemangioma HSDN C0007758 Cerebellar ataxia C0520719 Spinopontine atrophy MalaCards C3539023 Pelvic pain increasing in frequency C0009373 Colonic diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0020580 Decreased sensation C0015379 Extravasation of diagnostic and therapeutic materials HSDN C4084774 Have weight loss C1261473 Sarcoma HSDN C0034933 Abnormal reflexes C0039223 Tabes dorsalis HSDN C4085210 Usual severity pain C0161406 Injury nerve trigeminal HSDN C0684343 Pseudophakia C0022073 Iridocyclitis HSDN C0040822 D tremors C1623041 Breast-fed HSDN C2315100 Pediatric failure to thrive C1855772 Absent corpus callosum cataract immunodeficiency MalaCards|HPO C0231528 Muscle pain generalized C1969443 Trifunctional protein deficiency with myopathy and neuropathy HPO|UMLS C0020615 Hypoglycemia nos C1837475 Insulin-like growth factor i deficiency MalaCards|HPO C2029884 Hearing loss by exam C0025958 Microcephaly HSDN C0009806 Constipate C0268579 Propionic acidemia OrphaNet|HPO C1963086 Confusion adverse event C0027927 Neurosyphilis HSDN C0026821 Cramp C0033054 Prenatal exposure delayed effects HSDN C4084774 Have weight loss C0595812 Fistula route HSDN C0587047 Mass of trunk C0340241 Infected bronchogenic cyst UMLS C0019209 Large liver C4045991 Perihilar cholangiocarcinoma MalaCards C0013404 Respiratory difficulty C1962979 Burn adverse event HSDN C0277959 Hair coarseness C1843042 Craniolenticulosutural dysplasia OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0013922 Embolism HSDN C2242996 Tingling C3810814 Myocardial infarction ecg assessment HSDN C4084774 Have weight loss C0206644 Histiocytoma, benign fibrous HSDN C0424755 Fever symptoms C0036329 Schistosomiasis japonica DiseaseOntology C1961131 Cough adverse event C1720777 Functional laterality HSDN C3146279 Coma C0517555 Venous thrombosis after immobility HSDN C0042024 Urine incontinence C0517555 Venous thrombosis after immobility HSDN C1963086 Confusion adverse event C0751739 Basal ganglia cerebrovascular disease HSDN C4085661 Usual severity nausea C0021400 Influenza HSDN C0030193 Sense of pain C0022374 Jejunal neoplasms HSDN C0010200 Cough symptom C0018800 Cardiomegaly HSDN C0003126 Smell loss C3553843 Hypogonadotropic hypogonadism 10 with or without anosmia MalaCards C2032396 Pelvic pain on the right C0282606 Myomatous neoplasm HSDN C4084784 Diarrhea C0014118 Endocarditis HSDN C0557874 Global developmental delay C0796126 Aicardi-goutieres syndrome 1 MalaCards|HPO C3274924 Have been coughing C3809651 Infantile liver failure syndrome 2 MalaCards C0028961 Urine output decreased C0034040 Puerperal disorders HSDN C0011991 Loose stools C0017661 Iga glomerulonephritis HSDN C0036659 Sensation disorder C1546533 Specimen source codes - abscess HSDN C1963180 Neck pain adverse event C3714514 Infection HSDN C4085548 Usual severity dizziness C1836438 Familial neurocardiogenic syncope MalaCards C0020673 Hypothermia (central) (local) C0796147 Acrocallosal syndrome HSDN C3898969 Have been vomiting C1862892 Hereditary angioedema type ii HPO C0018772 Deafness C0034531 Experimental radiation injuries HSDN C0020505 Excessive eating C0009244 Behavioral cognitive therapy HSDN C1963281 Vomiting adverse event C0037313 Sleep HSDN C0019825 Voice hoarseness C0031345 Pharyngeal diseases HSDN C0018772 Deafness C1861391 Symphalangism with multiple anomalies of hands and feet MalaCards C4084768 Usual severity vomiting C0001118 Acid base imbalance HSDN C1963071 Back pain adverse event C0027643 Neoplasm recurrence, local HSDN C0036572 Convulsion C2931840 Aspartylglucosamidase (aga) deficiency MalaCards|HPO C0028738 Nystagmus C0265338 Coffin-siris syndrome OrphaNet|HPO C3815497 Cough C0279626 Squamous cell carcinoma of esophagus OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0005398 Cholestasis, extrahepatic HSDN C0003811 Cardiac rhythm disturbance C2717876 Aciduria, propionic OrphaNet|HPO C0030200 Intractable pain C0014859 Esophageal neoplasms HSDN C0035229 Respiratory function impaired C3275954 Lacht MalaCards C4085211 Pain distress question C0019156 Hepatic veno-occlusive disease HSDN C0018681 Headache, cephalalgia C2827407 Infectious otitis media HSDN C4084766 Vomiting C0011303 Demyelinating diseases HSDN C4085222 Nausea C1704326 Role - roleclass HSDN C0242936 Center pain C0042162 Uveal neoplasms HSDN C1963093 Dizziness adverse event C0007789 Cerebral palsy HSDN C0162298 Stiffness joints C1856095 Complex congenital heart defect, renal agenesis, and cleft lip and palate OrphaNet|MalaCards C3539896 Pelvic pain occurs with urination C0001624 Adrenal gland neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C4041080 Neurocognitive disorders HSDN C4084767 Bothered by vomiting C0019569 Hirschsprung disease MalaCards|HSDN C0010200 Cough symptom C1401747 Quadrilateral fever MalaCards C0022408 Disorder joint C0002066 Alkaptonuria MalaCards|HPO C0018772 Deafness C2239351 Deafness, autosomal recessive 74 MalaCards|HPO C0013404 Respiratory difficulty C0027819 Neuroblastoma HSDN C3887873 Hearing loss C0004275 Attitude health HSDN C0007758 Cerebellar ataxia C1847114 Spinocerebellar ataxia, autosomal recessive 5 OrphaNet|HPO C2911645 Weight loss adverse event C0037313 Sleep HSDN C4084767 Bothered by vomiting C0024535 Malaria, falciparum HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027030 Maggot infection HSDN C0231218 Malaise generalized C0041296 Tuberculosis UMLS C0043068 Friderichsen-waterhouse syndrome C0031111 Periostitis HSDN C0031911 Pigment deposition C1299247 Primary malignant neoplasm of ovary and other uterine adnexa MalaCards C4084773 Bothered by weight gain C3489393 Hiatal hernia HSDN C1850830 Exercise-induced muscle pain C0270968 Limb-girdle muscular dystrophy type 2h MalaCards|HPO|UMLS C0150055 Pain chronic C0042830 Perception visual HSDN C0007758 Cerebellar ataxia C1970827 Phosphoribosylpyrophosphate synthetase superactivity MalaCards|HPO C1963071 Back pain adverse event C0024117 Chronic obstructive airway disease HSDN C4084768 Usual severity vomiting C0033845 Pseudotumor cerebri HSDN C0009421 Comatose C0034531 Experimental radiation injuries HSDN C1557397 Adverse event associated with pain C0025205 Melanoma, experimental HSDN C0015970 Fever unknown origin C0085426 Gram-positive bacterial infections HSDN C0029163 Hemorrhage mouth C0014544 Epilepsy HSDN C0023380 Lethargy C0268540 Hhh syndrome HPO|UMLS C1000483 Genus anemia C0002875 Cooley's anemia OrphaNet C3898969 Have been vomiting C1579931 Depressed - symptom HSDN C0010200 Cough symptom C1336125 Stage ia squamous cell carcinoma of lung UMLS C3815497 Cough C0026771 Trauma multiple HSDN C0013404 Respiratory difficulty C0006114 Cerebral edema HSDN C0037763 Spasm C1962986 Glaucoma adverse event HSDN C1279888 Proteinuria of undiagnosed cause C2963140 Arteriovenous fistula in use with two needles HSDN C0042024 Urine incontinence C2750784 Spastic paraplegia 44, autosomal recessive (disorder) MalaCards|HPO C0085128 Cardiac output elevated C0042850 Vitamin b deficiency HSDN C0030552 Paralysis partial C1856403 Etfb deficiencies HPO C0011991 Loose stools C1844663 Islets of langerhans, absence of HPO C0742289 Chest pain char not typical angina C0741025 Chest problem UMLS C0019825 Voice hoarseness C0281890 Laryngeal web OrphaNet|MalaCards C0085631 Abnormal excitement C1838570 Ceroid lipofuscinosis, neuronal, 8 MalaCards C1579931 Depressed - symptom C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C4084769 Vomiting frequency C0019522 Adenoma, sweat gland HSDN C4084776 Weight loss C0019154 Hepatic vein thrombosis MalaCards|HPO C3665386 Abnormal vision C3280011 Brittle cornea syndrome 2 MalaCards C4085317 Diarrhea frequency C1366464 F9 gene HSDN C1384666 Decreased hearing C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C2024878 Cardiovascular surgery result: dyspnea C0028796 Dermatitis, occupational HSDN C0024032 Birth weight subnormal C3809272 Lethal congenital contracture syndrome 5 MalaCards C4084784 Diarrhea C0008519 Ectopic tissue HSDN C0035229 Respiratory function impaired C3714932 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 MalaCards C0018991 Paralysis one side of body C1845050 Pigmentary disorder, reticulate, with systemic manifestations HPO C0041657 Consciousness loss C0009946 Conversion disorder HSDN C0013362 Dysarthrias C0268525 5-oxoprolinase deficiency MalaCards C0018784 Deafness sensorineural C0023138 Laurence-moon syndrome OrphaNet|HPO|MalaCards C1962972 Proteinuria adverse event C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards|HPO C0518090 Frequency of pain question C0032371 Poliomyelitis HSDN C0004310 Auditory disorder process C0032787 Postoperative complications HSDN C2126961 Double vision in one eye when wearing glasses C0271190 Diplopia, unilateral UMLS C0002622 Amnesias C0041755 Adverse reaction to drug HSDN C0600142 Flash hot C0001721 Emotional affect HSDN C1549543 Administration method - pain C0085207 Gestational diabetes HSDN C3146279 Coma C3163620 Hypotension adverse event HSDN C1384666 Decreased hearing C0517555 Venous thrombosis after immobility HSDN C4084767 Bothered by vomiting C0376547 Aromatherapy HSDN C0038002 Spleen enlargement C1858723 Poikiloderma with neutropenia MalaCards|HPO C0917816 Deficiency mental C0795974 Hereditary macular epidermolysis bullosa OrphaNet C0030193 Sense of pain C0015404 Eye infections, bacterial HSDN C0036659 Sensation disorder C0023903 Liver neoplasms HSDN C1557397 Adverse event associated with pain C0040411 Tongue neoplasms HSDN C1069915 Vertigo C3279664 Emberger syndrome MalaCards C0518090 Frequency of pain question C0004626 Pneumonia, bacterial HSDN C0917816 Deficiency mental C0220681 Goldenhar syndrome with ipsilateral radial defect MalaCards C0007758 Cerebellar ataxia C1291609 Ribose 5-phosphate isomerase deficiency MalaCards|HPO|UMLS C0027796 Neuralgias C0018794 Heart block HSDN C0151889 Reflexes tendon increased C3280538 Mental retardation, autosomal recessive 27 MalaCards C2132198 Abnormal blistering of the skin C0032827 Potassium deficiency MalaCards C1963180 Neck pain adverse event C0011265 Presenile dementia HSDN C0030552 Paralysis partial C3469606 Pseudohypoaldosteronism, type iie MalaCards C0036572 Convulsion C0085435 Arthritis, reactive HSDN C2919142 Short stature adverse event C1855606 Burton syndrome MalaCards C1384666 Decreased hearing C0032019 Pituitary neoplasms HSDN C0019079 Bloody sputum C0751674 Lymphangioleiomyomatosis MalaCards|HPO C0424755 Fever symptoms C0013080 Down syndrome HSDN C0242936 Center pain C0023885 Liver abscess HSDN C2145411 Transient monoplegia of left lower extremity C0154702 Paralysis of lower limb UMLS C2237041 Shox gene with short stature C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C0022346 Yellow skin C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0917816 Deficiency mental C0024776 Maple syrup urine disease OrphaNet|HPO C0009806 Constipate C0311298 Propionic acidemia, type ii OrphaNet|HPO C4084769 Vomiting frequency C0013010 Cerebral lateralization HSDN C0020578 Hyperventilate C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0042024 Urine incontinence C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0036572 Convulsion C2931282 Skeletal dysplasia, san diego type MalaCards|HPO C0151889 Reflexes tendon increased C1849128 Spastic paraplegia 15, autosomal recessive MalaCards C0011168 Disorder deglutition C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C0575081 Abnormal gait C0265311 Leri pleonosteosis syndrome MalaCards C0009398 Color vision defects C0022116 Ischemia HSDN C4085211 Pain distress question C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0037763 Spasm C1556682 Adverse event associated with infection HSDN C0033377 Caudal displacement C0221060 Mobius syndrome OrphaNet|HPO|MalaCards C0004604 Pain back C1963083 Cholecystitis adverse event HSDN C1145670 Failure respiratory C1275808 Congenital central hypoventilation OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C4084776 Weight loss C3163620 Hypotension adverse event HSDN C3641755 Have constipation C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0000737 Abdomen pain C0280725 Adult primary cholangiocellular carcinoma UMLS C0000737 Abdomen pain C0010481 Cushing syndrome MalaCards|HSDN|HPO C0019079 Bloody sputum C0023903 Liver neoplasms HSDN C0028738 Nystagmus C2676766 Osteopetrosis, autosomal recessive 7 MalaCards|HPO C0018784 Deafness sensorineural C1846922 Deafness, autosomal dominant 21 (disorder) MalaCards C0030193 Sense of pain C0036349 Paranoid schizophrenia HSDN C1963063 Anorexia adverse event C0153452 Malignant neoplasm of gallbladder OrphaNet C0018784 Deafness sensorineural C3553937 Pbd4b MalaCards C4085317 Diarrhea frequency C0025517 Metabolic diseases HSDN C0034155 Thrombotic thrombocytopenic purpura C1458155 Mammary neoplasms HSDN C0004604 Pain back C0750221 Vertebra disc herniation UMLS C0020455 Hypergammaglobulinemia C2984289 Melanoma pathway HSDN C0151798 Liver necrosis C0025517 Metabolic diseases MalaCards C1557397 Adverse event associated with pain C0014534 Epididymitis HSDN C0010200 Cough symptom C0036341 Schizophrenia HSDN C2984058 Have pain C0018552 Hamartoma HSDN C2911645 Weight loss adverse event C0002792 Anaphylaxis HSDN C0028738 Nystagmus C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0013404 Respiratory difficulty C0013182 Drug allergy HSDN C4084768 Usual severity vomiting C0162576 Anisakiasis HSDN C0018808 Murmur C0010674 Cystic fibrosis HSDN C0454644 Delayed language development C1850985 Fragile site 16p12 HPO C0007758 Cerebellar ataxia C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO C0948396 Frequent headache C0010273 Craniofacial dysostosis MalaCards C1963086 Confusion adverse event C1527311 Brain edema HSDN C2881387 Visual discomfort, left eye C0809996 Blindness and vision defects UMLS C2984058 Have pain C0041955 Ureteral neoplasms HSDN C4085211 Pain distress question C0027661 Neoplasms, hormone-dependent HSDN C0008031 Pain chest C1290398 Cerebral arterial aneurysm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0079731 B-cell lymphomas HSDN C0424810 Periorbital swelling C0406645 Amyopathic dermatomyositis MalaCards C0026838 Spasticity muscle C1845862 Creatine deficiency, x-linked MalaCards|HPO|UMLS C0242936 Center pain C0029132 Disorder of the optic nerve HSDN C4085862 Bothered by nausea C0270858 Abdominal migraines MalaCards C0003910 Articulation disorder C0079173 Craniomandibular disorders HSDN C0021359 Infertility C0008043 Chiari-frommel syndrome MalaCards C4084723 Constipation C1963137 Hydrocephalus adverse event HSDN C1963093 Dizziness adverse event C0264903 Premature ventricular complex multifocal MalaCards C0002622 Amnesias C0036864 Sexual relations HSDN C0750394 Wbc low C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C0020615 Hypoglycemia nos C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0018772 Deafness C0023473 Myeloid leukemia, chronic HSDN C2984058 Have pain C0037199 Sinusitis HSDN C3274924 Have been coughing C0035435 Rheumatism HSDN C0086437 Joint hypermobility C0175702 Williams syndrome MalaCards|HPO|UMLS C0424755 Fever symptoms C0022423 Judgement HSDN C1963281 Vomiting adverse event C0205770 Choroid plexus papilloma HSDN|HPO C0004604 Pain back C0020550 Hyperthyroidism HSDN C0151908 Dry skin C0265961 Erythrokeratodermia variabilis OrphaNet|HPO C0003862 Pain joint C1963274 Vasculitis adverse event HSDN C0007758 Cerebellar ataxia C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0004093 Asthenia C0020524 Disorders of excessive somnolence HSDN C0027066 Myoclonic jerking C0016169 Pathologic fistula HSDN C0000727 Abdomen acute C0030922 Peptic ulcer hemorrhage HSDN C0013421 Dystonia C1258104 Diffuse scleroderma HSDN C0018524 Hallucinate C0030783 Pellagra HSDN C0232466 Feeding difficulty C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0007453 Cattle disease HSDN C0026838 Spasticity muscle C0795822 8 rec syndrome OrphaNet|MalaCards C4084802 Usual severity diarrhea C1548777 Specimen reject reason - hemolysis HSDN C0042024 Urine incontinence C0018674 Head trauma HSDN C0018681 Headache, cephalalgia C3647009 Periodic headache syndromes with intractable migraine UMLS C0042963 Symptoms vomiting C1963059 Adrenal insufficiency adverse event HSDN C2237041 Shox gene with short stature C0086651 Mucopolysaccharidosis, mps-iv-a OrphaNet|MalaCards C3887873 Hearing loss C0015393 Eye abnormalities HSDN C2242996 Tingling C0038994 Gustatory sweating HSDN C4085211 Pain distress question C0016045 Fibroma HSDN C2919142 Short stature adverse event C1850040 Pelviscapular dysplasia OrphaNet|HPO|MalaCards C2984057 Have nausea C0007527 Cecal disease HSDN C0042963 Symptoms vomiting C0004933 Behavior modification technique HSDN C0042025 Urinary incontinence stress C1704212 Embolism embolus HSDN C0011175 Deficient fluid volume C1832386 Diabetes mellitus, transient neonatal, 1 OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0023440 Acute erythroblastic leukemia HSDN C0563661 Hallucination, reflex C0018524 Hallucinations UMLS C0518090 Frequency of pain question C0034186 Pyelonephritis HSDN C0036572 Convulsion C0078982 Arhinencephaly MalaCards C0036659 Sensation disorder C0027868 Neuromuscular diseases HSDN C4084775 Usual severity weight loss C1998602 Meals HSDN C0042024 Urine incontinence C1134719 Invasive ductal breast carcinoma HSDN C0036572 Convulsion C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C1963065 Apnea adverse event C0000833 Abscess HSDN C0003910 Articulation disorder C0003873 Rheumatoid arthritis HSDN C3641756 Have diarrhea C0024282 Lymphocytosis HSDN C1961131 Cough adverse event C2984572 Malaria pathway HSDN C4085210 Usual severity pain C0001623 Adrenal gland hypofunction HSDN C4084784 Diarrhea C0236736 Cocaine-related disorders HSDN C0020672 Body temperature decreased C1263846 Attention deficit hyperactivity disorder HSDN C0009676 Confusion state C1527311 Brain edema HSDN C2919142 Short stature adverse event C0282529 Chondrodysplasia punctata, rhizomelic OrphaNet|MalaCards C0085631 Abnormal excitement C0997768 Glaucoma HSDN C0424755 Fever symptoms C0702221 Tactual discrimination HSDN C1384666 Decreased hearing C3152102 Ush1d/f, cdh23/pcdh15, digenic HPO C4084802 Usual severity diarrhea C0020473 Hyperlipidemia HSDN C1279888 Proteinuria of undiagnosed cause C1704436 Peripheral arterial diseases HSDN C1963086 Confusion adverse event C0023903 Liver neoplasms HSDN C0018926 Emesis bloody C0039445 Hereditary hemorrhagic telangiectasia HPO C0018991 Paralysis one side of body C1546847 Entity name part type - family HSDN C0020672 Body temperature decreased C0014072 Experimental autoimmune encephalomyelitis HSDN C2984058 Have pain C3146297 Study of behavior during childhood HSDN C0036572 Convulsion C0314657 Genetic predisposition HSDN C0027796 Neuralgias C0036864 Sexual relations HSDN C0009792 Consciousness disorder C0033975 Psychotic disorders HSDN C1963184 Nystagmus adverse event C0342777 Succinate-coenzyme q reductase deficiency MalaCards C0030193 Sense of pain C0265706 Gastroschisis HSDN C4084774 Have weight loss C1881674 Medical device emits smoke HSDN C3887873 Hearing loss C3536983 Familial hypophosphatemic rickets HSDN C4085317 Diarrhea frequency C3469186 Hemochromatosis, type 1 HSDN C3887873 Hearing loss C0005591 Avian disease HSDN C1961131 Cough adverse event C0001144 Acne vulgaris HSDN C0242936 Center pain C1504665 Products used to treat diabetic ketoacidosis HSDN C1290771 Edema of oral vestibule C1290849 Disorder characterised by oedema UMLS C4084773 Bothered by weight gain C0028432 Nose diseases HSDN C0020578 Hyperventilate C0037744 Perceptual spatial orientation HSDN C1279888 Proteinuria of undiagnosed cause C3163620 Hypotension adverse event HSDN C0030552 Paralysis partial C0282492 Sneddon syndrome OrphaNet|HPO|MalaCards C0009398 Color vision defects C0011265 Presenile dementia HSDN C1000483 Genus anemia C3468041 Fanconi anemia, complementation group c MalaCards C2096293 Ent surgical result ear vertigo C1134719 Invasive ductal breast carcinoma HSDN C0518090 Frequency of pain question C1258215 Ileus HSDN C0030486 Extremity paralysis, lower C0018273 Growth disorders HSDN C0026838 Spasticity muscle C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C0015970 Fever unknown origin C0020538 Hypertensive disease HSDN C3539023 Pelvic pain increasing in frequency C0023467 Leukemia, myelocytic, acute HSDN C4084774 Have weight loss C0152018 Esophageal carcinoma OrphaNet|MalaCards C0085602 Polydypsia C0042075 Urologic diseases MalaCards C4085211 Pain distress question C0009021 Clonorchiasis HSDN C4085661 Usual severity nausea C1999266 Depression adverse event HSDN C0036572 Convulsion C0039538 Teratoma HSDN C0700590 Diaphoresis excessive C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C0004134 Dyssynergia C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0018772 Deafness C0282102 Chondrodysplasia punctata, x-linked dominant type HPO C0522224 Palsied C0020488 Hypernatremia HSDN C1963249 Tinnitus adverse event C0041327 Tuberculosis, pulmonary HSDN C0086565 Liver function abnormal C1849678 Peroxisomal acyl-coa oxidase deficiency MalaCards|HPO C0401149 Constipation chronic C1862936 Anal sphincter dysplasia MalaCards C0011206 Delirium acute C2937421 Prostatic hyperplasia HSDN C1963281 Vomiting adverse event C4012395 Congenital disorder of glycosylation, type iy MalaCards C4085211 Pain distress question C0005745 Blepharoptosis HSDN C3541349 Syncope C0030305 Pancreatitis HSDN C0012569 Double vision C0018671 Head and neck neoplasms HSDN C1549543 Administration method - pain C0036472 Scrub typhus HSDN C0242936 Center pain C0747533 Peroneal neuropathy HSDN C0003862 Pain joint C0024445 Lipomatosis, familial benign cervical OrphaNet|HPO|MalaCards C0008031 Pain chest C0279628 Adenocarcinoma of esophagus OrphaNet C3463815 Feel fatigue C2239176 Liver carcinoma MalaCards|HSDN C0011991 Loose stools C0011848 Diabetes insipidus HSDN C0013604 Edematous C0038220 Status epilepticus HSDN C0030554 Abnormal sensation C0270611 Brain damage HSDN C1557397 Adverse event associated with pain C0035042 Psychology and religion HSDN C0019209 Large liver C2873856 Essential cryoglobulinemia MalaCards C0019825 Voice hoarseness C0016658 Fracture bone HSDN C4084763 Frequency of shortness of breath C0149514 Bronchitis acute DiseaseOntology|MalaCards C0151786 Weakness muscle C1846170 Mental retardation, x-linked, syndromic 7 OrphaNet|MalaCards C0036572 Convulsion C0043395 Yellow fever HSDN C1963071 Back pain adverse event C1963178 Myelitis adverse event HSDN C1557397 Adverse event associated with pain C0016665 Fracture, nos with nonunion HSDN C0026838 Spasticity muscle C0004045 Asphyxia neonatorum HSDN C0013456 Pain ear C0006105 Brain abscess HSDN C1549543 Administration method - pain C0035078 Kidney failure HSDN C0040264 Ear ringing sound C0011860 Diabetes mellitus, non-insulin-dependent HSDN C1279888 Proteinuria of undiagnosed cause C2350521 Gustatory perception HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007786 Brain ischemia HSDN C0043094 Weight gain C2937287 Hematolysis HSDN C2242577 Oromandibular dystonia C1843264 Dystonia 13, torsion MalaCards C0018834 Brash C3810814 Myocardial infarction ecg assessment HSDN C0242936 Center pain C0023485 Precursor b-cell lymphoblastic leukemia-lymphoma HSDN C1963252 Tremor adverse event C2984291 Glioblastoma multiforme pathway HSDN C0009398 Color vision defects C0037274 Dermatologic disorders HSDN C2032395 Pelvic pain on the left C0023903 Liver neoplasms HSDN C0030486 Extremity paralysis, lower C0035242 Respiratory tract diseases HSDN C4084784 Diarrhea C0015726 Focused anxiety HSDN C0010200 Cough symptom C0025521 Inborn errors of metabolism HSDN C3541349 Syncope C0039614 Tetanus HSDN C0013390 Cramps menstrual C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0042928 Paralysis vocal cord C0020732 Iatrogenic disease HSDN C0018681 Headache, cephalalgia C0019099 Hemorrhagic fever, crimean DiseaseOntology|OrphaNet|MalaCards C1963071 Back pain adverse event C0162316 Iron deficiency anemia HSDN C4085210 Usual severity pain C0040425 Tonsillitis HSDN C0016199 Pain flank C0019326 Ventral hernia HSDN C0041657 Consciousness loss C0403459 Traumatic anuria - crush syndrome HSDN C0242936 Center pain C0497572 Female genital herpes HSDN C0026838 Spasticity muscle C0042769 Virus diseases HSDN C0040822 D tremors C1860860 Neuhauser daly magnelli syndrome MalaCards C2203646 Jaundice C0220991 Rotor syndrome OrphaNet|HPO C0030486 Extremity paralysis, lower C0206245 Amyloid neuropathies, familial MalaCards C0018784 Deafness sensorineural C2677903 Mental retardation and microcephaly with pontine and cerebellar hypoplasia OrphaNet|HPO|MalaCards C0576456 Poor feeding C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards C1971624 Appetite absent C0012644 Animal disease models HSDN C3887873 Hearing loss C0001193 Apert syndrome MalaCards|HSDN C1557397 Adverse event associated with pain C0596263 Carcinogenesis HSDN C1856661 Cornea cloudy C1704429 Hypoalphalipoproteinemia, familial MalaCards C4084768 Usual severity vomiting C0008065 Childhood behavior HSDN C0036572 Convulsion C0221021 Microangiopathic hemolytic anemia MalaCards C0009398 Color vision defects C0014544 Epilepsy HSDN C0009398 Color vision defects C0042830 Perception visual HSDN C0086565 Liver function abnormal C2931007 Congenital disorder of glycosylation type 1x MalaCards C0151889 Reflexes tendon increased C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards C0241137 Skin pallor C0041834 Erythema HSDN C0022346 Yellow skin C0038579 Substance abuse, intravenous HSDN C3665347 Vision impaired C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards|HPO C0231791 In toe C0265226 Hecht syndrome (disorder) HPO C3665347 Vision impaired C1864877 Csnb, incomplete, autosomal recessive MalaCards|HPO C0011570 Monopolar depression C0162671 Melas syndrome OrphaNet|HPO|MalaCards C1963063 Anorexia adverse event C0036864 Sexual relations HSDN C0011991 Loose stools C1579830 Cutaneous vesicle HSDN C0030552 Paralysis partial C0007873 Uterine cervical neoplasm HSDN C0018772 Deafness C0220756 Niemann-pick disease, type c HSDN C0015672 Decreased energy C0751552 Malignant neoplasm of thymus MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0877149 Pain patellofemoral syndrome HSDN C0037763 Spasm C0919267 Ovarian neoplasm HSDN C0426579 Anorexia symptom C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C0010200 Cough symptom C0742746 Congestive heart failure decompensated UMLS C0031315 Phantom limb pain C0013808 Electroconvulsive therapy HSDN C2237041 Shox gene with short stature C1449844 Pseudohypoaldosteronism, type ii MalaCards C1959630 Eye pain adverse event C0038379 Eye deviation HSDN C0010200 Cough symptom C0746158 Lung lll pneumonia UMLS C1549543 Administration method - pain C0017919 Glycogen storage disease HSDN C3641756 Have diarrhea C0872996 Q fever vaccine HSDN C2984058 Have pain C0032994 Pregnancy, tubal HSDN C0242936 Center pain C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C0349489 Fetal hypoxia C0037286 Skin neoplasms HSDN C0019079 Bloody sputum C0014118 Endocarditis HSDN C4084788 Have dizziness C3554047 Ventricular tachycardia, catecholaminergic polymorphic, 4 MalaCards C1557397 Adverse event associated with pain C0853986 Lymphocytes decreased HSDN C4084726 Distress cough C2117118 X-ray of toe: deformity contracture HSDN C3541349 Syncope C0008626 Congenital chromosomal disease HSDN C0020455 Hypergammaglobulinemia C0032962 Pregnancy complications HSDN C3463815 Feel fatigue C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C4084768 Usual severity vomiting C0270858 Abdominal migraines MalaCards C0019209 Large liver C0175683 Citrullinemia HPO C4084768 Usual severity vomiting C0017181 Gastrointestinal hemorrhage HSDN C1963249 Tinnitus adverse event C0221759 Brachial plexus neuritis HSDN C1963281 Vomiting adverse event C0009240 Cognition HSDN C3539891 Pelvic pain to the rear C1550672 Specimen type - ulcer HSDN C0030552 Paralysis partial C0037019 Shy-drager syndrome HSDN C0231218 Malaise generalized C0032285 Pneumonia UMLS C0035078 Failure kidney C0017924 Glycogen storage disease type v HPO C0007758 Cerebellar ataxia C0013533 Echovirus infections HSDN C4084725 Usual severity cough C0206628 Mesoblastic nephroma HSDN C0020615 Hypoglycemia nos C1858656 Short stature, idiopathic, autosomal MalaCards C1963252 Tremor adverse event C0040156 Thyrotoxicosis HSDN C0085128 Cardiac output elevated C0238096 Embolism, paradoxical HSDN C4042891 Sleep wake disorders C0027902 Neuropsychological diagnosis HSDN C0476273 Distress respiratory C1956258 Familial thrombotic thrombocytopenic purpura HPO C0007758 Cerebellar ataxia C1850597 Leigh syndrome due to mitochondrial complex ii deficiency HPO C1557397 Adverse event associated with pain C0041328 Renal tuberculosis HSDN C4085222 Nausea C0019348 Herpes simplex infections HSDN C0026838 Spasticity muscle C0013182 Drug allergy HSDN C0013395 Indigestion C0040034 Thrombocytopenia HSDN C0000737 Abdomen pain C3897124 Bclc stage a hepatocellular carcinoma UMLS C0002962 Angina C0014118 Endocarditis HSDN C1963167 Memory impairment adverse event C1333990 Hereditary nonpolyposis colorectal cancer MalaCards|HPO C2096293 Ent surgical result ear vertigo C0017563 Gingival diseases HSDN C0033774 Skin pruritus C0795969 Cholestasis-pigmentary retinopathy-cleft palate syndrome MalaCards C3829611 Nausea frequency C0042826 Field visual HSDN C1963252 Tremor adverse event C0162671 Melas syndrome MalaCards|HPO C0018784 Deafness sensorineural C0243026 Sepsis HSDN C4042891 Sleep wake disorders C0563150 Catastrophization HSDN C0398650 Idiopathic thrombocytopenia purpura C2936664 Acquired hypogammaglobulinemia MalaCards C0349588 Stature short C0410180 Eichsfeld type congenital muscular dystrophy HPO C0349588 Stature short C1851413 Exostoses, multiple, type ii HPO C0043094 Weight gain C0019069 Hemophilia a HSDN C1999266 Depression adverse event C0001206 Acromegaly OrphaNet|HPO|MalaCards C0015468 Face pain C1546847 Entity name part type - family HSDN C2096293 Ent surgical result ear vertigo C0007131 Non-small cell lung carcinoma HSDN C4085642 Level of joint stiffness C1527406 Rhizomelic pseudopolyarthritis MalaCards C0239779 Grimacing C0026650 Movement disorders UMLS C0838227 Pain in a joint, lower leg C0810055 Other non-traumatic joint disorders UMLS C0041834 Erythematous condition C0086768 Pancreatic cholera OrphaNet|MalaCards C0085636 Light sensitivity C4014676 Ataxia-telangiectasia-like disorder 2 UMLS C4084784 Diarrhea C0042487 Venous thrombosis HSDN C0012569 Double vision C0043019 Lateral medullary syndrome HSDN C0020672 Body temperature decreased C1269683 Major depressive disorder HSDN C0018965 Blood urine C0086922 Purpura rheumatoid OrphaNet|MalaCards C1961131 Cough adverse event C0004576 Babesiosis OrphaNet|MalaCards C0004134 Dyssynergia C0270858 Abdominal migraines MalaCards C2129513 Midback pain worse with driving over rough terrain C1861835 Cataract, aberrant oral frenula, and growth retardation MalaCards C0034155 Thrombotic thrombocytopenic purpura C1963274 Vasculitis adverse event HSDN C0019079 Bloody sputum C0524799 Hyperlucent lung HSDN C0151786 Weakness muscle C0027873 Neuromyelitis optica HSDN C4084766 Vomiting C0341106 Eosinophilic esophagitis MalaCards|HSDN C0042798 Vision dim C0004364 Autoimmune diseases HSDN C0231341 Aging premature C0270972 Cornelia de lange syndrome HSDN C1000483 Genus anemia C2931082 Familial apoceruloplasmin deficiency MalaCards C4085211 Pain distress question C0162532 Variegate porphyria MalaCards C1860844 Sparse, thin hair C1148551 X-linked dyskeratosis congenita MalaCards C4084774 Have weight loss C0037939 Spinal neoplasms HSDN C0018681 Headache, cephalalgia C0206754 Neuroendocrine tumors HSDN C0002965 Crescendo angina C3813607 Infantile gastroesophageal reflux HSDN C0018772 Deafness C1509147 Histiocytoma HSDN C0278115 Paraplegic spinal paralysis C0037928 Spinal cord diseases UMLS C0002624 Amnesia retrograde C0037744 Perceptual spatial orientation HSDN C2203646 Jaundice C0021841 Intestinal neoplasms HSDN C0015672 Decreased energy C2242987 Benign mastocytoma MalaCards C0013395 Indigestion C4042784 Feeding and eating disorders HSDN C0036572 Convulsion C2678051 Mental retardation, x-linked 94 (disorder) MalaCards|HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0030499 Parasitic diseases HSDN C0043352 Absent salivary secretion C1866983 Scleroderma, familial progressive MalaCards C2237041 Shox gene with short stature C1859252 Cerebrofaciothoracic dysplasia OrphaNet|HPO|MalaCards C1519353 Skin eruption papular C0008728 Churg-strauss syndrome MalaCards C0018926 Emesis bloody C0011880 Diabetic ketoacidosis HSDN C0013421 Dystonia C0002949 Aneurysm, dissecting HSDN C0004604 Pain back C0017601 Glaucomas HSDN C4085548 Usual severity dizziness C1134719 Invasive ductal breast carcinoma HSDN C0027498 Nausea vomiting C0030299 Pancreatic pseudocyst UMLS C0349588 Stature short C2931291 Familial spastic paraparesis and deafness OrphaNet|MalaCards C2911645 Weight loss adverse event C0024667 Animal mammary neoplasms HSDN C0042798 Vision dim C0010267 Cranial nerve neoplasms HSDN C4085548 Usual severity dizziness C0460137 Push down or depress HSDN C0522224 Palsied C0032966 Complication, neoplastic pregnancy HSDN C4085222 Nausea C0038395 Streptococcal infections HSDN C0018681 Headache, cephalalgia C1514197 Polycythemia vera, polycythemic phase UMLS C0030486 Extremity paralysis, lower C0006309 Brucellosis HSDN C0030193 Sense of pain C0521585 Gastrointestinal mucositis HSDN C4085211 Pain distress question C0677866 Brain stem neoplasms HSDN C0497406 Over weight C0011884 Diabetic retinopathy HSDN C4084784 Diarrhea C0206171 Community acquired infections HSDN C0011991 Loose stools C0014175 Endometriosis HSDN C0221170 Stiffness muscle C2936781 Generalized myotonia of thomsen HPO|UMLS C0020458 Hyperhydrosis C0029434 Osteogenesis imperfecta OrphaNet C4084802 Usual severity diarrhea C1963068 Atrial flutter adverse event HSDN C0424755 Fever symptoms C0015695 Fatty liver HSDN C0349588 Stature short C3711387 Autosomal recessive primary microcephaly OrphaNet|HPO|MalaCards C0026884 Muteness C0036349 Paranoid schizophrenia HSDN C1384666 Decreased hearing C1868678 Thanatophoric dysplasia, type i (disorder) OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0025294 Meningococcal meningitis HSDN C0013404 Respiratory difficulty C0238461 Anaplastic thyroid carcinoma UMLS C3665492 Pigmentations C1868679 Griscelli syndrome, type 2 MalaCards C0030552 Paralysis partial C0023418 Leukemia HSDN C0858572 Rigidity of limbs C1968556 Encephalopathy, neonatal severe, due to mecp2 mutations UMLS C1963170 Hypothermia adverse event C0016510 Foot diseases HSDN C0042798 Vision dim C0027877 Neuronal ceroid-lipofuscinoses OrphaNet|MalaCards C3244654 Sore throat brand of benzocaine & menthol C1527258 Infantile paralysis MalaCards C3539892 Pelvic pain in front C1881674 Medical device emits smoke HSDN C1963087 Constipation adverse event C1546635 Specimen source codes - fistula HSDN C0024031 Back pain lower back C0029455 Osteopoikilosis (disorder) HSDN C4084775 Usual severity weight loss C0162703 Pain sensitivity HSDN C3539890 Pelvic pain causes awakening at night C0020550 Hyperthyroidism HSDN C4084766 Vomiting C1963274 Vasculitis adverse event HSDN C4085211 Pain distress question C0036039 Sadism HSDN C0037763 Spasm C0268579 Propionic acidemia HSDN C3496180 Sleep apnea C1867858 Prader-willi syndrome chromosome region HPO C3815497 Cough C0018802 Congestive heart failure HSDN C0013604 Edematous C0005716 Blastomycosis HSDN C0314719 Dry eyes C3276706 Small fiber neuropathy MalaCards C1963087 Constipation adverse event C0497327 Dementia HSDN C0000737 Abdomen pain C0011849 Diabetes mellitus HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3714514 Infection HSDN C0520909 Ponv C0022660 Kidney failure, acute HSDN C1962956 Flatulence adverse event C0019284 Diaphragmatic hernia HSDN C2911645 Weight loss adverse event C0010692 Cystitis HSDN C0030193 Sense of pain C0033586 Failure, prosthesis HSDN C0022568 Inflammation corneal C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0001825 Agraphia C0936244 Developmental gerstmann syndrome MalaCards C0497406 Over weight C0033975 Psychotic disorders HSDN C3274924 Have been coughing C0997768 Glaucoma HSDN C0917816 Deficiency mental C0751435 Hyperphenylalaninaemia MalaCards C0476273 Distress respiratory C0340861 Electromechanical dissociation UMLS C1963091 Diarrhea adverse event C1959620 Dihydropyrimidine dehydrogenase deficiency HSDN C0012569 Double vision C0520946 Emotional hypersensitivity HSDN C2984058 Have pain C0040021 Thromboangiitis obliterans MalaCards C0018772 Deafness C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant HPO C1963091 Diarrhea adverse event C0022680 Polycystic kidney diseases HSDN C0004134 Dyssynergia C0026650 Movement disorders UMLS C0332563 Papulae C0023795 Lipoid proteinosis of urbach and wiethe OrphaNet|HPO C1963091 Diarrhea adverse event C1961100 Erectile dysfunction adverse event HSDN C0020578 Hyperventilate C0011334 Dental caries HSDN C0030200 Intractable pain C4049644 Depression HSDN C4084769 Vomiting frequency C0036982 Shock, hemorrhagic HSDN C3887873 Hearing loss C0001828 Agricultural workers' diseases HSDN C0027497 Queasy C0042384 Vasculitis HSDN C4084766 Vomiting C0042134 Uterine hemorrhage HSDN C3665347 Vision impaired C1847416 Friedreich ataxia with retained reflexes HPO C0018681 Headache, cephalalgia C0162820 Dermatitis, allergic contact HSDN C0018772 Deafness C3813607 Infantile gastroesophageal reflux HSDN C0349588 Stature short C2675859 Diamond-blackfan anemia 5 MalaCards C0012833 Dizzy C0151699 Intracranial hemorrhages HSDN C0349588 Stature short C2931653 Petty laxova wiedemann syndrome OrphaNet C4085317 Diarrhea frequency C1263846 Attention deficit hyperactivity disorder HSDN C4042891 Sleep wake disorders C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0036572 Convulsion C0342791 Carnitine-acylcarnitine translocase deficiency MalaCards|HPO|UMLS C0024031 Back pain lower back C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0027066 Myoclonic jerking C1843852 Spinocerebellar ataxia with epilepsy HPO C4085642 Level of joint stiffness C1846058 Lubs x-linked mental retardation syndrome HPO C0155347 Anomalies of divergence C2063486 Disorders of gaze UMLS C0030486 Extremity paralysis, lower C0005491 Biofeedback HSDN C0242936 Center pain C0242647 Mucosa-associated lymphoid tissue lymphoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0024215 Lymphangiectasis, intestinal HSDN C4085862 Bothered by nausea C2911643 Encounter due to family history of osteoporosis HSDN C0497406 Over weight C2937421 Prostatic hyperplasia HSDN C0030193 Sense of pain C0221757 Alpha 1-antitrypsin deficiency HSDN C0013604 Edematous C0149514 Bronchitis acute HSDN C0035078 Failure kidney C0079504 Hermanski-pudlak syndrome OrphaNet|HPO|MalaCards C0042798 Vision dim C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0086437 Joint hypermobility C4012146 Desbuquois dysplasia 1 MalaCards|UMLS C4084784 Diarrhea C0014547 Epilepsies, partial HSDN C0019572 Hairiness C0005941 Bone diseases, developmental HSDN C0009792 Consciousness disorder C0043253 Trauma blunt HSDN C0029645 Other insomnia C4237332 Other specified insomnia disorder UMLS C2030274 Heavy bleeding between periods C0524541 Deciduoma MalaCards C0031911 Pigment deposition C1857821 Leber congenital amaurosis 10 (disorder) MalaCards C1557397 Adverse event associated with pain C0206743 Rhabdoid tumor HSDN C0151786 Weakness muscle C0023518 Leukocytosis HSDN C2911647 Weight gain adverse event C2937287 Hematolysis HSDN C4084775 Usual severity weight loss C0032914 Pre-eclampsia HSDN C1557397 Adverse event associated with pain C1963068 Atrial flutter adverse event HSDN C0424755 Fever symptoms C0007133 Carcinoma, papillary HSDN C0013404 Respiratory difficulty C0268242 Niemann-pick disease, type a MalaCards C3163620 Hypotension adverse event C0206624 Hepatoblastoma MalaCards C0013404 Respiratory difficulty C0155866 Inhalational anthrax OrphaNet|MalaCards C4085317 Diarrhea frequency C0271972 Thiamine-responsive megaloblastic anemia MalaCards C4085317 Diarrhea frequency C0024525 Malacoplakia MalaCards C0746674 Muscle weakness generalized C0026764 Multiple myeloma OrphaNet|HPO C1963087 Constipation adverse event C0023890 Liver cirrhosis HSDN C0521629 Leucoplakia of male genital organs C0022782 Kraurosis penis UMLS C2911647 Weight gain adverse event C2937421 Prostatic hyperplasia HSDN C0497247 Blood pressure elevation C2931189 Neural crest tumor MalaCards C0013608 Cardiac edema C1176475 Ductal carcinoma HSDN C0029163 Hemorrhage mouth C0043397 Yellow fever, jungle MalaCards C0017565 Gingiva hemorrhage C0079504 Hermanski-pudlak syndrome HPO C0009806 Constipate C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0031142 Peritoneal diseases HSDN C4084776 Weight loss C0267963 Exocrine pancreatic insufficiency HSDN C0018681 Headache, cephalalgia C0025007 Measles HSDN C4084769 Vomiting frequency C3665596 Warts HSDN C0013404 Respiratory difficulty C0006267 Bronchiectasis UMLS C0040822 D tremors C4050613 Anxiety scale (basc-2) HSDN C0424755 Fever symptoms C0549567 Pigmentation disorders HSDN C2024893 Cardiovascular surgery result: fatigue C0016658 Fracture bone HSDN C0028738 Nystagmus C0271889 Diencephalic syndrome of infancy OrphaNet|MalaCards C0151825 Ostalgia C0014461 Granuloma eosinophilic MalaCards C0043094 Weight gain C0020615 Hypoglycemia HSDN C0031911 Pigment deposition C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0020672 Body temperature decreased C0013182 Drug allergy HSDN C0036659 Sensation disorder C0206762 Limb deformities, congenital HSDN C0022346 Yellow skin C0036341 Schizophrenia HSDN C1557397 Adverse event associated with pain C0036095 Salivary gland neoplasms HSDN C0042963 Symptoms vomiting C0033586 Failure, prosthesis HSDN C3887638 Failure to thrive in infant C0024814 Marinesco-sjogren syndrome MalaCards|HPO C0086565 Liver function abnormal C1291329 Transaldolase deficiency MalaCards|HPO C0003467 Angst C1849157 Insulin-like growth factor i, resistance to MalaCards|HPO C0162834 Hyperpigmentation C0162566 Porphyria cutanea tarda OrphaNet|MalaCards C4084766 Vomiting C0018794 Heart block HSDN C0151827 Pain eye C0220633 Uveal melanoma HPO C0004604 Pain back C1527336 Sjogren's syndrome HSDN C4084724 Usual severity constipation C0005967 Bone neoplasms HSDN C3539889 Pelvic pain increasing in severity C0012817 Diverticulum HSDN C0015230 Exanthem C1336015 Smoldering adult t-cell leukemia/lymphoma UMLS C4084773 Bothered by weight gain C0042029 Urinary tract infection HSDN C4084774 Have weight loss C0021799 Interprofessional relations HSDN C1963137 Hydrocephalus adverse event C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0030552 Paralysis partial C0751357 Focal myositides MalaCards C0020673 Hypothermia (central) (local) C0014556 Epilepsy, temporal lobe HSDN C0013404 Respiratory difficulty C0008628 Chromosome deletion HSDN C0344428 Ventricular tachycardia by ecg finding C3151204 Cardiomyopathy, familial hypertrophic, 16 HPO C0030552 Paralysis partial C0032344 Poisoning aspects HSDN C1069915 Vertigo C0025286 Meningioma HSDN C0424755 Fever symptoms C0008074 Child development disorders, pervasive HSDN C1999266 Depression adverse event C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0003862 Pain joint C0038015 Spondyloepiphyseal dysplasia MalaCards C0030232 Color loss C0024530 Malaria HSDN C4085211 Pain distress question C0027877 Neuronal ceroid-lipofuscinoses HSDN C1963184 Nystagmus adverse event C3809414 Cortical dysplasia, complex, with other brain malformations 3 MalaCards C0030193 Sense of pain C0585442 Osteosarcoma of bone HSDN C1279888 Proteinuria of undiagnosed cause C0020255 Hydrocephalus HSDN C2984058 Have pain C0035304 Retinal degeneration HSDN C2700617 Irritation - emotion C0016756 Fructose-1,6-diphosphatase deficiency MalaCards|HPO C2315100 Pediatric failure to thrive C1858302 Ectodermal dysplasia/ skin fragility syndrome OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0034088 Pulmonary valve insufficiency HSDN C0036659 Sensation disorder C0038941 Incisional infection HSDN C2315100 Pediatric failure to thrive C3279699 Encephalocardiomyopathy, mitochondrial, neonatal, due to atp synthase deficiency MalaCards C0151889 Reflexes tendon increased C2678046 Mental retardation, x-linked, syndromic, turner type HPO C0036572 Convulsion C0001623 Adrenal gland hypofunction HSDN C0036572 Convulsion C0005891 Bodies image HSDN C4084723 Constipation C0012979 Canine disease HSDN C2012605 Groin pain radiating to testicle C1861825 Cataract, posterior polar, 1 MalaCards C1963252 Tremor adverse event C0026139 Milk-sickness HSDN C0033377 Caudal displacement C2931390 Anophthalmia, cleft lip-palate, facial anomalies, and cns anomalies and hypothalamic disorder OrphaNet|MalaCards C0033774 Skin pruritus C0037397 Behavior social HSDN C0004941 Behavioral symptoms C0162309 Adrenoleukodystrophy OrphaNet C0917816 Deficiency mental C0342284 Bangstad syndrome OrphaNet|MalaCards C0008031 Pain chest C4085311 Depression - recess HSDN C1535893 Orthostatic intolerance C0002986 Fabry disease HSDN C0853986 Lymphocytes decreased C1744558 T-lymphocyte deficiency MalaCards C0349489 Fetal hypoxia C0001125 Acidosis, lactic HSDN C4084773 Bothered by weight gain C0206526 Tuberculosis, multidrug-resistant HSDN C0011570 Monopolar depression C1527406 Rhizomelic pseudopolyarthritis MalaCards C1963170 Hypothermia adverse event C0026640 Mouth neoplasms HSDN C1963137 Hydrocephalus adverse event C0796092 Oculo-cerebro-cutaneous syndrome OrphaNet|MalaCards C0011991 Loose stools C0022729 Klebsiella infections HSDN C4084768 Usual severity vomiting C0040247 Tinea HSDN C2911645 Weight loss adverse event C0039231 Tachycardia HSDN C1963087 Constipation adverse event C2931518 Plexosarcoma MalaCards C1279888 Proteinuria of undiagnosed cause C0017920 Glycogen storage disease type i MalaCards|HSDN|HPO C1279888 Proteinuria of undiagnosed cause C0242339 Dyslipidemias HSDN C1963091 Diarrhea adverse event C3146297 Study of behavior during childhood HSDN C3274924 Have been coughing C0001584 Adolescent psychology HSDN C0149741 Nipple discharge C0405479 Disorders nipple UMLS C0004134 Dyssynergia C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) OrphaNet|HPO|MalaCards C0007859 Pain neck C1090821 Sepsis (invertebrate) HSDN C0040264 Ear ringing sound C0206719 Central neurocytoma MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0003509 Aortitis, nos HSDN C0018784 Deafness sensorineural C1306710 Facial asymmetry HSDN C0036572 Convulsion C1546949 Event consequence - death HSDN C4084776 Weight loss C1302282 Chromaffin cell neoplasm MalaCards C0000727 Abdomen acute C0023798 Lipoma HSDN C1145670 Failure respiratory C0751918 Cockayne pelizaeus merzbacher disease MalaCards C2984058 Have pain C0041330 Tuberculosis, spinal HSDN C4084897 Sleep disturbance subordinate domain C0751664 Canavan disease, neonatal OrphaNet|HPO C0557874 Global developmental delay C1851443 Cerebrooculofacioskeletal syndrome 3 MalaCards C1963093 Dizziness adverse event C0035439 Rheumatic heart disease HSDN C0010200 Cough symptom C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1963154 Renal failure adverse event C0376359 Groenblad-strandberg syndrome MalaCards C0018775 Hearing loss bilateral C0036341 Schizophrenia HSDN C0152459 Striae C0006267 Bronchiectasis HSDN C2984058 Have pain C0041976 Urethritis HSDN C0023012 Delay language C0342727 3-@methylglutaconic aciduria, type i OrphaNet|HPO|MalaCards C0042571 Vertigo subjective C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4084784 Diarrhea C0276932 Schistosoma; intercalatum DiseaseOntology C1963281 Vomiting adverse event C0008065 Childhood behavior HSDN C4084766 Vomiting C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0231341 Aging premature C3850148 Vascular remodeling HSDN C4084767 Bothered by vomiting C0007873 Uterine cervical neoplasm HSDN C4084723 Constipation C0005586 Bipolar disorder HSDN C4085210 Usual severity pain C0018916 Hemangioma HSDN C0020538 Hbp C1706004 Anhydrotic ectodermal dysplasias MalaCards C1963091 Diarrhea adverse event C0005396 Bile duct neoplasms HSDN C2203646 Jaundice C0019196 Hepatitis c DiseaseOntology|HSDN|MalaCards C4084775 Usual severity weight loss C0206081 Hyperandrogenism HSDN C0424755 Fever symptoms C0008149 Chlamydia infections HSDN C4084774 Have weight loss C0034494 Rabies (disorder) HSDN C0518090 Frequency of pain question C0020433 Hyperbilirubinemia HSDN C1263846 Attention deficit disorder with hyperactivity C2937288 Thyroid hormone resistance, generalized, autosomal dominant HPO C4085231 Usual severity difficulty swallowing C0396023 Chronic adenoiditis DiseaseOntology|MalaCards C0037384 Snore C0007097 Carcinomas HSDN C0917816 Deficiency mental C0549567 Pigmentation disorders MalaCards C2984057 Have nausea C0029184 Orbital fracture HSDN C4085317 Diarrhea frequency C0023530 Leukopenia HSDN C0423714 Genitofemoral nerve neuralgia C1290866 Disease of pelvis UMLS C0424755 Fever symptoms C3489393 Hiatal hernia HSDN C0042755 Virilisation C0405580 Adrenal cortical hypofunction HSDN C3539020 Pelvic pain decreasing in frequency C0006118 Brain neoplasms HSDN C0026838 Spasticity muscle C1839130 Dystonia 3, torsion, x-linked HSDN C0007166 Cardiac output decreased C0013069 Double outlet right ventricle HSDN C0020305 Fetal edema C0432201 Boomerang dysplasia OrphaNet|HPO|MalaCards C2984058 Have pain C0027531 Neck injury HSDN C1279888 Proteinuria of undiagnosed cause C0740394 Hyperuricemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0237104 Spirituality HSDN C4084766 Vomiting C1857728 Hereditary angioedema type iii MalaCards|HPO C0013604 Edematous C0023904 Liver neoplasms, experimental HSDN C4084776 Weight loss C0243013 Base learn problems HSDN C1971624 Appetite absent C3541306 Plasmodium measurement HSDN C0020615 Hypoglycemia nos C0796154 Simpson-golabi-behmel syndrome, type 1 OrphaNet|HPO|MalaCards C0023530 Leukopenia C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C0030975 Disorders perception C3810814 Myocardial infarction ecg assessment HSDN C0009763 Conjunctiva inflammation C0343206 Hypocomplementemic urticarial vasculitis MalaCards C4084724 Usual severity constipation C0010695 Cystocele HSDN C1963071 Back pain adverse event C0036974 Shock HSDN C0011570 Monopolar depression C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C0030193 Sense of pain C0009730 Spinal meningocele HSDN C0576456 Poor feeding C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards C2919142 Short stature adverse event C1848912 Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage MalaCards C0016382 Cutaneous vascular engorgement C1852542 Cdo syndrome MalaCards C0151686 Growth retardation C3887877 Deficiency of glycerate kinase MalaCards C1963184 Nystagmus adverse event C3554690 Ataxia-oculomotor apraxia 3 MalaCards C0013421 Dystonia C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C0002170 Alopecia disorders C1843292 Skin fragility-woolly hair syndrome MalaCards|HPO C0236065 Edema mouth C0410013 Soft tissue lesion UMLS C0518090 Frequency of pain question C1419157 Pygm gene HSDN C3665492 Pigmentations C0027809 Neurilemmoma MalaCards C0039070 Collapse fleeting C0007137 Squamous cell carcinoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029944 Drug overdose HSDN C1963087 Constipation adverse event C0007193 Cardiomyopathy, dilated HSDN C4084775 Usual severity weight loss C0027583 Nematode infections HSDN C0026821 Cramp C0553604 Myotonic disorders HSDN C3665347 Vision impaired C1623209 Okihiro syndrome MalaCards C0035229 Respiratory function impaired C0282577 Congenital disorders of glycosylation MalaCards C3641756 Have diarrhea C0030807 Pemphigus, nos HSDN C0005779 Clotting C1835849 Congenital disorder of glycosylation, type im OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0006114 Cerebral edema HSDN C2911645 Weight loss adverse event C0034040 Puerperal disorders HSDN C0151786 Weakness muscle C0268450 Gitelman syndrome HSDN C4084773 Bothered by weight gain C0031090 Periodontal diseases HSDN C0013604 Edematous C1720777 Functional laterality HSDN C4084802 Usual severity diarrhea C0031347 Pharyngeal neoplasms HSDN C3541349 Syncope C1258104 Diffuse scleroderma HSDN C0035232 Diaphragmatic paralysis C0006057 Botulisms OrphaNet|MalaCards C0033074 Presbycusis C0011854 Diabetes mellitus, insulin-dependent HSDN C4084766 Vomiting C0086543 Cataract nos HSDN C4084802 Usual severity diarrhea C0018565 Acquired deformity of hand, nos HSDN C4085210 Usual severity pain C0020555 Hypertrichosis HSDN C4084784 Diarrhea C0034013 Precocious puberty HSDN C0034933 Abnormal reflexes C0051981 Anti-leprosy vaccine HSDN C0518090 Frequency of pain question C0023976 Long qt syndrome HSDN C0003079 Pupillary inequality C0025295 Meningitis, pneumococcal HSDN C0948426 Bowel peristalsis increased C0948395 Gastrointestinal hypermotility UMLS C1963154 Renal failure adverse event C0033847 Pseudoxanthoma elasticum MalaCards C1279888 Proteinuria of undiagnosed cause C0268251 Gaucher disease, type 3 (disorder) MalaCards|HPO C1963252 Tremor adverse event C0035242 Respiratory tract diseases HSDN C0036572 Convulsion C3463897 Hydatidiform mole, recurrent, 1 HSDN C0042798 Vision dim C2931803 Deletion 11p13 OrphaNet|HPO C0036572 Convulsion C0221033 Trisomy x syndrome MalaCards C0042928 Paralysis vocal cord C0376527 Neoplasm, skull base HSDN C0086437 Joint hypermobility C0016667 Fragile x syndrome OrphaNet|UMLS|HPO|MalaCards C0242936 Center pain C0039336 Gustatory sense HSDN C3898969 Have been vomiting C1963067 Atrial fibrillation adverse event HSDN C0030193 Sense of pain C0264675 Angina pectoris class i UMLS C4084725 Usual severity cough C0015397 Disorder of eye HSDN C1963065 Apnea adverse event C0032962 Pregnancy complications HSDN C0242936 Center pain C0033806 Pseudohypoparathyroidism HSDN C2096293 Ent surgical result ear vertigo C0033817 Pseudomonas infections HSDN C0011206 Delirium acute C0000833 Abscess HSDN C4084768 Usual severity vomiting C0020676 Hypothyroidism HSDN C3463815 Feel fatigue C0026598 Movement perception HSDN C2984058 Have pain C0014849 Esophageal and gastric varices HSDN C0036572 Convulsion C3280452 Spinocerebellar ataxia, autosomal recessive 12 MalaCards|UMLS C4084773 Bothered by weight gain C0016053 Fibromyalgia HSDN C0206146 Myocardial stunning C0340293 Anterior myocardial infarction HSDN C0151825 Ostalgia C1960539 Aromatase deficiency OrphaNet|HPO|MalaCards C0011991 Loose stools C0003855 Arteriovenous fistula HSDN C0030975 Disorders perception C0014556 Epilepsy, temporal lobe HSDN C2911645 Weight loss adverse event C0030567 Parkinson disease HSDN C0042571 Vertigo subjective C1565489 Renal insufficiency HSDN C0016204 Fart C0037650 Somatoform disorder HSDN C0013390 Cramps menstrual C0027643 Neoplasm recurrence, local HSDN C0020458 Hyperhydrosis C2931689 Dystrophia myotonica 2 MalaCards C0019079 Bloody sputum C1332165 Adenocarcinoma and small cell carcinoma of lung UMLS C0042384 Vasculitis, nonspecific C0040021 Thromboangiitis obliterans OrphaNet|MalaCards C0423818 Grooving of nail C0406557 Poikiloderma of kindler MalaCards|UMLS C2315100 Pediatric failure to thrive C0175694 Smith-lemli-opitz syndrome MalaCards|HSDN|HPO C0018681 Headache, cephalalgia C0007570 Celiac disease HSDN C1000483 Genus anemia C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0007798 Cerebral ventricle neoplasm HSDN C0036572 Convulsion C1963059 Adrenal insufficiency adverse event HSDN C2315100 Pediatric failure to thrive C1439329 Cbs gene HPO C0015469 Facial paralysis C1837091 Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0155490 Middle ear cholesteatoma HSDN C0522224 Palsied C0030612 Milk fever HSDN C0018834 Brash C0751157 Fraxe syndrome MalaCards C0085593 Chill C0085399 Ehrlichiosis HSDN C0020903 Illusion C0024195 Deceptiveness HSDN C4084724 Usual severity constipation C3266898 Waardenburg syndrome OrphaNet|HPO C4084726 Distress cough C0033860 Psoriasis HSDN C0042798 Vision dim C0265241 Franceschetti-klein syndrome OrphaNet|HPO|MalaCards C0024031 Back pain lower back C0002453 Amenorrhea HSDN C0038990 Sweats C0036161 Sandhoff disease HPO C0349588 Stature short C0795959 Gomez lopez hernandez syndrome OrphaNet|MalaCards C0030552 Paralysis partial C0042075 Urologic diseases HSDN C0007758 Cerebellar ataxia C2985524 Rhabdoid tumor predisposition syndrome MalaCards C0036572 Convulsion C0015934 Fetal growth retardation MalaCards|HSDN C0016199 Pain flank C0003496 Aortic rupture HSDN C0018772 Deafness C0001486 Adenovirus infections HSDN C2984058 Have pain C0019151 Hepatic encephalopathy HSDN C3898969 Have been vomiting C0003873 Rheumatoid arthritis HSDN C0030554 Abnormal sensation C0023176 Lead poisoning MalaCards C4084774 Have weight loss C1457883 Aggressive reaction HSDN C0037316 Not enough sleeping C0007785 Cerebral infarction HSDN C4084773 Bothered by weight gain C0600041 Infective cystitis HSDN C0270948 Neurogenic muscular atrophy C0751072 Frontotemporal lobar degeneration MalaCards C0018681 Headache, cephalalgia C1809471 Familial benign hypercalcemia MalaCards C4084766 Vomiting C0085207 Gestational diabetes HSDN C2024878 Cardiovascular surgery result: dyspnea C0018193 Granuloma, foreign-body HSDN C2919142 Short stature adverse event C0392475 Roberts-sc phocomelia syndrome HPO C0020649 Blood pressure decreased C0854795 Resectable hepatic malignant neoplasm MalaCards C0151311 Cranial nerve palsy C0392475 Roberts-sc phocomelia syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0042214 Vaccinia HSDN C0030193 Sense of pain C0085693 Acute appendicitis nos (disorder) MalaCards C0015970 Fever unknown origin C0276275 Disease due to parvoviridae HSDN C2911645 Weight loss adverse event C0001815 Primary myelofibrosis HSDN C2024878 Cardiovascular surgery result: dyspnea C1623041 Breast-fed HSDN C0036659 Sensation disorder C0596306 Chemical association HSDN C3541349 Syncope C3539760 Mok wt allele HSDN C0018681 Headache, cephalalgia C0016510 Foot diseases HSDN C0424755 Fever symptoms C0037998 Splenic infarction HSDN C4084774 Have weight loss C0520946 Emotional hypersensitivity HSDN C0042025 Urinary incontinence stress C0038395 Streptococcal infections HSDN C4084787 Have difficulty swallowing C0032372 Poliomyelitis, anterior, acute DiseaseOntology|MalaCards C1963170 Hypothermia adverse event C0039336 Gustatory sense HSDN C0007758 Cerebellar ataxia C1848578 Methylmalonic aciduria and homocystinuria, cblf type (disorder) OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0020507 Hyperplasia HSDN C0008031 Pain chest C2984299 Asthma pathway HSDN C1963252 Tremor adverse event C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0010200 Cough symptom C0243025 Hantavirus pulmonary syndrome MalaCards C0024031 Back pain lower back C0002395 Alzheimer's disease HSDN C4084774 Have weight loss C0014038 Encephalitis HSDN C3539022 Pelvic pain decreasing in severity C1547940 Specimen source codes - ulcer HSDN C3641756 Have diarrhea C0018482 Haemophilus infections HSDN C0009676 Confusion state C1290398 Cerebral arterial aneurysm HSDN C0004604 Pain back C0024586 Malignant carcinoid syndrome HSDN C0018524 Hallucinate C0085632 Apathy HSDN C0036572 Convulsion C0270833 Simple partial seizure with disturbance of higher cerebral function UMLS C2984058 Have pain C0008309 Bile duct adenoma HSDN C4084723 Constipation C0042769 Virus diseases HSDN C3541349 Syncope C0001175 Acquired immunodeficiency syndrome HSDN C1557397 Adverse event associated with pain C0020540 Malignant hypertension HSDN C4084724 Usual severity constipation C1846058 Lubs x-linked mental retardation syndrome HPO C3665347 Vision impaired C2931673 Ceroid lipofuscinosis, neuronal 1, infantile OrphaNet|MalaCards C0017672 Pain tongue C0344315 Depressed mood HSDN C0036572 Convulsion C0393693 Benign neonatal epilepsy, nonfamilial UMLS C0018772 Deafness C0271650 Impaired glucose tolerance HSDN C2024893 Cardiovascular surgery result: fatigue C0033375 Prolactinoma OrphaNet|HPO|MalaCards C0243026 Generalized infection C0016952 Galactosemias OrphaNet|MalaCards C0042384 Vasculitis, nonspecific C2347126 Microscopic polyarteritis MalaCards C4084769 Vomiting frequency C0085278 Antiphospholipid syndrome HSDN C0518090 Frequency of pain question C2028283 History of premature birth HSDN C1963091 Diarrhea adverse event C2937421 Prostatic hyperplasia HSDN C4084776 Weight loss C0878544 Cardiomyopathies HSDN C3541349 Syncope C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) MalaCards|HPO C0151798 Liver necrosis C0023903 Liver neoplasms MalaCards C0028738 Nystagmus C1832162 Hypotrichosis, congenital, with juvenile macular dystrophy MalaCards|HPO C0036659 Sensation disorder C1963178 Myelitis adverse event HSDN C2911645 Weight loss adverse event C0021568 Bites insect stings HSDN C0242670 Chronic vegetative state C0085094 Head injury closed HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C2973725 Pulmonary arterial hypertension OrphaNet C0162298 Stiffness joints C1968748 Gangliosidosis, generalized gm1, type i, with cardiac involvement HPO C4084768 Usual severity vomiting C0596170 Binge eating disorder HSDN C4020887 Photodysphoria C2931753 Achromatopsia incomplete, x-linked MalaCards|HPO C0004134 Dyssynergia C0014457 Eosinophilia HSDN C3809715 Epistaxis recurrent C1857688 Telangiectasia, hereditary hemorrhagic, type 4 MalaCards C0015230 Exanthem C2711496 Cutaneous larva migrans due to uncinaria UMLS C1963093 Dizziness adverse event C0035334 Retinitis pigmentosa HSDN C0036572 Convulsion C0032708 Disorders of porphyrin metabolism MalaCards|HSDN C1279888 Proteinuria of undiagnosed cause C0242528 Azotemia HSDN C3274924 Have been coughing C0037274 Dermatologic disorders HSDN C2096293 Ent surgical result ear vertigo C0042373 Vascular diseases HSDN C1963093 Dizziness adverse event C0027947 Neutropenia HSDN C3539020 Pelvic pain decreasing in frequency C0014179 Endometritis HSDN C0557874 Global developmental delay C2678480 Chromosome 22q11.2 deletion syndrome, distal OrphaNet|HPO|MalaCards C0162298 Stiffness joints C1855305 Ter haar syndrome MalaCards C0018681 Headache, cephalalgia C0036864 Sexual relations HSDN C3665386 Abnormal vision C1843920 Coenzyme q10 deficiency HPO C0333422 Gumma C0546351 Sporotrichotic gumma UMLS C0032617 High urine output C2748440 Sensorineural deafness with mild renal dysfunction HPO C0017181 Gastrointestinal bleed C0032463 Polycythemia vera HPO C0030975 Disorders perception C0031996 Discrimination, pitch HSDN C1963184 Nystagmus adverse event C0812437 Oculo-dento-digital syndrome MalaCards|HPO C2936821 Spinal cerebrospinal fluid leak C0020258 Hydrocephalus, normal pressure HSDN C0751837 Gait ataxic C0205833 Medullomyoblastoma UMLS C1963281 Vomiting adverse event C0525045 Mood disorders HSDN C0237326 Defecation pain C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0013404 Respiratory difficulty C0019209 Hepatomegaly HSDN C0413252 Hypothermia due to exposure C3810814 Myocardial infarction ecg assessment HSDN C4084742 Bothered by night sweats C0024586 Malignant carcinoid syndrome MalaCards C0034150 Skin purpura C1948007 Pityriasis HSDN C0041657 Consciousness loss C0009450 Disease caused by microorganism HSDN C4085211 Pain distress question C0152427 Polydactyly HSDN C1963249 Tinnitus adverse event C2981150 Uranostaphyloschisis HSDN C3815497 Cough C0033348 Language program HSDN C0042384 Vasculitis, nonspecific C0403529 Anti-glomerular basement membrane disease OrphaNet|MalaCards C0002622 Amnesias C0033941 Psychoses, substance-induced HSDN C0027796 Neuralgias C1720149 Neuralgia associated with aids UMLS C0242936 Center pain C0013712 Ego HSDN C1963063 Anorexia adverse event C0043398 Yellow fever, urban MalaCards C0000727 Abdomen acute C0267400 Acute haemorrhagic enterocolitis UMLS C0030486 Extremity paralysis, lower C1548483 Leishmaniasis vaccine HSDN C1963170 Hypothermia adverse event C0340629 Aortic aneurysm without mention of rupture nos HSDN C0042798 Vision dim C1275685 Avellino corneal dystrophy MalaCards|HPO C0008031 Pain chest C0020542 Pulmonary hypertension HSDN C0024031 Back pain lower back C1861172 Venous thromboembolism HSDN C2237041 Shox gene with short stature C1415737 Hsd11b2 gene HPO C1963184 Nystagmus adverse event C1832588 Chromosome 11p11.2 deletion syndrome OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0007131 Non-small cell lung carcinoma HSDN C0427068 Legs weakness C1838192 Spastic paraplegia 6, autosomal dominant (disorder) MalaCards|HPO C0917816 Deficiency mental C0432283 Osteoglophonic dwarfism MalaCards|HPO C0027796 Neuralgias C0022660 Kidney failure, acute HSDN C0020615 Hypoglycemia nos C1414525 Fah gene HPO C3641756 Have diarrhea C0016053 Fibromyalgia HSDN C4085211 Pain distress question C0037116 Silicosis HSDN C0042963 Symptoms vomiting C0175683 Citrullinemia HPO|UMLS C1963091 Diarrhea adverse event C0042384 Vasculitis HSDN C0018681 Headache, cephalalgia C0009946 Conversion disorder HSDN C2911647 Weight gain adverse event C0018798 Congenital heart defects HSDN C0010038 Corneal opacity disorder C0393590 Fahr's syndrome (disorder) OrphaNet|HPO|MalaCards C4085211 Pain distress question C2028283 History of premature birth HSDN C4084767 Bothered by vomiting C0023676 Life style HSDN C0043094 Weight gain C0033923 Psychomotor function HSDN C2203646 Jaundice C0037356 Smallpox virus HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C2677491 Cardiomyopathy, familial hypertrophic, 12 HPO C0036396 Sciatica C0029401 Osteitis deformans HSDN C0150055 Pain chronic C0013394 Coitus painful HSDN C0242936 Center pain C0010072 Coronary thrombosis HSDN C0027497 Queasy C0010709 Cyst HSDN C4084769 Vomiting frequency C0010481 Cushing syndrome HSDN C4084766 Vomiting C0013514 Echinostomiasis DiseaseOntology C0030552 Paralysis partial C0034040 Puerperal disorders HSDN C0030193 Sense of pain C1963282 Wolff-parkinson-white syndrome adverse event HSDN C1260880 Nasal drip C1336389 Stage ivb accessory sinus carcinoma UMLS C4085211 Pain distress question C0029463 Osteosarcoma OrphaNet|HSDN|HPO C0035229 Respiratory function impaired C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0033774 Skin pruritus C0030491 Parapsoriasis HSDN C4085211 Pain distress question C0520459 Necrotizing enterocolitis HSDN C4084769 Vomiting frequency C0025290 Aseptic meningitis HSDN C0012833 Dizzy C0149721 Left ventricular hypertrophy HSDN C1557397 Adverse event associated with pain C0015395 Burn eye HSDN C0009421 Comatose C1306571 Hepatic insufficiency HSDN C0004134 Dyssynergia C1851443 Cerebrooculofacioskeletal syndrome 3 HPO C0242936 Center pain C0001173 Adult pyloric stenosis HSDN C0424755 Fever symptoms C0029458 Osteoporosis, postmenopausal HSDN C0522224 Palsied C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C2203646 Jaundice C0151516 Thyroid hypoplasia OrphaNet|HPO C0020455 Hypergammaglobulinemia C1253943 Fluid in the chest HSDN C2984058 Have pain C0015461 Facial neoplasms HSDN C2237041 Shox gene with short stature C0342280 Aredyld OrphaNet|MalaCards C0522224 Palsied C0018081 Gonorrhea HSDN C1963087 Constipation adverse event C0001721 Emotional affect HSDN C3274924 Have been coughing C0023448 Lymphoid leukemia HSDN C1963087 Constipation adverse event C0262655 Recurrent urinary tract infection HSDN C0019214 Hepatosplenomegaly C1835912 Aicardi-goutieres syndrome 4 MalaCards|HPO C1963087 Constipation adverse event C0029456 Osteoporosis HSDN C0036572 Convulsion C3280127 Mental retardation, autosomal recessive 15 MalaCards C4085210 Usual severity pain C0025464 Mesenchymoma HSDN C0012833 Dizzy C0271829 Pendred's syndrome MalaCards|HPO C4084784 Diarrhea C1856143 Hemolytic uremic syndrome, typical MalaCards C0032227 Effusion pleural C0342623 Senile systemic amyloidosis MalaCards C0015970 Fever unknown origin C0034359 Cell pus urine HSDN C1384666 Decreased hearing C0338508 Optic atrophy, autosomal dominant HSDN C3887638 Failure to thrive in infant C0700095 Central neuroblastoma MalaCards C0518090 Frequency of pain question C0041972 Urethral obstruction HSDN C1557397 Adverse event associated with pain C0033348 Language program HSDN C0700590 Diaphoresis excessive C1832600 Naxos disease OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0039263 Takayasu arteritis HSDN C3887873 Hearing loss C4085311 Depression - recess HSDN C2203646 Jaundice C0043515 Zollinger-ellison syndrome MalaCards C0239819 Hand edema C0542571 Facial edema UMLS C4085548 Usual severity dizziness C0022665 Kidney neoplasm HSDN C1557397 Adverse event associated with pain C0026010 Microphthalmos HSDN C0003862 Pain joint C0029458 Osteoporosis, postmenopausal HSDN C0424755 Fever symptoms C0016171 Fistula of intestine, excluding rectum and anus HSDN C0003550 Broca aphasia C0009240 Cognition HSDN C4085317 Diarrhea frequency C0002063 Alkalosis HSDN C0018989 Paresis of one side of body C1762616 Meningioma, benign, no icd-o subtype MalaCards C0019825 Voice hoarseness C0220765 Weaver-like syndrome MalaCards C0234146 Absent reflex C3554398 Spinal muscular atrophy, jokela type MalaCards C0036572 Convulsion C2350521 Gustatory perception HSDN C3815497 Cough C0034362 Q fever DiseaseOntology|MalaCards C0851578 Disorder sleep C0024636 Malocclusion HSDN C4084726 Distress cough C0270611 Brain damage HSDN C0043094 Weight gain C0031099 Periodontitis HSDN C4085222 Nausea C0015457 Expression facial HSDN C0018784 Deafness sensorineural C3541306 Plasmodium measurement HSDN C0010200 Cough symptom C0011860 Diabetes mellitus, non-insulin-dependent HSDN|UMLS C3665386 Abnormal vision C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome OrphaNet|HPO|MalaCards C0004604 Pain back C0007117 Basal cell carcinoma HSDN C2984058 Have pain C1691228 Cystic kidney diseases HSDN C0497247 Blood pressure elevation C4015130 Inflammatory skin and bowel disease, neonatal, 2 MalaCards C0085593 Chill C0085293 Hepatitis e HSDN C0206160 Retic count elevated C0242188 Spider bites HSDN C0576456 Poor feeding C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C0151827 Pain eye C0997768 Glaucoma HSDN C0002170 Alopecia disorders C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0035222 Respiratory distress syndrome, adult HSDN C2984058 Have pain C0344435 Ventricular fibrillation by ecg finding HSDN C0020673 Hypothermia (central) (local) C0009450 Disease caused by microorganism HSDN C0557874 Global developmental delay C0268242 Niemann-pick disease, type a MalaCards|HPO C0015468 Face pain C0027858 Neuroma HSDN C4085210 Usual severity pain C0018021 Goiter HSDN C0557874 Global developmental delay C2931454 Conductive hearing loss and malformed low-set ears OrphaNet|MalaCards C4084725 Usual severity cough C0043254 Injuries penetrating HSDN C0008031 Pain chest C1998095 Epizootic lymphangitis MalaCards C0011175 Deficient fluid volume C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C0037771 Paraparesis spastic C0751604 Hereditary x-linked recessive spastic paraplegia MalaCards C4084724 Usual severity constipation C0007134 Renal cell carcinoma HSDN C0030486 Extremity paralysis, lower C0019196 Hepatitis c HSDN C2911647 Weight gain adverse event C0036330 Schistosomiasis mansoni HSDN C0497406 Over weight C0002895 Anemia, sickle cell HSDN C4084724 Usual severity constipation C0021361 Female infertility HSDN C0042928 Paralysis vocal cord C0026764 Multiple myeloma HSDN C0000737 Abdomen pain C0000832 Abruptio placentae HSDN C1557397 Adverse event associated with pain C0019342 Genital herpes HSDN C0010520 Skin cyanosis C0004352 Autistic disorder HSDN C0018681 Headache, cephalalgia C0008073 Developmental disabilities HSDN C0575081 Abnormal gait C2931227 Rivera perez salas syndrome MalaCards C0460137 Push down or depress C2930815 Acute cerebral gaucher disease MalaCards C0009421 Comatose C0751666 Canavan disease, infantile OrphaNet|HPO C0036572 Convulsion C1840334 Hypoparathyroidism, autosomal recessive MalaCards|HPO C0751295 Memory loss or impairment C2986550 Pituicytoma MalaCards C4084727 Cough frequency C0334511 Pleural solitary fibrous tumor HSDN C1962972 Proteinuria adverse event C0020503 Hyperparathyroidism, secondary HSDN C1557397 Adverse event associated with pain C0162836 Hidradenitis suppurativa HSDN C0018681 Headache, cephalalgia C2706915 Language:-:point in time:^patient:- HSDN C0033774 Skin pruritus C0577628 Latex allergy HSDN C3815497 Cough C1963198 Pancreatitis adverse event HSDN C0024031 Back pain lower back C1963084 Colitis adverse event HSDN C0042963 Symptoms vomiting C0268242 Niemann-pick disease, type a MalaCards|HPO|UMLS C0086439 Activity decreased C0006118 Brain neoplasms HSDN C4084767 Bothered by vomiting C0039841 Thiamine deficiency HSDN C4084788 Have dizziness C0034065 Pulmonary embolism HSDN C3641756 Have diarrhea C1456781 Benign melanocytic nevus HSDN C0011991 Loose stools C0020255 Hydrocephalus HSDN C0042963 Symptoms vomiting C0334489 Pancreatoblastoma OrphaNet|MalaCards C4085642 Level of joint stiffness C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C0344242 Monocular nystagmus C0028738 Nystagmus UMLS C0013395 Indigestion C2987396 Gastric hepatoid adenocarcinoma UMLS C0012833 Dizzy C0002438 Amebiasis HSDN C3541349 Syncope C0036946 Sheep--diseases HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0036439 Scoliosis, unspecified HSDN C0007758 Cerebellar ataxia C1846790 Joubert syndrome 4 (disorder) MalaCards|HPO C2919142 Short stature adverse event C3275495 Kabuk2 MalaCards C0026838 Spasticity muscle C4225247 Leukodystrophy, hypomyelinating, 12 UMLS C0026826 High muscle tone C2752008 Spastic paraplegia-50, autosomal recessive MalaCards C0277959 Hair coarseness C0086647 Mucopolysaccharidosis type iiia MalaCards|HPO C0036572 Convulsion C0037355 Smallpox vaccines HSDN C2029884 Hearing loss by exam C0006434 Burn injury HSDN C4085317 Diarrhea frequency C0348018 Projections HSDN C0023012 Delay language C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C0036572 Convulsion C0010051 Coronary aneurysm HSDN C1963087 Constipation adverse event C0242342 Sheehan syndrome MalaCards C4085211 Pain distress question C0030567 Parkinson disease HSDN C2029884 Hearing loss by exam C0007820 Cerebrovascular disorders HSDN C4042891 Sleep wake disorders C0030977 Perceptual masking HSDN C0040822 D tremors C1855109 Methylmalonic aciduria cbla type HPO|UMLS C0018681 Headache, cephalalgia C3661801 Chronic migraine without aura with status migrainosus UMLS C1963170 Hypothermia adverse event C0020461 Hyperkalemia HSDN C1279888 Proteinuria of undiagnosed cause C1550639 Specimen type - fistula HSDN C0848203 Male pelvic pain C1963088 Cystitis adverse event HSDN C0032285 Pneum C1279945 Acute interstitial pneumonia MalaCards C1963252 Tremor adverse event C0038868 Progressive supranuclear palsy HPO C0085649 Edema extremities C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome OrphaNet|HPO|MalaCards C0040485 Wryneck C0475073 Subarachnoid hemorrhage traumatic HSDN C0004134 Dyssynergia C0034341 Pyruvate carboxylase deficiency disease HSDN C0000727 Abdomen acute C0009062 Clostridia infection HSDN C2237041 Shox gene with short stature C0795841 Jacobsen distal 11q deletion syndrome OrphaNet|HPO|MalaCards C3665492 Pigmentations C1847800 Waardenburg syndrome type 1 MalaCards C4085549 Dizziness C0004936 Mental disorders HSDN C4084768 Usual severity vomiting C0016171 Fistula of intestine, excluding rectum and anus HSDN C4084769 Vomiting frequency C0018805 Heart injuries HSDN C3274924 Have been coughing C0031117 Peripheral neuropathy HSDN C0401149 Constipation chronic C2939462 Immunoglobulin deposition disease MalaCards C0392156 Acathesia C0876984 Akathisia aggravated UMLS C0028738 Nystagmus C3495551 Dihydropyrimidinuria MalaCards C0023012 Delay language C3539494 Spastic paraplegia 53, autosomal recessive MalaCards C0018772 Deafness C1304205 Neutrophilic urticaria MalaCards C0018524 Hallucinate C1847987 Huntington disease-like 2 MalaCards|HPO C3641756 Have diarrhea C0037355 Smallpox vaccines HSDN C0040034 Thrombocytopenia C1855126 3-methylglutaconic aciduria type iv MalaCards C4085210 Usual severity pain C0018418 Gynecomastia HSDN C0085593 Chill C0020473 Hyperlipidemia UMLS C2911645 Weight loss adverse event C2984302 Leishmaniasis infection pathway HSDN C1384666 Decreased hearing C0175691 Dubowitz syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0001957 Alcohol withdrawal delirium HSDN C0013395 Indigestion C0009450 Disease caused by microorganism HSDN C0003862 Pain joint C0002986 Fabry disease OrphaNet|HPO|MalaCards C0000727 Abdomen acute C1134719 Invasive ductal breast carcinoma HSDN C3887638 Failure to thrive in infant C0005956 Bone marrow diseases HSDN C0018991 Paralysis one side of body C0011581 Depressive disorder HSDN C1963071 Back pain adverse event C0006840 Candidiasis HSDN C0020673 Hypothermia (central) (local) C1299262 Sarcoma - category (morphologic abnormality) HSDN C0575081 Abnormal gait C1837713 Joubert syndrome 3 MalaCards C2237041 Shox gene with short stature C0796137 3c syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C2936350 Plaque, atherosclerotic HSDN C0030486 Extremity paralysis, lower C0015927 Intrauterine fetal demise HSDN C0027066 Myoclonic jerking C4049994 Insulin resistance measurement HSDN C0034150 Skin purpura C1306214 Acth-secreting pituitary adenoma HPO C0019572 Hairiness C0270611 Brain damage HSDN C3815497 Cough C0038587 Substance withdrawal syndrome HSDN C2364111 Gustatory anesthesia C0040261 Onychomycosis HSDN C0009398 Color vision defects C3665342 Progressive cone dystrophy MalaCards C0002170 Alopecia disorders C1854698 Multiple carboxylase deficiency, juvenile-onset OrphaNet|HPO|MalaCards C0020649 Blood pressure decreased C0239981 Hypoalbuminemia MalaCards C2984058 Have pain C0033595 Prostitution HSDN C0020673 Hypothermia (central) (local) C1963090 Dehydration adverse event HSDN C3898969 Have been vomiting C0002880 Autoimmune hemolytic anemia HSDN C0035229 Respiratory function impaired C0005283 Beta thalassemia OrphaNet C4085210 Usual severity pain C0038002 Splenomegaly HSDN C4085317 Diarrhea frequency C0033700 Infection proteus HSDN C1971624 Appetite absent C0025202 Melanoma HSDN C0010520 Skin cyanosis C1704421 Skin pigmentation disorder HSDN C2984057 Have nausea C2073625 X-ray of chest: pleural effusion HSDN C0030193 Sense of pain C0022373 Disease, jejunal HSDN C1384666 Decreased hearing C0282577 Congenital disorders of glycosylation MalaCards C0242936 Center pain C0032372 Poliomyelitis, anterior, acute HSDN C0267596 Bleeding rectal C1959582 Pten hamartoma tumor syndrome MalaCards C0016199 Pain flank C1266044 Collecting duct carcinoma of the kidney UMLS C4084773 Bothered by weight gain C0032019 Pituitary neoplasms HSDN C2919142 Short stature adverse event C1968782 Myopathy, congenital, with excess of muscle spindles MalaCards|HPO C0001825 Agraphia C0012746 Dissociative disorder HSDN C2984058 Have pain C0011253 Delusions HSDN C0009806 Constipate C0026266 Mitral valve insufficiency HSDN C0036572 Convulsion C3280203 Warburg micro syndrome 3 MalaCards|UMLS C1963281 Vomiting adverse event C0341106 Eosinophilic esophagitis MalaCards|HSDN C0030552 Paralysis partial C0007273 Carotid artery diseases HSDN C4084784 Diarrhea C0029877 Ear inflammation HSDN C0015672 Decreased energy C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0221232 Welts C0398775 Hereditary c1 esterase inhibitor deficiency - deficient factor UMLS C0031911 Pigment deposition C1266005 Basaloid squamous cell carcinoma MalaCards C4084768 Usual severity vomiting C1829813 Malonic acidemia MalaCards C0018772 Deafness C1704436 Peripheral arterial diseases HSDN C0018777 Deafness, conductive C0376527 Neoplasm, skull base HSDN C0026821 Cramp C0006325 Bruxism HSDN C0151686 Growth retardation C2931646 Oculocerebral hypopigmentation syndrome type preus MalaCards C0237849 Skin desquamation C0153246 Tinea manus DiseaseOntology|MalaCards C4084768 Usual severity vomiting C0333355 Inflammatory disease of mucous membrane HSDN C0013604 Edematous C0027765 Nervous system disorder HSDN C0011206 Delirium acute C0004238 Atrial fibrillation HSDN C0030552 Paralysis partial C0853697 Neutrophil count decreased HSDN C0013404 Respiratory difficulty C0037120 Pneumonia, nitrogen dioxide HSDN C0557874 Global developmental delay C0268247 Niemann-pick disease, type d MalaCards|HPO C0014089 Functional encopresis C0349231 Phobic anxiety disorder HSDN C0221166 Paraparesis C0752140 Intracranial embolism HSDN C2024878 Cardiovascular surgery result: dyspnea C0017531 Angiolymphoid hyperplasia HSDN C1963091 Diarrhea adverse event C0015408 Eye injury HSDN C0020673 Hypothermia (central) (local) C0018133 Graft-vs-host disease HSDN C0000727 Abdomen acute C4084909 Depression subordinate domain HSDN C0018784 Deafness sensorineural C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C4084802 Usual severity diarrhea C1959626 Mevalonic aciduria MalaCards|HPO C0018772 Deafness C0432313 Epidermolysis bullosa simplex with hypodontia MalaCards C3244654 Sore throat brand of benzocaine & menthol C0018572 Hand, foot and mouth disease DiseaseOntology|MalaCards C0009806 Constipate C0037036 Sialorrhea HSDN C0004604 Pain back C0033860 Psoriasis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0027149 Myxoma HSDN C0040822 D tremors C0206083 Myelinoclasis, central pontine HSDN C1963281 Vomiting adverse event C0812393 Cancer patients and suicide and depression HSDN C0004134 Dyssynergia C1720777 Functional laterality HSDN C3463815 Feel fatigue C0340951 Erythrogenesis imperfecta MalaCards C0242936 Center pain C0040761 Transposition of great vessels HSDN C0042571 Vertigo subjective C0271270 Oculovestibuloauditory syndrome MalaCards C0013604 Edematous C0600260 Lung diseases, obstructive HSDN C0518090 Frequency of pain question C0006433 Burnout, professional HSDN C0030232 Color loss C1567741 Alport syndrome OrphaNet C0022408 Disorder joint C0242217 Calcium pyrophosphate dihydrate deposition MalaCards C3665347 Vision impaired C1856689 Friedreich ataxia 1 HPO C4084773 Bothered by weight gain C0005779 Blood coagulation disorders HSDN C0001825 Agraphia C0017494 Angular gyrus syndrome DiseaseOntology|MalaCards C0018681 Headache, cephalalgia C0221056 Adult type dermatomyositis HSDN C0518090 Frequency of pain question C0031350 Pharyngitis HSDN C0011991 Loose stools C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C3539891 Pelvic pain to the rear C0038941 Incisional infection HSDN C0013604 Edematous C0023772 Lipid metabolism, inborn errors HSDN C4084773 Bothered by weight gain C0043352 Xerostomia HSDN C0008031 Pain chest C0004099 Asthma, exercise-induced HSDN C0039070 Collapse fleeting C3160720 Cardiomyopathy, dilated, 1u MalaCards|HPO|UMLS C2032396 Pelvic pain on the right C0042373 Vascular diseases HSDN C4084724 Usual severity constipation C0030528 Paratyphoid fever DiseaseOntology|MalaCards C0587047 Mass of trunk C0340548 Pulmonary capillary hemangiomatosis UMLS C4085210 Usual severity pain C0018133 Graft-vs-host disease HSDN C4085211 Pain distress question C0019554 Dislocate hip HSDN C2237041 Shox gene with short stature C0432254 Singleton merten syndrome HPO C0178417 Anhedonia C0453996 Tobacco smoking HSDN C0012833 Dizzy C0344315 Depressed mood HSDN C1963091 Diarrhea adverse event C0031117 Peripheral neuropathy HSDN C0424755 Fever symptoms C0016397 Focal infection HSDN C2984058 Have pain C0014548 Epilepsy, generalized HSDN C1963137 Hydrocephalus adverse event C1266184 Atypical teratoid/rhabdoid tumor MalaCards C1313921 Urinomas C0010709 Cyst HSDN C0030193 Sense of pain C0238417 Scorpion sting HSDN C0030554 Abnormal sensation C0010356 Cross infection HSDN C0013421 Dystonia C0949664 Tauopathies HSDN C0014591 Bleeding nose C0042470 Guanarito haemorrhagic fever MalaCards C4085210 Usual severity pain C0037054 Sickle cell trait MalaCards|HSDN C0027498 Nausea vomiting C3280352 Hydatidiform mole, recurrent, 2 MalaCards C2198882 Disturbing or unusual thoughts, feelings, or sensations C0747249 Paranoid ideation UMLS C4084726 Distress cough C0037397 Behavior social HSDN C4085222 Nausea C0518449 Control of hip fracture risk HSDN C0242936 Center pain C0035235 Respiratory syncytial virus infections HSDN C0235108 Tenseness C0233494 Tension UMLS C4085317 Diarrhea frequency C0012147 Dientamoebiases DiseaseOntology C4084802 Usual severity diarrhea C0600104 Obsessive compulsive behavior HSDN C2919142 Short stature adverse event C0268579 Propionic acidemia HPO C0020615 Hypoglycemia nos C0016756 Fructose-1,6-diphosphatase deficiency MalaCards|HPO C0034933 Abnormal reflexes C0022658 Kidney diseases HSDN C0043094 Weight gain C0031117 Peripheral neuropathy HSDN C0018808 Murmur C2931787 Intracardiac myxoma MalaCards C0013404 Respiratory difficulty C0013295 Duodenal ulcer HSDN C3887638 Failure to thrive in infant C1863844 Adult-onset citrullinemia type 2 MalaCards C0018772 Deafness C1848519 Waardenburg syndrome, type 4a OrphaNet|HPO|MalaCards C0151740 Intracranial hypertension C0917890 Pineocytoma OrphaNet|MalaCards C0398650 Idiopathic thrombocytopenia purpura C0037286 Skin neoplasms HSDN C1961131 Cough adverse event C3489393 Hiatal hernia HSDN C4084766 Vomiting C0020502 Hyperparathyroidism HSDN C0013911 Emaciate C0014179 Endometritis HSDN C0026884 Muteness C0024630 Malingering HSDN C0241137 Skin pallor C0086774 Cold hemoglobinuria MalaCards C0151889 Reflexes tendon increased C0004943 Behcet syndrome MalaCards|HPO C0518090 Frequency of pain question C0524988 Schnitzler syndrome HSDN C0030975 Disorders perception C3813607 Infantile gastroesophageal reflux HSDN C4084776 Weight loss C0001883 Airway obstruction HSDN C0035078 Failure kidney C2931783 Amelogenesis imperfecta nephrocalcinosis MalaCards C3539020 Pelvic pain decreasing in frequency C0037929 Spinal cord injuries HSDN C2077894 Masochistic in relationships C0024862 Masochism UMLS C0231791 In toe C1321551 Shprintzen-goldberg syndrome HPO C0030552 Paralysis partial C0037773 Spastic paraplegia, hereditary HSDN C0020903 Illusion C0018592 Joy, festive HSDN C1705500 Flasher - visual manifestation C0346373 Malignant melanoma of iris HPO C2039122 Swollen glands in both sides of neck C0235592 Cervical lymph node large UMLS C3827868 Tachycardia by ecg finding C2931232 Ventricular extrasystoles perodactyly robin sequence MalaCards C0012833 Dizzy C0007789 Cerebral palsy HSDN C0018681 Headache, cephalalgia C0206171 Community acquired infections HSDN C2919142 Short stature adverse event C1291490 Hyaluronidase deficiency OrphaNet|HPO C0013395 Indigestion C0025063 Mediastinal neoplasms HSDN C2919142 Short stature adverse event C1845862 Creatine deficiency, x-linked OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0019285 Diaphragmatic hernia traumatic HSDN C0042571 Vertigo subjective C0155517 Hypoactive labyrinth-unilat. UMLS C0917816 Deficiency mental C0751278 Metachromatic leukodystrophy, infant MalaCards|HPO C4085661 Usual severity nausea C1090821 Sepsis (invertebrate) HSDN C1963087 Constipation adverse event C0026946 Mycoses HSDN C4084775 Usual severity weight loss C0036690 Septicemia HSDN C4084784 Diarrhea C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C0033775 Anal pruritus C1301262 Disorder of anal region UMLS C0042928 Paralysis vocal cord C0087012 Ataxia, spinocerebellar MalaCards|HSDN C3463815 Feel fatigue C0037417 Identification, social HSDN C0028081 Night sweat C1336320 Stage ii hodgkin's disease lymphocyte depletion type below the diaphragm UMLS C4084726 Distress cough C0010709 Cyst HSDN C0032617 High urine output C1527429 Increased blood npn HSDN C0013609 Oedema, localised C0877007 Abdomen edema UMLS C1549543 Administration method - pain C0236733 Amphetamine-related disorders HSDN C4084723 Constipation C0023743 Linitis plastica HSDN C0221232 Welts C0263333 Contact; urticaria UMLS C2315100 Pediatric failure to thrive C1855109 Methylmalonic aciduria cbla type HPO C0151205 Periorbital edema C0340834 Hennekam lymphangiectasia lymphedema syndrome HPO C4085222 Nausea C1623041 Breast-fed HSDN C0027796 Neuralgias C0010709 Cyst HSDN C4085548 Usual severity dizziness C0013990 Pathological accumulation of air in tissues HSDN C1963087 Constipation adverse event C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked HPO C4084776 Weight loss C1384665 Hfe gene HSDN C0042798 Vision dim C4014848 Nanophthalmos 4 MalaCards C4085211 Pain distress question C0002880 Autoimmune hemolytic anemia HSDN C0009398 Color vision defects C0004096 Asthma HSDN C0242936 Center pain C0038187 Starvation HSDN C0522224 Palsied C0795623 Hepatitis a vaccine, inactivated HSDN C1999266 Depression adverse event C1961835 Gaucher disease, type 1 MalaCards C0030200 Intractable pain C0428953 Ecg infarction myocardial HSDN C4084776 Weight loss C0038579 Substance abuse, intravenous HSDN C0042571 Vertigo subjective C0028738 Nystagmus UMLS C0022346 Yellow skin C0019294 Hernia, inguinal HSDN C0004604 Pain back C1690964 Cataract HSDN C0011991 Loose stools C1856143 Hemolytic uremic syndrome, typical MalaCards C0013528 Echo speech C0854912 Pineal germinoma HSDN C0151786 Weakness muscle C0340803 Capillary malformation (disorder) HSDN C2237041 Shox gene with short stature C0024507 Majewski syndrome MalaCards C1963281 Vomiting adverse event C0947622 Cholecystolithiasis HSDN C0018524 Hallucinate C1963280 Vitreous hemorrhage adverse event HSDN C4084724 Usual severity constipation C3854315 Pseudoprimary hyperaldosteronism MalaCards C0277959 Hair coarseness C0917715 Hajdu-cheney syndrome HPO C1963087 Constipation adverse event C1253943 Fluid in the chest HSDN C2919142 Short stature adverse event C1856272 Gonadal dysgenesis, xy type, with associated anomalies OrphaNet|MalaCards C1384666 Decreased hearing C0039494 Temporomandibular joint disorders HSDN C0018784 Deafness sensorineural C0007766 Intracranial aneurysm HSDN C0030193 Sense of pain C0023798 Lipoma HSDN C0575081 Abnormal gait C0268344 Ehlers-danlos syndrome 6b OrphaNet|HPO|MalaCards C0030193 Sense of pain C0009241 Cognition disorders HSDN C0012833 Dizzy C0155520 Labyrinth reactiv.loss-bilat. UMLS C0917816 Deficiency mental C1848392 Zunich neuroectodermal syndrome HPO C4084724 Usual severity constipation C2711227 Steatohepatitis HSDN C0024031 Back pain lower back C0001828 Agricultural workers' diseases HSDN C0034124 Pupillary disorder C0032019 Pituitary neoplasms HSDN C0027497 Queasy C0021818 Intervertebral disk displacement HSDN C2911645 Weight loss adverse event C0206172 Diabetic foot HSDN C4084769 Vomiting frequency C0338437 Neurocysticercosis HSDN C0040822 D tremors C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C0206160 Retic count elevated C1969106 Osteopetrosis, autosomal recessive 4 MalaCards|HPO C0036396 Sciatica C0037929 Spinal cord injuries HSDN C0036572 Convulsion C0024314 Lymphoproliferative disorders HSDN C4084775 Usual severity weight loss C2749484 Neuroblastoma, susceptibility to HPO C0009806 Constipate C2748910 Rett syndrome, atypical MalaCards|HPO C0020458 Hyperhydrosis C0036472 Scrub typhus OrphaNet|MalaCards C4084776 Weight loss C0030805 Bullous pemphigoid OrphaNet|HPO|MalaCards C1963067 Atrial fibrillation adverse event C3554194 Chtd3 MalaCards C1963091 Diarrhea adverse event C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0000737 Abdomen pain C0085298 Sudden cardiac death HSDN C2203646 Jaundice C0008325 Cholecystitis HPO C2984058 Have pain C0041755 Adverse reaction to drug HSDN C0030193 Sense of pain C1868649 Panic disorder 1 HSDN C0237326 Defecation pain C1838569 Caudal dysgenesis syndrome HPO C1000483 Genus anemia C1858583 Hemosiderosis, systemic, due to aceruloplasminemia HPO C0518090 Frequency of pain question C0026916 Mycobacterium avium-intracellulare infection HSDN C0036572 Convulsion C4014488 Pontocerebellar hypoplasia, type 2e MalaCards|UMLS C0041105 Jaw spasm C0161406 Injury nerve trigeminal HSDN C0042928 Paralysis vocal cord C0009946 Conversion disorder HSDN C1546759 Specimen source codes - pustule C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C0262384 Chest pain atypical C1456822 Claudication (finding) UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C0005779 Blood coagulation disorders HSDN C1579931 Depressed - symptom C1970035 Parkinson disease 6, late-onset, susceptibility to HPO C3665347 Vision impaired C0242383 Age related macular degeneration MalaCards C0011570 Monopolar depression C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C1279888 Proteinuria of undiagnosed cause C0878681 Dent's disease OrphaNet C1510456 Wernicke aphasia C0751795 Head injury penetrating HSDN C0151825 Ostalgia C2020284 Stickler syndrome, type 1 MalaCards C0000737 Abdomen pain C3809369 Paroxysmal nocturnal hemoglobinuria 2 MalaCards|UMLS C0231712 Gait waddling C0432215 Progressive pseudorheumatoid dysplasia HPO|UMLS C1963093 Dizziness adverse event C0008066 Child behavior disorders HSDN C1963086 Confusion adverse event C0220847 C hepatitis virus HSDN C0860603 Anxiety symptom C1864100 Pseudohypoparathyroidism, type ib MalaCards|HPO C0010200 Cough symptom C0018916 Hemangioma HSDN C0035229 Respiratory function impaired C1859591 Aural atresia, multiple congenital anomalies, and mental retardation OrphaNet|MalaCards C0232466 Feeding difficulty C1864171 Peroxisome biogenesis disorder, complementation group 12 MalaCards C0917816 Deficiency mental C0027877 Neuronal ceroid-lipofuscinoses OrphaNet|MalaCards C4084766 Vomiting C3150679 Eoe2 MalaCards C0018772 Deafness C0524801 Retinal neoplasms HSDN C0151311 Cranial nerve palsy C0015625 Fanconi anemia MalaCards|HPO C1963093 Dizziness adverse event C0026764 Multiple myeloma HSDN C4084769 Vomiting frequency C0026946 Mycoses HSDN C0018926 Emesis bloody C3203359 Rupture HSDN C0151889 Reflexes tendon increased C0265329 Organoid nevus phakomatosis OrphaNet|HPO C3541349 Syncope C0595812 Fistula route HSDN C0011168 Disorder deglutition C0796176 Stuve-wiedemann syndrome HPO C1557397 Adverse event associated with pain C0221752 Rbc urine HSDN C3829611 Nausea frequency C0018916 Hemangioma HSDN C1279888 Proteinuria of undiagnosed cause C0011303 Demyelinating diseases HSDN C0086437 Joint hypermobility C0432242 Desbuquois syndrome MalaCards|HPO C4084723 Constipation C0033246 Proctitis HSDN C0018991 Paralysis one side of body C0021400 Influenza HSDN C2364111 Gustatory anesthesia C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating HSDN C0042963 Symptoms vomiting C0042216 Poxvirus officinalis HSDN C0030193 Sense of pain C0030920 Peptic ulcer HSDN C0751837 Gait ataxic C0266463 Lissencephaly HSDN C3665492 Pigmentations C0009402 Colorectal carcinoma MalaCards C2911645 Weight loss adverse event C0041755 Adverse reaction to drug HSDN C4085211 Pain distress question C0033999 Pterygium HSDN C4084726 Distress cough C0019829 Hodgkin disease OrphaNet C0015468 Face pain C0033324 Prognathism HSDN C2911645 Weight loss adverse event C0032285 Pneumonia HSDN C0009806 Constipate C0007873 Uterine cervical neoplasm HSDN C0020455 Hypergammaglobulinemia C0007137 Squamous cell carcinoma HSDN C0242670 Chronic vegetative state C3810814 Myocardial infarction ecg assessment HSDN C0015672 Decreased energy C1546635 Specimen source codes - fistula HSDN C1963071 Back pain adverse event C0015467 Neuralgia facial HSDN C0030193 Sense of pain C0038271 Stereotyped behavior HSDN C0518090 Frequency of pain question C0002382 Alveolar bone loss HSDN C4084788 Have dizziness C0025284 Meningeal neoplasms HSDN C0232466 Feeding difficulty C2675875 Chromosome 2p16.1 p15 deletion syndrome MalaCards C0036572 Convulsion C1565489 Renal insufficiency HSDN C0235014 Fontanel bulging C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|UMLS C2984058 Have pain C0007868 Cervical dysplasia HSDN C4084773 Bothered by weight gain C0009395 Color perception HSDN C0013421 Dystonia C0017601 Glaucomas HSDN C2024893 Cardiovascular surgery result: fatigue C0015695 Fatty liver HSDN C4084726 Distress cough C0206255 Malaria vaccine HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017919 Glycogen storage disease HSDN C2919142 Short stature adverse event C0265202 Seckel syndrome OrphaNet|HPO|MalaCards C1962976 Ventricular fibrillation adverse event C3150953 Long qt syndrome 6 MalaCards|HPO C0024031 Back pain lower back C0013289 Duodenal diseases HSDN C0026838 Spasticity muscle C0024141 Lupus erythematosus, systemic HSDN C2237041 Shox gene with short stature C3150880 Chromosome 17q23.1-q23.2 duplication syndrome MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007350 Cat disease HSDN C0413252 Hypothermia due to exposure C0006309 Brucellosis HSDN C0518090 Frequency of pain question C0023290 Leishmaniasis, visceral HSDN C0019209 Large liver C0024445 Lipomatosis, familial benign cervical OrphaNet|HPO|MalaCards C0242936 Center pain C0004576 Babesiosis HSDN C3494358 Characteristic, prodromal C2936631 Complaint, subjective health HSDN C0003862 Pain joint C0018995 Hemochromatosis OrphaNet C2984058 Have pain C0677866 Brain stem neoplasms HSDN C4085222 Nausea C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C4085211 Pain distress question C0035008 Reinforcement schedules HSDN C0237326 Defecation pain C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0085423 Gram-negative bacterial infections HSDN C0042963 Symptoms vomiting C1546635 Specimen source codes - fistula HSDN C0015672 Decreased energy C0302280 Adrenogenital syndrome HSDN C0013528 Echo speech C0265249 Mietens' syndrome MalaCards C0020455 Hypergammaglobulinemia C0027947 Neutropenia HSDN C3274924 Have been coughing C0032226 Pleural diseases HSDN C0232466 Feeding difficulty C3810055 Combined oxidative phosphorylation deficiency 19 MalaCards C4084768 Usual severity vomiting C2673477 Hypophosphatasia, perinatal lethal MalaCards|HPO C3463815 Feel fatigue C0752352 Muscular disorders, atrophic HSDN C0016204 Fart C0025472 Mesenteric vascular occlusion HSDN C4084802 Usual severity diarrhea C0242216 Biliary calculi HSDN C4084769 Vomiting frequency C0013274 Patent ductus arteriosus HSDN C4085317 Diarrhea frequency C2936350 Plaque, atherosclerotic HSDN C4084788 Have dizziness C0041296 Tuberculosis HSDN C0236000 Jaw bone pain C1704981 Hyperparathyroidism-jaw tumor syndrome HPO C0002170 Alopecia disorders C1855789 Self-healing collodion baby MalaCards|HPO C3898969 Have been vomiting C0344434 Atrial fibrillation ecg HSDN C4084767 Bothered by vomiting C0062527 Hepatitis b vaccine HSDN C4084724 Usual severity constipation C0031873 Pica disease HSDN C1145670 Failure respiratory C3489730 Alveolar hypoventilation syndrome MalaCards C0026838 Spasticity muscle C3887662 Intraspinal neoplasm HSDN C0086439 Activity decreased C0472377 Basal ganglia hemorrhage HSDN C4085210 Usual severity pain C0206655 Alveolar rhabdomyosarcoma HSDN C2984058 Have pain C0027927 Neurosyphilis HSDN C0557874 Global developmental delay C3891452 Seckel syndrome 8 MalaCards C0013362 Dysarthrias C1855396 Alpha mannosidosis, type ii HPO C4084769 Vomiting frequency C1833511 Carnitine palmitoyltransferase ii deficiency, infantile HPO C0700590 Diaphoresis excessive C4053907 Early onset tylosis MalaCards C3178766 Nociceptive pain C0282488 Interstitial cystitis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0002453 Amenorrhea HSDN C1961131 Cough adverse event C1956390 Cranial arteritis MalaCards C0087169 Withdrawal symptoms C0452201 Withdr symp,ther use drug newb UMLS C0011206 Delirium acute C0024299 Lymphoma HSDN C0003962 Ascites C3888317 Sialidosis, type 2 OrphaNet C0426579 Anorexia symptom C0017185 Gastrointestinal neoplasms HSDN C1142414 Sensation of pressure in eye C0948595 Ocular discomfort UMLS C1963091 Diarrhea adverse event C0001418 Adenocarcinoma HSDN C0597925 Mobile spasm C0392702 Abnormal involuntary movement UMLS C0009676 Confusion state C0349464 Wernicke-korsakoff syndrome MalaCards C1963063 Anorexia adverse event C0018249 Grooming HSDN C0020673 Hypothermia (central) (local) C0013870 Electroconvulsive shock HSDN C0023530 Leukopenia C1848578 Methylmalonic aciduria and homocystinuria, cblf type (disorder) MalaCards|HPO C0424755 Fever symptoms C0003851 Arteriosclerosis obliterans HSDN C0151786 Weakness muscle C0027859 Acoustic neuroma HSDN C0030486 Extremity paralysis, lower C0020615 Hypoglycemia HSDN C0014089 Functional encopresis C0162818 Skin diseases, papulosquamous HSDN C0032617 High urine output C3827868 Tachycardia by ecg finding HSDN C0030193 Sense of pain C0021295 Infant, premature, diseases HSDN C1971624 Appetite absent C0039841 Thiamine deficiency HSDN C0015469 Facial paralysis C3887654 Polyarteritis nodosa, childhood-onset MalaCards C2029884 Hearing loss by exam C0037304 Skull fracture HSDN C0231218 Malaise generalized C1336248 Hepatocellular cancer stage iii ajcc v6 UMLS C0015230 Exanthem C0029291 Fever, parrot DiseaseOntology|MalaCards C4085548 Usual severity dizziness C0018939 Hematological disease HSDN C0349588 Stature short C3151113 Meier-gorlin syndrome 3 MalaCards C0349588 Stature short C0206641 Osteochondromatosis OrphaNet|HPO C0349489 Fetal hypoxia C0152156 Dystocia HSDN C0015672 Decreased energy C0027126 Myotonic dystrophy HSDN C4084784 Diarrhea C0020619 Hypogonadism HSDN C1565249 Limitation, mobility C0037939 Spinal neoplasms HSDN C0024312 Lymphocytopenia C1851970 Dyskeratosis congenita, autosomal dominant MalaCards|HPO C0270948 Neurogenic muscular atrophy C0036161 Sandhoff disease HPO C0034150 Skin purpura C1527429 Increased blood npn HSDN C0009421 Comatose C0032001 Pituitary apoplexy MalaCards|HSDN C0033790 Pseudobulbar palsy C0022336 Creutzfeldt-jakob disease HSDN C0002965 Crescendo angina C0042029 Urinary tract infection HSDN C1527344 Dysphonia C0752353 Atrophy, muscular, spinobulbar OrphaNet|HPO C1963281 Vomiting adverse event C0085693 Acute appendicitis nos (disorder) MalaCards C1860844 Sparse, thin hair C0432269 Lenz majewski hyperostotic dwarfism MalaCards|HPO C2919142 Short stature adverse event C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C4084774 Have weight loss C0023441 Leukemia, experimental HSDN C0010038 Corneal opacity disorder C3805432 Cob1 MalaCards C4084774 Have weight loss C0009475 Community mental health service HSDN C0151786 Weakness muscle C3178801 Stroke, lacunar HSDN C0009806 Constipate C2315264 Constipation due to spasm of colon UMLS C0085631 Abnormal excitement C0796121 Primrose syndrome MalaCards C0518090 Frequency of pain question C0206762 Limb deformities, congenital HSDN C0030486 Extremity paralysis, lower C0042021 Urinary fistula HSDN C0518090 Frequency of pain question C0024961 Injuries maxillofacial HSDN C0018772 Deafness C0037355 Smallpox vaccines HSDN C2242996 Tingling C0034040 Puerperal disorders HSDN C4084767 Bothered by vomiting C0028768 Obsessive-compulsive disorder HSDN C2984058 Have pain C0001849 Aids dementia complex HSDN C4042891 Sleep wake disorders C0003873 Rheumatoid arthritis HSDN C0008031 Pain chest C1579931 Depressed - symptom HSDN C3641756 Have diarrhea C0007020 Carbon monoxide poisoning HSDN C0019572 Hairiness C2675861 Lipodystrophy, congenital generalized, type 3 MalaCards|HPO C1145670 Failure respiratory C0751267 Encephalopathy, subacute necrotizing, infantile OrphaNet|MalaCards C0007758 Cerebellar ataxia C0014549 Tonic-clonic epilepsy HSDN C0000737 Abdomen pain C3897082 Stage iva colon cancer UMLS C4084773 Bothered by weight gain C0034089 Pulmonary valve stenosis HSDN C0004134 Dyssynergia C0238286 Mucolipidosis type iv OrphaNet|HPO|MalaCards C1963252 Tremor adverse event C0238052 Xanthomatosis, cerebrotendinous OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C1090821 Sepsis (invertebrate) HSDN C0034933 Abnormal reflexes C0243026 Sepsis HSDN C0332573 Macula C0038325 Stevens-johnson syndrome OrphaNet|HPO C1963086 Confusion adverse event C0016658 Fracture bone HSDN C1963093 Dizziness adverse event C0006840 Candidiasis HSDN C2037136 Sudden loss of vision in temporal half of visual fields in both eyes C0271202 Hemianopsia homonymous UMLS C0030193 Sense of pain C1511316 Breast large cell neuroendocrine carcinoma UMLS C0042798 Vision dim C1999266 Depression adverse event HSDN C4084766 Vomiting C0022116 Ischemia HSDN C0575081 Abnormal gait C1868675 Parkinson disease 2, autosomal recessive juvenile HPO C3812171 Bradycardia by ecg finding C0281479 Primary systemic amyloidosis MalaCards C0027498 Nausea vomiting C0031069 Familial mediterranean fever OrphaNet|HPO C0030193 Sense of pain C0042749 Viremia HSDN C0043094 Weight gain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0700078 Deep tendon reflex decrease C3550693 Peroxisome biogenesis disorder 3b MalaCards|UMLS C0393754 Headache associated with sexual activity C0809993 Headache; including migraine UMLS C4084774 Have weight loss C0037661 Somatostatinoma OrphaNet|MalaCards C2242996 Tingling C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C0037763 Spasm C0019348 Herpes simplex infections HSDN C4084769 Vomiting frequency C0027627 Neoplasm metastasis HSDN C2024893 Cardiovascular surgery result: fatigue C0043528 Zoonoses HSDN C2024893 Cardiovascular surgery result: fatigue C0017574 Gingivitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0242855 Congenital atresia of pulmonary valve HSDN C0018524 Hallucinate C0270611 Brain damage HSDN C0917816 Deficiency mental C3809738 Alacrima, achalasia, and mental retardation syndrome MalaCards C3641755 Have constipation C0242343 Panhypopituitarism MalaCards|HPO C0020672 Body temperature decreased C1552527 Clinic / center - developmental disabilities HSDN C1963281 Vomiting adverse event C0079774 Peripheral t-cell lymphoma HSDN C4084767 Bothered by vomiting C0002991 Cutaneous fibrous histiocytoma HSDN C0030552 Paralysis partial C0747533 Peroneal neuropathy HSDN C0018772 Deafness C0796062 Microcephaly-deafness syndrome MalaCards C4084773 Bothered by weight gain C0001249 Actinobacillus infections HSDN C1963087 Constipation adverse event C0019326 Ventral hernia HSDN C2237041 Shox gene with short stature C0342649 Vascular calcification MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0018789 Cardiac aneurysm HSDN C3641756 Have diarrhea C0039103 Synovitis HSDN C0018991 Paralysis one side of body C0038186 Reflex, startle HSDN C3887784 Decreased urine output C2239253 Aneurysm of sinus of valsalva MalaCards C3541349 Syncope C0474820 Glomerocytoma tympanicum HSDN C0041657 Consciousness loss C1962958 Hematoma adverse event HSDN C0008031 Pain chest C1762616 Meningioma, benign, no icd-o subtype HSDN C0398650 Idiopathic thrombocytopenia purpura C0024530 Malaria HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017605 Angle closure glaucoma HSDN C0009421 Comatose C0162557 Liver failure, acute HSDN C4084769 Vomiting frequency C0023176 Lead poisoning MalaCards C0231528 Muscle pain generalized C0221011 Malignant atrophic papulosis HSDN C0026838 Spasticity muscle C1862941 Amyotrophic lateral sclerosis, sporadic HPO C4085661 Usual severity nausea C0344434 Atrial fibrillation ecg HSDN C0233565 Bradykinesia C3149705 Parkinson disease 1, autosomal dominant lewy body HPO C4085862 Bothered by nausea C0004238 Atrial fibrillation HSDN C0151786 Weakness muscle C0027746 Nerve degeneration HSDN C0041105 Jaw spasm C1881674 Medical device emits smoke HSDN C0033774 Skin pruritus C2980107 Prurigo, hebra's UMLS C0042963 Symptoms vomiting C0346378 Ciliary body medulloepithelioma UMLS C1963065 Apnea adverse event C0265211 Marshall-smith syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0342443 Adrenal cushing's syndrome MalaCards|HSDN C4085548 Usual severity dizziness C0018213 Graves disease HSDN C1963091 Diarrhea adverse event C0276932 Schistosoma; intercalatum DiseaseOntology C0030193 Sense of pain C0019348 Herpes simplex infections HSDN C1963086 Confusion adverse event C0024121 Lung neoplasms HSDN C0413252 Hypothermia due to exposure C0236969 Substance-related disorders HSDN C1549543 Administration method - pain C0016397 Focal infection HSDN C0013404 Respiratory difficulty C1861984 Cardiac conduction defect, nonprogressive HPO C0242936 Center pain C0021841 Intestinal neoplasms HSDN C1962972 Proteinuria adverse event C0007621 Neoplastic cell transformation HSDN C1579931 Depressed - symptom C0878682 Ceruloplasmin deficiency OrphaNet|HPO|MalaCards C0040264 Ear ringing sound C0086045 Concentration HSDN C4085549 Dizziness C3541306 Plasmodium measurement HSDN C0027424 Congestion nasal C0810022 Other upper respiratory disease UMLS C0042420 Vasovagal episode C0026267 Mitral valve prolapse syndrome HSDN C4084727 Cough frequency C0033860 Psoriasis HSDN C0860603 Anxiety symptom C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C1963184 Nystagmus adverse event C1845407 Cone-rod dystrophy, x-linked, 3 HPO C0024031 Back pain lower back C0023176 Lead poisoning HSDN C0008031 Pain chest C1710499 Type iii pleuropulmonary blastoma UMLS C0013404 Respiratory difficulty C0340543 Familial primary pulmonary hypertension HSDN C3829611 Nausea frequency C0015934 Fetal growth retardation HSDN C4085211 Pain distress question C0243013 Base learn problems HSDN C0033774 Skin pruritus C0008049 Chicken pox HSDN C3494358 Characteristic, prodromal C0751871 Autoimmune diseases of the nervous system HSDN C4084768 Usual severity vomiting C0969753 Nidovirales infections HSDN C0030193 Sense of pain C4049867 Giant cell lesion of small bones UMLS C4084767 Bothered by vomiting C0037937 Spine injury HSDN C0000737 Abdomen pain C0030793 Pelvis tumor HSDN C3463815 Feel fatigue C0085409 Polyendocrinopathies, autoimmune HSDN C0851578 Disorder sleep C0017658 Glomerulonephritis HSDN C0036572 Convulsion C0751667 Canavan disease, juvenile MalaCards C0042963 Symptoms vomiting C0013922 Embolism HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036346 Schizophrenia, childhood HSDN C4084775 Usual severity weight loss C0043048 Experimental water deprivation HSDN C0042384 Vasculitis, nonspecific C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0026918 Mycobacterium infections HSDN C0030193 Sense of pain C0025500 Mesothelioma HSDN C4084802 Usual severity diarrhea C0023240 Legionellosis MalaCards C1963252 Tremor adverse event C0039336 Gustatory sense HSDN C1384666 Decreased hearing C2984291 Glioblastoma multiforme pathway HSDN C0023012 Delay language C1866504 Photosensitive trichothiodystrophy MalaCards C0151889 Reflexes tendon increased C0795889 Allan-herndon-dudley syndrome (ahds) OrphaNet|HPO|MalaCards C0314719 Dry eyes C0014805 Primary erythermalgia MalaCards|UMLS C4084727 Cough frequency C0001486 Adenovirus infections HSDN C3829611 Nausea frequency C1962983 Cataract adverse event HSDN C0233514 Behavior abnormal C1862682 Aortic arch anomaly with peculiar facies and mental retardation MalaCards C2096293 Ent surgical result ear vertigo C0022701 Kinesthesia HSDN C2203646 Jaundice C0085183 Neoplasms, second primary HSDN C0024902 Mastodynia C0037047 Sibling HSDN C0349588 Stature short C0265449 Pallister-killian syndrome OrphaNet|MalaCards C0522224 Palsied C0013922 Embolism HSDN C0086437 Joint hypermobility C1844887 Catel manzke syndrome MalaCards|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0014358 Enterocolitis, pseudomembranous HSDN C0043094 Weight gain C0035242 Respiratory tract diseases HSDN C2911647 Weight gain adverse event C0042029 Urinary tract infection HSDN C0042510 Fibrillation paroxysmal vent C3150956 Long qt syndrome 5, acquired, susceptibility to HPO C0042964 Anticipatory vomiting C0919267 Ovarian neoplasm HSDN C3641756 Have diarrhea C0032787 Postoperative complications HSDN C1962972 Proteinuria adverse event C0002382 Alveolar bone loss HSDN C3641756 Have diarrhea C0003855 Arteriovenous fistula HSDN C4085661 Usual severity nausea C0037939 Spinal neoplasms HSDN C1963091 Diarrhea adverse event C0024620 Primary malignant neoplasm of liver MalaCards C0042024 Urine incontinence C0162871 Aortic aneurysm, abdominal HSDN C0686770 Leser-trelat sign C1882062 Neoplastic disease UMLS C0000737 Abdomen pain C0085435 Arthritis, reactive OrphaNet|MalaCards C4085210 Usual severity pain C0242659 Female homosexual HSDN C0751409 Upper extremity weakness C2939419 Cancer metastatic UMLS C0151889 Reflexes tendon increased C1849678 Peroxisomal acyl-coa oxidase deficiency OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C2717757 Retinocochleocerebral vasculopathies MalaCards C0020672 Body temperature decreased C0036341 Schizophrenia HSDN C4084768 Usual severity vomiting C0005944 Metabolic bone disorder HSDN C0026826 High muscle tone C2931585 Gaucher-like disease OrphaNet|HPO|MalaCards C0011991 Loose stools C0026936 Mycoplasma infections HSDN C0018681 Headache, cephalalgia C0343115 Skin mastocytoma MalaCards|HPO C0013404 Respiratory difficulty C0023860 Listeriosis HSDN C0034933 Abnormal reflexes C0027821 Syndrome effort HSDN C0042420 Vasovagal episode C0003873 Rheumatoid arthritis HSDN C0024031 Back pain lower back C0038454 Cerebrovascular accident HSDN C0018772 Deafness C0079772 T-cell lymphoma HSDN C0004134 Dyssynergia C1858712 Spastic paraplegia 10, autosomal dominant MalaCards|HPO C0026826 High muscle tone C1865208 Anal atresia, hypospadias, and penoscrotal inversion MalaCards C2029884 Hearing loss by exam C1556682 Adverse event associated with infection HSDN C0013362 Dysarthrias C0334511 Pleural solitary fibrous tumor HSDN C0019209 Large liver C1414525 Fah gene HPO C2029884 Hearing loss by exam C1834711 Cerebelloparenchymal disorder vi MalaCards C3463815 Feel fatigue C0013720 Ehlers-danlos syndrome HSDN C0018991 Paralysis one side of body C2937287 Hematolysis HSDN C0018784 Deafness sensorineural C2936331 Sarcoglycanopathies HSDN C0237326 Defecation pain C1845902 Fg syndrome 2 MalaCards|HPO C4084727 Cough frequency C0029408 Degenerative polyarthritis HSDN C2242508 Andropausal symptoms C3495833 Loh syndrome UMLS C0497247 Blood pressure elevation C2674705 Osteolysis, hereditary, of carpal bones with or without nephropathy MalaCards|HPO C0427068 Legs weakness C1847582 Lipodystrophy with congenital cataracts and neurodegeneration HPO C4084726 Distress cough C0026636 Mouth diseases HSDN C0518090 Frequency of pain question C0175754 Agenesis of corpus callosum HSDN C2024893 Cardiovascular surgery result: fatigue C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0242936 Center pain C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C0221151 Vomit projectile C1850053 Pelizaeus-merzbacher-like disease, autosomal recessive, 2 MalaCards|HPO C3463815 Feel fatigue C0038041 Spotted fevers DiseaseOntology|MalaCards C0022346 Yellow skin C0009241 Cognition disorders HSDN C0015230 Exanthem C0524988 Schnitzler syndrome OrphaNet|MalaCards C2984058 Have pain C0376154 Skin callus HSDN C0037199 Sinus infection C0241932 X-linked hypogammaglobulinemia HPO C1963065 Apnea adverse event C0008626 Congenital chromosomal disease HSDN C1836296 Lower extremity weakness C1853247 Spastic paraplegia 31, autosomal dominant MalaCards|HPO|UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0205788 Histiocytoid hemangioma HSDN C0036572 Convulsion C1833473 Dermoid cysts, familial frontonasal MalaCards C4084766 Vomiting C0036864 Sexual relations HSDN C0037763 Spasm C0027073 Myofascial pain syndromes HSDN C4084726 Distress cough C0878555 Diffuse panbronchiolitis MalaCards C0033774 Skin pruritus C0162566 Porphyria cutanea tarda HSDN C0151889 Reflexes tendon increased C0018523 Hallervorden-spatz syndrome OrphaNet|MalaCards C1963184 Nystagmus adverse event C0796147 Acrocallosal syndrome MalaCards|HPO C0349588 Stature short C0085131 Gangliosidosis gm1 OrphaNet|MalaCards C3274924 Have been coughing C0031090 Periodontal diseases HSDN C0037763 Spasm C0042487 Venous thrombosis HSDN C1549543 Administration method - pain C0010034 Corneal diseases HSDN C0007398 Catatonic C2326002 Infradentale HSDN C0040822 D tremors C0349653 Congenital disorder of glycosylation type 1a MalaCards C0007758 Cerebellar ataxia C1665347 Cerebellar ataxia associated with another disorder UMLS C3887638 Failure to thrive in infant C0265706 Gastroschisis HSDN C0746674 Muscle weakness generalized C1861752 Multicore myopathy, moderate, with hand involvement HPO C0033377 Caudal displacement C0265224 Freeman-sheldon syndrome OrphaNet|HPO|MalaCards C1963071 Back pain adverse event C0042769 Virus diseases HSDN C4085210 Usual severity pain C1963211 Pericarditis adverse event HSDN C0040485 Wryneck C0039093 Congenital abnormal synostosis HSDN C0917816 Deficiency mental C3809877 Schaaf-yang syndrome MalaCards C0020455 Hypergammaglobulinemia C0019209 Hepatomegaly HSDN C0026821 Cramp C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0036572 Convulsion C1855128 Methylcobalamin deficiency, cblg type MalaCards|HPO|UMLS C0424755 Fever symptoms C0041313 Hepatic tuberculosis DiseaseOntology|MalaCards C0008031 Pain chest C0023676 Life style HSDN C0150055 Pain chronic C0002957 Anger HSDN C4085552 Dry mouth C0014805 Primary erythermalgia MalaCards C0018991 Paralysis one side of body C0014859 Esophageal neoplasms HSDN C0424755 Fever symptoms C2316212 Cryopyrin-associated periodic syndromes MalaCards C0013604 Edematous C0796113 Nephroblastomatosis, fetal ascites, macrosomia and wilms tumor MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0005695 Bladder neoplasm HSDN C0015469 Facial paralysis C0340427 Familial dilated cardiomyopathy MalaCards C0751495 Seizure focal C0282512 Landau-kleffner syndrome MalaCards C4084773 Bothered by weight gain C0013990 Pathological accumulation of air in tissues HSDN C0030552 Paralysis partial C0221002 Hyperparathyroidism, primary HSDN C4084802 Usual severity diarrhea C0036982 Shock, hemorrhagic HSDN C0019825 Voice hoarseness C1857255 Diastrophic dysplasia, broad bone platyspondylic variant HPO C0349588 Stature short C2678408 Pituitary hormone deficiency, combined, 4 MalaCards C0423517 Blood discharge from ear C0019080 Hemorrhage UMLS C0030193 Sense of pain C0043119 Werner syndrome HSDN C0042963 Symptoms vomiting C0018800 Cardiomegaly HSDN C4084766 Vomiting C1855115 Methylmalonic aciduria, mut(0) type HPO C0002962 Angina C3542024 Aortic valve disease 2 MalaCards C0041105 Jaw spasm C0016508 Congenital foot deformity HSDN C0040034 Thrombocytopenia C0041409 Turner syndrome, male MalaCards C0037771 Paraparesis spastic C1261470 Congenital meningocele HSDN C4084768 Usual severity vomiting C0026782 Mumps vaccine HSDN C0460137 Push down or depress C1852372 Mitochondrial complex iii deficiency (disorder) HPO C1963137 Hydrocephalus adverse event C1531647 Cerebral ventriculomegaly HPO C1963281 Vomiting adverse event C0524620 Metabolic syndrome x HSDN C2203646 Jaundice C0453996 Tobacco smoking HSDN C0454644 Delayed language development C0432442 Chromosome 18p deletion syndrome MalaCards C0010200 Cough symptom C0004153 Atherosclerosis HSDN C0011570 Monopolar depression C0035372 Rett syndrome OrphaNet|HPO|MalaCards C0020505 Excessive eating C0040156 Thyrotoxicosis MalaCards C0039070 Collapse fleeting C0017636 Glioblastoma HSDN C4085211 Pain distress question C0032816 Post-concussion headache HSDN C2032395 Pelvic pain on the left C0458219 Complex regional pain syndromes HSDN C1260880 Nasal drip C0349535 Carcinoid tumor of intestine MalaCards C0027066 Myoclonic jerking C0085209 Bovine spongiform encephalitis MalaCards C4084767 Bothered by vomiting C0018571 Hand injury HSDN C2024893 Cardiovascular surgery result: fatigue C0405580 Adrenal cortical hypofunction HSDN C0231218 Malaise generalized C3899976 Bclc stage d adult hepatocellular carcinoma UMLS C1963071 Back pain adverse event C0040053 Thrombosis HSDN C0042571 Vertigo subjective C0022410 Joint instability HSDN C0004604 Pain back C0393735 Headache disorders HSDN C0000737 Abdomen pain C0005403 Bile reflux HSDN C1557397 Adverse event associated with pain C0162832 Apc HSDN C2024893 Cardiovascular surgery result: fatigue C0242343 Panhypopituitarism OrphaNet|HPO|MalaCards C0557874 Global developmental delay C1859817 2-aminoadipic 2-oxoadipic aciduria HPO C0007758 Cerebellar ataxia C3281223 Canvas UMLS C0030554 Abnormal sensation C0020941 Immersion foot HSDN C4084725 Usual severity cough C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084802 Usual severity diarrhea C0017128 Fistula gastric HSDN C0020580 Decreased sensation C0030581 Parotid neoplasms HSDN C0151786 Weakness muscle C1556682 Adverse event associated with infection HSDN C0030193 Sense of pain C0027664 Neoplasms, muscle tissue HSDN C0011206 Delirium acute C0036421 Systemic scleroderma HSDN C0003862 Pain joint C0040428 Abrasion dental HSDN C0518090 Frequency of pain question C0206655 Alveolar rhabdomyosarcoma HSDN C4085317 Diarrhea frequency C0268322 Chester-type porphyria HPO C2984058 Have pain C1963084 Colitis adverse event HSDN C1549543 Administration method - pain C0014378 Enterovirus infections HSDN C0241210 Speaking delay C1859564 Bardet-biedl syndrome 3 HPO C2024878 Cardiovascular surgery result: dyspnea C3814778 Hemolytic index HSDN C0848203 Male pelvic pain C0010068 Coronary heart disease HSDN C0684343 Pseudophakia C0013581 Ectopia lentis HSDN C3539889 Pelvic pain increasing in severity C0001418 Adenocarcinoma HSDN C0349588 Stature short C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C0151825 Ostalgia C0278724 Ds stage iii plasma cell myeloma UMLS C4084775 Usual severity weight loss C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0009806 Constipate C2609414 Acute kidney injury HSDN C0034150 Skin purpura C0026769 Multiple sclerosis HSDN C0002622 Amnesias C0314657 Genetic predisposition HSDN C0155552 Hearing loss mixed C1510455 Acrocephalosyndactylia HSDN C0037315 Breathing disorder during sleeping C3554774 Tyshchenko syndrome MalaCards C0030486 Extremity paralysis, lower C1556682 Adverse event associated with infection HSDN C4084802 Usual severity diarrhea C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C0018777 Deafness, conductive C1844696 Otopalatodigital syndrome, type ii MalaCards|HPO C4042891 Sleep wake disorders C0220981 Metabolic acidosis HSDN C0917801 Sleep disorder insomnia C1561839 Drug induced insomnia UMLS C1962972 Proteinuria adverse event C1704436 Peripheral arterial diseases HSDN C0013404 Respiratory difficulty C0031049 Tuberculous pericarditis HSDN C0398650 Idiopathic thrombocytopenia purpura C0003864 Arthritis HSDN C0020580 Decreased sensation C0009492 Compartment syndromes HSDN C0012833 Dizzy C0013295 Duodenal ulcer HSDN C2936229 Idiopathic apparent life threatening event C0752308 Hypoxia-ischemia, brain HSDN C0518090 Frequency of pain question C0085092 Parenting behavior HSDN C1963252 Tremor adverse event C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0005745 Blepharoptosis C1837122 Myasthenic syndrome, congenital, fast-channel MalaCards|HPO C0557874 Global developmental delay C0796004 Kabuki make-up syndrome MalaCards|HPO C0271215 Blindness legal C1833872 Ophthalmomandibulomelic dysplasia OrphaNet|MalaCards C0522224 Palsied C2706915 Language:-:point in time:^patient:- HSDN C4085210 Usual severity pain C0029132 Disorder of the optic nerve HSDN C2711646 Alexia and agraphia present C0002018 Alexia UMLS C0030554 Abnormal sensation C0018790 Cardiac arrest HSDN C1384666 Decreased hearing C0149514 Bronchitis acute HSDN C0000786 Abortion spontaneous C0040028 Thrombocythemia, essential MalaCards C1145670 Failure respiratory C0265220 Pallister-hall syndrome MalaCards C0023380 Lethargy C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C0018681 Headache, cephalalgia C0027663 Neoplasms, multiple primary HSDN C1963086 Confusion adverse event C0035435 Rheumatism HSDN C0009806 Constipate C0023892 Biliary cirrhosis HSDN C1549543 Administration method - pain C0024473 Magnesium deficiency HSDN C1549543 Administration method - pain C0149925 Small cell carcinoma of lung HSDN C0917816 Deficiency mental C1856796 Estren-dameshek variant of fanconi anemia HPO C4085210 Usual severity pain C0015625 Fanconi anemia HSDN C4085211 Pain distress question C0017563 Gingival diseases HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0017178 Gastrointestinal diseases HSDN C1963281 Vomiting adverse event C0026953 Mycotoxicoses HSDN C0231712 Gait waddling C0342282 Symphalangism-brachydactyly syndrome MalaCards|HPO|UMLS C4084766 Vomiting C0206172 Diabetic foot HSDN C0751837 Gait ataxic C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards|HPO C0011991 Loose stools C0035637 Rinderpest HSDN C0018681 Headache, cephalalgia C0001122 Acidosis HSDN C0034933 Abnormal reflexes C0014070 Encephalomyelitis HSDN C1963087 Constipation adverse event C0006118 Brain neoplasms HSDN C0497406 Over weight C0149514 Bronchitis acute HSDN C3539890 Pelvic pain causes awakening at night C0005690 Bladder fistula HSDN C2107731 Consistent cold intolerance C0027145 Myxedema MalaCards C0009806 Constipate C0344434 Atrial fibrillation ecg HSDN C0033377 Caudal displacement C0015938 Fetal macrosomia MalaCards C0747251 Paraparesis spastic progressive C0334082 Nevus, epidermal (disorder) OrphaNet C4085317 Diarrhea frequency C0023420 Mouse leukemia l1210 HSDN C1963065 Apnea adverse event C2984291 Glioblastoma multiforme pathway HSDN C0007758 Cerebellar ataxia C0265201 De sanctis-cacchione syndrome MalaCards|HPO C4084773 Bothered by weight gain C0004030 Aspergillosis HSDN C3665492 Pigmentations C0339539 Familial exudative vitreoretinopathy MalaCards C0150055 Pain chronic C0016658 Fracture bone HSDN C0231218 Malaise generalized C1336312 Stage ii mesothelioma of pleura UMLS C0009676 Confusion state C0678274 Alcohol abstinence HSDN C0000737 Abdomen pain C0878681 Dent's disease OrphaNet C0038002 Spleen enlargement C0796013 Zimmerman laband syndrome MalaCards|HPO C0027497 Queasy C0036875 Disorders of sex development HSDN C4084727 Cough frequency C0022116 Ischemia HSDN C0035232 Diaphragmatic paralysis C0034088 Pulmonary valve insufficiency HSDN C4049644 Depression C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0033774 Skin pruritus C0406355 Acrokeratosis paraneoplastica of bazex MalaCards C0004134 Dyssynergia C0037930 Spinal cord neoplasms HSDN C0751495 Seizure focal C0746265 Lung rml pneumonia UMLS C2024893 Cardiovascular surgery result: fatigue C3665493 Snake bites HSDN C0011991 Loose stools C0035220 Respiratory distress syndrome, newborn HSDN C2024893 Cardiovascular surgery result: fatigue C0032749 Post-kala-azar dermal leishmaniasis MalaCards C0009806 Constipate C0034065 Pulmonary embolism HSDN C0221752 Rbc urine C0272258 Cryoglobulinemia, primary MalaCards C2315100 Pediatric failure to thrive C2931187 Nephropathic cystinosis MalaCards C1963093 Dizziness adverse event C0029401 Osteitis deformans HSDN C0557874 Global developmental delay C1412747 Bbs2 gene HPO C0018772 Deafness C1836824 Amish infantile epilepsy syndrome HPO C0152020 Atony stomach C0268353 Cutis laxa, x-linked MalaCards C4085317 Diarrhea frequency C0600260 Lung diseases, obstructive HSDN C0151908 Dry skin C1866983 Scleroderma, familial progressive MalaCards C0020672 Body temperature decreased C1963137 Hydrocephalus adverse event HSDN C0262384 Chest pain atypical C0741611 Bowel ischemic UMLS C0000737 Abdomen pain C1384687 Ancylostomiasis due to ancylostoma duodenale MalaCards C2984058 Have pain C0009946 Conversion disorder HSDN C1069915 Vertigo C0036357 Psychology, schizophrenic HSDN C0413252 Hypothermia due to exposure C0038454 Cerebrovascular accident HSDN C2936821 Spinal cerebrospinal fluid leak C0035455 Rhinitis HSDN C0022346 Yellow skin C0497327 Dementia HSDN C0917816 Deficiency mental C0238288 Muscular dystrophy, facioscapulohumeral MalaCards|HPO C4084776 Weight loss C0919691 Anastomotic leaks HSDN C0007814 Cerebrospinal fluid otorrhea C0025284 Meningeal neoplasms HSDN C1963091 Diarrhea adverse event C0008325 Cholecystitis HSDN C0020615 Hypoglycemia nos C0574108 Glycerol kinase deficiency - isolated MalaCards C1963091 Diarrhea adverse event C0585442 Osteosarcoma of bone HSDN C0030554 Abnormal sensation C0038531 Subclavian artery stenosis HSDN C2237041 Shox gene with short stature C1956093 Paris-trousseau thrombocytopenia MalaCards C2029884 Hearing loss by exam C0017152 Gastritis HSDN C0009806 Constipate C1846058 Lubs x-linked mental retardation syndrome HPO|UMLS C0851578 Disorder sleep C0017601 Glaucomas HSDN C2029884 Hearing loss by exam C2239176 Liver carcinoma HSDN C0030193 Sense of pain C0152099 Postcholecystectomy syndrome UMLS C0015469 Facial paralysis C0002994 Angioedema HSDN C0042571 Vertigo subjective C0037188 Sinoatrial block HSDN C0040264 Ear ringing sound C0002871 Anemia HSDN C0012833 Dizzy C0266607 Incomplete development of membranous labyrinth UMLS C3829611 Nausea frequency C0011616 Contact dermatitis HSDN C0857305 Thrombocytopenia purpura C0010674 Cystic fibrosis HSDN C0239181 Diarrhea intermittent C0872218 Mitochondrial neurogastrointestinal encephalopathy syndrome MalaCards|HPO|UMLS C0038506 Stutter C0005523 Biological psychiatry HSDN C0042963 Symptoms vomiting C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C4084725 Usual severity cough C1299919 Enteric coccidiosis HSDN C1549543 Administration method - pain C0002991 Cutaneous fibrous histiocytoma HSDN C0349588 Stature short C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C2029884 Hearing loss by exam C0038454 Cerebrovascular accident HSDN C3873641 Pain due to varicose veins of leg C4047600 Pain co-occurrent and due to varicose veins of right leg UMLS C0015672 Decreased energy C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C2700617 Irritation - emotion C0265499 49,xxxxy chromosomal anomaly MalaCards C3163620 Hypotension adverse event C0011311 Dengue fever MalaCards C0015672 Decreased energy C0027746 Nerve degeneration HSDN C4084802 Usual severity diarrhea C0239189 Disaccharide intolerance MalaCards C1962972 Proteinuria adverse event C0220847 C hepatitis virus HSDN C0024031 Back pain lower back C0042826 Field visual HSDN C0010038 Corneal opacity disorder C1835851 Ichthyosis with hypotrichosis, autosomal recessive MalaCards C0032617 High urine output C0022650 Kidney calculi HSDN C0152459 Striae C0206667 Adrenal cortical adenoma MalaCards C0038002 Spleen enlargement C0268490 Tyrosinemia, type i MalaCards|HPO C1384666 Decreased hearing C0024141 Lupus erythematosus, systemic HSDN C1557397 Adverse event associated with pain C1510415 Osteosclerotic myeloma MalaCards C0015672 Decreased energy C0279627 Amml, adult UMLS C0221263 Cafe au lait spot C1836861 Fanconi anemia, complementation group i MalaCards C4085317 Diarrhea frequency C0026691 Mucocutaneous lymph node syndrome OrphaNet|HSDN|MalaCards C0162835 Hypopigmentation C0007965 Chediak-higashi syndrome MalaCards|HPO C4085548 Usual severity dizziness C0033873 Psychiatry HSDN C1963093 Dizziness adverse event C0014544 Epilepsy HSDN C0016199 Pain flank C0278676 Stage ii renal cell cancer UMLS C0151908 Dry skin C1845073 Invasive pneumococcal disease, recurrent isolated, 2 (disorder) MalaCards|HPO C0034124 Pupillary disorder C0020458 Hyperhidrosis disorder HSDN C0022107 Fussiness C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0032797 Postpartum hemorrhage HSDN C0036572 Convulsion C0037188 Sinoatrial block HSDN C0518090 Frequency of pain question C1547046 Kind of quantity - taste HSDN C1963281 Vomiting adverse event C0003873 Rheumatoid arthritis HSDN C0004604 Pain back C0029464 Osteosclerosis HSDN C0002962 Angina C0024305 Lymphoma, non-hodgkin HSDN C0522224 Palsied C0030920 Peptic ulcer HSDN C1963170 Hypothermia adverse event C0848377 Trauma to the abdomen HSDN C1579931 Depressed - symptom C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C0015732 Feces incontinence C0795889 Allan-herndon-dudley syndrome (ahds) OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0149721 Left ventricular hypertrophy HSDN C4085210 Usual severity pain C0525045 Mood disorders HSDN C0518090 Frequency of pain question C0517960 Neurological status: consciousness HSDN C0030193 Sense of pain C0029417 Osteoblastoma HSDN C1963071 Back pain adverse event C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0027497 Queasy C0015328 Behavior, exploratory HSDN C0242936 Center pain C0019285 Diaphragmatic hernia traumatic HSDN C0030552 Paralysis partial C0034929 Reflex HSDN C0018681 Headache, cephalalgia C0002736 Amyotrophic lateral sclerosis HSDN C0005745 Blepharoptosis C2751878 Hadziselimovic syndrome MalaCards C4085210 Usual severity pain C0497572 Female genital herpes HSDN C2919142 Short stature adverse event C2931587 Gemignani syndrome OrphaNet|MalaCards C0018784 Deafness sensorineural C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease OrphaNet|HPO C4085211 Pain distress question C0024667 Animal mammary neoplasms HSDN C4084769 Vomiting frequency C1838979 Mitochondrial complex i deficiency MalaCards|HPO C4084768 Usual severity vomiting C0206671 Eccrine acrospiroma HSDN C0020578 Hyperventilate C0017924 Glycogen storage disease type v HSDN C2024893 Cardiovascular surgery result: fatigue C2973725 Pulmonary arterial hypertension OrphaNet C0034150 Skin purpura C0796561 Melanoma vaccines HSDN C0018772 Deafness C0014547 Epilepsies, partial HSDN C0036572 Convulsion C0034888 Rectal prolapse HSDN C1963184 Nystagmus adverse event C1263846 Attention deficit hyperactivity disorder MalaCards C1279888 Proteinuria of undiagnosed cause C0272295 Purpura, rheumatica MalaCards C4084766 Vomiting C0039841 Thiamine deficiency HSDN C0028738 Nystagmus C1837396 Congenital disorder of glycosylation, type ie MalaCards|HPO C2029884 Hearing loss by exam C0016045 Fibroma HSDN C4084768 Usual severity vomiting C0016483 Food preferences HSDN C0015970 Fever unknown origin C0009240 Cognition HSDN C0020673 Hypothermia (central) (local) C0008626 Congenital chromosomal disease HSDN C1000483 Genus anemia C0003490 Aortic arch syndrome MalaCards C0027796 Neuralgias C0019159 Hepatitis a HSDN C1000483 Genus anemia C0027819 Neuroblastoma MalaCards C0040822 D tremors C4015301 Spinocerebellar ataxia, autosomal recessive 17 MalaCards C2024893 Cardiovascular surgery result: fatigue C0020541 Hypertension, portal HSDN C0042798 Vision dim C1858301 Leber congenital amaurosis 5 MalaCards|HPO C2911647 Weight gain adverse event C0085129 Bronchial hyperreactivity HSDN C0042571 Vertigo subjective C0040136 Thyroid neoplasm HSDN C0013404 Respiratory difficulty C0022658 Kidney diseases HSDN C3641755 Have constipation C0008370 Cholestasis HSDN C0233514 Behavior abnormal C3888138 Monosomy x MalaCards C0917816 Deficiency mental C3150675 Chromosome 15q24 duplication syndrome HPO C0566948 Swelling of vagina C0566943 Vaginal lesion UMLS C0042755 Virilisation C0004903 Beckwith-wiedemann syndrome HSDN C0036572 Convulsion C0282527 Infantile refsum disease (disorder) MalaCards|HPO C4020887 Photodysphoria C1848410 Xeroderma pigmentosum, variant type OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0035358 Retroperitoneal neoplasm HSDN C0042024 Urine incontinence C0001418 Adenocarcinoma HSDN C4085661 Usual severity nausea C0040381 Syndrome tolosa-hunt HSDN C4084802 Usual severity diarrhea C0037421 Social isolation HSDN C1557397 Adverse event associated with pain C0035066 Renal artery obstruction HSDN C0020615 Hypoglycemia nos C0854795 Resectable hepatic malignant neoplasm MalaCards C4085548 Usual severity dizziness C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0026838 Spasticity muscle C0305062 Tetanus toxoids HSDN C0007859 Pain neck C0015397 Disorder of eye HSDN C0032617 High urine output C0019693 Hiv infections HSDN C2984058 Have pain C0026782 Mumps vaccine HSDN C0033774 Skin pruritus C0040053 Thrombosis HSDN C0018772 Deafness C0027665 Neoplasms, nerve tissue HSDN C0577564 Mass of lymphoreticular structure C0686547 Burkitt tumor of lymph nodes of multiple sites UMLS C1557397 Adverse event associated with pain C1963084 Colitis adverse event HSDN C0000737 Abdomen pain C0334123 Histiocytosis, lipoid MalaCards C0750426 Wbc elevated C4080064 Autosomal dominant hereditary pancreatitis MalaCards C0004134 Dyssynergia C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0041105 Jaw spasm C0241158 Cicatrix skin HSDN C0030193 Sense of pain C0032290 Aspiration pneumonia HSDN C0020580 Decreased sensation C0020732 Iatrogenic disease HSDN C0398650 Idiopathic thrombocytopenia purpura C0005967 Bone neoplasms HSDN C0424755 Fever symptoms C2025995 Cellulitis HSDN C0002962 Angina C0010823 Cytomegalovirus infections HSDN C4084776 Weight loss C0022822 Hunchback formed after birth HSDN C0038990 Sweats C3714644 Thymus neoplasms MalaCards C0018681 Headache, cephalalgia C0006818 Campylobacter infection HSDN C0424755 Fever symptoms C0037051 Behavior illness HSDN C0042571 Vertigo subjective C0017409 Herpes zoster oticus DiseaseOntology|MalaCards C0000727 Abdomen acute C0021368 Inflammation HSDN C0019825 Voice hoarseness C0024421 Macroglossia HSDN C0026821 Cramp C0037274 Dermatologic disorders HSDN C4084723 Constipation C2711227 Steatohepatitis HSDN C4020887 Photodysphoria C3281046 Retinitis pigmentosa 64 MalaCards C0700590 Diaphoresis excessive C0343064 Keratolysis exfoliativa OrphaNet|MalaCards C1549543 Administration method - pain C0015625 Fanconi anemia HSDN C0043094 Weight gain C0006145 Breast diseases HSDN C3463815 Feel fatigue C0812393 Cancer patients and suicide and depression HSDN C0034933 Abnormal reflexes C0262593 Injury nerve peripheral HSDN C1961131 Cough adverse event C0002989 Epithelioid hemangioma of skin HSDN C0013404 Respiratory difficulty C0021799 Interprofessional relations HSDN C4085211 Pain distress question C0012813 Diverticulitis HSDN C0013405 Dyspnea, paroxysmal C0027651 Tumor HSDN C0011991 Loose stools C0020502 Hyperparathyroidism HSDN C0020450 Hyperemesis gravidarum C0156692 Mild hyperemesis gravidarum, unspecified as to episode of care or not applicable UMLS C0036572 Convulsion C4015710 Tenorio syndrome MalaCards|UMLS C0037316 Not enough sleeping C0038356 Stomach neoplasms HSDN C0008031 Pain chest C0001122 Acidosis HSDN C4084774 Have weight loss C0013806 Electroplexy shock therapy HSDN C1963184 Nystagmus adverse event C0795902 Coloboma, cleft lip-palate and mental retardation syndrome MalaCards|HPO C3641756 Have diarrhea C0003175 Anthrax disease HSDN C0033377 Caudal displacement C0265451 Chromosome 13q deletion syndrome MalaCards C0009398 Color vision defects C0949628 Uniparental disomy HSDN C0700078 Deep tendon reflex decrease C0023522 Leukodystrophy, metachromatic MalaCards|HPO C0206146 Myocardial stunning C0004239 Atrial flutter HSDN C0858253 Erection inability maintain C0242350 Erectile dysfunction UMLS C0020538 Hbp C1832588 Chromosome 11p11.2 deletion syndrome MalaCards|HPO C0008031 Pain chest C0034929 Reflex HSDN C0151786 Weakness muscle C0013289 Duodenal diseases HSDN C0242936 Center pain C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C0013604 Edematous C0006261 Bronchial diseases HSDN C3274924 Have been coughing C0152937 Primary pneumonic plague DiseaseOntology|MalaCards C0015672 Decreased energy C3178770 Nutcracker syndrome, renal HSDN C0518090 Frequency of pain question C2984302 Leishmaniasis infection pathway HSDN C4084776 Weight loss C0040456 Tooth impaction HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0028242 Nocardia infections HSDN C0019825 Voice hoarseness C1547940 Specimen source codes - ulcer HSDN C0018784 Deafness sensorineural C1838280 Epiphyseal dysplasia, multiple, 1 MalaCards C0030193 Sense of pain C0020555 Hypertrichosis HSDN C2108113 Continuous electrocardiogram ventricular tachycardia C3150690 Left ventricular noncompaction 5 MalaCards C1963170 Hypothermia adverse event C0015695 Fatty liver HSDN C4084784 Diarrhea C0031090 Periodontal diseases HSDN C3665347 Vision impaired C2931837 Hypertryptophanemia MalaCards C0042963 Symptoms vomiting C0409959 Osteoarthritis, knee HSDN C4085210 Usual severity pain C0019195 Hepatitis, viral, human HSDN C4085549 Dizziness C1306759 Eosinophilic disorder HSDN C0031911 Pigment deposition C0346773 Malignant melanoma of ear MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0019034 Hemoglobin sc disease MalaCards|HSDN C2984058 Have pain C0002886 Anemia, macrocytic HSDN C0031911 Pigment deposition C0751291 Desmoplastic medulloblastoma MalaCards C0018926 Emesis bloody C0554309 Prerenal uremia syndrome HSDN C0004093 Asthenia C3163620 Hypotension adverse event HSDN C4084724 Usual severity constipation C0085278 Antiphospholipid syndrome HSDN C3641756 Have diarrhea C0042514 Tachycardia, ventricular HSDN C3641756 Have diarrhea C0026946 Mycoses HSDN C0557874 Global developmental delay C0040560 Toxoplasmosis, congenital MalaCards C1963091 Diarrhea adverse event C0007120 Bronchioloalveolar adenocarcinoma HSDN C4085210 Usual severity pain C0079173 Craniomandibular disorders HSDN C0349588 Stature short C0376524 Branchio-oculo-facial syndrome OrphaNet|HPO|MalaCards C0232466 Feeding difficulty C4040739 3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome MalaCards C3829611 Nausea frequency C0085096 Peripheral vascular diseases HSDN C0033774 Skin pruritus C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C2984057 Have nausea C0026771 Trauma multiple HSDN C2203646 Jaundice C0019163 Hepatitis b DiseaseOntology|MalaCards C0030486 Extremity paralysis, lower C0032587 Polyradiculoneuropathy HSDN C0518090 Frequency of pain question C0233629 Thinking and speaking disturbances HSDN C0042024 Urine incontinence C0033289 Family relationship, professional HSDN C4085210 Usual severity pain C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C1961131 Cough adverse event C0004352 Autistic disorder HSDN C2919142 Short stature adverse event C1851878 Orofacial cleft 8 MalaCards|HPO C0042024 Urine incontinence C0162565 Acute intermittent porphyria MalaCards|HPO C3274924 Have been coughing C0014175 Endometriosis HSDN C1963063 Anorexia adverse event C0003490 Aortic arch syndrome MalaCards C4085211 Pain distress question C0020162 Humerus fracture HSDN C1963180 Neck pain adverse event C0008487 Chordoma HSDN C0009763 Conjunctiva inflammation C0700644 Primary extrapulmonary coccidioidomycosis MalaCards C1549543 Administration method - pain C0008372 Intrahepatic cholestasis HSDN C0557874 Global developmental delay C0796024 Macdermot winter syndrome OrphaNet|MalaCards C4050613 Anxiety C0020428 Hyperaldosteronism MalaCards C0518090 Frequency of pain question C0024205 Lymphadenitis HSDN C1963091 Diarrhea adverse event C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0494475 Seizure generalized tonic clonic C3279875 Cortical malformations, occipital MalaCards C0013395 Indigestion C0027051 Myocardial infarction HSDN C4085862 Bothered by nausea C0524620 Metabolic syndrome x HSDN C0020505 Excessive eating C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C0033774 Skin pruritus C0014121 Bacterial endocarditis HSDN C1557397 Adverse event associated with pain C0024143 Lupus nephritis HSDN C4049602 Hyperactivity C3683846 Chromosome 17p deletion syndrome MalaCards C2169806 Tic C0018564 Hand deformities HSDN C3541349 Syncope C0020595 Hypoaldosteronism HSDN C4084769 Vomiting frequency C0162565 Acute intermittent porphyria MalaCards|HSDN|HPO C2024878 Cardiovascular surgery result: dyspnea C0005779 Blood coagulation disorders HSDN C0019079 Bloody sputum C0747651 Recurrent aspiration pneumonia UMLS C0009460 Communication impairment C0021819 Psychological interview HSDN C2203646 Jaundice C0018916 Hemangioma HSDN C4084725 Usual severity cough C0022116 Ischemia HSDN C0019209 Large liver C1720862 Congenital generalized lipodystrophy type 1 MalaCards|HPO C4084776 Weight loss C1546847 Entity name part type - family HSDN C4084767 Bothered by vomiting C0016627 Avian influenza DiseaseOntology|MalaCards C0034150 Skin purpura C0023448 Lymphoid leukemia HSDN C3463815 Feel fatigue C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0036572 Convulsion C3553349 Coenzyme q10 deficiency, primary, 6 MalaCards C0033774 Skin pruritus C0376547 Aromatherapy HSDN C0015672 Decreased energy C0278769 Chronic lymphocytic leukaemia stage 3 UMLS C0085631 Abnormal excitement C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C2911647 Weight gain adverse event C0024535 Malaria, falciparum HSDN C0013604 Edematous C0029445 Bone necrosis HSDN C4084767 Bothered by vomiting C0024437 Macular degeneration HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041333 Tuberculosis genitourinary HSDN C0019572 Hairiness C0024121 Lung neoplasms HSDN C1963170 Hypothermia adverse event C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0700078 Deep tendon reflex decrease C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease HPO C0424755 Fever symptoms C0027667 Cancer origin unknown HSDN C0917816 Deficiency mental C0795830 Chromosome 9p deletion syndrome OrphaNet|MalaCards C0018681 Headache, cephalalgia C0027831 Neurofibromatosis 1 OrphaNet|HSDN C2024893 Cardiovascular surgery result: fatigue C0702166 Acne HSDN C0000737 Abdomen pain C0028768 Obsessive-compulsive disorder HSDN C4084767 Bothered by vomiting C0005695 Bladder neoplasm HSDN C0039070 Collapse fleeting C3203102 Idiopathic pulmonary arterial hypertension OrphaNet C1963091 Diarrhea adverse event C0040809 Patient refusal of treatment HSDN C4084723 Constipation C1836929 Emanuel syndrome OrphaNet|MalaCards C0018772 Deafness C1868570 Char syndrome MalaCards|HPO C2984057 Have nausea C0751908 Vestibular neuronitis HSDN C0015970 Fever unknown origin C0027804 Fatigue neurosis HSDN C4084723 Constipation C0002871 Anemia HSDN C1963093 Dizziness adverse event C0026896 Myasthenia gravis HSDN C2315100 Pediatric failure to thrive C0043346 Xeroderma pigmentosum OrphaNet|HPO|MalaCards C4084802 Usual severity diarrhea C0042063 Urogenital abnormalities HSDN C0221232 Welts C0413237 Venom-induced angio-edema-urticaria UMLS C0917816 Deficiency mental C3539506 Spastic paraplegia 55, autosomal recessive MalaCards C0003469 Anxiety disorder C0268322 Chester-type porphyria HPO C4084802 Usual severity diarrhea C0020542 Pulmonary hypertension HSDN C0020673 Hypothermia (central) (local) C0026650 Movement disorders HSDN C4084775 Usual severity weight loss C0085207 Gestational diabetes HSDN C0018772 Deafness C1269683 Major depressive disorder HSDN C3641756 Have diarrhea C0019069 Hemophilia a HSDN C0000737 Abdomen pain C2981637 Stage iva hilar cholangiocarcinoma UMLS C0010038 Corneal opacity disorder C0016395 Focal dermal hypoplasia OrphaNet|HPO|MalaCards C0917816 Deficiency mental C0270724 Infantile neuroaxonal dystrophy HPO C2911647 Weight gain adverse event C0042373 Vascular diseases HSDN C0151889 Reflexes tendon increased C1861457 Progressive encephalomyelitis with rigidity MalaCards C0344365 Incomplete emptying of bladder C0810038 Genitourinary symptoms and ill-defined conditions UMLS C2024893 Cardiovascular surgery result: fatigue C0018801 Heart failure HSDN C0020578 Hyperventilate C0014548 Epilepsy, generalized HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162309 Adrenoleukodystrophy HSDN C0010520 Skin cyanosis C0026769 Multiple sclerosis HSDN C0019825 Voice hoarseness C0206637 Chondrosarcoma, mesenchymal HSDN C4085211 Pain distress question C0024205 Lymphadenitis HSDN C0518090 Frequency of pain question C0022367 Jaw, edentulous, partially HSDN C0151889 Reflexes tendon increased C3807295 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant MalaCards C1557397 Adverse event associated with pain C0008373 Cholesteatoma HSDN C1557397 Adverse event associated with pain C0041971 Tumor urethra HSDN C0020578 Hyperventilate C2931660 Autosomal recessive fructose 1, 6-diphosphatase deficiency MalaCards C0518090 Frequency of pain question C2936490 Cardiac arrest, out-of-hospital HSDN C1963091 Diarrhea adverse event C0033247 Proctocolitis HSDN C0751295 Memory loss or impairment C1858991 Childhood ataxia with central nervous system hypomyelinization MalaCards|HPO|UMLS C0005745 Blepharoptosis C1833102 Diabetes mellitus, permanent neonatal, with neurologic features HPO C0009398 Color vision defects C1548578 Location characteristic id - smoking HSDN C0019214 Hepatosplenomegaly C0040558 Toxoplasmosis DiseaseOntology C0004134 Dyssynergia C1853554 Radiation induced meningioma MalaCards C0018772 Deafness C2028283 History of premature birth HSDN C0023380 Lethargy C0175683 Citrullinemia HPO|UMLS C0014089 Functional encopresis C1968835 Egot gene HSDN C3463815 Feel fatigue C0700208 Acquired scoliosis HSDN C0003113 Anomia C0014547 Epilepsies, partial HSDN C0018772 Deafness C1859309 Syndactyly cenani lenz type MalaCards C2984057 Have nausea C0556520 Psychological desensitization HSDN C0036659 Sensation disorder C0042994 Vulvar diseases HSDN C0015300 Ocular proptosis C1869122 Ehlers-danlos syndrome, progeroid form HPO C0004134 Dyssynergia C3150730 Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency HPO C0000727 Abdomen acute C0024232 Lymphatic metastasis HSDN C0018681 Headache, cephalalgia C0014175 Endometriosis HSDN C0036572 Convulsion C1547940 Specimen source codes - ulcer HSDN C0021177 Libido increased C0855242 Disturbance in sexual arousal UMLS C0020673 Hypothermia (central) (local) C0023176 Lead poisoning HSDN C3829611 Nausea frequency C0009374 Colonic disease, functional HSDN C0727671 Red cross toothache drops C1579931 Depressed - symptom HSDN C0015468 Face pain C0042373 Vascular diseases HSDN C0037763 Spasm C0032019 Pituitary neoplasms HSDN C1557397 Adverse event associated with pain C0041952 Uerterolithiasis HSDN C0019572 Hairiness C0030297 Pancreatic neoplasm HSDN C0020649 Blood pressure decreased C0238027 Botulism, infantile OrphaNet|MalaCards C0016199 Pain flank C0004601 Back injury HSDN C2919142 Short stature adverse event C0265205 Robinow syndrome MalaCards|HPO C3641756 Have diarrhea C0024215 Lymphangiectasis, intestinal OrphaNet|MalaCards C0030552 Paralysis partial C2242765 Acquired spondylolisthesis HSDN C4085211 Pain distress question C3665624 Serum calcium below normal HSDN C2984057 Have nausea C0036974 Shock HSDN C0232466 Feeding difficulty C1970253 Phosphoserine aminotransferase deficiency MalaCards C0013456 Pain ear C0005940 Bone diseases HSDN C0009398 Color vision defects C0017979 Glycosuria HSDN C0015672 Decreased energy C0027666 Neoplasms, radiation-induced HSDN C0547030 Sensory perceptual alteration: visual C1691006 Dysphotopsia UMLS C0040822 D tremors C0041408 Turner syndrome HSDN C1963091 Diarrhea adverse event C0020625 Hyponatremia HSDN C2315100 Pediatric failure to thrive C0162283 Nephrogenic diabetes insipidus OrphaNet|HSDN|HPO C3641755 Have constipation C0795907 Conotruncal anomaly face syndrome OrphaNet|HPO|MalaCards C1963180 Neck pain adverse event C0039984 Thoracic outlet syndrome HSDN C0011991 Loose stools C0040336 Tobacco use disorder HSDN C1963065 Apnea adverse event C1842704 Gaucher disease, perinatal lethal MalaCards|HPO C0036396 Sciatica C0042373 Vascular diseases HSDN C0013595 Eczematous dermatitis C0175691 Dubowitz syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0040761 Transposition of great vessels HSDN C0557874 Global developmental delay C0265241 Franceschetti-klein syndrome MalaCards|HPO C0008031 Pain chest C0264743 Rheumatic fever without heart involvement MalaCards C4085211 Pain distress question C0023676 Life style HSDN C0009676 Confusion state C0162532 Variegate porphyria MalaCards|HPO C0015672 Decreased energy C1299262 Sarcoma - category (morphologic abnormality) HSDN C0036572 Convulsion C0405580 Adrenal cortical hypofunction HSDN C0003862 Pain joint C1854896 Mucolipidosis iii gamma MalaCards|HPO|UMLS C0013362 Dysarthrias C0268407 Senile cardiac amyloidosis MalaCards C0041105 Jaw spasm C0029400 Osteitis HSDN C0013404 Respiratory difficulty C0039978 Thoracic diseases HSDN C4085222 Nausea C0034530 Injury radiation HSDN C0018772 Deafness C3149750 Mitochondrial dna depletion syndrome 2 (myopathic type) MalaCards|HPO C0042963 Symptoms vomiting C0344423 Atrial flutter by ecg finding HSDN C3898969 Have been vomiting C0034929 Reflex HSDN C0020538 Hbp C1868139 Medullary cystic kidney disease 1 MalaCards|HPO C4084784 Diarrhea C0439840 Reflex motion descriptor HSDN C0085636 Light sensitivity C0038325 Stevens-johnson syndrome HSDN|HPO C0917816 Deficiency mental C1849096 Infantile onset spinocerebellar ataxia MalaCards|HPO C1145670 Failure respiratory C0268576 Hyperleucinemia OrphaNet C0026821 Cramp C0023119 Lathyrism HSDN C0030486 Extremity paralysis, lower C0023370 Aortic occlusion distal chronic HSDN C0000727 Abdomen acute C0206630 Endometrial stromal sarcoma HSDN C2911645 Weight loss adverse event C0011615 Dermatitis, atopic HSDN C3898969 Have been vomiting C1855849 Bartter syndrome, antenatal , type 2 HPO C4085210 Usual severity pain C0029124 Optic atrophy HSDN C1963281 Vomiting adverse event C0033953 Psychosexual disorders HSDN C1962972 Proteinuria adverse event C0033817 Pseudomonas infections HSDN C1962972 Proteinuria adverse event C0003469 Anxiety disorders HSDN C4084802 Usual severity diarrhea C0016548 Foreign body migration HSDN C0242936 Center pain C1963164 Lymphopenia adverse event HSDN C0497247 Blood pressure elevation C1970820 Fabry disease, cardiac variant HPO C2029884 Hearing loss by exam C0017658 Glomerulonephritis HSDN C4085661 Usual severity nausea C0003496 Aortic rupture HSDN C1962976 Ventricular fibrillation adverse event C2751898 Ventricular fibrillation, paroxysmal familial, 1 HPO C0015672 Decreased energy C0559260 Congenital scoliosis HSDN C0011991 Loose stools C1857449 Cutaneous photosensitivity and colitis, lethal MalaCards C0009806 Constipate C0041327 Tuberculosis, pulmonary HSDN C2029884 Hearing loss by exam C0236969 Substance-related disorders HSDN C0413252 Hypothermia due to exposure C2940786 Thyroid hormone resistance syndrome HPO C0019214 Hepatosplenomegaly C3665444 Neutrophilia (disorder) MalaCards C0011991 Loose stools C0026691 Mucocutaneous lymph node syndrome OrphaNet|HSDN|MalaCards C0010200 Cough symptom C3887662 Intraspinal neoplasm HSDN C0030552 Paralysis partial C1720189 Episodic ataxia MalaCards C0015468 Face pain C0018790 Cardiac arrest HSDN C0034933 Abnormal reflexes C0001849 Aids dementia complex HSDN C0015672 Decreased energy C1762616 Meningioma, benign, no icd-o subtype HSDN C0040264 Ear ringing sound C0007133 Carcinoma, papillary HSDN C3539022 Pelvic pain decreasing in severity C0010709 Cyst HSDN C4085317 Diarrhea frequency C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C1971624 Appetite absent C0017178 Gastrointestinal diseases HSDN C2203646 Jaundice C0162872 Aortic aneurysm, thoracic HSDN C0003467 Angst C2932715 Pseudohypoparathyroidism type 1b MalaCards|HPO C4084776 Weight loss C1962976 Ventricular fibrillation adverse event HSDN C0007758 Cerebellar ataxia C1849722 Polyglucosan body disease, adult form MalaCards|HPO C1963066 Joint pain adverse event C0021368 Inflammation MalaCards C0026603 Motion sickness C0032787 Postoperative complications HSDN C1959630 Eye pain adverse event C0008522 Choroid, hemorrhage HSDN C2073625 X-ray of chest: pleural effusion C0281479 Primary systemic amyloidosis MalaCards C0020578 Hyperventilate C0453996 Tobacco smoking HSDN C0232466 Feeding difficulty C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards|HPO C4085211 Pain distress question C0524851 Neurodegenerative disorders HSDN C1384666 Decreased hearing C0524910 Hepatitis c, chronic HSDN C0000727 Abdomen acute C0007350 Cat disease HSDN C4084784 Diarrhea C1970712 Multiple endocrine neoplasia, type iv OrphaNet|HPO|MalaCards C0339250 Melanin pigmentation of cornea C0271278 Krukenberg spindle UMLS C0080274 Retention urinary C0042781 Visceral myopathy MalaCards C0015469 Facial paralysis C0010246 Coxsackievirus infections HSDN C0460137 Push down or depress C3811918 Grn-related frontotemporal dementia MalaCards C4084769 Vomiting frequency C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0000737 Abdomen pain C0206724 Sex cord-stromal tumor HSDN C0221232 Welts C1275344 Bullous urticaria pigmentosa UMLS C0013362 Dysarthrias C0023524 Leukoencephalopathy, progressive multifocal DiseaseOntology C1557397 Adverse event associated with pain C0007121 Bronchogenic carcinoma HSDN C0020672 Body temperature decreased C0041022 Pulmonary valve, stenosis, with patent foramen ovale HSDN C0007758 Cerebellar ataxia C2673873 Bardet-biedl syndrome 13 HPO C0015230 Exanthem C0571458 Ceftazidime allergy UMLS C0020672 Body temperature decreased C3489413 Lipomatosis, multiple HSDN C0018524 Hallucinate C0085096 Peripheral vascular diseases HSDN C0000737 Abdomen pain C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0015672 Decreased energy C0085278 Antiphospholipid syndrome HSDN C3887784 Decreased urine output C0026766 Multiple organ failure HSDN C1963086 Confusion adverse event C0006109 Brain damage, chronic HSDN C0518090 Frequency of pain question C0035793 Rocky mountain spotted fever HSDN C4085211 Pain distress question C0040156 Thyrotoxicosis HSDN C4084767 Bothered by vomiting C0033873 Psychiatry HSDN C0030193 Sense of pain C0033847 Pseudoxanthoma elasticum HSDN C0020455 Hypergammaglobulinemia C0019624 Histiocytosis, non-langerhans-cell HSDN C4085211 Pain distress question C1704212 Embolism embolus HSDN C4084724 Usual severity constipation C0036439 Scoliosis, unspecified HSDN C0018681 Headache, cephalalgia C0036916 Sexually transmitted diseases HSDN C0020673 Hypothermia (central) (local) C2586211 Thrombosis of blood vessel HSDN C0033774 Skin pruritus C0272203 Indolent systemic mastocytosis OrphaNet|MalaCards C3641755 Have constipation C0025202 Melanoma HSDN C3829611 Nausea frequency C1854107 Hyperaldosteronism, familial, type ii MalaCards C0242936 Center pain C1610547 Production class code - pleasure HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206062 Lung diseases, interstitial HSDN C0004134 Dyssynergia C2239176 Liver carcinoma HSDN C4085222 Nausea C0038579 Substance abuse, intravenous HSDN C0242936 Center pain C0014009 Empyema HSDN C2315100 Pediatric failure to thrive C0030286 Pancreatic diseases MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0017662 Glomerulonephritis, membranoproliferative HSDN C0522224 Palsied C0004275 Attitude health HSDN C0009460 Communication impairment C0600104 Obsessive compulsive behavior HSDN C4084774 Have weight loss C0238067 Colitis, collagenous HSDN C4084724 Usual severity constipation C0008325 Cholecystitis HSDN C0424755 Fever symptoms C1415614 Hmgcl gene HPO C0424755 Fever symptoms C0031762 Photosensitivity disorders HSDN C0040034 Thrombocytopenia C0015773 Felty syndrome MalaCards C0037316 Not enough sleeping C0034088 Pulmonary valve insufficiency HSDN C2203646 Jaundice C0023473 Myeloid leukemia, chronic HSDN C0030193 Sense of pain C0013504 Echinococcosis, hepatic HSDN C1962972 Proteinuria adverse event C0340629 Aortic aneurysm without mention of rupture nos HSDN C3898969 Have been vomiting C0027809 Neurilemmoma HSDN C4085210 Usual severity pain C0038579 Substance abuse, intravenous HSDN C0042798 Vision dim C2676042 Skin-hair-eye pigmentation, variation in, 4 HPO C0018681 Headache, cephalalgia C3647010 Periodic headache syndromes UMLS C4084775 Usual severity weight loss C0334419 Pheochromocytoma, malignant MalaCards C0015300 Ocular proptosis C1863959 Hyperthyroidism, familial gestational MalaCards|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011616 Contact dermatitis HSDN C2911645 Weight loss adverse event C0038362 Stomatitis HSDN C2037135 Sudden loss of vision in temporal half of visual field C0018979 Hemianopsia UMLS C0234376 Tremor action C1861732 Spinocerebellar ataxia 29 UMLS C0522224 Palsied C0031511 Pheochromocytoma HSDN C0008031 Pain chest C0238015 Autonomic dysreflexia UMLS C3665386 Abnormal vision C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C1963184 Nystagmus adverse event C1956390 Cranial arteritis MalaCards C0700590 Diaphoresis excessive C0795878 Monosomy 22 MalaCards C0040264 Ear ringing sound C3888123 Deafness, autosomal dominant 50 MalaCards C0002962 Angina C0021833 Intestinal fistula HSDN C2984058 Have pain C1962974 Chylothorax adverse event HSDN C2315100 Pediatric failure to thrive C0235146 Emotionally high HSDN C1565249 Limitation, mobility C0027765 Nervous system disorder HSDN C4085222 Nausea C0020255 Hydrocephalus HSDN C0242936 Center pain C0242231 Coronary stenosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3714514 Infection HSDN C3665492 Pigmentations C0014145 Yolk sac tumor MalaCards C4084802 Usual severity diarrhea C0018939 Hematological disease HSDN C0184567 Pain acute C0376547 Aromatherapy HSDN C3665347 Vision impaired C1857572 Corneal dystrophy and perceptive deafness OrphaNet|HPO C0040822 D tremors C3827868 Tachycardia by ecg finding HSDN C0019825 Voice hoarseness C1853723 Myopathy, distal 2 MalaCards|HPO C2919142 Short stature adverse event C0155338 Total ophthalmoplegia MalaCards C0013404 Respiratory difficulty C0021833 Intestinal fistula HSDN C4084725 Usual severity cough C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0009806 Constipate C2103078 Colonic and rectal disorders UMLS C2919142 Short stature adverse event C0431406 Asymmetric crying face association OrphaNet|HPO|MalaCards C0023015 Language handicap C0033975 Psychotic disorders HSDN C0270948 Neurogenic muscular atrophy C3502298 Lactic acidosis, fatal infantile MalaCards C1971624 Appetite absent C0272295 Purpura, rheumatica MalaCards C0037316 Not enough sleeping C0038587 Substance withdrawal syndrome HSDN C0575081 Abnormal gait C3279839 Mental retardation, autosomal dominant 7 MalaCards C1549543 Administration method - pain C0241961 Angiomyolipoma of kidney HSDN C0349588 Stature short C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C1961131 Cough adverse event C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0030193 Sense of pain C1527348 Brain hypoxia HSDN C3665347 Vision impaired C1843815 Newfoundland rod-cone dystrophy MalaCards|HPO C0030486 Extremity paralysis, lower C0006434 Burn injury HSDN C4085210 Usual severity pain C0282504 Environmental allergies HSDN C2237041 Shox gene with short stature C0027341 Nail-patella syndrome MalaCards|HPO C4084727 Cough frequency C0702221 Tactual discrimination HSDN C4085642 Level of joint stiffness C2931323 Heart-hand syndrome 2 OrphaNet|MalaCards C4082202 Sleep quality question C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0013604 Edematous C0009062 Clostridia infection HSDN C0033774 Skin pruritus C0033975 Psychotic disorders HSDN C1962972 Proteinuria adverse event C2930923 N-acetylneuraminic acid storage disease MalaCards C1962972 Proteinuria adverse event C0268250 Gaucher disease, type 2 (disorder) MalaCards C0040485 Wryneck C0020458 Hyperhidrosis disorder HSDN C0018772 Deafness C0406704 Rudiger syndrome 1 MalaCards C4084802 Usual severity diarrhea C0035091 Renal tubular transport, inborn errors HSDN C0011991 Loose stools C0026850 Muscular dystrophy HSDN C2362324 Pediatric obesity C0015618 Families therapy HSDN C2096293 Ent surgical result ear vertigo C0524812 Intracranial hypotension HSDN C4084768 Usual severity vomiting C0268293 Corticosterone methyl oxidase type i deficiency HPO C2073625 X-ray of chest: pleural effusion C0343206 Hypocomplementemic urticarial vasculitis MalaCards C0851578 Disorder sleep C0018235 Aggrieved HSDN C2911647 Weight gain adverse event C0020507 Hyperplasia HSDN C0030193 Sense of pain C0039483 Giant cell arteritis HSDN C0038506 Stutter C3888013 Hypnoses HSDN C4085211 Pain distress question C0010967 Behavior, dangerous HSDN C0041657 Consciousness loss C1968835 Egot gene HSDN C0162834 Hyperpigmentation C2673610 Jeb-i MalaCards C1963170 Hypothermia adverse event C0025521 Inborn errors of metabolism HSDN C1510417 Apraxia of gait C0006105 Brain abscess HSDN C3887873 Hearing loss C0010266 Cranial nerve diseases HSDN C0018524 Hallucinate C0023448 Lymphoid leukemia HSDN C0009421 Comatose C1855255 Pseudoarylsulfatase a deficiency MalaCards C2984058 Have pain C0017128 Fistula gastric HSDN C0037316 Not enough sleeping C0236969 Substance-related disorders HSDN C4085222 Nausea C0013514 Echinostomiasis DiseaseOntology C0002965 Crescendo angina C0009375 Colonic neoplasms HSDN C1963067 Atrial fibrillation adverse event C2678478 Brugada syndrome 3 MalaCards|HPO C1263846 Attention deficit disorder with hyperactivity C2678416 Hyperphenylalaninemia, non-pku mild HPO C1557397 Adverse event associated with pain C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0860603 Anxiety symptom C0751157 Fraxe syndrome MalaCards C4085222 Nausea C2239176 Liver carcinoma HSDN C0233514 Behavior abnormal C0034494 Rabies (disorder) OrphaNet|MalaCards C0018834 Brash C1846058 Lubs x-linked mental retardation syndrome HPO C1962972 Proteinuria adverse event C0018790 Cardiac arrest HSDN C0039070 Collapse fleeting C0007097 Carcinomas HSDN C1963065 Apnea adverse event C0686721 Babies shaken HSDN C0015468 Face pain C0010261 Crack tooth HSDN C0151786 Weakness muscle C0014474 Ependymoma HSDN C0002962 Angina C3714639 Exit block by ecg finding HSDN C1557397 Adverse event associated with pain C0376549 Roseolovirus infections HSDN C0221263 Cafe au lait spot C0022603 Seborrheic keratosis HSDN C0030552 Paralysis partial C0011615 Dermatitis, atopic HSDN C0004604 Pain back C1300028 Disorder characterised by pain UMLS C3641755 Have constipation C0017075 Ganglioneuroma HSDN C0497247 Blood pressure elevation C1859570 Bardet-biedl syndrome 12 HPO C4085210 Usual severity pain C0017924 Glycogen storage disease type v HSDN C0085636 Light sensitivity C0009759 Conjunctival diseases HSDN C1384666 Decreased hearing C1832438 Chitty hall baraitser syndrome OrphaNet|MalaCards C0030552 Paralysis partial C0036974 Shock HSDN C0042798 Vision dim C0015310 Exotropia HSDN C0009421 Comatose C3146297 Study of behavior during childhood HSDN C0013144 Drowsy C0268630 Hyper-beta-alaninemia MalaCards C1557397 Adverse event associated with pain C0013298 Duodenitis HSDN C4085210 Usual severity pain C0751792 Trauma, nervous system HSDN C4084723 Constipation C0702166 Acne HSDN C2911645 Weight loss adverse event C0001122 Acidosis HSDN C1963065 Apnea adverse event C0022116 Ischemia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0039590 Testicular neoplasms HSDN C1963091 Diarrhea adverse event C0162557 Liver failure, acute HSDN C0027796 Neuralgias C0037744 Perceptual spatial orientation HSDN C0152169 Colic renal C0042075 Urologic diseases UMLS C0026821 Cramp C0276786 Human balantidiasis MalaCards C0155344 Spasm of conjugated gaze C0702143 Conjugate; gaze, palsy UMLS C0026821 Cramp C0042131 Uterine diseases HSDN C4084802 Usual severity diarrhea C0032326 Pneumothorax HSDN C0018784 Deafness sensorineural C0271829 Pendred's syndrome OrphaNet|HPO|MalaCards C1963065 Apnea adverse event C0040580 Tracheal diseases HSDN C0018777 Deafness, conductive C0031900 Pierre robin syndrome HSDN C0221166 Paraparesis C0020255 Hydrocephalus HSDN C0005745 Blepharoptosis C1266101 Thymic epithelial tumor OrphaNet C0424755 Fever symptoms C0006147 Breast fed HSDN C0010200 Cough symptom C0520757 Delayed emergence from anesthesia HSDN C0426579 Anorexia symptom C0021655 Insulin resistance HSDN C0003113 Anomia C0702221 Tactual discrimination HSDN C0242936 Center pain C0376618 Endotoxemia HSDN C4084775 Usual severity weight loss C0162872 Aortic aneurysm, thoracic HSDN C2911647 Weight gain adverse event C0520946 Emotional hypersensitivity HSDN C0030975 Disorders perception C0009946 Conversion disorder HSDN C0242936 Center pain C0009186 Coccidioidomycosis HSDN C4084788 Have dizziness C0041755 Adverse reaction to drug HSDN C4084727 Cough frequency C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C4084788 Have dizziness C0008350 Cholelithiasis HSDN C0015469 Facial paralysis C0043541 Zygomycoses HSDN C2203646 Jaundice C0034065 Pulmonary embolism HSDN C0000727 Abdomen acute C0036983 Septic shock HSDN C0019214 Hepatosplenomegaly C0035022 Tick-borne relapsing fever DiseaseOntology|MalaCards C0086437 Joint hypermobility C4015558 Temple syndrome MalaCards C4085210 Usual severity pain C0003615 Appendicitis MalaCards C0003811 Cardiac rhythm disturbance C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards C0018772 Deafness C0027441 Nasopharyngitis HSDN C1963071 Back pain adverse event C2711227 Steatohepatitis HSDN C0151686 Growth retardation C0206667 Adrenal cortical adenoma MalaCards C4084769 Vomiting frequency C0002991 Cutaneous fibrous histiocytoma HSDN C0018777 Deafness, conductive C1834818 Mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones HPO C1557397 Adverse event associated with pain C0038325 Stevens-johnson syndrome HSDN C0042963 Symptoms vomiting C0016171 Fistula of intestine, excluding rectum and anus HSDN C1557397 Adverse event associated with pain C0014901 Aesthetic HSDN C0042963 Symptoms vomiting C1707400 Classic medulloblastoma UMLS C2984057 Have nausea C0009240 Cognition HSDN C2024878 Cardiovascular surgery result: dyspnea C0026769 Multiple sclerosis HSDN C3641756 Have diarrhea C2347126 Microscopic polyarteritis MalaCards C4084784 Diarrhea C0020523 Immediate hypersensitivity HSDN C0013395 Indigestion C0041296 Tuberculosis HSDN C0518090 Frequency of pain question C0038940 Surgical wound dehiscence HSDN C4085317 Diarrhea frequency C0020473 Hyperlipidemia HSDN C0042963 Symptoms vomiting C0024121 Lung neoplasms HSDN C3641756 Have diarrhea C0033626 Protein deficiency HSDN C4084774 Have weight loss C0007282 Carotid stenosis HSDN C0312416 Morning sickness C0012242 Digestive system disorders HSDN C0085593 Chill C0034929 Reflex HSDN C0030193 Sense of pain C0242647 Mucosa-associated lymphoid tissue lymphoma HSDN C0031315 Phantom limb pain C0027051 Myocardial infarction HSDN C0020458 Hyperhydrosis C0019829 Hodgkin disease OrphaNet C0019825 Voice hoarseness C0022423 Judgement HSDN C3665346 Loss sight C1837073 Spondylometaphyseal dysplasia with cone-rod dystrophy OrphaNet|HPO C3463815 Feel fatigue C3714514 Infection HSDN C0018772 Deafness C2931760 Acrocallosal syndrome, schinzel type MalaCards|HPO C4085211 Pain distress question C0013533 Echovirus infections HSDN C0018777 Deafness, conductive C0001080 Achondroplasia OrphaNet|HSDN|HPO|MalaCards C1962972 Proteinuria adverse event C0342488 Mineralocorticoid excess syndrome, apparent HSDN C0039070 Collapse fleeting C0003873 Rheumatoid arthritis HSDN C0009806 Constipate C2981399 Stage iib colorectal cancer UMLS C3665347 Vision impaired C0345407 Osteopetrosis, autosomal recessive 3 HPO C0518090 Frequency of pain question C1636667 Disorder characterized by eosinophilia HSDN C1963246 Sinus tachycardia adverse event C0221056 Adult type dermatomyositis MalaCards C0026826 High muscle tone C0018609 Hartnup disease MalaCards|HPO C4085210 Usual severity pain C0002895 Anemia, sickle cell OrphaNet|MalaCards C1963071 Back pain adverse event C0033289 Family relationship, professional HSDN C1963180 Neck pain adverse event C0014836 Escherichia coli infections HSDN C1963175 Sinus bradycardia adverse event C1837845 Sick sinus syndrome 1, autosomal recessive MalaCards|HPO C0030193 Sense of pain C0020532 Hypersplenism HSDN C3887638 Failure to thrive in infant C0019621 Histiocytosis, langerhans-cell HSDN C1962972 Proteinuria adverse event C0036916 Sexually transmitted diseases HSDN C4085210 Usual severity pain C0018235 Aggrieved HSDN C4085317 Diarrhea frequency C0026850 Muscular dystrophy HSDN C0221423 Ailment C0679247 Disease end stage UMLS C0233794 Memory impaired C0017636 Glioblastoma MalaCards C0020580 Decreased sensation C0034735 Raynaud phenomenon HSDN C2984058 Have pain C1510412 Pseudoaneurysm HSDN C0018681 Headache, cephalalgia C0020651 Hypotension, orthostatic HSDN C0018772 Deafness C1844862 Abruzzo erickson syndrome MalaCards|HPO C1962972 Proteinuria adverse event C0700095 Central neuroblastoma HSDN C0522224 Palsied C0023290 Leishmaniasis, visceral HSDN C4085548 Usual severity dizziness C0018800 Cardiomegaly HSDN C0700078 Deep tendon reflex decrease C3150667 Microcephaly, seizures, and developmental delay MalaCards|HPO C0033377 Caudal displacement C0432442 Chromosome 18p deletion syndrome OrphaNet|MalaCards C0028738 Nystagmus C2751308 Cone dystrophy 4 (disorder) MalaCards|HPO C0013428 Painful urination C0268120 Adenine phosphoribosyltransferase deficiency MalaCards|HPO C4049644 Depression C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0008031 Pain chest C0477611 Spin osteochondrosis, unsp HSDN C1962956 Flatulence adverse event C0002438 Amebiasis HSDN C4085862 Bothered by nausea C0302497 Retrobulbar haemorrhage HSDN C0040485 Wryneck C1847640 Kufor-rakeb syndrome MalaCards|HPO|UMLS C4084768 Usual severity vomiting C0040997 Trigeminal neuralgia HSDN C1557397 Adverse event associated with pain C0037774 Spatial behavior HSDN C0038002 Spleen enlargement C0393591 Aicardi-goutieres syndrome HPO C1279888 Proteinuria of undiagnosed cause C2711227 Steatohepatitis HSDN C0030193 Sense of pain C0015556 Fallopian tube diseases HSDN C0015672 Decreased energy C0001403 Addison disease OrphaNet C0021359 Infertility C1839841 Spermatogenic failure, x-linked, 2 MalaCards C1963249 Tinnitus adverse event C0001973 Alcoholic intoxication, chronic HSDN C0030200 Intractable pain C0037930 Spinal cord neoplasms HSDN C0000731 Abdomen distention C2931002 Congenital disorder of glycosylation type 1h MalaCards C0242936 Center pain C0206721 Inverted papilloma HSDN C0035078 Failure kidney C1857389 Cystinuria, type b MalaCards|HPO C2919142 Short stature adverse event C1956093 Paris-trousseau thrombocytopenia MalaCards C0349588 Stature short C1849437 Mainzer-saldino disease MalaCards|HPO C0018681 Headache, cephalalgia C0343068 Familial cold urticaria OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0013418 Abnormal labor HSDN C3539896 Pelvic pain occurs with urination C0004275 Attitude health HSDN C0003862 Pain joint C0002940 Aneurysm HSDN C4085210 Usual severity pain C1527336 Sjogren's syndrome HSDN C0013404 Respiratory difficulty C3814778 Hemolytic index HSDN C0005745 Blepharoptosis C0085920 Brachial neuralgia MalaCards C0018784 Deafness sensorineural C3808414 Perrault syndrome 3 MalaCards C1069915 Vertigo C0853697 Neutrophil count decreased HSDN C4085210 Usual severity pain C0272375 Antithrombin iii deficiency HSDN C4085210 Usual severity pain C0026654 Moyamoya disease HSDN C0151825 Ostalgia C0345904 Malignant neoplasm of liver MalaCards C2242996 Tingling C1963067 Atrial fibrillation adverse event HSDN C0232466 Feeding difficulty C3553358 Coenzyme q10 deficiency, primary, 3 MalaCards C0002962 Angina C0040435 Tooth diseases HSDN C1963091 Diarrhea adverse event C3276706 Small fiber neuropathy MalaCards C4084768 Usual severity vomiting C0206083 Myelinoclasis, central pontine HSDN C0018772 Deafness C0030790 Pelvis infection HSDN C0018772 Deafness C1850626 Nathalie syndrome MalaCards C4084802 Usual severity diarrhea C0004352 Autistic disorder HSDN C4085548 Usual severity dizziness C0042133 Uterine fibroids HSDN C0019825 Voice hoarseness C0345946 Epidermoid carcinoma of trachea UMLS C0917816 Deficiency mental C1832431 Digeorge syndrome-velocardiofacial syndrome complex 2 OrphaNet|MalaCards C0025323 Bleeding menstrual heavy C0015503 Factor vii deficiency OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0008149 Chlamydia infections HSDN C0018681 Headache, cephalalgia C1456660 Monkeypox virus infections MalaCards C3665347 Vision impaired C0027859 Acoustic neuroma HPO C1263846 Attention deficit disorder with hyperactivity C3150999 Chromosome 7q11.23 deletion syndrome, distal, 1.2-mb MalaCards C0152029 Sinus congestion C0948349 Respiratory tract congestion UMLS C0036572 Convulsion C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0042928 Paralysis vocal cord C1546847 Entity name part type - family HSDN C0039070 Collapse fleeting C0497327 Dementia HSDN C0008031 Pain chest C0032963 Pregnancy complications, cardiovascular HSDN C0271234 Low vision, both eyes unspec. C0392571 B.eye-mvi, l eye-low vis.unsp. UMLS C0026821 Cramp C0175713 Aicardi's syndrome HSDN C0003811 Cardiac rhythm disturbance C3809288 Left ventricular noncompaction 8 MalaCards C0232466 Feeding difficulty C0268547 Argininosuccinic aciduria MalaCards C4085548 Usual severity dizziness C0393571 Multiple system atrophy HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004364 Autoimmune diseases HSDN C0018784 Deafness sensorineural C0020732 Iatrogenic disease HSDN C1963184 Nystagmus adverse event C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0242936 Center pain C0042143 Uterine rupture HSDN C0024031 Back pain lower back C0004275 Attitude health HSDN C0454539 Covert stammering C0038506 Stuttering UMLS C0018777 Deafness, conductive C0345382 Gorlin chaudhry moss syndrome OrphaNet C0015970 Fever unknown origin C0021051 Immunologic deficiency syndromes HSDN C0040822 D tremors C1709872 Recurrent adrenal gland chromaffin neoplasm UMLS C0150055 Pain chronic C0012979 Canine disease HSDN C0011991 Loose stools C0019054 Hemolysis (disorder) HSDN C0020538 Hbp C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive MalaCards C0010200 Cough symptom C0019337 Heroin dependence HSDN C4085549 Dizziness C0021783 Internal external locus of control HSDN C1557397 Adverse event associated with pain C0242966 Systemic inflammatory response syndrome HSDN C3539889 Pelvic pain increasing in severity C0019310 Hernia, obturator HSDN C3815497 Cough C0039685 Tetralogy of fallot HSDN C0036396 Sciatica C0751931 Femoral lesion nerve HSDN C0033774 Skin pruritus C0017638 Glioma HSDN C3274924 Have been coughing C2239253 Aneurysm of sinus of valsalva MalaCards C0151786 Weakness muscle C0035222 Respiratory distress syndrome, adult HSDN C4084769 Vomiting frequency C0409959 Osteoarthritis, knee HSDN C0026838 Spasticity muscle C4014708 Hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies MalaCards|UMLS C4084776 Weight loss C0023467 Leukemia, myelocytic, acute HSDN C0557874 Global developmental delay C3149276 Chromosome 16p12.1 deletion syndrome, 520-kb HPO C0030975 Disorders perception C0004095 Asthenopia HSDN C1535893 Orthostatic intolerance C0751908 Vestibular neuronitis HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0001418 Adenocarcinoma HSDN C4084768 Usual severity vomiting C0027643 Neoplasm recurrence, local HSDN C2315100 Pediatric failure to thrive C0268193 Nadh cytochrome b5 reductase deficiency MalaCards C4084775 Usual severity weight loss C0019209 Hepatomegaly HSDN C0041657 Consciousness loss C0036341 Schizophrenia HSDN C0018681 Headache, cephalalgia C0019159 Hepatitis a HSDN C0030554 Abnormal sensation C1963198 Pancreatitis adverse event HSDN C4084727 Cough frequency C0041234 Chagas disease OrphaNet|MalaCards C3887784 Decreased urine output C0002351 Altitude sickness HSDN C0271215 Blindness legal C1836544 Schindler disease, type i OrphaNet|MalaCards C0178417 Anhedonia C2707011 Behavioral symptoms:-:point in time:^patient:- HSDN C2911645 Weight loss adverse event C0013363 Dysautonomia HSDN C0917816 Deficiency mental C1857776 3-@methylglutaconic aciduria, type v MalaCards|HPO C4084784 Diarrhea C0005417 Bile duct fistula HSDN C0033377 Caudal displacement C1840528 Holoprosencephaly 4 (disorder) HPO C3274924 Have been coughing C1956390 Cranial arteritis MalaCards C0040822 D tremors C1719788 Episodic ataxia type 1 HPO C0234146 Absent reflex C2752089 Neuropathy, hereditary sensory and autonomic, type iia HPO C0427055 Face weakness C4225368 Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency UMLS C0520909 Ponv C2911643 Encounter due to family history of osteoporosis HSDN C0039070 Collapse fleeting C0021051 Immunologic deficiency syndromes HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035854 Rosacea HSDN C4085210 Usual severity pain C0206721 Inverted papilloma HSDN C0018784 Deafness sensorineural C0013808 Electroconvulsive therapy HSDN C0036572 Convulsion C1270972 Mild cognitive disorder HSDN C3539022 Pelvic pain decreasing in severity C0040053 Thrombosis HSDN C0018991 Paralysis one side of body C1548777 Specimen reject reason - hemolysis HSDN C0013404 Respiratory difficulty C0742290 Chest pain char pleuritic UMLS C4084727 Cough frequency C0276108 Chlamydia infection psittaci HSDN C1963087 Constipation adverse event C0268579 Propionic acidemia OrphaNet|HPO C1963071 Back pain adverse event C2137063 Ent surgical result - speech HSDN C0000737 Abdomen pain C0026766 Multiple organ failure HSDN C4084727 Cough frequency C0005967 Bone neoplasms HSDN C0000737 Abdomen pain C2931758 Acquired angioedema OrphaNet|MalaCards C0040822 D tremors C0026764 Multiple myeloma HSDN C0231528 Muscle pain generalized C0034139 Purine-pyrimidine metabolism, inborn errors HSDN C2242996 Tingling C0022738 Klippel-feil syndrome HSDN C0019825 Voice hoarseness C2981276 Stage iva thyroid gland undifferentiated (anaplastic) carcinoma UMLS C0040264 Ear ringing sound C0017181 Gastrointestinal hemorrhage HSDN C0015402 Hemorrhage eye C1690964 Cataract HSDN C0242936 Center pain C0036631 Seminoma HSDN C0026821 Cramp C0016510 Foot diseases HSDN C0013604 Edematous C0003872 Arthritis, psoriatic HSDN C2984058 Have pain C0025063 Mediastinal neoplasms HSDN C4085661 Usual severity nausea C0008066 Child behavior disorders HSDN C0578739 Popliteal lymph node enlargement C1264170 Superficial popliteal lymphadenopathy UMLS C4084727 Cough frequency C0003467 Anxiety HSDN C0557874 Global developmental delay C0795941 Brachycephaly-deafness-cataract-microstomia-mental retardation syndrome MalaCards C0020673 Hypothermia (central) (local) C0034531 Experimental radiation injuries HSDN C0020672 Body temperature decreased C1963119 Stomach ulcer adverse event HSDN C0851578 Disorder sleep C4049994 Insulin resistance measurement HSDN C0026826 High muscle tone C1275081 Cardio-facio-cutaneous syndrome HPO C2911645 Weight loss adverse event C1855652 Fetus small for gestational age HSDN C0034933 Abnormal reflexes C0008925 Cleft palate HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036631 Seminoma HSDN C0004134 Dyssynergia C3810285 Myopathy with extrapyramidal signs MalaCards C1279888 Proteinuria of undiagnosed cause C0221204 Lytic lesion MalaCards C0034150 Skin purpura C0001622 Adrenal gland hyperfunction OrphaNet C4042891 Sleep wake disorders C0009651 Conditioning operant HSDN C0221232 Welts C1304198 Episodic angio-oedema with eosinophilia UMLS C3539023 Pelvic pain increasing in frequency C1962963 Osteoporosis adverse event HSDN C0016382 Cutaneous vascular engorgement C0001624 Adrenal gland neoplasms HSDN C0040264 Ear ringing sound C0037304 Skull fracture HSDN C0749851 Upper extremity tingling C0745881 Lower extremity paresthesia tingling UMLS C0030193 Sense of pain C2936631 Complaint, subjective health HSDN C0242936 Center pain C0022610 Kernicterus HSDN C4085862 Bothered by nausea C0022116 Ischemia HSDN C3641756 Have diarrhea C0042267 Vaginitis HSDN C1963184 Nystagmus adverse event C3150675 Chromosome 15q24 duplication syndrome HPO C0007642 Cellulitis nos C3887645 Job syndrome HPO C0013404 Respiratory difficulty C1547046 Kind of quantity - taste HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006309 Brucellosis HSDN C0518090 Frequency of pain question C1963266 Uveitis adverse event HSDN C0036572 Convulsion C0020681 Sleep-related respiratory failure MalaCards C4084768 Usual severity vomiting C0004030 Aspergillosis HSDN C0042024 Urine incontinence C1956346 Coronary artery disease HSDN C1069915 Vertigo C0518450 Spinal fractures HSDN C0013604 Edematous C1322286 Thymoma, type c OrphaNet|MalaCards C0004310 Auditory disorder process C0752322 Epilepsy, partial, sensory HSDN C1963281 Vomiting adverse event C0338480 Common migraine HSDN C4085642 Level of joint stiffness C0268263 Multiple sulfatase deficiency disease OrphaNet|HPO|MalaCards C2984058 Have pain C2073625 X-ray of chest: pleural effusion HSDN C0013404 Respiratory difficulty C0494491 Mononeuropathies HSDN C0575081 Abnormal gait C0265279 Kniest dysplasia MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0013264 Muscular dystrophy, duchenne HSDN C0009806 Constipate C0032344 Poisoning aspects HSDN C0009421 Comatose C0520680 Sleep apnea, central HSDN C0020578 Hyperventilate C0007020 Carbon monoxide poisoning HSDN C0033774 Skin pruritus C0022660 Kidney failure, acute HSDN C4084775 Usual severity weight loss C0029410 Osteoarthritis of hip HSDN C2911647 Weight gain adverse event C0014859 Esophageal neoplasms HSDN C0037763 Spasm C0012746 Dissociative disorder HSDN C1963091 Diarrhea adverse event C0039128 Syphilis HSDN C2169806 Tic C0393593 Dystonia disorders HSDN C1069915 Vertigo C0428977 Bradycardia HSDN C0023012 Delay language C1845543 Mental retardation, x-linked, with epilepsy MalaCards|HPO C0007758 Cerebellar ataxia C0950123 Inborn genetic disease HSDN C2984058 Have pain C0013010 Cerebral lateralization HSDN C0036659 Sensation disorder C0029172 Oral submucous fibrosis HSDN C3541349 Syncope C1261473 Sarcoma HSDN C0423715 Testicular neuralgia C0553760 Lumbosacral plexus neuropathy UMLS C0040485 Wryneck C0037369 Smoking HSDN C0020578 Hyperventilate C0040053 Thrombosis HSDN C0034124 Pupillary disorder C0520680 Sleep apnea, central HSDN C4084767 Bothered by vomiting C0036864 Sexual relations HSDN C0038002 Spleen enlargement C3150354 Immunodeficiency, common variable, 2 MalaCards|HPO C4084775 Usual severity weight loss C0085298 Sudden cardiac death HSDN C3541349 Syncope C1859062 Long qt syndrome 3 HPO C2237041 Shox gene with short stature C3150874 Cranioectodermal dysplasia 2 MalaCards C0036572 Convulsion C0085261 Proteus syndrome HPO C0016382 Cutaneous vascular engorgement C0428953 Ecg infarction myocardial HSDN C2242996 Tingling C0030481 Tropical spastic paraparesis HSDN C2108785 Joint pain in right middle toe worsens while standing C1861963 Camptobrachydactyly MalaCards C1549543 Administration method - pain C0008495 Chorioamnionitis HSDN C2237041 Shox gene with short stature C1856054 Hutterite cerebroosteonephrodysplasia syndrome MalaCards C4084774 Have weight loss C0263666 Dermatomyositis, childhood type MalaCards C0557874 Global developmental delay C0265286 Dyggve-melchior-clausen syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C1850597 Leigh syndrome due to mitochondrial complex ii deficiency HPO C0036572 Convulsion C0085436 Meningitis, cryptococcal HSDN C0022346 Yellow skin C0032371 Poliomyelitis HSDN C0024031 Back pain lower back C2073625 X-ray of chest: pleural effusion HSDN C0037316 Not enough sleeping C0034040 Puerperal disorders HSDN C1557397 Adverse event associated with pain C0376670 Pancreatitis, alcoholic HSDN C1963180 Neck pain adverse event C0700327 Clinical findings relating to memory HSDN C0231528 Muscle pain generalized C0398691 Hyperimmunoglobulinemia d OrphaNet|HPO|MalaCards C0917801 Sleep disorder insomnia C0393758 Persistent insomnia UMLS C0002962 Angina C0263666 Dermatomyositis, childhood type MalaCards C0042024 Urine incontinence C0027819 Neuroblastoma HSDN C4084773 Bothered by weight gain C0032273 Pneumoconiosis HSDN C3898969 Have been vomiting C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C0030193 Sense of pain C0007279 Carotid body paraganglioma HSDN C4084784 Diarrhea C0872315 Communicable diseases emerging HSDN C3898969 Have been vomiting C0004626 Pneumonia, bacterial HSDN C0020455 Hypergammaglobulinemia C0028817 Ochronosis HSDN C0019572 Hairiness C0022927 Disorder of lactation HSDN C0013604 Edematous C0019569 Hirschsprung disease HSDN C0917816 Deficiency mental C1861178 Thrombocytopenia paris-trousseau type OrphaNet|HPO|MalaCards C0026821 Cramp C0034139 Purine-pyrimidine metabolism, inborn errors HSDN C0010200 Cough symptom C0042111 Urticaria pigmentosa MalaCards C1549543 Administration method - pain C0018789 Cardiac aneurysm HSDN C0013362 Dysarthrias C0751603 Autosomal recessive hereditary spastic paraplegia MalaCards C4084774 Have weight loss C2984330 Chagas disease pathway HSDN C0030193 Sense of pain C1515868 Acinic cell breast carcinoma UMLS C4084775 Usual severity weight loss C0006105 Brain abscess HSDN C0036572 Convulsion C4274731 Jeavons syndrome UMLS C0018772 Deafness C3809526 Combined oxidative phosphorylation deficiency 17 MalaCards C0018784 Deafness sensorineural C1556682 Adverse event associated with infection HSDN C0042024 Urine incontinence C1579931 Depressed - symptom HSDN C1963091 Diarrhea adverse event C2931067 Cholestasis, progressive familial intrahepatic 4 MalaCards C0027497 Queasy C0036341 Schizophrenia HSDN C0030193 Sense of pain C1336427 Stage iv carcinoma of nasal cavity UMLS C4084784 Diarrhea C0037930 Spinal cord neoplasms HSDN C4085210 Usual severity pain C0024689 Mandibular diseases HSDN C4084767 Bothered by vomiting C3539615 Nci ctep sdc gestational trophoblastic disease sub-category terminology HSDN C0267028 Lip pain C0267033 Lip ulcer UMLS C0033377 Caudal displacement C0263627 Calcinosis universalis OrphaNet|HPO C0027066 Myoclonic jerking C0041327 Tuberculosis, pulmonary HSDN C0424755 Fever symptoms C0600518 Choroidal neovascularization HSDN C0036659 Sensation disorder C0025281 Meniere disease HSDN C0008031 Pain chest C1333069 Clear cell carcinoma of thymus UMLS C3814530 Skin vesicle C0162569 Hepatoerythropoietic porphyria MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0238198 Gastrointestinal stromal tumors HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023348 Leprosy, lepromatous HSDN C0013604 Edematous C0027868 Neuromuscular diseases HSDN C1145670 Failure respiratory C0238052 Xanthomatosis, cerebrotendinous MalaCards|HPO C0009806 Constipate C0149770 Rectal abscess UMLS C0040264 Ear ringing sound C0428953 Ecg infarction myocardial HSDN C4085211 Pain distress question C0009782 Connective tissue diseases HSDN C0013604 Edematous C0033586 Failure, prosthesis HSDN C0085593 Chill C0016514 Foot-and-mouth disease HSDN C1963093 Dizziness adverse event C0038587 Substance withdrawal syndrome HSDN C4084788 Have dizziness C0006840 Candidiasis HSDN C3827868 Tachycardia by ecg finding C3149848 Variegate porphyria, homozygous variant HPO C0004093 Asthenia C0041296 Tuberculosis HSDN C0454644 Delayed language development C0015393 Eye abnormalities MalaCards C4050613 Anxiety C1847627 Dyskinesia, familial, with facial myokymia MalaCards|HPO C2237041 Shox gene with short stature C2675228 Ciliary dyskinesia, primary, 12 MalaCards|HPO C4085862 Bothered by nausea C0023467 Leukemia, myelocytic, acute HSDN C0232513 Premature tooth loss C0917990 Acro-osteolysis MalaCards C3898969 Have been vomiting C0269291 Pregnancy heterotopic HSDN C0002170 Alopecia disorders C1864826 Epidermolysis bullosa, lethal acantholytic OrphaNet|HPO|MalaCards C0005745 Blepharoptosis C1841696 Macdermot patton williams syndrome MalaCards C4085210 Usual severity pain C0035235 Respiratory syncytial virus infections HSDN C4084724 Usual severity constipation C2717876 Aciduria, propionic OrphaNet|HPO C1963170 Hypothermia adverse event C0025063 Mediastinal neoplasms HSDN C2315100 Pediatric failure to thrive C1865371 Severe combined immunodeficiency, athabaskan-type HPO C0000727 Abdomen acute C0343387 Enterocolitis, neutropenic HSDN C0522179 Anxiety death C0150023 Ineffective denial UMLS C0344434 Atrial fibrillation ecg C3151204 Cardiomyopathy, familial hypertrophic, 16 HPO C1961131 Cough adverse event C0001486 Adenovirus infections HSDN C0040822 D tremors C0038358 Gastric ulcer HSDN C0241210 Speaking delay C1412746 Bbs1 gene HPO C0037763 Spasm C1548777 Specimen reject reason - hemolysis HSDN C0085636 Light sensitivity C1145628 Autonomic nervous system disorders HSDN C4084788 Have dizziness C0600260 Lung diseases, obstructive HSDN C1963091 Diarrhea adverse event C0279607 Adult primary hepatocellular carcinoma MalaCards C1961131 Cough adverse event C1527407 Eosinophilic pneumonia DiseaseOntology C3641756 Have diarrhea C0035235 Respiratory syncytial virus infections HSDN C0270948 Neurogenic muscular atrophy C1856301 Gsd iv, classic hepatic HPO C2024878 Cardiovascular surgery result: dyspnea C0014117 Endocardial fibroelastosis HSDN C0019572 Hairiness C0085132 Mucopolysaccharidosis vii HPO C3887873 Hearing loss C0265354 Charge syndrome HSDN C4084802 Usual severity diarrhea C3151147 Bile acid synthesis defect, congenital, 3 MalaCards|HPO C0026821 Cramp C0342769 Deficiency dehydrogenase lactate MalaCards C0037199 Sinus infection C3809701 Ciliary dyskinesia, primary, 27 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0700359 Organophosphate poisoning HSDN C0242936 Center pain C0001828 Agricultural workers' diseases HSDN C0008031 Pain chest C0023240 Legionellosis OrphaNet|MalaCards C0231341 Aging premature C0010068 Coronary heart disease HSDN C0034155 Thrombotic thrombocytopenic purpura C1706377 Memory device component HSDN C0020458 Hyperhydrosis C1849321 Sandhoff disease, juvenile type HPO C0557874 Global developmental delay C0795949 Galloway mowat syndrome OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0015397 Disorder of eye HSDN C4084767 Bothered by vomiting C1510412 Pseudoaneurysm HSDN C0013604 Edematous C0042769 Virus diseases HSDN C0018681 Headache, cephalalgia C0477379 Drug-induced headache, nec in snomedct UMLS C1961131 Cough adverse event C0042373 Vascular diseases HSDN C0086565 Liver function abnormal C2931038 Pancreatic carcinoma, familial MalaCards C0033377 Caudal displacement C1837475 Insulin-like growth factor i deficiency MalaCards|HPO C0026826 High muscle tone C0013080 Down syndrome HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0428977 Bradycardia HSDN C0242936 Center pain C0034103 Pulpitis HSDN C0013404 Respiratory difficulty C0017107 Gas poison HSDN C0003469 Anxiety disorder C1853833 Parkinson disease 6, autosomal recessive early-onset HPO C1279888 Proteinuria of undiagnosed cause C1854336 Paragangliomas 3 MalaCards C0023014 Developmental disorder language C0018799 Heart diseases HSDN C0577560 Eye mass C0085270 Orbit pseudotumor UMLS C0018681 Headache, cephalalgia C0852795 Increased insulin level HSDN C0011991 Loose stools C0018794 Heart block HSDN C0398650 Idiopathic thrombocytopenia purpura C0007621 Neoplastic cell transformation HSDN C0035232 Diaphragmatic paralysis C0752282 Congenital structural myopathy HSDN C0547030 Sensory perceptual alteration: visual C0042798 Low vision UMLS C0231218 Malaise generalized C1336811 Transplant-related hepatocellular carcinoma UMLS C0019079 Bloody sputum C0700208 Acquired scoliosis HSDN C4085210 Usual severity pain C0013928 Fat embolism HSDN C1963281 Vomiting adverse event C1963211 Pericarditis adverse event HSDN C0728710 Pupil constriction observed C2749346 Refsum disease, adult, 2 HPO C1384666 Decreased hearing C2677434 Orofacial cleft 11 MalaCards C0040259 Tinea pedis C1881674 Medical device emits smoke HSDN C3887873 Hearing loss C2004491 Cicatrix HSDN C0349588 Stature short C2751297 Sthag6 MalaCards|HPO C0037316 Not enough sleeping C0032962 Pregnancy complications HSDN C0002170 Alopecia disorders C0079154 Congenital nonbullous ichthyosiform erythroderma OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0010074 Coronary vessel anomalies HSDN C0004604 Pain back C0458219 Complex regional pain syndromes HSDN C0042024 Urine incontinence C0241158 Cicatrix skin HSDN C2911647 Weight gain adverse event C0037753 Sparganosis HSDN C4084767 Bothered by vomiting C0007932 Chagas' disease + no organ inv DiseaseOntology C0027497 Queasy C0038454 Cerebrovascular accident HSDN C0349588 Stature short C3150803 Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia MalaCards|HPO C0004604 Pain back C0010356 Cross infection HSDN C0349588 Stature short C2674937 Chromosome 10q26 deletion syndrome MalaCards C0151786 Weakness muscle C0020458 Hyperhidrosis disorder HSDN C4084802 Usual severity diarrhea C0003125 Anorexia nervosa HSDN C0751495 Seizure focal C0270849 Extratemporal epilepsy UMLS C1963071 Back pain adverse event C0023801 Lipomatosis HSDN C0011991 Loose stools C0027627 Neoplasm metastasis HSDN C0518090 Frequency of pain question C0021832 Intestinal diseases, parasitic HSDN C2984058 Have pain C0027121 Myositis HSDN C0043094 Weight gain C0024236 Lymphedema HSDN C0018784 Deafness sensorineural C1837007 Deafness, autosomal recessive 36, with or without vestibular involvement HPO C0019209 Large liver C2931872 Free sialic acid storage disease MalaCards C4084768 Usual severity vomiting C0349231 Phobic anxiety disorder HSDN C4085211 Pain distress question C0040799 Traumatic subcutaneous emphysema HSDN C1000483 Genus anemia C1832529 Hereditary hemorrhagic telangiectasia-related pulmonary arterial hypertension HPO C0033774 Skin pruritus C0079583 Ichthyosiform erythroderma, congenital MalaCards C4085210 Usual severity pain C0878588 Sphincter oddi dysfunction HSDN C3541349 Syncope C0027902 Neuropsychological diagnosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0005639 Bisexual behavior HSDN C0015469 Facial paralysis C0026650 Movement disorders HSDN C4084723 Constipation C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C0009806 Constipate C0031873 Pica disease HSDN C3274924 Have been coughing C0007222 Cardiovascular diseases HSDN C0426579 Anorexia symptom C0018249 Grooming HSDN C0567522 Nipple discharge - pus C0745283 Infectious process UMLS C1961131 Cough adverse event C0149931 Migraine disorders HSDN C0005779 Clotting C0015519 Factor x deficiency MalaCards C0184567 Pain acute C3850024 Transcranial direct current stimulation HSDN C4085641 Level of joint pain C1838429 Epiphyseal dysplasia, multiple, 2 MalaCards C0002962 Angina C0038436 Post-traumatic stress disorder HSDN C0242936 Center pain C0004099 Asthma, exercise-induced HSDN C0018991 Paralysis one side of body C2034128 Paralysis of unknown etiology UMLS C0013404 Respiratory difficulty C0017531 Angiolymphoid hyperplasia HSDN C0151786 Weakness muscle C1553188 Hemolysis - observation HSDN C1549543 Administration method - pain C0085399 Ehrlichiosis HSDN C1963281 Vomiting adverse event C0029118 Opportunistic infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006666 Calciphylaxes HSDN C0344315 Mood depressed C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0018621 Hay fever HSDN C0557874 Global developmental delay C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C0151311 Cranial nerve palsy C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C0917816 Deficiency mental C1291512 Beta-ureidopropionase deficiency MalaCards|HPO C0030200 Intractable pain C0004096 Asthma HSDN C0013604 Edematous C0282102 Chondrodysplasia punctata, x-linked dominant type HPO C0037317 Sleep disturbance C0270958 Kocher-debre-semelaigne syndrome OrphaNet|MalaCards C1959630 Eye pain adverse event C1704421 Skin pigmentation disorder HSDN C0033774 Skin pruritus C0039730 Thalassemia HSDN C3463815 Feel fatigue C0178573 Behavior criminal HSDN C3146279 Coma C0037933 Spinal diseases HSDN C1145670 Failure respiratory C0036421 Systemic scleroderma OrphaNet|MalaCards C0851578 Disorder sleep C0035334 Retinitis pigmentosa HSDN C0015672 Decreased energy C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C2024893 Cardiovascular surgery result: fatigue C0037997 Splenic diseases HSDN C4084726 Distress cough C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0037771 Paraparesis spastic C0752180 Bacterial cns infection HSDN C0015672 Decreased energy C0020635 Hypopituitarism HSDN C2911645 Weight loss adverse event C0033906 Psychological theories HSDN C1519353 Skin eruption papular C0019618 Histiocytosis MalaCards C4084723 Constipation C0001403 Addison disease OrphaNet C3463815 Feel fatigue C0018767 Auditory sense HSDN C3815497 Cough C0025289 Meningitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0041755 Adverse reaction to drug HSDN C0030794 Pelvis pain C0019294 Hernia, inguinal HSDN C3665347 Vision impaired C0265376 Fetal methyl mercury syndrome OrphaNet C4085317 Diarrhea frequency C0012691 Dislocations HSDN C1557397 Adverse event associated with pain C1956418 Torsion abnormality HSDN C0043094 Weight gain C0007222 Cardiovascular diseases HSDN C4042891 Sleep wake disorders C0020443 Hypercholesterolemia HSDN C0030193 Sense of pain C0013884 Filarial elephantiases HSDN C0026884 Muteness C2931366 Congenital deformity of the thumb and congenital alopecia MalaCards C4084725 Usual severity cough C0015302 External exotoses HSDN C0023012 Delay language C4014700 Encephalopathy, progressive, with or without lipodystrophy MalaCards C0033790 Pseudobulbar palsy C0751955 Brain infarction HSDN C3539022 Pelvic pain decreasing in severity C0242669 Placenta retained HSDN C4084766 Vomiting C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C0030554 Abnormal sensation C0010308 Congenital hypothyroidism MalaCards C1963063 Anorexia adverse event C0236969 Substance-related disorders HSDN C3641755 Have constipation C0023895 Liver diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036920 Sezary syndrome HSDN C0008031 Pain chest C0023903 Liver neoplasms HSDN C0030200 Intractable pain C0003873 Rheumatoid arthritis HSDN C0000737 Abdomen pain C1444838 Chronic arthritis of juvenile onset OrphaNet C3829611 Nausea frequency C0001624 Adrenal gland neoplasms HSDN C0036659 Sensation disorder C0010674 Cystic fibrosis HSDN C0030552 Paralysis partial C0037199 Sinusitis HSDN C0009676 Confusion state C0024305 Lymphoma, non-hodgkin HSDN C4084802 Usual severity diarrhea C0206526 Tuberculosis, multidrug-resistant HSDN C0011991 Loose stools C0016057 Fibrosarcoma HSDN C0004604 Pain back C0029401 Osteitis deformans HSDN C2919142 Short stature adverse event C0079583 Ichthyosiform erythroderma, congenital MalaCards C0022346 Yellow skin C0342191 Familial dyshormonogenetic goiter MalaCards C4084766 Vomiting C0017658 Glomerulonephritis HSDN C3815497 Cough C0342257 Complications of diabetes mellitus HSDN C4084768 Usual severity vomiting C0035457 Rhinitis, allergic, perennial HSDN C4084769 Vomiting frequency C0031069 Familial mediterranean fever HSDN C4085317 Diarrhea frequency C0393735 Headache disorders HSDN C2985303 Late pregnancy bleeding C0032962 Pregnancy complications UMLS C4084766 Vomiting C0018818 Ventricular septal defects HSDN C3463815 Feel fatigue C2609414 Acute kidney injury HSDN C0007758 Cerebellar ataxia C0752123 Spinocerebellar ataxia type 5 UMLS C4085210 Usual severity pain C0080040 Polio post syndrome MalaCards C0042963 Symptoms vomiting C0206644 Histiocytoma, benign fibrous HSDN C0241210 Speaking delay C2931338 Chromosome 3, monosomy 3q13 MalaCards C0033774 Skin pruritus C0002994 Angioedema HSDN C0018777 Deafness, conductive C2748918 Otopalatodigital spectrum disorder HPO C0038002 Spleen enlargement C0342853 Sialuria MalaCards|HPO C0085593 Chill C0020625 Hyponatremia UMLS C0020672 Body temperature decreased C0007453 Cattle disease HSDN C4084776 Weight loss C0024205 Lymphadenitis HSDN C3541349 Syncope C0011616 Contact dermatitis HSDN C0518090 Frequency of pain question C0035086 Renal osteodystrophy HSDN C1963093 Dizziness adverse event C0023418 Leukemia HSDN C2203646 Jaundice C0020428 Hyperaldosteronism HSDN C0410919 Foetal bradycardia C2118397 Fetal bradycardia before onset of labor UMLS C1549543 Administration method - pain C1253937 Pericardial effusion HSDN C0270948 Neurogenic muscular atrophy C0270914 Hereditary motor and sensory-neuropathy type ii OrphaNet|HPO C1963086 Confusion adverse event C0005695 Bladder neoplasm HSDN C0019079 Bloody sputum C0041909 Gastrointestinal bleed upper UMLS C0030193 Sense of pain C0080032 Pleural effusion, malignant HSDN C0007758 Cerebellar ataxia C0024003 Lordosis HSDN C0013395 Indigestion C0262655 Recurrent urinary tract infection HSDN C0039070 Collapse fleeting C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0015468 Face pain C0362076 Head problem UMLS C0151786 Weakness muscle C1260409 Myasthenia gravis without acute exacerbation MalaCards C0237326 Defecation pain C0300948 Caudal regression syndrome HPO C0023012 Delay language C0796249 Mental retardation, x linked 47 HPO C1963252 Tremor adverse event C2930815 Acute cerebral gaucher disease MalaCards C2024878 Cardiovascular surgery result: dyspnea C0032914 Pre-eclampsia HSDN C0008031 Pain chest C0016045 Fibroma HSDN C0036572 Convulsion C2930927 Kallmann syndrome, type 3, recessive MalaCards C0030975 Disorders perception C0018916 Hemangioma HSDN C0085632 Listlessness C4225326 Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 UMLS C0020580 Decreased sensation C0022116 Ischemia HSDN C0007398 Catatonic C0019693 Hiv infections HSDN C0036572 Convulsion C0234538 Puerperal convulsion UMLS C0426579 Anorexia symptom C0003838 Arterial occlusive diseases HSDN C0041834 Erythematous condition C1833030 Palmoplantar keratoderma, nonepidermolytic OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C0031190 Persistent fetal circulation syndrome HSDN C4084723 Constipation C1704272 Benign prostatic hyperplasia HSDN C2984058 Have pain C0339946 Pulmonary tularemia DiseaseOntology C0015230 Exanthem C0221013 Mastocytosis, systemic OrphaNet|MalaCards C1963091 Diarrhea adverse event C0039981 Thoracic neoplasms HSDN C0424755 Fever symptoms C0036875 Disorders of sex development HSDN C3539895 Pelvic pain occurs with bowel movement C0022661 Kidney failure, chronic HSDN C1069915 Vertigo C0029401 Osteitis deformans HSDN C2108112 Continuous electrocardiogram ventricular fibrillation C3501851 Long qt syndrome 2-5 MalaCards C0030552 Paralysis partial C0019829 Hodgkin disease HSDN C3541349 Syncope C0008350 Cholelithiasis HSDN C0010200 Cough symptom C0154070 Carcinoma in situ of trachea UMLS C0151686 Growth retardation C1837371 Sudden infant death with dysgenesis of the testes syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0020458 Hyperhidrosis disorder HSDN C3463815 Feel fatigue C0032066 Plague vaccines HSDN C0013421 Dystonia C2677682 Rett syndrome, zappella variant HPO C1549543 Administration method - pain C0001144 Acne vulgaris HSDN C0522224 Palsied C0393639 Hashimoto's encephalitis OrphaNet|MalaCards C4084766 Vomiting C0752165 Angioma, venous, central nervous system HSDN C1000483 Genus anemia C0268390 Muckle-wells syndrome MalaCards|HPO C0030552 Paralysis partial C0265326 Bannayan-riley-ruvalcaba syndrome MalaCards C3539895 Pelvic pain occurs with bowel movement C0022865 Obstetric labor complications HSDN C4084776 Weight loss C0043097 Perception, weight HSDN C0522224 Palsied C0039131 Syphilis congenital HSDN C0022346 Yellow skin C3489413 Lipomatosis, multiple HSDN C4042891 Sleep wake disorders C3541306 Plasmodium measurement HSDN C0009806 Constipate C0002871 Anemia HSDN C0004604 Pain back C0263888 Back disorder UMLS C0041657 Consciousness loss C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0025222 Melena HSDN C0000737 Abdomen pain C2987189 Itpn UMLS C1963064 Anxiety adverse event C0242526 Gonadal dysgenesis, 45,x OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0022134 Islet cell adenoma HSDN C1963063 Anorexia adverse event C0153463 Malig neop oth spec pancreas MalaCards C0000727 Abdomen acute C0038565 Subphrenic abscess HSDN C0007758 Cerebellar ataxia C0027145 Myxedema HSDN C1963064 Anxiety adverse event C0162531 Hereditary coproporphyria OrphaNet|HPO C0040264 Ear ringing sound C0029888 Otitis media purulent HSDN C0026821 Cramp C0024141 Lupus erythematosus, systemic HSDN C0018772 Deafness C1319466 Barber say syndrome OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0021361 Female infertility HSDN C0034155 Thrombotic thrombocytopenic purpura C0085655 Polymyositis HSDN C0015970 Fever unknown origin C1510428 Cerebral abscess HSDN C2242996 Tingling C0003803 Arnold chiari malformation HSDN C0020672 Body temperature decreased C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C4085210 Usual severity pain C0001824 Agranulocytosis HSDN C0018681 Headache, cephalalgia C1705810 Generic role HSDN C0036572 Convulsion C0014534 Epididymitis HSDN C1961131 Cough adverse event C0040128 Thyroid diseases HSDN C1963170 Hypothermia adverse event C1962983 Cataract adverse event HSDN C0155016 Blindness color green red C0338508 Optic atrophy, autosomal dominant MalaCards|HPO C0152169 Colic renal C0022656 Kidney cortex necrosis HSDN C2984058 Have pain C0022680 Polycystic kidney diseases HSDN C0013395 Indigestion C0162526 Aids-related opportunistic infections HSDN C0039070 Collapse fleeting C0037019 Shy-drager syndrome HSDN C2203646 Jaundice C0021890 Intraoperative complications HSDN C0020673 Hypothermia (central) (local) C1527311 Brain edema HSDN C4084768 Usual severity vomiting C0015414 Eye neoplasms HSDN C2237041 Shox gene with short stature C1148551 X-linked dyskeratosis congenita MalaCards|HPO C3463815 Feel fatigue C1704436 Peripheral arterial diseases HSDN C4084725 Usual severity cough C0032131 Plasmacytoma HSDN C0398650 Idiopathic thrombocytopenia purpura C4084909 Depression subordinate domain HSDN C0020505 Excessive eating C0014371 Enterotoxemia HSDN C0349588 Stature short C1842687 Pontocerebellar hypoplasia type 3 (disorder) MalaCards|HPO C1963086 Confusion adverse event C0001529 Dercum disease HSDN C3539020 Pelvic pain decreasing in frequency C0011854 Diabetes mellitus, insulin-dependent HSDN C0751093 Dystonia, limb C2751067 Parkinsonism-dystonia, infantile MalaCards|HPO|UMLS C0010200 Cough symptom C0220847 C hepatitis virus HSDN C1384666 Decreased hearing C0796059 Oculopalatoskeletal syndrome MalaCards C1963252 Tremor adverse event C0268407 Senile cardiac amyloidosis MalaCards C1963091 Diarrhea adverse event C0032066 Plague vaccines HSDN C0349588 Stature short C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0085593 Chill C0029835 Other specified tularemia nos DiseaseOntology|MalaCards C1963184 Nystagmus adverse event C3164344 Adult onset autosomal dominant leukodystrophy OrphaNet|HPO C0013595 Eczematous dermatitis C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C1963093 Dizziness adverse event C0041327 Tuberculosis, pulmonary HSDN C0002962 Angina C0162869 Aneurysm, ruptured HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0024788 Green monkey virus disease DiseaseOntology|OrphaNet|MalaCards C0022346 Yellow skin C0033677 Protein-energy malnutrition HSDN C3641756 Have diarrhea C0023646 Lichen planus HSDN C4085661 Usual severity nausea C0032087 Plant poisoning HSDN C1963063 Anorexia adverse event C1961835 Gaucher disease, type 1 OrphaNet|HPO|MalaCards C0344315 Mood depressed C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0027066 Myoclonic jerking C0001624 Adrenal gland neoplasms HSDN C2919142 Short stature adverse event C1862151 Brachydactyly, type a1 (disorder) OrphaNet|HPO|MalaCards C2984058 Have pain C0027947 Neutropenia HSDN C0036572 Convulsion C3179455 Niemann-pick disease, type c1 MalaCards|HPO|UMLS C0018681 Headache, cephalalgia C0004659 Bacteriuria HSDN C0557874 Global developmental delay C3809844 Chromosome 22q13 duplication syndrome MalaCards C2984058 Have pain C0032708 Disorders of porphyrin metabolism HSDN C1557397 Adverse event associated with pain C0018994 Hemobilia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1705812 Nci thesaurus role HSDN C0018784 Deafness sensorineural C1969607 Kallmann syndrome 2 with selective tooth agenesis HPO C1827358 Gait dyspraxia C0003635 Apraxias UMLS C2315100 Pediatric failure to thrive C0220708 Vater association MalaCards|HPO C0151786 Weakness muscle C0206725 Subependymal glioma HSDN C4085862 Bothered by nausea C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4085210 Usual severity pain C0029434 Osteogenesis imperfecta HSDN C4085862 Bothered by nausea C0027092 Myopia HSDN C0018780 Frequencies hearing high loss C0043207 Wolfram syndrome HSDN C4084776 Weight loss C0036323 Schistosomiasis HSDN C0231712 Gait waddling C2930900 Beta-sarcoglycanopathy MalaCards C0000737 Abdomen pain C0043541 Zygomycoses HSDN C0000737 Abdomen pain C0014324 Entamoebiasis HSDN C4084767 Bothered by vomiting C0003869 Arthritis, infectious HSDN C2132198 Abnormal blistering of the skin C0795974 Hereditary macular epidermolysis bullosa OrphaNet C4085210 Usual severity pain C0022729 Klebsiella infections HSDN C0000737 Abdomen pain C0039128 Syphilis HSDN C0036659 Sensation disorder C0262584 Carcinoma, small cell HSDN C0009806 Constipate C1855923 Hyperphosphatasia with mental retardation MalaCards|HPO C1963091 Diarrhea adverse event C0162494 Pregnancy complications, parasitic HSDN C0018991 Paralysis one side of body C0023895 Liver diseases HSDN C1963091 Diarrhea adverse event C0016169 Pathologic fistula HSDN C1549543 Administration method - pain C0006271 Bronchiolitis HSDN C0042420 Vasovagal episode C0556520 Psychological desensitization HSDN C0241165 Skin thickening C0473586 Michelin tire baby syndrome OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0006105 Brain abscess HSDN C0151786 Weakness muscle C0268414 Hyperphosphatasemia with bone disease MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0262655 Recurrent urinary tract infection HSDN C1962972 Proteinuria adverse event C0005686 Urinary bladder diseases HSDN C0018784 Deafness sensorineural C1567742 Alport syndrome, x-linked HPO C0018926 Emesis bloody C0010635 Cystadenoma, mucinous HSDN C0036572 Convulsion C0039504 Injuries tendon HSDN C0162298 Stiffness joints C1855772 Absent corpus callosum cataract immunodeficiency MalaCards|HPO C4085317 Diarrhea frequency C0268124 Adenosine deaminase deficiency MalaCards C0036572 Convulsion C1299262 Sarcoma - category (morphologic abnormality) HSDN C0242936 Center pain C0241158 Cicatrix skin HSDN C0013390 Cramps menstrual C0270611 Brain damage HSDN C0008031 Pain chest C0025064 Mediastinitis HSDN C0042963 Symptoms vomiting C0014836 Escherichia coli infections HSDN C3641756 Have diarrhea C1833454 Komuragaeri disease MalaCards C0242936 Center pain C0017128 Fistula gastric HSDN C4085210 Usual severity pain C0162566 Porphyria cutanea tarda HSDN C2096293 Ent surgical result ear vertigo C0030353 Papilledema HSDN C1557397 Adverse event associated with pain C0013124 Behavior drinking HSDN C0018524 Hallucinate C0162871 Aortic aneurysm, abdominal HSDN C2700617 Irritation - emotion C0266526 Norrie disease OrphaNet|HPO|MalaCards C4085549 Dizziness C0034069 Pulmonary fibrosis HSDN C0028961 Urine output decreased C0085083 Ovarian hyperstimulation syndrome HSDN C0917816 Deficiency mental C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C0007815 Cerebrospinal fluid rhinorrhoea C0013449 Ear neoplasms HSDN C0036659 Sensation disorder C0027889 Hereditary sensory and autonomic neuropathies HSDN C1145670 Failure respiratory C0238027 Botulism, infantile MalaCards C0241210 Speaking delay C3150127 Bardet biedl syndrome 15 HPO C0018965 Blood urine C0034155 Purpura, thrombotic thrombocytopenic MalaCards|HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026636 Mouth diseases HSDN C0426579 Anorexia symptom C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C0036572 Convulsion C1956258 Familial thrombotic thrombocytopenic purpura MalaCards C0011991 Loose stools C0086647 Mucopolysaccharidosis type iiia HPO|UMLS C0033377 Caudal displacement C1834014 Oculopharyngodistal myopathy MalaCards C0018772 Deafness C0796133 Ramon syndrome MalaCards C0009806 Constipate C1707440 Colorectal signet ring cell carcinoma UMLS C0815336 Edema or excessive weight gain in pregnancy, without mention of hypertension, antepartum condition or complication C0156723 Other complications of pregnancy UMLS C0518090 Frequency of pain question C0014236 Endophthalmitis HSDN C0025287 Meningitis-like C0007766 Intracranial aneurysm HSDN C3274924 Have been coughing C0042487 Venous thrombosis HSDN C0042025 Urinary incontinence stress C0026769 Multiple sclerosis HSDN C0234428 Consciousness disturbance C0342443 Adrenal cushing's syndrome MalaCards C0518090 Frequency of pain question C0041107 Trisomy HSDN C2032396 Pelvic pain on the right C0010356 Cross infection HSDN C0007859 Pain neck C0302148 Blood clot HSDN C0018772 Deafness C0008097 Child gifted HSDN C0011991 Loose stools C0311375 Arsenic poisoning HSDN C2700617 Irritation - emotion C0035934 Rubinstein-taybi syndrome OrphaNet|MalaCards C0027066 Myoclonic jerking C1868596 Atypical parkinson disease HPO C2984058 Have pain C0751651 Mitochondrial diseases HSDN C0034155 Thrombotic thrombocytopenic purpura C0018798 Congenital heart defects HSDN C0575081 Abnormal gait C3839326 Kuskokwim syndrome MalaCards C0006370 Bulimia C0001818 Agoraphobia HSDN C3665346 Loss sight C0265321 Wyburn-mason syndrome OrphaNet|MalaCards C3641755 Have constipation C0242698 Ventricular dysfunction, left HSDN C1963281 Vomiting adverse event C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C0019209 Large liver C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii OrphaNet|HPO|MalaCards C0036572 Convulsion C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C4084768 Usual severity vomiting C0018273 Growth disorders HSDN C0231218 Malaise generalized C1333308 Carcinoma of distal biliary tract UMLS C0030193 Sense of pain C2021655 Transvaginal ultrasound: anencephaly of fetus HSDN C0851578 Disorder sleep C2936631 Complaint, subjective health HSDN C1962972 Proteinuria adverse event C0041328 Renal tuberculosis HSDN C3541349 Syncope C1334698 Meningothelial cell neoplasm MalaCards C0700078 Deep tendon reflex decrease C1850303 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive HPO C4085210 Usual severity pain C0016412 Folic acid deficiency HSDN C0917816 Deficiency mental C2936346 22q11 deletion syndrome MalaCards C3829611 Nausea frequency C0009062 Clostridia infection HSDN C2237041 Shox gene with short stature C1852752 Coloboma of macula with type b brachydactyly MalaCards C0036572 Convulsion C0008372 Intrahepatic cholestasis HSDN C0000737 Abdomen pain C0033871 Psychiatric status rating scales HSDN C0042420 Vasovagal episode C0003469 Anxiety disorders HSDN C0237326 Defecation pain C1846058 Lubs x-linked mental retardation syndrome HPO C3539891 Pelvic pain to the rear C0037929 Spinal cord injuries HSDN C1279888 Proteinuria of undiagnosed cause C0600518 Choroidal neovascularization HSDN C0040485 Wryneck C2984299 Asthma pathway HSDN C2984058 Have pain C0010038 Corneal opacity HSDN C2911645 Weight loss adverse event C0032914 Pre-eclampsia HSDN C3665347 Vision impaired C0268263 Multiple sulfatase deficiency disease OrphaNet|HPO|MalaCards C0016199 Pain flank C0206643 Neoplasms, fibrous tissue HSDN C3641755 Have constipation C0027059 Myocarditis HSDN C0009421 Comatose C0019202 Hepatolenticular degeneration MalaCards|HPO C1962962 Hyperpigmentation adverse event C3160739 Fanconi anemia, complementation group e MalaCards C1069915 Vertigo C0042373 Vascular diseases HSDN C2911645 Weight loss adverse event C0020542 Pulmonary hypertension HSDN C0026821 Cramp C0936215 Vitamin b 6 deficiency HSDN C1000483 Genus anemia C2239176 Liver carcinoma MalaCards C0030552 Paralysis partial C1704272 Benign prostatic hyperplasia HSDN C0007758 Cerebellar ataxia C0027877 Neuronal ceroid-lipofuscinoses MalaCards|HSDN C0036572 Convulsion C2677109 Leukodystrophy, hypomyelinating, 4 MalaCards|HPO|UMLS C0039870 Leanness C1090821 Sepsis (invertebrate) HSDN C0008031 Pain chest C1708954 Mediastinal germ cell tumor with somatic-type malignancy UMLS C1279888 Proteinuria of undiagnosed cause C0030920 Peptic ulcer HSDN C4084769 Vomiting frequency C1962958 Hematoma adverse event HSDN C0349588 Stature short C0406727 Orofaciodigital syndrome 4 MalaCards|HPO C0221263 Cafe au lait spot C0032357 Poland syndrome HSDN C2237041 Shox gene with short stature C2931783 Amelogenesis imperfecta nephrocalcinosis MalaCards C0151686 Growth retardation C2751643 Glycogen storage disease ixc MalaCards|HPO C2242996 Tingling C0029134 Optic neuritis HSDN C0030193 Sense of pain C0019542 Higher nervous activity HSDN C2024893 Cardiovascular surgery result: fatigue C1848561 Methylmalonic acidemia with homocystinuria OrphaNet|MalaCards C3641756 Have diarrhea C0162869 Aneurysm, ruptured HSDN C2984058 Have pain C0242994 Hantavirus infections HSDN C0020305 Fetal edema C1969443 Trifunctional protein deficiency with myopathy and neuropathy HPO C4084775 Usual severity weight loss C0026755 Multiple carboxylase deficiency OrphaNet|MalaCards C0005745 Blepharoptosis C3150756 Chromosome 4q21 deletion syndrome MalaCards C0041667 Low weight C0432254 Singleton merten syndrome HPO C0917816 Deficiency mental C0751279 Metachromatic leukodystrophy, adult-type (disorder) HPO C0018926 Emesis bloody C0030305 Pancreatitis HSDN C0030554 Abnormal sensation C0007820 Cerebrovascular disorders HSDN C0023380 Lethargy C0152164 Cyclical vomiting syndrome (disorder) MalaCards|UMLS C0002962 Angina C0037933 Spinal diseases HSDN C0030552 Paralysis partial C0751908 Vestibular neuronitis HSDN C0018784 Deafness sensorineural C0020456 Hyperglycemia HSDN C4085210 Usual severity pain C0036211 Sarcoma 180 HSDN C0020455 Hypergammaglobulinemia C0032227 Pleural effusion disorder HSDN C0040034 Thrombocytopenia C0398641 Epstein syndrome (disorder) HPO C1557397 Adverse event associated with pain C0009353 Colles' fracture HSDN C4085222 Nausea C0005779 Blood coagulation disorders HSDN C1962972 Proteinuria adverse event C0029401 Osteitis deformans HSDN C0557874 Global developmental delay C3542026 Peroxisome biogenesis disorder 5b MalaCards C0013362 Dysarthrias C2931395 Bulbospinal neuronopathy, x-linked recessive HPO C1557397 Adverse event associated with pain C3887650 Adult rickets HSDN C1963091 Diarrhea adverse event C0030469 Paranasal sinus diseases HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0012147 Dientamoebiases DiseaseOntology C0036659 Sensation disorder C0393665 Multiple sclerosis, chronic progressive HSDN C4084724 Usual severity constipation C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C0851578 Disorder sleep C2931673 Ceroid lipofuscinosis, neuronal 1, infantile MalaCards C0151311 Cranial nerve palsy C1762616 Meningioma, benign, no icd-o subtype MalaCards C0023380 Lethargy C0022638 Ketosis HSDN C0151603 Edema generalized C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO C0011168 Disorder deglutition C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C0042024 Urine incontinence C0017152 Gastritis HSDN C1860844 Sparse, thin hair C2677481 Ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency, autosomal dominant HPO C4085549 Dizziness C0030581 Parotid neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0008479 Chondrosarcoma HSDN C4084788 Have dizziness C0026269 Mitral valve stenosis HSDN C4084724 Usual severity constipation C0001807 Aggressive behavior HSDN C0851578 Disorder sleep C0003864 Arthritis HSDN C0242936 Center pain C0020480 Hyperlipoproteinemia type iv HSDN C3463815 Feel fatigue C0003811 Cardiac arrhythmia HSDN C4084727 Cough frequency C0038463 Strongyloides infection HSDN C0162835 Hypopigmentation C0162530 Porphyria, erythropoietic HPO C0700590 Diaphoresis excessive C0040028 Thrombocythemia, essential MalaCards C4084769 Vomiting frequency C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0012546 Diphtheria HSDN C0019825 Voice hoarseness C3810814 Myocardial infarction ecg assessment HSDN C3641756 Have diarrhea C0393735 Headache disorders HSDN C0018991 Paralysis one side of body C0014852 Esophageal diseases HSDN C0036572 Convulsion C3495801 Granulomatosis with polyangiitis MalaCards|HPO C0019521 Hiccoughs C0035229 Respiratory insufficiency HSDN C0557874 Global developmental delay C3554774 Tyshchenko syndrome MalaCards C0848203 Male pelvic pain C2936631 Complaint, subjective health HSDN C4084724 Usual severity constipation C0032266 Emphysema, intestinal HSDN C4084766 Vomiting C0019202 Hepatolenticular degeneration HSDN C4084774 Have weight loss C1527429 Increased blood npn HSDN C3887638 Failure to thrive in infant C2749862 Mitochondrial neurogastrointestinal encephalopathy syndrome, rrm2b-related HPO C0022346 Yellow skin C2981665 Stage ib distal bile duct cancer UMLS C1963087 Constipation adverse event C0007570 Celiac disease DiseaseOntology|HSDN C0162292 Extraocular palsy C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C4084723 Constipation C1866495 Bartter syndrome, antenatal type 1 HPO C0002170 Alopecia disorders C1859133 Rhizomelic chondrodysplasia punctata, type 1 HPO C0009806 Constipate C1704272 Benign prostatic hyperplasia HSDN C4085862 Bothered by nausea C0600260 Lung diseases, obstructive HSDN C4084724 Usual severity constipation C3665624 Serum calcium below normal HSDN C0004604 Pain back C2749106 Emery dreifuss muscular dystrophy 6, x linked MalaCards|HPO C2984058 Have pain C1861172 Venous thromboembolism HSDN C2911645 Weight loss adverse event C1847319 Paraganglioma and gastric stromal sarcoma OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0206138 Crest syndrome MalaCards C0040822 D tremors C0017601 Glaucomas HSDN C0008031 Pain chest C0032285 Pneumonia UMLS C1384666 Decreased hearing C0014038 Encephalitis HSDN C0009792 Consciousness disorder C0006110 Brain death HSDN C0042024 Urine incontinence C0008149 Chlamydia infections HSDN C0004604 Pain back C0004659 Bacteriuria HSDN C1963249 Tinnitus adverse event C0024299 Lymphoma HSDN C0085610 Bradycardia sinus C1833236 Cardiomyopathy, familial hypertrophic, 6 (disorder) HPO C0013394 Coitus painful C3160917 Bladder pain syndrome OrphaNet|MalaCards C0424755 Fever symptoms C0042932 Animal vocalizations HSDN C0042024 Urine incontinence C2713319 Arylsulfatase a deficiency MalaCards C0041657 Consciousness loss C0030492 Parapsychology HSDN C1384666 Decreased hearing C0242383 Age related macular degeneration HSDN C0020615 Hypoglycemia nos C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0030552 Paralysis partial C0021843 Intestinal obstruction HSDN C0030486 Extremity paralysis, lower C0042133 Uterine fibroids HSDN C0027066 Myoclonic jerking C0022797 Adult neuronal ceroid lipofuscinosis OrphaNet|UMLS|MalaCards C0151786 Weakness muscle C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0015970 Fever unknown origin C0031046 Pericarditis HSDN C1963090 Dehydration adverse event C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C0043094 Weight gain C2984291 Glioblastoma multiforme pathway HSDN C0085593 Chill C3163620 Hypotension adverse event HSDN C0041105 Jaw spasm C1837218 Cleft palate, isolated HSDN C4085661 Usual severity nausea C0010674 Cystic fibrosis HSDN C0159040 Skin texture changes C0549660 Other skin disorders UMLS C0018991 Paralysis one side of body C4042784 Feeding and eating disorders HSDN C0042963 Symptoms vomiting C0010692 Cystitis HSDN C4084727 Cough frequency C0040136 Thyroid neoplasm HSDN C4085549 Dizziness C0002940 Aneurysm HSDN C3815497 Cough C0206629 Pulmonary blastoma OrphaNet|HSDN|MalaCards C0085636 Light sensitivity C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C4084773 Bothered by weight gain C0030636 Pasteurella infection HSDN C0037384 Snore C0030567 Parkinson disease HSDN C0042963 Symptoms vomiting C0018482 Haemophilus infections HSDN C1145670 Failure respiratory C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C3829611 Nausea frequency C0007124 Noninfiltrating intraductal carcinoma HSDN C0027066 Myoclonic jerking C3697670 Spinal cord myoclonus UMLS C0349506 Sun sensitivity C0024143 Lupus nephritis MalaCards C0030193 Sense of pain C1963234 Serum sickness adverse event HSDN C0026821 Cramp C0042769 Virus diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0236736 Cocaine-related disorders HSDN C3539022 Pelvic pain decreasing in severity C0019270 Hernia HSDN C3815497 Cough C0017612 Glaucoma, open-angle HSDN C1549543 Administration method - pain C0024919 Behavior, maternal HSDN C4084727 Cough frequency C0003838 Arterial occlusive diseases HSDN C0042928 Paralysis vocal cord C0019693 Hiv infections HSDN C2911647 Weight gain adverse event C0878544 Cardiomyopathies HSDN C0003079 Pupillary inequality C0015393 Eye abnormalities HSDN C0018524 Hallucinate C0243026 Sepsis HSDN C0013421 Dystonia C0001883 Airway obstruction HSDN C0037316 Not enough sleeping C0020473 Hyperlipidemia HSDN C0026884 Muteness C0001726 Affective symptoms HSDN C4085210 Usual severity pain C0037859 Spermatocele HSDN C2024893 Cardiovascular surgery result: fatigue C0282192 Bolivian hemorrhagic fever MalaCards C0036572 Convulsion C0085426 Gram-positive bacterial infections HSDN C0020438 Hypercalciuria C2609414 Acute kidney injury HSDN C0518090 Frequency of pain question C0870082 Hyperkeratosis HSDN C1279888 Proteinuria of undiagnosed cause C2749685 Cystinosis, atypical nephropathic (disorder) HPO C0231791 In toe C0796037 Martsolf syndrome MalaCards|HPO C0020673 Hypothermia (central) (local) C0022716 Menkes kinky hair syndrome MalaCards|HSDN|HPO C0162834 Hyperpigmentation C1866425 Yemenite deaf-blind hypopigmentation syndrome MalaCards C1963093 Dizziness adverse event C0039980 Chest injury HSDN C0518090 Frequency of pain question C0392622 Toxic effect of carbon tetrachloride HSDN C0085636 Light sensitivity C0152200 Achromatopsia OrphaNet|HPO|MalaCards C0036572 Convulsion C0796070 Microphthalmia, syndromic 7 MalaCards|HPO C0000737 Abdomen pain C2981664 Stage ia distal bile duct cancer UMLS C0042928 Paralysis vocal cord C0033968 Psychotherapeutic technique HSDN C0340288 Angina stable C0011860 Diabetes mellitus, non-insulin-dependent HSDN C2911647 Weight gain adverse event C0242550 Behavior, risk reduction HSDN C0036572 Convulsion C0040100 Thymoma HSDN C4084784 Diarrhea C0025268 Multiple endocrine neoplasia type 2a OrphaNet C4084766 Vomiting C1621920 Intermediate maple syrup urine disease HPO C2984058 Have pain C0042514 Tachycardia, ventricular HSDN C0023015 Language handicap C0033873 Psychiatry HSDN C0015469 Facial paralysis C0009363 Congenital ocular coloboma (disorder) HSDN C2127413 Numbness of outer aspect of both forearms C0457014 Book syndrome MalaCards C0034155 Thrombotic thrombocytopenic purpura C0032285 Pneumonia HSDN C0332563 Papulae C0036220 Kaposi sarcoma OrphaNet C2024893 Cardiovascular surgery result: fatigue C3163843 Chondrosarcoma of bone HSDN C0020672 Body temperature decreased C0019294 Hernia, inguinal HSDN C0917816 Deficiency mental C1439329 Cbs gene HPO C4085222 Nausea C0018916 Hemangioma HSDN C0018772 Deafness C0042138 Uterine neoplasms HSDN C0007758 Cerebellar ataxia C1857662 Coach syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C3553571 Congenital disorder of glycosylation, type iik MalaCards C0518090 Frequency of pain question C0016483 Food preferences HSDN C0015672 Decreased energy C0000809 Abortion, habitual HSDN C3539893 Pelvic pain occurs with intercourse C0033038 Ejaculatio praecox HSDN C0042755 Virilisation C0011581 Depressive disorder HSDN C4084774 Have weight loss C0042995 Vulvar neoplasms HSDN C4084767 Bothered by vomiting C0276357 Swine influenza MalaCards C1963281 Vomiting adverse event C0019202 Hepatolenticular degeneration HSDN C0020438 Hypercalciuria C0013336 Dwarfism HSDN C2012661 Growths on both sclerae C0036412 Sclera UMLS C2936821 Spinal cerebrospinal fluid leak C0010266 Cranial nerve diseases HSDN C4084767 Bothered by vomiting C0030305 Pancreatitis HSDN C0242936 Center pain C0032461 Polycythemia HSDN C1962972 Proteinuria adverse event C0007350 Cat disease HSDN C0751229 Hypersomnolence C0033922 Psychomotor disorders MalaCards C3494358 Characteristic, prodromal C0003873 Rheumatoid arthritis HSDN C3463815 Feel fatigue C0020550 Hyperthyroidism HSDN C0344307 Analgesia C2931828 Keratoderma and spastic paralysis MalaCards C0028738 Nystagmus C1866039 Episodic ataxia, type 5 MalaCards C1963249 Tinnitus adverse event C0001175 Acquired immunodeficiency syndrome HSDN C4084784 Diarrhea C0035412 Rhabdomyosarcoma HSDN C1557397 Adverse event associated with pain C0221002 Hyperparathyroidism, primary HSDN C4084727 Cough frequency C0026764 Multiple myeloma HSDN C0020578 Hyperventilate C0020506 Hyperpituitarism HSDN C0151786 Weakness muscle C0011860 Diabetes mellitus, non-insulin-dependent HSDN C1090821 Sepsis C1832241 Agammaglobulinemia due to early prob cell defect MalaCards|HPO C1963281 Vomiting adverse event C0751285 Maple syrup urine disease, thiamine responsive HPO C0460137 Push down or depress C0032533 Polymyalgia rheumatica MalaCards C1963170 Hypothermia adverse event C0151814 Coronary occlusion HSDN C1963170 Hypothermia adverse event C2004491 Cicatrix HSDN C4084774 Have weight loss C0035243 Respiratory tract infections HSDN C2096293 Ent surgical result ear vertigo C0032209 Platybasia HSDN C0242936 Center pain C0014122 Subacute bacterial endocarditis HSDN C0034150 Skin purpura C0016510 Foot diseases HSDN C1279888 Proteinuria of undiagnosed cause C0271693 Acquired generalized lipodystrophy MalaCards C4084773 Bothered by weight gain C0015579 Family characteristics HSDN C2919142 Short stature adverse event C1856054 Hutterite cerebroosteonephrodysplasia syndrome MalaCards C0033775 Anal pruritus C0810052 Other inflammatory condition of skin UMLS C2029884 Hearing loss by exam C0029401 Osteitis deformans HSDN C4085211 Pain distress question C0037047 Sibling HSDN C1384666 Decreased hearing C0007222 Cardiovascular diseases HSDN C0010520 Skin cyanosis C0006118 Brain neoplasms HSDN C0009398 Color vision defects C0017638 Glioma HSDN C4085210 Usual severity pain C2116082 Finding of thyroid nodule by palpation HSDN C0023222 Lower extremity pain musculoskeletal C0810058 Other connective tissue disease UMLS C4084784 Diarrhea C0030524 Paratuberculosis HSDN C0751295 Memory loss or impairment C0342853 Sialuria OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0334299 Carcinoid tumor no icd-o subtype HSDN C4084727 Cough frequency C0038525 Subarachnoid hemorrhage HSDN C0232462 Appetite decrease C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0020580 Decreased sensation C0399526 Class iii malocclusion HSDN C0522224 Palsied C0342257 Complications of diabetes mellitus HSDN C0023014 Developmental disorder language C0344315 Depressed mood HSDN C0003469 Anxiety disorder C2931859 Acquired cjd MalaCards C0009806 Constipate C0702166 Acne HSDN C0041834 Erythematous condition C0870082 Hyperkeratosis MalaCards C4084776 Weight loss C0270611 Brain damage HSDN C0013362 Dysarthrias C0034345 Pyruvate dehydrogenase complex deficiency disease OrphaNet|MalaCards C0020505 Excessive eating C0017980 Glycosuria, renal MalaCards|HPO C0036572 Convulsion C0027720 Nephrosis HSDN C4084788 Have dizziness C0026266 Mitral valve insufficiency HSDN C4084725 Usual severity cough C0011881 Diabetic nephropathy HSDN C0151686 Growth retardation C2931241 Primary intestinal lymphangiectasis MalaCards C0000737 Abdomen pain C0278699 Childhood hepatoma, group iv UMLS C0013404 Respiratory difficulty C0014848 Esophageal achalasia HSDN C4084784 Diarrhea C3150752 Agammaglobulinemia 4, autosomal recessive HPO C0917816 Deficiency mental C3280799 Cutis laxa, autosomal recessive, type iiib MalaCards C1963091 Diarrhea adverse event C0398689 Hyper-igm immunodeficiency syndrome, type 1 HPO C0013404 Respiratory difficulty C0027666 Neoplasms, radiation-induced HSDN C0039070 Collapse fleeting C1258104 Diffuse scleroderma HSDN C1963091 Diarrhea adverse event C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0036659 Sensation disorder C0007760 Cerebellar diseases HSDN C0002962 Angina C0006114 Cerebral edema HSDN C0030214 Myoclonus palatal C0459146 Disorder of soft tissue of body cavity UMLS C2024878 Cardiovascular surgery result: dyspnea C0013080 Down syndrome HSDN C4084773 Bothered by weight gain C0019569 Hirschsprung disease HSDN C0037317 Sleep disturbance C0023788 Whipple disease OrphaNet|MalaCards C0000727 Abdomen acute C1328520 Abdominal catastrophe UMLS C4084776 Weight loss C0042029 Urinary tract infection HSDN C3274924 Have been coughing C0011616 Contact dermatitis HSDN C0015672 Decreased energy C0236969 Substance-related disorders HSDN C0015469 Facial paralysis C0004610 Bacteremia HSDN C1838869 Proximal neurogenic muscle weakness C1832525 Limb-girdle muscular dystrophy type 2f MalaCards|HPO C1549543 Administration method - pain C0000833 Abscess HSDN C4085661 Usual severity nausea C0032914 Pre-eclampsia HSDN C0010520 Skin cyanosis C0030305 Pancreatitis HSDN C4085210 Usual severity pain C0019348 Herpes simplex infections HSDN C0031911 Pigment deposition C3888065 Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant MalaCards C4085862 Bothered by nausea C0002991 Cutaneous fibrous histiocytoma HSDN C0011570 Monopolar depression C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0019079 Bloody sputum C0242788 Breast neoplasms, male HSDN C2237041 Shox gene with short stature C0220687 Kbg syndrome MalaCards|HPO C4084784 Diarrhea C0001546 Adjustment disorders HSDN C0021359 Infertility C3554453 Spermatogenic failure 11 MalaCards C0917816 Deficiency mental C3695063 Charcot-marie-tooth disease, type 4b3 MalaCards C4084788 Have dizziness C0027947 Neutropenia HSDN C0028738 Nystagmus C0574084 3-methylglutaconic aciduria type 3 OrphaNet|HPO|MalaCards C4084768 Usual severity vomiting C0040336 Tobacco use disorder HSDN C0030552 Paralysis partial C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards C1263846 Attention deficit disorder with hyperactivity C0265286 Dyggve-melchior-clausen syndrome MalaCards|HPO C3463815 Feel fatigue C0009400 Colorado tick fever DiseaseOntology|MalaCards C0012833 Dizzy C0037952 Spinocerebellar degeneration HSDN C0042963 Symptoms vomiting C0011269 Dementia, vascular HSDN C0009421 Comatose C0029443 Osteomyelitis HSDN C0042024 Urine incontinence C0021368 Inflammation HSDN C0860603 Anxiety symptom C2932715 Pseudohypoparathyroidism type 1b MalaCards|HPO C2919142 Short stature adverse event C0473586 Michelin tire baby syndrome MalaCards|HPO C3898969 Have been vomiting C0079731 B-cell lymphomas HSDN C0042963 Symptoms vomiting C0038463 Strongyloides infection HSDN C0015672 Decreased energy C0005695 Bladder neoplasm HSDN C1549543 Administration method - pain C0242188 Spider bites HSDN C0015468 Face pain C0016064 Fibrous dysplasia, monostotic HSDN C2032395 Pelvic pain on the left C0034888 Rectal prolapse HSDN C0575081 Abnormal gait C0028064 Niemann-pick diseases MalaCards C1963087 Constipation adverse event C0079294 Epidermolysis bullosa dystrophica OrphaNet C0013604 Edematous C0035328 Retinal vein occlusion HSDN C0000737 Abdomen pain C0040715 Chromosomal translocation HSDN C0010200 Cough symptom C1552262 Nurse practitioner - family HSDN C0727671 Red cross toothache drops C0997768 Glaucoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0206733 Strawberry nevus of skin HSDN C0700590 Diaphoresis excessive C1835663 Keratosis palmaris et plantaris with clinodactyly OrphaNet|MalaCards C4084766 Vomiting C0338480 Common migraine HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0010273 Craniofacial dysostosis HSDN C0030794 Pelvis pain C0015558 Fallopian tube neoplasms HSDN C4084724 Usual severity constipation C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0518090 Frequency of pain question C0022667 Papillary necrosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032460 Polycystic ovary syndrome HSDN C3463815 Feel fatigue C0344434 Atrial fibrillation ecg HSDN C4084725 Usual severity cough C0032966 Complication, neoplastic pregnancy HSDN C0002622 Amnesias C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0030193 Sense of pain C0030470 Paranasal sinus neoplasms HSDN C0030975 Disorders perception C0026848 Myopathy HSDN C1963091 Diarrhea adverse event C0398788 Immunodeficiency syndrome, variable MalaCards|HPO C1999266 Depression adverse event C2936346 22q11 deletion syndrome MalaCards C0406402 Erythema fugax C0037274 Dermatologic disorders UMLS C0013604 Edematous C0030489 Paraproteinemias HSDN C4084784 Diarrhea C0039231 Tachycardia HSDN C3539889 Pelvic pain increasing in severity C0269185 Uterus retroverted HSDN C3641756 Have diarrhea C0008325 Cholecystitis HSDN C0036396 Sciatica C0553730 Calcium pyrophosphate deposition disease HSDN C0497406 Over weight C0025521 Inborn errors of metabolism HSDN C0042963 Symptoms vomiting C0017128 Fistula gastric HSDN C0020615 Hypoglycemia nos C0016751 Hereditary fructose intolerance syndrome HPO C4085210 Usual severity pain C0221752 Rbc urine HSDN C0018772 Deafness C1720864 Sulfatidosis, juvenile, austin type MalaCards|HPO C1384666 Decreased hearing C0043168 Whooping cough due to unspecified organism HSDN C0263571 Chloasma gravidarum C0151864 Disorder of pregnancy UMLS C3665347 Vision impaired C1844776 Cone-rod dystrophy, x-linked, 1 MalaCards|HPO C1963184 Nystagmus adverse event C1855565 Pyruvate dehydrogenase e2 deficiency MalaCards|HPO C0019825 Voice hoarseness C0153653 Malignant tumor of parathyroid gland MalaCards C0026821 Cramp C0018800 Cardiomegaly HSDN C0424755 Fever symptoms C0878675 Erdheim-chester disease OrphaNet|MalaCards C0038990 Sweats C1868633 Paragangliomas with sensorineural hearing loss HPO C0232466 Feeding difficulty C3810023 Verheij syndrome MalaCards C4084773 Bothered by weight gain C0020619 Hypogonadism HSDN C0085631 Abnormal excitement C0085102 Chromotherapy HSDN C1961131 Cough adverse event C0023448 Lymphoid leukemia HSDN C1963071 Back pain adverse event C0029118 Opportunistic infections HSDN C0151908 Dry skin C2940786 Thyroid hormone resistance syndrome HPO C2984058 Have pain C0013363 Dysautonomia HSDN C0018991 Paralysis one side of body C0030508 Parasomnia HSDN C0004134 Dyssynergia C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HSDN C4085210 Usual severity pain C0010417 Cryptorchidism HSDN C0162835 Hypopigmentation C0268374 Adult junctional epidermolysis bullosa (disorder) OrphaNet|MalaCards C4085548 Usual severity dizziness C0027663 Neoplasms, multiple primary HSDN C1963091 Diarrhea adverse event C0717360 Disease lyme vaccine HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0037933 Spinal diseases HSDN C0029163 Hemorrhage mouth C1837218 Cleft palate, isolated HSDN C0027796 Neuralgias C0027092 Myopia HSDN C0026838 Spasticity muscle C1845366 Mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance MalaCards|HPO|UMLS C0036572 Convulsion C1857277 Donnai-barrow syndrome MalaCards|HPO C0042963 Symptoms vomiting C0017668 Focal glomerulosclerosis HSDN C2132198 Abnormal blistering of the skin C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C0151594 Bloody diarrhea C2674051 Inflammatory bowel disease 11 MalaCards C0150055 Pain chronic C0019080 Hemorrhage HSDN C0040259 Tinea pedis C0007222 Cardiovascular diseases HSDN C1963091 Diarrhea adverse event C0022408 Arthropathy HSDN C0349588 Stature short C1868508 Kosenow syndrome MalaCards C3829611 Nausea frequency C0042075 Urologic diseases HSDN C2188005 Fainting with unconsciousness lasting for 15 seconds or less C0234431 Brief loss of consciousness UMLS C0035078 Failure kidney C0085548 Autosomal recessive polycystic kidney disease OrphaNet|HPO C0241210 Speaking delay C1968552 Mental retardation, x-linked, with spasticity HPO C4084725 Usual severity cough C0007137 Squamous cell carcinoma HSDN C0018777 Deafness, conductive C0796133 Ramon syndrome MalaCards C3827868 Tachycardia by ecg finding C0013364 Dysautonomia, familial HPO C1963091 Diarrhea adverse event C1704212 Embolism embolus HSDN C3641756 Have diarrhea C0013080 Down syndrome HSDN C0012833 Dizzy C0023343 Leprosy HSDN C0013428 Painful urination C0030793 Pelvis tumor HSDN C0040485 Wryneck C0024141 Lupus erythematosus, systemic HSDN C0231528 Muscle pain generalized C0268342 Ehlers-danlos syndrome type 6 MalaCards C0857305 Thrombocytopenia purpura C0041316 Lymph node tuberculosis HSDN C2024893 Cardiovascular surgery result: fatigue C0027809 Neurilemmoma HSDN C0332563 Papulae C1836522 Schindler disease, type ii OrphaNet|HPO C1962972 Proteinuria adverse event C0019202 Hepatolenticular degeneration MalaCards|HPO C1963071 Back pain adverse event C0023290 Leishmaniasis, visceral HSDN C0857305 Thrombocytopenia purpura C1258104 Diffuse scleroderma HSDN C0026838 Spasticity muscle C0005424 Biliary tract diseases HSDN C4085862 Bothered by nausea C0085083 Ovarian hyperstimulation syndrome OrphaNet|HPO|MalaCards C0001825 Agraphia C0007786 Brain ischemia HSDN C0036659 Sensation disorder C0026847 Spinal muscular atrophy HSDN C0030552 Paralysis partial C0007131 Non-small cell lung carcinoma HSDN C0085631 Abnormal excitement C0497327 Dementia UMLS C0013362 Dysarthrias C1862441 Ataxia, spastic, with congenital miosis OrphaNet|MalaCards C3665492 Pigmentations C0153414 Malignant neoplasm of middle third of esophagus MalaCards C0020580 Decreased sensation C0206734 Hemangioblastoma HSDN C2700617 Irritation - emotion C2678416 Hyperphenylalaninemia, non-pku mild HPO C0026838 Spasticity muscle C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0270948 Neurogenic muscular atrophy C0020072 Hereditary sensory autonomic neuropathy, type 2 OrphaNet|HPO C0018772 Deafness C0017658 Glomerulonephritis HSDN C1963170 Hypothermia adverse event C0020541 Hypertension, portal HSDN C0727671 Red cross toothache drops C0037274 Dermatologic disorders HSDN C4085211 Pain distress question C0000821 Threatened abortion HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0004589 B. anthracis HSDN C3714772 Fever recurrent C2316212 Cryopyrin-associated periodic syndromes MalaCards C0237326 Defecation pain C0270726 Alexander disease OrphaNet|MalaCards C0270948 Neurogenic muscular atrophy C3810001 Combined oxidative phosphorylation deficiency 18 MalaCards C4085862 Bothered by nausea C0023798 Lipoma HSDN C4085211 Pain distress question C1691215 Penile hypospadias HSDN C0022346 Yellow skin C1859722 Arthrogryposis renal dysfunction cholestasis syndrome MalaCards|HPO|UMLS C2203646 Jaundice C0014848 Esophageal achalasia HSDN C1962972 Proteinuria adverse event C0021070 Immunoproliferative disease HSDN C0012833 Dizzy C0023092 Lassa fever OrphaNet|MalaCards C2911645 Weight loss adverse event C0017185 Gastrointestinal neoplasms HSDN C2029884 Hearing loss by exam C0011854 Diabetes mellitus, insulin-dependent HSDN C0009792 Consciousness disorder C0270612 Leukoencephalopathies HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035412 Rhabdomyosarcoma HSDN C0270948 Neurogenic muscular atrophy C0398791 Nijmegen breakage syndrome MalaCards|HPO C3146279 Coma C0009375 Colonic neoplasms HSDN C0038990 Sweats C0022283 Incontinentia pigmenti achromians OrphaNet|HPO|MalaCards C0027497 Queasy C0027663 Neoplasms, multiple primary HSDN C2911645 Weight loss adverse event C1868594 Perry syndrome OrphaNet|HPO|MalaCards C0243026 Generalized infection C0079218 Fibromatosis, aggressive MalaCards|HPO C0005745 Blepharoptosis C2673677 Myopathy, early-onset, with fatal cardiomyopathy MalaCards|HPO C0018991 Paralysis one side of body C0035220 Respiratory distress syndrome, newborn HSDN C0013456 Pain ear C0008441 Chondroblastoma HSDN C2315100 Pediatric failure to thrive C0162671 Melas syndrome HSDN C0332573 Macula C0027831 Neurofibromatosis 1 OrphaNet C1549543 Administration method - pain C0017400 Behavioral genetics HSDN C3463815 Feel fatigue C1136033 Cutaneous mastocytosis MalaCards C0003467 Angst C1859252 Cerebrofaciothoracic dysplasia MalaCards C1963184 Nystagmus adverse event C1850442 Ceroid lipofuscinosis, neuronal, 5 MalaCards|HPO C0751837 Gait ataxic C1832585 Cerebellar ataxia, cayman type HPO C0086565 Liver function abnormal C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0042798 Vision dim C0030297 Pancreatic neoplasm HSDN C0344435 Ventricular fibrillation by ecg finding C3501851 Long qt syndrome 2-5 MalaCards C0020673 Hypothermia (central) (local) C0342257 Complications of diabetes mellitus HSDN C4085317 Diarrhea frequency C1253943 Fluid in the chest HSDN C3665347 Vision impaired C3554079 Combined oxidative phosphorylation deficiency 12 MalaCards C4084773 Bothered by weight gain C0600260 Lung diseases, obstructive HSDN C2936821 Spinal cerebrospinal fluid leak C0333596 Deposition of iron HSDN C2024878 Cardiovascular surgery result: dyspnea C0034040 Puerperal disorders HSDN C0020672 Body temperature decreased C0016057 Fibrosarcoma HSDN C4084768 Usual severity vomiting C0342788 Renal carnitine transport defect OrphaNet|HPO|MalaCards C2875626 Eyelid retraction right eye, unspecified eyelid C0497217 Other disease of eye UMLS C0002962 Angina C0040137 Thyroid nodule HSDN C0018681 Headache, cephalalgia C1367460 Lats1 gene HSDN C1557397 Adverse event associated with pain C0017154 Gastritis, atrophic HSDN C0857305 Thrombocytopenia purpura C0236969 Substance-related disorders HSDN C4042891 Sleep wake disorders C0038395 Streptococcal infections HSDN C0085636 Light sensitivity C2751316 Glaucoma 3, primary congenital, d MalaCards|HPO C0024032 Birth weight subnormal C3810012 Rienhoff syndrome MalaCards C2984058 Have pain C0206180 Ki-1+ anaplastic large cell lymphoma HSDN C0042798 Vision dim C0339510 Vitelliform macular dystrophy OrphaNet|HPO|MalaCards C3641756 Have diarrhea C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C1963063 Anorexia adverse event C0021799 Interprofessional relations HSDN C1963087 Constipation adverse event C0030297 Pancreatic neoplasm HSDN C4085642 Level of joint stiffness C0043119 Werner syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0042029 Urinary tract infection HSDN C0010200 Cough symptom C1266034 Bronchiolo-alveolar carcinoma, non-mucinous UMLS C4084766 Vomiting C0014335 Enteritis HSDN C3665346 Loss sight C0017609 Glaucoma, neovascular OrphaNet|MalaCards C0000737 Abdomen pain C3714605 Of pain perception HSDN C4085211 Pain distress question C0004775 Bartter disease HSDN C0005745 Blepharoptosis C2675066 Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus HPO C0019825 Voice hoarseness C0265514 Dermatofibrosis lenticularis disseminata MalaCards|HPO C4020887 Photodysphoria C1846529 Cone-rod dystrophy 10 MalaCards|HPO C0375224 Monoplegia of lower limb affecting unspecified side C0085622 Monoplegia unspecified UMLS C0020673 Hypothermia (central) (local) C0022650 Kidney calculi HSDN C0015469 Facial paralysis C0432269 Lenz majewski hyperostotic dwarfism MalaCards C0241210 Speaking delay C3279738 Cerebral palsy, spastic quadriplegic, 5, formerly MalaCards C0011991 Loose stools C0031046 Pericarditis HSDN C1384666 Decreased hearing C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards C4084769 Vomiting frequency C3163620 Hypotension adverse event HSDN C4085211 Pain distress question C2219717 Menstrual periods stopped for over 6 months HSDN C4084767 Bothered by vomiting C0556346 Binge drinking HSDN C0037317 Sleep disturbance C3160718 Parkinson disease, late-onset MalaCards|HPO|UMLS C0018784 Deafness sensorineural C1864852 Catshl syndrome HPO C0013604 Edematous C0085273 Erythema infectiosum HSDN C4049644 Depression C0566602 Primary sclerosing cholangitis MalaCards|HPO C0013395 Indigestion C0034065 Pulmonary embolism HSDN C1963137 Hydrocephalus adverse event C0432443 Deletion of long arm of chromosome 18 MalaCards C0085636 Light sensitivity C0302129 Achromatopsia 1 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0018922 Hemangiopericytoma HSDN C0917816 Deficiency mental C2936863 Bardet-biedl syndrome 2 (disorder) MalaCards C4085210 Usual severity pain C0018199 Granuloma, plasma cell HSDN C1279888 Proteinuria of undiagnosed cause C0024305 Lymphoma, non-hodgkin HSDN C0851578 Disorder sleep C1837218 Cleft palate, isolated HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C4042784 Feeding and eating disorders HSDN C0242936 Center pain C0162836 Hidradenitis suppurativa HSDN C0013390 Cramps menstrual C0003850 Arteriosclerosis HSDN C0020538 Hbp C1859727 Arterial calcification of infancy MalaCards|HPO C2362324 Pediatric obesity C1257763 Overnutrition HSDN C0036572 Convulsion C0234547 Convulsions drug withdrawal UMLS C0522224 Palsied C0037274 Dermatologic disorders HSDN C0039070 Collapse fleeting C0040046 Thrombophlebitis HSDN C0020450 Hyperemesis gravidarum C0034183 Pyelitis unspecified HSDN C0576456 Poor feeding C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C0454644 Delayed language development C1510586 Autism spectrum disorders HPO C0042963 Symptoms vomiting C0040558 Toxoplasmosis HSDN C4084724 Usual severity constipation C0019372 Herpesviridae infections HSDN C0007758 Cerebellar ataxia C0033860 Psoriasis HSDN C0030193 Sense of pain C1519912 Vaginal adenoid cystic carcinoma UMLS C0009421 Comatose C0085437 Meningitis, bacterial HSDN C0026838 Spasticity muscle C1881674 Medical device emits smoke HSDN C0751352 Myoclonus nocturnal C0030508 Parasomnia UMLS C0000737 Abdomen pain C0751674 Lymphangioleiomyomatosis OrphaNet|HSDN|HPO|MalaCards C2017374 Right leg soft tissue swelling with bluish discoloration C0037580 Soft tissue swelling UMLS C1963184 Nystagmus adverse event C0432262 Dysosteosclerosis OrphaNet|HPO|MalaCards C0003862 Pain joint C1720777 Functional laterality HSDN C0037316 Not enough sleeping C0006118 Brain neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0270948 Neurogenic muscular atrophy C1854663 Chudley rozdilsky syndrome OrphaNet|MalaCards C0030794 Pelvis pain C0009240 Cognition HSDN C4084724 Usual severity constipation C0042812 Acuity visual HSDN C0031154 Peritonitis, nos C1334818 Multicystic mesothelioma of peritoneum MalaCards C0151786 Weakness muscle C0270611 Brain damage HSDN C4085210 Usual severity pain C0035220 Respiratory distress syndrome, newborn HSDN C0005745 Blepharoptosis C1847874 Phace association MalaCards C0011991 Loose stools C0019294 Hernia, inguinal HSDN C1549543 Administration method - pain C0348018 Projections HSDN C0518090 Frequency of pain question C3658267 Prostatic neoplasms, castration-resistant HSDN C2096293 Ent surgical result ear vertigo C0020649 Hypotension HSDN C0851578 Disorder sleep C1868570 Char syndrome MalaCards C3274924 Have been coughing C0032965 Pregnancy complications, infectious HSDN C0036572 Convulsion C0262655 Recurrent urinary tract infection HSDN C4085211 Pain distress question C0162557 Liver failure, acute HSDN C0085593 Chill C0024535 Malaria, falciparum HSDN C0041657 Consciousness loss C0001430 Adenoma HSDN C2984058 Have pain C0022595 Keratosis follicularis HSDN C1557397 Adverse event associated with pain C0702166 Acne HSDN C0271215 Blindness legal C0432252 Osteoporosis with pseudoglioma MalaCards|HPO C0030794 Pelvis pain C1519923 Gartner duct adenocarcinoma UMLS C2024878 Cardiovascular surgery result: dyspnea C0009404 Colorectal neoplasms HSDN C0037316 Not enough sleeping C0001807 Aggressive behavior HSDN C0020649 Blood pressure decreased C0854176 Malignant hepato-biliary neoplasm MalaCards C0042571 Vertigo subjective C0005586 Bipolar disorder HSDN C2984058 Have pain C0018571 Hand injury HSDN C0012569 Double vision C0015414 Eye neoplasms HSDN C0030193 Sense of pain C0011606 Exfoliative dermatitis HSDN C0040034 Thrombocytopenia C0279607 Adult primary hepatocellular carcinoma MalaCards C0030193 Sense of pain C1707042 Breast carcinoma with cartilaginous metaplasia UMLS C0030193 Sense of pain C0014550 Epilepsies, myoclonic HSDN C0242936 Center pain C0040441 Broken teeth HSDN C4085211 Pain distress question C0039373 Tay-sachs disease HSDN C2984058 Have pain C0002940 Aneurysm HSDN C0007859 Pain neck C0040136 Thyroid neoplasm HSDN C0043352 Absent salivary secretion C0014805 Primary erythermalgia MalaCards|HPO C0002962 Angina C0007786 Brain ischemia HSDN C0035078 Failure kidney C0151467 Addisonian crisis OrphaNet|MalaCards C0030193 Sense of pain C0242188 Spider bites HSDN C1963091 Diarrhea adverse event C1145628 Autonomic nervous system disorders HSDN C0518090 Frequency of pain question C0027121 Myositis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0206369 Splenosis HSDN C0003469 Anxiety disorder C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0038506 Stutter C0028768 Obsessive-compulsive disorder HSDN C0026838 Spasticity muscle C3553529 Combined oxidative phosphorylation deficiency 10 MalaCards C0023014 Developmental disorder language C0038263 Stereognoses HSDN C1963093 Dizziness adverse event C0005695 Bladder neoplasm HSDN C0040034 Thrombocytopenia C1856465 Ghosal hematodiaphyseal dysplasia HPO C3641756 Have diarrhea C3665596 Warts HSDN C0018991 Paralysis one side of body C0014557 Epilepsy, post-traumatic HSDN C0030193 Sense of pain C0005119 Bereavement HSDN C1384666 Decreased hearing C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C4084724 Usual severity constipation C0014805 Primary erythermalgia MalaCards|HPO C0026838 Spasticity muscle C0751664 Canavan disease, neonatal OrphaNet|HPO C4084768 Usual severity vomiting C0040136 Thyroid neoplasm HSDN C2029884 Hearing loss by exam C0010273 Craniofacial dysostosis HSDN C3274924 Have been coughing C1258090 Enzootic pneumonia of pigs HSDN C0027497 Queasy C0001418 Adenocarcinoma HSDN C4085210 Usual severity pain C0206654 Leiomyomatosis HSDN C0018834 Brash C0220730 Fryns syndrome MalaCards|HPO C3898969 Have been vomiting C0024523 Malabsorption syndrome MalaCards|HSDN C0000737 Abdomen pain C0518450 Spinal fractures HSDN C1963087 Constipation adverse event C1290375 Mesothelioma (malignant, clinical disorder) (disorder) HSDN C0002963 Angina variant C3812171 Bradycardia by ecg finding HSDN C4084775 Usual severity weight loss C0027439 Nasopharyngeal neoplasms HSDN C1557397 Adverse event associated with pain C1963164 Lymphopenia adverse event HSDN C0013421 Dystonia C0020458 Hyperhidrosis disorder HSDN C0009806 Constipate C0279643 Undifferentiated carcinoma of colon UMLS C0004604 Pain back C0017178 Gastrointestinal diseases HSDN C1963252 Tremor adverse event C0006840 Candidiasis HSDN C0042963 Symptoms vomiting C0026857 Musculoskeletal diseases HSDN C0518090 Frequency of pain question C0025292 Haemophilus meningitis HSDN C0014534 Epididymitis unspecified C0013884 Filarial elephantiases DiseaseOntology C0795692 Lactate blood increased C0020621 Hypokalemia HSDN C0007398 Catatonic C0043251 Wounds and injuries HSDN C2939013 Troisier's sign C0686619 Secondary malignant neoplasm of lymph node UMLS C0033377 Caudal displacement C1854663 Chudley rozdilsky syndrome OrphaNet|MalaCards C0023014 Developmental disorder language C0026118 Situational therapy HSDN C3815497 Cough C0001580 Adolescent behavior HSDN C3641755 Have constipation C0034067 Pulmonary emphysema HSDN C0032285 Pneum C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C2024893 Cardiovascular surgery result: fatigue C0022350 Jaundice, chronic idiopathic MalaCards|HPO C1691779 Hearing disorder, cochlear C2931258 Amaurosis congenita of leber, type 1 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0042826 Field visual HSDN C1384666 Decreased hearing C1136043 Acoustic schwannoma, bilateral HPO C0184567 Pain acute C0043251 Wounds and injuries HSDN C0751837 Gait ataxic C0008066 Child behavior disorders HSDN C0241137 Skin pallor C2750063 Leber congenital amaurosis 14 MalaCards|HPO C3665492 Pigmentations C0155160 Conjunctival degeneration unsp MalaCards C2024893 Cardiovascular surgery result: fatigue C0040820 Trematode infections HSDN C1963067 Atrial fibrillation adverse event C2678477 Brugada syndrome 4 MalaCards|HPO C1963281 Vomiting adverse event C0016169 Pathologic fistula HSDN C0020673 Hypothermia (central) (local) C4084909 Depression subordinate domain HSDN C0015469 Facial paralysis C0023895 Liver diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0034088 Pulmonary valve insufficiency HSDN C1963252 Tremor adverse event C0009450 Disease caused by microorganism HSDN C0020538 Hbp C1859568 Bardet-biedl syndrome 10 HPO C0036396 Sciatica C0011853 Diabetes mellitus, experimental HSDN C2315100 Pediatric failure to thrive C0024312 Lymphopenia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007130 Mucinous adenocarcinoma HSDN C0349588 Stature short C0004135 Ataxia telangiectasia OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0023518 Leukocytosis HSDN C4084788 Have dizziness C0002989 Epithelioid hemangioma of skin HSDN C0917816 Deficiency mental C4014435 Mental retardation, autosomal dominant 26 MalaCards C0033774 Skin pruritus C0022665 Kidney neoplasm HSDN C0007758 Cerebellar ataxia C0009207 Cockayne syndrome OrphaNet|MalaCards C0221232 Welts C0343068 Familial cold urticaria UMLS C0030552 Paralysis partial C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C0242936 Center pain C0028850 Ocular motility disorders HSDN C0002962 Angina C0018814 Heart rupture, post-infarction HSDN C1557397 Adverse event associated with pain C0039106 Pigmented villonodular synovitis HSDN C2024893 Cardiovascular surgery result: fatigue C0027902 Neuropsychological diagnosis HSDN C0221232 Welts C0263340 Urticaria pigmentosa, infantile form UMLS C0013362 Dysarthrias C1853247 Spastic paraplegia 31, autosomal dominant MalaCards|HPO C0860603 Anxiety symptom C2936346 22q11 deletion syndrome MalaCards|HPO C3665347 Vision impaired C2931241 Primary intestinal lymphangiectasis MalaCards C0428977 Pulse rate decrease C4015474 Chronic atrial and intestinal dysrhythmia MalaCards C0424755 Fever symptoms C0023269 Leiomyosarcoma HSDN C0018681 Headache, cephalalgia C0002892 Anemia, pernicious HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0023788 Whipple disease MalaCards C0018777 Deafness, conductive C1842870 Chromosome 1p36 deletion syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0021361 Female infertility HSDN C4084775 Usual severity weight loss C0032927 Precancerous conditions HSDN C0042571 Vertigo subjective C0000833 Abscess HSDN C0557874 Global developmental delay C3553597 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome MalaCards C0033377 Caudal displacement C2931557 Chromosome 4 short arm deletion MalaCards C0009806 Constipate C0017181 Gastrointestinal hemorrhage HSDN C4084768 Usual severity vomiting C0007134 Renal cell carcinoma HSDN C0278152 Hemifacial spasms C0004936 Mental disorders HSDN C0018926 Emesis bloody C0001175 Acquired immunodeficiency syndrome HSDN C0018772 Deafness C0019054 Hemolysis (disorder) HSDN C3887638 Failure to thrive in infant C0553578 Non-bullous ichthyosiform erythroderma MalaCards C4085210 Usual severity pain C0014856 Esophageal fistula HSDN C0522224 Palsied C0036421 Systemic scleroderma HSDN C3898969 Have been vomiting C1847839 Episodic ataxia, type 3 MalaCards C4084723 Constipation C2984291 Glioblastoma multiforme pathway HSDN C1963063 Anorexia adverse event C0043397 Yellow fever, jungle MalaCards C0007398 Catatonic C0028768 Obsessive-compulsive disorder HSDN C4084767 Bothered by vomiting C0026780 Mumps HSDN C0018524 Hallucinate C0751279 Metachromatic leukodystrophy, adult-type (disorder) HPO C0020578 Hyperventilate C0037929 Spinal cord injuries HSDN C0857305 Thrombocytopenia purpura C1858664 Hemochromatosis, type 3 MalaCards C0277959 Hair coarseness C0026706 Mucopolysaccharidosis iii OrphaNet|MalaCards C2984058 Have pain C0013533 Echovirus infections HSDN C0015469 Facial paralysis C0037369 Smoking HSDN C1963093 Dizziness adverse event C0271375 Cranial nerve palsy iv trochlear HSDN C0033377 Caudal displacement C3550903 Cornelia de lange syndrome 5 MalaCards C2187990 Unable to perform sex C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C3146279 Coma C1856143 Hemolytic uremic syndrome, typical MalaCards C2315100 Pediatric failure to thrive C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C2203646 Jaundice C0008924 Cleft lip HSDN C0242936 Center pain C0085083 Ovarian hyperstimulation syndrome HSDN C0004310 Auditory disorder process C0001175 Acquired immunodeficiency syndrome HSDN C0022107 Fussiness C3887678 Cpnet MalaCards C1963063 Anorexia adverse event C0018790 Cardiac arrest HSDN C0011991 Loose stools C0267660 Chronic diarrhea of infants and young children UMLS C0015469 Facial paralysis C0007361 Cat-scratch disease HSDN C0233794 Memory impaired C1843792 Frontotemporal lobar degeneration with tdp43 inclusions, grn-related HPO C0027066 Myoclonic jerking C2931846 Myoclonic epilepsy with choreoathetosis HPO C4084766 Vomiting C0019270 Hernia HSDN C4085862 Bothered by nausea C0009319 Colitis HSDN C0004134 Dyssynergia C0919524 Atm gene HPO C0027497 Queasy C1552262 Nurse practitioner - family HSDN C0557874 Global developmental delay C1833102 Diabetes mellitus, permanent neonatal, with neurologic features HPO C0027497 Queasy C1962986 Glaucoma adverse event HSDN C0518090 Frequency of pain question C0017412 Genital diseases, male HSDN C4085317 Diarrhea frequency C0002171 Alopecia areata HSDN C3274924 Have been coughing C0205788 Histiocytoid hemangioma HSDN C0015938 Fetal macrosomia C1963138 Hypertension adverse event HSDN C2919142 Short stature adverse event C0162809 Kallmann syndrome OrphaNet|HPO C0237326 Defecation pain C1275808 Congenital central hypoventilation MalaCards|HPO C0454644 Delayed language development C0796225 Mental retardation, x-linked 19 HPO C2242996 Tingling C0025299 Meningocele HSDN C0424755 Fever symptoms C0042171 Uveoparotid fever HSDN C0221263 Cafe au lait spot C0009730 Spinal meningocele HSDN C0013604 Edematous C0005830 Blood protein disorders HSDN C4084802 Usual severity diarrhea C0027932 Neurotic disorders HSDN C4085211 Pain distress question C0022729 Klebsiella infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0015732 Fecal incontinence HSDN C2911645 Weight loss adverse event C0026936 Mycoplasma infections HSDN C0004604 Pain back C0027666 Neoplasms, radiation-induced HSDN C0041105 Jaw spasm C0029443 Osteomyelitis HSDN C0085631 Abnormal excitement C0001969 Alcoholic intoxication HSDN C0039870 Leanness C0024299 Lymphoma HSDN C0232466 Feeding difficulty C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards C0042940 Disorder of voice C0014544 Epilepsy HSDN C1384666 Decreased hearing C1843232 Deafness, autosomal dominant 52 MalaCards C1549543 Administration method - pain C0020437 Hypercalcemia HSDN C0018777 Deafness, conductive C0917715 Hajdu-cheney syndrome MalaCards|HPO C1549543 Administration method - pain C1306577 Dies patient HSDN C2984058 Have pain C0022373 Disease, jejunal HSDN C0042420 Vasovagal episode C3810814 Myocardial infarction ecg assessment HSDN C0018772 Deafness C1848816 Thumb, hypoplastic, with choroid coloboma, poorly developed antihelix, and deafness OrphaNet|MalaCards C4085222 Nausea C0003486 Aortic aneurysm HSDN C0009460 Communication impairment C0005491 Biofeedback HSDN C0028738 Nystagmus C1857252 2,4-dienoyl-coa reductase deficiency MalaCards C0427055 Face weakness C0221060 Mobius syndrome OrphaNet|HPO|MalaCards C0019209 Large liver C0004576 Babesiosis OrphaNet|MalaCards C0030552 Paralysis partial C1959582 Pten hamartoma tumor syndrome MalaCards C1962957 Flushing adverse event C0023896 Alcoholic liver diseases HSDN C0030193 Sense of pain C0151740 Intracranial hypertension HSDN C0018784 Deafness sensorineural C0007786 Brain ischemia HSDN C1549543 Administration method - pain C0043324 Juvenile xanthogranuloma HSDN C0011991 Loose stools C0034530 Injury radiation HSDN C1963091 Diarrhea adverse event C1254288 Anthrax HSDN C0026821 Cramp C0919267 Ovarian neoplasm HSDN C0036572 Convulsion C0007138 Carcinoma, transitional cell HSDN C0039070 Collapse fleeting C1704972 Genomic orientation HSDN C1963180 Neck pain adverse event C0027643 Neoplasm recurrence, local HSDN C0034933 Abnormal reflexes C0004936 Mental disorders HSDN C4042891 Sleep wake disorders C0023066 Laryngismus HSDN C0235153 Sensory hallucination C0027404 Narcolepsy OrphaNet|HPO|MalaCards C0240715 Perineal lump C1290429 Neoplasm of blood vessel of perineum UMLS C0237326 Defecation pain C0268579 Propionic acidemia OrphaNet|HPO C0030193 Sense of pain C0002884 Hypochromic anemia HSDN C0460137 Push down or depress C1956390 Cranial arteritis MalaCards C1557397 Adverse event associated with pain C0035923 German measles vaccine HSDN C0042963 Symptoms vomiting C0038587 Substance withdrawal syndrome HSDN C4085317 Diarrhea frequency C0020295 Hydronephrosis HSDN C0020580 Decreased sensation C0003892 Neurogenic arthropathy HSDN C4084774 Have weight loss C2931038 Pancreatic carcinoma, familial MalaCards C2984058 Have pain C0001314 Acute disease HSDN C0030193 Sense of pain C0015959 Fetomaternal bleeding HSDN C0010200 Cough symptom C1962958 Hematoma adverse event HSDN C0032617 High urine output C0033805 Pseudohypoaldosteronism HSDN C1961131 Cough adverse event C0014544 Epilepsy HSDN C3815497 Cough C1848814 Thymoma, familial MalaCards C4085661 Usual severity nausea C0043253 Trauma blunt HSDN C0518090 Frequency of pain question C2936350 Plaque, atherosclerotic HSDN C3829611 Nausea frequency C0013292 Obstruction duodenal HSDN C4085549 Dizziness C0021603 Sleep initiation and maintenance disorders HSDN C0009460 Communication impairment C0011854 Diabetes mellitus, insulin-dependent HSDN C0398650 Idiopathic thrombocytopenia purpura C1546847 Entity name part type - family HSDN C0017181 Gastrointestinal bleed C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0020538 Hbp C0342749 Glycogen storage disease ic MalaCards|HPO C4084724 Usual severity constipation C0008625 Chromosome aberrations HSDN C0004093 Asthenia C0497327 Dementia HSDN C4085211 Pain distress question C0013808 Electroconvulsive therapy HSDN C0344315 Mood depressed C0878682 Ceruloplasmin deficiency OrphaNet|HPO|MalaCards C0013428 Painful urination C0009774 Conjunctivitis viral HSDN C1963281 Vomiting adverse event C0020541 Hypertension, portal HSDN C0018965 Blood urine C2931253 Alport syndrome, dominant type MalaCards C0454644 Delayed language development C1838570 Ceroid lipofuscinosis, neuronal, 8 MalaCards|HPO C0151686 Growth retardation C3808988 Fanconi anemia, complementation group q MalaCards C4084727 Cough frequency C0033975 Psychotic disorders HSDN C0023015 Language handicap C1963138 Hypertension adverse event HSDN C0018775 Hearing loss bilateral C4084909 Depression subordinate domain HSDN C0033377 Caudal displacement C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C2242577 Oromandibular dystonia C1414216 Dystonia 6, torsion (disorder) MalaCards|HPO C0020673 Hypothermia (central) (local) C1527298 Dysentery, bacillary HSDN C0018524 Hallucinate C0238265 Encephalopathy, callosal demyelinating HSDN C0043094 Weight gain C0344479 Spinal cord myelodysplasia HSDN C1963137 Hydrocephalus adverse event C0220686 Aase smith syndrome MalaCards C0003811 Cardiac rhythm disturbance C1862169 Brachydactyly, long-thumb type MalaCards C1963184 Nystagmus adverse event C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C3641755 Have constipation C0027662 Multiple endocrine neoplasia HSDN C0851578 Disorder sleep C0236964 Attention deficit and disruptive behavior disorders HSDN C3887638 Failure to thrive in infant C2931242 Familial waldmann's disease MalaCards C4084723 Constipation C0030286 Pancreatic diseases HSDN C0043094 Weight gain C0037579 Soft tissue neoplasms HSDN C0042024 Urine incontinence C0751278 Metachromatic leukodystrophy, infant MalaCards|HPO C4084727 Cough frequency C1956391 Temporal arteritis MalaCards|HPO C4084769 Vomiting frequency C0556520 Psychological desensitization HSDN C0013390 Cramps menstrual C0009374 Colonic disease, functional HSDN C0018780 Frequencies hearing high loss C3495801 Granulomatosis with polyangiitis HSDN C0851578 Disorder sleep C0004275 Attitude health HSDN C1963071 Back pain adverse event C2984291 Glioblastoma multiforme pathway HSDN C0018772 Deafness C0086626 Minamata disease OrphaNet C4085862 Bothered by nausea C0007527 Cecal disease HSDN C4084776 Weight loss C0020725 Type ii mucolipidosis MalaCards|HPO C0015230 Exanthem C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0270948 Neurogenic muscular atrophy C1856304 Gsd iv, neuromuscular form, congenital MalaCards|HPO C3463815 Feel fatigue C0015461 Facial neoplasms HSDN C0000731 Abdomen distention C1563716 Thyroid dysgenesis HPO C1950154 Insomnia homeopathic medication C0085209 Bovine spongiform encephalitis MalaCards C4085317 Diarrhea frequency C0030922 Peptic ulcer hemorrhage HSDN C0033774 Skin pruritus C0031154 Peritonitis HSDN C0020305 Fetal edema C2930815 Acute cerebral gaucher disease MalaCards C2315100 Pediatric failure to thrive C3151058 Hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase HPO C4084725 Usual severity cough C0600467 Neurogenic inflammation HSDN C1963071 Back pain adverse event C0003507 Aortic valve stenosis HSDN C0014591 Bleeding nose C0035436 Rheumatic fever MalaCards C4084766 Vomiting C0040053 Thrombosis HSDN C0030193 Sense of pain C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C3873484 Xerostomia due to mouth breathing C0043352 Xerostomia UMLS C0497406 Over weight C0700208 Acquired scoliosis HSDN C0004134 Dyssynergia C0268263 Multiple sulfatase deficiency disease MalaCards|HPO|UMLS C0917816 Deficiency mental C1868311 Piebald trait neurologic defects OrphaNet|MalaCards C0003862 Pain joint C0032453 Polychondritis, relapsing MalaCards|HSDN C0042963 Symptoms vomiting C2981665 Stage ib distal bile duct cancer UMLS C4084784 Diarrhea C0273486 Cranial nerve x injury HSDN C4085661 Usual severity nausea C1552262 Nurse practitioner - family HSDN C2911647 Weight gain adverse event C0004238 Atrial fibrillation HSDN C0025287 Meningitis-like C0023364 Leptospirosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1522133 High cholesterol level HSDN C0034933 Abnormal reflexes C0034931 Reflex sympathetic dystrophy HSDN C2911645 Weight loss adverse event C1334928 Necrotic changes (finding) HSDN C0557874 Global developmental delay C0268542 Ornithine carbamoyltransferase deficiency HPO C4085661 Usual severity nausea C0018273 Growth disorders HSDN C3539023 Pelvic pain increasing in frequency C0009240 Cognition HSDN C0003862 Pain joint C1833699 Osteopoikilosis, isolated MalaCards C4085862 Bothered by nausea C0206062 Lung diseases, interstitial HSDN C0040264 Ear ringing sound C1622510 Neurocytoma MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0025309 Meningoencephalitis HSDN C3541349 Syncope C1962986 Glaucoma adverse event HSDN C0020538 Hbp C0019101 Hemorrhagic fever with renal syndrome MalaCards C0027066 Myoclonic jerking C0033873 Psychiatry HSDN C0232698 Abnormal defaecation C0267511 Constipation drug induced UMLS C2237041 Shox gene with short stature C1834818 Mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones HPO C3541349 Syncope C2676723 Jervell and lange-nielsen syndrome 2 (disorder) MalaCards|HPO C0032617 High urine output C0041972 Urethral obstruction HSDN C0015469 Facial paralysis C0010674 Cystic fibrosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242788 Breast neoplasms, male HSDN C0085602 Polydypsia C3489856 Cold hypersensitivity MalaCards C0024031 Back pain lower back C0006663 Calcinosis HSDN C0576456 Poor feeding C3539003 Neuropathy, hereditary sensory and autonomic, type vi MalaCards C0009792 Consciousness disorder C0002395 Alzheimer's disease HSDN C1279888 Proteinuria of undiagnosed cause C0029118 Opportunistic infections HSDN C0013362 Dysarthrias C1843014 Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques HPO C4085211 Pain distress question C0022572 Keratoacanthoma HSDN C0221263 Cafe au lait spot C0027832 Neurofibromatosis 2 HPO C4085211 Pain distress question C0035228 Respiratory hypersensitivity HSDN C3898969 Have been vomiting C0024535 Malaria, falciparum HSDN C0026826 High muscle tone C1859452 Microcephalic osteodysplastic primordial dwarfism, type i MalaCards C0012569 Double vision C0751815 Carotid artery, internal, dissection HSDN C0013404 Respiratory difficulty C2239253 Aneurysm of sinus of valsalva MalaCards C4050613 Anxiety C0221033 Trisomy x syndrome MalaCards C0242936 Center pain C0036220 Kaposi sarcoma HSDN C0030193 Sense of pain C0080233 Tooth loss HSDN C1963087 Constipation adverse event C0206245 Amyloid neuropathies, familial MalaCards|HSDN C0026821 Cramp C1837094 Myasthenic syndrome, congenital, ie MalaCards|HPO C4084788 Have dizziness C2609414 Acute kidney injury HSDN C0423004 Hyperaemia of surface of eye C0020452 Hyperemia UMLS C0000731 Abdomen distention C0036069 Saldino-noonan syndrome MalaCards C0012833 Dizzy C0015663 Fasting HSDN C0022346 Yellow skin C0597109 Nurse's role HSDN C0030193 Sense of pain C0560694 Bottles per feed HSDN C0011991 Loose stools C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO|UMLS C0007758 Cerebellar ataxia C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0018681 Headache, cephalalgia C1837218 Cleft palate, isolated HSDN C0575081 Abnormal gait C0393547 Bulbospinal neuronopathy OrphaNet|HPO C0034063 Edema lung C0268381 Primary amyloidosis OrphaNet|MalaCards C2984058 Have pain C0004114 Astrocytoma HSDN C2203646 Jaundice C0162568 Erythropoietic protoporphyria HSDN C4084767 Bothered by vomiting C0269291 Pregnancy heterotopic HSDN C1962972 Proteinuria adverse event C0008073 Developmental disabilities HSDN C0030193 Sense of pain C0032269 Pneumococcal infections HSDN C0242936 Center pain C0175754 Agenesis of corpus callosum HSDN C3463815 Feel fatigue C0032987 Ectopic pregnancy HSDN C2024878 Cardiovascular surgery result: dyspnea C0751674 Lymphangioleiomyomatosis OrphaNet|HPO|MalaCards C0206146 Myocardial stunning C0015190 Euthyroid sick syndromes HSDN C4084766 Vomiting C0338437 Neurocysticercosis HSDN C0018784 Deafness sensorineural C1537752 Mir96 gene HPO C0018834 Brash C4048800 Telomeric 22q13 monosomy syndrome MalaCards C2096293 Ent surgical result ear vertigo C0025286 Meningioma HSDN C3463815 Feel fatigue C0033788 Pseudo-hurler polydystrophy MalaCards C0032285 Pneum C1863239 Partial adenosine deaminase deficiency HPO C2237041 Shox gene with short stature C1859407 Bone dysplasia, lethal, holmgren type MalaCards C0751495 Seizure focal C0334228 Small cell tumor malignant UMLS C1963281 Vomiting adverse event C0036421 Systemic scleroderma HSDN C3539893 Pelvic pain occurs with intercourse C0033575 Prostatic diseases HSDN C4084768 Usual severity vomiting C0023530 Leukopenia HSDN C0221263 Cafe au lait spot C1857844 Williams-beuren region duplication syndrome MalaCards C4085222 Nausea C0011119 Decompression sickness HSDN C0015672 Decreased energy C0001175 Acquired immunodeficiency syndrome HSDN C0015230 Exanthem C0085273 Erythema infectiosum UMLS C0031911 Pigment deposition C0155359 Scleral staphyloma MalaCards C0085636 Light sensitivity C0027743 Nerve compression syndrome HSDN C0243026 Generalized infection C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C0027796 Neuralgias C2586211 Thrombosis of blood vessel HSDN C4084727 Cough frequency C0152937 Primary pneumonic plague DiseaseOntology|MalaCards C0027796 Neuralgias C0011849 Diabetes mellitus HSDN C0040034 Thrombocytopenia C3281001 Wiskott-aldrich syndrome 2 MalaCards C1260880 Nasal drip C0862752 Nasopharyngeal undifferentiated carcinoma stage o UMLS C0557874 Global developmental delay C0878677 Glycogen storage disease type iib MalaCards|HPO C0040822 D tremors C1263846 Attention deficit hyperactivity disorder HSDN C0026826 High muscle tone C0033578 Prostatic neoplasms HSDN C0011991 Loose stools C0021053 Immune system diseases HSDN C0575081 Abnormal gait C0037773 Spastic paraplegia, hereditary OrphaNet|MalaCards C4084774 Have weight loss C0037274 Dermatologic disorders HSDN C0020458 Hyperhydrosis C1334968 Nodular lymphocyte predominant hodgkin lymphoma MalaCards C0033377 Caudal displacement C0796083 Najjar syndrome OrphaNet|HPO C2017342 Soft tissue swelling r hand between ring and little finger C0037580 Soft tissue swelling UMLS C0036572 Convulsion C3840267 Epilepsy in childbirth UMLS C0030552 Paralysis partial C0265294 Pyle metaphyseal dysplasia MalaCards|HPO C0002170 Alopecia disorders C0406723 Growth retardation, alopecia, pseudoanodontia and optic atrophy OrphaNet|HPO|MalaCards C0242936 Center pain C0032987 Ectopic pregnancy HSDN C3539889 Pelvic pain increasing in severity C0205788 Histiocytoid hemangioma HSDN C0007758 Cerebellar ataxia C0338586 Vertebral artery dissection HSDN C0011168 Disorder deglutition C1846058 Lubs x-linked mental retardation syndrome HPO C0349588 Stature short C1859432 Blepharophimosis with ptosis, syndactyly, and short stature OrphaNet|MalaCards C0018681 Headache, cephalalgia C0021818 Intervertebral disk displacement HSDN C0019079 Bloody sputum C1336172 Stage iia small cell carcinoma of lung UMLS C2242996 Tingling C0152244 Bone cysts, aneurysmal HSDN C1963065 Apnea adverse event C3550273 Peroxisome biogenesis disorder 2a (zellweger) MalaCards C0018681 Headache, cephalalgia C1861785 Cavernous malformations of cns and retina HPO C2024878 Cardiovascular surgery result: dyspnea C0019326 Ventral hernia HSDN C4084723 Constipation C0343375 A; paratyphoid fever DiseaseOntology|MalaCards C0002622 Amnesias C0376542 Cognitive science HSDN C3641756 Have diarrhea C1134719 Invasive ductal breast carcinoma HSDN C0413252 Hypothermia due to exposure C0011265 Presenile dementia HSDN C3641756 Have diarrhea C0439840 Reflex motion descriptor HSDN C4084724 Usual severity constipation C0003857 Congenital arteriovenous malformation HSDN C1069915 Vertigo C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0027066 Myoclonic jerking C4225350 Epileptic encephalopathy, early infantile, 32 UMLS C4085210 Usual severity pain C0282607 Vascular neoplasms HSDN C0009806 Constipate C2936913 Porphyria, south african type HPO C1549543 Administration method - pain C2616767 Mycetoma HSDN C4085211 Pain distress question C0393571 Multiple system atrophy HSDN C2984058 Have pain C0079027 Blood loss, surgical HSDN C0684343 Pseudophakia C1963266 Uveitis adverse event HSDN C0020673 Hypothermia (central) (local) C0376618 Endotoxemia HSDN C4084767 Bothered by vomiting C0025149 Medulloblastoma HSDN C0231341 Aging premature C0027804 Fatigue neurosis HSDN C0013404 Respiratory difficulty C1455705 Pulmonary histiocytosis x OrphaNet|MalaCards C0004604 Pain back C0007131 Non-small cell lung carcinoma HSDN C1069915 Vertigo C1522133 High cholesterol level HSDN C0004134 Dyssynergia C1412084 Abcd1 gene HSDN C4085661 Usual severity nausea C0497327 Dementia HSDN C1963252 Tremor adverse event C0034530 Injury radiation HSDN C0036572 Convulsion C3554002 Pbd12a MalaCards C0006370 Bulimia C0270611 Brain damage HSDN C0036659 Sensation disorder C0021308 Infarction HSDN C1260880 Nasal drip C0280334 Epidermoid carcinoma of paranasal sinus UMLS C1963077 Bone pain adverse event C0268250 Gaucher disease, type 2 (disorder) MalaCards C0013604 Edematous C0031212 Personality disorders HSDN C0003126 Smell loss C2749346 Refsum disease, adult, 2 HPO C0013404 Respiratory difficulty C0039494 Temporomandibular joint disorders HSDN C3898969 Have been vomiting C0023487 Acute promyelocytic leukemia HSDN C1557397 Adverse event associated with pain C0270327 Bedwetting HSDN C1535893 Orthostatic intolerance C0037929 Spinal cord injuries HSDN C0042963 Symptoms vomiting C3665596 Warts HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0029118 Opportunistic infections HSDN C3887638 Failure to thrive in infant C1421354 Umps gene HPO C1384666 Decreased hearing C0036341 Schizophrenia HSDN C0042571 Vertigo subjective C0282507 Heat stress disorders HSDN C4085210 Usual severity pain C0560651 Spinal cord syndrome central HSDN C3539022 Pelvic pain decreasing in severity C1550672 Specimen type - ulcer HSDN C2984057 Have nausea C0013292 Obstruction duodenal HSDN C0003811 Cardiac rhythm disturbance C0039483 Giant cell arteritis MalaCards C0520586 Dryness of vulva C0042994 Vulvar diseases UMLS C4085661 Usual severity nausea C0022568 Keratitis HSDN C0242936 Center pain C0014474 Ependymoma HSDN C2895042 Pain in left elbow C0810055 Other non-traumatic joint disorders UMLS C0036572 Convulsion C0175704 Leopard syndrome MalaCards C3494358 Characteristic, prodromal C0011269 Dementia, vascular HSDN C0004604 Pain back C0001080 Achondroplasia HSDN C1565249 Limitation, mobility C0009404 Colorectal neoplasms HSDN C1963252 Tremor adverse event C0334123 Histiocytosis, lipoid MalaCards C0013604 Edematous C0751651 Mitochondrial diseases HSDN C3829611 Nausea frequency C0022650 Kidney calculi HSDN C0002965 Crescendo angina C0009450 Disease caused by microorganism HSDN C2024878 Cardiovascular surgery result: dyspnea C0273115 Lung injury HSDN C3539892 Pelvic pain in front C0033575 Prostatic diseases HSDN C1145670 Failure respiratory C1864947 Natural killer cell deficiency, familial isolated HPO C0038002 Spleen enlargement C3179455 Niemann-pick disease, type c1 MalaCards|HPO C0027498 Nausea vomiting C1535939 Pneumocystis jiroveci pneumonia UMLS C0009398 Color vision defects C0023343 Leprosy HSDN C1557397 Adverse event associated with pain C0042749 Viremia HSDN C1279888 Proteinuria of undiagnosed cause C2931667 Fitzsimmons walson mellor syndrome MalaCards C0040822 D tremors C0002871 Anemia HSDN C0857305 Thrombocytopenia purpura C0042138 Uterine neoplasms HSDN C4084774 Have weight loss C2936881 Eosinophilic synovitis MalaCards C0015672 Decreased energy C0029408 Degenerative polyarthritis HSDN C0030193 Sense of pain C0878588 Sphincter oddi dysfunction HSDN C0026838 Spasticity muscle C0016542 Foreign body HSDN C0085128 Cardiac output elevated C0043255 Stab wound HSDN C2203646 Jaundice C0019087 Hemorrhagic disorders HSDN C0424755 Fever symptoms C0039971 Thirst HSDN C0239134 Cough productive C1535939 Pneumocystis jiroveci pneumonia UMLS C0013404 Respiratory difficulty C0033586 Failure, prosthesis HSDN C0162298 Stiffness joints C0877753 Stiffness of joint, nec, involving lower leg in mdr19_0 UMLS C1549543 Administration method - pain C0039263 Takayasu arteritis HSDN C1549543 Administration method - pain C0221204 Lytic lesion HSDN C0007166 Cardiac output decreased C0038941 Incisional infection HSDN C0231791 In toe C1834523 Arthrogryposis, distal, type 2b MalaCards|HPO C3641756 Have diarrhea C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C0231218 Malaise generalized C3898888 Bclc staging for hepatocellular carcinoma UMLS C0007758 Cerebellar ataxia C0029124 Optic atrophy MalaCards C1963252 Tremor adverse event C0022408 Arthropathy HSDN C0518090 Frequency of pain question C0752155 Central nervous system vascular malformations HSDN C0039870 Leanness C0037410 Social discrimination HSDN C0023380 Lethargy C1720922 Respiratory aspiration HSDN C0015672 Decreased energy C0005940 Bone diseases HSDN C0427068 Legs weakness C1762616 Meningioma, benign, no icd-o subtype MalaCards C2919142 Short stature adverse event C0796070 Microphthalmia, syndromic 7 MalaCards|HPO C4084769 Vomiting frequency C0085094 Head injury closed HSDN C0012833 Dizzy C0038354 Stomach diseases HSDN C0018681 Headache, cephalalgia C0023530 Leukopenia HSDN C0575081 Abnormal gait C1846058 Lubs x-linked mental retardation syndrome OrphaNet|HPO C0008031 Pain chest C0010346 Crohn disease HSDN C0917816 Deficiency mental C2931488 Zlotogora-ogur syndrome OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C0035435 Rheumatism HSDN C0038990 Sweats C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C0013421 Dystonia C2678194 Mental retardation, x-linked, syndromic, christianson type OrphaNet|HPO C1963154 Renal failure adverse event C1857662 Coach syndrome MalaCards C1963252 Tremor adverse event C1963119 Stomach ulcer adverse event HSDN C0746674 Muscle weakness generalized C0021670 Insulinoma OrphaNet|HPO|MalaCards C3887873 Hearing loss C3542413 Cdisc adas-cog - comprehension HSDN C0234146 Absent reflex C0393807 Hereditary motor and sensory neuropathy with optic atrophy (disorder) HPO C0424755 Fever symptoms C1849386 Myoglobinuria, acute recurrent, autosomal recessive MalaCards|HPO C0013604 Edematous C1456784 Paranoia HSDN C0917816 Deficiency mental C1849128 Spastic paraplegia 15, autosomal recessive MalaCards|HPO C0332573 Macula C1851481 Erythrokeratodermia with ataxia OrphaNet|HPO C4085211 Pain distress question C1522057 Acute enteritis of the mouse intestinal tract HSDN C1963065 Apnea adverse event C1522136 Hypernatremia result HSDN C4085222 Nausea C3714514 Infection HSDN C0015676 Mental fatigue C0877792 Sleep disorders, circadian rhythm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023896 Alcoholic liver diseases HSDN C0018772 Deafness C0026848 Myopathy HSDN C0242936 Center pain C0022134 Islet cell adenoma HSDN C0019209 Large liver C3808940 Lipodystrophy, familial partial, type 5 MalaCards C4085222 Nausea C0014868 Esophagitis HSDN C4084776 Weight loss C0006264 Bronchial neoplasms HSDN C1384666 Decreased hearing C0021345 Infectious mononucleosis MalaCards C1549543 Administration method - pain C0022134 Islet cell adenoma HSDN C1549543 Administration method - pain C1456865 Ureteral calculi HSDN C4084774 Have weight loss C0007130 Mucinous adenocarcinoma HSDN C0036572 Convulsion C0281865 Hip injury HSDN C0231218 Malaise generalized C0278696 Childhood hepatoma, group i UMLS C2024878 Cardiovascular surgery result: dyspnea C0029411 Osteoarthropathy, primary hypertrophic HSDN C0027066 Myoclonic jerking C0031154 Peritonitis HSDN C4084802 Usual severity diarrhea C0038362 Stomatitis HSDN C0424755 Fever symptoms C0019270 Hernia HSDN C1963249 Tinnitus adverse event C0037942 Spinal osteophytosis HSDN C0013428 Painful urination C0855189 Stage ii bladder squamous cell carcinoma UMLS C0344315 Mood depressed C1439329 Cbs gene HPO C0036572 Convulsion C0751523 Non convulsive status epilepticus UMLS C0027066 Myoclonic jerking C1968556 Encephalopathy, neonatal severe, due to mecp2 mutations HPO|UMLS C0002962 Angina C1963198 Pancreatitis adverse event HSDN C1961131 Cough adverse event C0027439 Nasopharyngeal neoplasms HSDN C0018524 Hallucinate C0002736 Amyotrophic lateral sclerosis HSDN C0242936 Center pain C0020461 Hyperkalemia HSDN C0012833 Dizzy C1556682 Adverse event associated with infection HSDN C0497247 Blood pressure elevation C0950122 Frasier syndrome MalaCards C0042571 Vertigo subjective C0023290 Leishmaniasis, visceral HSDN C2911645 Weight loss adverse event C0349464 Wernicke-korsakoff syndrome HSDN C0030554 Abnormal sensation C0025286 Meningioma HSDN C2024893 Cardiovascular surgery result: fatigue C1136033 Cutaneous mastocytosis MalaCards C0151786 Weakness muscle C0017168 Gastroesophageal reflux disease HSDN C0497406 Over weight C0016658 Fracture bone HSDN C0035229 Respiratory function impaired C0520681 Central alveolar hypoventilation syndrome MalaCards C0006370 Bulimia C0020538 Hypertensive disease HSDN C0027066 Myoclonic jerking C0221065 Subacute combined degeneration HSDN C2919142 Short stature adverse event C2930852 Zellweger leukodystrophy MalaCards C4084726 Distress cough C0001973 Alcoholic intoxication, chronic HSDN C4084788 Have dizziness C0011570 Mental depression HSDN C4085862 Bothered by nausea C2240378 Cleft palate on exam HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018790 Cardiac arrest HSDN C0026838 Spasticity muscle C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C1962957 Flushing adverse event C1306571 Hepatic insufficiency HSDN C4085211 Pain distress question C0031099 Periodontitis HSDN C0036572 Convulsion C3150172 Mtdps8b MalaCards|HPO C0043144 Wheeze C0006271 Bronchiolitis MalaCards C0086565 Liver function abnormal C0024620 Primary malignant neoplasm of liver MalaCards C0518090 Frequency of pain question C0003490 Aortic arch syndrome HSDN C0032617 High urine output C0037286 Skin neoplasms HSDN C0151686 Growth retardation C0574083 3-methylglutaconic aciduria type 2 MalaCards|HPO C4084768 Usual severity vomiting C0010356 Cross infection HSDN C4084726 Distress cough C0206629 Pulmonary blastoma OrphaNet|HSDN|MalaCards C0232466 Feeding difficulty C0796033 Marden-walker syndrome MalaCards C2029884 Hearing loss by exam C1138434 Disease, x-linked genetic HSDN C0426579 Anorexia symptom C0018671 Head and neck neoplasms HSDN C4084768 Usual severity vomiting C0520946 Emotional hypersensitivity HSDN C4084767 Bothered by vomiting C0852654 21-hydroxylase deficiency MalaCards C0018772 Deafness C0003090 Ankylosis HSDN C0018524 Hallucinate C0038819 Siriasis HSDN C0423721 Painful arms and moving fingers C1527351 Nerve root disorder UMLS C2203646 Jaundice C0018671 Head and neck neoplasms HSDN C0016199 Pain flank C0020649 Hypotension HSDN C0005745 Blepharoptosis C1855904 Acrofrontofacionasal dysostosis 2 MalaCards C4085862 Bothered by nausea C1306577 Dies patient HSDN C0151786 Weakness muscle C0021843 Intestinal obstruction HSDN C2024878 Cardiovascular surgery result: dyspnea C0011882 Diabetic neuropathies HSDN C0014591 Bleeding nose C0019080 Hemorrhage MalaCards C4084774 Have weight loss C0025517 Metabolic diseases HSDN C4085317 Diarrhea frequency C3281289 Trichohepatoenteric syndrome 2 MalaCards C0917816 Deficiency mental C1855722 Iris coloboma with ptosis, hypertelorism, and mental retardation MalaCards|HPO C0812426 Kidney problem C0004775 Bartter disease UMLS C0542476 Forgetful C3807295 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant MalaCards C0151908 Dry skin C0406645 Amyopathic dermatomyositis MalaCards C4084723 Constipation C0001144 Acne vulgaris HSDN C2024878 Cardiovascular surgery result: dyspnea C0001618 Tumors of adrenal cortex HSDN C0030193 Sense of pain C0008497 Choriocarcinoma HSDN C4084769 Vomiting frequency C0041956 Ureteral obstruction HSDN C3898969 Have been vomiting C0338437 Neurocysticercosis HSDN C0020455 Hypergammaglobulinemia C0023290 Leishmaniasis, visceral HSDN C0851578 Disorder sleep C0023676 Life style HSDN C1963063 Anorexia adverse event C0235782 Gallbladder carcinoma OrphaNet C0000737 Abdomen pain C1706732 Advanced adult hepatocellular carcinoma UMLS C4085210 Usual severity pain C0021345 Infectious mononucleosis HSDN C0332573 Macula C0343829 Macular yaws UMLS C1971624 Appetite absent C0021368 Inflammation HSDN C1279888 Proteinuria of undiagnosed cause C0002989 Epithelioid hemangioma of skin HSDN C0349588 Stature short C0175701 Aarskog syndrome OrphaNet|HPO|MalaCards C0237326 Defecation pain C2931939 Idiopathic orthostatic hypotension MalaCards C2024893 Cardiovascular surgery result: fatigue C0030521 Parathyroid neoplasms MalaCards C1557397 Adverse event associated with pain C0079731 B-cell lymphomas HSDN C0042571 Vertigo subjective C0009373 Colonic diseases HSDN C0013395 Indigestion C0314657 Genetic predisposition HSDN C0033790 Pseudobulbar palsy C0270736 Essential tremor HSDN C0518090 Frequency of pain question C0011989 Camurati-engelmann syndrome HSDN C0030486 Extremity paralysis, lower C0035222 Respiratory distress syndrome, adult HSDN C0042963 Symptoms vomiting C1275081 Cardio-facio-cutaneous syndrome HPO|UMLS C0020672 Body temperature decreased C0014859 Esophageal neoplasms HSDN C1961131 Cough adverse event C0004161 Athletic injuries HSDN C0022346 Yellow skin C0524910 Hepatitis c, chronic MalaCards|HSDN C0020796 Profoundly mentally retarded C0393591 Aicardi-goutieres syndrome OrphaNet|HPO|MalaCards C4084784 Diarrhea C0241158 Cicatrix skin HSDN C1963087 Constipation adverse event C0014836 Escherichia coli infections HSDN C0150055 Pain chronic C0011882 Diabetic neuropathies HSDN C4084773 Bothered by weight gain C0042485 Venous insufficiency HSDN C3815497 Cough C0004153 Atherosclerosis HSDN C1579931 Depressed - symptom C0268322 Chester-type porphyria HPO C0233514 Behavior abnormal C0796275 Brunner syndrome OrphaNet|HPO|MalaCards C0040259 Tinea pedis C0042373 Vascular diseases HSDN C0242936 Center pain C0036918 Sexually transmitted diseases, viral HSDN C4084788 Have dizziness C1579931 Depressed - symptom HSDN C4084723 Constipation C0015579 Family characteristics HSDN C2203646 Jaundice C2930852 Zellweger leukodystrophy MalaCards C0520909 Ponv C0027765 Nervous system disorder HSDN C0041657 Consciousness loss C0011570 Mental depression HSDN C0000737 Abdomen pain C0242666 Protein s deficiency HSDN C0031911 Pigment deposition C0153628 Malignant neoplasm of conjunctiva MalaCards C2037122 Sudden loss left vision C2037137 Sudden loss left vision left UMLS C0013362 Dysarthrias C2586211 Thrombosis of blood vessel HSDN C0020673 Hypothermia (central) (local) C0006261 Bronchial diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0011854 Diabetes mellitus, insulin-dependent HSDN C1860844 Sparse, thin hair C0268647 Lysinuric protein intolerance MalaCards|HPO|UMLS C0000727 Abdomen acute C0013504 Echinococcosis, hepatic HSDN C4085210 Usual severity pain C0162739 Hellp syndrome HSDN C1963281 Vomiting adverse event C0009319 Colitis HSDN C0521516 Polymyalgia C1533847 Disorder of skeletal muscle UMLS C0030486 Extremity paralysis, lower C0016507 Acquired foot deformities HSDN C4085211 Pain distress question C0037072 Diseases sigmoid HSDN C4084767 Bothered by vomiting C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C2984058 Have pain C0025500 Mesothelioma HSDN C2024878 Cardiovascular surgery result: dyspnea C0041834 Erythema HSDN C2096293 Ent surgical result ear vertigo C0027663 Neoplasms, multiple primary HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019348 Herpes simplex infections HSDN C0026838 Spasticity muscle C0700208 Acquired scoliosis HSDN C4084773 Bothered by weight gain C0023976 Long qt syndrome HSDN C0234132 Pyramidal sign C0751603 Autosomal recessive hereditary spastic paraplegia MalaCards C0015676 Mental fatigue C0027651 Tumor HSDN C1963087 Constipation adverse event C0035243 Respiratory tract infections HSDN C0015230 Exanthem C1304456 Congo hemorrhagic fever MalaCards C2984057 Have nausea C0027947 Neutropenia HSDN C0002962 Angina C0011142 Defense mechanism HSDN C0349588 Stature short C3150215 Chromosome 6q24-q25 deletion syndrome MalaCards C0242936 Center pain C0039130 Cardiovascular syphilis HSDN C0018784 Deafness sensorineural C1847626 Deafness, autosomal dominant 36 MalaCards|HPO C0032617 High urine output C1000483 Genus anemia HSDN C1963093 Dizziness adverse event C0079744 Diffuse large b-cell lymphoma HSDN C2984058 Have pain C1963235 Sick sinus syndrome adverse event HSDN C4084775 Usual severity weight loss C0023860 Listeriosis HSDN C2096293 Ent surgical result ear vertigo C0004153 Atherosclerosis HSDN C0234146 Absent reflex C2930997 Congenital disorder of glycosylation type 1c MalaCards C0013456 Pain ear C0149722 Hutchinson's melanotic freckle HSDN C3665347 Vision impaired C1859773 Microphthalmia, syndromic 3 OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C1705810 Generic role HSDN C0018772 Deafness C0149721 Left ventricular hypertrophy HSDN C1549543 Administration method - pain C0007274 Carotid artery thrombosis HSDN C4085549 Dizziness C0024841 Matrimony, matrimonial HSDN C1963091 Diarrhea adverse event C0005659 Bite sting HSDN C0036659 Sensation disorder C0002768 Congenital pain insensitivity HSDN C0027497 Queasy C0085183 Neoplasms, second primary HSDN C0162834 Hyperpigmentation C0162361 Hidrotic ectodermal dysplasia HPO C0000727 Abdomen acute C1263960 Diabetic coma HSDN C3887873 Hearing loss C1546949 Event consequence - death HSDN C4042891 Sleep wake disorders C0006107 Concussion HSDN C2984058 Have pain C0043254 Injuries penetrating HSDN C2017207 Soft tissue swelling l hand between thumb and index finger C0037580 Soft tissue swelling UMLS C0740584 Abdomen pain diffuse C1848586 Intestinal pseudoobstruction with external ophthalmoplegia MalaCards|UMLS C0231528 Muscle pain generalized C0343633 Brazilian haemorrhagic fever MalaCards C0019079 Bloody sputum C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0015302 External exotoses HSDN C1963087 Constipation adverse event C0243026 Sepsis HSDN C4085222 Nausea C0019693 Hiv infections HSDN C0232466 Feeding difficulty C0016952 Galactosemias MalaCards C0518090 Frequency of pain question C0848558 Hypospadias HSDN C4084775 Usual severity weight loss C0042487 Venous thrombosis HSDN C0085593 Chill C0025202 Melanoma HSDN C0029844 Other spec.visual disturb.nos C0809996 Blindness and vision defects UMLS C0006370 Bulimia C3542996 Mindfulness HSDN C0727671 Red cross toothache drops C0014544 Epilepsy HSDN C4084725 Usual severity cough C0206703 Carcinoma, giant cell HSDN C4084774 Have weight loss C0085278 Antiphospholipid syndrome HSDN C2024893 Cardiovascular surgery result: fatigue C0022408 Arthropathy HSDN C1557397 Adverse event associated with pain C0034628 Radius fracture HSDN C3665346 Loss sight C1527406 Rhizomelic pseudopolyarthritis MalaCards C2315100 Pediatric failure to thrive C0022584 Keratoderma, palmoplantar, diffuse HSDN C0004604 Pain back C0242216 Biliary calculi HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013514 Echinostomiasis DiseaseOntology C0004604 Pain back C0042826 Field visual HSDN C1557397 Adverse event associated with pain C0003860 Arteritis HSDN C0023530 Leukopenia C0268543 Hyperammonemia, type iii MalaCards C1000483 Genus anemia C0878675 Erdheim-chester disease MalaCards C2024893 Cardiovascular surgery result: fatigue C0017205 Gaucher disease OrphaNet|MalaCards C4084768 Usual severity vomiting C1833104 Diabetes mellitus, permanent neonatal MalaCards C3898969 Have been vomiting C3665493 Snake bites HSDN C3898969 Have been vomiting C0017536 Giardiasis DiseaseOntology|HSDN C2911647 Weight gain adverse event C0038362 Stomatitis HSDN C0018989 Paresis of one side of body C2675650 Brain small vessel disease with axenfeld rieger anomaly HPO C1519353 Skin eruption papular C3812646 Drug induced cutaneous vasculitis MalaCards C1963066 Joint pain adverse event C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C2024878 Cardiovascular surgery result: dyspnea C1862939 Amyotrophic lateral sclerosis 1 MalaCards C2919142 Short stature adverse event C0796037 Martsolf syndrome OrphaNet|HPO|MalaCards C0042818 Visual discomfort, nos C0034951 Refractive errors UMLS C0237326 Defecation pain C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0009806 Constipate C2239176 Liver carcinoma HSDN C4084724 Usual severity constipation C0014170 Endometrial neoplasms HSDN C0030552 Paralysis partial C0162532 Variegate porphyria MalaCards|HPO C0018772 Deafness C1861735 Dementia, familial danish HPO C1565249 Limitation, mobility C0008625 Chromosome aberrations HSDN C1963093 Dizziness adverse event C0013808 Electroconvulsive therapy HSDN C0151825 Ostalgia C0917715 Hajdu-cheney syndrome OrphaNet|HPO C4084802 Usual severity diarrhea C2911243 Encounter due to family history of colonic polyps HSDN C2911645 Weight loss adverse event C0302280 Adrenogenital syndrome HSDN C0018681 Headache, cephalalgia C0334581 Gemistocytic astrocytoma UMLS C0013604 Edematous C0038814 Sunburn HSDN C1557397 Adverse event associated with pain C0023176 Lead poisoning HSDN C0011991 Loose stools C0018995 Hemochromatosis HSDN C0011991 Loose stools C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0011991 Loose stools C0011854 Diabetes mellitus, insulin-dependent HSDN C0038506 Stutter C0017400 Behavioral genetics HSDN C2911647 Weight gain adverse event C0016514 Foot-and-mouth disease HSDN C0026826 High muscle tone C1848199 X-linked lissencephaly OrphaNet|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0027927 Neurosyphilis HSDN C0013604 Edematous C0525045 Mood disorders HSDN C0009806 Constipate C0008370 Cholestasis HSDN C0575081 Abnormal gait C2931828 Keratoderma and spastic paralysis MalaCards C1963180 Neck pain adverse event C0030305 Pancreatitis HSDN C4085317 Diarrhea frequency C0162565 Acute intermittent porphyria MalaCards|HPO C0026884 Muteness C0014059 Encephalomyelitis, acute disseminated HSDN C0010200 Cough symptom C0948089 Acute coronary syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0853986 Lymphocytes decreased HSDN C4085862 Bothered by nausea C0040053 Thrombosis HSDN C0349588 Stature short C2936915 Amylo-1,6-glucosidase deficiency OrphaNet|HPO C2237041 Shox gene with short stature C0338503 Septo-optic dysplasia OrphaNet|HPO|MalaCards C0007859 Pain neck C0027831 Neurofibromatosis 1 HSDN C0003962 Ascites C2931758 Acquired angioedema MalaCards C0006370 Bulimia C0015726 Focused anxiety HSDN C4084767 Bothered by vomiting C0013336 Dwarfism HSDN C4085211 Pain distress question C0028840 Ocular hypertension HSDN C0026838 Spasticity muscle C2936907 Nadh:q(1) oxidoreductase deficiency MalaCards|HPO C4084726 Distress cough C0014858 Esophageal motility disorders HSDN C0020458 Hyperhydrosis C0175693 Russell-silver syndrome MalaCards C4084775 Usual severity weight loss C0085407 Infection by cnidospora, nos HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206647 Dermatofibrosarcoma HSDN C0018681 Headache, cephalalgia C1548483 Leishmaniasis vaccine HSDN C0042024 Urine incontinence C0031212 Personality disorders HSDN C4084802 Usual severity diarrhea C0003493 Aortic diseases HSDN C0013456 Pain ear C0020538 Hypertensive disease HSDN C0152116 Torticollis spasmodic C4075597 Spasmodic torticolis as late effect of trauma UMLS C2024893 Cardiovascular surgery result: fatigue C2347126 Microscopic polyarteritis HSDN C4084766 Vomiting C0031117 Peripheral neuropathy HSDN C1963071 Back pain adverse event C0032019 Pituitary neoplasms HSDN C1549543 Administration method - pain C0020875 Ileal diseases HSDN C1565249 Limitation, mobility C0023974 Loneliness HSDN C0030193 Sense of pain C0043407 Yersinia infections HSDN C0004941 Behavioral symptoms C0233523 Antisocial behavior MalaCards C4084725 Usual severity cough C0014236 Endophthalmitis HSDN C0221263 Cafe au lait spot C0029422 Osteochondrodysplasias HSDN C0026838 Spasticity muscle C2960129 Vanishing white matter disease MalaCards C2029884 Hearing loss by exam C0027439 Nasopharyngeal neoplasms HSDN C1000483 Genus anemia C1856603 Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to OrphaNet|HPO C0005745 Blepharoptosis C2930913 Chromosome 13q deletion MalaCards C2024893 Cardiovascular surgery result: fatigue C0023281 Leishmaniasis MalaCards C1557397 Adverse event associated with pain C0017075 Ganglioneuroma HSDN C4085210 Usual severity pain C0032580 Adenomatous polyposis coli HSDN C0020450 Hyperemesis gravidarum C0042138 Uterine neoplasms HSDN C4085317 Diarrhea frequency C0005586 Bipolar disorder HSDN C0518090 Frequency of pain question C0751922 Median neuropathy HSDN C3641756 Have diarrhea C0887833 Carcinoma, pancreatic ductal HSDN C0030232 Color loss C0272051 Xerocytosis HPO C0012833 Dizzy C0003493 Aortic diseases HSDN C0015676 Mental fatigue C1963064 Anxiety adverse event HSDN C0018681 Headache, cephalalgia C0041330 Tuberculosis, spinal HSDN C0039070 Collapse fleeting C3150953 Long qt syndrome 6 MalaCards|HPO|UMLS C1961131 Cough adverse event C0012691 Dislocations HSDN C4085210 Usual severity pain C0017160 Gastroenteritis HSDN C0030552 Paralysis partial C2749864 Mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MalaCards C1963064 Anxiety adverse event C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C1838579 Pseudobulbar signs C4022811 Abnormality of nervous system physiology UMLS C3641756 Have diarrhea C0035242 Respiratory tract diseases HSDN C0030193 Sense of pain C0018572 Hand, foot and mouth disease HSDN C0004941 Behavioral symptoms C0796085 Nance-horan syndrome MalaCards|HPO C4085210 Usual severity pain C0013505 Cyst, pulmonary hydatid HSDN C0004134 Dyssynergia C1970270 Choreoathetosis and congenital hypothyroidism HPO C0277959 Hair coarseness C1839311 Scott bryant graham syndrome OrphaNet|MalaCards C2032396 Pelvic pain on the right C1963088 Cystitis adverse event HSDN C0003550 Broca aphasia C0007760 Cerebellar diseases HSDN C0700078 Deep tendon reflex decrease C2678015 Myopathy, reducing body, x-linked, childhood-onset HPO C0004604 Pain back C0017152 Gastritis HSDN C1557397 Adverse event associated with pain C0040436 Dental erosion HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032131 Plasmacytoma HSDN C2984058 Have pain C0040247 Tinea HSDN C2362324 Pediatric obesity C0019693 Hiv infections HSDN C2911647 Weight gain adverse event C0014852 Esophageal diseases HSDN C0150045 Urinary incontinence urge C0032962 Pregnancy complications HSDN C2911645 Weight loss adverse event C0007134 Renal cell carcinoma HSDN C3463815 Feel fatigue C0015457 Expression facial HSDN C1963093 Dizziness adverse event C0032343 Poisoning HSDN C1549543 Administration method - pain C0001768 Agammaglobulinemia HSDN C0000737 Abdomen pain C0021359 Infertility HSDN C0424755 Fever symptoms C0005695 Bladder neoplasm HSDN C4085548 Usual severity dizziness C0025427 Mercury poisoning HSDN C0037771 Paraparesis spastic C0019114 Hemosiderosis HSDN C3463815 Feel fatigue C0265265 Aase syndrome MalaCards C0024031 Back pain lower back C0033677 Protein-energy malnutrition HSDN C4084802 Usual severity diarrhea C4015214 Autoimmune lymphoproliferative syndrome, type v MalaCards C0009421 Comatose C0007787 Transient ischemic attack HSDN C4084768 Usual severity vomiting C0041228 African trypanosomiasis HSDN C4085317 Diarrhea frequency C0206718 Ganglioneuroblastoma HSDN C0851578 Disorder sleep C0017152 Gastritis HSDN C1963091 Diarrhea adverse event C0019104 Hemorrhagic fevers, viral OrphaNet|MalaCards C0557874 Global developmental delay C3151126 Meier-gorlin syndrome 5 HPO C2237041 Shox gene with short stature C3279941 Stickler syndrome, type iv MalaCards C0015672 Decreased energy C0002949 Aneurysm, dissecting HSDN C0018772 Deafness C3468041 Fanconi anemia, complementation group c MalaCards C4084802 Usual severity diarrhea C0268384 Familial amyloid neuropathy, portuguese type MalaCards C0241462 Tooth heat sensitivity C0011432 Dentin hypersensitivity UMLS C0851578 Disorder sleep C0039474 Temperament HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0017525 Giant cell tumors HSDN C0206146 Myocardial stunning C0003873 Rheumatoid arthritis HSDN C4085210 Usual severity pain C0000833 Abscess HSDN C1963154 Renal failure adverse event C1865794 Rhyns syndrome MalaCards C0700590 Diaphoresis excessive C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C1962972 Proteinuria adverse event C1857395 De toni-debre-fanconi syndrome HPO C0031911 Pigment deposition C0027665 Neoplasms, nerve tissue MalaCards C0018772 Deafness C0038661 Suicide HSDN C0015469 Facial paralysis C0024958 Maxillary sinus neoplasms HSDN C0030193 Sense of pain C4041132 Phantom pain following amputation of penis UMLS C0042963 Symptoms vomiting C0002940 Aneurysm HSDN C1963071 Back pain adverse event C0015397 Disorder of eye HSDN C3887638 Failure to thrive in infant C0030779 Pelger-huet anomaly MalaCards|HPO C0036572 Convulsion C1333597 Cerebral falx meningioma UMLS C0019209 Large liver C4048826 Mud fever MalaCards C0557874 Global developmental delay C1832736 Congenital disorder of glycosylation, type id OrphaNet|HPO|MalaCards C0020458 Hyperhydrosis C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0518090 Frequency of pain question C0031142 Peritoneal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085392 Bacteroidaceae infection HSDN C0036572 Convulsion C0751955 Brain infarction HSDN C4085211 Pain distress question C0152814 Epididymal tuberculosis MalaCards C0036659 Sensation disorder C2985290 Fetal alcohol spectrum disorders HSDN C4085210 Usual severity pain C0396023 Chronic adenoiditis DiseaseOntology|MalaCards C0012833 Dizzy C0040053 Thrombosis HSDN C1963252 Tremor adverse event C1704436 Peripheral arterial diseases HSDN C1557397 Adverse event associated with pain C2963140 Arteriovenous fistula in use with two needles HSDN C0520909 Ponv C0004238 Atrial fibrillation HSDN C0242936 Center pain C0034888 Rectal prolapse HSDN C0036572 Convulsion C3887608 Hydrocephalus, nonsyndromic, autosomal recessive 1 MalaCards|UMLS C0039070 Collapse fleeting C0949570 Allergies wheat HSDN C0231712 Gait waddling C0220743 Childhood hypophosphatasia (disorder) MalaCards|HPO|UMLS C1557397 Adverse event associated with pain C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C3665347 Vision impaired C0796028 Ataxia, fatal x-linked, with deafness and loss of vision OrphaNet|HPO|MalaCards C0242936 Center pain C0042384 Vasculitis HSDN C4084726 Distress cough C0282607 Vascular neoplasms HSDN C3641756 Have diarrhea C0016169 Pathologic fistula HSDN C3539893 Pelvic pain occurs with intercourse C0042341 Varicocele HSDN C0040034 Thrombocytopenia C0431406 Asymmetric crying face association HPO C0030193 Sense of pain C0015630 Fantasies HSDN C0013911 Emaciate C0034531 Experimental radiation injuries HSDN C0151311 Cranial nerve palsy C1961835 Gaucher disease, type 1 MalaCards C0742291 Chest pain char sharp C0741025 Chest problem UMLS C4084768 Usual severity vomiting C0017601 Glaucomas HSDN C0039070 Collapse fleeting C0600104 Obsessive compulsive behavior HSDN C2024893 Cardiovascular surgery result: fatigue C1864952 Hyperinsulinemic hypoglycemia, familial, 5 MalaCards C0020672 Body temperature decreased C0040053 Thrombosis HSDN C1961131 Cough adverse event C1623041 Breast-fed HSDN C1963063 Anorexia adverse event C3541306 Plasmodium measurement HSDN C0242936 Center pain C0012243 Digestive system neoplasms HSDN C4085211 Pain distress question C0023530 Leukopenia HSDN C2984057 Have nausea C0018800 Cardiomegaly HSDN C3146279 Coma C0342720 Adenosylcobalamin synthesis defect MalaCards C4020887 Photodysphoria C0015624 Fanconi syndrome HPO C4085317 Diarrhea frequency C0878544 Cardiomyopathies HSDN C0033774 Skin pruritus C2984289 Melanoma pathway HSDN C0028738 Nystagmus C1412397 Ancr gene HPO C1279888 Proteinuria of undiagnosed cause C0017638 Glioma HSDN C3887638 Failure to thrive in infant C0001768 Agammaglobulinemia OrphaNet|MalaCards C1963246 Sinus tachycardia adverse event C0031511 Pheochromocytoma MalaCards C4084768 Usual severity vomiting C0001125 Acidosis, lactic HSDN C0039231 Heartbeats increased C3888018 Congenital hyperinsulinism MalaCards C1963281 Vomiting adverse event C0015408 Eye injury HSDN C3665492 Pigmentations C0474824 Halo nevus MalaCards C4085862 Bothered by nausea C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C1963086 Confusion adverse event C0009450 Disease caused by microorganism HSDN C1963180 Neck pain adverse event C0032371 Poliomyelitis HSDN C0011991 Loose stools C0409959 Osteoarthritis, knee HSDN C0003113 Anomia C0376542 Cognitive science HSDN C0278134 Anesthesias C0155084 Neurotrophic keratoconjunctiv. UMLS C0019079 Bloody sputum C0151744 Myocardial ischemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026847 Spinal muscular atrophy HSDN C0013604 Edematous C3714644 Thymus neoplasms OrphaNet|HSDN|MalaCards C4042891 Sleep wake disorders C0016483 Food preferences HSDN C0152459 Striae C0151526 Premature birth HSDN C0004093 Asthenia C0002884 Hypochromic anemia HSDN C1279888 Proteinuria of undiagnosed cause C0268389 Amyloidosis, familial visceral MalaCards|HPO C0009421 Comatose C0520946 Emotional hypersensitivity HSDN C3463815 Feel fatigue C1547940 Specimen source codes - ulcer HSDN C0460137 Push down or depress C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0010520 Skin cyanosis C0004275 Attitude health HSDN C0030193 Sense of pain C1336475 Paranasal sinus cancer stage i UMLS C0039870 Leanness C0700072 Encounter due to stillbirth HSDN C0013421 Dystonia C0009240 Cognition HSDN C4084776 Weight loss C0010823 Cytomegalovirus infections HSDN C1962972 Proteinuria adverse event C0751746 Amino acid transport disorders, inborn HSDN C0019825 Voice hoarseness C1839259 Bulbo-spinal atrophy, x-linked OrphaNet|HPO C0003113 Anomia C0007786 Brain ischemia HSDN C1557397 Adverse event associated with pain C0023051 Laryngeal diseases HSDN C4084774 Have weight loss C0344479 Spinal cord myelodysplasia HSDN C0235031 Neurological complaint C0011206 Delirium UMLS C2024878 Cardiovascular surgery result: dyspnea C0949658 Cardiomyopathy, hypertrophic, familial HSDN C0015938 Fetal macrosomia C0342257 Complications of diabetes mellitus HSDN C0043094 Weight gain C0041408 Turner syndrome HSDN C0043094 Weight gain C0021051 Immunologic deficiency syndromes HSDN C2911645 Weight loss adverse event C0029928 Ovarian diseases HSDN C0085636 Light sensitivity C0043253 Trauma blunt HSDN C0023015 Language handicap C1956346 Coronary artery disease HSDN C0036572 Convulsion C0393684 Cingulate epilepsies UMLS C0162292 Extraocular palsy C3554599 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 MalaCards C0030975 Disorders perception C0028738 Nystagmus HSDN C0013390 Cramps menstrual C0030305 Pancreatitis HSDN C0039070 Collapse fleeting C0038661 Suicide HSDN C0000727 Abdomen acute C0035243 Respiratory tract infections HSDN C0015469 Facial paralysis C0220654 Meningeal carcinomatosis HSDN C0332573 Macula C0855017 Stage iii acral lentiginous melanoma UMLS C3541349 Syncope C1556682 Adverse event associated with infection HSDN C0042963 Symptoms vomiting C0005416 Biliary dyskinesia HSDN C0010200 Cough symptom C0008728 Churg-strauss syndrome MalaCards C0086437 Joint hypermobility C0342853 Sialuria OrphaNet|HPO|MalaCards C3665347 Vision impaired C1842836 Congenital disorder of glycosylation, type ii MalaCards|HPO C0231528 Muscle pain generalized C0242994 Hantavirus infections HSDN C0018681 Headache, cephalalgia C0003467 Anxiety HSDN C1145670 Failure respiratory C0544012 Aberfeld's syndrome MalaCards C0232461 Increased appetite C0040156 Thyrotoxicosis MalaCards C0019079 Bloody sputum C0039981 Thoracic neoplasms HSDN C0518090 Frequency of pain question C0023530 Leukopenia HSDN C0027497 Queasy C0016057 Fibrosarcoma HSDN C4084726 Distress cough C1963198 Pancreatitis adverse event HSDN C0000737 Abdomen pain C0017601 Glaucomas HSDN C0013604 Edematous C0860603 Anxiety symptoms HSDN C0009806 Constipate C0040136 Thyroid neoplasm HSDN C4084767 Bothered by vomiting C1457883 Aggressive reaction HSDN C2919142 Short stature adverse event C0271585 Isolated trh deficiency MalaCards C4085862 Bothered by nausea C0034067 Pulmonary emphysema HSDN C0033377 Caudal displacement C0041408 Turner syndrome MalaCards C0030193 Sense of pain C0024286 Lymphogranuloma venereum HSDN C3829611 Nausea frequency C0005426 Biliary tract neoplasm HSDN C0013404 Respiratory difficulty C0024620 Primary malignant neoplasm of liver MalaCards C0557874 Global developmental delay C2931776 Der kaloustian mcintosh silver syndrome OrphaNet|MalaCards C0162298 Stiffness joints C0814154 Alcohol-related neurodevelopmental disorder OrphaNet|MalaCards C1963091 Diarrhea adverse event C0025303 Meningococcal infections HSDN C0151889 Reflexes tendon increased C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0031911 Pigment deposition C1333749 Gallbladder melanoma MalaCards C1963281 Vomiting adverse event C0006261 Bronchial diseases HSDN C0557874 Global developmental delay C2931482 Neurofibromatosis-noonan syndrome MalaCards|HPO C0014724 Burping C0012746 Dissociative disorder HSDN C2984058 Have pain C0038273 Stereotypic movement disorder HSDN C0575081 Abnormal gait C1839566 Charcot-marie-tooth disease, x-linked recessive, 5 MalaCards|HPO C3274924 Have been coughing C0021841 Intestinal neoplasms HSDN C3887638 Failure to thrive in infant C0008626 Congenital chromosomal disease HSDN C4084769 Vomiting frequency C0085693 Acute appendicitis nos (disorder) MalaCards C3887638 Failure to thrive in infant C0016470 Food allergy HSDN C2919142 Short stature adverse event C3150644 Brachydactyly, type e2 MalaCards|HPO C0000737 Abdomen pain C0023895 Liver diseases HSDN C0518090 Frequency of pain question C0043048 Experimental water deprivation HSDN C4084767 Bothered by vomiting C0003047 Animal disease HSDN C0349588 Stature short C0796099 Cleft lip-palate with abnormal thumbs and microcephaly MalaCards C0007758 Cerebellar ataxia C0004623 Bacterial infections HSDN C3463815 Feel fatigue C0517555 Venous thrombosis after immobility HSDN C0746674 Muscle weakness generalized C3148763 Muscular dystrophy, limb-girdle, type 1e MalaCards C1145670 Failure respiratory C3489726 Geleophysic dysplasia MalaCards C3665386 Abnormal vision C1858806 Cone-rod dystrophy 3 (disorder) MalaCards|HPO C0018989 Paresis of one side of body C1853554 Radiation induced meningioma MalaCards C0011991 Loose stools C0021070 Immunoproliferative disease HSDN C0022346 Yellow skin C1336811 Transplant-related hepatocellular carcinoma UMLS C0004134 Dyssynergia C1859298 Spinocerebellar ataxia, autosomal recessive 2 OrphaNet|HPO|MalaCards C0018524 Hallucinate C0349231 Phobic anxiety disorder HSDN C0007758 Cerebellar ataxia C0032343 Poisoning HSDN C2984058 Have pain C0007279 Carotid body paraganglioma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C3813607 Infantile gastroesophageal reflux HSDN C3898969 Have been vomiting C0033953 Psychosexual disorders HSDN C0221752 Rbc urine C1961835 Gaucher disease, type 1 MalaCards|HPO C0030554 Abnormal sensation C0271865 Autoimmune hypoparathyroidism OrphaNet|MalaCards C0151827 Pain eye C2316212 Cryopyrin-associated periodic syndromes HSDN C0332563 Papulae C0024899 Mastocytosis MalaCards C2029884 Hearing loss by exam C0007137 Squamous cell carcinoma HSDN C0030554 Abnormal sensation C0751955 Brain infarction HSDN C0151686 Growth retardation C0749420 Thyroid agenesis HPO C0015672 Decreased energy C0850803 Anaphylaxis (non medication) HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206620 Lymphangioma, cystic HSDN C2242996 Tingling C0022367 Jaw, edentulous, partially HSDN C4084774 Have weight loss C2936779 Hydroxymethylbilane synthase deficiency MalaCards C3665347 Vision impaired C0265374 Warfarin syndrome MalaCards C0018681 Headache, cephalalgia C3146259 Stage iv nasopharyngeal carcinoma ajcc v7 UMLS C4085211 Pain distress question C0019556 Canine hip dysplasia HSDN C0042940 Disorder of voice C0040517 Gilles de la tourette syndrome HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C2984058 Have pain C0032066 Plague vaccines HSDN C1963091 Diarrhea adverse event C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C3898969 Have been vomiting C0019557 Hip fx HSDN C0013404 Respiratory difficulty C0025427 Mercury poisoning OrphaNet|MalaCards C0000737 Abdomen pain C0233629 Thinking and speaking disturbances HSDN C0242670 Chronic vegetative state C1579931 Depressed - symptom HSDN C0851578 Disorder sleep C0035439 Rheumatic heart disease HSDN C0042963 Symptoms vomiting C0005974 Bone resorption HSDN C1963184 Nystagmus adverse event C3151056 Spastic paraplegia 51, autosomal recessive MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0015726 Focused anxiety HSDN C0751837 Gait ataxic C3542549 Spastic paraplegia 49, autosomal recessive MalaCards|UMLS C1963091 Diarrhea adverse event C0013922 Embolism HSDN C2024893 Cardiovascular surgery result: fatigue C0018802 Congestive heart failure HSDN C4084773 Bothered by weight gain C0035457 Rhinitis, allergic, perennial HSDN C4085210 Usual severity pain C0030807 Pemphigus, nos HSDN C0009806 Constipate C3809454 Hypotonia, infantile, with psychomotor retardation and characteristic facies 1 UMLS C0012569 Double vision C0031117 Peripheral neuropathy HSDN C0012833 Dizzy C0033975 Psychotic disorders HSDN C0557874 Global developmental delay C1838121 Acrocardiofacial syndrome MalaCards C3898969 Have been vomiting C1457883 Aggressive reaction HSDN C1962972 Proteinuria adverse event C1547046 Kind of quantity - taste HSDN C0024032 Birth weight subnormal C2678480 Chromosome 22q11.2 deletion syndrome, distal MalaCards C1549543 Administration method - pain C0025637 Methemoglobinemia HSDN C0038002 Spleen enlargement C0023240 Legionellosis MalaCards C3887638 Failure to thrive in infant C2931277 Pena shokeir syndrome type 2 MalaCards C0000727 Abdomen acute C0001973 Alcoholic intoxication, chronic HSDN C0013404 Respiratory difficulty C0036330 Schistosomiasis mansoni HSDN C0018777 Deafness, conductive C0085094 Head injury closed HSDN C4084769 Vomiting frequency C0032460 Polycystic ovary syndrome HSDN C4085210 Usual severity pain C0038013 Ankylosing spondylitis DiseaseOntology|MalaCards C0022346 Yellow skin C2981635 Stage iiia hilar cholangiocarcinoma UMLS C1963091 Diarrhea adverse event C1264008 Chronic cold agglutinin disease MalaCards C1768507 Yellow nails C1842307 Ectodermal dysplasia, hypohidrotic, with acanthosis nigricans MalaCards C0011991 Loose stools C0036357 Psychology, schizophrenic HSDN C4084768 Usual severity vomiting C1533628 Pseudo-zellweger syndrome MalaCards C0039070 Collapse fleeting C0025281 Meniere disease HSDN C2911645 Weight loss adverse event C0030653 Behavior, paternal HSDN C3829611 Nausea frequency C1090821 Sepsis (invertebrate) HSDN C0406405 Delayed cold sensitivity C0042109 Urticaria UMLS C4085210 Usual severity pain C0003886 Arthrogryposis HSDN C4085661 Usual severity nausea C0333355 Inflammatory disease of mucous membrane HSDN C0019079 Bloody sputum C0042769 Virus diseases HSDN C0007758 Cerebellar ataxia C0270730 Mptp induced parkinsonism HSDN C0036572 Convulsion C4040133 Complex partial epileptic seizure of occipital lobe UMLS C4049644 Depression C2936741 Syndrome xxyy OrphaNet|MalaCards C0151889 Reflexes tendon increased C0035334 Retinitis pigmentosa MalaCards|HPO C0018681 Headache, cephalalgia C3897753 Recurrent childhood giant cell glioblastoma UMLS C0027796 Neuralgias C0039144 Syringomyelia HSDN C0007758 Cerebellar ataxia C0520946 Emotional hypersensitivity HSDN C0019079 Bloody sputum C0013927 Embolism, amniotic fluid HSDN C0042940 Disorder of voice C0040188 Tic disorder HSDN C3898969 Have been vomiting C0006145 Breast diseases HSDN C4084802 Usual severity diarrhea C0011615 Dermatitis, atopic HSDN C0002170 Alopecia disorders C0268680 Biotin deficiency MalaCards C0018991 Paralysis one side of body C0029458 Osteoporosis, postmenopausal HSDN C3641756 Have diarrhea C0043325 Xanthomatosis HSDN C1961131 Cough adverse event C0001828 Agricultural workers' diseases HSDN C1145670 Failure respiratory C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C1549543 Administration method - pain C0016548 Foreign body migration HSDN C1963065 Apnea adverse event C0012979 Canine disease HSDN C3665347 Vision impaired C0268281 Infantile neuronal ceroid lipofuscinosis OrphaNet|MalaCards C0004093 Asthenia C0013720 Ehlers-danlos syndrome HSDN C2024878 Cardiovascular surgery result: dyspnea C0023343 Leprosy HSDN C2024893 Cardiovascular surgery result: fatigue C2984291 Glioblastoma multiforme pathway HSDN C0042023 Urination frequency C0600040 Chronic interstitial cystitis OrphaNet C0012833 Dizzy C0017178 Gastrointestinal diseases HSDN C0023015 Language handicap C0751955 Brain infarction HSDN C0007758 Cerebellar ataxia C0398794 Hypopigmentation-immunodeficiency disease MalaCards C0013604 Edematous C1963274 Vasculitis adverse event HSDN C1963091 Diarrhea adverse event C0086543 Cataract nos HSDN C1963071 Back pain adverse event C0206732 Epithelioid hemangioendothelioma HSDN C4084766 Vomiting C0034929 Reflex HSDN C0036572 Convulsion C0026267 Mitral valve prolapse syndrome HSDN C0557874 Global developmental delay C3553661 Cerebellar ataxia, nonprogressive, with mental retardation MalaCards C0085636 Light sensitivity C0036202 Sarcoidosis MalaCards C1384666 Decreased hearing C0796117 Pitt syndrome MalaCards C0020455 Hypergammaglobulinemia C0003509 Aortitis, nos HSDN C1963180 Neck pain adverse event C0001828 Agricultural workers' diseases HSDN C3539023 Pelvic pain increasing in frequency C0010692 Cystitis HSDN C0221263 Cafe au lait spot C1969056 Leopard syndrome 2 MalaCards|HPO C4084768 Usual severity vomiting C0037937 Spine injury HSDN C1549543 Administration method - pain C0030499 Parasitic diseases HSDN C0242936 Center pain C0015300 Exophthalmos HSDN C0013404 Respiratory difficulty C0022821 Kyphosis deformity of spine HSDN C4085210 Usual severity pain C0030567 Parkinson disease HSDN C0015672 Decreased energy C0029928 Ovarian diseases HSDN C2984058 Have pain C0013595 Eczema HSDN C0020673 Hypothermia (central) (local) C0040046 Thrombophlebitis HSDN C0232466 Feeding difficulty C0393706 Early infantile epileptic encephalopathy with suppression bursts MalaCards C0037384 Snore C0009404 Colorectal neoplasms HSDN C0002622 Amnesias C0014832 Escape reaction HSDN C1963066 Joint pain adverse event C0524910 Hepatitis c, chronic MalaCards C1963091 Diarrhea adverse event C0042018 Urinary calculi HSDN C0221263 Cafe au lait spot C1854465 Tuberous sclerosis 1 (disorder) HPO C0002962 Angina C0015671 Father HSDN C4085317 Diarrhea frequency C2745948 Hyalinosis, systemic MalaCards C1319542 On examination - left eye proliferative diabetic retinopathy C1532588 Diabetic retinopathy proliferative left eye, stable treated UMLS C1961131 Cough adverse event C0007873 Uterine cervical neoplasm HSDN C0016204 Fart C0011581 Depressive disorder HSDN C2315100 Pediatric failure to thrive C2748608 Lead poisoning, susceptibility to HPO C0231528 Muscle pain generalized C0003490 Aortic arch syndrome MalaCards C0013604 Edematous C0155843 Retropharyngeal abscess HSDN C0036572 Convulsion C3899649 Childhood oligoastrocytoma UMLS C0039870 Leanness C0014175 Endometriosis HSDN C0007758 Cerebellar ataxia C1969562 Mental retardation, autosomal dominant 1 HPO C4085661 Usual severity nausea C0011884 Diabetic retinopathy HSDN C1963180 Neck pain adverse event C0023676 Life style HSDN C0851578 Disorder sleep C0020517 Hypersensitivity HSDN C4084774 Have weight loss C0029456 Osteoporosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0085183 Neoplasms, second primary HSDN C1961131 Cough adverse event C1962979 Burn adverse event HSDN C0009421 Comatose C0002792 Anaphylaxis HSDN C0424755 Fever symptoms C0029440 Osteoma HSDN C0012569 Double vision C0752235 Lyme neuroborreliosis HSDN C0033377 Caudal displacement C1845146 Holoprosencephaly, ectrodactyly, and bilateral cleft lip-palate OrphaNet|HPO|MalaCards C2919142 Short stature adverse event C0796264 Young-hughes syndrome OrphaNet|MalaCards C4084802 Usual severity diarrhea C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0424755 Fever symptoms C0037299 Skin ulcer HSDN C4084768 Usual severity vomiting C3536715 Aa amyloidosis MalaCards C0015672 Decreased energy C0027831 Neurofibromatosis 1 HSDN C0036659 Sensation disorder C0015726 Focused anxiety HSDN C1963086 Confusion adverse event C0017601 Glaucomas HSDN C2911645 Weight loss adverse event C0037928 Spinal cord diseases HSDN C2984058 Have pain C0009376 Colonic polyps HSDN C0151786 Weakness muscle C0017531 Angiolymphoid hyperplasia HSDN C0005745 Blepharoptosis C2931196 Craniofacial dysostosis type 1 MalaCards C0042963 Symptoms vomiting C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency HPO C0013911 Emaciate C0003962 Ascites HSDN C3539893 Pelvic pain occurs with intercourse C0042996 Vulvitis unspecified HSDN C0033774 Skin pruritus C0002878 Anemia, hemolytic HSDN C0013404 Respiratory difficulty C0005424 Biliary tract diseases HSDN C4085211 Pain distress question C0027126 Myotonic dystrophy HSDN C0018681 Headache, cephalalgia C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0016199 Pain flank C0206635 Myelolipoma HSDN C0497247 Blood pressure elevation C1857563 Hsd11b2, tyr299del HPO C0015672 Decreased energy C0043168 Whooping cough due to unspecified organism HSDN C2242996 Tingling C0005586 Bipolar disorder HSDN C0037317 Sleep disturbance C4048800 Telomeric 22q13 monosomy syndrome MalaCards C0007758 Cerebellar ataxia C0035204 Respiration disorders HSDN C1959630 Eye pain adverse event C0003081 Anisometropia HSDN C0018808 Murmur C0027051 Myocardial infarction HSDN C0019521 Hiccoughs C4084909 Depression subordinate domain HSDN C2024893 Cardiovascular surgery result: fatigue C1858592 Carney triad OrphaNet|MalaCards C4084784 Diarrhea C0524910 Hepatitis c, chronic HSDN C0018681 Headache, cephalalgia C0039336 Gustatory sense HSDN C0268988 Itch penis C0459151 Disorder of soft tissue of trunk UMLS C0023015 Language handicap C0460137 Push down or depress HSDN C0013404 Respiratory difficulty C0023801 Lipomatosis HSDN C0751401 Ophthalmoparesis C1956390 Cranial arteritis MalaCards C1962972 Proteinuria adverse event C2674045 Urogenital adysplasia HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0680727 Mediation HSDN C1971624 Appetite absent C4049994 Insulin resistance measurement HSDN C0033377 Caudal displacement C0796184 Corpus callosum, agenesis of, with facial anomalies and robin sequence MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C1963120 Gynecomastia adverse event HSDN C0028961 Urine output decreased C0343084 Capillary leak syndrome HSDN C4085210 Usual severity pain C2717865 Anti-neutrophil cytoplasmic antibody-associated vasculitis HSDN C4049644 Depression C2930798 Alexanders leukodystrophy MalaCards C2911645 Weight loss adverse event C3541306 Plasmodium measurement HSDN C0424755 Fever symptoms C2979888 Fever, australian q MalaCards C0015970 Fever unknown origin C2073625 X-ray of chest: pleural effusion HSDN C0349588 Stature short C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C1963184 Nystagmus adverse event C1412747 Bbs2 gene HPO C2984057 Have nausea C0003467 Anxiety HSDN C0026826 High muscle tone C2931646 Oculocerebral hypopigmentation syndrome type preus OrphaNet|MalaCards C1963281 Vomiting adverse event C0036946 Sheep--diseases HSDN C1963184 Nystagmus adverse event C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C0024437 Macular degeneration HSDN C0235980 Scleral discoloration C0023931 Lobstein's disease UMLS C0002963 Angina variant C0004245 Atrioventricular block HSDN C0037317 Sleep disturbance C1863959 Hyperthyroidism, familial gestational OrphaNet|HPO|MalaCards C4084727 Cough frequency C0027092 Myopia HSDN C4061656 Increase in perspiration C0003467 Anxiety UMLS C0025287 Meningitis-like C0037886 Sinusitis sphenoid HSDN C0009806 Constipate C0460137 Push down or depress HSDN C0518090 Frequency of pain question C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C0023012 Delay language C1859817 2-aminoadipic 2-oxoadipic aciduria HPO C0036659 Sensation disorder C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4084788 Have dizziness C1690964 Cataract HSDN C0015230 Exanthem C0477524 Other granulomatous disorders of the skin and subcutaneous tissue UMLS C0015469 Facial paralysis C0432272 Van buchem disease OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0009324 Ulcerative colitis HSDN C0013604 Edematous C0037116 Silicosis HSDN C0413252 Hypothermia due to exposure C0023364 Leptospirosis HSDN C0011991 Loose stools C3146297 Study of behavior during childhood HSDN C4084784 Diarrhea C0018081 Gonorrhea HSDN C0751354 Action myoclonus C3279627 Epilepsy, progressive myoclonic, 6 UMLS C1279888 Proteinuria of undiagnosed cause C0009240 Cognition HSDN C0030193 Sense of pain C0003496 Aortic rupture HSDN C4084725 Usual severity cough C3179093 Injuries, laryngeal nerve HSDN C0030193 Sense of pain C0030756 Pediculosis HSDN C4085210 Usual severity pain C0008519 Ectopic tissue HSDN C0042963 Symptoms vomiting C0025637 Methemoglobinemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1691215 Penile hypospadias HSDN C2984057 Have nausea C0028738 Nystagmus HSDN C0010200 Cough symptom C0024117 Chronic obstructive airway disease UMLS C0917816 Deficiency mental C0265339 Borjeson-forssman-lehmann syndrome OrphaNet|HPO|MalaCards C0019079 Bloody sputum C0007873 Uterine cervical neoplasm HSDN C2984058 Have pain C1000587 Pemphigus HSDN C3641756 Have diarrhea C0029295 Oropharyngeal neoplasms HSDN C0011168 Disorder deglutition C1853247 Spastic paraplegia 31, autosomal dominant MalaCards|HPO C1549543 Administration method - pain C0001618 Tumors of adrenal cortex HSDN C4084723 Constipation C0022658 Kidney diseases HSDN C0027497 Queasy C0000768 Congenital abnormality HSDN C0042963 Symptoms vomiting C0018824 Heart valve disease HSDN C0015469 Facial paralysis C0038013 Ankylosing spondylitis HSDN C0036396 Sciatica C0037369 Smoking HSDN C0023015 Language handicap C0026650 Movement disorders HSDN C3146279 Coma C0036323 Schistosomiasis HSDN C1963064 Anxiety adverse event C1868681 Dystonia 12 HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0013369 Dysentery HSDN C1963170 Hypothermia adverse event C0035435 Rheumatism HSDN C2237041 Shox gene with short stature C0025237 Melnick-needles syndrome MalaCards C0023380 Lethargy C2937225 Biotin deficiency disease MalaCards C1557397 Adverse event associated with pain C0017661 Iga glomerulonephritis HSDN C3146279 Coma C0023467 Leukemia, myelocytic, acute HSDN C3887873 Hearing loss C0043251 Wounds and injuries HSDN C1549543 Administration method - pain C0033871 Psychiatric status rating scales HSDN C2315100 Pediatric failure to thrive C0268542 Ornithine carbamoyltransferase deficiency HPO C2919142 Short stature adverse event C1842465 Lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones OrphaNet|MalaCards C1963137 Hydrocephalus adverse event C2675891 Chromosome 1q21.1 duplication syndrome MalaCards C3887784 Decreased urine output C0019101 Hemorrhagic fever with renal syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C0001957 Alcohol withdrawal delirium HSDN C4084724 Usual severity constipation C3809877 Schaaf-yang syndrome MalaCards C4085211 Pain distress question C1705812 Nci thesaurus role HSDN C0085610 Bradycardia sinus C1970119 Cardiac arrhythmia, ankyrin-b-related MalaCards|HPO C1963065 Apnea adverse event C0432240 Stuve-wiedemann dysplasia OrphaNet|HPO C0018772 Deafness C1546602 Specimen source codes - diverticulum HSDN C1279888 Proteinuria of undiagnosed cause C0027659 Neoplasms, experimental HSDN C1962972 Proteinuria adverse event C0007781 Intracranial embolism and thrombosis HSDN C4084766 Vomiting C0017638 Glioma HSDN C3641756 Have diarrhea C0221056 Adult type dermatomyositis HSDN C3641756 Have diarrhea C0022890 Labyrinthine disorder HSDN C2024893 Cardiovascular surgery result: fatigue C0001883 Airway obstruction HSDN C0009421 Comatose C0038819 Siriasis HSDN C0041657 Consciousness loss C0019337 Heroin dependence HSDN C0043094 Weight gain C0024117 Chronic obstructive airway disease HSDN C0035078 Failure kidney C2939174 Medullary cystic disease MalaCards C0040264 Ear ringing sound C0030567 Parkinson disease HSDN C2984058 Have pain C0680727 Mediation HSDN C0020796 Profoundly mentally retarded C3280856 Ichthyosis, spastic quadriplegia, and mental retardation MalaCards C0233514 Behavior abnormal C0175701 Aarskog syndrome MalaCards C0751837 Gait ataxic C0243010 Viral encephalitis HSDN C2237041 Shox gene with short stature C3151433 Osteogenesis imperfecta, type xii MalaCards C4084773 Bothered by weight gain C3536741 Discordant ventriculoarterial connection HSDN C4084769 Vomiting frequency C0080178 Spina bifida HSDN C1279888 Proteinuria of undiagnosed cause C3463824 Myelodysplastic syndrome HSDN C2024893 Cardiovascular surgery result: fatigue C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C4084768 Usual severity vomiting C0524851 Neurodegenerative disorders HSDN C4085211 Pain distress question C0015302 External exotoses HSDN C0497247 Blood pressure elevation C3151268 Lipodystrophy, familial partial, type 4 MalaCards|HPO C4084723 Constipation C0346407 Pancreatic polypeptide-oma MalaCards C4084802 Usual severity diarrhea C0086649 Mps iii c HPO C4084774 Have weight loss C0868910 Oligozoospermia HSDN C0018784 Deafness sensorineural C1969652 Brachydactyly, type b2 (disorder) MalaCards|HPO C0518090 Frequency of pain question C0424688 Small head HSDN C4084769 Vomiting frequency C0018790 Cardiac arrest HSDN C4085211 Pain distress question C0036239 Satiety HSDN C0040264 Ear ringing sound C0026764 Multiple myeloma HSDN C0026826 High muscle tone C0010692 Cystitis HSDN C3146279 Coma C0020517 Hypersensitivity HSDN C0027497 Queasy C0003175 Anthrax disease MalaCards C4084802 Usual severity diarrhea C0238386 Cronkhite-canada disease MalaCards C3539891 Pelvic pain to the rear C0314657 Genetic predisposition HSDN C1963091 Diarrhea adverse event C0024232 Lymphatic metastasis HSDN C3541349 Syncope C0037369 Smoking HSDN C4085862 Bothered by nausea C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C0018772 Deafness C0013182 Drug allergy HSDN C3463815 Feel fatigue C0042111 Urticaria pigmentosa MalaCards C0851578 Disorder sleep C0035372 Rett syndrome HSDN C0036396 Sciatica C0007873 Uterine cervical neoplasm HSDN C0003467 Angst C0031485 Phenylketonurias MalaCards C4084774 Have weight loss C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C1549543 Administration method - pain C0028768 Obsessive-compulsive disorder HSDN C0030193 Sense of pain C0399352 Developmental absence of tooth HSDN C0000737 Abdomen pain C1857728 Hereditary angioedema type iii HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1552052 Religious affiliation - meditation HSDN C4085661 Usual severity nausea C0020517 Hypersensitivity HSDN C0011991 Loose stools C0473133 Protracted diarrhea UMLS C2029884 Hearing loss by exam C3850155 Congenital microtia HSDN C0233514 Behavior abnormal C1839564 Jensen syndrome MalaCards C0018784 Deafness sensorineural C1864968 Deafness, autosomal recessive 51 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0004245 Atrioventricular block HSDN C2024878 Cardiovascular surgery result: dyspnea C0004031 Aspergillosis, allergic bronchopulmonary HSDN C0030552 Paralysis partial C2239176 Liver carcinoma HSDN C1971624 Appetite absent C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C4084769 Vomiting frequency C0031046 Pericarditis HSDN C3641756 Have diarrhea C0282687 Hemorrhagic fever, ebola DiseaseOntology|OrphaNet|MalaCards C0013604 Edematous C0021432 Infratentorial neoplasms HSDN C0424755 Fever symptoms C1282908 De vaal's syndrome OrphaNet|HPO|MalaCards C0231835 Respiration rate increased C1857780 Joubert syndrome 5 MalaCards C0006370 Bulimia C0040435 Tooth diseases HSDN C0035078 Failure kidney C0162565 Acute intermittent porphyria MalaCards|HPO C0009806 Constipate C0001175 Acquired immunodeficiency syndrome HSDN C1963077 Bone pain adverse event C1839874 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis OrphaNet C4084727 Cough frequency C0032966 Complication, neoplastic pregnancy HSDN C0013604 Edematous C0026266 Mitral valve insufficiency HSDN C0018524 Hallucinate C0017178 Gastrointestinal diseases HSDN C0036572 Convulsion C0339289 Injury corneal HSDN C0013421 Dystonia C0587248 Costello syndrome (disorder) HSDN C4085211 Pain distress question C2267227 Bulimia nervosa HSDN C0012569 Double vision C0024904 Mastoiditis HSDN C0241165 Skin thickening C0392784 Dermatofibrosarcoma protuberans OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0175702 Williams syndrome OrphaNet|HSDN|HPO|MalaCards C0018926 Emesis bloody C0008625 Chromosome aberrations HSDN C0013421 Dystonia C0024121 Lung neoplasms HSDN C0086437 Joint hypermobility C0917715 Hajdu-cheney syndrome MalaCards|HPO|UMLS C0151889 Reflexes tendon increased C2678416 Hyperphenylalaninemia, non-pku mild HPO C0036572 Convulsion C2674937 Chromosome 10q26 deletion syndrome MalaCards|UMLS C2315100 Pediatric failure to thrive C0268573 Valinemia MalaCards C0917816 Deficiency mental C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards C0024032 Birth weight subnormal C1135161 Stage 4s neuroblastoma MalaCards C0042963 Symptoms vomiting C0033975 Psychotic disorders HSDN C3163620 Hypotension adverse event C3810282 Chromosome 5q12 deletion syndrome MalaCards C0041105 Jaw spasm C0037369 Smoking HSDN C0026838 Spasticity muscle C0751918 Cockayne pelizaeus merzbacher disease MalaCards C2315100 Pediatric failure to thrive C0221032 Familial generalized lipodystrophy HSDN C0043094 Weight gain C0282507 Heat stress disorders HSDN C0033774 Skin pruritus C0005586 Bipolar disorder HSDN C0340288 Angina stable C0011875 Diabetic angiopathies HSDN C0151786 Weakness muscle C0751587 Cadasil syndrome HSDN C2919142 Short stature adverse event C0008626 Congenital chromosomal disease MalaCards C0009806 Constipate C0004352 Autistic disorder HSDN C0002622 Amnesias C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C1963091 Diarrhea adverse event C0016057 Fibrosarcoma HSDN C0917816 Deficiency mental C1846388 Cortical dysplasia of taylor, dysplasia only HPO C1260880 Nasal drip C1333474 Ethmoid sinus inverted papilloma UMLS C0013428 Painful urination C0042170 Uveomeningoencephalitic syndrome HSDN C0917816 Deficiency mental C1855606 Burton syndrome MalaCards C4085661 Usual severity nausea C0043124 West nile fever MalaCards C0085636 Light sensitivity C3150912 Cone-rod dystrophy 15 MalaCards|HPO C0036572 Convulsion C0149778 Soft tissue infections HSDN C1959630 Eye pain adverse event C0031024 Suppurative periapical periodontitis HSDN C0575081 Abnormal gait C0795889 Allan-herndon-dudley syndrome (ahds) OrphaNet C1856661 Cornea cloudy C0544008 Chandler syndrome MalaCards C0011991 Loose stools C0040954 Infection by trichuris trichiura DiseaseOntology|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0019154 Hepatic vein thrombosis HSDN C0012833 Dizzy C0751815 Carotid artery, internal, dissection HSDN C1963093 Dizziness adverse event C0030286 Pancreatic diseases HSDN C0018681 Headache, cephalalgia C1556682 Adverse event associated with infection HSDN C0007758 Cerebellar ataxia C1839780 Fragile x tremor/ataxia syndrome OrphaNet|MalaCards C3463815 Feel fatigue C4049994 Insulin resistance measurement HSDN C0036396 Sciatica C0812393 Cancer patients and suicide and depression HSDN C0349588 Stature short C1840334 Hypoparathyroidism, autosomal recessive MalaCards C0018681 Headache, cephalalgia C0041956 Ureteral obstruction HSDN C0151889 Reflexes tendon increased C0015625 Fanconi anemia MalaCards|HPO C1260880 Nasal drip C0021400 Influenza DiseaseOntology|MalaCards C3641755 Have constipation C0878683 Pituitary dwarfism type 3 MalaCards C0027497 Queasy C0033968 Psychotherapeutic technique HSDN C0007758 Cerebellar ataxia C2673874 Bardet biedl syndrome 14 (disorder) HPO C0023012 Delay language C0796250 Partington x-linked mental retardation syndrome HPO C0000731 Abdomen distention C0342200 Endemic cretinism MalaCards C0039070 Collapse fleeting C0013990 Pathological accumulation of air in tissues HSDN C4085548 Usual severity dizziness C0008066 Child behavior disorders HSDN C1519353 Skin eruption papular C1839988 Ichthyosis follicularis atrichia photophobia syndrome MalaCards C4084725 Usual severity cough C2973787 Coxiella burnetii infection MalaCards C3898969 Have been vomiting C0162565 Acute intermittent porphyria MalaCards|HSDN|HPO C4085210 Usual severity pain C0031046 Pericarditis HSDN C0023012 Delay language C3806402 Epilepsy, focal, with speech disorder and with or without mental retardation MalaCards C3829611 Nausea frequency C0042076 Urologic neoplasms HSDN C1549543 Administration method - pain C0085409 Polyendocrinopathies, autoimmune HSDN C0039070 Collapse fleeting C0343084 Capillary leak syndrome HSDN C4042891 Sleep wake disorders C0042769 Virus diseases HSDN C0151827 Pain eye C0517555 Venous thrombosis after immobility HSDN C0027796 Neuralgias C0005695 Bladder neoplasm HSDN C0002962 Angina C0036421 Systemic scleroderma MalaCards|HSDN C2315100 Pediatric failure to thrive C0549567 Pigmentation disorders HSDN C1263846 Attention deficit disorder with hyperactivity C3180937 15q11.2 microdeletion MalaCards C0085642 Asphyxia reticularis C0005779 Blood coagulation disorders HSDN C0030794 Pelvis pain C1519912 Vaginal adenoid cystic carcinoma UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0043253 Trauma blunt HSDN C0030193 Sense of pain C0340289 Angina new onset UMLS C0010038 Corneal opacity disorder C0021171 Bloch sulzberger syndrome OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0002957 Anger HSDN C0031911 Pigment deposition C1377843 Periosteal osteosarcoma MalaCards C0151889 Reflexes tendon increased C2931010 Congenital disorder of glycosylation type 2e MalaCards C0026826 High muscle tone C0268569 Intermittent maple syrup urine disease HPO C1971624 Appetite absent C0042076 Urologic neoplasms HSDN C3539895 Pelvic pain occurs with bowel movement C0033578 Prostatic neoplasms HSDN C0151786 Weakness muscle C0027663 Neoplasms, multiple primary HSDN C0700078 Deep tendon reflex decrease C3554398 Spinal muscular atrophy, jokela type MalaCards C0034150 Skin purpura C0949683 Sex chromosome disorders HSDN C0578052 Pain of digestive structure C0267515 Chronic idiopathic anal pain UMLS C0018681 Headache, cephalalgia C1332308 Anterior optic tract meningioma UMLS C0424755 Fever symptoms C0878544 Cardiomyopathies HSDN C0038002 Spleen enlargement C2751643 Glycogen storage disease ixc MalaCards|HPO C4084776 Weight loss C0043048 Experimental water deprivation HSDN C0037771 Paraparesis spastic C0220754 Biotinidase deficiency HSDN C2024893 Cardiovascular surgery result: fatigue C0006035 Borrelia infections MalaCards C3146279 Coma C0475072 Traumatic cerebral hemorrhage HSDN C0020505 Excessive eating C0949313 Determinism, genetic HSDN C0040822 D tremors C0549567 Pigmentation disorders HSDN C0232726 Tenesmus, rectal C1335686 Neuroendocrine neoplasm of rectum MalaCards C0028961 Urine output decreased C0041364 Tumor lysis syndrome HSDN C0036572 Convulsion C0153066 Murray valley encephalitis DiseaseOntology|MalaCards C0007166 Cardiac output decreased C0034072 Cor pulmonale HSDN C0751837 Gait ataxic C0751739 Basal ganglia cerebrovascular disease HSDN C0031911 Pigment deposition C1335398 Gastric peutz-jeghers polyp MalaCards C0024032 Birth weight subnormal C3150675 Chromosome 15q24 duplication syndrome HPO C0013404 Respiratory difficulty C0007138 Carcinoma, transitional cell HSDN C0020580 Decreased sensation C0162569 Hepatoerythropoietic porphyria HSDN C0011991 Loose stools C0149678 Epstein-barr virus infections HSDN C3829611 Nausea frequency C0011603 Dermatitis HSDN C0162298 Stiffness joints C1861401 Symphalangism, distal MalaCards C0027497 Queasy C0008370 Cholestasis HSDN C0003469 Anxiety disorder C1864871 Chromosome 17q21.31 deletion syndrome MalaCards C4084767 Bothered by vomiting C0033968 Psychotherapeutic technique HSDN C2032395 Pelvic pain on the left C0026769 Multiple sclerosis HSDN C1557397 Adverse event associated with pain C0037275 Skin diseases, vesiculobullous HSDN C0013604 Edematous C0001427 Adenoiditis, nos MalaCards C0238656 Pain ankle C0221204 Lytic lesion MalaCards C0036572 Convulsion C0029132 Disorder of the optic nerve HSDN C0020673 Hypothermia (central) (local) C0042029 Urinary tract infection HSDN C0020672 Body temperature decreased C0020659 Hypothalamic neoplasms HSDN C0040822 D tremors C1832884 Hemiplegic migraine, familial type 1 MalaCards|HPO C2911645 Weight loss adverse event C0242216 Biliary calculi HSDN C0042963 Symptoms vomiting C1855371 Maple syrup urine disease, type ii HPO C0035229 Respiratory function impaired C0035436 Rheumatic fever MalaCards C2919142 Short stature adverse event C1851841 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 1 HPO C0917816 Deficiency mental C2675891 Chromosome 1q21.1 duplication syndrome OrphaNet|MalaCards C1279888 Proteinuria of undiagnosed cause C0009324 Ulcerative colitis HSDN C0042571 Vertigo subjective C0020701 Somatization disorder HSDN C0522224 Palsied C0007959 Charcot-marie-tooth disease OrphaNet|MalaCards C3898969 Have been vomiting C2931618 Gestational trophoblastic disease HSDN C0268988 Itch penis C1290026 Disease of skin and/or subcutaneous tissue of trunk UMLS C3541349 Syncope C0037650 Somatoform disorder HSDN C0030200 Intractable pain C2984299 Asthma pathway HSDN C0042024 Urine incontinence C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C4042891 Sleep wake disorders C0023676 Life style HSDN C3887873 Hearing loss C0039131 Syphilis congenital HSDN C2237041 Shox gene with short stature C1846059 Roifman syndrome MalaCards C0007642 Cellulitis nos C0001768 Agammaglobulinemia MalaCards C4084802 Usual severity diarrhea C0005891 Bodies image HSDN C0030193 Sense of pain C1377785 Nasal cavity carcinoma UMLS C1963091 Diarrhea adverse event C1963083 Cholecystitis adverse event HSDN C0012569 Double vision C0812393 Cancer patients and suicide and depression HSDN C0042024 Urine incontinence C0014544 Epilepsy HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0021295 Infant, premature, diseases HSDN C1963091 Diarrhea adverse event C0019154 Hepatic vein thrombosis HSDN C0013404 Respiratory difficulty C0039730 Thalassemia HSDN C2073625 X-ray of chest: pleural effusion C2930957 Hantavirosis OrphaNet|MalaCards C0221232 Welts C0263335 Traumatic urticaria UMLS C1971624 Appetite absent C1962986 Glaucoma adverse event HSDN C0235267 Eye redness C0009765 Conjunctivitis, acute hemorrhagic DiseaseOntology|MalaCards C0036659 Sensation disorder C1861329 Spinal canal stenosis HSDN C3887638 Failure to thrive in infant C0079153 Hyperkeratosis, epidermolytic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1527348 Brain hypoxia HSDN C0018808 Murmur C0024115 Lung diseases HSDN C4084769 Vomiting frequency C0023055 Laryngeal neoplasm HSDN C0151786 Weakness muscle C0206667 Adrenal cortical adenoma MalaCards C0000727 Abdomen acute C0018802 Congestive heart failure HSDN C3641756 Have diarrhea C0029400 Osteitis HSDN C0042963 Symptoms vomiting C0237873 Physiological sexual disorders HSDN C0000737 Abdomen pain C0006277 Bronchitis UMLS C3898969 Have been vomiting C1963266 Uveitis adverse event HSDN C2911645 Weight loss adverse event C1962958 Hematoma adverse event HSDN C0242936 Center pain C0039981 Thoracic neoplasms HSDN C3539891 Pelvic pain to the rear C0009375 Colonic neoplasms HSDN C0557874 Global developmental delay C1844935 Arthrogryposis, ectodermal dysplasia, cleft lip-palate, and developmental delay OrphaNet|MalaCards C0277799 Fever intermittent C0268293 Corticosterone methyl oxidase type i deficiency HPO C4084784 Diarrhea C0005586 Bipolar disorder HSDN C0030794 Pelvis pain C0227791 Discharge vaginal HSDN C0013404 Respiratory difficulty C0085404 Poems syndrome HSDN C2984058 Have pain C0477611 Spin osteochondrosis, unsp HSDN C0018777 Deafness, conductive C1844680 Deafness-hypogonadism syndrome OrphaNet|MalaCards C0030552 Paralysis partial C0027627 Neoplasm metastasis HSDN C0234146 Absent reflex C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C3665492 Pigmentations C3151228 Retinitis pigmentosa 38 (disorder) MalaCards C1549543 Administration method - pain C0008073 Developmental disabilities HSDN C0000727 Abdomen acute C0027746 Nerve degeneration HSDN C0000737 Abdomen pain C0854788 Recurrent small bowel cancer UMLS C0035078 Failure kidney C0265234 Branchio-oto-renal syndrome MalaCards|HPO C0004134 Dyssynergia C0013182 Drug allergy HSDN C0027796 Neuralgias C0018621 Hay fever HSDN C3163620 Hypotension adverse event C0155866 Inhalational anthrax OrphaNet|MalaCards C4085317 Diarrhea frequency C0011974 Diaper rash HSDN C0020672 Body temperature decreased C0749420 Thyroid agenesis HPO C0162834 Hyperpigmentation C0796070 Microphthalmia, syndromic 7 MalaCards C1962972 Proteinuria adverse event C0018571 Hand injury HSDN C0013528 Echo speech C0037397 Behavior social HSDN C4085862 Bothered by nausea C0018273 Growth disorders HSDN C0242936 Center pain C0424688 Small head HSDN C3829611 Nausea frequency C0042373 Vascular diseases HSDN C1549543 Administration method - pain C0018889 Helminthiasis HSDN C3898969 Have been vomiting C0017638 Glioma HSDN C1963067 Atrial fibrillation adverse event C1832680 Cardiomyopathy, dilated, 1e MalaCards|HPO C0473240 Dipstix hematuria C0042075 Urologic diseases UMLS C4084769 Vomiting frequency C1859499 3-methylcrotonyl coa carboxylase 2 deficiency MalaCards C0022346 Yellow skin C0005967 Bone neoplasms HSDN C0000786 Abortion spontaneous C0001733 Afibrinogenemia MalaCards C4084767 Bothered by vomiting C0004943 Behcet syndrome HSDN C0018681 Headache, cephalalgia C3897750 Recurrent childhood gliosarcoma UMLS C0349588 Stature short C1856198 Hall riggs mental retardation syndrome OrphaNet|MalaCards C0040822 D tremors C3164344 Adult onset autosomal dominant leukodystrophy OrphaNet|HPO C4085222 Nausea C3839212 Familial hyperaldosteronism type 2 MalaCards C4084766 Vomiting C0039494 Temporomandibular joint disorders HSDN C4084724 Usual severity constipation C1848805 Thyroid dyshormonogenesis 1 MalaCards|HPO C0700590 Diaphoresis excessive C0751552 Malignant neoplasm of thymus MalaCards C0003862 Pain joint C1704375 Hypophosphatemic rickets HSDN C0241137 Skin pallor C0271972 Thiamine-responsive megaloblastic anemia MalaCards C0004093 Asthenia C2350015 Data type -character HSDN C0039070 Collapse fleeting C0020461 Hyperkalemia HSDN C2237041 Shox gene with short stature C1855057 Ataxia-telangiectasia variant v2 HPO C0424853 Finger mass C0684458 Secondary malignant skin neoplasm of finger UMLS C0027066 Myoclonic jerking C0009946 Conversion disorder HSDN C3898969 Have been vomiting C0008354 Cholera HSDN C0018784 Deafness sensorineural C0005967 Bone neoplasms HSDN C0015468 Face pain C0002736 Amyotrophic lateral sclerosis HSDN C0019209 Large liver C0342749 Glycogen storage disease ic MalaCards|HPO C4084769 Vomiting frequency C0740392 Infarction, middle cerebral artery HSDN C4049644 Depression C0334123 Histiocytosis, lipoid MalaCards C1963071 Back pain adverse event C0036864 Sexual relations HSDN C0004604 Pain back C0031117 Peripheral neuropathy HSDN C0041657 Consciousness loss C1546847 Entity name part type - family HSDN C1963071 Back pain adverse event C0021843 Intestinal obstruction HSDN C0015230 Exanthem C0342731 Deficiency of mevalonate kinase MalaCards C0018681 Headache, cephalalgia C0206725 Subependymal glioma UMLS C0001825 Agraphia C0017510 Gestures HSDN C1963087 Constipation adverse event C0238198 Gastrointestinal stromal tumors OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0038012 Spondylitis HSDN C3665347 Vision impaired C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0079772 T-cell lymphoma HSDN C1963281 Vomiting adverse event C0752165 Angioma, venous, central nervous system HSDN C1963071 Back pain adverse event C0018021 Goiter HSDN C2984058 Have pain C1527348 Brain hypoxia HSDN C1069915 Vertigo C0027051 Myocardial infarction HSDN C1565249 Limitation, mobility C0344315 Depressed mood HSDN C2132198 Abnormal blistering of the skin C0406707 Basan syndrome OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0030354 Papilloma HSDN C1963071 Back pain adverse event C0553580 Ewings sarcoma HSDN C3539891 Pelvic pain to the rear C0023890 Liver cirrhosis HSDN C4085211 Pain distress question C2350529 Pulmonary aspergillosis HSDN C3815497 Cough C0585442 Osteosarcoma of bone HSDN C0027497 Queasy C0001807 Aggressive behavior HSDN C3641756 Have diarrhea C0242966 Systemic inflammatory response syndrome HSDN C4084766 Vomiting C0035066 Renal artery obstruction HSDN C0030552 Paralysis partial C1864851 Pigmented nodular adrenocortical disease, primary, 2 MalaCards C0037763 Spasm C0006663 Calcinosis HSDN C0518090 Frequency of pain question C0155862 Streptococcal pneumonia HSDN C1279888 Proteinuria of undiagnosed cause C1268935 Congenital thrombotic thrombocytopenic purpura MalaCards|HPO C0018524 Hallucinate C1963083 Cholecystitis adverse event HSDN C2203646 Jaundice C0032787 Postoperative complications HSDN C0270795 Monopareses C0856328 Right arm paresis UMLS C4084767 Bothered by vomiting C0017601 Glaucomas HSDN C4084724 Usual severity constipation C3244301 Coverage level - family HSDN C0018784 Deafness sensorineural C0042373 Vascular diseases HSDN C0869084 Difficulty in walking, not elsewhere classified in icd10cm C0154725 Oth disorder nervous system UMLS C0277959 Hair coarseness C1851841 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 1 OrphaNet|HPO C0008031 Pain chest C2240374 Eosinophil count raised HSDN C0026821 Cramp C1412297 Aic gene HSDN C0013604 Edematous C0019655 Histoplasmosis HSDN C1527344 Dysphonia C1302282 Chromaffin cell neoplasm MalaCards C0034150 Skin purpura C0281479 Primary systemic amyloidosis MalaCards C1549543 Administration method - pain C0008373 Cholesteatoma HSDN C0040822 D tremors C0007787 Transient ischemic attack HSDN C0018772 Deafness C0751666 Canavan disease, infantile OrphaNet|HPO|MalaCards C0020458 Hyperhydrosis C3809007 Cardiofaciocutaneous syndrome 4 MalaCards C0011168 Disorder deglutition C1834569 Jankovic rivera syndrome MalaCards C0751706 Aphasia, progressive nonfluent C0028850 Ocular motility disorders HSDN C3539896 Pelvic pain occurs with urination C0206680 Mesothelioma, cystic HSDN C4084723 Constipation C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) OrphaNet|HPO|MalaCards C4085661 Usual severity nausea C0042830 Perception visual HSDN C4084788 Have dizziness C0035439 Rheumatic heart disease HSDN C0746674 Muscle weakness generalized C1861751 Minicore myopathy, moderate, with hand involvement HPO C0013404 Respiratory difficulty C1266034 Bronchiolo-alveolar carcinoma, non-mucinous UMLS C1000483 Genus anemia C0854176 Malignant hepato-biliary neoplasm MalaCards C0020538 Hbp C2936862 Bardet-biedl syndrome 1 (disorder) MalaCards C4085211 Pain distress question C0001126 Renal tubular acidosis HSDN C1557397 Adverse event associated with pain C0025303 Meningococcal infections HSDN C4084725 Usual severity cough C0024305 Lymphoma, non-hodgkin HSDN C2984058 Have pain C0266015 Congenital digestive system anomalies HSDN C0018772 Deafness C0037926 Compression of spinal cord HSDN C0162298 Stiffness joints C0751202 Cystathionine beta-synthase deficiency disease OrphaNet|HPO C1963086 Confusion adverse event C0019080 Hemorrhage HSDN C4085548 Usual severity dizziness C0013080 Down syndrome HSDN C0030193 Sense of pain C0280367 Adenoid cystic carcinoma of the oral cavity, recurrent UMLS C4084775 Usual severity weight loss C0003850 Arteriosclerosis HSDN C2315100 Pediatric failure to thrive C1859049 Cchs with hirschsprung disease OrphaNet|HPO|MalaCards C0007758 Cerebellar ataxia C0017495 Gerstmann-straussler-scheinker disease MalaCards|UMLS C4084767 Bothered by vomiting C2936913 Porphyria, south african type HPO C4085317 Diarrhea frequency C0025309 Meningoencephalitis HSDN C0015230 Exanthem C0272167 Reticular dysgenesis MalaCards|HPO C0002624 Amnesia retrograde C1290398 Cerebral arterial aneurysm HSDN C0030193 Sense of pain C0553980 Endomyocardial fibrosis HSDN C0016382 Cutaneous vascular engorgement C0263628 Tumoral calcinosis OrphaNet|MalaCards C4084788 Have dizziness C0152054 Therapeutic touch HSDN C4085211 Pain distress question C3245466 Observationvalue - trust HSDN C0034150 Skin purpura C0750426 Wbc elevated HSDN C1557397 Adverse event associated with pain C0242172 Pelvic inflammatory disease HSDN C0034150 Skin purpura C1720922 Respiratory aspiration HSDN C0037316 Not enough sleeping C1956346 Coronary artery disease HSDN C0184567 Pain acute C0031037 Periarthritis HSDN C4042891 Sleep wake disorders C3714509 Nutrition disorders HSDN C0010200 Cough symptom C0349663 Immature malignant teratoma of mediastinum UMLS C0751837 Gait ataxic C1847725 Spinocerebellar ataxia 15 MalaCards|UMLS C0015469 Facial paralysis C0206255 Malaria vaccine HSDN C0600142 Flash hot C0007820 Cerebrovascular disorders HSDN C0011991 Loose stools C1863239 Partial adenosine deaminase deficiency HPO C0278152 Hemifacial spasms C0002940 Aneurysm HSDN C4084766 Vomiting C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO C0003467 Angst C0268632 Homocarnosinosis MalaCards C0557874 Global developmental delay C3502298 Lactic acidosis, fatal infantile MalaCards C4084784 Diarrhea C0043397 Yellow fever, jungle MalaCards C4042891 Sleep wake disorders C0039504 Injuries tendon HSDN C4084775 Usual severity weight loss C0349231 Phobic anxiety disorder HSDN C3665346 Loss sight C0035613 Rift valley fever MalaCards C0022346 Yellow skin C0032763 Post gastrectomy syndrome HSDN C0041105 Jaw spasm C0282606 Myomatous neoplasm HSDN C0149793 Transient monocular blindness C0752235 Lyme neuroborreliosis MalaCards C1384666 Decreased hearing C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0036659 Sensation disorder C0038263 Stereognoses HSDN C0151786 Weakness muscle C0015397 Disorder of eye HSDN C0026838 Spasticity muscle C0520946 Emotional hypersensitivity HSDN C4084766 Vomiting C0268579 Propionic acidemia HPO C4084784 Diarrhea C0042373 Vascular diseases HSDN C0030193 Sense of pain C0040553 Toxocariasis HSDN C0751837 Gait ataxic C0033923 Psychomotor function HSDN C0005745 Blepharoptosis C0206115 Wagr syndrome OrphaNet|HPO C0522224 Palsied C0497552 Congenital neurologic anomalies HSDN C2911647 Weight gain adverse event C0024143 Lupus nephritis HSDN C0026884 Muteness C0006118 Brain neoplasms HSDN C4085210 Usual severity pain C0264134 Hallux limitus HSDN C1963091 Diarrhea adverse event C0086774 Cold hemoglobinuria MalaCards C4084776 Weight loss C0037933 Spinal diseases HSDN C1963184 Nystagmus adverse event C3277723 Joubert syndrome 12 MalaCards C2126231 Light bleeding between periods C0025874 Metrorrhagia UMLS C4084725 Usual severity cough C3161104 Adult plch MalaCards C4084788 Have dizziness C1962976 Ventricular fibrillation adverse event HSDN C2830344 Straining to void C0810038 Genitourinary symptoms and ill-defined conditions UMLS C0424755 Fever symptoms C0152063 Streptobacillus moniliformis infection DiseaseOntology|MalaCards C2024893 Cardiovascular surgery result: fatigue C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0009421 Comatose C0037397 Behavior social HSDN C2242996 Tingling C0549567 Pigmentation disorders HSDN C0221263 Cafe au lait spot C0004135 Ataxia telangiectasia MalaCards|HSDN|HPO C0033377 Caudal displacement C0085261 Proteus syndrome HPO C0151889 Reflexes tendon increased C3539506 Spastic paraplegia 55, autosomal recessive MalaCards C0007758 Cerebellar ataxia C0206663 Neuroectodermal tumor, primitive MalaCards C0021359 Infertility C1847554 Ciliary dyskinesia, primary, 2 (disorder) MalaCards|HPO C0037763 Spasm C0021368 Inflammation HSDN C0020673 Hypothermia (central) (local) C0007453 Cattle disease HSDN C0011991 Loose stools C0025294 Meningococcal meningitis HSDN C0040264 Ear ringing sound C0919267 Ovarian neoplasm HSDN C4084723 Constipation C0030354 Papilloma HSDN C0018681 Headache, cephalalgia C3899671 Childhood cerebellar anaplastic astrocytoma UMLS C0036572 Convulsion C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0012833 Dizzy C0395943 Absence of semicircular canal UMLS C0018681 Headache, cephalalgia C2983719 Nasopharyngeal carcinoma by ajcc v6 stage UMLS C4084802 Usual severity diarrhea C0019829 Hodgkin disease HSDN C2203646 Jaundice C0302280 Adrenogenital syndrome HSDN C1963281 Vomiting adverse event C0305062 Tetanus toxoids HSDN C2024878 Cardiovascular surgery result: dyspnea C0039494 Temporomandibular joint disorders HSDN C0349588 Stature short C0152416 Congenital web of larynx OrphaNet|MalaCards C4084776 Weight loss C0021799 Interprofessional relations HSDN C4084773 Bothered by weight gain C0036349 Paranoid schizophrenia HSDN C0085631 Abnormal excitement C1864112 Huntington disease-like 1 MalaCards|HPO C0043094 Weight gain C0016171 Fistula of intestine, excluding rectum and anus HSDN C2024878 Cardiovascular surgery result: dyspnea C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0038002 Spleen enlargement C0220756 Niemann-pick disease, type c OrphaNet|HPO|MalaCards C4084727 Cough frequency C0022665 Kidney neoplasm HSDN C0013604 Edematous C0016397 Focal infection HSDN C1263846 Attention deficit disorder with hyperactivity C0043379 Xyy karyotype OrphaNet C4084774 Have weight loss C0025205 Melanoma, experimental HSDN C0000737 Abdomen pain C0003873 Rheumatoid arthritis HSDN C1549543 Administration method - pain C0836924 Thrombocytosis HSDN C4042891 Sleep wake disorders C0853697 Neutrophil count decreased HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1297884 Musculo-aponeurotic fibromatosis MalaCards C3463815 Feel fatigue C0010823 Cytomegalovirus infections HSDN C0000737 Abdomen pain C2217039 Stage iiic colon cancer UMLS C4084802 Usual severity diarrhea C0398791 Nijmegen breakage syndrome MalaCards|HPO C0019825 Voice hoarseness C3554605 Mc3dn2 MalaCards C0038002 Spleen enlargement C0087031 Juvenile-onset still disease MalaCards|HPO C0235046 Paresthesia skin C0154725 Oth disorder nervous system UMLS C0019572 Hairiness C0020428 Hyperaldosteronism HSDN C0086565 Liver function abnormal C0268060 Juvenile hemochromatosis OrphaNet|HPO|MalaCards C2203646 Jaundice C0153463 Malig neop oth spec pancreas MalaCards C0036572 Convulsion C0422862 Seizure causing illusions UMLS C0043094 Weight gain C0042487 Venous thrombosis HSDN C0518090 Frequency of pain question C0027720 Nephrosis HSDN C4084725 Usual severity cough C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C0004134 Dyssynergia C3150127 Bardet biedl syndrome 15 HPO C0033774 Skin pruritus C0027663 Neoplasms, multiple primary HSDN C4084724 Usual severity constipation C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0424755 Fever symptoms C0432328 Xeroderma pigmentosum, variant form MalaCards C4085211 Pain distress question C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C2315100 Pediatric failure to thrive C0342783 Deficiency of butyryl-coa dehydrogenase MalaCards|HPO C0460137 Push down or depress C0001206 Acromegaly OrphaNet|HPO|MalaCards C0478144 Other and unspecified speech disturbances C0810273 Other nervous system symptoms and disorders UMLS C0004134 Dyssynergia C1999266 Depression adverse event HSDN C4085211 Pain distress question C0153014 Non-arthropod borne lymphocytic choriomeningitis HSDN C3641756 Have diarrhea C0039231 Tachycardia HSDN C3539022 Pelvic pain decreasing in severity C0243001 Abdominal abscess HSDN C0085610 Bradycardia sinus C1837845 Sick sinus syndrome 1, autosomal recessive MalaCards|HPO C2242996 Tingling C1963138 Hypertension adverse event HSDN C3463815 Feel fatigue C0340629 Aortic aneurysm without mention of rupture nos HSDN C2984058 Have pain C0024919 Behavior, maternal HSDN C0002622 Amnesias C2960129 Vanishing white matter disease MalaCards C0497406 Over weight C0022876 Premature obstetric labor HSDN C0033776 Pregnancy and pruritus C0008370 Cholestasis UMLS C0039070 Collapse fleeting C0006309 Brucellosis HSDN C0018772 Deafness C0010314 Cri-du-chat syndrome MalaCards C0013362 Dysarthrias C1853578 Neuroferritinopathy MalaCards|HPO C1384666 Decreased hearing C0004936 Mental disorders HSDN C0000737 Abdomen pain C2937358 Cerebral hemorrhage HSDN C0020672 Body temperature decreased C0025007 Measles HSDN C3641756 Have diarrhea C1443900 Inhalational botulism OrphaNet|MalaCards C2029884 Hearing loss by exam C0149931 Migraine disorders HSDN C0015672 Decreased energy C0037116 Silicosis HSDN C4084784 Diarrhea C0242634 Diseases primates HSDN C0032914 Toxemia C3463897 Hydatidiform mole, recurrent, 1 MalaCards C2237041 Shox gene with short stature C2720163 Placental steroid sulfatase deficiency MalaCards C0018681 Headache, cephalalgia C0270860 Basilar-type migraine UMLS C0018772 Deafness C0024841 Matrimony, matrimonial HSDN C4084776 Weight loss C0033873 Psychiatry HSDN C0040259 Tinea pedis C0024449 Fungal mycetoma HSDN C1557397 Adverse event associated with pain C1306577 Dies patient HSDN C0007758 Cerebellar ataxia C0001430 Adenoma HSDN C4085211 Pain distress question C0006663 Calcinosis HSDN C3665386 Abnormal vision C0039483 Giant cell arteritis MalaCards|HPO C0042963 Symptoms vomiting C0023470 Myeloid leukemia HSDN C4084784 Diarrhea C0025323 Menorrhagia HSDN C4084774 Have weight loss C0041374 Tumor virus infections HSDN C2029884 Hearing loss by exam C0001973 Alcoholic intoxication, chronic HSDN C4084768 Usual severity vomiting C0000735 Abdominal neoplasms HSDN C1549543 Administration method - pain C0022882 Infection laboratory HSDN C2203646 Jaundice C0854176 Malignant hepato-biliary neoplasm MalaCards C4085661 Usual severity nausea C0036357 Psychology, schizophrenic HSDN C0026821 Cramp C2911643 Encounter due to family history of osteoporosis HSDN C1963091 Diarrhea adverse event C0018051 Gonadal dysgenesis HSDN C0009676 Confusion state C0009375 Colonic neoplasms HSDN C0018775 Hearing loss bilateral C1552527 Clinic / center - developmental disabilities HSDN C1279888 Proteinuria of undiagnosed cause C0010403 Cryoglobulinemia HSDN C0002965 Crescendo angina C0013502 Echinococcosis HSDN C0013390 Cramps menstrual C0438692 Vaginal discharge symptom HSDN C0577564 Mass of lymphoreticular structure C0024248 Cyst lymph UMLS C0003862 Pain joint C0011860 Diabetes mellitus, non-insulin-dependent HSDN C3887873 Hearing loss C0004304 Auditory fatigue HSDN C4085222 Nausea C0080179 Vertebra fracture HSDN C0020538 Hbp C3150733 Long qt syndrome 13 MalaCards|HPO C1961131 Cough adverse event C0036400 Scimitar syndrome HSDN C0700078 Deep tendon reflex decrease C3150413 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 MalaCards C2203646 Jaundice C0497327 Dementia HSDN C4085210 Usual severity pain C0036095 Salivary gland neoplasms HSDN C4084784 Diarrhea C0027092 Myopia HSDN C0518090 Frequency of pain question C0001627 Congenital adrenal hyperplasia HSDN C4084766 Vomiting C0040411 Tongue neoplasms HSDN C0022408 Disorder joint C2749659 Aicardi-goutieres syndrome 5 (disorder) MalaCards C4085210 Usual severity pain C0033348 Language program HSDN C1549543 Administration method - pain C0242659 Female homosexual HSDN C0027498 Nausea vomiting C0043208 Wolman disease OrphaNet|HPO C4084776 Weight loss C0009450 Disease caused by microorganism HSDN C1963087 Constipation adverse event C1956093 Paris-trousseau thrombocytopenia MalaCards C0042963 Symptoms vomiting C1547044 Kind of quantity - smell HSDN C0030552 Paralysis partial C4042784 Feeding and eating disorders HSDN C0034150 Skin purpura C0015423 Eyelid diseases HSDN C0015799 Feminisation C0018054 Gonadal dysgenesis, 46,xy HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0027643 Neoplasm recurrence, local HSDN C0033774 Skin pruritus C0036357 Psychology, schizophrenic HSDN C2984058 Have pain C0013369 Dysentery HSDN C0151889 Reflexes tendon increased C2931006 Congenital disorder of glycosylation type 1l MalaCards C0004604 Pain back C0016057 Fibrosarcoma HSDN C0518090 Frequency of pain question C0007894 Cestode infections HSDN C0013362 Dysarthrias C0796274 Brown-vialetto-van laere syndrome OrphaNet|HPO|MalaCards C0018772 Deafness C0005586 Bipolar disorder HSDN C4084766 Vomiting C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0003550 Broca aphasia C0004303 Auditory disease, central HSDN C0015672 Decreased energy C0034531 Experimental radiation injuries HSDN C1000483 Genus anemia C1832942 Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome (disorder) MalaCards|HPO C4084784 Diarrhea C0015456 Facial dermatoses HSDN C0349489 Fetal hypoxia C0428977 Bradycardia HSDN C4084769 Vomiting frequency C0013182 Drug allergy HSDN C0426579 Anorexia symptom C0043398 Yellow fever, urban MalaCards C2237041 Shox gene with short stature C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C4085211 Pain distress question C0151491 Congenital musculoskeletal anomalies HSDN C0018784 Deafness sensorineural C0021355 Infective otitis externa HSDN C0042025 Urinary incontinence stress C0033575 Prostatic diseases HSDN C4084727 Cough frequency C0039483 Giant cell arteritis MalaCards|HPO C0231528 Muscle pain generalized C2931781 Adenosine monophosphate deaminase deficiency MalaCards C0518090 Frequency of pain question C0001173 Adult pyloric stenosis HSDN C4084766 Vomiting C0004239 Atrial flutter HSDN C2585575 Recurrent abdominal pains C0267868 Recurrent biliary colic UMLS C2919142 Short stature adverse event C0220687 Kbg syndrome MalaCards|HPO C0000737 Abdomen pain C0085681 Hyperphosphatemia (disorder) HSDN C2203646 Jaundice C0008312 Primary biliary cirrhosis OrphaNet|HPO|MalaCards C0022346 Yellow skin C0872996 Q fever vaccine HSDN C0497247 Blood pressure elevation C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C4084725 Usual severity cough C0041315 Tuberculosis, laryngeal HSDN C1557397 Adverse event associated with pain C0015923 Fetal alcohol syndrome HSDN C0018681 Headache, cephalalgia C0026764 Multiple myeloma HSDN C0151908 Dry skin C0917715 Hajdu-cheney syndrome HPO C0000737 Abdomen pain C1332989 Childhood embryonal carcinoma of ovary UMLS C1384666 Decreased hearing C0079744 Diffuse large b-cell lymphoma HSDN C0000737 Abdomen pain C0024198 Lyme disease HSDN C0022660 Acute kidney failure C1956258 Familial thrombotic thrombocytopenic purpura MalaCards C0085636 Light sensitivity C0018609 Hartnup disease OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0338586 Vertebral artery dissection HSDN C4085210 Usual severity pain C0024138 Lupus erythematosus, discoid HSDN C0557874 Global developmental delay C1860157 Elejalde disease MalaCards C0007758 Cerebellar ataxia C4015261 Polyendocrine-polyneuropathy syndrome MalaCards C0027796 Neuralgias C0019080 Hemorrhage HSDN C0413252 Hypothermia due to exposure C0008073 Developmental disabilities HSDN C0023885 Liver abscess C0030360 Papillon-lefevre disease MalaCards|HPO C0015402 Hemorrhage eye C0020452 Hyperemia HSDN C4018871 Abnormality of the respiratory system C1704375 Hypophosphatemic rickets MalaCards|HPO C1962972 Proteinuria adverse event C0005659 Bite sting HSDN C0018681 Headache, cephalalgia C0035258 Restless legs syndrome HSDN C0497406 Over weight C0023434 Chronic lymphocytic leukemia HSDN C0242936 Center pain C0079772 T-cell lymphoma HSDN C0004604 Pain back C0030297 Pancreatic neoplasm MalaCards|HSDN C3539892 Pelvic pain in front C0042373 Vascular diseases HSDN C0151786 Weakness muscle C0342784 Pearson's marrow-pancreas syndrome HPO C3815497 Cough C0027429 Nasal obstruction present finding HSDN C2024893 Cardiovascular surgery result: fatigue C0555202 Malignant lymphoma - lymphocytic, intermediate differentiation OrphaNet|HPO|MalaCards C2984058 Have pain C1412084 Abcd1 gene HSDN C0013604 Edematous C1415369 Gulop gene HSDN C0018784 Deafness sensorineural C0035439 Rheumatic heart disease HSDN C3463815 Feel fatigue C1837218 Cleft palate, isolated HSDN C2024878 Cardiovascular surgery result: dyspnea C0021368 Inflammation HSDN C1549543 Administration method - pain C0003827 Art therapies HSDN C0022346 Yellow skin C1335255 Pretext stage 1 hepatoblastoma UMLS C0015468 Face pain C0031090 Periodontal diseases HSDN C1963086 Confusion adverse event C0041321 Tuberculosis, miliary HSDN C4018871 Abnormality of the respiratory system C0456487 Peutz jeghers polyp MalaCards C0034151 Hyperglobulinemic purpura C0002726 Amyloidosis HSDN C0030193 Sense of pain C0019187 Hepatitis, alcoholic HSDN C0232462 Appetite decrease C1411077 Ragpicker's disease MalaCards C0587246 Extremity weakness C1850386 Giant axonal neuropathy 1 MalaCards C0151889 Reflexes tendon increased C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards C0728710 Pupil constriction observed C0042826 Field visual HSDN C0042571 Vertigo subjective C0014038 Encephalitis HSDN C0035229 Respiratory function impaired C1868678 Thanatophoric dysplasia, type i (disorder) OrphaNet|HPO|MalaCards C0020505 Excessive eating C0018799 Heart diseases HSDN C0557874 Global developmental delay C0206663 Neuroectodermal tumor, primitive MalaCards C0233514 Behavior abnormal C0017083 Gangliosidoses MalaCards C0013132 Drooling C0038325 Stevens-johnson syndrome OrphaNet|HPO C0520909 Ponv C0019080 Hemorrhage HSDN C0010520 Skin cyanosis C0001430 Adenoma HSDN C4085317 Diarrhea frequency C0020507 Hyperplasia HSDN C0020538 Hbp C2931468 Cystic hamartomata of lung and kidney OrphaNet|MalaCards C4084769 Vomiting frequency C0152998 Acute nonparalytic poliomyelitis, poliovirus, unspecified type DiseaseOntology|MalaCards C3665492 Pigmentations C0859920 Hair follicle neoplasm MalaCards C0034124 Pupillary disorder C2984299 Asthma pathway HSDN C2203646 Jaundice C0233629 Thinking and speaking disturbances HSDN C1549543 Administration method - pain C0019021 Hemoglobin c disease HSDN C4084769 Vomiting frequency C0267830 Pyogenic liver abscess HSDN C0085602 Polydypsia C1253937 Pericardial effusion HSDN C0233794 Memory impaired C0027145 Myxedema MalaCards C1963065 Apnea adverse event C0038160 Staphylococcal infections HSDN C4084784 Diarrhea C0037198 Sinus thrombosis, intracranial HSDN C0009421 Comatose C0007772 Intracranial arteriovenous malformation HSDN C4085210 Usual severity pain C0002992 Angiomatosis HSDN C3274924 Have been coughing C0600467 Neurogenic inflammation HSDN C0034933 Abnormal reflexes C3887662 Intraspinal neoplasm HSDN C4084774 Have weight loss C0151467 Addisonian crisis OrphaNet|MalaCards C1549543 Administration method - pain C0019087 Hemorrhagic disorders HSDN C0037316 Not enough sleeping C0025284 Meningeal neoplasms HSDN C0003862 Pain joint C0025303 Meningococcal infections HSDN C0454644 Delayed language development C3553582 Seckel syndrome 6 MalaCards C0231712 Gait waddling C3809049 Spinal muscular atrophy, lower extremity-predominant, 2, autosomal dominant UMLS C4085549 Dizziness C0035439 Rheumatic heart disease HSDN C0003862 Pain joint C0162526 Aids-related opportunistic infections HSDN C1963093 Dizziness adverse event C0997768 Glaucoma HSDN C0349588 Stature short C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0031046 Pericarditis HSDN C0085602 Polydypsia C0036341 Schizophrenia HSDN C1384666 Decreased hearing C3554163 Deafness, autosomal recessive 18b MalaCards C0917816 Deficiency mental C2931850 Aase smith syndrome 2 MalaCards|HPO C0030193 Sense of pain C0280402 Laryngeal verrucous carcinoma, recurrent UMLS C0002962 Angina C0022373 Disease, jejunal HSDN C0424755 Fever symptoms C0032797 Postpartum hemorrhage HSDN C0002962 Angina C0018099 Gout HSDN C4084774 Have weight loss C0020564 Hypertrophy HSDN C3541349 Syncope C0042029 Urinary tract infection HSDN C3539893 Pelvic pain occurs with intercourse C0003873 Rheumatoid arthritis HSDN C0018681 Headache, cephalalgia C0276119 Q-fever pneumonia MalaCards C0036572 Convulsion C0004610 Bacteremia HSDN C0018784 Deafness sensorineural C0027666 Neoplasms, radiation-induced HSDN C0013404 Respiratory difficulty C0206732 Epithelioid hemangioendothelioma HSDN C0234146 Absent reflex C1858280 Charcot-marie-tooth neuropathy, type 4b2, with early-onset glaucoma HPO C0241137 Skin pallor C0032249 Plummer vinson syndrome OrphaNet|HSDN|MalaCards C0151740 Intracranial hypertension C0023092 Lassa fever MalaCards C0008031 Pain chest C1970472 Pulmonary alveolar proteinosis, acquired MalaCards|UMLS C1549543 Administration method - pain C0000786 Spontaneous abortion HSDN C4084769 Vomiting frequency C0024919 Behavior, maternal HSDN C1961131 Cough adverse event C1963067 Atrial fibrillation adverse event HSDN C0020455 Hypergammaglobulinemia C0039446 Telangiectasis HSDN C0401020 Intra-abdominal collection C0586377 Peritonitis post-procedural intra-abdominal sepsis UMLS C0004604 Pain back C1548777 Specimen reject reason - hemolysis HSDN C3641756 Have diarrhea C1443901 Intestinal botulism OrphaNet|MalaCards C2315100 Pediatric failure to thrive C0015625 Fanconi anemia HSDN C1963237 Insomnia adverse event C0751362 Narcolepsy-cataplexy syndrome MalaCards C0015672 Decreased energy C0007873 Uterine cervical neoplasm HSDN C0232493 Epigastric pain C0268039 Ketoacidosis alcoholic UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003486 Aortic aneurysm HSDN C0008031 Pain chest C0585274 Periodic syndrome OrphaNet|HPO C0024031 Back pain lower back C3163620 Hypotension adverse event HSDN C0751837 Gait ataxic C0032453 Polychondritis, relapsing HSDN C2911645 Weight loss adverse event C0036992 Short bowel syndrome HSDN C4084725 Usual severity cough C1535917 Nipah virus infection MalaCards C0270948 Neurogenic muscular atrophy C1861753 Multiminicore disease, moderate, with hand involvement HPO C0018772 Deafness C0950123 Inborn genetic disease HSDN C0002624 Amnesia retrograde C0556346 Binge drinking HSDN C0024031 Back pain lower back C0007682 Cns disorder HSDN C0026826 High muscle tone C0205710 Alpers syndrome (disorder) MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C1963234 Serum sickness adverse event HSDN C0241137 Skin pallor C0393706 Early infantile epileptic encephalopathy with suppression bursts MalaCards C1959630 Eye pain adverse event C0524801 Retinal neoplasms HSDN C1963170 Hypothermia adverse event C0040053 Thrombosis HSDN C4084802 Usual severity diarrhea C0042133 Uterine fibroids HSDN C2911645 Weight loss adverse event C0032584 Polyps HSDN C4020887 Photodysphoria C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0027497 Queasy C3150933 Hyperaldosteronism, familial, type iii MalaCards C1963137 Hydrocephalus adverse event C4015558 Temple syndrome MalaCards C0009398 Color vision defects C0012746 Dissociative disorder HSDN C0015672 Decreased energy C1290398 Cerebral arterial aneurysm HSDN C1145670 Failure respiratory C0221056 Adult type dermatomyositis OrphaNet|MalaCards C0015672 Decreased energy C0302148 Blood clot HSDN C1963065 Apnea adverse event C0085417 Epilepsy, complex partial HSDN C4085222 Nausea C0009374 Colonic disease, functional HSDN C0018991 Paralysis one side of body C0028242 Nocardia infections HSDN C4084773 Bothered by weight gain C0020545 Hypertension, renovascular HSDN C2984058 Have pain C0034362 Q fever HSDN C0086439 Activity decreased C0393571 Multiple system atrophy HSDN C0426579 Anorexia symptom C0043121 Wernicke encephalopathy HSDN C0015469 Facial paralysis C0153017 Encephalitis varicella HSDN C3539892 Pelvic pain in front C0041960 Ureterocele HSDN C0857305 Thrombocytopenia purpura C1636667 Disorder characterized by eosinophilia HSDN C4085642 Level of joint stiffness C0265210 Weaver syndrome OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0031212 Personality disorders HSDN C0042798 Vision dim C0010038 Corneal opacity HSDN C0003079 Pupillary inequality C0349606 Central nervous system cysts HSDN C0016204 Fart C0020538 Hypertensive disease HSDN C0020903 Illusion C0011581 Depressive disorder HSDN C4084768 Usual severity vomiting C1306759 Eosinophilic disorder HSDN C0042963 Symptoms vomiting C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C0151786 Weakness muscle C0085315 Toxoplasmosis, cerebral HSDN C1971624 Appetite absent C0302362 Brucella melitensis infection MalaCards C4084802 Usual severity diarrhea C0009442 Common bile duct neoplasms HSDN C1549543 Administration method - pain C0085073 Prosthesis-related infection HSDN C1856661 Cornea cloudy C2673375 Mucolipidosis iii alpha beta, atypical HPO C1963071 Back pain adverse event C0027686 Pathologic neovascularization HSDN C0030486 Extremity paralysis, lower C0026848 Myopathy HSDN C1000483 Genus anemia C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C4084802 Usual severity diarrhea C0001721 Emotional affect HSDN C0008031 Pain chest C0231644 Chest pain xiphodynia UMLS C2024893 Cardiovascular surgery result: fatigue C0011848 Diabetes insipidus HSDN C4085317 Diarrhea frequency C1270972 Mild cognitive disorder HSDN C0000727 Abdomen acute C0040034 Thrombocytopenia HSDN C0231218 Malaise generalized C0861854 Adenosquamous bile duct carcinoma UMLS C4085211 Pain distress question C0029295 Oropharyngeal neoplasms HSDN C0036572 Convulsion C0024205 Lymphadenitis HSDN C3665492 Pigmentations C3661523 Congenital intestinal aganglionosis MalaCards C0034155 Thrombotic thrombocytopenic purpura C0161410 Accessory nerve injuries HSDN C0034933 Abnormal reflexes C0030472 Paraneoplastic syndromes HSDN C0026205 Pupillary constriction C0026205 Miosis disorder MalaCards C0038002 Spleen enlargement C0002895 Anemia, sickle cell MalaCards|HPO C0026821 Cramp C0700095 Central neuroblastoma HSDN C0030193 Sense of pain C0022667 Papillary necrosis HSDN C3539022 Pelvic pain decreasing in severity C0751792 Trauma, nervous system HSDN C3665492 Pigmentations C0153633 Malignant neoplasm of brain MalaCards C0016204 Fart C1881674 Medical device emits smoke HSDN C0003862 Pain joint C0023890 Liver cirrhosis HSDN C3146279 Coma C0042345 Varicosity HSDN C4084766 Vomiting C0016053 Fibromyalgia HSDN C0036659 Sensation disorder C0039319 Tarsal tunnel syndrome HSDN C0424755 Fever symptoms C0036830 Serum sickness HSDN C0020672 Body temperature decreased C0021051 Immunologic deficiency syndromes HSDN C0518090 Frequency of pain question C0560651 Spinal cord syndrome central HSDN C1963281 Vomiting adverse event C0007766 Intracranial aneurysm HSDN C0557874 Global developmental delay C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C0349489 Fetal hypoxia C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0013604 Edematous C0042065 Genitourinary neoplasms HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0013481 Ebstein anomaly OrphaNet|HPO|MalaCards C1963077 Bone pain adverse event C1838657 Vitamin d hydroxylation-deficient rickets, type 1b HPO C1549543 Administration method - pain C0877149 Pain patellofemoral syndrome HSDN C0016204 Fart C0012979 Canine disease HSDN C0241210 Speaking delay C1850985 Fragile site 16p12 HPO C4085317 Diarrhea frequency C0948089 Acute coronary syndrome HSDN C0221166 Paraparesis C1963274 Vasculitis adverse event HSDN C0581358 Gastric spasm C0156084 Gastric dysfunction UMLS C1963167 Memory impairment adverse event C1843014 Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques HPO C2984058 Have pain C0151814 Coronary occlusion HSDN C1963064 Anxiety adverse event C0175702 Williams syndrome OrphaNet|HPO|MalaCards C3665492 Pigmentations C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C2984058 Have pain C0221269 Pseudolymphoma HSDN C1963063 Anorexia adverse event C0011853 Diabetes mellitus, experimental HSDN C3815497 Cough C0948089 Acute coronary syndrome HSDN C4084775 Usual severity weight loss C0011875 Diabetic angiopathies HSDN C0018777 Deafness, conductive C0393484 Rasmussen syndrome MalaCards C0036572 Convulsion C2936741 Syndrome xxyy MalaCards C4084776 Weight loss C0027814 Neuritis, autoimmune, experimental HSDN C0271215 Blindness legal C2880931 Proliferative vitreo-retinopathy MalaCards C0151686 Growth retardation C0432267 Tricho thiodystrophy disorder MalaCards C0030193 Sense of pain C0033680 Protein-losing enteropathies HSDN C4084774 Have weight loss C1335686 Neuroendocrine neoplasm of rectum MalaCards C4084776 Weight loss C1175175 Severe acute respiratory syndrome HSDN C0018784 Deafness sensorineural C2937358 Cerebral hemorrhage HSDN C0013404 Respiratory difficulty C0274435 Transfusion reaction HSDN C0014724 Burping C0034929 Reflex HSDN C0009421 Comatose C0022650 Kidney calculi HSDN C1384666 Decreased hearing C0020433 Hyperbilirubinemia HSDN C2700617 Irritation - emotion C0342646 Vitamin d-dependent rickets, type 2a HPO C4050613 Anxiety C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0454644 Delayed language development C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C4084766 Vomiting C0273058 Traumatic intracranial hemorrhage HSDN C0002622 Amnesias C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0035232 Diaphragmatic paralysis C1266101 Thymic epithelial tumor OrphaNet C4084724 Usual severity constipation C0038661 Suicide HSDN C4084723 Constipation C0034063 Pulmonary edema HSDN C2315100 Pediatric failure to thrive C0342765 D-glyceric aciduria HPO C0023380 Lethargy C3554067 Combined oxidative phosphorylation deficiency 11 MalaCards|UMLS C0234373 Fine tremor C1970840 Leukoencephalopathy with metaphyseal chondrodysplasia MalaCards|UMLS C3539896 Pelvic pain occurs with urination C0003873 Rheumatoid arthritis HSDN C2984058 Have pain C0085423 Gram-negative bacterial infections HSDN C2911647 Weight gain adverse event C0024117 Chronic obstructive airway disease HSDN C1557397 Adverse event associated with pain C0027626 Neoplasm invasiveness HSDN C2984057 Have nausea C0002736 Amyotrophic lateral sclerosis HSDN C1971624 Appetite absent C0005426 Biliary tract neoplasm HSDN C4085661 Usual severity nausea C0033817 Pseudomonas infections HSDN C0004134 Dyssynergia C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|UMLS|HPO|MalaCards C0027769 Tension nervous C0004044 Asphyxia UMLS C0037763 Spasm C1548578 Location characteristic id - smoking HSDN C0030193 Sense of pain C1254288 Anthrax HSDN C0242936 Center pain C0003857 Congenital arteriovenous malformation HSDN C0557874 Global developmental delay C1846059 Roifman syndrome MalaCards C0030193 Sense of pain C0041328 Renal tuberculosis HSDN C0242936 Center pain C0221391 Melanosis coli HSDN C0030193 Sense of pain C4047672 Meralgia paresthetica of left leg UMLS C0020580 Decreased sensation C3714535 Malocclusion, angle class ii HSDN C4084802 Usual severity diarrhea C1855869 Autoimmune polyendocrinopathy syndrome, type i, autosomal dominant HPO C0234523 Apraxia, classic C0035053 Spontaneous remission HSDN C0413252 Hypothermia due to exposure C0011854 Diabetes mellitus, insulin-dependent HSDN C4084724 Usual severity constipation C0040034 Thrombocytopenia HSDN C0002965 Crescendo angina C0019348 Herpes simplex infections HSDN C0518090 Frequency of pain question C0027809 Neurilemmoma MalaCards C0476273 Distress respiratory C0020192 Hyaline membrane disease MalaCards C0003862 Pain joint C0342907 Sitosterolemia MalaCards|HPO C3665346 Loss sight C1970848 Phosphoglycerate kinase 1 deficiency MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0030521 Parathyroid neoplasms HSDN C0020305 Fetal edema C2936421 Sex chromosome disorders of sex development HSDN C4085210 Usual severity pain C0025309 Meningoencephalitis HSDN C0007758 Cerebellar ataxia C0007795 Diffuse cerebral sclerosis of schilder MalaCards|HSDN C0085631 Abnormal excitement C0024121 Lung neoplasms HSDN C0018772 Deafness C1844853 Brachytelephalangic chondrodysplasia punctata HPO C0042963 Symptoms vomiting C0019069 Hemophilia a HSDN C0522224 Palsied C0038436 Post-traumatic stress disorder HSDN C0700078 Deep tendon reflex decrease C0013264 Muscular dystrophy, duchenne HPO C0242936 Center pain C2963140 Arteriovenous fistula in use with two needles HSDN C2936821 Spinal cerebrospinal fluid leak C0001080 Achondroplasia HSDN C0011991 Loose stools C0003496 Aortic rupture HSDN C0027498 Nausea vomiting C3887678 Cpnet MalaCards C1963087 Constipation adverse event C0018801 Heart failure HSDN C0271215 Blindness legal C0025286 Meningioma MalaCards C0037763 Spasm C0036202 Sarcoidosis HSDN C4085222 Nausea C0085096 Peripheral vascular diseases HSDN C3641755 Have constipation C0041948 Uremia HSDN C0085642 Asphyxia reticularis C3814530 Skin vesicle HSDN C0577567 Mass of urogenital structure C0009663 Condylomata acuminata UMLS C0151827 Pain eye C0015467 Neuralgia facial HSDN C0398650 Idiopathic thrombocytopenia purpura C0030567 Parkinson disease HSDN C1963184 Nystagmus adverse event C0221061 Behr syndrome OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0162666 Mitochondrial encephalomyopathies HSDN C0424755 Fever symptoms C0020981 Angioimmunoblastic lymphadenopathy HSDN C0013404 Respiratory difficulty C0150011 Inadequate or impaired airway clearance UMLS C0018520 Breath odor C0030372 Fever, pappataci HSDN C0035232 Diaphragmatic paralysis C0001418 Adenocarcinoma HSDN C3815497 Cough C0001584 Adolescent psychology HSDN C4084776 Weight loss C0003467 Anxiety HSDN C0005779 Clotting C0268307 Conjugated hyperbilirubinemia MalaCards C0032227 Effusion pleural C0566602 Primary sclerosing cholangitis MalaCards|HPO C0018784 Deafness sensorineural C0162429 Malnutrition HSDN C4085210 Usual severity pain C0024228 Lymphatic diseases HSDN C4084766 Vomiting C0032269 Pneumococcal infections HSDN C0241137 Skin pallor C0272051 Xerocytosis HPO C0518090 Frequency of pain question C0152025 Polyneuropathy HSDN C4085661 Usual severity nausea C0305062 Tetanus toxoids HSDN C0013395 Indigestion C0033975 Psychotic disorders HSDN C0036572 Convulsion C3494991 Dravet syndrome, non-intractable UMLS C0026838 Spasticity muscle C0008925 Cleft palate HSDN C4050613 Anxiety C1527168 Bonnevie-ullrich syndrome MalaCards C0020505 Excessive eating C0028765 Behavior obsessive HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0340629 Aortic aneurysm without mention of rupture nos HSDN C2237041 Shox gene with short stature C2713447 Hyperpotassemia and hypertension, familial MalaCards C0026826 High muscle tone C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0085293 Hepatitis e HSDN C0038868 Supranuclear palsy progressive C0270952 Muscular dystrophy, oculopharyngeal HSDN C0349588 Stature short C1853566 Genitopatellar syndrome MalaCards|HPO C0277959 Hair coarseness C3150736 Congenital disorder of glycosylation, type iij MalaCards|HPO C0039070 Collapse fleeting C0018802 Congestive heart failure UMLS C0917816 Deficiency mental C1848439 Mental retardation wolff type MalaCards C1549543 Administration method - pain C0015806 Femur neck fracture HSDN C0040264 Ear ringing sound C0012691 Dislocations HSDN C4084725 Usual severity cough C0264423 Asthma, occupational HSDN C2911645 Weight loss adverse event C0018099 Gout HSDN C0030486 Extremity paralysis, lower C0008073 Developmental disabilities HSDN C1963170 Hypothermia adverse event C0009404 Colorectal neoplasms HSDN C0022346 Yellow skin C3150672 Arthrogryposis, renal dysfunction, and cholestasis 2 MalaCards|HPO|UMLS C0349588 Stature short C1842465 Lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones OrphaNet|MalaCards C0027497 Queasy C0022336 Creutzfeldt-jakob disease HSDN C0233794 Memory impaired C1762616 Meningioma, benign, no icd-o subtype MalaCards C0036572 Convulsion C0155338 Total ophthalmoplegia MalaCards C0277959 Hair coarseness C0877024 Schimke immunoosseous dysplasia MalaCards|HPO C4085661 Usual severity nausea C0002986 Fabry disease MalaCards|HPO C1961131 Cough adverse event C0206703 Carcinoma, giant cell HSDN C0011991 Loose stools C0037397 Behavior social HSDN C2984057 Have nausea C0002991 Cutaneous fibrous histiocytoma HSDN C4084725 Usual severity cough C0019348 Herpes simplex infections HSDN C0413252 Hypothermia due to exposure C1090821 Sepsis (invertebrate) HSDN C0037315 Breathing disorder during sleeping C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C4084767 Bothered by vomiting C0037274 Dermatologic disorders HSDN C0023015 Language handicap C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards C0026821 Cramp C0004352 Autistic disorder HSDN C4085548 Usual severity dizziness C0033968 Psychotherapeutic technique HSDN C0043144 Wheeze C0264413 Late onset asthma UMLS C0000727 Abdomen acute C1956346 Coronary artery disease HSDN C0030794 Pelvis pain C0022661 Kidney failure, chronic HSDN C0234428 Consciousness disturbance C0751667 Canavan disease, juvenile MalaCards C0026838 Spasticity muscle C3495422 Finding relating to sexuality and sexual activity HSDN C0018524 Hallucinate C0517555 Venous thrombosis after immobility HSDN C4084776 Weight loss C0393576 Chorea acanthocytosis syndrome MalaCards|HPO C0041657 Consciousness loss C0037313 Sleep HSDN C4084766 Vomiting C0007099 Carcinoma in situ HSDN C1963091 Diarrhea adverse event C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0042963 Symptoms vomiting C0040034 Thrombocytopenia UMLS C0476273 Distress respiratory C1334666 Mediastinal malignant non-seminomatous germ cell neoplasm UMLS C1069915 Vertigo C0086957 Naffziger syndrome HSDN C0426579 Anorexia symptom C1999266 Depression adverse event HSDN C4084769 Vomiting frequency C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C2984058 Have pain C0023051 Laryngeal diseases HSDN C4084788 Have dizziness C0751815 Carotid artery, internal, dissection HSDN C3541349 Syncope C1706377 Memory device component HSDN C0015672 Decreased energy C0038220 Status epilepticus HSDN C0002962 Angina C0017416 Genital neoplasms, female HSDN C3665492 Pigmentations C0334443 Epithelioid cell melanoma MalaCards C0020578 Hyperventilate C0520676 Premenstrual dysphoric disorder HSDN C4084897 Sleep disturbance subordinate domain C2678194 Mental retardation, x-linked, syndromic, christianson type HPO C0333648 Abiotrophy C0011164 Abnormal degeneration UMLS C0018784 Deafness sensorineural C1855310 Megaepiphyseal dwarfism MalaCards C0000737 Abdomen pain C0206767 Neoplasms, cystic, mucinous, and serous HSDN C0812426 Kidney problem C0748277 Renal cell carcinoma metastatic stage stageval UMLS C0231218 Malaise generalized C0302363 Bang disease MalaCards C0013604 Edematous C0037315 Sleep apnea syndromes HSDN C1999266 Depression adverse event C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards|HPO C4084766 Vomiting C0517555 Venous thrombosis after immobility HSDN C3829611 Nausea frequency C0039971 Thirst HSDN C1963063 Anorexia adverse event C0346407 Pancreatic polypeptide-oma MalaCards C0030552 Paralysis partial C0005695 Bladder neoplasm HSDN C3463815 Feel fatigue C0038454 Cerebrovascular accident HSDN C2911645 Weight loss adverse event C1306577 Dies patient HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C2096293 Ent surgical result ear vertigo C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C1963091 Diarrhea adverse event C0268384 Familial amyloid neuropathy, portuguese type MalaCards C4084766 Vomiting C0018799 Heart diseases HSDN C0033774 Skin pruritus C0861859 Bile duct signet ring cell carcinoma UMLS C0013421 Dystonia C1419767 Rss gene HSDN C0039070 Collapse fleeting C4085311 Depression - recess HSDN C3887638 Failure to thrive in infant C0432269 Lenz majewski hyperostotic dwarfism MalaCards|HPO C2984057 Have nausea C1881674 Medical device emits smoke HSDN C0151908 Dry skin C0343057 Keratosis pilaris decalvans HPO C0085593 Chill C0035592 Infection, rickettsiaceae MalaCards C0010520 Skin cyanosis C0037929 Spinal cord injuries HSDN C0027497 Queasy C0008073 Developmental disabilities HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0151740 Intracranial hypertension HSDN C1963086 Confusion adverse event C0036357 Psychology, schizophrenic HSDN C0344428 Ventricular tachycardia by ecg finding C0340485 Familial ventricular tachycardia MalaCards C0040822 D tremors C0036974 Shock HSDN C0001825 Agraphia C0702221 Tactual discrimination HSDN C0030552 Paralysis partial C0238358 Hypokalemic periodic paralysis HSDN C0000737 Abdomen pain C2945560 Hemolytic HSDN C0038868 Supranuclear palsy progressive C0013363 Dysautonomia HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0007137 Squamous cell carcinoma HSDN C0020578 Hyperventilate C0010709 Cyst HSDN C0007758 Cerebellar ataxia C0010267 Cranial nerve neoplasms HSDN C0036572 Convulsion C0341957 Eclampsia; during labor UMLS C3463815 Feel fatigue C0039980 Chest injury HSDN C4085211 Pain distress question C0206698 Cholangiocarcinoma HSDN C0016204 Fart C0034885 Rectal neoplasms HSDN C2203646 Jaundice C2981150 Uranostaphyloschisis HSDN C0424755 Fever symptoms C0993582 Arthritis, experimental HSDN C4084768 Usual severity vomiting C0001314 Acute disease HSDN C0033774 Skin pruritus C0079474 Hallopeau-siemens disease MalaCards C1963180 Neck pain adverse event C0041327 Tuberculosis, pulmonary HSDN C0020578 Hyperventilate C1956346 Coronary artery disease HSDN C0030552 Paralysis partial C0003811 Cardiac arrhythmia HSDN C4084776 Weight loss C0032914 Pre-eclampsia HSDN C0030200 Intractable pain C0036202 Sarcoidosis HSDN C0150055 Pain chronic C0036690 Septicemia HSDN C4084769 Vomiting frequency C1963274 Vasculitis adverse event HSDN C4085317 Diarrhea frequency C0040425 Tonsillitis HSDN C1963091 Diarrhea adverse event C0018794 Heart block HSDN C0018681 Headache, cephalalgia C3697162 Chronic post-concussion headache UMLS C0018991 Paralysis one side of body C1547940 Specimen source codes - ulcer HSDN C4084768 Usual severity vomiting C0003864 Arthritis HSDN C4084775 Usual severity weight loss C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0522224 Palsied C0020120 Engineering humans HSDN C0015469 Facial paralysis C0273485 Cranial nerve ix injury HSDN C0023380 Lethargy C0016724 Froehlich's syndrome HSDN C0042963 Symptoms vomiting C0405076 Other preg.vomiting-not deliv. UMLS C0600142 Flash hot C0042138 Uterine neoplasms HSDN C0151825 Ostalgia C0265253 Stickler syndrome (disorder) OrphaNet|MalaCards C0018784 Deafness sensorineural C0042018 Urinary calculi HSDN C0027796 Neuralgias C0003615 Appendicitis HSDN C0026838 Spasticity muscle C0035243 Respiratory tract infections HSDN C0009806 Constipate C0036357 Psychology, schizophrenic HSDN C4084784 Diarrhea C0016952 Galactosemias MalaCards C0011175 Deficient fluid volume C0342869 Deficiency of acetyl-coa acyltransferase (disorder) MalaCards C0036572 Convulsion C2678046 Mental retardation, x-linked, syndromic, turner type HPO C0035078 Failure kidney C2720163 Placental steroid sulfatase deficiency MalaCards C3641756 Have diarrhea C0020192 Hyaline membrane disease HSDN C0476273 Distress respiratory C0035410 Rhabdomyolysis UMLS C0042024 Urine incontinence C0007820 Cerebrovascular disorders HSDN C0035078 Failure kidney C1852456 Cryoglobulinemia, familial mixed OrphaNet|MalaCards C3898969 Have been vomiting C0003615 Appendicitis DiseaseOntology|HSDN|MalaCards C0009792 Consciousness disorder C0023418 Leukemia HSDN C4084774 Have weight loss C0026552 Morphine dependence HSDN C4084724 Usual severity constipation C0268412 Infantile hypophosphatasia MalaCards|HPO C0010520 Skin cyanosis C0010068 Coronary heart disease HSDN C0023380 Lethargy C0023067 Laryngitis HSDN C0747556 Pharyngitis recurrent C1956391 Temporal arteritis MalaCards|HPO C0032285 Pneum C0271576 Immunoglobulinemia with isolated somatotropin deficiency HPO C2024878 Cardiovascular surgery result: dyspnea C1704272 Benign prostatic hyperplasia HSDN C0042571 Vertigo subjective C0027051 Myocardial infarction HSDN C0042571 Vertigo subjective C0013502 Echinococcosis HSDN C0008031 Pain chest C0023473 Myeloid leukemia, chronic HSDN C0032617 High urine output C0010276 Craniopharyngioma HSDN C4084723 Constipation C0018939 Hematological disease HSDN C0010520 Skin cyanosis C0010074 Coronary vessel anomalies HSDN C3898969 Have been vomiting C0233629 Thinking and speaking disturbances HSDN C0020538 Hbp C1855607 Keutel syndrome MalaCards C0043094 Weight gain C0040427 Tooth abnormalities HSDN C0020672 Body temperature decreased C0034531 Experimental radiation injuries HSDN C0013604 Edematous C0041582 Ulcer HSDN C0026821 Cramp C0023343 Leprosy HSDN C0042798 Vision dim C0267372 Intestinal lymphatic obstruction MalaCards C0033774 Skin pruritus C0013080 Down syndrome HSDN C0013604 Edematous C0018767 Auditory sense HSDN C0518090 Frequency of pain question C1852551 Epithelial recurrent erosion dystrophy MalaCards|HPO C0026858 Musculoskeletal pain C3541994 Drug hypersensitivity syndrome HSDN C0241210 Speaking delay C3495554 Homocarnosinase deficiency MalaCards C3463815 Feel fatigue C0041316 Lymph node tuberculosis DiseaseOntology|MalaCards C1963249 Tinnitus adverse event C0013990 Pathological accumulation of air in tissues HSDN C0015469 Facial paralysis C1550672 Specimen type - ulcer HSDN C0017181 Gastrointestinal bleed C0022739 Klippel-trenaunay-weber syndrome OrphaNet|MalaCards C0003962 Ascites C0028064 Niemann-pick diseases MalaCards C4084776 Weight loss C0036118 Salmonella infections, animal HSDN C1963071 Back pain adverse event C0012979 Canine disease HSDN C0413252 Hypothermia due to exposure C0009319 Colitis HSDN C0030193 Sense of pain C0007117 Basal cell carcinoma HSDN C4085548 Usual severity dizziness C0029132 Disorder of the optic nerve HSDN C2237041 Shox gene with short stature C0265303 Acrocephalopolysyndactyly type iv MalaCards C1963170 Hypothermia adverse event C0031154 Peritonitis HSDN C0522224 Palsied C0025500 Mesothelioma HSDN C0026825 Flaccidity muscle C1855663 Kaufman oculocerebrofacial syndrome MalaCards C0424755 Fever symptoms C0039614 Tetanus HSDN C0015672 Decreased energy C1963134 Hemorrhoids adverse event HSDN C0042024 Urine incontinence C1706192 Sulfatidosis MalaCards C0027498 Nausea vomiting C0034494 Rabies (disorder) OrphaNet|MalaCards C0004604 Pain back C0158683 Polycystic liver disease MalaCards|HPO C2984058 Have pain C1963107 Euphoria adverse event HSDN C0005745 Blepharoptosis C0796081 Growth mental deficiency syndrome of myhre MalaCards C0011168 Disorder deglutition C0406557 Poikiloderma of kindler OrphaNet|HPO|MalaCards C0018991 Paralysis one side of body C0018671 Head and neck neoplasms HSDN C2024893 Cardiovascular surgery result: fatigue C1704272 Benign prostatic hyperplasia HSDN C0024031 Back pain lower back C0038354 Stomach diseases HSDN C0027497 Queasy C0009319 Colitis HSDN C0006370 Bulimia C0014859 Esophageal neoplasms HSDN C0019521 Hiccoughs C0042338 Herpesvirus 3, human HSDN C0030554 Abnormal sensation C0037369 Smoking HSDN C0035078 Failure kidney C0936273 Familial amyloid polyneuropathy, type iv MalaCards C0018681 Headache, cephalalgia C1336348 Stage iva carcinoma of nasopharynx UMLS C4084724 Usual severity constipation C1999266 Depression adverse event HSDN C0030193 Sense of pain C0016085 Filariasis HSDN C2984058 Have pain C0040583 Tracheal stenosis HSDN C0004093 Asthenia C0025345 Menstruation disturbances HSDN C1963281 Vomiting adverse event C0029134 Optic neuritis HSDN C0011991 Loose stools C0334489 Pancreatoblastoma OrphaNet|MalaCards C0000737 Abdomen pain C0011875 Diabetic angiopathies HSDN C0086437 Joint hypermobility C3810012 Rienhoff syndrome MalaCards C0018681 Headache, cephalalgia C0036974 Shock HSDN C0518090 Frequency of pain question C0027873 Neuromyelitis optica HSDN C4085549 Dizziness C3813607 Infantile gastroesophageal reflux HSDN C3814530 Skin vesicle C0265965 Dyskeratosis congenita MalaCards|HPO C0030552 Paralysis partial C0342443 Adrenal cushing's syndrome MalaCards C1963065 Apnea adverse event C0017178 Gastrointestinal diseases HSDN C0728710 Pupil constriction observed C0014877 Esotropia HSDN C4085210 Usual severity pain C0026703 Mucopolysaccharidoses HSDN C1549543 Administration method - pain C2219717 Menstrual periods stopped for over 6 months HSDN C2364111 Gustatory anesthesia C1257915 Intestinal polyposis HSDN C4084774 Have weight loss C0004623 Bacterial infections HSDN C0008033 Pain pleural C2973787 Coxiella burnetii infection MalaCards C4085548 Usual severity dizziness C0206255 Malaria vaccine HSDN C0747556 Pharyngitis recurrent C0034494 Rabies (disorder) OrphaNet|MalaCards C0018991 Paralysis one side of body C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0221263 Cafe au lait spot C2750460 Tsc2 angiomyolipomas, renal, modifier of HPO C0018681 Headache, cephalalgia C0520779 Human ehrlichial infection, sennetsu type MalaCards C3887638 Failure to thrive in infant C0010709 Cyst HSDN C1000483 Genus anemia C0175692 Johanson-blizzard syndrome OrphaNet|HPO|MalaCards C0020578 Hyperventilate C0020651 Hypotension, orthostatic HSDN C1565249 Limitation, mobility C0004364 Autoimmune diseases HSDN C4085210 Usual severity pain C0752242 Limitus, hallux HSDN C1999266 Depression adverse event C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C0040822 D tremors C0206603 Circoviridae infection HSDN C0010038 Corneal opacity disorder C0026709 Mucopolysaccharidosis vi MalaCards C0024312 Lymphocytopenia C3809768 Immunodeficiency 13 MalaCards C4084725 Usual severity cough C0022107 Irritable mood HSDN C0012569 Double vision C0037379 Snake bite HSDN C4084774 Have weight loss C0031345 Pharyngeal diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0521170 Fracture due to osteoporosis HSDN C3887873 Hearing loss C0040034 Thrombocytopenia HSDN C1549543 Administration method - pain C0036271 Scalp dermatoses HSDN C4084768 Usual severity vomiting C0024636 Malocclusion HSDN C4084769 Vomiting frequency C0022951 Lactose intolerance HSDN C0008031 Pain chest C2711266 Infection by anisakis larva HSDN C0020580 Decreased sensation C0012979 Canine disease HSDN C3898969 Have been vomiting C0162576 Anisakiasis HSDN C3146279 Coma C0004377 Automatism HSDN C0036572 Convulsion C0036983 Septic shock HSDN C3463815 Feel fatigue C0008350 Cholelithiasis HSDN C4085862 Bothered by nausea C0004352 Autistic disorder HSDN C0018991 Paralysis one side of body C0030470 Paranasal sinus neoplasms HSDN C0018784 Deafness sensorineural C0035921 Congenital rubella syndrome OrphaNet|MalaCards C0851578 Disorder sleep C0021831 Intestinal diseases HSDN C0030193 Sense of pain C0751651 Mitochondrial diseases HSDN C0557874 Global developmental delay C2749873 Chromosome 3q29 duplication syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C0040592 Trachoma HSDN C0152459 Striae C1414542 Fbn1 gene HSDN C0018681 Headache, cephalalgia C0022521 Kartagener syndrome HPO|UMLS C0009763 Conjunctiva inflammation C0851907 Coccidioides; infection MalaCards C0020673 Hypothermia (central) (local) C1962979 Burn adverse event HSDN C1321324 Bruns nystagmus C0027651 Tumor UMLS C0039870 Leanness C0011849 Diabetes mellitus HSDN C0022346 Yellow skin C0043251 Wounds and injuries HSDN C4084767 Bothered by vomiting C0012691 Dislocations HSDN C0497247 Blood pressure elevation C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C1136321 Hiv-associated lipodystrophy syndrome HSDN C0029163 Hemorrhage mouth C0023418 Leukemia HSDN C4085862 Bothered by nausea C0025063 Mediastinal neoplasms HSDN C0003862 Pain joint C1956390 Cranial arteritis MalaCards C1253937 Pericardial effusion C0346303 Thyrotroph adenoma MalaCards C3146279 Coma C0021843 Intestinal obstruction HSDN C0004941 Behavioral symptoms C0032897 Prader-willi syndrome OrphaNet|MalaCards C1963064 Anxiety adverse event C1855606 Burton syndrome MalaCards C0027796 Neuralgias C2984289 Melanoma pathway HSDN C0037317 Sleep disturbance C0238027 Botulism, infantile OrphaNet|MalaCards C2984058 Have pain C0206660 Germinoma HSDN C4084767 Bothered by vomiting C4049994 Insulin resistance measurement HSDN C4042891 Sleep wake disorders C0021295 Infant, premature, diseases HSDN C2096293 Ent surgical result ear vertigo C0013364 Dysautonomia, familial HSDN C1963093 Dizziness adverse event C0004303 Auditory disease, central HSDN C0010200 Cough symptom C0023869 Lithiasis HSDN C0001825 Agraphia C1579931 Depressed - symptom HSDN C3829611 Nausea frequency C0015457 Expression facial HSDN C2984058 Have pain C0015806 Femur neck fracture HSDN C0018772 Deafness C4015038 Myasthenic syndrome, congenital, 7, presynaptic MalaCards C0030193 Sense of pain C0410249 Myalgias viral UMLS C1963087 Constipation adverse event C0004275 Attitude health HSDN C0020458 Hyperhydrosis C2751683 Hirschsprung disease ganglioneuroblastoma OrphaNet|MalaCards C0008031 Pain chest C0041326 Pleural tuberculosis HSDN C0349506 Sun sensitivity C2713347 7-dehydrocholesterol reductase deficiency OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0018799 Heart diseases HSDN C3815497 Cough C1565489 Renal insufficiency HSDN C3887638 Failure to thrive in infant C0036508 Seborrheic dermatitis HSDN C0232466 Feeding difficulty C0022638 Ketosis MalaCards C3463815 Feel fatigue C0483368 Human anaplasmosis due to anaplasma phagocytophilum MalaCards C0022568 Inflammation corneal C0079154 Congenital nonbullous ichthyosiform erythroderma OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0016236 Flicker fusion HSDN C2911647 Weight gain adverse event C0343084 Capillary leak syndrome HSDN C0018772 Deafness C0019294 Hernia, inguinal HSDN C0151786 Weakness muscle C0035920 Rubella HSDN C2203646 Jaundice C0236969 Substance-related disorders HSDN C0518090 Frequency of pain question C0002957 Anger HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0700327 Clinical findings relating to memory HSDN C4085210 Usual severity pain C0023761 Lip neoplasms HSDN C0853986 Lymphocytes decreased C1851970 Dyskeratosis congenita, autosomal dominant MalaCards|HPO C1963184 Nystagmus adverse event C0206307 Canavan disease MalaCards|HPO C4084802 Usual severity diarrhea C0023530 Leukopenia HSDN C0497406 Over weight C0220847 C hepatitis virus HSDN C0009806 Constipate C0006118 Brain neoplasms HSDN C0151740 Intracranial hypertension C0162309 Adrenoleukodystrophy OrphaNet|MalaCards C0000737 Abdomen pain C1332987 Childhood choriocarcinoma of ovary UMLS C0042798 Vision dim C0042909 Vitreous hemorrhage HSDN C4084802 Usual severity diarrhea C0031542 Phlebitis HSDN C0973461 Dysphasia C1838630 Dysphasia, familial developmental OrphaNet|MalaCards C3641756 Have diarrhea C0026847 Spinal muscular atrophy HSDN C1971624 Appetite absent C0043398 Yellow fever, urban MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0026705 Mucopolysaccharidosis ii HSDN C0242936 Center pain C4041080 Neurocognitive disorders HSDN C1549543 Administration method - pain C0039373 Tay-sachs disease HSDN C2919142 Short stature adverse event C1861456 Stiff skin syndrome MalaCards|HPO C0497406 Over weight C0032285 Pneumonia HSDN C0231791 In toe C0265210 Weaver syndrome MalaCards|HPO C0027066 Myoclonic jerking C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C1557397 Adverse event associated with pain C0023787 Lipodystrophy HSDN C1963249 Tinnitus adverse event C0556520 Psychological desensitization HSDN C4042891 Sleep wake disorders C0009088 Cluster headache HSDN C0013395 Indigestion C0024904 Mastoiditis HSDN C0030193 Sense of pain C0403447 Chronic kidney insufficiency HSDN C4084724 Usual severity constipation C0007138 Carcinoma, transitional cell HSDN C0027066 Myoclonic jerking C3715049 Ceroid lipofuscinosis, neuronal, 13 UMLS C3541349 Syncope C0752347 Lewy body disease HSDN C0015469 Facial paralysis C1850746 Carey-fineman-ziter syndrome OrphaNet C0023380 Lethargy C0043397 Yellow fever, jungle MalaCards C0917816 Deficiency mental C4015316 Epileptic encephalopathy, early infantile, 27 MalaCards C0039870 Leanness C0030567 Parkinson disease HSDN C0460137 Push down or depress C0334123 Histiocytosis, lipoid MalaCards C0151786 Weakness muscle C0035334 Retinitis pigmentosa HSDN C0000737 Abdomen pain C0018802 Congestive heart failure HSDN C0015469 Facial paralysis C0032965 Pregnancy complications, infectious HSDN C0042963 Symptoms vomiting C1548777 Specimen reject reason - hemolysis HSDN C0002622 Amnesias C0002989 Epithelioid hemangioma of skin HSDN C1069915 Vertigo C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0010674 Cystic fibrosis HSDN C4085211 Pain distress question C0030790 Pelvis infection HSDN C0152459 Striae C0027577 Nelson syndrome OrphaNet|MalaCards C4084802 Usual severity diarrhea C0041974 Urethral stricture HSDN C4085210 Usual severity pain C1321581 Bezoar disorder HSDN C0013604 Edematous C0036330 Schistosomiasis mansoni HSDN C4085211 Pain distress question C0038166 Staphylococcal skin infections HSDN C0221263 Cafe au lait spot C3150675 Chromosome 15q24 duplication syndrome HPO C0042571 Vertigo subjective C4049994 Insulin resistance measurement HSDN C0005745 Blepharoptosis C0022541 Kearns-sayre syndrome MalaCards C0018991 Paralysis one side of body C0033860 Psoriasis HSDN C0085636 Light sensitivity C0009774 Conjunctivitis viral MalaCards C2984058 Have pain C0030767 Grouping peer HSDN C4084788 Have dizziness C0206504 Tympanic membrane perforation HSDN C0010200 Cough symptom C0153564 Pulmonary kaposi sarcoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0009938 Bruising HSDN C0018772 Deafness C3850155 Congenital microtia HSDN C0030193 Sense of pain C0020459 Hyperinsulinism HSDN C0030552 Paralysis partial C0035372 Rett syndrome MalaCards|HPO C0848203 Male pelvic pain C0007097 Carcinomas HSDN C0278152 Hemifacial spasms C0020492 Hyperostosis HSDN C3898969 Have been vomiting C0342793 Malonic aciduria MalaCards|HPO C0018808 Murmur C2984289 Melanoma pathway HSDN C1963091 Diarrhea adverse event C0021400 Influenza HSDN C3641755 Have constipation C0036983 Septic shock HSDN C0000737 Abdomen pain C0020303 Hydropneumothorax HSDN C4084784 Diarrhea C0026936 Mycoplasma infections HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162429 Malnutrition HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024473 Magnesium deficiency HSDN C1279888 Proteinuria of undiagnosed cause C0333497 Segmental glomerulosclerosis HPO C1557397 Adverse event associated with pain C0242231 Coronary stenosis HSDN C0018681 Headache, cephalalgia C0021390 Inflammatory bowel diseases HSDN C0521632 Penis irritation C0080276 Disorder of the genitourinary system UMLS C4084767 Bothered by vomiting C0036690 Septicemia HSDN C4084775 Usual severity weight loss C0346407 Pancreatic polypeptide-oma MalaCards C3463815 Feel fatigue C0003869 Arthritis, infectious HSDN C0042024 Urine incontinence C0018801 Heart failure HSDN C0522224 Palsied C0031142 Peritoneal diseases HSDN C4085211 Pain distress question C0037824 Intelligibilities, speech HSDN C3539896 Pelvic pain occurs with urination C0272414 Displaced spleen HSDN C0042024 Urine incontinence C1846980 Senior-loken syndrome 3 MalaCards C0518090 Frequency of pain question C0010246 Coxsackievirus infections HSDN C0349588 Stature short C1865639 Gracile bone dysplasia MalaCards|HPO C4084766 Vomiting C1449842 Pseudohypoaldosteronism, type i, autosomal dominant HPO C0011991 Loose stools C0004610 Bacteremia HSDN C4085549 Dizziness C0001430 Adenoma HSDN C0234146 Absent reflex C0270724 Infantile neuroaxonal dystrophy HPO C0018681 Headache, cephalalgia C0483368 Human anaplasmosis due to anaplasma phagocytophilum MalaCards C1557397 Adverse event associated with pain C0032226 Pleural diseases HSDN C4084784 Diarrhea C0031117 Peripheral neuropathy HSDN C0027497 Queasy C0333355 Inflammatory disease of mucous membrane HSDN C0152459 Striae C0269680 Pruritic urticarial papules plaque pregnancy MalaCards C0036572 Convulsion C1854465 Tuberous sclerosis 1 (disorder) UMLS C4085222 Nausea C0028796 Dermatitis, occupational HSDN C4085210 Usual severity pain C0079631 Interdisciplinary communication HSDN C0917816 Deficiency mental C1859878 Alopecia-mental retardation syndrome 1 MalaCards C0002962 Angina C0032019 Pituitary neoplasms HSDN C0557874 Global developmental delay C0268611 Arakawa syndrome 2 MalaCards C1549543 Administration method - pain C0023798 Lipoma HSDN C1963180 Neck pain adverse event C0021368 Inflammation HSDN C0424755 Fever symptoms C0036271 Scalp dermatoses HSDN C0014724 Burping C0013299 Duodenogastric reflux HSDN C0271215 Blindness legal C0268632 Homocarnosinosis MalaCards C0040034 Thrombocytopenia C0023381 Letterer-siwe disease MalaCards C1963091 Diarrhea adverse event C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C3641755 Have constipation C0037579 Soft tissue neoplasms HSDN C0231528 Muscle pain generalized C0035288 Reticuloendotheliosis, x-linked MalaCards C0009460 Communication impairment C1837218 Cleft palate, isolated HSDN C0020578 Hyperventilate C1962983 Cataract adverse event HSDN C0034933 Abnormal reflexes C0020097 Htlv-i infections HSDN C3463815 Feel fatigue C0040761 Transposition of great vessels HSDN C0018777 Deafness, conductive C2931817 Chromosome 2q37 deletion syndrome MalaCards|HPO C1535893 Orthostatic intolerance C0039239 Sinus tachycardia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0302497 Retrobulbar haemorrhage HSDN C4085862 Bothered by nausea C0393735 Headache disorders HSDN C0426579 Anorexia symptom C0031090 Periodontal diseases HSDN C0231528 Muscle pain generalized C4015067 Autoinflammation with infantile enterocolitis MalaCards|UMLS C0424755 Fever symptoms C0011265 Presenile dementia HSDN C0004134 Dyssynergia C0342613 Danish type familial amyloid cardiomyopathy MalaCards C0557874 Global developmental delay C1837713 Joubert syndrome 3 MalaCards C0043094 Weight gain C4050613 Anxiety scale (basc-2) HSDN C0007758 Cerebellar ataxia C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C1557397 Adverse event associated with pain C0007772 Intracranial arteriovenous malformation HSDN C0036572 Convulsion C1865644 Plantar lipomatosis, unusual facies, and developmental delay MalaCards|HPO C0002962 Angina C0029182 Orbit (eye disorders) HSDN C0042024 Urine incontinence C1527336 Sjogren's syndrome HSDN C1963281 Vomiting adverse event C0079744 Diffuse large b-cell lymphoma HSDN C0042025 Urinary incontinence stress C1962958 Hematoma adverse event HSDN C1963071 Back pain adverse event C0019069 Hemophilia a HSDN C0030193 Sense of pain C0023860 Listeriosis HSDN C2984058 Have pain C0150277 Meditations HSDN C0014591 Bleeding nose C0472803 Hypodysfibrinogenemia MalaCards C0034933 Abnormal reflexes C0151740 Intracranial hypertension HSDN C1549543 Administration method - pain C0085082 Fungemia HSDN C3539023 Pelvic pain increasing in frequency C0262655 Recurrent urinary tract infection HSDN C4084921 Usual severity itching C0030757 Pediculus capitis infestation DiseaseOntology C0242936 Center pain C1415701 Hprt1 gene HSDN C0151786 Weakness muscle C0003469 Anxiety disorders HSDN C0019079 Bloody sputum C0002871 Anemia HSDN C0851578 Disorder sleep C0872996 Q fever vaccine HSDN C1963281 Vomiting adverse event C0016542 Foreign body HSDN C0017181 Gastrointestinal bleed C0024788 Green monkey virus disease OrphaNet|MalaCards C0034150 Skin purpura C0473583 Nevus elasticus HSDN C0013428 Painful urination C0022667 Papillary necrosis HSDN C0557874 Global developmental delay C0265354 Charge syndrome MalaCards C0016927 Gag reflex C0038454 Cerebrovascular accident HSDN C0013404 Respiratory difficulty C0854988 Adenocarcinoma of lung, stage iv UMLS C0240715 Perineal lump C0347436 Lipoma of perineum UMLS C1549543 Administration method - pain C0085693 Acute appendicitis nos (disorder) MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0002991 Cutaneous fibrous histiocytoma HSDN C0424755 Fever symptoms C2239176 Liver carcinoma MalaCards|HSDN C0020455 Hypergammaglobulinemia C0085652 Pyoderma gangrenosum OrphaNet|HSDN|MalaCards C1963077 Bone pain adverse event C0263628 Tumoral calcinosis OrphaNet|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0853697 Neutrophil count decreased HSDN C0348588 Other forms of angina pectoris C0003850 Arteriosclerosis UMLS C0039070 Collapse fleeting C0243002 Tricuspid atresia HSDN C3812171 Bradycardia by ecg finding C0030528 Paratyphoid fever DiseaseOntology|MalaCards C0522224 Palsied C0161408 Cranial nerve vii injuries HSDN C0155552 Hearing loss mixed C1849661 Acrootoocular syndrome MalaCards C3641755 Have constipation C1412397 Ancr gene HPO C2911645 Weight loss adverse event C0022665 Kidney neoplasm HSDN C0151786 Weakness muscle C2609414 Acute kidney injury HSDN C1565249 Limitation, mobility C0024117 Chronic obstructive airway disease HSDN C0027796 Neuralgias C0039494 Temporomandibular joint disorders HSDN C0413252 Hypothermia due to exposure C0027932 Neurotic disorders HSDN C1971624 Appetite absent C0262584 Carcinoma, small cell HSDN C0151786 Weakness muscle C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C0424755 Fever symptoms C1861980 Prenatal cortical hyperostosis, lethal HPO C0013404 Respiratory difficulty C0175816 Cold hemagglutinin disease OrphaNet C0018772 Deafness C1853473 Paget disease of bone 4 MalaCards C0086439 Activity decreased C0035053 Spontaneous remission HSDN C1549543 Administration method - pain C0013533 Echovirus infections HSDN C0012569 Double vision C0009241 Cognition disorders HSDN C0028738 Nystagmus C3496228 Leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia MalaCards C4084802 Usual severity diarrhea C0032897 Prader-willi syndrome HSDN C0028961 Urine output decreased C0027720 Nephrosis HSDN C0036572 Convulsion C0272199 Familial hemophagocytic lymphocytosis MalaCards|UMLS C0036572 Convulsion C1332949 Childhood brain meningioma UMLS C0728710 Pupil constriction observed C0024440 Macular edema, cystoid HSDN C0043144 Wheeze C0035235 Respiratory syncytial virus infections MalaCards C0151889 Reflexes tendon increased C1850510 Sialidosis, type i HPO C0018524 Hallucinate C1847640 Kufor-rakeb syndrome MalaCards|HPO C0038002 Spleen enlargement C0007932 Chagas' disease + no organ inv MalaCards C0018681 Headache, cephalalgia C0041466 Typhoid fever DiseaseOntology|OrphaNet|MalaCards C0023014 Developmental disorder language C1556682 Adverse event associated with infection HSDN C4084768 Usual severity vomiting C0020625 Hyponatremia HSDN C0035232 Diaphragmatic paralysis C0039614 Tetanus HSDN C0011168 Disorder deglutition C0030521 Parathyroid neoplasms MalaCards C2237041 Shox gene with short stature C0796055 Mercaptolactate-cysteine disulfiduria OrphaNet|MalaCards C0011991 Loose stools C0038271 Stereotyped behavior HSDN C0003862 Pain joint C3672366 Kozlowski celermajer tink syndrome MalaCards C1565249 Limitation, mobility C1956346 Coronary artery disease HSDN C0042571 Vertigo subjective C0009375 Colonic neoplasms HSDN C0043094 Weight gain C2240374 Eosinophil count raised HSDN C0037199 Sinus infection C0472813 X-linked agammaglobulinemia with growth hormone deficiency HPO C0751837 Gait ataxic C1832466 Capos syndrome HPO|UMLS C4084766 Vomiting C0004935 Animal ethology HSDN C2029884 Hearing loss by exam C0796117 Pitt syndrome MalaCards C0022408 Disorder joint C0432215 Progressive pseudorheumatoid dysplasia HPO C4084802 Usual severity diarrhea C3489393 Hiatal hernia HSDN C2984057 Have nausea C0020545 Hypertension, renovascular HSDN C1963281 Vomiting adverse event C1621920 Intermediate maple syrup urine disease HPO C3463815 Feel fatigue C0032273 Pneumoconiosis HSDN C4084727 Cough frequency C0008073 Developmental disabilities HSDN C0024031 Back pain lower back C0011581 Depressive disorder HSDN C0015672 Decreased energy C0027902 Neuropsychological diagnosis HSDN C0030200 Intractable pain C0018790 Cardiac arrest HSDN C2315100 Pediatric failure to thrive C0014544 Epilepsy HSDN C3815497 Cough C3887662 Intraspinal neoplasm HSDN C0015468 Face pain C0029423 Cartilaginous exostosis HSDN C0007758 Cerebellar ataxia C0152164 Cyclical vomiting syndrome (disorder) MalaCards C2037140 Sudden loss of vision in upper half of visual field in left eye C0018979 Hemianopsia UMLS C0424755 Fever symptoms C0003486 Aortic aneurysm HSDN C2242996 Tingling C0027531 Neck injury HSDN C3898969 Have been vomiting C0349653 Congenital disorder of glycosylation type 1a MalaCards|HPO C0015468 Face pain C0024720 Anxiety scale, manifest HSDN C2984058 Have pain C0003950 Ascariasis HSDN C0917816 Deficiency mental C1847352 Polymicrogyria, bilateral frontoparietal MalaCards|HPO C1069915 Vertigo C0597109 Nurse's role HSDN C0424755 Fever symptoms C0333641 Atrophic HSDN C0042571 Vertigo subjective C0524910 Hepatitis c, chronic HSDN C1963086 Confusion adverse event C0000768 Congenital abnormality HSDN C0004134 Dyssynergia C0027814 Neuritis, autoimmune, experimental HSDN C4084727 Cough frequency C3178892 Disease, pelvic floor HSDN C0020672 Body temperature decreased C1457883 Aggressive reaction HSDN C0019079 Bloody sputum C1290398 Cerebral arterial aneurysm HSDN C0042963 Symptoms vomiting C0021845 Intestinal perforation HSDN C0000737 Abdomen pain C1333758 Gallbladder signet ring cell carcinoma UMLS C3898969 Have been vomiting C2945767 Childhood liver cancer MalaCards C1384666 Decreased hearing C0162666 Mitochondrial encephalomyopathies HSDN C0018784 Deafness sensorineural C0023434 Chronic lymphocytic leukemia HSDN C3641756 Have diarrhea C0039483 Giant cell arteritis HSDN C4085317 Diarrhea frequency C0022570 Keratitis dentritic HSDN C0518090 Frequency of pain question C0011175 Dehydration HSDN C0497406 Over weight C0015579 Family characteristics HSDN C1549543 Administration method - pain C0014358 Enterocolitis, pseudomembranous HSDN C4084769 Vomiting frequency C0015802 Femur fracture HSDN C1963093 Dizziness adverse event C0011570 Mental depression HSDN C0004604 Pain back C0080178 Spina bifida HSDN C1549543 Administration method - pain C0042267 Vaginitis HSDN C4084767 Bothered by vomiting C1261128 Progeria-like syndrome MalaCards C0018681 Headache, cephalalgia C0085438 Fungal meningitis, nos HSDN C0011570 Monopolar depression C3160718 Parkinson disease, late-onset MalaCards|HPO C0151825 Ostalgia C0265309 Leri-weill dyschondrosteosis MalaCards C0040460 Dental pain C0018799 Heart diseases HSDN C1962957 Flushing adverse event C0206728 Plexiform neurofibroma HSDN C0426579 Anorexia symptom C0030920 Peptic ulcer HSDN C0282005 Scrotum swelling C0022661 Kidney failure, chronic UMLS C0042384 Vasculitis, nonspecific C4049638 Cutaneous small vessel vasculitis MalaCards C0016927 Gag reflex C0007789 Cerebral palsy HSDN C0026826 High muscle tone C2828721 Spastic paraplegia 46, autosomal recessive MalaCards C0522224 Palsied C0919727 Anaesthesia awareness HSDN C0518090 Frequency of pain question C0751931 Femoral lesion nerve HSDN C2096293 Ent surgical result ear vertigo C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) MalaCards C3665492 Pigmentations C0032197 Platelet storage pool deficiency MalaCards C0518090 Frequency of pain question C0018206 Granulosa cell tumor HSDN C0039070 Collapse fleeting C0010709 Cyst HSDN C0005745 Blepharoptosis C1851878 Orofacial cleft 8 MalaCards|HPO C4084724 Usual severity constipation C0041296 Tuberculosis HSDN C0017181 Gastrointestinal bleed C0158683 Polycystic liver disease MalaCards|HPO C0024902 Mastodynia C0033578 Prostatic neoplasms HSDN C0042928 Paralysis vocal cord C0007279 Carotid body paraganglioma HSDN|HPO C0003862 Pain joint C1368355 Synostosis malformation HSDN C1557397 Adverse event associated with pain C0024899 Mastocytosis HSDN C1963063 Anorexia adverse event C0270858 Abdominal migraines MalaCards C0013604 Edematous C0856761 Budd-chiari syndrome HSDN C0028738 Nystagmus C0795949 Galloway mowat syndrome HPO C4084766 Vomiting C0019348 Herpes simplex infections HSDN C4084767 Bothered by vomiting C0011303 Demyelinating diseases HSDN C0018834 Brash C2677682 Rett syndrome, zappella variant HPO C3887873 Hearing loss C0025149 Medulloblastoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0206504 Tympanic membrane perforation HSDN C0518090 Frequency of pain question C0018553 Hamartoma syndrome, multiple HSDN C0851578 Disorder sleep C1963090 Dehydration adverse event HSDN C0851578 Disorder sleep C0033586 Failure, prosthesis HSDN C0086437 Joint hypermobility C3151069 Chromosome 17p13.1 deletion syndrome MalaCards C0043094 Weight gain C0206062 Lung diseases, interstitial HSDN C0015230 Exanthem C0857090 Patchy rash UMLS C0684343 Pseudophakia C0008521 Choroid diseases HSDN C4084723 Constipation C1548578 Location characteristic id - smoking HSDN C1963281 Vomiting adverse event C2240374 Eosinophil count raised HSDN C4085211 Pain distress question C0023761 Lip neoplasms HSDN C4084727 Cough frequency C0917875 Esophageal diverticulosis HSDN C4084784 Diarrhea C0008065 Childhood behavior HSDN C0241210 Speaking delay C0432268 Osteopathia striata cranial sclerosis MalaCards|HPO C0242936 Center pain C0023646 Lichen planus HSDN C4084775 Usual severity weight loss C0040948 Trichostrongyliasis HSDN C0474368 Childbirth pain C0006157 Breech presentation HSDN C0039070 Collapse fleeting C0028433 Nose neoplasms HSDN C4084802 Usual severity diarrhea C0085136 Central nervous system neoplasms HSDN C0027498 Nausea vomiting C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C2045680 Change in thought patterns C0554978 Racing thoughts UMLS C4085862 Bothered by nausea C0006309 Brucellosis HSDN C3274924 Have been coughing C0007194 Hypertrophic cardiomyopathy HSDN C3641756 Have diarrhea C0043208 Wolman disease HPO C1962972 Proteinuria adverse event C1842982 Focal segmental glomerulosclerosis 3, susceptibility to HPO C0032617 High urine output C0034186 Pyelonephritis HSDN C0000737 Abdomen pain C0041311 Tuberculosis, female genital HSDN C4085211 Pain distress question C0027873 Neuromyelitis optica HSDN C0349588 Stature short C1845892 Hprt deficiency, neurologic variant HPO C2700617 Irritation - emotion C3279885 Hereditary sensory and autonomic neuropathy type ie MalaCards C3641755 Have constipation C0025222 Melena HSDN C3641755 Have constipation C0005416 Biliary dyskinesia HSDN C0242936 Center pain C0007868 Cervical dysplasia HSDN C1279888 Proteinuria of undiagnosed cause C0035204 Respiration disorders HSDN C4085211 Pain distress question C0036875 Disorders of sex development HSDN C0018681 Headache, cephalalgia C3897759 Recurrent childhood anaplastic oligodendroglioma UMLS C0497406 Over weight C0403447 Chronic kidney insufficiency HSDN C0042420 Vasovagal episode C0007137 Squamous cell carcinoma HSDN C0030486 Extremity paralysis, lower C0599412 Lordosis [mating posture] HSDN C0042514 Ventricular tachycardia C2678476 Cardiomyopathy, dilated, 1y MalaCards|HPO C3463815 Feel fatigue C0032343 Poisoning HSDN C0036396 Sciatica C0009730 Spinal meningocele HSDN C0018524 Hallucinate C1258104 Diffuse scleroderma HSDN C0038506 Stutter C0037078 Language sign HSDN C4085211 Pain distress question C0206711 Pilomatrixoma HSDN C4084725 Usual severity cough C0021933 Intussusception HSDN C2242996 Tingling C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C0030193 Sense of pain C0019522 Adenoma, sweat gland HSDN C3887638 Failure to thrive in infant C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C1384666 Decreased hearing C3554001 Peroxisome biogenesis disorder 11b MalaCards C1549543 Administration method - pain C0085083 Ovarian hyperstimulation syndrome HSDN C2911645 Weight loss adverse event C0019061 Hemolytic-uremic syndrome HSDN C0233514 Behavior abnormal C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet C0018681 Headache, cephalalgia C0043168 Whooping cough due to unspecified organism HSDN C0013595 Eczematous dermatitis C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0851578 Disorder sleep C0015732 Fecal incontinence HSDN C0009806 Constipate C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C0007758 Cerebellar ataxia C0043020 Wallerian degeneration HSDN C0917814 Aphasia expressive C0393808 Charcot-marie-tooth disease, x-linked, 1 HPO C0151686 Growth retardation C0268147 Glycogen storage disease, type ix OrphaNet C0020672 Body temperature decreased C0043395 Yellow fever MalaCards C4084773 Bothered by weight gain C1535939 Pneumocystis jiroveci pneumonia HSDN C0042963 Symptoms vomiting C0021432 Infratentorial neoplasms HSDN C0013421 Dystonia C0080179 Vertebra fracture HSDN C0242936 Center pain C3463897 Hydatidiform mole, recurrent, 1 HSDN C0349588 Stature short C1868684 Ear, patella, short stature syndrome MalaCards C0027066 Myoclonic jerking C1263960 Diabetic coma HSDN C2984058 Have pain C0043241 Wound infection HSDN C3887873 Hearing loss C0019080 Hemorrhage HSDN C4084723 Constipation C0403555 Ochoa syndrome OrphaNet|HPO|MalaCards C1963064 Anxiety adverse event C0751156 Fraxa syndrome MalaCards|HPO C0042940 Disorder of voice C0024141 Lupus erythematosus, systemic HSDN C0019079 Bloody sputum C0023470 Myeloid leukemia HSDN C0033377 Caudal displacement C0265245 Nager syndrome OrphaNet|HPO|MalaCards C1963281 Vomiting adverse event C0023487 Acute promyelocytic leukemia HSDN C0221184 Hemianopsia bitemporal C0025286 Meningioma MalaCards C0040822 D tremors C0005686 Urinary bladder diseases HSDN C0043094 Weight gain C0033817 Pseudomonas infections HSDN C2984057 Have nausea C0038463 Strongyloides infection HSDN C0349588 Stature short C2930971 Acroosteolysis dominant type OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0042063 Urogenital abnormalities HSDN C1961131 Cough adverse event C0021400 Influenza DiseaseOntology|MalaCards C0011991 Loose stools C1443901 Intestinal botulism OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0004576 Babesiosis OrphaNet|MalaCards C4084793 Have hair loss C1851970 Dyskeratosis congenita, autosomal dominant MalaCards C0042571 Vertigo subjective C3150754 Glycogen storage disease xv MalaCards C0013604 Edematous C0042138 Uterine neoplasms HSDN C0027498 Nausea vomiting C2936917 Infantile polyarteritis MalaCards C2700617 Irritation - emotion C0040156 Thyrotoxicosis MalaCards C0043144 Wheeze C0264412 Extrinsic asthma - no status UMLS C0018772 Deafness C0030567 Parkinson disease HSDN C1961131 Cough adverse event C0040136 Thyroid neoplasm HSDN C0026838 Spasticity muscle C4014343 Mental retardation, autosomal recessive 42 MalaCards C0557874 Global developmental delay C3554235 Joubert syndrome 20 MalaCards C1963170 Hypothermia adverse event C0005586 Bipolar disorder HSDN C4084724 Usual severity constipation C0235387 Porphyria type syndrome OrphaNet C3541349 Syncope C0002871 Anemia HSDN C2911647 Weight gain adverse event C0041582 Ulcer HSDN C4084774 Have weight loss C0034530 Injury radiation HSDN C2315100 Pediatric failure to thrive C0002514 Amino acid metabolism, inborn errors HSDN C0039231 Heartbeats increased C0030421 Paraganglioma HPO C0349588 Stature short C0795942 Fitzsimmons-guilbert syndrome HPO C4084784 Diarrhea C1306577 Dies patient HSDN C3494358 Characteristic, prodromal C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084725 Usual severity cough C0997768 Glaucoma HSDN C0019214 Hepatosplenomegaly C1856304 Gsd iv, neuromuscular form, congenital MalaCards|HPO C1549543 Administration method - pain C0037198 Sinus thrombosis, intracranial HSDN C0013362 Dysarthrias C0393576 Chorea acanthocytosis syndrome OrphaNet|HSDN|HPO|MalaCards C0015300 Ocular proptosis C1862178 Cole carpenter syndrome OrphaNet|HPO|MalaCards C0026826 High muscle tone C0028303 Nondisjunction HSDN C0018524 Hallucinate C0338437 Neurocysticercosis HSDN C1549543 Administration method - pain C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C4084802 Usual severity diarrhea C0016952 Galactosemias MalaCards C0018772 Deafness C3280296 Microcephaly-capillary malformation syndrome MalaCards C0578994 Bad mouth taste C0234297 Taste disorder, primary UMLS C0036572 Convulsion C0011311 Dengue fever HSDN C1384666 Decreased hearing C3536984 Vitamin d-resistant rickets, x-linked MalaCards|HSDN|HPO C4085661 Usual severity nausea C0020523 Immediate hypersensitivity HSDN C4084769 Vomiting frequency C0010674 Cystic fibrosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0042485 Venous insufficiency HSDN C4020887 Photodysphoria C0036202 Sarcoidosis MalaCards C0018520 Breath odor C0031345 Pharyngeal diseases HSDN C1963091 Diarrhea adverse event C0042162 Uveal neoplasms HSDN C2984058 Have pain C0243050 Cardiovascular abnormalities HSDN C0151786 Weakness muscle C1959582 Pten hamartoma tumor syndrome MalaCards C2237041 Shox gene with short stature C3554446 Brachydactyly, type a1, c MalaCards C4084767 Bothered by vomiting C0344479 Spinal cord myelodysplasia HSDN C0013911 Emaciate C1704436 Peripheral arterial diseases HSDN C1963242 Stomach pain adverse event C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C0027796 Neuralgias C0034628 Radius fracture HSDN C0004604 Pain back C0012817 Diverticulum HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0015618 Families therapy HSDN C0423823 Nail thinness C0587248 Costello syndrome (disorder) MalaCards|HPO C0018784 Deafness sensorineural C2749346 Refsum disease, adult, 2 MalaCards|HPO C2129343 Unreasonable fear of natural environment C0558207 Brontophobia UMLS C1963281 Vomiting adverse event C0004659 Bacteriuria HSDN C0034150 Skin purpura C3150741 Immunodeficiency, common variable, 6 MalaCards|HPO C0018772 Deafness C0022658 Kidney diseases HSDN C4084769 Vomiting frequency C0010417 Cryptorchidism HSDN C1519353 Skin eruption papular C1274700 Postmenopausal frontal fibrosing alopecia MalaCards C0015672 Decreased energy C0206172 Diabetic foot HSDN C0184567 Pain acute C0221069 Anterior spinal artery syndrome HSDN C0011570 Monopolar depression C0751706 Primary progressive nonfluent aphasia OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0003950 Ascariasis HSDN C0034933 Abnormal reflexes C0037019 Shy-drager syndrome HSDN C1962972 Proteinuria adverse event C3812171 Bradycardia by ecg finding HSDN C0007758 Cerebellar ataxia C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2911645 Weight loss adverse event C2347126 Microscopic polyarteritis HSDN C4085211 Pain distress question C1963119 Stomach ulcer adverse event HSDN C4084766 Vomiting C1864499 Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss HPO C3163620 Hypotension adverse event C1840365 King denborough syndrome HPO C0019825 Voice hoarseness C1860315 Whispering dysphonia, hereditary MalaCards C1549543 Administration method - pain C0025521 Inborn errors of metabolism HSDN C2911645 Weight loss adverse event C0002726 Amyloidosis HSDN C0026838 Spasticity muscle C1850386 Giant axonal neuropathy 1 MalaCards C1279888 Proteinuria of undiagnosed cause C0022116 Ischemia HSDN C0151786 Weakness muscle C2930798 Alexanders leukodystrophy MalaCards C0242936 Center pain C0031030 Periapical periodontitis HSDN C2032395 Pelvic pain on the left C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3274924 Have been coughing C2931785 Juvenile dermatomyositis MalaCards C4084769 Vomiting frequency C0027659 Neoplasms, experimental HSDN C0424755 Fever symptoms C1540912 Hypereosinophilic syndrome HSDN C4085210 Usual severity pain C0027726 Nephrotic syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014901 Aesthetic HSDN C1963086 Confusion adverse event C0002886 Anemia, macrocytic HSDN C0751837 Gait ataxic C4015436 Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus MalaCards|UMLS C0018681 Headache, cephalalgia C4086151 Childhood anaplastic ependymoma UMLS C0237326 Defecation pain C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0332563 Papulae C0346010 Multiple fibrofolliculomas OrphaNet|HPO|MalaCards C0020538 Hbp C0265915 Congenital stenosis, pulmonary veins OrphaNet|MalaCards C3146279 Coma C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C3274920 Have shortness of breath question C0155877 Allergic asthma DiseaseOntology C0042024 Urine incontinence C0010417 Cryptorchidism HSDN C0151825 Ostalgia C0432292 Familial expansile osteolysis HPO C1963091 Diarrhea adverse event C1704272 Benign prostatic hyperplasia HSDN C0036572 Convulsion C0006287 Bronchopulmonary dysplasia HSDN C2024893 Cardiovascular surgery result: fatigue C0406645 Amyopathic dermatomyositis MalaCards C0039070 Collapse fleeting C0038454 Cerebrovascular accident HSDN|UMLS C0036572 Convulsion C1531647 Cerebral ventriculomegaly HPO C3665386 Abnormal vision C0751383 Juvenile neuronal ceroid lipofuscinosis MalaCards C0009676 Confusion state C0155862 Streptococcal pneumonia HSDN C0038002 Spleen enlargement C1318518 Infantile malignant osteopetrosis OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C1514428 Primary peritoneal carcinoma MalaCards C3463815 Feel fatigue C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) MalaCards C3146279 Coma C0023903 Liver neoplasms HSDN C0010200 Cough symptom C0314657 Genetic predisposition HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019069 Hemophilia a HSDN C4084768 Usual severity vomiting C0014121 Bacterial endocarditis HSDN C4085317 Diarrhea frequency C0206247 Amyloid neuropathies MalaCards C0151889 Reflexes tendon increased C0024408 Machado-joseph disease OrphaNet|MalaCards C4085222 Nausea C0014849 Esophageal and gastric varices HSDN C0000737 Abdomen pain C1963119 Stomach ulcer adverse event HSDN C0033774 Skin pruritus C0268398 Familial lichen amyloidosis MalaCards|HPO C0007814 Cerebrospinal fluid otorrhea C0005940 Bone diseases HSDN C1860844 Sparse, thin hair C0021171 Bloch sulzberger syndrome MalaCards C3641756 Have diarrhea C0005941 Bone diseases, developmental HSDN C1549543 Administration method - pain C0037361 Olfactory sense HSDN C0349588 Stature short C2931506 Stern lubinsky durrie syndrome MalaCards C3887873 Hearing loss C0007784 Cerebral hemisphere hemorrhage HSDN C2029884 Hearing loss by exam C0012691 Dislocations HSDN C4085549 Dizziness C0019163 Hepatitis b HSDN C0011991 Loose stools C3814778 Hemolytic index HSDN C0344428 Ventricular tachycardia by ecg finding C1858379 Arrhythmogenic right ventricular dysplasia, familial, 5 (disorder) HPO C0018784 Deafness sensorineural C1962986 Glaucoma adverse event HSDN C3539893 Pelvic pain occurs with intercourse C2586211 Thrombosis of blood vessel HSDN C0151818 Opisthotonos C0023374 Lesch-nyhan syndrome MalaCards|HPO|UMLS C0007758 Cerebellar ataxia C0684324 Deficiency of phosphoglycerate kinase MalaCards C2076647 Infraorbital eye pain right C1400948 Infraorbital; pain UMLS C2242996 Tingling C0011881 Diabetic nephropathy HSDN C0015672 Decreased energy C0008066 Child behavior disorders HSDN C4084726 Distress cough C0019114 Hemosiderosis HSDN C0085642 Asphyxia reticularis C0011609 Drug eruptions HSDN C2919142 Short stature adverse event C3809877 Schaaf-yang syndrome MalaCards C4085862 Bothered by nausea C0028738 Nystagmus HSDN C0003910 Articulation disorder C3542413 Cdisc adas-cog - comprehension HSDN C1962972 Proteinuria adverse event C0398641 Epstein syndrome (disorder) HPO C1549543 Administration method - pain C0005818 Blood platelet disorders HSDN C1963091 Diarrhea adverse event C0009377 Colon nos pseudo obstruction HSDN C0151889 Reflexes tendon increased C0346068 Cobb syndrome OrphaNet|MalaCards C0011991 Loose stools C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0332563 Papulae C1866983 Scleroderma, familial progressive MalaCards C4084784 Diarrhea C2020541 Strabismus HSDN C0030193 Sense of pain C1332613 Adenoacanthoma of breast UMLS C4084726 Distress cough C0010340 Critical illness HSDN C0013404 Respiratory difficulty C3541306 Plasmodium measurement HSDN C0424755 Fever symptoms C0344423 Atrial flutter by ecg finding HSDN C0013604 Edematous C1850674 Minicore myopathy with external ophthalmoplegia (disorder) MalaCards C4085210 Usual severity pain C0027531 Neck injury HSDN C0042024 Urine incontinence C0162309 Adrenoleukodystrophy MalaCards|HPO C1549543 Administration method - pain C1704212 Embolism embolus HSDN C2096293 Ent surgical result ear vertigo C0003507 Aortic valve stenosis HSDN C0332563 Papulae C0018553 Hamartoma syndrome, multiple OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0023467 Leukemia, myelocytic, acute HSDN C0413252 Hypothermia due to exposure C0001580 Adolescent behavior HSDN C0522224 Palsied C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C0013911 Emaciate C0002726 Amyloidosis HSDN C0043094 Weight gain C0038013 Ankylosing spondylitis HSDN C4084784 Diarrhea C0001768 Agammaglobulinemia OrphaNet|MalaCards C4084769 Vomiting frequency C0019348 Herpes simplex infections HSDN C0086565 Liver function abnormal C0948441 Venoocclusive disease MalaCards C0424755 Fever symptoms C4042784 Feeding and eating disorders HSDN C0750937 Appendicular ataxia C1847416 Friedreich ataxia with retained reflexes HPO C1549543 Administration method - pain C0021141 Inappropriate adh syndrome HSDN C0011168 Disorder deglutition C2750536 Nemaline myopathy 3, with intranuclear rods HPO C4084767 Bothered by vomiting C0036946 Sheep--diseases HSDN C0013604 Edematous C0398775 Hereditary c1 esterase inhibitor deficiency - deficient factor MalaCards C1549543 Administration method - pain C1009209 Tinea HSDN C4084768 Usual severity vomiting C0011881 Diabetic nephropathy HSDN C3898969 Have been vomiting C0006434 Burn injury HSDN C1279888 Proteinuria of undiagnosed cause C0012644 Animal disease models HSDN C0003811 Cardiac rhythm disturbance C0031069 Familial mediterranean fever HPO C0007758 Cerebellar ataxia C1838979 Mitochondrial complex i deficiency MalaCards|HPO C0027066 Myoclonic jerking C0035410 Rhabdomyolysis HSDN C0349588 Stature short C3714796 Isolated somatotropin deficiency MalaCards C0744623 Head pain unilateral C0362076 Head problem UMLS C1963071 Back pain adverse event C0020255 Hydrocephalus HSDN C3887638 Failure to thrive in infant C0751267 Encephalopathy, subacute necrotizing, infantile MalaCards C0034150 Skin purpura C3150315 Aicardi-goutieres syndrome 1, autosomal dominant HPO C2203646 Jaundice C1552262 Nurse practitioner - family HSDN C3146279 Coma C0206255 Malaria vaccine HSDN C0178417 Anhedonia C0027932 Neurotic disorders HSDN C1557397 Adverse event associated with pain C0032064 Plague HSDN C0011991 Loose stools C0241910 Hepatitis, autoimmune HSDN C0020673 Hypothermia (central) (local) C0546884 Hypovolemia HSDN C0242936 Center pain C0037054 Sickle cell trait MalaCards|HSDN C4084769 Vomiting frequency C0025500 Mesothelioma HSDN C0004941 Behavioral symptoms C0041341 Tuberous sclerosis OrphaNet|HPO C4084767 Bothered by vomiting C0023903 Liver neoplasms HSDN C0012833 Dizzy C0220654 Meningeal carcinomatosis HSDN C0349588 Stature short C0796124 Proud syndrome HPO C4084724 Usual severity constipation C0079487 Helicobacter infections HSDN C4084774 Have weight loss C2239176 Liver carcinoma MalaCards C0036572 Convulsion C0595812 Fistula route HSDN C1961131 Cough adverse event C4050613 Anxiety scale (basc-2) HSDN C0033776 Pregnancy and pruritus C0451803 Dis of the skin and subcut tis comp preg childbrth puerp UMLS C0015672 Decreased energy C2981150 Uranostaphyloschisis HSDN C4084769 Vomiting frequency C0022822 Hunchback formed after birth HSDN C3641756 Have diarrhea C0034882 Rectal diseases HSDN C1961131 Cough adverse event C0025286 Meningioma HSDN C0035078 Failure kidney C1840451 Multicystic renal dysplasia, bilateral HPO C0018772 Deafness C0750929 Arnold-chiari malformation, type i MalaCards C3641756 Have diarrhea C0010072 Coronary thrombosis HSDN C0034124 Pupillary disorder C0007384 Cataplexy HSDN C2984058 Have pain C1299919 Enteric coccidiosis HSDN C4084784 Diarrhea C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C1837857 Deafness, autosomal recessive 35 MalaCards|HPO C0015799 Feminisation C0032787 Postoperative complications HSDN C0030193 Sense of pain C0032964 Pregnancy complications, hematologic HSDN C0235198 Disturbed mental concentration C1858680 Familial encephalopathy with neuroserpin inclusion bodies MalaCards C3665347 Vision impaired C0684324 Deficiency of phosphoglycerate kinase MalaCards C4084767 Bothered by vomiting C1691228 Cystic kidney diseases HSDN C2984057 Have nausea C0013289 Duodenal diseases HSDN C0033774 Skin pruritus C0149765 Psychogenic pruritis UMLS C0006370 Bulimia C0043065 Water electrolyte imbalance HSDN C0206146 Myocardial stunning C0027059 Myocarditis HSDN C0018965 Blood urine C0268381 Primary amyloidosis MalaCards C0019572 Hairiness C0037369 Smoking HSDN C3463815 Feel fatigue C0033054 Prenatal exposure delayed effects HSDN C0349588 Stature short C1848818 Thumb agenesis, short stature, and immunodeficiency MalaCards C0007758 Cerebellar ataxia C0266463 Lissencephaly HSDN C3274924 Have been coughing C0023895 Liver diseases HSDN C0000727 Abdomen acute C0036982 Shock, hemorrhagic HSDN C0000727 Abdomen acute C0038661 Suicide HSDN C3827868 Tachycardia by ecg finding C2936913 Porphyria, south african type HPO C0005745 Blepharoptosis C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C0242936 Center pain C0025312 Meningomyelocele HSDN C4085661 Usual severity nausea C0033871 Psychiatric status rating scales HSDN C1090821 Sepsis C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards|HPO C1557397 Adverse event associated with pain C0027430 Nasal polyps HSDN C0000737 Abdomen pain C0022876 Premature obstetric labor HSDN C2911645 Weight loss adverse event C0036202 Sarcoidosis OrphaNet|HSDN|HPO|MalaCards C2911647 Weight gain adverse event C0039231 Tachycardia HSDN C0022346 Yellow skin C0003873 Rheumatoid arthritis HSDN C0030554 Abnormal sensation C0453996 Tobacco smoking HSDN C0424755 Fever symptoms C0032966 Complication, neoplastic pregnancy HSDN C0917816 Deficiency mental C0265252 Coffin-lowry syndrome OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C1858084 Stickler syndrome, type ii (disorder) OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0042974 Von willebrand disease HSDN C4085317 Diarrhea frequency C0036421 Systemic scleroderma HSDN C3665492 Pigmentations C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0030193 Sense of pain C0013589 Ectromelia HSDN C0007758 Cerebellar ataxia C0014457 Eosinophilia HSDN C0011991 Loose stools C0003469 Anxiety disorders HSDN C2315100 Pediatric failure to thrive C2748440 Sensorineural deafness with mild renal dysfunction HPO C2984058 Have pain C0025472 Mesenteric vascular occlusion HSDN C4085210 Usual severity pain C0037052 Sick sinus syndrome HSDN C0015469 Facial paralysis C0006309 Brucellosis HSDN C4042891 Sleep wake disorders C0001580 Adolescent behavior HSDN C4085317 Diarrhea frequency C0039445 Hereditary hemorrhagic telangiectasia HSDN C0007758 Cerebellar ataxia C2677792 Riddle syndrome MalaCards|HPO C2029884 Hearing loss by exam C0025202 Melanoma HSDN C0015672 Decreased energy C0035412 Rhabdomyosarcoma HSDN C0349588 Stature short C2750787 Weill-marchesani-like syndrome HPO C0013604 Edematous C0004106 Astigmatism HSDN C2237041 Shox gene with short stature C1263846 Attention deficit hyperactivity disorder MalaCards C1263846 Attention deficit disorder with hyperactivity C1854465 Tuberous sclerosis 1 (disorder) HPO C0004310 Auditory disorder process C0007785 Cerebral infarction HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0032963 Pregnancy complications, cardiovascular HSDN C0151786 Weakness muscle C1704275 Pyomyositis HSDN C0086437 Joint hypermobility C1851710 Lateral meningocele syndrome MalaCards|HPO C1963252 Tremor adverse event C2751842 Parkinson disease 14, autosomal recessive MalaCards|HPO C0038002 Spleen enlargement C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C0344315 Mood depressed C2936779 Hydroxymethylbilane synthase deficiency MalaCards C2237041 Shox gene with short stature C3502492 Microcephaly with chorioretinopathy, autosomal recessive OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0043349 Xerophthalmia HSDN C0042798 Vision dim C1844776 Cone-rod dystrophy, x-linked, 1 MalaCards|HPO C0036572 Convulsion C0795914 Crome syndrome OrphaNet|MalaCards C0013604 Edematous C2717905 Hereditary angioedema types i and ii MalaCards C4084784 Diarrhea C0268181 Lactose intolerance, adult type HPO C1000483 Genus anemia C0268532 Deficiency of prolidase MalaCards|HPO C0004604 Pain back C0206663 Neuroectodermal tumor, primitive MalaCards|HSDN C0037199 Sinus infection C0018203 Chronic granulomatous disease OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0006663 Calcinosis HSDN C4042891 Sleep wake disorders C0030767 Grouping peer HSDN C0151786 Weakness muscle C1868619 Paramyotonia congenita without cold paralysis HPO C0010200 Cough symptom C0001144 Acne vulgaris HSDN C0019572 Hairiness C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4084766 Vomiting C0038587 Substance withdrawal syndrome HSDN C4084766 Vomiting C0030567 Parkinson disease HSDN C1549543 Administration method - pain C0017525 Giant cell tumors HSDN C2024893 Cardiovascular surgery result: fatigue C3244301 Coverage level - family HSDN C1963184 Nystagmus adverse event C1838180 Codas syndrome MalaCards|HPO C4084768 Usual severity vomiting C0014335 Enteritis HSDN C0015672 Decreased energy C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0018681 Headache, cephalalgia C0011633 Dermatomyositis HSDN C0344315 Mood depressed C1843851 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis HPO C0557874 Global developmental delay C0041341 Tuberous sclerosis OrphaNet|HPO C3665347 Vision impaired C0023521 Globoid cell leukodystrophy OrphaNet C4085862 Bothered by nausea C0009088 Cluster headache HSDN C4084769 Vomiting frequency C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C0018772 Deafness C0030297 Pancreatic neoplasm HSDN C0002962 Angina C0162316 Iron deficiency anemia HSDN C0518090 Frequency of pain question C0042267 Vaginitis HSDN C3898969 Have been vomiting C1420653 Tcn2 gene HPO C0033774 Skin pruritus C1090821 Sepsis (invertebrate) HSDN C2203646 Jaundice C1837218 Cleft palate, isolated HSDN C3809715 Epistaxis recurrent C0406702 Ectodermal dysplasia, hypohidrotic, autosomal recessive MalaCards C0000727 Abdomen acute C0027932 Neurotic disorders HSDN C2911647 Weight gain adverse event C0007621 Neoplastic cell transformation HSDN C2984058 Have pain C0524851 Neurodegenerative disorders HSDN C1963137 Hydrocephalus adverse event C1300257 Thanatophoric dysplasia, type 2 MalaCards|HPO C0241210 Speaking delay C3553582 Seckel syndrome 6 MalaCards C0039070 Collapse fleeting C1963138 Hypertension adverse event HSDN C3829611 Nausea frequency C0025149 Medulloblastoma HSDN C3887873 Hearing loss C1290398 Cerebral arterial aneurysm HSDN C0427055 Face weakness C0038454 Cerebrovascular accident UMLS C2032395 Pelvic pain on the left C0016548 Foreign body migration HSDN C1963077 Bone pain adverse event C0017205 Gaucher disease OrphaNet|MalaCards C1963071 Back pain adverse event C0002871 Anemia HSDN C0398650 Idiopathic thrombocytopenia purpura C0007222 Cardiovascular diseases HSDN C1963086 Confusion adverse event C0007761 Myoclonic cerebellar dyssynergia HSDN C1963087 Constipation adverse event C0003469 Anxiety disorders HSDN C1962956 Flatulence adverse event C0042961 Intestinal volvulus HSDN C0026826 High muscle tone C0018565 Acquired deformity of hand, nos HSDN C0857305 Thrombocytopenia purpura C0151744 Myocardial ischemia HSDN C4084802 Usual severity diarrhea C0560694 Bottles per feed HSDN C0042963 Symptoms vomiting C1518875 Pancreatic serous cystic neoplasm UMLS C0233407 Disorient C2931917 Alcoholic encephalopathy MalaCards C4085211 Pain distress question C0011303 Demyelinating diseases HSDN C4084766 Vomiting C0019911 Hookworm infections HSDN C1000483 Genus anemia C0035921 Congenital rubella syndrome OrphaNet|MalaCards C1549543 Administration method - pain C0020428 Hyperaldosteronism HSDN C0013378 Dysgensia C0041755 Adverse reaction to drug HSDN C0018681 Headache, cephalalgia C0035243 Respiratory tract infections HSDN C0033774 Skin pruritus C0032461 Polycythemia HSDN C0010200 Cough symptom C0014869 Peptic esophagitis HSDN C4085210 Usual severity pain C0424688 Small head HSDN C0020672 Body temperature decreased C0011884 Diabetic retinopathy HSDN C0024031 Back pain lower back C0233629 Thinking and speaking disturbances HSDN C2315100 Pediatric failure to thrive C0265219 Miller dieker syndrome MalaCards C4084768 Usual severity vomiting C1856403 Etfb deficiencies HPO C0013395 Indigestion C0036239 Satiety HSDN C1260880 Nasal drip C1333476 Ethmoid sinus schneiderian papilloma UMLS C4084723 Constipation C1956093 Paris-trousseau thrombocytopenia MalaCards C0014089 Functional encopresis C0037650 Somatoform disorder HSDN C0150055 Pain chronic C0030567 Parkinson disease HSDN C0917816 Deficiency mental C0796037 Martsolf syndrome OrphaNet|HPO|MalaCards C0034155 Thrombotic thrombocytopenic purpura C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C1963087 Constipation adverse event C0037933 Spinal diseases HSDN C4085222 Nausea C0001727 Afferent loop syndrome HSDN C0460137 Push down or depress C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C2919142 Short stature adverse event C0394006 Dysequilibrium syndrome OrphaNet|HPO C0003862 Pain joint C2745948 Hyalinosis, systemic HSDN C4084724 Usual severity constipation C3539495 Spastic paraplegia 54, autosomal recessive MalaCards C0015672 Decreased energy C0026269 Mitral valve stenosis HSDN C0028738 Nystagmus C3809592 Mitochondrial dna depletion syndrome 13 (encephalomyopathic type) MalaCards C1963137 Hydrocephalus adverse event C3554002 Pbd12a MalaCards C0003862 Pain joint C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C4084767 Bothered by vomiting C0041374 Tumor virus infections HSDN C4084775 Usual severity weight loss C2931638 Chromosome 8, monosomy 8p23 1 MalaCards C4085211 Pain distress question C0023794 Lipoidosis HSDN C0518090 Frequency of pain question C0034628 Radius fracture HSDN C1963064 Anxiety adverse event C0796249 Mental retardation, x linked 47 HPO C4084723 Constipation C3266898 Waardenburg syndrome OrphaNet|HPO C4084788 Have dizziness C0023890 Liver cirrhosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027661 Neoplasms, hormone-dependent HSDN C4084768 Usual severity vomiting C0085278 Antiphospholipid syndrome HSDN C4084723 Constipation C3888013 Hypnoses HSDN C0020672 Body temperature decreased C0027809 Neurilemmoma HSDN C4084775 Usual severity weight loss C0041327 Tuberculosis, pulmonary HSDN C0033790 Pseudobulbar palsy C2707011 Behavioral symptoms:-:point in time:^patient:- HSDN C0009676 Confusion state C0752155 Central nervous system vascular malformations HSDN C0023380 Lethargy C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0013911 Emaciate C0010691 Cystinuria HSDN C0917816 Deficiency mental C3810062 Congenital disorder of glycosylation, type iw MalaCards C0018784 Deafness sensorineural C0007784 Cerebral hemisphere hemorrhage HSDN C0010200 Cough symptom C0016169 Pathologic fistula HSDN C0042963 Symptoms vomiting C0268039 Ketoacidosis alcoholic UMLS C0004134 Dyssynergia C0004138 Ataxias, hereditary UMLS C0011168 Disorder deglutition C0750929 Arnold-chiari malformation, type i MalaCards C0233514 Behavior abnormal C0004943 Behcet syndrome MalaCards C3146279 Coma C0020542 Pulmonary hypertension HSDN C0030193 Sense of pain C0015395 Burn eye HSDN C0003962 Ascites C0037661 Somatostatinoma MalaCards C2055125 Temperature reported over 102 degrees fahrenheit C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C0917816 Deficiency mental C3809233 Noonan syndrome 8 MalaCards C0413252 Hypothermia due to exposure C0042018 Urinary calculi HSDN C0151786 Weakness muscle C1527336 Sjogren's syndrome HSDN C0578056 Pain of truncal structure C0423747 Dyspareunia deep UMLS C4085211 Pain distress question C0042900 Vitiligo HSDN C0004134 Dyssynergia C0027659 Neoplasms, experimental HSDN C4084784 Diarrhea C0014852 Esophageal diseases HSDN C0427190 Ataxia, truncal C3279716 Hypoacetylaspartia MalaCards C0036572 Convulsion C0265220 Pallister-hall syndrome MalaCards|HPO C0037315 Breathing disorder during sleeping C0001206 Acromegaly OrphaNet|HPO|MalaCards C0040034 Thrombocytopenia C1861451 Stormorken syndrome MalaCards C0234523 Apraxia, classic C0497327 Dementia HSDN C2242996 Tingling C0006436 Burning electric HSDN C4084768 Usual severity vomiting C0268573 Valinemia MalaCards C0015469 Facial paralysis C0751955 Brain infarction HSDN C0026821 Cramp C0012691 Dislocations HSDN C0013404 Respiratory difficulty C0037579 Soft tissue neoplasms HSDN C4084784 Diarrhea C2364172 Adherence to medication regime HSDN C0013421 Dystonia C3553788 Alternating hemiplegia of childhood 2 MalaCards C4085862 Bothered by nausea C3489393 Hiatal hernia HSDN C0041105 Jaw spasm C4084909 Depression subordinate domain HSDN C0008031 Pain chest C0001584 Adolescent psychology HSDN C3829611 Nausea frequency C0002878 Anemia, hemolytic HSDN C0242936 Center pain C0270857 Epilepsy, reflex HSDN C1963170 Hypothermia adverse event C0020488 Hypernatremia HSDN C0427068 Legs weakness C1858479 Spastic paraplegia 11, autosomal recessive MalaCards|HPO C2096293 Ent surgical result ear vertigo C0517555 Venous thrombosis after immobility HSDN C0242936 Center pain C0162679 Leukemic infiltration HSDN C0015970 Fever unknown origin C1963211 Pericarditis adverse event HSDN C1963091 Diarrhea adverse event C0018021 Goiter HSDN C0011991 Loose stools C0017689 Glucagonoma OrphaNet|UMLS|MalaCards C0027498 Nausea vomiting C0011880 Diabetic ketoacidosis UMLS C0042025 Urinary incontinence stress C0009240 Cognition HSDN C4085210 Usual severity pain C0751878 Vasculitis, central nervous system HSDN C3641756 Have diarrhea C0032965 Pregnancy complications, infectious HSDN C0426579 Anorexia symptom C0011570 Mental depression HSDN C0007859 Pain neck C0038016 Spondylolisthesis HSDN C2024893 Cardiovascular surgery result: fatigue C0152171 Idiopathic pulmonary hypertension OrphaNet C0011206 Delirium acute C0038358 Gastric ulcer HSDN C2984058 Have pain C0037315 Sleep apnea syndromes HSDN C0015468 Face pain C1253936 Synovial effusion HSDN C1279888 Proteinuria of undiagnosed cause C0013990 Pathological accumulation of air in tissues HSDN C0026821 Cramp C0004096 Asthma HSDN C0344428 Ventricular tachycardia by ecg finding C3151463 Cpvt3 MalaCards|HPO C0013595 Eczematous dermatitis C1839163 Thrombocytopenia 1 (disorder) HPO C2029884 Hearing loss by exam C0007222 Cardiovascular diseases HSDN C0013404 Respiratory difficulty C1336233 Stage iiib squamous cell carcinoma of lung UMLS C0424755 Fever symptoms C0014553 Absence epilepsy HSDN C1557397 Adverse event associated with pain C0237104 Spirituality HSDN C2936821 Spinal cerebrospinal fluid leak C0919691 Anastomotic leaks HSDN C0026838 Spasticity muscle C1837218 Cleft palate, isolated HSDN C4084767 Bothered by vomiting C0019066 Nontraumatic hemoperitoneum HSDN C4084767 Bothered by vomiting C1690964 Cataract HSDN C2029884 Hearing loss by exam C0007453 Cattle disease HSDN C0013604 Edematous C0013592 Ectropion HSDN C0030975 Disorders perception C0027659 Neoplasms, experimental HSDN C2984057 Have nausea C0004352 Autistic disorder HSDN C0003862 Pain joint C0001206 Acromegaly OrphaNet|HPO|MalaCards C0237326 Defecation pain C1839332 Rett syndrome, preserved speech variant HPO C1565249 Limitation, mobility C0677614 Encounter due to convalescence HSDN C4084769 Vomiting frequency C0011570 Mental depression HSDN C2141922 Pain in left hip C0810055 Other non-traumatic joint disorders UMLS C4084773 Bothered by weight gain C1963088 Cystitis adverse event HSDN C1145670 Failure respiratory C3809272 Lethal congenital contracture syndrome 5 MalaCards C0036572 Convulsion C0027627 Neoplasm metastasis HSDN C2315100 Pediatric failure to thrive C1864689 Microphthalmia, syndromic 6 (disorder) MalaCards|HPO C0426579 Anorexia symptom C1963067 Atrial fibrillation adverse event HSDN C0751265 Learning disability C3714980 Bardet-biedl syndrome 17 MalaCards C3641756 Have diarrhea C0026266 Mitral valve insufficiency HSDN C3641756 Have diarrhea C0034088 Pulmonary valve insufficiency HSDN C0240735 Personality change C1847650 Spongiform encephalopathy with neuropsychiatric features HPO|UMLS C1557397 Adverse event associated with pain C0032984 Pregnancy, abdominal HSDN C0039070 Collapse fleeting C0282607 Vascular neoplasms HSDN C4084767 Bothered by vomiting C1262481 Eosinophilic gastroenteritis OrphaNet|MalaCards C0033377 Caudal displacement C1527404 Female pseudo-turner syndrome HPO C1069915 Vertigo C3539923 Cdisc adas-cog - orientation summary score HSDN C0035229 Respiratory function impaired C2750414 Cap myopathy, tpm3-related HPO C3463815 Feel fatigue C0007785 Cerebral infarction HSDN C1963064 Anxiety adverse event C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C0013362 Dysarthrias C1260409 Myasthenia gravis without acute exacerbation MalaCards C0587246 Extremity weakness C3714933 Myopathy due to myoadenylate deaminase deficiency MalaCards C0231341 Aging premature C0006433 Burnout, professional HSDN C1963281 Vomiting adverse event C0025061 Disease of mediastinum HSDN C0522224 Palsied C0702221 Tactual discrimination HSDN C4084775 Usual severity weight loss C0017152 Gastritis HSDN C1963184 Nystagmus adverse event C3714932 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 MalaCards C2875628 Eyelid retraction left lower eyelid C0497217 Other disease of eye UMLS C0242936 Center pain C0393735 Headache disorders HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0038379 Eye deviation HSDN C0018784 Deafness sensorineural C0878544 Cardiomyopathies HSDN C0851578 Disorder sleep C0020701 Somatization disorder HSDN C3641756 Have diarrhea C0206171 Community acquired infections HSDN C1963184 Nystagmus adverse event C3280062 Leber congenital amaurosis 16 MalaCards C0241165 Skin thickening C1847836 Oculocutaneous albinism, type iv OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0001126 Renal tubular acidosis HSDN C0700078 Deep tendon reflex decrease C1832334 Charcot-marie-tooth disease, type 4d MalaCards|HPO C0007398 Catatonic C0700327 Clinical findings relating to memory HSDN C2024893 Cardiovascular surgery result: fatigue C0948264 Neuroborreliosis MalaCards C0002962 Angina C0031046 Pericarditis HSDN C2203646 Jaundice C0023467 Leukemia, myelocytic, acute HSDN C0349588 Stature short C2675897 1q21.1 contiguous gene deletion OrphaNet|MalaCards C2029884 Hearing loss by exam C0796121 Primrose syndrome MalaCards C0023012 Delay language C1968924 Autism, susceptibility to, 1 HPO C0036572 Convulsion C0152164 Cyclical vomiting syndrome (disorder) MalaCards C0424755 Fever symptoms C2827407 Infectious otitis media HSDN C0013428 Painful urination C0006736 Body stone HSDN C0162834 Hyperpigmentation C2677099 Crouzon syndrome with acanthosis nigricans (disorder) MalaCards C4084802 Usual severity diarrhea C1863236 Scid due to ada deficiency, early-onset HPO C0008031 Pain chest C0013808 Electroconvulsive therapy HSDN C0518090 Frequency of pain question C0005745 Blepharoptosis HSDN C1549543 Administration method - pain C0008309 Bile duct adenoma HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2711591 Infection by anisakidae MalaCards C0349489 Fetal hypoxia C0700327 Clinical findings relating to memory HSDN C2984058 Have pain C0020651 Hypotension, orthostatic HSDN C4085661 Usual severity nausea C1837218 Cleft palate, isolated HSDN C0233514 Behavior abnormal C0344488 Absence; cerebellum OrphaNet C0151786 Weakness muscle C1546847 Entity name part type - family HSDN C2024878 Cardiovascular surgery result: dyspnea C0023903 Liver neoplasms MalaCards|HSDN C0000737 Abdomen pain C0034088 Pulmonary valve insufficiency HSDN C0234146 Absent reflex C0795950 Corpus callosum agenesis neuronopathy MalaCards|HPO C0020673 Hypothermia (central) (local) C0014335 Enteritis HSDN C4085211 Pain distress question C0019357 Keratitis, herpetic HSDN C0030554 Abnormal sensation C1970820 Fabry disease, cardiac variant HPO C4085317 Diarrhea frequency C0011389 Dental plaque HSDN C0009676 Confusion state C0015230 Exanthema HSDN C0035229 Respiratory function impaired C3554235 Joubert syndrome 20 MalaCards C0700590 Diaphoresis excessive C1861848 Paragangliomas 4 MalaCards|HPO C0038002 Spleen enlargement C2752042 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi HPO C4085661 Usual severity nausea C4050613 Anxiety scale (basc-2) HSDN C0917816 Deficiency mental C1859773 Microphthalmia, syndromic 3 MalaCards|HPO C2237041 Shox gene with short stature C1510479 Neuralgic amyotrophy MalaCards|HPO C4084724 Usual severity constipation C0017658 Glomerulonephritis HSDN C4084727 Cough frequency C0025521 Inborn errors of metabolism HSDN C1963137 Hydrocephalus adverse event C0751291 Desmoplastic medulloblastoma MalaCards C0027796 Neuralgias C0039504 Injuries tendon HSDN C0018991 Paralysis one side of body C0751194 Hematoma, spinal subdural HSDN C1549543 Administration method - pain C0010403 Cryoglobulinemia HSDN C0042798 Vision dim C1850994 Foveal hypoplasia with anterior segment anomalies HPO C0231218 Malaise generalized C3899982 Bclc stage 0 hepatocellular carcinoma UMLS C1963281 Vomiting adverse event C0268579 Propionic acidemia HPO C0019079 Bloody sputum C0034074 Infarct pulmonary HSDN C0018772 Deafness C0795623 Hepatitis a vaccine, inactivated HSDN C1963252 Tremor adverse event C0020676 Hypothyroidism HSDN C0036572 Convulsion C3661860 Rasmussen syndrome, intractable UMLS C2919142 Short stature adverse event C0796055 Mercaptolactate-cysteine disulfiduria OrphaNet|MalaCards C0013421 Dystonia C1850406 Navajo neurohepatopathy MalaCards|HPO C0019825 Voice hoarseness C0010266 Cranial nerve diseases HSDN C4084769 Vomiting frequency C0024692 Mandible fracture HSDN C0151827 Pain eye C0751878 Vasculitis, central nervous system HSDN C1963086 Confusion adverse event C0001418 Adenocarcinoma HSDN C4084774 Have weight loss C1090821 Sepsis (invertebrate) HSDN C0009421 Comatose C1706377 Memory device component HSDN C0018772 Deafness C0031485 Phenylketonurias HSDN C1557397 Adverse event associated with pain C0029454 Osteopetrosis HSDN C0427055 Face weakness C0742090 Cerebral parietal cva UMLS C0004134 Dyssynergia C0025281 Meniere disease HSDN C0033774 Skin pruritus C0032460 Polycystic ovary syndrome HSDN C0010200 Cough symptom C0496775 Malignant neoplasm of abdominal part of esophagus MalaCards C0020615 Hypoglycemia nos C1864912 2-methylbutyryl-coa dehydrogenase deficiency HPO C4084776 Weight loss C1832386 Diabetes mellitus, transient neonatal, 1 OrphaNet|HPO|MalaCards C1384666 Decreased hearing C3150127 Bardet biedl syndrome 15 HPO C0013604 Edematous C0154743 Neuropathy ulnar HSDN C0349588 Stature short C3489787 Pituitary hormone deficiency, combined, 3 MalaCards C0851578 Disorder sleep C0022104 Irritable bowel syndrome HSDN C4085210 Usual severity pain C0019061 Hemolytic-uremic syndrome HSDN C3815497 Cough C0028433 Nose neoplasms HSDN C0917816 Deficiency mental C1836373 Muscular dystrophy, limb-girdle, type 2k MalaCards|HPO C0151786 Weakness muscle C0027686 Pathologic neovascularization HSDN C3887784 Decreased urine output C0022661 Kidney failure, chronic HSDN C4084767 Bothered by vomiting C0018817 Atrial septal defects HSDN C4084769 Vomiting frequency C0021390 Inflammatory bowel diseases HSDN C2984058 Have pain C0242966 Systemic inflammatory response syndrome HSDN C0085128 Cardiac output elevated C0039841 Thiamine deficiency HSDN C0518090 Frequency of pain question C0022423 Judgement HSDN C1963252 Tremor adverse event C0014544 Epilepsy HSDN C0030200 Intractable pain C0024141 Lupus erythematosus, systemic HSDN C0242936 Center pain C0033839 Pseudorabies HSDN C0151686 Growth retardation C0406729 Berlin syndrome MalaCards C1963063 Anorexia adverse event C0023240 Legionellosis MalaCards C0349588 Stature short C1858032 Cortical defects, wormian bones, and dentinogenesis imperfecta OrphaNet|MalaCards C3539890 Pelvic pain causes awakening at night C2984291 Glioblastoma multiforme pathway HSDN C1279888 Proteinuria of undiagnosed cause C0031117 Peripheral neuropathy HSDN C0085593 Chill C0376618 Endotoxemia HSDN C2315100 Pediatric failure to thrive C0340951 Erythrogenesis imperfecta MalaCards C4085211 Pain distress question C0560694 Bottles per feed HSDN C4085211 Pain distress question C3536741 Discordant ventriculoarterial connection HSDN C0019214 Hepatosplenomegaly C1704429 Hypoalphalipoproteinemia, familial MalaCards C3541349 Syncope C0338586 Vertebral artery dissection HSDN C0518090 Frequency of pain question C0376618 Endotoxemia HSDN C0009421 Comatose C0011854 Diabetes mellitus, insulin-dependent HSDN C0152459 Striae C0001231 Acth syndrome, ectopic MalaCards C0036572 Convulsion C0015300 Exophthalmos HSDN C0560024 Eyelid swelling C2751321 Macrocephaly, alopecia, cutis laxa, and scoliosis UMLS C0018777 Deafness, conductive C0265261 Multiple pterygium syndrome HPO C0009763 Conjunctiva inflammation C1274789 Ligneous conjunctivitis OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0085082 Fungemia HSDN C0518090 Frequency of pain question C0017154 Gastritis, atrophic HSDN C0518090 Frequency of pain question C0333355 Inflammatory disease of mucous membrane HSDN C0023015 Language handicap C0011581 Depressive disorder HSDN C0013362 Dysarthrias C0030569 Secondary parkinson disease HSDN C0751837 Gait ataxic C0037930 Spinal cord neoplasms HSDN C0042571 Vertigo subjective C1962983 Cataract adverse event HSDN C0020538 Hbp C0043119 Werner syndrome MalaCards|HPO C0013428 Painful urination C1511204 Bladder urachal adenocarcinoma UMLS C0424755 Fever symptoms C0398623 Thrombophilia HSDN C1963091 Diarrhea adverse event C0037933 Spinal diseases HSDN C0026838 Spasticity muscle C0302892 Congenital porencephaly OrphaNet|MalaCards C0043094 Weight gain C0017638 Glioma HSDN C0026838 Spasticity muscle C0751813 Chronic brain injury HSDN C2911645 Weight loss adverse event C0022821 Kyphosis deformity of spine HSDN C0151786 Weakness muscle C0518450 Spinal fractures HSDN C3539895 Pelvic pain occurs with bowel movement C0242350 Erectile dysfunction HSDN C0042571 Vertigo subjective C0026266 Mitral valve insufficiency HSDN C1963093 Dizziness adverse event C0015802 Femur fracture HSDN C0042024 Urine incontinence C0026850 Muscular dystrophy HSDN C0018772 Deafness C2930953 Halal setton wang syndrome MalaCards C1549543 Administration method - pain C2186740 Reported urticaria HSDN C0085631 Abnormal excitement C0010346 Crohn disease HSDN C0151889 Reflexes tendon increased C1833691 Otofaciocervical syndrome OrphaNet|HPO C2024893 Cardiovascular surgery result: fatigue C0038454 Cerebrovascular accident HSDN C1963091 Diarrhea adverse event C1384665 Hfe gene HSDN C4084773 Bothered by weight gain C0015397 Disorder of eye HSDN C0221752 Rbc urine C3150878 Hyperoxaluria, primary, type iii MalaCards C4085210 Usual severity pain C3245466 Observationvalue - trust HSDN C0150055 Pain chronic C0005695 Bladder neoplasm HSDN C4084802 Usual severity diarrhea C0023281 Leishmaniasis HSDN C0019079 Bloody sputum C0862651 Epidermoid carcinoma in situ of hypopharynx UMLS C1069915 Vertigo C0040053 Thrombosis HSDN C0522224 Palsied C0006277 Bronchitis HSDN C2984058 Have pain C0198632 Pneumoperitoneum HSDN C0948992 Lower extremity paresthesia C1839780 Fragile x tremor/ataxia syndrome MalaCards|UMLS C0028738 Nystagmus C0265339 Borjeson-forssman-lehmann syndrome MalaCards|HPO C1963281 Vomiting adverse event C2028283 History of premature birth HSDN C2024893 Cardiovascular surgery result: fatigue C0043352 Xerostomia HSDN C0032227 Effusion pleural C0004943 Behcet syndrome MalaCards|HPO C4084767 Bothered by vomiting C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C2024893 Cardiovascular surgery result: fatigue C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C0019214 Hepatosplenomegaly C0175703 Thrombocytopenia-absent radius syndrome MalaCards|HPO C0241137 Skin pallor C0035334 Retinitis pigmentosa HSDN C0242936 Center pain C0016978 Gallbladder neoplasm HSDN C4085548 Usual severity dizziness C0030920 Peptic ulcer HSDN C0917816 Deficiency mental C0268238 Triglyceride storage disease with ichthyosis MalaCards|HPO C1963071 Back pain adverse event C0016057 Fibrosarcoma HSDN C0271185 Metamorphopsia C0033847 Pseudoxanthoma elasticum MalaCards|HPO C1963093 Dizziness adverse event C0031941 Pineal gland neoplasm HSDN C1963281 Vomiting adverse event C0340629 Aortic aneurysm without mention of rupture nos HSDN C1959630 Eye pain adverse event C0242383 Age related macular degeneration HSDN C1963180 Neck pain adverse event C0018802 Congestive heart failure HSDN C0037763 Spasm C0521518 Muscle spasms of head and neck UMLS C0043094 Weight gain C0009651 Conditioning operant HSDN C4084774 Have weight loss C0039494 Temporomandibular joint disorders HSDN C2984058 Have pain C0038017 Congenital spondylolisthesis HSDN C0040485 Wryneck C0019284 Diaphragmatic hernia HSDN C3829611 Nausea frequency C3889576 Euphoria HSDN C2919142 Short stature adverse event C0334123 Histiocytosis, lipoid MalaCards C1963249 Tinnitus adverse event C0007873 Uterine cervical neoplasm HSDN C0026821 Cramp C1864649 Myasthenia, limb-girdle, with tubular aggregates HPO C0026838 Spasticity muscle C1846172 Hydranencephaly and abnormal genitalia HPO C0019521 Hiccoughs C0198632 Pneumoperitoneum HSDN C0013604 Edematous C0032987 Ectopic pregnancy HSDN C4084727 Cough frequency C0010668 Cystic adenomatoid malformation of lung, congenital HSDN C0009460 Communication impairment C0004941 Behavioral symptoms HSDN C0522224 Palsied C0010054 Coronary arteriosclerosis HSDN C4084725 Usual severity cough C0025289 Meningitis HSDN C0917816 Deficiency mental C0220989 Acquired partial lipodystrophy OrphaNet|HPO|MalaCards C0034155 Thrombotic thrombocytopenic purpura C0002890 Leukoerythroblastic anemia HSDN C0007758 Cerebellar ataxia C0021171 Bloch sulzberger syndrome HSDN C4084726 Distress cough C0034885 Rectal neoplasms HSDN C0454644 Delayed language development C2750082 Deafness, autosomal recessive 79 MalaCards|HPO C4084767 Bothered by vomiting C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C3887873 Hearing loss C0027438 Nasopharynx HSDN C0015672 Decreased energy C0041316 Lymph node tuberculosis DiseaseOntology|MalaCards C3641756 Have diarrhea C0023895 Liver diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0034494 Rabies (disorder) HSDN C0032617 High urine output C2242703 Cardio-renal syndrome HSDN C0151908 Dry skin C2698658 Orofaciodigital syndrome type 1 MalaCards C4049602 Hyperactivity C3280355 Chromosome 15q25 deletion syndrome MalaCards C4084766 Vomiting C1135841 Zoster sine eruptione HSDN C1384666 Decreased hearing C1847554 Ciliary dyskinesia, primary, 2 (disorder) MalaCards|HPO C0009676 Confusion state C1865322 Migraine, familial hemiplegic, 2 MalaCards|HPO C0000737 Abdomen pain C1623041 Breast-fed HSDN C0027497 Queasy C1861848 Paragangliomas 4 MalaCards C0030486 Extremity paralysis, lower C2984289 Melanoma pathway HSDN C2984058 Have pain C0020497 Cortical congenital hyperostosis HSDN C3887873 Hearing loss C0016470 Food allergy HSDN C2984057 Have nausea C0016045 Fibroma HSDN C1963091 Diarrhea adverse event C0238386 Cronkhite-canada disease MalaCards C0030232 Color loss C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C0028738 Nystagmus C2677434 Orofacial cleft 11 MalaCards C1962972 Proteinuria adverse event C0268742 Membranoproliferative glomerulonephritis, type i MalaCards C0015672 Decreased energy C0005974 Bone resorption HSDN C0030975 Disorders perception C0428953 Ecg infarction myocardial HSDN C0018784 Deafness sensorineural C1552262 Nurse practitioner - family HSDN C0004134 Dyssynergia C1968551 Mental retardation, x-linked 79 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0037928 Spinal cord diseases HSDN C0033774 Skin pruritus C0026769 Multiple sclerosis HSDN C0018681 Headache, cephalalgia C1705811 Terminology role entity HSDN C1963170 Hypothermia adverse event C0007762 Cerebellar neoplasms HSDN C2984058 Have pain C0003855 Arteriovenous fistula HSDN C0427202 Atony, muscular C0005416 Biliary dyskinesia UMLS C4085661 Usual severity nausea C1847843 Episodic ataxia, type 4 MalaCards C0018772 Deafness C1275081 Cardio-facio-cutaneous syndrome HPO C0018808 Murmur C3827868 Tachycardia by ecg finding HSDN C3463815 Feel fatigue C1963137 Hydrocephalus adverse event HSDN C0018834 Brash C1859049 Cchs with hirschsprung disease OrphaNet|HPO|MalaCards C0014591 Bleeding nose C0272309 Simple bruising MalaCards C4085862 Bothered by nausea C0011849 Diabetes mellitus HSDN C0016382 Cutaneous vascular engorgement C0796070 Microphthalmia, syndromic 7 MalaCards C0003862 Pain joint C0011875 Diabetic angiopathies HSDN C1962972 Proteinuria adverse event C0853697 Neutrophil count decreased HSDN C0011991 Loose stools C3658208 Disbioses HSDN C2024893 Cardiovascular surgery result: fatigue C0007099 Carcinoma in situ HSDN C0026821 Cramp C0038160 Staphylococcal infections HSDN C4084775 Usual severity weight loss C0023467 Leukemia, myelocytic, acute HSDN C0518090 Frequency of pain question C0035455 Rhinitis HSDN C0851578 Disorder sleep C0027412 Opioid-related disorders HSDN C0339251 Blood pigmentation of cornea C0162281 Corneal deposit UMLS C3887638 Failure to thrive in infant C0019880 Homocystinuria HSDN C0033774 Skin pruritus C2936739 Hyper-immunoglobulin e syndrome, autosomal dominant OrphaNet|HPO C0030552 Paralysis partial C0004096 Asthma HSDN C3146279 Coma C1269683 Major depressive disorder HSDN C2024893 Cardiovascular surgery result: fatigue C0003872 Arthritis, psoriatic HSDN C3887638 Failure to thrive in infant C0017923 Glycogen storage disease type iv MalaCards|HSDN|HPO C0015672 Decreased energy C0023470 Myeloid leukemia HSDN C2984058 Have pain C0014145 Yolk sac tumor HSDN C0019214 Hepatosplenomegaly C1849321 Sandhoff disease, juvenile type HPO C0751840 Pure alexia C0006112 Brain diseases, metabolic HSDN C0030552 Paralysis partial C1859317 Cataract and cardiomyopathy MalaCards|HPO C0557874 Global developmental delay C1859726 Arterial tortuosity syndrome MalaCards C0019079 Bloody sputum C0018789 Cardiac aneurysm HSDN C4084775 Usual severity weight loss C0015328 Behavior, exploratory HSDN C4084769 Vomiting frequency C1999266 Depression adverse event HSDN C0742292 Chest pain char typical C0403447 Chronic kidney insufficiency UMLS C0917816 Deficiency mental C3808977 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 MalaCards C0013604 Edematous C1962962 Hyperpigmentation adverse event HSDN C4084726 Distress cough C0018818 Ventricular septal defects HSDN C4084769 Vomiting frequency C2746068 Congenital idiopathic intestinal pseudoobstruction HPO C0860603 Anxiety symptom C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C1279888 Proteinuria of undiagnosed cause C0008370 Cholestasis HSDN C1963184 Nystagmus adverse event C0268226 Type i mucolipidosis OrphaNet|HPO C4084802 Usual severity diarrhea C0023473 Myeloid leukemia, chronic HSDN C0005745 Blepharoptosis C4014538 Helsmoortel-van der aa syndrome MalaCards C0241137 Skin pallor C0270858 Abdominal migraines MalaCards C0518090 Frequency of pain question C0221074 Depression, postpartum HSDN C0018772 Deafness C0009241 Cognition disorders HSDN C0034933 Abnormal reflexes C0007097 Carcinomas HSDN C3829611 Nausea frequency C0029456 Osteoporosis HSDN C2984058 Have pain C0265706 Gastroschisis HSDN C0015230 Exanthem C0857099 Extensive rash of forearm UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0011405 Pulp disorder HSDN C0007758 Cerebellar ataxia C0014544 Epilepsy HSDN C4085210 Usual severity pain C0001614 Adrenal cortex diseases HSDN C1963087 Constipation adverse event C0241158 Cicatrix skin HSDN C0042963 Symptoms vomiting C0026636 Mouth diseases HSDN C0036572 Convulsion C0001622 Adrenal gland hyperfunction HSDN C0522224 Palsied C0238357 Hyperkalemic periodic paralysis OrphaNet|MalaCards C0746674 Muscle weakness generalized C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards|HPO|UMLS C0015970 Fever unknown origin C0038160 Staphylococcal infections HSDN C0857305 Thrombocytopenia purpura C0023903 Liver neoplasms HSDN C4084784 Diarrhea C1829813 Malonic acidemia MalaCards C4085222 Nausea C1553188 Hemolysis - observation HSDN C4084769 Vomiting frequency C0162666 Mitochondrial encephalomyopathies HSDN C1549543 Administration method - pain C0149520 Acute cholecystitis HSDN C0018681 Headache, cephalalgia C1334963 Nevoid basal cell carcinoma syndrome associated medulloblastoma UMLS C1557397 Adverse event associated with pain C0020522 Delayed hypersensitivity HSDN C4084897 Sleep disturbance subordinate domain C1836437 B-cell immunodeficiency, distal limb anomalies, and urogenital malformations MalaCards C0015469 Facial paralysis C0015397 Disorder of eye HSDN C0013604 Edematous C0004364 Autoimmune diseases HSDN C0022346 Yellow skin C0033348 Language program HSDN C0494475 Seizure generalized tonic clonic C1836173 Generalized epilepsy and paroxysmal dyskinesia HPO C2202100 Pain in right hip C0810350 Non-traumatic joint disorders UMLS C0744002 Finger contraction C0744028 Finger spasm UMLS C0042514 Ventricular tachycardia C2930902 Bidirectional tachycardia MalaCards C2237041 Shox gene with short stature C2717836 Steroid sulfatase deficiency disease MalaCards C0019209 Large liver C0271693 Acquired generalized lipodystrophy MalaCards C4084726 Distress cough C0023473 Myeloid leukemia, chronic HSDN C1557397 Adverse event associated with pain C0243010 Viral encephalitis HSDN C1963281 Vomiting adverse event C0206062 Lung diseases, interstitial HSDN C1549543 Administration method - pain C0022353 Neonatal jaundice HSDN C1090821 Sepsis C2677349 Epidermolysis bullosa simplex with pyloric atresia OrphaNet|HPO|MalaCards C4085317 Diarrhea frequency C2073625 X-ray of chest: pleural effusion HSDN C0241137 Skin pallor C0235146 Emotionally high HSDN C0004604 Pain back C0272129 Donath-landsteiner hemolytic anemia OrphaNet|MalaCards C0010200 Cough symptom C0206613 Paramyxoviridae infections HSDN C3146279 Coma C1962971 Myocarditis adverse event HSDN C0040034 Thrombocytopenia C3469527 Fanconi anemia complementation group g MalaCards C4084774 Have weight loss C0268271 Gangliosidosis, generalized gm1, type 1 (disorder) OrphaNet|MalaCards C3244654 Sore throat brand of benzocaine & menthol C0023092 Lassa fever MalaCards C4085317 Diarrhea frequency C2748662 Mitchell-riley syndrome MalaCards C4085210 Usual severity pain C0006705 Calcium metabolism disorders HSDN C0242936 Center pain C0027667 Cancer origin unknown HSDN C0270948 Neurogenic muscular atrophy C3554605 Mc3dn2 MalaCards C3665386 Abnormal vision C2751780 Retinitis pigmentosa, juvenile, spata7-related HPO C0239134 Cough productive C0022660 Kidney failure, acute UMLS C0011570 Monopolar depression C0001206 Acromegaly OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0002880 Autoimmune hemolytic anemia HSDN C0850758 Pain pelvic C0042029 Urinary tract infection HSDN C4084773 Bothered by weight gain C1963064 Anxiety adverse event HSDN C0020578 Hyperventilate C3163620 Hypotension adverse event HSDN C0242936 Center pain C0029877 Ear inflammation HSDN C2984058 Have pain C0018839 Heat exhaustion HSDN C0011991 Loose stools C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0577698 Angina exertional C0004153 Atherosclerosis UMLS C0038002 Spleen enlargement C2937225 Biotin deficiency disease MalaCards C2024893 Cardiovascular surgery result: fatigue C0264743 Rheumatic fever without heart involvement MalaCards C0851578 Disorder sleep C0014848 Esophageal achalasia HSDN C4085210 Usual severity pain C0033046 Premenstrual syndrome HSDN C4084726 Distress cough C0004576 Babesiosis OrphaNet|MalaCards C0036572 Convulsion C0268611 Arakawa syndrome 2 MalaCards C2984058 Have pain C0015404 Eye infections, bacterial HSDN C1963071 Back pain adverse event C0037397 Behavior social HSDN C0042571 Vertigo subjective C0026269 Mitral valve stenosis HSDN C0242936 Center pain C0003490 Aortic arch syndrome HSDN C1557397 Adverse event associated with pain C0005604 Trauma birth HSDN C0497406 Over weight C0007786 Brain ischemia HSDN C0086565 Liver function abnormal C3281084 Congenital disorder of glycosylation, type ir MalaCards C3539020 Pelvic pain decreasing in frequency C0010695 Cystocele HSDN C2242996 Tingling C0238154 Epidural hematoma HSDN C0413252 Hypothermia due to exposure C0036984 Shock, surgical HSDN C0085636 Light sensitivity C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO|UMLS C4085210 Usual severity pain C0022672 Acute kidney tubular necrosis HSDN C2911645 Weight loss adverse event C0009241 Cognition disorders HSDN C4085549 Dizziness C1134719 Invasive ductal breast carcinoma HSDN C4084769 Vomiting frequency C2586211 Thrombosis of blood vessel HSDN C3829611 Nausea frequency C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0150055 Pain chronic C0024636 Malocclusion HSDN C4085661 Usual severity nausea C0018794 Heart block HSDN C2911645 Weight loss adverse event C0025063 Mediastinal neoplasms HSDN C0349506 Sun sensitivity C0024141 Lupus erythematosus, systemic MalaCards C4084769 Vomiting frequency C0021053 Immune system diseases HSDN C4084768 Usual severity vomiting C0268680 Biotin deficiency MalaCards C4085210 Usual severity pain C0019624 Histiocytosis, non-langerhans-cell HSDN C0349588 Stature short C0796080 Buenos aires type mental retardation OrphaNet|MalaCards C0023012 Delay language C0796225 Mental retardation, x-linked 19 HPO C0020672 Body temperature decreased C0006114 Cerebral edema HSDN C4084769 Vomiting frequency C0270858 Abdominal migraines MalaCards C4085210 Usual severity pain C0030215 Palate tumor HSDN C1549543 Administration method - pain C0040553 Toxocariasis HSDN C0221263 Cafe au lait spot C0027831 Neurofibromatosis 1 HPO C0031911 Pigment deposition C0008525 Choroideremia MalaCards C3641756 Have diarrhea C0017128 Fistula gastric HSDN C2024878 Cardiovascular surgery result: dyspnea C0242488 Acute lung injury HSDN C0036572 Convulsion C2931130 Clark-baraitser syndrome MalaCards|UMLS C1963281 Vomiting adverse event C0040559 Toxoplasmosis in animals HSDN C0015468 Face pain C3714514 Infection HSDN C0027497 Queasy C1265748 Torsion HSDN C0028738 Nystagmus C0265425 9p partial monosomy syndrome OrphaNet|MalaCards C1963252 Tremor adverse event C0032087 Plant poisoning HSDN C0005745 Blepharoptosis C1864436 Muenke syndrome OrphaNet|HPO|MalaCards C0018808 Murmur C0011581 Depressive disorder HSDN C4084774 Have weight loss C0036980 Shock, cardiogenic HSDN C0080233 Dental loss C1510460 Orofaciodigital syndrome i MalaCards C0043094 Weight gain C0027707 Nephritis, interstitial HSDN C1279888 Proteinuria of undiagnosed cause C1690964 Cataract HSDN C4084769 Vomiting frequency C0796561 Melanoma vaccines HSDN C0013132 Drooling C0162635 Angelman syndrome MalaCards|HPO C2984057 Have nausea C2004491 Cicatrix HSDN C0206160 Retic count elevated C0272051 Xerocytosis HPO C0151311 Cranial nerve palsy C0338078 Non-functioning pituitary gland neoplasm MalaCards C0027497 Queasy C3541306 Plasmodium measurement HSDN C1963184 Nystagmus adverse event C0796045 Ataxia-deafness-retardation syndrome MalaCards C3541349 Syncope C1832680 Cardiomyopathy, dilated, 1e MalaCards|HPO C2048469 Inability to impregnate after previous successful impregnation C0403800 Secondary male infertility UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C1836485 Charcot-marie-tooth disease, axonal, type 2a2 (disorder) HPO C0240715 Perineal lump C0154010 Benign neoplasm of epididymis UMLS C0522224 Palsied C0010246 Coxsackievirus infections HSDN C0015672 Decreased energy C2711227 Steatohepatitis HSDN C2919142 Short stature adverse event C2931685 Cantalamessa baldini ambrosi syndrome OrphaNet|MalaCards C4085210 Usual severity pain C0036130 Salpingitis HSDN C4084767 Bothered by vomiting C0393735 Headache disorders HSDN C0020672 Body temperature decreased C0011311 Dengue fever HSDN C0349588 Stature short C0795914 Crome syndrome OrphaNet|MalaCards C0011991 Loose stools C1963274 Vasculitis adverse event HSDN C0015970 Fever unknown origin C1535939 Pneumocystis jiroveci pneumonia HSDN C0362036 Coma and stupor nos C0009421 Comatose UMLS C0037763 Spasm C3714514 Infection HSDN C0026821 Cramp C0752287 Sleep disorders, intrinsic HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013712 Ego HSDN C1549543 Administration method - pain C0024537 Malaria, vivax HSDN C1963137 Hydrocephalus adverse event C0917890 Pineocytoma OrphaNet|MalaCards C0039070 Collapse fleeting C0017152 Gastritis HSDN C0151825 Ostalgia C0029396 Heterotopic ossification MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C2919115 Encounter due to bereavement HSDN C1962972 Proteinuria adverse event C0043241 Wound infection HSDN C3898969 Have been vomiting C0080178 Spina bifida HSDN C0042963 Symptoms vomiting C0997768 Glaucoma HSDN C0033774 Skin pruritus C0546826 Dermatophytosis body DiseaseOntology|MalaCards C0000737 Abdomen pain C0376300 Dengue shock syndrome OrphaNet|MalaCards C0221166 Paraparesis C0206635 Myelolipoma HSDN C0015300 Ocular proptosis C0220743 Childhood hypophosphatasia (disorder) MalaCards|HPO C4084769 Vomiting frequency C0027873 Neuromyelitis optica HSDN C0011124 Libido decreased C1858664 Hemochromatosis, type 3 MalaCards C0030554 Abnormal sensation C0033975 Psychotic disorders HSDN C0085636 Light sensitivity C0853637 Photophobia aggravated UMLS C2984058 Have pain C0009730 Spinal meningocele HSDN C0232466 Feeding difficulty C3554385 Congenital disorder of glycosylation, type iu MalaCards C0026821 Cramp C0012811 Colon diverticulum anatomic structure HSDN C0000737 Abdomen pain C0040100 Thymoma HSDN C0234146 Absent reflex C1844936 Spinocerebellar ataxia, x-linked 3 MalaCards C0010520 Skin cyanosis C2749559 Methemoglobinemia, type i HPO C0018681 Headache, cephalalgia C1864997 Majeed syndrome OrphaNet|HPO|MalaCards C0019825 Voice hoarseness C1510502 Oxyphilic adenoma HSDN C4084774 Have weight loss C0343398 Cyclosporiases HSDN C2700617 Irritation - emotion C3501891 Mitochondrial dna depletion myopathy, autosomal recessive MalaCards C0026838 Spasticity muscle C0001721 Emotional affect HSDN C2237041 Shox gene with short stature C1857511 Craniofacial dyssynostosis OrphaNet|MalaCards C0013196 Drug induced abnormal pigmentation of skin C0459805 Drug-induced melasma UMLS C3641756 Have diarrhea C0030354 Papilloma HSDN C0030193 Sense of pain C0005604 Trauma birth HSDN C2919142 Short stature adverse event C0268285 Adrenal hyperplasia, congenital, type 5 OrphaNet|HPO C0002622 Amnesias C0040053 Thrombosis HSDN C0003962 Ascites C0751674 Lymphangioleiomyomatosis MalaCards|HPO C0009806 Constipate C0003469 Anxiety disorders HSDN C1145670 Failure respiratory C0432198 Beemer langer syndrome MalaCards C4085222 Nausea C0024305 Lymphoma, non-hodgkin HSDN C3539890 Pelvic pain causes awakening at night C0006118 Brain neoplasms HSDN C0018926 Emesis bloody C0010068 Coronary heart disease HSDN C0424755 Fever symptoms C0039980 Chest injury HSDN C0005745 Blepharoptosis C0035934 Rubinstein-taybi syndrome MalaCards|HPO C4085549 Dizziness C0027627 Neoplasm metastasis HSDN C0030193 Sense of pain C0037997 Splenic diseases HSDN C0013404 Respiratory difficulty C0014836 Escherichia coli infections HSDN C0426579 Anorexia symptom C0153261 Histop. capsulatum infect. nos MalaCards C0020305 Fetal edema C1856302 Gsd iv, nonprogressive hepatic HPO C2032395 Pelvic pain on the left C0314657 Genetic predisposition HSDN C0039070 Collapse fleeting C0595812 Fistula route HSDN C0581299 Submental mass C0362076 Head problem UMLS C0085631 Abnormal excitement C0004238 Atrial fibrillation HSDN C4084767 Bothered by vomiting C0162869 Aneurysm, ruptured HSDN C0024032 Birth weight subnormal C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C0557874 Global developmental delay C3806634 Deafness, dystonia, and cerebral hypomyelination MalaCards C1963093 Dizziness adverse event C1999266 Depression adverse event HSDN C0030552 Paralysis partial C0015934 Fetal growth retardation HSDN C0026821 Cramp C0011570 Mental depression HSDN C1963170 Hypothermia adverse event C0020621 Hypokalemia HSDN C4084727 Cough frequency C1532560 Plasmacytoma - category HSDN C4084727 Cough frequency C0014118 Endocarditis HSDN C4085317 Diarrhea frequency C0242634 Diseases primates HSDN C3641756 Have diarrhea C0001139 Acinetobacter infection HSDN C0030232 Color loss C1548483 Leishmaniasis vaccine HSDN C0031154 Peritonitis, nos C0546323 Inferior vena cava membranous obstruction MalaCards C0221166 Paraparesis C0206744 T-lymphocytopenia, idiopathic cd4-positive HSDN C0557874 Global developmental delay C2675891 Chromosome 1q21.1 duplication syndrome OrphaNet|MalaCards C0004093 Asthenia C1384665 Hfe gene HSDN C0040485 Wryneck C0029443 Osteomyelitis HSDN C0036572 Convulsion C0030305 Pancreatitis HSDN C0003862 Pain joint C0015745 Ingestive behavior HSDN C3463815 Feel fatigue C1546949 Event consequence - death HSDN C2984058 Have pain C1510415 Osteosclerotic myeloma MalaCards C4084788 Have dizziness C0029888 Otitis media purulent HSDN C0332573 Macula C0034152 Henoch-schoenlein purpura MalaCards C0027497 Queasy C0812393 Cancer patients and suicide and depression HSDN C3178766 Nociceptive pain C0027765 Nervous system disorder HSDN C0024031 Back pain lower back C0314657 Genetic predisposition HSDN C4084802 Usual severity diarrhea C0029928 Ovarian diseases HSDN C4084776 Weight loss C1136321 Hiv-associated lipodystrophy syndrome HSDN C1963090 Dehydration adverse event C0341306 Microvillus inclusion disease HPO C2128090 Dip joint of left middle toe feels loose C1300268 Brachydactyly syndrome type c MalaCards C0344315 Mood depressed C1868681 Dystonia 12 HPO C0522224 Palsied C0032087 Plant poisoning HSDN C0518090 Frequency of pain question C0269185 Uterus retroverted HSDN C0004604 Pain back C0033871 Psychiatric status rating scales HSDN C3898969 Have been vomiting C0018794 Heart block HSDN C3887873 Hearing loss C0024841 Matrimony, matrimonial HSDN C0427055 Face weakness C1848947 Cold-induced sweating syndrome 1 HPO|UMLS C0917816 Deficiency mental C1852759 Papillorenal syndrome MalaCards|HPO C0812426 Kidney problem C0748197 Pyelonephritis lymphogranulomatous UMLS C0030193 Sense of pain C1145670 Respiratory failure HSDN C4084784 Diarrhea C1263846 Attention deficit hyperactivity disorder HSDN C0042024 Urine incontinence C0009663 Condylomata acuminata HSDN C0151205 Periorbital edema C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C4085549 Dizziness C0009240 Cognition HSDN C1963091 Diarrhea adverse event C1963215 Pneumothorax adverse event HSDN C0522224 Palsied C0015927 Intrauterine fetal demise HSDN C0085593 Chill C0025289 Meningitis UMLS C0413252 Hypothermia due to exposure C0036983 Septic shock HSDN C4084726 Distress cough C0040046 Thrombophlebitis HSDN C0010200 Cough symptom C0343206 Hypocomplementemic urticarial vasculitis MalaCards C4085210 Usual severity pain C0079027 Blood loss, surgical HSDN C0015672 Decreased energy C0948480 Coronary restenosis HSDN C0232461 Increased appetite C1843792 Frontotemporal lobar degeneration with tdp43 inclusions, grn-related HPO C1963091 Diarrhea adverse event C0376634 Craniofacial abnormalities HSDN C0424755 Fever symptoms C0031118 Peripheral nervous system neoplasms HSDN C2911647 Weight gain adverse event C0023892 Biliary cirrhosis HSDN C1557397 Adverse event associated with pain C0031046 Pericarditis HSDN C1000483 Genus anemia C2931518 Plexosarcoma MalaCards C0015469 Facial paralysis C1547940 Specimen source codes - ulcer HSDN C0460137 Push down or depress C0751208 Juvenile huntington disease MalaCards C2203646 Jaundice C0162869 Aneurysm, ruptured HSDN C1963063 Anorexia adverse event C1959620 Dihydropyrimidine dehydrogenase deficiency HSDN C0041657 Consciousness loss C0011581 Depressive disorder HSDN C4084784 Diarrhea C0039103 Synovitis HSDN C0033774 Skin pruritus C0268318 Cholestasis of pregnancy MalaCards|HPO C0004134 Dyssynergia C3281200 Leukoencephalopathy, brain calcifications, and cysts UMLS C0020538 Hbp C0033847 Pseudoxanthoma elasticum MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0024198 Lyme disease HSDN C0036659 Sensation disorder C0001418 Adenocarcinoma HSDN C0012569 Double vision C0206640 Ossifying fibroma HSDN C0024031 Back pain lower back C0023434 Chronic lymphocytic leukemia HSDN C0027497 Queasy C0026769 Multiple sclerosis HSDN C4084775 Usual severity weight loss C0596263 Carcinogenesis HSDN C0034151 Hyperglobulinemic purpura C0020473 Hyperlipidemia HSDN C4049644 Depression C1834570 Myoclonic dystonia HPO C3665492 Pigmentations C0345905 Intrahepatic cholangiocarcinoma MalaCards C2029884 Hearing loss by exam C0022865 Obstetric labor complications HSDN C4084774 Have weight loss C0017205 Gaucher disease HSDN C4085211 Pain distress question C0018818 Ventricular septal defects HSDN C0008031 Pain chest C0020540 Malignant hypertension UMLS C0026838 Spasticity muscle C0009375 Colonic neoplasms HSDN C2919142 Short stature adverse event C1866927 Smcr HPO C0042798 Vision dim C3805375 Albinism, oculocutaneous, type vi MalaCards C2315100 Pediatric failure to thrive C0010346 Crohn disease HSDN C2364111 Gustatory anesthesia C0027429 Nasal obstruction present finding HSDN C0013362 Dysarthrias C1834559 Continuous muscle fiber activity, hereditary OrphaNet|HPO C0010200 Cough symptom C1333420 Epithelial predominant pulmonary blastoma UMLS C0003079 Pupillary inequality C0006271 Bronchiolitis HSDN C0013456 Pain ear C0037199 Sinusitis UMLS C4085210 Usual severity pain C0043540 Zygomatic fracture HSDN C0030193 Sense of pain C0162835 Hypopigmentation disorder HSDN C0000727 Abdomen acute C0001621 Adrenal gland diseases HSDN C4085642 Level of joint stiffness C0265281 Metatropic dwarfism OrphaNet|HPO|MalaCards C4085549 Dizziness C0453996 Tobacco smoking HSDN C0019079 Bloody sputum C0014009 Empyema HSDN C2032395 Pelvic pain on the left C0037929 Spinal cord injuries HSDN C0015468 Face pain C0030581 Parotid neoplasms HSDN C0004604 Pain back C0007787 Transient ischemic attack HSDN C1963252 Tremor adverse event C1968551 Mental retardation, x-linked 79 MalaCards|HPO C2919142 Short stature adverse event C2932715 Pseudohypoparathyroidism type 1b OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0015467 Neuralgia facial HSDN C0042025 Urinary incontinence stress C0031154 Peritonitis HSDN C0042963 Symptoms vomiting C0039494 Temporomandibular joint disorders HSDN C4084802 Usual severity diarrhea C0079840 Milk allergy HSDN C0518090 Frequency of pain question C0004045 Asphyxia neonatorum HSDN C0015672 Decreased energy C1322286 Thymoma, type c MalaCards C0036572 Convulsion C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO|UMLS C0012833 Dizzy C0282507 Heat stress disorders HSDN C0010200 Cough symptom C0009917 Contracture HSDN C0012569 Double vision C0333157 Colloid cysts HSDN C1069915 Vertigo C0003850 Arteriosclerosis HSDN C3898969 Have been vomiting C0243026 Sepsis HSDN C0036572 Convulsion C0022078 Iris diseases HSDN C0557874 Global developmental delay C3698541 Ohdo syndrome, maat-kievit-brunner type MalaCards C3898969 Have been vomiting C3541306 Plasmodium measurement HSDN C4085549 Dizziness C0032344 Poisoning aspects HSDN C2203646 Jaundice C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0006370 Bulimia C1263846 Attention deficit hyperactivity disorder HSDN C4085661 Usual severity nausea C0041466 Typhoid fever HSDN C0006370 Bulimia C1288283 Atrophoderma maculatum HSDN C0003467 Angst C1568249 Usher syndrome, type ii MalaCards|HPO C0497406 Over weight C0018798 Congenital heart defects HSDN C1963184 Nystagmus adverse event C2931557 Chromosome 4 short arm deletion MalaCards C0010200 Cough symptom C0040558 Toxoplasmosis HSDN C1963184 Nystagmus adverse event C0206115 Wagr syndrome OrphaNet|HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0036239 Satiety HSDN C1963252 Tremor adverse event C1970180 Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation HPO C0030200 Intractable pain C0007621 Neoplastic cell transformation HSDN C1963180 Neck pain adverse event C0040136 Thyroid neoplasm HSDN C4082202 Sleep quality question C0206042 Fatal familial insomnia HPO C4084725 Usual severity cough C0024633 Gastroesophageal laceration-hemorrhage syndrome HSDN C0018772 Deafness C0265295 Jansen type metaphyseal chondrodysplasia HPO C0020580 Decreased sensation C0238154 Epidural hematoma HSDN C3274924 Have been coughing C0018939 Hematological disease HSDN C0020673 Hypothermia (central) (local) C0006110 Brain death HSDN C0019572 Hairiness C1868546 Patterson pseudoleprechaunism syndrome OrphaNet|MalaCards C0043094 Weight gain C0027726 Nephrotic syndrome HSDN C0036396 Sciatica C0013990 Pathological accumulation of air in tissues HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1504306 Anodontia genus HSDN C1963281 Vomiting adverse event C1290398 Cerebral arterial aneurysm HSDN C4085549 Dizziness C4048184 Trochlear nerve diseases HSDN C0026821 Cramp C0000889 Acanthosis nigricans HSDN C4084725 Usual severity cough C0026636 Mouth diseases HSDN C0018932 Bright red rectal bleeding C0079504 Hermanski-pudlak syndrome HPO C2984058 Have pain C0015403 Eye infections HSDN C0019079 Bloody sputum C2609414 Acute kidney injury HSDN C3815497 Cough C0015397 Disorder of eye HSDN C3274924 Have been coughing C0270611 Brain damage HSDN C0036572 Convulsion C3280154 Mental retardation, autosomal recessive 16 MalaCards C0011991 Loose stools C0401151 Chronic diarrhea UMLS C0497406 Over weight C0015671 Father HSDN C4084775 Usual severity weight loss C0023441 Leukemia, experimental HSDN C0011991 Loose stools C0013182 Drug allergy HSDN C0009676 Confusion state C0275148 Poisoning of animal by plant HSDN C4085211 Pain distress question C0038579 Substance abuse, intravenous HSDN C0042963 Symptoms vomiting C1522133 High cholesterol level HSDN C0851578 Disorder sleep C0020655 Hypothalamic diseases HSDN C0518090 Frequency of pain question C0006384 Bundle-branch block HSDN C4085549 Dizziness C0033893 Tension headache HSDN C0242936 Center pain C0334082 Nevus, epidermal (disorder) OrphaNet C2237041 Shox gene with short stature C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C4085210 Usual severity pain C0043253 Trauma blunt HSDN C4049644 Depression C1864112 Huntington disease-like 1 MalaCards|HPO C2984058 Have pain C0039131 Syphilis congenital HSDN C4085862 Bothered by nausea C0520946 Emotional hypersensitivity HSDN C4084723 Constipation C0305062 Tetanus toxoids HSDN C1963063 Anorexia adverse event C0010356 Cross infection HSDN C1963252 Tremor adverse event C0014072 Experimental autoimmune encephalomyelitis HSDN C4084766 Vomiting C0043528 Zoonoses HSDN C0013604 Edematous C0011633 Dermatomyositis OrphaNet|MalaCards C3539892 Pelvic pain in front C0021359 Infertility HSDN C0022346 Yellow skin C2981667 Stage iib distal bile duct cancer UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0008370 Cholestasis HSDN C3541349 Syncope C0037286 Skin neoplasms HSDN C0162834 Hyperpigmentation C1853354 Peeling skin syndrome, acral type MalaCards|HPO C4084727 Cough frequency C0023473 Myeloid leukemia, chronic HSDN C0851578 Disorder sleep C0035222 Respiratory distress syndrome, adult HSDN C0038002 Spleen enlargement C0039292 Tangier disease MalaCards|HPO C4042891 Sleep wake disorders C0079173 Craniomandibular disorders HSDN C4084774 Have weight loss C1962971 Myocarditis adverse event HSDN C0018784 Deafness sensorineural C0699744 Infection of ear HSDN C3539890 Pelvic pain causes awakening at night C0033873 Psychiatry HSDN C1519353 Skin eruption papular C0011644 Scleroderma OrphaNet|MalaCards C0020538 Hbp C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0009806 Constipate C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO|UMLS C0019572 Hairiness C0314657 Genetic predisposition HSDN C2024878 Cardiovascular surgery result: dyspnea C0016196 Chest flail HSDN C0221263 Cafe au lait spot C1850899 Gastrocutaneous syndrome MalaCards C0040822 D tremors C0019841 Classical swine fever HSDN C4084775 Usual severity weight loss C1861329 Spinal canal stenosis HSDN C0151908 Dry skin C1848413 Trichothiodystrophy, type 1 MalaCards C4084776 Weight loss C0024636 Malocclusion HSDN C0010520 Skin cyanosis C0029456 Osteoporosis HSDN C0033774 Skin pruritus C0035242 Respiratory tract diseases HSDN C0151786 Weakness muscle C0015230 Exanthema HSDN C0027497 Queasy C0019163 Hepatitis b DiseaseOntology|HSDN|MalaCards C0030193 Sense of pain C0027697 Nephritis HSDN C4084767 Bothered by vomiting C0019911 Hookworm infections HSDN C0011991 Loose stools C1456784 Paranoia HSDN C0039070 Collapse fleeting C0033923 Psychomotor function HSDN C2984057 Have nausea C0031046 Pericarditis HSDN C0024031 Back pain lower back C1290398 Cerebral arterial aneurysm HSDN C0151786 Weakness muscle C0009730 Spinal meningocele HSDN C0020538 Hbp C1567744 Alport syndrome, autosomal recessive MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C0027819 Neuroblastoma HSDN C0242936 Center pain C0022729 Klebsiella infections HSDN C1963066 Joint pain adverse event C1847593 Epiphyseal dysplasia, multiple, 4 MalaCards C4085661 Usual severity nausea C0014175 Endometriosis HSDN C0151889 Reflexes tendon increased C0796222 Mental retardation, x linked 16 MalaCards|HPO C0234979 Dysdiadochokinesia C1858501 Spinocerebellar ataxia 12 MalaCards|HPO|UMLS C0020673 Hypothermia (central) (local) C0013928 Fat embolism HSDN C0151889 Reflexes tendon increased C4015519 Epileptic encephalopathy, early infantile, 28 MalaCards C0022346 Yellow skin C3550398 Hyperbilirubinemia, shunt, primary UMLS C0234518 Speech slurred C0376329 New variant creutzfeldt-jakob disease MalaCards C0454644 Delayed language development C3150756 Chromosome 4q21 deletion syndrome MalaCards C0557874 Global developmental delay C2931816 Chromosome 2, monosomy 2q24 OrphaNet|MalaCards C0018772 Deafness C0020473 Hyperlipidemia HSDN C4085211 Pain distress question C0002878 Anemia, hemolytic HSDN C0026821 Cramp C0006705 Calcium metabolism disorders HSDN C0423707 Lateral femoral cutaneous neuralgia C0031121 Neuralgia peripheral UMLS C3898969 Have been vomiting C1963059 Adrenal insufficiency adverse event HSDN C0750937 Appendicular ataxia C3683483 Autosomal recessive cerebellar ataxia type 1 MalaCards C2911647 Weight gain adverse event C0042216 Poxvirus officinalis HSDN C0042755 Virilisation C0036341 Schizophrenia HSDN C3665492 Pigmentations C2713442 Polyposis, adenomatous intestinal MalaCards C4084766 Vomiting C0017181 Gastrointestinal hemorrhage HSDN C0413252 Hypothermia due to exposure C1864912 2-methylbutyryl-coa dehydrogenase deficiency HPO C0022346 Yellow skin C1708718 Localized non-resectable adult hepatocellular carcinoma UMLS C0018681 Headache, cephalalgia C0010043 Corneal ulcer HSDN C0033377 Caudal displacement C1855904 Acrofrontofacionasal dysostosis 2 MalaCards C0011991 Loose stools C0027932 Neurotic disorders HSDN C0043094 Weight gain C0039730 Thalassemia HSDN C0018681 Headache, cephalalgia C1266176 Atypical choroid plexus papilloma UMLS C1963252 Tremor adverse event C0038454 Cerebrovascular accident HSDN C1963281 Vomiting adverse event C0025290 Aseptic meningitis HSDN C0018524 Hallucinate C0004404 Autosuggestion HSDN C4085661 Usual severity nausea C0431109 Choroid plexus carcinoma HPO C0013404 Respiratory difficulty C0004933 Behavior modification technique HSDN C0151786 Weakness muscle C2986717 Anti-n-methyl-d-aspartate receptor encephalitis HSDN C0085631 Abnormal excitement C2984291 Glioblastoma multiforme pathway HSDN C0497247 Blood pressure elevation C0043119 Werner syndrome MalaCards|HPO C0035078 Failure kidney C0403443 Renal failure, progressive, with hypertension MalaCards C0013604 Edematous C0033575 Prostatic diseases HSDN C0557874 Global developmental delay C1857495 Cardiocranial syndrome MalaCards C3641756 Have diarrhea C1963148 Iron overload adverse event HSDN C2364111 Gustatory anesthesia C0023343 Leprosy HSDN C0020458 Hyperhydrosis C3810072 Palmoplantar keratoderma, nagashima type MalaCards C0036572 Convulsion C0032587 Polyradiculoneuropathy HSDN C4084776 Weight loss C0038325 Stevens-johnson syndrome OrphaNet|HSDN|HPO C0023012 Delay language C3151781 Ck syndrome MalaCards|HPO C0013604 Edematous C0021359 Infertility HSDN C1963091 Diarrhea adverse event C0025061 Disease of mediastinum HSDN C0007758 Cerebellar ataxia C0006023 Borna disease HSDN C0011175 Deficient fluid volume C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C3463815 Feel fatigue C0795623 Hepatitis a vaccine, inactivated HSDN C0009806 Constipate C0039231 Tachycardia HSDN C2024893 Cardiovascular surgery result: fatigue C0019294 Hernia, inguinal HSDN C0020903 Illusion C1457883 Aggressive reaction HSDN C0458090 Ureteric neuromuscular incoordination C0521619 Obstruction of pelviureteric junction UMLS C0557874 Global developmental delay C0265373 Fetal trimethadione syndrome OrphaNet|MalaCards C0018777 Deafness, conductive C0009241 Cognition disorders HSDN C4084724 Usual severity constipation C0221043 Liddle syndrome OrphaNet|HPO|MalaCards C0162298 Stiffness joints C0085261 Proteus syndrome HPO C3463815 Feel fatigue C0011848 Diabetes insipidus HSDN C1963249 Tinnitus adverse event C1136041 Familial acoustic neuroma OrphaNet|HPO C1549543 Administration method - pain C0037268 Skin abnormalities HSDN C3641756 Have diarrhea C0020179 Huntington disease HSDN C1963091 Diarrhea adverse event C0024282 Lymphocytosis HSDN C0242936 Center pain C0022650 Kidney calculi HSDN C0010520 Skin cyanosis C0036974 Shock HSDN C2242996 Tingling C0001197 Acrodermatitis HSDN C0040822 D tremors C0205788 Histiocytoid hemangioma HSDN C0311212 Migrating cheilosis C0021368 Inflammation UMLS C4085210 Usual severity pain C0033953 Psychosexual disorders HSDN C3539896 Pelvic pain occurs with urination C0015732 Fecal incontinence HSDN C0015468 Face pain C0022360 Jaw abnormalities HSDN C3829611 Nausea frequency C0038436 Post-traumatic stress disorder HSDN C0700590 Diaphoresis excessive C0870082 Hyperkeratosis MalaCards C0518090 Frequency of pain question C0003892 Neurogenic arthropathy HSDN C0013604 Edematous C0339289 Injury corneal HSDN C0013395 Indigestion C2711591 Infection by anisakidae HSDN C0010038 Corneal opacity disorder C2675650 Brain small vessel disease with axenfeld rieger anomaly HPO C0413252 Hypothermia due to exposure C0042487 Venous thrombosis HSDN C0015672 Decreased energy C0011854 Diabetes mellitus, insulin-dependent HSDN C4085211 Pain distress question C0162627 Skin diseases, bacterial HSDN C1557397 Adverse event associated with pain C0016507 Acquired foot deformities HSDN C0232466 Feeding difficulty C1853576 Diamond-blackfan anemia with microtia and cleft palate HPO C2132198 Abnormal blistering of the skin C0021100 Bullous impetigo OrphaNet|MalaCards C4085210 Usual severity pain C0026613 Motor skills disorders HSDN C1549543 Administration method - pain C0009447 Common variable immunodeficiency HSDN C0027497 Queasy C0241158 Cicatrix skin HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3273116 Gallbladder net MalaCards C0022568 Inflammation corneal C3665333 Keratitis-ichthyosis-deafness syndrome OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0018944 Hematoma HSDN C2188194 Unreasonable fears of specific object, activity, situation C0424184 Fear fly UMLS C0018681 Headache, cephalalgia C1833372 Hypocalciuric hypercalcemia, familial, type iii MalaCards C4085210 Usual severity pain C0035204 Respiration disorders HSDN C0022346 Yellow skin C0854797 Hepatoblastoma, resectable UMLS C0041657 Consciousness loss C1522136 Hypernatremia result HSDN C3641756 Have diarrhea C0016057 Fibrosarcoma HSDN C3665346 Loss sight C3280011 Brittle cornea syndrome 2 MalaCards C4084774 Have weight loss C0039103 Synovitis HSDN C3641755 Have constipation C0517555 Venous thrombosis after immobility HSDN C4084776 Weight loss C2362538 Thyroid stimulating hormone-producing pituitary tumor MalaCards C0015672 Decreased energy C0036323 Schistosomiasis HSDN C4084766 Vomiting C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C1000483 Genus anemia C2673913 Anemia, hypochromic microcytic, with iron overload HPO C0231835 Respiration rate increased C0206063 Radiation pneumonitis HSDN C0221166 Paraparesis C0014145 Yolk sac tumor HSDN C1557397 Adverse event associated with pain C2028283 History of premature birth HSDN C4084725 Usual severity cough C2930851 Intestinal lipophagic granulomatosis MalaCards C0000737 Abdomen pain C0042514 Tachycardia, ventricular HSDN C0424755 Fever symptoms C0015397 Disorder of eye HSDN C4084775 Usual severity weight loss C1720189 Episodic ataxia MalaCards C0015672 Decreased energy C0855101 Metastatic small lymphocytic lymphoma UMLS C0020639 Hypoproteinaemia C0268417 Pancreatic trypsinogen deficiency MalaCards C1963281 Vomiting adverse event C2004491 Cicatrix HSDN C2024893 Cardiovascular surgery result: fatigue C0027932 Neurotic disorders HSDN C0042024 Urine incontinence C3495554 Homocarnosinase deficiency MalaCards C4084725 Usual severity cough C0043251 Wounds and injuries HSDN C0015402 Hemorrhage eye C0035320 Retinal neovascularization HSDN C0008031 Pain chest C0035436 Rheumatic fever OrphaNet|MalaCards C0002962 Angina C0042769 Virus diseases HSDN C0151889 Reflexes tendon increased C4078861 Non ketotic hyperglycinemia syndrome MalaCards C0019209 Large liver C0026709 Mucopolysaccharidosis vi MalaCards|HPO C0030552 Paralysis partial C0206255 Malaria vaccine HSDN C3274924 Have been coughing C0023890 Liver cirrhosis HSDN C0242936 Center pain C0149721 Left ventricular hypertrophy HSDN C0242936 Center pain C0020640 Inherited factor ii deficiency HSDN C0018681 Headache, cephalalgia C3813553 Notch3 wt allele HSDN C1963170 Hypothermia adverse event C0005891 Bodies image HSDN C0242936 Center pain C0033054 Prenatal exposure delayed effects HSDN C0043094 Weight gain C0018916 Hemangioma HSDN C0332563 Papulae C2931072 Epidermolysa bullosa simplex and limb girdle muscular dystrophy MalaCards C0000737 Abdomen pain C0011880 Diabetic ketoacidosis HSDN|UMLS C0012833 Dizzy C0702221 Tactual discrimination HSDN C0043094 Weight gain C0022744 Knee injury HSDN C0522224 Palsied C0022602 Actinic keratosis HSDN C1963252 Tremor adverse event C0035801 Diseases rodent HSDN C1557397 Adverse event associated with pain C0035793 Rocky mountain spotted fever HSDN C0151786 Weakness muscle C0023470 Myeloid leukemia HSDN C0009806 Constipate C0035229 Respiratory insufficiency HSDN C0270948 Neurogenic muscular atrophy C0221406 Pituitary-dependent cushing's disease HPO C4084724 Usual severity constipation C0162283 Nephrogenic diabetes insipidus OrphaNet|HPO C0020673 Hypothermia (central) (local) C0043241 Wound infection HSDN C3641756 Have diarrhea C0008065 Childhood behavior HSDN C0004093 Asthenia C0376378 Barre lieou syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014145 Yolk sac tumor HSDN C0007758 Cerebellar ataxia C0752124 Spinocerebellar ataxia type 6 (disorder) MalaCards C0036396 Sciatica C0162870 Iliac artery aneurysm HSDN C0027497 Queasy C0011880 Diabetic ketoacidosis UMLS C0518090 Frequency of pain question C0037397 Behavior social HSDN C0018780 Frequencies hearing high loss C0854912 Pineal germinoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0014866 Esophageal stenosis HSDN C2024878 Cardiovascular surgery result: dyspnea C0025303 Meningococcal infections HSDN C1963180 Neck pain adverse event C0014461 Granuloma eosinophilic HSDN C0027066 Myoclonic jerking C1412759 Bckdha gene HSDN C0234512 Prosopagnosia C0037744 Perceptual spatial orientation HSDN C0041657 Consciousness loss C0037646 Psychiatric somatic therapy HSDN C0232695 Bowel sound decreased C0206734 Hemangioblastoma MalaCards C2984058 Have pain C0080274 Urinary retention HSDN C3829611 Nausea frequency C0439840 Reflex motion descriptor HSDN C0518090 Frequency of pain question C0030354 Papilloma HSDN C0040485 Wryneck C0751799 Brain hemorrhage, traumatic HSDN C0033774 Skin pruritus C0014805 Primary erythermalgia MalaCards|UMLS C0019209 Large liver C0272170 Shwachman syndrome HPO C0027497 Queasy C0003850 Arteriosclerosis HSDN C1557397 Adverse event associated with pain C1968835 Egot gene HSDN C0036572 Convulsion C0029182 Orbit (eye disorders) HSDN C3641755 Have constipation C1963216 Proctitis adverse event HSDN C1963086 Confusion adverse event C0013712 Ego HSDN C1963184 Nystagmus adverse event C0220701 Retinitis pigmentosa 1 MalaCards C0015672 Decreased energy C0007760 Cerebellar diseases HSDN C0917816 Deficiency mental C0473586 Michelin tire baby syndrome MalaCards|HPO C0000727 Abdomen acute C0041316 Lymph node tuberculosis HSDN C2024893 Cardiovascular surgery result: fatigue C0022716 Menkes kinky hair syndrome OrphaNet|HPO|MalaCards C0033774 Skin pruritus C1708350 Hereditary leiomyomatosis and renal cell cancer OrphaNet|HPO C4085548 Usual severity dizziness C0011551 Depersonalisation HSDN C4084726 Distress cough C0011981 Diaphragmatic eventration HSDN C4084788 Have dizziness C1836438 Familial neurocardiogenic syncope MalaCards C3665492 Pigmentations C1720965 Ectodermal dysplasia 3, anhidrotic MalaCards C0013604 Edematous C0398368 Lymphatic abnormalities HSDN C0851578 Disorder sleep C0040053 Thrombosis HSDN C0002170 Alopecia disorders C0265334 Pachyonychia congenita MalaCards|HPO C2315100 Pediatric failure to thrive C1421354 Umps gene HPO C0242936 Center pain C1138434 Disease, x-linked genetic HSDN C0010200 Cough symptom C0010380 Laryngotracheobronchitis, acute UMLS C1279888 Proteinuria of undiagnosed cause C0034040 Puerperal disorders HSDN C0577569 Mass of male genital structure C0333416 Granuloma sperm UMLS C0020672 Body temperature decreased C0036439 Scoliosis, unspecified HSDN C2911647 Weight gain adverse event C1090821 Sepsis (invertebrate) HSDN C0030193 Sense of pain C1711386 Keratinizing nasal cavity squamous cell carcinoma UMLS C3829611 Nausea frequency C0033860 Psoriasis HSDN C3539892 Pelvic pain in front C0007527 Cecal disease HSDN C1971624 Appetite absent C0025517 Metabolic diseases HSDN C0020455 Hypergammaglobulinemia C0024138 Lupus erythematosus, discoid HSDN C0013604 Edematous C0016085 Filariasis HSDN C0015938 Fetal macrosomia C0023895 Liver diseases HSDN C3539891 Pelvic pain to the rear C0269185 Uterus retroverted HSDN C0013604 Edematous C0344479 Spinal cord myelodysplasia HSDN C0042940 Disorder of voice C1623041 Breast-fed HSDN C0035232 Diaphragmatic paralysis C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0013604 Edematous C0041321 Tuberculosis, miliary HSDN C1963091 Diarrhea adverse event C0014038 Encephalitis HSDN C0026838 Spasticity muscle C0497327 Dementia MalaCards C0151889 Reflexes tendon increased C1850100 Parkinson disease 15, autosomal recessive (disorder) HPO C0018681 Headache, cephalalgia C0015029 Ethmoid sinusitis HSDN C4084784 Diarrhea C0032302 Mycoplasma pneumonia HSDN C0018681 Headache, cephalalgia C1537102 Inverted schneiderian papilloma UMLS C0003079 Pupillary inequality C2937358 Cerebral hemorrhage HSDN C2128732 Distal left leg soft tissue swelling C0037580 Soft tissue swelling UMLS C4084775 Usual severity weight loss C0717360 Disease lyme vaccine HSDN C1963063 Anorexia adverse event C0009404 Colorectal neoplasms HSDN C1963091 Diarrhea adverse event C0028738 Nystagmus HSDN C0026821 Cramp C0022658 Kidney diseases HSDN C0042024 Urine incontinence C0030767 Grouping peer HSDN C0019209 Large liver C1844376 Granulomatous disease, chronic, x-linked MalaCards|HPO C0030193 Sense of pain C0023290 Leishmaniasis, visceral HSDN C3641756 Have diarrhea C0085084 Motor neuron disease HSDN C0575081 Abnormal gait C1838281 Fryns macrocephaly OrphaNet|MalaCards C4085548 Usual severity dizziness C0020550 Hyperthyroidism HSDN C0019079 Bloody sputum C0010068 Coronary heart disease HSDN C4085641 Level of joint pain C0085293 Hepatitis e MalaCards C0522224 Palsied C0014670 Equinus contracture HSDN C0013604 Edematous C0037926 Compression of spinal cord HSDN C1549543 Administration method - pain C0040896 Trichinellosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0399352 Developmental absence of tooth HSDN C1963170 Hypothermia adverse event C1963164 Lymphopenia adverse event HSDN C0018681 Headache, cephalalgia C0152244 Bone cysts, aneurysmal HSDN C0007166 Cardiac output decreased C0032344 Poisoning aspects HSDN C4084769 Vomiting frequency C0034072 Cor pulmonale HSDN C0018524 Hallucinate C0038663 Suicide attempt HSDN C0231218 Malaise generalized C3273019 Early hepatocellular carcinoma UMLS C1963091 Diarrhea adverse event C0001721 Emotional affect HSDN C0917816 Deficiency mental C1845889 Mental retardation, x-linked 53 MalaCards C1549543 Administration method - pain C0036349 Paranoid schizophrenia HSDN C0015230 Exanthem C0086438 Hypogammaglobulinemia OrphaNet|MalaCards C4085548 Usual severity dizziness C0243026 Sepsis HSDN C0026838 Spasticity muscle C1855396 Alpha mannosidosis, type ii HPO C1069915 Vertigo C0033817 Pseudomonas infections HSDN C1963093 Dizziness adverse event C0037052 Sick sinus syndrome HSDN C3665346 Loss sight C1846170 Mental retardation, x-linked, syndromic 7 MalaCards C0015469 Facial paralysis C0021400 Influenza HSDN C0018784 Deafness sensorineural C1845068 Albinism-deafness syndrome OrphaNet|MalaCards C0557874 Global developmental delay C1291512 Beta-ureidopropionase deficiency MalaCards C1549543 Administration method - pain C0009946 Conversion disorder HSDN C0013428 Painful urination C1519925 Vaginal mucinous adenocarcinoma UMLS C0015799 Feminisation C0035358 Retroperitoneal neoplasm HSDN C0027497 Queasy C0025149 Medulloblastoma HSDN C0010038 Corneal opacity disorder C0342898 Apolipoprotein a-i deficiency OrphaNet|HPO C0037316 Not enough sleeping C0030920 Peptic ulcer HSDN C0038868 Supranuclear palsy progressive C0001418 Adenocarcinoma HSDN C0037771 Paraparesis spastic C3280977 Spastic ataxia 5, autosomal recessive UMLS C0036572 Convulsion C0026780 Mumps HSDN C4085661 Usual severity nausea C4019039 Intestinal obstruction co-occurrent and due to decreased peristalsis HSDN C4042891 Sleep wake disorders C0009475 Community mental health service HSDN C2919142 Short stature adverse event C1839311 Scott bryant graham syndrome OrphaNet|MalaCards C4084727 Cough frequency C0042138 Uterine neoplasms HSDN C0011991 Loose stools C1962976 Ventricular fibrillation adverse event HSDN C2984058 Have pain C0015652 Fascioliasis HSDN C0000737 Abdomen pain C2981400 Stage iic colorectal cancer UMLS C4085210 Usual severity pain C2350019 Solitary pulmonary nodule HSDN C0028961 Urine output decreased C0012739 Disseminated intravascular coagulation HSDN C0231528 Muscle pain generalized C0153261 Histop. capsulatum infect. nos MalaCards C0036572 Convulsion C0036986 Shock, traumatic HSDN C0030552 Paralysis partial C0024630 Malingering HSDN C0036659 Sensation disorder C0005491 Biofeedback HSDN C0850149 Cough dry C0085786 Hamman-rich syndrome MalaCards C3463815 Feel fatigue C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C2911647 Weight gain adverse event C0011609 Drug eruptions HSDN C4084776 Weight loss C0007138 Carcinoma, transitional cell HSDN C1963063 Anorexia adverse event C0009940 Convalescence HSDN C0030193 Sense of pain C0019195 Hepatitis, viral, human HSDN C0023015 Language handicap C0010068 Coronary heart disease HSDN C4084775 Usual severity weight loss C0153458 Pancreas head cancer malignant MalaCards C1963091 Diarrhea adverse event C1636667 Disorder characterized by eosinophilia HSDN C1557397 Adverse event associated with pain C0011311 Dengue fever HSDN C0010200 Cough symptom C0023092 Lassa fever OrphaNet|MalaCards C3641755 Have constipation C0020681 Sleep-related respiratory failure MalaCards C0018524 Hallucinate C0020649 Hypotension HSDN C0018524 Hallucinate C0700095 Central neuroblastoma HSDN C1384666 Decreased hearing C1319466 Barber say syndrome OrphaNet|HPO|MalaCards C0002962 Angina C0008370 Cholestasis HSDN C1971624 Appetite absent C0011226 Hepatitis d infection DiseaseOntology|MalaCards C0030794 Pelvis pain C0005586 Bipolar disorder HSDN C1527344 Dysphonia C1564560 Cartilage fracture HSDN C0019572 Hairiness C0151744 Myocardial ischemia HSDN C0009421 Comatose C1546654 Specimen source codes - granuloma HSDN C0000786 Abortion spontaneous C0043395 Yellow fever OrphaNet|MalaCards C0000737 Abdomen pain C0032227 Pleural effusion disorder UMLS C4084725 Usual severity cough C1175175 Severe acute respiratory syndrome HSDN C1557397 Adverse event associated with pain C0003614 Appendiceal neoplasms HSDN C0036572 Convulsion C0009326 Collagen diseases HSDN C2984058 Have pain C0023827 Liposarcoma HSDN C0000737 Abdomen pain C0041954 Ureteral diseases and syndromes HSDN C0575081 Abnormal gait C1848533 Ataxia with vitamin e deficiency OrphaNet|HPO C0012569 Double vision C1962983 Cataract adverse event HSDN C1962972 Proteinuria adverse event C0027412 Opioid-related disorders HSDN C3815497 Cough C0151744 Myocardial ischemia HSDN C3463815 Feel fatigue C0175816 Cold hemagglutinin disease OrphaNet|MalaCards C0017181 Gastrointestinal bleed C0016751 Hereditary fructose intolerance syndrome HPO C0009806 Constipate C0009450 Disease caused by microorganism HSDN C0851578 Disorder sleep C0001430 Adenoma HSDN C0020673 Hypothermia (central) (local) C4050613 Anxiety scale (basc-2) HSDN C0522224 Palsied C0014055 Encephalitis, epidemic HSDN C0030794 Pelvis pain C0029436 Bone disease, disappearing HSDN C0424755 Fever symptoms C0574960 Sacroiliitis HSDN C0850758 Pain pelvic C0037929 Spinal cord injuries HSDN C0522224 Palsied C0339143 Thyroid associated opthalmopathies HSDN C0013404 Respiratory difficulty C1762616 Meningioma, benign, no icd-o subtype HSDN C0030193 Sense of pain C0162316 Iron deficiency anemia HSDN C0013362 Dysarthrias C0398746 Gluthathione synthetase deficiency MalaCards|HPO C3541349 Syncope C0037397 Behavior social HSDN C1963274 Vasculitis adverse event C0014805 Primary erythermalgia MalaCards C3539020 Pelvic pain decreasing in frequency C0017412 Genital diseases, male HSDN C3641755 Have constipation C0038478 Struma ovarii HSDN C0002170 Alopecia disorders C1851970 Dyskeratosis congenita, autosomal dominant MalaCards|HPO C0518090 Frequency of pain question C0036130 Salpingitis HSDN C0518090 Frequency of pain question C0040761 Transposition of great vessels HSDN C1962957 Flushing adverse event C0031048 Pericarditis, constrictive HSDN C4084921 Usual severity itching C0546826 Dermatophytosis body DiseaseOntology|MalaCards C3641756 Have diarrhea C0035258 Restless legs syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0342443 Adrenal cushing's syndrome HSDN C0151798 Liver necrosis C0854176 Malignant hepato-biliary neoplasm MalaCards C1549543 Administration method - pain C0037299 Skin ulcer HSDN C1384666 Decreased hearing C1970482 Potocki-lupski syndrome MalaCards|HPO C0022346 Yellow skin C0032965 Pregnancy complications, infectious HSDN C0857305 Thrombocytopenia purpura C0005129 Bernard-soulier syndrome HSDN C2984058 Have pain C0028433 Nose neoplasms HSDN C4084776 Weight loss C0206042 Fatal familial insomnia HPO C0848203 Male pelvic pain C1881674 Medical device emits smoke HSDN C0036572 Convulsion C1631597 Ventricular tachycardia, catecholaminergic polymorphic, 1 (disorder) MalaCards|HPO|UMLS C2911647 Weight gain adverse event C0012979 Canine disease HSDN C3887873 Hearing loss C2984572 Malaria pathway HSDN C1384666 Decreased hearing C0027407 Narcotherapy HSDN C1279888 Proteinuria of undiagnosed cause C0037116 Silicosis HSDN C4085222 Nausea C1000587 Pemphigus HSDN C0028738 Nystagmus C0268384 Familial amyloid neuropathy, portuguese type MalaCards C2024878 Cardiovascular surgery result: dyspnea C0008350 Cholelithiasis HSDN C0000737 Abdomen pain C2981667 Stage iib distal bile duct cancer UMLS C0027066 Myoclonic jerking C0023521 Globoid cell leukodystrophy HSDN C4085211 Pain distress question C0015618 Families therapy HSDN C0020455 Hypergammaglobulinemia C0019693 Hiv infections HSDN C0020672 Body temperature decreased C0022744 Knee injury HSDN C1963087 Constipation adverse event C0012817 Diverticulum HSDN C0221232 Welts C0578871 Idiopathic micropapular urticaria UMLS C0242936 Center pain C0015456 Facial dermatoses HSDN C0424755 Fever symptoms C0015814 Femur head necrosis HSDN C0015672 Decreased energy C0005699 Blast phase UMLS C1963281 Vomiting adverse event C0153066 Murray valley encephalitis DiseaseOntology|MalaCards C0024031 Back pain lower back C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C3463815 Feel fatigue C0036439 Scoliosis, unspecified HSDN C3641756 Have diarrhea C0027726 Nephrotic syndrome HSDN C3641756 Have diarrhea C0001314 Acute disease HSDN C1549543 Administration method - pain C0018206 Granulosa cell tumor HSDN C3641756 Have diarrhea C1005359 Pica pica bird HSDN C2936821 Spinal cerebrospinal fluid leak C0520720 Cyst nerve root HSDN C0030193 Sense of pain C0006012 Borderline personality disorder HSDN C0043094 Weight gain C0013010 Cerebral lateralization HSDN C2984057 Have nausea C2937421 Prostatic hyperplasia HSDN C4085222 Nausea C0023530 Leukopenia HSDN C2984058 Have pain C0031154 Peritonitis HSDN C0042963 Symptoms vomiting C0026780 Mumps HSDN C0424755 Fever symptoms C0024110 Pulmonary abscess HSDN C1549543 Administration method - pain C0033367 Projective techniques HSDN C3829611 Nausea frequency C0025345 Menstruation disturbances HSDN C0042024 Urine incontinence C0021843 Intestinal obstruction HSDN C4084767 Bothered by vomiting C0036202 Sarcoidosis HSDN C1963071 Back pain adverse event C0008925 Cleft palate HSDN C2107732 Consistent heat intolerance C0343111 Naegeli syndrome MalaCards|HPO C4084802 Usual severity diarrhea C0027643 Neoplasm recurrence, local HSDN C0020578 Hyperventilate C0162557 Liver failure, acute HSDN C0917816 Deficiency mental C0011859 Lipoatrophic diabetes mellitus OrphaNet|HPO C1963091 Diarrhea adverse event C4014516 Diarrhea 7 MalaCards C0026838 Spasticity muscle C0034194 Pyloric stenosis HSDN C4084726 Distress cough C0178282 Hernia of abdominal cavity HSDN C0020673 Hypothermia (central) (local) C2936290 Femoracetabular impingement HSDN C1963281 Vomiting adverse event C0003864 Arthritis HSDN C0015230 Exanthem C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0017178 Gastrointestinal diseases HSDN C1963180 Neck pain adverse event C0376527 Neoplasm, skull base HSDN C1963093 Dizziness adverse event C0013364 Dysautonomia, familial HSDN C1549543 Administration method - pain C0002888 Anemia, megaloblastic HSDN C0030193 Sense of pain C0041954 Ureteral diseases and syndromes HSDN C0518090 Frequency of pain question C0007140 Carcinosarcoma HSDN C4085548 Usual severity dizziness C0036421 Systemic scleroderma HSDN C0023014 Developmental disorder language C0001973 Alcoholic intoxication, chronic HSDN C4084775 Usual severity weight loss C0017160 Gastroenteritis HSDN C0518090 Frequency of pain question C0033936 Psychoses, alcoholic HSDN C3539022 Pelvic pain decreasing in severity C0002871 Anemia HSDN C0036572 Convulsion C1855995 L-2-hydroxyglutaric aciduria OrphaNet|UMLS|HPO|MalaCards C4084768 Usual severity vomiting C0023473 Myeloid leukemia, chronic HSDN C0040822 D tremors C0022336 Creutzfeldt-jakob disease MalaCards C0018991 Paralysis one side of body C0007222 Cardiovascular diseases HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036982 Shock, hemorrhagic HSDN C0042963 Symptoms vomiting C3539615 Nci ctep sdc gestational trophoblastic disease sub-category terminology HSDN C1963137 Hydrocephalus adverse event C0206719 Central neurocytoma MalaCards C0017672 Pain tongue C0812393 Cancer patients and suicide and depression HSDN C0030193 Sense of pain C1959600 Obscure african cardiomyopathy HSDN C1963184 Nystagmus adverse event C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards|HPO C0750937 Appendicular ataxia C1843891 Spinocerebellar ataxia 21 HPO C4085549 Dizziness C0036357 Psychology, schizophrenic HSDN C0007758 Cerebellar ataxia C0220756 Niemann-pick disease, type c OrphaNet|HSDN|HPO|MalaCards C3815497 Cough C0022658 Kidney diseases HSDN C0577560 Eye mass C0521727 Pyogranulomatous conjunctivitis UMLS C2096293 Ent surgical result ear vertigo C0751291 Desmoplastic medulloblastoma MalaCards C4020887 Photodysphoria C0152085 Post-dysenteric reactive arthropathy nos MalaCards C0018524 Hallucinate C0010598 Cyclothymic disorder HSDN C0013604 Edematous C1864843 Combined oxidative phosphorylation deficiency 2 MalaCards|HPO C4084775 Usual severity weight loss C0028768 Obsessive-compulsive disorder HSDN C0039070 Collapse fleeting C0741011 Anemia symptomatic UMLS C3146279 Coma C0079731 B-cell lymphomas HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027962 Melanocytic nevus HSDN C0015970 Fever unknown origin C1261473 Sarcoma HSDN C0026821 Cramp C0006118 Brain neoplasms HSDN C0018989 Paresis of one side of body C0742450 Cns basal ganglia caudate cva UMLS C0008031 Pain chest C0017181 Gastrointestinal hemorrhage HSDN|UMLS C0031154 Peritonitis, nos C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C0031256 Petechia C0796126 Aicardi-goutieres syndrome 1 HPO C0010520 Skin cyanosis C0019284 Diaphragmatic hernia HSDN C4084766 Vomiting C0023418 Leukemia HSDN C0020578 Hyperventilate C0010068 Coronary heart disease HSDN C0007758 Cerebellar ataxia C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C1963071 Back pain adverse event C0017185 Gastrointestinal neoplasms HSDN C0004941 Behavioral symptoms C1866983 Scleroderma, familial progressive MalaCards C1384666 Decreased hearing C0022568 Keratitis HSDN C0234979 Dysdiadochokinesia C1866282 Ceroid lipofuscinosis, neuronal, 6 MalaCards C1557397 Adverse event associated with pain C0085648 Synovial cyst HSDN C3539896 Pelvic pain occurs with urination C0041960 Ureterocele HSDN C3887638 Failure to thrive in infant C0795841 Jacobsen distal 11q deletion syndrome MalaCards C2984058 Have pain C0149721 Left ventricular hypertrophy HSDN C2984058 Have pain C0042580 Vesico-ureteral reflux HSDN C1557397 Adverse event associated with pain C1546847 Entity name part type - family HSDN C0013911 Emaciate C0221018 Hereditary sideroblastic anemia HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0006434 Burn injury HSDN C0424755 Fever symptoms C0036690 Septicemia HSDN C0007398 Catatonic C0038522 Subacute sclerosing panencephalitis HSDN C0030193 Sense of pain C2748536 Leukocyte adhesion deficiency, type iii MalaCards|HPO C0030552 Paralysis partial C0003803 Arnold chiari malformation HSDN C0857305 Thrombocytopenia purpura C0002892 Anemia, pernicious HSDN C0013404 Respiratory difficulty C2827407 Infectious otitis media HSDN C0000737 Abdomen pain C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C0518090 Frequency of pain question C0033999 Pterygium HSDN C4085862 Bothered by nausea C0036421 Systemic scleroderma HSDN C0232466 Feeding difficulty C1853736 Congenital disorder of glycosylation, type iib MalaCards C0026826 High muscle tone C2752001 Growth retardation, developmental delay, coarse facies, and early death HPO C0040822 D tremors C0020179 Huntington disease HSDN C3146279 Coma C0024141 Lupus erythematosus, systemic HSDN C0019825 Voice hoarseness C0345985 Skin neoplasm keratoacanthoma eruptive MalaCards C0033377 Caudal displacement C2931196 Craniofacial dysostosis type 1 MalaCards C3641756 Have diarrhea C0038587 Substance withdrawal syndrome HSDN C2984058 Have pain C0030807 Pemphigus, nos HSDN C3641756 Have diarrhea C0719874 Diaper rash brand HSDN C0030193 Sense of pain C0005818 Blood platelet disorders HSDN C3539020 Pelvic pain decreasing in frequency C0015558 Fallopian tube neoplasms HSDN C0042963 Symptoms vomiting C0026603 Motion sickness UMLS C0007758 Cerebellar ataxia C1838951 Leigh syndrome due to mitochondrial complex i deficiency HPO C4085211 Pain distress question C0014122 Subacute bacterial endocarditis HSDN C0041667 Low weight C0795939 Aminopterin syndrome sine aminopterin MalaCards C3541349 Syncope C0022660 Kidney failure, acute HSDN C2024893 Cardiovascular surgery result: fatigue C0023267 Fibroid tumor HSDN C3146279 Coma C1423541 Vangl2 gene HSDN C2237041 Shox gene with short stature C2931622 Ring chromosome 7 OrphaNet|MalaCards C0022346 Yellow skin C1518869 Pancreatic intraductal papillary-mucinous neoplasm UMLS C0036572 Convulsion C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate MalaCards|HPO C0206160 Retic count elevated C0024534 Malaria, cerebral HSDN C1549543 Administration method - pain C0339143 Thyroid associated opthalmopathies HSDN C0033774 Skin pruritus C0235660 Galactorrhea not associated with childbirth HSDN C0018775 Hearing loss bilateral C0025286 Meningioma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027877 Neuronal ceroid-lipofuscinoses HSDN C0206160 Retic count elevated C0037054 Sickle cell trait MalaCards C0013456 Pain ear C0019364 Herpes zoster ophthalmicus HSDN C0151786 Weakness muscle C0024841 Matrimony, matrimonial HSDN C1579931 Depressed - symptom C1527406 Rhizomelic pseudopolyarthritis MalaCards C4084774 Have weight loss C0004114 Astrocytoma HSDN C0600142 Flash hot C0236969 Substance-related disorders HSDN C0010200 Cough symptom C0276932 Schistosoma; intercalatum DiseaseOntology C1963071 Back pain adverse event C1527429 Increased blood npn HSDN C4084769 Vomiting frequency C0020179 Huntington disease HSDN C1549543 Administration method - pain C0852795 Increased insulin level HSDN C3539023 Pelvic pain increasing in frequency C0009404 Colorectal neoplasms HSDN C3641755 Have constipation C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4085642 Level of joint stiffness C1860042 Antley-bixler syndrome with disordered steroidogenesis MalaCards C0751837 Gait ataxic C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO|UMLS C1971624 Appetite absent C0021400 Influenza HSDN C2203646 Jaundice C1963067 Atrial fibrillation adverse event HSDN C0240382 Mouth swelling C0858647 Oral mucosa swollen UMLS C3665347 Vision impaired C4014440 Mitochondrial complex iii deficiency, nuclear type 8 MalaCards C3178766 Nociceptive pain C0005967 Bone neoplasms HSDN C0012833 Dizzy C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C4084784 Diarrhea C1959626 Mevalonic aciduria MalaCards|HPO C1963281 Vomiting adverse event C0206172 Diabetic foot HSDN C4085210 Usual severity pain C0042024 Urinary incontinence HSDN C0497406 Over weight C0038941 Incisional infection HSDN C1997332 Lingual dysarthria C0013362 Dysarthria UMLS C0576456 Poor feeding C1864840 Combined oxidative phosphorylation deficiency 3 MalaCards C0033774 Skin pruritus C0040336 Tobacco use disorder HSDN C0455988 Hydrops fetalis non immune C1842704 Gaucher disease, perinatal lethal MalaCards|HPO C0015672 Decreased energy C0003794 Arm injury HSDN C0026821 Cramp C0041952 Uerterolithiasis HSDN C2984058 Have pain C0024301 Lymphoma, follicular HSDN C4084776 Weight loss C0009326 Collagen diseases HSDN C2024893 Cardiovascular surgery result: fatigue C0033785 Pseudarthrosis HSDN C4084769 Vomiting frequency C0887833 Carcinoma, pancreatic ductal HSDN C2984058 Have pain C0005398 Cholestasis, extrahepatic HSDN C3829611 Nausea frequency C0027659 Neoplasms, experimental HSDN C0518090 Frequency of pain question C0008350 Cholelithiasis HSDN C0011206 Delirium acute C0027932 Neurotic disorders HSDN C0020903 Illusion C0042797 Monocular vision HSDN C1963281 Vomiting adverse event C0008626 Congenital chromosomal disease HSDN C0162834 Hyperpigmentation C3809233 Noonan syndrome 8 MalaCards C2984058 Have pain C0376545 Hematologic neoplasms HSDN C0009806 Constipate C0020649 Hypotension HSDN C0030193 Sense of pain C0241158 Cicatrix skin HSDN C0012569 Double vision C0009765 Conjunctivitis, acute hemorrhagic HSDN C0002624 Amnesia retrograde C0162869 Aneurysm, ruptured HSDN C0013604 Edematous C1836876 Pierson syndrome MalaCards|HPO C4085548 Usual severity dizziness C0087012 Ataxia, spinocerebellar HSDN C3815497 Cough C0031090 Periodontal diseases HSDN C1963093 Dizziness adverse event C0035352 Disease, retrocochlear HSDN C0340288 Angina stable C0232347 No-reflow phenomenon HSDN C4084727 Cough frequency C0032453 Polychondritis, relapsing OrphaNet|MalaCards C4085222 Nausea C0022116 Ischemia HSDN C0019825 Voice hoarseness C0023895 Liver diseases HSDN C0013404 Respiratory difficulty C2711227 Steatohepatitis HSDN C3641755 Have constipation C0038358 Gastric ulcer HSDN C0009792 Consciousness disorder C0023788 Whipple disease HSDN C2237041 Shox gene with short stature C0406723 Growth retardation, alopecia, pseudoanodontia and optic atrophy OrphaNet|HPO|MalaCards C0349588 Stature short C1849382 Familial rhizomelic dysplasia OrphaNet|MalaCards C4085211 Pain distress question C0026636 Mouth diseases HSDN C4085642 Level of joint stiffness C1859316 Cataract-alopecia-sclerodactyly syndrome OrphaNet|MalaCards C4084774 Have weight loss C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0026838 Spasticity muscle C0029124 Optic atrophy MalaCards C0474512 Blood in faeces symptom C0019080 Hemorrhage UMLS C4085549 Dizziness C0409959 Osteoarthritis, knee HSDN C4084775 Usual severity weight loss C0007273 Carotid artery diseases HSDN C0038990 Sweats C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C3274924 Have been coughing C0038663 Suicide attempt HSDN C4084776 Weight loss C2936779 Hydroxymethylbilane synthase deficiency MalaCards C2024893 Cardiovascular surgery result: fatigue C0034067 Pulmonary emphysema HSDN C3539020 Pelvic pain decreasing in frequency C0005491 Biofeedback HSDN C3641756 Have diarrhea C1690964 Cataract HSDN C0015230 Exanthem C0521480 Phytophotodermatitis, nos UMLS C1963087 Constipation adverse event C0014544 Epilepsy HSDN C4084773 Bothered by weight gain C0016470 Food allergy HSDN C1549543 Administration method - pain C0272375 Antithrombin iii deficiency HSDN C2107732 Consistent heat intolerance C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia MalaCards C0042571 Vertigo subjective C0023055 Laryngeal neoplasm HSDN C1963252 Tremor adverse event C0036202 Sarcoidosis HSDN C0000731 Abdomen distention C0795956 Chylomicron retention disease OrphaNet|HPO|MalaCards C3641755 Have constipation C0014356 Enterocolitis HSDN C0018780 Frequencies hearing high loss C0041296 Tuberculosis HSDN C1384666 Decreased hearing C0034067 Pulmonary emphysema HSDN C0557874 Global developmental delay C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards C0042420 Vasovagal episode C1836438 Familial neurocardiogenic syncope MalaCards C1557397 Adverse event associated with pain C1135957 Narrative HSDN C0030552 Paralysis partial C0014061 Tick-borne encephalitis HSDN C2242996 Tingling C0015397 Disorder of eye HSDN C4084766 Vomiting C0009946 Conversion disorder HSDN C0264272 Nose discharge, purulent C1285329 Infection of head UMLS C4084776 Weight loss C0036221 Mast-cell sarcoma OrphaNet|MalaCards C0022346 Yellow skin C0027819 Neuroblastoma HSDN C4084784 Diarrhea C0035334 Retinitis pigmentosa HSDN C0009421 Comatose C0003864 Arthritis HSDN C4085210 Usual severity pain C0162836 Hidradenitis suppurativa HSDN C1549543 Administration method - pain C0037997 Splenic diseases HSDN C0002962 Angina C0033873 Psychiatry HSDN C2024878 Cardiovascular surgery result: dyspnea C0016658 Fracture bone HSDN C0007758 Cerebellar ataxia C1546847 Entity name part type - family HSDN C0013528 Echo speech C0035934 Rubinstein-taybi syndrome HSDN C0878773 Bladder hyperactive C0314657 Genetic predisposition HSDN C0242936 Center pain C0009442 Common bile duct neoplasms HSDN C0035078 Failure kidney C0340992 Cryoglobulinemic; vasculitis OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0700644 Primary extrapulmonary coccidioidomycosis MalaCards C1279888 Proteinuria of undiagnosed cause C3888013 Hypnoses HSDN C0041657 Consciousness loss C1829703 Carnitine palmitoyl transferase 1a deficiency OrphaNet|HPO C0010200 Cough symptom C0007097 Carcinomas HSDN C4084768 Usual severity vomiting C1636667 Disorder characterized by eosinophilia HSDN C0034933 Abnormal reflexes C0043251 Wounds and injuries HSDN C0013362 Dysarthrias C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy HPO C0042928 Paralysis vocal cord C0238461 Anaplastic thyroid carcinoma OrphaNet C4085211 Pain distress question C0018021 Goiter HSDN C4084784 Diarrhea C0018199 Granuloma, plasma cell HSDN C4085210 Usual severity pain C0034212 Pyoderma HSDN C3898969 Have been vomiting C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0270790 Quadriparesis C3662077 Paralytic syndrome of all four limbs UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0019123 Hemothorax HSDN C0040264 Ear ringing sound C0022665 Kidney neoplasm HSDN C0752303 Manifestation, urological C0520946 Emotional hypersensitivity HSDN C3463815 Feel fatigue C3489856 Cold hypersensitivity MalaCards C1963091 Diarrhea adverse event C3495559 Juvenile arthritis HSDN C0023380 Lethargy C0033680 Protein-losing enteropathies HSDN C0085593 Chill C0002986 Fabry disease HSDN C0234378 Postural tremor C0751779 Action myoclonus-renal failure syndrome HPO|UMLS C0022346 Yellow skin C0272052 Rh deficiency syndrome HPO C0015469 Facial paralysis C0035243 Respiratory tract infections HSDN C0042928 Paralysis vocal cord C0162871 Aortic aneurysm, abdominal HSDN C4084769 Vomiting frequency C0525045 Mood disorders HSDN C0011570 Monopolar depression C0751072 Frontotemporal lobar degeneration MalaCards C0427055 Face weakness C1850126 Osteopetrosis, mild autosomal recessive form MalaCards|HPO C0041105 Jaw spasm C0029171 Oral submucosal fibrosis, including of tongue MalaCards C4084784 Diarrhea C0009244 Behavioral cognitive therapy HSDN C1963170 Hypothermia adverse event C0009241 Cognition disorders HSDN C2984058 Have pain C0025958 Microcephaly HSDN C0018991 Paralysis one side of body C0027122 Myositis ossificans HSDN C4085548 Usual severity dizziness C0020456 Hyperglycemia HSDN C0013604 Edematous C0030286 Pancreatic diseases HSDN C4084802 Usual severity diarrhea C0009862 Contraception behavior HSDN C0042023 Urination frequency C1997249 Neuralgia, pudendal MalaCards C3887873 Hearing loss C0062527 Hepatitis b vaccine HSDN C3829611 Nausea frequency C0403447 Chronic kidney insufficiency HSDN C2203646 Jaundice C3469186 Hemochromatosis, type 1 HSDN C0557874 Global developmental delay C1859298 Spinocerebellar ataxia, autosomal recessive 2 MalaCards|HPO C4084766 Vomiting C0264766 Rheumatic mitral stenosis HSDN C3641756 Have diarrhea C0524910 Hepatitis c, chronic HSDN C2029884 Hearing loss by exam C0029408 Degenerative polyarthritis HSDN C0003469 Anxiety disorder C4014803 Acth-independent macronodular adrenal hyperplasia 2 MalaCards C0009398 Color vision defects C1458155 Mammary neoplasms HSDN C1962972 Proteinuria adverse event C0023220 Leg injury HSDN C0018524 Hallucinate C0036690 Septicemia HSDN C4085210 Usual severity pain C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0000737 Abdomen pain C0005426 Biliary tract neoplasm HSDN C0004310 Auditory disorder process C0007137 Squamous cell carcinoma HSDN C0751401 Ophthalmoparesis C0162671 Melas syndrome MalaCards|HPO C0040822 D tremors C0007097 Carcinomas HSDN C1963065 Apnea adverse event C0023448 Lymphoid leukemia HSDN C0242936 Center pain C1704275 Pyomyositis HSDN C0023015 Language handicap C1962986 Glaucoma adverse event HSDN C0009806 Constipate C0039144 Syringomyelia HSDN C1384666 Decreased hearing C0340427 Familial dilated cardiomyopathy MalaCards C0018524 Hallucinate C0022658 Kidney diseases HSDN C4085210 Usual severity pain C0002514 Amino acid metabolism, inborn errors HSDN C0041657 Consciousness loss C0024961 Injuries maxillofacial HSDN C0042963 Symptoms vomiting C1290613 Disease of upper gastrointestinal tract UMLS C0018991 Paralysis one side of body C2984289 Melanoma pathway HSDN C0013404 Respiratory difficulty C0041315 Tuberculosis, laryngeal HSDN C0086565 Liver function abnormal C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C0742288 Chest pain char non specific C0741025 Chest problem UMLS C0018681 Headache, cephalalgia C0035334 Retinitis pigmentosa HSDN C0030975 Disorders perception C0003838 Arterial occlusive diseases HSDN C0086565 Liver function abnormal C1414525 Fah gene HPO C4084775 Usual severity weight loss C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0231218 Malaise generalized C3272461 Ampulla of vater pancreatobiliary type adenocarcinoma UMLS C0751349 Eyelid myoclonus C0268608 Deficiency of dihydrofolate reductase MalaCards C1557397 Adverse event associated with pain C0007774 Cerebral arterial diseases HSDN C0034933 Abnormal reflexes C0152179 Disease vagus nerve HSDN C4084802 Usual severity diarrhea C1269683 Major depressive disorder HSDN C0040822 D tremors C1970180 Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation HPO|UMLS C2029884 Hearing loss by exam C0008476 Chondromatosis, synovial HSDN C0917816 Deficiency mental C1832814 Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant MalaCards C1069915 Vertigo C0014474 Ependymoma HSDN C1557397 Adverse event associated with pain C0950123 Inborn genetic disease HSDN C0027498 Nausea vomiting C0025149 Medulloblastoma MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0042830 Perception visual HSDN C4084774 Have weight loss C0432217 Wolcott-rallison syndrome OrphaNet|HPO C0002170 Alopecia disorders C1863204 Adult syndrome OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0162834 Hyperpigmentation HSDN C0015672 Decreased energy C1370868 Refractory cml UMLS C1963184 Nystagmus adverse event C3151470 Amyloidosis, leptomeningeal, transthyretin-related HPO C0018681 Headache, cephalalgia C0268193 Nadh cytochrome b5 reductase deficiency HPO|UMLS C3539890 Pelvic pain causes awakening at night C0206767 Neoplasms, cystic, mucinous, and serous HSDN C0751495 Seizure focal C1832814 Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant MalaCards C4084724 Usual severity constipation C0035243 Respiratory tract infections HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1961100 Erectile dysfunction adverse event HSDN C1549543 Administration method - pain C0008088 Child psychiatry HSDN C0410919 Foetal bradycardia C0455991 Fetal dysrhythmia UMLS C3203358 Alveolar hypoventilation C0018802 Congestive heart failure HSDN C0011175 Deficient fluid volume C0079683 Herlitz disease OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0018802 Congestive heart failure HSDN C1145670 Failure respiratory C2673266 Krabbe disease, atypical, due to saposin a deficiency HPO C3887638 Failure to thrive in infant C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C3146279 Coma C0152025 Polyneuropathy HSDN C4085661 Usual severity nausea C0032966 Complication, neoplastic pregnancy HSDN C4084724 Usual severity constipation C3179349 Gastrointestinal stromal sarcoma OrphaNet|HPO|MalaCards C0009421 Comatose C0008325 Cholecystitis HSDN C0020578 Hyperventilate C3810814 Myocardial infarction ecg assessment HSDN C0750426 Wbc elevated C0409818 Chronic infantile neurological, cutaneous, and articular syndrome OrphaNet|HPO|MalaCards C4084766 Vomiting C0000814 Abortion, missed HSDN C2127658 Snapping sensation in both shoulders C0581348 Snapping shoulder UMLS C1962972 Proteinuria adverse event C3808953 Nephrotic syndrome, type 8 MalaCards C1549543 Administration method - pain C0525045 Mood disorders HSDN C4084768 Usual severity vomiting C0018674 Head trauma HSDN C1963180 Neck pain adverse event C0010054 Coronary arteriosclerosis HSDN C0036572 Convulsion C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C0231712 Gait waddling C0432213 Irapa type spondyloepimetaphyseal dysplasia MalaCards|UMLS C0002965 Crescendo angina C0025202 Melanoma HSDN C1069915 Vertigo C0009241 Cognition disorders HSDN C0009024 Clonus C0878676 6-pyruvoyl-tetrahydropterin synthase deficiency MalaCards|HPO C0398650 Idiopathic thrombocytopenia purpura C0079772 T-cell lymphoma HSDN C0013404 Respiratory difficulty C0017658 Glomerulonephritis HSDN C0042571 Vertigo subjective C0001430 Adenoma HSDN C0042928 Paralysis vocal cord C0020517 Hypersensitivity HSDN C0033774 Skin pruritus C1610547 Production class code - pleasure HSDN C0011991 Loose stools C3887662 Intraspinal neoplasm HSDN C0013395 Indigestion C0032965 Pregnancy complications, infectious HSDN C0042024 Urine incontinence C0043246 Laceration HSDN C0019079 Bloody sputum C0854983 Lung adenocarcinoma, recurrent UMLS C0426579 Anorexia symptom C0036421 Systemic scleroderma HSDN C0028081 Night sweat C0854726 Stage i mixed cellularity hodgkin's disease below the diaphragm UMLS C0037771 Paraparesis spastic C0023772 Lipid metabolism, inborn errors HSDN C1963071 Back pain adverse event C1963090 Dehydration adverse event HSDN C0020505 Excessive eating C0011854 Diabetes mellitus, insulin-dependent MalaCards C0015468 Face pain C0005940 Bone diseases HSDN C4084725 Usual severity cough C0018024 Goiter, retrosternal HSDN C0151827 Pain eye C0028432 Nose diseases HSDN C0033774 Skin pruritus C0997768 Glaucoma HSDN C1090821 Sepsis C0221026 X-linked agammaglobulinemia OrphaNet|HPO C0042024 Urine incontinence C0023176 Lead poisoning HSDN C0013604 Edematous C0162818 Skin diseases, papulosquamous HSDN C0013132 Drooling C0019202 Hepatolenticular degeneration MalaCards|HPO C3641756 Have diarrhea C0018889 Helminthiasis HSDN C0042798 Vision dim C1970416 Xfe progeroid syndrome MalaCards|HPO C4084727 Cough frequency C0032851 Disease poultry HSDN C0018772 Deafness C0032963 Pregnancy complications, cardiovascular HSDN C4084776 Weight loss C0007282 Carotid stenosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0025205 Melanoma, experimental HSDN C0013604 Edematous C0031099 Periodontitis HSDN C2984058 Have pain C0008626 Congenital chromosomal disease HSDN C4084784 Diarrhea C0022353 Neonatal jaundice HSDN C1963071 Back pain adverse event C0152244 Bone cysts, aneurysmal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023493 Adult t-cell lymphoma/leukemia HSDN C0030554 Abnormal sensation C0027051 Myocardial infarction HSDN C0036572 Convulsion C0272295 Purpura, rheumatica MalaCards C0037763 Spasm C2984291 Glioblastoma multiforme pathway HSDN C0026826 High muscle tone C1863843 Neuronal intranuclear inclusion disease OrphaNet|MalaCards C0239574 Fever low grade C0006277 Bronchitis DiseaseOntology|MalaCards C0000727 Abdomen acute C0020295 Hydronephrosis HSDN C1384666 Decreased hearing C0001193 Apert syndrome MalaCards|HSDN|HPO C0004134 Dyssynergia C1136041 Familial acoustic neuroma OrphaNet|HPO C0013404 Respiratory difficulty C0040962 Tricuspid valve prolapse HSDN C0036572 Convulsion C0265425 9p partial monosomy syndrome OrphaNet|MalaCards C0004604 Pain back C0014852 Esophageal diseases HSDN C0011991 Loose stools C0342443 Adrenal cushing's syndrome HSDN C0033774 Skin pruritus C0018767 Auditory sense HSDN C4085211 Pain distress question C0004659 Bacteriuria HSDN C0019079 Bloody sputum C0014544 Epilepsy HSDN C0010201 Cough chronic C0234533 Generalized seizures UMLS C0030193 Sense of pain C0241910 Hepatitis, autoimmune HSDN C0010520 Skin cyanosis C0020492 Hyperostosis HSDN C0042963 Symptoms vomiting C0010481 Cushing syndrome HSDN C4049602 Hyperactivity C1843181 Noonan syndrome-like disorder with loose anagen hair HPO C0025287 Meningitis-like C0031069 Familial mediterranean fever HSDN C0041657 Consciousness loss C1142166 Brugada syndrome (disorder) HSDN C4085549 Dizziness C0033845 Pseudotumor cerebri HSDN C4084766 Vomiting C3541306 Plasmodium measurement HSDN C2024878 Cardiovascular surgery result: dyspnea C2981150 Uranostaphyloschisis HSDN C1963180 Neck pain adverse event C0036202 Sarcoidosis HSDN C1069915 Vertigo C0524910 Hepatitis c, chronic HSDN C0700078 Deep tendon reflex decrease C2678051 Mental retardation, x-linked 94 (disorder) MalaCards|HPO C0557874 Global developmental delay C3537048 Trisomy 18 MalaCards C0036572 Convulsion C2931736 Ehlers-danlos syndrome with progeroid facies and mild mental retardation OrphaNet|MalaCards C1963281 Vomiting adverse event C0948089 Acute coronary syndrome HSDN C0030794 Pelvis pain C0020517 Hypersensitivity HSDN C0518090 Frequency of pain question C0206488 Peer review, health care HSDN C0014591 Bleeding nose C4015537 Thrombocytopenia 5 MalaCards C0013421 Dystonia C0023795 Lipoid proteinosis of urbach and wiethe OrphaNet|HPO C0575081 Abnormal gait C0544012 Aberfeld's syndrome MalaCards C2984058 Have pain C0024720 Anxiety scale, manifest HSDN C0151740 Intracranial hypertension C0406723 Growth retardation, alopecia, pseudoanodontia and optic atrophy MalaCards|HPO C0000737 Abdomen pain C0268250 Gaucher disease, type 2 (disorder) MalaCards C0002962 Angina C0039685 Tetralogy of fallot HSDN C4084724 Usual severity constipation C0036864 Sexual relations HSDN C1384666 Decreased hearing C3888081 L-2-hydroxyglutaric acidemia MalaCards C0518090 Frequency of pain question C1306577 Dies patient HSDN C0033377 Caudal displacement C1302995 Congenital fibrosis of the extraocular muscles MalaCards C2984058 Have pain C0003184 Anthropology HSDN C0242670 Chronic vegetative state C0021400 Influenza HSDN C0040264 Ear ringing sound C0018798 Congenital heart defects HSDN C1557397 Adverse event associated with pain C0033906 Psychological theories HSDN C0020903 Illusion C2349049 Unit of infective dose HSDN C0151786 Weakness muscle C0234143 Neurological muscle weakness UMLS C0002965 Crescendo angina C0023370 Aortic occlusion distal chronic HSDN C0240715 Perineal lump C1302539 Vaginal condyloma UMLS C4084766 Vomiting C0020541 Hypertension, portal HSDN C0004604 Pain back C0027667 Cancer origin unknown HSDN C3463815 Feel fatigue C0334463 Malignant fibrous histiocytoma MalaCards C0410918 Baseline fetal tachycardia C0455991 Fetal dysrhythmia UMLS C0037763 Spasm C1412297 Aic gene HSDN C0003910 Articulation disorder C0017675 Glossitis HSDN C1963237 Insomnia adverse event C0751254 Creutzfeldt-jakob disease, familial MalaCards C1963281 Vomiting adverse event C0036216 Sarcoma, experimental HSDN C2315100 Pediatric failure to thrive C3809006 Cardiofaciocutaneous syndrome 3 MalaCards C0039239 Tachycardia sinus C0406645 Amyopathic dermatomyositis MalaCards C1069915 Vertigo C0062527 Hepatitis b vaccine HSDN C2237041 Shox gene with short stature C1845167 Dent disease 2 MalaCards|HPO C0036572 Convulsion C0220743 Childhood hypophosphatasia (disorder) MalaCards|HPO|UMLS C0232513 Premature tooth loss C1846142 Hoyeraal-hreidarsson syndrome MalaCards C0003962 Ascites C0585274 Periodic syndrome HPO C0600142 Flash hot C0007097 Carcinomas HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0009187 Coccidiosis HSDN C0004604 Pain back C0016124 Finger injury HSDN C0019079 Bloody sputum C0039685 Tetralogy of fallot HSDN C0151686 Growth retardation C1864498 Renal tubular acidosis, distal, autosomal recessive MalaCards|HPO C4085862 Bothered by nausea C0702221 Tactual discrimination HSDN C0349588 Stature short C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C0026826 High muscle tone C0152156 Dystocia HSDN C0040264 Ear ringing sound C1832425 Deafness, autosomal dominant 9 MalaCards|HPO C0518090 Frequency of pain question C0238461 Anaplastic thyroid carcinoma OrphaNet C3815497 Cough C0149931 Migraine disorders HSDN C1961131 Cough adverse event C0021843 Intestinal obstruction HSDN C0009806 Constipate C1333866 Grade 1 colon adenocarcinoma UMLS C4085211 Pain distress question C0042258 Vaginal neoplasms HSDN C0424755 Fever symptoms C0004364 Autoimmune diseases HSDN C0009421 Comatose C2930674 Babesioses, human MalaCards C0012569 Double vision C0004760 Air pressure-related disorder HSDN C0007758 Cerebellar ataxia C0007766 Intracranial aneurysm HSDN C2919142 Short stature adverse event C0796101 Digito-orofacial syndrome viii MalaCards C2242996 Tingling C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C4084727 Cough frequency C2931785 Juvenile dermatomyositis MalaCards C0027497 Queasy C0009374 Colonic disease, functional HSDN C0020796 Profoundly mentally retarded C2748910 Rett syndrome, atypical MalaCards|HPO C0264599 Aphonia paralytica C0264633 Voice disorder due to transsexualism UMLS C2911647 Weight gain adverse event C0400966 Non-alcoholic fatty liver disease HSDN C0231528 Muscle pain generalized C0008055 Chikungunya fever HSDN C1549543 Administration method - pain C1328252 Mucocutaneous leishmaniasis HSDN C0518090 Frequency of pain question C0079840 Milk allergy HSDN C0030193 Sense of pain C3463897 Hydatidiform mole, recurrent, 1 HSDN C1557397 Adverse event associated with pain C0085084 Motor neuron disease HSDN C0026821 Cramp C0878578 Orthostatic tremor primary OrphaNet|MalaCards C4084767 Bothered by vomiting C0024215 Lymphangiectasis, intestinal HSDN C0150055 Pain chronic C0238442 Symphysis pubis, separation HSDN C0042940 Disorder of voice C1548578 Location characteristic id - smoking HSDN C0012833 Dizzy C0042075 Urologic diseases HSDN C2203646 Jaundice C0039131 Syphilis congenital HSDN C0013604 Edematous C0015459 Face injury HSDN C0042928 Paralysis vocal cord C0036202 Sarcoidosis HSDN C1963091 Diarrhea adverse event C0035091 Renal tubular transport, inborn errors HSDN C4084724 Usual severity constipation C0242342 Sheehan syndrome MalaCards C0242670 Chronic vegetative state C0015671 Father HSDN C3887638 Failure to thrive in infant C0024121 Lung neoplasms HSDN C2700617 Irritation - emotion C0272199 Familial hemophagocytic lymphocytosis MalaCards C0018784 Deafness sensorineural C0153132 Juvenile neurosyphilis unspec. DiseaseOntology|MalaCards C4050613 Anxiety C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0392678 Impaired swallowing C0424605 Developmental delay (disorder) UMLS C4084784 Diarrhea C0007762 Cerebellar neoplasms HSDN C4084776 Weight loss C0027708 Nephroblastoma HSDN|HPO C0015468 Face pain C0270932 Neuropathy paraneoplastic HSDN C3641756 Have diarrhea C1548483 Leishmaniasis vaccine HSDN C0011206 Delirium acute C0001580 Adolescent behavior HSDN C2024878 Cardiovascular surgery result: dyspnea C0030354 Papilloma HSDN C0520909 Ponv C0014859 Esophageal neoplasms HSDN C4084766 Vomiting C0023267 Fibroid tumor HSDN C0349588 Stature short C1861448 Growth hormone deficiency with wormian bones, cardiac anomaly, and brachycamptodactyly OrphaNet|MalaCards C0042798 Vision dim C0029182 Orbit (eye disorders) HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0271865 Autoimmune hypoparathyroidism MalaCards C0036572 Convulsion C0018482 Haemophilus infections HSDN C0020450 Hyperemesis gravidarum C0221074 Depression, postpartum HSDN C0557874 Global developmental delay C3180937 15q11.2 microdeletion MalaCards C0030193 Sense of pain C1334183 Inflammatory pseudotumor, intracranial UMLS C0085593 Chill C4048826 Mud fever MalaCards C0344435 Ventricular fibrillation by ecg finding C2678485 Long qt syndrome 9 (disorder) MalaCards C2911645 Weight loss adverse event C1691228 Cystic kidney diseases HSDN C0020538 Hbp C0002066 Alkaptonuria MalaCards|HPO C0007398 Catatonic C0206085 Kleine-levin syndrome HSDN C0349506 Sun sensitivity C0162569 Hepatoerythropoietic porphyria OrphaNet|HPO|MalaCards C1963093 Dizziness adverse event C0043251 Wounds and injuries HSDN C0020580 Decreased sensation C0161410 Accessory nerve injuries HSDN C1549543 Administration method - pain C0019357 Keratitis, herpetic HSDN C0149793 Transient monocular blindness C0027743 Nerve compression syndrome HSDN C0002962 Angina C0020507 Hyperplasia HSDN C1963063 Anorexia adverse event C0040559 Toxoplasmosis in animals HSDN C2919142 Short stature adverse event C1739384 Angel shaped phalangoepiphyseal dysplasia OrphaNet|HPO|MalaCards C0042755 Virilisation C0037286 Skin neoplasms HSDN C0022346 Yellow skin C0432217 Wolcott-rallison syndrome HPO C0497247 Blood pressure elevation C1852406 Cutis gyrata syndrome of beare and stevenson MalaCards|HPO C4084767 Bothered by vomiting C0019069 Hemophilia a HSDN C1557397 Adverse event associated with pain C0037005 Shoulder dislocation HSDN C0022346 Yellow skin C1861455 Stomatocytosis i HPO|UMLS C1549543 Administration method - pain C0206488 Peer review, health care HSDN C0021359 Infertility C3551716 Cortisone reductase deficiency 1 MalaCards C1279888 Proteinuria of undiagnosed cause C0004775 Bartter disease HSDN C0242936 Center pain C0034628 Radius fracture HSDN C0424755 Fever symptoms C2674259 Cnmdu1 HPO C0151825 Ostalgia C0342642 Autosomal dominant hypophosphatemic rickets OrphaNet|UMLS|HPO|MalaCards C1961131 Cough adverse event C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C4085211 Pain distress question C0020507 Hyperplasia HSDN C0026821 Cramp C0004936 Mental disorders HSDN C0522224 Palsied C0026269 Mitral valve stenosis HSDN C1963177 Muscle pain adverse event C0026205 Miosis disorder MalaCards C0401149 Constipation chronic C1531773 Currarino triad MalaCards|HPO|UMLS C4084774 Have weight loss C0162872 Aortic aneurysm, thoracic HSDN C0013362 Dysarthrias C0796204 Worster-drought syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C0268228 Neuraminidase 1 deficiency HPO C0018991 Paralysis one side of body C0039590 Testicular neoplasms HSDN C0520909 Ponv C0022661 Kidney failure, chronic HSDN C4084769 Vomiting frequency C0029184 Orbital fracture HSDN C0037763 Spasm C0006109 Brain damage, chronic HSDN C0013404 Respiratory difficulty C0030290 Fistula pancreatic HSDN C0007758 Cerebellar ataxia C2827407 Infectious otitis media HSDN C2984058 Have pain C0037397 Behavior social HSDN C3815497 Cough C0917875 Esophageal diverticulosis HSDN C4084724 Usual severity constipation C0039614 Tetanus HSDN C3898969 Have been vomiting C0021783 Internal external locus of control HSDN C3641756 Have diarrhea C0016627 Avian influenza DiseaseOntology|HSDN|MalaCards C0036572 Convulsion C0021831 Intestinal diseases HSDN C4084768 Usual severity vomiting C0004364 Autoimmune diseases HSDN C4084726 Distress cough C0036231 Sarcocystosis DiseaseOntology C4085317 Diarrhea frequency C2937421 Prostatic hyperplasia HSDN C4084897 Sleep disturbance subordinate domain C4048800 Telomeric 22q13 monosomy syndrome MalaCards C0015469 Facial paralysis C0019069 Hemophilia a HSDN C0850758 Pain pelvic C0018965 Hematuria HSDN C0018784 Deafness sensorineural C0037930 Spinal cord neoplasms HSDN C3146279 Coma C0034885 Rectal neoplasms HSDN C0026838 Spasticity muscle C0016563 Form perception HSDN C0221166 Paraparesis C0016548 Foreign body migration HSDN C0034150 Skin purpura C0042138 Uterine neoplasms HSDN C0005745 Blepharoptosis C2713347 7-dehydrocholesterol reductase deficiency OrphaNet|HPO|MalaCards C0017565 Gingiva hemorrhage C0020640 Inherited factor ii deficiency HPO C2203646 Jaundice C0035335 Retinoblastoma HSDN C2242996 Tingling C0154723 Migraine with aura HSDN C0027497 Queasy C0020435 Hyperbilirubinemia, hereditary HSDN C0151686 Growth retardation C4015172 Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay MalaCards C2911645 Weight loss adverse event C0042029 Urinary tract infection HSDN C0575081 Abnormal gait C1849811 Pili torti and developmental delay OrphaNet|MalaCards C0036572 Convulsion C0342705 Folate malabsorption, hereditary OrphaNet|UMLS|HPO|MalaCards C1557397 Adverse event associated with pain C0206655 Alveolar rhabdomyosarcoma HSDN C4085317 Diarrhea frequency C1299262 Sarcoma - category (morphologic abnormality) HSDN C0015469 Facial paralysis C0006131 Branchioma HSDN C0030193 Sense of pain C0020433 Hyperbilirubinemia HSDN C0242936 Center pain C0013336 Dwarfism HSDN C2315100 Pediatric failure to thrive C0008924 Cleft lip HSDN C3887873 Hearing loss C0038356 Stomach neoplasms HSDN C0149793 Transient monocular blindness C2713319 Arylsulfatase a deficiency OrphaNet|MalaCards C1963252 Tremor adverse event C0751803 Brain stem hemorrhage, post traumatic HSDN C0007758 Cerebellar ataxia C0021295 Infant, premature, diseases HSDN C2233629 Orange eyelid growth C0015424 Eyelid neoplasms UMLS C0042571 Vertigo subjective C0152171 Idiopathic pulmonary hypertension OrphaNet C0349506 Sun sensitivity C0175694 Smith-lemli-opitz syndrome OrphaNet|HPO|MalaCards C2024893 Cardiovascular surgery result: fatigue C0015457 Expression facial HSDN C4085210 Usual severity pain C0270327 Bedwetting HSDN C0013604 Edematous C1532560 Plasmacytoma - category HSDN C0000727 Abdomen acute C0026266 Mitral valve insufficiency HSDN C0012569 Double vision C0001432 Adenoma, chromophobe HSDN C0034150 Skin purpura C0272295 Purpura, rheumatica MalaCards C3641756 Have diarrhea C1306577 Dies patient HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0460137 Push down or depress HSDN C0013428 Painful urination C0009770 Conjunctivitis, chlamydia HSDN C4042891 Sleep wake disorders C0017563 Gingival diseases HSDN C0037763 Spasm C0236969 Substance-related disorders HSDN C0020673 Hypothermia (central) (local) C0003467 Anxiety HSDN C0518090 Frequency of pain question C0020507 Hyperplasia HSDN C0019209 Large liver C0019034 Hemoglobin sc disease MalaCards C4085317 Diarrhea frequency C0268416 Enterokinase deficiency MalaCards|HPO C0018681 Headache, cephalalgia C4029298 Ergotamine induced headache with intractable headache UMLS C1836296 Lower extremity weakness C1846046 Spastic paraplegia 16, x-linked (disorder) MalaCards|UMLS C0019572 Hairiness C0271694 Familial partial lipodystrophy HSDN C0850758 Pain pelvic C2984289 Melanoma pathway HSDN C3274924 Have been coughing C0717360 Disease lyme vaccine HSDN C0085642 Asphyxia reticularis C1579830 Cutaneous vesicle HSDN C4084768 Usual severity vomiting C0017536 Giardiasis DiseaseOntology|HSDN C1384666 Decreased hearing C0025294 Meningococcal meningitis HSDN C2024878 Cardiovascular surgery result: dyspnea C1963064 Anxiety adverse event HSDN C0033074 Presbycusis C1384607 Food deprivation HSDN C4084802 Usual severity diarrhea C0409959 Osteoarthritis, knee HSDN C1963063 Anorexia adverse event C2984572 Malaria pathway HSDN C3641755 Have constipation C1961100 Erectile dysfunction adverse event HSDN C2029884 Hearing loss by exam C0796070 Microphthalmia, syndromic 7 MalaCards C0030975 Disorders perception C0022665 Kidney neoplasm HSDN C0028738 Nystagmus C0344559 Irido-corneo-trabecular dysgenesis (disorder) HPO C1962972 Proteinuria adverse event C1858915 Focal segmental glomerulosclerosis 2 HPO C2024893 Cardiovascular surgery result: fatigue C1739094 Foodborne botulism MalaCards C0026821 Cramp C0018565 Acquired deformity of hand, nos HSDN C0013404 Respiratory difficulty C1704436 Peripheral arterial diseases HSDN C0234518 Speech slurred C1848813 Thyrocerebral-retinal syndrome MalaCards C4084768 Usual severity vomiting C0038000 Spleen rupture HSDN C3463815 Feel fatigue C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C4085211 Pain distress question C0019285 Diaphragmatic hernia traumatic HSDN C0009806 Constipate C0796095 Opitz trigonocephaly syndrome MalaCards|HPO C0424755 Fever symptoms C1456660 Monkeypox virus infections MalaCards C4084775 Usual severity weight loss C0024894 Mastitis HSDN C0016199 Pain flank C0027706 Hereditary nephritis HSDN C0018784 Deafness sensorineural C0018798 Congenital heart defects HSDN C3898969 Have been vomiting C0005940 Bone diseases HSDN C1963093 Dizziness adverse event C0029456 Osteoporosis HSDN C4085211 Pain distress question C0028945 Oligodendroglioma HSDN C0020578 Hyperventilate C3888013 Hypnoses HSDN C0036572 Convulsion C0022570 Keratitis dentritic HSDN C0036572 Convulsion C0795825 Chromosome 8, trisomy 8p MalaCards C1963252 Tremor adverse event C0020615 Hypoglycemia HSDN C0242936 Center pain C1510412 Pseudoaneurysm HSDN C0022346 Yellow skin C0549567 Pigmentation disorders HSDN C1963090 Dehydration adverse event C0598226 Harlequin type ichthyosis HPO C0030193 Sense of pain C0040436 Dental erosion HSDN C0015469 Facial paralysis C1881674 Medical device emits smoke HSDN C0014591 Bleeding nose C0032533 Polymyalgia rheumatica MalaCards C0085593 Chill C0014661 Equine infectious anemia MalaCards C4084723 Constipation C1963083 Cholecystitis adverse event HSDN C4084724 Usual severity constipation C0020473 Hyperlipidemia HSDN C1279888 Proteinuria of undiagnosed cause C0030567 Parkinson disease HSDN C1719454 Central hearing loss in both ears C0452138 Sensorineural hearing loss, bilateral UMLS C0042571 Vertigo subjective C0026771 Trauma multiple HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0008372 Intrahepatic cholestasis HSDN C0454644 Delayed language development C2930913 Chromosome 13q deletion MalaCards C0010200 Cough symptom C0026266 Mitral valve insufficiency HSDN C0028961 Urine output decreased C0011570 Mental depression HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036899 Abstinence sex HSDN C4085317 Diarrhea frequency C0023281 Leishmaniasis HSDN C0039070 Collapse fleeting C0011570 Mental depression HSDN C0013604 Edematous C0012644 Animal disease models HSDN C0042798 Vision dim C3542499 Aminoacylase 2 deficiency OrphaNet C0011206 Delirium acute C0024408 Machado-joseph disease HSDN C0000737 Abdomen pain C2984330 Chagas disease pathway HSDN C0036572 Convulsion C2931004 Congenital disorder of glycosylation type 1j OrphaNet|UMLS|HPO|MalaCards C1963137 Hydrocephalus adverse event C3553330 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 MalaCards C3539890 Pelvic pain causes awakening at night C0019310 Hernia, obturator HSDN C0015469 Facial paralysis C0006436 Burning electric HSDN C3814778 Hemolytic index C0019034 Hemoglobin sc disease MalaCards C0240941 Scalp pruritus C1290028 Disease of skin and/or subcutaneous tissue of head UMLS C2364111 Gustatory anesthesia C0032302 Mycoplasma pneumonia HSDN C0002170 Alopecia disorders C1866426 T-cell immunodeficiency, congenital alopecia and nail dystrophy MalaCards|HPO C1959630 Eye pain adverse event C0028840 Ocular hypertension HSDN C2169806 Tic C0020524 Disorders of excessive somnolence HSDN C0026838 Spasticity muscle C3809672 Mental retardation, autosomal recessive 37 UMLS C0008031 Pain chest C0027149 Myxoma HSDN C1384666 Decreased hearing C0221357 Brachydactyly HSDN C0728710 Pupil constriction observed C0023348 Leprosy, lepromatous HSDN C0039070 Collapse fleeting C0004352 Autistic disorder HSDN C0013378 Dysgensia C0015302 External exotoses HSDN C0018780 Frequencies hearing high loss C0001828 Agricultural workers' diseases HSDN C2984058 Have pain C0013386 Dyskinesia, drug-induced HSDN C2911645 Weight loss adverse event C0017205 Gaucher disease HSDN C0033774 Skin pruritus C0020678 Hypotrichosis HSDN C0018784 Deafness sensorineural C1457883 Aggressive reaction HSDN C0013604 Edematous C1856304 Gsd iv, neuromuscular form, congenital MalaCards|HPO C0155552 Hearing loss mixed C0005758 Bulla HSDN C1963184 Nystagmus adverse event C3150802 Myopathy, lactic acidosis, and sideroblastic anemia 2 MalaCards|HPO C0018784 Deafness sensorineural C1876214 Albinoidism, oculocutaneous, autosomal dominant HSDN C4085661 Usual severity nausea C0013274 Patent ductus arteriosus HSDN C0022408 Disorder joint C0268060 Juvenile hemochromatosis OrphaNet|HPO|MalaCards C0027497 Queasy C0020473 Hyperlipidemia HSDN C4085862 Bothered by nausea C2364172 Adherence to medication regime HSDN C0427055 Face weakness C1969785 Muscular dystrophy, limb-girdle, type 2l (disorder) MalaCards|HPO C0033377 Caudal displacement C0795944 Fountain syndrome MalaCards C1549543 Administration method - pain C3714535 Malocclusion, angle class ii HSDN C0009460 Communication impairment C0085092 Parenting behavior HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036130 Salpingitis HSDN C2984058 Have pain C0022578 Keratoconus HSDN C4084773 Bothered by weight gain C0027707 Nephritis, interstitial HSDN C3827868 Tachycardia by ecg finding C0007279 Carotid body paraganglioma HPO C2203646 Jaundice C0017416 Genital neoplasms, female HSDN C0751837 Gait ataxic C0004114 Astrocytoma HSDN C0042963 Symptoms vomiting C0010399 Crying HSDN C0332573 Macula C0398367 Histiocytic necrotizing lymphadenitis MalaCards C4084774 Have weight loss C0036221 Mast-cell sarcoma OrphaNet|MalaCards C1549543 Administration method - pain C0271051 Macular retinal edema HSDN C1971624 Appetite absent C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0518090 Frequency of pain question C0019202 Hepatolenticular degeneration HSDN C2242996 Tingling C0011405 Pulp disorder HSDN C0151786 Weakness muscle C0017178 Gastrointestinal diseases HSDN C1527344 Dysphonia C0220756 Niemann-pick disease, type c OrphaNet C4084897 Sleep disturbance subordinate domain C0221759 Brachial plexus neuritis MalaCards|HPO C0237849 Skin desquamation C0600327 Toxic shock syndrome DiseaseOntology|MalaCards C4084775 Usual severity weight loss C0085409 Polyendocrinopathies, autoimmune HSDN C0020538 Hbp C0026363 Mohr-claussen syndrome MalaCards C4085862 Bothered by nausea C0018939 Hematological disease HSDN C0011991 Loose stools C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0518090 Frequency of pain question C1384607 Food deprivation HSDN C4085210 Usual severity pain C2021655 Transvaginal ultrasound: anencephaly of fetus HSDN C0349588 Stature short C0032339 Rothmund-thomson syndrome OrphaNet|HPO|MalaCards C3898969 Have been vomiting C0268542 Ornithine carbamoyltransferase deficiency HSDN|HPO C0036572 Convulsion C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards|UMLS C0013604 Edematous C0032914 Pre-eclampsia HSDN C0002962 Angina C0597109 Nurse's role HSDN C0018681 Headache, cephalalgia C0026766 Multiple organ failure HSDN C1963087 Constipation adverse event C0020517 Hypersensitivity HSDN C2911645 Weight loss adverse event C0040715 Chromosomal translocation HSDN C0023530 Leukopenia C3553512 Immunodeficiency, common variable, 8, with autoimmunity MalaCards C4042891 Sleep wake disorders C0004361 Autogenic therapy HSDN C1557397 Adverse event associated with pain C0027809 Neurilemmoma MalaCards C0497247 Blood pressure elevation C0029294 Orofaciodigital syndromes MalaCards C0004941 Behavioral symptoms C1845055 Alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked OrphaNet C0015672 Decreased energy C0024788 Green monkey virus disease OrphaNet|MalaCards C0151686 Growth retardation C1857662 Coach syndrome MalaCards|HPO C0270948 Neurogenic muscular atrophy C3150171 Ftld-tdp, tardbp-related HPO C0030552 Paralysis partial C0007682 Cns disorder HSDN C1963180 Neck pain adverse event C0206734 Hemangioblastoma HSDN C1856661 Cornea cloudy C2717836 Steroid sulfatase deficiency disease OrphaNet|HPO|MalaCards C0476457 Senile debility C0036654 Senility, no psychosis UMLS C0040822 D tremors C0005586 Bipolar disorder HSDN C1549543 Administration method - pain C0019880 Homocystinuria HSDN C1279888 Proteinuria of undiagnosed cause C0585442 Osteosarcoma of bone HSDN C0022346 Yellow skin C0004626 Pneumonia, bacterial HSDN C0424755 Fever symptoms C0027660 Neoplasms, glandular and epithelial HSDN C0018991 Paralysis one side of body C0038531 Subclavian artery stenosis HSDN C0013362 Dysarthrias C1837094 Myasthenic syndrome, congenital, ie MalaCards|HPO C0030193 Sense of pain C2073625 X-ray of chest: pleural effusion HSDN C2024893 Cardiovascular surgery result: fatigue C2931542 Shapiro syndrome OrphaNet|MalaCards C0015672 Decreased energy C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0036572 Convulsion C1838121 Acrocardiofacial syndrome MalaCards C0042928 Paralysis vocal cord C0340629 Aortic aneurysm without mention of rupture nos HSDN C0518090 Frequency of pain question C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0398650 Idiopathic thrombocytopenia purpura C0009782 Connective tissue diseases HSDN C0522224 Palsied C0003504 Aortic valve insufficiency HSDN C0349588 Stature short C0342777 Succinate-coenzyme q reductase deficiency MalaCards C4084724 Usual severity constipation C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C4085210 Usual severity pain C0030283 Pancreatic cyst HSDN C3641756 Have diarrhea C0006736 Body stone HSDN C0518090 Frequency of pain question C0020162 Humerus fracture HSDN C1971624 Appetite absent C3273031 Hnec MalaCards C0036572 Convulsion C0268448 Primary hypomagnesemia (disorder) MalaCards|HPO|UMLS C0026884 Muteness C0040517 Gilles de la tourette syndrome HSDN C4084788 Have dizziness C1961100 Erectile dysfunction adverse event HSDN C4084775 Usual severity weight loss C0037928 Spinal cord diseases HSDN C0232461 Increased appetite C0010276 Craniopharyngioma MalaCards|HPO C1963170 Hypothermia adverse event C0027051 Myocardial infarction HSDN C0027066 Myoclonic jerking C0023066 Laryngismus HSDN C0917816 Deficiency mental C2608080 Renal hypoplasia, isolated (disorder) HPO C0424755 Fever symptoms C0040997 Trigeminal neuralgia HSDN C0015468 Face pain C0004623 Bacterial infections HSDN C0013395 Indigestion C0002989 Epithelioid hemangioma of skin HSDN C0040034 Thrombocytopenia C2931850 Aase smith syndrome 2 MalaCards|HPO C2237041 Shox gene with short stature C1865639 Gracile bone dysplasia MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0238190 Inclusion body myositis (disorder) HSDN C3641756 Have diarrhea C1836706 Hyperthyroidism, nonautoimmune MalaCards C1963087 Constipation adverse event C0033578 Prostatic neoplasms HSDN C0003862 Pain joint C0011581 Depressive disorder HSDN C0848203 Male pelvic pain C1546602 Specimen source codes - diverticulum HSDN C0917816 Deficiency mental C0265425 9p partial monosomy syndrome OrphaNet|MalaCards C0018991 Paralysis one side of body C0270805 Cerebral hemiplegic palsy UMLS C0000737 Abdomen pain C3146253 Stage iii rectal cancer ajcc v7 UMLS C1963065 Apnea adverse event C1962986 Glaucoma adverse event HSDN C4084774 Have weight loss C0007117 Basal cell carcinoma HSDN C0015672 Decreased energy C0017205 Gaucher disease OrphaNet|MalaCards C0037316 Not enough sleeping C0035435 Rheumatism HSDN C0349506 Sun sensitivity C2677889 Protoporphyria, erythropoietic, x-linked dominant MalaCards|HPO C0151686 Growth retardation C1847013 Nephronophthisis 4 MalaCards|HPO C0031911 Pigment deposition C1838571 Ceroid lipofuscinosis, neuronal, 7 MalaCards C0085128 Cardiac output elevated C0001125 Acidosis, lactic HSDN C0494475 Seizure generalized tonic clonic C2930815 Acute cerebral gaucher disease MalaCards C0020505 Excessive eating C3809877 Schaaf-yang syndrome MalaCards C0751837 Gait ataxic C3809327 Spinocerebellar ataxia, autosomal recessive 14 MalaCards|UMLS C0011991 Loose stools C0008497 Choriocarcinoma HSDN C4085222 Nausea C0020550 Hyperthyroidism HSDN C0030552 Paralysis partial C0040809 Patient refusal of treatment HSDN C1549543 Administration method - pain C0008350 Cholelithiasis HSDN C0003467 Angst C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C1963252 Tremor adverse event C0031154 Peritonitis HSDN C1549543 Administration method - pain C0029184 Orbital fracture HSDN C0024031 Back pain lower back C0009450 Disease caused by microorganism HSDN C2203646 Jaundice C0027932 Neurotic disorders HSDN C0043094 Weight gain C0000768 Congenital abnormality HSDN C0393588 Dystonias paroxysmal C1847501 Glut1 deficiency syndrome MalaCards|UMLS C0234132 Pyramidal sign C2931821 Nakamura osame syndrome MalaCards C0030552 Paralysis partial C3714932 Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 MalaCards C0020450 Hyperemesis gravidarum C0860549 Refeed syndrome HSDN C3815497 Cough C2984572 Malaria pathway HSDN C0522224 Palsied C0018671 Head and neck neoplasms HSDN C4084769 Vomiting frequency C1299919 Enteric coccidiosis HSDN C0009421 Comatose C0019195 Hepatitis, viral, human HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0026936 Mycoplasma infections HSDN C4084784 Diarrhea C0206698 Cholangiocarcinoma HSDN C0233565 Bradykinesia C0038868 Progressive supranuclear palsy OrphaNet|HPO|UMLS C0000737 Abdomen pain C0041755 Adverse reaction to drug HSDN C0013421 Dystonia C0020538 Hypertensive disease HSDN C0518090 Frequency of pain question C0020120 Engineering humans HSDN C3274924 Have been coughing C0029342 Orthomyxoviridae infections HSDN C0034150 Skin purpura C1532560 Plasmacytoma - category HSDN C0243026 Generalized infection C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C3887873 Hearing loss C0042018 Urinary calculi HSDN C0012833 Dizzy C1090821 Sepsis (invertebrate) HSDN C0027796 Neuralgias C0220981 Metabolic acidosis HSDN C3641756 Have diarrhea C0031542 Phlebitis HSDN C0013362 Dysarthrias C0004623 Bacterial infections HSDN C0424755 Fever symptoms C0029882 Otitis media HSDN C0007758 Cerebellar ataxia C1836474 Spinocerebellar ataxia, autosomal recessive 7 MalaCards|UMLS C2926613 Chest pain:finding:point in time:^patient:ordinal C1579931 Depressed - symptom HSDN C0241210 Speaking delay C2751843 Leukoencephalopathy, cystic, without megalencephaly MalaCards|HPO C0232461 Increased appetite C0021670 Insulinoma OrphaNet|HPO|MalaCards C0085636 Light sensitivity C2931258 Amaurosis congenita of leber, type 1 MalaCards|HPO|UMLS C0011991 Loose stools C1546654 Specimen source codes - granuloma HSDN C1549543 Administration method - pain C0008519 Ectopic tissue HSDN C0012833 Dizzy C0028796 Dermatitis, occupational HSDN C0030193 Sense of pain C0596263 Carcinogenesis HSDN C0042384 Vasculitis, nonspecific C0343208 Essential mixed cryoglobulinemia OrphaNet|MalaCards C2919142 Short stature adverse event C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C0018991 Paralysis one side of body C0022865 Obstetric labor complications HSDN C0018808 Murmur C3542024 Aortic valve disease 2 MalaCards C0557874 Global developmental delay C0795887 Chromosome xp21 deletion syndrome MalaCards C0750394 Wbc low C0342705 Folate malabsorption, hereditary MalaCards|HPO C0000737 Abdomen pain C0018206 Granulosa cell tumor HSDN C4085210 Usual severity pain C0338437 Neurocysticercosis HSDN C0011991 Loose stools C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C0242936 Center pain C0005686 Urinary bladder diseases HSDN C0023380 Lethargy C0162677 Caliciviridae infections HSDN C0027498 Nausea vomiting C0017181 Gastrointestinal hemorrhage UMLS C4084776 Weight loss C0030809 Pemphigus vulgaris OrphaNet|MalaCards C0242936 Center pain C0018553 Hamartoma syndrome, multiple HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085073 Prosthesis-related infection HSDN C0034933 Abnormal reflexes C0162703 Pain sensitivity HSDN C1962972 Proteinuria adverse event C0220989 Acquired partial lipodystrophy MalaCards|HPO C1963164 Lymphopenia adverse event C3809768 Immunodeficiency 13 MalaCards C0019214 Hepatosplenomegaly C0566602 Primary sclerosing cholangitis OrphaNet|HPO|MalaCards C0030193 Sense of pain C0038536 Subcutaneous emphysema HSDN C0026821 Cramp C0011265 Presenile dementia HSDN C4084768 Usual severity vomiting C0042870 Vitamin d deficiency HSDN C2911647 Weight gain adverse event C0016053 Fibromyalgia HSDN C0026826 High muscle tone C1836669 Congenital disorder of glycosylation, type if MalaCards|HPO C0042571 Vertigo subjective C3887678 Cpnet MalaCards C0007758 Cerebellar ataxia C0029534 Other cerebellar ataxia MalaCards|UMLS C0013604 Edematous C0032343 Poisoning HSDN C1963091 Diarrhea adverse event C0021890 Intraoperative complications HSDN C4084766 Vomiting C0032965 Pregnancy complications, infectious HSDN C0085636 Light sensitivity C0338395 Escherichia coli meningitides HSDN C4084768 Usual severity vomiting C0009450 Disease caused by microorganism HSDN C1963281 Vomiting adverse event C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C4085210 Usual severity pain C0024143 Lupus nephritis HSDN C0030193 Sense of pain C0001206 Acromegaly HSDN C4085210 Usual severity pain C0030271 Pancoast syndrome HSDN C0007758 Cerebellar ataxia C0024115 Lung diseases HSDN C4085549 Dizziness C0022701 Kinesthesia HSDN C1963087 Constipation adverse event C0031212 Personality disorders HSDN C0150055 Pain chronic C1719393 Chronic pain due to trauma UMLS C2096293 Ent surgical result ear vertigo C0042338 Herpesvirus 3, human HSDN C3641756 Have diarrhea C0006261 Bronchial diseases HSDN C0013404 Respiratory difficulty C0038395 Streptococcal infections HSDN C4084784 Diarrhea C0016667 Fragile x syndrome HSDN C4084767 Bothered by vomiting C0022661 Kidney failure, chronic HSDN C0004134 Dyssynergia C0022541 Kearns-sayre syndrome OrphaNet|HPO|MalaCards C0041105 Jaw spasm C0036344 Schizophrenia, catatonic HSDN C0231835 Respiration rate increased C0233315 Premature birth of newborn HSDN C0030486 Extremity paralysis, lower C0019557 Hip fx HSDN C1963184 Nystagmus adverse event C1866282 Ceroid lipofuscinosis, neuronal, 6 MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0004239 Atrial flutter HSDN C0848203 Male pelvic pain C0004275 Attitude health HSDN C0413252 Hypothermia due to exposure C2937421 Prostatic hyperplasia HSDN C0028738 Nystagmus C2750220 Karak syndrome MalaCards|HPO C1963281 Vomiting adverse event C0017574 Gingivitis HSDN C0037384 Snore C4050613 Anxiety scale (basc-2) HSDN C4084768 Usual severity vomiting C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0857305 Thrombocytopenia purpura C0221752 Rbc urine HSDN C1557397 Adverse event associated with pain C0018206 Granulosa cell tumor HSDN C0020672 Body temperature decreased C0037274 Dermatologic disorders HSDN C0024032 Birth weight subnormal C0342284 Bangstad syndrome MalaCards C1963252 Tremor adverse event C0007795 Diffuse cerebral sclerosis of schilder HSDN C0003962 Ascites C1838120 Hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities OrphaNet|MalaCards C0009763 Conjunctiva inflammation C0268138 Xeroderma pigmentosum, complementation group d HPO C4085548 Usual severity dizziness C1510412 Pseudoaneurysm HSDN C0231528 Muscle pain generalized C0220679 Ehlers-danlos syndrome, autosomal dominant, type unspecified OrphaNet C0000727 Abdomen acute C0010636 Papillary cystadenoma HSDN C0424755 Fever symptoms C0005830 Blood protein disorders HSDN C0037771 Paraparesis spastic C0023264 Leigh disease HSDN C0009806 Constipate C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C3539891 Pelvic pain to the rear C0012979 Canine disease HSDN C0043094 Weight gain C0795623 Hepatitis a vaccine, inactivated HSDN C0037763 Spasm C0700095 Central neuroblastoma HSDN C0007166 Cardiac output decreased C0001175 Acquired immunodeficiency syndrome HSDN C3274924 Have been coughing C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0151786 Weakness muscle C1419869 Scnn1b gene HSDN C0151786 Weakness muscle C0021295 Infant, premature, diseases HSDN C4084727 Cough frequency C1547044 Kind of quantity - smell HSDN C3829611 Nausea frequency C1253937 Pericardial effusion HSDN C3665347 Vision impaired C2931277 Pena shokeir syndrome type 2 OrphaNet|HPO|MalaCards C0520909 Ponv C0344434 Atrial fibrillation ecg HSDN C3665386 Abnormal vision C1857277 Donnai-barrow syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0025268 Multiple endocrine neoplasia type 2a OrphaNet C0518090 Frequency of pain question C0020179 Huntington disease HSDN C0013405 Dyspnea, paroxysmal C0037199 Sinusitis HSDN C0037763 Spasm C0010346 Crohn disease HSDN C4085210 Usual severity pain C0011989 Camurati-engelmann syndrome HSDN C0424755 Fever symptoms C0021841 Intestinal neoplasms HSDN C0521483 Mucous hyperplasia C0267018 Irritative hyperplasia of oral mucosa UMLS C0042024 Urine incontinence C0036202 Sarcoidosis HSDN C0751401 Ophthalmoparesis C1837094 Myasthenic syndrome, congenital, ie MalaCards|HPO C0026826 High muscle tone C0018801 Heart failure HSDN C4084774 Have weight loss C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4020887 Photodysphoria C1868569 Patterned dystrophy of retinal pigment epithelium MalaCards|HPO C4085549 Dizziness C0033054 Prenatal exposure delayed effects HSDN C2169806 Tic C0014544 Epilepsy HSDN C1963064 Anxiety adverse event C0795907 Conotruncal anomaly face syndrome MalaCards|HPO C0009806 Constipate C0003873 Rheumatoid arthritis HSDN C1963281 Vomiting adverse event C1283620 Sucrase-isomaltase deficiency, congenital OrphaNet|MalaCards C3641756 Have diarrhea C0020732 Iatrogenic disease HSDN C0015230 Exanthem C3714602 Staphylococcal toxic shock syndrome MalaCards C0026838 Spasticity muscle C0085621 Spastic paralysis UMLS C0019825 Voice hoarseness C0278727 Small cell lung cancer recurrent UMLS C0020649 Blood pressure decreased C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0238551 Abdomen llq pain C0392525 Nephrolithiasis UMLS C0018681 Headache, cephalalgia C0751304 Meningioma, parasagittal UMLS C0406671 Burning scrotum C1302834 Disorder of skin of trunk UMLS C0013404 Respiratory difficulty C0009319 Colitis HSDN C2237041 Shox gene with short stature C0220767 Craniofrontonasal dysplasia HPO C0005745 Blepharoptosis C3806742 Colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation MalaCards C0542476 Forgetful C0036421 Systemic scleroderma MalaCards C0011168 Disorder deglutition C1837329 Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema MalaCards C0742857 Cough acute C0740767 Resp_tract problem UMLS C4084769 Vomiting frequency C1416865 Lipa gene HPO C3146279 Coma C0919267 Ovarian neoplasm HSDN C0009676 Confusion state C0010709 Cyst HSDN C0587047 Mass of trunk C0341225 Gastric hamartoma UMLS C0018808 Murmur C0001418 Adenocarcinoma HSDN C4085862 Bothered by nausea C1456781 Benign melanocytic nevus HSDN C0026961 Pupil dilated C0220633 Uveal melanoma HPO C1000483 Genus anemia C2931850 Aase smith syndrome 2 OrphaNet|MalaCards C1963137 Hydrocephalus adverse event C0003803 Arnold chiari malformation MalaCards C0577567 Mass of urogenital structure C0268781 Idiopathic granulomatous interstitial nephropathy, nos UMLS C1963170 Hypothermia adverse event C0032343 Poisoning HSDN C3887638 Failure to thrive in infant C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C1963252 Tremor adverse event C0344434 Atrial fibrillation ecg HSDN C4042891 Sleep wake disorders C0021655 Insulin resistance HSDN C3641755 Have constipation C0149573 Structure of posterior inferior cerebellar artery HSDN C0036572 Convulsion C3501891 Mitochondrial dna depletion myopathy, autosomal recessive MalaCards C3641755 Have constipation C0010695 Cystocele HSDN C0012833 Dizzy C1707400 Classic medulloblastoma MalaCards C3829611 Nausea frequency C0004442 Avoidance learning HSDN C0015672 Decreased energy C0019348 Herpes simplex infections HSDN C0043094 Weight gain C0037275 Skin diseases, vesiculobullous HSDN C0522224 Palsied C3714509 Nutrition disorders HSDN C0042963 Symptoms vomiting C0035235 Respiratory syncytial virus infections HSDN C0018784 Deafness sensorineural C0796204 Worster-drought syndrome MalaCards C0019209 Large liver C0026272 Mixed connective tissue disease MalaCards C0041105 Jaw spasm C4049644 Depression HSDN C0241210 Speaking delay C1959582 Pten hamartoma tumor syndrome MalaCards C1963063 Anorexia adverse event C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C2364111 Gustatory anesthesia C0043065 Water electrolyte imbalance HSDN C0013404 Respiratory difficulty C3280574 Surfactant metabolism dysfunction, pulmonary, 5 MalaCards|UMLS C4042891 Sleep wake disorders C0270853 Myoclonic epilepsy, juvenile HSDN C0042963 Symptoms vomiting C1553188 Hemolysis - observation HSDN C1963281 Vomiting adverse event C0062527 Hepatitis b vaccine HSDN C0008031 Pain chest C0029408 Degenerative polyarthritis HSDN|UMLS C4084724 Usual severity constipation C0042769 Virus diseases HSDN C0013528 Echo speech C0009651 Conditioning operant HSDN C0015672 Decreased energy C0585216 Alpha-thalassemia myelodysplasia syndrome OrphaNet|HPO C0013404 Respiratory difficulty C0020255 Hydrocephalus HSDN C4084802 Usual severity diarrhea C1261470 Congenital meningocele HSDN C0018926 Emesis bloody C0014848 Esophageal achalasia HSDN C2911647 Weight gain adverse event C0220847 C hepatitis virus HSDN C0042798 Vision dim C0152136 Low tension glaucoma HSDN C1963252 Tremor adverse event C1522133 High cholesterol level HSDN C0040822 D tremors C0042812 Acuity visual HSDN C0039231 Heartbeats increased C0162532 Variegate porphyria MalaCards|HPO C0085636 Light sensitivity C0524812 Intracranial hypotension HSDN C0019572 Hairiness C0453996 Tobacco smoking HSDN C0497247 Blood pressure elevation C1857554 Hsd11b2, arg213cys HPO C0349506 Sun sensitivity C1857338 Deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy MalaCards C0576456 Poor feeding C3553449 Pontocerebellar hypoplasia, type 1b MalaCards C2024893 Cardiovascular surgery result: fatigue C0342337 Insulin resistance syndrome, type b OrphaNet|MalaCards C4042891 Sleep wake disorders C0003493 Aortic diseases HSDN C0039070 Collapse fleeting C0349604 Intracranial meningioma MalaCards C4085210 Usual severity pain C0014457 Eosinophilia HSDN C0520966 Coordination impaired C1864112 Huntington disease-like 1 MalaCards|HPO|UMLS C4085211 Pain distress question C0024221 Lymphangioma HSDN C0041657 Consciousness loss C0314657 Genetic predisposition HSDN C0030554 Abnormal sensation C0238417 Scorpion sting HSDN C0029163 Hemorrhage mouth C0022363 Jaw fracture HSDN C4042891 Sleep wake disorders C0524620 Metabolic syndrome x HSDN C0242936 Center pain C0242658 Homosexuality male HSDN C3539890 Pelvic pain causes awakening at night C3178770 Nutcracker syndrome, renal HSDN C0036572 Convulsion C3806634 Deafness, dystonia, and cerebral hypomyelination MalaCards C0242936 Center pain C1270972 Mild cognitive disorder HSDN C0004134 Dyssynergia C0014859 Esophageal neoplasms HSDN C0010263 Cramp, limb C3538999 Dystonia 23 MalaCards|UMLS C2024878 Cardiovascular surgery result: dyspnea C3714514 Infection HSDN C0011991 Loose stools C0264766 Rheumatic mitral stenosis HSDN C0424755 Fever symptoms C0040761 Transposition of great vessels HSDN C4084724 Usual severity constipation C3280479 Pitt-hopkins-like syndrome 2 MalaCards C3714552 Strength decreased C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C0020455 Hypergammaglobulinemia C0236969 Substance-related disorders HSDN C0005745 Blepharoptosis C1853490 22q13.3 deletion syndrome OrphaNet|HPO|MalaCards C0011991 Loose stools C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C0030486 Extremity paralysis, lower C3146297 Study of behavior during childhood HSDN C0018524 Hallucinate C1555865 Forensic psychiatry HSDN C1527344 Dysphonia C0027743 Nerve compression syndrome HSDN C3641755 Have constipation C1263846 Attention deficit hyperactivity disorder HSDN C0003862 Pain joint C2930851 Intestinal lipophagic granulomatosis OrphaNet|MalaCards C0026826 High muscle tone C1851708 Encephalopathy, recurrent, of childhood MalaCards C4084766 Vomiting C1859499 3-methylcrotonyl coa carboxylase 2 deficiency MalaCards C0086565 Liver function abnormal C1866259 Peroxisome biogenesis disorder, complementation group 13 MalaCards C1384666 Decreased hearing C0037315 Sleep apnea syndromes HSDN C0011991 Loose stools C0740842 Aids related illness UMLS C0005745 Blepharoptosis C0015708 Fazio londe syndrome MalaCards|HPO C1963170 Hypothermia adverse event C0270726 Alexander disease OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0346109 Malignant mesothelioma of peritoneum MalaCards C4084774 Have weight loss C0032131 Plasmacytoma HSDN C1963071 Back pain adverse event C0221013 Mastocytosis, systemic HSDN C0149793 Transient monocular blindness C0751587 Cadasil syndrome OrphaNet|HPO C4084776 Weight loss C0022602 Actinic keratosis HSDN C1836296 Lower extremity weakness C1858106 Spastic paraplegia 12, autosomal dominant (disorder) MalaCards|HPO|UMLS C0878773 Bladder hyperactive C0342257 Complications of diabetes mellitus HSDN C0015672 Decreased energy C0085762 Alcohol abuse UMLS C4084775 Usual severity weight loss C0006309 Brucellosis HSDN C0518090 Frequency of pain question C0037355 Smallpox vaccines HSDN C3641756 Have diarrhea C0005417 Bile duct fistula HSDN C0917816 Deficiency mental C0475813 Alpha thalassemia-mental retardation syndrome OrphaNet|HPO|MalaCards C0023015 Language handicap C0265216 X-linked hydrocephalus syndrome MalaCards C4084774 Have weight loss C0453996 Tobacco smoking HSDN C2984058 Have pain C0021432 Infratentorial neoplasms HSDN C0018991 Paralysis one side of body C0278113 Hemiplegia, spinal UMLS C4084775 Usual severity weight loss C0870082 Hyperkeratosis HSDN C4084802 Usual severity diarrhea C0011616 Contact dermatitis HSDN C0542476 Forgetful C0027145 Myxedema MalaCards C0013604 Edematous C0700208 Acquired scoliosis HSDN C0022346 Yellow skin C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C3463815 Feel fatigue C0035579 Rickets HSDN C2919142 Short stature adverse event C1510479 Neuralgic amyotrophy MalaCards|HPO C0001825 Agraphia C4041080 Neurocognitive disorders HSDN C0042024 Urine incontinence C0027626 Neoplasm invasiveness HSDN C0026838 Spasticity muscle C0796126 Aicardi-goutieres syndrome 1 MalaCards|HPO C0242936 Center pain C0035457 Rhinitis, allergic, perennial HSDN C4085317 Diarrhea frequency C0001727 Afferent loop syndrome HSDN C0015672 Decreased energy C0003496 Aortic rupture HSDN C1963071 Back pain adverse event C0702166 Acne HSDN C3641755 Have constipation C0026650 Movement disorders HSDN C1962972 Proteinuria adverse event C0007682 Cns disorder HSDN C1963087 Constipation adverse event C0020295 Hydronephrosis HSDN C0010200 Cough symptom C0023786 Mucopolysaccharidosis i OrphaNet C3887638 Failure to thrive in infant C1275081 Cardio-facio-cutaneous syndrome HPO C3539022 Pelvic pain decreasing in severity C0037286 Skin neoplasms HSDN C3274924 Have been coughing C0026848 Myopathy HSDN C0013604 Edematous C0037421 Social isolation HSDN C4084774 Have weight loss C0026936 Mycoplasma infections HSDN C4084769 Vomiting frequency C0011603 Dermatitis HSDN C0015672 Decreased energy C0014544 Epilepsy HSDN C0006370 Bulimia C0019693 Hiv infections HSDN C0004134 Dyssynergia C1859566 Bardet-biedl syndrome 8 HPO C0030794 Pelvis pain C0006118 Brain neoplasms HSDN C0013362 Dysarthrias C1847501 Glut1 deficiency syndrome OrphaNet|MalaCards C0030200 Intractable pain C0006663 Calcinosis HSDN C1145670 Failure respiratory C0018522 Hallermann's syndrome MalaCards C0039070 Collapse fleeting C0008519 Ectopic tissue HSDN C2984058 Have pain C0027658 Neoplasms, germ cell and embryonal HSDN C0152447 Urethra discharge C0042075 Urologic diseases UMLS C4084774 Have weight loss C0033871 Psychiatric status rating scales HSDN C0036396 Sciatica C0037286 Skin neoplasms HSDN C3887873 Hearing loss C0028768 Obsessive-compulsive disorder HSDN C0035229 Respiratory function impaired C1266101 Thymic epithelial tumor OrphaNet C4085222 Nausea C3536715 Aa amyloidosis MalaCards C0022346 Yellow skin C1335258 Pretext stage 4 hepatoblastoma UMLS C0020580 Decreased sensation C0026976 Myelitis, transverse HSDN C3539893 Pelvic pain occurs with intercourse C0085096 Peripheral vascular diseases HSDN C0151889 Reflexes tendon increased C0796272 Brooks syndrome MalaCards C0015468 Face pain C0009244 Behavioral cognitive therapy HSDN C3829611 Nausea frequency C0030330 Panniculitis, peritoneal HSDN C0007859 Pain neck C1963178 Myelitis adverse event HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0007193 Cardiomyopathy, dilated HSDN C0042928 Paralysis vocal cord C1963138 Hypertension adverse event HSDN C0151786 Weakness muscle C0795623 Hepatitis a vaccine, inactivated HSDN C4084774 Have weight loss C0035335 Retinoblastoma HSDN C1963252 Tremor adverse event C0018767 Auditory sense HSDN C1963091 Diarrhea adverse event C0032344 Poisoning aspects HSDN C0037763 Spasm C0035302 Retinal artery occlusion HSDN C4085222 Nausea C0008049 Chicken pox DiseaseOntology|HSDN|MalaCards C0424755 Fever symptoms C0494039 Gastrointestinal tularaemia MalaCards C2919142 Short stature adverse event C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0011168 Disorder deglutition C0410226 Congenital myotonic dystrophy MalaCards C1069915 Vertigo C1000483 Genus anemia HSDN C0036572 Convulsion C0013377 Dysgerminoma HSDN C0011991 Loose stools C0019911 Hookworm infections HSDN C0036572 Convulsion C0037997 Splenic diseases HSDN C0030193 Sense of pain C1333472 Adenocarcinoma of ethmoid sinus UMLS C0349588 Stature short C1857339 Deafness, congenital, with vitiligo and achalasia MalaCards C4084768 Usual severity vomiting C0009319 Colitis HSDN C2911645 Weight loss adverse event C0037939 Spinal neoplasms HSDN C3463815 Feel fatigue C0035078 Kidney failure HSDN C0040264 Ear ringing sound C0034929 Reflex HSDN C0034150 Skin purpura C0017416 Genital neoplasms, female HSDN C0018681 Headache, cephalalgia C0278952 Nasopharyngeal cancer recurrent UMLS C4085210 Usual severity pain C1956418 Torsion abnormality HSDN C0041667 Low weight C2751878 Hadziselimovic syndrome MalaCards C4084723 Constipation C1963198 Pancreatitis adverse event HSDN C0242936 Center pain C0162309 Adrenoleukodystrophy HSDN C0042798 Vision dim C0339085 Blepharochalasis, struma, double lip syndrome OrphaNet|MalaCards C0027066 Myoclonic jerking C0033860 Psoriasis HSDN C0520587 Vulvovaginal discomfort C0859003 Vulva feeling swollen UMLS C0042571 Vertigo subjective C0027804 Fatigue neurosis HSDN C0005745 Blepharoptosis C0520719 Spinopontine atrophy MalaCards C0039070 Collapse fleeting C0034530 Injury radiation HSDN C0024031 Back pain lower back C0949760 Personal autonomy HSDN C0042571 Vertigo subjective C0025149 Medulloblastoma MalaCards C0023012 Delay language C0553586 Cafe-au-lait macules with pulmonary stenosis MalaCards C1557397 Adverse event associated with pain C0036875 Disorders of sex development HSDN C2024893 Cardiovascular surgery result: fatigue C0009395 Color perception HSDN C0518090 Frequency of pain question C0235032 Neurotoxicity syndromes HSDN C0011991 Loose stools C0205788 Histiocytoid hemangioma HSDN C0151686 Growth retardation C3150802 Myopathy, lactic acidosis, and sideroblastic anemia 2 MalaCards|HPO C0039070 Collapse fleeting C0018814 Heart rupture, post-infarction HSDN C4084767 Bothered by vomiting C0751273 Infantile globoid cell leukodystrophy MalaCards C2984058 Have pain C0043246 Laceration HSDN C0037316 Not enough sleeping C0282507 Heat stress disorders HSDN C0009421 Comatose C1838979 Mitochondrial complex i deficiency MalaCards|HPO C1963067 Atrial fibrillation adverse event C1833236 Cardiomyopathy, familial hypertrophic, 6 (disorder) HPO C0003467 Angst C0027873 Neuromyelitis optica MalaCards C0030193 Sense of pain C0018816 Heart septal defects HSDN C0013604 Edematous C0037047 Sibling HSDN C0035229 Respiratory function impaired C0796176 Stuve-wiedemann syndrome HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011609 Drug eruptions HSDN C2984058 Have pain C0004045 Asphyxia neonatorum HSDN C0005779 Clotting C1842836 Congenital disorder of glycosylation, type ii MalaCards|HPO C0026821 Cramp C0007820 Cerebrovascular disorders HSDN C4085211 Pain distress question C0006413 Burkitt lymphoma HSDN C0018834 Brash C0282644 Smith-lemli-opitz syndrome, type ii MalaCards|HPO C4085862 Bothered by nausea C0033873 Psychiatry HSDN C0151786 Weakness muscle C0241158 Cicatrix skin HSDN C1549543 Administration method - pain C0019655 Histoplasmosis HSDN C0012833 Dizzy C0027627 Neoplasm metastasis HSDN C0003862 Pain joint C0041296 Tuberculosis HSDN C0013390 Cramps menstrual C0038436 Post-traumatic stress disorder HSDN C4085642 Level of joint stiffness C2350233 Antley-bixler syndrome phenotype MalaCards C0085602 Polydypsia C3245525 Familial renal glucosuria MalaCards C4084802 Usual severity diarrhea C0012819 Diverticular disease of colon HSDN C4085317 Diarrhea frequency C0001621 Adrenal gland diseases HSDN C1963071 Back pain adverse event C0085435 Arthritis, reactive MalaCards C0015469 Facial paralysis C0161409 Cochlear nerve damage HSDN C2138384 Craving earth or clay C0031873 Pica disease UMLS C2984058 Have pain C0024954 Maxillary neoplasms HSDN C0018784 Deafness sensorineural C0027627 Neoplasm metastasis HSDN C0848203 Male pelvic pain C0796561 Melanoma vaccines HSDN C0015469 Facial paralysis C0033324 Prognathism HSDN C4085210 Usual severity pain C0018789 Cardiac aneurysm HSDN C2911645 Weight loss adverse event C0848377 Trauma to the abdomen HSDN C0019825 Voice hoarseness C1518730 Ovarian sertoli-leydig cell tumor with heterologous elements UMLS C0428977 Pulse rate decrease C4015695 Long qt syndrome 15 MalaCards C0012833 Dizzy C1704436 Peripheral arterial diseases HSDN C4085548 Usual severity dizziness C3714514 Infection HSDN C1963087 Constipation adverse event C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C0242936 Center pain C0030318 Panic state HSDN C0010520 Skin cyanosis C0043168 Whooping cough due to unspecified organism HSDN C1963170 Hypothermia adverse event C0026769 Multiple sclerosis HSDN C4085222 Nausea C1302282 Chromaffin cell neoplasm MalaCards C0042798 Vision dim C0038356 Stomach neoplasms HSDN C0002963 Angina variant C2586211 Thrombosis of blood vessel HSDN C0043094 Weight gain C0000786 Spontaneous abortion HSDN C0042571 Vertigo subjective C0155504 Labyrinthitis serous UMLS C4084726 Distress cough C0037939 Spinal neoplasms HSDN C0162835 Hypopigmentation C2931669 Chromosome 8, mosaic trisomy MalaCards C3539896 Pelvic pain occurs with urination C1456865 Ureteral calculi HSDN C1557397 Adverse event associated with pain C0019021 Hemoglobin c disease HSDN C3815497 Cough C0019195 Hepatitis, viral, human HSDN C1963093 Dizziness adverse event C0029877 Ear inflammation HSDN C0018808 Murmur C4085311 Depression - recess HSDN C3887873 Hearing loss C1963274 Vasculitis adverse event HSDN C0264611 Apraxia of speech C3806402 Epilepsy, focal, with speech disorder and with or without mental retardation MalaCards C1971624 Appetite absent C0003838 Arterial occlusive diseases HSDN C1963252 Tremor adverse event C0878578 Orthostatic tremor primary OrphaNet|MalaCards C0020578 Hyperventilate C0520946 Emotional hypersensitivity HSDN C0026838 Spasticity muscle C0751587 Cadasil syndrome OrphaNet|HPO C0037763 Spasm C0023119 Lathyrism HSDN C0027796 Neuralgias C0162820 Dermatitis, allergic contact HSDN C0857305 Thrombocytopenia purpura C0014761 Erythroblastosis, fetal HSDN C4085211 Pain distress question C1636667 Disorder characterized by eosinophilia HSDN C0241210 Speaking delay C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards C0018991 Paralysis one side of body C0023434 Chronic lymphocytic leukemia HSDN C0850758 Pain pelvic C0001418 Adenocarcinoma HSDN C3463815 Feel fatigue C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C4084776 Weight loss C0040128 Thyroid diseases HSDN C2911645 Weight loss adverse event C0023893 Liver cirrhosis, experimental HSDN C3898969 Have been vomiting C0042812 Acuity visual HSDN C4085549 Dizziness C0018944 Hematoma HSDN C0233514 Behavior abnormal C0264743 Rheumatic fever without heart involvement MalaCards C0036572 Convulsion C0022890 Labyrinthine disorder HSDN C0004604 Pain back C0006264 Bronchial neoplasms HSDN C0576456 Poor feeding C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome MalaCards C2984057 Have nausea C0520679 Sleep apnea, obstructive HSDN C0013404 Respiratory difficulty C0878544 Cardiomyopathies UMLS C0497406 Over weight C0020649 Hypotension HSDN C0004134 Dyssynergia C1862441 Ataxia, spastic, with congenital miosis OrphaNet|MalaCards C0023530 Leukopenia C2674723 Ras-associated autoimmune leukoproliferative disorder MalaCards C0522357 Vertigo paroxysmal C1866552 Paragangliomas 2 (disorder) MalaCards C0018784 Deafness sensorineural C0003493 Aortic diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C3501858 Muscular dystrophy, limb-girdle, type 1d MalaCards C3539022 Pelvic pain decreasing in severity C0034065 Pulmonary embolism HSDN C0010200 Cough symptom C0854993 Lung squamous cell carcinoma stage iii UMLS C0000737 Abdomen pain C1136033 Cutaneous mastocytosis OrphaNet|MalaCards C0030554 Abnormal sensation C1510415 Osteosclerotic myeloma MalaCards C4085211 Pain distress question C0036974 Shock HSDN C0008031 Pain chest C0027643 Neoplasm recurrence, local HSDN C0151786 Weakness muscle C0036982 Shock, hemorrhagic HSDN C0023014 Developmental disorder language C0016952 Galactosemias HSDN C0013390 Cramps menstrual C0023890 Liver cirrhosis HSDN C2242996 Tingling C0877172 Hematoma, epidural, spinal HSDN C0860603 Anxiety symptom C0221033 Trisomy x syndrome MalaCards C0013395 Indigestion C0031099 Periodontitis HSDN C1549543 Administration method - pain C0015423 Eyelid diseases HSDN C4084724 Usual severity constipation C3661523 Congenital intestinal aganglionosis OrphaNet|HPO|MalaCards C0917816 Deficiency mental C3810175 Short-rib thoracic dysplasia 10 with or without polydactyly MalaCards C4084725 Usual severity cough C0027889 Hereditary sensory and autonomic neuropathies HSDN C4042891 Sleep wake disorders C1556682 Adverse event associated with infection HSDN C2315100 Pediatric failure to thrive C0268579 Propionic acidemia HPO C0012833 Dizzy C0018944 Hematoma HSDN C0013404 Respiratory difficulty C0009240 Cognition HSDN C0015469 Facial paralysis C3887532 Ulceration HSDN C0018772 Deafness C0010823 Cytomegalovirus infections HSDN C0750394 Wbc low C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C4084774 Have weight loss C0242707 Ventricular dysfunction, right HSDN C1557397 Adverse event associated with pain C0041755 Adverse reaction to drug HSDN C0239574 Fever low grade C0149514 Bronchitis acute DiseaseOntology|MalaCards C0575081 Abnormal gait C0029124 Optic atrophy MalaCards C4084723 Constipation C0600260 Lung diseases, obstructive HSDN C1963170 Hypothermia adverse event C0016542 Foreign body HSDN C2700617 Irritation - emotion C0268689 Vitamin d-dependent rickets, type 1 HPO C0000727 Abdomen acute C0014544 Epilepsy HSDN C0221263 Cafe au lait spot C1855057 Ataxia-telangiectasia variant v2 HPO C0018772 Deafness C0008297 Choanal atresia HSDN C3665347 Vision impaired C1867450 Pseudoxanthoma elasticum, incomplete HPO C3665346 Loss sight C2931588 Gemss syndrome MalaCards C0022346 Yellow skin C0003493 Aortic diseases HSDN C4085549 Dizziness C2239176 Liver carcinoma HSDN C0040034 Thrombocytopenia C0270972 Cornelia de lange syndrome HPO C0011991 Loose stools C0342705 Folate malabsorption, hereditary OrphaNet|UMLS|HPO|MalaCards C4085862 Bothered by nausea C0024115 Lung diseases HSDN C4084776 Weight loss C0017525 Giant cell tumors HSDN C1549543 Administration method - pain C1963084 Colitis adverse event HSDN C1962962 Hyperpigmentation adverse event C1846284 Glucocorticoid deficiency 2 MalaCards C0241210 Speaking delay C1842676 Spinocerebellar ataxia, autosomal recessive 6 (disorder) MalaCards C0026838 Spasticity muscle C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO|UMLS C1145670 Failure respiratory C1848599 Vacterl association with hydrocephalus HPO C0022107 Fussiness C0265498 48, xxxy syndrome MalaCards C0233514 Behavior abnormal C1859298 Spinocerebellar ataxia, autosomal recessive 2 OrphaNet|HPO|MalaCards C0009421 Comatose C0037315 Sleep apnea syndromes HSDN C1963091 Diarrhea adverse event C0004589 B. anthracis HSDN C0035232 Diaphragmatic paralysis C0085655 Polymyositis HSDN C0000737 Abdomen pain C0023801 Lipomatosis HSDN C0853986 Lymphocytes decreased C0043194 Wiskott-aldrich syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0034072 Cor pulmonale HSDN C2919142 Short stature adverse event C1275079 Acps iii MalaCards C3827868 Tachycardia by ecg finding C0162532 Variegate porphyria MalaCards|HPO C0022346 Yellow skin C3272464 Ampulla of vater hepatoid adenocarcinoma UMLS C4085549 Dizziness C0305062 Tetanus toxoids HSDN C0016199 Pain flank C1708350 Hereditary leiomyomatosis and renal cell cancer UMLS C0018772 Deafness C1332140 Acrofacial dysostosis MalaCards C0020578 Hyperventilate C0039082 Syndrome HSDN C0428977 Pulse rate decrease C3280798 Cutis laxa, autosomal recessive, type ib MalaCards C0010520 Skin cyanosis C0018939 Hematological disease HSDN C0024032 Birth weight subnormal C1334229 Bowel dysplasia MalaCards C4085210 Usual severity pain C0042063 Urogenital abnormalities HSDN C1961131 Cough adverse event C0852007 Scleroderma and associated disorders OrphaNet C2024878 Cardiovascular surgery result: dyspnea C0162871 Aortic aneurysm, abdominal HSDN C0003962 Ascites C1856302 Gsd iv, nonprogressive hepatic HPO C0041657 Consciousness loss C0151699 Intracranial hemorrhages HSDN C3274924 Have been coughing C0014013 Empyema, pleural DiseaseOntology|HSDN C4085317 Diarrhea frequency C0025268 Multiple endocrine neoplasia type 2a OrphaNet C2024878 Cardiovascular surgery result: dyspnea C0812393 Cancer patients and suicide and depression HSDN C2911645 Weight loss adverse event C2984291 Glioblastoma multiforme pathway HSDN C0003862 Pain joint C1860596 Familial dyschondroplasia MalaCards C0042571 Vertigo subjective C0021783 Internal external locus of control HSDN C0026821 Cramp C0003850 Arteriosclerosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0019065 Hemorrhage intraperitoneal HSDN C0008031 Pain chest C0020456 Hyperglycemia HSDN|UMLS C0026838 Spasticity muscle C1867983 Porencephaly, familial MalaCards|HPO|UMLS C0149793 Transient monocular blindness C0003490 Aortic arch syndrome MalaCards C1557397 Adverse event associated with pain C0040582 Trachea neoplasm HSDN C0018681 Headache, cephalalgia C0030421 Paraganglioma HSDN C0042963 Symptoms vomiting C0011265 Presenile dementia HSDN C1549543 Administration method - pain C0018199 Granuloma, plasma cell HSDN C3539022 Pelvic pain decreasing in severity C1546847 Entity name part type - family HSDN C0012833 Dizzy C3151295 Hypomagnesemia 6, renal MalaCards|HPO C0013404 Respiratory difficulty C0036202 Sarcoidosis OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0393626 Opsoclonus-myoclonus syndrome HSDN C0022346 Yellow skin C0086543 Cataract nos HSDN C0028738 Nystagmus C0220701 Retinitis pigmentosa 1 MalaCards C1963237 Insomnia adverse event C0342859 Harderoporphyria HPO C2919142 Short stature adverse event C0403548 Salcedo syndrome MalaCards C0030486 Extremity paralysis, lower C0005695 Bladder neoplasm HSDN C0018775 Hearing loss bilateral C0035334 Retinitis pigmentosa HSDN C0233514 Behavior abnormal C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards C4085210 Usual severity pain C0020524 Disorders of excessive somnolence HSDN C0026858 Musculoskeletal pain C0393735 Headache disorders HSDN C2984058 Have pain C1266119 Solitary fibrous tumor HSDN C4084774 Have weight loss C0017185 Gastrointestinal neoplasms HSDN C0036572 Convulsion C2720163 Placental steroid sulfatase deficiency MalaCards C0011991 Loose stools C3276706 Small fiber neuropathy MalaCards C4085549 Dizziness C0016045 Fibroma HSDN C0008031 Pain chest C0852007 Scleroderma and associated disorders OrphaNet C2919142 Short stature adverse event C1867440 Multiple pterygium syndrome, autosomal dominant MalaCards|HPO C0007398 Catatonic C0242422 Parkinsonian disorders HSDN C0030552 Paralysis partial C1963178 Myelitis adverse event HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3827868 Tachycardia by ecg finding HSDN C0002962 Angina C0002871 Anemia HSDN C0518090 Frequency of pain question C0023646 Lichen planus HSDN C4084784 Diarrhea C0035127 Cumulative trauma disorders HSDN C0015672 Decreased energy C0012691 Dislocations HSDN C0424755 Fever symptoms C0242350 Erectile dysfunction HSDN C0042024 Urine incontinence C0037939 Spinal neoplasms HSDN C3641755 Have constipation C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0013604 Edematous C0019195 Hepatitis, viral, human HSDN C0242670 Chronic vegetative state C0004238 Atrial fibrillation HSDN C4085317 Diarrhea frequency C0264766 Rheumatic mitral stenosis HSDN C3203358 Alveolar hypoventilation C0038160 Staphylococcal infections HSDN C3829611 Nausea frequency C0013595 Eczema HSDN C0042024 Urine incontinence C2678194 Mental retardation, x-linked, syndromic, christianson type HPO C3539022 Pelvic pain decreasing in severity C2936403 46, xx disorders of sex development HSDN C2911647 Weight gain adverse event C0040411 Tongue neoplasms HSDN C4084768 Usual severity vomiting C0032827 Potassium deficiency HSDN C0020580 Decreased sensation C0014053 Encephalitis, california HSDN C4085222 Nausea C3244301 Coverage level - family HSDN C1963252 Tremor adverse event C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C4084724 Usual severity constipation C0038358 Gastric ulcer HSDN C0024031 Back pain lower back C0030319 Panic disorder HSDN C4085317 Diarrhea frequency C2963140 Arteriovenous fistula in use with two needles HSDN C4042891 Sleep wake disorders C0037421 Social isolation HSDN C0036572 Convulsion C0334579 Anaplastic astrocytoma UMLS C1963184 Nystagmus adverse event C1568249 Usher syndrome, type ii MalaCards|HPO C4084802 Usual severity diarrhea C1005359 Pica pica bird HSDN C4084775 Usual severity weight loss C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C0015970 Fever unknown origin C0003869 Arthritis, infectious HSDN C2032395 Pelvic pain on the left C0023467 Leukemia, myelocytic, acute HSDN C3641755 Have constipation C0018671 Head and neck neoplasms HSDN C1963087 Constipation adverse event C0270611 Brain damage HSDN C1963086 Confusion adverse event C1846707 Spinocerebellar ataxia 17 MalaCards|HPO C0039070 Collapse fleeting C3151463 Cpvt3 MalaCards|HPO|UMLS C3641755 Have constipation C0175694 Smith-lemli-opitz syndrome MalaCards|HPO C3641756 Have diarrhea C0206245 Amyloid neuropathies, familial MalaCards C0426579 Anorexia symptom C0346407 Pancreatic polypeptide-oma MalaCards C0000727 Abdomen acute C0007642 Cellulitis nos HSDN C0221166 Paraparesis C0027667 Cancer origin unknown HSDN C4084774 Have weight loss C0042373 Vascular diseases HSDN C0042963 Symptoms vomiting C0042870 Vitamin d deficiency HSDN C4085317 Diarrhea frequency C0004161 Athletic injuries HSDN C0024032 Birth weight subnormal C3150099 Antley-bixler syndrome with genital anomalies and disordered steroidogenesis MalaCards|HPO C0003910 Articulation disorder C0011581 Depressive disorder HSDN C2024878 Cardiovascular surgery result: dyspnea C0034186 Pyelonephritis HSDN C1549543 Administration method - pain C0020640 Inherited factor ii deficiency HSDN C0015672 Decreased energy C1264008 Chronic cold agglutinin disease MalaCards C3641756 Have diarrhea C1548777 Specimen reject reason - hemolysis HSDN C4085210 Usual severity pain C0003125 Anorexia nervosa HSDN C2024878 Cardiovascular surgery result: dyspnea C0017168 Gastroesophageal reflux disease HSDN C0018772 Deafness C0018566 Congenital hand deformities HSDN C0037384 Snore C0003873 Rheumatoid arthritis HSDN C1279888 Proteinuria of undiagnosed cause C0020517 Hypersensitivity HSDN C3146279 Coma C0029882 Otitis media HSDN C0000737 Abdomen pain C0346109 Malignant mesothelioma of peritoneum OrphaNet|UMLS|MalaCards C0728710 Pupil constriction observed C1962986 Glaucoma adverse event HSDN C1279888 Proteinuria of undiagnosed cause C0038160 Staphylococcal infections HSDN C0005745 Blepharoptosis C1842679 Thai symphalangism syndrome MalaCards C0036572 Convulsion C0162283 Nephrogenic diabetes insipidus HPO C0700078 Deep tendon reflex decrease C0270968 Limb-girdle muscular dystrophy type 2h MalaCards|HPO C1962972 Proteinuria adverse event C1963266 Uveitis adverse event HSDN C0242936 Center pain C0002950 Aneurysms inflammatory HSDN C4085642 Level of joint stiffness C2930815 Acute cerebral gaucher disease MalaCards C4084766 Vomiting C0042214 Vaccinia HSDN C0085593 Chill C0022572 Keratoacanthoma HSDN C0043094 Weight gain C0042974 Von willebrand disease HSDN C0042963 Symptoms vomiting C1963266 Uveitis adverse event HSDN C0557874 Global developmental delay C0032897 Prader-willi syndrome OrphaNet|HPO|MalaCards C4084725 Usual severity cough C1299262 Sarcoma - category (morphologic abnormality) HSDN C1963064 Anxiety adverse event C0001231 Acth syndrome, ectopic MalaCards C0013404 Respiratory difficulty C1457883 Aggressive reaction HSDN C3887638 Failure to thrive in infant C0342765 D-glyceric aciduria HPO C0728710 Pupil constriction observed C0700359 Organophosphate poisoning HSDN C4084775 Usual severity weight loss C0027022 Myeloproliferative disease HSDN C4085549 Dizziness C0011881 Diabetic nephropathy HSDN C0030193 Sense of pain C0033677 Protein-energy malnutrition HSDN C0015672 Decreased energy C0034072 Cor pulmonale HSDN C0413252 Hypothermia due to exposure C0027412 Opioid-related disorders HSDN C3641756 Have diarrhea C0035333 Retinitis HSDN C1963086 Confusion adverse event C0574109 Glycerol kinase deficiency - contiguous gene syndrome MalaCards C1963184 Nystagmus adverse event C0549307 Morning glory syndrome MalaCards|HPO C0031911 Pigment deposition C0155160 Conjunctival degeneration unsp MalaCards C0018681 Headache, cephalalgia C0542564 Cerebral hemispheric meningioma UMLS C0013604 Edematous C1009209 Tinea HSDN C0032617 High urine output C0018802 Congestive heart failure HSDN C4084773 Bothered by weight gain C0039494 Temporomandibular joint disorders HSDN C4085210 Usual severity pain C0016124 Finger injury HSDN C0030554 Abnormal sensation C0038160 Staphylococcal infections HSDN C0231341 Aging premature C0751865 Alcohol-induced disorders, nervous system HSDN C4084802 Usual severity diarrhea C0030354 Papilloma HSDN C0011570 Monopolar depression C4014588 Leukoencephalopathy, progressive, with ovarian failure MalaCards C0026884 Muteness C1366622 Mok gene HSDN C0034155 Thrombotic thrombocytopenic purpura C0009241 Cognition disorders HSDN C0151786 Weakness muscle C0030297 Pancreatic neoplasm HSDN C0009421 Comatose C0030920 Peptic ulcer HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0023860 Listeriosis DiseaseOntology|MalaCards C4084775 Usual severity weight loss C0007193 Cardiomyopathy, dilated HSDN C4084768 Usual severity vomiting C0006118 Brain neoplasms HSDN C0242936 Center pain C0027877 Neuronal ceroid-lipofuscinoses HSDN C0036572 Convulsion C0035869 Rotavirus infections HSDN C2911645 Weight loss adverse event C1561518 Pleasure - animals raised for recreation HSDN C4085548 Usual severity dizziness C0014544 Epilepsy HSDN C4085862 Bothered by nausea C0007789 Cerebral palsy HSDN C0497406 Over weight C0162425 Intent HSDN C0040822 D tremors C0038273 Stereotypic movement disorder HSDN C0151686 Growth retardation C0268496 Kramer syndrome OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0026826 High muscle tone C1999266 Depression adverse event HSDN C0424755 Fever symptoms C0022578 Keratoconus HSDN C4085210 Usual severity pain C0027022 Myeloproliferative disease HSDN C0015300 Ocular proptosis C0265211 Marshall-smith syndrome MalaCards C2911645 Weight loss adverse event C0518450 Spinal fractures HSDN C0008031 Pain chest C1263846 Attention deficit hyperactivity disorder HSDN C0023218 Lower extremity cramp C0085096 Peripheral vascular diseases UMLS C0018681 Headache, cephalalgia C0003873 Rheumatoid arthritis HSDN C0007384 Cataplexy C3179455 Niemann-pick disease, type c1 MalaCards|HPO C0034150 Skin purpura C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0009421 Comatose C0013806 Electroplexy shock therapy HSDN C0004310 Auditory disorder process C0040517 Gilles de la tourette syndrome HSDN C2364082 Hyposmia C0175704 Leopard syndrome HPO|UMLS C4084724 Usual severity constipation C0015726 Focused anxiety HSDN C2024893 Cardiovascular surgery result: fatigue C0012628 Discrete subaortic stenosis HSDN C0042510 Fibrillation paroxysmal vent C0035410 Rhabdomyolysis MalaCards C0030193 Sense of pain C0030353 Papilledema HSDN C0015970 Fever unknown origin C1636667 Disorder characterized by eosinophilia HSDN C0013404 Respiratory difficulty C0026948 Mycosis fungoides HSDN C1963086 Confusion adverse event C0024305 Lymphoma, non-hodgkin HSDN C3641753 Lacks appetite C0153014 Non-arthropod borne lymphocytic choriomeningitis DiseaseOntology|MalaCards C3463815 Feel fatigue C0042164 Uveitis HSDN C0000737 Abdomen pain C0861843 Resectable duodenal carcinoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0022364 Jaw neoplasms HSDN C0151786 Weakness muscle C4280867 Paresis as late effect of poliomyelitis UMLS C0003862 Pain joint C0010495 Cutis laxa HSDN C1856661 Cornea cloudy C0086795 Pfaundler-hurler syndrome HPO C3463815 Feel fatigue C0042131 Uterine diseases HSDN C0013404 Respiratory difficulty C0242973 Ventricular dysfunction HSDN C0019825 Voice hoarseness C0221056 Adult type dermatomyositis MalaCards C0728710 Pupil constriction observed C1418543 Phyh gene HSDN C0002170 Alopecia disorders C0268323 Familial porphyria cutanea tarda MalaCards C0040264 Ear ringing sound C1961100 Erectile dysfunction adverse event HSDN C0027497 Queasy C1854107 Hyperaldosteronism, familial, type ii MalaCards C0234230 Burn pain C0019360 Herpes zoster disease DiseaseOntology|MalaCards C4084767 Bothered by vomiting C0342792 Succinyl-coa:3-oxoacid coa transferase deficiency HPO C0426579 Anorexia symptom C0019196 Hepatitis c DiseaseOntology|HSDN|MalaCards C0042798 Vision dim C0007097 Carcinomas HSDN C3815497 Cough C0027627 Neoplasm metastasis HSDN C4084768 Usual severity vomiting C0029928 Ovarian diseases HSDN C2919142 Short stature adverse event C0587248 Costello syndrome (disorder) OrphaNet|HPO|MalaCards C0030193 Sense of pain C0684337 Ewings sarcoma-primitive neuroectodermal tumor (pnet) HSDN C1557397 Adverse event associated with pain C0017547 Gigantism HSDN C0700072 Encounter due to stillbirth C1850554 Atelosteogenesis type 2 HPO C0030193 Sense of pain C4075708 Post-infectious intercostal neuralgia UMLS C3641756 Have diarrhea C0042994 Vulvar diseases HSDN C0018784 Deafness sensorineural C1857775 Diabetes mellitus, neonatal, with congenital hypothyroidism MalaCards C0242936 Center pain C0024449 Fungal mycetoma HSDN C2237041 Shox gene with short stature C2363814 Femur-fibula-ulna complex MalaCards C0030486 Extremity paralysis, lower C0001889 Akinetic mutism HSDN C2024893 Cardiovascular surgery result: fatigue C0022336 Creutzfeldt-jakob disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003838 Arterial occlusive diseases HSDN C0026884 Muteness C0014038 Encephalitis HSDN C0024032 Birth weight subnormal C1859049 Cchs with hirschsprung disease OrphaNet|HPO|MalaCards C1963065 Apnea adverse event C0000768 Congenital abnormality HSDN C0013404 Respiratory difficulty C1527429 Increased blood npn HSDN C4084766 Vomiting C0007570 Celiac disease HSDN C0270948 Neurogenic muscular atrophy C0035372 Rett syndrome MalaCards|HPO C0178417 Anhedonia C0003125 Anorexia nervosa HSDN C0522224 Palsied C0003855 Arteriovenous fistula HSDN C0019825 Voice hoarseness C0008925 Cleft palate HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0032461 Polycythemia HSDN C4084776 Weight loss C0008073 Developmental disabilities HSDN C4084775 Usual severity weight loss C0027868 Neuromuscular diseases HSDN C4084723 Constipation C1961100 Erectile dysfunction adverse event HSDN C4084769 Vomiting frequency C1579931 Depressed - symptom HSDN C0206160 Retic count elevated C0038187 Starvation HSDN C0042571 Vertigo subjective C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0037316 Not enough sleeping C1963064 Anxiety adverse event HSDN C2984058 Have pain C0152156 Dystocia HSDN C4084784 Diarrhea C0001118 Acid base imbalance HSDN C0030193 Sense of pain C0003949 Asbestosis HSDN C0013362 Dysarthrias C0011303 Demyelinating diseases HSDN C0038002 Spleen enlargement C2931872 Free sialic acid storage disease MalaCards C4084773 Bothered by weight gain C0009475 Community mental health service HSDN C0013362 Dysarthrias C1556061 Electric injuries HSDN C2242996 Tingling C0752143 Intracranial thrombosis HSDN C1549543 Administration method - pain C0206623 Adenosquamous carcinoma HSDN C1963237 Insomnia adverse event C3888109 Acromelalgia hereditary MalaCards C1279888 Proteinuria of undiagnosed cause C0037305 Neoplasm, skull HSDN C3641756 Have diarrhea C0678202 Granulomatous enteritis MalaCards C4084767 Bothered by vomiting C0019537 High pressure nervous syndrome HSDN C1557397 Adverse event associated with pain C0043124 West nile fever HSDN C0151889 Reflexes tendon increased C1832855 Choreoathetosis/spasticity, episodic MalaCards C0086565 Liver function abnormal C3809553 Mitochondrial complex iii deficiency, nuclear type 6 MalaCards C0007398 Catatonic C1458156 Recurrent malignant neoplasm HSDN C0011991 Loose stools C0344423 Atrial flutter by ecg finding HSDN C4084725 Usual severity cough C0014850 Esophageal atresia HSDN C1963281 Vomiting adverse event C0079631 Interdisciplinary communication HSDN C0042025 Urinary incontinence stress C0038379 Eye deviation HSDN C4085549 Dizziness C0342257 Complications of diabetes mellitus HSDN C4085211 Pain distress question C0033906 Psychological theories HSDN C1557397 Adverse event associated with pain C0004239 Atrial flutter HSDN C3815497 Cough C0717360 Disease lyme vaccine HSDN C1384666 Decreased hearing C0235864 Congenital hypertrichosis lanuginosa OrphaNet|MalaCards C0033377 Caudal displacement C0265220 Pallister-hall syndrome MalaCards C0042963 Symptoms vomiting C0019285 Diaphragmatic hernia traumatic HSDN C3539893 Pelvic pain occurs with intercourse C0022665 Kidney neoplasm HSDN C0024032 Birth weight subnormal C1856796 Estren-dameshek variant of fanconi anemia HPO C0375223 Other quadriplegia C0034372 Quadriplegia UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0162627 Skin diseases, bacterial HSDN C0020578 Hyperventilate C0009946 Conversion disorder HSDN C0023380 Lethargy C0016952 Galactosemias OrphaNet|MalaCards C0349588 Stature short C1955934 Trichothiodystrophy syndromes MalaCards C0151786 Weakness muscle C0024535 Malaria, falciparum HSDN C0015469 Facial paralysis C0010035 Hereditary corneal dystrophy HSDN C0030552 Paralysis partial C0017178 Gastrointestinal diseases HSDN C0018772 Deafness C1705714 Lats1 wt allele HSDN C2203646 Jaundice C0041948 Uremia HSDN C0518090 Frequency of pain question C0242350 Erectile dysfunction HSDN C1963093 Dizziness adverse event C0004361 Autogenic therapy HSDN C0018772 Deafness C0032344 Poisoning aspects HSDN C4085549 Dizziness C0029401 Osteitis deformans HSDN C0034150 Skin purpura C0009759 Conjunctival diseases HSDN C1384666 Decreased hearing C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0018926 Emesis bloody C0334299 Carcinoid tumor no icd-o subtype HSDN C4084723 Constipation C1867969 Porphyria, acute intermittent, nonerythroid variant HPO C2015928 Outcomes otolaryngology ear pain C0349604 Intracranial meningioma MalaCards C0020672 Body temperature decreased C0206255 Malaria vaccine HSDN C4085642 Level of joint stiffness C0026706 Mucopolysaccharidosis iii OrphaNet|MalaCards C1963170 Hypothermia adverse event C0022876 Premature obstetric labor HSDN C4084725 Usual severity cough C0005779 Blood coagulation disorders HSDN C0042420 Vasovagal episode C0393911 Pure autonomic failure HSDN C2984057 Have nausea C0314657 Genetic predisposition HSDN C1963170 Hypothermia adverse event C0004943 Behcet syndrome HSDN C0018784 Deafness sensorineural C0007785 Cerebral infarction HSDN C0026821 Cramp C0752355 Myotonia fluctuans (disorder) OrphaNet|HPO C3641756 Have diarrhea C0206247 Amyloid neuropathies MalaCards C0020673 Hypothermia (central) (local) C0001118 Acid base imbalance HSDN C0033774 Skin pruritus C0032019 Pituitary neoplasms HSDN C0917816 Deficiency mental C1859564 Bardet-biedl syndrome 3 MalaCards|HPO C3463815 Feel fatigue C0410422 Chronic multifocal osteomyelitis OrphaNet|MalaCards C3274924 Have been coughing C0028433 Nose neoplasms HSDN C0007814 Cerebrospinal fluid otorrhea C0024961 Injuries maxillofacial HSDN C0040485 Wryneck C0016045 Fibroma HSDN C0007758 Cerebellar ataxia C1704421 Skin pigmentation disorder HSDN C4020887 Photodysphoria C2752147 Xeroderma pigmentosum, complementation group c HPO C4084724 Usual severity constipation C0011265 Presenile dementia HSDN C2911647 Weight gain adverse event C0034089 Pulmonary valve stenosis HSDN C0031911 Pigment deposition C0349623 Primary melanocytic lesion of meninges MalaCards C4084784 Diarrhea C0034929 Reflex HSDN C2911647 Weight gain adverse event C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C2919142 Short stature adverse event C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0037763 Spasm C0264404 Allergic bronchitis chronic UMLS C0030554 Abnormal sensation C0036974 Shock HSDN C0497406 Over weight C0018790 Cardiac arrest HSDN C0233767 Hallucinations tactile C0018524 Hallucinations UMLS C0018784 Deafness sensorineural C0034065 Pulmonary embolism HSDN C0018784 Deafness sensorineural C0018671 Head and neck neoplasms HSDN C0917816 Deficiency mental C2936904 Opitz gbbb syndrome, x-linked OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C0024215 Lymphangiectasis, intestinal MalaCards C0231528 Muscle pain generalized C0272295 Purpura, rheumatica MalaCards C4084776 Weight loss C1835664 Tylosis with esophageal cancer MalaCards C1963091 Diarrhea adverse event C0014175 Endometriosis HSDN C0015672 Decreased energy C0001173 Adult pyloric stenosis HSDN C0518090 Frequency of pain question C0033906 Psychological theories HSDN C3898969 Have been vomiting C0039128 Syphilis HSDN C0349588 Stature short C1842763 Spondyloenchondrodysplasia with immune dysregulation MalaCards|HPO C0085650 Purpura fulminans C0752308 Hypoxia-ischemia, brain HSDN C2237041 Shox gene with short stature C3549874 Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly MalaCards C4085661 Usual severity nausea C0002395 Alzheimer's disease HSDN C0015230 Exanthem C0878675 Erdheim-chester disease MalaCards C0024031 Back pain lower back C0011854 Diabetes mellitus, insulin-dependent HSDN C1557397 Adverse event associated with pain C0206231 Bone malalignment HSDN C4084775 Usual severity weight loss C1000587 Pemphigus HSDN C1961100 Erectile dysfunction adverse event C0268386 Amyloid polyneuropathy, swiss type MalaCards C0037036 Increased salivation C1859711 Arthrogryposis multiplex congenita with whistling face MalaCards C0034155 Thrombotic thrombocytopenic purpura C1546847 Entity name part type - family HSDN C0036572 Convulsion C0040425 Tonsillitis HSDN C0009806 Constipate C0000771 Abnormalities, drug induced HSDN C0030193 Sense of pain C0029944 Drug overdose HSDN C0003126 Smell loss C2675302 Kallmann syndrome 5 MalaCards|HPO C1557397 Adverse event associated with pain C1258666 Myxoid cyst HSDN C0232847 Enuresis primary C3472580 Intermittent urinary incontinence UMLS C0022346 Yellow skin C0006663 Calcinosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0162871 Aortic aneurysm, abdominal HSDN C0027497 Queasy C0034929 Reflex HSDN C1549543 Administration method - pain C0009663 Condylomata acuminata HSDN C0002963 Angina variant C2984299 Asthma pathway HSDN C0016382 Cutaneous vascular engorgement C0021100 Bullous impetigo OrphaNet|MalaCards C2984058 Have pain C0019045 Hemoglobinopathies HSDN C0033377 Caudal displacement C0013261 Duane retraction syndrome MalaCards|HPO C0018772 Deafness C0001193 Apert syndrome MalaCards|HSDN|HPO C1963180 Neck pain adverse event C0033578 Prostatic neoplasms HSDN C1963091 Diarrhea adverse event C0002986 Fabry disease MalaCards|HPO C4084766 Vomiting C0007820 Cerebrovascular disorders HSDN C0349489 Fetal hypoxia C0085207 Gestational diabetes HSDN C4084769 Vomiting frequency C0344479 Spinal cord myelodysplasia HSDN C0557874 Global developmental delay C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0023012 Delay language C1848211 Mental retardation with psychosis, pyramidal signs, and macroorchidism MalaCards|HPO C3829611 Nausea frequency C0348018 Projections HSDN C0013604 Edematous C1690964 Cataract HSDN C2984058 Have pain C0025309 Meningoencephalitis HSDN C3163620 Hypotension adverse event C1449842 Pseudohypoaldosteronism, type i, autosomal dominant HPO C0033774 Skin pruritus C0017168 Gastroesophageal reflux disease HSDN C0221166 Paraparesis C0007784 Cerebral hemisphere hemorrhage HSDN C0042024 Urine incontinence C0038663 Suicide attempt HSDN C2203646 Jaundice C0038379 Eye deviation HSDN C4085317 Diarrhea frequency C0014848 Esophageal achalasia HSDN C0522224 Palsied C0019195 Hepatitis, viral, human HSDN C0851578 Disorder sleep C0036690 Septicemia HSDN C4084773 Bothered by weight gain C0850803 Anaphylaxis (non medication) HSDN C4084768 Usual severity vomiting C0024236 Lymphedema HSDN C4085317 Diarrhea frequency C0344311 Blister HSDN C0018681 Headache, cephalalgia C1833163 Enamel hypoplasia, cataracts, and aqueductal stenosis UMLS C2024878 Cardiovascular surgery result: dyspnea C0002994 Angioedema HSDN C0037317 Sleep disturbance C0008312 Primary biliary cirrhosis MalaCards C0013604 Edematous C2316212 Cryopyrin-associated periodic syndromes MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1579931 Depressed - symptom HSDN C1963093 Dizziness adverse event C0021361 Female infertility HSDN C4085211 Pain distress question C0206663 Neuroectodermal tumor, primitive HSDN C0015672 Decreased energy C0162871 Aortic aneurysm, abdominal HSDN C0036572 Convulsion C0268623 Tyrosinemia, type iii MalaCards|HPO|UMLS C2911647 Weight gain adverse event C0002880 Autoimmune hemolytic anemia HSDN C0424755 Fever symptoms C0836924 Thrombocytosis HSDN C4084727 Cough frequency C0525045 Mood disorders HSDN C0043094 Weight gain C3814778 Hemolytic index HSDN C0013362 Dysarthrias C0042875 Vitamin e deficiency HSDN C0271215 Blindness legal C1318020 Stromal keratitis MalaCards C1549543 Administration method - pain C0042376 Vascular headaches HSDN C0019079 Bloody sputum C0010074 Coronary vessel anomalies HSDN C0576456 Poor feeding C0795889 Allan-herndon-dudley syndrome (ahds) MalaCards C0019214 Hepatosplenomegaly C2931838 Familial hdl deficiency MalaCards C0013404 Respiratory difficulty C0751552 Malignant neoplasm of thymus MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0004623 Bacterial infections HSDN C3146279 Coma C0007134 Renal cell carcinoma HSDN C0041105 Jaw spasm C0406810 Carney complex MalaCards C3539889 Pelvic pain increasing in severity C0206687 Carcinoma, endometrioid HSDN C0917967 Pupil function anomaly C0376329 New variant creutzfeldt-jakob disease MalaCards C1963091 Diarrhea adverse event C3668816 Inflammation of non-human mammary gland HSDN C0007166 Cardiac output decreased C0036202 Sarcoidosis HSDN C0812426 Kidney problem C0041948 Uremia UMLS C0271215 Blindness legal C0265313 Weill-marchesani syndrome HPO C4084802 Usual severity diarrhea C0029001 Onchocerciasis HSDN C0038002 Spleen enlargement C0543697 Mixed cryoglobulinemia OrphaNet|MalaCards C4084724 Usual severity constipation C2609414 Acute kidney injury HSDN C0001825 Agraphia C0033367 Projective techniques HSDN C0000737 Abdomen pain C1963106 Esophagitis adverse event HSDN C0020673 Hypothermia (central) (local) C0031117 Peripheral neuropathy HSDN C0019209 Large liver C0342280 Aredyld OrphaNet|MalaCards C3539895 Pelvic pain occurs with bowel movement C0206630 Endometrial stromal sarcoma HSDN C0030193 Sense of pain C0035008 Reinforcement schedules HSDN C4085211 Pain distress question C0007124 Noninfiltrating intraductal carcinoma HSDN C0151786 Weakness muscle C4082299 Bulbar palsy UMLS C0004604 Pain back C0349604 Intracranial meningioma MalaCards C0004604 Pain back C0023470 Myeloid leukemia HSDN C0751265 Learning disability C0221060 Mobius syndrome MalaCards C4085222 Nausea C0033871 Psychiatric status rating scales HSDN C0405584 Intolerance; sucrose C0699848 Disaccharidase deficiency UMLS C4084773 Bothered by weight gain C0037274 Dermatologic disorders HSDN C0028738 Nystagmus C2745996 Fitzsimmons syndrome MalaCards C4085210 Usual severity pain C0037280 Skin diseases, parasitic HSDN C0851578 Disorder sleep C0017636 Glioblastoma HSDN C2032396 Pelvic pain on the right C0007527 Cecal disease HSDN C0085636 Light sensitivity C3665342 Progressive cone dystrophy MalaCards C0030486 Extremity paralysis, lower C4084909 Depression subordinate domain HSDN C3829611 Nausea frequency C3887662 Intraspinal neoplasm HSDN C4084776 Weight loss C0016510 Foot diseases HSDN C0020649 Blood pressure decreased C1846344 Bartter syndrome, type 3, with hypocalciuria HPO C3541349 Syncope C0085615 Right bundle branch block MalaCards C0032227 Effusion pleural C0340834 Hennekam lymphangiectasia lymphedema syndrome HPO C0575081 Abnormal gait C0221061 Behr syndrome MalaCards|HPO C3463815 Feel fatigue C1457883 Aggressive reaction HSDN C0242936 Center pain C0021295 Infant, premature, diseases HSDN C3829611 Nausea frequency C0032269 Pneumococcal infections HSDN C0034933 Abnormal reflexes C0027051 Myocardial infarction HSDN C1069915 Vertigo C0242287 Isaacs syndrome HPO C4085317 Diarrhea frequency C3714602 Staphylococcal toxic shock syndrome MalaCards C1963252 Tremor adverse event C0020473 Hyperlipidemia HSDN C0423714 Genitofemoral nerve neuralgia C0031121 Neuralgia peripheral UMLS C1963184 Nystagmus adverse event C2930979 Acrofacial dysostosis richieri costa guion-almeida type MalaCards C0036572 Convulsion C0041956 Ureteral obstruction HSDN C2911645 Weight loss adverse event C0003486 Aortic aneurysm HSDN C0413252 Hypothermia due to exposure C0023055 Laryngeal neoplasm HSDN C2700617 Irritation - emotion C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0557874 Global developmental delay C1846265 Microphthalmia, syndromic 2 MalaCards|HPO C4084788 Have dizziness C0079731 B-cell lymphomas HSDN C0344307 Analgesia C3808991 Congenital disorder of deglycosylation MalaCards C0023015 Language handicap C0037415 Social facilitation HSDN C1963184 Nystagmus adverse event C0546878 Salaam spasms MalaCards C0000727 Abdomen acute C0270611 Brain damage HSDN C4042891 Sleep wake disorders C0041228 African trypanosomiasis HSDN C0010520 Skin cyanosis C1562503 Vein of galen malformations HSDN C0349588 Stature short C4015261 Polyendocrine-polyneuropathy syndrome MalaCards C0006370 Bulimia C0349231 Phobic anxiety disorder HSDN C4085222 Nausea C0007787 Transient ischemic attack HSDN C4084802 Usual severity diarrhea C3665623 Serum albumin level decreased below normal HSDN C0015468 Face pain C0005695 Bladder neoplasm HSDN C0026826 High muscle tone C0008073 Developmental disabilities HSDN C3641756 Have diarrhea C0751651 Mitochondrial diseases HSDN C1963281 Vomiting adverse event C3714509 Nutrition disorders HSDN C1963281 Vomiting adverse event C0031090 Periodontal diseases HSDN C0232466 Feeding difficulty C2931296 Yorifuji okuno syndrome OrphaNet|HPO C0085650 Purpura fulminans C0026272 Mixed connective tissue disease HSDN C0009676 Confusion state C0027849 Neuroleptic malignant syndrome HSDN C0086437 Joint hypermobility C0265326 Bannayan-riley-ruvalcaba syndrome MalaCards|HPO C0727671 Red cross toothache drops C0040436 Dental erosion HSDN C0026826 High muscle tone C0007001 Carbohydrate metabolism, inborn errors HSDN C0018784 Deafness sensorineural C0018188 Granuloma HSDN C0036572 Convulsion C4040796 Status epilepticus due to intractable idiopathic generalised epilepsy UMLS C4084774 Have weight loss C1385938 Acanthocephaliasis MalaCards C0028961 Urine output decreased C0031190 Persistent fetal circulation syndrome HSDN C0043352 Absent salivary secretion C2939462 Immunoglobulin deposition disease MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024788 Green monkey virus disease DiseaseOntology|MalaCards C4085661 Usual severity nausea C0162871 Aortic aneurysm, abdominal HSDN C4085211 Pain distress question C0025309 Meningoencephalitis HSDN C1963091 Diarrhea adverse event C0031345 Pharyngeal diseases HSDN C3539023 Pelvic pain increasing in frequency C0314657 Genetic predisposition HSDN C0032227 Effusion pleural C0878675 Erdheim-chester disease MalaCards C4084775 Usual severity weight loss C0751955 Brain infarction HSDN C0003862 Pain joint C1850155 Torg-winchester syndrome MalaCards|HPO C0000737 Abdomen pain C0015745 Ingestive behavior HSDN C0085602 Polydypsia C0031039 Effusion pericardial HSDN C0413252 Hypothermia due to exposure C0014457 Eosinophilia HSDN C4085211 Pain distress question C0403447 Chronic kidney insufficiency HSDN C0241210 Speaking delay C1859568 Bardet-biedl syndrome 10 HPO C0042963 Symptoms vomiting C0233629 Thinking and speaking disturbances HSDN C0557874 Global developmental delay C2931638 Chromosome 8, monosomy 8p23 1 MalaCards C4085211 Pain distress question C0027868 Neuromuscular diseases HSDN C0024031 Back pain lower back C1704275 Pyomyositis HSDN C4050613 Anxiety C1832884 Hemiplegic migraine, familial type 1 MalaCards|HPO C4084766 Vomiting C0040809 Patient refusal of treatment HSDN C0020438 Hypercalciuria C0020501 Primary hyperoxaluria HSDN C0015799 Feminisation C0333693 Triploidy syndrome HSDN C1069915 Vertigo C0020443 Hypercholesterolemia HSDN C0036572 Convulsion C3280730 Epilepsy, familial temporal lobe, 5 MalaCards C0043094 Weight gain C0206255 Malaria vaccine HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1861964 Callosities, hereditary painful OrphaNet|MalaCards C4084774 Have weight loss C0018021 Goiter HSDN C0150055 Pain chronic C0015802 Femur fracture HSDN C4084802 Usual severity diarrhea C1848590 Vascular hyalinosis MalaCards C0850758 Pain pelvic C0038941 Incisional infection HSDN C0242936 Center pain C1656583 Rosacea HSDN C0040485 Wryneck C0022410 Joint instability HSDN C0025287 Meningitis-like C0023418 Leukemia HSDN C0013421 Dystonia C0005491 Biofeedback HSDN C0151786 Weakness muscle C0265224 Freeman-sheldon syndrome MalaCards|HPO C1549543 Administration method - pain C0031142 Peritoneal diseases HSDN C3898969 Have been vomiting C1253937 Pericardial effusion HSDN C0851578 Disorder sleep C0041234 Chagas disease HSDN C0522224 Palsied C2028283 History of premature birth HSDN C4085549 Dizziness C0009375 Colonic neoplasms HSDN C4084727 Cough frequency C0015397 Disorder of eye HSDN C1069915 Vertigo C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C4085211 Pain distress question C0001420 Papillary adenocarcinoma HSDN C0151786 Weakness muscle C0151744 Myocardial ischemia HSDN C4085862 Bothered by nausea C0038159 Food poisoning, staphylococcal DiseaseOntology|MalaCards C1549543 Administration method - pain C0206620 Lymphangioma, cystic HSDN C2984058 Have pain C0311468 Increased bilirubin level (finding) HSDN C0036572 Convulsion C1848392 Zunich neuroectodermal syndrome HPO|UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0014038 Encephalitis HSDN C0022346 Yellow skin C0861856 Bile duct colloid carcinoma UMLS C4085210 Usual severity pain C0019337 Heroin dependence HSDN C1962972 Proteinuria adverse event C0038160 Staphylococcal infections HSDN C0000727 Abdomen acute C0812393 Cancer patients and suicide and depression HSDN C0015300 Ocular proptosis C0265301 Sclerosteosis HPO C0042963 Symptoms vomiting C0919267 Ovarian neoplasm HSDN C0002963 Angina variant C1458155 Mammary neoplasms HSDN C1145670 Failure respiratory C0175709 Centronuclear myopathy OrphaNet C0270327 Bed wetting C2748572 Sesame syndrome HPO C0917816 Deficiency mental C0432443 Deletion of long arm of chromosome 18 OrphaNet|MalaCards C1961131 Cough adverse event C0020541 Hypertension, portal HSDN C4084776 Weight loss C0034628 Radius fracture HSDN C0518090 Frequency of pain question C0017086 Gangrene HSDN C0003550 Broca aphasia C0006105 Brain abscess HSDN C4084774 Have weight loss C1866552 Paragangliomas 2 (disorder) MalaCards C4085317 Diarrhea frequency C0282687 Hemorrhagic fever, ebola DiseaseOntology|OrphaNet|MalaCards C0030552 Paralysis partial C1857395 De toni-debre-fanconi syndrome HSDN C0234523 Apraxia, classic C0751955 Brain infarction HSDN C0392699 Dysaesthesia C0206734 Hemangioblastoma MalaCards C2984057 Have nausea C0270611 Brain damage HSDN C0012833 Dizzy C0155507 Labyrinthitis toxic UMLS C0036572 Convulsion C1704436 Peripheral arterial diseases HSDN C2242996 Tingling C0006035 Borrelia infections MalaCards C4085862 Bothered by nausea C1962958 Hematoma adverse event HSDN C0162298 Stiffness joints C2931051 Camptodactyly, joint contractures, facial skeletal defects OrphaNet|MalaCards C1860844 Sparse, thin hair C0432235 Cranioectodermal dysplasia OrphaNet|HPO|MalaCards C0000737 Abdomen pain C3899977 Bclc stage c hepatocellular carcinoma UMLS C0043094 Weight gain C0860549 Refeed syndrome HSDN C1963170 Hypothermia adverse event C0011119 Decompression sickness HSDN C4084773 Bothered by weight gain C0036421 Systemic scleroderma HSDN C0015469 Facial paralysis C0033817 Pseudomonas infections HSDN C4084784 Diarrhea C0034069 Pulmonary fibrosis HSDN C3898969 Have been vomiting C0018824 Heart valve disease HSDN C3887784 Decreased urine output C0013336 Dwarfism HSDN C0011991 Loose stools C0002726 Amyloidosis HSDN C0001707 Aerophagia C0520679 Sleep apnea, obstructive HSDN C1838869 Proximal neurogenic muscle weakness C1866785 Spheroid body myopathy MalaCards|HPO C3641755 Have constipation C0042812 Acuity visual HSDN C4085210 Usual severity pain C0035459 Atrophic rhinitis HSDN C0003113 Anomia C0036356 Schizophrenics--language HSDN C0036572 Convulsion C1860707 Tuberous sclerosis 2 (disorder) UMLS C2242996 Tingling C2984289 Melanoma pathway HSDN C2203646 Jaundice C0001624 Adrenal gland neoplasms HSDN C0036572 Convulsion C0017075 Ganglioneuroma UMLS C4085210 Usual severity pain C1548483 Leishmaniasis vaccine HSDN C4084768 Usual severity vomiting C2076600 Influenza due to influenza a virus subtype h1n1 MalaCards C0011991 Loose stools C0003492 Aortic coarctation HSDN C4084769 Vomiting frequency C0027121 Myositis HSDN C1384666 Decreased hearing C0334123 Histiocytosis, lipoid MalaCards C0039070 Collapse fleeting C0949658 Cardiomyopathy, hypertrophic, familial HSDN C0035078 Failure kidney C1868148 Potter type iii polycystic kidney disease HPO C0700078 Deep tendon reflex decrease C0751544 Tangier disease neuropathy MalaCards C0023885 Liver abscess C0345904 Malignant neoplasm of liver MalaCards C0041667 Low weight C3554002 Pbd12a MalaCards C1963093 Dizziness adverse event C0009324 Ulcerative colitis HSDN C0917816 Deficiency mental C2316212 Cryopyrin-associated periodic syndromes MalaCards C0042963 Symptoms vomiting C0007820 Cerebrovascular disorders HSDN C3539020 Pelvic pain decreasing in frequency C0020550 Hyperthyroidism HSDN C0018784 Deafness sensorineural C1865143 Branchiootic syndrome 1 MalaCards C4084773 Bothered by weight gain C0852795 Increased insulin level HSDN C0019572 Hairiness C1306214 Acth-secreting pituitary adenoma HPO C0015672 Decreased energy C2937287 Hematolysis HSDN C0221752 Rbc urine C2931254 Alport syndrome, recessive type MalaCards C1963065 Apnea adverse event C0752294 Sleep arousal disorders HSDN C0018681 Headache, cephalalgia C1333630 Foramen magnum meningioma UMLS C0010520 Skin cyanosis C0810021 Other lower respiratory disease UMLS C2096293 Ent surgical result ear vertigo C0001430 Adenoma HSDN C2315100 Pediatric failure to thrive C0860239 Catheter infections related HSDN C0040485 Wryneck C0158298 Other and unspecified back disorders UMLS C0426579 Anorexia symptom C0034494 Rabies (disorder) OrphaNet|MalaCards C0013604 Edematous C1456781 Benign melanocytic nevus HSDN C4084776 Weight loss C2936797 Acid cholesteryl ester hydrolase deficiency, type 2 OrphaNet C0030975 Disorders perception C0020701 Somatization disorder HSDN C4084784 Diarrhea C0018889 Helminthiasis HSDN C0270327 Bed wetting C1846980 Senior-loken syndrome 3 MalaCards C2024878 Cardiovascular surgery result: dyspnea C0030286 Pancreatic diseases HSDN C0030193 Sense of pain C0206638 Giant cell tumor of bone UMLS C0013421 Dystonia C0019202 Hepatolenticular degeneration MalaCards|HPO C0003550 Broca aphasia C0020936 Imitative behaviors HSDN C0030193 Sense of pain C1334642 Maxillary sinus adenocarcinoma UMLS C1963281 Vomiting adverse event C0018571 Hand injury HSDN C3887638 Failure to thrive in infant C3809039 Mental retardation, autosomal recessive 36 MalaCards C0002965 Crescendo angina C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0751495 Seizure focal C1969810 Febrile convulsions, familial, 8 HPO C0151315 Neck rigid C4225273 Spondyloepiphyseal dysplasia, stanescu type UMLS C0022408 Disorder joint C0038015 Spondyloepiphyseal dysplasia MalaCards C0040822 D tremors C0017638 Glioma HSDN C0042963 Symptoms vomiting C0022821 Kyphosis deformity of spine HSDN C0019825 Voice hoarseness C0161410 Accessory nerve injuries HSDN C1963252 Tremor adverse event C1963064 Anxiety adverse event HSDN C0013604 Edematous C0282606 Myomatous neoplasm HSDN C2237041 Shox gene with short stature C2675860 Diamond-blackfan anemia 4 MalaCards C2911645 Weight loss adverse event C0004442 Avoidance learning HSDN C0011991 Loose stools C0005417 Bile duct fistula HSDN C2203646 Jaundice C2911643 Encounter due to family history of osteoporosis HSDN C0027066 Myoclonic jerking C0919267 Ovarian neoplasm HSDN C0024031 Back pain lower back C0016045 Fibroma HSDN C0004604 Pain back C3495422 Finding relating to sexuality and sexual activity HSDN C0042964 Anticipatory vomiting C0027947 Neutropenia HSDN C2919142 Short stature adverse event C1832444 Ectodermal dysplasia with natal teeth, turnpenny type MalaCards C2911645 Weight loss adverse event C0025517 Metabolic diseases HSDN C0000737 Abdomen pain C0023241 Legionnaires' disease MalaCards C0022638 Ketosis C3809553 Mitochondrial complex iii deficiency, nuclear type 6 MalaCards C0020458 Hyperhydrosis C0004576 Babesiosis OrphaNet|MalaCards C0013404 Respiratory difficulty C2931642 Benign symmetrical lipomatosis HSDN C0009806 Constipate C0079294 Epidermolysis bullosa dystrophica OrphaNet C0241210 Speaking delay C0795830 Chromosome 9p deletion syndrome MalaCards C4084769 Vomiting frequency C1835888 Diarrhea 4, malabsorptive, congenital MalaCards|HPO C0020639 Hypoproteinaemia C0403399 Finnish congenital nephrotic syndrome MalaCards|HPO C0035078 Failure kidney C3537440 Cystinosis, infantile nephropathic MalaCards C1963184 Nystagmus adverse event C0035334 Retinitis pigmentosa OrphaNet|HPO|MalaCards C0016382 Cutaneous vascular engorgement C0014132 Endocrine gland neoplasms HSDN C4084723 Constipation C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C0041657 Consciousness loss C1962976 Ventricular fibrillation adverse event HSDN C0023530 Leukopenia C1836861 Fanconi anemia, complementation group i MalaCards C0041105 Jaw spasm C0011570 Mental depression HSDN C4042891 Sleep wake disorders C0024299 Lymphoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1302808 Myopericytoma HSDN C3641755 Have constipation C2673612 Epidermolysis bullosa dystrophica inversa, autosomal recessive HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0028850 Ocular motility disorders HSDN C3641756 Have diarrhea C0272129 Donath-landsteiner hemolytic anemia MalaCards C0085606 Urination urgency C1846046 Spastic paraplegia 16, x-linked (disorder) MalaCards C0010038 Corneal opacity disorder C0015393 Eye abnormalities MalaCards C0399591 Sublingual sialectasia C0459149 Disorder of soft tissue of head UMLS C0012569 Double vision C0007762 Cerebellar neoplasms HSDN C2315100 Pediatric failure to thrive C1861922 Campomelic dysplasia MalaCards|HPO C4085211 Pain distress question C0022364 Jaw neoplasms HSDN C0010200 Cough symptom C0748164 Pulmonary nodule multiple HSDN C1963281 Vomiting adverse event C0027149 Myxoma HSDN C4085317 Diarrhea frequency C0024236 Lymphedema HSDN C0015469 Facial paralysis C0027126 Myotonic dystrophy MalaCards C0013390 Cramps menstrual C0269995 Galactorrhea associated with childbirth HSDN C0013604 Edematous C0206062 Lung diseases, interstitial HSDN C1260922 Respiratory abnormality C2937225 Biotin deficiency disease MalaCards C0020672 Body temperature decreased C0151744 Myocardial ischemia HSDN C0162298 Stiffness joints C1869115 Weill-marchesani syndrome, autosomal dominant HPO|UMLS C1384666 Decreased hearing C0796068 Oculodigitoesophagoduodenal syndrome HPO C0030193 Sense of pain C0027070 Myoepithelioma HSDN C0011991 Loose stools C2931876 Hirschsprung disease 1 MalaCards C0151786 Weakness muscle C0042769 Virus diseases HSDN C0020580 Decreased sensation C0013010 Cerebral lateralization HSDN C1963090 Dehydration adverse event C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards C1962957 Flushing adverse event C0026865 Mushroom poisoning HSDN C2919142 Short stature adverse event C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C0344423 Atrial flutter by ecg finding HSDN C4084767 Bothered by vomiting C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0038868 Supranuclear palsy progressive C0600104 Obsessive compulsive behavior HSDN C3641756 Have diarrhea C0597109 Nurse's role HSDN C4084723 Constipation C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3887638 Failure to thrive in infant C0043251 Wounds and injuries HSDN C0018772 Deafness C0009324 Ulcerative colitis HSDN C0013362 Dysarthrias C1848533 Ataxia with vitamin e deficiency OrphaNet|HPO C0013362 Dysarthrias C0017922 Glycogen storage disease type iii HSDN C1963090 Dehydration adverse event C1846344 Bartter syndrome, type 3, with hypocalciuria HPO C0424755 Fever symptoms C0152936 Plague, septicemic DiseaseOntology|MalaCards C4084774 Have weight loss C0028768 Obsessive-compulsive disorder HSDN C0004604 Pain back C0027059 Myocarditis HSDN C4049644 Depression C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C0237326 Defecation pain C1836929 Emanuel syndrome OrphaNet|MalaCards C3146279 Coma C0027149 Myxoma HSDN C0013362 Dysarthrias C0023264 Leigh disease MalaCards|HPO C0344315 Mood depressed C2930674 Babesioses, human MalaCards C0000727 Abdomen acute C0036974 Shock HSDN C4084726 Distress cough C0042029 Urinary tract infection HSDN C0043094 Weight gain C0011265 Presenile dementia HSDN C0149793 Transient monocular blindness C0524802 Nerve optic tumor HSDN C1963137 Hydrocephalus adverse event C2930798 Alexanders leukodystrophy MalaCards C1860844 Sparse, thin hair C1849401 Retinitis pigmentosa, deafness, mental retardation, and hypogonadism MalaCards C4085211 Pain distress question C0020437 Hypercalcemia HSDN C0494475 Seizure generalized tonic clonic C1849508 Epilepsy, pyridoxine-dependent MalaCards|HPO C0349588 Stature short C1865644 Plantar lipomatosis, unusual facies, and developmental delay MalaCards|HPO C0518090 Frequency of pain question C0018128 Graft occlusion, vascular HSDN C1963249 Tinnitus adverse event C4049644 Depression HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0036202 Sarcoidosis HSDN C3274924 Have been coughing C0013291 Duodenal neoplasms HSDN C0018772 Deafness C4050613 Anxiety scale (basc-2) HSDN C0037316 Not enough sleeping C0270611 Brain damage HSDN C1962956 Flatulence adverse event C0038357 Rupture stomach HSDN C0013604 Edematous C0221757 Alpha 1-antitrypsin deficiency HSDN C1963086 Confusion adverse event C1000483 Genus anemia HSDN C2203646 Jaundice C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards C0027498 Nausea vomiting C0279628 Adenocarcinoma of esophagus OrphaNet C3887638 Failure to thrive in infant C0268574 Hyperleucine-isoleucinemia MalaCards C0221166 Paraparesis C0751072 Frontotemporal lobar degeneration MalaCards C0700078 Deep tendon reflex decrease C3279722 Myopathy, distal, 4 MalaCards C4084767 Bothered by vomiting C0151740 Intracranial hypertension HSDN C0018772 Deafness C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C3887873 Hearing loss C0030567 Parkinson disease HSDN C3887638 Failure to thrive in infant C0042580 Vesico-ureteral reflux HSDN C1963252 Tremor adverse event C0037928 Spinal cord diseases HSDN C0009421 Comatose C0026528 Moral code HSDN C0018772 Deafness C1456784 Paranoia HSDN C1557397 Adverse event associated with pain C0037072 Diseases sigmoid HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0020480 Hyperlipoproteinemia type iv HSDN C4084727 Cough frequency C0037933 Spinal diseases HSDN C2315100 Pediatric failure to thrive C1833104 Diabetes mellitus, permanent neonatal OrphaNet|HPO|MalaCards C0022346 Yellow skin C3900102 Adult fibrolamellar carcinoma UMLS C4085862 Bothered by nausea C1527336 Sjogren's syndrome HSDN C2237041 Shox gene with short stature C2931889 Oral-facial-digital syndrome, type 2 MalaCards C0086565 Liver function abnormal C3809339 Combined oxidative phosphorylation deficiency 16 MalaCards C3539892 Pelvic pain in front C0033578 Prostatic neoplasms HSDN C2919142 Short stature adverse event C1866168 Acrofacial dysostosis, palagonia type MalaCards C2029884 Hearing loss by exam C0005591 Avian disease HSDN C3641756 Have diarrhea C1553188 Hemolysis - observation HSDN C1963281 Vomiting adverse event C1963229 Retinal detachment adverse event HSDN C0040822 D tremors C0270589 Porcine stress syndrome UMLS C4084788 Have dizziness C0460137 Push down or depress HSDN C3898969 Have been vomiting C0016169 Pathologic fistula HSDN C1963071 Back pain adverse event C1963266 Uveitis adverse event HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0206629 Pulmonary blastoma OrphaNet|HSDN|MalaCards C4084723 Constipation C0238015 Autonomic dysreflexia HSDN C0152447 Urethra discharge C0232977 Leaking semen UMLS C0010038 Corneal opacity disorder C0796092 Oculo-cerebro-cutaneous syndrome MalaCards C0000737 Abdomen pain C0001529 Dercum disease HSDN C0031911 Pigment deposition C0206687 Carcinoma, endometrioid MalaCards C0007859 Pain neck C0019621 Histiocytosis, langerhans-cell HSDN C0018772 Deafness C1579931 Depressed - symptom HSDN C0002622 Amnesias C0011849 Diabetes mellitus HSDN C0085650 Purpura fulminans C0517555 Venous thrombosis after immobility HSDN C0018772 Deafness C0017152 Gastritis HSDN C0557874 Global developmental delay C0021171 Bloch sulzberger syndrome MalaCards|HPO C0018681 Headache, cephalalgia C0333596 Deposition of iron HSDN C3463815 Feel fatigue C0002736 Amyotrophic lateral sclerosis OrphaNet|HPO|MalaCards C3163620 Hypotension adverse event C0852654 21-hydroxylase deficiency MalaCards C1963087 Constipation adverse event C2750784 Spastic paraplegia 44, autosomal recessive (disorder) MalaCards|HPO C0013604 Edematous C0333497 Segmental glomerulosclerosis HPO C1557397 Adverse event associated with pain C0234421 Conscious HSDN C2096293 Ent surgical result ear vertigo C0752322 Epilepsy, partial, sensory HSDN C3463815 Feel fatigue C0027746 Nerve degeneration HSDN C0413252 Hypothermia due to exposure C0011882 Diabetic neuropathies HSDN C1263846 Attention deficit disorder with hyperactivity C0265498 48, xxxy syndrome OrphaNet|MalaCards C0012833 Dizzy C0020502 Hyperparathyroidism HSDN C0150055 Pain chronic C0005967 Bone neoplasms HSDN C0011991 Loose stools C0034494 Rabies (disorder) OrphaNet|HSDN|MalaCards C0002962 Angina C0003469 Anxiety disorders HSDN C0013395 Indigestion C0013291 Duodenal neoplasms HSDN C0021359 Infertility C1867859 Prader-willi-like syndrome associated with chromosome 6 HPO C0242936 Center pain C0030920 Peptic ulcer HSDN C0231807 Dyspnea exertional C0036202 Sarcoidosis UMLS C1549543 Administration method - pain C0028064 Niemann-pick diseases HSDN C0151686 Growth retardation C2749560 Methemoglobinemia, type ii HPO C2024878 Cardiovascular surgery result: dyspnea C0023448 Lymphoid leukemia HSDN C0917816 Deficiency mental C0796162 Sonoda syndrome MalaCards C2984057 Have nausea C0020179 Huntington disease HSDN C0004093 Asthenia C0026650 Movement disorders HSDN C0009676 Confusion state C0020538 Hypertensive disease HSDN C0013456 Pain ear C0001163 Vestibulocochlear nerve diseases HSDN C0030193 Sense of pain C0042109 Urticaria HSDN C0022408 Disorder joint C1861580 Chondrocalcinosis due to apatite crystal deposition MalaCards C1963071 Back pain adverse event C0004153 Atherosclerosis HSDN C4084775 Usual severity weight loss C0040038 Thromboembolism HSDN C3539020 Pelvic pain decreasing in frequency C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0019214 Hepatosplenomegaly C0685894 Congenital absence of thymus MalaCards C0026821 Cramp C0021390 Inflammatory bowel diseases HSDN C0022346 Yellow skin C0038661 Suicide HSDN C0011991 Loose stools C0021843 Intestinal obstruction HSDN C4084766 Vomiting C0020428 Hyperaldosteronism HSDN C0002965 Crescendo angina C0027726 Nephrotic syndrome HSDN C0162834 Hyperpigmentation C1276127 Sporadic porphyria cutanea tarda MalaCards C0042963 Symptoms vomiting C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO|UMLS C0424755 Fever symptoms C0026143 Milker's nodules DiseaseOntology|MalaCards C4084766 Vomiting C1253937 Pericardial effusion HSDN C0040485 Wryneck C3887667 Retrocollis UMLS C4042891 Sleep wake disorders C0035436 Rheumatic fever HSDN C0011991 Loose stools C0032326 Pneumothorax HSDN C3641755 Have constipation C1869118 Hypothyroidism, congenital, due to thyroid dysgenesis HPO C2188220 Unusual behavior C2220010 Socially inappropriate behavior UMLS C4085317 Diarrhea frequency C0043325 Xanthomatosis HSDN C0424755 Fever symptoms C0276742 Kerion celsi OrphaNet|MalaCards C0012569 Double vision C0023903 Liver neoplasms HSDN C0007815 Cerebrospinal fluid rhinorrhoea C2586211 Thrombosis of blood vessel HSDN C3274924 Have been coughing C0149514 Bronchitis acute MalaCards C4085317 Diarrhea frequency C0221036 Acrodermatitis enteropathica HPO C0522224 Palsied C0034040 Puerperal disorders HSDN C0853986 Lymphocytes decreased C0342701 Transcobalamin ii deficiency OrphaNet|HPO|MalaCards C0004093 Asthenia C0025297 Viral meningitis HSDN C0028738 Nystagmus C2931010 Congenital disorder of glycosylation type 2e MalaCards C3641756 Have diarrhea C0026785 Munchhausen syndrome HSDN C0277799 Fever intermittent C0343068 Familial cold urticaria HPO C0231218 Malaise generalized C1333978 Hepatitis c virus-related hepatocellular carcinoma UMLS C0012569 Double vision C0027121 Myositis HSDN C0009806 Constipate C0003838 Arterial occlusive diseases HSDN C0004604 Pain back C1706377 Memory device component HSDN C0042963 Symptoms vomiting C1855102 Methylmalonic aciduria cblb type HPO|UMLS C0035078 Failure kidney C3889474 Bardet-biedl syndrome 16 MalaCards C1838869 Proximal neurogenic muscle weakness C2678055 Myopathy, x-linked, with postural muscle atrophy (disorder) MalaCards|HPO C2911645 Weight loss adverse event C0020179 Huntington disease HSDN C0023885 Liver abscess C1844376 Granulomatous disease, chronic, x-linked MalaCards C0010520 Skin cyanosis C0003469 Anxiety disorders HSDN C4084726 Distress cough C1253943 Fluid in the chest HSDN C1963252 Tremor adverse event C0017638 Glioma HSDN C0020672 Body temperature decreased C0007193 Cardiomyopathy, dilated HSDN C0002962 Angina C0041227 Trypanosomiasis HSDN C0041657 Consciousness loss C0020651 Hypotension, orthostatic HSDN C2024893 Cardiovascular surgery result: fatigue C0015579 Family characteristics HSDN C4084724 Usual severity constipation C1834211 Ganglioneuromatosis of the alimentary tract HPO C3815497 Cough C1552262 Nurse practitioner - family HSDN C1962972 Proteinuria adverse event C0016057 Fibrosarcoma HSDN C0039070 Collapse fleeting C0018021 Goiter HSDN C4084723 Constipation C1563716 Thyroid dysgenesis HPO C1963087 Constipation adverse event C3276706 Small fiber neuropathy MalaCards C2700617 Irritation - emotion C2932715 Pseudohypoparathyroidism type 1b MalaCards|HPO C0206160 Retic count elevated C0004044 Asphyxia HSDN C0020538 Hbp C0238027 Botulism, infantile OrphaNet|MalaCards C0019079 Bloody sputum C0022658 Kidney diseases HSDN C0042963 Symptoms vomiting C1962986 Glaucoma adverse event HSDN C0262384 Chest pain atypical C0746066 Lung base pulmonary infiltrate UMLS C0000737 Abdomen pain C2987406 Gastric intramucosal adenocarcinoma UMLS C0022346 Yellow skin C0030297 Pancreatic neoplasm MalaCards C0518090 Frequency of pain question C0016665 Fracture, nos with nonunion HSDN C2032395 Pelvic pain on the left C0034065 Pulmonary embolism HSDN C0013456 Pain ear C2239136 Laryngocele HSDN C1963137 Hydrocephalus adverse event C0039743 Thanatophoric dysplasia MalaCards C0018965 Blood urine C0268130 Hereditary orotic aciduria, type 1 MalaCards C0013404 Respiratory difficulty C3148763 Muscular dystrophy, limb-girdle, type 1e MalaCards C0234376 Tremor action C1334410 Localized primitive neuroectodermal tumor MalaCards C0030552 Paralysis partial C0003850 Arteriosclerosis HSDN C0036572 Convulsion C0025281 Meniere disease HSDN C4084775 Usual severity weight loss C0149931 Migraine disorders HSDN C0497406 Over weight C0031212 Personality disorders HSDN C0030193 Sense of pain C0000786 Spontaneous abortion HSDN C0022638 Ketosis C0268575 Isovaleryl-coa dehydrogenase deficiency MalaCards|HPO C0020639 Hypoproteinaemia C2930957 Hantavirosis OrphaNet|MalaCards C4084723 Constipation C1090821 Sepsis (invertebrate) HSDN C2911645 Weight loss adverse event C1847987 Huntington disease-like 2 MalaCards|HPO C0034150 Skin purpura C0030491 Parapsoriasis HSDN C0184567 Pain acute C0010068 Coronary heart disease HSDN C1971624 Appetite absent C0086922 Purpura rheumatoid OrphaNet|MalaCards C0033377 Caudal displacement C0220658 Pfeiffer syndrome OrphaNet|MalaCards C0151686 Growth retardation C1960539 Aromatase deficiency OrphaNet|HPO|MalaCards C0700590 Diaphoresis excessive C0011859 Lipoatrophic diabetes mellitus OrphaNet|HPO C0518090 Frequency of pain question C0005119 Bereavement HSDN C0040485 Wryneck C1865818 Dystonia 7, torsion (disorder) UMLS C2129333 Unreasonable fear of environmental heights C0233701 Height fear UMLS C0151740 Intracranial hypertension C1959582 Pten hamartoma tumor syndrome MalaCards C4084768 Usual severity vomiting C0008625 Chromosome aberrations HSDN C4085210 Usual severity pain C0030290 Fistula pancreatic HSDN C0022346 Yellow skin C3280240 Microcephaly, epilepsy, and diabetes syndrome MalaCards C0015230 Exanthem C0406788 Face - facial afro-caribbean childhood eruption UMLS C2919142 Short stature adverse event C2678312 Three m syndrome 1 OrphaNet|HPO C3887638 Failure to thrive in infant C1835849 Congenital disorder of glycosylation, type im MalaCards|HPO C2984058 Have pain C2936664 Acquired hypogammaglobulinemia HSDN C3146279 Coma C0574108 Glycerol kinase deficiency - isolated MalaCards C0010520 Skin cyanosis C0062527 Hepatitis b vaccine HSDN C0034933 Abnormal reflexes C0033873 Psychiatry HSDN C1963281 Vomiting adverse event C0019159 Hepatitis a DiseaseOntology|HSDN|MalaCards C4085211 Pain distress question C0010678 Cysticercosis HSDN C0035078 Failure kidney C0268425 Alstrom syndrome MalaCards|HPO C1069915 Vertigo C0019360 Herpes zoster disease HSDN C4084776 Weight loss C0016724 Froehlich's syndrome HSDN C0000737 Abdomen pain C0011311 Dengue fever OrphaNet|MalaCards C0917816 Deficiency mental C2936791 Antley-bixler syndrome, autosomal dominant MalaCards C2169806 Tic C4050613 Anxiety scale (basc-2) HSDN C0426579 Anorexia symptom C2984572 Malaria pathway HSDN C2132198 Abnormal blistering of the skin C0032339 Rothmund-thomson syndrome OrphaNet|MalaCards C4084775 Usual severity weight loss C0035242 Respiratory tract diseases HSDN C0424755 Fever symptoms C0021818 Intervertebral disk displacement HSDN C0030193 Sense of pain C0018467 Habituation, psychophysiologic HSDN C2984058 Have pain C0009326 Collagen diseases HSDN C0751837 Gait ataxic C2931859 Acquired cjd MalaCards C0019209 Large liver C1836544 Schindler disease, type i MalaCards|HPO C0042798 Vision dim C3888001 Hermansky-pudlak syndrome 3 MalaCards C3463815 Feel fatigue C0268250 Gaucher disease, type 2 (disorder) MalaCards C0557874 Global developmental delay C2700405 Waardenburg syndrome, type iie HPO C0013404 Respiratory difficulty C0206063 Radiation pneumonitis HSDN C4084774 Have weight loss C0085111 Ankle injury HSDN C0085632 Listlessness C1848916 Tay-sachs disease, variant b1 HPO C0030486 Extremity paralysis, lower C0023801 Lipomatosis HSDN C0518090 Frequency of pain question C0001768 Agammaglobulinemia HSDN C0012833 Dizzy C0033845 Pseudotumor cerebri HSDN C0917816 Deficiency mental C1844005 Hydrocephalus with cerebellar agenesis OrphaNet|MalaCards C3641755 Have constipation C0085655 Polymyositis OrphaNet|MalaCards C0497406 Over weight C0035242 Respiratory tract diseases HSDN C1962972 Proteinuria adverse event C0265275 Jeune thoracic dystrophy MalaCards C1279888 Proteinuria of undiagnosed cause C0021568 Bites insect stings HSDN C0013604 Edematous C0002892 Anemia, pernicious HSDN C1962972 Proteinuria adverse event C3809965 Nephrotic syndrome, type 9 MalaCards C3463815 Feel fatigue C0022336 Creutzfeldt-jakob disease HSDN C0024032 Birth weight subnormal C3279839 Mental retardation, autosomal dominant 7 MalaCards C0034933 Abnormal reflexes C0242422 Parkinsonian disorders HSDN C0037763 Spasm C0015726 Focused anxiety HSDN C0751837 Gait ataxic C0039223 Tabes dorsalis DiseaseOntology|MalaCards C0424755 Fever symptoms C0033289 Family relationship, professional HSDN C0043352 Absent salivary secretion C0748397 Reynolds syndrome OrphaNet|HPO|MalaCards C0011206 Delirium acute C0030569 Secondary parkinson disease HSDN C3146279 Coma C0023418 Leukemia HSDN C1069915 Vertigo C0030286 Pancreatic diseases HSDN C2984058 Have pain C0008513 Chorioretinitis HSDN C0920255 Paresis median nerve C3203709 Peripheral nerve paresis UMLS C0917816 Deficiency mental C3150191 Coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities MalaCards|HPO C0010200 Cough symptom C2973787 Coxiella burnetii infection MalaCards C1962972 Proteinuria adverse event C0007117 Basal cell carcinoma HSDN C0497247 Blood pressure elevation C0265514 Dermatofibrosis lenticularis disseminata MalaCards|HPO C0022346 Yellow skin C0023891 Liver cirrhosis, alcoholic UMLS C3829611 Nausea frequency C0037933 Spinal diseases HSDN C4084776 Weight loss C3469186 Hemochromatosis, type 1 HSDN C1145670 Failure respiratory C3280054 Geleophysic dysplasia 2 MalaCards C1384666 Decreased hearing C1299262 Sarcoma - category (morphologic abnormality) HSDN C0162298 Stiffness joints C1835450 Leri pleonosteosis MalaCards|UMLS C0235153 Sensory hallucination C0543918 Schizophrenia 10 MalaCards C0242936 Center pain C0018023 Nodular goiter HSDN C0557874 Global developmental delay C2931673 Ceroid lipofuscinosis, neuronal 1, infantile MalaCards|HPO C0020538 Hbp C2931426 Orofaciodigital syndrome type1 HPO C0018834 Brash C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO C1963091 Diarrhea adverse event C0014342 Bluecomb of turkeys HSDN C0424755 Fever symptoms C0023048 Creeping eruptions HSDN C2237041 Shox gene with short stature C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0030554 Abnormal sensation C0002448 Ameloblastoma HSDN C4084766 Vomiting C0752132 Infarction, pca HSDN C0002962 Angina C1334928 Necrotic changes (finding) HSDN C0026826 High muscle tone C4084909 Depression subordinate domain HSDN C3463815 Feel fatigue C0008312 Primary biliary cirrhosis MalaCards|HPO C0007859 Pain neck C0085648 Synovial cyst HSDN C4084784 Diarrhea C0005424 Biliary tract diseases HSDN C1557397 Adverse event associated with pain C1265748 Torsion HSDN C4084788 Have dizziness C0700208 Acquired scoliosis HSDN C1963063 Anorexia adverse event C0334409 Leydig cell tumor, benign HSDN C3146279 Coma C0014068 Encephalomalacia HSDN C0027497 Queasy C0009375 Colonic neoplasms HSDN C1963180 Neck pain adverse event C0016542 Foreign body HSDN C4084726 Distress cough C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C0001707 Aerophagia C0013720 Ehlers-danlos syndrome HSDN C0042798 Vision dim C3280428 Alpha-methylacyl-coa racemase deficiency MalaCards C3814530 Skin vesicle C1275114 Epidermolysis bullosa pruriginosa OrphaNet|HPO|MalaCards C0042025 Urinary incontinence stress C4042784 Feeding and eating disorders HSDN C0026821 Cramp C0018824 Heart valve disease HSDN C0476273 Distress respiratory C1849438 Renal dysplasia-limb defects syndrome MalaCards|UMLS C0851578 Disorder sleep C1548578 Location characteristic id - smoking HSDN C0010200 Cough symptom C0178282 Hernia of abdominal cavity HSDN C2237041 Shox gene with short stature C2931226 Thompson baraitser syndrome OrphaNet|MalaCards C3463815 Feel fatigue C0022350 Jaundice, chronic idiopathic MalaCards|HPO C0018681 Headache, cephalalgia C0013806 Electroplexy shock therapy HSDN C4084769 Vomiting frequency C0021368 Inflammation HSDN C4084776 Weight loss C0521585 Gastrointestinal mucositis HSDN C3898969 Have been vomiting C2746068 Congenital idiopathic intestinal pseudoobstruction HPO C4084776 Weight loss C0021295 Infant, premature, diseases HSDN C0026884 Muteness C0860603 Anxiety symptoms HSDN C4085862 Bothered by nausea C0007124 Noninfiltrating intraductal carcinoma HSDN C0033774 Skin pruritus C0009404 Colorectal neoplasms HSDN C1963281 Vomiting adverse event C0043251 Wounds and injuries HSDN C0038002 Spleen enlargement C2936664 Acquired hypogammaglobulinemia MalaCards C1963065 Apnea adverse event C0033923 Psychomotor function HSDN C0043094 Weight gain C0036216 Sarcoma, experimental HSDN C4084727 Cough frequency C0206703 Carcinoma, giant cell HSDN C1557397 Adverse event associated with pain C0150277 Meditations HSDN C0036396 Sciatica C0242013 Neuritis sciatic UMLS C3541349 Syncope C1961100 Erectile dysfunction adverse event HSDN C2024893 Cardiovascular surgery result: fatigue C0483368 Human anaplasmosis due to anaplasma phagocytophilum MalaCards C0024031 Back pain lower back C0038048 Sprains and strains HSDN C4084725 Usual severity cough C0153414 Malignant neoplasm of middle third of esophagus MalaCards C0151786 Weakness muscle C1839566 Charcot-marie-tooth disease, x-linked recessive, 5 OrphaNet|HPO|MalaCards C3829611 Nausea frequency C0018800 Cardiomegaly HSDN C0242936 Center pain C0018567 Hand dermatoses HSDN C1962972 Proteinuria adverse event C0024221 Lymphangioma HSDN C1963170 Hypothermia adverse event C0009375 Colonic neoplasms HSDN C0036572 Convulsion C0001815 Primary myelofibrosis HSDN C0026838 Spasticity muscle C1850597 Leigh syndrome due to mitochondrial complex ii deficiency HPO C0030193 Sense of pain C0038325 Stevens-johnson syndrome HSDN C0030552 Paralysis partial C0086468 Injuries, prenatal HSDN C4084723 Constipation C1253943 Fluid in the chest HSDN C0005779 Clotting C0028326 Noonan syndrome OrphaNet|HPO|MalaCards C2132198 Abnormal blistering of the skin C2930820 Incontinentia pigmenti, familial male lethal type OrphaNet|HPO|MalaCards C0009421 Comatose C0019069 Hemophilia a HSDN C0028738 Nystagmus C0270972 Cornelia de lange syndrome MalaCards|HPO C4084767 Bothered by vomiting C0043251 Wounds and injuries HSDN C0036572 Convulsion C1827389 Epilepsy not intractable UMLS C2096293 Ent surgical result ear vertigo C0032533 Polymyalgia rheumatica MalaCards C4084724 Usual severity constipation C0037073 Sigmoid neoplasms HSDN C4084776 Weight loss C0026850 Muscular dystrophy HSDN C2911645 Weight loss adverse event C0007124 Noninfiltrating intraductal carcinoma HSDN C3641756 Have diarrhea C0026683 Mucocele HSDN C0013395 Indigestion C0019163 Hepatitis b HSDN C4084727 Cough frequency C0016658 Fracture bone HSDN C3887638 Failure to thrive in infant C0206762 Limb deformities, congenital HSDN C0012569 Double vision C0005747 Blepharospasm HSDN C0009676 Confusion state C0034885 Rectal neoplasms HSDN C2700617 Irritation - emotion C1855606 Burton syndrome MalaCards C0014591 Bleeding nose C3150933 Hyperaldosteronism, familial, type iii MalaCards C0035232 Diaphragmatic paralysis C0019284 Diaphragmatic hernia HSDN C0020796 Profoundly mentally retarded C0796232 Bohring syndrome MalaCards|HPO C0015469 Facial paralysis C0854906 Benign schwannoma OrphaNet|MalaCards C0007166 Cardiac output decreased C0919267 Ovarian neoplasm HSDN C0011168 Disorder deglutition C1839780 Fragile x tremor/ataxia syndrome MalaCards|HPO C3887873 Hearing loss C0015934 Fetal growth retardation HSDN C4084802 Usual severity diarrhea C0018482 Haemophilus infections HSDN C4020887 Photodysphoria C0043346 Xeroderma pigmentosum MalaCards|HPO C0015970 Fever unknown origin C3810814 Myocardial infarction ecg assessment HSDN C0007758 Cerebellar ataxia C0027659 Neoplasms, experimental HSDN C0085631 Abnormal excitement C0700327 Clinical findings relating to memory HSDN C0012833 Dizzy C0023895 Liver diseases HSDN C0026884 Muteness C0013010 Cerebral lateralization HSDN C3146279 Coma C0008925 Cleft palate HSDN C1963281 Vomiting adverse event C0403447 Chronic kidney insufficiency HSDN C4084767 Bothered by vomiting C0022602 Actinic keratosis HSDN C0010520 Skin cyanosis C0002880 Autoimmune hemolytic anemia HSDN C0000737 Abdomen pain C0014145 Yolk sac tumor HSDN C4085222 Nausea C2711591 Infection by anisakidae MalaCards C0149793 Transient monocular blindness C2931384 Moyamoya disease 1 HSDN C0575081 Abnormal gait C1858338 Neuropathy, hereditary motor and sensory, okinawa type HPO C0014591 Bleeding nose C0264743 Rheumatic fever without heart involvement MalaCards C4084727 Cough frequency C0013806 Electroplexy shock therapy HSDN C2237041 Shox gene with short stature C1833662 Inclusion body myopathy with early-onset paget disease and frontotemporal dementia MalaCards C2203646 Jaundice C3150672 Arthrogryposis, renal dysfunction, and cholestasis 2 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0344423 Atrial flutter by ecg finding HSDN C4085317 Diarrhea frequency C0023269 Leiomyosarcoma HSDN C1549543 Administration method - pain C0241910 Hepatitis, autoimmune HSDN C1145670 Failure respiratory C0004576 Babesiosis MalaCards C0027066 Myoclonic jerking C1836544 Schindler disease, type i OrphaNet|UMLS|HPO|MalaCards C2315100 Pediatric failure to thrive C1839463 Tarp syndrome MalaCards|HPO C0030975 Disorders perception C0012746 Dissociative disorder HSDN C0036572 Convulsion C3839866 Familial cerebral saccular aneurysm MalaCards C0242936 Center pain C0019069 Hemophilia a HSDN C4084776 Weight loss C0009240 Cognition HSDN C0000737 Abdomen pain C0085083 Ovarian hyperstimulation syndrome OrphaNet|UMLS|HPO|MalaCards C0012833 Dizzy C0015408 Eye injury HSDN C0011570 Monopolar depression C1864851 Pigmented nodular adrenocortical disease, primary, 2 HPO C1963137 Hydrocephalus adverse event C1842870 Chromosome 1p36 deletion syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0039336 Gustatory sense HSDN C0030193 Sense of pain C0524801 Retinal neoplasms HSDN C1963086 Confusion adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084769 Vomiting frequency C0013288 Dumping syndrome HSDN C0043094 Weight gain C0006663 Calcinosis HSDN C0042963 Symptoms vomiting C0020456 Hyperglycemia HSDN C0850758 Pain pelvic C0019553 Contracture hips HSDN C4084776 Weight loss C0021345 Infectious mononucleosis HSDN C4084774 Have weight loss C0030805 Bullous pemphigoid OrphaNet|HPO|MalaCards C2132198 Abnormal blistering of the skin C0406650 Linear iga bullous dermatosis OrphaNet|MalaCards C3641755 Have constipation C0039980 Chest injury HSDN C0012833 Dizzy C0017563 Gingival diseases HSDN C1838579 Pseudobulbar signs C0033790 Pseudobulbar palsy UMLS C0349588 Stature short C3697269 15q24 microdeletion OrphaNet|HPO C0013405 Dyspnea, paroxysmal C2051831 Pectus excavatum HSDN C0004134 Dyssynergia C1956390 Cranial arteritis MalaCards C0413252 Hypothermia due to exposure C1527311 Brain edema HSDN C0344315 Mood depressed C0687720 Central diabetes insipidus OrphaNet|MalaCards C0043094 Weight gain C0022660 Kidney failure, acute HSDN C0023012 Delay language C4014435 Mental retardation, autosomal dominant 26 MalaCards C4084775 Usual severity weight loss C0018800 Cardiomegaly HSDN C1962972 Proteinuria adverse event C2937421 Prostatic hyperplasia HSDN C3829611 Nausea frequency C1962986 Glaucoma adverse event HSDN C0004134 Dyssynergia C0009952 Febrile convulsions HSDN C0000737 Abdomen pain C1516490 Cholangiolocellular carcinoma UMLS C0002962 Angina C0036864 Sexual relations HSDN C1999266 Depression adverse event C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C0008031 Pain chest C0151636 Premature ventricular contractions HSDN C0522224 Palsied C0021833 Intestinal fistula HSDN C0018681 Headache, cephalalgia C3163620 Hypotension adverse event HSDN C4042891 Sleep wake disorders C0012691 Dislocations HSDN C2315100 Pediatric failure to thrive C1856898 Erythroderma lethal congenital OrphaNet|MalaCards C2984057 Have nausea C4085311 Depression - recess HSDN C0851578 Disorder sleep C1690964 Cataract HSDN C1549543 Administration method - pain C0010481 Cushing syndrome HSDN C1963091 Diarrhea adverse event C1546533 Specimen source codes - abscess HSDN C1279888 Proteinuria of undiagnosed cause C0040100 Thymoma HSDN C0043094 Weight gain C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C0000737 Abdomen pain C1332228 Alcohol-related hepatocellular carcinoma UMLS C0010520 Skin cyanosis C0006271 Bronchiolitis HSDN C1963281 Vomiting adverse event C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C0023380 Lethargy C0268543 Hyperammonemia, type iii MalaCards|HPO|UMLS C4084776 Weight loss C1366464 F9 gene HSDN C2024878 Cardiovascular surgery result: dyspnea C1704436 Peripheral arterial diseases HSDN C0000737 Abdomen pain C3888239 Hirschsprung disease, susceptibility to, 1 HSDN C0424755 Fever symptoms C0042344 Varicose ulcer HSDN C2242996 Tingling C0023055 Laryngeal neoplasm HSDN C4084774 Have weight loss C0027121 Myositis HSDN C1384666 Decreased hearing C0265964 Mutilating keratoderma MalaCards|HPO C0242936 Center pain C0867389 Chronic graft-versus-host disease MalaCards C0917816 Deficiency mental C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate OrphaNet|HPO|MalaCards C0237326 Defecation pain C1563706 Nephrogenic diabetes insipidus, type ii HPO C1963281 Vomiting adverse event C0019099 Hemorrhagic fever, crimean DiseaseOntology|MalaCards C4050613 Anxiety C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0034933 Abnormal reflexes C0021890 Intraoperative complications HSDN C0235267 Eye redness C1304456 Congo hemorrhagic fever MalaCards C0917816 Deficiency mental C0795845 Chromosome 12, 12p trisomy OrphaNet|MalaCards C0040264 Ear ringing sound C2586211 Thrombosis of blood vessel HSDN C0242936 Center pain C2004493 Leukemia, b-cell HSDN C1963065 Apnea adverse event C0149931 Migraine disorders HSDN C0016382 Cutaneous vascular engorgement C0457002 Granulomatous slack skin disease OrphaNet|MalaCards C2168170 Intermittent leg claudication C1456822 Claudication (finding) UMLS C0018681 Headache, cephalalgia C0393755 Headache associated with substance abuse or withdrawal UMLS C0002622 Amnesias C1546847 Entity name part type - family HSDN C3887638 Failure to thrive in infant C1856898 Erythroderma lethal congenital OrphaNet|MalaCards C0018991 Paralysis one side of body C0033873 Psychiatry HSDN C0476273 Distress respiratory C1708954 Mediastinal germ cell tumor with somatic-type malignancy UMLS C0013604 Edematous C2188545 Anuria HSDN C3463815 Feel fatigue C0007133 Carcinoma, papillary HSDN C4084725 Usual severity cough C0812393 Cancer patients and suicide and depression HSDN C0043094 Weight gain C0010276 Craniopharyngioma HSDN C0000737 Abdomen pain C1851124 Desmoid disease, hereditary MalaCards C4084725 Usual severity cough C1848814 Thymoma, familial MalaCards C3641756 Have diarrhea C0520946 Emotional hypersensitivity HSDN C0237326 Defecation pain C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C0040264 Ear ringing sound C1962986 Glaucoma adverse event HSDN C0042928 Paralysis vocal cord C0007820 Cerebrovascular disorders HSDN C0020505 Excessive eating C1843792 Frontotemporal lobar degeneration with tdp43 inclusions, grn-related HPO C1549543 Administration method - pain C0338473 Neuroaxonal dystrophies HSDN C0521483 Mucous hyperplasia C0267014 Papillary hyperplasia of palate UMLS C0232493 Epigastric pain C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0020305 Fetal edema C1850510 Sialidosis, type i HPO C0002622 Amnesias C0027927 Neurosyphilis HSDN C0241210 Speaking delay C2675486 Chromosome 6pter p24 deletion syndrome OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0013080 Down syndrome HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2219717 Menstrual periods stopped for over 6 months HSDN C0010200 Cough symptom C0001973 Alcoholic intoxication, chronic HSDN C1963091 Diarrhea adverse event C0206617 Cardiovirus infections HSDN C0011991 Loose stools C0026552 Morphine dependence HSDN C1963091 Diarrhea adverse event C0242350 Erectile dysfunction HSDN C1963170 Hypothermia adverse event C0038941 Incisional infection HSDN C0010200 Cough symptom C0037116 Silicosis HSDN C3274924 Have been coughing C0854421 Hanta viral infections MalaCards C4085210 Usual severity pain C0002880 Autoimmune hemolytic anemia HSDN C0005779 Clotting C1835813 Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency OrphaNet|MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013386 Dyskinesia, drug-induced HSDN C0030552 Paralysis partial C0027809 Neurilemmoma HSDN C1557397 Adverse event associated with pain C0034088 Pulmonary valve insufficiency HSDN C0020672 Body temperature decreased C0029410 Osteoarthritis of hip HSDN C0028738 Nystagmus C1854988 Molybdenum cofactor deficiency, complementation group a HPO C0013604 Edematous C0037228 Size perception HSDN C0035229 Respiratory function impaired C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0017416 Genital neoplasms, female HSDN C1384666 Decreased hearing C1854698 Multiple carboxylase deficiency, juvenile-onset OrphaNet|HPO|MalaCards C0600142 Flash hot C0877792 Sleep disorders, circadian rhythm HSDN C3274924 Have been coughing C0036864 Sexual relations HSDN C0917816 Deficiency mental C0033922 Psychomotor disorders MalaCards C2911645 Weight loss adverse event C0037355 Smallpox vaccines HSDN C1963063 Anorexia adverse event C0004442 Avoidance learning HSDN C0000727 Abdomen acute C0042345 Varicosity HSDN C0035229 Respiratory function impaired C1706595 Pachyonychia congenita, jadassohn lewandowsky type MalaCards C2047953 Illusions recurring without a stimulus C0236816 Stress disorders, traumatic, acute MalaCards C0878773 Bladder hyperactive C1720887 Female urogenital diseases HSDN C1962972 Proteinuria adverse event C0039981 Thoracic neoplasms HSDN C1963086 Confusion adverse event C0007137 Squamous cell carcinoma HSDN C0002622 Amnesias C0009946 Conversion disorder HSDN C0004604 Pain back C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C2911645 Weight loss adverse event C0032310 Pneumonia, viral HSDN C1963071 Back pain adverse event C0033975 Psychotic disorders HSDN C0038002 Spleen enlargement C0242310 Igm heavy chain disease OrphaNet|MalaCards C1962972 Proteinuria adverse event C0403548 Salcedo syndrome MalaCards C0700590 Diaphoresis excessive C2930798 Alexanders leukodystrophy MalaCards C0018681 Headache, cephalalgia C0040830 Fever, five-day DiseaseOntology|MalaCards C3641756 Have diarrhea C0000821 Threatened abortion HSDN C0917816 Deficiency mental C0162635 Angelman syndrome MalaCards C4084767 Bothered by vomiting C0340629 Aortic aneurysm without mention of rupture nos HSDN C0030193 Sense of pain C0221269 Pseudolymphoma HSDN C1963091 Diarrhea adverse event C3150751 Agammaglobulinemia 3, autosomal recessive HPO C0009806 Constipate C2217037 Stage iiia colon cancer UMLS C4084725 Usual severity cough C0264353 Bronchomalacia HSDN C4085548 Usual severity dizziness C0027666 Neoplasms, radiation-induced HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0039236 Tachycardia episodic HSDN C2242996 Tingling C1959620 Dihydropyrimidine dehydrogenase deficiency HSDN C0520966 Coordination impaired C0013364 Dysautonomia, familial HPO|UMLS C0003962 Ascites C1850635 Atrial myxoma, familial MalaCards C0038506 Stutter C0033923 Psychomotor function HSDN C0015469 Facial paralysis C0002726 Amyloidosis OrphaNet|MalaCards C0009806 Constipate C1333085 Colon carcinoma metastatic in the liver UMLS C0020673 Hypothermia (central) (local) C1762616 Meningioma, benign, no icd-o subtype HSDN C0917816 Deficiency mental C1835172 Congenital hypomelanotic and hypermelanotic macules OrphaNet|MalaCards C4084767 Bothered by vomiting C0700327 Clinical findings relating to memory HSDN C0234146 Absent reflex C0699739 Sensory neuropathy, hereditary HPO C0454644 Delayed language development C3553660 Sotos syndrome 2 MalaCards C1557397 Adverse event associated with pain C0043019 Lateral medullary syndrome HSDN C4085211 Pain distress question C0018920 Hemangioma, cavernous HSDN C0015300 Ocular proptosis C1856159 Urioste martinez-frias syndrome MalaCards C0332563 Papulae C1275114 Epidermolysis bullosa pruriginosa OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0206723 Sertoli-leydig cell tumor HSDN C0393765 24 hour hypersomnolence C0917799 Hypersomnia UMLS C4084768 Usual severity vomiting C1509147 Histiocytoma HSDN C2127294 Fainting preceded by seeing a spider C0340849 Fainting simple UMLS C1069915 Vertigo C1868649 Panic disorder 1 HSDN C4084802 Usual severity diarrhea C0041948 Uremia HSDN C0037763 Spasm C0751895 Vasospasm, intracranial HSDN C0004134 Dyssynergia C0007781 Intracranial embolism and thrombosis HSDN C0042571 Vertigo subjective C0019699 Hiv seropositivity HSDN C2024893 Cardiovascular surgery result: fatigue C0017168 Gastroesophageal reflux disease HSDN C4084726 Distress cough C0032453 Polychondritis, relapsing OrphaNet|MalaCards C0020580 Decreased sensation C0022661 Kidney failure, chronic HSDN C3887638 Failure to thrive in infant C1849157 Insulin-like growth factor i, resistance to MalaCards C0023530 Leukopenia C0398689 Hyper-igm immunodeficiency syndrome, type 1 HPO C0011991 Loose stools C0282607 Vascular neoplasms HSDN C0000737 Abdomen pain C0344435 Ventricular fibrillation by ecg finding HSDN C0009676 Confusion state C0021361 Female infertility HSDN C0151686 Growth retardation C0033300 Progeria OrphaNet|HPO C4085317 Diarrhea frequency C0032326 Pneumothorax HSDN C2984058 Have pain C0032310 Pneumonia, viral HSDN C0027498 Nausea vomiting C0024623 Malignant neoplasm of stomach UMLS C0036572 Convulsion C3815186 Ager wt allele HSDN C1962972 Proteinuria adverse event C0018273 Growth disorders HSDN C0036572 Convulsion C0268386 Amyloid polyneuropathy, swiss type MalaCards C0013604 Edematous C0036986 Shock, traumatic HSDN C0003467 Angst C0268322 Chester-type porphyria HPO C3539022 Pelvic pain decreasing in severity C0563150 Catastrophization HSDN C0009421 Comatose C0031511 Pheochromocytoma HSDN C2024878 Cardiovascular surgery result: dyspnea C0020676 Hypothyroidism HSDN C0878638 Tongue signs C2930852 Zellweger leukodystrophy MalaCards C2984058 Have pain C0428478 Serum triglycerides raised HSDN C0012833 Dizzy C0268338 Ehlers-danlos syndrome, type iv HPO C0036572 Convulsion C0595948 Atypical absence seizure UMLS C4084725 Usual severity cough C0018944 Hematoma HSDN C4084768 Usual severity vomiting C0282207 Cronkhite-canada syndrome MalaCards C3539020 Pelvic pain decreasing in frequency C0600041 Infective cystitis HSDN C4084774 Have weight loss C0022134 Islet cell adenoma HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0024232 Lymphatic metastasis HSDN C4085210 Usual severity pain C0042216 Poxvirus officinalis HSDN C0150045 Urinary incontinence urge C0238190 Inclusion body myositis (disorder) HSDN C0011991 Loose stools C0006277 Bronchitis HSDN C1971624 Appetite absent C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C0085128 Cardiac output elevated C0022739 Klippel-trenaunay-weber syndrome HSDN C0019079 Bloody sputum C0034068 Pulmonary eosinophilia HSDN C2911647 Weight gain adverse event C0007273 Carotid artery diseases HSDN C0727671 Red cross toothache drops C0042138 Uterine neoplasms HSDN C1000483 Genus anemia C1846979 Senior-loken syndrome 4 MalaCards|HPO C2911645 Weight loss adverse event C0153414 Malignant neoplasm of middle third of esophagus MalaCards C4085642 Level of joint stiffness C1861313 Synostosis, carpal, with dysplastic elbow joints and brachydactyly MalaCards C0522224 Palsied C0002792 Anaphylaxis HSDN C4085222 Nausea C0035435 Rheumatism HSDN C4085317 Diarrhea frequency C0027947 Neutropenia HSDN C0018926 Emesis bloody C0006262 Bronchial fistula HSDN C4084784 Diarrhea C1739094 Foodborne botulism OrphaNet|MalaCards C0848203 Male pelvic pain C1547940 Specimen source codes - ulcer HSDN C0019079 Bloody sputum C0035204 Respiration disorders HSDN C2032395 Pelvic pain on the left C0016542 Foreign body HSDN C2984058 Have pain C0020097 Htlv-i infections HSDN C1000483 Genus anemia C1855102 Methylmalonic aciduria cblb type HPO C0006370 Bulimia C0009395 Color perception HSDN C1971624 Appetite absent C0037274 Dermatologic disorders HSDN C0027066 Myoclonic jerking C0017563 Gingival diseases HSDN C0019572 Hairiness C2930971 Acroosteolysis dominant type MalaCards C0700078 Deep tendon reflex decrease C0271865 Autoimmune hypoparathyroidism MalaCards C4084766 Vomiting C0002994 Angioedema HSDN C0242936 Center pain C0014145 Yolk sac tumor HSDN C0240682 Pelvic girdle pain C0024919 Behavior, maternal HSDN C1963064 Anxiety adverse event C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C1971624 Appetite absent C0033348 Language program HSDN C0000737 Abdomen pain C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0018772 Deafness C0042826 Field visual HSDN C0349588 Stature short C0268242 Niemann-pick disease, type a MalaCards|HPO C4084802 Usual severity diarrhea C0036421 Systemic scleroderma HSDN C1856661 Cornea cloudy C0265201 De sanctis-cacchione syndrome MalaCards C1963281 Vomiting adverse event C0024530 Malaria HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2051831 Pectus excavatum HSDN C0009421 Comatose C0014121 Bacterial endocarditis HSDN C0033774 Skin pruritus C1867981 Porokeratosis, disseminated superficial actinic, 1 MalaCards C0349588 Stature short C3280598 Short-rib thoracic dysplasia 5 with or without polydactyly MalaCards C0010200 Cough symptom C0007273 Carotid artery diseases HSDN C2036545 Stuttering interfering with talking on telephone C0038506 Stuttering UMLS C0018772 Deafness C0012655 Disease susceptibility HSDN C0039070 Collapse fleeting C0018767 Auditory sense HSDN C0035078 Failure kidney C0300948 Caudal regression syndrome HPO C1963086 Confusion adverse event C0021603 Sleep initiation and maintenance disorders HSDN C0019209 Large liver C1832615 Hyperparathyroidism, neonatal severe OrphaNet|HPO C0028738 Nystagmus C1852438 Cataract, coppock-like MalaCards|HPO C3274924 Have been coughing C0028758 Bonding HSDN C0002963 Angina variant C0018799 Heart diseases HSDN C1963184 Nystagmus adverse event C0268140 Xeroderma pigmentosum, group f HPO C0574002 Foot swelling C0239340 Edema of lower extremity UMLS C0040485 Wryneck C0021368 Inflammation HSDN C3887873 Hearing loss C0520946 Emotional hypersensitivity HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0020435 Hyperbilirubinemia, hereditary HSDN C4084776 Weight loss C0035869 Rotavirus infections HSDN C0917816 Deficiency mental C1864186 Cdags syndrome OrphaNet|MalaCards C0037383 Sneeze C2186740 Reported urticaria HSDN C3541349 Syncope C0022758 Kap HSDN C3641755 Have constipation C0036357 Psychology, schizophrenic HSDN C2984058 Have pain C2240374 Eosinophil count raised HSDN C1963091 Diarrhea adverse event C0034013 Precocious puberty HSDN C0002965 Crescendo angina C0007282 Carotid stenosis HSDN C2911645 Weight loss adverse event C0085435 Arthritis, reactive MalaCards C1384666 Decreased hearing C0265449 Pallister-killian syndrome MalaCards C1963184 Nystagmus adverse event C1844579 Exudative vitreoretinopathy, familial, x-linked recessive MalaCards|HPO C0019572 Hairiness C0020481 Hyperlipoproteinemia type v HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0026857 Musculoskeletal diseases HSDN C1260880 Nasal drip C1708603 Keratinizing paranasal sinus squamous cell carcinoma UMLS C0085636 Light sensitivity C1847836 Oculocutaneous albinism, type iv OrphaNet|HPO|MalaCards C0033377 Caudal displacement C2678439 Cranioosteoarthropathy HPO C1565249 Limitation, mobility C0236969 Substance-related disorders HSDN C1549543 Administration method - pain C0029423 Cartilaginous exostosis HSDN C0035229 Respiratory function impaired C0271829 Pendred's syndrome MalaCards|HPO C0007758 Cerebellar ataxia C1963137 Hydrocephalus adverse event HSDN C0019079 Bloody sputum C0280391 Stage iv squamous cell carcinoma of the hypopharynx UMLS C1963281 Vomiting adverse event C2240378 Cleft palate on exam HSDN C0037316 Not enough sleeping C0004935 Animal ethology HSDN C1962956 Flatulence adverse event C1720887 Female urogenital diseases HSDN C0151818 Opisthotonos C3151140 Pontocerebellar hypoplasia, type 2d MalaCards C0033774 Skin pruritus C0263221 Acute eczema UMLS C4084766 Vomiting C1855849 Bartter syndrome, antenatal , type 2 HPO C0349588 Stature short C1860991 Noonan syndrome 3 MalaCards|HPO C0520909 Ponv C0042138 Uterine neoplasms HSDN C0040485 Wryneck C0004936 Mental disorders HSDN C4085211 Pain distress question C0017160 Gastroenteritis HSDN C0036572 Convulsion C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0085642 Asphyxia reticularis C1959632 Plasma cell neoplasm HSDN C0750937 Appendicular ataxia C1853249 Spinocerebellar ataxia 28 MalaCards|HPO C0727671 Red cross toothache drops C0021268 Inert gas narcosis HSDN C0022346 Yellow skin C1518868 Pancreatic intraductal papillary mucinous adenoma UMLS C0035229 Respiratory function impaired C0205711 Pelizaeus-merzbacher disease OrphaNet|MalaCards C1963170 Hypothermia adverse event C0013080 Down syndrome HSDN C0010200 Cough symptom C0342257 Complications of diabetes mellitus HSDN C4042891 Sleep wake disorders C4049994 Insulin resistance measurement HSDN C0022346 Yellow skin C2931132 Crigler najjar syndrome, type 2 MalaCards|UMLS C0002962 Angina C0007766 Intracranial aneurysm HSDN C0007166 Cardiac output decreased C0037315 Sleep apnea syndromes HSDN C4084766 Vomiting C0027092 Myopia HSDN C0028738 Nystagmus C4015505 Spinocerebellar ataxia, autosomal recessive 18 MalaCards C1557397 Adverse event associated with pain C0024841 Matrimony, matrimonial HSDN C1962957 Flushing adverse event C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0042963 Symptoms vomiting C0268547 Argininosuccinic aciduria MalaCards|HPO|UMLS C1549543 Administration method - pain C0014118 Endocarditis HSDN C0018772 Deafness C0003467 Anxiety HSDN C3641755 Have constipation C0271585 Isolated trh deficiency MalaCards C4049602 Hyperactivity C3806730 Mental retardation, x-linked 98 MalaCards C0018524 Hallucinate C1552527 Clinic / center - developmental disabilities HSDN C0027498 Nausea vomiting C0151467 Addisonian crisis OrphaNet|MalaCards C0041657 Consciousness loss C0161398 Neuropathy optic traumatic HSDN C2984058 Have pain C0030521 Parathyroid neoplasms HSDN C1549543 Administration method - pain C0014009 Empyema HSDN C1557397 Adverse event associated with pain C0011880 Diabetic ketoacidosis HSDN C0020673 Hypothermia (central) (local) C0026946 Mycoses HSDN C0012833 Dizzy C0022665 Kidney neoplasm HSDN C0020538 Hbp C1857553 Hsd11b2, arg208cys HPO C4084775 Usual severity weight loss C0021071 Immunoproliferative small intestinal disease HSDN C2911645 Weight loss adverse event C0020522 Delayed hypersensitivity HSDN C0233514 Behavior abnormal C0220992 Histidinemia MalaCards C3829611 Nausea frequency C0026848 Myopathy HSDN C3641755 Have constipation C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C0037763 Spasm C0858719 Tetanic spasm generalised UMLS C0349588 Stature short C1856492 Gaucher disease, type iiib HPO C0013604 Edematous C0005779 Blood coagulation disorders HSDN C1279888 Proteinuria of undiagnosed cause C0019693 Hiv infections HSDN C1971624 Appetite absent C0162637 Strongylida infections HSDN C0008031 Pain chest C0162576 Anisakiasis HSDN C0151786 Weakness muscle C0003467 Anxiety HSDN C4084802 Usual severity diarrhea C0018923 Hemangiosarcoma HSDN C3146279 Coma C0153065 Eastern equine encephalomyelitis DiseaseOntology|MalaCards C4084773 Bothered by weight gain C0439840 Reflex motion descriptor HSDN C0917816 Deficiency mental C0035334 Retinitis pigmentosa OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C1867396 Radial-renal syndrome MalaCards C0013604 Edematous C0162834 Hyperpigmentation HSDN C0006370 Bulimia C0004377 Automatism HSDN C1963091 Diarrhea adverse event C0238462 Medullary carcinoma of thyroid OrphaNet C0024031 Back pain lower back C0036323 Schistosomiasis HSDN C0030552 Paralysis partial C0015625 Fanconi anemia HSDN C1549543 Administration method - pain C0037930 Spinal cord neoplasms HSDN C1279888 Proteinuria of undiagnosed cause C0029434 Osteogenesis imperfecta HSDN C2203646 Jaundice C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0600142 Flash hot C1176475 Ductal carcinoma HSDN C4084767 Bothered by vomiting C1367460 Lats1 gene HSDN C0020438 Hypercalciuria C0314657 Genetic predisposition HSDN C0413252 Hypothermia due to exposure C1510412 Pseudoaneurysm HSDN C3829611 Nausea frequency C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0018834 Brash C0265498 48, xxxy syndrome MalaCards C0522224 Palsied C0003125 Anorexia nervosa HSDN C0008031 Pain chest C0029443 Osteomyelitis HSDN C0424755 Fever symptoms C0035869 Rotavirus infections HSDN C0011991 Loose stools C0000809 Abortion, habitual HSDN C4084726 Distress cough C0037051 Behavior illness HSDN C2237041 Shox gene with short stature C0685837 Pure gonadal dysgenesis, 46, xx HPO C0036572 Convulsion C0033117 Priapism HSDN C4084727 Cough frequency C0206628 Mesoblastic nephroma HSDN C0015672 Decreased energy C3714514 Infection HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0040954 Infection by trichuris trichiura HSDN C1971624 Appetite absent C0017160 Gastroenteritis DiseaseOntology C1961131 Cough adverse event C0036341 Schizophrenia HSDN C0026838 Spasticity muscle C3502054 Dentoleukoencephalopathy MalaCards C1963091 Diarrhea adverse event C0206526 Tuberculosis, multidrug-resistant HSDN C0042571 Vertigo subjective C1690964 Cataract HSDN C4042891 Sleep wake disorders C0007766 Intracranial aneurysm HSDN C0031911 Pigment deposition C3539123 Ceroid lipofuscinosis, neuronal, 11 MalaCards C4084788 Have dizziness C0011989 Camurati-engelmann syndrome HSDN C0026603 Motion sickness C0270611 Brain damage HSDN C1069915 Vertigo C0018798 Congenital heart defects HSDN C0917816 Deficiency mental C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards|HPO C1069915 Vertigo C0024141 Lupus erythematosus, systemic HSDN C4084724 Usual severity constipation C0029456 Osteoporosis HSDN C0242936 Center pain C0005689 Bladder exstrophy HSDN C3898969 Have been vomiting C3150895 Chromosome 19p13.13 duplication syndrome MalaCards C2045681 Change in urinary habits C0152032 Hesitancy urination UMLS C0000737 Abdomen pain C1335377 Periampullary adenocarcinoma UMLS C3898969 Have been vomiting C0035439 Rheumatic heart disease HSDN C0162285 Edema eyelid C1848814 Thymoma, familial MalaCards C4084769 Vomiting frequency C0025149 Medulloblastoma HSDN C1963065 Apnea adverse event C0003838 Arterial occlusive diseases HSDN C4085862 Bothered by nausea C0009450 Disease caused by microorganism HSDN C0013421 Dystonia C0007097 Carcinomas HSDN C0040264 Ear ringing sound C0040034 Thrombocytopenia HSDN C0231623 Femoral neuralgia C0751931 Femoral lesion nerve UMLS C4042891 Sleep wake disorders C0042164 Uveitis HSDN C0040485 Wryneck C1857495 Cardiocranial syndrome MalaCards C1384666 Decreased hearing C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0030193 Sense of pain C0020445 Hypercholesterolemia, familial HSDN C3494358 Characteristic, prodromal C1384671 Mros gene HSDN C4020887 Photodysphoria C0432267 Tricho thiodystrophy disorder MalaCards C0518090 Frequency of pain question C0019061 Hemolytic-uremic syndrome HSDN C0012833 Dizzy C0032285 Pneumonia HSDN C4085548 Usual severity dizziness C0023290 Leishmaniasis, visceral HSDN C0036572 Convulsion C0544862 Neurocutaneous melanosis OrphaNet|HPO C0015672 Decreased energy C0006413 Burkitt lymphoma HSDN C0398650 Idiopathic thrombocytopenia purpura C0043251 Wounds and injuries HSDN C2919142 Short stature adverse event C0079154 Congenital nonbullous ichthyosiform erythroderma MalaCards|HPO C0020458 Hyperhydrosis C3502298 Lactic acidosis, fatal infantile MalaCards C0344434 Atrial fibrillation ecg C4015368 Aortic aneurysm, familial thoracic 9 MalaCards C3641756 Have diarrhea C0023281 Leishmaniasis HSDN C0002962 Angina C0012644 Animal disease models HSDN C0010520 Skin cyanosis C0022107 Irritable mood HSDN C0242936 Center pain C0013298 Duodenitis HSDN C0009792 Consciousness disorder C0032290 Aspiration pneumonia HSDN C4085862 Bothered by nausea C0020542 Pulmonary hypertension HSDN C0242936 Center pain C0006131 Branchioma HSDN C1962972 Proteinuria adverse event C2931872 Free sialic acid storage disease MalaCards C0860603 Anxiety symptom C0751434 Classical phenylketonuria MalaCards|HPO C0015469 Facial paralysis C0751803 Brain stem hemorrhage, post traumatic HSDN C4085211 Pain distress question C0037313 Sleep HSDN C0042024 Urine incontinence C0033975 Psychotic disorders HSDN C2984057 Have nausea C0002871 Anemia HSDN C0242936 Center pain C0020514 Hyperprolactinemia HSDN C0002962 Angina C0019655 Histoplasmosis HSDN C3539891 Pelvic pain to the rear C0221752 Rbc urine HSDN C0007166 Cardiac output decreased C0027765 Nervous system disorder HSDN C4084774 Have weight loss C0206743 Rhabdoid tumor OrphaNet|MalaCards C1963091 Diarrhea adverse event C0023798 Lipoma HSDN C4085210 Usual severity pain C0015328 Behavior, exploratory HSDN C4084723 Constipation C0005967 Bone neoplasms HSDN C2096293 Ent surgical result ear vertigo C0597109 Nurse's role HSDN C4084766 Vomiting C1959626 Mevalonic aciduria MalaCards|HPO C2984057 Have nausea C0878544 Cardiomyopathies HSDN C0497406 Over weight C4084909 Depression subordinate domain HSDN C0020455 Hypergammaglobulinemia C0027121 Myositis HSDN C0007166 Cardiac output decreased C0002395 Alzheimer's disease HSDN C0018772 Deafness C0017178 Gastrointestinal diseases HSDN C0557874 Global developmental delay C0431350 Primary microcephaly MalaCards C0042023 Urination frequency C3150878 Hyperoxaluria, primary, type iii MalaCards C0850758 Pain pelvic C0029400 Osteitis HSDN C0151686 Growth retardation C0733682 Hypophosphatemic rickets, x-linked dominant MalaCards C0036659 Sensation disorder C0035258 Restless legs syndrome HSDN C3665346 Loss sight C0242387 Mandibulofacial dysostosis MalaCards|HPO C4084774 Have weight loss C0019284 Diaphragmatic hernia HSDN C0030486 Extremity paralysis, lower C0032914 Pre-eclampsia HSDN C0002962 Angina C0001621 Adrenal gland diseases HSDN C1549543 Administration method - pain C0037275 Skin diseases, vesiculobullous HSDN C0002962 Angina C0032965 Pregnancy complications, infectious HSDN C0812426 Kidney problem C0027707 Nephritis, interstitial UMLS C3887638 Failure to thrive in infant C0342273 Transient neonatal diabetes mellitus MalaCards C0007758 Cerebellar ataxia C4041080 Neurocognitive disorders HSDN C0003113 Anomia C0233629 Thinking and speaking disturbances HSDN C0262384 Chest pain atypical C0086769 Panic attacks UMLS C0030193 Sense of pain C0221391 Melanosis coli HSDN C0015672 Decreased energy C0020649 Hypotension HSDN C4085211 Pain distress question C0036980 Shock, cardiogenic HSDN C0014089 Functional encopresis C0003477 Separation anxiety disorder HSDN C0028738 Nystagmus C0752166 Bardet-biedl syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0221752 Rbc urine HSDN C4085549 Dizziness C0155490 Middle ear cholesteatoma HSDN C3829611 Nausea frequency C0997768 Glaucoma HSDN C4084802 Usual severity diarrhea C0037937 Spine injury HSDN C2024893 Cardiovascular surgery result: fatigue C0376545 Hematologic neoplasms HSDN C4085549 Dizziness C0853697 Neutrophil count decreased HSDN C0016204 Fart C0004275 Attitude health HSDN C4084802 Usual severity diarrhea C0024419 Waldenstrom macroglobulinemia MalaCards|HPO C0241210 Speaking delay C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO C0039239 Tachycardia sinus C0221056 Adult type dermatomyositis MalaCards C0424755 Fever symptoms C0034089 Pulmonary valve stenosis HSDN C0234132 Pyramidal sign C2936910 Cross-mckusick-breen syndrome OrphaNet|MalaCards C0746674 Muscle weakness generalized C0022134 Islet cell adenoma MalaCards C2237041 Shox gene with short stature C1836121 Al-gazali syndrome MalaCards C1384666 Decreased hearing C3808981 Hypogonadotropic hypogonadism 19 with or without anosmia MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0872996 Q fever vaccine HSDN C4049644 Depression C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0476273 Distress respiratory C0268596 Multiple acyl coenzyme a dehydrogenase deficiency HPO C0042571 Vertigo subjective C0030567 Parkinson disease HSDN C3641756 Have diarrhea C0025064 Mediastinitis HSDN C2984058 Have pain C0025637 Methemoglobinemia HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0021783 Internal external locus of control HSDN C4084776 Weight loss C0041324 Tuberculosis, osteoarticular HSDN C0020649 Blood pressure decreased C1846343 Bartter syndrome, type 3 MalaCards|HPO C4085210 Usual severity pain C0020540 Malignant hypertension HSDN C0009806 Constipate C0028860 Oculocerebrorenal syndrome OrphaNet|HPO|UMLS C0040822 D tremors C0008924 Cleft lip HSDN C0011206 Delirium acute C0023890 Liver cirrhosis HSDN C4084784 Diarrhea C1704272 Benign prostatic hyperplasia HSDN C0857305 Thrombocytopenia purpura C0025202 Melanoma HSDN C0917816 Deficiency mental C3888244 Aicardi-goutieres syndrome 7 MalaCards C0013390 Cramps menstrual C0032460 Polycystic ovary syndrome HSDN C0015672 Decreased energy C1546533 Specimen source codes - abscess HSDN C0038002 Spleen enlargement C0334634 Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse MalaCards C0085602 Polydypsia C0393665 Multiple sclerosis, chronic progressive HSDN C0002965 Crescendo angina C0037928 Spinal cord diseases HSDN C0033377 Caudal displacement C1843225 Charcot-marie-tooth disease, axonal, type 2e (disorder) HPO C1961131 Cough adverse event C0279626 Squamous cell carcinoma of esophagus OrphaNet|HPO|MalaCards C0587246 Extremity weakness C1836447 Nemaline myopathy 4 HPO C0042025 Urinary incontinence stress C0001430 Adenoma HSDN C0030193 Sense of pain C0041316 Lymph node tuberculosis HSDN C0332563 Papulae C0544799 Histiocytosis, generalized eruptive MalaCards C0020538 Hbp C0432442 Chromosome 18p deletion syndrome OrphaNet|MalaCards C4085549 Dizziness C1510412 Pseudoaneurysm HSDN C2024878 Cardiovascular surgery result: dyspnea C0021655 Insulin resistance HSDN C2024878 Cardiovascular surgery result: dyspnea C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C0424755 Fever symptoms C0026766 Multiple organ failure HSDN C0424755 Fever symptoms C0013473 Eating disorders HSDN C0042798 Vision dim C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0033377 Caudal displacement C1853249 Spinocerebellar ataxia 28 MalaCards|HPO C0034933 Abnormal reflexes C1458155 Mammary neoplasms HSDN C1145670 Failure respiratory C0024776 Maple syrup urine disease OrphaNet C0036572 Convulsion C0796122 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome OrphaNet|MalaCards C0019079 Bloody sputum C0262584 Carcinoma, small cell HSDN C0030193 Sense of pain C0019372 Herpesviridae infections HSDN C2242996 Tingling C0017181 Gastrointestinal hemorrhage HSDN C1145670 Failure respiratory C2675526 Neutropenia, severe congenital, autosomal recessive 4 HPO C0023012 Delay language C3806403 Continuous spike and waves during slow-wave sleep syndrome MalaCards C1279888 Proteinuria of undiagnosed cause C1853124 Nephrotic syndrome, type 3 MalaCards|HPO C4084802 Usual severity diarrhea C0235387 Porphyria type syndrome OrphaNet C0022346 Yellow skin C0007097 Carcinomas HSDN C4085211 Pain distress question C0029927 Ovarian cysts HSDN C0037763 Spasm C0175713 Aicardi's syndrome HSDN C1279888 Proteinuria of undiagnosed cause C0403548 Salcedo syndrome MalaCards C0011991 Loose stools C0006057 Botulisms MalaCards C0028738 Nystagmus C3645711 Congenital osteopetrosis MalaCards C4084802 Usual severity diarrhea C0016667 Fragile x syndrome HSDN C0019521 Hiccoughs C1999266 Depression adverse event HSDN C0013395 Indigestion C0026266 Mitral valve insufficiency HSDN C3665492 Pigmentations C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0007758 Cerebellar ataxia C0014378 Enterovirus infections HSDN C0023380 Lethargy C0001624 Adrenal gland neoplasms HSDN C0241137 Skin pallor C0268608 Deficiency of dihydrofolate reductase MalaCards C1069915 Vertigo C0023267 Fibroid tumor HSDN C0013390 Cramps menstrual C0023903 Liver neoplasms HSDN C0917816 Deficiency mental C1842577 Joubert syndrome 2 MalaCards|HPO C2315100 Pediatric failure to thrive C0342784 Pearson's marrow-pancreas syndrome OrphaNet|MalaCards C4085211 Pain distress question C0011253 Delusions HSDN C3463815 Feel fatigue C0006145 Breast diseases HSDN C0010200 Cough symptom C1332337 Asbestos-related lung carcinoma UMLS C4084767 Bothered by vomiting C0041228 African trypanosomiasis HSDN C0237326 Defecation pain C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C4084768 Usual severity vomiting C0027809 Neurilemmoma HSDN C4084727 Cough frequency C3887494 Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0020673 Hypothermia (central) (local) C2984291 Glioblastoma multiforme pathway HSDN C4085211 Pain distress question C0034884 Rectal fistula HSDN C4084802 Usual severity diarrhea C0024282 Lymphocytosis HSDN C2984057 Have nausea C0006434 Burn injury HSDN C1963071 Back pain adverse event C0007097 Carcinomas HSDN C0040264 Ear ringing sound C0015745 Ingestive behavior HSDN C0003811 Cardiac rhythm disturbance C1306794 Wound botulism MalaCards C0018991 Paralysis one side of body C0019829 Hodgkin disease HSDN C0476273 Distress respiratory C0853240 Mobius ii syndrome MalaCards C0349588 Stature short C1866505 Ichthyosis, congenital, with trichothiodystrophy HPO C0428977 Pulse rate decrease C1970298 Progressive familial heart block, type ib MalaCards|HPO C2315100 Pediatric failure to thrive C0206641 Osteochondromatosis OrphaNet|HPO C2315100 Pediatric failure to thrive C3151113 Meier-gorlin syndrome 3 MalaCards|HPO C1145670 Failure respiratory C0040100 Thymoma MalaCards C0030552 Paralysis partial C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C4085210 Usual severity pain C0546983 Post-concussion syndrome HSDN C0518090 Frequency of pain question C0025490 Mesonephroma HSDN C0018681 Headache, cephalalgia C0038273 Stereotypic movement disorder HSDN C0030193 Sense of pain C1963164 Lymphopenia adverse event HSDN C1510456 Wernicke aphasia C0011265 Presenile dementia HSDN C0026826 High muscle tone C0795949 Galloway mowat syndrome MalaCards|HPO C4084776 Weight loss C0032131 Plasmacytoma HSDN C0023015 Language handicap C0032897 Prader-willi syndrome HSDN C0003862 Pain joint C0003708 Arachnitis OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0270611 Brain damage HSDN C0015230 Exanthem C0263603 Polymorphous light eruption, eczematous type UMLS C0000727 Abdomen acute C0019163 Hepatitis b HSDN C0036659 Sensation disorder C1090821 Sepsis (invertebrate) HSDN C0030975 Disorders perception C0008626 Congenital chromosomal disease HSDN C0018681 Headache, cephalalgia C0242383 Age related macular degeneration HSDN C1557397 Adverse event associated with pain C0029139 Optical illusion HSDN C0036572 Convulsion C0025874 Metrorrhagia HSDN C1549543 Administration method - pain C0161406 Injury nerve trigeminal HSDN C0039231 Heartbeats increased C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C1961131 Cough adverse event C0003962 Ascites HSDN C1963063 Anorexia adverse event C0007784 Cerebral hemisphere hemorrhage HSDN C0040822 D tremors C0027819 Neuroblastoma HSDN C2984058 Have pain C0032816 Post-concussion headache HSDN C1145670 Failure respiratory C0036069 Saldino-noonan syndrome MalaCards C0398650 Idiopathic thrombocytopenia purpura C0035305 Retinal detachment HSDN C0036572 Convulsion C1865639 Gracile bone dysplasia MalaCards|HPO|UMLS C3641755 Have constipation C0423742 Intercourse pain HSDN C0242936 Center pain C0040947 Trichostrongyloidiasis HSDN C0013604 Edematous C0030470 Paranasal sinus neoplasms HSDN C2984058 Have pain C0008519 Ectopic tissue HSDN C1962972 Proteinuria adverse event C1302282 Chromaffin cell neoplasm MalaCards C0413252 Hypothermia due to exposure C0597109 Nurse's role HSDN C1963177 Muscle pain adverse event C3276706 Small fiber neuropathy MalaCards C2203646 Jaundice C0010823 Cytomegalovirus infections HSDN C4084769 Vomiting frequency C0153064 Encephalomyelitis, western equine DiseaseOntology|MalaCards C1963065 Apnea adverse event C0460137 Push down or depress HSDN C2203646 Jaundice C0019202 Hepatolenticular degeneration OrphaNet|HPO|MalaCards C3829611 Nausea frequency C0033817 Pseudomonas infections HSDN C0917816 Deficiency mental C0265497 Chromosome xxxxx syndrome OrphaNet|MalaCards C4084724 Usual severity constipation C0038160 Staphylococcal infections HSDN C0033774 Skin pruritus C0032708 Disorders of porphyrin metabolism OrphaNet|MalaCards C1557397 Adverse event associated with pain C0024440 Macular edema, cystoid HSDN C0012833 Dizzy C0022661 Kidney failure, chronic HSDN C1557397 Adverse event associated with pain C0003460 Anurias HSDN C0022107 Fussiness C0268547 Argininosuccinic aciduria MalaCards|HPO C1963247 Ventricular tachycardia adverse event C1834481 Cardiomyopathy, dilated, 1s MalaCards C0015402 Hemorrhage eye C0024214 Lymphangiectasis HSDN C1850830 Exercise-induced muscle pain C1838254 Rippling muscle disease 1 MalaCards|UMLS C2048468 Inability to impregnate C0403814 Congenital bilateral aplasia of vas deferens OrphaNet|HPO C0003910 Articulation disorder C0033324 Prognathism HSDN C0024031 Back pain lower back C0021845 Intestinal perforation HSDN C4042891 Sleep wake disorders C0008625 Chromosome aberrations HSDN C0020673 Hypothermia (central) (local) C0033923 Psychomotor function HSDN C0344307 Analgesia C1835671 Axonal neuropathy with palmoplantar keratoderma MalaCards C0424755 Fever symptoms C0038273 Stereotypic movement disorder HSDN C0016382 Cutaneous vascular engorgement C0343056 Acute generalized pustular psoriasis MalaCards C0497247 Blood pressure elevation C0265915 Congenital stenosis, pulmonary veins OrphaNet|MalaCards C2911645 Weight loss adverse event C0026848 Myopathy HSDN C4084773 Bothered by weight gain C0010276 Craniopharyngioma HSDN C0003862 Pain joint C0265235 Marshall syndrome OrphaNet|HPO|MalaCards C0018524 Hallucinate C0033800 Pseudoglioma MalaCards C4085317 Diarrhea frequency C0013575 Ectodermal dysplasia HSDN C1384666 Decreased hearing C0085426 Gram-positive bacterial infections HSDN C0026838 Spasticity muscle C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C3641755 Have constipation C0023343 Leprosy HSDN C4084769 Vomiting frequency C1868649 Panic disorder 1 HSDN C3641756 Have diarrhea C2939465 Deficiency of glucose-6-phosphate dehydrogenase HSDN C0000731 Abdomen distention C0266833 Visceral myopathy, familial OrphaNet|HPO|MalaCards C0242936 Center pain C0034063 Pulmonary edema HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024525 Malacoplakia HSDN C1963064 Anxiety adverse event C1864112 Huntington disease-like 1 MalaCards|HPO C0015672 Decreased energy C0007121 Bronchogenic carcinoma HSDN C0004134 Dyssynergia C0744746 Hemiparesis ataxic UMLS C2242996 Tingling C0268450 Gitelman syndrome MalaCards|HPO C0016199 Pain flank C1336437 Stage iv renal pelvis and ureter cancer UMLS C4084768 Usual severity vomiting C1855102 Methylmalonic aciduria cblb type HPO C4084774 Have weight loss C0235461 Androgen excess HSDN C0037316 Not enough sleeping C0004941 Behavioral symptoms HSDN C4084724 Usual severity constipation C1306794 Wound botulism OrphaNet|MalaCards C0018784 Deafness sensorineural C0796133 Ramon syndrome MalaCards C0271215 Blindness legal C1834759 Momo syndrome MalaCards C1963087 Constipation adverse event C0008325 Cholecystitis HSDN C0151686 Growth retardation C0795947 Fryns-van den berghe syndrome MalaCards C1263846 Attention deficit disorder with hyperactivity C0282512 Landau-kleffner syndrome MalaCards|HPO C0030193 Sense of pain C1511305 Breast columnar cell mucinous carcinoma UMLS C0036572 Convulsion C0425045 Sudden infant death HSDN C1557397 Adverse event associated with pain C0037578 Soft tissue injury HSDN C0019079 Bloody sputum C0032788 Postoperative hemorrhage HSDN C0026838 Spasticity muscle C1963064 Anxiety adverse event HSDN C0043352 Absent salivary secretion C1306794 Wound botulism MalaCards C0036572 Convulsion C3809753 Mental retardation, autosomal recessive 38 MalaCards C0042963 Symptoms vomiting C0267204 Drug-induced nausea and vomiting, nos UMLS C3274924 Have been coughing C0262655 Recurrent urinary tract infection HSDN C1963281 Vomiting adverse event C0085293 Hepatitis e MalaCards C4084727 Cough frequency C0017181 Gastrointestinal hemorrhage HSDN C0040822 D tremors C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C2984058 Have pain C0006325 Bruxism HSDN C3829611 Nausea frequency C0011265 Presenile dementia HSDN C0848203 Male pelvic pain C0023467 Leukemia, myelocytic, acute HSDN C0011991 Loose stools C2931299 Zap70 deficiency UMLS C0002962 Angina C0026266 Mitral valve insufficiency HSDN C0427068 Legs weakness C3888271 Neuronopathy, distal hereditary motor, type iid MalaCards C0264272 Nose discharge, purulent C0339820 Cavity diseases nasal UMLS C1963090 Dehydration adverse event C0268293 Corticosterone methyl oxidase type i deficiency HPO C0424755 Fever symptoms C0009938 Bruising HSDN C4084769 Vomiting frequency C1333764 Gastric cronkhite canada polyposis MalaCards C1963091 Diarrhea adverse event C0006285 Bronchopneumonia HSDN C4084802 Usual severity diarrhea C0020732 Iatrogenic disease HSDN C0518090 Frequency of pain question C0020655 Hypothalamic diseases HSDN C0242936 Center pain C0043255 Stab wound HSDN C0038002 Spleen enlargement C1836727 Peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease HPO C0002962 Angina C0001828 Agricultural workers' diseases HSDN C4020887 Photodysphoria C1562894 Thiel-behnke corneal dystrophy MalaCards|HPO C2203646 Jaundice C0002895 Anemia, sickle cell MalaCards|HSDN|HPO C0008031 Pain chest C0342649 Vascular calcification HSDN C0030552 Paralysis partial C1970180 Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation HPO C0522224 Palsied C0013502 Echinococcosis HSDN C4084775 Usual severity weight loss C0035358 Retroperitoneal neoplasm HSDN C4084768 Usual severity vomiting C0032268 Pneumocephalus HSDN C0030554 Abnormal sensation C0035923 German measles vaccine HSDN C0237326 Defecation pain C1839333 Epileptic encephalopathy, early infantile, 2 MalaCards|HPO C0857305 Thrombocytopenia purpura C0030305 Pancreatitis HSDN C0020580 Decreased sensation C0008625 Chromosome aberrations HSDN C0036396 Sciatica C0029423 Cartilaginous exostosis HSDN C0034063 Edema lung C3531896 Fatal congenital nonlysosomal heart glycogenosis MalaCards C0413252 Hypothermia due to exposure C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4085317 Diarrhea frequency C0026650 Movement disorders HSDN C4085222 Nausea C0021799 Interprofessional relations HSDN C0013362 Dysarthrias C0751279 Metachromatic leukodystrophy, adult-type (disorder) HPO C3665346 Loss sight C1836202 Mental retardation, keratoconus, febrile seizures, and sinoatrial block UMLS C0013362 Dysarthrias C1849140 Spastic ataxia, charlevoix-saguenay type MalaCards|HPO C0013404 Respiratory difficulty C0032019 Pituitary neoplasms HSDN C0231528 Muscle pain generalized C3714933 Myopathy due to myoadenylate deaminase deficiency MalaCards C0237326 Defecation pain C0342200 Endemic cretinism MalaCards C0424755 Fever symptoms C0023381 Letterer-siwe disease MalaCards C4085548 Usual severity dizziness C2239176 Liver carcinoma HSDN C1963281 Vomiting adverse event C1000483 Genus anemia HSDN C1963252 Tremor adverse event C0751772 Rem sleep behavior disorder HSDN C0857278 Band-like headache C0033893 Tension headache UMLS C0003862 Pain joint C0018802 Congestive heart failure HSDN C0013390 Cramps menstrual C0003873 Rheumatoid arthritis HSDN C0413252 Hypothermia due to exposure C0206255 Malaria vaccine HSDN C0030193 Sense of pain C0267515 Chronic idiopathic anal pain UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0010674 Cystic fibrosis HSDN C0036572 Convulsion C1963120 Gynecomastia adverse event HSDN C0026821 Cramp C0019054 Hemolysis (disorder) HSDN C0085631 Abnormal excitement C0007873 Uterine cervical neoplasm HSDN C0023015 Language handicap C1853578 Neuroferritinopathy MalaCards|HPO C1963093 Dizziness adverse event C0015467 Neuralgia facial HSDN C0020673 Hypothermia (central) (local) C1704272 Benign prostatic hyperplasia HSDN C0013404 Respiratory difficulty C0037942 Spinal osteophytosis HSDN C3463815 Feel fatigue C1962971 Myocarditis adverse event HSDN C0031911 Pigment deposition C0079504 Hermanski-pudlak syndrome MalaCards C0009806 Constipate C3244301 Coverage level - family HSDN C0018784 Deafness sensorineural C3489796 Thyroid hormone resistance, generalized, autosomal recessive OrphaNet|HPO|MalaCards C4084776 Weight loss C0031485 Phenylketonurias HSDN C2936821 Spinal cerebrospinal fluid leak C0027809 Neurilemmoma HSDN C2024893 Cardiovascular surgery result: fatigue C3463824 Myelodysplastic syndrome HSDN C4084784 Diarrhea C0038273 Stereotypic movement disorder HSDN C0231528 Muscle pain generalized C0085652 Pyoderma gangrenosum OrphaNet|MalaCards C0015230 Exanthem C0151436 Vasculitis, leukocytoclastic, cutaneous OrphaNet|MalaCards C1963091 Diarrhea adverse event C0013377 Dysgerminoma HSDN C0035078 Failure kidney C1970479 Branchiootorenal syndrome 2 MalaCards|HPO C0232503 Bleeding umbilical C0457567 Disorder of body wall and cavities UMLS C0023530 Leukopenia C0268225 Aspartylglucosaminuria MalaCards|HPO C2984058 Have pain C0032290 Aspiration pneumonia HSDN C0042420 Vasovagal episode C0007097 Carcinomas HSDN C0151786 Weakness muscle C0038395 Streptococcal infections HSDN C2242996 Tingling C1955869 Malformations of cortical development HSDN C1963071 Back pain adverse event C2240378 Cleft palate on exam HSDN C4085661 Usual severity nausea C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0027497 Queasy C0027643 Neoplasm recurrence, local HSDN C1384666 Decreased hearing C1332140 Acrofacial dysostosis MalaCards C0851578 Disorder sleep C0752299 Sleep wake transition disorders HSDN C4084766 Vomiting C0162872 Aortic aneurysm, thoracic HSDN C4085211 Pain distress question C1456784 Paranoia HSDN C0013595 Eczematous dermatitis C1706004 Anhydrotic ectodermal dysplasias OrphaNet|MalaCards C0028081 Night sweat C0279541 Hd, nodular sclerosis, adult UMLS C0024312 Lymphocytopenia C1744558 T-lymphocyte deficiency MalaCards C0012833 Dizzy C0001721 Emotional affect HSDN C4084767 Bothered by vomiting C0043208 Wolman disease HPO C0423735 Tenesmus, urinary vesical C0810038 Genitourinary symptoms and ill-defined conditions UMLS C0042963 Symptoms vomiting C0002989 Epithelioid hemangioma of skin HSDN C3641756 Have diarrhea C0334299 Carcinoid tumor no icd-o subtype HSDN C1963137 Hydrocephalus adverse event C0702169 Acrania MalaCards C0018681 Headache, cephalalgia C0085437 Meningitis, bacterial HSDN C0030975 Disorders perception C0752322 Epilepsy, partial, sensory HSDN C0009398 Color vision defects C0011860 Diabetes mellitus, non-insulin-dependent HSDN C1384666 Decreased hearing C2930815 Acute cerebral gaucher disease MalaCards C2242996 Tingling C0042373 Vascular diseases HSDN C0027066 Myoclonic jerking C0393619 Symptomatic myoclonus UMLS C0020580 Decreased sensation C2911643 Encounter due to family history of osteoporosis HSDN C1962972 Proteinuria adverse event C0268529 Proline dehydrogenase deficiency OrphaNet|HPO|MalaCards C2096293 Ent surgical result ear vertigo C0206663 Neuroectodermal tumor, primitive MalaCards C0013421 Dystonia C0334123 Histiocytosis, lipoid MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0023530 Leukopenia HSDN C0007758 Cerebellar ataxia C0003507 Aortic valve stenosis HSDN C2024893 Cardiovascular surgery result: fatigue C0010481 Cushing syndrome OrphaNet|HSDN|HPO|MalaCards C1963087 Constipation adverse event C0032787 Postoperative complications HSDN C2984058 Have pain C0521170 Fracture due to osteoporosis HSDN C0085602 Polydypsia C4022657 Abnormal drinking behavior UMLS C0232848 Enuresis, secondary C1858392 Nephronophthisis 3 MalaCards|UMLS C4085642 Level of joint stiffness C0023522 Leukodystrophy, metachromatic OrphaNet|MalaCards C0857305 Thrombocytopenia purpura C0043251 Wounds and injuries HSDN C0007166 Cardiac output decreased C0453996 Tobacco smoking HSDN C0007758 Cerebellar ataxia C0268226 Type i mucolipidosis OrphaNet|HPO C0012569 Double vision C0027439 Nasopharyngeal neoplasms HSDN C0022346 Yellow skin C0032963 Pregnancy complications, cardiovascular HSDN C0033377 Caudal displacement C0795793 Chorioretinal dysplasia-microcephaly-mental retardation syndrome MalaCards C0151786 Weakness muscle C0278120 Spinal cord paresis, motor level UMLS C0234378 Postural tremor C0752121 Spinocerebellar ataxia type 2 MalaCards|HPO C0013404 Respiratory difficulty C0004364 Autoimmune diseases HSDN C2919142 Short stature adverse event C3468041 Fanconi anemia, complementation group c MalaCards C2203646 Jaundice C1856403 Etfb deficiencies HPO C0013604 Edematous C0030483 Paraphimosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0008088 Child psychiatry HSDN C0004941 Behavioral symptoms C2678480 Chromosome 22q11.2 deletion syndrome, distal MalaCards C0004604 Pain back C0030354 Papilloma HSDN C3641756 Have diarrhea C0273486 Cranial nerve x injury HSDN C0018772 Deafness C1834711 Cerebelloparenchymal disorder vi MalaCards|HPO C0151786 Weakness muscle C0700359 Organophosphate poisoning HSDN C4084766 Vomiting C0018944 Hematoma HSDN C0033774 Skin pruritus C1962986 Glaucoma adverse event HSDN C3539896 Pelvic pain occurs with urination C0206630 Endometrial stromal sarcoma HSDN C0015230 Exanthem C1275426 Generalised atopic dermatitis UMLS C3898969 Have been vomiting C1868649 Panic disorder 1 HSDN C4085210 Usual severity pain C0085404 Poems syndrome MalaCards|HSDN C0018681 Headache, cephalalgia C0022810 Disease, kyasanur forest MalaCards C0424755 Fever symptoms C0872315 Communicable diseases emerging HSDN C0015672 Decreased energy C1859726 Arterial tortuosity syndrome MalaCards C4084776 Weight loss C0342623 Senile systemic amyloidosis MalaCards C4085211 Pain distress question C0348018 Projections HSDN C0036572 Convulsion C0268247 Niemann-pick disease, type d MalaCards|HPO C4084727 Cough frequency C2931854 Allergic bronchopulmonary mycosis MalaCards C4084766 Vomiting C0029443 Osteomyelitis HSDN C4084773 Bothered by weight gain C0036974 Shock HSDN C0003910 Articulation disorder C0038454 Cerebrovascular accident HSDN C0013395 Indigestion C0857034 Acid dyspepsia UMLS C4084776 Weight loss C0031090 Periodontal diseases HSDN C0036572 Convulsion C1336829 Meningioma of tuberculum sellae UMLS C0008031 Pain chest C0036310 Scheuermann's disease HSDN C0019209 Large liver C3554004 Pbd13a MalaCards C2220163 Skin lesion on both sides of upper lip C0037284 Skin lesion UMLS C0413252 Hypothermia due to exposure C0016483 Food preferences HSDN C0010038 Corneal opacity disorder C0796140 Gingival fibromatosis-corneal dystrophy syndrome MalaCards C0020903 Illusion C0018467 Habituation, psychophysiologic HSDN C0043094 Weight gain C0035222 Respiratory distress syndrome, adult HSDN C0917816 Deficiency mental C4014780 Orofaciodigital syndrome xiv MalaCards C4085211 Pain distress question C0848558 Hypospadias HSDN C2984057 Have nausea C0016658 Fracture bone HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0035066 Renal artery obstruction HSDN C4084774 Have weight loss C0024668 Mammary neoplasms, experimental HSDN C4084802 Usual severity diarrhea C3668816 Inflammation of non-human mammary gland HSDN C4084773 Bothered by weight gain C0000833 Abscess HSDN C0860635 Fugue state C0020703 Hysterical fugue UMLS C3898969 Have been vomiting C1856403 Etfb deficiencies HPO C0242936 Center pain C0269185 Uterus retroverted HSDN C3641756 Have diarrhea C0041466 Typhoid fever DiseaseOntology|HSDN|MalaCards C0242936 Center pain C0034088 Pulmonary valve insufficiency HSDN C1260880 Nasal drip C1377785 Nasal cavity carcinoma UMLS C4085210 Usual severity pain C1696469 Shin splints HSDN C4084774 Have weight loss C0021361 Female infertility HSDN C4084788 Have dizziness C1962979 Burn adverse event HSDN C4049644 Depression C1861457 Progressive encephalomyelitis with rigidity MalaCards C4084768 Usual severity vomiting C0887833 Carcinoma, pancreatic ductal HSDN C0034155 Thrombotic thrombocytopenic purpura C0027765 Nervous system disorder HSDN C0028738 Nystagmus C2713347 7-dehydrocholesterol reductase deficiency MalaCards|HPO C0011991 Loose stools C0002357 Altruism HSDN C0036396 Sciatica C1546654 Specimen source codes - granuloma HSDN C1963249 Tinnitus adverse event C0751188 Dural headache post puncture HSDN C0004134 Dyssynergia C1881674 Medical device emits smoke HSDN C4085210 Usual severity pain C0041466 Typhoid fever HSDN C3274924 Have been coughing C0006288 Bronchopulmonary sequestration HSDN C1090821 Sepsis C1844376 Granulomatous disease, chronic, x-linked MalaCards C0013911 Emaciate C0011848 Diabetes insipidus HSDN C0000737 Abdomen pain C1332243 Adenocarcinoma of ampulla of vater UMLS C0424755 Fever symptoms C0039263 Takayasu arteritis OrphaNet|HSDN|HPO|MalaCards C3665347 Vision impaired C0268344 Ehlers-danlos syndrome 6b OrphaNet|HPO|MalaCards C0004134 Dyssynergia C2073625 X-ray of chest: pleural effusion HSDN C4084774 Have weight loss C0032851 Disease poultry HSDN C2911645 Weight loss adverse event C0011334 Dental caries HSDN C4085317 Diarrhea frequency C0022865 Obstetric labor complications HSDN C0004604 Pain back C0032343 Poisoning HSDN C0349588 Stature short C0038015 Spondyloepiphyseal dysplasia OrphaNet C0018991 Paralysis one side of body C0036864 Sexual relations HSDN C1963091 Diarrhea adverse event C1449843 Pseudohypoaldosteronism, type i, autosomal recessive HPO C4085549 Dizziness C0038941 Incisional infection HSDN C0030486 Extremity paralysis, lower C0007795 Diffuse cerebral sclerosis of schilder HSDN C1838869 Proximal neurogenic muscle weakness C4014605 Polyglucosan body myopathy 1 with or without immunodeficiency MalaCards C0030200 Intractable pain C0949760 Personal autonomy HSDN C0011206 Delirium acute C0344434 Atrial fibrillation ecg HSDN C0037763 Spasm C0267601 Anismus UMLS C3887638 Failure to thrive in infant C0475813 Alpha thalassemia-mental retardation syndrome OrphaNet|HPO|MalaCards C2237041 Shox gene with short stature C0155338 Total ophthalmoplegia MalaCards C0013604 Edematous C0026103 Mikulicz disease HSDN C4084767 Bothered by vomiting C0079631 Interdisciplinary communication HSDN C2919142 Short stature adverse event C0265216 X-linked hydrocephalus syndrome MalaCards C0375560 Abdominal or pelvic swelling, mass, or lump, left lower quadrant C0810319 Other and unspecified gastrointestinal disorders UMLS C0030200 Intractable pain C0010267 Cranial nerve neoplasms HSDN C0751837 Gait ataxic C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C3494358 Characteristic, prodromal C0004936 Mental disorders HSDN C3539893 Pelvic pain occurs with intercourse C0017638 Glioma HSDN C4020887 Photodysphoria C1856899 Cutaneous albinism hermine phenotype MalaCards C0030193 Sense of pain C0023493 Adult t-cell lymphoma/leukemia HSDN C3463815 Feel fatigue C0162871 Aortic aneurysm, abdominal HSDN C0000737 Abdomen pain C0029401 Osteitis deformans HSDN C0349588 Stature short C1836602 Bruck syndrome 2 OrphaNet|HPO|MalaCards C2984057 Have nausea C0002895 Anemia, sickle cell HSDN C4084773 Bothered by weight gain C0015461 Facial neoplasms HSDN C0009398 Color vision defects C0002985 Angiokeratoma HSDN C0009421 Comatose C0034530 Injury radiation HSDN C4084802 Usual severity diarrhea C0038273 Stereotypic movement disorder HSDN C3146279 Coma C0022758 Kap HSDN C1549543 Administration method - pain C0024449 Fungal mycetoma HSDN C0018784 Deafness sensorineural C1850600 Leigh syndrome due to mitochondrial complex v deficiency HPO C3887638 Failure to thrive in infant C0034341 Pyruvate carboxylase deficiency disease HSDN C2024878 Cardiovascular surgery result: dyspnea C0006109 Brain damage, chronic HSDN C0019209 Large liver C1863236 Scid due to ada deficiency, early-onset HPO C0018808 Murmur C0003499 Supravalvular aortic stenosis HSDN C1557397 Adverse event associated with pain C0016978 Gallbladder neoplasm HSDN C3887784 Decreased urine output C0080274 Urinary retention HSDN C4084768 Usual severity vomiting C1858656 Short stature, idiopathic, autosomal MalaCards C0427055 Face weakness C0410226 Congenital myotonic dystrophy MalaCards C1069915 Vertigo C0034069 Pulmonary fibrosis HSDN C0587246 Extremity weakness C1842197 Charcot-marie-tooth disease, recessive intermediate a HPO C0015468 Face pain C0011428 Dentigerous cyst HSDN C0473234 Blood in the urine associated with pain C0042075 Urologic diseases UMLS C3463815 Feel fatigue C0002438 Amebiasis HSDN C4084768 Usual severity vomiting C3150894 Chromosome 19p13.13 deletion syndrome MalaCards C0848203 Male pelvic pain C0042063 Urogenital abnormalities HSDN C0151786 Weakness muscle C1848029 Ehlers-danlos syndrome caused by tenascin-x deficiency OrphaNet C0002962 Angina C0009763 Conjunctivitis HSDN C4085211 Pain distress question C2073625 X-ray of chest: pleural effusion HSDN C1963091 Diarrhea adverse event C0600104 Obsessive compulsive behavior HSDN C0000737 Abdomen pain C0004692 Balantidiasis MalaCards C4084784 Diarrhea C0018273 Growth disorders HSDN C3541349 Syncope C0024841 Matrimony, matrimonial HSDN C4084766 Vomiting C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency HPO C1963087 Constipation adverse event C0010695 Cystocele HSDN C0036572 Convulsion C1855008 Mitochondrial complex ii deficiency MalaCards|HPO|UMLS C0015672 Decreased energy C1866552 Paragangliomas 2 (disorder) MalaCards C0242936 Center pain C0005745 Blepharoptosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041601 Ulna fracture HSDN C0015672 Decreased energy C0020651 Hypotension, orthostatic HSDN C3539891 Pelvic pain to the rear C0282606 Myomatous neoplasm HSDN C0497406 Over weight C0011615 Dermatitis, atopic HSDN C0020538 Hbp C0003490 Aortic arch syndrome MalaCards C1962972 Proteinuria adverse event C0023434 Chronic lymphocytic leukemia HSDN C3244654 Sore throat brand of benzocaine & menthol C0021400 Influenza DiseaseOntology|MalaCards C0042571 Vertigo subjective C0524851 Neurodegenerative disorders HSDN C0151786 Weakness muscle C0022660 Kidney failure, acute HSDN C0497406 Over weight C0025202 Melanoma HSDN C0042963 Symptoms vomiting C0001175 Acquired immunodeficiency syndrome HSDN|UMLS C4085210 Usual severity pain C1299919 Enteric coccidiosis HSDN C4085317 Diarrhea frequency C0036420 Localized scleroderma HSDN C0040034 Thrombocytopenia C0086438 Hypogammaglobulinemia MalaCards C0027796 Neuralgias C0002395 Alzheimer's disease HSDN C0019825 Voice hoarseness C1334666 Mediastinal malignant non-seminomatous germ cell neoplasm UMLS C4084727 Cough frequency C0162820 Dermatitis, allergic contact HSDN C0237326 Defecation pain C0796003 Juberg-marsidi syndrome HPO C3641756 Have diarrhea C0001726 Affective symptoms HSDN C0004134 Dyssynergia C0026755 Multiple carboxylase deficiency HSDN C2024893 Cardiovascular surgery result: fatigue C0007193 Cardiomyopathy, dilated HSDN C3887873 Hearing loss C0036974 Shock HSDN C0349588 Stature short C0026707 Mucopolysaccharidosis iv OrphaNet|MalaCards C2237041 Shox gene with short stature C0376524 Branchio-oculo-facial syndrome OrphaNet|HPO|MalaCards C1000483 Genus anemia C3810350 Bone marrow failure syndrome 2 MalaCards C2984058 Have pain C0032229 Pleural neoplasms HSDN C4084776 Weight loss C0018916 Hemangioma HSDN C2031027 Hip joint stiff causing difficulty crossing leg over knee C1861833 Cataract, congenital, volkmann type MalaCards C0038002 Spleen enlargement C0268532 Deficiency of prolidase MalaCards|HPO C4084726 Distress cough C0020456 Hyperglycemia HSDN C0024282 Lymphocytosis C3541994 Drug hypersensitivity syndrome OrphaNet|MalaCards C4084775 Usual severity weight loss C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C1090821 Sepsis (invertebrate) HSDN C0040822 D tremors C0220994 Hyperammonemia HSDN C0030486 Extremity paralysis, lower C0033817 Pseudomonas infections HSDN C0013404 Respiratory difficulty C0751674 Lymphangioleiomyomatosis OrphaNet|HPO|MalaCards C3665492 Pigmentations C0017638 Glioma MalaCards C0000737 Abdomen pain C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C0040485 Wryneck C0026764 Multiple myeloma HSDN C3815497 Cough C2984289 Melanoma pathway HSDN C0406405 Delayed cold sensitivity C0021368 Inflammation UMLS C0518090 Frequency of pain question C0311375 Arsenic poisoning HSDN C0018681 Headache, cephalalgia C0035288 Reticuloendotheliosis, x-linked MalaCards C0413252 Hypothermia due to exposure C0017658 Glomerulonephritis HSDN C0043094 Weight gain C0035457 Rhinitis, allergic, perennial HSDN C0036572 Convulsion C3897751 Recurrent childhood gliomatosis cerebri UMLS C0424755 Fever symptoms C0014661 Equine infectious anemia MalaCards C0015469 Facial paralysis C1834846 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 HPO C1963180 Neck pain adverse event C0020538 Hypertensive disease HSDN C0030193 Sense of pain C0032578 Polyploidy HSDN C0497406 Over weight C0001973 Alcoholic intoxication, chronic HSDN C0033774 Skin pruritus C0406238 Pruriginous atopic dermatitis UMLS C4085211 Pain distress question C0018915 Hemangioendothelioma HSDN C0426579 Anorexia symptom C1881600 Malignant vipoma MalaCards C0231218 Malaise generalized C0019097 Hemorrhagic fever, argentinian MalaCards C4084802 Usual severity diarrhea C0023487 Acute promyelocytic leukemia HSDN C0042024 Urine incontinence C0007350 Cat disease HSDN C0022346 Yellow skin C0022423 Judgement HSDN C4085210 Usual severity pain C0006384 Bundle-branch block HSDN C3539020 Pelvic pain decreasing in frequency C1546602 Specimen source codes - diverticulum HSDN C2024893 Cardiovascular surgery result: fatigue C0391817 Drug-induced autoim haem anaem OrphaNet|MalaCards C0152228 Diplacusis, unspecified ear C0375257 Auditory perception and discrimination disorders UMLS C3146279 Coma C0014059 Encephalomyelitis, acute disseminated HSDN C0034933 Abnormal reflexes C0549122 Relative afferent pupillary defect UMLS C0000737 Abdomen pain C0022350 Jaundice, chronic idiopathic MalaCards|HPO C1963071 Back pain adverse event C0007133 Carcinoma, papillary HSDN C0151827 Pain eye C0035302 Retinal artery occlusion HSDN C2008812 Frequent passing of large blood clots during periods C0025345 Menstruation disturbances UMLS C0235634 Costal margin tenderness C0009447 Common variable immunodeficiency UMLS C0850758 Pain pelvic C0009244 Behavioral cognitive therapy HSDN C4085317 Diarrhea frequency C3152144 Agammaglobulinemia 1, autosomal recessive HPO C0026838 Spasticity muscle C1548578 Location characteristic id - smoking HSDN C2984057 Have nausea C0001807 Aggressive behavior HSDN C4049602 Hyperactivity C0751748 Nonketotic hyperglycinemia MalaCards|HPO C1962972 Proteinuria adverse event C0028796 Dermatitis, occupational HSDN C0231712 Gait waddling C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0003811 Cardiac rhythm disturbance C2673677 Myopathy, early-onset, with fatal cardiomyopathy MalaCards|HPO C3887638 Failure to thrive in infant C0268124 Adenosine deaminase deficiency MalaCards C0151686 Growth retardation C0795887 Chromosome xp21 deletion syndrome MalaCards C0030486 Extremity paralysis, lower C0003507 Aortic valve stenosis HSDN C4084769 Vomiting frequency C0015726 Focused anxiety HSDN C0027796 Neuralgias C0276585 Aids with neuralgia, nos UMLS C1557397 Adverse event associated with pain C0178282 Hernia of abdominal cavity HSDN C0270327 Bed wetting C0268164 Primary hyperoxaluria, type i HPO C1069915 Vertigo C0023418 Leukemia HSDN C0034150 Skin purpura C0042974 Von willebrand disease HSDN C2911647 Weight gain adverse event C0004364 Autoimmune diseases HSDN C0557874 Global developmental delay C2931888 Pfeiffer type acrocephalosyndactyly MalaCards C4085317 Diarrhea frequency C0008626 Congenital chromosomal disease HSDN C0917816 Deficiency mental C1864852 Catshl syndrome HPO C2315100 Pediatric failure to thrive C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C0917816 Deficiency mental C2931285 Congenital testicular deficiency MalaCards C0005745 Blepharoptosis C1802395 Congenital muscular hypertrophy-cerebral syndrome MalaCards|HPO C2984057 Have nausea C0014849 Esophageal and gastric varices HSDN C1384666 Decreased hearing C0016510 Foot diseases HSDN C0042025 Urinary incontinence stress C0034065 Pulmonary embolism HSDN C2237041 Shox gene with short stature C0162671 Melas syndrome OrphaNet|HPO|MalaCards C4084766 Vomiting C0237873 Physiological sexual disorders HSDN C0020672 Body temperature decreased C0022876 Premature obstetric labor HSDN C0030552 Paralysis partial C1412058 Abca1 gene HSDN C0003550 Broca aphasia C0151744 Myocardial ischemia HSDN C0009398 Color vision defects C0026707 Mucopolysaccharidosis iv HSDN C4084766 Vomiting C0018923 Hemangiosarcoma HSDN C0023012 Delay language C0751667 Canavan disease, juvenile OrphaNet|HPO C0028738 Nystagmus C3554385 Congenital disorder of glycosylation, type iu MalaCards C0038506 Stutter C0035010 Reinforcement, verbal HSDN C2911647 Weight gain adverse event C0007177 Cardiac tamponade HSDN C4085661 Usual severity nausea C1963119 Stomach ulcer adverse event HSDN C1384666 Decreased hearing C1785148 Rapp-hodgkin syndrome HPO C0012833 Dizzy C0026764 Multiple myeloma HSDN C2029884 Hearing loss by exam C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C0011991 Loose stools C0009447 Common variable immunodeficiency HPO|UMLS C0522224 Palsied C0014556 Epilepsy, temporal lobe HSDN C4084802 Usual severity diarrhea C0221021 Microangiopathic hemolytic anemia MalaCards C0241210 Speaking delay C3280544 Mental retardation, autosomal recessive 25 MalaCards C0234979 Dysdiadochokinesia C3554605 Mc3dn2 MalaCards|UMLS C0013604 Edematous C3163843 Chondrosarcoma of bone HSDN C0004941 Behavioral symptoms C0266470 Cerebellar hypoplasia OrphaNet C4085661 Usual severity nausea C0439840 Reflex motion descriptor HSDN C0151686 Growth retardation C0678202 Granulomatous enteritis MalaCards C0027497 Queasy C0014852 Esophageal diseases UMLS C4084724 Usual severity constipation C4084909 Depression subordinate domain HSDN C0027498 Nausea vomiting C0687720 Central diabetes insipidus MalaCards C0042963 Symptoms vomiting C0001721 Emotional affect HSDN C2242996 Tingling C0001175 Acquired immunodeficiency syndrome HSDN C0009421 Comatose C0205788 Histiocytoid hemangioma HSDN C4084766 Vomiting C0035436 Rheumatic fever HSDN C1000483 Genus anemia C1861451 Stormorken syndrome OrphaNet|HPO|MalaCards C2048468 Inability to impregnate C1960539 Aromatase deficiency OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0014175 Endometriosis HSDN C0007758 Cerebellar ataxia C0020757 Ichthyoses HSDN C0030552 Paralysis partial C1096063 Drug resistant epilepsy HSDN C1443924 Severe diarrhea C0019911 Hookworm infections MalaCards C2203646 Jaundice C0028064 Niemann-pick diseases MalaCards C0085606 Urination urgency C1832669 Spastic paraplegia 9, autosomal dominant (disorder) MalaCards|HPO C0004604 Pain back C0007124 Noninfiltrating intraductal carcinoma HSDN C1549543 Administration method - pain C0005417 Bile duct fistula HSDN C4085661 Usual severity nausea C0038159 Food poisoning, staphylococcal DiseaseOntology|MalaCards C0004604 Pain back C0221013 Mastocytosis, systemic HSDN C0036572 Convulsion C0162526 Aids-related opportunistic infections HSDN C3665386 Abnormal vision C3551954 Coenzyme q10 deficiency, primary, 1 MalaCards C0036572 Convulsion C0021670 Insulinoma OrphaNet|HSDN|HPO|MalaCards C0015970 Fever unknown origin C0343525 Lemierre syndrome HSDN C0020796 Profoundly mentally retarded C3553330 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 MalaCards C1069915 Vertigo C0034088 Pulmonary valve insufficiency HSDN C0497247 Blood pressure elevation C1859727 Arterial calcification of infancy MalaCards|HPO C0917816 Deficiency mental C3280523 Mental retardation, autosomal recessive 31 MalaCards C1963093 Dizziness adverse event C0027149 Myxoma HSDN C0036572 Convulsion C0009492 Compartment syndromes HSDN C0042024 Urine incontinence C0030920 Peptic ulcer HSDN C3146279 Coma C0030920 Peptic ulcer HSDN C3641755 Have constipation C0027947 Neutropenia HSDN C1962972 Proteinuria adverse event C0034069 Pulmonary fibrosis HSDN C0040822 D tremors C0162671 Melas syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0235032 Neurotoxicity syndromes HSDN C4084802 Usual severity diarrhea C0042035 Urination disorders HSDN C0557874 Global developmental delay C2678486 Temple-baraitser syndrome MalaCards|HPO C0036396 Sciatica C0009241 Cognition disorders HSDN C0006370 Bulimia C0150277 Meditations HSDN C0030486 Extremity paralysis, lower C0003125 Anorexia nervosa HSDN C2096293 Ent surgical result ear vertigo C3539923 Cdisc adas-cog - orientation summary score HSDN C0232466 Feeding difficulty C2750785 Muscular dystrophy, congenital, lmna-related (disorder) OrphaNet|HPO C0684343 Pseudophakia C0015405 Fungal eye infections HSDN C0007758 Cerebellar ataxia C1857780 Joubert syndrome 5 MalaCards|HPO C0413252 Hypothermia due to exposure C0021843 Intestinal obstruction HSDN C3829611 Nausea frequency C0020179 Huntington disease HSDN C2096293 Ent surgical result ear vertigo C2675211 Episodic ataxia, type 6 (disorder) MalaCards C0001825 Agraphia C0001726 Affective symptoms HSDN C0232943 Metromenorrhagia C0023092 Lassa fever OrphaNet|MalaCards C0233138 Uterine incoordination - first degree C0269839 Uterine incoordination, nos UMLS C0040822 D tremors C0178842 Sensory feedback HSDN C0038868 Supranuclear palsy progressive C0020936 Imitative behaviors HSDN C4084784 Diarrhea C0021847 Intestinal pseudo-obstruction HSDN C0013404 Respiratory difficulty C0018939 Hematological disease HSDN C0221752 Rbc urine C1956258 Familial thrombotic thrombocytopenic purpura MalaCards C3641755 Have constipation C0011334 Dental caries HSDN C0013404 Respiratory difficulty C0085253 Adult-onset still disease HSDN C1963064 Anxiety adverse event C0016667 Fragile x syndrome MalaCards|HPO C0042571 Vertigo subjective C0014511 Epithelial cyst HSDN C0030193 Sense of pain C0041976 Urethritis HSDN C1145670 Failure respiratory C1801950 Opitz-g syndrome, type 2 OrphaNet|MalaCards C0018681 Headache, cephalalgia C0035078 Kidney failure HSDN C0026821 Cramp C0024299 Lymphoma HSDN C4084774 Have weight loss C0017636 Glioblastoma HSDN C0042963 Symptoms vomiting C0034065 Pulmonary embolism HSDN|UMLS C0042963 Symptoms vomiting C0023530 Leukopenia HSDN C2024893 Cardiovascular surgery result: fatigue C0040761 Transposition of great vessels HSDN C3887873 Hearing loss C0997768 Glaucoma HSDN C0032617 High urine output C0403553 Renal dysplasia and retinal aplasia (disorder) HPO|UMLS C0557874 Global developmental delay C3554209 Pontocerebellar hypoplasia, type 8 MalaCards C4050613 Anxiety C0085292 Stiff-person syndrome OrphaNet|MalaCards C0019209 Large liver C1852456 Cryoglobulinemia, familial mixed OrphaNet|MalaCards C3665347 Vision impaired C0016952 Galactosemias MalaCards C2237041 Shox gene with short stature C1851413 Exostoses, multiple, type ii HPO C0004093 Asthenia C2015799 Other disease of neurological system UMLS C3665492 Pigmentations C0027665 Neoplasms, nerve tissue MalaCards C3815497 Cough C0162429 Malnutrition HSDN C4085211 Pain distress question C0015671 Father HSDN C2203646 Jaundice C0042164 Uveitis HSDN C4084767 Bothered by vomiting C0023890 Liver cirrhosis HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0038356 Stomach neoplasms HSDN C0349588 Stature short C4014934 Imd36 MalaCards C3274924 Have been coughing C0001828 Agricultural workers' diseases HSDN C0036572 Convulsion C0022976 Animal gait disorder HSDN C0026838 Spasticity muscle C1090821 Sepsis (invertebrate) HSDN C0023380 Lethargy C0031887 Picornaviridae infections HSDN C0232462 Appetite decrease C0011993 Vipoma OrphaNet|MalaCards C0018681 Headache, cephalalgia C0018021 Goiter HSDN C4084776 Weight loss C1322286 Thymoma, type c MalaCards C0349588 Stature short C0022441 Juvenile osteochondrosis of hip MalaCards C0221166 Paraparesis C0037231 Sjogren-larsson syndrome HSDN C1549543 Administration method - pain C0020507 Hyperplasia HSDN C4084788 Have dizziness C0013364 Dysautonomia, familial HSDN C0522224 Palsied C0013595 Eczema HSDN C0010200 Cough symptom C0014461 Granuloma eosinophilic MalaCards C1963093 Dizziness adverse event C0149514 Bronchitis acute HSDN C2911647 Weight gain adverse event C0009244 Behavioral cognitive therapy HSDN C0019209 Large liver C4048705 Hypermethioninemia MalaCards C0750394 Wbc low C1855116 Methylmalonic aciduria, mut(-) type HPO C4084784 Diarrhea C0025958 Microcephaly HSDN C0027796 Neuralgias C0012691 Dislocations HSDN C4084802 Usual severity diarrhea C0009440 Common bile duct diseases HSDN C0009806 Constipate C0085655 Polymyositis OrphaNet|MalaCards C0042798 Vision dim C0020582 Hyphema of iris and ciliary body HSDN C4084725 Usual severity cough C0027746 Nerve degeneration HSDN C0030552 Paralysis partial C0017409 Herpes zoster oticus HSDN C0002962 Angina C0001807 Aggressive behavior HSDN C0020538 Hbp C1865267 Arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly OrphaNet|HPO C3829611 Nausea frequency C0021359 Infertility HSDN C0857305 Thrombocytopenia purpura C1704272 Benign prostatic hyperplasia HSDN C2024878 Cardiovascular surgery result: dyspnea C0034155 Purpura, thrombotic thrombocytopenic OrphaNet|MalaCards C2911647 Weight gain adverse event C0009241 Cognition disorders HSDN C0497406 Over weight C0023467 Leukemia, myelocytic, acute HSDN C0040485 Wryneck C0344479 Spinal cord myelodysplasia HSDN C0150055 Pain chronic C1261473 Sarcoma HSDN C3541349 Syncope C0020461 Hyperkalemia HSDN C0518090 Frequency of pain question C0022672 Acute kidney tubular necrosis HSDN C0020672 Body temperature decreased C0003850 Arteriosclerosis HSDN C0013604 Edematous C1963266 Uveitis adverse event HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0031069 Familial mediterranean fever OrphaNet|HPO C3274924 Have been coughing C0152264 Familial erythrocytosis HPO C0242936 Center pain C0684337 Ewings sarcoma-primitive neuroectodermal tumor (pnet) HSDN C0518090 Frequency of pain question C0022568 Keratitis HSDN C0037316 Not enough sleeping C0021228 Variability of individual responses HSDN C0151827 Pain eye C0524801 Retinal neoplasms HSDN C2024878 Cardiovascular surgery result: dyspnea C0018798 Congenital heart defects HSDN C0013604 Edematous C0032269 Pneumococcal infections HSDN C0024032 Birth weight subnormal C1837475 Insulin-like growth factor i deficiency OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C2711266 Infection by anisakis larva HSDN C0022346 Yellow skin C0030521 Parathyroid neoplasms HSDN C1579931 Depressed - symptom C0162531 Hereditary coproporphyria OrphaNet|HPO C4085317 Diarrhea frequency C0238198 Gastrointestinal stromal tumors HSDN C0022346 Yellow skin C0018674 Head trauma HSDN C0232466 Feeding difficulty C1291230 3-hydroxyacyl-coa dehydrogenase deficiency MalaCards C4085548 Usual severity dizziness C2984291 Glioblastoma multiforme pathway HSDN C1963086 Confusion adverse event C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0037763 Spasm C0018565 Acquired deformity of hand, nos HSDN C0003862 Pain joint C0013720 Ehlers-danlos syndrome HSDN C0033774 Skin pruritus C2987141 Pancreatic poorly differentiated ductal adenocarcinoma UMLS C0424755 Fever symptoms C0023443 Hairy cell leukemia HSDN C0241210 Speaking delay C3809877 Schaaf-yang syndrome MalaCards C4084784 Diarrhea C0004610 Bacteremia HSDN C0015672 Decreased energy C1858664 Hemochromatosis, type 3 MalaCards C0518090 Frequency of pain question C0015671 Father HSDN C2242996 Tingling C0023890 Liver cirrhosis HSDN C0026838 Spasticity muscle C1969796 Ataxia, spastic, 2, autosomal recessive (disorder) MalaCards|HPO C4084776 Weight loss C0032580 Adenomatous polyposis coli HSDN C2911645 Weight loss adverse event C0022373 Disease, jejunal HSDN C3641755 Have constipation C0018378 Guillain-barre syndrome HSDN C0042798 Vision dim C1852267 Optic atrophy 1 and deafness HPO C0018777 Deafness, conductive C1844862 Abruzzo erickson syndrome MalaCards|HPO C0242936 Center pain C0334533 Arteriovenous hemangioma HSDN C0013395 Indigestion C1522133 High cholesterol level HSDN C2242996 Tingling C0016542 Foreign body HSDN C3887638 Failure to thrive in infant C1850598 Leigh syndrome due to mitochondrial complex iii deficiency HPO C4085211 Pain distress question C0009495 Behavior, competitive HSDN C1384666 Decreased hearing C1145628 Autonomic nervous system disorders HSDN C0020903 Illusion C0006118 Brain neoplasms HSDN C0021359 Infertility C0242343 Panhypopituitarism OrphaNet|HPO|MalaCards C0017672 Pain tongue C0016053 Fibromyalgia HSDN C1963063 Anorexia adverse event C3273116 Gallbladder net MalaCards C4084774 Have weight loss C0001486 Adenovirus infections HSDN C0024031 Back pain lower back C1546602 Specimen source codes - diverticulum HSDN C4085642 Level of joint stiffness C0014084 Enchondromatosis OrphaNet|HPO|MalaCards C1962972 Proteinuria adverse event C0024525 Malacoplakia MalaCards C0036572 Convulsion C0752235 Lyme neuroborreliosis HSDN C0424755 Fever symptoms C0014714 Ergotism HSDN C0917816 Deficiency mental C3810212 Joubert syndrome 21 MalaCards C0030552 Paralysis partial C0242966 Systemic inflammatory response syndrome HSDN C4084725 Usual severity cough C3540844 Ciliary dyskinesia, primary, 20 MalaCards C2024893 Cardiovascular surgery result: fatigue C0027746 Nerve degeneration HSDN C0027497 Queasy C0021783 Internal external locus of control HSDN C4085317 Diarrhea frequency C0038579 Substance abuse, intravenous HSDN C1962972 Proteinuria adverse event C0027686 Pathologic neovascularization HSDN C4084776 Weight loss C0014836 Escherichia coli infections HSDN C0018681 Headache, cephalalgia C0013720 Ehlers-danlos syndrome HSDN C0011991 Loose stools C0268525 5-oxoprolinase deficiency MalaCards|HPO|UMLS C0031315 Phantom limb pain C0021818 Intervertebral disk displacement HSDN C0684343 Pseudophakia C0015397 Disorder of eye HSDN C0002962 Angina C0039145 Syringomyelia and syringobulbia HSDN C0010038 Corneal opacity disorder C0027832 Neurofibromatosis 2 HPO C4084784 Diarrhea C0013080 Down syndrome HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0023676 Life style HSDN C0518090 Frequency of pain question C0042961 Intestinal volvulus HSDN C0042928 Paralysis vocal cord C0019360 Herpes zoster disease HSDN C0020578 Hyperventilate C0038160 Staphylococcal infections HSDN C0042024 Urine incontinence C0032460 Polycystic ovary syndrome HSDN C0086565 Liver function abnormal C1847720 Glycine n-methyltransferase deficiency MalaCards|HPO C0241137 Skin pallor C1261287 Stenosis HSDN C0011991 Loose stools C0022423 Judgement HSDN C2911645 Weight loss adverse event C0021280 Infant nutrition disorder HSDN C0024031 Back pain lower back C0020544 Renal hypertension HSDN C0019209 Large liver C0086650 Mps iii d HPO C1963087 Constipation adverse event C0042373 Vascular diseases HSDN C0424755 Fever symptoms C0020488 Hypernatremia HSDN C0375558 Abdominal or pelvic swelling, mass, or lump, left upper quadrant C0810319 Other and unspecified gastrointestinal disorders UMLS C0018991 Paralysis one side of body C0016658 Fracture bone HSDN C0042024 Urine incontinence C0021308 Infarction HSDN C0221166 Paraparesis C0333596 Deposition of iron HSDN C0015938 Fetal macrosomia C0152232 Decapitation HSDN C1557397 Adverse event associated with pain C0085078 Lysosomal storage diseases HSDN C4084767 Bothered by vomiting C0020445 Hypercholesterolemia, familial HSDN C0018524 Hallucinate C0024530 Malaria HSDN C0033774 Skin pruritus C4084909 Depression subordinate domain HSDN C0848203 Male pelvic pain C0022410 Joint instability HSDN C0026821 Cramp C0007453 Cattle disease HSDN C0349588 Stature short C1860787 Down syndrome critical region HPO C4049644 Depression C3665349 Secondary hypothyroidism OrphaNet C0150045 Urinary incontinence urge C0042029 Urinary tract infection HSDN C4084776 Weight loss C0869332 Of water deprivation HSDN C0010200 Cough symptom C0005967 Bone neoplasms HSDN C1963086 Confusion adverse event C0038395 Streptococcal infections HSDN C0000737 Abdomen pain C0342793 Malonic aciduria MalaCards|HPO|UMLS C2911647 Weight gain adverse event C0018995 Hemochromatosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0002351 Altitude sickness HSDN C0151786 Weakness muscle C0027726 Nephrotic syndrome HSDN C1963087 Constipation adverse event C0024523 Malabsorption syndrome HSDN C4084775 Usual severity weight loss C0027947 Neutropenia HSDN C0032617 High urine output C3151482 Hypercalciuria, childhood, self-limiting HPO C4084724 Usual severity constipation C0344315 Depressed mood HSDN C2984057 Have nausea C0042345 Varicosity HSDN C0042571 Vertigo subjective C0041327 Tuberculosis, pulmonary HSDN C2315100 Pediatric failure to thrive C0079154 Congenital nonbullous ichthyosiform erythroderma OrphaNet|HSDN|HPO|MalaCards C0022346 Yellow skin C0027746 Nerve degeneration HSDN C4084767 Bothered by vomiting C0022423 Judgement HSDN C0085632 Listlessness C3888102 Frontotemporal dementia with motor neuron disease MalaCards C0013404 Respiratory difficulty C0011884 Diabetic retinopathy HSDN C0038868 Supranuclear palsy progressive C0333641 Atrophic HSDN C0034150 Skin purpura C0032131 Plasmacytoma HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0025290 Aseptic meningitis HSDN C0162834 Hyperpigmentation C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C2029884 Hearing loss by exam C1269683 Major depressive disorder HSDN C2203646 Jaundice C0020579 Hypervitaminosis a HSDN C0242936 Center pain C0023896 Alcoholic liver diseases HSDN C0011991 Loose stools C0025290 Aseptic meningitis HSDN C4084802 Usual severity diarrhea C1623041 Breast-fed HSDN C1963086 Confusion adverse event C0860603 Anxiety symptoms HSDN C0036572 Convulsion C0016057 Fibrosarcoma HSDN C4084768 Usual severity vomiting C1962979 Burn adverse event HSDN C0349588 Stature short C0475813 Alpha thalassemia-mental retardation syndrome OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0024299 Lymphoma HSDN C0035232 Diaphragmatic paralysis C0004044 Asphyxia HSDN C0000737 Abdomen pain C0398368 Lymphatic abnormalities HSDN C0241165 Skin thickening C0023795 Lipoid proteinosis of urbach and wiethe OrphaNet C0009806 Constipate C1864996 Enteric neuropathy, familial MalaCards C1963184 Nystagmus adverse event C0795947 Fryns-van den berghe syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0021295 Infant, premature, diseases HSDN C0344315 Mood depressed C1847987 Huntington disease-like 2 MalaCards|HPO C4084766 Vomiting C0021400 Influenza HSDN C4085210 Usual severity pain C0025297 Viral meningitis HSDN C0002962 Angina C1546847 Entity name part type - family HSDN C0015672 Decreased energy C0014175 Endometriosis HSDN C1963091 Diarrhea adverse event C0042035 Urination disorders HSDN C0013362 Dysarthrias C2674766 Myokymia 1 HPO C1963091 Diarrhea adverse event C0023886 Liver abscess, amebic HSDN C3539891 Pelvic pain to the rear C1546847 Entity name part type - family HSDN C0242936 Center pain C0043048 Experimental water deprivation HSDN C0000727 Abdomen acute C0026683 Mucocele HSDN C0018681 Headache, cephalalgia C0015695 Fatty liver HSDN C0242936 Center pain C3245466 Observationvalue - trust HSDN C0000727 Abdomen acute C0025202 Melanoma HSDN C0019209 Large liver C0268193 Nadh cytochrome b5 reductase deficiency MalaCards C0270948 Neurogenic muscular atrophy C3542021 Duchenne and becker muscular dystrophy OrphaNet|MalaCards C1962957 Flushing adverse event C0020538 Hypertensive disease HSDN C0020580 Decreased sensation C0020538 Hypertensive disease HSDN C2237041 Shox gene with short stature C2748571 Isolated growth hormone deficiency, type ib HPO C0424755 Fever symptoms C0028242 Nocardia infections HSDN C1549543 Administration method - pain C1258104 Diffuse scleroderma HSDN C0034150 Skin purpura C0023443 Hairy cell leukemia HSDN C4084727 Cough frequency C0997768 Glaucoma HSDN C0231218 Malaise generalized C2981624 Stage i intrahepatic cholangiocarcinoma UMLS C3714552 Strength decreased C1865614 Hemochromatosis, type 2a MalaCards C4085211 Pain distress question C0026683 Mucocele HSDN C2029884 Hearing loss by exam C0027658 Neoplasms, germ cell and embryonal HSDN C1963093 Dizziness adverse event C1762616 Meningioma, benign, no icd-o subtype HSDN C0151786 Weakness muscle C0003873 Rheumatoid arthritis HSDN C2984057 Have nausea C1970820 Fabry disease, cardiac variant HPO C0043094 Weight gain C0035455 Rhinitis HSDN C0151786 Weakness muscle C0206727 Nerve sheath tumors HSDN C0013132 Drooling C2678415 Hyperphenylalaninemia, bh4-deficient, due to partial pts deficiency HPO C0042963 Symptoms vomiting C0026764 Multiple myeloma HSDN C0025287 Meningitis-like C0019357 Keratitis, herpetic HSDN C2237041 Shox gene with short stature C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0518090 Frequency of pain question C0029376 Osgood schlatter disease HSDN C1838869 Proximal neurogenic muscle weakness C1853136 Neutral lipid storage disease with myopathy MalaCards|HPO C0000737 Abdomen pain C0039240 Supraventricular tachycardia HSDN C0023380 Lethargy C0684337 Ewings sarcoma-primitive neuroectodermal tumor (pnet) HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0085433 Acquired joint deformities HSDN C1565249 Limitation, mobility C0025202 Melanoma HSDN C1963170 Hypothermia adverse event C0005974 Bone resorption HSDN C0022346 Yellow skin C0019188 Hepatitis, animal HSDN C0151740 Intracranial hypertension C0221356 Brachycephaly OrphaNet|HPO|MalaCards C4085211 Pain distress question C0002170 Alopecia HSDN C3641756 Have diarrhea C2749602 Autoimmune polyendocrinopathy syndrome, type i, with reversible metaphyseal dysplasia HPO C2024878 Cardiovascular surgery result: dyspnea C0033968 Psychotherapeutic technique HSDN C0011991 Loose stools C0014852 Esophageal diseases HSDN C0043094 Weight gain C0002895 Anemia, sickle cell HSDN C0850758 Pain pelvic C0520676 Premenstrual dysphoric disorder HSDN C0427055 Face weakness C1853198 Cold-induced sweating syndrome 2 HPO C4084774 Have weight loss C0016057 Fibrosarcoma HSDN C1313952 Periodic breathing C4237041 Central sleep apnea, cheyne-stokes breathing UMLS C0033774 Skin pruritus C0036117 Salmonella infections HSDN C2032396 Pelvic pain on the right C0600041 Infective cystitis HSDN C0518090 Frequency of pain question C0006736 Body stone HSDN C0004134 Dyssynergia C1299262 Sarcoma - category (morphologic abnormality) HSDN C0039070 Collapse fleeting C0008350 Cholelithiasis HSDN C0221166 Paraparesis C0085388 Intracranial tuberculoma HSDN C4084767 Bothered by vomiting C0007820 Cerebrovascular disorders HSDN C0030794 Pelvis pain C0438692 Vaginal discharge symptom HSDN C0017565 Gingiva hemorrhage C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C0028738 Nystagmus C0023806 Lipomucopolysaccharidosis OrphaNet|HPO C0010200 Cough symptom C1334455 Pulmonary sclerosing hemangioma UMLS C3815497 Cough C0034885 Rectal neoplasms HSDN C0349588 Stature short C0044707 11 beta hsd HPO C4084774 Have weight loss C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C1963087 Constipation adverse event C0023892 Biliary cirrhosis HSDN C4084774 Have weight loss C2931876 Hirschsprung disease 1 MalaCards C0151827 Pain eye C0039841 Thiamine deficiency HSDN C0042571 Vertigo subjective C0026640 Mouth neoplasms HSDN C0043094 Weight gain C0852795 Increased insulin level HSDN C0042963 Symptoms vomiting C0024692 Mandible fracture HSDN C0030193 Sense of pain C0019050 Hemoglobinuria, paroxysmal HSDN C1963184 Nystagmus adverse event C0796085 Nance-horan syndrome OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C0019825 Voice hoarseness C0009404 Colorectal neoplasms HSDN C0042928 Paralysis vocal cord C0018022 Endemic goiter HSDN C0085593 Chill C0339959 Pneumonia chlamydial MalaCards C0019572 Hairiness C0432209 Dyssegmental dysplasia, rolland-desbuquois type MalaCards C0750394 Wbc low C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0003862 Pain joint C0033054 Prenatal exposure delayed effects HSDN C4084775 Usual severity weight loss C0027126 Myotonic dystrophy HSDN C0018772 Deafness C0853240 Mobius ii syndrome MalaCards|HPO C0522224 Palsied C0021361 Female infertility HSDN C4085210 Usual severity pain C0035328 Retinal vein occlusion HSDN C0242936 Center pain C0024143 Lupus nephritis HSDN C0518090 Frequency of pain question C0011119 Decompression sickness HSDN C1971624 Appetite absent C0043397 Yellow fever, jungle MalaCards C0018834 Brash C0867389 Chronic graft-versus-host disease MalaCards C0497406 Over weight C0026640 Mouth neoplasms HSDN C0031911 Pigment deposition C0266526 Norrie disease MalaCards C0085631 Abnormal excitement C0008073 Developmental disabilities HSDN C0151827 Pain eye C0022079 Iris neoplasms HSDN C0231528 Muscle pain generalized C0431406 Asymmetric crying face association OrphaNet|HPO C0036572 Convulsion C0013712 Ego HSDN C4085661 Usual severity nausea C0006109 Brain damage, chronic HSDN C0023015 Language handicap C1838313 Pick complex HPO C0007398 Catatonic C0040774 Transvestic fetishism or transvestism HSDN C0497247 Blood pressure elevation C1859569 Bardet-biedl syndrome 11 HPO C0026884 Muteness C0282513 Primary progressive aphasia (disorder) HPO C4085222 Nausea C0220847 C hepatitis virus HSDN C4084784 Diarrhea C0004144 Atelectasis HSDN C4084775 Usual severity weight loss C0029443 Osteomyelitis HSDN C0005904 Alteration in body temperature C0265235 Marshall syndrome MalaCards C4085210 Usual severity pain C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C3665347 Vision impaired C0346388 Malignant melanoma of choroid OrphaNet|HPO C2237041 Shox gene with short stature C0085132 Mucopolysaccharidosis vii HPO C1549543 Administration method - pain C0867389 Chronic graft-versus-host disease MalaCards C0234146 Absent reflex C0393818 Congenital hypomyelinating neuropathy HPO C0151786 Weakness muscle C0015695 Fatty liver HSDN C0030193 Sense of pain C0024198 Lyme disease HSDN C0032617 High urine output C0002064 Alkalosis, respiratory HSDN C4085222 Nausea C3163620 Hypotension adverse event HSDN C0030552 Paralysis partial C0006035 Borrelia infections MalaCards C4085548 Usual severity dizziness C0004935 Animal ethology HSDN C0029163 Hemorrhage mouth C0149745 Oral ulcer HSDN C0018524 Hallucinate C0026598 Movement perception HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0034069 Pulmonary fibrosis HSDN C0013604 Edematous C0015625 Fanconi anemia HSDN C1963137 Hydrocephalus adverse event C1844006 Hydrocephalus, x-linked, with congenital idiopathic intestinal pseudoobstruction HPO C0413252 Hypothermia due to exposure C0007117 Basal cell carcinoma HSDN C4085210 Usual severity pain C0019372 Herpesviridae infections HSDN C0413252 Hypothermia due to exposure C0020179 Huntington disease HSDN C3854600 Eyelid dystonia C0005747 Blepharospasm UMLS C0012833 Dizzy C0039231 Tachycardia HSDN C1961131 Cough adverse event C0149721 Left ventricular hypertrophy HSDN C0015300 Ocular proptosis C0265235 Marshall syndrome OrphaNet|HPO|MalaCards C0878773 Bladder hyperactive C1145628 Autonomic nervous system disorders HSDN C4084767 Bothered by vomiting C0042140 Uterine prolapse HSDN C0023012 Delay language C1859566 Bardet-biedl syndrome 8 HPO C1069915 Vertigo C1565489 Renal insufficiency HSDN C0426579 Anorexia symptom C0023240 Legionellosis MalaCards C1963184 Nystagmus adverse event C1850343 Mosaic variegated aneuploidy syndrome MalaCards|HPO C1557397 Adverse event associated with pain C1868649 Panic disorder 1 HSDN C0312416 Morning sickness C1691215 Penile hypospadias HSDN C2032483 Thigh pain radiates down leg subsides when walking stops C0079770 Lymphoma, small noncleaved-cell MalaCards C0003113 Anomia C0038263 Stereognoses HSDN C4042891 Sleep wake disorders C0014859 Esophageal neoplasms HSDN C1557397 Adverse event associated with pain C0032463 Polycythemia vera HSDN C4084775 Usual severity weight loss C0040136 Thyroid neoplasm HSDN C4085317 Diarrhea frequency C0270327 Bedwetting HSDN C0023012 Delay language C1845861 Mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait HPO C0234428 Consciousness disturbance C0751664 Canavan disease, neonatal MalaCards C0004134 Dyssynergia C0020473 Hyperlipidemia HSDN C2881386 Visual discomfort, right eye C0015397 Disorder of eye UMLS C0518090 Frequency of pain question C0043251 Wounds and injuries HSDN C0024032 Birth weight subnormal C3281152 Chromosome 16q22 deletion syndrome MalaCards C0038002 Spleen enlargement C1384600 Systemic onset juvenile chronic arthritis MalaCards|HPO C0011991 Loose stools C0042140 Uterine prolapse HSDN C4085661 Usual severity nausea C0031511 Pheochromocytoma MalaCards C2096293 Ent surgical result ear vertigo C0002395 Alzheimer's disease HSDN C0009806 Constipate C0024141 Lupus erythematosus, systemic HSDN C0038990 Sweats C1721006 Keratoderma, palmoplantar, epidermolytic OrphaNet|HPO|MalaCards C0028259 Nodule C1840560 Hidradenitis suppurativa, familial MalaCards C0041834 Erythematous condition C3280856 Ichthyosis, spastic quadriplegia, and mental retardation MalaCards C4085211 Pain distress question C0043202 Wolff-parkinson-white syndrome HSDN C0020672 Body temperature decreased C0019348 Herpes simplex infections HSDN C2315100 Pediatric failure to thrive C2674949 Chromosome 3q29 deletion syndrome MalaCards C0349588 Stature short C1857550 11-beta-hydroxysteroid dehydrogenase, type ii HPO C2096293 Ent surgical result ear vertigo C0270639 Lateral sinus thrombosis HSDN C4084768 Usual severity vomiting C0032460 Polycystic ovary syndrome HSDN C0010200 Cough symptom C0032298 Lipid pneumonia HSDN C0042940 Disorder of voice C0152180 Accessory nerve diseases HSDN C0242936 Center pain C0023827 Liposarcoma HSDN C4084774 Have weight loss C0242383 Age related macular degeneration HSDN C4084774 Have weight loss C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C4085862 Bothered by nausea C0034063 Pulmonary edema HSDN C0027498 Nausea vomiting C0019562 Von hippel-lindau syndrome OrphaNet|HPO|MalaCards C1963071 Back pain adverse event C1546602 Specimen source codes - diverticulum HSDN C0013404 Respiratory difficulty C1090821 Sepsis (invertebrate) HSDN C0036572 Convulsion C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C0557874 Global developmental delay C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0015672 Decreased energy C0012644 Animal disease models HSDN C0518090 Frequency of pain question C0016995 Gambling HSDN C0019572 Hairiness C0032249 Plummer vinson syndrome MalaCards C0004604 Pain back C2931038 Pancreatic carcinoma, familial MalaCards C0234132 Pyramidal sign C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C0000786 Abortion spontaneous C0678213 Complete hydatidiform mole MalaCards C4084766 Vomiting C0021818 Intervertebral disk displacement HSDN C3539890 Pelvic pain causes awakening at night C0206680 Mesothelioma, cystic HSDN C0027796 Neuralgias C0340629 Aortic aneurysm without mention of rupture nos HSDN C1279888 Proteinuria of undiagnosed cause C0027658 Neoplasms, germ cell and embryonal HSDN C4042891 Sleep wake disorders C0011875 Diabetic angiopathies HSDN C0010200 Cough symptom C0348018 Projections HSDN C0028738 Nystagmus C3553538 Brown-vialetto-van laere syndrome 2 MalaCards C1963071 Back pain adverse event C0007194 Hypertrophic cardiomyopathy HSDN C0749872 Upper respiratory infection symptom C0740767 Resp_tract problem UMLS C0014724 Burping C0036946 Sheep--diseases HSDN C0917816 Deficiency mental C4049701 Nephrotic syndrome - frequently relapsing MalaCards C2315100 Pediatric failure to thrive C0005956 Bone marrow diseases HSDN C0242936 Center pain C0010276 Craniopharyngioma HSDN C0086565 Liver function abnormal C0268193 Nadh cytochrome b5 reductase deficiency MalaCards C0020538 Hbp C1857556 Hsd11b2, arg208his HPO C3539022 Pelvic pain decreasing in severity C1961100 Erectile dysfunction adverse event HSDN C0027796 Neuralgias C3538785 Nci ctep sdc mesothelioma sub-category terminology HSDN C4084788 Have dizziness C0021655 Insulin resistance HSDN C0241210 Speaking delay C0220704 Shprintzen syndrome MalaCards C0034151 Hyperglobulinemic purpura C0023890 Liver cirrhosis HSDN C4084802 Usual severity diarrhea C0042018 Urinary calculi HSDN C0038990 Sweats C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C1279888 Proteinuria of undiagnosed cause C0027059 Myocarditis HSDN C4042891 Sleep wake disorders C0004377 Automatism HSDN C0002962 Angina C0026764 Multiple myeloma HSDN C0036572 Convulsion C0018571 Hand injury HSDN C1557397 Adverse event associated with pain C0151436 Vasculitis, leukocytoclastic, cutaneous HSDN C0034933 Abnormal reflexes C0009946 Conversion disorder HSDN C1971624 Appetite absent C0242952 Behavior infants HSDN C4084774 Have weight loss C0041324 Tuberculosis, osteoarticular HSDN C0015469 Facial paralysis C0011854 Diabetes mellitus, insulin-dependent HSDN C0007859 Pain neck C0005491 Biofeedback HSDN C3146279 Coma C0022665 Kidney neoplasm HSDN C4084726 Distress cough C0014236 Endophthalmitis HSDN C0011206 Delirium acute C0024121 Lung neoplasms HSDN C1384666 Decreased hearing C0037313 Sleep HSDN C0848203 Male pelvic pain C0242669 Placenta retained HSDN C4084768 Usual severity vomiting C0006309 Brucellosis HSDN C0022346 Yellow skin C0162871 Aortic aneurysm, abdominal HSDN C0700078 Deep tendon reflex decrease C1843891 Spinocerebellar ataxia 21 HPO C1069915 Vertigo C0010823 Cytomegalovirus infections HSDN C0026826 High muscle tone C1833691 Otofaciocervical syndrome OrphaNet|HPO C4084727 Cough frequency C0019655 Histoplasmosis HSDN C2984057 Have nausea C0085293 Hepatitis e MalaCards C4084776 Weight loss C0024198 Lyme disease HSDN C0559753 Daytime enuresis C0042024 Urinary incontinence UMLS C0042024 Urine incontinence C0011860 Diabetes mellitus, non-insulin-dependent HSDN C4084727 Cough frequency C0152264 Familial erythrocytosis HPO C0035078 Failure kidney C1956391 Temporal arteritis MalaCards|HPO C0027497 Queasy C0010054 Coronary arteriosclerosis HSDN C0009421 Comatose C0026961 Mydriasis HSDN C1963093 Dizziness adverse event C3541306 Plasmodium measurement HSDN C0027066 Myoclonic jerking C0033054 Prenatal exposure delayed effects HSDN C0917816 Deficiency mental C0796086 Cerebral palsy-hypotonic seizures-megalcornea syndrome OrphaNet|MalaCards C0231791 In toe C0010314 Cri-du-chat syndrome MalaCards C4084776 Weight loss C0751919 Acquired neuromyotonia OrphaNet|MalaCards C4085317 Diarrhea frequency C0025472 Mesenteric vascular occlusion HSDN C4084773 Bothered by weight gain C0040427 Tooth abnormalities HSDN C0002624 Amnesia retrograde C0038220 Status epilepticus HSDN C2096293 Ent surgical result ear vertigo C0037369 Smoking HSDN C1962972 Proteinuria adverse event C0007194 Hypertrophic cardiomyopathy HSDN C3887638 Failure to thrive in infant C0220754 Biotinidase deficiency HSDN C0019079 Bloody sputum C0004096 Asthma HSDN C0042571 Vertigo subjective C0034530 Injury radiation HSDN C0036659 Sensation disorder C0026976 Myelitis, transverse HSDN C0497247 Blood pressure elevation C0001622 Adrenal gland hyperfunction OrphaNet C0850758 Pain pelvic C0024141 Lupus erythematosus, systemic HSDN C0270327 Bed wetting C1997362 Non-neurogenic neurogenic bladder MalaCards C0030554 Abnormal sensation C0039483 Giant cell arteritis MalaCards|HPO C2926613 Chest pain:finding:point in time:^patient:ordinal C0023241 Legionnaires' disease OrphaNet|MalaCards C2911645 Weight loss adverse event C0854359 Autoimmune endocrine disease insulin syndrome OrphaNet|MalaCards C2233628 Red eyelid growth C0015424 Eyelid neoplasms UMLS C0018991 Paralysis one side of body C0040136 Thyroid neoplasm HSDN C4042891 Sleep wake disorders C1527429 Increased blood npn HSDN C1549543 Administration method - pain C0038987 Sweat gland neoplasms HSDN C0018991 Paralysis one side of body C1579931 Depressed - symptom HSDN C2242996 Tingling C1556682 Adverse event associated with infection HSDN C0344434 Atrial fibrillation ecg C3250443 Myotonic dystrophy 1 MalaCards C0018681 Headache, cephalalgia C0027059 Myocarditis HSDN C4084776 Weight loss C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C0751837 Gait ataxic C3281223 Canvas UMLS C0004604 Pain back C0004361 Autogenic therapy HSDN C0018681 Headache, cephalalgia C0393746 Headache low pressure UMLS C4042891 Sleep wake disorders C0023051 Laryngeal diseases HSDN C2242996 Tingling C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0231341 Aging premature C0020534 Orbital separation excessive HSDN C0004134 Dyssynergia C1568249 Usher syndrome, type ii MalaCards|HPO C0242936 Center pain C0040137 Thyroid nodule HSDN C0020505 Excessive eating C0032019 Pituitary neoplasms HSDN C4084776 Weight loss C0162703 Pain sensitivity HSDN C0009676 Confusion state C1552262 Nurse practitioner - family HSDN C3829611 Nausea frequency C0003507 Aortic valve stenosis HSDN C0028738 Nystagmus C0796205 Spinocerebellar ataxia, x-linked 1 MalaCards C0020458 Hyperhydrosis C1853198 Cold-induced sweating syndrome 2 HPO C0577567 Mass of urogenital structure C0154106 Uncert. neopl. genitourinary UMLS C0009763 Conjunctiva inflammation C0265345 Lymphedema distichiasis syndrome OrphaNet|HPO|MalaCards C0018784 Deafness sensorineural C0020443 Hypercholesterolemia HSDN C4084774 Have weight loss C0022865 Obstetric labor complications HSDN C0018926 Emesis bloody C0008519 Ectopic tissue HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1610547 Production class code - pleasure HSDN C4084766 Vomiting C0032266 Emphysema, intestinal HSDN C4084725 Usual severity cough C1546847 Entity name part type - family HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0020676 Hypothyroidism HSDN C4084766 Vomiting C0028738 Nystagmus HSDN C0742862 Cough with micturition C0740767 Resp_tract problem UMLS C0002622 Amnesias C0016989 Galvanic skin response HSDN C0424755 Fever symptoms C0206171 Community acquired infections HSDN C3665347 Vision impaired C3808964 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 MalaCards C3641756 Have diarrhea C0035358 Retroperitoneal neoplasm HSDN C0030486 Extremity paralysis, lower C0597109 Nurse's role HSDN C0003811 Cardiac rhythm disturbance C0917796 Optic atrophy, hereditary, leber HPO C0034642 Chest crepitation C1800706 Idiopathic pulmonary fibrosis MalaCards C2096293 Ent surgical result ear vertigo C0206255 Malaria vaccine HSDN C0019521 Hiccoughs C0001327 Laryngitis acute HSDN C0009398 Color vision defects C0026764 Multiple myeloma HSDN C0518090 Frequency of pain question C0035078 Kidney failure HSDN C0851578 Disorder sleep C0007786 Brain ischemia HSDN C2984058 Have pain C0020545 Hypertension, renovascular HSDN C4085211 Pain distress question C0003723 Arbovirus infections HSDN C0036572 Convulsion C0002871 Anemia HSDN|UMLS C0018784 Deafness sensorineural C0037744 Perceptual spatial orientation HSDN C0557874 Global developmental delay C4015344 Peroxisomal fatty acyl-coa reductase 1 disorder MalaCards C0030193 Sense of pain C0018995 Hemochromatosis HSDN C4084724 Usual severity constipation C1855663 Kaufman oculocerebrofacial syndrome MalaCards|HPO C1963154 Renal failure adverse event C1857389 Cystinuria, type b MalaCards C0042571 Vertigo subjective C0017181 Gastrointestinal hemorrhage HSDN C0018991 Paralysis one side of body C1261473 Sarcoma HSDN C0039070 Collapse fleeting C1563715 Andersen syndrome HPO|UMLS C0004134 Dyssynergia C0751279 Metachromatic leukodystrophy, adult-type (disorder) HPO C3541349 Syncope C0002949 Aneurysm, dissecting HSDN C0024031 Back pain lower back C0008073 Developmental disabilities HSDN C0028738 Nystagmus C1859566 Bardet-biedl syndrome 8 HPO C0028738 Nystagmus C1865286 Macrophthalmia, colobomatous, with microcornea MalaCards C0009806 Constipate C1514428 Primary peritoneal carcinoma MalaCards C0042963 Symptoms vomiting C0009062 Clostridia infection HSDN C2096293 Ent surgical result ear vertigo C1000483 Genus anemia HSDN C0349489 Fetal hypoxia C1090821 Sepsis (invertebrate) HSDN C0040264 Ear ringing sound C0022890 Labyrinthine disorder HSDN C3463815 Feel fatigue C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C4085862 Bothered by nausea C0004364 Autoimmune diseases HSDN C0518090 Frequency of pain question C1691228 Cystic kidney diseases HSDN C0015469 Facial paralysis C0026850 Muscular dystrophy HSDN C0042571 Vertigo subjective C0020179 Huntington disease HSDN C4084724 Usual severity constipation C0010308 Congenital hypothyroidism OrphaNet|MalaCards C0042963 Symptoms vomiting C0035956 Rupture spontaneous HSDN C0015230 Exanthem C0021100 Bullous impetigo UMLS C0232943 Metromenorrhagia C0553681 Hypofibrinogenemia MalaCards C1963091 Diarrhea adverse event C0034063 Pulmonary edema HSDN C0518090 Frequency of pain question C0040124 Thyroglossal duct cyst HSDN C1963093 Dizziness adverse event C0035305 Retinal detachment HSDN C0043094 Weight gain C0010692 Cystitis HSDN C0577655 Quadricep weakness C1853926 Nonaka myopathy MalaCards C4084768 Usual severity vomiting C0238386 Cronkhite-canada disease MalaCards C0011168 Disorder deglutition C0032372 Poliomyelitis, anterior, acute DiseaseOntology|MalaCards C0026821 Cramp C0034931 Reflex sympathetic dystrophy HSDN C0851578 Disorder sleep C0042870 Vitamin d deficiency HSDN C0518090 Frequency of pain question C0022336 Creutzfeldt-jakob disease HSDN C0036572 Convulsion C3151753 Combined oxidative phosphorylation deficiency 6 MalaCards|UMLS C0005745 Blepharoptosis C0878675 Erdheim-chester disease MalaCards C0022346 Yellow skin C0027540 Necrosis HSDN C0026826 High muscle tone C2931826 Potassium aggravated myotonia OrphaNet C1963087 Constipation adverse event C0019360 Herpes zoster disease HSDN C0008031 Pain chest C1710501 Pleuropulmonary blastoma type i UMLS C0015676 Mental fatigue C0026857 Musculoskeletal diseases HSDN C3815497 Cough C2930851 Intestinal lipophagic granulomatosis MalaCards C0575081 Abnormal gait C0265289 Metaphyseal chondrodysplasia schmid type MalaCards C0009398 Color vision defects C0008625 Chromosome aberrations HSDN C3641755 Have constipation C0051981 Anti-leprosy vaccine HSDN C3494358 Characteristic, prodromal C0344315 Depressed mood HSDN C4084769 Vomiting frequency C0162576 Anisakiasis HSDN C0019079 Bloody sputum C0022660 Kidney failure, acute HSDN C0019521 Hiccoughs C0014474 Ependymoma HSDN C0036572 Convulsion C0018816 Heart septal defects HSDN C4084727 Cough frequency C3887588 Tracheopathia osteoplastica MalaCards C4084802 Usual severity diarrhea C0019337 Heroin dependence HSDN C0015970 Fever unknown origin C0001175 Acquired immunodeficiency syndrome HSDN|UMLS C0973461 Dysphasia C0282513 Primary progressive aphasia (disorder) HPO C0042571 Vertigo subjective C0018801 Heart failure HSDN C0015672 Decreased energy C1706708 Acute myelomonocytic leukemia without abnormal eosinophils UMLS C0007398 Catatonic C0024906 Masturbation, nos HSDN C4085317 Diarrhea frequency C0026918 Mycobacterium infections HSDN C0518090 Frequency of pain question C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C1962957 Flushing adverse event C2186740 Reported urticaria HSDN C0036572 Convulsion C1336535 Suprasellar meningioma UMLS C0349489 Fetal hypoxia C0004935 Animal ethology HSDN C4084774 Have weight loss C0019196 Hepatitis c HSDN C0013421 Dystonia C0010823 Cytomegalovirus infections HSDN C0018834 Brash C1579931 Depressed - symptom HSDN C1963281 Vomiting adverse event C0341480 Pancreas, cyst, congenital MalaCards C4084726 Distress cough C0010054 Coronary arteriosclerosis HSDN C0030200 Intractable pain C0014804 Erythromelalgia HSDN C0018681 Headache, cephalalgia C0018799 Heart diseases HSDN C0349588 Stature short C1856054 Hutterite cerebroosteonephrodysplasia syndrome MalaCards C0011991 Loose stools C0009663 Condylomata acuminata HSDN C4084725 Usual severity cough C0021361 Female infertility HSDN C2237041 Shox gene with short stature C0220769 Fg syndrome MalaCards|HPO C0038868 Supranuclear palsy progressive C0453996 Tobacco smoking HSDN C0030193 Sense of pain C0037578 Soft tissue injury HSDN C0424755 Fever symptoms C0032326 Pneumothorax HSDN C0020578 Hyperventilate C0020517 Hypersensitivity HSDN C2984058 Have pain C0006262 Bronchial fistula HSDN C3898969 Have been vomiting C0025467 Mesentery, cyst HSDN C0151786 Weakness muscle C0001144 Acne vulgaris HSDN C0019209 Large liver C0342784 Pearson's marrow-pancreas syndrome HPO C0727671 Red cross toothache drops C0037199 Sinusitis HSDN C0015799 Feminisation C0036864 Sexual relations HSDN C0003962 Ascites C0043208 Wolman disease OrphaNet|HPO C0018784 Deafness sensorineural C0007095 Carcinoid tumor HSDN C0476273 Distress respiratory C1761609 Aspiration pneumonitis MalaCards C0152116 Torticollis spasmodic C1869117 Paroxysmal nonkinesigenic dyskinesia HPO C0027066 Myoclonic jerking C2931919 X-linked infantile spasm syndrome MalaCards C4084769 Vomiting frequency C4049644 Depression HSDN C1963091 Diarrhea adverse event C1847835 Vitiligo-associated multiple autoimmune disease susceptibility 1 (finding) HSDN C0234146 Absent reflex C4015038 Myasthenic syndrome, congenital, 7, presynaptic MalaCards C0036659 Sensation disorder C1527311 Brain edema HSDN C0700078 Deep tendon reflex decrease C3280452 Spinocerebellar ataxia, autosomal recessive 12 MalaCards C0037763 Spasm C0026975 Myelitis HSDN C4085317 Diarrhea frequency C0019337 Heroin dependence HSDN C0557874 Global developmental delay C0265372 Fetal hydantoin syndrome OrphaNet|MalaCards C3203358 Alveolar hypoventilation C0038218 Status asthmaticus HSDN C0241137 Skin pallor C0041318 Tuberculosis, meningeal HSDN C4085222 Nausea C0042338 Herpesvirus 3, human HSDN C4084774 Have weight loss C0037579 Soft tissue neoplasms HSDN C1963137 Hydrocephalus adverse event C0795959 Gomez lopez hernandez syndrome OrphaNet|MalaCards C4084725 Usual severity cough C0021799 Interprofessional relations HSDN C0178417 Anhedonia C0022107 Irritable mood HSDN C3463815 Feel fatigue C2981150 Uranostaphyloschisis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0022650 Kidney calculi HSDN C0013456 Pain ear C3489393 Hiatal hernia HSDN C0042755 Virilisation C0001431 Adenoma, basophil HSDN C0035232 Diaphragmatic paralysis C1860808 Triosephosphate isomerase deficiency OrphaNet|HPO C4084768 Usual severity vomiting C0009187 Coccidiosis HSDN C1510417 Apraxia of gait C0026769 Multiple sclerosis HSDN C2911647 Weight gain adverse event C0020655 Hypothalamic diseases HSDN C1963091 Diarrhea adverse event C0022650 Kidney calculi HSDN C0033377 Caudal displacement C0079541 Holoprosencephaly MalaCards C1963249 Tinnitus adverse event C0018799 Heart diseases HSDN C0018772 Deafness C2931557 Chromosome 4 short arm deletion MalaCards C0036572 Convulsion C3711749 Nonsyndromic holoprosencephaly OrphaNet|MalaCards C0018681 Headache, cephalalgia C0393639 Hashimoto's encephalitis MalaCards C1959630 Eye pain adverse event C1830398 Grooming:-:point in time:^patient:- HSDN C4085211 Pain distress question C0009938 Bruising HSDN C1565249 Limitation, mobility C0029941 Brief psychiatric rating scale HSDN C3641756 Have diarrhea C1846171 Lissencephaly, x-linked, 2 HPO C0042571 Vertigo subjective C2717757 Retinocochleocerebral vasculopathies MalaCards C0000727 Abdomen acute C0039128 Syphilis HSDN C0026838 Spasticity muscle C0036916 Sexually transmitted diseases HSDN C0013604 Edematous C0039483 Giant cell arteritis HSDN C0233514 Behavior abnormal C2931197 Waaler aarskog syndrome MalaCards C0497247 Blood pressure elevation C2930930 Abdominal obesity metabolic syndrome MalaCards C0233773 Hallucinations hypnogogic C2919925 Sleep related hallucinations UMLS C4085210 Usual severity pain C0008497 Choriocarcinoma HSDN C0030193 Sense of pain C0018915 Hemangioendothelioma HSDN C4085210 Usual severity pain C0013922 Embolism HSDN C2024893 Cardiovascular surgery result: fatigue C0003811 Cardiac arrhythmia HSDN C0003862 Pain joint C0563150 Catastrophization HSDN C0002962 Angina C0009938 Bruising HSDN C0020673 Hypothermia (central) (local) C0004352 Autistic disorder HSDN C0151786 Weakness muscle C0037019 Shy-drager syndrome HSDN C0042024 Urine incontinence C0015579 Family characteristics HSDN C0009398 Color vision defects C0010038 Corneal opacity HSDN C0151825 Ostalgia C0023903 Liver neoplasms MalaCards C4085211 Pain distress question C0392525 Nephrolithiasis HSDN C4085210 Usual severity pain C0022570 Keratitis dentritic HSDN C4084773 Bothered by weight gain C0004943 Behcet syndrome HSDN C0242936 Center pain C1535939 Pneumocystis jiroveci pneumonia HSDN C0022107 Fussiness C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C1963091 Diarrhea adverse event C0028796 Dermatitis, occupational HSDN C0151786 Weakness muscle C0220847 C hepatitis virus HSDN C2032396 Pelvic pain on the right C0007867 Cervix diseases HSDN C3815497 Cough C0007453 Cattle disease HSDN C0002622 Amnesias C0033936 Psychoses, alcoholic HSDN C4084774 Have weight loss C0035229 Respiratory insufficiency HSDN C0041657 Consciousness loss C0002871 Anemia HSDN C2029884 Hearing loss by exam C0010034 Corneal diseases HSDN C3898969 Have been vomiting C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0018524 Hallucinate C0012644 Animal disease models HSDN C2919142 Short stature adverse event C0796021 Lowry wood syndrome OrphaNet|MalaCards C4085211 Pain distress question C0947622 Cholecystolithiasis HSDN C4084766 Vomiting C0220754 Biotinidase deficiency MalaCards|HPO C0023014 Developmental disorder language C0007787 Transient ischemic attack HSDN C0234378 Postural tremor C1843264 Dystonia 13, torsion MalaCards C2024878 Cardiovascular surgery result: dyspnea C0748540 Scleroderma, limited HSDN C0241157 Skin pustule C0343056 Acute generalized pustular psoriasis MalaCards C0037199 Sinus infection C3809548 Ciliary dyskinesia, primary, 23 MalaCards C3887873 Hearing loss C1962963 Osteoporosis adverse event HSDN C0239836 Hand paresthesia C0030554 Paresthesia UMLS C0018772 Deafness C0796561 Melanoma vaccines HSDN C3829611 Nausea frequency C0001430 Adenoma HSDN C0019521 Hiccoughs C0153413 Malignant neoplasm of upper third of esophagus MalaCards C0267596 Bleeding rectal C0156147 Crohn's disease of large bowel MalaCards C3641755 Have constipation C0013990 Pathological accumulation of air in tissues HSDN C2024893 Cardiovascular surgery result: fatigue C0033289 Family relationship, professional HSDN C2919142 Short stature adverse event C2931366 Congenital deformity of the thumb and congenital alopecia MalaCards C3898969 Have been vomiting C1509147 Histiocytoma HSDN C4084764 Shortness of breath C1535939 Pneumocystis jiroveci pneumonia DiseaseOntology|MalaCards C4085210 Usual severity pain C0005830 Blood protein disorders HSDN C4084766 Vomiting C0028758 Bonding HSDN C0857305 Thrombocytopenia purpura C1963198 Pancreatitis adverse event HSDN C0752210 Paroxysmal dyskinesia C1842534 Dystonia 18 (disorder) OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0018674 Head trauma HSDN C0000737 Abdomen pain C0677779 Hereditary wilms' tumor (wt1) UMLS C0042963 Symptoms vomiting C0268293 Corticosterone methyl oxidase type i deficiency HPO|UMLS C4084727 Cough frequency C0007932 Chagas' disease + no organ inv MalaCards C0016927 Gag reflex C0037899 Sphingolipidoses HSDN C0027497 Queasy C0002395 Alzheimer's disease HSDN C0015672 Decreased energy C0334299 Carcinoid tumor no icd-o subtype HSDN C4084784 Diarrhea C0020635 Hypopituitarism HSDN C0019825 Voice hoarseness C0043251 Wounds and injuries HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0007020 Carbon monoxide poisoning HSDN C0008031 Pain chest C0004623 Bacterial infections HSDN C0040034 Thrombocytopenia C2677299 Cerebroretinal microangiopathy with calcifications and cysts (disorder) HPO C0009806 Constipate C0003857 Congenital arteriovenous malformation HSDN C4084773 Bothered by weight gain C0812393 Cancer patients and suicide and depression HSDN C3463815 Feel fatigue C0031099 Periodontitis HSDN C0002965 Crescendo angina C0007786 Brain ischemia HSDN C3541349 Syncope C1563715 Andersen syndrome HPO C1000483 Genus anemia C0687120 Nephronophthisis OrphaNet|MalaCards C0917816 Deficiency mental C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C0030554 Abnormal sensation C0001973 Alcoholic intoxication, chronic HSDN C0151686 Growth retardation C0339527 Leber congenital amaurosis HPO C0162298 Stiffness joints C0037231 Sjogren-larsson syndrome MalaCards|HPO C0750426 Wbc elevated C0271270 Oculovestibuloauditory syndrome MalaCards C0085593 Chill C0014118 Endocarditis UMLS C2242996 Tingling C3178801 Stroke, lacunar HSDN C4084726 Distress cough C0008925 Cleft palate HSDN C0042024 Urine incontinence C3495422 Finding relating to sexuality and sexual activity HSDN C4085210 Usual severity pain C0027707 Nephritis, interstitial HSDN C0018784 Deafness sensorineural C0027412 Opioid-related disorders HSDN C0033774 Skin pruritus C0036690 Septicemia HSDN C1963091 Diarrhea adverse event C0024668 Mammary neoplasms, experimental HSDN C0025287 Meningitis-like C0003803 Arnold chiari malformation HSDN C4084788 Have dizziness C0018800 Cardiomegaly HSDN C1963252 Tremor adverse event C1860860 Neuhauser daly magnelli syndrome MalaCards C0002962 Angina C0039590 Testicular neoplasms HSDN C0241210 Speaking delay C0432442 Chromosome 18p deletion syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0030977 Perceptual masking HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0749095 Subdural hematoma chronic HSDN C0011991 Loose stools C2936797 Acid cholesteryl ester hydrolase deficiency, type 2 OrphaNet C0040822 D tremors C2706915 Language:-:point in time:^patient:- HSDN C0015938 Fetal macrosomia C0017923 Glycogen storage disease type iv HSDN C0270948 Neurogenic muscular atrophy C1848586 Intestinal pseudoobstruction with external ophthalmoplegia OrphaNet|MalaCards C0151827 Pain eye C0004760 Air pressure-related disorder HSDN C4084784 Diarrhea C0026590 Child mother relationship HSDN C3665492 Pigmentations C3898222 Mucosal melanoma MalaCards C0030193 Sense of pain C1258104 Diffuse scleroderma HSDN C1557397 Adverse event associated with pain C0001622 Adrenal gland hyperfunction HSDN C2919142 Short stature adverse event C2931162 Blepharophimosis radioulnar synostosis OrphaNet|MalaCards C1963091 Diarrhea adverse event C1963266 Uveitis adverse event HSDN C0857305 Thrombocytopenia purpura C0021361 Female infertility HSDN C0027066 Myoclonic jerking C2984289 Melanoma pathway HSDN C1579931 Depressed - symptom C2748910 Rett syndrome, atypical MalaCards C3829611 Nausea frequency C0017168 Gastroesophageal reflux disease HSDN C0426579 Anorexia symptom C1959620 Dihydropyrimidine dehydrogenase deficiency HSDN C4085211 Pain distress question C0024894 Mastitis HSDN C0085636 Light sensitivity C0339277 Corneal dystrophy, juvenile epithelial of meesmann UMLS C0851578 Disorder sleep C0236792 Asperger syndrome HSDN C3898969 Have been vomiting C0162871 Aortic aneurysm, abdominal HSDN C0004604 Pain back C0035358 Retroperitoneal neoplasm HSDN C4084767 Bothered by vomiting C0032269 Pneumococcal infections HSDN C0497247 Blood pressure elevation C1412747 Bbs2 gene HPO C2911645 Weight loss adverse event C0016470 Food allergy HSDN C0375565 Right upper quadrant abdominal rigidity C0810319 Other and unspecified gastrointestinal disorders UMLS C4085661 Usual severity nausea C1550639 Specimen type - fistula HSDN C0037763 Spasm C2937287 Hematolysis HSDN C0036572 Convulsion C0004943 Behcet syndrome MalaCards|HSDN|HPO C0030554 Abnormal sensation C3178970 Entrapment, pudendal nerve MalaCards C0009080 Finger clubbing C1970470 Surfactant metabolism dysfunction, pulmonary, 2 (disorder) MalaCards|HPO C0020903 Illusion C0033367 Projective techniques HSDN C0085631 Abnormal excitement C0010967 Behavior, dangerous HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0029185 Orbit tumor HSDN C0030794 Pelvis pain C0006434 Burn injury HSDN C0015970 Fever unknown origin C0005695 Bladder neoplasm HSDN C3146279 Coma C0002395 Alzheimer's disease HSDN C3641756 Have diarrhea C0314719 Dryness of eye HSDN C4084802 Usual severity diarrhea C0272129 Donath-landsteiner hemolytic anemia MalaCards C0000737 Abdomen pain C0009062 Clostridia infection HSDN C0010200 Cough symptom C0019557 Hip fx HSDN C3887638 Failure to thrive in infant C2931743 Lactate dehydrogenase deficiency type a MalaCards C4084725 Usual severity cough C0004352 Autistic disorder HSDN C0018784 Deafness sensorineural C1961100 Erectile dysfunction adverse event HSDN C4084768 Usual severity vomiting C0025637 Methemoglobinemia HSDN C4084768 Usual severity vomiting C0033054 Prenatal exposure delayed effects HSDN C0009421 Comatose C0016169 Pathologic fistula HSDN C0518090 Frequency of pain question C0153014 Non-arthropod borne lymphocytic choriomeningitis HSDN C0013390 Cramps menstrual C3810814 Myocardial infarction ecg assessment HSDN C0424755 Fever symptoms C0034929 Reflex HSDN C4084769 Vomiting frequency C1090821 Sepsis (invertebrate) HSDN C4084802 Usual severity diarrhea C0033289 Family relationship, professional HSDN C0013362 Dysarthrias C0080040 Polio post syndrome MalaCards C0025323 Bleeding menstrual heavy C0272317 Hereditary factor ii deficiency disease HPO C1549543 Administration method - pain C0162316 Iron deficiency anemia HSDN C0039070 Collapse fleeting C0011616 Contact dermatitis HSDN C3146279 Coma C0031391 Phencyclidine abuse HSDN C1961131 Cough adverse event C0002736 Amyotrophic lateral sclerosis HSDN C0024031 Back pain lower back C0026946 Mycoses HSDN C1279888 Proteinuria of undiagnosed cause C1720821 Membranoproliferative glomerulonephritis, type iii MalaCards C3274924 Have been coughing C0019069 Hemophilia a HSDN C0027796 Neuralgias C0008728 Churg-strauss syndrome HSDN C0028962 Oliguria and anuria nos C0042075 Urologic diseases UMLS C4084802 Usual severity diarrhea C1832322 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive HPO C0037316 Not enough sleeping C0030976 Perceptual distortions HSDN C0242936 Center pain C0040583 Tracheal stenosis HSDN C0008031 Pain chest C0029456 Osteoporosis HSDN C4084723 Constipation C0265498 48, xxxy syndrome OrphaNet|MalaCards C0039231 Heartbeats increased C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0033777 Genital pruritus C0810052 Other inflammatory condition of skin UMLS C0917816 Deficiency mental C3179455 Niemann-pick disease, type c1 MalaCards|HPO C3665386 Abnormal vision C1864669 Neuronal ceroid lipofuscinosis due to cathepsin d deficiency MalaCards|HPO C0018772 Deafness C0041408 Turner syndrome OrphaNet|HSDN|MalaCards C0557874 Global developmental delay C3809278 Epileptic encephalopathy, childhood-onset MalaCards C0033774 Skin pruritus C1552262 Nurse practitioner - family HSDN C0409557 Rubella arthralgia C1300028 Disorder characterised by pain UMLS C0018772 Deafness C0023530 Leukopenia HSDN C0151786 Weakness muscle C1853154 Nemaline myopathy 7 HPO C4085222 Nausea C0025007 Measles HSDN C0030193 Sense of pain C1336358 Paranasal sinus cancer stage iva UMLS C1557397 Adverse event associated with pain C0019337 Heroin dependence HSDN C0427055 Face weakness C0002726 Amyloidosis OrphaNet|MalaCards C4084788 Have dizziness C0033941 Psychoses, substance-induced HSDN C0020452 Engorgement C0019034 Hemoglobin sc disease MalaCards C0012833 Dizzy C0001580 Adolescent behavior HSDN C0018991 Paralysis one side of body C0022410 Joint instability HSDN C3274924 Have been coughing C0025007 Measles DiseaseOntology|HSDN|MalaCards C0018524 Hallucinate C1568249 Usher syndrome, type ii MalaCards|HPO C0011991 Loose stools C0027059 Myocarditis HSDN C1549543 Administration method - pain C1963107 Euphoria adverse event HSDN C3641756 Have diarrhea C0020039 Hostility HSDN C0020673 Hypothermia (central) (local) C2239176 Liver carcinoma HSDN C0042963 Symptoms vomiting C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0004134 Dyssynergia C0268547 Argininosuccinic aciduria OrphaNet|UMLS|HPO|MalaCards C1963184 Nystagmus adverse event C3489725 Pseudo-torch syndrome MalaCards C0040822 D tremors C0751161 Udpglucose 4-epimerase deficiency disease MalaCards C0020672 Body temperature decreased C0026857 Musculoskeletal diseases HSDN C0030552 Paralysis partial C0342643 Autosomal recessive hypophosphatemic vitamin d refractory rickets MalaCards C0241210 Speaking delay C3151113 Meier-gorlin syndrome 3 MalaCards C0030486 Extremity paralysis, lower C0038436 Post-traumatic stress disorder HSDN C0030486 Extremity paralysis, lower C0015802 Femur fracture HSDN C2984058 Have pain C0275148 Poisoning of animal by plant HSDN C0015469 Facial paralysis C0011849 Diabetes mellitus HSDN C0013595 Eczematous dermatitis C1853616 Frontonasal dysplasia and dilated virchow-robin spaces MalaCards C0027497 Queasy C0524812 Intracranial hypotension HSDN C0009421 Comatose C0026769 Multiple sclerosis HSDN C3641756 Have diarrhea C0005779 Blood coagulation disorders HSDN C0013404 Respiratory difficulty C0032290 Aspiration pneumonia HSDN C4084788 Have dizziness C0006309 Brucellosis HSDN C2315100 Pediatric failure to thrive C0342474 Lipoid congenital adrenal hyperplasia OrphaNet C0010200 Cough symptom C1000587 Pemphigus HSDN C4084768 Usual severity vomiting C0007762 Cerebellar neoplasms HSDN C0027066 Myoclonic jerking C0919524 Atm gene HPO C0424755 Fever symptoms C0751951 Central core myopathy (disorder) HPO C0000737 Abdomen pain C0349530 Early gastric cancer UMLS C0042928 Paralysis vocal cord C0011854 Diabetes mellitus, insulin-dependent HSDN C0036659 Sensation disorder C0027813 Neuritis HSDN C0042928 Paralysis vocal cord C0027830 Neurofibroma HSDN C0002170 Alopecia disorders C3281203 Cutaneous telangiectasia and cancer syndrome, familial MalaCards C4084767 Bothered by vomiting C0085423 Gram-negative bacterial infections HSDN C1963281 Vomiting adverse event C0022116 Ischemia HSDN C0003862 Pain joint C0018671 Head and neck neoplasms HSDN C3641755 Have constipation C0009240 Cognition HSDN C1069915 Vertigo C1090821 Sepsis (invertebrate) HSDN C1963091 Diarrhea adverse event C0037072 Diseases sigmoid HSDN C4084767 Bothered by vomiting C0010481 Cushing syndrome HSDN C3665492 Pigmentations C0009197 Cochlear diseases MalaCards C0151205 Periorbital edema C3495801 Granulomatosis with polyangiitis OrphaNet|HPO|MalaCards C0036572 Convulsion C0025292 Haemophilus meningitis HSDN C3665347 Vision impaired C3151139 Retinitis pigmentosa 43 MalaCards|HPO C0497406 Over weight C0001175 Acquired immunodeficiency syndrome HSDN C0036572 Convulsion C0472355 Epilepsy undetermined whether focal or generalised UMLS C0035229 Respiratory function impaired C1739094 Foodborne botulism MalaCards C3539020 Pelvic pain decreasing in frequency C0032966 Complication, neoplastic pregnancy HSDN C0242936 Center pain C0012691 Dislocations HSDN C0010038 Corneal opacity disorder C0013364 Dysautonomia, familial HPO C4084802 Usual severity diarrhea C0206718 Ganglioneuroblastoma HSDN C0042024 Urine incontinence C0007760 Cerebellar diseases HSDN C0242936 Center pain C1334928 Necrotic changes (finding) HSDN C4084776 Weight loss C0282193 Iron overload HSDN C2984058 Have pain C0038354 Stomach diseases HSDN C4084775 Usual severity weight loss C1859407 Bone dysplasia, lethal, holmgren type OrphaNet|MalaCards C0557874 Global developmental delay C2720163 Placental steroid sulfatase deficiency MalaCards C1963281 Vomiting adverse event C0038160 Staphylococcal infections HSDN C0030193 Sense of pain C1266119 Solitary fibrous tumor HSDN C0039070 Collapse fleeting C0877090 Orthostatic collapse UMLS C1963065 Apnea adverse event C0018916 Hemangioma HSDN C0008031 Pain chest C0038833 Superior vena cava syndrome HSDN C0013604 Edematous C0035304 Retinal degeneration HSDN C0035229 Respiratory function impaired C1868594 Perry syndrome MalaCards|HPO C0007758 Cerebellar ataxia C0035091 Renal tubular transport, inborn errors HSDN C1069915 Vertigo C0001430 Adenoma HSDN C0009421 Comatose C0008925 Cleft palate HSDN C4084723 Constipation C0270958 Kocher-debre-semelaigne syndrome OrphaNet|MalaCards C0035229 Respiratory function impaired C0268338 Ehlers-danlos syndrome, type iv OrphaNet|HPO C4084726 Distress cough C0273115 Lung injury HSDN C0234502 Agnosia visual C0155006 Psychophysical visual disturbance, nos UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0008065 Childhood behavior HSDN C3541349 Syncope C0026848 Myopathy HSDN C3887638 Failure to thrive in infant C2240378 Cleft palate on exam HSDN C0030193 Sense of pain C0007762 Cerebellar neoplasms HSDN C2984058 Have pain C3495801 Granulomatosis with polyangiitis HSDN C0040034 Thrombocytopenia C1148551 X-linked dyskeratosis congenita MalaCards|HPO C0034933 Abnormal reflexes C0751785 Unverricht-lundborg syndrome HSDN C0009806 Constipate C0268337 Ehlers-danlos syndrome, type 3 (disorder) OrphaNet|HPO C4084775 Usual severity weight loss C0032227 Pleural effusion disorder HSDN C0030193 Sense of pain C0004239 Atrial flutter HSDN C1549543 Administration method - pain C0018213 Graves disease HSDN C0413252 Hypothermia due to exposure C0010346 Crohn disease HSDN C3641755 Have constipation C0080174 Spina bifida occulta HSDN C0013390 Cramps menstrual C0042266 Vaginismus HSDN C0004134 Dyssynergia C3809216 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 MalaCards|UMLS C0033774 Skin pruritus C1962983 Cataract adverse event HSDN C2096293 Ent surgical result ear vertigo C0002986 Fabry disease MalaCards|HSDN|HPO C0010520 Skin cyanosis C0011570 Mental depression HSDN C0241210 Speaking delay C2931325 Chromosome 22 ring MalaCards C2315100 Pediatric failure to thrive C0016658 Fracture bone HSDN C4085317 Diarrhea frequency C0024694 Mandibular neoplasms HSDN C0231341 Aging premature C2718000 Proteostasis deficiencies HSDN C0454644 Delayed language development C1414025 Dgcr gene HPO C0000737 Abdomen pain C0026269 Mitral valve stenosis HSDN C3887638 Failure to thrive in infant C1439329 Cbs gene HPO C0013421 Dystonia C3279840 Methylmalonate semialdehyde dehydrogenase deficiency MalaCards C0518090 Frequency of pain question C0017400 Behavioral genetics HSDN C4085862 Bothered by nausea C0039239 Sinus tachycardia HSDN C4084769 Vomiting frequency C1963084 Colitis adverse event HSDN C0040034 Thrombocytopenia C0432222 Spondyloenchondrodysplasia MalaCards C4085211 Pain distress question C0020258 Hydrocephalus, normal pressure HSDN C0473385 Edema or excessive weight gain in pregnancy without mention of hypertension, delivered, with or without mention of antepartum condition C0269672 Weight gain pregnancy excessive UMLS C0035229 Respiratory function impaired C0085920 Brachial neuralgia MalaCards C2315100 Pediatric failure to thrive C0033054 Prenatal exposure delayed effects HSDN C3539020 Pelvic pain decreasing in frequency C0029456 Osteoporosis HSDN C3641755 Have constipation C2750784 Spastic paraplegia 44, autosomal recessive (disorder) MalaCards|HPO C0018991 Paralysis one side of body C0032268 Pneumocephalus HSDN C0042963 Symptoms vomiting C0600564 Self-efficacy HSDN C2203646 Jaundice C0005586 Bipolar disorder HSDN C0018777 Deafness, conductive C0033300 Progeria HSDN C4085211 Pain distress question C0032987 Ectopic pregnancy HSDN C0575081 Abnormal gait C0264743 Rheumatic fever without heart involvement MalaCards C0015672 Decreased energy C0027059 Myocarditis HSDN C4084776 Weight loss C0037926 Compression of spinal cord HSDN C0036572 Convulsion C0428478 Serum triglycerides raised HSDN C0005745 Blepharoptosis C3553816 Spinocerebellar ataxia, autosomal recessive 13 MalaCards C4085222 Nausea C0027962 Melanocytic nevus HSDN C0004093 Asthenia C0018995 Hemochromatosis HSDN C2024893 Cardiovascular surgery result: fatigue C2752015 Glycogen storage disease xiv MalaCards C1549543 Administration method - pain C1384672 Hpt gene HSDN C1963093 Dizziness adverse event C0041755 Adverse reaction to drug HSDN C0242936 Center pain C0236733 Amphetamine-related disorders HSDN C0034933 Abnormal reflexes C0028866 Oculomotor nerve paralysis HSDN C1145670 Failure respiratory C0017921 Glycogen storage disease type ii MalaCards|HPO C1963154 Renal failure adverse event C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C0000737 Abdomen pain C0040136 Thyroid neoplasm HSDN C0002962 Angina C0038354 Stomach diseases HSDN C0036659 Sensation disorder C0038048 Sprains and strains HSDN C3887784 Decreased urine output C0001418 Adenocarcinoma HSDN C3541349 Syncope C0007138 Carcinoma, transitional cell HSDN C4084726 Distress cough C0008073 Developmental disabilities HSDN C0033774 Skin pruritus C2931878 Familial primary biliary cirrhosis MalaCards C0151686 Growth retardation C0341306 Microvillus inclusion disease HPO C2984058 Have pain C0030283 Pancreatic cyst HSDN C4084774 Have weight loss C0002989 Epithelioid hemangioma of skin HSDN C2919142 Short stature adverse event C4014386 Mental retardation, autosomal recessive 43 MalaCards C0857305 Thrombocytopenia purpura C0017205 Gaucher disease HSDN C4084725 Usual severity cough C0021831 Intestinal diseases HSDN C0024032 Birth weight subnormal C0044707 11 beta hsd HPO C0016927 Gag reflex C4042784 Feeding and eating disorders HSDN C2919142 Short stature adverse event C1864652 Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate OrphaNet|HPO|MalaCards C0086437 Joint hypermobility C0729582 Floating-harbor syndrome MalaCards|HPO|UMLS C0013604 Edematous C0035357 Retroperitoneal fibrosis HSDN C1963087 Constipation adverse event C0023530 Leukopenia HSDN C0030193 Sense of pain C3889576 Euphoria HSDN C4084767 Bothered by vomiting C0011168 Deglutition disorders HSDN C0030232 Color loss C0346303 Thyrotroph adenoma OrphaNet|MalaCards C1959630 Eye pain adverse event C0399424 Periapical abscess no sinus HSDN C2919142 Short stature adverse event C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C3463815 Feel fatigue C0282333 Relaxation therapies HSDN C3829611 Nausea frequency C0460137 Push down or depress HSDN C0008031 Pain chest C0242973 Ventricular dysfunction HSDN C3539020 Pelvic pain decreasing in frequency C0409354 Flexion contracture of hip HSDN C2919142 Short stature adverse event C0795947 Fryns-van den berghe syndrome OrphaNet|MalaCards C4085317 Diarrhea frequency C0033375 Prolactinoma HSDN C0522224 Palsied C0004421 Avian leukosis HSDN C0424755 Fever symptoms C0027651 Tumor HSDN C2237041 Shox gene with short stature C0553586 Cafe-au-lait macules with pulmonary stenosis OrphaNet|HPO|MalaCards C0427055 Face weakness C2931107 Myasthenic syndrome, congenital, postsynaptic slow-channel MalaCards C0013404 Respiratory difficulty C0271865 Autoimmune hypoparathyroidism MalaCards C0018681 Headache, cephalalgia C1335975 Skull base chordoma UMLS C0241210 Speaking delay C1866504 Photosensitive trichothiodystrophy MalaCards C4084784 Diarrhea C0006277 Bronchitis HSDN C0423742 Intercourse pain C0038325 Stevens-johnson syndrome HPO C0042798 Vision dim C0013238 Dry eye syndromes HSDN C4084774 Have weight loss C0162820 Dermatitis, allergic contact HSDN C0043094 Weight gain C0006736 Body stone HSDN C0851578 Disorder sleep C0026771 Trauma multiple HSDN C0003079 Pupillary inequality C0271355 Abducens nerve paralysis HSDN C0031911 Pigment deposition C1848410 Xeroderma pigmentosum, variant type MalaCards C0234471 Conduction aphasia C0751396 Well differentiated oligodendroglioma HSDN C0003862 Pain joint C0019699 Hiv seropositivity HSDN C0018681 Headache, cephalalgia C1332963 Childhood choroid plexus papilloma UMLS C0232726 Tenesmus, rectal C2981228 Stage ii rectosigmoid cancer ajcc v6 UMLS C0000737 Abdomen pain C0233315 Premature birth of newborn HSDN C0002170 Alopecia disorders C0041408 Turner syndrome MalaCards C0018772 Deafness C0024228 Lymphatic diseases HSDN C1549543 Administration method - pain C0035304 Retinal degeneration HSDN C0221752 Rbc urine C0034155 Purpura, thrombotic thrombocytopenic MalaCards|HSDN C4084769 Vomiting frequency C0162869 Aneurysm, ruptured HSDN C0042963 Symptoms vomiting C0861855 Bile duct clear cell adenocarcinoma UMLS C0850758 Pain pelvic C0029456 Osteoporosis HSDN C0011991 Loose stools C0001206 Acromegaly HSDN C3887638 Failure to thrive in infant C0027888 Hereditary motor and sensory neuropathies HSDN C0043144 Wheeze C0812341 Latex allergy response UMLS C0020673 Hypothermia (central) (local) C0032965 Pregnancy complications, infectious HSDN C0030193 Sense of pain C0242231 Coronary stenosis HSDN C3887638 Failure to thrive in infant C0011981 Diaphragmatic eventration HSDN C1963180 Neck pain adverse event C0524620 Metabolic syndrome x HSDN C1000483 Genus anemia C1842704 Gaucher disease, perinatal lethal MalaCards|HPO C4085641 Level of joint pain C1832998 Epiphyseal dysplasia, multiple, 3 MalaCards C0018926 Emesis bloody C0221752 Rbc urine HSDN C0027497 Queasy C0867389 Chronic graft-versus-host disease MalaCards C4084767 Bothered by vomiting C1845892 Hprt deficiency, neurologic variant HPO C0857305 Thrombocytopenia purpura C0019050 Hemoglobinuria, paroxysmal HSDN C0151818 Opisthotonos C1854989 Molybdenum cofactor deficiency, complementation group b HPO|UMLS C3812171 Bradycardia by ecg finding C2931516 Hyde forster mccarthy berry syndrome MalaCards C4085548 Usual severity dizziness C0013295 Duodenal ulcer HSDN C0042940 Disorder of voice C0013423 Dystonia musculorum deformans HSDN C3641756 Have diarrhea C0268525 5-oxoprolinase deficiency MalaCards|HPO C0036572 Convulsion C0027126 Myotonic dystrophy HSDN C4084802 Usual severity diarrhea C0025323 Menorrhagia HSDN C0042571 Vertigo subjective C0027643 Neoplasm recurrence, local HSDN C4084773 Bothered by weight gain C0013808 Electroconvulsive therapy HSDN C0277799 Fever intermittent C2748568 Immune dysfunction with t-cell inactivation due to calcium entry defect 1 MalaCards|HPO C0033377 Caudal displacement C0796121 Primrose syndrome MalaCards|HPO C0026838 Spasticity muscle C0268595 Glutaric aciduria, type 1 OrphaNet|HPO C1963065 Apnea adverse event C0002989 Epithelioid hemangioma of skin HSDN C0149758 Dentition poor C0011334 Dental caries UMLS C4084769 Vomiting frequency C0019069 Hemophilia a HSDN C0042940 Disorder of voice C0079943 Oral fistulas HSDN C0008031 Pain chest C4049644 Depression HSDN C0031911 Pigment deposition C1855465 Stargardt disease 1 (disorder) MalaCards C4084775 Usual severity weight loss C0206629 Pulmonary blastoma OrphaNet|MalaCards C4085317 Diarrhea frequency C0019655 Histoplasmosis HSDN C0426579 Anorexia symptom C0085632 Apathy HSDN C0004134 Dyssynergia C0175683 Citrullinemia HPO|UMLS C0015468 Face pain C0028432 Nose diseases HSDN C0038868 Supranuclear palsy progressive C2936349 Plaque, amyloid HSDN C0016927 Gag reflex C0004415 Aversion therapy HSDN C0034124 Pupillary disorder C0014877 Esotropia HSDN C0011991 Loose stools C0033247 Proctocolitis HSDN C0015672 Decreased energy C0009207 Cockayne syndrome MalaCards C2024893 Cardiovascular surgery result: fatigue C0814263 Meditation therapy HSDN C0040822 D tremors C1851945 Dystonia 1, torsion, autosomal dominant HPO|UMLS C4042891 Sleep wake disorders C0004937 Behavioral medicine HSDN C0030193 Sense of pain C0393829 Acute painful diab neuropathy UMLS C4084776 Weight loss C0016663 Pathological fracture HSDN C1860844 Sparse, thin hair C3809005 Cardiofaciocutaneous syndrome 2 MalaCards C3829611 Nausea frequency C0023343 Leprosy HSDN C2203646 Jaundice C0003493 Aortic diseases HSDN C2984058 Have pain C0009952 Febrile convulsions HSDN C0013604 Edematous C0032019 Pituitary neoplasms HSDN C0020672 Body temperature decreased C0001807 Aggressive behavior HSDN C0019572 Hairiness C1412746 Bbs1 gene HPO C4084767 Bothered by vomiting C0022729 Klebsiella infections HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0282607 Vascular neoplasms HSDN C2048468 Inability to impregnate C0041409 Turner syndrome, male MalaCards|HPO C0023380 Lethargy C0268450 Gitelman syndrome HSDN C3829611 Nausea frequency C0014868 Esophagitis HSDN C2032395 Pelvic pain on the left C0085096 Peripheral vascular diseases HSDN C0234376 Tremor action C2750220 Karak syndrome MalaCards|HPO C0036572 Convulsion C0220769 Fg syndrome MalaCards|HPO|UMLS C4084723 Constipation C0343377 C; paratyphoid fever DiseaseOntology|MalaCards C0027497 Queasy C0000833 Abscess HSDN C0018772 Deafness C0019104 Hemorrhagic fevers, viral MalaCards C4085210 Usual severity pain C0030421 Paraganglioma HSDN C4084725 Usual severity cough C0037397 Behavior social HSDN C0003862 Pain joint C0022976 Animal gait disorder HSDN C0740418 Back pain chronic C0750217 Vertebra disc bulging UMLS C1279888 Proteinuria of undiagnosed cause C0025007 Measles HSDN C4084767 Bothered by vomiting C0264766 Rheumatic mitral stenosis HSDN C0043094 Weight gain C0014347 Enterobacteriaceae infections HSDN C1962972 Proteinuria adverse event C0020557 Hypertriglyceridemia HSDN C0013604 Edematous C0005591 Avian disease HSDN C2237041 Shox gene with short stature C2752041 Three m syndrome 2 HPO C3641755 Have constipation C0021603 Sleep initiation and maintenance disorders HSDN C4085317 Diarrhea frequency C0042994 Vulvar diseases HSDN C0013362 Dysarthrias C0085220 Cerebral amyloid angiopathy HSDN C0036572 Convulsion C1835171 Hypomagnesemia 2, renal MalaCards|HPO|UMLS C1962972 Proteinuria adverse event C1839874 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis OrphaNet C3829611 Nausea frequency C2981150 Uranostaphyloschisis HSDN C0013405 Dyspnea, paroxysmal C3827868 Tachycardia by ecg finding HSDN C2237041 Shox gene with short stature C1859773 Microphthalmia, syndromic 3 MalaCards|HPO C0018681 Headache, cephalalgia C0062527 Hepatitis b vaccine HSDN C4084775 Usual severity weight loss C2750074 Rhabdoid tumor predisposition syndrome 2 MalaCards C4084769 Vomiting frequency C1509147 Histiocytoma HSDN C0009806 Constipate C0036341 Schizophrenia HSDN C0242936 Center pain C1145670 Respiratory failure HSDN C0042024 Urine incontinence C1704436 Peripheral arterial diseases HSDN C2242996 Tingling C0030581 Parotid neoplasms HSDN C0003862 Pain joint C0343101 Wells syndrome MalaCards C0027796 Neuralgias C0018213 Graves disease HSDN C0024031 Back pain lower back C0423682 Mechanical low back pain UMLS C4084727 Cough frequency C1962979 Burn adverse event HSDN C1963170 Hypothermia adverse event C0001627 Congenital adrenal hyperplasia HSDN C0034124 Pupillary disorder C0037019 Shy-drager syndrome HSDN C0518090 Frequency of pain question C0032780 Postmortem changes HSDN C0011991 Loose stools C0008519 Ectopic tissue HSDN C3146279 Coma C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO C0027066 Myoclonic jerking C0009375 Colonic neoplasms HSDN C0011175 Deficient fluid volume C1565489 Renal insufficiency MalaCards C0403569 Pain during outflow of dialysate C1300028 Disorder characterised by pain UMLS C0015469 Facial paralysis C0009241 Cognition disorders HSDN C1384666 Decreased hearing C0042384 Vasculitis HSDN C1963091 Diarrhea adverse event C0024788 Green monkey virus disease DiseaseOntology|OrphaNet|MalaCards C0085593 Chill C0005716 Blastomycosis HSDN C4084769 Vomiting frequency C0031485 Phenylketonurias HSDN C0011991 Loose stools C0002871 Anemia HSDN C0018991 Paralysis one side of body C0085183 Neoplasms, second primary HSDN C0030975 Disorders perception C0376542 Cognitive science HSDN C0019572 Hairiness C1720860 Familial partial lipodystrophy, type 2 HPO C0237326 Defecation pain C1956093 Paris-trousseau thrombocytopenia MalaCards C0878638 Tongue signs C1849382 Familial rhizomelic dysplasia OrphaNet|MalaCards C0009763 Conjunctiva inflammation C0162530 Porphyria, erythropoietic HPO C0040822 D tremors C1704421 Skin pigmentation disorder HSDN C1963086 Confusion adverse event C0036356 Schizophrenics--language HSDN C0013404 Respiratory difficulty C1527226 Crst syndrome MalaCards C1963093 Dizziness adverse event C0041582 Ulcer HSDN C0026826 High muscle tone C0393591 Aicardi-goutieres syndrome OrphaNet|MalaCards C4085641 Level of joint pain C0524909 Hepatitis b, chronic MalaCards C0917816 Deficiency mental C3891556 Chromosome xq26.3 duplication syndrome MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0040381 Syndrome tolosa-hunt HSDN C2237041 Shox gene with short stature C1327915 Congenital amegakaryocytic thrombocytopenia OrphaNet|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C2186740 Reported urticaria HSDN C4085211 Pain distress question C0221391 Melanosis coli HSDN C0745112 Hypertension accelerated symptom C0403447 Chronic kidney insufficiency UMLS C4084768 Usual severity vomiting C0023418 Leukemia HSDN C0036572 Convulsion C0342284 Bangstad syndrome OrphaNet|MalaCards C3665347 Vision impaired C2746069 Familial ectopia lentis MalaCards|HPO C0018772 Deafness C0002991 Cutaneous fibrous histiocytoma HSDN C0497247 Blood pressure elevation C1567743 Alport syndrome, autosomal dominant MalaCards|HPO C3827868 Tachycardia by ecg finding C0391817 Drug-induced autoim haem anaem MalaCards C0011991 Loose stools C0019360 Herpes zoster disease HSDN C1963091 Diarrhea adverse event C0009766 Allergic conjunctivitis HSDN C0085631 Abnormal excitement C0018799 Heart diseases HSDN C0005745 Blepharoptosis C0553586 Cafe-au-lait macules with pulmonary stenosis OrphaNet|HPO|MalaCards C0497406 Over weight C0036875 Disorders of sex development HSDN C0042571 Vertigo subjective C0023343 Leprosy HSDN C1963184 Nystagmus adverse event C0029454 Osteopetrosis MalaCards C0518090 Frequency of pain question C0007781 Intracranial embolism and thrombosis HSDN C0020580 Decreased sensation C1833809 Optic atrophy and cataract, autosomal dominant OrphaNet C0034150 Skin purpura C0035053 Spontaneous remission HSDN C0020672 Body temperature decreased C0014335 Enteritis HSDN C4084768 Usual severity vomiting C0206172 Diabetic foot HSDN C4084727 Cough frequency C0085167 Granular cell tumor HSDN C1549543 Administration method - pain C0035436 Rheumatic fever HSDN C0019079 Bloody sputum C0012979 Canine disease HSDN C3898969 Have been vomiting C0023470 Myeloid leukemia HSDN C0037317 Sleep disturbance C0859942 Hanot's cirrhosis MalaCards C4084802 Usual severity diarrhea C0015230 Exanthema HSDN C0011168 Disorder deglutition C0079474 Hallopeau-siemens disease MalaCards|HPO C0727671 Red cross toothache drops C0007137 Squamous cell carcinoma HSDN C0233514 Behavior abnormal C0268642 Histidinuria renal tubular defect MalaCards C1963281 Vomiting adverse event C0036095 Salivary gland neoplasms HSDN C0232466 Feeding difficulty C2749862 Mitochondrial neurogastrointestinal encephalopathy syndrome, rrm2b-related HPO C0011991 Loose stools C0011881 Diabetic nephropathy HSDN C0030193 Sense of pain C0003646 Aptitude HSDN C0020505 Excessive eating C0030567 Parkinson disease HSDN C0015970 Fever unknown origin C0025162 Megacolon toxic HSDN C0751706 Aphasia, progressive nonfluent C3714605 Of pain perception HSDN C0004604 Pain back C0027627 Neoplasm metastasis HSDN C0494475 Seizure generalized tonic clonic C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C0015672 Decreased energy C0021890 Intraoperative complications HSDN C0015672 Decreased energy C0021655 Insulin resistance HSDN C3463815 Feel fatigue C0019557 Hip fx HSDN C1579931 Depressed - symptom C1868594 Perry syndrome OrphaNet|HPO|MalaCards C0041105 Jaw spasm C0024953 Maxilla fracture HSDN C4084776 Weight loss C0085426 Gram-positive bacterial infections HSDN C0004134 Dyssynergia C3887654 Polyarteritis nodosa, childhood-onset MalaCards|UMLS C0040822 D tremors C0039336 Gustatory sense HSDN C3146279 Coma C0268193 Nadh cytochrome b5 reductase deficiency HPO C0237326 Defecation pain C2748910 Rett syndrome, atypical MalaCards|HPO C3665492 Pigmentations C1857821 Leber congenital amaurosis 10 (disorder) MalaCards C0018681 Headache, cephalalgia C1332204 Adult leptomeningeal melanoma UMLS C0011206 Delirium acute C0439840 Reflex motion descriptor HSDN C0413252 Hypothermia due to exposure C1962971 Myocarditis adverse event HSDN C0007758 Cerebellar ataxia C1836383 Spinocerebellar ataxia 27 UMLS C0013404 Respiratory difficulty C0010418 Cryptosporidiosis HSDN C4084784 Diarrhea C0241802 Arthritis, venereal MalaCards C4084766 Vomiting C1275126 Tnf receptor-associated periodic fever syndrome (traps) OrphaNet|HPO C0013395 Indigestion C0004238 Atrial fibrillation HSDN C0018784 Deafness sensorineural C0162872 Aortic aneurysm, thoracic HSDN C0007814 Cerebrospinal fluid otorrhea C0018944 Hematoma HSDN C2024893 Cardiovascular surgery result: fatigue C1299919 Enteric coccidiosis HSDN C2242996 Tingling C0038525 Subarachnoid hemorrhage HSDN C0030552 Paralysis partial C0751549 Neurogenic thoracic outlet syndrome MalaCards C0016199 Pain flank C1704212 Embolism embolus HSDN C0022568 Inflammation corneal C1848411 Xeroderma pigmentosum, complementation group e HPO C4084784 Diarrhea C0030353 Papilledema HSDN C0036572 Convulsion C0017920 Glycogen storage disease type i OrphaNet|MalaCards C0018777 Deafness, conductive C0524948 Maxillofacial abnormalities HSDN C0018780 Frequencies hearing high loss C1261128 Progeria-like syndrome MalaCards C4084773 Bothered by weight gain C0702166 Acne HSDN C2219909 Sexual identity is different from one's anatomic sex C0011253 Delusions UMLS C0497406 Over weight C3244301 Coverage level - family HSDN C4084773 Bothered by weight gain C0016514 Foot-and-mouth disease HSDN C1260880 Nasal drip C1336311 Paranasal sinus cancer stage ii UMLS C0030193 Sense of pain C0024692 Mandible fracture HSDN C0162298 Stiffness joints C1832998 Epiphyseal dysplasia, multiple, 3 MalaCards C3665386 Abnormal vision C0268342 Ehlers-danlos syndrome type 6 MalaCards C4085317 Diarrhea frequency C0010481 Cushing syndrome HSDN C3541349 Syncope C0022665 Kidney neoplasm HSDN C1963086 Confusion adverse event C0453996 Tobacco smoking HSDN C0424755 Fever symptoms C0030521 Parathyroid neoplasms HSDN C1963281 Vomiting adverse event C4085635 Appetite quality question HSDN C2203646 Jaundice C0037369 Smoking HSDN C0917816 Deficiency mental C1845862 Creatine deficiency, x-linked OrphaNet|HPO|MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0036310 Scheuermann's disease HSDN C4084773 Bothered by weight gain C0037275 Skin diseases, vesiculobullous HSDN C0036572 Convulsion C0038395 Streptococcal infections HSDN C3829611 Nausea frequency C0020437 Hypercalcemia HSDN C2919142 Short stature adverse event C1832812 Cataracts, congenital, with sensorineural deafness, down syndrome-like facial appearance, short stature, and mental retardation HPO C3641755 Have constipation C1394494 Cystocele, unspecified HSDN C0002624 Amnesia retrograde C0011570 Mental depression HSDN C4084784 Diarrhea C1962976 Ventricular fibrillation adverse event HSDN C4084769 Vomiting frequency C0038362 Stomatitis HSDN C0035229 Respiratory function impaired C1961835 Gaucher disease, type 1 MalaCards C0011991 Loose stools C0023470 Myeloid leukemia HSDN C0020455 Hypergammaglobulinemia C0206255 Malaria vaccine HSDN C0019079 Bloody sputum C1708782 Signet ring cell carcinoma of lung UMLS C4084766 Vomiting C1563705 Nephrogenic diabetes insipidus, type i HPO C2237041 Shox gene with short stature C0015934 Fetal growth retardation MalaCards C1963086 Confusion adverse event C0393642 Sepsis-associated encephalopathy HSDN C0020538 Hbp C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C0232466 Feeding difficulty C1969084 Pontocerebellar hypoplasia type 6 MalaCards C0008031 Pain chest C1708957 Mediastinal paraganglioma UMLS C1145670 Failure respiratory C0268647 Lysinuric protein intolerance MalaCards|HPO C4084802 Usual severity diarrhea C0014121 Bacterial endocarditis HSDN C0587047 Mass of trunk C0009663 Condylomata acuminata UMLS C0003811 Cardiac rhythm disturbance C2748910 Rett syndrome, atypical MalaCards C3887873 Hearing loss C0010709 Cyst HSDN C4084802 Usual severity diarrhea C1963274 Vasculitis adverse event HSDN C3539890 Pelvic pain causes awakening at night C0042996 Vulvitis unspecified HSDN C4085642 Level of joint stiffness C0432239 Kyphomelic dysplasia OrphaNet|MalaCards C4020887 Photodysphoria C2751316 Glaucoma 3, primary congenital, d MalaCards|HPO C4084776 Weight loss C0013080 Down syndrome HSDN C0019214 Hepatosplenomegaly C0343376 B; paratyphoid fever DiseaseOntology|MalaCards C0036572 Convulsion C0028880 Odontogenic tumors HSDN C0751495 Seizure focal C1336537 Supratentorial meningioma MalaCards C2237041 Shox gene with short stature C3810175 Short-rib thoracic dysplasia 10 with or without polydactyly MalaCards C2203646 Jaundice C0036341 Schizophrenia HSDN C3887873 Hearing loss C0011989 Camurati-engelmann syndrome HSDN C0233794 Memory impaired C0017495 Gerstmann-straussler-scheinker disease MalaCards|HPO C0030552 Paralysis partial C3150692 Amyotrophic lateral sclerosis 12 MalaCards|HPO C0036572 Convulsion C0282207 Cronkhite-canada syndrome MalaCards C0028961 Urine output decreased C0036415 Sclerema neonatorum nos HSDN C0004134 Dyssynergia C1968552 Mental retardation, x-linked, with spasticity HPO C0004941 Behavioral symptoms C0751587 Cadasil syndrome HPO C0007814 Cerebrospinal fluid otorrhea C0009197 Cochlear diseases HSDN C0151686 Growth retardation C1864499 Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss HPO C0042798 Vision dim C0038661 Suicide HSDN C4084773 Bothered by weight gain C0023441 Leukemia, experimental HSDN C0037316 Not enough sleeping C0023890 Liver cirrhosis HSDN C0030486 Extremity paralysis, lower C0015306 Hereditary multiple exostoses HSDN C0557874 Global developmental delay C3890168 Mental retardation, x-linked 101 MalaCards C1999266 Depression adverse event C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C0497406 Over weight C0007124 Noninfiltrating intraductal carcinoma HSDN C4084784 Diarrhea C0041466 Typhoid fever DiseaseOntology|HSDN|MalaCards C4085317 Diarrhea frequency C0004144 Atelectasis HSDN C0848203 Male pelvic pain C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C3541349 Syncope C0950124 Papillomavirus infections HSDN C3887638 Failure to thrive in infant C0012236 Digeorge syndrome MalaCards|HSDN|HPO C0700078 Deep tendon reflex decrease C3150897 Charcot-marie-tooth disease, recessive intermediate b HPO C0242936 Center pain C0013473 Eating disorders HSDN C1963170 Hypothermia adverse event C0014118 Endocarditis HSDN C0019209 Large liver C1855114 Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency OrphaNet|HPO C2984057 Have nausea C0033923 Psychomotor function HSDN C0742292 Chest pain char typical C0004239 Atrial flutter UMLS C0424755 Fever symptoms C0152173 Ventricular flutter HSDN C0028738 Nystagmus C0751268 Encephalopathy, subacute necrotizing, juvenile MalaCards C0042024 Urine incontinence C0024437 Macular degeneration HSDN C0018772 Deafness C0007795 Diffuse cerebral sclerosis of schilder MalaCards C1963093 Dizziness adverse event C0007137 Squamous cell carcinoma HSDN C0020450 Hyperemesis gravidarum C0018802 Congestive heart failure HSDN C0042024 Urine incontinence C0009475 Community mental health service HSDN C0015970 Fever unknown origin C0750394 Wbc low HSDN C0019825 Voice hoarseness C0026267 Mitral valve prolapse syndrome HSDN C0011991 Loose stools C0002940 Aneurysm HSDN C0232466 Feeding difficulty C2751067 Parkinsonism-dystonia, infantile MalaCards|HPO C0750403 Weakness proximal C0574083 3-methylglutaconic aciduria type 2 MalaCards|UMLS C0036572 Convulsion C3553831 Microcephaly, short stature, and polymicrogyria with or without seizures UMLS C0727671 Red cross toothache drops C0017563 Gingival diseases HSDN C0018784 Deafness sensorineural C0013261 Duane retraction syndrome OrphaNet|HPO|MalaCards C0727671 Red cross toothache drops C0032787 Postoperative complications HSDN C4084776 Weight loss C0265235 Marshall syndrome MalaCards C0009676 Confusion state C0393639 Hashimoto's encephalitis OrphaNet|MalaCards C2029884 Hearing loss by exam C0241158 Cicatrix skin HSDN C0039231 Heartbeats increased C2931232 Ventricular extrasystoles perodactyly robin sequence MalaCards C0040822 D tremors C0015397 Disorder of eye HSDN C1950154 Insomnia homeopathic medication C1997249 Neuralgia, pudendal MalaCards C0042024 Urine incontinence C0003811 Cardiac arrhythmia HSDN C2203646 Jaundice C0085293 Hepatitis e MalaCards C0030552 Paralysis partial C0268407 Senile cardiac amyloidosis MalaCards C0015970 Fever unknown origin C0018915 Hemangioendothelioma HSDN C2024878 Cardiovascular surgery result: dyspnea C0032787 Postoperative complications HSDN C0007758 Cerebellar ataxia C0039373 Tay-sachs disease OrphaNet|MalaCards C0023015 Language handicap C0752347 Lewy body disease HSDN C2585546 Left lower quadrant abdominal rigidity C0810319 Other and unspecified gastrointestinal disorders UMLS C1519353 Skin eruption papular C1266181 Dysplastic gangliocytoma of cerebellum (lhermitte-duclos) OrphaNet|HPO|MalaCards C0020580 Decreased sensation C4014371 Immunodeficiency 23 MalaCards C4085661 Usual severity nausea C0220847 C hepatitis virus HSDN C4085642 Level of joint stiffness C3714043 Trisomy xq28 HPO C1963093 Dizziness adverse event C0002895 Anemia, sickle cell HSDN C0522224 Palsied C0027059 Myocarditis HSDN C1963281 Vomiting adverse event C0005586 Bipolar disorder HSDN C0398650 Idiopathic thrombocytopenia purpura C0020517 Hypersensitivity HSDN C1962956 Flatulence adverse event C0009373 Colonic diseases HSDN C0011570 Monopolar depression C3280358 Wolfram-like syndrome, autosomal dominant OrphaNet|HPO|MalaCards C3463815 Feel fatigue C0035436 Rheumatic fever OrphaNet|HSDN|MalaCards C3146279 Coma C0008065 Childhood behavior HSDN C0151889 Reflexes tendon increased C1849322 Sandhoff disease, infantile type HPO C3829611 Nausea frequency C0023176 Lead poisoning HSDN C0034933 Abnormal reflexes C0015409 Eye injuries penetrating HSDN C1384666 Decreased hearing C0017416 Genital neoplasms, female HSDN C4084774 Have weight loss C0282193 Iron overload HSDN C2032396 Pelvic pain on the right C0010068 Coronary heart disease HSDN C4084726 Distress cough C0007932 Chagas' disease + no organ inv MalaCards C0013362 Dysarthrias C0751778 Myoclonic epilepsies, progressive HSDN C1961131 Cough adverse event C1955864 Cardiac sinus arrest HSDN C0241210 Speaking delay C2674949 Chromosome 3q29 deletion syndrome OrphaNet|MalaCards C1971624 Appetite absent C0004936 Mental disorders HSDN C0032617 High urine output C0001430 Adenoma HSDN C0557874 Global developmental delay C0796095 Opitz trigonocephaly syndrome MalaCards|HPO C2108948 Joint pain in ring finger of left hand increased by lifting object C1862100 Brachydactyly-ectrodactyly with fibular aplasia or hypoplasia MalaCards C4084776 Weight loss C0021845 Intestinal perforation HSDN C1963164 Lymphopenia adverse event C0043194 Wiskott-aldrich syndrome OrphaNet|HPO|MalaCards C1384666 Decreased hearing C0014065 Congenital cerebral hernia HSDN C3898969 Have been vomiting C0039841 Thiamine deficiency HSDN C2984058 Have pain C0018924 Hemarthrosis HSDN C0277873 Nasal flaring C0034345 Pyruvate dehydrogenase complex deficiency disease MalaCards|HPO C3463815 Feel fatigue C0700327 Clinical findings relating to memory HSDN C2096293 Ent surgical result ear vertigo C0338078 Non-functioning pituitary gland neoplasm MalaCards C4084774 Have weight loss C0020445 Hypercholesterolemia, familial HSDN C0522224 Palsied C0042140 Uterine prolapse HSDN C0035229 Respiratory function impaired C2677590 Congenital disorder of glycosylation, type in MalaCards|HPO C0040460 Dental pain C3714605 Of pain perception HSDN C0497247 Blood pressure elevation C2676192 Somatostatin analog, resistance to HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007133 Carcinoma, papillary HSDN C0497247 Blood pressure elevation C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency OrphaNet|HPO C4085210 Usual severity pain C0013240 Alveolar osteitis HSDN C4082202 Sleep quality question C0751362 Narcolepsy-cataplexy syndrome MalaCards C0009806 Constipate C1335686 Neuroendocrine neoplasm of rectum MalaCards C0020580 Decreased sensation C1956346 Coronary artery disease HSDN C0557874 Global developmental delay C0342191 Familial dyshormonogenetic goiter MalaCards C1279888 Proteinuria of undiagnosed cause C0151744 Myocardial ischemia HSDN C0009676 Confusion state C0023895 Liver diseases HSDN C4085211 Pain distress question C1285666 Drinking behavior HSDN C4085862 Bothered by nausea C0033817 Pseudomonas infections HSDN C0027497 Queasy C1856401 Etfa deficiencies HPO C1963281 Vomiting adverse event C0025500 Mesothelioma HSDN C0002965 Crescendo angina C0009324 Ulcerative colitis HSDN C4084726 Distress cough C0025061 Disease of mediastinum HSDN C0030193 Sense of pain C3862127 Varicose veins of bilateral legs with pain UMLS C0037383 Sneeze C0009763 Conjunctivitis HSDN C0557874 Global developmental delay C2673648 Hypomagnesemia 4, renal MalaCards|HPO C3463815 Feel fatigue C1836439 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3 MalaCards|HPO C0857305 Thrombocytopenia purpura C0040136 Thyroid neoplasm HSDN C1963281 Vomiting adverse event C0265323 Peutz-jeghers hamartoma of small bowel MalaCards C0152459 Striae C4014425 Pigmented nodular adrenocortical disease, primary, 4 MalaCards C0013911 Emaciate C0003850 Arteriosclerosis HSDN C4085317 Diarrhea frequency C0023441 Leukemia, experimental HSDN C0034933 Abnormal reflexes C0015401 Foreign body in eye HSDN C0522224 Palsied C0014347 Enterobacteriaceae infections HSDN C0018784 Deafness sensorineural C0023786 Mucopolysaccharidosis i OrphaNet C2017238 Left leg soft tissue swelling with bluish discoloration C0037580 Soft tissue swelling UMLS C0020538 Hbp C0040028 Thrombocythemia, essential HPO C1963087 Constipation adverse event C1306794 Wound botulism OrphaNet|MalaCards C4085210 Usual severity pain C0001621 Adrenal gland diseases HSDN C0018772 Deafness C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C4084776 Weight loss C0036341 Schizophrenia HSDN C2024878 Cardiovascular surgery result: dyspnea C1969343 Pulmonary hypertension, primary, fenfluramine-associated HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0376545 Hematologic neoplasms HSDN C4084766 Vomiting C0007097 Carcinomas HSDN C0456073 Neonatal facial petechiae C1290028 Disease of skin and/or subcutaneous tissue of head UMLS C4084776 Weight loss C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0011206 Delirium acute C0027765 Nervous system disorder HSDN C4084767 Bothered by vomiting C2937287 Hematolysis HSDN C3665492 Pigmentations C1514422 Primary glioblastoma MalaCards C0030552 Paralysis partial C0035242 Respiratory tract diseases HSDN C2984058 Have pain C0030922 Peptic ulcer hemorrhage HSDN C0424755 Fever symptoms C0030330 Panniculitis, peritoneal HSDN C2203646 Jaundice C0431693 Renal cysts and diabetes syndrome MalaCards|HPO C4085862 Bothered by nausea C0524851 Neurodegenerative disorders HSDN C0034150 Skin purpura C3827868 Tachycardia by ecg finding HSDN C0031911 Pigment deposition C1704216 Basaloid carcinoma MalaCards C0015672 Decreased energy C0030767 Grouping peer HSDN C0231531 Fibrillation muscle C0242287 Isaacs syndrome OrphaNet|MalaCards C0010200 Cough symptom C0026896 Myasthenia gravis HSDN C0004134 Dyssynergia C1835614 Hereditary hyperexplexia MalaCards C0042963 Symptoms vomiting C0022661 Kidney failure, chronic HSDN C4084726 Distress cough C0012691 Dislocations HSDN C0264599 Aphonia paralytica C0264625 Vocal nodules in adults UMLS C0232493 Epigastric pain C0025222 Melena UMLS C2127533 Elbow joint pain exacerbated by rotating wrist clockwise C1862162 Brachydactyly preaxial with hallux varus and thumb abduction MalaCards C0751295 Memory loss or impairment C0009405 Hereditary nonpolyposis colorectal neoplasms MalaCards C1557397 Adverse event associated with pain C0012752 Distance discrimination HSDN C0424755 Fever symptoms C0276386 Mosquito-borne viral fever, oropouche MalaCards C0518090 Frequency of pain question C0039614 Tetanus HSDN C0497406 Over weight C0038358 Gastric ulcer HSDN C3641755 Have constipation C0344490 Sacral agenesis HPO C0015672 Decreased energy C0242658 Homosexuality male HSDN C0038506 Stutter C0270857 Epilepsy, reflex HSDN C4085222 Nausea C1579931 Depressed - symptom HSDN C4085210 Usual severity pain C0003618 Appetites HSDN C3541349 Syncope C1865020 Short qt syndrome 1 MalaCards|HPO C1963249 Tinnitus adverse event C0029440 Osteoma HSDN C0030193 Sense of pain C1513365 Breast carcinosarcoma UMLS C0231218 Malaise generalized C2047937 Ill-defined condition UMLS C3887638 Failure to thrive in infant C0085110 Severe combined immunodeficiency OrphaNet|MalaCards C3815497 Cough C0043324 Juvenile xanthogranuloma HSDN C2144965 Total blindness in right eye C0271240 Blindness of one eye (disorder) UMLS C3539893 Pelvic pain occurs with intercourse C0205788 Histiocytoid hemangioma HSDN C0007398 Catatonic C0007384 Cataplexy HSDN C4085317 Diarrhea frequency C0043046 Wasting syndrome HSDN C0040264 Ear ringing sound C1334698 Meningothelial cell neoplasm MalaCards C4085642 Level of joint stiffness C3495559 Juvenile arthritis OrphaNet C0004604 Pain back C0001726 Affective symptoms HSDN C0917816 Deficiency mental C1857314 Dermatoleukodystrophy OrphaNet|MalaCards C0009421 Comatose C2827407 Infectious otitis media HSDN C4084784 Diarrhea C0029001 Onchocerciasis HSDN C0018808 Murmur C0006663 Calcinosis HSDN C0036572 Convulsion C0030793 Pelvis tumor HSDN C0427055 Face weakness C0432269 Lenz majewski hyperostotic dwarfism MalaCards C1279888 Proteinuria of undiagnosed cause C0024221 Lymphangioma HSDN C4085317 Diarrhea frequency C0004692 Balantidiasis HSDN C4084724 Usual severity constipation C0033348 Language program HSDN C0000737 Abdomen pain C1334736 Metastatic ovarian small cell carcinoma, hypercalcemic type UMLS C1963093 Dizziness adverse event C0004096 Asthma HSDN C0015672 Decreased energy C0019621 Histiocytosis, langerhans-cell HSDN C0000737 Abdomen pain C0149951 Ovarian fibromata OrphaNet|MalaCards C2024893 Cardiovascular surgery result: fatigue C3808920 Anemia, hypochromic microcytic, with iron overload 2 MalaCards C0013421 Dystonia C0010709 Cyst HSDN C3887873 Hearing loss C0019699 Hiv seropositivity HSDN C0039870 Leanness C0002395 Alzheimer's disease HSDN C0036572 Convulsion C0037933 Spinal diseases HSDN C0005745 Blepharoptosis C1867610 Macrocephaly mesodermal hamartoma spectrum HPO C0036572 Convulsion C0391826 Lhermitte-duclos disease OrphaNet|HPO|MalaCards C4084788 Have dizziness C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0043352 Absent salivary secretion C3276706 Small fiber neuropathy MalaCards C0587050 Lower extremity mass C0740728 Lower extremity problem UMLS C0030554 Abnormal sensation C2932715 Pseudohypoparathyroidism type 1b MalaCards|HPO C0011991 Loose stools C0011303 Demyelinating diseases HSDN C4085211 Pain distress question C0009186 Coccidioidomycosis HSDN C0018808 Murmur C0004096 Asthma HSDN C0009421 Comatose C0221021 Microangiopathic hemolytic anemia MalaCards C0036572 Convulsion C0030421 Paraganglioma HSDN C1963087 Constipation adverse event C0015695 Fatty liver HSDN C0030486 Extremity paralysis, lower C0023895 Liver diseases HSDN C1963177 Muscle pain adverse event C0276386 Mosquito-borne viral fever, oropouche MalaCards C1963281 Vomiting adverse event C0520799 Acute radiation syndrome HSDN C2242996 Tingling C0032965 Pregnancy complications, infectious HSDN C0015230 Exanthem C0157721 Pemphigus, ocular UMLS C0851578 Disorder sleep C2750805 Chromosome 5p13 duplication syndrome MalaCards C2029884 Hearing loss by exam C0850803 Anaphylaxis (non medication) HSDN C0034933 Abnormal reflexes C0040198 Tick toxicoses HSDN C0042571 Vertigo subjective C0149721 Left ventricular hypertrophy HSDN C0241700 Voice fatigue C2931895 Pericardial constriction with growth failure MalaCards C4084774 Have weight loss C0008497 Choriocarcinoma HSDN C0004134 Dyssynergia C0795623 Hepatitis a vaccine, inactivated HSDN C0349588 Stature short C2931047 Hecht scott syndrome OrphaNet C0007859 Pain neck C0752185 Central nervous system helminthiasis HSDN C0454644 Delayed language development C1412746 Bbs1 gene HPO C0021359 Infertility C0342386 Follicle stimulating hormone deficiency MalaCards C0020673 Hypothermia (central) (local) C0004936 Mental disorders HSDN C0149741 Nipple discharge C1332896 Central breast papilloma UMLS C0022107 Fussiness C1857316 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy OrphaNet|HPO C2984058 Have pain C0007894 Cestode infections HSDN C4085211 Pain distress question C0040441 Broken teeth HSDN C2984058 Have pain C0028768 Obsessive-compulsive disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001197 Acrodermatitis HSDN C0242936 Center pain C0206368 Exfoliation syndrome HSDN C0557874 Global developmental delay C2936859 N syndrome OrphaNet|MalaCards C0427068 Legs weakness C2749936 Spastic paraplegia 18, autosomal recessive (disorder) MalaCards|HPO C0007758 Cerebellar ataxia C1963709 Abetalipoproteinemia (lab finding) HSDN C0038990 Sweats C3891556 Chromosome xq26.3 duplication syndrome MalaCards C0030200 Intractable pain C0001726 Affective symptoms HSDN C3898969 Have been vomiting C0027625 Circulating neoplastic cells HSDN C0031911 Pigment deposition C0007099 Carcinoma in situ MalaCards C0234518 Speech slurred C2675211 Episodic ataxia, type 6 (disorder) MalaCards|HPO C1963091 Diarrhea adverse event C0019243 Angioedemas, hereditary HPO C1963170 Hypothermia adverse event C4084909 Depression subordinate domain HSDN C0013604 Edematous C0262655 Recurrent urinary tract infection HSDN C4084766 Vomiting C0969753 Nidovirales infections HSDN C0035232 Diaphragmatic paralysis C0004936 Mental disorders HSDN C0030193 Sense of pain C0028738 Nystagmus HSDN C0030552 Paralysis partial C1852372 Mitochondrial complex iii deficiency (disorder) HPO C0917816 Deficiency mental C0729582 Floating-harbor syndrome OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0031154 Peritonitis HSDN C0037316 Not enough sleeping C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0034150 Skin purpura C0014175 Endometriosis HSDN C0036572 Convulsion C0001584 Adolescent psychology HSDN C0242936 Center pain C0001144 Acne vulgaris HSDN C4084774 Have weight loss C0041582 Ulcer HSDN C0270948 Neurogenic muscular atrophy C3537440 Cystinosis, infantile nephropathic MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0043202 Wolff-parkinson-white syndrome HSDN C1963086 Confusion adverse event C0022336 Creutzfeldt-jakob disease MalaCards|HSDN|HPO C2911647 Weight gain adverse event C0993582 Arthritis, experimental HSDN C0019079 Bloody sputum C3810814 Myocardial infarction ecg assessment HSDN C0016382 Cutaneous vascular engorgement C2186740 Reported urticaria HSDN C0020796 Profoundly mentally retarded C0008626 Congenital chromosomal disease MalaCards C0151740 Intracranial hypertension C0272199 Familial hemophagocytic lymphocytosis MalaCards C3641755 Have constipation C0023743 Linitis plastica HSDN C0007758 Cerebellar ataxia C0013575 Ectodermal dysplasia HSDN C1279888 Proteinuria of undiagnosed cause C0027643 Neoplasm recurrence, local HSDN C0030193 Sense of pain C0020757 Ichthyoses HSDN C0010520 Skin cyanosis C0001127 Acidosis, respiratory HSDN C4085548 Usual severity dizziness C0038019 Spondylosis HSDN C0030193 Sense of pain C0023051 Laryngeal diseases HSDN C4085210 Usual severity pain C1136321 Hiv-associated lipodystrophy syndrome HSDN C2024878 Cardiovascular surgery result: dyspnea C0018923 Hemangiosarcoma HSDN C0016199 Pain flank C0035358 Retroperitoneal neoplasm HSDN C1557397 Adverse event associated with pain C0022667 Papillary necrosis HSDN C1963281 Vomiting adverse event C0405580 Adrenal cortical hypofunction HSDN C0917801 Sleep disorder insomnia C4274503 Insomnia co-occurrent and due to nocturnal myoclonus UMLS C0007758 Cerebellar ataxia C2931092 Maternally inherited leigh syndrome MalaCards C0013911 Emaciate C0027804 Fatigue neurosis HSDN C1961131 Cough adverse event C1963064 Anxiety adverse event HSDN C0007758 Cerebellar ataxia C0016154 Fish disease HSDN C0085128 Cardiac output elevated C0036992 Short bowel syndrome HSDN C0027066 Myoclonic jerking C0751955 Brain infarction HSDN C0030486 Extremity paralysis, lower C1623041 Breast-fed HSDN C1253937 Pericardial effusion C0343206 Hypocomplementemic urticarial vasculitis MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0040765 Transsexualism HSDN C4020887 Photodysphoria C0024198 Lyme disease MalaCards C4084784 Diarrhea C0016053 Fibromyalgia HSDN C1971624 Appetite absent C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0004134 Dyssynergia C0035801 Diseases rodent HSDN C3274924 Have been coughing C0021845 Intestinal perforation HSDN C0000737 Abdomen pain C0085207 Gestational diabetes HSDN C4084775 Usual severity weight loss C0263311 Senile dermatitis herpetiform MalaCards C0002965 Crescendo angina C1253943 Fluid in the chest HSDN C4084775 Usual severity weight loss C0342273 Transient neonatal diabetes mellitus MalaCards C0242936 Center pain C0027438 Nasopharynx HSDN C0019079 Bloody sputum C0862780 Stage iiib adenosquamous cell carcinoma of lung UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0042076 Urologic neoplasms HSDN C2237041 Shox gene with short stature C3281084 Congenital disorder of glycosylation, type ir MalaCards C2237041 Shox gene with short stature C0729582 Floating-harbor syndrome OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0007781 Intracranial embolism and thrombosis HSDN C0042025 Urinary incontinence stress C0041974 Urethral stricture HSDN C0027796 Neuralgias C4085311 Depression - recess HSDN C4084726 Distress cough C3539920 Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive MalaCards C0020903 Illusion C0497327 Dementia HSDN C0015970 Fever unknown origin C0005943 Bone diseases infectious HSDN C4084727 Cough frequency C0017416 Genital neoplasms, female HSDN C4084768 Usual severity vomiting C2706915 Language:-:point in time:^patient:- HSDN C2029884 Hearing loss by exam C0024761 Communication, manual HSDN C1963071 Back pain adverse event C0003838 Arterial occlusive diseases HSDN C0086565 Liver function abnormal C2609268 Low phospholipid-associated cholelithiasis MalaCards C0020538 Hbp C1859783 Angiomatosis, diffuse corticomeningeal, of divry and van bogaert MalaCards C0007814 Cerebrospinal fluid otorrhea C0003803 Arnold chiari malformation HSDN C3815497 Cough C1963064 Anxiety adverse event HSDN C1557397 Adverse event associated with pain C0037054 Sickle cell trait MalaCards|HSDN C0018681 Headache, cephalalgia C0271051 Macular retinal edema HSDN C4085210 Usual severity pain C0869332 Of water deprivation HSDN C0349588 Stature short C2931050 Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies OrphaNet C0232493 Epigastric pain C0030920 Peptic ulcer UMLS C0042514 Ventricular tachycardia C1832680 Cardiomyopathy, dilated, 1e MalaCards C0010200 Cough symptom C0030424 Paragonimiasis HSDN C0013132 Drooling C0796204 Worster-drought syndrome MalaCards C0857305 Thrombocytopenia purpura C0031117 Peripheral neuropathy HSDN C0041834 Erythematous condition C0030328 Panniculitis, nodular nonsuppurative OrphaNet|MalaCards C2242996 Tingling C2932715 Pseudohypoparathyroidism type 1b MalaCards|HPO C1963063 Anorexia adverse event C0038661 Suicide HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0018021 Goiter HSDN C0003467 Angst C0162532 Variegate porphyria MalaCards|HPO C2984058 Have pain C0018920 Hemangioma, cavernous HSDN C1279888 Proteinuria of undiagnosed cause C0005396 Bile duct neoplasms HSDN C4085862 Bothered by nausea C1385938 Acanthocephaliasis MalaCards C3641755 Have constipation C0700208 Acquired scoliosis HSDN C0018772 Deafness C1849112 Spastic quadriplegia-retinitis pigmentosa-mental retardation syndrome MalaCards C0038506 Stutter C0033903 Psychologic technic HSDN C0011991 Loose stools C0018199 Granuloma, plasma cell HSDN C3539889 Pelvic pain increasing in severity C0206767 Neoplasms, cystic, mucinous, and serous HSDN C4050613 Anxiety C0031485 Phenylketonurias MalaCards C0018965 Blood urine C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C1963184 Nystagmus adverse event C1856689 Friedreich ataxia 1 HPO C4084788 Have dizziness C0002395 Alzheimer's disease HSDN C0155552 Hearing loss mixed C0023702 Injury lightning HSDN C0013421 Dystonia C1858391 Ataxia-telangiectasia-like disorder HPO C0020580 Decreased sensation C0002173 Follicular mucinosis HSDN C3829611 Nausea frequency C0018794 Heart block HSDN C0019559 Hip arthralgia C3715079 Developmental dysplasia of the hip 2 UMLS C4042891 Sleep wake disorders C0027743 Nerve compression syndrome HSDN C0007859 Pain neck C0034065 Pulmonary embolism HSDN C0004134 Dyssynergia C0155338 Total ophthalmoplegia MalaCards C2984057 Have nausea C1000587 Pemphigus HSDN C4085210 Usual severity pain C0024205 Lymphadenitis HSDN C0013421 Dystonia C0031485 Phenylketonurias HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C2239176 Liver carcinoma HSDN C0878773 Bladder hyperactive C0016658 Fracture bone HSDN C3641755 Have constipation C0021368 Inflammation HSDN C0030486 Extremity paralysis, lower C2984291 Glioblastoma multiforme pathway HSDN C1384666 Decreased hearing C1838162 Mesomelia-synostoses syndrome MalaCards C0518090 Frequency of pain question C0023348 Leprosy, lepromatous HSDN C2315100 Pediatric failure to thrive C0007222 Cardiovascular diseases HSDN C0030193 Sense of pain C0042266 Vaginismus HSDN C0860603 Anxiety symptom C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0039870 Leanness C0008073 Developmental disabilities HSDN C2362324 Pediatric obesity C0016724 Froehlich's syndrome HSDN C1384666 Decreased hearing C2936502 Charge syndrome, familial MalaCards C4084768 Usual severity vomiting C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C4084768 Usual severity vomiting C0033860 Psoriasis HSDN C0030193 Sense of pain C0013449 Ear neoplasms HSDN C0011570 Monopolar depression C2931205 Usher syndrome, type 1a MalaCards C0003862 Pain joint C1956346 Coronary artery disease HSDN C1549543 Administration method - pain C0014805 Primary erythermalgia HPO C0028738 Nystagmus C1327919 Myelocerebellar disorder OrphaNet|HPO C0332563 Papulae C0268397 Amyloidosis, primary cutaneous MalaCards C0011168 Disorder deglutition C1835664 Tylosis with esophageal cancer MalaCards C0033774 Skin pruritus C0022658 Kidney diseases HSDN C4085211 Pain distress question C0001427 Adenoiditis, nos MalaCards C4084726 Distress cough C1258104 Diffuse scleroderma HSDN C0235267 Eye redness C0343633 Brazilian haemorrhagic fever MalaCards C0013362 Dysarthrias C0023522 Leukodystrophy, metachromatic MalaCards|HSDN|HPO C3274924 Have been coughing C0872315 Communicable diseases emerging HSDN C0005779 Clotting C0346109 Malignant mesothelioma of peritoneum MalaCards C0034933 Abnormal reflexes C0017181 Gastrointestinal hemorrhage HSDN C1963252 Tremor adverse event C0033941 Psychoses, substance-induced HSDN C0008031 Pain chest C3494506 Pseudohypoparathyroidism, type ia HPO C0151786 Weakness muscle C2752015 Glycogen storage disease xiv MalaCards|UMLS C0042963 Symptoms vomiting C0342869 Deficiency of acetyl-coa acyltransferase (disorder) MalaCards C4084727 Cough frequency C0036864 Sexual relations HSDN C4085317 Diarrhea frequency C0004442 Avoidance learning HSDN C4085211 Pain distress question C0269185 Uterus retroverted HSDN C3274924 Have been coughing C0010346 Crohn disease HSDN C4084727 Cough frequency C0008924 Cleft lip HSDN C0004604 Pain back C0517555 Venous thrombosis after immobility HSDN C2029884 Hearing loss by exam C0853697 Neutrophil count decreased HSDN C0018775 Hearing loss bilateral C0524812 Intracranial hypotension HSDN C1565249 Limitation, mobility C0008525 Choroideremia HSDN C0497406 Over weight C0023223 Leg ulcer HSDN C0036572 Convulsion C0027404 Narcolepsy HSDN C2242996 Tingling C0078981 Arachnoid cysts HSDN C0041834 Erythematous condition C0406756 Keratolytic winter erythema OrphaNet|MalaCards C0042571 Vertigo subjective C0518449 Control of hip fracture risk HSDN C0036572 Convulsion C0206083 Myelinoclasis, central pontine HSDN C0018772 Deafness C0023176 Lead poisoning HSDN C1997249 Neuralgia, pudendal C0080179 Vertebra fracture HSDN C0002962 Angina C0043065 Water electrolyte imbalance HSDN C0013421 Dystonia C0268247 Niemann-pick disease, type d MalaCards|HPO C0004134 Dyssynergia C3151343 Spinocerebellar ataxia 32 MalaCards C0239181 Diarrhea intermittent C2931296 Yorifuji okuno syndrome OrphaNet|HPO C0004604 Pain back C0085580 Essential hypertension UMLS C0020538 Hbp C0950122 Frasier syndrome MalaCards C0233565 Bradykinesia C1853578 Neuroferritinopathy OrphaNet|UMLS|HPO|MalaCards C1961131 Cough adverse event C0264303 Laryngomalacia HSDN C2203646 Jaundice C0009375 Colonic neoplasms HSDN C0036572 Convulsion C0270820 Gelastic epilepsy UMLS C0015672 Decreased energy C0206255 Malaria vaccine HSDN C0231528 Muscle pain generalized C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0700590 Diaphoresis excessive C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C0030193 Sense of pain C0001768 Agammaglobulinemia HSDN C0277959 Hair coarseness C3554774 Tyshchenko syndrome MalaCards C3539892 Pelvic pain in front C0023467 Leukemia, myelocytic, acute HSDN C0018681 Headache, cephalalgia C0011616 Contact dermatitis HSDN C0151889 Reflexes tendon increased C1838577 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy HPO C0018681 Headache, cephalalgia C0039726 Disease, thalamic HSDN C3665347 Vision impaired C0268506 Albinoidism MalaCards C0043094 Weight gain C0008625 Chromosome aberrations HSDN C0231218 Malaise generalized C1333307 Adenocarcinoma of distal 1/3 of common bile duct UMLS C3539020 Pelvic pain decreasing in frequency C1962963 Osteoporosis adverse event HSDN C0857305 Thrombocytopenia purpura C0004238 Atrial fibrillation HSDN C0028738 Nystagmus C2678263 Methylmalonic acidemia, cblh type, formerly HPO C1000483 Genus anemia C1291329 Transaldolase deficiency OrphaNet|HPO|MalaCards C0036572 Convulsion C0022408 Arthropathy HSDN C1971624 Appetite absent C0019159 Hepatitis a DiseaseOntology|MalaCards C4085210 Usual severity pain C0014118 Endocarditis HSDN C0015468 Face pain C0035229 Respiratory insufficiency HSDN C0000737 Abdomen pain C0013370 Amebic colitis HSDN C3898969 Have been vomiting C0027663 Neoplasms, multiple primary HSDN C4084769 Vomiting frequency C1456865 Ureteral calculi HSDN C0010200 Cough symptom C0810299 Other and unspecified lower respiratory disease UMLS C0015970 Fever unknown origin C0268412 Infantile hypophosphatasia UMLS C0036572 Convulsion C0585274 Periodic syndrome OrphaNet|HPO C0042963 Symptoms vomiting C0032319 Pneumopericardium HSDN C0576456 Poor feeding C3809875 Van maldergem syndrome 2 MalaCards C0036572 Convulsion C0026782 Mumps vaccine HSDN C0857174 Pink macular rash on exposed areas C0162830 Dermatitis, phototoxic UMLS C0237326 Defecation pain C3854315 Pseudoprimary hyperaldosteronism MalaCards C2911647 Weight gain adverse event C0003864 Arthritis HSDN C0086565 Liver function abnormal C3150672 Arthrogryposis, renal dysfunction, and cholestasis 2 MalaCards|HPO C0004604 Pain back C0006145 Breast diseases HSDN C0033377 Caudal displacement C0026896 Myasthenia gravis OrphaNet|MalaCards C4084802 Usual severity diarrhea C0006818 Campylobacter infection DiseaseOntology C4085661 Usual severity nausea C0030807 Pemphigus, nos HSDN C0004134 Dyssynergia C2677792 Riddle syndrome MalaCards|HPO|UMLS C0004134 Dyssynergia C0020757 Ichthyoses HSDN C0011991 Loose stools C0038436 Post-traumatic stress disorder HSDN C1838869 Proximal neurogenic muscle weakness C1861451 Stormorken syndrome MalaCards C4084775 Usual severity weight loss C0037397 Behavior social HSDN C0005745 Blepharoptosis C3810265 Warburg micro syndrome 4 MalaCards C0000737 Abdomen pain C0268553 Hyperlysinemias HSDN C1963086 Confusion adverse event C0020635 Hypopituitarism HSDN C0030552 Paralysis partial C0007760 Cerebellar diseases HSDN C1963091 Diarrhea adverse event C0037051 Behavior illness HSDN C0030552 Paralysis partial C0003855 Arteriovenous fistula HSDN C0018772 Deafness C0024305 Lymphoma, non-hodgkin HSDN C0002965 Crescendo angina C0002871 Anemia HSDN C3641756 Have diarrhea C0014457 Eosinophilia HSDN C4085862 Bothered by nausea C0040479 Torsades de pointes HSDN C0005779 Clotting C1848213 Periventricular heterotopia, x-linked HPO C0013404 Respiratory difficulty C0518449 Control of hip fracture risk HSDN C0040822 D tremors C0524851 Neurodegenerative disorders HSDN C1962972 Proteinuria adverse event C1963119 Stomach ulcer adverse event HSDN C1961131 Cough adverse event C0040583 Tracheal stenosis HSDN C1963091 Diarrhea adverse event C0149514 Bronchitis acute HSDN C4084768 Usual severity vomiting C2239176 Liver carcinoma HSDN C0029163 Hemorrhage mouth C0007222 Cardiovascular diseases HSDN C0427055 Face weakness C3553538 Brown-vialetto-van laere syndrome 2 MalaCards|UMLS C3539889 Pelvic pain increasing in severity C0042253 Vaginal fistula HSDN C1553188 Hemolysis - observation C0002895 Anemia, sickle cell MalaCards C0011570 Monopolar depression C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C2911647 Weight gain adverse event C0011848 Diabetes insipidus HSDN C0019209 Large liver C3553937 Pbd4b MalaCards C4085317 Diarrhea frequency C0687720 Central diabetes insipidus MalaCards C3641756 Have diarrhea C0034494 Rabies (disorder) OrphaNet|HSDN|MalaCards C0042571 Vertigo subjective C0035078 Kidney failure HSDN C1963167 Memory impairment adverse event C0376329 New variant creutzfeldt-jakob disease MalaCards|HPO C0427190 Ataxia, truncal C1853761 Spinocerebellar ataxia, autosomal recessive 1 MalaCards C1961131 Cough adverse event C0011854 Diabetes mellitus, insulin-dependent HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0236964 Attention deficit and disruptive behavior disorders HSDN C0019209 Large liver C1412573 Asah1 gene HPO C2024878 Cardiovascular surgery result: dyspnea C0265908 Congenital atresia of pulmonary artery HSDN C0009421 Comatose C3665624 Serum calcium below normal HSDN C1963249 Tinnitus adverse event C0563150 Catastrophization HSDN C2984057 Have nausea C3554462 Mitochondrial dna depletion syndrome 11 MalaCards C0242936 Center pain C0025063 Mediastinal neoplasms HSDN C0027497 Queasy C0020542 Pulmonary hypertension HSDN C0009421 Comatose C2984289 Melanoma pathway HSDN C0232466 Feeding difficulty C0023944 Cerebromedullospinal disconnection OrphaNet|MalaCards C1963071 Back pain adverse event C1264008 Chronic cold agglutinin disease MalaCards C0030554 Abnormal sensation C0021432 Infratentorial neoplasms HSDN C0242936 Center pain C0022367 Jaw, edentulous, partially HSDN C4085210 Usual severity pain C0010414 Infection by cryptococcus neoformans HSDN C0036572 Convulsion C1332612 Brain stem intraparenchymal clear cell meningioma UMLS C0018834 Brash C0265246 Townes syndrome HPO C4084774 Have weight loss C0010054 Coronary arteriosclerosis HSDN C0234146 Absent reflex C1970011 Charcot-marie-tooth disease, type 4j MalaCards|HPO C3641755 Have constipation C0019196 Hepatitis c HSDN C3665492 Pigmentations C1302853 Squamous cell carcinoma - category MalaCards C0151889 Reflexes tendon increased C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C3898969 Have been vomiting C0342870 Bifunctional peroxisomal enzyme deficiency MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0018188 Granuloma HSDN C3539895 Pelvic pain occurs with bowel movement C0015732 Fecal incontinence HSDN C4084723 Constipation C0023343 Leprosy HSDN C0040264 Ear ringing sound C1834580 Myoclonus and ataxia MalaCards C0085636 Light sensitivity C4041558 Cone-rod synaptic disorder, congenital nonprogressive MalaCards|UMLS C2315100 Pediatric failure to thrive C0270972 Cornelia de lange syndrome OrphaNet|HSDN|HPO|MalaCards C2919142 Short stature adverse event C3150942 Spondylocostal dysostosis 4, autosomal recessive MalaCards|HPO C4085211 Pain distress question C0376547 Aromatherapy HSDN C0019209 Large liver C4014605 Polyglucosan body myopathy 1 with or without immunodeficiency MalaCards C3815497 Cough C0019284 Diaphragmatic hernia HSDN C1963281 Vomiting adverse event C0023890 Liver cirrhosis HSDN C2984058 Have pain C0042345 Varicosity HSDN C4085210 Usual severity pain C0007177 Cardiac tamponade HSDN C0013604 Edematous C0272295 Purpura, rheumatica MalaCards C3539892 Pelvic pain in front C0242669 Placenta retained HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0270327 Bedwetting HSDN C0035229 Respiratory function impaired C0795933 Edinburgh malformation syndrome OrphaNet|MalaCards C0917816 Deficiency mental C0796081 Growth mental deficiency syndrome of myhre MalaCards|HPO C0000737 Abdomen pain C1556682 Adverse event associated with infection HSDN C2984058 Have pain C0013364 Dysautonomia, familial HSDN C0018784 Deafness sensorineural C0013010 Cerebral lateralization HSDN C4084769 Vomiting frequency C0262584 Carcinoma, small cell HSDN C3827868 Tachycardia by ecg finding C0031511 Pheochromocytoma MalaCards|HPO C0973461 Dysphasia C2746066 Combined d-2- and l-2-hydroxyglutaric aciduria MalaCards C0018772 Deafness C0023343 Leprosy HSDN C4085222 Nausea C3489393 Hiatal hernia HSDN C1279888 Proteinuria of undiagnosed cause C0024299 Lymphoma HSDN C3539891 Pelvic pain to the rear C0001261 Actinomycosis HSDN C2911647 Weight gain adverse event C0025205 Melanoma, experimental HSDN C0019825 Voice hoarseness C0221759 Brachial plexus neuritis HSDN C0036572 Convulsion C0032227 Pleural effusion disorder HSDN C0020538 Hbp C2677362 Alveolar capillary dysplasia MalaCards C0022346 Yellow skin C0162510 Caroli disease HSDN C0018681 Headache, cephalalgia C0079487 Helicobacter infections HSDN C4084774 Have weight loss C0038525 Subarachnoid hemorrhage HSDN C1962972 Proteinuria adverse event C0026691 Mucocutaneous lymph node syndrome OrphaNet|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0029882 Otitis media HSDN C1961131 Cough adverse event C3540844 Ciliary dyskinesia, primary, 20 MalaCards C4084802 Usual severity diarrhea C0597109 Nurse's role HSDN C1549543 Administration method - pain C0007527 Cecal disease HSDN C0003862 Pain joint C0035920 Rubella DiseaseOntology|MalaCards C4042891 Sleep wake disorders C0037274 Dermatologic disorders HSDN C0042963 Symptoms vomiting C0524909 Hepatitis b, chronic MalaCards C2700617 Irritation - emotion C3494506 Pseudohypoparathyroidism, type ia HPO C0007758 Cerebellar ataxia C0078981 Arachnoid cysts HSDN C1963137 Hydrocephalus adverse event C2931197 Waaler aarskog syndrome MalaCards C0242936 Center pain C0011603 Dermatitis HSDN C0518090 Frequency of pain question C0021432 Infratentorial neoplasms HSDN C3641755 Have constipation C0037650 Somatoform disorder HSDN C4084767 Bothered by vomiting C0006663 Calcinosis HSDN C3539022 Pelvic pain decreasing in severity C0302148 Blood clot HSDN C3665492 Pigmentations C1336905 Endometrial endometrioid adenocarcinoma MalaCards C3641756 Have diarrhea C0023869 Lithiasis HSDN C2919142 Short stature adverse event C0265326 Bannayan-riley-ruvalcaba syndrome OrphaNet|HPO|MalaCards C0747556 Pharyngitis recurrent C0013575 Ectodermal dysplasia MalaCards C4084802 Usual severity diarrhea C0027794 Neural tube defects HSDN C0018777 Deafness, conductive C0265233 Cryptophthalmos syndrome HPO C4085211 Pain distress question C0017510 Gestures HSDN C2919142 Short stature adverse event C0268292 Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency OrphaNet|HPO C0030193 Sense of pain C0085392 Bacteroidaceae infection HSDN C3274924 Have been coughing C0018193 Granuloma, foreign-body HSDN C0917816 Deficiency mental C1860471 Stoll alembik dott syndrome MalaCards C0018991 Paralysis one side of body C0024305 Lymphoma, non-hodgkin HSDN C0033774 Skin pruritus C0861854 Adenosquamous bile duct carcinoma UMLS C4085211 Pain distress question C2186740 Reported urticaria HSDN C0042571 Vertigo subjective C0029883 Otitis media with effusion HSDN C0016204 Fart C0034183 Pyelitis unspecified HSDN C1963067 Atrial fibrillation adverse event C3151204 Cardiomyopathy, familial hypertrophic, 16 HPO C0085631 Abnormal excitement C0041296 Tuberculosis HSDN C0019209 Large liver C1333764 Gastric cronkhite canada polyposis MalaCards C0036572 Convulsion C0034040 Puerperal disorders HSDN C0040822 D tremors C1837396 Congenital disorder of glycosylation, type ie MalaCards|HPO|UMLS C0036572 Convulsion C0026896 Myasthenia gravis MalaCards|HSDN C0007758 Cerebellar ataxia C0037929 Spinal cord injuries HSDN C0242936 Center pain C0085096 Peripheral vascular diseases HSDN C0270846 Astatic seizure C4015395 Generalized epilepsy with febrile seizures plus, type 9 MalaCards C2237041 Shox gene with short stature C2936861 Cortisol 11-beta-ketoreductase deficiency MalaCards C1963137 Hydrocephalus adverse event C0220659 Acrodysostosis HPO C2362324 Pediatric obesity C0004903 Beckwith-wiedemann syndrome HSDN C0917816 Deficiency mental C0796083 Najjar syndrome HPO C0035232 Diaphragmatic paralysis C0018802 Congestive heart failure HSDN C0036572 Convulsion C1865323 Migraine, familial basilar HPO C2096293 Ent surgical result ear vertigo C0020502 Hyperparathyroidism HSDN C0085631 Abnormal excitement C0236642 Pick disease of the brain HSDN C0018965 Blood urine C0263591 Lupus erythematosus drug induced MalaCards C3665492 Pigmentations C1266158 Nonseminomatous germ cell tumor MalaCards C0027498 Nausea vomiting C0153463 Malig neop oth spec pancreas MalaCards C4084723 Constipation C0024115 Lung diseases HSDN C4084776 Weight loss C0043124 West nile fever HSDN C0035455 Rhinitis C3809701 Ciliary dyskinesia, primary, 27 MalaCards C3539892 Pelvic pain in front C0009375 Colonic neoplasms HSDN C4084788 Have dizziness C1956346 Coronary artery disease HSDN C0878773 Bladder hyperactive C3810814 Myocardial infarction ecg assessment HSDN C0026821 Cramp C2706915 Language:-:point in time:^patient:- HSDN C4084784 Diarrhea C0162872 Aortic aneurysm, thoracic HSDN C0023015 Language handicap C1999266 Depression adverse event HSDN C0424755 Fever symptoms C0086438 Hypogammaglobulinemia OrphaNet|MalaCards C1963252 Tremor adverse event C0016542 Foreign body HSDN C4084769 Vomiting frequency C0030354 Papilloma HSDN C0013390 Cramps menstrual C0014544 Epilepsy HSDN C3539893 Pelvic pain occurs with intercourse C1881674 Medical device emits smoke HSDN C0028738 Nystagmus C0003803 Arnold chiari malformation MalaCards C0242936 Center pain C0021833 Intestinal fistula HSDN C3665492 Pigmentations C3495438 Macular degeneration, age-related, 2 MalaCards C0018772 Deafness C0001624 Adrenal gland neoplasms HSDN C0035078 Failure kidney C0016952 Galactosemias MalaCards C0013604 Edematous C2219717 Menstrual periods stopped for over 6 months HSDN C0007758 Cerebellar ataxia C0270724 Infantile neuroaxonal dystrophy HPO C1963281 Vomiting adverse event C0018923 Hemangiosarcoma HSDN C0012833 Dizzy C1701938 Associated pulmonary arterial hypertension OrphaNet C2911647 Weight gain adverse event C0015663 Fasting HSDN C0027796 Neuralgias C0021831 Intestinal diseases HSDN C1963281 Vomiting adverse event C0029456 Osteoporosis HSDN C4084773 Bothered by weight gain C0035369 Retroviridae infections HSDN C2188545 Anuria C2678367 Renal tubular dysgenesis with choanal atresia and athelia HPO C4084802 Usual severity diarrhea C1306794 Wound botulism MalaCards C1963087 Constipation adverse event C0033247 Proctocolitis HSDN C3898969 Have been vomiting C0008626 Congenital chromosomal disease HSDN C4084768 Usual severity vomiting C0043168 Whooping cough due to unspecified organism HSDN C0019079 Bloody sputum C0220847 C hepatitis virus HSDN C0743973 Fever high C0040584 Tracheitis DiseaseOntology C0010200 Cough symptom C0008325 Cholecystitis HSDN C0010200 Cough symptom C1710174 Squamous cell lung carcinoma, clear cell variant UMLS C0008031 Pain chest C0206369 Splenosis HSDN C2911647 Weight gain adverse event C1961102 Precursor cell lymphoblastic leukemia lymphoma HSDN C2984058 Have pain C0011649 Dermoid cyst HSDN C0019572 Hairiness C0221032 Familial generalized lipodystrophy MalaCards|HSDN C4084784 Diarrhea C0015652 Fascioliasis HSDN C0522224 Palsied C0042510 Ventricular fibrillation HSDN C0030200 Intractable pain C0033348 Language program HSDN C0241157 Skin pustule C0014522 Epidermodysplasia verruciformis OrphaNet|HPO|MalaCards C0234518 Speech slurred C2931859 Acquired cjd MalaCards C0518090 Frequency of pain question C0282504 Environmental allergies HSDN C4085642 Level of joint stiffness C0265309 Leri-weill dyschondrosteosis OrphaNet|HPO|MalaCards C3539892 Pelvic pain in front C0037072 Diseases sigmoid HSDN C0013395 Indigestion C0021400 Influenza HSDN C0026838 Spasticity muscle C0013592 Ectropion HSDN C0035229 Respiratory function impaired C0043459 Zellweger syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0019562 Von hippel-lindau syndrome HSDN C3541349 Syncope C0340493 Paroxysmal familial ventricular fibrillation MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0036875 Disorders of sex development HSDN C3539889 Pelvic pain increasing in severity C0272414 Displaced spleen HSDN C0030552 Paralysis partial C0020523 Immediate hypersensitivity HSDN C1963091 Diarrhea adverse event C0206624 Hepatoblastoma MalaCards C0018784 Deafness sensorineural C1852510 Craniofacial deafness hand syndrome OrphaNet|HPO|MalaCards C0031154 Peritonitis, nos C1882229 Ovarian thecoma MalaCards C1557397 Adverse event associated with pain C0033075 Presbyopia HSDN C4085549 Dizziness C0018801 Heart failure HSDN C0042024 Urine incontinence C0007787 Transient ischemic attack HSDN C4084769 Vomiting frequency C1855371 Maple syrup urine disease, type ii HPO C0030554 Abnormal sensation C0022367 Jaw, edentulous, partially HSDN C0727671 Red cross toothache drops C0234194 Nociception HSDN C4084773 Bothered by weight gain C1145628 Autonomic nervous system disorders HSDN C0424755 Fever symptoms C0016978 Gallbladder neoplasm HSDN C0520909 Ponv C0376298 Consensus HSDN C1549543 Administration method - pain C0009442 Common bile duct neoplasms HSDN C4084725 Usual severity cough C0019337 Heroin dependence HSDN C0234146 Absent reflex C2931022 Amyloidosis, cerebral, with spongiform encephalopathy MalaCards C4085548 Usual severity dizziness C0001807 Aggressive behavior HSDN C2237041 Shox gene with short stature C1275081 Cardio-facio-cutaneous syndrome OrphaNet|HPO C4085211 Pain distress question C0016470 Food allergy HSDN C0231791 In toe C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards C0151311 Cranial nerve palsy C0006035 Borrelia infections MalaCards C0009421 Comatose C0001125 Acidosis, lactic HSDN C4085317 Diarrhea frequency C0039483 Giant cell arteritis HSDN C4084784 Diarrhea C1963211 Pericarditis adverse event HSDN C0019825 Voice hoarseness C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C2024893 Cardiovascular surgery result: fatigue C0038354 Stomach diseases HSDN C0700590 Diaphoresis excessive C1858517 Spinal muscular atrophy with respiratory distress 1 HPO C4084788 Have dizziness C0040046 Thrombophlebitis HSDN C4085211 Pain distress question C0206694 Mucoepidermoid carcinoma HSDN C0031911 Pigment deposition C0751593 Cancer, infratentorial MalaCards C0242936 Center pain C0034091 Pulmonary veno-occlusive disease (disorder) HSDN C0028738 Nystagmus C1860860 Neuhauser daly magnelli syndrome MalaCards C0018989 Paresis of one side of body C1838122 Arterial dissection with lentiginosis OrphaNet|MalaCards C1000483 Genus anemia C0043194 Wiskott-aldrich syndrome OrphaNet|MalaCards C3898969 Have been vomiting C0518449 Control of hip fracture risk HSDN C0917816 Deficiency mental C0268138 Xeroderma pigmentosum, complementation group d HPO C1549543 Administration method - pain C0020497 Cortical congenital hyperostosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0033324 Prognathism HSDN C0575081 Abnormal gait C1842675 Amyotrophic lateral sclerosis 6 (disorder) HPO C4084767 Bothered by vomiting C0342873 Glutaric aciduria iii MalaCards|HPO C0037763 Spasm C0042138 Uterine neoplasms HSDN C0034150 Skin purpura C0023530 Leukopenia HSDN C0002962 Angina C0034362 Q fever HSDN C0518090 Frequency of pain question C0030569 Secondary parkinson disease HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0008049 Chicken pox DiseaseOntology|HSDN|MalaCards C3146279 Coma C0004114 Astrocytoma HSDN C4085210 Usual severity pain C0008475 Patella chondromalacia HSDN C1962972 Proteinuria adverse event C4049994 Insulin resistance measurement HSDN C4084776 Weight loss C0023220 Leg injury HSDN C1963087 Constipation adverse event C0007194 Hypertrophic cardiomyopathy HSDN C0042024 Urine incontinence C0010674 Cystic fibrosis HSDN C0232466 Feeding difficulty C3809877 Schaaf-yang syndrome MalaCards C4085210 Usual severity pain C0162532 Variegate porphyria MalaCards C0234518 Speech slurred C0431401 Gillespie syndrome MalaCards C0030193 Sense of pain C0037356 Smallpox virus HSDN C1549543 Administration method - pain C0029899 Otosclerosis HSDN C2242996 Tingling C0271972 Thiamine-responsive megaloblastic anemia MalaCards C0017565 Gingiva hemorrhage C2584774 Congenital hypofibrinogenemia OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0948039 Bacterial gastritis MalaCards C4084788 Have dizziness C2936631 Complaint, subjective health HSDN C0162298 Stiffness joints C0220726 Diastrophic dysplasia OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0162790 Harassment sexual HSDN C0010520 Skin cyanosis C1548777 Specimen reject reason - hemolysis HSDN C0006370 Bulimia C0010674 Cystic fibrosis HSDN C0020450 Hyperemesis gravidarum C0027651 Tumor HSDN C4084767 Bothered by vomiting C0026850 Muscular dystrophy HSDN C1963154 Renal failure adverse event C0019101 Hemorrhagic fever with renal syndrome DiseaseOntology|MalaCards C2096293 Ent surgical result ear vertigo C1836545 Alpha-n-acetylgalactosaminidase deficiency, type iii MalaCards C0242936 Center pain C0006736 Body stone HSDN C0521635 Female genital leucoplakia C0410013 Soft tissue lesion UMLS C4084774 Have weight loss C0878675 Erdheim-chester disease OrphaNet|HSDN|MalaCards C0009806 Constipate C0300948 Caudal regression syndrome HPO C0020580 Decreased sensation C0008728 Churg-strauss syndrome HSDN C0151786 Weakness muscle C0040136 Thyroid neoplasm HSDN C2984058 Have pain C0001957 Alcohol withdrawal delirium HSDN C0038990 Sweats C0007279 Carotid body paraganglioma HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0003175 Anthrax disease HSDN C3146279 Coma C0011881 Diabetic nephropathy HSDN C0150055 Pain chronic C0007097 Carcinomas HSDN C1963091 Diarrhea adverse event C0039590 Testicular neoplasms HSDN C4084767 Bothered by vomiting C1704272 Benign prostatic hyperplasia HSDN C0155552 Hearing loss mixed C2936502 Charge syndrome, familial MalaCards C0025323 Bleeding menstrual heavy C1264041 Von willebrand disease, type 3 HPO C0010200 Cough symptom C0343528 Legionella pneumophila; infection, nonpneumonic OrphaNet|MalaCards C0040264 Ear ringing sound C1568248 Usher syndrome, type iii MalaCards C0042928 Paralysis vocal cord C0003486 Aortic aneurysm HSDN C1557397 Adverse event associated with pain C0002351 Altitude sickness HSDN C0018524 Hallucinate C0006309 Brucellosis HSDN C0009806 Constipate C0023895 Liver diseases HSDN C0015469 Facial paralysis C0042164 Uveitis HSDN C0852979 Coma nec C0009421 Comatose UMLS C1962972 Proteinuria adverse event C0023267 Fibroid tumor HSDN C1384666 Decreased hearing C1836929 Emanuel syndrome OrphaNet|MalaCards C0030554 Abnormal sensation C0936215 Vitamin b 6 deficiency HSDN C0036572 Convulsion C1838281 Fryns macrocephaly OrphaNet|UMLS|MalaCards C0028738 Nystagmus C1839780 Fragile x tremor/ataxia syndrome MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0206660 Germinoma HSDN C0011991 Loose stools C0746781 Nausea intractable UMLS C1069915 Vertigo C3163620 Hypotension adverse event HSDN C0026838 Spasticity muscle C1860808 Triosephosphate isomerase deficiency UMLS C0040485 Wryneck C1836756 Arthrogryposis, distal, type 4 (disorder) MalaCards C1000483 Genus anemia C2931618 Gestational trophoblastic disease MalaCards C0036572 Convulsion C0018021 Goiter HSDN C3463815 Feel fatigue C0036341 Schizophrenia HSDN C0427055 Face weakness C4225405 Myasthenic syndrome, congenital, 1b, fast-channel UMLS C0497247 Blood pressure elevation C1510460 Orofaciodigital syndrome i MalaCards|HPO C0036572 Convulsion C4015357 Mental retardation, autosomal dominant 31 MalaCards|UMLS C1963064 Anxiety adverse event C0002875 Cooley's anemia OrphaNet|HPO C0424755 Fever symptoms C0038041 Spotted fevers DiseaseOntology|MalaCards C0349588 Stature short C1563720 Kallmann syndrome 2 (disorder) MalaCards|HPO C4084766 Vomiting C0162871 Aortic aneurysm, abdominal HSDN C0036572 Convulsion C3891556 Chromosome xq26.3 duplication syndrome MalaCards C3463815 Feel fatigue C0019542 Higher nervous activity HSDN C0004134 Dyssynergia C0011570 Mental depression HSDN C0518090 Frequency of pain question C0149678 Epstein-barr virus infections HSDN C0085593 Chill C0030319 Panic disorder HSDN C4084788 Have dizziness C0029132 Disorder of the optic nerve HSDN C0036572 Convulsion C0017531 Angiolymphoid hyperplasia HSDN C0007758 Cerebellar ataxia C0391826 Lhermitte-duclos disease OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C1832386 Diabetes mellitus, transient neonatal, 1 OrphaNet|HPO|MalaCards C0332563 Papulae C1833030 Palmoplantar keratoderma, nonepidermolytic OrphaNet|HPO|MalaCards C0023015 Language handicap C0039590 Testicular neoplasms HSDN C3887638 Failure to thrive in infant C1855116 Methylmalonic aciduria, mut(-) type HPO C0009676 Confusion state C0236969 Substance-related disorders HSDN C3898969 Have been vomiting C0556520 Psychological desensitization HSDN C0151740 Intracranial hypertension C2316212 Cryopyrin-associated periodic syndromes MalaCards C0034150 Skin purpura C0008626 Congenital chromosomal disease HSDN C0020455 Hypergammaglobulinemia C0342731 Deficiency of mevalonate kinase HSDN C1557397 Adverse event associated with pain C0677866 Brain stem neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003860 Arteritis HSDN C3815497 Cough C0878675 Erdheim-chester disease MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0011884 Diabetic retinopathy HSDN C0013404 Respiratory difficulty C0349649 Pulmonary lymphangioleiomyomatosis MalaCards C0232847 Enuresis primary C0042024 Urinary incontinence UMLS C1279888 Proteinuria of undiagnosed cause C0041466 Typhoid fever HSDN C3887873 Hearing loss C0016542 Foreign body HSDN C0270948 Neurogenic muscular atrophy C2931183 Faces syndrome OrphaNet|MalaCards C0344315 Mood depressed C3280358 Wolfram-like syndrome, autosomal dominant OrphaNet|HPO|MalaCards C0020450 Hyperemesis gravidarum C0268450 Gitelman syndrome HSDN C2242996 Tingling C0036341 Schizophrenia HSDN C1549543 Administration method - pain C0162651 Gastric outlet obstruction HSDN C3887784 Decreased urine output C2909036 Twin twin transfusion HSDN C3641756 Have diarrhea C0023470 Myeloid leukemia HSDN C1963063 Anorexia adverse event C0027643 Neoplasm recurrence, local HSDN C0027066 Myoclonic jerking C1261473 Sarcoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0022423 Judgement HSDN C0476289 Gas pain C0810319 Other and unspecified gastrointestinal disorders UMLS C0032285 Pneum C0432222 Spondyloenchondrodysplasia MalaCards C0030552 Paralysis partial C0033586 Failure, prosthesis HSDN C0004134 Dyssynergia C1969053 Joubert syndrome 7 MalaCards|HPO C2911645 Weight loss adverse event C0035222 Respiratory distress syndrome, adult HSDN C0013362 Dysarthrias C0268468 Dystonia, dopa-responsive, due to sepiapterin reductase deficiency MalaCards|HPO C0151786 Weakness muscle C0039128 Syphilis HSDN C3539895 Pelvic pain occurs with bowel movement C0022116 Ischemia HSDN C3665347 Vision impaired C3551954 Coenzyme q10 deficiency, primary, 1 MalaCards C0004604 Pain back C0027663 Neoplasms, multiple primary HSDN C0700078 Deep tendon reflex decrease C4013360 Giant axonal neuropathy 2, autosomal dominant MalaCards C4084769 Vomiting frequency C1550639 Specimen type - fistula HSDN C4042891 Sleep wake disorders C1290398 Cerebral arterial aneurysm HSDN C3898969 Have been vomiting C0022650 Kidney calculi HSDN C0020455 Hypergammaglobulinemia C0001752 African swine fever HSDN C0019825 Voice hoarseness C2706915 Language:-:point in time:^patient:- HSDN C3274924 Have been coughing C0007570 Celiac disease HSDN C4084725 Usual severity cough C3495559 Juvenile arthritis HSDN C4085211 Pain distress question C0238417 Scorpion sting HSDN C2984058 Have pain C1963139 Hypopigmentation adverse event HSDN C1549543 Administration method - pain C1270972 Mild cognitive disorder HSDN C0009676 Confusion state C1522136 Hypernatremia result HSDN C4085317 Diarrhea frequency C0022423 Judgement HSDN C1963091 Diarrhea adverse event C1134719 Invasive ductal breast carcinoma HSDN C1549543 Administration method - pain C0034194 Pyloric stenosis HSDN C0042384 Vasculitis, nonspecific C2931785 Juvenile dermatomyositis OrphaNet|MalaCards C0478115 Oth spec symptom+signs involving circulat+respiratory sys C0178274 Arterial, arteriole and capillary diseases nos UMLS C0030554 Abnormal sensation C0026896 Myasthenia gravis MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0334419 Pheochromocytoma, malignant MalaCards C3827868 Tachycardia by ecg finding C2752015 Glycogen storage disease xiv MalaCards C0007859 Pain neck C0009404 Colorectal neoplasms HSDN C0700078 Deep tendon reflex decrease C0085920 Brachial neuralgia MalaCards C0460137 Push down or depress C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0020538 Hbp C0268381 Primary amyloidosis MalaCards C0018681 Headache, cephalalgia C3494419 Deformities, dentofacial HSDN C2919142 Short stature adverse event C1836315 Epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia MalaCards C0013604 Edematous C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C0041105 Jaw spasm C0043255 Stab wound HSDN C1963170 Hypothermia adverse event C0013595 Eczema HSDN C0011991 Loose stools C1306759 Eosinophilic disorder HSDN C2126090 Fainting while straining C0340854 Situational syncope UMLS C0026821 Cramp C0007873 Uterine cervical neoplasm HSDN C3898969 Have been vomiting C1879737 Aromatherapy and essential oils HSDN C4084784 Diarrhea C0398689 Hyper-igm immunodeficiency syndrome, type 1 HPO C1963091 Diarrhea adverse event C1832322 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive HPO C2237041 Shox gene with short stature C2931168 Hemangiomas, and cutaneous and intracranial vascular deformations MalaCards C0004134 Dyssynergia C0018018 Goat disease HSDN C4084775 Usual severity weight loss C0020875 Ileal diseases HSDN C1963184 Nystagmus adverse event C1860860 Neuhauser daly magnelli syndrome MalaCards C1971624 Appetite absent C0019693 Hiv infections HSDN C0036572 Convulsion C1845408 Contiguous abcd1-dxs1375e deletion syndrome MalaCards|HPO C0151889 Reflexes tendon increased C3281029 Rigidity and multifocal seizure syndrome, lethal neonatal MalaCards C1549543 Administration method - pain C0399526 Class iii malocclusion HSDN C3665492 Pigmentations C0027877 Neuronal ceroid-lipofuscinoses MalaCards C4085317 Diarrhea frequency C0021655 Insulin resistance HSDN C0009398 Color vision defects C0004364 Autoimmune diseases HSDN C0235153 Sensory hallucination C2936783 Colorectal cancer, hereditary nonpolyposis, type 1 MalaCards C0015300 Ocular proptosis C1837501 Microcephaly, primary autosomal recessive, 5 MalaCards C2017160 Left leg soft tissue swelling extending to the foot C0037580 Soft tissue swelling UMLS C4084725 Usual severity cough C2931916 Midline granulomatosis MalaCards C4084769 Vomiting frequency C0517555 Venous thrombosis after immobility HSDN C0184567 Pain acute C0023903 Liver neoplasms HSDN C2911645 Weight loss adverse event C1962971 Myocarditis adverse event HSDN C0518090 Frequency of pain question C0010035 Hereditary corneal dystrophy HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0205770 Choroid plexus papilloma HPO C0042963 Symptoms vomiting C0036202 Sarcoidosis HSDN C0035232 Diaphragmatic paralysis C0152025 Polyneuropathy HSDN C2024878 Cardiovascular surgery result: dyspnea C0014121 Bacterial endocarditis HSDN C0015672 Decreased energy C0950124 Papillomavirus infections HSDN C0026821 Cramp C0004933 Behavior modification technique HSDN C0042940 Disorder of voice C0152181 Hypoglossal nerve disease or syndrome HSDN C0040485 Wryneck C1546533 Specimen source codes - abscess HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0003493 Aortic diseases HSDN C1549543 Administration method - pain C0701818 Choledocholithiasis HSDN C0023015 Language handicap C1546847 Entity name part type - family HSDN C0027066 Myoclonic jerking C0017205 Gaucher disease HSDN C0042928 Paralysis vocal cord C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1334455 Pulmonary sclerosing hemangioma HSDN C0040264 Ear ringing sound C0038454 Cerebrovascular accident HSDN C0231218 Malaise generalized C0862953 Non-resectable cholangiocarcinoma UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0007222 Cardiovascular diseases HSDN C3887638 Failure to thrive in infant C2931001 Congenital disorder of glycosylation type 1g MalaCards C0042798 Vision dim C2930866 Ramos arroyo clark syndrome MalaCards C0242936 Center pain C0007124 Noninfiltrating intraductal carcinoma HSDN C0008031 Pain chest C0751674 Lymphangioleiomyomatosis OrphaNet|HSDN|HPO|MalaCards C0040460 Dental pain C0040445 Tooth mobility HSDN C4085210 Usual severity pain C0241910 Hepatitis, autoimmune HSDN C0026821 Cramp C0039984 Thoracic outlet syndrome MalaCards C0015230 Exanthem C1302794 Keratosis pilaris rubra UMLS C0015970 Fever unknown origin C2240374 Eosinophil count raised HSDN C0010200 Cough symptom C0030920 Peptic ulcer HSDN C1963091 Diarrhea adverse event C0011303 Demyelinating diseases HSDN C0040034 Thrombocytopenia C1857226 Dk phocomelia syndrome MalaCards C0037316 Not enough sleeping C0022758 Kap HSDN C0018524 Hallucinate C0030319 Panic disorder HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0242341 Sexual infantilism HSDN C4084775 Usual severity weight loss C0026936 Mycoplasma infections HSDN C3641756 Have diarrhea C0012814 Colon nos diverticulitis HSDN C0557874 Global developmental delay C1970203 Polyhydramnios, megalencephaly, and symptomatic epilepsy MalaCards|HPO C0497406 Over weight C0015302 External exotoses HSDN C0035229 Respiratory function impaired C0033822 Pseudomyxoma peritonei MalaCards C0027498 Nausea vomiting C0020473 Hyperlipidemia UMLS C0015672 Decreased energy C0011570 Mental depression UMLS C0004941 Behavioral symptoms C0023374 Lesch-nyhan syndrome OrphaNet|HPO|MalaCards C0019209 Large liver C1856401 Etfa deficiencies HPO C0015468 Face pain C0024950 Maxillary diseases HSDN C1069915 Vertigo C0152264 Familial erythrocytosis OrphaNet|HPO C3146279 Coma C0749098 Hematoma, subdural, acute HSDN C0015672 Decreased energy C3810814 Myocardial infarction ecg assessment HSDN C0162834 Hyperpigmentation C0017097 Gardner syndrome HPO C3641756 Have diarrhea C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0242936 Center pain C0016124 Finger injury HSDN C0027796 Neuralgias C0009088 Cluster headache UMLS C0349588 Stature short C0019569 Hirschsprung disease MalaCards|HPO C2984058 Have pain C0013312 Dupuytren contracture HSDN C0038002 Spleen enlargement C3887654 Polyarteritis nodosa, childhood-onset MalaCards C0424755 Fever symptoms C0003460 Anurias HSDN C0012833 Dizzy C0409959 Osteoarthritis, knee HSDN C0036572 Convulsion C1859359 Camptodactyly syndrome, guadalajara type i OrphaNet|UMLS|MalaCards C0017181 Gastrointestinal bleed C0268490 Tyrosinemia, type i MalaCards C3539893 Pelvic pain occurs with intercourse C0041582 Ulcer HSDN C1963090 Dehydration adverse event C0085548 Autosomal recessive polycystic kidney disease HPO C4085317 Diarrhea frequency C0149778 Soft tissue infections HSDN C1961131 Cough adverse event C0037274 Dermatologic disorders HSDN C0018784 Deafness sensorineural C0546952 Congenital facial asymmetry HSDN C0029163 Hemorrhage mouth C0018939 Hematological disease HSDN C0018772 Deafness C0085207 Gestational diabetes HSDN C0039070 Collapse fleeting C0025202 Melanoma HSDN C0917816 Deficiency mental C0175701 Aarskog syndrome MalaCards|HPO C0038990 Sweats C1859069 Brittle bone disorder OrphaNet C4084767 Bothered by vomiting C0017668 Focal glomerulosclerosis HSDN C2919142 Short stature adverse event C1836861 Fanconi anemia, complementation group i MalaCards|HPO C1384666 Decreased hearing C0524812 Intracranial hypotension HSDN C0024312 Lymphocytopenia C2936502 Charge syndrome, familial MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0039585 Androgen-insensitivity syndrome HSDN C0034155 Thrombotic thrombocytopenic purpura C3814778 Hemolytic index HSDN C0150055 Pain chronic C0015467 Neuralgia facial HSDN C3146279 Coma C0268579 Propionic acidemia HPO C0030232 Color loss C0305062 Tetanus toxoids HSDN C0518090 Frequency of pain question C0344435 Ventricular fibrillation by ecg finding HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0752347 Lewy body disease HSDN C1963180 Neck pain adverse event C0037274 Dermatologic disorders HSDN C4084768 Usual severity vomiting C1960459 Hereditary angioedema with normal c1 esterase inhibitor activity MalaCards C0004134 Dyssynergia C0334123 Histiocytosis, lipoid MalaCards C0038990 Sweats C3888018 Congenital hyperinsulinism MalaCards C0151786 Weakness muscle C4023182 Abnormality of muscle physiology UMLS C4084769 Vomiting frequency C0023487 Acute promyelocytic leukemia HSDN C4084784 Diarrhea C0013182 Drug allergy HSDN C1959630 Eye pain adverse event C0035305 Retinal detachment HSDN C0037317 Sleep disturbance C3150674 Chromosome 15q24 deletion syndrome HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0034530 Injury radiation HSDN C0027498 Nausea vomiting C3469605 Pseudohypoaldosteronism, type iid MalaCards C0860603 Anxiety symptom C0162565 Acute intermittent porphyria OrphaNet|HPO|MalaCards C0018772 Deafness C1306229 Dyschromatosis universalis OrphaNet|HPO|MalaCards C0011991 Loose stools C2911243 Encounter due to family history of colonic polyps HSDN C3641755 Have constipation C2981150 Uranostaphyloschisis HSDN C0026826 High muscle tone C0004361 Autogenic therapy HSDN C4084723 Constipation C0027819 Neuroblastoma HSDN C1963281 Vomiting adverse event C0004239 Atrial flutter HSDN C0010200 Cough symptom C0007138 Carcinoma, transitional cell HSDN C0851578 Disorder sleep C2239176 Liver carcinoma HSDN C0086439 Activity decreased C1868596 Atypical parkinson disease HPO C1279888 Proteinuria of undiagnosed cause C1567742 Alport syndrome, x-linked HPO C4084784 Diarrhea C0023440 Acute erythroblastic leukemia HSDN C0015672 Decreased energy C0014556 Epilepsy, temporal lobe HSDN C4084768 Usual severity vomiting C0205770 Choroid plexus papilloma HSDN|HPO C0013362 Dysarthrias C1135957 Narrative HSDN C4085211 Pain distress question C0206231 Bone malalignment HSDN C4084767 Bothered by vomiting C0033348 Language program HSDN C1963249 Tinnitus adverse event C2931205 Usher syndrome, type 1a MalaCards C0424755 Fever symptoms C0162651 Gastric outlet obstruction HSDN C3641756 Have diarrhea C0040247 Tinea HSDN C4085211 Pain distress question C0149654 Conduct disorder HSDN C4084788 Have dizziness C0016542 Foreign body HSDN C0349588 Stature short C2677682 Rett syndrome, zappella variant HPO C0030200 Intractable pain C0040034 Thrombocytopenia HSDN C4084768 Usual severity vomiting C0037313 Sleep HSDN C0011991 Loose stools C0042373 Vascular diseases HSDN C0016199 Pain flank C0015480 Disorder factitious HSDN C0242936 Center pain C1552527 Clinic / center - developmental disabilities HSDN C0576456 Poor feeding C2931246 Chromosome 17, trisomy 17p11 2 MalaCards C0151786 Weakness muscle C0023801 Lipomatosis HSDN C0086437 Joint hypermobility C1863732 Spondyloepimetaphyseal dysplasia with multiple dislocations MalaCards|HPO|UMLS C0007758 Cerebellar ataxia C0398746 Gluthathione synthetase deficiency MalaCards|HPO C1565249 Limitation, mobility C1861172 Venous thromboembolism HSDN C3815497 Cough C2931785 Juvenile dermatomyositis MalaCards C0150055 Pain chronic C1861329 Spinal canal stenosis HSDN C0015970 Fever unknown origin C0035592 Infection, rickettsiaceae HSDN C0426579 Anorexia symptom C0398367 Histiocytic necrotizing lymphadenitis OrphaNet|MalaCards C1963071 Back pain adverse event C0024299 Lymphoma HSDN C4085222 Nausea C0276357 Swine influenza MalaCards C2911647 Weight gain adverse event C0019080 Hemorrhage HSDN C0162298 Stiffness joints C1855606 Burton syndrome MalaCards C4084768 Usual severity vomiting C0282687 Hemorrhagic fever, ebola DiseaseOntology|MalaCards C3812171 Bradycardia by ecg finding C0268381 Primary amyloidosis MalaCards C0150055 Pain chronic C0021368 Inflammation HSDN C4084776 Weight loss C0003486 Aortic aneurysm HSDN C0030193 Sense of pain C0206620 Lymphangioma, cystic HSDN C0024031 Back pain lower back C1852522 Polydysspondyly HPO C4084802 Usual severity diarrhea C0017661 Iga glomerulonephritis HSDN C0026838 Spasticity muscle C0033975 Psychotic disorders HSDN C0010200 Cough symptom C0152902 Esophageal tuberculosis DiseaseOntology|MalaCards C0022638 Ketosis C4015186 Monocarboxylate transporter 1 deficiency MalaCards C4084767 Bothered by vomiting C0302148 Blood clot HSDN C0013604 Edematous C0022568 Keratitis HSDN C2911647 Weight gain adverse event C0039614 Tetanus HSDN C1553188 Hemolysis - observation C0019034 Hemoglobin sc disease MalaCards C1557397 Adverse event associated with pain C0027149 Myxoma HSDN C2984058 Have pain C0038325 Stevens-johnson syndrome HSDN C3463815 Feel fatigue C0850803 Anaphylaxis (non medication) HSDN C0016382 Cutaneous vascular engorgement C0867389 Chronic graft-versus-host disease MalaCards C0035078 Failure kidney C0431693 Renal cysts and diabetes syndrome OrphaNet|MalaCards C0030193 Sense of pain C0079173 Craniomandibular disorders HSDN C0497406 Over weight C0022865 Obstetric labor complications HSDN C3539893 Pelvic pain occurs with intercourse C0041952 Uerterolithiasis HSDN C3829611 Nausea frequency C1553188 Hemolysis - observation HSDN C0000737 Abdomen pain C0007273 Carotid artery diseases HSDN C0007398 Catatonic C0041296 Tuberculosis HSDN C0474368 Childbirth pain C0282333 Relaxation therapies HSDN C1959630 Eye pain adverse event C0349464 Wernicke-korsakoff syndrome HSDN C0015230 Exanthem C0857150 Neck rash UMLS C3641756 Have diarrhea C0025299 Meningocele HSDN C3539892 Pelvic pain in front C0037286 Skin neoplasms HSDN C4085549 Dizziness C0206255 Malaria vaccine HSDN C0041657 Consciousness loss C0001175 Acquired immunodeficiency syndrome HSDN C0002170 Alopecia disorders C1801959 Histiocytic medullary reticulosis (disorder) MalaCards|HPO C0018926 Emesis bloody C0038000 Spleen rupture HSDN C0030193 Sense of pain C0311277 Obesity, abdominal HSDN C4084769 Vomiting frequency C0241158 Cicatrix skin HSDN C3539891 Pelvic pain to the rear C0042253 Vaginal fistula HSDN C0020305 Fetal edema C0002878 Anemia, hemolytic HSDN C0011991 Loose stools C0032302 Mycoplasma pneumonia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0424318 Bullied HSDN C0042963 Symptoms vomiting C0041228 African trypanosomiasis HSDN C0032285 Pneum C0001768 Agammaglobulinemia OrphaNet|MalaCards C0000727 Abdomen acute C0015652 Fascioliasis HSDN C1510417 Apraxia of gait C0020701 Somatization disorder HSDN C0454644 Delayed language development C0795949 Galloway mowat syndrome HPO C1882272 Pain adverse event by ctcae anatomic descriptor C1532253 Sedentary lifestyle HSDN C0271215 Blindness legal C3541853 Nephronophthisis 15 MalaCards C0039070 Collapse fleeting C0039614 Tetanus HSDN C2911645 Weight loss adverse event C0001418 Adenocarcinoma HSDN C0727671 Red cross toothache drops C0026034 Microstomia HSDN C0085636 Light sensitivity C0265345 Lymphedema distichiasis syndrome OrphaNet|UMLS|HPO|MalaCards C1557397 Adverse event associated with pain C4085635 Appetite quality question HSDN C0349588 Stature short C4015067 Autoinflammation with infantile enterocolitis MalaCards C3539890 Pelvic pain causes awakening at night C0015732 Fecal incontinence HSDN C4084766 Vomiting C0032229 Pleural neoplasms HSDN C0557874 Global developmental delay C3502469 Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia OrphaNet|HPO|MalaCards C0009421 Comatose C0026850 Muscular dystrophy HSDN C0042025 Urinary incontinence stress C0034888 Rectal prolapse HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0008513 Chorioretinitis HSDN C2315100 Pediatric failure to thrive C1334229 Bowel dysplasia MalaCards C0042420 Vasovagal episode C4085311 Depression - recess HSDN C0018991 Paralysis one side of body C0032586 Polyradiculopathy HSDN C0497406 Over weight C1705812 Nci thesaurus role HSDN C2984058 Have pain C0178324 Blood vessel injury HSDN C0026603 Motion sickness C0037744 Perceptual spatial orientation HSDN C4085549 Dizziness C0282507 Heat stress disorders HSDN C0038002 Spleen enlargement C1866120 Autoimmune lymphoproliferative syndrome, type ib MalaCards|HPO C2984058 Have pain C0376527 Neoplasm, skull base HSDN C4085317 Diarrhea frequency C0027660 Neoplasms, glandular and epithelial HSDN C4085862 Bothered by nausea C1704972 Genomic orientation HSDN C0010200 Cough symptom C0004238 Atrial fibrillation HSDN C0751840 Pure alexia C0007774 Cerebral arterial diseases HSDN C3887638 Failure to thrive in infant C2930971 Acroosteolysis dominant type MalaCards|HPO C0424755 Fever symptoms C0032273 Pneumoconiosis HSDN C0020672 Body temperature decreased C0026269 Mitral valve stenosis HSDN C0020450 Hyperemesis gravidarum C0269663 Hyperemesis gravidarum, starting before the end of the 22nd week of gestation, with metabolic disturbance, such as dehydration UMLS C0018772 Deafness C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C0043094 Weight gain C0008350 Cholelithiasis HSDN C1963281 Vomiting adverse event C0039494 Temporomandibular joint disorders HSDN C0015469 Facial paralysis C0027830 Neurofibroma HSDN C0018681 Headache, cephalalgia C0037361 Olfactory sense HSDN C0030193 Sense of pain C0037305 Neoplasm, skull HSDN C0000731 Abdomen distention C0266283 Ectopic thyroid tissue (disorder) OrphaNet|HPO|MalaCards C0007398 Catatonic C0012746 Dissociative disorder HSDN C0037316 Not enough sleeping C0014548 Epilepsy, generalized HSDN C0011991 Loose stools C1304456 Congo hemorrhagic fever MalaCards C4082202 Sleep quality question C1261128 Progeria-like syndrome MalaCards C4084773 Bothered by weight gain C0344434 Atrial fibrillation ecg HSDN C1579931 Depressed - symptom C0795959 Gomez lopez hernandez syndrome MalaCards C0018772 Deafness C1578691 Congenital myxedema MalaCards C0026826 High muscle tone C3889476 Benign familial convulsion MalaCards C0460137 Push down or depress C0268281 Infantile neuronal ceroid lipofuscinosis MalaCards|HPO C0520909 Ponv C0001418 Adenocarcinoma HSDN C4084802 Usual severity diarrhea C1449842 Pseudohypoaldosteronism, type i, autosomal dominant HPO C0231471 Posture abnormality C1839564 Jensen syndrome MalaCards C1838869 Proximal neurogenic muscle weakness C2751805 Emery-dreifuss muscular dystrophy 5, autosomal dominant MalaCards|HPO C0750394 Wbc low C3151209 Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome HPO C2029884 Hearing loss by exam C0004933 Behavior modification technique HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0036341 Schizophrenia HSDN C0007758 Cerebellar ataxia C3280897 Joubert syndrome 15 MalaCards C0027497 Queasy C0032708 Disorders of porphyrin metabolism HSDN C0497247 Blood pressure elevation C1859568 Bardet-biedl syndrome 10 HPO C4084766 Vomiting C0031069 Familial mediterranean fever HSDN C0036572 Convulsion C1142430 Psychogenic seizure UMLS C0242936 Center pain C0038271 Stereotyped behavior HSDN C0851578 Disorder sleep C0236736 Cocaine-related disorders HSDN C0009421 Comatose C0008073 Developmental disabilities HSDN C1565249 Limitation, mobility C0460137 Push down or depress HSDN C4085548 Usual severity dizziness C0026782 Mumps vaccine HSDN C1963087 Constipation adverse event C0027145 Myxedema MalaCards C0010520 Skin cyanosis C0011581 Depressive disorder HSDN C1527344 Dysphonia C0206765 Connective and soft tissue neoplasm HSDN C0012833 Dizzy C0023676 Life style HSDN C1069915 Vertigo C0001973 Alcoholic intoxication, chronic HSDN C0034150 Skin purpura C0020676 Hypothyroidism HSDN C0522224 Palsied C0038019 Spondylosis HSDN C4084773 Bothered by weight gain C0034063 Pulmonary edema HSDN C0917816 Deficiency mental C0796264 Young-hughes syndrome OrphaNet|MalaCards C0221752 Rbc urine C1857761 Alagille syndrome 2 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C1704326 Role - roleclass HSDN C4085317 Diarrhea frequency C0019154 Hepatic vein thrombosis HSDN C1963063 Anorexia adverse event C1830398 Grooming:-:point in time:^patient:- HSDN C0917816 Deficiency mental C3551019 Choroideremia, deafness, and mental retardation MalaCards C0026838 Spasticity muscle C1552527 Clinic / center - developmental disabilities HSDN C0043094 Weight gain C0041466 Typhoid fever HSDN C0020578 Hyperventilate C1963090 Dehydration adverse event HSDN C3541349 Syncope C1762616 Meningioma, benign, no icd-o subtype MalaCards|HSDN C0033377 Caudal displacement C4048800 Telomeric 22q13 monosomy syndrome MalaCards C0013394 Coitus painful C0162809 Kallmann syndrome MalaCards|HPO C0013421 Dystonia C1963138 Hypertension adverse event HSDN C2315100 Pediatric failure to thrive C0018817 Atrial septal defects HSDN C4018871 Abnormality of the respiratory system C0043324 Juvenile xanthogranuloma MalaCards C0013911 Emaciate C0206643 Neoplasms, fibrous tissue HSDN C0008031 Pain chest C0009240 Cognition HSDN C4084775 Usual severity weight loss C0013336 Dwarfism HSDN C4085210 Usual severity pain C0041325 Peritonitis, tuberculous MalaCards|HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0014170 Endometrial neoplasms HSDN C3274924 Have been coughing C0001261 Actinomycosis HSDN C4084784 Diarrhea C0740340 Amyloidosis, familial HSDN C0015672 Decreased energy C0030977 Perceptual masking HSDN C0022346 Yellow skin C1546602 Specimen source codes - diverticulum HSDN C4084784 Diarrhea C0020542 Pulmonary hypertension HSDN C0231712 Gait waddling C1837657 Spondyloepiphyseal dysplasia, omani type MalaCards|UMLS C0022346 Yellow skin C0029882 Otitis media HSDN C0013404 Respiratory difficulty C3495801 Granulomatosis with polyangiitis HSDN C0151818 Opisthotonos C2749559 Methemoglobinemia, type i HPO C0151786 Weakness muscle C0003811 Cardiac arrhythmia HSDN C4084724 Usual severity constipation C0027765 Nervous system disorder HSDN C3898969 Have been vomiting C0024919 Behavior, maternal HSDN C0398650 Idiopathic thrombocytopenia purpura C2717961 Thrombotic microangiopathies HSDN C0018784 Deafness sensorineural C1845408 Contiguous abcd1-dxs1375e deletion syndrome MalaCards|HPO C0344434 Atrial fibrillation ecg C1843687 Atrial fibrillation, familial, 1 (disorder) MalaCards C1963093 Dizziness adverse event C0027658 Neoplasms, germ cell and embryonal HSDN C0003910 Articulation disorder C0040427 Tooth abnormalities HSDN C4084774 Have weight loss C0032227 Pleural effusion disorder HSDN C4084775 Usual severity weight loss C0022650 Kidney calculi HSDN C0010038 Corneal opacity disorder C1282359 Ocular cicatricial pemphigoid MalaCards C0232466 Feeding difficulty C1970431 Pitt-hopkins syndrome MalaCards C2242996 Tingling C1636667 Disorder characterized by eosinophilia HSDN C0036572 Convulsion C0264903 Premature ventricular complex multifocal MalaCards C0030486 Extremity paralysis, lower C0042164 Uveitis HSDN C0085593 Chill C0041321 Tuberculosis, miliary HSDN C0242936 Center pain C0031069 Familial mediterranean fever HSDN C4085211 Pain distress question C0004943 Behcet syndrome HSDN C0042798 Vision dim C0020538 Hypertensive disease HSDN C0007814 Cerebrospinal fluid otorrhea C0037198 Sinus thrombosis, intracranial HSDN C3641756 Have diarrhea C3149378 Immunodeficiency, common variable, 1 MalaCards|HPO C0474368 Childbirth pain C0152156 Dystocia HSDN C0013404 Respiratory difficulty C1710418 Thyroid gland teratoma UMLS C0042514 Ventricular tachycardia C3554047 Ventricular tachycardia, catecholaminergic polymorphic, 4 MalaCards C0700590 Diaphoresis excessive C0036161 Sandhoff disease HPO C3494358 Characteristic, prodromal C0039474 Temperament HSDN C0086565 Liver function abnormal C0854795 Resectable hepatic malignant neoplasm MalaCards C0038002 Spleen enlargement C0009447 Common variable immunodeficiency OrphaNet|HPO|MalaCards C0028738 Nystagmus C3280026 Hermansky-pudlak syndrome 9 MalaCards C0005745 Blepharoptosis C2930917 Chromosome 14, trisomy mosaic MalaCards C4084802 Usual severity diarrhea C0025500 Mesothelioma HSDN C4084784 Diarrhea C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C0013421 Dystonia C1846582 Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration HPO C0034150 Skin purpura C0037199 Sinusitis HSDN C0030193 Sense of pain C0021846 Intestinal polyps HSDN C0041657 Consciousness loss C0033941 Psychoses, substance-induced HSDN C0221166 Paraparesis C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0413252 Hypothermia due to exposure C0005686 Urinary bladder diseases HSDN C0020438 Hypercalciuria C0005974 Bone resorption HSDN C0271215 Blindness legal C1857618 Achromatopsia 2 HPO C0042571 Vertigo subjective C3244301 Coverage level - family HSDN C4042891 Sleep wake disorders C3539760 Mok wt allele HSDN C2911647 Weight gain adverse event C0024141 Lupus erythematosus, systemic HSDN C3163620 Hypotension adverse event C0268474 Hydroxykynureninuria MalaCards|HPO C0034155 Thrombotic thrombocytopenic purpura C0007781 Intracranial embolism and thrombosis HSDN C2242996 Tingling C0036677 Sensory threshold HSDN C0011168 Disorder deglutition C0796074 Mohr-tranebjaerg syndrome MalaCards|HPO C0036572 Convulsion C1000483 Genus anemia HSDN C0917816 Deficiency mental C1527231 Adrenomyeloneuropathy MalaCards C1549543 Administration method - pain C0040583 Tracheal stenosis HSDN C4084774 Have weight loss C0039483 Giant cell arteritis OrphaNet|HPO|MalaCards C0040485 Wryneck C1258223 Flavobacteriaceae infection HSDN C0000727 Abdomen acute C0013720 Ehlers-danlos syndrome HSDN C0332573 Macula C0456487 Peutz jeghers polyp MalaCards C0020458 Hyperhydrosis C3891556 Chromosome xq26.3 duplication syndrome MalaCards C0000737 Abdomen pain C2981625 Stage ii intrahepatic cholangiocarcinoma UMLS C0020438 Hypercalciuria C0265295 Jansen type metaphyseal chondrodysplasia HPO C3539892 Pelvic pain in front C1963088 Cystitis adverse event HSDN C0024902 Mastodynia C0003469 Anxiety disorders HSDN C0030200 Intractable pain C0812393 Cancer patients and suicide and depression HSDN C0085636 Light sensitivity C1412759 Bckdha gene HSDN C0013604 Edematous C0006663 Calcinosis HSDN C3898969 Have been vomiting C0027583 Nematode infections HSDN C0009421 Comatose C1704436 Peripheral arterial diseases HSDN C0009806 Constipate C0346407 Pancreatic polypeptide-oma MalaCards C1069915 Vertigo C0039538 Teratoma HSDN C0005745 Blepharoptosis C1527404 Female pseudo-turner syndrome HPO C0023380 Lethargy C1999266 Depression adverse event HSDN C4085549 Dizziness C0042075 Urologic diseases HSDN C0497247 Blood pressure elevation C0033300 Progeria OrphaNet|HPO C0011206 Delirium acute C0919267 Ovarian neoplasm HSDN C0041657 Consciousness loss C0752322 Epilepsy, partial, sensory HSDN C0239376 Lower extremity pain C0032807 Postphlebitic syndrome UMLS C0424755 Fever symptoms C1856143 Hemolytic uremic syndrome, typical MalaCards C3539892 Pelvic pain in front C1456865 Ureteral calculi HSDN C1963087 Constipation adverse event C0238027 Botulism, infantile OrphaNet|MalaCards C3714772 Fever recurrent C3887654 Polyarteritis nodosa, childhood-onset MalaCards|UMLS C1962972 Proteinuria adverse event C0035309 Retinal diseases HSDN C0007814 Cerebrospinal fluid otorrhea C0273483 Cranial nerve injury HSDN C3539895 Pelvic pain occurs with bowel movement C0012817 Diverticulum HSDN C0033774 Skin pruritus C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C0033774 Skin pruritus C0344434 Atrial fibrillation ecg HSDN C0005745 Blepharoptosis C0393591 Aicardi-goutieres syndrome MalaCards|HPO C0036572 Convulsion C1859092 Choroid plexus calcification and mental retardation OrphaNet|MalaCards C0003550 Broca aphasia C0033199 Proactive inhibition HSDN C0423707 Lateral femoral cutaneous neuralgia C0270891 Nerve plexus disorder, nos UMLS C0424755 Fever symptoms C1866495 Bartter syndrome, antenatal type 1 HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0029454 Osteopetrosis HSDN C4084784 Diarrhea C0022680 Polycystic kidney diseases HSDN C0004941 Behavioral symptoms C0342436 Diencephalic syndrome OrphaNet|MalaCards C4084724 Usual severity constipation C3537440 Cystinosis, infantile nephropathic OrphaNet|HPO|MalaCards C0000737 Abdomen pain C0007138 Carcinoma, transitional cell HSDN C0085636 Light sensitivity C0028738 Nystagmus HSDN C4084766 Vomiting C0013595 Eczema HSDN C2242996 Tingling C1997249 Neuralgia, pudendal MalaCards C3665492 Pigmentations C0546837 Malignant neoplasm of esophagus MalaCards C3887873 Hearing loss C0032453 Polychondritis, relapsing HSDN C2315100 Pediatric failure to thrive C0751267 Encephalopathy, subacute necrotizing, infantile MalaCards C4084766 Vomiting C1168250 Laryngopharyngeal reflux HSDN C4084802 Usual severity diarrhea C0273486 Cranial nerve x injury HSDN C1963071 Back pain adverse event C0016542 Foreign body HSDN C0018772 Deafness C3808971 Hypogonadotropic hypogonadism 17 with or without anosmia MalaCards C0030193 Sense of pain C0028879 Odontogenic cysts HSDN C0026826 High muscle tone C0410226 Congenital myotonic dystrophy MalaCards C0518090 Frequency of pain question C0027877 Neuronal ceroid-lipofuscinoses HSDN C0042571 Vertigo subjective C0038587 Substance withdrawal syndrome HSDN C0151786 Weakness muscle C0037773 Spastic paraplegia, hereditary HSDN C1963252 Tremor adverse event C0036946 Sheep--diseases HSDN C0037316 Not enough sleeping C0004275 Attitude health HSDN C0020455 Hypergammaglobulinemia C0032586 Polyradiculopathy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0391889 Bony union HSDN C0233993 Sexuality related problems C0234002 Sexual frustration UMLS C4084774 Have weight loss C2936797 Acid cholesteryl ester hydrolase deficiency, type 2 OrphaNet C3887873 Hearing loss C0024904 Mastoiditis HSDN C0037316 Not enough sleeping C3539923 Cdisc adas-cog - orientation summary score HSDN C0015402 Hemorrhage eye C0042345 Varicosity HSDN C0036572 Convulsion C3661744 Simple partial seizure with motor dysfunction, non-intractable UMLS C2024878 Cardiovascular surgery result: dyspnea C0032371 Poliomyelitis HSDN C0557874 Global developmental delay C0796232 Bohring syndrome OrphaNet|HPO|MalaCards C0034151 Hyperglobulinemic purpura C0027947 Neutropenia HSDN C1557397 Adverse event associated with pain C0022735 Klinefelter syndrome HSDN C0043094 Weight gain C0005779 Blood coagulation disorders HSDN C1963180 Neck pain adverse event C1458155 Mammary neoplasms HSDN C0003862 Pain joint C0042384 Vasculitis HSDN C2315100 Pediatric failure to thrive C0044707 11 beta hsd HPO C4085317 Diarrhea frequency C0024232 Lymphatic metastasis HSDN C3541349 Syncope C0018671 Head and neck neoplasms HSDN C0033790 Pseudobulbar palsy C0221056 Adult type dermatomyositis HSDN C0018932 Bright red rectal bleeding C0010346 Crohn disease MalaCards C0000737 Abdomen pain C3899981 Bclc stage a adult hepatocellular carcinoma UMLS C4084768 Usual severity vomiting C2937287 Hematolysis HSDN C0038002 Spleen enlargement C0268202 Beta-sitosterolemia MalaCards C1963065 Apnea adverse event C0032285 Pneumonia HSDN C0151686 Growth retardation C0152164 Cyclical vomiting syndrome (disorder) MalaCards C0426579 Anorexia symptom C0002351 Altitude sickness HSDN C0242936 Center pain C0032463 Polycythemia vera HSDN C0018681 Headache, cephalalgia C0029899 Otosclerosis HSDN C3641755 Have constipation C3151471 Amyloid cardiomyopathy, transthyretin-related HPO C0040264 Ear ringing sound C0037650 Somatoform disorder HSDN C0011991 Loose stools C0027660 Neoplasms, glandular and epithelial HSDN C1963281 Vomiting adverse event C0853697 Neutrophil count decreased HSDN C0036659 Sensation disorder C1963274 Vasculitis adverse event HSDN C0009421 Comatose C0036323 Schistosomiasis HSDN C0040822 D tremors C0085315 Toxoplasmosis, cerebral HSDN C0040485 Wryneck C0032851 Disease poultry HSDN C0027066 Myoclonic jerking C0037315 Sleep apnea syndromes HSDN C4084784 Diarrhea C0014805 Primary erythermalgia MalaCards|HPO C0151786 Weakness muscle C0751895 Vasospasm, intracranial HSDN C0850758 Pain pelvic C0282606 Myomatous neoplasm HSDN C0003862 Pain joint C0015397 Disorder of eye HSDN C1963252 Tremor adverse event C0022758 Kap HSDN C2187990 Unable to perform sex C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0020455 Hypergammaglobulinemia C2936664 Acquired hypogammaglobulinemia HSDN C0024312 Lymphocytopenia C3809383 Immunodeficiency 8 MalaCards C0013362 Dysarthrias C0524851 Neurodegenerative disorders HSDN C2911645 Weight loss adverse event C0004031 Aspergillosis, allergic bronchopulmonary OrphaNet|MalaCards C4085222 Nausea C1705811 Terminology role entity HSDN C3641756 Have diarrhea C0024788 Green monkey virus disease DiseaseOntology|OrphaNet|MalaCards C0042571 Vertigo subjective C0018916 Hemangioma HSDN C0751401 Ophthalmoparesis C0028866 Oculomotor nerve paralysis UMLS C1557397 Adverse event associated with pain C0520459 Necrotizing enterocolitis HSDN C3641755 Have constipation C0012817 Diverticulum HSDN C4042891 Sleep wake disorders C2706915 Language:-:point in time:^patient:- HSDN C0026821 Cramp C0027743 Nerve compression syndrome HSDN C1860844 Sparse, thin hair C1857276 Trichohepatoenteric syndrome MalaCards|HPO|UMLS C0002962 Angina C0221018 Hereditary sideroblastic anemia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0003047 Animal disease HSDN C1384666 Decreased hearing C0042373 Vascular diseases HSDN C0018772 Deafness C0029342 Orthomyxoviridae infections HSDN C0042571 Vertigo subjective C0024904 Mastoiditis HSDN C4085210 Usual severity pain C0020428 Hyperaldosteronism HSDN C2919142 Short stature adverse event C0206641 Osteochondromatosis OrphaNet|HPO C0020538 Hbp C1510455 Acrocephalosyndactylia OrphaNet|HPO|MalaCards C1557397 Adverse event associated with pain C0014571 Epiphyses, slipped HSDN C0011570 Monopolar depression C1836383 Spinocerebellar ataxia 27 HPO C0007758 Cerebellar ataxia C0018671 Head and neck neoplasms HSDN C0038002 Spleen enlargement C1835912 Aicardi-goutieres syndrome 4 MalaCards|HPO C0002962 Angina C0018552 Hamartoma HSDN C0221263 Cafe au lait spot C0030849 Penile neoplasms HSDN C0011991 Loose stools C1269683 Major depressive disorder HSDN C1549543 Administration method - pain C0028433 Nose neoplasms HSDN C0008031 Pain chest C0238357 Hyperkalemic periodic paralysis HPO C0427055 Face weakness C0282527 Infantile refsum disease (disorder) MalaCards|HPO C0020672 Body temperature decreased C0919267 Ovarian neoplasm HSDN C0035078 Failure kidney C0342289 Diabetes-deafness syndrome maternally transmitted (disorder) MalaCards|HPO C0232466 Feeding difficulty C0175693 Russell-silver syndrome MalaCards C0007398 Catatonic C0020538 Hypertensive disease HSDN C0036572 Convulsion C0030354 Papilloma HSDN C1963065 Apnea adverse event C2677109 Leukodystrophy, hypomyelinating, 4 MalaCards|HPO C0034150 Skin purpura C0038941 Incisional infection HSDN C4084769 Vomiting frequency C0019537 High pressure nervous syndrome HSDN C0039070 Collapse fleeting C0014863 Esophageal spasm diffuse HSDN C0020673 Hypothermia (central) (local) C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0242936 Center pain C0015409 Eye injuries penetrating HSDN C0037763 Spasm C0012691 Dislocations HSDN C4084766 Vomiting C0026946 Mycoses HSDN C2911647 Weight gain adverse event C0010246 Coxsackievirus infections HSDN C2919142 Short stature adverse event C1275081 Cardio-facio-cutaneous syndrome OrphaNet|HPO C2984058 Have pain C0678236 Rare diseases HSDN C4085222 Nausea C0004352 Autistic disorder HSDN C4084774 Have weight loss C0206171 Community acquired infections HSDN C0917816 Deficiency mental C0034341 Pyruvate carboxylase deficiency disease MalaCards|HPO C4085661 Usual severity nausea C1145670 Respiratory failure HSDN C4084784 Diarrhea C0011848 Diabetes insipidus HSDN C0040822 D tremors C0035801 Diseases rodent HSDN C1963091 Diarrhea adverse event C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C0009460 Communication impairment C0003646 Aptitude HSDN C0030193 Sense of pain C0013182 Drug allergy HSDN C0015672 Decreased energy C0700327 Clinical findings relating to memory HSDN C0234144 Dysgraphia C0175702 Williams syndrome OrphaNet|HPO|MalaCards C0332563 Papulae C0406817 Collagenoma, familial cutaneous OrphaNet|MalaCards C0009806 Constipate C0027662 Multiple endocrine neoplasia HSDN C0424755 Fever symptoms C1414542 Fbn1 gene HSDN C0013362 Dysarthrias C0268242 Niemann-pick disease, type a MalaCards C4084767 Bothered by vomiting C0004352 Autistic disorder HSDN C2919142 Short stature adverse event C3554446 Brachydactyly, type a1, c MalaCards C0009792 Consciousness disorder C0040136 Thyroid neoplasm HSDN C0234132 Pyramidal sign C1865864 Amyotrophic lateral sclerosis 5 MalaCards|UMLS C0973461 Dysphasia C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C0151311 Cranial nerve palsy C0025235 Melkersson-rosenthal syndrome OrphaNet|MalaCards C3887873 Hearing loss C0027627 Neoplasm metastasis HSDN C4085317 Diarrhea frequency C0035334 Retinitis pigmentosa HSDN C0150055 Pain chronic C1298685 Chronic pain syndrome UMLS C0042024 Urine incontinence C0025007 Measles HSDN C0242936 Center pain C0020557 Hypertriglyceridemia HSDN C4084773 Bothered by weight gain C3812171 Bradycardia by ecg finding HSDN C1069915 Vertigo C0030920 Peptic ulcer HSDN C0424755 Fever symptoms C0036095 Salivary gland neoplasms HSDN C0150055 Pain chronic C0042870 Vitamin d deficiency HSDN C4084724 Usual severity constipation C0041948 Uremia HSDN C0270948 Neurogenic muscular atrophy C3150801 Combined oxidative phosphorylation deficiency 7 MalaCards|HPO C0011168 Disorder deglutition C1842870 Chromosome 1p36 deletion syndrome OrphaNet|HPO|MalaCards C0015468 Face pain C0017638 Glioma HSDN C0023530 Leukopenia C1567741 Alport syndrome OrphaNet C4084766 Vomiting C3495559 Juvenile arthritis HSDN C0013428 Painful urination C0862601 Vaginal metastatic adenocarcinoma UMLS C1260880 Nasal drip C0275742 Whooping cough due to b. parapertussis MalaCards C4084775 Usual severity weight loss C0017638 Glioma HSDN C0020672 Body temperature decreased C1962979 Burn adverse event HSDN C0030200 Intractable pain C1548578 Location characteristic id - smoking HSDN C2984058 Have pain C0206762 Limb deformities, congenital HSDN C4085549 Dizziness C1963064 Anxiety adverse event HSDN C3898969 Have been vomiting C0162671 Melas syndrome HSDN C0038990 Sweats C0001206 Acromegaly OrphaNet|HPO|MalaCards C0013604 Edematous C1704272 Benign prostatic hyperplasia HSDN C4084769 Vomiting frequency C0025007 Measles HSDN C3539890 Pelvic pain causes awakening at night C0026857 Musculoskeletal diseases HSDN C0015469 Facial paralysis C0008441 Chondroblastoma HSDN C4084788 Have dizziness C0039538 Teratoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0001627 Congenital adrenal hyperplasia HSDN C0242936 Center pain C0242350 Erectile dysfunction HSDN C0085593 Chill C0035597 Pox rickettsial DiseaseOntology|MalaCards C0344315 Mood depressed C1858501 Spinocerebellar ataxia 12 MalaCards|HPO C4085661 Usual severity nausea C0334419 Pheochromocytoma, malignant MalaCards C2984057 Have nausea C0302148 Blood clot HSDN C2936821 Spinal cerebrospinal fluid leak C1290398 Cerebral arterial aneurysm HSDN C0151786 Weakness muscle C0010481 Cushing syndrome OrphaNet|MalaCards C0349588 Stature short C0795953 Masa syndrome (disorder) OrphaNet|HPO|MalaCards C3146279 Coma C0008628 Chromosome deletion HSDN C0042963 Symptoms vomiting C0017658 Glomerulonephritis HSDN C4084767 Bothered by vomiting C0008065 Childhood behavior HSDN C0013404 Respiratory difficulty C1843418 Niemann-pick disease, type f HPO C0030486 Extremity paralysis, lower C0018801 Heart failure HSDN C0018681 Headache, cephalalgia C0032326 Pneumothorax HSDN C0036572 Convulsion C0014121 Bacterial endocarditis HSDN C0030552 Paralysis partial C0206725 Subependymal glioma HSDN C0349588 Stature short C1148551 X-linked dyskeratosis congenita MalaCards|HPO C1557397 Adverse event associated with pain C0085395 Ureaplasma infections HSDN C0026884 Muteness C0751739 Basal ganglia cerebrovascular disease HSDN C0026838 Spasticity muscle C2984299 Asthma pathway HSDN C0150055 Pain chronic C0302826 Expressed emotion HSDN C0474368 Childbirth pain C0917715 Hajdu-cheney syndrome HSDN C0012833 Dizzy C0007774 Cerebral arterial diseases HSDN C0086437 Joint hypermobility C1853154 Nemaline myopathy 7 HPO C0042963 Symptoms vomiting C0079631 Interdisciplinary communication HSDN C2919142 Short stature adverse event C1860119 Acrofacial dysostosis syndrome of rodriguez MalaCards C0019825 Voice hoarseness C3553989 Spinal muscular atrophy, distal, autosomal recessive, 5 MalaCards C0030193 Sense of pain C0016658 Fracture bone HSDN C1549543 Administration method - pain C0039786 Therapeutic communities HSDN C0043144 Wheeze C0520538 Tracheobronchopathia osteoplastica MalaCards C0206160 Retic count elevated C0002895 Anemia, sickle cell OrphaNet|HPO|MalaCards C0751837 Gait ataxic C0014511 Epithelial cyst HSDN C4084768 Usual severity vomiting C0023434 Chronic lymphocytic leukemia HSDN C2911647 Weight gain adverse event C0024668 Mammary neoplasms, experimental HSDN C0742284 Chest pain atypical recurrent C0010054 Coronary arteriosclerosis UMLS C0031911 Pigment deposition C0278704 Malignant childhood neoplasm MalaCards C2911645 Weight loss adverse event C4041080 Neurocognitive disorders HSDN C2024878 Cardiovascular surgery result: dyspnea C0018567 Hand dermatoses HSDN C4085317 Diarrhea frequency C0009759 Conjunctival diseases HSDN C0424755 Fever symptoms C0206042 Fatal familial insomnia HPO C0042963 Symptoms vomiting C1864498 Renal tubular acidosis, distal, autosomal recessive MalaCards|HPO C4085317 Diarrhea frequency C0005940 Bone diseases HSDN C1961131 Cough adverse event C0033036 Atrial premature complexes HSDN C0812426 Kidney problem C0017665 Membranous glomerulonephritis UMLS C1549543 Administration method - pain C0014008 Empty sella syndrome HSDN C0015672 Decreased energy C0018790 Cardiac arrest HSDN C0030193 Sense of pain C0269116 Colon endometriosis UMLS C0036659 Sensation disorder C0085648 Synovial cyst HSDN C4084767 Bothered by vomiting C0403447 Chronic kidney insufficiency HSDN C1963071 Back pain adverse event C1258104 Diffuse scleroderma HSDN C0000731 Abdomen distention C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0026838 Spasticity muscle C2930820 Incontinentia pigmenti, familial male lethal type MalaCards|HPO C0030552 Paralysis partial C0236969 Substance-related disorders HSDN C0518090 Frequency of pain question C0010308 Congenital hypothyroidism HSDN C0020649 Blood pressure decreased C0221014 Reactive systemic amyloidosis OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0020619 Hypogonadism HSDN C4084775 Usual severity weight loss C0000833 Abscess HSDN C0008031 Pain chest C0034186 Pyelonephritis HSDN C0007758 Cerebellar ataxia C3665623 Serum albumin level decreased below normal HSDN C0030486 Extremity paralysis, lower C0017416 Genital neoplasms, female HSDN C3539892 Pelvic pain in front C0012746 Dissociative disorder HSDN C0013604 Edematous C0007133 Carcinoma, papillary HSDN C4085222 Nausea C0038362 Stomatitis HSDN C0020615 Hypoglycemia nos C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|HPO|MalaCards C2032395 Pelvic pain on the left C0600041 Infective cystitis HSDN C0018772 Deafness C0015456 Facial dermatoses HSDN C0017181 Gastrointestinal bleed C0031269 Peutz-jeghers syndrome OrphaNet|HPO|MalaCards C0023012 Delay language C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO C4084802 Usual severity diarrhea C0239981 Hypoalbuminemia HSDN C0349588 Stature short C3151120 Meier-gorlin syndrome 4 MalaCards C4084769 Vomiting frequency C0008149 Chlamydia infections HSDN C4084773 Bothered by weight gain C1522133 High cholesterol level HSDN C0151311 Cranial nerve palsy C2985524 Rhabdoid tumor predisposition syndrome MalaCards C0152459 Striae C0033847 Pseudoxanthoma elasticum OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0027831 Neurofibromatosis 1 HSDN C0012833 Dizzy C0005974 Bone resorption HSDN C2911647 Weight gain adverse event C0031149 Peritoneal neoplasms HSDN C0042024 Urine incontinence C0011849 Diabetes mellitus HSDN C4085210 Usual severity pain C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C0012833 Dizzy C0026848 Myopathy HSDN C4084723 Constipation C2936346 22q11 deletion syndrome OrphaNet|HPO|MalaCards C0019209 Large liver C3665770 Acquired lipoatrophic diabetes MalaCards C0426579 Anorexia symptom C0007222 Cardiovascular diseases HSDN C0040034 Thrombocytopenia C1861178 Thrombocytopenia paris-trousseau type MalaCards C0043094 Weight gain C0001624 Adrenal gland neoplasms HSDN C0002962 Angina C0032226 Pleural diseases HSDN C0030193 Sense of pain C0010073 Coronary artery vasospasm HSDN C2911647 Weight gain adverse event C0022408 Arthropathy HSDN C2984058 Have pain C0026771 Trauma multiple HSDN C0751295 Memory loss or impairment C0023795 Lipoid proteinosis of urbach and wiethe HPO C1549543 Administration method - pain C0041974 Urethral stricture HSDN C0011206 Delirium acute C0006112 Brain diseases, metabolic HSDN C0030193 Sense of pain C0013505 Cyst, pulmonary hydatid HSDN C0013421 Dystonia C2984299 Asthma pathway HSDN C4085862 Bothered by nausea C0037397 Behavior social HSDN C0013604 Edematous C0027660 Neoplasms, glandular and epithelial HSDN C0022346 Yellow skin C0034065 Pulmonary embolism HSDN C0005745 Blepharoptosis C0015938 Fetal macrosomia MalaCards C0023012 Delay language C1835088 Maxillofacial dysostosis MalaCards C1963180 Neck pain adverse event C0458219 Complex regional pain syndromes HSDN C0018777 Deafness, conductive C0027651 Tumor HSDN C4085317 Diarrhea frequency C0020413 Hymenolepiasis DiseaseOntology|HSDN C4084775 Usual severity weight loss C0032962 Pregnancy complications HSDN C4084767 Bothered by vomiting C0032226 Pleural diseases HSDN C0031911 Pigment deposition C1334691 Melanomatosis MalaCards C0009421 Comatose C0040558 Toxoplasmosis HSDN C0036659 Sensation disorder C1556061 Electric injuries HSDN C0038999 Swelling C0396023 Chronic adenoiditis DiseaseOntology|MalaCards C4084723 Constipation C0206042 Fatal familial insomnia HPO C4084767 Bothered by vomiting C0152998 Acute nonparalytic poliomyelitis, poliovirus, unspecified type DiseaseOntology|MalaCards C1963281 Vomiting adverse event C0012644 Animal disease models HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0302182 Trabecular adenocarcinoma MalaCards C1963249 Tinnitus adverse event C1858916 Deafness, autosomal dominant 16 MalaCards C0020458 Hyperhydrosis C1854336 Paragangliomas 3 MalaCards|HPO C1961131 Cough adverse event C1322286 Thymoma, type c OrphaNet|MalaCards C0013604 Edematous C2945560 Hemolytic HSDN C0034150 Skin purpura C0085110 Severe combined immunodeficiency HSDN C4085317 Diarrhea frequency C2984302 Leishmaniasis infection pathway HSDN C0036572 Convulsion C3661551 Complex partial epileptic seizure of temporal lobe UMLS C0030486 Extremity paralysis, lower C1956346 Coronary artery disease HSDN C0557874 Global developmental delay C3151857 Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism MalaCards C0000737 Abdomen pain C0023473 Myeloid leukemia, chronic HSDN C0011168 Disorder deglutition C3280226 Spinocerebellar ataxia, autosomal recessive 11 MalaCards C4084773 Bothered by weight gain C0002989 Epithelioid hemangioma of skin HSDN C0151908 Dry skin C0271695 Rabson-mendenhall syndrome OrphaNet|HPO|UMLS C0020455 Hypergammaglobulinemia C0009326 Collagen diseases HSDN C0013604 Edematous C0035410 Rhabdomyolysis HSDN C1963071 Back pain adverse event C0005942 Bone diseases, endocrine HSDN C1971624 Appetite absent C0023904 Liver neoplasms, experimental HSDN C0027796 Neuralgias C0152054 Therapeutic touch HSDN C1549543 Administration method - pain C0010035 Hereditary corneal dystrophy HSDN C1963071 Back pain adverse event C0018571 Hand injury HSDN C0018772 Deafness C0007137 Squamous cell carcinoma HSDN C0036572 Convulsion C2718304 Sulfoiduronate sulfatase deficiency OrphaNet C3539895 Pelvic pain occurs with bowel movement C0037274 Dermatologic disorders HSDN C0036572 Convulsion C0032019 Pituitary neoplasms HSDN C0270846 Astatic seizure C2677326 Epileptic encephalopathy, early infantile, 4 MalaCards C0014724 Burping C0011168 Deglutition disorders HSDN C0042963 Symptoms vomiting C0524910 Hepatitis c, chronic MalaCards C2237041 Shox gene with short stature C2678039 Mental retardation, x-linked, syndromic 9 MalaCards C0027066 Myoclonic jerking C1546847 Entity name part type - family HSDN C4084776 Weight loss C0149514 Bronchitis acute HSDN C0042798 Vision dim C4015371 Macular dystrophy with central cone involvement MalaCards C2984058 Have pain C0042065 Genitourinary neoplasms HSDN C4084723 Constipation C0023530 Leukopenia HSDN C0018524 Hallucinate C0702221 Tactual discrimination HSDN C0042963 Symptoms vomiting C0035457 Rhinitis, allergic, perennial HSDN C0018772 Deafness C0702166 Acne HSDN C0231218 Malaise generalized C0024307 Lymphomatoid granulomatosis UMLS C0085593 Chill C0152938 Secondary pneumonic plague DiseaseOntology|MalaCards C0751837 Gait ataxic C0042594 Vestibular diseases HSDN C1549543 Administration method - pain C0011405 Pulp disorder HSDN C0004134 Dyssynergia C0036974 Shock HSDN C0040485 Wryneck C1290143 Disorders musculoskeletal neck UMLS C2315100 Pediatric failure to thrive C1970456 Surfactant metabolism dysfunction, pulmonary, 3 MalaCards|HPO C0020538 Hbp C0002986 Fabry disease MalaCards|HPO C1557397 Adverse event associated with pain C0022374 Jejunal neoplasms HSDN C0085636 Light sensitivity C2675066 Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus HPO C0424755 Fever symptoms C0040592 Trachoma HSDN C0038506 Stutter C3146297 Study of behavior during childhood HSDN C2096293 Ent surgical result ear vertigo C0032453 Polychondritis, relapsing OrphaNet|MalaCards C1963252 Tremor adverse event C1510460 Orofaciodigital syndrome i MalaCards|HPO C0026838 Spasticity muscle C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards|UMLS C0003078 Aniseikonia C0809996 Blindness and vision defects UMLS C0041667 Low weight C4015461 Ruijs-aalfs syndrome MalaCards C0018524 Hallucinate C0017638 Glioma HSDN C1384666 Decreased hearing C1412749 Bbs4 gene HPO C1963281 Vomiting adverse event C1963266 Uveitis adverse event HSDN C0018784 Deafness sensorineural C0007138 Carcinoma, transitional cell HSDN C1963065 Apnea adverse event C0026961 Mydriasis HSDN C0019079 Bloody sputum C2931854 Allergic bronchopulmonary mycosis MalaCards C3146279 Coma C0041466 Typhoid fever MalaCards C0151786 Weakness muscle C0002792 Anaphylaxis HSDN C0042963 Symptoms vomiting C0037036 Sialorrhea HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C1455705 Pulmonary histiocytosis x MalaCards C1549543 Administration method - pain C0085392 Bacteroidaceae infection HSDN C0574988 Elbow joint laxity C2676510 Spondylocheirodysplasia, ehlers-danlos syndrome-like UMLS C4085210 Usual severity pain C0042258 Vaginal neoplasms HSDN C3541349 Syncope C0001122 Acidosis HSDN C0473383 Edema or excessive weight gain in pregnancy - not delivered C0028754 Obesity UMLS C0009398 Color vision defects C0154778 Myopia, degenerative HSDN C4084774 Have weight loss C0024809 Marijuana abuse HSDN C0022107 Fussiness C0751120 Benign infantile myoclonic epilepsy OrphaNet|MalaCards C3641756 Have diarrhea C0004352 Autistic disorder HSDN C3641755 Have constipation C0017689 Glucagonoma OrphaNet|MalaCards C2919142 Short stature adverse event C0265965 Dyskeratosis congenita OrphaNet|HPO|MalaCards C4042891 Sleep wake disorders C0006663 Calcinosis HSDN C4085211 Pain distress question C1306759 Eosinophilic disorder HSDN C1962972 Proteinuria adverse event C1456781 Benign melanocytic nevus HSDN C0151889 Reflexes tendon increased C1846046 Spastic paraplegia 16, x-linked (disorder) MalaCards C4084726 Distress cough C0025202 Melanoma HSDN C2237041 Shox gene with short stature C1848413 Trichothiodystrophy, type 1 MalaCards C4085210 Usual severity pain C3889576 Euphoria HSDN C0037771 Paraparesis spastic C0027765 Nervous system disorder HSDN C4084802 Usual severity diarrhea C0020456 Hyperglycemia HSDN C0036659 Sensation disorder C0003850 Arteriosclerosis HSDN C0013404 Respiratory difficulty C0029463 Osteosarcoma HSDN C0020673 Hypothermia (central) (local) C0027902 Neuropsychological diagnosis HSDN C3887638 Failure to thrive in infant C0016065 Polyostotic fibrous dysplasia HSDN C1963071 Back pain adverse event C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0036396 Sciatica C0021400 Influenza HSDN C4084726 Distress cough C2981150 Uranostaphyloschisis HSDN C4084774 Have weight loss C0023890 Liver cirrhosis HSDN C0004134 Dyssynergia C0038160 Staphylococcal infections HSDN C0424755 Fever symptoms C1963229 Retinal detachment adverse event HSDN C0036572 Convulsion C3697594 Post-cerebrovascular accident epilepsy UMLS C4085661 Usual severity nausea C0085207 Gestational diabetes HSDN C0004604 Pain back C1963084 Colitis adverse event HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0553980 Endomyocardial fibrosis HSDN C1549543 Administration method - pain C0014347 Enterobacteriaceae infections HSDN C1384666 Decreased hearing C3554168 Combined oxidative phosphorylation deficiency 14 MalaCards C3665347 Vision impaired C1842914 Adult-onset vitelliform macular dystrophy OrphaNet|HPO|MalaCards C0038990 Sweats C1849321 Sandhoff disease, juvenile type HPO C0040264 Ear ringing sound C1556682 Adverse event associated with infection HSDN C0340288 Angina stable C0003843 Arterio arterial fistula HSDN C0013421 Dystonia C0085388 Intracranial tuberculoma HSDN C4084766 Vomiting C0024117 Chronic obstructive airway disease HSDN C2984057 Have nausea C0027831 Neurofibromatosis 1 HSDN C1962972 Proteinuria adverse event C0239981 Hypoalbuminemia HSDN C0018784 Deafness sensorineural C1090821 Sepsis (invertebrate) HSDN C0022107 Fussiness C1412573 Asah1 gene HPO C2242996 Tingling C0020941 Immersion foot HSDN C2237041 Shox gene with short stature C2931720 Fronto-facio-nasal dysostosis OrphaNet|MalaCards C3641755 Have constipation C0020621 Hypokalemia HSDN C0027066 Myoclonic jerking C0393571 Multiple system atrophy HSDN C1557397 Adverse event associated with pain C0024809 Marijuana abuse HSDN C2364082 Hyposmia C1855739 Indifference to pain, congenital, autosomal recessive HPO|UMLS C0086565 Liver function abnormal C3280240 Microcephaly, epilepsy, and diabetes syndrome MalaCards C0221232 Welts C0042111 Urticaria pigmentosa UMLS C4084767 Bothered by vomiting C0024788 Green monkey virus disease DiseaseOntology|MalaCards C0034150 Skin purpura C0009677 Congenital macroglossia HSDN C0042755 Virilisation C0020595 Hypoaldosteronism HSDN C3463815 Feel fatigue C0004364 Autoimmune diseases HSDN C0043094 Weight gain C0019569 Hirschsprung disease HSDN C1263846 Attention deficit disorder with hyperactivity C2674949 Chromosome 3q29 deletion syndrome MalaCards C0036572 Convulsion C0003469 Anxiety disorders HSDN C0398650 Idiopathic thrombocytopenia purpura C0023480 Leukemia, myelomonocytic, chronic HSDN C4084802 Usual severity diarrhea C0007120 Bronchioloalveolar adenocarcinoma HSDN C3829611 Nausea frequency C0220654 Meningeal carcinomatosis HSDN C4084725 Usual severity cough C0034362 Q fever DiseaseOntology|MalaCards C0036572 Convulsion C1861967 Basal ganglia calcification, idiopathic, childhood-onset UMLS C1549543 Administration method - pain C0151491 Congenital musculoskeletal anomalies HSDN C0151786 Weakness muscle C0019364 Herpes zoster ophthalmicus HSDN C0013604 Edematous C0241910 Hepatitis, autoimmune HSDN C2203646 Jaundice C1458156 Recurrent malignant neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0013386 Dyskinesia, drug-induced HSDN C1963135 Hepatic necrosis adverse event C0349535 Carcinoid tumor of intestine MalaCards C0002962 Angina C0031350 Pharyngitis HSDN C0037199 Sinus infection C2931916 Midline granulomatosis MalaCards C0497406 Over weight C0000786 Spontaneous abortion HSDN C0013404 Respiratory difficulty C1710175 Squamous cell lung carcinoma, papillary variant UMLS C0027066 Myoclonic jerking C0029944 Drug overdose HSDN C3887873 Hearing loss C1423541 Vangl2 gene HSDN C0427055 Face weakness C1837094 Myasthenic syndrome, congenital, ie MalaCards|HPO C0973461 Dysphasia C0265241 Franceschetti-klein syndrome MalaCards|HPO C3274924 Have been coughing C1963138 Hypertension adverse event HSDN C1963184 Nystagmus adverse event C1848932 Tapetoretinal degeneration with ataxia MalaCards C3898969 Have been vomiting C0239189 Disaccharide intolerance MalaCards C0242936 Center pain C0018922 Hemangiopericytoma HSDN C0030193 Sense of pain C0021890 Intraoperative complications HSDN C0030554 Abnormal sensation C0024693 Mandible injury HSDN C0917816 Deficiency mental C2931484 Cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation OrphaNet|MalaCards C0009421 Comatose C0008775 Ciguatera poisoning HSDN C0150055 Pain chronic C0015745 Ingestive behavior HSDN C0024031 Back pain lower back C0221204 Lytic lesion HSDN C4084773 Bothered by weight gain C0001349 Acute-phase reaction HSDN C0028961 Urine output decreased C0460137 Push down or depress HSDN C0033377 Caudal displacement C3266101 22q11 partial monosomy syndrome OrphaNet|HPO C0427055 Face weakness C1836122 Sarcoidosis, early-onset MalaCards C0030193 Sense of pain C0242659 Female homosexual HSDN C0009398 Color vision defects C2984299 Asthma pathway HSDN C0241165 Skin thickening C0268494 Oculocutaneous albinism type 1 MalaCards C0349588 Stature short C1421143 Trh gene HPO C1384666 Decreased hearing C0009324 Ulcerative colitis HSDN C0917816 Deficiency mental C3502492 Microcephaly with chorioretinopathy, autosomal recessive OrphaNet|HPO|MalaCards C2364111 Gustatory anesthesia C0027873 Neuromyelitis optica HSDN C3146279 Coma C0003850 Arteriosclerosis HSDN C0037763 Spasm C0037286 Skin neoplasms HSDN C0039070 Collapse fleeting C0019195 Hepatitis, viral, human HSDN C2029884 Hearing loss by exam C4048196 Beta-mannosidosis HSDN C3887873 Hearing loss C0015663 Fasting HSDN C1963093 Dizziness adverse event C0031118 Peripheral nervous system neoplasms HSDN C0030193 Sense of pain C1336264 Paranasal sinus cancer stage iii UMLS C3274924 Have been coughing C1258104 Diffuse scleroderma HSDN C0427190 Ataxia, truncal C1846367 Spinocerebellar ataxia 19 HPO|UMLS C0009676 Confusion state C0020524 Disorders of excessive somnolence HSDN C0030193 Sense of pain C0035335 Retinoblastoma HSDN C1384666 Decreased hearing C0917715 Hajdu-cheney syndrome OrphaNet|HPO C0004604 Pain back C0032226 Pleural diseases HSDN C4085210 Usual severity pain C0423772 Cutaneous fistula HSDN C0019209 Large liver C3280054 Geleophysic dysplasia 2 MalaCards C4084784 Diarrhea C0009442 Common bile duct neoplasms HSDN C0151908 Dry skin C0024137 Lupus erythematosus, cutaneous OrphaNet C1963071 Back pain adverse event C0010356 Cross infection HSDN C1961131 Cough adverse event C0021818 Intervertebral disk displacement HSDN C4085210 Usual severity pain C0024312 Lymphopenia HSDN C3539891 Pelvic pain to the rear C0520676 Premenstrual dysphoric disorder HSDN C0028738 Nystagmus C2931891 Necrotizing encephalopathy, infantile subacute, of leigh MalaCards|HPO C1963091 Diarrhea adverse event C0543514 Glycogen storage disease ixb HPO C1579931 Depressed - symptom C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant HPO C0013404 Respiratory difficulty C0004245 Atrioventricular block HSDN|UMLS C0020580 Decreased sensation C0038017 Congenital spondylolisthesis HSDN C3641756 Have diarrhea C0029410 Osteoarthritis of hip HSDN C3539895 Pelvic pain occurs with bowel movement C0085096 Peripheral vascular diseases HSDN C3463815 Feel fatigue C0040820 Trematode infections HSDN C0401149 Constipation chronic C0281479 Primary systemic amyloidosis MalaCards C0013604 Edematous C0019061 Hemolytic-uremic syndrome HSDN C0018681 Headache, cephalalgia C1708998 Metastatic adrenal gland chromaffin neoplasm UMLS C0454644 Delayed language development C2675369 Chromosome 22q11.2 microduplication syndrome OrphaNet|HPO C2700617 Irritation - emotion C2749659 Aicardi-goutieres syndrome 5 (disorder) MalaCards C4084724 Usual severity constipation C0015802 Femur fracture HSDN C0009080 Finger clubbing C0029411 Osteoarthropathy, primary hypertrophic HPO C3463815 Feel fatigue C0019326 Ventral hernia HSDN C0042798 Vision dim C3553951 Peroxisome biogenesis disorder 7b MalaCards C0012833 Dizzy C0155519 Labyrinth reactiv.loss-unilat. UMLS C1963093 Dizziness adverse event C0428953 Ecg infarction myocardial HSDN C3539891 Pelvic pain to the rear C0022410 Joint instability HSDN C4084775 Usual severity weight loss C0019284 Diaphragmatic hernia HSDN C0003910 Articulation disorder C0393593 Dystonia disorders HSDN C3898969 Have been vomiting C0948089 Acute coronary syndrome HSDN C0036572 Convulsion C2169807 Recurrent nonepileptic seizures UMLS C0030552 Paralysis partial C0270726 Alexander disease MalaCards C0037384 Snore C0029896 Disease, ent HSDN C1962972 Proteinuria adverse event C0016169 Pathologic fistula HSDN C3641755 Have constipation C0022876 Premature obstetric labor HSDN C4084776 Weight loss C0010418 Cryptosporidiosis DiseaseOntology|HSDN C0018965 Blood urine C1866552 Paragangliomas 2 (disorder) MalaCards C0036572 Convulsion C0043253 Trauma blunt HSDN C1549543 Administration method - pain C0015302 External exotoses HSDN C4084788 Have dizziness C0007786 Brain ischemia HSDN C4084773 Bothered by weight gain C0033839 Pseudorabies HSDN C0042755 Virilisation C0029405 Osteitis fibrosa cystica HSDN C0036572 Convulsion C0041330 Tuberculosis, spinal HSDN C0020455 Hypergammaglobulinemia C1963234 Serum sickness adverse event HSDN C0043094 Weight gain C0034885 Rectal neoplasms HSDN C1963077 Bone pain adverse event C0700095 Central neuroblastoma MalaCards C0018524 Hallucinate C0023343 Leprosy HSDN C0242936 Center pain C0010481 Cushing syndrome HSDN C0020538 Hbp C2931667 Fitzsimmons walson mellor syndrome MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0001430 Adenoma HSDN C0007384 Cataplexy C1834372 Narcolepsy 1 MalaCards|HPO C3887638 Failure to thrive in infant C0265251 Oto-palato-digital syndrome type 1 MalaCards C0004134 Dyssynergia C0034960 Refsum disease OrphaNet|HPO C1963281 Vomiting adverse event C1636667 Disorder characterized by eosinophilia HSDN C1963087 Constipation adverse event C0037019 Shy-drager syndrome HSDN C0234132 Pyramidal sign C0751383 Juvenile neuronal ceroid lipofuscinosis OrphaNet|MalaCards C0009806 Constipate C0029458 Osteoporosis, postmenopausal HSDN C0040485 Wryneck C0028866 Oculomotor nerve paralysis HSDN C3898969 Have been vomiting C0268600 3-methylcrotonyl coa carboxylase 1 deficiency MalaCards|HPO C0011991 Loose stools C0022104 Irritable bowel syndrome UMLS C0023530 Leukopenia C0585216 Alpha-thalassemia myelodysplasia syndrome OrphaNet|HPO C0032227 Effusion pleural C0149951 Ovarian fibromata OrphaNet|MalaCards C4085211 Pain distress question C0013449 Ear neoplasms HSDN C0013604 Edematous C0007965 Chediak-higashi syndrome OrphaNet|HPO|MalaCards C0478664 Lymphadenopathy regional C0543786 Debre's syndrome MalaCards C0007166 Cardiac output decreased C0002949 Aneurysm, dissecting HSDN C2919142 Short stature adverse event C0344487 Lateral meningocele MalaCards C4084769 Vomiting frequency C0003869 Arthritis, infectious HSDN C2024893 Cardiovascular surgery result: fatigue C0206702 Klatskin tumor MalaCards C4084802 Usual severity diarrhea C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C0007758 Cerebellar ataxia C0043325 Xanthomatosis HSDN C4085211 Pain distress question C0032578 Polyploidy HSDN C0151825 Ostalgia C0700095 Central neuroblastoma MalaCards C0086437 Joint hypermobility C0796094 Blepharophimosis syndrome ohdo type MalaCards|UMLS C0012833 Dizzy C0015745 Ingestive behavior HSDN C0005745 Blepharoptosis C3151302 Chromosome 13q14 deletion syndrome MalaCards C0018772 Deafness C1785148 Rapp-hodgkin syndrome HPO C1856661 Cornea cloudy C1854896 Mucolipidosis iii gamma MalaCards|HPO C3665492 Pigmentations C1335398 Gastric peutz-jeghers polyp MalaCards C4084774 Have weight loss C0043168 Whooping cough due to unspecified organism HSDN C0030193 Sense of pain C0018994 Hemobilia HSDN C1962972 Proteinuria adverse event C0039590 Testicular neoplasms HSDN C0033774 Skin pruritus C0022595 Keratosis follicularis OrphaNet|HPO C0242936 Center pain C0029440 Osteoma HSDN C0005745 Blepharoptosis C0079661 Klein's syndrome MalaCards C0241137 Skin pallor C0334419 Pheochromocytoma, malignant MalaCards C4085317 Diarrhea frequency C0024668 Mammary neoplasms, experimental HSDN C4084776 Weight loss C0041374 Tumor virus infections HSDN C0231528 Muscle pain generalized C0268344 Ehlers-danlos syndrome 6b OrphaNet|HPO|MalaCards C4084767 Bothered by vomiting C0027743 Nerve compression syndrome HSDN C0349588 Stature short C1969607 Kallmann syndrome 2 with selective tooth agenesis HPO C0497406 Over weight C0020676 Hypothyroidism HSDN C1963093 Dizziness adverse event C3809645 Basal ganglia calcification, idiopathic, 5 MalaCards C4084766 Vomiting C0032987 Ectopic pregnancy HSDN C1836296 Lower extremity weakness C2676732 Spastic paraplegia 38, autosomal dominant (disorder) MalaCards|UMLS C0042024 Urine incontinence C0032371 Poliomyelitis HSDN C0018681 Headache, cephalalgia C0009319 Colitis HSDN C4042891 Sleep wake disorders C0004623 Bacterial infections HSDN C1000483 Genus anemia C1850127 Osteopetrosis, autosomal recessive 1 MalaCards|HPO C4084774 Have weight loss C0015934 Fetal growth retardation HSDN C0004134 Dyssynergia C1849321 Sandhoff disease, juvenile type HPO C2984057 Have nausea C0024198 Lyme disease HSDN C0019825 Voice hoarseness C0278726 Small cell lung cancer extensive stage UMLS C4084802 Usual severity diarrhea C0037354 Smallpox HSDN C0034933 Abnormal reflexes C3495422 Finding relating to sexuality and sexual activity HSDN C0242936 Center pain C0021099 Impetigo HSDN C0022346 Yellow skin C0004935 Animal ethology HSDN C0557874 Global developmental delay C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C0236969 Substance-related disorders HSDN C0518090 Frequency of pain question C0011875 Diabetic angiopathies HSDN C4084784 Diarrhea C0342873 Glutaric aciduria iii MalaCards|HPO C0035232 Diaphragmatic paralysis C0023176 Lead poisoning MalaCards C0751837 Gait ataxic C2749862 Mitochondrial neurogastrointestinal encephalopathy syndrome, rrm2b-related HPO C1836296 Lower extremity weakness C1853554 Radiation induced meningioma MalaCards C4084775 Usual severity weight loss C0021845 Intestinal perforation HSDN C4084767 Bothered by vomiting C0085298 Sudden cardiac death HSDN C0221263 Cafe au lait spot C0175704 Leopard syndrome HPO C1963091 Diarrhea adverse event C0011615 Dermatitis, atopic HSDN C2984057 Have nausea C0027809 Neurilemmoma HSDN C2203646 Jaundice C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO C0015230 Exanthem C0008728 Churg-strauss syndrome OrphaNet|MalaCards C0557874 Global developmental delay C3150941 Rubinstein-taybi syndrome 2 MalaCards|HPO C4084802 Usual severity diarrhea C0041316 Lymph node tuberculosis HSDN C3146279 Coma C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C1549543 Administration method - pain C0036420 Localized scleroderma HSDN C0221232 Welts C0272203 Indolent systemic mastocytosis UMLS C1963071 Back pain adverse event C0022665 Kidney neoplasm HSDN C1557397 Adverse event associated with pain C0344423 Atrial flutter by ecg finding HSDN C0018681 Headache, cephalalgia C1000483 Genus anemia HSDN C4085210 Usual severity pain C0039236 Tachycardia episodic HSDN C0013421 Dystonia C0032965 Pregnancy complications, infectious HSDN C4084802 Usual severity diarrhea C0032087 Plant poisoning HSDN C0020455 Hypergammaglobulinemia C0019194 Animal viral hepatitis HSDN C0042024 Urine incontinence C0010346 Crohn disease HSDN C0040034 Thrombocytopenia C1835916 Aicardi-goutieres syndrome 3 MalaCards|HPO C0344315 Mood depressed C0030567 Parkinson disease MalaCards C0019079 Bloody sputum C0035238 Congenital abnormality of respiratory system HSDN C0086437 Joint hypermobility C0796012 Krause-kivlin syndrome HPO C0020455 Hypergammaglobulinemia C0268381 Primary amyloidosis OrphaNet C0424755 Fever symptoms C0036344 Schizophrenia, catatonic HSDN C1263846 Attention deficit disorder with hyperactivity C0917800 Epilepsy, myoclonic, infantile OrphaNet|MalaCards C4084775 Usual severity weight loss C0002395 Alzheimer's disease HSDN C0015672 Decreased energy C0015457 Expression facial HSDN C4084775 Usual severity weight loss C0037929 Spinal cord injuries HSDN C0036572 Convulsion C0033953 Psychosexual disorders HSDN C0917816 Deficiency mental C3150730 Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency HPO C0010200 Cough symptom C0024530 Malaria HSDN C3203358 Alveolar hypoventilation C0026850 Muscular dystrophy HSDN C2237041 Shox gene with short stature C1839735 Miles-carpenter x-linked mental retardation syndrome MalaCards C0015469 Facial paralysis C0019159 Hepatitis a HSDN C0237326 Defecation pain C0013364 Dysautonomia, familial HPO C0030193 Sense of pain C0741026 Angina atypical UMLS C0009460 Communication impairment C0004936 Mental disorders HSDN C0030193 Sense of pain C0019202 Hepatolenticular degeneration HSDN C1384666 Decreased hearing C0026896 Myasthenia gravis MalaCards|HSDN C3539023 Pelvic pain increasing in frequency C0085096 Peripheral vascular diseases HSDN C0030193 Sense of pain C0030528 Paratyphoid fever HSDN C2024878 Cardiovascular surgery result: dyspnea C0037769 West syndrome HPO C0242936 Center pain C1861172 Venous thromboembolism HSDN C0024312 Lymphocytopenia C2936664 Acquired hypogammaglobulinemia MalaCards C0424755 Fever symptoms C0040053 Thrombosis HSDN C0851578 Disorder sleep C0005591 Avian disease HSDN C4084769 Vomiting frequency C1636667 Disorder characterized by eosinophilia HSDN C0013404 Respiratory difficulty C1848947 Cold-induced sweating syndrome 1 HPO|UMLS C4084784 Diarrhea C0585274 Periodic syndrome OrphaNet|HPO C2984058 Have pain C0013884 Filarial elephantiases HSDN C1963281 Vomiting adverse event C0020428 Hyperaldosteronism HSDN C4084723 Constipation C0033247 Proctocolitis HSDN C2984057 Have nausea C0032966 Complication, neoplastic pregnancy HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162790 Harassment sexual HSDN C0018681 Headache, cephalalgia C1963084 Colitis adverse event HSDN C1963090 Dehydration adverse event C0043398 Yellow fever, urban MalaCards C0018681 Headache, cephalalgia C1762616 Meningioma, benign, no icd-o subtype MalaCards C0039070 Collapse fleeting C0003490 Aortic arch syndrome HSDN C1963093 Dizziness adverse event C0022116 Ischemia HSDN C0751495 Seizure focal C0149958 Complex partial seizures UMLS C4084775 Usual severity weight loss C0036864 Sexual relations HSDN C0002170 Alopecia disorders C1721007 Pachyonychia congenita, type 2 (disorder) MalaCards C0042798 Vision dim C2931795 Chromosome 11, deletion 11p OrphaNet C0005745 Blepharoptosis C1851879 Cleft lip with or without cleft palate, nonsyndromic, 8 HPO C0085631 Abnormal excitement C1421293 Ube3a gene HSDN C1384666 Decreased hearing C1844853 Brachytelephalangic chondrodysplasia punctata HPO C0000727 Abdomen acute C0011649 Dermoid cyst HSDN C0242936 Center pain C0020120 Engineering humans HSDN C3641756 Have diarrhea C0035613 Rift valley fever OrphaNet|MalaCards C0022346 Yellow skin C2981669 Stage iv distal bile duct cancer UMLS C1527344 Dysphonia C0035468 Scleroma HSDN C0004604 Pain back C0007138 Carcinoma, transitional cell HSDN C2203646 Jaundice C0018767 Auditory sense HSDN C0042940 Disorder of voice C0035468 Scleroma HSDN C4084773 Bothered by weight gain C0026266 Mitral valve insufficiency HSDN C0015970 Fever unknown origin C0026640 Mouth neoplasms HSDN C0024031 Back pain lower back C0022758 Kap HSDN C4084788 Have dizziness C0025427 Mercury poisoning HSDN C0034150 Skin purpura C0019841 Classical swine fever HSDN C0221166 Paraparesis C1145628 Autonomic nervous system disorders HSDN C2024878 Cardiovascular surgery result: dyspnea C0007820 Cerebrovascular disorders HSDN C0036572 Convulsion C0016667 Fragile x syndrome MalaCards|HSDN|HPO|UMLS C0004604 Pain back C0029442 Osteomalacia HSDN C4085211 Pain distress question C0033927 Psychopathology HSDN C4020887 Photodysphoria C3665333 Keratitis-ichthyosis-deafness syndrome OrphaNet|HPO|MalaCards C0010038 Corneal opacity disorder C2930808 Familial vascular leukoencephalopathy MalaCards C4085211 Pain distress question C0028738 Nystagmus HSDN C0032617 High urine output C0395005 Psychogenic polydipsia UMLS C0155552 Hearing loss mixed C0344311 Blister HSDN C4084773 Bothered by weight gain C1956257 Pulmonary stenosis HSDN C3829611 Nausea frequency C0018188 Granuloma HSDN C1963137 Hydrocephalus adverse event C0265240 Goldenhar syndrome MalaCards C0033774 Skin pruritus C0019100 Severe dengue OrphaNet C2984058 Have pain C0023485 Precursor b-cell lymphoblastic leukemia-lymphoma HSDN C0013404 Respiratory difficulty C2973725 Pulmonary arterial hypertension OrphaNet C0022346 Yellow skin C0035243 Respiratory tract infections HSDN C4085211 Pain distress question C0036130 Salpingitis HSDN C4084776 Weight loss C0025521 Inborn errors of metabolism HSDN C4084723 Constipation C0034530 Injury radiation HSDN C4085222 Nausea C0027809 Neurilemmoma HSDN C0026858 Musculoskeletal pain C0027121 Myositis HSDN C4084773 Bothered by weight gain C0022658 Kidney diseases HSDN C0003910 Articulation disorder C0016719 Friedreich ataxia HSDN C0039070 Collapse fleeting C0008628 Chromosome deletion HSDN C0557874 Global developmental delay C0431399 Familial aplasia of the vermis MalaCards|HPO C0027066 Myoclonic jerking C0015423 Eyelid diseases HSDN C0851578 Disorder sleep C0524910 Hepatitis c, chronic HSDN C4085211 Pain distress question C0014461 Granuloma eosinophilic HSDN C4084768 Usual severity vomiting C0020542 Pulmonary hypertension HSDN C4085548 Usual severity dizziness C0342257 Complications of diabetes mellitus HSDN C0042963 Symptoms vomiting C0027819 Neuroblastoma HSDN C1961131 Cough adverse event C0348018 Projections HSDN C0042940 Disorder of voice C0020701 Somatization disorder HSDN C0019079 Bloody sputum C0007786 Brain ischemia HSDN C0011206 Delirium acute C0003962 Ascites HSDN C0151686 Growth retardation C3280766 Joubert syndrome 14 MalaCards C3815497 Cough C0014858 Esophageal motility disorders HSDN C0015672 Decreased energy C0020517 Hypersensitivity HSDN C0851578 Disorder sleep C0022660 Kidney failure, acute HSDN C0002962 Angina C0028242 Nocardia infections HSDN C0003550 Broca aphasia C0344315 Depressed mood HSDN C0030975 Disorders perception C0525045 Mood disorders HSDN C4084767 Bothered by vomiting C0040997 Trigeminal neuralgia HSDN C0009806 Constipate C2677303 Diastasis recti and weakness of the linea alba UMLS C0018780 Frequencies hearing high loss C2137063 Ent surgical result - speech HSDN C1963071 Back pain adverse event C0031154 Peritonitis HSDN C0013362 Dysarthrias C0220765 Weaver-like syndrome MalaCards|HPO C0424755 Fever symptoms C0282312 Bubonic plague DiseaseOntology|MalaCards C0042755 Virilisation C0021359 Infertility HSDN C0036572 Convulsion C0018553 Hamartoma syndrome, multiple MalaCards|HPO|UMLS C3274924 Have been coughing C0026636 Mouth diseases HSDN C0851578 Disorder sleep C0004114 Astrocytoma HSDN C4084767 Bothered by vomiting C0040247 Tinea HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0027626 Neoplasm invasiveness HSDN C0233844 Awkwardness C0024408 Machado-joseph disease OrphaNet|MalaCards C0004604 Pain back C0014544 Epilepsy HSDN C0004134 Dyssynergia C0679360 Foodborne disease HSDN C0454644 Delayed language development C0342783 Deficiency of butyryl-coa dehydrogenase MalaCards|HPO C0042798 Vision dim C3554592 Mcopcb9 MalaCards C0035078 Failure kidney C2673610 Jeb-i MalaCards C0039070 Collapse fleeting C0015726 Focused anxiety HSDN C0007859 Pain neck C0949691 Spondylarthropathies HSDN C0039070 Collapse fleeting C0403447 Chronic kidney insufficiency UMLS C0332563 Papulae C0085652 Pyoderma gangrenosum OrphaNet|MalaCards C4084723 Constipation C0015663 Fasting HSDN C0007758 Cerebellar ataxia C3164344 Adult onset autosomal dominant leukodystrophy OrphaNet|HPO C3539023 Pelvic pain increasing in frequency C0038160 Staphylococcal infections HSDN C0000737 Abdomen pain C2062326 Eosinophilic enteropathy OrphaNet|MalaCards C0413252 Hypothermia due to exposure C0036344 Schizophrenia, catatonic HSDN C2919142 Short stature adverse event C2931850 Aase smith syndrome 2 MalaCards|HPO C0851578 Disorder sleep C0018021 Goiter HSDN C1961131 Cough adverse event C0036117 Salmonella infections HSDN C1557397 Adverse event associated with pain C0030318 Panic state HSDN C0030554 Abnormal sensation C0020550 Hyperthyroidism HSDN C1963281 Vomiting adverse event C1832736 Congenital disorder of glycosylation, type id MalaCards|HPO C0019521 Hiccoughs C0012746 Dissociative disorder HSDN C4084784 Diarrhea C0042870 Vitamin d deficiency HSDN C1963090 Dehydration adverse event C0010674 Cystic fibrosis MalaCards|HPO C0030486 Extremity paralysis, lower C0023343 Leprosy HSDN C4085210 Usual severity pain C2350521 Gustatory perception HSDN C0151889 Reflexes tendon increased C1849140 Spastic ataxia, charlevoix-saguenay type MalaCards|HPO C4084723 Constipation C0162809 Kallmann syndrome HPO C1319543 On examination - right eye diabetic maculopathy C0339471 Diabetic maculopathy UMLS C1000483 Genus anemia C0024530 Malaria OrphaNet|MalaCards C0018784 Deafness sensorineural C0085423 Gram-negative bacterial infections HSDN C2096293 Ent surgical result ear vertigo C2984572 Malaria pathway HSDN C0011991 Loose stools C0024236 Lymphedema HSDN C0019825 Voice hoarseness C2004491 Cicatrix HSDN C0004134 Dyssynergia C0265965 Dyskeratosis congenita MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0036095 Salivary gland neoplasms HSDN C3887873 Hearing loss C0006277 Bronchitis HSDN C0242936 Center pain C0016879 Fusobacterium infections HSDN C0011168 Disorder deglutition C1846331 Juvenile-onset dystonia MalaCards C1963137 Hydrocephalus adverse event C1961835 Gaucher disease, type 1 MalaCards C0019825 Voice hoarseness C2137063 Ent surgical result - speech HSDN C4084775 Usual severity weight loss C0017563 Gingival diseases HSDN C1557397 Adverse event associated with pain C0036239 Satiety HSDN C0032617 High urine output C0011570 Mental depression HSDN C0042963 Symptoms vomiting C3888018 Congenital hyperinsulinism MalaCards C0002962 Angina C0022362 Jaw diseases HSDN C0033377 Caudal displacement C3711749 Nonsyndromic holoprosencephaly MalaCards C0013395 Indigestion C0010709 Cyst HSDN C1549543 Administration method - pain C0040441 Broken teeth HSDN C1549543 Administration method - pain C0035008 Reinforcement schedules HSDN C3887638 Failure to thrive in infant C0041296 Tuberculosis HSDN C4084802 Usual severity diarrhea C1704421 Skin pigmentation disorder HSDN C0018681 Headache, cephalalgia C0022660 Kidney failure, acute HSDN C0038990 Sweats C1854961 Lisker garcia ramos syndrome MalaCards C0018681 Headache, cephalalgia C0018235 Aggrieved HSDN C0750394 Wbc low C0011989 Camurati-engelmann syndrome MalaCards|HPO C0039070 Collapse fleeting C0314657 Genetic predisposition HSDN C0027497 Queasy C0002991 Cutaneous fibrous histiocytoma HSDN C0019572 Hairiness C1579931 Depressed - symptom HSDN C4084774 Have weight loss C0517555 Venous thrombosis after immobility HSDN C0085606 Urination urgency C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C0000737 Abdomen pain C0702166 Acne HSDN C0009676 Confusion state C0017636 Glioblastoma HSDN C0009398 Color vision defects C1864877 Csnb, incomplete, autosomal recessive MalaCards|HPO C0026821 Cramp C0009946 Conversion disorder HSDN C0015672 Decreased energy C0393819 Polyradiculoneuropathy, chronic inflammatory demyelinating HSDN C2032396 Pelvic pain on the right C2586211 Thrombosis of blood vessel HSDN C4084897 Sleep disturbance subordinate domain C0001231 Acth syndrome, ectopic MalaCards C0013404 Respiratory difficulty C0023804 Lipomatosis, multiple symmetrical HSDN C2132198 Abnormal blistering of the skin C2242987 Benign mastocytoma MalaCards C4085210 Usual severity pain C0021846 Intestinal polyps HSDN C4084776 Weight loss C0029001 Onchocerciasis HSDN C4085317 Diarrhea frequency C1005359 Pica pica bird HSDN C0917816 Deficiency mental C0796020 Lowry-maclean syndrome MalaCards C3541349 Syncope C0023055 Laryngeal neoplasm HSDN C0474368 Childbirth pain C0436596 On examination - apathetic HSDN C0018681 Headache, cephalalgia C0496842 Malignant neoplasm of pituitary gland MalaCards C3665347 Vision impaired C1848561 Methylmalonic acidemia with homocystinuria MalaCards|HPO C0043094 Weight gain C0034063 Pulmonary edema HSDN C0013604 Edematous C0036117 Salmonella infections HSDN C1549543 Administration method - pain C0009480 Community psychiatry HSDN C0018772 Deafness C0003708 Arachnitis OrphaNet|MalaCards C0349588 Stature short C2931597 Macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance MalaCards C4084766 Vomiting C0024667 Animal mammary neoplasms HSDN C0010200 Cough symptom C1457883 Aggressive reaction HSDN C0018991 Paralysis one side of body C0016399 Seizure focal motor HSDN C1557397 Adverse event associated with pain C0023869 Lithiasis HSDN C0002962 Angina C0015695 Fatty liver HSDN C3463815 Feel fatigue C0034063 Pulmonary edema HSDN C4085317 Diarrhea frequency C0028768 Obsessive-compulsive disorder HSDN C0043094 Weight gain C0016563 Form perception HSDN C0040264 Ear ringing sound C0997768 Glaucoma HSDN C4084727 Cough frequency C0010823 Cytomegalovirus infections HSDN C2203646 Jaundice C0037361 Olfactory sense HSDN C4085210 Usual severity pain C0017572 Gingival recession HSDN C0019825 Voice hoarseness C0342853 Sialuria OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0752138 Intracranial arterial diseases HSDN C4085317 Diarrhea frequency C0026780 Mumps HSDN C0232462 Appetite decrease C1836327 Rhabdoid tumor predisposition syndrome 1 (disorder) MalaCards C4042891 Sleep wake disorders C0006012 Borderline personality disorder HSDN C2911647 Weight gain adverse event C0036117 Salmonella infections HSDN C0013421 Dystonia C0006663 Calcinosis HSDN C3641756 Have diarrhea C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C1549543 Administration method - pain C1419157 Pygm gene HSDN C0015672 Decreased energy C0001314 Acute disease HSDN C4084768 Usual severity vomiting C0080178 Spina bifida HSDN C0030193 Sense of pain C0264677 Angina class iii UMLS C1145670 Failure respiratory C2931220 Symmetrical infantile thalamic degeneration OrphaNet C4084767 Bothered by vomiting C0007570 Celiac disease HSDN C0232466 Feeding difficulty C0406727 Orofaciodigital syndrome 4 MalaCards C0040822 D tremors C0206247 Amyloid neuropathies MalaCards C0085636 Light sensitivity C0268506 Albinoidism MalaCards C4084723 Constipation C2911243 Encounter due to family history of colonic polyps HSDN C4085211 Pain distress question C0029422 Osteochondrodysplasias HSDN C1962972 Proteinuria adverse event C0038525 Subarachnoid hemorrhage HSDN C0221752 Rbc urine C0342750 Glycogen storage disease type id MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C3151209 Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome HPO C1090821 Sepsis C0221023 Cyclic neutropenia OrphaNet|HPO C4049644 Depression C0175702 Williams syndrome OrphaNet|HPO|MalaCards C3898969 Have been vomiting C0007787 Transient ischemic attack HSDN C0018772 Deafness C0018965 Hematuria HSDN C0454644 Delayed language development C1968551 Mental retardation, x-linked 79 MalaCards|HPO C0015970 Fever unknown origin C2239176 Liver carcinoma HSDN C0007859 Pain neck C0752155 Central nervous system vascular malformations HSDN C0547030 Sensory perceptual alteration: visual C0242225 Color blindness UMLS C4084802 Usual severity diarrhea C2937287 Hematolysis HSDN C0424755 Fever symptoms C0015671 Father HSDN C1145670 Failure respiratory C0265334 Pachyonychia congenita MalaCards|HPO C0000737 Abdomen pain C2348737 Gastric mixed adenocarcinoma UMLS C4085222 Nausea C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C1963091 Diarrhea adverse event C4084971 Trachoma HSDN C0013608 Cardiac edema C0031046 Pericarditis HSDN C0018784 Deafness sensorineural C1843852 Spinocerebellar ataxia with epilepsy HPO C1963252 Tremor adverse event C0007786 Brain ischemia HSDN C0162298 Stiffness joints C1859312 Camfak syndrome OrphaNet|HPO C0518090 Frequency of pain question C0282507 Heat stress disorders HSDN C0030552 Paralysis partial C1269683 Major depressive disorder HSDN C1263846 Attention deficit disorder with hyperactivity C0175694 Smith-lemli-opitz syndrome OrphaNet|HPO|MalaCards C2984058 Have pain C0517555 Venous thrombosis after immobility HSDN C4042891 Sleep wake disorders C0001122 Acidosis HSDN C4084776 Weight loss C0027412 Opioid-related disorders HSDN C0042963 Symptoms vomiting C0017601 Glaucomas HSDN C0030193 Sense of pain C0001486 Adenovirus infections HSDN C1961131 Cough adverse event C0032131 Plasmacytoma HSDN C1565249 Limitation, mobility C0521169 Fracture compression HSDN C0349588 Stature short C0265497 Chromosome xxxxx syndrome OrphaNet|MalaCards C3541349 Syncope C0021818 Intervertebral disk displacement HSDN C0812426 Kidney problem C0746843 Nephrostomy tube obstructed UMLS C0013362 Dysarthrias C0085315 Toxoplasmosis, cerebral HSDN C0018681 Headache, cephalalgia C1332949 Childhood brain meningioma UMLS C4085642 Level of joint stiffness C0300948 Caudal regression syndrome OrphaNet|HPO C4084723 Constipation C1864648 Chromosome 16p13.3 deletion syndrome, proximal MalaCards C1963249 Tinnitus adverse event C0003708 Arachnitis OrphaNet|MalaCards C3463815 Feel fatigue C0007820 Cerebrovascular disorders HSDN C0013604 Edematous C0007125 Carcinoma, ehrlich tumor HSDN C1963091 Diarrhea adverse event C0026782 Mumps vaccine HSDN C4084775 Usual severity weight loss C0023051 Laryngeal diseases HSDN C1069915 Vertigo C0038019 Spondylosis HSDN C0020580 Decreased sensation C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0008031 Pain chest C0242875 Ventricular septal rupture HSDN C2017159 Left leg soft tissue swelling extending to the ankle C0037580 Soft tissue swelling UMLS C0030552 Paralysis partial C0035304 Retinal degeneration HSDN C0521763 Nystagmus produced by neck rotation C0015397 Disorder of eye UMLS C4085211 Pain distress question C0221002 Hyperparathyroidism, primary HSDN C0917801 Sleep disorder insomnia C0497327 Dementia UMLS C3494358 Characteristic, prodromal C1579931 Depressed - symptom HSDN C3898969 Have been vomiting C0348018 Projections HSDN C3539893 Pelvic pain occurs with intercourse C0206630 Endometrial stromal sarcoma HSDN C0042571 Vertigo subjective C0019562 Von hippel-lindau syndrome MalaCards|HSDN|HPO|UMLS C3665347 Vision impaired C0796070 Microphthalmia, syndromic 7 MalaCards C0454644 Delayed language development C1970196 Mental retardation, autosomal recessive 8 MalaCards C0030193 Sense of pain C0238461 Anaplastic thyroid carcinoma OrphaNet C0002962 Angina C0010709 Cyst HSDN C4084769 Vomiting frequency C0268412 Infantile hypophosphatasia MalaCards|HPO C0015469 Facial paralysis C0270968 Limb-girdle muscular dystrophy type 2h MalaCards|HPO C0042571 Vertigo subjective C0022661 Kidney failure, chronic HSDN C0042571 Vertigo subjective C0001883 Airway obstruction HSDN C0349588 Stature short C0265223 Cohen syndrome OrphaNet|HPO C1557397 Adverse event associated with pain C3540680 Nci ctep sdc mastocytosis sub-category terminology HSDN C0040259 Tinea pedis C0007137 Squamous cell carcinoma HSDN C0030552 Paralysis partial C0027643 Neoplasm recurrence, local HSDN C1768507 Yellow nails C0346104 Follicular atrophoderma and basal cell epitheliomata OrphaNet|MalaCards C0013604 Edematous C0016398 Focal infection, dental HSDN C0241165 Skin thickening C0022595 Keratosis follicularis OrphaNet C0237326 Defecation pain C1868512 Leukodystrophy, demyelinating, adult-onset, autosomal dominant OrphaNet|HPO C0031315 Phantom limb pain C0001175 Acquired immunodeficiency syndrome HSDN C2096293 Ent surgical result ear vertigo C0027686 Pathologic neovascularization HSDN C0232466 Feeding difficulty C0546264 Congenital fiber type disproportion HPO C4084724 Usual severity constipation C1962986 Glaucoma adverse event HSDN C4084788 Have dizziness C0006818 Campylobacter infection HSDN C4085661 Usual severity nausea C0024841 Matrimony, matrimonial HSDN C0018784 Deafness sensorineural C0008297 Choanal atresia HSDN C0033377 Caudal displacement C0242387 Mandibulofacial dysostosis MalaCards|HPO C4085210 Usual severity pain C0019151 Hepatic encephalopathy HSDN C2315100 Pediatric failure to thrive C1864499 Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss HPO C3539891 Pelvic pain to the rear C1547940 Specimen source codes - ulcer HSDN C0028081 Night sweat C0032285 Pneumonia UMLS C0030193 Sense of pain C0022650 Kidney calculi HSDN C0004134 Dyssynergia C2706915 Language:-:point in time:^patient:- HSDN C0010200 Cough symptom C0497327 Dementia HSDN C0751265 Learning disability C0795907 Conotruncal anomaly face syndrome MalaCards C0004134 Dyssynergia C1868311 Piebald trait neurologic defects OrphaNet|MalaCards C0003113 Anomia C0004782 Basal ganglia diseases HSDN C0010200 Cough symptom C0025061 Disease of mediastinum HSDN C0522224 Palsied C0018051 Gonadal dysgenesis HSDN C2911645 Weight loss adverse event C0008533 Hemophilia b HSDN C2919142 Short stature adverse event C3280355 Chromosome 15q25 deletion syndrome MalaCards C4084776 Weight loss C0018133 Graft-vs-host disease HSDN C1557397 Adverse event associated with pain C0036986 Shock, traumatic HSDN C1963252 Tremor adverse event C0439840 Reflex motion descriptor HSDN C0013404 Respiratory difficulty C0025303 Meningococcal infections HSDN C4085862 Bothered by nausea C0017181 Gastrointestinal hemorrhage HSDN C0018772 Deafness C0085426 Gram-positive bacterial infections HSDN C0015468 Face pain C0016130 Finger sucking HSDN C1963091 Diarrhea adverse event C0342287 Thiamine responsive megaloblastic anemia syndrome OrphaNet|HPO|MalaCards C0234378 Postural tremor C4225336 Dystonia 27 UMLS C3146279 Coma C0920350 Autoimmune thyroiditis HSDN C0019209 Large liver C0085132 Mucopolysaccharidosis vii HPO C0221166 Paraparesis C0752342 Neuroaspergillosis HSDN C2029884 Hearing loss by exam C0028738 Nystagmus HSDN C0015672 Decreased energy C0497327 Dementia HSDN C0000737 Abdomen pain C0016124 Finger injury HSDN C1963170 Hypothermia adverse event C0013182 Drug allergy HSDN C0522224 Palsied C0020473 Hyperlipidemia HSDN C0036572 Convulsion C3814530 Skin vesicle HSDN C0030486 Extremity paralysis, lower C0004161 Athletic injuries HSDN C0010038 Corneal opacity disorder C1704421 Skin pigmentation disorder MalaCards C0018681 Headache, cephalalgia C0524910 Hepatitis c, chronic HSDN C1579931 Depressed - symptom C0795953 Masa syndrome (disorder) MalaCards C4084766 Vomiting C1536500 Deficiency of acetyl-coa acetyltransferase MalaCards|HPO C1145670 Failure respiratory C1510479 Neuralgic amyotrophy MalaCards|HPO C0242936 Center pain C0020757 Ichthyoses HSDN C0557874 Global developmental delay C2750068 Roifman-chitayat syndrome MalaCards C4085317 Diarrhea frequency C0027831 Neurofibromatosis 1 HSDN C0020455 Hypergammaglobulinemia C0040100 Thymoma HSDN C0042798 Vision dim C1842362 Hermansky-pudlak syndrome 2 MalaCards|HPO C0042940 Disorder of voice C1579931 Depressed - symptom HSDN C0162285 Edema eyelid C1859228 Cerebrohepatorenal syndrome, variant types HPO C0042024 Urine incontinence C0020179 Huntington disease HSDN C0009806 Constipate C0017638 Glioma HSDN C2024893 Cardiovascular surgery result: fatigue C0000735 Abdominal neoplasms HSDN C0013421 Dystonia C0038661 Suicide HSDN C0018772 Deafness C0268680 Biotin deficiency MalaCards C4085211 Pain distress question C0338480 Common migraine HSDN C4084768 Usual severity vomiting C0268328 Porphobilinogen synthase deficiency MalaCards|HPO C1565249 Limitation, mobility C0158266 Intervertebral disc degeneration HSDN C0151311 Cranial nerve palsy C0206641 Osteochondromatosis OrphaNet|HPO C2024878 Cardiovascular surgery result: dyspnea C1837218 Cleft palate, isolated HSDN C3829611 Nausea frequency C0022661 Kidney failure, chronic HSDN C1549543 Administration method - pain C0221056 Adult type dermatomyositis HSDN C4084774 Have weight loss C0024530 Malaria HSDN C1963071 Back pain adverse event C0035956 Rupture spontaneous HSDN C0085593 Chill C0031154 Peritonitis HSDN C0043094 Weight gain C0016053 Fibromyalgia HSDN C4084724 Usual severity constipation C0016470 Food allergy HSDN C4084775 Usual severity weight loss C0010414 Infection by cryptococcus neoformans HSDN C4084766 Vomiting C1622510 Neurocytoma HSDN C1549543 Administration method - pain C0002950 Aneurysms inflammatory HSDN C0013395 Indigestion C0853697 Neutrophil count decreased HSDN C0009806 Constipate C0001807 Aggressive behavior HSDN C3539023 Pelvic pain increasing in frequency C0009324 Ulcerative colitis HSDN C2984058 Have pain C0024537 Malaria, vivax HSDN C4084802 Usual severity diarrhea C1833275 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative HPO C0013362 Dysarthrias C0751918 Cockayne pelizaeus merzbacher disease MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0008924 Cleft lip HSDN C0234376 Tremor action C1842534 Dystonia 18 (disorder) MalaCards|UMLS C0522224 Palsied C0009375 Colonic neoplasms HSDN C3665492 Pigmentations C0007130 Mucinous adenocarcinoma MalaCards C0011991 Loose stools C0042076 Urologic neoplasms HSDN C2127434 Bilateral leg paralysis C0030486 Paraplegia UMLS C0026838 Spasticity muscle C0043346 Xeroderma pigmentosum MalaCards|HPO C4085210 Usual severity pain C0015395 Burn eye HSDN C0232466 Feeding difficulty C2749861 Mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) MalaCards|HPO C2919142 Short stature adverse event C0023374 Lesch-nyhan syndrome MalaCards|HPO C0042963 Symptoms vomiting C0024228 Lymphatic diseases HSDN C2029884 Hearing loss by exam C1704212 Embolism embolus HSDN C0029163 Hemorrhage mouth C0852077 Blood coagulation disorders, inherited HSDN C0018772 Deafness C0004936 Mental disorders HSDN C0033377 Caudal displacement C2931578 Bassoe syndrome OrphaNet|MalaCards C0018681 Headache, cephalalgia C1962963 Osteoporosis adverse event HSDN C3641756 Have diarrhea C0242172 Pelvic inflammatory disease HSDN C0727671 Red cross toothache drops C0004096 Asthma HSDN C1962972 Proteinuria adverse event C0334419 Pheochromocytoma, malignant MalaCards C0013404 Respiratory difficulty C0852283 Respiratory distress syndrome MalaCards C0349588 Stature short C3554446 Brachydactyly, type a1, c MalaCards C0004134 Dyssynergia C0026613 Motor skills disorders HSDN C2169806 Tic C0004096 Asthma HSDN C4085211 Pain distress question C0024440 Macular edema, cystoid HSDN C0574941 Inflamed joint C2316212 Cryopyrin-associated periodic syndromes MalaCards C2203646 Jaundice C0040156 Thyrotoxicosis HSDN C0043094 Weight gain C0850803 Anaphylaxis (non medication) HSDN C0013404 Respiratory difficulty C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4085661 Usual severity nausea C2586211 Thrombosis of blood vessel HSDN C0013404 Respiratory difficulty C0585442 Osteosarcoma of bone HSDN C4085642 Level of joint stiffness C4014722 Sting-associated vasculopathy, infantile-onset MalaCards C2315100 Pediatric failure to thrive C1275081 Cardio-facio-cutaneous syndrome HPO C0035229 Respiratory function impaired C0795947 Fryns-van den berghe syndrome OrphaNet|MalaCards C2911647 Weight gain adverse event C0562691 Herbivores HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0009373 Colonic diseases HSDN C0018991 Paralysis one side of body C0019080 Hemorrhage HSDN C1963137 Hydrocephalus adverse event C2931557 Chromosome 4 short arm deletion MalaCards C1963252 Tremor adverse event C0035243 Respiratory tract infections HSDN C2024878 Cardiovascular surgery result: dyspnea C0085084 Motor neuron disease HSDN C0004134 Dyssynergia C1145628 Autonomic nervous system disorders HSDN C1963090 Dehydration adverse event C1855102 Methylmalonic aciduria cblb type HPO C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0700327 Clinical findings relating to memory HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C3658239 D personality, type HSDN C4084802 Usual severity diarrhea C0005745 Blepharoptosis HSDN C1549543 Administration method - pain C0018566 Congenital hand deformities HSDN C0151786 Weakness muscle C0393593 Dystonia disorders HSDN C4085549 Dizziness C0039263 Takayasu arteritis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C1546847 Entity name part type - family HSDN C2024893 Cardiovascular surgery result: fatigue C3539923 Cdisc adas-cog - orientation summary score HSDN C0028738 Nystagmus C0796117 Pitt syndrome MalaCards C4085210 Usual severity pain C3827868 Tachycardia by ecg finding HSDN C2919142 Short stature adverse event C0023003 Langer-giedion syndrome OrphaNet|HPO|MalaCards C0023012 Delay language C2750234 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 MalaCards|HPO C0018775 Hearing loss bilateral C0004943 Behcet syndrome HSDN C1963184 Nystagmus adverse event C1845446 Corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia OrphaNet|HPO C0744798 Hemoptysis occasional C0740767 Resp_tract problem UMLS C0242936 Center pain C0553716 Uterine prolapse without mention of vaginal wall prolapse HSDN C0151786 Weakness muscle C0042138 Uterine neoplasms HSDN C0018681 Headache, cephalalgia C0042376 Vascular headaches UMLS C2984058 Have pain C0029888 Otitis media purulent HSDN C1549543 Administration method - pain C2240374 Eosinophil count raised HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0023530 Leukopenia HSDN C2024878 Cardiovascular surgery result: dyspnea C2931642 Benign symmetrical lipomatosis HSDN C0086565 Liver function abnormal C1856127 Bile acid synthesis defect, congenital, 2 OrphaNet|HPO|MalaCards C2315100 Pediatric failure to thrive C2931001 Congenital disorder of glycosylation type 1g MalaCards C4084776 Weight loss C2931785 Juvenile dermatomyositis MalaCards C0577564 Mass of lymphoreticular structure C0686539 Burkitt's tumor of unspecified, extranodal, or solid organ site UMLS C4085317 Diarrhea frequency C0037930 Spinal cord neoplasms HSDN C2984057 Have nausea C2827407 Infectious otitis media HSDN C3539889 Pelvic pain increasing in severity C0458219 Complex regional pain syndromes HSDN C2911647 Weight gain adverse event C1258104 Diffuse scleroderma HSDN C0018772 Deafness C1856871 Aarskog-like syndrome MalaCards C3641756 Have diarrhea C2020541 Strabismus HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0017636 Glioblastoma HSDN C0011991 Loose stools C0002171 Alopecia areata HSDN C0033774 Skin pruritus C0037278 Skin diseases, infectious HSDN C4085211 Pain distress question C0006266 Bronchial spasm HSDN C0011991 Loose stools C0007125 Carcinoma, ehrlich tumor HSDN C4084727 Cough frequency C0524688 Pneumonic plague DiseaseOntology|MalaCards C2984058 Have pain C0035229 Respiratory insufficiency HSDN C0004134 Dyssynergia C0042514 Tachycardia, ventricular HSDN C1963091 Diarrhea adverse event C0025064 Mediastinitis HSDN C0018784 Deafness sensorineural C2750784 Spastic paraplegia 44, autosomal recessive (disorder) MalaCards|HPO C2911645 Weight loss adverse event C0015927 Intrauterine fetal demise HSDN C1959630 Eye pain adverse event C0017653 Glomus tumor HSDN C0332573 Macula C2242987 Benign mastocytoma MalaCards C1963071 Back pain adverse event C0037051 Behavior illness HSDN C4085317 Diarrhea frequency C0424688 Small head HSDN C0037316 Not enough sleeping C0031212 Personality disorders HSDN C0424755 Fever symptoms C0013370 Amebic colitis HSDN C0018681 Headache, cephalalgia C0028738 Nystagmus HSDN C0042798 Vision dim C0036677 Sensory threshold HSDN C4085210 Usual severity pain C0006736 Body stone HSDN C4084802 Usual severity diarrhea C0206255 Malaria vaccine HSDN C0150055 Pain chronic C0237873 Physiological sexual disorders HSDN C4085222 Nausea C0036875 Disorders of sex development HSDN C0012569 Double vision C0014549 Tonic-clonic epilepsy HSDN C4085317 Diarrhea frequency C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C0013362 Dysarthrias C1834014 Oculopharyngodistal myopathy MalaCards C0010038 Corneal opacity disorder C0238286 Mucolipidosis type iv OrphaNet|HPO|MalaCards C0015938 Fetal macrosomia C0019693 Hiv infections HSDN C0010200 Cough symptom C2073625 X-ray of chest: pleural effusion HSDN C0151889 Reflexes tendon increased C3472711 Spinocerebellar ataxia 36 MalaCards C0018681 Headache, cephalalgia C0003855 Arteriovenous fistula HSDN C0039870 Leanness C0011581 Depressive disorder HSDN C0015469 Facial paralysis C0517555 Venous thrombosis after immobility HSDN C0398650 Idiopathic thrombocytopenia purpura C0005695 Bladder neoplasm HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0006267 Bronchiectasis HSDN C0085610 Bradycardia sinus C1834144 Sick sinus syndrome 2, autosomal dominant MalaCards|HPO C1963093 Dizziness adverse event C0013010 Cerebral lateralization HSDN C3887873 Hearing loss C2698658 Orofaciodigital syndrome type 1 MalaCards C0020649 Blood pressure decreased C3164344 Adult onset autosomal dominant leukodystrophy OrphaNet|HPO C0234146 Absent reflex C3150801 Combined oxidative phosphorylation deficiency 7 MalaCards|HPO C0231218 Malaise generalized C2828210 Stage ia pleural mesothelioma UMLS C3539022 Pelvic pain decreasing in severity C0022661 Kidney failure, chronic HSDN C4084774 Have weight loss C0002940 Aneurysm HSDN C3887873 Hearing loss C0011853 Diabetes mellitus, experimental HSDN C4084767 Bothered by vomiting C3495422 Finding relating to sexuality and sexual activity HSDN C2237041 Shox gene with short stature C3150607 Chromosome 17q23.1-q23.2 deletion syndrome MalaCards C0242936 Center pain C0019202 Hepatolenticular degeneration HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0042338 Herpesvirus 3, human HSDN C0018681 Headache, cephalalgia C0036946 Sheep--diseases HSDN C0036572 Convulsion C0241158 Cicatrix skin HSDN C4084775 Usual severity weight loss C0042995 Vulvar neoplasms HSDN C0010038 Corneal opacity disorder C0028860 Oculocerebrorenal syndrome HPO C0017672 Pain tongue C1999266 Depression adverse event HSDN C0015672 Decreased energy C0033953 Psychosexual disorders HSDN C0027497 Queasy C0022758 Kap HSDN C3887873 Hearing loss C0006663 Calcinosis HSDN C0030232 Color loss C3808920 Anemia, hypochromic microcytic, with iron overload 2 MalaCards C2032395 Pelvic pain on the left C3244301 Coverage level - family HSDN C3829611 Nausea frequency C0151740 Intracranial hypertension HSDN C0011991 Loose stools C2931242 Familial waldmann's disease MalaCards C4084767 Bothered by vomiting C0007766 Intracranial aneurysm HSDN C3641756 Have diarrhea C0041234 Chagas disease OrphaNet|MalaCards C0015300 Ocular proptosis C1866182 Penttinen-aula syndrome MalaCards|HPO C0043094 Weight gain C0042830 Perception visual HSDN C0023014 Developmental disorder language C2720434 Macroencephaly HSDN C3539890 Pelvic pain causes awakening at night C2936403 46, xx disorders of sex development HSDN C1549543 Administration method - pain C0022729 Klebsiella infections HSDN C0042024 Urine incontinence C0340629 Aortic aneurysm without mention of rupture nos HSDN C1963170 Hypothermia adverse event C0011849 Diabetes mellitus HSDN C1384666 Decreased hearing C0406556 Hereditary acrokeratotic poikiloderma of weary MalaCards|HPO C2919142 Short stature adverse event C0017205 Gaucher disease MalaCards C1963180 Neck pain adverse event C0019080 Hemorrhage HSDN C4085210 Usual severity pain C0004782 Basal ganglia diseases HSDN C1384666 Decreased hearing C0021368 Inflammation HSDN C0019079 Bloody sputum C0028242 Nocardia infections HSDN C0039070 Collapse fleeting C0022660 Kidney failure, acute HSDN|UMLS C3274924 Have been coughing C0032131 Plasmacytoma HSDN C4085211 Pain distress question C0026528 Moral code HSDN C0015469 Facial paralysis C0014121 Bacterial endocarditis HSDN C1962972 Proteinuria adverse event C1851986 Dyschondrosteosis and nephritis OrphaNet|MalaCards C0151740 Intracranial hypertension C1848814 Thymoma, familial MalaCards C0024031 Back pain lower back C2911243 Encounter due to family history of colonic polyps HSDN C2984058 Have pain C1532253 Sedentary lifestyle HSDN C4085222 Nausea C0023055 Laryngeal neoplasm HSDN C0018772 Deafness C2931452 Hirschsprung disease, deafness and polydactyly MalaCards C1963091 Diarrhea adverse event C0242339 Dyslipidemias HSDN C2984058 Have pain C0023761 Lip neoplasms HSDN C0018772 Deafness C0007761 Myoclonic cerebellar dyssynergia HSDN C0018681 Headache, cephalalgia C3897755 Recurrent childhood fibrillary astrocytoma UMLS C4085317 Diarrhea frequency C1739094 Foodborne botulism OrphaNet|MalaCards C4084784 Diarrhea C0014571 Epiphyses, slipped HSDN C3539896 Pelvic pain occurs with urination C0009244 Behavioral cognitive therapy HSDN C0000737 Abdomen pain C1336263 Ovarian yolk sac tumor stage iii UMLS C0011570 Monopolar depression C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C0030975 Disorders perception C0001175 Acquired immunodeficiency syndrome HSDN C0004134 Dyssynergia C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards|HPO|UMLS C1549543 Administration method - pain C0042162 Uveal neoplasms HSDN C0027796 Neuralgias C1963119 Stomach ulcer adverse event HSDN C0027497 Queasy C0004610 Bacteremia HSDN C0013456 Pain ear C0027438 Nasopharynx HSDN C1549543 Administration method - pain C0017671 Glomus jugulare tumor HSDN C0022346 Yellow skin C0018799 Heart diseases HSDN C4084768 Usual severity vomiting C0268568 Classic maple syrup urine disease HPO C4084724 Usual severity constipation C0022758 Kap HSDN C0020903 Illusion C0030477 Personality disorder paranoid HSDN C3641755 Have constipation C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C0042963 Symptoms vomiting C0262584 Carcinoma, small cell HSDN C0349588 Stature short C0268225 Aspartylglucosaminuria MalaCards|HPO C2096293 Ent surgical result ear vertigo C0079731 B-cell lymphomas HSDN C0235153 Sensory hallucination C0268569 Intermittent maple syrup urine disease HPO C3641756 Have diarrhea C1333419 Epithelial hepatic and intrahepatic bile duct neoplasm MalaCards C0043094 Weight gain C0085129 Bronchial hyperreactivity HSDN C3641755 Have constipation C0348018 Projections HSDN C4084769 Vomiting frequency C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0041834 Erythematous condition C0021368 Inflammation MalaCards C4084767 Bothered by vomiting C1855652 Fetus small for gestational age HSDN C4085210 Usual severity pain C0027658 Neoplasms, germ cell and embryonal HSDN C3463815 Feel fatigue C0026771 Trauma multiple HSDN C2919142 Short stature adverse event C1833691 Otofaciocervical syndrome OrphaNet|HPO C3898969 Have been vomiting C0205710 Alpers syndrome (disorder) MalaCards|HPO C0015672 Decreased energy C0281479 Primary systemic amyloidosis MalaCards C0026205 Pupillary constriction C0017612 Glaucoma, open-angle HSDN C0036572 Convulsion C1333283 Diaphragm sellae meningioma UMLS C0007398 Catatonic C0036356 Schizophrenics--language HSDN C3829611 Nausea frequency C0700095 Central neuroblastoma HSDN C2984057 Have nausea C0027819 Neuroblastoma HSDN C0030552 Paralysis partial C0023176 Lead poisoning MalaCards C4084773 Bothered by weight gain C0020473 Hyperlipidemia HSDN C0518090 Frequency of pain question C0013922 Embolism HSDN C0010200 Cough symptom C0020523 Immediate hypersensitivity HSDN C1549543 Administration method - pain C0010038 Corneal opacity HSDN C0032617 High urine output C0043207 Wolfram syndrome HSDN C0234376 Tremor action C1834712 Cerebellar granule cell hypertrophy and megalencephaly HPO C0233765 Hallucination olfactory C0018524 Hallucinations UMLS C1963093 Dizziness adverse event C1636667 Disorder characterized by eosinophilia HSDN C4084774 Have weight loss C0034628 Radius fracture HSDN C0042571 Vertigo subjective C0460137 Push down or depress HSDN C0917816 Deficiency mental C0268080 Hypercalcemia, idiopathic, of infancy HPO C1579931 Depressed - symptom C3150344 Hyperhomocysteinemia, thrombotic, cbs-related HPO C2984057 Have nausea C1145670 Respiratory failure HSDN C4085317 Diarrhea frequency C0020627 Hypopharyngeal neoplasms HSDN C0150055 Pain chronic C0020538 Hypertensive disease HSDN C1838869 Proximal neurogenic muscle weakness C3810285 Myopathy with extrapyramidal signs MalaCards C0018772 Deafness C0751871 Autoimmune diseases of the nervous system HSDN C0013404 Respiratory difficulty C0042514 Tachycardia, ventricular HSDN C0013604 Edematous C0349622 Hemangiopericytoma of meninges HSDN C0036572 Convulsion C0031090 Periodontal diseases HSDN C0221166 Paraparesis C0349606 Central nervous system cysts HSDN C4085549 Dizziness C0751815 Carotid artery, internal, dissection HSDN C0039070 Collapse fleeting C0004153 Atherosclerosis HSDN C4084774 Have weight loss C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0020673 Hypothermia (central) (local) C4053506 Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation MalaCards C0023015 Language handicap C0041409 Turner syndrome, male HSDN C0042963 Symptoms vomiting C0233757 Psychogenic vomiting nos UMLS C4085548 Usual severity dizziness C0041327 Tuberculosis, pulmonary HSDN C0036572 Convulsion C1962971 Myocarditis adverse event HSDN C0031911 Pigment deposition C0346037 Acral lentiginous malignant melanoma MalaCards C0008031 Pain chest C1540912 Hypereosinophilic syndrome HSDN C0019209 Large liver C0221032 Familial generalized lipodystrophy OrphaNet|HPO|MalaCards C4085211 Pain distress question C0037417 Identification, social HSDN C0015672 Decreased energy C0043253 Trauma blunt HSDN C2984058 Have pain C0041351 Tularemia HSDN C0234146 Absent reflex C2750090 Charcot-marie-tooth disease, axonal, type 2n MalaCards|HPO C0003811 Cardiac rhythm disturbance C1832600 Naxos disease OrphaNet|MalaCards C2237041 Shox gene with short stature C1856871 Aarskog-like syndrome OrphaNet|MalaCards C1971624 Appetite absent C0854795 Resectable hepatic malignant neoplasm MalaCards C0427190 Ataxia, truncal C0406586 Congenital pseudohydrocephalic progeroid syndrome MalaCards|UMLS C3539023 Pelvic pain increasing in frequency C0037856 Spermatic cord torsion HSDN C2984058 Have pain C0004763 Barrett esophagus HSDN C0000737 Abdomen pain C1335686 Neuroendocrine neoplasm of rectum MalaCards C0151786 Weakness muscle C1706192 Sulfatidosis MalaCards C4084776 Weight loss C0006277 Bronchitis HSDN C4084784 Diarrhea C2751492 Amyloidosis, hereditary, transthyretin-related MalaCards|HPO C0917816 Deficiency mental C1860789 Leukemia, megakaryoblastic, of down syndrome HPO C2024893 Cardiovascular surgery result: fatigue C0872996 Q fever vaccine HSDN C4084723 Constipation C0006264 Bronchial neoplasms HSDN C0019209 Large liver C0376300 Dengue shock syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C1762616 Meningioma, benign, no icd-o subtype HSDN C3541349 Syncope C2984291 Glioblastoma multiforme pathway HSDN C0004134 Dyssynergia C0338443 Acute cerebellar ataxia caused by varicella UMLS C0018681 Headache, cephalalgia C0024266 Lymphocytic choriomeningitis DiseaseOntology|MalaCards C0007758 Cerebellar ataxia C0037397 Behavior social HSDN C0557874 Global developmental delay C0265328 Alopecia-epilepsy-oligophrenia syndrome MalaCards C2024878 Cardiovascular surgery result: dyspnea C0027651 Tumor HSDN C1557397 Adverse event associated with pain C0033054 Prenatal exposure delayed effects HSDN C3539896 Pelvic pain occurs with urination C0012746 Dissociative disorder HSDN C0000737 Abdomen pain C0004626 Pneumonia, bacterial HSDN C1963184 Nystagmus adverse event C3150191 Coloboma, ocular, and ichthyosis, brain malformations, and endocrine abnormalities MalaCards|HPO C0042963 Symptoms vomiting C0920350 Autoimmune thyroiditis HSDN C4084802 Usual severity diarrhea C0001618 Tumors of adrenal cortex HSDN C0018772 Deafness C0795910 Cowchock syndrome OrphaNet|HPO|MalaCards C3539892 Pelvic pain in front C1394494 Cystocele, unspecified HSDN C0241137 Skin pallor C3279664 Emberger syndrome MalaCards C0009676 Confusion state C0007222 Cardiovascular diseases HSDN C0004604 Pain back C0031214 Measure personality HSDN C0578056 Pain of truncal structure C0457949 Chronic low back pain UMLS C4084769 Vomiting frequency C0162871 Aortic aneurysm, abdominal HSDN C2984057 Have nausea C0014121 Bacterial endocarditis HSDN C1321898 Bloody stool C2243088 Idiopathic erosive/hemorrhagic gastritis UMLS C2919142 Short stature adverse event C3151433 Osteogenesis imperfecta, type xii MalaCards C0030193 Sense of pain C0033999 Pterygium HSDN C4085548 Usual severity dizziness C0024115 Lung diseases HSDN C0848203 Male pelvic pain C0020550 Hyperthyroidism HSDN C0036659 Sensation disorder C0796561 Melanoma vaccines HSDN C4085210 Usual severity pain C0206180 Ki-1+ anaplastic large cell lymphoma HSDN C2029884 Hearing loss by exam C0014761 Erythroblastosis, fetal HSDN C0424755 Fever symptoms C0034734 Raynaud disease HSDN C4085211 Pain distress question C0007762 Cerebellar neoplasms HSDN C1549543 Administration method - pain C0013504 Echinococcosis, hepatic HSDN C2919142 Short stature adverse event C2713347 7-dehydrocholesterol reductase deficiency OrphaNet|MalaCards C2919142 Short stature adverse event C0752166 Bardet-biedl syndrome OrphaNet|HPO|MalaCards C3641756 Have diarrhea C0023267 Fibroid tumor HSDN C4084802 Usual severity diarrhea C0149778 Soft tissue infections HSDN C0018784 Deafness sensorineural C0040715 Chromosomal translocation HSDN C0013421 Dystonia C0011303 Demyelinating diseases HSDN C1963184 Nystagmus adverse event C1854369 Spinocerebellar ataxia 14 MalaCards|HPO C4084766 Vomiting C0021228 Variability of individual responses HSDN C0011175 Deficient fluid volume C1533628 Pseudo-zellweger syndrome MalaCards C3203358 Alveolar hypoventilation C2986717 Anti-n-methyl-d-aspartate receptor encephalitis HSDN C1963087 Constipation adverse event C0032371 Poliomyelitis HSDN C1145670 Failure respiratory C2930815 Acute cerebral gaucher disease MalaCards C0042963 Symptoms vomiting C0752140 Intracranial embolism HSDN C1963091 Diarrhea adverse event C0037661 Somatostatinoma OrphaNet|MalaCards C0021359 Infertility C3151343 Spinocerebellar ataxia 32 MalaCards C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C3641755 Have constipation C0221069 Anterior spinal artery syndrome HSDN C0040822 D tremors C0175702 Williams syndrome OrphaNet|HPO|MalaCards C4084725 Usual severity cough C0042133 Uterine fibroids HSDN C2984058 Have pain C0282507 Heat stress disorders HSDN C4084775 Usual severity weight loss C1956391 Temporal arteritis OrphaNet|HPO|MalaCards C0030193 Sense of pain C0347894 Neuralgia, neuritis and radiculitis unspecified UMLS C0413252 Hypothermia due to exposure C0022744 Knee injury HSDN C0013428 Painful urination C0810038 Genitourinary symptoms and ill-defined conditions UMLS C0022346 Yellow skin C0400979 Obstruction of biliary tree UMLS C1963281 Vomiting adverse event C0032269 Pneumococcal infections HSDN C0007758 Cerebellar ataxia C0019202 Hepatolenticular degeneration HSDN C0423610 Female genital pain C0013394 Coitus painful UMLS C0040460 Dental pain C0037286 Skin neoplasms HSDN C0427055 Face weakness C0432273 Worth disease HPO C4084767 Bothered by vomiting C0039730 Thalassemia HSDN C0028738 Nystagmus C0338488 Alternating hemiplegia of childhood HPO C0038990 Sweats C0017547 Gigantism OrphaNet C0020305 Fetal edema C1849554 Lymphangiectasia, pulmonary, congenital OrphaNet|MalaCards C0917801 Sleep disorder insomnia C0154566 Transient disorder of initiating or maintaining sleep UMLS C0040485 Wryneck C3888031 Spinocerebellar ataxia 35 MalaCards C2024893 Cardiovascular surgery result: fatigue C0040456 Tooth impaction HSDN C2242996 Tingling C0752191 Central nervous system schistosomiasis HSDN C0010200 Cough symptom C2936664 Acquired hypogammaglobulinemia HSDN C0003469 Anxiety disorder C0020428 Hyperaldosteronism MalaCards C0020505 Excessive eating C0949628 Uniparental disomy HSDN C0000737 Abdomen pain C1297884 Musculo-aponeurotic fibromatosis MalaCards C3641755 Have constipation C3203358 Hypoventilation MalaCards C0007859 Pain neck C0042373 Vascular diseases HSDN C0018772 Deafness C0017636 Glioblastoma HSDN C0018681 Headache, cephalalgia C0276180 Monkey pox MalaCards C0026884 Muteness C0007786 Brain ischemia HSDN C1279888 Proteinuria of undiagnosed cause C1963229 Retinal detachment adverse event HSDN C1963091 Diarrhea adverse event C3150207 Agammaglobulinemia 6, autosomal recessive HPO C2237041 Shox gene with short stature C0175694 Smith-lemli-opitz syndrome OrphaNet|HPO|MalaCards C4085211 Pain distress question C0009953 Convulsive therapy HSDN C2188457 Urinary incontinence without sensory awareness of fullness C0042024 Urinary incontinence UMLS C1557397 Adverse event associated with pain C3244301 Coverage level - family HSDN C1963071 Back pain adverse event C0004933 Behavior modification technique HSDN C1549543 Administration method - pain C0025290 Aseptic meningitis HSDN C0007166 Cardiac output decreased C1963198 Pancreatitis adverse event HSDN C0151786 Weakness muscle C0677607 Hashimoto disease HSDN C0151786 Weakness muscle C1263858 Muscular dystrophy congenital, merosin negative OrphaNet C2919142 Short stature adverse event C0175693 Russell-silver syndrome OrphaNet|MalaCards C0277959 Hair coarseness C0263491 Pili torti MalaCards C1963087 Constipation adverse event C0206718 Ganglioneuroblastoma HSDN C0018777 Deafness, conductive C0265232 Frontonasal dysplasia anomalad MalaCards C2984058 Have pain C0025281 Meniere disease HSDN C3898969 Have been vomiting C0036946 Sheep--diseases HSDN C0007758 Cerebellar ataxia C1847501 Glut1 deficiency syndrome OrphaNet|MalaCards C0948628 Haemorrhoid bleeding friction rub C0265031 Hemorrhoid bleeding UMLS C1557397 Adverse event associated with pain C0010606 Adenoid cystic carcinoma HSDN C0242936 Center pain C0019357 Keratitis, herpetic HSDN C0013404 Respiratory difficulty C0020473 Hyperlipidemia HSDN C3274924 Have been coughing C0006118 Brain neoplasms HSDN C1962972 Proteinuria adverse event C0079487 Helicobacter infections HSDN C0030554 Abnormal sensation C3494506 Pseudohypoparathyroidism, type ia HPO C0009792 Consciousness disorder C0270639 Lateral sinus thrombosis HSDN C0018772 Deafness C0079584 Ichthyosis vulgaris HSDN C0042963 Symptoms vomiting C0346303 Thyrotroph adenoma OrphaNet|MalaCards C1963066 Joint pain adverse event C0030636 Pasteurella infection DiseaseOntology C1963087 Constipation adverse event C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0231712 Gait waddling C1836050 Filaminopathy, autosomal dominant MalaCards|HPO|UMLS C4084776 Weight loss C0242707 Ventricular dysfunction, right HSDN C0019209 Large liver C0751038 Cockayne syndrome, type ii HPO C0522224 Palsied C0027902 Neuropsychological diagnosis HSDN C3541349 Syncope C0016045 Fibroma HSDN C4084723 Constipation C0795623 Hepatitis a vaccine, inactivated HSDN C1963170 Hypothermia adverse event C1963137 Hydrocephalus adverse event HSDN C0037763 Spasm C0039978 Thoracic diseases HSDN C0018784 Deafness sensorineural C1847089 Usher syndrome, type ig HPO C4084802 Usual severity diarrhea C0019655 Histoplasmosis HSDN C0242936 Center pain C1691228 Cystic kidney diseases HSDN C4084776 Weight loss C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0856078 Enuresis aggravated C0014394 Enuresis UMLS C0024031 Back pain lower back C2014415 Orthopedic disorder of spine UMLS C1384666 Decreased hearing C3554519 Cowden syndrome 6 MalaCards C2315100 Pediatric failure to thrive C1969038 Renal tubular acidosis, distal, with hemolytic anemia (disorder) HPO C0030193 Sense of pain C0036130 Salpingitis HSDN C4084768 Usual severity vomiting C0012739 Disseminated intravascular coagulation HSDN C2919142 Short stature adverse event C0268556 Saccharopinuria MalaCards|HPO C2055125 Temperature reported over 102 degrees fahrenheit C0014060 Encephalitis, st. louis DiseaseOntology|MalaCards C3887873 Hearing loss C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0035232 Diaphragmatic paralysis C0027531 Neck injury HSDN C4084784 Diarrhea C0030922 Peptic ulcer hemorrhage HSDN C0003910 Articulation disorder C0004936 Mental disorders HSDN C1279888 Proteinuria of undiagnosed cause C0023890 Liver cirrhosis HSDN C0004134 Dyssynergia C0010964 Dandy-walker syndrome HSDN C0040822 D tremors C0796561 Melanoma vaccines HSDN C0024031 Back pain lower back C0206734 Hemangioblastoma HSDN C0574002 Foot swelling C0878544 Cardiomyopathies UMLS C0003126 Smell loss C1833473 Dermoid cysts, familial frontonasal MalaCards C4084768 Usual severity vomiting C2931876 Hirschsprung disease 1 MalaCards C0018784 Deafness sensorineural C0033300 Progeria OrphaNet|HPO C0151827 Pain eye C0005741 Blepharitis HSDN C4084766 Vomiting C0019537 High pressure nervous syndrome HSDN C0036572 Convulsion C0028758 Bonding HSDN C4085222 Nausea C2945560 Hemolytic HSDN C4085642 Level of joint stiffness C1859721 Arthrogryposis multiplex congenita, neurogenic type (disorder) OrphaNet|MalaCards C0030193 Sense of pain C0007121 Bronchogenic carcinoma HSDN C3829611 Nausea frequency C1548578 Location characteristic id - smoking HSDN C0042798 Vision dim C0796085 Nance-horan syndrome OrphaNet|HPO|MalaCards C0233773 Hallucinations hypnogogic C1836907 Narcolepsy 3 MalaCards|UMLS C4085210 Usual severity pain C0025061 Disease of mediastinum HSDN C0001825 Agraphia C0007774 Cerebral arterial diseases HSDN C4084802 Usual severity diarrhea C0026850 Muscular dystrophy HSDN C0042798 Vision dim C0796021 Lowry wood syndrome MalaCards C4085222 Nausea C0007137 Squamous cell carcinoma HSDN C0002965 Crescendo angina C0037313 Sleep HSDN C0413252 Hypothermia due to exposure C0085096 Peripheral vascular diseases HSDN C1961131 Cough adverse event C0032226 Pleural diseases HSDN C4084774 Have weight loss C1522133 High cholesterol level HSDN C1961131 Cough adverse event C0019337 Heroin dependence HSDN C1384666 Decreased hearing C0026946 Mycoses HSDN C0013404 Respiratory difficulty C0025286 Meningioma HSDN C0428977 Pulse rate decrease C1833661 Paroxysmal extreme pain disorder MalaCards|HPO C0018926 Emesis bloody C0008626 Congenital chromosomal disease HSDN C0039070 Collapse fleeting C4049644 Depression HSDN C0039231 Heartbeats increased C1843687 Atrial fibrillation, familial, 1 (disorder) MalaCards C1557397 Adverse event associated with pain C0036879 Education sex HSDN C4084726 Distress cough C0018200 Granuloma, respiratory tract HSDN C0001825 Agraphia C2137063 Ent surgical result - speech HSDN C0162292 Extraocular palsy C0410203 X-linked centronuclear myopathy OrphaNet|HPO C2203646 Jaundice C1334928 Necrotic changes (finding) HSDN C1963281 Vomiting adverse event C0027092 Myopia HSDN C0036572 Convulsion C0750394 Wbc low HSDN C4084726 Distress cough C0011853 Diabetes mellitus, experimental HSDN C0027796 Neuralgias C0007786 Brain ischemia HSDN C4084897 Sleep disturbance subordinate domain C3502510 Chromosome 16p13.3 deletion syndrome MalaCards C0413252 Hypothermia due to exposure C0000771 Abnormalities, drug induced HSDN C4084766 Vomiting C1963266 Uveitis adverse event HSDN C3463815 Feel fatigue C0010606 Adenoid cystic carcinoma HSDN C4084774 Have weight loss C0011993 Vipoma OrphaNet|MalaCards C0542218 Sore roof of mouth C0038362 Stomatitis UMLS C4084792 Usual severity hair loss C1148551 X-linked dyskeratosis congenita MalaCards C4084773 Bothered by weight gain C0024115 Lung diseases HSDN C2984058 Have pain C0003723 Arbovirus infections HSDN C0151786 Weakness muscle C0006277 Bronchitis HSDN C1963091 Diarrhea adverse event C0038220 Status epilepticus HSDN C0853986 Lymphocytes decreased C1876175 Ataxia-telangiectasia variant MalaCards C4042891 Sleep wake disorders C0006261 Bronchial diseases HSDN C4085317 Diarrhea frequency C0007177 Cardiac tamponade HSDN C4084769 Vomiting frequency C0033975 Psychotic disorders HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0015927 Intrauterine fetal demise HSDN C0018775 Hearing loss bilateral C0717360 Disease lyme vaccine HSDN C0349588 Stature short C3697628 Biason-lauber syndrome MalaCards C4049644 Depression C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C0151786 Weakness muscle C3536984 Vitamin d-resistant rickets, x-linked HSDN C1963086 Confusion adverse event C1832903 Migraine, sporadic hemiplegic HPO C0007758 Cerebellar ataxia C0919267 Ovarian neoplasm HSDN C0026821 Cramp C0005967 Bone neoplasms HSDN C0018772 Deafness C0042870 Vitamin d deficiency HSDN C0231791 In toe C0342282 Symphalangism-brachydactyly syndrome OrphaNet C0349489 Fetal hypoxia C0003886 Arthrogryposis HSDN C0040034 Thrombocytopenia C0392475 Roberts-sc phocomelia syndrome MalaCards|HPO C2242996 Tingling C0023804 Lipomatosis, multiple symmetrical OrphaNet|HPO|MalaCards C0042420 Vasovagal episode C1962958 Hematoma adverse event HSDN C4084802 Usual severity diarrhea C0242350 Erectile dysfunction HSDN C2024878 Cardiovascular surgery result: dyspnea C2984291 Glioblastoma multiforme pathway HSDN C4084766 Vomiting C0342873 Glutaric aciduria iii MalaCards|HPO C0221263 Cafe au lait spot C0018564 Hand deformities HSDN C4085642 Level of joint stiffness C1855772 Absent corpus callosum cataract immunodeficiency MalaCards|HPO C1962957 Flushing adverse event C0030318 Panic state HSDN C0026821 Cramp C0497327 Dementia HSDN C0015230 Exanthem C0043195 Subsepsis hyperergia syndrome OrphaNet|MalaCards C0028081 Night sweat C0153767 Hodgkin's nod.scl.-multip.site UMLS C0042384 Vasculitis, nonspecific C0001733 Afibrinogenemia HPO C0030554 Abnormal sensation C0024445 Lipomatosis, familial benign cervical OrphaNet|HPO|MalaCards C0042928 Paralysis vocal cord C1145628 Autonomic nervous system disorders HSDN C0002962 Angina C1145628 Autonomic nervous system disorders HSDN C4084725 Usual severity cough C0036329 Schistosomiasis japonica DiseaseOntology C3146279 Coma C0001403 Addison disease HSDN C0042571 Vertigo subjective C0020542 Pulmonary hypertension HSDN C0042510 Fibrillation paroxysmal vent C2751898 Ventricular fibrillation, paroxysmal familial, 1 HPO C2919142 Short stature adverse event C0265421 Warkany syndrome MalaCards C0009806 Constipate C0025162 Megacolon toxic HSDN C0030193 Sense of pain C0029422 Osteochondrodysplasias HSDN C3829611 Nausea frequency C0016057 Fibrosarcoma HSDN C0426579 Anorexia symptom C2931842 Diaphyseal dysplasia 1, progressive MalaCards C0003469 Anxiety disorder C0036391 Schwartz-jampel syndrome MalaCards|HPO C0030486 Extremity paralysis, lower C0017185 Gastrointestinal neoplasms HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0018924 Hemarthrosis HSDN C4084802 Usual severity diarrhea C0854795 Resectable hepatic malignant neoplasm MalaCards C0009421 Comatose C0151744 Myocardial ischemia HSDN C1549543 Administration method - pain C0006437 Burn, inhalation HSDN C0522224 Palsied C0162872 Aortic aneurysm, thoracic HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0010709 Cyst HSDN C0018772 Deafness C0018946 Hematoma, subdural HSDN C1557397 Adverse event associated with pain C0034884 Rectal fistula HSDN C4085210 Usual severity pain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C1971624 Appetite absent C1546533 Specimen source codes - abscess HSDN C1557397 Adverse event associated with pain C0242788 Breast neoplasms, male HSDN C3203358 Alveolar hypoventilation C0011581 Depressive disorder HSDN C0037316 Not enough sleeping C0795623 Hepatitis a vaccine, inactivated HSDN C0851578 Disorder sleep C1412278 Ager gene HSDN C0034124 Pupillary disorder C0043255 Stab wound HSDN C4084776 Weight loss C0010246 Coxsackievirus infections HSDN C3829611 Nausea frequency C1423541 Vangl2 gene HSDN C0037384 Snore C1552262 Nurse practitioner - family HSDN C0000737 Abdomen pain C0034040 Puerperal disorders HSDN C0011991 Loose stools C0016510 Foot diseases HSDN C4084725 Usual severity cough C2117118 X-ray of toe: deformity contracture HSDN C2911645 Weight loss adverse event C1853564 Developmental delay, epilepsy, and neonatal diabetes MalaCards C0019825 Voice hoarseness C0005491 Biofeedback HSDN C4084766 Vomiting C0524851 Neurodegenerative disorders HSDN C1963180 Neck pain adverse event C0001418 Adenocarcinoma HSDN C0030794 Pelvis pain C0019553 Contracture hips HSDN C0020673 Hypothermia (central) (local) C0015695 Fatty liver HSDN C0018772 Deafness C0008441 Chondroblastoma HSDN C0030486 Extremity paralysis, lower C0035435 Rheumatism HSDN C2029884 Hearing loss by exam C0033817 Pseudomonas infections HSDN C4085548 Usual severity dizziness C0015663 Fasting HSDN C0151686 Growth retardation C0795956 Chylomicron retention disease OrphaNet|HPO|MalaCards C0152227 Tearing excessive C0600176 Argentaffinoma MalaCards C2984058 Have pain C1384607 Food deprivation HSDN C0030552 Paralysis partial C0032851 Disease poultry HSDN C0033774 Skin pruritus C1704272 Benign prostatic hyperplasia HSDN C0015672 Decreased energy C0343771 Human ehrlichiosis MalaCards C0151786 Weakness muscle C0544012 Aberfeld's syndrome MalaCards C0019209 Large liver C1856245 Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type ii HPO C1527344 Dysphonia C0270952 Muscular dystrophy, oculopharyngeal HSDN C2984058 Have pain C0027726 Nephrotic syndrome HSDN C0848203 Male pelvic pain C0520720 Cyst nerve root HSDN C4085222 Nausea C0460137 Push down or depress HSDN C0040485 Wryneck C2911643 Encounter due to family history of osteoporosis HSDN C1963091 Diarrhea adverse event C0043515 Zollinger-ellison syndrome OrphaNet|MalaCards C0004134 Dyssynergia C0002534 Renal aminoacidurias HSDN C1963252 Tremor adverse event C0024305 Lymphoma, non-hodgkin HSDN C4084767 Bothered by vomiting C1283620 Sucrase-isomaltase deficiency, congenital OrphaNet|MalaCards C4084773 Bothered by weight gain C0000786 Spontaneous abortion HSDN C0026838 Spasticity muscle C0021368 Inflammation HSDN C0009421 Comatose C0027531 Neck injury HSDN C0042963 Symptoms vomiting C0012739 Disseminated intravascular coagulation HSDN C4084726 Distress cough C0038463 Strongyloides infection HSDN C0009763 Conjunctiva inflammation C1275126 Tnf receptor-associated periodic fever syndrome (traps) HPO C4084766 Vomiting C0015927 Intrauterine fetal demise HSDN C0853986 Lymphocytes decreased C0085110 Severe combined immunodeficiency OrphaNet|MalaCards C1557397 Adverse event associated with pain C0003466 Anus, imperforate HSDN C0015300 Ocular proptosis C1838329 Aplasia cutis congenita with epibulbar dermoids MalaCards C1549543 Administration method - pain C0235146 Emotionally high HSDN C0002962 Angina C0032914 Pre-eclampsia HSDN C0002962 Angina C0812393 Cancer patients and suicide and depression HSDN C0011991 Loose stools C0276468 Epidemic diarrheal disease of infant mouse UMLS C0043094 Weight gain C0029928 Ovarian diseases HSDN C0042940 Disorder of voice C0037942 Spinal osteophytosis HSDN C0040034 Thrombocytopenia C1832388 Platelet disorder, familial, with associated myeloid malignancy MalaCards|HPO C4084776 Weight loss C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C0042798 Vision dim C0002875 Cooley's anemia HPO C0005745 Blepharoptosis C1970107 Ataxia, spastic, 1, autosomal dominant MalaCards|HPO C0033774 Skin pruritus C0018802 Congestive heart failure HSDN C0242936 Center pain C0266015 Congenital digestive system anomalies HSDN C1549543 Administration method - pain C0014457 Eosinophilia HSDN C4084774 Have weight loss C0020676 Hypothyroidism HSDN C4085549 Dizziness C0243026 Sepsis HSDN C0018991 Paralysis one side of body C0011265 Presenile dementia HSDN C1279888 Proteinuria of undiagnosed cause C0265345 Lymphedema distichiasis syndrome MalaCards|HPO C0038002 Spleen enlargement C2713321 Alpha-l-iduronidase deficiency OrphaNet C4084766 Vomiting C0008350 Cholelithiasis HSDN C4084774 Have weight loss C0030305 Pancreatitis HSDN C1549543 Administration method - pain C0021308 Infarction HSDN C0019209 Large liver C3888018 Congenital hyperinsulinism MalaCards C2984058 Have pain C0497573 Condylomata acuminata in women HSDN C1963071 Back pain adverse event C0011603 Dermatitis HSDN C4084788 Have dizziness C0012644 Animal disease models HSDN C0036572 Convulsion C1863727 Hemophagocytic lymphohistiocytosis, familial, 2 MalaCards|HPO|UMLS C0341866 Menopausal sleeplessness C0404559 Perimenopausal disorder UMLS C4084725 Usual severity cough C0011603 Dermatitis HSDN C0007758 Cerebellar ataxia C0850803 Anaphylaxis (non medication) HSDN C0242936 Center pain C0034362 Q fever HSDN C4085317 Diarrhea frequency C0024810 Marijuana smoking HSDN C0018991 Paralysis one side of body C0002992 Angiomatosis HSDN C0234146 Absent reflex C0410204 Myopathy, centronuclear, autosomal recessive HPO C0004604 Pain back C0013295 Duodenal ulcer HSDN C0030200 Intractable pain C0021603 Sleep initiation and maintenance disorders HSDN C0027497 Queasy C0001624 Adrenal gland neoplasms HSDN C3274924 Have been coughing C0021361 Female infertility HSDN C1963091 Diarrhea adverse event C0011848 Diabetes insipidus HSDN C4085211 Pain distress question C0025521 Inborn errors of metabolism HSDN C0008031 Pain chest C1709884 Regional adrenal gland chromaffin neoplasm UMLS C1961131 Cough adverse event C0270611 Brain damage HSDN C0013421 Dystonia C2984291 Glioblastoma multiforme pathway HSDN C4084775 Usual severity weight loss C0016662 Fracture open HSDN C0005745 Blepharoptosis C0220658 Pfeiffer syndrome OrphaNet|MalaCards C1963091 Diarrhea adverse event C0023223 Leg ulcer HSDN C0237326 Defecation pain C1882278 Interacinar cell pancreatic polypeptide tumor MalaCards C0026826 High muscle tone C1855368 Maple syrup urine disease, e3 deficient, with lactic acidosis HPO C4084774 Have weight loss C0009326 Collagen diseases HSDN C0000737 Abdomen pain C0269886 Inversion of uterus HSDN C0013362 Dysarthrias C0023241 Legionnaires' disease HSDN C0018772 Deafness C0025149 Medulloblastoma HSDN C0035078 Failure kidney C0043398 Yellow fever, urban MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C3539893 Pelvic pain occurs with intercourse C0007527 Cecal disease HSDN C0004134 Dyssynergia C0039223 Tabes dorsalis UMLS C0036572 Convulsion C1855371 Maple syrup urine disease, type ii HPO C4049644 Depression C0012236 Digeorge syndrome MalaCards C3829611 Nausea frequency C2711591 Infection by anisakidae MalaCards C1962957 Flushing adverse event C0031511 Pheochromocytoma MalaCards|HSDN C1962972 Proteinuria adverse event C0040100 Thymoma HSDN C0000737 Abdomen pain C0041327 Tuberculosis, pulmonary HSDN C4084726 Distress cough C0600467 Neurogenic inflammation HSDN C0018965 Blood urine C1567741 Alport syndrome OrphaNet C0024031 Back pain lower back C0039538 Teratoma HSDN C0010200 Cough symptom C0702166 Acne HSDN C3541349 Syncope C0162820 Dermatitis, allergic contact HSDN C4085210 Usual severity pain C0023976 Long qt syndrome HSDN C4084775 Usual severity weight loss C0263666 Dermatomyositis, childhood type MalaCards C2029884 Hearing loss by exam C0029464 Osteosclerosis HSDN C0413252 Hypothermia due to exposure C0006840 Candidiasis HSDN C0015799 Feminisation C0001430 Adenoma HSDN C4084775 Usual severity weight loss C0524909 Hepatitis b, chronic HSDN C2237041 Shox gene with short stature C0796066 Microcephaly-cervical spine fusion anomalies OrphaNet|MalaCards C2315100 Pediatric failure to thrive C1844696 Otopalatodigital syndrome, type ii OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0023473 Myeloid leukemia, chronic HSDN C1557397 Adverse event associated with pain C0282607 Vascular neoplasms HSDN C0018772 Deafness C0006309 Brucellosis HSDN C4084723 Constipation C0242647 Mucosa-associated lymphoid tissue lymphoma OrphaNet|HPO C0237326 Defecation pain C1833661 Paroxysmal extreme pain disorder OrphaNet|HPO|MalaCards C0151786 Weakness muscle C0006035 Borrelia infections MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0085682 Hypophosphatemia HSDN C0151889 Reflexes tendon increased C1851920 Dopa-responsive dystonia HPO C3887873 Hearing loss C0919267 Ovarian neoplasm HSDN C0012833 Dizzy C2364172 Adherence to medication regime HSDN C4085549 Dizziness C0003811 Cardiac arrhythmia HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023443 Hairy cell leukemia HSDN C4085549 Dizziness C0003507 Aortic valve stenosis HSDN C0016382 Cutaneous vascular engorgement C0206728 Plexiform neurofibroma HSDN C3714552 Strength decreased C0003123 Anorexia UMLS C4020887 Photodysphoria C1847024 Albinism, oculocutaneous, type ib (disorder) OrphaNet|HPO|MalaCards C2024878 Cardiovascular surgery result: dyspnea C0549143 Pulmonary renal syndrome MalaCards C1557397 Adverse event associated with pain C0206504 Tympanic membrane perforation HSDN C0085631 Abnormal excitement C0027686 Pathologic neovascularization HSDN C0010201 Cough chronic C0041296 Tuberculosis UMLS C4084766 Vomiting C0043246 Laceration HSDN C4084725 Usual severity cough C0040583 Tracheal stenosis HSDN C0007758 Cerebellar ataxia C2931646 Oculocerebral hypopigmentation syndrome type preus MalaCards C0010038 Corneal opacity disorder C0342895 Fish-eye disease OrphaNet|HPO|MalaCards C0000737 Abdomen pain C2064409 Intrahepatic bile duct cystadenocarcinoma UMLS C0020673 Hypothermia (central) (local) C1704436 Peripheral arterial diseases HSDN C4084802 Usual severity diarrhea C0019099 Hemorrhagic fever, crimean OrphaNet|MalaCards C0917816 Deficiency mental C0035410 Rhabdomyolysis MalaCards C0018991 Paralysis one side of body C0007682 Cns disorder UMLS C1963184 Nystagmus adverse event C0795832 9p tetrasomy MalaCards C0332563 Papulae C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0037383 Sneeze C0028432 Nose diseases HSDN C0036572 Convulsion C0023518 Leukocytosis UMLS C4084788 Have dizziness C0003873 Rheumatoid arthritis HSDN C4084766 Vomiting C2931187 Nephropathic cystinosis MalaCards C0518090 Frequency of pain question C0025521 Inborn errors of metabolism HSDN C1961131 Cough adverse event C0041318 Tuberculosis, meningeal HSDN C4084723 Constipation C0267494 Chilaiditi's syndrome HSDN C0522224 Palsied C0018805 Heart injuries HSDN C0002962 Angina C0030305 Pancreatitis HSDN C2024878 Cardiovascular surgery result: dyspnea C0018023 Nodular goiter HSDN C0232466 Feeding difficulty C4012395 Congenital disorder of glycosylation, type iy MalaCards C1963087 Constipation adverse event C0795864 Smith-magenis syndrome OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0000771 Abnormalities, drug induced HSDN C4085549 Dizziness C0597109 Nurse's role HSDN C0034933 Abnormal reflexes C0006114 Cerebral edema HSDN C3146279 Coma C0023470 Myeloid leukemia HSDN C2919142 Short stature adverse event C1846057 Armfield x-linked mental retardation syndrome OrphaNet|MalaCards C0080274 Retention urinary C0206042 Fatal familial insomnia HPO C0018772 Deafness C2931286 Mosaic variegated aneuplody microcephaly syndrome MalaCards|HPO C0231528 Muscle pain generalized C2931916 Midline granulomatosis MalaCards C0020903 Illusion C0036674 Sensory deprivation HSDN C0030552 Paralysis partial C0342777 Succinate-coenzyme q reductase deficiency MalaCards C0027498 Nausea vomiting C0022660 Kidney failure, acute UMLS C0002962 Angina C0042134 Uterine hemorrhage HSDN C0020305 Fetal edema C0001883 Airway obstruction HSDN C0012833 Dizzy C0346303 Thyrotroph adenoma MalaCards C0015469 Facial paralysis C0001973 Alcoholic intoxication, chronic HSDN C0009080 Finger clubbing C1970431 Pitt-hopkins syndrome MalaCards|HPO C1836296 Lower extremity weakness C0268446 Thyrotoxic periodic paralysis OrphaNet|HPO|MalaCards C0026838 Spasticity muscle C0033348 Language program HSDN C0751295 Memory loss or impairment C0751434 Classical phenylketonuria OrphaNet|HPO|MalaCards C1963064 Anxiety adverse event C1849157 Insulin-like growth factor i, resistance to MalaCards|HPO C0023530 Leukopenia C0282687 Hemorrhagic fever, ebola OrphaNet|MalaCards C3539889 Pelvic pain increasing in severity C0409354 Flexion contracture of hip HSDN C0030794 Pelvis pain C0206622 Adenomyoma HSDN C0151786 Weakness muscle C0020621 Hypokalemia HSDN C0036572 Convulsion C1868546 Patterson pseudoleprechaunism syndrome MalaCards|UMLS C0013362 Dysarthrias C1843807 Basal ganglia disease, biotin-responsive MalaCards|HPO C0000737 Abdomen pain C1711192 Sporadic gastric adenocarcinoma UMLS C1384666 Decreased hearing C1852513 Coxoauricular syndrome OrphaNet|MalaCards C0009806 Constipate C0007194 Hypertrophic cardiomyopathy HSDN C4084774 Have weight loss C0024305 Lymphoma, non-hodgkin HSDN C0241210 Speaking delay C1970199 Mental retardation, autosomal recessive 5 MalaCards|HPO C0151311 Cranial nerve palsy C1868633 Paragangliomas with sensorineural hearing loss HPO C3539020 Pelvic pain decreasing in frequency C0010692 Cystitis HSDN C4084724 Usual severity constipation C0020437 Hypercalcemia HSDN C1962972 Proteinuria adverse event C0007099 Carcinoma in situ HSDN C4084784 Diarrhea C1846172 Hydranencephaly and abnormal genitalia HPO C4085549 Dizziness C0262655 Recurrent urinary tract infection HSDN C0012833 Dizzy C0001807 Aggressive behavior HSDN C0851578 Disorder sleep C0015457 Expression facial HSDN C0015672 Decreased energy C0009324 Ulcerative colitis HSDN C0151686 Growth retardation C1849779 Kowarski syndrome MalaCards C0018681 Headache, cephalalgia C0003864 Arthritis HSDN C0000727 Abdomen acute C0003860 Arteritis HSDN C0473234 Blood in the urine associated with pain C1300028 Disorder characterised by pain UMLS C4085549 Dizziness C0021368 Inflammation HSDN C0015469 Facial paralysis C0037051 Behavior illness HSDN C2984058 Have pain C0162651 Gastric outlet obstruction HSDN C1557397 Adverse event associated with pain C0015409 Eye injuries penetrating HSDN C0019209 Large liver C1136033 Cutaneous mastocytosis MalaCards C0038990 Sweats C0011859 Lipoatrophic diabetes mellitus OrphaNet|HPO C2203646 Jaundice C0024305 Lymphoma, non-hodgkin HSDN C0917816 Deficiency mental C2936502 Charge syndrome, familial MalaCards C1000483 Genus anemia C0268164 Primary hyperoxaluria, type i OrphaNet|HPO C3898969 Have been vomiting C0020522 Delayed hypersensitivity HSDN C0234146 Absent reflex C0795864 Smith-magenis syndrome MalaCards|HPO C4084768 Usual severity vomiting C0022408 Arthropathy HSDN C0023014 Developmental disorder language C0035008 Reinforcement schedules HSDN C0085593 Chill C0398367 Histiocytic necrotizing lymphadenitis HSDN C0242936 Center pain C0740394 Hyperuricemia HSDN C0004604 Pain back C0015579 Family characteristics HSDN C0039870 Leanness C0035009 Reinforcement, social HSDN C4084725 Usual severity cough C0017601 Glaucomas HSDN C0454644 Delayed language development C0684324 Deficiency of phosphoglycerate kinase MalaCards C0151786 Weakness muscle C0029410 Osteoarthritis of hip HSDN C0917816 Deficiency mental C1855348 Marfanoid habitus-microcephaly-glomerulonephritis syndrome MalaCards C1962957 Flushing adverse event C2717899 Upper extremity deep vein thrombosis HSDN C0024031 Back pain lower back C0005967 Bone neoplasms HSDN C2315100 Pediatric failure to thrive C0268548 Hyperargininemia HSDN C2029884 Hearing loss by exam C0027663 Neoplasms, multiple primary HSDN C0037036 Increased salivation C1412397 Ancr gene HPO C0086565 Liver function abnormal C2931471 Sialuria, french type OrphaNet|HPO|MalaCards C0027497 Queasy C0004161 Athletic injuries HSDN C0333243 Edema pitting C0027726 Nephrotic syndrome UMLS C0020450 Hyperemesis gravidarum C0043065 Water electrolyte imbalance HSDN C0150055 Pain chronic C0574960 Sacroiliitis HSDN C2911645 Weight loss adverse event C0031350 Pharyngitis HSDN C0015799 Feminisation C0004898 Beauties HSDN C0242936 Center pain C0013369 Dysentery HSDN C0033774 Skin pruritus C0038987 Sweat gland neoplasms HSDN C3496180 Sleep apnea C0342853 Sialuria OrphaNet|HPO|MalaCards C2032396 Pelvic pain on the right C0037286 Skin neoplasms HSDN C0026821 Cramp C0005491 Biofeedback HSDN C0917816 Deficiency mental C0340834 Hennekam lymphangiectasia lymphedema syndrome MalaCards|HPO C4084724 Usual severity constipation C1833661 Paroxysmal extreme pain disorder OrphaNet|HPO|MalaCards C4084775 Usual severity weight loss C0002878 Anemia, hemolytic HSDN C2984057 Have nausea C0078981 Arachnoid cysts HSDN C0040822 D tremors C0022701 Kinesthesia HSDN C0035078 Failure kidney C0848548 Hypertensive nephropathy MalaCards C4084802 Usual severity diarrhea C0013182 Drug allergy HSDN C0040264 Ear ringing sound C0037286 Skin neoplasms HSDN C0424755 Fever symptoms C0013568 Ecthyma HSDN C0002962 Angina C0038013 Ankylosing spondylitis HSDN C4085211 Pain distress question C1963282 Wolff-parkinson-white syndrome adverse event HSDN C0015469 Facial paralysis C0027667 Cancer origin unknown HSDN C0026826 High muscle tone C0206247 Amyloid neuropathies HSDN C4084773 Bothered by weight gain C0282507 Heat stress disorders HSDN C0011168 Disorder deglutition C1834014 Oculopharyngodistal myopathy MalaCards C0022107 Fussiness C0023381 Letterer-siwe disease MalaCards C0518090 Frequency of pain question C0376634 Craniofacial abnormalities HSDN C4042891 Sleep wake disorders C0004114 Astrocytoma HSDN C1963281 Vomiting adverse event C1963198 Pancreatitis adverse event HSDN C0018834 Brash C0011860 Diabetes mellitus, non-insulin-dependent HSDN C2984058 Have pain C1879338 Bereavement, life event HSDN C0009421 Comatose C0518449 Control of hip fracture risk HSDN C0037771 Paraparesis spastic C0023890 Liver cirrhosis HSDN C1963063 Anorexia adverse event C0086768 Pancreatic cholera OrphaNet|MalaCards C0030193 Sense of pain C0016549 Foreign body reaction HSDN C0008033 Pain pleural C1401747 Quadrilateral fever MalaCards C0018777 Deafness, conductive C1851710 Lateral meningocele syndrome MalaCards|HPO C4084767 Bothered by vomiting C0021390 Inflammatory bowel diseases HSDN C4085317 Diarrhea frequency C0035923 German measles vaccine HSDN C1557397 Adverse event associated with pain C0085605 Liver failure HSDN C0042025 Urinary incontinence stress C0919267 Ovarian neoplasm HSDN C4085317 Diarrhea frequency C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0150055 Pain chronic C0161406 Injury nerve trigeminal HSDN C0007758 Cerebellar ataxia C0752132 Infarction, pca HSDN C0240608 Osler node C0745283 Infectious process UMLS C3887638 Failure to thrive in infant C0008625 Chromosome aberrations HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0020544 Renal hypertension HSDN C0009421 Comatose C3539923 Cdisc adas-cog - orientation summary score HSDN C0022346 Yellow skin C0038395 Streptococcal infections HSDN C0015230 Exanthem C1276071 Childhood atopic dermatitis UMLS C1963281 Vomiting adverse event C0037199 Sinusitis HSDN C3829611 Nausea frequency C0023474 Leukemia, myeloid, chronic-phase HSDN C0018926 Emesis bloody C0007873 Uterine cervical neoplasm HSDN C0085636 Light sensitivity C0037268 Skin abnormalities HSDN C0030193 Sense of pain C1708604 Keratocystic odontogenic tumor UMLS C0004604 Pain back C0006277 Bronchitis HSDN C1384666 Decreased hearing C2937287 Hematolysis HSDN C2032396 Pelvic pain on the right C0018199 Granuloma, plasma cell HSDN C0026821 Cramp C0016169 Pathologic fistula HSDN C1971624 Appetite absent C1706377 Memory device component HSDN C0850758 Pain pelvic C0010695 Cystocele HSDN C2911647 Weight gain adverse event C1135956 Maternal fetal relations HSDN C0042963 Symptoms vomiting C0027627 Neoplasm metastasis HSDN C4084784 Diarrhea C1548777 Specimen reject reason - hemolysis HSDN C0015469 Facial paralysis C0026896 Myasthenia gravis MalaCards C0002170 Alopecia disorders C0162530 Porphyria, erythropoietic HPO C0015672 Decreased energy C0006109 Brain damage, chronic HSDN C0030193 Sense of pain C0009766 Allergic conjunctivitis HSDN C0240715 Perineal lump C0003463 Anus neoplasms UMLS C4084766 Vomiting C0017185 Gastrointestinal neoplasms HSDN C1565249 Limitation, mobility C0029456 Osteoporosis HSDN C1963281 Vomiting adverse event C0276386 Mosquito-borne viral fever, oropouche MalaCards C0027497 Queasy C0009062 Clostridia infection HSDN C0022408 Disorder joint C3672366 Kozlowski celermajer tink syndrome MalaCards C0010200 Cough symptom C1709666 High grade malt lymphoma of the lung UMLS C0020580 Decreased sensation C0085084 Motor neuron disease HSDN C0004134 Dyssynergia C0017658 Glomerulonephritis HSDN C0024031 Back pain lower back C0205788 Histiocytoid hemangioma HSDN C0242936 Center pain C0013592 Ectropion HSDN C0042940 Disorder of voice C1720922 Respiratory aspiration HSDN C0332573 Macula C3826850 Vulvar intraepithelial neoplasia, usual type UMLS C0232462 Appetite decrease C0015624 Fanconi syndrome HPO C0011991 Loose stools C0040034 Thrombocytopenia HSDN C3641756 Have diarrhea C0003496 Aortic rupture HSDN C3898969 Have been vomiting C0013926 Aeroembolism HSDN C2911645 Weight loss adverse event C0033860 Psoriasis HSDN C4085210 Usual severity pain C0022667 Papillary necrosis HSDN C0030193 Sense of pain C3809899 Episodic pain syndrome, familial, 3 MalaCards C4084784 Diarrhea C1956257 Pulmonary stenosis HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0162576 Anisakiasis MalaCards C0278147 Nerve root pain C0522255 Cervical root pain UMLS C0030552 Paralysis partial C0033578 Prostatic neoplasms HSDN C2881387 Visual discomfort, left eye C0015397 Disorder of eye UMLS C0033377 Caudal displacement C0206115 Wagr syndrome OrphaNet|HPO C1549543 Administration method - pain C0006818 Campylobacter infection HSDN C0011991 Loose stools C0267558 Drug and toxin-induced diarrhea UMLS C4018871 Abnormality of the respiratory system C0346072 Blue rubber bleb nevus syndrome MalaCards C2911645 Weight loss adverse event C0013595 Eczema HSDN C0004134 Dyssynergia C0085388 Intracranial tuberculoma HSDN C2315100 Pediatric failure to thrive C0272167 Reticular dysgenesis OrphaNet|HPO|MalaCards C0242936 Center pain C0022904 Lacrimal apparatus diseases HSDN C0038002 Spleen enlargement C0265965 Dyskeratosis congenita MalaCards|HPO C1961131 Cough adverse event C0004114 Astrocytoma HSDN C1963091 Diarrhea adverse event C0005859 Bloom syndrome OrphaNet|HPO|MalaCards C4084769 Vomiting frequency C0243026 Sepsis HSDN C3274924 Have been coughing C0010414 Infection by cryptococcus neoformans HSDN C0011991 Loose stools C0031090 Periodontal diseases HSDN C0015230 Exanthem C1707541 Cutaneous angioimmunoblastic t-cell lymphoma UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0010034 Corneal diseases HSDN C4084768 Usual severity vomiting C0302497 Retrobulbar haemorrhage HSDN C0000737 Abdomen pain C0017105 Clostridial myonecrosis HSDN C1549543 Administration method - pain C0521170 Fracture due to osteoporosis HSDN C0013428 Painful urination C1512737 Infiltrating bladder urothelial carcinoma, clear cell variant UMLS C1557397 Adverse event associated with pain C0009326 Collagen diseases HSDN C0151889 Reflexes tendon increased C0394006 Dysequilibrium syndrome OrphaNet|HPO C0426601 Swallowing symptom nos C4065851 Conversion disorder with swallowing symptoms UMLS C2880344 Corneal deposits in metabolic disorders, right eye C0015397 Disorder of eye UMLS C4084723 Constipation C0021364 Male infertility HSDN C0231528 Muscle pain generalized C0852007 Scleroderma and associated disorders OrphaNet C2919142 Short stature adverse event C1869123 Limb-girdle muscular dystrophy type 2a MalaCards C0042963 Symptoms vomiting C3146297 Study of behavior during childhood HSDN C3898969 Have been vomiting C0917875 Esophageal diverticulosis HSDN C0018991 Paralysis one side of body C0023055 Laryngeal neoplasm HSDN C0013362 Dysarthrias C0006114 Cerebral edema HSDN C0027066 Myoclonic jerking C0012754 Distemper HSDN C0518090 Frequency of pain question C0025958 Microcephaly HSDN C0030193 Sense of pain C0042974 Von willebrand disease HSDN C1963063 Anorexia adverse event C0003469 Anxiety disorders HSDN C0575081 Abnormal gait C1865294 Pelvic hypoplasia with lower-limb arthrogryposis OrphaNet|MalaCards C0017181 Gastrointestinal bleed C0268314 Cholestasis-edema syndrome, norwegian type MalaCards C0917816 Deficiency mental C0406729 Berlin syndrome MalaCards C0015469 Facial paralysis C0023434 Chronic lymphocytic leukemia HSDN C2911645 Weight loss adverse event C0265235 Marshall syndrome MalaCards C0027498 Nausea vomiting C0238198 Gastrointestinal stromal tumors OrphaNet|HPO|MalaCards C0917816 Deficiency mental C1844569 Faciogenital dysplasia with attention deficit-hyperactivity disorder HPO C0518090 Frequency of pain question C0162835 Hypopigmentation disorder HSDN C4084802 Usual severity diarrhea C0012814 Colon nos diverticulitis HSDN C4085317 Diarrhea frequency C0206245 Amyloid neuropathies, familial MalaCards C0010200 Cough symptom C0279706 Lymphoepithelial cancer of thymus UMLS C0015672 Decreased energy C0030305 Pancreatitis HSDN C3541349 Syncope C0263610 Sunlight-induced angio-edema-urticaria OrphaNet|MalaCards C0040264 Ear ringing sound C0032965 Pregnancy complications, infectious HSDN C0028738 Nystagmus C3554605 Mc3dn2 MalaCards C0000737 Abdomen pain C1333741 Adenosquamous carcinoma of gallbladder UMLS C0406146 Meningococcal rash C0009450 Disease caused by microorganism UMLS C1963184 Nystagmus adverse event C3494506 Pseudohypoparathyroidism, type ia OrphaNet|HPO C4084766 Vomiting C0038536 Subcutaneous emphysema HSDN C4085222 Nausea C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C0018681 Headache, cephalalgia C0036330 Schistosomiasis mansoni HSDN C4084775 Usual severity weight loss C1266101 Thymic epithelial tumor OrphaNet C0018772 Deafness C0016658 Fracture bone HSDN C3887873 Hearing loss C0007273 Carotid artery diseases HSDN C0518090 Frequency of pain question C0029442 Osteomalacia HSDN C2919142 Short stature adverse event C1876175 Ataxia-telangiectasia variant MalaCards|HPO C0004604 Pain back C1457883 Aggressive reaction HSDN C0034151 Hyperglobulinemic purpura C0023788 Whipple disease HSDN C4050613 Anxiety C0751434 Classical phenylketonuria MalaCards|HPO C0000727 Abdomen acute C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C2024878 Cardiovascular surgery result: dyspnea C3281234 Combined oxidative phosphorylation deficiency 9 MalaCards C0024031 Back pain lower back C1610547 Production class code - pleasure HSDN C0085636 Light sensitivity C0162361 Hidrotic ectodermal dysplasia OrphaNet|HPO|UMLS C0043094 Weight gain C0036982 Shock, hemorrhagic HSDN C0020305 Fetal edema C0949628 Uniparental disomy HSDN C3641755 Have constipation C0796095 Opitz trigonocephaly syndrome MalaCards|HPO C0013362 Dysarthrias C1851945 Dystonia 1, torsion, autosomal dominant HPO C0018775 Hearing loss bilateral C0018566 Congenital hand deformities HSDN C0015230 Exanthem C0494827 Chronic bullous disease of childhood UMLS C4085210 Usual severity pain C0238190 Inclusion body myositis (disorder) HSDN C0043094 Weight gain C0376550 Astroviridae infection HSDN C0003469 Anxiety disorder C1864112 Huntington disease-like 1 MalaCards|HPO C1549543 Administration method - pain C0039240 Supraventricular tachycardia HSDN C0020538 Hbp C0268074 Indian childhood cirrhosis MalaCards C0151686 Growth retardation C1866504 Photosensitive trichothiodystrophy MalaCards C4085211 Pain distress question C0006736 Body stone HSDN C0018784 Deafness sensorineural C0007194 Hypertrophic cardiomyopathy HSDN C0030193 Sense of pain C0269185 Uterus retroverted HSDN C0027066 Myoclonic jerking C0019202 Hepatolenticular degeneration HSDN C3641756 Have diarrhea C1527429 Increased blood npn HSDN C0085636 Light sensitivity C1836148 Supranuclear palsy, progressive, 2 MalaCards|UMLS C1999266 Depression adverse event C0220704 Shprintzen syndrome MalaCards C0221166 Paraparesis C0022116 Ischemia HSDN C3887873 Hearing loss C1548777 Specimen reject reason - hemolysis HSDN C1963064 Anxiety adverse event C0221406 Pituitary-dependent cushing's disease OrphaNet|HPO C0848203 Male pelvic pain C0007621 Neoplastic cell transformation HSDN C0015468 Face pain C0702221 Tactual discrimination HSDN C1963087 Constipation adverse event C0033246 Proctitis HSDN C0010200 Cough symptom C0003838 Arterial occlusive diseases HSDN C0027498 Nausea vomiting C0342637 Hypocalciuric hypercalcemia, familial, type 1 MalaCards C3665386 Abnormal vision C0221406 Pituitary-dependent cushing's disease HPO C0349588 Stature short C2936859 N syndrome MalaCards C0013456 Pain ear C0020981 Angioimmunoblastic lymphadenopathy HSDN C2029884 Hearing loss by exam C0039128 Syphilis HSDN C0013604 Edematous C1321926 Injury of third cranial nerve HSDN C1963063 Anorexia adverse event C0010709 Cyst HSDN C4085210 Usual severity pain C0275148 Poisoning of animal by plant HSDN C0016199 Pain flank C0278675 Stage i renal cell carcinoma UMLS C0151786 Weakness muscle C1833102 Diabetes mellitus, permanent neonatal, with neurologic features HPO C0018772 Deafness C0030470 Paranasal sinus neoplasms HSDN C4084767 Bothered by vomiting C0014335 Enteritis HSDN C0851578 Disorder sleep C0024919 Behavior, maternal HSDN C1557397 Adverse event associated with pain C0242341 Sexual infantilism HSDN C2984058 Have pain C0752155 Central nervous system vascular malformations HSDN C0027066 Myoclonic jerking C0024776 Maple syrup urine disease HSDN C0424755 Fever symptoms C0275524 Coinfection HSDN C0013404 Respiratory difficulty C0019061 Hemolytic-uremic syndrome HSDN C3887873 Hearing loss C0038395 Streptococcal infections HSDN C0000727 Abdomen acute C0024115 Lung diseases HSDN C2203646 Jaundice C0034069 Pulmonary fibrosis HSDN C0027497 Queasy C0220847 C hepatitis virus HSDN C0037316 Not enough sleeping C0003850 Arteriosclerosis HSDN C0004310 Auditory disorder process C0175702 Williams syndrome HSDN C1069915 Vertigo C0015802 Femur fracture HSDN C0151786 Weakness muscle C0039590 Testicular neoplasms HSDN C0013604 Edematous C0014848 Esophageal achalasia HSDN C0034155 Thrombotic thrombocytopenic purpura C0020951 Immune complex diseases HSDN C0026858 Musculoskeletal pain C0016664 Fatigue fracture HSDN C0040822 D tremors C1837454 Spinocerebellar ataxia 8 MalaCards|HPO|UMLS C0020538 Hbp C3494506 Pseudohypoparathyroidism, type ia HPO C0242936 Center pain C0276275 Disease due to parvoviridae HSDN C0151786 Weakness muscle C0079731 B-cell lymphomas HSDN C0011991 Loose stools C0024694 Mandibular neoplasms HSDN C1510417 Apraxia of gait C1839332 Rett syndrome, preserved speech variant HPO C0027796 Neuralgias C0027819 Neuroblastoma HSDN C1962972 Proteinuria adverse event C0036983 Septic shock HSDN C3641756 Have diarrhea C0051981 Anti-leprosy vaccine HSDN C0009676 Confusion state C0015457 Expression facial HSDN C2984058 Have pain C0162700 Tick-borne diseases HSDN C0424755 Fever symptoms C0079744 Diffuse large b-cell lymphoma HSDN C3898969 Have been vomiting C0376532 Epilepsy, rolandic HSDN C3665386 Abnormal vision C0265313 Weill-marchesani syndrome MalaCards|HPO C0009421 Comatose C1552262 Nurse practitioner - family HSDN C0917816 Deficiency mental C2936741 Syndrome xxyy OrphaNet|MalaCards C0026838 Spasticity muscle C0035078 Kidney failure HSDN C2984058 Have pain C0596263 Carcinogenesis HSDN C0030554 Abnormal sensation C1527336 Sjogren's syndrome HSDN C0011206 Delirium acute C0428953 Ecg infarction myocardial HSDN C0020903 Illusion C0011849 Diabetes mellitus HSDN C3898969 Have been vomiting C0497327 Dementia HSDN C3887873 Hearing loss C0024228 Lymphatic diseases HSDN C0455988 Hydrops fetalis non immune C0268358 Osteogenesis imperfecta, dominant perinatal lethal MalaCards C1384666 Decreased hearing C0039743 Thanatophoric dysplasia OrphaNet|MalaCards C0037763 Spasm C1550639 Specimen type - fistula HSDN C0004134 Dyssynergia C0751039 Cockayne syndrome, type i HPO|UMLS C4084802 Usual severity diarrhea C0039103 Synovitis HSDN C0242936 Center pain C0030286 Pancreatic diseases HSDN C0003811 Cardiac rhythm disturbance C0021368 Inflammation MalaCards C1963093 Dizziness adverse event C0008370 Cholestasis HSDN C0013421 Dystonia C1263846 Attention deficit hyperactivity disorder MalaCards C0795692 Lactate blood increased C0018802 Congestive heart failure HSDN C0028738 Nystagmus C4015307 Perrault syndrome 5 MalaCards C4085210 Usual severity pain C0238198 Gastrointestinal stromal tumors HSDN C0013395 Indigestion C0017563 Gingival diseases HSDN C0020673 Hypothermia (central) (local) C0036118 Salmonella infections, animal HSDN C0030193 Sense of pain C0752140 Intracranial embolism HSDN C0010520 Skin cyanosis C0032087 Plant poisoning HSDN C2984058 Have pain C0043048 Experimental water deprivation HSDN C0030193 Sense of pain C1306710 Facial asymmetry HSDN C4085317 Diarrhea frequency C2926607 Ever told by doctor that you had rheumatic fever:finding:point in time:^patient:ordinal HSDN C4020887 Photodysphoria C0796093 Odontoonychodermal dysplasia MalaCards|HPO C0234512 Prosopagnosia C0020258 Hydrocephalus, normal pressure HSDN C0242936 Center pain C0079774 Peripheral t-cell lymphoma HSDN C1963091 Diarrhea adverse event C0342705 Folate malabsorption, hereditary OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C0023518 Leukocytosis UMLS C2936229 Idiopathic apparent life threatening event C0023976 Long qt syndrome HSDN C0006370 Bulimia C0026785 Munchhausen syndrome HSDN C2984058 Have pain C2028283 History of premature birth HSDN C1384666 Decreased hearing C0013182 Drug allergy HSDN C0002965 Crescendo angina C0024115 Lung diseases HSDN C4050613 Anxiety C1112486 Aggressive systemic mastocytosis OrphaNet|MalaCards C4084802 Usual severity diarrhea C0008325 Cholecystitis HSDN C3898969 Have been vomiting C0015802 Femur fracture HSDN C0851578 Disorder sleep C0018188 Granuloma HSDN C0018681 Headache, cephalalgia C0038271 Stereotyped behavior HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2267227 Bulimia nervosa HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0041330 Tuberculosis, spinal HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024895 Bovine mastitis HSDN C1557397 Adverse event associated with pain C0020502 Hyperparathyroidism HSDN C4084767 Bothered by vomiting C0038463 Strongyloides infection HSDN C0009676 Confusion state C0014057 Japanese encephalitis DiseaseOntology|MalaCards C1963091 Diarrhea adverse event C0026590 Child mother relationship HSDN C0000727 Abdomen acute C0023467 Leukemia, myelocytic, acute HSDN C0751495 Seizure focal C1843140 Seizures, benign familial infantile, 3 MalaCards|HPO|UMLS C0242670 Chronic vegetative state C2937358 Cerebral hemorrhage HSDN C0027796 Neuralgias C1962979 Burn adverse event HSDN C1557397 Adverse event associated with pain C0016879 Fusobacterium infections HSDN C0018989 Paresis of one side of body C2930808 Familial vascular leukoencephalopathy MalaCards C0041657 Consciousness loss C0344434 Atrial fibrillation ecg HSDN C0042024 Urine incontinence C2586211 Thrombosis of blood vessel HSDN C0271215 Blindness legal C1855675 Arima syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0079631 Interdisciplinary communication HSDN C0019825 Voice hoarseness C1336271 Stage iii small cell carcinoma of lung UMLS C0518090 Frequency of pain question C0020523 Immediate hypersensitivity HSDN C0009792 Consciousness disorder C0020635 Hypopituitarism HSDN C0034933 Abnormal reflexes C0424688 Small head HSDN C1328466 Laryngopharyngeal dysesthesia C0544058 Disease or syndrome of laryngopharynx UMLS C0025323 Bleeding menstrual heavy C1866423 Quebec platelet disorder MalaCards|HPO C0004604 Pain back C0600260 Lung diseases, obstructive HSDN C1557397 Adverse event associated with pain C0003486 Aortic aneurysm HSDN C0007859 Pain neck C1532253 Sedentary lifestyle HSDN C1279888 Proteinuria of undiagnosed cause C0000735 Abdominal neoplasms HSDN C0030552 Paralysis partial C2347126 Microscopic polyarteritis HSDN C0042798 Vision dim C0796016 Microphthalmia, syndromic 1 MalaCards|HPO C1963170 Hypothermia adverse event C0006147 Breast fed HSDN C0742313 Chest pain site under breast C0741025 Chest problem UMLS C2919142 Short stature adverse event C0012236 Digeorge syndrome OrphaNet|HPO|MalaCards C3815497 Cough C2239253 Aneurysm of sinus of valsalva MalaCards C1321898 Bloody stool C0019080 Hemorrhage UMLS C0012569 Double vision C0006309 Brucellosis HSDN C0007758 Cerebellar ataxia C0040197 Tick paralysis HSDN C1963281 Vomiting adverse event C0043253 Trauma blunt HSDN C3829611 Nausea frequency C0010074 Coronary vessel anomalies HSDN C1963252 Tremor adverse event C1832903 Migraine, sporadic hemiplegic HPO C1963071 Back pain adverse event C2586211 Thrombosis of blood vessel HSDN C0019825 Voice hoarseness C0022602 Actinic keratosis HSDN C0042963 Symptoms vomiting C0080179 Vertebra fracture HSDN C3898969 Have been vomiting C0042214 Vaccinia HSDN C4084784 Diarrhea C0409959 Osteoarthritis, knee HSDN C0000737 Abdomen pain C0042510 Ventricular fibrillation HSDN C0037384 Snore C0023066 Laryngismus HSDN C0010200 Cough symptom C1253943 Fluid in the chest HSDN C0023380 Lethargy C0026865 Mushroom poisoning HSDN C0040460 Dental pain C0043251 Wounds and injuries HSDN C1384666 Decreased hearing C0086795 Pfaundler-hurler syndrome OrphaNet|HPO C0012569 Double vision C0034067 Pulmonary emphysema HSDN C0240735 Personality change C3160718 Parkinson disease, late-onset MalaCards|HPO C0427190 Ataxia, truncal C1527231 Adrenomyeloneuropathy MalaCards|HPO C0018681 Headache, cephalalgia C0006147 Breast fed HSDN C0349588 Stature short C0268363 Osteogenesis imperfecta type iv (disorder) MalaCards|HPO C0162834 Hyperpigmentation C2749175 Mineralocorticoid deficiency, isolated HPO C3665347 Vision impaired C3179239 Osteopetrosis autosomal dominant type 2 OrphaNet|MalaCards C0231218 Malaise generalized C1332250 Ampulla of vater small cell carcinoma UMLS C0030794 Pelvis pain C0001261 Actinomycosis HSDN C0020305 Fetal edema C0024115 Lung diseases HSDN C0009792 Consciousness disorder C0020875 Ileal diseases HSDN C1963063 Anorexia adverse event C1334968 Nodular lymphocyte predominant hodgkin lymphoma MalaCards C2919142 Short stature adverse event C0268140 Xeroderma pigmentosum, group f HPO C0233514 Behavior abnormal C0751587 Cadasil syndrome HPO C3829611 Nausea frequency C0003855 Arteriovenous fistula HSDN C0008031 Pain chest C0016196 Chest flail HSDN C1961131 Cough adverse event C1565106 Headache disorders, primary HSDN C2032395 Pelvic pain on the left C0021359 Infertility HSDN C0020903 Illusion C1881674 Medical device emits smoke HSDN C0014591 Bleeding nose C0026205 Miosis disorder MalaCards C0036572 Convulsion C1412759 Bckdha gene HSDN C4084802 Usual severity diarrhea C0007095 Carcinoid tumor HSDN C2911645 Weight loss adverse event C0206634 Liposarcoma, myxoid MalaCards C3641755 Have constipation C0000771 Abnormalities, drug induced HSDN C3539895 Pelvic pain occurs with bowel movement C0023890 Liver cirrhosis HSDN C0030193 Sense of pain C0036917 Sexually transmitted diseases, bacterial HSDN C0011991 Loose stools C0268312 Progressive intrahepatic cholestasis (disorder) HPO|UMLS C0042798 Vision dim C1849792 Achromatopsia 3 MalaCards C0003862 Pain joint C3890733 Polyarticular juvenile idiopathic arthritis, rheumatoid factor positive MalaCards C4084775 Usual severity weight loss C0014859 Esophageal neoplasms OrphaNet|HSDN|MalaCards C0413252 Hypothermia due to exposure C0027809 Neurilemmoma HSDN C3146279 Coma C0011570 Mental depression HSDN C0016199 Pain flank C1546533 Specimen source codes - abscess HSDN C1963167 Memory impairment adverse event C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C4085317 Diarrhea frequency C0080178 Spina bifida HSDN C4084723 Constipation C0025312 Meningomyelocele HSDN C0042963 Symptoms vomiting C1546654 Specimen source codes - granuloma HSDN C2096293 Ent surgical result ear vertigo C0040053 Thrombosis HSDN C1961131 Cough adverse event C0043324 Juvenile xanthogranuloma HSDN C3665492 Pigmentations C0750979 Primary malignant neoplasm of brain MalaCards C0042963 Symptoms vomiting C0038941 Incisional infection HSDN C2096293 Ent surgical result ear vertigo C0027809 Neurilemmoma OrphaNet|MalaCards C0426579 Anorexia symptom C0282207 Cronkhite-canada syndrome OrphaNet|MalaCards C0349588 Stature short C2931524 Seemanova-lesny syndrome OrphaNet|MalaCards C0159075 Galacturia C0042075 Urologic diseases UMLS C0018784 Deafness sensorineural C0037199 Sinusitis HSDN C4084768 Usual severity vomiting C0024692 Mandible fracture HSDN C0234471 Conduction aphasia C0018920 Hemangioma, cavernous HSDN C0000737 Abdomen pain C0085278 Antiphospholipid syndrome HSDN C4084802 Usual severity diarrhea C0268328 Porphobilinogen synthase deficiency MalaCards C1961131 Cough adverse event C1299919 Enteric coccidiosis HSDN C4084727 Cough frequency C0205969 Thymic carcinoma OrphaNet|MalaCards C2984058 Have pain C0019069 Hemophilia a HSDN C0030552 Paralysis partial C1999266 Depression adverse event HSDN C0022346 Yellow skin C1336369 Stage ivb carcinoma of liver cells UMLS C0424755 Fever symptoms C0016542 Foreign body HSDN C0497406 Over weight C0032788 Postoperative hemorrhage HSDN C4084725 Usual severity cough C0042075 Urologic diseases HSDN C3494358 Characteristic, prodromal C0003477 Separation anxiety disorder HSDN C0022346 Yellow skin C0001624 Adrenal gland neoplasms HSDN C3274924 Have been coughing C0017178 Gastrointestinal diseases HSDN C0042024 Urine incontinence C0848558 Hypospadias HSDN C0018991 Paralysis one side of body C0009324 Ulcerative colitis HSDN C0016199 Pain flank C0268450 Gitelman syndrome HSDN C0019825 Voice hoarseness C0018802 Congestive heart failure HSDN C4084766 Vomiting C0033778 Vulvar pruritus HSDN C0557874 Global developmental delay C0334123 Histiocytosis, lipoid MalaCards C0497247 Blood pressure elevation C1527168 Bonnevie-ullrich syndrome MalaCards C1963090 Dehydration adverse event C0010418 Cryptosporidiosis DiseaseOntology C0035229 Respiratory function impaired C0010668 Cystic adenomatoid malformation of lung, congenital MalaCards C4084723 Constipation C0014175 Endometriosis HSDN C1963252 Tremor adverse event C0038358 Gastric ulcer HSDN C0003550 Broca aphasia C0812393 Cancer patients and suicide and depression HSDN C0011991 Loose stools C0001418 Adenocarcinoma HSDN C0728710 Pupil constriction observed C0028841 Ocular hypotension HSDN C4085661 Usual severity nausea C0015802 Femur fracture HSDN C1963252 Tremor adverse event C0007959 Charcot-marie-tooth disease HSDN C0042025 Urinary incontinence stress C0005695 Bladder neoplasm HSDN C0018834 Brash C0268335 Ehlers-danlos syndrome type 1 OrphaNet|HPO|MalaCards C0018991 Paralysis one side of body C0037286 Skin neoplasms HSDN C0851578 Disorder sleep C0019326 Ventral hernia HSDN C0030554 Abnormal sensation C0027531 Neck injury HSDN C4084773 Bothered by weight gain C0700208 Acquired scoliosis HSDN C0231835 Respiration rate increased C0004144 Atelectasis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0030569 Secondary parkinson disease HSDN C4085549 Dizziness C0029443 Osteomyelitis HSDN C0012833 Dizzy C0001584 Adolescent psychology HSDN C3541349 Syncope C0149931 Migraine disorders HSDN C3887638 Failure to thrive in infant C2749861 Mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) MalaCards|HPO C0009806 Constipate C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0013428 Painful urination C0855174 Bladder adenocarcinoma, recurrent UMLS C0043094 Weight gain C0002453 Amenorrhea HSDN C0013390 Cramps menstrual C0004936 Mental disorders HSDN C2315100 Pediatric failure to thrive C2931850 Aase smith syndrome 2 MalaCards|HPO C4084723 Constipation C0014356 Enterocolitis HSDN C0039070 Collapse fleeting C0233629 Thinking and speaking disturbances HSDN C4084766 Vomiting C0037315 Sleep apnea syndromes HSDN C0030193 Sense of pain C0014145 Yolk sac tumor HSDN C0013404 Respiratory difficulty C0030581 Parotid neoplasms HSDN C0031911 Pigment deposition C0345905 Intrahepatic cholangiocarcinoma MalaCards C0010520 Skin cyanosis C0023052 Laryngeal edema HSDN C4085548 Usual severity dizziness C0039590 Testicular neoplasms HSDN C4084773 Bothered by weight gain C0011609 Drug eruptions HSDN C4085317 Diarrhea frequency C0037650 Somatoform disorder HSDN C0011991 Loose stools C0006849 Oral candidiasis UMLS C0018681 Headache, cephalalgia C0279748 Lymphoepithelioma, nasopharyngeal UMLS C0151786 Weakness muscle C0175754 Agenesis of corpus callosum HSDN C0020538 Hbp C0376359 Groenblad-strandberg syndrome MalaCards|HPO C0085631 Abnormal excitement C1456784 Paranoia HSDN C3887873 Hearing loss C0024694 Mandibular neoplasms HSDN C0040822 D tremors C0027902 Neuropsychological diagnosis HSDN C0242670 Chronic vegetative state C0027516 Drowning near HSDN C0000727 Abdomen acute C0004096 Asthma HSDN C4085548 Usual severity dizziness C0019372 Herpesviridae infections HSDN C0013395 Indigestion C0020676 Hypothyroidism HSDN C4018871 Abnormality of the respiratory system C1868193 Pneumothorax, primary spontaneous MalaCards C4084775 Usual severity weight loss C0008497 Choriocarcinoma HSDN C0034933 Abnormal reflexes C1138434 Disease, x-linked genetic HSDN C4084784 Diarrhea C0010038 Corneal opacity HSDN C0013456 Pain ear C0011168 Deglutition disorders HSDN C2024893 Cardiovascular surgery result: fatigue C0013010 Cerebral lateralization HSDN C0150055 Pain chronic C0694536 Drug-seeking behavior HSDN C0518090 Frequency of pain question C0018213 Graves disease HSDN C4085862 Bothered by nausea C0149931 Migraine disorders MalaCards C0700590 Diaphoresis excessive C0545044 Acrokeratoelastoidosis of costa OrphaNet|MalaCards C4085549 Dizziness C3827868 Tachycardia by ecg finding HSDN C0043094 Weight gain C0149931 Migraine disorders HSDN C2242996 Tingling C0005659 Bite sting HSDN C2315100 Pediatric failure to thrive C0175693 Russell-silver syndrome HSDN C0042025 Urinary incontinence stress C0007134 Renal cell carcinoma HSDN C0011570 Monopolar depression C0004576 Babesiosis MalaCards C0013421 Dystonia C0751276 Metachromatic leukodystrophy, juvenile type HPO C4084784 Diarrhea C1420653 Tcn2 gene HPO C1963091 Diarrhea adverse event C1553188 Hemolysis - observation HSDN C0039070 Collapse fleeting C0585442 Osteosarcoma of bone HSDN C0030552 Paralysis partial C4015160 Pontocerebellar hypoplasia, type 1c MalaCards C0003079 Pupillary inequality C3809738 Alacrima, achalasia, and mental retardation syndrome MalaCards C0012569 Double vision C0022665 Kidney neoplasm HSDN C0003126 Smell loss C1857720 Kallmann syndrome 4 MalaCards|HPO C0018784 Deafness sensorineural C0795910 Cowchock syndrome MalaCards C0700078 Deep tendon reflex decrease C0752121 Spinocerebellar ataxia type 2 MalaCards|HPO C0018991 Paralysis one side of body C0742479 Cns malignancy meningioma UMLS C4084802 Usual severity diarrhea C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0497406 Over weight C0035455 Rhinitis HSDN C1963252 Tremor adverse event C0040034 Thrombocytopenia HSDN C4084775 Usual severity weight loss C0030499 Parasitic diseases HSDN C2984057 Have nausea C0029185 Orbit tumor HSDN C1263846 Attention deficit disorder with hyperactivity C1859817 2-aminoadipic 2-oxoadipic aciduria HPO C0026821 Cramp C0022104 Irritable bowel syndrome HSDN C0518090 Frequency of pain question C0005683 Urinary bladder calculi (disorder) HSDN C4042891 Sleep wake disorders C0007784 Cerebral hemisphere hemorrhage HSDN C0006370 Bulimia C0020793 Identity crisis HSDN C0878773 Bladder hyperactive C0242350 Erectile dysfunction HSDN C3641755 Have constipation C0030286 Pancreatic diseases HSDN C4085211 Pain distress question C0023646 Lichen planus HSDN C0426579 Anorexia symptom C0162624 Enoplida infection HSDN C0031911 Pigment deposition C1833339 Anophthalmia plus syndrome MalaCards C1557397 Adverse event associated with pain C0010246 Coxsackievirus infections HSDN C3146279 Coma C0162855 Mucinoses HSDN C0007758 Cerebellar ataxia C0272236 Hyperimmunoglobulin m syndrome HSDN C1000483 Genus anemia C3150796 Nephronophthisis 11 MalaCards|HPO C0917816 Deficiency mental C4015619 Epilepsy, progressive myoclonic, 8 MalaCards C0011991 Loose stools C0520946 Emotional hypersensitivity HSDN C4085210 Usual severity pain C1565489 Renal insufficiency HSDN C4085317 Diarrhea frequency C0343387 Enterocolitis, neutropenic HSDN C4084724 Usual severity constipation C1334818 Multicystic mesothelioma of peritoneum MalaCards C1961131 Cough adverse event C0007766 Intracranial aneurysm HSDN C1963071 Back pain adverse event C0236969 Substance-related disorders HSDN C4085211 Pain distress question C0006849 Oral candidiasis HSDN C0020578 Hyperventilate C0030567 Parkinson disease HSDN C0027497 Queasy C0023474 Leukemia, myeloid, chronic-phase HSDN C3887638 Failure to thrive in infant C0524799 Hyperlucent lung HSDN C0036572 Convulsion C0085605 Liver failure MalaCards|HSDN C0024031 Back pain lower back C0024636 Malocclusion HSDN C0023015 Language handicap C0042830 Perception visual HSDN C0034150 Skin purpura C0152025 Polyneuropathy HSDN C1549543 Administration method - pain C0010631 Cystadenocarcinoma HSDN C0277959 Hair coarseness C2930971 Acroosteolysis dominant type MalaCards|HPO C0018772 Deafness C0022758 Kap HSDN C1557397 Adverse event associated with pain C3249881 Infection - suppurative HSDN C3494358 Characteristic, prodromal C0021819 Psychological interview HSDN C0028738 Nystagmus C1849128 Spastic paraplegia 15, autosomal recessive MalaCards|HPO C0042798 Vision dim C0796274 Brown-vialetto-van laere syndrome MalaCards|HPO C4085661 Usual severity nausea C0867389 Chronic graft-versus-host disease MalaCards C4084766 Vomiting C2936858 Congenital adrenal hyperplasia due to 21 hydroxylase deficiency OrphaNet|MalaCards C3898969 Have been vomiting C0717360 Disease lyme vaccine HSDN C3539022 Pelvic pain decreasing in severity C0010692 Cystitis HSDN C0042798 Vision dim C3151086 Retinitis pigmentosa 20 HPO C0344315 Mood depressed C1963674 Spinocerebellar ataxia 10 MalaCards|HPO C4084776 Weight loss C0026636 Mouth diseases HSDN C1962972 Proteinuria adverse event C1857761 Alagille syndrome 2 MalaCards C0747556 Pharyngitis recurrent C3809991 Immunodeficiency, common variable, 10 MalaCards C1549543 Administration method - pain C0014571 Epiphyses, slipped HSDN C0332563 Papulae C0023645 Lichen planus follicularis OrphaNet|MalaCards C0231528 Muscle pain generalized C1853136 Neutral lipid storage disease with myopathy MalaCards|HPO|UMLS C2315100 Pediatric failure to thrive C0006112 Brain diseases, metabolic HSDN C0011991 Loose stools C0859971 Idiopathic diarrhea UMLS C0032617 High urine output C3838758 Familial hyperaldosteronism type 3 MalaCards C0024031 Back pain lower back C0810056 Spondylosis; intervertebral disc disorders; other back problems UMLS C0013378 Dysgensia C0004442 Avoidance learning HSDN C1384666 Decreased hearing C0086651 Mucopolysaccharidosis, mps-iv-a OrphaNet|HPO|MalaCards C0851578 Disorder sleep C0023269 Leiomyosarcoma HSDN C4085211 Pain distress question C0018213 Graves disease HSDN C4084776 Weight loss C0030330 Panniculitis, peritoneal HSDN C0003469 Anxiety disorder C0028860 Oculocerebrorenal syndrome OrphaNet|HPO C4084766 Vomiting C0022650 Kidney calculi HSDN C2984058 Have pain C0016995 Gambling HSDN C0040822 D tremors C0007772 Intracranial arteriovenous malformation HSDN C0019209 Large liver C1418533 Phka2 gene HPO C0030552 Paralysis partial C0010403 Cryoglobulinemia HSDN C1557397 Adverse event associated with pain C0016662 Fracture open HSDN C1963281 Vomiting adverse event C0162666 Mitochondrial encephalomyopathies HSDN C0002170 Alopecia disorders C0079583 Ichthyosiform erythroderma, congenital MalaCards C4084724 Usual severity constipation C0393911 Pure autonomic failure MalaCards C0349588 Stature short C1839332 Rett syndrome, preserved speech variant HPO C0460137 Push down or depress C0001529 Dercum disease OrphaNet|MalaCards C3815497 Cough C0008924 Cleft lip HSDN C0151740 Intracranial hypertension C0206719 Central neurocytoma OrphaNet|MalaCards C0014724 Burping C0560694 Bottles per feed HSDN C4084767 Bothered by vomiting C0012746 Dissociative disorder HSDN C0042025 Urinary incontinence stress C0011854 Diabetes mellitus, insulin-dependent HSDN C3463815 Feel fatigue C0019101 Hemorrhagic fever with renal syndrome OrphaNet|MalaCards C0007166 Cardiac output decreased C0010054 Coronary arteriosclerosis HSDN C0008031 Pain chest C0017086 Gangrene UMLS C4084766 Vomiting C0002989 Epithelioid hemangioma of skin HSDN C0184567 Pain acute C0039584 Testicular diseases HSDN C0242936 Center pain C0521585 Gastrointestinal mucositis HSDN C1963093 Dizziness adverse event C0033054 Prenatal exposure delayed effects HSDN C4050613 Anxiety C0016667 Fragile x syndrome MalaCards|HPO C0000737 Abdomen pain C1334257 Intrahepatic bile duct cystadenoma UMLS C2024878 Cardiovascular surgery result: dyspnea C0006663 Calcinosis HSDN C0013421 Dystonia C4014588 Leukoencephalopathy, progressive, with ovarian failure MalaCards C4084726 Distress cough C1401747 Quadrilateral fever MalaCards C2096293 Ent surgical result ear vertigo C0393735 Headache disorders HSDN C4084773 Bothered by weight gain C0020659 Hypothalamic neoplasms HSDN C0013404 Respiratory difficulty C1708045 Fetal lung adenocarcinoma UMLS C2700617 Irritation - emotion C1112155 Hereditary non-polyposis colorectal cancer syndrome OrphaNet|HPO C4085641 Level of joint pain C3536984 Vitamin d-resistant rickets, x-linked MalaCards C1069915 Vertigo C4048184 Trochlear nerve diseases HSDN C0232488 Colic C0175702 Williams syndrome MalaCards C0424755 Fever symptoms C0015579 Family characteristics HSDN C0518090 Frequency of pain question C0022650 Kidney calculi HSDN C0850758 Pain pelvic C0007137 Squamous cell carcinoma HSDN C0036572 Convulsion C0270819 Cursive epilepsy UMLS C0007758 Cerebellar ataxia C2937358 Cerebral hemorrhage HSDN C0152459 Striae C1857451 Acth-independent macronodular adrenal hyperplasia MalaCards|HPO C3274924 Have been coughing C0030305 Pancreatitis HSDN C0151889 Reflexes tendon increased C0175695 Sotos' syndrome MalaCards|HPO C0015469 Facial paralysis C0020676 Hypothyroidism HSDN C0349588 Stature short C2931737 Hersh podruch weisskopk syndrome MalaCards C4084776 Weight loss C2931242 Familial waldmann's disease MalaCards C0151908 Dry skin C1843355 Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis MalaCards|HPO C0497406 Over weight C0003850 Arteriosclerosis HSDN C4085210 Usual severity pain C0030653 Behavior, paternal HSDN C4085862 Bothered by nausea C0000768 Congenital abnormality HSDN C1963071 Back pain adverse event C0024141 Lupus erythematosus, systemic HSDN C0018926 Emesis bloody C0266015 Congenital digestive system anomalies HSDN C4084726 Distress cough C0040136 Thyroid neoplasm HSDN C1971624 Appetite absent C0003469 Anxiety disorders HSDN C0004604 Pain back C0009917 Contracture HSDN C1963091 Diarrhea adverse event C1863959 Hyperthyroidism, familial gestational OrphaNet|HPO|MalaCards C0917816 Deficiency mental C3280231 Chromosome 8q21.11 deletion syndrome MalaCards C3539895 Pelvic pain occurs with bowel movement C0019553 Contracture hips HSDN C1279888 Proteinuria of undiagnosed cause C0035222 Respiratory distress syndrome, adult HSDN C0857305 Thrombocytopenia purpura C0428953 Ecg infarction myocardial HSDN C0042024 Urine incontinence C2028283 History of premature birth HSDN C0878638 Tongue signs C0221036 Acrodermatitis enteropathica OrphaNet C0019825 Voice hoarseness C0751941 Glossopharyngeal nerve disease or syndrome HSDN C4084725 Usual severity cough C0019195 Hepatitis, viral, human HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0011989 Camurati-engelmann syndrome HSDN C0004604 Pain back C0022658 Kidney diseases HSDN C4084774 Have weight loss C0036117 Salmonella infections HSDN C1549543 Administration method - pain C0038273 Stereotypic movement disorder HSDN C0853945 Oral mucosa blister C0268374 Adult junctional epidermolysis bullosa (disorder) OrphaNet|UMLS|HPO|MalaCards C4084769 Vomiting frequency C0268242 Niemann-pick disease, type a MalaCards|HPO C0038868 Supranuclear palsy progressive C0003873 Rheumatoid arthritis HSDN C1557397 Adverse event associated with pain C3540616 Nci ctep sdc retinoblastoma sub-category terminology HSDN C4084775 Usual severity weight loss C0947622 Cholecystolithiasis HSDN C0853945 Oral mucosa blister C2608084 Epidermolysis bullosa, junctional, localisata variant HPO C0042940 Disorder of voice C0266284 Lingual thyroid HSDN C0007758 Cerebellar ataxia C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards|HPO C0038990 Sweats C3149711 Pheochromocytoma, susceptibility to HPO C2029884 Hearing loss by exam C2117411 X-ray of toe: syndactyly HSDN C0015469 Facial paralysis C0016548 Foreign body migration HSDN C0034933 Abnormal reflexes C0004303 Auditory disease, central HSDN C0042024 Urine incontinence C0014852 Esophageal diseases HSDN C4084776 Weight loss C0020443 Hypercholesterolemia HSDN C0007758 Cerebellar ataxia C2931918 Transketolase defect MalaCards C0085636 Light sensitivity C3887937 Cone dystrophy 5, x-linked MalaCards C3641756 Have diarrhea C0268680 Biotin deficiency MalaCards C0018989 Paresis of one side of body C0744746 Hemiparesis ataxic UMLS C0018772 Deafness C0029464 Osteosclerosis HSDN C0023380 Lethargy C0162637 Strongylida infections HSDN C0027796 Neuralgias C0026896 Myasthenia gravis HSDN C1963281 Vomiting adverse event C2963140 Arteriovenous fistula in use with two needles HSDN C0042963 Symptoms vomiting C0011880 Diabetic ketoacidosis UMLS C0234132 Pyramidal sign C1850568 Nakajo syndrome MalaCards C0848203 Male pelvic pain C0282606 Myomatous neoplasm HSDN C0007815 Cerebrospinal fluid rhinorrhoea C0021400 Influenza HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013595 Eczema HSDN C4084802 Usual severity diarrhea C0042781 Visceral myopathy MalaCards C0024031 Back pain lower back C0027686 Pathologic neovascularization HSDN C2024893 Cardiovascular surgery result: fatigue C0018789 Cardiac aneurysm HSDN C0026838 Spasticity muscle C0752121 Spinocerebellar ataxia type 2 MalaCards|HPO|UMLS C1963281 Vomiting adverse event C1522136 Hypernatremia result HSDN C0751901 Tics vocal C1392622 Chronic motor tics HPO C0036572 Convulsion C0001327 Laryngitis acute HSDN C0008031 Pain chest C0025202 Melanoma HSDN C0036396 Sciatica C0007820 Cerebrovascular disorders HSDN C4084802 Usual severity diarrhea C0029396 Heterotopic ossification HSDN C0004134 Dyssynergia C1412759 Bckdha gene HSDN C0000737 Abdomen pain C0001403 Addison disease OrphaNet|HSDN C0009806 Constipate C2931613 Axial mesodermal dysplasia spectrum OrphaNet|MalaCards C4085548 Usual severity dizziness C0020476 Hyperlipoproteinemias HSDN C0000737 Abdomen pain C0007789 Cerebral palsy HSDN C0018991 Paralysis one side of body C0023470 Myeloid leukemia HSDN C3887638 Failure to thrive in infant C1855101 Methylmalonyl-coa epimerase deficiency with sepiapterin reductase deficiency HPO C0015469 Facial paralysis C0007194 Hypertrophic cardiomyopathy HSDN C0042928 Paralysis vocal cord C0023903 Liver neoplasms HSDN C0034063 Edema lung C0281479 Primary systemic amyloidosis MalaCards C3641756 Have diarrhea C1962971 Myocarditis adverse event HSDN C0030486 Extremity paralysis, lower C0036946 Sheep--diseases HSDN C0042023 Urination frequency C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C3815497 Cough C0153415 Malignant neoplasm of lower third of esophagus MalaCards C1963170 Hypothermia adverse event C0019069 Hemophilia a HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0035923 German measles vaccine HSDN C0033776 Pregnancy and pruritus C0032962 Pregnancy complications UMLS C1963137 Hydrocephalus adverse event C0432364 Accutane dysmorphic syndrome MalaCards C4085210 Usual severity pain C0600041 Infective cystitis HSDN C4084767 Bothered by vomiting C0279606 Childhood hepatocellular carcinoma MalaCards C0007398 Catatonic C1963138 Hypertension adverse event HSDN C0086565 Liver function abnormal C0268314 Cholestasis-edema syndrome, norwegian type MalaCards C2911647 Weight gain adverse event C0031039 Effusion pericardial HSDN C0036572 Convulsion C0001080 Achondroplasia HSDN C1963063 Anorexia adverse event C0001430 Adenoma HSDN C1549543 Administration method - pain C0013363 Dysautonomia HSDN C0017565 Gingiva hemorrhage C0019099 Hemorrhagic fever, crimean MalaCards C0015672 Decreased energy C0005967 Bone neoplasms HSDN C0002962 Angina C0030636 Pasteurella infection HSDN C3463815 Feel fatigue C0025322 Premature menopause HSDN C4084762 Usual severity shortness of breath C0004099 Asthma, exercise-induced MalaCards C4084725 Usual severity cough C0026857 Musculoskeletal diseases HSDN C1549543 Administration method - pain C0024720 Anxiety scale, manifest HSDN C0011991 Loose stools C3668816 Inflammation of non-human mammary gland HSDN C3463815 Feel fatigue C0002940 Aneurysm HSDN C0002962 Angina C0000833 Abscess HSDN C4085549 Dizziness C0035302 Retinal artery occlusion HSDN C3163620 Hypotension adverse event C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C0018784 Deafness sensorineural C0003838 Arterial occlusive diseases HSDN C3146279 Coma C0014065 Congenital cerebral hernia HSDN C1557397 Adverse event associated with pain C0751931 Femoral lesion nerve HSDN C1384666 Decreased hearing C0023895 Liver diseases HSDN C0013421 Dystonia C0524620 Metabolic syndrome x HSDN C0013404 Respiratory difficulty C0022408 Arthropathy HSDN C4084774 Have weight loss C0153413 Malignant neoplasm of upper third of esophagus MalaCards C1961131 Cough adverse event C0027819 Neuroblastoma HSDN C4085317 Diarrhea frequency C0036262 Sarcoptic itch HSDN C0522224 Palsied C1546847 Entity name part type - family HSDN C0018808 Murmur C2673377 Mucolipidosis ii alpha/beta (disorder) HPO C0004134 Dyssynergia C0348165 Viral cns infection HSDN C0018772 Deafness C0085094 Head injury closed HSDN C1557397 Adverse event associated with pain C0003708 Arachnitis HSDN C4084788 Have dizziness C0014457 Eosinophilia HSDN C0080274 Retention urinary C1608393 Megacystis microcolon intestinal hypoperistalsis syndrome MalaCards C3641756 Have diarrhea C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0009806 Constipate C0079744 Diffuse large b-cell lymphoma HSDN C3641756 Have diarrhea C1333976 Hepatic and intrahepatic bile duct neoplasm MalaCards C0024031 Back pain lower back C0011303 Demyelinating diseases HSDN C0086565 Liver function abnormal C1860518 Vasculopathy, retinal, with cerebral leukodystrophy MalaCards|HPO C2315100 Pediatric failure to thrive C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0026838 Spasticity muscle C2931646 Oculocerebral hypopigmentation syndrome type preus MalaCards C0428977 Pulse rate decrease C0018794 Heart block MalaCards C4049602 Hyperactivity C3495551 Dihydropyrimidinuria MalaCards C0015938 Fetal macrosomia C0022876 Premature obstetric labor HSDN C0011991 Loose stools C0021890 Intraoperative complications HSDN C2984058 Have pain C2827407 Infectious otitis media HSDN C0575081 Abnormal gait C0752355 Myotonia fluctuans (disorder) OrphaNet|HPO C0018784 Deafness sensorineural C1862683 Townes brocks branchiootorenal like syndrome HPO C4085222 Nausea C0043253 Trauma blunt HSDN C0018772 Deafness C0015398 Eye diseases, hereditary HSDN C0221232 Welts C0272204 Progressive systemic mastocytosis UMLS C0026838 Spasticity muscle C0040053 Thrombosis HSDN C4085211 Pain distress question C0029899 Otosclerosis HSDN C3539895 Pelvic pain occurs with bowel movement C0033348 Language program HSDN C4085661 Usual severity nausea C1704972 Genomic orientation HSDN C0018772 Deafness C1090821 Sepsis (invertebrate) HSDN C0085593 Chill C0014901 Aesthetic HSDN C0000727 Abdomen acute C0009492 Compartment syndromes HSDN C0011991 Loose stools C0012242 Digestive system disorders HSDN C0746674 Muscle weakness generalized C4014557 Myopathy, tubular aggregate, 2 MalaCards|UMLS C0030200 Intractable pain C2911643 Encounter due to family history of osteoporosis HSDN C0151311 Cranial nerve palsy C0032001 Pituitary apoplexy OrphaNet|MalaCards C0013428 Painful urination C1519929 Vaginal small cell carcinoma UMLS C0085642 Asphyxia reticularis C0020501 Primary hyperoxaluria HSDN C4084802 Usual severity diarrhea C0241910 Hepatitis, autoimmune HSDN C0003962 Ascites C0158683 Polycystic liver disease HPO C3463815 Feel fatigue C0001486 Adenovirus infections HSDN C0003862 Pain joint C1442965 Avascular necrosis of the capital femoral epiphysis MalaCards C3274924 Have been coughing C0153413 Malignant neoplasm of upper third of esophagus MalaCards C0040485 Wryneck C0010278 Craniosynostosis HSDN C1963247 Ventricular tachycardia adverse event C3809536 Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness MalaCards C0085688 Engorgement breast C0157646 Engorgement of breasts associated with childbirth, antepartum condition or complication UMLS C0020450 Hyperemesis gravidarum C0003467 Anxiety HSDN C0010200 Cough symptom C3244301 Coverage level - family HSDN C1963063 Anorexia adverse event C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0016927 Gag reflex C0242952 Behavior infants HSDN C3463815 Feel fatigue C1833372 Hypocalciuric hypercalcemia, familial, type iii MalaCards C0010520 Skin cyanosis C0001327 Laryngitis acute HSDN C3815497 Cough C1836929 Emanuel syndrome MalaCards C4084784 Diarrhea C0152101 Hypoplastic left heart syndrome HSDN C1557397 Adverse event associated with pain C0038579 Substance abuse, intravenous HSDN C4085222 Nausea C1963067 Atrial fibrillation adverse event HSDN C0007166 Cardiac output decreased C0018817 Atrial septal defects HSDN C4084725 Usual severity cough C0038587 Substance withdrawal syndrome HSDN C0019209 Large liver C0221013 Mastocytosis, systemic MalaCards C4084767 Bothered by vomiting C0007131 Non-small cell lung carcinoma HSDN C0014591 Bleeding nose C1861451 Stormorken syndrome MalaCards C1963249 Tinnitus adverse event C3809609 Primary aldosteronism, seizures, and neurologic abnormalities MalaCards C0041657 Consciousness loss C0023895 Liver diseases HSDN C0042571 Vertigo subjective C0151744 Myocardial ischemia HSDN C0040264 Ear ringing sound C1962983 Cataract adverse event HSDN C0242936 Center pain C0007684 Central nervous system infection HSDN C0085636 Light sensitivity C0032453 Polychondritis, relapsing HSDN C0240682 Pelvic girdle pain C0021603 Sleep initiation and maintenance disorders HSDN C1963170 Hypothermia adverse event C0006309 Brucellosis HSDN C0000737 Abdomen pain C1336473 Ovarian polyembryoma stage i UMLS C2911647 Weight gain adverse event C3489393 Hiatal hernia HSDN C0030486 Extremity paralysis, lower C0017636 Glioblastoma HSDN C0018772 Deafness C0221357 Brachydactyly HSDN C0231218 Malaise generalized C0473876 Cryptogenic tularaemia MalaCards C0010520 Skin cyanosis C0149514 Bronchitis acute HSDN C4084769 Vomiting frequency C0031347 Pharyngeal neoplasms HSDN C0557874 Global developmental delay C0432337 Cutis laxa, recessive, type ii OrphaNet C1882272 Pain adverse event by ctcae anatomic descriptor C0005604 Trauma birth HSDN C0085636 Light sensitivity C1852551 Epithelial recurrent erosion dystrophy MalaCards|HPO|UMLS C3887784 Decreased urine output C2072946 Computed tomography of chest: thoracic aortic aneurysm HSDN C0577568 Mass of urinary system structure C1960544 Urethral wart UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0160680 Carotid artery injury HSDN C0040264 Ear ringing sound C0035243 Respiratory tract infections HSDN C3539891 Pelvic pain to the rear C0009404 Colorectal neoplasms HSDN C1963274 Vasculitis adverse event C1328840 Autoimmune lymphoproliferative syndrome MalaCards|HPO C0020639 Hypoproteinaemia C1857338 Deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy MalaCards C0522224 Palsied C3538905 Nci ctep sdc wilms tumor sub-category terminology HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0020179 Huntington disease HSDN C4085317 Diarrhea frequency C0001627 Congenital adrenal hyperplasia HSDN C4084776 Weight loss C0007131 Non-small cell lung carcinoma HSDN C0037763 Spasm C0024299 Lymphoma HSDN C0018681 Headache, cephalalgia C0026266 Mitral valve insufficiency HSDN C0018784 Deafness sensorineural C0002986 Fabry disease MalaCards|HSDN|HPO C0027066 Myoclonic jerking C3539923 Cdisc adas-cog - orientation summary score HSDN C0033377 Caudal displacement C3888138 Monosomy x MalaCards C0011991 Loose stools C0023860 Listeriosis DiseaseOntology|HSDN|MalaCards C0018681 Headache, cephalalgia C0011603 Dermatitis HSDN C0007859 Pain neck C1548578 Location characteristic id - smoking HSDN C0427068 Legs weakness C1853926 Nonaka myopathy OrphaNet C4084769 Vomiting frequency C0020619 Hypogonadism HSDN C0043094 Weight gain C2985290 Fetal alcohol spectrum disorders HSDN C0013404 Respiratory difficulty C0342443 Adrenal cushing's syndrome HSDN C2919142 Short stature adverse event C0265554 Ectrodactyly MalaCards C0018524 Hallucinate C0812393 Cancer patients and suicide and depression HSDN C0018772 Deafness C0029422 Osteochondrodysplasias HSDN C1963091 Diarrhea adverse event C2936797 Acid cholesteryl ester hydrolase deficiency, type 2 OrphaNet C1557397 Adverse event associated with pain C0007860 Uterine cervicitis HSDN C0015672 Decreased energy C0039240 Supraventricular tachycardia HSDN C0010200 Cough symptom C0027983 Newcastle disease DiseaseOntology|MalaCards C4084784 Diarrhea C2939465 Deficiency of glucose-6-phosphate dehydrogenase HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0008073 Developmental disabilities HSDN C2169806 Tic C0013386 Dyskinesia, drug-induced HSDN C2237041 Shox gene with short stature C1840335 Hypomelia mullerian duct anomalies OrphaNet|MalaCards C4084724 Usual severity constipation C0038454 Cerebrovascular accident HSDN C0018772 Deafness C0042510 Ventricular fibrillation HSDN C2237041 Shox gene with short stature C1859305 Cerebellar ataxia and hypogonadotropic hypogonadism HPO C3541349 Syncope C0022890 Labyrinthine disorder HSDN C1963281 Vomiting adverse event C0042580 Vesico-ureteral reflux HSDN C0030552 Paralysis partial C1836076 Amyotrophic lateral sclerosis, chmp2b-related MalaCards C0497406 Over weight C0016470 Food allergy HSDN C0015799 Feminisation C0015696 Fatty liver, alcoholic HSDN C0033377 Caudal displacement C0221759 Brachial plexus neuritis MalaCards C0040264 Ear ringing sound C0005967 Bone neoplasms HSDN C0235778 Dyskinesia neonatal C0013384 Dyskinetic syndrome UMLS C1882272 Pain adverse event by ctcae anatomic descriptor C0023465 Acute monocytic leukemia HSDN C0030193 Sense of pain C0156346 Endometriosis of the rectovaginal septum and vagina nos UMLS C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0220847 C hepatitis virus HSDN C0000737 Abdomen pain C0039981 Thoracic neoplasms HSDN C0557874 Global developmental delay C1327916 Revesz syndrome (disorder) MalaCards|HPO C0578048 Pain of cardiovascular structure C4047625 Pain co-occurrent and due to varicose veins of left leg UMLS C1963071 Back pain adverse event C0039145 Syringomyelia and syringobulbia HSDN C0232466 Feeding difficulty C0079295 Epidermolysis bullosa herpetiformis dowling-meara MalaCards|HPO C1963067 Atrial fibrillation adverse event C1832243 Cardiomyopathy, dilated, 1d (disorder) MalaCards|HPO C0042963 Symptoms vomiting C0268621 Hepatic methionine adenosyltransferase deficiency MalaCards C4085317 Diarrhea frequency C0012811 Colon diverticulum anatomic structure HSDN C0024031 Back pain lower back C0020649 Hypotension HSDN C0019079 Bloody sputum C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0042963 Symptoms vomiting C0018794 Heart block HSDN C0013404 Respiratory difficulty C0040124 Thyroglossal duct cyst HSDN C0270948 Neurogenic muscular atrophy C1839615 Myopathy, x-linked, with excessive autophagy (disorder) MalaCards|HPO C2911645 Weight loss adverse event C0030920 Peptic ulcer HSDN C0151686 Growth retardation C4014258 Immunodeficiency, common variable, 11 MalaCards C0020672 Body temperature decreased C0003838 Arterial occlusive diseases HSDN C1549543 Administration method - pain C1963235 Sick sinus syndrome adverse event HSDN C0030486 Extremity paralysis, lower C0030271 Pancoast syndrome HSDN C4085210 Usual severity pain C0041972 Urethral obstruction HSDN C0018772 Deafness C0039231 Tachycardia HSDN C1319543 On examination - right eye diabetic maculopathy C0011849 Diabetes mellitus UMLS C4084775 Usual severity weight loss C0149841 Benign recurrent intrahepatic cholestasis OrphaNet C1963087 Constipation adverse event C0015663 Fasting HSDN C0018681 Headache, cephalalgia C0007274 Carotid artery thrombosis HSDN C0033774 Skin pruritus C0406300 Dermographic prurigo UMLS C0018784 Deafness sensorineural C2751312 Bartter syndrome, type 4b HPO C2024893 Cardiovascular surgery result: fatigue C0030297 Pancreatic neoplasm HSDN C0085636 Light sensitivity C1865869 Cone dystrophy 3 (disorder) HPO C1963252 Tremor adverse event C0004030 Aspergillosis HSDN C0232861 Penis discharge C0741437 Male_repro problem UMLS C4084775 Usual severity weight loss C0751161 Udpglucose 4-epimerase deficiency disease OrphaNet|MalaCards C0030193 Sense of pain C0001122 Acidosis HSDN C0019079 Bloody sputum C0024299 Lymphoma HSDN C0042798 Vision dim C0152177 Trigeminal neuropathy HSDN C0231807 Dyspnea exertional C2931787 Intracardiac myxoma MalaCards C4085548 Usual severity dizziness C0031350 Pharyngitis HSDN C0042963 Symptoms vomiting C0264766 Rheumatic mitral stenosis HSDN C0013456 Pain ear C0031024 Suppurative periapical periodontitis HSDN C1963093 Dizziness adverse event C0032914 Pre-eclampsia HSDN C0015970 Fever unknown origin C0027667 Cancer origin unknown HSDN C0013604 Edematous C0005586 Bipolar disorder HSDN C0009806 Constipate C0007121 Bronchogenic carcinoma HSDN C0018808 Murmur C0032962 Pregnancy complications HSDN C4084776 Weight loss C0700208 Acquired scoliosis HSDN C1549543 Administration method - pain C0949691 Spondylarthropathies HSDN C1963164 Lymphopenia adverse event C0267372 Intestinal lymphatic obstruction OrphaNet|MalaCards C1557397 Adverse event associated with pain C1253943 Fluid in the chest HSDN C0151786 Weakness muscle C0175816 Cold hemagglutinin disease OrphaNet|MalaCards C0040822 D tremors C0751583 Encephalitis, west nile fever DiseaseOntology|MalaCards C0751837 Gait ataxic C0677050 Manganese poisoning HSDN C4084788 Have dizziness C0018798 Congenital heart defects HSDN C2984058 Have pain C0038940 Surgical wound dehiscence HSDN C2024893 Cardiovascular surgery result: fatigue C0034194 Pyloric stenosis HSDN C0030552 Paralysis partial C0040115 Thymus hyperplasia HSDN C0042798 Vision dim C1834329 Retinitis pigmentosa 27 MalaCards|HPO C2984057 Have nausea C3539923 Cdisc adas-cog - orientation summary score HSDN C4084725 Usual severity cough C0003949 Asbestosis HSDN C4084784 Diarrhea C0039128 Syphilis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0162835 Hypopigmentation disorder HSDN C0235153 Sensory hallucination C0751279 Metachromatic leukodystrophy, adult-type (disorder) HPO C1963164 Lymphopenia adverse event C2931241 Primary intestinal lymphangiectasis OrphaNet|MalaCards C0028961 Urine output decreased C0018965 Hematuria HSDN C2984058 Have pain C0039981 Thoracic neoplasms HSDN C0036572 Convulsion C0085648 Synovial cyst HSDN C0038002 Spleen enlargement C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C1313921 Urinomas C0043254 Injuries penetrating HSDN C2032395 Pelvic pain on the left C0042065 Genitourinary neoplasms HSDN C4085661 Usual severity nausea C0010709 Cyst HSDN C0557874 Global developmental delay C0729582 Floating-harbor syndrome OrphaNet|HPO|MalaCards C0036572 Convulsion C0339852 Dermoids nasal MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0027831 Neurofibromatosis 1 HSDN C4085862 Bothered by nausea C0556520 Psychological desensitization HSDN C3641756 Have diarrhea C0035412 Rhabdomyosarcoma HSDN C4020887 Photodysphoria C1851841 Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 1 OrphaNet|HPO C0043068 Friderichsen-waterhouse syndrome C0001118 Acid base imbalance HSDN C1557397 Adverse event associated with pain C0040261 Onychomycosis HSDN C0009421 Comatose C0027831 Neurofibromatosis 1 HSDN C4084802 Usual severity diarrhea C0025299 Meningocele HSDN C0009676 Confusion state C0018916 Hemangioma HSDN C0018777 Deafness, conductive C2930793 Achondroplastic dwarfism MalaCards C4084784 Diarrhea C0006264 Bronchial neoplasms HSDN C3898969 Have been vomiting C0004943 Behcet syndrome HSDN C4049644 Depression C2748910 Rett syndrome, atypical MalaCards C0015672 Decreased energy C0002792 Anaphylaxis HSDN C3641756 Have diarrhea C0031347 Pharyngeal neoplasms HSDN C1963091 Diarrhea adverse event C0870082 Hyperkeratosis HSDN C0042571 Vertigo subjective C0854906 Benign schwannoma OrphaNet|MalaCards C0000727 Abdomen acute C2984299 Asthma pathway HSDN C0009806 Constipate C1563705 Nephrogenic diabetes insipidus, type i HPO|UMLS C0030193 Sense of pain C0011119 Decompression sickness HSDN C3641756 Have diarrhea C0206692 Carcinoma, lobular HSDN C2024893 Cardiovascular surgery result: fatigue C0017160 Gastroenteritis HSDN C0150055 Pain chronic C0011334 Dental caries HSDN C0027066 Myoclonic jerking C0019693 Hiv infections HSDN C2919142 Short stature adverse event C0920349 Sponastrime MalaCards C1963091 Diarrhea adverse event C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0015469 Facial paralysis C0001175 Acquired immunodeficiency syndrome HSDN C0151205 Periorbital edema C1290857 Disorder of face UMLS C0239589 Finger pain C2896450 Pain in hand and fingers UMLS C0009806 Constipate C0011581 Depressive disorder HSDN C3665492 Pigmentations C1261274 Keratoconjunctivitis due to mycoplasma conjunctivae MalaCards C0022346 Yellow skin C0004623 Bacterial infections HSDN C2315100 Pediatric failure to thrive C0242597 Leukocyte-adhesion deficiency syndrome HSDN C3541349 Syncope C0042594 Vestibular diseases HSDN C0018772 Deafness C1850040 Pelviscapular dysplasia OrphaNet|HPO|MalaCards C0040034 Thrombocytopenia C0398367 Histiocytic necrotizing lymphadenitis MalaCards C0018775 Hearing loss bilateral C0016508 Congenital foot deformity HSDN C0518090 Frequency of pain question C0025309 Meningoencephalitis HSDN C0013456 Pain ear C0017671 Glomus jugulare tumor HSDN C4085661 Usual severity nausea C0037286 Skin neoplasms HSDN C1963177 Muscle pain adverse event C1853136 Neutral lipid storage disease with myopathy MalaCards C0015672 Decreased energy C0027643 Neoplasm recurrence, local HSDN C0037763 Spasm C0151998 Spasm uterine UMLS C1963281 Vomiting adverse event C0085389 Bacillaceae infection HSDN C0009806 Constipate C0018523 Hallervorden-spatz syndrome OrphaNet|MalaCards C0011991 Loose stools C0022568 Keratitis HSDN C4085661 Usual severity nausea C0276357 Swine influenza MalaCards C0009398 Color vision defects C4014856 Cone-rod dystrophy 20 MalaCards C0018681 Headache, cephalalgia C0018213 Graves disease HSDN C1962972 Proteinuria adverse event C0162871 Aortic aneurysm, abdominal HSDN C0917816 Deficiency mental C2673874 Bardet biedl syndrome 14 (disorder) MalaCards|HPO C1263846 Attention deficit disorder with hyperactivity C1504412 Testotoxicosis MalaCards|HPO C0917816 Deficiency mental C2936921 Saccharopine dehydrogenase deficiency MalaCards C0030552 Paralysis partial C3811918 Grn-related frontotemporal dementia MalaCards C4085211 Pain distress question C0752242 Limitus, hallux HSDN C0013456 Pain ear C0006325 Bruxism HSDN C1963093 Dizziness adverse event C0017601 Glaucomas HSDN C0039070 Collapse fleeting C3150943 Long qt syndrome 2 MalaCards|HPO|UMLS C0003126 Smell loss C0393778 Congenital anosmia MalaCards|UMLS C4085222 Nausea C0024841 Matrimony, matrimonial HSDN C1384666 Decreased hearing C0019054 Hemolysis (disorder) HSDN C0018772 Deafness C0017921 Glycogen storage disease type ii MalaCards|HPO C1963091 Diarrhea adverse event C0023788 Whipple disease OrphaNet|MalaCards C2911645 Weight loss adverse event C0553580 Ewings sarcoma HSDN C0000737 Abdomen pain C0003123 Anorexia UMLS C0086565 Liver function abnormal C0017922 Glycogen storage disease type iii HPO C0037317 Sleep disturbance C0270972 Cornelia de lange syndrome OrphaNet|HPO|MalaCards C1860844 Sparse, thin hair C3279807 Ced3 MalaCards C0019825 Voice hoarseness C1879314 Poorly differentiated ovarian sertoli-leydig cell tumor UMLS C0151786 Weakness muscle C0037313 Sleep HSDN C0518090 Frequency of pain question C0032064 Plague HSDN C0043144 Wheeze C0155882 Intrinsic asthma + status UMLS C4085211 Pain distress question C0701818 Choledocholithiasis HSDN C0027066 Myoclonic jerking C0220847 C hepatitis virus HSDN C4084726 Distress cough C0042830 Perception visual HSDN C4084724 Usual severity constipation C2239176 Liver carcinoma HSDN C4084802 Usual severity diarrhea C3541899 Nci ctep sdc osteosarcoma sub-category terminology HSDN C0003126 Smell loss C1969607 Kallmann syndrome 2 with selective tooth agenesis HPO C0030200 Intractable pain C0026650 Movement disorders HSDN C0917816 Deficiency mental C0795989 Hypospadias-mental retardation syndrome MalaCards C0751295 Memory loss or impairment C0011644 Scleroderma MalaCards C0851578 Disorder sleep C0000786 Spontaneous abortion HSDN C0009460 Communication impairment C1720777 Functional laterality HSDN C0085602 Polydypsia C0023788 Whipple disease MalaCards C0018772 Deafness C0010276 Craniopharyngioma MalaCards|HPO C0042755 Virilisation C0812393 Cancer patients and suicide and depression HSDN C4084784 Diarrhea C0027540 Necrosis HSDN C0009806 Constipate C0010709 Cyst HSDN C4020887 Photodysphoria C1857588 Amaurosis hypertrichosis OrphaNet|HPO|MalaCards C1963087 Constipation adverse event C1421143 Trh gene HPO C0424755 Fever symptoms C0018213 Graves disease HSDN C0013390 Cramps menstrual C0027651 Tumor HSDN C0028738 Nystagmus C0206247 Amyloid neuropathies MalaCards C0026821 Cramp C0004935 Animal ethology HSDN C0006370 Bulimia C2609414 Acute kidney injury HSDN C0037763 Spasm C0005747 Blepharospasm UMLS C0035078 Failure kidney C3543867 Collodion fetus MalaCards C0413252 Hypothermia due to exposure C0376618 Endotoxemia HSDN C0013404 Respiratory difficulty C0023269 Leiomyosarcoma HSDN C0413252 Hypothermia due to exposure C0032326 Pneumothorax HSDN C1384666 Decreased hearing C1852542 Cdo syndrome MalaCards C4084788 Have dizziness C0033893 Tension headache HSDN C0028738 Nystagmus C1849115 Spastic paraplegia 5a, autosomal recessive (disorder) MalaCards C0003550 Broca aphasia C0027051 Myocardial infarction HSDN C2984058 Have pain C0016436 Folliculitis HSDN C0007398 Catatonic C0078981 Arachnoid cysts HSDN C0751188 Dural headache post puncture C1302110 Headache post myelography UMLS C0040034 Thrombocytopenia C1856448 Bernard soulier syndrome, type c HPO C4084727 Cough frequency C0011644 Scleroderma OrphaNet|MalaCards C3463815 Feel fatigue C0018995 Hemochromatosis OrphaNet C1549543 Administration method - pain C0041341 Tuberous sclerosis HSDN C0037315 Breathing disorder during sleeping C0410529 Hypochondroplasia (disorder) MalaCards|HPO C3274924 Have been coughing C3178892 Disease, pelvic floor HSDN C2024878 Cardiovascular surgery result: dyspnea C0036323 Schistosomiasis HSDN C0522224 Palsied C0393799 Miller fisher syndrome HSDN C0030486 Extremity paralysis, lower C0001122 Acidosis HSDN C0151889 Reflexes tendon increased C4014347 Pontocerebellar hypoplasia, type 10 MalaCards C4084773 Bothered by weight gain C0016563 Form perception HSDN C4084768 Usual severity vomiting C0268581 Holocarboxylase synthetase deficiency MalaCards|HPO C1963091 Diarrhea adverse event C0015652 Fascioliasis HSDN C0851578 Disorder sleep C2981150 Uranostaphyloschisis HSDN C4085211 Pain distress question C0027645 Neoplasm seeding HSDN C0042963 Symptoms vomiting C0023521 Globoid cell leukodystrophy MalaCards|HPO|UMLS C0010200 Cough symptom C3179093 Injuries, laryngeal nerve HSDN C0557874 Global developmental delay C4014435 Mental retardation, autosomal dominant 26 MalaCards C1963071 Back pain adverse event C0002895 Anemia, sickle cell HSDN C0008031 Pain chest C1266101 Thymic epithelial tumor OrphaNet C0027796 Neuralgias C0029463 Osteosarcoma HSDN C1963087 Constipation adverse event C0559260 Congenital scoliosis HSDN C4084802 Usual severity diarrhea C0015480 Disorder factitious HSDN C0043352 Absent salivary secretion C0281479 Primary systemic amyloidosis MalaCards C0013404 Respiratory difficulty C0018824 Heart valve disease HSDN C0038990 Sweats C1835663 Keratosis palmaris et plantaris with clinodactyly OrphaNet|MalaCards C0018681 Headache, cephalalgia C1333760 Gasserian ganglion meningioma UMLS C2024893 Cardiovascular surgery result: fatigue C3810814 Myocardial infarction ecg assessment HSDN C4084726 Distress cough C0005779 Blood coagulation disorders HSDN C0406406 Persisting cholinergic urticaria C0021368 Inflammation UMLS C1963170 Hypothermia adverse event C1522136 Hypernatremia result HSDN C2024893 Cardiovascular surgery result: fatigue C0271737 Addison's disease due to autoimmunity OrphaNet C1557397 Adverse event associated with pain C2004487 Vaginal spasm HSDN C2926613 Chest pain:finding:point in time:^patient:ordinal C0037579 Soft tissue neoplasms HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0153066 Murray valley encephalitis DiseaseOntology|MalaCards C0028081 Night sweat C0855087 Nodular sclerosis hodgkin's disease stage i UMLS C4084725 Usual severity cough C0018193 Granuloma, foreign-body HSDN C0030794 Pelvis pain C0023890 Liver cirrhosis HSDN C0030975 Disorders perception C0032787 Postoperative complications HSDN C0518090 Frequency of pain question C0010967 Behavior, dangerous HSDN C0518090 Frequency of pain question C0701818 Choledocholithiasis HSDN C0239574 Fever low grade C0036231 Sarcocystosis DiseaseOntology C0003469 Anxiety disorder C1853445 Parkinson disease 7, autosomal recessive early-onset MalaCards|HPO C0497247 Blood pressure elevation C1863340 Pituitary adenoma predisposition (disorder) HPO C0037383 Sneeze C4084909 Depression subordinate domain HSDN C0027066 Myoclonic jerking C0027927 Neurosyphilis HSDN C4084776 Weight loss C4050407 Pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis MalaCards C0003811 Cardiac rhythm disturbance C2931785 Juvenile dermatomyositis MalaCards C4084768 Usual severity vomiting C0700095 Central neuroblastoma HSDN C4084788 Have dizziness C0033968 Psychotherapeutic technique HSDN C0018784 Deafness sensorineural C2931008 Congenital disorder of glycosylation type 2a MalaCards|HPO C0023015 Language handicap C0020550 Hyperthyroidism HSDN C2048468 Inability to impregnate C0010674 Cystic fibrosis MalaCards|HPO C0000737 Abdomen pain C0854782 Stage ii rectosigmoid cancer UMLS C0008031 Pain chest C0027051 Myocardial infarction UMLS C0018834 Brash C3806730 Mental retardation, x-linked 98 MalaCards C0018681 Headache, cephalalgia C1552262 Nurse practitioner - family HSDN C0040822 D tremors C0432474 Klinefelter's syndrome - male with more than two x chromosomes HSDN C4084784 Diarrhea C0016542 Foreign body HSDN C4085642 Level of joint stiffness C0029455 Osteopoikilosis (disorder) MalaCards C0013144 Drowsy C0032858 Powassan encephalitis MalaCards C1962972 Proteinuria adverse event C0039006 Swine--diseases HSDN C3539023 Pelvic pain increasing in frequency C0269185 Uterus retroverted HSDN C4084773 Bothered by weight gain C0037397 Behavior social HSDN C0349588 Stature short C2931557 Chromosome 4 short arm deletion MalaCards C0237326 Defecation pain C1563705 Nephrogenic diabetes insipidus, type i HPO C0812426 Kidney problem C0011881 Diabetic nephropathy UMLS C0007758 Cerebellar ataxia C1290398 Cerebral arterial aneurysm HSDN C0026838 Spasticity muscle C0003850 Arteriosclerosis HSDN C0037763 Spasm C0011849 Diabetes mellitus HSDN C0013604 Edematous C1456865 Ureteral calculi HSDN C1971624 Appetite absent C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0026884 Muteness C0007784 Cerebral hemisphere hemorrhage HSDN C4084784 Diarrhea C0343528 Legionella pneumophila; infection, nonpneumonic MalaCards C3463815 Feel fatigue C1963134 Hemorrhoids adverse event HSDN C4084776 Weight loss C0027686 Pathologic neovascularization HSDN C4084802 Usual severity diarrhea C0042510 Ventricular fibrillation HSDN C0022408 Disorder joint C1859372 Calcification of joints and arteries MalaCards|HPO C0036572 Convulsion C2750220 Karak syndrome MalaCards|HPO C0043094 Weight gain C0016658 Fracture bone HSDN C0022568 Inflammation corneal C1337030 Xpa gene HPO C0427055 Face weakness C1834569 Jankovic rivera syndrome MalaCards|HPO|UMLS C4084773 Bothered by weight gain C0034885 Rectal neoplasms HSDN C0018926 Emesis bloody C0019123 Hemothorax HSDN C4042891 Sleep wake disorders C0011168 Deglutition disorders HSDN C0518090 Frequency of pain question C0085110 Severe combined immunodeficiency HSDN C0022346 Yellow skin C0305062 Tetanus toxoids HSDN C0016204 Fart C0009375 Colonic neoplasms HSDN C4084784 Diarrhea C0025309 Meningoencephalitis HSDN C0018524 Hallucinate C0018809 Heart neoplasm HSDN C4084775 Usual severity weight loss C0001486 Adenovirus infections HSDN C1961131 Cough adverse event C1837218 Cleft palate, isolated HSDN C0018772 Deafness C0582587 Visual learning HSDN C0043094 Weight gain C0152054 Therapeutic touch HSDN C0917816 Deficiency mental C1857512 Temtamy syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C1334272 Invasive apocrine breast carcinoma UMLS C2024878 Cardiovascular surgery result: dyspnea C0024530 Malaria HSDN C0700590 Diaphoresis excessive C0334419 Pheochromocytoma, malignant MalaCards C4084723 Constipation C0041107 Trisomy HSDN C0917816 Deficiency mental C0268524 Gamma-glutamyltransferase deficiency MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0014457 Eosinophilia HSDN C0012569 Double vision C1579931 Depressed - symptom HSDN C3146279 Coma C0021670 Insulinoma MalaCards|HPO C0005745 Blepharoptosis C3809490 Chromosome 3q13.31 deletion syndrome MalaCards C4085210 Usual severity pain C0002884 Hypochromic anemia HSDN C0034933 Abnormal reflexes C0012746 Dissociative disorder HSDN C0003811 Cardiac rhythm disturbance C2931850 Aase smith syndrome 2 OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C0042514 Tachycardia, ventricular HSDN C0917816 Deficiency mental C3541471 Mitochondrial complex iii deficiency, nuclear type 1 MalaCards C0042963 Symptoms vomiting C0040411 Tongue neoplasms HSDN C0151889 Reflexes tendon increased C0342765 D-glyceric aciduria HPO C0011991 Loose stools C1832370 Myopathy, myofibrillar, desmin-related MalaCards|HPO C0497406 Over weight C0007784 Cerebral hemisphere hemorrhage HSDN C1963091 Diarrhea adverse event C0002949 Aneurysm, dissecting HSDN C1384666 Decreased hearing C1275079 Acps iii MalaCards C0242936 Center pain C0041325 Peritonitis, tuberculous MalaCards|HSDN C0037384 Snore C0032914 Pre-eclampsia HSDN C0042510 Fibrillation paroxysmal vent C3150943 Long qt syndrome 2 MalaCards|HPO C0039070 Collapse fleeting C0001418 Adenocarcinoma HSDN C0018524 Hallucinate C0266526 Norrie disease MalaCards|HPO C0018775 Hearing loss bilateral C0028738 Nystagmus HSDN C0231341 Aging premature C0086543 Cataract nos HSDN C3463815 Feel fatigue C0040809 Patient refusal of treatment HSDN C4084726 Distress cough C0013295 Duodenal ulcer HSDN C0015230 Exanthem C0033771 Prurigo UMLS C1313921 Urinomas C0041955 Ureteral neoplasms HSDN C0019209 Large liver C0268255 Farber lipogranulomatosis OrphaNet|HPO|MalaCards C2129634 Fecal incontinence with formed stools C0015732 Fecal incontinence UMLS C0040822 D tremors C0275148 Poisoning of animal by plant HSDN C0518090 Frequency of pain question C0022364 Jaw neoplasms HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C2945560 Hemolytic HSDN C2096293 Ent surgical result ear vertigo C0037937 Spine injury HSDN C4084766 Vomiting C0027583 Nematode infections HSDN C0040259 Tinea pedis C0162627 Skin diseases, bacterial HSDN C4050613 Anxiety C0175702 Williams syndrome OrphaNet|HPO|MalaCards C3274924 Have been coughing C0040583 Tracheal stenosis HSDN C0043094 Weight gain C0006261 Bronchial diseases HSDN C4085211 Pain distress question C0008698 Maxillary sinusitis chronic HSDN C1384666 Decreased hearing C1860224 Ablepharon-macrostomia syndrome OrphaNet|HPO|MalaCards C0013456 Pain ear C0009197 Cochlear diseases HSDN C0349588 Stature short C1837822 Burn-mckeown syndrome MalaCards|HPO C0242936 Center pain C0560694 Bottles per feed HSDN C1963087 Constipation adverse event C0036202 Sarcoidosis HSDN C1963274 Vasculitis adverse event C0034152 Henoch-schoenlein purpura OrphaNet|MalaCards C0000737 Abdomen pain C0206743 Rhabdoid tumor OrphaNet|MalaCards C0152459 Striae C0041324 Tuberculosis, osteoarticular HSDN C0009676 Confusion state C3810814 Myocardial infarction ecg assessment HSDN C1557397 Adverse event associated with pain C2219717 Menstrual periods stopped for over 6 months HSDN C4084802 Usual severity diarrhea C0022758 Kap HSDN C2048468 Inability to impregnate C1504412 Testotoxicosis OrphaNet|HPO|MalaCards C0033377 Caudal displacement C4015643 Combined oxidative phosphorylation deficiency 24 MalaCards C0013604 Edematous C0019557 Hip fx HSDN C4085210 Usual severity pain C0022593 Keratosis HSDN C0011991 Loose stools C0003184 Anthropology HSDN C2029884 Hearing loss by exam C0242422 Parkinsonian disorders HSDN C3463815 Feel fatigue C0282207 Cronkhite-canada syndrome OrphaNet|MalaCards C0518090 Frequency of pain question C0032797 Postpartum hemorrhage HSDN C0085636 Light sensitivity C1835851 Ichthyosis with hypotrichosis, autosomal recessive MalaCards|UMLS C0013404 Respiratory difficulty C0085084 Motor neuron disease HSDN C4085549 Dizziness C0271375 Cranial nerve palsy iv trochlear HSDN C0019214 Hepatosplenomegaly C0152061 Louse-borne relapsing fever, nos DiseaseOntology|MalaCards C0024032 Birth weight subnormal C0268418 Deficiency of glycerol kinase MalaCards|HPO C0015469 Facial paralysis C0520946 Emotional hypersensitivity HSDN C1963170 Hypothermia adverse event C0001721 Emotional affect HSDN C0587048 Upper extremity mass C1527349 Ductal breast carcinoma UMLS C2132198 Abnormal blistering of the skin C0406369 Lichen planus pemphigoides MalaCards C0242936 Center pain C0017168 Gastroesophageal reflux disease HSDN C1384666 Decreased hearing C0022410 Joint instability HSDN C2029884 Hearing loss by exam C0206526 Tuberculosis, multidrug-resistant HSDN C0009676 Confusion state C0024121 Lung neoplasms HSDN C2315100 Pediatric failure to thrive C1968556 Encephalopathy, neonatal severe, due to mecp2 mutations HPO C0020450 Hyperemesis gravidarum C2981150 Uranostaphyloschisis HSDN C4085548 Usual severity dizziness C1414203 Dws gene HSDN C4085548 Usual severity dizziness C0020443 Hypercholesterolemia HSDN C0018834 Brash C1866958 Laryngeal and pharyngeal hypoplasia with omphalocele MalaCards C0036572 Convulsion C0016510 Foot diseases HSDN C0031911 Pigment deposition C1333156 Classic fibrosarcoma MalaCards C1963167 Memory impairment adverse event C1866855 Spastic paraplegia 4, autosomal dominant MalaCards|HPO C2242996 Tingling C0206245 Amyloid neuropathies, familial HSDN C0042025 Urinary incontinence stress C0041755 Adverse reaction to drug HSDN C0043094 Weight gain C0042140 Uterine prolapse HSDN C0019572 Hairiness C1845530 Stocco dos santos syndrome MalaCards C0034150 Skin purpura C0919267 Ovarian neoplasm HSDN C0008031 Pain chest C1962979 Burn adverse event HSDN C1971624 Appetite absent C0020538 Hypertensive disease HSDN C4085211 Pain distress question C0008325 Cholecystitis HSDN C0424755 Fever symptoms C0023798 Lipoma HSDN C1963252 Tremor adverse event C0751122 Infantile severe myoclonic epilepsy OrphaNet|HPO C1549543 Administration method - pain C0004044 Asphyxia HSDN C0013362 Dysarthrias C0043251 Wounds and injuries HSDN C2315100 Pediatric failure to thrive C0431406 Asymmetric crying face association HPO C0041105 Jaw spasm C0796176 Stuve-wiedemann syndrome OrphaNet|HPO C4084726 Distress cough C3540583 Nci ctep sdc neuroblastoma sub-category terminology HSDN C2984058 Have pain C0003492 Aortic coarctation HSDN C4084776 Weight loss C3661523 Congenital intestinal aganglionosis OrphaNet|HPO|MalaCards C1000483 Genus anemia C0342739 Trimethylaminuria MalaCards|HPO C0042571 Vertigo subjective C1136041 Familial acoustic neuroma OrphaNet|HPO C1963087 Constipation adverse event C0042251 Vaginal diseases HSDN C3815497 Cough C2911643 Encounter due to family history of osteoporosis HSDN C1519353 Skin eruption papular C0268397 Amyloidosis, primary cutaneous MalaCards C0878773 Bladder hyperactive C0812393 Cancer patients and suicide and depression HSDN C4085661 Usual severity nausea C0000768 Congenital abnormality HSDN C0085606 Urination urgency C1868595 Parkinson disease 1, autosomal dominant (disorder) HPO C0497406 Over weight C0018482 Haemophilus infections HSDN C4084784 Diarrhea C0000821 Threatened abortion HSDN C4084776 Weight loss C2239290 Hodgkin lymphoma, nodular lymphocyte predominance MalaCards C0030794 Pelvis pain C1458155 Mammary neoplasms HSDN C0015230 Exanthem C0343771 Human ehrlichiosis MalaCards C0518090 Frequency of pain question C0029429 Osteochondrosis HSDN C0007166 Cardiac output decreased C0020625 Hyponatremia HSDN C0013421 Dystonia C2748910 Rett syndrome, atypical MalaCards|HPO C0030975 Disorders perception C0007786 Brain ischemia HSDN C0010200 Cough symptom C1336184 Stage iib large cell carcinoma of lung UMLS C3665347 Vision impaired C0282527 Infantile refsum disease (disorder) OrphaNet|HPO|MalaCards C4049602 Hyperactivity C0268126 Adenylosuccinate lyase deficiency (disorder) MalaCards|HPO C0009806 Constipate C0019112 Hemorrhoids UMLS C0012833 Dizzy C0006818 Campylobacter infection HSDN C0018772 Deafness C0037417 Identification, social HSDN C0018772 Deafness C0022660 Kidney failure, acute HSDN C0019521 Hiccoughs C0034088 Pulmonary valve insufficiency HSDN C4084769 Vomiting frequency C0305062 Tetanus toxoids HSDN C0557874 Global developmental delay C3810080 Mental retardation, autosomal recessive 40 MalaCards C0518090 Frequency of pain question C0037824 Intelligibilities, speech HSDN C0020580 Decreased sensation C0752130 Spinal cord ischemia HSDN C0009398 Color vision defects C2350521 Gustatory perception HSDN C4085210 Usual severity pain C0035585 Rickettsia infections HSDN C2315100 Pediatric failure to thrive C0015668 Fat necrosis HSDN C0031315 Phantom limb pain C0031118 Peripheral nervous system neoplasms HSDN C0007814 Cerebrospinal fluid otorrhea C3203359 Rupture HSDN C2024878 Cardiovascular surgery result: dyspnea C0281479 Primary systemic amyloidosis MalaCards C2024878 Cardiovascular surgery result: dyspnea C0027726 Nephrotic syndrome HSDN C0022107 Fussiness C3489725 Pseudo-torch syndrome MalaCards C0023380 Lethargy C0027404 Narcolepsy HSDN C0030193 Sense of pain C0019087 Hemorrhagic disorders HSDN C1963281 Vomiting adverse event C0024236 Lymphedema HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0023290 Leishmaniasis, visceral HSDN C2919142 Short stature adverse event C1968739 Glycogen storage disease iiia HPO C0007859 Pain neck C0033578 Prostatic neoplasms HSDN C2237041 Shox gene with short stature C1838348 Oculomaxillofacial dysostosis OrphaNet|MalaCards C4042891 Sleep wake disorders C0019348 Herpes simplex infections HSDN C2362324 Pediatric obesity C0030767 Grouping peer HSDN C3539896 Pelvic pain occurs with urination C0010709 Cyst HSDN C3146279 Coma C2931832 Hyperinsulinemic hypoglycemia, familial, 1 MalaCards C0004604 Pain back C0042029 Urinary tract infection HSDN C4084768 Usual severity vomiting C0011860 Diabetes mellitus, non-insulin-dependent HSDN C0015970 Fever unknown origin C2926063 Myocardial infarction:finding:point in time:^patient:ordinal HSDN C4084774 Have weight loss C0027022 Myeloproliferative disease HSDN C0042024 Urine incontinence C0029458 Osteoporosis, postmenopausal HSDN C3146279 Coma C1704972 Genomic orientation HSDN C0004134 Dyssynergia C0599412 Lordosis [mating posture] HSDN C0005745 Blepharoptosis C1832390 Van maldergem wetzburger verloes syndrome MalaCards|HPO C3641755 Have constipation C0206718 Ganglioneuroblastoma HSDN C0003862 Pain joint C0008728 Churg-strauss syndrome OrphaNet|HSDN|MalaCards C3539893 Pelvic pain occurs with intercourse C0314657 Genetic predisposition HSDN C0041657 Consciousness loss C0042510 Ventricular fibrillation HSDN C2919142 Short stature adverse event C1866505 Ichthyosis, congenital, with trichothiodystrophy HPO C0033774 Skin pruritus C0030757 Pediculus capitis infestation DiseaseOntology C0015970 Fever unknown origin C0085073 Prosthesis-related infection HSDN C4085210 Usual severity pain C0017168 Gastroesophageal reflux disease HSDN C3665346 Loss sight C0346388 Malignant melanoma of choroid OrphaNet|HPO C3898969 Have been vomiting C0042870 Vitamin d deficiency HSDN C0010200 Cough symptom C1709781 Pyothorax-associated lymphoma UMLS C1549543 Administration method - pain C0025268 Multiple endocrine neoplasia type 2a HSDN C0451941 Itch scrotum C0406623 Skin disorder of penis and scrotum UMLS C2911647 Weight gain adverse event C0027707 Nephritis, interstitial HSDN C0460137 Push down or depress C0085209 Bovine spongiform encephalitis MalaCards C1557397 Adverse event associated with pain C0012746 Dissociative disorder HSDN C0152459 Striae C0035309 Retinal diseases HSDN C3641756 Have diarrhea C1856143 Hemolytic uremic syndrome, typical MalaCards C3641755 Have constipation C1833661 Paroxysmal extreme pain disorder OrphaNet|HPO|MalaCards C4085210 Usual severity pain C0857007 Hyperbilirubinemia, neonatal HSDN C3541349 Syncope C0027516 Drowning near HSDN C0235153 Sensory hallucination C1850451 Ceroid lipofuscinosis, neuronal, 1 MalaCards|HPO C0013404 Respiratory difficulty C0038354 Stomach diseases HSDN C2029884 Hearing loss by exam C0040053 Thrombosis HSDN C0042963 Symptoms vomiting C0346290 Benign tumor choroid plexus UMLS C1253937 Pericardial effusion C0085090 Lymphoma, aids-related MalaCards C1963091 Diarrhea adverse event C0033289 Family relationship, professional HSDN C0221184 Hemianopsia bitemporal C1336537 Supratentorial meningioma MalaCards C0030193 Sense of pain C0018206 Granulosa cell tumor HSDN C3463815 Feel fatigue C0009373 Colonic diseases HSDN C2315100 Pediatric failure to thrive C0017178 Gastrointestinal diseases HSDN C0016199 Pain flank C0042075 Urologic diseases HSDN C0013608 Cardiac edema C0011175 Dehydration HSDN C4085210 Usual severity pain C0024636 Malocclusion HSDN C4085548 Usual severity dizziness C1962963 Osteoporosis adverse event HSDN C0008031 Pain chest C0860603 Anxiety symptoms HSDN C0013604 Edematous C1547046 Kind of quantity - taste HSDN C0011991 Loose stools C0005424 Biliary tract diseases HSDN C0004941 Behavioral symptoms C1849722 Polyglucosan body disease, adult form OrphaNet|HPO|MalaCards C0039070 Collapse fleeting C1299262 Sarcoma - category (morphologic abnormality) HSDN C0002170 Alopecia disorders C1852278 Deafness-craniofacial syndrome MalaCards C2132198 Abnormal blistering of the skin C0432313 Epidermolysis bullosa simplex with hypodontia OrphaNet|MalaCards C4085222 Nausea C0024141 Lupus erythematosus, systemic HSDN C4084727 Cough frequency C0036467 Scrofula MalaCards C0497406 Over weight C0003811 Cardiac arrhythmia HSDN C0033774 Skin pruritus C0020544 Renal hypertension HSDN C0497247 Blood pressure elevation C0152171 Idiopathic pulmonary hypertension HPO C2984057 Have nausea C0031039 Effusion pericardial HSDN C1963170 Hypothermia adverse event C1720777 Functional laterality HSDN C2984057 Have nausea C0014836 Escherichia coli infections HSDN C0020455 Hypergammaglobulinemia C0026976 Myelitis, transverse HSDN C4084767 Bothered by vomiting C0751285 Maple syrup urine disease, thiamine responsive HPO C3829611 Nausea frequency C0027686 Pathologic neovascularization HSDN C3539895 Pelvic pain occurs with bowel movement C0038160 Staphylococcal infections HSDN C0557874 Global developmental delay C3711387 Autosomal recessive primary microcephaly OrphaNet|HPO|MalaCards C0004604 Pain back C2609414 Acute kidney injury HSDN C0018784 Deafness sensorineural C1854273 Radioulnar synostosis with amegakaryocytic thrombocytopenia HPO C0349588 Stature short C3280054 Geleophysic dysplasia 2 MalaCards C3898969 Have been vomiting C0751285 Maple syrup urine disease, thiamine responsive HPO C0030554 Abnormal sensation C0494491 Mononeuropathies HSDN C1961131 Cough adverse event C0024299 Lymphoma HSDN C0037316 Not enough sleeping C0003618 Appetites HSDN C0034124 Pupillary disorder C2937358 Cerebral hemorrhage HSDN C0036659 Sensation disorder C0004096 Asthma HSDN C0041105 Jaw spasm C0022661 Kidney failure, chronic HSDN C0009024 Clonus C0162671 Melas syndrome OrphaNet|HPO|MalaCards C0030193 Sense of pain C0152174 Somatoform pain disorder UMLS C0424755 Fever symptoms C0042075 Urologic diseases HSDN C0242936 Center pain C0008073 Developmental disabilities HSDN C0013378 Dysgensia C0007762 Cerebellar neoplasms HSDN C1963170 Hypothermia adverse event C0403447 Chronic kidney insufficiency HSDN C1963249 Tinnitus adverse event C3839212 Familial hyperaldosteronism type 2 MalaCards C3815497 Cough C0040583 Tracheal stenosis HSDN C0242936 Center pain C0043167 Pertussis HSDN C0497406 Over weight C0019163 Hepatitis b HSDN C4084766 Vomiting C0027819 Neuroblastoma HSDN C2911647 Weight gain adverse event C0020523 Immediate hypersensitivity HSDN C2919142 Short stature adverse event C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C4084784 Diarrhea C0004933 Behavior modification technique HSDN C1145670 Failure respiratory C3280679 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset MalaCards C4085317 Diarrhea frequency C0032002 Pituitary diseases HSDN C0034155 Thrombotic thrombocytopenic purpura C0023903 Liver neoplasms HSDN C4084727 Cough frequency C3489393 Hiatal hernia HSDN C0030193 Sense of pain C0017510 Gestures HSDN C4085210 Usual severity pain C0007894 Cestode infections HSDN C0424755 Fever symptoms C0024282 Lymphocytosis HSDN C0032227 Effusion pleural C0041327 Tuberculosis, pulmonary MalaCards C4084767 Bothered by vomiting C0344315 Depressed mood HSDN C4085210 Usual severity pain C1704421 Skin pigmentation disorder HSDN C2128090 Dip joint of left middle toe feels loose C1862103 Brachydactyly type c MalaCards C0043068 Friderichsen-waterhouse syndrome C0031046 Pericarditis HSDN C4084775 Usual severity weight loss C0001883 Airway obstruction HSDN C0151686 Growth retardation C0268119 Combined molybdoflavoprotein enzyme deficiency HPO C4084774 Have weight loss C0039590 Testicular neoplasms HSDN C1963087 Constipation adverse event C0004238 Atrial fibrillation HSDN C1860844 Sparse, thin hair C0406355 Acrokeratosis paraneoplastica of bazex MalaCards C1963091 Diarrhea adverse event C0024638 Class ii division 2 malocclusion HSDN C0004604 Pain back C0019348 Herpes simplex infections HSDN C3539890 Pelvic pain causes awakening at night C1961100 Erectile dysfunction adverse event HSDN C2919142 Short stature adverse event C1849334 Robinow syndrome, autosomal recessive MalaCards|HPO C0557874 Global developmental delay C3713418 Ppm-x syndrome MalaCards C0232462 Appetite decrease C0153459 Malignant neoplasm of body of pancreas MalaCards C0009421 Comatose C0021831 Intestinal diseases HSDN C0221263 Cafe au lait spot C1969623 Neurofibromatosis, type 1-like syndrome MalaCards|HPO C0007758 Cerebellar ataxia C1858054 Bardet-biedl syndrome 6 HPO C0042571 Vertigo subjective C0010276 Craniopharyngioma MalaCards|HPO C4084769 Vomiting frequency C1553188 Hemolysis - observation HSDN C3539893 Pelvic pain occurs with intercourse C1548578 Location characteristic id - smoking HSDN C0031911 Pigment deposition C0268425 Alstrom syndrome MalaCards C4085862 Bothered by nausea C0349464 Wernicke-korsakoff syndrome HSDN C1963091 Diarrhea adverse event C2931189 Neural crest tumor MalaCards C1549543 Administration method - pain C0022366 Jaw, edentulous HSDN C0030193 Sense of pain C3863028 Left trigeminal neuralgia UMLS C2203646 Jaundice C1546847 Entity name part type - family HSDN C0041657 Consciousness loss C0013712 Ego HSDN C0016199 Pain flank C0206651 Sarcoma, clear cell HSDN C3887873 Hearing loss C0041408 Turner syndrome HSDN C0013604 Edematous C0011608 Dermatitis herpetiformis MalaCards C0349588 Stature short C0543816 Cardiocutaneous syndrome MalaCards C1549543 Administration method - pain C0039082 Syndrome HSDN C0039231 Heartbeats increased C1860471 Stoll alembik dott syndrome MalaCards C0000737 Abdomen pain C1553188 Hemolysis - observation HSDN C0242936 Center pain C0001815 Primary myelofibrosis HSDN C0027497 Queasy C0010074 Coronary vessel anomalies HSDN C4084802 Usual severity diarrhea C0035127 Cumulative trauma disorders HSDN C2237041 Shox gene with short stature C0022716 Menkes kinky hair syndrome MalaCards|HPO C0010200 Cough symptom C0854982 Stage iv large cell carcinoma of lung UMLS C0838224 Pain in a joint, forearm C0810055 Other non-traumatic joint disorders UMLS C1549543 Administration method - pain C2108112 Continuous electrocardiogram ventricular fibrillation HSDN C0000731 Abdomen distention C0043208 Wolman disease OrphaNet|HPO C1963065 Apnea adverse event C3150986 Epileptic encephalopathy, early infantile, 7 MalaCards C0042963 Symptoms vomiting C0268581 Holocarboxylase synthetase deficiency MalaCards|HPO|UMLS C0518090 Frequency of pain question C0026272 Mixed connective tissue disease HSDN C2911647 Weight gain adverse event C0262655 Recurrent urinary tract infection HSDN C0040822 D tremors C0014121 Bacterial endocarditis HSDN C0042571 Vertigo subjective C0395938 Aplasia of the cochlea and vestibular labyrinth UMLS C4084766 Vomiting C1956346 Coronary artery disease HSDN C0237326 Defecation pain C1561866 Congenital central alveolar hypoventilation syndrome MalaCards C3463815 Feel fatigue C0018099 Gout HSDN C0018772 Deafness C3151445 Dyskeratosis congenita, autosomal dominant, 3 MalaCards|HPO C1963281 Vomiting adverse event C4049644 Depression HSDN C0013421 Dystonia C3502054 Dentoleukoencephalopathy MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0334409 Leydig cell tumor, benign HSDN C0015970 Fever unknown origin C0011849 Diabetes mellitus HSDN C0009806 Constipate C1881674 Medical device emits smoke HSDN C3815497 Cough C0206141 Idiopathic hypereosinophilic syndrome HSDN C3665386 Abnormal vision C0796070 Microphthalmia, syndromic 7 MalaCards C0023380 Lethargy C0268467 Hyperphenylalaninemia, bh4-deficient, b MalaCards|HPO|UMLS C0034933 Abnormal reflexes C0010068 Coronary heart disease HSDN C0042571 Vertigo subjective C0038941 Incisional infection HSDN C4085211 Pain distress question C0206647 Dermatofibrosarcoma HSDN C4085210 Usual severity pain C3163843 Chondrosarcoma of bone HSDN C0019825 Voice hoarseness C0002949 Aneurysm, dissecting HSDN C1961131 Cough adverse event C0022758 Kap HSDN C0162285 Edema eyelid C2751321 Macrocephaly, alopecia, cutis laxa, and scoliosis HPO C0750323 Vomit intractable C0746781 Nausea intractable UMLS C3829611 Nausea frequency C0013502 Echinococcosis HSDN C0002962 Angina C0027658 Neoplasms, germ cell and embryonal HSDN C0042963 Symptoms vomiting C0013449 Ear neoplasms HSDN C0015469 Facial paralysis C0524910 Hepatitis c, chronic HSDN C0020673 Hypothermia (central) (local) C0010054 Coronary arteriosclerosis HSDN C2984058 Have pain C0039373 Tay-sachs disease HSDN C4085317 Diarrhea frequency C0043168 Whooping cough due to unspecified organism HSDN C0000727 Abdomen acute C0033968 Psychotherapeutic technique HSDN C0162298 Stiffness joints C1833699 Osteopoikilosis, isolated MalaCards|HPO C0020505 Excessive eating C3813158 Experimental organism islet cell adenoma neoplasm MalaCards C2029884 Hearing loss by exam C0027092 Myopia HSDN C0151786 Weakness muscle C0003504 Aortic valve insufficiency HSDN C0009421 Comatose C0001118 Acid base imbalance HSDN C0037763 Spasm C1096903 Sialic acid storage disease, finnish type (disorder) MalaCards C0010200 Cough symptom C0033923 Psychomotor function HSDN C3641755 Have constipation C0266209 Congenital dilatation of colon MalaCards C4084723 Constipation C0007820 Cerebrovascular disorders HSDN C0012833 Dizzy C0023890 Liver cirrhosis HSDN C1963071 Back pain adverse event C0007570 Celiac disease HSDN C1145670 Failure respiratory C1864669 Neuronal ceroid lipofuscinosis due to cathepsin d deficiency MalaCards|HPO C2024893 Cardiovascular surgery result: fatigue C1333990 Hereditary nonpolyposis colorectal cancer OrphaNet|HPO|MalaCards C0152228 Diplacusis, unspecified ear C0271509 Diplacusis, echo UMLS C0013390 Cramps menstrual C0001144 Acne vulgaris HSDN C3714552 Strength decreased C0343633 Brazilian haemorrhagic fever MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0010073 Coronary artery vasospasm HSDN C0040034 Thrombocytopenia C3151205 Megaloblastic anemia due to dihydrofolate reductase deficiency MalaCards|HPO C1290771 Edema of oral vestibule C0459146 Disorder of soft tissue of body cavity UMLS C0009806 Constipate C0009324 Ulcerative colitis HSDN C0009806 Constipate C0002878 Anemia, hemolytic HSDN C1963087 Constipation adverse event C1275081 Cardio-facio-cutaneous syndrome HPO C0242936 Center pain C0022667 Papillary necrosis HSDN C0917816 Deficiency mental C1857342 Deafness, cochlear, with myopia and intellectual impairment HPO C1565249 Limitation, mobility C0085433 Acquired joint deformities HSDN C2984058 Have pain C0001118 Acid base imbalance HSDN C0036572 Convulsion C0032045 Placenta disorders HSDN C3463815 Feel fatigue C0038579 Substance abuse, intravenous HSDN C0522224 Palsied C0020523 Immediate hypersensitivity HSDN C2237041 Shox gene with short stature C1850331 Oculorenocerebellar syndrome OrphaNet|MalaCards C3146279 Coma C0020179 Huntington disease HSDN C0027796 Neuralgias C0019348 Herpes simplex infections HSDN C2984058 Have pain C0004044 Asphyxia HSDN C4084725 Usual severity cough C1532560 Plasmacytoma - category HSDN C0042963 Symptoms vomiting C0002874 Aplastic anemia HSDN C0018772 Deafness C0026771 Trauma multiple HSDN C0151825 Ostalgia C0013366 Dyschondroplasia OrphaNet|HPO|MalaCards C4085862 Bothered by nausea C1704212 Embolism embolus HSDN C0013604 Edematous C0038644 Sudden infant death syndrome HSDN C0184567 Pain acute C1419157 Pygm gene HSDN C2237041 Shox gene with short stature C0023234 Legg-calve-perthes disease OrphaNet|HPO|MalaCards C0497406 Over weight C0004936 Mental disorders HSDN C0020455 Hypergammaglobulinemia C0002874 Aplastic anemia HSDN C0038506 Stutter C1552262 Nurse practitioner - family HSDN C0857305 Thrombocytopenia purpura C1299262 Sarcoma - category (morphologic abnormality) HSDN C4084769 Vomiting frequency C0001175 Acquired immunodeficiency syndrome HSDN C0040034 Thrombocytopenia C0580190 3-phosphoglycerate dehydrogenase deficiency MalaCards C1557397 Adverse event associated with pain C0030421 Paraganglioma HSDN C0039070 Collapse fleeting C0026769 Multiple sclerosis HSDN C0019079 Bloody sputum C0264458 Chemical pneumonitis MalaCards C0026838 Spasticity muscle C3813607 Infantile gastroesophageal reflux HSDN C0021359 Infertility C2751325 46,xy gonadal dysgenesis, partial, with minifascicular neuropathy OrphaNet|HPO C0030552 Paralysis partial C0038220 Status epilepticus HSDN C4084767 Bothered by vomiting C1547044 Kind of quantity - smell HSDN C4085211 Pain distress question C0043540 Zygomatic fracture HSDN C0013378 Dysgensia C0751941 Glossopharyngeal nerve disease or syndrome HSDN C2984058 Have pain C0235032 Neurotoxicity syndromes HSDN C3539889 Pelvic pain increasing in severity C0030455 Parametritis HSDN C0036572 Convulsion C0342257 Complications of diabetes mellitus HSDN C0028738 Nystagmus C3150998 Spinocerebellar ataxia, autosomal recessive 10 MalaCards|HPO C0042963 Symptoms vomiting C0239189 Disaccharide intolerance MalaCards C2024893 Cardiovascular surgery result: fatigue C1963083 Cholecystitis adverse event HSDN C0026838 Spasticity muscle C0004623 Bacterial infections HSDN C4020887 Photodysphoria C2749685 Cystinosis, atypical nephropathic (disorder) HPO C0042025 Urinary incontinence stress C0022658 Kidney diseases HSDN C0019080 Bleed_nos problem C1853278 Bleeding disorder due to p2ry12 defect MalaCards C4084784 Diarrhea C0242658 Homosexuality male HSDN C3641755 Have constipation C0221043 Liddle syndrome OrphaNet|HPO|MalaCards C0027796 Neuralgias C2609414 Acute kidney injury HSDN C0004604 Pain back C0018273 Growth disorders HSDN C2984058 Have pain C0007124 Noninfiltrating intraductal carcinoma HSDN C0413252 Hypothermia due to exposure C0027643 Neoplasm recurrence, local HSDN C2984058 Have pain C0026916 Mycobacterium avium-intracellulare infection HSDN C0009792 Consciousness disorder C0007684 Central nervous system infection HSDN C1999266 Depression adverse event C1839780 Fragile x tremor/ataxia syndrome OrphaNet|HPO|MalaCards C1549543 Administration method - pain C0024954 Maxillary neoplasms HSDN C0020673 Hypothermia (central) (local) C0040127 Thyroid crisis HSDN C0700078 Deep tendon reflex decrease C2751319 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 MalaCards|HPO C0036572 Convulsion C1848578 Methylmalonic aciduria and homocystinuria, cblf type (disorder) OrphaNet|HPO|MalaCards C2911647 Weight gain adverse event C0600041 Infective cystitis HSDN C1962972 Proteinuria adverse event C3469186 Hemochromatosis, type 1 HSDN C0231528 Muscle pain generalized C0039082 Syndrome HSDN C0018772 Deafness C0042164 Uveitis HSDN C0036659 Sensation disorder C0080174 Spina bifida occulta HSDN C0231528 Muscle pain generalized C0178842 Sensory feedback HSDN C2237041 Shox gene with short stature C0265267 Congenital hemidysplasia with ichthyosiform erythroderma and limb defects HPO C0018772 Deafness C1690964 Cataract HSDN C0024031 Back pain lower back C0004030 Aspergillosis HSDN C1557397 Adverse event associated with pain C0005426 Biliary tract neoplasm HSDN C4085548 Usual severity dizziness C0000768 Congenital abnormality HSDN C0518090 Frequency of pain question C0517555 Venous thrombosis after immobility HSDN C0034150 Skin purpura C0008370 Cholestasis HSDN C4084769 Vomiting frequency C0019372 Herpesviridae infections HSDN C0030193 Sense of pain C0023892 Biliary cirrhosis HSDN C1384666 Decreased hearing C0026706 Mucopolysaccharidosis iii OrphaNet|MalaCards C1963252 Tremor adverse event C2827407 Infectious otitis media HSDN C0007758 Cerebellar ataxia C0878675 Erdheim-chester disease MalaCards|HSDN C0030193 Sense of pain C0042376 Vascular headaches HSDN|UMLS C1549543 Administration method - pain C0015405 Fungal eye infections HSDN C0751837 Gait ataxic C1857747 Neurodegeneration with brain iron accumulation 2 (disorder) MalaCards|HPO|UMLS C0150055 Pain chronic C0023890 Liver cirrhosis HSDN C3814874 Loss of appetite question C0035288 Reticuloendotheliosis, x-linked MalaCards C4084768 Usual severity vomiting C0013595 Eczema HSDN C2984058 Have pain C0036899 Abstinence sex HSDN C1963091 Diarrhea adverse event C0867389 Chronic graft-versus-host disease MalaCards C4085862 Bothered by nausea C0001418 Adenocarcinoma HSDN C0002962 Angina C1963274 Vasculitis adverse event HSDN C0030193 Sense of pain C0029882 Otitis media HSDN C2024893 Cardiovascular surgery result: fatigue C3163620 Hypotension adverse event HSDN C2984057 Have nausea C0017160 Gastroenteritis DiseaseOntology|HSDN C0018784 Deafness sensorineural C0012979 Canine disease HSDN C4084767 Bothered by vomiting C1854698 Multiple carboxylase deficiency, juvenile-onset MalaCards|HPO C0439814 Prickling C0030554 Paresthesia UMLS C0013604 Edematous C3814778 Hemolytic index HSDN C0030554 Abnormal sensation C1762616 Meningioma, benign, no icd-o subtype HSDN C0013604 Edematous C0524620 Metabolic syndrome x HSDN C0042963 Symptoms vomiting C1963068 Atrial flutter adverse event HSDN C0812426 Kidney problem C0748314 Renal insufficiency chronic etiology unknown UMLS C0426579 Anorexia symptom C0043251 Wounds and injuries HSDN C0036572 Convulsion C1847352 Polymicrogyria, bilateral frontoparietal MalaCards|HPO|UMLS C3641756 Have diarrhea C0014236 Endophthalmitis HSDN C4085210 Usual severity pain C0236736 Cocaine-related disorders HSDN C4085210 Usual severity pain C0014061 Tick-borne encephalitis HSDN C0016382 Cutaneous vascular engorgement C0033893 Tension headache HSDN C0015230 Exanthem C0268581 Holocarboxylase synthetase deficiency MalaCards|HPO|UMLS C0035232 Diaphragmatic paralysis C0037942 Spinal osteophytosis HSDN C0012833 Dizzy C0042594 Vestibular diseases UMLS C4085862 Bothered by nausea C1854107 Hyperaldosteronism, familial, type ii MalaCards C0018775 Hearing loss bilateral C0028326 Noonan syndrome HSDN C0004941 Behavioral symptoms C0432442 Chromosome 18p deletion syndrome MalaCards C3641755 Have constipation C3711749 Nonsyndromic holoprosencephaly MalaCards C0018681 Headache, cephalalgia C1512194 Gliomatosis cerebri type ii UMLS C0012833 Dizzy C2188188 Unreasonable fear being in open spaces, or crossing bridges HSDN C0039870 Leanness C0037369 Smoking HSDN C0020458 Hyperhydrosis C0017671 Glomus jugulare tumor HPO C1279888 Proteinuria of undiagnosed cause C0027868 Neuromuscular diseases HSDN C2024878 Cardiovascular surgery result: dyspnea C0524909 Hepatitis b, chronic HSDN C1963249 Tinnitus adverse event C0034067 Pulmonary emphysema HSDN C0020450 Hyperemesis gravidarum C0025202 Melanoma HSDN C1963093 Dizziness adverse event C0013502 Echinococcosis HSDN C4084767 Bothered by vomiting C4085311 Depression - recess HSDN C1557397 Adverse event associated with pain C0019087 Hemorrhagic disorders HSDN C0018991 Paralysis one side of body C1090821 Sepsis (invertebrate) HSDN C0344307 Analgesia C1855739 Indifference to pain, congenital, autosomal recessive HPO C0522224 Palsied C0032965 Pregnancy complications, infectious HSDN C4084766 Vomiting C0022408 Arthropathy HSDN C3641755 Have constipation C0004936 Mental disorders HSDN C1321898 Bloody stool C0025222 Melena UMLS C4085317 Diarrhea frequency C0403447 Chronic kidney insufficiency HSDN C4084802 Usual severity diarrhea C0004782 Basal ganglia diseases HSDN C1557397 Adverse event associated with pain C0024312 Lymphopenia HSDN C0039870 Leanness C0024141 Lupus erythematosus, systemic HSDN C0011991 Loose stools C0018852 Heavy chain disease HSDN C0036572 Convulsion C0266470 Cerebellar hypoplasia OrphaNet C4084775 Usual severity weight loss C0032226 Pleural diseases HSDN C1963087 Constipation adverse event C1997249 Neuralgia, pudendal MalaCards C1963065 Apnea adverse event C1881674 Medical device emits smoke HSDN C0023014 Developmental disorder language C0949628 Uniparental disomy HSDN C0032617 High urine output C2937421 Prostatic hyperplasia HSDN C3829611 Nausea frequency C0012979 Canine disease HSDN C0020538 Hbp C2931788 Atypical hemolytic uremic syndrome MalaCards C0010038 Corneal opacity disorder C1096100 Iridocorneal endothelial syndrome MalaCards C4084773 Bothered by weight gain C0018798 Congenital heart defects HSDN C1963091 Diarrhea adverse event C0206682 Follicular thyroid carcinoma HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0024636 Malocclusion HSDN C4084768 Usual severity vomiting C0018916 Hemangioma HSDN C1963087 Constipation adverse event C0033348 Language program HSDN C3539892 Pelvic pain in front C2350572 Illness behavior HSDN C0349588 Stature short C2748918 Otopalatodigital spectrum disorder HPO C0022346 Yellow skin C1836437 B-cell immunodeficiency, distal limb anomalies, and urogenital malformations MalaCards C0149793 Transient monocular blindness C1527406 Rhizomelic pseudopolyarthritis MalaCards C3539890 Pelvic pain causes awakening at night C0029400 Osteitis HSDN C0151603 Edema generalized C2873856 Essential cryoglobulinemia MalaCards C0009421 Comatose C0023522 Leukodystrophy, metachromatic OrphaNet|MalaCards C1963063 Anorexia adverse event C0008049 Chicken pox DiseaseOntology|MalaCards C0011570 Monopolar depression C3280371 Neurodegeneration with brain iron accumulation 4 MalaCards C4085548 Usual severity dizziness C0270639 Lateral sinus thrombosis HSDN C0042963 Symptoms vomiting C0269662 Hyperemesis gravidarum, starting before the end of the 22nd week of gestation, with metabolic disturbance, such as carbohydrate depletion UMLS C4085862 Bothered by nausea C0032371 Poliomyelitis HSDN C0023380 Lethargy C4084909 Depression subordinate domain HSDN C0242936 Center pain C0877149 Pain patellofemoral syndrome HSDN C1963281 Vomiting adverse event C0036875 Disorders of sex development HSDN C0036396 Sciatica C0460137 Push down or depress HSDN C0242670 Chronic vegetative state C0010399 Crying HSDN C2237041 Shox gene with short stature C3714896 Smith-mccort dysplasia 2 MalaCards C3898969 Have been vomiting C0006261 Bronchial diseases HSDN C3539891 Pelvic pain to the rear C0085096 Peripheral vascular diseases HSDN C4084784 Diarrhea C0020557 Hypertriglyceridemia HSDN C0018524 Hallucinate C0035078 Kidney failure HSDN C4085661 Usual severity nausea C0038358 Gastric ulcer HSDN C0234512 Prosopagnosia C0206616 Personal construct theory HSDN C4085210 Usual severity pain C0035436 Rheumatic fever HSDN C0267028 Lip pain C1300028 Disorder characterised by pain UMLS C0037316 Not enough sleeping C0020649 Hypotension HSDN C0043144 Wheeze C0264405 Asthma without status asthmaticus UMLS C0426579 Anorexia symptom C1000483 Genus anemia HSDN C2315100 Pediatric failure to thrive C0525043 Attachment disorder reactive HSDN C3887638 Failure to thrive in infant C0268151 Classical galactosemia OrphaNet|HPO|MalaCards C3494358 Characteristic, prodromal C0019360 Herpes zoster disease HSDN C0036659 Sensation disorder C0037313 Sleep HSDN C4084727 Cough frequency C0036202 Sarcoidosis OrphaNet|HSDN|HPO|MalaCards C2237041 Shox gene with short stature C1838652 Split-hand/foot malformation 3 MalaCards C0027796 Neuralgias C0037286 Skin neoplasms HSDN C0042571 Vertigo subjective C0018817 Atrial septal defects HSDN C0231341 Aging premature C1956346 Coronary artery disease HSDN C0749161 Supraclavicular swelling C0746345 Lymphoma nodular large cell UMLS C2237041 Shox gene with short stature C1860789 Leukemia, megakaryoblastic, of down syndrome HPO C0002622 Amnesias C1962976 Ventricular fibrillation adverse event HSDN C0033377 Caudal displacement C1862262 Bpes with ovarian failure HPO C0015469 Facial paralysis C0006277 Bronchitis HSDN C1527344 Dysphonia C0013423 Dystonia musculorum deformans HSDN C0030193 Sense of pain C0020514 Hyperprolactinemia HSDN C0234146 Absent reflex C0238027 Botulism, infantile OrphaNet|MalaCards C0024031 Back pain lower back C0003504 Aortic valve insufficiency HSDN C2919142 Short stature adverse event C0432221 Spondylometaphyseal dysplasia, 'corner fracture' type MalaCards C0162285 Edema eyelid C3553940 Peroxisome biogenesis disorder 5a (zellweger) MalaCards C2911645 Weight loss adverse event C0041324 Tuberculosis, osteoarticular HSDN C4084723 Constipation C0003811 Cardiac arrhythmia HSDN C4084726 Distress cough C2973787 Coxiella burnetii infection MalaCards C1963091 Diarrhea adverse event C0020649 Hypotension HSDN C0040264 Ear ringing sound C0042075 Urologic diseases HSDN C2096293 Ent surgical result ear vertigo C0702221 Tactual discrimination HSDN C1963180 Neck pain adverse event C0039483 Giant cell arteritis HSDN C3829611 Nausea frequency C0700327 Clinical findings relating to memory HSDN C0240735 Personality change C0859667 Cognitive or personality change of other type UMLS C2911645 Weight loss adverse event C0035579 Rickets HSDN C2984057 Have nausea C0007760 Cerebellar diseases HSDN C4085317 Diarrhea frequency C0042974 Von willebrand disease HSDN C1963087 Constipation adverse event C0038436 Post-traumatic stress disorder HSDN C0030552 Paralysis partial C2930798 Alexanders leukodystrophy MalaCards C1279888 Proteinuria of undiagnosed cause C0006818 Campylobacter infection HSDN C4084769 Vomiting frequency C2937287 Hematolysis HSDN C0026821 Cramp C1720189 Episodic ataxia MalaCards C0027497 Queasy C3272465 Ampulla of vater invasive papillary adenocarcinoma UMLS C0349588 Stature short C1856491 Gaucher disease, type iiia HPO C0033377 Caudal displacement C3469521 Fanconi anemia, complementation group a (disorder) MalaCards C0007758 Cerebellar ataxia C2750509 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 HPO|UMLS C0521503 Injection site burning C0521497 Injection site disorders UMLS C3146279 Coma C1535917 Nipah virus infection MalaCards C3541349 Syncope C0007930 Chagas cardiomyopathy HSDN C0004134 Dyssynergia C4014283 Cortical dysplasia, complex, with other brain malformations 6 MalaCards|UMLS C4084769 Vomiting frequency C0006736 Body stone HSDN C0151827 Pain eye C0024959 Maxillary sinusitis HSDN C0018524 Hallucinate C1555914 Psychologist - psychotherapy, group HSDN C1384666 Decreased hearing C2676244 Leukodystrophy, hypomyelinating, 6 MalaCards C0851578 Disorder sleep C0043253 Trauma blunt HSDN C0151786 Weakness muscle C0019625 Sinus histiocytosis HSDN C4085210 Usual severity pain C0556482 Protection sex HSDN C0085602 Polydypsia C3150796 Nephronophthisis 11 MalaCards|HPO|UMLS C0011991 Loose stools C0015927 Intrauterine fetal demise HSDN C0029163 Hemorrhage mouth C0030482 Paraepithymia HSDN C3539891 Pelvic pain to the rear C0020517 Hypersensitivity HSDN C4085211 Pain distress question C0042485 Venous insufficiency HSDN C0034933 Abnormal reflexes C0022904 Lacrimal apparatus diseases HSDN C3665347 Vision impaired C0268532 Deficiency of prolidase OrphaNet|HPO|MalaCards C1971624 Appetite absent C0038271 Stereotyped behavior HSDN C4085210 Usual severity pain C0029118 Opportunistic infections HSDN C4085210 Usual severity pain C0037397 Behavior social HSDN C0557874 Global developmental delay C3553517 Cornelia de lange syndrome 4 MalaCards C0003811 Cardiac rhythm disturbance C0205700 Asymmetric septal hypertrophy HPO C0557874 Global developmental delay C3149074 Seizures, benign familial neonatal, 1 HPO C2237041 Shox gene with short stature C1839736 Wilson-turner x-linked mental retardation syndrome HPO C4084726 Distress cough C0032963 Pregnancy complications, cardiovascular HSDN C2029884 Hearing loss by exam C0242952 Behavior infants HSDN C0036572 Convulsion C0265438 Chromosome 10 ring syndrome OrphaNet|MalaCards C0151908 Dry skin C1421143 Trh gene HPO C1557397 Adverse event associated with pain C0040409 Tongue diseases HSDN C0700078 Deep tendon reflex decrease C0008628 Chromosome deletion MalaCards C0013604 Edematous C0023493 Adult t-cell lymphoma/leukemia HSDN C2919142 Short stature adverse event C3536984 Vitamin d-resistant rickets, x-linked OrphaNet|HPO|MalaCards C4085548 Usual severity dizziness C0038454 Cerebrovascular accident HSDN C0023014 Developmental disorder language C0015630 Fantasies HSDN C4085210 Usual severity pain C0030297 Pancreatic neoplasm HSDN C0004604 Pain back C1552527 Clinic / center - developmental disabilities HSDN C0917816 Deficiency mental C0265202 Seckel syndrome OrphaNet|HPO|MalaCards C0015300 Ocular proptosis C1333989 Familial meningioma MalaCards C0018681 Headache, cephalalgia C2984572 Malaria pathway HSDN C1962972 Proteinuria adverse event C0037116 Silicosis HSDN C2029884 Hearing loss by exam C2020541 Strabismus HSDN C0022346 Yellow skin C0019212 Hepatorenal syndrome HSDN C0497406 Over weight C0021799 Interprofessional relations HSDN C0413252 Hypothermia due to exposure C0026850 Muscular dystrophy HSDN C3641756 Have diarrhea C0013504 Echinococcosis, hepatic HSDN C0007166 Cardiac output decreased C0242875 Ventricular septal rupture HSDN C0231528 Muscle pain generalized C0206586 Endolymphatic hydrops HSDN C0013362 Dysarthrias C1845028 Anemia, sideroblastic, and spinocerebellar ataxia HPO C2024893 Cardiovascular surgery result: fatigue C3489413 Lipomatosis, multiple HSDN C0030552 Paralysis partial C0024121 Lung neoplasms HSDN C4085211 Pain distress question C0023885 Liver abscess HSDN C3887638 Failure to thrive in infant C0008065 Childhood behavior HSDN C0036572 Convulsion C1848213 Periventricular heterotopia, x-linked HPO C4084775 Usual severity weight loss C0018099 Gout HSDN C4084724 Usual severity constipation C0002895 Anemia, sickle cell HSDN C4084727 Cough frequency C0162429 Malnutrition HSDN C3641755 Have constipation C0012147 Dientamoebiases HSDN C0013421 Dystonia C0027092 Myopia HSDN C0007859 Pain neck C1000483 Genus anemia HSDN C3539891 Pelvic pain to the rear C3495422 Finding relating to sexuality and sexual activity HSDN C4084774 Have weight loss C0867389 Chronic graft-versus-host disease MalaCards C3815497 Cough C0038436 Post-traumatic stress disorder HSDN C2984057 Have nausea C0016169 Pathologic fistula HSDN C4084768 Usual severity vomiting C0456892 Csf low pressure HSDN C0011206 Delirium acute C0314657 Genetic predisposition HSDN C0242936 Center pain C0014536 Epidural tumor HSDN C0011168 Disorder deglutition C0238462 Medullary carcinoma of thyroid OrphaNet C0009806 Constipate C0035412 Rhabdomyosarcoma HSDN C0149651 Clubbing C0455942 Clubbed nail; congenital UMLS C4084726 Distress cough C0152018 Esophageal carcinoma OrphaNet|MalaCards C0000737 Abdomen pain C0019294 Hernia, inguinal HSDN C0042928 Paralysis vocal cord C0025289 Meningitis HSDN C0037383 Sneeze C2240374 Eosinophil count raised HSDN C3641755 Have constipation C0220998 Hypothalamic hypothyroidism MalaCards C0042798 Vision dim C3276549 Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy MalaCards C0242936 Center pain C1547044 Kind of quantity - smell HSDN C0262384 Chest pain atypical C0026267 Mitral valve prolapse syndrome UMLS C2911645 Weight loss adverse event C0020517 Hypersensitivity HSDN C0004604 Pain back C0029463 Osteosarcoma HSDN C0234146 Absent reflex C1844873 Charcot-marie-tooth disease, x-linked recessive, 2 (disorder) OrphaNet C0000737 Abdomen pain C1333866 Grade 1 colon adenocarcinoma UMLS C1999266 Depression adverse event C0002875 Cooley's anemia OrphaNet|HPO C4084784 Diarrhea C0238198 Gastrointestinal stromal tumors HSDN C0242936 Center pain C0026705 Mucopolysaccharidosis ii HSDN C0015469 Facial paralysis C3554599 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 MalaCards C0030200 Intractable pain C0011849 Diabetes mellitus HSDN C1549543 Administration method - pain C0019554 Dislocate hip HSDN C0237326 Defecation pain C0151467 Addisonian crisis OrphaNet|MalaCards C0231218 Malaise generalized C3900102 Adult fibrolamellar carcinoma UMLS C4084768 Usual severity vomiting C1704436 Peripheral arterial diseases HSDN C0008031 Pain chest C0700327 Clinical findings relating to memory HSDN C1557397 Adverse event associated with pain C0003128 Anovulation HSDN C3539020 Pelvic pain decreasing in frequency C0019065 Hemorrhage intraperitoneal HSDN C0039070 Collapse fleeting C0011119 Decompression sickness HSDN C0002962 Angina C0043202 Wolff-parkinson-white syndrome HSDN C0042940 Disorder of voice C0032371 Poliomyelitis HSDN C0027498 Nausea vomiting C0020437 Hypercalcemia UMLS C2919142 Short stature adverse event C1414529 Fancc gene HPO C0042024 Urine incontinence C0949760 Personal autonomy HSDN C1384666 Decreased hearing C0796135 Renpenning syndrome 1 HPO C0018681 Headache, cephalalgia C0205768 Subependymal giant cell astrocytoma UMLS C4084776 Weight loss C0018995 Hemochromatosis HSDN C0030193 Sense of pain C0855007 Localized neuroepithelioma of bone UMLS C0349588 Stature short C0015624 Fanconi syndrome HPO C0030193 Sense of pain C0151814 Coronary occlusion HSDN C0020672 Body temperature decreased C0018944 Hematoma HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0024137 Lupus erythematosus, cutaneous HSDN C1961131 Cough adverse event C0015663 Fasting HSDN C0042571 Vertigo subjective C0456801 Ppv - peripheral positional vertigo UMLS C3665347 Vision impaired C2749685 Cystinosis, atypical nephropathic (disorder) HPO C2984058 Have pain C0036420 Localized scleroderma HSDN C3539890 Pelvic pain causes awakening at night C0004936 Mental disorders HSDN C0037771 Paraparesis spastic C1963137 Hydrocephalus adverse event HSDN C0026826 High muscle tone C0574080 Guanidinoacetate methyltransferase deficiency MalaCards|HPO C0004134 Dyssynergia C0003873 Rheumatoid arthritis HSDN C1963065 Apnea adverse event C0043253 Trauma blunt HSDN C4084802 Usual severity diarrhea C0037661 Somatostatinoma OrphaNet|MalaCards C0577572 Mass of musculoskeletal structure C0409785 Pigmented villonodular synovitis of wrist UMLS C0751188 Dural headache post puncture C0475525 Headache; spinal and epidural anesthesia-induced, during labor UMLS C3541349 Syncope C0034067 Pulmonary emphysema HSDN C0011991 Loose stools C0206172 Diabetic foot HSDN C4085317 Diarrhea frequency C0038013 Ankylosing spondylitis HSDN C4085211 Pain distress question C0006261 Bronchial diseases HSDN C2919142 Short stature adverse event C0376524 Branchio-oculo-facial syndrome OrphaNet|HPO|MalaCards C0042798 Vision dim C0007137 Squamous cell carcinoma HSDN C0233514 Behavior abnormal C0035436 Rheumatic fever MalaCards C1860844 Sparse, thin hair C2931008 Congenital disorder of glycosylation type 2a MalaCards|HPO C1279888 Proteinuria of undiagnosed cause C0004935 Animal ethology HSDN C0007166 Cardiac output decreased C0751803 Brain stem hemorrhage, post traumatic HSDN C4084727 Cough frequency C0035235 Respiratory syncytial virus infections MalaCards|HSDN C0557874 Global developmental delay C3281152 Chromosome 16q22 deletion syndrome MalaCards C4084802 Usual severity diarrhea C1849453 Rapadilino syndrome MalaCards|HPO C0018772 Deafness C1863371 Blepharophimosis, epicanthus inversus, and ptosis 3, formerly HPO C1963087 Constipation adverse event C1836522 Schindler disease, type ii MalaCards C4084727 Cough frequency C0717360 Disease lyme vaccine HSDN C0030552 Paralysis partial C1299262 Sarcoma - category (morphologic abnormality) HSDN C4084769 Vomiting frequency C0041312 Tuberculosis git nos DiseaseOntology|MalaCards C3539889 Pelvic pain increasing in severity C0010068 Coronary heart disease HSDN C0031911 Pigment deposition C0153422 Malig neop less curv stom unsp MalaCards C0011991 Loose stools C0037930 Spinal cord neoplasms HSDN C0018772 Deafness C3888081 L-2-hydroxyglutaric acidemia MalaCards C3641755 Have constipation C0001624 Adrenal gland neoplasms HSDN C0018524 Hallucinate C0024141 Lupus erythematosus, systemic HSDN C0026821 Cramp C0014038 Encephalitis HSDN C3539892 Pelvic pain in front C0004935 Animal ethology HSDN C4085317 Diarrhea frequency C1858592 Carney triad OrphaNet|MalaCards C1069915 Vertigo C0035302 Retinal artery occlusion HSDN C2242996 Tingling C0014804 Erythromelalgia HSDN C0039870 Leanness C0424318 Bullied HSDN C1549543 Administration method - pain C0021359 Infertility HSDN C0038002 Spleen enlargement C3809928 Alps3 MalaCards C2203646 Jaundice C0043395 Yellow fever DiseaseOntology|HSDN|OrphaNet|MalaCards C0162285 Edema eyelid C3714644 Thymus neoplasms OrphaNet|MalaCards C1963091 Diarrhea adverse event C1857449 Cutaneous photosensitivity and colitis, lethal MalaCards C0015469 Facial paralysis C0270952 Muscular dystrophy, oculopharyngeal MalaCards|HPO C0003467 Angst C1832903 Migraine, sporadic hemiplegic HPO C0002962 Angina C0005586 Bipolar disorder HSDN C0024031 Back pain lower back C0029134 Optic neuritis HSDN C1384666 Decreased hearing C0022738 Klippel-feil syndrome OrphaNet|HPO|MalaCards C0853986 Lymphocytes decreased C0023241 Legionnaires' disease MalaCards C0002965 Crescendo angina C3495422 Finding relating to sexuality and sexual activity HSDN C0392699 Dysaesthesia C0343068 Familial cold urticaria OrphaNet|HPO|MalaCards C0000737 Abdomen pain C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0041105 Jaw spasm C0079294 Epidermolysis bullosa dystrophica HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C0036271 Scalp dermatoses HSDN C0233514 Behavior abnormal C0878682 Ceruloplasmin deficiency OrphaNet|MalaCards C3539895 Pelvic pain occurs with bowel movement C2706915 Language:-:point in time:^patient:- HSDN C2984058 Have pain C0752308 Hypoxia-ischemia, brain HSDN C4084776 Weight loss C0040046 Thrombophlebitis HSDN C3641756 Have diarrhea C0020255 Hydrocephalus HSDN C1963184 Nystagmus adverse event C1859309 Syndactyly cenani lenz type MalaCards C0022346 Yellow skin C3151513 Mitochondrial dna depletion syndrome 3 (hepatocerebral type) MalaCards|HPO|UMLS C0028738 Nystagmus C0024408 Machado-joseph disease OrphaNet|MalaCards C2984058 Have pain C3538838 Nci ctep sdc rhabdomyosarcoma sub-category terminology HSDN C4085549 Dizziness C0006840 Candidiasis HSDN C0000727 Abdomen acute C1546949 Event consequence - death HSDN C4085211 Pain distress question C0019069 Hemophilia a HSDN C0013421 Dystonia C0086543 Cataract nos HSDN C0014591 Bleeding nose C0015503 Factor vii deficiency OrphaNet|HPO|MalaCards C0022346 Yellow skin C1546847 Entity name part type - family HSDN C3494358 Characteristic, prodromal C0525045 Mood disorders HSDN C0030552 Paralysis partial C0012979 Canine disease HSDN C0032617 High urine output C4085311 Depression - recess HSDN C4084774 Have weight loss C0026850 Muscular dystrophy HSDN C0042928 Paralysis vocal cord C1866552 Paragangliomas 2 (disorder) MalaCards|HPO C0023530 Leukopenia C3160738 Fanconi anemia, complementation group d2 MalaCards|HPO C4084773 Bothered by weight gain C0030920 Peptic ulcer HSDN C2919142 Short stature adverse event C0038015 Spondyloepiphyseal dysplasia OrphaNet C0233514 Behavior abnormal C0036421 Systemic scleroderma MalaCards C4084776 Weight loss C0334663 Histiocytic sarcoma HSDN C2237041 Shox gene with short stature C0023138 Laurence-moon syndrome OrphaNet|HPO|MalaCards C1961131 Cough adverse event C0013808 Electroconvulsive therapy HSDN C3463815 Feel fatigue C1333764 Gastric cronkhite canada polyposis MalaCards C4050613 Anxiety C0027873 Neuromyelitis optica MalaCards C0454644 Delayed language development C1853215 Autosomal recessive frontotemporal pachygyria OrphaNet|MalaCards C1549543 Administration method - pain C0001261 Actinomycosis HSDN C3539891 Pelvic pain to the rear C0001580 Adolescent behavior HSDN C0518090 Frequency of pain question C3160917 Bladder pain syndrome OrphaNet|MalaCards C3898969 Have been vomiting C0009946 Conversion disorder HSDN C1963091 Diarrhea adverse event C2931242 Familial waldmann's disease MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0015802 Femur fracture HSDN C1962972 Proteinuria adverse event C2827407 Infectious otitis media HSDN C0034642 Chest crepitation C1970472 Pulmonary alveolar proteinosis, acquired MalaCards C1971624 Appetite absent C0022661 Kidney failure, chronic HSDN C2024878 Cardiovascular surgery result: dyspnea C0027666 Neoplasms, radiation-induced HSDN C4084775 Usual severity weight loss C0151740 Intracranial hypertension HSDN C0002962 Angina C1961100 Erectile dysfunction adverse event HSDN C4085210 Usual severity pain C0032302 Mycoplasma pneumonia HSDN C0917816 Deficiency mental C1844696 Otopalatodigital syndrome, type ii OrphaNet|HPO|MalaCards C0040822 D tremors C0030567 Parkinson disease UMLS C0030554 Abnormal sensation C0021843 Intestinal obstruction HSDN C2242996 Tingling C0206655 Alveolar rhabdomyosarcoma HSDN C0741354 Axillary swelling C0741025 Chest problem UMLS C0018524 Hallucinate C0042138 Uterine neoplasms HSDN C0018772 Deafness C0038940 Surgical wound dehiscence HSDN C0011991 Loose stools C0039483 Giant cell arteritis HSDN C4084726 Distress cough C1306577 Dies patient HSDN C0234376 Tremor action C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|HPO|MalaCards C0030552 Paralysis partial C0037005 Shoulder dislocation HSDN C2984057 Have nausea C0021847 Intestinal pseudo-obstruction HSDN C0018681 Headache, cephalalgia C1336871 Meningioma of upper clivus UMLS C1860844 Sparse, thin hair C3542022 Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome MalaCards C0000737 Abdomen pain C0031142 Peritoneal diseases UMLS C4085210 Usual severity pain C0030186 Paget disease extramammary HSDN C4084766 Vomiting C0242383 Age related macular degeneration HSDN C0027796 Neuralgias C0009450 Disease caused by microorganism HSDN C3887873 Hearing loss C0795822 8 rec syndrome MalaCards C3898969 Have been vomiting C0002994 Angioedema HSDN C0007859 Pain neck C0020651 Hypotension, orthostatic HSDN C1000483 Genus anemia C0013366 Dyschondroplasia MalaCards|HPO C4084768 Usual severity vomiting C2675211 Episodic ataxia, type 6 (disorder) MalaCards C0270844 Convulsions tonic C0234533 Generalized seizures UMLS C0020903 Illusion C0004350 Authoritarianism HSDN C3887638 Failure to thrive in infant C0265201 De sanctis-cacchione syndrome MalaCards C0206160 Retic count elevated C0012979 Canine disease HSDN C0034124 Pupillary disorder C0238045 Carotid artery-cavernous sinus fistula HSDN C0231218 Malaise generalized C2981635 Stage iiia hilar cholangiocarcinoma UMLS C0040822 D tremors C0004096 Asthma HSDN C0018834 Brash C0343398 Cyclosporiases HSDN C3641756 Have diarrhea C0011880 Diabetic ketoacidosis HSDN C0010200 Cough symptom C0013926 Aeroembolism HSDN C0040822 D tremors C0007766 Intracranial aneurysm HSDN C0013404 Respiratory difficulty C1701938 Associated pulmonary arterial hypertension OrphaNet C0038002 Spleen enlargement C0268647 Lysinuric protein intolerance MalaCards|HPO C0018808 Murmur C4084909 Depression subordinate domain HSDN C1963093 Dizziness adverse event C0409959 Osteoarthritis, knee HSDN C0020673 Hypothermia (central) (local) C0021051 Immunologic deficiency syndromes HSDN C0030193 Sense of pain C0016079 Figural aftereffects HSDN C1557397 Adverse event associated with pain C1720830 Painful bladder syndrome OrphaNet|MalaCards C0028738 Nystagmus C0376329 New variant creutzfeldt-jakob disease MalaCards C1882272 Pain adverse event by ctcae anatomic descriptor C0034628 Radius fracture HSDN C0009398 Color vision defects C0003469 Anxiety disorders HSDN C0013604 Edematous C0018818 Ventricular septal defects HSDN C1963184 Nystagmus adverse event C3668943 Fatty acid hydroxylase-associated neurodegeneration MalaCards C4084766 Vomiting C0751753 Carbamoyl-phosphate synthase i deficiency disease HPO C1963180 Neck pain adverse event C1962986 Glaucoma adverse event HSDN C0812426 Kidney problem C0543793 Renal disease congenital UMLS C0011206 Delirium acute C2911643 Encounter due to family history of osteoporosis HSDN C2024893 Cardiovascular surgery result: fatigue C0043232 Simplification work HSDN C4084802 Usual severity diarrhea C2931884 Reticuloendotheliosis, familial, with eosinophilia HPO C1963281 Vomiting adverse event C0338078 Non-functioning pituitary gland neoplasm OrphaNet|MalaCards C2926613 Chest pain:finding:point in time:^patient:ordinal C0439840 Reflex motion descriptor HSDN C4085862 Bothered by nausea C0305062 Tetanus toxoids HSDN C1549543 Administration method - pain C0028738 Nystagmus HSDN C3641756 Have diarrhea C0041974 Urethral stricture HSDN C1557397 Adverse event associated with pain C0497552 Congenital neurologic anomalies HSDN C0018772 Deafness C0022541 Kearns-sayre syndrome OrphaNet|HPO|MalaCards C0151786 Weakness muscle C1857395 De toni-debre-fanconi syndrome HSDN C2315100 Pediatric failure to thrive C0268595 Glutaric aciduria, type 1 HPO C3463815 Feel fatigue C0007138 Carcinoma, transitional cell HSDN C1557397 Adverse event associated with pain C0043515 Zollinger-ellison syndrome HSDN C0023012 Delay language C0796094 Blepharophimosis syndrome ohdo type MalaCards C0002962 Angina C2711227 Steatohepatitis HSDN C0013395 Indigestion C0011881 Diabetic nephropathy HSDN C4084775 Usual severity weight loss C0039538 Teratoma HSDN C0042963 Symptoms vomiting C0033348 Language program HSDN C3898969 Have been vomiting C0009319 Colitis HSDN C0234428 Consciousness disturbance C0205898 Pineoblastoma MalaCards C3665347 Vision impaired C1864205 Macular degeneration, age-related, 1 MalaCards C1963077 Bone pain adverse event C2748503 Corneal dystrophy, subepithelial mucinous MalaCards C4084774 Have weight loss C0024232 Lymphatic metastasis HSDN C0020672 Body temperature decreased C0795623 Hepatitis a vaccine, inactivated HSDN C0042963 Symptoms vomiting C2911643 Encounter due to family history of osteoporosis HSDN C0152459 Striae C1836635 Loeys-dietz aortic aneurysm syndrome OrphaNet|HPO|MalaCards C0012833 Dizzy C0524910 Hepatitis c, chronic HSDN C3665492 Pigmentations C0346340 Adenoid cystic carcinoma of lacrimal gland MalaCards C1963170 Hypothermia adverse event C0023890 Liver cirrhosis HSDN C0003467 Angst C0393576 Chorea acanthocytosis syndrome OrphaNet|HPO|MalaCards C4084774 Have weight loss C1704272 Benign prostatic hyperplasia HSDN C0020580 Decreased sensation C0034931 Reflex sympathetic dystrophy HSDN C0013604 Edematous C0079731 B-cell lymphomas HSDN C4085210 Usual severity pain C0019554 Dislocate hip HSDN C3146279 Coma C0040558 Toxoplasmosis HSDN C0028738 Nystagmus C1856057 Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type OrphaNet|HPO C1963281 Vomiting adverse event C0020625 Hyponatremia HSDN C4085211 Pain distress question C0677607 Hashimoto disease HSDN C1961131 Cough adverse event C0022665 Kidney neoplasm HSDN C0085632 Listlessness C1969957 Creutzfeldt-jakob disease, heidenhain variant HPO C0030552 Paralysis partial C4039473 3-methylglutaconic aciduria type 5 MalaCards C0036572 Convulsion C2673535 Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive (disorder) HPO C1963091 Diarrhea adverse event C0030636 Pasteurella infection HSDN C3641756 Have diarrhea C0021308 Infarction HSDN C4084768 Usual severity vomiting C0020303 Hydropneumothorax HSDN C0002170 Alopecia disorders C0020758 Congenital ichthyosis MalaCards|HPO C4042891 Sleep wake disorders C0007771 Intracranial arteriosclerosis HSDN C0030552 Paralysis partial C0080179 Vertebra fracture HSDN C0518090 Frequency of pain question C0524801 Retinal neoplasms HSDN C0030554 Abnormal sensation C0271375 Cranial nerve palsy iv trochlear HSDN C0013362 Dysarthrias C1850599 Leigh syndrome due to mitochondrial complex iv deficiency HPO C0036572 Convulsion C3715049 Ceroid lipofuscinosis, neuronal, 13 UMLS C0009763 Conjunctiva inflammation C0221036 Acrodermatitis enteropathica OrphaNet|HPO C4084802 Usual severity diarrhea C0392607 Severe combined immunodeficiency due to adenosine deaminase deficiency MalaCards C1549543 Administration method - pain C0042485 Venous insufficiency HSDN C0026821 Cramp C0028768 Obsessive-compulsive disorder HSDN C0042963 Symptoms vomiting C0205788 Histiocytoid hemangioma HSDN C0036572 Convulsion C3897121 Recurrent childhood protoplasmic astrocytoma UMLS C0037771 Paraparesis spastic C0238288 Muscular dystrophy, facioscapulohumeral HSDN C0728710 Pupil constriction observed C1291564 Deficiency of aromatic-l-amino-acid decarboxylase MalaCards|HPO C3146279 Coma C0020649 Hypotension HSDN C0234471 Conduction aphasia C0085417 Epilepsy, complex partial HSDN C0242936 Center pain C0036095 Salivary gland neoplasms HSDN C0234132 Pyramidal sign C0037231 Sjogren-larsson syndrome OrphaNet|HPO|MalaCards C0917816 Deficiency mental C3150414 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 MalaCards|HPO C0020672 Body temperature decreased C0042035 Urination disorders HSDN C4084776 Weight loss C0016977 Gall bladder diseases HSDN C0020649 Blood pressure decreased C0036472 Scrub typhus OrphaNet|MalaCards C1963252 Tremor adverse event C0342257 Complications of diabetes mellitus HSDN C0746674 Muscle weakness generalized C1861753 Multiminicore disease, moderate, with hand involvement HPO C4084774 Have weight loss C0031099 Periodontitis HSDN C1963184 Nystagmus adverse event C1876175 Ataxia-telangiectasia variant MalaCards|HPO C2984058 Have pain C0037305 Neoplasm, skull HSDN C4085317 Diarrhea frequency C0014850 Esophageal atresia HSDN C1961131 Cough adverse event C0007772 Intracranial arteriovenous malformation HSDN C0424755 Fever symptoms C0149678 Epstein-barr virus infections HSDN C3829611 Nausea frequency C0524620 Metabolic syndrome x HSDN C0007758 Cerebellar ataxia C0342701 Transcobalamin ii deficiency MalaCards C0009676 Confusion state C0220981 Metabolic acidosis HSDN C4085862 Bothered by nausea C0032285 Pneumonia HSDN C0038002 Spleen enlargement C2675646 Niemann-pick disease, intermediate, protracted neurovisceral HPO C0003113 Anomia C0010678 Cysticercosis HSDN C4084769 Vomiting frequency C0017612 Glaucoma, open-angle HSDN C0002965 Crescendo angina C3539018 Nci ctep sdc melanoma sub-category terminology HSDN C0030193 Sense of pain C1548483 Leishmaniasis vaccine HSDN C0023380 Lethargy C0038220 Status epilepticus HSDN C4085661 Usual severity nausea C3810814 Myocardial infarction ecg assessment HSDN C1963281 Vomiting adverse event C0027809 Neurilemmoma HSDN C0008031 Pain chest C0282607 Vascular neoplasms HSDN C0015469 Facial paralysis C0238154 Epidural hematoma HSDN C0042928 Paralysis vocal cord C0302148 Blood clot HSDN C1963093 Dizziness adverse event C0024299 Lymphoma HSDN C2029884 Hearing loss by exam C0497327 Dementia HSDN C0030193 Sense of pain C0033595 Prostitution HSDN C0234518 Speech slurred C0007795 Diffuse cerebral sclerosis of schilder MalaCards C0011991 Loose stools C0878544 Cardiomyopathies HSDN C4084768 Usual severity vomiting C0023890 Liver cirrhosis HSDN C0033774 Skin pruritus C2981667 Stage iib distal bile duct cancer UMLS C1963065 Apnea adverse event C0036946 Sheep--diseases HSDN C4085210 Usual severity pain C3873472 Vulvovaginal gingival syndrome MalaCards C0011991 Loose stools C1848590 Vascular hyalinosis MalaCards C0036572 Convulsion C1516516 Chromosomal duplication HSDN C0917816 Deficiency mental C0041409 Turner syndrome, male MalaCards|HPO C2919142 Short stature adverse event C3150910 Rajab syndrome MalaCards C2911647 Weight gain adverse event C0305062 Tetanus toxoids HSDN C0018775 Hearing loss bilateral C0024904 Mastoiditis HSDN C4084776 Weight loss C1546747 Specimen source codes - polyps HSDN C0012833 Dizzy C3887678 Cpnet MalaCards C0022568 Inflammation corneal C2752147 Xeroderma pigmentosum, complementation group c HPO C0424755 Fever symptoms C0038186 Reflex, startle HSDN C4084769 Vomiting frequency C0033906 Psychological theories HSDN C3887638 Failure to thrive in infant C2751651 Chromosome 19q13.11 deletion syndrome OrphaNet|MalaCards C4084766 Vomiting C0027686 Pathologic neovascularization HSDN C0423813 Crack nail C1148551 X-linked dyskeratosis congenita MalaCards|HPO C0030193 Sense of pain C0008372 Intrahepatic cholestasis HSDN C1963093 Dizziness adverse event C1963064 Anxiety adverse event HSDN C0040264 Ear ringing sound C0005695 Bladder neoplasm HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013473 Eating disorders HSDN C3641756 Have diarrhea C0334633 Malignant lymphoma - lymphoplasmacytic MalaCards C4084773 Bothered by weight gain C0040435 Tooth diseases HSDN C0003862 Pain joint C0268425 Alstrom syndrome HSDN C0151786 Weakness muscle C0282207 Cronkhite-canada syndrome MalaCards C0020458 Hyperhydrosis C0221032 Familial generalized lipodystrophy OrphaNet|HPO|MalaCards C0026821 Cramp C0019681 Personality disorder histrionic HSDN C0398650 Idiopathic thrombocytopenia purpura C0019054 Hemolysis (disorder) HSDN C0030193 Sense of pain C0154731 Neuralgia, glossopharyngeal UMLS C0700078 Deep tendon reflex decrease C2750234 Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 MalaCards|HPO C1882272 Pain adverse event by ctcae anatomic descriptor C0848558 Hypospadias HSDN C3641756 Have diarrhea C0018939 Hematological disease HSDN C1963071 Back pain adverse event C0013595 Eczema HSDN C0013405 Dyspnea, paroxysmal C0017168 Gastroesophageal reflux disease HSDN C4085661 Usual severity nausea C0151744 Myocardial ischemia HSDN C0030193 Sense of pain C0038034 Beurmann disease HSDN C4085211 Pain distress question C0085605 Liver failure HSDN C2984057 Have nausea C0162651 Gastric outlet obstruction HSDN C2919142 Short stature adverse event C3542549 Spastic paraplegia 49, autosomal recessive MalaCards C0206160 Retic count elevated C0342907 Sitosterolemia MalaCards|HPO C1549543 Administration method - pain C0021845 Intestinal perforation HSDN C0013428 Painful urination C0014858 Esophageal motility disorders UMLS C0030486 Extremity paralysis, lower C0007286 Carpal tunnel syndrome HSDN C2911647 Weight gain adverse event C0221752 Rbc urine HSDN C0042571 Vertigo subjective C0037933 Spinal diseases HSDN C0036572 Convulsion C1332899 Cerebellar glioblastoma UMLS C4084727 Cough frequency C0003962 Ascites HSDN C0003550 Broca aphasia C0700327 Clinical findings relating to memory HSDN C0184567 Pain acute C0003467 Anxiety HSDN C3815497 Cough C2936664 Acquired hypogammaglobulinemia HSDN C0023012 Delay language C0265498 48, xxxy syndrome MalaCards C2919142 Short stature adverse event C2363814 Femur-fibula-ulna complex MalaCards C2024878 Cardiovascular surgery result: dyspnea C0035435 Rheumatism HSDN C0013395 Indigestion C0034885 Rectal neoplasms HSDN C4085317 Diarrhea frequency C0085859 Polyglandular type i autoimmune syndrome HPO C0013362 Dysarthrias C2931390 Anophthalmia, cleft lip-palate, facial anomalies, and cns anomalies and hypothalamic disorder MalaCards C4084767 Bothered by vomiting C0003811 Cardiac arrhythmia HSDN C3146279 Coma C0008073 Developmental disabilities HSDN C0232466 Feeding difficulty C2750220 Karak syndrome MalaCards|HPO C0149741 Nipple discharge C1335390 Microscopic breast papilloma UMLS C1263846 Attention deficit disorder with hyperactivity C2931811 Chromosome 18, trisomy 18p OrphaNet|MalaCards C1557397 Adverse event associated with pain C0035302 Retinal artery occlusion HSDN C1963252 Tremor adverse event C0014055 Encephalitis, epidemic HSDN C0041657 Consciousness loss C1962986 Glaucoma adverse event HSDN C1963180 Neck pain adverse event C0035243 Respiratory tract infections HSDN C4084769 Vomiting frequency C1850407 Navajo familial neurogenic arthropathy MalaCards|HPO C0577568 Mass of urinary system structure C1443972 Cyst of prostate UMLS C1962972 Proteinuria adverse event C1962963 Osteoporosis adverse event HSDN C4084774 Have weight loss C0017160 Gastroenteritis HSDN C1963063 Anorexia adverse event C0020517 Hypersensitivity HSDN C0022346 Yellow skin C0035921 Congenital rubella syndrome MalaCards C0028738 Nystagmus C3554182 Combined oxidative phosphorylation deficiency 15 MalaCards C1999266 Depression adverse event C1864846 Pigmented nodular adrenocortical disease, primary, 1 (disorder) HPO C4085210 Usual severity pain C0008626 Congenital chromosomal disease HSDN C4084769 Vomiting frequency C0220847 C hepatitis virus HSDN C1000483 Genus anemia C2931189 Neural crest tumor MalaCards C0242936 Center pain C0009405 Hereditary nonpolyposis colorectal neoplasms HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0006663 Calcinosis HSDN C0037771 Paraparesis spastic C0031485 Phenylketonurias HSDN C0004093 Asthenia C0031117 Peripheral neuropathy HSDN C4084784 Diarrhea C1527336 Sjogren's syndrome HSDN C0038506 Stutter C0007825 Behavior, ceremonial HSDN C0742324 Chest skin discoloration C0743783 Face skin discoloration UMLS C4084723 Constipation C0034065 Pulmonary embolism HSDN C0034124 Pupillary disorder C0019693 Hiv infections HSDN C0013604 Edematous C0027686 Pathologic neovascularization HSDN C0028738 Nystagmus C1836603 Foveal hypoplasia and anterior segment dysgenesis HPO C0917816 Deficiency mental C0342273 Transient neonatal diabetes mellitus MalaCards C1963281 Vomiting adverse event C2936779 Hydroxymethylbilane synthase deficiency MalaCards C4084784 Diarrhea C3714630 Infections, respirovirus HSDN C0020903 Illusion C0036363 Schizotypal personality disorder HSDN C0018681 Headache, cephalalgia C2930957 Hantavirosis MalaCards C0038868 Supranuclear palsy progressive C4041080 Neurocognitive disorders HSDN C0013144 Drowsy C2931833 Hyperinsulinemic hypoglycemia, familial, 2 MalaCards C0036659 Sensation disorder C0752299 Sleep wake transition disorders HSDN C1962972 Proteinuria adverse event C2749685 Cystinosis, atypical nephropathic (disorder) HPO C0151786 Weakness muscle C0085541 Epilepsy, frontal lobe HSDN C2024878 Cardiovascular surgery result: dyspnea C2186740 Reported urticaria HSDN C4085862 Bothered by nausea C0027121 Myositis HSDN C4085211 Pain distress question C0009319 Colitis HSDN C4085862 Bothered by nausea C0333355 Inflammatory disease of mucous membrane HSDN C1963137 Hydrocephalus adverse event C0391826 Lhermitte-duclos disease OrphaNet|HPO|MalaCards C0003079 Pupillary inequality C0003813 Arrhythmia sinus HSDN C0030193 Sense of pain C0919691 Anastomotic leaks HSDN C0009421 Comatose C0003493 Aortic diseases HSDN C0030554 Abnormal sensation C0021449 Abuse inhalant HSDN C0349588 Stature short C2717836 Steroid sulfatase deficiency disease MalaCards C0012833 Dizzy C0026896 Myasthenia gravis HSDN C0021359 Infertility C3151407 Globozoospermia, complete MalaCards C3887873 Hearing loss C0007789 Cerebral palsy HSDN C3829611 Nausea frequency C1299919 Enteric coccidiosis HSDN C1882272 Pain adverse event by ctcae anatomic descriptor C2073625 X-ray of chest: pleural effusion HSDN C0020615 Hypoglycemia nos C2748941 Glycogen storage disease, type ixa2 HPO C0727671 Red cross toothache drops C0018799 Heart diseases HSDN C3641756 Have diarrhea C3150354 Immunodeficiency, common variable, 2 MalaCards|HPO C0151908 Dry skin C0432267 Tricho thiodystrophy disorder MalaCards C4084725 Usual severity cough C0751552 Malignant neoplasm of thymus MalaCards C0349588 Stature short C2937419 Chromosome x pentasomy OrphaNet|MalaCards C4084726 Distress cough C0267830 Pyogenic liver abscess HSDN C0030193 Sense of pain C0011253 Delusions HSDN C0413252 Hypothermia due to exposure C0036118 Salmonella infections, animal HSDN C0011991 Loose stools C1833170 Wiskott-aldrich syndrome, autosomal dominant form UMLS C4084725 Usual severity cough C0032962 Pregnancy complications HSDN C4085862 Bothered by nausea C1962983 Cataract adverse event HSDN C0234369 Tremulous C0003467 Anxiety UMLS C0857305 Thrombocytopenia purpura C0010054 Coronary arteriosclerosis HSDN C0034150 Skin purpura C0002886 Anemia, macrocytic HSDN C2919142 Short stature adverse event C1858726 Congenital cataracts, facial dysmorphism, and neuropathy OrphaNet|HPO|MalaCards C2911645 Weight loss adverse event C0032749 Post-kala-azar dermal leishmaniasis MalaCards C2984058 Have pain C0001815 Primary myelofibrosis HSDN C0585542 Bppv - benign paroxysmal positional vertigo nystagmus C0001314 Acute disease UMLS C3146279 Coma C0042510 Ventricular fibrillation HSDN C3829611 Nausea frequency C0004030 Aspergillosis HSDN C1384666 Decreased hearing C1850626 Nathalie syndrome MalaCards C2237041 Shox gene with short stature C0398691 Hyperimmunoglobulinemia d MalaCards C2024878 Cardiovascular surgery result: dyspnea C0017601 Glaucomas HSDN C0010038 Corneal opacity disorder C1856476 Gaucher disease, type iiic MalaCards C0027796 Neuralgias C0022658 Kidney diseases HSDN C0042963 Symptoms vomiting C0031117 Peripheral neuropathy HSDN C2911645 Weight loss adverse event C0041325 Peritonitis, tuberculous HSDN C0424755 Fever symptoms C0027809 Neurilemmoma HSDN C0019079 Bloody sputum C2697310 Sarcoidosis, susceptibility to, 1 (finding) HSDN C0085602 Polydypsia C3838758 Familial hyperaldosteronism type 3 MalaCards C0027498 Nausea vomiting C0086774 Cold hemoglobinuria MalaCards C0016382 Cutaneous vascular engorgement C0025267 Multiple endocrine neoplasia type 1 HPO C0008031 Pain chest C0497327 Dementia HSDN C0007758 Cerebellar ataxia C1860518 Vasculopathy, retinal, with cerebral leukodystrophy HPO C4084776 Weight loss C0410422 Chronic multifocal osteomyelitis OrphaNet|MalaCards C1557397 Adverse event associated with pain C1879338 Bereavement, life event HSDN C0042571 Vertigo subjective C0013364 Dysautonomia, familial HSDN C1963170 Hypothermia adverse event C0026850 Muscular dystrophy HSDN C0917816 Deficiency mental C3150127 Bardet biedl syndrome 15 HPO C0030554 Abnormal sensation C0023786 Mucopolysaccharidosis i OrphaNet C0030193 Sense of pain C0007894 Cestode infections HSDN C0162298 Stiffness joints C2931370 Bilateral ulnar hypoplasia and mental retardation MalaCards C4085211 Pain distress question C0041330 Tuberculosis, spinal HSDN C0860603 Anxiety symptom C2674949 Chromosome 3q29 deletion syndrome MalaCards C0271215 Blindness legal C1836876 Pierson syndrome MalaCards|HPO C0036572 Convulsion C3888317 Sialidosis, type 2 OrphaNet C4085661 Usual severity nausea C1704212 Embolism embolus HSDN C0850758 Pain pelvic C1546847 Entity name part type - family HSDN C1963093 Dizziness adverse event C0023448 Lymphoid leukemia HSDN C4084726 Distress cough C0001486 Adenovirus infections HSDN C0518090 Frequency of pain question C0242994 Hantavirus infections HSDN C4084768 Usual severity vomiting C3812171 Bradycardia by ecg finding HSDN C2984057 Have nausea C0023890 Liver cirrhosis HSDN C0518090 Frequency of pain question C1258666 Myxoid cyst HSDN C3146279 Coma C0023524 Leukoencephalopathy, progressive multifocal HSDN C4049644 Depression C1858496 Advanced sleep-phase syndrome, familial HPO C0035078 Failure kidney C1857761 Alagille syndrome 2 MalaCards|HPO C0042025 Urinary incontinence stress C0018193 Granuloma, foreign-body HSDN C4084802 Usual severity diarrhea C0020557 Hypertriglyceridemia HSDN C3815497 Cough C0030305 Pancreatitis HSDN C4084802 Usual severity diarrhea C0155862 Streptococcal pneumonia HSDN C0030193 Sense of pain C0021432 Infratentorial neoplasms HSDN C0241137 Skin pallor C0034929 Reflex HSDN C3539890 Pelvic pain causes awakening at night C0034065 Pulmonary embolism HSDN C2984057 Have nausea C1522133 High cholesterol level HSDN C0037763 Spasm C1265748 Torsion HSDN C0041105 Jaw spasm C1999266 Depression adverse event HSDN C0018681 Headache, cephalalgia C0035042 Psychology and religion HSDN C2017298 Soft tissue swelling of right lower leg with discoloration C0037580 Soft tissue swelling UMLS C0037384 Snore C3553404 Auriculocondylar syndrome 2 MalaCards|UMLS C4084768 Usual severity vomiting C0021400 Influenza HSDN C0042024 Urine incontinence C0268164 Primary hyperoxaluria, type i HPO C0333243 Edema pitting C0268389 Amyloidosis, familial visceral MalaCards C4084767 Bothered by vomiting C0004935 Animal ethology HSDN C3887873 Hearing loss C0024530 Malaria HSDN C1963281 Vomiting adverse event C0086543 Cataract nos HSDN C4084788 Have dizziness C0024115 Lung diseases HSDN C0042798 Vision dim C3805604 Foveal hypoplasia 1 MalaCards C0027796 Neuralgias C0162429 Malnutrition HSDN C2032395 Pelvic pain on the left C0006118 Brain neoplasms HSDN C0085602 Polydypsia C0017979 Glycosuria HSDN C1999266 Depression adverse event C1834570 Myoclonic dystonia HPO C4085210 Usual severity pain C0017566 Gingival hyperplasia HSDN C4084784 Diarrhea C0013533 Echovirus infections HSDN C0271215 Blindness legal C0796016 Microphthalmia, syndromic 1 MalaCards|HPO C2024878 Cardiovascular surgery result: dyspnea C0030581 Parotid neoplasms HSDN C1838869 Proximal neurogenic muscle weakness C1839028 Mitochondrial myopathy with diabetes MalaCards C0030975 Disorders perception C0027831 Neurofibromatosis 1 HSDN C1557397 Adverse event associated with pain C0010678 Cysticercosis HSDN C1963093 Dizziness adverse event C0040053 Thrombosis HSDN C0851578 Disorder sleep C0026598 Movement perception HSDN C0033774 Skin pruritus C0033348 Language program HSDN C0030200 Intractable pain C0012243 Digestive system neoplasms HSDN C0232466 Feeding difficulty C3888244 Aicardi-goutieres syndrome 7 MalaCards C2911647 Weight gain adverse event C0850803 Anaphylaxis (non medication) HSDN C0497406 Over weight C0006277 Bronchitis HSDN C0240735 Personality change C4225325 Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 UMLS C0007758 Cerebellar ataxia C4014531 Epileptic encephalopathy, early infantile, 24 MalaCards C3539895 Pelvic pain occurs with bowel movement C0001418 Adenocarcinoma HSDN C1557397 Adverse event associated with pain C0723362 Sleep brand of diphenhydramine hydrochloride HSDN C0030552 Paralysis partial C0340803 Capillary malformation (disorder) HSDN C0040264 Ear ringing sound C0018801 Heart failure HSDN C0004941 Behavioral symptoms C0265210 Weaver syndrome MalaCards|HPO C4085549 Dizziness C0041234 Chagas disease HSDN C0013428 Painful urination C0033581 Prostatitis HSDN C1962957 Flushing adverse event C1866552 Paragangliomas 2 (disorder) MalaCards C0013911 Emaciate C1266119 Solitary fibrous tumor HSDN C1963184 Nystagmus adverse event C2673873 Bardet-biedl syndrome 13 HPO C0349588 Stature short C1263846 Attention deficit hyperactivity disorder MalaCards C0043094 Weight gain C1366535 Avp gene HSDN C4255480 Nausea:presence or threshold:point in time:^patient:ordinal C0013274 Patent ductus arteriosus HSDN C0010200 Cough symptom C0041327 Tuberculosis, pulmonary MalaCards C0518090 Frequency of pain question C1384665 Hfe gene HSDN C0013911 Emaciate C0079335 Aids feline HSDN C0020305 Fetal edema C0340834 Hennekam lymphangiectasia lymphedema syndrome MalaCards C0018681 Headache, cephalalgia C0013386 Dyskinesia, drug-induced HSDN C0917816 Deficiency mental C1412573 Asah1 gene HPO C0015672 Decreased energy C0854176 Malignant hepato-biliary neoplasm MalaCards C0030193 Sense of pain C0025060 Mediastinal cyst HSDN C1279888 Proteinuria of undiagnosed cause C0242383 Age related macular degeneration HSDN C1963067 Atrial fibrillation adverse event C2750069 Lipodystrophy, congenital generalized, type 4 MalaCards|HPO C3829611 Nausea frequency C0034065 Pulmonary embolism HSDN C0522224 Palsied C2936779 Hydroxymethylbilane synthase deficiency MalaCards C0241137 Skin pallor C0002895 Anemia, sickle cell HSDN C1963170 Hypothermia adverse event C1706377 Memory device component HSDN C4084766 Vomiting C0022593 Keratosis HSDN C0007758 Cerebellar ataxia C0034885 Rectal neoplasms HSDN C0030200 Intractable pain C0263859 Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome HSDN C4085548 Usual severity dizziness C0034065 Pulmonary embolism HSDN C0019079 Bloody sputum C0206629 Pulmonary blastoma OrphaNet|HSDN|UMLS|MalaCards C1961131 Cough adverse event C0859897 Cord dysfunction vocal HSDN C0242936 Center pain C0019151 Hepatic encephalopathy HSDN C1963137 Hydrocephalus adverse event C0268263 Multiple sulfatase deficiency disease OrphaNet|HPO|MalaCards C4084766 Vomiting C1864996 Enteric neuropathy, familial MalaCards C2984057 Have nausea C0022373 Disease, jejunal HSDN C0042963 Symptoms vomiting C0004238 Atrial fibrillation HSDN C4085548 Usual severity dizziness C1579931 Depressed - symptom HSDN C1549543 Administration method - pain C0162869 Aneurysm, ruptured HSDN C4085210 Usual severity pain C0005659 Bite sting HSDN C0018524 Hallucinate C0021563 Insanity defense HSDN C4085317 Diarrhea frequency C0678202 Granulomatous enteritis MalaCards C0018991 Paralysis one side of body C0001889 Akinetic mutism HSDN C0023012 Delay language C1832814 Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant MalaCards C2315100 Pediatric failure to thrive C0007193 Cardiomyopathy, dilated HSDN C1549543 Administration method - pain C0752347 Lewy body disease HSDN C0027498 Nausea vomiting C0020625 Hyponatremia UMLS C0018681 Headache, cephalalgia C0010267 Cranial nerve neoplasms HSDN C0022346 Yellow skin C1334543 Macrotrabecular hepatoblastoma UMLS C0851578 Disorder sleep C0026848 Myopathy HSDN C0026884 Muteness C0011142 Defense mechanism HSDN C0016199 Pain flank C0001624 Adrenal gland neoplasms HSDN C0340288 Angina stable C3541877 Dextrocardia by ecg finding HSDN C1384666 Decreased hearing C0001969 Alcoholic intoxication HSDN C2024878 Cardiovascular surgery result: dyspnea C0037929 Spinal cord injuries HSDN C0031911 Pigment deposition C1837873 Leber congenital amaurosis 9 (disorder) MalaCards C0036572 Convulsion C4024989 Hereditary nonpolyposis colorectal carcinoma MalaCards C0042964 Anticipatory vomiting C0037051 Behavior illness HSDN C0016199 Pain flank C0034067 Pulmonary emphysema HSDN C0006370 Bulimia C0011854 Diabetes mellitus, insulin-dependent HSDN C1962972 Proteinuria adverse event C0023467 Leukemia, myelocytic, acute HSDN C0042571 Vertigo subjective C0010823 Cytomegalovirus infections HSDN C0007758 Cerebellar ataxia C0270736 Essential tremor HSDN C2984057 Have nausea C3714514 Infection HSDN C3815497 Cough C0002170 Alopecia HSDN C4084766 Vomiting C0033348 Language program HSDN C2129327 Regurgitation of small amounts of fluid C0042842 Vitamin a deficiency MalaCards C0850758 Pain pelvic C0006663 Calcinosis HSDN C0013404 Respiratory difficulty C0030470 Paranasal sinus neoplasms HSDN C0009398 Color vision defects C0043207 Wolfram syndrome HSDN C0497406 Over weight C0001721 Emotional affect HSDN C0018784 Deafness sensorineural C1857344 Split-hand-foot malformation with sensorineural hearing loss HPO C0018524 Hallucinate C0268193 Nadh cytochrome b5 reductase deficiency HPO C2024893 Cardiovascular surgery result: fatigue C0272118 Warm autoimmune hemolytic anemia OrphaNet|MalaCards C1963064 Anxiety adverse event C1847987 Huntington disease-like 2 MalaCards|HPO C1963249 Tinnitus adverse event C0010068 Coronary heart disease HSDN C3274924 Have been coughing C0027663 Neoplasms, multiple primary HSDN C1963087 Constipation adverse event C0041107 Trisomy HSDN C0005904 Alteration in body temperature C0006845 Candidiasis, chronic mucocutaneous MalaCards|HPO C0085642 Asphyxia reticularis C0242666 Protein s deficiency HSDN C1579931 Depressed - symptom C1961835 Gaucher disease, type 1 MalaCards C3898969 Have been vomiting C0011849 Diabetes mellitus HSDN C0149793 Transient monocular blindness C1709838 Rare non-neoplastic disorder UMLS C4084769 Vomiting frequency C0018188 Granuloma HSDN C3539020 Pelvic pain decreasing in frequency C1394494 Cystocele, unspecified HSDN C0848203 Male pelvic pain C3887532 Ulceration HSDN C0231791 In toe C0265249 Mietens' syndrome MalaCards C0015230 Exanthem C0477520 Keratoderma in diseases ce UMLS C0013404 Respiratory difficulty C1963083 Cholecystitis adverse event HSDN C0010200 Cough symptom C1299262 Sarcoma - category (morphologic abnormality) HSDN C0042024 Urine incontinence C0041956 Ureteral obstruction HSDN C1860844 Sparse, thin hair C0406468 Loose anagen hair syndrome MalaCards C0011991 Loose stools C0376618 Endotoxemia HSDN C0018772 Deafness C0009475 Community mental health service HSDN C0010520 Skin cyanosis C0272088 Haemoglobinopathy with cyanosis, nos UMLS C0040264 Ear ringing sound C1136043 Acoustic schwannoma, bilateral HPO C0917816 Deficiency mental C1859566 Bardet-biedl syndrome 8 MalaCards|HPO C0027796 Neuralgias C0040038 Thromboembolism HSDN C0026838 Spasticity muscle C0039145 Syringomyelia and syringobulbia HSDN C0040034 Thrombocytopenia C2931875 Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells MalaCards C4084776 Weight loss C0263979 Myositis, purulent MalaCards C0011991 Loose stools C3714630 Infections, respirovirus HSDN C1557397 Adverse event associated with pain C0017563 Gingival diseases HSDN C4084767 Bothered by vomiting C0041956 Ureteral obstruction HSDN C4085210 Usual severity pain C0030790 Pelvis infection HSDN C4085549 Dizziness C0030297 Pancreatic neoplasm HSDN C3641756 Have diarrhea C0030521 Parathyroid neo