SympGAN

Basic information of disease: C0302129

Disease name Achromatopsia 1
Disease ID (CUI) C0302129
Disease alias
Achromatopsia
Achromatopsia 1
Rod monochromacy
Rod monochromatism
Rod monochromatism (disorder)
Definition HPO2016_07_04: A condition where the retina contains no functional cone cells, so that in addition to the absence of color discrimination, vision in lights of normal intensity is difficult. [DDD: gblack
External links
Related genes of disease: C0302129
Predicted genes of disease: C0302129
Candidate genes predicted by knowledge inference algorithm,
HypER, based on SympGAN knowledge graph.