Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Night Blindness, Congenital Stationary, Autosomal Dominant 2 PDE6B disease C1876182 GeneticVariation 0.9 disgenet
Night Blindness, Congenital Stationary, Autosomal Dominant 2 PDE6B disease C1876182 Biomarker 0.9 disgenet
Night Blindness, Congenital Stationary, Autosomal Dominant 2 PDE6B disease C1876182 CausalMutation 0.9 disgenet
click here to return to the previous page