Disease Summary help help Associated Targets (1)Tclin1 Explore Associated Targets list Mondo Description Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene. Uniprot Description A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia. Mondo Term and Equivalent IDs MONDO:0008099: congenital stationary night blindness autosomal dominant 2 DOID:0110863: congenital stationary night blindness autosomal dominant 2open_in_newMESH:C566869: open_in_newOMIM:163500: NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2open_in_newUMLS:C1876182: open_in_new