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congenital stationary night blindness autosomal dominant 2

Disease Summary
Associated Targets (1)
Tclin

1


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
MESH:C566869: 
UMLS:C1876182: