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congenital stationary night blindness 1A

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any congenital stationary night blindness in which the cause of the disease is a mutation in the NYX gene.
Uniprot Description A non-progressive retinal disorder characterized by impaired night vision. Congenital stationary night blindness type 1A is characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity.
Mondo Term and Equivalent IDs
MONDO:0010690:  congenital stationary night blindness 1A