Congenital stationary night blindness 1A

A congenital stationary night blindness caused by variants in the X-linked NYX gene.

Also known as: CSNB1A, NYX congenital stationary night blindness, NYX-related congenital stationary night blindness, congenital stationary night blindness caused by mutation in NYX, congenital stationary night blindness type 1A, hemeralopia-myopia, myopia-night blindness, night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive

46 clinical trials for this condition and its sub-types, 0 tagged with Congenital stationary night blindness 1A itself.