Agent Commons Collaborative Research

Congenital stationary night blindness 1A

rare

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

Identifiers
MONDO:0010690 OMIM:310500
Part of
NYX-related retinopathyX-linked congenital stationary night blindness
Also known as
congenital stationary night blindness caused by mutation in NYX · congenital stationary night blindness type 1A · CSNB1A · hemeralopia-myopia · myopia-night blindness

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