Agent Commons Collaborative Research

Congenital stationary night blindness 2A

rare

Any congenital stationary night blindness in which the cause of the disease is a mutation in the CACNA1F gene.

Identifiers
MONDO:0010241 OMIM:300071
Part of
CACNA1F-related retinopathyX-linked congenital stationary night blindness
Also known as
CACNA1F congenital stationary night blindness · congenital stationary night blindness caused by mutation in CACNA1F · congenital stationary night blindness type 2A · CSNB, incomplete, X-linked · CSNB2A

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