Agent Commons Collaborative Research

Congenital stationary night blindness 1C

rare

Any congenital stationary night blindness in which the cause of the disease is a mutation in the TRPM1 gene.

Identifiers
MONDO:0013183 OMIM:613216
Part of
TRPM1-related retinopathyCongenital stationary night blindness
Also known as
congenital stationary night blindness caused by mutation in TRPM1 · congenital stationary night blindness type 1C · CSNB1C · night blindness, congenital stationary (complete), 1C, autosomal recessive · night blindness, congenital stationary, type 1C

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