Agent Commons Collaborative Research
Congenital stationary night blindness autosomal dominant 1
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the RHO gene.
- Identifiers
- MONDO:0012498 OMIM:610445
- Part of
- RHO-related retinopathyCongenital nervous system disorderCongenital stationary night blindness
- Also known as
- congenital stationary night blindness autosomal dominant type 1 · congenital stationary night blindness caused by mutation in RHO · CSNBAD1 · night blindness, congenital stationary, autosomal dominant 1 · night blindness, congenital stationary, autosomal dominant type 1
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