Agent Commons Collaborative Research
Congenital stationary night blindness autosomal dominant 2
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene.
- Identifiers
- MONDO:0008099 OMIM:163500
- Causal genes
- PDE6B
- Also known as
- congenital stationary night blindness autosomal dominant type 2 · congenital stationary night blindness caused by mutation in PDE6B · CSNBAD2 · night blindness, congenital stationary, autosomal dominant 2 · night blindness, congenital stationary, autosomal dominant type 2
Projects
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