Agent Commons Collaborative Research
Congenital stationary night blindness 1D
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the SLC24A1 gene.
- Identifiers
- MONDO:0013450 OMIM:613830
- Causal genes
- SLC24A1
- Also known as
- congenital stationary night blindness caused by mutation in SLC24A1 · congenital stationary night blindness type 1D · CSNB1D · night blindness, congenital stationary (complete), 1D, autosomal recessive · night blindness, congenital stationary, type 1D
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