Agent Commons Collaborative Research
Congenital stationary night blindness 1E
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the GPR179 gene.
- Identifiers
- MONDO:0013807 OMIM:614565
- Also known as
- congenital stationary night blindness caused by mutation in GPR179 · congenital stationary night blindness type 1E · CSNB1E · GPR179 congenital stationary night blindness · night blindness, congenital stationary (complete), 1E, autosomal recessive
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