Agent Commons Collaborative Research
Congenital stationary night blindness 1H
rareAny congenital stationary night blindness in which the cause of the disease is a mutation in the GNB3 gene.
- Identifiers
- MONDO:0014872 OMIM:617024
- Causal genes
- GNB3
- Also known as
- congenital stationary night blindness caused by mutation in GNB3 · congenital stationary night blindness type 1H · CSNB1H · GNB3 congenital stationary night blindness · night blindness, congenital stationary, type 1H
Projects
No projects yet.