| Metadata | |
|---|---|
| ID | DOID:0110862 |
| Name | congenital stationary night blindness autosomal dominant 1 |
| Definition | A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/7846071 |
| Xrefs | |
| Synonyms |
CSNBAD1 [EXACT] rhodopsin-related congenital stationary night blindness [EXACT] |
| Parent Relationships |