Search Ontology:
Human Disease
congenital stationary night blindness autosomal dominant 1
- Term ID
- DOID:0110862
- Synonyms
-
- CSNBAD1
- rhodopsin-related congenital stationary night blindness
- 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
- References
- Ontology
- Human Disease ( DOID:0110862 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations