OBO ID: DOID:0110862
Term Name: congenital stationary night blindness autosomal dominant 1 Search Ontology:
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)
OTHER congenital stationary night blindness autosomal dominant 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RHO Night blindness, congenital stationary, autosomal dominant 1 610445
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None