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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models