OBO ID: DOID:0110715
Term Name: congenital stationary night blindness autosomal dominant 3 Search Ontology:
Synonyms:
  • CSNBAD3
  • Nougaret type congenital stationary night blindness
Definition: A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/8673138
References:
Ontology: Human Disease   (DOID:0110715)
OTHER congenital stationary night blindness autosomal dominant 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNAT1 Night blindness, congenital stationary, autosomal dominant 3 610444
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None