OBO ID: DOID:0110714
Term Name: congenital stationary night blindness 1G Search Ontology:
Synonyms:
  • congenital stationary night blindness type 1G
  • CSNB1G
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/22190596
References:
Ontology: Human Disease   (DOID:0110714)
OTHER congenital stationary night blindness 1G PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNAT1 Night blindness, congenital stationary, type 1G 616389
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None