OBO ID: DOID:0110868
Term Name: congenital stationary night blindness 1D Search Ontology:
Synonyms:
  • congenital stationary night blindness 1D autosomal recessive
  • CSNB1D
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SLC24A1 gene on chromosome 15q22. https://www.ncbi.nlm.nih.gov/pubmed/20850105
References:
Ontology: Human Disease   (DOID:0110868)
OTHER congenital stationary night blindness 1D PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC24A1 Night blindness, congenital stationary (complete), 1D, autosomal recessive 613830
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None