OBO ID: DOID:0110866
Term Name: congenital stationary night blindness 1H Search Ontology:
Synonyms:
  • congenital stationary night blindness type 1H
  • CSNB1H
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/27063057
References:
Ontology: Human Disease   (DOID:0110866)
OTHER congenital stationary night blindness 1H PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNB3 Night blindness, congenital stationary, type 1H 617024
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None