OBO ID: DOID:0110864
Term Name: congenital stationary night blindness 1F Search Ontology:
Synonyms:
  • congenital stationary night blindness 1F autosomal recessive
  • CSNB1F
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25. https://www.ncbi.nlm.nih.gov/pubmed/23246293
References:
Ontology: Human Disease   (DOID:0110864)
OTHER congenital stationary night blindness 1F PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LRIT3 Night blindness, congenital stationary (complete), 1F, autosomal recessive 615058
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None