OBO ID: DOID:0110865
Term Name: congenital stationary night blindness 1B Search Ontology:
Synonyms:
  • autosomal recessive complete congenital stationary night blindness
  • congenital stationary night blindness 1B autosomal recessive
  • CSNB1B
Definition: A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35. https://www.ncbi.nlm.nih.gov/pubmed/15781871
References:
Ontology: Human Disease   (DOID:0110865)
OTHER congenital stationary night blindness 1B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GRM6 Night blindness, congenital stationary (complete), 1B, autosomal recessive 257270
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None