OBO ID: DOID:0110713
Term Name: Oguchi disease-2 Search Ontology:
Synonyms:
  • congenital stationary night blindness Oguchi type 2
  • CSNBO2
Definition: A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_material_basis_in homozygous mutation in the GRK1 gene on chromosome 13q34. (2)
References:
Ontology: Human Disease   (DOID:0110713)
OTHER Oguchi disease-2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GRK1 Oguchi disease-2 613411
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None