|OBO ID: DOID:0110713|
|Term Name:||Oguchi disease-2||Search Ontology:|
|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)|
|Ontology:||Human Disease (DOID:0110713)|
OTHER Oguchi disease-2 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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