OBO ID: DOID:0110713 |
Term Name: | Oguchi disease-2 | Search Ontology: | |
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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
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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