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General Information
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| Term |
Oguchi disease-2 |
ID (Ontology) |
DOID:0110713 (Human Disease) |
| 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. |
| Also Known As |
"congenital stationary night blindness Oguchi type 2" ; "CSNBO2" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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Oguchi disease-2 | 1 | for disease ribbon | Oguchi disease-2 | 1 | model of | Oguchi disease-2 | 1 |
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