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General Information
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| Term |
Oguchi disease-1 |
ID (Ontology) |
DOID:0110712 (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 or compound heterozygous mutation in the SAG gene on chromosome 2q37. |
| Also Known As |
"congenital stationary night blindness Oguchi type 1" ; "CSNBO1" |
| 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-1 | 4 | for disease ribbon | Oguchi disease-1 | 4 | model of | Oguchi disease-1 | 4 |
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Relationships