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General Information
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| Term |
Bothnia retinal dystrophy |
ID (Ontology) |
DOID:0050683 (Human Disease) |
| Definition |
A fundus dystrophy that is characterized by early onset of night blindness and decreased visual acuity that progresses to blindness in early adulthood, has_material_basis_in mutation in RLBP1 gene. |
| Also Known As |
"Vasterbotten dystrophy" |
| 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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Bothnia retinal dystrophy | 15 | for disease ribbon | Bothnia retinal dystrophy | 15 | model of | Bothnia retinal dystrophy | 15 |
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