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| General Information | |||
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| Term | cone-rod dystrophy 13 | ID (Ontology) | DOID:0111016 (Human Disease) |
| Definition | A cone-rod dystrophy that has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.2. | ||
| Also Known As | "CORD13" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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monogenic disease_____ retinal degeneration__| cone-rod dystrophy |__cone-rod dystrophy 13 |
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| Parents/Children View Depth |
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| Is a | cone-rod dystrophy | ||
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External Crossreferences & Linkouts
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MESH:C567698 MIM:608194 |
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