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General Information
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| Term |
X-linked cone-rod dystrophy 1 |
ID (Ontology) |
DOID:0111008 (Human Disease) |
| Definition |
A cone-rod dystrophy that has_material_basis_in mutation in an alternative terminal exon 15 of the RPGR gene on chromosome Xp11. |
| Also Known As |
"COD1" ; "CORDX1" ; "X-linked cone dystrophy 1" |
| 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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X-linked cone-rod dystrophy 1 | 3 | for disease ribbon | X-linked cone-rod dystrophy 1 | 3 | model of | X-linked cone-rod dystrophy 1 | 3 |
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Relationships