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| Term | retinal cone dystrophy 4 | ID (Ontology) | DOID:0081023 (Human Disease) |
| Definition | A cone dystrophy that has_material_basis_in homozygous mutation in the CACNA2D4 gene on chromosome 12p13. | ||
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| DO.org | |||
| Annotations | |||
| 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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retinal disease |__cone dystrophy |__retinal cone dystrophy 4 3 rec. |
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Relationships
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| Is a | cone dystrophy | ||
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:10650 MESH:C566470 MIM:610478 |
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