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| Term | retinal cone dystrophy 1 | ID (Ontology) | DOID:0081024 (Human Disease) |
| Definition | A cone dystrophy that is characterized as autosomal dominant form of diffuse cone degeneration. | ||
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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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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ retinal disease | |__cone dystrophy______________| retinal cone dystrophy 1 |
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Relationships
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| Is a |
autosomal dominant disease cone dystrophy |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:3196 MESH:C566719 MIM:180020 |
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