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| Term | dilated cardiomyopathy 1A | ID (Ontology) | DOID:0110425 (Human Disease) | |||||||||||||||||||||||||||
| Definition | A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21. | |||||||||||||||||||||||||||||
| Also Known As | "CDCD1" ; "dilated cardiomyopathy with conduction defect 1" ; "familial dilated cardiomyopathy with conduction defect due to LMNA mutation" | |||||||||||||||||||||||||||||
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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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autosomal genetic disease |__autosomal dominant disease__ intrinsic cardiomyopathy | |__dilated cardiomyopathy______| dilated cardiomyopathy 1A 14 rec. |
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| Is a |
autosomal dominant disease dilated cardiomyopathy |
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External Crossreferences & Linkouts
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MIM:115200 ORDO:300751 |
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