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| Term | dilated cardiomyopathy 1LL | ID (Ontology) | DOID:0081157 (Human Disease) |
| Definition | A dilated cardiomyopathy that has_material_basis_in heterozygous mutation in the PRDM16 gene on chromosome 1p36. | ||
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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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autosomal genetic disease |__autosomal dominant disease__ intrinsic cardiomyopathy | |__dilated cardiomyopathy______| dilated cardiomyopathy 1LL 1 rec. |
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| Is a |
autosomal dominant disease dilated cardiomyopathy |
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| MIM:615373 | |||