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| Term | dilated cardiomyopathy 2F | ID (Ontology) | DOID:0081162 (Human Disease) |
| Definition | A dilated cardiomyopathy that is characterized by refractory ventricular arrhythmias and severe heart failure and that has_material_basis_in homozygous mutation in the BAG5 gene on chromosome 14q32. | ||
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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 recessive disease__ intrinsic cardiomyopathy | |__dilated cardiomyopathy_______| dilated cardiomyopathy 2F 1 rec. |
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| Is a |
autosomal recessive disease dilated cardiomyopathy |
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| MIM:619747 | |||