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| Term | infantile histiocytoid cardiomyopathy | ID (Ontology) | DOID:0080198 (Human Disease) |
| Definition | An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b. | ||
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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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cardiomyopathy |__intrinsic cardiomyopathy__ genetic disease | |__monogenic disease_________| infantile histiocytoid cardiomyopathy |
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Relationships
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| Is a |
monogenic disease intrinsic cardiomyopathy |
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External Crossreferences & Linkouts
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GARD:9511 MIM:500000 |
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