infantile histiocytoid cardiomyopathy
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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infantile histiocytoid cardiomyopathy
Summary
infantile histiocytoid cardiomyopathy is a developmental defect during embryogenesis[1].
Key Facts
- infantile histiocytoid cardiomyopathy's instance of is recorded as developmental defect during embryogenesis[2].
- infantile histiocytoid cardiomyopathy's instance of is recorded as class of disease[3].
- infantile histiocytoid cardiomyopathy is a type of intrinsic cardiomyopathy[4].
- infantile histiocytoid cardiomyopathy is a type of mitochondrial disease with dilated cardiomyopathy[5].
- infantile histiocytoid cardiomyopathy is a type of genetic cardiac rhythm disease[6].
- infantile histiocytoid cardiomyopathy is a type of genetic disease[7].
- infantile histiocytoid cardiomyopathy is a type of monogenic disease[8].
- infantile histiocytoid cardiomyopathy's NCI Thesaurus ID is recorded as C45745[9].
- infantile histiocytoid cardiomyopathy's genetic association is recorded as CYTB[10].
- infantile histiocytoid cardiomyopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080198[11].
- infantile histiocytoid cardiomyopathy's exact match is recorded as http://identifiers.org/doid/DOID:0080198[12].
- infantile histiocytoid cardiomyopathy's exact match is recorded as http://purl.obolibrary.org/obo/HP_0005152[13].
- infantile histiocytoid cardiomyopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_137675[14].
- infantile histiocytoid cardiomyopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].