Term Name:	infantile histiocytoid cardiomyopathy
Synonyms:
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.
Ontology:	Human Disease [DOID:0080198]   ( DOID:0080198 )