inborn mitochondrial metabolism disorder histiocytoid cardiomyopathy https://rarediseases.info.nih.gov/diseases/9511/infantile-histiocytoid-cardiomyopathy https://www.malacards.org/card/cardiomyopathy_infantile_histiocytoid congenital cardiomyopathy cardiomyopathy, oncocytic UMLS:C1708371 isolated Cardiac lipidosis foamy myocardial transformation of infancy Orphanet:137675 cardiomyopathy, focal Lipid OMIM:500000 Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium. NCIT:C45745 cardiomyopathy, infantile xanthomatous histiocytoid cardiomyopathy Arachnocytosis of the myocardium focal lipid cardiomyopathy myocardial hamartoma DOID:0080198 GARD:0009511 infantile cardiomyopathy with histiocytoid change MONDO:0010771 MESH:C535584 infantile xanthomatous cardiomyopathy infantile histiocytoid cardiomyopathy oncocytic cardiomyopathy cardiomyopathy, infantile histiocytoid Purkinje cell hamartoma icd11.foundation:1870618141 MEDGEN:310844 familial dilated cardiomyopathy obsolete_histiocytoid cardiomyopathy