{"orpha":217613,"name":"Mitochondrial disease with dilated cardiomyopathy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-217613/","orphanet_url":"https://www.orpha.net/en/disease/detail/217613","names":{"fr":{"name":"Maladie mitochondriale avec cardiomyopathie dilatée"},"de":{"name":"Mitochondriale Krankheit mit dilatativer Kardiomyopathie"},"es":{"name":"Enfermedad mitocondrial con miocardiopatía dilatada"},"it":{"name":"Malattia mitocondriale con cardiomiopatia dilatativa"},"nl":{"name":"Mitochondriale ziekte met gedilateerde cardiomyopathie"},"pt":{"name":"Doença mitocondrial com miocardiopatia dilatada"},"pl":{"name":"Choroba mitochondrialna z kardiomiopatią rozstrzeniową"},"cs":{"name":"Mitochondriální choroba s dilatační kardiomyopatií"},"uk":{"name":"Мітохондріальна хвороба з дилатаційною кардіоміопатією"},"zh":{"name":"线粒体疾病伴扩张型心肌病"},"tr":{"name":"Dilate kardiyomiyopatili mitokondriyal hastalık"}},"xrefs":[{"source":"MONDO","code":"16335","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680874","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97929,"name":"Rare cardiac disease"},"parents":[{"orpha":217607,"name":"Familial dilated cardiomyopathy","classifications":[146,156]},{"orpha":506225,"name":"Rare disorder potentially indicated for heart transplant","classifications":[233]}],"children":[{"orpha":111,"name":"Barth syndrome","type":"Disease"},{"orpha":137675,"name":"Histiocytoid cardiomyopathy","type":"Disease"},{"orpha":480,"name":"Kearns-Sayre syndrome","type":"Disease"},{"orpha":99718,"name":"Leber plus disease","type":"Disease"},{"orpha":550,"name":"MELAS","type":"Disease"},{"orpha":551,"name":"MERRF","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}