{"orpha":217616,"name":"Fatty acid oxidation and ketogenesis disorder 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-217616/","orphanet_url":"https://www.orpha.net/en/disease/detail/217616","names":{"fr":{"name":"Anomalie de l'oxydation des acides gras et de la cétogenèse avec cardiomyopathie dilatée"},"de":{"name":"Fettsäureoxidationsstörung und Ketogenese-Defekt mit dilatativer Kardiomyopathie"},"es":{"name":"Trastorno de la cetogénesis y de la oxidación de los ácidos grasos con miocardiopatía dilatada"},"it":{"name":"Difetto dell'ossidazione degli acidi grassi e della chetogenesi con cardiomiopatia dilatativa"},"nl":{"name":"Vetzuuroxidatie- en ketogenesestoornis met gedilateerde cardiomyopathie"},"pt":{"name":"Doença da oxidação dos ácidos gordos e cetogénese com miocardiopatia dilatada"},"pl":{"name":"Zaburzenie oksydacji kwasów tłuszczowych i ketogenezy z kardiomiopatią rozstrzeniową"},"cs":{"name":"Dilatační kardiomyopatie s poruchou oxidace mastných kyselin a ketogenezí"},"uk":{"name":"Порушення окислення жирних кислот та кетогенезу з дилатаційною кардіоміопатією"},"zh":{"name":"脂肪酸氧化和生酮障碍伴扩张型心肌病"},"tr":{"name":"Dilate kardiyomiyopatili yağ asidi oksidasyonu ve ketogenez bozukluğu"}},"xrefs":[{"source":"MONDO","code":"16336","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680875","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":99901,"name":"Acyl-CoA dehydrogenase 9 deficiency","type":"Disease"},{"orpha":158,"name":"Systemic primary carnitine deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}