{"orpha":309115,"name":"Disorder of fatty acid oxidation and ketogenesis","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-309115/","orphanet_url":"https://www.orpha.net/en/disease/detail/309115","names":{"fr":{"name":"Trouble de l'oxydation des acides gras et de la cétogenèse"},"de":{"name":"Störung der Fettsäureoxidation und Ketogenese"},"es":{"name":"Trastorno de la oxidación de ácidos grasos y de la cetogénesis"},"it":{"name":"Difetto di ossidazione degli acidi grassi e della chetogenesi"},"nl":{"name":"Stoornis van vetzuuroxidatie en ketogenese"},"pt":{"name":"Alteração da oxidação do ácido goedo mitocondrial"},"pl":{"name":"Zaburzenia oksydacji kwasów tłuszczowych i ketogenezy"},"cs":{"name":"Poruchy oxidace mastných kyselin a ketogeneze"},"uk":{"name":"Порушення окислення жирних кислот і кетогенезу"},"zh":{"name":"脂肪酸氧化与生酮障碍"},"tr":{"name":"Yağ asidi oksidasyonu ve ketogenez bozukluğu"}},"xrefs":[{"source":"ICD-11","code":"5C52.01","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1861994414"},{"source":"MONDO","code":"0017713","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17713","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681071","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":79174,"name":"Disorder of fatty acid oxidation and ketone body metabolism","classifications":[150,156]}],"children":[{"orpha":20,"name":"3-hydroxy-3-methylglutaric aciduria","type":"Disease"},{"orpha":35701,"name":"3-hydroxy-3-methylglutaryl-CoA synthase deficiency","type":"Disease"},{"orpha":309127,"name":"3-hydroxyacyl-CoA dehydrogenase deficiency","type":"Clinical group"},{"orpha":309120,"name":"Acyl-CoA dehydrogenase deficiency","type":"Clinical group"},{"orpha":746,"name":"Mitochondrial trifunctional protein deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}