{"orpha":79183,"name":"Disorder of ketolysis","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-79183/","orphanet_url":"https://www.orpha.net/en/disease/detail/79183","names":{"fr":{"name":"Trouble de la cétolyse"},"de":{"name":"Ketokörper-Stoffwechselstörung"},"es":{"name":"Trastornos del metabolismo de los cuerpos cetónicos"},"it":{"name":"Difetto del metabolismo dei corpi chetonici"},"nl":{"name":"Stoornis van ketolyse"},"pt":{"name":"Doença de cetólise"},"pl":{"name":"Zaburzenie metabolizmu ciał ketonowych"},"cs":{"name":"Porucha ketolýzy"},"uk":{"name":"Порушення кетолізу"},"zh":{"name":"解酮作用异常"},"tr":{"name":"Ketoliz bozukluğu"}},"xrefs":[{"source":"ICD-11","code":"5C52.02","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1454722246"},{"source":"MONDO","code":"0019229","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19229","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681845","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":134,"name":"Beta-ketothiolase deficiency","type":"Disease"},{"orpha":832,"name":"Succinyl-CoA:3-oxoacid CoA transferase deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}