{"orpha":438072,"name":"Disorder of keton body transport","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-438072/","orphanet_url":"https://www.orpha.net/en/disease/detail/438072","names":{"fr":{"name":"Trouble du transport des corps cétoniques"},"de":{"name":"Ketonkörper-Transport-Störung"},"es":{"name":"Trastorno del transporte de cuerpos cetónicos"},"it":{"name":"Disturbo del trasporto dei corpi chetonici"},"nl":{"name":"Stoornis van transport van ketonlichamen"},"pt":{"name":"Transtonos do transporte do corpo de cetona"},"pl":{"name":"Zaburzenie transportu ciał ketonowych"},"cs":{"name":"Porucha transportu ketolátek"},"uk":{"name":"Порушення транспорту кетонових тіл"},"zh":{"name":"酮体运输障碍"},"tr":{"name":"Keton cisimciği taşıma bozukluğu"}},"xrefs":[{"source":"MONDO","code":"18579","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681184","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":438075,"name":"Ketoacidosis due to monocarboxylate transporter-1 deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}