{"orpha":104005,"name":"Intestinal disease due to fat malabsorption","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-104005/","orphanet_url":"https://www.orpha.net/en/disease/detail/104005","names":{"fr":{"name":"Maladie intestinale due à une malabsorption des graisses"},"de":{"name":"Intestinale Krankheit durch Fettmalabsorption"},"es":{"name":"Enfermedad intestinal por una mala absorción de grasas"},"it":{"name":"Malattia intestinale da anomalia dell'assorbimento dei grassi"},"nl":{"name":"Darmziekte door vetmalabsorptie"},"pt":{"name":"Doença intestinal por má absorção de gordura"},"pl":{"name":"Choroba jelit z powodu złego wchłaniania tłuszczy"},"cs":{"name":"Střevní choroby způsobené malabsorpcí tuků"},"uk":{"name":"Захворювання кишечника через мальабсорбцію жирів"},"zh":{"name":"脂肪吸收障碍所致肠病"},"tr":{"name":"Yağ emilim bozukluğuna bağlı bağırsak hastalığı"}},"xrefs":[{"source":"MONDO","code":"15180","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681745","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19843","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":117569,"name":"Rare intestinal disease","classifications":[152]}],"children":[{"orpha":727915,"name":"APOB-related familial hypobetalipoproteinemia","type":"Disease"},{"orpha":14,"name":"Abetalipoproteinemia","type":"Disease"},{"orpha":37,"name":"Acrodermatitis enteropathica","type":"Disease"},{"orpha":71,"name":"Chylomicron retention disease","type":"Disease"},{"orpha":84065,"name":"Idiopathic malabsorption due to bile acid synthesis defects","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}