{"orpha":363306,"name":"Genetic 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-363306/","orphanet_url":"https://www.orpha.net/en/disease/detail/363306","names":{"fr":{"name":"Maladie intestinale due à une malabsorption des graisses d'origine génétique"},"de":{"name":"Genetisch bedingte intestinale Krankheit durch Fettmalabsorption"},"es":{"name":"Enfermedad intestinal de origen genético por malabsorción de grasa"},"it":{"name":"Malattia intestinale genetica da malassorbimento dei grassi"},"nl":{"name":"Genetische intestinale ziekte door malabsorptie van vet"},"pt":{"name":"Doença intestinal genética devido à má absorção de gordura"},"pl":{"name":"Genetyczna choroba jelit spowodowana złym wchłanianiem tłuszczy"},"cs":{"name":"Geneticky podmíněné nemoci střev způsobené malabsorbcí tuků"},"uk":{"name":"Генетично обумовлене захворювання кишечника, зумовлене мальабсорбцією жирів"},"zh":{"name":"脂肪吸收障碍所致遗传性肠道疾病"},"tr":{"name":"Yağ emilim bozukluğuna bağlı genetik bağırsak hastalığı"}},"xrefs":[{"source":"UMLS","code":"C5680981","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":165655,"name":"Genetic intestinal disease","classifications":[156]}],"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"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}