{"orpha":104004,"name":"Intestinal disease due to vitamin absorption anomaly","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-104004/","orphanet_url":"https://www.orpha.net/en/disease/detail/104004","names":{"fr":{"name":"Maladie intestinale due à une anomalie de l'absorption de vitamines"},"de":{"name":"Intestinale Krankheit durch Störung der Vitamin-Absorption"},"es":{"name":"Enfermedad intestinal por anomalía en la absorción de vitaminas"},"it":{"name":"Malattia intestinale da anomalia dell'assorbimento vitaminico"},"nl":{"name":"Darmziekte door vitamineabsorptieanomalie"},"pt":{"name":"Doença intestinal por anomalia na absorção de vitaminas"},"pl":{"name":"Choroba jelit z powodu wadliwej absorpcji witamin w jelitach"},"cs":{"name":"Střevní choroby způsobené anomálií absorpce vitaminů"},"uk":{"name":"Кишкові захворювання через аномалію всмоктування вітамінів"},"zh":{"name":"维生素吸收异常所致肠病"},"tr":{"name":"Vitamin absorpsiyon anomalisine bağlı bağırsak hastalığı"}},"xrefs":[{"source":"MONDO","code":"15179","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681746","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]},{"orpha":117569,"name":"Rare intestinal disease","classifications":[152]}],"children":[{"orpha":90045,"name":"Hereditary folate malabsorption","type":"Disease"},{"orpha":35858,"name":"Imerslund-Gräsbeck syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}