{"orpha":104013,"name":"Metabolic disease with intestinal involvement","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-104013/","orphanet_url":"https://www.orpha.net/en/disease/detail/104013","names":{"fr":{"name":"Maladie métabolique avec atteinte intestinale"},"de":{"name":"Stoffwechselkrankheit mit Darmbeteiligung"},"es":{"name":"Enfermedad metabólica con afectación intestinal"},"it":{"name":"Malattia metabolica con coinvolgimento intestinale"},"nl":{"name":"Stofwisselingsziekte met betrokkenheid van darm"},"pt":{"name":"Doença metabólica com envolvimento intestinal"},"pl":{"name":"Choroba metaboliczna obejmująca jelita"},"cs":{"name":"Metabolické onemocnění s postižením střeva"},"uk":{"name":"Метаболічні захворювання з ураженням кишечника"},"zh":{"name":"肠受累代谢性疾病"},"tr":{"name":"Bağırsak tutulumu ile seyreden metabolik hastalık"}},"xrefs":[{"source":"MONDO","code":"15188","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681740","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19850","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":371188,"name":"Congenital disorder of glycosylation with intestinal involvement","type":"Category"},{"orpha":35698,"name":"Mitochondrial DNA depletion syndrome","type":"Category"},{"orpha":298,"name":"Mitochondrial neurogastrointestinal encephalomyopathy","type":"Disease"},{"orpha":699,"name":"Pearson syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}