{"orpha":717874,"name":"Rare inborn error of metabolism with inflammatory bowel disease","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-717874/","orphanet_url":"https://www.orpha.net/en/disease/detail/717874","names":{"fr":{"name":"Erreur innée rare du métabolisme avec maladie inflammatoire de l'intestin"},"de":{"name":"Seltene angeborene Stoffwechselstörung mit entzündlicher Darmerkrankung"},"es":{"name":"Error innato raro del metabolismo con enfermedad inflamatoria intestinal"},"it":{"name":"Errore congenito del metabolismo raro con malattia infiammatoria dell'intestino"},"nl":{"name":"Zeldzame aangeboren stofwisselingsziekte met inflammatoire darmziekte"},"pt":{"name":"Rare inborn error of metabolism with inflammatory bowel disease"},"pl":{"name":"Rare inborn error of metabolism with inflammatory bowel disease"},"cs":{"name":"Rare inborn error of metabolism with inflammatory bowel disease"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":717862,"name":"Rare disorder with inflammatory bowel disease","classifications":[152,156,233]}],"children":[{"orpha":79259,"name":"Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib","type":"Clinical subtype"},{"orpha":309025,"name":"Mevalonate kinase deficiency","type":"Disease"},{"orpha":298,"name":"Mitochondrial neurogastrointestinal encephalomyopathy","type":"Disease"},{"orpha":646,"name":"Niemann-Pick disease type C","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}