{"orpha":717865,"name":"Rare congenital/chronic/intractable diarrhea 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-717865/","orphanet_url":"https://www.orpha.net/en/disease/detail/717865","names":{"fr":{"name":"Diarrhée congénitale/chronique/réfractaire rare avec maladie inflammatoire de l'intestin"},"de":{"name":"Seltene kongenitale chronische therapieresistente Diarrhoe mit entzündlicher Darmerkrankung"},"es":{"name":"Diarrea congénita rara crónica e intratable con enfermedad inflamatoria intestinal"},"it":{"name":"Diarrea congenita cronica non trattabile rara con malattia infiammatoria dell'intestino"},"nl":{"name":"Zeldzame congenitale/chronische/therapieresistente diarree met inflammatoire darmziekte"},"pt":{"name":"Congenital-chronic-intractable diarrhea with inflammatory bowel disease"},"pl":{"name":"Rare congenital/chronic/intractable diarrhea with inflammatory bowel disease"},"cs":{"name":"Rare congenital/chronic/intractable diarrhea 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":314373,"name":"Chronic infantile diarrhea due to guanylate cyclase 2C overactivity","type":"Disease"},{"orpha":714487,"name":"Congenital diarrhea-chronic gastrointestinal inflammation-ocular dysgenesis syndrome","type":"Disease"},{"orpha":92050,"name":"Congenital tufting enteropathy","type":"Disease"},{"orpha":2881,"name":"Cutaneous photosensitivity-lethal colitis syndrome","type":"Disease"},{"orpha":84064,"name":"Trichohepatoenteric syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}