{"orpha":717877,"name":"Rare miscellaneous disease 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-717877/","orphanet_url":"https://www.orpha.net/en/disease/detail/717877","names":{"fr":{"name":"Trouble divers rare avec maladie inflammatoire de l'intestin"},"de":{"name":"Seltene sonstige Störungen mit entzündlicher Darmerkrankung"},"es":{"name":"Enfermedad miscelánea rara con enfermedad inflamatoria intestinal"},"it":{"name":"Malattia rara eterogenea con malattia infiammatoria dell'intestino"},"nl":{"name":"Zeldzame diverse ziekten met inflammatoire darmziekte"},"pt":{"name":"Miscellaneous disease with inflammatory bowel disease"},"pl":{"name":"Rare miscellaneous disease with inflammatory bowel disease"},"cs":{"name":"Rare miscellaneous disease 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":1775,"name":"Dyskeratosis congenita","type":"Disease"},{"orpha":3322,"name":"Hoyeraal-Hreidarsson syndrome","type":"Disease"},{"orpha":52417,"name":"MALT lymphoma","type":"Disease"},{"orpha":494433,"name":"MIRAGE syndrome","type":"Disease"},{"orpha":306498,"name":"PTEN hamartoma tumor syndrome","type":"Disease"},{"orpha":487796,"name":"Takenouchi-Kosaki syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}