{"orpha":506216,"name":"Rare disorder potentially indicated for bowel transplant","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-506216/","orphanet_url":"https://www.orpha.net/en/disease/detail/506216","names":{"fr":{"name":"Maladie rare possiblement indiquée pour la transplantation intestinale"},"de":{"name":"Seltene Erkrankung zur potentiellen Darm-Transplantation indiziert"},"es":{"name":"Trastorno raro potencialmente indicado para trasplante de intestino"},"it":{"name":"Malattia rara con indicazione al trapianto intestinale"},"nl":{"name":"Zeldzame aandoening mogelijk geïndiceerd voor darmtransplantatie"},"pt":{"name":"Doença rara com potencial indicação para transplante intestinal"},"pl":{"name":"Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu jelita"},"cs":{"name":"Vzácná porucha indikovaná k transplantaci střeva"},"uk":{"name":"Рідкісне захворювання, яке може бути показанням для трансплантації кишківника"},"zh":{"name":"可能适用于肠道移植的罕见疾病"},"tr":{"name":"Bağırsak nakli için potansiyel olarak endike olan nadir hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681213","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":565779,"name":"Rare disorder potentially indicated for transplant or complication after transplantation"},"parents":[{"orpha":506207,"name":"Rare disorder potentially indicated for transplant","classifications":[233]}],"children":[{"orpha":96346,"name":"Anorectal malformation","type":"Category"},{"orpha":294422,"name":"Chronic intestinal failure","type":"Clinical syndrome"},{"orpha":104007,"name":"Congenital enteropathy involving intestinal mucosa development","type":"Category"},{"orpha":104003,"name":"Congenital intestinal transport defect","type":"Category"},{"orpha":313906,"name":"Congenital pancreatic cyst","type":"Morphological anomaly"},{"orpha":468635,"name":"Cryptogenic multifocal ulcerous stenosing enteritis","type":"Disease"},{"orpha":71274,"name":"Disseminated peritoneal leiomyomatosis","type":"Disease"},{"orpha":97945,"name":"Intestinal malformation","type":"Category"},{"orpha":104010,"name":"Intestinal polyposis syndrome","type":"Clinical group"},{"orpha":73014,"name":"Intractable diarrhea of infancy","type":"Category"},{"orpha":108971,"name":"Non-syndromic visceral malformation of the liver, biliary tract, pancreas or spleen","type":"Category"},{"orpha":168807,"name":"Primary malignant peritoneal tumor","type":"Category"},{"orpha":104009,"name":"Rare disease involving intestinal motility","type":"Category"},{"orpha":104012,"name":"Rare monogenic inflammatory bowel disease","type":"Category"},{"orpha":104011,"name":"Rare tumor of intestine","type":"Category"},{"orpha":104008,"name":"Short bowel syndrome","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}