{"orpha":271835,"name":"Genetic digestive tract tumor","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-271835/","orphanet_url":"https://www.orpha.net/en/disease/detail/271835","names":{"fr":{"name":"Tumeur génétique du tube digestif"},"de":{"name":"Tumor des Verdauungstraktes, genetisch bedingter"},"es":{"name":"Tumor del tracto digestivo de origen genético"},"it":{"name":"Tumore genetico del tratto digestivo"},"nl":{"name":"Genetische spijsverteringskanaaltumor"},"pt":{"name":"Tumor do sistema digestivo, genético"},"pl":{"name":"Guz przewodu pokarmowego uwarunkowany genetycznie"},"cs":{"name":"Geneticky podmíněné nádory trávicího traktu"},"uk":{"name":"Генетично обумовлена пухлина травного тракту"},"zh":{"name":"遗传性消化道肿瘤"},"tr":{"name":"Genetik sindirim sistemi tümörü"}},"xrefs":[{"source":"MONDO","code":"17128","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680757","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":68336,"name":"Rare genetic tumor","classifications":[156]}],"children":[{"orpha":220460,"name":"Attenuated familial adenomatous polyposis","type":"Disease"},{"orpha":201,"name":"Cowden syndrome","type":"Clinical subtype"},{"orpha":733,"name":"Familial adenomatous polyposis","type":"Disease"},{"orpha":44890,"name":"Gastrointestinal stromal tumor","type":"Disease"},{"orpha":26106,"name":"Hereditary diffuse gastric cancer","type":"Disease"},{"orpha":443909,"name":"Hereditary nonpolyposis colon cancer","type":"Clinical group"},{"orpha":2869,"name":"Peutz-Jeghers syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}