{"orpha":271847,"name":"Genetic neuroendocrine 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-271847/","orphanet_url":"https://www.orpha.net/en/disease/detail/271847","names":{"fr":{"name":"Tumeur neuroendocrine génétique"},"de":{"name":"Tumor, neuroendokriner, genetisch bedingter"},"es":{"name":"Tumor neuroendocrino genético"},"it":{"name":"Tumore endocrino genetico"},"nl":{"name":"Genetische neuro-endocriene tumor"},"pt":{"name":"Tumor endócrino, genético"},"pl":{"name":"Guz neuroendokrynny uwarunkowany genetycznie"},"cs":{"name":"Geneticky podmíněné endokrinní nádory"},"uk":{"name":"Генетично обумовлена нейроендокринна пухлина"},"zh":{"name":"遗传性神经内分泌肿瘤"},"tr":{"name":"Genetik nöroendokrin tümör"}},"xrefs":[{"source":"UMLS","code":"C5680760","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":68336,"name":"Rare genetic tumor","classifications":[156]}],"children":[{"orpha":178,"name":"Chordoma","type":"Disease"},{"orpha":324299,"name":"EPAS1-related polycythemia-pheochromocytoma/paraganglioma syndrome","type":"Disease"},{"orpha":404,"name":"Familial hyperaldosteronism type II","type":"Disease"},{"orpha":319494,"name":"Familial nonmedullary thyroid carcinoma","type":"Clinical group"},{"orpha":29072,"name":"Hereditary pheochromocytoma-paraganglioma","type":"Disease"},{"orpha":100094,"name":"Multiple polyglandular tumor","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}