{"orpha":165661,"name":"Genetic pancreatic 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-165661/","orphanet_url":"https://www.orpha.net/en/disease/detail/165661","names":{"fr":{"name":"Maladie pancréatique génétique"},"de":{"name":"Pankreaskrankheit, genetisch bedingte"},"es":{"name":"Enfermedad genética pancreática"},"it":{"name":"Malattia pancreatica di origine genetica"},"nl":{"name":"Genetische aandoening van pancreas","synonyms":["Genetische ziekte van alvleesklier"]},"pt":{"name":"Doença genética pancreática"},"pl":{"name":"Genetyczna choroba trzustki"},"cs":{"name":"Geneticky podmíněná onemocnění pankreatu"},"uk":{"name":"Генетично обумовлене захворювання підшлункової залози"},"zh":{"name":"遗传性胰腺病"},"tr":{"name":"Genetik pankreas hastalığı"}},"xrefs":[{"source":"MONDO","code":"15618","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680436","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97935,"name":"Rare gastroenterologic disease"},"parents":[{"orpha":165652,"name":"Rare genetic gastroenterological disease","classifications":[156]}],"children":[{"orpha":676,"name":"Autosomal dominant hereditary chronic pancreatitis","type":"Disease"},{"orpha":700124,"name":"Autosomal recessive hereditary chronic pancreatitis","type":"Disease"},{"orpha":586,"name":"Cystic fibrosis","type":"Disease"},{"orpha":309028,"name":"Disorder of lipid absorption and transport","type":"Category"},{"orpha":1333,"name":"Familial pancreatic carcinoma","type":"Disease"},{"orpha":456312,"name":"Infantile multisystem neurologic-endocrine-pancreatic disease","type":"Disease"},{"orpha":199337,"name":"Pancreatic insufficiency-anemia-hyperostosis syndrome","type":"Disease"},{"orpha":811,"name":"Shwachman-Diamond syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}