{"orpha":183643,"name":"Genetic polyendocrinopathy","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-183643/","orphanet_url":"https://www.orpha.net/en/disease/detail/183643","names":{"fr":{"name":"Polyendocrinopathie génétique"},"de":{"name":"Polyendokrinopathie, genetisch bedingte"},"es":{"name":"Poliendocrinopatía genética"},"it":{"name":"Poliendocrinopatia genetica"},"nl":{"name":"Genetische polyendocrinopathie"},"pt":{"name":"Poliendocrinopatia genética"},"pl":{"name":"Poliendokrynopatia genetyczna"},"cs":{"name":"Dědičné polyendokrinopatie"},"uk":{"name":"Генетично обумовлена поліендокринопатія"},"zh":{"name":"遗传性多内分泌病"},"tr":{"name":"Genetik poliendokrinopati"}},"xrefs":[{"source":"UMLS","code":"C5680535","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":156638,"name":"Rare genetic endocrine disease","classifications":[156]}],"children":[{"orpha":3453,"name":"Autoimmune polyendocrinopathy type 1","type":"Disease"},{"orpha":1227,"name":"Bangstad syndrome","type":"Malformation syndrome"},{"orpha":37042,"name":"Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome","type":"Disease"},{"orpha":686495,"name":"MADD-related developmental delay-endocrine dysfunction-hypohemoglobinemia syndrome","type":"Disease"},{"orpha":100094,"name":"Multiple polyglandular tumor","type":"Category"},{"orpha":391487,"name":"STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome","type":"Disease"},{"orpha":445018,"name":"Syndromic autoimmune enteropathy due to LRBA deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}