{"orpha":79665,"name":"Gardner syndrome","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Familial adenomatous polyposis","url":"https://raremap.alftech.space/d/ORPHA-79665/","orphanet_url":"https://www.orpha.net/en/disease/detail/79665","names":{"fr":{"name":"Syndrome de Gardner"},"de":{"name":"Gardner-Syndrom"},"es":{"name":"Síndrome de Gardner"},"it":{"name":"Sindrome di Gardner"},"nl":{"name":"Syndroom van Gardner"},"pt":{"name":"Síndrome Gardner"},"pl":{"name":"Zespół Gardnera"},"cs":{"name":"Gardnerův syndrom"},"uk":{"name":"Синдром Гарднера","definition":"Gardner syndrome is a severe form of familial adenomatous polyposis characterized by multiple adenomas in the colon and rectum associated with prominent extracolonic features including osteomas and multiple skin and soft tissue tumors."},"zh":{"name":"加德纳综合征"},"tr":{"name":"Gardner sendromu"}},"xrefs":[{"source":"ICD-11","code":"LD2D.3","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1428130769"},{"source":"MONDO","code":"0019336","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D005736","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0017097","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"6482","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10017727","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":733,"name":"Familial adenomatous polyposis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}