{"orpha":1271,"name":"Bowen syndrome","type":"Disease","group":"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 Zellweger syndrome","url":"https://raremap.alftech.space/d/ORPHA-1271/","orphanet_url":"https://www.orpha.net/en/disease/detail/1271","names":{"fr":{"name":"Syndrome de Bowen"},"de":{"name":"Bowen-Syndrom"},"es":{"name":"Síndrome de Bowen"},"it":{"name":"Sindrome di Bowen"},"nl":{"name":"Syndroom van Bowen"},"pt":{"name":"Síndrome Bowen"},"pl":{"name":"Zespół Bowena"},"cs":{"name":"Bowenův syndrom"},"uk":{"name":"Синдром Боуена"},"zh":{"name":"Bowen综合征"},"tr":{"name":"Bowen sendromu"}},"xrefs":[{"source":"OMIM","code":"211200","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1859404","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":912,"name":"Zellweger syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}