{"orpha":3460,"name":"Torg-Winchester 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 Multicentric osteolysis-nodulosis-arthropathy spectrum","url":"https://raremap.alftech.space/d/ORPHA-3460/","orphanet_url":"https://www.orpha.net/en/disease/detail/3460","names":{"fr":{"name":"Syndrome de Torg-Winchester"},"de":{"name":"Torg-Winchester-Syndrom"},"es":{"name":"Síndrome de Torg-Winchester"},"it":{"name":"Sindrome Torg-Winchester"},"nl":{"name":"Syndroom van Torg-Winchester"},"pt":{"name":"Síndrome Torg-Winchester"},"pl":{"name":"Zespół Torga i Winchestera","synonyms":["Zespół Winchestera"]},"cs":{"name":"Winchesterův-Torgův syndrom","synonyms":["Winchesterův syndrom","Winchester-Torgův syndrom"]},"uk":{"name":"Синдром Торга-Вінчестера","synonyms":["Синдром Вінчестера"]},"zh":{"name":"Torg-Winchester综合征","synonyms":["Winchester综合征"]},"tr":{"name":"Torg-Winchester sendromu","synonyms":["Winchester sendromu"]}},"xrefs":[{"source":"UMLS","code":"C1850155","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10078901","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":371428,"name":"Multicentric osteolysis-nodulosis-arthropathy spectrum"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}