{"orpha":93566,"name":"OBSOLETE: Pediatric Sjögren syndrome","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary Sjögren syndrome","url":"https://raremap.alftech.space/d/ORPHA-93566/","orphanet_url":"https://www.orpha.net/en/disease/detail/93566","names":{"fr":{"name":"OBSOLETE : Syndrome de Gougerot-Sjögren de l'enfant"},"de":{"name":"OBSOLET: Sjögren-Syndrom des Kindesalters"},"es":{"name":"OBSOLETO: Síndrome de Sjögren pediátrica"},"it":{"name":"OBSOLETO: Sindrome di Sjögren a esordio infantile"},"nl":{"name":"OBSOLEET: Pediatrisch Sjögrensyndroom"},"pt":{"name":"OBSOLETO: Síndrome Sjögren pediátrica"},"pl":{"name":"NIEAKTUALNE: Dzieciecy zespól Sjögrena"},"cs":{"name":"NEAKTUÁLNÍ: Pediatrický Sjögrenův syndrom"},"uk":{"name":"ЗАСТАРІЛО: Синдром Шегрена у дітей"},"zh":{"name":"弃用：小儿Sj÷gren综合征"},"tr":{"name":"Eski adı: Pediatrik Sjögren sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":289390,"name":"Primary Sjögren disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}