{"orpha":99872,"name":"OBSOLETE: Hashimoto-Pritzker syndrome","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Congenital Langerhans cell histiocytosis"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Langerhans cell histiocytosis","url":"https://raremap.alftech.space/d/ORPHA-99872/","orphanet_url":"https://www.orpha.net/en/disease/detail/99872","names":{"fr":{"name":"OBSOLETE : Syndrome de Hashimoto-Pritzker","synonyms":["OBSOLETE : Histiocytose langerhansienne congénitale"]},"de":{"name":"OBSOLET: Hashimoto-Pritzker-Syndrom","synonyms":["OBSOLET: Langerhans-Zell-Histiozytose, kongenitale"]},"es":{"name":"OBSOLETO: Síndrome de Hashimoto-Pritzker","synonyms":["OBSOLETO: Histiocitosis congénita de células de Langerhans"]},"it":{"name":"OBSOLETO: Sindrom di Hashimoto-Pritzker","synonyms":["OBSOLETO: Istiocitosi congenita a cellule di Langerhans"]},"nl":{"name":"OBSOLEET: Syndroom van Hashimoto-Pritzker","synonyms":["OBSOLEET: Congenitale Langerhanscelhistiocytose"]},"pt":{"name":"OBSOLETO: Síndrome Hashimoto-Pritzker"},"pl":{"name":"NIEAKTUALNE: Zespól Hashimoto i Pritzkera","synonyms":["NIEAKTUALNE: Wrodzona histiocytoza z komórek Langerhansa"]},"cs":{"name":"NEAKTUÁLNÍ: Hashimotova-Pritzkerova choroba","synonyms":["NEAKTUÁLNÍ: Vrozená Langerhansova histiocytóza X","NEAKTUÁLNÍ: Hashimoto-Pritzkerova choroba"]},"uk":{"name":"ЗАСТАРІЛО: Синдром Хашимото-Пріцкера","synonyms":["ЗАСТАРІЛО: Вроджений гістіоцитоз клітин Лангерганса"]},"zh":{"name":"弃用：Hashimoto-Pritzker综合征","synonyms":["先天性朗格汉斯细胞组织细胞增生症"]},"tr":{"name":"Eski adı: Hashimoto-Pritzker sendromu","synonyms":["Doğumsal Langerhans hücreli histiyositoz"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":389,"name":"Langerhans cell histiocytosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}