{"orpha":225968,"name":"OBSOLETE: Inherited predisposition to essential thrombocythemia","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Familial essential thrombocythemia"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Essential thrombocythemia","url":"https://raremap.alftech.space/d/ORPHA-225968/","orphanet_url":"https://www.orpha.net/en/disease/detail/225968","names":{"fr":{"name":"OBSOLETE : Prédisposition héréditaire à la thrombocytémie essentielle","synonyms":["OBSOLETE : Thrombocytémie essentielle familiale"]},"de":{"name":"OBSOLET:Thrombozythämie, essenzielle, bei vererbter Prädisposition","synonyms":["OBSOLET: Thrombozythämie, essenzielle, familiäre Form"]},"es":{"name":"OBSOLETO: Predisposición hereditaria a la trombocitopenia esencial","synonyms":["OBSOLETO: Trombocitopenia esencial familiar"]},"it":{"name":"OBSOLETO: Trombocitemia essenziale familiare"},"nl":{"name":"OBSOLEET: Overgeërfde predispositie voor essentiële trombocythemie","synonyms":["OBSOLEET: Familiale essentiële trombocythemie"]},"pt":{"name":"OBSOLETO: Predisposição hereditária a trombocitopenia essencial"},"pl":{"name":"NIEAKTUALNE: Dziedziczna predyspozycja do nadplytkowosci samoistnej","synonyms":["NIEAKTUALNE: Rodzinna nadpłytkowość samoistna"]},"cs":{"name":"NEAKTUÁLNÍ: Zděděná predispozice k esenciální trombocytemii","synonyms":["NEAKTUÁLNÍ: Familiární esenciální trombocytémie"]},"uk":{"name":"ЗАСТАРІЛО: Спадкова схильність до есенціальної тромбоцитемії","synonyms":["ЗАСТАРІЛО: Сімейна есенціальна тромбоцитемія"]},"zh":{"name":"弃用：遗传性易换原发性血小板增多症易感","synonyms":["家族性原发性血小板增多症"]},"tr":{"name":"Eski adı: Esansiyel trombositemiye kalıtsal yatkınlık","synonyms":["Ailesel esansiyel trombositemi"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":3318,"name":"Essential thrombocythemia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}