{"orpha":1256,"name":"OBSOLETE: Blepharophimosis-radioulnar synostosis syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Jorgenson-Lenz syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Syndrome with synostosis or other joint formation defect","url":"https://raremap.alftech.space/d/ORPHA-1256/","orphanet_url":"https://www.orpha.net/en/disease/detail/1256","names":{"fr":{"name":"OBSOLETE : Syndrome de blépharophimosis-synostose radio-cubitale","synonyms":["OBSOLETE : Syndrome de Jorgenson-Lenz"]},"de":{"name":"OBSOLET: Blepharophimose-radioulnare Synostose-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de blefarofimosis-sinostosis radiocubital","synonyms":["OBSOLETO: Síndrome de Jorgenson-Lenz"]},"it":{"name":"OBSOLETO: Sindrome blefarofimosi-sinostosi radioulnare","synonyms":["OBSOLETO: Sindrome di Jorgenson-Lenz"]},"nl":{"name":"OBSOLEET: Blefarofimose - radio-ulnaire synostose-syndroom","synonyms":["OBSOLEET: Syndroom van Jorgenson-Lenz"]},"pt":{"name":"OBSOLETO: Síndrome de blefarofimose-sinostose radio-cubital"},"pl":{"name":"NIEAKTUALNE: Zwezenie szpary powiekowej - synostoza promieniowo-lokciowa","synonyms":["NIEAKTUALNE: Zespół Jorgensona i Lenza"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující blefarofimózu a radioulnární synostózu","synonyms":["NEAKTUÁLNÍ: Jorgensonův-Lenzův syndrom","NEAKTUÁLNÍ: Jorgenson-Lenzův syndrom"]},"uk":{"name":"Синдром блефарофімозно-радіоульнарного синостозу","synonyms":["ЗАСТАРІЛО: Синдром Йоргенсона-Ленца"]},"zh":{"name":"弃用：睑裂狭小-尺桡关节融合综合征","synonyms":["Jorgenson-Lenz综合征"]},"tr":{"name":"Eski adı: Blefarofimosis-radioulnar sinostozis sendromu","synonyms":["Jorgenson-Lenz sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93459,"name":"Syndrome with synostosis or other joint formation defect"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}