{"orpha":295217,"name":"OBSOLETE: Radio-ulnar synostosis, unilateral","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Radio-ulnar fusion, unilateral"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Isolated radio-ulnar synostosis","url":"https://raremap.alftech.space/d/ORPHA-295217/","orphanet_url":"https://www.orpha.net/en/disease/detail/295217","names":{"fr":{"name":"OBSOLETE : Synostose radio-ulnaire, unilatérale","synonyms":["OBSOLETE : Fusion radio-cubitale, unilatérale","OBSOLETE : Fusion radio-ulnaire, unilatérale","OBSOLETE : Synostose radio-cubitale, unilatérale"]},"de":{"name":"OBSOLET: Radioulnare Synostose, unilaterale","synonyms":["OBSOLET: Radioulnare Fusion, unilaterale"]},"es":{"name":"OBSOLETO: Sinostosis unilateral de radio-cúbito","synonyms":["OBSOLETO: Fusión unilateral de radio-cúbito"]},"it":{"name":"OBSOLETO: Sinostosi radio-ulnare, unilaterale","synonyms":["OBSOLETO: Fusione radio-ulnare, unilaterale"]},"nl":{"name":"OBSOLEET: Radio-ulnaire synostose, unilateraal","synonyms":["OBSOLEET: Radio-ulnaire fusie, unilateraal"]},"pt":{"name":"OBSOLETO: Sinostose radio-cubital, unilateral","synonyms":["OBSOLETO: Fusão radio-cubital, unilateral"]},"pl":{"name":"NIEAKTUALNE: Synostoza promieniowo-łokciowa, jednostronna","synonyms":["NIEAKTUALNE: Zrost promieniowo-łokciowy, jednostronny"]},"cs":{"name":"NEAKTUÁLNÍ: Unilaterální radio-ulnární synostóza","synonyms":["NEAKTUÁLNÍ: Unilaterální radio-ulnární fúze"]},"uk":{"name":"ЗАСТАРІЛО: Радіо-ульнарний синостоз, односторонній","synonyms":["ЗАСТАРІЛО: Радіоульнарне зрощення, одностороннє"]},"zh":{"name":"单侧桡尺关节融合","synonyms":["单侧桡尺骨骨性融合"]},"tr":{"name":"Radio-ulnar sinostoz, unilateral","synonyms":["Radio-ulnar füzyon, unilateral"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":3269,"name":"Isolated radio-ulnar synostosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}