{"orpha":1534,"name":"OBSOLETE: Craniosynostosis-radial aplasia, Imaizumi type","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Imaizumi-Kuroki syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Syndromic craniosynostosis","url":"https://raremap.alftech.space/d/ORPHA-1534/","orphanet_url":"https://www.orpha.net/en/disease/detail/1534","names":{"fr":{"name":"OBSOLETE : Syndrome de craniosynostose-aplasie radiale, type Imaizumi","synonyms":["OBSOLETE : Syndrome d'Imaizumi-Kuroki"]},"de":{"name":"OBSOLET: Kraniosynostose mit Radiusaplasie Typ Imaizumi","synonyms":["OBSOLET: Imaizumi-Kuroki-Syndrom"]},"es":{"name":"OBSOLETO: Craneosinostosis-aplasia radial tipo Imaizumi","synonyms":["OBSOLETO: Síndrome de Imaizumi-Kuroki"]},"it":{"name":"OBSOLETO: Craniosinostosi - aplasia radiale, tipo Imaizumi","synonyms":["OBSOLETO: Sindrome di Imaizumi-Kuroki"]},"nl":{"name":"OBSOLEET: Craniosynostose-radiale aplasie, Imaizumi-type","synonyms":["OBSOLEET: Imaizumi-Kurokisyndroom"]},"pt":{"name":"OBSOLETO: Craniossinostose-aplasia radial, tipo Imaizumi","synonyms":["OBSOLETO: Síndrome Imaizumi-Kuroki"]},"pl":{"name":"NIEAKTUALNE: Kraniosynostoza-aplazja kosci promieniowej, typu Imaizumi","synonyms":["NIEAKTUALNE: Zespół Imaizumi i Kuroki"]},"cs":{"name":"NEAKTUÁLNÍ: Kraniosynostóza-radiální aplázie, typ Imaizumi","synonyms":["OBSOLETE: Imaizumi-Kuroki syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Краніосиностоз-аплазія променевої кістки, тип Імаїдзумі","synonyms":["ЗАСТАРІЛО: Синдром Імаїдзумі-Курокі"]},"zh":{"name":"弃用：Imaizumi型颅缝早闭-桡骨发育不良综合征","synonyms":["Imaizumi-Kuroki 综合征"]},"tr":{"name":"Eski adı: Kraniosinostoz-radyal aplazi, Imaizumi tipi","synonyms":["Imaizumi-Kuroki sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":139393,"name":"Syndromic craniosynostosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}