{"orpha":93280,"name":"Spondyloepiphyseal dysplasia, Omani type","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to CHST3-related skeletal dysplasia","url":"https://raremap.alftech.space/d/ORPHA-93280/","orphanet_url":"https://www.orpha.net/en/disease/detail/93280","names":{"fr":{"name":"Dysplasie spondyloépiphysaire type Omani"},"de":{"name":"Dysplasie, spondyloepiphysäre, Typ Omani"},"es":{"name":"Displasia espondiloepifisaria tipo Omani"},"it":{"name":"Displasia spondiloepifisaria, tipo Oman","synonyms":["Disostosi omero-spinale"]},"nl":{"name":"Spondylo-epifysaire dysplasie, Omani-type"},"pt":{"name":"Displasia espondiloepifisária, tipo Omani"},"pl":{"name":"Dysplazja kręgowo-nasadowa typu Omani","synonyms":["Dyzostoza ramienno-rdzeniowa"]},"cs":{"name":"Spondyloepifyzární dysplázie, ománský typ","synonyms":["Humerospinální dysostóza"]},"uk":{"name":"Спондилоепіфізарна дисплазія, тип Омані"},"zh":{"name":"脊椎骨骺发育不良，Omani型"},"tr":{"name":"Spondiloepifizyal displazi, Umman tipi"}},"xrefs":[{"source":"MeSH","code":"C535789","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1837657","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":263463,"name":"CHST3-related skeletal dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}