{"orpha":374,"name":"Goldenhar syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Facioauriculovertebral sequence"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Oculo-auriculo-vertebral spectrum","url":"https://raremap.alftech.space/d/ORPHA-374/","orphanet_url":"https://www.orpha.net/en/disease/detail/374","names":{"fr":{"name":"Syndrome de Goldenhar","synonyms":["Séquence facioauriculovertébrale"]},"de":{"name":"Goldenhar-Syndrom"},"es":{"name":"Síndrome de Goldenhar","synonyms":["Secuencia facio-aurículo-vertebral"]},"it":{"name":"Sindrome di Goldenhar","synonyms":["Displasia OAV","Displasia facio-auricolo-vertebrale","Displasia oculo-auricolo-vertebrale","Microsomia craniofacciale","OAVS","Sindrome oculo-auricolo-vertebrale","Spettro allargato della microsomia emifacciale","Spettro oculo-auricolo-vertebrale"]},"nl":{"name":"Syndroom van Goldenhar","synonyms":["Facioauriculovertebrale sequentie"]},"pt":{"name":"Síndrome Goldenhar","synonyms":["Displasia óculo-auriculo-vertebral","Microssomia hemifacial"]},"pl":{"name":"Zespół Goldenhara","synonyms":["Dysplazja OAV","Dysplazja oczno-uszno-kręgowa/kręgosłupowa","Dysplazja twarzowo-uszno-kręgowa/kręgosłupowa","OAVS","Rozszerzone spektrum mikrosomii połowy twarzy","Spektrum oczno-uszno-kręgowe/kręgosłupowe","Zespół oczno-uszno-kręgowy/kręgosłupowy"]},"cs":{"name":"Goldenharův syndrom","synonyms":["Facioaurikulovertebrální sekvence","OAV","OAVS","Okuloaurikulovertebrální dysplázie","Okuloaurikulovertebrální syndrom"]},"uk":{"name":"Синдром Гольденхара","synonyms":["Фаціоаурикуловертебральна послідовність"]},"zh":{"name":"Goldenhar综合征","synonyms":["面-耳-脊椎序列征"]},"tr":{"name":"Goldenhar sendromu","synonyms":["Fasiyoaurikulovertebral dizi"]}},"xrefs":[{"source":"MeSH","code":"D006053","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":141132,"name":"Craniofacial microsomia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}