{"orpha":77302,"name":"Oculo-oto-facial dysplasia","type":"Malformation syndrome","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 Burn-McKeown syndrome","url":"https://raremap.alftech.space/d/ORPHA-77302/","orphanet_url":"https://www.orpha.net/en/disease/detail/77302","names":{"fr":{"name":"Dysplasie oculo-oto-faciale"},"de":{"name":"Dysplasie, okulo-oto-faziale"},"es":{"name":"Displasia óculo-oto-facial"},"it":{"name":"Displasia oculo-oto-faciale"},"nl":{"name":"Oculo-oto-faciale dysplasie"},"pt":{"name":"Displasia oculo-oto-facial"},"pl":{"name":"Dysplazja oczno-uszno-twarzowa"},"cs":{"name":"Okulootofaciální dysplázie","synonyms":["Burnův-McKeownův syndrom","Burn-McKeownův syndrom"]},"uk":{"name":"Окулоотофаціальна дисплазія"},"zh":{"name":"眼-耳-面发育不良"},"tr":{"name":"Okülo-oto-yüz displazisi"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":1200,"name":"Burn-McKeown syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}