{"orpha":1800,"name":"OBSOLETE: Craniofaciocervical osteoglyphic dysplasia","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Bazopoulou-Kyrkanidou syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary bone dysplasia with decreased bone density","url":"https://raremap.alftech.space/d/ORPHA-1800/","orphanet_url":"https://www.orpha.net/en/disease/detail/1800","names":{"fr":{"name":"OBSOLETE : Dysplasie cranio-cervico-faciale ostéoglyphique","synonyms":["OBSOLETE : Syndrome de Bazopoulou-Kyrkanidou"]},"de":{"name":"OBSOLET: Dysplasie, kranio-fazio-zerviko-osteoglyphische","synonyms":["OBSOLET: Bazopoulou-Kyrkanidou-Syndrom"]},"es":{"name":"OBSOLETO: Displasia craneofaciocervical osteoglífica","synonyms":["OBSOLETO: Síndrome de Bazopoulou-Kyrkanidou"]},"it":{"name":"OBSOLETO: Displasia cranio-cervico-facciale osteoglifica","synonyms":["OBSOLETO: Sindrome di Bazopoulou-Kyrkanidou"]},"nl":{"name":"OBSOLEET: Craniofaciocervicale osteoglyfische dysplasie","synonyms":["OBSOLEET: Bazopoulou-Kyrkanidousyndroom"]},"pt":{"name":"OBSOLETO: Displasia cranio-facio-cervical osteoglífica","synonyms":["OBSOLETO: Síndrome Bazopoulou-Kyrkanidou"]},"pl":{"name":"NIEAKTUALNE: Dysplazja czaszkowo-twarzowo-szyjna","synonyms":["NIEAKTUALNE: Zespół Bazopoulou i Kyrkanidou"]},"cs":{"name":"NEAKTUÁLNÍ: Kraniofaciocervikální osteoglyfická dysplázie","synonyms":["OBSOLETE: Bazopoulou-Kyrkanidou syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Краніофаціально-цервікальна остеогліфічна дисплазія","synonyms":["ЗАСТАРІЛО: Синдром Базопулу-Кирканіду"]},"zh":{"name":"弃用：颅-面-颈骨雕刻样发育不良","synonyms":["Bazopoulou-Kyrkanidou综合征"]},"tr":{"name":"Eski adı: Kraniyofasiyoservikal osteoglifik displazi","synonyms":["Bazopoulou-Kyrkanidou sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93446,"name":"Primary bone dysplasia with decreased bone density"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}