ORPHA:1800
OBSOLETE: Craniofaciocervical osteoglyphic dysplasia
inactive · referred to ORPHA:93446Primary bone dysplasia with decreased bone density
Synonyms: OBSOLETE: Bazopoulou-Kyrkanidou syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary bone dysplasia with decreased bone density
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Craniofaciocervical osteoglyphic dysplasia | OBSOLETE: Bazopoulou-Kyrkanidou syndrome |
| fr | OBSOLETE : Dysplasie cranio-cervico-faciale ostéoglyphique | OBSOLETE : Syndrome de Bazopoulou-Kyrkanidou |
| de | OBSOLET: Dysplasie, kranio-fazio-zerviko-osteoglyphische | OBSOLET: Bazopoulou-Kyrkanidou-Syndrom |
| es | OBSOLETO: Displasia craneofaciocervical osteoglífica | OBSOLETO: Síndrome de Bazopoulou-Kyrkanidou |
| it | OBSOLETO: Displasia cranio-cervico-facciale osteoglifica | OBSOLETO: Sindrome di Bazopoulou-Kyrkanidou |
| nl | OBSOLEET: Craniofaciocervicale osteoglyfische dysplasie | OBSOLEET: Bazopoulou-Kyrkanidousyndroom |
| pt | OBSOLETO: Displasia cranio-facio-cervical osteoglífica | OBSOLETO: Síndrome Bazopoulou-Kyrkanidou |
| pl | NIEAKTUALNE: Dysplazja czaszkowo-twarzowo-szyjna | NIEAKTUALNE: Zespół Bazopoulou i Kyrkanidou |
| cs | NEAKTUÁLNÍ: Kraniofaciocervikální osteoglyfická dysplázie | = en |
| uk | ЗАСТАРІЛО: Краніофаціально-цервікальна остеогліфічна дисплазія | ЗАСТАРІЛО: Синдром Базопулу-Кирканіду |
| zh | 弃用：颅-面-颈骨雕刻样发育不良 | Bazopoulou-Kyrkanidou综合征 |
| tr | Eski adı: Kraniyofasiyoservikal osteoglifik displazi | Bazopoulou-Kyrkanidou sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1800
- This record as JSON: /data/d/1800.json