ORPHA:1789
OBSOLETE: Craniofacial dysostosis-arthrogryposis-progeroid appearance syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Van Biervliet-Hendrickx-van Ertbruggen 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Craniofacial dysostosis-arthrogryposis-progeroid appearance syndrome | OBSOLETE: Van Biervliet-Hendrickx-van Ertbruggen syndrome |
| fr | OBSOLETE : Syndrome de dysostose craniofaciale-arthrogrypose-aspect progéroïde | OBSOLETE : Syndrome de Van Biervliet-Hendrickx-van Ertbruggen |
| de | OBSOLET: Kraniofaziale Dysostose-Arthrogrypose-Progerie-artige Erscheinung-Syndrom | OBSOLET: Van Biervliet-Hendrickx-van Ertbruggen-Syndrom |
| es | OBSOLETO: Síndrome de disostosis craneofacial-artrogriposis-aspecto progeroide | OBSOLETO: Síndrome de Van Biervliet-Hendrickx-Van Ertbruggen |
| it | OBSOLETO: Sindrome disostosi craniofacciale-artrogriposi-aspetto progeroide | OBSOLETO: Sindrome di Van Biervliet-Hendrickx-Van Ertbruggen |
| nl | OBSOLEET: Craniofaciale dysostose - artrogrypose - progeroïde uiterlijk-syndroom | OBSOLEET: Syndroom van Van Biervliet-Hendrickx-van Ertbruggen |
| pt | OBSOLETO: Síndrome de disostose cranio-facial-artrogripose-hábito progeróide | OBSOLETO: Síndrome Van Biervliet-Hendrickx-van Ertbruggen |
| pl | NIEAKTUALNE: Dyzostoza czaszkowo-twarzowa - artrogrypoza - starczy wyglad | NIEAKTUALNE: Zespół Van Biervlieta, Hendrickx i van Ertbruggena |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující kraniofaciální dysostózu, artrogrypózu a progeroidní vzhled | = en |
| uk | ЗАСТАРІЛО: Синдром черепно-лицевого дизостозу-артрогрипозу-прогероїдної зовнішності | ЗАСТАРІЛО: Синдром Ван Біверліта-Хендрікса-ван Ертбрюггена |
| zh | 颅面骨发育不全-关节挛缩-早衰综合征 | Van Biervliet-Hendrickx-van Ertbruggen 综合征 |
| tr | Eski adı: Kraniofasiyal dizostoz-artrogripoz-progeroid görünüm sendromu | Van Biervliet-Hendrickx-van Ertbruggen 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/1789
- This record as JSON: /data/d/1789.json