ORPHA:953
OBSOLETE: Acromesomelic dysplasia, Brahimi-Bacha type
inactive · referred to ORPHA:40Acromesomelic dysplasia, Maroteaux type
- 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 Acromesomelic dysplasia, Maroteaux type
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Acromesomelic dysplasia, Brahimi-Bacha type | |
| fr | OBSOLETE : Dysplasie acromésomélique type Brahimi-Bacha | |
| de | OBSOLET: Dysplasie, akromesomele, Typ Brahimi-Bacha | |
| es | OBSOLETO: Displasia acromesomélica tipo Brahimi Bacha | |
| it | OBSOLETO: Displasia acromesomelica, tipo Brahimi-Bacha | |
| nl | OBSOLEET: Acromesomele dysplasie, Brahimi-Bacha-type | |
| pt | OBSOLETO: Displasia acromesomélica, tipo Brahimi-Bacha | |
| pl | NIEAKTUALNE: Dysplazja akromezomeliczna typu Brahimi i Bacha | |
| cs | NEAKTUÁLNÍ: Akromesomelická dysplázie, typ Brahimi-Bacha | |
| uk | ЗАСТАРІЛО: Акромезотеліальна дисплазія, тип Брахімі-Бача | |
| zh | 废弃：肢端肢中发育不良，Brahimi-Bacha型 | |
| tr | Eski adı: Akromezomelik displazi, Brahimi-Bacha tipi |
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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/953
- This record as JSON: /data/d/953.json