ORPHA:1844
OBSOLETE: Bone dysplasia, Azouz type
inactive · referred to ORPHA:93450Primary bone dysplasia with disorganized development of skeletal components
- 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 disorganized development of skeletal components
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Bone dysplasia, Azouz type | |
| fr | OBSOLETE : Dysplasie osseuse type Azouz | |
| de | OBSOLET: Skelettdysplasie Typ Azouz | |
| es | OBSOLETO: Displasia ósea tipo Azouz | |
| it | OBSOLETO: Displasia ossea, tipo Azouz | |
| nl | OBSOLEET: Botdysplasie, Azouz-type | |
| pt | OBSOLETO: Displasia óssea, tipo Azouz | |
| pl | NIEAKTUALNE: Dysplazja kosci typu Azouz | |
| cs | NEAKTUÁLNÍ: Kostní dysplázie, Azouzův typ | |
| uk | ЗАСТАРІЛО: Дисплазія кісток, тип Азуза | |
| zh | 弃用：Azouz型骨发育不良 | |
| tr | Eski adı: Kemik displazisi, Azouz 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/1844
- This record as JSON: /data/d/1844.json