ORPHA:168448
Spondyloepimetaphyseal dysplasia, Bieganski type
inactive · moved to ORPHA:83629Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Leukoencephalopathy-spondyloepimetaphyseal dysplasia syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spondyloepimetaphyseal dysplasia, Bieganski type | |
| fr | Dysplasie spondylo-épimétaphysaire type Bieganski | |
| de | Dysplasie, spondyloepimetaphysäre, Typ Bieganski | |
| es | Displasia espondiloepimetafisaria tipo Bieganski | |
| it | Displasia spondiloepimetafisaria, tipo Bieganski | |
| nl | Spondylo-epimetafysaire dysplasie, Bieganski-type | |
| pt | Displasia espondiloepimetafisária, tipo Bieganski | |
| pl | Dysplazja kręgowo-nasadowo-przynasadowa, typ Bieganskiego | |
| cs | Spondyloepimetafyzární dysplázie, Bieganskiho typ | |
| uk | Спондилоепіметафізарна дисплазія, тип Беганського | |
| zh | Bieganski 型脊柱动脉炎性发育不良 | |
| tr | Spondiloepimetafizyal displazi, Bieganski 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/168448
- This record as JSON: /data/d/168448.json