ORPHA:93280
Spondyloepiphyseal dysplasia, Omani type
inactive · moved to ORPHA:263463CHST3-related skeletal dysplasia
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to CHST3-related skeletal dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spondyloepiphyseal dysplasia, Omani type | |
| fr | Dysplasie spondyloépiphysaire type Omani | |
| de | Dysplasie, spondyloepiphysäre, Typ Omani | |
| es | Displasia espondiloepifisaria tipo Omani | |
| it | Displasia spondiloepifisaria, tipo Oman | Disostosi omero-spinale |
| nl | Spondylo-epifysaire dysplasie, Omani-type | |
| pt | Displasia espondiloepifisária, tipo Omani | |
| pl | Dysplazja kręgowo-nasadowa typu Omani | Dyzostoza ramienno-rdzeniowa |
| cs | Spondyloepifyzární dysplázie, ománský typ | Humerospinální dysostóza |
| uk | Спондилоепіфізарна дисплазія, тип Омані | |
| zh | 脊椎骨骺发育不良，Omani型 | |
| tr | Spondiloepifizyal displazi, Umman tipi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C535789 | E | validated | |
| UMLS | C1837657 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/93280
- This record as JSON: /data/d/93280.json