ORPHA:294951
Congenital joint dislocations
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital joint dislocations | |
| fr | Luxation articulaire congénitale | |
| de | Gelenkdislokation, kongenitale | |
| es | Luxaciones articulares congénitas | |
| it | Dislocazioni articolari congenite | |
| nl | Congenitale gewrichtsluxaties | |
| pt | Luxações articulares congénitas | |
| pl | Wrodzone przemieszczenia stawów | |
| cs | Vrozené kloubní dislokace | |
| uk | Вроджені вивихи суглобів | |
| zh | 先天性关节脱位 | |
| tr | Doğumsal eklem çıkıkları |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17430 | E | validated | |
| UMLS | C5437774 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:109011Non-syndromic limb malformation
rare developmental anomalies during embryogenesis; rare genetic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:99666OBSOLETE: Atlantoaxial subluxation referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/294951
- This record as JSON: /data/d/294951.json