ORPHA:210581
Temporomandibular joint anomaly
- 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 | Temporomandibular joint anomaly | |
| fr | Anomalie temporo-mandibulaire | |
| de | Temporomandibuläre Gelenkstörung | |
| es | Anomalía de la articulación temporomandibular | |
| it | Anomalia dell'articolazione temporo-mandibolare | |
| nl | Temporomandibulair gewricht-anomalie | |
| pt | Anomalia das articulações temporomandibulares | |
| pl | Wada stawu skroniowo-żuchwowego | |
| cs | Anomálie temporomandibulárního kloubu | |
| uk | Аномалія скронево-нижньощелепного суглоба | |
| zh | 颞下颌关节异常 | |
| tr | Temporomandibular eklem anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | DA0E.8 | NTBT | index | validated |
| MONDO | 16221 | E | validated | |
| UMLS | C1865318 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:68329Rare maxillo-facial surgical disease
rare surgical maxillo-facial diseases
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/210581
- This record as JSON: /data/d/210581.json