ORPHA:155896
Otomandibular dysplasia
- 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 | Otomandibular dysplasia | |
| fr | Dysplasie oto-mandibulaire | |
| de | Dysplasie, otomandibuläre | |
| es | Displasia otomandibular | |
| it | Displasia otomandibolare | |
| nl | Otomandibulaire dysplasie | |
| pt | Displasia otomandibular | |
| pl | Dysplazja uszno-żuchwowa | |
| cs | Otomandibulární dysplázie | |
| uk | Отомандибулярна дисплазія | |
| zh | 口下颌骨发育不良 | |
| tr | Otomandibular displazi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD2F.16 | E | specific | validated |
| MONDO | 15482 | E | validated | |
| UMLS | C5680658 | 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 (4):
- ORPHA:93453Dysostosis with predominant craniofacial involvement
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases - ORPHA:183583Genetic head and neck malformation
rare genetic diseases - ORPHA:68329Rare maxillo-facial surgical disease
rare surgical maxillo-facial diseases - ORPHA:96333Rare otorhinolaryngological malformation
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
4
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/155896
- This record as JSON: /data/d/155896.json