ORPHA:155899
Mandibulofacial dysostosis
Synonyms: Bilateral and symmetric oto-mandibular dysplasia
- Type
- Clinical group
- 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 | Mandibulofacial dysostosis | Bilateral and symmetric oto-mandibular dysplasia |
| fr | Dysostose mandibulo-faciale | Dysplasie oto-mandibulaire bilatérale et symétrique |
| de | Dysostose, mandibulofaziale | Dysplasie, otomandibuläre, bilaterale und symmetrische |
| es | Disóstosis mandibulofacial | Displasia oromandibular bilateral y simétrica · Displasia otomandibular bilateral y simétrica |
| it | Disostosi mandibolofacciale | Displasia otomandibolare bilaterale e simmetrica |
| nl | Mandibulofaciale dysostose | Bilaterale en symmetrische otomandibulaire dysplasie |
| pt | Disostose mandibulofacial | |
| pl | Dyzostoza żuchwowo-twarzowa | Obustronna i symetryczna dysplazja uszno-żuchwowa |
| cs | Mandibulofaciální dysostóza | Bilaterální a symetrická oto-mandibulární dysplázie |
| uk | Мандибулофаціальний дизостоз | Двобічна та симетрична дисплазія нижньої щелепи |
| zh | 下颌骨颜面发育不全 | 双侧对称性耳-下颌发育不良 |
| tr | Mandibulofasiyal dizostoz | Bilateral ve simetrik oto-mandibular displazi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q75.4 | E | specific | validated |
| ICD-11 | LD2F.16 | NTBT | index | validated |
| MONDO | 0015483 | E | validated | |
| MONDO | 15483 | E | validated | |
| MeSH | D008342 | E | validated | |
| MedDRA | 10051456 | 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:155896Otomandibular dysplasia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases; rare otorhinolaryngological diseases; rare surgical maxillo-facial diseases
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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/155899
- This record as JSON: /data/d/155899.json