ORPHA:68329
Rare maxillo-facial surgical disease
Synonyms: Rare maxillofacial anomaly
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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 | Rare maxillo-facial surgical disease | Rare maxillofacial anomaly |
| fr | Maladie rare en chirurgie maxillo-faciale | Anomalie maxillo-faciale rare |
| de | Seltene Krankheit der Maxillo-fazialen Chirurgie | |
| es | Anomalía maxilofacial rara | |
| it | Anomalia maxillofacciale rara | |
| nl | Zeldzame maxillo-faciale chirurgische ziekte | Zeldzame maxillofaciale anomalie |
| pt | Doença cirúrgica maxilofacial rara | Anomalia maxilofacial rara |
| pl | Rzadkie choroby chirurgiczne szczękowo-twarzowe | Rzadkie wady szczękowo-twarzowe |
| cs | Vzácná maxilofaciální chirurgická onemocnění | Vzácné maxilofaciální anomálie |
| uk | Рідкісне щелепно-лицьове хірургічне захворювання | Рідкісна щелепно-лицева аномалія |
| zh | 罕见颌面手术疾病 | 罕见颌面异常 |
| tr | Nadir çene-yüz cerrahisi hastalığı | Nadir maksillofasiyal anomali |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19038 | E | validated | |
| UMLS | C5680147 | 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.
Children (11):
- ORPHA:1991Cleft lip with or without cleft palate
- ORPHA:2014Cleft palate
- ORPHA:141229Facial cleft
- ORPHA:156212Hypoglossia/aglossia
- ORPHA:156207Macroglossia
- ORPHA:306553Myospherulosis
- ORPHA:357154Oral submucous fibrosis
- ORPHA:155896Otomandibular dysplasia
- ORPHA:156224Paralytic facial malformation
- ORPHA:156237Syndrome or malformation associated with head and neck malformations
- ORPHA:210581Temporomandibular joint anomaly
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/68329
- This record as JSON: /data/d/68329.json