ORPHA:141229
Facial cleft
Synonyms: Craniofacial cleft
- 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 | Facial cleft | Craniofacial cleft |
| fr | Fente faciale | Fente cranio-faciale |
| de | Gesichtsspalte | |
| es | Hendidura facial | Hendidura craneofacial |
| it | Schisi facciale | |
| nl | Aangezichtsspleet | Craniofaciale splijting |
| pt | Fenda facial | |
| pl | Rozszczep twarzy | Rozszczep twarzoczaszki |
| cs | Rozštěp obličeje | Kraniofaciální rozštěp |
| uk | Розщілина обличчя | Черепно-лицьова розщілина |
| zh | 面裂 | 颅面裂 |
| tr | Yüz yarığı | Kraniyofasiyal yarık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA51 | E | specific | validated |
| MONDO | 0015411 | E | validated | |
| MONDO | 15411 | E | validated | |
| UMLS | C5886881 | E | validated | |
| GARD | 19964 | 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 (2):
- ORPHA:155832Rare head and neck malformation
rare developmental anomalies during embryogenesis - 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/141229
- This record as JSON: /data/d/141229.json