ORPHA:141253
Oblique facial cleft
Synonyms: Orbitofacial cleft
- Type
- Clinical group
- Group
- Group of disorders
- Age of onset
- Infancy, Neonatal
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Oblique facial cleft | Orbitofacial cleft |
| fr | Fente faciale oblique | Fente orbito-faciale |
| de | Gesichtsspalte, schräge | |
| es | Hendidura facial oblicua | Hendidura orbitofacial |
| it | Schisi facciale obliqua | |
| nl | Schuine aangezichtsspleet | Orbitofaciale spijting |
| pt | Fenda oblíqua facial | |
| pl | Skośny rozszczep twarzy | Rozszczep oczodołowo-twarzowy |
| cs | Šikmý rozštěp obličeje | Orbitofaciální rozštěp |
| uk | Коса розщілина обличчя | Орбіто-лицьова розщілина |
| zh | 斜面裂 | 眶面裂 |
| tr | Eğik yüz yarığı | Orbitofasiyal yarık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15415 | E | validated | |
| UMLS | C5679604 | 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:141229Facial cleft
rare developmental anomalies during embryogenesis; rare surgical maxillo-facial diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Prevalence at birth | 1-9 / 1 000 000 | 0.31 / 100 000 | United States | Value and class | Not yet validated | 21703590[PMID]_ORPHANET |
| Point prevalence | 1-9 / 1 000 000 | — | United States | Class only | Not yet validated | 21703590[PMID]_ORPHANET |
| Point prevalence | 1-9 / 1 000 000 | — | Europe | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/141253
- This record as JSON: /data/d/141253.json