Tessier number 5 facial cleft
- Type
- Morphological anomaly
- Group
- Disorder
- Age of onset
- Antenatal, Neonatal
- Status
- active
A rare oblique facial cleft characterized by a congenital unilateral or bilateral defect beginning in the upper lip medial to the oral commissure and extending across the cheek as a groove ending between the middle and lateral third of the lower eyelid (resulting in coloboma). Bone involvement includes an alveolar cleft in the premolar region, extending across the maxilla lateral to the infraorbital nerve and up to the infraorbital rim and orbital floor. The malformation may be associated with Tessier number 3 and number 4 clefts, macrostomia, or anophthalmos.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Tessier number 5 facial cleft | |
| fr | Fente faciale 5 de Tessier | |
| de | Gesichtsspalte, Tessier 5 | |
| es | Hendidura facial número 5 de Tessier | |
| it | Schisi facciale di Tessier numero 5 | |
| nl | Aangezichtsspleet Tessier nummer 5 | |
| pt | Fenda facial número 5 de Tessier | |
| pl | Rozszczep twarzy numer 5 wg Tessiera | |
| cs | Rozštěp obličeje číslo 5 dle Tessiera | |
| uk | Розщілина обличчя Тессьє №5 | |
| zh | Tessier5型面裂 | |
| tr | Tessier 5 numaralı yüz yarığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q18.8 | NTBT | attributed | validated |
| ICD-11 | LA51 | NTBT | index | validated |
| MONDO | 0015416 | E | validated | |
| UMLS | C0432119 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:141253Oblique facial cleft
rare developmental anomalies during embryogenesis; rare surgical maxillo-facial diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/141261
- This record as JSON: /data/d/141261.json