Tessier number 6 facial cleft
- Type
- Morphological anomaly
- Group
- Disorder
- Age of onset
- Antenatal, Neonatal
- Status
- active
A rare oblique facial cleft characterized by a defect between the maxilla and the zygomatic bone, opening into the infra-orbital fissure, accompanied by coloboma of the lower eyelid and a vertical furrow on the cheek oriented either laterally to the corner of the mouth or in the direction of the angle of the mandible. The posterior aspect of the maxilla is short with a high palate and choanal atresia. The malformation is typically associated with Treacher-Collins syndrome.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Tessier number 6 facial cleft | |
| fr | Fente faciale 6 de Tessier | |
| de | Gesichtsspalte, Tessier 6 | |
| es | Hendidura facial número 6 de Tessier | |
| it | Schisi facciale di Tessier, numero 6 | |
| nl | Aangezichtsspleet Tessier nummer 6 | |
| pt | Fenda facial número 6 de Tessier | |
| pl | Rozszczep twarzy numer 6 wg Tessiera | |
| cs | Rozštěp obličeje číslo 6 dle Tessiera | |
| uk | Розщілина обличчя Тессьє №6 | |
| zh | Tessier6型面裂 | |
| tr | Tessier 6 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 | 0015417 | E | validated | |
| UMLS | C0432120 | 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/141265
- This record as JSON: /data/d/141265.json