Third branchial cleft anomaly
Synonyms: Third branchial cleft cyst · Third branchial cleft fistula
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare otorhinolaryngeal malformation characterized by a soft, fluctuant mass, abscess or draining tract along the anterior border of the lower half of sternocleidomastoid muscle, occasionally leading to development of retropharyngeal abscess, acute suppurative thyroiditis, stridor, respiratory distress, odynophagia, and dysphagia. Anomaly occurs as a tract from the piriform sinus to the thyroid gland. A third branchial cleft fistula passes superficial to both the superior and recurrent laryngeal nerves, which is the main difference in comparison to the fourth branchial cleft fistula.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Third branchial cleft anomaly | Third branchial cleft cyst · Third branchial cleft fistula |
| fr | Anomalie de la troisième fente branchiale | Fistule de la troisième fente branchiale · Kyste de la troisième fente branchiale |
| de | Kiemenbogen, 3., Anomalie des | |
| es | Anomalía de la tercera hendidura branquial | Fístula de la tercera hendidura branquial · Quiste de la tercera hendidura branquial |
| it | Schisi del terzo arco branchiale | |
| nl | Anomalie van derde kieuwspleet | Cyste van derde kieuwspleet · Fistel van derde kieuwspleet |
| pt | Anomalia da terceira fenda branquial | |
| pl | Anomalia trzeciego łuku skrzelowego | Przetoka trzeciego łuku skrzelowego · Torbiel trzeciego łuku skrzelowego |
| cs | Anomálie třetí branchiální štěrbiny | Cysta třetí branchiální štěrbiny · Píštěl třetí branchiální štěrbiny |
| uk | Аномалія третьої зябрової щілини | Третя гілкова щілинна кіста · Третя гілкова щілинна нориця |
| zh | 第三鳃裂畸形 | 第三鳃裂瘘管 |
| tr | Üçüncü brankial yarık anomalisi | Üçüncü branşiyal yarık kisti · Üçüncü branşiyal yarık fistülü |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q18.0 | NTBT | attributed | validated |
| MONDO | 0015377 | E | validated | |
| UMLS | C3874314 | E | validated | |
| GARD | 19935 | 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:155835Cysts and fistulae of the face and oral cavity
rare developmental anomalies during embryogenesis; rare otorhinolaryngological 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/141030
- This record as JSON: /data/d/141030.json