ORPHA:141061
Commissural lip fistula
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare otorhinolaryngological malformation characterized by a unilateral or bilateral fistula located at the corner of the mouth, where the vermillion border of the upper lip meets that of the lower lip. The lesion is lined by labial mucosa. It is potentially susceptible to infection.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Commissural lip fistula | |
| fr | Fistule de la commissure labiale | |
| de | Lippenfistel, kommissurale | |
| es | Fístula en la comisura del labio | |
| it | Fistola della commissura labiale | |
| nl | Commissurale lipfistel | |
| pt | Fístula da comissura do lábio | |
| pl | Przetoka spoidła wargi | |
| cs | Komisurální píštěl rtu | |
| uk | Комісуральна нориця губи | |
| zh | 口角瘘管 | |
| tr | Komisüral dudak fistülü |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q38.0 | NTBT | attributed | validated |
| ICD-11 | LA5Y | NTBT | index | validated |
| MONDO | 0015381 | E | validated | |
| UMLS | C5680634 | E | validated | |
| GARD | 19939 | 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 (1):
- ORPHA:155835Cysts and fistulae of the face and oral cavity
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
No children.
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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/141061
- This record as JSON: /data/d/141061.json