Dysphagia lusoria
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
A rare aortic arch defect characterized by variable degrees of dysphagia due to compression of the esophagus from an aberrant right subclavian artery (arteria lusoria), which arises as the fourth branch, distal to the left subclavian artery, from the aortic arch. In most cases, the aberrant vessel then passes posterior to the esophagus, less frequently between the trachea and esophagus, or anterior to the trachea. Children may also present with stridor and recurrent chest infections.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dysphagia lusoria | |
| fr | Dysphagia lusoria | |
| de | Dysphagia lusoria | |
| es | Disfagia lusoria | |
| it | Disfagia lusoria | |
| nl | Dysphagia lusoria | |
| pt | Disfagia lusoria | |
| pl | Dysphagia lusoria | |
| cs | Dysphagia lusoria | |
| uk | Дисфагія lusoria | |
| zh | 食管受压性咽下困难 | |
| tr | Disfaji luzorya |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q25.8 | NTBT | attributed | validated |
| ICD-11 | LA8Y | NTBT | attributed | validated |
| MONDO | 0020418 | E | validated | |
| UMLS | C0267073 | E | validated | |
| MedDRA | 10079869 | 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:1132Aortic arch defects
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system 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/99082
- This record as JSON: /data/d/99082.json