ORPHA:156252
Tracheal anomaly
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Tracheal anomaly | |
| fr | Anomalie de la trachée | |
| de | Trachealanomalie | Luftröhrenanomalie |
| es | Anomalía traqueal | |
| it | Anomalia della trachea | |
| nl | Tracheale anomalie | |
| pt | Anomalia da traqueia | |
| pl | Wada tchawicy | |
| cs | Anomálie trachey | |
| uk | Аномалія трахеї | |
| zh | 气管畸形 | |
| tr | Trakeal anomali |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA73 | E | specific | validated |
| MONDO | 15505 | E | validated | |
| UMLS | C5680647 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:96333Rare otorhinolaryngological malformation
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
4
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/156252
- This record as JSON: /data/d/156252.json