ORPHA:91357
Duplication of the esophagus
- Type
- Clinical group
- 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 | Duplication of the esophagus | |
| fr | Duplication de l'oesophage | |
| de | Ösophagus-Verdoppelung | Verdopplung der Speiseröhre |
| es | Duplicación del esófago | |
| it | Duplicazione dell'esofago | |
| nl | Duplicatie van oesofagus | Duplicatie van slokdarm |
| pt | Duplicação do esófago | |
| pl | Zdwojenie przełyku | |
| cs | Duplikace jícnu | |
| uk | Дублювання стравоходу | |
| zh | 双食管 | |
| tr | Yemek borusunun duplikasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19619 | E | validated | |
| UMLS | C0266135 | 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:108959Non-syndromic esophageal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/91357
- This record as JSON: /data/d/91357.json