ORPHA:108961
Syndromic esophageal malformation
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndromic esophageal malformation | |
| fr | Malformation syndromique de l'oesophage | |
| de | Ösophagusfehlbildung, syndromale | |
| es | Malformaciones esofágicas sindrómicas | |
| it | Malformazioni sindromiche dell'esofago | |
| nl | Syndromale oesofageale malformatie | |
| pt | Malformação esofágica sindromática | |
| pl | Syndromiczna malformacja przełyku | |
| cs | Syndromické malformace jícnu | |
| uk | Синдромальна вада розвитку стравоходу | |
| zh | 综合征性食管畸形 | |
| tr | Sendromik özofagus malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15208 | E | validated | |
| UMLS | C5681763 | E | validated | |
| GARD | 19856 | 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:88993Esophageal malformation
rare developmental anomalies during embryogenesis; 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/108961
- This record as JSON: /data/d/108961.json