ORPHA:98039
Digestive tract 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 | Digestive tract malformation | |
| fr | Malformation du tube digestif | |
| de | Fehlbildung des Verdauungstrakts | |
| es | Malformación del tracto digestivo | |
| it | Malformazione del tratto digestivo | |
| nl | Spijsverteringskanaalmalformatie | |
| pt | Malformação do sistema digestivo | |
| pl | Wady układu pokarmowego | |
| cs | Malformace trávicího traktu | |
| uk | Вади розвитку травного тракту | |
| zh | 消化道畸形 | |
| tr | Sindirim sistemi malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681507 | 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 (2):
- ORPHA:165711Rare abdominal surgical disease
rare abdominal surgical diseases - ORPHA:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis
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/98039
- This record as JSON: /data/d/98039.json