ORPHA:97945
Intestinal malformation
Synonyms: Malformation of the intestine
- 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 | Intestinal malformation | Malformation of the intestine |
| fr | Malformation intestinale | Malformation de l'intestin |
| de | Fehlbildung, intestinale | |
| es | Malformación intestinal | Malformación del intestino |
| it | Malformazione intestinale | |
| nl | Intestinale malformatie | Malformatie van darm |
| pt | Malformação intestinal | Malformação do intestino |
| pl | Malformacja jelitowa | = en |
| cs | Střevní malformace | = en |
| uk | Кишкова вада розвитку | |
| zh | 肠道畸形 | |
| tr | Bağırsak malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681554 | 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 (3):
- ORPHA:98039Digestive tract malformation
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases - ORPHA:183545Genetic digestive tract malformation
rare genetic diseases - ORPHA:506216Rare disorder potentially indicated for bowel transplant
rare transplant-related disorders
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/97945
- This record as JSON: /data/d/97945.json