ORPHA:108967
Non-syndromic intestinal 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic intestinal malformation | |
| fr | Malformation intestinale non syndromique | |
| de | Intestinale Fehlbildungen, nicht-syndromale | |
| es | Malformación intestinal no sindrómica | |
| it | Malformazione intestinale non sindromica | |
| nl | Niet-syndromale intestinale malformatie | |
| pt | Malformação intestinal não-sindromática | |
| pl | Niesyndromiczna malformacja jelit | |
| cs | Nesyndromické intestinální malformace | |
| uk | Несиндромальна кишкова вада розвитку | |
| zh | 非综合征性肠畸形 | |
| tr | Sendromik olmayan bağırsak malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15211 | E | validated | |
| UMLS | C5681766 | 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:97945Intestinal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases; rare transplant-related disorders
Children (8):
Codes that Orphanet moved or referred to this one:
- ORPHA:238OBSOLETE: Digestive duplication referred to · inactive
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/108967
- This record as JSON: /data/d/108967.json