ORPHA:108965
Syndromic gastroduodenal 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 | Syndromic gastroduodenal malformation | |
| fr | Malformation gastroduodénale syndromique | |
| de | Gastroduodenale Fehlbildung, syndromale | |
| es | Malformación gastroduodenal sindrómica | |
| it | Malformazione gastroduodenale sindromica | |
| nl | Syndromale gastroduodenale malformatie | |
| pt | Malformação gastroduodenal sindromática | |
| pl | Syndromiczna malformacja żołądkowo-dwunastnicza | |
| cs | Syndromické gastroduodenální malformace | |
| uk | Синдромальна гастродуоденальна мальформація | |
| zh | 综合征性胃十二指肠畸形 | |
| tr | Sendromik gastroduodenal malformasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15210 | E | validated | |
| UMLS | C5681765 | E | validated | |
| GARD | 19858 | 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:97944Gastroduodenal 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/108965
- This record as JSON: /data/d/108965.json