ORPHA:662376
Isolated gastric duplication
Synonyms: Isolated stomach duplication
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Childhood, Infancy, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated gastric duplication | Isolated stomach duplication |
| fr | Duplication gastrique isolée | Duplication de l'estomac isolée |
| de | Magen-Duplikation, isolierte | Isolierte Verdoppelung des Magens · Verdoppelung des Magens |
| es | Duplicación gástrica aislada | Duplicación aislada del estómago |
| it | Duplicazione gastrica | Duplicazione dello stomaco |
| nl | Geïsoleerde duplicatie van maag | Geïsoleerde maagduplicatuur |
| pt | Duplicação gástrica isolada | Duplicação do estômago isolada |
| pl | Isolated gastric duplication | = en |
| cs | Duplikace žaludku | = en |
| uk | Подвоєння шлунка | Подвоєння шлунка |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q40.2 | NTBT | inclusion | validated |
| UMLS | C0266148 | 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:108963Non-syndromic gastroduodenal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Prevalence at birth | 1-9 / 100 000 | 1.7 / 100 000 | Worldwide | Value and class | Validated | 18558208[PMID]_ORPHANET |
| Point prevalence | 1-9 / 100 000 | 1.7 / 100 000 | Worldwide | Value and class | Validated | 18558208[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/662376
- This record as JSON: /data/d/662376.json