ORPHA:662456
Isolated small intestine duplication
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated small intestine duplication | |
| fr | Duplication de l'intestin grêle isolée | |
| de | Dünndarm-Duplikation, isolierte | Verdoppelung des Dünndarms |
| es | Duplicación aislada del intestino delgado | |
| it | Duplicazione dell'intestino tenue | Duplicazione dell'intestino tenue · Duplicazione dellâintestino tenue |
| nl | Geïsoleerde duplicatie van dunne darm | Duplicatie van spijsverteringsstelsel · Duplicatiecyste van dunne darm · Duplicatiecyste van voordarm · EDC · Enterale duplicatiecyste · Geïsoleerde dunnedarmduplicatie · Geïsoleerde duplicatuur van dunne darm · Intestinale duplicatie · SIDC |
| pt | Duplicação do intestino delgado isolada | |
| pl | Isolated small intestine duplication | |
| cs | Duplikace tenkého střeva | |
| uk | Подвоєння тонкої кишки | Подвоєння тонкої кишки |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q43.4 | NTBT | attributed | validated |
| ICD-11 | LB15.Y | NTBT | index | 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:108967Non-syndromic intestinal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases; rare transplant-related disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 27 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 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/662456
- This record as JSON: /data/d/662456.json