ORPHA:662388
Isolated gallbladder duplication
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated gallbladder duplication | |
| fr | Duplication isolée de la vésicule biliaire | |
| de | Gallenblasen-Duplikation, isolierte | |
| es | Duplicación aislada de la vesícula biliar | |
| it | Duplicazione della cistifellea | |
| nl | Geïsoleerde duplicatie van galblaas | Geïsoleerde duplicatuur van galblaas |
| pt | Duplicação da vesícula biliar isolada | |
| pl | Isolated gallbladder duplication | |
| cs | Duplikace žlučníku | |
| uk | Подвоєння жовчного міхура |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q44.1 | NTBT | attributed | validated |
| ICD-11 | LB20.1Y | NTBT | index | validated |
| UMLS | C0266250 | 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 (2):
- ORPHA:108971Non-syndromic visceral malformation of the liver, biliary tract, pancreas or spleen
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases; rare transplant-related disorders - ORPHA:101941Rare biliary tract disease
rare hepatic diseases
No children.
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/662388
- This record as JSON: /data/d/662388.json