ORPHA:498350
Syndromic biliary atresia
- Type
- Clinical group
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndromic biliary atresia | |
| fr | Atrésie des voies biliaires syndromique | |
| de | Gallengangatresie, syndromatische | |
| es | Atresia biliar síndrómica | |
| it | Atresia biliare sindromica | |
| nl | Syndromale biliaire atresie | |
| pt | Atresia biliar sindromática | |
| pl | Zespół atrezji dróg żółciowych | |
| cs | Syndromická biliární atrézie | |
| uk | Синдромальна біліарна атрезія | |
| zh | 综合征性胆道闭锁 | |
| tr | Sendromik biliyer atrezi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681237 | 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:498345Biliary atresia and associated disorders
rare hepatic 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/498350
- This record as JSON: /data/d/498350.json