ORPHA:101941
Rare biliary tract disease
- 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 | Rare biliary tract disease | |
| fr | Maladie rare des voies biliaires | |
| de | Gallengangkrankheit, seltene | |
| es | Enfermedad rara del tracto biliar | |
| it | Malattia rara del tratto biliare | |
| nl | Zeldzame galwegziekte | |
| pt | Doença do trato biliar, rara | |
| pl | Rzadkie choroby dróg żółciowych | |
| cs | Vzácná onemocnění žlučového traktu | |
| uk | Рідкісні захворювання жовчовивідних шляхів | |
| zh | 罕见胆道疾病 | |
| tr | Nadir safra yolu hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15116 | E | validated | |
| UMLS | C5681785 | E | validated | |
| GARD | 19791 | 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:57146Rare hepatic disease
rare hepatic diseases
Children (22):
- ORPHA:52Alagille syndrome
- ORPHA:2697Arthrogryposis-renal dysfunction-cholestasis syndrome
- ORPHA:498345Biliary atresia and associated disorders
- ORPHA:53035Caroli disease
- ORPHA:480520Caroli syndrome
- ORPHA:480501Choledochal cyst
- ORPHA:521432Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
- ORPHA:2040Congenital respiratory-biliary fistula
- ORPHA:586Cystic fibrosis
- ORPHA:300552Follicular cholangitis and pancreatitis
- ORPHA:480512Idiopathic ductopenia
- ORPHA:440987Isolated agenesis of gallbladder
- ORPHA:662388Isolated gallbladder duplication
- ORPHA:2924Isolated polycystic liver disease
- ORPHA:69663Low phospholipid-associated cholelithiasis
- ORPHA:521219Mirizzi syndrome
- ORPHA:567983Parenteral nutrition-associated cholestasis
- ORPHA:186Primary biliary cholangitis
- ORPHA:562639Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome
- ORPHA:480506Primary intrahepatic lithiasis
- ORPHA:779Reynolds syndrome
- ORPHA:447771Sclerosing cholangitis
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/101941
- This record as JSON: /data/d/101941.json