ORPHA:156607
Genetic 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 | Genetic biliary tract disease | |
| fr | Maladie génétique du tractus biliaire | |
| de | Gallengangkrankheit, genetisch bedingte | |
| es | Enfermedad genética del tracto biliar | |
| it | Malattia genetica del tratto biliare | |
| nl | Genetische galwegziekte | |
| pt | Doença do trato biliar, genética | |
| pl | Genetyczna choroba dróg żółciowych | |
| cs | Geneticky podmíněné nemoci žlučových cest | |
| uk | Генетично обумовлені захворювання жовчовивідних шляхів | |
| zh | 遗传性胆道疾病 | |
| tr | Genetik safra yolu hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15509 | E | validated | |
| UMLS | C5680643 | 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:156601Rare genetic hepatic disease
rare genetic diseases
Children (10):
- ORPHA:52Alagille syndrome
- ORPHA:2697Arthrogryposis-renal dysfunction-cholestasis syndrome
- ORPHA:53035Caroli disease
- ORPHA:480520Caroli syndrome
- ORPHA:521432Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
- ORPHA:586Cystic fibrosis
- ORPHA:480556Isolated neonatal sclerosing cholangitis
- ORPHA:2924Isolated polycystic liver disease
- ORPHA:69663Low phospholipid-associated cholelithiasis
- ORPHA:59303Neonatal ichthyosis-sclerosing cholangitis syndrome
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/156607
- This record as JSON: /data/d/156607.json