ORPHA:57146
Rare hepatic disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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 hepatic disease | |
| fr | Maladie hépatique rare | |
| de | Leberkrankheit, seltene | |
| es | Enfermedad hepática rara | |
| it | Malattia epatica rara | |
| nl | Zeldzame hepatische ziekte | |
| pt | Doença hepática rara | |
| pl | Rzadkie choroby wątroby | |
| cs | Vzácná onemocnění jater | |
| uk | Рідкісні захворювання печінки | |
| zh | 罕见肝病 | |
| tr | Nadir karaciğer hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18928 | E | validated | |
| UMLS | C5681272 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
Children (13):
- ORPHA:90062Acute liver failure
- ORPHA:1414Cholestasis-lymphedema syndrome
- ORPHA:244242HELLP syndrome
- ORPHA:90073Hepatitis B reinfection following liver transplantation
- ORPHA:402823Hepatitis delta
- ORPHA:276405Hyperbiliverdinemia
- ORPHA:101941Rare biliary tract disease
- ORPHA:101943Rare hepatic and biliary tract tumor
- ORPHA:101940Rare metabolic liver disease
- ORPHA:101939Rare parenchymal liver disease
- ORPHA:101938Rare vascular liver disease
- ORPHA:90052Recurrent hepatitis C virus induced liver disease in liver transplant recipients
- ORPHA:2312Transient familial neonatal hyperbilirubinemia
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/57146
- This record as JSON: /data/d/57146.json