Recurrent hepatitis C virus induced liver disease in liver transplant recipients
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare hepatic disease characterized by recurrence of hepatitis C virus infection after liver transplantation, leading to liver injury with features resembling those observed in the non-transplant graft, and typically developing after three months post-transplantation. The clinical course is highly variable, although patients most commonly develop progressive chronic liver disease with higher viral loads and more rapid fibrosis progression than in the immunocompetent population.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Recurrent hepatitis C virus induced liver disease in liver transplant recipients | |
| fr | Manifestations hépatiques récurrentes causées par le virus de l'hépatite C chez les transplantés hépatiques | |
| de | Rekurrente Hepatitis-C-Virus-induzierte Lebererkrankung bei Lebertransplantierten | |
| es | Enfermedad hepática por recurrencia del virus de la hepatitis C en trasplantados hepáticos | |
| it | Epatiti ricorrenti da virus dell'epatite C nei pazienti trapiantati di fegato | |
| nl | Terugkerende hepatitis C-virus-geïnduceerde leverziekte bij levertransplantaatrecipiënten | |
| pt | Doença hepática recorrente induzida pelo vírus da Hepatite C em recetores de transplante hepático | |
| pl | Nawracające zapalenie wątroby typu C indukujące chorobę wątroby u biorców przeszczepionej wątroby | |
| cs | Rekurentní postižení jater indukované virem hepatitidy C u příjemců transplantátu | |
| uk | Рецидивуючі захворювання печінки, спричинені вірусом гепатиту С, у реципієнтів трансплантації печінки | |
| zh | 复发性丙型肝炎病毒所致肝移植受者肝病 | |
| tr | Karaciğer nakli alıcılarında tekrarlayan hepatit C virüsünün neden olduğu karaciğer hastalığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B18.2 | NTBT | attributed | validated |
| ICD-11 | 1E51.1 | NTBT | attributed | validated |
| UMLS | C5681349 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
rare transplant-related disorders - ORPHA:57146Rare hepatic disease
rare hepatic diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 7 / 100 000 | Europe | Value and class | Validated | European Medicines Agency[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/90052
- This record as JSON: /data/d/90052.json