ORPHA:35063
Fulminant viral hepatitis
- Type
- Disease
- Group
- Disorder
- Status
- active
Fulminant viral hepatitis is a rapid and severe impairment of liver functions (acute liver failure) with hepatic encephalopathy developing less than 8 weeks after the onset of jaundice, secondary to viral hepatitis mainly due to HBV, but also to HAV.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fulminant viral hepatitis | |
| fr | Hépatite virale fulminante | |
| de | Virushepatitis, fulminante | |
| es | Hepatitis viral fulminante | |
| it | Epatite virale fulminante | |
| nl | Fulminante virale hepatitis | |
| pt | Hepatite vírica fulminante | |
| pl | Piorunujące wirusowe zapalenie wątroby | |
| cs | Fulminantní virová hepatitida | |
| uk | Фульмінантний вірусний гепатит | |
| zh | 暴发性病毒性肝炎 | |
| tr | Fulminan viral hepatit |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K72 | NTBT | inclusion | validated |
| ICD-11 | 1E50.Y | NTBT | index | validated |
| MONDO | 0018109 | E | validated | |
| UMLS | C0276624 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:506210Rare disorder potentially indicated for liver transplant
rare transplant-related disorders - ORPHA:101939Rare parenchymal liver disease
rare hepatic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/35063
- This record as JSON: /data/d/35063.json