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Acute liver failure
Disease definition
A rare hepatic disease characterized by acute onset of severe liver dysfunction without evidence of underlying chronic liver disease. Patients present with nonspecific symptoms like jaundice, upper right abdominal pain, nausea, vomiting, pruritus, fatigue, and fever. The condition may rapidly progress to hepatic encephalopathy, coagulopathy, and life-threatening multiorgan failure. Liver biopsy typically shows massive hepatic necrosis.
ORPHA:90062
Classification level: Disorder- Synonym(s):
- Acute hepatic failure
- Fulminant hepatic failure
- Prevalence: 1-5 / 10 000
- Inheritance: Not applicable
- Age of onset: Infancy, Childhood, Adolescent, Adult, Elderly
- ICD-10: K72.0
- OMIM: -
- UMLS: C0162557
- MeSH: D017114
- GARD: -
- MedDRA: 10000804
A summary on this disease is available in Español (2020) Français (2020) Nederlands (2020)
Detailed information
Guidelines
- Clinical practice guidelines
- English (2017) - J Hepatol
- English (2020) - Nat Rev Gastroenterol Hepatol


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.