Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Death of liver cells
Very frequent (80-99%)HP:0001404
Elevated liver enzymes
Very frequent (80-99%)HP:0002910
Hepatitis
Very frequent (80-99%)HP:0012115
Yellowing of the skin
Very frequent (80-99%)HP:0000952
Abnormal respiratory patterns
Frequent (30-79%)HP:0002793
Abnormality of the coagulation cascade
Frequent (30-79%)HP:0003256
Bruising susceptibility
Frequent (30-79%)HP:0000978
Confusion
Frequent (30-79%)HP:0001289
Diarrhea
Frequent (30-79%)HP:0002014
Elevated factor VIII level
Frequent (30-79%)HP:0030977
Emotional lability
Frequent (30-79%)HP:0000712
Factor VII deficiency
Frequent (30-79%)HP:0008169
Hepatic necrosis
Frequent (30-79%)HP:0002605
Hepatic periportal necrosis
Frequent (30-79%)HP:0002614
High blood ammonia levels
Frequent (30-79%)HP:0001987
Hypoadrenalism
Frequent (30-79%)HP:0000846
Hypotension
Frequent (30-79%)HP:0002615
Low blood sugar
Frequent (30-79%)HP:0001943
Low factor II activity
Frequent (30-79%)HP:0008151
Nausea
Frequent (30-79%)HP:0002018
Psychomotor agitation
Frequent (30-79%)HP:0000713
Reduced coagulation factor V activity
Frequent (30-79%)HP:0003225
Reduced factor X activity
Frequent (30-79%)HP:0008321
Respiratory problem
Frequent (30-79%)HP:0002795
Sleepy
Frequent (30-79%)HP:0002329
Slurred speech
Frequent (30-79%)HP:0001350
Thrombocytopenia
Frequent (30-79%)HP:0001873
Vomiting
Frequent (30-79%)HP:0002013
Absence of pain sensation
Occasional (5-29%)HP:0007021
Acidosis
Occasional (5-29%)HP:0001941
Related Conditions
Acute hepatic failure due to drugs(child)
Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein(child)
Acute hepatic failure caused by hepatitis virus(child)
Acute infantile liver failure with multisystemic involvement syndrome(child)
Autosomal recessive spinocerebellar ataxia type 21(child)
Fever-associated acute infantile liver failure syndrome(child)
Acute on chronic liver failure(child)
HRS-AKI - hepatorenal syndrome-acute kidney injury(child)
Hepatic failure(parent)
Acute digestive system disorder(parent)
Quick Facts
- SNOMED CT
- 197270009
- UMLS CUI
- C0162557
- Fully Specified Name
- Acute hepatic failure (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.