Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Increased serum gamma globulin
Always present (100%)HP:0010702
Increased total IgG in blood
Always present (100%)HP:0003237
Anti-liver cytosolic antigen type 1 antibody positivity
Very frequent (80-99%)HP:0030909
Anti-LKM1 antibody positivity
Very frequent (80-99%)HP:0030908
Antineutrophil antibody positivity
Very frequent (80-99%)HP:0003453
Antinuclear antibodies
Very frequent (80-99%)HP:0003493
Elevated serum transaminases
Very frequent (80-99%)HP:0002910
Rosette
Very frequent (80-99%)HP:0031925
Smooth muscle antibody positive
Very frequent (80-99%)HP:0003262
Abdominal discomfort
Frequent (30-79%)HP:0002027
Anti-asialoglycoprotein receptor antibody positivity
Frequent (30-79%)HP:0032469
Arthralgias
Frequent (30-79%)HP:0002829
Chronic extreme exhaustion
Frequent (30-79%)HP:0012432
Depression
Frequent (30-79%)HP:0000716
Spider hemangioma
Frequent (30-79%)HP:0012522
Acute liver inflammation
Occasional (5-29%)HP:0200119
Anxiety disease
Occasional (5-29%)HP:0000739
Blotchy loss of skin colour
Occasional (5-29%)HP:0001045
Cirrhosis
Occasional (5-29%)HP:0001394
Diffuse hepatic steatosis
Occasional (5-29%)HP:0006555
Fibrous cholangitis
Occasional (5-29%)HP:0030991
Gastrointestinal haemorrhage
Occasional (5-29%)HP:0002239
Glomerulonephritis
Occasional (5-29%)HP:0000099
Increased total bilirubin
Occasional (5-29%)HP:0003573
Inflammatory bowel disease
Occasional (5-29%)HP:0002037
Joint inflammation
Occasional (5-29%)HP:0001369
Large spleen
Occasional (5-29%)HP:0001744
Peritoneal effusion
Occasional (5-29%)HP:0001541
Thyroid gland inflammation
Occasional (5-29%)HP:0100646
Ulcerative colitis
Occasional (5-29%)HP:0100279
Related Conditions
Lupus hepatitis(child)
Autoimmune hepatitis type 1(child)
Autoimmune hepatitis type 2(child)
Autoimmune hepatitis type 3(child)
Chronic autoimmune hepatitis(child)
Primary biliary cirrhosis(child)
Autoantibody negative autoimmune hepatitis(child)
Primary biliary cholangitis and/or primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome(child)
Autoimmune liver disease(parent)
Inflammatory disorder of liver(parent)
Quick Facts
- SNOMED CT
- 408335007
- UMLS CUI
- C4721555
- Fully Specified Name
- Autoimmune hepatitis (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.