Overview
Abnormal liver function is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Mirizzi's syndrome
Occasional (5-29%)
Phosphoenolpyruvate carboxykinase (GTP) deficiency
Occasional (5-29%)
Bardet-Biedl syndrome
Frequent (30-79%)
Glycogen storage disease, type I
Crigler-Najjar syndrome, type I
Excluded (<1%)
Glycogen storage disease, type IV
Frequent (30-79%)
Neuroleptic malignant syndrome
Occasional (5-29%)
Primary hyperoxaluria
Frequent (30-79%)
Triglyceride storage disease with ichthyosis
Frequent (30-79%)
Hereditary fructosuria
Progressive sclerosing poliodystrophy
Frequent (30-79%)
Echinococcus multilocularis infection
Frequent (30-79%)
Cockayne syndrome
Occasional (5-29%)
Renal carnitine transport defect
Very frequent (80-99%)
Glutaric aciduria, type 2
Occasional (5-29%)
Cystathionine beta-synthase deficiency
Occasional (5-29%)
Congenital dyserythropoietic anemia, type III
Occasional (5-29%)
Fumarylacetoacetase deficiency, acute type
Gilbert's syndrome
Excluded (<1%)
Fructose-biphosphatase deficiency
Occasional (5-29%)
Crigler-Najjar syndrome
Excluded (<1%)
Cholestasis-edema syndrome, Norwegian type
Glycogen storage disease, type VI
Frequent (30-79%)
Dihydrolipoamide dehydrogenase deficiency
Occasional (5-29%)
Glucose-6-phosphate transport defect
Quick Facts
- SNOMED CT
- 75183008
- UMLS CUI
- C0086565
- Fully Specified Name
- Abnormal liver function (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.