Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Mirizzi's syndrome
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%)
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
Always present (100%)
Glucose-6-phosphate transport defect
alpha-1-Proteinase inhibitor deficiency
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 166603001
- UMLS CUI
- C0151766
- Fully Specified Name
- Liver function tests outside reference range (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.