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
Frequent (30-79%)
Yellow fever
Occasional (5-29%)
Hereditary fructosuria
Congenital dyserythropoietic anemia, type III
Frequent (30-79%)
Rotor syndrome
Frequent (30-79%)
Rh deficiency syndrome
Frequent (30-79%)
Hereditary spherocytosis
Frequent (30-79%)
Congenital dyserythropoietic anemia, type I
Always present (100%)
Malaria
Frequent (30-79%)
Glycogenosis with glucoaminophosphaturia
Frequent (30-79%)
Infantile nephropathic cystinosis
Frequent (30-79%)
Congenital atresia of extrahepatic bile duct
Wilson's disease
Always present (100%)
Congenital absence of thyroid gland
Disease caused by Plasmodiidae
Frequent (30-79%)
Cystinosis
Frequent (30-79%)
ABL - Abetalipoproteinaemia
Frequent (30-79%)
Westphal-Strumpell syndrome
Always present (100%)
Hereditary ovalocytosis
Occasional (5-29%)
Graft versus host disease
Occasional (5-29%)
Intrahepatic cholestasis of pregnancy
Occasional (5-29%)
Generalized thyroid hormone resistance
Fumarase deficiency
Pearson's syndrome
Occasional (5-29%)
Delta-4-3-oxosteroid-5-beta-reductase deficiency
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 26165005
- UMLS CUI
- C0311468
- Fully Specified Name
- Bilirubin level above 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.