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Gilbert syndrome

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


Explore Associated Targets
Mondo Description An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
Uniprot Description Occurs as a consequence of reduced bilirubin transferase activity and is often detected in young adults with vague non-specific complaints.
Disease Ontology Description A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity.
Mondo Term and Equivalent IDs
MONDO:0007745:  Gilbert syndrome
COHD:4099740: 
EFO:0005556: 
GARD:0006507: 
ICD10:E80.4: 
MESH:D005878: 
NCIT:C84729: 
SCTID:27503000: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)