Gilbert syndrome

Gilbert syndrome: An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.

Endpoint definition

Long name Gilbert syndrome
Hospital Discharge registry ICD-10: E804, ICD-9: 2774A, ICD-8: 27350
Cause of Death registry ICD-10: E804, ICD-9: 2774A, ICD-8: 27350
Level in the ICD-hierarchy 4
First defined in version DF2
Latin name Syndroma Gilbert

Summary Statistics

Key figures

All Female Male
Number of individuals 88 32 56
Unadjusted prevalence (%) 0.04 0.03 0.06
Mean age at first event (years) 42.76 44.58 41.72
Case fatality at 5-years (%) 4.55 0.00 7.14

Longitudinal metrics

All Female Male
Median nb. of events per indiv. 1.0 1.0 1.0
Recurrence at 6 months (%) 18.18 15.63 19.64

Survival analyses between endpoints


before Gilbert syndrome
after Gilbert syndrome

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Drugs most likely to be purchased after Gilbert syndrome