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Gilbert syndrome

DOID EFO MESH SNOMED PheWeb

E4_GILBERT

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

Endpoint definition

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FinnGen phenotype data

392423 individuals

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Apply sex-specific rule None

392423

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Check conditions None

392423

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Check pre-conditions, main-only, mode, registry filters

Hospital Discharge: ICD-10 E80.4
Hospital discharge: ICD-9 2774A
Hospital discharge: ICD-8 27350
Cause of death: ICD-10 E80.4
Cause of death: ICD-9 2774A
Cause of death: ICD-8 27350

2 out of 7 registries used, show all original rules.

189

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Check minimum number of events None

189

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Include endpoints None

189

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Remove individuals based on genotype QC

180

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E4_GILBERT

Control definitions

Control exclude E4_METABOLIA

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 E80
Name in latin Syndroma Gilbert

Summary Statistics

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Key figures

All Female Male
Number of individuals 180 80 100
Unadjusted prevalence (%) 0.05 0.04 0.06
Mean age at first event (years) 42.40 41.19 43.36

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

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Index endpoint: E4_GILBERT – Gilbert syndrome
GWS hits: 1

Survival analyses between endpoints

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Plot

before Gilbert syndrome
after Gilbert syndrome

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Gilbert syndrome

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Endpoint not on priority list, no data to show.