Gilbert syndrome
Description
Gilbert syndrome: An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
Data source
| FinnGen phenocode | E4_GILBERT |
| 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 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 72 | 27 | 45 |
| Unadjusted prevalence (%) | 0.04 | 0.03 | 0.06 |
| Mean age at first event (years) | 43.77 | 45.92 | 42.48 |
| Case fatality at 5-years (%) | 4.17 | 0.0 | 6.67 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 1 | 1 | 1 |
| Recurrence at 6 months (%) | 18.06 | 18.52 | 17.78 |
Associations
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