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 | 54 | 19 | 35 |
| Unadjusted prevalence (%) | 0.04 | 0.03 | 0.06 |
| Mean age at first event (years) | 44.22 | 47.65 | 42.36 |
| Median number of events / individual | 1 | 1 | 1 |
Clinical metrics
| Sex | All | Female | Male |
| Recurrence within 6 months (%) | 22.22 | 26.32 | 20.0 |
| Case fatality at 5-years (%) | 1.85 | 0.0 | 2.86 |