Gilbert syndrome: An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
| Name | E4_GILBERT |
|---|---|
| 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 |
| 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 |
| 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 |
before Gilbert syndrome
after Gilbert syndrome
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