Gilbert syndrome: An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.
Filter registries Inpat., Oupat., Death
Check pre-conditions None
Include endpoints None
Check conditions None
Apply sex-specific rule None
E4_GILBERT
Extra metadata
List of similar endpoints to
Gilbert syndrome
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 111 | 46 | 65 |
| Unadjusted prevalence (%) | 0.04 | 0.03 | 0.06 |
| Mean age at first event (years) | 42.92 | 43.27 | 42.68 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | - | - | - | - |
| 15 years | - | - | - | - |
| 5 years | - | - | - | - |
| 1 year | - | - | - | - |
Index endpoint: E4_GILBERT – Gilbert syndrome
GWS hits: 2
before Gilbert syndrome
after Gilbert syndrome
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