Biliary chirrosis, primary
Description
primary biliary cirrhosis: Primary biliary cholangitis (PBC) is a chronic and slowly progressive cholestatic liver disease of autoimmune etiology characterized by injury of the intrahepatic bile ducts that may eventually lead to liver failure.
Data source
| FinnGen phenocode | CHIRBIL_PRIM |
| Hospital Discharge registry | ICD-10: K743 |
| Cause of Death registry | ICD-10: K743 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 201 | 176 | 25 |
| Unadjusted prevalence (%) | 0.12 | 0.18 | 0.03 |
| Mean age at first event (years) | 56.54 | 56.45 | 57.18 |
| Case fatality at 5-years (%) | 3.98 | 3.41 | 8.0 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 7 | 7 | 6 |
| Recurrence at 6 months (%) | 78.11 | 78.98 | 72.0 |
Associations
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