Idiopathic pulmonary fibrosis (attempt to specificity)
Description
idiopathic pulmonary fibrosis: Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause.
Data source
| FinnGen phenocode | IPF |
| Hospital Discharge registry | ICD-10: J841 |
| Cause of Death registry | ICD-10: J841 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 795 | 319 | 476 |
| Unadjusted prevalence (%) | 0.46 | 0.32 | 0.63 |
| Mean age at first event (years) | 68.95 | 67.55 | 69.88 |
| Case fatality at 5-years (%) | 20.63 | 16.61 | 23.32 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 4 | 4 | 4 |
| Recurrence at 6 months (%) | 64.53 | 63.64 | 65.13 |
Associations
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