This is a non-core endpoint: only basic statistics are computed.
See its core counterpart CD2_BENIGN_EXALLC for full statistics.
Endpoint definition
↥
FinnGen phenotype data
429209 individuals
Apply sex-specific rule None
429209
Check conditions None
429209
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
97350
Check minimum number of events None
97350
Include endpoints
113162
Remove individuals based on genotype QC
109348
CD2_BENIGN
Control definitions
Controls for this endpoint are individuals that are not cases.
Extra metadata
Level in the ICD hierarchy
1
First used in FinnGen datafreeze
DF2
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to
Benign neoplasms
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 109348 | 75133 | 34215 |
| Unadjusted prevalence (%) | 26.54 | 32.63 | 18.83 |
| Mean age at first event (years) | 50.56 | 47.21 | 57.94 |
Mortality
Not a core endpoint, no data to show.
Age distribution of first events
Year distribution of first events
Cumulative Incidence
Not a core endpoint, no data to show.
Correlations
↥
Index endpoint: CD2_BENIGN – Benign neoplasms
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Benign neoplasms
↥Endpoint not on priority list, no data to show.