This is a non-core endpoint: only basic statistics are computed.
See its core counterpart CD2_BENIGN_EXALLC for full statistics.
Benign neoplasms
CD2_BENIGN
No definition available.
Endpoint definition
↥
FinnGen phenotype data
392423 individuals
Apply sex-specific rule None
392423
Check conditions None
392423
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
88584
Check minimum number of events None
88584
Include endpoints
103442
Remove individuals based on genotype QC
100058
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:
- Benign neoplasms (controls excluding all cancers)
- Any event in hilmo or specialist outpatient
- Any ICDMAIN event in hilmo or causes of death
Narrower endpoints:
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 100058 | 68815 | 31243 |
| Unadjusted prevalence (%) | 26.53 | 32.64 | 18.79 |
| Mean age at first event (years) | 50.66 | 47.28 | 58.12 |
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.