gastric carcinoma: A carcinoma that arises from epithelial cells of the stomach.
Endpoint definition
↥
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
429209 |
1. Apply sex-specific ruleNone |
429209 |
2. Check conditionsNone |
429209 |
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters:
2 out of 7 registries used, show all original rules. |
2982 |
4. Check minimum number of eventsNone |
2982 |
5. Include endpointsNone |
2982 |
6. Filter based on genotype QC (FinnGen only) |
2900 |
Control definitions (FinnGen only)
Controls for this endpoint are individuals that are not cases.
Extra metadata
Similar endpoints
↥List of similar endpoints to Benign neoplasm: Stomach based on the number of shared cases.
Broader endpoints:
- Benign neoplasm: Stomach (controls excluding all cancers)
- Benign neoplasm of other and ill-defined parts of digestive system (controls excluding all cancers)
- Benign neoplasm of other and ill-defined parts of digestive system
- Benign neoplasms
- Benign neoplasms (controls excluding all cancers)
Narrower endpoints:
Case counts by codes
↥Summary Statistics
↥-FinRegistry-
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
-FinnGen-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 2900 | 1841 | 1059 |
Unadjusted period prevalence (%) | 0.72 | 0.80 | 0.58 |
Median age at first event (years) | 64.08 | 62.44 | 66.93 |
-FinnGen-
Age distribution of first events
-FinnGen-
Year distribution of first events
-FinnGen-
Cumulative Incidence Function
Mortality – FinRegistry
↥This endpoint is excluded from FinRegistry analyses (omitted endpoint).
Relationships between endpoints
↥Index endpoint: CD2_BENIGN_STOMACH – Benign neoplasm: Stomach
GWS hits: 2
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