This is a non-core endpoint: only basic statistics are computed.
Malignant neoplasms of independent (primary) multiple sites
CD2_INDEPENDENT_MULTIPLE_SITES_NAS_EXALLC
No definition available.
Endpoint definition
↥
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
|
1. Apply sex-specific ruleNone |
- |
2. Check conditionsNone |
|
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters: 2 out of 7 registries used, show all original rules. |
- |
4. Check minimum number of eventsNone |
- |
5. Include endpointsNone |
- |
6. Filter based on genotype QC (FinnGen only)None |
- |
Control definitions (FinnGen only)
- Control exclude
- C3_CANCER, C3_CANCER_WIDE
Extra metadata
- Level in the ICD hierarchy
- 3
- First used in FinnGen datafreeze
- DF2
- Parent code in ICD-10
- C97-C97
- Name in latin
- Neoplasmata maligna locis multis non dependentibus (primariis)
Similar endpoints
↥List of similar endpoints to
Malignant neoplasms of independent (primary) multiple sites
based on the number of shared cases.
Similar with more cases:
- Malignant neoplasms of independent (primary) multiple sites
- Malignant neoplasm
- Malignant neoplasm, excluding all cancers (controls excluding all cancers)
- Malignant neoplasm, wide definition for exclusion
- Malignant neoplasm, wide definition for exclusion, excluding all cancers (controls excluding all cancers)
Similar with less cases:
Case counts by codes
↥FinnGen case counts by registry codes:
No upset plot: script not run.
No upset table: script not run.
Summary Statistics
↥-FinRegistry-
This endpoint is excluded (different definition than used in FinnGen).
-FinnGen-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 20 | 8 | 12 |
Unadjusted period prevalence (%) | 0.00 | 0.00 | 0.01 |
Median age at first event (years) | 59.50 | 45.23 | 69.01 |
-FinnGen-
Age distribution of first events
-FinnGen-
Year distribution of first events
-FinnGen-
Cumulative Incidence Function
Not a core endpoint, no data to show.
CodeWAS (R11)
↥CodeWAS is a tool for exploring the associations between an endpoint and all of the medical codes and drug codes.
This is a new tool, please reach out using the contact form for feedback and improvement ideas.
First, a cohort is built by matching controls to the endpoint cases using year of birth and sex. Then, a Fisher test is done for all the medical codes and drug codes between the cases and controls of this cohort. Codes are reported in the table below if they have −log10(p-value) ≥ 6.
No data available
LabWAS
↥Mortality – FinRegistry
↥This endpoint is excluded (different definition than used in FinnGen).
Relationships between endpoints
↥Index endpoint: CD2_INDEPENDENT_MULTIPLE_SITES_NAS_EXALLC – Malignant neoplasms of independent (primary) multiple sites
GWS hits: -
This endpoint is excluded (different definition than used in FinnGen).