This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
Hypothyroidism (congenital or acquired)
HYPOTHYROIDISM
No definition available.
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 filtersNone 0 out of 7 registries used, show all original rules. |
0 |
4. Check minimum number of eventsNone |
0 |
5. Include endpoints |
54806 |
6. Filter based on genotype QC (FinnGen only) |
52929 |
Control definitions (FinnGen only)
Control exclude
NEURO_COMORBIDITIES
Extra metadata
First used in FinnGen datafreeze
DF2
Similar endpoints
↥List of similar endpoints to
Hypothyroidism (congenital or acquired)
based on the number of shared cases.
Broader endpoints:
- Disorders of the thyroid gland
- Used for control exclusion in common control thyroid runs
- Endocrine, nutritional and metabolic diseases
Narrower endpoints:
Case counts by codes
↥FinnGen case counts by registry codes:
No data for upset plot.
No data for upset table.
Summary Statistics
↥-FinRegistry-
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
-FinnGen-
Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 52929 | 42189 | 10740 |
| Unadjusted period prevalence (%) | 15.80 | 18.32 | 5.91 |
| Median age at first event (years) | 52.83 | 50.97 | 60.16 |
-FinnGen-
Age distribution of first events
-FinnGen-
Year distribution of first events
-FinnGen-
Cumulative Incidence Function
Not a core endpoint, no data to show.
Mortality – FinRegistry
↥This endpoint is excluded from FinRegistry analyses (omitted endpoint).
Relationships between endpoints
↥Index endpoint: HYPOTHYROIDISM – Hypothyroidism (congenital or acquired)
GWS hits: -
Loading Relationships table