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
↥
FinnGen phenotype data
392423 individuals
Apply sex-specific rule None
392423
Check conditions None
392423
Check pre-conditions, main-only, mode, registry filters None
0 out of 7 registries used, show all original rules.
0
Check minimum number of events None
0
Include endpoints
49302
Remove individuals based on genotype QC
47665
HYPOTHYROIDISM
Control definitions
Control exclude
NEURO_COMORBIDITIES
Extra metadata
First used in FinnGen datafreeze
DF2
No data for upset plot.
No data for upset table.
Similar endpoints
↥List of similar endpoints to
Hypothyroidism (congenital or acquired)
based on the number of shared cases.
Broader endpoints:
- Hypothyreosis and Thyroxine purchase for inclusion criteria
- Disorders of the thyroid gland
- Used for control exclusion in common control thyroid runs
- Endocrine, nutritional and metabolic diseases
- Co-morbidities of interest (NEURO)
Narrower endpoints:
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 47665 | 38007 | 9658 |
| Unadjusted prevalence (%) | 12.64 | 18.03 | 5.81 |
| Mean age at first event (years) | 51.69 | 50.01 | 58.32 |
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: HYPOTHYROIDISM – Hypothyroidism (congenital or acquired)
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Hypothyroidism (congenital or acquired)
↥Endpoint not on priority list, no data to show.