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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

414262 individuals

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Apply sex-specific rule None

414262

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Check conditions None

414262

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Check pre-conditions, main-only, mode, registry filters None

0 out of 7 registries used, show all original rules.

0

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Check minimum number of events None

0

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Remove individuals based on genotype QC

47665

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HYPOTHYROIDISM

Control definitions

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.

Venn diagram with an highlighted set fully inside another set Broader endpoints:

Venn diagram with a set fully inside an highlighted set Narrower endpoints:

Show all endpoint correlations

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)

Not a core endpoint, no data to show.