Congenital iodine-deficiency syndrome/hypothyroidism

E4_CONGEIOD

thyroid disease: A disease involving the thyroid gland.

Endpoint definition

FinnGen phenotype data

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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Check pre-conditions, main-only, mode, registry filters

Hospital Discharge: ICD-10 E00, E03.0, E03.1
Hospital discharge: ICD-9 243
Hospital discharge: ICD-8 243
Cause of death: ICD-10 E00, E03.0, E03.1
Cause of death: ICD-9 243
Cause of death: ICD-8 243

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

969

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Check minimum number of events None

969

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Include endpoints None

969

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Remove individuals based on genotype QC

935

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E4_CONGEIOD

Control definitions

Control exclude E4_THYROID

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2

Summary Statistics

Key figures

All Female Male
Number of individuals 935 740 195
Unadjusted prevalence (%) 0.23 0.32 0.11
Mean age at first event (years) 55.77 54.28 61.42

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 0.10 4.79 [2.23, 10.27] 5.7e-5 153
15 years 0.01 1.79 [0.81, 3.93] 1.5e-1 53
5 years 0.01 4.79 [2.93, 7.85] 4.9e-10 57
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

Index endpoint: E4_CONGEIOD – Congenital iodine-deficiency syndrome/hypothyroidism
GWS hits: 2

Survival analyses between endpoints

Plot

before Congenital iodine-deficiency syndrome/hypothyroidism
after Congenital iodine-deficiency syndrome/hypothyroidism

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Congenital iodine-deficiency syndrome/hypothyroidism

Endpoint not on priority list, no data to show.