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Congenital iodine-deficiency syndrome/hypothyroidism

DOID EFO Endpoint Browser PheWeb

E4_CONGEIOD

Endpoint definition

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Endpoint definition steps

FinnGen

Phenotype data

429209

1. Apply sex-specific rule

None

429209

2. Check conditions

None

429209

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

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

4. Check minimum number of events

None

969

5. Include endpoints

None

969

6. Filter based on genotype QC (FinnGen only)

935

Control definitions (FinnGen only)

Control exclude E4_THYROID

Extra metadata

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

Case counts by codes

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FinnGen case counts by registry codes:

generic upset plot

Upset plot

Full data table

Summary Statistics

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-FinRegistry-

Key figures

All Female Male
Number of individuals
Whole population 11024 8810 2178
Only index persons 10110 8174 1936
Unadjusted period prevalence (%)
Whole population 0.21 0.25 0.06
Only index persons 0.26 0.30 0.07
Median age at first event (years)
Whole population 67.75 68.82 63.38
Only index persons 67.54 68.52 63.45

-FinnGen-

Key figures

All Female Male
Number of individuals 935 740 195
Unadjusted period prevalence (%) 0.28 0.32 0.11
Median age at first event (years) 61.03 59.77 65.80

-FinRegistry-

Age distribution of first events

-FinnGen-

Age distribution of first events

-FinRegistry-

Year distribution of first events

-FinnGen-

Year distribution of first events

-FinRegistry-

Cumulative Incidence Function

-FinnGen-

Cumulative Incidence Function

Mortality – FinRegistry

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Relationships between endpoints

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

GWS hits: 2

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