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This is a non-core endpoint: only basic statistics are computed.

Hyperimmunoglobulin E [IgE] syndrome

D3_HYPERIGESDR

obsolete_Job's syndrome: ['Primary immunodeficiency syndrome characterized by recurrent infections and hyperimmunoglobulinemia E. Most cases are sporadic. Of the rare familial forms, the dominantly inherited subtype has additional connective tissue, dental and skeletal involvement that the recessive type does not share.']

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 D82.4
Cause of death: ICD-10 D82.4

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

18

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Check minimum number of events None

18

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Include endpoints None

18

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Remove individuals based on genotype QC

17

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D3_HYPERIGESDR

Control definitions

Control exclude D3_IMMUNEMECHANISM

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 D82
Name in latin Syndroma hyperimmunoglobulini E (IgE)

Summary Statistics

Key figures

All Female Male
Number of individuals 17 11 6
Unadjusted prevalence (%) 0.00 0.00 0.00
Mean age at first event (years) 40.21 35.77 48.36

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: D3_HYPERIGESDR – Hyperimmunoglobulin E [IgE] syndrome
GWS hits:

Survival analyses between endpoints

Not a core endpoint, no data to show.

Drugs most likely to be purchased after Hyperimmunoglobulin E [IgE] syndrome

Endpoint not on priority list, no data to show.