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

See these related core endpoints for full statistics:

Other pulmonary heart/vessel disease

I9_PULMOTHHD

pulmonary arterial hypertension: Pulmonary arterial hypertension (PAH) is a group of diseases characterized by elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, or induced by drug or toxin (drug-or toxin-induced PAH, see these terms) or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease, see this term).

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 I27, I28
Hospital discharge: ICD-9 416|417
Hospital discharge: ICD-8 426
Cause of death: ICD-10 I27, I28
Cause of death: ICD-9 416|417
Cause of death: ICD-8 426

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

1356

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Check minimum number of events None

1356

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Include endpoints

1356

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Remove individuals based on genotype QC

1313

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I9_PULMOTHHD

Control definitions

Control exclude I9_PULMHEART

Extra metadata

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

Summary Statistics

Key figures

All Female Male
Number of individuals 1313 573 740
Unadjusted prevalence (%) 0.32 0.25 0.41
Mean age at first event (years) 65.29 62.19 67.68

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: I9_PULMOTHHD – Other pulmonary heart/vessel disease
GWS hits:

Survival analyses between endpoints

Not a core endpoint, no data to show.

Drugs most likely to be purchased after Other pulmonary heart/vessel disease

Endpoint not on priority list, no data to show.