This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
DOID EFO MESH SNOMED Endpoint Browser
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).
429209 individuals
Apply sex-specific rule None
429209
Check conditions None
429209
Check pre-conditions, main-only, mode, registry filters
2 out of 7 registries used, show all original rules.
1356
Check minimum number of events None
1356
Remove individuals based on genotype QC
1313
Control definitions
Extra metadata
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Or the full data table
List of similar endpoints to Other pulmonary heart/vessel disease based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
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 |
Not a core endpoint, no data to show.
Not a core endpoint, no data to show.
Index endpoint: I9_PULMOTHHD – Other pulmonary heart/vessel disease
GWS hits:
Not a core endpoint, no data to show.
Endpoint not on priority list, no data to show.