Pulmonary arterial hypertension associated

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Pulmonary arterial hypertension associated with schistosomiasis

ORPHA:275823Clinical group

Also called PAH associated with schistosomiasis

What it is

Pulmonary arterial hypertension associated with schistosomiasis (PAHS) is a form of pulmonary arterial hypertension characterized by an elevated pulmonary arterial resistance leading to right heart failure, observed as a complication of a chronic schistosomiasis.

Key facts

Age of onset
All ages
Inheritance
Not applicable
Classified as
Clinical group

Cross-references

MONDO 17155UMLS C3697477

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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