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Start free with EleplanPulmonary 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
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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