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Pulmonary arterial hypertension associated with schistosomiasis
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.
ORPHA:275823
Classification level: Group of disorders
- PAH associated with schistosomiasis
Prevalence: Unknown
Inheritance: Not applicable
Age of onset: All ages
UMLS: C3697477
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
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