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Up to: Idiopathic disease · Pulmonary arterial hypertension · Chronic pulmonary heart disease

Idiopathic pulmonary arterial hypertension

A sporadic form of pulmonary arterial hypertension (PAH) characterized by elevated pulmonary arterial resistance leading to right heart failure. IPAH is progressive and potentially fatal and not associated with an underlying condition or family history of PAH. The etiology is unknown.

15 trials tagged with this condition →

This condition has no sub-types.