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Idiopathic pulmonary arterial hypertension

MONDO:0001999

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.

Also known as: IPAH, idiopathic pulmonary arterial hypertension, primary pulmonary arterial hypertension, primary pulmonary hypertension

62 clinical trials for this condition and its sub-types, 15 tagged with Idiopathic pulmonary arterial hypertension itself.

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