Heritable pulmonary arterial hypertension
MONDO:0017148Heritable pulmonary arterial hypertension (HPAH) is a form of pulmonary arterial hypertension (PAH), occurring due to mutations in PAH predisposing genes or in a familial context. HPAH is characterized by elevated pulmonary arterial resistance leading to right heart failure. HPAH is progressive and potentially fatal.
Also known as: FPAH, HPAH, HpaH, familial pulmonary arterial hypertension, hereditary pulmonary arterial hypertension
34 clinical trials for this condition and its sub-types, 10 tagged with Heritable pulmonary arterial hypertension itself.
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Browse by category →Sub-types of Heritable pulmonary arterial hypertension
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Pulmonary hypertension, primary, 1 0 trials
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Pulmonary hypertension, primary, 5 0 trials
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Pulmonary hypertension, primary, 6 0 trials
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Pulmonary hypertension, primary, 7 0 trials