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- B270ef370539a46455cde56af552e5819 hasDbXref "Orphanet:275777" @default.
- B270ef370539a46455cde56af552e5819 type Axiom @default.
- B270ef370539a46455cde56af552e5819 annotatedProperty IAO_0000115 @default.
- B270ef370539a46455cde56af552e5819 annotatedSource MONDO_0017148 @default.
- B270ef370539a46455cde56af552e5819 annotatedTarget "Heritable 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." @default.