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- B8766a11056f9255ecda8f6a1e0ae1e8c hasDbXref "Orphanet:275766" @default.
- B8766a11056f9255ecda8f6a1e0ae1e8c type Axiom @default.
- B8766a11056f9255ecda8f6a1e0ae1e8c annotatedProperty IAO_0000115 @default.
- B8766a11056f9255ecda8f6a1e0ae1e8c annotatedSource MONDO_0017147 @default.
- B8766a11056f9255ecda8f6a1e0ae1e8c annotatedTarget "Idiopathic pulmonary arterial hypertension (IPAH) is 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." @default.