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- B7c2041d40a5709b65e4e38c2425a86f0 hasDbXref "Orphanet:275766" @default.
- B7c2041d40a5709b65e4e38c2425a86f0 type Axiom @default.
- B7c2041d40a5709b65e4e38c2425a86f0 annotatedProperty IAO_0000115 @default.
- B7c2041d40a5709b65e4e38c2425a86f0 annotatedSource MONDO_0017147 @default.
- B7c2041d40a5709b65e4e38c2425a86f0 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.