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- B5aaca6f9b74ec233cc36934fddd35e7d hasDbXref "Orphanet:275813" @default.
- B5aaca6f9b74ec233cc36934fddd35e7d type Axiom @default.
- B5aaca6f9b74ec233cc36934fddd35e7d annotatedProperty IAO_0000115 @default.
- B5aaca6f9b74ec233cc36934fddd35e7d annotatedSource MONDO_0017154 @default.
- B5aaca6f9b74ec233cc36934fddd35e7d annotatedTarget "OBSOLETE. Pulmonary arterial hypertension associated with portal hypertension (PAH-PH) is a form of pulmonary arterial hypertension (PAH), characterized by an elevated pulmonary arterial resistance leading to right heart failure observed as a complication of portal hypertension." @default.