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- Bbff9030ea46eb9b9cdcedd0d5d4c9a61 hasDbXref "Orphanet:275803" @default.
- Bbff9030ea46eb9b9cdcedd0d5d4c9a61 type Axiom @default.
- Bbff9030ea46eb9b9cdcedd0d5d4c9a61 annotatedProperty IAO_0000115 @default.
- Bbff9030ea46eb9b9cdcedd0d5d4c9a61 annotatedSource MONDO_0017152 @default.
- Bbff9030ea46eb9b9cdcedd0d5d4c9a61 annotatedTarget "OBSOLETE. Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) is a form of pulmonary arterial hypertension (PAH), characterized by elevated pulmonary arterial resistance leading to right heart failure occurring as a common complication of congenital heart malformations with left to right cardiac shunts. Eisenmenger syndrome is the most advanced form of PAH-CHD and is defined as the complete or partial reversal of an initial left-to-right shunt to a right-to-left shunt, causing cyanosis and limited exercise capacity. PAH-CHD also includes mild to moderate systemic-to-pulmonary shunts with no cyanosis at rest, patients with small defects, and those with residual PAH following corrective cardiac surgery." @default.