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- B54e224ed44d2a57ef322f730086ba49d hasDbXref "NCIT:C137957" @default.
- B54e224ed44d2a57ef322f730086ba49d type Axiom @default.
- B54e224ed44d2a57ef322f730086ba49d annotatedProperty IAO_0000115 @default.
- B54e224ed44d2a57ef322f730086ba49d annotatedSource MONDO_0013367 @default.
- B54e224ed44d2a57ef322f730086ba49d annotatedTarget "An autosomal dominant condition caused by mutation(s) in the KCNH2 gene, encoding potassium voltage-gated channel subfamily H member 2. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death." @default.