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Summary Literature (0)
MIM:603829 - VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1

Xenbase Genes: scn5a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011376 - ventricular fibrillation, paroxysmal familial, type 1
MONDO:0100234 - paroxysmal familial ventricular fibrillation