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Summary Literature (0)
MIM:107970 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007152 - arrhythmogenic right ventricular dysplasia 1
MONDO:0018084 - Uhl anomaly