Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:107970 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1

Xenbase Genes:

Human Disease Resource: OMIM

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