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MIM:107970 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0007152 - arrhythmogenic right ventricular dysplasia 1 |
MONDO:0018084 - Uhl anomaly |
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MONDO:0007152 - arrhythmogenic right ventricular dysplasia 1 |
MONDO:0018084 - Uhl anomaly |