- OMIM ID
-
107970
- OMIM term:
- ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1
- Alternative terms:
-
ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1; ARVC1 UHL ANOMALY, INCLUDED
CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED, INCLUDED
- (∗) Location:
- 14q24.3
- (†) Associated OMIM genes:
- TGFB3
- (‡) Associated MGI genes:
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