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Items: 2

1.

Caused by mutation in the alpha-3 catenin gene (CTNNA3, 607667.0001)

MedGen UID:
816474
Concept ID:
C3810144
Finding
2.

Arrhythmogenic right ventricular dysplasia, familial, 13

Arrhythmogenic right ventricular cardiomyopathy/dysplasia is characterized by progressive fibrofatty myocardial replacement, primarily of the right ventricle. The main clinical features are structural and functional abnormalities of the ventricles, electrocardiographic depolarization/repolarization changes, reentrant arrhythmias, and sudden death (summary by van Hengel et al., 2013). [from OMIM]

MedGen UID:
816468
Concept ID:
C3810138
Disease or Syndrome

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