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Arrhythmogenic right ventricular dysplasia, familial, 15
Cardiomyopathy, familial restrictive, 5
An autosomal dominant condition caused by mutation(s) in the FLNC gene, encoding filamin-C. It is characterized by restrictive cardiomyopathy in the context of normal contractility, left ventricular wall thickness and systolic function. [from NCI]
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