Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 (ARVD10)

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10, also known as arrhythmogenic right ventricular dysplasia 10, is related to cardiomyopathy, dilated, 1bb and acantholytic acanthoma. An important gene associated with Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 is DSG2 (Desmoglein 2), and among its related pathways/superpathways are Sertoli-Sertoli Cell Junction Dynamics and Keratinization. Affiliated tissues include heart and heart-ventricle, and related phenotypes are ventricular arrhythmia and premature ventricular contraction