Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 (ARVD5)

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5, also known as arrhythmogenic right ventricular dysplasia 5, is related to cardiac conduction defect and arrhythmogenic right ventricular cardiomyopathy. An important gene associated with Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 is TMEM43 (Transmembrane Protein 43), and among its related pathways/superpathways are Nervous system development and Keratinization. Affiliated tissues include heart and small intestine, and related phenotypes are sudden cardiac death and dyskinesia