Arrhythmogenic Right Ventricular Cardiomyopathy

About the Disease
Arrhythmogenic Right Ventricular Cardiomyopathy, also known as arrhythmogenic right ventricular dysplasia, is related to naxos disease and myopathy, myofibrillar, 1. An important gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy is PKP2 (Plakophilin 2), and among its related pathways/superpathways are Nervous system development and Sertoli-Sertoli Cell Junction Dynamics. The drugs Flecainide and Spironolactone have been mentioned in the context of this disorder. Affiliated tissues include heart, bone marrow and cardiac myocytes, and related phenotypes are Increased cell migration and Increased cell migration

Common Targets
CTNNA3 | CEP85L | PLN | ZBTB17 | FLNC | TMEM43 | ATP13A2 | OBSCN | AKAP6 | PLEC | TJP1 | G4233 | TNNI3 | TP63 | RYR2 | DSP | LDB3 | JUP | PPP1R13L | VCL | GAST | TTN | PNPLA2 | TRPM4 | LMNA | DSPP | Transcriptional Enhancer Factor (TEAD) (nonspecified subype) | GJA1 | HAP1 | SYNE1 | CTNNB1 | DSC2 | PERP | PTK7 | SYT10 | KCNK17 | SCN5A | PKP2 | MYH7 | WASHC5 | PLEKHM2 | PRKG1 | ALG10 | G10413 | MYBPC3 | DES | DSG2 | PPARA

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