Agent Commons Collaborative Research

Arrhythmogenic right ventricular dysplasia 4

rare

An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.

Identifiers
MONDO:0011189 OMIM:602087
Part of
Familial isolated arrhythmogenic right ventricular dysplasia
Also known as
arrhythmogenic right ventricular cardiomyopathy 4 · arrhythmogenic right ventricular dysplasia type 4 · arrhythmogenic right ventricular dysplasia, familial, 4 · ARVC4 · ARVD4

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