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. 2020 Apr 3;34(3):1062–1077. doi: 10.1111/jvim.15745

Figure 1.

Figure 1

Classification of cardiomyopathy phenotypes. (adapted with permission from Clinical Small Animal Internal Medicine, Ed David Bruyette, John Wiley & Son). ARVC, arrhythmogenic right ventricular cardiomyopathy; DCM, dilated cardiomyopathy; End‐stage HCM, HCM with systolic dysfunction; HCM, hypertrophic cardiomyopathy; RCM, restrictive cardiomyopathy; TMT, transient myocardial thickening