Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Cardiomyopathy · Cardiogenetic disease
Familial cardiomyopathy
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
-
Familial hypertrophic cardiomyopathy 2 trials · 85 incl. sub-types Sub-types →
-
Familial restrictive cardiomyopathy 0 trials · 62 incl. sub-types Sub-types →
-
Familial dilated cardiomyopathy 7 trials · 60 incl. sub-types Sub-types →
-
Familial isolated arrhythmogenic right ventricular dysplasia 0 trials · 10 incl. sub-types Sub-types →
-
Left ventricular noncompaction 3 trials · 4 incl. sub-types Sub-types →
-
PRKAG2-related cardiomyopathy 2 trials · 4 incl. sub-types Sub-types →
-
Naxos disease 0 trials