When people who inherit the mutation for cardiomyopathy don't develop the disease, it is known as

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Penetrance refers to the proportion of people with a particular genetic change (such as a mutation in a specific gene) who exhibit signs and symptoms of a genetic disorder. If some people with the mutation do not develop features of the disorder, the condition is said to have reduced (or incomplete) penetrance.

When People Who Inherit the Mutation for Cardiomyopathy Don't Develop