Cardiomyopathy, Familial Hypertrophic, 10 [Supplementary Concept]

mutation in MYL2

Date introduced: November 5, 2012

MeSH Unique ID: C563865

Heading Mapped to:

• Cardiomyopathy, Hypertrophic, Familial

Entry Terms:

• Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2