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Cardiomyopathy, Familial Hypertrophic, 8 [Supplementary Concept]

mutation in MYL3

Date introduced: November 5, 2012

MeSH Unique ID: C563866

Heading Mapped to:

Entry Terms:

  • Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1

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