MeSH Browser

MeSH Supplementary: Cardiomyopathy, Familial Hypertrophic, 10
Unique ID: C563865
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563865
Entry Term(s): Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2
Registry Number: 0
Heading Mapped to: *Cardiomyopathy, Hypertrophic, Familial
Frequency: 0
Note: mutation in MYL2
Date of Entry: 2012/11/05

Cardiomyopathy, Familial Hypertrophic, 10 MeSH Supplementary Concept Data 2024