MeSH Browser

MeSH Supplementary: Cardiomyopathy, Familial Hypertrophic, 8
Unique ID: C563866
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563866
Entry Term(s): Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1
Registry Number: 0
Heading Mapped to: *Cardiomyopathy, Hypertrophic, Familial
Frequency: 0
Note: mutation in MYL3
Date of Entry: 2012/11/05

Cardiomyopathy, Familial Hypertrophic, 8 MeSH Supplementary Concept Data 2023