MeSH Browser

MeSH Supplementary: Cardiomyopathy, Familial Hypertrophic, 15
Unique ID: C567681
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567681
Registry Numbers: 0
Heading Mapped to: Vinculin / deficiency; *Cardiomyopathy, Hypertrophic, Familial
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Cardiomyopathy, Familial Hypertrophic, 15 MeSH Supplementary Concept Data 2025