MeSH Browser

MeSH Supplementary: Cardiomyopathy, Familial Hypertrophic, 13
Unique ID: C567686
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567686
Registry Number: 0
Heading Mapped to: Troponin C / *deficiency; *Cardiomyopathy, Hypertrophic, Familial
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Cardiomyopathy, Familial Hypertrophic, 13 MeSH Supplementary Concept Data 2024