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Cardiomyopathy, Familial Hypertrophic, 13 MeSH Supplementary Concept Data 2022


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 Preferred
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