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Cardiomyopathy, Familial Hypertrophic, 15 MeSH Supplementary Concept Data 2025


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 Preferred
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