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Cardiomyopathy, Familial Hypertrophic, 15
MeSH Supplementary Concept Data 2023
Details
Concepts
MeSH Supplementary
Cardiomyopathy, Familial Hypertrophic, 15
Unique ID
C567681
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567681
Registry Number
0
Heading Mapped to
Vinculin
/
*deficiency
*Cardiomyopathy, Hypertrophic, Familial
Frequency
0
Date of Entry
2012/11/05
Revision Date
2013/11/06
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Cardiomyopathy, Familial Hypertrophic, 15
Preferred
Concept UI
M0567981
Registry Number
0
Terms
Cardiomyopathy, Familial Hypertrophic, 15
Preferred Term
Term UI
T810878
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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