Cardiomyopathy, Familial Hypertrophic, 6 MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Cardiomyopathy, Familial Hypertrophic, 6
Unique ID: C563436
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563436
Registry Number: 0
Heading Mapped to: *Cardiomyopathy, Hypertrophic, Familial
Frequency: 0
Note: mutation in PRKAG2
Date of Entry: 2012/11/05

Cardiomyopathy, Familial Hypertrophic, 6 Preferred

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