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Disease Ontology Browser
hypertrophic cardiomyopathy 6 (DOID:0110312)
Synonyms: cardiomyopathy, familial hypertrophic 6; CMH6
Alt IDs: OMIM:600858
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2).

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory