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Disease Ontology Browser
hypertrophic cardiomyopathy 6 (DOID:0110312)
Alliance: disease page
Synonyms: cardiomyopathy, familial hypertrophic 6; CMH6
Alt IDs: OMIM:600858
Definition: A familial 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 (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/10/2022
MGI 6.19
The Jackson Laboratory