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Disease Ontology Browser
hypertrophic cardiomyopathy 14 (DOID:0110320)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 14; CMH14
Alt IDs: OMIM:613251
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYH6 gene.

Disease References using Mouse Models (15)

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
09/10/2019
MGI 6.14
The Jackson Laboratory