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Disease Ontology Browser
hypertrophic cardiomyopathy 1 (DOID:0110307)
Synonyms: cardiomyopathy, familial hypertrophic 1; CMH1
Alt IDs: OMIM:192600
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.

Disease References using Mouse Models (2)

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
MGI 6.08
The Jackson Laboratory