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Disease Ontology Browser
hypertrophic cardiomyopathy 12 (DOID:0110318)
Synonyms: cardiomyopathy familial hypertrophic 12; CMH12
Alt IDs: OMIM:612124
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.

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
04/18/2017
MGI 6.08
The Jackson Laboratory