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Disease Ontology Browser
hypertrophic cardiomyopathy 15 (DOID:0110321)
Alliance: disease page
Synonyms: cardiomyopathy familial hypertrophic 15; CMH15
Alt IDs: OMIM:613255
Definition: A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the vinculin gene (VCL) on chromosome 10q22.


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
12/05/2017
MGI 6.11
The Jackson Laboratory