hypertrophic cardiomyopathy 15 Disease Ontology Browser

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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 familial 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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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