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Summary Literature (0)
DOID:0110321 - hypertrophic cardiomyopathy 15

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the vinculin gene (VCL) on chromosome 10q22.

Synonyms: CMH15, cardiomyopathy familial hypertrophic 15


In Mondo Disease Ontology:
MONDO:0013200 - hypertrophic cardiomyopathy 15

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : vcl

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypertrophic cardiomyopathy (is_a)