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

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

Synonyms: cardiomyopathy familial hypertrophic 15, CMH15

Xenbase Genes : vcl

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013200 - hypertrophic cardiomyopathy 15


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)