|
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
MONDO:0013200 - hypertrophic cardiomyopathy 15 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

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