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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,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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):
hypertrophic cardiomyopathy (is_a)