Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110316 - hypertrophic cardiomyopathy 10


Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.

Synonyms: CMH10, cardiomyopathy, familial hypertrophic, 10

Xenbase Genes : myl2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012112 - hypertrophic cardiomyopathy 10

OMIM:
OMIM:608758 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10

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

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