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:0110317 - hypertrophic cardiomyopathy 11


Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the ACTC1 gene on chromosome 15q14.

Synonyms: CMH11, cardiomyopathy familial hypertrophic 11

In OMIM:
OMIM:612098 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11

In Mondo Disease Ontology:
MONDO:0012799 - hypertrophic cardiomyopathy 11

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

Xenbase Genes : actc1

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