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:0110318 - hypertrophic cardiomyopathy 12

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15.

Synonyms: CMH12, cardiomyopathy familial hypertrophic 12,

Xenbase Genes : csrp3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012804 - hypertrophic cardiomyopathy 12


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)