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:0110326 - hypertrophic cardiomyopathy 20

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.

Synonyms: cardiomyopathy familial hypertrophic 20, CMH20

Xenbase Genes : nexn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013477 - hypertrophic cardiomyopathy 20

MIM:
MIM:613876 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20

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

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