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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: CMH20, cardiomyopathy familial hypertrophic 20,

Xenbase Genes : nexn

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


Other Model Organisms: AGR, 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)