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Echinobase
Summary Literature (0)
DOID:0110326 - hypertrophic cardiomyopathy 20

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

Synonyms: CMH20, cardiomyopathy familial hypertrophic 20,

Echinobase Genes :


OMIM:
MIM:613876 - cardiomyopathy, familial hypertrophic, 20; cmh20

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)