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Summary Literature (0)
DOID:0110311 - hypertrophic cardiomyopathy 21

Disease Ontology Definition:A familial hypertrophic cardiomyopathy associated that has_material_basis_in region 7p12.1-q21 variation.

Synonyms: CMH21, cardiomyopathy familial hypertrophic 21 ,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013852 - hypertrophic cardiomyopathy 21


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)