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Summary Literature (0)
DOID:0110316 - hypertrophic cardiomyopathy 10

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.

Synonyms: cardiomyopathy, familial hypertrophic, 10, CMH10

Xenbase Genes : myl2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012112 - hypertrophic cardiomyopathy 10


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)