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Echinobase
Summary Literature (0)
DOID:0110314 - hypertrophic cardiomyopathy 8

Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene.

Synonyms: cardiomyopathy hypertrophic mid-left ventricular chamber type 1, cardiomyopathy, familial hypertrophic, 8,

Echinobase Genes :


OMIM:
MIM:608751 - cardiomyopathy, familial hypertrophic, 8; cmh8

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)