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

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

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

Xenbase Genes : myl3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012111 - hypertrophic cardiomyopathy 8


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)