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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 :
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)