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DOID:0110316 - hypertrophic cardiomyopathy 10
Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.
Synonyms: CMH10, cardiomyopathy, familial hypertrophic, 10,
Echinobase Genes :
MIM:608758 - cardiomyopathy, familial hypertrophic, 10; cmh10 |
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)