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DOID:0110317 - hypertrophic cardiomyopathy 11
Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the ACTC1 gene on chromosome 15q14.
Synonyms: CMH11, cardiomyopathy familial hypertrophic 11,
Echinobase Genes :
MIM:612098 - cardiomyopathy, familial hypertrophic, 11; cmh11 |
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)