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DOID:0110310 - hypertrophic cardiomyopathy 4
Disease Ontology Definition:A hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11.
Synonyms: CMH4, cardiomyopathy, familial hypertrophic, 4,
Echinobase Genes :
MIM:115197 - cardiomyopathy, familial hypertrophic, 4; cmh4 cardiomyopathy, familial hypertrophic, 4, susceptibility to, included |
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)